(368433, 'HP:0007586', 'Telangiectases producing marbled skin', 'XPO:0102561', 'abnormal dermis morphology', 0.40425531914893614, 7.420886955069779, 1.732031473267709, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(368434, 'HP:0007586', 'Telangiectases producing marbled skin', 'XPO:0100054', 'abnormal blood vessel', 0.42105263157894735, 5.809304221129108, 1.5639766078650594, 'UPHENO:0002678', 'abnormal vasculature'),
(368435, 'HP:0000217', 'Xerostomia', 'XPO:0101328', 'abnormal oral epithelium', 0.40350877192982454, 7.0866363731414825, 1.6910115138695967, 'HP:0000153', 'Abnormality of the mouth'),
(368436, 'HP:0000217', 'Xerostomia', 'XPO:0100027', 'abnormal lower jaw', 0.4107142857142857, 7.0866363731414825, 1.7060430229369012, 'HP:0000153', 'Abnormality of the mouth'),
(368437, 'HP:0000217', 'Xerostomia', 'XPO:0101506', 'abnormal upper jaw', 0.4107142857142857, 7.0866363731414825, 1.7060430229369012, 'HP:0000153', 'Abnormality of the mouth'),
(368438, 'HP:0000217', 'Xerostomia', 'XPO:0101464', 'abnormal oral cavity', 0.42592592592592593, 7.0866363731414825, 1.7373491758799184, 'HP:0000153', 'Abnormality of the mouth'),
(368439, 'HP:0000217', 'Xerostomia', 'XPO:0131651', 'abnormal roof of mouth', 0.41818181818181815, 7.0866363731414825, 1.721482641014341, 'HP:0000153', 'Abnormality of the mouth'),
(368440, 'HP:0000217', 'Xerostomia', 'XPO:0100647', 'abnormal mouth', 0.4339622641509434, 7.0866363731414825, 1.7536626715827954, 'HP:0000153', 'Abnormality of the mouth'),
(368441, 'HP:0034644', 'Abnormal liver metabolite concentration', 'XPO:0141125', 'abnormally necrotic liver parenchyme', 0.5, 10.01729298920255, 2.2380005573281867, 'UPHENO:0019492', 'abnormal liver morphology'),
(368442, 'HP:0034644', 'Abnormal liver metabolite concentration', 'XPO:0130806', 'increased size of the biliary tree', 0.4090909090909091, 8.69832224767236, 1.8863733871813304, 'UPHENO:0087100', 'abnormal hepatobiliary system morphology'),
(368443, 'HP:0034644', 'Abnormal liver metabolite concentration', 'XPO:0141647', 'neoplastic liver', 0.5147058823529411, 10.01729298920255, 2.2706738265976094, 'UPHENO:0019492', 'abnormal liver morphology'),
(368444, 'HP:0034644', 'Abnormal liver metabolite concentration', 'XPO:0101674', 'abnormal hepatic vein morphology', 0.4430379746835443, 10.01729298920255, 2.1066658960898295, 'UPHENO:0019492', 'abnormal liver morphology'),
(368445, 'HP:0034644', 'Abnormal liver metabolite concentration', 'XPO:0140793', 'abnormally necrotic hepatic portal vein', 0.4069767441860465, 10.01729298920255, 2.019110023327942, 'UPHENO:0019492', 'abnormal liver morphology'),
(368446, 'HP:0034644', 'Abnormal liver metabolite concentration', 'XPO:0102825', 'abnormal bile duct morphology', 0.45, 8.69832224767236, 1.9784450994284786, 'UPHENO:0087100', 'abnormal hepatobiliary system morphology'),
(368447, 'HP:0034644', 'Abnormal liver metabolite concentration', 'XPO:0103009', 'abnormal manicotto glandulare morphology', 0.4117647058823529, 5.725717590856133, 1.5354635846428564, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(368448, 'HP:0034644', 'Abnormal liver metabolite concentration', 'XPO:0102426', 'abnormal liver morphology', 0.5384615384615384, 10.01729298920255, 2.322482937329355, 'UPHENO:0019492', 'abnormal liver morphology'),
(368449, 'HP:0034644', 'Abnormal liver metabolite concentration', 'XPO:0130151', 'increased size of the liver', 0.4117647058823529, 10.01729298920255, 2.0309524124007297, 'UPHENO:0019492', 'abnormal liver morphology'),
(368450, 'HP:0034644', 'Abnormal liver metabolite concentration', 'XPO:0129280', 'decreased size of the hepatocyte', 0.4024390243902439, 9.184143847054914, 1.9225134302959865, 'UPHENO:0086622', 'abnormal liver morphology'),
(368451, 'HP:0034644', 'Abnormal liver metabolite concentration', 'XPO:0130724', 'increased size of the liver parenchyme', 0.4861111111111111, 10.01729298920255, 2.20669830862916, 'UPHENO:0019492', 'abnormal liver morphology'),
(368452, 'HP:0034644', 'Abnormal liver metabolite concentration', 'XPO:0129330', 'decreased size of the biliary tree', 0.4090909090909091, 8.69832224767236, 1.8863733871813304, 'UPHENO:0087100', 'abnormal hepatobiliary system morphology'),
(368453, 'HP:0034644', 'Abnormal liver metabolite concentration', 'XPO:0127068', 'abnormally localised hepatic vein', 0.4861111111111111, 10.01729298920255, 2.20669830862916, 'UPHENO:0019492', 'abnormal liver morphology'),
(368454, 'HP:0034644', 'Abnormal liver metabolite concentration', 'XPO:0101788', 'abnormal foregut morphology', 0.40384615384615385, 5.725717590856133, 1.520627839767678, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(368455, 'HP:0034644', 'Abnormal liver metabolite concentration', 'XPO:0140908', 'abnormally necrotic hepatocyte', 0.44594594594594594, 9.184143847054914, 2.0237667147125786, 'UPHENO:0086622', 'abnormal liver morphology'),
(368456, 'HP:0034644', 'Abnormal liver metabolite concentration', 'XPO:0102763', 'abnormal hepatocyte morphology', 0.4782608695652174, 9.184143847054914, 2.0958093001283595, 'UPHENO:0086622', 'abnormal liver morphology'),
(368457, 'HP:0034644', 'Abnormal liver metabolite concentration', 'XPO:0101784', 'abnormal alimentary system morphology', 0.4375, 5.725717590856133, 1.582719635943005, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(368458, 'HP:0034644', 'Abnormal liver metabolite concentration', 'XPO:0102118', 'abnormal oral evagination morphology', 0.4117647058823529, 5.725717590856133, 1.5354635846428564, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(368459, 'HP:0034644', 'Abnormal liver metabolite concentration', 'XPO:0101787', 'abnormal hepatic portal vein morphology', 0.4430379746835443, 10.01729298920255, 2.1066658960898295, 'UPHENO:0019492', 'abnormal liver morphology'),
(368460, 'HP:0034644', 'Abnormal liver metabolite concentration', 'XPO:0126004', 'absent hepatic portal vein', 0.4069767441860465, 10.01729298920255, 2.019110023327942, 'UPHENO:0019492', 'abnormal liver morphology'),
(368461, 'HP:0034644', 'Abnormal liver metabolite concentration', 'XPO:0102155', 'abnormal midgut morphology', 0.40384615384615385, 5.725717590856133, 1.520627839767678, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(368462, 'HP:0034644', 'Abnormal liver metabolite concentration', 'XPO:0102211', 'abnormal biliary tree morphology', 0.4576271186440678, 8.69832224767236, 1.9951411346668921, 'UPHENO:0087100', 'abnormal hepatobiliary system morphology'),
(368463, 'HP:0034644', 'Abnormal liver metabolite concentration', 'XPO:0102655', 'abnormal ultimobranchial body morphology', 0.40384615384615385, 7.767034997756375, 1.7710695103898046, 'UPHENO:0087376', 'abnormal endocrine gland morphology'),
(368464, 'HP:0034644', 'Abnormal liver metabolite concentration', 'XPO:0107375', 'abnormal larval alimentary system morphology', 0.42, 5.725717590856133, 1.5507422055775666, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(368465, 'HP:0034644', 'Abnormal liver metabolite concentration', 'XPO:0102522', 'abnormal pharyngeal cavity morphology', 0.4375, 5.725717590856133, 1.582719635943005, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(368466, 'HP:0034644', 'Abnormal liver metabolite concentration', 'XPO:0125433', 'absent hepatic vein', 0.4666666666666667, 10.01729298920255, 2.162113948961646, 'UPHENO:0019492', 'abnormal liver morphology'),
(368467, 'HP:0034644', 'Abnormal liver metabolite concentration', 'XPO:0103168', 'abnormal liver parenchyme morphology', 0.5384615384615384, 10.01729298920255, 2.322482937329355, 'UPHENO:0019492', 'abnormal liver morphology'),
(368468, 'HP:0034644', 'Abnormal liver metabolite concentration', 'XPO:0128672', 'decreased size of the liver', 0.4430379746835443, 10.01729298920255, 2.1066658960898295, 'UPHENO:0019492', 'abnormal liver morphology'),
(368469, 'HP:0034644', 'Abnormal liver metabolite concentration', 'XPO:0141833', 'edematous alimentary system', 0.42, 5.725717590856133, 1.5507422055775666, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(368470, 'HP:0034644', 'Abnormal liver metabolite concentration', 'XPO:0140114', 'abnormally necrotic liver and biliary system', 0.4074074074074074, 8.69832224767236, 1.8824879589836343, 'UPHENO:0087100', 'abnormal hepatobiliary system morphology'),
(368471, 'HP:0034644', 'Abnormal liver metabolite concentration', 'XPO:0140388', 'abnormally necrotic biliary tree', 0.421875, 8.69832224767236, 1.9156212303680435, 'UPHENO:0087100', 'abnormal hepatobiliary system morphology'),
(368472, 'HP:0034644', 'Abnormal liver metabolite concentration', 'XPO:0140645', 'abnormally necrotic hepatic vein', 0.4069767441860465, 10.01729298920255, 2.019110023327942, 'UPHENO:0019492', 'abnormal liver morphology'),
(368473, 'HP:0034644', 'Abnormal liver metabolite concentration', 'XPO:0103088', 'abnormal capillary system of liver morphology', 0.4074074074074074, 9.184143847054914, 1.9343443938413178, 'UPHENO:0086622', 'abnormal liver morphology'),
(368474, 'HP:0034644', 'Abnormal liver metabolite concentration', 'XPO:0102125', 'abnormal liver and biliary system morphology', 0.4489795918367347, 8.69832224767236, 1.9762006913328223, 'UPHENO:0087100', 'abnormal hepatobiliary system morphology'),
(368475, 'HP:0034644', 'Abnormal liver metabolite concentration', 'XPO:0129248', 'decreased size of the liver parenchyme', 0.4861111111111111, 10.01729298920255, 2.20669830862916, 'UPHENO:0019492', 'abnormal liver morphology'),
(368476, 'HP:0034644', 'Abnormal liver metabolite concentration', 'XPO:0141005', 'abnormally necrotic bile duct', 0.4090909090909091, 8.69832224767236, 1.8863733871813304, 'UPHENO:0087100', 'abnormal hepatobiliary system morphology'),
(368477, 'HP:0034644', 'Abnormal liver metabolite concentration', 'XPO:0100042', 'abnormal hepatic vein', 0.5645161290322581, 10.01729298920255, 2.378008297219882, 'UPHENO:0019492', 'abnormal liver morphology'),
(368478, 'HP:0034644', 'Abnormal liver metabolite concentration', 'XPO:0115392', 'abnormally incomplete structure of alimentary system', 0.42857142857142855, 5.725717590856133, 1.5664861849086864, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(368479, 'HP:0034644', 'Abnormal liver metabolite concentration', 'XPO:0142061', 'abnormal digestive tract morphology', 0.42, 5.725717590856133, 1.5507422055775666, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(368480, 'HP:0034644', 'Abnormal liver metabolite concentration', 'XPO:0139877', 'abnormally necrotic liver', 0.4605263157894737, 10.01729298920255, 2.147842413796034, 'UPHENO:0019492', 'abnormal liver morphology'),
(368481, 'HP:0034644', 'Abnormal liver metabolite concentration', 'XPO:0130756', 'increased size of the hepatocyte', 0.4024390243902439, 9.184143847054914, 1.9225134302959865, 'UPHENO:0086622', 'abnormal liver morphology'),
(368482, 'HP:0034644', 'Abnormal liver metabolite concentration', 'XPO:0102367', 'abnormal hindgut morphology', 0.40384615384615385, 5.725717590856133, 1.520627839767678, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(368483, 'HP:0034644', 'Abnormal liver metabolite concentration', 'XPO:0102801', 'abnormal hepato-pancreatic duct morphology', 0.4074074074074074, 8.69832224767236, 1.8824879589836343, 'UPHENO:0087100', 'abnormal hepatobiliary system morphology'),
(368484, 'HP:0034644', 'Abnormal liver metabolite concentration', 'XPO:0101820', 'abnormal delta cell morphology', 0.43103448275862066, 7.428233084304616, 1.7893643020088765, 'UPHENO:0076812', 'abnormal endocrine system morphology'),
(368485, 'HP:0011374', 'Incomplete partition of the cochlea type I', 'XPO:0130392', 'increased size of the lagena', 0.5, 10.619592806356717, 2.3042995471896353, 'HP:0000375', 'Abnormal cochlea morphology'),
(368486, 'HP:0011374', 'Incomplete partition of the cochlea type I', 'XPO:0103015', 'abnormal anterior semicircular canal morphology', 0.47058823529411764, 9.417633977274692, 2.1051906692771607, 'UPHENO:0086712', 'abnormal petrous part of temporal bone morphology'),
(368487, 'HP:0011374', 'Incomplete partition of the cochlea type I', 'XPO:0140604', 'abnormally necrotic semicircular canal', 0.45714285714285713, 9.417633977274692, 2.074898576773574, 'UPHENO:0086712', 'abnormal petrous part of temporal bone morphology'),
(368488, 'HP:0011374', 'Incomplete partition of the cochlea type I', 'XPO:0130821', 'increased size of the lateral semicircular canal', 0.42857142857142855, 9.417633977274692, 2.0090119082283806, 'UPHENO:0086712', 'abnormal petrous part of temporal bone morphology'),
(368489, 'HP:0011374', 'Incomplete partition of the cochlea type I', 'XPO:0129236', 'decreased size of the vestibule', 0.46153846153846156, 9.417633977274692, 2.084850185793623, 'UPHENO:0086712', 'abnormal petrous part of temporal bone morphology'),
(368490, 'HP:0011374', 'Incomplete partition of the cochlea type I', 'XPO:0128537', 'decreased size of the posterior semicircular canal', 0.43636363636363634, 9.417633977274692, 2.027193382059373, 'UPHENO:0086712', 'abnormal petrous part of temporal bone morphology'),
(368491, 'HP:0011374', 'Incomplete partition of the cochlea type I', 'XPO:0101852', 'abnormal semicircular canal morphology', 0.48, 9.417633977274692, 2.1261383560558453, 'UPHENO:0086712', 'abnormal petrous part of temporal bone morphology'),
(368492, 'HP:0011374', 'Incomplete partition of the cochlea type I', 'XPO:0141053', 'abnormally necrotic posterior semicircular canal', 0.4444444444444444, 9.417633977274692, 2.0458775870053842, 'UPHENO:0086712', 'abnormal petrous part of temporal bone morphology'),
(368493, 'HP:0011374', 'Incomplete partition of the cochlea type I', 'XPO:0126148', 'absent posterior semicircular canal', 0.42105263157894735, 9.417633977274692, 1.9913110177415323, 'UPHENO:0086712', 'abnormal petrous part of temporal bone morphology'),
(368494, 'HP:0011374', 'Incomplete partition of the cochlea type I', 'XPO:0130858', 'increased size of the anterior semicircular canal', 0.42857142857142855, 9.417633977274692, 2.0090119082283806, 'UPHENO:0086712', 'abnormal petrous part of temporal bone morphology'),
(368495, 'HP:0011374', 'Incomplete partition of the cochlea type I', 'XPO:0130017', 'increased size of the posterior semicircular canal', 0.42857142857142855, 9.417633977274692, 2.0090119082283806, 'UPHENO:0086712', 'abnormal petrous part of temporal bone morphology'),
(368496, 'HP:0011374', 'Incomplete partition of the cochlea type I', 'XPO:0125956', 'absent lagena', 0.4298245614035088, 10.619592806356717, 2.1364835174361008, 'HP:0000375', 'Abnormal cochlea morphology'),
(368497, 'HP:0011374', 'Incomplete partition of the cochlea type I', 'XPO:0102835', 'abnormal vestibule morphology', 0.4948453608247423, 9.417633977274692, 2.1587664263647994, 'UPHENO:0086712', 'abnormal petrous part of temporal bone morphology'),
(368498, 'HP:0011374', 'Incomplete partition of the cochlea type I', 'XPO:0125302', 'absent semicircular canal', 0.42857142857142855, 9.417633977274692, 2.0090119082283806, 'UPHENO:0086712', 'abnormal petrous part of temporal bone morphology'),
(368499, 'HP:0011374', 'Incomplete partition of the cochlea type I', 'XPO:0125827', 'absent vestibule', 0.43636363636363634, 9.417633977274692, 2.027193382059373, 'UPHENO:0086712', 'abnormal petrous part of temporal bone morphology'),
(368500, 'HP:0011374', 'Incomplete partition of the cochlea type I', 'XPO:0130323', 'increased size of the osseous labyrinth', 0.46, 9.417633977274692, 2.081372535022589, 'UPHENO:0086712', 'abnormal petrous part of temporal bone morphology'),
(368501, 'HP:0011374', 'Incomplete partition of the cochlea type I', 'XPO:0128914', 'decreased size of the lagena', 0.5, 10.619592806356717, 2.3042995471896353, 'HP:0000375', 'Abnormal cochlea morphology'),
(368502, 'HP:0011374', 'Incomplete partition of the cochlea type I', 'XPO:0140892', 'abnormally necrotic lagena', 0.5102040816326531, 10.619592806356717, 2.327694051004117, 'HP:0000375', 'Abnormal cochlea morphology'),
(368503, 'HP:0011374', 'Incomplete partition of the cochlea type I', 'XPO:0140696', 'abnormally necrotic anterior semicircular canal', 0.4444444444444444, 9.417633977274692, 2.0458775870053842, 'UPHENO:0086712', 'abnormal petrous part of temporal bone morphology'),
(368504, 'HP:0011374', 'Incomplete partition of the cochlea type I', 'XPO:0130712', 'increased size of the vestibule', 0.46153846153846156, 9.417633977274692, 2.084850185793623, 'UPHENO:0086712', 'abnormal petrous part of temporal bone morphology'),
(368505, 'HP:0011374', 'Incomplete partition of the cochlea type I', 'XPO:0102485', 'abnormal osseous labyrinth morphology', 0.4946236559139785, 9.417633977274692, 2.158282777557035, 'UPHENO:0086712', 'abnormal petrous part of temporal bone morphology'),
(368506, 'HP:0011374', 'Incomplete partition of the cochlea type I', 'XPO:0102867', 'abnormal lagena morphology', 0.5376344086021505, 10.619592806356717, 2.3894473206248437, 'HP:0000375', 'Abnormal cochlea morphology'),
(368507, 'HP:0011374', 'Incomplete partition of the cochlea type I', 'XPO:0130018', 'increased size of the semicircular canal', 0.44036697247706424, 9.417633977274692, 2.036471203447176, 'UPHENO:0086712', 'abnormal petrous part of temporal bone morphology'),
(368508, 'HP:0011374', 'Incomplete partition of the cochlea type I', 'XPO:0128845', 'decreased size of the osseous labyrinth', 0.46, 9.417633977274692, 2.081372535022589, 'UPHENO:0086712', 'abnormal petrous part of temporal bone morphology'),
(368509, 'HP:0011374', 'Incomplete partition of the cochlea type I', 'XPO:0129346', 'decreased size of the lateral semicircular canal', 0.43636363636363634, 9.417633977274692, 2.027193382059373, 'UPHENO:0086712', 'abnormal petrous part of temporal bone morphology'),
(368510, 'HP:0011374', 'Incomplete partition of the cochlea type I', 'XPO:0128538', 'decreased size of the semicircular canal', 0.4485981308411215, 9.417633977274692, 2.0554155295587466, 'UPHENO:0086712', 'abnormal petrous part of temporal bone morphology'),
(368511, 'HP:0011374', 'Incomplete partition of the cochlea type I', 'XPO:0102134', 'abnormal posterior semicircular canal morphology', 0.47058823529411764, 9.417633977274692, 2.1051906692771607, 'UPHENO:0086712', 'abnormal petrous part of temporal bone morphology'),
(368512, 'HP:0011374', 'Incomplete partition of the cochlea type I', 'XPO:0101856', 'abnormal lateral semicircular canal morphology', 0.47058823529411764, 9.417633977274692, 2.1051906692771607, 'UPHENO:0086712', 'abnormal petrous part of temporal bone morphology'),
(368513, 'HP:0011374', 'Incomplete partition of the cochlea type I', 'XPO:0129384', 'decreased size of the anterior semicircular canal', 0.43636363636363634, 9.417633977274692, 2.027193382059373, 'UPHENO:0086712', 'abnormal petrous part of temporal bone morphology'),
(368514, 'HP:0011374', 'Incomplete partition of the cochlea type I', 'XPO:0125616', 'absent lateral semicircular canal', 0.42105263157894735, 9.417633977274692, 1.9913110177415323, 'UPHENO:0086712', 'abnormal petrous part of temporal bone morphology'),
(368515, 'HP:0011374', 'Incomplete partition of the cochlea type I', 'XPO:0140727', 'abnormally necrotic vestibule', 0.47058823529411764, 9.417633977274692, 2.1051906692771607, 'UPHENO:0086712', 'abnormal petrous part of temporal bone morphology'),
(368516, 'HP:0011374', 'Incomplete partition of the cochlea type I', 'XPO:0125301', 'absent anterior semicircular canal', 0.42105263157894735, 9.417633977274692, 1.9913110177415323, 'UPHENO:0086712', 'abnormal petrous part of temporal bone morphology'),
(368517, 'HP:0011374', 'Incomplete partition of the cochlea type I', 'XPO:0140294', 'abnormally necrotic osseous labyrinth', 0.46938775510204084, 9.417633977274692, 2.1025037624141536, 'UPHENO:0086712', 'abnormal petrous part of temporal bone morphology'),
(368518, 'HP:0011374', 'Incomplete partition of the cochlea type I', 'XPO:0141020', 'abnormally necrotic lateral semicircular canal', 0.4444444444444444, 9.417633977274692, 2.0458775870053842, 'UPHENO:0086712', 'abnormal petrous part of temporal bone morphology'),
(368519, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0102178', 'abnormal whole organism morphology', 0.4482758620689655, 2.786899518863159, 1.1177207989108764, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(368520, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0102605', 'abnormal dermal skeleton morphology', 0.5, 4.638757693672553, 1.5229507040072823, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(368521, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0103021', 'abnormal wedge region morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(368522, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0102183', 'abnormal oocyte cortex morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(368523, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0102484', 'abnormal interdigital region morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(368524, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0103145', 'abnormal basal body morphology', 0.42857142857142855, 2.786899518863159, 1.092879457252359, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(368525, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0140043', 'abnormally necrotic perichondrium', 0.45454545454545453, 4.638757693672553, 1.452076521536181, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(368526, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0102896', 'abnormal mitotic spindle morphology', 0.42857142857142855, 2.786899518863159, 1.092879457252359, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(368527, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0141505', 'abnormal tadpole morphology', 0.41935483870967744, 2.786899518863159, 1.0810641970914296, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(368528, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0128502', 'decreased size of the anatomical line', 0.41935483870967744, 2.786899518863159, 1.0810641970914296, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(368529, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0129700', 'increased size of the dermal skeleton', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(368530, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0101917', 'abnormal progenitor cell morphology', 0.4166666666666667, 2.786899518863159, 1.0775936770692605, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(368531, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0102434', 'abnormal exocrine cell morphology', 0.4166666666666667, 2.786899518863159, 1.0775936770692605, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(368532, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0103104', 'abnormal zygote cortex morphology', 0.4166666666666667, 2.786899518863159, 1.0775936770692605, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(368533, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0103179', 'abnormal lampbrush chromosome morphology', 0.42857142857142855, 2.786899518863159, 1.092879457252359, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(368534, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0128246', 'decreased size of the axial skeleton', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(368535, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0102336', 'abnormal Merkel cell morphology', 0.4166666666666667, 2.786899518863159, 1.0775936770692605, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(368536, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0141285', 'abnormal cortical actin cytoskeleton morphology', 0.4166666666666667, 2.786899518863159, 1.0775936770692605, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(368537, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0107349', 'abnormal left-right axis morphology', 0.41935483870967744, 2.786899518863159, 1.0810641970914296, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(368538, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0101969', 'abnormal zygote morphology', 0.4166666666666667, 2.786899518863159, 1.0775936770692605, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(368539, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0101642', 'abnormal multicellular anatomical structure morphology', 0.43333333333333335, 2.786899518863159, 1.0989342374200721, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(368540, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0139917', 'abnormally necrotic notochord', 0.46511627906976744, 4.638757693672553, 1.4688640910537754, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(368541, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0102526', 'abnormal nucleus morphology', 0.42857142857142855, 2.786899518863159, 1.092879457252359, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(368542, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0140567', 'abnormally necrotic postero-ventral region', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(368543, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0129487', 'increased size of the anatomical structure', 0.41935483870967744, 2.786899518863159, 1.0810641970914296, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(368544, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0101957', 'abnormal axial skeleton morphology', 0.4878048780487805, 4.638757693672553, 1.5042634845863214, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(368545, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0140720', 'abnormally necrotic bone marrow', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(368546, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0107399', 'abnormal filopodium morphology', 0.42857142857142855, 2.786899518863159, 1.092879457252359, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(368547, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0101736', 'abnormal embryonic structure morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(368548, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0101860', 'abnormal skeletal subdivision morphology', 0.5263157894736842, 4.638757693672553, 1.5625144536043167, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(368549, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0128132', 'decreased size of the perichondrium', 0.43478260869565216, 4.638757693672553, 1.4201588541997616, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(368550, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0101976', 'abnormal portion of organism substance morphology', 0.48148148148148145, 2.786899518863159, 1.1583783963292227, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(368551, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0100228', 'abnormal skeletal subdivision', 0.4117647058823529, 4.3395673355180735, 1.3367425584480601, 'UPHENO:0002964', 'abnormal skeletal system'),
(368552, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0140108', 'abnormally necrotic dermal skeleton', 0.43478260869565216, 4.638757693672553, 1.4201588541997616, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(368553, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0102009', 'abnormal connective tissue morphology', 0.4444444444444444, 3.9037819259951223, 1.3171993734173904, 'HP:0033127', 'Abnormality of the musculoskeletal system'),
(368554, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0140565', 'abnormally necrotic joint', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(368555, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0100226', 'abnormal vertebral element', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(368556, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0102979', 'abnormal hindlimb region morphology', 0.41935483870967744, 2.786899518863159, 1.0810641970914296, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(368557, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0102297', 'abnormal egg jelly morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(368558, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0141709', 'increased size of the anterior notochord', 0.45454545454545453, 4.638757693672553, 1.452076521536181, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(368559, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0101834', 'abnormal embryo morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(368560, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0129982', 'increased size of the anatomical line', 0.41935483870967744, 2.786899518863159, 1.0810641970914296, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(368561, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0140395', 'abnormally necrotic antero-dorsal region', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(368562, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0101635', 'abnormal organism subdivision morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(368563, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0102742', 'abnormal cell-free extract morphology', 0.4482758620689655, 2.786899518863159, 1.1177207989108764, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(368564, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0102832', 'abnormal joint region morphology', 0.41935483870967744, 2.786899518863159, 1.0810641970914296, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(368565, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0130188', 'increased size of the flexural organ', 0.45454545454545453, 4.638757693672553, 1.452076521536181, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(368566, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0100378', 'abnormal perichondrium', 0.42424242424242425, 4.3395673355180735, 1.3568450783281876, 'UPHENO:0002964', 'abnormal skeletal system'),
(368567, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0140559', 'abnormally necrotic articular system', 0.4878048780487805, 4.638757693672553, 1.5042634845863214, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(368568, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0139841', 'abnormally necrotic anatomical region', 0.41935483870967744, 2.786899518863159, 1.0810641970914296, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(368569, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0141723', 'abnormal posterior notochord morphology', 0.5405405405405406, 4.638757693672553, 1.5834887404633964, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(368570, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0141703', 'abnormally necrotic posterior notochord', 0.47619047619047616, 4.638757693672553, 1.4862477031377266, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(368571, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0101681', 'abnormal chondrocranium morphology', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(368572, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0129832', 'increased size of the skeletal system', 0.47619047619047616, 4.638757693672553, 1.4862477031377266, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(368573, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0102097', 'abnormal skeletal system morphology', 0.5714285714285714, 4.638757693672553, 1.628102786097549, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(368574, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0107345', 'abnormal anatomical axis morphology', 0.4482758620689655, 2.786899518863159, 1.1177207989108764, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(368575, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0102636', 'abnormal acid secreting cell morphology', 0.4166666666666667, 2.786899518863159, 1.0775936770692605, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(368576, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0102323', 'abnormal keratin accumulating cell morphology', 0.4166666666666667, 2.786899518863159, 1.0775936770692605, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(368577, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0102965', 'abnormal barrier epithelial cell morphology', 0.4166666666666667, 2.786899518863159, 1.0775936770692605, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(368578, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0141699', 'abnormally necrotic anterior notochord', 0.47619047619047616, 4.638757693672553, 1.4862477031377266, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(368579, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0101641', 'abnormal multi-tissue structure morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(368580, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0102144', 'abnormal cranial skeleton morphology', 0.47619047619047616, 4.638757693672553, 1.4862477031377266, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(368581, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0101927', 'abnormal extracellular matrix morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(368582, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0103176', 'abnormal fenestra basicranialis morphology', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(368583, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0141708', 'decreased size of the posterior notochord', 0.45454545454545453, 4.638757693672553, 1.452076521536181, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(368584, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0102165', 'abnormal melanoblast morphology', 0.4166666666666667, 2.786899518863159, 1.0775936770692605, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(368585, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0102980', 'abnormal perichordal tissue morphology', 0.4878048780487805, 4.638757693672553, 1.5042634845863214, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(368586, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0100422', 'abnormal notochord', 0.45161290322580644, 4.3395673355180735, 1.399930213666808, 'UPHENO:0002964', 'abnormal skeletal system'),
(368587, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0141704', 'decreased size of the anterior notochord', 0.45454545454545453, 4.638757693672553, 1.452076521536181, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(368588, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0102054', 'abnormal notochord morphology', 0.5405405405405406, 4.638757693672553, 1.5834887404633964, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(368589, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0102272', 'abnormal notochordal sheath morphology', 0.5405405405405406, 4.638757693672553, 1.5834887404633964, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(368590, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0102049', 'abnormal dense regular connective tissue morphology', 0.42105263157894735, 3.9037819259951223, 1.282067725609914, 'HP:0033127', 'Abnormality of the musculoskeletal system'),
(368591, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0103041', 'abnormal perivitelline space morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(368592, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0100584', 'abnormal vertebral column', 0.47619047619047616, 4.638757693672553, 1.4862477031377266, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(368593, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0141277', 'abnormal actin cytoskeleton morphology', 0.42857142857142855, 2.786899518863159, 1.092879457252359, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(368594, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0101864', 'abnormal lymphatic system morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(368595, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0102205', 'abnormal extraembryonic structure morphology', 0.41935483870967744, 2.786899518863159, 1.0810641970914296, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(368596, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0140683', 'abnormally necrotic flexural organ', 0.47619047619047616, 4.638757693672553, 1.4862477031377266, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(368597, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0139717', 'abnormally necrotic cell', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(368598, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0102588', 'abnormal centrosome morphology', 0.42857142857142855, 2.786899518863159, 1.092879457252359, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(368599, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0141713', 'increased size of the posterior notochord', 0.45454545454545453, 4.638757693672553, 1.452076521536181, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(368600, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0107348', 'abnormal dorsal-ventral axis morphology', 0.41935483870967744, 2.786899518863159, 1.0810641970914296, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(368601, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0101636', 'abnormal cell morphology', 0.4411764705882353, 2.786899518863159, 1.1088347458553505, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(368602, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0103927', 'decreased pigmentation in the whole organism', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(368603, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0102055', 'abnormal process morphology', 0.43333333333333335, 2.786899518863159, 1.0989342374200721, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(368604, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0101680', 'abnormal skeletal element morphology', 0.45454545454545453, 4.638757693672553, 1.452076521536181, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(368605, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0103043', 'abnormal marginal zone (sensu neural) morphology', 0.41935483870967744, 2.786899518863159, 1.0810641970914296, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(368606, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0129786', 'increased size of the articular system', 0.46511627906976744, 4.638757693672553, 1.4688640910537754, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(368607, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0141653', 'neoplastic skeletal element', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(368608, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0102776', 'abnormal fenestra subocularis morphology', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(368609, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0139771', 'abnormally necrotic skeletal subdivision', 0.46511627906976744, 4.638757693672553, 1.4688640910537754, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(368610, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0102773', 'abnormal Keller explant morphology', 0.4482758620689655, 2.786899518863159, 1.1177207989108764, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(368611, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0101909', 'abnormal blastocoel morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(368612, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0101716', 'abnormal anatomical group morphology', 0.43333333333333335, 2.786899518863159, 1.0989342374200721, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(368613, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0102455', 'abnormal blood morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(368614, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0139774', 'abnormally necrotic elastica externa', 0.5, 4.638757693672553, 1.5229507040072823, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(368615, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0102520', 'abnormal microtubule morphology', 0.42857142857142855, 2.786899518863159, 1.092879457252359, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(368616, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0102353', 'abnormal centromere morphology', 0.42857142857142855, 2.786899518863159, 1.092879457252359, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(368617, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0103093', 'abnormal sperm entry point morphology', 0.4166666666666667, 2.786899518863159, 1.0775936770692605, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(368618, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0102852', 'abnormal centriole morphology', 0.4166666666666667, 2.786899518863159, 1.0775936770692605, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(368619, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0102789', 'abnormal female organism morphology', 0.41935483870967744, 2.786899518863159, 1.0810641970914296, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(368620, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0129583', 'increased size of the perichordal tissue', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(368621, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0103037', 'abnormal ring structure morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(368622, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0141718', 'abnormal posterior notochord', 0.4375, 4.3395673355180735, 1.3778826906849353, 'UPHENO:0002964', 'abnormal skeletal system'),
(368623, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0102542', 'abnormal vacuolated notochordal tissue morphology', 0.4878048780487805, 4.638757693672553, 1.5042634845863214, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(368624, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0102093', 'abnormal craniofacial skeleton morphology', 0.45454545454545453, 4.638757693672553, 1.452076521536181, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(368625, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0107359', 'abnormal axial region morphology', 0.41935483870967744, 2.786899518863159, 1.0810641970914296, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(368626, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0140019', 'abnormally necrotic skeletal system', 0.5, 4.638757693672553, 1.5229507040072823, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(368627, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0141719', 'abnormal anterior notochord morphology', 0.5405405405405406, 4.638757693672553, 1.5834887404633964, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(368628, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0102929', 'abnormal barrier cell morphology', 0.4166666666666667, 2.786899518863159, 1.0775936770692605, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(368629, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0128158', 'decreased size of the skeletal subdivision', 0.4444444444444444, 4.638757693672553, 1.4358516936218344, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(368630, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0141165', 'abnormally necrotic ventral region', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(368631, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0101646', 'abnormal tissue morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(368632, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0102764', 'abnormal apoptotic cell morphology', 0.4166666666666667, 2.786899518863159, 1.0775936770692605, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(368633, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0140350', 'abnormally necrotic notochordal sheath', 0.47619047619047616, 4.638757693672553, 1.4862477031377266, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(368634, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0141091', 'abnormally necrotic posterior region', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(368635, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0102004', 'abnormal hematological system morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(368636, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0129434', 'decreased size of the notochordal sheath', 0.45454545454545453, 4.638757693672553, 1.452076521536181, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(368637, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0102461', 'abnormal postcranial axial skeleton morphology', 0.45454545454545453, 4.638757693672553, 1.452076521536181, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(368638, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0128103', 'decreased size of the perichordal tissue', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(368639, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0102360', 'abnormal cell condensation morphology', 0.43333333333333335, 2.786899518863159, 1.0989342374200721, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(368640, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0107346', 'abnormal animal-vegetal axis morphology', 0.41935483870967744, 2.786899518863159, 1.0810641970914296, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(368641, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0101740', 'abnormal cell part morphology', 0.45454545454545453, 2.786899518863159, 1.1255098882613885, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(368642, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0101921', 'abnormal chondroblast morphology', 0.4166666666666667, 2.786899518863159, 1.0775936770692605, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(368643, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0103201', 'abnormal activin-induced ectoderm morphology', 0.4482758620689655, 2.786899518863159, 1.1177207989108764, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(368644, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0102567', 'abnormal skeleton morphology', 0.5405405405405406, 4.638757693672553, 1.5834887404633964, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(368645, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0140955', 'abnormally necrotic ventro-lateral region', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(368646, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0102005', 'abnormal splanchnocranium morphology', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(368647, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0102328', 'abnormal sesamoid morphology', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(368648, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0102356', 'abnormal kinetochore morphology', 0.42857142857142855, 2.786899518863159, 1.092879457252359, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(368649, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0102704', 'abnormal mitochondrial cloud morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(368650, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0101658', 'abnormal germ cell morphology', 0.4166666666666667, 2.786899518863159, 1.0775936770692605, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(368651, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0102693', 'abnormal plasma membrane morphology', 0.42857142857142855, 2.786899518863159, 1.092879457252359, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(368652, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0102092', 'abnormal ethmoid region morphology', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(368653, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0139718', 'abnormally necrotic anatomical structure', 0.4482758620689655, 2.786899518863159, 1.1177207989108764, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(368654, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0100935', 'abnormal skeleton', 0.42424242424242425, 4.3395673355180735, 1.3568450783281876, 'UPHENO:0002964', 'abnormal skeletal system'),
