(729165, 'HP:0001808', 'Fragile nails', 'XPO:0103409', 'abnormally increased number of claw of hindlimb digit 2 in the regenerating hindlimb', 0.46511627906976744, 10.47734022339896, 2.207528368844969, 'UPHENO:0003071', 'abnormal nail'),
(729166, 'HP:0001808', 'Fragile nails', 'XPO:0129758', 'increased size of the claw of hindlimb digit 4', 0.4117647058823529, 10.47734022339896, 2.0770649762386393, 'UPHENO:0003071', 'abnormal nail'),
(729167, 'HP:0001808', 'Fragile nails', 'XPO:0103618', 'abnormal number of hindlimb digit 5', 0.4027777777777778, 6.393467666143939, 1.6047263626124957, 'HP:0011297', 'Abnormal digit morphology'),
(729168, 'HP:0001808', 'Fragile nails', 'XPO:0103191', 'abnormal claw of hindlimb digit 5 morphology', 0.44680851063829785, 10.47734022339896, 2.1636461773283586, 'UPHENO:0003071', 'abnormal nail'),
(729169, 'HP:0001808', 'Fragile nails', 'XPO:0101810', 'abnormal digit morphology', 0.484375, 6.393467666143939, 1.759782912972072, 'UPHENO:0002905', 'abnormal digit'),
(729170, 'HP:0001808', 'Fragile nails', 'XPO:0140433', 'abnormally necrotic claw of hindlimb digit 4', 0.42, 10.47734022339896, 2.097732798482105, 'UPHENO:0003071', 'abnormal nail'),
(729171, 'HP:0001808', 'Fragile nails', 'XPO:0101869', 'abnormal claw morphology', 0.46153846153846156, 10.47734022339896, 2.1990214841430262, 'UPHENO:0003071', 'abnormal nail'),
(729172, 'HP:0001808', 'Fragile nails', 'XPO:0141208', 'abnormally necrotic digit-joint region', 0.45588235294117646, 6.393467666143939, 1.7072401949037608, 'UPHENO:0002905', 'abnormal digit'),
(729173, 'HP:0001808', 'Fragile nails', 'XPO:0103044', 'abnormal claw of hindlimb digit 4 morphology', 0.44680851063829785, 10.47734022339896, 2.1636461773283586, 'UPHENO:0003071', 'abnormal nail'),
(729174, 'HP:0001808', 'Fragile nails', 'XPO:0125443', 'absent digit-joint region', 0.43283582089552236, 6.393467666143939, 1.6635269236307513, 'UPHENO:0002905', 'abnormal digit'),
(729175, 'HP:0001808', 'Fragile nails', 'XPO:0141218', 'abnormally necrotic claw of hindlimb digit 5', 0.42, 10.47734022339896, 2.097732798482105, 'UPHENO:0003071', 'abnormal nail'),
(729176, 'HP:0001808', 'Fragile nails', 'XPO:0130578', 'increased size of the claw of hindlimb digit 2', 0.4117647058823529, 10.47734022339896, 2.0770649762386393, 'UPHENO:0003071', 'abnormal nail'),
(729177, 'HP:0001808', 'Fragile nails', 'XPO:0127382', 'abnormally localised claw of hindlimb digit 2', 0.49382716049382713, 10.47734022339896, 2.274641767850241, 'UPHENO:0003071', 'abnormal nail'),
(729178, 'HP:0001808', 'Fragile nails', 'XPO:0102880', 'abnormal digit-joint region morphology', 0.484375, 6.393467666143939, 1.759782912972072, 'UPHENO:0002905', 'abnormal digit'),
(729179, 'HP:0001808', 'Fragile nails', 'XPO:0127078', 'abnormally localised digit-joint region', 0.4461538461538462, 6.393467666143939, 1.6889257501472268, 'HP:0011297', 'Abnormal digit morphology'),
(729180, 'HP:0001808', 'Fragile nails', 'XPO:0101244', 'abnormal hindlimb digit 4', 0.4117647058823529, 6.393467666143939, 1.622530225640833, 'UPHENO:0002905', 'abnormal digit'),
(729181, 'HP:0001808', 'Fragile nails', 'XPO:0115773', 'duplicated bone element in claw of hindlimb digit 3', 0.449438202247191, 10.47734022339896, 2.1700039065256567, 'UPHENO:0003071', 'abnormal nail'),
(729182, 'HP:0001808', 'Fragile nails', 'XPO:0101316', 'abnormal hindlimb digit 5', 0.4117647058823529, 6.393467666143939, 1.622530225640833, 'UPHENO:0002905', 'abnormal digit'),
(729183, 'HP:0001808', 'Fragile nails', 'XPO:0100237', 'abnormal claw', 0.5714285714285714, 10.47734022339896, 2.446845225229413, 'UPHENO:0003071', 'abnormal nail'),
(729184, 'HP:0001808', 'Fragile nails', 'XPO:0141535', 'abnormally decreased number of claw in the regenerating hindlimb', 0.45977011494252873, 10.47734022339896, 2.19480475642006, 'UPHENO:0003071', 'abnormal nail'),
(729185, 'HP:0001808', 'Fragile nails', 'XPO:0100825', 'abnormal claw of hindlimb digit 2', 0.5555555555555556, 10.47734022339896, 2.412621928225593, 'UPHENO:0003071', 'abnormal nail'),
(729186, 'HP:0031062', 'Impaired transferring ability', 'XPO:0100728', 'abnormal cell condensation', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(729187, 'HP:0031062', 'Impaired transferring ability', 'XPO:0100014', 'abnormal tissue', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(729188, 'HP:0031062', 'Impaired transferring ability', 'XPO:0131729', 'abnormal regulation of growth rate', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(729189, 'HP:0031062', 'Impaired transferring ability', 'XPO:0131694', 'abnormal RNA polymerase II activity', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(729190, 'HP:0031062', 'Impaired transferring ability', 'XPO:0100386', 'abnormal limb', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(729191, 'HP:0031062', 'Impaired transferring ability', 'XPO:0100004', 'abnormal cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(729192, 'HP:0031062', 'Impaired transferring ability', 'XPO:0141787', 'abnormal hormone metabolic process', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(729193, 'HP:0031062', 'Impaired transferring ability', 'XPO:0131703', 'abnormal cell division', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(729194, 'HP:0031062', 'Impaired transferring ability', 'XPO:0141743', 'abnormal chemical homeostasis within a tissue', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(729195, 'HP:0031062', 'Impaired transferring ability', 'XPO:0101110', 'abnormal cell-free extract', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(729196, 'HP:0031062', 'Impaired transferring ability', 'XPO:0100377', 'abnormal connective tissue', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(729197, 'HP:0031062', 'Impaired transferring ability', 'XPO:0100724', 'abnormal kinetochore', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(729198, 'HP:0031062', 'Impaired transferring ability', 'XPO:0100802', 'abnormal exocrine cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(729199, 'HP:0031062', 'Impaired transferring ability', 'XPO:0131685', 'abnormal cortical actin cytoskeleton', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(729200, 'HP:0031062', 'Impaired transferring ability', 'XPO:0131469', 'abnormal heart process', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(729201, 'HP:0031062', 'Impaired transferring ability', 'XPO:0115509', 'abnormally semi-viable whole organism', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(729202, 'HP:0031062', 'Impaired transferring ability', 'XPO:0141975', 'abnormal cilium motility', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(729203, 'HP:0031062', 'Impaired transferring ability', 'XPO:0141962', 'absent cilium motility in pronephric kidney', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(729204, 'HP:0031062', 'Impaired transferring ability', 'XPO:0100907', 'abnormal cytoplasm', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(729205, 'HP:0031062', 'Impaired transferring ability', 'XPO:0100546', 'abnormal whole organism', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(729206, 'HP:0031062', 'Impaired transferring ability', 'XPO:0100862', 'abnormal blastomere V1', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(729207, 'HP:0031062', 'Impaired transferring ability', 'XPO:0100642', 'abnormal gustatory system', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(729208, 'HP:0031062', 'Impaired transferring ability', 'XPO:0107339', 'abnormal yolk platelet', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(729209, 'HP:0031062', 'Impaired transferring ability', 'XPO:0133403', 'abnormal developmental process', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(729210, 'HP:0031062', 'Impaired transferring ability', 'XPO:0131691', 'abnormal molecular function', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(729211, 'HP:0031062', 'Impaired transferring ability', 'XPO:0100006', 'abnormal anatomical structure', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(729212, 'HP:0031062', 'Impaired transferring ability', 'XPO:0141904', 'abnormal glucosamine metabolic process', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(729213, 'HP:0031062', 'Impaired transferring ability', 'XPO:0100784', 'abnormal left blastomere', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(729214, 'HP:0031062', 'Impaired transferring ability', 'XPO:0100721', 'abnormal centromere', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(729215, 'HP:0031062', 'Impaired transferring ability', 'XPO:0141777', 'abnormal catabolic process', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(729216, 'HP:0031062', 'Impaired transferring ability', 'XPO:0131740', 'abnormal detection of nodal flow', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(729217, 'HP:0031062', 'Impaired transferring ability', 'XPO:0101467', 'abnormal alkali secreting cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(729218, 'HP:0031062', 'Impaired transferring ability', 'XPO:0100762', 'abnormal intersomitic region', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(729219, 'HP:0031062', 'Impaired transferring ability', 'XPO:0100070', 'abnormal anatomical system', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(729220, 'HP:0031062', 'Impaired transferring ability', 'XPO:0131719', 'abnormal activation of meiosis', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(729221, 'HP:0031062', 'Impaired transferring ability', 'XPO:0131723', 'abnormal pathway-restricted SMAD protein phosphorylation', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(729222, 'HP:0031062', 'Impaired transferring ability', 'XPO:0101132', 'abnormal apoptotic cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(729223, 'HP:0031062', 'Impaired transferring ability', 'XPO:0100894', 'abnormal nucleus', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(729224, 'HP:0031062', 'Impaired transferring ability', 'XPO:0100307', 'abnormal blastomere', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(729225, 'HP:0031062', 'Impaired transferring ability', 'XPO:0100899', 'abnormal secondary spermatogonium', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(729226, 'HP:0031062', 'Impaired transferring ability', 'XPO:0131666', 'abnormal adherens junction', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(729227, 'HP:0031062', 'Impaired transferring ability', 'XPO:0100715', 'abnormal ciliated cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(729228, 'HP:0031062', 'Impaired transferring ability', 'XPO:0101347', 'abnormal hindlimb region', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(729229, 'HP:0031062', 'Impaired transferring ability', 'XPO:0107262', 'abnormal left-right axis', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(729230, 'HP:0031062', 'Impaired transferring ability', 'XPO:0100515', 'abnormal somatic stem cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(729231, 'HP:0031062', 'Impaired transferring ability', 'XPO:0101141', 'abnormal Keller explant', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(729232, 'HP:0031062', 'Impaired transferring ability', 'XPO:0100581', 'abnormal immune system', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(729233, 'HP:0031062', 'Impaired transferring ability', 'XPO:0141266', 'abnormal surface breathing', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(729234, 'HP:0031062', 'Impaired transferring ability', 'XPO:0141770', 'abnormal urate homeostasis', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(729235, 'HP:0031062', 'Impaired transferring ability', 'XPO:0100545', 'abnormal male organism', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(729236, 'HP:0031062', 'Impaired transferring ability', 'XPO:0107259', 'abnormal animal-vegetal axis', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(729237, 'HP:0031062', 'Impaired transferring ability', 'XPO:0101004', 'abnormal acid secreting cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(729238, 'HP:0031062', 'Impaired transferring ability', 'XPO:0141781', 'abnormal secondary metabolic process', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(729239, 'HP:0031062', 'Impaired transferring ability', 'XPO:0100547', 'abnormal blastomere V2', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(729240, 'HP:0031062', 'Impaired transferring ability', 'XPO:0141860', 'abnormal malate-aspartate shuttle', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(729241, 'HP:0031062', 'Impaired transferring ability', 'XPO:0141315', 'abnormal anatomical region', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(729242, 'HP:0031062', 'Impaired transferring ability', 'XPO:0100176', 'abnormal stage VI oocyte', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(729243, 'HP:0031062', 'Impaired transferring ability', 'XPO:0100551', 'abnormal oocyte cortex', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(729244, 'HP:0031062', 'Impaired transferring ability', 'XPO:0141600', 'absent metamorphosis', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(729245, 'HP:0031062', 'Impaired transferring ability', 'XPO:0101569', 'abnormal activin-induced ectoderm', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(729246, 'HP:0031062', 'Impaired transferring ability', 'XPO:0100205', 'abnormal limb segment', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(729247, 'HP:0031062', 'Impaired transferring ability', 'XPO:0107258', 'abnormal anatomical axis', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(729248, 'HP:0031062', 'Impaired transferring ability', 'XPO:00000000', 'Xenopus phenotype', 0.5714285714285714, 1.4755025719078136, 0.918228907628411, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(729249, 'HP:0031062', 'Impaired transferring ability', 'XPO:0141263', 'abnormal visually guided collision avoidance behavior', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(729250, 'HP:0031062', 'Impaired transferring ability', 'XPO:0141911', 'abnormal ribose phosphate metabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(729251, 'HP:0031062', 'Impaired transferring ability', 'XPO:0141771', 'abnormal urea homeostasis', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(729252, 'HP:0031062', 'Impaired transferring ability', 'XPO:0101448', 'abnormal myelin accumulating cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(729253, 'HP:0031062', 'Impaired transferring ability', 'XPO:0141791', 'abnormal primary metabolic process', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(729254, 'HP:0031062', 'Impaired transferring ability', 'XPO:0131730', 'abnormal regulation of protein folding', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(729255, 'HP:0031062', 'Impaired transferring ability', 'XPO:0131677', 'abnormal actin filament', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(729256, 'HP:0031062', 'Impaired transferring ability', 'XPO:0141795', 'abnormal glycosylation', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(729257, 'HP:0031062', 'Impaired transferring ability', 'XPO:0101072', 'abnormal mitochondrial cloud', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(729258, 'HP:0031062', 'Impaired transferring ability', 'XPO:0107272', 'abnormal axial region', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(729259, 'HP:0031062', 'Impaired transferring ability', 'XPO:0141877', 'abnormal 2-deoxyribose 1-phosphate metabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(729260, 'HP:0031062', 'Impaired transferring ability', 'XPO:0101411', 'abnormal marginal zone (sensu neural)', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(729261, 'HP:0031062', 'Impaired transferring ability', 'XPO:0141964', 'absent cilium motility in olfactory pit', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(729262, 'HP:0031062', 'Impaired transferring ability', 'XPO:0101297', 'abnormal barrier cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(729263, 'HP:0031062', 'Impaired transferring ability', 'XPO:0107270', 'abnormal proximal-distal axis', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(729264, 'HP:0031062', 'Impaired transferring ability', 'XPO:0100888', 'abnormal microtubule', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(729265, 'HP:0031062', 'Impaired transferring ability', 'XPO:0100308', 'abnormal early embryonic cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(729266, 'HP:0031062', 'Impaired transferring ability', 'XPO:0101513', 'abnormal basal body', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(729267, 'HP:0031062', 'Impaired transferring ability', 'XPO:0141264', 'abnormal schooling behavior', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(729268, 'HP:0031062', 'Impaired transferring ability', 'XPO:0141267', 'abnormal resting posture', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(729269, 'HP:0031062', 'Impaired transferring ability', 'XPO:0101373', 'abnormal oxygen accumulating cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(729270, 'HP:0031062', 'Impaired transferring ability', 'XPO:0107276', 'abnormal dorsal region', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(729271, 'HP:0031062', 'Impaired transferring ability', 'XPO:0141271', 'increased surface breathing', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(729272, 'HP:0031062', 'Impaired transferring ability', 'XPO:0100902', 'abnormal spermatocyte', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(729273, 'HP:0031062', 'Impaired transferring ability', 'XPO:0100289', 'abnormal chondroblast', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(729274, 'HP:0031062', 'Impaired transferring ability', 'XPO:0141776', 'abnormal metabolic process', 0.5263157894736842, 1.8210412618256888, 0.9790009036675816, 'HP:0000118', 'Phenotypic abnormality'),
(729275, 'HP:0031062', 'Impaired transferring ability', 'XPO:0141782', 'abnormal methylation', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(729276, 'HP:0031062', 'Impaired transferring ability', 'XPO:0131725', 'abnormal phosphorylation of RNA polymerase II C-terminal domain', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(729277, 'HP:0031062', 'Impaired transferring ability', 'XPO:0100317', 'abnormal respiratory system', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(729278, 'HP:0031062', 'Impaired transferring ability', 'XPO:0100465', 'abnormal skeletal system', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(729279, 'HP:0031062', 'Impaired transferring ability', 'XPO:0101302', 'abnormal subcortical cytoplasm', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(729280, 'HP:0031062', 'Impaired transferring ability', 'XPO:0131669', 'abnormal Roux spot', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(729281, 'HP:0031062', 'Impaired transferring ability', 'XPO:0100704', 'abnormal Merkel cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(729282, 'HP:0031062', 'Impaired transferring ability', 'XPO:0141276', 'decreased surface breathing', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(729283, 'HP:0031062', 'Impaired transferring ability', 'XPO:0133340', 'abnormal cell adhesion', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(729284, 'HP:0031062', 'Impaired transferring ability', 'XPO:0100239', 'abnormal acellular anatomical structure', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(729285, 'HP:0031062', 'Impaired transferring ability', 'XPO:0100427', 'abnormal olfactory system', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(729286, 'HP:0031062', 'Impaired transferring ability', 'XPO:0100218', 'abnormal epithelial cell', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(729287, 'HP:0031062', 'Impaired transferring ability', 'XPO:0141265', 'abnormal escape behavior', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(729288, 'HP:0031062', 'Impaired transferring ability', 'XPO:0100573', 'abnormal extraembryonic structure', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(729289, 'HP:0031062', 'Impaired transferring ability', 'XPO:0100423', 'abnormal process', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(729290, 'HP:0031062', 'Impaired transferring ability', 'XPO:0100202', 'abnormal embryo', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(729291, 'HP:0031062', 'Impaired transferring ability', 'XPO:0100081', 'abnormal anatomical entity in vitro', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(729292, 'HP:0031062', 'Impaired transferring ability', 'XPO:0101071', 'abnormal endoplasmic reticulum', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(729293, 'HP:0031062', 'Impaired transferring ability', 'XPO:0100587', 'abnormal vestibuloauditory system', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(729294, 'HP:0031062', 'Impaired transferring ability', 'XPO:0141775', 'abnormal nitrogen compound metabolic process', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(729295, 'HP:0031062', 'Impaired transferring ability', 'XPO:0101157', 'abnormal female organism', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(729296, 'HP:0031062', 'Impaired transferring ability', 'XPO:0141499', 'abnormal tadpole', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(729297, 'HP:0031062', 'Impaired transferring ability', 'XPO:0100104', 'abnormal embryonic structure', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(729298, 'HP:0031062', 'Impaired transferring ability', 'XPO:0100503', 'abnormal blastomere D2', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(729299, 'HP:0031062', 'Impaired transferring ability', 'XPO:0100477', 'abnormal pericyte', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(729300, 'HP:0031062', 'Impaired transferring ability', 'XPO:0101113', 'abnormal stage IV oocyte', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(729301, 'HP:0031062', 'Impaired transferring ability', 'XPO:0100823', 'abnormal blood', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(729302, 'HP:0031062', 'Impaired transferring ability', 'XPO:0100791', 'abnormal multiciliated cell precursor', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(729303, 'HP:0031062', 'Impaired transferring ability', 'XPO:0101366', 'abnormal morula cell', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(729304, 'HP:0031062', 'Impaired transferring ability', 'XPO:0107312', 'abnormal filopodium', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(729305, 'HP:0031062', 'Impaired transferring ability', 'XPO:0100501', 'abnormal urogenital system', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(729306, 'HP:0031062', 'Impaired transferring ability', 'XPO:0101240', 'abnormal ciliated non-epidermal cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(729307, 'HP:0031062', 'Impaired transferring ability', 'XPO:0116494', 'absent biological process', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(729308, 'HP:0031062', 'Impaired transferring ability', 'XPO:0100887', 'abnormal right-dorsal blastomere', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(729309, 'HP:0031062', 'Impaired transferring ability', 'XPO:0100691', 'abnormal keratin accumulating cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(729310, 'HP:0031062', 'Impaired transferring ability', 'XPO:0100585', 'abnormal elastica externa', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(729311, 'HP:0031062', 'Impaired transferring ability', 'XPO:0141738', 'abnormal carbon dioxide homeostasis', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(729312, 'HP:0031062', 'Impaired transferring ability', 'XPO:0100344', 'abnormal portion of organism substance', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(729313, 'HP:0031062', 'Impaired transferring ability', 'XPO:0100232', 'abnormal lymphatic system', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(729314, 'HP:0031062', 'Impaired transferring ability', 'XPO:0100392', 'abnormal cilium', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(729315, 'HP:0031062', 'Impaired transferring ability', 'XPO:0142057', 'abnormal desmosome', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(729316, 'HP:0031062', 'Impaired transferring ability', 'XPO:0141272', 'absent surface breathing', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(729317, 'HP:0031062', 'Impaired transferring ability', 'XPO:0101472', 'abnormal zygote cortex', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(729318, 'HP:0031062', 'Impaired transferring ability', 'XPO:0101480', 'abnormal stage V oocyte', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(729319, 'HP:0031062', 'Impaired transferring ability', 'XPO:0101283', 'abnormal left-ventral blastomere', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(729320, 'HP:0031062', 'Impaired transferring ability', 'XPO:0100674', 'abnormal secondary oogonium', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(729321, 'HP:0031062', 'Impaired transferring ability', 'XPO:0141892', 'abnormal inositol metabolic process', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(729322, 'HP:0031062', 'Impaired transferring ability', 'XPO:0141790', 'abnormal cellular metabolic process', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(729323, 'HP:0031062', 'Impaired transferring ability', 'XPO:0141745', 'abnormal creatinine homeostasis', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(729324, 'HP:0031062', 'Impaired transferring ability', 'XPO:0141907', 'abnormal putrescine metabolic process', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(729325, 'HP:0031062', 'Impaired transferring ability', 'XPO:0101264', 'abnormal mitotic spindle', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(729326, 'HP:0031062', 'Impaired transferring ability', 'XPO:0101435', 'abnormal paracrine cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(729327, 'HP:0031062', 'Impaired transferring ability', 'XPO:0100599', 'abnormal adult immune system', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(729328, 'HP:0031062', 'Impaired transferring ability', 'XPO:0101535', 'abnormal absorptive cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(729329, 'HP:0031062', 'Impaired transferring ability', 'XPO:0100969', 'abnormal disaggregated/reaggregated ectoderm treated with activin', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(729330, 'HP:0031062', 'Impaired transferring ability', 'XPO:0133388', 'absent insulin receptor signaling pathway', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(729331, 'HP:0031062', 'Impaired transferring ability', 'XPO:0101221', 'abnormal larval immune system', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(729332, 'HP:0031062', 'Impaired transferring ability', 'XPO:0100626', 'abnormal primordial germ cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(729333, 'HP:0031062', 'Impaired transferring ability', 'XPO:0131675', 'abnormal spindle microtubule', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(729334, 'HP:0031062', 'Impaired transferring ability', 'XPO:0141809', 'abnormal catalytic activity', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(729335, 'HP:0031062', 'Impaired transferring ability', 'XPO:0101451', 'abnormal dorsal lymph space', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(729336, 'HP:0031062', 'Impaired transferring ability', 'XPO:0100277', 'abnormal blastocoel', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(729337, 'HP:0031062', 'Impaired transferring ability', 'XPO:0101311', 'abnormal bottle cell', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(729338, 'HP:0031062', 'Impaired transferring ability', 'XPO:0141959', 'absent cilium motility in floor plate', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(729339, 'HP:0031062', 'Impaired transferring ability', 'XPO:0100481', 'abnormal anatomical line', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(729340, 'HP:0031062', 'Impaired transferring ability', 'XPO:0116434', 'abnormal biological process', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(729341, 'HP:0031062', 'Impaired transferring ability', 'XPO:0101136', 'abnormal ooplasm', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(729342, 'HP:0031062', 'Impaired transferring ability', 'XPO:0101570', 'abnormal forelimb region', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(729343, 'HP:0031062', 'Impaired transferring ability', 'XPO:0133401', 'absent determination of left/right symmetry in lateral plate mesoderm', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(729344, 'HP:0031062', 'Impaired transferring ability', 'XPO:0115505', 'dead whole organism', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(729345, 'HP:0031062', 'Impaired transferring ability', 'XPO:0141772', 'abnormal water homeostasis', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(729346, 'HP:0031062', 'Impaired transferring ability', 'XPO:0115512', 'abnormally semi-erect whole organism', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(729347, 'HP:0031062', 'Impaired transferring ability', 'XPO:0107260', 'abnormal anterior-posterior axis', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(729348, 'HP:0031062', 'Impaired transferring ability', 'XPO:0100084', 'abnormal anatomical group', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(729349, 'HP:0031062', 'Impaired transferring ability', 'XPO:0100688', 'abnormal adipose tissue', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(729350, 'HP:0031062', 'Impaired transferring ability', 'XPO:0141783', 'abnormal collagen metabolic process', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(729351, 'HP:0031062', 'Impaired transferring ability', 'XPO:0101468', 'abnormal stage I oocyte', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(729352, 'HP:0031062', 'Impaired transferring ability', 'XPO:0101228', 'abnormal mesenchymal stem cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(729353, 'HP:0031062', 'Impaired transferring ability', 'XPO:0100638', 'abnormal polar body', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(729354, 'HP:0031062', 'Impaired transferring ability', 'XPO:0116433', 'abnormal axis specification', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(729355, 'HP:0031062', 'Impaired transferring ability', 'XPO:0107253', 'abnormal enteric nervous system', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(729356, 'HP:0031062', 'Impaired transferring ability', 'XPO:0100274', 'abnormal sensory system', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(729357, 'HP:0031062', 'Impaired transferring ability', 'XPO:0100417', 'abnormal dense regular connective tissue', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(729358, 'HP:0031062', 'Impaired transferring ability', 'XPO:0100422', 'abnormal notochord', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(729359, 'HP:0031062', 'Impaired transferring ability', 'XPO:0100003', 'abnormal organism subdivision', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(729360, 'HP:0031062', 'Impaired transferring ability', 'XPO:0101109', 'abnormal egg cell-free extract', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(729361, 'HP:0031062', 'Impaired transferring ability', 'XPO:0141778', 'abnormal biosynthetic process', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(729362, 'HP:0031062', 'Impaired transferring ability', 'XPO:0107273', 'abnormal basal region', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(729363, 'HP:0031062', 'Impaired transferring ability', 'XPO:0131745', 'abnormal axis elongation', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(729364, 'HP:0031062', 'Impaired transferring ability', 'XPO:0100028', 'abnormal anatomical cluster', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(729365, 'HP:0031062', 'Impaired transferring ability', 'XPO:0116429', 'abnormal behavior', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(729366, 'HP:0031062', 'Impaired transferring ability', 'XPO:0101333', 'abnormal barrier epithelial cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(729367, 'HP:0031062', 'Impaired transferring ability', 'XPO:0101389', 'abnormal wedge region', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(729368, 'HP:0031062', 'Impaired transferring ability', 'XPO:0141794', 'abnormal prosthetic group metabolic process', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(729369, 'HP:0031062', 'Impaired transferring ability', 'XPO:0100031', 'abnormal central nervous system', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(729370, 'HP:0031062', 'Impaired transferring ability', 'XPO:0101237', 'abnormal mucus secreting cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(729371, 'HP:0031062', 'Impaired transferring ability', 'XPO:0101220', 'abnormal centriole', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(729372, 'HP:0031062', 'Impaired transferring ability', 'XPO:0101575', 'abnormal vitelline membrane', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(729373, 'HP:0031062', 'Impaired transferring ability', 'XPO:0101326', 'abnormal cementoblast', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(729374, 'HP:0031062', 'Impaired transferring ability', 'XPO:0100549', 'abnormal mitotic cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(729375, 'HP:0031062', 'Impaired transferring ability', 'XPO:0100152', 'abnormal alimentary system', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(729376, 'HP:0031062', 'Impaired transferring ability', 'XPO:0100372', 'abnormal hematological system', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(729377, 'HP:0031062', 'Impaired transferring ability', 'XPO:0141798', 'abnormal lipid metabolic process', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(729378, 'HP:0031062', 'Impaired transferring ability', 'XPO:0141724', 'abnormal prevention of polyspermy', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(729379, 'HP:0031062', 'Impaired transferring ability', 'XPO:0100533', 'abnormal melanoblast', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(729380, 'HP:0031062', 'Impaired transferring ability', 'XPO:0100285', 'abnormal progenitor cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(729381, 'HP:0031062', 'Impaired transferring ability', 'XPO:0141898', 'abnormal maltose metabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(729382, 'HP:0031062', 'Impaired transferring ability', 'XPO:0141960', 'absent cilium motility in brain', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(729383, 'HP:0031062', 'Impaired transferring ability', 'XPO:0100225', 'abnormal endocrine system', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(729384, 'HP:0031062', 'Impaired transferring ability', 'XPO:0101200', 'abnormal joint region', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(729385, 'HP:0031062', 'Impaired transferring ability', 'XPO:0100273', 'abnormal visual system', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(729386, 'HP:0031062', 'Impaired transferring ability', 'XPO:0100010', 'abnormal multicellular anatomical structure', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(729387, 'HP:0031062', 'Impaired transferring ability', 'XPO:0100665', 'abnormal egg jelly', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(729388, 'HP:0031062', 'Impaired transferring ability', 'XPO:0107261', 'abnormal dorsal-ventral axis', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(729389, 'HP:0031062', 'Impaired transferring ability', 'XPO:0100032', 'abnormal nervous system', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(729390, 'HP:0031062', 'Impaired transferring ability', 'XPO:0107271', 'abnormal apical region', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(729391, 'HP:0031062', 'Impaired transferring ability', 'XPO:0101241', 'abnormal nucleate erythrocyte', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(729392, 'HP:0031062', 'Impaired transferring ability', 'XPO:0107278', 'abnormal medial region', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(729393, 'HP:0031062', 'Impaired transferring ability', 'XPO:0100989', 'abnormal right blastomere', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(729394, 'HP:0031062', 'Impaired transferring ability', 'XPO:0107284', 'abnormal migrating myoblast', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(729395, 'HP:0031062', 'Impaired transferring ability', 'XPO:0100917', 'abnormal stage III oocyte', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(729396, 'HP:0031062', 'Impaired transferring ability', 'XPO:0100643', 'abnormal thoracic region', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(729397, 'HP:0031062', 'Impaired transferring ability', 'XPO:0100842', 'abnormal left-dorsal blastomere', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(729398, 'HP:0031062', 'Impaired transferring ability', 'XPO:0100754', 'abnormal electrically active cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(729399, 'HP:0031062', 'Impaired transferring ability', 'XPO:0100295', 'abnormal extracellular matrix', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(729400, 'HP:0031062', 'Impaired transferring ability', 'XPO:0100653', 'abnormal myoblast', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(729401, 'HP:0031062', 'Impaired transferring ability', 'XPO:0131687', 'abnormal astral microtubule', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(729402, 'HP:0031062', 'Impaired transferring ability', 'XPO:0100956', 'abnormal centrosome', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(729403, 'HP:0031062', 'Impaired transferring ability', 'XPO:0101061', 'abnormal plasma membrane', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(729404, 'HP:0031062', 'Impaired transferring ability', 'XPO:0101409', 'abnormal perivitelline space', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(729405, 'HP:0031062', 'Impaired transferring ability', 'XPO:0100976', 'abnormal multiciliated cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(729406, 'HP:0031062', 'Impaired transferring ability', 'XPO:0131744', 'abnormal apical constriction', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(729407, 'HP:0031062', 'Impaired transferring ability', 'XPO:0141796', 'abnormal demethylation', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(729408, 'HP:0031062', 'Impaired transferring ability', 'XPO:0100574', 'abnormal gastrula cell', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(729409, 'HP:0031062', 'Impaired transferring ability', 'XPO:0101463', 'abnormal right-ventral blastomere', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(729410, 'HP:0031062', 'Impaired transferring ability', 'XPO:0101547', 'abnormal lampbrush chromosome', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(729411, 'HP:0031062', 'Impaired transferring ability', 'XPO:0101461', 'abnormal sperm entry point', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(729412, 'HP:0031062', 'Impaired transferring ability', 'XPO:0100258', 'abnormal organ part', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(729413, 'HP:0031062', 'Impaired transferring ability', 'XPO:0107263', 'abnormal anatomical side', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(729414, 'HP:0031062', 'Impaired transferring ability', 'XPO:0100429', 'abnormal spermatid', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(729415, 'HP:0031062', 'Impaired transferring ability', 'XPO:0141784', 'abnormal cellular hormone metabolic process', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(729416, 'HP:0031062', 'Impaired transferring ability', 'XPO:0141797', 'abnormal hydrogen metabolic process', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(729417, 'HP:0031062', 'Impaired transferring ability', 'XPO:0141748', 'abnormal gas homeostasis', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(729418, 'HP:0031062', 'Impaired transferring ability', 'XPO:0141786', 'abnormal pigment metabolic process', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(729419, 'HP:0031062', 'Impaired transferring ability', 'XPO:0100025', 'abnormal oocyte', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(729420, 'HP:0031062', 'Impaired transferring ability', 'XPO:0100337', 'abnormal zygote', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(729421, 'HP:0031062', 'Impaired transferring ability', 'XPO:0100437', 'abnormal proepicardium', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(729422, 'HP:0031062', 'Impaired transferring ability', 'XPO:0100108', 'abnormal cell part', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(729423, 'HP:0031062', 'Impaired transferring ability', 'XPO:0100852', 'abnormal interdigital region', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(729424, 'HP:0031062', 'Impaired transferring ability', 'XPO:0131722', 'abnormal determination of left/right symmetry', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(729425, 'HP:0031062', 'Impaired transferring ability', 'XPO:0100172', 'abnormal stem cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(729426, 'HP:0031062', 'Impaired transferring ability', 'XPO:0101378', 'abnormal blastomere D1', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(729427, 'HP:0031062', 'Impaired transferring ability', 'XPO:0128000', 'absent behavior', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(729428, 'HP:0031062', 'Impaired transferring ability', 'XPO:0141958', 'absent cilium motility in left-right organizer', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(729429, 'HP:0031062', 'Impaired transferring ability', 'XPO:0141792', 'abnormal small molecule metabolic process', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(729430, 'HP:0031062', 'Impaired transferring ability', 'XPO:0101405', 'abnormal ring structure', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(729431, 'HP:0031062', 'Impaired transferring ability', 'XPO:0101497', 'abnormal ciliary axoneme', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(729432, 'HP:0031062', 'Impaired transferring ability', 'XPO:0141754', 'abnormal homeostatic process', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(729433, 'HP:0031062', 'Impaired transferring ability', 'XPO:0100026', 'abnormal germ cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(729434, 'HP:0031062', 'Impaired transferring ability', 'XPO:0101498', 'abnormal stage II oocyte', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(729435, 'HP:0031062', 'Impaired transferring ability', 'XPO:0100009', 'abnormal multi-tissue structure', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(729436, 'HP:0031062', 'Impaired transferring ability', 'XPO:0115508', 'abnormally peramorphic growth of whole organism', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(729437, 'HP:0031062', 'Impaired transferring ability', 'XPO:0100062', 'abnormal anatomical space', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(729438, 'HP:0031062', 'Impaired transferring ability', 'XPO:0131667', 'abnormal actin cytoskeleton', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(729439, 'HP:0031401', 'Reduced proportion of CD4-negative, CD8-negative, alpha-beta regulatory T cells', 'XPO:0131005', 'abnormally increased number of thymocyte', 0.5348837209302325, 9.586341000560333, 2.264415541477703, 'HP:0011839', 'Abnormal T cell count'),
(729440, 'HP:0031401', 'Reduced proportion of CD4-negative, CD8-negative, alpha-beta regulatory T cells', 'XPO:0140117', 'abnormally necrotic thymocyte', 0.4090909090909091, 9.260765128657825, 1.9464056168640749, 'HP:0002843', 'Abnormal T cell morphology'),
(729441, 'HP:0031401', 'Reduced proportion of CD4-negative, CD8-negative, alpha-beta regulatory T cells', 'XPO:0125284', 'absent thymocyte', 0.5974025974025974, 9.586341000560333, 2.39309527878055, 'HP:0011839', 'Abnormal T cell count'),
(729442, 'HP:0031401', 'Reduced proportion of CD4-negative, CD8-negative, alpha-beta regulatory T cells', 'XPO:0131221', 'abnormally decreased number of thymocyte', 0.5287356321839081, 9.586341000560333, 2.2513640463642894, 'HP:0011839', 'Abnormal T cell count'),
(729443, 'HP:0031401', 'Reduced proportion of CD4-negative, CD8-negative, alpha-beta regulatory T cells', 'XPO:0102080', 'abnormal thymocyte morphology', 0.43373493975903615, 9.260765128657825, 2.004174993657237, 'HP:0002843', 'Abnormal T cell morphology'),
(729444, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0102207', 'abnormal diencephalon morphology', 0.4090909090909091, 6.667568321314008, 1.6515573214369805, 'HP:0100547', 'Abnormal forebrain morphology'),
(729445, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0128708', 'decreased size of the basal forebrain', 0.4084507042253521, 8.02346099791745, 1.810300608993995, 'HP:0002060', 'Abnormal cerebral morphology'),
(729446, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0100194', 'abnormal preoptic area', 0.43548387096774194, 6.667568321314008, 1.704000722566664, 'HP:0100547', 'Abnormal forebrain morphology'),
(729447, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0100473', 'abnormal ventral habenular nucleus', 0.4153846153846154, 6.667568321314008, 1.6642131181731699, 'HP:0100547', 'Abnormal forebrain morphology'),
(729448, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0102191', 'abnormal telencephalon morphology', 0.4603174603174603, 8.02346099791745, 1.9218062310018553, 'HP:0002060', 'Abnormal cerebral morphology'),
(729449, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0100491', 'abnormal pars distalis', 0.421875, 6.667568321314008, 1.677164388351466, 'HP:0100547', 'Abnormal forebrain morphology'),
(729450, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0128739', 'decreased size of the dorsal telencephalon', 0.4084507042253521, 8.02346099791745, 1.810300608993995, 'HP:0002060', 'Abnormal cerebral morphology'),
(729451, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0102247', 'abnormal mitral cell layer of the olfactory bulb morphology', 0.4027777777777778, 8.02346099791745, 1.7976851200440698, 'HP:0002060', 'Abnormal cerebral morphology'),
(729452, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0141224', 'abnormally necrotic dorsal telencephalon', 0.42028985507246375, 8.02346099791745, 1.8363494384224073, 'HP:0002060', 'Abnormal cerebral morphology'),
(729453, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0141149', 'abnormally necrotic dorsal pallium', 0.4142857142857143, 8.02346099791745, 1.8231854734408677, 'HP:0002060', 'Abnormal cerebral morphology'),
(729454, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0140574', 'abnormally necrotic medial ganglionic eminence', 0.4084507042253521, 8.02346099791745, 1.810300608993995, 'HP:0002060', 'Abnormal cerebral morphology'),
(729455, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0102854', 'abnormal medial septum morphology', 0.42028985507246375, 8.02346099791745, 1.8363494384224073, 'HP:0002060', 'Abnormal cerebral morphology'),
(729456, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0130082', 'increased size of the subpallium', 0.4084507042253521, 8.02346099791745, 1.810300608993995, 'HP:0002060', 'Abnormal cerebral morphology'),
(729457, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0102826', 'abnormal anterior commissure morphology', 0.4461538461538462, 8.02346099791745, 1.8920089808682852, 'HP:0002060', 'Abnormal cerebral morphology'),
(729458, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0102986', 'abnormal eminentia thalami morphology', 0.40298507462686567, 6.667568321314008, 1.639185931352649, 'HP:0100547', 'Abnormal forebrain morphology'),
(729459, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0139879', 'abnormally necrotic telencephalon', 0.4264705882352941, 8.02346099791745, 1.8498027277157947, 'HP:0002060', 'Abnormal cerebral morphology'),
(729460, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0101652', 'abnormal external plexiform layer of the olfactory bulb morphology', 0.4027777777777778, 8.02346099791745, 1.7976851200440698, 'HP:0002060', 'Abnormal cerebral morphology'),
(729461, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0100611', 'abnormal hypophysis', 0.43548387096774194, 6.667568321314008, 1.704000722566664, 'HP:0100547', 'Abnormal forebrain morphology'),
(729462, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0102357', 'abnormal subpallium morphology', 0.453125, 8.02346099791745, 1.9067330082319718, 'HP:0002060', 'Abnormal cerebral morphology'),
(729463, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0100695', 'abnormal zona limitans intrathalamica', 0.4426229508196721, 6.667568321314008, 1.7179111633526845, 'HP:0100547', 'Abnormal forebrain morphology'),
(729464, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0100698', 'abnormal optic stalk', 0.43548387096774194, 6.667568321314008, 1.704000722566664, 'HP:0100547', 'Abnormal forebrain morphology'),
(729465, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0101293', 'abnormal posterior hypothalamus', 0.4426229508196721, 6.667568321314008, 1.7179111633526845, 'HP:0100547', 'Abnormal forebrain morphology'),
(729466, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0101664', 'abnormal nervous system morphology', 0.41304347826086957, 4.7814666189787065, 1.405330425021534, 'HP:0012639', 'Abnormal nervous system morphology'),
(729467, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0140544', 'abnormally necrotic forebrain', 0.40298507462686567, 6.667568321314008, 1.639185931352649, 'HP:0100547', 'Abnormal forebrain morphology'),
(729468, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0100914', 'abnormal pars intermedia', 0.421875, 6.667568321314008, 1.677164388351466, 'HP:0100547', 'Abnormal forebrain morphology'),
(729469, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0128444', 'decreased size of the telencephalon', 0.4142857142857143, 8.02346099791745, 1.8231854734408677, 'HP:0002060', 'Abnormal cerebral morphology'),
