(105023, 'HP:0030639', 'Congenital stationary night blindness with abnormal fundus', 'XPO:0130614', 'increased size of the retinal progenitor cell', 0.4056603773584906, 8.040873045973026, 1.8060630094548564, 'HP:0000479', 'Abnormal retinal morphology'),
(105024, 'HP:0030639', 'Congenital stationary night blindness with abnormal fundus', 'XPO:0129138', 'decreased size of the retinal progenitor cell', 0.4056603773584906, 8.040873045973026, 1.8060630094548564, 'HP:0000479', 'Abnormal retinal morphology'),
(105025, 'HP:0030639', 'Congenital stationary night blindness with abnormal fundus', 'XPO:0102946', 'abnormal retinal inner nuclear layer morphology', 0.4574468085106383, 8.040873045973026, 1.9178820903589395, 'HP:0000479', 'Abnormal retinal morphology'),
(105026, 'HP:0030639', 'Congenital stationary night blindness with abnormal fundus', 'XPO:0128100', 'decreased size of the inner limiting membrane', 0.4215686274509804, 8.040873045973026, 1.8411354685352277, 'HP:0000479', 'Abnormal retinal morphology'),
(105027, 'HP:0030639', 'Congenital stationary night blindness with abnormal fundus', 'XPO:0102476', 'abnormal lens transitional zone morphology', 0.40229885057471265, 6.887869297006056, 1.6646266551675757, 'HP:0012372', 'Abnormal eye morphology'),
(105028, 'HP:0030639', 'Congenital stationary night blindness with abnormal fundus', 'XPO:0141182', 'abnormally necrotic inner limiting membrane', 0.42574257425742573, 8.040873045973026, 1.850227550835222, 'HP:0000479', 'Abnormal retinal morphology'),
(105029, 'HP:0030639', 'Congenital stationary night blindness with abnormal fundus', 'XPO:0128787', 'decreased size of the peripheral retina', 0.4725274725274725, 8.040873045973026, 1.9492391893577128, 'HP:0000479', 'Abnormal retinal morphology'),
(105030, 'HP:0030639', 'Congenital stationary night blindness with abnormal fundus', 'XPO:0102996', 'abnormal optic fiber layer morphology', 0.4574468085106383, 8.040873045973026, 1.9178820903589395, 'HP:0000479', 'Abnormal retinal morphology'),
(105031, 'HP:0030639', 'Congenital stationary night blindness with abnormal fundus', 'XPO:0140240', 'abnormally necrotic eye photoreceptor cell', 0.42574257425742573, 8.040873045973026, 1.850227550835222, 'HP:0000479', 'Abnormal retinal morphology'),
(105032, 'HP:0030639', 'Congenital stationary night blindness with abnormal fundus', 'XPO:0141033', 'abnormally necrotic photoreceptor layer', 0.43, 8.040873045973026, 1.859455675666511, 'HP:0000479', 'Abnormal retinal morphology'),
(105033, 'HP:0030639', 'Congenital stationary night blindness with abnormal fundus', 'XPO:0128643', 'decreased size of the retinal layer', 0.5058823529411764, 8.040873045973026, 2.0168628550791743, 'HP:0000479', 'Abnormal retinal morphology'),
(105034, 'HP:0030639', 'Congenital stationary night blindness with abnormal fundus', 'XPO:0140948', 'abnormally necrotic retinal inner nuclear layer', 0.42574257425742573, 8.040873045973026, 1.850227550835222, 'HP:0000479', 'Abnormal retinal morphology'),
(105035, 'HP:0030639', 'Congenital stationary night blindness with abnormal fundus', 'XPO:0140346', 'abnormally necrotic retinal blood vessel', 0.41346153846153844, 8.040873045973026, 1.8233463028623837, 'HP:0000479', 'Abnormal retinal morphology'),
(105036, 'HP:0030639', 'Congenital stationary night blindness with abnormal fundus', 'XPO:0130845', 'increased size of the retinal outer plexiform layer', 0.4215686274509804, 8.040873045973026, 1.8411354685352277, 'HP:0000479', 'Abnormal retinal morphology'),
(105037, 'HP:0030639', 'Congenital stationary night blindness with abnormal fundus', 'XPO:0102239', 'abnormal retinal pigmented epithelium morphology', 0.4574468085106383, 8.040873045973026, 1.9178820903589395, 'HP:0000479', 'Abnormal retinal morphology'),
(105038, 'HP:0030639', 'Congenital stationary night blindness with abnormal fundus', 'XPO:0115423', 'abnormally incomplete structure of eye', 0.4268292682926829, 6.887869297006056, 1.714626551799759, 'HP:0012372', 'Abnormal eye morphology'),
(105039, 'HP:0030639', 'Congenital stationary night blindness with abnormal fundus', 'XPO:0102784', 'abnormal retinal progenitor cell region morphology', 0.5119047619047619, 8.040873045973026, 2.028832472656439, 'HP:0000479', 'Abnormal retinal morphology'),
(105040, 'HP:0030639', 'Congenital stationary night blindness with abnormal fundus', 'XPO:0102818', 'abnormal optic chiasm morphology', 0.44086021505376344, 7.796308075334707, 1.8539369068869231, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(105041, 'HP:0030639', 'Congenital stationary night blindness with abnormal fundus', 'XPO:0129810', 'increased size of the retinal progenitor cell region', 0.48314606741573035, 8.040873045973026, 1.9710190741722953, 'HP:0000479', 'Abnormal retinal morphology'),
(105042, 'HP:0030639', 'Congenital stationary night blindness with abnormal fundus', 'XPO:0130122', 'increased size of the retinal layer', 0.5058823529411764, 8.040873045973026, 2.0168628550791743, 'HP:0000479', 'Abnormal retinal morphology'),
(105043, 'HP:0030639', 'Congenital stationary night blindness with abnormal fundus', 'XPO:0128669', 'decreased size of the ciliary marginal zone', 0.4387755102040816, 8.040873045973026, 1.8783338822565765, 'HP:0000479', 'Abnormal retinal morphology'),
(105044, 'HP:0030639', 'Congenital stationary night blindness with abnormal fundus', 'XPO:0130761', 'increased size of the retinal inner plexiform layer', 0.4215686274509804, 8.040873045973026, 1.8411354685352277, 'HP:0000479', 'Abnormal retinal morphology'),
(105045, 'HP:0030639', 'Congenital stationary night blindness with abnormal fundus', 'XPO:0140192', 'abnormally necrotic retina', 0.5058823529411764, 8.040873045973026, 2.0168628550791743, 'HP:0000479', 'Abnormal retinal morphology'),
(105046, 'HP:0030639', 'Congenital stationary night blindness with abnormal fundus', 'XPO:0102882', 'abnormal retinal cone cell morphology', 0.43434343434343436, 8.040873045973026, 1.8688232698432123, 'HP:0000479', 'Abnormal retinal morphology'),
(105047, 'HP:0030639', 'Congenital stationary night blindness with abnormal fundus', 'XPO:0140218', 'abnormally necrotic sclera', 0.40229885057471265, 6.887869297006056, 1.6646266551675757, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(105048, 'HP:0030639', 'Congenital stationary night blindness with abnormal fundus', 'XPO:0102017', 'abnormal retinal neural layer morphology', 0.46236559139784944, 8.040873045973026, 1.9281657141584967, 'HP:0000479', 'Abnormal retinal morphology'),
(105049, 'HP:0030639', 'Congenital stationary night blindness with abnormal fundus', 'XPO:0140869', 'abnormally necrotic optic chiasm', 0.41836734693877553, 7.796308075334707, 1.8060234564908433, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(105050, 'HP:0030639', 'Congenital stationary night blindness with abnormal fundus', 'XPO:0128300', 'decreased size of the retina', 0.4942528735632184, 8.040873045973026, 1.9935457378573478, 'HP:0000479', 'Abnormal retinal morphology'),
(105051, 'HP:0030639', 'Congenital stationary night blindness with abnormal fundus', 'XPO:0102196', 'abnormal central retina morphology', 0.5375, 8.040873045973026, 2.0789346459690603, 'HP:0000479', 'Abnormal retinal morphology'),
(105052, 'HP:0030639', 'Congenital stationary night blindness with abnormal fundus', 'XPO:0140945', 'abnormally necrotic retinal ganglion cell layer', 0.42574257425742573, 8.040873045973026, 1.850227550835222, 'HP:0000479', 'Abnormal retinal morphology'),
(105053, 'HP:0030639', 'Congenital stationary night blindness with abnormal fundus', 'XPO:0128431', 'decreased size of the retinal inner nuclear layer', 0.4215686274509804, 8.040873045973026, 1.8411354685352277, 'HP:0000479', 'Abnormal retinal morphology'),
(105054, 'HP:0030639', 'Congenital stationary night blindness with abnormal fundus', 'XPO:0129955', 'increased size of the retinal stem cell region', 0.48314606741573035, 8.040873045973026, 1.9710190741722953, 'HP:0000479', 'Abnormal retinal morphology'),
(105055, 'HP:0030639', 'Congenital stationary night blindness with abnormal fundus', 'XPO:0140620', 'abnormally necrotic horizontal cell', 0.4174757281553398, 8.040873045973026, 1.8321761186829812, 'HP:0000479', 'Abnormal retinal morphology'),
(105056, 'HP:0030639', 'Congenital stationary night blindness with abnormal fundus', 'XPO:0128875', 'decreased size of the photoreceptor layer', 0.42574257425742573, 8.040873045973026, 1.850227550835222, 'HP:0000479', 'Abnormal retinal morphology'),
(105057, 'HP:0030639', 'Congenital stationary night blindness with abnormal fundus', 'XPO:0140491', 'abnormally necrotic retinal rod cell', 0.41346153846153844, 8.040873045973026, 1.8233463028623837, 'HP:0000479', 'Abnormal retinal morphology'),
(105058, 'HP:0030639', 'Congenital stationary night blindness with abnormal fundus', 'XPO:0140271', 'abnormally necrotic peripheral retina', 0.48314606741573035, 8.040873045973026, 1.9710190741722953, 'HP:0000479', 'Abnormal retinal morphology'),
(105059, 'HP:0030639', 'Congenital stationary night blindness with abnormal fundus', 'XPO:0102939', 'abnormal retinal ganglion cell layer morphology', 0.4574468085106383, 8.040873045973026, 1.9178820903589395, 'HP:0000479', 'Abnormal retinal morphology'),
(105060, 'HP:0030639', 'Congenital stationary night blindness with abnormal fundus', 'XPO:0102963', 'abnormal retinal outer nuclear layer morphology', 0.4574468085106383, 8.040873045973026, 1.9178820903589395, 'HP:0000479', 'Abnormal retinal morphology'),
(105061, 'HP:0030639', 'Congenital stationary night blindness with abnormal fundus', 'XPO:0128935', 'decreased size of the central retina', 0.5058823529411764, 8.040873045973026, 2.0168628550791743, 'HP:0000479', 'Abnormal retinal morphology'),
(105062, 'HP:0030639', 'Congenital stationary night blindness with abnormal fundus', 'XPO:0128330', 'decreased size of the retinal progenitor cell region', 0.48314606741573035, 8.040873045973026, 1.9710190741722953, 'HP:0000479', 'Abnormal retinal morphology'),
(105063, 'HP:0030639', 'Congenital stationary night blindness with abnormal fundus', 'XPO:0130125', 'increased size of the outer limiting membrane', 0.4215686274509804, 8.040873045973026, 1.8411354685352277, 'HP:0000479', 'Abnormal retinal morphology'),
(105064, 'HP:0030639', 'Congenital stationary night blindness with abnormal fundus', 'XPO:0130506', 'increased size of the Muller cell', 0.42574257425742573, 8.040873045973026, 1.850227550835222, 'HP:0000479', 'Abnormal retinal morphology'),
(105065, 'HP:0030639', 'Congenital stationary night blindness with abnormal fundus', 'XPO:0129741', 'increased size of the optic fiber layer', 0.4215686274509804, 8.040873045973026, 1.8411354685352277, 'HP:0000479', 'Abnormal retinal morphology'),
(105066, 'HP:0030639', 'Congenital stationary night blindness with abnormal fundus', 'XPO:0101861', 'abnormal photoreceptor layer morphology', 0.46236559139784944, 8.040873045973026, 1.9281657141584967, 'HP:0000479', 'Abnormal retinal morphology'),
(105067, 'HP:0030639', 'Congenital stationary night blindness with abnormal fundus', 'XPO:0140489', 'abnormally necrotic ciliary marginal zone', 0.4479166666666667, 8.040873045973026, 1.8977990019604511, 'HP:0000479', 'Abnormal retinal morphology'),
(105068, 'HP:0030639', 'Congenital stationary night blindness with abnormal fundus', 'XPO:0129780', 'increased size of the retina', 0.4942528735632184, 8.040873045973026, 1.9935457378573478, 'HP:0000479', 'Abnormal retinal morphology'),
(105069, 'HP:0030639', 'Congenital stationary night blindness with abnormal fundus', 'XPO:0129981', 'increased size of the retinal ganglion cell layer', 0.4215686274509804, 8.040873045973026, 1.8411354685352277, 'HP:0000479', 'Abnormal retinal morphology'),
(105070, 'HP:0030639', 'Congenital stationary night blindness with abnormal fundus', 'XPO:0130257', 'increased size of the retinal blood vessel', 0.4056603773584906, 8.040873045973026, 1.8060630094548564, 'HP:0000479', 'Abnormal retinal morphology'),
(105071, 'HP:0030639', 'Congenital stationary night blindness with abnormal fundus', 'XPO:0140391', 'abnormally necrotic central retina', 0.5180722891566265, 8.040873045973026, 2.0410177622316423, 'HP:0000479', 'Abnormal retinal morphology'),
(105072, 'HP:0030639', 'Congenital stationary night blindness with abnormal fundus', 'XPO:0130353', 'increased size of the photoreceptor layer', 0.42574257425742573, 8.040873045973026, 1.850227550835222, 'HP:0000479', 'Abnormal retinal morphology'),
(105073, 'HP:0030639', 'Congenital stationary night blindness with abnormal fundus', 'XPO:0133372', 'eye fused with olfactory epithelium', 0.4166666666666667, 6.887869297006056, 1.6940913612964297, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(105074, 'HP:0030639', 'Congenital stationary night blindness with abnormal fundus', 'XPO:0102117', 'abnormal retina morphology', 0.5375, 8.040873045973026, 2.0789346459690603, 'HP:0000479', 'Abnormal retinal morphology'),
(105075, 'HP:0030639', 'Congenital stationary night blindness with abnormal fundus', 'XPO:0140464', 'abnormally necrotic retinal pigmented epithelium', 0.4215686274509804, 8.040873045973026, 1.8411354685352277, 'HP:0000479', 'Abnormal retinal morphology'),
(105076, 'HP:0030639', 'Congenital stationary night blindness with abnormal fundus', 'XPO:0141323', 'edematous eye', 0.42168674698795183, 6.887869297006056, 1.7042661756699493, 'HP:0012372', 'Abnormal eye morphology'),
(105077, 'HP:0030639', 'Congenital stationary night blindness with abnormal fundus', 'XPO:0102232', 'abnormal eye photoreceptor cell morphology', 0.44329896907216493, 8.040873045973026, 1.8879911895239345, 'HP:0000479', 'Abnormal retinal morphology'),
(105078, 'HP:0030639', 'Congenital stationary night blindness with abnormal fundus', 'XPO:0102815', 'abnormal retinal ganglion cell morphology', 0.43, 8.040873045973026, 1.859455675666511, 'HP:0000479', 'Abnormal retinal morphology'),
(105079, 'HP:0030639', 'Congenital stationary night blindness with abnormal fundus', 'XPO:0128779', 'decreased size of the retinal blood vessel', 0.4056603773584906, 8.040873045973026, 1.8060630094548564, 'HP:0000479', 'Abnormal retinal morphology'),
(105080, 'HP:0030639', 'Congenital stationary night blindness with abnormal fundus', 'XPO:0141337', 'increased pigmentation in the eye', 0.4166666666666667, 6.887869297006056, 1.6940913612964297, 'HP:0012372', 'Abnormal eye morphology'),
(105081, 'HP:0030639', 'Congenital stationary night blindness with abnormal fundus', 'XPO:0129038', 'decreased size of the retinal outer nuclear layer', 0.4215686274509804, 8.040873045973026, 1.8411354685352277, 'HP:0000479', 'Abnormal retinal morphology'),
(105082, 'HP:0030639', 'Congenital stationary night blindness with abnormal fundus', 'XPO:0130148', 'increased size of the ciliary marginal zone', 0.4387755102040816, 8.040873045973026, 1.8783338822565765, 'HP:0000479', 'Abnormal retinal morphology'),
(105083, 'HP:0030639', 'Congenital stationary night blindness with abnormal fundus', 'XPO:0101961', 'abnormal retinal blood vessel morphology', 0.44329896907216493, 8.040873045973026, 1.8879911895239345, 'HP:0000479', 'Abnormal retinal morphology'),
(105084, 'HP:0030639', 'Congenital stationary night blindness with abnormal fundus', 'XPO:0129775', 'increased size of the retinal neural layer', 0.4215686274509804, 8.040873045973026, 1.8411354685352277, 'HP:0000479', 'Abnormal retinal morphology'),
(105085, 'HP:0030639', 'Congenital stationary night blindness with abnormal fundus', 'XPO:0129371', 'decreased size of the retinal outer plexiform layer', 0.4215686274509804, 8.040873045973026, 1.8411354685352277, 'HP:0000479', 'Abnormal retinal morphology'),
(105086, 'HP:0030639', 'Congenital stationary night blindness with abnormal fundus', 'XPO:0141638', 'neoplastic eye', 0.4166666666666667, 6.887869297006056, 1.6940913612964297, 'HP:0012372', 'Abnormal eye morphology'),
(105087, 'HP:0030639', 'Congenital stationary night blindness with abnormal fundus', 'XPO:0133371', 'eye fused with olfactory pit', 0.4166666666666667, 6.887869297006056, 1.6940913612964297, 'HP:0012372', 'Abnormal eye morphology'),
(105088, 'HP:0030639', 'Congenital stationary night blindness with abnormal fundus', 'XPO:0102162', 'abnormal ciliary marginal zone morphology', 0.48863636363636365, 8.040873045973026, 1.982186410418029, 'HP:0000479', 'Abnormal retinal morphology'),
(105089, 'HP:0030639', 'Congenital stationary night blindness with abnormal fundus', 'XPO:0103086', 'abnormal amacrine cell morphology', 0.42574257425742573, 8.040873045973026, 1.850227550835222, 'HP:0000479', 'Abnormal retinal morphology'),
(105090, 'HP:0030639', 'Congenital stationary night blindness with abnormal fundus', 'XPO:0130362', 'increased size of the retinal pigmented epithelium', 0.4174757281553398, 8.040873045973026, 1.8321761186829812, 'HP:0000479', 'Abnormal retinal morphology'),
(105091, 'HP:0030639', 'Congenital stationary night blindness with abnormal fundus', 'XPO:0100371', 'abnormal hyaloid blood vessel', 0.4025974025974026, 6.887869297006056, 1.6652442128423794, 'HP:0012372', 'Abnormal eye morphology'),
(105092, 'HP:0030639', 'Congenital stationary night blindness with abnormal fundus', 'XPO:0140808', 'abnormally necrotic retinal cone cell', 0.41346153846153844, 8.040873045973026, 1.8233463028623837, 'HP:0000479', 'Abnormal retinal morphology'),
(105093, 'HP:0030639', 'Congenital stationary night blindness with abnormal fundus', 'XPO:0128475', 'decreased size of the retinal stem cell region', 0.48314606741573035, 8.040873045973026, 1.9710190741722953, 'HP:0000479', 'Abnormal retinal morphology'),
(105094, 'HP:0030639', 'Congenital stationary night blindness with abnormal fundus', 'XPO:0130189', 'increased size of the optic chiasm', 0.4019607843137255, 7.796308075334707, 1.7702570741880883, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(105095, 'HP:0030639', 'Congenital stationary night blindness with abnormal fundus', 'XPO:0140487', 'abnormally necrotic retinal layer', 0.5119047619047619, 8.040873045973026, 2.028832472656439, 'HP:0000479', 'Abnormal retinal morphology'),
(105096, 'HP:0030639', 'Congenital stationary night blindness with abnormal fundus', 'XPO:0128261', 'decreased size of the optic fiber layer', 0.4215686274509804, 8.040873045973026, 1.8411354685352277, 'HP:0000479', 'Abnormal retinal morphology'),
(105097, 'HP:0030639', 'Congenital stationary night blindness with abnormal fundus', 'XPO:0102663', 'abnormal retinal progenitor cell morphology', 0.46236559139784944, 8.040873045973026, 1.9281657141584967, 'HP:0000479', 'Abnormal retinal morphology'),
(105098, 'HP:0030639', 'Congenital stationary night blindness with abnormal fundus', 'XPO:0141343', 'decreased pigmentation in the eye', 0.4166666666666667, 6.887869297006056, 1.6940913612964297, 'HP:0012372', 'Abnormal eye morphology'),
(105099, 'HP:0030639', 'Congenital stationary night blindness with abnormal fundus', 'XPO:0103184', 'abnormal inner limiting membrane morphology', 0.4574468085106383, 8.040873045973026, 1.9178820903589395, 'HP:0000479', 'Abnormal retinal morphology'),
(105100, 'HP:0030639', 'Congenital stationary night blindness with abnormal fundus', 'XPO:0139912', 'abnormally necrotic optic fiber layer', 0.42574257425742573, 8.040873045973026, 1.850227550835222, 'HP:0000479', 'Abnormal retinal morphology'),
(105101, 'HP:0030639', 'Congenital stationary night blindness with abnormal fundus', 'XPO:0141333', 'increased pigmentation in the retinal pigmented epithelium', 0.44329896907216493, 8.040873045973026, 1.8879911895239345, 'HP:0000479', 'Abnormal retinal morphology'),
(105102, 'HP:0030639', 'Congenital stationary night blindness with abnormal fundus', 'XPO:0140081', 'abnormally necrotic amacrine cell', 0.40186915887850466, 8.040873045973026, 1.797603651429875, 'HP:0000479', 'Abnormal retinal morphology'),
(105103, 'HP:0030639', 'Congenital stationary night blindness with abnormal fundus', 'XPO:0101817', 'abnormal eye morphology', 0.43209876543209874, 6.887869297006056, 1.7251781994025936, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(105104, 'HP:0030639', 'Congenital stationary night blindness with abnormal fundus', 'XPO:0102441', 'abnormal retinal inner plexiform layer morphology', 0.4574468085106383, 8.040873045973026, 1.9178820903589395, 'HP:0000479', 'Abnormal retinal morphology'),
(105105, 'HP:0030639', 'Congenital stationary night blindness with abnormal fundus', 'XPO:0140671', 'abnormally necrotic retinal ganglion cell', 0.4095238095238095, 8.040873045973026, 1.8146429295275122, 'HP:0000479', 'Abnormal retinal morphology'),
(105106, 'HP:0030639', 'Congenital stationary night blindness with abnormal fundus', 'XPO:0100329', 'abnormal retinal blood vessel', 0.5443037974683544, 8.040873045973026, 2.0920510830006163, 'HP:0000479', 'Abnormal retinal morphology'),
(105107, 'HP:0030639', 'Congenital stationary night blindness with abnormal fundus', 'XPO:0128710', 'decreased size of the optic chiasm', 0.4019607843137255, 7.796308075334707, 1.7702570741880883, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(105108, 'HP:0030639', 'Congenital stationary night blindness with abnormal fundus', 'XPO:0141138', 'abnormally necrotic retinal inner plexiform layer', 0.42574257425742573, 8.040873045973026, 1.850227550835222, 'HP:0000479', 'Abnormal retinal morphology'),
(105109, 'HP:0030639', 'Congenital stationary night blindness with abnormal fundus', 'XPO:0130265', 'increased size of the peripheral retina', 0.4725274725274725, 8.040873045973026, 1.9492391893577128, 'HP:0000479', 'Abnormal retinal morphology'),
(105110, 'HP:0030639', 'Congenital stationary night blindness with abnormal fundus', 'XPO:0129029', 'decreased size of the Muller cell', 0.42574257425742573, 8.040873045973026, 1.850227550835222, 'HP:0000479', 'Abnormal retinal morphology'),
(105111, 'HP:0030639', 'Congenital stationary night blindness with abnormal fundus', 'XPO:0140553', 'abnormally necrotic retinal stem cell region', 0.4942528735632184, 8.040873045973026, 1.9935457378573478, 'HP:0000479', 'Abnormal retinal morphology'),
(105112, 'HP:0030639', 'Congenital stationary night blindness with abnormal fundus', 'XPO:0128884', 'decreased size of the retinal pigmented epithelium', 0.4174757281553398, 8.040873045973026, 1.8321761186829812, 'HP:0000479', 'Abnormal retinal morphology'),
(105113, 'HP:0030639', 'Congenital stationary night blindness with abnormal fundus', 'XPO:0130413', 'increased size of the central retina', 0.5058823529411764, 8.040873045973026, 2.0168628550791743, 'HP:0000479', 'Abnormal retinal morphology'),
(105114, 'HP:0030639', 'Congenital stationary night blindness with abnormal fundus', 'XPO:0102550', 'abnormal lens morphology', 0.4117647058823529, 6.887869297006056, 1.6840966347682629, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(105115, 'HP:0030639', 'Congenital stationary night blindness with abnormal fundus', 'XPO:0125909', 'absent retinal blood vessel', 0.4574468085106383, 8.040873045973026, 1.9178820903589395, 'HP:0000479', 'Abnormal retinal morphology'),
(105116, 'HP:0030639', 'Congenital stationary night blindness with abnormal fundus', 'XPO:0102513', 'abnormal sclera morphology', 0.4268292682926829, 6.887869297006056, 1.714626551799759, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(105117, 'HP:0030639', 'Congenital stationary night blindness with abnormal fundus', 'XPO:0102581', 'abnormal outer limiting membrane morphology', 0.4574468085106383, 8.040873045973026, 1.9178820903589395, 'HP:0000479', 'Abnormal retinal morphology'),
(105118, 'HP:0030639', 'Congenital stationary night blindness with abnormal fundus', 'XPO:0129911', 'increased size of the retinal inner nuclear layer', 0.4215686274509804, 8.040873045973026, 1.8411354685352277, 'HP:0000479', 'Abnormal retinal morphology'),
(105119, 'HP:0030639', 'Congenital stationary night blindness with abnormal fundus', 'XPO:0133369', 'eye fused with brain', 0.4166666666666667, 6.887869297006056, 1.6940913612964297, 'HP:0012372', 'Abnormal eye morphology'),
(105120, 'HP:0030639', 'Congenital stationary night blindness with abnormal fundus', 'XPO:0140797', 'abnormally necrotic bipolar neuron', 0.40186915887850466, 8.040873045973026, 1.797603651429875, 'HP:0000479', 'Abnormal retinal morphology'),
(105121, 'HP:0030639', 'Congenital stationary night blindness with abnormal fundus', 'XPO:0141014', 'abnormally necrotic retinal outer plexiform layer', 0.42574257425742573, 8.040873045973026, 1.850227550835222, 'HP:0000479', 'Abnormal retinal morphology'),
(105122, 'HP:0010577', 'Absent epiphyses', 'XPO:0102567', 'abnormal skeleton morphology', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(105123, 'HP:0010577', 'Absent epiphyses', 'XPO:0125893', 'absent flexural organ', 0.42857142857142855, 8.306662838606666, 1.886795791653897, 'UPHENO:0026023', 'absent anatomical entity in the skeletal system'),
(105124, 'HP:0010577', 'Absent epiphyses', 'XPO:0125800', 'absent joint', 0.40384615384615385, 8.306662838606666, 1.8315604927678684, 'UPHENO:0026023', 'absent anatomical entity in the skeletal system'),
(105125, 'HP:0010577', 'Absent epiphyses', 'XPO:0141689', 'absent anterior notochord', 0.42857142857142855, 8.306662838606666, 1.886795791653897, 'UPHENO:0026023', 'absent anatomical entity in the skeletal system'),
(105126, 'HP:0010577', 'Absent epiphyses', 'XPO:0125380', 'absent skeletal system', 0.425531914893617, 5.877776558317607, 1.5815124135389216, 'UPHENO:0026506', 'absent anatomical entity in the multicellular organism'),
(105127, 'HP:0010577', 'Absent epiphyses', 'XPO:0141719', 'abnormal anterior notochord morphology', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(105128, 'HP:0010577', 'Absent epiphyses', 'XPO:0125930', 'absent articular system', 0.4375, 8.306662838606666, 1.9063486018801536, 'UPHENO:0026023', 'absent anatomical entity in the skeletal system'),
(105129, 'HP:0010577', 'Absent epiphyses', 'XPO:0125036', 'absent axial skeleton', 0.40384615384615385, 8.306662838606666, 1.8315604927678684, 'UPHENO:0026023', 'absent anatomical entity in the skeletal system'),
(105130, 'HP:0010577', 'Absent epiphyses', 'XPO:0141723', 'abnormal posterior notochord morphology', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(105131, 'HP:0010577', 'Absent epiphyses', 'XPO:0125625', 'absent endoskeleton', 0.40384615384615385, 8.306662838606666, 1.8315604927678684, 'UPHENO:0026023', 'absent anatomical entity in the skeletal system'),
(105132, 'HP:0010577', 'Absent epiphyses', 'XPO:0125008', 'absent perichondrium', 0.42, 8.306662838606666, 1.8678325385897956, 'UPHENO:0026023', 'absent anatomical entity in the skeletal system'),
(105133, 'HP:0010577', 'Absent epiphyses', 'XPO:0102806', 'abnormal articular system morphology', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(105134, 'HP:0010577', 'Absent epiphyses', 'XPO:0102097', 'abnormal skeletal system morphology', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(105135, 'HP:0010577', 'Absent epiphyses', 'XPO:0124813', 'absent skeletal subdivision', 0.42, 8.306662838606666, 1.8678325385897956, 'UPHENO:0026023', 'absent anatomical entity in the skeletal system'),
(105136, 'HP:0010577', 'Absent epiphyses', 'XPO:0125226', 'absent appendicular skeleton', 0.40384615384615385, 8.306662838606666, 1.8315604927678684, 'UPHENO:0026023', 'absent anatomical entity in the skeletal system'),
(105137, 'HP:0010577', 'Absent epiphyses', 'XPO:0103303', 'absent notochord', 0.42857142857142855, 8.306662838606666, 1.886795791653897, 'UPHENO:0026023', 'absent anatomical entity in the skeletal system'),
(105138, 'HP:0010577', 'Absent epiphyses', 'XPO:0124812', 'absent dermal skeleton', 0.40384615384615385, 8.306662838606666, 1.8315604927678684, 'UPHENO:0026023', 'absent anatomical entity in the skeletal system'),
(105139, 'HP:0010577', 'Absent epiphyses', 'XPO:0125215', 'absent skeleton', 0.42857142857142855, 8.306662838606666, 1.886795791653897, 'UPHENO:0026023', 'absent anatomical entity in the skeletal system'),
(105140, 'HP:0010577', 'Absent epiphyses', 'XPO:0126189', 'absent notochordal sheath', 0.42857142857142855, 8.306662838606666, 1.886795791653897, 'UPHENO:0026023', 'absent anatomical entity in the skeletal system'),
(105141, 'HP:0010577', 'Absent epiphyses', 'XPO:0102217', 'abnormal elastica externa morphology', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(105142, 'HP:0010577', 'Absent epiphyses', 'XPO:0141693', 'absent posterior notochord', 0.42857142857142855, 8.306662838606666, 1.886795791653897, 'UPHENO:0026023', 'absent anatomical entity in the skeletal system'),
(105143, 'HP:0010577', 'Absent epiphyses', 'XPO:0125260', 'absent vertebral column', 0.43333333333333335, 8.306662838606666, 1.8972490339250552, 'UPHENO:0026023', 'absent anatomical entity in the skeletal system'),
(105144, 'HP:0010577', 'Absent epiphyses', 'XPO:0102054', 'abnormal notochord morphology', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(105145, 'HP:0010577', 'Absent epiphyses', 'XPO:0101982', 'abnormal appendicular skeleton morphology', 0.4230769230769231, 5.732269579595698, 1.557302467725135, 'HP:0011844', 'Abnormal appendicular skeleton morphology'),
(105146, 'HP:0010577', 'Absent epiphyses', 'XPO:0125099', 'absent elastica externa', 0.45652173913043476, 8.306662838606666, 1.9473500367039482, 'UPHENO:0026023', 'absent anatomical entity in the skeletal system'),
(105147, 'HP:0010577', 'Absent epiphyses', 'XPO:0107372', 'abnormal flexural organ morphology', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(105148, 'HP:0010577', 'Absent epiphyses', 'XPO:0102272', 'abnormal notochordal sheath morphology', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(105149, 'HP:0002414', 'Spina bifida', 'XPO:0131746', 'abnormal neural tube closure', 0.5333333333333333, 12.484129389061598, 2.580349267218074, 'UPHENO:0051077', 'abnormal neural tube closure'),
(105150, 'HP:0011253', 'Type I cryptotia', 'XPO:0100850', 'abnormal auditory tube', 0.41509433962264153, 7.26295268789559, 1.7363209811819096, 'UPHENO:0076730', 'abnormal ear morphology'),
(105151, 'HP:0011253', 'Type I cryptotia', 'XPO:0102538', 'abnormal lateral nasal prominence morphology', 0.42857142857142855, 4.5318002188002176, 1.3936283915633758, 'UPHENO:0087907', 'abnormal head morphology'),
(105152, 'HP:0011253', 'Type I cryptotia', 'XPO:0103739', 'increased size of the pharyngeal region', 0.42, 4.5318002188002176, 1.3796217205799897, 'UPHENO:0087907', 'abnormal head morphology'),
(105153, 'HP:0011253', 'Type I cryptotia', 'XPO:0141835', 'edematous head', 0.4375, 4.5318002188002176, 1.4080705222839853, 'UPHENO:0087907', 'abnormal head morphology'),
(105154, 'HP:0011253', 'Type I cryptotia', 'XPO:0141298', 'abnormal intercanthal region morphology', 0.4375, 4.5318002188002176, 1.4080705222839853, 'UPHENO:0087907', 'abnormal head morphology'),
(105155, 'HP:0011253', 'Type I cryptotia', 'XPO:0141631', 'neoplastic auditory apparatus', 0.4098360655737705, 7.26295268789559, 1.7252883683765938, 'UPHENO:0076730', 'abnormal ear morphology'),
(105156, 'HP:0011253', 'Type I cryptotia', 'XPO:0102259', 'abnormal pharyngeal region morphology', 0.4666666666666667, 4.5318002188002176, 1.4542489821577214, 'UPHENO:0087907', 'abnormal head morphology'),
(105157, 'HP:0011253', 'Type I cryptotia', 'XPO:0101634', 'abnormal head morphology', 0.45652173913043476, 4.5318002188002176, 1.4383550734357495, 'UPHENO:0087907', 'abnormal head morphology'),
(105158, 'HP:0011253', 'Type I cryptotia', 'XPO:0102482', 'abnormal auditory tube morphology', 0.4098360655737705, 7.26295268789559, 1.7252883683765938, 'UPHENO:0076730', 'abnormal ear morphology'),
(105159, 'HP:0011253', 'Type I cryptotia', 'XPO:0142059', 'abnormal nasal region morphology', 0.44680851063829785, 4.5318002188002176, 1.422971154406314, 'UPHENO:0087907', 'abnormal head morphology'),
(105160, 'HP:0011253', 'Type I cryptotia', 'XPO:0141839', 'edematous pharyngeal region', 0.44680851063829785, 4.5318002188002176, 1.422971154406314, 'UPHENO:0087907', 'abnormal head morphology'),
(105161, 'HP:0011253', 'Type I cryptotia', 'XPO:0140223', 'abnormally necrotic head region', 0.4117647058823529, 4.5318002188002176, 1.3660290568695288, 'UPHENO:0087907', 'abnormal head morphology'),
(105162, 'HP:0011253', 'Type I cryptotia', 'XPO:0100536', 'abnormal inner ear', 0.4074074074074074, 7.26295268789559, 1.7201688070355778, 'UPHENO:0076730', 'abnormal ear morphology'),
(105163, 'HP:0011253', 'Type I cryptotia', 'XPO:0103358', 'decreased size of the pharyngeal region', 0.42, 4.5318002188002176, 1.3796217205799897, 'UPHENO:0087907', 'abnormal head morphology'),
(105164, 'HP:0011253', 'Type I cryptotia', 'XPO:0115526', 'abnormally incomplete structure of head', 0.44680851063829785, 4.5318002188002176, 1.422971154406314, 'UPHENO:0087907', 'abnormal head morphology'),
(105165, 'HP:0011253', 'Type I cryptotia', 'XPO:0140335', 'abnormally necrotic pharyngeal region', 0.4375, 4.5318002188002176, 1.4080705222839853, 'UPHENO:0087907', 'abnormal head morphology'),
(105166, 'HP:0011253', 'Type I cryptotia', 'XPO:0103101', 'abnormal medial nasal prominence morphology', 0.42857142857142855, 4.5318002188002176, 1.3936283915633758, 'UPHENO:0087907', 'abnormal head morphology'),
(105167, 'HP:0011253', 'Type I cryptotia', 'XPO:0141339', 'decreased pigmentation in the head', 0.42857142857142855, 4.5318002188002176, 1.3936283915633758, 'UPHENO:0087907', 'abnormal head morphology'),
(105168, 'HP:0011253', 'Type I cryptotia', 'XPO:0126939', 'abnormally localised auditory apparatus', 0.532258064516129, 10.484129389061598, 2.3622579064866294, 'UPHENO:0005986', 'abnormal shape of external ear'),
(105169, 'HP:0011253', 'Type I cryptotia', 'XPO:0139715', 'abnormally necrotic head', 0.4117647058823529, 4.5318002188002176, 1.3660290568695288, 'UPHENO:0087907', 'abnormal head morphology'),
(105170, 'HP:0011253', 'Type I cryptotia', 'XPO:0102804', 'abnormal pharyngeal pouch morphology', 0.42857142857142855, 4.5318002188002176, 1.3936283915633758, 'UPHENO:0087907', 'abnormal head morphology'),
(105171, 'HP:0011253', 'Type I cryptotia', 'XPO:0102572', 'abnormal hatching gland primordium morphology', 0.4117647058823529, 4.5318002188002176, 1.3660290568695288, 'UPHENO:0087907', 'abnormal head morphology'),
(105172, 'HP:0011253', 'Type I cryptotia', 'XPO:0140914', 'abnormally necrotic intercanthal region', 0.4117647058823529, 4.5318002188002176, 1.3660290568695288, 'UPHENO:0087907', 'abnormal head morphology'),
(105173, 'HP:0011253', 'Type I cryptotia', 'XPO:0101005', 'abnormal middle ear', 0.4074074074074074, 7.26295268789559, 1.7201688070355778, 'UPHENO:0076730', 'abnormal ear morphology'),
(105174, 'HP:0011253', 'Type I cryptotia', 'XPO:0102224', 'abnormal auditory apparatus morphology', 0.43103448275862066, 7.26295268789559, 1.769345374743837, 'UPHENO:0076730', 'abnormal ear morphology'),
(105175, 'HP:0011253', 'Type I cryptotia', 'XPO:0103707', 'increased pigmentation in the head', 0.42857142857142855, 4.5318002188002176, 1.3936283915633758, 'UPHENO:0087907', 'abnormal head morphology'),
(105176, 'HP:0011253', 'Type I cryptotia', 'XPO:0102082', 'abnormal circumpharyngeal ridge morphology', 0.42, 4.5318002188002176, 1.3796217205799897, 'UPHENO:0087907', 'abnormal head morphology'),
(105177, 'HP:0011253', 'Type I cryptotia', 'XPO:0102734', 'abnormal craniofacial region morphology', 0.42857142857142855, 4.5318002188002176, 1.3936283915633758, 'UPHENO:0087907', 'abnormal head morphology'),
(105178, 'HP:0004286', 'Patchy sclerosis of hand bones', 'XPO:0139774', 'abnormally necrotic elastica externa', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(105179, 'HP:0004286', 'Patchy sclerosis of hand bones', 'XPO:0102806', 'abnormal articular system morphology', 0.46511627906976744, 4.638757693672553, 1.4688640910537754, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(105180, 'HP:0004286', 'Patchy sclerosis of hand bones', 'XPO:0100584', 'abnormal vertebral column', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(105181, 'HP:0004286', 'Patchy sclerosis of hand bones', 'XPO:0102567', 'abnormal skeleton morphology', 0.45454545454545453, 4.638757693672553, 1.452076521536181, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(105182, 'HP:0004286', 'Patchy sclerosis of hand bones', 'XPO:0141719', 'abnormal anterior notochord morphology', 0.45454545454545453, 4.638757693672553, 1.452076521536181, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(105183, 'HP:0004286', 'Patchy sclerosis of hand bones', 'XPO:0140432', 'abnormally necrotic skeleton', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(105184, 'HP:0004286', 'Patchy sclerosis of hand bones', 'XPO:0101957', 'abnormal axial skeleton morphology', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(105185, 'HP:0004286', 'Patchy sclerosis of hand bones', 'XPO:0140559', 'abnormally necrotic articular system', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(105186, 'HP:0004286', 'Patchy sclerosis of hand bones', 'XPO:0102130', 'abnormal endoskeleton morphology', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(105187, 'HP:0004286', 'Patchy sclerosis of hand bones', 'XPO:0128352', 'decreased size of the skeletal system', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(105188, 'HP:0004286', 'Patchy sclerosis of hand bones', 'XPO:0102144', 'abnormal cranial skeleton morphology', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(105189, 'HP:0004286', 'Patchy sclerosis of hand bones', 'XPO:0102542', 'abnormal vacuolated notochordal tissue morphology', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(105190, 'HP:0004286', 'Patchy sclerosis of hand bones', 'XPO:0102054', 'abnormal notochord morphology', 0.45454545454545453, 4.638757693672553, 1.452076521536181, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(105191, 'HP:0004286', 'Patchy sclerosis of hand bones', 'XPO:0130368', 'increased size of the elastica externa', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(105192, 'HP:0004286', 'Patchy sclerosis of hand bones', 'XPO:0140019', 'abnormally necrotic skeletal system', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(105193, 'HP:0004286', 'Patchy sclerosis of hand bones', 'XPO:0102605', 'abnormal dermal skeleton morphology', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(105194, 'HP:0004286', 'Patchy sclerosis of hand bones', 'XPO:0102514', 'abnormal perichondrial cell morphology', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(105195, 'HP:0004286', 'Patchy sclerosis of hand bones', 'XPO:0140350', 'abnormally necrotic notochordal sheath', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(105196, 'HP:0004286', 'Patchy sclerosis of hand bones', 'XPO:0101982', 'abnormal appendicular skeleton morphology', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(105197, 'HP:0004286', 'Patchy sclerosis of hand bones', 'XPO:0141723', 'abnormal posterior notochord morphology', 0.45454545454545453, 4.638757693672553, 1.452076521536181, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(105198, 'HP:0004286', 'Patchy sclerosis of hand bones', 'XPO:0141699', 'abnormally necrotic anterior notochord', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(105199, 'HP:0004286', 'Patchy sclerosis of hand bones', 'XPO:0101860', 'abnormal skeletal subdivision morphology', 0.4444444444444444, 4.638757693672553, 1.4358516936218344, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(105200, 'HP:0004286', 'Patchy sclerosis of hand bones', 'XPO:0141703', 'abnormally necrotic posterior notochord', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(105201, 'HP:0004286', 'Patchy sclerosis of hand bones', 'XPO:0102010', 'abnormal perichondrium morphology', 0.4444444444444444, 4.638757693672553, 1.4358516936218344, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(105202, 'HP:0004286', 'Patchy sclerosis of hand bones', 'XPO:0102980', 'abnormal perichordal tissue morphology', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(105203, 'HP:0004286', 'Patchy sclerosis of hand bones', 'XPO:0102272', 'abnormal notochordal sheath morphology', 0.45454545454545453, 4.638757693672553, 1.452076521536181, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(105204, 'HP:0004286', 'Patchy sclerosis of hand bones', 'XPO:0129832', 'increased size of the skeletal system', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(105205, 'HP:0004286', 'Patchy sclerosis of hand bones', 'XPO:0102217', 'abnormal elastica externa morphology', 0.47619047619047616, 4.638757693672553, 1.4862477031377266, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(105206, 'HP:0004286', 'Patchy sclerosis of hand bones', 'XPO:0140683', 'abnormally necrotic flexural organ', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(105207, 'HP:0004286', 'Patchy sclerosis of hand bones', 'XPO:0107372', 'abnormal flexural organ morphology', 0.45454545454545453, 4.638757693672553, 1.452076521536181, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(105208, 'HP:0004286', 'Patchy sclerosis of hand bones', 'XPO:0102097', 'abnormal skeletal system morphology', 0.47619047619047616, 4.638757693672553, 1.4862477031377266, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(105209, 'HP:0004286', 'Patchy sclerosis of hand bones', 'XPO:0128890', 'decreased size of the elastica externa', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(105210, 'HP:5201010', 'Microform cleft of the upper lip', 'XPO:0129152', 'decreased size of the oral cavity', 0.47297297297297297, 7.884497199543557, 1.9311017790021312, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(105211, 'HP:5201010', 'Microform cleft of the upper lip', 'XPO:0103352', 'decreased size of the mouth', 0.44871794871794873, 7.884497199543557, 1.880934717115827, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(105212, 'HP:5201010', 'Microform cleft of the upper lip', 'XPO:0103096', 'abnormal oral cavity morphology', 0.5072463768115942, 7.884497199543557, 1.99984565340669, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(105213, 'HP:5201010', 'Microform cleft of the upper lip', 'XPO:0101567', 'abnormal tongue', 0.5079365079365079, 7.884497199543557, 2.0012056302067838, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(105214, 'HP:5201010', 'Microform cleft of the upper lip', 'XPO:0103735', 'increased size of the mouth', 0.44871794871794873, 7.884497199543557, 1.880934717115827, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(105215, 'HP:5201010', 'Microform cleft of the upper lip', 'XPO:0128105', 'decreased size of the tongue', 0.4268292682926829, 7.884497199543557, 1.8344847152639032, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(105216, 'HP:5201010', 'Microform cleft of the upper lip', 'XPO:0140639', 'abnormally necrotic upper jaw', 0.4090909090909091, 8.81758714901448, 1.8992616309446815, 'UPHENO:0087585', 'abnormal midface morphology'),
(105217, 'HP:5201010', 'Microform cleft of the upper lip', 'XPO:0101659', 'abnormal lower jaw morphology', 0.40963855421686746, 7.312692920701687, 1.7307688914087174, 'UPHENO:0076800', 'abnormal mouth morphology'),
(105218, 'HP:5201010', 'Microform cleft of the upper lip', 'XPO:0127750', 'abnormally localised tongue', 0.4520547945205479, 7.884497199543557, 1.8879154539961525, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(105219, 'HP:5201010', 'Microform cleft of the upper lip', 'XPO:0140626', 'abnormally necrotic tongue', 0.47297297297297297, 7.884497199543557, 1.9311017790021312, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(105220, 'HP:5201010', 'Microform cleft of the upper lip', 'XPO:0126089', 'absent tongue', 0.44, 7.884497199543557, 1.8625731577039237, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(105221, 'HP:5201010', 'Microform cleft of the upper lip', 'XPO:0102960', 'abnormal oral epithelium morphology', 0.4230769230769231, 7.312692920701687, 1.7589291117884391, 'UPHENO:0076800', 'abnormal mouth morphology'),
(105222, 'HP:5201010', 'Microform cleft of the upper lip', 'XPO:0129585', 'increased size of the tongue', 0.40229885057471265, 7.884497199543557, 1.7809896576723612, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(105223, 'HP:5201010', 'Microform cleft of the upper lip', 'XPO:0103199', 'abnormal tongue morphology', 0.5072463768115942, 7.884497199543557, 1.99984565340669, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(105224, 'HP:5201010', 'Microform cleft of the upper lip', 'XPO:0131611', 'increased size of the roof of mouth', 0.4177215189873418, 7.312692920701687, 1.7477611949930372, 'UPHENO:0076800', 'abnormal mouth morphology'),
(105225, 'HP:5201010', 'Microform cleft of the upper lip', 'XPO:0140789', 'abnormally necrotic roof of mouth', 0.42857142857142855, 7.312692920701687, 1.7703138850862843, 'UPHENO:0076800', 'abnormal mouth morphology'),
(105226, 'HP:5201010', 'Microform cleft of the upper lip', 'XPO:0103138', 'abnormal upper jaw morphology', 0.43373493975903615, 8.81758714901448, 1.9556317728288848, 'UPHENO:0087585', 'abnormal midface morphology'),
(105227, 'HP:5201010', 'Microform cleft of the upper lip', 'XPO:0131573', 'decreased size of the roof of mouth', 0.4177215189873418, 7.312692920701687, 1.7477611949930372, 'UPHENO:0076800', 'abnormal mouth morphology'),
(105228, 'HP:5201010', 'Microform cleft of the upper lip', 'XPO:0115558', 'abnormally incomplete structure of mouth', 0.4714285714285714, 7.312692920701687, 1.856720866716972, 'UPHENO:0076800', 'abnormal mouth morphology'),
(105229, 'HP:5201010', 'Microform cleft of the upper lip', 'XPO:0115393', 'abnormally decreased volume of oral cavity', 0.4605263157894737, 7.884497199543557, 1.9055231426456665, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(105230, 'HP:5201010', 'Microform cleft of the upper lip', 'XPO:0141830', 'increased width of mouth', 0.42168674698795183, 7.884497199543557, 1.8234001139933984, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(105231, 'HP:5201010', 'Microform cleft of the upper lip', 'XPO:0141311', 'abnormal roof of mouth morphology', 0.4583333333333333, 7.312692920701687, 1.830751463740579, 'UPHENO:0076800', 'abnormal mouth morphology'),
(105232, 'HP:5201010', 'Microform cleft of the upper lip', 'XPO:0130628', 'increased size of the oral cavity', 0.47297297297297297, 7.884497199543557, 1.9311017790021312, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(105233, 'HP:5201010', 'Microform cleft of the upper lip', 'XPO:0102279', 'abnormal mouth morphology', 0.4782608695652174, 7.312692920701687, 1.8701269676463677, 'UPHENO:0076800', 'abnormal mouth morphology'),
