(415654, 'HP:0032612', 'Triphalangeal hallux', 'XPO:0100178', 'abnormal digit', 0.45901639344262296, 6.393467666143939, 1.7130984997090548, 'HP:0011297', 'Abnormal digit morphology'),
(415655, 'HP:0032612', 'Triphalangeal hallux', 'XPO:0102566', 'abnormal claw primordium morphology', 0.43529411764705883, 7.639349617137506, 1.8235580470578026, 'UPHENO:0088132', 'abnormal pedal digit morphology'),
(415656, 'HP:0032612', 'Triphalangeal hallux', 'XPO:0128670', 'decreased size of the claw primordium', 0.40217391304347827, 7.639349617137506, 1.7528112073555977, 'UPHENO:0088132', 'abnormal pedal digit morphology'),
(415657, 'HP:0032612', 'Triphalangeal hallux', 'XPO:0139979', 'abnormally necrotic claw primordium', 0.4111111111111111, 7.639349617137506, 1.7721798749753483, 'HP:0001780', 'Abnormal toe morphology'),
(415658, 'HP:0032612', 'Triphalangeal hallux', 'XPO:0101872', 'abnormal hindlimb digit 1 morphology', 0.42045454545454547, 7.639349617137506, 1.792205141952758, 'HP:0001780', 'Abnormal toe morphology'),
(415659, 'HP:0032612', 'Triphalangeal hallux', 'XPO:0141547', 'abnormal hindlimb digit morphology in the regenerating hindlimb', 0.40217391304347827, 7.639349617137506, 1.7528112073555977, 'UPHENO:0088132', 'abnormal pedal digit morphology'),
(415660, 'HP:0032612', 'Triphalangeal hallux', 'XPO:0102180', 'abnormal hindlimb digit 3 morphology', 0.42045454545454547, 7.639349617137506, 1.792205141952758, 'HP:0001780', 'Abnormal toe morphology'),
(415661, 'HP:0032612', 'Triphalangeal hallux', 'XPO:0103413', 'abnormally increased number of hindlimb digit in the regenerating hindlimb', 0.4020618556701031, 7.639349617137506, 1.7525669981997827, 'UPHENO:0088132', 'abnormal pedal digit morphology'),
(415662, 'HP:0032612', 'Triphalangeal hallux', 'XPO:0102876', 'abnormal hindlimb digit 4 morphology', 0.42045454545454547, 7.639349617137506, 1.792205141952758, 'HP:0001780', 'Abnormal toe morphology'),
(415663, 'HP:0032612', 'Triphalangeal hallux', 'XPO:0102948', 'abnormal hindlimb digit 5 morphology', 0.42045454545454547, 7.639349617137506, 1.792205141952758, 'UPHENO:0088132', 'abnormal pedal digit morphology'),
(415664, 'HP:0032612', 'Triphalangeal hallux', 'XPO:0102051', 'abnormal hindlimb digit 2 morphology', 0.42045454545454547, 7.639349617137506, 1.792205141952758, 'UPHENO:0088132', 'abnormal pedal digit morphology'),
(415665, 'HP:0031206', 'Striatal T2 hyperintensity', 'XPO:0101795', 'abnormal central amygdala morphology', 0.4146341463414634, 11.189682030596343, 2.1539787038382547, 'UPHENO:0088139', 'abnormal basal ganglion morphology'),
(415666, 'HP:0031206', 'Striatal T2 hyperintensity', 'XPO:0103178', 'abnormal dorsal pallium morphology', 0.42028985507246375, 8.02346099791745, 1.8363494384224073, 'HP:0002060', 'Abnormal cerebral morphology'),
(415667, 'HP:0031206', 'Striatal T2 hyperintensity', 'XPO:0100194', 'abnormal preoptic area', 0.4090909090909091, 6.667568321314008, 1.6515573214369805, 'HP:0100547', 'Abnormal forebrain morphology'),
(415668, 'HP:0031206', 'Striatal T2 hyperintensity', 'XPO:0100988', 'abnormal habenula', 0.4090909090909091, 6.667568321314008, 1.6515573214369805, 'HP:0100547', 'Abnormal forebrain morphology'),
(415669, 'HP:0031206', 'Striatal T2 hyperintensity', 'XPO:0101268', 'abnormal lateral hypothalamic nucleus', 0.40298507462686567, 6.667568321314008, 1.639185931352649, 'HP:0100547', 'Abnormal forebrain morphology'),
(415670, 'HP:0031206', 'Striatal T2 hyperintensity', 'XPO:0101496', 'abnormal subcommissural organ', 0.4153846153846154, 6.667568321314008, 1.6642131181731699, 'HP:0100547', 'Abnormal forebrain morphology'),
(415671, 'HP:0031206', 'Striatal T2 hyperintensity', 'XPO:0101986', 'abnormal amygdala morphology', 0.4142857142857143, 8.02346099791745, 1.8231854734408677, 'HP:0002060', 'Abnormal cerebral morphology'),
(415672, 'HP:0031206', 'Striatal T2 hyperintensity', 'XPO:0102238', 'abnormal basal forebrain morphology', 0.4264705882352941, 8.02346099791745, 1.8498027277157947, 'HP:0002060', 'Abnormal cerebral morphology'),
(415673, 'HP:0031206', 'Striatal T2 hyperintensity', 'XPO:0100729', 'abnormal thalamus', 0.421875, 6.667568321314008, 1.677164388351466, 'HP:0100547', 'Abnormal forebrain morphology'),
(415674, 'HP:0031206', 'Striatal T2 hyperintensity', 'XPO:0101123', 'abnormal third ventricle', 0.4090909090909091, 6.667568321314008, 1.6515573214369805, 'HP:0100547', 'Abnormal forebrain morphology'),
(415675, 'HP:0031206', 'Striatal T2 hyperintensity', 'XPO:0100575', 'abnormal diencephalon', 0.42857142857142855, 6.667568321314008, 1.6904228111816126, 'HP:0100547', 'Abnormal forebrain morphology'),
(415676, 'HP:0031206', 'Striatal T2 hyperintensity', 'XPO:0101293', 'abnormal posterior hypothalamus', 0.4153846153846154, 6.667568321314008, 1.6642131181731699, 'HP:0100547', 'Abnormal forebrain morphology'),
(415677, 'HP:0031206', 'Striatal T2 hyperintensity', 'XPO:0101805', 'abnormal pallidum morphology', 0.4084507042253521, 8.02346099791745, 1.810300608993995, 'HP:0002060', 'Abnormal cerebral morphology'),
(415678, 'HP:0031206', 'Striatal T2 hyperintensity', 'XPO:0101526', 'abnormal infundibulum', 0.4090909090909091, 6.667568321314008, 1.6515573214369805, 'HP:0100547', 'Abnormal forebrain morphology'),
(415679, 'HP:0031206', 'Striatal T2 hyperintensity', 'XPO:0100263', 'abnormal prethalamus', 0.4153846153846154, 6.667568321314008, 1.6642131181731699, 'HP:0100547', 'Abnormal forebrain morphology'),
(415680, 'HP:0031206', 'Striatal T2 hyperintensity', 'XPO:0103040', 'abnormal nucleus of the diagonal band morphology', 0.4027777777777778, 8.02346099791745, 1.7976851200440698, 'HP:0002060', 'Abnormal cerebral morphology'),
(415681, 'HP:0031206', 'Striatal T2 hyperintensity', 'XPO:0100656', 'abnormal ventral hypothalamic nucleus', 0.40298507462686567, 6.667568321314008, 1.639185931352649, 'HP:0100547', 'Abnormal forebrain morphology'),
(415682, 'HP:0031206', 'Striatal T2 hyperintensity', 'XPO:0101588', 'abnormal central nucleus of the thalamus', 0.40298507462686567, 6.667568321314008, 1.639185931352649, 'HP:0100547', 'Abnormal forebrain morphology'),
(415683, 'HP:0031206', 'Striatal T2 hyperintensity', 'XPO:0100971', 'abnormal prethalamus basal plate', 0.40298507462686567, 6.667568321314008, 1.639185931352649, 'HP:0100547', 'Abnormal forebrain morphology'),
(415684, 'HP:0031206', 'Striatal T2 hyperintensity', 'XPO:0102978', 'abnormal prosomere 6 morphology', 0.4027777777777778, 8.02346099791745, 1.7976851200440698, 'HP:0002060', 'Abnormal cerebral morphology'),
(415685, 'HP:0031206', 'Striatal T2 hyperintensity', 'XPO:0101851', 'abnormal basal ganglion morphology', 0.4142857142857143, 8.02346099791745, 1.8231854734408677, 'HP:0002060', 'Abnormal cerebral morphology'),
(415686, 'HP:0031206', 'Striatal T2 hyperintensity', 'XPO:0129372', 'decreased size of the anterior entopeduncular region', 0.4084507042253521, 8.02346099791745, 1.810300608993995, 'HP:0002060', 'Abnormal cerebral morphology'),
(415687, 'HP:0031206', 'Striatal T2 hyperintensity', 'XPO:0102174', 'abnormal pallium morphology', 0.4264705882352941, 8.02346099791745, 1.8498027277157947, 'HP:0002060', 'Abnormal cerebral morphology'),
(415688, 'HP:0031206', 'Striatal T2 hyperintensity', 'XPO:0100195', 'abnormal retromammillary area', 0.4153846153846154, 6.667568321314008, 1.6642131181731699, 'HP:0100547', 'Abnormal forebrain morphology'),
(415689, 'HP:0031206', 'Striatal T2 hyperintensity', 'XPO:0102007', 'abnormal anterior entopeduncular region morphology', 0.4393939393939394, 8.02346099791745, 1.8776208710622537, 'HP:0002060', 'Abnormal cerebral morphology'),
(415690, 'HP:0031206', 'Striatal T2 hyperintensity', 'XPO:0100157', 'abnormal optic tract', 0.421875, 6.667568321314008, 1.677164388351466, 'HP:0100547', 'Abnormal forebrain morphology'),
(415691, 'HP:0031206', 'Striatal T2 hyperintensity', 'XPO:0103200', 'abnormal prosomere 5 morphology', 0.4027777777777778, 8.02346099791745, 1.7976851200440698, 'HP:0002060', 'Abnormal cerebral morphology'),
(415692, 'HP:0031206', 'Striatal T2 hyperintensity', 'XPO:0101354', 'abnormal eminentia thalami', 0.421875, 6.667568321314008, 1.677164388351466, 'HP:0100547', 'Abnormal forebrain morphology'),
(415693, 'HP:0031206', 'Striatal T2 hyperintensity', 'XPO:0101595', 'abnormal prosomere 4', 0.4090909090909091, 6.667568321314008, 1.6515573214369805, 'HP:0100547', 'Abnormal forebrain morphology'),
(415694, 'HP:0031206', 'Striatal T2 hyperintensity', 'XPO:0101186', 'abnormal optic chiasm', 0.421875, 6.667568321314008, 1.677164388351466, 'HP:0100547', 'Abnormal forebrain morphology'),
(415695, 'HP:0031206', 'Striatal T2 hyperintensity', 'XPO:0101564', 'abnormal anterior thalamic nucleus', 0.40298507462686567, 6.667568321314008, 1.639185931352649, 'HP:0100547', 'Abnormal forebrain morphology'),
(415696, 'HP:0031206', 'Striatal T2 hyperintensity', 'XPO:0100962', 'abnormal dorsal thalamus', 0.4153846153846154, 6.667568321314008, 1.6642131181731699, 'HP:0100547', 'Abnormal forebrain morphology'),
(415697, 'HP:0031206', 'Striatal T2 hyperintensity', 'XPO:0115310', 'abnormally incomplete structure of forebrain', 0.40298507462686567, 6.667568321314008, 1.639185931352649, 'HP:0100547', 'Abnormal forebrain morphology'),
(415698, 'HP:0031206', 'Striatal T2 hyperintensity', 'XPO:0100698', 'abnormal optic stalk', 0.4090909090909091, 6.667568321314008, 1.6515573214369805, 'HP:0100547', 'Abnormal forebrain morphology'),
(415699, 'HP:0031206', 'Striatal T2 hyperintensity', 'XPO:0100695', 'abnormal zona limitans intrathalamica', 0.4153846153846154, 6.667568321314008, 1.6642131181731699, 'HP:0100547', 'Abnormal forebrain morphology'),
(415700, 'HP:0031206', 'Striatal T2 hyperintensity', 'XPO:0101970', 'abnormal lateral ganglionic eminence morphology', 0.4142857142857143, 8.02346099791745, 1.8231854734408677, 'HP:0002060', 'Abnormal cerebral morphology'),
(415701, 'HP:0031206', 'Striatal T2 hyperintensity', 'XPO:0100998', 'abnormal rostral tuberal region', 0.40298507462686567, 6.667568321314008, 1.639185931352649, 'HP:0100547', 'Abnormal forebrain morphology'),
(415702, 'HP:0031206', 'Striatal T2 hyperintensity', 'XPO:0140421', 'abnormally necrotic anterior entopeduncular region', 0.42028985507246375, 8.02346099791745, 1.8363494384224073, 'HP:0002060', 'Abnormal cerebral morphology'),
(415703, 'HP:0031206', 'Striatal T2 hyperintensity', 'XPO:0102760', 'abnormal dorsal pallidum morphology', 0.4027777777777778, 8.02346099791745, 1.7976851200440698, 'HP:0002060', 'Abnormal cerebral morphology'),
(415704, 'HP:0031206', 'Striatal T2 hyperintensity', 'XPO:0100590', 'abnormal hypothalamus', 0.421875, 6.667568321314008, 1.677164388351466, 'HP:0100547', 'Abnormal forebrain morphology'),
(415705, 'HP:0031206', 'Striatal T2 hyperintensity', 'XPO:0107380', 'abnormal dorsal telencephalon morphology', 0.4264705882352941, 8.02346099791745, 1.8498027277157947, 'HP:0002060', 'Abnormal cerebral morphology'),
(415706, 'HP:0031206', 'Striatal T2 hyperintensity', 'XPO:0101797', 'abnormal lateral pallium morphology', 0.42028985507246375, 8.02346099791745, 1.8363494384224073, 'HP:0002060', 'Abnormal cerebral morphology'),
(415707, 'HP:0031206', 'Striatal T2 hyperintensity', 'XPO:0100951', 'abnormal adenohypophysis', 0.40298507462686567, 6.667568321314008, 1.639185931352649, 'HP:0100547', 'Abnormal forebrain morphology'),
(415708, 'HP:0031206', 'Striatal T2 hyperintensity', 'XPO:0101987', 'abnormal striatum morphology', 0.4084507042253521, 8.02346099791745, 1.810300608993995, 'HP:0002060', 'Abnormal cerebral morphology'),
(415709, 'HP:0031206', 'Striatal T2 hyperintensity', 'XPO:0101075', 'abnormal mammilary region', 0.4090909090909091, 6.667568321314008, 1.6515573214369805, 'HP:0100547', 'Abnormal forebrain morphology'),
(415710, 'HP:0031206', 'Striatal T2 hyperintensity', 'XPO:0102200', 'abnormal telencephalon septum morphology', 0.4027777777777778, 8.02346099791745, 1.7976851200440698, 'HP:0002060', 'Abnormal cerebral morphology'),
(415711, 'HP:0031206', 'Striatal T2 hyperintensity', 'XPO:0100611', 'abnormal hypophysis', 0.4090909090909091, 6.667568321314008, 1.6515573214369805, 'HP:0100547', 'Abnormal forebrain morphology'),
(415712, 'HP:0031206', 'Striatal T2 hyperintensity', 'XPO:0102604', 'abnormal ventral pallidum morphology', 0.4027777777777778, 8.02346099791745, 1.7976851200440698, 'HP:0002060', 'Abnormal cerebral morphology'),
(415713, 'HP:0031206', 'Striatal T2 hyperintensity', 'XPO:0101053', 'abnormal anterior hypothalamus', 0.4153846153846154, 6.667568321314008, 1.6642131181731699, 'HP:0100547', 'Abnormal forebrain morphology'),
(415714, 'HP:0031206', 'Striatal T2 hyperintensity', 'XPO:0101284', 'abnormal ventromedial thalamic nucleus', 0.40298507462686567, 6.667568321314008, 1.639185931352649, 'HP:0100547', 'Abnormal forebrain morphology'),
(415715, 'HP:0031206', 'Striatal T2 hyperintensity', 'XPO:0102968', 'abnormal medial ganglionic eminence morphology', 0.4142857142857143, 8.02346099791745, 1.8231854734408677, 'HP:0002060', 'Abnormal cerebral morphology'),
(415716, 'HP:0031206', 'Striatal T2 hyperintensity', 'XPO:0102249', 'abnormal forebrain morphology', 0.4090909090909091, 6.667568321314008, 1.6515573214369805, 'HP:0100547', 'Abnormal forebrain morphology'),
(415717, 'HP:0031206', 'Striatal T2 hyperintensity', 'XPO:0102826', 'abnormal anterior commissure morphology', 0.42028985507246375, 8.02346099791745, 1.8363494384224073, 'HP:0002060', 'Abnormal cerebral morphology'),
(415718, 'HP:0031206', 'Striatal T2 hyperintensity', 'XPO:0102191', 'abnormal telencephalon morphology', 0.43283582089552236, 8.02346099791745, 1.8635560972122107, 'HP:0002060', 'Abnormal cerebral morphology'),
(415719, 'HP:0031206', 'Striatal T2 hyperintensity', 'XPO:0100315', 'abnormal neurohypophysis', 0.40298507462686567, 6.667568321314008, 1.639185931352649, 'HP:0100547', 'Abnormal forebrain morphology'),
(415720, 'HP:0031206', 'Striatal T2 hyperintensity', 'XPO:0100763', 'abnormal pretectum', 0.421875, 6.667568321314008, 1.677164388351466, 'HP:0100547', 'Abnormal forebrain morphology'),
(415721, 'HP:0031206', 'Striatal T2 hyperintensity', 'XPO:0102066', 'abnormal ventral pallium morphology', 0.42028985507246375, 8.02346099791745, 1.8363494384224073, 'HP:0002060', 'Abnormal cerebral morphology'),
(415722, 'HP:0031206', 'Striatal T2 hyperintensity', 'XPO:0139879', 'abnormally necrotic telencephalon', 0.4027777777777778, 8.02346099791745, 1.7976851200440698, 'HP:0002060', 'Abnormal cerebral morphology'),
(415723, 'HP:0031206', 'Striatal T2 hyperintensity', 'XPO:0101117', 'abnormal tuberal region', 0.4090909090909091, 6.667568321314008, 1.6515573214369805, 'HP:0100547', 'Abnormal forebrain morphology'),
(415724, 'HP:0031206', 'Striatal T2 hyperintensity', 'XPO:0102357', 'abnormal subpallium morphology', 0.4264705882352941, 8.02346099791745, 1.8498027277157947, 'HP:0002060', 'Abnormal cerebral morphology'),
(415725, 'HP:0031206', 'Striatal T2 hyperintensity', 'XPO:0101106', 'abnormal caudal tuberal region', 0.40298507462686567, 6.667568321314008, 1.639185931352649, 'HP:0100547', 'Abnormal forebrain morphology'),
(415726, 'HP:0031206', 'Striatal T2 hyperintensity', 'XPO:0102442', 'abnormal medial pallium morphology', 0.42028985507246375, 8.02346099791745, 1.8363494384224073, 'HP:0002060', 'Abnormal cerebral morphology'),
(415727, 'HP:0031206', 'Striatal T2 hyperintensity', 'XPO:0101140', 'abnormal ventrolateral thalamic nucleus', 0.40298507462686567, 6.667568321314008, 1.639185931352649, 'HP:0100547', 'Abnormal forebrain morphology'),
(415728, 'HP:0031206', 'Striatal T2 hyperintensity', 'XPO:0101663', 'abnormal central nervous system morphology', 0.40384615384615385, 5.483278994082134, 1.4880863994491305, 'HP:0002011', 'Morphological central nervous system abnormality'),
(415729, 'HP:0031206', 'Striatal T2 hyperintensity', 'XPO:0130846', 'increased size of the anterior entopeduncular region', 0.4084507042253521, 8.02346099791745, 1.810300608993995, 'HP:0002060', 'Abnormal cerebral morphology'),
(415730, 'HP:0031206', 'Striatal T2 hyperintensity', 'XPO:0142058', 'abnormal cerebrospinal fluid morphology', 0.4117647058823529, 5.483278994082134, 1.502604659339613, 'HP:0002011', 'Morphological central nervous system abnormality'),
(415731, 'HP:0009494', 'Ivory epiphyses of the 2nd finger', 'XPO:0103609', 'abnormally increased number of forelimb digit in the regenerating forelimb', 0.41007194244604317, 7.774297771301195, 1.7855031190763642, 'HP:0005918', 'Abnormal finger phalanx morphology'),
(415732, 'HP:0009494', 'Ivory epiphyses of the 2nd finger', 'XPO:0103634', 'abnormally increased number of forelimb digit', 0.42857142857142855, 7.774297771301195, 1.8253333673568306, 'HP:0005918', 'Abnormal finger phalanx morphology'),
(415733, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0101033', 'abnormal suspensorium', 0.4444444444444444, 3.9037819259951223, 1.3171993734173904, 'HP:0033127', 'Abnormality of the musculoskeletal system'),
(415734, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0131656', 'abnormal periocular mesenchyme', 0.4838709677419355, 3.868794716113063, 1.3682095757889265, 'UPHENO:0002844', 'abnormal head'),
(415735, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0101402', 'abnormal oropharyngeal papilla', 0.5357142857142857, 3.868794716113063, 1.4396418297332543, 'UPHENO:0002844', 'abnormal head'),
(415736, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0101466', 'abnormal secondary myofiber', 0.42424242424242425, 5.968280811662945, 1.591225288920281, 'UPHENO:0002816', 'abnormal musculature'),
(415737, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0101096', 'abnormal tendon', 0.41379310344827586, 3.9037819259951223, 1.270967363209146, 'HP:0033127', 'Abnormality of the musculoskeletal system'),
(415738, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0100053', 'abnormal head vasculature', 0.40540540540540543, 3.868794716113063, 1.2523698696136485, 'UPHENO:0002844', 'abnormal head'),
(415739, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0100585', 'abnormal elastica externa', 0.4444444444444444, 3.9037819259951223, 1.3171993734173904, 'HP:0033127', 'Abnormality of the musculoskeletal system'),
(415740, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0101103', 'abnormal pharyngeal mesenchyme', 0.4411764705882353, 3.868794716113063, 1.306453672460365, 'UPHENO:0002844', 'abnormal head'),
(415741, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0101467', 'abnormal alkali secreting cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(415742, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0100389', 'abnormal cranial placode', 0.4838709677419355, 3.868794716113063, 1.3682095757889265, 'UPHENO:0002844', 'abnormal head'),
(415743, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0100674', 'abnormal secondary oogonium', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(415744, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0100377', 'abnormal connective tissue', 0.4444444444444444, 3.9037819259951223, 1.3171993734173904, 'HP:0033127', 'Abnormality of the musculoskeletal system'),
(415745, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0100625', 'abnormal dorsolateral placode region', 0.45454545454545453, 3.868794716113063, 1.3261006948111689, 'UPHENO:0002844', 'abnormal head'),
(415746, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0100099', 'abnormal cranial muscle', 0.5454545454545454, 5.968280811662945, 1.8042798832971279, 'UPHENO:0002816', 'abnormal musculature'),
(415747, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0100464', 'abnormal branchial head muscle', 0.5294117647058824, 5.968280811662945, 1.7775483331720507, 'UPHENO:0002816', 'abnormal musculature'),
(415748, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0101087', 'abnormal mm. levator arcuum branchialium II', 0.5142857142857142, 5.968280811662945, 1.7519707646772533, 'UPHENO:0002816', 'abnormal musculature'),
(415749, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0100032', 'abnormal nervous system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(415750, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0101141', 'abnormal Keller explant', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(415751, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0101026', 'abnormal m. constrictor laryngis', 0.5142857142857142, 5.968280811662945, 1.7519707646772533, 'UPHENO:0002816', 'abnormal musculature'),
(415752, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0101110', 'abnormal cell-free extract', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(415753, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0100581', 'abnormal immune system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(415754, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0100416', 'abnormal ligament', 0.41379310344827586, 3.9037819259951223, 1.270967363209146, 'HP:0033127', 'Abnormality of the musculoskeletal system'),
(415755, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0101634', 'abnormal head morphology', 0.4166666666666667, 3.868794716113063, 1.2696447528267278, 'UPHENO:0002844', 'abnormal head'),
(415756, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0101046', 'abnormal mm. constrictores branchiales IV', 0.5142857142857142, 5.968280811662945, 1.7519707646772533, 'UPHENO:0002816', 'abnormal musculature'),
(415757, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0100617', 'abnormal forebrain', 0.40540540540540543, 3.868794716113063, 1.2523698696136485, 'UPHENO:0002844', 'abnormal head'),
(415758, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0100258', 'abnormal organ part', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(415759, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0101448', 'abnormal myelin accumulating cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(415760, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0101172', 'abnormal pharyngeal pouch', 0.5172413793103449, 3.868794716113063, 1.4146026704452719, 'UPHENO:0002844', 'abnormal head'),
(415761, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0100321', 'abnormal eye muscle', 0.5294117647058824, 5.968280811662945, 1.7775483331720507, 'UPHENO:0002816', 'abnormal musculature'),
(415762, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0101177', 'abnormal m. obliquus superior', 0.5142857142857142, 5.968280811662945, 1.7519707646772533, 'UPHENO:0002816', 'abnormal musculature'),
(415763, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0100422', 'abnormal notochord', 0.42857142857142855, 3.9037819259951223, 1.293464107292913, 'HP:0033127', 'Abnormality of the musculoskeletal system'),
(415764, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0100481', 'abnormal anatomical line', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(415765, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0100688', 'abnormal adipose tissue', 0.42857142857142855, 3.9037819259951223, 1.293464107292913, 'HP:0033127', 'Abnormality of the musculoskeletal system'),
(415766, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0101261', 'abnormal m. dilatator laryngis', 0.5142857142857142, 5.968280811662945, 1.7519707646772533, 'UPHENO:0002816', 'abnormal musculature'),
(415767, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0100026', 'abnormal germ cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(415768, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0100591', 'abnormal pharyngeal arch', 0.45454545454545453, 3.868794716113063, 1.3261006948111689, 'UPHENO:0002844', 'abnormal head'),
(415769, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0101326', 'abnormal cementoblast', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(415770, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0131672', 'abnormal non-neurogenic ectodermal placode', 0.46875, 3.868794716113063, 1.346661621632546, 'UPHENO:0002844', 'abnormal head'),
(415771, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0131666', 'abnormal adherens junction', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(415772, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0101018', 'abnormal m. rectus inferior', 0.5142857142857142, 5.968280811662945, 1.7519707646772533, 'UPHENO:0002816', 'abnormal musculature'),
(415773, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0100661', 'abnormal gill primordium', 0.4166666666666667, 3.868794716113063, 1.2696447528267278, 'UPHENO:0002844', 'abnormal head'),
(415774, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0101513', 'abnormal basal body', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(415775, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0101071', 'abnormal endoplasmic reticulum', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(415776, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0101373', 'abnormal oxygen accumulating cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(415777, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0101569', 'abnormal activin-induced ectoderm', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(415778, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0100479', 'abnormal lens placode', 0.4166666666666667, 3.868794716113063, 1.2696447528267278, 'UPHENO:0002844', 'abnormal head'),
(415779, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0101522', 'abnormal m. rectus posterior', 0.5142857142857142, 5.968280811662945, 1.7519707646772533, 'UPHENO:0002816', 'abnormal musculature'),
(415780, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0101060', 'abnormal m. rectus superior', 0.5142857142857142, 5.968280811662945, 1.7519707646772533, 'UPHENO:0002816', 'abnormal musculature'),
(415781, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0100417', 'abnormal dense regular connective tissue', 0.42857142857142855, 3.9037819259951223, 1.293464107292913, 'HP:0033127', 'Abnormality of the musculoskeletal system'),
(415782, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0100626', 'abnormal primordial germ cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(415783, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0142052', 'abnormal nasal region', 0.5769230769230769, 3.868794716113063, 1.493986931537117, 'UPHENO:0002844', 'abnormal head'),
(415784, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0100894', 'abnormal nucleus', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(415785, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0107284', 'abnormal migrating myoblast', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(415786, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0101379', 'abnormal mm. constrictores branchiales II', 0.5142857142857142, 5.968280811662945, 1.7519707646772533, 'UPHENO:0002816', 'abnormal musculature'),
(415787, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0100948', 'abnormal m. petrohyoideus', 0.5294117647058824, 5.968280811662945, 1.7775483331720507, 'UPHENO:0002816', 'abnormal musculature'),
(415788, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0100381', 'abnormal mandibular head muscle', 0.5294117647058824, 5.968280811662945, 1.7775483331720507, 'UPHENO:0002816', 'abnormal musculature'),
(415789, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0101174', 'abnormal articular system', 0.41379310344827586, 3.9037819259951223, 1.270967363209146, 'HP:0033127', 'Abnormality of the musculoskeletal system'),
(415790, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0100664', 'abnormal periocular region', 0.5357142857142857, 3.868794716113063, 1.4396418297332543, 'UPHENO:0002844', 'abnormal head'),
(415791, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0100451', 'abnormal head mesenchyme', 0.5172413793103449, 3.868794716113063, 1.4146026704452719, 'UPHENO:0002844', 'abnormal head'),
(415792, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0100852', 'abnormal interdigital region', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(415793, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0100754', 'abnormal electrically active cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(415794, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0100374', 'abnormal pharyngeal endoderm', 0.45454545454545453, 3.868794716113063, 1.3261006948111689, 'UPHENO:0002844', 'abnormal head'),
(415795, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0126353', 'abnormally localised cranial muscle', 0.4090909090909091, 5.968280811662945, 1.562552214472535, 'UPHENO:0002816', 'abnormal musculature'),
(415796, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0100791', 'abnormal multiciliated cell precursor', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(415797, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0100653', 'abnormal myoblast', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(415798, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0141839', 'edematous pharyngeal region', 0.40540540540540543, 3.868794716113063, 1.2523698696136485, 'UPHENO:0002844', 'abnormal head'),
(415799, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0100247', 'abnormal cranial ganglion', 0.40540540540540543, 3.868794716113063, 1.2523698696136485, 'UPHENO:0002844', 'abnormal head'),
(415800, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0100774', 'abnormal m. levator mandibulae articularis', 0.5142857142857142, 5.968280811662945, 1.7519707646772533, 'UPHENO:0002816', 'abnormal musculature'),
(415801, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0100337', 'abnormal zygote', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(415802, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0127915', 'abnormally localised lateral nasal prominence', 0.40540540540540543, 3.868794716113063, 1.2523698696136485, 'UPHENO:0002844', 'abnormal head'),
(415803, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0142025', 'abnormally localised nasal region', 0.40540540540540543, 3.868794716113063, 1.2523698696136485, 'UPHENO:0002844', 'abnormal head'),
(415804, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0100373', 'abnormal splanchnocranium', 0.45714285714285713, 3.9037819259951223, 1.3358839857233322, 'HP:0033127', 'Abnormality of the musculoskeletal system'),
(415805, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0101324', 'abnormal m. transversus anterior', 0.5142857142857142, 5.968280811662945, 1.7519707646772533, 'UPHENO:0002816', 'abnormal musculature'),
(415806, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0100049', 'abnormal chondrocranium', 0.45714285714285713, 3.9037819259951223, 1.3358839857233322, 'HP:0033127', 'Abnormality of the musculoskeletal system'),
(415807, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0100465', 'abnormal skeletal system', 0.42857142857142855, 3.9037819259951223, 1.293464107292913, 'HP:0033127', 'Abnormality of the musculoskeletal system'),
(415808, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0100708', 'abnormal laryngeal muscle', 0.5294117647058824, 5.968280811662945, 1.7775483331720507, 'UPHENO:0002816', 'abnormal musculature'),
(415809, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0100161', 'abnormal hindbrain', 0.40540540540540543, 3.868794716113063, 1.2523698696136485, 'UPHENO:0002844', 'abnormal head'),
(415810, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0100638', 'abnormal polar body', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(415811, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0100100', 'abnormal muscle', 0.4827586206896552, 5.968280811662945, 1.6974212831607063, 'UPHENO:0002816', 'abnormal musculature'),
(415812, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0100813', 'abnormal branchial arch 3', 0.42857142857142855, 3.868794716113063, 1.2876547978142938, 'UPHENO:0002844', 'abnormal head'),
(415813, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0100317', 'abnormal respiratory system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(415814, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0101108', 'abnormal hypobranchial head muscle', 0.5294117647058824, 5.968280811662945, 1.7775483331720507, 'UPHENO:0002816', 'abnormal musculature'),
(415815, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0100592', 'abnormal auditory apparatus', 0.4166666666666667, 3.868794716113063, 1.2696447528267278, 'UPHENO:0002844', 'abnormal head'),
(415816, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0101404', 'abnormal m. interhyoideus', 0.5142857142857142, 5.968280811662945, 1.7519707646772533, 'UPHENO:0002816', 'abnormal musculature'),
(415817, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0101144', 'abnormal fenestra subocularis', 0.43243243243243246, 3.9037819259951223, 1.2992774584144207, 'HP:0033127', 'Abnormality of the musculoskeletal system'),
(415818, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0100880', 'abnormal head mesoderm', 0.45454545454545453, 3.868794716113063, 1.3261006948111689, 'UPHENO:0002844', 'abnormal head'),
(415819, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0115526', 'abnormally incomplete structure of head', 0.40540540540540543, 3.868794716113063, 1.2523698696136485, 'UPHENO:0002844', 'abnormal head'),
(415820, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0103843', 'abnormally localised head', 0.42857142857142855, 3.868794716113063, 1.2876547978142938, 'UPHENO:0002844', 'abnormal head'),
(415821, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0101547', 'abnormal lampbrush chromosome', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(415822, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0100907', 'abnormal cytoplasm', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(415823, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0101164', 'abnormal m. cucullaris', 0.5294117647058824, 5.968280811662945, 1.7775483331720507, 'UPHENO:0002816', 'abnormal musculature'),
(415824, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0107285', 'abnormal flexural organ', 0.41379310344827586, 3.9037819259951223, 1.270967363209146, 'HP:0033127', 'Abnormality of the musculoskeletal system'),
(415825, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0100372', 'abnormal hematological system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(415826, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0142059', 'abnormal nasal region morphology', 0.40540540540540543, 3.868794716113063, 1.2523698696136485, 'UPHENO:0002844', 'abnormal head'),
(415827, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0101551', 'abnormal m. levator mandibulae longus internus', 0.5142857142857142, 5.968280811662945, 1.7519707646772533, 'UPHENO:0002816', 'abnormal musculature'),
(415828, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0100477', 'abnormal pericyte', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(415829, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0141714', 'abnormal anterior notochord', 0.41379310344827586, 3.9037819259951223, 1.270967363209146, 'HP:0033127', 'Abnormality of the musculoskeletal system'),
(415830, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0100640', 'abnormal notochordal sheath', 0.41379310344827586, 3.9037819259951223, 1.270967363209146, 'HP:0033127', 'Abnormality of the musculoskeletal system'),
(415831, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0100006', 'abnormal anatomical structure', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(415832, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0101469', 'abnormal medial nasal prominence', 0.5172413793103449, 3.868794716113063, 1.4146026704452719, 'UPHENO:0002844', 'abnormal head'),
(415833, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0101138', 'abnormal m. rectus cervicus', 0.5142857142857142, 5.968280811662945, 1.7519707646772533, 'UPHENO:0002816', 'abnormal musculature'),
(415834, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0107258', 'abnormal anatomical axis', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(415835, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0100460', 'abnormal ethmoid region', 0.45714285714285713, 3.9037819259951223, 1.3358839857233322, 'HP:0033127', 'Abnormality of the musculoskeletal system'),
(415836, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0100969', 'abnormal disaggregated/reaggregated ectoderm treated with activin', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(415837, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0100583', 'abnormal mandibular arch skeleton', 0.42105263157894735, 3.9037819259951223, 1.282067725609914, 'HP:0033127', 'Abnormality of the musculoskeletal system'),
(415838, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0127512', 'abnormally localised medial nasal prominence', 0.40540540540540543, 3.868794716113063, 1.2523698696136485, 'UPHENO:0002844', 'abnormal head'),
(415839, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0100724', 'abnormal kinetochore', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(415840, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0100687', 'abnormal periotic region', 0.5357142857142857, 3.868794716113063, 1.4396418297332543, 'UPHENO:0002844', 'abnormal head'),
(415841, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0101418', 'abnormal m. levator scapulae superior', 0.5294117647058824, 5.968280811662945, 1.7775483331720507, 'UPHENO:0002816', 'abnormal musculature'),
(415842, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0100340', 'abnormal midbrain', 0.40540540540540543, 3.868794716113063, 1.2523698696136485, 'UPHENO:0002844', 'abnormal head'),
(415843, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0101237', 'abnormal mucus secreting cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(415844, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0100893', 'abnormal hyoid arch', 0.4411764705882353, 3.868794716113063, 1.306453672460365, 'UPHENO:0002844', 'abnormal head'),
(415845, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0131678', 'abnormal intercanthal region', 0.5, 3.868794716113063, 1.3908261422825396, 'UPHENO:0002844', 'abnormal head'),
(415846, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0101535', 'abnormal absorptive cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(415847, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0100940', 'abnormal hatching gland primordium', 0.5, 3.868794716113063, 1.3908261422825396, 'UPHENO:0002844', 'abnormal head'),
(415848, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0107312', 'abnormal filopodium', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(415849, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0101196', 'abnormal occipital region', 0.45714285714285713, 3.9037819259951223, 1.3358839857233322, 'HP:0033127', 'Abnormality of the musculoskeletal system'),
(415850, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0101240', 'abnormal ciliated non-epidermal cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(415851, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0126822', 'abnormally localised pharyngeal region', 0.4411764705882353, 3.868794716113063, 1.306453672460365, 'UPHENO:0002844', 'abnormal head'),
(415852, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0100308', 'abnormal early embryonic cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(415853, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0101455', 'abnormal m. orbitohyoideus', 0.5142857142857142, 5.968280811662945, 1.7519707646772533, 'UPHENO:0002816', 'abnormal musculature'),
(415854, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0101132', 'abnormal apoptotic cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(415855, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0100359', 'abnormal trigeminal placode', 0.4411764705882353, 3.868794716113063, 1.306453672460365, 'UPHENO:0002844', 'abnormal head'),
(415856, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0100691', 'abnormal keratin accumulating cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(415857, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0141718', 'abnormal posterior notochord', 0.41379310344827586, 3.9037819259951223, 1.270967363209146, 'HP:0033127', 'Abnormality of the musculoskeletal system'),
(415858, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0101544', 'abnormal fenestra basicranialis', 0.43243243243243246, 3.9037819259951223, 1.2992774584144207, 'HP:0033127', 'Abnormality of the musculoskeletal system'),
(415859, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0101241', 'abnormal nucleate erythrocyte', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(415860, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0101061', 'abnormal plasma membrane', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(415861, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0101088', 'abnormal dermatocranium', 0.45714285714285713, 3.9037819259951223, 1.3358839857233322, 'HP:0033127', 'Abnormality of the musculoskeletal system'),
(415862, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0100932', 'abnormal olfactory region', 0.45714285714285713, 3.9037819259951223, 1.3358839857233322, 'HP:0033127', 'Abnormality of the musculoskeletal system'),
(415863, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0101447', 'abnormal m. quadrato-hyoangularis', 0.5142857142857142, 5.968280811662945, 1.7519707646772533, 'UPHENO:0002816', 'abnormal musculature'),
(415864, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0100798', 'abnormal mm. levator arcuum branchialium I', 0.5142857142857142, 5.968280811662945, 1.7519707646772533, 'UPHENO:0002816', 'abnormal musculature'),
(415865, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0100802', 'abnormal exocrine cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(415866, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0100078', 'abnormal neurogenic placode', 0.46875, 3.868794716113063, 1.346661621632546, 'UPHENO:0002844', 'abnormal head'),
(415867, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0100172', 'abnormal stem cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(415868, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0100002', 'abnormal head', 0.5769230769230769, 3.868794716113063, 1.493986931537117, 'UPHENO:0002844', 'abnormal head'),
(415869, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0100004', 'abnormal cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(415870, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0100906', 'abnormal lateral nasal prominence', 0.5172413793103449, 3.868794716113063, 1.4146026704452719, 'UPHENO:0002844', 'abnormal head'),
(415871, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0102259', 'abnormal pharyngeal region morphology', 0.42857142857142855, 3.868794716113063, 1.2876547978142938, 'UPHENO:0002844', 'abnormal head'),
(415872, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0101256', 'abnormal head endoderm', 0.46875, 3.868794716113063, 1.346661621632546, 'UPHENO:0002844', 'abnormal head'),
(415873, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0100956', 'abnormal centrosome', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(415874, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0100365', 'abnormal braincase and otic capsule skeleton', 0.43243243243243246, 3.9037819259951223, 1.2992774584144207, 'HP:0033127', 'Abnormality of the musculoskeletal system'),
(415875, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0100132', 'abnormal cranium', 0.47058823529411764, 3.9037819259951223, 1.3553869733500896, 'HP:0033127', 'Abnormality of the musculoskeletal system'),
(415876, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0100715', 'abnormal ciliated cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(415877, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0100081', 'abnormal anatomical entity in vitro', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(415878, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0100289', 'abnormal chondroblast', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(415879, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0101540', 'abnormal m. rectus anterior', 0.5142857142857142, 5.968280811662945, 1.7519707646772533, 'UPHENO:0002816', 'abnormal musculature'),
(415880, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0100388', 'abnormal adenohypophyseal placode', 0.4411764705882353, 3.868794716113063, 1.306453672460365, 'UPHENO:0002844', 'abnormal head'),
(415881, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0100169', 'abnormal brain', 0.4166666666666667, 3.868794716113063, 1.2696447528267278, 'UPHENO:0002844', 'abnormal head'),
(415882, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0100496', 'abnormal hyoid head muscle', 0.5294117647058824, 5.968280811662945, 1.7775483331720507, 'UPHENO:0002816', 'abnormal musculature'),
(415883, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0100727', 'abnormal odontogenic papilla', 0.5555555555555556, 3.868794716113063, 1.4660594796394144, 'UPHENO:0002844', 'abnormal head'),
(415884, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0100746', 'abnormal smooth muscle', 0.4666666666666667, 5.968280811662945, 1.6688911624516964, 'UPHENO:0002816', 'abnormal musculature'),
(415885, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0100678', 'abnormal m. levator scapulae inferior', 0.5294117647058824, 5.968280811662945, 1.7775483331720507, 'UPHENO:0002816', 'abnormal musculature'),
(415886, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0101276', 'abnormal mm. levator arcuum branchialium IV', 0.5142857142857142, 5.968280811662945, 1.7519707646772533, 'UPHENO:0002816', 'abnormal musculature'),
(415887, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0100976', 'abnormal multiciliated cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(415888, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0101264', 'abnormal mitotic spindle', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(415889, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0100571', 'abnormal branchial arch 1', 0.42857142857142855, 3.868794716113063, 1.2876547978142938, 'UPHENO:0002844', 'abnormal head'),
(415890, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0101228', 'abnormal mesenchymal stem cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(415891, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0100572', 'abnormal branchial arch', 0.4411764705882353, 3.868794716113063, 1.306453672460365, 'UPHENO:0002844', 'abnormal head'),
(415892, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0100627', 'abnormal pharyngeal region', 0.5555555555555556, 3.868794716113063, 1.4660594796394144, 'UPHENO:0002844', 'abnormal head'),
(415893, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0100546', 'abnormal whole organism', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(415894, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0101289', 'abnormal orbital region', 0.41025641025641024, 3.9037819259951223, 1.2655242231512656, 'HP:0033127', 'Abnormality of the musculoskeletal system'),
(415895, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0131667', 'abnormal actin cytoskeleton', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(415896, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0142057', 'abnormal desmosome', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(415897, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0101297', 'abnormal barrier cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(415898, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0101333', 'abnormal barrier epithelial cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(415899, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0100704', 'abnormal Merkel cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(415900, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0100232', 'abnormal lymphatic system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(415901, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0100596', 'abnormal myocyte', 0.42424242424242425, 5.968280811662945, 1.591225288920281, 'UPHENO:0002816', 'abnormal musculature'),
(415902, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0126449', 'abnormally localised head region', 0.42857142857142855, 3.868794716113063, 1.2876547978142938, 'UPHENO:0002844', 'abnormal head'),
(415903, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0101290', 'abnormal mm. levator arcuum branchialium III', 0.5142857142857142, 5.968280811662945, 1.7519707646772533, 'UPHENO:0002816', 'abnormal musculature'),
(415904, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0100437', 'abnormal proepicardium', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(415905, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0100450', 'abnormal circumpharyngeal ridge', 0.5, 3.868794716113063, 1.3908261422825396, 'UPHENO:0002844', 'abnormal head'),
(415906, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0100380', 'abnormal m. levator mandibulae longus superficialis', 0.5142857142857142, 5.968280811662945, 1.7519707646772533, 'UPHENO:0002816', 'abnormal musculature'),
(415907, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0100515', 'abnormal somatic stem cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(415908, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0100879', 'abnormal m. depressor mandibulae', 0.5294117647058824, 5.968280811662945, 1.7775483331720507, 'UPHENO:0002816', 'abnormal musculature'),