(729470, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0130903', 'increased size of the anterior commissure', 0.4027777777777778, 8.02346099791745, 1.7976851200440698, 'HP:0002060', 'Abnormal cerebral morphology'),
(729471, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0100971', 'abnormal prethalamus basal plate', 0.42857142857142855, 6.667568321314008, 1.6904228111816126, 'HP:0100547', 'Abnormal forebrain morphology'),
(729472, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0100263', 'abnormal prethalamus', 0.4426229508196721, 6.667568321314008, 1.7179111633526845, 'HP:0100547', 'Abnormal forebrain morphology'),
(729473, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0130873', 'increased size of the medial pallium', 0.4027777777777778, 8.02346099791745, 1.7976851200440698, 'HP:0002060', 'Abnormal cerebral morphology'),
(729474, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0128429', 'decreased size of the pallium', 0.4084507042253521, 8.02346099791745, 1.810300608993995, 'HP:0002060', 'Abnormal cerebral morphology'),
(729475, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0102442', 'abnormal medial pallium morphology', 0.4461538461538462, 8.02346099791745, 1.8920089808682852, 'HP:0002060', 'Abnormal cerebral morphology'),
(729476, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0102389', 'abnormal bed nucleus of the stria terminalis morphology', 0.4084507042253521, 8.02346099791745, 1.810300608993995, 'HP:0002060', 'Abnormal cerebral morphology'),
(729477, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0102200', 'abnormal telencephalon septum morphology', 0.4264705882352941, 8.02346099791745, 1.8498027277157947, 'HP:0002060', 'Abnormal cerebral morphology'),
(729478, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0100909', 'abnormal choroid fissure', 0.4090909090909091, 6.667568321314008, 1.6515573214369805, 'HP:0100547', 'Abnormal forebrain morphology'),
(729479, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0131746', 'abnormal neural tube closure', 0.4117647058823529, 5.483278994082134, 1.502604659339613, 'HP:0002011', 'Morphological central nervous system abnormality'),
(729480, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0102066', 'abnormal ventral pallium morphology', 0.4461538461538462, 8.02346099791745, 1.8920089808682852, 'HP:0002060', 'Abnormal cerebral morphology'),
(729481, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0101838', 'abnormal nucleus accumbens morphology', 0.4142857142857143, 8.02346099791745, 1.8231854734408677, 'HP:0002060', 'Abnormal cerebral morphology'),
(729482, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0139993', 'abnormally necrotic pallidum', 0.4027777777777778, 8.02346099791745, 1.7976851200440698, 'HP:0002060', 'Abnormal cerebral morphology'),
(729483, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0100998', 'abnormal rostral tuberal region', 0.42857142857142855, 6.667568321314008, 1.6904228111816126, 'HP:0100547', 'Abnormal forebrain morphology'),
(729484, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0100233', 'abnormal pars nervosa', 0.421875, 6.667568321314008, 1.677164388351466, 'HP:0100547', 'Abnormal forebrain morphology'),
(729485, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0128704', 'decreased size of the lateral pallium', 0.4027777777777778, 8.02346099791745, 1.7976851200440698, 'HP:0002060', 'Abnormal cerebral morphology'),
(729486, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0102509', 'abnormal lateral septum morphology', 0.42028985507246375, 8.02346099791745, 1.8363494384224073, 'HP:0002060', 'Abnormal cerebral morphology'),
(729487, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0102584', 'abnormal dorsal septum morphology', 0.42028985507246375, 8.02346099791745, 1.8363494384224073, 'HP:0002060', 'Abnormal cerebral morphology'),
(729488, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0101790', 'abnormal neuromere morphology', 0.42, 5.483278994082134, 1.5175563177406288, 'HP:0002011', 'Morphological central nervous system abnormality'),
(729489, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0130846', 'increased size of the anterior entopeduncular region', 0.43283582089552236, 8.02346099791745, 1.8635560972122107, 'HP:0002060', 'Abnormal cerebral morphology'),
(729490, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0130187', 'increased size of the basal forebrain', 0.4084507042253521, 8.02346099791745, 1.810300608993995, 'HP:0002060', 'Abnormal cerebral morphology'),
(729491, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0140029', 'abnormally necrotic basal forebrain', 0.42028985507246375, 8.02346099791745, 1.8363494384224073, 'HP:0002060', 'Abnormal cerebral morphology'),
(729492, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0102604', 'abnormal ventral pallidum morphology', 0.4264705882352941, 8.02346099791745, 1.8498027277157947, 'HP:0002060', 'Abnormal cerebral morphology'),
(729493, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0101663', 'abnormal central nervous system morphology', 0.4375, 5.483278994082134, 1.5488494310006167, 'HP:0002011', 'Morphological central nervous system abnormality'),
(729494, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0142037', 'decreased size of the cerebrospinal fluid', 0.40384615384615385, 5.483278994082134, 1.4880863994491305, 'HP:0002011', 'Morphological central nervous system abnormality'),
(729495, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0101496', 'abnormal subcommissural organ', 0.4426229508196721, 6.667568321314008, 1.7179111633526845, 'HP:0100547', 'Abnormal forebrain morphology'),
(729496, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0102951', 'abnormal lateral amygdala morphology', 0.42028985507246375, 8.02346099791745, 1.8363494384224073, 'HP:0002060', 'Abnormal cerebral morphology'),
(729497, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0101443', 'abnormal subthalamic nucleus', 0.40298507462686567, 6.667568321314008, 1.639185931352649, 'HP:0100547', 'Abnormal forebrain morphology'),
(729498, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0101354', 'abnormal eminentia thalami', 0.45, 6.667568321314008, 1.7321679319833003, 'HP:0100547', 'Abnormal forebrain morphology'),
(729499, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0100575', 'abnormal diencephalon', 0.4576271186440678, 6.667568321314008, 1.7467856420423753, 'HP:0100547', 'Abnormal forebrain morphology'),
(729500, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0101075', 'abnormal mammilary region', 0.43548387096774194, 6.667568321314008, 1.704000722566664, 'HP:0100547', 'Abnormal forebrain morphology'),
(729501, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0128602', 'decreased size of the subpallium', 0.4084507042253521, 8.02346099791745, 1.810300608993995, 'HP:0002060', 'Abnormal cerebral morphology'),
(729502, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0101068', 'abnormal pineal gland', 0.4090909090909091, 6.667568321314008, 1.6515573214369805, 'HP:0100547', 'Abnormal forebrain morphology'),
(729503, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0101797', 'abnormal lateral pallium morphology', 0.4461538461538462, 8.02346099791745, 1.8920089808682852, 'HP:0002060', 'Abnormal cerebral morphology'),
(729504, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0100946', 'abnormal melanotrope', 0.4090909090909091, 6.667568321314008, 1.6515573214369805, 'HP:0100547', 'Abnormal forebrain morphology'),
(729505, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0103107', 'abnormal ventral septum morphology', 0.42028985507246375, 8.02346099791745, 1.8363494384224073, 'HP:0002060', 'Abnormal cerebral morphology'),
(729506, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0129372', 'decreased size of the anterior entopeduncular region', 0.43283582089552236, 8.02346099791745, 1.8635560972122107, 'HP:0002060', 'Abnormal cerebral morphology'),
(729507, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0102249', 'abnormal forebrain morphology', 0.43548387096774194, 6.667568321314008, 1.704000722566664, 'HP:0100547', 'Abnormal forebrain morphology'),
(729508, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0129429', 'decreased size of the anterior commissure', 0.4027777777777778, 8.02346099791745, 1.7976851200440698, 'HP:0002060', 'Abnormal cerebral morphology'),
(729509, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0100656', 'abnormal ventral hypothalamic nucleus', 0.42857142857142855, 6.667568321314008, 1.6904228111816126, 'HP:0100547', 'Abnormal forebrain morphology'),
(729510, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0102238', 'abnormal basal forebrain morphology', 0.453125, 8.02346099791745, 1.9067330082319718, 'HP:0002060', 'Abnormal cerebral morphology'),
(729511, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0103133', 'abnormal parabrachial area morphology', 0.4117647058823529, 5.483278994082134, 1.502604659339613, 'HP:0002011', 'Morphological central nervous system abnormality'),
(729512, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0101671', 'abnormal olfactory bulb morphology', 0.4027777777777778, 8.02346099791745, 1.7976851200440698, 'HP:0002060', 'Abnormal cerebral morphology'),
(729513, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0101805', 'abnormal pallidum morphology', 0.43283582089552236, 8.02346099791745, 1.8635560972122107, 'HP:0002060', 'Abnormal cerebral morphology'),
(729514, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0101186', 'abnormal optic chiasm', 0.45, 6.667568321314008, 1.7321679319833003, 'HP:0100547', 'Abnormal forebrain morphology'),
(729515, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0129924', 'increased size of the telencephalon', 0.4142857142857143, 8.02346099791745, 1.8231854734408677, 'HP:0002060', 'Abnormal cerebral morphology'),
(729516, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0101588', 'abnormal central nucleus of the thalamus', 0.42857142857142855, 6.667568321314008, 1.6904228111816126, 'HP:0100547', 'Abnormal forebrain morphology'),
(729517, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0130217', 'increased size of the dorsal telencephalon', 0.4084507042253521, 8.02346099791745, 1.810300608993995, 'HP:0002060', 'Abnormal cerebral morphology'),
(729518, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0142031', 'abnormally necrotic cerebrospinal fluid', 0.42, 5.483278994082134, 1.5175563177406288, 'HP:0002011', 'Morphological central nervous system abnormality'),
(729519, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0100988', 'abnormal habenula', 0.43548387096774194, 6.667568321314008, 1.704000722566664, 'HP:0100547', 'Abnormal forebrain morphology'),
(729520, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0100157', 'abnormal optic tract', 0.45, 6.667568321314008, 1.7321679319833003, 'HP:0100547', 'Abnormal forebrain morphology'),
(729521, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0126877', 'abnormally localised diencephalon', 0.40298507462686567, 6.667568321314008, 1.639185931352649, 'HP:0100547', 'Abnormal forebrain morphology'),
(729522, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0101117', 'abnormal tuberal region', 0.43548387096774194, 6.667568321314008, 1.704000722566664, 'HP:0100547', 'Abnormal forebrain morphology'),
(729523, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0102760', 'abnormal dorsal pallidum morphology', 0.4264705882352941, 8.02346099791745, 1.8498027277157947, 'HP:0002060', 'Abnormal cerebral morphology'),
(729524, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0107380', 'abnormal dorsal telencephalon morphology', 0.453125, 8.02346099791745, 1.9067330082319718, 'HP:0002060', 'Abnormal cerebral morphology'),
(729525, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0129962', 'increased size of the ventral pallium', 0.4027777777777778, 8.02346099791745, 1.7976851200440698, 'HP:0002060', 'Abnormal cerebral morphology'),
(729526, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0101140', 'abnormal ventrolateral thalamic nucleus', 0.42857142857142855, 6.667568321314008, 1.6904228111816126, 'HP:0100547', 'Abnormal forebrain morphology'),
(729527, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0140021', 'abnormally necrotic striatum', 0.4027777777777778, 8.02346099791745, 1.7976851200440698, 'HP:0002060', 'Abnormal cerebral morphology'),
(729528, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0102131', 'abnormal glomerular layer of the olfactory bulb morphology', 0.4027777777777778, 8.02346099791745, 1.7976851200440698, 'HP:0002060', 'Abnormal cerebral morphology'),
(729529, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0101796', 'abnormal neural nucleus morphology', 0.42857142857142855, 5.483278994082134, 1.5329633758669794, 'HP:0002011', 'Morphological central nervous system abnormality'),
(729530, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0101526', 'abnormal infundibulum', 0.43548387096774194, 6.667568321314008, 1.704000722566664, 'HP:0100547', 'Abnormal forebrain morphology'),
(729531, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0101906', 'abnormal sensory system morphology', 0.40425531914893614, 4.7814666189787065, 1.3902997209433732, 'HP:0012639', 'Abnormal nervous system morphology'),
(729532, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0140854', 'abnormally necrotic ventral pallium', 0.4142857142857143, 8.02346099791745, 1.8231854734408677, 'HP:0002060', 'Abnormal cerebral morphology'),
(729533, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0139760', 'abnormally necrotic basal ganglion', 0.4084507042253521, 8.02346099791745, 1.810300608993995, 'HP:0002060', 'Abnormal cerebral morphology'),
(729534, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0101564', 'abnormal anterior thalamic nucleus', 0.42857142857142855, 6.667568321314008, 1.6904228111816126, 'HP:0100547', 'Abnormal forebrain morphology'),
(729535, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0140186', 'abnormally necrotic pallium', 0.42028985507246375, 8.02346099791745, 1.8363494384224073, 'HP:0002060', 'Abnormal cerebral morphology'),
(729536, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0102696', 'abnormal accessory olfactory bulb morphology', 0.4084507042253521, 8.02346099791745, 1.810300608993995, 'HP:0002060', 'Abnormal cerebral morphology'),
(729537, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0100729', 'abnormal thalamus', 0.45, 6.667568321314008, 1.7321679319833003, 'HP:0100547', 'Abnormal forebrain morphology'),
(729538, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0103040', 'abnormal nucleus of the diagonal band morphology', 0.4264705882352941, 8.02346099791745, 1.8498027277157947, 'HP:0002060', 'Abnormal cerebral morphology'),
(729539, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0101268', 'abnormal lateral hypothalamic nucleus', 0.42857142857142855, 6.667568321314008, 1.6904228111816126, 'HP:0100547', 'Abnormal forebrain morphology'),
(729540, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0100195', 'abnormal retromammillary area', 0.4426229508196721, 6.667568321314008, 1.7179111633526845, 'HP:0100547', 'Abnormal forebrain morphology'),
(729541, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0101284', 'abnormal ventromedial thalamic nucleus', 0.42857142857142855, 6.667568321314008, 1.6904228111816126, 'HP:0100547', 'Abnormal forebrain morphology'),
(729542, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0100315', 'abnormal neurohypophysis', 0.42857142857142855, 6.667568321314008, 1.6904228111816126, 'HP:0100547', 'Abnormal forebrain morphology'),
(729543, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0101987', 'abnormal striatum morphology', 0.43283582089552236, 8.02346099791745, 1.8635560972122107, 'HP:0002060', 'Abnormal cerebral morphology'),
(729544, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0129399', 'decreased size of the medial pallium', 0.4027777777777778, 8.02346099791745, 1.7976851200440698, 'HP:0002060', 'Abnormal cerebral morphology'),
(729545, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0140226', 'abnormally necrotic subpallium', 0.42028985507246375, 8.02346099791745, 1.8363494384224073, 'HP:0002060', 'Abnormal cerebral morphology'),
(729546, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0129909', 'increased size of the pallium', 0.4084507042253521, 8.02346099791745, 1.810300608993995, 'HP:0002060', 'Abnormal cerebral morphology'),
(729547, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0102968', 'abnormal medial ganglionic eminence morphology', 0.4393939393939394, 8.02346099791745, 1.8776208710622537, 'HP:0002060', 'Abnormal cerebral morphology'),
(729548, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0100783', 'abnormal supraoptoparaventricular region', 0.421875, 6.667568321314008, 1.677164388351466, 'HP:0100547', 'Abnormal forebrain morphology'),
(729549, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0140476', 'abnormally necrotic lateral ganglionic eminence', 0.4084507042253521, 8.02346099791745, 1.810300608993995, 'HP:0002060', 'Abnormal cerebral morphology'),
(729550, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0101420', 'abnormal magnocellular preoptic nucleus', 0.4153846153846154, 6.667568321314008, 1.6642131181731699, 'HP:0100547', 'Abnormal forebrain morphology'),
(729551, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0140045', 'abnormally necrotic lateral pallium', 0.4142857142857143, 8.02346099791745, 1.8231854734408677, 'HP:0002060', 'Abnormal cerebral morphology'),
(729552, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0102174', 'abnormal pallium morphology', 0.453125, 8.02346099791745, 1.9067330082319718, 'HP:0002060', 'Abnormal cerebral morphology'),
(729553, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0100951', 'abnormal adenohypophysis', 0.42857142857142855, 6.667568321314008, 1.6904228111816126, 'HP:0100547', 'Abnormal forebrain morphology'),
(729554, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0101351', 'abnormal dorsal habenular nucleus', 0.4153846153846154, 6.667568321314008, 1.6642131181731699, 'HP:0100547', 'Abnormal forebrain morphology'),
(729555, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0130183', 'increased size of the lateral pallium', 0.4027777777777778, 8.02346099791745, 1.7976851200440698, 'HP:0002060', 'Abnormal cerebral morphology'),
(729556, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0142058', 'abnormal cerebrospinal fluid morphology', 0.44680851063829785, 5.483278994082134, 1.5652398285119449, 'HP:0002011', 'Morphological central nervous system abnormality'),
(729557, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0142044', 'increased size of the cerebrospinal fluid', 0.40384615384615385, 5.483278994082134, 1.4880863994491305, 'HP:0002011', 'Morphological central nervous system abnormality'),
(729558, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0103057', 'abnormal medial amygdala morphology', 0.42028985507246375, 8.02346099791745, 1.8363494384224073, 'HP:0002060', 'Abnormal cerebral morphology'),
(729559, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0102007', 'abnormal anterior entopeduncular region morphology', 0.46774193548387094, 8.02346099791745, 1.9372426736073256, 'HP:0002060', 'Abnormal cerebral morphology'),
(729560, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0103102', 'abnormal anterior amygdala morphology', 0.42028985507246375, 8.02346099791745, 1.8363494384224073, 'HP:0002060', 'Abnormal cerebral morphology'),
(729561, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0101053', 'abnormal anterior hypothalamus', 0.4426229508196721, 6.667568321314008, 1.7179111633526845, 'HP:0100547', 'Abnormal forebrain morphology'),
(729562, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0101825', 'abnormal granule cell layer of the olfactory bulb morphology', 0.4027777777777778, 8.02346099791745, 1.7976851200440698, 'HP:0002060', 'Abnormal cerebral morphology'),
(729563, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0140838', 'abnormally necrotic anterior commissure', 0.4142857142857143, 8.02346099791745, 1.8231854734408677, 'HP:0002060', 'Abnormal cerebral morphology'),
(729564, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0140020', 'abnormally necrotic amygdala', 0.4084507042253521, 8.02346099791745, 1.810300608993995, 'HP:0002060', 'Abnormal cerebral morphology'),
(729565, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0100763', 'abnormal pretectum', 0.45, 6.667568321314008, 1.7321679319833003, 'HP:0100547', 'Abnormal forebrain morphology'),
(729566, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0101595', 'abnormal prosomere 4', 0.43548387096774194, 6.667568321314008, 1.704000722566664, 'HP:0100547', 'Abnormal forebrain morphology'),
(729567, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0115310', 'abnormally incomplete structure of forebrain', 0.42857142857142855, 6.667568321314008, 1.6904228111816126, 'HP:0100547', 'Abnormal forebrain morphology'),
(729568, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0140571', 'abnormally necrotic medial pallium', 0.4142857142857143, 8.02346099791745, 1.8231854734408677, 'HP:0002060', 'Abnormal cerebral morphology'),
(729569, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0100590', 'abnormal hypothalamus', 0.45, 6.667568321314008, 1.7321679319833003, 'HP:0100547', 'Abnormal forebrain morphology'),
(729570, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0128482', 'decreased size of the ventral pallium', 0.4027777777777778, 8.02346099791745, 1.7976851200440698, 'HP:0002060', 'Abnormal cerebral morphology'),
(729571, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0130244', 'increased size of the dorsal pallium', 0.4027777777777778, 8.02346099791745, 1.7976851200440698, 'HP:0002060', 'Abnormal cerebral morphology'),
(729572, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0101851', 'abnormal basal ganglion morphology', 0.4393939393939394, 8.02346099791745, 1.8776208710622537, 'HP:0002060', 'Abnormal cerebral morphology'),
(729573, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0101866', 'abnormal anterior entopeduncular nucleus morphology', 0.4142857142857143, 8.02346099791745, 1.8231854734408677, 'HP:0002060', 'Abnormal cerebral morphology'),
(729574, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0140421', 'abnormally necrotic anterior entopeduncular region', 0.4461538461538462, 8.02346099791745, 1.8920089808682852, 'HP:0002060', 'Abnormal cerebral morphology'),
(729575, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0100962', 'abnormal dorsal thalamus', 0.4426229508196721, 6.667568321314008, 1.7179111633526845, 'HP:0100547', 'Abnormal forebrain morphology'),
(729576, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0128766', 'decreased size of the dorsal pallium', 0.4027777777777778, 8.02346099791745, 1.7976851200440698, 'HP:0002060', 'Abnormal cerebral morphology'),
(729577, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0140554', 'abnormally necrotic central amygdala', 0.40476190476190477, 11.189682030596343, 2.1281816210991567, 'UPHENO:0088139', 'abnormal basal ganglion morphology'),
(729578, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0103200', 'abnormal prosomere 5 morphology', 0.4264705882352941, 8.02346099791745, 1.8498027277157947, 'HP:0002060', 'Abnormal cerebral morphology'),
(729579, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0101106', 'abnormal caudal tuberal region', 0.42857142857142855, 6.667568321314008, 1.6904228111816126, 'HP:0100547', 'Abnormal forebrain morphology'),
(729580, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0101986', 'abnormal amygdala morphology', 0.4393939393939394, 8.02346099791745, 1.8776208710622537, 'HP:0002060', 'Abnormal cerebral morphology'),
(729581, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0102978', 'abnormal prosomere 6 morphology', 0.4264705882352941, 8.02346099791745, 1.8498027277157947, 'HP:0002060', 'Abnormal cerebral morphology'),
(729582, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0101795', 'abnormal central amygdala morphology', 0.4358974358974359, 11.189682030596343, 2.20851844131865, 'UPHENO:0088139', 'abnormal basal ganglion morphology'),
(729583, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0102490', 'abnormal presumptive midbrain-hindbrain boundary morphology', 0.40384615384615385, 5.483278994082134, 1.4880863994491305, 'HP:0002011', 'Morphological central nervous system abnormality'),
(729584, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0101123', 'abnormal third ventricle', 0.43548387096774194, 6.667568321314008, 1.704000722566664, 'HP:0100547', 'Abnormal forebrain morphology'),
(729585, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0101970', 'abnormal lateral ganglionic eminence morphology', 0.4393939393939394, 8.02346099791745, 1.8776208710622537, 'HP:0002060', 'Abnormal cerebral morphology'),
(729586, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0103178', 'abnormal dorsal pallium morphology', 0.4461538461538462, 8.02346099791745, 1.8920089808682852, 'HP:0002060', 'Abnormal cerebral morphology'),
(729587, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0101184', 'abnormal suprachiasmatic nucleus', 0.421875, 6.667568321314008, 1.677164388351466, 'HP:0100547', 'Abnormal forebrain morphology'),
(729588, 'HP:0012752', 'Focal T2 hypointense basal ganglia lesion', 'XPO:0102361', 'abnormal thalamus morphology', 0.40298507462686567, 6.667568321314008, 1.639185931352649, 'HP:0100547', 'Abnormal forebrain morphology'),
(729589, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0131719', 'abnormal activation of meiosis', 0.42857142857142855, 3.334430194052109, 1.195425243056469, 'UPHENO:0049587', 'abnormal biological_process'),
(729590, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0141892', 'abnormal inositol metabolic process', 0.5, 4.758907843651163, 1.5425478669479211, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(729591, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0101297', 'abnormal barrier cell', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(729592, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0141744', 'abnormal chemical homeostasis', 0.47619047619047616, 9.069942786322247, 2.078225294437339, 'UPHENO:0049904', 'abnormal homeostatic process'),
(729593, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0141768', 'abnormal tissue homeostasis', 0.4583333333333333, 10.518562886125473, 2.1956793913215504, 'UPHENO:0088229', 'abnormal multicellular organismal-level homeostasis'),
(729594, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0141760', 'abnormal multicellular organismal homeostasis', 0.55, 10.518562886125473, 2.405246263352052, 'UPHENO:0088229', 'abnormal multicellular organismal-level homeostasis'),
(729595, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0141841', 'abnormality of whole organism mass', 0.4074074074074074, 3.334430194052109, 1.1655348817344542, 'UPHENO:0049587', 'abnormal biological_process'),
(729596, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0141874', 'abnormal creatinine metabolic process', 0.41379310344827586, 4.758907843651163, 1.4032830240720355, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(729597, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0141747', 'abnormal epidermal stem cell homeostasis', 0.4583333333333333, 10.518562886125473, 2.1956793913215504, 'UPHENO:0088229', 'abnormal multicellular organismal-level homeostasis'),
(729598, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0141872', 'abnormal cholesterol metabolic process', 0.42857142857142855, 4.758907843651163, 1.4281218200816608, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(729599, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0131714', 'abnormal establishment of tissue polarity', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(729600, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0141272', 'absent surface breathing', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(729601, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0141791', 'abnormal primary metabolic process', 0.5454545454545454, 4.758907843651163, 1.6111387012665346, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(729602, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0141860', 'abnormal malate-aspartate shuttle', 0.5217391304347826, 4.758907843651163, 1.575724734896874, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(729603, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0141900', 'abnormal mannose metabolic process', 0.4444444444444444, 4.758907843651163, 1.4543280760316257, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(729604, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0141866', 'abnormal dicarboxylic acid metabolic process', 0.42857142857142855, 4.758907843651163, 1.4281218200816608, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(729605, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0141797', 'abnormal hydrogen metabolic process', 0.5454545454545454, 4.758907843651163, 1.6111387012665346, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(729606, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0141751', 'abnormal hepatocyte homeostasis', 0.4583333333333333, 10.518562886125473, 2.1956793913215504, 'UPHENO:0088229', 'abnormal multicellular organismal-level homeostasis'),
(729607, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0131975', 'abnormal development of anatomical line', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(729608, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0141910', 'abnormal D-ribose metabolic process', 0.4444444444444444, 4.758907843651163, 1.4543280760316257, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(729609, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0141884', 'abnormal phosphagen metabolic process', 0.4444444444444444, 4.758907843651163, 1.4543280760316257, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(729610, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0131728', 'abnormal regulation of cell size', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(729611, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0141850', 'abnormal galactose metabolic process', 0.4444444444444444, 4.758907843651163, 1.4543280760316257, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(729612, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0141767', 'abnormal temperature homeostasis', 0.7272727272727273, 13.627087342903641, 3.1481119701588116, 'HP:0004370', 'Abnormality of temperature regulation'),
(729613, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0141724', 'abnormal prevention of polyspermy', 0.42857142857142855, 3.334430194052109, 1.195425243056469, 'UPHENO:0049587', 'abnormal biological_process'),
(729614, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0141881', 'abnormal fructose metabolic process', 0.4444444444444444, 4.758907843651163, 1.4543280760316257, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(729615, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0116429', 'abnormal behavior', 0.42857142857142855, 3.334430194052109, 1.195425243056469, 'UPHENO:0049587', 'abnormal biological_process'),
(729616, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0141754', 'abnormal homeostatic process', 0.5263157894736842, 9.069942786322247, 2.1848693549190394, 'UPHENO:0049904', 'abnormal homeostatic process'),
(729617, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0100004', 'abnormal cell', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(729618, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0131705', 'abnormal chemotaxis', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(729619, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0100026', 'abnormal germ cell', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(729620, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0141771', 'abnormal urea homeostasis', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(729621, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0131722', 'abnormal determination of left/right symmetry', 0.42857142857142855, 3.334430194052109, 1.195425243056469, 'UPHENO:0049587', 'abnormal biological_process'),
(729622, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0100108', 'abnormal cell part', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(729623, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0141785', 'abnormal thyroid hormone metabolic process', 0.41379310344827586, 4.758907843651163, 1.4032830240720355, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(729624, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0100289', 'abnormal chondroblast', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(729625, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0100802', 'abnormal exocrine cell', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(729626, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0141758', 'abnormal leukocyte homeostasis', 0.4583333333333333, 10.518562886125473, 2.1956793913215504, 'UPHENO:0088229', 'abnormal multicellular organismal-level homeostasis'),
(729627, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0100691', 'abnormal keratin accumulating cell', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(729628, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0133340', 'abnormal cell adhesion', 0.42857142857142855, 3.334430194052109, 1.195425243056469, 'UPHENO:0049587', 'abnormal biological_process'),
(729629, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0101132', 'abnormal apoptotic cell', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(729630, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0141276', 'decreased surface breathing', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(729631, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0116494', 'absent biological process', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(729632, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0100638', 'abnormal polar body', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(729633, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0141795', 'abnormal glycosylation', 0.5, 4.758907843651163, 1.5425478669479211, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(729634, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0141877', 'abnormal 2-deoxyribose 1-phosphate metabolic process', 0.48, 4.758907843651163, 1.5113820711364014, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(729635, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0141880', 'abnormal ethanolamine metabolic process', 0.46153846153846156, 4.758907843651163, 1.482032052542075, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(729636, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:00000000', 'Xenopus phenotype', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(729637, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0131715', 'abnormal fibroblast growth factor receptor signaling pathway', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(729638, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0141789', 'abnormal hormone catabolic process', 0.46153846153846156, 4.758907843651163, 1.482032052542075, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(729639, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0131725', 'abnormal phosphorylation of RNA polymerase II C-terminal domain', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(729640, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0141883', 'abnormal glycerol metabolic process', 0.4444444444444444, 4.758907843651163, 1.4543280760316257, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(729641, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0141782', 'abnormal methylation', 0.5454545454545454, 4.758907843651163, 1.6111387012665346, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(729642, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0141911', 'abnormal ribose phosphate metabolic process', 0.48, 4.758907843651163, 1.5113820711364014, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(729643, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0101448', 'abnormal myelin accumulating cell', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(729644, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0141899', 'abnormal mandelate metabolic process', 0.41379310344827586, 4.758907843651163, 1.4032830240720355, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(729645, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0141781', 'abnormal secondary metabolic process', 0.5454545454545454, 4.758907843651163, 1.6111387012665346, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(729646, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0131469', 'abnormal heart process', 0.45, 3.334430194052109, 1.2249463609984925, 'UPHENO:0049587', 'abnormal biological_process'),
(729647, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0141742', 'abnormal cellular homeostasis', 0.4166666666666667, 9.069942786322247, 1.9440017560779799, 'UPHENO:0049904', 'abnormal homeostatic process'),
(729648, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0100006', 'abnormal anatomical structure', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(729649, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0141915', 'abnormal taurine metabolic process', 0.41379310344827586, 4.758907843651163, 1.4032830240720355, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(729650, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0100285', 'abnormal progenitor cell', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(729651, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0141794', 'abnormal prosthetic group metabolic process', 0.5454545454545454, 4.758907843651163, 1.6111387012665346, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(729652, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0101435', 'abnormal paracrine cell', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(729653, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0100172', 'abnormal stem cell', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(729654, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0100704', 'abnormal Merkel cell', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(729655, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0100533', 'abnormal melanoblast', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(729656, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0141775', 'abnormal nitrogen compound metabolic process', 0.5454545454545454, 4.758907843651163, 1.6111387012665346, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(729657, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0101467', 'abnormal alkali secreting cell', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(729658, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0141852', 'abnormal glucose metabolic process', 0.4444444444444444, 4.758907843651163, 1.4543280760316257, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(729659, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0141975', 'abnormal cilium motility', 0.42857142857142855, 3.334430194052109, 1.195425243056469, 'UPHENO:0049587', 'abnormal biological_process'),
(729660, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0101373', 'abnormal oxygen accumulating cell', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(729661, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0101535', 'abnormal absorptive cell', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(729662, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0141854', 'abnormal glutathione metabolic process', 0.4444444444444444, 4.758907843651163, 1.4543280760316257, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(729663, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0141798', 'abnormal lipid metabolic process', 0.5, 4.758907843651163, 1.5425478669479211, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(729664, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0100653', 'abnormal myoblast', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(729665, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0141762', 'abnormal multicellular organismal water homeostasis', 0.5769230769230769, 10.518562886125473, 2.463412605527622, 'UPHENO:0088229', 'abnormal multicellular organismal-level homeostasis'),
(729666, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0141753', 'abnormal homeostasis of number of cells', 0.5, 10.518562886125473, 2.2933123300289338, 'UPHENO:0088229', 'abnormal multicellular organismal-level homeostasis'),
(729667, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0141903', 'abnormal inositol phosphate metabolic process', 0.4444444444444444, 4.758907843651163, 1.4543280760316257, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(729668, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0141267', 'abnormal resting posture', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(729669, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0100481', 'abnormal anatomical line', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(729670, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0131744', 'abnormal apical constriction', 0.42857142857142855, 3.334430194052109, 1.195425243056469, 'UPHENO:0049587', 'abnormal biological_process'),
(729671, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0101326', 'abnormal cementoblast', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(729672, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0131765', 'abnormal development of anatomical region', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(729673, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0141745', 'abnormal creatinine homeostasis', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(729674, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0131703', 'abnormal cell division', 0.42857142857142855, 3.334430194052109, 1.195425243056469, 'UPHENO:0049587', 'abnormal biological_process'),
(729675, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0141898', 'abnormal maltose metabolic process', 0.48, 4.758907843651163, 1.5113820711364014, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(729676, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0141908', 'abnormal pyridine metabolic process', 0.4444444444444444, 4.758907843651163, 1.4543280760316257, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(729677, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0131721', 'abnormal nodal signaling pathway', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(729678, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0141755', 'abnormal intestinal stem cell homeostasis', 0.4583333333333333, 10.518562886125473, 2.1956793913215504, 'UPHENO:0088229', 'abnormal multicellular organismal-level homeostasis'),
(729679, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0141792', 'abnormal small molecule metabolic process', 0.5454545454545454, 4.758907843651163, 1.6111387012665346, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(729680, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0141904', 'abnormal glucosamine metabolic process', 0.5454545454545454, 4.758907843651163, 1.6111387012665346, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(729681, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0131711', 'abnormal establishment of cell polarity', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(729682, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0100337', 'abnormal zygote', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(729683, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0116434', 'abnormal biological process', 0.5, 3.334430194052109, 1.2912068374300278, 'UPHENO:0049587', 'abnormal biological_process'),
(729684, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0141759', 'abnormal lipid homeostasis', 0.43478260869565216, 9.069942786322247, 1.9858130288014273, 'UPHENO:0049904', 'abnormal homeostatic process'),
(729685, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0141907', 'abnormal putrescine metabolic process', 0.5, 4.758907843651163, 1.5425478669479211, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(729686, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0131723', 'abnormal pathway-restricted SMAD protein phosphorylation', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(729687, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0131738', 'abnormal Wnt signaling pathway', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(729688, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0131691', 'abnormal molecular function', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(729689, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0141784', 'abnormal cellular hormone metabolic process', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(729690, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0116433', 'abnormal axis specification', 0.42857142857142855, 3.334430194052109, 1.195425243056469, 'UPHENO:0049587', 'abnormal biological_process'),
(729691, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0141796', 'abnormal demethylation', 0.5454545454545454, 4.758907843651163, 1.6111387012665346, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(729692, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0141770', 'abnormal urate homeostasis', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(729693, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0131729', 'abnormal regulation of growth rate', 0.45, 3.334430194052109, 1.2249463609984925, 'UPHENO:0049587', 'abnormal biological_process'),
(729694, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0141863', 'abnormal lactate metabolic process', 0.41379310344827586, 4.758907843651163, 1.4032830240720355, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(729695, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0131798', 'abnormal development of anatomical space', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(729696, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0100754', 'abnormal electrically active cell', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(729697, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0101241', 'abnormal nucleate erythrocyte', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(729698, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0133397', 'abnormal insulin receptor signaling pathway', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(729699, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0141748', 'abnormal gas homeostasis', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(729700, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0131730', 'abnormal regulation of protein folding', 0.45, 3.334430194052109, 1.2249463609984925, 'UPHENO:0049587', 'abnormal biological_process'),
(729701, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0101004', 'abnormal acid secreting cell', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(729702, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0141790', 'abnormal cellular metabolic process', 0.5217391304347826, 4.758907843651163, 1.575724734896874, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(729703, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0131740', 'abnormal detection of nodal flow', 0.42857142857142855, 3.334430194052109, 1.195425243056469, 'UPHENO:0049587', 'abnormal biological_process'),
(729704, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0141746', 'abnormal energy homeostasis', 0.5, 10.518562886125473, 2.2933123300289338, 'UPHENO:0088229', 'abnormal multicellular organismal-level homeostasis'),
(729705, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0101333', 'abnormal barrier epithelial cell', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(729706, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0141750', 'abnormal hematopoietic stem cell homeostasis', 0.4583333333333333, 10.518562886125473, 2.1956793913215504, 'UPHENO:0088229', 'abnormal multicellular organismal-level homeostasis'),
(729707, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0141737', 'abnormal carbohydrate homeostasis', 0.43478260869565216, 9.069942786322247, 1.9858130288014273, 'UPHENO:0049904', 'abnormal homeostatic process'),
(729708, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0141265', 'abnormal escape behavior', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(729709, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0141772', 'abnormal water homeostasis', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(729710, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0141920', 'abnormal urea metabolic process', 0.41379310344827586, 4.758907843651163, 1.4032830240720355, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(729711, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0141757', 'abnormal ion homeostasis', 0.43478260869565216, 9.069942786322247, 1.9858130288014273, 'UPHENO:0049904', 'abnormal homeostatic process'),