(105234, 'HP:5201010', 'Microform cleft of the upper lip', 'XPO:0103828', 'decreased width of the mouth', 0.42168674698795183, 7.884497199543557, 1.8234001139933984, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(105235, 'HP:0100829', 'Galactorrhea', 'XPO:0128352', 'decreased size of the skeletal system', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(105236, 'HP:0100829', 'Galactorrhea', 'XPO:0102542', 'abnormal vacuolated notochordal tissue morphology', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(105237, 'HP:0100829', 'Galactorrhea', 'XPO:0141699', 'abnormally necrotic anterior notochord', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(105238, 'HP:0100829', 'Galactorrhea', 'XPO:0141719', 'abnormal anterior notochord morphology', 0.45454545454545453, 4.638757693672553, 1.452076521536181, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(105239, 'HP:0100829', 'Galactorrhea', 'XPO:0102217', 'abnormal elastica externa morphology', 0.47619047619047616, 4.638757693672553, 1.4862477031377266, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(105240, 'HP:0100829', 'Galactorrhea', 'XPO:0128580', 'decreased size of the postcranial axial skeleton', 0.4107142857142857, 6.272837960958401, 1.6050994245019483, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(105241, 'HP:0100829', 'Galactorrhea', 'XPO:0102461', 'abnormal postcranial axial skeleton morphology', 0.4791666666666667, 6.272837960958401, 1.7337055275601352, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(105242, 'HP:0100829', 'Galactorrhea', 'XPO:0107372', 'abnormal flexural organ morphology', 0.45454545454545453, 4.638757693672553, 1.452076521536181, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(105243, 'HP:0100829', 'Galactorrhea', 'XPO:0139774', 'abnormally necrotic elastica externa', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(105244, 'HP:0100829', 'Galactorrhea', 'XPO:0130368', 'increased size of the elastica externa', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(105245, 'HP:0100829', 'Galactorrhea', 'XPO:0140350', 'abnormally necrotic notochordal sheath', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(105246, 'HP:0100829', 'Galactorrhea', 'XPO:0102144', 'abnormal cranial skeleton morphology', 0.4375, 6.211345574613551, 1.6484731386629958, 'UPHENO:0087089', 'abnormal axial skeleton plus cranial skeleton morphology'),
(105247, 'HP:0100829', 'Galactorrhea', 'XPO:0126886', 'abnormally localised vertebral column', 0.41818181818181815, 6.272837960958401, 1.6196255072310737, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(105248, 'HP:0100829', 'Galactorrhea', 'XPO:0102216', 'abnormal vertebral column morphology', 0.4423076923076923, 6.272837960958401, 1.6656903922192745, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(105249, 'HP:0100829', 'Galactorrhea', 'XPO:0141703', 'abnormally necrotic posterior notochord', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(105250, 'HP:0100829', 'Galactorrhea', 'XPO:0140683', 'abnormally necrotic flexural organ', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(105251, 'HP:0100829', 'Galactorrhea', 'XPO:0102806', 'abnormal articular system morphology', 0.46511627906976744, 4.638757693672553, 1.4688640910537754, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(105252, 'HP:0100829', 'Galactorrhea', 'XPO:0128890', 'decreased size of the elastica externa', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(105253, 'HP:0100829', 'Galactorrhea', 'XPO:0102980', 'abnormal perichordal tissue morphology', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(105254, 'HP:0100829', 'Galactorrhea', 'XPO:0140510', 'abnormally necrotic postcranial axial skeleton', 0.42592592592592593, 6.272837960958401, 1.6345532468244968, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(105255, 'HP:0100829', 'Galactorrhea', 'XPO:0102093', 'abnormal craniofacial skeleton morphology', 0.42, 6.211345574613551, 1.61516721776344, 'UPHENO:0087089', 'abnormal axial skeleton plus cranial skeleton morphology'),
(105256, 'HP:0100829', 'Galactorrhea', 'XPO:0130060', 'increased size of the postcranial axial skeleton', 0.4107142857142857, 6.272837960958401, 1.6050994245019483, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(105257, 'HP:0100829', 'Galactorrhea', 'XPO:0100584', 'abnormal vertebral column', 0.5, 6.272837960958401, 1.770993783297728, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(105258, 'HP:0100829', 'Galactorrhea', 'XPO:0140432', 'abnormally necrotic skeleton', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(105259, 'HP:0100829', 'Galactorrhea', 'XPO:0140559', 'abnormally necrotic articular system', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(105260, 'HP:0100829', 'Galactorrhea', 'XPO:0102272', 'abnormal notochordal sheath morphology', 0.45454545454545453, 4.638757693672553, 1.452076521536181, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(105261, 'HP:0100829', 'Galactorrhea', 'XPO:0100226', 'abnormal vertebral element', 0.4423076923076923, 6.272837960958401, 1.6656903922192745, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(105262, 'HP:0100829', 'Galactorrhea', 'XPO:0140019', 'abnormally necrotic skeletal system', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(105263, 'HP:0100829', 'Galactorrhea', 'XPO:0102130', 'abnormal endoskeleton morphology', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(105264, 'HP:0100829', 'Galactorrhea', 'XPO:0102567', 'abnormal skeleton morphology', 0.45454545454545453, 4.638757693672553, 1.452076521536181, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(105265, 'HP:0100829', 'Galactorrhea', 'XPO:0102514', 'abnormal perichondrial cell morphology', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(105266, 'HP:0100829', 'Galactorrhea', 'XPO:0102054', 'abnormal notochord morphology', 0.45454545454545453, 4.638757693672553, 1.452076521536181, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(105267, 'HP:0100829', 'Galactorrhea', 'XPO:0102010', 'abnormal perichondrium morphology', 0.4444444444444444, 4.638757693672553, 1.4358516936218344, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(105268, 'HP:0100829', 'Galactorrhea', 'XPO:0102097', 'abnormal skeletal system morphology', 0.47619047619047616, 4.638757693672553, 1.4862477031377266, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(105269, 'HP:0100829', 'Galactorrhea', 'XPO:0101957', 'abnormal axial skeleton morphology', 0.44680851063829785, 6.211345574613551, 1.665917784661915, 'UPHENO:0087089', 'abnormal axial skeleton plus cranial skeleton morphology'),
(105270, 'HP:0100829', 'Galactorrhea', 'XPO:0102605', 'abnormal dermal skeleton morphology', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(105271, 'HP:0100829', 'Galactorrhea', 'XPO:0101860', 'abnormal skeletal subdivision morphology', 0.4444444444444444, 4.638757693672553, 1.4358516936218344, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(105272, 'HP:0100829', 'Galactorrhea', 'XPO:0100693', 'abnormal vertebral centrum', 0.4339622641509434, 6.272837960958401, 1.6499015013598524, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(105273, 'HP:0100829', 'Galactorrhea', 'XPO:0101982', 'abnormal appendicular skeleton morphology', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(105274, 'HP:0100829', 'Galactorrhea', 'XPO:0129832', 'increased size of the skeletal system', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(105275, 'HP:0100829', 'Galactorrhea', 'XPO:0141723', 'abnormal posterior notochord morphology', 0.45454545454545453, 4.638757693672553, 1.452076521536181, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(105276, 'HP:0009765', 'Low hanging columella', 'XPO:0128440', 'decreased size of the Jacobsons organ', 0.4117647058823529, 9.467216006125252, 1.9744025461609567, 'UPHENO:0087950', 'abnormal nose morphology'),
(105277, 'HP:0009765', 'Low hanging columella', 'XPO:0130703', 'increased size of the circumpharyngeal ridge', 0.41379310344827586, 5.972749669260594, 1.572094978607528, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(105278, 'HP:0009765', 'Low hanging columella', 'XPO:0131462', 'increased size of the cilium in olfactory pit', 0.4225352112676056, 9.467216006125252, 2.0000580279742364, 'UPHENO:0087950', 'abnormal nose morphology'),
(105279, 'HP:0009765', 'Low hanging columella', 'XPO:0128846', 'decreased size of the choana', 0.4166666666666667, 9.601025046317446, 2.000106772807959, 'UPHENO:0021517', 'abnormal nose morphology'),
(105280, 'HP:0009765', 'Low hanging columella', 'XPO:0130640', 'increased size of the medial nasal prominence', 0.42105263157894735, 5.972749669260594, 1.585825326448175, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(105281, 'HP:0009765', 'Low hanging columella', 'XPO:0130324', 'increased size of the choana', 0.45714285714285713, 9.601025046317446, 2.0950035850025865, 'UPHENO:0021517', 'abnormal nose morphology'),
(105282, 'HP:0009765', 'Low hanging columella', 'XPO:0103115', 'abnormal nostril morphology', 0.48333333333333334, 9.601025046317446, 2.1541809206873577, 'UPHENO:0021517', 'abnormal nose morphology'),
(105283, 'HP:0009765', 'Low hanging columella', 'XPO:0130319', 'increased size of the craniofacial region', 0.41379310344827586, 5.972749669260594, 1.572094978607528, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(105284, 'HP:0009765', 'Low hanging columella', 'XPO:0103358', 'decreased size of the pharyngeal region', 0.4074074074074074, 4.6864066944795475, 1.3817658272857345, 'UPHENO:0075195', 'abnormal size of anatomical entity'),
(105285, 'HP:0009765', 'Low hanging columella', 'XPO:0142045', 'increased size of the nasal region', 0.41379310344827586, 5.972749669260594, 1.572094978607528, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(105286, 'HP:0009765', 'Low hanging columella', 'XPO:0115526', 'abnormally incomplete structure of head', 0.40384615384615385, 4.5318002188002176, 1.3528303989641963, 'UPHENO:0087907', 'abnormal head morphology'),
(105287, 'HP:0009765', 'Low hanging columella', 'XPO:0102226', 'abnormal Jacobsons organ morphology', 0.4426229508196721, 9.467216006125252, 2.0470483835704494, 'UPHENO:0087950', 'abnormal nose morphology'),
(105288, 'HP:0009765', 'Low hanging columella', 'XPO:0127898', 'abnormally localised nostril', 0.46774193548387094, 9.601025046317446, 2.1191512541094477, 'UPHENO:0021517', 'abnormal nose morphology'),
(105289, 'HP:0009765', 'Low hanging columella', 'XPO:0141839', 'edematous pharyngeal region', 0.40384615384615385, 4.5318002188002176, 1.3528303989641963, 'UPHENO:0087907', 'abnormal head morphology'),
(105290, 'HP:0009765', 'Low hanging columella', 'XPO:0130787', 'increased size of the lateral nasal prominence', 0.42105263157894735, 5.972749669260594, 1.585825326448175, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(105291, 'HP:0009765', 'Low hanging columella', 'XPO:0129460', 'decreased size of the nostril', 0.43478260869565216, 9.601025046317446, 2.043124743081096, 'UPHENO:0021517', 'abnormal nose morphology'),
(105292, 'HP:0009765', 'Low hanging columella', 'XPO:0130273', 'increased size of the pharyngeal pouch', 0.41379310344827586, 5.972749669260594, 1.572094978607528, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(105293, 'HP:0009765', 'Low hanging columella', 'XPO:0102052', 'abnormal choana morphology', 0.43283582089552236, 9.601025046317446, 2.038545451384708, 'UPHENO:0021517', 'abnormal nose morphology'),
(105294, 'HP:0009765', 'Low hanging columella', 'XPO:0133370', 'olfactory pit fused with brain', 0.43548387096774194, 9.467216006125252, 2.030472820215821, 'UPHENO:0087950', 'abnormal nose morphology'),
(105295, 'HP:0009765', 'Low hanging columella', 'XPO:0126871', 'abnormally localised choana', 0.47540983606557374, 9.601025046317446, 2.136450735058322, 'UPHENO:0021517', 'abnormal nose morphology'),
(105296, 'HP:0009765', 'Low hanging columella', 'XPO:0102259', 'abnormal pharyngeal region morphology', 0.42, 4.5318002188002176, 1.3796217205799897, 'UPHENO:0087907', 'abnormal head morphology'),
(105297, 'HP:0009765', 'Low hanging columella', 'XPO:0129920', 'increased size of the Jacobsons organ', 0.46153846153846156, 9.467216006125252, 2.0903311485311, 'UPHENO:0087950', 'abnormal nose morphology'),
(105298, 'HP:0009765', 'Low hanging columella', 'XPO:0101483', 'abnormal nostril', 0.5576923076923077, 9.601025046317446, 2.313961498014265, 'UPHENO:0021517', 'abnormal nose morphology'),
(105299, 'HP:0009765', 'Low hanging columella', 'XPO:0142059', 'abnormal nasal region morphology', 0.40384615384615385, 4.5318002188002176, 1.3528303989641963, 'UPHENO:0087907', 'abnormal head morphology'),
(105300, 'HP:0009765', 'Low hanging columella', 'XPO:0102966', 'abnormal olfactory pit morphology', 0.4576271186440678, 9.467216006125252, 2.0814549676762404, 'UPHENO:0087950', 'abnormal nose morphology'),
(105301, 'HP:0009765', 'Low hanging columella', 'XPO:0130062', 'increased size of the head region', 0.43636363636363634, 5.972749669260594, 1.6144010544992402, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(105302, 'HP:0009765', 'Low hanging columella', 'XPO:0130934', 'increased size of the nostril', 0.48484848484848486, 9.601025046317446, 2.1575547378222804, 'UPHENO:0021517', 'abnormal nose morphology'),
(105303, 'HP:0009765', 'Low hanging columella', 'XPO:0128599', 'decreased size of the olfactory pit', 0.4444444444444444, 9.467216006125252, 2.0512560928070123, 'UPHENO:0087950', 'abnormal nose morphology'),
(105304, 'HP:0009765', 'Low hanging columella', 'XPO:0100420', 'abnormal choana', 0.5370370370370371, 9.601025046317446, 2.2707060671501944, 'UPHENO:0021517', 'abnormal nose morphology'),
(105305, 'HP:0009765', 'Low hanging columella', 'XPO:0126234', 'absent nostril', 0.43283582089552236, 9.601025046317446, 2.038545451384708, 'UPHENO:0021517', 'abnormal nose morphology'),
(105306, 'HP:0009765', 'Low hanging columella', 'XPO:0140593', 'abnormally necrotic Jacobsons organ', 0.4090909090909091, 9.467216006125252, 1.967981707868695, 'UPHENO:0087950', 'abnormal nose morphology'),
(105307, 'HP:0009765', 'Low hanging columella', 'XPO:0101634', 'abnormal head morphology', 0.4117647058823529, 4.5318002188002176, 1.3660290568695288, 'UPHENO:0087907', 'abnormal head morphology'),
(105308, 'HP:0009765', 'Low hanging columella', 'XPO:0133429', 'abnormal cilium morphology in the olfactory pit', 0.40298507462686567, 9.467216006125252, 1.9532400642872965, 'UPHENO:0087950', 'abnormal nose morphology'),
(105309, 'HP:0009765', 'Low hanging columella', 'XPO:0125246', 'absent choana', 0.4393939393939394, 9.601025046317446, 2.053930918342022, 'UPHENO:0021517', 'abnormal nose morphology'),
(105310, 'HP:0009765', 'Low hanging columella', 'XPO:0103739', 'increased size of the pharyngeal region', 0.46153846153846156, 5.972749669260594, 1.6603173472275985, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(105311, 'HP:0009765', 'Low hanging columella', 'XPO:0131638', 'increased size of the intercanthal region', 0.43636363636363634, 5.972749669260594, 1.6144010544992402, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(105312, 'HP:0009765', 'Low hanging columella', 'XPO:0130079', 'increased size of the olfactory pit', 0.4918032786885246, 9.467216006125252, 2.1577784575495413, 'UPHENO:0087950', 'abnormal nose morphology'),
(105313, 'HP:0009125', 'Lipodystrophy', 'XPO:0101448', 'abnormal myelin accumulating cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(105314, 'HP:0009125', 'Lipodystrophy', 'XPO:0100084', 'abnormal anatomical group', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105315, 'HP:0009125', 'Lipodystrophy', 'XPO:0102048', 'abnormal ligament morphology', 0.4166666666666667, 6.985637650836012, 1.70607220085054, 'UPHENO:0002712', 'abnormal connective tissue'),
(105316, 'HP:0009125', 'Lipodystrophy', 'XPO:0100728', 'abnormal cell condensation', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105317, 'HP:0009125', 'Lipodystrophy', 'XPO:0131675', 'abnormal spindle microtubule', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(105318, 'HP:0009125', 'Lipodystrophy', 'XPO:0100638', 'abnormal polar body', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(105319, 'HP:0009125', 'Lipodystrophy', 'XPO:0100899', 'abnormal secondary spermatogonium', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(105320, 'HP:0009125', 'Lipodystrophy', 'XPO:0100031', 'abnormal central nervous system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(105321, 'HP:0009125', 'Lipodystrophy', 'XPO:0100533', 'abnormal melanoblast', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(105322, 'HP:0009125', 'Lipodystrophy', 'XPO:0107260', 'abnormal anterior-posterior axis', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105323, 'HP:0009125', 'Lipodystrophy', 'XPO:0100691', 'abnormal keratin accumulating cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(105324, 'HP:0009125', 'Lipodystrophy', 'XPO:0101976', 'abnormal portion of organism substance morphology', 0.4166666666666667, 2.485033483301678, 1.0175611126818702, 'UPHENO:0076692', 'abnormal anatomical entity morphology'),
(105325, 'HP:0009125', 'Lipodystrophy', 'XPO:0100289', 'abnormal chondroblast', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(105326, 'HP:0009125', 'Lipodystrophy', 'XPO:0115509', 'abnormally semi-viable whole organism', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105327, 'HP:0009125', 'Lipodystrophy', 'XPO:0102049', 'abnormal dense regular connective tissue morphology', 0.45454545454545453, 6.985637650836012, 1.781934297691443, 'UPHENO:0002712', 'abnormal connective tissue'),
(105328, 'HP:0009125', 'Lipodystrophy', 'XPO:0100378', 'abnormal perichondrium', 0.5185185185185185, 6.985637650836012, 1.9032032171102151, 'UPHENO:0002712', 'abnormal connective tissue'),
(105329, 'HP:0009125', 'Lipodystrophy', 'XPO:0101220', 'abnormal centriole', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(105330, 'HP:0009125', 'Lipodystrophy', 'XPO:0101513', 'abnormal basal body', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(105331, 'HP:0009125', 'Lipodystrophy', 'XPO:0100640', 'abnormal notochordal sheath', 0.42857142857142855, 3.9037819259951223, 1.293464107292913, 'HP:0033127', 'Abnormality of the musculoskeletal system'),
(105332, 'HP:0009125', 'Lipodystrophy', 'XPO:0100377', 'abnormal connective tissue', 0.5833333333333334, 6.985637650836012, 2.0186518511920295, 'UPHENO:0002712', 'abnormal connective tissue'),
(105333, 'HP:0009125', 'Lipodystrophy', 'XPO:0100422', 'abnormal notochord', 0.4444444444444444, 3.9037819259951223, 1.3171993734173904, 'HP:0033127', 'Abnormality of the musculoskeletal system'),
(105334, 'HP:0009125', 'Lipodystrophy', 'XPO:0100704', 'abnormal Merkel cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(105335, 'HP:0009125', 'Lipodystrophy', 'XPO:0101096', 'abnormal tendon', 0.5384615384615384, 6.985637650836012, 1.9394579646396068, 'UPHENO:0002712', 'abnormal connective tissue'),
(105336, 'HP:0009125', 'Lipodystrophy', 'XPO:0100481', 'abnormal anatomical line', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105337, 'HP:0009125', 'Lipodystrophy', 'XPO:0100423', 'abnormal process', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105338, 'HP:0009125', 'Lipodystrophy', 'XPO:0101264', 'abnormal mitotic spindle', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(105339, 'HP:0009125', 'Lipodystrophy', 'XPO:0141776', 'abnormal metabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(105340, 'HP:0009125', 'Lipodystrophy', 'XPO:0125009', 'absent connective tissue', 0.4117647058823529, 6.985637650836012, 1.6960067902862834, 'UPHENO:0002712', 'abnormal connective tissue'),
(105341, 'HP:0009125', 'Lipodystrophy', 'XPO:0101409', 'abnormal perivitelline space', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(105342, 'HP:0009125', 'Lipodystrophy', 'XPO:0100573', 'abnormal extraembryonic structure', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105343, 'HP:0009125', 'Lipodystrophy', 'XPO:0103125', 'abnormal fat body morphology', 0.40476190476190477, 10.114017760664272, 2.0233064754510637, 'HP:0009124', 'Abnormal adipose tissue morphology'),
(105344, 'HP:0009125', 'Lipodystrophy', 'XPO:0101237', 'abnormal mucus secreting cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(105345, 'HP:0009125', 'Lipodystrophy', 'XPO:0101221', 'abnormal larval immune system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(105346, 'HP:0009125', 'Lipodystrophy', 'XPO:0141714', 'abnormal anterior notochord', 0.42857142857142855, 3.9037819259951223, 1.293464107292913, 'HP:0033127', 'Abnormality of the musculoskeletal system'),
(105347, 'HP:0009125', 'Lipodystrophy', 'XPO:0102794', 'abnormal stromal cell morphology', 0.4166666666666667, 6.985637650836012, 1.70607220085054, 'UPHENO:0002712', 'abnormal connective tissue'),
(105348, 'HP:0009125', 'Lipodystrophy', 'XPO:0101468', 'abnormal stage I oocyte', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(105349, 'HP:0009125', 'Lipodystrophy', 'XPO:0100724', 'abnormal kinetochore', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(105350, 'HP:0009125', 'Lipodystrophy', 'XPO:0101071', 'abnormal endoplasmic reticulum', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(105351, 'HP:0009125', 'Lipodystrophy', 'XPO:0107284', 'abnormal migrating myoblast', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(105352, 'HP:0009125', 'Lipodystrophy', 'XPO:0107259', 'abnormal animal-vegetal axis', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105353, 'HP:0009125', 'Lipodystrophy', 'XPO:0100976', 'abnormal multiciliated cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(105354, 'HP:0009125', 'Lipodystrophy', 'XPO:0101569', 'abnormal activin-induced ectoderm', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105355, 'HP:0009125', 'Lipodystrophy', 'XPO:0101348', 'abnormal perichordal tissue', 0.4827586206896552, 6.985637650836012, 1.836403222866731, 'UPHENO:0002712', 'abnormal connective tissue'),
(105356, 'HP:0009125', 'Lipodystrophy', 'XPO:0131666', 'abnormal adherens junction', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(105357, 'HP:0009125', 'Lipodystrophy', 'XPO:0100274', 'abnormal sensory system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(105358, 'HP:0009125', 'Lipodystrophy', 'XPO:0101547', 'abnormal lampbrush chromosome', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(105359, 'HP:0009125', 'Lipodystrophy', 'XPO:0100081', 'abnormal anatomical entity in vitro', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105360, 'HP:0009125', 'Lipodystrophy', 'XPO:0107258', 'abnormal anatomical axis', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105361, 'HP:0009125', 'Lipodystrophy', 'XPO:0100337', 'abnormal zygote', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(105362, 'HP:0009125', 'Lipodystrophy', 'XPO:0101480', 'abnormal stage V oocyte', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(105363, 'HP:0009125', 'Lipodystrophy', 'XPO:0101113', 'abnormal stage IV oocyte', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(105364, 'HP:0009125', 'Lipodystrophy', 'XPO:0101713', 'abnormal anatomical entity in vitro morphology', 0.4166666666666667, 2.485033483301678, 1.0175611126818702, 'UPHENO:0076692', 'abnormal anatomical entity morphology'),
(105365, 'HP:0009125', 'Lipodystrophy', 'XPO:0100545', 'abnormal male organism', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105366, 'HP:0009125', 'Lipodystrophy', 'XPO:0100025', 'abnormal oocyte', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(105367, 'HP:0009125', 'Lipodystrophy', 'XPO:0100465', 'abnormal skeletal system', 0.4444444444444444, 3.9037819259951223, 1.3171993734173904, 'HP:0033127', 'Abnormality of the musculoskeletal system'),
(105368, 'HP:0009125', 'Lipodystrophy', 'XPO:0100674', 'abnormal secondary oogonium', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(105369, 'HP:0009125', 'Lipodystrophy', 'XPO:0100416', 'abnormal ligament', 0.5384615384615384, 6.985637650836012, 1.9394579646396068, 'UPHENO:0002712', 'abnormal connective tissue'),
(105370, 'HP:0009125', 'Lipodystrophy', 'XPO:0100581', 'abnormal immune system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(105371, 'HP:0009125', 'Lipodystrophy', 'XPO:0100285', 'abnormal progenitor cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(105372, 'HP:0009125', 'Lipodystrophy', 'XPO:0100501', 'abnormal urogenital system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(105373, 'HP:0009125', 'Lipodystrophy', 'XPO:0100437', 'abnormal proepicardium', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(105374, 'HP:0009125', 'Lipodystrophy', 'XPO:0102009', 'abnormal connective tissue morphology', 0.4838709677419355, 6.985637650836012, 1.8385176774794747, 'UPHENO:0002712', 'abnormal connective tissue'),
(105375, 'HP:0009125', 'Lipodystrophy', 'XPO:0100754', 'abnormal electrically active cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(105376, 'HP:0009125', 'Lipodystrophy', 'XPO:0131677', 'abnormal actin filament', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(105377, 'HP:0009125', 'Lipodystrophy', 'XPO:0100108', 'abnormal cell part', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(105378, 'HP:0009125', 'Lipodystrophy', 'XPO:0101435', 'abnormal paracrine cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(105379, 'HP:0009125', 'Lipodystrophy', 'XPO:0101061', 'abnormal plasma membrane', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(105380, 'HP:0009125', 'Lipodystrophy', 'XPO:0101638', 'abnormal anatomical structure morphology', 0.4166666666666667, 2.485033483301678, 1.0175611126818702, 'UPHENO:0076692', 'abnormal anatomical entity morphology'),
(105381, 'HP:0009125', 'Lipodystrophy', 'XPO:0101326', 'abnormal cementoblast', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(105382, 'HP:0009125', 'Lipodystrophy', 'XPO:0107261', 'abnormal dorsal-ventral axis', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105383, 'HP:0009125', 'Lipodystrophy', 'XPO:0115508', 'abnormally peramorphic growth of whole organism', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105384, 'HP:0009125', 'Lipodystrophy', 'XPO:0101110', 'abnormal cell-free extract', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105385, 'HP:0009125', 'Lipodystrophy', 'XPO:0101602', 'abnormal intersomitic tendon', 0.4827586206896552, 6.985637650836012, 1.836403222866731, 'UPHENO:0002712', 'abnormal connective tissue'),
(105386, 'HP:0009125', 'Lipodystrophy', 'XPO:0100417', 'abnormal dense regular connective tissue', 0.56, 6.985637650836012, 1.9778668014980603, 'UPHENO:0002712', 'abnormal connective tissue'),
(105387, 'HP:0009125', 'Lipodystrophy', 'XPO:0100549', 'abnormal mitotic cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(105388, 'HP:0009125', 'Lipodystrophy', 'XPO:0100599', 'abnormal adult immune system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(105389, 'HP:0009125', 'Lipodystrophy', 'XPO:0100791', 'abnormal multiciliated cell precursor', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(105390, 'HP:0009125', 'Lipodystrophy', 'XPO:0101141', 'abnormal Keller explant', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105391, 'HP:0009125', 'Lipodystrophy', 'XPO:0100239', 'abnormal acellular anatomical structure', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105392, 'HP:0009125', 'Lipodystrophy', 'XPO:0101241', 'abnormal nucleate erythrocyte', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(105393, 'HP:0009125', 'Lipodystrophy', 'XPO:0115491', 'abnormally increased distribution of connective tissue', 0.46875, 6.985637650836012, 1.8095628336229115, 'UPHENO:0002712', 'abnormal connective tissue'),
(105394, 'HP:0009125', 'Lipodystrophy', 'XPO:0100721', 'abnormal centromere', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(105395, 'HP:0009125', 'Lipodystrophy', 'XPO:0100372', 'abnormal hematological system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(105396, 'HP:0009125', 'Lipodystrophy', 'XPO:0100307', 'abnormal blastomere', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(105397, 'HP:0009125', 'Lipodystrophy', 'XPO:0101157', 'abnormal female organism', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105398, 'HP:0009125', 'Lipodystrophy', 'XPO:0101109', 'abnormal egg cell-free extract', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105399, 'HP:0009125', 'Lipodystrophy', 'XPO:0131667', 'abnormal actin cytoskeleton', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(105400, 'HP:0009125', 'Lipodystrophy', 'XPO:0141315', 'abnormal anatomical region', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105401, 'HP:0009125', 'Lipodystrophy', 'XPO:0101004', 'abnormal acid secreting cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(105402, 'HP:0009125', 'Lipodystrophy', 'XPO:0101467', 'abnormal alkali secreting cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(105403, 'HP:0009125', 'Lipodystrophy', 'XPO:0101162', 'abnormal stromal cell', 0.5, 6.985637650836012, 1.8689084582766504, 'UPHENO:0002712', 'abnormal connective tissue'),
(105404, 'HP:0009125', 'Lipodystrophy', 'XPO:0100802', 'abnormal exocrine cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(105405, 'HP:0009125', 'Lipodystrophy', 'XPO:0101493', 'abnormal fat body', 0.4666666666666667, 6.985637650836012, 1.805537104868467, 'UPHENO:0002712', 'abnormal connective tissue'),
(105406, 'HP:0009125', 'Lipodystrophy', 'XPO:0101461', 'abnormal sperm entry point', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(105407, 'HP:0009125', 'Lipodystrophy', 'XPO:00000000', 'Xenopus phenotype', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(105408, 'HP:0009125', 'Lipodystrophy', 'XPO:0101498', 'abnormal stage II oocyte', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(105409, 'HP:0009125', 'Lipodystrophy', 'XPO:0100032', 'abnormal nervous system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(105410, 'HP:0009125', 'Lipodystrophy', 'XPO:0100956', 'abnormal centrosome', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(105411, 'HP:0009125', 'Lipodystrophy', 'XPO:0100062', 'abnormal anatomical space', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105412, 'HP:0009125', 'Lipodystrophy', 'XPO:0100232', 'abnormal lymphatic system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(105413, 'HP:0009125', 'Lipodystrophy', 'XPO:0100653', 'abnormal myoblast', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(105414, 'HP:0009125', 'Lipodystrophy', 'XPO:0100429', 'abnormal spermatid', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(105415, 'HP:0009125', 'Lipodystrophy', 'XPO:0128573', 'decreased size of the adipose tissue', 0.4146341463414634, 10.114017760664272, 2.047832297888533, 'HP:0009124', 'Abnormal adipose tissue morphology'),
(105416, 'HP:0009125', 'Lipodystrophy', 'XPO:0100477', 'abnormal pericyte', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(105417, 'HP:0009125', 'Lipodystrophy', 'XPO:0142057', 'abnormal desmosome', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(105418, 'HP:0009125', 'Lipodystrophy', 'XPO:0101132', 'abnormal apoptotic cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(105419, 'HP:0009125', 'Lipodystrophy', 'XPO:0100688', 'abnormal adipose tissue', 0.56, 6.985637650836012, 1.9778668014980603, 'UPHENO:0002712', 'abnormal connective tissue'),
(105420, 'HP:0009125', 'Lipodystrophy', 'XPO:0101297', 'abnormal barrier cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(105421, 'HP:0009125', 'Lipodystrophy', 'XPO:0130053', 'increased size of the adipose tissue', 0.4146341463414634, 10.114017760664272, 2.047832297888533, 'UPHENO:0076797', 'abnormal adipose tissue morphology'),
(105422, 'HP:0009125', 'Lipodystrophy', 'XPO:0141499', 'abnormal tadpole', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105423, 'HP:0009125', 'Lipodystrophy', 'XPO:0100626', 'abnormal primordial germ cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(105424, 'HP:0009125', 'Lipodystrophy', 'XPO:0102010', 'abnormal perichondrium morphology', 0.40540540540540543, 6.985637650836012, 1.6828592525379054, 'UPHENO:0002712', 'abnormal connective tissue'),
(105425, 'HP:0009125', 'Lipodystrophy', 'XPO:0100258', 'abnormal organ part', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105426, 'HP:0009125', 'Lipodystrophy', 'XPO:0100715', 'abnormal ciliated cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(105427, 'HP:0009125', 'Lipodystrophy', 'XPO:0100585', 'abnormal elastica externa', 0.46153846153846156, 3.9037819259951223, 1.3422911399191462, 'HP:0033127', 'Abnormality of the musculoskeletal system'),
(105428, 'HP:0009125', 'Lipodystrophy', 'XPO:0100546', 'abnormal whole organism', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105429, 'HP:0009125', 'Lipodystrophy', 'XPO:0100344', 'abnormal portion of organism substance', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105430, 'HP:0009125', 'Lipodystrophy', 'XPO:0100308', 'abnormal early embryonic cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(105431, 'HP:0009125', 'Lipodystrophy', 'XPO:0141718', 'abnormal posterior notochord', 0.42857142857142855, 3.9037819259951223, 1.293464107292913, 'HP:0033127', 'Abnormality of the musculoskeletal system'),
(105432, 'HP:0009125', 'Lipodystrophy', 'XPO:0102320', 'abnormal adipose tissue morphology', 0.5151515151515151, 10.114017760664272, 2.28259754965161, 'UPHENO:0076797', 'abnormal adipose tissue morphology'),
(105433, 'HP:0009125', 'Lipodystrophy', 'XPO:0101333', 'abnormal barrier epithelial cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(105434, 'HP:0009125', 'Lipodystrophy', 'XPO:0107312', 'abnormal filopodium', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(105435, 'HP:0009125', 'Lipodystrophy', 'XPO:0140339', 'abnormally necrotic adipose tissue', 0.425, 10.114017760664272, 2.0732721838394292, 'UPHENO:0076797', 'abnormal adipose tissue morphology'),
(105436, 'HP:0009125', 'Lipodystrophy', 'XPO:0100910', 'abnormal vacuolated notochordal tissue', 0.4827586206896552, 6.985637650836012, 1.836403222866731, 'UPHENO:0002712', 'abnormal connective tissue'),
(105437, 'HP:0009125', 'Lipodystrophy', 'XPO:0100969', 'abnormal disaggregated/reaggregated ectoderm treated with activin', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105438, 'HP:0009125', 'Lipodystrophy', 'XPO:0131685', 'abnormal cortical actin cytoskeleton', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(105439, 'HP:0009125', 'Lipodystrophy', 'XPO:0101472', 'abnormal zygote cortex', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(105440, 'HP:0009125', 'Lipodystrophy', 'XPO:0100852', 'abnormal interdigital region', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(105441, 'HP:0009125', 'Lipodystrophy', 'XPO:0100515', 'abnormal somatic stem cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(105442, 'HP:0009125', 'Lipodystrophy', 'XPO:0101240', 'abnormal ciliated non-epidermal cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(105443, 'HP:0009125', 'Lipodystrophy', 'XPO:0100917', 'abnormal stage III oocyte', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(105444, 'HP:0009125', 'Lipodystrophy', 'XPO:0100902', 'abnormal spermatocyte', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(105445, 'HP:0009125', 'Lipodystrophy', 'XPO:0100993', 'abnormal ligament cell', 0.4666666666666667, 6.985637650836012, 1.805537104868467, 'UPHENO:0002712', 'abnormal connective tissue'),
(105446, 'HP:0009125', 'Lipodystrophy', 'XPO:0107285', 'abnormal flexural organ', 0.42857142857142855, 3.9037819259951223, 1.293464107292913, 'HP:0033127', 'Abnormality of the musculoskeletal system'),
(105447, 'HP:0009125', 'Lipodystrophy', 'XPO:0100574', 'abnormal gastrula cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(105448, 'HP:0009125', 'Lipodystrophy', 'XPO:0101174', 'abnormal articular system', 0.42857142857142855, 3.9037819259951223, 1.293464107292913, 'HP:0033127', 'Abnormality of the musculoskeletal system'),
(105449, 'HP:0009125', 'Lipodystrophy', 'XPO:0107262', 'abnormal left-right axis', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105450, 'HP:0009125', 'Lipodystrophy', 'XPO:0115505', 'dead whole organism', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105451, 'HP:0009125', 'Lipodystrophy', 'XPO:0139793', 'abnormally necrotic connective tissue', 0.4166666666666667, 6.985637650836012, 1.70607220085054, 'UPHENO:0002712', 'abnormal connective tissue'),
(105452, 'HP:0009125', 'Lipodystrophy', 'XPO:0100894', 'abnormal nucleus', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(105453, 'HP:0009125', 'Lipodystrophy', 'XPO:0101535', 'abnormal absorptive cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(105454, 'HP:0009125', 'Lipodystrophy', 'XPO:0100202', 'abnormal embryo', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105455, 'HP:0009125', 'Lipodystrophy', 'XPO:0100006', 'abnormal anatomical structure', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105456, 'HP:0009125', 'Lipodystrophy', 'XPO:0100225', 'abnormal endocrine system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(105457, 'HP:0009125', 'Lipodystrophy', 'XPO:0100386', 'abnormal limb', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(105458, 'HP:0009125', 'Lipodystrophy', 'XPO:0126626', 'abnormally localised connective tissue', 0.4117647058823529, 6.985637650836012, 1.6960067902862834, 'UPHENO:0002712', 'abnormal connective tissue'),
(105459, 'HP:0009125', 'Lipodystrophy', 'XPO:0100392', 'abnormal cilium', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(105460, 'HP:0009125', 'Lipodystrophy', 'XPO:0100882', 'abnormal perichondrial cell', 0.45161290322580644, 6.985637650836012, 1.7761768212589517, 'UPHENO:0002712', 'abnormal connective tissue'),
(105461, 'HP:0009125', 'Lipodystrophy', 'XPO:0100172', 'abnormal stem cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(105462, 'HP:0009125', 'Lipodystrophy', 'XPO:0100317', 'abnormal respiratory system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(105463, 'HP:0009125', 'Lipodystrophy', 'XPO:0100907', 'abnormal cytoplasm', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(105464, 'HP:0009125', 'Lipodystrophy', 'XPO:0100004', 'abnormal cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(105465, 'HP:0009125', 'Lipodystrophy', 'XPO:0107253', 'abnormal enteric nervous system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(105466, 'HP:0009125', 'Lipodystrophy', 'XPO:0102113', 'abnormal anatomical line morphology', 0.4166666666666667, 2.485033483301678, 1.0175611126818702, 'UPHENO:0076692', 'abnormal anatomical entity morphology'),
(105467, 'HP:0009125', 'Lipodystrophy', 'XPO:0101228', 'abnormal mesenchymal stem cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(105468, 'HP:0009125', 'Lipodystrophy', 'XPO:0100026', 'abnormal germ cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(105469, 'HP:0009125', 'Lipodystrophy', 'XPO:0100935', 'abnormal skeleton', 0.41379310344827586, 3.9037819259951223, 1.270967363209146, 'HP:0033127', 'Abnormality of the musculoskeletal system'),
(105470, 'HP:0009125', 'Lipodystrophy', 'XPO:0115512', 'abnormally semi-erect whole organism', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105471, 'HP:0009125', 'Lipodystrophy', 'XPO:0100010', 'abnormal multicellular anatomical structure', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105472, 'HP:0009125', 'Lipodystrophy', 'XPO:0101366', 'abnormal morula cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(105473, 'HP:0009125', 'Lipodystrophy', 'XPO:0107270', 'abnormal proximal-distal axis', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105474, 'HP:0009125', 'Lipodystrophy', 'XPO:0101373', 'abnormal oxygen accumulating cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(105475, 'HP:0009125', 'Lipodystrophy', 'XPO:0100176', 'abnormal stage VI oocyte', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(105476, 'HP:0009125', 'Lipodystrophy', 'XPO:0100888', 'abnormal microtubule', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(105477, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100858', 'abnormal presumptive midbrain-hindbrain boundary', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(105478, 'HP:0032479', 'Preimplantation lethality', 'XPO:0107265', 'abnormal posterior side', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105479, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100255', 'abnormal pelvic appendage', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105480, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100189', 'abnormal enteroendocrine cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(105481, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100376', 'abnormal animal pole', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105482, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100258', 'abnormal organ part', 0.5294117647058824, 1.706362323152461, 0.9504568842024205, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105483, 'HP:0032479', 'Preimplantation lethality', 'XPO:0101040', 'abnormal axial mesoderm', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105484, 'HP:0032479', 'Preimplantation lethality', 'XPO:0101377', 'abnormal manicotto glandulare', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(105485, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100403', 'abnormal forelimb', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(105486, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100642', 'abnormal gustatory system', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(105487, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100574', 'abnormal gastrula cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(105488, 'HP:0032479', 'Preimplantation lethality', 'XPO:0101519', 'abnormal hypobranchial placode', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105489, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100888', 'abnormal microtubule', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(105490, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100004', 'abnormal cell', 0.55, 1.8210412618256888, 1.0007860380741376, 'HP:0000118', 'Phenotypic abnormality'),