(415909, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0100549', 'abnormal mitotic cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(415910, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0100629', 'abnormal branchial arch 2', 0.42857142857142855, 3.868794716113063, 1.2876547978142938, 'UPHENO:0002844', 'abnormal head'),
(415911, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0100344', 'abnormal portion of organism substance', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(415912, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0100977', 'abnormal m. obliquus inferior', 0.5142857142857142, 5.968280811662945, 1.7519707646772533, 'UPHENO:0002816', 'abnormal musculature'),
(415913, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0125199', 'absent pharyngeal region', 0.4166666666666667, 3.868794716113063, 1.2696447528267278, 'UPHENO:0002844', 'abnormal head'),
(415914, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0101520', 'abnormal otic region', 0.45714285714285713, 3.9037819259951223, 1.3358839857233322, 'HP:0033127', 'Abnormality of the musculoskeletal system'),
(415915, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0101334', 'abnormal olfactory pit', 0.42857142857142855, 3.868794716113063, 1.2876547978142938, 'UPHENO:0002844', 'abnormal head'),
(415916, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0100721', 'abnormal centromere', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(415917, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0131562', 'abnormally localised intercanthal region', 0.40540540540540543, 3.868794716113063, 1.2523698696136485, 'UPHENO:0002844', 'abnormal head'),
(415918, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0100928', 'abnormal m. levator mandibulae externus', 0.5142857142857142, 5.968280811662945, 1.7519707646772533, 'UPHENO:0002816', 'abnormal musculature'),
(415919, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0100463', 'abnormal m. transversus ventralis II', 0.5142857142857142, 5.968280811662945, 1.7519707646772533, 'UPHENO:0002816', 'abnormal musculature'),
(415920, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0100719', 'abnormal sphenoid region', 0.45714285714285713, 3.9037819259951223, 1.3358839857233322, 'HP:0033127', 'Abnormality of the musculoskeletal system'),
(415921, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0101004', 'abnormal acid secreting cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(415922, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0115812', 'duplicated head', 0.4411764705882353, 3.868794716113063, 1.306453672460365, 'UPHENO:0002844', 'abnormal head'),
(415923, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0100899', 'abnormal secondary spermatogonium', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(415924, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0100888', 'abnormal microtubule', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(415925, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0100108', 'abnormal cell part', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(415926, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0100788', 'abnormal branchial arch 4', 0.42857142857142855, 3.868794716113063, 1.2876547978142938, 'UPHENO:0002844', 'abnormal head'),
(415927, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0101581', 'abnormal mm. constrictores branchiales III', 0.5142857142857142, 5.968280811662945, 1.7519707646772533, 'UPHENO:0002816', 'abnormal musculature'),
(415928, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0100225', 'abnormal endocrine system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(415929, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0100429', 'abnormal spermatid', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(415930, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0101153', 'abnormal musculature of face', 0.42857142857142855, 5.968280811662945, 1.5993231798388445, 'UPHENO:0002816', 'abnormal musculature'),
(415931, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0100730', 'abnormal m. subarcualis rectus I', 0.5142857142857142, 5.968280811662945, 1.7519707646772533, 'UPHENO:0002816', 'abnormal musculature'),
(415932, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0101435', 'abnormal paracrine cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(415933, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0124840', 'absent head region', 0.40540540540540543, 3.868794716113063, 1.2523698696136485, 'UPHENO:0002844', 'abnormal head'),
(415934, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0101481', 'abnormal skeletal muscle satellite cell', 0.4117647058823529, 5.968280811662945, 1.5676502776568768, 'UPHENO:0002816', 'abnormal musculature'),
(415935, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0100594', 'abnormal Jacobsons organ', 0.4166666666666667, 3.868794716113063, 1.2696447528267278, 'UPHENO:0002844', 'abnormal head'),
(415936, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0100769', 'abnormal neurocranium', 0.45714285714285713, 3.9037819259951223, 1.3358839857233322, 'HP:0033127', 'Abnormality of the musculoskeletal system'),
(415937, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0101102', 'abnormal craniofacial region', 0.5172413793103449, 3.868794716113063, 1.4146026704452719, 'UPHENO:0002844', 'abnormal head'),
(415938, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0100025', 'abnormal oocyte', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(415939, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0100052', 'abnormal head somite', 0.40540540540540543, 3.868794716113063, 1.2523698696136485, 'UPHENO:0002844', 'abnormal head'),
(415940, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0100533', 'abnormal melanoblast', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(415941, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0100501', 'abnormal urogenital system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(415942, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0101357', 'abnormal m. intermandibularis', 0.5142857142857142, 5.968280811662945, 1.7519707646772533, 'UPHENO:0002816', 'abnormal musculature'),
(415943, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0100285', 'abnormal progenitor cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(415944, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0101001', 'abnormal ventricular zone', 0.40540540540540543, 3.868794716113063, 1.2523698696136485, 'UPHENO:0002844', 'abnormal head'),
(415945, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0100275', 'abnormal skeletal muscle', 0.4666666666666667, 5.968280811662945, 1.6688911624516964, 'UPHENO:0002816', 'abnormal musculature'),
(415946, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0101178', 'abnormal m. levator mandibulae longus profundus', 0.5142857142857142, 5.968280811662945, 1.7519707646772533, 'UPHENO:0002816', 'abnormal musculature'),
(415947, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0100902', 'abnormal spermatocyte', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(415948, 'HP:0040172', 'Abnormality of occipitofrontalis muscle', 'XPO:0100740', 'abnormal profundal placode', 0.45454545454545453, 3.868794716113063, 1.3261006948111689, 'UPHENO:0002844', 'abnormal head'),
(415949, 'HP:0100139', 'Fragmentation of the epiphysis of the distal phalanx of the 3rd toe', 'XPO:0102566', 'abnormal claw primordium morphology', 0.40186915887850466, 7.639349617137506, 1.752146970153439, 'UPHENO:0088132', 'abnormal pedal digit morphology'),
(415950, 'HP:0030865', 'Large elbow', 'XPO:0100970', 'abnormal carpus', 0.4696969696969697, 9.696350005340756, 2.1340914260241406, 'HP:0009810', 'Abnormality of upper limb joint'),
(415951, 'HP:0030865', 'Large elbow', 'XPO:0102400', 'abnormal pectoral girdle morphology', 0.40625, 6.7562089344983995, 1.6567165960537653, 'UPHENO:0079876', 'abnormal anatomical entity morphology in the pectoral complex'),
(415952, 'HP:0030865', 'Large elbow', 'XPO:0103218', 'abnormal joint morphology', 0.46, 9.103525386846629, 2.046367923407091, 'UPHENO:0016527', 'abnormal skeletal joint morphology in the independent continuant'),
(415953, 'HP:0030865', 'Large elbow', 'XPO:0102806', 'abnormal articular system morphology', 0.43478260869565216, 4.638757693672553, 1.4201588541997616, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(415954, 'HP:0030865', 'Large elbow', 'XPO:0102010', 'abnormal perichondrium morphology', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(415955, 'HP:0030865', 'Large elbow', 'XPO:0107372', 'abnormal flexural organ morphology', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(415956, 'HP:0030865', 'Large elbow', 'XPO:0141719', 'abnormal anterior notochord morphology', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(415957, 'HP:0030865', 'Large elbow', 'XPO:0140565', 'abnormally necrotic joint', 0.41818181818181815, 9.103525386846629, 1.9511352588008508, 'UPHENO:0016527', 'abnormal skeletal joint morphology in the independent continuant'),
(415958, 'HP:0030865', 'Large elbow', 'XPO:0102054', 'abnormal notochord morphology', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(415959, 'HP:0030865', 'Large elbow', 'XPO:0141723', 'abnormal posterior notochord morphology', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(415960, 'HP:0030865', 'Large elbow', 'XPO:0102567', 'abnormal skeleton morphology', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(415961, 'HP:0030865', 'Large elbow', 'XPO:0102484', 'abnormal interdigital region morphology', 0.4090909090909091, 5.914846961127896, 1.5555417450076394, 'UPHENO:0084763', 'abnormal anatomical entity morphology in the appendage girdle complex'),
(415962, 'HP:0030865', 'Large elbow', 'XPO:0129427', 'decreased size of the joint', 0.40350877192982454, 9.103525386846629, 1.9165991623389758, 'UPHENO:0016527', 'abnormal skeletal joint morphology in the independent continuant'),
(415963, 'HP:0030865', 'Large elbow', 'XPO:0101860', 'abnormal skeletal subdivision morphology', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(415964, 'HP:0030865', 'Large elbow', 'XPO:0102217', 'abnormal elastica externa morphology', 0.4444444444444444, 4.638757693672553, 1.4358516936218344, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(415965, 'HP:0030865', 'Large elbow', 'XPO:0102272', 'abnormal notochordal sheath morphology', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(415966, 'HP:0030865', 'Large elbow', 'XPO:0102097', 'abnormal skeletal system morphology', 0.4444444444444444, 4.638757693672553, 1.4358516936218344, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(415967, 'HP:0025321', 'Copper accumulation in liver', 'XPO:0103168', 'abnormal liver parenchyme morphology', 0.4375, 10.01729298920255, 2.0934578292328023, 'UPHENO:0019492', 'abnormal liver morphology'),
(415968, 'HP:0025321', 'Copper accumulation in liver', 'XPO:0141647', 'neoplastic liver', 0.42168674698795183, 10.01729298920255, 2.0552760627813575, 'UPHENO:0019492', 'abnormal liver morphology'),
(415969, 'HP:0025321', 'Copper accumulation in liver', 'XPO:0127068', 'abnormally localised hepatic vein', 0.40229885057471265, 10.01729298920255, 2.0074724046487695, 'UPHENO:0019492', 'abnormal liver morphology'),
(415970, 'HP:0025321', 'Copper accumulation in liver', 'XPO:0130724', 'increased size of the liver parenchyme', 0.40229885057471265, 10.01729298920255, 2.0074724046487695, 'UPHENO:0019492', 'abnormal liver morphology'),
(415971, 'HP:0025321', 'Copper accumulation in liver', 'XPO:0102426', 'abnormal liver morphology', 0.4375, 10.01729298920255, 2.0934578292328023, 'UPHENO:0019492', 'abnormal liver morphology'),
(415972, 'HP:0025321', 'Copper accumulation in liver', 'XPO:0129248', 'decreased size of the liver parenchyme', 0.40229885057471265, 10.01729298920255, 2.0074724046487695, 'UPHENO:0019492', 'abnormal liver morphology'),
(415973, 'HP:0025321', 'Copper accumulation in liver', 'XPO:0100042', 'abnormal hepatic vein', 0.45454545454545453, 10.01729298920255, 2.133849806123212, 'UPHENO:0019492', 'abnormal liver morphology'),
(415974, 'HP:0025321', 'Copper accumulation in liver', 'XPO:0141125', 'abnormally necrotic liver parenchyme', 0.4117647058823529, 10.01729298920255, 2.0309524124007297, 'UPHENO:0019492', 'abnormal liver morphology'),
(415975, 'HP:0000890', 'Long clavicles', 'XPO:0128619', 'decreased size of the pectoral girdle', 0.449438202247191, 10.335532897059798, 2.1552687360329936, 'UPHENO:0002982', 'abnormal pectoral girdle region'),
(415976, 'HP:0000890', 'Long clavicles', 'XPO:0102865', 'abnormal scapula morphology', 0.42990654205607476, 10.335532897059798, 2.107916793443655, 'UPHENO:0002982', 'abnormal pectoral girdle region'),
(415977, 'HP:0000890', 'Long clavicles', 'XPO:0130099', 'increased size of the pectoral girdle', 0.4883720930232558, 10.335532897059798, 2.246683296205277, 'UPHENO:0002982', 'abnormal pectoral girdle region'),
(415978, 'HP:0000890', 'Long clavicles', 'XPO:0102383', 'abnormal coracoid bone morphology', 0.42990654205607476, 10.335532897059798, 2.107916793443655, 'UPHENO:0002982', 'abnormal pectoral girdle region'),
(415979, 'HP:0000890', 'Long clavicles', 'XPO:0102400', 'abnormal pectoral girdle morphology', 0.48148148148148145, 10.335532897059798, 2.2307773737369985, 'UPHENO:0002982', 'abnormal pectoral girdle region'),
(415980, 'HP:0000890', 'Long clavicles', 'XPO:0130894', 'increased size of the coracoid bone', 0.4049586776859504, 10.335532897059798, 2.045840593783635, 'UPHENO:0002982', 'abnormal pectoral girdle region'),
(415981, 'HP:0000890', 'Long clavicles', 'XPO:0140731', 'abnormally necrotic pectoral girdle', 0.4482758620689655, 10.335532897059798, 2.152479946334375, 'UPHENO:0002982', 'abnormal pectoral girdle region'),
(415982, 'HP:0000890', 'Long clavicles', 'XPO:0130676', 'increased size of the scapula', 0.4049586776859504, 10.335532897059798, 2.045840593783635, 'UPHENO:0002982', 'abnormal pectoral girdle region'),
(415983, 'HP:0032807', 'Neonatal seizure', 'XPO:0100358', 'abnormal ganglion', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(415984, 'HP:0032807', 'Neonatal seizure', 'XPO:0100954', 'abnormal neural progenitor cell', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(415985, 'HP:0032807', 'Neonatal seizure', 'XPO:0100704', 'abnormal Merkel cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(415986, 'HP:0032807', 'Neonatal seizure', 'XPO:0100537', 'abnormal medium cavity', 0.43333333333333335, 3.94131651835137, 1.3068679445984308, 'UPHENO:0004523', 'abnormal nervous system'),
(415987, 'HP:0032807', 'Neonatal seizure', 'XPO:0100587', 'abnormal vestibuloauditory system', 0.4642857142857143, 3.94131651835137, 1.3527368387638634, 'UPHENO:0004523', 'abnormal nervous system'),
(415988, 'HP:0032807', 'Neonatal seizure', 'XPO:0100274', 'abnormal sensory system', 0.48148148148148145, 3.94131651835137, 1.3775597686645948, 'UPHENO:0004523', 'abnormal nervous system'),
(415989, 'HP:0032807', 'Neonatal seizure', 'XPO:0100760', 'abnormal Stirnorgan', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(415990, 'HP:0032807', 'Neonatal seizure', 'XPO:0101297', 'abnormal barrier cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(415991, 'HP:0032807', 'Neonatal seizure', 'XPO:0100702', 'abnormal glial cell', 0.43333333333333335, 3.94131651835137, 1.3068679445984308, 'UPHENO:0004523', 'abnormal nervous system'),
(415992, 'HP:0032807', 'Neonatal seizure', 'XPO:0100337', 'abnormal zygote', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(415993, 'HP:0032807', 'Neonatal seizure', 'XPO:0107253', 'abnormal enteric nervous system', 0.48148148148148145, 3.94131651835137, 1.3775597686645948, 'UPHENO:0004523', 'abnormal nervous system'),
(415994, 'HP:0032807', 'Neonatal seizure', 'XPO:0100026', 'abnormal germ cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(415995, 'HP:0032807', 'Neonatal seizure', 'XPO:0100172', 'abnormal stem cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(415996, 'HP:0032807', 'Neonatal seizure', 'XPO:0101535', 'abnormal absorptive cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(415997, 'HP:0032807', 'Neonatal seizure', 'XPO:0100802', 'abnormal exocrine cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(415998, 'HP:0032807', 'Neonatal seizure', 'XPO:0100715', 'abnormal ciliated cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(415999, 'HP:0032807', 'Neonatal seizure', 'XPO:0100734', 'abnormal lateral line system', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(416000, 'HP:0032807', 'Neonatal seizure', 'XPO:0100108', 'abnormal cell part', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(416001, 'HP:0032807', 'Neonatal seizure', 'XPO:0100642', 'abnormal gustatory system', 0.4642857142857143, 3.94131651835137, 1.3527368387638634, 'UPHENO:0004523', 'abnormal nervous system'),
(416002, 'HP:0032807', 'Neonatal seizure', 'XPO:0100289', 'abnormal chondroblast', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(416003, 'HP:0032807', 'Neonatal seizure', 'XPO:0100858', 'abnormal presumptive midbrain-hindbrain boundary', 0.43333333333333335, 3.94131651835137, 1.3068679445984308, 'UPHENO:0004523', 'abnormal nervous system'),
(416004, 'HP:0032807', 'Neonatal seizure', 'XPO:0101326', 'abnormal cementoblast', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(416005, 'HP:0032807', 'Neonatal seizure', 'XPO:0101373', 'abnormal oxygen accumulating cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(416006, 'HP:0032807', 'Neonatal seizure', 'XPO:0100004', 'abnormal cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(416007, 'HP:0032807', 'Neonatal seizure', 'XPO:0101237', 'abnormal mucus secreting cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(416008, 'HP:0032807', 'Neonatal seizure', 'XPO:0100031', 'abnormal central nervous system', 0.48148148148148145, 3.94131651835137, 1.3775597686645948, 'UPHENO:0004523', 'abnormal nervous system'),
(416009, 'HP:0032807', 'Neonatal seizure', 'XPO:0100196', 'abnormal neuron', 0.43333333333333335, 3.94131651835137, 1.3068679445984308, 'UPHENO:0004523', 'abnormal nervous system'),
(416010, 'HP:0032807', 'Neonatal seizure', 'XPO:0100533', 'abnormal melanoblast', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(416011, 'HP:0032807', 'Neonatal seizure', 'XPO:0100032', 'abnormal nervous system', 0.5, 3.94131651835137, 1.4038013602984167, 'UPHENO:0004523', 'abnormal nervous system'),
(416012, 'HP:0032807', 'Neonatal seizure', 'XPO:0100285', 'abnormal progenitor cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(416013, 'HP:0032807', 'Neonatal seizure', 'XPO:0142051', 'abnormal cerebrospinal fluid', 0.4482758620689655, 3.94131651835137, 1.3292091859262085, 'UPHENO:0004523', 'abnormal nervous system'),
(416014, 'HP:0032807', 'Neonatal seizure', 'XPO:0131654', 'abnormal neuron projection', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(416015, 'HP:0032807', 'Neonatal seizure', 'XPO:0100638', 'abnormal polar body', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(416016, 'HP:0032807', 'Neonatal seizure', 'XPO:0107287', 'abnormal afferent neuron', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(416017, 'HP:0032807', 'Neonatal seizure', 'XPO:0100336', 'abnormal interneuron', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(416018, 'HP:0032807', 'Neonatal seizure', 'XPO:0100175', 'abnormal migrating neuroblast', 0.43333333333333335, 3.94131651835137, 1.3068679445984308, 'UPHENO:0004523', 'abnormal nervous system'),
(416019, 'HP:0032807', 'Neonatal seizure', 'XPO:0100549', 'abnormal mitotic cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(416020, 'HP:0032807', 'Neonatal seizure', 'XPO:0107286', 'abnormal efferent neuron', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(416021, 'HP:0032807', 'Neonatal seizure', 'XPO:0100791', 'abnormal multiciliated cell precursor', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(416022, 'HP:0032807', 'Neonatal seizure', 'XPO:0100864', 'abnormal dorsolateral ascending neuron', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(416023, 'HP:0032807', 'Neonatal seizure', 'XPO:0100344', 'abnormal portion of organism substance', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416024, 'HP:0032807', 'Neonatal seizure', 'XPO:0100754', 'abnormal electrically active cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(416025, 'HP:0032807', 'Neonatal seizure', 'XPO:0101448', 'abnormal myelin accumulating cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(416026, 'HP:0032807', 'Neonatal seizure', 'XPO:0100852', 'abnormal interdigital region', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(416027, 'HP:0032807', 'Neonatal seizure', 'XPO:0100477', 'abnormal pericyte', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(416028, 'HP:0032807', 'Neonatal seizure', 'XPO:0100056', 'abnormal olfactory epithelium', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(416029, 'HP:0032807', 'Neonatal seizure', 'XPO:0101133', 'abnormal motor neuron', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(416030, 'HP:0032807', 'Neonatal seizure', 'XPO:0101004', 'abnormal acid secreting cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(416031, 'HP:0032807', 'Neonatal seizure', 'XPO:0100691', 'abnormal keratin accumulating cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(416032, 'HP:0032807', 'Neonatal seizure', 'XPO:0100158', 'abnormal neuromere', 0.43333333333333335, 3.94131651835137, 1.3068679445984308, 'UPHENO:0004523', 'abnormal nervous system'),
(416033, 'HP:0032807', 'Neonatal seizure', 'XPO:0100081', 'abnormal anatomical entity in vitro', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416034, 'HP:0032807', 'Neonatal seizure', 'XPO:0100164', 'abnormal neural nucleus', 0.4482758620689655, 3.94131651835137, 1.3292091859262085, 'UPHENO:0004523', 'abnormal nervous system'),
(416035, 'HP:0032807', 'Neonatal seizure', 'XPO:0126887', 'abnormally localised nervous system', 0.4117647058823529, 3.94131651835137, 1.2739289764222381, 'UPHENO:0004523', 'abnormal nervous system'),
(416036, 'HP:0032807', 'Neonatal seizure', 'XPO:0100916', 'abnormal principal cavity', 0.43333333333333335, 3.94131651835137, 1.3068679445984308, 'UPHENO:0004523', 'abnormal nervous system'),
(416037, 'HP:0032807', 'Neonatal seizure', 'XPO:0101241', 'abnormal nucleate erythrocyte', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(416038, 'HP:0032807', 'Neonatal seizure', 'XPO:0100006', 'abnormal anatomical structure', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416039, 'HP:0032807', 'Neonatal seizure', 'XPO:0100701', 'abnormal microglial cell', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(416040, 'HP:0032807', 'Neonatal seizure', 'XPO:0100481', 'abnormal anatomical line', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416041, 'HP:0032807', 'Neonatal seizure', 'XPO:0101333', 'abnormal barrier epithelial cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(416042, 'HP:0032807', 'Neonatal seizure', 'XPO:0100273', 'abnormal visual system', 0.4642857142857143, 3.94131651835137, 1.3527368387638634, 'UPHENO:0004523', 'abnormal nervous system'),
(416043, 'HP:0032807', 'Neonatal seizure', 'XPO:0100427', 'abnormal olfactory system', 0.4642857142857143, 3.94131651835137, 1.3527368387638634, 'UPHENO:0004523', 'abnormal nervous system'),
(416044, 'HP:0032807', 'Neonatal seizure', 'XPO:0100114', 'abnormal peripheral nervous system', 0.4482758620689655, 3.94131651835137, 1.3292091859262085, 'UPHENO:0004523', 'abnormal nervous system'),
(416045, 'HP:0032807', 'Neonatal seizure', 'XPO:0101501', 'abnormal parabrachial area', 0.43333333333333335, 3.94131651835137, 1.3068679445984308, 'UPHENO:0004523', 'abnormal nervous system'),
(416046, 'HP:0032807', 'Neonatal seizure', 'XPO:0100653', 'abnormal myoblast', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(416047, 'HP:0032807', 'Neonatal seizure', 'XPO:0101435', 'abnormal paracrine cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(416048, 'HP:0032807', 'Neonatal seizure', 'XPO:0100438', 'abnormal spinal cord', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(416049, 'HP:0032807', 'Neonatal seizure', 'XPO:0101239', 'abnormal olfactory epithelial support cell', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(416050, 'HP:0032807', 'Neonatal seizure', 'XPO:0101132', 'abnormal apoptotic cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(416051, 'HP:0032807', 'Neonatal seizure', 'XPO:0101467', 'abnormal alkali secreting cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(416052, 'HP:0032807', 'Neonatal seizure', 'XPO:0101187', 'abnormal dorsolateral commissural neuron', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(416053, 'HP:0001311', 'Abnormal nervous system electrophysiology', 'XPO:0100916', 'abnormal principal cavity', 0.4482758620689655, 3.94131651835137, 1.3292091859262085, 'UPHENO:0004523', 'abnormal nervous system'),
(416054, 'HP:0001311', 'Abnormal nervous system electrophysiology', 'XPO:0100459', 'abnormal optic vesicle', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(416055, 'HP:0001311', 'Abnormal nervous system electrophysiology', 'XPO:0100549', 'abnormal mitotic cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(416056, 'HP:0001311', 'Abnormal nervous system electrophysiology', 'XPO:0100969', 'abnormal disaggregated/reaggregated ectoderm treated with activin', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416057, 'HP:0001311', 'Abnormal nervous system electrophysiology', 'XPO:0101435', 'abnormal paracrine cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(416058, 'HP:0001311', 'Abnormal nervous system electrophysiology', 'XPO:0100902', 'abnormal spermatocyte', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(416059, 'HP:0001311', 'Abnormal nervous system electrophysiology', 'XPO:0107286', 'abnormal efferent neuron', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(416060, 'HP:0001311', 'Abnormal nervous system electrophysiology', 'XPO:0131654', 'abnormal neuron projection', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(416061, 'HP:0001311', 'Abnormal nervous system electrophysiology', 'XPO:0100427', 'abnormal olfactory system', 0.48148148148148145, 3.94131651835137, 1.3775597686645948, 'UPHENO:0004523', 'abnormal nervous system'),
(416062, 'HP:0001311', 'Abnormal nervous system electrophysiology', 'XPO:0101264', 'abnormal mitotic spindle', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(416063, 'HP:0001311', 'Abnormal nervous system electrophysiology', 'XPO:0131666', 'abnormal adherens junction', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(416064, 'HP:0001311', 'Abnormal nervous system electrophysiology', 'XPO:0100674', 'abnormal secondary oogonium', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(416065, 'HP:0001311', 'Abnormal nervous system electrophysiology', 'XPO:0101514', 'abnormal dendrite', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(416066, 'HP:0001311', 'Abnormal nervous system electrophysiology', 'XPO:0142051', 'abnormal cerebrospinal fluid', 0.4642857142857143, 3.94131651835137, 1.3527368387638634, 'UPHENO:0004523', 'abnormal nervous system'),
(416067, 'HP:0001311', 'Abnormal nervous system electrophysiology', 'XPO:0100501', 'abnormal urogenital system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(416068, 'HP:0001311', 'Abnormal nervous system electrophysiology', 'XPO:0100285', 'abnormal progenitor cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(416069, 'HP:0001311', 'Abnormal nervous system electrophysiology', 'XPO:0101513', 'abnormal basal body', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(416070, 'HP:0001311', 'Abnormal nervous system electrophysiology', 'XPO:0101547', 'abnormal lampbrush chromosome', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(416071, 'HP:0001311', 'Abnormal nervous system electrophysiology', 'XPO:0100724', 'abnormal kinetochore', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(416072, 'HP:0001311', 'Abnormal nervous system electrophysiology', 'XPO:0100626', 'abnormal primordial germ cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(416073, 'HP:0001311', 'Abnormal nervous system electrophysiology', 'XPO:0100081', 'abnormal anatomical entity in vitro', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416074, 'HP:0001311', 'Abnormal nervous system electrophysiology', 'XPO:0100691', 'abnormal keratin accumulating cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(416075, 'HP:0001311', 'Abnormal nervous system electrophysiology', 'XPO:0100976', 'abnormal multiciliated cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(416076, 'HP:0001311', 'Abnormal nervous system electrophysiology', 'XPO:0100802', 'abnormal exocrine cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(416077, 'HP:0001311', 'Abnormal nervous system electrophysiology', 'XPO:0107253', 'abnormal enteric nervous system', 0.5, 3.94131651835137, 1.4038013602984167, 'UPHENO:0004523', 'abnormal nervous system'),
(416078, 'HP:0001311', 'Abnormal nervous system electrophysiology', 'XPO:0101373', 'abnormal oxygen accumulating cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(416079, 'HP:0001311', 'Abnormal nervous system electrophysiology', 'XPO:0100481', 'abnormal anatomical line', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416080, 'HP:0001311', 'Abnormal nervous system electrophysiology', 'XPO:0101664', 'abnormal nervous system morphology', 0.4117647058823529, 3.94131651835137, 1.2739289764222381, 'UPHENO:0004523', 'abnormal nervous system'),
(416081, 'HP:0001311', 'Abnormal nervous system electrophysiology', 'XPO:0142024', 'abnormally localised cerebrospinal fluid', 0.4117647058823529, 3.94131651835137, 1.2739289764222381, 'UPHENO:0004523', 'abnormal nervous system'),
(416082, 'HP:0001311', 'Abnormal nervous system electrophysiology', 'XPO:0100258', 'abnormal organ part', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416083, 'HP:0001311', 'Abnormal nervous system electrophysiology', 'XPO:0100734', 'abnormal lateral line system', 0.43333333333333335, 3.94131651835137, 1.3068679445984308, 'UPHENO:0004523', 'abnormal nervous system'),
(416084, 'HP:0001311', 'Abnormal nervous system electrophysiology', 'XPO:0100437', 'abnormal proepicardium', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(416085, 'HP:0001311', 'Abnormal nervous system electrophysiology', 'XPO:0100686', 'abnormal olfactory organ', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(416086, 'HP:0001311', 'Abnormal nervous system electrophysiology', 'XPO:0100954', 'abnormal neural progenitor cell', 0.43333333333333335, 3.94131651835137, 1.3068679445984308, 'UPHENO:0004523', 'abnormal nervous system'),
(416087, 'HP:0001311', 'Abnormal nervous system electrophysiology', 'XPO:0101297', 'abnormal barrier cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(416088, 'HP:0001311', 'Abnormal nervous system electrophysiology', 'XPO:0100754', 'abnormal electrically active cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(416089, 'HP:0001311', 'Abnormal nervous system electrophysiology', 'XPO:0100225', 'abnormal endocrine system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(416090, 'HP:0001311', 'Abnormal nervous system electrophysiology', 'XPO:0107287', 'abnormal afferent neuron', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(416091, 'HP:0001311', 'Abnormal nervous system electrophysiology', 'XPO:0101345', 'abnormal ascending interneuron', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(416092, 'HP:0001311', 'Abnormal nervous system electrophysiology', 'XPO:0100335', 'abnormal commissural interneuron', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(416093, 'HP:0001311', 'Abnormal nervous system electrophysiology', 'XPO:0101467', 'abnormal alkali secreting cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(416094, 'HP:0001311', 'Abnormal nervous system electrophysiology', 'XPO:0126887', 'abnormally localised nervous system', 0.42424242424242425, 3.94131651835137, 1.2930868781532416, 'UPHENO:0004523', 'abnormal nervous system'),
(416095, 'HP:0001311', 'Abnormal nervous system electrophysiology', 'XPO:0100721', 'abnormal centromere', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(416096, 'HP:0001311', 'Abnormal nervous system electrophysiology', 'XPO:0107258', 'abnormal anatomical axis', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416097, 'HP:0001311', 'Abnormal nervous system electrophysiology', 'XPO:0101535', 'abnormal absorptive cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(416098, 'HP:0001311', 'Abnormal nervous system electrophysiology', 'XPO:0126486', 'abnormally localised sensory system', 0.4117647058823529, 3.94131651835137, 1.2739289764222381, 'UPHENO:0004523', 'abnormal nervous system'),
(416099, 'HP:0001311', 'Abnormal nervous system electrophysiology', 'XPO:0131667', 'abnormal actin cytoskeleton', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(416100, 'HP:0001311', 'Abnormal nervous system electrophysiology', 'XPO:0100642', 'abnormal gustatory system', 0.48148148148148145, 3.94131651835137, 1.3775597686645948, 'UPHENO:0004523', 'abnormal nervous system'),
(416101, 'HP:0001311', 'Abnormal nervous system electrophysiology', 'XPO:0101501', 'abnormal parabrachial area', 0.4482758620689655, 3.94131651835137, 1.3292091859262085, 'UPHENO:0004523', 'abnormal nervous system'),
(416102, 'HP:0001311', 'Abnormal nervous system electrophysiology', 'XPO:0100638', 'abnormal polar body', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(416103, 'HP:0001311', 'Abnormal nervous system electrophysiology', 'XPO:0101004', 'abnormal acid secreting cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(416104, 'HP:0001311', 'Abnormal nervous system electrophysiology', 'XPO:0100907', 'abnormal cytoplasm', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(416105, 'HP:0001311', 'Abnormal nervous system electrophysiology', 'XPO:0100570', 'abnormal axon', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(416106, 'HP:0001311', 'Abnormal nervous system electrophysiology', 'XPO:0101569', 'abnormal activin-induced ectoderm', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416107, 'HP:0001311', 'Abnormal nervous system electrophysiology', 'XPO:0100649', 'abnormal growth cone', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(416108, 'HP:0001311', 'Abnormal nervous system electrophysiology', 'XPO:0100581', 'abnormal immune system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(416109, 'HP:0001311', 'Abnormal nervous system electrophysiology', 'XPO:0100477', 'abnormal pericyte', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(416110, 'HP:0001311', 'Abnormal nervous system electrophysiology', 'XPO:0100537', 'abnormal medium cavity', 0.4482758620689655, 3.94131651835137, 1.3292091859262085, 'UPHENO:0004523', 'abnormal nervous system'),
(416111, 'HP:0001311', 'Abnormal nervous system electrophysiology', 'XPO:0100445', 'abnormal spinal ganglion', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(416112, 'HP:0001311', 'Abnormal nervous system electrophysiology', 'XPO:0100025', 'abnormal oocyte', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(416113, 'HP:0001311', 'Abnormal nervous system electrophysiology', 'XPO:0101241', 'abnormal nucleate erythrocyte', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(416114, 'HP:0001311', 'Abnormal nervous system electrophysiology', 'XPO:0100372', 'abnormal hematological system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(416115, 'HP:0001311', 'Abnormal nervous system electrophysiology', 'XPO:0100587', 'abnormal vestibuloauditory system', 0.48148148148148145, 3.94131651835137, 1.3775597686645948, 'UPHENO:0004523', 'abnormal nervous system'),
(416116, 'HP:0001311', 'Abnormal nervous system electrophysiology', 'XPO:0100196', 'abnormal neuron', 0.4482758620689655, 3.94131651835137, 1.3292091859262085, 'UPHENO:0004523', 'abnormal nervous system'),
(416117, 'HP:0001311', 'Abnormal nervous system electrophysiology', 'XPO:0100336', 'abnormal interneuron', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(416118, 'HP:0001311', 'Abnormal nervous system electrophysiology', 'XPO:0100773', 'abnormal profundus ganglion', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(416119, 'HP:0001311', 'Abnormal nervous system electrophysiology', 'XPO:0100006', 'abnormal anatomical structure', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416120, 'HP:0001311', 'Abnormal nervous system electrophysiology', 'XPO:0100899', 'abnormal secondary spermatogonium', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(416121, 'HP:0001311', 'Abnormal nervous system electrophysiology', 'XPO:0100894', 'abnormal nucleus', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(416122, 'HP:0001311', 'Abnormal nervous system electrophysiology', 'XPO:0100533', 'abnormal melanoblast', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(416123, 'HP:0001311', 'Abnormal nervous system electrophysiology', 'XPO:0101071', 'abnormal endoplasmic reticulum', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(416124, 'HP:0001311', 'Abnormal nervous system electrophysiology', 'XPO:0100136', 'abnormal neural tube', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(416125, 'HP:0001311', 'Abnormal nervous system electrophysiology', 'XPO:0100273', 'abnormal visual system', 0.48148148148148145, 3.94131651835137, 1.3775597686645948, 'UPHENO:0004523', 'abnormal nervous system'),
(416126, 'HP:0001311', 'Abnormal nervous system electrophysiology', 'XPO:0101187', 'abnormal dorsolateral commissural neuron', 0.43333333333333335, 3.94131651835137, 1.3068679445984308, 'UPHENO:0004523', 'abnormal nervous system'),
(416127, 'HP:0001311', 'Abnormal nervous system electrophysiology', 'XPO:0100004', 'abnormal cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(416128, 'HP:0001311', 'Abnormal nervous system electrophysiology', 'XPO:0141841', 'abnormality of whole organism mass', 0.41379310344827586, 2.13901709234296, 0.9408031255100615, 'UPHENO:0075696', 'abnormal anatomical entity'),
(416129, 'HP:0001311', 'Abnormal nervous system electrophysiology', 'XPO:0100653', 'abnormal myoblast', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(416130, 'HP:0001311', 'Abnormal nervous system electrophysiology', 'XPO:0100026', 'abnormal germ cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(416131, 'HP:0001311', 'Abnormal nervous system electrophysiology', 'XPO:0100274', 'abnormal sensory system', 0.5, 3.94131651835137, 1.4038013602984167, 'UPHENO:0004523', 'abnormal nervous system'),
(416132, 'HP:0001311', 'Abnormal nervous system electrophysiology', 'XPO:0101061', 'abnormal plasma membrane', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(416133, 'HP:0001311', 'Abnormal nervous system electrophysiology', 'XPO:0100864', 'abnormal dorsolateral ascending neuron', 0.43333333333333335, 3.94131651835137, 1.3068679445984308, 'UPHENO:0004523', 'abnormal nervous system'),
(416134, 'HP:0001311', 'Abnormal nervous system electrophysiology', 'XPO:0101448', 'abnormal myelin accumulating cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(416135, 'HP:0001311', 'Abnormal nervous system electrophysiology', 'XPO:0100515', 'abnormal somatic stem cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(416136, 'HP:0001311', 'Abnormal nervous system electrophysiology', 'XPO:0101485', 'abnormal descending interneuron', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(416137, 'HP:0001311', 'Abnormal nervous system electrophysiology', 'XPO:0142057', 'abnormal desmosome', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(416138, 'HP:0001311', 'Abnormal nervous system electrophysiology', 'XPO:0101141', 'abnormal Keller explant', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416139, 'HP:0001311', 'Abnormal nervous system electrophysiology', 'XPO:0100358', 'abnormal ganglion', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(416140, 'HP:0001311', 'Abnormal nervous system electrophysiology', 'XPO:0100317', 'abnormal respiratory system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(416141, 'HP:0001311', 'Abnormal nervous system electrophysiology', 'XPO:0100164', 'abnormal neural nucleus', 0.4642857142857143, 3.94131651835137, 1.3527368387638634, 'UPHENO:0004523', 'abnormal nervous system'),
(416142, 'HP:0001311', 'Abnormal nervous system electrophysiology', 'XPO:0101228', 'abnormal mesenchymal stem cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(416143, 'HP:0001311', 'Abnormal nervous system electrophysiology', 'XPO:0101132', 'abnormal apoptotic cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(416144, 'HP:0001311', 'Abnormal nervous system electrophysiology', 'XPO:0100852', 'abnormal interdigital region', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(416145, 'HP:0001311', 'Abnormal nervous system electrophysiology', 'XPO:0100114', 'abnormal peripheral nervous system', 0.4642857142857143, 3.94131651835137, 1.3527368387638634, 'UPHENO:0004523', 'abnormal nervous system'),
(416146, 'HP:0001311', 'Abnormal nervous system electrophysiology', 'XPO:0100108', 'abnormal cell part', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(416147, 'HP:0001311', 'Abnormal nervous system electrophysiology', 'XPO:0100429', 'abnormal spermatid', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(416148, 'HP:0001311', 'Abnormal nervous system electrophysiology', 'XPO:0100888', 'abnormal microtubule', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(416149, 'HP:0001311', 'Abnormal nervous system electrophysiology', 'XPO:0100760', 'abnormal Stirnorgan', 0.43333333333333335, 3.94131651835137, 1.3068679445984308, 'UPHENO:0004523', 'abnormal nervous system'),
(416150, 'HP:0001311', 'Abnormal nervous system electrophysiology', 'XPO:0100956', 'abnormal centrosome', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(416151, 'HP:0001311', 'Abnormal nervous system electrophysiology', 'XPO:0100438', 'abnormal spinal cord', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(416152, 'HP:0001311', 'Abnormal nervous system electrophysiology', 'XPO:0100858', 'abnormal presumptive midbrain-hindbrain boundary', 0.4482758620689655, 3.94131651835137, 1.3292091859262085, 'UPHENO:0004523', 'abnormal nervous system'),
(416153, 'HP:0001311', 'Abnormal nervous system electrophysiology', 'XPO:0141625', 'metaplastic spinal cord', 0.4117647058823529, 3.94131651835137, 1.2739289764222381, 'UPHENO:0004523', 'abnormal nervous system'),
(416154, 'HP:0001311', 'Abnormal nervous system electrophysiology', 'XPO:0115758', 'abnormally decreased mobility of melanoblast', 0.41379310344827586, 2.13901709234296, 0.9408031255100615, 'UPHENO:0075696', 'abnormal anatomical entity'),
(416155, 'HP:0001311', 'Abnormal nervous system electrophysiology', 'XPO:0100232', 'abnormal lymphatic system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(416156, 'HP:0001311', 'Abnormal nervous system electrophysiology', 'XPO:0100344', 'abnormal portion of organism substance', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416157, 'HP:0001311', 'Abnormal nervous system electrophysiology', 'XPO:0100032', 'abnormal nervous system', 0.52, 3.94131651835137, 1.4316021058739445, 'UPHENO:0004523', 'abnormal nervous system'),
(416158, 'HP:0001311', 'Abnormal nervous system electrophysiology', 'XPO:0101240', 'abnormal ciliated non-epidermal cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(416159, 'HP:0001311', 'Abnormal nervous system electrophysiology', 'XPO:0100056', 'abnormal olfactory epithelium', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(416160, 'HP:0001311', 'Abnormal nervous system electrophysiology', 'XPO:0107284', 'abnormal migrating myoblast', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(416161, 'HP:0001311', 'Abnormal nervous system electrophysiology', 'XPO:0100031', 'abnormal central nervous system', 0.5, 3.94131651835137, 1.4038013602984167, 'UPHENO:0004523', 'abnormal nervous system'),
(416162, 'HP:0001311', 'Abnormal nervous system electrophysiology', 'XPO:0100175', 'abnormal migrating neuroblast', 0.4482758620689655, 3.94131651835137, 1.3292091859262085, 'UPHENO:0004523', 'abnormal nervous system'),
(416163, 'HP:0001311', 'Abnormal nervous system electrophysiology', 'XPO:0100701', 'abnormal microglial cell', 0.43333333333333335, 3.94131651835137, 1.3068679445984308, 'UPHENO:0004523', 'abnormal nervous system'),
(416164, 'HP:0001311', 'Abnormal nervous system electrophysiology', 'XPO:0100308', 'abnormal early embryonic cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(416165, 'HP:0001311', 'Abnormal nervous system electrophysiology', 'XPO:0101326', 'abnormal cementoblast', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(416166, 'HP:0001311', 'Abnormal nervous system electrophysiology', 'XPO:0100546', 'abnormal whole organism', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416167, 'HP:0001311', 'Abnormal nervous system electrophysiology', 'XPO:0100172', 'abnormal stem cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(416168, 'HP:0001311', 'Abnormal nervous system electrophysiology', 'XPO:0107312', 'abnormal filopodium', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(416169, 'HP:0001311', 'Abnormal nervous system electrophysiology', 'XPO:0100715', 'abnormal ciliated cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(416170, 'HP:0001311', 'Abnormal nervous system electrophysiology', 'XPO:0100704', 'abnormal Merkel cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(416171, 'HP:0001311', 'Abnormal nervous system electrophysiology', 'XPO:0101333', 'abnormal barrier epithelial cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(416172, 'HP:0001311', 'Abnormal nervous system electrophysiology', 'XPO:0100702', 'abnormal glial cell', 0.4482758620689655, 3.94131651835137, 1.3292091859262085, 'UPHENO:0004523', 'abnormal nervous system'),
(416173, 'HP:0001311', 'Abnormal nervous system electrophysiology', 'XPO:0125261', 'absent nervous system', 0.4117647058823529, 3.94131651835137, 1.2739289764222381, 'UPHENO:0004523', 'abnormal nervous system'),
(416174, 'HP:0001311', 'Abnormal nervous system electrophysiology', 'XPO:0101239', 'abnormal olfactory epithelial support cell', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(416175, 'HP:0001311', 'Abnormal nervous system electrophysiology', 'XPO:0100289', 'abnormal chondroblast', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(416176, 'HP:0001311', 'Abnormal nervous system electrophysiology', 'XPO:0101110', 'abnormal cell-free extract', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416177, 'HP:0001311', 'Abnormal nervous system electrophysiology', 'XPO:0101133', 'abnormal motor neuron', 0.43333333333333335, 3.94131651835137, 1.3068679445984308, 'UPHENO:0004523', 'abnormal nervous system'),
(416178, 'HP:0001311', 'Abnormal nervous system electrophysiology', 'XPO:0107257', 'abnormal peripheral ganglion', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(416179, 'HP:0001311', 'Abnormal nervous system electrophysiology', 'XPO:0100158', 'abnormal neuromere', 0.4482758620689655, 3.94131651835137, 1.3292091859262085, 'UPHENO:0004523', 'abnormal nervous system'),
(416180, 'HP:0001311', 'Abnormal nervous system electrophysiology', 'XPO:0101370', 'abnormal floor plate', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(416181, 'HP:0001311', 'Abnormal nervous system electrophysiology', 'XPO:0100791', 'abnormal multiciliated cell precursor', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(416182, 'HP:0001311', 'Abnormal nervous system electrophysiology', 'XPO:0101237', 'abnormal mucus secreting cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(416183, 'HP:0001311', 'Abnormal nervous system electrophysiology', 'XPO:0100817', 'abnormal intersomitic neuron', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(416184, 'HP:0001311', 'Abnormal nervous system electrophysiology', 'XPO:0100337', 'abnormal zygote', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(416185, 'HP:5201008', 'Complete cleft maxillary alveolar ridge', 'XPO:0129225', 'decreased size of the upper jaw', 0.5108695652173914, 8.608423498638606, 2.097088832156778, 'UPHENO:0088116', 'abnormal jaw skeleton morphology'),
(416186, 'HP:5201008', 'Complete cleft maxillary alveolar ridge', 'XPO:0129152', 'decreased size of the oral cavity', 0.40229885057471265, 7.884497199543557, 1.7809896576723612, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(416187, 'HP:5201008', 'Complete cleft maxillary alveolar ridge', 'XPO:0140626', 'abnormally necrotic tongue', 0.40229885057471265, 7.884497199543557, 1.7809896576723612, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(416188, 'HP:5201008', 'Complete cleft maxillary alveolar ridge', 'XPO:0140639', 'abnormally necrotic upper jaw', 0.5222222222222223, 8.608423498638606, 2.1202617879141834, 'UPHENO:0088116', 'abnormal jaw skeleton morphology'),
(416189, 'HP:5201008', 'Complete cleft maxillary alveolar ridge', 'XPO:0130358', 'increased size of the lower jaw', 0.5222222222222223, 8.608423498638606, 2.1202617879141834, 'UPHENO:0088116', 'abnormal jaw skeleton morphology'),