(368655, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0141296', 'abnormal adherens junction morphology', 0.42857142857142855, 2.786899518863159, 1.092879457252359, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(368656, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0129612', 'increased size of the perichondrium', 0.43478260869565216, 4.638757693672553, 1.4201588541997616, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(368657, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0100693', 'abnormal vertebral centrum', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(368658, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0139889', 'abnormally necrotic cranial skeleton', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(368659, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0102133', 'abnormal urogenital system morphology', 0.4166666666666667, 2.786899518863159, 1.0775936770692605, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(368660, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0141316', 'abnormal anatomical region morphology', 0.4482758620689655, 2.786899518863159, 1.1177207989108764, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(368661, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0101713', 'abnormal anatomical entity in vitro morphology', 0.48148148148148145, 2.786899518863159, 1.1583783963292227, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(368662, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0101890', 'abnormal organ part morphology', 0.4482758620689655, 2.786899518863159, 1.1177207989108764, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(368663, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0107357', 'abnormal proximal-distal axis morphology', 0.41935483870967744, 2.786899518863159, 1.0810641970914296, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(368664, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0102181', 'abnormal mitotic cell morphology', 0.4166666666666667, 2.786899518863159, 1.0775936770692605, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(368665, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0101679', 'abnormal cartilage element morphology', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(368666, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0128890', 'decreased size of the elastica externa', 0.47619047619047616, 4.638757693672553, 1.4862477031377266, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(368667, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0140373', 'abnormally necrotic whole organism', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(368668, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0102728', 'abnormal tendon morphology', 0.46511627906976744, 4.638757693672553, 1.4688640910537754, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(368669, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0140179', 'abnormally necrotic postero-dorsal region', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(368670, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0140432', 'abnormally necrotic skeleton', 0.47619047619047616, 4.638757693672553, 1.4862477031377266, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(368671, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0129726', 'increased size of the axial skeleton', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(368672, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0107350', 'abnormal anatomical side morphology', 0.41935483870967744, 2.786899518863159, 1.0810641970914296, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(368673, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0141334', 'increased pigmentation in the whole organism', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(368674, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0103129', 'abnormal ciliary axoneme morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(368675, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0101871', 'abnormal acellular anatomical structure morphology', 0.43333333333333335, 2.786899518863159, 1.0989342374200721, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(368676, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0102010', 'abnormal perichondrium morphology', 0.5263157894736842, 4.638757693672553, 1.5625144536043167, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(368677, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0140177', 'abnormally necrotic appendicular skeleton', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(368678, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0101638', 'abnormal anatomical structure morphology', 0.48148148148148145, 2.786899518863159, 1.1583783963292227, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(368679, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0107347', 'abnormal anterior-posterior axis morphology', 0.41935483870967744, 2.786899518863159, 1.0810641970914296, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(368680, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0102601', 'abnormal disaggregated/reaggregated ectoderm treated with activin morphology', 0.4482758620689655, 2.786899518863159, 1.1177207989108764, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(368681, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0101804', 'abnormal stem cell morphology', 0.4166666666666667, 2.786899518863159, 1.0775936770692605, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(368682, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0129638', 'increased size of the skeletal subdivision', 0.4444444444444444, 4.638757693672553, 1.4358516936218344, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(368683, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0103005', 'abnormal oxygen accumulating cell morphology', 0.4166666666666667, 2.786899518863159, 1.0775936770692605, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(368684, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0103234', 'abnormal intersomitic tendon morphology', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(368685, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0115491', 'abnormally increased distribution of connective tissue', 0.43243243243243246, 3.9037819259951223, 1.2992774584144207, 'HP:0033127', 'Abnormality of the musculoskeletal system'),
(368686, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0101854', 'abnormal bone element morphology', 0.43478260869565216, 4.638757693672553, 1.4201588541997616, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(368687, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0140364', 'abnormally necrotic anterior region', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(368688, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0102130', 'abnormal endoskeleton morphology', 0.5, 4.638757693672553, 1.5229507040072823, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(368689, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0128306', 'decreased size of the articular system', 0.46511627906976744, 4.638757693672553, 1.4688640910537754, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(368690, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0102109', 'abnormal pericyte morphology', 0.4166666666666667, 2.786899518863159, 1.0775936770692605, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(368691, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0140123', 'abnormally necrotic perichondrial cell', 0.43478260869565216, 4.638757693672553, 1.4201588541997616, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(368692, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0103116', 'abnormal bone marrow morphology', 0.45454545454545453, 4.638757693672553, 1.452076521536181, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(368693, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0102217', 'abnormal elastica externa morphology', 0.5714285714285714, 4.638757693672553, 1.628102786097549, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(368694, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0103218', 'abnormal joint morphology', 0.46511627906976744, 4.638757693672553, 1.4688640910537754, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(368695, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0140269', 'abnormally necrotic anatomical line', 0.4482758620689655, 2.786899518863159, 1.1177207989108764, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(368696, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0130487', 'increased size of the endoskeleton', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(368697, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0103202', 'abnormal forelimb region morphology', 0.41935483870967744, 2.786899518863159, 1.0810641970914296, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(368698, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0102720', 'abnormal dermatocranium morphology', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(368699, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0102113', 'abnormal anatomical line morphology', 0.48148148148148145, 2.786899518863159, 1.1583783963292227, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(368700, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0102216', 'abnormal vertebral column morphology', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(368701, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0129582', 'increased size of the portion of organism substance', 0.41935483870967744, 2.786899518863159, 1.0810641970914296, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(368702, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0102347', 'abnormal ciliated cell morphology', 0.4166666666666667, 2.786899518863159, 1.0775936770692605, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(368703, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0128184', 'decreased size of the skeleton', 0.45454545454545453, 4.638757693672553, 1.452076521536181, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(368704, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0103099', 'abnormal alkali secreting cell morphology', 0.4166666666666667, 2.786899518863159, 1.0775936770692605, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(368705, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0130908', 'increased size of the notochordal sheath', 0.45454545454545453, 4.638757693672553, 1.452076521536181, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(368706, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0101702', 'abnormal anatomical system morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(368707, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0102229', 'abnormal regenerating skeletal element morphology', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(368708, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0142064', 'abnormal desmosome morphology', 0.42857142857142855, 2.786899518863159, 1.092879457252359, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(368709, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0101982', 'abnormal appendicular skeleton morphology', 0.47619047619047616, 4.638757693672553, 1.4862477031377266, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(368710, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0128102', 'decreased size of the portion of organism substance', 0.41935483870967744, 2.786899518863159, 1.0810641970914296, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(368711, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0115510', 'abnormal degeneration of whole organism', 0.43333333333333335, 2.786899518863159, 1.0989342374200721, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(368712, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0128007', 'decreased size of the anatomical structure', 0.41935483870967744, 2.786899518863159, 1.0810641970914296, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(368713, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0141714', 'abnormal anterior notochord', 0.4375, 4.3395673355180735, 1.3778826906849353, 'UPHENO:0002964', 'abnormal skeletal system'),
(368714, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0130368', 'increased size of the elastica externa', 0.47619047619047616, 4.638757693672553, 1.4862477031377266, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(368715, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0101174', 'abnormal articular system', 0.4375, 4.3395673355180735, 1.3778826906849353, 'UPHENO:0002964', 'abnormal skeletal system'),
(368716, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0103167', 'abnormal absorptive cell morphology', 0.4166666666666667, 2.786899518863159, 1.0775936770692605, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(368717, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0107285', 'abnormal flexural organ', 0.4375, 4.3395673355180735, 1.3778826906849353, 'UPHENO:0002964', 'abnormal skeletal system'),
(368718, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0101981', 'abnormal ossicle morphology', 0.43478260869565216, 4.638757693672553, 1.4201588541997616, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(368719, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0102275', 'abnormal thoracic region morphology', 0.41935483870967744, 2.786899518863159, 1.0810641970914296, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(368720, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0103355', 'decreased size of the notochord', 0.43478260869565216, 4.638757693672553, 1.4201588541997616, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(368721, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0102285', 'abnormal myoblast morphology', 0.4166666666666667, 2.786899518863159, 1.0775936770692605, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(368722, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0140144', 'abnormally necrotic portion of organism substance', 0.4482758620689655, 2.786899518863159, 1.1177207989108764, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(368723, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0100640', 'abnormal notochordal sheath', 0.4375, 4.3395673355180735, 1.3778826906849353, 'UPHENO:0002964', 'abnormal skeletal system'),
(368724, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0128709', 'decreased size of the flexural organ', 0.45454545454545453, 4.638757693672553, 1.452076521536181, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(368725, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0141289', 'abnormal spindle microtubule morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(368726, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0102741', 'abnormal egg cell-free extract morphology', 0.41935483870967744, 2.786899518863159, 1.0810641970914296, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(368727, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0103080', 'abnormal myelin accumulating cell morphology', 0.4166666666666667, 2.786899518863159, 1.0775936770692605, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(368728, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0102761', 'abnormal cartilaginous condensation morphology', 0.4444444444444444, 4.638757693672553, 1.4358516936218344, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(368729, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0103737', 'increased size of the notochord', 0.4444444444444444, 4.638757693672553, 1.4358516936218344, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(368730, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0103083', 'abnormal dorsal lymph space morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(368731, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0102703', 'abnormal endoplasmic reticulum morphology', 0.42857142857142855, 2.786899518863159, 1.092879457252359, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(368732, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0129936', 'increased size of the vacuolated notochordal tissue', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(368733, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0101694', 'abnormal anatomical space morphology', 0.4482758620689655, 2.786899518863159, 1.1177207989108764, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(368734, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0107426', 'abnormal yolk platelet morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(368735, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0102213', 'abnormal immune system morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(368736, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0140812', 'abnormally necrotic endoskeleton', 0.43478260869565216, 4.638757693672553, 1.4201588541997616, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(368737, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0139792', 'abnormally necrotic perichordal tissue', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(368738, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0129010', 'decreased size of the endoskeleton', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(368739, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0102934', 'abnormal subcortical cytoplasm morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(368740, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0141314', 'abnormal Roux spot morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(368741, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0102423', 'abnormal multiciliated cell precursor morphology', 0.4166666666666667, 2.786899518863159, 1.0775936770692605, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(368742, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0102177', 'abnormal male organism morphology', 0.41935483870967744, 2.786899518863159, 1.0810641970914296, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(368743, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0140052', 'abnormally necrotic organ part', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(368744, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0102873', 'abnormal nucleate erythrocyte morphology', 0.4166666666666667, 2.786899518863159, 1.0775936770692605, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(368745, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0101999', 'abnormal skeletal tissue morphology', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(368746, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0102164', 'abnormal mandibular mesenchyme morphology', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(368747, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0102806', 'abnormal articular system morphology', 0.5555555555555556, 4.638757693672553, 1.6053309962733116, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(368748, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0129664', 'increased size of the skeleton', 0.45454545454545453, 4.638757693672553, 1.452076521536181, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(368749, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0128352', 'decreased size of the skeletal system', 0.47619047619047616, 4.638757693672553, 1.4862477031377266, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(368750, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0139806', 'abnormally necrotic vacuolated notochordal tissue', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(368751, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0102539', 'abnormal cytoplasm morphology', 0.42857142857142855, 2.786899518863159, 1.092879457252359, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(368752, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0102386', 'abnormal electrically active cell morphology', 0.4166666666666667, 2.786899518863159, 1.0775936770692605, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(368753, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0102958', 'abnormal cementoblast morphology', 0.4166666666666667, 2.786899518863159, 1.0775936770692605, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(368754, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0141189', 'abnormally necrotic antero-ventral region', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(368755, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0103067', 'abnormal paracrine cell morphology', 0.4166666666666667, 2.786899518863159, 1.0775936770692605, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(368756, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0128456', 'decreased size of the vacuolated notochordal tissue', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(368757, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0102768', 'abnormal ooplasm morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(368758, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0139998', 'abnormally necrotic axial skeleton', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(368759, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0102514', 'abnormal perichondrial cell morphology', 0.47619047619047616, 4.638757693672553, 1.4862477031377266, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(368760, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0102024', 'abnormal cilium morphology', 0.4166666666666667, 2.786899518863159, 1.0775936770692605, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(368761, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0100465', 'abnormal skeletal system', 0.45161290322580644, 4.3395673355180735, 1.399930213666808, 'UPHENO:0002964', 'abnormal skeletal system'),
(368762, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0101764', 'abnormal cranium morphology', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(368763, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0102665', 'abnormal suspensorium morphology', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(368764, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0107372', 'abnormal flexural organ morphology', 0.5405405405405406, 4.638757693672553, 1.5834887404633964, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(368765, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0101755', 'abnormal pelvic girdle morphology', 0.43478260869565216, 4.638757693672553, 1.4201588541997616, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(368766, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0102869', 'abnormal mucus secreting cell morphology', 0.4166666666666667, 2.786899518863159, 1.0775936770692605, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(368767, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0101660', 'abnormal anatomical cluster morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(368768, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0141299', 'abnormal actin filament morphology', 0.4166666666666667, 2.786899518863159, 1.0775936770692605, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(368769, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0128220', 'decreased size of the dermal skeleton', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(368770, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0100585', 'abnormal elastica externa', 0.4666666666666667, 4.3395673355180735, 1.4230711237467255, 'UPHENO:0002964', 'abnormal skeletal system'),
(368771, 'HP:0002654', 'Multiple epiphyseal dysplasia', 'XPO:0141254', 'abnormally necrotic dorso-lateral region', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(368772, 'HP:0030411', 'Jejunal adenocarcinoma', 'XPO:0100523', 'abnormal midgut', 0.4411764705882353, 5.05060299610679, 1.4927180591674907, 'HP:0025031', 'Abnormality of the digestive system'),
(368773, 'HP:0030411', 'Jejunal adenocarcinoma', 'XPO:0101101', 'abnormal posterior foregut', 0.42857142857142855, 5.05060299610679, 1.471238981671103, 'HP:0025031', 'Abnormality of the digestive system'),
(368774, 'HP:0030411', 'Jejunal adenocarcinoma', 'XPO:0100215', 'abnormal first pancreatic bud', 0.40540540540540543, 5.05060299610679, 1.4309233924911664, 'HP:0025031', 'Abnormality of the digestive system'),
(368775, 'HP:0030411', 'Jejunal adenocarcinoma', 'XPO:0101601', 'abnormal proctodeum', 0.4166666666666667, 5.05060299610679, 1.45066119926208, 'HP:0025031', 'Abnormality of the digestive system'),
(368776, 'HP:0030411', 'Jejunal adenocarcinoma', 'XPO:0100621', 'abnormal peritoneum', 0.40540540540540543, 5.05060299610679, 1.4309233924911664, 'HP:0025031', 'Abnormality of the digestive system'),
(368777, 'HP:0030411', 'Jejunal adenocarcinoma', 'XPO:0101332', 'abnormal left spleen primordium', 0.4146341463414634, 7.4630184615845945, 1.7590970095335021, 'UPHENO:0002725', 'abnormal alimentary part of gastrointestinal system'),
(368778, 'HP:0030411', 'Jejunal adenocarcinoma', 'XPO:0100152', 'abnormal alimentary system', 0.4838709677419355, 5.05060299610679, 1.5632786569919361, 'HP:0025031', 'Abnormality of the digestive system'),
(368779, 'HP:0030411', 'Jejunal adenocarcinoma', 'XPO:0142054', 'abnormal digestive tract', 0.45454545454545453, 5.05060299610679, 1.5151662069205463, 'HP:0025031', 'Abnormality of the digestive system'),
(368780, 'HP:0030411', 'Jejunal adenocarcinoma', 'XPO:0100986', 'abnormal gut epithelium', 0.42857142857142855, 5.05060299610679, 1.471238981671103, 'HP:0025031', 'Abnormality of the digestive system'),
(368781, 'HP:0030411', 'Jejunal adenocarcinoma', 'XPO:0100735', 'abnormal hindgut', 0.4411764705882353, 5.05060299610679, 1.4927180591674907, 'HP:0025031', 'Abnormality of the digestive system'),
(368782, 'HP:0030411', 'Jejunal adenocarcinoma', 'XPO:0100493', 'abnormal liver and biliary system', 0.46875, 5.05060299610679, 1.5386585568036393, 'HP:0025031', 'Abnormality of the digestive system'),
(368783, 'HP:0030411', 'Jejunal adenocarcinoma', 'XPO:0101381', 'abnormal ventral foregut', 0.42857142857142855, 5.05060299610679, 1.471238981671103, 'HP:0025031', 'Abnormality of the digestive system'),
(368784, 'HP:0030411', 'Jejunal adenocarcinoma', 'XPO:0100492', 'abnormal gall bladder primordium', 0.40540540540540543, 5.05060299610679, 1.4309233924911664, 'HP:0025031', 'Abnormality of the digestive system'),
(368785, 'HP:0030411', 'Jejunal adenocarcinoma', 'XPO:0100718', 'abnormal ventral pancreatic bud', 0.4166666666666667, 5.05060299610679, 1.45066119926208, 'HP:0025031', 'Abnormality of the digestive system'),
(368786, 'HP:0030411', 'Jejunal adenocarcinoma', 'XPO:0115391', 'abnormally undifferentiated alimentary system', 0.46875, 5.05060299610679, 1.5386585568036393, 'HP:0025031', 'Abnormality of the digestive system'),
(368787, 'HP:0030411', 'Jejunal adenocarcinoma', 'XPO:0100486', 'abnormal oral evagination', 0.4411764705882353, 5.05060299610679, 1.4927180591674907, 'HP:0025031', 'Abnormality of the digestive system'),
(368788, 'HP:0030411', 'Jejunal adenocarcinoma', 'XPO:0101377', 'abnormal manicotto glandulare', 0.4411764705882353, 5.05060299610679, 1.4927180591674907, 'HP:0025031', 'Abnormality of the digestive system'),
(368789, 'HP:0030411', 'Jejunal adenocarcinoma', 'XPO:0100890', 'abnormal pharyngeal cavity', 0.45454545454545453, 5.05060299610679, 1.5151662069205463, 'HP:0025031', 'Abnormality of the digestive system'),
(368790, 'HP:0030411', 'Jejunal adenocarcinoma', 'XPO:0101198', 'abnormal digestive enzyme secreting cell', 0.40540540540540543, 5.05060299610679, 1.4309233924911664, 'HP:0025031', 'Abnormality of the digestive system'),
(368791, 'HP:0030411', 'Jejunal adenocarcinoma', 'XPO:0101021', 'abnormal dorsal foregut', 0.42857142857142855, 5.05060299610679, 1.471238981671103, 'HP:0025031', 'Abnormality of the digestive system'),
(368792, 'HP:0030411', 'Jejunal adenocarcinoma', 'XPO:0100156', 'abnormal foregut', 0.4411764705882353, 5.05060299610679, 1.4927180591674907, 'HP:0025031', 'Abnormality of the digestive system'),
(368793, 'HP:0030411', 'Jejunal adenocarcinoma', 'XPO:0107288', 'abnormal larval alimentary system', 0.46875, 5.05060299610679, 1.5386585568036393, 'HP:0025031', 'Abnormality of the digestive system'),
(368794, 'HP:0030411', 'Jejunal adenocarcinoma', 'XPO:0101169', 'abnormal hepato-pancreatic duct', 0.4166666666666667, 5.05060299610679, 1.45066119926208, 'HP:0025031', 'Abnormality of the digestive system'),
(368795, 'HP:0030411', 'Jejunal adenocarcinoma', 'XPO:0107304', 'abnormal hindgut endoderm', 0.40540540540540543, 5.05060299610679, 1.4309233924911664, 'HP:0025031', 'Abnormality of the digestive system'),
(368796, 'HP:0030411', 'Jejunal adenocarcinoma', 'XPO:0100462', 'abnormal anterior foregut', 0.42857142857142855, 5.05060299610679, 1.471238981671103, 'HP:0025031', 'Abnormality of the digestive system'),
(368797, 'HP:0030454', 'Abnormal electrooculogram', 'XPO:0100664', 'abnormal periocular region', 0.40540540540540543, 3.868794716113063, 1.2523698696136485, 'UPHENO:0002844', 'abnormal head'),
(368798, 'HP:0030454', 'Abnormal electrooculogram', 'XPO:0100918', 'abnormal lens', 0.4375, 6.02624522851634, 1.6237248188889333, 'HP:0000478', 'Abnormality of the eye'),
(368799, 'HP:0030454', 'Abnormal electrooculogram', 'XPO:0101578', 'abnormal pupil', 0.42857142857142855, 6.02624522851634, 1.6070707907578319, 'HP:0000478', 'Abnormality of the eye'),
(368800, 'HP:0030454', 'Abnormal electrooculogram', 'XPO:0101390', 'abnormal ciliary body', 0.42, 6.02624522851634, 1.590918915588366, 'HP:0000478', 'Abnormality of the eye'),
(368801, 'HP:0030454', 'Abnormal electrooculogram', 'XPO:0101230', 'abnormal iris', 0.42, 6.02624522851634, 1.590918915588366, 'HP:0000478', 'Abnormality of the eye'),
(368802, 'HP:0030454', 'Abnormal electrooculogram', 'XPO:0100002', 'abnormal head', 0.42857142857142855, 3.868794716113063, 1.2876547978142938, 'UPHENO:0002844', 'abnormal head'),
(368803, 'HP:0030454', 'Abnormal electrooculogram', 'XPO:0100627', 'abnormal pharyngeal region', 0.4166666666666667, 3.868794716113063, 1.2696447528267278, 'UPHENO:0002844', 'abnormal head'),
(368804, 'HP:0030454', 'Abnormal electrooculogram', 'XPO:0100564', 'abnormal central retina', 0.42857142857142855, 6.02624522851634, 1.6070707907578319, 'HP:0000478', 'Abnormality of the eye'),
(368805, 'HP:0030454', 'Abnormal electrooculogram', 'XPO:0100687', 'abnormal periotic region', 0.40540540540540543, 3.868794716113063, 1.2523698696136485, 'UPHENO:0002844', 'abnormal head'),
(368806, 'HP:0030454', 'Abnormal electrooculogram', 'XPO:0101289', 'abnormal orbital region', 0.4222222222222222, 5.757493499662858, 1.5591477479243752, 'HP:0000315', 'Abnormality of the orbital region'),
(368807, 'HP:0030454', 'Abnormal electrooculogram', 'XPO:0101416', 'abnormal cornea', 0.42857142857142855, 6.02624522851634, 1.6070707907578319, 'HP:0000478', 'Abnormality of the eye'),
(368808, 'HP:0030454', 'Abnormal electrooculogram', 'XPO:0101334', 'abnormal olfactory pit', 0.40476190476190477, 5.0624614801082695, 1.4314648271866113, 'UPHENO:0002910', 'abnormal face'),
(368809, 'HP:0030454', 'Abnormal electrooculogram', 'XPO:0101173', 'abnormal retinal layer', 0.4772727272727273, 6.02624522851634, 1.6959252623356529, 'HP:0000478', 'Abnormality of the eye'),
(368810, 'HP:0030454', 'Abnormal electrooculogram', 'XPO:0100881', 'abnormal sclera', 0.4375, 6.02624522851634, 1.6237248188889333, 'HP:0000478', 'Abnormality of the eye'),
(368811, 'HP:0030454', 'Abnormal electrooculogram', 'XPO:0142052', 'abnormal nasal region', 0.42857142857142855, 3.868794716113063, 1.2876547978142938, 'UPHENO:0002844', 'abnormal head'),
(368812, 'HP:0030454', 'Abnormal electrooculogram', 'XPO:0127803', 'abnormally localised retinal layer', 0.41509433962264153, 6.02624522851634, 1.5816005448706336, 'HP:0000478', 'Abnormality of the eye'),
(368813, 'HP:0030454', 'Abnormal electrooculogram', 'XPO:0100485', 'abnormal retina', 0.4375, 6.02624522851634, 1.6237248188889333, 'HP:0000478', 'Abnormality of the eye'),
(368814, 'HP:0030454', 'Abnormal electrooculogram', 'XPO:0100727', 'abnormal odontogenic papilla', 0.4166666666666667, 3.868794716113063, 1.2696447528267278, 'UPHENO:0002844', 'abnormal head'),
(368815, 'HP:0030454', 'Abnormal electrooculogram', 'XPO:0101554', 'abnormal peripheral retina', 0.42857142857142855, 6.02624522851634, 1.6070707907578319, 'HP:0000478', 'Abnormality of the eye'),
(368816, 'HP:0030454', 'Abnormal electrooculogram', 'XPO:0100185', 'abnormal eye', 0.40425531914893614, 5.757493499662858, 1.5256137690136826, 'HP:0000315', 'Abnormality of the orbital region'),
(368817, 'HP:0030454', 'Abnormal electrooculogram', 'XPO:0100530', 'abnormal ciliary marginal zone', 0.40384615384615385, 6.02624522851634, 1.560024345217106, 'HP:0000478', 'Abnormality of the eye'),
(368818, 'HP:0030454', 'Abnormal electrooculogram', 'XPO:0101402', 'abnormal oropharyngeal papilla', 0.40540540540540543, 3.868794716113063, 1.2523698696136485, 'UPHENO:0002844', 'abnormal head'),
(368819, 'HP:0030454', 'Abnormal electrooculogram', 'XPO:0100844', 'abnormal lens transitional zone', 0.42, 6.02624522851634, 1.590918915588366, 'HP:0000478', 'Abnormality of the eye'),
(368820, 'HP:0006109', 'Absent phalangeal crease', 'XPO:0102880', 'abnormal digit-joint region morphology', 0.5151515151515151, 6.466375519622663, 1.82514743143459, 'UPHENO:0086700', 'abnormal digit morphology'),
(368821, 'HP:0006109', 'Absent phalangeal crease', 'XPO:0129188', 'decreased size of the forelimb digit 2', 0.48936170212765956, 7.492661022682715, 1.914842382945809, 'HP:0001167', 'Abnormal finger morphology'),
(368822, 'HP:0006109', 'Absent phalangeal crease', 'XPO:0103755', 'increased size of the forelimb digit', 0.5111111111111111, 7.492661022682715, 1.9569318589266915, 'HP:0001167', 'Abnormal finger morphology'),
(368823, 'HP:0006109', 'Absent phalangeal crease', 'XPO:0103779', 'decreased size of the forelimb digit in the regenerating forelimb', 0.46938775510204084, 7.492661022682715, 1.8753568559550475, 'HP:0001167', 'Abnormal finger morphology'),
(368824, 'HP:0006109', 'Absent phalangeal crease', 'XPO:0103622', 'abnormal number of forelimb digit 5', 0.42857142857142855, 7.059765001318215, 1.739429093695262, 'UPHENO:0002708', 'abnormal manus'),
(368825, 'HP:0006109', 'Absent phalangeal crease', 'XPO:0102598', 'abnormal forelimb digit 3 morphology', 0.5609756097560976, 7.492661022682715, 2.0501707455466196, 'HP:0001167', 'Abnormal finger morphology'),
(368826, 'HP:0006109', 'Absent phalangeal crease', 'XPO:0103466', 'bifurcated forelimb digit 3', 0.46464646464646464, 7.492661022682715, 1.8658613171894334, 'HP:0001167', 'Abnormal finger morphology'),
(368827, 'HP:0006109', 'Absent phalangeal crease', 'XPO:0128213', 'decreased size of the digit', 0.4533333333333333, 6.466375519622663, 1.7121400552804105, 'UPHENO:0086700', 'abnormal digit morphology'),
(368828, 'HP:0006109', 'Absent phalangeal crease', 'XPO:0103282', 'absent forelimb digit 5', 0.44660194174757284, 7.492661022682715, 1.829272249170816, 'HP:0001167', 'Abnormal finger morphology'),
(368829, 'HP:0006109', 'Absent phalangeal crease', 'XPO:0141556', 'abnormal forelimb digit morphology in the regenerating forelimb', 0.5348837209302325, 7.492661022682715, 2.001924675776152, 'HP:0001167', 'Abnormal finger morphology'),
(368830, 'HP:0006109', 'Absent phalangeal crease', 'XPO:0140898', 'abnormally necrotic forelimb digit 5', 0.5054945054945055, 7.492661022682715, 1.9461497831613463, 'HP:0001167', 'Abnormal finger morphology'),
(368831, 'HP:0006109', 'Absent phalangeal crease', 'XPO:0129652', 'increased size of the forelimb digit 3', 0.4946236559139785, 7.492661022682715, 1.9251097079292634, 'HP:0001167', 'Abnormal finger morphology'),
(368832, 'HP:0006109', 'Absent phalangeal crease', 'XPO:0128497', 'decreased size of the digit-joint region', 0.4722222222222222, 6.466375519622663, 1.7474456265073288, 'UPHENO:0086700', 'abnormal digit morphology'),
(368833, 'HP:0006109', 'Absent phalangeal crease', 'XPO:0103632', 'abnormally increased number of digit', 0.4084507042253521, 6.393467666143939, 1.6159877384059913, 'UPHENO:0002905', 'abnormal digit'),
(368834, 'HP:0006109', 'Absent phalangeal crease', 'XPO:0125443', 'absent digit-joint region', 0.4027777777777778, 6.393467666143939, 1.6047263626124957, 'HP:0011297', 'Abnormal digit morphology'),
(368835, 'HP:0006109', 'Absent phalangeal crease', 'XPO:0127078', 'abnormally localised digit-joint region', 0.4142857142857143, 6.393467666143939, 1.6274895756443606, 'HP:0011297', 'Abnormal digit morphology'),
(368836, 'HP:0006109', 'Absent phalangeal crease', 'XPO:0103621', 'abnormal number of forelimb digit 4', 0.42857142857142855, 7.059765001318215, 1.739429093695262, 'UPHENO:0002708', 'abnormal manus'),
(368837, 'HP:0006109', 'Absent phalangeal crease', 'XPO:0103432', 'decreased size of the forelimb digit', 0.5054945054945055, 7.492661022682715, 1.9461497831613463, 'HP:0001167', 'Abnormal finger morphology'),
(368838, 'HP:0006109', 'Absent phalangeal crease', 'XPO:0129161', 'decreased size of the forelimb digit 5', 0.48936170212765956, 7.492661022682715, 1.914842382945809, 'HP:0001167', 'Abnormal finger morphology'),
(368839, 'HP:0006109', 'Absent phalangeal crease', 'XPO:0100582', 'abnormal forelimb digit', 0.4444444444444444, 7.059765001318215, 1.7713478861926604, 'UPHENO:0002708', 'abnormal manus'),
(368840, 'HP:0006109', 'Absent phalangeal crease', 'XPO:0100966', 'abnormal forelimb digit 3', 0.4383561643835616, 7.059765001318215, 1.7591735296516835, 'UPHENO:0002708', 'abnormal manus'),
(368841, 'HP:0006109', 'Absent phalangeal crease', 'XPO:0103279', 'absent forelimb digit 2', 0.44660194174757284, 7.492661022682715, 1.829272249170816, 'HP:0001167', 'Abnormal finger morphology'),
(368842, 'HP:0006109', 'Absent phalangeal crease', 'XPO:0103619', 'abnormal number of forelimb digit 2', 0.42857142857142855, 7.059765001318215, 1.739429093695262, 'UPHENO:0002708', 'abnormal manus'),
(368843, 'HP:0006109', 'Absent phalangeal crease', 'XPO:0141108', 'abnormally necrotic forelimb digit 2', 0.5054945054945055, 7.492661022682715, 1.9461497831613463, 'HP:0001167', 'Abnormal finger morphology'),
(368844, 'HP:0006109', 'Absent phalangeal crease', 'XPO:0115789', 'duplicated forelimb digit 5 in regenerating forelimb', 0.40350877192982454, 7.492661022682715, 1.7387795857293602, 'HP:0001167', 'Abnormal finger morphology'),
(368845, 'HP:0006109', 'Absent phalangeal crease', 'XPO:0115788', 'duplicated forelimb digit 4 in regenerating forelimb', 0.40350877192982454, 7.492661022682715, 1.7387795857293602, 'HP:0001167', 'Abnormal finger morphology'),
(368846, 'HP:0006109', 'Absent phalangeal crease', 'XPO:0141208', 'abnormally necrotic digit-joint region', 0.4857142857142857, 6.466375519622663, 1.7722333273792887, 'UPHENO:0086700', 'abnormal digit morphology'),
(368847, 'HP:0006109', 'Absent phalangeal crease', 'XPO:0140716', 'abnormally necrotic forelimb digit 4', 0.5054945054945055, 7.492661022682715, 1.9461497831613463, 'HP:0001167', 'Abnormal finger morphology'),
(368848, 'HP:0006109', 'Absent phalangeal crease', 'XPO:0141143', 'abnormally necrotic forelimb digit 3', 0.5054945054945055, 7.492661022682715, 1.9461497831613463, 'HP:0001167', 'Abnormal finger morphology'),
(368849, 'HP:0006109', 'Absent phalangeal crease', 'XPO:0101114', 'abnormal forelimb digit 2', 0.4383561643835616, 7.059765001318215, 1.7591735296516835, 'UPHENO:0002708', 'abnormal manus'),
(368850, 'HP:0006109', 'Absent phalangeal crease', 'XPO:0141569', 'abnormal digit-joint region morphology in the regenerating hindlimb', 0.4722222222222222, 6.466375519622663, 1.7474456265073288, 'UPHENO:0086700', 'abnormal digit morphology'),
(368851, 'HP:0006109', 'Absent phalangeal crease', 'XPO:0102529', 'abnormal forelimb digit 4 morphology', 0.5609756097560976, 7.492661022682715, 2.0501707455466196, 'HP:0001167', 'Abnormal finger morphology'),
(368852, 'HP:0006109', 'Absent phalangeal crease', 'XPO:0102214', 'abnormal forelimb digit morphology', 0.575, 7.492661022682715, 2.0756396816505895, 'HP:0001167', 'Abnormal finger morphology'),
(368853, 'HP:0006109', 'Absent phalangeal crease', 'XPO:0101810', 'abnormal digit morphology', 0.5151515151515151, 6.466375519622663, 1.82514743143459, 'UPHENO:0086700', 'abnormal digit morphology'),
(368854, 'HP:0006109', 'Absent phalangeal crease', 'XPO:0130664', 'increased size of the forelimb digit 2', 0.4946236559139785, 7.492661022682715, 1.9251097079292634, 'HP:0001167', 'Abnormal finger morphology'),
(368855, 'HP:0006109', 'Absent phalangeal crease', 'XPO:0115786', 'duplicated forelimb digit 2 in regenerating forelimb', 0.40350877192982454, 7.492661022682715, 1.7387795857293602, 'HP:0001167', 'Abnormal finger morphology'),
(368856, 'HP:0006109', 'Absent phalangeal crease', 'XPO:0100178', 'abnormal digit', 0.4666666666666667, 6.393467666143939, 1.7273153285374692, 'HP:0011297', 'Abnormal digit morphology'),
(368857, 'HP:0006109', 'Absent phalangeal crease', 'XPO:0103465', 'bifurcated forelimb digit 2', 0.46464646464646464, 7.492661022682715, 1.8658613171894334, 'HP:0001167', 'Abnormal finger morphology'),
(368858, 'HP:0006109', 'Absent phalangeal crease', 'XPO:0139962', 'abnormally necrotic digit', 0.4657534246575342, 6.466375519622663, 1.7354355486119033, 'UPHENO:0086700', 'abnormal digit morphology'),
(368859, 'HP:0006109', 'Absent phalangeal crease', 'XPO:0141568', 'abnormal digit-joint region morphology in the regenerating forelimb', 0.4722222222222222, 6.466375519622663, 1.7474456265073288, 'UPHENO:0086700', 'abnormal digit morphology'),
(368860, 'HP:0006109', 'Absent phalangeal crease', 'XPO:0115787', 'duplicated forelimb digit 3 in regenerating forelimb', 0.40350877192982454, 7.492661022682715, 1.7387795857293602, 'HP:0001167', 'Abnormal finger morphology'),
(368861, 'HP:0006109', 'Absent phalangeal crease', 'XPO:0129693', 'increased size of the digit', 0.4533333333333333, 6.466375519622663, 1.7121400552804105, 'UPHENO:0086700', 'abnormal digit morphology'),
(368862, 'HP:0006109', 'Absent phalangeal crease', 'XPO:0101155', 'abnormal forelimb digit 5', 0.4383561643835616, 7.059765001318215, 1.7591735296516835, 'UPHENO:0002708', 'abnormal manus'),
(368863, 'HP:0006109', 'Absent phalangeal crease', 'XPO:0103280', 'absent forelimb digit 3', 0.44660194174757284, 7.492661022682715, 1.829272249170816, 'HP:0001167', 'Abnormal finger morphology'),
(368864, 'HP:0006109', 'Absent phalangeal crease', 'XPO:0103609', 'abnormally increased number of forelimb digit in the regenerating forelimb', 0.42201834862385323, 7.492661022682715, 1.7782127070715896, 'HP:0001167', 'Abnormal finger morphology'),
(368865, 'HP:0006109', 'Absent phalangeal crease', 'XPO:0126603', 'abnormally localised digit', 0.4084507042253521, 6.393467666143939, 1.6159877384059913, 'UPHENO:0002905', 'abnormal digit'),
(368866, 'HP:0006109', 'Absent phalangeal crease', 'XPO:0100897', 'abnormal forelimb digit 4', 0.4383561643835616, 7.059765001318215, 1.7591735296516835, 'UPHENO:0002708', 'abnormal manus'),
(368867, 'HP:0006109', 'Absent phalangeal crease', 'XPO:0133378', 'fused forelimb digits part of regenerating forelimb', 0.4791666666666667, 7.492661022682715, 1.8947911248214497, 'HP:0001167', 'Abnormal finger morphology'),
(368868, 'HP:0006109', 'Absent phalangeal crease', 'XPO:0133358', 'fused forelimb digits', 0.5168539325842697, 7.492661022682715, 1.9678951483995373, 'HP:0001167', 'Abnormal finger morphology'),
(368869, 'HP:0006109', 'Absent phalangeal crease', 'XPO:0130624', 'increased size of the forelimb digit 4', 0.4946236559139785, 7.492661022682715, 1.9251097079292634, 'HP:0001167', 'Abnormal finger morphology'),
(368870, 'HP:0006109', 'Absent phalangeal crease', 'XPO:0103467', 'bifurcated forelimb digit 4', 0.46464646464646464, 7.492661022682715, 1.8658613171894334, 'HP:0001167', 'Abnormal finger morphology'),
(368871, 'HP:0006109', 'Absent phalangeal crease', 'XPO:0101248', 'abnormal digit-joint region', 0.4444444444444444, 6.393467666143939, 1.6856871551248356, 'UPHENO:0002905', 'abnormal digit'),
(368872, 'HP:0006109', 'Absent phalangeal crease', 'XPO:0103611', 'abnormal number of forelimb digits', 0.44, 7.059765001318215, 1.762468893507064, 'UPHENO:0002708', 'abnormal manus'),
(368873, 'HP:0006109', 'Absent phalangeal crease', 'XPO:0102787', 'abnormal forelimb digit 5 morphology', 0.5609756097560976, 7.492661022682715, 2.0501707455466196, 'HP:0001167', 'Abnormal finger morphology'),
(368874, 'HP:0006109', 'Absent phalangeal crease', 'XPO:0103634', 'abnormally increased number of forelimb digit', 0.44660194174757284, 7.492661022682715, 1.829272249170816, 'HP:0001167', 'Abnormal finger morphology'),
(368875, 'HP:0006109', 'Absent phalangeal crease', 'XPO:0129977', 'increased size of the digit-joint region', 0.4722222222222222, 6.466375519622663, 1.7474456265073288, 'UPHENO:0086700', 'abnormal digit morphology'),
(368876, 'HP:0006109', 'Absent phalangeal crease', 'XPO:0140219', 'abnormally necrotic forelimb digit', 0.5227272727272727, 7.492661022682715, 1.9790447852074682, 'HP:0001167', 'Abnormal finger morphology'),
(368877, 'HP:0006109', 'Absent phalangeal crease', 'XPO:0128172', 'decreased size of the forelimb digit 3', 0.48936170212765956, 7.492661022682715, 1.914842382945809, 'HP:0001167', 'Abnormal finger morphology'),
(368878, 'HP:0006109', 'Absent phalangeal crease', 'XPO:0125257', 'absent forelimb digit', 0.46, 7.492661022682715, 1.8565085699866966, 'HP:0001167', 'Abnormal finger morphology'),
(368879, 'HP:0006109', 'Absent phalangeal crease', 'XPO:0130637', 'increased size of the forelimb digit 5', 0.4946236559139785, 7.492661022682715, 1.9251097079292634, 'HP:0001167', 'Abnormal finger morphology'),
(368880, 'HP:0006109', 'Absent phalangeal crease', 'XPO:0103620', 'abnormal number of forelimb digit 3', 0.42857142857142855, 7.059765001318215, 1.739429093695262, 'UPHENO:0002708', 'abnormal manus'),
(368881, 'HP:0006109', 'Absent phalangeal crease', 'XPO:0103468', 'bifurcated forelimb digit 5', 0.46464646464646464, 7.492661022682715, 1.8658613171894334, 'HP:0001167', 'Abnormal finger morphology'),
(368882, 'HP:0006109', 'Absent phalangeal crease', 'XPO:0129148', 'decreased size of the forelimb digit 4', 0.48936170212765956, 7.492661022682715, 1.914842382945809, 'HP:0001167', 'Abnormal finger morphology'),
(368883, 'HP:0006109', 'Absent phalangeal crease', 'XPO:0102746', 'abnormal forelimb digit 2 morphology', 0.5609756097560976, 7.492661022682715, 2.0501707455466196, 'HP:0001167', 'Abnormal finger morphology'),
(368884, 'HP:0006109', 'Absent phalangeal crease', 'XPO:0103281', 'absent forelimb digit 4', 0.44660194174757284, 7.492661022682715, 1.829272249170816, 'HP:0001167', 'Abnormal finger morphology'),
(368885, 'HP:0011973', 'Paroxysmal lethargy', 'XPO:0100858', 'abnormal presumptive midbrain-hindbrain boundary', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(368886, 'HP:0011973', 'Paroxysmal lethargy', 'XPO:0100273', 'abnormal visual system', 0.43333333333333335, 3.94131651835137, 1.3068679445984308, 'UPHENO:0004523', 'abnormal nervous system'),
(368887, 'HP:0011973', 'Paroxysmal lethargy', 'XPO:0101501', 'abnormal parabrachial area', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(368888, 'HP:0011973', 'Paroxysmal lethargy', 'XPO:0100427', 'abnormal olfactory system', 0.43333333333333335, 3.94131651835137, 1.3068679445984308, 'UPHENO:0004523', 'abnormal nervous system'),
(368889, 'HP:0011973', 'Paroxysmal lethargy', 'XPO:0100164', 'abnormal neural nucleus', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(368890, 'HP:0011973', 'Paroxysmal lethargy', 'XPO:0100031', 'abnormal central nervous system', 0.4482758620689655, 3.94131651835137, 1.3292091859262085, 'UPHENO:0004523', 'abnormal nervous system'),
(368891, 'HP:0011973', 'Paroxysmal lethargy', 'XPO:0100032', 'abnormal nervous system', 0.4642857142857143, 3.94131651835137, 1.3527368387638634, 'UPHENO:0004523', 'abnormal nervous system'),
(368892, 'HP:0011973', 'Paroxysmal lethargy', 'XPO:0100916', 'abnormal principal cavity', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(368893, 'HP:0011973', 'Paroxysmal lethargy', 'XPO:0107253', 'abnormal enteric nervous system', 0.4482758620689655, 3.94131651835137, 1.3292091859262085, 'UPHENO:0004523', 'abnormal nervous system'),