(105491, 'HP:0032479', 'Preimplantation lethality', 'XPO:0101589', 'abnormal blastocoel roof', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105492, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100120', 'abnormal genital system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(105493, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100308', 'abnormal early embryonic cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(105494, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100999', 'abnormal serous membrane', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105495, 'HP:0032479', 'Preimplantation lethality', 'XPO:0101349', 'abnormal trunk region', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105496, 'HP:0032479', 'Preimplantation lethality', 'XPO:0141784', 'abnormal cellular hormone metabolic process', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(105497, 'HP:0032479', 'Preimplantation lethality', 'XPO:0101435', 'abnormal paracrine cell', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(105498, 'HP:0032479', 'Preimplantation lethality', 'XPO:0101224', 'abnormal dorsal involuting marginal zone', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105499, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100468', 'abnormal muscular system', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105500, 'HP:0032479', 'Preimplantation lethality', 'XPO:0101264', 'abnormal mitotic spindle', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(105501, 'HP:0032479', 'Preimplantation lethality', 'XPO:0141796', 'abnormal demethylation', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(105502, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100285', 'abnormal progenitor cell', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(105503, 'HP:0032479', 'Preimplantation lethality', 'XPO:0107267', 'abnormal ventral side', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105504, 'HP:0032479', 'Preimplantation lethality', 'XPO:0101560', 'abnormal compound organ component', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105505, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100599', 'abnormal adult immune system', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(105506, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100026', 'abnormal germ cell', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(105507, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100482', 'abnormal Mullerian duct', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(105508, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100868', 'abnormal transporting epithelium', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105509, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100688', 'abnormal adipose tissue', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(105510, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100917', 'abnormal stage III oocyte', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(105511, 'HP:0032479', 'Preimplantation lethality', 'XPO:0141276', 'decreased surface breathing', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(105512, 'HP:0032479', 'Preimplantation lethality', 'XPO:0141782', 'abnormal methylation', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(105513, 'HP:0032479', 'Preimplantation lethality', 'XPO:0101373', 'abnormal oxygen accumulating cell', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(105514, 'HP:0032479', 'Preimplantation lethality', 'XPO:0125007', 'absent anatomical line', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105515, 'HP:0032479', 'Preimplantation lethality', 'XPO:0101113', 'abnormal stage IV oocyte', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(105516, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100422', 'abnormal notochord', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(105517, 'HP:0032479', 'Preimplantation lethality', 'XPO:0101240', 'abnormal ciliated non-epidermal cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(105518, 'HP:0032479', 'Preimplantation lethality', 'XPO:0101480', 'abnormal stage V oocyte', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(105519, 'HP:0032479', 'Preimplantation lethality', 'XPO:0115758', 'abnormally decreased mobility of melanoblast', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(105520, 'HP:0032479', 'Preimplantation lethality', 'XPO:0107260', 'abnormal anterior-posterior axis', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105521, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100100', 'abnormal muscle', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(105522, 'HP:0032479', 'Preimplantation lethality', 'XPO:0131685', 'abnormal cortical actin cytoskeleton', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(105523, 'HP:0032479', 'Preimplantation lethality', 'XPO:0127101', 'abnormally localised portion of organism substance', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105524, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100187', 'abnormal regenerating limb', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105525, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100251', 'abnormal proteinaceous extracellular matrix', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105526, 'HP:0032479', 'Preimplantation lethality', 'XPO:0141266', 'abnormal surface breathing', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(105527, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100722', 'abnormal barbel', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105528, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100415', 'abnormal secretory epithelial cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(105529, 'HP:0032479', 'Preimplantation lethality', 'XPO:0101149', 'abnormal amputated limb', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105530, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100974', 'abnormal cardiac mesoderm', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105531, 'HP:0032479', 'Preimplantation lethality', 'XPO:0101221', 'abnormal larval immune system', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(105532, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100377', 'abnormal connective tissue', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(105533, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100067', 'abnormal animal hemisphere', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105534, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100546', 'abnormal whole organism', 0.5294117647058824, 1.706362323152461, 0.9504568842024205, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105535, 'HP:0032479', 'Preimplantation lethality', 'XPO:0141267', 'abnormal resting posture', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(105536, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100902', 'abnormal spermatocyte', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(105537, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100493', 'abnormal liver and biliary system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(105538, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100674', 'abnormal secondary oogonium', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(105539, 'HP:0032479', 'Preimplantation lethality', 'XPO:0141754', 'abnormal homeostatic process', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(105540, 'HP:0032479', 'Preimplantation lethality', 'XPO:0101071', 'abnormal endoplasmic reticulum', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(105541, 'HP:0032479', 'Preimplantation lethality', 'XPO:0101347', 'abnormal hindlimb region', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105542, 'HP:0032479', 'Preimplantation lethality', 'XPO:0141497', 'abnormal lymphoblast', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(105543, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100293', 'abnormal duct', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105544, 'HP:0032479', 'Preimplantation lethality', 'XPO:0131729', 'abnormal regulation of growth rate', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(105545, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100807', 'abnormal matrix-based tissue', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105546, 'HP:0032479', 'Preimplantation lethality', 'XPO:0141795', 'abnormal glycosylation', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(105547, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100856', 'abnormal simple organ', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105548, 'HP:0032479', 'Preimplantation lethality', 'XPO:0101157', 'abnormal female organism', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105549, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100458', 'abnormal autopod', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(105550, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100028', 'abnormal anatomical cluster', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105551, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100060', 'abnormal regenerating tissue', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105552, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100862', 'abnormal blastomere V1', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(105553, 'HP:0032479', 'Preimplantation lethality', 'XPO:0115505', 'dead whole organism', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105554, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100954', 'abnormal neural progenitor cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(105555, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100317', 'abnormal respiratory system', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(105556, 'HP:0032479', 'Preimplantation lethality', 'XPO:0115473', 'abnormally delayed phase of Mullerian duct', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(105557, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100796', 'abnormal pseudoblastema', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105558, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100553', 'abnormal laryngeal muscle primordium', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105559, 'HP:0032479', 'Preimplantation lethality', 'XPO:0101403', 'abnormal basal lamina', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105560, 'HP:0032479', 'Preimplantation lethality', 'XPO:0107262', 'abnormal left-right axis', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105561, 'HP:0032479', 'Preimplantation lethality', 'XPO:0115391', 'abnormally undifferentiated alimentary system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(105562, 'HP:0032479', 'Preimplantation lethality', 'XPO:0101326', 'abnormal cementoblast', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(105563, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100551', 'abnormal oocyte cortex', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(105564, 'HP:0032479', 'Preimplantation lethality', 'XPO:0101468', 'abnormal stage I oocyte', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(105565, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100449', 'abnormal lymphocyte', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(105566, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100265', 'abnormal sensory epithelial cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(105567, 'HP:0032479', 'Preimplantation lethality', 'XPO:0107288', 'abnormal larval alimentary system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(105568, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100521', 'abnormal animal blastomere', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(105569, 'HP:0032479', 'Preimplantation lethality', 'XPO:0115512', 'abnormally semi-erect whole organism', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105570, 'HP:0032479', 'Preimplantation lethality', 'XPO:0128000', 'absent behavior', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(105571, 'HP:0032479', 'Preimplantation lethality', 'XPO:0107271', 'abnormal apical region', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105572, 'HP:0032479', 'Preimplantation lethality', 'XPO:0115566', 'abnormal variability of size of forelimb', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(105573, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100032', 'abnormal nervous system', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(105574, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100309', 'abnormal vegetal hemisphere', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105575, 'HP:0032479', 'Preimplantation lethality', 'XPO:0115574', 'abnormal variability of size of hindlimb', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(105576, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100433', 'abnormal pectoral appendage', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105577, 'HP:0032479', 'Preimplantation lethality', 'XPO:0141841', 'abnormality of whole organism mass', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(105578, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100665', 'abnormal egg jelly', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105579, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100523', 'abnormal midgut', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(105580, 'HP:0032479', 'Preimplantation lethality', 'XPO:0107258', 'abnormal anatomical axis', 0.5294117647058824, 1.706362323152461, 0.9504568842024205, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105581, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100935', 'abnormal skeleton', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(105582, 'HP:0032479', 'Preimplantation lethality', 'XPO:0101107', 'abnormal erythroid cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(105583, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100332', 'abnormal germinal granule', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(105584, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100531', 'abnormal proliferative region', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105585, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100486', 'abnormal oral evagination', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(105586, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100612', 'abnormal unilaminar epithelium', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105587, 'HP:0032479', 'Preimplantation lethality', 'XPO:0101297', 'abnormal barrier cell', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(105588, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100588', 'abnormal unicellular gland', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105589, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100108', 'abnormal cell part', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(105590, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100481', 'abnormal anatomical line', 0.5625, 1.706362323152461, 0.9797085315405084, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105591, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100860', 'abnormal parathyroid', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(105592, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100653', 'abnormal myoblast', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(105593, 'HP:0032479', 'Preimplantation lethality', 'XPO:0141271', 'increased surface breathing', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(105594, 'HP:0032479', 'Preimplantation lethality', 'XPO:0142057', 'abnormal desmosome', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(105595, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100742', 'abnormal musculoskeletal system', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105596, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100702', 'abnormal glial cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(105597, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100003', 'abnormal organism subdivision', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105598, 'HP:0032479', 'Preimplantation lethality', 'XPO:0107312', 'abnormal filopodium', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(105599, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100664', 'abnormal periocular region', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(105600, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100786', 'abnormal presumptive axial mesoderm', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105601, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100537', 'abnormal medium cavity', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(105602, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100164', 'abnormal neural nucleus', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(105603, 'HP:0032479', 'Preimplantation lethality', 'XPO:0133388', 'absent insulin receptor signaling pathway', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(105604, 'HP:0032479', 'Preimplantation lethality', 'XPO:0141778', 'abnormal biosynthetic process', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(105605, 'HP:0032479', 'Preimplantation lethality', 'XPO:0141792', 'abnormal small molecule metabolic process', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(105606, 'HP:0032479', 'Preimplantation lethality', 'XPO:0101406', 'abnormal cleavage furrow', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105607, 'HP:0032479', 'Preimplantation lethality', 'XPO:0141791', 'abnormal primary metabolic process', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(105608, 'HP:0032479', 'Preimplantation lethality', 'XPO:0101463', 'abnormal right-ventral blastomere', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(105609, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100363', 'abnormal cardiovascular system', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105610, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100887', 'abnormal right-dorsal blastomere', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(105611, 'HP:0032479', 'Preimplantation lethality', 'XPO:0101004', 'abnormal acid secreting cell', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(105612, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100175', 'abnormal migrating neuroblast', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(105613, 'HP:0032479', 'Preimplantation lethality', 'XPO:0101577', 'abnormal notochordal epithelium', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105614, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100549', 'abnormal mitotic cell', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(105615, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100273', 'abnormal visual system', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(105616, 'HP:0032479', 'Preimplantation lethality', 'XPO:0107285', 'abnormal flexural organ', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(105617, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100991', 'abnormal iliac process primordium', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105618, 'HP:0032479', 'Preimplantation lethality', 'XPO:0142056', 'abnormal main body axis', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105619, 'HP:0032479', 'Preimplantation lethality', 'XPO:0101187', 'abnormal dorsolateral commissural neuron', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(105620, 'HP:0032479', 'Preimplantation lethality', 'XPO:0115509', 'abnormally semi-viable whole organism', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105621, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100437', 'abnormal proepicardium', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(105622, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100423', 'abnormal process', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105623, 'HP:0032479', 'Preimplantation lethality', 'XPO:0101467', 'abnormal alkali secreting cell', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(105624, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100295', 'abnormal extracellular matrix', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105625, 'HP:0032479', 'Preimplantation lethality', 'XPO:0107326', 'abnormal regenerating pelvic girdle', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105626, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100152', 'abnormal alimentary system', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(105627, 'HP:0032479', 'Preimplantation lethality', 'XPO:0101424', 'abnormal coelomic epithelium', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105628, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100802', 'abnormal exocrine cell', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(105629, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100231', 'abnormal compound organ', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105630, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100203', 'abnormal endocrine cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(105631, 'HP:0032479', 'Preimplantation lethality', 'XPO:0101368', 'abnormal regenerating eye', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105632, 'HP:0032479', 'Preimplantation lethality', 'XPO:0101587', 'abnormal hemangioblast', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(105633, 'HP:0032479', 'Preimplantation lethality', 'XPO:0107264', 'abnormal anterior side', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105634, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100239', 'abnormal acellular anatomical structure', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105635, 'HP:0032479', 'Preimplantation lethality', 'XPO:0101311', 'abnormal bottle cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(105636, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100031', 'abnormal central nervous system', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(105637, 'HP:0032479', 'Preimplantation lethality', 'XPO:0141743', 'abnormal chemical homeostasis within a tissue', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(105638, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100900', 'abnormal angioblast', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(105639, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100581', 'abnormal immune system', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(105640, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100610', 'abnormal appendage', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105641, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100084', 'abnormal anatomical group', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105642, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100009', 'abnormal multi-tissue structure', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105643, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100014', 'abnormal tissue', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105644, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100378', 'abnormal perichondrium', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(105645, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100501', 'abnormal urogenital system', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(105646, 'HP:0032479', 'Preimplantation lethality', 'XPO:0126321', 'abnormally localised anatomical structure', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105647, 'HP:0032479', 'Preimplantation lethality', 'XPO:0131723', 'abnormal pathway-restricted SMAD protein phosphorylation', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(105648, 'HP:0032479', 'Preimplantation lethality', 'XPO:0131669', 'abnormal Roux spot', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(105649, 'HP:0032479', 'Preimplantation lethality', 'XPO:0101302', 'abnormal subcortical cytoplasm', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(105650, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100643', 'abnormal thoracic region', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105651, 'HP:0032479', 'Preimplantation lethality', 'XPO:0141907', 'abnormal putrescine metabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(105652, 'HP:0032479', 'Preimplantation lethality', 'XPO:0101109', 'abnormal egg cell-free extract', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105653, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100605', 'abnormal prechordal plate', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105654, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100872', 'abnormal neuroendocrine cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(105655, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100638', 'abnormal polar body', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(105656, 'HP:0032479', 'Preimplantation lethality', 'XPO:0101533', 'abnormal simple cuboidal epithelium', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105657, 'HP:0032479', 'Preimplantation lethality', 'XPO:0101269', 'abnormal mesodermal cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(105658, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100151', 'abnormal primordium', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105659, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100587', 'abnormal vestibuloauditory system', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(105660, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100427', 'abnormal olfactory system', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(105661, 'HP:0032479', 'Preimplantation lethality', 'XPO:0101237', 'abnormal mucus secreting cell', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(105662, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100509', 'abnormal germ plasm', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(105663, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100842', 'abnormal left-dorsal blastomere', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(105664, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100277', 'abnormal blastocoel', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105665, 'HP:0032479', 'Preimplantation lethality', 'XPO:0107270', 'abnormal proximal-distal axis', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105666, 'HP:0032479', 'Preimplantation lethality', 'XPO:0101460', 'abnormal fibrocellular pad', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105667, 'HP:0032479', 'Preimplantation lethality', 'XPO:0101513', 'abnormal basal body', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(105668, 'HP:0032479', 'Preimplantation lethality', 'XPO:0101450', 'abnormal myeloid cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(105669, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100799', 'abnormal genital ridge', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(105670, 'HP:0032479', 'Preimplantation lethality', 'XPO:0131667', 'abnormal actin cytoskeleton', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(105671, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100207', 'abnormal blastema', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105672, 'HP:0032479', 'Preimplantation lethality', 'XPO:0107278', 'abnormal medial region', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105673, 'HP:0032479', 'Preimplantation lethality', 'XPO:0141315', 'abnormal anatomical region', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105674, 'HP:0032479', 'Preimplantation lethality', 'XPO:0141892', 'abnormal inositol metabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(105675, 'HP:0032479', 'Preimplantation lethality', 'XPO:0101570', 'abnormal forelimb region', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105676, 'HP:0032479', 'Preimplantation lethality', 'XPO:0101396', 'abnormal apical epithelial cap', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105677, 'HP:0032479', 'Preimplantation lethality', 'XPO:0101543', 'abnormal external gill', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(105678, 'HP:0032479', 'Preimplantation lethality', 'XPO:0101057', 'abnormal vegetal pole', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105679, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100186', 'abnormal uveal tract', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105680, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100398', 'abnormal vegetal blastomere', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(105681, 'HP:0032479', 'Preimplantation lethality', 'XPO:0101740', 'abnormal cell part morphology', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(105682, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100093', 'abnormal simple squamous epithelium', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105683, 'HP:0032479', 'Preimplantation lethality', 'XPO:0101110', 'abnormal cell-free extract', 0.5294117647058824, 1.706362323152461, 0.9504568842024205, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105684, 'HP:0032479', 'Preimplantation lethality', 'XPO:0101074', 'abnormal germinal vesicle', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(105685, 'HP:0032479', 'Preimplantation lethality', 'XPO:0101461', 'abnormal sperm entry point', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(105686, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100985', 'abnormal simple columnar epithelium', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105687, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100846', 'abnormal hindlimb', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(105688, 'HP:0032479', 'Preimplantation lethality', 'XPO:0101023', 'abnormal ultimobranchial body', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(105689, 'HP:0032479', 'Preimplantation lethality', 'XPO:0141787', 'abnormal hormone metabolic process', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(105690, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100429', 'abnormal spermatid', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(105691, 'HP:0032479', 'Preimplantation lethality', 'XPO:0101099', 'abnormal ventro-lateral marginal zone', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105692, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100296', 'abnormal tail region', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105693, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100062', 'abnormal anatomical space', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105694, 'HP:0032479', 'Preimplantation lethality', 'XPO:0141745', 'abnormal creatinine homeostasis', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(105695, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100545', 'abnormal male organism', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105696, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100750', 'abnormal regenerating fin', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105697, 'HP:0032479', 'Preimplantation lethality', 'XPO:0101241', 'abnormal nucleate erythrocyte', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(105698, 'HP:0032479', 'Preimplantation lethality', 'XPO:0133403', 'abnormal developmental process', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(105699, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100417', 'abnormal dense regular connective tissue', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(105700, 'HP:0032479', 'Preimplantation lethality', 'XPO:0101078', 'abnormal mucous gland', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105701, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100533', 'abnormal melanoblast', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(105702, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100867', 'abnormal apical mesenchyme', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105703, 'HP:0032479', 'Preimplantation lethality', 'XPO:0141772', 'abnormal water homeostasis', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(105704, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100307', 'abnormal blastomere', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(105705, 'HP:0032479', 'Preimplantation lethality', 'XPO:0101500', 'abnormal endodermal cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(105706, 'HP:0032479', 'Preimplantation lethality', 'XPO:0141786', 'abnormal pigment metabolic process', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(105707, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100511', 'abnormal stylopod', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(105708, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100547', 'abnormal blastomere V2', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(105709, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100010', 'abnormal multicellular anatomical structure', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105710, 'HP:0032479', 'Preimplantation lethality', 'XPO:0141781', 'abnormal secondary metabolic process', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(105711, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100133', 'abnormal solid compound organ', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105712, 'HP:0032479', 'Preimplantation lethality', 'XPO:0141904', 'abnormal glucosamine metabolic process', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(105713, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100800', 'abnormal ventral marginal zone', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105714, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100852', 'abnormal interdigital region', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(105715, 'HP:0032479', 'Preimplantation lethality', 'XPO:0115362', 'abnormally decreased adhesivity of prechordal plate', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105716, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100344', 'abnormal portion of organism substance', 0.5625, 1.706362323152461, 0.9797085315405084, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105717, 'HP:0032479', 'Preimplantation lethality', 'XPO:0101518', 'abnormal B cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(105718, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100249', 'abnormal avascular GAG-rich matrix', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105719, 'HP:0032479', 'Preimplantation lethality', 'XPO:0101133', 'abnormal motor neuron', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(105720, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100383', 'abnormal amputated fin', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105721, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100228', 'abnormal skeletal subdivision', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(105722, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100484', 'abnormal cement gland primordium', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105723, 'HP:0032479', 'Preimplantation lethality', 'XPO:0101976', 'abnormal portion of organism substance morphology', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105724, 'HP:0032479', 'Preimplantation lethality', 'XPO:0141860', 'abnormal malate-aspartate shuttle', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(105725, 'HP:0032479', 'Preimplantation lethality', 'XPO:0107268', 'abnormal left side', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105726, 'HP:0032479', 'Preimplantation lethality', 'XPO:0107284', 'abnormal migrating myoblast', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(105727, 'HP:0032479', 'Preimplantation lethality', 'XPO:0101501', 'abnormal parabrachial area', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(105728, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100104', 'abnormal embryonic structure', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105729, 'HP:0032479', 'Preimplantation lethality', 'XPO:0101535', 'abnormal absorptive cell', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(105730, 'HP:0032479', 'Preimplantation lethality', 'XPO:0101228', 'abnormal mesenchymal stem cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(105731, 'HP:0032479', 'Preimplantation lethality', 'XPO:0141263', 'abnormal visually guided collision avoidance behavior', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(105732, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100976', 'abnormal multiciliated cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(105733, 'HP:0032479', 'Preimplantation lethality', 'XPO:0141797', 'abnormal hydrogen metabolic process', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(105734, 'HP:0032479', 'Preimplantation lethality', 'XPO:0101575', 'abnormal vitelline membrane', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(105735, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100384', 'abnormal amputated tissue', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105736, 'HP:0032479', 'Preimplantation lethality', 'XPO:0141777', 'abnormal catabolic process', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(105737, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100172', 'abnormal stem cell', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(105738, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100196', 'abnormal neuron', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(105739, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100727', 'abnormal odontogenic papilla', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(105740, 'HP:0032479', 'Preimplantation lethality', 'XPO:0101378', 'abnormal blastomere D1', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(105741, 'HP:0032479', 'Preimplantation lethality', 'XPO:0141715', 'abnormal septum', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105742, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100176', 'abnormal stage VI oocyte', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(105743, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100503', 'abnormal blastomere D2', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(105744, 'HP:0032479', 'Preimplantation lethality', 'XPO:0101162', 'abnormal stromal cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(105745, 'HP:0032479', 'Preimplantation lethality', 'XPO:0101503', 'abnormal organ cortex', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105746, 'HP:0032479', 'Preimplantation lethality', 'XPO:0126624', 'abnormally localised anatomical line', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105747, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100715', 'abnormal ciliated cell', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(105748, 'HP:0032479', 'Preimplantation lethality', 'XPO:0141600', 'absent metamorphosis', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(105749, 'HP:0032479', 'Preimplantation lethality', 'XPO:0131725', 'abnormal phosphorylation of RNA polymerase II C-terminal domain', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(105750, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100158', 'abnormal neuromere', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(105751, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100781', 'abnormal presumptive ectoderm', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105752, 'HP:0032479', 'Preimplantation lethality', 'XPO:0107273', 'abnormal basal region', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105753, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100242', 'abnormal right lymph heart', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(105754, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100225', 'abnormal endocrine system', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(105755, 'HP:0032479', 'Preimplantation lethality', 'XPO:0101098', 'abnormal mineralized extracellular matrix', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105756, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100256', 'abnormal paired appendage', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105757, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100913', 'abnormal Brachets cleft', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105758, 'HP:0032479', 'Preimplantation lethality', 'XPO:0101061', 'abnormal plasma membrane', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(105759, 'HP:0032479', 'Preimplantation lethality', 'XPO:0101553', 'abnormal dental epithelium', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105760, 'HP:0032479', 'Preimplantation lethality', 'XPO:0141264', 'abnormal schooling behavior', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(105761, 'HP:0032479', 'Preimplantation lethality', 'XPO:0101409', 'abnormal perivitelline space', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(105762, 'HP:0032479', 'Preimplantation lethality', 'XPO:0131469', 'abnormal heart process', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(105763, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100205', 'abnormal limb segment', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(105764, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100762', 'abnormal intersomitic region', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105765, 'HP:0032479', 'Preimplantation lethality', 'XPO:0101333', 'abnormal barrier epithelial cell', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(105766, 'HP:0032479', 'Preimplantation lethality', 'XPO:0116091', 'abnormally increased variability of size of cell in endoderm', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(105767, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100069', 'abnormal urinary system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(105768, 'HP:0032479', 'Preimplantation lethality', 'XPO:0141771', 'abnormal urea homeostasis', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(105769, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100691', 'abnormal keratin accumulating cell', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(105770, 'HP:0032479', 'Preimplantation lethality', 'XPO:0142054', 'abnormal digestive tract', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(105771, 'HP:0032479', 'Preimplantation lethality', 'XPO:0142052', 'abnormal nasal region', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(105772, 'HP:0032479', 'Preimplantation lethality', 'XPO:0101072', 'abnormal mitochondrial cloud', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(105773, 'HP:0032479', 'Preimplantation lethality', 'XPO:0101448', 'abnormal myelin accumulating cell', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(105774, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100734', 'abnormal lateral line system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(105775, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100626', 'abnormal primordial germ cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(105776, 'HP:0032479', 'Preimplantation lethality', 'XPO:0131675', 'abnormal spindle microtubule', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(105777, 'HP:0032479', 'Preimplantation lethality', 'XPO:0107263', 'abnormal anatomical side', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105778, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100864', 'abnormal dorsolateral ascending neuron', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(105779, 'HP:0032479', 'Preimplantation lethality', 'XPO:0141783', 'abnormal collagen metabolic process', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(105780, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100339', 'abnormal circumblastoporal collar', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105781, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100912', 'abnormal trabecula', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105782, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100289', 'abnormal chondroblast', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(105783, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100023', 'abnormal mesenchyme', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105784, 'HP:0032479', 'Preimplantation lethality', 'XPO:0141809', 'abnormal catalytic activity', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(105785, 'HP:0032479', 'Preimplantation lethality', 'XPO:0101263', 'abnormal blastocoel floor', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105786, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100704', 'abnormal Merkel cell', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(105787, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100890', 'abnormal pharyngeal cavity', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(105788, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100135', 'abnormal surface structure', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105789, 'HP:0032479', 'Preimplantation lethality', 'XPO:0101096', 'abnormal tendon', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(105790, 'HP:0032479', 'Preimplantation lethality', 'XPO:0101713', 'abnormal anatomical entity in vitro morphology', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105791, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100701', 'abnormal microglial cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(105792, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100146', 'abnormal primary germ layer', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105793, 'HP:0032479', 'Preimplantation lethality', 'XPO:0141790', 'abnormal cellular metabolic process', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(105794, 'HP:0032479', 'Preimplantation lethality', 'XPO:0101136', 'abnormal ooplasm', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(105795, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100894', 'abnormal nucleus', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(105796, 'HP:0032479', 'Preimplantation lethality', 'XPO:0101411', 'abnormal marginal zone (sensu neural)', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105797, 'HP:0032479', 'Preimplantation lethality', 'XPO:0101141', 'abnormal Keller explant', 0.5294117647058824, 1.706362323152461, 0.9504568842024205, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105798, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100002', 'abnormal head', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(105799, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100956', 'abnormal centrosome', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(105800, 'HP:0032479', 'Preimplantation lethality', 'XPO:0101451', 'abnormal dorsal lymph space', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(105801, 'HP:0032479', 'Preimplantation lethality', 'XPO:0101569', 'abnormal activin-induced ectoderm', 0.5294117647058824, 1.706362323152461, 0.9504568842024205, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105802, 'HP:0032479', 'Preimplantation lethality', 'XPO:0101092', 'abnormal dorso-lateral marginal zone', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105803, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100585', 'abnormal elastica externa', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(105804, 'HP:0032479', 'Preimplantation lethality', 'XPO:0141265', 'abnormal escape behavior', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(105805, 'HP:0032479', 'Preimplantation lethality', 'XPO:0107261', 'abnormal dorsal-ventral axis', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105806, 'HP:0032479', 'Preimplantation lethality', 'XPO:0101283', 'abnormal left-ventral blastomere', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(105807, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100202', 'abnormal embryo', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105808, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100745', 'abnormal anterior lymph sac', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(105809, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100726', 'abnormal tail', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105810, 'HP:0032479', 'Preimplantation lethality', 'XPO:0101174', 'abnormal articular system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(105811, 'HP:0032479', 'Preimplantation lethality', 'XPO:0131666', 'abnormal adherens junction', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(105812, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100735', 'abnormal hindgut', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(105813, 'HP:0032479', 'Preimplantation lethality', 'XPO:0124719', 'absent anatomical structure', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105814, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100081', 'abnormal anatomical entity in vitro', 0.5625, 1.706362323152461, 0.9797085315405084, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105815, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100393', 'abnormal involuting marginal zone', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105816, 'HP:0032479', 'Preimplantation lethality', 'XPO:0101366', 'abnormal morula cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(105817, 'HP:0032479', 'Preimplantation lethality', 'XPO:0101176', 'abnormal non-ciliated epithelial cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(105818, 'HP:0032479', 'Preimplantation lethality', 'XPO:0107276', 'abnormal dorsal region', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105819, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100784', 'abnormal left blastomere', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(105820, 'HP:0032479', 'Preimplantation lethality', 'XPO:0101498', 'abnormal stage II oocyte', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(105821, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100372', 'abnormal hematological system', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(105822, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100573', 'abnormal extraembryonic structure', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105823, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100823', 'abnormal blood', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(105824, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100201', 'abnormal cavitated compound organ', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105825, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100232', 'abnormal lymphatic system', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(105826, 'HP:0032479', 'Preimplantation lethality', 'XPO:0141272', 'absent surface breathing', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(105827, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100416', 'abnormal ligament', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(105828, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100261', 'abnormal multilaminar epithelium', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105829, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100728', 'abnormal cell condensation', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105830, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100557', 'abnormal prime meridian', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105831, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100687', 'abnormal periotic region', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(105832, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100915', 'abnormal dermal system', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105833, 'HP:0032479', 'Preimplantation lethality', 'XPO:0141798', 'abnormal lipid metabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(105834, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100616', 'abnormal ventral blood island', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(105835, 'HP:0032479', 'Preimplantation lethality', 'XPO:0102113', 'abnormal anatomical line morphology', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105836, 'HP:0032479', 'Preimplantation lethality', 'XPO:0141776', 'abnormal metabolic process', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(105837, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100394', 