(416190, 'HP:5201008', 'Complete cleft maxillary alveolar ridge', 'XPO:0102279', 'abnormal mouth morphology', 0.4024390243902439, 7.312692920701687, 1.7154920590526295, 'UPHENO:0076800', 'abnormal mouth morphology'),
(416191, 'HP:5201008', 'Complete cleft maxillary alveolar ridge', 'XPO:0103199', 'abnormal tongue morphology', 0.4268292682926829, 7.884497199543557, 1.8344847152639032, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(416192, 'HP:5201008', 'Complete cleft maxillary alveolar ridge', 'XPO:0130628', 'increased size of the oral cavity', 0.40229885057471265, 7.884497199543557, 1.7809896576723612, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(416193, 'HP:5201008', 'Complete cleft maxillary alveolar ridge', 'XPO:0140524', 'abnormally necrotic Meckels cartilage', 0.40869565217391307, 8.608423498638606, 1.8756932734232812, 'UPHENO:0088116', 'abnormal jaw skeleton morphology'),
(416194, 'HP:5201008', 'Complete cleft maxillary alveolar ridge', 'XPO:0102921', 'abnormal orbital region morphology', 0.41379310344827586, 8.057231734572694, 1.8259317962757453, 'UPHENO:0084457', 'abnormal facial skeleton morphology'),
(416195, 'HP:5201008', 'Complete cleft maxillary alveolar ridge', 'XPO:0103096', 'abnormal oral cavity morphology', 0.4268292682926829, 7.884497199543557, 1.8344847152639032, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(416196, 'HP:5201008', 'Complete cleft maxillary alveolar ridge', 'XPO:0101567', 'abnormal tongue', 0.42105263157894735, 7.884497199543557, 1.8220286206711067, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(416197, 'HP:5201008', 'Complete cleft maxillary alveolar ridge', 'XPO:0140665', 'abnormally necrotic processus retroarticularis of Meckels cartilage', 0.4017094017094017, 8.608423498638606, 1.8595926041203943, 'UPHENO:0088116', 'abnormal jaw skeleton morphology'),
(416198, 'HP:5201008', 'Complete cleft maxillary alveolar ridge', 'XPO:0101816', 'abnormal tooth morphology', 0.4166666666666667, 7.884497199543557, 1.812514045870123, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(416199, 'HP:5201008', 'Complete cleft maxillary alveolar ridge', 'XPO:0130701', 'increased size of the upper jaw', 0.5108695652173914, 8.608423498638606, 2.097088832156778, 'UPHENO:0088116', 'abnormal jaw skeleton morphology'),
(416200, 'HP:5201008', 'Complete cleft maxillary alveolar ridge', 'XPO:0128880', 'decreased size of the lower jaw', 0.5222222222222223, 8.608423498638606, 2.1202617879141834, 'UPHENO:0088116', 'abnormal jaw skeleton morphology'),
(416201, 'HP:5201008', 'Complete cleft maxillary alveolar ridge', 'XPO:0102398', 'abnormal Meckels cartilage morphology', 0.44339622641509435, 8.608423498638606, 1.9536996940879583, 'UPHENO:0088116', 'abnormal jaw skeleton morphology'),
(416202, 'HP:5201008', 'Complete cleft maxillary alveolar ridge', 'XPO:0102337', 'abnormal processus retroarticularis of Meckels cartilage morphology', 0.4351851851851852, 8.608423498638606, 1.9355253484280543, 'UPHENO:0088116', 'abnormal jaw skeleton morphology'),
(416203, 'HP:5201008', 'Complete cleft maxillary alveolar ridge', 'XPO:0140897', 'abnormally necrotic lower jaw', 0.5340909090909091, 8.608423498638606, 2.1442203086967155, 'UPHENO:0088116', 'abnormal jaw skeleton morphology'),
(416204, 'HP:5201008', 'Complete cleft maxillary alveolar ridge', 'XPO:0101659', 'abnormal lower jaw morphology', 0.5662650602409639, 8.608423498638606, 2.207860831446656, 'UPHENO:0088116', 'abnormal jaw skeleton morphology'),
(416205, 'HP:5201008', 'Complete cleft maxillary alveolar ridge', 'XPO:0103138', 'abnormal upper jaw morphology', 0.5529411764705883, 8.608423498638606, 2.1817313805540515, 'UPHENO:0088116', 'abnormal jaw skeleton morphology'),
(416206, 'HP:0002465', 'Poor speech', 'XPO:0100175', 'abnormal migrating neuroblast', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(416207, 'HP:0002465', 'Poor speech', 'XPO:0100864', 'abnormal dorsolateral ascending neuron', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(416208, 'HP:0002465', 'Poor speech', 'XPO:0100954', 'abnormal neural progenitor cell', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(416209, 'HP:0002465', 'Poor speech', 'XPO:0100858', 'abnormal presumptive midbrain-hindbrain boundary', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(416210, 'HP:0002465', 'Poor speech', 'XPO:0101501', 'abnormal parabrachial area', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(416211, 'HP:0002465', 'Poor speech', 'XPO:0100734', 'abnormal lateral line system', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(416212, 'HP:0002465', 'Poor speech', 'XPO:0100196', 'abnormal neuron', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(416213, 'HP:0002465', 'Poor speech', 'XPO:0101187', 'abnormal dorsolateral commissural neuron', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(416214, 'HP:0002465', 'Poor speech', 'XPO:0100427', 'abnormal olfactory system', 0.4482758620689655, 3.94131651835137, 1.3292091859262085, 'UPHENO:0004523', 'abnormal nervous system'),
(416215, 'HP:0002465', 'Poor speech', 'XPO:0100032', 'abnormal nervous system', 0.48148148148148145, 3.94131651835137, 1.3775597686645948, 'UPHENO:0004523', 'abnormal nervous system'),
(416216, 'HP:0002465', 'Poor speech', 'XPO:0100916', 'abnormal principal cavity', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(416217, 'HP:0002465', 'Poor speech', 'XPO:0100273', 'abnormal visual system', 0.4482758620689655, 3.94131651835137, 1.3292091859262085, 'UPHENO:0004523', 'abnormal nervous system'),
(416218, 'HP:0002465', 'Poor speech', 'XPO:0100004', 'abnormal cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(416219, 'HP:0002465', 'Poor speech', 'XPO:0100642', 'abnormal gustatory system', 0.4482758620689655, 3.94131651835137, 1.3292091859262085, 'UPHENO:0004523', 'abnormal nervous system'),
(416220, 'HP:0002465', 'Poor speech', 'XPO:0100158', 'abnormal neuromere', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(416221, 'HP:0002465', 'Poor speech', 'XPO:0107253', 'abnormal enteric nervous system', 0.4642857142857143, 3.94131651835137, 1.3527368387638634, 'UPHENO:0004523', 'abnormal nervous system'),
(416222, 'HP:0002465', 'Poor speech', 'XPO:0100587', 'abnormal vestibuloauditory system', 0.4482758620689655, 3.94131651835137, 1.3292091859262085, 'UPHENO:0004523', 'abnormal nervous system'),
(416223, 'HP:0002465', 'Poor speech', 'XPO:0100537', 'abnormal medium cavity', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(416224, 'HP:0002465', 'Poor speech', 'XPO:0100031', 'abnormal central nervous system', 0.4642857142857143, 3.94131651835137, 1.3527368387638634, 'UPHENO:0004523', 'abnormal nervous system'),
(416225, 'HP:0002465', 'Poor speech', 'XPO:0100114', 'abnormal peripheral nervous system', 0.43333333333333335, 3.94131651835137, 1.3068679445984308, 'UPHENO:0004523', 'abnormal nervous system'),
(416226, 'HP:0002465', 'Poor speech', 'XPO:0100274', 'abnormal sensory system', 0.4642857142857143, 3.94131651835137, 1.3527368387638634, 'UPHENO:0004523', 'abnormal nervous system'),
(416227, 'HP:0002465', 'Poor speech', 'XPO:0100760', 'abnormal Stirnorgan', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(416228, 'HP:0002465', 'Poor speech', 'XPO:0100701', 'abnormal microglial cell', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(416229, 'HP:0002465', 'Poor speech', 'XPO:0100164', 'abnormal neural nucleus', 0.43333333333333335, 3.94131651835137, 1.3068679445984308, 'UPHENO:0004523', 'abnormal nervous system'),
(416230, 'HP:0002465', 'Poor speech', 'XPO:0101133', 'abnormal motor neuron', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(416231, 'HP:0002465', 'Poor speech', 'XPO:0142051', 'abnormal cerebrospinal fluid', 0.43333333333333335, 3.94131651835137, 1.3068679445984308, 'UPHENO:0004523', 'abnormal nervous system'),
(416232, 'HP:0002465', 'Poor speech', 'XPO:0100702', 'abnormal glial cell', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(416233, 'HP:0032587', 'Renal interstitial calcium oxalate', 'XPO:0100147', 'abnormal mesonephric mesenchyme', 0.5277777777777778, 6.880013295263146, 1.9055492982485522, 'HP:0000077', 'Abnormality of the kidney'),
(416234, 'HP:0032587', 'Renal interstitial calcium oxalate', 'XPO:0125038', 'absent embryonic kidney', 0.40350877192982454, 7.603795021646889, 1.7516272409365097, 'HP:0012210', 'Abnormal renal morphology'),
(416235, 'HP:0032587', 'Renal interstitial calcium oxalate', 'XPO:0102393', 'abnormal ureter morphology', 0.41304347826086957, 7.340144605965611, 1.7412061506282923, 'UPHENO:0087427', 'abnormal renal system morphology'),
(416236, 'HP:0032587', 'Renal interstitial calcium oxalate', 'XPO:0141643', 'neoplastic kidney', 0.46938775510204084, 7.603795021646889, 1.8892136659115366, 'HP:0012210', 'Abnormal renal morphology'),
(416237, 'HP:0032587', 'Renal interstitial calcium oxalate', 'XPO:0107301', 'abnormal adult kidney', 0.5, 6.880013295263146, 1.8547254911796445, 'HP:0000077', 'Abnormality of the kidney'),
(416238, 'HP:0032587', 'Renal interstitial calcium oxalate', 'XPO:0100270', 'abnormal mesonephric tubule', 0.40425531914893614, 6.880013295263146, 1.6677175931270638, 'HP:0000077', 'Abnormality of the kidney'),
(416239, 'HP:0032587', 'Renal interstitial calcium oxalate', 'XPO:0129822', 'increased size of the mesonephric mesenchyme', 0.41818181818181815, 7.603795021646889, 1.7831906312097294, 'HP:0012210', 'Abnormal renal morphology'),
(416240, 'HP:0032587', 'Renal interstitial calcium oxalate', 'XPO:0102198', 'abnormal kidney morphology', 0.5, 7.603795021646889, 1.9498455094759288, 'HP:0012210', 'Abnormal renal morphology'),
(416241, 'HP:0032587', 'Renal interstitial calcium oxalate', 'XPO:0126885', 'abnormally localised adult kidney', 0.4423076923076923, 7.603795021646889, 1.833907584586899, 'HP:0012210', 'Abnormal renal morphology'),
(416242, 'HP:0032587', 'Renal interstitial calcium oxalate', 'XPO:0126072', 'absent mesonephric sinus', 0.4318181818181818, 6.880013295263146, 1.7236341932224046, 'HP:0000077', 'Abnormality of the kidney'),
(416243, 'HP:0032587', 'Renal interstitial calcium oxalate', 'XPO:0125089', 'absent kidney', 0.41818181818181815, 7.603795021646889, 1.7831906312097294, 'HP:0012210', 'Abnormal renal morphology'),
(416244, 'HP:0032587', 'Renal interstitial calcium oxalate', 'XPO:0126710', 'abnormally localised kidney', 0.46, 7.603795021646889, 1.870226111986882, 'HP:0012210', 'Abnormal renal morphology'),
(416245, 'HP:0032587', 'Renal interstitial calcium oxalate', 'XPO:0107387', 'abnormal embryonic kidney morphology', 0.4791666666666667, 7.603795021646889, 1.9087915324988045, 'HP:0012210', 'Abnormal renal morphology'),
(416246, 'HP:0032587', 'Renal interstitial calcium oxalate', 'XPO:0100567', 'abnormal mesonephric collecting duct', 0.45098039215686275, 7.603795021646889, 1.8517997895946297, 'HP:0012210', 'Abnormal renal morphology'),
(416247, 'HP:0032587', 'Renal interstitial calcium oxalate', 'XPO:0129202', 'decreased size of the mesonephric sinus', 0.5227272727272727, 7.603795021646889, 1.9936677341128566, 'HP:0012210', 'Abnormal renal morphology'),
(416248, 'HP:0032587', 'Renal interstitial calcium oxalate', 'XPO:0140354', 'abnormally necrotic adult kidney', 0.40350877192982454, 7.603795021646889, 1.7516272409365097, 'HP:0012210', 'Abnormal renal morphology'),
(416249, 'HP:0032587', 'Renal interstitial calcium oxalate', 'XPO:0100566', 'abnormal kidney', 0.5135135135135135, 6.880013295263146, 1.8796222493549772, 'HP:0000077', 'Abnormality of the kidney'),
(416250, 'HP:0032587', 'Renal interstitial calcium oxalate', 'XPO:0101701', 'abnormal urinary system morphology', 0.4358974358974359, 7.340144605965611, 1.788728658253343, 'UPHENO:0087427', 'abnormal renal system morphology'),
(416251, 'HP:0032587', 'Renal interstitial calcium oxalate', 'XPO:0128342', 'decreased size of the mesonephric mesenchyme', 0.41818181818181815, 7.603795021646889, 1.7831906312097294, 'HP:0012210', 'Abnormal renal morphology'),
(416252, 'HP:0032587', 'Renal interstitial calcium oxalate', 'XPO:0139936', 'abnormally necrotic embryonic kidney', 0.40350877192982454, 7.603795021646889, 1.7516272409365097, 'HP:0012210', 'Abnormal renal morphology'),
(416253, 'HP:0032587', 'Renal interstitial calcium oxalate', 'XPO:0101717', 'abnormal mesonephric sinus morphology', 0.5897435897435898, 7.603795021646889, 2.1176140752602852, 'HP:0012210', 'Abnormal renal morphology'),
(416254, 'HP:0032587', 'Renal interstitial calcium oxalate', 'XPO:0125259', 'absent adult kidney', 0.40350877192982454, 7.603795021646889, 1.7516272409365097, 'HP:0012210', 'Abnormal renal morphology'),
(416255, 'HP:0032587', 'Renal interstitial calcium oxalate', 'XPO:0103182', 'abnormal pronephric sinus morphology', 0.42592592592592593, 7.603795021646889, 1.7996259153351557, 'HP:0012210', 'Abnormal renal morphology'),
(416256, 'HP:0032587', 'Renal interstitial calcium oxalate', 'XPO:0100565', 'abnormal pronephric kidney', 0.40425531914893614, 6.880013295263146, 1.6677175931270638, 'HP:0000077', 'Abnormality of the kidney'),
(416257, 'HP:0032587', 'Renal interstitial calcium oxalate', 'XPO:0100271', 'abnormal mesonephric nephron', 0.4318181818181818, 6.880013295263146, 1.7236341932224046, 'HP:0000077', 'Abnormality of the kidney'),
(416258, 'HP:0032587', 'Renal interstitial calcium oxalate', 'XPO:0130678', 'increased size of the mesonephric sinus', 0.5227272727272727, 7.603795021646889, 1.9936677341128566, 'HP:0012210', 'Abnormal renal morphology'),
(416259, 'HP:0032587', 'Renal interstitial calcium oxalate', 'XPO:0126656', 'abnormally localised embryonic kidney', 0.4423076923076923, 7.603795021646889, 1.833907584586899, 'HP:0012210', 'Abnormal renal morphology'),
(416260, 'HP:0032587', 'Renal interstitial calcium oxalate', 'XPO:0101779', 'abnormal mesonephric mesenchyme morphology', 0.48936170212765956, 7.603795021646889, 1.9289909472112474, 'HP:0012210', 'Abnormal renal morphology'),
(416261, 'HP:0032587', 'Renal interstitial calcium oxalate', 'XPO:0107300', 'abnormal embryonic kidney', 0.5, 6.880013295263146, 1.8547254911796445, 'HP:0000077', 'Abnormality of the kidney'),
(416262, 'HP:0032587', 'Renal interstitial calcium oxalate', 'XPO:0107388', 'abnormal adult kidney morphology', 0.4791666666666667, 7.603795021646889, 1.9087915324988045, 'HP:0012210', 'Abnormal renal morphology'),
(416263, 'HP:0032587', 'Renal interstitial calcium oxalate', 'XPO:0100085', 'abnormal mesonephric sinus', 0.5757575757575758, 6.880013295263146, 1.9902813308827976, 'HP:0000077', 'Abnormality of the kidney'),
(416264, 'HP:0032587', 'Renal interstitial calcium oxalate', 'XPO:0128275', 'decreased size of the kidney', 0.40350877192982454, 7.603795021646889, 1.7516272409365097, 'HP:0012210', 'Abnormal renal morphology'),
(416265, 'HP:0032587', 'Renal interstitial calcium oxalate', 'XPO:0127342', 'abnormally localised mesonephric mesenchyme', 0.40425531914893614, 6.880013295263146, 1.6677175931270638, 'HP:0000077', 'Abnormality of the kidney'),
(416266, 'HP:0032587', 'Renal interstitial calcium oxalate', 'XPO:0127733', 'abnormally localised mesonephric sinus', 0.475, 6.880013295263146, 1.8077627928602786, 'HP:0000077', 'Abnormality of the kidney'),
(416267, 'HP:0032587', 'Renal interstitial calcium oxalate', 'XPO:0141613', 'metaplastic kidney', 0.4634146341463415, 6.880013295263146, 1.7855808142300187, 'HP:0000077', 'Abnormality of the kidney'),
(416268, 'HP:0032587', 'Renal interstitial calcium oxalate', 'XPO:0100069', 'abnormal urinary system', 0.46875, 6.355235291121788, 1.725982775902859, 'HP:0000079', 'Abnormality of the urinary system'),
(416269, 'HP:0032587', 'Renal interstitial calcium oxalate', 'XPO:0100761', 'abnormal ureter', 0.4594594594594595, 6.828345551150745, 1.7712560390677927, 'HP:0010935', 'Abnormality of the upper urinary tract'),
(416270, 'HP:0032587', 'Renal interstitial calcium oxalate', 'XPO:0140552', 'abnormally necrotic kidney', 0.42592592592592593, 7.603795021646889, 1.7996259153351557, 'HP:0012210', 'Abnormal renal morphology'),
(416271, 'HP:0032587', 'Renal interstitial calcium oxalate', 'XPO:0140815', 'abnormally necrotic mesonephric mesenchyme', 0.4339622641509434, 7.603795021646889, 1.816524181984252, 'HP:0012210', 'Abnormal renal morphology'),
(416272, 'HP:0032587', 'Renal interstitial calcium oxalate', 'XPO:0101277', 'abnormal glomerulus', 0.4222222222222222, 6.880013295263146, 1.7043751061443133, 'HP:0000077', 'Abnormality of the kidney'),
(416273, 'HP:0032587', 'Renal interstitial calcium oxalate', 'XPO:0100501', 'abnormal urogenital system', 0.41935483870967744, 5.4478002382576385, 1.5114765596055648, 'HP:0000119', 'Abnormality of the genitourinary system'),
(416274, 'HP:0032587', 'Renal interstitial calcium oxalate', 'XPO:0102410', 'abnormal mesonephric kidney morphology', 0.41818181818181815, 7.603795021646889, 1.7831906312097294, 'HP:0012210', 'Abnormal renal morphology'),
(416275, 'HP:0032587', 'Renal interstitial calcium oxalate', 'XPO:0101903', 'abnormal mesonephric nephron morphology', 0.41818181818181815, 7.603795021646889, 1.7831906312097294, 'HP:0012210', 'Abnormal renal morphology'),
(416276, 'HP:0032587', 'Renal interstitial calcium oxalate', 'XPO:0100778', 'abnormal mesonephric kidney', 0.4418604651162791, 6.880013295263146, 1.7435612620872136, 'HP:0000077', 'Abnormality of the kidney'),
(416277, 'HP:0006265', 'Aplasia/Hypoplasia of fingers', 'XPO:0129161', 'decreased size of the forelimb digit 5', 0.46, 7.492661022682715, 1.8565085699866966, 'HP:0001167', 'Abnormal finger morphology'),
(416278, 'HP:0006265', 'Aplasia/Hypoplasia of fingers', 'XPO:0103755', 'increased size of the forelimb digit', 0.4791666666666667, 7.492661022682715, 1.8947911248214497, 'HP:0001167', 'Abnormal finger morphology'),
(416279, 'HP:0006265', 'Aplasia/Hypoplasia of fingers', 'XPO:0102598', 'abnormal forelimb digit 3 morphology', 0.5227272727272727, 7.492661022682715, 1.9790447852074682, 'HP:0001167', 'Abnormal finger morphology'),
(416280, 'HP:0006265', 'Aplasia/Hypoplasia of fingers', 'XPO:0100178', 'abnormal digit', 0.42424242424242425, 6.393467666143939, 1.6469305455909364, 'UPHENO:0002905', 'abnormal digit'),
(416281, 'HP:0006265', 'Aplasia/Hypoplasia of fingers', 'XPO:0141208', 'abnormally necrotic digit-joint region', 0.4473684210526316, 6.466375519622663, 1.7008386772845274, 'UPHENO:0086700', 'abnormal digit morphology'),
(416282, 'HP:0006265', 'Aplasia/Hypoplasia of fingers', 'XPO:0141143', 'abnormally necrotic forelimb digit 3', 0.4742268041237113, 7.492661022682715, 1.8849988570736913, 'HP:0001167', 'Abnormal finger morphology'),
(416283, 'HP:0006265', 'Aplasia/Hypoplasia of fingers', 'XPO:0100582', 'abnormal forelimb digit', 0.41025641025641024, 7.059765001318215, 1.701856000575446, 'UPHENO:0002708', 'abnormal manus'),
(416284, 'HP:0006265', 'Aplasia/Hypoplasia of fingers', 'XPO:0130637', 'increased size of the forelimb digit 5', 0.46464646464646464, 7.492661022682715, 1.8658613171894334, 'HP:0001167', 'Abnormal finger morphology'),
(416285, 'HP:0006265', 'Aplasia/Hypoplasia of fingers', 'XPO:0140898', 'abnormally necrotic forelimb digit 5', 0.4742268041237113, 7.492661022682715, 1.8849988570736913, 'HP:0001167', 'Abnormal finger morphology'),
(416286, 'HP:0006265', 'Aplasia/Hypoplasia of fingers', 'XPO:0141556', 'abnormal forelimb digit morphology in the regenerating forelimb', 0.5, 7.492661022682715, 1.935543983313569, 'HP:0001167', 'Abnormal finger morphology'),
(416287, 'HP:0006265', 'Aplasia/Hypoplasia of fingers', 'XPO:0139962', 'abnormally necrotic digit', 0.43037974683544306, 6.466375519622663, 1.6682317162427132, 'UPHENO:0086700', 'abnormal digit morphology'),
(416288, 'HP:0006265', 'Aplasia/Hypoplasia of fingers', 'XPO:0100897', 'abnormal forelimb digit 4', 0.4050632911392405, 7.059765001318215, 1.6910504564038238, 'UPHENO:0002708', 'abnormal manus'),
(416289, 'HP:0006265', 'Aplasia/Hypoplasia of fingers', 'XPO:0103821', 'decreased length of forelimb digit 2 in regenerating forelimb', 0.46551724137931033, 11.103525386846629, 2.2735176506176464, 'HP:0006265', 'Aplasia/Hypoplasia of fingers'),
(416290, 'HP:0006265', 'Aplasia/Hypoplasia of fingers', 'XPO:0128497', 'decreased size of the digit-joint region', 0.4358974358974359, 6.466375519622663, 1.6788914522843543, 'UPHENO:0086700', 'abnormal digit morphology'),
(416291, 'HP:0006265', 'Aplasia/Hypoplasia of fingers', 'XPO:0141108', 'abnormally necrotic forelimb digit 2', 0.4742268041237113, 7.492661022682715, 1.8849988570736913, 'HP:0001167', 'Abnormal finger morphology'),
(416292, 'HP:0006265', 'Aplasia/Hypoplasia of fingers', 'XPO:0102529', 'abnormal forelimb digit 4 morphology', 0.5227272727272727, 7.492661022682715, 1.9790447852074682, 'HP:0001167', 'Abnormal finger morphology'),
(416293, 'HP:0006265', 'Aplasia/Hypoplasia of fingers', 'XPO:0128172', 'decreased size of the forelimb digit 3', 0.46, 7.492661022682715, 1.8565085699866966, 'HP:0001167', 'Abnormal finger morphology'),
(416294, 'HP:0006265', 'Aplasia/Hypoplasia of fingers', 'XPO:0102787', 'abnormal forelimb digit 5 morphology', 0.5227272727272727, 7.492661022682715, 1.9790447852074682, 'HP:0001167', 'Abnormal finger morphology'),
(416295, 'HP:0006265', 'Aplasia/Hypoplasia of fingers', 'XPO:0102746', 'abnormal forelimb digit 2 morphology', 0.5227272727272727, 7.492661022682715, 1.9790447852074682, 'HP:0001167', 'Abnormal finger morphology'),
(416296, 'HP:0006265', 'Aplasia/Hypoplasia of fingers', 'XPO:0129188', 'decreased size of the forelimb digit 2', 0.46, 7.492661022682715, 1.8565085699866966, 'HP:0001167', 'Abnormal finger morphology'),
(416297, 'HP:0006265', 'Aplasia/Hypoplasia of fingers', 'XPO:0129977', 'increased size of the digit-joint region', 0.4358974358974359, 6.466375519622663, 1.6788914522843543, 'UPHENO:0086700', 'abnormal digit morphology'),
(416298, 'HP:0006265', 'Aplasia/Hypoplasia of fingers', 'XPO:0140716', 'abnormally necrotic forelimb digit 4', 0.4742268041237113, 7.492661022682715, 1.8849988570736913, 'HP:0001167', 'Abnormal finger morphology'),
(416299, 'HP:0006265', 'Aplasia/Hypoplasia of fingers', 'XPO:0102880', 'abnormal digit-joint region morphology', 0.4722222222222222, 6.466375519622663, 1.7474456265073288, 'UPHENO:0086700', 'abnormal digit morphology'),
(416300, 'HP:0006265', 'Aplasia/Hypoplasia of fingers', 'XPO:0101114', 'abnormal forelimb digit 2', 0.4050632911392405, 7.059765001318215, 1.6910504564038238, 'UPHENO:0002708', 'abnormal manus'),
(416301, 'HP:0006265', 'Aplasia/Hypoplasia of fingers', 'XPO:0100966', 'abnormal forelimb digit 3', 0.4050632911392405, 7.059765001318215, 1.6910504564038238, 'UPHENO:0002708', 'abnormal manus'),
(416302, 'HP:0006265', 'Aplasia/Hypoplasia of fingers', 'XPO:0133378', 'fused forelimb digits part of regenerating forelimb', 0.45098039215686275, 7.492661022682715, 1.8382173990874668, 'HP:0001167', 'Abnormal finger morphology'),
(416303, 'HP:0006265', 'Aplasia/Hypoplasia of fingers', 'XPO:0103779', 'decreased size of the forelimb digit in the regenerating forelimb', 0.4423076923076923, 7.492661022682715, 1.820456427983539, 'HP:0001167', 'Abnormal finger morphology'),
(416304, 'HP:0006265', 'Aplasia/Hypoplasia of fingers', 'XPO:0103280', 'absent forelimb digit 3', 0.5346534653465347, 11.103525386846629, 2.4365012467964737, 'HP:0006265', 'Aplasia/Hypoplasia of fingers'),
(416305, 'HP:0006265', 'Aplasia/Hypoplasia of fingers', 'XPO:0130624', 'increased size of the forelimb digit 4', 0.46464646464646464, 7.492661022682715, 1.8658613171894334, 'HP:0001167', 'Abnormal finger morphology'),
(416306, 'HP:0006265', 'Aplasia/Hypoplasia of fingers', 'XPO:0103468', 'bifurcated forelimb digit 5', 0.4380952380952381, 7.492661022682715, 1.8117668488795942, 'HP:0001167', 'Abnormal finger morphology'),
(416307, 'HP:0006265', 'Aplasia/Hypoplasia of fingers', 'XPO:0129652', 'increased size of the forelimb digit 3', 0.46464646464646464, 7.492661022682715, 1.8658613171894334, 'HP:0001167', 'Abnormal finger morphology'),
(416308, 'HP:0006265', 'Aplasia/Hypoplasia of fingers', 'XPO:0140219', 'abnormally necrotic forelimb digit', 0.48936170212765956, 7.492661022682715, 1.914842382945809, 'HP:0001167', 'Abnormal finger morphology'),
(416309, 'HP:0006265', 'Aplasia/Hypoplasia of fingers', 'XPO:0103466', 'bifurcated forelimb digit 3', 0.4380952380952381, 7.492661022682715, 1.8117668488795942, 'HP:0001167', 'Abnormal finger morphology'),
(416310, 'HP:0006265', 'Aplasia/Hypoplasia of fingers', 'XPO:0101155', 'abnormal forelimb digit 5', 0.4050632911392405, 7.059765001318215, 1.6910504564038238, 'UPHENO:0002708', 'abnormal manus'),
(416311, 'HP:0006265', 'Aplasia/Hypoplasia of fingers', 'XPO:0103824', 'decreased length of forelimb digit 5 in regenerating forelimb', 0.46551724137931033, 11.103525386846629, 2.2735176506176464, 'HP:0006265', 'Aplasia/Hypoplasia of fingers'),
(416312, 'HP:0006265', 'Aplasia/Hypoplasia of fingers', 'XPO:0103465', 'bifurcated forelimb digit 2', 0.4380952380952381, 7.492661022682715, 1.8117668488795942, 'HP:0001167', 'Abnormal finger morphology'),
(416313, 'HP:0006265', 'Aplasia/Hypoplasia of fingers', 'XPO:0141568', 'abnormal digit-joint region morphology in the regenerating forelimb', 0.4358974358974359, 6.466375519622663, 1.6788914522843543, 'UPHENO:0086700', 'abnormal digit morphology'),
(416314, 'HP:0006265', 'Aplasia/Hypoplasia of fingers', 'XPO:0103611', 'abnormal number of forelimb digits', 0.4074074074074074, 7.059765001318215, 1.6959364835077422, 'UPHENO:0002708', 'abnormal manus'),
(416315, 'HP:0006265', 'Aplasia/Hypoplasia of fingers', 'XPO:0103432', 'decreased size of the forelimb digit', 0.4742268041237113, 7.492661022682715, 1.8849988570736913, 'HP:0001167', 'Abnormal finger morphology'),
(416316, 'HP:0006265', 'Aplasia/Hypoplasia of fingers', 'XPO:0103281', 'absent forelimb digit 4', 0.5346534653465347, 11.103525386846629, 2.4365012467964737, 'HP:0006265', 'Aplasia/Hypoplasia of fingers'),
(416317, 'HP:0006265', 'Aplasia/Hypoplasia of fingers', 'XPO:0141569', 'abnormal digit-joint region morphology in the regenerating hindlimb', 0.4358974358974359, 6.466375519622663, 1.6788914522843543, 'UPHENO:0086700', 'abnormal digit morphology'),
(416318, 'HP:0006265', 'Aplasia/Hypoplasia of fingers', 'XPO:0102214', 'abnormal forelimb digit morphology', 0.5348837209302325, 7.492661022682715, 2.001924675776152, 'HP:0001167', 'Abnormal finger morphology'),
(416319, 'HP:0006265', 'Aplasia/Hypoplasia of fingers', 'XPO:0103467', 'bifurcated forelimb digit 4', 0.4380952380952381, 7.492661022682715, 1.8117668488795942, 'HP:0001167', 'Abnormal finger morphology'),
(416320, 'HP:0006265', 'Aplasia/Hypoplasia of fingers', 'XPO:0128213', 'decreased size of the digit', 0.41975308641975306, 6.466375519622663, 1.647507536344143, 'UPHENO:0086700', 'abnormal digit morphology'),
(416321, 'HP:0006265', 'Aplasia/Hypoplasia of fingers', 'XPO:0103279', 'absent forelimb digit 2', 0.5346534653465347, 11.103525386846629, 2.4365012467964737, 'HP:0006265', 'Aplasia/Hypoplasia of fingers'),
(416322, 'HP:0006265', 'Aplasia/Hypoplasia of fingers', 'XPO:0129693', 'increased size of the digit', 0.41975308641975306, 6.466375519622663, 1.647507536344143, 'UPHENO:0086700', 'abnormal digit morphology'),
(416323, 'HP:0006265', 'Aplasia/Hypoplasia of fingers', 'XPO:0101248', 'abnormal digit-joint region', 0.4057971014492754, 6.393467666143939, 1.6107298492083872, 'UPHENO:0002905', 'abnormal digit'),
(416324, 'HP:0006265', 'Aplasia/Hypoplasia of fingers', 'XPO:0130664', 'increased size of the forelimb digit 2', 0.46464646464646464, 7.492661022682715, 1.8658613171894334, 'HP:0001167', 'Abnormal finger morphology'),
(416325, 'HP:0006265', 'Aplasia/Hypoplasia of fingers', 'XPO:0125257', 'absent forelimb digit', 0.5510204081632653, 11.103525386846629, 2.473513511325824, 'HP:0006265', 'Aplasia/Hypoplasia of fingers'),
(416326, 'HP:0006265', 'Aplasia/Hypoplasia of fingers', 'XPO:0103823', 'decreased length of forelimb digit 4 in regenerating forelimb', 0.46551724137931033, 11.103525386846629, 2.2735176506176464, 'HP:0006265', 'Aplasia/Hypoplasia of fingers'),
(416327, 'HP:0006265', 'Aplasia/Hypoplasia of fingers', 'XPO:0133358', 'fused forelimb digits', 0.4842105263157895, 7.492661022682715, 1.904737603266917, 'HP:0001167', 'Abnormal finger morphology'),
(416328, 'HP:0006265', 'Aplasia/Hypoplasia of fingers', 'XPO:0103282', 'absent forelimb digit 5', 0.5346534653465347, 11.103525386846629, 2.4365012467964737, 'HP:0006265', 'Aplasia/Hypoplasia of fingers'),
(416329, 'HP:0006265', 'Aplasia/Hypoplasia of fingers', 'XPO:0129148', 'decreased size of the forelimb digit 4', 0.46, 7.492661022682715, 1.8565085699866966, 'HP:0001167', 'Abnormal finger morphology'),
(416330, 'HP:0006265', 'Aplasia/Hypoplasia of fingers', 'XPO:0103822', 'decreased length of forelimb digit 3 in regenerating forelimb', 0.46551724137931033, 11.103525386846629, 2.2735176506176464, 'HP:0006265', 'Aplasia/Hypoplasia of fingers'),
(416331, 'HP:0006265', 'Aplasia/Hypoplasia of fingers', 'XPO:0101810', 'abnormal digit morphology', 0.4722222222222222, 6.466375519622663, 1.7474456265073288, 'UPHENO:0086700', 'abnormal digit morphology'),
(416332, 'HP:0006265', 'Aplasia/Hypoplasia of fingers', 'XPO:0103634', 'abnormally increased number of forelimb digit', 0.42201834862385323, 7.492661022682715, 1.7782127070715896, 'HP:0001167', 'Abnormal finger morphology'),
(416333, 'HP:0009564', 'Triangular shaped distal phalanx of the 2nd finger', 'XPO:0103609', 'abnormally increased number of forelimb digit in the regenerating forelimb', 0.41007194244604317, 7.774297771301195, 1.7855031190763642, 'HP:0005918', 'Abnormal finger phalanx morphology'),
(416334, 'HP:0009564', 'Triangular shaped distal phalanx of the 2nd finger', 'XPO:0103634', 'abnormally increased number of forelimb digit', 0.42857142857142855, 7.774297771301195, 1.8253333673568306, 'HP:0005918', 'Abnormal finger phalanx morphology'),
(416335, 'HP:0011747', 'Abnormality of the anterior pituitary', 'XPO:0128958', 'decreased size of the pars nervosa', 0.5529411764705883, 9.837010412277873, 2.3322281428536003, 'UPHENO:0087940', 'abnormal pituitary gland morphology'),
(416336, 'HP:0011747', 'Abnormality of the anterior pituitary', 'XPO:0125415', 'absent adenohypophysis', 0.40229885057471265, 7.431510076152836, 1.7290714160122713, 'UPHENO:0004618', 'abnormal diencephalon'),
(416337, 'HP:0011747', 'Abnormality of the anterior pituitary', 'XPO:0128214', 'decreased size of the adenohypophysis', 0.5595238095238095, 9.837010412277873, 2.3460693809440283, 'UPHENO:0087940', 'abnormal pituitary gland morphology'),
(416338, 'HP:0011747', 'Abnormality of the anterior pituitary', 'XPO:0100951', 'abnormal adenohypophysis', 0.43661971830985913, 7.431510076152836, 1.801317250255138, 'UPHENO:0004618', 'abnormal diencephalon'),
(416339, 'HP:0011747', 'Abnormality of the anterior pituitary', 'XPO:0100315', 'abnormal neurohypophysis', 0.43661971830985913, 7.431510076152836, 1.801317250255138, 'UPHENO:0004618', 'abnormal diencephalon'),
(416340, 'HP:0011747', 'Abnormality of the anterior pituitary', 'XPO:0100763', 'abnormal pretectum', 0.4142857142857143, 7.431510076152836, 1.7546419749112527, 'UPHENO:0004618', 'abnormal diencephalon'),
(416341, 'HP:0011747', 'Abnormality of the anterior pituitary', 'XPO:0125696', 'absent pars intermedia', 0.40229885057471265, 7.431510076152836, 1.7290714160122713, 'UPHENO:0004618', 'abnormal diencephalon'),
(416342, 'HP:0011747', 'Abnormality of the anterior pituitary', 'XPO:0102546', 'abnormal pars intermedia morphology', 0.6103896103896104, 9.837010412277873, 2.450389551265029, 'UPHENO:0087940', 'abnormal pituitary gland morphology'),
(416343, 'HP:0011747', 'Abnormality of the anterior pituitary', 'XPO:0129694', 'increased size of the adenohypophysis', 0.5595238095238095, 9.837010412277873, 2.3460693809440283, 'UPHENO:0087940', 'abnormal pituitary gland morphology'),
(416344, 'HP:0011747', 'Abnormality of the anterior pituitary', 'XPO:0140252', 'abnormally necrotic infundibulum', 0.5465116279069767, 9.837010412277873, 2.318629029006551, 'UPHENO:0087940', 'abnormal pituitary gland morphology'),
(416345, 'HP:0011747', 'Abnormality of the anterior pituitary', 'XPO:0100946', 'abnormal melanotrope', 0.4189189189189189, 7.431510076152836, 1.7644262996897884, 'UPHENO:0004618', 'abnormal diencephalon'),
(416346, 'HP:0011747', 'Abnormality of the anterior pituitary', 'XPO:0101068', 'abnormal pineal gland', 0.4189189189189189, 7.431510076152836, 1.7644262996897884, 'UPHENO:0004618', 'abnormal diencephalon'),
(416347, 'HP:0011747', 'Abnormality of the anterior pituitary', 'XPO:0102700', 'abnormal pineal gland morphology', 0.4111111111111111, 9.57542522308115, 1.9840775445587429, 'UPHENO:0086771', 'abnormal neuroendocrine gland morphology'),
(416348, 'HP:0011747', 'Abnormality of the anterior pituitary', 'XPO:0100988', 'abnormal habenula', 0.4027777777777778, 7.431510076152836, 1.7301003190584074, 'UPHENO:0004618', 'abnormal diencephalon'),
(416349, 'HP:0011747', 'Abnormality of the anterior pituitary', 'XPO:0100914', 'abnormal pars intermedia', 0.4305555555555556, 7.431510076152836, 1.7887643638709636, 'UPHENO:0004618', 'abnormal diencephalon'),
(416350, 'HP:0011747', 'Abnormality of the anterior pituitary', 'XPO:0102578', 'abnormal melanotrope morphology', 0.5802469135802469, 9.837010412277873, 2.389120116398711, 'UPHENO:0087940', 'abnormal pituitary gland morphology'),
(416351, 'HP:0011747', 'Abnormality of the anterior pituitary', 'XPO:0100698', 'abnormal optic stalk', 0.4027777777777778, 7.431510076152836, 1.7301003190584074, 'UPHENO:0004618', 'abnormal diencephalon'),
(416352, 'HP:0011747', 'Abnormality of the anterior pituitary', 'XPO:0101075', 'abnormal mammilary region', 0.4027777777777778, 7.431510076152836, 1.7301003190584074, 'UPHENO:0004618', 'abnormal diencephalon'),
(416353, 'HP:0011747', 'Abnormality of the anterior pituitary', 'XPO:0125890', 'absent neurohypophysis', 0.40229885057471265, 7.431510076152836, 1.7290714160122713, 'UPHENO:0004618', 'abnormal diencephalon'),
(416354, 'HP:0011747', 'Abnormality of the anterior pituitary', 'XPO:0130794', 'increased size of the pars intermedia', 0.5662650602409639, 9.837010412277873, 2.360160014426886, 'UPHENO:0087940', 'abnormal pituitary gland morphology'),
(416355, 'HP:0011747', 'Abnormality of the anterior pituitary', 'XPO:0101053', 'abnormal anterior hypothalamus', 0.4084507042253521, 7.431510076152836, 1.7422415228843635, 'UPHENO:0004618', 'abnormal diencephalon'),
(416356, 'HP:0011747', 'Abnormality of the anterior pituitary', 'XPO:0130435', 'increased size of the neurohypophysis', 0.5595238095238095, 9.837010412277873, 2.3460693809440283, 'UPHENO:0087940', 'abnormal pituitary gland morphology'),
(416357, 'HP:0011747', 'Abnormality of the anterior pituitary', 'XPO:0100962', 'abnormal dorsal thalamus', 0.4084507042253521, 7.431510076152836, 1.7422415228843635, 'UPHENO:0004618', 'abnormal diencephalon'),
(416358, 'HP:0011747', 'Abnormality of the anterior pituitary', 'XPO:0100263', 'abnormal prethalamus', 0.4084507042253521, 7.431510076152836, 1.7422415228843635, 'UPHENO:0004618', 'abnormal diencephalon'),
(416359, 'HP:0011747', 'Abnormality of the anterior pituitary', 'XPO:0101186', 'abnormal optic chiasm', 0.4142857142857143, 7.431510076152836, 1.7546419749112527, 'UPHENO:0004618', 'abnormal diencephalon'),
(416360, 'HP:0011747', 'Abnormality of the anterior pituitary', 'XPO:0128490', 'decreased size of the infundibulum', 0.5340909090909091, 9.837010412277873, 2.29212954124112, 'UPHENO:0087940', 'abnormal pituitary gland morphology'),
(416361, 'HP:0011747', 'Abnormality of the anterior pituitary', 'XPO:0100611', 'abnormal hypophysis', 0.44285714285714284, 7.431510076152836, 1.814138175398752, 'UPHENO:0004618', 'abnormal diencephalon'),
(416362, 'HP:0011747', 'Abnormality of the anterior pituitary', 'XPO:0100194', 'abnormal preoptic area', 0.4027777777777778, 7.431510076152836, 1.7301003190584074, 'UPHENO:0004618', 'abnormal diencephalon'),
(416363, 'HP:0011747', 'Abnormality of the anterior pituitary', 'XPO:0140405', 'abnormally necrotic adenohypophysis', 0.573170731707317, 9.837010412277873, 2.374507623870221, 'UPHENO:0087940', 'abnormal pituitary gland morphology'),
(416364, 'HP:0011747', 'Abnormality of the anterior pituitary', 'XPO:0100491', 'abnormal pars distalis', 0.4305555555555556, 7.431510076152836, 1.7887643638709636, 'UPHENO:0004618', 'abnormal diencephalon'),
(416365, 'HP:0011747', 'Abnormality of the anterior pituitary', 'XPO:0101595', 'abnormal prosomere 4', 0.4027777777777778, 7.431510076152836, 1.7301003190584074, 'UPHENO:0004618', 'abnormal diencephalon'),
(416366, 'HP:0011747', 'Abnormality of the anterior pituitary', 'XPO:0130518', 'increased size of the pars distalis', 0.5529411764705883, 9.837010412277873, 2.3322281428536003, 'UPHENO:0087940', 'abnormal pituitary gland morphology'),
(416367, 'HP:0011747', 'Abnormality of the anterior pituitary', 'XPO:0129041', 'decreased size of the pars distalis', 0.5529411764705883, 9.837010412277873, 2.3322281428536003, 'UPHENO:0087940', 'abnormal pituitary gland morphology'),
(416368, 'HP:0011747', 'Abnormality of the anterior pituitary', 'XPO:0100195', 'abnormal retromammillary area', 0.4084507042253521, 7.431510076152836, 1.7422415228843635, 'UPHENO:0004618', 'abnormal diencephalon'),
(416369, 'HP:0011747', 'Abnormality of the anterior pituitary', 'XPO:0103158', 'abnormal infundibulum morphology', 0.5802469135802469, 9.837010412277873, 2.389120116398711, 'UPHENO:0087940', 'abnormal pituitary gland morphology'),
(416370, 'HP:0011747', 'Abnormality of the anterior pituitary', 'XPO:0100575', 'abnormal diencephalon', 0.42028985507246375, 7.431510076152836, 1.7673110345595169, 'UPHENO:0004618', 'abnormal diencephalon'),
(416371, 'HP:0011747', 'Abnormality of the anterior pituitary', 'XPO:0140341', 'abnormally necrotic neurohypophysis', 0.573170731707317, 9.837010412277873, 2.374507623870221, 'UPHENO:0087940', 'abnormal pituitary gland morphology'),
(416372, 'HP:0011747', 'Abnormality of the anterior pituitary', 'XPO:0129970', 'increased size of the infundibulum', 0.5340909090909091, 9.837010412277873, 2.29212954124112, 'UPHENO:0087940', 'abnormal pituitary gland morphology'),
(416373, 'HP:0011747', 'Abnormality of the anterior pituitary', 'XPO:0100233', 'abnormal pars nervosa', 0.4305555555555556, 7.431510076152836, 1.7887643638709636, 'UPHENO:0004618', 'abnormal diencephalon'),
(416374, 'HP:0011747', 'Abnormality of the anterior pituitary', 'XPO:0140782', 'abnormally necrotic melanotrope', 0.5529411764705883, 9.837010412277873, 2.3322281428536003, 'UPHENO:0087940', 'abnormal pituitary gland morphology'),
(416375, 'HP:0011747', 'Abnormality of the anterior pituitary', 'XPO:0100590', 'abnormal hypothalamus', 0.4142857142857143, 7.431510076152836, 1.7546419749112527, 'UPHENO:0004618', 'abnormal diencephalon'),
(416376, 'HP:0011747', 'Abnormality of the anterior pituitary', 'XPO:0102243', 'abnormal hypophysis morphology', 0.618421052631579, 9.837010412277873, 2.4664578516383946, 'UPHENO:0087940', 'abnormal pituitary gland morphology'),
(416377, 'HP:0011747', 'Abnormality of the anterior pituitary', 'XPO:0128957', 'decreased size of the neurohypophysis', 0.5595238095238095, 9.837010412277873, 2.3460693809440283, 'UPHENO:0087940', 'abnormal pituitary gland morphology'),
(416378, 'HP:0011747', 'Abnormality of the anterior pituitary', 'XPO:0126921', 'abnormally localised hypophysis', 0.4430379746835443, 7.431510076152836, 1.8145085210544216, 'UPHENO:0004618', 'abnormal diencephalon'),
(416379, 'HP:0011747', 'Abnormality of the anterior pituitary', 'XPO:0141184', 'abnormally necrotic pars intermedia', 0.5802469135802469, 9.837010412277873, 2.389120116398711, 'UPHENO:0087940', 'abnormal pituitary gland morphology'),
(416380, 'HP:0011747', 'Abnormality of the anterior pituitary', 'XPO:0130315', 'increased size of the melanotrope', 0.5053763440860215, 9.837010412277873, 2.2296619382527743, 'UPHENO:0087940', 'abnormal pituitary gland morphology'),
(416381, 'HP:0011747', 'Abnormality of the anterior pituitary', 'XPO:0102583', 'abnormal adenohypophysis morphology', 0.6103896103896104, 9.837010412277873, 2.450389551265029, 'UPHENO:0087940', 'abnormal pituitary gland morphology'),
(416382, 'HP:0011747', 'Abnormality of the anterior pituitary', 'XPO:0140253', 'abnormally necrotic hypophysis', 0.5802469135802469, 9.837010412277873, 2.389120116398711, 'UPHENO:0087940', 'abnormal pituitary gland morphology'),
(416383, 'HP:0011747', 'Abnormality of the anterior pituitary', 'XPO:0101117', 'abnormal tuberal region', 0.4027777777777778, 7.431510076152836, 1.7301003190584074, 'UPHENO:0004618', 'abnormal diencephalon'),
(416384, 'HP:0011747', 'Abnormality of the anterior pituitary', 'XPO:0130436', 'increased size of the pars nervosa', 0.5529411764705883, 9.837010412277873, 2.3322281428536003, 'UPHENO:0087940', 'abnormal pituitary gland morphology'),
(416385, 'HP:0011747', 'Abnormality of the anterior pituitary', 'XPO:0102123', 'abnormal pars distalis morphology', 0.6025641025641025, 9.837010412277873, 2.434631255650011, 'UPHENO:0087940', 'abnormal pituitary gland morphology'),
(416386, 'HP:0011747', 'Abnormality of the anterior pituitary', 'XPO:0100729', 'abnormal thalamus', 0.4142857142857143, 7.431510076152836, 1.7546419749112527, 'UPHENO:0004618', 'abnormal diencephalon'),
(416387, 'HP:0011747', 'Abnormality of the anterior pituitary', 'XPO:0100695', 'abnormal zona limitans intrathalamica', 0.4084507042253521, 7.431510076152836, 1.7422415228843635, 'UPHENO:0004618', 'abnormal diencephalon'),
(416388, 'HP:0011747', 'Abnormality of the anterior pituitary', 'XPO:0140394', 'abnormally necrotic pars nervosa', 0.5662650602409639, 9.837010412277873, 2.360160014426886, 'UPHENO:0087940', 'abnormal pituitary gland morphology'),
(416389, 'HP:0011747', 'Abnormality of the anterior pituitary', 'XPO:0125079', 'absent infundibulum', 0.4069767441860465, 7.431510076152836, 1.739095102396209, 'UPHENO:0004618', 'abnormal diencephalon'),
(416390, 'HP:0011747', 'Abnormality of the anterior pituitary', 'XPO:0128837', 'decreased size of the melanotrope', 0.5053763440860215, 9.837010412277873, 2.2296619382527743, 'UPHENO:0087940', 'abnormal pituitary gland morphology'),
(416391, 'HP:0011747', 'Abnormality of the anterior pituitary', 'XPO:0128489', 'decreased size of the hypophysis', 0.5402298850574713, 9.837010412277873, 2.3052650616217703, 'UPHENO:0087940', 'abnormal pituitary gland morphology'),
(416392, 'HP:0011747', 'Abnormality of the anterior pituitary', 'XPO:0101293', 'abnormal posterior hypothalamus', 0.4084507042253521, 7.431510076152836, 1.7422415228843635, 'UPHENO:0004618', 'abnormal diencephalon'),
(416393, 'HP:0011747', 'Abnormality of the anterior pituitary', 'XPO:0101947', 'abnormal neurohypophysis morphology', 0.6103896103896104, 9.837010412277873, 2.450389551265029, 'UPHENO:0087940', 'abnormal pituitary gland morphology'),
(416394, 'HP:0011747', 'Abnormality of the anterior pituitary', 'XPO:0129969', 'increased size of the hypophysis', 0.5402298850574713, 9.837010412277873, 2.3052650616217703, 'UPHENO:0087940', 'abnormal pituitary gland morphology'),
(416395, 'HP:0011747', 'Abnormality of the anterior pituitary', 'XPO:0101865', 'abnormal pars nervosa morphology', 0.6025641025641025, 9.837010412277873, 2.434631255650011, 'UPHENO:0087940', 'abnormal pituitary gland morphology'),
(416396, 'HP:0011747', 'Abnormality of the anterior pituitary', 'XPO:0140316', 'abnormally necrotic pars distalis', 0.5662650602409639, 9.837010412277873, 2.360160014426886, 'UPHENO:0087940', 'abnormal pituitary gland morphology'),
(416397, 'HP:0011747', 'Abnormality of the anterior pituitary', 'XPO:0101123', 'abnormal third ventricle', 0.4027777777777778, 7.431510076152836, 1.7301003190584074, 'UPHENO:0004618', 'abnormal diencephalon'),
(416398, 'HP:0011747', 'Abnormality of the anterior pituitary', 'XPO:0101496', 'abnormal subcommissural organ', 0.4084507042253521, 7.431510076152836, 1.7422415228843635, 'UPHENO:0004618', 'abnormal diencephalon'),
(416399, 'HP:0011747', 'Abnormality of the anterior pituitary', 'XPO:0101354', 'abnormal eminentia thalami', 0.4142857142857143, 7.431510076152836, 1.7546419749112527, 'UPHENO:0004618', 'abnormal diencephalon'),
(416400, 'HP:0011747', 'Abnormality of the anterior pituitary', 'XPO:0100157', 'abnormal optic tract', 0.4142857142857143, 7.431510076152836, 1.7546419749112527, 'UPHENO:0004618', 'abnormal diencephalon'),
(416401, 'HP:0011747', 'Abnormality of the anterior pituitary', 'XPO:0101526', 'abnormal infundibulum', 0.44285714285714284, 7.431510076152836, 1.814138175398752, 'UPHENO:0004618', 'abnormal diencephalon'),
(416402, 'HP:0011747', 'Abnormality of the anterior pituitary', 'XPO:0129318', 'decreased size of the pars intermedia', 0.5662650602409639, 9.837010412277873, 2.360160014426886, 'UPHENO:0087940', 'abnormal pituitary gland morphology'),
(416403, 'HP:0010497', 'Sirenomelia', 'XPO:0115391', 'abnormally undifferentiated alimentary system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(416404, 'HP:0010497', 'Sirenomelia', 'XPO:0100458', 'abnormal autopod', 0.52, 5.504475013697824, 1.6918413067196547, 'HP:0040064', 'Abnormality of limbs'),
(416405, 'HP:0010497', 'Sirenomelia', 'XPO:0100956', 'abnormal centrosome', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(416406, 'HP:0010497', 'Sirenomelia', 'XPO:0101575', 'abnormal vitelline membrane', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(416407, 'HP:0010497', 'Sirenomelia', 'XPO:0100070', 'abnormal anatomical system', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416408, 'HP:0010497', 'Sirenomelia', 'XPO:0100437', 'abnormal proepicardium', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(416409, 'HP:0010497', 'Sirenomelia', 'XPO:0101212', 'abnormal glomeral mesenchyme', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(416410, 'HP:0010497', 'Sirenomelia', 'XPO:0100728', 'abnormal cell condensation', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416411, 'HP:0010497', 'Sirenomelia', 'XPO:0100551', 'abnormal oocyte cortex', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(416412, 'HP:0010497', 'Sirenomelia', 'XPO:0100025', 'abnormal oocyte', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(416413, 'HP:0010497', 'Sirenomelia', 'XPO:0141266', 'abnormal surface breathing', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(416414, 'HP:0010497', 'Sirenomelia', 'XPO:0141271', 'increased surface breathing', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(416415, 'HP:0010497', 'Sirenomelia', 'XPO:0131685', 'abnormal cortical actin cytoskeleton', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(416416, 'HP:0010497', 'Sirenomelia', 'XPO:0141662', 'paralysed forelimb', 0.43333333333333335, 5.504475013697824, 1.5444327456822857, 'HP:0040064', 'Abnormality of limbs'),
(416417, 'HP:0010497', 'Sirenomelia', 'XPO:0107265', 'abnormal posterior side', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416418, 'HP:0010497', 'Sirenomelia', 'XPO:0100585', 'abnormal elastica externa', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(416419, 'HP:0010497', 'Sirenomelia', 'XPO:0100784', 'abnormal left blastomere', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(416420, 'HP:0010497', 'Sirenomelia', 'XPO:0115509', 'abnormally semi-viable whole organism', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416421, 'HP:0010497', 'Sirenomelia', 'XPO:0100403', 'abnormal forelimb', 0.5, 5.504475013697824, 1.6589868917049684, 'HP:0040064', 'Abnormality of limbs'),
(416422, 'HP:0010497', 'Sirenomelia', 'XPO:0100172', 'abnormal stem cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(416423, 'HP:0010497', 'Sirenomelia', 'XPO:0107288', 'abnormal larval alimentary system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(416424, 'HP:0010497', 'Sirenomelia', 'XPO:0131669', 'abnormal Roux spot', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(416425, 'HP:0010497', 'Sirenomelia', 'XPO:0107262', 'abnormal left-right axis', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416426, 'HP:0010497', 'Sirenomelia', 'XPO:0100515', 'abnormal somatic stem cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(416427, 'HP:0010497', 'Sirenomelia', 'XPO:0101220', 'abnormal centriole', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(416428, 'HP:0010497', 'Sirenomelia', 'XPO:0141714', 'abnormal anterior notochord', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(416429, 'HP:0010497', 'Sirenomelia', 'XPO:0100277', 'abnormal blastocoel', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416430, 'HP:0010497', 'Sirenomelia', 'XPO:0101333', 'abnormal barrier epithelial cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(416431, 'HP:0010497', 'Sirenomelia', 'XPO:0100339', 'abnormal circumblastoporal collar', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416432, 'HP:0010497', 'Sirenomelia', 'XPO:0100026', 'abnormal germ cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(416433, 'HP:0010497', 'Sirenomelia', 'XPO:0141715', 'abnormal septum', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416434, 'HP:0010497', 'Sirenomelia', 'XPO:0100225', 'abnormal endocrine system', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(416435, 'HP:0010497', 'Sirenomelia', 'XPO:0101221', 'abnormal larval immune system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(416436, 'HP:0010497', 'Sirenomelia', 'XPO:0115508', 'abnormally peramorphic growth of whole organism', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416437, 'HP:0010497', 'Sirenomelia', 'XPO:0100557', 'abnormal prime meridian', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416438, 'HP:0010497', 'Sirenomelia', 'XPO:0131723', 'abnormal pathway-restricted SMAD protein phosphorylation', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(416439, 'HP:0010497', 'Sirenomelia', 'XPO:0101283', 'abnormal left-ventral blastomere', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(416440, 'HP:0010497', 'Sirenomelia', 'XPO:0100626', 'abnormal primordial germ cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(416441, 'HP:0010497', 'Sirenomelia', 'XPO:0131666', 'abnormal adherens junction', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(416442, 'HP:0010497', 'Sirenomelia', 'XPO:0100176', 'abnormal stage VI oocyte', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(416443, 'HP:0010497', 'Sirenomelia', 'XPO:0131691', 'abnormal molecular function', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(416444, 'HP:0010497', 'Sirenomelia', 'XPO:0141745', 'abnormal creatinine homeostasis', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(416445, 'HP:0010497', 'Sirenomelia', 'XPO:0141663', 'paralysed hindlimb', 0.43333333333333335, 5.504475013697824, 1.5444327456822857, 'HP:0040064', 'Abnormality of limbs'),