(368894, 'HP:0011973', 'Paroxysmal lethargy', 'XPO:0100642', 'abnormal gustatory system', 0.43333333333333335, 3.94131651835137, 1.3068679445984308, 'UPHENO:0004523', 'abnormal nervous system'),
(368895, 'HP:0011973', 'Paroxysmal lethargy', 'XPO:0100537', 'abnormal medium cavity', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(368896, 'HP:0011973', 'Paroxysmal lethargy', 'XPO:0100274', 'abnormal sensory system', 0.4482758620689655, 3.94131651835137, 1.3292091859262085, 'UPHENO:0004523', 'abnormal nervous system'),
(368897, 'HP:0011973', 'Paroxysmal lethargy', 'XPO:0142051', 'abnormal cerebrospinal fluid', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(368898, 'HP:0011973', 'Paroxysmal lethargy', 'XPO:0100587', 'abnormal vestibuloauditory system', 0.43333333333333335, 3.94131651835137, 1.3068679445984308, 'UPHENO:0004523', 'abnormal nervous system'),
(368899, 'HP:0011973', 'Paroxysmal lethargy', 'XPO:0100158', 'abnormal neuromere', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(368900, 'HP:0011973', 'Paroxysmal lethargy', 'XPO:0100175', 'abnormal migrating neuroblast', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(368901, 'HP:0011973', 'Paroxysmal lethargy', 'XPO:0100196', 'abnormal neuron', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(368902, 'HP:0011973', 'Paroxysmal lethargy', 'XPO:0100702', 'abnormal glial cell', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(368903, 'HP:0011973', 'Paroxysmal lethargy', 'XPO:0100114', 'abnormal peripheral nervous system', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(368904, 'HP:0040140', 'Degeneration of the striatum', 'XPO:0101851', 'abnormal basal ganglion morphology', 0.4027777777777778, 8.02346099791745, 1.7976851200440698, 'HP:0002060', 'Abnormal cerebral morphology'),
(368905, 'HP:0040140', 'Degeneration of the striatum', 'XPO:0102442', 'abnormal medial pallium morphology', 0.4084507042253521, 8.02346099791745, 1.810300608993995, 'HP:0002060', 'Abnormal cerebral morphology'),
(368906, 'HP:0040140', 'Degeneration of the striatum', 'XPO:0100695', 'abnormal zona limitans intrathalamica', 0.40298507462686567, 6.667568321314008, 1.639185931352649, 'HP:0100547', 'Abnormal forebrain morphology'),
(368907, 'HP:0040140', 'Degeneration of the striatum', 'XPO:0101053', 'abnormal anterior hypothalamus', 0.40298507462686567, 6.667568321314008, 1.639185931352649, 'HP:0100547', 'Abnormal forebrain morphology'),
(368908, 'HP:0040140', 'Degeneration of the striatum', 'XPO:0101970', 'abnormal lateral ganglionic eminence morphology', 0.4027777777777778, 8.02346099791745, 1.7976851200440698, 'HP:0002060', 'Abnormal cerebral morphology'),
(368909, 'HP:0040140', 'Degeneration of the striatum', 'XPO:0102238', 'abnormal basal forebrain morphology', 0.4142857142857143, 8.02346099791745, 1.8231854734408677, 'HP:0002060', 'Abnormal cerebral morphology'),
(368910, 'HP:0040140', 'Degeneration of the striatum', 'XPO:0100575', 'abnormal diencephalon', 0.4153846153846154, 6.667568321314008, 1.6642131181731699, 'HP:0100547', 'Abnormal forebrain morphology'),
(368911, 'HP:0040140', 'Degeneration of the striatum', 'XPO:0100157', 'abnormal optic tract', 0.4090909090909091, 6.667568321314008, 1.6515573214369805, 'HP:0100547', 'Abnormal forebrain morphology'),
(368912, 'HP:0040140', 'Degeneration of the striatum', 'XPO:0140421', 'abnormally necrotic anterior entopeduncular region', 0.4084507042253521, 8.02346099791745, 1.810300608993995, 'HP:0002060', 'Abnormal cerebral morphology'),
(368913, 'HP:0040140', 'Degeneration of the striatum', 'XPO:0100729', 'abnormal thalamus', 0.4090909090909091, 6.667568321314008, 1.6515573214369805, 'HP:0100547', 'Abnormal forebrain morphology'),
(368914, 'HP:0040140', 'Degeneration of the striatum', 'XPO:0100263', 'abnormal prethalamus', 0.40298507462686567, 6.667568321314008, 1.639185931352649, 'HP:0100547', 'Abnormal forebrain morphology'),
(368915, 'HP:0040140', 'Degeneration of the striatum', 'XPO:0102968', 'abnormal medial ganglionic eminence morphology', 0.4027777777777778, 8.02346099791745, 1.7976851200440698, 'HP:0002060', 'Abnormal cerebral morphology'),
(368916, 'HP:0040140', 'Degeneration of the striatum', 'XPO:0107380', 'abnormal dorsal telencephalon morphology', 0.4142857142857143, 8.02346099791745, 1.8231854734408677, 'HP:0002060', 'Abnormal cerebral morphology'),
(368917, 'HP:0040140', 'Degeneration of the striatum', 'XPO:0101293', 'abnormal posterior hypothalamus', 0.40298507462686567, 6.667568321314008, 1.639185931352649, 'HP:0100547', 'Abnormal forebrain morphology'),
(368918, 'HP:0040140', 'Degeneration of the striatum', 'XPO:0101354', 'abnormal eminentia thalami', 0.4090909090909091, 6.667568321314008, 1.6515573214369805, 'HP:0100547', 'Abnormal forebrain morphology'),
(368919, 'HP:0040140', 'Degeneration of the striatum', 'XPO:0102066', 'abnormal ventral pallium morphology', 0.4084507042253521, 8.02346099791745, 1.810300608993995, 'HP:0002060', 'Abnormal cerebral morphology'),
(368920, 'HP:0040140', 'Degeneration of the striatum', 'XPO:0102357', 'abnormal subpallium morphology', 0.4142857142857143, 8.02346099791745, 1.8231854734408677, 'HP:0002060', 'Abnormal cerebral morphology'),
(368921, 'HP:0040140', 'Degeneration of the striatum', 'XPO:0103178', 'abnormal dorsal pallium morphology', 0.4084507042253521, 8.02346099791745, 1.810300608993995, 'HP:0002060', 'Abnormal cerebral morphology'),
(368922, 'HP:0040140', 'Degeneration of the striatum', 'XPO:0101797', 'abnormal lateral pallium morphology', 0.4084507042253521, 8.02346099791745, 1.810300608993995, 'HP:0002060', 'Abnormal cerebral morphology'),
(368923, 'HP:0040140', 'Degeneration of the striatum', 'XPO:0101795', 'abnormal central amygdala morphology', 0.40476190476190477, 11.189682030596343, 2.1281816210991567, 'UPHENO:0088139', 'abnormal basal ganglion morphology'),
(368924, 'HP:0040140', 'Degeneration of the striatum', 'XPO:0101986', 'abnormal amygdala morphology', 0.4027777777777778, 8.02346099791745, 1.7976851200440698, 'HP:0002060', 'Abnormal cerebral morphology'),
(368925, 'HP:0040140', 'Degeneration of the striatum', 'XPO:0102191', 'abnormal telencephalon morphology', 0.42028985507246375, 8.02346099791745, 1.8363494384224073, 'HP:0002060', 'Abnormal cerebral morphology'),
(368926, 'HP:0040140', 'Degeneration of the striatum', 'XPO:0100590', 'abnormal hypothalamus', 0.4090909090909091, 6.667568321314008, 1.6515573214369805, 'HP:0100547', 'Abnormal forebrain morphology'),
(368927, 'HP:0040140', 'Degeneration of the striatum', 'XPO:0102174', 'abnormal pallium morphology', 0.4142857142857143, 8.02346099791745, 1.8231854734408677, 'HP:0002060', 'Abnormal cerebral morphology'),
(368928, 'HP:0040140', 'Degeneration of the striatum', 'XPO:0100962', 'abnormal dorsal thalamus', 0.40298507462686567, 6.667568321314008, 1.639185931352649, 'HP:0100547', 'Abnormal forebrain morphology'),
(368929, 'HP:0040140', 'Degeneration of the striatum', 'XPO:0101186', 'abnormal optic chiasm', 0.4090909090909091, 6.667568321314008, 1.6515573214369805, 'HP:0100547', 'Abnormal forebrain morphology'),
(368930, 'HP:0040140', 'Degeneration of the striatum', 'XPO:0102826', 'abnormal anterior commissure morphology', 0.4084507042253521, 8.02346099791745, 1.810300608993995, 'HP:0002060', 'Abnormal cerebral morphology'),
(368931, 'HP:0040140', 'Degeneration of the striatum', 'XPO:0101496', 'abnormal subcommissural organ', 0.40298507462686567, 6.667568321314008, 1.639185931352649, 'HP:0100547', 'Abnormal forebrain morphology'),
(368932, 'HP:0040140', 'Degeneration of the striatum', 'XPO:0100195', 'abnormal retromammillary area', 0.40298507462686567, 6.667568321314008, 1.639185931352649, 'HP:0100547', 'Abnormal forebrain morphology'),
(368933, 'HP:0040140', 'Degeneration of the striatum', 'XPO:0102007', 'abnormal anterior entopeduncular region morphology', 0.4264705882352941, 8.02346099791745, 1.8498027277157947, 'HP:0002060', 'Abnormal cerebral morphology'),
(368934, 'HP:0040140', 'Degeneration of the striatum', 'XPO:0100763', 'abnormal pretectum', 0.4090909090909091, 6.667568321314008, 1.6515573214369805, 'HP:0100547', 'Abnormal forebrain morphology'),
(368935, 'HP:0025540', 'Abnormal T cell subset distribution', 'XPO:0102080', 'abnormal thymocyte morphology', 0.4444444444444444, 9.260765128657825, 2.028767017855133, 'HP:0002843', 'Abnormal T cell morphology'),
(368936, 'HP:0025540', 'Abnormal T cell subset distribution', 'XPO:0131005', 'abnormally increased number of thymocyte', 0.5476190476190477, 9.586341000560333, 2.2912142913482096, 'HP:0011839', 'Abnormal T cell count'),
(368937, 'HP:0025540', 'Abnormal T cell subset distribution', 'XPO:0140117', 'abnormally necrotic thymocyte', 0.4186046511627907, 9.260765128657825, 1.9689081634708983, 'HP:0002843', 'Abnormal T cell morphology'),
(368938, 'HP:0025540', 'Abnormal T cell subset distribution', 'XPO:0125284', 'absent thymocyte', 0.6133333333333333, 9.586341000560333, 2.4247932861057806, 'HP:0011839', 'Abnormal T cell count'),
(368939, 'HP:0025540', 'Abnormal T cell subset distribution', 'XPO:0131221', 'abnormally decreased number of thymocyte', 0.5411764705882353, 9.586341000560333, 2.277696684929434, 'HP:0011839', 'Abnormal T cell count'),
(368940, 'HP:0009566', 'Short distal phalanx of the 2nd finger', 'XPO:0103821', 'decreased length of forelimb digit 2 in regenerating forelimb', 0.42138364779874216, 12.379159829460056, 2.28393859935453, 'UPHENO:0046707', 'decreased length of manual digit'),
(368941, 'HP:0009566', 'Short distal phalanx of the 2nd finger', 'XPO:0103824', 'decreased length of forelimb digit 5 in regenerating forelimb', 0.42138364779874216, 12.379159829460056, 2.28393859935453, 'UPHENO:0046707', 'decreased length of manual digit'),
(368942, 'HP:0009566', 'Short distal phalanx of the 2nd finger', 'XPO:0103822', 'decreased length of forelimb digit 3 in regenerating forelimb', 0.42138364779874216, 12.379159829460056, 2.28393859935453, 'UPHENO:0046707', 'decreased length of manual digit'),
(368943, 'HP:0009566', 'Short distal phalanx of the 2nd finger', 'XPO:0103823', 'decreased length of forelimb digit 4 in regenerating forelimb', 0.42138364779874216, 12.379159829460056, 2.28393859935453, 'UPHENO:0046707', 'decreased length of manual digit'),
(368944, 'HP:0002783', 'Recurrent lower respiratory tract infections', 'XPO:0101036', 'abnormal pharynx', 0.43636363636363634, 7.241224942262181, 1.777584666769093, 'HP:0012252', 'Abnormal respiratory system morphology'),
(368945, 'HP:0002783', 'Recurrent lower respiratory tract infections', 'XPO:0141593', 'edematous lung', 0.4153846153846154, 9.627087342903641, 1.9997359758743471, 'UPHENO:0019970', 'abnormal lung morphology'),
(368946, 'HP:0002783', 'Recurrent lower respiratory tract infections', 'XPO:0102932', 'abnormal lung morphology', 0.43548387096774194, 9.627087342903641, 2.0475451795338317, 'HP:0002088', 'Abnormal lung morphology'),
(368947, 'HP:0002783', 'Recurrent lower respiratory tract infections', 'XPO:0100586', 'abnormal thyroid primordium', 0.4067796610169492, 7.241224942262181, 1.7162700916117157, 'HP:0012252', 'Abnormal respiratory system morphology'),
(368948, 'HP:0002783', 'Recurrent lower respiratory tract infections', 'XPO:0102436', 'abnormal larynx morphology', 0.4067796610169492, 7.241224942262181, 1.7162700916117157, 'HP:0012252', 'Abnormal respiratory system morphology'),
(368949, 'HP:0002783', 'Recurrent lower respiratory tract infections', 'XPO:0101548', 'abnormal pulmonary vein', 0.4426229508196721, 9.627087342903641, 2.064260111399415, 'HP:0002088', 'Abnormal lung morphology'),
(368950, 'HP:0002783', 'Recurrent lower respiratory tract infections', 'XPO:0139850', 'abnormally necrotic respiratory system', 0.47058823529411764, 7.241224942262181, 1.8459781328463531, 'HP:0012252', 'Abnormal respiratory system morphology'),
(368951, 'HP:0002783', 'Recurrent lower respiratory tract infections', 'XPO:0141648', 'neoplastic lung', 0.4153846153846154, 9.627087342903641, 1.9997359758743471, 'UPHENO:0019970', 'abnormal lung morphology'),
(368952, 'HP:0002783', 'Recurrent lower respiratory tract infections', 'XPO:0100804', 'abnormal larynx', 0.47058823529411764, 7.241224942262181, 1.8459781328463531, 'HP:0012252', 'Abnormal respiratory system morphology'),
(368953, 'HP:0002783', 'Recurrent lower respiratory tract infections', 'XPO:0141614', 'metaplastic larynx', 0.4444444444444444, 7.241224942262181, 1.793968281927239, 'HP:0012252', 'Abnormal respiratory system morphology'),
(368954, 'HP:0002783', 'Recurrent lower respiratory tract infections', 'XPO:0100210', 'abnormal pulmonary artery', 0.4426229508196721, 9.627087342903641, 2.064260111399415, 'UPHENO:0019970', 'abnormal lung morphology'),
(368955, 'HP:0002783', 'Recurrent lower respiratory tract infections', 'XPO:0101949', 'abnormal respiratory system morphology', 0.5217391304347826, 7.241224942262181, 1.9437156182576012, 'HP:0012252', 'Abnormal respiratory system morphology'),
(368956, 'HP:0002783', 'Recurrent lower respiratory tract infections', 'XPO:0101329', 'abnormal pharyngeal epithelium', 0.42857142857142855, 7.241224942262181, 1.7616418813460253, 'HP:0012252', 'Abnormal respiratory system morphology'),
(368957, 'HP:0002783', 'Recurrent lower respiratory tract infections', 'XPO:0128535', 'decreased size of the respiratory system', 0.4528301886792453, 7.241224942262181, 1.810813424092455, 'HP:0012252', 'Abnormal respiratory system morphology'),
(368958, 'HP:0002783', 'Recurrent lower respiratory tract infections', 'XPO:0130015', 'increased size of the respiratory system', 0.4528301886792453, 7.241224942262181, 1.810813424092455, 'HP:0012252', 'Abnormal respiratory system morphology'),
(368959, 'HP:0002783', 'Recurrent lower respiratory tract infections', 'XPO:0100875', 'abnormal oropharynx', 0.41379310344827586, 7.241224942262181, 1.7310022939400542, 'HP:0012252', 'Abnormal respiratory system morphology'),
(368960, 'HP:0100376', 'Aplasia/hypoplasia of the proximal phalanx of the 4th toe', 'XPO:0103838', 'abnormally decreased number of hindlimb digit in the regenerating hindlimb', 0.4573643410852713, 11.012377498788434, 2.2442523874367697, 'HP:0010760', 'Absent toe'),
(368961, 'HP:0100376', 'Aplasia/hypoplasia of the proximal phalanx of the 4th toe', 'XPO:0103289', 'absent hindlimb digit', 0.5175438596491229, 11.012377498788434, 2.3873391788005573, 'HP:0010760', 'Absent toe'),
(368962, 'HP:0100376', 'Aplasia/hypoplasia of the proximal phalanx of the 4th toe', 'XPO:0141524', 'absent hindlimb digit 1 in the regenerating hindlimb', 0.47580645161290325, 11.012377498788434, 2.289052262732396, 'HP:0010760', 'Absent toe'),
(368963, 'HP:0100376', 'Aplasia/hypoplasia of the proximal phalanx of the 4th toe', 'XPO:0103293', 'absent hindlimb digit 5', 0.5042735042735043, 11.012377498788434, 2.3565335116854866, 'HP:0010760', 'Absent toe'),
(368964, 'HP:0100376', 'Aplasia/hypoplasia of the proximal phalanx of the 4th toe', 'XPO:0103292', 'absent hindlimb digit 4', 0.5042735042735043, 11.012377498788434, 2.3565335116854866, 'HP:0010760', 'Absent toe'),
(368965, 'HP:0100376', 'Aplasia/hypoplasia of the proximal phalanx of the 4th toe', 'XPO:0141528', 'absent hindlimb digit 2 in the regenerating hindlimb', 0.47580645161290325, 11.012377498788434, 2.289052262732396, 'HP:0010760', 'Absent toe'),
(368966, 'HP:0100376', 'Aplasia/hypoplasia of the proximal phalanx of the 4th toe', 'XPO:0103908', 'absent hindlimb digit 1', 0.5042735042735043, 11.012377498788434, 2.3565335116854866, 'HP:0010760', 'Absent toe'),
(368967, 'HP:0100376', 'Aplasia/hypoplasia of the proximal phalanx of the 4th toe', 'XPO:0103290', 'absent hindlimb digit 2', 0.5042735042735043, 11.012377498788434, 2.3565335116854866, 'HP:0010760', 'Absent toe'),
(368968, 'HP:0100376', 'Aplasia/hypoplasia of the proximal phalanx of the 4th toe', 'XPO:0103589', 'abnormally decreased number of hindlimb digit', 0.4796747967479675, 11.012377498788434, 2.2983385169385366, 'HP:0010760', 'Absent toe'),
(368969, 'HP:0100376', 'Aplasia/hypoplasia of the proximal phalanx of the 4th toe', 'XPO:0141529', 'absent hindlimb digit 3 in the regenerating hindlimb', 0.47580645161290325, 11.012377498788434, 2.289052262732396, 'HP:0010760', 'Absent toe'),
(368970, 'HP:0100376', 'Aplasia/hypoplasia of the proximal phalanx of the 4th toe', 'XPO:0103291', 'absent hindlimb digit 3', 0.5042735042735043, 11.012377498788434, 2.3565335116854866, 'HP:0010760', 'Absent toe'),
(368971, 'HP:0007495', 'Prematurely aged appearance', 'XPO:0100289', 'abnormal chondroblast', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(368972, 'HP:0007495', 'Prematurely aged appearance', 'XPO:0101515', 'abnormal neuromast mantle cell', 0.4411764705882353, 6.8660902472206855, 1.740447489012273, 'HP:0000951', 'Abnormality of the skin'),
(368973, 'HP:0007495', 'Prematurely aged appearance', 'XPO:0100754', 'abnormal electrically active cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(368974, 'HP:0007495', 'Prematurely aged appearance', 'XPO:0100081', 'abnormal anatomical entity in vitro', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(368975, 'HP:0007495', 'Prematurely aged appearance', 'XPO:0100004', 'abnormal cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(368976, 'HP:0007495', 'Prematurely aged appearance', 'XPO:0102727', 'abnormal skin seromucous gland morphology', 0.43902439024390244, 7.420886955069779, 1.8049793268950312, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(368977, 'HP:0007495', 'Prematurely aged appearance', 'XPO:0101254', 'abnormal stratum compactum', 0.4411764705882353, 6.8660902472206855, 1.740447489012273, 'HP:0000951', 'Abnormality of the skin'),
(368978, 'HP:0007495', 'Prematurely aged appearance', 'XPO:0103147', 'abnormal neuromast mantle cell morphology', 0.42857142857142855, 7.420886955069779, 1.7833620281931915, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(368979, 'HP:0007495', 'Prematurely aged appearance', 'XPO:0100852', 'abnormal interdigital region', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(368980, 'HP:0007495', 'Prematurely aged appearance', 'XPO:0100285', 'abnormal progenitor cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(368981, 'HP:0007495', 'Prematurely aged appearance', 'XPO:0101467', 'abnormal alkali secreting cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(368982, 'HP:0007495', 'Prematurely aged appearance', 'XPO:0100715', 'abnormal ciliated cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(368983, 'HP:0007495', 'Prematurely aged appearance', 'XPO:0100481', 'abnormal anatomical line', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(368984, 'HP:0007495', 'Prematurely aged appearance', 'XPO:0100533', 'abnormal melanoblast', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(368985, 'HP:0007495', 'Prematurely aged appearance', 'XPO:0101208', 'abnormal stratum spongiosum', 0.4411764705882353, 6.8660902472206855, 1.740447489012273, 'HP:0000951', 'Abnormality of the skin'),
(368986, 'HP:0007495', 'Prematurely aged appearance', 'XPO:0100653', 'abnormal myoblast', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(368987, 'HP:0007495', 'Prematurely aged appearance', 'XPO:0101591', 'abnormal xanthophore', 0.42857142857142855, 6.8660902472206855, 1.7154037734456928, 'HP:0000951', 'Abnormality of the skin'),
(368988, 'HP:0007495', 'Prematurely aged appearance', 'XPO:0100172', 'abnormal stem cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(368989, 'HP:0007495', 'Prematurely aged appearance', 'XPO:0100477', 'abnormal pericyte', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(368990, 'HP:0007495', 'Prematurely aged appearance', 'XPO:0101241', 'abnormal nucleate erythrocyte', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(368991, 'HP:0007495', 'Prematurely aged appearance', 'XPO:0102626', 'abnormal granular gland morphology', 0.43902439024390244, 7.420886955069779, 1.8049793268950312, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(368992, 'HP:0007495', 'Prematurely aged appearance', 'XPO:0101297', 'abnormal barrier cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(368993, 'HP:0007495', 'Prematurely aged appearance', 'XPO:0102945', 'abnormal Eberth-Kastschenko layer morphology', 0.42857142857142855, 7.420886955069779, 1.7833620281931915, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(368994, 'HP:0007495', 'Prematurely aged appearance', 'XPO:0100108', 'abnormal cell part', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(368995, 'HP:0007495', 'Prematurely aged appearance', 'XPO:0100791', 'abnormal multiciliated cell precursor', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(368996, 'HP:0007495', 'Prematurely aged appearance', 'XPO:0100544', 'abnormal neuromast support cell', 0.4411764705882353, 6.8660902472206855, 1.740447489012273, 'HP:0000951', 'Abnormality of the skin'),
(368997, 'HP:0007495', 'Prematurely aged appearance', 'XPO:0103223', 'abnormal xanthophore morphology', 0.4090909090909091, 7.420886955069779, 1.7423597190908553, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(368998, 'HP:0007495', 'Prematurely aged appearance', 'XPO:0101333', 'abnormal barrier epithelial cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(368999, 'HP:0007495', 'Prematurely aged appearance', 'XPO:0101529', 'abnormal skin mucous gland', 0.4411764705882353, 6.8660902472206855, 1.740447489012273, 'HP:0000951', 'Abnormality of the skin'),
(369000, 'HP:0007495', 'Prematurely aged appearance', 'XPO:0102176', 'abnormal neuromast support cell morphology', 0.42857142857142855, 7.420886955069779, 1.7833620281931915, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(369001, 'HP:0007495', 'Prematurely aged appearance', 'XPO:0102954', 'abnormal iridophore morphology', 0.4090909090909091, 7.420886955069779, 1.7423597190908553, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(369002, 'HP:0007495', 'Prematurely aged appearance', 'XPO:0100344', 'abnormal portion of organism substance', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369003, 'HP:0007495', 'Prematurely aged appearance', 'XPO:0101132', 'abnormal apoptotic cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(369004, 'HP:0007495', 'Prematurely aged appearance', 'XPO:0101014', 'abnormal goblet cell', 0.40540540540540543, 6.8660902472206855, 1.6683974647021622, 'HP:0000951', 'Abnormality of the skin'),
(369005, 'HP:0007495', 'Prematurely aged appearance', 'XPO:0102615', 'abnormal skin gland morphology', 0.46153846153846156, 7.420886955069779, 1.8506822386605823, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(369006, 'HP:0007495', 'Prematurely aged appearance', 'XPO:0101373', 'abnormal oxygen accumulating cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(369007, 'HP:0007495', 'Prematurely aged appearance', 'XPO:0102910', 'abnormal pigment cell morphology', 0.42857142857142855, 7.420886955069779, 1.7833620281931915, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(369008, 'HP:0007495', 'Prematurely aged appearance', 'XPO:0101278', 'abnormal pigment cell', 0.4411764705882353, 6.8660902472206855, 1.740447489012273, 'HP:0000951', 'Abnormality of the skin'),
(369009, 'HP:0007495', 'Prematurely aged appearance', 'XPO:0101004', 'abnormal acid secreting cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(369010, 'HP:0007495', 'Prematurely aged appearance', 'XPO:0100337', 'abnormal zygote', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(369011, 'HP:0007495', 'Prematurely aged appearance', 'XPO:0102561', 'abnormal dermis morphology', 0.45, 7.420886955069779, 1.8274022900777487, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(369012, 'HP:0007495', 'Prematurely aged appearance', 'XPO:0101322', 'abnormal iridophore', 0.42857142857142855, 6.8660902472206855, 1.7154037734456928, 'HP:0000951', 'Abnormality of the skin'),
(369013, 'HP:0007495', 'Prematurely aged appearance', 'XPO:0100026', 'abnormal germ cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(369014, 'HP:0007495', 'Prematurely aged appearance', 'XPO:0100691', 'abnormal keratin accumulating cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(369015, 'HP:0007495', 'Prematurely aged appearance', 'XPO:0101237', 'abnormal mucus secreting cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(369016, 'HP:0007495', 'Prematurely aged appearance', 'XPO:0100549', 'abnormal mitotic cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(369017, 'HP:0007495', 'Prematurely aged appearance', 'XPO:0101387', 'abnormal melanophore', 0.42857142857142855, 6.8660902472206855, 1.7154037734456928, 'HP:0000951', 'Abnormality of the skin'),
(369018, 'HP:0007495', 'Prematurely aged appearance', 'XPO:0100994', 'abnormal granular gland', 0.46875, 6.8660902472206855, 1.7940122082596586, 'HP:0000951', 'Abnormality of the skin'),
(369019, 'HP:0007495', 'Prematurely aged appearance', 'XPO:0100006', 'abnormal anatomical structure', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369020, 'HP:0007495', 'Prematurely aged appearance', 'XPO:0101326', 'abnormal cementoblast', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(369021, 'HP:0007495', 'Prematurely aged appearance', 'XPO:0100983', 'abnormal skin gland', 0.4838709677419355, 6.8660902472206855, 1.8227182263109507, 'HP:0000951', 'Abnormality of the skin'),
(369022, 'HP:0007495', 'Prematurely aged appearance', 'XPO:0102886', 'abnormal stratum compactum morphology', 0.42857142857142855, 7.420886955069779, 1.7833620281931915, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(369023, 'HP:0007495', 'Prematurely aged appearance', 'XPO:0100929', 'abnormal dermis', 0.46875, 6.8660902472206855, 1.7940122082596586, 'HP:0000951', 'Abnormality of the skin'),
(369024, 'HP:0007495', 'Prematurely aged appearance', 'XPO:0103019', 'abnormal melanophore morphology', 0.4090909090909091, 7.420886955069779, 1.7423597190908553, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(369025, 'HP:0007495', 'Prematurely aged appearance', 'XPO:0100507', 'abnormal skin', 0.5, 6.8660902472206855, 1.8528478414619864, 'HP:0000951', 'Abnormality of the skin'),
(369026, 'HP:0007495', 'Prematurely aged appearance', 'XPO:0101448', 'abnormal myelin accumulating cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(369027, 'HP:0007495', 'Prematurely aged appearance', 'XPO:0100802', 'abnormal exocrine cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(369028, 'HP:0007495', 'Prematurely aged appearance', 'XPO:0102840', 'abnormal stratum spongiosum morphology', 0.42857142857142855, 7.420886955069779, 1.7833620281931915, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(369029, 'HP:0007495', 'Prematurely aged appearance', 'XPO:0102139', 'abnormal skin morphology', 0.46153846153846156, 7.420886955069779, 1.8506822386605823, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(369030, 'HP:0007495', 'Prematurely aged appearance', 'XPO:0101313', 'abnormal Eberth-Kastschenko layer', 0.4411764705882353, 6.8660902472206855, 1.740447489012273, 'HP:0000951', 'Abnormality of the skin'),
(369031, 'HP:0007495', 'Prematurely aged appearance', 'XPO:0101095', 'abnormal skin seromucous gland', 0.46875, 6.8660902472206855, 1.7940122082596586, 'HP:0000951', 'Abnormality of the skin'),
(369032, 'HP:0007495', 'Prematurely aged appearance', 'XPO:0100704', 'abnormal Merkel cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(369033, 'HP:0007495', 'Prematurely aged appearance', 'XPO:0100638', 'abnormal polar body', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(369034, 'HP:0007495', 'Prematurely aged appearance', 'XPO:0101435', 'abnormal paracrine cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(369035, 'HP:0007495', 'Prematurely aged appearance', 'XPO:0101535', 'abnormal absorptive cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(369036, 'HP:0008003', 'Jerky ocular pursuit movements', 'XPO:0101173', 'abnormal retinal layer', 0.4107142857142857, 6.02624522851634, 1.5732339319278652, 'HP:0000478', 'Abnormality of the eye'),
(369037, 'HP:0008821', 'Hypoplastic inferior ilia', 'XPO:0129382', 'decreased size of the iliac process', 0.41836734693877553, 10.417633977274692, 2.087677630394994, 'UPHENO:0076728', 'abnormal pelvic girdle bone/zone morphology'),
(369038, 'HP:0004232', 'Accessory carpal bones', 'XPO:0133362', 'fused carpi', 0.40404040404040403, 11.022225284744781, 2.1103138054499477, 'HP:0003019', 'Abnormality of the wrist'),
(369039, 'HP:0004232', 'Accessory carpal bones', 'XPO:0100970', 'abnormal carpus', 0.42168674698795183, 11.022225284744781, 2.1559049897647107, 'HP:0003019', 'Abnormality of the wrist'),
(369040, 'HP:0004232', 'Accessory carpal bones', 'XPO:0102602', 'abnormal carpus morphology', 0.4166666666666667, 11.022225284744781, 2.1430338001636042, 'HP:0003019', 'Abnormality of the wrist'),
(369041, 'HP:0000505', 'Visual impairment', 'XPO:0101173', 'abnormal retinal layer', 0.42857142857142855, 6.02624522851634, 1.6070707907578319, 'HP:0000478', 'Abnormality of the eye'),
(369042, 'HP:0033751', 'Elevated functional residual capacity', 'XPO:0100804', 'abnormal larynx', 0.42857142857142855, 7.032762738978795, 1.7360994135843877, 'HP:0002795', 'Abnormal respiratory system physiology'),
(369043, 'HP:0033751', 'Elevated functional residual capacity', 'XPO:0101543', 'abnormal external gill', 0.41935483870967744, 6.780552239366747, 1.6862554345953, 'UPHENO:0004536', 'abnormal respiratory system'),
(369044, 'HP:0033751', 'Elevated functional residual capacity', 'XPO:0100004', 'abnormal cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(369045, 'HP:0033751', 'Elevated functional residual capacity', 'XPO:0101949', 'abnormal respiratory system morphology', 0.4864864864864865, 7.032762738978795, 1.8496875506903518, 'HP:0002795', 'Abnormal respiratory system physiology'),
(369046, 'HP:0033751', 'Elevated functional residual capacity', 'XPO:0130015', 'increased size of the respiratory system', 0.4090909090909091, 7.032762738978795, 1.6961837466234333, 'UPHENO:0002448', 'abnormality of respiratory system physiology'),
(369047, 'HP:0033751', 'Elevated functional residual capacity', 'XPO:0139850', 'abnormally necrotic respiratory system', 0.42857142857142855, 7.032762738978795, 1.7360994135843877, 'HP:0002795', 'Abnormal respiratory system physiology'),
(369048, 'HP:0033751', 'Elevated functional residual capacity', 'XPO:0128535', 'decreased size of the respiratory system', 0.4090909090909091, 7.032762738978795, 1.6961837466234333, 'HP:0002795', 'Abnormal respiratory system physiology'),
(369049, 'HP:0033751', 'Elevated functional residual capacity', 'XPO:0100317', 'abnormal respiratory system', 0.48148148148148145, 6.780552239366747, 1.8068509450070522, 'UPHENO:0004536', 'abnormal respiratory system'),
(369050, 'HP:0001611', 'Hypernasal speech', 'XPO:0101498', 'abnormal stage II oocyte', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(369051, 'HP:0001611', 'Hypernasal speech', 'XPO:0101480', 'abnormal stage V oocyte', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(369052, 'HP:0001611', 'Hypernasal speech', 'XPO:0100458', 'abnormal autopod', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(369053, 'HP:0001611', 'Hypernasal speech', 'XPO:0100638', 'abnormal polar body', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(369054, 'HP:0001611', 'Hypernasal speech', 'XPO:0100415', 'abnormal secretory epithelial cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(369055, 'HP:0001611', 'Hypernasal speech', 'XPO:0100242', 'abnormal right lymph heart', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(369056, 'HP:0001611', 'Hypernasal speech', 'XPO:0101010', 'abnormal dorsal marginal zone', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369057, 'HP:0001611', 'Hypernasal speech', 'XPO:0101297', 'abnormal barrier cell', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(369058, 'HP:0001611', 'Hypernasal speech', 'XPO:0100218', 'abnormal epithelial cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(369059, 'HP:0001611', 'Hypernasal speech', 'XPO:0141265', 'abnormal escape behavior', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(369060, 'HP:0001611', 'Hypernasal speech', 'XPO:0100070', 'abnormal anatomical system', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369061, 'HP:0001611', 'Hypernasal speech', 'XPO:0115505', 'dead whole organism', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369062, 'HP:0001611', 'Hypernasal speech', 'XPO:0101023', 'abnormal ultimobranchial body', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(369063, 'HP:0001611', 'Hypernasal speech', 'XPO:0101162', 'abnormal stromal cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(369064, 'HP:0001611', 'Hypernasal speech', 'XPO:0100588', 'abnormal unicellular gland', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369065, 'HP:0001611', 'Hypernasal speech', 'XPO:0115509', 'abnormally semi-viable whole organism', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369066, 'HP:0001611', 'Hypernasal speech', 'XPO:0141266', 'abnormal surface breathing', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(369067, 'HP:0001611', 'Hypernasal speech', 'XPO:0100707', 'abnormal central vegetal yolk mass', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369068, 'HP:0001611', 'Hypernasal speech', 'XPO:0100014', 'abnormal tissue', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369069, 'HP:0001611', 'Hypernasal speech', 'XPO:0101004', 'abnormal acid secreting cell', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(369070, 'HP:0001611', 'Hypernasal speech', 'XPO:0141718', 'abnormal posterior notochord', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(369071, 'HP:0001611', 'Hypernasal speech', 'XPO:0100954', 'abnormal neural progenitor cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(369072, 'HP:0001611', 'Hypernasal speech', 'XPO:0107326', 'abnormal regenerating pelvic girdle', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369073, 'HP:0001611', 'Hypernasal speech', 'XPO:0107259', 'abnormal animal-vegetal axis', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369074, 'HP:0001611', 'Hypernasal speech', 'XPO:0101072', 'abnormal mitochondrial cloud', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(369075, 'HP:0001611', 'Hypernasal speech', 'XPO:0126318', 'abnormally localised cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(369076, 'HP:0001611', 'Hypernasal speech', 'XPO:0100114', 'abnormal peripheral nervous system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(369077, 'HP:0001611', 'Hypernasal speech', 'XPO:0100540', 'abnormal left lymph heart', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(369078, 'HP:0001611', 'Hypernasal speech', 'XPO:0141784', 'abnormal cellular hormone metabolic process', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(369079, 'HP:0001611', 'Hypernasal speech', 'XPO:0107266', 'abnormal dorsal side', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369080, 'HP:0001611', 'Hypernasal speech', 'XPO:0131723', 'abnormal pathway-restricted SMAD protein phosphorylation', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(369081, 'HP:0001611', 'Hypernasal speech', 'XPO:0100727', 'abnormal odontogenic papilla', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(369082, 'HP:0001611', 'Hypernasal speech', 'XPO:0100484', 'abnormal cement gland primordium', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369083, 'HP:0001611', 'Hypernasal speech', 'XPO:0100501', 'abnormal urogenital system', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(369084, 'HP:0001611', 'Hypernasal speech', 'XPO:0141771', 'abnormal urea homeostasis', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(369085, 'HP:0001611', 'Hypernasal speech', 'XPO:0100133', 'abnormal solid compound organ', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369086, 'HP:0001611', 'Hypernasal speech', 'XPO:0100307', 'abnormal blastomere', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(369087, 'HP:0001611', 'Hypernasal speech', 'XPO:0100268', 'abnormal circulatory system', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369088, 'HP:0001611', 'Hypernasal speech', 'XPO:0101029', 'abnormal right spleen primordium', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(369089, 'HP:0001611', 'Hypernasal speech', 'XPO:0100715', 'abnormal ciliated cell', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(369090, 'HP:0001611', 'Hypernasal speech', 'XPO:0100486', 'abnormal oral evagination', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(369091, 'HP:0001611', 'Hypernasal speech', 'XPO:0131729', 'abnormal regulation of growth rate', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(369092, 'HP:0001611', 'Hypernasal speech', 'XPO:0128000', 'absent behavior', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(369093, 'HP:0001611', 'Hypernasal speech', 'XPO:0101092', 'abnormal dorso-lateral marginal zone', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369094, 'HP:0001611', 'Hypernasal speech', 'XPO:0100186', 'abnormal uveal tract', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369095, 'HP:0001611', 'Hypernasal speech', 'XPO:0101228', 'abnormal mesenchymal stem cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(369096, 'HP:0001611', 'Hypernasal speech', 'XPO:0101074', 'abnormal germinal vesicle', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(369097, 'HP:0001611', 'Hypernasal speech', 'XPO:0101302', 'abnormal subcortical cytoplasm', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(369098, 'HP:0001611', 'Hypernasal speech', 'XPO:0100640', 'abnormal notochordal sheath', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(369099, 'HP:0001611', 'Hypernasal speech', 'XPO:0100031', 'abnormal central nervous system', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(369100, 'HP:0001611', 'Hypernasal speech', 'XPO:0131469', 'abnormal heart process', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(369101, 'HP:0001611', 'Hypernasal speech', 'XPO:0100372', 'abnormal hematological system', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(369102, 'HP:0001611', 'Hypernasal speech', 'XPO:0107273', 'abnormal basal region', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369103, 'HP:0001611', 'Hypernasal speech', 'XPO:0100026', 'abnormal germ cell', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(369104, 'HP:0001611', 'Hypernasal speech', 'XPO:0101263', 'abnormal blastocoel floor', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369105, 'HP:0001611', 'Hypernasal speech', 'XPO:0100802', 'abnormal exocrine cell', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(369106, 'HP:0001611', 'Hypernasal speech', 'XPO:0107288', 'abnormal larval alimentary system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(369107, 'HP:0001611', 'Hypernasal speech', 'XPO:0100722', 'abnormal barbel', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369108, 'HP:0001611', 'Hypernasal speech', 'XPO:0100976', 'abnormal multiciliated cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(369109, 'HP:0001611', 'Hypernasal speech', 'XPO:0101389', 'abnormal wedge region', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(369110, 'HP:0001611', 'Hypernasal speech', 'XPO:0101976', 'abnormal portion of organism substance morphology', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369111, 'HP:0001611', 'Hypernasal speech', 'XPO:0100423', 'abnormal process', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369112, 'HP:0001611', 'Hypernasal speech', 'XPO:0101083', 'abnormal T cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(369113, 'HP:0001611', 'Hypernasal speech', 'XPO:0101212', 'abnormal glomeral mesenchyme', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(369114, 'HP:0001611', 'Hypernasal speech', 'XPO:0100858', 'abnormal presumptive midbrain-hindbrain boundary', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(369115, 'HP:0001611', 'Hypernasal speech', 'XPO:0100482', 'abnormal Mullerian duct', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(369116, 'HP:0001611', 'Hypernasal speech', 'XPO:0101237', 'abnormal mucus secreting cell', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(369117, 'HP:0001611', 'Hypernasal speech', 'XPO:0100781', 'abnormal presumptive ectoderm', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369118, 'HP:0001611', 'Hypernasal speech', 'XPO:0107272', 'abnormal axial region', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369119, 'HP:0001611', 'Hypernasal speech', 'XPO:0100816', 'abnormal blastocoel anlage', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369120, 'HP:0001611', 'Hypernasal speech', 'XPO:0107278', 'abnormal medial region', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369121, 'HP:0001611', 'Hypernasal speech', 'XPO:0101057', 'abnormal vegetal pole', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369122, 'HP:0001611', 'Hypernasal speech', 'XPO:0100084', 'abnormal anatomical group', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369123, 'HP:0001611', 'Hypernasal speech', 'XPO:0100852', 'abnormal interdigital region', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(369124, 'HP:0001611', 'Hypernasal speech', 'XPO:0100002', 'abnormal head', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(369125, 'HP:0001611', 'Hypernasal speech', 'XPO:0100741', 'abnormal blastopore', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369126, 'HP:0001611', 'Hypernasal speech', 'XPO:0101577', 'abnormal notochordal epithelium', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369127, 'HP:0001611', 'Hypernasal speech', 'XPO:0100991', 'abnormal iliac process primordium', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369128, 'HP:0001611', 'Hypernasal speech', 'XPO:0100261', 'abnormal multilaminar epithelium', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369129, 'HP:0001611', 'Hypernasal speech', 'XPO:0100339', 'abnormal circumblastoporal collar', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369130, 'HP:0001611', 'Hypernasal speech', 'XPO:0100653', 'abnormal myoblast', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(369131, 'HP:0001611', 'Hypernasal speech', 'XPO:0101406', 'abnormal cleavage furrow', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369132, 'HP:0001611', 'Hypernasal speech', 'XPO:0100557', 'abnormal prime meridian', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369133, 'HP:0001611', 'Hypernasal speech', 'XPO:0101409', 'abnormal perivitelline space', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(369134, 'HP:0001611', 'Hypernasal speech', 'XPO:0101451', 'abnormal dorsal lymph space', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(369135, 'HP:0001611', 'Hypernasal speech', 'XPO:0141781', 'abnormal secondary metabolic process', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(369136, 'HP:0001611', 'Hypernasal speech', 'XPO:0107269', 'abnormal right side', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369137, 'HP:0001611', 'Hypernasal speech', 'XPO:0100069', 'abnormal urinary system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(369138, 'HP:0001611', 'Hypernasal speech', 'XPO:0101107', 'abnormal erythroid cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(369139, 'HP:0001611', 'Hypernasal speech', 'XPO:0141714', 'abnormal anterior notochord', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(369140, 'HP:0001611', 'Hypernasal speech', 'XPO:0115512', 'abnormally semi-erect whole organism', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369141, 'HP:0001611', 'Hypernasal speech', 'XPO:0131730', 'abnormal regulation of protein folding', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(369142, 'HP:0001611', 'Hypernasal speech', 'XPO:0101078', 'abnormal mucous gland', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369143, 'HP:0001611', 'Hypernasal speech', 'XPO:0100762', 'abnormal intersomitic region', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369144, 'HP:0001611', 'Hypernasal speech', 'XPO:0100025', 'abnormal oocyte', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(369145, 'HP:0001611', 'Hypernasal speech', 'XPO:0100974', 'abnormal cardiac mesoderm', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369146, 'HP:0001611', 'Hypernasal speech', 'XPO:0101638', 'abnormal anatomical structure morphology', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369147, 'HP:0001611', 'Hypernasal speech', 'XPO:0100612', 'abnormal unilaminar epithelium', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369148, 'HP:0001611', 'Hypernasal speech', 'XPO:0101560', 'abnormal compound organ component', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369149, 'HP:0001611', 'Hypernasal speech', 'XPO:0100273', 'abnormal visual system', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(369150, 'HP:0001611', 'Hypernasal speech', 'XPO:0100521', 'abnormal animal blastomere', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(369151, 'HP:0001611', 'Hypernasal speech', 'XPO:0100293', 'abnormal duct', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369152, 'HP:0001611', 'Hypernasal speech', 'XPO:0141499', 'abnormal tadpole', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369153, 'HP:0001611', 'Hypernasal speech', 'XPO:0101368', 'abnormal regenerating eye', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369154, 'HP:0001611', 'Hypernasal speech', 'XPO:0101535', 'abnormal absorptive cell', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(369155, 'HP:0001611', 'Hypernasal speech', 'XPO:0100969', 'abnormal disaggregated/reaggregated ectoderm treated with activin', 0.5294117647058824, 1.706362323152461, 0.9504568842024205, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369156, 'HP:0001611', 'Hypernasal speech', 'XPO:0101468', 'abnormal stage I oocyte', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(369157, 'HP:0001611', 'Hypernasal speech', 'XPO:0141775', 'abnormal nitrogen compound metabolic process', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(369158, 'HP:0001611', 'Hypernasal speech', 'XPO:0115508', 'abnormally peramorphic growth of whole organism', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369159, 'HP:0001611', 'Hypernasal speech', 'XPO:0100255', 'abnormal pelvic appendage', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369160, 'HP:0001611', 'Hypernasal speech', 'XPO:0100796', 'abnormal pseudoblastema', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369161, 'HP:0001611', 'Hypernasal speech', 'XPO:0101040', 'abnormal axial mesoderm', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369162, 'HP:0001611', 'Hypernasal speech', 'XPO:0141315', 'abnormal anatomical region', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369163, 'HP:0001611', 'Hypernasal speech', 'XPO:0116494', 'absent biological process', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(369164, 'HP:0001611', 'Hypernasal speech', 'XPO:0142052', 'abnormal nasal region', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(369165, 'HP:0001611', 'Hypernasal speech', 'XPO:0100887', 'abnormal right-dorsal blastomere', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(369166, 'HP:0001611', 'Hypernasal speech', 'XPO:0100108', 'abnormal cell part', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(369167, 'HP:0001611', 'Hypernasal speech', 'XPO:0107263', 'abnormal anatomical side', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369168, 'HP:0001611', 'Hypernasal speech', 'XPO:0101519', 'abnormal hypobranchial placode', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369169, 'HP:0001611', 'Hypernasal speech', 'XPO:0100196', 'abnormal neuron', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(369170, 'HP:0001611', 'Hypernasal speech', 'XPO:0101589', 'abnormal blastocoel roof', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369171, 