(729712, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0100549', 'abnormal mitotic cell', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(729713, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0141859', 'abnormal lactose catabolic process', 0.4444444444444444, 4.758907843651163, 1.4543280760316257, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(729714, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0141271', 'increased surface breathing', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(729715, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0100477', 'abnormal pericyte', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(729716, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0100081', 'abnormal anatomical entity in vitro', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(729717, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0131760', 'abnormal development of anatomical structure', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(729718, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0141864', 'abnormal 5-methylcytosine metabolic process', 0.4444444444444444, 4.758907843651163, 1.4543280760316257, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(729719, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0141761', 'abnormal multicellular organismal iron ion homeostasis', 0.4074074074074074, 10.518562886125473, 2.070106382553359, 'UPHENO:0088229', 'abnormal multicellular organismal-level homeostasis'),
(729720, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0100715', 'abnormal ciliated cell', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(729721, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0100344', 'abnormal portion of organism substance', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(729722, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0141783', 'abnormal collagen metabolic process', 0.5454545454545454, 4.758907843651163, 1.6111387012665346, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(729723, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0141871', 'abnormal cadaverine transport', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(729724, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0132054', 'abnormal development of portion of organism substance', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(729725, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0141264', 'abnormal schooling behavior', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(729726, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0141787', 'abnormal hormone metabolic process', 0.5454545454545454, 4.758907843651163, 1.6111387012665346, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(729727, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0141736', 'abnormal anatomical structure homeostasis', 0.5, 10.518562886125473, 2.2933123300289338, 'UPHENO:0088229', 'abnormal multicellular organismal-level homeostasis'),
(729728, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0141856', 'abnormal glycerolipid metabolic process', 0.41379310344827586, 4.758907843651163, 1.4032830240720355, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(729729, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0141776', 'abnormal metabolic process', 0.6, 4.758907843651163, 1.6897765255177082, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(729730, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0133403', 'abnormal developmental process', 0.45, 3.334430194052109, 1.2249463609984925, 'UPHENO:0049587', 'abnormal biological_process'),
(729731, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0101237', 'abnormal mucus secreting cell', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(729732, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0141263', 'abnormal visually guided collision avoidance behavior', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(729733, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0141777', 'abnormal catabolic process', 0.5454545454545454, 4.758907843651163, 1.6111387012665346, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(729734, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0141738', 'abnormal carbon dioxide homeostasis', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(729735, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0141749', 'abnormal germ-line stem-cell niche homeostasis', 0.4583333333333333, 10.518562886125473, 2.1956793913215504, 'UPHENO:0088229', 'abnormal multicellular organismal-level homeostasis'),
(729736, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0100852', 'abnormal interdigital region', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(729737, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0131470', 'abnormal heart contraction', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(729738, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0141764', 'abnormal myeloid cell homeostasis', 0.4583333333333333, 10.518562886125473, 2.1956793913215504, 'UPHENO:0088229', 'abnormal multicellular organismal-level homeostasis'),
(729739, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0141266', 'abnormal surface breathing', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(729740, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0141788', 'abnormal hormone biosynthetic process', 0.46153846153846156, 4.758907843651163, 1.482032052542075, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(729741, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0131700', 'abnormal BMP signaling pathway', 0.4090909090909091, 3.334430194052109, 1.1679405290445888, 'UPHENO:0049587', 'abnormal biological_process'),
(729742, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0141778', 'abnormal biosynthetic process', 0.5454545454545454, 4.758907843651163, 1.6111387012665346, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(729743, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0141743', 'abnormal chemical homeostasis within a tissue', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(729744, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0141786', 'abnormal pigment metabolic process', 0.5454545454545454, 4.758907843651163, 1.6111387012665346, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(729745, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0131745', 'abnormal axis elongation', 0.44, 3.334430194052109, 1.2112593798947144, 'UPHENO:0049587', 'abnormal biological_process'),
(729746, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0131694', 'abnormal RNA polymerase II activity', 0.4230769230769231, 4.758907843651163, 1.418937661667548, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(729747, 'HP:0004370', 'Abnormality of temperature regulation', 'XPO:0100791', 'abnormal multiciliated cell precursor', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(729748, 'HP:0034564', 'Kidney teratoma', 'XPO:0100501', 'abnormal urogenital system', 0.41935483870967744, 5.4478002382576385, 1.5114765596055648, 'HP:0000119', 'Abnormality of the genitourinary system'),
(729749, 'HP:0034564', 'Kidney teratoma', 'XPO:0100120', 'abnormal genital system', 0.46875, 6.57633172329375, 1.755749268914541, 'UPHENO:0003055', 'abnormal reproductive system'),
(729750, 'HP:0034564', 'Kidney teratoma', 'XPO:0101493', 'abnormal fat body', 0.4166666666666667, 6.57633172329375, 1.655336285483727, 'UPHENO:0003055', 'abnormal reproductive system'),
(729751, 'HP:0034564', 'Kidney teratoma', 'XPO:0100037', 'abnormal gonad', 0.40540540540540543, 6.57633172329375, 1.632813653900019, 'UPHENO:0003055', 'abnormal reproductive system'),
(729752, 'HP:0034564', 'Kidney teratoma', 'XPO:0100316', 'abnormal gamete', 0.40540540540540543, 6.57633172329375, 1.632813653900019, 'UPHENO:0003055', 'abnormal reproductive system'),
(729753, 'HP:0012878', 'Retarded ejaculation', 'XPO:0102397', 'abnormal male genitalia morphology', 0.46153846153846156, 8.414388317771037, 1.9706759852830318, 'HP:0010461', 'Abnormality of the male genitalia'),
(729754, 'HP:0012878', 'Retarded ejaculation', 'XPO:0139867', 'abnormally necrotic genital system', 0.41509433962264153, 7.005035523447265, 1.705212771075354, 'HP:0012243', 'Abnormal reproductive system morphology'),
(729755, 'HP:0012878', 'Retarded ejaculation', 'XPO:0101262', 'abnormal oviduct', 0.4230769230769231, 7.005035523447265, 1.7215309684419309, 'HP:0012243', 'Abnormal reproductive system morphology'),
(729756, 'HP:0012878', 'Retarded ejaculation', 'XPO:0102864', 'abnormal female genitalia morphology', 0.4074074074074074, 7.005035523447265, 1.689349981917436, 'UPHENO:0020950', 'abnormal reproductive system morphology'),
(729757, 'HP:0012878', 'Retarded ejaculation', 'XPO:0139866', 'abnormally necrotic male genitalia', 0.41379310344827586, 8.414388317771037, 1.8659624475399805, 'HP:0010461', 'Abnormality of the male genitalia'),
(729758, 'HP:0012878', 'Retarded ejaculation', 'XPO:0101372', 'abnormal seminiferous tubule', 0.4067796610169492, 8.414388317771037, 1.8500816272715859, 'HP:0010461', 'Abnormality of the male genitalia'),
(729759, 'HP:0012878', 'Retarded ejaculation', 'XPO:0100414', 'abnormal testis', 0.42857142857142855, 8.414388317771037, 1.8989908956869364, 'HP:0010461', 'Abnormality of the male genitalia'),
(729760, 'HP:0012878', 'Retarded ejaculation', 'XPO:0101232', 'abnormal female genitalia', 0.4583333333333333, 7.005035523447265, 1.7918262420167856, 'UPHENO:0020950', 'abnormal reproductive system morphology'),
(729761, 'HP:0012878', 'Retarded ejaculation', 'XPO:0100765', 'abnormal male genitalia', 0.5217391304347826, 8.414388317771037, 2.095260280741859, 'HP:0010461', 'Abnormality of the male genitalia'),
(729762, 'HP:0012878', 'Retarded ejaculation', 'XPO:0126762', 'abnormally localised male genitalia', 0.43636363636363634, 8.414388317771037, 1.916176683951214, 'HP:0010461', 'Abnormality of the male genitalia'),
(729763, 'HP:0012878', 'Retarded ejaculation', 'XPO:0101752', 'abnormal genital system morphology', 0.4583333333333333, 7.005035523447265, 1.7918262420167856, 'UPHENO:0020950', 'abnormal reproductive system morphology'),
(729764, 'HP:0012878', 'Retarded ejaculation', 'XPO:0102270', 'abnormal polar body morphology', 0.41509433962264153, 7.005035523447265, 1.705212771075354, 'UPHENO:0020950', 'abnormal reproductive system morphology'),
(729765, 'HP:0012878', 'Retarded ejaculation', 'XPO:0125139', 'absent male genitalia', 0.42857142857142855, 8.414388317771037, 1.8989908956869364, 'HP:0010461', 'Abnormality of the male genitalia'),
(729766, 'HP:0002864', 'Paraganglioma of head and neck', 'XPO:0101952', 'abnormal lateral line morphology', 0.40816326530612246, 7.318748312764234, 1.7283646054266224, 'HP:0000759', 'Abnormal peripheral nervous system morphology'),
(729767, 'HP:0002864', 'Paraganglioma of head and neck', 'XPO:0100167', 'abnormal nerve', 0.45454545454545453, 7.318748312764234, 1.823925376359789, 'HP:0000759', 'Abnormal peripheral nervous system morphology'),
(729768, 'HP:0002864', 'Paraganglioma of head and neck', 'XPO:0100114', 'abnormal peripheral nervous system', 0.40540540540540543, 6.642668884102504, 1.6410282971153933, 'HP:0410008', 'Abnormality of the peripheral nervous system'),
(729769, 'HP:0002864', 'Paraganglioma of head and neck', 'XPO:0101030', 'abnormal spinal nerve', 0.43478260869565216, 7.318748312764234, 1.783834208610917, 'HP:0000759', 'Abnormal peripheral nervous system morphology'),
(729770, 'HP:0002864', 'Paraganglioma of head and neck', 'XPO:0101746', 'abnormal peripheral nervous system morphology', 0.4444444444444444, 7.318748312764234, 1.8035456822313138, 'HP:0000759', 'Abnormal peripheral nervous system morphology'),
(729771, 'HP:0002864', 'Paraganglioma of head and neck', 'XPO:0100635', 'abnormal sympathetic chain', 0.4166666666666667, 7.318748312764234, 1.7462755978515432, 'HP:0000759', 'Abnormal peripheral nervous system morphology'),
(729772, 'HP:0002864', 'Paraganglioma of head and neck', 'XPO:0101204', 'abnormal peripheral nerve', 0.45454545454545453, 7.318748312764234, 1.823925376359789, 'HP:0000759', 'Abnormal peripheral nervous system morphology'),
(729773, 'HP:0002864', 'Paraganglioma of head and neck', 'XPO:0102366', 'abnormal lateral line system morphology', 0.425531914893617, 7.318748312764234, 1.7647552193307132, 'HP:0000759', 'Abnormal peripheral nervous system morphology'),
(729774, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0101136', 'abnormal ooplasm', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(729775, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100585', 'abnormal elastica externa', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(729776, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0101450', 'abnormal myeloid cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(729777, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100376', 'abnormal animal pole', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(729778, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0101500', 'abnormal endodermal cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(729779, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0141791', 'abnormal primary metabolic process', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(729780, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0131687', 'abnormal astral microtubule', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(729781, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100386', 'abnormal limb', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(729782, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0107271', 'abnormal apical region', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(729783, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0107285', 'abnormal flexural organ', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(729784, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0131666', 'abnormal adherens junction', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(729785, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0107276', 'abnormal dorsal region', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(729786, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100954', 'abnormal neural progenitor cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(729787, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0126318', 'abnormally localised cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(729788, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100189', 'abnormal enteroendocrine cell', 0.52, 6.2194654996189955, 1.7983664976310803, 'UPHENO:0003116', 'abnormal endocrine system'),
(729789, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0142054', 'abnormal digestive tract', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(729790, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0101402', 'abnormal oropharyngeal papilla', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(729791, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0101040', 'abnormal axial mesoderm', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(729792, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0131667', 'abnormal actin cytoskeleton', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(729793, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0141892', 'abnormal inositol metabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(729794, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100014', 'abnormal tissue', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(729795, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0131691', 'abnormal molecular function', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(729796, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100203', 'abnormal endocrine cell', 0.5416666666666666, 6.2194654996189955, 1.835450120713433, 'UPHENO:0003116', 'abnormal endocrine system'),
(729797, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100009', 'abnormal multi-tissue structure', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(729798, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100151', 'abnormal primordium', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(729799, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0101362', 'abnormal vegetal cortex', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(729800, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100384', 'abnormal amputated tissue', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(729801, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100423', 'abnormal process', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(729802, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100842', 'abnormal left-dorsal blastomere', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(729803, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0131669', 'abnormal Roux spot', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(729804, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0141263', 'abnormal visually guided collision avoidance behavior', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(729805, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0101451', 'abnormal dorsal lymph space', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(729806, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100969', 'abnormal disaggregated/reaggregated ectoderm treated with activin', 0.5294117647058824, 1.706362323152461, 0.9504568842024205, 'UPHENO:0002536', 'abnormal anatomical entity'),
(729807, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100449', 'abnormal lymphocyte', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(729808, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100862', 'abnormal blastomere V1', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(729809, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0101389', 'abnormal wedge region', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(729810, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100393', 'abnormal involuting marginal zone', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(729811, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100511', 'abnormal stylopod', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(729812, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0101396', 'abnormal apical epithelial cap', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(729813, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100557', 'abnormal prime meridian', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(729814, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0101480', 'abnormal stage V oocyte', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(729815, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100332', 'abnormal germinal granule', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(729816, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100394', 'abnormal marginal zone', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(729817, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0101573', 'abnormal peripheral vegetal yolk mass', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(729818, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0101535', 'abnormal absorptive cell', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(729819, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100187', 'abnormal regenerating limb', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(729820, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0101560', 'abnormal compound organ component', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(729821, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100133', 'abnormal solid compound organ', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(729822, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100277', 'abnormal blastocoel', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(729823, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100864', 'abnormal dorsolateral ascending neuron', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(729824, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0141772', 'abnormal water homeostasis', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(729825, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0107264', 'abnormal anterior side', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(729826, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100429', 'abnormal spermatid', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(729827, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100274', 'abnormal sensory system', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(729828, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100721', 'abnormal centromere', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(729829, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100523', 'abnormal midgut', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(729830, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0141748', 'abnormal gas homeostasis', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(729831, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0125191', 'absent endocrine system', 0.41935483870967744, 6.2194654996189955, 1.6149807898093176, 'UPHENO:0003116', 'abnormal endocrine system'),
(729832, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0107268', 'abnormal left side', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(729833, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100415', 'abnormal secretory epithelial cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(729834, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100028', 'abnormal anatomical cluster', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(729835, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0107258', 'abnormal anatomical axis', 0.5294117647058824, 1.706362323152461, 0.9504568842024205, 'UPHENO:0002536', 'abnormal anatomical entity'),
(729836, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0141860', 'abnormal malate-aspartate shuttle', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(729837, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100867', 'abnormal apical mesenchyme', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(729838, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100872', 'abnormal neuroendocrine cell', 0.52, 6.2194654996189955, 1.7983664976310803, 'UPHENO:0003116', 'abnormal endocrine system'),
(729839, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0101228', 'abnormal mesenchymal stem cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(729840, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100890', 'abnormal pharyngeal cavity', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(729841, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0107326', 'abnormal regenerating pelvic girdle', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(729842, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100587', 'abnormal vestibuloauditory system', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(729843, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0101221', 'abnormal larval immune system', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(729844, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100251', 'abnormal proteinaceous extracellular matrix', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(729845, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0141714', 'abnormal anterior notochord', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(729846, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100907', 'abnormal cytoplasm', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(729847, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0101460', 'abnormal fibrocellular pad', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(729848, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100856', 'abnormal simple organ', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(729849, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0101976', 'abnormal portion of organism substance morphology', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(729850, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0101472', 'abnormal zygote cortex', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(729851, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100205', 'abnormal limb segment', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(729852, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100337', 'abnormal zygote', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(729853, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0141776', 'abnormal metabolic process', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(729854, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0141715', 'abnormal septum', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(729855, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100545', 'abnormal male organism', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(729856, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0101333', 'abnormal barrier epithelial cell', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(729857, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0141265', 'abnormal escape behavior', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(729858, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0141797', 'abnormal hydrogen metabolic process', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(729859, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100687', 'abnormal periotic region', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(729860, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0107284', 'abnormal migrating myoblast', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(729861, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100537', 'abnormal medium cavity', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(729862, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0128000', 'absent behavior', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(729863, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0101224', 'abnormal dorsal involuting marginal zone', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(729864, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0141315', 'abnormal anatomical region', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(729865, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0101149', 'abnormal amputated limb', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(729866, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0101162', 'abnormal stromal cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(729867, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100665', 'abnormal egg jelly', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(729868, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0107269', 'abnormal right side', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(729869, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100653', 'abnormal myoblast', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(729870, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100484', 'abnormal cement gland primordium', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(729871, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0101547', 'abnormal lampbrush chromosome', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(729872, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100378', 'abnormal perichondrium', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(729873, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0101463', 'abnormal right-ventral blastomere', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(729874, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0101074', 'abnormal germinal vesicle', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(729875, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0115362', 'abnormally decreased adhesivity of prechordal plate', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(729876, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100377', 'abnormal connective tissue', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(729877, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100296', 'abnormal tail region', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(729878, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0141904', 'abnormal glucosamine metabolic process', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(729879, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100162', 'abnormal presumptive rhombomere', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(729880, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100573', 'abnormal extraembryonic structure', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(729881, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100308', 'abnormal early embryonic cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(729882, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0101133', 'abnormal motor neuron', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(729883, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0107270', 'abnormal proximal-distal axis', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(729884, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100444', 'abnormal cement gland', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(729885, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0115391', 'abnormally undifferentiated alimentary system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(729886, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100887', 'abnormal right-dorsal blastomere', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(729887, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100477', 'abnormal pericyte', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(729888, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0101518', 'abnormal B cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(729889, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100515', 'abnormal somatic stem cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(729890, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0141266', 'abnormal surface breathing', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(729891, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0131729', 'abnormal regulation of growth rate', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(729892, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100417', 'abnormal dense regular connective tissue', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(729893, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0141787', 'abnormal hormone metabolic process', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(729894, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100546', 'abnormal whole organism', 0.5294117647058824, 1.706362323152461, 0.9504568842024205, 'UPHENO:0002536', 'abnormal anatomical entity'),
(729895, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0115505', 'dead whole organism', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(729896, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100643', 'abnormal thoracic region', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(729897, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100728', 'abnormal cell condensation', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(729898, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100175', 'abnormal migrating neuroblast', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(729899, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0101406', 'abnormal cleavage furrow', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(729900, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0141783', 'abnormal collagen metabolic process', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(729901, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100581', 'abnormal immune system', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(729902, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0101168', 'abnormal circulating cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(729903, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0133403', 'abnormal developmental process', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(729904, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100722', 'abnormal barbel', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(729905, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100688', 'abnormal adipose tissue', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(729906, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100481', 'abnormal anatomical line', 0.5625, 1.706362323152461, 0.9797085315405084, 'UPHENO:0002536', 'abnormal anatomical entity'),
(729907, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0101424', 'abnormal coelomic epithelium', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(729908, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100273', 'abnormal visual system', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(729909, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100674', 'abnormal secondary oogonium', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(729910, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0141798', 'abnormal lipid metabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(729911, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100750', 'abnormal regenerating fin', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(729912, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100917', 'abnormal stage III oocyte', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(729913, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0101113', 'abnormal stage IV oocyte', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(729914, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100640', 'abnormal notochordal sheath', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(729915, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0101263', 'abnormal blastocoel floor', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(729916, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100784', 'abnormal left blastomere', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(729917, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100135', 'abnormal surface structure', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(729918, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100868', 'abnormal transporting epithelium', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(729919, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100344', 'abnormal portion of organism substance', 0.5625, 1.706362323152461, 0.9797085315405084, 'UPHENO:0002536', 'abnormal anatomical entity'),
(729920, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100427', 'abnormal olfactory system', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(729921, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0141754', 'abnormal homeostatic process', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(729922, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0124719', 'absent anatomical structure', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(729923, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100760', 'abnormal Stirnorgan', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(729924, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100486', 'abnormal oral evagination', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(729925, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0101200', 'abnormal joint region', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(729926, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100846', 'abnormal hindlimb', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(729927, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0101543', 'abnormal external gill', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(729928, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0101569', 'abnormal activin-induced ectoderm', 0.5294117647058824, 1.706362323152461, 0.9504568842024205, 'UPHENO:0002536', 'abnormal anatomical entity'),
(729929, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0141264', 'abnormal schooling behavior', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(729930, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0107253', 'abnormal enteric nervous system', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(729931, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0101461', 'abnormal sperm entry point', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(729932, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100989', 'abnormal right blastomere', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(729933, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0101083', 'abnormal T cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(729934, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100702', 'abnormal glial cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(729935, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0116091', 'abnormally increased variability of size of cell in endoderm', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(729936, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100458', 'abnormal autopod', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(729937, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100976', 'abnormal multiciliated cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(729938, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0141743', 'abnormal chemical homeostasis within a tissue', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(729939, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0115574', 'abnormal variability of size of hindlimb', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(729940, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100781', 'abnormal presumptive ectoderm', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(729941, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0101057', 'abnormal vegetal pole', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(729942, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0127618', 'abnormally localised parathyroid', 0.4117647058823529, 12.404694921567193, 2.2600476888639833, 'HP:0000828', 'Abnormality of the parathyroid gland'),
(729943, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100533', 'abnormal melanoblast', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(729944, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0101448', 'abnormal myelin accumulating cell', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(729945, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100638', 'abnormal polar body', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(729946, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0101174', 'abnormal articular system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(729947, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100999', 'abnormal serous membrane', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(729948, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0101176', 'abnormal non-ciliated epithelial cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(729949, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100402', 'abnormal zeugopod', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(729950, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0131730', 'abnormal regulation of protein folding', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(729951, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100062', 'abnormal anatomical space', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(729952, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100103', 'abnormal trunk', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(729953, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:00000000', 'Xenopus phenotype', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(729954, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0101368', 'abnormal regenerating eye', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(729955, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0115473', 'abnormally delayed phase of Mullerian duct', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(729956, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100900', 'abnormal angioblast', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(729957, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0101373', 'abnormal oxygen accumulating cell', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(729958, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100800', 'abnormal ventral marginal zone', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(729959, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0141795', 'abnormal glycosylation', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(729960, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100403', 'abnormal forelimb', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(729961, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100398', 'abnormal vegetal blastomere', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(729962, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100158', 'abnormal neuromere', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(729963, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0101533', 'abnormal simple cuboidal epithelium', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(729964, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100627', 'abnormal pharyngeal region', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(729965, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100827', 'abnormal atypical epithelium', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(729966, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0101638', 'abnormal anatomical structure morphology', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(729967, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100026', 'abnormal germ cell', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(729968, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0101467', 'abnormal alkali secreting cell', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(729969, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0101010', 'abnormal dorsal marginal zone', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(729970, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100802', 'abnormal exocrine cell', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(729971, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100006', 'abnormal anatomical structure', 0.5625, 1.706362323152461, 0.9797085315405084, 'UPHENO:0002536', 'abnormal anatomical entity'),
(729972, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100610', 'abnormal appendage', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(729973, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100626', 'abnormal primordial germ cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(729974, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0101302', 'abnormal subcortical cytoplasm', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(729975, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0101577', 'abnormal notochordal epithelium', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(729976, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0141497', 'abnormal lymphoblast', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(729977, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100059', 'abnormal regenerating tail', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(729978, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0101587', 'abnormal hemangioblast', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(729979, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100267', 'abnormal wound epidermis', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(729980, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100003', 'abnormal organism subdivision', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(729981, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100701', 'abnormal microglial cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(729982, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100860', 'abnormal parathyroid', 0.5833333333333334, 12.404694921567193, 2.689994802519303, 'HP:0000828', 'Abnormality of the parathyroid gland'),
(729983, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100843', 'abnormal fasciculated network of fibrils', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(729984, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100503', 'abnormal blastomere D2', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(729985, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0107278', 'abnormal medial region', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(729986, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100032', 'abnormal nervous system', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(729987, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0115566', 'abnormal variability of size of forelimb', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(729988, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0141782', 'abnormal methylation', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(729989, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100956', 'abnormal centrosome', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(729990, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100915', 'abnormal dermal system', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(729991, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100894', 'abnormal nucleus', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(729992, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100031', 'abnormal central nervous system', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(729993, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0101857', 'abnormal endocrine system morphology', 0.43333333333333335, 6.2194654996189955, 1.6416764956901726, 'UPHENO:0003116', 'abnormal endocrine system'),
(729994, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0126542', 'abnormally localised endocrine cell', 0.40625, 6.2194654996189955, 1.5895464319170476, 'UPHENO:0003116', 'abnormal endocrine system'),
(729995, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0101157', 'abnormal female organism', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(729996, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0101347', 'abnormal hindlimb region', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(729997, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100840', 'abnormal thyroid', 0.5, 6.2194654996189955, 1.763443435386998, 'UPHENO:0003116', 'abnormal endocrine system'),
(729998, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0125007', 'absent anatomical line', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(729999, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0131745', 'abnormal axis elongation', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(730000, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0101513', 'abnormal basal body', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(730001, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100935', 'abnormal skeleton', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(730002, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100239', 'abnormal acellular anatomical structure', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(730003, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0101141', 'abnormal Keller explant', 0.5294117647058824, 1.706362323152461, 0.9504568842024205, 'UPHENO:0002536', 'abnormal anatomical entity'),
(730004, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0101090', 'abnormal adrenal gland', 0.48148148148148145, 6.2194654996189955, 1.7304789691815143, 'UPHENO:0003116', 'abnormal endocrine system'),
(730005, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0101096', 'abnormal tendon', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(730006, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0141745', 'abnormal creatinine homeostasis', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(730007, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0101212', 'abnormal glomeral mesenchyme', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(730008, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100282', 'abnormal pelvic girdle primordium', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(730009, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0141271', 'increased surface breathing', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(730010, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0131723', 'abnormal pathway-restricted SMAD protein phosphorylation', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(730011, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0126814', 'abnormally localised endocrine system', 0.4482758620689655, 6.2194654996189955, 1.669741374719419, 'UPHENO:0003116', 'abnormal endocrine system'),
(730012, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100762', 'abnormal intersomitic region', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(730013, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100799', 'abnormal genital ridge', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(730014, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0101241', 'abnormal nucleate erythrocyte', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(730015, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0101107', 'abnormal erythroid cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(730016, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100232', 'abnormal lymphatic system', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(730017, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0107267', 'abnormal ventral side', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(730018, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0101589', 'abnormal blastocoel roof', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(730019, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0141778', 'abnormal biosynthetic process', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(730020, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0101297', 'abnormal barrier cell', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(730021, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100339', 'abnormal circumblastoporal collar', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(730022, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0101110', 'abnormal cell-free extract', 0.5294117647058824, 1.706362323152461, 0.9504568842024205, 'UPHENO:0002536', 'abnormal anatomical entity'),