(416446, 'HP:0010497', 'Sirenomelia', 'XPO:0100665', 'abnormal egg jelly', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416447, 'HP:0010497', 'Sirenomelia', 'XPO:0107272', 'abnormal axial region', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416448, 'HP:0010497', 'Sirenomelia', 'XPO:0141791', 'abnormal primary metabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(416449, 'HP:0010497', 'Sirenomelia', 'XPO:0101497', 'abnormal ciliary axoneme', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(416450, 'HP:0010497', 'Sirenomelia', 'XPO:0100545', 'abnormal male organism', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416451, 'HP:0010497', 'Sirenomelia', 'XPO:0101547', 'abnormal lampbrush chromosome', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(416452, 'HP:0010497', 'Sirenomelia', 'XPO:0100691', 'abnormal keratin accumulating cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(416453, 'HP:0010497', 'Sirenomelia', 'XPO:0142057', 'abnormal desmosome', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(416454, 'HP:0010497', 'Sirenomelia', 'XPO:0101448', 'abnormal myelin accumulating cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(416455, 'HP:0010497', 'Sirenomelia', 'XPO:0141792', 'abnormal small molecule metabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(416456, 'HP:0010497', 'Sirenomelia', 'XPO:0101302', 'abnormal subcortical cytoplasm', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(416457, 'HP:0010497', 'Sirenomelia', 'XPO:0101004', 'abnormal acid secreting cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(416458, 'HP:0010497', 'Sirenomelia', 'XPO:0100162', 'abnormal presumptive rhombomere', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416459, 'HP:0010497', 'Sirenomelia', 'XPO:0142051', 'abnormal cerebrospinal fluid', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(416460, 'HP:0010497', 'Sirenomelia', 'XPO:0101061', 'abnormal plasma membrane', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(416461, 'HP:0010497', 'Sirenomelia', 'XPO:0141796', 'abnormal demethylation', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(416462, 'HP:0010497', 'Sirenomelia', 'XPO:0100308', 'abnormal early embryonic cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(416463, 'HP:0010497', 'Sirenomelia', 'XPO:0100003', 'abnormal organism subdivision', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416464, 'HP:0010497', 'Sirenomelia', 'XPO:0102484', 'abnormal interdigital region morphology', 0.41935483870967744, 5.504475013697824, 1.5193183443737854, 'HP:0040064', 'Abnormality of limbs'),
(416465, 'HP:0010497', 'Sirenomelia', 'XPO:0142052', 'abnormal nasal region', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(416466, 'HP:0010497', 'Sirenomelia', 'XPO:0100643', 'abnormal thoracic region', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416467, 'HP:0010497', 'Sirenomelia', 'XPO:0100151', 'abnormal primordium', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416468, 'HP:0010497', 'Sirenomelia', 'XPO:0100852', 'abnormal interdigital region', 0.6190476190476191, 5.504475013697824, 1.8459502028323378, 'HP:0040064', 'Abnormality of limbs'),
(416469, 'HP:0010497', 'Sirenomelia', 'XPO:0100152', 'abnormal alimentary system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(416470, 'HP:0010497', 'Sirenomelia', 'XPO:0101513', 'abnormal basal body', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(416471, 'HP:0010497', 'Sirenomelia', 'XPO:0100688', 'abnormal adipose tissue', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(416472, 'HP:0010497', 'Sirenomelia', 'XPO:0100969', 'abnormal disaggregated/reaggregated ectoderm treated with activin', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416473, 'HP:0010497', 'Sirenomelia', 'XPO:0107312', 'abnormal filopodium', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(416474, 'HP:0010497', 'Sirenomelia', 'XPO:0100547', 'abnormal blastomere V2', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(416475, 'HP:0010497', 'Sirenomelia', 'XPO:0107285', 'abnormal flexural organ', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(416476, 'HP:0010497', 'Sirenomelia', 'XPO:0101389', 'abnormal wedge region', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(416477, 'HP:0010497', 'Sirenomelia', 'XPO:0141782', 'abnormal methylation', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(416478, 'HP:0010497', 'Sirenomelia', 'XPO:0141264', 'abnormal schooling behavior', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(416479, 'HP:0010497', 'Sirenomelia', 'XPO:0101347', 'abnormal hindlimb region', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416480, 'HP:0010497', 'Sirenomelia', 'XPO:0100503', 'abnormal blastomere D2', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(416481, 'HP:0010497', 'Sirenomelia', 'XPO:0115566', 'abnormal variability of size of forelimb', 0.48148148148148145, 5.504475013697824, 1.6279750564345348, 'HP:0040064', 'Abnormality of limbs'),
(416482, 'HP:0010497', 'Sirenomelia', 'XPO:0100581', 'abnormal immune system', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(416483, 'HP:0010497', 'Sirenomelia', 'XPO:0101109', 'abnormal egg cell-free extract', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416484, 'HP:0010497', 'Sirenomelia', 'XPO:0101378', 'abnormal blastomere D1', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(416485, 'HP:0010497', 'Sirenomelia', 'XPO:0100377', 'abnormal connective tissue', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(416486, 'HP:0010497', 'Sirenomelia', 'XPO:0100481', 'abnormal anatomical line', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416487, 'HP:0010497', 'Sirenomelia', 'XPO:0100114', 'abnormal peripheral nervous system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(416488, 'HP:0010497', 'Sirenomelia', 'XPO:0101023', 'abnormal ultimobranchial body', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(416489, 'HP:0010497', 'Sirenomelia', 'XPO:0107269', 'abnormal right side', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416490, 'HP:0010497', 'Sirenomelia', 'XPO:0100902', 'abnormal spermatocyte', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(416491, 'HP:0010497', 'Sirenomelia', 'XPO:0101241', 'abnormal nucleate erythrocyte', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(416492, 'HP:0010497', 'Sirenomelia', 'XPO:0100546', 'abnormal whole organism', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416493, 'HP:0010497', 'Sirenomelia', 'XPO:0101411', 'abnormal marginal zone (sensu neural)', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416494, 'HP:0010497', 'Sirenomelia', 'XPO:0101480', 'abnormal stage V oocyte', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(416495, 'HP:0010497', 'Sirenomelia', 'XPO:0101200', 'abnormal joint region', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416496, 'HP:0010497', 'Sirenomelia', 'XPO:0100231', 'abnormal compound organ', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416497, 'HP:0010497', 'Sirenomelia', 'XPO:0100108', 'abnormal cell part', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(416498, 'HP:0010497', 'Sirenomelia', 'XPO:0141841', 'abnormality of whole organism mass', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(416499, 'HP:0010497', 'Sirenomelia', 'XPO:0100754', 'abnormal electrically active cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(416500, 'HP:0010497', 'Sirenomelia', 'XPO:0107278', 'abnormal medial region', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416501, 'HP:0010497', 'Sirenomelia', 'XPO:0100724', 'abnormal kinetochore', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(416502, 'HP:0010497', 'Sirenomelia', 'XPO:0100715', 'abnormal ciliated cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(416503, 'HP:0010497', 'Sirenomelia', 'XPO:0100745', 'abnormal anterior lymph sac', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(416504, 'HP:0010497', 'Sirenomelia', 'XPO:0100894', 'abnormal nucleus', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(416505, 'HP:0010497', 'Sirenomelia', 'XPO:0100384', 'abnormal amputated tissue', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416506, 'HP:0010497', 'Sirenomelia', 'XPO:0100004', 'abnormal cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(416507, 'HP:0010497', 'Sirenomelia', 'XPO:0100915', 'abnormal dermal system', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416508, 'HP:0010497', 'Sirenomelia', 'XPO:0100307', 'abnormal blastomere', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(416509, 'HP:0010497', 'Sirenomelia', 'XPO:0101168', 'abnormal circulating cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(416510, 'HP:0010497', 'Sirenomelia', 'XPO:0100423', 'abnormal process', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416511, 'HP:0010497', 'Sirenomelia', 'XPO:0125566', 'absent interdigital region', 0.41935483870967744, 5.504475013697824, 1.5193183443737854, 'HP:0040064', 'Abnormality of limbs'),
(416512, 'HP:0010497', 'Sirenomelia', 'XPO:0100120', 'abnormal genital system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(416513, 'HP:0010497', 'Sirenomelia', 'XPO:0100394', 'abnormal marginal zone', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416514, 'HP:0010497', 'Sirenomelia', 'XPO:0116494', 'absent biological process', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(416515, 'HP:0010497', 'Sirenomelia', 'XPO:0100781', 'abnormal presumptive ectoderm', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416516, 'HP:0010497', 'Sirenomelia', 'XPO:0100258', 'abnormal organ part', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416517, 'HP:0010497', 'Sirenomelia', 'XPO:0101405', 'abnormal ring structure', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(416518, 'HP:0010497', 'Sirenomelia', 'XPO:0101136', 'abnormal ooplasm', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(416519, 'HP:0010497', 'Sirenomelia', 'XPO:0107260', 'abnormal anterior-posterior axis', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416520, 'HP:0010497', 'Sirenomelia', 'XPO:0100653', 'abnormal myoblast', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(416521, 'HP:0010497', 'Sirenomelia', 'XPO:0101228', 'abnormal mesenchymal stem cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(416522, 'HP:0010497', 'Sirenomelia', 'XPO:0141797', 'abnormal hydrogen metabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(416523, 'HP:0010497', 'Sirenomelia', 'XPO:0100251', 'abnormal proteinaceous extracellular matrix', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416524, 'HP:0010497', 'Sirenomelia', 'XPO:0100273', 'abnormal visual system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(416525, 'HP:0010497', 'Sirenomelia', 'XPO:0101435', 'abnormal paracrine cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(416526, 'HP:0010497', 'Sirenomelia', 'XPO:0100742', 'abnormal musculoskeletal system', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416527, 'HP:0010497', 'Sirenomelia', 'XPO:0107273', 'abnormal basal region', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416528, 'HP:0010497', 'Sirenomelia', 'XPO:0101132', 'abnormal apoptotic cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(416529, 'HP:0010497', 'Sirenomelia', 'XPO:0100164', 'abnormal neural nucleus', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(416530, 'HP:0010497', 'Sirenomelia', 'XPO:0100862', 'abnormal blastomere V1', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(416531, 'HP:0010497', 'Sirenomelia', 'XPO:0100009', 'abnormal multi-tissue structure', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416532, 'HP:0010497', 'Sirenomelia', 'XPO:0141748', 'abnormal gas homeostasis', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(416533, 'HP:0010497', 'Sirenomelia', 'XPO:0115758', 'abnormally decreased mobility of melanoblast', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(416534, 'HP:0010497', 'Sirenomelia', 'XPO:0100501', 'abnormal urogenital system', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(416535, 'HP:0010497', 'Sirenomelia', 'XPO:0100265', 'abnormal sensory epithelial cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(416536, 'HP:0010497', 'Sirenomelia', 'XPO:0100912', 'abnormal trabecula', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416537, 'HP:0010497', 'Sirenomelia', 'XPO:0101071', 'abnormal endoplasmic reticulum', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(416538, 'HP:0010497', 'Sirenomelia', 'XPO:0101311', 'abnormal bottle cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(416539, 'HP:0010497', 'Sirenomelia', 'XPO:0100999', 'abnormal serous membrane', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416540, 'HP:0010497', 'Sirenomelia', 'XPO:0107261', 'abnormal dorsal-ventral axis', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416541, 'HP:0010497', 'Sirenomelia', 'XPO:0107268', 'abnormal left side', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416542, 'HP:0010497', 'Sirenomelia', 'XPO:0100285', 'abnormal progenitor cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(416543, 'HP:0010497', 'Sirenomelia', 'XPO:0100610', 'abnormal appendage', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416544, 'HP:0010497', 'Sirenomelia', 'XPO:0101519', 'abnormal hypobranchial placode', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416545, 'HP:0010497', 'Sirenomelia', 'XPO:0100427', 'abnormal olfactory system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(416546, 'HP:0010497', 'Sirenomelia', 'XPO:0100846', 'abnormal hindlimb', 0.5, 5.504475013697824, 1.6589868917049684, 'HP:0040064', 'Abnormality of limbs'),
(416547, 'HP:0010497', 'Sirenomelia', 'XPO:0101096', 'abnormal tendon', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(416548, 'HP:0010497', 'Sirenomelia', 'XPO:0141783', 'abnormal collagen metabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(416549, 'HP:0010497', 'Sirenomelia', 'XPO:0101078', 'abnormal mucous gland', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416550, 'HP:0010497', 'Sirenomelia', 'XPO:0141718', 'abnormal posterior notochord', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(416551, 'HP:0010497', 'Sirenomelia', 'XPO:0100493', 'abnormal liver and biliary system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(416552, 'HP:0010497', 'Sirenomelia', 'XPO:0131667', 'abnormal actin cytoskeleton', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(416553, 'HP:0010497', 'Sirenomelia', 'XPO:0141781', 'abnormal secondary metabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(416554, 'HP:0010497', 'Sirenomelia', 'XPO:0100031', 'abnormal central nervous system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(416555, 'HP:0010497', 'Sirenomelia', 'XPO:0101467', 'abnormal alkali secreting cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(416556, 'HP:0010497', 'Sirenomelia', 'XPO:0141743', 'abnormal chemical homeostasis within a tissue', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(416557, 'HP:0010497', 'Sirenomelia', 'XPO:0100457', 'abnormal foot', 0.4482758620689655, 5.504475013697824, 1.570835217966058, 'HP:0040064', 'Abnormality of limbs'),
(416558, 'HP:0010497', 'Sirenomelia', 'XPO:0100822', 'abnormal hindlimb zeugopod', 0.4482758620689655, 5.504475013697824, 1.570835217966058, 'HP:0040064', 'Abnormality of limbs'),
(416559, 'HP:0010497', 'Sirenomelia', 'XPO:0100670', 'abnormal forelimb zeugopod', 0.4482758620689655, 5.504475013697824, 1.570835217966058, 'HP:0040064', 'Abnormality of limbs'),
(416560, 'HP:0010497', 'Sirenomelia', 'XPO:0141777', 'abnormal catabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(416561, 'HP:0010497', 'Sirenomelia', 'XPO:0107276', 'abnormal dorsal region', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416562, 'HP:0010497', 'Sirenomelia', 'XPO:0101362', 'abnormal vegetal cortex', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(416563, 'HP:0010497', 'Sirenomelia', 'XPO:0107253', 'abnormal enteric nervous system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(416564, 'HP:0010497', 'Sirenomelia', 'XPO:0107339', 'abnormal yolk platelet', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(416565, 'HP:0010497', 'Sirenomelia', 'XPO:0100032', 'abnormal nervous system', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(416566, 'HP:0010497', 'Sirenomelia', 'XPO:0101072', 'abnormal mitochondrial cloud', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(416567, 'HP:0010497', 'Sirenomelia', 'XPO:0141499', 'abnormal tadpole', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416568, 'HP:0010497', 'Sirenomelia', 'XPO:0141778', 'abnormal biosynthetic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(416569, 'HP:0010497', 'Sirenomelia', 'XPO:0100317', 'abnormal respiratory system', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(416570, 'HP:0010497', 'Sirenomelia', 'XPO:0100587', 'abnormal vestibuloauditory system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(416571, 'HP:0010497', 'Sirenomelia', 'XPO:0100274', 'abnormal sensory system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(416572, 'HP:0010497', 'Sirenomelia', 'XPO:0100991', 'abnormal iliac process primordium', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416573, 'HP:0010497', 'Sirenomelia', 'XPO:0100856', 'abnormal simple organ', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416574, 'HP:0010497', 'Sirenomelia', 'XPO:0107258', 'abnormal anatomical axis', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416575, 'HP:0010497', 'Sirenomelia', 'XPO:0131675', 'abnormal spindle microtubule', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(416576, 'HP:0010497', 'Sirenomelia', 'XPO:0100135', 'abnormal surface structure', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416577, 'HP:0010497', 'Sirenomelia', 'XPO:0100511', 'abnormal stylopod', 0.52, 5.504475013697824, 1.6918413067196547, 'HP:0040064', 'Abnormality of limbs'),
(416578, 'HP:0010497', 'Sirenomelia', 'XPO:0141787', 'abnormal hormone metabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(416579, 'HP:0010497', 'Sirenomelia', 'XPO:0100791', 'abnormal multiciliated cell precursor', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(416580, 'HP:0010497', 'Sirenomelia', 'XPO:0100023', 'abnormal mesenchyme', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416581, 'HP:0010497', 'Sirenomelia', 'XPO:0101373', 'abnormal oxygen accumulating cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(416582, 'HP:0010497', 'Sirenomelia', 'XPO:0100900', 'abnormal angioblast', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(416583, 'HP:0010497', 'Sirenomelia', 'XPO:0100205', 'abnormal limb segment', 0.5416666666666666, 5.504475013697824, 1.7267283030111178, 'HP:0040064', 'Abnormality of limbs'),
(416584, 'HP:0010497', 'Sirenomelia', 'XPO:0101535', 'abnormal absorptive cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(416585, 'HP:0010497', 'Sirenomelia', 'XPO:0107263', 'abnormal anatomical side', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416586, 'HP:0010497', 'Sirenomelia', 'XPO:0100917', 'abnormal stage III oocyte', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(416587, 'HP:0010497', 'Sirenomelia', 'XPO:0100807', 'abnormal matrix-based tissue', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416588, 'HP:0010497', 'Sirenomelia', 'XPO:0100989', 'abnormal right blastomere', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(416589, 'HP:0010497', 'Sirenomelia', 'XPO:0100014', 'abnormal tissue', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416590, 'HP:0010497', 'Sirenomelia', 'XPO:0100907', 'abnormal cytoplasm', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(416591, 'HP:0010497', 'Sirenomelia', 'XPO:0100363', 'abnormal cardiovascular system', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416592, 'HP:0010497', 'Sirenomelia', 'XPO:0100341', 'abnormal hand', 0.4482758620689655, 5.504475013697824, 1.570835217966058, 'HP:0040064', 'Abnormality of limbs'),
(416593, 'HP:0010497', 'Sirenomelia', 'XPO:0116434', 'abnormal biological process', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(416594, 'HP:0010497', 'Sirenomelia', 'XPO:0100762', 'abnormal intersomitic region', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416595, 'HP:0010497', 'Sirenomelia', 'XPO:0100372', 'abnormal hematological system', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(416596, 'HP:0010497', 'Sirenomelia', 'XPO:0101409', 'abnormal perivitelline space', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(416597, 'HP:0010497', 'Sirenomelia', 'XPO:0100477', 'abnormal pericyte', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(416598, 'HP:0010497', 'Sirenomelia', 'XPO:0141794', 'abnormal prosthetic group metabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(416599, 'HP:0010497', 'Sirenomelia', 'XPO:0107267', 'abnormal ventral side', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416600, 'HP:0010497', 'Sirenomelia', 'XPO:0101240', 'abnormal ciliated non-epidermal cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(416601, 'HP:0010497', 'Sirenomelia', 'XPO:00000000', 'Xenopus phenotype', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(416602, 'HP:0010497', 'Sirenomelia', 'XPO:0101441', 'abnormal interdigital webbing', 0.4482758620689655, 5.504475013697824, 1.570835217966058, 'HP:0040064', 'Abnormality of limbs'),
(416603, 'HP:0010497', 'Sirenomelia', 'XPO:0142056', 'abnormal main body axis', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416604, 'HP:0010497', 'Sirenomelia', 'XPO:0100069', 'abnormal urinary system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(416605, 'HP:0010497', 'Sirenomelia', 'XPO:0100599', 'abnormal adult immune system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(416606, 'HP:0010497', 'Sirenomelia', 'XPO:0100640', 'abnormal notochordal sheath', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(416607, 'HP:0010497', 'Sirenomelia', 'XPO:0101074', 'abnormal germinal vesicle', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(416608, 'HP:0010497', 'Sirenomelia', 'XPO:0100028', 'abnormal anatomical cluster', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416609, 'HP:0010497', 'Sirenomelia', 'XPO:0141267', 'abnormal resting posture', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(416610, 'HP:0010497', 'Sirenomelia', 'XPO:0101176', 'abnormal non-ciliated epithelial cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(416611, 'HP:0010497', 'Sirenomelia', 'XPO:0141770', 'abnormal urate homeostasis', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(416612, 'HP:0010497', 'Sirenomelia', 'XPO:0101297', 'abnormal barrier cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(416613, 'HP:0010497', 'Sirenomelia', 'XPO:0100642', 'abnormal gustatory system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(416614, 'HP:0010497', 'Sirenomelia', 'XPO:0101472', 'abnormal zygote cortex', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(416615, 'HP:0010497', 'Sirenomelia', 'XPO:0100574', 'abnormal gastrula cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(416616, 'HP:0010497', 'Sirenomelia', 'XPO:0101237', 'abnormal mucus secreting cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(416617, 'HP:0010497', 'Sirenomelia', 'XPO:0100293', 'abnormal duct', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416618, 'HP:0010497', 'Sirenomelia', 'XPO:0127203', 'abnormally localised interdigital region', 0.4482758620689655, 5.504475013697824, 1.570835217966058, 'HP:0040064', 'Abnormality of limbs'),
(416619, 'HP:0010497', 'Sirenomelia', 'XPO:0100289', 'abnormal chondroblast', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(416620, 'HP:0010497', 'Sirenomelia', 'XPO:0100429', 'abnormal spermatid', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(416621, 'HP:0010497', 'Sirenomelia', 'XPO:0131687', 'abnormal astral microtubule', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(416622, 'HP:0010497', 'Sirenomelia', 'XPO:0101264', 'abnormal mitotic spindle', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(416623, 'HP:0010497', 'Sirenomelia', 'XPO:0141904', 'abnormal glucosamine metabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(416624, 'HP:0010497', 'Sirenomelia', 'XPO:0141265', 'abnormal escape behavior', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(416625, 'HP:0010497', 'Sirenomelia', 'XPO:0101461', 'abnormal sperm entry point', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(416626, 'HP:0010497', 'Sirenomelia', 'XPO:0100010', 'abnormal multicellular anatomical structure', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416627, 'HP:0010497', 'Sirenomelia', 'XPO:0100674', 'abnormal secondary oogonium', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(416628, 'HP:0010497', 'Sirenomelia', 'XPO:0101463', 'abnormal right-ventral blastomere', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(416629, 'HP:0010497', 'Sirenomelia', 'XPO:0101406', 'abnormal cleavage furrow', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416630, 'HP:0010497', 'Sirenomelia', 'XPO:0100084', 'abnormal anatomical group', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416631, 'HP:0010497', 'Sirenomelia', 'XPO:0101113', 'abnormal stage IV oocyte', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(416632, 'HP:0010497', 'Sirenomelia', 'XPO:0101174', 'abnormal articular system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(416633, 'HP:0010497', 'Sirenomelia', 'XPO:0107284', 'abnormal migrating myoblast', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(416634, 'HP:0010497', 'Sirenomelia', 'XPO:0100337', 'abnormal zygote', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(416635, 'HP:0010497', 'Sirenomelia', 'XPO:0115574', 'abnormal variability of size of hindlimb', 0.48148148148148145, 5.504475013697824, 1.6279750564345348, 'HP:0040064', 'Abnormality of limbs'),
(416636, 'HP:0010497', 'Sirenomelia', 'XPO:0101498', 'abnormal stage II oocyte', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(416637, 'HP:0010497', 'Sirenomelia', 'XPO:0101468', 'abnormal stage I oocyte', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(416638, 'HP:0010497', 'Sirenomelia', 'XPO:0100062', 'abnormal anatomical space', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416639, 'HP:0010497', 'Sirenomelia', 'XPO:0100202', 'abnormal embryo', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416640, 'HP:0010497', 'Sirenomelia', 'XPO:0101451', 'abnormal dorsal lymph space', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(416641, 'HP:0010497', 'Sirenomelia', 'XPO:0100416', 'abnormal ligament', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(416642, 'HP:0010497', 'Sirenomelia', 'XPO:0100667', 'abnormal vegetal yolk mass', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416643, 'HP:0010497', 'Sirenomelia', 'XPO:0100295', 'abnormal extracellular matrix', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416644, 'HP:0010497', 'Sirenomelia', 'XPO:0100417', 'abnormal dense regular connective tissue', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(416645, 'HP:0010497', 'Sirenomelia', 'XPO:0131677', 'abnormal actin filament', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(416646, 'HP:0010497', 'Sirenomelia', 'XPO:0100104', 'abnormal embryonic structure', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416647, 'HP:0010497', 'Sirenomelia', 'XPO:0141775', 'abnormal nitrogen compound metabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(416648, 'HP:0010497', 'Sirenomelia', 'XPO:0141738', 'abnormal carbon dioxide homeostasis', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(416649, 'HP:0010497', 'Sirenomelia', 'XPO:0100786', 'abnormal presumptive axial mesoderm', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416650, 'HP:0010497', 'Sirenomelia', 'XPO:0115512', 'abnormally semi-erect whole organism', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416651, 'HP:0010497', 'Sirenomelia', 'XPO:0141784', 'abnormal cellular hormone metabolic process', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(416652, 'HP:0010497', 'Sirenomelia', 'XPO:0101366', 'abnormal morula cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(416653, 'HP:0010497', 'Sirenomelia', 'XPO:0141263', 'abnormal visually guided collision avoidance behavior', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(416654, 'HP:0010497', 'Sirenomelia', 'XPO:0100704', 'abnormal Merkel cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(416655, 'HP:0010497', 'Sirenomelia', 'XPO:0100888', 'abnormal microtubule', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(416656, 'HP:0010497', 'Sirenomelia', 'XPO:0100060', 'abnormal regenerating tissue', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416657, 'HP:0010497', 'Sirenomelia', 'XPO:0100232', 'abnormal lymphatic system', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(416658, 'HP:0010497', 'Sirenomelia', 'XPO:0101570', 'abnormal forelimb region', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416659, 'HP:0010497', 'Sirenomelia', 'XPO:0100239', 'abnormal acellular anatomical structure', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416660, 'HP:0010497', 'Sirenomelia', 'XPO:0100898', 'abnormal hindlimb stylopod', 0.4482758620689655, 5.504475013697824, 1.570835217966058, 'HP:0040064', 'Abnormality of limbs'),
(416661, 'HP:0010497', 'Sirenomelia', 'XPO:0141276', 'decreased surface breathing', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(416662, 'HP:0010497', 'Sirenomelia', 'XPO:0101110', 'abnormal cell-free extract', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416663, 'HP:0010497', 'Sirenomelia', 'XPO:0100465', 'abnormal skeletal system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(416664, 'HP:0010497', 'Sirenomelia', 'XPO:0141771', 'abnormal urea homeostasis', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(416665, 'HP:0010497', 'Sirenomelia', 'XPO:0107271', 'abnormal apical region', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416666, 'HP:0010497', 'Sirenomelia', 'XPO:0100802', 'abnormal exocrine cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(416667, 'HP:0010497', 'Sirenomelia', 'XPO:0100268', 'abnormal circulatory system', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416668, 'HP:0010497', 'Sirenomelia', 'XPO:0100386', 'abnormal limb', 0.5652173913043478, 5.504475013697824, 1.7638664937410224, 'HP:0040064', 'Abnormality of limbs'),
(416669, 'HP:0010497', 'Sirenomelia', 'XPO:0100218', 'abnormal epithelial cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(416670, 'HP:0010497', 'Sirenomelia', 'XPO:0100533', 'abnormal melanoblast', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(416671, 'HP:0010497', 'Sirenomelia', 'XPO:0101040', 'abnormal axial mesoderm', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416672, 'HP:0010497', 'Sirenomelia', 'XPO:0141772', 'abnormal water homeostasis', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(416673, 'HP:0010497', 'Sirenomelia', 'XPO:0100638', 'abnormal polar body', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(416674, 'HP:0010497', 'Sirenomelia', 'XPO:0107266', 'abnormal dorsal side', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416675, 'HP:0010497', 'Sirenomelia', 'XPO:0100422', 'abnormal notochord', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(416676, 'HP:0010497', 'Sirenomelia', 'XPO:0100081', 'abnormal anatomical entity in vitro', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416677, 'HP:0010497', 'Sirenomelia', 'XPO:0141272', 'absent surface breathing', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(416678, 'HP:0010497', 'Sirenomelia', 'XPO:0100402', 'abnormal zeugopod', 0.52, 5.504475013697824, 1.6918413067196547, 'HP:0040064', 'Abnormality of limbs'),
(416679, 'HP:0010497', 'Sirenomelia', 'XPO:0100531', 'abnormal proliferative region', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416680, 'HP:0010497', 'Sirenomelia', 'XPO:0100976', 'abnormal multiciliated cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(416681, 'HP:0010497', 'Sirenomelia', 'XPO:0141776', 'abnormal metabolic process', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(416682, 'HP:0010497', 'Sirenomelia', 'XPO:0100192', 'abnormal epithelium', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416683, 'HP:0010497', 'Sirenomelia', 'XPO:0107270', 'abnormal proximal-distal axis', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416684, 'HP:0010497', 'Sirenomelia', 'XPO:0100887', 'abnormal right-dorsal blastomere', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(416685, 'HP:0010497', 'Sirenomelia', 'XPO:0115505', 'dead whole organism', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416686, 'HP:0010497', 'Sirenomelia', 'XPO:0101503', 'abnormal organ cortex', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416687, 'HP:0010497', 'Sirenomelia', 'XPO:0100392', 'abnormal cilium', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(416688, 'HP:0010497', 'Sirenomelia', 'XPO:0131725', 'abnormal phosphorylation of RNA polymerase II C-terminal domain', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(416689, 'HP:0010497', 'Sirenomelia', 'XPO:0101569', 'abnormal activin-induced ectoderm', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416690, 'HP:0010497', 'Sirenomelia', 'XPO:0100899', 'abnormal secondary spermatogonium', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(416691, 'HP:0010497', 'Sirenomelia', 'XPO:0141315', 'abnormal anatomical region', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416692, 'HP:0010497', 'Sirenomelia', 'XPO:0100549', 'abnormal mitotic cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(416693, 'HP:0010497', 'Sirenomelia', 'XPO:0107264', 'abnormal anterior side', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416694, 'HP:0010497', 'Sirenomelia', 'XPO:0141786', 'abnormal pigment metabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(416695, 'HP:0010497', 'Sirenomelia', 'XPO:0101157', 'abnormal female organism', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416696, 'HP:0010497', 'Sirenomelia', 'XPO:0100721', 'abnormal centromere', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(416697, 'HP:0010497', 'Sirenomelia', 'XPO:0101326', 'abnormal cementoblast', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(416698, 'HP:0010497', 'Sirenomelia', 'XPO:0100344', 'abnormal portion of organism substance', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416699, 'HP:0010497', 'Sirenomelia', 'XPO:0100186', 'abnormal uveal tract', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416700, 'HP:0010497', 'Sirenomelia', 'XPO:0100282', 'abnormal pelvic girdle primordium', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416701, 'HP:0010497', 'Sirenomelia', 'XPO:0100913', 'abnormal Brachets cleft', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416702, 'HP:0010497', 'Sirenomelia', 'XPO:0100510', 'abnormal forelimb stylopod', 0.4482758620689655, 5.504475013697824, 1.570835217966058, 'HP:0040064', 'Abnormality of limbs'),
(416703, 'HP:0010497', 'Sirenomelia', 'XPO:0100006', 'abnormal anatomical structure', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416704, 'HP:0010497', 'Sirenomelia', 'XPO:0107259', 'abnormal animal-vegetal axis', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416705, 'HP:0010497', 'Sirenomelia', 'XPO:0100573', 'abnormal extraembryonic structure', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416706, 'HP:0010497', 'Sirenomelia', 'XPO:0100002', 'abnormal head', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(416707, 'HP:0010497', 'Sirenomelia', 'XPO:0100842', 'abnormal left-dorsal blastomere', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(416708, 'HP:0010497', 'Sirenomelia', 'XPO:0101141', 'abnormal Keller explant', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416709, 'HP:0010497', 'Sirenomelia', 'XPO:0100415', 'abnormal secretory epithelial cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(416710, 'HP:0010497', 'Sirenomelia', 'XPO:0100823', 'abnormal blood', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(416711, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100587', 'abnormal vestibuloauditory system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(416712, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100417', 'abnormal dense regular connective tissue', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(416713, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100025', 'abnormal oocyte', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(416714, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0141788', 'abnormal hormone biosynthetic process', 0.4074074074074074, 4.758907843651163, 1.392413123563799, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(416715, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100638', 'abnormal polar body', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(416716, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0101467', 'abnormal alkali secreting cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(416717, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0101435', 'abnormal paracrine cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(416718, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100533', 'abnormal melanoblast', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(416719, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100176', 'abnormal stage VI oocyte', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(416720, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0141266', 'abnormal surface breathing', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(416721, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100902', 'abnormal spermatocyte', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(416722, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100026', 'abnormal germ cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(416723, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100239', 'abnormal acellular anatomical structure', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416724, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100862', 'abnormal blastomere V1', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(416725, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100308', 'abnormal early embryonic cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(416726, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100599', 'abnormal adult immune system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(416727, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0141860', 'abnormal malate-aspartate shuttle', 0.4583333333333333, 4.758907843651163, 1.4768771428276568, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(416728, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100721', 'abnormal centromere', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(416729, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100493', 'abnormal liver and biliary system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(416730, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0116434', 'abnormal biological process', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(416731, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100688', 'abnormal adipose tissue', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(416732, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0107271', 'abnormal apical region', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416733, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0107278', 'abnormal medial region', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416734, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100014', 'abnormal tissue', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416735, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0101302', 'abnormal subcortical cytoplasm', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(416736, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100728', 'abnormal cell condensation', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416737, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0107339', 'abnormal yolk platelet', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(416738, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100344', 'abnormal portion of organism substance', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416739, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0125135', 'absent blood', 0.40625, 5.574066539846944, 1.5048137864243607, 'HP:0001871', 'Abnormality of blood and blood-forming tissues'),
(416740, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0101078', 'abnormal mucous gland', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416741, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0141784', 'abnormal cellular hormone metabolic process', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(416742, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100427', 'abnormal olfactory system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(416743, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0141767', 'abnormal temperature homeostasis', 0.4074074074074074, 4.758907843651163, 1.392413123563799, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(416744, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0107253', 'abnormal enteric nervous system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(416745, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0107272', 'abnormal axial region', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416746, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100842', 'abnormal left-dorsal blastomere', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(416747, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0141775', 'abnormal nitrogen compound metabolic process', 0.4782608695652174, 4.758907843651163, 1.508641575552437, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(416748, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100573', 'abnormal extraembryonic structure', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416749, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100402', 'abnormal zeugopod', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(416750, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0141781', 'abnormal secondary metabolic process', 0.4782608695652174, 4.758907843651163, 1.508641575552437, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(416751, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100295', 'abnormal extracellular matrix', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416752, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0131675', 'abnormal spindle microtubule', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(416753, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0141770', 'abnormal urate homeostasis', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(416754, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0131677', 'abnormal actin filament', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(416755, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100969', 'abnormal disaggregated/reaggregated ectoderm treated with activin', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416756, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100384', 'abnormal amputated tissue', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416757, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100062', 'abnormal anatomical space', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416758, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100976', 'abnormal multiciliated cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(416759, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100377', 'abnormal connective tissue', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(416760, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100762', 'abnormal intersomitic region', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416761, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0101480', 'abnormal stage V oocyte', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(416762, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0107284', 'abnormal migrating myoblast', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(416763, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0141789', 'abnormal hormone catabolic process', 0.4074074074074074, 4.758907843651163, 1.392413123563799, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(416764, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0101326', 'abnormal cementoblast', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(416765, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0107267', 'abnormal ventral side', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416766, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:00000000', 'Xenopus phenotype', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(416767, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0141877', 'abnormal 2-deoxyribose 1-phosphate metabolic process', 0.4230769230769231, 4.758907843651163, 1.418937661667548, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(416768, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0101004', 'abnormal acid secreting cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(416769, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0101297', 'abnormal barrier cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(416770, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100225', 'abnormal endocrine system', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(416771, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0101109', 'abnormal egg cell-free extract', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416772, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100807', 'abnormal matrix-based tissue', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416773, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0107262', 'abnormal left-right axis', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416774, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0101378', 'abnormal blastomere D1', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(416775, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0141880', 'abnormal ethanolamine metabolic process', 0.4074074074074074, 4.758907843651163, 1.392413123563799, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(416776, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0101409', 'abnormal perivitelline space', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(416777, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0107269', 'abnormal right side', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416778, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100192', 'abnormal epithelium', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416779, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100006', 'abnormal anatomical structure', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416780, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0141272', 'absent surface breathing', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(416781, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100802', 'abnormal exocrine cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(416782, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0115391', 'abnormally undifferentiated alimentary system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(416783, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100135', 'abnormal surface structure', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416784, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100114', 'abnormal peripheral nervous system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(416785, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100172', 'abnormal stem cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(416786, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0141772', 'abnormal water homeostasis', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(416787, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100610', 'abnormal appendage', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416788, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0141904', 'abnormal glucosamine metabolic process', 0.4782608695652174, 4.758907843651163, 1.508641575552437, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(416789, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0101056', 'abnormal anterior ventral blood island', 0.4642857142857143, 5.574066539846944, 1.6087136056268494, 'HP:0001871', 'Abnormality of blood and blood-forming tissues'),