'HP:0001611', 'Hypernasal speech', 'XPO:0100754', 'abnormal electrically active cell', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(369172, 'HP:0001611', 'Hypernasal speech', 'XPO:0101096', 'abnormal tendon', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(369173, 'HP:0001611', 'Hypernasal speech', 'XPO:0141792', 'abnormal small molecule metabolic process', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(369174, 'HP:0001611', 'Hypernasal speech', 'XPO:0100377', 'abnormal connective tissue', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(369175, 'HP:0001611', 'Hypernasal speech', 'XPO:0100228', 'abnormal skeletal subdivision', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(369176, 'HP:0001611', 'Hypernasal speech', 'XPO:0107258', 'abnormal anatomical axis', 0.5294117647058824, 1.706362323152461, 0.9504568842024205, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369177, 'HP:0001611', 'Hypernasal speech', 'XPO:0100667', 'abnormal vegetal yolk mass', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369178, 'HP:0001611', 'Hypernasal speech', 'XPO:0100734', 'abnormal lateral line system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(369179, 'HP:0001611', 'Hypernasal speech', 'XPO:0101264', 'abnormal mitotic spindle', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(369180, 'HP:0001611', 'Hypernasal speech', 'XPO:0101490', 'abnormal ectodermal cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(369181, 'HP:0001611', 'Hypernasal speech', 'XPO:0100059', 'abnormal regenerating tail', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369182, 'HP:0001611', 'Hypernasal speech', 'XPO:0100913', 'abnormal Brachets cleft', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369183, 'HP:0001611', 'Hypernasal speech', 'XPO:0100282', 'abnormal pelvic girdle primordium', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369184, 'HP:0001611', 'Hypernasal speech', 'XPO:0100626', 'abnormal primordial germ cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(369185, 'HP:0001611', 'Hypernasal speech', 'XPO:0101402', 'abnormal oropharyngeal papilla', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(369186, 'HP:0001611', 'Hypernasal speech', 'XPO:0100509', 'abnormal germ plasm', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(369187, 'HP:0001611', 'Hypernasal speech', 'XPO:0100176', 'abnormal stage VI oocyte', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(369188, 'HP:0001611', 'Hypernasal speech', 'XPO:0100175', 'abnormal migrating neuroblast', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(369189, 'HP:0001611', 'Hypernasal speech', 'XPO:0141783', 'abnormal collagen metabolic process', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(369190, 'HP:0001611', 'Hypernasal speech', 'XPO:0100688', 'abnormal adipose tissue', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(369191, 'HP:0001611', 'Hypernasal speech', 'XPO:0101450', 'abnormal myeloid cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(369192, 'HP:0001611', 'Hypernasal speech', 'XPO:0101141', 'abnormal Keller explant', 0.5294117647058824, 1.706362323152461, 0.9504568842024205, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369193, 'HP:0001611', 'Hypernasal speech', 'XPO:0100156', 'abnormal foregut', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(369194, 'HP:0001611', 'Hypernasal speech', 'XPO:0101501', 'abnormal parabrachial area', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(369195, 'HP:0001611', 'Hypernasal speech', 'XPO:0100203', 'abnormal endocrine cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(369196, 'HP:0001611', 'Hypernasal speech', 'XPO:0107267', 'abnormal ventral side', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369197, 'HP:0001611', 'Hypernasal speech', 'XPO:0100854', 'abnormal spiracle', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369198, 'HP:0001611', 'Hypernasal speech', 'XPO:0100231', 'abnormal compound organ', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369199, 'HP:0001611', 'Hypernasal speech', 'XPO:0100060', 'abnormal regenerating tissue', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369200, 'HP:0001611', 'Hypernasal speech', 'XPO:0142056', 'abnormal main body axis', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369201, 'HP:0001611', 'Hypernasal speech', 'XPO:0131677', 'abnormal actin filament', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(369202, 'HP:0001611', 'Hypernasal speech', 'XPO:0100256', 'abnormal paired appendage', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369203, 'HP:0001611', 'Hypernasal speech', 'XPO:0100742', 'abnormal musculoskeletal system', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369204, 'HP:0001611', 'Hypernasal speech', 'XPO:0101403', 'abnormal basal lamina', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369205, 'HP:0001611', 'Hypernasal speech', 'XPO:0131745', 'abnormal axis elongation', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(369206, 'HP:0001611', 'Hypernasal speech', 'XPO:0101543', 'abnormal external gill', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(369207, 'HP:0001611', 'Hypernasal speech', 'XPO:0107339', 'abnormal yolk platelet', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(369208, 'HP:0001611', 'Hypernasal speech', 'XPO:0141715', 'abnormal septum', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369209, 'HP:0001611', 'Hypernasal speech', 'XPO:0100422', 'abnormal notochord', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(369210, 'HP:0001611', 'Hypernasal speech', 'XPO:0100515', 'abnormal somatic stem cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(369211, 'HP:0001611', 'Hypernasal speech', 'XPO:0100791', 'abnormal multiciliated cell precursor', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(369212, 'HP:0001611', 'Hypernasal speech', 'XPO:0100784', 'abnormal left blastomere', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(369213, 'HP:0001611', 'Hypernasal speech', 'XPO:0141860', 'abnormal malate-aspartate shuttle', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(369214, 'HP:0001611', 'Hypernasal speech', 'XPO:0100296', 'abnormal tail region', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369215, 'HP:0001611', 'Hypernasal speech', 'XPO:0100429', 'abnormal spermatid', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(369216, 'HP:0001611', 'Hypernasal speech', 'XPO:0100786', 'abnormal presumptive axial mesoderm', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369217, 'HP:0001611', 'Hypernasal speech', 'XPO:0100610', 'abnormal appendage', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369218, 'HP:0001611', 'Hypernasal speech', 'XPO:0100894', 'abnormal nucleus', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(369219, 'HP:0001611', 'Hypernasal speech', 'XPO:0142054', 'abnormal digestive tract', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(369220, 'HP:0001611', 'Hypernasal speech', 'XPO:0101326', 'abnormal cementoblast', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(369221, 'HP:0001611', 'Hypernasal speech', 'XPO:0131666', 'abnormal adherens junction', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(369222, 'HP:0001611', 'Hypernasal speech', 'XPO:0141782', 'abnormal methylation', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(369223, 'HP:0001611', 'Hypernasal speech', 'XPO:0100860', 'abnormal parathyroid', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(369224, 'HP:0001611', 'Hypernasal speech', 'XPO:0100376', 'abnormal animal pole', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369225, 'HP:0001611', 'Hypernasal speech', 'XPO:0101448', 'abnormal myelin accumulating cell', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(369226, 'HP:0001611', 'Hypernasal speech', 'XPO:0100135', 'abnormal surface structure', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369227, 'HP:0001611', 'Hypernasal speech', 'XPO:0100403', 'abnormal forelimb', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(369228, 'HP:0001611', 'Hypernasal speech', 'XPO:0100511', 'abnormal stylopod', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(369229, 'HP:0001611', 'Hypernasal speech', 'XPO:0141745', 'abnormal creatinine homeostasis', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(369230, 'HP:0001611', 'Hypernasal speech', 'XPO:0100827', 'abnormal atypical epithelium', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369231, 'HP:0001611', 'Hypernasal speech', 'XPO:0100691', 'abnormal keratin accumulating cell', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(369232, 'HP:0001611', 'Hypernasal speech', 'XPO:0100392', 'abnormal cilium', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(369233, 'HP:0001611', 'Hypernasal speech', 'XPO:0107270', 'abnormal proximal-distal axis', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369234, 'HP:0001611', 'Hypernasal speech', 'XPO:0107276', 'abnormal dorsal region', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369235, 'HP:0001611', 'Hypernasal speech', 'XPO:0100999', 'abnormal serous membrane', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369236, 'HP:0001611', 'Hypernasal speech', 'XPO:0100665', 'abnormal egg jelly', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369237, 'HP:0001611', 'Hypernasal speech', 'XPO:0141778', 'abnormal biosynthetic process', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(369238, 'HP:0001611', 'Hypernasal speech', 'XPO:0133403', 'abnormal developmental process', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(369239, 'HP:0001611', 'Hypernasal speech', 'XPO:0107285', 'abnormal flexural organ', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(369240, 'HP:0001611', 'Hypernasal speech', 'XPO:0101311', 'abnormal bottle cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(369241, 'HP:0001611', 'Hypernasal speech', 'XPO:0100726', 'abnormal tail', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369242, 'HP:0001611', 'Hypernasal speech', 'XPO:0101333', 'abnormal barrier epithelial cell', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(369243, 'HP:0001611', 'Hypernasal speech', 'XPO:0141794', 'abnormal prosthetic group metabolic process', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(369244, 'HP:0001611', 'Hypernasal speech', 'XPO:0142057', 'abnormal desmosome', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(369245, 'HP:0001611', 'Hypernasal speech', 'XPO:0101533', 'abnormal simple cuboidal epithelium', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369246, 'HP:0001611', 'Hypernasal speech', 'XPO:0115391', 'abnormally undifferentiated alimentary system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(369247, 'HP:0001611', 'Hypernasal speech', 'XPO:0101573', 'abnormal peripheral vegetal yolk mass', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369248, 'HP:0001611', 'Hypernasal speech', 'XPO:0100104', 'abnormal embryonic structure', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369249, 'HP:0001611', 'Hypernasal speech', 'XPO:0101553', 'abnormal dental epithelium', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369250, 'HP:0001611', 'Hypernasal speech', 'XPO:0100285', 'abnormal progenitor cell', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(369251, 'HP:0001611', 'Hypernasal speech', 'XPO:0141263', 'abnormal visually guided collision avoidance behavior', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(369252, 'HP:0001611', 'Hypernasal speech', 'XPO:0100265', 'abnormal sensory epithelial cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(369253, 'HP:0001611', 'Hypernasal speech', 'XPO:0100172', 'abnormal stem cell', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(369254, 'HP:0001611', 'Hypernasal speech', 'XPO:0141796', 'abnormal demethylation', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(369255, 'HP:0001611', 'Hypernasal speech', 'XPO:0101461', 'abnormal sperm entry point', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(369256, 'HP:0001611', 'Hypernasal speech', 'XPO:0100062', 'abnormal anatomical space', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369257, 'HP:0001611', 'Hypernasal speech', 'XPO:0131667', 'abnormal actin cytoskeleton', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(369258, 'HP:0001611', 'Hypernasal speech', 'XPO:0107312', 'abnormal filopodium', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(369259, 'HP:0001611', 'Hypernasal speech', 'XPO:0100267', 'abnormal wound epidermis', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369260, 'HP:0001611', 'Hypernasal speech', 'XPO:0131669', 'abnormal Roux spot', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(369261, 'HP:0001611', 'Hypernasal speech', 'XPO:0141738', 'abnormal carbon dioxide homeostasis', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(369262, 'HP:0001611', 'Hypernasal speech', 'XPO:0100917', 'abnormal stage III oocyte', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(369263, 'HP:0001611', 'Hypernasal speech', 'XPO:0101224', 'abnormal dorsal involuting marginal zone', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369264, 'HP:0001611', 'Hypernasal speech', 'XPO:0100028', 'abnormal anatomical cluster', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369265, 'HP:0001611', 'Hypernasal speech', 'XPO:0141267', 'abnormal resting posture', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(369266, 'HP:0001611', 'Hypernasal speech', 'XPO:0100701', 'abnormal microglial cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(369267, 'HP:0001611', 'Hypernasal speech', 'XPO:0100503', 'abnormal blastomere D2', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(369268, 'HP:0001611', 'Hypernasal speech', 'XPO:0100337', 'abnormal zygote', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(369269, 'HP:0001611', 'Hypernasal speech', 'XPO:0100899', 'abnormal secondary spermatogonium', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(369270, 'HP:0001611', 'Hypernasal speech', 'XPO:0101061', 'abnormal plasma membrane', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(369271, 'HP:0001611', 'Hypernasal speech', 'XPO:0100867', 'abnormal apical mesenchyme', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369272, 'HP:0001611', 'Hypernasal speech', 'XPO:0100553', 'abnormal laryngeal muscle primordium', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369273, 'HP:0001611', 'Hypernasal speech', 'XPO:0101113', 'abnormal stage IV oocyte', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(369274, 'HP:0001611', 'Hypernasal speech', 'XPO:0107311', 'abnormal apical junction complex', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(369275, 'HP:0001611', 'Hypernasal speech', 'XPO:0100864', 'abnormal dorsolateral ascending neuron', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(369276, 'HP:0001611', 'Hypernasal speech', 'XPO:0100581', 'abnormal immune system', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(369277, 'HP:0001611', 'Hypernasal speech', 'XPO:0141600', 'absent metamorphosis', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(369278, 'HP:0001611', 'Hypernasal speech', 'XPO:0101174', 'abnormal articular system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(369279, 'HP:0001611', 'Hypernasal speech', 'XPO:0141777', 'abnormal catabolic process', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(369280, 'HP:0001611', 'Hypernasal speech', 'XPO:0100402', 'abnormal zeugopod', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(369281, 'HP:0001611', 'Hypernasal speech', 'XPO:0141271', 'increased surface breathing', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(369282, 'HP:0001611', 'Hypernasal speech', 'XPO:0100674', 'abnormal secondary oogonium', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(369283, 'HP:0001611', 'Hypernasal speech', 'XPO:0101149', 'abnormal amputated limb', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369284, 'HP:0001611', 'Hypernasal speech', 'XPO:0100735', 'abnormal hindgut', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(369285, 'HP:0001611', 'Hypernasal speech', 'XPO:0107284', 'abnormal migrating myoblast', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(369286, 'HP:0001611', 'Hypernasal speech', 'XPO:0100799', 'abnormal genital ridge', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(369287, 'HP:0001611', 'Hypernasal speech', 'XPO:0107271', 'abnormal apical region', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369288, 'HP:0001611', 'Hypernasal speech', 'XPO:0100427', 'abnormal olfactory system', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(369289, 'HP:0001611', 'Hypernasal speech', 'XPO:0100120', 'abnormal genital system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(369290, 'HP:0001611', 'Hypernasal speech', 'XPO:0116434', 'abnormal biological process', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(369291, 'HP:0001611', 'Hypernasal speech', 'XPO:0131725', 'abnormal phosphorylation of RNA polymerase II C-terminal domain', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(369292, 'HP:0001611', 'Hypernasal speech', 'XPO:0100989', 'abnormal right blastomere', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(369293, 'HP:0001611', 'Hypernasal speech', 'XPO:0100295', 'abnormal extracellular matrix', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369294, 'HP:0001611', 'Hypernasal speech', 'XPO:0100417', 'abnormal dense regular connective tissue', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(369295, 'HP:0001611', 'Hypernasal speech', 'XPO:0100100', 'abnormal muscle', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(369296, 'HP:0001611', 'Hypernasal speech', 'XPO:0101109', 'abnormal egg cell-free extract', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369297, 'HP:0001611', 'Hypernasal speech', 'XPO:0100003', 'abnormal organism subdivision', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369298, 'HP:0001611', 'Hypernasal speech', 'XPO:0101570', 'abnormal forelimb region', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369299, 'HP:0001611', 'Hypernasal speech', 'XPO:0141748', 'abnormal gas homeostasis', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(369300, 'HP:0001611', 'Hypernasal speech', 'XPO:0100890', 'abnormal pharyngeal cavity', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(369301, 'HP:0001611', 'Hypernasal speech', 'XPO:0100363', 'abnormal cardiovascular system', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369302, 'HP:0001611', 'Hypernasal speech', 'XPO:0100574', 'abnormal gastrula cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(369303, 'HP:0001611', 'Hypernasal speech', 'XPO:0100398', 'abnormal vegetal blastomere', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(369304, 'HP:0001611', 'Hypernasal speech', 'XPO:0100449', 'abnormal lymphocyte', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(369305, 'HP:0001611', 'Hypernasal speech', 'XPO:0100317', 'abnormal respiratory system', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(369306, 'HP:0001611', 'Hypernasal speech', 'XPO:0100842', 'abnormal left-dorsal blastomere', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(369307, 'HP:0001611', 'Hypernasal speech', 'XPO:0100546', 'abnormal whole organism', 0.5294117647058824, 1.706362323152461, 0.9504568842024205, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369308, 'HP:0001611', 'Hypernasal speech', 'XPO:0100547', 'abnormal blastomere V2', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(369309, 'HP:0001611', 'Hypernasal speech', 'XPO:0100481', 'abnormal anatomical line', 0.5625, 1.706362323152461, 0.9797085315405084, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369310, 'HP:0001611', 'Hypernasal speech', 'XPO:0100724', 'abnormal kinetochore', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(369311, 'HP:0001611', 'Hypernasal speech', 'XPO:0101500', 'abnormal endodermal cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(369312, 'HP:0001611', 'Hypernasal speech', 'XPO:0100728', 'abnormal cell condensation', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369313, 'HP:0001611', 'Hypernasal speech', 'XPO:0100258', 'abnormal organ part', 0.5294117647058824, 1.706362323152461, 0.9504568842024205, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369314, 'HP:0001611', 'Hypernasal speech', 'XPO:0141892', 'abnormal inositol metabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(369315, 'HP:0001611', 'Hypernasal speech', 'XPO:0100902', 'abnormal spermatocyte', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(369316, 'HP:0001611', 'Hypernasal speech', 'XPO:0100916', 'abnormal principal cavity', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(369317, 'HP:0001611', 'Hypernasal speech', 'XPO:0100533', 'abnormal melanoblast', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(369318, 'HP:0001611', 'Hypernasal speech', 'XPO:0100023', 'abnormal mesenchyme', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369319, 'HP:0001611', 'Hypernasal speech', 'XPO:0100800', 'abnormal ventral marginal zone', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369320, 'HP:0001611', 'Hypernasal speech', 'XPO:0115574', 'abnormal variability of size of hindlimb', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(369321, 'HP:0001611', 'Hypernasal speech', 'XPO:0100585', 'abnormal elastica externa', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(369322, 'HP:0001611', 'Hypernasal speech', 'XPO:0100093', 'abnormal simple squamous epithelium', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369323, 'HP:0001611', 'Hypernasal speech', 'XPO:0101378', 'abnormal blastomere D1', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(369324, 'HP:0001611', 'Hypernasal speech', 'XPO:0107253', 'abnormal enteric nervous system', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(369325, 'HP:0001611', 'Hypernasal speech', 'XPO:0141795', 'abnormal glycosylation', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(369326, 'HP:0001611', 'Hypernasal speech', 'XPO:0100378', 'abnormal perichondrium', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(369327, 'HP:0001611', 'Hypernasal speech', 'XPO:0100721', 'abnormal centromere', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(369328, 'HP:0001611', 'Hypernasal speech', 'XPO:0100187', 'abnormal regenerating limb', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369329, 'HP:0001611', 'Hypernasal speech', 'XPO:0100643', 'abnormal thoracic region', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369330, 'HP:0001611', 'Hypernasal speech', 'XPO:0115473', 'abnormally delayed phase of Mullerian duct', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(369331, 'HP:0001611', 'Hypernasal speech', 'XPO:0115362', 'abnormally decreased adhesivity of prechordal plate', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369332, 'HP:0001611', 'Hypernasal speech', 'XPO:0100393', 'abnormal involuting marginal zone', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369333, 'HP:0001611', 'Hypernasal speech', 'XPO:0101071', 'abnormal endoplasmic reticulum', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(369334, 'HP:0001611', 'Hypernasal speech', 'XPO:0107265', 'abnormal posterior side', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369335, 'HP:0001611', 'Hypernasal speech', 'XPO:0131685', 'abnormal cortical actin cytoskeleton', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(369336, 'HP:0001611', 'Hypernasal speech', 'XPO:0141743', 'abnormal chemical homeostasis within a tissue', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(369337, 'HP:0001611', 'Hypernasal speech', 'XPO:0100868', 'abnormal transporting epithelium', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369338, 'HP:0001611', 'Hypernasal speech', 'XPO:0100277', 'abnormal blastocoel', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369339, 'HP:0001611', 'Hypernasal speech', 'XPO:0100146', 'abnormal primary germ layer', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369340, 'HP:0001611', 'Hypernasal speech', 'XPO:0100249', 'abnormal avascular GAG-rich matrix', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369341, 'HP:0001611', 'Hypernasal speech', 'XPO:0141497', 'abnormal lymphoblast', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(369342, 'HP:0001611', 'Hypernasal speech', 'XPO:0100985', 'abnormal simple columnar epithelium', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369343, 'HP:0001611', 'Hypernasal speech', 'XPO:0100202', 'abnormal embryo', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369344, 'HP:0001611', 'Hypernasal speech', 'XPO:0100627', 'abnormal pharyngeal region', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(369345, 'HP:0001611', 'Hypernasal speech', 'XPO:0101569', 'abnormal activin-induced ectoderm', 0.5294117647058824, 1.706362323152461, 0.9504568842024205, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369346, 'HP:0001611', 'Hypernasal speech', 'XPO:0101241', 'abnormal nucleate erythrocyte', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(369347, 'HP:0001611', 'Hypernasal speech', 'XPO:0100251', 'abnormal proteinaceous extracellular matrix', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369348, 'HP:0001611', 'Hypernasal speech', 'XPO:0100332', 'abnormal germinal granule', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(369349, 'HP:0001611', 'Hypernasal speech', 'XPO:0142051', 'abnormal cerebrospinal fluid', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(369350, 'HP:0001611', 'Hypernasal speech', 'XPO:0100807', 'abnormal matrix-based tissue', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369351, 'HP:0001611', 'Hypernasal speech', 'XPO:0100846', 'abnormal hindlimb', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(369352, 'HP:0001611', 'Hypernasal speech', 'XPO:0107268', 'abnormal left side', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369353, 'HP:0001611', 'Hypernasal speech', 'XPO:0115566', 'abnormal variability of size of forelimb', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(369354, 'HP:0001611', 'Hypernasal speech', 'XPO:0100823', 'abnormal blood', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(369355, 'HP:0001611', 'Hypernasal speech', 'XPO:0100162', 'abnormal presumptive rhombomere', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369356, 'HP:0001611', 'Hypernasal speech', 'XPO:0100573', 'abnormal extraembryonic structure', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369357, 'HP:0001611', 'Hypernasal speech', 'XPO:0100915', 'abnormal dermal system', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369358, 'HP:0001611', 'Hypernasal speech', 'XPO:0100587', 'abnormal vestibuloauditory system', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(369359, 'HP:0001611', 'Hypernasal speech', 'XPO:0101503', 'abnormal organ cortex', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369360, 'HP:0001611', 'Hypernasal speech', 'XPO:0101349', 'abnormal trunk region', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369361, 'HP:0001611', 'Hypernasal speech', 'XPO:0100383', 'abnormal amputated fin', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369362, 'HP:0001611', 'Hypernasal speech', 'XPO:0101460', 'abnormal fibrocellular pad', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369363, 'HP:0001611', 'Hypernasal speech', 'XPO:0101200', 'abnormal joint region', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369364, 'HP:0001611', 'Hypernasal speech', 'XPO:0100888', 'abnormal microtubule', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(369365, 'HP:0001611', 'Hypernasal speech', 'XPO:0101424', 'abnormal coelomic epithelium', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369366, 'HP:0001611', 'Hypernasal speech', 'XPO:0100862', 'abnormal blastomere V1', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(369367, 'HP:0001611', 'Hypernasal speech', 'XPO:0100205', 'abnormal limb segment', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(369368, 'HP:0001611', 'Hypernasal speech', 'XPO:0100912', 'abnormal trabecula', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369369, 'HP:0001611', 'Hypernasal speech', 'XPO:0100164', 'abnormal neural nucleus', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(369370, 'HP:0001611', 'Hypernasal speech', 'XPO:0101110', 'abnormal cell-free extract', 0.5294117647058824, 1.706362323152461, 0.9504568842024205, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369371, 'HP:0001611', 'Hypernasal speech', 'XPO:0100032', 'abnormal nervous system', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(369372, 'HP:0001611', 'Hypernasal speech', 'XPO:0100465', 'abnormal skeletal system', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(369373, 'HP:0001611', 'Hypernasal speech', 'XPO:0100605', 'abnormal prechordal plate', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369374, 'HP:0001611', 'Hypernasal speech', 'XPO:0100433', 'abnormal pectoral appendage', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369375, 'HP:0001611', 'Hypernasal speech', 'XPO:0100437', 'abnormal proepicardium', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(369376, 'HP:0001611', 'Hypernasal speech', 'XPO:0101098', 'abnormal mineralized extracellular matrix', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369377, 'HP:0001611', 'Hypernasal speech', 'XPO:0100468', 'abnormal muscular system', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369378, 'HP:0001611', 'Hypernasal speech', 'XPO:0101157', 'abnormal female organism', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369379, 'HP:0001611', 'Hypernasal speech', 'XPO:0101405', 'abnormal ring structure', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(369380, 'HP:0001611', 'Hypernasal speech', 'XPO:0100907', 'abnormal cytoplasm', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(369381, 'HP:0001611', 'Hypernasal speech', 'XPO:0101269', 'abnormal mesodermal cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(369382, 'HP:0001611', 'Hypernasal speech', 'XPO:0101713', 'abnormal anatomical entity in vitro morphology', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369383, 'HP:0001611', 'Hypernasal speech', 'XPO:0101513', 'abnormal basal body', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(369384, 'HP:0001611', 'Hypernasal speech', 'XPO:0100702', 'abnormal glial cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(369385, 'HP:0001611', 'Hypernasal speech', 'XPO:0100152', 'abnormal alimentary system', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(369386, 'HP:0001611', 'Hypernasal speech', 'XPO:0100956', 'abnormal centrosome', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(369387, 'HP:0001611', 'Hypernasal speech', 'XPO:0101240', 'abnormal ciliated non-epidermal cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(369388, 'HP:0001611', 'Hypernasal speech', 'XPO:0141797', 'abnormal hydrogen metabolic process', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(369389, 'HP:0001611', 'Hypernasal speech', 'XPO:0101168', 'abnormal circulating cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(369390, 'HP:0001611', 'Hypernasal speech', 'XPO:0100004', 'abnormal cell', 0.55, 1.8210412618256888, 1.0007860380741376, 'HP:0000118', 'Phenotypic abnormality'),
(369391, 'HP:0001611', 'Hypernasal speech', 'XPO:0101133', 'abnormal motor neuron', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(369392, 'HP:0001611', 'Hypernasal speech', 'XPO:0101467', 'abnormal alkali secreting cell', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(369393, 'HP:0001611', 'Hypernasal speech', 'XPO:0100386', 'abnormal limb', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(369394, 'HP:0001611', 'Hypernasal speech', 'XPO:0101099', 'abnormal ventro-lateral marginal zone', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369395, 'HP:0001611', 'Hypernasal speech', 'XPO:0100616', 'abnormal ventral blood island', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(369396, 'HP:0001611', 'Hypernasal speech', 'XPO:0101221', 'abnormal larval immune system', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(369397, 'HP:0001611', 'Hypernasal speech', 'XPO:0101373', 'abnormal oxygen accumulating cell', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(369398, 'HP:0001611', 'Hypernasal speech', 'XPO:0100394', 'abnormal marginal zone', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369399, 'HP:0001611', 'Hypernasal speech', 'XPO:0100493', 'abnormal liver and biliary system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(369400, 'HP:0001611', 'Hypernasal speech', 'XPO:0100687', 'abnormal periotic region', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(369401, 'HP:0001611', 'Hypernasal speech', 'XPO:0127101', 'abnormally localised portion of organism substance', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369402, 'HP:0001611', 'Hypernasal speech', 'XPO:0141798', 'abnormal lipid metabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(369403, 'HP:0001611', 'Hypernasal speech', 'XPO:0100274', 'abnormal sensory system', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(369404, 'HP:0001611', 'Hypernasal speech', 'XPO:0100750', 'abnormal regenerating fin', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369405, 'HP:0001611', 'Hypernasal speech', 'XPO:0100289', 'abnormal chondroblast', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(369406, 'HP:0001611', 'Hypernasal speech', 'XPO:0100531', 'abnormal proliferative region', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369407, 'HP:0001611', 'Hypernasal speech', 'XPO:0126624', 'abnormally localised anatomical line', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369408, 'HP:0001611', 'Hypernasal speech', 'XPO:0100537', 'abnormal medium cavity', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(369409, 'HP:0001611', 'Hypernasal speech', 'XPO:0133388', 'absent insulin receptor signaling pathway', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(369410, 'HP:0001611', 'Hypernasal speech', 'XPO:0101472', 'abnormal zygote cortex', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(369411, 'HP:0001611', 'Hypernasal speech', 'XPO:0124719', 'absent anatomical structure', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369412, 'HP:0001611', 'Hypernasal speech', 'XPO:0101435', 'abnormal paracrine cell', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(369413, 'HP:0001611', 'Hypernasal speech', 'XPO:0107264', 'abnormal anterior side', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369414, 'HP:0001611', 'Hypernasal speech', 'XPO:0141904', 'abnormal glucosamine metabolic process', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(369415, 'HP:0001611', 'Hypernasal speech', 'XPO:0100551', 'abnormal oocyte cortex', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(369416, 'HP:0001611', 'Hypernasal speech', 'XPO:0115758', 'abnormally decreased mobility of melanoblast', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(369417, 'HP:0001611', 'Hypernasal speech', 'XPO:0100872', 'abnormal neuroendocrine cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(369418, 'HP:0001611', 'Hypernasal speech', 'XPO:0101220', 'abnormal centriole', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(369419, 'HP:0001611', 'Hypernasal speech', 'XPO:0100935', 'abnormal skeleton', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(369420, 'HP:0001611', 'Hypernasal speech', 'XPO:0100856', 'abnormal simple organ', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369421, 'HP:0001611', 'Hypernasal speech', 'XPO:0100225', 'abnormal endocrine system', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(369422, 'HP:0001611', 'Hypernasal speech', 'XPO:0100103', 'abnormal trunk', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369423, 'HP:0001611', 'Hypernasal speech', 'XPO:00000000', 'Xenopus phenotype', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(369424, 'HP:0001611', 'Hypernasal speech', 'XPO:0141264', 'abnormal schooling behavior', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(369425, 'HP:0001611', 'Hypernasal speech', 'XPO:0100745', 'abnormal anterior lymph sac', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(369426, 'HP:0001611', 'Hypernasal speech', 'XPO:0100384', 'abnormal amputated tissue', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369427, 'HP:0001611', 'Hypernasal speech', 'XPO:0100704', 'abnormal Merkel cell', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(369428, 'HP:0001611', 'Hypernasal speech', 'XPO:0100232', 'abnormal lymphatic system', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(369429, 'HP:0001611', 'Hypernasal speech', 'XPO:0100900', 'abnormal angioblast', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(369430, 'HP:0001611', 'Hypernasal speech', 'XPO:0141276', 'decreased surface breathing', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(369431, 'HP:0001611', 'Hypernasal speech', 'XPO:0100416', 'abnormal ligament', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(369432, 'HP:0001611', 'Hypernasal speech', 'XPO:0101347', 'abnormal hindlimb region', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369433, 'HP:0001611', 'Hypernasal speech', 'XPO:0101740', 'abnormal cell part morphology', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(369434, 'HP:0001611', 'Hypernasal speech', 'XPO:0125007', 'absent anatomical line', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369435, 'HP:0001611', 'Hypernasal speech', 'XPO:0116091', 'abnormally increased variability of size of cell in endoderm', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(369436, 'HP:0001611', 'Hypernasal speech', 'XPO:0100010', 'abnormal multicellular anatomical structure', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369437, 'HP:0001611', 'Hypernasal speech', 'XPO:0100477', 'abnormal pericyte', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(369438, 'HP:0001611', 'Hypernasal speech', 'XPO:0101463', 'abnormal right-ventral blastomere', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(369439, 'HP:0001611', 'Hypernasal speech', 'XPO:0141272', 'absent surface breathing', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(369440, 'HP:0001611', 'Hypernasal speech', 'XPO:0100239', 'abnormal acellular anatomical structure', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369441, 'HP:0001611', 'Hypernasal speech', 'XPO:0107262', 'abnormal left-right axis', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369442, 'HP:0001611', 'Hypernasal speech', 'XPO:0101132', 'abnormal apoptotic cell', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(369443, 'HP:0001611', 'Hypernasal speech', 'XPO:0101575', 'abnormal vitelline membrane', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(369444, 'HP:0001611', 'Hypernasal speech', 'XPO:0101187', 'abnormal dorsolateral commissural neuron', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(369445, 'HP:0001611', 'Hypernasal speech', 'XPO:0100642', 'abnormal gustatory system', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(369446, 'HP:0001611', 'Hypernasal speech', 'XPO:0141772', 'abnormal water homeostasis', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(369447, 'HP:0001611', 'Hypernasal speech', 'XPO:0101547', 'abnormal lampbrush chromosome', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(369448, 'HP:0001611', 'Hypernasal speech', 'XPO:0101283', 'abnormal left-ventral blastomere', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(369449, 'HP:0001611', 'Hypernasal speech', 'XPO:0141770', 'abnormal urate homeostasis', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(369450, 'HP:0001611', 'Hypernasal speech', 'XPO:0100009', 'abnormal multi-tissue structure', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369451, 'HP:0001611', 'Hypernasal speech', 'XPO:0141754', 'abnormal homeostatic process', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(369452, 'HP:0001611', 'Hypernasal speech', 'XPO:0102113', 'abnormal anatomical line morphology', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369453, 'HP:0001611', 'Hypernasal speech', 'XPO:0100192', 'abnormal epithelium', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369454, 'HP:0001611', 'Hypernasal speech', 'XPO:0141786', 'abnormal pigment metabolic process', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(369455, 'HP:0001611', 'Hypernasal speech', 'XPO:0107261', 'abnormal dorsal-ventral axis', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369456, 'HP:0001611', 'Hypernasal speech', 'XPO:0141907', 'abnormal putrescine metabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(369457, 'HP:0001611', 'Hypernasal speech', 'XPO:0100664', 'abnormal periocular region', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(369458, 'HP:0001611', 'Hypernasal speech', 'XPO:0126321', 'abnormally localised anatomical structure', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369459, 'HP:0001611', 'Hypernasal speech', 'XPO:0101366', 'abnormal morula cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(369460, 'HP:0001611', 'Hypernasal speech', 'XPO:0131675', 'abnormal spindle microtubule', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(369461, 'HP:0001611', 'Hypernasal speech', 'XPO:0100760', 'abnormal Stirnorgan', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(369462, 'HP:0001611', 'Hypernasal speech', 'XPO:0101396', 'abnormal apical epithelial cap', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369463, 'HP:0001611', 'Hypernasal speech', 'XPO:0100549', 'abnormal mitotic cell', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(369464, 'HP:0001611', 'Hypernasal speech', 'XPO:0100523', 'abnormal midgut', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(369465, 'HP:0001611', 'Hypernasal speech', 'XPO:0101136', 'abnormal ooplasm', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(369466, 'HP:0001611', 'Hypernasal speech', 'XPO:0141790', 'abnormal cellular metabolic process', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(369467, 'HP:0001611', 'Hypernasal speech', 'XPO:0100599', 'abnormal adult immune system', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(369468, 'HP:0001611', 'Hypernasal speech', 'XPO:0141791', 'abnormal primary metabolic process', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(369469, 'HP:0001611', 'Hypernasal speech', 'XPO:0100067', 'abnormal animal hemisphere', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369470, 'HP:0001611', 'Hypernasal speech', 'XPO:0101411', 'abnormal marginal zone (sensu neural)', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369471, 'HP:0001611', 'Hypernasal speech', 'XPO:0100158', 'abnormal neuromere', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(369472, 'HP:0001611', 'Hypernasal speech', 'XPO:0101176', 'abnormal non-ciliated epithelial cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(369473, 'HP:0001611', 'Hypernasal speech', 'XPO:0100151', 'abnormal primordium', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369474, 'HP:0001611', 'Hypernasal speech', 'XPO:0107260', 'abnormal anterior-posterior axis', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369475, 'HP:0001611', 'Hypernasal speech', 'XPO:0100006', 'abnormal anatomical structure', 0.5625, 1.706362323152461, 0.9797085315405084, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369476, 'HP:0001611', 'Hypernasal speech', 'XPO:0131687', 'abnormal astral microtubule', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(369477, 'HP:0001611', 'Hypernasal speech', 'XPO:0100081', 'abnormal anatomical entity in vitro', 0.5625, 1.706362323152461, 0.9797085315405084, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369478, 'HP:0001611', 'Hypernasal speech', 'XPO:0101587', 'abnormal hemangioblast', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(369479, 'HP:0001611', 'Hypernasal speech', 'XPO:0100843', 'abnormal fasciculated network of fibrils', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(369480, 'HP:0001611', 'Hypernasal speech', 'XPO:0100309', 'abnormal vegetal hemisphere', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369481, 'HP:0001611', 'Hypernasal speech', 'XPO:0101377', 'abnormal manicotto glandulare', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(369482, 'HP:0001611', 'Hypernasal speech', 'XPO:0131691', 'abnormal molecular function', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(369483, 'HP:0001611', 'Hypernasal speech', 'XPO:0100545', 'abnormal male organism', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369484, 'HP:0001611', 'Hypernasal speech', 'XPO:0101518', 'abnormal B cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(369485, 'HP:0001611', 'Hypernasal speech', 'XPO:0100344', 'abnormal portion of organism substance', 0.5625, 1.706362323152461, 0.9797085315405084, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369486, 'HP:0001611', 'Hypernasal speech', 'XPO:0100207', 'abnormal blastema', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369487, 'HP:0001611', 'Hypernasal speech', 'XPO:0141776', 'abnormal metabolic process', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(369488, 'HP:0001611', 'Hypernasal speech', 'XPO:0101497', 'abnormal ciliary axoneme', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(369489, 'HP:0001611', 'Hypernasal speech', 'XPO:0101362', 'abnormal vegetal cortex', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(369490, 'HP:0001611', 'Hypernasal speech', 'XPO:0100201', 'abnormal cavitated compound organ', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369491, 'HP:0001611', 'Hypernasal speech', 'XPO:0100308', 'abnormal early embryonic cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(369492, 'HP:0001611', 'Hypernasal speech', 'XPO:0141787', 'abnormal hormone metabolic process', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(369493, 'HP:0001611', 'Hypernasal speech', 'XPO:0100444', 'abnormal cement gland', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(369494, 'HP:0001611', 'Hypernasal speech', 'XPO:0141809', 'abnormal catalytic activity', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(369495, 'HP:0001611', 'Hypernasal speech', 'XPO:0100189', 'abnormal enteroendocrine cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(369496, 'HP:0001611', 'Hypernasal speech', 'XPO:0141841', 'abnormality of whole organism mass', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(369497, 'HP:0005765', 'Sacral meningocele', 'XPO:0128306', 'decreased size of the articular system', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(369498, 'HP:0005765', 'Sacral meningocele', 'XPO:0100927', 'abnormal sacral vertebra', 0.4098360655737705, 8.05344015541032, 1.816752660002781, 'UPHENO:0002813', 'abnormal vertebral column'),
(369499, 'HP:0005765', 'Sacral meningocele', 'XPO:0102272', 'abnormal notochordal sheath morphology', 0.46511627906976744, 4.638757693672553, 1.4688640910537754, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(369500, 'HP:0005765', 'Sacral meningocele', 'XPO:0101858', 'abnormal vertebral element morphology', 0.4642857142857143, 8.361863005979023, 1.9703536582274415, 'UPHENO:0076695', 'abnormal vertebral column morphology'),
(369501, 'HP:0005765', 'Sacral meningocele', 'XPO:0130060', 'increased size of the postcranial axial skeleton', 0.41818181818181815, 6.272837960958401, 1.6196255072310737, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(369502, 'HP:0005765', 'Sacral meningocele', 'XPO:0140559', 'abnormally necrotic articular system', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(369503, 'HP:0005765', 'Sacral meningocele', 'XPO:0102054', 'abnormal notochord morphology', 0.46511627906976744, 4.638757693672553, 1.4688640910537754, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(369504, 'HP:0005765', 'Sacral meningocele', 'XPO:0128352', 'decreased size of the skeletal system', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(369505, 'HP:0005765', 'Sacral meningocele', 'XPO:0128580', 'decreased size of the postcranial axial skeleton', 0.41818181818181815, 6.272837960958401, 1.6196255072310737, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(369506, 'HP:0005765', 'Sacral meningocele', 'XPO:0102514', 'abnormal perichondrial cell morphology', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(369507, 'HP:0005765', 'Sacral meningocele', 'XPO:0126787', 'abnormally localised vertebral centrum', 0.4098360655737705, 8.05344015541032, 1.816752660002781, 'UPHENO:0002813', 'abnormal vertebral column'),