(730023, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0101740', 'abnormal cell part morphology', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(730024, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0101109', 'abnormal egg cell-free extract', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(730025, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0101283', 'abnormal left-ventral blastomere', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(730026, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0107261', 'abnormal dorsal-ventral axis', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(730027, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0127101', 'abnormally localised portion of organism substance', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(730028, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100067', 'abnormal animal hemisphere', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(730029, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100295', 'abnormal extracellular matrix', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(730030, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0133388', 'absent insulin receptor signaling pathway', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(730031, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100289', 'abnormal chondroblast', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(730032, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100025', 'abnormal oocyte', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(730033, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0115758', 'abnormally decreased mobility of melanoblast', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(730034, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100309', 'abnormal vegetal hemisphere', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(730035, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100726', 'abnormal tail', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(730036, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100724', 'abnormal kinetochore', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(730037, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0126624', 'abnormally localised anatomical line', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(730038, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0101553', 'abnormal dental epithelium', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(730039, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0102113', 'abnormal anatomical line morphology', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(730040, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100261', 'abnormal multilaminar epithelium', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(730041, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100285', 'abnormal progenitor cell', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(730042, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0101061', 'abnormal plasma membrane', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(730043, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100540', 'abnormal left lymph heart', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(730044, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0141272', 'absent surface breathing', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(730045, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100599', 'abnormal adult immune system', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(730046, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100070', 'abnormal anatomical system', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(730047, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100416', 'abnormal ligament', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(730048, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100192', 'abnormal epithelium', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(730049, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100823', 'abnormal blood', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(730050, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100172', 'abnormal stem cell', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(730051, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0101349', 'abnormal trunk region', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(730052, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100307', 'abnormal blastomere', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(730053, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100372', 'abnormal hematological system', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(730054, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100521', 'abnormal animal blastomere', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(730055, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100691', 'abnormal keratin accumulating cell', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(730056, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0107272', 'abnormal axial region', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(730057, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100363', 'abnormal cardiovascular system', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(730058, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0141777', 'abnormal catabolic process', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(730059, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0101099', 'abnormal ventro-lateral marginal zone', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(730060, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0107273', 'abnormal basal region', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(730061, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100616', 'abnormal ventral blood island', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(730062, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100974', 'abnormal cardiac mesoderm', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(730063, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0101004', 'abnormal acid secreting cell', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(730064, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100493', 'abnormal liver and biliary system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(730065, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100796', 'abnormal pseudoblastema', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(730066, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0101490', 'abnormal ectodermal cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(730067, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100991', 'abnormal iliac process primordium', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(730068, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0101497', 'abnormal ciliary axoneme', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(730069, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100093', 'abnormal simple squamous epithelium', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(730070, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100549', 'abnormal mitotic cell', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(730071, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100642', 'abnormal gustatory system', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(730072, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0115512', 'abnormally semi-erect whole organism', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(730073, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0101072', 'abnormal mitochondrial cloud', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(730074, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0101078', 'abnormal mucous gland', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(730075, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100531', 'abnormal proliferative region', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(730076, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0101098', 'abnormal mineralized extracellular matrix', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(730077, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0101240', 'abnormal ciliated non-epidermal cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(730078, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100667', 'abnormal vegetal yolk mass', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(730079, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0141276', 'decreased surface breathing', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(730080, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100509', 'abnormal germ plasm', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(730081, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0101570', 'abnormal forelimb region', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(730082, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100100', 'abnormal muscle', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(730083, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0101519', 'abnormal hypobranchial placode', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(730084, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0141628', 'metaplastic thymus', 0.40625, 6.2194654996189955, 1.5895464319170476, 'UPHENO:0003116', 'abnormal endocrine system'),
(730085, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100588', 'abnormal unicellular gland', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(730086, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0101237', 'abnormal mucus secreting cell', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(730087, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0141841', 'abnormality of whole organism mass', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(730088, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0141907', 'abnormal putrescine metabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(730089, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100612', 'abnormal unilaminar epithelium', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(730090, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0107312', 'abnormal filopodium', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(730091, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0141784', 'abnormal cellular hormone metabolic process', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(730092, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100858', 'abnormal presumptive midbrain-hindbrain boundary', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(730093, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100916', 'abnormal principal cavity', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(730094, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0101220', 'abnormal centriole', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(730095, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0116494', 'absent biological process', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(730096, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100249', 'abnormal avascular GAG-rich matrix', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(730097, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0107260', 'abnormal anterior-posterior axis', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(730098, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100258', 'abnormal organ part', 0.5294117647058824, 1.706362323152461, 0.9504568842024205, 'UPHENO:0002536', 'abnormal anatomical entity'),
(730099, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100902', 'abnormal spermatocyte', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(730100, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0101202', 'abnormal thymus', 0.4482758620689655, 6.2194654996189955, 1.669741374719419, 'UPHENO:0003116', 'abnormal endocrine system'),
(730101, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100816', 'abnormal blastocoel anlage', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(730102, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0101405', 'abnormal ring structure', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(730103, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0107265', 'abnormal posterior side', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(730104, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100186', 'abnormal uveal tract', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(730105, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0101132', 'abnormal apoptotic cell', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(730106, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100218', 'abnormal epithelial cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(730107, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100188', 'abnormal delta cell', 0.41935483870967744, 6.2194654996189955, 1.6149807898093176, 'UPHENO:0003116', 'abnormal endocrine system'),
(730108, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0141499', 'abnormal tadpole', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(730109, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0126321', 'abnormally localised anatomical structure', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(730110, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100551', 'abnormal oocyte cortex', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(730111, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0107288', 'abnormal larval alimentary system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(730112, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0141718', 'abnormal posterior notochord', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(730113, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0101092', 'abnormal dorso-lateral marginal zone', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(730114, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0116434', 'abnormal biological process', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(730115, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0141796', 'abnormal demethylation', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(730116, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0107266', 'abnormal dorsal side', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(730117, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100023', 'abnormal mesenchyme', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(730118, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100207', 'abnormal blastema', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(730119, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100225', 'abnormal endocrine system', 0.65, 6.2194654996189955, 2.010634868580655, 'UPHENO:0003116', 'abnormal endocrine system'),
(730120, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100004', 'abnormal cell', 0.55, 1.8210412618256888, 1.0007860380741376, 'HP:0000118', 'Phenotypic abnormality'),
(730121, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100756', 'abnormal adrenal medulla', 0.43333333333333335, 6.2194654996189955, 1.6416764956901726, 'UPHENO:0003116', 'abnormal endocrine system'),
(730122, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0141267', 'abnormal resting posture', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(730123, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0107263', 'abnormal anatomical side', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(730124, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100745', 'abnormal anterior lymph sac', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(730125, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100807', 'abnormal matrix-based tissue', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(730126, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0141775', 'abnormal nitrogen compound metabolic process', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(730127, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0131725', 'abnormal phosphorylation of RNA polymerase II C-terminal domain', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(730128, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0101498', 'abnormal stage II oocyte', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(730129, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100242', 'abnormal right lymph heart', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(730130, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100547', 'abnormal blastomere V2', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(730131, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100293', 'abnormal duct', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(730132, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100392', 'abnormal cilium', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(730133, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0131675', 'abnormal spindle microtubule', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(730134, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100108', 'abnormal cell part', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(730135, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0141809', 'abnormal catalytic activity', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(730136, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100433', 'abnormal pectoral appendage', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(730137, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100104', 'abnormal embryonic structure', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(730138, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0142052', 'abnormal nasal region', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(730139, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100727', 'abnormal odontogenic papilla', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(730140, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100437', 'abnormal proepicardium', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(730141, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100228', 'abnormal skeletal subdivision', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(730142, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100060', 'abnormal regenerating tissue', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(730143, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100255', 'abnormal pelvic appendage', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(730144, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0101713', 'abnormal anatomical entity in vitro morphology', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(730145, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100553', 'abnormal laryngeal muscle primordium', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(730146, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100268', 'abnormal circulatory system', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(730147, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0141790', 'abnormal cellular metabolic process', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(730148, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0115508', 'abnormally peramorphic growth of whole organism', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(730149, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0101575', 'abnormal vitelline membrane', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(730150, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0101269', 'abnormal mesodermal cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(730151, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100501', 'abnormal urogenital system', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(730152, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0101503', 'abnormal organ cortex', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(730153, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0141794', 'abnormal prosthetic group metabolic process', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(730154, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0101071', 'abnormal endoplasmic reticulum', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(730155, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100704', 'abnormal Merkel cell', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(730156, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0107339', 'abnormal yolk platelet', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(730157, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100734', 'abnormal lateral line system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(730158, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0101411', 'abnormal marginal zone (sensu neural)', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(730159, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100985', 'abnormal simple columnar epithelium', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(730160, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0101501', 'abnormal parabrachial area', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(730161, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0101029', 'abnormal right spleen primordium', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(730162, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0142056', 'abnormal main body axis', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(730163, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0141792', 'abnormal small molecule metabolic process', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(730164, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100317', 'abnormal respiratory system', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(730165, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0101326', 'abnormal cementoblast', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(730166, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0101187', 'abnormal dorsolateral commissural neuron', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(730167, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100002', 'abnormal head', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(730168, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100084', 'abnormal anatomical group', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(730169, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100482', 'abnormal Mullerian duct', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(730170, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0141786', 'abnormal pigment metabolic process', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(730171, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0131469', 'abnormal heart process', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(730172, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100465', 'abnormal skeletal system', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(730173, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100422', 'abnormal notochord', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(730174, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100741', 'abnormal blastopore', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(730175, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0101311', 'abnormal bottle cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(730176, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100899', 'abnormal secondary spermatogonium', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(730177, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100114', 'abnormal peripheral nervous system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(730178, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0101264', 'abnormal mitotic spindle', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(730179, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0101468', 'abnormal stage I oocyte', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(730180, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100468', 'abnormal muscular system', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(730181, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100852', 'abnormal interdigital region', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(730182, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100265', 'abnormal sensory epithelial cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(730183, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0142057', 'abnormal desmosome', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(730184, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100888', 'abnormal microtubule', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(730185, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100574', 'abnormal gastrula cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(730186, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0101378', 'abnormal blastomere D1', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(730187, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0101366', 'abnormal morula cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(730188, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0142051', 'abnormal cerebrospinal fluid', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(730189, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100256', 'abnormal paired appendage', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(730190, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100854', 'abnormal spiracle', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(730191, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100156', 'abnormal foregut', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(730192, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100081', 'abnormal anatomical entity in vitro', 0.5625, 1.706362323152461, 0.9797085315405084, 'UPHENO:0002536', 'abnormal anatomical entity'),
(730193, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0115509', 'abnormally semi-viable whole organism', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(730194, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100120', 'abnormal genital system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(730195, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0107311', 'abnormal apical junction complex', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(730196, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0107259', 'abnormal animal-vegetal axis', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(730197, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100715', 'abnormal ciliated cell', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(730198, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0141771', 'abnormal urea homeostasis', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(730199, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100010', 'abnormal multicellular anatomical structure', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(730200, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100912', 'abnormal trabecula', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(730201, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0141770', 'abnormal urate homeostasis', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(730202, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0101435', 'abnormal paracrine cell', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(730203, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0101377', 'abnormal manicotto glandulare', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(730204, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100664', 'abnormal periocular region', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(730205, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0101023', 'abnormal ultimobranchial body', 0.5652173913043478, 6.2194654996189955, 1.874926682567092, 'UPHENO:0003116', 'abnormal endocrine system'),
(730206, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0141738', 'abnormal carbon dioxide homeostasis', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(730207, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0107262', 'abnormal left-right axis', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(730208, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100152', 'abnormal alimentary system', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(730209, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0101403', 'abnormal basal lamina', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(730210, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0141781', 'abnormal secondary metabolic process', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(730211, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100146', 'abnormal primary germ layer', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(730212, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100231', 'abnormal compound organ', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(730213, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100754', 'abnormal electrically active cell', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(730214, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100176', 'abnormal stage VI oocyte', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(730215, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100201', 'abnormal cavitated compound organ', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(730216, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0101409', 'abnormal perivitelline space', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(730217, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0131685', 'abnormal cortical actin cytoskeleton', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(730218, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100786', 'abnormal presumptive axial mesoderm', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(730219, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100913', 'abnormal Brachets cleft', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(730220, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100069', 'abnormal urinary system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(730221, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100383', 'abnormal amputated fin', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(730222, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100605', 'abnormal prechordal plate', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(730223, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100202', 'abnormal embryo', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(730224, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100735', 'abnormal hindgut', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(730225, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100707', 'abnormal central vegetal yolk mass', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(730226, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100791', 'abnormal multiciliated cell precursor', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(730227, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100164', 'abnormal neural nucleus', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(730228, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0141600', 'absent metamorphosis', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(730229, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0141629', 'metaplastic thyroid', 0.4482758620689655, 6.2194654996189955, 1.669741374719419, 'UPHENO:0003116', 'abnormal endocrine system'),
(730230, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0131677', 'abnormal actin filament', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(730231, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100196', 'abnormal neuron', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(730232, 'HP:0000828', 'Abnormality of the parathyroid gland', 'XPO:0100742', 'abnormal musculoskeletal system', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(730233, 'HP:0002038', 'Protein avoidance', 'XPO:0141717', 'abnormal tracheoesophageal fold', 0.42857142857142855, 5.05060299610679, 1.471238981671103, 'HP:0025031', 'Abnormality of the digestive system'),
(730234, 'HP:0002038', 'Protein avoidance', 'XPO:0107305', 'abnormal dorsal posterior hindgut endoderm', 0.4166666666666667, 5.05060299610679, 1.45066119926208, 'HP:0025031', 'Abnormality of the digestive system'),
(730235, 'HP:0002038', 'Protein avoidance', 'XPO:0107288', 'abnormal larval alimentary system', 0.5172413793103449, 5.05060299610679, 1.6162861318637973, 'HP:0025031', 'Abnormality of the digestive system'),
(730236, 'HP:0002038', 'Protein avoidance', 'XPO:0142054', 'abnormal digestive tract', 0.5, 5.05060299610679, 1.5891197242666757, 'HP:0025031', 'Abnormality of the digestive system'),
(730237, 'HP:0002038', 'Protein avoidance', 'XPO:0141833', 'edematous alimentary system', 0.41025641025641024, 5.05060299610679, 1.4394590146346793, 'HP:0025031', 'Abnormality of the digestive system'),
(730238, 'HP:0002038', 'Protein avoidance', 'XPO:0107375', 'abnormal larval alimentary system morphology', 0.41025641025641024, 5.05060299610679, 1.4394590146346793, 'HP:0025031', 'Abnormality of the digestive system'),
(730239, 'HP:0002038', 'Protein avoidance', 'XPO:0142061', 'abnormal digestive tract morphology', 0.41025641025641024, 5.05060299610679, 1.4394590146346793, 'HP:0025031', 'Abnormality of the digestive system'),
(730240, 'HP:0002038', 'Protein avoidance', 'XPO:0100214', 'abnormal second pancreatic bud', 0.42857142857142855, 5.05060299610679, 1.471238981671103, 'HP:0025031', 'Abnormality of the digestive system'),
(730241, 'HP:0002038', 'Protein avoidance', 'XPO:0127721', 'abnormally localised manicotto glandulare', 0.41025641025641024, 5.05060299610679, 1.4394590146346793, 'HP:0025031', 'Abnormality of the digestive system'),
(730242, 'HP:0002038', 'Protein avoidance', 'XPO:0126608', 'abnormally localised foregut', 0.42105263157894735, 5.05060299610679, 1.4582762710032966, 'HP:0025031', 'Abnormality of the digestive system'),
(730243, 'HP:0002038', 'Protein avoidance', 'XPO:0124857', 'absent alimentary system', 0.43243243243243246, 5.05060299610679, 1.4778513250178418, 'HP:0025031', 'Abnormality of the digestive system'),
(730244, 'HP:0002038', 'Protein avoidance', 'XPO:0100462', 'abnormal anterior foregut', 0.46875, 5.05060299610679, 1.5386585568036393, 'HP:0025031', 'Abnormality of the digestive system'),
(730245, 'HP:0002038', 'Protein avoidance', 'XPO:0127307', 'abnormally localised oral evagination', 0.42105263157894735, 5.05060299610679, 1.4582762710032966, 'HP:0025031', 'Abnormality of the digestive system'),
(730246, 'HP:0002038', 'Protein avoidance', 'XPO:0100486', 'abnormal oral evagination', 0.4838709677419355, 5.05060299610679, 1.5632786569919361, 'HP:0025031', 'Abnormality of the digestive system'),
(730247, 'HP:0002038', 'Protein avoidance', 'XPO:0127838', 'abnormally localised dorsal foregut', 0.41025641025641024, 5.05060299610679, 1.4394590146346793, 'HP:0025031', 'Abnormality of the digestive system'),
(730248, 'HP:0002038', 'Protein avoidance', 'XPO:0101021', 'abnormal dorsal foregut', 0.46875, 5.05060299610679, 1.5386585568036393, 'HP:0025031', 'Abnormality of the digestive system'),
(730249, 'HP:0002038', 'Protein avoidance', 'XPO:0100188', 'abnormal delta cell', 0.40540540540540543, 5.05060299610679, 1.4309233924911664, 'HP:0025031', 'Abnormality of the digestive system'),
(730250, 'HP:0002038', 'Protein avoidance', 'XPO:0100216', 'abnormal hepato-pancreatic progenitor cell', 0.4166666666666667, 5.05060299610679, 1.45066119926208, 'HP:0025031', 'Abnormality of the digestive system'),
(730251, 'HP:0002038', 'Protein avoidance', 'XPO:0125663', 'absent oral evagination', 0.41025641025641024, 5.05060299610679, 1.4394590146346793, 'HP:0025031', 'Abnormality of the digestive system'),
(730252, 'HP:0002038', 'Protein avoidance', 'XPO:0126499', 'abnormally localised liver and biliary system', 0.43243243243243246, 5.05060299610679, 1.4778513250178418, 'HP:0025031', 'Abnormality of the digestive system'),
(730253, 'HP:0002038', 'Protein avoidance', 'XPO:0107304', 'abnormal hindgut endoderm', 0.4411764705882353, 5.05060299610679, 1.4927180591674907, 'HP:0025031', 'Abnormality of the digestive system'),
(730254, 'HP:0002038', 'Protein avoidance', 'XPO:0100735', 'abnormal hindgut', 0.4838709677419355, 5.05060299610679, 1.5632786569919361, 'HP:0025031', 'Abnormality of the digestive system'),
(730255, 'HP:0002038', 'Protein avoidance', 'XPO:0100152', 'abnormal alimentary system', 0.5357142857142857, 5.05060299610679, 1.6448951870820767, 'HP:0025031', 'Abnormality of the digestive system'),
(730256, 'HP:0002038', 'Protein avoidance', 'XPO:0125084', 'absent larval alimentary system', 0.41025641025641024, 5.05060299610679, 1.4394590146346793, 'HP:0025031', 'Abnormality of the digestive system'),
(730257, 'HP:0002038', 'Protein avoidance', 'XPO:0101377', 'abnormal manicotto glandulare', 0.4838709677419355, 5.05060299610679, 1.5632786569919361, 'HP:0025031', 'Abnormality of the digestive system'),
(730258, 'HP:0002038', 'Protein avoidance', 'XPO:0100718', 'abnormal ventral pancreatic bud', 0.45454545454545453, 5.05060299610679, 1.5151662069205463, 'HP:0025031', 'Abnormality of the digestive system'),
(730259, 'HP:0002038', 'Protein avoidance', 'XPO:0124888', 'absent liver and biliary system', 0.42105263157894735, 5.05060299610679, 1.4582762710032966, 'HP:0025031', 'Abnormality of the digestive system'),
(730260, 'HP:0002038', 'Protein avoidance', 'XPO:0100454', 'abnormal lung bud', 0.40540540540540543, 5.05060299610679, 1.4309233924911664, 'HP:0025031', 'Abnormality of the digestive system'),
(730261, 'HP:0002038', 'Protein avoidance', 'XPO:0126705', 'abnormally localised larval alimentary system', 0.42105263157894735, 5.05060299610679, 1.4582762710032966, 'HP:0025031', 'Abnormality of the digestive system'),
(730262, 'HP:0002038', 'Protein avoidance', 'XPO:0131662', 'abnormal foregut epithelium', 0.4166666666666667, 5.05060299610679, 1.45066119926208, 'HP:0025031', 'Abnormality of the digestive system'),
(730263, 'HP:0002038', 'Protein avoidance', 'XPO:0102125', 'abnormal liver and biliary system morphology', 0.41025641025641024, 5.05060299610679, 1.4394590146346793, 'HP:0025031', 'Abnormality of the digestive system'),
(730264, 'HP:0002038', 'Protein avoidance', 'XPO:0101381', 'abnormal ventral foregut', 0.46875, 5.05060299610679, 1.5386585568036393, 'HP:0025031', 'Abnormality of the digestive system'),
(730265, 'HP:0002038', 'Protein avoidance', 'XPO:0115495', 'abnormally protruding proctodeum', 0.45714285714285713, 5.05060299610679, 1.519489086480891, 'HP:0025031', 'Abnormality of the digestive system'),
(730266, 'HP:0002038', 'Protein avoidance', 'XPO:0100493', 'abnormal liver and biliary system', 0.5172413793103449, 5.05060299610679, 1.6162861318637973, 'HP:0025031', 'Abnormality of the digestive system'),
(730267, 'HP:0002038', 'Protein avoidance', 'XPO:0125745', 'absent pharyngeal cavity', 0.43243243243243246, 5.05060299610679, 1.4778513250178418, 'HP:0025031', 'Abnormality of the digestive system'),
(730268, 'HP:0002038', 'Protein avoidance', 'XPO:0107308', 'abnormal anterior hindgut endoderm', 0.42857142857142855, 5.05060299610679, 1.471238981671103, 'HP:0025031', 'Abnormality of the digestive system'),
(730269, 'HP:0002038', 'Protein avoidance', 'XPO:0142020', 'absent digestive tract', 0.41025641025641024, 5.05060299610679, 1.4394590146346793, 'HP:0025031', 'Abnormality of the digestive system'),
(730270, 'HP:0002038', 'Protein avoidance', 'XPO:0101601', 'abnormal proctodeum', 0.45454545454545453, 5.05060299610679, 1.5151662069205463, 'HP:0025031', 'Abnormality of the digestive system'),
(730271, 'HP:0002038', 'Protein avoidance', 'XPO:0126466', 'abnormally localised alimentary system', 0.4444444444444444, 5.05060299610679, 1.4982364441950171, 'HP:0025031', 'Abnormality of the digestive system'),
(730272, 'HP:0002038', 'Protein avoidance', 'XPO:0100215', 'abnormal first pancreatic bud', 0.4411764705882353, 5.05060299610679, 1.4927180591674907, 'HP:0025031', 'Abnormality of the digestive system'),
(730273, 'HP:0002038', 'Protein avoidance', 'XPO:0115391', 'abnormally undifferentiated alimentary system', 0.5172413793103449, 5.05060299610679, 1.6162861318637973, 'HP:0025031', 'Abnormality of the digestive system'),
(730274, 'HP:0002038', 'Protein avoidance', 'XPO:0100156', 'abnormal foregut', 0.4838709677419355, 5.05060299610679, 1.5632786569919361, 'HP:0025031', 'Abnormality of the digestive system'),
(730275, 'HP:0002038', 'Protein avoidance', 'XPO:0100494', 'abnormal liver diverticulum', 0.40540540540540543, 5.05060299610679, 1.4309233924911664, 'HP:0025031', 'Abnormality of the digestive system'),
(730276, 'HP:0002038', 'Protein avoidance', 'XPO:0101169', 'abnormal hepato-pancreatic duct', 0.45454545454545453, 5.05060299610679, 1.5151662069205463, 'HP:0025031', 'Abnormality of the digestive system'),
(730277, 'HP:0002038', 'Protein avoidance', 'XPO:0127393', 'abnormally localised pharyngeal cavity', 0.4444444444444444, 5.05060299610679, 1.4982364441950171, 'HP:0025031', 'Abnormality of the digestive system'),
(730278, 'HP:0002038', 'Protein avoidance', 'XPO:0107307', 'abnormal posterior hindgut endoderm', 0.42857142857142855, 5.05060299610679, 1.471238981671103, 'HP:0025031', 'Abnormality of the digestive system'),
(730279, 'HP:0002038', 'Protein avoidance', 'XPO:0100893', 'abnormal hyoid arch', 0.40540540540540543, 5.05060299610679, 1.4309233924911664, 'HP:0025031', 'Abnormality of the digestive system'),
(730280, 'HP:0002038', 'Protein avoidance', 'XPO:0100591', 'abnormal pharyngeal arch', 0.4166666666666667, 5.05060299610679, 1.45066119926208, 'HP:0025031', 'Abnormality of the digestive system'),
(730281, 'HP:0002038', 'Protein avoidance', 'XPO:0100523', 'abnormal midgut', 0.4838709677419355, 5.05060299610679, 1.5632786569919361, 'HP:0025031', 'Abnormality of the digestive system'),
(730282, 'HP:0002038', 'Protein avoidance', 'XPO:0127678', 'abnormally localised ventral foregut', 0.41025641025641024, 5.05060299610679, 1.4394590146346793, 'HP:0025031', 'Abnormality of the digestive system'),
(730283, 'HP:0002038', 'Protein avoidance', 'XPO:0131673', 'abnormal buccopharyngeal membrane', 0.40540540540540543, 5.05060299610679, 1.4309233924911664, 'HP:0025031', 'Abnormality of the digestive system'),
(730284, 'HP:0002038', 'Protein avoidance', 'XPO:0131683', 'abnormal stomach epithelium', 0.4166666666666667, 5.05060299610679, 1.45066119926208, 'HP:0025031', 'Abnormality of the digestive system'),
(730285, 'HP:0002038', 'Protein avoidance', 'XPO:0100890', 'abnormal pharyngeal cavity', 0.5, 5.05060299610679, 1.5891197242666757, 'HP:0025031', 'Abnormality of the digestive system'),
(730286, 'HP:0002038', 'Protein avoidance', 'XPO:0101784', 'abnormal alimentary system morphology', 0.43243243243243246, 5.05060299610679, 1.4778513250178418, 'HP:0025031', 'Abnormality of the digestive system'),
(730287, 'HP:0002038', 'Protein avoidance', 'XPO:0101103', 'abnormal pharyngeal mesenchyme', 0.40540540540540543, 5.05060299610679, 1.4309233924911664, 'HP:0025031', 'Abnormality of the digestive system'),
(730288, 'HP:0002038', 'Protein avoidance', 'XPO:0101198', 'abnormal digestive enzyme secreting cell', 0.4411764705882353, 5.05060299610679, 1.4927180591674907, 'HP:0025031', 'Abnormality of the digestive system'),
(730289, 'HP:0002038', 'Protein avoidance', 'XPO:0100986', 'abnormal gut epithelium', 0.46875, 5.05060299610679, 1.5386585568036393, 'HP:0025031', 'Abnormality of the digestive system'),
(730290, 'HP:0002038', 'Protein avoidance', 'XPO:0100130', 'abnormal mouth primordium', 0.4166666666666667, 5.05060299610679, 1.45066119926208, 'HP:0025031', 'Abnormality of the digestive system'),
(730291, 'HP:0002038', 'Protein avoidance', 'XPO:0115392', 'abnormally incomplete structure of alimentary system', 0.42105263157894735, 5.05060299610679, 1.4582762710032966, 'HP:0025031', 'Abnormality of the digestive system'),
(730292, 'HP:0002038', 'Protein avoidance', 'XPO:0126837', 'abnormally localised midgut', 0.42105263157894735, 5.05060299610679, 1.4582762710032966, 'HP:0025031', 'Abnormality of the digestive system'),
(730293, 'HP:0002038', 'Protein avoidance', 'XPO:0126520', 'abnormally localised hindgut', 0.42105263157894735, 5.05060299610679, 1.4582762710032966, 'HP:0025031', 'Abnormality of the digestive system'),
(730294, 'HP:0002038', 'Protein avoidance', 'XPO:0101101', 'abnormal posterior foregut', 0.46875, 5.05060299610679, 1.5386585568036393, 'HP:0025031', 'Abnormality of the digestive system'),
(730295, 'HP:0002038', 'Protein avoidance', 'XPO:0127173', 'abnormally localised anterior foregut', 0.41025641025641024, 5.05060299610679, 1.4394590146346793, 'HP:0025031', 'Abnormality of the digestive system'),
(730296, 'HP:0002038', 'Protein avoidance', 'XPO:0142027', 'abnormally localised digestive tract', 0.42105263157894735, 5.05060299610679, 1.4582762710032966, 'HP:0025031', 'Abnormality of the digestive system'),
(730297, 'HP:0002038', 'Protein avoidance', 'XPO:0107306', 'abnormal ventral posterior hindgut endoderm', 0.4166666666666667, 5.05060299610679, 1.45066119926208, 'HP:0025031', 'Abnormality of the digestive system'),
(730298, 'HP:0002038', 'Protein avoidance', 'XPO:0102522', 'abnormal pharyngeal cavity morphology', 0.43243243243243246, 5.05060299610679, 1.4778513250178418, 'HP:0025031', 'Abnormality of the digestive system'),
(730299, 'HP:0002038', 'Protein avoidance', 'XPO:0101084', 'abnormal mesentery', 0.40540540540540543, 5.05060299610679, 1.4309233924911664, 'HP:0025031', 'Abnormality of the digestive system'),
(730300, 'HP:0002038', 'Protein avoidance', 'XPO:0100492', 'abnormal gall bladder primordium', 0.4411764705882353, 5.05060299610679, 1.4927180591674907, 'HP:0025031', 'Abnormality of the digestive system'),
(730301, 'HP:0002038', 'Protein avoidance', 'XPO:0100621', 'abnormal peritoneum', 0.4411764705882353, 5.05060299610679, 1.4927180591674907, 'HP:0025031', 'Abnormality of the digestive system'),
(730302, 'HP:0002038', 'Protein avoidance', 'XPO:0126425', 'abnormally localised posterior foregut', 0.41025641025641024, 5.05060299610679, 1.4394590146346793, 'HP:0025031', 'Abnormality of the digestive system'),
(730303, 'HP:0002038', 'Protein avoidance', 'XPO:0100572', 'abnormal branchial arch', 0.40540540540540543, 5.05060299610679, 1.4309233924911664, 'HP:0025031', 'Abnormality of the digestive system'),
(730304, 'HP:0007950', 'Peripapillary chorioretinal atrophy', 'XPO:0102805', 'abnormal retinal layer morphology', 0.4942528735632184, 8.040873045973026, 1.9935457378573478, 'HP:0000479', 'Abnormal retinal morphology'),
(730305, 'HP:0007950', 'Peripapillary chorioretinal atrophy', 'XPO:0103184', 'abnormal inner limiting membrane morphology', 0.4174757281553398, 8.040873045973026, 1.8321761186829812, 'HP:0000479', 'Abnormal retinal morphology'),
(730306, 'HP:0007950', 'Peripapillary chorioretinal atrophy', 'XPO:0141333', 'increased pigmentation in the retinal pigmented epithelium', 0.4056603773584906, 8.040873045973026, 1.8060630094548564, 'HP:0000479', 'Abnormal retinal morphology'),
(730307, 'HP:0007950', 'Peripapillary chorioretinal atrophy', 'XPO:0103226', 'abnormal retinal outer plexiform layer morphology', 0.4174757281553398, 8.040873045973026, 1.8321761186829812, 'HP:0000479', 'Abnormal retinal morphology'),
(730308, 'HP:0007950', 'Peripapillary chorioretinal atrophy', 'XPO:0102441', 'abnormal retinal inner plexiform layer morphology', 0.4174757281553398, 8.040873045973026, 1.8321761186829812, 'HP:0000479', 'Abnormal retinal morphology'),
(730309, 'HP:0007950', 'Peripapillary chorioretinal atrophy', 'XPO:0130257', 'increased size of the retinal blood vessel', 0.5192307692307693, 10.24626555896271, 2.306550746877889, 'UPHENO:0087915', 'abnormal vasculature of eye morphology'),
(730310, 'HP:0007950', 'Peripapillary chorioretinal atrophy', 'XPO:0140553', 'abnormally necrotic retinal stem cell region', 0.4479166666666667, 8.040873045973026, 1.8977990019604511, 'HP:0000479', 'Abnormal retinal morphology'),
(730311, 'HP:0007950', 'Peripapillary chorioretinal atrophy', 'XPO:0140192', 'abnormally necrotic retina', 0.4574468085106383, 8.040873045973026, 1.9178820903589395, 'HP:0000479', 'Abnormal retinal morphology'),
(730312, 'HP:0007950', 'Peripapillary chorioretinal atrophy', 'XPO:0130148', 'increased size of the ciliary marginal zone', 0.40186915887850466, 8.040873045973026, 1.797603651429875, 'HP:0000479', 'Abnormal retinal morphology'),