(416790, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0101569', 'abnormal activin-induced ectoderm', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416791, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100823', 'abnormal blood', 0.5416666666666666, 5.574066539846944, 1.737609289344729, 'UPHENO:0004459', 'abnormal hematopoietic system'),
(416792, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0142056', 'abnormal main body axis', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416793, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0101241', 'abnormal nucleate erythrocyte', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(416794, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0126758', 'abnormally localised blood', 0.41935483870967744, 5.574066539846944, 1.5288923359002506, 'UPHENO:0004459', 'abnormal hematopoietic system'),
(416795, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100251', 'abnormal proteinaceous extracellular matrix', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416796, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0101113', 'abnormal stage IV oocyte', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(416797, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100164', 'abnormal neural nucleus', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(416798, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0101237', 'abnormal mucus secreting cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(416799, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0115509', 'abnormally semi-viable whole organism', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416800, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0101468', 'abnormal stage I oocyte', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(416801, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100742', 'abnormal musculoskeletal system', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416802, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100422', 'abnormal notochord', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(416803, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100549', 'abnormal mitotic cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(416804, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0141841', 'abnormality of whole organism mass', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(416805, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100028', 'abnormal anatomical cluster', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416806, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0101411', 'abnormal marginal zone (sensu neural)', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416807, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0101176', 'abnormal non-ciliated epithelial cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(416808, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0101107', 'abnormal erythroid cell', 0.5, 5.574066539846944, 1.6694410052240456, 'UPHENO:0004459', 'abnormal hematopoietic system'),
(416809, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0141798', 'abnormal lipid metabolic process', 0.44, 4.758907843651163, 1.447038165082909, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(416810, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0101096', 'abnormal tendon', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(416811, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100415', 'abnormal secretory epithelial cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(416812, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100152', 'abnormal alimentary system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(416813, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100202', 'abnormal embryo', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416814, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100887', 'abnormal right-dorsal blastomere', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(416815, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100274', 'abnormal sensory system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(416816, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100186', 'abnormal uveal tract', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416817, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0107266', 'abnormal dorsal side', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416818, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100070', 'abnormal anatomical system', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416819, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0101240', 'abnormal ciliated non-epidermal cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(416820, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100557', 'abnormal prime meridian', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416821, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0107260', 'abnormal anterior-posterior axis', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416822, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100372', 'abnormal hematological system', 0.5909090909090909, 5.574066539846944, 1.8148737123358583, 'HP:0001871', 'Abnormality of blood and blood-forming tissues'),
(416823, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0101157', 'abnormal female organism', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416824, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100745', 'abnormal anterior lymph sac', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(416825, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0101168', 'abnormal circulating cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(416826, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0101484', 'abnormal bone marrow', 0.43333333333333335, 5.574066539846944, 1.5541649957239663, 'UPHENO:0004459', 'abnormal hematopoietic system'),
(416827, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0141267', 'abnormal resting posture', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(416828, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100547', 'abnormal blastomere V2', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(416829, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100899', 'abnormal secondary spermatogonium', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(416830, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100551', 'abnormal oocyte cortex', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(416831, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100704', 'abnormal Merkel cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(416832, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100999', 'abnormal serous membrane', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416833, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0141776', 'abnormal metabolic process', 0.5238095238095238, 4.758907843651163, 1.5788480773767701, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(416834, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0142057', 'abnormal desmosome', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(416835, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0141748', 'abnormal gas homeostasis', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(416836, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0102455', 'abnormal blood morphology', 0.41935483870967744, 5.574066539846944, 1.5288923359002506, 'HP:0001871', 'Abnormality of blood and blood-forming tissues'),
(416837, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100010', 'abnormal multicellular anatomical structure', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416838, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0107312', 'abnormal filopodium', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(416839, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0101347', 'abnormal hindlimb region', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416840, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0131687', 'abnormal astral microtubule', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(416841, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0101220', 'abnormal centriole', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(416842, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0101174', 'abnormal articular system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(416843, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0101023', 'abnormal ultimobranchial body', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(416844, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0101448', 'abnormal myelin accumulating cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(416845, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100265', 'abnormal sensory epithelial cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(416846, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100515', 'abnormal somatic stem cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(416847, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0141271', 'increased surface breathing', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(416848, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100852', 'abnormal interdigital region', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(416849, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0141718', 'abnormal posterior notochord', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(416850, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0141782', 'abnormal methylation', 0.4782608695652174, 4.758907843651163, 1.508641575552437, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(416851, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100574', 'abnormal gastrula cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(416852, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0101451', 'abnormal dorsal lymph space', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(416853, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0101071', 'abnormal endoplasmic reticulum', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(416854, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0102004', 'abnormal hematological system morphology', 0.41935483870967744, 5.574066539846944, 1.5288923359002506, 'HP:0001871', 'Abnormality of blood and blood-forming tissues'),
(416855, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0101463', 'abnormal right-ventral blastomere', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(416856, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0141263', 'abnormal visually guided collision avoidance behavior', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(416857, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0101461', 'abnormal sperm entry point', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(416858, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100023', 'abnormal mesenchyme', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416859, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100104', 'abnormal embryonic structure', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416860, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0101283', 'abnormal left-ventral blastomere', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(416861, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0107263', 'abnormal anatomical side', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416862, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100032', 'abnormal nervous system', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(416863, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0107276', 'abnormal dorsal region', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416864, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100394', 'abnormal marginal zone', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416865, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100363', 'abnormal cardiovascular system', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416866, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0141714', 'abnormal anterior notochord', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(416867, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0107259', 'abnormal animal-vegetal axis', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416868, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100231', 'abnormal compound organ', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416869, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100009', 'abnormal multi-tissue structure', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416870, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0115508', 'abnormally peramorphic growth of whole organism', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416871, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0101503', 'abnormal organ cortex', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416872, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0101405', 'abnormal ring structure', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(416873, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0141276', 'decreased surface breathing', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(416874, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0141794', 'abnormal prosthetic group metabolic process', 0.4782608695652174, 4.758907843651163, 1.508641575552437, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(416875, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0131725', 'abnormal phosphorylation of RNA polymerase II C-terminal domain', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(416876, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100581', 'abnormal immune system', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(416877, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0131667', 'abnormal actin cytoskeleton', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(416878, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0101040', 'abnormal axial mesoderm', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416879, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0107270', 'abnormal proximal-distal axis', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416880, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100640', 'abnormal notochordal sheath', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(416881, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0141795', 'abnormal glycosylation', 0.44, 4.758907843651163, 1.447038165082909, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(416882, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100653', 'abnormal myoblast', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(416883, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0141796', 'abnormal demethylation', 0.4782608695652174, 4.758907843651163, 1.508641575552437, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(416884, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100784', 'abnormal left blastomere', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(416885, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0107288', 'abnormal larval alimentary system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(416886, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100151', 'abnormal primordium', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416887, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100232', 'abnormal lymphatic system', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(416888, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0141778', 'abnormal biosynthetic process', 0.4782608695652174, 4.758907843651163, 1.508641575552437, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(416889, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0101498', 'abnormal stage II oocyte', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(416890, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100458', 'abnormal autopod', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(416891, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100501', 'abnormal urogenital system', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(416892, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0107264', 'abnormal anterior side', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416893, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100258', 'abnormal organ part', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416894, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0115505', 'dead whole organism', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416895, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0142052', 'abnormal nasal region', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(416896, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100277', 'abnormal blastocoel', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416897, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0101188', 'abnormal posterior ventral blood island', 0.4642857142857143, 5.574066539846944, 1.6087136056268494, 'HP:0001871', 'Abnormality of blood and blood-forming tissues'),
(416898, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0101535', 'abnormal absorptive cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(416899, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100069', 'abnormal urinary system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(416900, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0141715', 'abnormal septum', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416901, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0101547', 'abnormal lampbrush chromosome', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(416902, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0107273', 'abnormal basal region', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416903, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100907', 'abnormal cytoplasm', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(416904, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0101575', 'abnormal vitelline membrane', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(416905, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0101061', 'abnormal plasma membrane', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(416906, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0141499', 'abnormal tadpole', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416907, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0142051', 'abnormal cerebrospinal fluid', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(416908, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100218', 'abnormal epithelial cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(416909, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100991', 'abnormal iliac process primordium', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416910, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100120', 'abnormal genital system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(416911, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0141787', 'abnormal hormone metabolic process', 0.4782608695652174, 4.758907843651163, 1.508641575552437, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(416912, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0101132', 'abnormal apoptotic cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(416913, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0131666', 'abnormal adherens junction', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(416914, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0107261', 'abnormal dorsal-ventral axis', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416915, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0116494', 'absent biological process', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(416916, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0131694', 'abnormal RNA polymerase II activity', 0.4230769230769231, 4.758907843651163, 1.418937661667548, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(416917, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100060', 'abnormal regenerating tissue', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416918, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100673', 'abnormal anterior dorsal lateral plate region', 0.41935483870967744, 5.574066539846944, 1.5288923359002506, 'UPHENO:0004459', 'abnormal hematopoietic system'),
(416919, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100585', 'abnormal elastica externa', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(416920, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0115758', 'abnormally decreased mobility of melanoblast', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(416921, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0101110', 'abnormal cell-free extract', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416922, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0131723', 'abnormal pathway-restricted SMAD protein phosphorylation', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(416923, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0107325', 'abnormal adult thrombocyte', 0.41935483870967744, 5.574066539846944, 1.5288923359002506, 'UPHENO:0004459', 'abnormal hematopoietic system'),
(416924, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0141783', 'abnormal collagen metabolic process', 0.4782608695652174, 4.758907843651163, 1.508641575552437, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(416925, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100481', 'abnormal anatomical line', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416926, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100437', 'abnormal proepicardium', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(416927, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0141790', 'abnormal cellular metabolic process', 0.4583333333333333, 4.758907843651163, 1.4768771428276568, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(416928, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0107265', 'abnormal posterior side', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416929, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100643', 'abnormal thoracic region', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416930, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0141777', 'abnormal catabolic process', 0.4782608695652174, 4.758907843651163, 1.508641575552437, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(416931, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0107268', 'abnormal left side', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416932, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0101587', 'abnormal hemangioblast', 0.5, 5.574066539846944, 1.6694410052240456, 'UPHENO:0004459', 'abnormal hematopoietic system'),
(416933, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100674', 'abnormal secondary oogonium', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(416934, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0141738', 'abnormal carbon dioxide homeostasis', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(416935, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0141792', 'abnormal small molecule metabolic process', 0.4782608695652174, 4.758907843651163, 1.508641575552437, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(416936, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0141791', 'abnormal primary metabolic process', 0.4782608695652174, 4.758907843651163, 1.508641575552437, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(416937, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0141264', 'abnormal schooling behavior', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(416938, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100004', 'abnormal cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(416939, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0101311', 'abnormal bottle cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(416940, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0101406', 'abnormal cleavage furrow', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416941, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100915', 'abnormal dermal system', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416942, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0141745', 'abnormal creatinine homeostasis', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(416943, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0131691', 'abnormal molecular function', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(416944, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100002', 'abnormal head', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(416945, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0101333', 'abnormal barrier epithelial cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(416946, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100289', 'abnormal chondroblast', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(416947, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0115512', 'abnormally semi-erect whole organism', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416948, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100786', 'abnormal presumptive axial mesoderm', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416949, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100293', 'abnormal duct', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416950, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0126537', 'abnormally localised hematological system', 0.41935483870967744, 5.574066539846944, 1.5288923359002506, 'HP:0001871', 'Abnormality of blood and blood-forming tissues'),
(416951, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100642', 'abnormal gustatory system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(416952, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100667', 'abnormal vegetal yolk mass', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416953, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100900', 'abnormal angioblast', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(416954, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100307', 'abnormal blastomere', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(416955, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100781', 'abnormal presumptive ectoderm', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416956, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100888', 'abnormal microtubule', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(416957, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0107324', 'abnormal embryonic thrombocyte', 0.41935483870967744, 5.574066539846944, 1.5288923359002506, 'UPHENO:0004459', 'abnormal hematopoietic system'),
(416958, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0101519', 'abnormal hypobranchial placode', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416959, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100268', 'abnormal circulatory system', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416960, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0101072', 'abnormal mitochondrial cloud', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(416961, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100477', 'abnormal pericyte', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(416962, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0101221', 'abnormal larval immune system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(416963, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100754', 'abnormal electrically active cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(416964, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0101264', 'abnormal mitotic spindle', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(416965, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100392', 'abnormal cilium', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(416966, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100273', 'abnormal visual system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(416967, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100917', 'abnormal stage III oocyte', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(416968, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100791', 'abnormal multiciliated cell precursor', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(416969, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100423', 'abnormal process', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416970, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0141892', 'abnormal inositol metabolic process', 0.44, 4.758907843651163, 1.447038165082909, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(416971, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100317', 'abnormal respiratory system', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(416972, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100856', 'abnormal simple organ', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416973, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100531', 'abnormal proliferative region', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416974, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0141786', 'abnormal pigment metabolic process', 0.4782608695652174, 4.758907843651163, 1.508641575552437, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(416975, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0101389', 'abnormal wedge region', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(416976, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0101200', 'abnormal joint region', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416977, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0101497', 'abnormal ciliary axoneme', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(416978, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0101450', 'abnormal myeloid cell', 0.5, 5.574066539846944, 1.6694410052240456, 'HP:0001871', 'Abnormality of blood and blood-forming tissues'),
(416979, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0141911', 'abnormal ribose phosphate metabolic process', 0.4230769230769231, 4.758907843651163, 1.418937661667548, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(416980, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0141898', 'abnormal maltose metabolic process', 0.4230769230769231, 4.758907843651163, 1.418937661667548, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(416981, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0101212', 'abnormal glomeral mesenchyme', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(416982, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0131685', 'abnormal cortical actin cytoskeleton', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(416983, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100108', 'abnormal cell part', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(416984, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0101362', 'abnormal vegetal cortex', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(416985, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0107285', 'abnormal flexural organ', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(416986, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100511', 'abnormal stylopod', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(416987, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100084', 'abnormal anatomical group', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416988, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100989', 'abnormal right blastomere', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(416989, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0101141', 'abnormal Keller explant', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416990, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100429', 'abnormal spermatid', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(416991, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100205', 'abnormal limb segment', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(416992, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0101202', 'abnormal thymus', 0.41935483870967744, 5.574066539846944, 1.5288923359002506, 'UPHENO:0004459', 'abnormal hematopoietic system'),
(416993, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100894', 'abnormal nucleus', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(416994, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100626', 'abnormal primordial germ cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(416995, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0101472', 'abnormal zygote cortex', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(416996, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100912', 'abnormal trabecula', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416997, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100003', 'abnormal organism subdivision', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416998, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100546', 'abnormal whole organism', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(416999, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100503', 'abnormal blastomere D2', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(417000, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0107323', 'abnormal thrombocyte', 0.43333333333333335, 5.574066539846944, 1.5541649957239663, 'HP:0001871', 'Abnormality of blood and blood-forming tissues'),
(417001, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0107258', 'abnormal anatomical axis', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(417002, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0101136', 'abnormal ooplasm', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(417003, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100282', 'abnormal pelvic girdle primordium', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(417004, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100465', 'abnormal skeletal system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(417005, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0141771', 'abnormal urea homeostasis', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(417006, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0101373', 'abnormal oxygen accumulating cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(417007, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0141743', 'abnormal chemical homeostasis within a tissue', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(417008, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0124923', 'absent hematological system', 0.40625, 5.574066539846944, 1.5048137864243607, 'HP:0001871', 'Abnormality of blood and blood-forming tissues'),
(417009, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0101074', 'abnormal germinal vesicle', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(417010, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0101513', 'abnormal basal body', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(417011, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100162', 'abnormal presumptive rhombomere', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(417012, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0141315', 'abnormal anatomical region', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(417013, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0141265', 'abnormal escape behavior', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(417014, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100337', 'abnormal zygote', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(417015, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100031', 'abnormal central nervous system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(417016, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100285', 'abnormal progenitor cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(417017, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100339', 'abnormal circumblastoporal collar', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(417018, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100545', 'abnormal male organism', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(417019, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0141797', 'abnormal hydrogen metabolic process', 0.4782608695652174, 4.758907843651163, 1.508641575552437, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(417020, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100715', 'abnormal ciliated cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(417021, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100691', 'abnormal keratin accumulating cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(417022, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0131669', 'abnormal Roux spot', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(417023, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100956', 'abnormal centrosome', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(417024, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100724', 'abnormal kinetochore', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(417025, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100416', 'abnormal ligament', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(417026, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0101366', 'abnormal morula cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(417027, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100913', 'abnormal Brachets cleft', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(417028, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0101228', 'abnormal mesenchymal stem cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(417029, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100665', 'abnormal egg jelly', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(417030, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0101570', 'abnormal forelimb region', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(417031, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100386', 'abnormal limb', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(417032, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0141907', 'abnormal putrescine metabolic process', 0.44, 4.758907843651163, 1.447038165082909, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(417033, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100616', 'abnormal ventral blood island', 0.48148148148148145, 5.574066539846944, 1.6382337487311942, 'HP:0001871', 'Abnormality of blood and blood-forming tissues'),
(417034, 'HP:0031903', 'Abnormal circulating selenium concentration', 'XPO:0100081', 'abnormal anatomical entity in vitro', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(417035, 'HP:0200063', 'Colorectal polyposis', 'XPO:0101306', 'abnormal ileum', 0.4067796610169492, 8.518562886125473, 1.8614988915306085, 'UPHENO:0076783', 'abnormal intestine morphology'),
(417036, 'HP:0200063', 'Colorectal polyposis', 'XPO:0141240', 'abnormally necrotic rectum', 0.4084507042253521, 12.7526182249875, 2.282283044390683, 'HP:0002034', 'Abnormal rectum morphology'),
(417037, 'HP:0200063', 'Colorectal polyposis', 'XPO:0101321', 'abnormal duodenum', 0.4067796610169492, 8.518562886125473, 1.8614988915306085, 'UPHENO:0076783', 'abnormal intestine morphology'),
(417038, 'HP:0200063', 'Colorectal polyposis', 'XPO:0102473', 'abnormal large intestine morphology', 0.40625, 10.665155383737162, 2.081518526135, 'HP:0002250', 'Abnormal large intestine morphology'),
(417039, 'HP:0200063', 'Colorectal polyposis', 'XPO:0101471', 'abnormal rectum', 0.5087719298245614, 12.7526182249875, 2.54718946775515, 'HP:0002034', 'Abnormal rectum morphology'),
(417040, 'HP:0200063', 'Colorectal polyposis', 'XPO:0101288', 'abnormal external coil of the small intestine', 0.4067796610169492, 8.518562886125473, 1.8614988915306085, 'UPHENO:0076783', 'abnormal intestine morphology'),
(417041, 'HP:0200063', 'Colorectal polyposis', 'XPO:0103103', 'abnormal rectum morphology', 0.4393939393939394, 12.7526182249875, 2.3671550771895373, 'HP:0002034', 'Abnormal rectum morphology'),
(417042, 'HP:0200063', 'Colorectal polyposis', 'XPO:0127034', 'abnormally localised rectum', 0.4393939393939394, 12.7526182249875, 2.3671550771895373, 'HP:0002034', 'Abnormal rectum morphology'),
(417043, 'HP:0200063', 'Colorectal polyposis', 'XPO:0100361', 'abnormal small intestine', 0.41379310344827586, 8.518562886125473, 1.8774777158648677, 'UPHENO:0076783', 'abnormal intestine morphology'),
(417044, 'HP:0200063', 'Colorectal polyposis', 'XPO:0125399', 'absent rectum', 0.4142857142857143, 12.7526182249875, 2.2985272568216293, 'HP:0002034', 'Abnormal rectum morphology'),
(417045, 'HP:0200063', 'Colorectal polyposis', 'XPO:0101537', 'abnormal internal coil of the small intestine', 0.4067796610169492, 8.518562886125473, 1.8614988915306085, 'UPHENO:0076783', 'abnormal intestine morphology'),
(417046, 'HP:0010120', 'Pseudoepiphyses of the hallux', 'XPO:0128670', 'decreased size of the claw primordium', 0.4056603773584906, 7.639349617137506, 1.7603924132026476, 'HP:0001780', 'Abnormal toe morphology'),
(417047, 'HP:0010120', 'Pseudoepiphyses of the hallux', 'XPO:0102948', 'abnormal hindlimb digit 5 morphology', 0.4215686274509804, 7.639349617137506, 1.7945779817870358, 'UPHENO:0088132', 'abnormal pedal digit morphology'),
(417048, 'HP:0010120', 'Pseudoepiphyses of the hallux', 'XPO:0102180', 'abnormal hindlimb digit 3 morphology', 0.4215686274509804, 7.639349617137506, 1.7945779817870358, 'UPHENO:0088132', 'abnormal pedal digit morphology'),
(417049, 'HP:0010120', 'Pseudoepiphyses of the hallux', 'XPO:0139979', 'abnormally necrotic claw primordium', 0.41346153846153844, 7.639349617137506, 1.7772386574535335, 'UPHENO:0088132', 'abnormal pedal digit morphology'),
(417050, 'HP:0010120', 'Pseudoepiphyses of the hallux', 'XPO:0102566', 'abnormal claw primordium morphology', 0.43434343434343436, 7.639349617137506, 1.8215656312243336, 'UPHENO:0088132', 'abnormal pedal digit morphology'),
(417051, 'HP:0010120', 'Pseudoepiphyses of the hallux', 'XPO:0102051', 'abnormal hindlimb digit 2 morphology', 0.4215686274509804, 7.639349617137506, 1.7945779817870358, 'UPHENO:0088132', 'abnormal pedal digit morphology'),
(417052, 'HP:0010120', 'Pseudoepiphyses of the hallux', 'XPO:0101872', 'abnormal hindlimb digit 1 morphology', 0.4215686274509804, 7.639349617137506, 1.7945779817870358, 'HP:0001780', 'Abnormal toe morphology'),
(417053, 'HP:0010120', 'Pseudoepiphyses of the hallux', 'XPO:0101809', 'abnormal hindlimb digit morphology', 0.43, 7.639349617137506, 1.812434918933402, 'HP:0001780', 'Abnormal toe morphology'),
(417054, 'HP:0010120', 'Pseudoepiphyses of the hallux', 'XPO:0141547', 'abnormal hindlimb digit morphology in the regenerating hindlimb', 0.4056603773584906, 7.639349617137506, 1.7603924132026476, 'UPHENO:0088132', 'abnormal pedal digit morphology'),
(417055, 'HP:0010120', 'Pseudoepiphyses of the hallux', 'XPO:0130149', 'increased size of the claw primordium', 0.4056603773584906, 7.639349617137506, 1.7603924132026476, 'HP:0001780', 'Abnormal toe morphology'),
(417056, 'HP:0010120', 'Pseudoepiphyses of the hallux', 'XPO:0102876', 'abnormal hindlimb digit 4 morphology', 0.4215686274509804, 7.639349617137506, 1.7945779817870358, 'HP:0001780', 'Abnormal toe morphology'),
(417057, 'HP:0000287', 'Increased facial adipose tissue', 'XPO:0100627', 'abnormal pharyngeal region', 0.40540540540540543, 3.868794716113063, 1.2523698696136485, 'UPHENO:0002844', 'abnormal head'),
(417058, 'HP:0000287', 'Increased facial adipose tissue', 'XPO:0102320', 'abnormal adipose tissue morphology', 0.4186046511627907, 10.114017760664272, 2.0576138793654017, 'HP:0009124', 'Abnormal adipose tissue morphology'),
(417059, 'HP:0000287', 'Increased facial adipose tissue', 'XPO:0100727', 'abnormal odontogenic papilla', 0.40540540540540543, 3.868794716113063, 1.2523698696136485, 'UPHENO:0002844', 'abnormal head'),
(417060, 'HP:0000287', 'Increased facial adipose tissue', 'XPO:0142052', 'abnormal nasal region', 0.4166666666666667, 3.868794716113063, 1.2696447528267278, 'UPHENO:0002844', 'abnormal head'),
(417061, 'HP:0000287', 'Increased facial adipose tissue', 'XPO:0100002', 'abnormal head', 0.4166666666666667, 3.868794716113063, 1.2696447528267278, 'UPHENO:0002844', 'abnormal head'),
(417062, 'HP:0012508', 'Metamorphopsia', 'XPO:0100881', 'abnormal sclera', 0.40384615384615385, 6.02624522851634, 1.560024345217106, 'HP:0000478', 'Abnormality of the eye'),
(417063, 'HP:0012508', 'Metamorphopsia', 'XPO:0101173', 'abnormal retinal layer', 0.4375, 6.02624522851634, 1.6237248188889333, 'HP:0000478', 'Abnormality of the eye'),
(417064, 'HP:0012508', 'Metamorphopsia', 'XPO:0100485', 'abnormal retina', 0.40384615384615385, 6.02624522851634, 1.560024345217106, 'HP:0000478', 'Abnormality of the eye'),
(417065, 'HP:0012508', 'Metamorphopsia', 'XPO:0100918', 'abnormal lens', 0.40384615384615385, 6.02624522851634, 1.560024345217106, 'HP:0000478', 'Abnormality of the eye'),
(417066, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0102176', 'abnormal neuromast support cell morphology', 0.4772727272727273, 7.420886955069779, 1.881963590463099, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(417067, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0103104', 'abnormal zygote cortex morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(417068, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0102434', 'abnormal exocrine cell morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(417069, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0102520', 'abnormal microtubule morphology', 0.4166666666666667, 2.786899518863159, 1.0775936770692605, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(417070, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0100507', 'abnormal skin', 0.42857142857142855, 6.8660902472206855, 1.7154037734456928, 'HP:0000951', 'Abnormality of the skin'),
(417071, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0101804', 'abnormal stem cell morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(417072, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0100994', 'abnormal granular gland', 0.40540540540540543, 6.8660902472206855, 1.6683974647021622, 'HP:0000951', 'Abnormality of the skin'),
(417073, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0102727', 'abnormal skin seromucous gland morphology', 0.4883720930232558, 7.420886955069779, 1.9037211177944116, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(417074, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0102539', 'abnormal cytoplasm morphology', 0.4166666666666667, 2.786899518863159, 1.0775936770692605, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(417075, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0102764', 'abnormal apoptotic cell morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(417076, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0141219', 'abnormally necrotic granular gland', 0.42, 7.420886955069779, 1.7654383368244009, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(417077, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0130281', 'increased size of the dermis', 0.42857142857142855, 7.420886955069779, 1.7833620281931915, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(417078, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0141299', 'abnormal actin filament morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(417079, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0101640', 'abnormal epidermis morphology', 0.43636363636363634, 11.189682030596343, 2.209699151609526, 'HP:0011124', 'Abnormal epidermal morphology'),