(369508, 'HP:0005765', 'Sacral meningocele', 'XPO:0126886', 'abnormally localised vertebral column', 0.4807692307692308, 8.05344015541032, 1.9677007466997247, 'UPHENO:0002813', 'abnormal vertebral column'),
(369509, 'HP:0005765', 'Sacral meningocele', 'XPO:0140350', 'abnormally necrotic notochordal sheath', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(369510, 'HP:0005765', 'Sacral meningocele', 'XPO:0100693', 'abnormal vertebral centrum', 0.5, 8.05344015541032, 2.0066689008665977, 'UPHENO:0002813', 'abnormal vertebral column'),
(369511, 'HP:0005765', 'Sacral meningocele', 'XPO:0102217', 'abnormal elastica externa morphology', 0.4878048780487805, 4.638757693672553, 1.5042634845863214, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(369512, 'HP:0005765', 'Sacral meningocele', 'XPO:0102164', 'abnormal mandibular mesenchyme morphology', 0.40384615384615385, 6.211345574613551, 1.5838017617482976, 'UPHENO:0087089', 'abnormal axial skeleton plus cranial skeleton morphology'),
(369513, 'HP:0005765', 'Sacral meningocele', 'XPO:0100253', 'abnormal vertebra', 0.4166666666666667, 8.05344015541032, 1.8318297040812228, 'UPHENO:0002813', 'abnormal vertebral column'),
(369514, 'HP:0005765', 'Sacral meningocele', 'XPO:0102093', 'abnormal craniofacial skeleton morphology', 0.42857142857142855, 6.211345574613551, 1.6315652749010534, 'UPHENO:0087089', 'abnormal axial skeleton plus cranial skeleton morphology'),
(369515, 'HP:0005765', 'Sacral meningocele', 'XPO:0130368', 'increased size of the elastica externa', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(369516, 'HP:0005765', 'Sacral meningocele', 'XPO:0100226', 'abnormal vertebral element', 0.5102040816326531, 8.05344015541032, 2.0270416962841815, 'UPHENO:0002813', 'abnormal vertebral column'),
(369517, 'HP:0005765', 'Sacral meningocele', 'XPO:0102130', 'abnormal endoskeleton morphology', 0.43478260869565216, 4.638757693672553, 1.4201588541997616, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(369518, 'HP:0005765', 'Sacral meningocele', 'XPO:0102010', 'abnormal perichondrium morphology', 0.45454545454545453, 4.638757693672553, 1.452076521536181, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(369519, 'HP:0005765', 'Sacral meningocele', 'XPO:0141723', 'abnormal posterior notochord morphology', 0.46511627906976744, 4.638757693672553, 1.4688640910537754, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(369520, 'HP:0005765', 'Sacral meningocele', 'XPO:0129707', 'increased size of the vertebral column', 0.4642857142857143, 8.361863005979023, 1.9703536582274415, 'UPHENO:0076695', 'abnormal vertebral column morphology'),
(369521, 'HP:0005765', 'Sacral meningocele', 'XPO:0141699', 'abnormally necrotic anterior notochord', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(369522, 'HP:0005765', 'Sacral meningocele', 'XPO:0102461', 'abnormal postcranial axial skeleton morphology', 0.48936170212765956, 6.272837960958401, 1.7520521287180928, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(369523, 'HP:0005765', 'Sacral meningocele', 'XPO:0140019', 'abnormally necrotic skeletal system', 0.43478260869565216, 4.638757693672553, 1.4201588541997616, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(369524, 'HP:0005765', 'Sacral meningocele', 'XPO:0101957', 'abnormal axial skeleton morphology', 0.45652173913043476, 6.211345574613551, 1.6839282300806968, 'UPHENO:0087089', 'abnormal axial skeleton plus cranial skeleton morphology'),
(369525, 'HP:0005765', 'Sacral meningocele', 'XPO:0140683', 'abnormally necrotic flexural organ', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(369526, 'HP:0005765', 'Sacral meningocele', 'XPO:0107372', 'abnormal flexural organ morphology', 0.46511627906976744, 4.638757693672553, 1.4688640910537754, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(369527, 'HP:0005765', 'Sacral meningocele', 'XPO:0128227', 'decreased size of the vertebral column', 0.4642857142857143, 8.361863005979023, 1.9703536582274415, 'UPHENO:0076695', 'abnormal vertebral column morphology'),
(369528, 'HP:0005765', 'Sacral meningocele', 'XPO:0141703', 'abnormally necrotic posterior notochord', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(369529, 'HP:0005765', 'Sacral meningocele', 'XPO:0139998', 'abnormally necrotic axial skeleton', 0.40384615384615385, 6.211345574613551, 1.5838017617482976, 'UPHENO:0087089', 'abnormal axial skeleton plus cranial skeleton morphology'),
(369530, 'HP:0005765', 'Sacral meningocele', 'XPO:0139774', 'abnormally necrotic elastica externa', 0.43478260869565216, 4.638757693672553, 1.4201588541997616, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(369531, 'HP:0005765', 'Sacral meningocele', 'XPO:0100895', 'abnormal presacral vertebra', 0.4098360655737705, 8.05344015541032, 1.816752660002781, 'UPHENO:0002813', 'abnormal vertebral column'),
(369532, 'HP:0005765', 'Sacral meningocele', 'XPO:0102806', 'abnormal articular system morphology', 0.47619047619047616, 4.638757693672553, 1.4862477031377266, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(369533, 'HP:0005765', 'Sacral meningocele', 'XPO:0127548', 'abnormally localised vertebral element', 0.4166666666666667, 8.05344015541032, 1.8318297040812228, 'UPHENO:0002813', 'abnormal vertebral column'),
(369534, 'HP:0005765', 'Sacral meningocele', 'XPO:0139795', 'abnormally necrotic vertebral element', 0.40625, 8.361863005979023, 1.843097079965941, 'UPHENO:0076695', 'abnormal vertebral column morphology'),
(369535, 'HP:0005765', 'Sacral meningocele', 'XPO:0102728', 'abnormal tendon morphology', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(369536, 'HP:0005765', 'Sacral meningocele', 'XPO:0101860', 'abnormal skeletal subdivision morphology', 0.45454545454545453, 4.638757693672553, 1.452076521536181, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(369537, 'HP:0005765', 'Sacral meningocele', 'XPO:0101226', 'abnormal postsacral vertebra', 0.4098360655737705, 8.05344015541032, 1.816752660002781, 'UPHENO:0002813', 'abnormal vertebral column'),
(369538, 'HP:0005765', 'Sacral meningocele', 'XPO:0102144', 'abnormal cranial skeleton morphology', 0.44680851063829785, 6.211345574613551, 1.665917784661915, 'UPHENO:0087089', 'abnormal axial skeleton plus cranial skeleton morphology'),
(369539, 'HP:0005765', 'Sacral meningocele', 'XPO:0129786', 'increased size of the articular system', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(369540, 'HP:0005765', 'Sacral meningocele', 'XPO:0100584', 'abnormal vertebral column', 0.5813953488372093, 8.05344015541032, 2.163846724815409, 'UPHENO:0002813', 'abnormal vertebral column'),
(369541, 'HP:0005765', 'Sacral meningocele', 'XPO:0103218', 'abnormal joint morphology', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(369542, 'HP:0005765', 'Sacral meningocele', 'XPO:0139917', 'abnormally necrotic notochord', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(369543, 'HP:0005765', 'Sacral meningocele', 'XPO:0140510', 'abnormally necrotic postcranial axial skeleton', 0.4339622641509434, 6.272837960958401, 1.6499015013598524, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(369544, 'HP:0005765', 'Sacral meningocele', 'XPO:0102980', 'abnormal perichordal tissue morphology', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(369545, 'HP:0005765', 'Sacral meningocele', 'XPO:0102325', 'abnormal vertebral centrum morphology', 0.45614035087719296, 8.361863005979023, 1.9529933757015898, 'UPHENO:0076695', 'abnormal vertebral column morphology'),
(369546, 'HP:0005765', 'Sacral meningocele', 'XPO:0141719', 'abnormal anterior notochord morphology', 0.46511627906976744, 4.638757693672553, 1.4688640910537754, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(369547, 'HP:0005765', 'Sacral meningocele', 'XPO:0140432', 'abnormally necrotic skeleton', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(369548, 'HP:0005765', 'Sacral meningocele', 'XPO:0101982', 'abnormal appendicular skeleton morphology', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(369549, 'HP:0005765', 'Sacral meningocele', 'XPO:0102542', 'abnormal vacuolated notochordal tissue morphology', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(369550, 'HP:0005765', 'Sacral meningocele', 'XPO:0102567', 'abnormal skeleton morphology', 0.46511627906976744, 4.638757693672553, 1.4688640910537754, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(369551, 'HP:0005765', 'Sacral meningocele', 'XPO:0102828', 'abnormal occipital region morphology', 0.40350877192982454, 6.272837960958401, 1.5909573036826314, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(369552, 'HP:0005765', 'Sacral meningocele', 'XPO:0101446', 'abnormal transverse process', 0.4032258064516129, 8.05344015541032, 1.8020418700394085, 'UPHENO:0002813', 'abnormal vertebral column'),
(369553, 'HP:0005765', 'Sacral meningocele', 'XPO:0102216', 'abnormal vertebral column morphology', 0.5416666666666666, 8.361863005979023, 2.1282251905218983, 'UPHENO:0076695', 'abnormal vertebral column morphology'),
(369554, 'HP:0005765', 'Sacral meningocele', 'XPO:0128890', 'decreased size of the elastica externa', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(369555, 'HP:0005765', 'Sacral meningocele', 'XPO:0140103', 'abnormally necrotic vertebral column', 0.48148148148148145, 8.361863005979023, 2.006509952146755, 'UPHENO:0076695', 'abnormal vertebral column morphology'),
(369556, 'HP:0005765', 'Sacral meningocele', 'XPO:0102097', 'abnormal skeletal system morphology', 0.4878048780487805, 4.638757693672553, 1.5042634845863214, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(369557, 'HP:0005765', 'Sacral meningocele', 'XPO:0139771', 'abnormally necrotic skeletal subdivision', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(369558, 'HP:0005765', 'Sacral meningocele', 'XPO:0102605', 'abnormal dermal skeleton morphology', 0.43478260869565216, 4.638757693672553, 1.4201588541997616, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(369559, 'HP:0005765', 'Sacral meningocele', 'XPO:0129832', 'increased size of the skeletal system', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(369560, 'HP:0005765', 'Sacral meningocele', 'XPO:0101070', 'abnormal rib', 0.4032258064516129, 8.05344015541032, 1.8020418700394085, 'UPHENO:0002813', 'abnormal vertebral column'),
(369561, 'HP:0005765', 'Sacral meningocele', 'XPO:0125260', 'absent vertebral column', 0.45454545454545453, 8.05344015541032, 1.913283725978873, 'UPHENO:0002813', 'abnormal vertebral column'),
(369562, 'HP:0004836', 'Acute promyelocytic leukemia', 'XPO:0101107', 'abnormal erythroid cell', 0.40540540540540543, 5.574066539846944, 1.5032487170602729, 'UPHENO:0004459', 'abnormal hematopoietic system'),
(369563, 'HP:0004836', 'Acute promyelocytic leukemia', 'XPO:0101587', 'abnormal hemangioblast', 0.40540540540540543, 5.574066539846944, 1.5032487170602729, 'UPHENO:0004459', 'abnormal hematopoietic system'),
(369564, 'HP:0004836', 'Acute promyelocytic leukemia', 'XPO:0100449', 'abnormal lymphocyte', 0.40540540540540543, 5.64885357140806, 1.5132996306721471, 'HP:0002715', 'Abnormality of the immune system'),
(369565, 'HP:0004836', 'Acute promyelocytic leukemia', 'XPO:0141497', 'abnormal lymphoblast', 0.40540540540540543, 5.64885357140806, 1.5132996306721471, 'HP:0002715', 'Abnormality of the immune system'),
(369566, 'HP:0004836', 'Acute promyelocytic leukemia', 'XPO:0101450', 'abnormal myeloid cell', 0.40540540540540543, 5.574066539846944, 1.5032487170602729, 'HP:0001871', 'Abnormality of blood and blood-forming tissues'),
(369567, 'HP:0031528', 'Subretinal deposits', 'XPO:0103048', 'abnormal cornea morphology', 0.45454545454545453, 6.887869297006056, 1.769420718895678, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(369568, 'HP:0031528', 'Subretinal deposits', 'XPO:0103210', 'abnormal pupil morphology', 0.4430379746835443, 6.887869297006056, 1.7468794071802813, 'HP:0012372', 'Abnormal eye morphology'),
(369569, 'HP:0031528', 'Subretinal deposits', 'XPO:0130257', 'increased size of the retinal blood vessel', 0.4574468085106383, 8.040873045973026, 1.9178820903589395, 'HP:0000479', 'Abnormal retinal morphology'),
(369570, 'HP:0031528', 'Subretinal deposits', 'XPO:0103186', 'abnormal peripheral retina morphology', 0.6056338028169014, 8.040873045973026, 2.206767890105474, 'HP:0000479', 'Abnormal retinal morphology'),
(369571, 'HP:0031528', 'Subretinal deposits', 'XPO:0129947', 'increased size of the lens', 0.43209876543209874, 6.887869297006056, 1.7251781994025936, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(369572, 'HP:0031528', 'Subretinal deposits', 'XPO:0141333', 'increased pigmentation in the retinal pigmented epithelium', 0.5058823529411764, 8.040873045973026, 2.0168628550791743, 'HP:0000479', 'Abnormal retinal morphology'),
(369573, 'HP:0031528', 'Subretinal deposits', 'XPO:0130614', 'increased size of the retinal progenitor cell', 0.4574468085106383, 8.040873045973026, 1.9178820903589395, 'HP:0000479', 'Abnormal retinal morphology'),
(369574, 'HP:0031528', 'Subretinal deposits', 'XPO:0129062', 'decreased size of the ciliary body', 0.4117647058823529, 6.887869297006056, 1.6840966347682629, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(369575, 'HP:0031528', 'Subretinal deposits', 'XPO:0141182', 'abnormally necrotic inner limiting membrane', 0.48314606741573035, 8.040873045973026, 1.9710190741722953, 'HP:0000479', 'Abnormal retinal morphology'),
(369576, 'HP:0031528', 'Subretinal deposits', 'XPO:0128431', 'decreased size of the retinal inner nuclear layer', 0.4777777777777778, 8.040873045973026, 1.960038381077836, 'HP:0000479', 'Abnormal retinal morphology'),
(369577, 'HP:0031528', 'Subretinal deposits', 'XPO:0141141', 'abnormally necrotic cornea', 0.42168674698795183, 6.887869297006056, 1.7042661756699493, 'HP:0012372', 'Abnormal eye morphology'),
(369578, 'HP:0031528', 'Subretinal deposits', 'XPO:0128330', 'decreased size of the retinal progenitor cell region', 0.5584415584415584, 8.040873045973026, 2.1190464070010115, 'HP:0000479', 'Abnormal retinal morphology'),
(369579, 'HP:0031528', 'Subretinal deposits', 'XPO:0102963', 'abnormal retinal outer nuclear layer morphology', 0.524390243902439, 8.040873045973026, 2.053425279323877, 'HP:0000479', 'Abnormal retinal morphology'),
(369580, 'HP:0031528', 'Subretinal deposits', 'XPO:0102805', 'abnormal retinal layer morphology', 0.6515151515151515, 8.040873045973026, 2.288831715277734, 'HP:0000479', 'Abnormal retinal morphology'),
(369581, 'HP:0031528', 'Subretinal deposits', 'XPO:0141138', 'abnormally necrotic retinal inner plexiform layer', 0.48314606741573035, 8.040873045973026, 1.9710190741722953, 'HP:0000479', 'Abnormal retinal morphology'),
(369582, 'HP:0031528', 'Subretinal deposits', 'XPO:0102476', 'abnormal lens transitional zone morphology', 0.4666666666666667, 6.887869297006056, 1.7928577760852904, 'HP:0012372', 'Abnormal eye morphology'),
(369583, 'HP:0031528', 'Subretinal deposits', 'XPO:0100779', 'abnormal optic choroid vascular plexus', 0.4696969696969697, 6.887869297006056, 1.7986693238259617, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(369584, 'HP:0031528', 'Subretinal deposits', 'XPO:0102939', 'abnormal retinal ganglion cell layer morphology', 0.524390243902439, 8.040873045973026, 2.053425279323877, 'HP:0000479', 'Abnormal retinal morphology'),
(369585, 'HP:0031528', 'Subretinal deposits', 'XPO:0128052', 'decreased size of the iris', 0.4069767441860465, 6.887869297006056, 1.6742767456052652, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(369586, 'HP:0031528', 'Subretinal deposits', 'XPO:0107252', 'decreased size of the globe', 0.41333333333333333, 6.575878401988876, 1.6486448190828538, 'UPHENO:0087924', 'abnormal camera-type eye morphology'),
(369587, 'HP:0031528', 'Subretinal deposits', 'XPO:0130326', 'increased size of the retinal cone cell', 0.43, 8.040873045973026, 1.859455675666511, 'HP:0000479', 'Abnormal retinal morphology'),
(369588, 'HP:0031528', 'Subretinal deposits', 'XPO:0128521', 'decreased size of the horizontal cell', 0.43434343434343436, 8.040873045973026, 1.8688232698432123, 'HP:0000479', 'Abnormal retinal morphology'),
(369589, 'HP:0031528', 'Subretinal deposits', 'XPO:0129681', 'increased size of the eye photoreceptor cell', 0.44329896907216493, 8.040873045973026, 1.8879911895239345, 'HP:0000479', 'Abnormal retinal morphology'),
(369590, 'HP:0031528', 'Subretinal deposits', 'XPO:0133372', 'eye fused with olfactory epithelium', 0.4861111111111111, 6.887869297006056, 1.8298278053291577, 'HP:0012372', 'Abnormal eye morphology'),
(369591, 'HP:0031528', 'Subretinal deposits', 'XPO:0129780', 'increased size of the retina', 0.5733333333333334, 8.040873045973026, 2.147114469784475, 'HP:0000479', 'Abnormal retinal morphology'),
(369592, 'HP:0031528', 'Subretinal deposits', 'XPO:0130413', 'increased size of the central retina', 0.589041095890411, 8.040873045973026, 2.1763282544036455, 'HP:0000479', 'Abnormal retinal morphology'),
(369593, 'HP:0031528', 'Subretinal deposits', 'XPO:0130189', 'increased size of the optic chiasm', 0.45555555555555555, 7.796308075334707, 1.884582568247241, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(369594, 'HP:0031528', 'Subretinal deposits', 'XPO:0130845', 'increased size of the retinal outer plexiform layer', 0.4777777777777778, 8.040873045973026, 1.960038381077836, 'HP:0000479', 'Abnormal retinal morphology'),
(369595, 'HP:0031528', 'Subretinal deposits', 'XPO:0141337', 'increased pigmentation in the eye', 0.4861111111111111, 6.887869297006056, 1.8298278053291577, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(369596, 'HP:0031528', 'Subretinal deposits', 'XPO:0140218', 'abnormally necrotic sclera', 0.4666666666666667, 6.887869297006056, 1.7928577760852904, 'HP:0012372', 'Abnormal eye morphology'),
(369597, 'HP:0031528', 'Subretinal deposits', 'XPO:0129741', 'increased size of the optic fiber layer', 0.4777777777777778, 8.040873045973026, 1.960038381077836, 'HP:0000479', 'Abnormal retinal morphology'),
(369598, 'HP:0031528', 'Subretinal deposits', 'XPO:0130125', 'increased size of the outer limiting membrane', 0.4777777777777778, 8.040873045973026, 1.960038381077836, 'HP:0000479', 'Abnormal retinal morphology'),
(369599, 'HP:0031528', 'Subretinal deposits', 'XPO:0128295', 'decreased size of the retinal neural layer', 0.4777777777777778, 8.040873045973026, 1.960038381077836, 'HP:0000479', 'Abnormal retinal morphology'),
(369600, 'HP:0031528', 'Subretinal deposits', 'XPO:0129371', 'decreased size of the retinal outer plexiform layer', 0.4777777777777778, 8.040873045973026, 1.960038381077836, 'HP:0000479', 'Abnormal retinal morphology'),
(369601, 'HP:0031528', 'Subretinal deposits', 'XPO:0130515', 'increased size of the retinal outer nuclear layer', 0.4777777777777778, 8.040873045973026, 1.960038381077836, 'HP:0000479', 'Abnormal retinal morphology'),
(369602, 'HP:0031528', 'Subretinal deposits', 'XPO:0102441', 'abnormal retinal inner plexiform layer morphology', 0.524390243902439, 8.040873045973026, 2.053425279323877, 'HP:0000479', 'Abnormal retinal morphology'),
(369603, 'HP:0031528', 'Subretinal deposits', 'XPO:0102581', 'abnormal outer limiting membrane morphology', 0.524390243902439, 8.040873045973026, 2.053425279323877, 'HP:0000479', 'Abnormal retinal morphology'),
(369604, 'HP:0031528', 'Subretinal deposits', 'XPO:0102882', 'abnormal retinal cone cell morphology', 0.4942528735632184, 8.040873045973026, 1.9935457378573478, 'HP:0000479', 'Abnormal retinal morphology'),
(369605, 'HP:0031528', 'Subretinal deposits', 'XPO:0130362', 'increased size of the retinal pigmented epithelium', 0.4725274725274725, 8.040873045973026, 1.9492391893577128, 'HP:0000479', 'Abnormal retinal morphology'),
(369606, 'HP:0031528', 'Subretinal deposits', 'XPO:0128875', 'decreased size of the photoreceptor layer', 0.48314606741573035, 8.040873045973026, 1.9710190741722953, 'HP:0000479', 'Abnormal retinal morphology'),
(369607, 'HP:0031528', 'Subretinal deposits', 'XPO:0140317', 'abnormally necrotic retinal progenitor cell', 0.5, 8.040873045973026, 2.0051026215599324, 'HP:0000479', 'Abnormal retinal morphology'),
(369608, 'HP:0031528', 'Subretinal deposits', 'XPO:0103780', 'decreased size of the bipolar neuron in the retinal inner plexiform layer', 0.4056603773584906, 8.040873045973026, 1.8060630094548564, 'HP:0000479', 'Abnormal retinal morphology'),
(369609, 'HP:0031528', 'Subretinal deposits', 'XPO:0130863', 'increased size of the sclera', 0.45454545454545453, 6.887869297006056, 1.769420718895678, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(369610, 'HP:0031528', 'Subretinal deposits', 'XPO:0102117', 'abnormal retina morphology', 0.6323529411764706, 8.040873045973026, 2.2549212226256703, 'HP:0000479', 'Abnormal retinal morphology'),
(369611, 'HP:0031528', 'Subretinal deposits', 'XPO:0103184', 'abnormal inner limiting membrane morphology', 0.524390243902439, 8.040873045973026, 2.053425279323877, 'HP:0000479', 'Abnormal retinal morphology'),
(369612, 'HP:0031528', 'Subretinal deposits', 'XPO:0129971', 'increased size of the retinal ganglion cell', 0.42574257425742573, 8.040873045973026, 1.850227550835222, 'HP:0000479', 'Abnormal retinal morphology'),
(369613, 'HP:0031528', 'Subretinal deposits', 'XPO:0127907', 'abnormally localised optic choroid vascular plexus', 0.4025974025974026, 6.887869297006056, 1.6652442128423794, 'HP:0012372', 'Abnormal eye morphology'),
(369614, 'HP:0031528', 'Subretinal deposits', 'XPO:0140081', 'abnormally necrotic amacrine cell', 0.45263157894736844, 8.040873045973026, 1.9077612698957138, 'HP:0000479', 'Abnormal retinal morphology'),
(369615, 'HP:0031528', 'Subretinal deposits', 'XPO:0130734', 'increased size of the amacrine cell', 0.4174757281553398, 8.040873045973026, 1.8321761186829812, 'HP:0000479', 'Abnormal retinal morphology'),
(369616, 'HP:0031528', 'Subretinal deposits', 'XPO:0102266', 'abnormal horizontal cell morphology', 0.5, 8.040873045973026, 2.0051026215599324, 'HP:0000479', 'Abnormal retinal morphology'),
(369617, 'HP:0031528', 'Subretinal deposits', 'XPO:0128935', 'decreased size of the central retina', 0.589041095890411, 8.040873045973026, 2.1763282544036455, 'HP:0000479', 'Abnormal retinal morphology'),
(369618, 'HP:0031528', 'Subretinal deposits', 'XPO:0115417', 'abnormally wholly ventralized eye', 0.4605263157894737, 6.887869297006056, 1.7810236020304815, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(369619, 'HP:0031528', 'Subretinal deposits', 'XPO:0129911', 'increased size of the retinal inner nuclear layer', 0.4777777777777778, 8.040873045973026, 1.960038381077836, 'HP:0000479', 'Abnormal retinal morphology'),
(369620, 'HP:0031528', 'Subretinal deposits', 'XPO:0103926', 'decreased pigmentation in the retinal pigmented epithelium', 0.5058823529411764, 8.040873045973026, 2.0168628550791743, 'HP:0000479', 'Abnormal retinal morphology'),
(369621, 'HP:0031528', 'Subretinal deposits', 'XPO:0140799', 'abnormally necrotic ciliary body', 0.42168674698795183, 6.887869297006056, 1.7042661756699493, 'HP:0012372', 'Abnormal eye morphology'),
(369622, 'HP:0031528', 'Subretinal deposits', 'XPO:0140473', 'abnormally necrotic lens transitional zone', 0.4375, 6.887869297006056, 1.7359270772241988, 'HP:0012372', 'Abnormal eye morphology'),
(369623, 'HP:0031528', 'Subretinal deposits', 'XPO:0102818', 'abnormal optic chiasm morphology', 0.5061728395061729, 7.796308075334707, 1.9865244514370002, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(369624, 'HP:0031528', 'Subretinal deposits', 'XPO:0128779', 'decreased size of the retinal blood vessel', 0.4574468085106383, 8.040873045973026, 1.9178820903589395, 'HP:0000479', 'Abnormal retinal morphology'),
(369625, 'HP:0031528', 'Subretinal deposits', 'XPO:0102946', 'abnormal retinal inner nuclear layer morphology', 0.524390243902439, 8.040873045973026, 2.053425279323877, 'HP:0000479', 'Abnormal retinal morphology'),
(369626, 'HP:0031528', 'Subretinal deposits', 'XPO:0140869', 'abnormally necrotic optic chiasm', 0.47674418604651164, 7.796308075334707, 1.9279119657140185, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(369627, 'HP:0031528', 'Subretinal deposits', 'XPO:0140820', 'abnormally necrotic globe', 0.4246575342465753, 6.575878401988876, 1.6710763919384135, 'UPHENO:0087924', 'abnormal camera-type eye morphology'),
(369628, 'HP:0031528', 'Subretinal deposits', 'XPO:0129532', 'increased size of the iris', 0.4069767441860465, 6.887869297006056, 1.6742767456052652, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(369629, 'HP:0031528', 'Subretinal deposits', 'XPO:0140553', 'abnormally necrotic retinal stem cell region', 0.5733333333333334, 8.040873045973026, 2.147114469784475, 'HP:0000479', 'Abnormal retinal morphology'),
(369630, 'HP:0031528', 'Subretinal deposits', 'XPO:0103110', 'abnormal lens fiber cell mass morphology', 0.4117647058823529, 6.887869297006056, 1.6840966347682629, 'HP:0012372', 'Abnormal eye morphology'),
(369631, 'HP:0031528', 'Subretinal deposits', 'XPO:0102815', 'abnormal retinal ganglion cell morphology', 0.48863636363636365, 8.040873045973026, 1.982186410418029, 'HP:0000479', 'Abnormal retinal morphology'),
(369632, 'HP:0031528', 'Subretinal deposits', 'XPO:0128646', 'decreased size of the outer limiting membrane', 0.4777777777777778, 8.040873045973026, 1.960038381077836, 'HP:0000479', 'Abnormal retinal morphology'),
(369633, 'HP:0031528', 'Subretinal deposits', 'XPO:0140487', 'abnormally necrotic retinal layer', 0.5972222222222222, 8.040873045973026, 2.191389529299339, 'HP:0000479', 'Abnormal retinal morphology'),
(369634, 'HP:0031528', 'Subretinal deposits', 'XPO:0101861', 'abnormal photoreceptor layer morphology', 0.5308641975308642, 8.040873045973026, 2.066061861851679, 'HP:0000479', 'Abnormal retinal morphology'),
(369635, 'HP:0031528', 'Subretinal deposits', 'XPO:0128710', 'decreased size of the optic chiasm', 0.45555555555555555, 7.796308075334707, 1.884582568247241, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(369636, 'HP:0031528', 'Subretinal deposits', 'XPO:0125589', 'absent hyaloid blood vessel', 0.4025974025974026, 6.887869297006056, 1.6652442128423794, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(369637, 'HP:0031528', 'Subretinal deposits', 'XPO:0128669', 'decreased size of the ciliary marginal zone', 0.5, 8.040873045973026, 2.0051026215599324, 'HP:0000479', 'Abnormal retinal morphology'),
(369638, 'HP:0031528', 'Subretinal deposits', 'XPO:0129419', 'decreased size of the pupil', 0.4117647058823529, 6.887869297006056, 1.6840966347682629, 'HP:0012372', 'Abnormal eye morphology'),
(369639, 'HP:0031528', 'Subretinal deposits', 'XPO:0101817', 'abnormal eye morphology', 0.5072463768115942, 6.887869297006056, 1.8691834433404724, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(369640, 'HP:0031528', 'Subretinal deposits', 'XPO:0102017', 'abnormal retinal neural layer morphology', 0.5308641975308642, 8.040873045973026, 2.066061861851679, 'HP:0000479', 'Abnormal retinal morphology'),
(369641, 'HP:0031528', 'Subretinal deposits', 'XPO:0130265', 'increased size of the peripheral retina', 0.5443037974683544, 8.040873045973026, 2.0920510830006163, 'HP:0000479', 'Abnormal retinal morphology'),
(369642, 'HP:0031528', 'Subretinal deposits', 'XPO:0141323', 'edematous eye', 0.49295774647887325, 6.887869297006056, 1.8426688597502066, 'HP:0012372', 'Abnormal eye morphology'),
(369643, 'HP:0031528', 'Subretinal deposits', 'XPO:0129029', 'decreased size of the Muller cell', 0.48314606741573035, 8.040873045973026, 1.9710190741722953, 'HP:0000479', 'Abnormal retinal morphology'),
(369644, 'HP:0031528', 'Subretinal deposits', 'XPO:0133354', 'fused eyes', 0.4861111111111111, 6.887869297006056, 1.8298278053291577, 'HP:0012372', 'Abnormal eye morphology'),
(369645, 'HP:0031528', 'Subretinal deposits', 'XPO:0103155', 'abnormal bipolar neuron morphology', 0.48314606741573035, 8.040873045973026, 1.9710190741722953, 'HP:0000479', 'Abnormal retinal morphology'),
(369646, 'HP:0031528', 'Subretinal deposits', 'XPO:0140346', 'abnormally necrotic retinal blood vessel', 0.4673913043478261, 8.040873045973026, 1.938616553383523, 'HP:0000479', 'Abnormal retinal morphology'),
(369647, 'HP:0031528', 'Subretinal deposits', 'XPO:0129810', 'increased size of the retinal progenitor cell region', 0.5584415584415584, 8.040873045973026, 2.1190464070010115, 'HP:0000479', 'Abnormal retinal morphology'),
(369648, 'HP:0031528', 'Subretinal deposits', 'XPO:0141338', 'decreased pigmentation in the optic nerve', 0.41836734693877553, 7.796308075334707, 1.8060234564908433, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(369649, 'HP:0031528', 'Subretinal deposits', 'XPO:0140520', 'abnormally necrotic retinal outer nuclear layer', 0.48314606741573035, 8.040873045973026, 1.9710190741722953, 'HP:0000479', 'Abnormal retinal morphology'),
(369650, 'HP:0031528', 'Subretinal deposits', 'XPO:0129138', 'decreased size of the retinal progenitor cell', 0.4574468085106383, 8.040873045973026, 1.9178820903589395, 'HP:0000479', 'Abnormal retinal morphology'),
(369651, 'HP:0031528', 'Subretinal deposits', 'XPO:0101315', 'abnormal hyaloid vascular plexus', 0.4626865671641791, 6.887869297006056, 1.7851959556606887, 'HP:0012372', 'Abnormal eye morphology'),
(369652, 'HP:0031528', 'Subretinal deposits', 'XPO:0139887', 'abnormally necrotic Muller cell', 0.5308641975308642, 8.040873045973026, 2.066061861851679, 'HP:0000479', 'Abnormal retinal morphology'),
(369653, 'HP:0031528', 'Subretinal deposits', 'XPO:0130761', 'increased size of the retinal inner plexiform layer', 0.4777777777777778, 8.040873045973026, 1.960038381077836, 'HP:0000479', 'Abnormal retinal morphology'),
(369654, 'HP:0031528', 'Subretinal deposits', 'XPO:0140375', 'abnormally necrotic lens', 0.44871794871794873, 6.887869297006056, 1.7580416894914344, 'HP:0012372', 'Abnormal eye morphology'),
(369655, 'HP:0031528', 'Subretinal deposits', 'XPO:0128201', 'decreased size of the eye photoreceptor cell', 0.44329896907216493, 8.040873045973026, 1.8879911895239345, 'HP:0000479', 'Abnormal retinal morphology'),
(369656, 'HP:0031528', 'Subretinal deposits', 'XPO:0102239', 'abnormal retinal pigmented epithelium morphology', 0.524390243902439, 8.040873045973026, 2.053425279323877, 'HP:0000479', 'Abnormal retinal morphology'),
(369657, 'HP:0031528', 'Subretinal deposits', 'XPO:0115423', 'abnormally incomplete structure of eye', 0.5, 6.887869297006056, 1.8557841061133777, 'HP:0012372', 'Abnormal eye morphology'),
(369658, 'HP:0031528', 'Subretinal deposits', 'XPO:0133370', 'olfactory pit fused with brain', 0.4307692307692308, 5.788671267106304, 1.5791078078799214, 'UPHENO:0087472', 'abnormal face morphology'),
(369659, 'HP:0031528', 'Subretinal deposits', 'XPO:0129285', 'decreased size of the retinal inner plexiform layer', 0.4777777777777778, 8.040873045973026, 1.960038381077836, 'HP:0000479', 'Abnormal retinal morphology'),
(369660, 'HP:0031528', 'Subretinal deposits', 'XPO:0129258', 'decreased size of the amacrine cell', 0.4174757281553398, 8.040873045973026, 1.8321761186829812, 'HP:0000479', 'Abnormal retinal morphology'),
(369661, 'HP:0031528', 'Subretinal deposits', 'XPO:0141343', 'decreased pigmentation in the eye', 0.4861111111111111, 6.887869297006056, 1.8298278053291577, 'HP:0012372', 'Abnormal eye morphology'),
(369662, 'HP:0031528', 'Subretinal deposits', 'XPO:0140192', 'abnormally necrotic retina', 0.589041095890411, 8.040873045973026, 2.1763282544036455, 'HP:0000479', 'Abnormal retinal morphology'),
(369663, 'HP:0031528', 'Subretinal deposits', 'XPO:0130285', 'increased size of the lens transitional zone', 0.4268292682926829, 6.887869297006056, 1.714626551799759, 'HP:0012372', 'Abnormal eye morphology'),
(369664, 'HP:0031528', 'Subretinal deposits', 'XPO:0133369', 'eye fused with brain', 0.4861111111111111, 6.887869297006056, 1.8298278053291577, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(369665, 'HP:0031528', 'Subretinal deposits', 'XPO:0129680', 'increased size of the retinal rod cell', 0.43, 8.040873045973026, 1.859455675666511, 'HP:0000479', 'Abnormal retinal morphology'),
(369666, 'HP:0031528', 'Subretinal deposits', 'XPO:0130148', 'increased size of the ciliary marginal zone', 0.5, 8.040873045973026, 2.0051026215599324, 'HP:0000479', 'Abnormal retinal morphology'),
(369667, 'HP:0031528', 'Subretinal deposits', 'XPO:0130859', 'increased size of the globe', 0.41333333333333333, 6.575878401988876, 1.6486448190828538, 'UPHENO:0087924', 'abnormal camera-type eye morphology'),
(369668, 'HP:0031528', 'Subretinal deposits', 'XPO:0130560', 'increased size of the bipolar neuron', 0.4174757281553398, 8.040873045973026, 1.8321761186829812, 'HP:0000479', 'Abnormal retinal morphology'),
(369669, 'HP:0031528', 'Subretinal deposits', 'XPO:0103142', 'abnormal optic nerve morphology', 0.43157894736842106, 7.796308075334707, 1.8343179747559781, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(369670, 'HP:0031528', 'Subretinal deposits', 'XPO:0102663', 'abnormal retinal progenitor cell morphology', 0.5308641975308642, 8.040873045973026, 2.066061861851679, 'HP:0000479', 'Abnormal retinal morphology'),
(369671, 'HP:0031528', 'Subretinal deposits', 'XPO:0129388', 'decreased size of the sclera', 0.45454545454545453, 6.887869297006056, 1.769420718895678, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(369672, 'HP:0031528', 'Subretinal deposits', 'XPO:0128100', 'decreased size of the inner limiting membrane', 0.4777777777777778, 8.040873045973026, 1.960038381077836, 'HP:0000479', 'Abnormal retinal morphology'),
(369673, 'HP:0031528', 'Subretinal deposits', 'XPO:0102862', 'abnormal iris morphology', 0.4430379746835443, 6.887869297006056, 1.7468794071802813, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(369674, 'HP:0031528', 'Subretinal deposits', 'XPO:0140464', 'abnormally necrotic retinal pigmented epithelium', 0.4777777777777778, 8.040873045973026, 1.960038381077836, 'HP:0000479', 'Abnormal retinal morphology'),
(369675, 'HP:0031528', 'Subretinal deposits', 'XPO:0128918', 'decreased size of the choroid', 0.4025974025974026, 6.575878401988876, 1.627092979653308, 'UPHENO:0087924', 'abnormal camera-type eye morphology'),
(369676, 'HP:0031528', 'Subretinal deposits', 'XPO:0140489', 'abnormally necrotic ciliary marginal zone', 0.5119047619047619, 8.040873045973026, 2.028832472656439, 'HP:0000479', 'Abnormal retinal morphology'),
(369677, 'HP:0031528', 'Subretinal deposits', 'XPO:0129775', 'increased size of the retinal neural layer', 0.4777777777777778, 8.040873045973026, 1.960038381077836, 'HP:0000479', 'Abnormal retinal morphology'),
(369678, 'HP:0031528', 'Subretinal deposits', 'XPO:0128475', 'decreased size of the retinal stem cell region', 0.5584415584415584, 8.040873045973026, 2.1190464070010115, 'HP:0000479', 'Abnormal retinal morphology'),
(369679, 'HP:0031528', 'Subretinal deposits', 'XPO:0103226', 'abnormal retinal outer plexiform layer morphology', 0.524390243902439, 8.040873045973026, 2.053425279323877, 'HP:0000479', 'Abnormal retinal morphology'),
(369680, 'HP:0031528', 'Subretinal deposits', 'XPO:0140240', 'abnormally necrotic eye photoreceptor cell', 0.48314606741573035, 8.040873045973026, 1.9710190741722953, 'HP:0000479', 'Abnormal retinal morphology'),
(369681, 'HP:0031528', 'Subretinal deposits', 'XPO:0101961', 'abnormal retinal blood vessel morphology', 0.5058823529411764, 8.040873045973026, 2.0168628550791743, 'HP:0000479', 'Abnormal retinal morphology'),
(369682, 'HP:0031528', 'Subretinal deposits', 'XPO:0102212', 'abnormal globe morphology', 0.45588235294117646, 6.575878401988876, 1.7314233793482612, 'UPHENO:0087924', 'abnormal camera-type eye morphology'),
(369683, 'HP:0031528', 'Subretinal deposits', 'XPO:0102723', 'abnormal lower eyelid morphology', 0.40789473684210525, 6.575878401988876, 1.6377625561371638, 'UPHENO:0087924', 'abnormal camera-type eye morphology'),
(369684, 'HP:0031528', 'Subretinal deposits', 'XPO:0130893', 'increased size of the pupil', 0.4166666666666667, 6.887869297006056, 1.6940913612964297, 'HP:0012372', 'Abnormal eye morphology'),
(369685, 'HP:0031528', 'Subretinal deposits', 'XPO:0133371', 'eye fused with olfactory pit', 0.4861111111111111, 6.887869297006056, 1.8298278053291577, 'HP:0012372', 'Abnormal eye morphology'),
(369686, 'HP:0031528', 'Subretinal deposits', 'XPO:0103160', 'abnormal choroid morphology', 0.44285714285714284, 6.575878401988876, 1.7065095138559256, 'UPHENO:0087924', 'abnormal camera-type eye morphology'),
(369687, 'HP:0031528', 'Subretinal deposits', 'XPO:0102513', 'abnormal sclera morphology', 0.5, 6.887869297006056, 1.8557841061133777, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(369688, 'HP:0031528', 'Subretinal deposits', 'XPO:0102226', 'abnormal Jacobsons organ morphology', 0.4375, 5.788671267106304, 1.5913967699348293, 'UPHENO:0087472', 'abnormal face morphology'),
(369689, 'HP:0031528', 'Subretinal deposits', 'XPO:0139912', 'abnormally necrotic optic fiber layer', 0.48314606741573035, 8.040873045973026, 1.9710190741722953, 'HP:0000479', 'Abnormal retinal morphology'),
(369690, 'HP:0031528', 'Subretinal deposits', 'XPO:0128501', 'decreased size of the retinal ganglion cell layer', 0.4777777777777778, 8.040873045973026, 1.960038381077836, 'HP:0000479', 'Abnormal retinal morphology'),
(369691, 'HP:0031528', 'Subretinal deposits', 'XPO:0102996', 'abnormal optic fiber layer morphology', 0.524390243902439, 8.040873045973026, 2.053425279323877, 'HP:0000479', 'Abnormal retinal morphology'),
(369692, 'HP:0031528', 'Subretinal deposits', 'XPO:0102196', 'abnormal central retina morphology', 0.6323529411764706, 8.040873045973026, 2.2549212226256703, 'HP:0000479', 'Abnormal retinal morphology'),
(369693, 'HP:0031528', 'Subretinal deposits', 'XPO:0129981', 'increased size of the retinal ganglion cell layer', 0.4777777777777778, 8.040873045973026, 1.960038381077836, 'HP:0000479', 'Abnormal retinal morphology'),
(369694, 'HP:0031528', 'Subretinal deposits', 'XPO:0102162', 'abnormal ciliary marginal zone morphology', 0.5657894736842105, 8.040873045973026, 2.1329419421640696, 'HP:0000479', 'Abnormal retinal morphology'),
(369695, 'HP:0031528', 'Subretinal deposits', 'XPO:0130122', 'increased size of the retinal layer', 0.589041095890411, 8.040873045973026, 2.1763282544036455, 'HP:0000479', 'Abnormal retinal morphology'),
(369696, 'HP:0031528', 'Subretinal deposits', 'XPO:0140391', 'abnormally necrotic central retina', 0.6056338028169014, 8.040873045973026, 2.206767890105474, 'HP:0000479', 'Abnormal retinal morphology'),
(369697, 'HP:0031528', 'Subretinal deposits', 'XPO:0103814', 'decreased length of axon in retinal ganglion cell', 0.43, 8.040873045973026, 1.859455675666511, 'HP:0000479', 'Abnormal retinal morphology'),
(369698, 'HP:0031528', 'Subretinal deposits', 'XPO:0100371', 'abnormal hyaloid blood vessel', 0.47692307692307695, 6.887869297006056, 1.8124524320853552, 'HP:0012372', 'Abnormal eye morphology'),
(369699, 'HP:0031528', 'Subretinal deposits', 'XPO:0128568', 'decreased size of the optic disc', 0.43661971830985913, 6.575878401988876, 1.6944492248268372, 'UPHENO:0087924', 'abnormal camera-type eye morphology'),
(369700, 'HP:0031528', 'Subretinal deposits', 'XPO:0141156', 'abnormally necrotic outer limiting membrane', 0.48314606741573035, 8.040873045973026, 1.9710190741722953, 'HP:0000479', 'Abnormal retinal morphology'),
(369701, 'HP:0031528', 'Subretinal deposits', 'XPO:0102966', 'abnormal olfactory pit morphology', 0.45161290322580644, 5.788671267106304, 1.6168607351153301, 'UPHENO:0087472', 'abnormal face morphology'),
(369702, 'HP:0031528', 'Subretinal deposits', 'XPO:0103706', 'increased pigmentation in the optic nerve', 0.41836734693877553, 7.796308075334707, 1.8060234564908433, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(369703, 'HP:0031528', 'Subretinal deposits', 'XPO:0102505', 'abnormal retinal stem cell region morphology', 0.5972222222222222, 8.040873045973026, 2.191389529299339, 'HP:0000479', 'Abnormal retinal morphology'),
(369704, 'HP:0031528', 'Subretinal deposits', 'XPO:0127563', 'abnormally localised retinal blood vessel', 0.5584415584415584, 8.040873045973026, 2.1190464070010115, 'HP:0000479', 'Abnormal retinal morphology'),
(369705, 'HP:0031528', 'Subretinal deposits', 'XPO:0129955', 'increased size of the retinal stem cell region', 0.5584415584415584, 8.040873045973026, 2.1190464070010115, 'HP:0000479', 'Abnormal retinal morphology'),
(369706, 'HP:0031528', 'Subretinal deposits', 'XPO:0102756', 'abnormal Muller cell morphology', 0.5657894736842105, 8.040873045973026, 2.1329419421640696, 'HP:0000479', 'Abnormal retinal morphology'),
(369707, 'HP:0031528', 'Subretinal deposits', 'XPO:0128261', 'decreased size of the optic fiber layer', 0.4777777777777778, 8.040873045973026, 1.960038381077836, 'HP:0000479', 'Abnormal retinal morphology'),
(369708, 'HP:0031528', 'Subretinal deposits', 'XPO:0140945', 'abnormally necrotic retinal ganglion cell layer', 0.48314606741573035, 8.040873045973026, 1.9710190741722953, 'HP:0000479', 'Abnormal retinal morphology'),
(369709, 'HP:0031528', 'Subretinal deposits', 'XPO:0103376', 'increased size of the eye', 0.4375, 6.887869297006056, 1.7359270772241988, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(369710, 'HP:0031528', 'Subretinal deposits', 'XPO:0101359', 'abnormal hyaloid artery', 0.45454545454545453, 6.887869297006056, 1.769420718895678, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(369711, 'HP:0031528', 'Subretinal deposits', 'XPO:0127230', 'abnormally localised hyaloid blood vessel', 0.4189189189189189, 6.887869297006056, 1.6986638159319787, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(369712, 'HP:0031528', 'Subretinal deposits', 'XPO:0139731', 'abnormally necrotic eye', 0.4605263157894737, 6.887869297006056, 1.7810236020304815, 'HP:0012372', 'Abnormal eye morphology'),
(369713, 'HP:0031528', 'Subretinal deposits', 'XPO:0141014', 'abnormally necrotic retinal outer plexiform layer', 0.48314606741573035, 8.040873045973026, 1.9710190741722953, 'HP:0000479', 'Abnormal retinal morphology'),
(369714, 'HP:0031528', 'Subretinal deposits', 'XPO:0128599', 'decreased size of the olfactory pit', 0.417910447761194, 5.788671267106304, 1.5553604730668558, 'UPHENO:0087472', 'abnormal face morphology'),
(369715, 'HP:0031528', 'Subretinal deposits', 'XPO:0128467', 'decreased size of the lens', 0.43209876543209874, 6.887869297006056, 1.7251781994025936, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(369716, 'HP:0031528', 'Subretinal deposits', 'XPO:0140250', 'abnormally necrotic iris', 0.4166666666666667, 6.887869297006056, 1.6940913612964297, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(369717, 'HP:0031528', 'Subretinal deposits', 'XPO:0140531', 'abnormally necrotic retinal progenitor cell region', 0.5733333333333334, 8.040873045973026, 2.147114469784475, 'HP:0000479', 'Abnormal retinal morphology'),
(369718, 'HP:0031528', 'Subretinal deposits', 'XPO:0100329', 'abnormal retinal blood vessel', 0.6417910447761194, 8.040873045973026, 2.2716866670135576, 'HP:0000479', 'Abnormal retinal morphology'),
(369719, 'HP:0031528', 'Subretinal deposits', 'XPO:0130506', 'increased size of the Muller cell', 0.48314606741573035, 8.040873045973026, 1.9710190741722953, 'HP:0000479', 'Abnormal retinal morphology'),
(369720, 'HP:0031528', 'Subretinal deposits', 'XPO:0128848', 'decreased size of the retinal cone cell', 0.43, 8.040873045973026, 1.859455675666511, 'HP:0000479', 'Abnormal retinal morphology'),
(369721, 'HP:0031528', 'Subretinal deposits', 'XPO:0141033', 'abnormally necrotic photoreceptor layer', 0.48863636363636365, 8.040873045973026, 1.982186410418029, 'HP:0000479', 'Abnormal retinal morphology'),
(369722, 'HP:0031528', 'Subretinal deposits', 'XPO:0128300', 'decreased size of the retina', 0.5733333333333334, 8.040873045973026, 2.147114469784475, 'HP:0000479', 'Abnormal retinal morphology'),
(369723, 'HP:0031528', 'Subretinal deposits', 'XPO:0101823', 'abnormal lens epithelium morphology', 0.4268292682926829, 6.887869297006056, 1.714626551799759, 'HP:0012372', 'Abnormal eye morphology'),
(369724, 'HP:0031528', 'Subretinal deposits', 'XPO:0129038', 'decreased size of the retinal outer nuclear layer', 0.4777777777777778, 8.040873045973026, 1.960038381077836, 'HP:0000479', 'Abnormal retinal morphology'),
(369725, 'HP:0031528', 'Subretinal deposits', 'XPO:0140271', 'abnormally necrotic peripheral retina', 0.5584415584415584, 8.040873045973026, 2.1190464070010115, 'HP:0000479', 'Abnormal retinal morphology'),
(369726, 'HP:0031528', 'Subretinal deposits', 'XPO:0125932', 'absent retinal pigmented epithelium', 0.40625, 7.796308075334707, 1.7796769806919246, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(369727, 'HP:0031528', 'Subretinal deposits', 'XPO:0103086', 'abnormal amacrine cell morphology', 0.48314606741573035, 8.040873045973026, 1.9710190741722953, 'HP:0000479', 'Abnormal retinal morphology'),
(369728, 'HP:0031528', 'Subretinal deposits', 'XPO:0130001', 'increased size of the horizontal cell', 0.43434343434343436, 8.040873045973026, 1.8688232698432123, 'HP:0000479', 'Abnormal retinal morphology'),
(369729, 'HP:0031528', 'Subretinal deposits', 'XPO:0128200', 'decreased size of the retinal rod cell', 0.43, 8.040873045973026, 1.859455675666511, 'HP:0000479', 'Abnormal retinal morphology'),
(369730, 'HP:0031528', 'Subretinal deposits', 'XPO:0130539', 'increased size of the ciliary body', 0.4117647058823529, 6.887869297006056, 1.6840966347682629, 'HP:0012372', 'Abnormal eye morphology'),
(369731, 'HP:0031528', 'Subretinal deposits', 'XPO:0140797', 'abnormally necrotic bipolar neuron', 0.45263157894736844, 8.040873045973026, 1.9077612698957138, 'HP:0000479', 'Abnormal retinal morphology'),
(369732, 'HP:0031528', 'Subretinal deposits', 'XPO:0102411', 'abnormal optic choroid vascular plexus morphology', 0.42045454545454547, 7.796308075334707, 1.8105228990649238, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(369733, 'HP:0031528', 'Subretinal deposits', 'XPO:0102851', 'abnormal retinal rod cell morphology', 0.4942528735632184, 8.040873045973026, 1.9935457378573478, 'HP:0000479', 'Abnormal retinal morphology'),
(369734, 'HP:0031528', 'Subretinal deposits', 'XPO:0141638', 'neoplastic eye', 0.4861111111111111, 6.887869297006056, 1.8298278053291577, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(369735, 'HP:0031528', 'Subretinal deposits', 'XPO:0130079', 'increased size of the olfactory pit', 0.417910447761194, 5.788671267106304, 1.5553604730668558, 'UPHENO:0087472', 'abnormal face morphology'),
(369736, 'HP:0031528', 'Subretinal deposits', 'XPO:0129580', 'increased size of the inner limiting membrane', 0.4777777777777778, 8.040873045973026, 1.960038381077836, 'HP:0000479', 'Abnormal retinal morphology'),
(369737, 'HP:0031528', 'Subretinal deposits', 'XPO:0129083', 'decreased size of the bipolar neuron', 0.4174757281553398, 8.040873045973026, 1.8321761186829812, 'HP:0000479', 'Abnormal retinal morphology'),
(369738, 'HP:0031528', 'Subretinal deposits', 'XPO:0103336', 'decreased size of the eye', 0.4375, 6.887869297006056, 1.7359270772241988, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(369739, 'HP:0031528', 'Subretinal deposits', 'XPO:0100710', 'abnormal hyaloid vein', 0.4626865671641791, 6.887869297006056, 1.7851959556606887, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(369740, 'HP:0031528', 'Subretinal deposits', 'XPO:0141181', 'abnormally necrotic choroid', 0.41333333333333333, 6.575878401988876, 1.6486448190828538, 'UPHENO:0087924', 'abnormal camera-type eye morphology'),