(730313, 'HP:0007950', 'Peripapillary chorioretinal atrophy', 'XPO:0102342', 'abnormal hyaloid vein morphology', 0.4375, 10.24626555896271, 2.1172484932209032, 'UPHENO:0087915', 'abnormal vasculature of eye morphology'),
(730314, 'HP:0007950', 'Peripapillary chorioretinal atrophy', 'XPO:0140489', 'abnormally necrotic ciliary marginal zone', 0.4095238095238095, 8.040873045973026, 1.8146429295275122, 'HP:0000479', 'Abnormal retinal morphology'),
(730315, 'HP:0007950', 'Peripapillary chorioretinal atrophy', 'XPO:0128475', 'decreased size of the retinal stem cell region', 0.4387755102040816, 8.040873045973026, 1.8783338822565765, 'HP:0000479', 'Abnormal retinal morphology'),
(730316, 'HP:0007950', 'Peripapillary chorioretinal atrophy', 'XPO:0102266', 'abnormal horizontal cell morphology', 0.40186915887850466, 8.040873045973026, 1.797603651429875, 'HP:0000479', 'Abnormal retinal morphology'),
(730317, 'HP:0007950', 'Peripapillary chorioretinal atrophy', 'XPO:0102232', 'abnormal eye photoreceptor cell morphology', 0.4056603773584906, 8.040873045973026, 1.8060630094548564, 'HP:0000479', 'Abnormal retinal morphology'),
(730318, 'HP:0007950', 'Peripapillary chorioretinal atrophy', 'XPO:0140487', 'abnormally necrotic retinal layer', 0.46236559139784944, 8.040873045973026, 1.9281657141584967, 'HP:0000479', 'Abnormal retinal morphology'),
(730319, 'HP:0007950', 'Peripapillary chorioretinal atrophy', 'XPO:0128669', 'decreased size of the ciliary marginal zone', 0.40186915887850466, 8.040873045973026, 1.797603651429875, 'HP:0000479', 'Abnormal retinal morphology'),
(730320, 'HP:0007950', 'Peripapillary chorioretinal atrophy', 'XPO:0140161', 'abnormally necrotic hyaloid vascular plexus', 0.40384615384615385, 10.24626555896271, 2.0341865541963946, 'UPHENO:0087915', 'abnormal vasculature of eye morphology'),
(730321, 'HP:0007950', 'Peripapillary chorioretinal atrophy', 'XPO:0100779', 'abnormal optic choroid vascular plexus', 0.4567901234567901, 9.463856994035337, 2.079181667070679, 'UPHENO:0005090', 'abnormal vasculature of eye'),
(730322, 'HP:0007950', 'Peripapillary chorioretinal atrophy', 'XPO:0102162', 'abnormal ciliary marginal zone morphology', 0.44329896907216493, 8.040873045973026, 1.8879911895239345, 'HP:0000479', 'Abnormal retinal morphology'),
(730323, 'HP:0007950', 'Peripapillary chorioretinal atrophy', 'XPO:0129780', 'increased size of the retina', 0.4479166666666667, 8.040873045973026, 1.8977990019604511, 'HP:0000479', 'Abnormal retinal morphology'),
(730324, 'HP:0007950', 'Peripapillary chorioretinal atrophy', 'XPO:0102996', 'abnormal optic fiber layer morphology', 0.4174757281553398, 8.040873045973026, 1.8321761186829812, 'HP:0000479', 'Abnormal retinal morphology'),
(730325, 'HP:0007950', 'Peripapillary chorioretinal atrophy', 'XPO:0140754', 'abnormally necrotic optic choroid vascular plexus', 0.5247524752475248, 11.854497839006713, 2.494128521916063, 'HP:0000610', 'Abnormal choroid morphology'),
(730326, 'HP:0007950', 'Peripapillary chorioretinal atrophy', 'XPO:0128787', 'decreased size of the peripheral retina', 0.43, 8.040873045973026, 1.859455675666511, 'HP:0000479', 'Abnormal retinal morphology'),
(730327, 'HP:0007950', 'Peripapillary chorioretinal atrophy', 'XPO:0129955', 'increased size of the retinal stem cell region', 0.4387755102040816, 8.040873045973026, 1.8783338822565765, 'HP:0000479', 'Abnormal retinal morphology'),
(730328, 'HP:0007950', 'Peripapillary chorioretinal atrophy', 'XPO:0128935', 'decreased size of the central retina', 0.4574468085106383, 8.040873045973026, 1.9178820903589395, 'HP:0000479', 'Abnormal retinal morphology'),
(730329, 'HP:0007950', 'Peripapillary chorioretinal atrophy', 'XPO:0125909', 'absent retinal blood vessel', 0.5051546391752577, 9.463856994035337, 2.186483767382726, 'UPHENO:0005090', 'abnormal vasculature of eye'),
(730330, 'HP:0007950', 'Peripapillary chorioretinal atrophy', 'XPO:0102196', 'abnormal central retina morphology', 0.48314606741573035, 8.040873045973026, 1.9710190741722953, 'HP:0000479', 'Abnormal retinal morphology'),
(730331, 'HP:0007950', 'Peripapillary chorioretinal atrophy', 'XPO:0101861', 'abnormal photoreceptor layer morphology', 0.4215686274509804, 8.040873045973026, 1.8411354685352277, 'HP:0000479', 'Abnormal retinal morphology'),
(730332, 'HP:0007950', 'Peripapillary chorioretinal atrophy', 'XPO:0102946', 'abnormal retinal inner nuclear layer morphology', 0.4174757281553398, 8.040873045973026, 1.8321761186829812, 'HP:0000479', 'Abnormal retinal morphology'),
(730333, 'HP:0007950', 'Peripapillary chorioretinal atrophy', 'XPO:0140317', 'abnormally necrotic retinal progenitor cell', 0.40186915887850466, 8.040873045973026, 1.797603651429875, 'HP:0000479', 'Abnormal retinal morphology'),
(730334, 'HP:0007950', 'Peripapillary chorioretinal atrophy', 'XPO:0127230', 'abnormally localised hyaloid blood vessel', 0.4157303370786517, 9.463856994035337, 1.9835353433187084, 'UPHENO:0005090', 'abnormal vasculature of eye'),
(730335, 'HP:0007950', 'Peripapillary chorioretinal atrophy', 'XPO:0101315', 'abnormal hyaloid vascular plexus', 0.45121951219512196, 9.463856994035337, 2.0664648403331274, 'UPHENO:0005090', 'abnormal vasculature of eye'),
(730336, 'HP:0007950', 'Peripapillary chorioretinal atrophy', 'XPO:0130044', 'increased size of the hyaloid blood vessel', 0.4375, 10.24626555896271, 2.1172484932209032, 'UPHENO:0087915', 'abnormal vasculature of eye morphology'),
(730337, 'HP:0007950', 'Peripapillary chorioretinal atrophy', 'XPO:0129810', 'increased size of the retinal progenitor cell region', 0.4387755102040816, 8.040873045973026, 1.8783338822565765, 'HP:0000479', 'Abnormal retinal morphology'),
(730338, 'HP:0007950', 'Peripapillary chorioretinal atrophy', 'XPO:0102505', 'abnormal retinal stem cell region morphology', 0.46236559139784944, 8.040873045973026, 1.9281657141584967, 'HP:0000479', 'Abnormal retinal morphology'),
(730339, 'HP:0007950', 'Peripapillary chorioretinal atrophy', 'XPO:0102117', 'abnormal retina morphology', 0.48314606741573035, 8.040873045973026, 1.9710190741722953, 'HP:0000479', 'Abnormal retinal morphology'),
(730340, 'HP:0007950', 'Peripapillary chorioretinal atrophy', 'XPO:0102756', 'abnormal Muller cell morphology', 0.44329896907216493, 8.040873045973026, 1.8879911895239345, 'HP:0000479', 'Abnormal retinal morphology'),
(730341, 'HP:0007950', 'Peripapillary chorioretinal atrophy', 'XPO:0103186', 'abnormal peripheral retina morphology', 0.4673913043478261, 8.040873045973026, 1.938616553383523, 'HP:0000479', 'Abnormal retinal morphology'),
(730342, 'HP:0007950', 'Peripapillary chorioretinal atrophy', 'XPO:0140531', 'abnormally necrotic retinal progenitor cell region', 0.4479166666666667, 8.040873045973026, 1.8977990019604511, 'HP:0000479', 'Abnormal retinal morphology'),
(730343, 'HP:0007950', 'Peripapillary chorioretinal atrophy', 'XPO:0139887', 'abnormally necrotic Muller cell', 0.4215686274509804, 8.040873045973026, 1.8411354685352277, 'HP:0000479', 'Abnormal retinal morphology'),
(730344, 'HP:0007950', 'Peripapillary chorioretinal atrophy', 'XPO:0127563', 'abnormally localised retinal blood vessel', 0.532608695652174, 9.463856994035337, 2.245113032662691, 'HP:0008047', 'Abnormality of the vasculature of the eye'),
(730345, 'HP:0007950', 'Peripapillary chorioretinal atrophy', 'XPO:0125589', 'absent hyaloid blood vessel', 0.40217391304347827, 9.463856994035337, 1.9509270616235455, 'UPHENO:0005090', 'abnormal vasculature of eye'),
(730346, 'HP:0007950', 'Peripapillary chorioretinal atrophy', 'XPO:0130122', 'increased size of the retinal layer', 0.4574468085106383, 8.040873045973026, 1.9178820903589395, 'HP:0000479', 'Abnormal retinal morphology'),
(730347, 'HP:0007950', 'Peripapillary chorioretinal atrophy', 'XPO:0102818', 'abnormal optic chiasm morphology', 0.4019607843137255, 7.796308075334707, 1.7702570741880883, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(730348, 'HP:0007950', 'Peripapillary chorioretinal atrophy', 'XPO:0100329', 'abnormal retinal blood vessel', 0.5975609756097561, 9.463856994035337, 2.378073089370251, 'UPHENO:0005090', 'abnormal vasculature of eye'),
(730349, 'HP:0007950', 'Peripapillary chorioretinal atrophy', 'XPO:0102939', 'abnormal retinal ganglion cell layer morphology', 0.4174757281553398, 8.040873045973026, 1.8321761186829812, 'HP:0000479', 'Abnormal retinal morphology'),
(730350, 'HP:0007950', 'Peripapillary chorioretinal atrophy', 'XPO:0102450', 'abnormal retinal stem cell morphology', 0.4215686274509804, 8.040873045973026, 1.8411354685352277, 'HP:0000479', 'Abnormal retinal morphology'),
(730351, 'HP:0007950', 'Peripapillary chorioretinal atrophy', 'XPO:0100371', 'abnormal hyaloid blood vessel', 0.4625, 9.463856994035337, 2.0921361953136186, 'HP:0008047', 'Abnormality of the vasculature of the eye'),
(730352, 'HP:0007950', 'Peripapillary chorioretinal atrophy', 'XPO:0101961', 'abnormal retinal blood vessel morphology', 0.5684210526315789, 10.24626555896271, 2.4133364984121624, 'UPHENO:0087915', 'abnormal vasculature of eye morphology'),
(730353, 'HP:0007950', 'Peripapillary chorioretinal atrophy', 'XPO:0128779', 'decreased size of the retinal blood vessel', 0.5192307692307693, 10.24626555896271, 2.306550746877889, 'UPHENO:0087915', 'abnormal vasculature of eye morphology'),
(730354, 'HP:0007950', 'Peripapillary chorioretinal atrophy', 'XPO:0128643', 'decreased size of the retinal layer', 0.4574468085106383, 8.040873045973026, 1.9178820903589395, 'HP:0000479', 'Abnormal retinal morphology'),
(730355, 'HP:0007950', 'Peripapillary chorioretinal atrophy', 'XPO:0128300', 'decreased size of the retina', 0.4479166666666667, 8.040873045973026, 1.8977990019604511, 'HP:0000479', 'Abnormal retinal morphology'),
(730356, 'HP:0007950', 'Peripapillary chorioretinal atrophy', 'XPO:0128564', 'decreased size of the hyaloid blood vessel', 0.4375, 10.24626555896271, 2.1172484932209032, 'UPHENO:0087915', 'abnormal vasculature of eye morphology'),
(730357, 'HP:0007950', 'Peripapillary chorioretinal atrophy', 'XPO:0140346', 'abnormally necrotic retinal blood vessel', 0.5294117647058824, 10.24626555896271, 2.3290542138850165, 'UPHENO:0087915', 'abnormal vasculature of eye morphology'),
(730358, 'HP:0007950', 'Peripapillary chorioretinal atrophy', 'XPO:0128330', 'decreased size of the retinal progenitor cell region', 0.4387755102040816, 8.040873045973026, 1.8783338822565765, 'HP:0000479', 'Abnormal retinal morphology'),
(730359, 'HP:0007950', 'Peripapillary chorioretinal atrophy', 'XPO:0102991', 'abnormal hyaloid artery morphology', 0.42990654205607476, 10.24626555896271, 2.0987940812385366, 'UPHENO:0087915', 'abnormal vasculature of eye morphology'),
(730360, 'HP:0007950', 'Peripapillary chorioretinal atrophy', 'XPO:0139722', 'abnormally necrotic hyaloid blood vessel', 0.44680851063829785, 10.24626555896271, 2.1396538631294115, 'UPHENO:0087915', 'abnormal vasculature of eye morphology'),
(730361, 'HP:0007950', 'Peripapillary chorioretinal atrophy', 'XPO:0130013', 'increased size of the optic choroid vascular plexus', 0.5145631067961165, 11.854497839006713, 2.469794978848881, 'HP:0000610', 'Abnormal choroid morphology'),
(730362, 'HP:0007950', 'Peripapillary chorioretinal atrophy', 'XPO:0102947', 'abnormal hyaloid vascular plexus morphology', 0.4421052631578947, 10.24626555896271, 2.128362734904669, 'UPHENO:0087915', 'abnormal vasculature of eye morphology'),
(730363, 'HP:0007950', 'Peripapillary chorioretinal atrophy', 'XPO:0140439', 'abnormally necrotic retinal stem cell', 0.40186915887850466, 8.040873045973026, 1.797603651429875, 'HP:0000479', 'Abnormal retinal morphology'),
(730364, 'HP:0007950', 'Peripapillary chorioretinal atrophy', 'XPO:0102411', 'abnormal optic choroid vascular plexus morphology', 0.5698924731182796, 11.854497839006713, 2.5991900836696873, 'HP:0000610', 'Abnormal choroid morphology'),
(730365, 'HP:0007950', 'Peripapillary chorioretinal atrophy', 'XPO:0102963', 'abnormal retinal outer nuclear layer morphology', 0.4174757281553398, 8.040873045973026, 1.8321761186829812, 'HP:0000479', 'Abnormal retinal morphology'),
(730366, 'HP:0007950', 'Peripapillary chorioretinal atrophy', 'XPO:0102003', 'abnormal hyaloid blood vessel morphology', 0.4772727272727273, 10.24626555896271, 2.2113939286537683, 'UPHENO:0087915', 'abnormal vasculature of eye morphology'),
(730367, 'HP:0007950', 'Peripapillary chorioretinal atrophy', 'XPO:0140271', 'abnormally necrotic peripheral retina', 0.4387755102040816, 8.040873045973026, 1.8783338822565765, 'HP:0000479', 'Abnormal retinal morphology'),
(730368, 'HP:0007950', 'Peripapillary chorioretinal atrophy', 'XPO:0130413', 'increased size of the central retina', 0.4574468085106383, 8.040873045973026, 1.9178820903589395, 'HP:0000479', 'Abnormal retinal morphology'),
(730369, 'HP:0007950', 'Peripapillary chorioretinal atrophy', 'XPO:0127907', 'abnormally localised optic choroid vascular plexus', 0.40217391304347827, 9.463856994035337, 1.9509270616235455, 'UPHENO:0005090', 'abnormal vasculature of eye'),
(730370, 'HP:0007950', 'Peripapillary chorioretinal atrophy', 'XPO:0140391', 'abnormally necrotic central retina', 0.4673913043478261, 8.040873045973026, 1.938616553383523, 'HP:0000479', 'Abnormal retinal morphology'),
(730371, 'HP:0007950', 'Peripapillary chorioretinal atrophy', 'XPO:0102663', 'abnormal retinal progenitor cell morphology', 0.4215686274509804, 8.040873045973026, 1.8411354685352277, 'HP:0000479', 'Abnormal retinal morphology'),
(730372, 'HP:0007950', 'Peripapillary chorioretinal atrophy', 'XPO:0102784', 'abnormal retinal progenitor cell region morphology', 0.46236559139784944, 8.040873045973026, 1.9281657141584967, 'HP:0000479', 'Abnormal retinal morphology'),
(730373, 'HP:0007950', 'Peripapillary chorioretinal atrophy', 'XPO:0141253', 'abnormally necrotic hyaloid vein', 0.40384615384615385, 10.24626555896271, 2.0341865541963946, 'UPHENO:0087915', 'abnormal vasculature of eye morphology'),
(730374, 'HP:0007950', 'Peripapillary chorioretinal atrophy', 'XPO:0102239', 'abnormal retinal pigmented epithelium morphology', 0.4174757281553398, 8.040873045973026, 1.8321761186829812, 'HP:0000479', 'Abnormal retinal morphology'),
(730375, 'HP:0007950', 'Peripapillary chorioretinal atrophy', 'XPO:0128533', 'decreased size of the optic choroid vascular plexus', 0.5145631067961165, 11.854497839006713, 2.469794978848881, 'HP:0000610', 'Abnormal choroid morphology'),
(730376, 'HP:0007950', 'Peripapillary chorioretinal atrophy', 'XPO:0102581', 'abnormal outer limiting membrane morphology', 0.4174757281553398, 8.040873045973026, 1.8321761186829812, 'HP:0000479', 'Abnormal retinal morphology'),
(730377, 'HP:0007950', 'Peripapillary chorioretinal atrophy', 'XPO:0130265', 'increased size of the peripheral retina', 0.43, 8.040873045973026, 1.859455675666511, 'HP:0000479', 'Abnormal retinal morphology'),
(730378, 'HP:0007950', 'Peripapillary chorioretinal atrophy', 'XPO:0102017', 'abnormal retinal neural layer morphology', 0.4215686274509804, 8.040873045973026, 1.8411354685352277, 'HP:0000479', 'Abnormal retinal morphology'),
(730379, 'HP:0007950', 'Peripapillary chorioretinal atrophy', 'XPO:0103926', 'decreased pigmentation in the retinal pigmented epithelium', 0.4056603773584906, 8.040873045973026, 1.8060630094548564, 'HP:0000479', 'Abnormal retinal morphology'),
(730380, 'HP:0007950', 'Peripapillary chorioretinal atrophy', 'XPO:0100710', 'abnormal hyaloid vein', 0.45121951219512196, 9.463856994035337, 2.0664648403331274, 'HP:0008047', 'Abnormality of the vasculature of the eye'),
(730381, 'HP:0007950', 'Peripapillary chorioretinal atrophy', 'XPO:0101359', 'abnormal hyaloid artery', 0.44565217391304346, 9.463856994035337, 2.0536768107455488, 'HP:0008047', 'Abnormality of the vasculature of the eye'),
(730382, 'HP:0100904', 'Sclerosis of the middle phalanx of the 2nd finger', 'XPO:0102214', 'abnormal forelimb digit morphology', 0.44339622641509435, 7.492661022682715, 1.822695153684504, 'HP:0001167', 'Abnormal finger morphology'),
(730383, 'HP:0100904', 'Sclerosis of the middle phalanx of the 2nd finger', 'XPO:0115789', 'duplicated forelimb digit 5 in regenerating forelimb', 0.43846153846153846, 7.774297771301195, 1.8462747794580392, 'HP:0005918', 'Abnormal finger phalanx morphology'),
(730384, 'HP:0100904', 'Sclerosis of the middle phalanx of the 2nd finger', 'XPO:0141108', 'abnormally necrotic forelimb digit 2', 0.4017094017094017, 7.492661022682715, 1.734898376457027, 'HP:0001167', 'Abnormal finger morphology'),
(730385, 'HP:0100904', 'Sclerosis of the middle phalanx of the 2nd finger', 'XPO:0141556', 'abnormal forelimb digit morphology in the regenerating forelimb', 0.41964285714285715, 7.492661022682715, 1.7732009697610411, 'HP:0001167', 'Abnormal finger morphology'),
(730386, 'HP:0100904', 'Sclerosis of the middle phalanx of the 2nd finger', 'XPO:0103609', 'abnormally increased number of forelimb digit in the regenerating forelimb', 0.456, 7.774297771301195, 1.8828382255821516, 'HP:0005918', 'Abnormal finger phalanx morphology'),
(730387, 'HP:0100904', 'Sclerosis of the middle phalanx of the 2nd finger', 'XPO:0140716', 'abnormally necrotic forelimb digit 4', 0.4017094017094017, 7.492661022682715, 1.734898376457027, 'HP:0001167', 'Abnormal finger morphology'),
(730388, 'HP:0100904', 'Sclerosis of the middle phalanx of the 2nd finger', 'XPO:0115787', 'duplicated forelimb digit 3 in regenerating forelimb', 0.43846153846153846, 7.774297771301195, 1.8462747794580392, 'HP:0005918', 'Abnormal finger phalanx morphology'),
(730389, 'HP:0100904', 'Sclerosis of the middle phalanx of the 2nd finger', 'XPO:0103755', 'increased size of the forelimb digit', 0.4051724137931034, 7.492661022682715, 1.7423603393941962, 'HP:0001167', 'Abnormal finger morphology'),
(730390, 'HP:0100904', 'Sclerosis of the middle phalanx of the 2nd finger', 'XPO:0141143', 'abnormally necrotic forelimb digit 3', 0.4017094017094017, 7.492661022682715, 1.734898376457027, 'HP:0001167', 'Abnormal finger morphology'),
(730391, 'HP:0100904', 'Sclerosis of the middle phalanx of the 2nd finger', 'XPO:0102598', 'abnormal forelimb digit 3 morphology', 0.4351851851851852, 7.492661022682715, 1.8057394813997938, 'HP:0001167', 'Abnormal finger morphology'),
(730392, 'HP:0100904', 'Sclerosis of the middle phalanx of the 2nd finger', 'XPO:0140898', 'abnormally necrotic forelimb digit 5', 0.4017094017094017, 7.492661022682715, 1.734898376457027, 'HP:0001167', 'Abnormal finger morphology'),
(730393, 'HP:0100904', 'Sclerosis of the middle phalanx of the 2nd finger', 'XPO:0140219', 'abnormally necrotic forelimb digit', 0.41228070175438597, 7.492661022682715, 1.7575777491876043, 'HP:0001167', 'Abnormal finger morphology'),
(730394, 'HP:0100904', 'Sclerosis of the middle phalanx of the 2nd finger', 'XPO:0102529', 'abnormal forelimb digit 4 morphology', 0.4351851851851852, 7.492661022682715, 1.8057394813997938, 'HP:0001167', 'Abnormal finger morphology'),
(730395, 'HP:0100904', 'Sclerosis of the middle phalanx of the 2nd finger', 'XPO:0103634', 'abnormally increased number of forelimb digit', 0.4789915966386555, 7.774297771301195, 1.929721042591364, 'HP:0005918', 'Abnormal finger phalanx morphology'),
(730396, 'HP:0100904', 'Sclerosis of the middle phalanx of the 2nd finger', 'XPO:0102787', 'abnormal forelimb digit 5 morphology', 0.4351851851851852, 7.492661022682715, 1.8057394813997938, 'HP:0001167', 'Abnormal finger morphology'),
(730397, 'HP:0100904', 'Sclerosis of the middle phalanx of the 2nd finger', 'XPO:0115788', 'duplicated forelimb digit 4 in regenerating forelimb', 0.43846153846153846, 7.774297771301195, 1.8462747794580392, 'HP:0005918', 'Abnormal finger phalanx morphology'),
(730398, 'HP:0100904', 'Sclerosis of the middle phalanx of the 2nd finger', 'XPO:0103432', 'decreased size of the forelimb digit', 0.4017094017094017, 7.492661022682715, 1.734898376457027, 'HP:0001167', 'Abnormal finger morphology'),
(730399, 'HP:0100904', 'Sclerosis of the middle phalanx of the 2nd finger', 'XPO:0102746', 'abnormal forelimb digit 2 morphology', 0.4351851851851852, 7.492661022682715, 1.8057394813997938, 'HP:0001167', 'Abnormal finger morphology'),
(730400, 'HP:0100904', 'Sclerosis of the middle phalanx of the 2nd finger', 'XPO:0133358', 'fused forelimb digits', 0.40869565217391307, 7.492661022682715, 1.7499194219115835, 'HP:0001167', 'Abnormal finger morphology'),
(730401, 'HP:0100904', 'Sclerosis of the middle phalanx of the 2nd finger', 'XPO:0115786', 'duplicated forelimb digit 2 in regenerating forelimb', 0.43846153846153846, 7.774297771301195, 1.8462747794580392, 'HP:0005918', 'Abnormal finger phalanx morphology'),
(730402, 'HP:0033843', 'Postprandial fullness', 'XPO:0100215', 'abnormal first pancreatic bud', 0.4411764705882353, 5.05060299610679, 1.4927180591674907, 'HP:0025031', 'Abnormality of the digestive system'),
(730403, 'HP:0033843', 'Postprandial fullness', 'XPO:0100523', 'abnormal midgut', 0.4838709677419355, 5.05060299610679, 1.5632786569919361, 'HP:0025031', 'Abnormality of the digestive system'),
(730404, 'HP:0033843', 'Postprandial fullness', 'XPO:0126608', 'abnormally localised foregut', 0.42105263157894735, 5.05060299610679, 1.4582762710032966, 'HP:0025031', 'Abnormality of the digestive system'),
(730405, 'HP:0033843', 'Postprandial fullness', 'XPO:0107307', 'abnormal posterior hindgut endoderm', 0.42857142857142855, 5.05060299610679, 1.471238981671103, 'HP:0025031', 'Abnormality of the digestive system'),
(730406, 'HP:0033843', 'Postprandial fullness', 'XPO:0100493', 'abnormal liver and biliary system', 0.5172413793103449, 5.05060299610679, 1.6162861318637973, 'HP:0025031', 'Abnormality of the digestive system'),
(730407, 'HP:0033843', 'Postprandial fullness', 'XPO:0100216', 'abnormal hepato-pancreatic progenitor cell', 0.4166666666666667, 5.05060299610679, 1.45066119926208, 'HP:0025031', 'Abnormality of the digestive system'),
(730408, 'HP:0033843', 'Postprandial fullness', 'XPO:0107288', 'abnormal larval alimentary system', 0.5172413793103449, 5.05060299610679, 1.6162861318637973, 'HP:0025031', 'Abnormality of the digestive system'),
(730409, 'HP:0033843', 'Postprandial fullness', 'XPO:0100572', 'abnormal branchial arch', 0.40540540540540543, 5.05060299610679, 1.4309233924911664, 'HP:0025031', 'Abnormality of the digestive system'),
(730410, 'HP:0033843', 'Postprandial fullness', 'XPO:0142061', 'abnormal digestive tract morphology', 0.41025641025641024, 5.05060299610679, 1.4394590146346793, 'HP:0025031', 'Abnormality of the digestive system'),
(730411, 'HP:0033843', 'Postprandial fullness', 'XPO:0100718', 'abnormal ventral pancreatic bud', 0.45454545454545453, 5.05060299610679, 1.5151662069205463, 'HP:0025031', 'Abnormality of the digestive system'),
(730412, 'HP:0033843', 'Postprandial fullness', 'XPO:0100986', 'abnormal gut epithelium', 0.46875, 5.05060299610679, 1.5386585568036393, 'HP:0025031', 'Abnormality of the digestive system'),
(730413, 'HP:0033843', 'Postprandial fullness', 'XPO:0127393', 'abnormally localised pharyngeal cavity', 0.4444444444444444, 5.05060299610679, 1.4982364441950171, 'HP:0025031', 'Abnormality of the digestive system'),
(730414, 'HP:0033843', 'Postprandial fullness', 'XPO:0125663', 'absent oral evagination', 0.41025641025641024, 5.05060299610679, 1.4394590146346793, 'HP:0025031', 'Abnormality of the digestive system'),
(730415, 'HP:0033843', 'Postprandial fullness', 'XPO:0100890', 'abnormal pharyngeal cavity', 0.5, 5.05060299610679, 1.5891197242666757, 'HP:0025031', 'Abnormality of the digestive system'),
(730416, 'HP:0033843', 'Postprandial fullness', 'XPO:0131683', 'abnormal stomach epithelium', 0.4166666666666667, 5.05060299610679, 1.45066119926208, 'HP:0025031', 'Abnormality of the digestive system'),
(730417, 'HP:0033843', 'Postprandial fullness', 'XPO:0141717', 'abnormal tracheoesophageal fold', 0.42857142857142855, 5.05060299610679, 1.471238981671103, 'HP:0025031', 'Abnormality of the digestive system'),
(730418, 'HP:0033843', 'Postprandial fullness', 'XPO:0115495', 'abnormally protruding proctodeum', 0.45714285714285713, 5.05060299610679, 1.519489086480891, 'HP:0025031', 'Abnormality of the digestive system'),
(730419, 'HP:0033843', 'Postprandial fullness', 'XPO:0127721', 'abnormally localised manicotto glandulare', 0.41025641025641024, 5.05060299610679, 1.4394590146346793, 'HP:0025031', 'Abnormality of the digestive system'),
(730420, 'HP:0033843', 'Postprandial fullness', 'XPO:0141833', 'edematous alimentary system', 0.41025641025641024, 5.05060299610679, 1.4394590146346793, 'HP:0025031', 'Abnormality of the digestive system'),
(730421, 'HP:0033843', 'Postprandial fullness', 'XPO:0100621', 'abnormal peritoneum', 0.4411764705882353, 5.05060299610679, 1.4927180591674907, 'HP:0025031', 'Abnormality of the digestive system'),
(730422, 'HP:0033843', 'Postprandial fullness', 'XPO:0126499', 'abnormally localised liver and biliary system', 0.43243243243243246, 5.05060299610679, 1.4778513250178418, 'HP:0025031', 'Abnormality of the digestive system'),
(730423, 'HP:0033843', 'Postprandial fullness', 'XPO:0131673', 'abnormal buccopharyngeal membrane', 0.40540540540540543, 5.05060299610679, 1.4309233924911664, 'HP:0025031', 'Abnormality of the digestive system'),
(730424, 'HP:0033843', 'Postprandial fullness', 'XPO:0107305', 'abnormal dorsal posterior hindgut endoderm', 0.4166666666666667, 5.05060299610679, 1.45066119926208, 'HP:0025031', 'Abnormality of the digestive system'),
(730425, 'HP:0033843', 'Postprandial fullness', 'XPO:0101103', 'abnormal pharyngeal mesenchyme', 0.40540540540540543, 5.05060299610679, 1.4309233924911664, 'HP:0025031', 'Abnormality of the digestive system'),
(730426, 'HP:0033843', 'Postprandial fullness', 'XPO:0101601', 'abnormal proctodeum', 0.45454545454545453, 5.05060299610679, 1.5151662069205463, 'HP:0025031', 'Abnormality of the digestive system'),
(730427, 'HP:0033843', 'Postprandial fullness', 'XPO:0100486', 'abnormal oral evagination', 0.4838709677419355, 5.05060299610679, 1.5632786569919361, 'HP:0025031', 'Abnormality of the digestive system'),
(730428, 'HP:0033843', 'Postprandial fullness', 'XPO:0115392', 'abnormally incomplete structure of alimentary system', 0.42105263157894735, 5.05060299610679, 1.4582762710032966, 'HP:0025031', 'Abnormality of the digestive system'),
(730429, 'HP:0033843', 'Postprandial fullness', 'XPO:0107308', 'abnormal anterior hindgut endoderm', 0.42857142857142855, 5.05060299610679, 1.471238981671103, 'HP:0025031', 'Abnormality of the digestive system'),
(730430, 'HP:0033843', 'Postprandial fullness', 'XPO:0131662', 'abnormal foregut epithelium', 0.4166666666666667, 5.05060299610679, 1.45066119926208, 'HP:0025031', 'Abnormality of the digestive system'),
(730431, 'HP:0033843', 'Postprandial fullness', 'XPO:0100893', 'abnormal hyoid arch', 0.40540540540540543, 5.05060299610679, 1.4309233924911664, 'HP:0025031', 'Abnormality of the digestive system'),
(730432, 'HP:0033843', 'Postprandial fullness', 'XPO:0126837', 'abnormally localised midgut', 0.42105263157894735, 5.05060299610679, 1.4582762710032966, 'HP:0025031', 'Abnormality of the digestive system'),
(730433, 'HP:0033843', 'Postprandial fullness', 'XPO:0126425', 'abnormally localised posterior foregut', 0.41025641025641024, 5.05060299610679, 1.4394590146346793, 'HP:0025031', 'Abnormality of the digestive system'),
(730434, 'HP:0033843', 'Postprandial fullness', 'XPO:0100454', 'abnormal lung bud', 0.40540540540540543, 5.05060299610679, 1.4309233924911664, 'HP:0025031', 'Abnormality of the digestive system'),
(730435, 'HP:0033843', 'Postprandial fullness', 'XPO:0100494', 'abnormal liver diverticulum', 0.40540540540540543, 5.05060299610679, 1.4309233924911664, 'HP:0025031', 'Abnormality of the digestive system'),
(730436, 'HP:0033843', 'Postprandial fullness', 'XPO:0101381', 'abnormal ventral foregut', 0.46875, 5.05060299610679, 1.5386585568036393, 'HP:0025031', 'Abnormality of the digestive system'),
(730437, 'HP:0033843', 'Postprandial fullness', 'XPO:0126520', 'abnormally localised hindgut', 0.42105263157894735, 5.05060299610679, 1.4582762710032966, 'HP:0025031', 'Abnormality of the digestive system'),
(730438, 'HP:0033843', 'Postprandial fullness', 'XPO:0100130', 'abnormal mouth primordium', 0.4166666666666667, 5.05060299610679, 1.45066119926208, 'HP:0025031', 'Abnormality of the digestive system'),
(730439, 'HP:0033843', 'Postprandial fullness', 'XPO:0101377', 'abnormal manicotto glandulare', 0.4838709677419355, 5.05060299610679, 1.5632786569919361, 'HP:0025031', 'Abnormality of the digestive system'),
(730440, 'HP:0033843', 'Postprandial fullness', 'XPO:0101198', 'abnormal digestive enzyme secreting cell', 0.4411764705882353, 5.05060299610679, 1.4927180591674907, 'HP:0025031', 'Abnormality of the digestive system'),
(730441, 'HP:0033843', 'Postprandial fullness', 'XPO:0101021', 'abnormal dorsal foregut', 0.46875, 5.05060299610679, 1.5386585568036393, 'HP:0025031', 'Abnormality of the digestive system'),
(730442, 'HP:0033843', 'Postprandial fullness', 'XPO:0126466', 'abnormally localised alimentary system', 0.4444444444444444, 5.05060299610679, 1.4982364441950171, 'HP:0025031', 'Abnormality of the digestive system'),
(730443, 'HP:0033843', 'Postprandial fullness', 'XPO:0100188', 'abnormal delta cell', 0.40540540540540543, 5.05060299610679, 1.4309233924911664, 'HP:0025031', 'Abnormality of the digestive system'),
(730444, 'HP:0033843', 'Postprandial fullness', 'XPO:0125745', 'absent pharyngeal cavity', 0.43243243243243246, 5.05060299610679, 1.4778513250178418, 'HP:0025031', 'Abnormality of the digestive system'),
(730445, 'HP:0033843', 'Postprandial fullness', 'XPO:0107306', 'abnormal ventral posterior hindgut endoderm', 0.4166666666666667, 5.05060299610679, 1.45066119926208, 'HP:0025031', 'Abnormality of the digestive system'),
(730446, 'HP:0033843', 'Postprandial fullness', 'XPO:0101784', 'abnormal alimentary system morphology', 0.43243243243243246, 5.05060299610679, 1.4778513250178418, 'HP:0025031', 'Abnormality of the digestive system'),
(730447, 'HP:0033843', 'Postprandial fullness', 'XPO:0127678', 'abnormally localised ventral foregut', 0.41025641025641024, 5.05060299610679, 1.4394590146346793, 'HP:0025031', 'Abnormality of the digestive system'),
(730448, 'HP:0033843', 'Postprandial fullness', 'XPO:0102125', 'abnormal liver and biliary system morphology', 0.41025641025641024, 5.05060299610679, 1.4394590146346793, 'HP:0025031', 'Abnormality of the digestive system'),
(730449, 'HP:0033843', 'Postprandial fullness', 'XPO:0127838', 'abnormally localised dorsal foregut', 0.41025641025641024, 5.05060299610679, 1.4394590146346793, 'HP:0025031', 'Abnormality of the digestive system'),
(730450, 'HP:0033843', 'Postprandial fullness', 'XPO:0126705', 'abnormally localised larval alimentary system', 0.42105263157894735, 5.05060299610679, 1.4582762710032966, 'HP:0025031', 'Abnormality of the digestive system'),
(730451, 'HP:0033843', 'Postprandial fullness', 'XPO:0100591', 'abnormal pharyngeal arch', 0.4166666666666667, 5.05060299610679, 1.45066119926208, 'HP:0025031', 'Abnormality of the digestive system'),
(730452, 'HP:0033843', 'Postprandial fullness', 'XPO:0100462', 'abnormal anterior foregut', 0.46875, 5.05060299610679, 1.5386585568036393, 'HP:0025031', 'Abnormality of the digestive system'),
(730453, 'HP:0033843', 'Postprandial fullness', 'XPO:0142027', 'abnormally localised digestive tract', 0.42105263157894735, 5.05060299610679, 1.4582762710032966, 'HP:0025031', 'Abnormality of the digestive system'),
(730454, 'HP:0033843', 'Postprandial fullness', 'XPO:0142054', 'abnormal digestive tract', 0.5, 5.05060299610679, 1.5891197242666757, 'HP:0025031', 'Abnormality of the digestive system'),
(730455, 'HP:0033843', 'Postprandial fullness', 'XPO:0125084', 'absent larval alimentary system', 0.41025641025641024, 5.05060299610679, 1.4394590146346793, 'HP:0025031', 'Abnormality of the digestive system'),
(730456, 'HP:0033843', 'Postprandial fullness', 'XPO:0124857', 'absent alimentary system', 0.43243243243243246, 5.05060299610679, 1.4778513250178418, 'HP:0025031', 'Abnormality of the digestive system'),
(730457, 'HP:0033843', 'Postprandial fullness', 'XPO:0115391', 'abnormally undifferentiated alimentary system', 0.5172413793103449, 5.05060299610679, 1.6162861318637973, 'HP:0025031', 'Abnormality of the digestive system'),
(730458, 'HP:0033843', 'Postprandial fullness', 'XPO:0100156', 'abnormal foregut', 0.4838709677419355, 5.05060299610679, 1.5632786569919361, 'HP:0025031', 'Abnormality of the digestive system'),
(730459, 'HP:0033843', 'Postprandial fullness', 'XPO:0107375', 'abnormal larval alimentary system morphology', 0.41025641025641024, 5.05060299610679, 1.4394590146346793, 'HP:0025031', 'Abnormality of the digestive system'),
(730460, 'HP:0033843', 'Postprandial fullness', 'XPO:0142020', 'absent digestive tract', 0.41025641025641024, 5.05060299610679, 1.4394590146346793, 'HP:0025031', 'Abnormality of the digestive system'),
(730461, 'HP:0033843', 'Postprandial fullness', 'XPO:0107304', 'abnormal hindgut endoderm', 0.4411764705882353, 5.05060299610679, 1.4927180591674907, 'HP:0025031', 'Abnormality of the digestive system'),
(730462, 'HP:0033843', 'Postprandial fullness', 'XPO:0101101', 'abnormal posterior foregut', 0.46875, 5.05060299610679, 1.5386585568036393, 'HP:0025031', 'Abnormality of the digestive system'),
(730463, 'HP:0033843', 'Postprandial fullness', 'XPO:0101169', 'abnormal hepato-pancreatic duct', 0.45454545454545453, 5.05060299610679, 1.5151662069205463, 'HP:0025031', 'Abnormality of the digestive system'),
(730464, 'HP:0033843', 'Postprandial fullness', 'XPO:0127173', 'abnormally localised anterior foregut', 0.41025641025641024, 5.05060299610679, 1.4394590146346793, 'HP:0025031', 'Abnormality of the digestive system'),
(730465, 'HP:0033843', 'Postprandial fullness', 'XPO:0100492', 'abnormal gall bladder primordium', 0.4411764705882353, 5.05060299610679, 1.4927180591674907, 'HP:0025031', 'Abnormality of the digestive system'),
(730466, 'HP:0033843', 'Postprandial fullness', 'XPO:0100214', 'abnormal second pancreatic bud', 0.42857142857142855, 5.05060299610679, 1.471238981671103, 'HP:0025031', 'Abnormality of the digestive system'),
(730467, 'HP:0033843', 'Postprandial fullness', 'XPO:0102522', 'abnormal pharyngeal cavity morphology', 0.43243243243243246, 5.05060299610679, 1.4778513250178418, 'HP:0025031', 'Abnormality of the digestive system'),
(730468, 'HP:0033843', 'Postprandial fullness', 'XPO:0101084', 'abnormal mesentery', 0.40540540540540543, 5.05060299610679, 1.4309233924911664, 'HP:0025031', 'Abnormality of the digestive system'),
(730469, 'HP:0033843', 'Postprandial fullness', 'XPO:0127307', 'abnormally localised oral evagination', 0.42105263157894735, 5.05060299610679, 1.4582762710032966, 'HP:0025031', 'Abnormality of the digestive system'),
(730470, 'HP:0033843', 'Postprandial fullness', 'XPO:0100735', 'abnormal hindgut', 0.4838709677419355, 5.05060299610679, 1.5632786569919361, 'HP:0025031', 'Abnormality of the digestive system'),
(730471, 'HP:0033843', 'Postprandial fullness', 'XPO:0100152', 'abnormal alimentary system', 0.5357142857142857, 5.05060299610679, 1.6448951870820767, 'HP:0025031', 'Abnormality of the digestive system'),
(730472, 'HP:0033843', 'Postprandial fullness', 'XPO:0124888', 'absent liver and biliary system', 0.42105263157894735, 5.05060299610679, 1.4582762710032966, 'HP:0025031', 'Abnormality of the digestive system'),
(730473, 'HP:0011003', 'High myopia', 'XPO:0127803', 'abnormally localised retinal layer', 0.4074074074074074, 6.02624522851634, 1.5668876618797856, 'HP:0000478', 'Abnormality of the eye'),
(730474, 'HP:0011003', 'High myopia', 'XPO:0100727', 'abnormal odontogenic papilla', 0.40540540540540543, 3.868794716113063, 1.2523698696136485, 'UPHENO:0002844', 'abnormal head'),
(730475, 'HP:0011003', 'High myopia', 'XPO:0100844', 'abnormal lens transitional zone', 0.4117647058823529, 6.02624522851634, 1.5752444553449358, 'HP:0000478', 'Abnormality of the eye'),
(730476, 'HP:0011003', 'High myopia', 'XPO:0101390', 'abnormal ciliary body', 0.4117647058823529, 6.02624522851634, 1.5752444553449358, 'HP:0000478', 'Abnormality of the eye'),
(730477, 'HP:0011003', 'High myopia', 'XPO:0101416', 'abnormal cornea', 0.42, 6.02624522851634, 1.590918915588366, 'HP:0000478', 'Abnormality of the eye'),
(730478, 'HP:0011003', 'High myopia', 'XPO:0101554', 'abnormal peripheral retina', 0.42, 6.02624522851634, 1.590918915588366, 'HP:0000478', 'Abnormality of the eye'),
(730479, 'HP:0011003', 'High myopia', 'XPO:0101289', 'abnormal orbital region', 0.41304347826086957, 5.757493499662858, 1.5421073701805246, 'HP:0000315', 'Abnormality of the orbital region'),
(730480, 'HP:0011003', 'High myopia', 'XPO:0142052', 'abnormal nasal region', 0.4166666666666667, 3.868794716113063, 1.2696447528267278, 'UPHENO:0002844', 'abnormal head'),
(730481, 'HP:0011003', 'High myopia', 'XPO:0100881', 'abnormal sclera', 0.42857142857142855, 6.02624522851634, 1.6070707907578319, 'HP:0000478', 'Abnormality of the eye'),
(730482, 'HP:0011003', 'High myopia', 'XPO:0100918', 'abnormal lens', 0.42857142857142855, 6.02624522851634, 1.6070707907578319, 'HP:0000478', 'Abnormality of the eye'),
(730483, 'HP:0011003', 'High myopia', 'XPO:0101173', 'abnormal retinal layer', 0.4666666666666667, 6.02624522851634, 1.6769757819681315, 'HP:0000478', 'Abnormality of the eye'),
(730484, 'HP:0011003', 'High myopia', 'XPO:0101578', 'abnormal pupil', 0.42, 6.02624522851634, 1.590918915588366, 'HP:0000478', 'Abnormality of the eye'),
(730485, 'HP:0011003', 'High myopia', 'XPO:0100485', 'abnormal retina', 0.42857142857142855, 6.02624522851634, 1.6070707907578319, 'HP:0000478', 'Abnormality of the eye'),
(730486, 'HP:0011003', 'High myopia', 'XPO:0100002', 'abnormal head', 0.4166666666666667, 3.868794716113063, 1.2696447528267278, 'UPHENO:0002844', 'abnormal head'),
(730487, 'HP:0011003', 'High myopia', 'XPO:0100627', 'abnormal pharyngeal region', 0.40540540540540543, 3.868794716113063, 1.2523698696136485, 'UPHENO:0002844', 'abnormal head'),
(730488, 'HP:0011003', 'High myopia', 'XPO:0100564', 'abnormal central retina', 0.42, 6.02624522851634, 1.590918915588366, 'HP:0000478', 'Abnormality of the eye'),
(730489, 'HP:0011003', 'High myopia', 'XPO:0101230', 'abnormal iris', 0.4117647058823529, 6.02624522851634, 1.5752444553449358, 'HP:0000478', 'Abnormality of the eye'),
(730490, 'HP:0030312', 'Obliteration of the calvarial diploe', 'XPO:0130767', 'increased size of the orbital region', 0.44285714285714284, 7.024697770424301, 1.7637850163909, 'HP:0000929', 'Abnormal skull morphology'),
(730491, 'HP:0030312', 'Obliteration of the calvarial diploe', 'XPO:0140914', 'abnormally necrotic intercanthal region', 0.42, 4.5318002188002176, 1.3796217205799897, 'UPHENO:0087907', 'abnormal head morphology'),
(730492, 'HP:0030312', 'Obliteration of the calvarial diploe', 'XPO:0103721', 'increased size of the chondrocranium', 0.4262295081967213, 4.638757693672553, 1.4061206955371255, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(730493, 'HP:0030312', 'Obliteration of the calvarial diploe', 'XPO:0140926', 'abnormally necrotic neurocranium', 0.5254237288135594, 7.024697770424301, 1.9211826816637279, 'HP:0000929', 'Abnormal skull morphology'),
(730494, 'HP:0030312', 'Obliteration of the calvarial diploe', 'XPO:0102272', 'abnormal notochordal sheath morphology', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(730495, 'HP:0030312', 'Obliteration of the calvarial diploe', 'XPO:0140132', 'abnormally necrotic ethmoid region', 0.45614035087719296, 4.638757693672553, 1.4546217934659431, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(730496, 'HP:0030312', 'Obliteration of the calvarial diploe', 'XPO:0141201', 'abnormally necrotic sphenoid region', 0.5254237288135594, 7.024697770424301, 1.9211826816637279, 'HP:0000929', 'Abnormal skull morphology'),
(730497, 'HP:0030312', 'Obliteration of the calvarial diploe', 'XPO:0101634', 'abnormal head morphology', 0.4666666666666667, 4.5318002188002176, 1.4542489821577214, 'UPHENO:0087907', 'abnormal head morphology'),
(730498, 'HP:0030312', 'Obliteration of the calvarial diploe', 'XPO:0102485', 'abnormal osseous labyrinth morphology', 0.4189189189189189, 7.024697770424301, 1.7154529418548001, 'HP:0000929', 'Abnormal skull morphology'),
(730499, 'HP:0030312', 'Obliteration of the calvarial diploe', 'XPO:0128880', 'decreased size of the lower jaw', 0.41333333333333333, 7.024697770424301, 1.7039782114536297, 'HP:0000929', 'Abnormal skull morphology'),
(730500, 'HP:0030312', 'Obliteration of the calvarial diploe', 'XPO:0139880', 'abnormally necrotic dermatocranium', 0.4406779661016949, 4.638757693672553, 1.4297546312868548, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(730501, 'HP:0030312', 'Obliteration of the calvarial diploe', 'XPO:0129790', 'increased size of the mandibular arch skeleton', 0.40625, 4.638757693672553, 1.3727692133255593, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(730502, 'HP:0030312', 'Obliteration of the calvarial diploe', 'XPO:0139784', 'abnormally necrotic cranium', 0.4642857142857143, 4.638757693672553, 1.4675520192501232, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(730503, 'HP:0030312', 'Obliteration of the calvarial diploe', 'XPO:0102144', 'abnormal cranial skeleton morphology', 0.4117647058823529, 6.211345574613551, 1.599253852164941, 'UPHENO:0087089', 'abnormal axial skeleton plus cranial skeleton morphology'),
(730504, 'HP:0030312', 'Obliteration of the calvarial diploe', 'XPO:0129688', 'increased size of the olfactory region', 0.5081967213114754, 7.024697770424301, 1.8894254087244782, 'HP:0000929', 'Abnormal skull morphology'),
(730505, 'HP:0030312', 'Obliteration of the calvarial diploe', 'XPO:0101957', 'abnormal axial skeleton morphology', 0.42, 6.211345574613551, 1.61516721776344, 'UPHENO:0087089', 'abnormal axial skeleton plus cranial skeleton morphology'),
(730506, 'HP:0030312', 'Obliteration of the calvarial diploe', 'XPO:0102795', 'abnormal branchial basket morphology', 0.4126984126984127, 4.638757693672553, 1.3836213127410304, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(730507, 'HP:0030312', 'Obliteration of the calvarial diploe', 'XPO:0102720', 'abnormal dermatocranium morphology', 0.49056603773584906, 4.638757693672553, 1.508514826510376, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(730508, 'HP:0030312', 'Obliteration of the calvarial diploe', 'XPO:0100420', 'abnormal choana', 0.4528301886792453, 4.5318002188002176, 1.4325278175784049, 'UPHENO:0087907', 'abnormal head morphology'),
(730509, 'HP:0030312', 'Obliteration of the calvarial diploe', 'XPO:0130383', 'increased size of the occipital region', 0.5166666666666667, 7.024697770424301, 1.9051055564944135, 'HP:0000929', 'Abnormal skull morphology'),
(730510, 'HP:0030312', 'Obliteration of the calvarial diploe', 'XPO:0102097', 'abnormal skeletal system morphology', 0.4444444444444444, 4.638757693672553, 1.4358516936218344, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(730511, 'HP:0030312', 'Obliteration of the calvarial diploe', 'XPO:0128208', 'decreased size of the olfactory region', 0.5081967213114754, 7.024697770424301, 1.8894254087244782, 'HP:0000929', 'Abnormal skull morphology'),
(730512, 'HP:0030312', 'Obliteration of the calvarial diploe', 'XPO:0141061', 'abnormally necrotic suspensorium', 0.4482758620689655, 4.638757693672553, 1.4420274283314136, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(730513, 'HP:0030312', 'Obliteration of the calvarial diploe', 'XPO:0103358', 'decreased size of the pharyngeal region', 0.42857142857142855, 4.5318002188002176, 1.3936283915633758, 'UPHENO:0087907', 'abnormal head morphology'),
(730514, 'HP:0030312', 'Obliteration of the calvarial diploe', 'XPO:0115526', 'abnormally incomplete structure of head', 0.45652173913043476, 4.5318002188002176, 1.4383550734357495, 'UPHENO:0087907', 'abnormal head morphology'),
(730515, 'HP:0030312', 'Obliteration of the calvarial diploe', 'XPO:0102564', 'abnormal olfactory region morphology', 0.5740740740740741, 7.024697770424301, 2.008157580521644, 'HP:0000929', 'Abnormal skull morphology'),
(730516, 'HP:0030312', 'Obliteration of the calvarial diploe', 'XPO:0129718', 'increased size of the ethmoid region', 0.4406779661016949, 4.638757693672553, 1.4297546312868548, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(730517, 'HP:0030312', 'Obliteration of the calvarial diploe', 'XPO:0103739', 'increased size of the pharyngeal region', 0.42857142857142855, 4.5318002188002176, 1.3936283915633758, 'UPHENO:0087907', 'abnormal head morphology'),
(730518, 'HP:0030312', 'Obliteration of the calvarial diploe', 'XPO:0141339', 'decreased pigmentation in the head', 0.4375, 4.5318002188002176, 1.4080705222839853, 'UPHENO:0087907', 'abnormal head morphology'),
(730519, 'HP:0030312', 'Obliteration of the calvarial diploe', 'XPO:0131638', 'increased size of the intercanthal region', 0.40384615384615385, 4.5318002188002176, 1.3528303989641963, 'UPHENO:0087907', 'abnormal head morphology'),
(730520, 'HP:0030312', 'Obliteration of the calvarial diploe', 'XPO:0102401', 'abnormal neurocranium morphology', 0.5740740740740741, 7.024697770424301, 2.008157580521644, 'HP:0000929', 'Abnormal skull morphology'),
(730521, 'HP:0030312', 'Obliteration of the calvarial diploe', 'XPO:0141835', 'edematous head', 0.44680851063829785, 4.5318002188002176, 1.422971154406314, 'UPHENO:0087907', 'abnormal head morphology'),
(730522, 'HP:0030312', 'Obliteration of the calvarial diploe', 'XPO:0102082', 'abnormal circumpharyngeal ridge morphology', 0.42857142857142855, 4.5318002188002176, 1.3936283915633758, 'UPHENO:0087907', 'abnormal head morphology'),
(730523, 'HP:0030312', 'Obliteration of the calvarial diploe', 'XPO:0128947', 'decreased size of the otic region', 0.5081967213114754, 7.024697770424301, 1.8894254087244782, 'HP:0000929', 'Abnormal skull morphology'),
(730524, 'HP:0030312', 'Obliteration of the calvarial diploe', 'XPO:0129514', 'increased size of the cranium', 0.4482758620689655, 4.638757693672553, 1.4420274283314136, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(730525, 'HP:0030312', 'Obliteration of the calvarial diploe', 'XPO:0128971', 'decreased size of the fenestra subocularis', 0.45614035087719296, 4.638757693672553, 1.4546217934659431, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(730526, 'HP:0030312', 'Obliteration of the calvarial diploe', 'XPO:0115586', 'abnormally decreased volume of chondrocranium', 0.4126984126984127, 4.638757693672553, 1.3836213127410304, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(730527, 'HP:0030312', 'Obliteration of the calvarial diploe', 'XPO:0141839', 'edematous pharyngeal region', 0.45652173913043476, 4.5318002188002176, 1.4383550734357495, 'UPHENO:0087907', 'abnormal head morphology'),
(730528, 'HP:0030312', 'Obliteration of the calvarial diploe', 'XPO:0102828', 'abnormal occipital region morphology', 0.5849056603773585, 7.024697770424301, 2.027013933933702, 'HP:0000929', 'Abnormal skull morphology'),
(730529, 'HP:0030312', 'Obliteration of the calvarial diploe', 'XPO:0102054', 'abnormal notochord morphology', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(730530, 'HP:0030312', 'Obliteration of the calvarial diploe', 'XPO:0128477', 'decreased size of the neurocranium', 0.5, 7.024697770424301, 1.8741261657669024, 'HP:0000929', 'Abnormal skull morphology'),
(730531, 'HP:0030312', 'Obliteration of the calvarial diploe', 'XPO:0129957', 'increased size of the neurocranium', 0.5, 7.024697770424301, 1.8741261657669024, 'HP:0000929', 'Abnormal skull morphology'),
(730532, 'HP:0030312', 'Obliteration of the calvarial diploe', 'XPO:0101681', 'abnormal chondrocranium morphology', 0.49056603773584906, 4.638757693672553, 1.508514826510376, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(730533, 'HP:0030312', 'Obliteration of the calvarial diploe', 'XPO:0128310', 'decreased size of the mandibular arch skeleton', 0.40625, 4.638757693672553, 1.3727692133255593, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(730534, 'HP:0030312', 'Obliteration of the calvarial diploe', 'XPO:0103176', 'abnormal fenestra basicranialis morphology', 0.5, 4.638757693672553, 1.5229507040072823, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(730535, 'HP:0030312', 'Obliteration of the calvarial diploe', 'XPO:0140897', 'abnormally necrotic lower jaw', 0.4246575342465753, 7.024697770424301, 1.727162654186281, 'HP:0000929', 'Abnormal skull morphology'),
(730536, 'HP:0030312', 'Obliteration of the calvarial diploe', 'XPO:0102052', 'abnormal choana morphology', 0.5254237288135594, 7.024697770424301, 1.9211826816637279, 'HP:0000929', 'Abnormal skull morphology'),
(730537, 'HP:0030312', 'Obliteration of the calvarial diploe', 'XPO:0102215', 'abnormal mandibular arch skeleton morphology', 0.4642857142857143, 4.638757693672553, 1.4675520192501232, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(730538, 'HP:0030312', 'Obliteration of the calvarial diploe', 'XPO:0102351', 'abnormal sphenoid region morphology', 0.5740740740740741, 7.024697770424301, 2.008157580521644, 'HP:0000929', 'Abnormal skull morphology'),
(730539, 'HP:0030312', 'Obliteration of the calvarial diploe', 'XPO:0128291', 'decreased size of the dermatocranium', 0.4262295081967213, 4.638757693672553, 1.4061206955371255, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(730540, 'HP:0030312', 'Obliteration of the calvarial diploe', 'XPO:0130062', 'increased size of the head region', 0.40384615384615385, 4.5318002188002176, 1.3528303989641963, 'UPHENO:0087907', 'abnormal head morphology'),
(730541, 'HP:0030312', 'Obliteration of the calvarial diploe', 'XPO:0129291', 'decreased size of the orbital region', 0.44285714285714284, 7.024697770424301, 1.7637850163909, 'HP:0000929', 'Abnormal skull morphology'),