(417080, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0101890', 'abnormal organ part morphology', 0.43333333333333335, 2.786899518863159, 1.0989342374200721, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(417081, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0102165', 'abnormal melanoblast morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(417082, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0101642', 'abnormal multicellular anatomical structure morphology', 0.41935483870967744, 2.786899518863159, 1.0810641970914296, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(417083, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0140581', 'abnormally necrotic stratum compactum', 0.42857142857142855, 7.420886955069779, 1.7833620281931915, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(417084, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0102381', 'abnormal mucociliary epithelium morphology', 0.41509433962264153, 8.516821552129047, 1.8802352028043958, 'UPHENO:0087435', 'abnormal skin epidermis morphology'),
(417085, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0103202', 'abnormal forelimb region morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(417086, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0141336', 'increased pigmentation in the epidermis', 0.41379310344827586, 11.189682030596343, 2.151793032342996, 'UPHENO:0020750', 'abnormal skin epidermis morphology'),
(417087, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0141057', 'abnormally necrotic iridophore', 0.4117647058823529, 7.420886955069779, 1.7480444314835069, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(417088, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0128502', 'decreased size of the anatomical line', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(417089, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0102636', 'abnormal acid secreting cell morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(417090, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0103005', 'abnormal oxygen accumulating cell morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(417091, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0103167', 'abnormal absorptive cell morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(417092, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0107399', 'abnormal filopodium morphology', 0.4166666666666667, 2.786899518863159, 1.0775936770692605, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(417093, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0141296', 'abnormal adherens junction morphology', 0.4166666666666667, 2.786899518863159, 1.0775936770692605, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(417094, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0102615', 'abnormal skin gland morphology', 0.5121951219512195, 7.420886955069779, 1.9496004972655756, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(417095, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0107345', 'abnormal anatomical axis morphology', 0.43333333333333335, 2.786899518863159, 1.0989342374200721, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(417096, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0103093', 'abnormal sperm entry point morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(417097, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0140061', 'abnormally necrotic pigment cell', 0.4375, 7.420886955069779, 1.8018429573198183, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(417098, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0102979', 'abnormal hindlimb region morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(417099, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0102588', 'abnormal centrosome morphology', 0.4166666666666667, 2.786899518863159, 1.0775936770692605, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(417100, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0129422', 'decreased size of the skin seromucous gland', 0.40384615384615385, 7.420886955069779, 1.7311547172139254, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(417101, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0101638', 'abnormal anatomical structure morphology', 0.4642857142857143, 2.786899518863159, 1.1375050038386183, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(417102, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0102285', 'abnormal myoblast morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(417103, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0103145', 'abnormal basal body morphology', 0.4166666666666667, 2.786899518863159, 1.0775936770692605, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(417104, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0107346', 'abnormal animal-vegetal axis morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(417105, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0102113', 'abnormal anatomical line morphology', 0.4642857142857143, 2.786899518863159, 1.1375050038386183, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(417106, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0102703', 'abnormal endoplasmic reticulum morphology', 0.4166666666666667, 2.786899518863159, 1.0775936770692605, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(417107, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0102055', 'abnormal process morphology', 0.41935483870967744, 2.786899518863159, 1.0810641970914296, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(417108, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0102945', 'abnormal Eberth-Kastschenko layer morphology', 0.4772727272727273, 7.420886955069779, 1.881963590463099, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(417109, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0102873', 'abnormal nucleate erythrocyte morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(417110, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0102929', 'abnormal barrier cell morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(417111, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0130126', 'increased size of the stratum compactum', 0.4117647058823529, 7.420886955069779, 1.7480444314835069, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(417112, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0102356', 'abnormal kinetochore morphology', 0.4166666666666667, 2.786899518863159, 1.0775936770692605, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(417113, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0103019', 'abnormal melanophore morphology', 0.45652173913043476, 7.420886955069779, 1.8405967017841829, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(417114, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0103223', 'abnormal xanthophore morphology', 0.45652173913043476, 7.420886955069779, 1.8405967017841829, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(417115, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0130438', 'increased size of the granular gland', 0.40384615384615385, 7.420886955069779, 1.7311547172139254, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(417116, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0102840', 'abnormal stratum spongiosum morphology', 0.4772727272727273, 7.420886955069779, 1.881963590463099, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(417117, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0141330', 'edematous epidermis', 0.42105263157894735, 11.189682030596343, 2.1705863414096775, 'HP:0011124', 'Abnormal epidermal morphology'),
(417118, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0101658', 'abnormal germ cell morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(417119, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0142064', 'abnormal desmosome morphology', 0.4166666666666667, 2.786899518863159, 1.0775936770692605, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(417120, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0102852', 'abnormal centriole morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(417121, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0102064', 'abnormal epidermis inner layer morphology', 0.4074074074074074, 8.516821552129047, 1.8627442626148192, 'UPHENO:0087435', 'abnormal skin epidermis morphology'),
(417122, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0128102', 'decreased size of the portion of organism substance', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(417123, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0102526', 'abnormal nucleus morphology', 0.4166666666666667, 2.786899518863159, 1.0775936770692605, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(417124, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0102275', 'abnormal thoracic region morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(417125, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0102886', 'abnormal stratum compactum morphology', 0.4772727272727273, 7.420886955069779, 1.881963590463099, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(417126, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0101636', 'abnormal cell morphology', 0.42857142857142855, 2.786899518863159, 1.092879457252359, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(417127, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0115317', 'abnormally incomplete structure of epidermis', 0.42857142857142855, 11.189682030596343, 2.189880821668777, 'UPHENO:0020750', 'abnormal skin epidermis morphology'),
(417128, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0102561', 'abnormal dermis morphology', 0.5, 7.420886955069779, 1.9262511460178005, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(417129, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0130356', 'increased size of the skin gland', 0.42857142857142855, 7.420886955069779, 1.7833620281931915, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(417130, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0139841', 'abnormally necrotic anatomical region', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(417131, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0100983', 'abnormal skin gland', 0.4166666666666667, 6.8660902472206855, 1.6914109306558096, 'HP:0000951', 'Abnormality of the skin'),
(417132, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0102869', 'abnormal mucus secreting cell morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(417133, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0107359', 'abnormal axial region morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(417134, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0102336', 'abnormal Merkel cell morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(417135, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0101713', 'abnormal anatomical entity in vitro morphology', 0.4642857142857143, 2.786899518863159, 1.1375050038386183, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(417136, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0102323', 'abnormal keratin accumulating cell morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(417137, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0128175', 'decreased size of the skin', 0.42857142857142855, 7.420886955069779, 1.7833620281931915, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(417138, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0101969', 'abnormal zygote morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(417139, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0141505', 'abnormal tadpole morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(417140, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0141316', 'abnormal anatomical region morphology', 0.43333333333333335, 2.786899518863159, 1.0989342374200721, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(417141, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0102139', 'abnormal skin morphology', 0.5121951219512195, 7.420886955069779, 1.9496004972655756, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(417142, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0103147', 'abnormal neuromast mantle cell morphology', 0.4772727272727273, 7.420886955069779, 1.881963590463099, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(417143, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0140269', 'abnormally necrotic anatomical line', 0.43333333333333335, 2.786899518863159, 1.0989342374200721, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(417144, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0103179', 'abnormal lampbrush chromosome morphology', 0.4166666666666667, 2.786899518863159, 1.0775936770692605, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(417145, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0100929', 'abnormal dermis', 0.40540540540540543, 6.8660902472206855, 1.6683974647021622, 'HP:0000951', 'Abnormality of the skin'),
(417146, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0140481', 'abnormally necrotic melanophore', 0.4117647058823529, 7.420886955069779, 1.7480444314835069, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(417147, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0141285', 'abnormal cortical actin cytoskeleton morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(417148, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0115316', 'abnormally neoplastic epidermis', 0.41379310344827586, 11.189682030596343, 2.151793032342996, 'UPHENO:0020750', 'abnormal skin epidermis morphology'),
(417149, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0102693', 'abnormal plasma membrane morphology', 0.4166666666666667, 2.786899518863159, 1.0775936770692605, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(417150, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0139718', 'abnormally necrotic anatomical structure', 0.43333333333333335, 2.786899518863159, 1.0989342374200721, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(417151, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0130706', 'increased size of the stratum spongiosum', 0.4117647058823529, 7.420886955069779, 1.7480444314835069, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(417152, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0103201', 'abnormal activin-induced ectoderm morphology', 0.43333333333333335, 2.786899518863159, 1.0989342374200721, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(417153, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0115510', 'abnormal degeneration of whole organism', 0.41935483870967744, 2.786899518863159, 1.0810641970914296, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(417154, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0102896', 'abnormal mitotic spindle morphology', 0.4166666666666667, 2.786899518863159, 1.0775936770692605, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(417155, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0103080', 'abnormal myelin accumulating cell morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(417156, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0101095', 'abnormal skin seromucous gland', 0.40540540540540543, 6.8660902472206855, 1.6683974647021622, 'HP:0000951', 'Abnormality of the skin'),
(417157, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0102626', 'abnormal granular gland morphology', 0.4883720930232558, 7.420886955069779, 1.9037211177944116, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(417158, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0102773', 'abnormal Keller explant morphology', 0.43333333333333335, 2.786899518863159, 1.0989342374200721, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(417159, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0102347', 'abnormal ciliated cell morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(417160, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0129993', 'increased size of the Eberth-Kastschenko layer', 0.4117647058823529, 7.420886955069779, 1.7480444314835069, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(417161, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0102832', 'abnormal joint region morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(417162, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0107349', 'abnormal left-right axis morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(417163, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0140144', 'abnormally necrotic portion of organism substance', 0.43333333333333335, 2.786899518863159, 1.0989342374200721, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(417164, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0102646', 'abnormal goblet cell morphology', 0.4375, 7.420886955069779, 1.8018429573198183, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(417165, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0102133', 'abnormal urogenital system morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(417166, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0102965', 'abnormal barrier epithelial cell morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(417167, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0128878', 'decreased size of the skin gland', 0.42857142857142855, 7.420886955069779, 1.7833620281931915, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(417168, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0102353', 'abnormal centromere morphology', 0.4166666666666667, 2.786899518863159, 1.0775936770692605, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(417169, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0102386', 'abnormal electrically active cell morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(417170, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0102958', 'abnormal cementoblast morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(417171, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0128513', 'decreased size of the Eberth-Kastschenko layer', 0.4117647058823529, 7.420886955069779, 1.7480444314835069, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(417172, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0101871', 'abnormal acellular anatomical structure morphology', 0.41935483870967744, 2.786899518863159, 1.0810641970914296, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(417173, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0140539', 'abnormally necrotic Eberth-Kastschenko layer', 0.42857142857142855, 7.420886955069779, 1.7833620281931915, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(417174, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0102789', 'abnormal female organism morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(417175, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0107357', 'abnormal proximal-distal axis morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(417176, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0102205', 'abnormal extraembryonic structure morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(417177, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0107348', 'abnormal dorsal-ventral axis morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(417178, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0129487', 'increased size of the anatomical structure', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(417179, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0102181', 'abnormal mitotic cell morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(417180, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0102910', 'abnormal pigment cell morphology', 0.4772727272727273, 7.420886955069779, 1.881963590463099, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(417181, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0103099', 'abnormal alkali secreting cell morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(417182, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0128803', 'decreased size of the dermis', 0.42857142857142855, 7.420886955069779, 1.7833620281931915, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(417183, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0102178', 'abnormal whole organism morphology', 0.43333333333333335, 2.786899518863159, 1.0989342374200721, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(417184, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0141205', 'abnormally necrotic skin seromucous gland', 0.42, 7.420886955069779, 1.7654383368244009, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(417185, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0102954', 'abnormal iridophore morphology', 0.45652173913043476, 7.420886955069779, 1.8405967017841829, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(417186, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0102024', 'abnormal cilium morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(417187, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0101694', 'abnormal anatomical space morphology', 0.43333333333333335, 2.786899518863159, 1.0989342374200721, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(417188, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0102601', 'abnormal disaggregated/reaggregated ectoderm treated with activin morphology', 0.43333333333333335, 2.786899518863159, 1.0989342374200721, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(417189, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0128007', 'decreased size of the anatomical structure', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(417190, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0103161', 'abnormal skin mucous gland morphology', 0.44680851063829785, 7.420886955069779, 1.8209106095604752, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(417191, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0107350', 'abnormal anatomical side morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(417192, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0103043', 'abnormal marginal zone (sensu neural) morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(417193, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0129230', 'decreased size of the stratum spongiosum', 0.4117647058823529, 7.420886955069779, 1.7480444314835069, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(417194, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0102742', 'abnormal cell-free extract morphology', 0.43333333333333335, 2.786899518863159, 1.0989342374200721, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(417195, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0102741', 'abnormal egg cell-free extract morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(417196, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0141342', 'decreased pigmentation in the epidermis', 0.41379310344827586, 11.189682030596343, 2.151793032342996, 'HP:0011124', 'Abnormal epidermal morphology'),
(417197, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0140701', 'abnormally necrotic neuromast support cell', 0.4375, 7.420886955069779, 1.8018429573198183, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(417198, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0102177', 'abnormal male organism morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(417199, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0101917', 'abnormal progenitor cell morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(417200, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0140154', 'abnormally necrotic skin', 0.44680851063829785, 7.420886955069779, 1.8209106095604752, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(417201, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0102423', 'abnormal multiciliated cell precursor morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(417202, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0101976', 'abnormal portion of organism substance morphology', 0.4642857142857143, 2.786899518863159, 1.1375050038386183, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(417203, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0140540', 'abnormally necrotic dermis', 0.44680851063829785, 7.420886955069779, 1.8209106095604752, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(417204, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0101716', 'abnormal anatomical group morphology', 0.41935483870967744, 2.786899518863159, 1.0810641970914296, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(417205, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0102109', 'abnormal pericyte morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(417206, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0140156', 'abnormally necrotic neuromast mantle cell', 0.4375, 7.420886955069779, 1.8018429573198183, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(417207, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0140591', 'abnormally necrotic skin gland', 0.44680851063829785, 7.420886955069779, 1.8209106095604752, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(417208, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0129582', 'increased size of the portion of organism substance', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(417209, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0101740', 'abnormal cell part morphology', 0.4411764705882353, 2.786899518863159, 1.1088347458553505, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(417210, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0101921', 'abnormal chondroblast morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(417211, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0130896', 'increased size of the skin seromucous gland', 0.40384615384615385, 7.420886955069779, 1.7311547172139254, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(417212, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0107347', 'abnormal anterior-posterior axis morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(417213, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0129982', 'increased size of the anatomical line', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(417214, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0128960', 'decreased size of the granular gland', 0.40384615384615385, 7.420886955069779, 1.7311547172139254, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(417215, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0128647', 'decreased size of the stratum compactum', 0.4117647058823529, 7.420886955069779, 1.7480444314835069, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(417216, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0102360', 'abnormal cell condensation morphology', 0.41935483870967744, 2.786899518863159, 1.0810641970914296, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(417217, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0140235', 'abnormally necrotic stratum spongiosum', 0.42857142857142855, 7.420886955069779, 1.7833620281931915, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(417218, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0103067', 'abnormal paracrine cell morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(417219, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0129655', 'increased size of the skin', 0.42857142857142855, 7.420886955069779, 1.7833620281931915, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(417220, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0140698', 'abnormally necrotic xanthophore', 0.4117647058823529, 7.420886955069779, 1.7480444314835069, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(417221, 'HP:0025092', 'Epidermal acanthosis', 'XPO:0141277', 'abnormal actin cytoskeleton morphology', 0.4166666666666667, 2.786899518863159, 1.0775936770692605, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(417222, 'HP:0007690', 'Map-dot-fingerprint corneal dystrophy', 'XPO:0141337', 'increased pigmentation in the eye', 0.41333333333333333, 6.887869297006056, 1.6873013886368484, 'HP:0012372', 'Abnormal eye morphology'),
(417223, 'HP:0007690', 'Map-dot-fingerprint corneal dystrophy', 'XPO:0100779', 'abnormal optic choroid vascular plexus', 0.47692307692307695, 6.887869297006056, 1.8124524320853552, 'HP:0012372', 'Abnormal eye morphology'),
(417224, 'HP:0007690', 'Map-dot-fingerprint corneal dystrophy', 'XPO:0127645', 'abnormally localised hyaloid vein', 0.4025974025974026, 6.887869297006056, 1.6652442128423794, 'HP:0012372', 'Abnormal eye morphology'),
(417225, 'HP:0007690', 'Map-dot-fingerprint corneal dystrophy', 'XPO:0103022', 'abnormal ciliary body morphology', 0.4050632911392405, 8.412768222102876, 1.8459966369515974, 'UPHENO:0087597', 'abnormal anterior segment of eyeball morphology'),
(417226, 'HP:0007690', 'Map-dot-fingerprint corneal dystrophy', 'XPO:0141343', 'decreased pigmentation in the eye', 0.41333333333333333, 6.887869297006056, 1.6873013886368484, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(417227, 'HP:0007690', 'Map-dot-fingerprint corneal dystrophy', 'XPO:0125589', 'absent hyaloid blood vessel', 0.40789473684210525, 6.887869297006056, 1.6761639640277146, 'HP:0012372', 'Abnormal eye morphology'),
(417228, 'HP:0007690', 'Map-dot-fingerprint corneal dystrophy', 'XPO:0100710', 'abnormal hyaloid vein', 0.4696969696969697, 6.887869297006056, 1.7986693238259617, 'HP:0012372', 'Abnormal eye morphology'),
(417229, 'HP:0007690', 'Map-dot-fingerprint corneal dystrophy', 'XPO:0103210', 'abnormal pupil morphology', 0.43037974683544306, 9.014833150514745, 1.969721200851099, 'UPHENO:0021038', 'abnormal anterior segment of eyeball morphology'),
(417230, 'HP:0007690', 'Map-dot-fingerprint corneal dystrophy', 'XPO:0129260', 'decreased size of the cornea', 0.4470588235294118, 10.582693223545188, 2.1751060623084086, 'UPHENO:0020998', 'abnormal cornea morphology'),
(417231, 'HP:0007690', 'Map-dot-fingerprint corneal dystrophy', 'XPO:0101823', 'abnormal lens epithelium morphology', 0.4146341463414634, 9.014833150514745, 1.9333539892565992, 'UPHENO:0021038', 'abnormal anterior segment of eyeball morphology'),
(417232, 'HP:0007690', 'Map-dot-fingerprint corneal dystrophy', 'XPO:0102805', 'abnormal retinal layer morphology', 0.4025974025974026, 6.887869297006056, 1.6652442128423794, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(417233, 'HP:0007690', 'Map-dot-fingerprint corneal dystrophy', 'XPO:0102862', 'abnormal iris morphology', 0.43037974683544306, 9.014833150514745, 1.969721200851099, 'UPHENO:0021038', 'abnormal anterior segment of eyeball morphology'),
(417234, 'HP:0007690', 'Map-dot-fingerprint corneal dystrophy', 'XPO:0102476', 'abnormal lens transitional zone morphology', 0.4533333333333333, 9.014833150514745, 2.021564829919309, 'UPHENO:0021038', 'abnormal anterior segment of eyeball morphology'),
(417235, 'HP:0007690', 'Map-dot-fingerprint corneal dystrophy', 'XPO:0100371', 'abnormal hyaloid blood vessel', 0.484375, 6.887869297006056, 1.8265573330003382, 'HP:0012372', 'Abnormal eye morphology'),
(417236, 'HP:0007690', 'Map-dot-fingerprint corneal dystrophy', 'XPO:0140250', 'abnormally necrotic iris', 0.40476190476190477, 9.014833150514745, 1.910199213986099, 'UPHENO:0021038', 'abnormal anterior segment of eyeball morphology'),
(417237, 'HP:0007690', 'Map-dot-fingerprint corneal dystrophy', 'XPO:0141141', 'abnormally necrotic cornea', 0.4810126582278481, 10.582693223545188, 2.256193564095799, 'UPHENO:0020998', 'abnormal cornea morphology'),
(417238, 'HP:0007690', 'Map-dot-fingerprint corneal dystrophy', 'XPO:0133354', 'fused eyes', 0.41333333333333333, 6.887869297006056, 1.6873013886368484, 'HP:0012372', 'Abnormal eye morphology'),
(417239, 'HP:0007690', 'Map-dot-fingerprint corneal dystrophy', 'XPO:0140375', 'abnormally necrotic lens', 0.4358974358974359, 9.014833150514745, 1.982307406875276, 'UPHENO:0021038', 'abnormal anterior segment of eyeball morphology'),
(417240, 'HP:0007690', 'Map-dot-fingerprint corneal dystrophy', 'XPO:0128807', 'decreased size of the lens transitional zone', 0.4146341463414634, 9.014833150514745, 1.9333539892565992, 'UPHENO:0021038', 'abnormal anterior segment of eyeball morphology'),
(417241, 'HP:0007690', 'Map-dot-fingerprint corneal dystrophy', 'XPO:0127230', 'abnormally localised hyaloid blood vessel', 0.4246575342465753, 6.887869297006056, 1.7102589253909142, 'HP:0012372', 'Abnormal eye morphology'),
(417242, 'HP:0007690', 'Map-dot-fingerprint corneal dystrophy', 'XPO:0133369', 'eye fused with brain', 0.41333333333333333, 6.887869297006056, 1.6873013886368484, 'HP:0012372', 'Abnormal eye morphology'),
(417243, 'HP:0007690', 'Map-dot-fingerprint corneal dystrophy', 'XPO:0103048', 'abnormal cornea morphology', 0.5205479452054794, 10.582693223545188, 2.347083128535587, 'UPHENO:0020998', 'abnormal cornea morphology'),
(417244, 'HP:0007690', 'Map-dot-fingerprint corneal dystrophy', 'XPO:0141638', 'neoplastic eye', 0.41333333333333333, 6.887869297006056, 1.6873013886368484, 'HP:0012372', 'Abnormal eye morphology'),
(417245, 'HP:0007690', 'Map-dot-fingerprint corneal dystrophy', 'XPO:0133372', 'eye fused with olfactory epithelium', 0.41333333333333333, 6.887869297006056, 1.6873013886368484, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(417246, 'HP:0007690', 'Map-dot-fingerprint corneal dystrophy', 'XPO:0140473', 'abnormally necrotic lens transitional zone', 0.425, 9.014833150514745, 1.957371729889028, 'UPHENO:0021038', 'abnormal anterior segment of eyeball morphology'),
(417247, 'HP:0007690', 'Map-dot-fingerprint corneal dystrophy', 'XPO:0102550', 'abnormal lens morphology', 0.4657534246575342, 9.014833150514745, 2.0490703776514145, 'UPHENO:0021038', 'abnormal anterior segment of eyeball morphology'),
(417248, 'HP:0007690', 'Map-dot-fingerprint corneal dystrophy', 'XPO:0101817', 'abnormal eye morphology', 0.4305555555555556, 6.887869297006056, 1.7220947685207388, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(417249, 'HP:0007690', 'Map-dot-fingerprint corneal dystrophy', 'XPO:0115423', 'abnormally incomplete structure of eye', 0.4246575342465753, 6.887869297006056, 1.7102589253909142, 'HP:0012372', 'Abnormal eye morphology'),
(417250, 'HP:0007690', 'Map-dot-fingerprint corneal dystrophy', 'XPO:0127907', 'abnormally localised optic choroid vascular plexus', 0.40789473684210525, 6.887869297006056, 1.6761639640277146, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(417251, 'HP:0007690', 'Map-dot-fingerprint corneal dystrophy', 'XPO:0101315', 'abnormal hyaloid vascular plexus', 0.4696969696969697, 6.887869297006056, 1.7986693238259617, 'HP:0012372', 'Abnormal eye morphology'),
(417252, 'HP:0007690', 'Map-dot-fingerprint corneal dystrophy', 'XPO:0102003', 'abnormal hyaloid blood vessel morphology', 0.4025974025974026, 6.887869297006056, 1.6652442128423794, 'HP:0012372', 'Abnormal eye morphology'),
(417253, 'HP:0007690', 'Map-dot-fingerprint corneal dystrophy', 'XPO:0129947', 'increased size of the lens', 0.41975308641975306, 9.014833150514745, 1.9452516645636548, 'UPHENO:0021038', 'abnormal anterior segment of eyeball morphology'),
(417254, 'HP:0007690', 'Map-dot-fingerprint corneal dystrophy', 'XPO:0130893', 'increased size of the pupil', 0.40476190476190477, 9.014833150514745, 1.910199213986099, 'UPHENO:0021038', 'abnormal anterior segment of eyeball morphology'),
(417255, 'HP:0007690', 'Map-dot-fingerprint corneal dystrophy', 'XPO:0102513', 'abnormal sclera morphology', 0.4246575342465753, 6.887869297006056, 1.7102589253909142, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(417256, 'HP:0007690', 'Map-dot-fingerprint corneal dystrophy', 'XPO:0130285', 'increased size of the lens transitional zone', 0.4146341463414634, 9.014833150514745, 1.9333539892565992, 'UPHENO:0021038', 'abnormal anterior segment of eyeball morphology'),
(417257, 'HP:0007690', 'Map-dot-fingerprint corneal dystrophy', 'XPO:0141323', 'edematous eye', 0.4189189189189189, 6.887869297006056, 1.6986638159319787, 'HP:0012372', 'Abnormal eye morphology'),
(417258, 'HP:0007690', 'Map-dot-fingerprint corneal dystrophy', 'XPO:0130736', 'increased size of the cornea', 0.4470588235294118, 10.582693223545188, 2.1751060623084086, 'UPHENO:0020998', 'abnormal cornea morphology'),
(417259, 'HP:0007690', 'Map-dot-fingerprint corneal dystrophy', 'XPO:0128467', 'decreased size of the lens', 0.41975308641975306, 9.014833150514745, 1.9452516645636548, 'UPHENO:0021038', 'abnormal anterior segment of eyeball morphology'),
(417260, 'HP:0007690', 'Map-dot-fingerprint corneal dystrophy', 'XPO:0133371', 'eye fused with olfactory pit', 0.41333333333333333, 6.887869297006056, 1.6873013886368484, 'HP:0012372', 'Abnormal eye morphology'),
(417261, 'HP:0005787', 'Lumbar platyspondyly', 'XPO:0100584', 'abnormal vertebral column', 0.4032258064516129, 8.05344015541032, 1.8020418700394085, 'UPHENO:0002813', 'abnormal vertebral column'),
(417262, 'HP:0500066', 'Latent myopia', 'XPO:0100727', 'abnormal odontogenic papilla', 0.40540540540540543, 3.868794716113063, 1.2523698696136485, 'UPHENO:0002844', 'abnormal head'),
(417263, 'HP:0500066', 'Latent myopia', 'XPO:0100627', 'abnormal pharyngeal region', 0.40540540540540543, 3.868794716113063, 1.2523698696136485, 'UPHENO:0002844', 'abnormal head'),
(417264, 'HP:0500066', 'Latent myopia', 'XPO:0100485', 'abnormal retina', 0.42857142857142855, 6.02624522851634, 1.6070707907578319, 'HP:0000478', 'Abnormality of the eye'),
(417265, 'HP:0500066', 'Latent myopia', 'XPO:0100918', 'abnormal lens', 0.42857142857142855, 6.02624522851634, 1.6070707907578319, 'HP:0000478', 'Abnormality of the eye'),
(417266, 'HP:0500066', 'Latent myopia', 'XPO:0101554', 'abnormal peripheral retina', 0.42, 6.02624522851634, 1.590918915588366, 'HP:0000478', 'Abnormality of the eye'),
(417267, 'HP:0500066', 'Latent myopia', 'XPO:0101578', 'abnormal pupil', 0.42, 6.02624522851634, 1.590918915588366, 'HP:0000478', 'Abnormality of the eye'),
(417268, 'HP:0500066', 'Latent myopia', 'XPO:0101173', 'abnormal retinal layer', 0.4666666666666667, 6.02624522851634, 1.6769757819681315, 'HP:0000478', 'Abnormality of the eye'),
(417269, 'HP:0500066', 'Latent myopia', 'XPO:0101230', 'abnormal iris', 0.4117647058823529, 6.02624522851634, 1.5752444553449358, 'HP:0000478', 'Abnormality of the eye'),
(417270, 'HP:0500066', 'Latent myopia', 'XPO:0101289', 'abnormal orbital region', 0.41304347826086957, 5.757493499662858, 1.5421073701805246, 'HP:0000315', 'Abnormality of the orbital region'),
(417271, 'HP:0500066', 'Latent myopia', 'XPO:0101390', 'abnormal ciliary body', 0.4117647058823529, 6.02624522851634, 1.5752444553449358, 'HP:0000478', 'Abnormality of the eye'),
(417272, 'HP:0500066', 'Latent myopia', 'XPO:0100881', 'abnormal sclera', 0.42857142857142855, 6.02624522851634, 1.6070707907578319, 'HP:0000478', 'Abnormality of the eye'),
(417273, 'HP:0500066', 'Latent myopia', 'XPO:0142052', 'abnormal nasal region', 0.4166666666666667, 3.868794716113063, 1.2696447528267278, 'UPHENO:0002844', 'abnormal head'),
(417274, 'HP:0500066', 'Latent myopia', 'XPO:0100844', 'abnormal lens transitional zone', 0.4117647058823529, 6.02624522851634, 1.5752444553449358, 'HP:0000478', 'Abnormality of the eye'),
(417275, 'HP:0500066', 'Latent myopia', 'XPO:0127803', 'abnormally localised retinal layer', 0.4074074074074074, 6.02624522851634, 1.5668876618797856, 'HP:0000478', 'Abnormality of the eye'),
(417276, 'HP:0500066', 'Latent myopia', 'XPO:0100002', 'abnormal head', 0.4166666666666667, 3.868794716113063, 1.2696447528267278, 'UPHENO:0002844', 'abnormal head'),
(417277, 'HP:0500066', 'Latent myopia', 'XPO:0101416', 'abnormal cornea', 0.42, 6.02624522851634, 1.590918915588366, 'HP:0000478', 'Abnormality of the eye'),
(417278, 'HP:0500066', 'Latent myopia', 'XPO:0100564', 'abnormal central retina', 0.42, 6.02624522851634, 1.590918915588366, 'HP:0000478', 'Abnormality of the eye'),
(417279, 'HP:0033302', 'Elevated circulating 4-hydroxyphenylacetic acid concentration', 'XPO:0141888', 'abnormal threonine metabolic process', 0.6363636363636364, 9.119292702704945, 2.4089803372708736, 'HP:0004354', 'Abnormal circulating carboxylic acid concentration'),
(417280, 'HP:0033302', 'Elevated circulating 4-hydroxyphenylacetic acid concentration', 'XPO:0141889', 'abnormal homoserine metabolic process', 0.625, 9.119292702704945, 2.387374696018744, 'HP:0004354', 'Abnormal circulating carboxylic acid concentration'),
(417281, 'HP:0033302', 'Elevated circulating 4-hydroxyphenylacetic acid concentration', 'XPO:0141848', 'abnormal proline metabolic process', 0.6363636363636364, 9.119292702704945, 2.4089803372708736, 'HP:0004354', 'Abnormal circulating carboxylic acid concentration'),
(417282, 'HP:0033302', 'Elevated circulating 4-hydroxyphenylacetic acid concentration', 'XPO:0141896', 'abnormal lysine metabolic process', 0.6363636363636364, 9.119292702704945, 2.4089803372708736, 'HP:0004354', 'Abnormal circulating carboxylic acid concentration'),
(417283, 'HP:0033302', 'Elevated circulating 4-hydroxyphenylacetic acid concentration', 'XPO:0141905', 'abnormal ornithine metabolic process', 0.6481481481481481, 9.119292702704945, 2.4311833903840183, 'HP:0004354', 'Abnormal circulating carboxylic acid concentration'),
(417284, 'HP:0033302', 'Elevated circulating 4-hydroxyphenylacetic acid concentration', 'XPO:0141922', 'abnormal valine metabolic process', 0.6363636363636364, 9.119292702704945, 2.4089803372708736, 'HP:0004354', 'Abnormal circulating carboxylic acid concentration'),
(417285, 'HP:0033302', 'Elevated circulating 4-hydroxyphenylacetic acid concentration', 'XPO:0141913', 'abnormal L-serine metabolic process', 0.625, 9.119292702704945, 2.387374696018744, 'HP:0004354', 'Abnormal circulating carboxylic acid concentration'),
(417286, 'HP:0033302', 'Elevated circulating 4-hydroxyphenylacetic acid concentration', 'XPO:0141858', 'abnormal serine family amino acid metabolic process', 0.6481481481481481, 9.119292702704945, 2.4311833903840183, 'HP:0004354', 'Abnormal circulating carboxylic acid concentration'),
(417287, 'HP:0033302', 'Elevated circulating 4-hydroxyphenylacetic acid concentration', 'XPO:0141847', 'abnormal arginine metabolic process', 0.6363636363636364, 9.119292702704945, 2.4089803372708736, 'HP:0004354', 'Abnormal circulating carboxylic acid concentration'),
(417288, 'HP:0033302', 'Elevated circulating 4-hydroxyphenylacetic acid concentration', 'XPO:0141869', 'abnormal alpha-amino acid metabolic process', 0.6730769230769231, 9.119292702704945, 2.4774958068530575, 'HP:0004354', 'Abnormal circulating carboxylic acid concentration'),
(417289, 'HP:0033302', 'Elevated circulating 4-hydroxyphenylacetic acid concentration', 'XPO:0141843', 'abnormal alanine metabolic process', 0.6481481481481481, 9.119292702704945, 2.4311833903840183, 'HP:0004354', 'Abnormal circulating carboxylic acid concentration'),
(417290, 'HP:0033302', 'Elevated circulating 4-hydroxyphenylacetic acid concentration', 'XPO:0141887', 'abnormal histidine metabolic process', 0.6363636363636364, 9.119292702704945, 2.4089803372708736, 'HP:0004354', 'Abnormal circulating carboxylic acid concentration'),
(417291, 'HP:0033302', 'Elevated circulating 4-hydroxyphenylacetic acid concentration', 'XPO:0141857', 'abnormal glycine metabolic process', 0.625, 9.119292702704945, 2.387374696018744, 'HP:0004354', 'Abnormal circulating carboxylic acid concentration'),
(417292, 'HP:0033302', 'Elevated circulating 4-hydroxyphenylacetic acid concentration', 'XPO:0141873', 'abnormal tricarboxylic acid metabolic process', 0.7291666666666666, 9.119292702704945, 2.5786593924729613, 'HP:0004354', 'Abnormal circulating carboxylic acid concentration'),
(417293, 'HP:0033302', 'Elevated circulating 4-hydroxyphenylacetic acid concentration', 'XPO:0141912', 'abnormal D-serine metabolic process', 0.625, 9.119292702704945, 2.387374696018744, 'HP:0004354', 'Abnormal circulating carboxylic acid concentration'),
(417294, 'HP:0033302', 'Elevated circulating 4-hydroxyphenylacetic acid concentration', 'XPO:0141918', 'abnormal tyrosine metabolic process', 0.6363636363636364, 9.119292702704945, 2.4089803372708736, 'HP:0004354', 'Abnormal circulating carboxylic acid concentration'),
(417295, 'HP:0033302', 'Elevated circulating 4-hydroxyphenylacetic acid concentration', 'XPO:0141868', 'abnormal asparagine metabolic process', 0.6363636363636364, 9.119292702704945, 2.4089803372708736, 'HP:0004354', 'Abnormal circulating carboxylic acid concentration'),
(417296, 'HP:0033302', 'Elevated circulating 4-hydroxyphenylacetic acid concentration', 'XPO:0141893', 'abnormal isoleucine metabolic process', 0.6363636363636364, 9.119292702704945, 2.4089803372708736, 'HP:0004354', 'Abnormal circulating carboxylic acid concentration'),
(417297, 'HP:0033302', 'Elevated circulating 4-hydroxyphenylacetic acid concentration', 'XPO:0141882', 'abnormal gamma-aminobutyric acid metabolic process', 0.6923076923076923, 10.553838360873003, 2.7030544723709116, 'UPHENO:0050484', 'abnormal monocarboxylic acid metabolic process'),
(417298, 'HP:0033302', 'Elevated circulating 4-hydroxyphenylacetic acid concentration', 'XPO:0141853', 'abnormal glutamate metabolic process', 0.6140350877192983, 9.119292702704945, 2.3663401477056056, 'HP:0004354', 'Abnormal circulating carboxylic acid concentration'),
(417299, 'HP:0033302', 'Elevated circulating 4-hydroxyphenylacetic acid concentration', 'XPO:0141917', 'abnormal tryptophan metabolic process', 0.6363636363636364, 9.119292702704945, 2.4089803372708736, 'HP:0004354', 'Abnormal circulating carboxylic acid concentration'),
(417300, 'HP:0033302', 'Elevated circulating 4-hydroxyphenylacetic acid concentration', 'XPO:0141895', 'abnormal leucine metabolic process', 0.6363636363636364, 9.119292702704945, 2.4089803372708736, 'HP:0004354', 'Abnormal circulating carboxylic acid concentration'),
(417301, 'HP:0007064', 'Progressive language deterioration', 'XPO:0100114', 'abnormal peripheral nervous system', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(417302, 'HP:0007064', 'Progressive language deterioration', 'XPO:0100032', 'abnormal nervous system', 0.4482758620689655, 3.94131651835137, 1.3292091859262085, 'UPHENO:0004523', 'abnormal nervous system'),
(417303, 'HP:0007064', 'Progressive language deterioration', 'XPO:0107253', 'abnormal enteric nervous system', 0.43333333333333335, 3.94131651835137, 1.3068679445984308, 'UPHENO:0004523', 'abnormal nervous system'),
(417304, 'HP:0007064', 'Progressive language deterioration', 'XPO:0100274', 'abnormal sensory system', 0.43333333333333335, 3.94131651835137, 1.3068679445984308, 'UPHENO:0004523', 'abnormal nervous system'),
(417305, 'HP:0007064', 'Progressive language deterioration', 'XPO:0142051', 'abnormal cerebrospinal fluid', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(417306, 'HP:0007064', 'Progressive language deterioration', 'XPO:0100427', 'abnormal olfactory system', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(417307, 'HP:0007064', 'Progressive language deterioration', 'XPO:0100164', 'abnormal neural nucleus', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(417308, 'HP:0007064', 'Progressive language deterioration', 'XPO:0100587', 'abnormal vestibuloauditory system', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(417309, 'HP:0007064', 'Progressive language deterioration', 'XPO:0100273', 'abnormal visual system', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(417310, 'HP:0007064', 'Progressive language deterioration', 'XPO:0100031', 'abnormal central nervous system', 0.43333333333333335, 3.94131651835137, 1.3068679445984308, 'UPHENO:0004523', 'abnormal nervous system'),
(417311, 'HP:0007064', 'Progressive language deterioration', 'XPO:0100642', 'abnormal gustatory system', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(417312, 'HP:0001769', 'Broad foot', 'XPO:0129662', 'increased size of the hindlimb stylopod', 0.4067796610169492, 7.333232559010569, 1.7271392110981598, 'UPHENO:0084767', 'abnormal anatomical entity morphology in the pelvic complex'),
(417313, 'HP:0001769', 'Broad foot', 'XPO:0129792', 'increased size of the zeugopod', 0.41509433962264153, 5.972749669260594, 1.574564885831345, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(417314, 'HP:0001769', 'Broad foot', 'XPO:0129487', 'increased size of the anatomical structure', 0.42105263157894735, 5.972749669260594, 1.585825326448175, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(417315, 'HP:0001769', 'Broad foot', 'XPO:0101837', 'abnormal limb segment morphology', 0.41304347826086957, 5.914846961127896, 1.563038375154302, 'UPHENO:0084763', 'abnormal anatomical entity morphology in the appendage girdle complex'),
(417316, 'HP:0001769', 'Broad foot', 'XPO:0129582', 'increased size of the portion of organism substance', 0.42105263157894735, 5.972749669260594, 1.585825326448175, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(417317, 'HP:0001769', 'Broad foot', 'XPO:0128741', 'decreased size of the interdigital region', 0.44680851063829785, 6.173473740856008, 1.6608313001676343, 'UPHENO:0087006', 'abnormal autopod region morphology'),