(369741, 'HP:0031528', 'Subretinal deposits', 'XPO:0128491', 'decreased size of the retinal ganglion cell', 0.42574257425742573, 8.040873045973026, 1.850227550835222, 'HP:0000479', 'Abnormal retinal morphology'),
(369742, 'HP:0031528', 'Subretinal deposits', 'XPO:0129432', 'decreased size of the retinal stem cell', 0.4574468085106383, 8.040873045973026, 1.9178820903589395, 'HP:0000479', 'Abnormal retinal morphology'),
(369743, 'HP:0031528', 'Subretinal deposits', 'XPO:0130353', 'increased size of the photoreceptor layer', 0.48314606741573035, 8.040873045973026, 1.9710190741722953, 'HP:0000479', 'Abnormal retinal morphology'),
(369744, 'HP:0031528', 'Subretinal deposits', 'XPO:0128643', 'decreased size of the retinal layer', 0.589041095890411, 8.040873045973026, 2.1763282544036455, 'HP:0000479', 'Abnormal retinal morphology'),
(369745, 'HP:0031528', 'Subretinal deposits', 'XPO:0140808', 'abnormally necrotic retinal cone cell', 0.4673913043478261, 8.040873045973026, 1.938616553383523, 'HP:0000479', 'Abnormal retinal morphology'),
(369746, 'HP:0031528', 'Subretinal deposits', 'XPO:0130048', 'increased size of the optic disc', 0.43661971830985913, 6.575878401988876, 1.6944492248268372, 'UPHENO:0087924', 'abnormal camera-type eye morphology'),
(369747, 'HP:0031528', 'Subretinal deposits', 'XPO:0103022', 'abnormal ciliary body morphology', 0.45454545454545453, 6.887869297006056, 1.769420718895678, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(369748, 'HP:0031528', 'Subretinal deposits', 'XPO:0125909', 'absent retinal blood vessel', 0.524390243902439, 8.040873045973026, 2.053425279323877, 'HP:0000479', 'Abnormal retinal morphology'),
(369749, 'HP:0031528', 'Subretinal deposits', 'XPO:0128787', 'decreased size of the peripheral retina', 0.5443037974683544, 8.040873045973026, 2.0920510830006163, 'HP:0000479', 'Abnormal retinal morphology'),
(369750, 'HP:0031528', 'Subretinal deposits', 'XPO:0140671', 'abnormally necrotic retinal ganglion cell', 0.46236559139784944, 8.040873045973026, 1.9281657141584967, 'HP:0000479', 'Abnormal retinal morphology'),
(369751, 'HP:0031528', 'Subretinal deposits', 'XPO:0128807', 'decreased size of the lens transitional zone', 0.4268292682926829, 6.887869297006056, 1.714626551799759, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(369752, 'HP:0031528', 'Subretinal deposits', 'XPO:0140538', 'abnormally necrotic optic disc', 0.4492753623188406, 6.575878401988876, 1.7188310421964663, 'UPHENO:0087924', 'abnormal camera-type eye morphology'),
(369753, 'HP:0031528', 'Subretinal deposits', 'XPO:0140439', 'abnormally necrotic retinal stem cell', 0.5, 8.040873045973026, 2.0051026215599324, 'HP:0000479', 'Abnormal retinal morphology'),
(369754, 'HP:0031528', 'Subretinal deposits', 'XPO:0130396', 'increased size of the choroid', 0.4025974025974026, 6.575878401988876, 1.627092979653308, 'UPHENO:0087924', 'abnormal camera-type eye morphology'),
(369755, 'HP:0031528', 'Subretinal deposits', 'XPO:0140006', 'abnormally necrotic retinal neural layer', 0.48314606741573035, 8.040873045973026, 1.9710190741722953, 'HP:0000479', 'Abnormal retinal morphology'),
(369756, 'HP:0031528', 'Subretinal deposits', 'XPO:0130906', 'increased size of the retinal stem cell', 0.4574468085106383, 8.040873045973026, 1.9178820903589395, 'HP:0000479', 'Abnormal retinal morphology'),
(369757, 'HP:0031528', 'Subretinal deposits', 'XPO:0102550', 'abnormal lens morphology', 0.4794520547945205, 6.887869297006056, 1.81725152018251, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(369758, 'HP:0031528', 'Subretinal deposits', 'XPO:0140620', 'abnormally necrotic horizontal cell', 0.4725274725274725, 8.040873045973026, 1.9492391893577128, 'HP:0000479', 'Abnormal retinal morphology'),
(369759, 'HP:0031528', 'Subretinal deposits', 'XPO:0128884', 'decreased size of the retinal pigmented epithelium', 0.4725274725274725, 8.040873045973026, 1.9492391893577128, 'HP:0000479', 'Abnormal retinal morphology'),
(369760, 'HP:0031528', 'Subretinal deposits', 'XPO:0140491', 'abnormally necrotic retinal rod cell', 0.4673913043478261, 8.040873045973026, 1.938616553383523, 'HP:0000479', 'Abnormal retinal morphology'),
(369761, 'HP:0031528', 'Subretinal deposits', 'XPO:0102450', 'abnormal retinal stem cell morphology', 0.5308641975308642, 8.040873045973026, 2.066061861851679, 'HP:0000479', 'Abnormal retinal morphology'),
(369762, 'HP:0031528', 'Subretinal deposits', 'XPO:0102831', 'abnormal optic disc morphology', 0.4696969696969697, 6.575878401988876, 1.757461282222151, 'UPHENO:0087924', 'abnormal camera-type eye morphology'),
(369763, 'HP:0031528', 'Subretinal deposits', 'XPO:0140948', 'abnormally necrotic retinal inner nuclear layer', 0.48314606741573035, 8.040873045973026, 1.9710190741722953, 'HP:0000479', 'Abnormal retinal morphology'),
(369764, 'HP:0031528', 'Subretinal deposits', 'XPO:0140593', 'abnormally necrotic Jacobsons organ', 0.4057971014492754, 5.788671267106304, 1.532653261972336, 'UPHENO:0087472', 'abnormal face morphology'),
(369765, 'HP:0031528', 'Subretinal deposits', 'XPO:0102232', 'abnormal eye photoreceptor cell morphology', 0.5058823529411764, 8.040873045973026, 2.0168628550791743, 'HP:0000479', 'Abnormal retinal morphology'),
(369766, 'HP:0031528', 'Subretinal deposits', 'XPO:0102784', 'abnormal retinal progenitor cell region morphology', 0.5972222222222222, 8.040873045973026, 2.191389529299339, 'HP:0000479', 'Abnormal retinal morphology'),
(369767, 'HP:0032721', 'Focal motor seizure with paresis/paralysis', 'XPO:0100032', 'abnormal nervous system', 0.4482758620689655, 3.94131651835137, 1.3292091859262085, 'UPHENO:0004523', 'abnormal nervous system'),
(369768, 'HP:0032721', 'Focal motor seizure with paresis/paralysis', 'XPO:0100274', 'abnormal sensory system', 0.43333333333333335, 3.94131651835137, 1.3068679445984308, 'UPHENO:0004523', 'abnormal nervous system'),
(369769, 'HP:0032721', 'Focal motor seizure with paresis/paralysis', 'XPO:0100642', 'abnormal gustatory system', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(369770, 'HP:0032721', 'Focal motor seizure with paresis/paralysis', 'XPO:0142051', 'abnormal cerebrospinal fluid', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(369771, 'HP:0032721', 'Focal motor seizure with paresis/paralysis', 'XPO:0100164', 'abnormal neural nucleus', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(369772, 'HP:0032721', 'Focal motor seizure with paresis/paralysis', 'XPO:0107253', 'abnormal enteric nervous system', 0.43333333333333335, 3.94131651835137, 1.3068679445984308, 'UPHENO:0004523', 'abnormal nervous system'),
(369773, 'HP:0032721', 'Focal motor seizure with paresis/paralysis', 'XPO:0100427', 'abnormal olfactory system', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(369774, 'HP:0032721', 'Focal motor seizure with paresis/paralysis', 'XPO:0100587', 'abnormal vestibuloauditory system', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(369775, 'HP:0032721', 'Focal motor seizure with paresis/paralysis', 'XPO:0100114', 'abnormal peripheral nervous system', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(369776, 'HP:0032721', 'Focal motor seizure with paresis/paralysis', 'XPO:0100273', 'abnormal visual system', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(369777, 'HP:0032721', 'Focal motor seizure with paresis/paralysis', 'XPO:0100031', 'abnormal central nervous system', 0.43333333333333335, 3.94131651835137, 1.3068679445984308, 'UPHENO:0004523', 'abnormal nervous system'),
(369778, 'HP:0025143', 'Chills', 'XPO:0100006', 'abnormal anatomical structure', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(369779, 'HP:0025143', 'Chills', 'XPO:0101575', 'abnormal vitelline membrane', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(369780, 'HP:0025143', 'Chills', 'XPO:0131470', 'abnormal heart contraction', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(369781, 'HP:0025143', 'Chills', 'XPO:0103783', 'absent hatching behavior', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(369782, 'HP:0025143', 'Chills', 'XPO:0131705', 'abnormal chemotaxis', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(369783, 'HP:0025143', 'Chills', 'XPO:0101110', 'abnormal cell-free extract', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(369784, 'HP:0025143', 'Chills', 'XPO:0100674', 'abnormal secondary oogonium', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(369785, 'HP:0025143', 'Chills', 'XPO:0100026', 'abnormal germ cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(369786, 'HP:0025143', 'Chills', 'XPO:0100164', 'abnormal neural nucleus', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(369787, 'HP:0025143', 'Chills', 'XPO:0100437', 'abnormal proepicardium', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(369788, 'HP:0025143', 'Chills', 'XPO:0100691', 'abnormal keratin accumulating cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(369789, 'HP:0025143', 'Chills', 'XPO:0101176', 'abnormal non-ciliated epithelial cell', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(369790, 'HP:0025143', 'Chills', 'XPO:0100394', 'abnormal marginal zone', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(369791, 'HP:0025143', 'Chills', 'XPO:0100465', 'abnormal skeletal system', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(369792, 'HP:0025143', 'Chills', 'XPO:0100626', 'abnormal primordial germ cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(369793, 'HP:0025143', 'Chills', 'XPO:0131730', 'abnormal regulation of protein folding', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(369794, 'HP:0025143', 'Chills', 'XPO:0115509', 'abnormally semi-viable whole organism', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(369795, 'HP:0025143', 'Chills', 'XPO:0101136', 'abnormal ooplasm', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(369796, 'HP:0025143', 'Chills', 'XPO:0107259', 'abnormal animal-vegetal axis', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(369797, 'HP:0025143', 'Chills', 'XPO:0131740', 'abnormal detection of nodal flow', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(369798, 'HP:0025143', 'Chills', 'XPO:0101220', 'abnormal centriole', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(369799, 'HP:0025143', 'Chills', 'XPO:0100802', 'abnormal exocrine cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(369800, 'HP:0025143', 'Chills', 'XPO:0107264', 'abnormal anterior side', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(369801, 'HP:0025143', 'Chills', 'XPO:0100533', 'abnormal melanoblast', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(369802, 'HP:0025143', 'Chills', 'XPO:0101535', 'abnormal absorptive cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(369803, 'HP:0025143', 'Chills', 'XPO:0141968', 'absent cilium motility in ciliated cell', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(369804, 'HP:0025143', 'Chills', 'XPO:0100069', 'abnormal urinary system', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(369805, 'HP:0025143', 'Chills', 'XPO:0107312', 'abnormal filopodium', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(369806, 'HP:0025143', 'Chills', 'XPO:0141315', 'abnormal anatomical region', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(369807, 'HP:0025143', 'Chills', 'XPO:0101283', 'abnormal left-ventral blastomere', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(369808, 'HP:0025143', 'Chills', 'XPO:0141789', 'abnormal hormone catabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(369809, 'HP:0025143', 'Chills', 'XPO:0100186', 'abnormal uveal tract', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(369810, 'HP:0025143', 'Chills', 'XPO:0131738', 'abnormal Wnt signaling pathway', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(369811, 'HP:0025143', 'Chills', 'XPO:0100251', 'abnormal proteinaceous extracellular matrix', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(369812, 'HP:0025143', 'Chills', 'XPO:0131479', 'absent social behavior', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(369813, 'HP:0025143', 'Chills', 'XPO:0107339', 'abnormal yolk platelet', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(369814, 'HP:0025143', 'Chills', 'XPO:0101411', 'abnormal marginal zone (sensu neural)', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(369815, 'HP:0025143', 'Chills', 'XPO:0101333', 'abnormal barrier epithelial cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(369816, 'HP:0025143', 'Chills', 'XPO:0100239', 'abnormal acellular anatomical structure', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(369817, 'HP:0025143', 'Chills', 'XPO:0107268', 'abnormal left side', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(369818, 'HP:0025143', 'Chills', 'XPO:0141892', 'abnormal inositol metabolic process', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(369819, 'HP:0025143', 'Chills', 'XPO:0100308', 'abnormal early embryonic cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(369820, 'HP:0025143', 'Chills', 'XPO:0107284', 'abnormal migrating myoblast', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(369821, 'HP:0025143', 'Chills', 'XPO:0100289', 'abnormal chondroblast', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(369822, 'HP:0025143', 'Chills', 'XPO:0100339', 'abnormal circumblastoporal collar', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(369823, 'HP:0025143', 'Chills', 'XPO:0100894', 'abnormal nucleus', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(369824, 'HP:0025143', 'Chills', 'XPO:0101228', 'abnormal mesenchymal stem cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(369825, 'HP:0025143', 'Chills', 'XPO:0101480', 'abnormal stage V oocyte', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(369826, 'HP:0025143', 'Chills', 'XPO:0131481', 'absent feeding behavior', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(369827, 'HP:0025143', 'Chills', 'XPO:0131729', 'abnormal regulation of growth rate', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(369828, 'HP:0025143', 'Chills', 'XPO:0141264', 'abnormal schooling behavior', 0.5714285714285714, 1.4755025719078136, 0.918228907628411, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(369829, 'HP:0025143', 'Chills', 'XPO:0115391', 'abnormally undifferentiated alimentary system', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(369830, 'HP:0025143', 'Chills', 'XPO:0101078', 'abnormal mucous gland', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(369831, 'HP:0025143', 'Chills', 'XPO:0100427', 'abnormal olfactory system', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(369832, 'HP:0025143', 'Chills', 'XPO:0101378', 'abnormal blastomere D1', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(369833, 'HP:0025143', 'Chills', 'XPO:0100581', 'abnormal immune system', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(369834, 'HP:0025143', 'Chills', 'XPO:0141499', 'abnormal tadpole', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(369835, 'HP:0025143', 'Chills', 'XPO:0100842', 'abnormal left-dorsal blastomere', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(369836, 'HP:0025143', 'Chills', 'XPO:0131719', 'abnormal activation of meiosis', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(369837, 'HP:0025143', 'Chills', 'XPO:0131725', 'abnormal phosphorylation of RNA polymerase II C-terminal domain', 0.5714285714285714, 1.4755025719078136, 0.918228907628411, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(369838, 'HP:0025143', 'Chills', 'XPO:0141781', 'abnormal secondary metabolic process', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(369839, 'HP:0025143', 'Chills', 'XPO:0142056', 'abnormal main body axis', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(369840, 'HP:0025143', 'Chills', 'XPO:0100032', 'abnormal nervous system', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(369841, 'HP:0025143', 'Chills', 'XPO:0141775', 'abnormal nitrogen compound metabolic process', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(369842, 'HP:0025143', 'Chills', 'XPO:0100599', 'abnormal adult immune system', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(369843, 'HP:0025143', 'Chills', 'XPO:0101157', 'abnormal female organism', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(369844, 'HP:0025143', 'Chills', 'XPO:0131722', 'abnormal determination of left/right symmetry', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(369845, 'HP:0025143', 'Chills', 'XPO:0141770', 'abnormal urate homeostasis', 0.5714285714285714, 1.4755025719078136, 0.918228907628411, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(369846, 'HP:0025143', 'Chills', 'XPO:0141760', 'abnormal multicellular organismal homeostasis', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(369847, 'HP:0025143', 'Chills', 'XPO:0100640', 'abnormal notochordal sheath', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(369848, 'HP:0025143', 'Chills', 'XPO:0101547', 'abnormal lampbrush chromosome', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(369849, 'HP:0025143', 'Chills', 'XPO:0107263', 'abnormal anatomical side', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(369850, 'HP:0025143', 'Chills', 'XPO:0100108', 'abnormal cell part', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(369851, 'HP:0025143', 'Chills', 'XPO:0131691', 'abnormal molecular function', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(369852, 'HP:0025143', 'Chills', 'XPO:0141877', 'abnormal 2-deoxyribose 1-phosphate metabolic process', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(369853, 'HP:0025143', 'Chills', 'XPO:0115505', 'dead whole organism', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(369854, 'HP:0025143', 'Chills', 'XPO:0141810', 'abnormal cyclase activity', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(369855, 'HP:0025143', 'Chills', 'XPO:0101373', 'abnormal oxygen accumulating cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(369856, 'HP:0025143', 'Chills', 'XPO:0101519', 'abnormal hypobranchial placode', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(369857, 'HP:0025143', 'Chills', 'XPO:0101061', 'abnormal plasma membrane', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(369858, 'HP:0025143', 'Chills', 'XPO:0100277', 'abnormal blastocoel', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(369859, 'HP:0025143', 'Chills', 'XPO:0116429', 'abnormal behavior', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(369860, 'HP:0025143', 'Chills', 'XPO:0100317', 'abnormal respiratory system', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(369861, 'HP:0025143', 'Chills', 'XPO:0100429', 'abnormal spermatid', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(369862, 'HP:0025143', 'Chills', 'XPO:0101221', 'abnormal larval immune system', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(369863, 'HP:0025143', 'Chills', 'XPO:0141263', 'abnormal visually guided collision avoidance behavior', 0.5714285714285714, 1.4755025719078136, 0.918228907628411, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(369864, 'HP:0025143', 'Chills', 'XPO:0100151', 'abnormal primordium', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(369865, 'HP:0025143', 'Chills', 'XPO:0107265', 'abnormal posterior side', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(369866, 'HP:0025143', 'Chills', 'XPO:0131474', 'absent behavioral response to pain', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(369867, 'HP:0025143', 'Chills', 'XPO:0101113', 'abnormal stage IV oocyte', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(369868, 'HP:0025143', 'Chills', 'XPO:0141961', 'absent cilium motility in mucociliary epithelium', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(369869, 'HP:0025143', 'Chills', 'XPO:0100913', 'abnormal Brachets cleft', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(369870, 'HP:0025143', 'Chills', 'XPO:0107266', 'abnormal dorsal side', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(369871, 'HP:0025143', 'Chills', 'XPO:0100231', 'abnormal compound organ', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(369872, 'HP:0025143', 'Chills', 'XPO:0141791', 'abnormal primary metabolic process', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(369873, 'HP:0025143', 'Chills', 'XPO:0100293', 'abnormal duct', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(369874, 'HP:0025143', 'Chills', 'XPO:0116433', 'abnormal axis specification', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(369875, 'HP:0025143', 'Chills', 'XPO:0141959', 'absent cilium motility in floor plate', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(369876, 'HP:0025143', 'Chills', 'XPO:0100014', 'abnormal tissue', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(369877, 'HP:0025143', 'Chills', 'XPO:0101389', 'abnormal wedge region', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(369878, 'HP:0025143', 'Chills', 'XPO:0141767', 'abnormal temperature homeostasis', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(369879, 'HP:0025143', 'Chills', 'XPO:0107285', 'abnormal flexural organ', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(369880, 'HP:0025143', 'Chills', 'XPO:0100295', 'abnormal extracellular matrix', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(369881, 'HP:0025143', 'Chills', 'XPO:0100417', 'abnormal dense regular connective tissue', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(369882, 'HP:0025143', 'Chills', 'XPO:0101264', 'abnormal mitotic spindle', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(369883, 'HP:0025143', 'Chills', 'XPO:0101570', 'abnormal forelimb region', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(369884, 'HP:0025143', 'Chills', 'XPO:0131666', 'abnormal adherens junction', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(369885, 'HP:0025143', 'Chills', 'XPO:0100162', 'abnormal presumptive rhombomere', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(369886, 'HP:0025143', 'Chills', 'XPO:0131469', 'abnormal heart process', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(369887, 'HP:0025143', 'Chills', 'XPO:0101109', 'abnormal egg cell-free extract', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(369888, 'HP:0025143', 'Chills', 'XPO:0100202', 'abnormal embryo', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(369889, 'HP:0025143', 'Chills', 'XPO:0141778', 'abnormal biosynthetic process', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(369890, 'HP:0025143', 'Chills', 'XPO:0141788', 'abnormal hormone biosynthetic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(369891, 'HP:0025143', 'Chills', 'XPO:0141960', 'absent cilium motility in brain', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(369892, 'HP:0025143', 'Chills', 'XPO:0115508', 'abnormally peramorphic growth of whole organism', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(369893, 'HP:0025143', 'Chills', 'XPO:0100573', 'abnormal extraembryonic structure', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(369894, 'HP:0025143', 'Chills', 'XPO:0107288', 'abnormal larval alimentary system', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(369895, 'HP:0025143', 'Chills', 'XPO:0141809', 'abnormal catalytic activity', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(369896, 'HP:0025143', 'Chills', 'XPO:0100852', 'abnormal interdigital region', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(369897, 'HP:0025143', 'Chills', 'XPO:0141718', 'abnormal posterior notochord', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(369898, 'HP:0025143', 'Chills', 'XPO:0115758', 'abnormally decreased mobility of melanoblast', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(369899, 'HP:0025143', 'Chills', 'XPO:0100688', 'abnormal adipose tissue', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(369900, 'HP:0025143', 'Chills', 'XPO:0131669', 'abnormal Roux spot', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(369901, 'HP:0025143', 'Chills', 'XPO:0100481', 'abnormal anatomical line', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(369902, 'HP:0025143', 'Chills', 'XPO:0100114', 'abnormal peripheral nervous system', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(369903, 'HP:0025143', 'Chills', 'XPO:0100807', 'abnormal matrix-based tissue', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(369904, 'HP:0025143', 'Chills', 'XPO:0100477', 'abnormal pericyte', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(369905, 'HP:0025143', 'Chills', 'XPO:0141813', 'abnormal hydrolase activity', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(369906, 'HP:0025143', 'Chills', 'XPO:0100989', 'abnormal right blastomere', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(369907, 'HP:0025143', 'Chills', 'XPO:0100205', 'abnormal limb segment', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(369908, 'HP:0025143', 'Chills', 'XPO:0100218', 'abnormal epithelial cell', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(369909, 'HP:0025143', 'Chills', 'XPO:0100152', 'abnormal alimentary system', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(369910, 'HP:0025143', 'Chills', 'XPO:0100745', 'abnormal anterior lymph sac', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(369911, 'HP:0025143', 'Chills', 'XPO:0100265', 'abnormal sensory epithelial cell', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(369912, 'HP:0025143', 'Chills', 'XPO:0101174', 'abnormal articular system', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(369913, 'HP:0025143', 'Chills', 'XPO:0100742', 'abnormal musculoskeletal system', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(369914, 'HP:0025143', 'Chills', 'XPO:0101072', 'abnormal mitochondrial cloud', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(369915, 'HP:0025143', 'Chills', 'XPO:0100902', 'abnormal spermatocyte', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(369916, 'HP:0025143', 'Chills', 'XPO:0100976', 'abnormal multiciliated cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(369917, 'HP:0025143', 'Chills', 'XPO:0100503', 'abnormal blastomere D2', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(369918, 'HP:0025143', 'Chills', 'XPO:0101498', 'abnormal stage II oocyte', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(369919, 'HP:0025143', 'Chills', 'XPO:0101168', 'abnormal circulating cell', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(369920, 'HP:0025143', 'Chills', 'XPO:0131477', 'absent visual behavior', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(369921, 'HP:0025143', 'Chills', 'XPO:0141880', 'abnormal ethanolamine metabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(369922, 'HP:0025143', 'Chills', 'XPO:0100781', 'abnormal presumptive ectoderm', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(369923, 'HP:0025143', 'Chills', 'XPO:0101503', 'abnormal organ cortex', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(369924, 'HP:0025143', 'Chills', 'XPO:0141860', 'abnormal malate-aspartate shuttle', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(369925, 'HP:0025143', 'Chills', 'XPO:0100610', 'abnormal appendage', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(369926, 'HP:0025143', 'Chills', 'XPO:0141816', 'abnormal ligase activity', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(369927, 'HP:0025143', 'Chills', 'XPO:0100912', 'abnormal trabecula', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(369928, 'HP:0025143', 'Chills', 'XPO:0131476', 'absent mechanosensory behavior', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(369929, 'HP:0025143', 'Chills', 'XPO:0132054', 'abnormal development of portion of organism substance', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(369930, 'HP:0025143', 'Chills', 'XPO:0107271', 'abnormal apical region', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(369931, 'HP:0025143', 'Chills', 'XPO:0107269', 'abnormal right side', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(369932, 'HP:0025143', 'Chills', 'XPO:0101132', 'abnormal apoptotic cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(369933, 'HP:0025143', 'Chills', 'XPO:0131475', 'absent olfactory behavior', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(369934, 'HP:0025143', 'Chills', 'XPO:0100587', 'abnormal vestibuloauditory system', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(369935, 'HP:0025143', 'Chills', 'XPO:0141815', 'abnormal isomerase activity', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(369936, 'HP:0025143', 'Chills', 'XPO:0100084', 'abnormal anatomical group', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(369937, 'HP:0025143', 'Chills', 'XPO:0100337', 'abnormal zygote', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(369938, 'HP:0025143', 'Chills', 'XPO:0141743', 'abnormal chemical homeostasis within a tissue', 0.5714285714285714, 1.4755025719078136, 0.918228907628411, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(369939, 'HP:0025143', 'Chills', 'XPO:0133340', 'abnormal cell adhesion', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(369940, 'HP:0025143', 'Chills', 'XPO:0100728', 'abnormal cell condensation', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(369941, 'HP:0025143', 'Chills', 'XPO:0141748', 'abnormal gas homeostasis', 0.5714285714285714, 1.4755025719078136, 0.918228907628411, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(369942, 'HP:0025143', 'Chills', 'XPO:0100956', 'abnormal centrosome', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(369943, 'HP:0025143', 'Chills', 'XPO:0100458', 'abnormal autopod', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(369944, 'HP:0025143', 'Chills', 'XPO:0100786', 'abnormal presumptive axial mesoderm', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(369945, 'HP:0025143', 'Chills', 'XPO:0141782', 'abnormal methylation', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(369946, 'HP:0025143', 'Chills', 'XPO:0100724', 'abnormal kinetochore', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(369947, 'HP:0025143', 'Chills', 'XPO:0131687', 'abnormal astral microtubule', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(369948, 'HP:0025143', 'Chills', 'XPO:0100888', 'abnormal microtubule', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(369949, 'HP:0025143', 'Chills', 'XPO:0128000', 'absent behavior', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(369950, 'HP:0025143', 'Chills', 'XPO:0100667', 'abnormal vegetal yolk mass', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(369951, 'HP:0025143', 'Chills', 'XPO:0100991', 'abnormal iliac process primordium', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(369952, 'HP:0025143', 'Chills', 'XPO:0141898', 'abnormal maltose metabolic process', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(369953, 'HP:0025143', 'Chills', 'XPO:0141738', 'abnormal carbon dioxide homeostasis', 0.5714285714285714, 1.4755025719078136, 0.918228907628411, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(369954, 'HP:0025143', 'Chills', 'XPO:0100172', 'abnormal stem cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(369955, 'HP:0025143', 'Chills', 'XPO:0100081', 'abnormal anatomical entity in vitro', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(369956, 'HP:0025143', 'Chills', 'XPO:0131700', 'abnormal BMP signaling pathway', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(369957, 'HP:0025143', 'Chills', 'XPO:0101405', 'abnormal ring structure', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(369958, 'HP:0025143', 'Chills', 'XPO:0131703', 'abnormal cell division', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(369959, 'HP:0025143', 'Chills', 'XPO:0142052', 'abnormal nasal region', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(369960, 'HP:0025143', 'Chills', 'XPO:0141964', 'absent cilium motility in olfactory pit', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(369961, 'HP:0025143', 'Chills', 'XPO:0101212', 'abnormal glomeral mesenchyme', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(369962, 'HP:0025143', 'Chills', 'XPO:0131675', 'abnormal spindle microtubule', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(369963, 'HP:0025143', 'Chills', 'XPO:0101513', 'abnormal basal body', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(369964, 'HP:0025143', 'Chills', 'XPO:0100574', 'abnormal gastrula cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(369965, 'HP:0025143', 'Chills', 'XPO:0100547', 'abnormal blastomere V2', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(369966, 'HP:0025143', 'Chills', 'XPO:0100002', 'abnormal head', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(369967, 'HP:0025143', 'Chills', 'XPO:0100915', 'abnormal dermal system', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(369968, 'HP:0025143', 'Chills', 'XPO:0101472', 'abnormal zygote cortex', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(369969, 'HP:0025143', 'Chills', 'XPO:0141817', 'abnormal demethylase activity', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(369970, 'HP:0025143', 'Chills', 'XPO:0100104', 'abnormal embryonic structure', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(369971, 'HP:0025143', 'Chills', 'XPO:0100551', 'abnormal oocyte cortex', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(369972, 'HP:0025143', 'Chills', 'XPO:0141790', 'abnormal cellular metabolic process', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(369973, 'HP:0025143', 'Chills', 'XPO:0100999', 'abnormal serous membrane', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(369974, 'HP:0025143', 'Chills', 'XPO:0100285', 'abnormal progenitor cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(369975, 'HP:0025143', 'Chills', 'XPO:0100585', 'abnormal elastica externa', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(369976, 'HP:0025143', 'Chills', 'XPO:0107253', 'abnormal enteric nervous system', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(369977, 'HP:0025143', 'Chills', 'XPO:0101240', 'abnormal ciliated non-epidermal cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(369978, 'HP:0025143', 'Chills', 'XPO:0131482', 'absent locomotory behavior', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(369979, 'HP:0025143', 'Chills', 'XPO:0100642', 'abnormal gustatory system', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(369980, 'HP:0025143', 'Chills', 'XPO:0141798', 'abnormal lipid metabolic process', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(369981, 'HP:0025143', 'Chills', 'XPO:0100545', 'abnormal male organism', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(369982, 'HP:0025143', 'Chills', 'XPO:0101326', 'abnormal cementoblast', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(369983, 'HP:0025143', 'Chills', 'XPO:0141911', 'abnormal ribose phosphate metabolic process', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(369984, 'HP:0025143', 'Chills', 'XPO:0141276', 'decreased surface breathing', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(369985, 'HP:0025143', 'Chills', 'XPO:0101040', 'abnormal axial mesoderm', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(369986, 'HP:0025143', 'Chills', 'XPO:0107258', 'abnormal anatomical axis', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(369987, 'HP:0025143', 'Chills', 'XPO:0141267', 'abnormal resting posture', 0.5714285714285714, 1.4755025719078136, 0.918228907628411, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(369988, 'HP:0025143', 'Chills', 'XPO:0141266', 'abnormal surface breathing', 0.5714285714285714, 1.4755025719078136, 0.918228907628411, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(369989, 'HP:0025143', 'Chills', 'XPO:0100969', 'abnormal disaggregated/reaggregated ectoderm treated with activin', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(369990, 'HP:0025143', 'Chills', 'XPO:0141965', 'absent cilium motility in alimentary system', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(369991, 'HP:0025143', 'Chills', 'XPO:0101347', 'abnormal hindlimb region', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(369992, 'HP:0025143', 'Chills', 'XPO:0115512', 'abnormally semi-erect whole organism', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(369993, 'HP:0025143', 'Chills', 'XPO:0100762', 'abnormal intersomitic region', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(369994, 'HP:0025143', 'Chills', 'XPO:0101451', 'abnormal dorsal lymph space', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(369995, 'HP:0025143', 'Chills', 'XPO:0101241', 'abnormal nucleate erythrocyte', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(369996, 'HP:0025143', 'Chills', 'XPO:0100004', 'abnormal cell', 0.5263157894736842, 1.8210412618256888, 0.9790009036675816, 'HP:0000118', 'Phenotypic abnormality'),
(369997, 'HP:0025143', 'Chills', 'XPO:00000000', 'Xenopus phenotype', 0.6153846153846154, 1.4755025719078136, 0.9528911704452407, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(369998, 'HP:0025143', 'Chills', 'XPO:0141907', 'abnormal putrescine metabolic process', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(369999, 'HP:0025143', 'Chills', 'XPO:0141745', 'abnormal creatinine homeostasis', 0.5714285714285714, 1.4755025719078136, 0.918228907628411, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(370000, 'HP:0025143', 'Chills', 'XPO:0100268', 'abnormal circulatory system', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(370001, 'HP:0025143', 'Chills', 'XPO:0100549', 'abnormal mitotic cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(370002, 'HP:0025143', 'Chills', 'XPO:0100900', 'abnormal angioblast', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(370003, 'HP:0025143', 'Chills', 'XPO:0141600', 'absent metamorphosis', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(370004, 'HP:0025143', 'Chills', 'XPO:0100546', 'abnormal whole organism', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(370005, 'HP:0025143', 'Chills', 'XPO:0101297', 'abnormal barrier cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(370006, 'HP:0025143', 'Chills', 'XPO:0100386', 'abnormal limb', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(370007, 'HP:0025143', 'Chills', 'XPO:0107276', 'abnormal dorsal region', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(370008, 'HP:0025143', 'Chills', 'XPO:0131685', 'abnormal cortical actin cytoskeleton', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(370009, 'HP:0025143', 'Chills', 'XPO:0100307', 'abnormal blastomere', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(370010, 'HP:0025143', 'Chills', 'XPO:0131667', 'abnormal actin cytoskeleton', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(370011, 'HP:0025143', 'Chills', 'XPO:0100273', 'abnormal visual system', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(370012, 'HP:0025143', 'Chills', 'XPO:0100060', 'abnormal regenerating tissue', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(370013, 'HP:0025143', 'Chills', 'XPO:0100135', 'abnormal surface structure', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(370014, 'HP:0025143', 'Chills', 'XPO:0100653', 'abnormal myoblast', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(370015, 'HP:0025143', 'Chills', 'XPO:0101463', 'abnormal right-ventral blastomere', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(370016, 'HP:0025143', 'Chills', 'XPO:0101302', 'abnormal subcortical cytoplasm', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(370017, 'HP:0025143', 'Chills', 'XPO:0141272', 'absent surface breathing', 0.5714285714285714, 1.4755025719078136, 0.918228907628411, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(370018, 'HP:0025143', 'Chills', 'XPO:0100511', 'abnormal stylopod', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(370019, 'HP:0025143', 'Chills', 'XPO:0141841', 'abnormality of whole organism mass', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(370020, 'HP:0025143', 'Chills', 'XPO:0107273', 'abnormal basal region', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(370021, 'HP:0025143', 'Chills', 'XPO:0100031', 'abnormal central nervous system', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(370022, 'HP:0025143', 'Chills', 'XPO:0141271', 'increased surface breathing', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(370023, 'HP:0025143', 'Chills', 'XPO:0141715', 'abnormal septum', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(370024, 'HP:0025143', 'Chills', 'XPO:0141812', 'abnormal transferase activity', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(370025, 'HP:0025143', 'Chills', 'XPO:0100501', 'abnormal urogenital system', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(370026, 'HP:0025143', 'Chills', 'XPO:0100003', 'abnormal organism subdivision', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(370027, 'HP:0025143', 'Chills', 'XPO:0107270', 'abnormal proximal-distal axis', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(370028, 'HP:0025143', 'Chills', 'XPO:0107260', 'abnormal anterior-posterior axis', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(370029, 'HP:0025143', 'Chills', 'XPO:0100754', 'abnormal electrically active cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(370030, 'HP:0025143', 'Chills', 'XPO:0131760', 'abnormal development of anatomical structure', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(370031, 'HP:0025143', 'Chills', 'XPO:0107272', 'abnormal axial region', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(370032, 'HP:0025143', 'Chills', 'XPO:0100917', 'abnormal stage III oocyte', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(370033, 'HP:0025143', 'Chills', 'XPO:0141787', 'abnormal hormone metabolic process', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(370034, 'HP:0025143', 'Chills', 'XPO:0100225', 'abnormal endocrine system', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(370035, 'HP:0025143', 'Chills', 'XPO:0100192', 'abnormal epithelium', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(370036, 'HP:0025143', 'Chills', 'XPO:0142057', 'abnormal desmosome', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(370037, 'HP:0025143', 'Chills', 'XPO:0100493', 'abnormal liver and biliary system', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(370038, 'HP:0025143', 'Chills', 'XPO:0141792', 'abnormal small molecule metabolic process', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(370039, 'HP:0025143', 'Chills', 'XPO:0101071', 'abnormal endoplasmic reticulum', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(370040, 'HP:0025143', 'Chills', 'XPO:0100856', 'abnormal simple organ', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(370041, 'HP:0025143', 'Chills', 'XPO:0100282', 'abnormal pelvic girdle primordium', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(370042, 'HP:0025143', 'Chills', 'XPO:0100274', 'abnormal sensory system', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(370043, 'HP:0025143', 'Chills', 'XPO:0100721', 'abnormal centromere', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(370044, 'HP:0025143', 'Chills', 'XPO:0141814', 'abnormal lyase activity', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(370045, 'HP:0025143', 'Chills', 'XPO:0141772', 'abnormal water homeostasis', 0.5714285714285714, 1.4755025719078136, 0.918228907628411, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(370046, 'HP:0025143', 'Chills', 'XPO:0101366', 'abnormal morula cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(370047, 'HP:0025143', 'Chills', 'XPO:0100415', 'abnormal secretory epithelial cell', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(370048, 'HP:0025143', 'Chills', 'XPO:0101497', 'abnormal ciliary axoneme', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(370049, 'HP:0025143', 'Chills', 'XPO:0131480', 'absent mating behavior', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(370050, 'HP:0025143', 'Chills', 'XPO:0100384', 'abnormal amputated tissue', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(370051, 'HP:0025143', 'Chills', 'XPO:0100062', 'abnormal anatomical space', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(370052, 'HP:0025143', 'Chills', 'XPO:0100784', 'abnormal left blastomere', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(370053, 'HP:0025143', 'Chills', 'XPO:0100372', 'abnormal hematological system', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(370054, 'HP:0025143', 'Chills', 'XPO:0100120', 'abnormal genital system', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(370055, 'HP:0025143', 'Chills', 'XPO:0141795', 'abnormal glycosylation', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(370056, 'HP:0025143', 'Chills', 'XPO:0100423', 'abnormal process', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(370057, 'HP:0025143', 'Chills', 'XPO:0101406', 'abnormal cleavage furrow', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(370058, 'HP:0025143', 'Chills', 'XPO:0100402', 'abnormal zeugopod', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(370059, 'HP:0025143', 'Chills', 'XPO:0100791', 'abnormal multiciliated cell precursor', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(370060, 'HP:0025143', 'Chills', 'XPO:0100638', 'abnormal polar body', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(370061, 'HP:0025143', 'Chills', 'XPO:0131744', 'abnormal apical constriction', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(370062, 'HP:0025143', 'Chills', 'XPO:0107262', 'abnormal left-right axis', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(370063, 'HP:0025143', 'Chills', 'XPO:0131798', 'abnormal development of anatomical space', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(370064, 'HP:0025143', 'Chills', 'XPO:0101074', 'abnormal germinal vesicle', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(370065, 'HP:0025143', 'Chills', 'XPO:0100023', 'abnormal mesenchyme', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(370066, 'HP:0025143', 'Chills', 'XPO:0141784', 'abnormal cellular hormone metabolic process', 0.5714285714285714, 1.4755025719078136, 0.918228907628411, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(370067, 'HP:0025143', 'Chills', 'XPO:0100515', 'abnormal somatic stem cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(370068, 'HP:0025143', 'Chills', 'XPO:0100416', 'abnormal ligament', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(370069, 'HP:0025143', 'Chills', 'XPO:0141783', 'abnormal collagen metabolic process', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(370070, 'HP:0025143', 'Chills', 'XPO:0141265', 'abnormal escape behavior', 0.5714285714285714, 1.4755025719078136, 0.918228907628411, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(370071, 'HP:0025143', 'Chills', 'XPO:0141786', 'abnormal pigment metabolic process', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(370072, 'HP:0025143', 'Chills', 'XPO:0141963', 'absent cilium motility in pronephric nephrostome', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(370073, 'HP:0025143', 'Chills', 'XPO:0101569', 'abnormal activin-induced ectoderm', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(370074, 'HP:0025143', 'Chills', 'XPO:0100531', 'abnormal proliferative region', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(370075, 'HP:0025143', 'Chills', 'XPO:0141811', 'abnormal oxidoreductase activity', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(370076, 'HP:0025143', 'Chills', 'XPO:0101435', 'abnormal paracrine cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(370077, 'HP:0025143', 'Chills', 'XPO:0100009', 'abnormal multi-tissue structure', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(370078, 'HP:0025143', 'Chills', 'XPO:0101448', 'abnormal myelin accumulating cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(370079, 'HP:0025143', 'Chills', 'XPO:0100363', 'abnormal cardiovascular system', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(370080, 'HP:0025143', 'Chills', 'XPO:0101096', 'abnormal tendon', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(370081, 'HP:0025143', 'Chills', 'XPO:0131721', 'abnormal nodal signaling pathway', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(370082, 'HP:0025143', 'Chills', 'XPO:0101141', 'abnormal Keller explant', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(370083, 'HP:0025143', 'Chills', 'XPO:0100715', 'abnormal ciliated cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(370084, 'HP:0025143', 'Chills', 'XPO:0141777', 'abnormal catabolic process', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(370085, 'HP:0025143', 'Chills', 'XPO:0100422', 'abnormal notochord', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(370086, 'HP:0025143', 'Chills', 'XPO:0100392', 'abnormal cilium', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(370087, 'HP:0025143', 'Chills', 'XPO:0100344', 'abnormal portion of organism substance', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(370088, 'HP:0025143', 'Chills', 'XPO:0131677', 'abnormal actin filament', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(370089, 'HP:0025143', 'Chills', 'XPO:0116494', 'absent biological process', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(370090, 'HP:0025143', 'Chills', 'XPO:0141776', 'abnormal metabolic process', 0.5555555555555556, 1.8210412618256888, 1.005827813247954, 'HP:0000118', 'Phenotypic abnormality'),