'abnormal marginal zone', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105838, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100899', 'abnormal secondary spermatogonium', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(105839, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100218', 'abnormal epithelial cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(105840, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100640', 'abnormal notochordal sheath', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(105841, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100444', 'abnormal cement gland', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105842, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100006', 'abnormal anatomical structure', 0.5625, 1.706362323152461, 0.9797085315405084, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105843, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100070', 'abnormal anatomical system', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105844, 'HP:0032479', 'Preimplantation lethality', 'XPO:0131691', 'abnormal molecular function', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(105845, 'HP:0032479', 'Preimplantation lethality', 'XPO:0141775', 'abnormal nitrogen compound metabolic process', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(105846, 'HP:0032479', 'Preimplantation lethality', 'XPO:0141738', 'abnormal carbon dioxide homeostasis', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(105847, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100760', 'abnormal Stirnorgan', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(105848, 'HP:0032479', 'Preimplantation lethality', 'XPO:0107311', 'abnormal apical junction complex', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(105849, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100816', 'abnormal blastocoel anlage', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105850, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100025', 'abnormal oocyte', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(105851, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100791', 'abnormal multiciliated cell precursor', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(105852, 'HP:0032479', 'Preimplantation lethality', 'XPO:0101132', 'abnormal apoptotic cell', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(105853, 'HP:0032479', 'Preimplantation lethality', 'XPO:0101200', 'abnormal joint region', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105854, 'HP:0032479', 'Preimplantation lethality', 'XPO:0107339', 'abnormal yolk platelet', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(105855, 'HP:0032479', 'Preimplantation lethality', 'XPO:0101083', 'abnormal T cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(105856, 'HP:0032479', 'Preimplantation lethality', 'XPO:0101212', 'abnormal glomeral mesenchyme', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(105857, 'HP:0032479', 'Preimplantation lethality', 'XPO:0107269', 'abnormal right side', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105858, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100192', 'abnormal epithelium', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105859, 'HP:0032479', 'Preimplantation lethality', 'XPO:0141748', 'abnormal gas homeostasis', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(105860, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100465', 'abnormal skeletal system', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(105861, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100907', 'abnormal cytoplasm', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(105862, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100707', 'abnormal central vegetal yolk mass', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105863, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100989', 'abnormal right blastomere', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(105864, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100267', 'abnormal wound epidermis', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105865, 'HP:0032479', 'Preimplantation lethality', 'XPO:0101168', 'abnormal circulating cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(105866, 'HP:0032479', 'Preimplantation lethality', 'XPO:0101029', 'abnormal right spleen primordium', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(105867, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100114', 'abnormal peripheral nervous system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(105868, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100156', 'abnormal foregut', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(105869, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100721', 'abnormal centromere', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(105870, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100627', 'abnormal pharyngeal region', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(105871, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100337', 'abnormal zygote', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(105872, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100059', 'abnormal regenerating tail', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105873, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100741', 'abnormal blastopore', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105874, 'HP:0032479', 'Preimplantation lethality', 'XPO:0101497', 'abnormal ciliary axoneme', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(105875, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100402', 'abnormal zeugopod', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(105876, 'HP:0032479', 'Preimplantation lethality', 'XPO:0101405', 'abnormal ring structure', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(105877, 'HP:0032479', 'Preimplantation lethality', 'XPO:0107253', 'abnormal enteric nervous system', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(105878, 'HP:0032479', 'Preimplantation lethality', 'XPO:0107259', 'abnormal animal-vegetal axis', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105879, 'HP:0032479', 'Preimplantation lethality', 'XPO:0141714', 'abnormal anterior notochord', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(105880, 'HP:0032479', 'Preimplantation lethality', 'XPO:0142051', 'abnormal cerebrospinal fluid', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(105881, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100540', 'abnormal left lymph heart', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(105882, 'HP:0032479', 'Preimplantation lethality', 'XPO:0141718', 'abnormal posterior notochord', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(105883, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100515', 'abnormal somatic stem cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(105884, 'HP:0032479', 'Preimplantation lethality', 'XPO:0101402', 'abnormal oropharyngeal papilla', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(105885, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100843', 'abnormal fasciculated network of fibrils', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(105886, 'HP:0032479', 'Preimplantation lethality', 'XPO:0101220', 'abnormal centriole', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(105887, 'HP:0032479', 'Preimplantation lethality', 'XPO:0131730', 'abnormal regulation of protein folding', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(105888, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100854', 'abnormal spiracle', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105889, 'HP:0032479', 'Preimplantation lethality', 'XPO:0101389', 'abnormal wedge region', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(105890, 'HP:0032479', 'Preimplantation lethality', 'XPO:0131687', 'abnormal astral microtubule', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(105891, 'HP:0032479', 'Preimplantation lethality', 'XPO:0101490', 'abnormal ectodermal cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(105892, 'HP:0032479', 'Preimplantation lethality', 'XPO:0101638', 'abnormal anatomical structure morphology', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105893, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100162', 'abnormal presumptive rhombomere', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105894, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100103', 'abnormal trunk', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105895, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100392', 'abnormal cilium', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(105896, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100268', 'abnormal circulatory system', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105897, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100969', 'abnormal disaggregated/reaggregated ectoderm treated with activin', 0.5294117647058824, 1.706362323152461, 0.9504568842024205, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105898, 'HP:0032479', 'Preimplantation lethality', 'XPO:0107266', 'abnormal dorsal side', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105899, 'HP:0032479', 'Preimplantation lethality', 'XPO:0101547', 'abnormal lampbrush chromosome', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(105900, 'HP:0032479', 'Preimplantation lethality', 'XPO:0101010', 'abnormal dorsal marginal zone', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105901, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100477', 'abnormal pericyte', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(105902, 'HP:0032479', 'Preimplantation lethality', 'XPO:0116494', 'absent biological process', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(105903, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100916', 'abnormal principal cavity', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(105904, 'HP:0032479', 'Preimplantation lethality', 'XPO:0131677', 'abnormal actin filament', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(105905, 'HP:0032479', 'Preimplantation lethality', 'XPO:0141499', 'abnormal tadpole', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105906, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100667', 'abnormal vegetal yolk mass', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105907, 'HP:0032479', 'Preimplantation lethality', 'XPO:0141770', 'abnormal urate homeostasis', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(105908, 'HP:0032479', 'Preimplantation lethality', 'XPO:0101472', 'abnormal zygote cortex', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(105909, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100724', 'abnormal kinetochore', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(105910, 'HP:0032479', 'Preimplantation lethality', 'XPO:00000000', 'Xenopus phenotype', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(105911, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100282', 'abnormal pelvic girdle primordium', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105912, 'HP:0032479', 'Preimplantation lethality', 'XPO:0116434', 'abnormal biological process', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(105913, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100274', 'abnormal sensory system', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(105914, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100827', 'abnormal atypical epithelium', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105915, 'HP:0032479', 'Preimplantation lethality', 'XPO:0101362', 'abnormal vegetal cortex', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(105916, 'HP:0032479', 'Preimplantation lethality', 'XPO:0131745', 'abnormal axis elongation', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(105917, 'HP:0032479', 'Preimplantation lethality', 'XPO:0101573', 'abnormal peripheral vegetal yolk mass', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105918, 'HP:0032479', 'Preimplantation lethality', 'XPO:0115508', 'abnormally peramorphic growth of whole organism', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105919, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100386', 'abnormal limb', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(105920, 'HP:0032479', 'Preimplantation lethality', 'XPO:0141794', 'abnormal prosthetic group metabolic process', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(105921, 'HP:0032479', 'Preimplantation lethality', 'XPO:0107272', 'abnormal axial region', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(105922, 'HP:0032479', 'Preimplantation lethality', 'XPO:0126318', 'abnormally localised cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(105923, 'HP:0032479', 'Preimplantation lethality', 'XPO:0100754', 'abnormal electrically active cell', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(105924, 'HP:0011078', 'Abnormality of canine', 'XPO:0101567', 'abnormal tongue', 0.6530612244897959, 7.884497199543557, 2.269153894212616, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(105925, 'HP:0011078', 'Abnormality of canine', 'XPO:0129585', 'increased size of the tongue', 0.44, 7.884497199543557, 1.8625731577039237, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(105926, 'HP:0011078', 'Abnormality of canine', 'XPO:0127611', 'abnormally localised lower jaw', 0.4262295081967213, 7.0866363731414825, 1.737968220679852, 'HP:0000153', 'Abnormality of the mouth'),
(105927, 'HP:0011078', 'Abnormality of canine', 'XPO:0128880', 'decreased size of the lower jaw', 0.42857142857142855, 7.312692920701687, 1.7703138850862843, 'UPHENO:0076800', 'abnormal mouth morphology'),
(105928, 'HP:0011078', 'Abnormality of canine', 'XPO:0140639', 'abnormally necrotic upper jaw', 0.42857142857142855, 7.312692920701687, 1.7703138850862843, 'UPHENO:0076800', 'abnormal mouth morphology'),
(105929, 'HP:0011078', 'Abnormality of canine', 'XPO:0103138', 'abnormal upper jaw morphology', 0.4583333333333333, 7.312692920701687, 1.830751463740579, 'UPHENO:0076800', 'abnormal mouth morphology'),
(105930, 'HP:0011078', 'Abnormality of canine', 'XPO:0129152', 'decreased size of the oral cavity', 0.5079365079365079, 7.884497199543557, 2.0012056302067838, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(105931, 'HP:0011078', 'Abnormality of canine', 'XPO:0102890', 'abnormal dentine morphology', 0.4457831325301205, 9.181382707377857, 2.0230930636658266, 'UPHENO:0002826', 'abnormal dentition'),
(105932, 'HP:0011078', 'Abnormality of canine', 'XPO:0127750', 'abnormally localised tongue', 0.5333333333333333, 7.884497199543557, 2.0506255565290066, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(105933, 'HP:0011078', 'Abnormality of canine', 'XPO:0139736', 'abnormally necrotic tooth', 0.4625, 9.181382707377857, 2.060676952402355, 'UPHENO:0002826', 'abnormal dentition'),
(105934, 'HP:0011078', 'Abnormality of canine', 'XPO:0140897', 'abnormally necrotic lower jaw', 0.44, 7.312692920701687, 1.7937627728071353, 'UPHENO:0076800', 'abnormal mouth morphology'),
(105935, 'HP:0011078', 'Abnormality of canine', 'XPO:0140890', 'abnormally necrotic dentine', 0.40217391304347827, 9.181382707377857, 1.9215911663451926, 'UPHENO:0002826', 'abnormal dentition'),
(105936, 'HP:0011078', 'Abnormality of canine', 'XPO:0128105', 'decreased size of the tongue', 0.4507042253521127, 7.884497199543557, 1.885093154889482, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(105937, 'HP:0011078', 'Abnormality of canine', 'XPO:0102960', 'abnormal oral epithelium morphology', 0.44776119402985076, 7.312692920701687, 1.8095137782694621, 'UPHENO:0076800', 'abnormal mouth morphology'),
(105938, 'HP:0011078', 'Abnormality of canine', 'XPO:0100027', 'abnormal lower jaw', 0.5, 7.0866363731414825, 1.8823703638154583, 'HP:0000153', 'Abnormality of the mouth'),
(105939, 'HP:0011078', 'Abnormality of canine', 'XPO:0103828', 'decreased width of the mouth', 0.4444444444444444, 7.884497199543557, 1.8719564571792031, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(105940, 'HP:0011078', 'Abnormality of canine', 'XPO:0115393', 'abnormally decreased volume of oral cavity', 0.49230769230769234, 7.884497199543557, 1.970177307075115, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(105941, 'HP:0011078', 'Abnormality of canine', 'XPO:0141311', 'abnormal roof of mouth morphology', 0.4918032786885246, 7.312692920701687, 1.8964193508935339, 'UPHENO:0076800', 'abnormal mouth morphology'),
(105942, 'HP:0011078', 'Abnormality of canine', 'XPO:0141830', 'increased width of mouth', 0.4444444444444444, 7.884497199543557, 1.8719564571792031, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(105943, 'HP:0011078', 'Abnormality of canine', 'XPO:0100184', 'abnormal tooth', 0.45614035087719296, 7.0866363731414825, 1.7979156826124616, 'HP:0000153', 'Abnormality of the mouth'),
(105944, 'HP:0011078', 'Abnormality of canine', 'XPO:0129990', 'increased size of the cementum', 0.4065934065934066, 9.181382707377857, 1.9321205118290519, 'UPHENO:0002826', 'abnormal dentition'),
(105945, 'HP:0011078', 'Abnormality of canine', 'XPO:0128510', 'decreased size of the cementum', 0.4065934065934066, 9.181382707377857, 1.9321205118290519, 'UPHENO:0002826', 'abnormal dentition'),
(105946, 'HP:0011078', 'Abnormality of canine', 'XPO:0103096', 'abnormal oral cavity morphology', 0.5517241379310345, 7.884497199543557, 2.0856815242116484, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(105947, 'HP:0011078', 'Abnormality of canine', 'XPO:0101506', 'abnormal upper jaw', 0.5, 7.0866363731414825, 1.8823703638154583, 'HP:0000153', 'Abnormality of the mouth'),
(105948, 'HP:0011078', 'Abnormality of canine', 'XPO:0130701', 'increased size of the upper jaw', 0.4177215189873418, 7.312692920701687, 1.7477611949930372, 'UPHENO:0076800', 'abnormal mouth morphology'),
(105949, 'HP:0011078', 'Abnormality of canine', 'XPO:0115558', 'abnormally incomplete structure of mouth', 0.5084745762711864, 7.312692920701687, 1.9282941773119304, 'UPHENO:0076800', 'abnormal mouth morphology'),
(105950, 'HP:0011078', 'Abnormality of canine', 'XPO:0101464', 'abnormal oral cavity', 0.4339622641509434, 7.0866363731414825, 1.7536626715827954, 'HP:0000153', 'Abnormality of the mouth'),
(105951, 'HP:0011078', 'Abnormality of canine', 'XPO:0101659', 'abnormal lower jaw morphology', 0.4714285714285714, 7.312692920701687, 1.856720866716972, 'UPHENO:0076800', 'abnormal mouth morphology'),
(105952, 'HP:0011078', 'Abnormality of canine', 'XPO:0100766', 'abnormal Meckels cartilage', 0.4126984126984127, 7.0866363731414825, 1.7101589348848036, 'HP:0000153', 'Abnormality of the mouth'),
(105953, 'HP:0011078', 'Abnormality of canine', 'XPO:0103199', 'abnormal tongue morphology', 0.5517241379310345, 7.884497199543557, 2.0856815242116484, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(105954, 'HP:0011078', 'Abnormality of canine', 'XPO:0127103', 'abnormally localised upper jaw', 0.4262295081967213, 7.0866363731414825, 1.737968220679852, 'HP:0000153', 'Abnormality of the mouth'),
(105955, 'HP:0011078', 'Abnormality of canine', 'XPO:0128989', 'decreased size of the tooth', 0.44047619047619047, 9.181382707377857, 2.0110147881728198, 'UPHENO:0002826', 'abnormal dentition'),
(105956, 'HP:0011078', 'Abnormality of canine', 'XPO:0131573', 'decreased size of the roof of mouth', 0.4411764705882353, 7.312692920701687, 1.7961592505261732, 'UPHENO:0076800', 'abnormal mouth morphology'),
(105957, 'HP:0011078', 'Abnormality of canine', 'XPO:0131651', 'abnormal roof of mouth', 0.42592592592592593, 7.0866363731414825, 1.7373491758799184, 'HP:0000153', 'Abnormality of the mouth'),
(105958, 'HP:0011078', 'Abnormality of canine', 'XPO:0140789', 'abnormally necrotic roof of mouth', 0.45454545454545453, 7.312692920701687, 1.8231706797751206, 'UPHENO:0076800', 'abnormal mouth morphology'),
(105959, 'HP:0011078', 'Abnormality of canine', 'XPO:0131611', 'increased size of the roof of mouth', 0.4411764705882353, 7.312692920701687, 1.7961592505261732, 'UPHENO:0076800', 'abnormal mouth morphology'),
(105960, 'HP:0011078', 'Abnormality of canine', 'XPO:0141006', 'abnormally necrotic cementum', 0.4157303370786517, 9.181382707377857, 1.9537091205669026, 'UPHENO:0002826', 'abnormal dentition'),
(105961, 'HP:0011078', 'Abnormality of canine', 'XPO:0140626', 'abnormally necrotic tongue', 0.5079365079365079, 7.884497199543557, 2.0012056302067838, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(105962, 'HP:0011078', 'Abnormality of canine', 'XPO:0103735', 'increased size of the mouth', 0.47761194029850745, 7.884497199543557, 1.9405488929043109, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(105963, 'HP:0011078', 'Abnormality of canine', 'XPO:0129225', 'decreased size of the upper jaw', 0.4177215189873418, 7.312692920701687, 1.7477611949930372, 'UPHENO:0076800', 'abnormal mouth morphology'),
(105964, 'HP:0011078', 'Abnormality of canine', 'XPO:0130466', 'increased size of the tooth', 0.44047619047619047, 9.181382707377857, 2.0110147881728198, 'UPHENO:0002826', 'abnormal dentition'),
(105965, 'HP:0011078', 'Abnormality of canine', 'XPO:0102861', 'abnormal cementum morphology', 0.4567901234567901, 9.181382707377857, 2.0479172201061178, 'UPHENO:0002826', 'abnormal dentition'),
(105966, 'HP:0011078', 'Abnormality of canine', 'XPO:0141009', 'abnormally necrotic oral epithelium', 0.40540540540540543, 7.312692920701687, 1.7218029033900208, 'UPHENO:0076800', 'abnormal mouth morphology'),
(105967, 'HP:0011078', 'Abnormality of canine', 'XPO:0100647', 'abnormal mouth', 0.4423076923076923, 7.0866363731414825, 1.7704445149249843, 'HP:0000153', 'Abnormality of the mouth'),
(105968, 'HP:0011078', 'Abnormality of canine', 'XPO:0126089', 'absent tongue', 0.5161290322580645, 7.884497199543557, 2.017279829235854, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(105969, 'HP:0011078', 'Abnormality of canine', 'XPO:0130628', 'increased size of the oral cavity', 0.5079365079365079, 7.884497199543557, 2.0012056302067838, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(105970, 'HP:0011078', 'Abnormality of canine', 'XPO:0102279', 'abnormal mouth morphology', 0.5172413793103449, 7.312692920701687, 1.9448463622550587, 'UPHENO:0076800', 'abnormal mouth morphology'),
(105971, 'HP:0011078', 'Abnormality of canine', 'XPO:0130358', 'increased size of the lower jaw', 0.42857142857142855, 7.312692920701687, 1.7703138850862843, 'UPHENO:0076800', 'abnormal mouth morphology'),
(105972, 'HP:0011078', 'Abnormality of canine', 'XPO:0103352', 'decreased size of the mouth', 0.47761194029850745, 7.884497199543557, 1.9405488929043109, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(105973, 'HP:0011078', 'Abnormality of canine', 'XPO:0102223', 'abnormal pharyngeal arch morphology', 0.41379310344827586, 5.725717590856133, 1.5392408685416148, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(105974, 'HP:0011078', 'Abnormality of canine', 'XPO:0101816', 'abnormal tooth morphology', 0.5138888888888888, 9.181382707377857, 2.172144230468609, 'UPHENO:0002826', 'abnormal dentition'),
(105975, 'HP:0011078', 'Abnormality of canine', 'XPO:0126046', 'absent tooth', 0.44047619047619047, 9.181382707377857, 2.0110147881728198, 'UPHENO:0002826', 'abnormal dentition'),
(105976, 'HP:0011078', 'Abnormality of canine', 'XPO:0101328', 'abnormal oral epithelium', 0.4107142857142857, 7.0866363731414825, 1.7060430229369012, 'HP:0000153', 'Abnormality of the mouth'),
(105977, 'HP:0033423', 'Pulmonary arterial hypertension with positive acute response to NO challenge', 'XPO:0101949', 'abnormal respiratory system morphology', 0.4067796610169492, 7.241224942262181, 1.7162700916117157, 'HP:0012252', 'Abnormal respiratory system morphology'),
(105978, 'HP:0033423', 'Pulmonary arterial hypertension with positive acute response to NO challenge', 'XPO:0127602', 'abnormally localised pulmonary artery', 0.4605263157894737, 12.257853533237922, 2.3759343692848596, 'HP:0004414', 'Abnormality of the pulmonary artery'),
(105979, 'HP:0033423', 'Pulmonary arterial hypertension with positive acute response to NO challenge', 'XPO:0126220', 'absent pulmonary vein', 0.4125, 11.341685124041394, 2.162971362193008, 'UPHENO:0002960', 'abnormal lung vasculature'),
(105980, 'HP:0033423', 'Pulmonary arterial hypertension with positive acute response to NO challenge', 'XPO:0100210', 'abnormal pulmonary artery', 0.5303030303030303, 12.257853533237922, 2.5495836667359586, 'HP:0004414', 'Abnormality of the pulmonary artery'),
(105981, 'HP:0033423', 'Pulmonary arterial hypertension with positive acute response to NO challenge', 'XPO:0127882', 'abnormally localised pulmonary vein', 0.4230769230769231, 11.341685124041394, 2.190526248367443, 'UPHENO:0002960', 'abnormal lung vasculature'),
(105982, 'HP:0033423', 'Pulmonary arterial hypertension with positive acute response to NO challenge', 'XPO:0101842', 'abnormal pulmonary artery morphology', 0.4166666666666667, 12.257853533237922, 2.259964374095855, 'HP:0004414', 'Abnormality of the pulmonary artery'),
(105983, 'HP:0033423', 'Pulmonary arterial hypertension with positive acute response to NO challenge', 'XPO:0101548', 'abnormal pulmonary vein', 0.4852941176470588, 11.341685124041394, 2.3460718392458575, 'UPHENO:0002960', 'abnormal lung vasculature'),
(105984, 'HP:0031548', 'Follicular infundibulum tumor', 'XPO:0140144', 'abnormally necrotic portion of organism substance', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(105985, 'HP:0031548', 'Follicular infundibulum tumor', 'XPO:0102561', 'abnormal dermis morphology', 0.41304347826086957, 6.8660902472206855, 1.6840409133287308, 'HP:0000951', 'Abnormality of the skin'),
(105986, 'HP:0031548', 'Follicular infundibulum tumor', 'XPO:0115392', 'abnormally incomplete structure of alimentary system', 0.40476190476190477, 4.970960464763942, 1.4184693955859522, 'HP:0011793', 'Neoplasm by anatomical site'),
(105987, 'HP:0031548', 'Follicular infundibulum tumor', 'XPO:0101638', 'abnormal anatomical structure morphology', 0.43333333333333335, 2.786899518863159, 1.0989342374200721, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(105988, 'HP:0031548', 'Follicular infundibulum tumor', 'XPO:0107345', 'abnormal anatomical axis morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(105989, 'HP:0031548', 'Follicular infundibulum tumor', 'XPO:0100507', 'abnormal skin', 0.40540540540540543, 6.8660902472206855, 1.6683974647021622, 'HP:0000951', 'Abnormality of the skin'),
(105990, 'HP:0031548', 'Follicular infundibulum tumor', 'XPO:0102727', 'abnormal skin seromucous gland morphology', 0.40425531914893614, 6.8660902472206855, 1.6660292627068698, 'HP:0000951', 'Abnormality of the skin'),
(105991, 'HP:0031548', 'Follicular infundibulum tumor', 'XPO:0102139', 'abnormal skin morphology', 0.4222222222222222, 6.8660902472206855, 1.7026496651278105, 'HP:0000951', 'Abnormality of the skin'),
(105992, 'HP:0031548', 'Follicular infundibulum tumor', 'XPO:0103201', 'abnormal activin-induced ectoderm morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(105993, 'HP:0031548', 'Follicular infundibulum tumor', 'XPO:0102742', 'abnormal cell-free extract morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(105994, 'HP:0031548', 'Follicular infundibulum tumor', 'XPO:0102773', 'abnormal Keller explant morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(105995, 'HP:0031548', 'Follicular infundibulum tumor', 'XPO:0101713', 'abnormal anatomical entity in vitro morphology', 0.43333333333333335, 2.786899518863159, 1.0989342374200721, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(105996, 'HP:0031548', 'Follicular infundibulum tumor', 'XPO:0101784', 'abnormal alimentary system morphology', 0.4146341463414634, 4.970960464763942, 1.4356635917945963, 'HP:0011793', 'Neoplasm by anatomical site'),
(105997, 'HP:0031548', 'Follicular infundibulum tumor', 'XPO:0140269', 'abnormally necrotic anatomical line', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(105998, 'HP:0031548', 'Follicular infundibulum tumor', 'XPO:0102615', 'abnormal skin gland morphology', 0.4222222222222222, 6.8660902472206855, 1.7026496651278105, 'HP:0000951', 'Abnormality of the skin'),
(105999, 'HP:0031548', 'Follicular infundibulum tumor', 'XPO:0101636', 'abnormal cell morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(106000, 'HP:0031548', 'Follicular infundibulum tumor', 'XPO:0102178', 'abnormal whole organism morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(106001, 'HP:0031548', 'Follicular infundibulum tumor', 'XPO:0101890', 'abnormal organ part morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(106002, 'HP:0031548', 'Follicular infundibulum tumor', 'XPO:0101694', 'abnormal anatomical space morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(106003, 'HP:0031548', 'Follicular infundibulum tumor', 'XPO:0141316', 'abnormal anatomical region morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(106004, 'HP:0031548', 'Follicular infundibulum tumor', 'XPO:0139718', 'abnormally necrotic anatomical structure', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(106005, 'HP:0031548', 'Follicular infundibulum tumor', 'XPO:0102601', 'abnormal disaggregated/reaggregated ectoderm treated with activin morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(106006, 'HP:0031548', 'Follicular infundibulum tumor', 'XPO:0101740', 'abnormal cell part morphology', 0.4166666666666667, 2.786899518863159, 1.0775936770692605, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(106007, 'HP:0031548', 'Follicular infundibulum tumor', 'XPO:0102626', 'abnormal granular gland morphology', 0.40425531914893614, 6.8660902472206855, 1.6660292627068698, 'HP:0000951', 'Abnormality of the skin'),
(106008, 'HP:0031548', 'Follicular infundibulum tumor', 'XPO:0101976', 'abnormal portion of organism substance morphology', 0.43333333333333335, 2.786899518863159, 1.0989342374200721, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(106009, 'HP:0031548', 'Follicular infundibulum tumor', 'XPO:0102522', 'abnormal pharyngeal cavity morphology', 0.4146341463414634, 4.970960464763942, 1.4356635917945963, 'HP:0011793', 'Neoplasm by anatomical site'),
(106010, 'HP:0031548', 'Follicular infundibulum tumor', 'XPO:0102113', 'abnormal anatomical line morphology', 0.43333333333333335, 2.786899518863159, 1.0989342374200721, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(106011, 'HP:0025465', 'Abnormal circulating beta globulin level', 'XPO:0141873', 'abnormal tricarboxylic acid metabolic process', 0.42592592592592593, 7.41682187759612, 1.7773622944247445, 'HP:0430071', 'Abnormal circulating organic compound concentration'),
(106012, 'HP:0025598', 'Inferior oblique muscle weakness', 'XPO:0101554', 'abnormal peripheral retina', 0.4117647058823529, 6.02624522851634, 1.5752444553449358, 'HP:0000478', 'Abnormality of the eye'),
(106013, 'HP:0025598', 'Inferior oblique muscle weakness', 'XPO:0101173', 'abnormal retinal layer', 0.45652173913043476, 6.02624522851634, 1.6586476274811248, 'HP:0000478', 'Abnormality of the eye'),
(106014, 'HP:0025598', 'Inferior oblique muscle weakness', 'XPO:0142052', 'abnormal nasal region', 0.40540540540540543, 3.868794716113063, 1.2523698696136485, 'UPHENO:0002844', 'abnormal head'),
(106015, 'HP:0025598', 'Inferior oblique muscle weakness', 'XPO:0100881', 'abnormal sclera', 0.42, 6.02624522851634, 1.590918915588366, 'HP:0000478', 'Abnormality of the eye'),
(106016, 'HP:0025598', 'Inferior oblique muscle weakness', 'XPO:0101289', 'abnormal orbital region', 0.40425531914893614, 5.757493499662858, 1.5256137690136826, 'HP:0000315', 'Abnormality of the orbital region'),
(106017, 'HP:0025598', 'Inferior oblique muscle weakness', 'XPO:0101230', 'abnormal iris', 0.40384615384615385, 6.02624522851634, 1.560024345217106, 'HP:0000478', 'Abnormality of the eye'),
(106018, 'HP:0025598', 'Inferior oblique muscle weakness', 'XPO:0100002', 'abnormal head', 0.40540540540540543, 3.868794716113063, 1.2523698696136485, 'UPHENO:0002844', 'abnormal head'),
(106019, 'HP:0025598', 'Inferior oblique muscle weakness', 'XPO:0100564', 'abnormal central retina', 0.4117647058823529, 6.02624522851634, 1.5752444553449358, 'HP:0000478', 'Abnormality of the eye'),
(106020, 'HP:0025598', 'Inferior oblique muscle weakness', 'XPO:0101578', 'abnormal pupil', 0.4117647058823529, 6.02624522851634, 1.5752444553449358, 'HP:0000478', 'Abnormality of the eye'),
(106021, 'HP:0025598', 'Inferior oblique muscle weakness', 'XPO:0100844', 'abnormal lens transitional zone', 0.40384615384615385, 6.02624522851634, 1.560024345217106, 'HP:0000478', 'Abnormality of the eye'),
(106022, 'HP:0025598', 'Inferior oblique muscle weakness', 'XPO:0101390', 'abnormal ciliary body', 0.40384615384615385, 6.02624522851634, 1.560024345217106, 'HP:0000478', 'Abnormality of the eye'),
(106023, 'HP:0025598', 'Inferior oblique muscle weakness', 'XPO:0101416', 'abnormal cornea', 0.4117647058823529, 6.02624522851634, 1.5752444553449358, 'HP:0000478', 'Abnormality of the eye'),
(106024, 'HP:0025598', 'Inferior oblique muscle weakness', 'XPO:0100485', 'abnormal retina', 0.42, 6.02624522851634, 1.590918915588366, 'HP:0000478', 'Abnormality of the eye'),
(106025, 'HP:0025598', 'Inferior oblique muscle weakness', 'XPO:0100918', 'abnormal lens', 0.42, 6.02624522851634, 1.590918915588366, 'HP:0000478', 'Abnormality of the eye'),
(106026, 'HP:0030950', 'Pulmonary venous hypertension', 'XPO:0101583', 'abnormal truncus arteriosus', 0.41025641025641024, 5.809304221129108, 1.5437954190396599, 'UPHENO:0002678', 'abnormal vasculature'),
(106027, 'HP:0030950', 'Pulmonary venous hypertension', 'XPO:0100043', 'abnormal vein', 0.41025641025641024, 5.809304221129108, 1.5437954190396599, 'UPHENO:0002678', 'abnormal vasculature'),
(106028, 'HP:0030950', 'Pulmonary venous hypertension', 'XPO:0100981', 'abnormal dorsal longitudinal anastomosing vessel', 0.41025641025641024, 5.809304221129108, 1.5437954190396599, 'UPHENO:0002678', 'abnormal vasculature'),
(106029, 'HP:0030950', 'Pulmonary venous hypertension', 'XPO:0100054', 'abnormal blood vessel', 0.42105263157894735, 5.809304221129108, 1.5639766078650594, 'UPHENO:0002678', 'abnormal vasculature'),
(106030, 'HP:0030950', 'Pulmonary venous hypertension', 'XPO:0100076', 'abnormal artery', 0.41025641025641024, 5.809304221129108, 1.5437954190396599, 'UPHENO:0002678', 'abnormal vasculature'),
(106031, 'HP:0030950', 'Pulmonary venous hypertension', 'XPO:0101949', 'abnormal respiratory system morphology', 0.4090909090909091, 7.032762738978795, 1.6961837466234333, 'HP:0002795', 'Abnormal respiratory system physiology'),
(106032, 'HP:0030950', 'Pulmonary venous hypertension', 'XPO:0100792', 'abnormal capillary', 0.41025641025641024, 5.809304221129108, 1.5437954190396599, 'UPHENO:0002678', 'abnormal vasculature'),
(106033, 'HP:0030950', 'Pulmonary venous hypertension', 'XPO:0100780', 'abnormal vascular plexus', 0.41025641025641024, 5.809304221129108, 1.5437954190396599, 'UPHENO:0002678', 'abnormal vasculature'),
(106034, 'HP:0034638', 'Colonic fibrinopurulent exudate', 'XPO:0102920', 'abnormal external coil of the small intestine morphology', 0.41379310344827586, 8.518562886125473, 1.8774777158648677, 'UPHENO:0076783', 'abnormal intestine morphology'),
(106035, 'HP:0034638', 'Colonic fibrinopurulent exudate', 'XPO:0115766', 'abnormally inverted external coil of the small intestine', 0.4067796610169492, 8.518562886125473, 1.8614988915306085, 'UPHENO:0076783', 'abnormal intestine morphology'),
(106036, 'HP:0034638', 'Colonic fibrinopurulent exudate', 'XPO:0141833', 'edematous alimentary system', 0.42857142857142855, 5.725717590856133, 1.5664861849086864, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(106037, 'HP:0034638', 'Colonic fibrinopurulent exudate', 'XPO:0102522', 'abnormal pharyngeal cavity morphology', 0.45, 5.725717590856133, 1.6051706812315194, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(106038, 'HP:0034638', 'Colonic fibrinopurulent exudate', 'XPO:0102156', 'abnormal intestine morphology', 0.41379310344827586, 8.518562886125473, 1.8774777158648677, 'UPHENO:0076783', 'abnormal intestine morphology'),
(106039, 'HP:0034638', 'Colonic fibrinopurulent exudate', 'XPO:0102125', 'abnormal liver and biliary system morphology', 0.42857142857142855, 5.725717590856133, 1.5664861849086864, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(106040, 'HP:0034638', 'Colonic fibrinopurulent exudate', 'XPO:0101377', 'abnormal manicotto glandulare', 0.4166666666666667, 5.05060299610679, 1.45066119926208, 'HP:0025031', 'Abnormality of the digestive system'),
(106041, 'HP:0034638', 'Colonic fibrinopurulent exudate', 'XPO:0127665', 'abnormally localised duodenum', 0.4067796610169492, 8.518562886125473, 1.8614988915306085, 'UPHENO:0076783', 'abnormal intestine morphology'),
(106042, 'HP:0034638', 'Colonic fibrinopurulent exudate', 'XPO:0101288', 'abnormal external coil of the small intestine', 0.4897959183673469, 8.518562886125473, 2.042634899334637, 'UPHENO:0076783', 'abnormal intestine morphology'),
(106043, 'HP:0034638', 'Colonic fibrinopurulent exudate', 'XPO:0102367', 'abnormal hindgut morphology', 0.4090909090909091, 5.725717590856133, 1.5304701939081158, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(106044, 'HP:0034638', 'Colonic fibrinopurulent exudate', 'XPO:0107294', 'abnormal intestinal stem cell', 0.4528301886792453, 8.518562886125473, 1.9640423719971558, 'UPHENO:0076783', 'abnormal intestine morphology'),
(106045, 'HP:0034638', 'Colonic fibrinopurulent exudate', 'XPO:0142054', 'abnormal digestive tract', 0.42857142857142855, 5.05060299610679, 1.471238981671103, 'HP:0025031', 'Abnormality of the digestive system'),
(106046, 'HP:0034638', 'Colonic fibrinopurulent exudate', 'XPO:0127034', 'abnormally localised rectum', 0.4406779661016949, 10.665155383737162, 2.1679250408314017, 'HP:0002250', 'Abnormal large intestine morphology'),
(106047, 'HP:0034638', 'Colonic fibrinopurulent exudate', 'XPO:0101381', 'abnormal ventral foregut', 0.40540540540540543, 5.05060299610679, 1.4309233924911664, 'HP:0025031', 'Abnormality of the digestive system'),
(106048, 'HP:0034638', 'Colonic fibrinopurulent exudate', 'XPO:0142061', 'abnormal digestive tract morphology', 0.42857142857142855, 5.725717590856133, 1.5664861849086864, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(106049, 'HP:0034638', 'Colonic fibrinopurulent exudate', 'XPO:0101021', 'abnormal dorsal foregut', 0.40540540540540543, 5.05060299610679, 1.4309233924911664, 'HP:0025031', 'Abnormality of the digestive system'),
(106050, 'HP:0034638', 'Colonic fibrinopurulent exudate', 'XPO:0107375', 'abnormal larval alimentary system morphology', 0.42857142857142855, 5.725717590856133, 1.5664861849086864, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(106051, 'HP:0034638', 'Colonic fibrinopurulent exudate', 'XPO:0101321', 'abnormal duodenum', 0.4897959183673469, 8.518562886125473, 2.042634899334637, 'UPHENO:0076783', 'abnormal intestine morphology'),
(106052, 'HP:0034638', 'Colonic fibrinopurulent exudate', 'XPO:0100152', 'abnormal alimentary system', 0.45454545454545453, 5.05060299610679, 1.5151662069205463, 'HP:0025031', 'Abnormality of the digestive system'),
(106053, 'HP:0034638', 'Colonic fibrinopurulent exudate', 'XPO:0103169', 'abnormal internal coil of the small intestine morphology', 0.41379310344827586, 8.518562886125473, 1.8774777158648677, 'UPHENO:0076783', 'abnormal intestine morphology'),
(106054, 'HP:0034638', 'Colonic fibrinopurulent exudate', 'XPO:0126463', 'abnormally localised internal coil of the small intestine', 0.41379310344827586, 8.518562886125473, 1.8774777158648677, 'UPHENO:0076783', 'abnormal intestine morphology'),
(106055, 'HP:0034638', 'Colonic fibrinopurulent exudate', 'XPO:0139726', 'abnormally necrotic colon', 0.41935483870967744, 10.665155383737162, 2.1148249373791543, 'HP:0002250', 'Abnormal large intestine morphology'),
(106056, 'HP:0034638', 'Colonic fibrinopurulent exudate', 'XPO:0100735', 'abnormal hindgut', 0.4166666666666667, 5.05060299610679, 1.45066119926208, 'HP:0025031', 'Abnormality of the digestive system'),
(106057, 'HP:0034638', 'Colonic fibrinopurulent exudate', 'XPO:0100486', 'abnormal oral evagination', 0.4166666666666667, 5.05060299610679, 1.45066119926208, 'HP:0025031', 'Abnormality of the digestive system'),
(106058, 'HP:0034638', 'Colonic fibrinopurulent exudate', 'XPO:0100890', 'abnormal pharyngeal cavity', 0.42857142857142855, 5.05060299610679, 1.471238981671103, 'HP:0025031', 'Abnormality of the digestive system'),
(106059, 'HP:0034638', 'Colonic fibrinopurulent exudate', 'XPO:0103009', 'abnormal manicotto glandulare morphology', 0.4186046511627907, 5.725717590856133, 1.5481640787645816, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(106060, 'HP:0034638', 'Colonic fibrinopurulent exudate', 'XPO:0129624', 'increased size of the large intestine', 0.4262295081967213, 10.665155383737162, 2.1320891008707643, 'HP:0002250', 'Abnormal large intestine morphology'),
(106061, 'HP:0034638', 'Colonic fibrinopurulent exudate', 'XPO:0100523', 'abnormal midgut', 0.4166666666666667, 5.05060299610679, 1.45066119926208, 'HP:0025031', 'Abnormality of the digestive system'),
(106062, 'HP:0034638', 'Colonic fibrinopurulent exudate', 'XPO:0125399', 'absent rectum', 0.4126984126984127, 10.665155383737162, 2.0979734741054896, 'HP:0002250', 'Abnormal large intestine morphology'),
(106063, 'HP:0034638', 'Colonic fibrinopurulent exudate', 'XPO:0115392', 'abnormally incomplete structure of alimentary system', 0.43902439024390244, 5.725717590856133, 1.5854745895265556, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(106064, 'HP:0034638', 'Colonic fibrinopurulent exudate', 'XPO:0100361', 'abnormal small intestine', 0.5, 8.518562886125473, 2.0638026657272097, 'UPHENO:0076783', 'abnormal intestine morphology'),
(106065, 'HP:0034638', 'Colonic fibrinopurulent exudate', 'XPO:0127587', 'abnormally localised external coil of the small intestine', 0.41379310344827586, 8.518562886125473, 1.8774777158648677, 'UPHENO:0076783', 'abnormal intestine morphology'),
(106066, 'HP:0034638', 'Colonic fibrinopurulent exudate', 'XPO:0141240', 'abnormally necrotic rectum', 0.40625, 10.665155383737162, 2.081518526135, 'HP:0002250', 'Abnormal large intestine morphology'),
(106067, 'HP:0034638', 'Colonic fibrinopurulent exudate', 'XPO:0101784', 'abnormal alimentary system morphology', 0.45, 5.725717590856133, 1.6051706812315194, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(106068, 'HP:0034638', 'Colonic fibrinopurulent exudate', 'XPO:0100493', 'abnormal liver and biliary system', 0.4411764705882353, 5.05060299610679, 1.4927180591674907, 'HP:0025031', 'Abnormality of the digestive system'),
(106069, 'HP:0034638', 'Colonic fibrinopurulent exudate', 'XPO:0140523', 'abnormally necrotic large intestine', 0.4406779661016949, 10.665155383737162, 2.1679250408314017, 'HP:0002250', 'Abnormal large intestine morphology'),
(106070, 'HP:0034638', 'Colonic fibrinopurulent exudate', 'XPO:0102155', 'abnormal midgut morphology', 0.4090909090909091, 5.725717590856133, 1.5304701939081158, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(106071, 'HP:0034638', 'Colonic fibrinopurulent exudate', 'XPO:0101993', 'abnormal small intestine morphology', 0.42105263157894735, 8.518562886125473, 1.8938752124873177, 'UPHENO:0076783', 'abnormal intestine morphology'),
(106072, 'HP:0034638', 'Colonic fibrinopurulent exudate', 'XPO:0102941', 'abnormal colon morphology', 0.4642857142857143, 10.665155383737162, 2.225236905434237, 'HP:0002250', 'Abnormal large intestine morphology'),
(106073, 'HP:0034638', 'Colonic fibrinopurulent exudate', 'XPO:0115391', 'abnormally undifferentiated alimentary system', 0.4411764705882353, 5.05060299610679, 1.4927180591674907, 'HP:0025031', 'Abnormality of the digestive system'),
(106074, 'HP:0034638', 'Colonic fibrinopurulent exudate', 'XPO:0107288', 'abnormal larval alimentary system', 0.4411764705882353, 5.05060299610679, 1.4927180591674907, 'HP:0025031', 'Abnormality of the digestive system'),
(106075, 'HP:0034638', 'Colonic fibrinopurulent exudate', 'XPO:0100986', 'abnormal gut epithelium', 0.40540540540540543, 5.05060299610679, 1.4309233924911664, 'HP:0025031', 'Abnormality of the digestive system'),
(106076, 'HP:0034638', 'Colonic fibrinopurulent exudate', 'XPO:0102788', 'abnormal typhlosole morphology', 0.43636363636363634, 8.518562886125473, 1.928001835471643, 'UPHENO:0076783', 'abnormal intestine morphology'),
(106077, 'HP:0034638', 'Colonic fibrinopurulent exudate', 'XPO:0102473', 'abnormal large intestine morphology', 0.48148148148148145, 10.665155383737162, 2.266070346302596, 'HP:0002250', 'Abnormal large intestine morphology'),
(106078, 'HP:0034638', 'Colonic fibrinopurulent exudate', 'XPO:0101788', 'abnormal foregut morphology', 0.4090909090909091, 5.725717590856133, 1.5304701939081158, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(106079, 'HP:0034638', 'Colonic fibrinopurulent exudate', 'XPO:0101101', 'abnormal posterior foregut', 0.40540540540540543, 5.05060299610679, 1.4309233924911664, 'HP:0025031', 'Abnormality of the digestive system'),
(106080, 'HP:0034638', 'Colonic fibrinopurulent exudate', 'XPO:0130932', 'increased size of the colon', 0.4126984126984127, 10.665155383737162, 2.0979734741054896, 'HP:0002250', 'Abnormal large intestine morphology'),
(106081, 'HP:0034638', 'Colonic fibrinopurulent exudate', 'XPO:0100462', 'abnormal anterior foregut', 0.40540540540540543, 5.05060299610679, 1.4309233924911664, 'HP:0025031', 'Abnormality of the digestive system'),
(106082, 'HP:0034638', 'Colonic fibrinopurulent exudate', 'XPO:0128144', 'decreased size of the large intestine', 0.4262295081967213, 10.665155383737162, 2.1320891008707643, 'HP:0002250', 'Abnormal large intestine morphology'),
(106083, 'HP:0034638', 'Colonic fibrinopurulent exudate', 'XPO:0103103', 'abnormal rectum morphology', 0.4406779661016949, 10.665155383737162, 2.1679250408314017, 'HP:0002250', 'Abnormal large intestine morphology'),
(106084, 'HP:0034638', 'Colonic fibrinopurulent exudate', 'XPO:0127083', 'abnormally localised ileum', 0.41379310344827586, 8.518562886125473, 1.8774777158648677, 'UPHENO:0076783', 'abnormal intestine morphology'),
(106085, 'HP:0034638', 'Colonic fibrinopurulent exudate', 'XPO:0126693', 'abnormally localised small intestine', 0.41379310344827586, 8.518562886125473, 1.8774777158648677, 'UPHENO:0076783', 'abnormal intestine morphology'),
(106086, 'HP:0034638', 'Colonic fibrinopurulent exudate', 'XPO:0100156', 'abnormal foregut', 0.4166666666666667, 5.05060299610679, 1.45066119926208, 'HP:0025031', 'Abnormality of the digestive system'),