(417318, 'HP:0001769', 'Broad foot', 'XPO:0129933', 'increased size of the hindlimb zeugopod', 0.4067796610169492, 7.333232559010569, 1.7271392110981598, 'UPHENO:0084767', 'abnormal anatomical entity morphology in the pelvic complex'),
(417319, 'HP:0001769', 'Broad foot', 'XPO:0141541', 'inverted joint region in hindlimb', 0.40384615384615385, 7.333232559010569, 1.7209002772432245, 'UPHENO:0084767', 'abnormal anatomical entity morphology in the pelvic complex'),
(417320, 'HP:0001769', 'Broad foot', 'XPO:0129982', 'increased size of the anatomical line', 0.42105263157894735, 5.972749669260594, 1.585825326448175, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(417321, 'HP:0001769', 'Broad foot', 'XPO:0129536', 'increased size of the limb segment', 0.44, 5.972749669260594, 1.6211137697504951, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(417322, 'HP:0001769', 'Broad foot', 'XPO:0102018', 'abnormal limb morphology', 0.41304347826086957, 5.914846961127896, 1.563038375154302, 'UPHENO:0084763', 'abnormal anatomical entity morphology in the appendage girdle complex'),
(417323, 'HP:0001769', 'Broad foot', 'XPO:0102484', 'abnormal interdigital region morphology', 0.47619047619047616, 6.173473740856008, 1.7145697420658113, 'UPHENO:0087006', 'abnormal autopod region morphology'),
(417324, 'HP:0001769', 'Broad foot', 'XPO:0103383', 'increased size of the hindlimb', 0.42857142857142855, 7.333232559010569, 1.7727983398744687, 'UPHENO:0084767', 'abnormal anatomical entity morphology in the pelvic complex'),
(417325, 'HP:0001769', 'Broad foot', 'XPO:0102478', 'abnormal hindlimb morphology', 0.42, 7.333232559010569, 1.754980818922087, 'UPHENO:0084767', 'abnormal anatomical entity morphology in the pelvic complex'),
(417326, 'HP:0001769', 'Broad foot', 'XPO:0103754', 'increased size of the foot', 0.4067796610169492, 7.333232559010569, 1.7271392110981598, 'UPHENO:0084767', 'abnormal anatomical entity morphology in the pelvic complex'),
(417327, 'HP:0001769', 'Broad foot', 'XPO:0141578', 'abnormal joint region morphology in the hindlimb', 0.42857142857142855, 7.333232559010569, 1.7727983398744687, 'UPHENO:0084767', 'abnormal anatomical entity morphology in the pelvic complex'),
(417328, 'HP:0001769', 'Broad foot', 'XPO:0140528', 'abnormally necrotic interdigital region', 0.43478260869565216, 6.173473740856008, 1.6383281166370434, 'UPHENO:0087006', 'abnormal autopod region morphology'),
(417329, 'HP:0001769', 'Broad foot', 'XPO:0129777', 'increased size of the limb', 0.43137254901960786, 5.972749669260594, 1.6051418160041069, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(417330, 'HP:0001769', 'Broad foot', 'XPO:0129663', 'increased size of the stylopod', 0.41509433962264153, 5.972749669260594, 1.574564885831345, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(417331, 'HP:0001769', 'Broad foot', 'XPO:0130219', 'increased size of the interdigital region', 0.5111111111111111, 6.173473740856008, 1.7763251456600455, 'UPHENO:0087006', 'abnormal autopod region morphology'),
(417332, 'HP:0001769', 'Broad foot', 'XPO:0129535', 'increased size of the autopod', 0.41509433962264153, 5.972749669260594, 1.574564885831345, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(417333, 'HP:0001769', 'Broad foot', 'XPO:0130763', 'increased size of the interdigital webbing', 0.41818181818181815, 6.173473740856008, 1.6067465492257564, 'UPHENO:0087006', 'abnormal autopod region morphology'),
(417334, 'HP:0010027', 'Broad 1st metacarpal', 'XPO:0115788', 'duplicated forelimb digit 4 in regenerating forelimb', 0.41605839416058393, 7.774297771301195, 1.7984887673971672, 'HP:0005918', 'Abnormal finger phalanx morphology'),
(417335, 'HP:0010027', 'Broad 1st metacarpal', 'XPO:0102746', 'abnormal forelimb digit 2 morphology', 0.40869565217391307, 7.492661022682715, 1.7499194219115835, 'HP:0001167', 'Abnormal finger morphology'),
(417336, 'HP:0010027', 'Broad 1st metacarpal', 'XPO:0115787', 'duplicated forelimb digit 3 in regenerating forelimb', 0.41605839416058393, 7.774297771301195, 1.7984887673971672, 'HP:0005918', 'Abnormal finger phalanx morphology'),
(417337, 'HP:0010027', 'Broad 1st metacarpal', 'XPO:0130664', 'increased size of the forelimb digit 2', 0.4065040650406504, 7.492661022682715, 1.7452212363170925, 'HP:0001167', 'Abnormal finger morphology'),
(417338, 'HP:0010027', 'Broad 1st metacarpal', 'XPO:0102214', 'abnormal forelimb digit morphology', 0.415929203539823, 7.492661022682715, 1.7653375120804229, 'HP:0001167', 'Abnormal finger morphology'),
(417339, 'HP:0010027', 'Broad 1st metacarpal', 'XPO:0130637', 'increased size of the forelimb digit 5', 0.4065040650406504, 7.492661022682715, 1.7452212363170925, 'HP:0001167', 'Abnormal finger morphology'),
(417340, 'HP:0010027', 'Broad 1st metacarpal', 'XPO:0115786', 'duplicated forelimb digit 2 in regenerating forelimb', 0.41605839416058393, 7.774297771301195, 1.7984887673971672, 'HP:0005918', 'Abnormal finger phalanx morphology'),
(417341, 'HP:0010027', 'Broad 1st metacarpal', 'XPO:0129652', 'increased size of the forelimb digit 3', 0.4065040650406504, 7.492661022682715, 1.7452212363170925, 'HP:0001167', 'Abnormal finger morphology'),
(417342, 'HP:0010027', 'Broad 1st metacarpal', 'XPO:0115789', 'duplicated forelimb digit 5 in regenerating forelimb', 0.41605839416058393, 7.774297771301195, 1.7984887673971672, 'HP:0005918', 'Abnormal finger phalanx morphology'),
(417343, 'HP:0010027', 'Broad 1st metacarpal', 'XPO:0102787', 'abnormal forelimb digit 5 morphology', 0.40869565217391307, 7.492661022682715, 1.7499194219115835, 'HP:0001167', 'Abnormal finger morphology'),
(417344, 'HP:0010027', 'Broad 1st metacarpal', 'XPO:0102598', 'abnormal forelimb digit 3 morphology', 0.40869565217391307, 7.492661022682715, 1.7499194219115835, 'HP:0001167', 'Abnormal finger morphology'),
(417345, 'HP:0010027', 'Broad 1st metacarpal', 'XPO:0102529', 'abnormal forelimb digit 4 morphology', 0.40869565217391307, 7.492661022682715, 1.7499194219115835, 'HP:0001167', 'Abnormal finger morphology'),
(417346, 'HP:0010027', 'Broad 1st metacarpal', 'XPO:0103609', 'abnormally increased number of forelimb digit in the regenerating forelimb', 0.4318181818181818, 7.774297771301195, 1.8322344633033256, 'HP:0005918', 'Abnormal finger phalanx morphology'),
(417347, 'HP:0010027', 'Broad 1st metacarpal', 'XPO:0103634', 'abnormally increased number of forelimb digit', 0.4523809523809524, 7.774297771301195, 1.875351761636827, 'HP:0005918', 'Abnormal finger phalanx morphology'),
(417348, 'HP:0010027', 'Broad 1st metacarpal', 'XPO:0103755', 'increased size of the forelimb digit', 0.4166666666666667, 7.492661022682715, 1.7669018345070744, 'HP:0001167', 'Abnormal finger morphology'),
(417349, 'HP:0010027', 'Broad 1st metacarpal', 'XPO:0130624', 'increased size of the forelimb digit 4', 0.4065040650406504, 7.492661022682715, 1.7452212363170925, 'HP:0001167', 'Abnormal finger morphology'),
(417350, 'HP:0006670', 'Impaired myocardial contractility', 'XPO:0100172', 'abnormal stem cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(417351, 'HP:0006670', 'Impaired myocardial contractility', 'XPO:0101206', 'abnormal ischiadic vein', 0.4117647058823529, 5.249153838287537, 1.4701755971154233, 'UPHENO:0080362', 'abnormal cardiovascular system'),
(417352, 'HP:0006670', 'Impaired myocardial contractility', 'XPO:0100980', 'abnormal dorsal longitudinal anastomosing vessel - left branch', 0.4117647058823529, 5.249153838287537, 1.4701755971154233, 'UPHENO:0080362', 'abnormal cardiovascular system'),
(417353, 'HP:0006670', 'Impaired myocardial contractility', 'XPO:0101243', 'abnormal vertebral artery', 0.4117647058823529, 5.249153838287537, 1.4701755971154233, 'UPHENO:0080362', 'abnormal cardiovascular system'),
(417354, 'HP:0006670', 'Impaired myocardial contractility', 'XPO:0101373', 'abnormal oxygen accumulating cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(417355, 'HP:0006670', 'Impaired myocardial contractility', 'XPO:0100981', 'abnormal dorsal longitudinal anastomosing vessel', 0.42424242424242425, 5.249153838287537, 1.4922847414540332, 'UPHENO:0080362', 'abnormal cardiovascular system'),
(417356, 'HP:0006670', 'Impaired myocardial contractility', 'XPO:0100004', 'abnormal cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(417357, 'HP:0006670', 'Impaired myocardial contractility', 'XPO:0100080', 'abnormal aorta', 0.4117647058823529, 5.249153838287537, 1.4701755971154233, 'UPHENO:0080362', 'abnormal cardiovascular system'),
(417358, 'HP:0006670', 'Impaired myocardial contractility', 'XPO:0100026', 'abnormal germ cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(417359, 'HP:0006670', 'Impaired myocardial contractility', 'XPO:0100754', 'abnormal electrically active cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(417360, 'HP:0006670', 'Impaired myocardial contractility', 'XPO:0101535', 'abnormal absorptive cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(417361, 'HP:0006670', 'Impaired myocardial contractility', 'XPO:0100054', 'abnormal blood vessel', 0.4375, 5.249153838287537, 1.5154223187781013, 'UPHENO:0080362', 'abnormal cardiovascular system'),
(417362, 'HP:0006670', 'Impaired myocardial contractility', 'XPO:0100792', 'abnormal capillary', 0.42424242424242425, 5.249153838287537, 1.4922847414540332, 'UPHENO:0080362', 'abnormal cardiovascular system'),
(417363, 'HP:0006670', 'Impaired myocardial contractility', 'XPO:0101557', 'abnormal Jacobsons vein', 0.4117647058823529, 5.249153838287537, 1.4701755971154233, 'UPHENO:0080362', 'abnormal cardiovascular system'),
(417364, 'HP:0006670', 'Impaired myocardial contractility', 'XPO:0100533', 'abnormal melanoblast', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(417365, 'HP:0006670', 'Impaired myocardial contractility', 'XPO:0101333', 'abnormal barrier epithelial cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(417366, 'HP:0006670', 'Impaired myocardial contractility', 'XPO:0101435', 'abnormal paracrine cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(417367, 'HP:0006670', 'Impaired myocardial contractility', 'XPO:0100852', 'abnormal interdigital region', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(417368, 'HP:0006670', 'Impaired myocardial contractility', 'XPO:0100791', 'abnormal multiciliated cell precursor', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(417369, 'HP:0006670', 'Impaired myocardial contractility', 'XPO:0101326', 'abnormal cementoblast', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(417370, 'HP:0006670', 'Impaired myocardial contractility', 'XPO:0100081', 'abnormal anatomical entity in vitro', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(417371, 'HP:0006670', 'Impaired myocardial contractility', 'XPO:0101448', 'abnormal myelin accumulating cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(417372, 'HP:0006670', 'Impaired myocardial contractility', 'XPO:0100780', 'abnormal vascular plexus', 0.42424242424242425, 5.249153838287537, 1.4922847414540332, 'UPHENO:0080362', 'abnormal cardiovascular system'),
(417373, 'HP:0006670', 'Impaired myocardial contractility', 'XPO:0101237', 'abnormal mucus secreting cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(417374, 'HP:0006670', 'Impaired myocardial contractility', 'XPO:0100006', 'abnormal anatomical structure', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(417375, 'HP:0006670', 'Impaired myocardial contractility', 'XPO:0100481', 'abnormal anatomical line', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(417376, 'HP:0006670', 'Impaired myocardial contractility', 'XPO:0101583', 'abnormal truncus arteriosus', 0.42424242424242425, 5.249153838287537, 1.4922847414540332, 'UPHENO:0080362', 'abnormal cardiovascular system'),
(417377, 'HP:0006670', 'Impaired myocardial contractility', 'XPO:0100137', 'abnormal cardinal vein', 0.4117647058823529, 5.249153838287537, 1.4701755971154233, 'UPHENO:0080362', 'abnormal cardiovascular system'),
(417378, 'HP:0006670', 'Impaired myocardial contractility', 'XPO:0100337', 'abnormal zygote', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(417379, 'HP:0006670', 'Impaired myocardial contractility', 'XPO:0101467', 'abnormal alkali secreting cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(417380, 'HP:0006670', 'Impaired myocardial contractility', 'XPO:0101431', 'abnormal ischiadic artery', 0.4117647058823529, 5.249153838287537, 1.4701755971154233, 'UPHENO:0080362', 'abnormal cardiovascular system'),
(417381, 'HP:0006670', 'Impaired myocardial contractility', 'XPO:0100108', 'abnormal cell part', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(417382, 'HP:0006670', 'Impaired myocardial contractility', 'XPO:0101241', 'abnormal nucleate erythrocyte', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(417383, 'HP:0006670', 'Impaired myocardial contractility', 'XPO:0100987', 'abnormal larval aorta', 0.4117647058823529, 5.249153838287537, 1.4701755971154233, 'UPHENO:0080362', 'abnormal cardiovascular system'),
(417384, 'HP:0006670', 'Impaired myocardial contractility', 'XPO:0100522', 'abnormal subinterstitial vein', 0.4117647058823529, 5.249153838287537, 1.4701755971154233, 'UPHENO:0080362', 'abnormal cardiovascular system'),
(417385, 'HP:0006670', 'Impaired myocardial contractility', 'XPO:0100549', 'abnormal mitotic cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(417386, 'HP:0006670', 'Impaired myocardial contractility', 'XPO:0100715', 'abnormal ciliated cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(417387, 'HP:0006670', 'Impaired myocardial contractility', 'XPO:0100933', 'abnormal branchial vein', 0.4117647058823529, 5.249153838287537, 1.4701755971154233, 'UPHENO:0080362', 'abnormal cardiovascular system'),
(417388, 'HP:0006670', 'Impaired myocardial contractility', 'XPO:0100691', 'abnormal keratin accumulating cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(417389, 'HP:0006670', 'Impaired myocardial contractility', 'XPO:0101132', 'abnormal apoptotic cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(417390, 'HP:0006670', 'Impaired myocardial contractility', 'XPO:0100289', 'abnormal chondroblast', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(417391, 'HP:0006670', 'Impaired myocardial contractility', 'XPO:0100653', 'abnormal myoblast', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(417392, 'HP:0006670', 'Impaired myocardial contractility', 'XPO:0100285', 'abnormal progenitor cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(417393, 'HP:0006670', 'Impaired myocardial contractility', 'XPO:0100704', 'abnormal Merkel cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(417394, 'HP:0006670', 'Impaired myocardial contractility', 'XPO:0101297', 'abnormal barrier cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(417395, 'HP:0006670', 'Impaired myocardial contractility', 'XPO:0100802', 'abnormal exocrine cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(417396, 'HP:0006670', 'Impaired myocardial contractility', 'XPO:0101004', 'abnormal acid secreting cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(417397, 'HP:0006670', 'Impaired myocardial contractility', 'XPO:0100638', 'abnormal polar body', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(417398, 'HP:0006670', 'Impaired myocardial contractility', 'XPO:0100477', 'abnormal pericyte', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(417399, 'HP:0006670', 'Impaired myocardial contractility', 'XPO:0101585', 'abnormal dorsal longitudinal anastomosing vessel - right branch', 0.4117647058823529, 5.249153838287537, 1.4701755971154233, 'UPHENO:0080362', 'abnormal cardiovascular system'),
(417400, 'HP:0006670', 'Impaired myocardial contractility', 'XPO:0100344', 'abnormal portion of organism substance', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(417401, 'HP:0006670', 'Impaired myocardial contractility', 'XPO:0100076', 'abnormal artery', 0.42424242424242425, 5.249153838287537, 1.4922847414540332, 'UPHENO:0080362', 'abnormal cardiovascular system'),
(417402, 'HP:0006670', 'Impaired myocardial contractility', 'XPO:0100043', 'abnormal vein', 0.42424242424242425, 5.249153838287537, 1.4922847414540332, 'UPHENO:0080362', 'abnormal cardiovascular system'),
(417403, 'HP:0006670', 'Impaired myocardial contractility', 'XPO:0100789', 'abnormal occipitovertebral artery', 0.4117647058823529, 5.249153838287537, 1.4701755971154233, 'UPHENO:0080362', 'abnormal cardiovascular system'),
(417404, 'HP:0009668', 'Fragmentation of the epiphysis of the proximal phalanx of the thumb', 'XPO:0103609', 'abnormally increased number of forelimb digit in the regenerating forelimb', 0.41304347826086957, 7.774297771301195, 1.7919606559559202, 'HP:0005918', 'Abnormal finger phalanx morphology'),
(417405, 'HP:0009668', 'Fragmentation of the epiphysis of the proximal phalanx of the thumb', 'XPO:0103634', 'abnormally increased number of forelimb digit', 0.4318181818181818, 7.774297771301195, 1.8322344633033256, 'HP:0005918', 'Abnormal finger phalanx morphology'),
(417406, 'HP:0032107', 'Limbal stem cell deficiency', 'XPO:0102513', 'abnormal sclera morphology', 0.47692307692307695, 6.887869297006056, 1.8124524320853552, 'HP:0012372', 'Abnormal eye morphology'),
(417407, 'HP:0032107', 'Limbal stem cell deficiency', 'XPO:0125990', 'absent hyaloid vein', 0.4305555555555556, 6.887869297006056, 1.7220947685207388, 'HP:0012372', 'Abnormal eye morphology'),
(417408, 'HP:0032107', 'Limbal stem cell deficiency', 'XPO:0102082', 'abnormal circumpharyngeal ridge morphology', 0.42, 4.5318002188002176, 1.3796217205799897, 'UPHENO:0087907', 'abnormal head morphology'),
(417409, 'HP:0032107', 'Limbal stem cell deficiency', 'XPO:0103707', 'increased pigmentation in the head', 0.42857142857142855, 4.5318002188002176, 1.3936283915633758, 'UPHENO:0087907', 'abnormal head morphology'),
(417410, 'HP:0032107', 'Limbal stem cell deficiency', 'XPO:0141298', 'abnormal intercanthal region morphology', 0.4375, 4.5318002188002176, 1.4080705222839853, 'UPHENO:0087907', 'abnormal head morphology'),
(417411, 'HP:0032107', 'Limbal stem cell deficiency', 'XPO:0126122', 'absent hyaloid vascular plexus', 0.4246575342465753, 6.887869297006056, 1.7102589253909142, 'HP:0012372', 'Abnormal eye morphology'),
(417412, 'HP:0032107', 'Limbal stem cell deficiency', 'XPO:0141323', 'edematous eye', 0.4696969696969697, 6.887869297006056, 1.7986693238259617, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(417413, 'HP:0032107', 'Limbal stem cell deficiency', 'XPO:0141337', 'increased pigmentation in the eye', 0.4626865671641791, 6.887869297006056, 1.7851959556606887, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(417414, 'HP:0032107', 'Limbal stem cell deficiency', 'XPO:0141343', 'decreased pigmentation in the eye', 0.4626865671641791, 6.887869297006056, 1.7851959556606887, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(417415, 'HP:0032107', 'Limbal stem cell deficiency', 'XPO:0133372', 'eye fused with olfactory epithelium', 0.4626865671641791, 6.887869297006056, 1.7851959556606887, 'HP:0012372', 'Abnormal eye morphology'),
(417416, 'HP:0032107', 'Limbal stem cell deficiency', 'XPO:0103110', 'abnormal lens fiber cell mass morphology', 0.44155844155844154, 9.014833150514745, 1.9951380094746995, 'UPHENO:0021038', 'abnormal anterior segment of eyeball morphology'),
(417417, 'HP:0032107', 'Limbal stem cell deficiency', 'XPO:0141839', 'edematous pharyngeal region', 0.44680851063829785, 4.5318002188002176, 1.422971154406314, 'UPHENO:0087907', 'abnormal head morphology'),
(417418, 'HP:0032107', 'Limbal stem cell deficiency', 'XPO:0129419', 'decreased size of the pupil', 0.44155844155844154, 9.014833150514745, 1.9951380094746995, 'UPHENO:0021038', 'abnormal anterior segment of eyeball morphology'),
(417419, 'HP:0032107', 'Limbal stem cell deficiency', 'XPO:0140914', 'abnormally necrotic intercanthal region', 0.4117647058823529, 4.5318002188002176, 1.3660290568695288, 'UPHENO:0087907', 'abnormal head morphology'),
(417420, 'HP:0032107', 'Limbal stem cell deficiency', 'XPO:0102212', 'abnormal globe morphology', 0.42857142857142855, 6.575878401988876, 1.6787595422967447, 'UPHENO:0087924', 'abnormal camera-type eye morphology'),
(417421, 'HP:0032107', 'Limbal stem cell deficiency', 'XPO:0102572', 'abnormal hatching gland primordium morphology', 0.4117647058823529, 4.5318002188002176, 1.3660290568695288, 'UPHENO:0087907', 'abnormal head morphology'),
(417422, 'HP:0032107', 'Limbal stem cell deficiency', 'XPO:0102734', 'abnormal craniofacial region morphology', 0.42857142857142855, 4.5318002188002176, 1.3936283915633758, 'UPHENO:0087907', 'abnormal head morphology'),
(417423, 'HP:0032107', 'Limbal stem cell deficiency', 'XPO:0128564', 'decreased size of the hyaloid blood vessel', 0.4025974025974026, 6.887869297006056, 1.6652442128423794, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(417424, 'HP:0032107', 'Limbal stem cell deficiency', 'XPO:0141835', 'edematous head', 0.4375, 4.5318002188002176, 1.4080705222839853, 'UPHENO:0087907', 'abnormal head morphology'),
(417425, 'HP:0032107', 'Limbal stem cell deficiency', 'XPO:0130736', 'increased size of the cornea', 0.41975308641975306, 9.014833150514745, 1.9452516645636548, 'UPHENO:0021038', 'abnormal anterior segment of eyeball morphology'),
(417426, 'HP:0032107', 'Limbal stem cell deficiency', 'XPO:0140250', 'abnormally necrotic iris', 0.4473684210526316, 9.014833150514745, 2.0082210218496126, 'UPHENO:0021038', 'abnormal anterior segment of eyeball morphology'),
(417427, 'HP:0032107', 'Limbal stem cell deficiency', 'XPO:0102805', 'abnormal retinal layer morphology', 0.4492753623188406, 6.887869297006056, 1.759133301946505, 'HP:0012372', 'Abnormal eye morphology'),
(417428, 'HP:0032107', 'Limbal stem cell deficiency', 'XPO:0140538', 'abnormally necrotic optic disc', 0.421875, 6.575878401988876, 1.6655925974976766, 'UPHENO:0087924', 'abnormal camera-type eye morphology'),
(417429, 'HP:0032107', 'Limbal stem cell deficiency', 'XPO:0127783', 'abnormally localised hyaloid vascular plexus', 0.44285714285714284, 6.887869297006056, 1.7465228647932265, 'HP:0012372', 'Abnormal eye morphology'),
(417430, 'HP:0032107', 'Limbal stem cell deficiency', 'XPO:0140375', 'abnormally necrotic lens', 0.4857142857142857, 9.014833150514745, 2.0925183976576487, 'UPHENO:0021038', 'abnormal anterior segment of eyeball morphology'),
(417431, 'HP:0032107', 'Limbal stem cell deficiency', 'XPO:0102259', 'abnormal pharyngeal region morphology', 0.4666666666666667, 4.5318002188002176, 1.4542489821577214, 'UPHENO:0087907', 'abnormal head morphology'),
(417432, 'HP:0032107', 'Limbal stem cell deficiency', 'XPO:0130651', 'increased size of the lens epithelium', 0.40476190476190477, 9.014833150514745, 1.910199213986099, 'UPHENO:0021038', 'abnormal anterior segment of eyeball morphology'),
(417433, 'HP:0032107', 'Limbal stem cell deficiency', 'XPO:0140487', 'abnormally necrotic retinal layer', 0.41333333333333333, 6.887869297006056, 1.6873013886368484, 'HP:0012372', 'Abnormal eye morphology'),
(417434, 'HP:0032107', 'Limbal stem cell deficiency', 'XPO:0130539', 'increased size of the ciliary body', 0.4050632911392405, 8.412768222102876, 1.8459966369515974, 'UPHENO:0087597', 'abnormal anterior segment of eyeball morphology'),
(417435, 'HP:0032107', 'Limbal stem cell deficiency', 'XPO:0102862', 'abnormal iris morphology', 0.4788732394366197, 9.014833150514745, 2.077730096467687, 'UPHENO:0021038', 'abnormal anterior segment of eyeball morphology'),
(417436, 'HP:0032107', 'Limbal stem cell deficiency', 'XPO:0141141', 'abnormally necrotic cornea', 0.4533333333333333, 9.014833150514745, 2.021564829919309, 'UPHENO:0021038', 'abnormal anterior segment of eyeball morphology'),
(417437, 'HP:0032107', 'Limbal stem cell deficiency', 'XPO:0102784', 'abnormal retinal progenitor cell region morphology', 0.41333333333333333, 6.887869297006056, 1.6873013886368484, 'HP:0012372', 'Abnormal eye morphology'),
(417438, 'HP:0032107', 'Limbal stem cell deficiency', 'XPO:0101483', 'abnormal nostril', 0.46153846153846156, 5.788671267106304, 1.6345318690598054, 'UPHENO:0087472', 'abnormal face morphology'),
(417439, 'HP:0032107', 'Limbal stem cell deficiency', 'XPO:0130285', 'increased size of the lens transitional zone', 0.4594594594594595, 9.014833150514745, 2.0351782149120803, 'UPHENO:0021038', 'abnormal anterior segment of eyeball morphology'),
(417440, 'HP:0032107', 'Limbal stem cell deficiency', 'XPO:0140391', 'abnormally necrotic central retina', 0.4189189189189189, 6.887869297006056, 1.6986638159319787, 'HP:0012372', 'Abnormal eye morphology'),
(417441, 'HP:0032107', 'Limbal stem cell deficiency', 'XPO:0102831', 'abnormal optic disc morphology', 0.4426229508196721, 6.575878401988876, 1.7060582353834428, 'UPHENO:0087924', 'abnormal camera-type eye morphology'),
(417442, 'HP:0032107', 'Limbal stem cell deficiency', 'XPO:0101359', 'abnormal hyaloid artery', 0.4305555555555556, 6.887869297006056, 1.7220947685207388, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(417443, 'HP:0032107', 'Limbal stem cell deficiency', 'XPO:0100371', 'abnormal hyaloid blood vessel', 0.5535714285714286, 6.887869297006056, 1.9526719249676645, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(417444, 'HP:0032107', 'Limbal stem cell deficiency', 'XPO:0140452', 'abnormally necrotic lens epithelium', 0.4146341463414634, 9.014833150514745, 1.9333539892565992, 'UPHENO:0021038', 'abnormal anterior segment of eyeball morphology'),
(417445, 'HP:0032107', 'Limbal stem cell deficiency', 'XPO:0102342', 'abnormal hyaloid vein morphology', 0.4025974025974026, 6.887869297006056, 1.6652442128423794, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(417446, 'HP:0032107', 'Limbal stem cell deficiency', 'XPO:0128807', 'decreased size of the lens transitional zone', 0.4594594594594595, 9.014833150514745, 2.0351782149120803, 'UPHENO:0021038', 'abnormal anterior segment of eyeball morphology'),
(417447, 'HP:0032107', 'Limbal stem cell deficiency', 'XPO:0130413', 'increased size of the central retina', 0.40789473684210525, 6.887869297006056, 1.6761639640277146, 'HP:0012372', 'Abnormal eye morphology'),
(417448, 'HP:0032107', 'Limbal stem cell deficiency', 'XPO:0130893', 'increased size of the pupil', 0.4473684210526316, 9.014833150514745, 2.0082210218496126, 'UPHENO:0021038', 'abnormal anterior segment of eyeball morphology'),
(417449, 'HP:0032107', 'Limbal stem cell deficiency', 'XPO:0103160', 'abnormal choroid morphology', 0.4153846153846154, 6.575878401988876, 1.652730686114997, 'UPHENO:0087924', 'abnormal camera-type eye morphology'),
(417450, 'HP:0032107', 'Limbal stem cell deficiency', 'XPO:0102117', 'abnormal retina morphology', 0.43661971830985913, 6.887869297006056, 1.734179792355427, 'HP:0012372', 'Abnormal eye morphology'),
(417451, 'HP:0032107', 'Limbal stem cell deficiency', 'XPO:0100329', 'abnormal retinal blood vessel', 0.44285714285714284, 6.887869297006056, 1.7465228647932265, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(417452, 'HP:0032107', 'Limbal stem cell deficiency', 'XPO:0102966', 'abnormal olfactory pit morphology', 0.42105263157894735, 5.788671267106304, 1.561196743002159, 'UPHENO:0087472', 'abnormal face morphology'),
(417453, 'HP:0032107', 'Limbal stem cell deficiency', 'XPO:0100779', 'abnormal optic choroid vascular plexus', 0.543859649122807, 6.887869297006056, 1.9354674316747025, 'HP:0012372', 'Abnormal eye morphology'),
(417454, 'HP:0032107', 'Limbal stem cell deficiency', 'XPO:0102538', 'abnormal lateral nasal prominence morphology', 0.42857142857142855, 4.5318002188002176, 1.3936283915633758, 'UPHENO:0087907', 'abnormal head morphology'),
(417455, 'HP:0032107', 'Limbal stem cell deficiency', 'XPO:0102804', 'abnormal pharyngeal pouch morphology', 0.42857142857142855, 4.5318002188002176, 1.3936283915633758, 'UPHENO:0087907', 'abnormal head morphology'),
(417456, 'HP:0032107', 'Limbal stem cell deficiency', 'XPO:0139722', 'abnormally necrotic hyaloid blood vessel', 0.41333333333333333, 6.887869297006056, 1.6873013886368484, 'HP:0012372', 'Abnormal eye morphology'),
(417457, 'HP:0032107', 'Limbal stem cell deficiency', 'XPO:0140223', 'abnormally necrotic head region', 0.4117647058823529, 4.5318002188002176, 1.3660290568695288, 'UPHENO:0087907', 'abnormal head morphology'),
(417458, 'HP:0032107', 'Limbal stem cell deficiency', 'XPO:0133369', 'eye fused with brain', 0.4626865671641791, 6.887869297006056, 1.7851959556606887, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(417459, 'HP:0032107', 'Limbal stem cell deficiency', 'XPO:0133354', 'fused eyes', 0.4626865671641791, 6.887869297006056, 1.7851959556606887, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(417460, 'HP:0032107', 'Limbal stem cell deficiency', 'XPO:0127230', 'abnormally localised hyaloid blood vessel', 0.47692307692307695, 6.887869297006056, 1.8124524320853552, 'HP:0012372', 'Abnormal eye morphology'),
(417461, 'HP:0032107', 'Limbal stem cell deficiency', 'XPO:0127907', 'abnormally localised optic choroid vascular plexus', 0.45588235294117646, 6.887869297006056, 1.7720208976957377, 'HP:0012372', 'Abnormal eye morphology'),
(417462, 'HP:0032107', 'Limbal stem cell deficiency', 'XPO:0141339', 'decreased pigmentation in the head', 0.42857142857142855, 4.5318002188002176, 1.3936283915633758, 'UPHENO:0087907', 'abnormal head morphology'),
(417463, 'HP:0032107', 'Limbal stem cell deficiency', 'XPO:0102226', 'abnormal Jacobsons organ morphology', 0.4067796610169492, 5.788671267106304, 1.5345076525622334, 'UPHENO:0087472', 'abnormal face morphology'),
(417464, 'HP:0032107', 'Limbal stem cell deficiency', 'XPO:0101817', 'abnormal eye morphology', 0.484375, 6.887869297006056, 1.8265573330003382, 'HP:0012372', 'Abnormal eye morphology'),
(417465, 'HP:0032107', 'Limbal stem cell deficiency', 'XPO:0140192', 'abnormally necrotic retina', 0.40789473684210525, 6.887869297006056, 1.6761639640277146, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(417466, 'HP:0032107', 'Limbal stem cell deficiency', 'XPO:0101634', 'abnormal head morphology', 0.45652173913043476, 4.5318002188002176, 1.4383550734357495, 'UPHENO:0087907', 'abnormal head morphology'),
(417467, 'HP:0032107', 'Limbal stem cell deficiency', 'XPO:0103376', 'increased size of the eye', 0.41333333333333333, 6.887869297006056, 1.6873013886368484, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(417468, 'HP:0032107', 'Limbal stem cell deficiency', 'XPO:0129062', 'decreased size of the ciliary body', 0.4050632911392405, 8.412768222102876, 1.8459966369515974, 'UPHENO:0087597', 'abnormal anterior segment of eyeball morphology'),
(417469, 'HP:0032107', 'Limbal stem cell deficiency', 'XPO:0129388', 'decreased size of the sclera', 0.4305555555555556, 6.887869297006056, 1.7220947685207388, 'HP:0012372', 'Abnormal eye morphology'),
(417470, 'HP:0032107', 'Limbal stem cell deficiency', 'XPO:0102196', 'abnormal central retina morphology', 0.43661971830985913, 6.887869297006056, 1.734179792355427, 'HP:0012372', 'Abnormal eye morphology'),
(417471, 'HP:0032107', 'Limbal stem cell deficiency', 'XPO:0142059', 'abnormal nasal region morphology', 0.44680851063829785, 4.5318002188002176, 1.422971154406314, 'UPHENO:0087907', 'abnormal head morphology'),
(417472, 'HP:0032107', 'Limbal stem cell deficiency', 'XPO:0100420', 'abnormal choana', 0.4444444444444444, 5.788671267106304, 1.6039771773253444, 'UPHENO:0087472', 'abnormal face morphology'),
(417473, 'HP:0032107', 'Limbal stem cell deficiency', 'XPO:0128467', 'decreased size of the lens', 0.4657534246575342, 9.014833150514745, 2.0490703776514145, 'UPHENO:0021038', 'abnormal anterior segment of eyeball morphology'),
(417474, 'HP:0032107', 'Limbal stem cell deficiency', 'XPO:0103336', 'decreased size of the eye', 0.41333333333333333, 6.887869297006056, 1.6873013886368484, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(417475, 'HP:0032107', 'Limbal stem cell deficiency', 'XPO:0129532', 'increased size of the iris', 0.4358974358974359, 9.014833150514745, 1.982307406875276, 'UPHENO:0021038', 'abnormal anterior segment of eyeball morphology'),
(417476, 'HP:0032107', 'Limbal stem cell deficiency', 'XPO:0128935', 'decreased size of the central retina', 0.40789473684210525, 6.887869297006056, 1.6761639640277146, 'HP:0012372', 'Abnormal eye morphology'),
(417477, 'HP:0032107', 'Limbal stem cell deficiency', 'XPO:0100710', 'abnormal hyaloid vein', 0.5344827586206896, 6.887869297006056, 1.9187098224803423, 'HP:0012372', 'Abnormal eye morphology'),
(417478, 'HP:0032107', 'Limbal stem cell deficiency', 'XPO:0102550', 'abnormal lens morphology', 0.5230769230769231, 9.014833150514745, 2.1715089653103203, 'UPHENO:0021038', 'abnormal anterior segment of eyeball morphology'),
(417479, 'HP:0032107', 'Limbal stem cell deficiency', 'XPO:0103022', 'abnormal ciliary body morphology', 0.4507042253521127, 8.412768222102876, 1.9472211442488363, 'UPHENO:0087597', 'abnormal anterior segment of eyeball morphology'),
(417480, 'HP:0032107', 'Limbal stem cell deficiency', 'XPO:0139715', 'abnormally necrotic head', 0.4117647058823529, 4.5318002188002176, 1.3660290568695288, 'UPHENO:0087907', 'abnormal head morphology'),
(417481, 'HP:0032107', 'Limbal stem cell deficiency', 'XPO:0115526', 'abnormally incomplete structure of head', 0.44680851063829785, 4.5318002188002176, 1.422971154406314, 'UPHENO:0087907', 'abnormal head morphology'),
(417482, 'HP:0032107', 'Limbal stem cell deficiency', 'XPO:0101173', 'abnormal retinal layer', 0.4117647058823529, 6.02624522851634, 1.5752444553449358, 'HP:0000478', 'Abnormality of the eye'),
(417483, 'HP:0032107', 'Limbal stem cell deficiency', 'XPO:0103186', 'abnormal peripheral retina morphology', 0.4189189189189189, 6.887869297006056, 1.6986638159319787, 'HP:0012372', 'Abnormal eye morphology'),
(417484, 'HP:0032107', 'Limbal stem cell deficiency', 'XPO:0102947', 'abnormal hyaloid vascular plexus morphology', 0.40789473684210525, 6.887869297006056, 1.6761639640277146, 'HP:0012372', 'Abnormal eye morphology'),
(417485, 'HP:0032107', 'Limbal stem cell deficiency', 'XPO:0103358', 'decreased size of the pharyngeal region', 0.42, 4.5318002188002176, 1.3796217205799897, 'UPHENO:0087907', 'abnormal head morphology'),
(417486, 'HP:0032107', 'Limbal stem cell deficiency', 'XPO:0140218', 'abnormally necrotic sclera', 0.44285714285714284, 6.887869297006056, 1.7465228647932265, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(417487, 'HP:0032107', 'Limbal stem cell deficiency', 'XPO:0125589', 'absent hyaloid blood vessel', 0.45588235294117646, 6.887869297006056, 1.7720208976957377, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(417488, 'HP:0032107', 'Limbal stem cell deficiency', 'XPO:0141638', 'neoplastic eye', 0.4626865671641791, 6.887869297006056, 1.7851959556606887, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(417489, 'HP:0032107', 'Limbal stem cell deficiency', 'XPO:0140335', 'abnormally necrotic pharyngeal region', 0.4375, 4.5318002188002176, 1.4080705222839853, 'UPHENO:0087907', 'abnormal head morphology'),
(417490, 'HP:0032107', 'Limbal stem cell deficiency', 'XPO:0133371', 'eye fused with olfactory pit', 0.4626865671641791, 6.887869297006056, 1.7851959556606887, 'HP:0012372', 'Abnormal eye morphology'),
(417491, 'HP:0032107', 'Limbal stem cell deficiency', 'XPO:0103101', 'abnormal medial nasal prominence morphology', 0.42857142857142855, 4.5318002188002176, 1.3936283915633758, 'UPHENO:0087907', 'abnormal head morphology'),
(417492, 'HP:0032107', 'Limbal stem cell deficiency', 'XPO:0101823', 'abnormal lens epithelium morphology', 0.4594594594594595, 9.014833150514745, 2.0351782149120803, 'UPHENO:0021038', 'abnormal anterior segment of eyeball morphology'),
(417493, 'HP:0032107', 'Limbal stem cell deficiency', 'XPO:0127645', 'abnormally localised hyaloid vein', 0.4492753623188406, 6.887869297006056, 1.759133301946505, 'HP:0012372', 'Abnormal eye morphology'),
(417494, 'HP:0032107', 'Limbal stem cell deficiency', 'XPO:0130122', 'increased size of the retinal layer', 0.40789473684210525, 6.887869297006056, 1.6761639640277146, 'HP:0012372', 'Abnormal eye morphology'),
(417495, 'HP:0032107', 'Limbal stem cell deficiency', 'XPO:0140473', 'abnormally necrotic lens transitional zone', 0.4722222222222222, 9.014833150514745, 2.0632509646910697, 'UPHENO:0021038', 'abnormal anterior segment of eyeball morphology'),
(417496, 'HP:0032107', 'Limbal stem cell deficiency', 'XPO:0103739', 'increased size of the pharyngeal region', 0.42, 4.5318002188002176, 1.3796217205799897, 'UPHENO:0087907', 'abnormal head morphology'),
(417497, 'HP:0032107', 'Limbal stem cell deficiency', 'XPO:0130048', 'increased size of the optic disc', 0.4090909090909091, 6.575878401988876, 1.640162209521029, 'UPHENO:0087924', 'abnormal camera-type eye morphology'),
(417498, 'HP:0032107', 'Limbal stem cell deficiency', 'XPO:0128052', 'decreased size of the iris', 0.4358974358974359, 9.014833150514745, 1.982307406875276, 'UPHENO:0021038', 'abnormal anterior segment of eyeball morphology'),
(417499, 'HP:0032107', 'Limbal stem cell deficiency', 'XPO:0140799', 'abnormally necrotic ciliary body', 0.4155844155844156, 8.412768222102876, 1.869816933560547, 'UPHENO:0087597', 'abnormal anterior segment of eyeball morphology'),
(417500, 'HP:0032107', 'Limbal stem cell deficiency', 'XPO:0103048', 'abnormal cornea morphology', 0.4927536231884058, 9.014833150514745, 2.1076270299450734, 'UPHENO:0021038', 'abnormal anterior segment of eyeball morphology'),
(417501, 'HP:0032107', 'Limbal stem cell deficiency', 'XPO:0103210', 'abnormal pupil morphology', 0.4788732394366197, 9.014833150514745, 2.077730096467687, 'UPHENO:0021038', 'abnormal anterior segment of eyeball morphology'),
(417502, 'HP:0032107', 'Limbal stem cell deficiency', 'XPO:0115423', 'abnormally incomplete structure of eye', 0.47692307692307695, 6.887869297006056, 1.8124524320853552, 'HP:0012372', 'Abnormal eye morphology'),
(417503, 'HP:0032107', 'Limbal stem cell deficiency', 'XPO:0102003', 'abnormal hyaloid blood vessel morphology', 0.4492753623188406, 6.887869297006056, 1.759133301946505, 'HP:0012372', 'Abnormal eye morphology'),
(417504, 'HP:0032107', 'Limbal stem cell deficiency', 'XPO:0102476', 'abnormal lens transitional zone morphology', 0.5074626865671642, 9.014833150514745, 2.138852834936276, 'UPHENO:0021038', 'abnormal anterior segment of eyeball morphology'),
(417505, 'HP:0032107', 'Limbal stem cell deficiency', 'XPO:0129260', 'decreased size of the cornea', 0.41975308641975306, 9.014833150514745, 1.9452516645636548, 'UPHENO:0021038', 'abnormal anterior segment of eyeball morphology'),
(417506, 'HP:0032107', 'Limbal stem cell deficiency', 'XPO:0139731', 'abnormally necrotic eye', 0.43661971830985913, 6.887869297006056, 1.734179792355427, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(417507, 'HP:0032107', 'Limbal stem cell deficiency', 'XPO:0102505', 'abnormal retinal stem cell region morphology', 0.41333333333333333, 6.887869297006056, 1.6873013886368484, 'HP:0012372', 'Abnormal eye morphology'),
(417508, 'HP:0032107', 'Limbal stem cell deficiency', 'XPO:0128643', 'decreased size of the retinal layer', 0.40789473684210525, 6.887869297006056, 1.6761639640277146, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(417509, 'HP:0032107', 'Limbal stem cell deficiency', 'XPO:0129175', 'decreased size of the lens epithelium', 0.40476190476190477, 9.014833150514745, 1.910199213986099, 'UPHENO:0021038', 'abnormal anterior segment of eyeball morphology'),
(417510, 'HP:0032107', 'Limbal stem cell deficiency', 'XPO:0128568', 'decreased size of the optic disc', 0.4090909090909091, 6.575878401988876, 1.640162209521029, 'UPHENO:0087924', 'abnormal camera-type eye morphology'),
(417511, 'HP:0032107', 'Limbal stem cell deficiency', 'XPO:0129947', 'increased size of the lens', 0.4657534246575342, 9.014833150514745, 2.0490703776514145, 'UPHENO:0021038', 'abnormal anterior segment of eyeball morphology'),
(417512, 'HP:0032107', 'Limbal stem cell deficiency', 'XPO:0126243', 'absent optic choroid vascular plexus', 0.4246575342465753, 6.887869297006056, 1.7102589253909142, 'HP:0012372', 'Abnormal eye morphology'),
(417513, 'HP:0032107', 'Limbal stem cell deficiency', 'XPO:0130863', 'increased size of the sclera', 0.4305555555555556, 6.887869297006056, 1.7220947685207388, 'HP:0012372', 'Abnormal eye morphology'),
(417514, 'HP:0032107', 'Limbal stem cell deficiency', 'XPO:0101315', 'abnormal hyaloid vascular plexus', 0.5344827586206896, 6.887869297006056, 1.9187098224803423, 'HP:0012372', 'Abnormal eye morphology'),
(417515, 'HP:0032107', 'Limbal stem cell deficiency', 'XPO:0130044', 'increased size of the hyaloid blood vessel', 0.4025974025974026, 6.887869297006056, 1.6652442128423794, 'HP:0012372', 'Abnormal eye morphology'),
(417516, 'HP:0032107', 'Limbal stem cell deficiency', 'XPO:0115417', 'abnormally wholly ventralized eye', 0.43661971830985913, 6.887869297006056, 1.734179792355427, 'HP:0012372', 'Abnormal eye morphology'),
(417517, 'HP:0006665', 'Coat hanger sign of ribs', 'XPO:0102542', 'abnormal vacuolated notochordal tissue morphology', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(417518, 'HP:0006665', 'Coat hanger sign of ribs', 'XPO:0141703', 'abnormally necrotic posterior notochord', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(417519, 'HP:0006665', 'Coat hanger sign of ribs', 'XPO:0100584', 'abnormal vertebral column', 0.5, 6.272837960958401, 1.770993783297728, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(417520, 'HP:0006665', 'Coat hanger sign of ribs', 'XPO:0101957', 'abnormal axial skeleton morphology', 0.44680851063829785, 6.211345574613551, 1.665917784661915, 'UPHENO:0087089', 'abnormal axial skeleton plus cranial skeleton morphology'),
(417521, 'HP:0006665', 'Coat hanger sign of ribs', 'XPO:0128890', 'decreased size of the elastica externa', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(417522, 'HP:0006665', 'Coat hanger sign of ribs', 'XPO:0128580', 'decreased size of the postcranial axial skeleton', 0.4107142857142857, 6.272837960958401, 1.6050994245019483, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(417523, 'HP:0006665', 'Coat hanger sign of ribs', 'XPO:0140683', 'abnormally necrotic flexural organ', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(417524, 'HP:0006665', 'Coat hanger sign of ribs', 'XPO:0140019', 'abnormally necrotic skeletal system', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(417525, 'HP:0006665', 'Coat hanger sign of ribs', 'XPO:0139774', 'abnormally necrotic elastica externa', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(417526, 'HP:0006665', 'Coat hanger sign of ribs', 'XPO:0141699', 'abnormally necrotic anterior notochord', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(417527, 'HP:0006665', 'Coat hanger sign of ribs', 'XPO:0130368', 'increased size of the elastica externa', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(417528, 'HP:0006665', 'Coat hanger sign of ribs', 'XPO:0102144', 'abnormal cranial skeleton morphology', 0.4375, 6.211345574613551, 1.6484731386629958, 'UPHENO:0087089', 'abnormal axial skeleton plus cranial skeleton morphology'),
(417529, 'HP:0006665', 'Coat hanger sign of ribs', 'XPO:0140510', 'abnormally necrotic postcranial axial skeleton', 0.42592592592592593, 6.272837960958401, 1.6345532468244968, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(417530, 'HP:0006665', 'Coat hanger sign of ribs', 'XPO:0130060', 'increased size of the postcranial axial skeleton', 0.4107142857142857, 6.272837960958401, 1.6050994245019483, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(417531, 'HP:0006665', 'Coat hanger sign of ribs', 'XPO:0102461', 'abnormal postcranial axial skeleton morphology', 0.4791666666666667, 6.272837960958401, 1.7337055275601352, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(417532, 'HP:0006665', 'Coat hanger sign of ribs', 'XPO:0102093', 'abnormal craniofacial skeleton morphology', 0.42, 6.211345574613551, 1.61516721776344, 'UPHENO:0087089', 'abnormal axial skeleton plus cranial skeleton morphology'),
(417533, 'HP:0006665', 'Coat hanger sign of ribs', 'XPO:0102567', 'abnormal skeleton morphology', 0.45454545454545453, 4.638757693672553, 1.452076521536181, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(417534, 'HP:0006665', 'Coat hanger sign of ribs', 'XPO:0102605', 'abnormal dermal skeleton morphology', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(417535, 'HP:0006665', 'Coat hanger sign of ribs', 'XPO:0102980', 'abnormal perichordal tissue morphology', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(417536, 'HP:0006665', 'Coat hanger sign of ribs', 'XPO:0140559', 'abnormally necrotic articular system', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(417537, 'HP:0006665', 'Coat hanger sign of ribs', 'XPO:0140432', 'abnormally necrotic skeleton', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(417538, 'HP:0006665', 'Coat hanger sign of ribs', 'XPO:0141719', 'abnormal anterior notochord morphology', 0.45454545454545453, 4.638757693672553, 1.452076521536181, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(417539, 'HP:0006665', 'Coat hanger sign of ribs', 'XPO:0102272', 'abnormal notochordal sheath morphology', 0.45454545454545453, 4.638757693672553, 1.452076521536181, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(417540, 'HP:0006665', 'Coat hanger sign of ribs', 'XPO:0126886', 'abnormally localised vertebral column', 0.41818181818181815, 6.272837960958401, 1.6196255072310737, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(417541, 'HP:0006665', 'Coat hanger sign of ribs', 'XPO:0100226', 'abnormal vertebral element', 0.4423076923076923, 6.272837960958401, 1.6656903922192745, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(417542, 'HP:0006665', 'Coat hanger sign of ribs', 'XPO:0102130', 'abnormal endoskeleton morphology', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(417543, 'HP:0006665', 'Coat hanger sign of ribs', 'XPO:0101860', 'abnormal skeletal subdivision morphology', 0.4444444444444444, 4.638757693672553, 1.4358516936218344, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(417544, 'HP:0006665', 'Coat hanger sign of ribs', 'XPO:0102217', 'abnormal elastica externa morphology', 0.47619047619047616, 4.638757693672553, 1.4862477031377266, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(417545, 'HP:0006665', 'Coat hanger sign of ribs', 'XPO:0101982', 'abnormal appendicular skeleton morphology', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(417546, 'HP:0006665', 'Coat hanger sign of ribs', 'XPO:0102010', 'abnormal perichondrium morphology', 0.4444444444444444, 4.638757693672553, 1.4358516936218344, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(417547, 'HP:0006665', 'Coat hanger sign of ribs', 'XPO:0102216', 'abnormal vertebral column morphology', 0.4423076923076923, 6.272837960958401, 1.6656903922192745, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(417548, 'HP:0006665', 'Coat hanger sign of ribs', 'XPO:0140350', 'abnormally necrotic notochordal sheath', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(417549, 'HP:0006665', 'Coat hanger sign of ribs', 'XPO:0100693', 'abnormal vertebral centrum', 0.4339622641509434, 6.272837960958401, 1.6499015013598524, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(417550, 'HP:0006665', 'Coat hanger sign of ribs', 'XPO:0102054', 'abnormal notochord morphology', 0.45454545454545453, 4.638757693672553, 1.452076521536181, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(417551, 'HP:0006665', 'Coat hanger sign of ribs', 'XPO:0102514', 'abnormal perichondrial cell morphology', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(417552, 'HP:0006665', 'Coat hanger sign of ribs', 'XPO:0102806', 'abnormal articular system morphology', 0.46511627906976744, 4.638757693672553, 1.4688640910537754, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(417553, 'HP:0006665', 'Coat hanger sign of ribs', 'XPO:0141723', 'abnormal posterior notochord morphology', 0.45454545454545453, 4.638757693672553, 1.452076521536181, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(417554, 'HP:0006665', 'Coat hanger sign of ribs', 'XPO:0102097', 'abnormal skeletal system morphology', 0.47619047619047616, 4.638757693672553, 1.4862477031377266, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(417555, 'HP:0006665', 'Coat hanger sign of ribs', 'XPO:0129832', 'increased size of the skeletal system', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(417556, 'HP:0006665', 'Coat hanger sign of ribs', 'XPO:0107372', 'abnormal flexural organ morphology', 0.45454545454545453, 4.638757693672553, 1.452076521536181, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(417557, 'HP:0006665', 'Coat hanger sign of ribs', 'XPO:0128352', 'decreased size of the skeletal system', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(417558, 'HP:0032076', 'Abnormal male urethral meatus morphology', 'XPO:0101669', 'abnormal gonad morphology', 0.40816326530612246, 6.723205497167461, 1.656552295898908, 'UPHENO:0087547', 'abnormal reproductive system morphology'),
(417559, 'HP:0032076', 'Abnormal male urethral meatus morphology', 'XPO:0129028', 'decreased size of the male genitalia', 0.4444444444444444, 8.414388317771037, 1.9338376718927501, 'HP:0010461', 'Abnormality of the male genitalia'),
(417560, 'HP:0032076', 'Abnormal male urethral meatus morphology', 'XPO:0102133', 'abnormal urogenital system morphology', 0.4146341463414634, 5.4478002382576385, 1.5029451091868848, 'HP:0000119', 'Abnormality of the genitourinary system'),