(370091, 'HP:0025143', 'Chills', 'XPO:0133388', 'absent insulin receptor signaling pathway', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(370092, 'HP:0025143', 'Chills', 'XPO:0100899', 'abnormal secondary spermatogonium', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(370093, 'HP:0025143', 'Chills', 'XPO:0101362', 'abnormal vegetal cortex', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(370094, 'HP:0025143', 'Chills', 'XPO:0116434', 'abnormal biological process', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(370095, 'HP:0025143', 'Chills', 'XPO:0100028', 'abnormal anatomical cluster', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(370096, 'HP:0025143', 'Chills', 'XPO:0107261', 'abnormal dorsal-ventral axis', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(370097, 'HP:0025143', 'Chills', 'XPO:0131714', 'abnormal establishment of tissue polarity', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(370098, 'HP:0025143', 'Chills', 'XPO:0100823', 'abnormal blood', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(370099, 'HP:0025143', 'Chills', 'XPO:0100176', 'abnormal stage VI oocyte', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(370100, 'HP:0025143', 'Chills', 'XPO:0131975', 'abnormal development of anatomical line', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(370101, 'HP:0025143', 'Chills', 'XPO:0133401', 'absent determination of left/right symmetry in lateral plate mesoderm', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(370102, 'HP:0025143', 'Chills', 'XPO:0103624', 'absent anterior/posterior pattern specification in midgut', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(370103, 'HP:0025143', 'Chills', 'XPO:0141794', 'abnormal prosthetic group metabolic process', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(370104, 'HP:0025143', 'Chills', 'XPO:0100025', 'abnormal oocyte', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(370105, 'HP:0025143', 'Chills', 'XPO:0141871', 'abnormal cadaverine transport', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(370106, 'HP:0025143', 'Chills', 'XPO:0107267', 'abnormal ventral side', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(370107, 'HP:0025143', 'Chills', 'XPO:0141744', 'abnormal chemical homeostasis', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(370108, 'HP:0025143', 'Chills', 'XPO:0101461', 'abnormal sperm entry point', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(370109, 'HP:0025143', 'Chills', 'XPO:0101409', 'abnormal perivitelline space', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(370110, 'HP:0025143', 'Chills', 'XPO:0100665', 'abnormal egg jelly', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(370111, 'HP:0025143', 'Chills', 'XPO:0141754', 'abnormal homeostatic process', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(370112, 'HP:0025143', 'Chills', 'XPO:0141797', 'abnormal hydrogen metabolic process', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(370113, 'HP:0025143', 'Chills', 'XPO:0141771', 'abnormal urea homeostasis', 0.5714285714285714, 1.4755025719078136, 0.918228907628411, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(370114, 'HP:0025143', 'Chills', 'XPO:0131723', 'abnormal pathway-restricted SMAD protein phosphorylation', 0.5714285714285714, 1.4755025719078136, 0.918228907628411, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(370115, 'HP:0025143', 'Chills', 'XPO:0101200', 'abnormal joint region', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(370116, 'HP:0025143', 'Chills', 'XPO:0101004', 'abnormal acid secreting cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(370117, 'HP:0025143', 'Chills', 'XPO:0100887', 'abnormal right-dorsal blastomere', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(370118, 'HP:0025143', 'Chills', 'XPO:0107278', 'abnormal medial region', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(370119, 'HP:0025143', 'Chills', 'XPO:0100232', 'abnormal lymphatic system', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(370120, 'HP:0025143', 'Chills', 'XPO:0100070', 'abnormal anatomical system', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(370121, 'HP:0025143', 'Chills', 'XPO:0131728', 'abnormal regulation of cell size', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(370122, 'HP:0025143', 'Chills', 'XPO:0131715', 'abnormal fibroblast growth factor receptor signaling pathway', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(370123, 'HP:0025143', 'Chills', 'XPO:0101237', 'abnormal mucus secreting cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(370124, 'HP:0025143', 'Chills', 'XPO:0101023', 'abnormal ultimobranchial body', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(370125, 'HP:0025143', 'Chills', 'XPO:0141818', 'abnormal peptidoglycan muralytic activity', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(370126, 'HP:0025143', 'Chills', 'XPO:0141904', 'abnormal glucosamine metabolic process', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(370127, 'HP:0025143', 'Chills', 'XPO:0100377', 'abnormal connective tissue', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(370128, 'HP:0025143', 'Chills', 'XPO:0131472', 'absent vocalization behavior', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(370129, 'HP:0025143', 'Chills', 'XPO:0141958', 'absent cilium motility in left-right organizer', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(370130, 'HP:0025143', 'Chills', 'XPO:0131694', 'abnormal RNA polymerase II activity', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(370131, 'HP:0025143', 'Chills', 'XPO:0131765', 'abnormal development of anatomical region', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(370132, 'HP:0025143', 'Chills', 'XPO:0141962', 'absent cilium motility in pronephric kidney', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(370133, 'HP:0025143', 'Chills', 'XPO:0131745', 'abnormal axis elongation', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(370134, 'HP:0025143', 'Chills', 'XPO:0101467', 'abnormal alkali secreting cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(370135, 'HP:0025143', 'Chills', 'XPO:0101468', 'abnormal stage I oocyte', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(370136, 'HP:0025143', 'Chills', 'XPO:0100010', 'abnormal multicellular anatomical structure', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(370137, 'HP:0025143', 'Chills', 'XPO:0100643', 'abnormal thoracic region', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(370138, 'HP:0025143', 'Chills', 'XPO:0133402', 'absent determination of left/right symmetry in alimentary system', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(370139, 'HP:0025143', 'Chills', 'XPO:0141975', 'abnormal cilium motility', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(370140, 'HP:0025143', 'Chills', 'XPO:0141714', 'abnormal anterior notochord', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(370141, 'HP:0025143', 'Chills', 'XPO:0131711', 'abnormal establishment of cell polarity', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(370142, 'HP:0025143', 'Chills', 'XPO:0100862', 'abnormal blastomere V1', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(370143, 'HP:0025143', 'Chills', 'XPO:0100258', 'abnormal organ part', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(370144, 'HP:0025143', 'Chills', 'XPO:0100907', 'abnormal cytoplasm', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(370145, 'HP:0025143', 'Chills', 'XPO:0100704', 'abnormal Merkel cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(370146, 'HP:0025143', 'Chills', 'XPO:0141796', 'abnormal demethylation', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(370147, 'HP:0025143', 'Chills', 'XPO:0133403', 'abnormal developmental process', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(370148, 'HP:0025143', 'Chills', 'XPO:0142051', 'abnormal cerebrospinal fluid', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(370149, 'HP:0025143', 'Chills', 'XPO:0100557', 'abnormal prime meridian', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(370150, 'HP:0025143', 'Chills', 'XPO:0101311', 'abnormal bottle cell', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(370151, 'HP:0025143', 'Chills', 'XPO:0133397', 'abnormal insulin receptor signaling pathway', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(370152, 'HP:0025143', 'Chills', 'XPO:0141724', 'abnormal prevention of polyspermy', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(370153, 'HP:0007479', 'Congenital nonbullous ichthyosiform erythroderma', 'XPO:0129655', 'increased size of the skin', 0.46296296296296297, 11.09310877090129, 2.26620795714932, 'UPHENO:0081431', 'abnormal skin of body morphology in the independent continuant'),
(370154, 'HP:0007479', 'Congenital nonbullous ichthyosiform erythroderma', 'XPO:0102727', 'abnormal skin seromucous gland morphology', 0.40384615384615385, 7.420886955069779, 1.7311547172139254, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(370155, 'HP:0007479', 'Congenital nonbullous ichthyosiform erythroderma', 'XPO:0129993', 'increased size of the Eberth-Kastschenko layer', 0.42105263157894735, 7.420886955069779, 1.7676492811307372, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(370156, 'HP:0007479', 'Congenital nonbullous ichthyosiform erythroderma', 'XPO:0129582', 'increased size of the portion of organism substance', 0.42105263157894735, 5.972749669260594, 1.585825326448175, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(370157, 'HP:0007479', 'Congenital nonbullous ichthyosiform erythroderma', 'XPO:0130356', 'increased size of the skin gland', 0.43636363636363634, 7.420886955069779, 1.7995013800377375, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(370158, 'HP:0007479', 'Congenital nonbullous ichthyosiform erythroderma', 'XPO:0130281', 'increased size of the dermis', 0.43636363636363634, 7.420886955069779, 1.7995013800377375, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(370159, 'HP:0007479', 'Congenital nonbullous ichthyosiform erythroderma', 'XPO:0128175', 'decreased size of the skin', 0.4107142857142857, 11.09310877090129, 2.1345018728479954, 'UPHENO:0081431', 'abnormal skin of body morphology in the independent continuant'),
(370160, 'HP:0007479', 'Congenital nonbullous ichthyosiform erythroderma', 'XPO:0130126', 'increased size of the stratum compactum', 0.42105263157894735, 7.420886955069779, 1.7676492811307372, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(370161, 'HP:0007479', 'Congenital nonbullous ichthyosiform erythroderma', 'XPO:0130438', 'increased size of the granular gland', 0.41379310344827586, 7.420886955069779, 1.752344670285258, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(370162, 'HP:0007479', 'Congenital nonbullous ichthyosiform erythroderma', 'XPO:0129982', 'increased size of the anatomical line', 0.42105263157894735, 5.972749669260594, 1.585825326448175, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(370163, 'HP:0007479', 'Congenital nonbullous ichthyosiform erythroderma', 'XPO:0102561', 'abnormal dermis morphology', 0.4117647058823529, 7.420886955069779, 1.7480444314835069, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(370164, 'HP:0007479', 'Congenital nonbullous ichthyosiform erythroderma', 'XPO:0102626', 'abnormal granular gland morphology', 0.40384615384615385, 7.420886955069779, 1.7311547172139254, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(370165, 'HP:0007479', 'Congenital nonbullous ichthyosiform erythroderma', 'XPO:0102139', 'abnormal skin morphology', 0.4489795918367347, 11.09310877090129, 2.2317211851303833, 'UPHENO:0081431', 'abnormal skin of body morphology in the independent continuant'),
(370166, 'HP:0007479', 'Congenital nonbullous ichthyosiform erythroderma', 'XPO:0130706', 'increased size of the stratum spongiosum', 0.42105263157894735, 7.420886955069779, 1.7676492811307372, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(370167, 'HP:0007479', 'Congenital nonbullous ichthyosiform erythroderma', 'XPO:0130896', 'increased size of the skin seromucous gland', 0.41379310344827586, 7.420886955069779, 1.752344670285258, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(370168, 'HP:0007479', 'Congenital nonbullous ichthyosiform erythroderma', 'XPO:0129487', 'increased size of the anatomical structure', 0.42105263157894735, 5.972749669260594, 1.585825326448175, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(370169, 'HP:0007479', 'Congenital nonbullous ichthyosiform erythroderma', 'XPO:0102615', 'abnormal skin gland morphology', 0.42, 7.420886955069779, 1.7654383368244009, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(370170, 'HP:0001612', 'Weak cry', 'XPO:0101389', 'abnormal wedge region', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(370171, 'HP:0001612', 'Weak cry', 'XPO:0141860', 'abnormal malate-aspartate shuttle', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(370172, 'HP:0001612', 'Weak cry', 'XPO:0100158', 'abnormal neuromere', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(370173, 'HP:0001612', 'Weak cry', 'XPO:0100754', 'abnormal electrically active cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(370174, 'HP:0001612', 'Weak cry', 'XPO:0101092', 'abnormal dorso-lateral marginal zone', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(370175, 'HP:0001612', 'Weak cry', 'XPO:0100422', 'abnormal notochord', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(370176, 'HP:0001612', 'Weak cry', 'XPO:0100858', 'abnormal presumptive midbrain-hindbrain boundary', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(370177, 'HP:0001612', 'Weak cry', 'XPO:0100070', 'abnormal anatomical system', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(370178, 'HP:0001612', 'Weak cry', 'XPO:0100081', 'abnormal anatomical entity in vitro', 0.5294117647058824, 1.706362323152461, 0.9504568842024205, 'UPHENO:0002536', 'abnormal anatomical entity'),
(370179, 'HP:0001612', 'Weak cry', 'XPO:0101004', 'abnormal acid secreting cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(370180, 'HP:0001612', 'Weak cry', 'XPO:0141743', 'abnormal chemical homeostasis within a tissue', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(370181, 'HP:0001612', 'Weak cry', 'XPO:0141790', 'abnormal cellular metabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(370182, 'HP:0001612', 'Weak cry', 'XPO:0100028', 'abnormal anatomical cluster', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(370183, 'HP:0001612', 'Weak cry', 'XPO:0101347', 'abnormal hindlimb region', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(370184, 'HP:0001612', 'Weak cry', 'XPO:0101078', 'abnormal mucous gland', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(370185, 'HP:0001612', 'Weak cry', 'XPO:0100363', 'abnormal cardiovascular system', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(370186, 'HP:0001612', 'Weak cry', 'XPO:0101157', 'abnormal female organism', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(370187, 'HP:0001612', 'Weak cry', 'XPO:0100827', 'abnormal atypical epithelium', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(370188, 'HP:0001612', 'Weak cry', 'XPO:0100372', 'abnormal hematological system', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(370189, 'HP:0001612', 'Weak cry', 'XPO:0100912', 'abnormal trabecula', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(370190, 'HP:0001612', 'Weak cry', 'XPO:0107339', 'abnormal yolk platelet', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(370191, 'HP:0001612', 'Weak cry', 'XPO:0101132', 'abnormal apoptotic cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(370192, 'HP:0001612', 'Weak cry', 'XPO:0107288', 'abnormal larval alimentary system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(370193, 'HP:0001612', 'Weak cry', 'XPO:0107271', 'abnormal apical region', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(370194, 'HP:0001612', 'Weak cry', 'XPO:0100856', 'abnormal simple organ', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(370195, 'HP:0001612', 'Weak cry', 'XPO:0100511', 'abnormal stylopod', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(370196, 'HP:0001612', 'Weak cry', 'XPO:0107266', 'abnormal dorsal side', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(370197, 'HP:0001612', 'Weak cry', 'XPO:0100581', 'abnormal immune system', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(370198, 'HP:0001612', 'Weak cry', 'XPO:0141771', 'abnormal urea homeostasis', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(370199, 'HP:0001612', 'Weak cry', 'XPO:0100176', 'abnormal stage VI oocyte', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(370200, 'HP:0001612', 'Weak cry', 'XPO:0100999', 'abnormal serous membrane', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(370201, 'HP:0001612', 'Weak cry', 'XPO:0131675', 'abnormal spindle microtubule', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(370202, 'HP:0001612', 'Weak cry', 'XPO:0100823', 'abnormal blood', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(370203, 'HP:0001612', 'Weak cry', 'XPO:0101098', 'abnormal mineralized extracellular matrix', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(370204, 'HP:0001612', 'Weak cry', 'XPO:0101553', 'abnormal dental epithelium', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(370205, 'HP:0001612', 'Weak cry', 'XPO:0101311', 'abnormal bottle cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(370206, 'HP:0001612', 'Weak cry', 'XPO:0101061', 'abnormal plasma membrane', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(370207, 'HP:0001612', 'Weak cry', 'XPO:0100537', 'abnormal medium cavity', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(370208, 'HP:0001612', 'Weak cry', 'XPO:0101638', 'abnormal anatomical structure morphology', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(370209, 'HP:0001612', 'Weak cry', 'XPO:0100545', 'abnormal male organism', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(370210, 'HP:0001612', 'Weak cry', 'XPO:0100104', 'abnormal embryonic structure', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(370211, 'HP:0001612', 'Weak cry', 'XPO:0101451', 'abnormal dorsal lymph space', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(370212, 'HP:0001612', 'Weak cry', 'XPO:0101283', 'abnormal left-ventral blastomere', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(370213, 'HP:0001612', 'Weak cry', 'XPO:0100501', 'abnormal urogenital system', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(370214, 'HP:0001612', 'Weak cry', 'XPO:0100653', 'abnormal myoblast', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(370215, 'HP:0001612', 'Weak cry', 'XPO:0107284', 'abnormal migrating myoblast', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(370216, 'HP:0001612', 'Weak cry', 'XPO:0100888', 'abnormal microtubule', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(370217, 'HP:0001612', 'Weak cry', 'XPO:0100384', 'abnormal amputated tissue', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(370218, 'HP:0001612', 'Weak cry', 'XPO:0100285', 'abnormal progenitor cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(370219, 'HP:0001612', 'Weak cry', 'XPO:0101297', 'abnormal barrier cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(370220, 'HP:0001612', 'Weak cry', 'XPO:0100164', 'abnormal neural nucleus', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(370221, 'HP:0001612', 'Weak cry', 'XPO:0100261', 'abnormal multilaminar epithelium', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(370222, 'HP:0001612', 'Weak cry', 'XPO:0100956', 'abnormal centrosome', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(370223, 'HP:0001612', 'Weak cry', 'XPO:0100103', 'abnormal trunk', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(370224, 'HP:0001612', 'Weak cry', 'XPO:0141497', 'abnormal lymphoblast', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(370225, 'HP:0001612', 'Weak cry', 'XPO:0141770', 'abnormal urate homeostasis', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(370226, 'HP:0001612', 'Weak cry', 'XPO:0100724', 'abnormal kinetochore', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(370227, 'HP:0001612', 'Weak cry', 'XPO:0101302', 'abnormal subcortical cytoplasm', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(370228, 'HP:0001612', 'Weak cry', 'XPO:0141775', 'abnormal nitrogen compound metabolic process', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(370229, 'HP:0001612', 'Weak cry', 'XPO:0101221', 'abnormal larval immune system', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(370230, 'HP:0001612', 'Weak cry', 'XPO:0100378', 'abnormal perichondrium', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(370231, 'HP:0001612', 'Weak cry', 'XPO:0100691', 'abnormal keratin accumulating cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(370232, 'HP:0001612', 'Weak cry', 'XPO:0100509', 'abnormal germ plasm', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(370233, 'HP:0001612', 'Weak cry', 'XPO:0100557', 'abnormal prime meridian', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(370234, 'HP:0001612', 'Weak cry', 'XPO:0107285', 'abnormal flexural organ', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(370235, 'HP:0001612', 'Weak cry', 'XPO:0100151', 'abnormal primordium', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(370236, 'HP:0001612', 'Weak cry', 'XPO:0100289', 'abnormal chondroblast', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(370237, 'HP:0001612', 'Weak cry', 'XPO:0100429', 'abnormal spermatid', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(370238, 'HP:0001612', 'Weak cry', 'XPO:0100605', 'abnormal prechordal plate', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(370239, 'HP:0001612', 'Weak cry', 'XPO:0100135', 'abnormal surface structure', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(370240, 'HP:0001612', 'Weak cry', 'XPO:0115391', 'abnormally undifferentiated alimentary system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(370241, 'HP:0001612', 'Weak cry', 'XPO:0100108', 'abnormal cell part', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(370242, 'HP:0001612', 'Weak cry', 'XPO:0100025', 'abnormal oocyte', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(370243, 'HP:0001612', 'Weak cry', 'XPO:0101560', 'abnormal compound organ component', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(370244, 'HP:0001612', 'Weak cry', 'XPO:0101461', 'abnormal sperm entry point', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(370245, 'HP:0001612', 'Weak cry', 'XPO:0100295', 'abnormal extracellular matrix', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(370246, 'HP:0001612', 'Weak cry', 'XPO:0101535', 'abnormal absorptive cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(370247, 'HP:0001612', 'Weak cry', 'XPO:0100627', 'abnormal pharyngeal region', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(370248, 'HP:0001612', 'Weak cry', 'XPO:0100610', 'abnormal appendage', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(370249, 'HP:0001612', 'Weak cry', 'XPO:0101362', 'abnormal vegetal cortex', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(370250, 'HP:0001612', 'Weak cry', 'XPO:0100026', 'abnormal germ cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(370251, 'HP:0001612', 'Weak cry', 'XPO:0100337', 'abnormal zygote', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(370252, 'HP:0001612', 'Weak cry', 'XPO:0107264', 'abnormal anterior side', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(370253, 'HP:0001612', 'Weak cry', 'XPO:0100273', 'abnormal visual system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(370254, 'HP:0001612', 'Weak cry', 'XPO:0131691', 'abnormal molecular function', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(370255, 'HP:0001612', 'Weak cry', 'XPO:0101547', 'abnormal lampbrush chromosome', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(370256, 'HP:0001612', 'Weak cry', 'XPO:0101497', 'abnormal ciliary axoneme', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(370257, 'HP:0001612', 'Weak cry', 'XPO:0101023', 'abnormal ultimobranchial body', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(370258, 'HP:0001612', 'Weak cry', 'XPO:0100640', 'abnormal notochordal sheath', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(370259, 'HP:0001612', 'Weak cry', 'XPO:0100192', 'abnormal epithelium', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(370260, 'HP:0001612', 'Weak cry', 'XPO:0100574', 'abnormal gastrula cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(370261, 'HP:0001612', 'Weak cry', 'XPO:0101448', 'abnormal myelin accumulating cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(370262, 'HP:0001612', 'Weak cry', 'XPO:0107268', 'abnormal left side', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(370263, 'HP:0001612', 'Weak cry', 'XPO:0101264', 'abnormal mitotic spindle', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(370264, 'HP:0001612', 'Weak cry', 'XPO:0100427', 'abnormal olfactory system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(370265, 'HP:0001612', 'Weak cry', 'XPO:0100900', 'abnormal angioblast', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(370266, 'HP:0001612', 'Weak cry', 'XPO:0101074', 'abnormal germinal vesicle', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(370267, 'HP:0001612', 'Weak cry', 'XPO:0141276', 'decreased surface breathing', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(370268, 'HP:0001612', 'Weak cry', 'XPO:0100546', 'abnormal whole organism', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(370269, 'HP:0001612', 'Weak cry', 'XPO:0100249', 'abnormal avascular GAG-rich matrix', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(370270, 'HP:0001612', 'Weak cry', 'XPO:0100989', 'abnormal right blastomere', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(370271, 'HP:0001612', 'Weak cry', 'XPO:0101976', 'abnormal portion of organism substance morphology', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(370272, 'HP:0001612', 'Weak cry', 'XPO:0141266', 'abnormal surface breathing', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(370273, 'HP:0001612', 'Weak cry', 'XPO:0100207', 'abnormal blastema', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(370274, 'HP:0001612', 'Weak cry', 'XPO:0141783', 'abnormal collagen metabolic process', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(370275, 'HP:0001612', 'Weak cry', 'XPO:0100258', 'abnormal organ part', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(370276, 'HP:0001612', 'Weak cry', 'XPO:0100172', 'abnormal stem cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(370277, 'HP:0001612', 'Weak cry', 'XPO:0101010', 'abnormal dorsal marginal zone', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(370278, 'HP:0001612', 'Weak cry', 'XPO:0100721', 'abnormal centromere', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(370279, 'HP:0001612', 'Weak cry', 'XPO:0101029', 'abnormal right spleen primordium', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(370280, 'HP:0001612', 'Weak cry', 'XPO:0100402', 'abnormal zeugopod', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(370281, 'HP:0001612', 'Weak cry', 'XPO:0101406', 'abnormal cleavage furrow', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(370282, 'HP:0001612', 'Weak cry', 'XPO:0100728', 'abnormal cell condensation', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(370283, 'HP:0001612', 'Weak cry', 'XPO:0131725', 'abnormal phosphorylation of RNA polymerase II C-terminal domain', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(370284, 'HP:0001612', 'Weak cry', 'XPO:0101480', 'abnormal stage V oocyte', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(370285, 'HP:0001612', 'Weak cry', 'XPO:0141787', 'abnormal hormone metabolic process', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(370286, 'HP:0001612', 'Weak cry', 'XPO:0101570', 'abnormal forelimb region', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(370287, 'HP:0001612', 'Weak cry', 'XPO:0141748', 'abnormal gas homeostasis', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(370288, 'HP:0001612', 'Weak cry', 'XPO:0100887', 'abnormal right-dorsal blastomere', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(370289, 'HP:0001612', 'Weak cry', 'XPO:0141778', 'abnormal biosynthetic process', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(370290, 'HP:0001612', 'Weak cry', 'XPO:0100902', 'abnormal spermatocyte', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(370291, 'HP:0001612', 'Weak cry', 'XPO:0101373', 'abnormal oxygen accumulating cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(370292, 'HP:0001612', 'Weak cry', 'XPO:0100916', 'abnormal principal cavity', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(370293, 'HP:0001612', 'Weak cry', 'XPO:0100852', 'abnormal interdigital region', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(370294, 'HP:0001612', 'Weak cry', 'XPO:0100014', 'abnormal tissue', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(370295, 'HP:0001612', 'Weak cry', 'XPO:0100196', 'abnormal neuron', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(370296, 'HP:0001612', 'Weak cry', 'XPO:0100423', 'abnormal process', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(370297, 'HP:0001612', 'Weak cry', 'XPO:0100800', 'abnormal ventral marginal zone', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(370298, 'HP:0001612', 'Weak cry', 'XPO:0107278', 'abnormal medial region', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(370299, 'HP:0001612', 'Weak cry', 'XPO:0100232', 'abnormal lymphatic system', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(370300, 'HP:0001612', 'Weak cry', 'XPO:0100394', 'abnormal marginal zone', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(370301, 'HP:0001612', 'Weak cry', 'XPO:0100465', 'abnormal skeletal system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(370302, 'HP:0001612', 'Weak cry', 'XPO:0100256', 'abnormal paired appendage', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(370303, 'HP:0001612', 'Weak cry', 'XPO:0100449', 'abnormal lymphocyte', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(370304, 'HP:0001612', 'Weak cry', 'XPO:0100742', 'abnormal musculoskeletal system', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(370305, 'HP:0001612', 'Weak cry', 'XPO:0141714', 'abnormal anterior notochord', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(370306, 'HP:0001612', 'Weak cry', 'XPO:0107276', 'abnormal dorsal region', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(370307, 'HP:0001612', 'Weak cry', 'XPO:0101450', 'abnormal myeloid cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(370308, 'HP:0001612', 'Weak cry', 'XPO:0101099', 'abnormal ventro-lateral marginal zone', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(370309, 'HP:0001612', 'Weak cry', 'XPO:0100553', 'abnormal laryngeal muscle primordium', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(370310, 'HP:0001612', 'Weak cry', 'XPO:0101107', 'abnormal erythroid cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(370311, 'HP:0001612', 'Weak cry', 'XPO:0100444', 'abnormal cement gland', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(370312, 'HP:0001612', 'Weak cry', 'XPO:0101228', 'abnormal mesenchymal stem cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(370313, 'HP:0001612', 'Weak cry', 'XPO:0100515', 'abnormal somatic stem cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(370314, 'HP:0001612', 'Weak cry', 'XPO:0141315', 'abnormal anatomical region', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(370315, 'HP:0001612', 'Weak cry', 'XPO:0100309', 'abnormal vegetal hemisphere', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(370316, 'HP:0001612', 'Weak cry', 'XPO:0100846', 'abnormal hindlimb', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(370317, 'HP:0001612', 'Weak cry', 'XPO:0100969', 'abnormal disaggregated/reaggregated ectoderm treated with activin', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(370318, 'HP:0001612', 'Weak cry', 'XPO:0131677', 'abnormal actin filament', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(370319, 'HP:0001612', 'Weak cry', 'XPO:0100807', 'abnormal matrix-based tissue', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(370320, 'HP:0001612', 'Weak cry', 'XPO:0100274', 'abnormal sensory system', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(370321, 'HP:0001612', 'Weak cry', 'XPO:0141265', 'abnormal escape behavior', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(370322, 'HP:0001612', 'Weak cry', 'XPO:0101113', 'abnormal stage IV oocyte', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(370323, 'HP:0001612', 'Weak cry', 'XPO:0101713', 'abnormal anatomical entity in vitro morphology', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(370324, 'HP:0001612', 'Weak cry', 'XPO:0100175', 'abnormal migrating neuroblast', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(370325, 'HP:0001612', 'Weak cry', 'XPO:0100218', 'abnormal epithelial cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(370326, 'HP:0001612', 'Weak cry', 'XPO:0100282', 'abnormal pelvic girdle primordium', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(370327, 'HP:0001612', 'Weak cry', 'XPO:0101168', 'abnormal circulating cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(370328, 'HP:0001612', 'Weak cry', 'XPO:0141263', 'abnormal visually guided collision avoidance behavior', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(370329, 'HP:0001612', 'Weak cry', 'XPO:0141271', 'increased surface breathing', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(370330, 'HP:0001612', 'Weak cry', 'XPO:0107259', 'abnormal animal-vegetal axis', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(370331, 'HP:0001612', 'Weak cry', 'XPO:0101071', 'abnormal endoplasmic reticulum', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(370332, 'HP:0001612', 'Weak cry', 'XPO:0100612', 'abnormal unilaminar epithelium', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(370333, 'HP:0001612', 'Weak cry', 'XPO:0101220', 'abnormal centriole', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(370334, 'HP:0001612', 'Weak cry', 'XPO:0100786', 'abnormal presumptive axial mesoderm', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(370335, 'HP:0001612', 'Weak cry', 'XPO:0100415', 'abnormal secretory epithelial cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(370336, 'HP:0001612', 'Weak cry', 'XPO:0100976', 'abnormal multiciliated cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(370337, 'HP:0001612', 'Weak cry', 'XPO:0101569', 'abnormal activin-induced ectoderm', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(370338, 'HP:0001612', 'Weak cry', 'XPO:0101072', 'abnormal mitochondrial cloud', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(370339, 'HP:0001612', 'Weak cry', 'XPO:0101409', 'abnormal perivitelline space', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(370340, 'HP:0001612', 'Weak cry', 'XPO:0131669', 'abnormal Roux spot', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(370341, 'HP:0001612', 'Weak cry', 'XPO:0100268', 'abnormal circulatory system', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(370342, 'HP:0001612', 'Weak cry', 'XPO:0100503', 'abnormal blastomere D2', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(370343, 'HP:0001612', 'Weak cry', 'XPO:0100162', 'abnormal presumptive rhombomere', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(370344, 'HP:0001612', 'Weak cry', 'XPO:0100688', 'abnormal adipose tissue', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(370345, 'HP:0001612', 'Weak cry', 'XPO:0100894', 'abnormal nucleus', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(370346, 'HP:0001612', 'Weak cry', 'XPO:0101110', 'abnormal cell-free extract', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(370347, 'HP:0001612', 'Weak cry', 'XPO:0142054', 'abnormal digestive tract', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(370348, 'HP:0001612', 'Weak cry', 'XPO:0101149', 'abnormal amputated limb', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(370349, 'HP:0001612', 'Weak cry', 'XPO:0100060', 'abnormal regenerating tissue', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(370350, 'HP:0001612', 'Weak cry', 'XPO:0100551', 'abnormal oocyte cortex', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(370351, 'HP:0001612', 'Weak cry', 'XPO:0101141', 'abnormal Keller explant', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(370352, 'HP:0001612', 'Weak cry', 'XPO:0101109', 'abnormal egg cell-free extract', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(370353, 'HP:0001612', 'Weak cry', 'XPO:0100842', 'abnormal left-dorsal blastomere', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(370354, 'HP:0001612', 'Weak cry', 'XPO:0101176', 'abnormal non-ciliated epithelial cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(370355, 'HP:0001612', 'Weak cry', 'XPO:0107260', 'abnormal anterior-posterior axis', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(370356, 'HP:0001612', 'Weak cry', 'XPO:0100383', 'abnormal amputated fin', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(370357, 'HP:0001612', 'Weak cry', 'XPO:0101136', 'abnormal ooplasm', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(370358, 'HP:0001612', 'Weak cry', 'XPO:0100393', 'abnormal involuting marginal zone', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(370359, 'HP:0001612', 'Weak cry', 'XPO:0101405', 'abnormal ring structure', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(370360, 'HP:0001612', 'Weak cry', 'XPO:0107253', 'abnormal enteric nervous system', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(370361, 'HP:0001612', 'Weak cry', 'XPO:0141499', 'abnormal tadpole', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(370362, 'HP:0001612', 'Weak cry', 'XPO:0141841', 'abnormality of whole organism mass', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(370363, 'HP:0001612', 'Weak cry', 'XPO:0107262', 'abnormal left-right axis', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(370364, 'HP:0001612', 'Weak cry', 'XPO:0142051', 'abnormal cerebrospinal fluid', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(370365, 'HP:0001612', 'Weak cry', 'XPO:0115505', 'dead whole organism', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(370366, 'HP:0001612', 'Weak cry', 'XPO:0100854', 'abnormal spiracle', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(370367, 'HP:0001612', 'Weak cry', 'XPO:0142052', 'abnormal nasal region', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(370368, 'HP:0001612', 'Weak cry', 'XPO:0100481', 'abnormal anatomical line', 0.5294117647058824, 1.706362323152461, 0.9504568842024205, 'UPHENO:0002536', 'abnormal anatomical entity'),
(370369, 'HP:0001612', 'Weak cry', 'XPO:0100202', 'abnormal embryo', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(370370, 'HP:0001612', 'Weak cry', 'XPO:0101519', 'abnormal hypobranchial placode', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(370371, 'HP:0001612', 'Weak cry', 'XPO:0101224', 'abnormal dorsal involuting marginal zone', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(370372, 'HP:0001612', 'Weak cry', 'XPO:0100205', 'abnormal limb segment', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(370373, 'HP:0001612', 'Weak cry', 'XPO:0101240', 'abnormal ciliated non-epidermal cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(370374, 'HP:0001612', 'Weak cry', 'XPO:0100913', 'abnormal Brachets cleft', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(370375, 'HP:0001612', 'Weak cry', 'XPO:0101472', 'abnormal zygote cortex', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(370376, 'HP:0001612', 'Weak cry', 'XPO:0131723', 'abnormal pathway-restricted SMAD protein phosphorylation', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(370377, 'HP:0001612', 'Weak cry', 'XPO:0100573', 'abnormal extraembryonic structure', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(370378, 'HP:0001612', 'Weak cry', 'XPO:0101349', 'abnormal trunk region', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(370379, 'HP:0001612', 'Weak cry', 'XPO:0100707', 'abnormal central vegetal yolk mass', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(370380, 'HP:0001612', 'Weak cry', 'XPO:0141267', 'abnormal resting posture', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(370381, 'HP:0001612', 'Weak cry', 'XPO:0100899', 'abnormal secondary spermatogonium', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(370382, 'HP:0001612', 'Weak cry', 'XPO:0100843', 'abnormal fasciculated network of fibrils', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(370383, 'HP:0001612', 'Weak cry', 'XPO:0141904', 'abnormal glucosamine metabolic process', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(370384, 'HP:0001612', 'Weak cry', 'XPO:0107258', 'abnormal anatomical axis', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(370385, 'HP:0001612', 'Weak cry', 'XPO:0107265', 'abnormal posterior side', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(370386, 'HP:0001612', 'Weak cry', 'XPO:0101212', 'abnormal glomeral mesenchyme', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(370387, 'HP:0001612', 'Weak cry', 'XPO:0100344', 'abnormal portion of organism substance', 0.5294117647058824, 1.706362323152461, 0.9504568842024205, 'UPHENO:0002536', 'abnormal anatomical entity'),
(370388, 'HP:0001612', 'Weak cry', 'XPO:0100599', 'abnormal adult immune system', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(370389, 'HP:0001612', 'Weak cry', 'XPO:0100339', 'abnormal circumblastoporal collar', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(370390, 'HP:0001612', 'Weak cry', 'XPO:0101503', 'abnormal organ cortex', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(370391, 'HP:0001612', 'Weak cry', 'XPO:0141782', 'abnormal methylation', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(370392, 'HP:0001612', 'Weak cry', 'XPO:0100416', 'abnormal ligament', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(370393, 'HP:0001612', 'Weak cry', 'XPO:0101463', 'abnormal right-ventral blastomere', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(370394, 'HP:0001612', 'Weak cry', 'XPO:0107273', 'abnormal basal region', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(370395, 'HP:0001612', 'Weak cry', 'XPO:0100762', 'abnormal intersomitic region', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(370396, 'HP:0001612', 'Weak cry', 'XPO:0131667', 'abnormal actin cytoskeleton', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(370397, 'HP:0001612', 'Weak cry', 'XPO:0101498', 'abnormal stage II oocyte', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(370398, 'HP:0001612', 'Weak cry', 'XPO:0100201', 'abnormal cavitated compound organ', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(370399, 'HP:0001612', 'Weak cry', 'XPO:0100935', 'abnormal skeleton', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(370400, 'HP:0001612', 'Weak cry', 'XPO:0141792', 'abnormal small molecule metabolic process', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(370401, 'HP:0001612', 'Weak cry', 'XPO:0100587', 'abnormal vestibuloauditory system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(370402, 'HP:0001612', 'Weak cry', 'XPO:0102113', 'abnormal anatomical line morphology', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(370403, 'HP:0001612', 'Weak cry', 'XPO:0100114', 'abnormal peripheral nervous system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(370404, 'HP:0001612', 'Weak cry', 'XPO:0115512', 'abnormally semi-erect whole organism', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(370405, 'HP:0001612', 'Weak cry', 'XPO:0107311', 'abnormal apical junction complex', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(370406, 'HP:0001612', 'Weak cry', 'XPO:0141772', 'abnormal water homeostasis', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(370407, 'HP:0001612', 'Weak cry', 'XPO:0100203', 'abnormal endocrine cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(370408, 'HP:0001612', 'Weak cry', 'XPO:0141738', 'abnormal carbon dioxide homeostasis', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(370409, 'HP:0001612', 'Weak cry', 'XPO:0100468', 'abnormal muscular system', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(370410, 'HP:0001612', 'Weak cry', 'XPO:0100531', 'abnormal proliferative region', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(370411, 'HP:0001612', 'Weak cry', 'XPO:0100386', 'abnormal limb', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(370412, 'HP:0001612', 'Weak cry', 'XPO:0100186', 'abnormal uveal tract', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(370413, 'HP:0001612', 'Weak cry', 'XPO:0100392', 'abnormal cilium', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(370414, 'HP:0001612', 'Weak cry', 'XPO:0100031', 'abnormal central nervous system', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(370415, 'HP:0001612', 'Weak cry', 'XPO:0115509', 'abnormally semi-viable whole organism', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(370416, 'HP:0001612', 'Weak cry', 'XPO:0100722', 'abnormal barbel', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(370417, 'HP:0001612', 'Weak cry', 'XPO:0101575', 'abnormal vitelline membrane', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(370418, 'HP:0001612', 'Weak cry', 'XPO:0142056', 'abnormal main body axis', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(370419, 'HP:0001612', 'Weak cry', 'XPO:0101241', 'abnormal nucleate erythrocyte', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(370420, 'HP:0001612', 'Weak cry', 'XPO:0100307', 'abnormal blastomere', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(370421, 'HP:0001612', 'Weak cry', 'XPO:0107312', 'abnormal filopodium', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(370422, 'HP:0001612', 'Weak cry', 'XPO:0100317', 'abnormal respiratory system', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(370423, 'HP:0001612', 'Weak cry', 'XPO:0100585', 'abnormal elastica externa', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(370424, 'HP:0001612', 'Weak cry', 'XPO:0100802', 'abnormal exocrine cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(370425, 'HP:0001612', 'Weak cry', 'XPO:0101200', 'abnormal joint region', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(370426, 'HP:0001612', 'Weak cry', 'XPO:0101467', 'abnormal alkali secreting cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(370427, 'HP:0001612', 'Weak cry', 'XPO:0100477', 'abnormal pericyte', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(370428, 'HP:0001612', 'Weak cry', 'XPO:0100917', 'abnormal stage III oocyte', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(370429, 'HP:0001612', 'Weak cry', 'XPO:0100006', 'abnormal anatomical structure', 0.5294117647058824, 1.706362323152461, 0.9504568842024205, 'UPHENO:0002536', 'abnormal anatomical entity'),