(730542, 'HP:0030312', 'Obliteration of the calvarial diploe', 'XPO:0101860', 'abnormal skeletal subdivision morphology', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(730543, 'HP:0030312', 'Obliteration of the calvarial diploe', 'XPO:0128034', 'decreased size of the cranium', 0.4482758620689655, 4.638757693672553, 1.4420274283314136, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(730544, 'HP:0030312', 'Obliteration of the calvarial diploe', 'XPO:0102567', 'abnormal skeleton morphology', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(730545, 'HP:0030312', 'Obliteration of the calvarial diploe', 'XPO:0128905', 'decreased size of the occipital region', 0.5166666666666667, 7.024697770424301, 1.9051055564944135, 'HP:0000929', 'Abnormal skull morphology'),
(730546, 'HP:0030312', 'Obliteration of the calvarial diploe', 'XPO:0102092', 'abnormal ethmoid region morphology', 0.5, 4.638757693672553, 1.5229507040072823, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(730547, 'HP:0030312', 'Obliteration of the calvarial diploe', 'XPO:0101997', 'abnormal braincase and otic capsule skeleton morphology', 0.4727272727272727, 4.638757693672553, 1.4808333037085841, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(730548, 'HP:0030312', 'Obliteration of the calvarial diploe', 'XPO:0130358', 'increased size of the lower jaw', 0.41333333333333333, 7.024697770424301, 1.7039782114536297, 'HP:0000929', 'Abnormal skull morphology'),
(730549, 'HP:0030312', 'Obliteration of the calvarial diploe', 'XPO:0139745', 'abnormally necrotic chondrocranium', 0.4406779661016949, 4.638757693672553, 1.4297546312868548, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(730550, 'HP:0030312', 'Obliteration of the calvarial diploe', 'XPO:0130324', 'increased size of the choana', 0.47692307692307695, 7.024697770424301, 1.8303662133915815, 'HP:0000929', 'Abnormal skull morphology'),
(730551, 'HP:0030312', 'Obliteration of the calvarial diploe', 'XPO:0129225', 'decreased size of the upper jaw', 0.4025974025974026, 7.024697770424301, 1.6817030286006471, 'HP:0000929', 'Abnormal skull morphology'),
(730552, 'HP:0030312', 'Obliteration of the calvarial diploe', 'XPO:0139775', 'abnormally necrotic braincase and otic capsule skeleton', 0.4262295081967213, 4.638757693672553, 1.4061206955371255, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(730553, 'HP:0030312', 'Obliteration of the calvarial diploe', 'XPO:0128668', 'decreased size of the fenestra basicranialis', 0.45614035087719296, 4.638757693672553, 1.4546217934659431, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(730554, 'HP:0030312', 'Obliteration of the calvarial diploe', 'XPO:0140644', 'abnormally necrotic otic region', 0.5254237288135594, 7.024697770424301, 1.9211826816637279, 'HP:0000929', 'Abnormal skull morphology'),
(730555, 'HP:0030312', 'Obliteration of the calvarial diploe', 'XPO:0103381', 'increased size of the head', 0.543859649122807, 7.024697770424301, 1.9545970594004087, 'HP:0000929', 'Abnormal skull morphology'),
(730556, 'HP:0030312', 'Obliteration of the calvarial diploe', 'XPO:0141719', 'abnormal anterior notochord morphology', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(730557, 'HP:0030312', 'Obliteration of the calvarial diploe', 'XPO:0102921', 'abnormal orbital region morphology', 0.5081967213114754, 7.024697770424301, 1.8894254087244782, 'HP:0000929', 'Abnormal skull morphology'),
(730558, 'HP:0030312', 'Obliteration of the calvarial diploe', 'XPO:0102010', 'abnormal perichondrium morphology', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(730559, 'HP:0030312', 'Obliteration of the calvarial diploe', 'XPO:0101764', 'abnormal cranium morphology', 0.5098039215686274, 4.638757693672553, 1.5378091115092631, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(730560, 'HP:0030312', 'Obliteration of the calvarial diploe', 'XPO:0141298', 'abnormal intercanthal region morphology', 0.44680851063829785, 4.5318002188002176, 1.422971154406314, 'UPHENO:0087907', 'abnormal head morphology'),
(730561, 'HP:0030312', 'Obliteration of the calvarial diploe', 'XPO:0128659', 'decreased size of the braincase and otic capsule skeleton', 0.4126984126984127, 4.638757693672553, 1.3836213127410304, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(730562, 'HP:0030312', 'Obliteration of the calvarial diploe', 'XPO:0141193', 'abnormally necrotic mandibular arch skeleton', 0.41935483870967744, 4.638757693672553, 1.394734915474381, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(730563, 'HP:0030312', 'Obliteration of the calvarial diploe', 'XPO:0102776', 'abnormal fenestra subocularis morphology', 0.5, 4.638757693672553, 1.5229507040072823, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(730564, 'HP:0030312', 'Obliteration of the calvarial diploe', 'XPO:0128209', 'decreased size of the sphenoid region', 0.5081967213114754, 7.024697770424301, 1.8894254087244782, 'HP:0000929', 'Abnormal skull morphology'),
(730565, 'HP:0030312', 'Obliteration of the calvarial diploe', 'XPO:0102259', 'abnormal pharyngeal region morphology', 0.4772727272727273, 4.5318002188002176, 1.4706816956370683, 'UPHENO:0087907', 'abnormal head morphology'),
(730566, 'HP:0030312', 'Obliteration of the calvarial diploe', 'XPO:0102804', 'abnormal pharyngeal pouch morphology', 0.4375, 4.5318002188002176, 1.4080705222839853, 'UPHENO:0087907', 'abnormal head morphology'),
(730567, 'HP:0030312', 'Obliteration of the calvarial diploe', 'XPO:0128846', 'decreased size of the choana', 0.47692307692307695, 7.024697770424301, 1.8303662133915815, 'HP:0000929', 'Abnormal skull morphology'),
(730568, 'HP:0030312', 'Obliteration of the calvarial diploe', 'XPO:0103707', 'increased pigmentation in the head', 0.4375, 4.5318002188002176, 1.4080705222839853, 'UPHENO:0087907', 'abnormal head morphology'),
(730569, 'HP:0030312', 'Obliteration of the calvarial diploe', 'XPO:0130425', 'increased size of the otic region', 0.5081967213114754, 7.024697770424301, 1.8894254087244782, 'HP:0000929', 'Abnormal skull morphology'),
(730570, 'HP:0030312', 'Obliteration of the calvarial diploe', 'XPO:0139832', 'abnormally necrotic splanchnocranium', 0.4406779661016949, 4.638757693672553, 1.4297546312868548, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(730571, 'HP:0030312', 'Obliteration of the calvarial diploe', 'XPO:0103101', 'abnormal medial nasal prominence morphology', 0.4375, 4.5318002188002176, 1.4080705222839853, 'UPHENO:0087907', 'abnormal head morphology'),
(730572, 'HP:0030312', 'Obliteration of the calvarial diploe', 'XPO:0102217', 'abnormal elastica externa morphology', 0.4444444444444444, 4.638757693672553, 1.4358516936218344, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(730573, 'HP:0030312', 'Obliteration of the calvarial diploe', 'XPO:0128033', 'decreased size of the splanchnocranium', 0.4262295081967213, 4.638757693672553, 1.4061206955371255, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(730574, 'HP:0030312', 'Obliteration of the calvarial diploe', 'XPO:0129689', 'increased size of the sphenoid region', 0.5081967213114754, 7.024697770424301, 1.8894254087244782, 'HP:0000929', 'Abnormal skull morphology'),
(730575, 'HP:0030312', 'Obliteration of the calvarial diploe', 'XPO:0130138', 'increased size of the braincase and otic capsule skeleton', 0.4126984126984127, 4.638757693672553, 1.3836213127410304, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(730576, 'HP:0030312', 'Obliteration of the calvarial diploe', 'XPO:0102216', 'abnormal vertebral column morphology', 0.41818181818181815, 6.272837960958401, 1.6196255072310737, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(730577, 'HP:0030312', 'Obliteration of the calvarial diploe', 'XPO:0130701', 'increased size of the upper jaw', 0.4025974025974026, 7.024697770424301, 1.6817030286006471, 'HP:0000929', 'Abnormal skull morphology'),
(730578, 'HP:0030312', 'Obliteration of the calvarial diploe', 'XPO:0128238', 'decreased size of the ethmoid region', 0.4406779661016949, 4.638757693672553, 1.4297546312868548, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(730579, 'HP:0030312', 'Obliteration of the calvarial diploe', 'XPO:0102538', 'abnormal lateral nasal prominence morphology', 0.4375, 4.5318002188002176, 1.4080705222839853, 'UPHENO:0087907', 'abnormal head morphology'),
(730580, 'HP:0030312', 'Obliteration of the calvarial diploe', 'XPO:0129513', 'increased size of the splanchnocranium', 0.4262295081967213, 4.638757693672553, 1.4061206955371255, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(730581, 'HP:0030312', 'Obliteration of the calvarial diploe', 'XPO:0102461', 'abnormal postcranial axial skeleton morphology', 0.45098039215686275, 6.272837960958401, 1.6819414150229712, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(730582, 'HP:0030312', 'Obliteration of the calvarial diploe', 'XPO:0140017', 'abnormally necrotic lateral nasal prominence', 0.40384615384615385, 4.5318002188002176, 1.3528303989641963, 'UPHENO:0087907', 'abnormal head morphology'),
(730583, 'HP:0030312', 'Obliteration of the calvarial diploe', 'XPO:0139715', 'abnormally necrotic head', 0.42, 4.5318002188002176, 1.3796217205799897, 'UPHENO:0087907', 'abnormal head morphology'),
(730584, 'HP:0030312', 'Obliteration of the calvarial diploe', 'XPO:0128582', 'decreased size of the head region', 0.40384615384615385, 4.5318002188002176, 1.3528303989641963, 'UPHENO:0087907', 'abnormal head morphology'),
(730585, 'HP:0030312', 'Obliteration of the calvarial diploe', 'XPO:0141829', 'increased width of head', 0.5081967213114754, 7.024697770424301, 1.8894254087244782, 'HP:0000929', 'Abnormal skull morphology'),
(730586, 'HP:0030312', 'Obliteration of the calvarial diploe', 'XPO:0102005', 'abnormal splanchnocranium morphology', 0.49056603773584906, 4.638757693672553, 1.508514826510376, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(730587, 'HP:0030312', 'Obliteration of the calvarial diploe', 'XPO:0142059', 'abnormal nasal region morphology', 0.45652173913043476, 4.5318002188002176, 1.4383550734357495, 'UPHENO:0087907', 'abnormal head morphology'),
(730588, 'HP:0030312', 'Obliteration of the calvarial diploe', 'XPO:0130880', 'increased size of the suspensorium', 0.43333333333333335, 4.638757693672553, 1.4177899470389728, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(730589, 'HP:0030312', 'Obliteration of the calvarial diploe', 'XPO:0103152', 'abnormal otic region morphology', 0.5740740740740741, 7.024697770424301, 2.008157580521644, 'HP:0000929', 'Abnormal skull morphology'),
(730590, 'HP:0030312', 'Obliteration of the calvarial diploe', 'XPO:0141723', 'abnormal posterior notochord morphology', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(730591, 'HP:0030312', 'Obliteration of the calvarial diploe', 'XPO:0103138', 'abnormal upper jaw morphology', 0.44285714285714284, 7.024697770424301, 1.7637850163909, 'HP:0000929', 'Abnormal skull morphology'),
(730592, 'HP:0030312', 'Obliteration of the calvarial diploe', 'XPO:0140510', 'abnormally necrotic postcranial axial skeleton', 0.40350877192982454, 6.272837960958401, 1.5909573036826314, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(730593, 'HP:0030312', 'Obliteration of the calvarial diploe', 'XPO:0100693', 'abnormal vertebral centrum', 0.4107142857142857, 6.272837960958401, 1.6050994245019483, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(730594, 'HP:0030312', 'Obliteration of the calvarial diploe', 'XPO:0130147', 'increased size of the fenestra basicranialis', 0.45614035087719296, 4.638757693672553, 1.4546217934659431, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(730595, 'HP:0030312', 'Obliteration of the calvarial diploe', 'XPO:0102806', 'abnormal articular system morphology', 0.43478260869565216, 4.638757693672553, 1.4201588541997616, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(730596, 'HP:0030312', 'Obliteration of the calvarial diploe', 'XPO:0100584', 'abnormal vertebral column', 0.46938775510204084, 6.272837960958401, 1.7159234623412336, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(730597, 'HP:0030312', 'Obliteration of the calvarial diploe', 'XPO:0100226', 'abnormal vertebral element', 0.41818181818181815, 6.272837960958401, 1.6196255072310737, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(730598, 'HP:0030312', 'Obliteration of the calvarial diploe', 'XPO:0130449', 'increased size of the fenestra subocularis', 0.45614035087719296, 4.638757693672553, 1.4546217934659431, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(730599, 'HP:0030312', 'Obliteration of the calvarial diploe', 'XPO:0101659', 'abnormal lower jaw morphology', 0.45588235294117646, 7.024697770424301, 1.78953506483714, 'HP:0000929', 'Abnormal skull morphology'),
(730600, 'HP:0030312', 'Obliteration of the calvarial diploe', 'XPO:0102734', 'abnormal craniofacial region morphology', 0.4375, 4.5318002188002176, 1.4080705222839853, 'UPHENO:0087907', 'abnormal head morphology'),
(730601, 'HP:0030312', 'Obliteration of the calvarial diploe', 'XPO:0129771', 'increased size of the dermatocranium', 0.4262295081967213, 4.638757693672553, 1.4061206955371255, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(730602, 'HP:0030312', 'Obliteration of the calvarial diploe', 'XPO:0140560', 'abnormally necrotic orbital region', 0.4696969696969697, 7.024697770424301, 1.8164468766813286, 'HP:0000929', 'Abnormal skull morphology'),
(730603, 'HP:0030312', 'Obliteration of the calvarial diploe', 'XPO:0129406', 'decreased size of the suspensorium', 0.43333333333333335, 4.638757693672553, 1.4177899470389728, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(730604, 'HP:0030312', 'Obliteration of the calvarial diploe', 'XPO:0141185', 'abnormally necrotic occipital region', 0.5344827586206896, 7.024697770424301, 1.9376738226061134, 'HP:0000929', 'Abnormal skull morphology'),
(730605, 'HP:0030312', 'Obliteration of the calvarial diploe', 'XPO:0140335', 'abnormally necrotic pharyngeal region', 0.44680851063829785, 4.5318002188002176, 1.422971154406314, 'UPHENO:0087907', 'abnormal head morphology'),
(730606, 'HP:0030312', 'Obliteration of the calvarial diploe', 'XPO:0103332', 'decreased size of the chondrocranium', 0.4262295081967213, 4.638757693672553, 1.4061206955371255, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(730607, 'HP:0030312', 'Obliteration of the calvarial diploe', 'XPO:0102665', 'abnormal suspensorium morphology', 0.49056603773584906, 4.638757693672553, 1.508514826510376, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(730608, 'HP:0030312', 'Obliteration of the calvarial diploe', 'XPO:0102572', 'abnormal hatching gland primordium morphology', 0.42, 4.5318002188002176, 1.3796217205799897, 'UPHENO:0087907', 'abnormal head morphology'),
(730609, 'HP:0030312', 'Obliteration of the calvarial diploe', 'XPO:0107372', 'abnormal flexural organ morphology', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(730610, 'HP:0030312', 'Obliteration of the calvarial diploe', 'XPO:0140223', 'abnormally necrotic head region', 0.42, 4.5318002188002176, 1.3796217205799897, 'UPHENO:0087907', 'abnormal head morphology'),
(730611, 'HP:0030312', 'Obliteration of the calvarial diploe', 'XPO:0140668', 'abnormally necrotic medial nasal prominence', 0.40384615384615385, 4.5318002188002176, 1.3528303989641963, 'UPHENO:0087907', 'abnormal head morphology'),
(730612, 'HP:0030312', 'Obliteration of the calvarial diploe', 'XPO:0140672', 'abnormally necrotic olfactory region', 0.5254237288135594, 7.024697770424301, 1.9211826816637279, 'HP:0000929', 'Abnormal skull morphology'),
(730613, 'HP:0030312', 'Obliteration of the calvarial diploe', 'XPO:0131600', 'decreased size of the intercanthal region', 0.40384615384615385, 4.5318002188002176, 1.3528303989641963, 'UPHENO:0087907', 'abnormal head morphology'),
(730614, 'HP:0030312', 'Obliteration of the calvarial diploe', 'XPO:0140639', 'abnormally necrotic upper jaw', 0.41333333333333333, 7.024697770424301, 1.7039782114536297, 'HP:0000929', 'Abnormal skull morphology'),
(730615, 'HP:0010763', 'Low insertion of columella', 'XPO:0103115', 'abnormal nostril morphology', 0.5370370370370371, 9.601025046317446, 2.2707060671501944, 'UPHENO:0021517', 'abnormal nose morphology'),
(730616, 'HP:0010763', 'Low insertion of columella', 'XPO:0115526', 'abnormally incomplete structure of head', 0.45652173913043476, 4.5318002188002176, 1.4383550734357495, 'UPHENO:0087907', 'abnormal head morphology'),
(730617, 'HP:0010763', 'Low insertion of columella', 'XPO:0141339', 'decreased pigmentation in the head', 0.4375, 4.5318002188002176, 1.4080705222839853, 'UPHENO:0087907', 'abnormal head morphology'),
(730618, 'HP:0010763', 'Low insertion of columella', 'XPO:0130324', 'increased size of the choana', 0.43283582089552236, 9.601025046317446, 2.038545451384708, 'UPHENO:0021517', 'abnormal nose morphology'),
(730619, 'HP:0010763', 'Low insertion of columella', 'XPO:0126871', 'abnormally localised choana', 0.5272727272727272, 9.601025046317446, 2.2499685910664535, 'UPHENO:0021517', 'abnormal nose morphology'),
(730620, 'HP:0010763', 'Low insertion of columella', 'XPO:0103739', 'increased size of the pharyngeal region', 0.42857142857142855, 4.5318002188002176, 1.3936283915633758, 'UPHENO:0087907', 'abnormal head morphology'),
(730621, 'HP:0010763', 'Low insertion of columella', 'XPO:0130062', 'increased size of the head region', 0.40384615384615385, 4.5318002188002176, 1.3528303989641963, 'UPHENO:0087907', 'abnormal head morphology'),
(730622, 'HP:0010763', 'Low insertion of columella', 'XPO:0101334', 'abnormal olfactory pit', 0.41304347826086957, 9.116652820832241, 1.9405086939288154, 'HP:0000366', 'Abnormality of the nose'),
(730623, 'HP:0010763', 'Low insertion of columella', 'XPO:0102572', 'abnormal hatching gland primordium morphology', 0.42, 4.5318002188002176, 1.3796217205799897, 'UPHENO:0087907', 'abnormal head morphology'),
(730624, 'HP:0010763', 'Low insertion of columella', 'XPO:0140335', 'abnormally necrotic pharyngeal region', 0.44680851063829785, 4.5318002188002176, 1.422971154406314, 'UPHENO:0087907', 'abnormal head morphology'),
(730625, 'HP:0010763', 'Low insertion of columella', 'XPO:0140914', 'abnormally necrotic intercanthal region', 0.42, 4.5318002188002176, 1.3796217205799897, 'UPHENO:0087907', 'abnormal head morphology'),
(730626, 'HP:0010763', 'Low insertion of columella', 'XPO:0127898', 'abnormally localised nostril', 0.5178571428571429, 9.601025046317446, 2.2297890929381237, 'UPHENO:0021517', 'abnormal nose morphology'),
(730627, 'HP:0010763', 'Low insertion of columella', 'XPO:0141839', 'edematous pharyngeal region', 0.45652173913043476, 4.5318002188002176, 1.4383550734357495, 'UPHENO:0087907', 'abnormal head morphology'),
(730628, 'HP:0010763', 'Low insertion of columella', 'XPO:0141835', 'edematous head', 0.44680851063829785, 4.5318002188002176, 1.422971154406314, 'UPHENO:0087907', 'abnormal head morphology'),
(730629, 'HP:0010763', 'Low insertion of columella', 'XPO:0128440', 'decreased size of the Jacobsons organ', 0.42857142857142855, 9.467216006125252, 2.01429349607732, 'UPHENO:0087950', 'abnormal nose morphology'),
(730630, 'HP:0010763', 'Low insertion of columella', 'XPO:0142059', 'abnormal nasal region morphology', 0.45652173913043476, 4.5318002188002176, 1.4383550734357495, 'UPHENO:0087907', 'abnormal head morphology'),
(730631, 'HP:0010763', 'Low insertion of columella', 'XPO:0102734', 'abnormal craniofacial region morphology', 0.4375, 4.5318002188002176, 1.4080705222839853, 'UPHENO:0087907', 'abnormal head morphology'),
(730632, 'HP:0010763', 'Low insertion of columella', 'XPO:0128599', 'decreased size of the olfactory pit', 0.46551724137931033, 9.467216006125252, 2.099321861629007, 'UPHENO:0087950', 'abnormal nose morphology'),
(730633, 'HP:0010763', 'Low insertion of columella', 'XPO:0102226', 'abnormal Jacobsons organ morphology', 0.4909090909090909, 9.467216006125252, 2.1558159483144523, 'UPHENO:0087950', 'abnormal nose morphology'),
(730634, 'HP:0010763', 'Low insertion of columella', 'XPO:0140593', 'abnormally necrotic Jacobsons organ', 0.45, 9.467216006125252, 2.0640366282496934, 'UPHENO:0087950', 'abnormal nose morphology'),
(730635, 'HP:0010763', 'Low insertion of columella', 'XPO:0129920', 'increased size of the Jacobsons organ', 0.43548387096774194, 9.467216006125252, 2.030472820215821, 'UPHENO:0087950', 'abnormal nose morphology'),
(730636, 'HP:0010763', 'Low insertion of columella', 'XPO:0103707', 'increased pigmentation in the head', 0.4375, 4.5318002188002176, 1.4080705222839853, 'UPHENO:0087907', 'abnormal head morphology'),
(730637, 'HP:0010763', 'Low insertion of columella', 'XPO:0102259', 'abnormal pharyngeal region morphology', 0.4772727272727273, 4.5318002188002176, 1.4706816956370683, 'UPHENO:0087907', 'abnormal head morphology'),
(730638, 'HP:0010763', 'Low insertion of columella', 'XPO:0102082', 'abnormal circumpharyngeal ridge morphology', 0.42857142857142855, 4.5318002188002176, 1.3936283915633758, 'UPHENO:0087907', 'abnormal head morphology'),
(730639, 'HP:0010763', 'Low insertion of columella', 'XPO:0131600', 'decreased size of the intercanthal region', 0.40384615384615385, 4.5318002188002176, 1.3528303989641963, 'UPHENO:0087907', 'abnormal head morphology'),
(730640, 'HP:0010763', 'Low insertion of columella', 'XPO:0130079', 'increased size of the olfactory pit', 0.46551724137931033, 9.467216006125252, 2.099321861629007, 'UPHENO:0087950', 'abnormal nose morphology'),
(730641, 'HP:0010763', 'Low insertion of columella', 'XPO:0140223', 'abnormally necrotic head region', 0.42, 4.5318002188002176, 1.3796217205799897, 'UPHENO:0087907', 'abnormal head morphology'),
(730642, 'HP:0010763', 'Low insertion of columella', 'XPO:0133429', 'abnormal cilium morphology in the olfactory pit', 0.4426229508196721, 9.467216006125252, 2.0470483835704494, 'UPHENO:0087950', 'abnormal nose morphology'),
(730643, 'HP:0010763', 'Low insertion of columella', 'XPO:0141298', 'abnormal intercanthal region morphology', 0.44680851063829785, 4.5318002188002176, 1.422971154406314, 'UPHENO:0087907', 'abnormal head morphology'),
(730644, 'HP:0010763', 'Low insertion of columella', 'XPO:0101634', 'abnormal head morphology', 0.4666666666666667, 4.5318002188002176, 1.4542489821577214, 'UPHENO:0087907', 'abnormal head morphology'),
(730645, 'HP:0010763', 'Low insertion of columella', 'XPO:0140668', 'abnormally necrotic medial nasal prominence', 0.40384615384615385, 4.5318002188002176, 1.3528303989641963, 'UPHENO:0087907', 'abnormal head morphology'),
(730646, 'HP:0010763', 'Low insertion of columella', 'XPO:0102804', 'abnormal pharyngeal pouch morphology', 0.4375, 4.5318002188002176, 1.4080705222839853, 'UPHENO:0087907', 'abnormal head morphology'),
(730647, 'HP:0010763', 'Low insertion of columella', 'XPO:0128582', 'decreased size of the head region', 0.40384615384615385, 4.5318002188002176, 1.3528303989641963, 'UPHENO:0087907', 'abnormal head morphology'),
(730648, 'HP:0010763', 'Low insertion of columella', 'XPO:0102538', 'abnormal lateral nasal prominence morphology', 0.4375, 4.5318002188002176, 1.4080705222839853, 'UPHENO:0087907', 'abnormal head morphology'),
(730649, 'HP:0010763', 'Low insertion of columella', 'XPO:0130934', 'increased size of the nostril', 0.4603174603174603, 9.601025046317446, 2.1022653176431305, 'UPHENO:0021517', 'abnormal nose morphology'),
(730650, 'HP:0010763', 'Low insertion of columella', 'XPO:0140017', 'abnormally necrotic lateral nasal prominence', 0.40384615384615385, 4.5318002188002176, 1.3528303989641963, 'UPHENO:0087907', 'abnormal head morphology'),
(730651, 'HP:0010763', 'Low insertion of columella', 'XPO:0101483', 'abnormal nostril', 0.6304347826086957, 9.601025046317446, 2.4602479830081725, 'UPHENO:0021517', 'abnormal nose morphology'),
(730652, 'HP:0010763', 'Low insertion of columella', 'XPO:0103358', 'decreased size of the pharyngeal region', 0.42857142857142855, 4.5318002188002176, 1.3936283915633758, 'UPHENO:0087907', 'abnormal head morphology'),
(730653, 'HP:0010763', 'Low insertion of columella', 'XPO:0102966', 'abnormal olfactory pit morphology', 0.5094339622641509, 9.467216006125252, 2.1961150611047175, 'UPHENO:0087950', 'abnormal nose morphology'),
(730654, 'HP:0010763', 'Low insertion of columella', 'XPO:0131638', 'increased size of the intercanthal region', 0.40384615384615385, 4.5318002188002176, 1.3528303989641963, 'UPHENO:0087907', 'abnormal head morphology'),
(730655, 'HP:0010763', 'Low insertion of columella', 'XPO:0128846', 'decreased size of the choana', 0.43283582089552236, 9.601025046317446, 2.038545451384708, 'UPHENO:0021517', 'abnormal nose morphology'),
(730656, 'HP:0010763', 'Low insertion of columella', 'XPO:0139715', 'abnormally necrotic head', 0.42, 4.5318002188002176, 1.3796217205799897, 'UPHENO:0087907', 'abnormal head morphology'),
(730657, 'HP:0010763', 'Low insertion of columella', 'XPO:0125246', 'absent choana', 0.48333333333333334, 9.601025046317446, 2.1541809206873577, 'UPHENO:0021517', 'abnormal nose morphology'),
(730658, 'HP:0010763', 'Low insertion of columella', 'XPO:0133370', 'olfactory pit fused with brain', 0.48214285714285715, 9.467216006125252, 2.1364808855643473, 'UPHENO:0087950', 'abnormal nose morphology'),
(730659, 'HP:0010763', 'Low insertion of columella', 'XPO:0103101', 'abnormal medial nasal prominence morphology', 0.4375, 4.5318002188002176, 1.4080705222839853, 'UPHENO:0087907', 'abnormal head morphology'),
(730660, 'HP:0010763', 'Low insertion of columella', 'XPO:0100594', 'abnormal Jacobsons organ', 0.40425531914893614, 9.116652820832241, 1.9197539935251045, 'HP:0000366', 'Abnormality of the nose'),
(730661, 'HP:0010763', 'Low insertion of columella', 'XPO:0129460', 'decreased size of the nostril', 0.453125, 9.601025046317446, 2.0857767076349742, 'UPHENO:0021517', 'abnormal nose morphology'),
(730662, 'HP:0010763', 'Low insertion of columella', 'XPO:0100420', 'abnormal choana', 0.6041666666666666, 9.601025046317446, 2.4084474872450072, 'UPHENO:0021517', 'abnormal nose morphology'),
(730663, 'HP:0010763', 'Low insertion of columella', 'XPO:0126234', 'absent nostril', 0.47540983606557374, 9.601025046317446, 2.136450735058322, 'UPHENO:0021517', 'abnormal nose morphology'),
(730664, 'HP:0010763', 'Low insertion of columella', 'XPO:0102052', 'abnormal choana morphology', 0.47540983606557374, 9.601025046317446, 2.136450735058322, 'UPHENO:0021517', 'abnormal nose morphology'),
(730665, 'HP:0001747', 'Accessory spleen', 'XPO:0141626', 'metaplastic spleen', 0.4603174603174603, 10.484129389061598, 2.1968222081025313, 'HP:0001743', 'Abnormality of the spleen'),
(730666, 'HP:0001747', 'Accessory spleen', 'XPO:0130675', 'increased size of the spleen', 0.4111111111111111, 11.212049843624797, 2.1469509237627555, 'UPHENO:0076790', 'abnormal spleen morphology'),
(730667, 'HP:0001747', 'Accessory spleen', 'XPO:0102078', 'abnormal spleen morphology', 0.5211267605633803, 11.212049843624797, 2.4172089719929772, 'UPHENO:0076790', 'abnormal spleen morphology'),
(730668, 'HP:0001747', 'Accessory spleen', 'XPO:0129199', 'decreased size of the spleen', 0.44047619047619047, 11.212049843624797, 2.222305335130395, 'UPHENO:0076790', 'abnormal spleen morphology'),
(730669, 'HP:0001747', 'Accessory spleen', 'XPO:0125198', 'absent spleen', 0.5, 11.212049843624797, 2.367704568102279, 'UPHENO:0076790', 'abnormal spleen morphology'),
(730670, 'HP:0001747', 'Accessory spleen', 'XPO:0100446', 'abnormal spleen', 0.47540983606557374, 10.484129389061598, 2.232545236751999, 'HP:0001743', 'Abnormality of the spleen'),
(730671, 'HP:0001747', 'Accessory spleen', 'XPO:0141656', 'neoplastic spleen', 0.5068493150684932, 11.212049843624797, 2.383866561650428, 'UPHENO:0076790', 'abnormal spleen morphology'),
(730672, 'HP:0001747', 'Accessory spleen', 'XPO:0140119', 'abnormally necrotic spleen', 0.4625, 11.212049843624797, 2.2771853356010507, 'UPHENO:0076790', 'abnormal spleen morphology'),
(730673, 'HP:0011049', 'Agenesis of primary maxillary lateral incisor', 'XPO:0129225', 'decreased size of the upper jaw', 0.44144144144144143, 8.81758714901448, 1.9729288839429773, 'UPHENO:0087585', 'abnormal midface morphology'),
(730674, 'HP:0011049', 'Agenesis of primary maxillary lateral incisor', 'XPO:0101659', 'abnormal lower jaw morphology', 0.4519230769230769, 8.608423498638606, 1.9723958109268225, 'UPHENO:0088116', 'abnormal jaw skeleton morphology'),
(730675, 'HP:0011049', 'Agenesis of primary maxillary lateral incisor', 'XPO:0128880', 'decreased size of the lower jaw', 0.42342342342342343, 8.608423498638606, 1.9091904431125257, 'UPHENO:0088116', 'abnormal jaw skeleton morphology'),
(730676, 'HP:0011049', 'Agenesis of primary maxillary lateral incisor', 'XPO:0140897', 'abnormally necrotic lower jaw', 0.43119266055045874, 8.608423498638606, 1.9266263341714887, 'UPHENO:0088116', 'abnormal jaw skeleton morphology'),
(730677, 'HP:0011049', 'Agenesis of primary maxillary lateral incisor', 'XPO:0130358', 'increased size of the lower jaw', 0.42342342342342343, 8.608423498638606, 1.9091904431125257, 'UPHENO:0088116', 'abnormal jaw skeleton morphology'),
(730678, 'HP:0011049', 'Agenesis of primary maxillary lateral incisor', 'XPO:0103138', 'abnormal upper jaw morphology', 0.47115384615384615, 8.81758714901448, 2.0382443668645083, 'UPHENO:0087585', 'abnormal midface morphology'),
(730679, 'HP:0011049', 'Agenesis of primary maxillary lateral incisor', 'XPO:0130701', 'increased size of the upper jaw', 0.44144144144144143, 8.81758714901448, 1.9729288839429773, 'UPHENO:0087585', 'abnormal midface morphology'),
(730680, 'HP:0011049', 'Agenesis of primary maxillary lateral incisor', 'XPO:0101816', 'abnormal tooth morphology', 0.4017857142857143, 9.872199840740173, 1.9916096165120074, 'HP:0006482', 'Abnormal dental morphology'),
(730681, 'HP:0011049', 'Agenesis of primary maxillary lateral incisor', 'XPO:0140639', 'abnormally necrotic upper jaw', 0.44954128440366975, 8.81758714901448, 1.990946873301561, 'UPHENO:0087585', 'abnormal midface morphology'),
(730682, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0141809', 'abnormal catalytic activity', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(730683, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0100546', 'abnormal whole organism', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(730684, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0100852', 'abnormal interdigital region', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(730685, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0100422', 'abnormal notochord', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(730686, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0100665', 'abnormal egg jelly', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(730687, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0101157', 'abnormal female organism', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(730688, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0100638', 'abnormal polar body', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(730689, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0100802', 'abnormal exocrine cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(730690, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0100643', 'abnormal thoracic region', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(730691, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0100890', 'abnormal pharyngeal cavity', 0.44, 4.96264005835567, 1.4776879324392194, 'HP:0002664', 'Neoplasm'),
(730692, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0131677', 'abnormal actin filament', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(730693, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0100372', 'abnormal hematological system', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(730694, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0141796', 'abnormal demethylation', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(730695, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0141775', 'abnormal nitrogen compound metabolic process', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(730696, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0131469', 'abnormal heart process', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(730697, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0116433', 'abnormal axis specification', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(730698, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0131745', 'abnormal axis elongation', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(730699, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0107271', 'abnormal apical region', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(730700, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0101302', 'abnormal subcortical cytoplasm', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(730701, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0115391', 'abnormally undifferentiated alimentary system', 0.4583333333333333, 4.96264005835567, 1.508158930643479, 'HP:0002664', 'Neoplasm'),
(730702, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0100587', 'abnormal vestibuloauditory system', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(730703, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0100545', 'abnormal male organism', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(730704, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0131740', 'abnormal detection of nodal flow', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(730705, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0101283', 'abnormal left-ventral blastomere', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(730706, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0100225', 'abnormal endocrine system', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(730707, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0141778', 'abnormal biosynthetic process', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(730708, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0100691', 'abnormal keratin accumulating cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(730709, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0141911', 'abnormal ribose phosphate metabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(730710, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0100377', 'abnormal connective tissue', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(730711, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0100551', 'abnormal oocyte cortex', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(730712, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0101311', 'abnormal bottle cell', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(730713, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0100862', 'abnormal blastomere V1', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(730714, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0131703', 'abnormal cell division', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(730715, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0115512', 'abnormally semi-erect whole organism', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(730716, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0141787', 'abnormal hormone metabolic process', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(730717, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0100585', 'abnormal elastica externa', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(730718, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0128000', 'absent behavior', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(730719, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0101021', 'abnormal dorsal foregut', 0.4074074074074074, 4.96264005835567, 1.421905875953408, 'HP:0002664', 'Neoplasm'),
(730720, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0131687', 'abnormal astral microtubule', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(730721, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0100032', 'abnormal nervous system', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(730722, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0100976', 'abnormal multiciliated cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(730723, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0133401', 'absent determination of left/right symmetry in lateral plate mesoderm', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(730724, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0141266', 'abnormal surface breathing', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(730725, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0100969', 'abnormal disaggregated/reaggregated ectoderm treated with activin', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(730726, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0101241', 'abnormal nucleate erythrocyte', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(730727, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0115509', 'abnormally semi-viable whole organism', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(730728, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0141794', 'abnormal prosthetic group metabolic process', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(730729, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0100277', 'abnormal blastocoel', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(730730, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0131723', 'abnormal pathway-restricted SMAD protein phosphorylation', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(730731, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0101535', 'abnormal absorptive cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(730732, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0101221', 'abnormal larval immune system', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(730733, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0100062', 'abnormal anatomical space', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(730734, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0100547', 'abnormal blastomere V2', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(730735, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0101264', 'abnormal mitotic spindle', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(730736, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0141772', 'abnormal water homeostasis', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(730737, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0100437', 'abnormal proepicardium', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(730738, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0100486', 'abnormal oral evagination', 0.4230769230769231, 4.96264005835567, 1.4489922312515684, 'HP:0002664', 'Neoplasm'),
(730739, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0141860', 'abnormal malate-aspartate shuttle', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(730740, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0101472', 'abnormal zygote cortex', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(730741, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0101448', 'abnormal myelin accumulating cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(730742, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0101411', 'abnormal marginal zone (sensu neural)', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(730743, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0100307', 'abnormal blastomere', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(730744, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0100010', 'abnormal multicellular anatomical structure', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(730745, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0100917', 'abnormal stage III oocyte', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(730746, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0141892', 'abnormal inositol metabolic process', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(730747, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0131675', 'abnormal spindle microtubule', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(730748, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0100533', 'abnormal melanoblast', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(730749, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0101480', 'abnormal stage V oocyte', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(730750, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0107259', 'abnormal animal-vegetal axis', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(730751, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0107258', 'abnormal anatomical axis', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(730752, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0100258', 'abnormal organ part', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(730753, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0100014', 'abnormal tissue', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(730754, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0100481', 'abnormal anatomical line', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(730755, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0100429', 'abnormal spermatid', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(730756, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0100493', 'abnormal liver and biliary system', 0.4583333333333333, 4.96264005835567, 1.508158930643479, 'HP:0002664', 'Neoplasm'),
(730757, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0101071', 'abnormal endoplasmic reticulum', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(730758, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0116429', 'abnormal behavior', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(730759, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0100688', 'abnormal adipose tissue', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(730760, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0141960', 'absent cilium motility in brain', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(730761, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0100386', 'abnormal limb', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(730762, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0100894', 'abnormal nucleus', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(730763, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0100218', 'abnormal epithelial cell', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(730764, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0100084', 'abnormal anatomical group', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(730765, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0141784', 'abnormal cellular hormone metabolic process', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(730766, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0100573', 'abnormal extraembryonic structure', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(730767, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0107263', 'abnormal anatomical side', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(730768, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0100104', 'abnormal embryonic structure', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(730769, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0100899', 'abnormal secondary spermatogonium', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(730770, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0100842', 'abnormal left-dorsal blastomere', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
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(730773, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0101377', 'abnormal manicotto glandulare', 0.4230769230769231, 4.96264005835567, 1.4489922312515684, 'HP:0002664', 'Neoplasm'),
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(730775, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0133403', 'abnormal developmental process', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(730776, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0141792', 'abnormal small molecule metabolic process', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
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(730778, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0101409', 'abnormal perivitelline space', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(730779, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0131666', 'abnormal adherens junction', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(730780, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0107253', 'abnormal enteric nervous system', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(730781, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0100273', 'abnormal visual system', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(730782, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0100791', 'abnormal multiciliated cell precursor', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
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(730784, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0100503', 'abnormal blastomere D2', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(730785, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0107278', 'abnormal medial region', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(730786, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0100152', 'abnormal alimentary system', 0.4782608695652174, 4.96264005835567, 1.5405961669588706, 'HP:0002664', 'Neoplasm'),