(106087, 'HP:0034638', 'Colonic fibrinopurulent exudate', 'XPO:0102118', 'abnormal oral evagination morphology', 0.4186046511627907, 5.725717590856133, 1.5481640787645816, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(106088, 'HP:0034638', 'Colonic fibrinopurulent exudate', 'XPO:0101471', 'abnormal rectum', 0.52, 10.665155383737162, 2.354969383992778, 'HP:0002250', 'Abnormal large intestine morphology'),
(106089, 'HP:0034638', 'Colonic fibrinopurulent exudate', 'XPO:0101306', 'abnormal ileum', 0.4897959183673469, 8.518562886125473, 2.042634899334637, 'UPHENO:0076783', 'abnormal intestine morphology'),
(106090, 'HP:0034638', 'Colonic fibrinopurulent exudate', 'XPO:0101537', 'abnormal internal coil of the small intestine', 0.4897959183673469, 8.518562886125473, 2.042634899334637, 'UPHENO:0076783', 'abnormal intestine morphology'),
(106091, 'HP:0007267', 'Chronic axonal neuropathy', 'XPO:0101952', 'abnormal lateral line morphology', 0.42, 7.318748312764234, 1.753246785641137, 'HP:0000759', 'Abnormal peripheral nervous system morphology'),
(106092, 'HP:0007267', 'Chronic axonal neuropathy', 'XPO:0102506', 'abnormal occipital lateral line morphology', 0.40384615384615385, 7.318748312764234, 1.7191999177169197, 'HP:0000759', 'Abnormal peripheral nervous system morphology'),
(106093, 'HP:0007267', 'Chronic axonal neuropathy', 'XPO:0101600', 'abnormal Schwann cell', 0.44, 7.318748312764234, 1.7945052960680452, 'HP:0000759', 'Abnormal peripheral nervous system morphology'),
(106094, 'HP:0007267', 'Chronic axonal neuropathy', 'XPO:0102466', 'abnormal ventral lateral line morphology', 0.40384615384615385, 7.318748312764234, 1.7191999177169197, 'HP:0000759', 'Abnormal peripheral nervous system morphology'),
(106095, 'HP:0007267', 'Chronic axonal neuropathy', 'XPO:0102326', 'abnormal lateral line primordium morphology', 0.40384615384615385, 7.318748312764234, 1.7191999177169197, 'HP:0000759', 'Abnormal peripheral nervous system morphology'),
(106096, 'HP:0007267', 'Chronic axonal neuropathy', 'XPO:0100167', 'abnormal nerve', 0.43478260869565216, 7.318748312764234, 1.783834208610917, 'HP:0000759', 'Abnormal peripheral nervous system morphology'),
(106097, 'HP:0007267', 'Chronic axonal neuropathy', 'XPO:0102995', 'abnormal infraorbital lateral line morphology', 0.40384615384615385, 7.318748312764234, 1.7191999177169197, 'HP:0000759', 'Abnormal peripheral nervous system morphology'),
(106098, 'HP:0007267', 'Chronic axonal neuropathy', 'XPO:0102523', 'abnormal dorsal lateral line morphology', 0.40384615384615385, 7.318748312764234, 1.7191999177169197, 'HP:0000759', 'Abnormal peripheral nervous system morphology'),
(106099, 'HP:0007267', 'Chronic axonal neuropathy', 'XPO:0101828', 'abnormal neuron morphology', 0.40425531914893614, 4.7814666189787065, 1.3902997209433732, 'HP:0012639', 'Abnormal nervous system morphology'),
(106100, 'HP:0007267', 'Chronic axonal neuropathy', 'XPO:0102902', 'abnormal caudal lateral line morphology', 0.40384615384615385, 7.318748312764234, 1.7191999177169197, 'HP:0000759', 'Abnormal peripheral nervous system morphology'),
(106101, 'HP:0007267', 'Chronic axonal neuropathy', 'XPO:0101807', 'abnormal migrating neuroblast morphology', 0.40425531914893614, 4.7814666189787065, 1.3902997209433732, 'HP:0012639', 'Abnormal nervous system morphology'),
(106102, 'HP:0007267', 'Chronic axonal neuropathy', 'XPO:0101951', 'abnormal middle lateral line morphology', 0.40384615384615385, 7.318748312764234, 1.7191999177169197, 'HP:0000759', 'Abnormal peripheral nervous system morphology'),
(106103, 'HP:0007267', 'Chronic axonal neuropathy', 'XPO:0101960', 'abnormal supraorbital lateral line morphology', 0.40384615384615385, 7.318748312764234, 1.7191999177169197, 'HP:0000759', 'Abnormal peripheral nervous system morphology'),
(106104, 'HP:0007267', 'Chronic axonal neuropathy', 'XPO:0103198', 'abnormal posterior lateral line morphology', 0.40384615384615385, 7.318748312764234, 1.7191999177169197, 'HP:0000759', 'Abnormal peripheral nervous system morphology'),
(106105, 'HP:0007267', 'Chronic axonal neuropathy', 'XPO:0102670', 'abnormal hyomandibular lateral line morphology', 0.40384615384615385, 7.318748312764234, 1.7191999177169197, 'HP:0000759', 'Abnormal peripheral nervous system morphology'),
(106106, 'HP:0007267', 'Chronic axonal neuropathy', 'XPO:0102366', 'abnormal lateral line system morphology', 0.4375, 7.318748312764234, 1.7894000074981424, 'HP:0000759', 'Abnormal peripheral nervous system morphology'),
(106107, 'HP:0007267', 'Chronic axonal neuropathy', 'XPO:0141286', 'abnormal neuron projection morphology', 0.40425531914893614, 4.7814666189787065, 1.3902997209433732, 'HP:0012639', 'Abnormal nervous system morphology'),
(106108, 'HP:0007267', 'Chronic axonal neuropathy', 'XPO:0101030', 'abnormal spinal nerve', 0.4166666666666667, 7.318748312764234, 1.7462755978515432, 'HP:0000759', 'Abnormal peripheral nervous system morphology'),
(106109, 'HP:0007267', 'Chronic axonal neuropathy', 'XPO:0139791', 'abnormally necrotic peripheral nervous system', 0.40384615384615385, 7.318748312764234, 1.7191999177169197, 'HP:0000759', 'Abnormal peripheral nervous system morphology'),
(106110, 'HP:0007267', 'Chronic axonal neuropathy', 'XPO:0102334', 'abnormal glial cell morphology', 0.40425531914893614, 4.7814666189787065, 1.3902997209433732, 'HP:0012639', 'Abnormal nervous system morphology'),
(106111, 'HP:0007267', 'Chronic axonal neuropathy', 'XPO:0102747', 'abnormal trunk lateral line morphology', 0.40384615384615385, 7.318748312764234, 1.7191999177169197, 'HP:0000759', 'Abnormal peripheral nervous system morphology'),
(106112, 'HP:0007267', 'Chronic axonal neuropathy', 'XPO:0101746', 'abnormal peripheral nervous system morphology', 0.45652173913043476, 7.318748312764234, 1.8278861310270569, 'HP:0000759', 'Abnormal peripheral nervous system morphology'),
(106113, 'HP:0007267', 'Chronic axonal neuropathy', 'XPO:0101204', 'abnormal peripheral nerve', 0.43478260869565216, 7.318748312764234, 1.783834208610917, 'HP:0000759', 'Abnormal peripheral nervous system morphology'),
(106114, 'HP:0007267', 'Chronic axonal neuropathy', 'XPO:0101990', 'abnormal ganglion morphology', 0.40384615384615385, 7.318748312764234, 1.7191999177169197, 'HP:0000759', 'Abnormal peripheral nervous system morphology'),
(106115, 'HP:0007267', 'Chronic axonal neuropathy', 'XPO:0133431', 'abnormal cilium morphology in the lateral line', 0.42592592592592593, 7.318748312764234, 1.765572046599321, 'HP:0000759', 'Abnormal peripheral nervous system morphology'),
(106116, 'HP:0031314', 'Carotid artery calcification', 'XPO:0102619', 'abnormal larval aorta morphology', 0.41935483870967744, 9.01729298920255, 1.9445939028714816, 'UPHENO:0015290', 'abnormal artery morphology in the independent continuant'),
(106117, 'HP:0031314', 'Carotid artery calcification', 'XPO:0101708', 'abnormal artery morphology', 0.43333333333333335, 9.01729298920255, 1.976738128497156, 'UPHENO:0015290', 'abnormal artery morphology in the independent continuant'),
(106118, 'HP:0031314', 'Carotid artery calcification', 'XPO:0101052', 'abnormal ophthalmic artery', 0.40789473684210525, 11.341685124041394, 2.1508634705663874, 'UPHENO:0087623', 'abnormal carotid artery segment morphology'),
(106119, 'HP:0031314', 'Carotid artery calcification', 'XPO:0102329', 'abnormal caudal artery morphology', 0.4166666666666667, 9.08792853179561, 1.945928284456591, 'UPHENO:0087334', 'abnormal systemic artery morphology'),
(106120, 'HP:0031314', 'Carotid artery calcification', 'XPO:0101780', 'abnormal arteria mesenterica posterior morphology', 0.410958904109589, 9.08792853179561, 1.932554048417014, 'UPHENO:0087334', 'abnormal systemic artery morphology'),
(106121, 'HP:0031314', 'Carotid artery calcification', 'XPO:0101154', 'abnormal external carotid artery', 0.42028985507246375, 9.08792853179561, 1.9543705292337186, 'UPHENO:0087334', 'abnormal systemic artery morphology'),
(106122, 'HP:0031314', 'Carotid artery calcification', 'XPO:0103091', 'abnormal arteria iliaca communis morphology', 0.4225352112676056, 9.08792853179561, 1.9595840890778735, 'UPHENO:0087334', 'abnormal systemic artery morphology'),
(106123, 'HP:0031314', 'Carotid artery calcification', 'XPO:0102875', 'abnormal vertebral artery morphology', 0.41935483870967744, 9.01729298920255, 1.9445939028714816, 'UPHENO:0015290', 'abnormal artery morphology in the independent continuant'),
(106124, 'HP:0031314', 'Carotid artery calcification', 'XPO:0102412', 'abnormal vascular plexus morphology', 0.4166666666666667, 9.077623523403872, 1.9448247054044776, 'UPHENO:0015321', 'abnormal vasculature morphology in the independent continuant'),
(106125, 'HP:0031314', 'Carotid artery calcification', 'XPO:0101712', 'abnormal aorta morphology', 0.45454545454545453, 9.08792853179561, 2.0324558064965745, 'UPHENO:0087334', 'abnormal systemic artery morphology'),
(106126, 'HP:0031314', 'Carotid artery calcification', 'XPO:0101774', 'abnormal paired dorsal aorta morphology', 0.4411764705882353, 9.08792853179561, 2.0023436854385688, 'UPHENO:0087334', 'abnormal systemic artery morphology'),
(106127, 'HP:0031314', 'Carotid artery calcification', 'XPO:0103063', 'abnormal ischiadic artery morphology', 0.41935483870967744, 9.01729298920255, 1.9445939028714816, 'UPHENO:0015290', 'abnormal artery morphology in the independent continuant'),
(106128, 'HP:0031314', 'Carotid artery calcification', 'XPO:0102421', 'abnormal occipitovertebral artery morphology', 0.41935483870967744, 9.01729298920255, 1.9445939028714816, 'UPHENO:0015290', 'abnormal artery morphology in the independent continuant'),
(106129, 'HP:0031314', 'Carotid artery calcification', 'XPO:0101686', 'abnormal blood vessel morphology', 0.41379310344827586, 6.974839882869777, 1.6988645152534954, 'UPHENO:0087186', 'abnormal blood vessel morphology'),
(106130, 'HP:0031314', 'Carotid artery calcification', 'XPO:0101711', 'abnormal dorsal aorta morphology', 0.410958904109589, 9.08792853179561, 1.932554048417014, 'UPHENO:0087334', 'abnormal systemic artery morphology'),
(106131, 'HP:0031314', 'Carotid artery calcification', 'XPO:0101840', 'abnormal ventral aorta morphology', 0.410958904109589, 9.08792853179561, 1.932554048417014, 'UPHENO:0087334', 'abnormal systemic artery morphology'),
(106132, 'HP:0031314', 'Carotid artery calcification', 'XPO:0139803', 'abnormally necrotic aorta', 0.410958904109589, 9.08792853179561, 1.932554048417014, 'UPHENO:0087334', 'abnormal systemic artery morphology'),
(106133, 'HP:0002299', 'Brittle hair', 'XPO:0102945', 'abnormal Eberth-Kastschenko layer morphology', 0.42, 7.420886955069779, 1.7654383368244009, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(106134, 'HP:0002299', 'Brittle hair', 'XPO:0102176', 'abnormal neuromast support cell morphology', 0.42, 7.420886955069779, 1.7654383368244009, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(106135, 'HP:0002299', 'Brittle hair', 'XPO:0102561', 'abnormal dermis morphology', 0.4375, 7.420886955069779, 1.8018429573198183, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(106136, 'HP:0002299', 'Brittle hair', 'XPO:0102727', 'abnormal skin seromucous gland morphology', 0.42857142857142855, 7.420886955069779, 1.7833620281931915, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(106137, 'HP:0002299', 'Brittle hair', 'XPO:0102626', 'abnormal granular gland morphology', 0.42857142857142855, 7.420886955069779, 1.7833620281931915, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(106138, 'HP:0002299', 'Brittle hair', 'XPO:0102840', 'abnormal stratum spongiosum morphology', 0.42, 7.420886955069779, 1.7654383368244009, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(106139, 'HP:0002299', 'Brittle hair', 'XPO:0103147', 'abnormal neuromast mantle cell morphology', 0.42, 7.420886955069779, 1.7654383368244009, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(106140, 'HP:0002299', 'Brittle hair', 'XPO:0102139', 'abnormal skin morphology', 0.44680851063829785, 7.420886955069779, 1.8209106095604752, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(106141, 'HP:0002299', 'Brittle hair', 'XPO:0102886', 'abnormal stratum compactum morphology', 0.42, 7.420886955069779, 1.7654383368244009, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(106142, 'HP:0002299', 'Brittle hair', 'XPO:0102615', 'abnormal skin gland morphology', 0.44680851063829785, 7.420886955069779, 1.8209106095604752, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(106143, 'HP:0002299', 'Brittle hair', 'XPO:0102910', 'abnormal pigment cell morphology', 0.42, 7.420886955069779, 1.7654383368244009, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(106144, 'HP:0002299', 'Brittle hair', 'XPO:0103019', 'abnormal melanophore morphology', 0.40384615384615385, 7.420886955069779, 1.7311547172139254, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(106145, 'HP:0002299', 'Brittle hair', 'XPO:0102954', 'abnormal iridophore morphology', 0.40384615384615385, 7.420886955069779, 1.7311547172139254, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(106146, 'HP:0002299', 'Brittle hair', 'XPO:0103223', 'abnormal xanthophore morphology', 0.40384615384615385, 7.420886955069779, 1.7311547172139254, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(106147, 'HP:0003750', 'Increased muscle fatiguability', 'XPO:0100746', 'abnormal smooth muscle', 0.4117647058823529, 5.968280811662945, 1.5676502776568768, 'UPHENO:0002816', 'abnormal musculature'),
(106148, 'HP:0003750', 'Increased muscle fatiguability', 'XPO:0100100', 'abnormal muscle', 0.42424242424242425, 5.968280811662945, 1.591225288920281, 'UPHENO:0002816', 'abnormal musculature'),
(106149, 'HP:0003750', 'Increased muscle fatiguability', 'XPO:0100275', 'abnormal skeletal muscle', 0.4117647058823529, 5.968280811662945, 1.5676502776568768, 'UPHENO:0002816', 'abnormal musculature'),
(106150, 'HP:0032024', 'Ileal ulcer', 'XPO:0107375', 'abnormal larval alimentary system morphology', 0.4375, 5.725717590856133, 1.582719635943005, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(106151, 'HP:0032024', 'Ileal ulcer', 'XPO:0130328', 'increased size of the internal coil of the small intestine', 0.4626865671641791, 10.973645104299719, 2.2532993992335855, 'UPHENO:0086621', 'abnormal small intestine morphology'),
(106152, 'HP:0032024', 'Ileal ulcer', 'XPO:0107381', 'abnormal intestinal stem cell morphology', 0.4696969696969697, 10.973645104299719, 2.2703056736967304, 'UPHENO:0086621', 'abnormal small intestine morphology'),
(106153, 'HP:0032024', 'Ileal ulcer', 'XPO:0102953', 'abnormal duodenum morphology', 0.5, 10.973645104299719, 2.3423967537865695, 'UPHENO:0086621', 'abnormal small intestine morphology'),
(106154, 'HP:0032024', 'Ileal ulcer', 'XPO:0140675', 'abnormally necrotic duodenum', 0.4626865671641791, 10.973645104299719, 2.2532993992335855, 'UPHENO:0086621', 'abnormal small intestine morphology'),
(106155, 'HP:0032024', 'Ileal ulcer', 'XPO:0102155', 'abnormal midgut morphology', 0.42, 5.725717590856133, 1.5507422055775666, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(106156, 'HP:0032024', 'Ileal ulcer', 'XPO:0127665', 'abnormally localised duodenum', 0.4153846153846154, 10.103525386846629, 2.0486212453364785, 'HP:0002244', 'Abnormal small intestine morphology'),
(106157, 'HP:0032024', 'Ileal ulcer', 'XPO:0139794', 'abnormally necrotic small intestine', 0.484375, 10.973645104299719, 2.3055063104218942, 'UPHENO:0086621', 'abnormal small intestine morphology'),
(106158, 'HP:0032024', 'Ileal ulcer', 'XPO:0102156', 'abnormal intestine morphology', 0.4444444444444444, 9.054702908261955, 2.0060688930522748, 'UPHENO:0084771', 'abnormal anatomical entity morphology in the alimentary part of gastrointestinal system'),
(106159, 'HP:0032024', 'Ileal ulcer', 'XPO:0101306', 'abnormal ileum', 0.4642857142857143, 10.103525386846629, 2.165853757998433, 'HP:0002244', 'Abnormal small intestine morphology'),
(106160, 'HP:0032024', 'Ileal ulcer', 'XPO:0102429', 'abnormal esophagus morphology', 0.4098360655737705, 8.037124161124119, 1.8149113875677236, 'UPHENO:0076735', 'abnormal alimentary part of gastrointestinal system morphology'),
(106161, 'HP:0032024', 'Ileal ulcer', 'XPO:0102473', 'abnormal large intestine morphology', 0.45901639344262296, 9.054702908261955, 2.0386900383934856, 'UPHENO:0084771', 'abnormal anatomical entity morphology in the alimentary part of gastrointestinal system'),
(106162, 'HP:0032024', 'Ileal ulcer', 'XPO:0103013', 'abnormal ventral foregut morphology', 0.4117647058823529, 5.725717590856133, 1.5354635846428564, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(106163, 'HP:0032024', 'Ileal ulcer', 'XPO:0101784', 'abnormal alimentary system morphology', 0.45652173913043476, 5.725717590856133, 1.6167605117479105, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(106164, 'HP:0032024', 'Ileal ulcer', 'XPO:0115766', 'abnormally inverted external coil of the small intestine', 0.5081967213114754, 10.973645104299719, 2.3615186772161767, 'UPHENO:0086621', 'abnormal small intestine morphology'),
(106165, 'HP:0032024', 'Ileal ulcer', 'XPO:0139906', 'abnormally necrotic alimentary system', 0.4117647058823529, 5.725717590856133, 1.5354635846428564, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(106166, 'HP:0032024', 'Ileal ulcer', 'XPO:0126693', 'abnormally localised small intestine', 0.421875, 10.103525386846629, 2.064564063567881, 'HP:0002244', 'Abnormal small intestine morphology'),
(106167, 'HP:0032024', 'Ileal ulcer', 'XPO:0130900', 'increased size of the external coil of the small intestine', 0.4626865671641791, 10.973645104299719, 2.2532993992335855, 'UPHENO:0086621', 'abnormal small intestine morphology'),
(106168, 'HP:0032024', 'Ileal ulcer', 'XPO:0101288', 'abnormal external coil of the small intestine', 0.4642857142857143, 10.103525386846629, 2.165853757998433, 'HP:0002244', 'Abnormal small intestine morphology'),
(106169, 'HP:0032024', 'Ileal ulcer', 'XPO:0140409', 'abnormally necrotic typhlosole', 0.4307692307692308, 9.054702908261955, 1.9749651659297485, 'UPHENO:0084771', 'abnormal anatomical entity morphology in the alimentary part of gastrointestinal system'),
(106170, 'HP:0032024', 'Ileal ulcer', 'XPO:0128283', 'decreased size of the small intestine', 0.4696969696969697, 10.973645104299719, 2.2703056736967304, 'UPHENO:0086621', 'abnormal small intestine morphology'),
(106171, 'HP:0032024', 'Ileal ulcer', 'XPO:0140074', 'abnormally necrotic intestinal stem cell', 0.43661971830985913, 10.973645104299719, 2.1889060816471106, 'UPHENO:0086621', 'abnormal small intestine morphology'),
(106172, 'HP:0032024', 'Ileal ulcer', 'XPO:0140523', 'abnormally necrotic large intestine', 0.42424242424242425, 9.054702908261955, 1.9599462014545146, 'UPHENO:0084771', 'abnormal anatomical entity morphology in the alimentary part of gastrointestinal system'),
(106173, 'HP:0032024', 'Ileal ulcer', 'XPO:0102733', 'abnormal posterior foregut morphology', 0.4117647058823529, 5.725717590856133, 1.5354635846428564, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(106174, 'HP:0032024', 'Ileal ulcer', 'XPO:0133341', 'abnormally coiled small intestine', 0.4696969696969697, 10.973645104299719, 2.2703056736967304, 'UPHENO:0086621', 'abnormal small intestine morphology'),
(106175, 'HP:0032024', 'Ileal ulcer', 'XPO:0100361', 'abnormal small intestine', 0.4727272727272727, 10.103525386846629, 2.1854546440168394, 'HP:0002244', 'Abnormal small intestine morphology'),
(106176, 'HP:0032024', 'Ileal ulcer', 'XPO:0101537', 'abnormal internal coil of the small intestine', 0.4642857142857143, 10.103525386846629, 2.165853757998433, 'HP:0002244', 'Abnormal small intestine morphology'),
(106177, 'HP:0032024', 'Ileal ulcer', 'XPO:0101321', 'abnormal duodenum', 0.4642857142857143, 10.103525386846629, 2.165853757998433, 'HP:0002244', 'Abnormal small intestine morphology'),
(106178, 'HP:0032024', 'Ileal ulcer', 'XPO:0140907', 'abnormally necrotic internal coil of the small intestine', 0.47692307692307695, 10.973645104299719, 2.287702906455399, 'UPHENO:0086621', 'abnormal small intestine morphology'),
(106179, 'HP:0032024', 'Ileal ulcer', 'XPO:0102618', 'abnormal gut epithelium morphology', 0.4117647058823529, 5.725717590856133, 1.5354635846428564, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(106180, 'HP:0032024', 'Ileal ulcer', 'XPO:0103334', 'decreased size of the duodenum', 0.4492753623188406, 10.973645104299719, 2.2204027517981118, 'UPHENO:0086621', 'abnormal small intestine morphology'),
(106181, 'HP:0032024', 'Ileal ulcer', 'XPO:0101993', 'abnormal small intestine morphology', 0.5254237288135594, 10.973645104299719, 2.4012108465059496, 'UPHENO:0086621', 'abnormal small intestine morphology'),
(106182, 'HP:0032024', 'Ileal ulcer', 'XPO:0129426', 'decreased size of the external coil of the small intestine', 0.4626865671641791, 10.973645104299719, 2.2532993992335855, 'UPHENO:0086621', 'abnormal small intestine morphology'),
(106183, 'HP:0032024', 'Ileal ulcer', 'XPO:0129821', 'increased size of the pharyngeal cavity', 0.4117647058823529, 5.725717590856133, 1.5354635846428564, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(106184, 'HP:0032024', 'Ileal ulcer', 'XPO:0129763', 'increased size of the small intestine', 0.4696969696969697, 10.973645104299719, 2.2703056736967304, 'UPHENO:0086621', 'abnormal small intestine morphology'),
(106185, 'HP:0032024', 'Ileal ulcer', 'XPO:0102938', 'abnormal ileum morphology', 0.5666666666666667, 13.964122330181212, 2.813005981822533, 'HP:0001549', 'Abnormal ileum morphology'),
(106186, 'HP:0032024', 'Ileal ulcer', 'XPO:0127587', 'abnormally localised external coil of the small intestine', 0.421875, 10.103525386846629, 2.064564063567881, 'HP:0002244', 'Abnormal small intestine morphology'),
(106187, 'HP:0032024', 'Ileal ulcer', 'XPO:0133351', 'abnormally decreased coiling of external coil of the small intestine', 0.4492753623188406, 10.973645104299719, 2.2204027517981118, 'UPHENO:0086621', 'abnormal small intestine morphology'),
(106188, 'HP:0032024', 'Ileal ulcer', 'XPO:0133350', 'abnormally decreased coiling of small intestine', 0.4492753623188406, 10.973645104299719, 2.2204027517981118, 'UPHENO:0086621', 'abnormal small intestine morphology'),
(106189, 'HP:0032024', 'Ileal ulcer', 'XPO:0139726', 'abnormally necrotic colon', 0.4057971014492754, 9.054702908261955, 1.9168651999180917, 'UPHENO:0084771', 'abnormal anatomical entity morphology in the alimentary part of gastrointestinal system'),
(106190, 'HP:0032024', 'Ileal ulcer', 'XPO:0141833', 'edematous alimentary system', 0.4375, 5.725717590856133, 1.582719635943005, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(106191, 'HP:0032024', 'Ileal ulcer', 'XPO:0129624', 'increased size of the large intestine', 0.4117647058823529, 9.054702908261955, 1.9309083561558715, 'UPHENO:0084771', 'abnormal anatomical entity morphology in the alimentary part of gastrointestinal system'),
(106192, 'HP:0032024', 'Ileal ulcer', 'XPO:0129234', 'decreased size of the ileum', 0.5074626865671642, 13.964122330181212, 2.662005077610914, 'HP:0001549', 'Abnormal ileum morphology'),
(106193, 'HP:0032024', 'Ileal ulcer', 'XPO:0128850', 'decreased size of the internal coil of the small intestine', 0.4626865671641791, 10.973645104299719, 2.2532993992335855, 'UPHENO:0086621', 'abnormal small intestine morphology'),
(106194, 'HP:0032024', 'Ileal ulcer', 'XPO:0140953', 'abnormally necrotic external coil of the small intestine', 0.47692307692307695, 10.973645104299719, 2.287702906455399, 'UPHENO:0086621', 'abnormal small intestine morphology'),
(106195, 'HP:0032024', 'Ileal ulcer', 'XPO:0130710', 'increased size of the ileum', 0.5, 13.964122330181212, 2.642359015177651, 'HP:0001549', 'Abnormal ileum morphology'),
(106196, 'HP:0032024', 'Ileal ulcer', 'XPO:0133432', 'abnormal cilium morphology in the alimentary system', 0.40384615384615385, 5.725717590856133, 1.520627839767678, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(106197, 'HP:0032024', 'Ileal ulcer', 'XPO:0115392', 'abnormally incomplete structure of alimentary system', 0.44680851063829785, 5.725717590856133, 1.5994684583029237, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(106198, 'HP:0032024', 'Ileal ulcer', 'XPO:0128341', 'decreased size of the pharyngeal cavity', 0.4117647058823529, 5.725717590856133, 1.5354635846428564, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(106199, 'HP:0032024', 'Ileal ulcer', 'XPO:0102118', 'abnormal oral evagination morphology', 0.42857142857142855, 5.725717590856133, 1.5664861849086864, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(106200, 'HP:0032024', 'Ileal ulcer', 'XPO:0126463', 'abnormally localised internal coil of the small intestine', 0.421875, 10.103525386846629, 2.064564063567881, 'HP:0002244', 'Abnormal small intestine morphology'),
(106201, 'HP:0032024', 'Ileal ulcer', 'XPO:0127083', 'abnormally localised ileum', 0.421875, 10.103525386846629, 2.064564063567881, 'HP:0002244', 'Abnormal small intestine morphology'),
(106202, 'HP:0032024', 'Ileal ulcer', 'XPO:0128144', 'decreased size of the large intestine', 0.4117647058823529, 9.054702908261955, 1.9309083561558715, 'UPHENO:0084771', 'abnormal anatomical entity morphology in the alimentary part of gastrointestinal system'),
(106203, 'HP:0032024', 'Ileal ulcer', 'XPO:0102653', 'abnormal dorsal foregut morphology', 0.4117647058823529, 5.725717590856133, 1.5354635846428564, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(106204, 'HP:0032024', 'Ileal ulcer', 'XPO:0102788', 'abnormal typhlosole morphology', 0.4666666666666667, 9.054702908261955, 2.0556089180229735, 'UPHENO:0084771', 'abnormal anatomical entity morphology in the alimentary part of gastrointestinal system'),
(106205, 'HP:0032024', 'Ileal ulcer', 'XPO:0103169', 'abnormal internal coil of the small intestine morphology', 0.5166666666666667, 10.973645104299719, 2.3811166786240276, 'UPHENO:0086621', 'abnormal small intestine morphology'),
(106206, 'HP:0032024', 'Ileal ulcer', 'XPO:0141642', 'neoplastic intestine', 0.42424242424242425, 9.054702908261955, 1.9599462014545146, 'UPHENO:0084771', 'abnormal anatomical entity morphology in the alimentary part of gastrointestinal system'),
(106207, 'HP:0032024', 'Ileal ulcer', 'XPO:0107294', 'abnormal intestinal stem cell', 0.43333333333333335, 10.103525386846629, 2.0924135189537, 'HP:0002244', 'Abnormal small intestine morphology'),
(106208, 'HP:0032024', 'Ileal ulcer', 'XPO:0102125', 'abnormal liver and biliary system morphology', 0.4375, 5.725717590856133, 1.582719635943005, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(106209, 'HP:0032024', 'Ileal ulcer', 'XPO:0102941', 'abnormal colon morphology', 0.4444444444444444, 9.054702908261955, 2.0060688930522748, 'UPHENO:0084771', 'abnormal anatomical entity morphology in the alimentary part of gastrointestinal system'),
(106210, 'HP:0032024', 'Ileal ulcer', 'XPO:0102367', 'abnormal hindgut morphology', 0.42, 5.725717590856133, 1.5507422055775666, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(106211, 'HP:0032024', 'Ileal ulcer', 'XPO:0129412', 'decreased size of the typhlosole', 0.417910447761194, 9.054702908261955, 1.9452647497799211, 'UPHENO:0084771', 'abnormal anatomical entity morphology in the alimentary part of gastrointestinal system'),
(106212, 'HP:0032024', 'Ileal ulcer', 'XPO:0103723', 'increased size of the duodenum', 0.44285714285714284, 10.973645104299719, 2.2044856809737836, 'UPHENO:0086621', 'abnormal small intestine morphology'),
(106213, 'HP:0032024', 'Ileal ulcer', 'XPO:0101788', 'abnormal foregut morphology', 0.42, 5.725717590856133, 1.5507422055775666, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(106214, 'HP:0032024', 'Ileal ulcer', 'XPO:0102920', 'abnormal external coil of the small intestine morphology', 0.5166666666666667, 10.973645104299719, 2.3811166786240276, 'UPHENO:0086621', 'abnormal small intestine morphology'),
(106215, 'HP:0032024', 'Ileal ulcer', 'XPO:0102522', 'abnormal pharyngeal cavity morphology', 0.45652173913043476, 5.725717590856133, 1.6167605117479105, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(106216, 'HP:0032024', 'Ileal ulcer', 'XPO:0130886', 'increased size of the typhlosole', 0.417910447761194, 9.054702908261955, 1.9452647497799211, 'UPHENO:0084771', 'abnormal anatomical entity morphology in the alimentary part of gastrointestinal system'),
(106217, 'HP:0032024', 'Ileal ulcer', 'XPO:0142061', 'abnormal digestive tract morphology', 0.4375, 5.725717590856133, 1.582719635943005, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(106218, 'HP:0032024', 'Ileal ulcer', 'XPO:0140419', 'abnormally necrotic ileum', 0.5230769230769231, 13.964122330181212, 2.7026487270714523, 'HP:0001549', 'Abnormal ileum morphology'),
(106219, 'HP:0032024', 'Ileal ulcer', 'XPO:0141834', 'edematous foregut', 0.40384615384615385, 5.725717590856133, 1.520627839767678, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(106220, 'HP:0032024', 'Ileal ulcer', 'XPO:0133352', 'abnormally decreased coiling of internal coil of the small intestine', 0.4492753623188406, 10.973645104299719, 2.2204027517981118, 'UPHENO:0086621', 'abnormal small intestine morphology'),
(106221, 'HP:0032024', 'Ileal ulcer', 'XPO:0102094', 'abnormal anterior foregut morphology', 0.4117647058823529, 5.725717590856133, 1.5354635846428564, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(106222, 'HP:0032024', 'Ileal ulcer', 'XPO:0103103', 'abnormal rectum morphology', 0.42424242424242425, 9.054702908261955, 1.9599462014545146, 'UPHENO:0084771', 'abnormal anatomical entity morphology in the alimentary part of gastrointestinal system'),
(106223, 'HP:0032024', 'Ileal ulcer', 'XPO:0103009', 'abnormal manicotto glandulare morphology', 0.42857142857142855, 5.725717590856133, 1.5664861849086864, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(106224, 'HP:0032024', 'Ileal ulcer', 'XPO:0125073', 'absent small intestine', 0.4090909090909091, 10.103525386846629, 2.033042150455363, 'HP:0002244', 'Abnormal small intestine morphology'),
(106225, 'HP:0025326', 'Retinal arterial occlusion', 'XPO:0140271', 'abnormally necrotic peripheral retina', 0.43137254901960786, 8.767034997756374, 1.9447000371075944, 'UPHENO:0015314', 'abnormal anatomical entity morphology in the retina'),
(106226, 'HP:0025326', 'Retinal arterial occlusion', 'XPO:0102450', 'abnormal retinal stem cell morphology', 0.41509433962264153, 8.767034997756374, 1.9076547388985956, 'UPHENO:0015314', 'abnormal anatomical entity morphology in the retina'),
(106227, 'HP:0025326', 'Retinal arterial occlusion', 'XPO:0128330', 'decreased size of the retinal progenitor cell region', 0.43137254901960786, 8.767034997756374, 1.9447000371075944, 'UPHENO:0015314', 'abnormal anatomical entity morphology in the retina'),
(106228, 'HP:0025326', 'Retinal arterial occlusion', 'XPO:0102117', 'abnormal retina morphology', 0.4574468085106383, 8.040873045973026, 1.9178820903589395, 'HP:0000479', 'Abnormal retinal morphology'),
(106229, 'HP:0025326', 'Retinal arterial occlusion', 'XPO:0102196', 'abnormal central retina morphology', 0.4731182795698925, 8.767034997756374, 2.036625767063633, 'UPHENO:0015314', 'abnormal anatomical entity morphology in the retina'),
(106230, 'HP:0025326', 'Retinal arterial occlusion', 'XPO:0102581', 'abnormal outer limiting membrane morphology', 0.411214953271028, 8.767034997756374, 1.898719538775502, 'UPHENO:0015314', 'abnormal anatomical entity morphology in the retina'),
(106231, 'HP:0025326', 'Retinal arterial occlusion', 'XPO:0130257', 'increased size of the retinal blood vessel', 0.6138613861386139, 12.189682030596343, 2.735466159156575, 'UPHENO:0087970', 'abnormal retina blood vessel morphology'),
(106232, 'HP:0025326', 'Retinal arterial occlusion', 'XPO:0140489', 'abnormally necrotic ciliary marginal zone', 0.4036697247706422, 8.767034997756374, 1.8812194461569078, 'UPHENO:0015314', 'abnormal anatomical entity morphology in the retina'),
(106233, 'HP:0025326', 'Retinal arterial occlusion', 'XPO:0128475', 'decreased size of the retinal stem cell region', 0.43137254901960786, 8.767034997756374, 1.9447000371075944, 'UPHENO:0015314', 'abnormal anatomical entity morphology in the retina'),
(106234, 'HP:0025326', 'Retinal arterial occlusion', 'XPO:0102947', 'abnormal hyaloid vascular plexus morphology', 0.4639175257731959, 10.24626555896271, 2.1802344292596363, 'UPHENO:0087915', 'abnormal vasculature of eye morphology'),
(106235, 'HP:0025326', 'Retinal arterial occlusion', 'XPO:0140732', 'abnormally necrotic hyaloid artery', 0.4434782608695652, 10.24626555896271, 2.131665084035601, 'UPHENO:0087915', 'abnormal vasculature of eye morphology'),
(106236, 'HP:0025326', 'Retinal arterial occlusion', 'XPO:0128643', 'decreased size of the retinal layer', 0.4489795918367347, 8.767034997756374, 1.9839908757126443, 'UPHENO:0015314', 'abnormal anatomical entity morphology in the retina'),
(106237, 'HP:0025326', 'Retinal arterial occlusion', 'XPO:0100371', 'abnormal hyaloid blood vessel', 0.43529411764705883, 9.463856994035337, 2.029670239166096, 'UPHENO:0005090', 'abnormal vasculature of eye'),
(106238, 'HP:0025326', 'Retinal arterial occlusion', 'XPO:0102946', 'abnormal retinal inner nuclear layer morphology', 0.411214953271028, 8.767034997756374, 1.898719538775502, 'UPHENO:0015314', 'abnormal anatomical entity morphology in the retina'),
(106239, 'HP:0025326', 'Retinal arterial occlusion', 'XPO:0129045', 'decreased size of the hyaloid vein', 0.42990654205607476, 10.24626555896271, 2.0987940812385366, 'UPHENO:0087915', 'abnormal vasculature of eye morphology'),
(106240, 'HP:0025326', 'Retinal arterial occlusion', 'XPO:0102963', 'abnormal retinal outer nuclear layer morphology', 0.411214953271028, 8.767034997756374, 1.898719538775502, 'UPHENO:0015314', 'abnormal anatomical entity morphology in the retina'),
(106241, 'HP:0025326', 'Retinal arterial occlusion', 'XPO:0129355', 'decreased size of the hyaloid vascular plexus', 0.4166666666666667, 10.24626555896271, 2.0662229589844516, 'UPHENO:0087915', 'abnormal vasculature of eye morphology'),
(106242, 'HP:0025326', 'Retinal arterial occlusion', 'XPO:0130013', 'increased size of the optic choroid vascular plexus', 0.4636363636363636, 10.24626555896271, 2.179573652026924, 'UPHENO:0087915', 'abnormal vasculature of eye morphology'),
(106243, 'HP:0025326', 'Retinal arterial occlusion', 'XPO:0100329', 'abnormal retinal blood vessel', 0.6, 11.457162341461329, 2.6218881373690976, 'UPHENO:0005091', 'abnormal vasculature of retina'),
(106244, 'HP:0025326', 'Retinal arterial occlusion', 'XPO:0102991', 'abnormal hyaloid artery morphology', 0.4766355140186916, 10.24626555896271, 2.2099172046636064, 'UPHENO:0087915', 'abnormal vasculature of eye morphology'),
(106245, 'HP:0025326', 'Retinal arterial occlusion', 'XPO:0128564', 'decreased size of the hyaloid blood vessel', 0.45918367346938777, 10.24626555896271, 2.1690822618580805, 'UPHENO:0087915', 'abnormal vasculature of eye morphology'),
(106246, 'HP:0025326', 'Retinal arterial occlusion', 'XPO:0129955', 'increased size of the retinal stem cell region', 0.43137254901960786, 8.767034997756374, 1.9447000371075944, 'UPHENO:0015314', 'abnormal anatomical entity morphology in the retina'),
(106247, 'HP:0025326', 'Retinal arterial occlusion', 'XPO:0130265', 'increased size of the peripheral retina', 0.4230769230769231, 8.767034997756374, 1.925910224117019, 'UPHENO:0015314', 'abnormal anatomical entity morphology in the retina'),
(106248, 'HP:0025326', 'Retinal arterial occlusion', 'XPO:0102505', 'abnormal retinal stem cell region morphology', 0.4536082474226804, 8.767034997756374, 1.9941914101774614, 'UPHENO:0015314', 'abnormal anatomical entity morphology in the retina'),
(106249, 'HP:0025326', 'Retinal arterial occlusion', 'XPO:0102939', 'abnormal retinal ganglion cell layer morphology', 0.411214953271028, 8.767034997756374, 1.898719538775502, 'UPHENO:0015314', 'abnormal anatomical entity morphology in the retina'),
(106250, 'HP:0025326', 'Retinal arterial occlusion', 'XPO:0129309', 'decreased size of the hyaloid artery', 0.4358974358974359, 10.24626555896271, 2.113367191161075, 'UPHENO:0087915', 'abnormal vasculature of eye morphology'),
(106251, 'HP:0025326', 'Retinal arterial occlusion', 'XPO:0140192', 'abnormally necrotic retina', 0.43434343434343436, 8.040873045973026, 1.8688232698432123, 'HP:0000479', 'Abnormal retinal morphology'),
(106252, 'HP:0025326', 'Retinal arterial occlusion', 'XPO:0128300', 'decreased size of the retina', 0.42574257425742573, 8.040873045973026, 1.850227550835222, 'HP:0000479', 'Abnormal retinal morphology'),
(106253, 'HP:0025326', 'Retinal arterial occlusion', 'XPO:0128533', 'decreased size of the optic choroid vascular plexus', 0.4636363636363636, 10.24626555896271, 2.179573652026924, 'UPHENO:0087915', 'abnormal vasculature of eye morphology'),
(106254, 'HP:0025326', 'Retinal arterial occlusion', 'XPO:0140391', 'abnormally necrotic central retina', 0.4583333333333333, 8.767034997756374, 2.004550915784299, 'UPHENO:0015314', 'abnormal anatomical entity morphology in the retina'),
(106255, 'HP:0025326', 'Retinal arterial occlusion', 'XPO:0130122', 'increased size of the retinal layer', 0.4489795918367347, 8.767034997756374, 1.9839908757126443, 'UPHENO:0015314', 'abnormal anatomical entity morphology in the retina'),
(106256, 'HP:0025326', 'Retinal arterial occlusion', 'XPO:0101315', 'abnormal hyaloid vascular plexus', 0.42528735632183906, 9.463856994035337, 2.0062050547242762, 'HP:0008047', 'Abnormality of the vasculature of the eye'),
(106257, 'HP:0025326', 'Retinal arterial occlusion', 'XPO:0102411', 'abnormal optic choroid vascular plexus morphology', 0.51, 10.24626555896271, 2.2859561314843693, 'UPHENO:0087915', 'abnormal vasculature of eye morphology'),
(106258, 'HP:0025326', 'Retinal arterial occlusion', 'XPO:0130785', 'increased size of the hyaloid artery', 0.4358974358974359, 10.24626555896271, 2.113367191161075, 'UPHENO:0087915', 'abnormal vasculature of eye morphology'),
(106259, 'HP:0025326', 'Retinal arterial occlusion', 'XPO:0140531', 'abnormally necrotic retinal progenitor cell region', 0.44, 8.767034997756374, 1.9640507628401067, 'UPHENO:0015314', 'abnormal anatomical entity morphology in the retina'),
(106260, 'HP:0025326', 'Retinal arterial occlusion', 'XPO:0102756', 'abnormal Muller cell morphology', 0.43564356435643564, 8.767034997756374, 1.9543035524862054, 'UPHENO:0015314', 'abnormal anatomical entity morphology in the retina'),
(106261, 'HP:0025326', 'Retinal arterial occlusion', 'XPO:0130044', 'increased size of the hyaloid blood vessel', 0.45918367346938777, 10.24626555896271, 2.1690822618580805, 'UPHENO:0087915', 'abnormal vasculature of eye morphology'),
(106262, 'HP:0025326', 'Retinal arterial occlusion', 'XPO:0140754', 'abnormally necrotic optic choroid vascular plexus', 0.4722222222222222, 10.24626555896271, 2.1996623131136266, 'UPHENO:0087915', 'abnormal vasculature of eye morphology'),
(106263, 'HP:0025326', 'Retinal arterial occlusion', 'XPO:0139887', 'abnormally necrotic Muller cell', 0.41509433962264153, 8.767034997756374, 1.9076547388985956, 'UPHENO:0015314', 'abnormal anatomical entity morphology in the retina'),
(106264, 'HP:0025326', 'Retinal arterial occlusion', 'XPO:0127563', 'abnormally localised retinal blood vessel', 0.5368421052631579, 11.457162341461329, 2.4800578928186074, 'UPHENO:0005091', 'abnormal vasculature of retina'),
(106265, 'HP:0025326', 'Retinal arterial occlusion', 'XPO:0103186', 'abnormal peripheral retina morphology', 0.4583333333333333, 8.767034997756374, 2.004550915784299, 'UPHENO:0015314', 'abnormal anatomical entity morphology in the retina'),
(106266, 'HP:0025326', 'Retinal arterial occlusion', 'XPO:0125909', 'absent retinal blood vessel', 0.51, 11.457162341461329, 2.417261424452324, 'UPHENO:0005091', 'abnormal vasculature of retina'),
(106267, 'HP:0025326', 'Retinal arterial occlusion', 'XPO:0140487', 'abnormally necrotic retinal layer', 0.4536082474226804, 8.767034997756374, 1.9941914101774614, 'UPHENO:0015314', 'abnormal anatomical entity morphology in the retina'),
(106268, 'HP:0025326', 'Retinal arterial occlusion', 'XPO:0129780', 'increased size of the retina', 0.42574257425742573, 8.040873045973026, 1.850227550835222, 'HP:0000479', 'Abnormal retinal morphology'),
(106269, 'HP:0025326', 'Retinal arterial occlusion', 'XPO:0129810', 'increased size of the retinal progenitor cell region', 0.43137254901960786, 8.767034997756374, 1.9447000371075944, 'UPHENO:0015314', 'abnormal anatomical entity morphology in the retina'),
(106270, 'HP:0025326', 'Retinal arterial occlusion', 'XPO:0102342', 'abnormal hyaloid vein morphology', 0.4742268041237113, 10.24626555896271, 2.2043261487878194, 'UPHENO:0087915', 'abnormal vasculature of eye morphology'),
(106271, 'HP:0025326', 'Retinal arterial occlusion', 'XPO:0102441', 'abnormal retinal inner plexiform layer morphology', 0.411214953271028, 8.767034997756374, 1.898719538775502, 'UPHENO:0015314', 'abnormal anatomical entity morphology in the retina'),
(106272, 'HP:0025326', 'Retinal arterial occlusion', 'XPO:0130413', 'increased size of the central retina', 0.4489795918367347, 8.767034997756374, 1.9839908757126443, 'UPHENO:0015314', 'abnormal anatomical entity morphology in the retina'),
(106273, 'HP:0025326', 'Retinal arterial occlusion', 'XPO:0102663', 'abnormal retinal progenitor cell morphology', 0.41509433962264153, 8.767034997756374, 1.9076547388985956, 'UPHENO:0015314', 'abnormal anatomical entity morphology in the retina'),
(106274, 'HP:0025326', 'Retinal arterial occlusion', 'XPO:0140346', 'abnormally necrotic retinal blood vessel', 0.6262626262626263, 12.189682030596343, 2.76295897215062, 'UPHENO:0087970', 'abnormal retina blood vessel morphology'),
(106275, 'HP:0025326', 'Retinal arterial occlusion', 'XPO:0128779', 'decreased size of the retinal blood vessel', 0.6138613861386139, 12.189682030596343, 2.735466159156575, 'UPHENO:0087970', 'abnormal retina blood vessel morphology'),
(106276, 'HP:0025326', 'Retinal arterial occlusion', 'XPO:0100710', 'abnormal hyaloid vein', 0.42528735632183906, 9.463856994035337, 2.0062050547242762, 'UPHENO:0005090', 'abnormal vasculature of eye'),
(106277, 'HP:0025326', 'Retinal arterial occlusion', 'XPO:0102996', 'abnormal optic fiber layer morphology', 0.411214953271028, 8.767034997756374, 1.898719538775502, 'UPHENO:0015314', 'abnormal anatomical entity morphology in the retina'),
(106278, 'HP:0025326', 'Retinal arterial occlusion', 'XPO:0139722', 'abnormally necrotic hyaloid blood vessel', 0.46875, 10.24626555896271, 2.191560398611859, 'UPHENO:0087915', 'abnormal vasculature of eye morphology'),
(106279, 'HP:0025326', 'Retinal arterial occlusion', 'XPO:0103184', 'abnormal inner limiting membrane morphology', 0.411214953271028, 8.767034997756374, 1.898719538775502, 'UPHENO:0015314', 'abnormal anatomical entity morphology in the retina'),
(106280, 'HP:0025326', 'Retinal arterial occlusion', 'XPO:0102239', 'abnormal retinal pigmented epithelium morphology', 0.411214953271028, 8.767034997756374, 1.898719538775502, 'UPHENO:0015314', 'abnormal anatomical entity morphology in the retina'),
(106281, 'HP:0025326', 'Retinal arterial occlusion', 'XPO:0102003', 'abnormal hyaloid blood vessel morphology', 0.5, 10.24626555896271, 2.2634338469417115, 'UPHENO:0087915', 'abnormal vasculature of eye morphology'),
(106282, 'HP:0025326', 'Retinal arterial occlusion', 'XPO:0130829', 'increased size of the hyaloid vascular plexus', 0.4166666666666667, 10.24626555896271, 2.0662229589844516, 'UPHENO:0087915', 'abnormal vasculature of eye morphology'),
(106283, 'HP:0025326', 'Retinal arterial occlusion', 'XPO:0101861', 'abnormal photoreceptor layer morphology', 0.41509433962264153, 8.767034997756374, 1.9076547388985956, 'UPHENO:0015314', 'abnormal anatomical entity morphology in the retina'),
(106284, 'HP:0025326', 'Retinal arterial occlusion', 'XPO:0102805', 'abnormal retinal layer morphology', 0.4835164835164835, 8.767034997756374, 2.0588846332374002, 'UPHENO:0015314', 'abnormal anatomical entity morphology in the retina'),
(106285, 'HP:0025326', 'Retinal arterial occlusion', 'XPO:0102784', 'abnormal retinal progenitor cell region morphology', 0.4536082474226804, 8.767034997756374, 1.9941914101774614, 'UPHENO:0015314', 'abnormal anatomical entity morphology in the retina'),
(106286, 'HP:0025326', 'Retinal arterial occlusion', 'XPO:0141253', 'abnormally necrotic hyaloid vein', 0.4380952380952381, 10.24626555896271, 2.1186883087516213, 'UPHENO:0087915', 'abnormal vasculature of eye morphology'),
(106287, 'HP:0025326', 'Retinal arterial occlusion', 'XPO:0128787', 'decreased size of the peripheral retina', 0.4230769230769231, 8.767034997756374, 1.925910224117019, 'UPHENO:0015314', 'abnormal anatomical entity morphology in the retina'),
(106288, 'HP:0025326', 'Retinal arterial occlusion', 'XPO:0101961', 'abnormal retinal blood vessel morphology', 0.6739130434782609, 12.189682030596343, 2.8661447479622253, 'UPHENO:0087970', 'abnormal retina blood vessel morphology'),
(106289, 'HP:0025326', 'Retinal arterial occlusion', 'XPO:0103226', 'abnormal retinal outer plexiform layer morphology', 0.411214953271028, 8.767034997756374, 1.898719538775502, 'UPHENO:0015314', 'abnormal anatomical entity morphology in the retina'),
(106290, 'HP:0025326', 'Retinal arterial occlusion', 'XPO:0130522', 'increased size of the hyaloid vein', 0.42990654205607476, 10.24626555896271, 2.0987940812385366, 'UPHENO:0087915', 'abnormal vasculature of eye morphology'),
(106291, 'HP:0025326', 'Retinal arterial occlusion', 'XPO:0140553', 'abnormally necrotic retinal stem cell region', 0.44, 8.767034997756374, 1.9640507628401067, 'UPHENO:0015314', 'abnormal anatomical entity morphology in the retina'),
(106292, 'HP:0025326', 'Retinal arterial occlusion', 'XPO:0102017', 'abnormal retinal neural layer morphology', 0.41509433962264153, 8.767034997756374, 1.9076547388985956, 'UPHENO:0015314', 'abnormal anatomical entity morphology in the retina'),
(106293, 'HP:0025326', 'Retinal arterial occlusion', 'XPO:0100779', 'abnormal optic choroid vascular plexus', 0.43023255813953487, 9.463856994035337, 2.017835326385816, 'UPHENO:0005090', 'abnormal vasculature of eye'),
(106294, 'HP:0025326', 'Retinal arterial occlusion', 'XPO:0101359', 'abnormal hyaloid artery', 0.422680412371134, 9.463856994035337, 2.0000467436688316, 'UPHENO:0005090', 'abnormal vasculature of eye'),
(106295, 'HP:0025326', 'Retinal arterial occlusion', 'XPO:0102162', 'abnormal ciliary marginal zone morphology', 0.43564356435643564, 8.767034997756374, 1.9543035524862054, 'UPHENO:0015314', 'abnormal anatomical entity morphology in the retina'),
(106296, 'HP:0025326', 'Retinal arterial occlusion', 'XPO:0140161', 'abnormally necrotic hyaloid vascular plexus', 0.42452830188679247, 10.24626555896271, 2.0856245391794674, 'UPHENO:0087915', 'abnormal vasculature of eye morphology'),
(106297, 'HP:0025326', 'Retinal arterial occlusion', 'XPO:0128935', 'decreased size of the central retina', 0.4489795918367347, 8.767034997756374, 1.9839908757126443, 'UPHENO:0015314', 'abnormal anatomical entity morphology in the retina'),
(106298, 'HP:0004283', 'Narrow palm', 'XPO:0128741', 'decreased size of the interdigital region', 0.46938775510204084, 6.173473740856008, 1.7022787610734618, 'UPHENO:0087006', 'abnormal autopod region morphology'),