(370430, 'HP:0001612', 'Weak cry', 'XPO:0141796', 'abnormal demethylation', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(370431, 'HP:0001612', 'Weak cry', 'XPO:0101096', 'abnormal tendon', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(370432, 'HP:0001612', 'Weak cry', 'XPO:0141781', 'abnormal secondary metabolic process', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(370433, 'HP:0001612', 'Weak cry', 'XPO:0100702', 'abnormal glial cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(370434, 'HP:0001612', 'Weak cry', 'XPO:0107263', 'abnormal anatomical side', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(370435, 'HP:0001612', 'Weak cry', 'XPO:0100915', 'abnormal dermal system', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(370436, 'HP:0001612', 'Weak cry', 'XPO:0100296', 'abnormal tail region', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(370437, 'HP:0001612', 'Weak cry', 'XPO:0131685', 'abnormal cortical actin cytoskeleton', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(370438, 'HP:0001612', 'Weak cry', 'XPO:0100133', 'abnormal solid compound organ', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(370439, 'HP:0001612', 'Weak cry', 'XPO:0142057', 'abnormal desmosome', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(370440, 'HP:0001612', 'Weak cry', 'XPO:0141794', 'abnormal prosthetic group metabolic process', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(370441, 'HP:0001612', 'Weak cry', 'XPO:0100003', 'abnormal organism subdivision', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(370442, 'HP:0001612', 'Weak cry', 'XPO:0100727', 'abnormal odontogenic papilla', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(370443, 'HP:0001612', 'Weak cry', 'XPO:0101424', 'abnormal coelomic epithelium', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(370444, 'HP:0001612', 'Weak cry', 'XPO:0101366', 'abnormal morula cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(370445, 'HP:0001612', 'Weak cry', 'XPO:0101501', 'abnormal parabrachial area', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(370446, 'HP:0001612', 'Weak cry', 'XPO:0141264', 'abnormal schooling behavior', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(370447, 'HP:0001612', 'Weak cry', 'XPO:0100791', 'abnormal multiciliated cell precursor', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(370448, 'HP:0001612', 'Weak cry', 'XPO:0100643', 'abnormal thoracic region', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(370449, 'HP:0001612', 'Weak cry', 'XPO:0100225', 'abnormal endocrine system', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(370450, 'HP:0001612', 'Weak cry', 'XPO:0101468', 'abnormal stage I oocyte', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(370451, 'HP:0001612', 'Weak cry', 'XPO:0101411', 'abnormal marginal zone (sensu neural)', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(370452, 'HP:0001612', 'Weak cry', 'XPO:0141272', 'absent surface breathing', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(370453, 'HP:0001612', 'Weak cry', 'XPO:0107261', 'abnormal dorsal-ventral axis', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(370454, 'HP:0001612', 'Weak cry', 'XPO:0141791', 'abnormal primary metabolic process', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(370455, 'HP:0001612', 'Weak cry', 'XPO:0100547', 'abnormal blastomere V2', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(370456, 'HP:0001612', 'Weak cry', 'XPO:0101174', 'abnormal articular system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(370457, 'HP:0001612', 'Weak cry', 'XPO:0100667', 'abnormal vegetal yolk mass', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(370458, 'HP:0001612', 'Weak cry', 'XPO:0100588', 'abnormal unicellular gland', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(370459, 'HP:0001612', 'Weak cry', 'XPO:0107267', 'abnormal ventral side', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(370460, 'HP:0001612', 'Weak cry', 'XPO:0100862', 'abnormal blastomere V1', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(370461, 'HP:0001612', 'Weak cry', 'XPO:0101577', 'abnormal notochordal epithelium', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(370462, 'HP:0001612', 'Weak cry', 'XPO:0101333', 'abnormal barrier epithelial cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(370463, 'HP:0001612', 'Weak cry', 'XPO:0100638', 'abnormal polar body', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(370464, 'HP:0001612', 'Weak cry', 'XPO:0131666', 'abnormal adherens junction', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(370465, 'HP:0001612', 'Weak cry', 'XPO:0100493', 'abnormal liver and biliary system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(370466, 'HP:0001612', 'Weak cry', 'XPO:0100890', 'abnormal pharyngeal cavity', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(370467, 'HP:0001612', 'Weak cry', 'XPO:0100458', 'abnormal autopod', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(370468, 'HP:0001612', 'Weak cry', 'XPO:0100484', 'abnormal cement gland primordium', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(370469, 'HP:0001612', 'Weak cry', 'XPO:0131687', 'abnormal astral microtubule', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(370470, 'HP:0001612', 'Weak cry', 'XPO:0141777', 'abnormal catabolic process', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(370471, 'HP:0001612', 'Weak cry', 'XPO:0107269', 'abnormal right side', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(370472, 'HP:0001612', 'Weak cry', 'XPO:0100868', 'abnormal transporting epithelium', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(370473, 'HP:0001612', 'Weak cry', 'XPO:0101543', 'abnormal external gill', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(370474, 'HP:0001612', 'Weak cry', 'XPO:0115758', 'abnormally decreased mobility of melanoblast', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(370475, 'HP:0001612', 'Weak cry', 'XPO:0100796', 'abnormal pseudoblastema', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(370476, 'HP:0001612', 'Weak cry', 'XPO:0100239', 'abnormal acellular anatomical structure', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(370477, 'HP:0001612', 'Weak cry', 'XPO:0101587', 'abnormal hemangioblast', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(370478, 'HP:0001612', 'Weak cry', 'XPO:0107270', 'abnormal proximal-distal axis', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(370479, 'HP:0001612', 'Weak cry', 'XPO:0100265', 'abnormal sensory epithelial cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(370480, 'HP:0001612', 'Weak cry', 'XPO:0141745', 'abnormal creatinine homeostasis', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(370481, 'HP:0001612', 'Weak cry', 'XPO:00000000', 'Xenopus phenotype', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(370482, 'HP:0001612', 'Weak cry', 'XPO:0141797', 'abnormal hydrogen metabolic process', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(370483, 'HP:0001612', 'Weak cry', 'XPO:0100152', 'abnormal alimentary system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(370484, 'HP:0001612', 'Weak cry', 'XPO:0100009', 'abnormal multi-tissue structure', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(370485, 'HP:0001612', 'Weak cry', 'XPO:0100062', 'abnormal anatomical space', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(370486, 'HP:0001612', 'Weak cry', 'XPO:0115508', 'abnormally peramorphic growth of whole organism', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(370487, 'HP:0001612', 'Weak cry', 'XPO:0141715', 'abnormal septum', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(370488, 'HP:0001612', 'Weak cry', 'XPO:0100674', 'abnormal secondary oogonium', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(370489, 'HP:0001612', 'Weak cry', 'XPO:0101237', 'abnormal mucus secreting cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(370490, 'HP:0001612', 'Weak cry', 'XPO:0100277', 'abnormal blastocoel', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(370491, 'HP:0001612', 'Weak cry', 'XPO:0101378', 'abnormal blastomere D1', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(370492, 'HP:0001612', 'Weak cry', 'XPO:0100665', 'abnormal egg jelly', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(370493, 'HP:0001612', 'Weak cry', 'XPO:0100231', 'abnormal compound organ', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(370494, 'HP:0001612', 'Weak cry', 'XPO:0100907', 'abnormal cytoplasm', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(370495, 'HP:0001612', 'Weak cry', 'XPO:0107272', 'abnormal axial region', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(370496, 'HP:0001612', 'Weak cry', 'XPO:0101573', 'abnormal peripheral vegetal yolk mass', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(370497, 'HP:0001612', 'Weak cry', 'XPO:0100032', 'abnormal nervous system', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(370498, 'HP:0001612', 'Weak cry', 'XPO:0116434', 'abnormal biological process', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(370499, 'HP:0001612', 'Weak cry', 'XPO:0100002', 'abnormal head', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(370500, 'HP:0001612', 'Weak cry', 'XPO:0100715', 'abnormal ciliated cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(370501, 'HP:0001612', 'Weak cry', 'XPO:0101326', 'abnormal cementoblast', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(370502, 'HP:0001612', 'Weak cry', 'XPO:0141784', 'abnormal cellular hormone metabolic process', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(370503, 'HP:0001612', 'Weak cry', 'XPO:0100251', 'abnormal proteinaceous extracellular matrix', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(370504, 'HP:0001612', 'Weak cry', 'XPO:0100069', 'abnormal urinary system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(370505, 'HP:0001612', 'Weak cry', 'XPO:0100626', 'abnormal primordial germ cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(370506, 'HP:0001612', 'Weak cry', 'XPO:0100781', 'abnormal presumptive ectoderm', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(370507, 'HP:0001612', 'Weak cry', 'XPO:0100549', 'abnormal mitotic cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(370508, 'HP:0001612', 'Weak cry', 'XPO:0100023', 'abnormal mesenchyme', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(370509, 'HP:0001612', 'Weak cry', 'XPO:0100437', 'abnormal proepicardium', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(370510, 'HP:0001612', 'Weak cry', 'XPO:0100704', 'abnormal Merkel cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(370511, 'HP:0001612', 'Weak cry', 'XPO:0100010', 'abnormal multicellular anatomical structure', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(370512, 'HP:0001612', 'Weak cry', 'XPO:0100642', 'abnormal gustatory system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(370513, 'HP:0001612', 'Weak cry', 'XPO:0100482', 'abnormal Mullerian duct', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(370514, 'HP:0001612', 'Weak cry', 'XPO:0141776', 'abnormal metabolic process', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(370515, 'HP:0001612', 'Weak cry', 'XPO:0100004', 'abnormal cell', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(370516, 'HP:0001612', 'Weak cry', 'XPO:0116494', 'absent biological process', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(370517, 'HP:0001612', 'Weak cry', 'XPO:0100293', 'abnormal duct', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(370518, 'HP:0001612', 'Weak cry', 'XPO:0100991', 'abnormal iliac process primordium', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(370519, 'HP:0001612', 'Weak cry', 'XPO:0100308', 'abnormal early embryonic cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(370520, 'HP:0001612', 'Weak cry', 'XPO:0100377', 'abnormal connective tissue', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(370521, 'HP:0001612', 'Weak cry', 'XPO:0100784', 'abnormal left blastomere', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(370522, 'HP:0001612', 'Weak cry', 'XPO:0101435', 'abnormal paracrine cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(370523, 'HP:0001612', 'Weak cry', 'XPO:0100120', 'abnormal genital system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(370524, 'HP:0001612', 'Weak cry', 'XPO:0100417', 'abnormal dense regular connective tissue', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(370525, 'HP:0001612', 'Weak cry', 'XPO:0100067', 'abnormal animal hemisphere', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(370526, 'HP:0001612', 'Weak cry', 'XPO:0100084', 'abnormal anatomical group', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(370527, 'HP:0001612', 'Weak cry', 'XPO:0101513', 'abnormal basal body', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(370528, 'HP:0001612', 'Weak cry', 'XPO:0101040', 'abnormal axial mesoderm', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(370529, 'HP:0001612', 'Weak cry', 'XPO:0141718', 'abnormal posterior notochord', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(370530, 'HP:0001612', 'Weak cry', 'XPO:0141786', 'abnormal pigment metabolic process', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(370531, 'HP:0001612', 'Weak cry', 'XPO:0100403', 'abnormal forelimb', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(370532, 'HP:0001612', 'Weak cry', 'XPO:0100533', 'abnormal melanoblast', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(370533, 'HP:0001612', 'Weak cry', 'XPO:0100745', 'abnormal anterior lymph sac', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(370534, 'HP:0001612', 'Weak cry', 'XPO:0100816', 'abnormal blastocoel anlage', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(370535, 'HP:0006571', 'Reduced number of intrahepatic bile ducts', 'XPO:0100042', 'abnormal hepatic vein', 0.42857142857142855, 9.184143847054914, 1.9839510197426296, 'UPHENO:0086622', 'abnormal liver morphology'),
(370536, 'HP:0006571', 'Reduced number of intrahepatic bile ducts', 'XPO:0130691', 'increased size of the bile duct', 0.44, 11.042124842182485, 2.2042084589621496, 'UPHENO:0087335', 'abnormal bile duct morphology'),
(370537, 'HP:0006571', 'Reduced number of intrahepatic bile ducts', 'XPO:0130806', 'increased size of the biliary tree', 0.4722222222222222, 11.430690130100139, 2.323322167666273, 'HP:0012440', 'Abnormal biliary tract morphology'),
(370538, 'HP:0006571', 'Reduced number of intrahepatic bile ducts', 'XPO:0102426', 'abnormal liver morphology', 0.4125, 9.184143847054914, 1.9463965004361654, 'UPHENO:0086622', 'abnormal liver morphology'),
(370539, 'HP:0006571', 'Reduced number of intrahepatic bile ducts', 'XPO:0129330', 'decreased size of the biliary tree', 0.4722222222222222, 11.430690130100139, 2.323322167666273, 'HP:0012440', 'Abnormal biliary tract morphology'),
(370540, 'HP:0006571', 'Reduced number of intrahepatic bile ducts', 'XPO:0129215', 'decreased size of the bile duct', 0.44, 11.042124842182485, 2.2042084589621496, 'UPHENO:0087335', 'abnormal bile duct morphology'),
(370541, 'HP:0006571', 'Reduced number of intrahepatic bile ducts', 'XPO:0140388', 'abnormally necrotic biliary tree', 0.4857142857142857, 11.430690130100139, 2.356278738129877, 'HP:0012440', 'Abnormal biliary tract morphology'),
(370542, 'HP:0006571', 'Reduced number of intrahepatic bile ducts', 'XPO:0102763', 'abnormal hepatocyte morphology', 0.4024390243902439, 9.184143847054914, 1.9225134302959865, 'UPHENO:0086622', 'abnormal liver morphology'),
(370543, 'HP:0006571', 'Reduced number of intrahepatic bile ducts', 'XPO:0103168', 'abnormal liver parenchyme morphology', 0.4125, 9.184143847054914, 1.9463965004361654, 'UPHENO:0086622', 'abnormal liver morphology'),
(370544, 'HP:0006571', 'Reduced number of intrahepatic bile ducts', 'XPO:0102825', 'abnormal bile duct morphology', 0.4925373134328358, 11.042124842182485, 2.3320931594510834, 'UPHENO:0087335', 'abnormal bile duct morphology'),
(370545, 'HP:0006571', 'Reduced number of intrahepatic bile ducts', 'XPO:0102211', 'abnormal biliary tree morphology', 0.5230769230769231, 11.430690130100139, 2.4452260063025943, 'HP:0012440', 'Abnormal biliary tract morphology'),
(370546, 'HP:0006571', 'Reduced number of intrahepatic bile ducts', 'XPO:0141005', 'abnormally necrotic bile duct', 0.4520547945205479, 11.042124842182485, 2.2341990682575803, 'UPHENO:0087335', 'abnormal bile duct morphology'),
(370547, 'HP:0008245', 'Pituitary hypothyroidism', 'XPO:0101947', 'abnormal neurohypophysis morphology', 0.41228070175438597, 9.837010412277873, 2.013854402865094, 'UPHENO:0087940', 'abnormal pituitary gland morphology'),
(370548, 'HP:0008245', 'Pituitary hypothyroidism', 'XPO:0102123', 'abnormal pars distalis morphology', 0.40869565217391307, 9.837010412277873, 2.00507939640491, 'UPHENO:0087940', 'abnormal pituitary gland morphology'),
(370549, 'HP:0008245', 'Pituitary hypothyroidism', 'XPO:0102583', 'abnormal adenohypophysis morphology', 0.41228070175438597, 9.837010412277873, 2.013854402865094, 'UPHENO:0087940', 'abnormal pituitary gland morphology'),
(370550, 'HP:0008245', 'Pituitary hypothyroidism', 'XPO:0101865', 'abnormal pars nervosa morphology', 0.40869565217391307, 9.837010412277873, 2.00507939640491, 'UPHENO:0087940', 'abnormal pituitary gland morphology'),
(370551, 'HP:0008245', 'Pituitary hypothyroidism', 'XPO:0102243', 'abnormal hypophysis morphology', 0.415929203539823, 9.837010412277873, 2.0227456355141844, 'UPHENO:0087940', 'abnormal pituitary gland morphology'),
(370552, 'HP:0008245', 'Pituitary hypothyroidism', 'XPO:0102546', 'abnormal pars intermedia morphology', 0.41228070175438597, 9.837010412277873, 2.013854402865094, 'UPHENO:0087940', 'abnormal pituitary gland morphology'),
(370553, 'HP:0034431', 'Joint crepitus', 'XPO:0100882', 'abnormal perichondrial cell', 0.4117647058823529, 4.3395673355180735, 1.3367425584480601, 'UPHENO:0002964', 'abnormal skeletal system'),
(370554, 'HP:0034431', 'Joint crepitus', 'XPO:0102097', 'abnormal skeletal system morphology', 0.40540540540540543, 4.3395673355180735, 1.3263800567483512, 'UPHENO:0002964', 'abnormal skeletal system'),
(370555, 'HP:0034431', 'Joint crepitus', 'XPO:0100973', 'abnormal dermal skeleton', 0.4375, 4.3395673355180735, 1.3778826906849353, 'UPHENO:0002964', 'abnormal skeletal system'),
(370556, 'HP:0034431', 'Joint crepitus', 'XPO:0101174', 'abnormal articular system', 0.4827586206896552, 4.3395673355180735, 1.4473988881039626, 'UPHENO:0002964', 'abnormal skeletal system'),
(370557, 'HP:0034431', 'Joint crepitus', 'XPO:0100228', 'abnormal skeletal subdivision', 0.45161290322580644, 4.3395673355180735, 1.399930213666808, 'UPHENO:0002964', 'abnormal skeletal system'),
(370558, 'HP:0034431', 'Joint crepitus', 'XPO:0100829', 'abnormal postcranial axial skeleton', 0.42424242424242425, 4.3395673355180735, 1.3568450783281876, 'UPHENO:0002964', 'abnormal skeletal system'),
(370559, 'HP:0034431', 'Joint crepitus', 'XPO:0100498', 'abnormal endoskeleton', 0.4375, 4.3395673355180735, 1.3778826906849353, 'UPHENO:0002964', 'abnormal skeletal system'),
(370560, 'HP:0034431', 'Joint crepitus', 'XPO:0100461', 'abnormal craniofacial skeleton', 0.4117647058823529, 4.3395673355180735, 1.3367425584480601, 'UPHENO:0002964', 'abnormal skeletal system'),
(370561, 'HP:0034431', 'Joint crepitus', 'XPO:0100325', 'abnormal axial skeleton', 0.4375, 4.3395673355180735, 1.3778826906849353, 'UPHENO:0002964', 'abnormal skeletal system'),
(370562, 'HP:0034431', 'Joint crepitus', 'XPO:0101586', 'abnormal joint', 0.42424242424242425, 4.3395673355180735, 1.3568450783281876, 'UPHENO:0002964', 'abnormal skeletal system'),
(370563, 'HP:0034431', 'Joint crepitus', 'XPO:0100004', 'abnormal cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(370564, 'HP:0034431', 'Joint crepitus', 'XPO:0100422', 'abnormal notochord', 0.5, 4.3395673355180735, 1.473018556488355, 'UPHENO:0002964', 'abnormal skeletal system'),
(370565, 'HP:0034431', 'Joint crepitus', 'XPO:0141714', 'abnormal anterior notochord', 0.4827586206896552, 4.3395673355180735, 1.4473988881039626, 'UPHENO:0002964', 'abnormal skeletal system'),
(370566, 'HP:0034431', 'Joint crepitus', 'XPO:0125099', 'absent elastica externa', 0.40540540540540543, 4.3395673355180735, 1.3263800567483512, 'UPHENO:0002964', 'abnormal skeletal system'),
(370567, 'HP:0034431', 'Joint crepitus', 'XPO:0100377', 'abnormal connective tissue', 0.41379310344827586, 3.9037819259951223, 1.270967363209146, 'HP:0033127', 'Abnormality of the musculoskeletal system'),
(370568, 'HP:0034431', 'Joint crepitus', 'XPO:0100585', 'abnormal elastica externa', 0.5185185185185185, 4.3395673355180735, 1.5000486744849937, 'UPHENO:0002964', 'abnormal skeletal system'),
(370569, 'HP:0034431', 'Joint crepitus', 'XPO:0100935', 'abnormal skeleton', 0.4666666666666667, 4.3395673355180735, 1.4230711237467255, 'UPHENO:0002964', 'abnormal skeletal system'),
(370570, 'HP:0034431', 'Joint crepitus', 'XPO:0127584', 'abnormally localised articular system', 0.40540540540540543, 4.3395673355180735, 1.3263800567483512, 'UPHENO:0002964', 'abnormal skeletal system'),
(370571, 'HP:0034431', 'Joint crepitus', 'XPO:0100512', 'abnormal cranial skeleton', 0.42424242424242425, 4.3395673355180735, 1.3568450783281876, 'UPHENO:0002964', 'abnormal skeletal system'),
(370572, 'HP:0034431', 'Joint crepitus', 'XPO:0126722', 'abnormally localised elastica externa', 0.4166666666666667, 4.3395673355180735, 1.3446758183539496, 'UPHENO:0002964', 'abnormal skeletal system'),
(370573, 'HP:0034431', 'Joint crepitus', 'XPO:0101484', 'abnormal bone marrow', 0.4117647058823529, 4.3395673355180735, 1.3367425584480601, 'UPHENO:0002964', 'abnormal skeletal system'),
(370574, 'HP:0034431', 'Joint crepitus', 'XPO:0100465', 'abnormal skeletal system', 0.5, 4.3395673355180735, 1.473018556488355, 'UPHENO:0002964', 'abnormal skeletal system'),
(370575, 'HP:0034431', 'Joint crepitus', 'XPO:0100123', 'abnormal pelvic girdle', 0.42424242424242425, 4.3395673355180735, 1.3568450783281876, 'UPHENO:0002964', 'abnormal skeletal system'),
(370576, 'HP:0034431', 'Joint crepitus', 'XPO:0141718', 'abnormal posterior notochord', 0.4827586206896552, 4.3395673355180735, 1.4473988881039626, 'UPHENO:0002964', 'abnormal skeletal system'),
(370577, 'HP:0034431', 'Joint crepitus', 'XPO:0100910', 'abnormal vacuolated notochordal tissue', 0.4375, 4.3395673355180735, 1.3778826906849353, 'UPHENO:0002964', 'abnormal skeletal system'),
(370578, 'HP:0034431', 'Joint crepitus', 'XPO:0100378', 'abnormal perichondrium', 0.4666666666666667, 4.3395673355180735, 1.4230711237467255, 'UPHENO:0002964', 'abnormal skeletal system'),
(370579, 'HP:0034431', 'Joint crepitus', 'XPO:0100350', 'abnormal appendicular skeleton', 0.4375, 4.3395673355180735, 1.3778826906849353, 'UPHENO:0002964', 'abnormal skeletal system'),
(370580, 'HP:0034431', 'Joint crepitus', 'XPO:0100640', 'abnormal notochordal sheath', 0.4827586206896552, 4.3395673355180735, 1.4473988881039626, 'UPHENO:0002964', 'abnormal skeletal system'),
(370581, 'HP:0034431', 'Joint crepitus', 'XPO:0127013', 'abnormally localised skeletal system', 0.4166666666666667, 4.3395673355180735, 1.3446758183539496, 'UPHENO:0002964', 'abnormal skeletal system'),
(370582, 'HP:0034431', 'Joint crepitus', 'XPO:0102217', 'abnormal elastica externa morphology', 0.40540540540540543, 4.3395673355180735, 1.3263800567483512, 'UPHENO:0002964', 'abnormal skeletal system'),
(370583, 'HP:0034431', 'Joint crepitus', 'XPO:0101348', 'abnormal perichordal tissue', 0.4375, 4.3395673355180735, 1.3778826906849353, 'UPHENO:0002964', 'abnormal skeletal system'),
(370584, 'HP:0034431', 'Joint crepitus', 'XPO:0107285', 'abnormal flexural organ', 0.4827586206896552, 4.3395673355180735, 1.4473988881039626, 'UPHENO:0002964', 'abnormal skeletal system'),
(370585, 'HP:0034431', 'Joint crepitus', 'XPO:0125380', 'absent skeletal system', 0.40540540540540543, 4.3395673355180735, 1.3263800567483512, 'UPHENO:0002964', 'abnormal skeletal system'),
(370586, 'HP:0012281', 'Chylous ascites', 'XPO:0130981', 'abnormally increased number of hepato-pancreatic progenitor cell', 0.43478260869565216, 7.050288100320123, 1.7508119979921022, 'UPHENO:0056072', 'abnormally increased number of anatomical entity in the independent continuant'),
(370587, 'HP:0012281', 'Chylous ascites', 'XPO:0124907', 'absent hindgut', 0.4186046511627907, 5.05060299610679, 1.4540309162280658, 'HP:0025031', 'Abnormality of the digestive system'),
(370588, 'HP:0012281', 'Chylous ascites', 'XPO:0141316', 'abnormal anatomical region morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(370589, 'HP:0012281', 'Chylous ascites', 'XPO:0139906', 'abnormally necrotic alimentary system', 0.4318181818181818, 5.05060299610679, 1.476801341705883, 'HP:0025031', 'Abnormality of the digestive system'),
(370590, 'HP:0012281', 'Chylous ascites', 'XPO:0131082', 'abnormally increased number of alkali secreting cell', 0.41025641025641024, 7.050288100320123, 1.7007133466021898, 'UPHENO:0056072', 'abnormally increased number of anatomical entity in the independent continuant'),
(370591, 'HP:0012281', 'Chylous ascites', 'XPO:0102618', 'abnormal gut epithelium morphology', 0.4318181818181818, 5.05060299610679, 1.476801341705883, 'HP:0025031', 'Abnormality of the digestive system'),
(370592, 'HP:0012281', 'Chylous ascites', 'XPO:0128341', 'decreased size of the pharyngeal cavity', 0.4318181818181818, 5.05060299610679, 1.476801341705883, 'HP:0025031', 'Abnormality of the digestive system'),
(370593, 'HP:0012281', 'Chylous ascites', 'XPO:0101713', 'abnormal anatomical entity in vitro morphology', 0.43333333333333335, 2.786899518863159, 1.0989342374200721, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(370594, 'HP:0012281', 'Chylous ascites', 'XPO:0101784', 'abnormal alimentary system morphology', 0.48717948717948717, 5.05060299610679, 1.5686140945403009, 'HP:0025031', 'Abnormality of the digestive system'),
(370595, 'HP:0012281', 'Chylous ascites', 'XPO:0107375', 'abnormal larval alimentary system morphology', 0.4634146341463415, 5.05060299610679, 1.52987690343349, 'HP:0025031', 'Abnormality of the digestive system'),
(370596, 'HP:0012281', 'Chylous ascites', 'XPO:0140185', 'abnormally necrotic manicotto glandulare', 0.40425531914893614, 5.05060299610679, 1.4288922723864537, 'HP:0025031', 'Abnormality of the digestive system'),
(370597, 'HP:0012281', 'Chylous ascites', 'XPO:0131171', 'abnormally increased number of barrier epithelial cell', 0.41025641025641024, 7.050288100320123, 1.7007133466021898, 'UPHENO:0056072', 'abnormally increased number of anatomical entity in the independent continuant'),
(370598, 'HP:0012281', 'Chylous ascites', 'XPO:0140144', 'abnormally necrotic portion of organism substance', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(370599, 'HP:0012281', 'Chylous ascites', 'XPO:0125535', 'absent anterior foregut', 0.4186046511627907, 5.05060299610679, 1.4540309162280658, 'HP:0025031', 'Abnormality of the digestive system'),
(370600, 'HP:0012281', 'Chylous ascites', 'XPO:0124818', 'absent posterior foregut', 0.4186046511627907, 5.05060299610679, 1.4540309162280658, 'HP:0025031', 'Abnormality of the digestive system'),
(370601, 'HP:0012281', 'Chylous ascites', 'XPO:0131061', 'abnormally increased number of keratin accumulating cell', 0.41025641025641024, 7.050288100320123, 1.7007133466021898, 'UPHENO:0056072', 'abnormally increased number of anatomical entity in the independent continuant'),
(370602, 'HP:0012281', 'Chylous ascites', 'XPO:0115391', 'abnormally undifferentiated alimentary system', 0.4411764705882353, 5.05060299610679, 1.4927180591674907, 'HP:0025031', 'Abnormality of the digestive system'),
(370603, 'HP:0012281', 'Chylous ascites', 'XPO:0102113', 'abnormal anatomical line morphology', 0.43333333333333335, 2.786899518863159, 1.0989342374200721, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(370604, 'HP:0012281', 'Chylous ascites', 'XPO:0133441', 'abnormally increased number of cilium in the ciliated cell', 0.43243243243243246, 7.050288100320123, 1.7460736618398618, 'UPHENO:0056072', 'abnormally increased number of anatomical entity in the independent continuant'),
(370605, 'HP:0012281', 'Chylous ascites', 'XPO:0102178', 'abnormal whole organism morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(370606, 'HP:0012281', 'Chylous ascites', 'XPO:0139718', 'abnormally necrotic anatomical structure', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(370607, 'HP:0012281', 'Chylous ascites', 'XPO:0102118', 'abnormal oral evagination morphology', 0.4523809523809524, 5.05060299610679, 1.511554363387861, 'HP:0025031', 'Abnormality of the digestive system'),
(370608, 'HP:0012281', 'Chylous ascites', 'XPO:0140201', 'abnormally necrotic hindgut', 0.40425531914893614, 5.05060299610679, 1.4288922723864537, 'HP:0025031', 'Abnormality of the digestive system'),
(370609, 'HP:0012281', 'Chylous ascites', 'XPO:0101976', 'abnormal portion of organism substance morphology', 0.43333333333333335, 2.786899518863159, 1.0989342374200721, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(370610, 'HP:0012281', 'Chylous ascites', 'XPO:0130986', 'abnormally increased number of germ cell', 0.41025641025641024, 7.050288100320123, 1.7007133466021898, 'UPHENO:0056072', 'abnormally increased number of anatomical entity in the independent continuant'),
(370611, 'HP:0012281', 'Chylous ascites', 'XPO:0140542', 'abnormally necrotic larval alimentary system', 0.40425531914893614, 5.05060299610679, 1.4288922723864537, 'HP:0025031', 'Abnormality of the digestive system'),
(370612, 'HP:0012281', 'Chylous ascites', 'XPO:0142020', 'absent digestive tract', 0.42857142857142855, 5.05060299610679, 1.471238981671103, 'HP:0025031', 'Abnormality of the digestive system'),
(370613, 'HP:0012281', 'Chylous ascites', 'XPO:0131088', 'abnormally increased number of delta cell', 0.40816326530612246, 7.050288100320123, 1.6963692441138989, 'UPHENO:0056072', 'abnormally increased number of anatomical entity in the independent continuant'),
(370614, 'HP:0012281', 'Chylous ascites', 'XPO:0101636', 'abnormal cell morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(370615, 'HP:0012281', 'Chylous ascites', 'XPO:0142034', 'abnormally necrotic digestive tract', 0.41304347826086957, 5.05060299610679, 1.4443402053625447, 'HP:0025031', 'Abnormality of the digestive system'),
(370616, 'HP:0012281', 'Chylous ascites', 'XPO:0131145', 'abnormally increased number of polar body', 0.41025641025641024, 7.050288100320123, 1.7007133466021898, 'UPHENO:0056072', 'abnormally increased number of anatomical entity in the independent continuant'),
(370617, 'HP:0012281', 'Chylous ascites', 'XPO:0100986', 'abnormal gut epithelium', 0.40540540540540543, 5.05060299610679, 1.4309233924911664, 'HP:0025031', 'Abnormality of the digestive system'),
(370618, 'HP:0012281', 'Chylous ascites', 'XPO:0103711', 'increased size of the alimentary system', 0.41304347826086957, 5.05060299610679, 1.4443402053625447, 'HP:0025031', 'Abnormality of the digestive system'),
(370619, 'HP:0012281', 'Chylous ascites', 'XPO:0130973', 'abnormally increased number of stem cell', 0.41025641025641024, 7.050288100320123, 1.7007133466021898, 'UPHENO:0056072', 'abnormally increased number of anatomical entity in the independent continuant'),
(370620, 'HP:0012281', 'Chylous ascites', 'XPO:0102773', 'abnormal Keller explant morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(370621, 'HP:0012281', 'Chylous ascites', 'XPO:0100152', 'abnormal alimentary system', 0.45454545454545453, 5.05060299610679, 1.5151662069205463, 'HP:0025031', 'Abnormality of the digestive system'),
(370622, 'HP:0012281', 'Chylous ascites', 'XPO:0131090', 'abnormally increased number of oxygen accumulating cell', 0.41025641025641024, 7.050288100320123, 1.7007133466021898, 'UPHENO:0056072', 'abnormally increased number of anatomical entity in the independent continuant'),
(370623, 'HP:0012281', 'Chylous ascites', 'XPO:0131130', 'abnormally increased number of myelin accumulating cell', 0.41025641025641024, 7.050288100320123, 1.7007133466021898, 'UPHENO:0056072', 'abnormally increased number of anatomical entity in the independent continuant'),
(370624, 'HP:0012281', 'Chylous ascites', 'XPO:0125214', 'absent midgut', 0.4186046511627907, 5.05060299610679, 1.4540309162280658, 'HP:0025031', 'Abnormality of the digestive system'),
(370625, 'HP:0012281', 'Chylous ascites', 'XPO:0103009', 'abnormal manicotto glandulare morphology', 0.4523809523809524, 5.05060299610679, 1.511554363387861, 'HP:0025031', 'Abnormality of the digestive system'),
(370626, 'HP:0012281', 'Chylous ascites', 'XPO:0101638', 'abnormal anatomical structure morphology', 0.43333333333333335, 2.786899518863159, 1.0989342374200721, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(370627, 'HP:0012281', 'Chylous ascites', 'XPO:0130989', 'abnormally increased number of ciliated cell', 0.41025641025641024, 7.050288100320123, 1.7007133466021898, 'UPHENO:0056072', 'abnormally increased number of anatomical entity in the independent continuant'),
(370628, 'HP:0012281', 'Chylous ascites', 'XPO:0131134', 'abnormally increased number of barrier cell', 0.41025641025641024, 7.050288100320123, 1.7007133466021898, 'UPHENO:0056072', 'abnormally increased number of anatomical entity in the independent continuant'),
(370629, 'HP:0012281', 'Chylous ascites', 'XPO:0102155', 'abnormal midgut morphology', 0.4418604651162791, 5.05060299610679, 1.4938747567910164, 'HP:0025031', 'Abnormality of the digestive system'),
(370630, 'HP:0012281', 'Chylous ascites', 'XPO:0102742', 'abnormal cell-free extract morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(370631, 'HP:0012281', 'Chylous ascites', 'XPO:0140425', 'abnormally necrotic oral evagination', 0.41304347826086957, 5.05060299610679, 1.4443402053625447, 'HP:0025031', 'Abnormality of the digestive system'),
(370632, 'HP:0012281', 'Chylous ascites', 'XPO:0131066', 'abnormally increased number of myoblast', 0.41025641025641024, 7.050288100320123, 1.7007133466021898, 'UPHENO:0056072', 'abnormally increased number of anatomical entity in the independent continuant'),
(370633, 'HP:0012281', 'Chylous ascites', 'XPO:0131039', 'abnormally increased number of digestive enzyme secreting cell', 0.45454545454545453, 7.050288100320123, 1.7901610009260116, 'UPHENO:0056072', 'abnormally increased number of anatomical entity in the independent continuant'),
(370634, 'HP:0012281', 'Chylous ascites', 'XPO:0131165', 'abnormally increased number of cementoblast', 0.41025641025641024, 7.050288100320123, 1.7007133466021898, 'UPHENO:0056072', 'abnormally increased number of anatomical entity in the independent continuant'),
(370635, 'HP:0012281', 'Chylous ascites', 'XPO:0131131', 'abnormally increased number of absorptive cell', 0.41025641025641024, 7.050288100320123, 1.7007133466021898, 'UPHENO:0056072', 'abnormally increased number of anatomical entity in the independent continuant'),
(370636, 'HP:0012281', 'Chylous ascites', 'XPO:0141833', 'edematous alimentary system', 0.4634146341463415, 5.05060299610679, 1.52987690343349, 'HP:0025031', 'Abnormality of the digestive system'),
(370637, 'HP:0012281', 'Chylous ascites', 'XPO:0133445', 'abnormally increased number of cilium in the ciliated non-epidermal cell', 0.41025641025641024, 7.050288100320123, 1.7007133466021898, 'UPHENO:0056072', 'abnormally increased number of anatomical entity in the independent continuant'),
(370638, 'HP:0012281', 'Chylous ascites', 'XPO:0103201', 'abnormal activin-induced ectoderm morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(370639, 'HP:0012281', 'Chylous ascites', 'XPO:0107288', 'abnormal larval alimentary system', 0.4411764705882353, 5.05060299610679, 1.4927180591674907, 'HP:0025031', 'Abnormality of the digestive system'),
(370640, 'HP:0012281', 'Chylous ascites', 'XPO:0131096', 'abnormally increased number of exocrine cell', 0.41025641025641024, 7.050288100320123, 1.7007133466021898, 'UPHENO:0056072', 'abnormally increased number of anatomical entity in the independent continuant'),
(370641, 'HP:0012281', 'Chylous ascites', 'XPO:0101847', 'abnormal first pancreatic bud morphology', 0.40425531914893614, 5.05060299610679, 1.4288922723864537, 'HP:0025031', 'Abnormality of the digestive system'),
(370642, 'HP:0012281', 'Chylous ascites', 'XPO:0131421', 'abnormally increased number of cilium in the alimentary system', 0.4878048780487805, 7.050288100320123, 1.8544985648377907, 'UPHENO:0056072', 'abnormally increased number of anatomical entity in the independent continuant'),
(370643, 'HP:0012281', 'Chylous ascites', 'XPO:0133443', 'abnormally increased number of cilium in the multiciliated cell', 0.41025641025641024, 7.050288100320123, 1.7007133466021898, 'UPHENO:0056072', 'abnormally increased number of anatomical entity in the independent continuant'),
(370644, 'HP:0012281', 'Chylous ascites', 'XPO:0101740', 'abnormal cell part morphology', 0.4166666666666667, 2.786899518863159, 1.0775936770692605, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(370645, 'HP:0012281', 'Chylous ascites', 'XPO:0125084', 'absent larval alimentary system', 0.42857142857142855, 5.05060299610679, 1.471238981671103, 'HP:0025031', 'Abnormality of the digestive system'),
(370646, 'HP:0012281', 'Chylous ascites', 'XPO:0102094', 'abnormal anterior foregut morphology', 0.4318181818181818, 5.05060299610679, 1.476801341705883, 'HP:0025031', 'Abnormality of the digestive system'),
(370647, 'HP:0012281', 'Chylous ascites', 'XPO:0125745', 'absent pharyngeal cavity', 0.45, 5.05060299610679, 1.507571341014433, 'HP:0025031', 'Abnormality of the digestive system'),
(370648, 'HP:0012281', 'Chylous ascites', 'XPO:0103636', 'abnormally increased number of melanoblast', 0.41025641025641024, 7.050288100320123, 1.7007133466021898, 'UPHENO:0056072', 'abnormally increased number of anatomical entity in the independent continuant'),
(370649, 'HP:0012281', 'Chylous ascites', 'XPO:0102801', 'abnormal hepato-pancreatic duct morphology', 0.41304347826086957, 5.05060299610679, 1.4443402053625447, 'HP:0025031', 'Abnormality of the digestive system'),
(370650, 'HP:0012281', 'Chylous ascites', 'XPO:0102522', 'abnormal pharyngeal cavity morphology', 0.48717948717948717, 5.05060299610679, 1.5686140945403009, 'HP:0025031', 'Abnormality of the digestive system'),
(370651, 'HP:0012281', 'Chylous ascites', 'XPO:0126176', 'absent dorsal foregut', 0.4186046511627907, 5.05060299610679, 1.4540309162280658, 'HP:0025031', 'Abnormality of the digestive system'),
(370652, 'HP:0012281', 'Chylous ascites', 'XPO:0140165', 'abnormally necrotic midgut', 0.40425531914893614, 5.05060299610679, 1.4288922723864537, 'HP:0025031', 'Abnormality of the digestive system'),
(370653, 'HP:0012281', 'Chylous ascites', 'XPO:0124857', 'absent alimentary system', 0.45, 5.05060299610679, 1.507571341014433, 'HP:0025031', 'Abnormality of the digestive system'),
(370654, 'HP:0012281', 'Chylous ascites', 'XPO:0102125', 'abnormal liver and biliary system morphology', 0.4634146341463415, 5.05060299610679, 1.52987690343349, 'HP:0025031', 'Abnormality of the digestive system'),
(370655, 'HP:0012281', 'Chylous ascites', 'XPO:0131031', 'abnormally increased number of nucleate erythrocyte', 0.41025641025641024, 7.050288100320123, 1.7007133466021898, 'UPHENO:0056072', 'abnormally increased number of anatomical entity in the independent continuant'),
(370656, 'HP:0012281', 'Chylous ascites', 'XPO:0101377', 'abnormal manicotto glandulare', 0.4166666666666667, 5.05060299610679, 1.45066119926208, 'HP:0025031', 'Abnormality of the digestive system'),
(370657, 'HP:0012281', 'Chylous ascites', 'XPO:0100523', 'abnormal midgut', 0.4166666666666667, 5.05060299610679, 1.45066119926208, 'HP:0025031', 'Abnormality of the digestive system'),
(370658, 'HP:0012281', 'Chylous ascites', 'XPO:0102367', 'abnormal hindgut morphology', 0.4418604651162791, 5.05060299610679, 1.4938747567910164, 'HP:0025031', 'Abnormality of the digestive system'),
(370659, 'HP:0012281', 'Chylous ascites', 'XPO:0126019', 'absent ventral foregut', 0.4186046511627907, 5.05060299610679, 1.4540309162280658, 'HP:0025031', 'Abnormality of the digestive system'),
(370660, 'HP:0012281', 'Chylous ascites', 'XPO:0125663', 'absent oral evagination', 0.42857142857142855, 5.05060299610679, 1.471238981671103, 'HP:0025031', 'Abnormality of the digestive system'),
(370661, 'HP:0012281', 'Chylous ascites', 'XPO:0103233', 'abnormal proctodeum morphology', 0.41304347826086957, 5.05060299610679, 1.4443402053625447, 'HP:0025031', 'Abnormality of the digestive system'),
(370662, 'HP:0012281', 'Chylous ascites', 'XPO:0101694', 'abnormal anatomical space morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(370663, 'HP:0012281', 'Chylous ascites', 'XPO:0130979', 'abnormally increased number of Merkel cell', 0.41025641025641024, 7.050288100320123, 1.7007133466021898, 'UPHENO:0056072', 'abnormally increased number of anatomical entity in the independent continuant'),
(370664, 'HP:0012281', 'Chylous ascites', 'XPO:0101101', 'abnormal posterior foregut', 0.40540540540540543, 5.05060299610679, 1.4309233924911664, 'HP:0025031', 'Abnormality of the digestive system'),
(370665, 'HP:0012281', 'Chylous ascites', 'XPO:0100735', 'abnormal hindgut', 0.4166666666666667, 5.05060299610679, 1.45066119926208, 'HP:0025031', 'Abnormality of the digestive system'),
(370666, 'HP:0012281', 'Chylous ascites', 'XPO:0124888', 'absent liver and biliary system', 0.43902439024390244, 5.05060299610679, 1.4890728325806668, 'HP:0025031', 'Abnormality of the digestive system'),
(370667, 'HP:0012281', 'Chylous ascites', 'XPO:0130964', 'abnormally increased number of cell', 0.43243243243243246, 7.050288100320123, 1.7460736618398618, 'UPHENO:0056072', 'abnormally increased number of anatomical entity in the independent continuant'),
(370668, 'HP:0012281', 'Chylous ascites', 'XPO:0101890', 'abnormal organ part morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(370669, 'HP:0012281', 'Chylous ascites', 'XPO:0107345', 'abnormal anatomical axis morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(370670, 'HP:0012281', 'Chylous ascites', 'XPO:0131136', 'abnormally increased number of multiciliated cell precursor', 0.41025641025641024, 7.050288100320123, 1.7007133466021898, 'UPHENO:0056072', 'abnormally increased number of anatomical entity in the independent continuant'),
(370671, 'HP:0012281', 'Chylous ascites', 'XPO:0100890', 'abnormal pharyngeal cavity', 0.42857142857142855, 5.05060299610679, 1.471238981671103, 'HP:0025031', 'Abnormality of the digestive system'),
(370672, 'HP:0012281', 'Chylous ascites', 'XPO:0102830', 'abnormal digestive enzyme secreting cell morphology', 0.41304347826086957, 5.05060299610679, 1.4443402053625447, 'HP:0025031', 'Abnormality of the digestive system'),
(370673, 'HP:0012281', 'Chylous ascites', 'XPO:0101381', 'abnormal ventral foregut', 0.40540540540540543, 5.05060299610679, 1.4309233924911664, 'HP:0025031', 'Abnormality of the digestive system'),
(370674, 'HP:0012281', 'Chylous ascites', 'XPO:0129821', 'increased size of the pharyngeal cavity', 0.4318181818181818, 5.05060299610679, 1.476801341705883, 'HP:0025031', 'Abnormality of the digestive system'),
(370675, 'HP:0012281', 'Chylous ascites', 'XPO:0100156', 'abnormal foregut', 0.4166666666666667, 5.05060299610679, 1.45066119926208, 'HP:0025031', 'Abnormality of the digestive system'),
(370676, 'HP:0012281', 'Chylous ascites', 'XPO:0142054', 'abnormal digestive tract', 0.42857142857142855, 5.05060299610679, 1.471238981671103, 'HP:0025031', 'Abnormality of the digestive system'),
(370677, 'HP:0012281', 'Chylous ascites', 'XPO:0140114', 'abnormally necrotic liver and biliary system', 0.41304347826086957, 5.05060299610679, 1.4443402053625447, 'HP:0025031', 'Abnormality of the digestive system'),
(370678, 'HP:0012281', 'Chylous ascites', 'XPO:0124991', 'absent foregut', 0.4186046511627907, 5.05060299610679, 1.4540309162280658, 'HP:0025031', 'Abnormality of the digestive system'),
(370679, 'HP:0012281', 'Chylous ascites', 'XPO:0131089', 'abnormally increased number of mitotic cell', 0.41025641025641024, 7.050288100320123, 1.7007133466021898, 'UPHENO:0056072', 'abnormally increased number of anatomical entity in the independent continuant'),
(370680, 'HP:0012281', 'Chylous ascites', 'XPO:0100493', 'abnormal liver and biliary system', 0.4411764705882353, 5.05060299610679, 1.4927180591674907, 'HP:0025031', 'Abnormality of the digestive system'),
(370681, 'HP:0012281', 'Chylous ascites', 'XPO:0102733', 'abnormal posterior foregut morphology', 0.4318181818181818, 5.05060299610679, 1.476801341705883, 'HP:0025031', 'Abnormality of the digestive system'),
(370682, 'HP:0012281', 'Chylous ascites', 'XPO:0139827', 'abnormally necrotic foregut', 0.40425531914893614, 5.05060299610679, 1.4288922723864537, 'HP:0025031', 'Abnormality of the digestive system'),
(370683, 'HP:0012281', 'Chylous ascites', 'XPO:0131129', 'abnormally increased number of chondroblast', 0.41025641025641024, 7.050288100320123, 1.7007133466021898, 'UPHENO:0056072', 'abnormally increased number of anatomical entity in the independent continuant'),
(370684, 'HP:0012281', 'Chylous ascites', 'XPO:0131075', 'abnormally increased number of mucus secreting cell', 0.41025641025641024, 7.050288100320123, 1.7007133466021898, 'UPHENO:0056072', 'abnormally increased number of anatomical entity in the independent continuant'),
(370685, 'HP:0012281', 'Chylous ascites', 'XPO:0142061', 'abnormal digestive tract morphology', 0.4634146341463415, 5.05060299610679, 1.52987690343349, 'HP:0025031', 'Abnormality of the digestive system'),
(370686, 'HP:0012281', 'Chylous ascites', 'XPO:0101788', 'abnormal foregut morphology', 0.4418604651162791, 5.05060299610679, 1.4938747567910164, 'HP:0025031', 'Abnormality of the digestive system'),
(370687, 'HP:0012281', 'Chylous ascites', 'XPO:0103013', 'abnormal ventral foregut morphology', 0.4318181818181818, 5.05060299610679, 1.476801341705883, 'HP:0025031', 'Abnormality of the digestive system'),
(370688, 'HP:0012281', 'Chylous ascites', 'XPO:0130988', 'abnormally increased number of pericyte', 0.41025641025641024, 7.050288100320123, 1.7007133466021898, 'UPHENO:0056072', 'abnormally increased number of anatomical entity in the independent continuant'),
(370689, 'HP:0012281', 'Chylous ascites', 'XPO:0103631', 'abnormally increased number of apoptotic cell', 0.41025641025641024, 7.050288100320123, 1.7007133466021898, 'UPHENO:0056072', 'abnormally increased number of anatomical entity in the independent continuant'),
(370690, 'HP:0012281', 'Chylous ascites', 'XPO:0131110', 'abnormally increased number of paracrine cell', 0.41025641025641024, 7.050288100320123, 1.7007133466021898, 'UPHENO:0056072', 'abnormally increased number of anatomical entity in the independent continuant'),