(730787, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0101220', 'abnormal centriole', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(730788, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0100003', 'abnormal organism subdivision', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(730789, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0131691', 'abnormal molecular function', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(730790, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0101461', 'abnormal sperm entry point', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(730791, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0131729', 'abnormal regulation of growth rate', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(730792, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0131744', 'abnormal apical constriction', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(730793, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0100754', 'abnormal electrically active cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(730794, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0100239', 'abnormal acellular anatomical structure', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(730795, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0101113', 'abnormal stage IV oocyte', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(730796, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0101061', 'abnormal plasma membrane', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(730797, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0141724', 'abnormal prevention of polyspermy', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(730798, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0141754', 'abnormal homeostatic process', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(730799, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0141798', 'abnormal lipid metabolic process', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(730800, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0101132', 'abnormal apoptotic cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(730801, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0100028', 'abnormal anatomical cluster', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(730802, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0101378', 'abnormal blastomere D1', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(730803, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0107261', 'abnormal dorsal-ventral axis', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(730804, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0100289', 'abnormal chondroblast', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(730805, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0101110', 'abnormal cell-free extract', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(730806, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0100070', 'abnormal anatomical system', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(730807, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0101463', 'abnormal right-ventral blastomere', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(730808, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0131725', 'abnormal phosphorylation of RNA polymerase II C-terminal domain', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(730809, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0100674', 'abnormal secondary oogonium', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(730810, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0100031', 'abnormal central nervous system', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(730811, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0141781', 'abnormal secondary metabolic process', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(730812, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0141271', 'increased surface breathing', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(730813, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0141907', 'abnormal putrescine metabolic process', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(730814, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0100308', 'abnormal early embryonic cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(730815, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0101570', 'abnormal forelimb region', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(730816, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0100704', 'abnormal Merkel cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(730817, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0101497', 'abnormal ciliary axoneme', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(730818, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0100081', 'abnormal anatomical entity in vitro', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(730819, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0101547', 'abnormal lampbrush chromosome', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(730820, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0100295', 'abnormal extracellular matrix', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(730821, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0107312', 'abnormal filopodium', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(730822, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0100427', 'abnormal olfactory system', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(730823, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0141770', 'abnormal urate homeostasis', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(730824, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0100956', 'abnormal centrosome', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(730825, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0100902', 'abnormal spermatocyte', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(730826, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0100888', 'abnormal microtubule', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(730827, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0100515', 'abnormal somatic stem cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(730828, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0100423', 'abnormal process', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(730829, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0107273', 'abnormal basal region', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(730830, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0100724', 'abnormal kinetochore', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(730831, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0100728', 'abnormal cell condensation', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(730832, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0141265', 'abnormal escape behavior', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(730833, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0131685', 'abnormal cortical actin cytoskeleton', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(730834, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0100887', 'abnormal right-dorsal blastomere', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(730835, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0141276', 'decreased surface breathing', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(730836, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0101467', 'abnormal alkali secreting cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(730837, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0101569', 'abnormal activin-induced ectoderm', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(730838, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0131730', 'abnormal regulation of protein folding', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(730839, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0141783', 'abnormal collagen metabolic process', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(730840, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0100574', 'abnormal gastrula cell', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(730841, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0141748', 'abnormal gas homeostasis', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(730842, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0101451', 'abnormal dorsal lymph space', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(730843, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0100009', 'abnormal multi-tissue structure', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(730844, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0100344', 'abnormal portion of organism substance', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(730845, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0100205', 'abnormal limb segment', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(730846, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0100176', 'abnormal stage VI oocyte', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(730847, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0107272', 'abnormal axial region', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(730848, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0141745', 'abnormal creatinine homeostasis', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(730849, 'HP:0034557', 'Rhabdoid tumor', 'XPO:00000000', 'Xenopus phenotype', 0.5714285714285714, 1.4755025719078136, 0.918228907628411, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(730850, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0100989', 'abnormal right blastomere', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(730851, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0100274', 'abnormal sensory system', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(730852, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0100465', 'abnormal skeletal system', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(730853, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0116434', 'abnormal biological process', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(730854, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0131669', 'abnormal Roux spot', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(730855, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0100477', 'abnormal pericyte', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(730856, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0107260', 'abnormal anterior-posterior axis', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(730857, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0100004', 'abnormal cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(730858, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0100392', 'abnormal cilium', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(730859, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0141272', 'absent surface breathing', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(730860, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0141743', 'abnormal chemical homeostasis within a tissue', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(730861, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0100907', 'abnormal cytoplasm', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(730862, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0141904', 'abnormal glucosamine metabolic process', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(730863, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0101366', 'abnormal morula cell', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(730864, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0101435', 'abnormal paracrine cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(730865, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0101297', 'abnormal barrier cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(730866, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0100026', 'abnormal germ cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(730867, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0141600', 'absent metamorphosis', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(730868, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0141898', 'abnormal maltose metabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(730869, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0115505', 'dead whole organism', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(730870, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0101072', 'abnormal mitochondrial cloud', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(730871, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0141263', 'abnormal visually guided collision avoidance behavior', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(730872, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0101498', 'abnormal stage II oocyte', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(730873, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0100599', 'abnormal adult immune system', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(730874, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0100735', 'abnormal hindgut', 0.4230769230769231, 4.96264005835567, 1.4489922312515684, 'HP:0002664', 'Neoplasm'),
(730875, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0133388', 'absent insulin receptor signaling pathway', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(730876, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0131694', 'abnormal RNA polymerase II activity', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(730877, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0101347', 'abnormal hindlimb region', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(730878, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0141797', 'abnormal hydrogen metabolic process', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(730879, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0100581', 'abnormal immune system', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(730880, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0141315', 'abnormal anatomical region', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(730881, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0100172', 'abnormal stem cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(730882, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0101326', 'abnormal cementoblast', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(730883, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0141962', 'absent cilium motility in pronephric kidney', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(730884, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0131667', 'abnormal actin cytoskeleton', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(730885, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0101141', 'abnormal Keller explant', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(730886, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0141964', 'absent cilium motility in olfactory pit', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(730887, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0101513', 'abnormal basal body', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(730888, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0115508', 'abnormally peramorphic growth of whole organism', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(730889, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0141975', 'abnormal cilium motility', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(730890, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0141499', 'abnormal tadpole', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(730891, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0100784', 'abnormal left blastomere', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(730892, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0100626', 'abnormal primordial germ cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(730893, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0100337', 'abnormal zygote', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(730894, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0101381', 'abnormal ventral foregut', 0.4074074074074074, 4.96264005835567, 1.421905875953408, 'HP:0002664', 'Neoplasm'),
(730895, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0100762', 'abnormal intersomitic region', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(730896, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0100232', 'abnormal lymphatic system', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(730897, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0107262', 'abnormal left-right axis', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(730898, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0141777', 'abnormal catabolic process', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(730899, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0100823', 'abnormal blood', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(730900, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0107284', 'abnormal migrating myoblast', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(730901, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0131722', 'abnormal determination of left/right symmetry', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(730902, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0100156', 'abnormal foregut', 0.4230769230769231, 4.96264005835567, 1.4489922312515684, 'HP:0002664', 'Neoplasm'),
(730903, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0142054', 'abnormal digestive tract', 0.44, 4.96264005835567, 1.4776879324392194, 'HP:0002664', 'Neoplasm'),
(730904, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0141782', 'abnormal methylation', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(730905, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0141958', 'absent cilium motility in left-right organizer', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(730906, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0100108', 'abnormal cell part', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(730907, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0133340', 'abnormal cell adhesion', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(730908, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0141795', 'abnormal glycosylation', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(730909, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0100501', 'abnormal urogenital system', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(730910, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0101575', 'abnormal vitelline membrane', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(730911, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0131719', 'abnormal activation of meiosis', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(730912, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0100653', 'abnormal myoblast', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(730913, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0141959', 'absent cilium motility in floor plate', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(730914, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0101004', 'abnormal acid secreting cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(730915, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0100462', 'abnormal anterior foregut', 0.4074074074074074, 4.96264005835567, 1.421905875953408, 'HP:0002664', 'Neoplasm'),
(730916, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0101405', 'abnormal ring structure', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(730917, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0100715', 'abnormal ciliated cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(730918, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0142057', 'abnormal desmosome', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(730919, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0101228', 'abnormal mesenchymal stem cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(730920, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0100642', 'abnormal gustatory system', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(730921, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0141776', 'abnormal metabolic process', 0.5263157894736842, 1.8210412618256888, 0.9790009036675816, 'HP:0000118', 'Phenotypic abnormality'),
(730922, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0101101', 'abnormal posterior foregut', 0.4074074074074074, 4.96264005835567, 1.421905875953408, 'HP:0002664', 'Neoplasm'),
(730923, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0101389', 'abnormal wedge region', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(730924, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0101237', 'abnormal mucus secreting cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(730925, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0107339', 'abnormal yolk platelet', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(730926, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0141790', 'abnormal cellular metabolic process', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(730927, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0101136', 'abnormal ooplasm', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(730928, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0101240', 'abnormal ciliated non-epidermal cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(730929, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0101468', 'abnormal stage I oocyte', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(730930, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0141267', 'abnormal resting posture', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(730931, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0141786', 'abnormal pigment metabolic process', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(730932, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0100006', 'abnormal anatomical structure', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(730933, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0141877', 'abnormal 2-deoxyribose 1-phosphate metabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(730934, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0100417', 'abnormal dense regular connective tissue', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(730935, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0100721', 'abnormal centromere', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(730936, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0116494', 'absent biological process', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(730937, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0100025', 'abnormal oocyte', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(730938, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0100549', 'abnormal mitotic cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(730939, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0107288', 'abnormal larval alimentary system', 0.4583333333333333, 4.96264005835567, 1.508158930643479, 'HP:0002664', 'Neoplasm'),
(730940, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0141738', 'abnormal carbon dioxide homeostasis', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(730941, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0100317', 'abnormal respiratory system', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(730942, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0107276', 'abnormal dorsal region', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(730943, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0100285', 'abnormal progenitor cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(730944, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0100202', 'abnormal embryo', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(730945, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0101373', 'abnormal oxygen accumulating cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(730946, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0141771', 'abnormal urea homeostasis', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(730947, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0101109', 'abnormal egg cell-free extract', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(730948, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0101333', 'abnormal barrier epithelial cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(730949, 'HP:0034557', 'Rhabdoid tumor', 'XPO:0107270', 'abnormal proximal-distal axis', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(730950, 'HP:0500133', 'Hypotyrosinemia', 'XPO:0141853', 'abnormal glutamate metabolic process', 0.5189873417721519, 10.156767408123608, 2.295916748956743, 'UPHENO:0050249', 'abnormal alpha-amino acid metabolic process'),
(730951, 'HP:0500133', 'Hypotyrosinemia', 'XPO:0141913', 'abnormal L-serine metabolic process', 0.5256410256410257, 10.156767408123608, 2.310587292790176, 'UPHENO:0050249', 'abnormal alpha-amino acid metabolic process'),
(730952, 'HP:0500133', 'Hypotyrosinemia', 'XPO:0141896', 'abnormal lysine metabolic process', 0.5324675324675324, 10.156767408123608, 2.3255427064774006, 'UPHENO:0050249', 'abnormal alpha-amino acid metabolic process'),
(730953, 'HP:0500133', 'Hypotyrosinemia', 'XPO:0141918', 'abnormal tyrosine metabolic process', 0.5733333333333334, 14.30515924801628, 2.8638478722741776, 'UPHENO:0051525', 'abnormal tyrosine metabolic process'),
(730954, 'HP:0500133', 'Hypotyrosinemia', 'XPO:0141843', 'abnormal alanine metabolic process', 0.5394736842105263, 10.156767408123608, 2.3407923302441507, 'UPHENO:0050249', 'abnormal alpha-amino acid metabolic process'),
(730955, 'HP:0500133', 'Hypotyrosinemia', 'XPO:0141847', 'abnormal arginine metabolic process', 0.5324675324675324, 10.156767408123608, 2.3255427064774006, 'UPHENO:0050249', 'abnormal alpha-amino acid metabolic process'),
(730956, 'HP:0500133', 'Hypotyrosinemia', 'XPO:0141893', 'abnormal isoleucine metabolic process', 0.5324675324675324, 10.156767408123608, 2.3255427064774006, 'UPHENO:0050249', 'abnormal alpha-amino acid metabolic process'),
(730957, 'HP:0500133', 'Hypotyrosinemia', 'XPO:0141917', 'abnormal tryptophan metabolic process', 0.5526315789473685, 12.568193653850074, 2.6354469646425183, 'UPHENO:0050390', 'abnormal aromatic amino acid metabolic process'),
(730958, 'HP:0500133', 'Hypotyrosinemia', 'XPO:0141922', 'abnormal valine metabolic process', 0.5324675324675324, 10.156767408123608, 2.3255427064774006, 'UPHENO:0050249', 'abnormal alpha-amino acid metabolic process'),
(730959, 'HP:0500133', 'Hypotyrosinemia', 'XPO:0141868', 'abnormal asparagine metabolic process', 0.5324675324675324, 10.156767408123608, 2.3255427064774006, 'UPHENO:0050249', 'abnormal alpha-amino acid metabolic process'),
(730960, 'HP:0500133', 'Hypotyrosinemia', 'XPO:0141869', 'abnormal alpha-amino acid metabolic process', 0.5540540540540541, 10.156767408123608, 2.372213767465945, 'UPHENO:0050249', 'abnormal alpha-amino acid metabolic process'),
(730961, 'HP:0500133', 'Hypotyrosinemia', 'XPO:0141882', 'abnormal gamma-aminobutyric acid metabolic process', 0.5263157894736842, 10.007478699375595, 2.2950150440254076, 'UPHENO:0051195', 'abnormal amino acid metabolic process'),
(730962, 'HP:0500133', 'Hypotyrosinemia', 'XPO:0141889', 'abnormal homoserine metabolic process', 0.5256410256410257, 10.156767408123608, 2.310587292790176, 'UPHENO:0050249', 'abnormal alpha-amino acid metabolic process'),
(730963, 'HP:0500133', 'Hypotyrosinemia', 'XPO:0141912', 'abnormal D-serine metabolic process', 0.5256410256410257, 10.156767408123608, 2.310587292790176, 'UPHENO:0050249', 'abnormal alpha-amino acid metabolic process'),
(730964, 'HP:0500133', 'Hypotyrosinemia', 'XPO:0141905', 'abnormal ornithine metabolic process', 0.5394736842105263, 10.156767408123608, 2.3407923302441507, 'UPHENO:0050249', 'abnormal alpha-amino acid metabolic process'),
(730965, 'HP:0500133', 'Hypotyrosinemia', 'XPO:0141887', 'abnormal histidine metabolic process', 0.5526315789473685, 12.568193653850074, 2.6354469646425183, 'UPHENO:0050390', 'abnormal aromatic amino acid metabolic process'),
(730966, 'HP:0500133', 'Hypotyrosinemia', 'XPO:0141888', 'abnormal threonine metabolic process', 0.5324675324675324, 10.156767408123608, 2.3255427064774006, 'UPHENO:0050249', 'abnormal alpha-amino acid metabolic process'),
(730967, 'HP:0500133', 'Hypotyrosinemia', 'XPO:0141858', 'abnormal serine family amino acid metabolic process', 0.5394736842105263, 10.156767408123608, 2.3407923302441507, 'UPHENO:0050249', 'abnormal alpha-amino acid metabolic process'),
(730968, 'HP:0500133', 'Hypotyrosinemia', 'XPO:0141857', 'abnormal glycine metabolic process', 0.5256410256410257, 10.156767408123608, 2.310587292790176, 'UPHENO:0050249', 'abnormal alpha-amino acid metabolic process'),
(730969, 'HP:0500133', 'Hypotyrosinemia', 'XPO:0141848', 'abnormal proline metabolic process', 0.5324675324675324, 10.156767408123608, 2.3255427064774006, 'UPHENO:0050249', 'abnormal alpha-amino acid metabolic process'),
(730970, 'HP:0500133', 'Hypotyrosinemia', 'XPO:0141873', 'abnormal tricarboxylic acid metabolic process', 0.4605263157894737, 9.119292702704945, 2.049310681908075, 'HP:0004354', 'Abnormal circulating carboxylic acid concentration'),
(730971, 'HP:0500133', 'Hypotyrosinemia', 'XPO:0141895', 'abnormal leucine metabolic process', 0.5324675324675324, 10.156767408123608, 2.3255427064774006, 'UPHENO:0050249', 'abnormal alpha-amino acid metabolic process'),
(730972, 'HP:0010197', 'Curved middle toe phalanx', 'XPO:0102566', 'abnormal claw primordium morphology', 0.41346153846153844, 7.639349617137506, 1.7772386574535335, 'HP:0001780', 'Abnormal toe morphology'),
(730973, 'HP:0010197', 'Curved middle toe phalanx', 'XPO:0102180', 'abnormal hindlimb digit 3 morphology', 0.40186915887850466, 7.639349617137506, 1.752146970153439, 'HP:0001780', 'Abnormal toe morphology'),
(730974, 'HP:0010197', 'Curved middle toe phalanx', 'XPO:0101872', 'abnormal hindlimb digit 1 morphology', 0.40186915887850466, 7.639349617137506, 1.752146970153439, 'HP:0001780', 'Abnormal toe morphology'),
(730975, 'HP:0010197', 'Curved middle toe phalanx', 'XPO:0102876', 'abnormal hindlimb digit 4 morphology', 0.40186915887850466, 7.639349617137506, 1.752146970153439, 'UPHENO:0088132', 'abnormal pedal digit morphology'),
(730976, 'HP:0010197', 'Curved middle toe phalanx', 'XPO:0101809', 'abnormal hindlimb digit morphology', 0.4095238095238095, 7.639349617137506, 1.7687553696015759, 'HP:0001780', 'Abnormal toe morphology'),
(730977, 'HP:0010197', 'Curved middle toe phalanx', 'XPO:0102051', 'abnormal hindlimb digit 2 morphology', 0.40186915887850466, 7.639349617137506, 1.752146970153439, 'HP:0001780', 'Abnormal toe morphology'),
(730978, 'HP:0010197', 'Curved middle toe phalanx', 'XPO:0102948', 'abnormal hindlimb digit 5 morphology', 0.40186915887850466, 7.639349617137506, 1.752146970153439, 'HP:0001780', 'Abnormal toe morphology'),
(730979, 'HP:0008223', 'Compensated hypothyroidism', 'XPO:0100840', 'abnormal thyroid', 0.40540540540540543, 10.665155383737162, 2.0793536596874533, 'UPHENO:0002689', 'abnormal thyroid gland'),
(730980, 'HP:0008223', 'Compensated hypothyroidism', 'XPO:0141629', 'metaplastic thyroid', 0.41025641025641024, 10.665155383737162, 2.0917572427408575, 'UPHENO:0002689', 'abnormal thyroid gland'),
(730981, 'HP:0001580', 'Pigmented micronodular adrenocortical disease', 'XPO:0130297', 'increased size of the adrenal gland', 0.45614035087719296, 11.7363164126584, 2.313743176429865, 'UPHENO:0020671', 'abnormal adrenal gland morphology'),
(730982, 'HP:0001580', 'Pigmented micronodular adrenocortical disease', 'XPO:0129735', 'increased size of the endocrine system', 0.41304347826086957, 7.428233084304616, 1.7516230275015356, 'UPHENO:0076812', 'abnormal endocrine system morphology'),
(730983, 'HP:0001580', 'Pigmented micronodular adrenocortical disease', 'XPO:0125656', 'absent adrenal gland', 0.4482758620689655, 11.7363164126584, 2.293710390916559, 'UPHENO:0020671', 'abnormal adrenal gland morphology'),
(730984, 'HP:0001580', 'Pigmented micronodular adrenocortical disease', 'XPO:0127939', 'abnormally localised adrenal cortex', 0.5490196078431373, 12.819732420846037, 2.652976529550694, 'HP:0000849', 'Adrenocortical abnormality'),
(730985, 'HP:0001580', 'Pigmented micronodular adrenocortical disease', 'XPO:0102388', 'abnormal adrenal medulla morphology', 0.48, 11.30515924801628, 2.329479864486451, 'UPHENO:0087384', 'abnormal adrenal gland morphology'),
(730986, 'HP:0001580', 'Pigmented micronodular adrenocortical disease', 'XPO:0101976', 'abnormal portion of organism substance morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(730987, 'HP:0001580', 'Pigmented micronodular adrenocortical disease', 'XPO:0141659', 'neoplastic thyroid', 0.42, 7.767034997756375, 1.8061435986813665, 'UPHENO:0087376', 'abnormal endocrine gland morphology'),
(730988, 'HP:0001580', 'Pigmented micronodular adrenocortical disease', 'XPO:0103193', 'abnormal adrenal cortex morphology', 0.5957446808510638, 12.819732420846037, 2.7635642564726006, 'HP:0000849', 'Adrenocortical abnormality'),
(730989, 'HP:0001580', 'Pigmented micronodular adrenocortical disease', 'XPO:0101821', 'abnormal enteroendocrine cell morphology', 0.41304347826086957, 7.428233084304616, 1.7516230275015356, 'UPHENO:0076812', 'abnormal endocrine system morphology'),
(730990, 'HP:0001580', 'Pigmented micronodular adrenocortical disease', 'XPO:0101713', 'abnormal anatomical entity in vitro morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(730991, 'HP:0001580', 'Pigmented micronodular adrenocortical disease', 'XPO:0140682', 'abnormally necrotic adrenal gland', 0.49056603773584906, 11.7363164126584, 2.3994662406818823, 'UPHENO:0020671', 'abnormal adrenal gland morphology'),
(730992, 'HP:0001580', 'Pigmented micronodular adrenocortical disease', 'XPO:0102722', 'abnormal adrenal gland morphology', 0.5652173913043478, 11.7363164126584, 2.575571809576503, 'UPHENO:0020671', 'abnormal adrenal gland morphology'),
(730993, 'HP:0001580', 'Pigmented micronodular adrenocortical disease', 'XPO:0129934', 'increased size of the adrenal cortex', 0.5185185185185185, 12.819732420846037, 2.5782297536606213, 'HP:0000849', 'Adrenocortical abnormality'),
(730994, 'HP:0001580', 'Pigmented micronodular adrenocortical disease', 'XPO:0101561', 'abnormal adrenal cortex', 0.6666666666666666, 12.819732420846037, 2.9234377504171394, 'HP:0000849', 'Adrenocortical abnormality'),
(730995, 'HP:0001580', 'Pigmented micronodular adrenocortical disease', 'XPO:0102655', 'abnormal ultimobranchial body morphology', 0.4883720930232558, 7.767034997756375, 1.9476147304944988, 'UPHENO:0087376', 'abnormal endocrine gland morphology'),
(730996, 'HP:0001580', 'Pigmented micronodular adrenocortical disease', 'XPO:0128253', 'decreased size of the ultimobranchial body', 0.42, 7.767034997756375, 1.8061435986813665, 'UPHENO:0087376', 'abnormal endocrine gland morphology'),
(730997, 'HP:0001580', 'Pigmented micronodular adrenocortical disease', 'XPO:0129733', 'increased size of the ultimobranchial body', 0.42, 7.767034997756375, 1.8061435986813665, 'UPHENO:0087376', 'abnormal endocrine gland morphology'),
(730998, 'HP:0001580', 'Pigmented micronodular adrenocortical disease', 'XPO:0139937', 'abnormally necrotic ultimobranchial body', 0.4375, 7.767034997756375, 1.8433875912347935, 'UPHENO:0087376', 'abnormal endocrine gland morphology'),
(730999, 'HP:0001580', 'Pigmented micronodular adrenocortical disease', 'XPO:0129076', 'decreased size of the adrenal medulla', 0.4067796610169492, 11.30515924801628, 2.144460036151453, 'UPHENO:0087384', 'abnormal adrenal gland morphology'),
(731000, 'HP:0001580', 'Pigmented micronodular adrenocortical disease', 'XPO:0101835', 'abnormal endocrine cell morphology', 0.4318181818181818, 7.428233084304616, 1.7909902580935733, 'UPHENO:0076812', 'abnormal endocrine system morphology'),
(731001, 'HP:0001580', 'Pigmented micronodular adrenocortical disease', 'XPO:0102113', 'abnormal anatomical line morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(731002, 'HP:0001580', 'Pigmented micronodular adrenocortical disease', 'XPO:0101857', 'abnormal endocrine system morphology', 0.48717948717948717, 7.428233084304616, 1.9023361387150335, 'UPHENO:0076812', 'abnormal endocrine system morphology'),
(731003, 'HP:0001580', 'Pigmented micronodular adrenocortical disease', 'XPO:0102504', 'abnormal neuroendocrine cell morphology', 0.41304347826086957, 7.428233084304616, 1.7516230275015356, 'UPHENO:0076812', 'abnormal endocrine system morphology'),
(731004, 'HP:0001580', 'Pigmented micronodular adrenocortical disease', 'XPO:0128255', 'decreased size of the endocrine system', 0.41304347826086957, 7.428233084304616, 1.7516230275015356, 'UPHENO:0076812', 'abnormal endocrine system morphology'),
(731005, 'HP:0001580', 'Pigmented micronodular adrenocortical disease', 'XPO:0140590', 'abnormally necrotic adrenal medulla', 0.42105263157894735, 11.30515924801628, 2.181757789443257, 'UPHENO:0087384', 'abnormal adrenal gland morphology'),
(731006, 'HP:0001580', 'Pigmented micronodular adrenocortical disease', 'XPO:0102492', 'abnormal parathyroid morphology', 0.45652173913043476, 7.767034997756375, 1.8830348709099076, 'UPHENO:0087376', 'abnormal endocrine gland morphology'),
(731007, 'HP:0001580', 'Pigmented micronodular adrenocortical disease', 'XPO:0102472', 'abnormal thyroid morphology', 0.4375, 7.767034997756375, 1.8433875912347935, 'UPHENO:0087376', 'abnormal endocrine gland morphology'),
(731008, 'HP:0001580', 'Pigmented micronodular adrenocortical disease', 'XPO:0128454', 'decreased size of the adrenal cortex', 0.5185185185185185, 12.819732420846037, 2.5782297536606213, 'HP:0000849', 'Adrenocortical abnormality'),
(731009, 'HP:0001580', 'Pigmented micronodular adrenocortical disease', 'XPO:0101638', 'abnormal anatomical structure morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(731010, 'HP:0001580', 'Pigmented micronodular adrenocortical disease', 'XPO:0140100', 'abnormally necrotic adrenal cortex', 0.5384615384615384, 12.819732420846037, 2.62734330493638, 'HP:0000849', 'Adrenocortical abnormality'),
(731011, 'HP:0001580', 'Pigmented micronodular adrenocortical disease', 'XPO:0140949', 'abnormally necrotic parathyroid', 0.4117647058823529, 7.767034997756375, 1.7883486464974037, 'UPHENO:0087376', 'abnormal endocrine gland morphology'),
(731012, 'HP:0001580', 'Pigmented micronodular adrenocortical disease', 'XPO:0140281', 'abnormally necrotic endocrine system', 0.4318181818181818, 7.428233084304616, 1.7909902580935733, 'UPHENO:0076812', 'abnormal endocrine system morphology'),
(731013, 'HP:0001580', 'Pigmented micronodular adrenocortical disease', 'XPO:0126275', 'absent adrenal cortex', 0.5185185185185185, 12.819732420846037, 2.5782297536606213, 'HP:0000849', 'Adrenocortical abnormality'),
(731014, 'HP:0001580', 'Pigmented micronodular adrenocortical disease', 'XPO:0128819', 'decreased size of the adrenal gland', 0.4642857142857143, 11.7363164126584, 2.33431018691481, 'UPHENO:0020671', 'abnormal adrenal gland morphology'),
(731015, 'HP:0011981', 'Pigment gallstones', 'XPO:0141005', 'abnormally necrotic bile duct', 0.4262295081967213, 9.7042552034261, 2.0337747964737347, 'UPHENO:0002666', 'abnormal biliary system'),
(731016, 'HP:0011981', 'Pigment gallstones', 'XPO:0125701', 'absent biliary tree', 0.4074074074074074, 9.7042552034261, 1.9883625054923135, 'UPHENO:0002666', 'abnormal biliary system'),
(731017, 'HP:0011981', 'Pigment gallstones', 'XPO:0103284', 'absent gall bladder', 0.4166666666666667, 12.30515924801628, 2.2643210211172464, 'UPHENO:0076778', 'abnormal gallbladder morphology'),
(731018, 'HP:0011981', 'Pigment gallstones', 'XPO:0141639', 'neoplastic gall bladder', 0.42857142857142855, 12.30515924801628, 2.296440654082152, 'UPHENO:0076778', 'abnormal gallbladder morphology'),
(731019, 'HP:0011981', 'Pigment gallstones', 'XPO:0102125', 'abnormal liver and biliary system morphology', 0.41304347826086957, 8.69832224767236, 1.8954643959231987, 'UPHENO:0087100', 'abnormal hepatobiliary system morphology'),
(731020, 'HP:0011981', 'Pigment gallstones', 'XPO:0140388', 'abnormally necrotic biliary tree', 0.4406779661016949, 9.7042552034261, 2.0679582794576885, 'UPHENO:0002666', 'abnormal biliary system'),
(731021, 'HP:0011981', 'Pigment gallstones', 'XPO:0127346', 'abnormally localised biliary tree', 0.4074074074074074, 9.7042552034261, 1.9883625054923135, 'UPHENO:0002666', 'abnormal biliary system'),
(731022, 'HP:0011981', 'Pigment gallstones', 'XPO:0129215', 'decreased size of the bile duct', 0.4126984126984127, 9.7042552034261, 2.0012323000776955, 'UPHENO:0002666', 'abnormal biliary system'),
(731023, 'HP:0011981', 'Pigment gallstones', 'XPO:0130806', 'increased size of the biliary tree', 0.4262295081967213, 9.7042552034261, 2.0337747964737347, 'UPHENO:0002666', 'abnormal biliary system'),
(731024, 'HP:0011981', 'Pigment gallstones', 'XPO:0130691', 'increased size of the bile duct', 0.4126984126984127, 9.7042552034261, 2.0012323000776955, 'UPHENO:0002666', 'abnormal biliary system'),
(731025, 'HP:0011981', 'Pigment gallstones', 'XPO:0102825', 'abnormal bile duct morphology', 0.4727272727272727, 9.7042552034261, 2.1418370844126, 'UPHENO:0002666', 'abnormal biliary system'),
(731026, 'HP:0011981', 'Pigment gallstones', 'XPO:0102211', 'abnormal biliary tree morphology', 0.48148148148148145, 9.7042552034261, 2.1615779356803153, 'UPHENO:0002666', 'abnormal biliary system'),
(731027, 'HP:0011981', 'Pigment gallstones', 'XPO:0129330', 'decreased size of the biliary tree', 0.4262295081967213, 9.7042552034261, 2.0337747964737347, 'UPHENO:0002666', 'abnormal biliary system'),
(731028, 'HP:0011981', 'Pigment gallstones', 'XPO:0100579', 'abnormal biliary tree', 0.5, 9.7042552034261, 2.202754548676055, 'UPHENO:0002666', 'abnormal biliary system'),
(731029, 'HP:0011981', 'Pigment gallstones', 'XPO:0101193', 'abnormal bile duct', 0.4888888888888889, 9.7042552034261, 2.1781419935112596, 'UPHENO:0002666', 'abnormal biliary system'),
(731030, 'HP:0011981', 'Pigment gallstones', 'XPO:0101386', 'abnormal gall bladder', 0.4528301886792453, 11.7363164126584, 2.305332595428136, 'HP:0005264', 'Abnormality of the gallbladder'),
(731031, 'HP:0011981', 'Pigment gallstones', 'XPO:0103018', 'abnormal gall bladder morphology', 0.44776119402985076, 12.30515924801628, 2.347290522628, 'UPHENO:0076778', 'abnormal gallbladder morphology'),
(731032, 'HP:0011981', 'Pigment gallstones', 'XPO:0141609', 'metaplastic gall bladder', 0.42105263157894735, 11.7363164126584, 2.2229725393249935, 'HP:0005264', 'Abnormality of the gallbladder'),
(731033, 'HP:0004943', 'Accelerated atherosclerosis', 'XPO:0102802', 'abnormal arteria subclavia morphology', 0.40350877192982454, 6.65602285090012, 1.6388299504535415, 'HP:0025015', 'Abnormal vascular morphology'),
(731034, 'HP:0004943', 'Accelerated atherosclerosis', 'XPO:0101955', 'abnormal intersomitic artery morphology', 0.40350877192982454, 6.65602285090012, 1.6388299504535415, 'HP:0025015', 'Abnormal vascular morphology'),
(731035, 'HP:0004943', 'Accelerated atherosclerosis', 'XPO:0102425', 'abnormal omphalomesenteric vein morphology', 0.4067796610169492, 7.803720102857406, 1.7816830857679173, 'HP:0033353', 'Abnormal blood vessel morphology'),
(731036, 'HP:0004943', 'Accelerated atherosclerosis', 'XPO:0102554', 'abnormal lymph vessel morphology', 0.4423076923076923, 6.65602285090012, 1.7158117924553669, 'HP:0025015', 'Abnormal vascular morphology'),
(731037, 'HP:0004943', 'Accelerated atherosclerosis', 'XPO:0102889', 'abnormal coeliaco-mesenteric artery morphology', 0.41818181818181815, 6.65602285090012, 1.6683607936082474, 'HP:0025015', 'Abnormal vascular morphology'),
(731038, 'HP:0004943', 'Accelerated atherosclerosis', 'XPO:0101675', 'abnormal vein morphology', 0.4897959183673469, 7.803720102857406, 1.955052494042237, 'HP:0033353', 'Abnormal blood vessel morphology'),
(731039, 'HP:0004943', 'Accelerated atherosclerosis', 'XPO:0140809', 'abnormally necrotic truncus arteriosus', 0.4423076923076923, 6.65602285090012, 1.7158117924553669, 'HP:0025015', 'Abnormal vascular morphology'),
(731040, 'HP:0004943', 'Accelerated atherosclerosis', 'XPO:0140666', 'abnormally necrotic occipitovertebral artery', 0.40350877192982454, 6.65602285090012, 1.6388299504535415, 'HP:0025015', 'Abnormal vascular morphology'),
(731041, 'HP:0004943', 'Accelerated atherosclerosis', 'XPO:0101956', 'abnormal intersomitic vessel morphology', 0.46, 6.65602285090012, 1.7497915622765061, 'HP:0025015', 'Abnormal vascular morphology'),
(731042, 'HP:0004943', 'Accelerated atherosclerosis', 'XPO:0102709', 'abnormal ventral abdominal vein morphology', 0.42857142857142855, 7.803720102857406, 1.828784151465988, 'HP:0033353', 'Abnormal blood vessel morphology'),
(731043, 'HP:0004943', 'Accelerated atherosclerosis', 'XPO:0103119', 'abnormal epigastric artery morphology', 0.41818181818181815, 6.65602285090012, 1.6683607936082474, 'HP:0025015', 'Abnormal vascular morphology'),
(731044, 'HP:0004943', 'Accelerated atherosclerosis', 'XPO:0141260', 'abnormally necrotic dorsal longitudinal anastomosing vessel - left branch', 0.41818181818181815, 6.65602285090012, 1.6683607936082474, 'HP:0025015', 'Abnormal vascular morphology'),
(731045, 'HP:0004943', 'Accelerated atherosclerosis', 'XPO:0139990', 'abnormally necrotic cardiovascular system', 0.41304347826086957, 5.9590888072311134, 1.5688730886225806, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(731046, 'HP:0004943', 'Accelerated atherosclerosis', 'XPO:0102421', 'abnormal occipitovertebral artery morphology', 0.46, 6.65602285090012, 1.7497915622765061, 'HP:0025015', 'Abnormal vascular morphology'),
(731047, 'HP:0004943', 'Accelerated atherosclerosis', 'XPO:0101769', 'abnormal cardinal vein morphology', 0.4528301886792453, 7.803720102857406, 1.8798297919165285, 'HP:0033353', 'Abnormal blood vessel morphology'),
(731048, 'HP:0004943', 'Accelerated atherosclerosis', 'XPO:0101685', 'abnormal head vasculature morphology', 0.4339622641509434, 6.65602285090012, 1.6995478065112006, 'HP:0025015', 'Abnormal vascular morphology'),
(731049, 'HP:0004943', 'Accelerated atherosclerosis', 'XPO:0129296', 'decreased size of the truncus arteriosus', 0.42592592592592593, 6.65602285090012, 1.683737715843461, 'HP:0025015', 'Abnormal vascular morphology'),
(731050, 'HP:0004943', 'Accelerated atherosclerosis', 'XPO:0102251', 'abnormal interrenal vein morphology', 0.42857142857142855, 7.803720102857406, 1.828784151465988, 'HP:0033353', 'Abnormal blood vessel morphology'),
(731051, 'HP:0004943', 'Accelerated atherosclerosis', 'XPO:0102113', 'abnormal anatomical line morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(731052, 'HP:0004943', 'Accelerated atherosclerosis', 'XPO:0128922', 'decreased size of the dorsal longitudinal anastomosing vessel', 0.42592592592592593, 6.65602285090012, 1.683737715843461, 'HP:0025015', 'Abnormal vascular morphology'),
(731053, 'HP:0004943', 'Accelerated atherosclerosis', 'XPO:0130851', 'increased size of the dorsal longitudinal anastomosing vessel - right branch', 0.40350877192982454, 6.65602285090012, 1.6388299504535415, 'HP:0025015', 'Abnormal vascular morphology'),
(731054, 'HP:0004943', 'Accelerated atherosclerosis', 'XPO:0102935', 'abnormal bulbous arteriosis morphology', 0.4418604651162791, 5.9590888072311134, 1.6226785732338835, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(731055, 'HP:0004943', 'Accelerated atherosclerosis', 'XPO:0102612', 'abnormal dorsal longitudinal anastomosing vessel - left branch morphology', 0.4791666666666667, 6.65602285090012, 1.7858735349186892, 'HP:0025015', 'Abnormal vascular morphology'),
(731056, 'HP:0004943', 'Accelerated atherosclerosis', 'XPO:0101916', 'abnormal tail vasculature morphology', 0.4423076923076923, 6.65602285090012, 1.7158117924553669, 'HP:0025015', 'Abnormal vascular morphology'),
(731057, 'HP:0004943', 'Accelerated atherosclerosis', 'XPO:0140755', 'abnormally necrotic vascular plexus', 0.4339622641509434, 6.65602285090012, 1.6995478065112006, 'HP:0025015', 'Abnormal vascular morphology'),
(731058, 'HP:0004943', 'Accelerated atherosclerosis', 'XPO:0101829', 'abnormal subclavian vein morphology', 0.42857142857142855, 7.803720102857406, 1.828784151465988, 'HP:0033353', 'Abnormal blood vessel morphology'),
(731059, 'HP:0004943', 'Accelerated atherosclerosis', 'XPO:0102800', 'abnormal circulating cell morphology', 0.4222222222222222, 5.9590888072311134, 1.5862092291399303, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(731060, 'HP:0004943', 'Accelerated atherosclerosis', 'XPO:0102993', 'abnormal musculoabdominal vein morphology', 0.42857142857142855, 7.803720102857406, 1.828784151465988, 'HP:0033353', 'Abnormal blood vessel morphology'),
(731061, 'HP:0004943', 'Accelerated atherosclerosis', 'XPO:0102683', 'abnormal intersomitic vein morphology', 0.4423076923076923, 6.65602285090012, 1.7158117924553669, 'HP:0025015', 'Abnormal vascular morphology'),
(731062, 'HP:0004943', 'Accelerated atherosclerosis', 'XPO:0139730', 'abnormally necrotic vein', 0.43636363636363634, 7.803720102857406, 1.8453345716283722, 'HP:0033353', 'Abnormal blood vessel morphology'),
(731063, 'HP:0004943', 'Accelerated atherosclerosis', 'XPO:0103189', 'abnormal Jacobsons vein morphology', 0.47058823529411764, 7.803720102857406, 1.9163347494456433, 'HP:0033353', 'Abnormal blood vessel morphology'),
(731064, 'HP:0004943', 'Accelerated atherosclerosis', 'XPO:0102575', 'abnormal caudal vein morphology', 0.4067796610169492, 7.803720102857406, 1.7816830857679173, 'HP:0033353', 'Abnormal blood vessel morphology'),
(731065, 'HP:0004943', 'Accelerated atherosclerosis', 'XPO:0101686', 'abnormal blood vessel morphology', 0.5227272727272727, 6.65602285090012, 1.865284072751769, 'HP:0025015', 'Abnormal vascular morphology'),
(731066, 'HP:0004943', 'Accelerated atherosclerosis', 'XPO:0101774', 'abnormal paired dorsal aorta morphology', 0.45614035087719296, 8.750570396338642, 1.9978709295050783, 'HP:0011004', 'Abnormal systemic arterial morphology'),
(731067, 'HP:0004943', 'Accelerated atherosclerosis', 'XPO:0102962', 'abnormal postcaval vein morphology', 0.42857142857142855, 7.803720102857406, 1.828784151465988, 'HP:0033353', 'Abnormal blood vessel morphology'),
(731068, 'HP:0004943', 'Accelerated atherosclerosis', 'XPO:0103212', 'abnormal cutaneous magnus morphology', 0.42857142857142855, 7.803720102857406, 1.828784151465988, 'HP:0033353', 'Abnormal blood vessel morphology'),
(731069, 'HP:0004943', 'Accelerated atherosclerosis', 'XPO:0101845', 'abnormal right channel of ventral aorta morphology', 0.41818181818181815, 6.65602285090012, 1.6683607936082474, 'HP:0025015', 'Abnormal vascular morphology'),
(731070, 'HP:0004943', 'Accelerated atherosclerosis', 'XPO:0101995', 'abnormal cardiovascular system morphology', 0.475, 5.9590888072311134, 1.6824289534582966, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(731071, 'HP:0004943', 'Accelerated atherosclerosis', 'XPO:0101770', 'abnormal trunk vasculature morphology', 0.40425531914893614, 5.9590888072311134, 1.552093214856655, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(731072, 'HP:0004943', 'Accelerated atherosclerosis', 'XPO:0102645', 'abnormal ventral caudal lymphatic vessel morphology', 0.42592592592592593, 6.65602285090012, 1.683737715843461, 'HP:0025015', 'Abnormal vascular morphology'),
(731073, 'HP:0004943', 'Accelerated atherosclerosis', 'XPO:0128921', 'decreased size of the dorsal longitudinal anastomosing vessel - left branch', 0.40350877192982454, 6.65602285090012, 1.6388299504535415, 'HP:0025015', 'Abnormal vascular morphology'),
(731074, 'HP:0004943', 'Accelerated atherosclerosis', 'XPO:0102154', 'abnormal subinterstitial vein morphology', 0.47058823529411764, 7.803720102857406, 1.9163347494456433, 'HP:0033353', 'Abnormal blood vessel morphology'),
(731075, 'HP:0004943', 'Accelerated atherosclerosis', 'XPO:0102424', 'abnormal capillary morphology', 0.4897959183673469, 7.803720102857406, 1.955052494042237, 'HP:0033353', 'Abnormal blood vessel morphology'),
(731076, 'HP:0004943', 'Accelerated atherosclerosis', 'XPO:0102363', 'abnormal arterial endothelium morphology', 0.40350877192982454, 6.65602285090012, 1.6388299504535415, 'HP:0025015', 'Abnormal vascular morphology'),
(731077, 'HP:0004943', 'Accelerated atherosclerosis', 'XPO:0102838', 'abnormal ischiadic vein morphology', 0.47058823529411764, 7.803720102857406, 1.9163347494456433, 'HP:0033353', 'Abnormal blood vessel morphology'),
(731078, 'HP:0004943', 'Accelerated atherosclerosis', 'XPO:0140152', 'abnormally necrotic capillary', 0.43636363636363634, 7.803720102857406, 1.8453345716283722, 'HP:0033353', 'Abnormal blood vessel morphology'),
(731079, 'HP:0004943', 'Accelerated atherosclerosis', 'XPO:0140207', 'abnormally necrotic branchial vein', 0.41379310344827586, 7.803720102857406, 1.7969767833233308, 'HP:0033353', 'Abnormal blood vessel morphology'),
(731080, 'HP:0004943', 'Accelerated atherosclerosis', 'XPO:0130150', 'increased size of the capillary', 0.42105263157894735, 7.803720102857406, 1.8126712016837594, 'HP:0033353', 'Abnormal blood vessel morphology'),
(731081, 'HP:0004943', 'Accelerated atherosclerosis', 'XPO:0101919', 'abnormal heart primordium morphology', 0.4222222222222222, 5.9590888072311134, 1.5862092291399303, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(731082, 'HP:0004943', 'Accelerated atherosclerosis', 'XPO:0130772', 'increased size of the truncus arteriosus', 0.42592592592592593, 6.65602285090012, 1.683737715843461, 'HP:0025015', 'Abnormal vascular morphology'),