(106299, 'HP:0004283', 'Narrow palm', 'XPO:0103340', 'decreased size of the forelimb', 0.4166666666666667, 9.84136243681758, 2.02498584735976, 'UPHENO:0012274', 'decreased size of the anatomical entity in the pectoral complex'),
(106300, 'HP:0004283', 'Narrow palm', 'XPO:0128056', 'decreased size of the limb segment', 0.4074074074074074, 5.914846961127896, 1.5523377421311055, 'UPHENO:0084763', 'abnormal anatomical entity morphology in the appendage girdle complex'),
(106301, 'HP:0004283', 'Narrow palm', 'XPO:0130219', 'increased size of the interdigital region', 0.4117647058823529, 6.173473740856008, 1.5943709101636303, 'UPHENO:0087006', 'abnormal autopod region morphology'),
(106302, 'HP:0004283', 'Narrow palm', 'XPO:0102484', 'abnormal interdigital region morphology', 0.43478260869565216, 6.173473740856008, 1.6383281166370434, 'UPHENO:0087006', 'abnormal autopod region morphology'),
(106303, 'HP:0006498', 'Aplasia/Hypoplasia of the patella', 'XPO:0100178', 'abnormal digit', 0.4126984126984127, 5.802924133159483, 1.547532739157473, 'UPHENO:0076727', 'abnormal limb bone morphology'),
(106304, 'HP:0032043', 'Odynophagia', 'XPO:0101169', 'abnormal hepato-pancreatic duct', 0.4166666666666667, 5.05060299610679, 1.45066119926208, 'HP:0025031', 'Abnormality of the digestive system'),
(106305, 'HP:0032043', 'Odynophagia', 'XPO:0127393', 'abnormally localised pharyngeal cavity', 0.41025641025641024, 5.05060299610679, 1.4394590146346793, 'HP:0025031', 'Abnormality of the digestive system'),
(106306, 'HP:0032043', 'Odynophagia', 'XPO:0100156', 'abnormal foregut', 0.4411764705882353, 5.05060299610679, 1.4927180591674907, 'HP:0025031', 'Abnormality of the digestive system'),
(106307, 'HP:0032043', 'Odynophagia', 'XPO:0101198', 'abnormal digestive enzyme secreting cell', 0.40540540540540543, 5.05060299610679, 1.4309233924911664, 'HP:0025031', 'Abnormality of the digestive system'),
(106308, 'HP:0032043', 'Odynophagia', 'XPO:0101381', 'abnormal ventral foregut', 0.42857142857142855, 5.05060299610679, 1.471238981671103, 'HP:0025031', 'Abnormality of the digestive system'),
(106309, 'HP:0032043', 'Odynophagia', 'XPO:0142054', 'abnormal digestive tract', 0.45454545454545453, 5.05060299610679, 1.5151662069205463, 'HP:0025031', 'Abnormality of the digestive system'),
(106310, 'HP:0032043', 'Odynophagia', 'XPO:0100523', 'abnormal midgut', 0.4411764705882353, 5.05060299610679, 1.4927180591674907, 'HP:0025031', 'Abnormality of the digestive system'),
(106311, 'HP:0032043', 'Odynophagia', 'XPO:0101601', 'abnormal proctodeum', 0.4166666666666667, 5.05060299610679, 1.45066119926208, 'HP:0025031', 'Abnormality of the digestive system'),
(106312, 'HP:0032043', 'Odynophagia', 'XPO:0100462', 'abnormal anterior foregut', 0.42857142857142855, 5.05060299610679, 1.471238981671103, 'HP:0025031', 'Abnormality of the digestive system'),
(106313, 'HP:0032043', 'Odynophagia', 'XPO:0101332', 'abnormal left spleen primordium', 0.4146341463414634, 7.4630184615845945, 1.7590970095335021, 'UPHENO:0002725', 'abnormal alimentary part of gastrointestinal system'),
(106314, 'HP:0032043', 'Odynophagia', 'XPO:0115391', 'abnormally undifferentiated alimentary system', 0.46875, 5.05060299610679, 1.5386585568036393, 'HP:0025031', 'Abnormality of the digestive system'),
(106315, 'HP:0032043', 'Odynophagia', 'XPO:0100152', 'abnormal alimentary system', 0.4838709677419355, 5.05060299610679, 1.5632786569919361, 'HP:0025031', 'Abnormality of the digestive system'),
(106316, 'HP:0032043', 'Odynophagia', 'XPO:0101021', 'abnormal dorsal foregut', 0.42857142857142855, 5.05060299610679, 1.471238981671103, 'HP:0025031', 'Abnormality of the digestive system'),
(106317, 'HP:0032043', 'Odynophagia', 'XPO:0100486', 'abnormal oral evagination', 0.4411764705882353, 5.05060299610679, 1.4927180591674907, 'HP:0025031', 'Abnormality of the digestive system'),
(106318, 'HP:0032043', 'Odynophagia', 'XPO:0100492', 'abnormal gall bladder primordium', 0.40540540540540543, 5.05060299610679, 1.4309233924911664, 'HP:0025031', 'Abnormality of the digestive system'),
(106319, 'HP:0032043', 'Odynophagia', 'XPO:0100621', 'abnormal peritoneum', 0.40540540540540543, 5.05060299610679, 1.4309233924911664, 'HP:0025031', 'Abnormality of the digestive system'),
(106320, 'HP:0032043', 'Odynophagia', 'XPO:0101377', 'abnormal manicotto glandulare', 0.4411764705882353, 5.05060299610679, 1.4927180591674907, 'HP:0025031', 'Abnormality of the digestive system'),
(106321, 'HP:0032043', 'Odynophagia', 'XPO:0100735', 'abnormal hindgut', 0.4411764705882353, 5.05060299610679, 1.4927180591674907, 'HP:0025031', 'Abnormality of the digestive system'),
(106322, 'HP:0032043', 'Odynophagia', 'XPO:0100986', 'abnormal gut epithelium', 0.42857142857142855, 5.05060299610679, 1.471238981671103, 'HP:0025031', 'Abnormality of the digestive system'),
(106323, 'HP:0032043', 'Odynophagia', 'XPO:0107288', 'abnormal larval alimentary system', 0.46875, 5.05060299610679, 1.5386585568036393, 'HP:0025031', 'Abnormality of the digestive system'),
(106324, 'HP:0032043', 'Odynophagia', 'XPO:0100493', 'abnormal liver and biliary system', 0.46875, 5.05060299610679, 1.5386585568036393, 'HP:0025031', 'Abnormality of the digestive system'),
(106325, 'HP:0032043', 'Odynophagia', 'XPO:0100215', 'abnormal first pancreatic bud', 0.40540540540540543, 5.05060299610679, 1.4309233924911664, 'HP:0025031', 'Abnormality of the digestive system'),
(106326, 'HP:0032043', 'Odynophagia', 'XPO:0115495', 'abnormally protruding proctodeum', 0.42105263157894735, 5.05060299610679, 1.4582762710032966, 'HP:0025031', 'Abnormality of the digestive system'),
(106327, 'HP:0032043', 'Odynophagia', 'XPO:0126466', 'abnormally localised alimentary system', 0.41025641025641024, 5.05060299610679, 1.4394590146346793, 'HP:0025031', 'Abnormality of the digestive system'),
(106328, 'HP:0032043', 'Odynophagia', 'XPO:0100890', 'abnormal pharyngeal cavity', 0.45454545454545453, 5.05060299610679, 1.5151662069205463, 'HP:0025031', 'Abnormality of the digestive system'),
(106329, 'HP:0032043', 'Odynophagia', 'XPO:0107304', 'abnormal hindgut endoderm', 0.40540540540540543, 5.05060299610679, 1.4309233924911664, 'HP:0025031', 'Abnormality of the digestive system'),
(106330, 'HP:0032043', 'Odynophagia', 'XPO:0100718', 'abnormal ventral pancreatic bud', 0.4166666666666667, 5.05060299610679, 1.45066119926208, 'HP:0025031', 'Abnormality of the digestive system'),
(106331, 'HP:0032043', 'Odynophagia', 'XPO:0101101', 'abnormal posterior foregut', 0.42857142857142855, 5.05060299610679, 1.471238981671103, 'HP:0025031', 'Abnormality of the digestive system'),
(106332, 'HP:0010810', 'Long uvula', 'XPO:0103138', 'abnormal upper jaw morphology', 0.42857142857142855, 8.81758714901448, 1.9439562549106413, 'UPHENO:0087585', 'abnormal midface morphology'),
(106333, 'HP:0010810', 'Long uvula', 'XPO:0103199', 'abnormal tongue morphology', 0.5, 7.884497199543557, 1.9855096574360394, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(106334, 'HP:0010810', 'Long uvula', 'XPO:0126089', 'absent tongue', 0.4342105263157895, 7.884497199543557, 1.8502788110847448, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(106335, 'HP:0010810', 'Long uvula', 'XPO:0103096', 'abnormal oral cavity morphology', 0.5, 7.884497199543557, 1.9855096574360394, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(106336, 'HP:0010810', 'Long uvula', 'XPO:0140639', 'abnormally necrotic upper jaw', 0.4044943820224719, 8.81758714901448, 1.888561480272724, 'UPHENO:0087585', 'abnormal midface morphology'),
(106337, 'HP:0010810', 'Long uvula', 'XPO:0103735', 'increased size of the mouth', 0.5, 7.884497199543557, 1.9855096574360394, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(106338, 'HP:0010810', 'Long uvula', 'XPO:0102279', 'abnormal mouth morphology', 0.4714285714285714, 7.312692920701687, 1.856720866716972, 'UPHENO:0076800', 'abnormal mouth morphology'),
(106339, 'HP:0010810', 'Long uvula', 'XPO:0128105', 'decreased size of the tongue', 0.43902439024390244, 7.884497199543557, 1.8605070748076629, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(106340, 'HP:0010810', 'Long uvula', 'XPO:0115393', 'abnormally decreased volume of oral cavity', 0.47368421052631576, 7.884497199543557, 1.932553189788767, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(106341, 'HP:0010810', 'Long uvula', 'XPO:0141830', 'increased width of mouth', 0.4691358024691358, 7.884497199543557, 1.9232524329306127, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(106342, 'HP:0010810', 'Long uvula', 'XPO:0127750', 'abnormally localised tongue', 0.44594594594594594, 7.884497199543557, 1.8751158796081413, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(106343, 'HP:0010810', 'Long uvula', 'XPO:0140789', 'abnormally necrotic roof of mouth', 0.4230769230769231, 7.312692920701687, 1.7589291117884391, 'UPHENO:0076800', 'abnormal mouth morphology'),
(106344, 'HP:0010810', 'Long uvula', 'XPO:0129225', 'decreased size of the upper jaw', 0.4111111111111111, 8.81758714901448, 1.9039453905378687, 'UPHENO:0087585', 'abnormal midface morphology'),
(106345, 'HP:0010810', 'Long uvula', 'XPO:0129152', 'decreased size of the oral cavity', 0.4864864864864865, 7.884497199543557, 1.9584946618049506, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(106346, 'HP:0010810', 'Long uvula', 'XPO:0130132', 'increased size of the oral epithelium', 0.4235294117647059, 7.312692920701687, 1.7598694642275927, 'UPHENO:0076800', 'abnormal mouth morphology'),
(106347, 'HP:0010810', 'Long uvula', 'XPO:0130628', 'increased size of the oral cavity', 0.5277777777777778, 7.884497199543557, 2.0399172558881427, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(106348, 'HP:0010810', 'Long uvula', 'XPO:0130358', 'increased size of the lower jaw', 0.42045454545454547, 7.312692920701687, 1.7534694117726435, 'UPHENO:0076800', 'abnormal mouth morphology'),
(106349, 'HP:0010810', 'Long uvula', 'XPO:0129585', 'increased size of the tongue', 0.4470588235294118, 7.884497199543557, 1.8774541384941696, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(106350, 'HP:0010810', 'Long uvula', 'XPO:0115558', 'abnormally incomplete structure of mouth', 0.4647887323943662, 7.312692920701687, 1.8435990000545652, 'UPHENO:0076800', 'abnormal mouth morphology'),
(106351, 'HP:0010810', 'Long uvula', 'XPO:0101567', 'abnormal tongue', 0.5, 7.884497199543557, 1.9855096574360394, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(106352, 'HP:0010810', 'Long uvula', 'XPO:0141311', 'abnormal roof of mouth morphology', 0.4520547945205479, 7.312692920701687, 1.8181688303509294, 'UPHENO:0076800', 'abnormal mouth morphology'),
(106353, 'HP:0010810', 'Long uvula', 'XPO:0103352', 'decreased size of the mouth', 0.46153846153846156, 7.884497199543557, 1.907615974844424, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(106354, 'HP:0010810', 'Long uvula', 'XPO:0131611', 'increased size of the roof of mouth', 0.4675324675324675, 7.312692920701687, 1.84903254852987, 'UPHENO:0076800', 'abnormal mouth morphology'),
(106355, 'HP:0010810', 'Long uvula', 'XPO:0101659', 'abnormal lower jaw morphology', 0.40476190476190477, 7.312692920701687, 1.7204358504524693, 'UPHENO:0076800', 'abnormal mouth morphology'),
(106356, 'HP:0010810', 'Long uvula', 'XPO:0140626', 'abnormally necrotic tongue', 0.4666666666666667, 7.884497199543557, 1.9181845652735452, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(106357, 'HP:0010810', 'Long uvula', 'XPO:0102960', 'abnormal oral epithelium morphology', 0.4177215189873418, 7.312692920701687, 1.7477611949930372, 'UPHENO:0076800', 'abnormal mouth morphology'),
(106358, 'HP:0010810', 'Long uvula', 'XPO:0130701', 'increased size of the upper jaw', 0.4431818181818182, 8.81758714901448, 1.9768141806140687, 'UPHENO:0087585', 'abnormal midface morphology'),
(106359, 'HP:0010810', 'Long uvula', 'XPO:0131573', 'decreased size of the roof of mouth', 0.43037974683544306, 7.312692920701687, 1.7740447930920258, 'UPHENO:0076800', 'abnormal mouth morphology'),
(106360, 'HP:0010810', 'Long uvula', 'XPO:0103828', 'decreased width of the mouth', 0.43373493975903615, 7.884497199543557, 1.8492652372967795, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(106361, 'HP:0010574', 'Abnormality of the epiphysis of the femoral head', 'XPO:0102033', 'abnormal femur morphology', 0.40540540540540543, 10.819732420846037, 2.094368164495225, 'HP:0002823', 'Abnormal femur morphology'),
(106362, 'HP:0010574', 'Abnormality of the epiphysis of the femoral head', 'XPO:0141567', 'abnormal joint region morphology in the femur', 0.4019607843137255, 10.627087342903641, 2.06680244903184, 'UPHENO:0087558', 'abnormal femur morphology'),
(106363, 'HP:0011772', 'Abnormal thyroid morphology', 'XPO:0100872', 'abnormal neuroendocrine cell', 0.40625, 6.2194654996189955, 1.5895464319170476, 'UPHENO:0003116', 'abnormal endocrine system'),
(106364, 'HP:0011772', 'Abnormal thyroid morphology', 'XPO:0100840', 'abnormal thyroid', 0.4838709677419355, 10.665155383737162, 2.2716863904700872, 'UPHENO:0002689', 'abnormal thyroid gland'),
(106365, 'HP:0011772', 'Abnormal thyroid morphology', 'XPO:0129055', 'decreased size of the thyroid', 0.42857142857142855, 11.627087342903641, 2.2322718097653316, 'HP:0011772', 'Abnormal thyroid morphology'),
(106366, 'HP:0011772', 'Abnormal thyroid morphology', 'XPO:0102472', 'abnormal thyroid morphology', 0.525, 11.627087342903641, 2.470672146405591, 'HP:0011772', 'Abnormal thyroid morphology'),
(106367, 'HP:0011772', 'Abnormal thyroid morphology', 'XPO:0100225', 'abnormal endocrine system', 0.48148148148148145, 6.2194654996189955, 1.7304789691815143, 'UPHENO:0003116', 'abnormal endocrine system'),
(106368, 'HP:0011772', 'Abnormal thyroid morphology', 'XPO:0100004', 'abnormal cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(106369, 'HP:0011772', 'Abnormal thyroid morphology', 'XPO:0141659', 'neoplastic thyroid', 0.5, 11.627087342903641, 2.4111291279091254, 'HP:0011772', 'Abnormal thyroid morphology'),
(106370, 'HP:0011772', 'Abnormal thyroid morphology', 'XPO:0102492', 'abnormal parathyroid morphology', 0.43902439024390244, 7.767034997756375, 1.8465962752840814, 'UPHENO:0087376', 'abnormal endocrine gland morphology'),
(106371, 'HP:0011772', 'Abnormal thyroid morphology', 'XPO:0100189', 'abnormal enteroendocrine cell', 0.40625, 6.2194654996189955, 1.5895464319170476, 'UPHENO:0003116', 'abnormal endocrine system'),
(106372, 'HP:0011772', 'Abnormal thyroid morphology', 'XPO:0125918', 'absent thyroid', 0.42857142857142855, 11.627087342903641, 2.2322718097653316, 'HP:0011772', 'Abnormal thyroid morphology'),
(106373, 'HP:0011772', 'Abnormal thyroid morphology', 'XPO:0101857', 'abnormal endocrine system morphology', 0.47058823529411764, 7.428233084304616, 1.869662830163848, 'UPHENO:0076812', 'abnormal endocrine system morphology'),
(106374, 'HP:0011772', 'Abnormal thyroid morphology', 'XPO:0100860', 'abnormal parathyroid', 0.40625, 6.2194654996189955, 1.5895464319170476, 'UPHENO:0003116', 'abnormal endocrine system'),
(106375, 'HP:0011772', 'Abnormal thyroid morphology', 'XPO:0102655', 'abnormal ultimobranchial body morphology', 0.47368421052631576, 7.767034997756375, 1.9181037096680913, 'UPHENO:0087376', 'abnormal endocrine gland morphology'),
(106376, 'HP:0011772', 'Abnormal thyroid morphology', 'XPO:0101835', 'abnormal endocrine cell morphology', 0.41025641025641024, 7.428233084304616, 1.7457033653272007, 'UPHENO:0076812', 'abnormal endocrine system morphology'),
(106377, 'HP:0011772', 'Abnormal thyroid morphology', 'XPO:0140281', 'abnormally necrotic endocrine system', 0.41025641025641024, 7.428233084304616, 1.7457033653272007, 'UPHENO:0076812', 'abnormal endocrine system morphology'),
(106378, 'HP:0011772', 'Abnormal thyroid morphology', 'XPO:0140064', 'abnormally necrotic thyroid', 0.45652173913043476, 11.627087342903641, 2.30391365610863, 'HP:0011772', 'Abnormal thyroid morphology'),
(106379, 'HP:0011772', 'Abnormal thyroid morphology', 'XPO:0100203', 'abnormal endocrine cell', 0.41935483870967744, 6.2194654996189955, 1.6149807898093176, 'UPHENO:0003116', 'abnormal endocrine system'),
(106380, 'HP:0011772', 'Abnormal thyroid morphology', 'XPO:0101561', 'abnormal adrenal cortex', 0.4090909090909091, 7.767034997756375, 1.782532863139713, 'UPHENO:0087376', 'abnormal endocrine gland morphology'),
(106381, 'HP:0011772', 'Abnormal thyroid morphology', 'XPO:0139937', 'abnormally necrotic ultimobranchial body', 0.4186046511627907, 7.767034997756375, 1.803140864104908, 'UPHENO:0087376', 'abnormal endocrine gland morphology'),
(106382, 'HP:0011772', 'Abnormal thyroid morphology', 'XPO:0141629', 'metaplastic thyroid', 0.4411764705882353, 10.665155383737162, 2.1691508961970065, 'UPHENO:0002689', 'abnormal thyroid gland'),
(106383, 'HP:0011772', 'Abnormal thyroid morphology', 'XPO:0130532', 'increased size of the thyroid', 0.42, 11.627087342903641, 2.209836347791286, 'HP:0011772', 'Abnormal thyroid morphology'),
(106384, 'HP:0011772', 'Abnormal thyroid morphology', 'XPO:0101023', 'abnormal ultimobranchial body', 0.43333333333333335, 6.2194654996189955, 1.6416764956901726, 'UPHENO:0003116', 'abnormal endocrine system'),
(106385, 'HP:0006489', 'Abnormal femoral metaphysis morphology', 'XPO:0101810', 'abnormal digit morphology', 0.410958904109589, 5.914846961127896, 1.5590891652247003, 'UPHENO:0084763', 'abnormal anatomical entity morphology in the appendage girdle complex'),
(106386, 'HP:0006489', 'Abnormal femoral metaphysis morphology', 'XPO:0141567', 'abnormal joint region morphology in the femur', 0.43157894736842106, 10.627087342903641, 2.141594538899141, 'UPHENO:0087558', 'abnormal femur morphology'),
(106387, 'HP:0006489', 'Abnormal femoral metaphysis morphology', 'XPO:0102033', 'abnormal femur morphology', 0.4326923076923077, 10.819732420846037, 2.1637039977291606, 'HP:0002823', 'Abnormal femur morphology'),
(106388, 'HP:0006489', 'Abnormal femoral metaphysis morphology', 'XPO:0102880', 'abnormal digit-joint region morphology', 0.410958904109589, 5.914846961127896, 1.5590891652247003, 'UPHENO:0084763', 'abnormal anatomical entity morphology in the appendage girdle complex'),
(106389, 'HP:0006489', 'Abnormal femoral metaphysis morphology', 'XPO:0103008', 'abnormal iliac process morphology', 0.41379310344827586, 7.61213700143767, 1.7747816185937768, 'UPHENO:0079871', 'abnormal anatomical entity morphology in the skeleton of pelvic complex'),
(106390, 'HP:0006489', 'Abnormal femoral metaphysis morphology', 'XPO:0141562', 'abnormal femur morphology in the regenerating hindlimb', 0.41284403669724773, 10.819732420846037, 2.113495211398919, 'HP:0002823', 'Abnormal femur morphology'),
(106391, 'HP:0007534', 'Congenital posterior occipital alopecia', 'XPO:0102139', 'abnormal skin morphology', 0.42, 7.420886955069779, 1.7654383368244009, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(106392, 'HP:0007534', 'Congenital posterior occipital alopecia', 'XPO:0102615', 'abnormal skin gland morphology', 0.42, 7.420886955069779, 1.7654383368244009, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(106393, 'HP:0007534', 'Congenital posterior occipital alopecia', 'XPO:0102727', 'abnormal skin seromucous gland morphology', 0.40384615384615385, 7.420886955069779, 1.7311547172139254, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(106394, 'HP:0007534', 'Congenital posterior occipital alopecia', 'XPO:0102626', 'abnormal granular gland morphology', 0.40384615384615385, 7.420886955069779, 1.7311547172139254, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(106395, 'HP:0007534', 'Congenital posterior occipital alopecia', 'XPO:0102561', 'abnormal dermis morphology', 0.4117647058823529, 7.420886955069779, 1.7480444314835069, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(106396, 'HP:0032271', 'Extrapulmonary tuberculosis', 'XPO:0101029', 'abnormal right spleen primordium', 0.40625, 5.64885357140806, 1.5148751642906173, 'HP:0002715', 'Abnormality of the immune system'),
(106397, 'HP:0032271', 'Extrapulmonary tuberculosis', 'XPO:0100745', 'abnormal anterior lymph sac', 0.41935483870967744, 5.64885357140806, 1.5391147060347428, 'HP:0002715', 'Abnormality of the immune system'),
(106398, 'HP:0032271', 'Extrapulmonary tuberculosis', 'XPO:0100449', 'abnormal lymphocyte', 0.40625, 5.64885357140806, 1.5148751642906173, 'HP:0002715', 'Abnormality of the immune system'),
(106399, 'HP:0032271', 'Extrapulmonary tuberculosis', 'XPO:0101221', 'abnormal larval immune system', 0.4482758620689655, 5.64885357140806, 1.5913028324062968, 'HP:0002715', 'Abnormality of the immune system'),
(106400, 'HP:0032271', 'Extrapulmonary tuberculosis', 'XPO:0100599', 'abnormal adult immune system', 0.4482758620689655, 5.64885357140806, 1.5913028324062968, 'HP:0002715', 'Abnormality of the immune system'),
(106401, 'HP:0032271', 'Extrapulmonary tuberculosis', 'XPO:0100581', 'abnormal immune system', 0.4642857142857143, 5.64885357140806, 1.6194696710023933, 'HP:0002715', 'Abnormality of the immune system'),
(106402, 'HP:0032271', 'Extrapulmonary tuberculosis', 'XPO:0141497', 'abnormal lymphoblast', 0.40625, 5.64885357140806, 1.5148751642906173, 'HP:0002715', 'Abnormality of the immune system'),
(106403, 'HP:0032271', 'Extrapulmonary tuberculosis', 'XPO:0101451', 'abnormal dorsal lymph space', 0.43333333333333335, 5.64885357140806, 1.5645563421015427, 'HP:0002715', 'Abnormality of the immune system'),
(106404, 'HP:0032271', 'Extrapulmonary tuberculosis', 'XPO:0100232', 'abnormal lymphatic system', 0.4642857142857143, 5.64885357140806, 1.6194696710023933, 'HP:0002715', 'Abnormality of the immune system'),
(106405, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0100481', 'abnormal anatomical line', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(106406, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0100225', 'abnormal endocrine system', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(106407, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0100888', 'abnormal microtubule', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(106408, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0141315', 'abnormal anatomical region', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(106409, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0100501', 'abnormal urogenital system', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(106410, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0141263', 'abnormal visually guided collision avoidance behavior', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(106411, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0107259', 'abnormal animal-vegetal axis', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(106412, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0141852', 'abnormal glucose metabolic process', 0.4230769230769231, 4.758907843651163, 1.418937661667548, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(106413, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0100533', 'abnormal melanoblast', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(106414, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0101472', 'abnormal zygote cortex', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(106415, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0100307', 'abnormal blastomere', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(106416, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0141782', 'abnormal methylation', 0.5238095238095238, 4.758907843651163, 1.5788480773767701, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(106417, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0131694', 'abnormal RNA polymerase II activity', 0.4583333333333333, 4.758907843651163, 1.4768771428276568, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(106418, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0141880', 'abnormal ethanolamine metabolic process', 0.44, 4.758907843651163, 1.447038165082909, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(106419, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0115508', 'abnormally peramorphic growth of whole organism', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(106420, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0100289', 'abnormal chondroblast', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(106421, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0101132', 'abnormal apoptotic cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(106422, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0141859', 'abnormal lactose catabolic process', 0.4230769230769231, 4.758907843651163, 1.418937661667548, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(106423, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0101237', 'abnormal mucus secreting cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(106424, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0100032', 'abnormal nervous system', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(106425, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0107258', 'abnormal anatomical axis', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(106426, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0101333', 'abnormal barrier epithelial cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(106427, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0100429', 'abnormal spermatid', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(106428, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0141809', 'abnormal catalytic activity', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(106429, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0115512', 'abnormally semi-erect whole organism', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(106430, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0100108', 'abnormal cell part', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(106431, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0107260', 'abnormal anterior-posterior axis', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(106432, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0100285', 'abnormal progenitor cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(106433, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0141783', 'abnormal collagen metabolic process', 0.5238095238095238, 4.758907843651163, 1.5788480773767701, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(106434, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0141600', 'absent metamorphosis', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(106435, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0141877', 'abnormal 2-deoxyribose 1-phosphate metabolic process', 0.4583333333333333, 4.758907843651163, 1.4768771428276568, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(106436, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0100724', 'abnormal kinetochore', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(106437, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0101535', 'abnormal absorptive cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(106438, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0115505', 'dead whole organism', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(106439, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0141789', 'abnormal hormone catabolic process', 0.44, 4.758907843651163, 1.447038165082909, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(106440, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0131745', 'abnormal axis elongation', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(106441, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0100721', 'abnormal centromere', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(106442, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0101157', 'abnormal female organism', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(106443, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0131666', 'abnormal adherens junction', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(106444, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0100969', 'abnormal disaggregated/reaggregated ectoderm treated with activin', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(106445, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0101220', 'abnormal centriole', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(106446, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0100025', 'abnormal oocyte', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(106447, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0100573', 'abnormal extraembryonic structure', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(106448, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0101467', 'abnormal alkali secreting cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(106449, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0131723', 'abnormal pathway-restricted SMAD protein phosphorylation', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(106450, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0128000', 'absent behavior', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(106451, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0141892', 'abnormal inositol metabolic process', 0.4782608695652174, 4.758907843651163, 1.508641575552437, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(106452, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0100010', 'abnormal multicellular anatomical structure', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(106453, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0100176', 'abnormal stage VI oocyte', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(106454, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0141770', 'abnormal urate homeostasis', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(106455, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0101373', 'abnormal oxygen accumulating cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(106456, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0116494', 'absent biological process', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(106457, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0141784', 'abnormal cellular hormone metabolic process', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(106458, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0141864', 'abnormal 5-methylcytosine metabolic process', 0.4230769230769231, 4.758907843651163, 1.418937661667548, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(106459, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0100372', 'abnormal hematological system', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(106460, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0141738', 'abnormal carbon dioxide homeostasis', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(106461, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0141883', 'abnormal glycerol metabolic process', 0.4230769230769231, 4.758907843651163, 1.418937661667548, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(106462, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0100902', 'abnormal spermatocyte', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(106463, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0141767', 'abnormal temperature homeostasis', 0.44, 4.758907843651163, 1.447038165082909, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(106464, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0141908', 'abnormal pyridine metabolic process', 0.4230769230769231, 4.758907843651163, 1.418937661667548, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(106465, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0107270', 'abnormal proximal-distal axis', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(106466, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0141786', 'abnormal pigment metabolic process', 0.5238095238095238, 4.758907843651163, 1.5788480773767701, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(106467, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0141910', 'abnormal D-ribose metabolic process', 0.4230769230769231, 4.758907843651163, 1.418937661667548, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(106468, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0100437', 'abnormal proepicardium', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(106469, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0100626', 'abnormal primordial germ cell', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(106470, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0141790', 'abnormal cellular metabolic process', 0.5, 4.758907843651163, 1.5425478669479211, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(106471, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0101326', 'abnormal cementoblast', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(106472, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0141860', 'abnormal malate-aspartate shuttle', 0.5, 4.758907843651163, 1.5425478669479211, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(106473, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0101241', 'abnormal nucleate erythrocyte', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(106474, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0100599', 'abnormal adult immune system', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(106475, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0131469', 'abnormal heart process', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(106476, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0141754', 'abnormal homeostatic process', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(106477, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0100581', 'abnormal immune system', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(106478, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0100062', 'abnormal anatomical space', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(106479, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0131729', 'abnormal regulation of growth rate', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(106480, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0100802', 'abnormal exocrine cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(106481, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0141266', 'abnormal surface breathing', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(106482, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0131685', 'abnormal cortical actin cytoskeleton', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(106483, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0107261', 'abnormal dorsal-ventral axis', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(106484, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0131725', 'abnormal phosphorylation of RNA polymerase II C-terminal domain', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(106485, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0141781', 'abnormal secondary metabolic process', 0.5238095238095238, 4.758907843651163, 1.5788480773767701, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(106486, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0101480', 'abnormal stage V oocyte', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(106487, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0107253', 'abnormal enteric nervous system', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(106488, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0100377', 'abnormal connective tissue', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(106489, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0133403', 'abnormal developmental process', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(106490, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0100791', 'abnormal multiciliated cell precursor', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(106491, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0101435', 'abnormal paracrine cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(106492, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0141881', 'abnormal fructose metabolic process', 0.4230769230769231, 4.758907843651163, 1.418937661667548, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(106493, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0100704', 'abnormal Merkel cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(106494, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0100258', 'abnormal organ part', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(106495, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0100172', 'abnormal stem cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(106496, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0100549', 'abnormal mitotic cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(106497, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0131675', 'abnormal spindle microtubule', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(106498, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0141499', 'abnormal tadpole', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(106499, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0115509', 'abnormally semi-viable whole organism', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(106500, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0141743', 'abnormal chemical homeostasis within a tissue', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(106501, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0101004', 'abnormal acid secreting cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(106502, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0100907', 'abnormal cytoplasm', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(106503, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0141272', 'absent surface breathing', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(106504, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0107312', 'abnormal filopodium', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(106505, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0141745', 'abnormal creatinine homeostasis', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(106506, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0100386', 'abnormal limb', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(106507, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0100084', 'abnormal anatomical group', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(106508, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0141264', 'abnormal schooling behavior', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(106509, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0100423', 'abnormal process', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(106510, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0100006', 'abnormal anatomical structure', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(106511, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0100515', 'abnormal somatic stem cell', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(106512, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0101228', 'abnormal mesenchymal stem cell', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(106513, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0141276', 'decreased surface breathing', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(106514, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0100956', 'abnormal centrosome', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(106515, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0141796', 'abnormal demethylation', 0.5238095238095238, 4.758907843651163, 1.5788480773767701, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(106516, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0100728', 'abnormal cell condensation', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(106517, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0100232', 'abnormal lymphatic system', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(106518, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0141267', 'abnormal resting posture', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(106519, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0101366', 'abnormal morula cell', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(106520, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0100899', 'abnormal secondary spermatogonium', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(106521, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0101141', 'abnormal Keller explant', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(106522, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0141898', 'abnormal maltose metabolic process', 0.4583333333333333, 4.758907843651163, 1.4768771428276568, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(106523, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0100274', 'abnormal sensory system', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(106524, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0100754', 'abnormal electrically active cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(106525, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0100574', 'abnormal gastrula cell', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(106526, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0116434', 'abnormal biological process', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(106527, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0141788', 'abnormal hormone biosynthetic process', 0.44, 4.758907843651163, 1.447038165082909, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(106528, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0141794', 'abnormal prosthetic group metabolic process', 0.5238095238095238, 4.758907843651163, 1.5788480773767701, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(106529, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0101297', 'abnormal barrier cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(106530, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0100477', 'abnormal pericyte', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(106531, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0141772', 'abnormal water homeostasis', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(106532, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0133388', 'absent insulin receptor signaling pathway', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(106533, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0141884', 'abnormal phosphagen metabolic process', 0.4230769230769231, 4.758907843651163, 1.418937661667548, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(106534, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0100031', 'abnormal central nervous system', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(106535, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0141850', 'abnormal galactose metabolic process', 0.4230769230769231, 4.758907843651163, 1.418937661667548, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(106536, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0100715', 'abnormal ciliated cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(106537, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0101109', 'abnormal egg cell-free extract', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(106538, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0100317', 'abnormal respiratory system', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(106539, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0101061', 'abnormal plasma membrane', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(106540, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0100917', 'abnormal stage III oocyte', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(106541, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0100239', 'abnormal acellular anatomical structure', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(106542, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0131677', 'abnormal actin filament', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(106543, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0131667', 'abnormal actin cytoskeleton', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(106544, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0100392', 'abnormal cilium', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(106545, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0101468', 'abnormal stage I oocyte', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(106546, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0101498', 'abnormal stage II oocyte', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(106547, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0141903', 'abnormal inositol phosphate metabolic process', 0.4230769230769231, 4.758907843651163, 1.418937661667548, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(106548, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0100081', 'abnormal anatomical entity in vitro', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(106549, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0100546', 'abnormal whole organism', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(106550, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0107284', 'abnormal migrating myoblast', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(106551, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0141792', 'abnormal small molecule metabolic process', 0.5238095238095238, 4.758907843651163, 1.5788480773767701, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(106552, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0141787', 'abnormal hormone metabolic process', 0.5238095238095238, 4.758907843651163, 1.5788480773767701, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(106553, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0100026', 'abnormal germ cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(106554, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0101240', 'abnormal ciliated non-epidermal cell', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(106555, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0141777', 'abnormal catabolic process', 0.5238095238095238, 4.758907843651163, 1.5788480773767701, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(106556, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0141798', 'abnormal lipid metabolic process', 0.4782608695652174, 4.758907843651163, 1.508641575552437, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(106557, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0141776', 'abnormal metabolic process', 0.5789473684210527, 4.758907843651163, 