(417561, 'HP:0032076', 'Abnormal male urethral meatus morphology', 'XPO:0102397', 'abnormal male genitalia morphology', 0.5217391304347826, 8.414388317771037, 2.095260280741859, 'HP:0010461', 'Abnormality of the male genitalia'),
(417562, 'HP:0032076', 'Abnormal male urethral meatus morphology', 'XPO:0126762', 'abnormally localised male genitalia', 0.4897959183673469, 8.414388317771037, 2.030106660646711, 'HP:0010461', 'Abnormality of the male genitalia'),
(417563, 'HP:0032076', 'Abnormal male urethral meatus morphology', 'XPO:0139866', 'abnormally necrotic male genitalia', 0.46153846153846156, 8.414388317771037, 1.9706759852830318, 'HP:0010461', 'Abnormality of the male genitalia'),
(417564, 'HP:0032076', 'Abnormal male urethral meatus morphology', 'XPO:0100666', 'abnormal primary spermatogonium', 0.43636363636363634, 8.414388317771037, 1.916176683951214, 'HP:0010461', 'Abnormality of the male genitalia'),
(417565, 'HP:0032076', 'Abnormal male urethral meatus morphology', 'XPO:0100414', 'abnormal testis', 0.48, 8.414388317771037, 2.009703060785373, 'HP:0010461', 'Abnormality of the male genitalia'),
(417566, 'HP:0032076', 'Abnormal male urethral meatus morphology', 'XPO:0125139', 'absent male genitalia', 0.48, 8.414388317771037, 2.009703060785373, 'HP:0010461', 'Abnormality of the male genitalia'),
(417567, 'HP:0032076', 'Abnormal male urethral meatus morphology', 'XPO:0139867', 'abnormally necrotic genital system', 0.46808510638297873, 7.005035523447265, 1.810787894318205, 'UPHENO:0020950', 'abnormal reproductive system morphology'),
(417568, 'HP:0032076', 'Abnormal male urethral meatus morphology', 'XPO:0140723', 'abnormally necrotic polar body', 0.43137254901960786, 7.005035523447265, 1.7383267902561792, 'HP:0012243', 'Abnormal reproductive system morphology'),
(417569, 'HP:0032076', 'Abnormal male urethral meatus morphology', 'XPO:0140839', 'abnormally necrotic female genitalia', 0.4074074074074074, 7.005035523447265, 1.689349981917436, 'UPHENO:0020950', 'abnormal reproductive system morphology'),
(417570, 'HP:0032076', 'Abnormal male urethral meatus morphology', 'XPO:0101262', 'abnormal oviduct', 0.4782608695652174, 7.005035523447265, 1.8303645486020337, 'HP:0012243', 'Abnormal reproductive system morphology'),
(417571, 'HP:0032076', 'Abnormal male urethral meatus morphology', 'XPO:0101232', 'abnormal female genitalia', 0.5238095238095238, 7.005035523447265, 1.915542826930714, 'UPHENO:0020950', 'abnormal reproductive system morphology'),
(417572, 'HP:0032076', 'Abnormal male urethral meatus morphology', 'XPO:0102864', 'abnormal female genitalia morphology', 0.4583333333333333, 7.005035523447265, 1.7918262420167856, 'HP:0012243', 'Abnormal reproductive system morphology'),
(417573, 'HP:0032076', 'Abnormal male urethral meatus morphology', 'XPO:0101948', 'abnormal gamete morphology', 0.40816326530612246, 6.723205497167461, 1.656552295898908, 'UPHENO:0087547', 'abnormal reproductive system morphology'),
(417574, 'HP:0032076', 'Abnormal male urethral meatus morphology', 'XPO:0126964', 'abnormally localised female genitalia', 0.43137254901960786, 7.005035523447265, 1.7383267902561792, 'HP:0012243', 'Abnormal reproductive system morphology'),
(417575, 'HP:0032076', 'Abnormal male urethral meatus morphology', 'XPO:0128384', 'decreased size of the genital system', 0.4489795918367347, 7.005035523447265, 1.7734480511475887, 'HP:0012243', 'Abnormal reproductive system morphology'),
(417576, 'HP:0032076', 'Abnormal male urethral meatus morphology', 'XPO:0125335', 'absent female genitalia', 0.4230769230769231, 7.005035523447265, 1.7215309684419309, 'HP:0012243', 'Abnormal reproductive system morphology'),
(417577, 'HP:0032076', 'Abnormal male urethral meatus morphology', 'XPO:0129864', 'increased size of the genital system', 0.4489795918367347, 7.005035523447265, 1.7734480511475887, 'UPHENO:0020950', 'abnormal reproductive system morphology'),
(417578, 'HP:0032076', 'Abnormal male urethral meatus morphology', 'XPO:0130505', 'increased size of the male genitalia', 0.4444444444444444, 8.414388317771037, 1.9338376718927501, 'HP:0010461', 'Abnormality of the male genitalia'),
(417579, 'HP:0032076', 'Abnormal male urethral meatus morphology', 'XPO:0101752', 'abnormal genital system morphology', 0.5238095238095238, 7.005035523447265, 1.915542826930714, 'UPHENO:0020950', 'abnormal reproductive system morphology'),
(417580, 'HP:0032076', 'Abnormal male urethral meatus morphology', 'XPO:0101372', 'abnormal seminiferous tubule', 0.4528301886792453, 8.414388317771037, 1.9519961704769546, 'HP:0010461', 'Abnormality of the male genitalia'),
(417581, 'HP:0032076', 'Abnormal male urethral meatus morphology', 'XPO:0102270', 'abnormal polar body morphology', 0.46808510638297873, 7.005035523447265, 1.810787894318205, 'HP:0012243', 'Abnormal reproductive system morphology'),
(417582, 'HP:0032076', 'Abnormal male urethral meatus morphology', 'XPO:0100765', 'abnormal male genitalia', 0.6, 8.414388317771037, 2.246916329252743, 'HP:0010461', 'Abnormality of the male genitalia'),
(417583, 'HP:0032076', 'Abnormal male urethral meatus morphology', 'XPO:0102894', 'abnormal oviduct morphology', 0.4230769230769231, 7.005035523447265, 1.7215309684419309, 'UPHENO:0020950', 'abnormal reproductive system morphology'),
(417584, 'HP:0100861', 'Sclerotic vertebral body', 'XPO:0103218', 'abnormal joint morphology', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(417585, 'HP:0100861', 'Sclerotic vertebral body', 'XPO:0101982', 'abnormal appendicular skeleton morphology', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(417586, 'HP:0100861', 'Sclerotic vertebral body', 'XPO:0141708', 'decreased size of the posterior notochord', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(417587, 'HP:0100861', 'Sclerotic vertebral body', 'XPO:0100226', 'abnormal vertebral element', 0.5208333333333334, 8.05344015541032, 2.048047870764469, 'UPHENO:0002813', 'abnormal vertebral column'),
(417588, 'HP:0100861', 'Sclerotic vertebral body', 'XPO:0141704', 'decreased size of the anterior notochord', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(417589, 'HP:0100861', 'Sclerotic vertebral body', 'XPO:0140103', 'abnormally necrotic vertebral column', 0.49056603773584906, 8.361863005979023, 2.025350834530429, 'UPHENO:0076695', 'abnormal vertebral column morphology'),
(417590, 'HP:0100861', 'Sclerotic vertebral body', 'XPO:0139774', 'abnormally necrotic elastica externa', 0.4444444444444444, 4.638757693672553, 1.4358516936218344, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(417591, 'HP:0100861', 'Sclerotic vertebral body', 'XPO:0102093', 'abnormal craniofacial skeleton morphology', 0.4375, 6.211345574613551, 1.6484731386629958, 'UPHENO:0087089', 'abnormal axial skeleton plus cranial skeleton morphology'),
(417592, 'HP:0100861', 'Sclerotic vertebral body', 'XPO:0130908', 'increased size of the notochordal sheath', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(417593, 'HP:0100861', 'Sclerotic vertebral body', 'XPO:0141699', 'abnormally necrotic anterior notochord', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(417594, 'HP:0100861', 'Sclerotic vertebral body', 'XPO:0102514', 'abnormal perichondrial cell morphology', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(417595, 'HP:0100861', 'Sclerotic vertebral body', 'XPO:0141709', 'increased size of the anterior notochord', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(417596, 'HP:0100861', 'Sclerotic vertebral body', 'XPO:0103078', 'abnormal transverse process morphology', 0.4307692307692308, 8.748525470353618, 1.941287095519169, 'HP:0003468', 'Abnormal vertebral morphology'),
(417597, 'HP:0100861', 'Sclerotic vertebral body', 'XPO:0140852', 'abnormally necrotic vertebral centrum', 0.40625, 8.361863005979023, 1.843097079965941, 'UPHENO:0076695', 'abnormal vertebral column morphology'),
(417598, 'HP:0100861', 'Sclerotic vertebral body', 'XPO:0128709', 'decreased size of the flexural organ', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(417599, 'HP:0100861', 'Sclerotic vertebral body', 'XPO:0102272', 'abnormal notochordal sheath morphology', 0.47619047619047616, 4.638757693672553, 1.4862477031377266, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(417600, 'HP:0100861', 'Sclerotic vertebral body', 'XPO:0139917', 'abnormally necrotic notochord', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(417601, 'HP:0100861', 'Sclerotic vertebral body', 'XPO:0141703', 'abnormally necrotic posterior notochord', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(417602, 'HP:0100861', 'Sclerotic vertebral body', 'XPO:0102702', 'abnormal rib morphology', 0.4375, 8.748525470353618, 1.9563946159401757, 'HP:0003468', 'Abnormal vertebral morphology'),
(417603, 'HP:0100861', 'Sclerotic vertebral body', 'XPO:0130188', 'increased size of the flexural organ', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(417604, 'HP:0100861', 'Sclerotic vertebral body', 'XPO:0139795', 'abnormally necrotic vertebral element', 0.4126984126984127, 8.361863005979023, 1.8576672440911264, 'UPHENO:0076695', 'abnormal vertebral column morphology'),
(417605, 'HP:0100861', 'Sclerotic vertebral body', 'XPO:0129434', 'decreased size of the notochordal sheath', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(417606, 'HP:0100861', 'Sclerotic vertebral body', 'XPO:0127548', 'abnormally localised vertebral element', 0.423728813559322, 8.05344015541032, 1.8472884566637167, 'UPHENO:0002813', 'abnormal vertebral column'),
(417607, 'HP:0100861', 'Sclerotic vertebral body', 'XPO:0102828', 'abnormal occipital region morphology', 0.4107142857142857, 6.272837960958401, 1.6050994245019483, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(417608, 'HP:0100861', 'Sclerotic vertebral body', 'XPO:0129832', 'increased size of the skeletal system', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(417609, 'HP:0100861', 'Sclerotic vertebral body', 'XPO:0102113', 'abnormal anatomical line morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(417610, 'HP:0100861', 'Sclerotic vertebral body', 'XPO:0141723', 'abnormal posterior notochord morphology', 0.47619047619047616, 4.638757693672553, 1.4862477031377266, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(417611, 'HP:0100861', 'Sclerotic vertebral body', 'XPO:0100693', 'abnormal vertebral centrum', 0.5102040816326531, 8.05344015541032, 2.0270416962841815, 'UPHENO:0002813', 'abnormal vertebral column'),
(417612, 'HP:0100861', 'Sclerotic vertebral body', 'XPO:0139771', 'abnormally necrotic skeletal subdivision', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(417613, 'HP:0100861', 'Sclerotic vertebral body', 'XPO:0128306', 'decreased size of the articular system', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(417614, 'HP:0100861', 'Sclerotic vertebral body', 'XPO:0103152', 'abnormal otic region morphology', 0.40350877192982454, 6.272837960958401, 1.5909573036826314, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(417615, 'HP:0100861', 'Sclerotic vertebral body', 'XPO:0102728', 'abnormal tendon morphology', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(417616, 'HP:0100861', 'Sclerotic vertebral body', 'XPO:0102097', 'abnormal skeletal system morphology', 0.5, 4.638757693672553, 1.5229507040072823, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(417617, 'HP:0100861', 'Sclerotic vertebral body', 'XPO:0101858', 'abnormal vertebral element morphology', 0.4727272727272727, 8.361863005979023, 1.9881852765111048, 'UPHENO:0076695', 'abnormal vertebral column morphology'),
(417618, 'HP:0100861', 'Sclerotic vertebral body', 'XPO:0101713', 'abnormal anatomical entity in vitro morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(417619, 'HP:0100861', 'Sclerotic vertebral body', 'XPO:0102130', 'abnormal endoskeleton morphology', 0.4444444444444444, 4.638757693672553, 1.4358516936218344, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(417620, 'HP:0100861', 'Sclerotic vertebral body', 'XPO:0100253', 'abnormal vertebra', 0.423728813559322, 8.05344015541032, 1.8472884566637167, 'UPHENO:0002813', 'abnormal vertebral column'),
(417621, 'HP:0100861', 'Sclerotic vertebral body', 'XPO:0126787', 'abnormally localised vertebral centrum', 0.4166666666666667, 8.05344015541032, 1.8318297040812228, 'UPHENO:0002813', 'abnormal vertebral column'),
(417622, 'HP:0100861', 'Sclerotic vertebral body', 'XPO:0102351', 'abnormal sphenoid region morphology', 0.40350877192982454, 6.272837960958401, 1.5909573036826314, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(417623, 'HP:0100861', 'Sclerotic vertebral body', 'XPO:0139889', 'abnormally necrotic cranial skeleton', 0.40384615384615385, 6.211345574613551, 1.5838017617482976, 'UPHENO:0087089', 'abnormal axial skeleton plus cranial skeleton morphology'),
(417624, 'HP:0100861', 'Sclerotic vertebral body', 'XPO:0102217', 'abnormal elastica externa morphology', 0.5, 4.638757693672553, 1.5229507040072823, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(417625, 'HP:0100861', 'Sclerotic vertebral body', 'XPO:0102806', 'abnormal articular system morphology', 0.4878048780487805, 4.638757693672553, 1.5042634845863214, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(417626, 'HP:0100861', 'Sclerotic vertebral body', 'XPO:0102564', 'abnormal olfactory region morphology', 0.40350877192982454, 6.272837960958401, 1.5909573036826314, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(417627, 'HP:0100861', 'Sclerotic vertebral body', 'XPO:0140019', 'abnormally necrotic skeletal system', 0.4444444444444444, 4.638757693672553, 1.4358516936218344, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(417628, 'HP:0100861', 'Sclerotic vertebral body', 'XPO:0100895', 'abnormal presacral vertebra', 0.4166666666666667, 8.05344015541032, 1.8318297040812228, 'UPHENO:0002813', 'abnormal vertebral column'),
(417629, 'HP:0100861', 'Sclerotic vertebral body', 'XPO:0140043', 'abnormally necrotic perichondrium', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(417630, 'HP:0100861', 'Sclerotic vertebral body', 'XPO:0128184', 'decreased size of the skeleton', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(417631, 'HP:0100861', 'Sclerotic vertebral body', 'XPO:0102216', 'abnormal vertebral column morphology', 0.5531914893617021, 8.361863005979023, 2.15074671919221, 'UPHENO:0076695', 'abnormal vertebral column morphology'),
(417632, 'HP:0100861', 'Sclerotic vertebral body', 'XPO:0140559', 'abnormally necrotic articular system', 0.43478260869565216, 4.638757693672553, 1.4201588541997616, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(417633, 'HP:0100861', 'Sclerotic vertebral body', 'XPO:0128352', 'decreased size of the skeletal system', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(417634, 'HP:0100861', 'Sclerotic vertebral body', 'XPO:0102980', 'abnormal perichordal tissue morphology', 0.43478260869565216, 4.638757693672553, 1.4201588541997616, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(417635, 'HP:0100861', 'Sclerotic vertebral body', 'XPO:0101957', 'abnormal axial skeleton morphology', 0.4666666666666667, 6.211345574613551, 1.702535736723214, 'UPHENO:0087089', 'abnormal axial skeleton plus cranial skeleton morphology'),
(417636, 'HP:0100861', 'Sclerotic vertebral body', 'XPO:0141719', 'abnormal anterior notochord morphology', 0.47619047619047616, 4.638757693672553, 1.4862477031377266, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(417637, 'HP:0100861', 'Sclerotic vertebral body', 'XPO:0101860', 'abnormal skeletal subdivision morphology', 0.46511627906976744, 4.638757693672553, 1.4688640910537754, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(417638, 'HP:0100861', 'Sclerotic vertebral body', 'XPO:0139998', 'abnormally necrotic axial skeleton', 0.4117647058823529, 6.211345574613551, 1.599253852164941, 'UPHENO:0087089', 'abnormal axial skeleton plus cranial skeleton morphology'),
(417639, 'HP:0100861', 'Sclerotic vertebral body', 'XPO:0140510', 'abnormally necrotic postcranial axial skeleton', 0.4423076923076923, 6.272837960958401, 1.6656903922192745, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(417640, 'HP:0100861', 'Sclerotic vertebral body', 'XPO:0100927', 'abnormal sacral vertebra', 0.4166666666666667, 8.05344015541032, 1.8318297040812228, 'UPHENO:0002813', 'abnormal vertebral column'),
(417641, 'HP:0100861', 'Sclerotic vertebral body', 'XPO:0140350', 'abnormally necrotic notochordal sheath', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(417642, 'HP:0100861', 'Sclerotic vertebral body', 'XPO:0102054', 'abnormal notochord morphology', 0.47619047619047616, 4.638757693672553, 1.4862477031377266, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(417643, 'HP:0100861', 'Sclerotic vertebral body', 'XPO:0128227', 'decreased size of the vertebral column', 0.4727272727272727, 8.361863005979023, 1.9881852765111048, 'UPHENO:0076695', 'abnormal vertebral column morphology'),
(417644, 'HP:0100861', 'Sclerotic vertebral body', 'XPO:0102010', 'abnormal perichondrium morphology', 0.46511627906976744, 4.638757693672553, 1.4688640910537754, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(417645, 'HP:0100861', 'Sclerotic vertebral body', 'XPO:0102325', 'abnormal vertebral centrum morphology', 0.4642857142857143, 8.361863005979023, 1.9703536582274415, 'UPHENO:0076695', 'abnormal vertebral column morphology'),
(417646, 'HP:0100861', 'Sclerotic vertebral body', 'XPO:0102401', 'abnormal neurocranium morphology', 0.40350877192982454, 6.272837960958401, 1.5909573036826314, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(417647, 'HP:0100861', 'Sclerotic vertebral body', 'XPO:0129664', 'increased size of the skeleton', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(417648, 'HP:0100861', 'Sclerotic vertebral body', 'XPO:0141713', 'increased size of the posterior notochord', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(417649, 'HP:0100861', 'Sclerotic vertebral body', 'XPO:0100252', 'abnormal caudal vertebra', 0.4032258064516129, 8.05344015541032, 1.8020418700394085, 'UPHENO:0002813', 'abnormal vertebral column'),
(417650, 'HP:0100861', 'Sclerotic vertebral body', 'XPO:0102164', 'abnormal mandibular mesenchyme morphology', 0.4117647058823529, 6.211345574613551, 1.599253852164941, 'UPHENO:0087089', 'abnormal axial skeleton plus cranial skeleton morphology'),
(417651, 'HP:0100861', 'Sclerotic vertebral body', 'XPO:0102144', 'abnormal cranial skeleton morphology', 0.45652173913043476, 6.211345574613551, 1.6839282300806968, 'UPHENO:0087089', 'abnormal axial skeleton plus cranial skeleton morphology'),
(417652, 'HP:0100861', 'Sclerotic vertebral body', 'XPO:0103116', 'abnormal bone marrow morphology', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(417653, 'HP:0100861', 'Sclerotic vertebral body', 'XPO:0101638', 'abnormal anatomical structure morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(417654, 'HP:0100861', 'Sclerotic vertebral body', 'XPO:0101976', 'abnormal portion of organism substance morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(417655, 'HP:0100861', 'Sclerotic vertebral body', 'XPO:0102461', 'abnormal postcranial axial skeleton morphology', 0.5, 6.272837960958401, 1.770993783297728, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(417656, 'HP:0100861', 'Sclerotic vertebral body', 'XPO:0129786', 'increased size of the articular system', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(417657, 'HP:0100861', 'Sclerotic vertebral body', 'XPO:0102542', 'abnormal vacuolated notochordal tissue morphology', 0.43478260869565216, 4.638757693672553, 1.4201588541997616, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(417658, 'HP:0100861', 'Sclerotic vertebral body', 'XPO:0141248', 'abnormally necrotic transverse process', 0.4057971014492754, 8.748525470353618, 1.884177878498911, 'HP:0003468', 'Abnormal vertebral morphology'),
(417659, 'HP:0100861', 'Sclerotic vertebral body', 'XPO:0101680', 'abnormal skeletal element morphology', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(417660, 'HP:0100861', 'Sclerotic vertebral body', 'XPO:0129707', 'increased size of the vertebral column', 0.4727272727272727, 8.361863005979023, 1.9881852765111048, 'UPHENO:0076695', 'abnormal vertebral column morphology'),
(417661, 'HP:0100861', 'Sclerotic vertebral body', 'XPO:0128890', 'decreased size of the elastica externa', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(417662, 'HP:0100861', 'Sclerotic vertebral body', 'XPO:0125260', 'absent vertebral column', 0.46296296296296297, 8.05344015541032, 1.9309180501496346, 'UPHENO:0002813', 'abnormal vertebral column'),
(417663, 'HP:0100861', 'Sclerotic vertebral body', 'XPO:0107372', 'abnormal flexural organ morphology', 0.47619047619047616, 4.638757693672553, 1.4862477031377266, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(417664, 'HP:0100861', 'Sclerotic vertebral body', 'XPO:0130060', 'increased size of the postcranial axial skeleton', 0.42592592592592593, 6.272837960958401, 1.6345532468244968, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(417665, 'HP:0100861', 'Sclerotic vertebral body', 'XPO:0140683', 'abnormally necrotic flexural organ', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(417666, 'HP:0100861', 'Sclerotic vertebral body', 'XPO:0126886', 'abnormally localised vertebral column', 0.49019607843137253, 8.05344015541032, 1.9868982817607654, 'UPHENO:0002813', 'abnormal vertebral column'),
(417667, 'HP:0100861', 'Sclerotic vertebral body', 'XPO:0101446', 'abnormal transverse process', 0.4098360655737705, 8.05344015541032, 1.816752660002781, 'UPHENO:0002813', 'abnormal vertebral column'),
(417668, 'HP:0100861', 'Sclerotic vertebral body', 'XPO:0140806', 'abnormally necrotic rib', 0.4117647058823529, 8.748525470353618, 1.8979815639790685, 'HP:0003468', 'Abnormal vertebral morphology'),
(417669, 'HP:0100861', 'Sclerotic vertebral body', 'XPO:0102567', 'abnormal skeleton morphology', 0.47619047619047616, 4.638757693672553, 1.4862477031377266, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(417670, 'HP:0100861', 'Sclerotic vertebral body', 'XPO:0101226', 'abnormal postsacral vertebra', 0.4166666666666667, 8.05344015541032, 1.8318297040812228, 'UPHENO:0002813', 'abnormal vertebral column'),
(417671, 'HP:0100861', 'Sclerotic vertebral body', 'XPO:0130368', 'increased size of the elastica externa', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(417672, 'HP:0100861', 'Sclerotic vertebral body', 'XPO:0100584', 'abnormal vertebral column', 0.5952380952380952, 8.05344015541032, 2.1894552697464333, 'UPHENO:0002813', 'abnormal vertebral column'),
(417673, 'HP:0100861', 'Sclerotic vertebral body', 'XPO:0102605', 'abnormal dermal skeleton morphology', 0.4444444444444444, 4.638757693672553, 1.4358516936218344, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(417674, 'HP:0100861', 'Sclerotic vertebral body', 'XPO:0140432', 'abnormally necrotic skeleton', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(417675, 'HP:0100861', 'Sclerotic vertebral body', 'XPO:0128580', 'decreased size of the postcranial axial skeleton', 0.42592592592592593, 6.272837960958401, 1.6345532468244968, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(417676, 'HP:0100861', 'Sclerotic vertebral body', 'XPO:0101070', 'abnormal rib', 0.4098360655737705, 8.05344015541032, 1.816752660002781, 'UPHENO:0002813', 'abnormal vertebral column'),
(417677, 'HP:0041149', 'Fractured navicular bone of pes', 'XPO:0103072', 'abnormal tarsus morphology', 0.4117647058823529, 11.854497839006713, 2.2093582362445408, 'UPHENO:0088165', 'abnormal tarsal region morphology'),
(417678, 'HP:0040183', 'Encopresis', 'XPO:0100152', 'abnormal alimentary system', 0.42857142857142855, 5.05060299610679, 1.471238981671103, 'HP:0025031', 'Abnormality of the digestive system'),
(417679, 'HP:0040183', 'Encopresis', 'XPO:0115391', 'abnormally undifferentiated alimentary system', 0.4166666666666667, 5.05060299610679, 1.45066119926208, 'HP:0025031', 'Abnormality of the digestive system'),
(417680, 'HP:0040183', 'Encopresis', 'XPO:0100493', 'abnormal liver and biliary system', 0.4166666666666667, 5.05060299610679, 1.45066119926208, 'HP:0025031', 'Abnormality of the digestive system'),
(417681, 'HP:0040183', 'Encopresis', 'XPO:0100890', 'abnormal pharyngeal cavity', 0.40540540540540543, 5.05060299610679, 1.4309233924911664, 'HP:0025031', 'Abnormality of the digestive system'),
(417682, 'HP:0040183', 'Encopresis', 'XPO:0107288', 'abnormal larval alimentary system', 0.4166666666666667, 5.05060299610679, 1.45066119926208, 'HP:0025031', 'Abnormality of the digestive system'),
(417683, 'HP:0040183', 'Encopresis', 'XPO:0142054', 'abnormal digestive tract', 0.40540540540540543, 5.05060299610679, 1.4309233924911664, 'HP:0025031', 'Abnormality of the digestive system'),
(417684, 'HP:0004307', 'Abnormal anatomic location of the heart', 'XPO:0141328', 'edematous circulatory system', 0.4722222222222222, 5.9590888072311134, 1.6775023573665249, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(417685, 'HP:0004307', 'Abnormal anatomic location of the heart', 'XPO:0140104', 'abnormally necrotic circulating cell', 0.40476190476190477, 5.9590888072311134, 1.5530653998657664, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(417686, 'HP:0004307', 'Abnormal anatomic location of the heart', 'XPO:0102178', 'abnormal whole organism morphology', 0.4074074074074074, 2.485033483301678, 1.006191357919822, 'UPHENO:0076692', 'abnormal anatomical entity morphology'),
(417687, 'HP:0004307', 'Abnormal anatomic location of the heart', 'XPO:0101435', 'abnormal paracrine cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(417688, 'HP:0004307', 'Abnormal anatomic location of the heart', 'XPO:0100054', 'abnormal blood vessel', 0.4375, 5.249153838287537, 1.5154223187781013, 'UPHENO:0080362', 'abnormal cardiovascular system'),
(417689, 'HP:0004307', 'Abnormal anatomic location of the heart', 'XPO:0100852', 'abnormal interdigital region', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(417690, 'HP:0004307', 'Abnormal anatomic location of the heart', 'XPO:0100933', 'abnormal branchial vein', 0.4117647058823529, 5.249153838287537, 1.4701755971154233, 'UPHENO:0080362', 'abnormal cardiovascular system'),
(417691, 'HP:0004307', 'Abnormal anatomic location of the heart', 'XPO:0100344', 'abnormal portion of organism substance', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(417692, 'HP:0004307', 'Abnormal anatomic location of the heart', 'XPO:0100337', 'abnormal zygote', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(417693, 'HP:0004307', 'Abnormal anatomic location of the heart', 'XPO:0100549', 'abnormal mitotic cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(417694, 'HP:0004307', 'Abnormal anatomic location of the heart', 'XPO:0100802', 'abnormal exocrine cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(417695, 'HP:0004307', 'Abnormal anatomic location of the heart', 'XPO:0101694', 'abnormal anatomical space morphology', 0.4074074074074074, 2.485033483301678, 1.006191357919822, 'UPHENO:0076692', 'abnormal anatomical entity morphology'),
(417696, 'HP:0004307', 'Abnormal anatomic location of the heart', 'XPO:0101431', 'abnormal ischiadic artery', 0.4117647058823529, 5.249153838287537, 1.4701755971154233, 'UPHENO:0080362', 'abnormal cardiovascular system'),
(417697, 'HP:0004307', 'Abnormal anatomic location of the heart', 'XPO:0128481', 'decreased size of the circulatory system', 0.4146341463414634, 5.9590888072311134, 1.57189112236161, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(417698, 'HP:0004307', 'Abnormal anatomic location of the heart', 'XPO:0100638', 'abnormal polar body', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(417699, 'HP:0004307', 'Abnormal anatomic location of the heart', 'XPO:0139990', 'abnormally necrotic cardiovascular system', 0.4358974358974359, 5.9590888072311134, 1.6116921329326988, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(417700, 'HP:0004307', 'Abnormal anatomic location of the heart', 'XPO:0102233', 'abnormal vascular endothelium morphology', 0.40476190476190477, 5.9590888072311134, 1.5530653998657664, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(417701, 'HP:0004307', 'Abnormal anatomic location of the heart', 'XPO:0107345', 'abnormal anatomical axis morphology', 0.4074074074074074, 2.485033483301678, 1.006191357919822, 'UPHENO:0076692', 'abnormal anatomical entity morphology'),
(417702, 'HP:0004307', 'Abnormal anatomic location of the heart', 'XPO:0141316', 'abnormal anatomical region morphology', 0.4074074074074074, 2.485033483301678, 1.006191357919822, 'UPHENO:0076692', 'abnormal anatomical entity morphology'),
(417703, 'HP:0004307', 'Abnormal anatomic location of the heart', 'XPO:0128032', 'decreased size of the cardiovascular system', 0.4146341463414634, 5.9590888072311134, 1.57189112236161, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(417704, 'HP:0004307', 'Abnormal anatomic location of the heart', 'XPO:0100004', 'abnormal cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(417705, 'HP:0004307', 'Abnormal anatomic location of the heart', 'XPO:0101585', 'abnormal dorsal longitudinal anastomosing vessel - right branch', 0.4117647058823529, 5.249153838287537, 1.4701755971154233, 'UPHENO:0080362', 'abnormal cardiovascular system'),
(417706, 'HP:0004307', 'Abnormal anatomic location of the heart', 'XPO:0100076', 'abnormal artery', 0.42424242424242425, 5.249153838287537, 1.4922847414540332, 'UPHENO:0080362', 'abnormal cardiovascular system'),
(417707, 'HP:0004307', 'Abnormal anatomic location of the heart', 'XPO:0141283', 'abnormal atrioventricular valve morphology', 0.40425531914893614, 7.414388317771038, 1.7312729177384698, 'UPHENO:0076810', 'abnormal heart morphology'),
(417708, 'HP:0004307', 'Abnormal anatomic location of the heart', 'XPO:0100172', 'abnormal stem cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(417709, 'HP:0004307', 'Abnormal anatomic location of the heart', 'XPO:0100533', 'abnormal melanoblast', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(417710, 'HP:0004307', 'Abnormal anatomic location of the heart', 'XPO:0101713', 'abnormal anatomical entity in vitro morphology', 0.44, 2.485033483301678, 1.0456647324323118, 'UPHENO:0076692', 'abnormal anatomical entity morphology'),
(417711, 'HP:0004307', 'Abnormal anatomic location of the heart', 'XPO:0101243', 'abnormal vertebral artery', 0.4117647058823529, 5.249153838287537, 1.4701755971154233, 'UPHENO:0080362', 'abnormal cardiovascular system'),
(417712, 'HP:0004307', 'Abnormal anatomic location of the heart', 'XPO:0103024', 'abnormal sinus venosus morphology', 0.41304347826086957, 7.414388317771038, 1.74998992567069, 'UPHENO:0076810', 'abnormal heart morphology'),
(417713, 'HP:0004307', 'Abnormal anatomic location of the heart', 'XPO:0101900', 'abnormal circulatory system morphology', 0.5151515151515151, 5.9590888072311134, 1.752094069383132, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(417714, 'HP:0004307', 'Abnormal anatomic location of the heart', 'XPO:0101004', 'abnormal acid secreting cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(417715, 'HP:0004307', 'Abnormal anatomic location of the heart', 'XPO:0102113', 'abnormal anatomical line morphology', 0.44, 2.485033483301678, 1.0456647324323118, 'UPHENO:0076692', 'abnormal anatomical entity morphology'),
(417716, 'HP:0004307', 'Abnormal anatomic location of the heart', 'XPO:0100285', 'abnormal progenitor cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(417717, 'HP:0004307', 'Abnormal anatomic location of the heart', 'XPO:0101297', 'abnormal barrier cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(417718, 'HP:0004307', 'Abnormal anatomic location of the heart', 'XPO:0140144', 'abnormally necrotic portion of organism substance', 0.4074074074074074, 2.485033483301678, 1.006191357919822, 'UPHENO:0076692', 'abnormal anatomical entity morphology'),
(417719, 'HP:0004307', 'Abnormal anatomic location of the heart', 'XPO:0100981', 'abnormal dorsal longitudinal anastomosing vessel', 0.42424242424242425, 5.249153838287537, 1.4922847414540332, 'UPHENO:0080362', 'abnormal cardiovascular system'),
(417720, 'HP:0004307', 'Abnormal anatomic location of the heart', 'XPO:0140269', 'abnormally necrotic anatomical line', 0.4074074074074074, 2.485033483301678, 1.006191357919822, 'UPHENO:0076692', 'abnormal anatomical entity morphology'),
(417721, 'HP:0004307', 'Abnormal anatomic location of the heart', 'XPO:0100792', 'abnormal capillary', 0.42424242424242425, 5.249153838287537, 1.4922847414540332, 'UPHENO:0080362', 'abnormal cardiovascular system'),
(417722, 'HP:0004307', 'Abnormal anatomic location of the heart', 'XPO:0101636', 'abnormal cell morphology', 0.40625, 2.485033483301678, 1.004761092295729, 'UPHENO:0076692', 'abnormal anatomical entity morphology'),
(417723, 'HP:0004307', 'Abnormal anatomic location of the heart', 'XPO:0101740', 'abnormal cell part morphology', 0.41935483870967744, 2.485033483301678, 1.0208382906112619, 'UPHENO:0076692', 'abnormal anatomical entity morphology'),
(417724, 'HP:0004307', 'Abnormal anatomic location of the heart', 'XPO:0102773', 'abnormal Keller explant morphology', 0.4074074074074074, 2.485033483301678, 1.006191357919822, 'UPHENO:0076692', 'abnormal anatomical entity morphology'),
(417725, 'HP:0004307', 'Abnormal anatomic location of the heart', 'XPO:0101770', 'abnormal trunk vasculature morphology', 0.425, 5.9590888072311134, 1.5914184688739863, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(417726, 'HP:0004307', 'Abnormal anatomic location of the heart', 'XPO:0102800', 'abnormal circulating cell morphology', 0.4473684210526316, 5.9590888072311134, 1.6327608981732116, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(417727, 'HP:0004307', 'Abnormal anatomic location of the heart', 'XPO:0129961', 'increased size of the circulatory system', 0.4146341463414634, 5.9590888072311134, 1.57189112236161, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(417728, 'HP:0004307', 'Abnormal anatomic location of the heart', 'XPO:0100780', 'abnormal vascular plexus', 0.42424242424242425, 5.249153838287537, 1.4922847414540332, 'UPHENO:0080362', 'abnormal cardiovascular system'),
(417729, 'HP:0004307', 'Abnormal anatomic location of the heart', 'XPO:0100715', 'abnormal ciliated cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(417730, 'HP:0004307', 'Abnormal anatomic location of the heart', 'XPO:0101237', 'abnormal mucus secreting cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(417731, 'HP:0004307', 'Abnormal anatomic location of the heart', 'XPO:0102649', 'abnormal outflow tract morphology', 0.41304347826086957, 7.414388317771038, 1.74998992567069, 'UPHENO:0076810', 'abnormal heart morphology'),
(417732, 'HP:0004307', 'Abnormal anatomic location of the heart', 'XPO:0100081', 'abnormal anatomical entity in vitro', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(417733, 'HP:0004307', 'Abnormal anatomic location of the heart', 'XPO:0101890', 'abnormal organ part morphology', 0.4074074074074074, 2.485033483301678, 1.006191357919822, 'UPHENO:0076692', 'abnormal anatomical entity morphology'),
(417734, 'HP:0004307', 'Abnormal anatomic location of the heart', 'XPO:0129512', 'increased size of the cardiovascular system', 0.4146341463414634, 5.9590888072311134, 1.57189112236161, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(417735, 'HP:0004307', 'Abnormal anatomic location of the heart', 'XPO:0101686', 'abnormal blood vessel morphology', 0.4146341463414634, 5.9590888072311134, 1.57189112236161, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(417736, 'HP:0004307', 'Abnormal anatomic location of the heart', 'XPO:0100980', 'abnormal dorsal longitudinal anastomosing vessel - left branch', 0.4117647058823529, 5.249153838287537, 1.4701755971154233, 'UPHENO:0080362', 'abnormal cardiovascular system'),
(417737, 'HP:0004307', 'Abnormal anatomic location of the heart', 'XPO:0139718', 'abnormally necrotic anatomical structure', 0.4074074074074074, 2.485033483301678, 1.006191357919822, 'UPHENO:0076692', 'abnormal anatomical entity morphology'),
(417738, 'HP:0004307', 'Abnormal anatomic location of the heart', 'XPO:0102532', 'abnormal angioblast morphology', 0.4473684210526316, 5.9590888072311134, 1.6327608981732116, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(417739, 'HP:0004307', 'Abnormal anatomic location of the heart', 'XPO:0100108', 'abnormal cell part', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(417740, 'HP:0004307', 'Abnormal anatomic location of the heart', 'XPO:0101206', 'abnormal ischiadic vein', 0.4117647058823529, 5.249153838287537, 1.4701755971154233, 'UPHENO:0080362', 'abnormal cardiovascular system'),
(417741, 'HP:0004307', 'Abnormal anatomic location of the heart', 'XPO:0100289', 'abnormal chondroblast', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(417742, 'HP:0004307', 'Abnormal anatomic location of the heart', 'XPO:0100043', 'abnormal vein', 0.42424242424242425, 5.249153838287537, 1.4922847414540332, 'UPHENO:0080362', 'abnormal cardiovascular system'),
(417743, 'HP:0004307', 'Abnormal anatomic location of the heart', 'XPO:0100522', 'abnormal subinterstitial vein', 0.4117647058823529, 5.249153838287537, 1.4701755971154233, 'UPHENO:0080362', 'abnormal cardiovascular system'),
(417744, 'HP:0004307', 'Abnormal anatomic location of the heart', 'XPO:0101557', 'abnormal Jacobsons vein', 0.4117647058823529, 5.249153838287537, 1.4701755971154233, 'UPHENO:0080362', 'abnormal cardiovascular system'),
(417745, 'HP:0004307', 'Abnormal anatomic location of the heart', 'XPO:0101995', 'abnormal cardiovascular system morphology', 0.5151515151515151, 5.9590888072311134, 1.752094069383132, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(417746, 'HP:0004307', 'Abnormal anatomic location of the heart', 'XPO:0100080', 'abnormal aorta', 0.4117647058823529, 5.249153838287537, 1.4701755971154233, 'UPHENO:0080362', 'abnormal cardiovascular system'),
(417747, 'HP:0004307', 'Abnormal anatomic location of the heart', 'XPO:0100789', 'abnormal occipitovertebral artery', 0.4117647058823529, 5.249153838287537, 1.4701755971154233, 'UPHENO:0080362', 'abnormal cardiovascular system'),
(417748, 'HP:0004307', 'Abnormal anatomic location of the heart', 'XPO:0100987', 'abnormal larval aorta', 0.4117647058823529, 5.249153838287537, 1.4701755971154233, 'UPHENO:0080362', 'abnormal cardiovascular system'),
(417749, 'HP:0004307', 'Abnormal anatomic location of the heart', 'XPO:0140420', 'abnormally necrotic bulbous arteriosis', 0.4146341463414634, 5.9590888072311134, 1.57189112236161, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(417750, 'HP:0004307', 'Abnormal anatomic location of the heart', 'XPO:0101448', 'abnormal myelin accumulating cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(417751, 'HP:0004307', 'Abnormal anatomic location of the heart', 'XPO:0100006', 'abnormal anatomical structure', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(417752, 'HP:0004307', 'Abnormal anatomic location of the heart', 'XPO:0102601', 'abnormal disaggregated/reaggregated ectoderm treated with activin morphology', 0.4074074074074074, 2.485033483301678, 1.006191357919822, 'UPHENO:0076692', 'abnormal anatomical entity morphology'),
(417753, 'HP:0004307', 'Abnormal anatomic location of the heart', 'XPO:0101535', 'abnormal absorptive cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(417754, 'HP:0004307', 'Abnormal anatomic location of the heart', 'XPO:0101583', 'abnormal truncus arteriosus', 0.42424242424242425, 5.249153838287537, 1.4922847414540332, 'UPHENO:0080362', 'abnormal cardiovascular system'),
(417755, 'HP:0004307', 'Abnormal anatomic location of the heart', 'XPO:0101326', 'abnormal cementoblast', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(417756, 'HP:0004307', 'Abnormal anatomic location of the heart', 'XPO:0139811', 'abnormally necrotic circulatory system', 0.4358974358974359, 5.9590888072311134, 1.6116921329326988, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(417757, 'HP:0004307', 'Abnormal anatomic location of the heart', 'XPO:0103201', 'abnormal activin-induced ectoderm morphology', 0.4074074074074074, 2.485033483301678, 1.006191357919822, 'UPHENO:0076692', 'abnormal anatomical entity morphology'),
(417758, 'HP:0004307', 'Abnormal anatomic location of the heart', 'XPO:0101132', 'abnormal apoptotic cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(417759, 'HP:0004307', 'Abnormal anatomic location of the heart', 'XPO:0100137', 'abnormal cardinal vein', 0.4117647058823529, 5.249153838287537, 1.4701755971154233, 'UPHENO:0080362', 'abnormal cardiovascular system'),
(417760, 'HP:0004307', 'Abnormal anatomic location of the heart', 'XPO:0100477', 'abnormal pericyte', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(417761, 'HP:0004307', 'Abnormal anatomic location of the heart', 'XPO:0101333', 'abnormal barrier epithelial cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(417762, 'HP:0004307', 'Abnormal anatomic location of the heart', 'XPO:0101638', 'abnormal anatomical structure morphology', 0.44, 2.485033483301678, 1.0456647324323118, 'UPHENO:0076692', 'abnormal anatomical entity morphology'),
(417763, 'HP:0004307', 'Abnormal anatomic location of the heart', 'XPO:0102742', 'abnormal cell-free extract morphology', 0.4074074074074074, 2.485033483301678, 1.006191357919822, 'UPHENO:0076692', 'abnormal anatomical entity morphology'),
(417764, 'HP:0004307', 'Abnormal anatomic location of the heart', 'XPO:0100691', 'abnormal keratin accumulating cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(417765, 'HP:0004307', 'Abnormal anatomic location of the heart', 'XPO:0101373', 'abnormal oxygen accumulating cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(417766, 'HP:0004307', 'Abnormal anatomic location of the heart', 'XPO:0101976', 'abnormal portion of organism substance morphology', 0.44, 2.485033483301678, 1.0456647324323118, 'UPHENO:0076692', 'abnormal anatomical entity morphology'),
(417767, 'HP:0004307', 'Abnormal anatomic location of the heart', 'XPO:0101467', 'abnormal alkali secreting cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(417768, 'HP:0004307', 'Abnormal anatomic location of the heart', 'XPO:0100791', 'abnormal multiciliated cell precursor', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(417769, 'HP:0004307', 'Abnormal anatomic location of the heart', 'XPO:0100704', 'abnormal Merkel cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(417770, 'HP:0004307', 'Abnormal anatomic location of the heart', 'XPO:0100653', 'abnormal myoblast', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(417771, 'HP:0004307', 'Abnormal anatomic location of the heart', 'XPO:0141112', 'abnormally necrotic angioblast', 0.40476190476190477, 5.9590888072311134, 1.5530653998657664, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(417772, 'HP:0004307', 'Abnormal anatomic location of the heart', 'XPO:0101919', 'abnormal heart primordium morphology', 0.4473684210526316, 5.9590888072311134, 1.6327608981732116, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(417773, 'HP:0004307', 'Abnormal anatomic location of the heart', 'XPO:0101241', 'abnormal nucleate erythrocyte', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(417774, 'HP:0004307', 'Abnormal anatomic location of the heart', 'XPO:0100754', 'abnormal electrically active cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(417775, 'HP:0004307', 'Abnormal anatomic location of the heart', 'XPO:0102935', 'abnormal bulbous arteriosis morphology', 0.4722222222222222, 5.9590888072311134, 1.6775023573665249, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(417776, 'HP:0004307', 'Abnormal anatomic location of the heart', 'XPO:0100026', 'abnormal germ cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(417777, 'HP:0004307', 'Abnormal anatomic location of the heart', 'XPO:0100481', 'abnormal anatomical line', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(417778, 'HP:0006740', 'Transitional cell carcinoma of the bladder', 'XPO:0101132', 'abnormal apoptotic cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(417779, 'HP:0006740', 'Transitional cell carcinoma of the bladder', 'XPO:0100481', 'abnormal anatomical line', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(417780, 'HP:0006740', 'Transitional cell carcinoma of the bladder', 'XPO:0100890', 'abnormal pharyngeal cavity', 0.43333333333333335, 4.970960464763942, 1.4676794159707953, 'HP:0011793', 'Neoplasm by anatomical site'),
(417781, 'HP:0006740', 'Transitional cell carcinoma of the bladder', 'XPO:0101377', 'abnormal manicotto glandulare', 0.41935483870967744, 4.970960464763942, 1.4438131194629262, 'HP:0011793', 'Neoplasm by anatomical site'),
(417782, 'HP:0006740', 'Transitional cell carcinoma of the bladder', 'XPO:0100486', 'abnormal oral evagination', 0.41935483870967744, 4.970960464763942, 1.4438131194629262, 'HP:0011793', 'Neoplasm by anatomical site'),
(417783, 'HP:0006740', 'Transitional cell carcinoma of the bladder', 'XPO:0101333', 'abnormal barrier epithelial cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(417784, 'HP:0006740', 'Transitional cell carcinoma of the bladder', 'XPO:0100462', 'abnormal anterior foregut', 0.40625, 4.970960464763942, 1.4210744839065794, 'HP:0011793', 'Neoplasm by anatomical site'),
(417785, 'HP:0006740', 'Transitional cell carcinoma of the bladder', 'XPO:0100477', 'abnormal pericyte', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(417786, 'HP:0006740', 'Transitional cell carcinoma of the bladder', 'XPO:0101297', 'abnormal barrier cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(417787, 'HP:0006740', 'Transitional cell carcinoma of the bladder', 'XPO:0100986', 'abnormal gut epithelium', 0.40625, 4.970960464763942, 1.4210744839065794, 'HP:0011793', 'Neoplasm by anatomical site'),
(417788, 'HP:0006740', 'Transitional cell carcinoma of the bladder', 'XPO:0100799', 'abnormal genital ridge', 0.41935483870967744, 5.4478002382576385, 1.5114765596055648, 'HP:0000119', 'Abnormality of the genitourinary system'),
(417789, 'HP:0006740', 'Transitional cell carcinoma of the bladder', 'XPO:0101101', 'abnormal posterior foregut', 0.40625, 4.970960464763942, 1.4210744839065794, 'HP:0011793', 'Neoplasm by anatomical site'),
(417790, 'HP:0006740', 'Transitional cell carcinoma of the bladder', 'XPO:0115473', 'abnormally delayed phase of Mullerian duct', 0.41935483870967744, 5.4478002382576385, 1.5114765596055648, 'HP:0000119', 'Abnormality of the genitourinary system'),
(417791, 'HP:0006740', 'Transitional cell carcinoma of the bladder', 'XPO:0101004', 'abnormal acid secreting cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(417792, 'HP:0006740', 'Transitional cell carcinoma of the bladder', 'XPO:0101237', 'abnormal mucus secreting cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(417793, 'HP:0006740', 'Transitional cell carcinoma of the bladder', 'XPO:0101535', 'abnormal absorptive cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(417794, 'HP:0006740', 'Transitional cell carcinoma of the bladder', 'XPO:0100549', 'abnormal mitotic cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(417795, 'HP:0006740', 'Transitional cell carcinoma of the bladder', 'XPO:0100715', 'abnormal ciliated cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(417796, 'HP:0006740', 'Transitional cell carcinoma of the bladder', 'XPO:0100006', 'abnormal anatomical structure', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(417797, 'HP:0006740', 'Transitional cell carcinoma of the bladder', 'XPO:0100337', 'abnormal zygote', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(417798, 'HP:0006740', 'Transitional cell carcinoma of the bladder', 'XPO:0142054', 'abnormal digestive tract', 0.43333333333333335, 4.970960464763942, 1.4676794159707953, 'HP:0011793', 'Neoplasm by anatomical site'),
(417799, 'HP:0006740', 'Transitional cell carcinoma of the bladder', 'XPO:0100026', 'abnormal germ cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(417800, 'HP:0006740', 'Transitional cell carcinoma of the bladder', 'XPO:0101326', 'abnormal cementoblast', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(417801, 'HP:0006740', 'Transitional cell carcinoma of the bladder', 'XPO:0101435', 'abnormal paracrine cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(417802, 'HP:0006740', 'Transitional cell carcinoma of the bladder', 'XPO:0100501', 'abnormal urogenital system', 0.5, 5.4478002382576385, 1.6504242239887355, 'HP:0000119', 'Abnormality of the genitourinary system'),
(417803, 'HP:0006740', 'Transitional cell carcinoma of the bladder', 'XPO:0100523', 'abnormal midgut', 0.41935483870967744, 4.970960464763942, 1.4438131194629262, 'HP:0011793', 'Neoplasm by anatomical site'),
(417804, 'HP:0006740', 'Transitional cell carcinoma of the bladder', 'XPO:0100081', 'abnormal anatomical entity in vitro', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(417805, 'HP:0006740', 'Transitional cell carcinoma of the bladder', 'XPO:0100156', 'abnormal foregut', 0.41935483870967744, 4.970960464763942, 1.4438131194629262, 'HP:0011793', 'Neoplasm by anatomical site'),