(731083, 'HP:0004943', 'Accelerated atherosclerosis', 'XPO:0130399', 'increased size of the dorsal longitudinal anastomosing vessel - left branch', 0.40350877192982454, 6.65602285090012, 1.6388299504535415, 'HP:0025015', 'Abnormal vascular morphology'),
(731084, 'HP:0004943', 'Accelerated atherosclerosis', 'XPO:0102553', 'abnormal dorsal caudal lymphatic vessel morphology', 0.42592592592592593, 6.65602285090012, 1.683737715843461, 'HP:0025015', 'Abnormal vascular morphology'),
(731085, 'HP:0004943', 'Accelerated atherosclerosis', 'XPO:0129377', 'decreased size of the dorsal longitudinal anastomosing vessel - right branch', 0.40350877192982454, 6.65602285090012, 1.6388299504535415, 'HP:0025015', 'Abnormal vascular morphology'),
(731086, 'HP:0004943', 'Accelerated atherosclerosis', 'XPO:0102748', 'abnormal lateral vein morphology', 0.42857142857142855, 7.803720102857406, 1.828784151465988, 'HP:0033353', 'Abnormal blood vessel morphology'),
(731087, 'HP:0004943', 'Accelerated atherosclerosis', 'XPO:0103217', 'abnormal dorsal longitudinal anastomosing vessel - right branch morphology', 0.4791666666666667, 6.65602285090012, 1.7858735349186892, 'HP:0025015', 'Abnormal vascular morphology'),
(731088, 'HP:0004943', 'Accelerated atherosclerosis', 'XPO:0140530', 'abnormally necrotic ischiadic artery', 0.40350877192982454, 6.65602285090012, 1.6388299504535415, 'HP:0025015', 'Abnormal vascular morphology'),
(731089, 'HP:0004943', 'Accelerated atherosclerosis', 'XPO:0140187', 'abnormally necrotic intersomitic vessel', 0.4107142857142857, 6.65602285090012, 1.6533976142795799, 'HP:0025015', 'Abnormal vascular morphology'),
(731090, 'HP:0004943', 'Accelerated atherosclerosis', 'XPO:0102565', 'abnormal branchial vein morphology', 0.47058823529411764, 7.803720102857406, 1.9163347494456433, 'HP:0033353', 'Abnormal blood vessel morphology'),
(731091, 'HP:0004943', 'Accelerated atherosclerosis', 'XPO:0141223', 'abnormally necrotic Jacobsons vein', 0.41379310344827586, 7.803720102857406, 1.7969767833233308, 'HP:0033353', 'Abnormal blood vessel morphology'),
(731092, 'HP:0004943', 'Accelerated atherosclerosis', 'XPO:0102570', 'abnormal duct of Cuvier morphology', 0.4067796610169492, 7.803720102857406, 1.7816830857679173, 'HP:0033353', 'Abnormal blood vessel morphology'),
(731093, 'HP:0004943', 'Accelerated atherosclerosis', 'XPO:0128028', 'decreased size of the vein', 0.42105263157894735, 7.803720102857406, 1.8126712016837594, 'HP:0033353', 'Abnormal blood vessel morphology'),
(731094, 'HP:0004943', 'Accelerated atherosclerosis', 'XPO:0101976', 'abnormal portion of organism substance morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(731095, 'HP:0004943', 'Accelerated atherosclerosis', 'XPO:0140735', 'abnormally necrotic lymph vessel', 0.40350877192982454, 6.65602285090012, 1.6388299504535415, 'HP:0025015', 'Abnormal vascular morphology'),
(731096, 'HP:0004943', 'Accelerated atherosclerosis', 'XPO:0101638', 'abnormal anatomical structure morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(731097, 'HP:0004943', 'Accelerated atherosclerosis', 'XPO:0139811', 'abnormally necrotic circulatory system', 0.41304347826086957, 5.9590888072311134, 1.5688730886225806, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(731098, 'HP:0004943', 'Accelerated atherosclerosis', 'XPO:0129573', 'increased size of the aorta', 0.40625, 8.750570396338642, 1.8854493426004777, 'HP:0011004', 'Abnormal systemic arterial morphology'),
(731099, 'HP:0004943', 'Accelerated atherosclerosis', 'XPO:0102311', 'abnormal left channel of ventral aorta morphology', 0.41818181818181815, 6.65602285090012, 1.6683607936082474, 'HP:0025015', 'Abnormal vascular morphology'),
(731100, 'HP:0004943', 'Accelerated atherosclerosis', 'XPO:0139723', 'abnormally necrotic blood vessel', 0.46938775510204084, 6.65602285090012, 1.7675563990696006, 'HP:0025015', 'Abnormal vascular morphology'),
(731101, 'HP:0004943', 'Accelerated atherosclerosis', 'XPO:0100054', 'abnormal blood vessel', 0.41025641025641024, 5.809304221129108, 1.5437954190396599, 'UPHENO:0002678', 'abnormal vasculature'),
(731102, 'HP:0004943', 'Accelerated atherosclerosis', 'XPO:0103215', 'abnormal truncus arteriosus morphology', 0.5, 6.65602285090012, 1.8242838116504954, 'HP:0025015', 'Abnormal vascular morphology'),
(731103, 'HP:0004943', 'Accelerated atherosclerosis', 'XPO:0101712', 'abnormal aorta morphology', 0.4727272727272727, 8.750570396338642, 2.0338714999402434, 'HP:0011004', 'Abnormal systemic arterial morphology'),
(731104, 'HP:0004943', 'Accelerated atherosclerosis', 'XPO:0101900', 'abnormal circulatory system morphology', 0.475, 5.9590888072311134, 1.6824289534582966, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(731105, 'HP:0004943', 'Accelerated atherosclerosis', 'XPO:0102329', 'abnormal caudal artery morphology', 0.4262295081967213, 8.750570396338642, 1.93125640878476, 'HP:0011004', 'Abnormal systemic arterial morphology'),
(731106, 'HP:0004943', 'Accelerated atherosclerosis', 'XPO:0141029', 'abnormally necrotic subinterstitial vein', 0.41379310344827586, 7.803720102857406, 1.7969767833233308, 'HP:0033353', 'Abnormal blood vessel morphology'),
(731107, 'HP:0004943', 'Accelerated atherosclerosis', 'XPO:0102619', 'abnormal larval aorta morphology', 0.46, 6.65602285090012, 1.7497915622765061, 'HP:0025015', 'Abnormal vascular morphology'),
(731108, 'HP:0004943', 'Accelerated atherosclerosis', 'XPO:0129508', 'increased size of the vein', 0.42105263157894735, 7.803720102857406, 1.8126712016837594, 'HP:0033353', 'Abnormal blood vessel morphology'),
(731109, 'HP:0004943', 'Accelerated atherosclerosis', 'XPO:0129510', 'increased size of the blood vessel', 0.45098039215686275, 6.65602285090012, 1.732551816109399, 'HP:0025015', 'Abnormal vascular morphology'),
(731110, 'HP:0004943', 'Accelerated atherosclerosis', 'XPO:0130014', 'increased size of the vascular plexus', 0.41818181818181815, 6.65602285090012, 1.6683607936082474, 'HP:0025015', 'Abnormal vascular morphology'),
(731111, 'HP:0004943', 'Accelerated atherosclerosis', 'XPO:0128534', 'decreased size of the vascular plexus', 0.41818181818181815, 6.65602285090012, 1.6683607936082474, 'HP:0025015', 'Abnormal vascular morphology'),
(731112, 'HP:0004943', 'Accelerated atherosclerosis', 'XPO:0141249', 'abnormally necrotic dorsal longitudinal anastomosing vessel - right branch', 0.41818181818181815, 6.65602285090012, 1.6683607936082474, 'HP:0025015', 'Abnormal vascular morphology'),
(731113, 'HP:0004943', 'Accelerated atherosclerosis', 'XPO:0128099', 'decreased size of the artery', 0.4107142857142857, 6.65602285090012, 1.6533976142795799, 'HP:0025015', 'Abnormal vascular morphology'),
(731114, 'HP:0004943', 'Accelerated atherosclerosis', 'XPO:0141554', 'abnormal blood vessel morphology in the regenerating hindlimb', 0.46, 6.65602285090012, 1.7497915622765061, 'HP:0025015', 'Abnormal vascular morphology'),
(731115, 'HP:0004943', 'Accelerated atherosclerosis', 'XPO:0102121', 'abnormal vitelline vein morphology', 0.4067796610169492, 7.803720102857406, 1.7816830857679173, 'HP:0033353', 'Abnormal blood vessel morphology'),
(731116, 'HP:0004943', 'Accelerated atherosclerosis', 'XPO:0102412', 'abnormal vascular plexus morphology', 0.48936170212765956, 6.65602285090012, 1.8047721938563548, 'HP:0025015', 'Abnormal vascular morphology'),
(731117, 'HP:0004943', 'Accelerated atherosclerosis', 'XPO:0101780', 'abnormal arteria mesenterica posterior morphology', 0.41935483870967744, 8.750570396338642, 1.9156184477014908, 'HP:0011004', 'Abnormal systemic arterial morphology'),
(731118, 'HP:0004943', 'Accelerated atherosclerosis', 'XPO:0102904', 'abnormal lateral abdominal vein morphology', 0.42857142857142855, 7.803720102857406, 1.828784151465988, 'HP:0033353', 'Abnormal blood vessel morphology'),
(731119, 'HP:0004943', 'Accelerated atherosclerosis', 'XPO:0102875', 'abnormal vertebral artery morphology', 0.46, 6.65602285090012, 1.7497915622765061, 'HP:0025015', 'Abnormal vascular morphology'),
(731120, 'HP:0004943', 'Accelerated atherosclerosis', 'XPO:0128093', 'decreased size of the aorta', 0.40625, 8.750570396338642, 1.8854493426004777, 'HP:0011004', 'Abnormal systemic arterial morphology'),
(731121, 'HP:0004943', 'Accelerated atherosclerosis', 'XPO:0139803', 'abnormally necrotic aorta', 0.41935483870967744, 8.750570396338642, 1.9156184477014908, 'HP:0011004', 'Abnormal systemic arterial morphology'),
(731122, 'HP:0004943', 'Accelerated atherosclerosis', 'XPO:0101711', 'abnormal dorsal aorta morphology', 0.41935483870967744, 8.750570396338642, 1.9156184477014908, 'HP:0011004', 'Abnormal systemic arterial morphology'),
(731123, 'HP:0004943', 'Accelerated atherosclerosis', 'XPO:0128030', 'decreased size of the blood vessel', 0.45098039215686275, 6.65602285090012, 1.732551816109399, 'HP:0025015', 'Abnormal vascular morphology'),
(731124, 'HP:0004943', 'Accelerated atherosclerosis', 'XPO:0102613', 'abnormal dorsal longitudinal anastomosing vessel morphology', 0.5, 6.65602285090012, 1.8242838116504954, 'HP:0025015', 'Abnormal vascular morphology'),
(731125, 'HP:0004943', 'Accelerated atherosclerosis', 'XPO:0101724', 'abnormal venous endothelium morphology', 0.40350877192982454, 6.65602285090012, 1.6388299504535415, 'HP:0025015', 'Abnormal vascular morphology'),
(731126, 'HP:0004943', 'Accelerated atherosclerosis', 'XPO:0101840', 'abnormal ventral aorta morphology', 0.41935483870967744, 8.750570396338642, 1.9156184477014908, 'HP:0011004', 'Abnormal systemic arterial morphology'),
(731127, 'HP:0004943', 'Accelerated atherosclerosis', 'XPO:0103063', 'abnormal ischiadic artery morphology', 0.46, 6.65602285090012, 1.7497915622765061, 'HP:0025015', 'Abnormal vascular morphology'),
(731128, 'HP:0004943', 'Accelerated atherosclerosis', 'XPO:0141328', 'edematous circulatory system', 0.4418604651162791, 5.9590888072311134, 1.6226785732338835, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(731129, 'HP:0004943', 'Accelerated atherosclerosis', 'XPO:0103091', 'abnormal arteria iliaca communis morphology', 0.43333333333333335, 8.750570396338642, 1.9472837077358327, 'HP:0011004', 'Abnormal systemic arterial morphology'),
(731130, 'HP:0004943', 'Accelerated atherosclerosis', 'XPO:0128671', 'decreased size of the capillary', 0.42105263157894735, 7.803720102857406, 1.8126712016837594, 'HP:0033353', 'Abnormal blood vessel morphology'),
(731131, 'HP:0004943', 'Accelerated atherosclerosis', 'XPO:0102291', 'abnormal anterior cardinal vein morphology', 0.42857142857142855, 7.803720102857406, 1.828784151465988, 'HP:0033353', 'Abnormal blood vessel morphology'),
(731132, 'HP:0004943', 'Accelerated atherosclerosis', 'XPO:0103156', 'abnormal ventral blood island border morphology', 0.4107142857142857, 6.65602285090012, 1.6533976142795799, 'HP:0025015', 'Abnormal vascular morphology'),
(731133, 'HP:0004943', 'Accelerated atherosclerosis', 'XPO:0139829', 'abnormally necrotic artery', 0.42592592592592593, 6.65602285090012, 1.683737715843461, 'HP:0025015', 'Abnormal vascular morphology'),
(731134, 'HP:0004943', 'Accelerated atherosclerosis', 'XPO:0102849', 'abnormal tail vein morphology', 0.42105263157894735, 7.803720102857406, 1.8126712016837594, 'HP:0033353', 'Abnormal blood vessel morphology'),
(731135, 'HP:0004943', 'Accelerated atherosclerosis', 'XPO:0101713', 'abnormal anatomical entity in vitro morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(731136, 'HP:0004943', 'Accelerated atherosclerosis', 'XPO:0141079', 'abnormally necrotic ischiadic vein', 0.41379310344827586, 7.803720102857406, 1.7969767833233308, 'HP:0033353', 'Abnormal blood vessel morphology'),
(731137, 'HP:0004943', 'Accelerated atherosclerosis', 'XPO:0130400', 'increased size of the dorsal longitudinal anastomosing vessel', 0.42592592592592593, 6.65602285090012, 1.683737715843461, 'HP:0025015', 'Abnormal vascular morphology'),
(731138, 'HP:0004943', 'Accelerated atherosclerosis', 'XPO:0102532', 'abnormal angioblast morphology', 0.4222222222222222, 5.9590888072311134, 1.5862092291399303, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(731139, 'HP:0004943', 'Accelerated atherosclerosis', 'XPO:0140595', 'abnormally necrotic dorsal longitudinal anastomosing vessel', 0.4423076923076923, 6.65602285090012, 1.7158117924553669, 'HP:0025015', 'Abnormal vascular morphology'),
(731140, 'HP:0004943', 'Accelerated atherosclerosis', 'XPO:0140800', 'abnormally necrotic larval aorta', 0.40350877192982454, 6.65602285090012, 1.6388299504535415, 'HP:0025015', 'Abnormal vascular morphology'),
(731141, 'HP:0004943', 'Accelerated atherosclerosis', 'XPO:0102355', 'abnormal lateral postcardinal vein morphology', 0.42857142857142855, 7.803720102857406, 1.828784151465988, 'HP:0033353', 'Abnormal blood vessel morphology'),
(731142, 'HP:0004943', 'Accelerated atherosclerosis', 'XPO:0101154', 'abnormal external carotid artery', 0.45614035087719296, 8.750570396338642, 1.9978709295050783, 'HP:0011004', 'Abnormal systemic arterial morphology'),
(731143, 'HP:0004943', 'Accelerated atherosclerosis', 'XPO:0141046', 'abnormally necrotic vertebral artery', 0.40350877192982454, 6.65602285090012, 1.6388299504535415, 'HP:0025015', 'Abnormal vascular morphology'),
(731144, 'HP:0004943', 'Accelerated atherosclerosis', 'XPO:0102284', 'abnormal medial cardinal vein morphology', 0.42857142857142855, 7.803720102857406, 1.828784151465988, 'HP:0033353', 'Abnormal blood vessel morphology'),
(731145, 'HP:0004943', 'Accelerated atherosclerosis', 'XPO:0129579', 'increased size of the artery', 0.4107142857142857, 6.65602285090012, 1.6533976142795799, 'HP:0025015', 'Abnormal vascular morphology'),
(731146, 'HP:0004943', 'Accelerated atherosclerosis', 'XPO:0102166', 'abnormal medial abdominal vein morphology', 0.42857142857142855, 7.803720102857406, 1.828784151465988, 'HP:0033353', 'Abnormal blood vessel morphology'),
(731147, 'HP:0004943', 'Accelerated atherosclerosis', 'XPO:0101708', 'abnormal artery morphology', 0.4791666666666667, 6.65602285090012, 1.7858735349186892, 'HP:0025015', 'Abnormal vascular morphology'),
(731148, 'HP:0008208', 'Parathyroid hyperplasia', 'XPO:0139937', 'abnormally necrotic ultimobranchial body', 0.4117647058823529, 7.767034997756375, 1.7883486464974037, 'UPHENO:0087376', 'abnormal endocrine gland morphology'),
(731149, 'HP:0008208', 'Parathyroid hyperplasia', 'XPO:0130595', 'increased size of the postero-dorsal region', 0.41025641025641024, 5.972749669260594, 1.565362206861726, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(731150, 'HP:0008208', 'Parathyroid hyperplasia', 'XPO:0129982', 'increased size of the anatomical line', 0.4444444444444444, 5.972749669260594, 1.629280641436663, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(731151, 'HP:0008208', 'Parathyroid hyperplasia', 'XPO:0129988', 'increased size of the dorso-lateral region', 0.41025641025641024, 5.972749669260594, 1.565362206861726, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(731152, 'HP:0008208', 'Parathyroid hyperplasia', 'XPO:0130623', 'increased size of the ventro-lateral region', 0.41025641025641024, 5.972749669260594, 1.565362206861726, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(731153, 'HP:0008208', 'Parathyroid hyperplasia', 'XPO:0128826', 'decreased size of the parathyroid', 0.5, 13.257853533237922, 2.5746702248286013, 'UPHENO:0076796', 'abnormal parathyroid gland morphology'),
(731154, 'HP:0008208', 'Parathyroid hyperplasia', 'XPO:0129551', 'increased size of the cell part', 0.4186046511627907, 5.972749669260594, 1.5812086490351311, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(731155, 'HP:0008208', 'Parathyroid hyperplasia', 'XPO:0130401', 'increased size of the posterior region', 0.41025641025641024, 5.972749669260594, 1.565362206861726, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(731156, 'HP:0008208', 'Parathyroid hyperplasia', 'XPO:0129582', 'increased size of the portion of organism substance', 0.4444444444444444, 5.972749669260594, 1.629280641436663, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(731157, 'HP:0008208', 'Parathyroid hyperplasia', 'XPO:0102655', 'abnormal ultimobranchial body morphology', 0.45652173913043476, 7.767034997756375, 1.8830348709099076, 'UPHENO:0087376', 'abnormal endocrine gland morphology'),
(731158, 'HP:0008208', 'Parathyroid hyperplasia', 'XPO:0130552', 'increased size of the ventral region', 0.41025641025641024, 5.972749669260594, 1.565362206861726, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(731159, 'HP:0008208', 'Parathyroid hyperplasia', 'XPO:0129487', 'increased size of the anatomical structure', 0.4444444444444444, 5.972749669260594, 1.629280641436663, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(731160, 'HP:0008208', 'Parathyroid hyperplasia', 'XPO:0128253', 'decreased size of the ultimobranchial body', 0.4230769230769231, 7.767034997756375, 1.81274743642945, 'UPHENO:0087376', 'abnormal endocrine gland morphology'),
(731161, 'HP:0008208', 'Parathyroid hyperplasia', 'XPO:0102492', 'abnormal parathyroid morphology', 0.5555555555555556, 13.257853533237922, 2.713940711425395, 'UPHENO:0076796', 'abnormal parathyroid gland morphology'),
(731162, 'HP:0008208', 'Parathyroid hyperplasia', 'XPO:0101835', 'abnormal endocrine cell morphology', 0.40425531914893614, 7.428233084304616, 1.7328885527373792, 'UPHENO:0076812', 'abnormal endocrine system morphology'),
(731163, 'HP:0008208', 'Parathyroid hyperplasia', 'XPO:0102472', 'abnormal thyroid morphology', 0.4117647058823529, 7.767034997756375, 1.7883486464974037, 'UPHENO:0087376', 'abnormal endocrine gland morphology'),
(731164, 'HP:0008208', 'Parathyroid hyperplasia', 'XPO:0129733', 'increased size of the ultimobranchial body', 0.48, 7.767034997756375, 1.93084872502303, 'UPHENO:0087376', 'abnormal endocrine gland morphology'),
(731165, 'HP:0008208', 'Parathyroid hyperplasia', 'XPO:0130304', 'increased size of the parathyroid', 0.5918367346938775, 15.627087342903641, 3.041164965239491, 'UPHENO:0001191', 'increased size of the parathyroid gland'),
(731166, 'HP:0008208', 'Parathyroid hyperplasia', 'XPO:0130865', 'increased size of the antero-dorsal region', 0.41025641025641024, 5.972749669260594, 1.565362206861726, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(731167, 'HP:0008208', 'Parathyroid hyperplasia', 'XPO:0140949', 'abnormally necrotic parathyroid', 0.5, 13.257853533237922, 2.5746702248286013, 'UPHENO:0076796', 'abnormal parathyroid gland morphology'),
(731168, 'HP:0008208', 'Parathyroid hyperplasia', 'XPO:0101857', 'abnormal endocrine system morphology', 0.4523809523809524, 7.428233084304616, 1.8331369717469073, 'UPHENO:0076812', 'abnormal endocrine system morphology'),
(731169, 'HP:0008208', 'Parathyroid hyperplasia', 'XPO:0140281', 'abnormally necrotic endocrine system', 0.40425531914893614, 7.428233084304616, 1.7328885527373792, 'UPHENO:0076812', 'abnormal endocrine system morphology'),
(731170, 'HP:0008208', 'Parathyroid hyperplasia', 'XPO:0129735', 'increased size of the endocrine system', 0.4782608695652174, 7.428233084304616, 1.884843021111478, 'UPHENO:0076812', 'abnormal endocrine system morphology'),
(731171, 'HP:0008208', 'Parathyroid hyperplasia', 'XPO:0101561', 'abnormal adrenal cortex', 0.40384615384615385, 7.767034997756375, 1.7710695103898046, 'UPHENO:0087376', 'abnormal endocrine gland morphology'),
(731172, 'HP:0008208', 'Parathyroid hyperplasia', 'XPO:0128255', 'decreased size of the endocrine system', 0.4166666666666667, 7.428233084304616, 1.7592888104175097, 'UPHENO:0076812', 'abnormal endocrine system morphology'),
(731173, 'HP:0008208', 'Parathyroid hyperplasia', 'XPO:0130532', 'increased size of the thyroid', 0.41379310344827586, 7.767034997756375, 1.7927480348094047, 'UPHENO:0087376', 'abnormal endocrine gland morphology'),
(731174, 'HP:0008208', 'Parathyroid hyperplasia', 'XPO:0129571', 'increased size of the anatomical region', 0.42105263157894735, 5.972749669260594, 1.585825326448175, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(731175, 'HP:0008208', 'Parathyroid hyperplasia', 'XPO:0129788', 'increased size of the organ part', 0.41025641025641024, 5.972749669260594, 1.565362206861726, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(731176, 'HP:0008208', 'Parathyroid hyperplasia', 'XPO:0129517', 'increased size of the anatomical space', 0.42105263157894735, 5.972749669260594, 1.585825326448175, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(731177, 'HP:0000455', 'Broad nasal tip', 'XPO:0130079', 'increased size of the olfactory pit', 0.5, 9.467216006125252, 2.1756856397610904, 'UPHENO:0087950', 'abnormal nose morphology'),
(731178, 'HP:0000455', 'Broad nasal tip', 'XPO:0130703', 'increased size of the circumpharyngeal ridge', 0.42105263157894735, 5.972749669260594, 1.585825326448175, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(731179, 'HP:0000455', 'Broad nasal tip', 'XPO:0128440', 'decreased size of the Jacobsons organ', 0.417910447761194, 9.467216006125252, 1.989082321114877, 'UPHENO:0087950', 'abnormal nose morphology'),
(731180, 'HP:0000455', 'Broad nasal tip', 'XPO:0101634', 'abnormal head morphology', 0.42, 4.5318002188002176, 1.3796217205799897, 'UPHENO:0087907', 'abnormal head morphology'),
(731181, 'HP:0000455', 'Broad nasal tip', 'XPO:0126234', 'absent nostril', 0.4393939393939394, 9.601025046317446, 2.053930918342022, 'UPHENO:0021517', 'abnormal nose morphology'),
(731182, 'HP:0000455', 'Broad nasal tip', 'XPO:0129920', 'increased size of the Jacobsons organ', 0.46875, 9.467216006125252, 2.1065985623443333, 'UPHENO:0087950', 'abnormal nose morphology'),
(731183, 'HP:0000455', 'Broad nasal tip', 'XPO:0131638', 'increased size of the intercanthal region', 0.4444444444444444, 5.972749669260594, 1.629280641436663, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(731184, 'HP:0000455', 'Broad nasal tip', 'XPO:0103739', 'increased size of the pharyngeal region', 0.47058823529411764, 5.972749669260594, 1.6765159488388017, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(731185, 'HP:0000455', 'Broad nasal tip', 'XPO:0130640', 'increased size of the medial nasal prominence', 0.42857142857142855, 5.972749669260594, 1.5999218287949384, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(731186, 'HP:0000455', 'Broad nasal tip', 'XPO:0130787', 'increased size of the lateral nasal prominence', 0.42857142857142855, 5.972749669260594, 1.5999218287949384, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(731187, 'HP:0000455', 'Broad nasal tip', 'XPO:0130319', 'increased size of the craniofacial region', 0.42105263157894735, 5.972749669260594, 1.585825326448175, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(731188, 'HP:0000455', 'Broad nasal tip', 'XPO:0102052', 'abnormal choana morphology', 0.4393939393939394, 9.601025046317446, 2.053930918342022, 'UPHENO:0021517', 'abnormal nose morphology'),
(731189, 'HP:0000455', 'Broad nasal tip', 'XPO:0100420', 'abnormal choana', 0.5471698113207547, 9.601025046317446, 2.2920277186542393, 'UPHENO:0021517', 'abnormal nose morphology'),
(731190, 'HP:0000455', 'Broad nasal tip', 'XPO:0101483', 'abnormal nostril', 0.5686274509803921, 9.601025046317446, 2.336537266744614, 'UPHENO:0021517', 'abnormal nose morphology'),
(731191, 'HP:0000455', 'Broad nasal tip', 'XPO:0126871', 'abnormally localised choana', 0.48333333333333334, 9.601025046317446, 2.1541809206873577, 'UPHENO:0021517', 'abnormal nose morphology'),
(731192, 'HP:0000455', 'Broad nasal tip', 'XPO:0141835', 'edematous head', 0.40384615384615385, 4.5318002188002176, 1.3528303989641963, 'UPHENO:0087907', 'abnormal head morphology'),
(731193, 'HP:0000455', 'Broad nasal tip', 'XPO:0140593', 'abnormally necrotic Jacobsons organ', 0.4153846153846154, 9.467216006125252, 1.9830622480062023, 'UPHENO:0087950', 'abnormal nose morphology'),
(731194, 'HP:0000455', 'Broad nasal tip', 'XPO:0130324', 'increased size of the choana', 0.463768115942029, 9.601025046317446, 2.110130161113971, 'UPHENO:0021517', 'abnormal nose morphology'),
(731195, 'HP:0000455', 'Broad nasal tip', 'XPO:0103115', 'abnormal nostril morphology', 0.4915254237288136, 9.601025046317446, 2.1723599849293245, 'UPHENO:0021517', 'abnormal nose morphology'),
(731196, 'HP:0000455', 'Broad nasal tip', 'XPO:0133370', 'olfactory pit fused with brain', 0.4426229508196721, 9.467216006125252, 2.0470483835704494, 'UPHENO:0087950', 'abnormal nose morphology'),
(731197, 'HP:0000455', 'Broad nasal tip', 'XPO:0115526', 'abnormally incomplete structure of head', 0.4117647058823529, 4.5318002188002176, 1.3660290568695288, 'UPHENO:0087907', 'abnormal head morphology'),
(731198, 'HP:0000455', 'Broad nasal tip', 'XPO:0128599', 'decreased size of the olfactory pit', 0.45161290322580644, 9.467216006125252, 2.0677323100421026, 'UPHENO:0087950', 'abnormal nose morphology'),
(731199, 'HP:0000455', 'Broad nasal tip', 'XPO:0130295', 'increased size of the hatching gland primordium', 0.4067796610169492, 5.972749669260594, 1.5587152035573786, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(731200, 'HP:0000455', 'Broad nasal tip', 'XPO:0131462', 'increased size of the cilium in olfactory pit', 0.42857142857142855, 9.467216006125252, 2.01429349607732, 'UPHENO:0087950', 'abnormal nose morphology'),
(731201, 'HP:0000455', 'Broad nasal tip', 'XPO:0128846', 'decreased size of the choana', 0.4225352112676056, 9.601025046317446, 2.0141427820120685, 'UPHENO:0021517', 'abnormal nose morphology'),
(731202, 'HP:0000455', 'Broad nasal tip', 'XPO:0142045', 'increased size of the nasal region', 0.42105263157894735, 5.972749669260594, 1.585825326448175, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(731203, 'HP:0000455', 'Broad nasal tip', 'XPO:0102226', 'abnormal Jacobsons organ morphology', 0.45, 9.467216006125252, 2.0640366282496934, 'UPHENO:0087950', 'abnormal nose morphology'),
(731204, 'HP:0000455', 'Broad nasal tip', 'XPO:0133429', 'abnormal cilium morphology in the olfactory pit', 0.4090909090909091, 9.467216006125252, 1.967981707868695, 'UPHENO:0087950', 'abnormal nose morphology'),
(731205, 'HP:0000455', 'Broad nasal tip', 'XPO:0125246', 'absent choana', 0.4461538461538462, 9.601025046317446, 2.0696700827508563, 'UPHENO:0021517', 'abnormal nose morphology'),
(731206, 'HP:0000455', 'Broad nasal tip', 'XPO:0130273', 'increased size of the pharyngeal pouch', 0.42105263157894735, 5.972749669260594, 1.585825326448175, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(731207, 'HP:0000455', 'Broad nasal tip', 'XPO:0141839', 'edematous pharyngeal region', 0.4117647058823529, 4.5318002188002176, 1.3660290568695288, 'UPHENO:0087907', 'abnormal head morphology'),
(731208, 'HP:0000455', 'Broad nasal tip', 'XPO:0141828', 'increased width of craniofacial region', 0.4482758620689655, 9.269535338285557, 2.0384574915236024, 'UPHENO:0081800', 'increased width of the anatomical entity in independent continuant'),
(731209, 'HP:0000455', 'Broad nasal tip', 'XPO:0141298', 'abnormal intercanthal region morphology', 0.40384615384615385, 4.5318002188002176, 1.3528303989641963, 'UPHENO:0087907', 'abnormal head morphology'),
(731210, 'HP:0000455', 'Broad nasal tip', 'XPO:0102966', 'abnormal olfactory pit morphology', 0.46551724137931033, 9.467216006125252, 2.099321861629007, 'UPHENO:0087950', 'abnormal nose morphology'),
(731211, 'HP:0000455', 'Broad nasal tip', 'XPO:0103358', 'decreased size of the pharyngeal region', 0.41509433962264153, 4.6864066944795475, 1.3947404389520346, 'UPHENO:0075195', 'abnormal size of anatomical entity'),
(731212, 'HP:0000455', 'Broad nasal tip', 'XPO:0130062', 'increased size of the head region', 0.4444444444444444, 5.972749669260594, 1.629280641436663, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(731213, 'HP:0000455', 'Broad nasal tip', 'XPO:0140335', 'abnormally necrotic pharyngeal region', 0.40384615384615385, 4.5318002188002176, 1.3528303989641963, 'UPHENO:0087907', 'abnormal head morphology'),
(731214, 'HP:0000455', 'Broad nasal tip', 'XPO:0102259', 'abnormal pharyngeal region morphology', 0.42857142857142855, 4.5318002188002176, 1.3936283915633758, 'UPHENO:0087907', 'abnormal head morphology'),
(731215, 'HP:0000455', 'Broad nasal tip', 'XPO:0130934', 'increased size of the nostril', 0.49230769230769234, 9.601025046317446, 2.1740879661000143, 'UPHENO:0021517', 'abnormal nose morphology'),
(731216, 'HP:0000455', 'Broad nasal tip', 'XPO:0142059', 'abnormal nasal region morphology', 0.4117647058823529, 4.5318002188002176, 1.3660290568695288, 'UPHENO:0087907', 'abnormal head morphology'),
(731217, 'HP:0000455', 'Broad nasal tip', 'XPO:0129460', 'decreased size of the nostril', 0.4411764705882353, 9.601025046317446, 2.058092890023086, 'UPHENO:0021517', 'abnormal nose morphology'),
(731218, 'HP:0000455', 'Broad nasal tip', 'XPO:0127898', 'abnormally localised nostril', 0.47540983606557374, 9.601025046317446, 2.136450735058322, 'UPHENO:0021517', 'abnormal nose morphology'),
(731219, 'HP:0007220', 'Demyelinating motor neuropathy', 'XPO:0101204', 'abnormal peripheral nerve', 0.425531914893617, 7.318748312764234, 1.7647552193307132, 'HP:0000759', 'Abnormal peripheral nervous system morphology'),
(731220, 'HP:0007220', 'Demyelinating motor neuropathy', 'XPO:0101746', 'abnormal peripheral nervous system morphology', 0.44680851063829785, 7.318748312764234, 1.808335984645205, 'HP:0000759', 'Abnormal peripheral nervous system morphology'),
(731221, 'HP:0007220', 'Demyelinating motor neuropathy', 'XPO:0102366', 'abnormal lateral line system morphology', 0.42857142857142855, 7.318748312764234, 1.7710467017433786, 'HP:0000759', 'Abnormal peripheral nervous system morphology'),
(731222, 'HP:0007220', 'Demyelinating motor neuropathy', 'XPO:0101030', 'abnormal spinal nerve', 0.40816326530612246, 7.318748312764234, 1.7283646054266224, 'HP:0000759', 'Abnormal peripheral nervous system morphology'),
(731223, 'HP:0007220', 'Demyelinating motor neuropathy', 'XPO:0101952', 'abnormal lateral line morphology', 0.4117647058823529, 7.318748312764234, 1.7359729970343236, 'HP:0000759', 'Abnormal peripheral nervous system morphology'),
(731224, 'HP:0007220', 'Demyelinating motor neuropathy', 'XPO:0100167', 'abnormal nerve', 0.425531914893617, 7.318748312764234, 1.7647552193307132, 'HP:0000759', 'Abnormal peripheral nervous system morphology'),
(731225, 'HP:0033539', 'Bilateral apical pulmonary fibrosis', 'XPO:0101949', 'abnormal respiratory system morphology', 0.5714285714285714, 7.241224942262181, 2.034168828821693, 'HP:0012252', 'Abnormal respiratory system morphology'),
(731226, 'HP:0033539', 'Bilateral apical pulmonary fibrosis', 'XPO:0141648', 'neoplastic lung', 0.4426229508196721, 9.627087342903641, 2.064260111399415, 'UPHENO:0019970', 'abnormal lung morphology'),
(731227, 'HP:0033539', 'Bilateral apical pulmonary fibrosis', 'XPO:0141614', 'metaplastic larynx', 0.48, 7.241224942262181, 1.8643465268790154, 'HP:0012252', 'Abnormal respiratory system morphology'),
(731228, 'HP:0033539', 'Bilateral apical pulmonary fibrosis', 'XPO:0139850', 'abnormally necrotic respiratory system', 0.5106382978723404, 7.241224942262181, 1.922926618211807, 'HP:0012252', 'Abnormal respiratory system morphology'),
(731229, 'HP:0033539', 'Bilateral apical pulmonary fibrosis', 'XPO:0128535', 'decreased size of the respiratory system', 0.4897959183673469, 7.241224942262181, 1.8832743880539138, 'HP:0012252', 'Abnormal respiratory system morphology'),
(731230, 'HP:0033539', 'Bilateral apical pulmonary fibrosis', 'XPO:0130015', 'increased size of the respiratory system', 0.4897959183673469, 7.241224942262181, 1.8832743880539138, 'HP:0012252', 'Abnormal respiratory system morphology'),
(731231, 'HP:0033539', 'Bilateral apical pulmonary fibrosis', 'XPO:0141644', 'neoplastic larynx', 0.41379310344827586, 7.241224942262181, 1.7310022939400542, 'HP:0012252', 'Abnormal respiratory system morphology'),
(731232, 'HP:0033539', 'Bilateral apical pulmonary fibrosis', 'XPO:0100804', 'abnormal larynx', 0.5106382978723404, 7.241224942262181, 1.922926618211807, 'HP:0012252', 'Abnormal respiratory system morphology'),
(731233, 'HP:0033539', 'Bilateral apical pulmonary fibrosis', 'XPO:0102932', 'abnormal lung morphology', 0.46551724137931033, 9.627087342903641, 2.116973108564721, 'UPHENO:0019970', 'abnormal lung morphology'),
(731234, 'HP:0033539', 'Bilateral apical pulmonary fibrosis', 'XPO:0100210', 'abnormal pulmonary artery', 0.47368421052631576, 9.627087342903641, 2.135462307719618, 'UPHENO:0019970', 'abnormal lung morphology'),
(731235, 'HP:0033539', 'Bilateral apical pulmonary fibrosis', 'XPO:0126197', 'absent larynx', 0.41379310344827586, 7.241224942262181, 1.7310022939400542, 'HP:0012252', 'Abnormal respiratory system morphology'),
(731236, 'HP:0033539', 'Bilateral apical pulmonary fibrosis', 'XPO:0102436', 'abnormal larynx morphology', 0.43636363636363634, 7.241224942262181, 1.777584666769093, 'HP:0012252', 'Abnormal respiratory system morphology'),
(731237, 'HP:0033539', 'Bilateral apical pulmonary fibrosis', 'XPO:0101548', 'abnormal pulmonary vein', 0.47368421052631576, 9.627087342903641, 2.135462307719618, 'UPHENO:0019970', 'abnormal lung morphology'),
(731238, 'HP:0033539', 'Bilateral apical pulmonary fibrosis', 'XPO:0100586', 'abnormal thyroid primordium', 0.43636363636363634, 7.241224942262181, 1.777584666769093, 'HP:0012252', 'Abnormal respiratory system morphology'),
(731239, 'HP:0033539', 'Bilateral apical pulmonary fibrosis', 'XPO:0101036', 'abnormal pharynx', 0.47058823529411764, 7.241224942262181, 1.8459781328463531, 'HP:0012252', 'Abnormal respiratory system morphology'),
(731240, 'HP:0033539', 'Bilateral apical pulmonary fibrosis', 'XPO:0127882', 'abnormally localised pulmonary vein', 0.40298507462686567, 9.627087342903641, 1.9696630451220274, 'UPHENO:0019970', 'abnormal lung morphology'),
(731241, 'HP:0033539', 'Bilateral apical pulmonary fibrosis', 'XPO:0127859', 'abnormally localised larynx', 0.42105263157894735, 7.241224942262181, 1.746120504946495, 'HP:0012252', 'Abnormal respiratory system morphology'),
(731242, 'HP:0033539', 'Bilateral apical pulmonary fibrosis', 'XPO:0141593', 'edematous lung', 0.4426229508196721, 9.627087342903641, 2.064260111399415, 'UPHENO:0019970', 'abnormal lung morphology'),
(731243, 'HP:0033539', 'Bilateral apical pulmonary fibrosis', 'XPO:0102668', 'abnormal pharynx morphology', 0.4067796610169492, 7.241224942262181, 1.7162700916117157, 'HP:0012252', 'Abnormal respiratory system morphology'),
(731244, 'HP:0033539', 'Bilateral apical pulmonary fibrosis', 'XPO:0100875', 'abnormal oropharynx', 0.4444444444444444, 7.241224942262181, 1.793968281927239, 'HP:0012252', 'Abnormal respiratory system morphology'),
(731245, 'HP:0033539', 'Bilateral apical pulmonary fibrosis', 'XPO:0101329', 'abnormal pharyngeal epithelium', 0.46153846153846156, 7.241224942262181, 1.8281421770490451, 'HP:0012252', 'Abnormal respiratory system morphology'),
(731246, 'HP:0033539', 'Bilateral apical pulmonary fibrosis', 'XPO:0127602', 'abnormally localised pulmonary artery', 0.40298507462686567, 9.627087342903641, 1.9696630451220274, 'UPHENO:0019970', 'abnormal lung morphology'),
(731247, 'HP:0033539', 'Bilateral apical pulmonary fibrosis', 'XPO:0126855', 'abnormally localised pharynx', 0.4067796610169492, 7.241224942262181, 1.7162700916117157, 'HP:0012252', 'Abnormal respiratory system morphology'),
(731248, 'HP:3000024', 'Abnormal facial artery morphology', 'XPO:0103091', 'abnormal arteria iliaca communis morphology', 0.46875, 9.08792853179561, 2.063968628462941, 'UPHENO:0087334', 'abnormal systemic artery morphology'),
(731249, 'HP:3000024', 'Abnormal facial artery morphology', 'XPO:0140757', 'abnormally necrotic arteria iliaca communis', 0.4225352112676056, 9.08792853179561, 1.9595840890778735, 'UPHENO:0087334', 'abnormal systemic artery morphology'),
(731250, 'HP:3000024', 'Abnormal facial artery morphology', 'XPO:0139730', 'abnormally necrotic vein', 0.4032258064516129, 7.803720102857406, 1.7738831223610367, 'HP:0033353', 'Abnormal blood vessel morphology'),
(731251, 'HP:3000024', 'Abnormal facial artery morphology', 'XPO:0141159', 'abnormally necrotic posterior palatine artery', 0.4342105263157895, 11.341685124041394, 2.219161793790163, 'UPHENO:0087623', 'abnormal carotid artery segment morphology'),
(731252, 'HP:3000024', 'Abnormal facial artery morphology', 'XPO:0101780', 'abnormal arteria mesenterica posterior morphology', 0.45454545454545453, 9.08792853179561, 2.0324558064965745, 'UPHENO:0087334', 'abnormal systemic artery morphology'),
(731253, 'HP:3000024', 'Abnormal facial artery morphology', 'XPO:0103063', 'abnormal ischiadic artery morphology', 0.4727272727272727, 9.01729298920255, 2.0646356390822276, 'UPHENO:0015290', 'abnormal artery morphology in the independent continuant'),
(731254, 'HP:3000024', 'Abnormal facial artery morphology', 'XPO:0102421', 'abnormal occipitovertebral artery morphology', 0.4727272727272727, 9.01729298920255, 2.0646356390822276, 'UPHENO:0015290', 'abnormal artery morphology in the independent continuant'),
(731255, 'HP:3000024', 'Abnormal facial artery morphology', 'XPO:0101712', 'abnormal aorta morphology', 0.5084745762711864, 9.08792853179561, 2.149646624305399, 'UPHENO:0087334', 'abnormal systemic artery morphology'),
(731256, 'HP:3000024', 'Abnormal facial artery morphology', 'XPO:0102786', 'abnormal external carotid artery morphology', 0.5142857142857142, 14.124587002374458, 2.6951944856553234, 'UPHENO:0087321', 'abnormal external carotid artery morphology'),
(731257, 'HP:3000024', 'Abnormal facial artery morphology', 'XPO:0102565', 'abnormal branchial vein morphology', 0.43103448275862066, 7.803720102857406, 1.8340317494875034, 'HP:0033353', 'Abnormal blood vessel morphology'),
(731258, 'HP:3000024', 'Abnormal facial artery morphology', 'XPO:0102503', 'abnormal posterior palatine artery morphology', 0.4782608695652174, 11.341685124041394, 2.329009272149625, 'UPHENO:0087623', 'abnormal carotid artery segment morphology'),
(731259, 'HP:3000024', 'Abnormal facial artery morphology', 'XPO:0140152', 'abnormally necrotic capillary', 0.4032258064516129, 7.803720102857406, 1.7738831223610367, 'HP:0033353', 'Abnormal blood vessel morphology'),
(731260, 'HP:3000024', 'Abnormal facial artery morphology', 'XPO:0101675', 'abnormal vein morphology', 0.44642857142857145, 7.803720102857406, 1.86649500865849, 'HP:0033353', 'Abnormal blood vessel morphology'),
(731261, 'HP:3000024', 'Abnormal facial artery morphology', 'XPO:0130521', 'increased size of the posterior palatine artery', 0.4230769230769231, 11.341685124041394, 2.190526248367443, 'UPHENO:0087623', 'abnormal carotid artery segment morphology'),
(731262, 'HP:3000024', 'Abnormal facial artery morphology', 'XPO:0102424', 'abnormal capillary morphology', 0.44642857142857145, 7.803720102857406, 1.86649500865849, 'HP:0033353', 'Abnormal blood vessel morphology'),
(731263, 'HP:3000024', 'Abnormal facial artery morphology', 'XPO:0140850', 'abnormally necrotic arteria mesenterica posterior', 0.410958904109589, 9.08792853179561, 1.932554048417014, 'UPHENO:0087334', 'abnormal systemic artery morphology'),
(731264, 'HP:3000024', 'Abnormal facial artery morphology', 'XPO:0139829', 'abnormally necrotic artery', 0.4406779661016949, 9.01729298920255, 1.9934197586621973, 'UPHENO:0015290', 'abnormal artery morphology in the independent continuant'),
(731265, 'HP:3000024', 'Abnormal facial artery morphology', 'XPO:0127028', 'abnormally localised ophthalmic artery', 0.42857142857142855, 11.341685124041394, 2.2047045598033628, 'UPHENO:0087623', 'abnormal carotid artery segment morphology'),
(731266, 'HP:3000024', 'Abnormal facial artery morphology', 'XPO:0101840', 'abnormal ventral aorta morphology', 0.45454545454545453, 9.08792853179561, 2.0324558064965745, 'UPHENO:0087334', 'abnormal systemic artery morphology'),
(731267, 'HP:3000024', 'Abnormal facial artery morphology', 'XPO:0103189', 'abnormal Jacobsons vein morphology', 0.43103448275862066, 7.803720102857406, 1.8340317494875034, 'HP:0033353', 'Abnormal blood vessel morphology'),
(731268, 'HP:3000024', 'Abnormal facial artery morphology', 'XPO:0129572', 'increased size of the paired dorsal aorta', 0.4225352112676056, 9.08792853179561, 1.9595840890778735, 'UPHENO:0087334', 'abnormal systemic artery morphology'),
(731269, 'HP:3000024', 'Abnormal facial artery morphology', 'XPO:0129044', 'decreased size of the posterior palatine artery', 0.4230769230769231, 11.341685124041394, 2.190526248367443, 'UPHENO:0087623', 'abnormal carotid artery segment morphology'),
(731270, 'HP:3000024', 'Abnormal facial artery morphology', 'XPO:0129018', 'decreased size of the occipitovertebral artery', 0.40625, 9.01729298920255, 1.9139684628706755, 'UPHENO:0015290', 'abnormal artery morphology in the independent continuant'),
(731271, 'HP:3000024', 'Abnormal facial artery morphology', 'XPO:0129510', 'increased size of the blood vessel', 0.41379310344827586, 6.974839882869777, 1.6988645152534954, 'UPHENO:0087186', 'abnormal blood vessel morphology'),
(731272, 'HP:3000024', 'Abnormal facial artery morphology', 'XPO:0128210', 'decreased size of the arteria iliaca communis', 0.410958904109589, 9.08792853179561, 1.932554048417014, 'UPHENO:0087334', 'abnormal systemic artery morphology'),
(731273, 'HP:3000024', 'Abnormal facial artery morphology', 'XPO:0101769', 'abnormal cardinal vein morphology', 0.4166666666666667, 7.803720102857406, 1.8032054910234865, 'HP:0033353', 'Abnormal blood vessel morphology'),
(731274, 'HP:3000024', 'Abnormal facial artery morphology', 'XPO:0102612', 'abnormal dorsal longitudinal anastomosing vessel - left branch morphology', 0.43636363636363634, 6.974839882869777, 1.744582040015079, 'UPHENO:0087186', 'abnormal blood vessel morphology'),
(731275, 'HP:3000024', 'Abnormal facial artery morphology', 'XPO:0128030', 'decreased size of the blood vessel', 0.41379310344827586, 6.974839882869777, 1.6988645152534954, 'UPHENO:0087186', 'abnormal blood vessel morphology'),
(731276, 'HP:3000024', 'Abnormal facial artery morphology', 'XPO:0102136', 'abnormal renal artery morphology', 0.4126984126984127, 9.01729298920255, 1.9290988838005214, 'UPHENO:0015290', 'abnormal artery morphology in the independent continuant'),
(731277, 'HP:3000024', 'Abnormal facial artery morphology', 'XPO:0140595', 'abnormally necrotic dorsal longitudinal anastomosing vessel', 0.4067796610169492, 6.974839882869777, 1.6844058309093048, 'UPHENO:0087186', 'abnormal blood vessel morphology'),
(731278, 'HP:3000024', 'Abnormal facial artery morphology', 'XPO:0129349', 'decreased size of the ischiadic artery', 0.40625, 9.01729298920255, 1.9139684628706755, 'UPHENO:0015290', 'abnormal artery morphology in the independent continuant'),
(731279, 'HP:3000024', 'Abnormal facial artery morphology', 'XPO:0141046', 'abnormally necrotic vertebral artery', 0.41935483870967744, 9.01729298920255, 1.9445939028714816, 'UPHENO:0015290', 'abnormal artery morphology in the independent continuant'),
(731280, 'HP:3000024', 'Abnormal facial artery morphology', 'XPO:0102412', 'abnormal vascular plexus morphology', 0.4444444444444444, 6.974839882869777, 1.7606614770679263, 'UPHENO:0087186', 'abnormal blood vessel morphology'),
(731281, 'HP:3000024', 'Abnormal facial artery morphology', 'XPO:0139723', 'abnormally necrotic blood vessel', 0.42857142857142855, 6.974839882869777, 1.7289352482549702, 'UPHENO:0087186', 'abnormal blood vessel morphology'),
(731282, 'HP:3000024', 'Abnormal facial artery morphology', 'XPO:0129579', 'increased size of the artery', 0.4262295081967213, 9.01729298920255, 1.960468402207377, 'UPHENO:0015290', 'abnormal artery morphology in the independent continuant'),
(731283, 'HP:3000024', 'Abnormal facial artery morphology', 'XPO:0140133', 'abnormally necrotic dorsal aorta', 0.40540540540540543, 9.08792853179561, 1.9194518360010886, 'UPHENO:0087334', 'abnormal systemic artery morphology'),
(731284, 'HP:3000024', 'Abnormal facial artery morphology', 'XPO:0125393', 'absent ophthalmic artery', 0.4177215189873418, 11.341685124041394, 2.176618004586636, 'UPHENO:0087623', 'abnormal carotid artery segment morphology'),
(731285, 'HP:3000024', 'Abnormal facial artery morphology', 'XPO:0102802', 'abnormal arteria subclavia morphology', 0.4426229508196721, 9.08792853179561, 2.0056235298733567, 'UPHENO:0087334', 'abnormal systemic artery morphology'),
(731286, 'HP:3000024', 'Abnormal facial artery morphology', 'XPO:0140107', 'abnormally necrotic internal carotid artery', 0.42857142857142855, 11.341685124041394, 2.2047045598033628, 'UPHENO:0087623', 'abnormal carotid artery segment morphology'),
(731287, 'HP:3000024', 'Abnormal facial artery morphology', 'XPO:0102154', 'abnormal subinterstitial vein morphology', 0.43103448275862066, 7.803720102857406, 1.8340317494875034, 'HP:0033353', 'Abnormal blood vessel morphology'),
(731288, 'HP:3000024', 'Abnormal facial artery morphology', 'XPO:0102684', 'abnormal ophthalmic artery morphology', 0.44594594594594594, 11.341685124041394, 2.2489505333069695, 'UPHENO:0087623', 'abnormal carotid artery segment morphology'),
(731289, 'HP:3000024', 'Abnormal facial artery morphology', 'XPO:0102613', 'abnormal dorsal longitudinal anastomosing vessel morphology', 0.4528301886792453, 6.974839882869777, 1.7771938724200707, 'UPHENO:0087186', 'abnormal blood vessel morphology'),
(731290, 'HP:3000024', 'Abnormal facial artery morphology', 'XPO:0101774', 'abnormal paired dorsal aorta morphology', 0.4918032786885246, 9.08792853179561, 2.114112827742188, 'UPHENO:0087334', 'abnormal systemic artery morphology'),
(731291, 'HP:3000024', 'Abnormal facial artery morphology', 'XPO:0128092', 'decreased size of the paired dorsal aorta', 0.4225352112676056, 9.08792853179561, 1.9595840890778735, 'UPHENO:0087334', 'abnormal systemic artery morphology'),
(731292, 'HP:3000024', 'Abnormal facial artery morphology', 'XPO:0130729', 'increased size of the vertebral artery', 0.40625, 9.01729298920255, 1.9139684628706755, 'UPHENO:0015290', 'abnormal artery morphology in the independent continuant'),
(731293, 'HP:3000024', 'Abnormal facial artery morphology', 'XPO:0101845', 'abnormal right channel of ventral aorta morphology', 0.43333333333333335, 9.01729298920255, 1.976738128497156, 'UPHENO:0015290', 'abnormal artery morphology in the independent continuant'),
(731294, 'HP:3000024', 'Abnormal facial artery morphology', 'XPO:0101955', 'abnormal intersomitic artery morphology', 0.41935483870967744, 9.01729298920255, 1.9445939028714816, 'UPHENO:0015290', 'abnormal artery morphology in the independent continuant'),
(731295, 'HP:3000024', 'Abnormal facial artery morphology', 'XPO:0101916', 'abnormal tail vasculature morphology', 0.4067796610169492, 6.974839882869777, 1.6844058309093048, 'UPHENO:0087186', 'abnormal blood vessel morphology'),
(731296, 'HP:3000024', 'Abnormal facial artery morphology', 'XPO:0141008', 'abnormally necrotic external carotid artery', 0.4675324675324675, 14.124587002374458, 2.5697671128133672, 'UPHENO:0087321', 'abnormal external carotid artery morphology'),
(731297, 'HP:3000024', 'Abnormal facial artery morphology', 'XPO:0127366', 'abnormally localised external carotid artery', 0.4852941176470588, 13.819732420846037, 2.589717137313056, 'UPHENO:0004442', 'abnormal external carotid artery'),
(731298, 'HP:3000024', 'Abnormal facial artery morphology', 'XPO:0140689', 'abnormally necrotic anterior palatine artery', 0.4342105263157895, 11.341685124041394, 2.219161793790163, 'UPHENO:0087623', 'abnormal carotid artery segment morphology'),
(731299, 'HP:3000024', 'Abnormal facial artery morphology', 'XPO:0140809', 'abnormally necrotic truncus arteriosus', 0.4067796610169492, 6.974839882869777, 1.6844058309093048, 'UPHENO:0087186', 'abnormal blood vessel morphology'),
(731300, 'HP:3000024', 'Abnormal facial artery morphology', 'XPO:0141554', 'abnormal blood vessel morphology in the regenerating hindlimb', 0.42105263157894735, 6.974839882869777, 1.7137020416408788, 'UPHENO:0087186', 'abnormal blood vessel morphology'),
(731301, 'HP:3000024', 'Abnormal facial artery morphology', 'XPO:0102875', 'abnormal vertebral artery morphology', 0.4727272727272727, 9.01729298920255, 2.0646356390822276, 'UPHENO:0015290', 'abnormal artery morphology in the independent continuant'),
(731302, 'HP:3000024', 'Abnormal facial artery morphology', 'XPO:0101711', 'abnormal dorsal aorta morphology', 0.45454545454545453, 9.08792853179561, 2.0324558064965745, 'UPHENO:0087334', 'abnormal systemic artery morphology'),
(731303, 'HP:3000024', 'Abnormal facial artery morphology', 'XPO:0130820', 'increased size of the external carotid artery', 0.45569620253164556, 14.124587002374458, 2.5370298893213454, 'UPHENO:0087321', 'abnormal external carotid artery morphology'),
(731304, 'HP:3000024', 'Abnormal facial artery morphology', 'XPO:0101154', 'abnormal external carotid artery', 0.5689655172413793, 13.819732420846037, 2.804095434353853, 'UPHENO:0004442', 'abnormal external carotid artery'),
(731305, 'HP:3000024', 'Abnormal facial artery morphology', 'XPO:0130824', 'increased size of the ischiadic artery', 0.40625, 9.01729298920255, 1.9139684628706755, 'UPHENO:0015290', 'abnormal artery morphology in the independent continuant'),
(731306, 'HP:3000024', 'Abnormal facial artery morphology', 'XPO:0101708', 'abnormal artery morphology', 0.49056603773584906, 9.01729298920255, 2.1032302995193715, 'UPHENO:0015290', 'abnormal artery morphology in the independent continuant'),
(731307, 'HP:3000024', 'Abnormal facial artery morphology', 'XPO:0129796', 'increased size of the internal carotid artery', 0.4177215189873418, 11.341685124041394, 2.176618004586636, 'UPHENO:0087623', 'abnormal carotid artery segment morphology'),
(731308, 'HP:3000024', 'Abnormal facial artery morphology', 'XPO:0141134', 'abnormally necrotic caudal artery', 0.4166666666666667, 9.08792853179561, 1.945928284456591, 'UPHENO:0087334', 'abnormal systemic artery morphology'),