1.6598666129060333, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(106558, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0101071', 'abnormal endoplasmic reticulum', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(106559, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0100344', 'abnormal portion of organism substance', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(106560, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0100976', 'abnormal multiciliated cell', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(106561, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0142057', 'abnormal desmosome', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(106562, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0141904', 'abnormal glucosamine metabolic process', 0.5238095238095238, 4.758907843651163, 1.5788480773767701, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(106563, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0101409', 'abnormal perivitelline space', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(106564, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0101110', 'abnormal cell-free extract', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(106565, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0101448', 'abnormal myelin accumulating cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(106566, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0141748', 'abnormal gas homeostasis', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(106567, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0100653', 'abnormal myoblast', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(106568, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0100674', 'abnormal secondary oogonium', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(106569, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0141771', 'abnormal urea homeostasis', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(106570, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0100004', 'abnormal cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(106571, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0100545', 'abnormal male organism', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(106572, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0100894', 'abnormal nucleus', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(106573, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0101461', 'abnormal sperm entry point', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(106574, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0100202', 'abnormal embryo', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(106575, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0100337', 'abnormal zygote', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(106576, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0100585', 'abnormal elastica externa', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(106577, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0141854', 'abnormal glutathione metabolic process', 0.4230769230769231, 4.758907843651163, 1.418937661667548, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(106578, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0101264', 'abnormal mitotic spindle', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(106579, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0141778', 'abnormal biosynthetic process', 0.5238095238095238, 4.758907843651163, 1.5788480773767701, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(106580, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0141900', 'abnormal mannose metabolic process', 0.4230769230769231, 4.758907843651163, 1.418937661667548, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(106581, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0141907', 'abnormal putrescine metabolic process', 0.4782608695652174, 4.758907843651163, 1.508641575552437, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(106582, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0100638', 'abnormal polar body', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(106583, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0141795', 'abnormal glycosylation', 0.4782608695652174, 4.758907843651163, 1.508641575552437, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(106584, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0101221', 'abnormal larval immune system', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(106585, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0100852', 'abnormal interdigital region', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(106586, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0100691', 'abnormal keratin accumulating cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(106587, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0141866', 'abnormal dicarboxylic acid metabolic process', 0.4074074074074074, 4.758907843651163, 1.392413123563799, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(106588, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0100308', 'abnormal early embryonic cell', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(106589, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0141791', 'abnormal primary metabolic process', 0.5238095238095238, 4.758907843651163, 1.5788480773767701, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(106590, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0131730', 'abnormal regulation of protein folding', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(106591, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0141911', 'abnormal ribose phosphate metabolic process', 0.4583333333333333, 4.758907843651163, 1.4768771428276568, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(106592, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0141797', 'abnormal hydrogen metabolic process', 0.5238095238095238, 4.758907843651163, 1.5788480773767701, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(106593, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0141872', 'abnormal cholesterol metabolic process', 0.4074074074074074, 4.758907843651163, 1.392413123563799, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(106594, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0101113', 'abnormal stage IV oocyte', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(106595, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0107262', 'abnormal left-right axis', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(106596, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0131691', 'abnormal molecular function', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(106597, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0101513', 'abnormal basal body', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(106598, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:00000000', 'Xenopus phenotype', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(106599, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0141265', 'abnormal escape behavior', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(106600, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0141271', 'increased surface breathing', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(106601, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0101547', 'abnormal lampbrush chromosome', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(106602, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0141775', 'abnormal nitrogen compound metabolic process', 0.5238095238095238, 4.758907843651163, 1.5788480773767701, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(106603, 'HP:0003649', 'Abnormality of glycoside metabolism', 'XPO:0101569', 'abnormal activin-induced ectoderm', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(106604, 'HP:0000219', 'Thin upper lip vermilion', 'XPO:0101567', 'abnormal tongue', 0.5079365079365079, 7.884497199543557, 2.0012056302067838, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(106605, 'HP:0000219', 'Thin upper lip vermilion', 'XPO:0127750', 'abnormally localised tongue', 0.4520547945205479, 7.884497199543557, 1.8879154539961525, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(106606, 'HP:0000219', 'Thin upper lip vermilion', 'XPO:0128653', 'decreased size of the oral epithelium', 0.42857142857142855, 7.312692920701687, 1.7703138850862843, 'UPHENO:0076800', 'abnormal mouth morphology'),
(106607, 'HP:0000219', 'Thin upper lip vermilion', 'XPO:0140639', 'abnormally necrotic upper jaw', 0.4090909090909091, 8.81758714901448, 1.8992616309446815, 'UPHENO:0087585', 'abnormal midface morphology'),
(106608, 'HP:0000219', 'Thin upper lip vermilion', 'XPO:0129585', 'increased size of the tongue', 0.4186046511627907, 7.884497199543557, 1.816724304843454, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(106609, 'HP:0000219', 'Thin upper lip vermilion', 'XPO:0103357', 'decreased size of the pharyngeal arch', 0.40540540540540543, 5.725717590856133, 1.5235605866383823, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(106610, 'HP:0000219', 'Thin upper lip vermilion', 'XPO:0103138', 'abnormal upper jaw morphology', 0.43373493975903615, 8.81758714901448, 1.9556317728288848, 'UPHENO:0087585', 'abnormal midface morphology'),
(106611, 'HP:0000219', 'Thin upper lip vermilion', 'XPO:0103199', 'abnormal tongue morphology', 0.5072463768115942, 7.884497199543557, 1.99984565340669, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(106612, 'HP:0000219', 'Thin upper lip vermilion', 'XPO:0130701', 'increased size of the upper jaw', 0.4157303370786517, 8.81758714901448, 1.9146118347279109, 'UPHENO:0087585', 'abnormal midface morphology'),
(106613, 'HP:0000219', 'Thin upper lip vermilion', 'XPO:0141311', 'abnormal roof of mouth morphology', 0.4583333333333333, 7.312692920701687, 1.830751463740579, 'UPHENO:0076800', 'abnormal mouth morphology'),
(106614, 'HP:0000219', 'Thin upper lip vermilion', 'XPO:0129225', 'decreased size of the upper jaw', 0.4482758620689655, 8.81758714901448, 1.988142721384131, 'UPHENO:0087585', 'abnormal midface morphology'),
(106615, 'HP:0000219', 'Thin upper lip vermilion', 'XPO:0126089', 'absent tongue', 0.44, 7.884497199543557, 1.8625731577039237, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(106616, 'HP:0000219', 'Thin upper lip vermilion', 'XPO:0140626', 'abnormally necrotic tongue', 0.47297297297297297, 7.884497199543557, 1.9311017790021312, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(106617, 'HP:0000219', 'Thin upper lip vermilion', 'XPO:0103096', 'abnormal oral cavity morphology', 0.5072463768115942, 7.884497199543557, 1.99984565340669, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(106618, 'HP:0000219', 'Thin upper lip vermilion', 'XPO:0140789', 'abnormally necrotic roof of mouth', 0.42857142857142855, 7.312692920701687, 1.7703138850862843, 'UPHENO:0076800', 'abnormal mouth morphology'),
(106619, 'HP:0000219', 'Thin upper lip vermilion', 'XPO:0115393', 'abnormally decreased volume of oral cavity', 0.5205479452054794, 7.884497199543557, 2.0258970398815324, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(106620, 'HP:0000219', 'Thin upper lip vermilion', 'XPO:0131573', 'decreased size of the roof of mouth', 0.47368421052631576, 7.312692920701687, 1.8611574820428165, 'UPHENO:0076800', 'abnormal mouth morphology'),
(106621, 'HP:0000219', 'Thin upper lip vermilion', 'XPO:0115558', 'abnormally incomplete structure of mouth', 0.4714285714285714, 7.312692920701687, 1.856720866716972, 'UPHENO:0076800', 'abnormal mouth morphology'),
(106622, 'HP:0000219', 'Thin upper lip vermilion', 'XPO:0128105', 'decreased size of the tongue', 0.4810126582278481, 7.884497199543557, 1.9474452384450944, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(106623, 'HP:0000219', 'Thin upper lip vermilion', 'XPO:0131611', 'increased size of the roof of mouth', 0.4358974358974359, 7.312692920701687, 1.7853806579100147, 'UPHENO:0076800', 'abnormal mouth morphology'),
(106624, 'HP:0000219', 'Thin upper lip vermilion', 'XPO:0103352', 'decreased size of the mouth', 0.5066666666666667, 7.884497199543557, 1.9987025577697655, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(106625, 'HP:0000219', 'Thin upper lip vermilion', 'XPO:0101659', 'abnormal lower jaw morphology', 0.40963855421686746, 7.312692920701687, 1.7307688914087174, 'UPHENO:0076800', 'abnormal mouth morphology'),
(106626, 'HP:0000219', 'Thin upper lip vermilion', 'XPO:0103735', 'increased size of the mouth', 0.4675324675324675, 7.884497199543557, 1.919963132707352, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(106627, 'HP:0000219', 'Thin upper lip vermilion', 'XPO:0103828', 'decreased width of the mouth', 0.475, 7.884497199543557, 1.9352354300661172, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(106628, 'HP:0000219', 'Thin upper lip vermilion', 'XPO:0141830', 'increased width of mouth', 0.43902439024390244, 7.884497199543557, 1.8605070748076629, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(106629, 'HP:0000219', 'Thin upper lip vermilion', 'XPO:0128880', 'decreased size of the lower jaw', 0.42528735632183906, 7.312692920701687, 1.7635180293489057, 'UPHENO:0076800', 'abnormal mouth morphology'),
(106630, 'HP:0000219', 'Thin upper lip vermilion', 'XPO:0130628', 'increased size of the oral cavity', 0.4931506849315068, 7.884497199543557, 1.9718633812451238, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(106631, 'HP:0000219', 'Thin upper lip vermilion', 'XPO:0102279', 'abnormal mouth morphology', 0.4782608695652174, 7.312692920701687, 1.8701269676463677, 'UPHENO:0076800', 'abnormal mouth morphology'),
(106632, 'HP:0000219', 'Thin upper lip vermilion', 'XPO:0129152', 'decreased size of the oral cavity', 0.5352112676056338, 7.884497199543557, 2.0542326403308797, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(106633, 'HP:0000219', 'Thin upper lip vermilion', 'XPO:0102960', 'abnormal oral epithelium morphology', 0.4230769230769231, 7.312692920701687, 1.7589291117884391, 'UPHENO:0076800', 'abnormal mouth morphology'),
(106634, 'HP:0001407', 'Hepatic cysts', 'XPO:0140908', 'abnormally necrotic hepatocyte', 0.4520547945205479, 9.184143847054914, 2.0375809823483246, 'UPHENO:0086622', 'abnormal liver morphology'),
(106635, 'HP:0001407', 'Hepatic cysts', 'XPO:0129330', 'decreased size of the biliary tree', 0.4153846153846154, 8.69832224767236, 1.900828567057226, 'UPHENO:0087100', 'abnormal hepatobiliary system morphology'),
(106636, 'HP:0001407', 'Hepatic cysts', 'XPO:0129120', 'decreased size of the hepatic vein', 0.40229885057471265, 10.01729298920255, 2.0074724046487695, 'UPHENO:0019492', 'abnormal liver morphology'),
(106637, 'HP:0001407', 'Hepatic cysts', 'XPO:0102653', 'abnormal dorsal foregut morphology', 0.40384615384615385, 5.725717590856133, 1.520627839767678, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(106638, 'HP:0001407', 'Hepatic cysts', 'XPO:0129858', 'increased size of the hepatic portal vein', 0.40229885057471265, 10.01729298920255, 2.0074724046487695, 'UPHENO:0019492', 'abnormal liver morphology'),
(106639, 'HP:0001407', 'Hepatic cysts', 'XPO:0107375', 'abnormal larval alimentary system morphology', 0.42857142857142855, 5.725717590856133, 1.5664861849086864, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(106640, 'HP:0001407', 'Hepatic cysts', 'XPO:0102655', 'abnormal ultimobranchial body morphology', 0.4117647058823529, 7.767034997756375, 1.7883486464974037, 'UPHENO:0087376', 'abnormal endocrine gland morphology'),
(106641, 'HP:0001407', 'Hepatic cysts', 'XPO:0128378', 'decreased size of the hepatic portal vein', 0.40229885057471265, 10.01729298920255, 2.0074724046487695, 'UPHENO:0019492', 'abnormal liver morphology'),
(106642, 'HP:0001407', 'Hepatic cysts', 'XPO:0141647', 'neoplastic liver', 0.5223880597014925, 10.01729298920255, 2.287556392330227, 'UPHENO:0019492', 'abnormal liver morphology'),
(106643, 'HP:0001407', 'Hepatic cysts', 'XPO:0129821', 'increased size of the pharyngeal cavity', 0.40384615384615385, 5.725717590856133, 1.520627839767678, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(106644, 'HP:0001407', 'Hepatic cysts', 'XPO:0141005', 'abnormally necrotic bile duct', 0.4153846153846154, 8.69832224767236, 1.900828567057226, 'UPHENO:0087100', 'abnormal hepatobiliary system morphology'),
(106645, 'HP:0001407', 'Hepatic cysts', 'XPO:0102211', 'abnormal biliary tree morphology', 0.46551724137931033, 8.69832224767236, 2.012267123759845, 'UPHENO:0087100', 'abnormal hepatobiliary system morphology'),
(106646, 'HP:0001407', 'Hepatic cysts', 'XPO:0125433', 'absent hepatic vein', 0.47297297297297297, 10.01729298920255, 2.176673803362472, 'UPHENO:0019492', 'abnormal liver morphology'),
(106647, 'HP:0001407', 'Hepatic cysts', 'XPO:0101820', 'abnormal delta cell morphology', 0.43859649122807015, 7.428233084304616, 1.8049922345540077, 'UPHENO:0076812', 'abnormal endocrine system morphology'),
(106648, 'HP:0001407', 'Hepatic cysts', 'XPO:0140793', 'abnormally necrotic hepatic portal vein', 0.4117647058823529, 10.01729298920255, 2.0309524124007297, 'UPHENO:0019492', 'abnormal liver morphology'),
(106649, 'HP:0001407', 'Hepatic cysts', 'XPO:0129248', 'decreased size of the liver parenchyme', 0.49295774647887325, 10.01729298920255, 2.2221841007837098, 'UPHENO:0019492', 'abnormal liver morphology'),
(106650, 'HP:0001407', 'Hepatic cysts', 'XPO:0103088', 'abnormal capillary system of liver morphology', 0.4125, 9.184143847054914, 1.9463965004361654, 'UPHENO:0086622', 'abnormal liver morphology'),
(106651, 'HP:0001407', 'Hepatic cysts', 'XPO:0101787', 'abnormal hepatic portal vein morphology', 0.44871794871794873, 10.01729298920255, 2.1201271569935747, 'UPHENO:0019492', 'abnormal liver morphology'),
(106652, 'HP:0001407', 'Hepatic cysts', 'XPO:0128672', 'decreased size of the liver', 0.44871794871794873, 10.01729298920255, 2.1201271569935747, 'UPHENO:0019492', 'abnormal liver morphology'),
(106653, 'HP:0001407', 'Hepatic cysts', 'XPO:0103009', 'abnormal manicotto glandulare morphology', 0.42, 5.725717590856133, 1.5507422055775666, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(106654, 'HP:0001407', 'Hepatic cysts', 'XPO:0102763', 'abnormal hepatocyte morphology', 0.4852941176470588, 9.184143847054914, 2.111163419681238, 'UPHENO:0086622', 'abnormal liver morphology'),
(106655, 'HP:0001407', 'Hepatic cysts', 'XPO:0102094', 'abnormal anterior foregut morphology', 0.40384615384615385, 5.725717590856133, 1.520627839767678, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(106656, 'HP:0001407', 'Hepatic cysts', 'XPO:0126004', 'absent hepatic portal vein', 0.4117647058823529, 10.01729298920255, 2.0309524124007297, 'UPHENO:0019492', 'abnormal liver morphology'),
(106657, 'HP:0001407', 'Hepatic cysts', 'XPO:0139877', 'abnormally necrotic liver', 0.4666666666666667, 10.01729298920255, 2.162113948961646, 'UPHENO:0019492', 'abnormal liver morphology'),
(106658, 'HP:0001407', 'Hepatic cysts', 'XPO:0103013', 'abnormal ventral foregut morphology', 0.40384615384615385, 5.725717590856133, 1.520627839767678, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(106659, 'HP:0001407', 'Hepatic cysts', 'XPO:0101788', 'abnormal foregut morphology', 0.4117647058823529, 5.725717590856133, 1.5354635846428564, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(106660, 'HP:0001407', 'Hepatic cysts', 'XPO:0129280', 'decreased size of the hepatocyte', 0.4074074074074074, 9.184143847054914, 1.9343443938413178, 'UPHENO:0086622', 'abnormal liver morphology'),
(106661, 'HP:0001407', 'Hepatic cysts', 'XPO:0128341', 'decreased size of the pharyngeal cavity', 0.40384615384615385, 5.725717590856133, 1.520627839767678, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(106662, 'HP:0001407', 'Hepatic cysts', 'XPO:0102618', 'abnormal gut epithelium morphology', 0.40384615384615385, 5.725717590856133, 1.520627839767678, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(106663, 'HP:0001407', 'Hepatic cysts', 'XPO:0102367', 'abnormal hindgut morphology', 0.4117647058823529, 5.725717590856133, 1.5354635846428564, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(106664, 'HP:0001407', 'Hepatic cysts', 'XPO:0130806', 'increased size of the biliary tree', 0.4153846153846154, 8.69832224767236, 1.900828567057226, 'UPHENO:0087100', 'abnormal hepatobiliary system morphology'),
(106665, 'HP:0001407', 'Hepatic cysts', 'XPO:0141833', 'edematous alimentary system', 0.42857142857142855, 5.725717590856133, 1.5664861849086864, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(106666, 'HP:0001407', 'Hepatic cysts', 'XPO:0140114', 'abnormally necrotic liver and biliary system', 0.41509433962264153, 8.69832224767236, 1.9001642900608593, 'UPHENO:0087100', 'abnormal hepatobiliary system morphology'),
(106667, 'HP:0001407', 'Hepatic cysts', 'XPO:0102522', 'abnormal pharyngeal cavity morphology', 0.44680851063829785, 5.725717590856133, 1.5994684583029237, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(106668, 'HP:0001407', 'Hepatic cysts', 'XPO:0130724', 'increased size of the liver parenchyme', 0.49295774647887325, 10.01729298920255, 2.2221841007837098, 'UPHENO:0019492', 'abnormal liver morphology'),
(106669, 'HP:0001407', 'Hepatic cysts', 'XPO:0129215', 'decreased size of the bile duct', 0.40298507462686567, 8.69832224767236, 1.872243050489645, 'UPHENO:0087100', 'abnormal hepatobiliary system morphology'),
(106670, 'HP:0001407', 'Hepatic cysts', 'XPO:0141125', 'abnormally necrotic liver parenchyme', 0.5072463768115942, 10.01729298920255, 2.2541596159618282, 'UPHENO:0019492', 'abnormal liver morphology'),
(106671, 'HP:0001407', 'Hepatic cysts', 'XPO:0140645', 'abnormally necrotic hepatic vein', 0.4117647058823529, 10.01729298920255, 2.0309524124007297, 'UPHENO:0019492', 'abnormal liver morphology'),
(106672, 'HP:0001407', 'Hepatic cysts', 'XPO:0102825', 'abnormal bile duct morphology', 0.4576271186440678, 8.69832224767236, 1.9951411346668921, 'UPHENO:0087100', 'abnormal hepatobiliary system morphology'),
(106673, 'HP:0001407', 'Hepatic cysts', 'XPO:0130151', 'increased size of the liver', 0.4166666666666667, 10.01729298920255, 2.0430056482629695, 'UPHENO:0019492', 'abnormal liver morphology'),
(106674, 'HP:0001407', 'Hepatic cysts', 'XPO:0130756', 'increased size of the hepatocyte', 0.4074074074074074, 9.184143847054914, 1.9343443938413178, 'UPHENO:0086622', 'abnormal liver morphology'),
(106675, 'HP:0001407', 'Hepatic cysts', 'XPO:0102733', 'abnormal posterior foregut morphology', 0.40384615384615385, 5.725717590856133, 1.520627839767678, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(106676, 'HP:0001407', 'Hepatic cysts', 'XPO:0101784', 'abnormal alimentary system morphology', 0.44680851063829785, 5.725717590856133, 1.5994684583029237, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(106677, 'HP:0001407', 'Hepatic cysts', 'XPO:0102426', 'abnormal liver morphology', 0.546875, 10.01729298920255, 2.3405570070968458, 'UPHENO:0019492', 'abnormal liver morphology'),
(106678, 'HP:0001407', 'Hepatic cysts', 'XPO:0101674', 'abnormal hepatic vein morphology', 0.44871794871794873, 10.01729298920255, 2.1201271569935747, 'UPHENO:0019492', 'abnormal liver morphology'),
(106679, 'HP:0001407', 'Hepatic cysts', 'XPO:0101836', 'abnormal islets of Langerhans morphology', 0.40625, 7.428233084304616, 1.7371585104701155, 'UPHENO:0076812', 'abnormal endocrine system morphology'),
(106680, 'HP:0001407', 'Hepatic cysts', 'XPO:0140388', 'abnormally necrotic biliary tree', 0.42857142857142855, 8.69832224767236, 1.93076471685692, 'UPHENO:0087100', 'abnormal hepatobiliary system morphology'),
(106681, 'HP:0001407', 'Hepatic cysts', 'XPO:0102118', 'abnormal oral evagination morphology', 0.42, 5.725717590856133, 1.5507422055775666, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(106682, 'HP:0001407', 'Hepatic cysts', 'XPO:0100042', 'abnormal hepatic vein', 0.5737704918032787, 10.01729298920255, 2.3974209319500575, 'UPHENO:0019492', 'abnormal liver morphology'),
(106683, 'HP:0001407', 'Hepatic cysts', 'XPO:0102125', 'abnormal liver and biliary system morphology', 0.4583333333333333, 8.69832224767236, 1.9966800019490265, 'UPHENO:0087100', 'abnormal hepatobiliary system morphology'),
(106684, 'HP:0001407', 'Hepatic cysts', 'XPO:0142061', 'abnormal digestive tract morphology', 0.42857142857142855, 5.725717590856133, 1.5664861849086864, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(106685, 'HP:0001407', 'Hepatic cysts', 'XPO:0130596', 'increased size of the hepatic vein', 0.40229885057471265, 10.01729298920255, 2.0074724046487695, 'UPHENO:0019492', 'abnormal liver morphology'),
(106686, 'HP:0001407', 'Hepatic cysts', 'XPO:0102155', 'abnormal midgut morphology', 0.4117647058823529, 5.725717590856133, 1.5354635846428564, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(106687, 'HP:0001407', 'Hepatic cysts', 'XPO:0102801', 'abnormal hepato-pancreatic duct morphology', 0.41509433962264153, 8.69832224767236, 1.9001642900608593, 'UPHENO:0087100', 'abnormal hepatobiliary system morphology'),
(106688, 'HP:0001407', 'Hepatic cysts', 'XPO:0115392', 'abnormally incomplete structure of alimentary system', 0.4375, 5.725717590856133, 1.582719635943005, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(106689, 'HP:0001407', 'Hepatic cysts', 'XPO:0139906', 'abnormally necrotic alimentary system', 0.40384615384615385, 5.725717590856133, 1.520627839767678, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(106690, 'HP:0001407', 'Hepatic cysts', 'XPO:0127068', 'abnormally localised hepatic vein', 0.49295774647887325, 10.01729298920255, 2.2221841007837098, 'UPHENO:0019492', 'abnormal liver morphology'),
(106691, 'HP:0001407', 'Hepatic cysts', 'XPO:0130691', 'increased size of the bile duct', 0.40298507462686567, 8.69832224767236, 1.872243050489645, 'UPHENO:0087100', 'abnormal hepatobiliary system morphology'),
(106692, 'HP:0001407', 'Hepatic cysts', 'XPO:0103168', 'abnormal liver parenchyme morphology', 0.546875, 10.01729298920255, 2.3405570070968458, 'UPHENO:0019492', 'abnormal liver morphology'),
(106693, 'HP:0001407', 'Hepatic cysts', 'XPO:0101857', 'abnormal endocrine system morphology', 0.40425531914893614, 7.428233084304616, 1.7328885527373792, 'UPHENO:0076812', 'abnormal endocrine system morphology'),
(106694, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0140421', 'abnormally necrotic anterior entopeduncular region', 0.46774193548387094, 8.02346099791745, 1.9372426736073256, 'HP:0002060', 'Abnormal cerebral morphology'),
(106695, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0129924', 'increased size of the telencephalon', 0.43283582089552236, 8.02346099791745, 1.8635560972122107, 'HP:0002060', 'Abnormal cerebral morphology'),
(106696, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0142058', 'abnormal cerebrospinal fluid morphology', 0.4772727272727273, 5.483278994082134, 1.617720470261422, 'HP:0002011', 'Morphological central nervous system abnormality'),
(106697, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0128739', 'decreased size of the dorsal telencephalon', 0.4264705882352941, 8.02346099791745, 1.8498027277157947, 'HP:0002060', 'Abnormal cerebral morphology'),
(106698, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0130649', 'increased size of the accessory olfactory bulb', 0.40540540540540543, 8.651717009412357, 1.872819489874467, 'UPHENO:0087531', 'abnormal cerebral hemisphere morphology'),
(106699, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0102274', 'abnormal gustatory system morphology', 0.40425531914893614, 4.7814666189787065, 1.3902997209433732, 'HP:0012639', 'Abnormal nervous system morphology'),
(106700, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0101652', 'abnormal external plexiform layer of the olfactory bulb morphology', 0.4411764705882353, 8.651717009412357, 1.9536975136240373, 'UPHENO:0087531', 'abnormal cerebral hemisphere morphology'),
(106701, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0141044', 'abnormally necrotic anterior amygdala', 0.4027777777777778, 8.02346099791745, 1.7976851200440698, 'HP:0002060', 'Abnormal cerebral morphology'),
(106702, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0140186', 'abnormally necrotic pallium', 0.4393939393939394, 8.02346099791745, 1.8776208710622537, 'HP:0002060', 'Abnormal cerebral morphology'),
(106703, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0101117', 'abnormal tuberal region', 0.4576271186440678, 6.667568321314008, 1.7467856420423753, 'HP:0100547', 'Abnormal forebrain morphology'),
(106704, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0101123', 'abnormal third ventricle', 0.4576271186440678, 6.667568321314008, 1.7467856420423753, 'HP:0100547', 'Abnormal forebrain morphology'),
(106705, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0100988', 'abnormal habenula', 0.4576271186440678, 6.667568321314008, 1.7467856420423753, 'HP:0100547', 'Abnormal forebrain morphology'),
(106706, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0101420', 'abnormal magnocellular preoptic nucleus', 0.43548387096774194, 6.667568321314008, 1.704000722566664, 'HP:0100547', 'Abnormal forebrain morphology'),
(106707, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0101797', 'abnormal lateral pallium morphology', 0.46774193548387094, 8.02346099791745, 1.9372426736073256, 'HP:0002060', 'Abnormal cerebral morphology'),
(106708, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0100195', 'abnormal retromammillary area', 0.46551724137931033, 6.667568321314008, 1.7617797852303152, 'HP:0100547', 'Abnormal forebrain morphology'),
(106709, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0100951', 'abnormal adenohypophysis', 0.45, 6.667568321314008, 1.7321679319833003, 'HP:0100547', 'Abnormal forebrain morphology'),
(106710, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0102696', 'abnormal accessory olfactory bulb morphology', 0.44776119402985076, 8.651717009412357, 1.968223345696023, 'UPHENO:0087531', 'abnormal cerebral hemisphere morphology'),
(106711, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0103200', 'abnormal prosomere 5 morphology', 0.4461538461538462, 8.02346099791745, 1.8920089808682852, 'HP:0002060', 'Abnormal cerebral morphology'),
(106712, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0127764', 'abnormally localised optic chiasm', 0.4153846153846154, 6.667568321314008, 1.6642131181731699, 'HP:0100547', 'Abnormal forebrain morphology'),
(106713, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0102978', 'abnormal prosomere 6 morphology', 0.4461538461538462, 8.02346099791745, 1.8920089808682852, 'HP:0002060', 'Abnormal cerebral morphology'),
(106714, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0101284', 'abnormal ventromedial thalamic nucleus', 0.45, 6.667568321314008, 1.7321679319833003, 'HP:0100547', 'Abnormal forebrain morphology'),
(106715, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0129399', 'decreased size of the medial pallium', 0.42028985507246375, 8.02346099791745, 1.8363494384224073, 'HP:0002060', 'Abnormal cerebral morphology'),
(106716, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0102219', 'abnormal vestibuloauditory system morphology', 0.41304347826086957, 4.7814666189787065, 1.405330425021534, 'HP:0012639', 'Abnormal nervous system morphology'),
(106717, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0102584', 'abnormal dorsal septum morphology', 0.4393939393939394, 8.02346099791745, 1.8776208710622537, 'HP:0002060', 'Abnormal cerebral morphology'),
(106718, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0103075', 'abnormal subthalamic nucleus morphology', 0.4027777777777778, 8.02346099791745, 1.7976851200440698, 'HP:0002060', 'Abnormal cerebral morphology'),
(106719, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0100656', 'abnormal ventral hypothalamic nucleus', 0.45, 6.667568321314008, 1.7321679319833003, 'HP:0100547', 'Abnormal forebrain morphology'),
(106720, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0101825', 'abnormal granule cell layer of the olfactory bulb morphology', 0.4411764705882353, 8.651717009412357, 1.9536975136240373, 'UPHENO:0087531', 'abnormal cerebral hemisphere morphology'),
(106721, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0129429', 'decreased size of the anterior commissure', 0.42028985507246375, 8.02346099791745, 1.8363494384224073, 'HP:0002060', 'Abnormal cerebral morphology'),
(106722, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0140412', 'abnormally necrotic lateral septum', 0.4027777777777778, 8.02346099791745, 1.7976851200440698, 'HP:0002060', 'Abnormal cerebral morphology'),
(106723, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0101354', 'abnormal eminentia thalami', 0.47368421052631576, 6.667568321314008, 1.7771668003909757, 'HP:0100547', 'Abnormal forebrain morphology'),
(106724, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0130846', 'increased size of the anterior entopeduncular region', 0.453125, 8.02346099791745, 1.9067330082319718, 'HP:0002060', 'Abnormal cerebral morphology'),
(106725, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0128766', 'decreased size of the dorsal pallium', 0.42028985507246375, 8.02346099791745, 1.8363494384224073, 'HP:0002060', 'Abnormal cerebral morphology'),
(106726, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0142031', 'abnormally necrotic cerebrospinal fluid', 0.44680851063829785, 5.483278994082134, 1.5652398285119449, 'HP:0002011', 'Morphological central nervous system abnormality'),
(106727, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0102548', 'abnormal principal cavity morphology', 0.41304347826086957, 4.7814666189787065, 1.405330425021534, 'HP:0012639', 'Abnormal nervous system morphology'),
(106728, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0140029', 'abnormally necrotic basal forebrain', 0.4393939393939394, 8.02346099791745, 1.8776208710622537, 'HP:0002060', 'Abnormal cerebral morphology'),
(106729, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0102986', 'abnormal eminentia thalami morphology', 0.421875, 6.667568321314008, 1.677164388351466, 'HP:0100547', 'Abnormal forebrain morphology'),
(106730, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0102968', 'abnormal medial ganglionic eminence morphology', 0.4603174603174603, 8.02346099791745, 1.9218062310018553, 'HP:0002060', 'Abnormal cerebral morphology'),
(106731, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0102007', 'abnormal anterior entopeduncular region morphology', 0.4915254237288136, 8.02346099791745, 1.9858839509832855, 'HP:0002060', 'Abnormal cerebral morphology'),
(106732, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0141224', 'abnormally necrotic dorsal telencephalon', 0.4393939393939394, 8.02346099791745, 1.8776208710622537, 'HP:0002060', 'Abnormal cerebral morphology'),
(106733, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0141179', 'abnormally necrotic bed nucleus of the stria terminalis', 0.410958904109589, 8.651717009412357, 1.8856033890652597, 'UPHENO:0087531', 'abnormal cerebral hemisphere morphology'),
(106734, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0126877', 'abnormally localised diencephalon', 0.421875, 6.667568321314008, 1.677164388351466, 'HP:0100547', 'Abnormal forebrain morphology'),
(106735, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0128708', 'decreased size of the basal forebrain', 0.4264705882352941, 8.02346099791745, 1.8498027277157947, 'HP:0002060', 'Abnormal cerebral morphology'),
(106736, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0130873', 'increased size of the medial pallium', 0.42028985507246375, 8.02346099791745, 1.8363494384224073, 'HP:0002060', 'Abnormal cerebral morphology'),
(106737, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0100946', 'abnormal melanotrope', 0.42857142857142855, 6.667568321314008, 1.6904228111816126, 'HP:0100547', 'Abnormal forebrain morphology'),
(106738, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0101184', 'abnormal suprachiasmatic nucleus', 0.4426229508196721, 6.667568321314008, 1.7179111633526845, 'HP:0100547', 'Abnormal forebrain morphology'),
(106739, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0140476', 'abnormally necrotic lateral ganglionic eminence', 0.4264705882352941, 8.02346099791745, 1.8498027277157947, 'HP:0002060', 'Abnormal cerebral morphology'),
(106740, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0141233', 'abnormally necrotic lateral amygdala', 0.4027777777777778, 8.02346099791745, 1.7976851200440698, 'HP:0002060', 'Abnormal cerebral morphology'),
(106741, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0100971', 'abnormal prethalamus basal plate', 0.45, 6.667568321314008, 1.7321679319833003, 'HP:0100547', 'Abnormal forebrain morphology'),
(106742, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0101351', 'abnormal dorsal habenular nucleus', 0.43548387096774194, 6.667568321314008, 1.704000722566664, 'HP:0100547', 'Abnormal forebrain morphology'),
(106743, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0101838', 'abnormal nucleus accumbens morphology', 0.43283582089552236, 8.02346099791745, 1.8635560972122107, 'HP:0002060', 'Abnormal cerebral morphology'),
(106744, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0102238', 'abnormal basal forebrain morphology', 0.47540983606557374, 8.02346099791745, 1.9530571619126922, 'HP:0002060', 'Abnormal cerebral morphology'),
(106745, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0103128', 'abnormal subcommissural organ morphology', 0.4090909090909091, 6.667568321314008, 1.6515573214369805, 'HP:0100547', 'Abnormal forebrain morphology'),
(106746, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0101293', 'abnormal posterior hypothalamus', 0.46551724137931033, 6.667568321314008, 1.7617797852303152, 'HP:0100547', 'Abnormal forebrain morphology'),
(106747, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0101671', 'abnormal olfactory bulb morphology', 0.4411764705882353, 8.651717009412357, 1.9536975136240373, 'UPHENO:0087531', 'abnormal cerebral hemisphere morphology'),
(106748, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0127531', 'abnormally localised pretectum', 0.4153846153846154, 6.667568321314008, 1.6642131181731699, 'HP:0100547', 'Abnormal forebrain morphology'),
(106749, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0128482', 'decreased size of the ventral pallium', 0.42028985507246375, 8.02346099791745, 1.8363494384224073, 'HP:0002060', 'Abnormal cerebral morphology'),
(106750, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0101663', 'abnormal central nervous system morphology', 0.4666666666666667, 5.483278994082134, 1.5996448138795258, 'HP:0002011', 'Morphological central nervous system abnormality'),
(106751, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0100783', 'abnormal supraoptoparaventricular region', 0.4426229508196721, 6.667568321314008, 1.7179111633526845, 'HP:0100547', 'Abnormal forebrain morphology'),
(106752, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0103133', 'abnormal parabrachial area morphology', 0.4375, 5.483278994082134, 1.5488494310006167, 'HP:0002011', 'Morphological central nervous system abnormality'),
(106753, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0100698', 'abnormal optic stalk', 0.4576271186440678, 6.667568321314008, 1.7467856420423753, 'HP:0100547', 'Abnormal forebrain morphology'),
(106754, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0140020', 'abnormally necrotic amygdala', 0.4264705882352941, 8.02346099791745, 1.8498027277157947, 'HP:0002060', 'Abnormal cerebral morphology'),
(106755, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0107380', 'abnormal dorsal telencephalon morphology', 0.47540983606557374, 8.02346099791745, 1.9530571619126922, 'HP:0002060', 'Abnormal cerebral morphology'),
(106756, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0101789', 'abnormal optic tract morphology', 0.40298507462686567, 6.667568321314008, 1.639185931352649, 'HP:0100547', 'Abnormal forebrain morphology'),
(106757, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0100491', 'abnormal pars distalis', 0.4426229508196721, 6.667568321314008, 1.7179111633526845, 'HP:0100547', 'Abnormal forebrain morphology'),
(106758, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0139876', 'abnormally necrotic mitral cell layer of the olfactory bulb', 0.410958904109589, 8.651717009412357, 1.8856033890652597, 'UPHENO:0087531', 'abnormal cerebral hemisphere morphology'),
(106759, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0129962', 'increased size of the ventral pallium', 0.42028985507246375, 8.02346099791745, 1.8363494384224073, 'HP:0002060', 'Abnormal cerebral morphology'),
(106760, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0140838', 'abnormally necrotic anterior commissure', 0.43283582089552236, 8.02346099791745, 1.8635560972122107, 'HP:0002060', 'Abnormal cerebral morphology'),
(106761, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0102191', 'abnormal telencephalon morphology', 0.48333333333333334, 8.02346099791745, 1.969265383079039, 'HP:0002060', 'Abnormal cerebral morphology'),
(106762, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0142037', 'decreased size of the cerebrospinal fluid', 0.42857142857142855, 5.483278994082134, 1.5329633758669794, 'HP:0002011', 'Morphological central nervous system abnormality'),
(106763, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0101866', 'abnormal anterior entopeduncular nucleus morphology', 0.43283582089552236, 8.02346099791745, 1.8635560972122107, 'HP:0002060', 'Abnormal cerebral morphology'),
(106764, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0130557', 'increased size of the medial ganglionic eminence', 0.4142857142857143, 8.02346099791745, 1.8231854734408677, 'HP:0002060', 'Abnormal cerebral morphology'),
(106765, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0127266', 'abnormally localised anterior hypothalamus', 0.4090909090909091, 6.667568321314008, 1.6515573214369805, 'HP:0100547', 'Abnormal forebrain morphology'),
(106766, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0139879', 'abnormally necrotic telencephalon', 0.4461538461538462, 8.02346099791745, 1.8920089808682852, 'HP:0002060', 'Abnormal cerebral morphology'),
(106767, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0101970', 'abnormal lateral ganglionic eminence morphology', 0.4603174603174603, 8.02346099791745, 1.9218062310018553, 'HP:0002060', 'Abnormal cerebral morphology'),
(106768, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0102755', 'abnormal third ventricle morphology', 0.4153846153846154, 6.667568321314008, 1.6642131181731699, 'HP:0100547', 'Abnormal forebrain morphology'),
(106769, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0141259', 'abnormally necrotic accessory olfactory bulb', 0.4166666666666667, 8.651717009412357, 1.8986527031701055, 'UPHENO:0087531', 'abnormal cerebral hemisphere morphology'),
(106770, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0102395', 'abnormal pretectum morphology', 0.4153846153846154, 6.667568321314008, 1.6642131181731699, 'HP:0100547', 'Abnormal forebrain morphology'),
(106771, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0129908', 'increased size of the ventral pallidum', 0.4027777777777778, 8.02346099791745, 1.7976851200440698, 'HP:0002060', 'Abnormal cerebral morphology'),
(106772, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0126700', 'abnormally localised infundibulum', 0.40298507462686567, 6.667568321314008, 1.639185931352649, 'HP:0100547', 'Abnormal forebrain morphology'),
(106773, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0127516', 'abnormally localised eminentia thalami', 0.4153846153846154, 6.667568321314008, 1.6642131181731699, 'HP:0100547', 'Abnormal forebrain morphology'),
(106774, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0130244', 'increased size of the dorsal pallium', 0.42028985507246375, 8.02346099791745, 1.8363494384224073, 'HP:0002060', 'Abnormal cerebral morphology'),
(106775, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0128187', 'decreased size of the basal ganglion', 0.4142857142857143, 8.02346099791745, 1.8231854734408677, 'HP:0002060', 'Abnormal cerebral morphology'),
(106776, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0102760', 'abnormal dorsal pallidum morphology', 0.4461538461538462, 8.02346099791745, 1.8920089808682852, 'HP:0002060', 'Abnormal cerebral morphology'),
(106777, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0140076', 'abnormally necrotic granule cell layer of the olfactory bulb', 0.410958904109589, 8.651717009412357, 1.8856033890652597, 'UPHENO:0087531', 'abnormal cerebral hemisphere morphology'),
(106778, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0128240', 'decreased size of the pallidum', 0.4084507042253521, 8.02346099791745, 1.810300608993995, 'HP:0002060', 'Abnormal cerebral morphology'),
(106779, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0129196', 'decreased size of the dorsal pallidum', 0.4027777777777778, 8.02346099791745, 1.7976851200440698, 'HP:0002060', 'Abnormal cerebral morphology'),
(106780, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0126930', 'abnormally localised subcommissural organ', 0.4090909090909091, 6.667568321314008, 1.6515573214369805, 'HP:0100547', 'Abnormal forebrain morphology'),
(106781, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0102249', 'abnormal forebrain morphology', 0.4576271186440678, 6.667568321314008, 1.7467856420423753, 'HP:0100547', 'Abnormal forebrain morphology'),
(106782, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0100157', 'abnormal optic tract', 0.47368421052631576, 6.667568321314008, 1.7771668003909757, 'HP:0100547', 'Abnormal forebrain morphology'),
(106783, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0102633', 'abnormal ventricular zone morphology', 0.42105263157894735, 6.005340694266148, 1.590146063369307, 'UPHENO:0081435', 'abnormal anatomical entity morphology in the brain'),
(106784, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0141255', 'abnormally necrotic prosomere 5', 0.4027777777777778, 8.02346099791745, 1.7976851200440698, 'HP:0002060', 'Abnormal cerebral morphology'),
(106785, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0102357', 'abnormal subpallium morphology', 0.47540983606557374, 8.02346099791745, 1.9530571619126922, 'HP:0002060', 'Abnormal cerebral morphology'),
(106786, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0102174', 'abnormal pallium morphology', 0.47540983606557374, 8.02346099791745, 1.9530571619126922, 'HP:0002060', 'Abnormal cerebral morphology'),
(106787, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0131746', 'abnormal neural tube closure', 0.4375, 5.483278994082134, 1.5488494310006167, 'HP:0002011', 'Morphological central nervous system abnormality'),
(106788, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0129757', 'increased size of the striatum', 0.4084507042253521, 8.02346099791745, 1.810300608993995, 'HP:0002060', 'Abnormal cerebral morphology'),
(106789, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0103057', 'abnormal medial amygdala morphology', 0.4393939393939394, 8.02346099791745, 1.8776208710622537, 'HP:0002060', 'Abnormal cerebral morphology'),
(106790, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0100194', 'abnormal preoptic area', 0.4576271186440678, 6.667568321314008, 1.7467856420423753, 'HP:0100547', 'Abnormal forebrain morphology'),
(106791, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0139993', 'abnormally necrotic pallidum', 0.42028985507246375, 8.02346099791745, 1.8363494384224073, 'HP:0002060', 'Abnormal cerebral morphology'),
(106792, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0140228', 'abnormally necrotic telencephalon septum', 0.4084507042253521, 8.02346099791745, 1.810300608993995, 'HP:0002060', 'Abnormal cerebral morphology'),
(106793, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0139760', 'abnormally necrotic basal ganglion', 0.4264705882352941, 8.02346099791745, 1.8498027277157947, 'HP:0002060', 'Abnormal cerebral morphology'),
(106794, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0101268', 'abnormal lateral hypothalamic nucleus', 0.45, 6.667568321314008, 1.7321679319833003, 'HP:0100547', 'Abnormal forebrain morphology'),
(106795, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0139757', 'abnormally necrotic neural nucleus', 0.4117647058823529, 5.483278994082134, 1.502604659339613, 'HP:0002011', 'Morphological central nervous system abnormality'),
(106796, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0102685', 'abnormal anterior hypothalamus morphology', 0.40298507462686567, 6.667568321314008, 1.639185931352649, 'HP:0100547', 'Abnormal forebrain morphology'),
(106797, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0139852', 'abnormally necrotic neuromere', 0.40384615384615385, 5.483278994082134, 1.4880863994491305, 'HP:0002011', 'Morphological central nervous system abnormality'),
(106798, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0100962', 'abnormal dorsal thalamus', 0.46551724137931033, 6.667568321314008, 1.7617797852303152, 'HP:0100547', 'Abnormal forebrain morphology'),
(106799, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0101905', 'abnormal visual system morphology', 0.41304347826086957, 4.7814666189787065, 1.405330425021534, 'HP:0012639', 'Abnormal nervous system morphology'),
(106800, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0126924', 'abnormally localised preoptic area', 0.40298507462686567, 6.667568321314008, 1.639185931352649, 'HP:0100547', 'Abnormal forebrain morphology'),
(106801, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0129173', 'decreased size of the accessory olfactory bulb', 0.40540540540540543, 8.651717009412357, 1.872819489874467, 'UPHENO:0087531', 'abnormal cerebral hemisphere morphology'),
(106802, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0128277', 'decreased size of the striatum', 0.4084507042253521, 8.02346099791745, 1.810300608993995, 'HP:0002060', 'Abnormal cerebral morphology'),
(106803, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0126519', 'abnormally localised habenula', 0.40298507462686567, 6.667568321314008, 1.639185931352649, 'HP:0100547', 'Abnormal forebrain morphology'),
(106804, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0126581', 'abnormally localised prethalamus', 0.4090909090909091, 6.667568321314008, 1.6515573214369805, 'HP:0100547', 'Abnormal forebrain morphology'),
(106805, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0140065', 'abnormally necrotic ventral pallidum', 0.4142857142857143, 8.02346099791745, 1.8231854734408677, 'HP:0002060', 'Abnormal cerebral morphology'),
(106806, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0126384', 'abnormally localised posterior hypothalamus', 0.4090909090909091, 6.667568321314008, 1.6515573214369805, 'HP:0100547', 'Abnormal forebrain morphology'),
(106807, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0127253', 'abnormally localised zona limitans intrathalamica', 0.40298507462686567, 6.667568321314008, 1.639185931352649, 'HP:0100547', 'Abnormal forebrain morphology'),
(106808, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0103040', 'abnormal nucleus of the diagonal band morphology', 0.4461538461538462, 8.02346099791745, 1.8920089808682852, 'HP:0002060', 'Abnormal cerebral morphology'),
(106809, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0102604', 'abnormal ventral pallidum morphology', 0.4461538461538462, 8.02346099791745, 1.8920089808682852, 'HP:0002060', 'Abnormal cerebral morphology'),
(106810, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0102951', 'abnormal lateral amygdala morphology', 0.4393939393939394, 8.02346099791745, 1.8776208710622537, 'HP:0002060', 'Abnormal cerebral morphology'),
(106811, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0101795', 'abnormal central amygdala morphology', 0.4155844155844156, 9.4405603741242, 1.980744750307267, 'UPHENO:0081603', 'abnormal cerebral cortex morphology'),
(106812, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0100998', 'abnormal rostral tuberal region', 0.45, 6.667568321314008, 1.7321679319833003, 'HP:0100547', 'Abnormal forebrain morphology'),
(106813, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0130183', 'increased size of the lateral pallium', 0.42028985507246375, 8.02346099791745, 1.8363494384224073, 'HP:0002060', 'Abnormal cerebral morphology'),
(106814, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0141149', 'abnormally necrotic dorsal pallium', 0.43283582089552236, 8.02346099791745, 1.8635560972122107, 'HP:0002060', 'Abnormal cerebral morphology'),
(106815, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0102327', 'abnormal zona limitans intrathalamica morphology', 0.4090909090909091, 6.667568321314008, 1.6515573214369805, 'HP:0100547', 'Abnormal forebrain morphology'),
(106816, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0102066', 'abnormal ventral pallium morphology', 0.46774193548387094, 8.02346099791745, 1.9372426736073256, 'HP:0002060', 'Abnormal cerebral morphology'),
(106817, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0128428', 'decreased size of the ventral pallidum', 0.4027777777777778, 8.02346099791745, 1.7976851200440698, 'HP:0002060', 'Abnormal cerebral morphology'),
(106818, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0101106', 'abnormal caudal tuberal region', 0.45, 6.667568321314008, 1.7321679319833003, 'HP:0100547', 'Abnormal forebrain morphology'),
(106819, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0142044', 'increased size of the cerebrospinal fluid', 0.42857142857142855, 5.483278994082134, 1.5329633758669794, 'HP:0002011', 'Morphological central nervous system abnormality'),
(106820, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0140544', 'abnormally necrotic forebrain', 0.421875, 6.667568321314008, 1.677164388351466, 'HP:0100547', 'Abnormal forebrain morphology'),
(106821, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0127076', 'abnormally localised dorsal thalamus', 0.4090909090909091, 6.667568321314008, 1.6515573214369805, 'HP:0100547', 'Abnormal forebrain morphology'),
(106822, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0103107', 'abnormal ventral septum morphology', 0.4393939393939394, 8.02346099791745, 1.8776208710622537, 'HP:0002060', 'Abnormal cerebral morphology'),
(106823, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0101068', 'abnormal pineal gland', 0.42857142857142855, 6.667568321314008, 1.6904228111816126, 'HP:0100547', 'Abnormal forebrain morphology'),
(106824, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0130082', 'increased size of the subpallium', 0.4264705882352941, 8.02346099791745, 1.8498027277157947, 'HP:0002060', 'Abnormal cerebral morphology'),
(106825, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0130903', 'increased size of the anterior commissure', 0.42028985507246375, 8.02346099791745, 1.8363494384224073, 'HP:0002060', 'Abnormal cerebral morphology'),
(106826, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0140574', 'abnormally necrotic medial ganglionic eminence', 0.4264705882352941, 8.02346099791745, 1.8498027277157947, 'HP:0002060', 'Abnormal cerebral morphology'),
(106827, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0102603', 'abnormal prethalamus basal plate morphology', 0.40298507462686567, 6.667568321314008, 1.639185931352649, 'HP:0100547', 'Abnormal forebrain morphology'),
(106828, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0141028', 'abnormally necrotic external plexiform layer of the olfactory bulb', 0.410958904109589, 8.651717009412357, 1.8856033890652597, 'UPHENO:0087531', 'abnormal cerebral hemisphere morphology'),
(106829, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0102854', 'abnormal medial septum morphology', 0.4393939393939394, 8.02346099791745, 1.8776208710622537, 'HP:0002060', 'Abnormal cerebral morphology'),
(106830, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0101496', 'abnormal subcommissural organ', 0.46551724137931033, 6.667568321314008, 1.7617797852303152, 'HP:0100547', 'Abnormal forebrain morphology'),
(106831, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0100909', 'abnormal choroid fissure', 0.42857142857142855, 6.667568321314008, 1.6904228111816126, 'HP:0100547', 'Abnormal forebrain morphology'),
(106832, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0101526', 'abnormal infundibulum', 0.4576271186440678, 6.667568321314008, 1.7467856420423753, 'HP:0100547', 'Abnormal forebrain morphology'),
(106833, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0128602', 'decreased size of the subpallium', 0.4264705882352941, 8.02346099791745, 1.8498027277157947, 'HP:0002060', 'Abnormal cerebral morphology'),
(106834, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0101906', 'abnormal sensory system morphology', 0.4318181818181818, 4.7814666189787065, 1.4369148276191301, 'HP:0012639', 'Abnormal nervous system morphology'),
(106835, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0140424', 'abnormally necrotic dorsal septum', 0.4027777777777778, 8.02346099791745, 1.7976851200440698, 'HP:0002060', 'Abnormal cerebral morphology'),
(106836, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0130217', 'increased size of the dorsal telencephalon', 0.4264705882352941, 8.02346099791745, 1.8498027277157947, 'HP:0002060', 'Abnormal cerebral morphology'),
(106837, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0101443', 'abnormal subthalamic nucleus', 0.421875, 6.667568321314008, 1.677164388351466, 'HP:0100547', 'Abnormal forebrain morphology'),
(106838, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0103102', 'abnormal anterior amygdala morphology', 0.4393939393939394, 8.02346099791745, 1.8776208710622537, 'HP:0002060', 'Abnormal cerebral morphology'),
(106839, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0126680', 'abnormally localised tuberal region', 0.40298507462686567, 6.667568321314008, 1.639185931352649, 'HP:0100547', 'Abnormal forebrain morphology'),
(106840, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0140129', 'abnormally necrotic nucleus of the diagonal band', 0.4084507042253521, 8.02346099791745, 1.810300608993995, 'HP:0002060', 'Abnormal cerebral morphology'),
(106841, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0101987', 'abnormal striatum morphology', 0.453125, 8.02346099791745, 1.9067330082319718, 'HP:0002060', 'Abnormal cerebral morphology'),
(106842, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0100729', 'abnormal thalamus', 0.47368421052631576, 6.667568321314008, 1.7771668003909757, 'HP:0100547', 'Abnormal forebrain morphology'),
(106843, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0115310', 'abnormally incomplete structure of forebrain', 0.45, 6.667568321314008, 1.7321679319833003, 'HP:0100547', 'Abnormal forebrain morphology'),
(106844, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0128704', 'decreased size of the lateral pallium', 0.42028985507246375, 8.02346099791745, 1.8363494384224073, 'HP:0002060', 'Abnormal cerebral morphology'),
(106845, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0101851', 'abnormal basal ganglion morphology', 0.4603174603174603, 8.02346099791745, 1.9218062310018553, 'HP:0002060', 'Abnormal cerebral morphology'),
(106846, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0129127', 'decreased size of the lateral ganglionic eminence', 0.4142857142857143, 8.02346099791745, 1.8231854734408677, 'HP:0002060', 'Abnormal cerebral morphology'),
(106847, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0128276', 'decreased size of the amygdala', 0.4142857142857143, 8.02346099791745, 1.8231854734408677, 'HP:0002060', 'Abnormal cerebral morphology'),
(106848, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0107340', 'abnormal enteric nervous system morphology', 0.4222222222222222, 4.7814666189787065, 1.4208594094232423, 'HP:0012639', 'Abnormal nervous system morphology'),
(106849, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0102490', 'abnormal presumptive midbrain-hindbrain boundary morphology', 0.42857142857142855, 5.483278994082134, 1.5329633758669794, 'HP:0002011', 'Morphological central nervous system abnormality'),
(106850, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0101664', 'abnormal nervous system morphology', 0.4418604651162791, 4.7814666189787065, 1.4535271116150168, 'HP:0012639', 'Abnormal nervous system morphology'),
(106851, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0101053', 'abnormal anterior hypothalamus', 0.46551724137931033, 6.667568321314008, 1.7617797852303152, 'HP:0100547', 'Abnormal forebrain morphology'),
(106852, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0100233', 'abnormal pars nervosa', 0.4426229508196721, 6.667568321314008, 1.7179111633526845, 'HP:0100547', 'Abnormal forebrain morphology'),
(106853, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0102200', 'abnormal telencephalon septum morphology', 0.4461538461538462, 8.02346099791745, 1.8920089808682852, 'HP:0002060', 'Abnormal cerebral morphology'),
(106854, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0140910', 'abnormally necrotic ventral septum', 0.4027777777777778, 8.02346099791745, 1.7976851200440698, 'HP:0002060', 'Abnormal cerebral morphology'),
(106855, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0129720', 'increased size of the pallidum', 0.4084507042253521, 8.02346099791745, 1.810300608993995, 'HP:0002060', 'Abnormal cerebral morphology'),
(106856, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0101186', 'abnormal optic chiasm', 0.47368421052631576, 6.667568321314008, 1.7771668003909757, 'HP:0100547', 'Abnormal forebrain morphology'),
(106857, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0101986', 'abnormal amygdala morphology', 0.4603174603174603, 8.02346099791745, 1.9218062310018553, 'HP:0002060', 'Abnormal cerebral morphology'),
(106858, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0140854', 'abnormally necrotic ventral pallium', 0.43283582089552236, 8.02346099791745, 1.8635560972122107, 'HP:0002060', 'Abnormal cerebral morphology'),
(106859, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0129372', 'decreased size of the anterior entopeduncular region', 0.453125, 8.02346099791745, 1.9067330082319718, 'HP:0002060', 'Abnormal cerebral morphology'),
(106860, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0100914', 'abnormal pars intermedia', 0.4426229508196721, 6.667568321314008, 1.7179111633526845, 'HP:0100547', 'Abnormal forebrain morphology'),
(106861, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0127949', 'abnormally localised optic tract', 0.4153846153846154, 6.667568321314008, 1.6642131181731699, 'HP:0100547', 'Abnormal forebrain morphology'),
(106862, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0101790', 'abnormal neuromere morphology', 0.44680851063829785, 5.483278994082134, 1.5652398285119449, 'HP:0002011', 'Morphological central nervous system abnormality'),
(106863, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0128444', 'decreased size of the telencephalon', 0.43283582089552236, 8.02346099791745, 1.8635560972122107, 'HP:0002060', 'Abnormal cerebral morphology'),
(106864, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0102282', 'abnormal prosomere morphology', 0.4032258064516129, 6.65028457999709, 1.637548888705938, 'UPHENO:0087518', 'abnormal forebrain morphology'),
(106865, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0140575', 'abnormally necrotic medial septum', 0.4027777777777778, 8.02346099791745, 1.7976851200440698, 'HP:0002060', 'Abnormal cerebral morphology'),
(106866, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0140330', 'abnormally necrotic dorsal pallidum', 0.4142857142857143, 8.02346099791745, 1.8231854734408677, 'HP:0002060', 'Abnormal cerebral morphology'),
(106867, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0127530', 'abnormally localised third ventricle', 0.4090909090909091, 6.667568321314008, 1.6515573214369805, 'HP:0100547', 'Abnormal forebrain morphology'),
(106868, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0102620', 'abnormal habenula morphology', 0.4090909090909091, 6.667568321314008, 1.6515573214369805, 'HP:0100547', 'Abnormal forebrain morphology'),
(106869, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0100695', 'abnormal zona limitans intrathalamica', 0.46551724137931033, 6.667568321314008, 1.7617797852303152, 'HP:0100547', 'Abnormal forebrain morphology'),
(106870, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0100263', 'abnormal prethalamus', 0.46551724137931033, 6.667568321314008, 1.7617797852303152, 'HP:0100547', 'Abnormal forebrain morphology'),
(106871, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0102361', 'abnormal thalamus morphology', 0.421875, 6.667568321314008, 1.677164388351466, 'HP:0100547', 'Abnormal forebrain morphology'),
(106872, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0129080', 'decreased size of the medial ganglionic eminence', 0.4142857142857143, 8.02346099791745, 1.8231854734408677, 'HP:0002060', 'Abnormal cerebral morphology'),
(106873, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0100575', 'abnormal diencephalon', 0.48214285714285715, 6.667568321314008, 1.7929641492884176, 'HP:0100547', 'Abnormal forebrain morphology'),
(106874, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0101862', 'abnormal brain ventricle morphology', 0.41379310344827586, 6.005340694266148, 1.5763783058468588, 'UPHENO:0081435', 'abnormal anatomical entity morphology in the brain'),
(106875, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0102826', 'abnormal anterior commissure morphology', 0.46774193548387094, 8.02346099791745, 1.9372426736073256, 'HP:0002060', 'Abnormal cerebral morphology'),
(106876, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0130672', 'increased size of the dorsal pallidum', 0.4027777777777778, 8.02346099791745, 1.7976851200440698, 'HP:0002060', 'Abnormal cerebral morphology'),
(106877, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0100315', 'abnormal neurohypophysis', 0.45, 6.667568321314008, 1.7321679319833003, 'HP:0100547', 'Abnormal forebrain morphology'),
(106878, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0100473', 'abnormal ventral habenular nucleus', 0.43548387096774194, 6.667568321314008, 1.704000722566664, 'HP:0100547', 'Abnormal forebrain morphology'),
(106879, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0102207', 'abnormal diencephalon morphology', 0.42857142857142855, 6.667568321314008, 1.6904228111816126, 'HP:0100547', 'Abnormal forebrain morphology'),
(106880, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0141227', 'abnormally necrotic medial amygdala', 0.4027777777777778, 8.02346099791745, 1.7976851200440698, 'HP:0002060', 'Abnormal cerebral morphology'),
(106881, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0127125', 'abnormally localised retromammillary area', 0.4090909090909091, 6.667568321314008, 1.6515573214369805, 'HP:0100547', 'Abnormal forebrain morphology'),
(106882, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0102247', 'abnormal mitral cell layer of the olfactory bulb morphology', 0.4411764705882353, 8.651717009412357, 1.9536975136240373, 'UPHENO:0087531', 'abnormal cerebral hemisphere morphology'),
(106883, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0128429', 'decreased size of the pallium', 0.4264705882352941, 8.02346099791745, 1.8498027277157947, 'HP:0002060', 'Abnormal cerebral morphology'),
(106884, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0102389', 'abnormal bed nucleus of the stria terminalis morphology', 0.44776119402985076, 8.651717009412357, 1.968223345696023, 'UPHENO:0087531', 'abnormal cerebral hemisphere morphology'),
(106885, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0130187', 'increased size of the basal forebrain', 0.4264705882352941, 8.02346099791745, 1.8498027277157947, 'HP:0002060', 'Abnormal cerebral morphology'),
(106886, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0102594', 'abnormal dorsal thalamus morphology', 0.4153846153846154, 6.667568321314008, 1.6642131181731699, 'HP:0100547', 'Abnormal forebrain morphology'),
(106887, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0103178', 'abnormal dorsal pallium morphology', 0.46774193548387094, 8.02346099791745, 1.9372426736073256, 'HP:0002060', 'Abnormal cerebral morphology'),
(106888, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0140226', 'abnormally necrotic subpallium', 0.4393939393939394, 8.02346099791745, 1.8776208710622537, 'HP:0002060', 'Abnormal cerebral morphology'),
(106889, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0127938', 'abnormally localised mammilary region', 0.40298507462686567, 6.667568321314008, 1.639185931352649, 'HP:0100547', 'Abnormal forebrain morphology'),
(106890, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0140628', 'abnormally necrotic glomerular layer of the olfactory bulb', 0.410958904109589, 8.651717009412357, 1.8856033890652597, 'UPHENO:0087531', 'abnormal cerebral hemisphere morphology'),
(106891, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0140571', 'abnormally necrotic medial pallium', 0.43283582089552236, 8.02346099791745, 1.8635560972122107, 'HP:0002060', 'Abnormal cerebral morphology'),
(106892, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0102169', 'abnormal medium cavity morphology', 0.41304347826086957, 4.7814666189787065, 1.405330425021534, 'HP:0012639', 'Abnormal nervous system morphology'),
(106893, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0101140', 'abnormal ventrolateral thalamic nucleus', 0.45, 6.667568321314008, 1.7321679319833003, 'HP:0100547', 'Abnormal forebrain morphology'),
(106894, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0102442', 'abnormal medial pallium morphology', 0.46774193548387094, 8.02346099791745, 1.9372426736073256, 'HP:0002060', 'Abnormal cerebral morphology'),
(106895, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0102131', 'abnormal glomerular layer of the olfactory bulb morphology', 0.4411764705882353, 8.651717009412357, 1.9536975136240373, 'UPHENO:0087531', 'abnormal cerebral hemisphere morphology'),
(106896, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0140066', 'abnormally necrotic prosomere 6', 0.4027777777777778, 8.02346099791745, 1.7976851200440698, 'HP:0002060', 'Abnormal cerebral morphology'),
(106897, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0100611', 'abnormal hypophysis', 0.4576271186440678, 6.667568321314008, 1.7467856420423753, 'HP:0100547', 'Abnormal forebrain morphology'),
(106898, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0101564', 'abnormal anterior thalamic nucleus', 0.45, 6.667568321314008, 1.7321679319833003, 'HP:0100547', 'Abnormal forebrain morphology'),
(106899, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0101895', 'abnormal prethalamus morphology', 0.4153846153846154, 6.667568321314008, 1.6642131181731699, 'HP:0100547', 'Abnormal forebrain morphology'),
(106900, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0101588', 'abnormal central nucleus of the thalamus', 0.45, 6.667568321314008, 1.7321679319833003, 'HP:0100547', 'Abnormal forebrain morphology'),
(106901, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0140468', 'abnormally necrotic central nervous system', 0.4117647058823529, 5.483278994082134, 1.502604659339613, 'HP:0002011', 'Morphological central nervous system abnormality'),
(106902, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0140045', 'abnormally necrotic lateral pallium', 0.43283582089552236, 8.02346099791745, 1.8635560972122107, 'HP:0002060', 'Abnormal cerebral morphology'),
(106903, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0139738', 'abnormally necrotic olfactory bulb', 0.410958904109589, 8.651717009412357, 1.8856033890652597, 'UPHENO:0087531', 'abnormal cerebral hemisphere morphology'),
(106904, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0101075', 'abnormal mammilary region', 0.4576271186440678, 6.667568321314008, 1.7467856420423753, 'HP:0100547', 'Abnormal forebrain morphology'),
(106905, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0101595', 'abnormal prosomere 4', 0.4576271186440678, 6.667568321314008, 1.7467856420423753, 'HP:0100547', 'Abnormal forebrain morphology'),
(106906, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0101805', 'abnormal pallidum morphology', 0.453125, 8.02346099791745, 1.9067330082319718, 'HP:0002060', 'Abnormal cerebral morphology'),
(106907, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0100763', 'abnormal pretectum', 0.47368421052631576, 6.667568321314008, 1.7771668003909757, 'HP:0100547', 'Abnormal forebrain morphology'),
(106908, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0102509', 'abnormal lateral septum morphology', 0.4393939393939394, 8.02346099791745, 1.8776208710622537, 'HP:0002060', 'Abnormal cerebral morphology'),
(106909, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0101827', 'abnormal retromammillary area morphology', 0.40298507462686567, 6.667568321314008, 1.639185931352649, 'HP:0100547', 'Abnormal forebrain morphology'),
(106910, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0129667', 'increased size of the basal ganglion', 0.4142857142857143, 8.02346099791745, 1.8231854734408677, 'HP:0002060', 'Abnormal cerebral morphology'),
(106911, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0102972', 'abnormal lateral forebrain bundle morphology', 0.4098360655737705, 6.65028457999709, 1.6509168565412138, 'UPHENO:0087518', 'abnormal forebrain morphology'),
(106912, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0130603', 'increased size of the lateral ganglionic eminence', 0.4142857142857143, 8.02346099791745, 1.8231854734408677, 'HP:0002060', 'Abnormal cerebral morphology'),
(106913, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0102059', 'abnormal olfactory system morphology', 0.40425531914893614, 4.7814666189787065, 1.3902997209433732, 'HP:0012639', 'Abnormal nervous system morphology'),
(106914, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0101796', 'abnormal neural nucleus morphology', 0.45652173913043476, 5.483278994082134, 1.5821618319614958, 'HP:0002011', 'Morphological central nervous system abnormality'),
(106915, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0129909', 'increased size of the pallium', 0.4264705882352941, 8.02346099791745, 1.8498027277157947, 'HP:0002060', 'Abnormal cerebral morphology'),
(106916, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0140021', 'abnormally necrotic striatum', 0.42028985507246375, 8.02346099791745, 1.8363494384224073, 'HP:0002060', 'Abnormal cerebral morphology'),
(106917, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0102925', 'abnormal posterior hypothalamus morphology', 0.40298507462686567, 6.667568321314008, 1.639185931352649, 'HP:0100547', 'Abnormal forebrain morphology'),
(106918, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0127143', 'abnormally localised thalamus', 0.4153846153846154, 6.667568321314008, 1.6642131181731699, 'HP:0100547', 'Abnormal forebrain morphology'),
(106919, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0100590', 'abnormal hypothalamus', 0.47368421052631576, 6.667568321314008, 1.7771668003909757, 'HP:0100547', 'Abnormal forebrain morphology'),
(106920, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0127340', 'abnormally localised hypothalamus', 0.4153846153846154, 6.667568321314008, 1.6642131181731699, 'HP:0100547', 'Abnormal forebrain morphology'),
(106921, 'HP:0025714', 'Cerebral cortical microinfarct', 'XPO:0129756', 'increased size of the amygdala', 0.4142857142857143, 8.02346099791745, 1.8231854734408677, 'HP:0002060', 'Abnormal cerebral morphology'),
(106922, 'HP:0012432', 'Chronic fatigue', 'XPO:0100004', 'abnormal cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(106923, 'HP:0012432', 'Chronic fatigue', 'XPO:0107271', 'abnormal apical region', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(106924, 'HP:0012432', 'Chronic fatigue', 'XPO:0131685', 'abnormal cortical actin cytoskeleton', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(106925, 'HP:0012432', 'Chronic fatigue', 'XPO:0100392', 'abnormal cilium', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(106926, 'HP:0012432', 'Chronic fatigue', 'XPO:0100638', 'abnormal polar body', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(106927, 'HP:0012432', 'Chronic fatigue', 'XPO:0100176', 'abnormal stage VI oocyte', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(106928, 'HP:0012432', 'Chronic fatigue', 'XPO:0131694', 'abnormal RNA polymerase II activity', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(106929, 'HP:0012432', 'Chronic fatigue', 'XPO:0131666', 'abnormal adherens junction', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(106930, 'HP:0012432', 'Chronic fatigue', 'XPO:0100533', 'abnormal melanoblast', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(106931, 'HP:0012432', 'Chronic fatigue', 'XPO:0115508', 'abnormally peramorphic growth of whole organism', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(106932, 'HP:0012432', 'Chronic fatigue', 'XPO:0100422', 'abnormal notochord', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(106933, 'HP:0012432', 'Chronic fatigue', 'XPO:0141265', 'abnormal escape behavior', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(106934, 'HP:0012432', 'Chronic fatigue', 'XPO:0131725', 'abnormal phosphorylation of RNA polymerase II C-terminal domain', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(106935, 'HP:0012432', 'Chronic fatigue', 'XPO:0141964', 'absent cilium motility in olfactory pit', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(106936, 'HP:0012432', 'Chronic fatigue', 'XPO:0131722', 'abnormal determination of left/right symmetry', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(106937, 'HP:0012432', 'Chronic fatigue', 'XPO:0100989', 'abnormal right blastomere', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(106938, 'HP:0012432', 'Chronic fatigue', 'XPO:0133388', 'absent insulin receptor signaling pathway', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(106939, 'HP:0012432', 'Chronic fatigue', 'XPO:0100014', 'abnormal tissue', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(106940, 'HP:0012432', 'Chronic fatigue', 'XPO:0107339', 'abnormal yolk platelet', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(106941, 'HP:0012432', 'Chronic fatigue', 'XPO:0141797', 'abnormal hydrogen metabolic process', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(106942, 'HP:0012432', 'Chronic fatigue', 'XPO:0100665', 'abnormal egg jelly', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(106943, 'HP:0012432', 'Chronic fatigue', 'XPO:0107261', 'abnormal dorsal-ventral axis', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(106944, 'HP:0012432', 'Chronic fatigue', 'XPO:0100642', 'abnormal gustatory system', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(106945, 'HP:0012432', 'Chronic fatigue', 'XPO:0100308', 'abnormal early embryonic cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(106946, 'HP:0012432', 'Chronic fatigue', 'XPO:0101221', 'abnormal larval immune system', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(106947, 'HP:0012432', 'Chronic fatigue', 'XPO:0100574', 'abnormal gastrula cell', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(106948, 'HP:0012432', 'Chronic fatigue', 'XPO:0100573', 'abnormal extraembryonic structure', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(106949, 'HP:0012432', 'Chronic fatigue', 'XPO:0131469', 'abnormal heart process', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(106950, 'HP:0012432', 'Chronic fatigue', 'XPO:0100032', 'abnormal nervous system', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(106951, 'HP:0012432', 'Chronic fatigue', 'XPO:0100477', 'abnormal pericyte', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(106952, 'HP:0012432', 'Chronic fatigue', 'XPO:0100585', 'abnormal elastica externa', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(106953, 'HP:0012432', 'Chronic fatigue', 'XPO:0100344', 'abnormal portion of organism substance', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(106954, 'HP:0012432', 'Chronic fatigue', 'XPO:0101463', 'abnormal right-ventral blastomere', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(106955, 'HP:0012432', 'Chronic fatigue', 'XPO:0141791', 'abnormal primary metabolic process', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(106956, 'HP:0012432', 'Chronic fatigue', 'XPO:0101435', 'abnormal paracrine cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(106957, 'HP:0012432', 'Chronic fatigue', 'XPO:0101237', 'abnormal mucus secreting cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(106958, 'HP:0012432', 'Chronic fatigue', 'XPO:0141499', 'abnormal tadpole', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(106959, 'HP:0012432', 'Chronic fatigue', 'XPO:0141898', 'abnormal maltose metabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(106960, 'HP:0012432', 'Chronic fatigue', 'XPO:0100626', 'abnormal primordial germ cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(106961, 'HP:0012432', 'Chronic fatigue', 'XPO:0141778', 'abnormal biosynthetic process', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(106962, 'HP:0012432', 'Chronic fatigue', 'XPO:0141271', 'increased surface breathing', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(106963, 'HP:0012432', 'Chronic fatigue', 'XPO:0107272', 'abnormal axial region', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(106964, 'HP:0012432', 'Chronic fatigue', 'XPO:0100501', 'abnormal urogenital system', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(106965, 'HP:0012432', 'Chronic fatigue', 'XPO:0100062', 'abnormal anatomical space', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(106966, 'HP:0012432', 'Chronic fatigue', 'XPO:0100423', 'abnormal process', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(106967, 'HP:0012432', 'Chronic fatigue', 'XPO:0100823', 'abnormal blood', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(106968, 'HP:0012432', 'Chronic fatigue', 'XPO:00000000', 'Xenopus phenotype', 0.5714285714285714, 1.4755025719078136, 0.918228907628411, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(106969, 'HP:0012432', 'Chronic fatigue', 'XPO:0100274', 'abnormal sensory system', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(106970, 'HP:0012432', 'Chronic fatigue', 'XPO:0107263', 'abnormal anatomical side', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(106971, 'HP:0012432', 'Chronic fatigue', 'XPO:0100003', 'abnormal organism subdivision', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(106972, 'HP:0012432', 'Chronic fatigue', 'XPO:0101461', 'abnormal sperm entry point', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(106973, 'HP:0012432', 'Chronic fatigue', 'XPO:0100218', 'abnormal epithelial cell', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(106974, 'HP:0012432', 'Chronic fatigue', 'XPO:0100084', 'abnormal anatomical group', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(106975, 'HP:0012432', 'Chronic fatigue', 'XPO:0141771', 'abnormal urea homeostasis', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(106976, 'HP:0012432', 'Chronic fatigue', 'XPO:0101228', 'abnormal mesenchymal stem cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(106977, 'HP:0012432', 'Chronic fatigue', 'XPO:0101570', 'abnormal forelimb region', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(106978, 'HP:0012432', 'Chronic fatigue', 'XPO:0115512', 'abnormally semi-erect whole organism', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(106979, 'HP:0012432', 'Chronic fatigue', 'XPO:0100842', 'abnormal left-dorsal blastomere', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(106980, 'HP:0012432', 'Chronic fatigue', 'XPO:0101141', 'abnormal Keller explant', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(106981, 'HP:0012432', 'Chronic fatigue', 'XPO:0107262', 'abnormal left-right axis', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(106982, 'HP:0012432', 'Chronic fatigue', 'XPO:0100427', 'abnormal olfactory system', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(106983, 'HP:0012432', 'Chronic fatigue', 'XPO:0100515', 'abnormal somatic stem cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(106984, 'HP:0012432', 'Chronic fatigue', 'XPO:0101448', 'abnormal myelin accumulating cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(106985, 'HP:0012432', 'Chronic fatigue', 'XPO:0141892', 'abnormal inositol metabolic process', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(106986, 'HP:0012432', 'Chronic fatigue', 'XPO:0107258', 'abnormal anatomical axis', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(106987, 'HP:0012432', 'Chronic fatigue', 'XPO:0107273', 'abnormal basal region', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(106988, 'HP:0012432', 'Chronic fatigue', 'XPO:0116434', 'abnormal biological process', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(106989, 'HP:0012432', 'Chronic fatigue', 'XPO:0131667', 'abnormal actin cytoskeleton', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(106990, 'HP:0012432', 'Chronic fatigue', 'XPO:0100599', 'abnormal adult immune system', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(106991, 'HP:0012432', 'Chronic fatigue', 'XPO:0141267', 'abnormal resting posture', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(106992, 'HP:0012432', 'Chronic fatigue', 'XPO:0101110', 'abnormal cell-free extract', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(106993, 'HP:0012432', 'Chronic fatigue', 'XPO:0141738', 'abnormal carbon dioxide homeostasis', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(106994, 'HP:0012432', 'Chronic fatigue', 'XPO:0100108', 'abnormal cell part', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(106995, 'HP:0012432', 'Chronic fatigue', 'XPO:0141958', 'absent cilium motility in left-right organizer', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(106996, 'HP:0012432', 'Chronic fatigue', 'XPO:0141960', 'absent cilium motility in brain', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(106997, 'HP:0012432', 'Chronic fatigue', 'XPO:0101241', 'abnormal nucleate erythrocyte', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(106998, 'HP:0012432', 'Chronic fatigue', 'XPO:0100721', 'abnormal centromere', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(106999, 'HP:0012432', 'Chronic fatigue', 'XPO:0107278', 'abnormal medial region', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(107000, 'HP:0012432', 'Chronic fatigue', 'XPO:0101480', 'abnormal stage V oocyte', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(107001, 'HP:0012432', 'Chronic fatigue', 'XPO:0107284', 'abnormal migrating myoblast', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(107002, 'HP:0012432', 'Chronic fatigue', 'XPO:0141276', 'decreased surface breathing', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(107003, 'HP:0012432', 'Chronic fatigue', 'XPO:0101569', 'abnormal activin-induced ectoderm', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(107004, 'HP:0012432', 'Chronic fatigue', 'XPO:0133340', 'abnormal cell adhesion', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(107005, 'HP:0012432', 'Chronic fatigue', 'XPO:0141783', 'abnormal collagen metabolic process', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(107006, 'HP:0012432', 'Chronic fatigue', 'XPO:0131723', 'abnormal pathway-restricted SMAD protein phosphorylation', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(107007, 'HP:0012432', 'Chronic fatigue', 'XPO:0141911', 'abnormal ribose phosphate metabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(107008, 'HP:0012432', 'Chronic fatigue', 'XPO:0101347', 'abnormal hindlimb region', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(107009, 'HP:0012432', 'Chronic fatigue', 'XPO:0128000', 'absent behavior', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(107010, 'HP:0012432', 'Chronic fatigue', 'XPO:0141745', 'abnormal creatinine homeostasis', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(107011, 'HP:0012432', 'Chronic fatigue', 'XPO:0141600', 'absent metamorphosis', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(107012, 'HP:0012432', 'Chronic fatigue', 'XPO:0100899', 'abnormal secondary spermatogonium', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(107013, 'HP:0012432', 'Chronic fatigue', 'XPO:0101311', 'abnormal bottle cell', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(107014, 'HP:0012432', 'Chronic fatigue', 'XPO:0107253', 'abnormal enteric nervous system', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(107015, 'HP:0012432', 'Chronic fatigue', 'XPO:0141792', 'abnormal small molecule metabolic process', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(107016, 'HP:0012432', 'Chronic fatigue', 'XPO:0101071', 'abnormal endoplasmic reticulum', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(107017, 'HP:0012432', 'Chronic fatigue', 'XPO:0133403', 'abnormal developmental process', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(107018, 'HP:0012432', 'Chronic fatigue', 'XPO:0131745', 'abnormal axis elongation', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(107019, 'HP:0012432', 'Chronic fatigue', 'XPO:0101061', 'abnormal plasma membrane', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(107020, 'HP:0012432', 'Chronic fatigue', 'XPO:0101157', 'abnormal female organism', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(107021, 'HP:0012432', 'Chronic fatigue', 'XPO:0100902', 'abnormal spermatocyte', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(107022, 'HP:0012432', 'Chronic fatigue', 'XPO:0141266', 'abnormal surface breathing', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(107023, 'HP:0012432', 'Chronic fatigue', 'XPO:0131744', 'abnormal apical constriction', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(107024, 'HP:0012432', 'Chronic fatigue', 'XPO:0100481', 'abnormal anatomical line', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(107025, 'HP:0012432', 'Chronic fatigue', 'XPO:0101072', 'abnormal mitochondrial cloud', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(107026, 'HP:0012432', 'Chronic fatigue', 'XPO:0100653', 'abnormal myoblast', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(107027, 'HP:0012432', 'Chronic fatigue', 'XPO:0100028', 'abnormal anatomical cluster', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(107028, 'HP:0012432', 'Chronic fatigue', 'XPO:0100372', 'abnormal hematological system', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(107029, 'HP:0012432', 'Chronic fatigue', 'XPO:0100715', 'abnormal ciliated cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(107030, 'HP:0012432', 'Chronic fatigue', 'XPO:0100317', 'abnormal respiratory system', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(107031, 'HP:0012432', 'Chronic fatigue', 'XPO:0131740', 'abnormal detection of nodal flow', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(107032, 'HP:0012432', 'Chronic fatigue', 'XPO:0107260', 'abnormal anterior-posterior axis', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(107033, 'HP:0012432', 'Chronic fatigue', 'XPO:0141754', 'abnormal homeostatic process', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(107034, 'HP:0012432', 'Chronic fatigue', 'XPO:0101109', 'abnormal egg cell-free extract', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(107035, 'HP:0012432', 'Chronic fatigue', 'XPO:0100546', 'abnormal whole organism', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(107036, 'HP:0012432', 'Chronic fatigue', 'XPO:0101302', 'abnormal subcortical cytoplasm', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(107037, 'HP:0012432', 'Chronic fatigue', 'XPO:0101535', 'abnormal absorptive cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(107038, 'HP:0012432', 'Chronic fatigue', 'XPO:0100549', 'abnormal mitotic cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(107039, 'HP:0012432', 'Chronic fatigue', 'XPO:0100784', 'abnormal left blastomere', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(107040, 'HP:0012432', 'Chronic fatigue', 'XPO:0141962', 'absent cilium motility in pronephric kidney', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(107041, 'HP:0012432', 'Chronic fatigue', 'XPO:0107276', 'abnormal dorsal region', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(107042, 'HP:0012432', 'Chronic fatigue', 'XPO:0101498', 'abnormal stage II oocyte', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(107043, 'HP:0012432', 'Chronic fatigue', 'XPO:0131730', 'abnormal regulation of protein folding', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(107044, 'HP:0012432', 'Chronic fatigue', 'XPO:0141782', 'abnormal methylation', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(107045, 'HP:0012432', 'Chronic fatigue', 'XPO:0100969', 'abnormal disaggregated/reaggregated ectoderm treated with activin', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(107046, 'HP:0012432', 'Chronic fatigue', 'XPO:0100417', 'abnormal dense regular connective tissue', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(107047, 'HP:0012432', 'Chronic fatigue', 'XPO:0141264', 'abnormal schooling behavior', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(107048, 'HP:0012432', 'Chronic fatigue', 'XPO:0141770', 'abnormal urate homeostasis', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(107049, 'HP:0012432', 'Chronic fatigue', 'XPO:0115505', 'dead whole organism', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(107050, 'HP:0012432', 'Chronic fatigue', 'XPO:0100009', 'abnormal multi-tissue structure', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(107051, 'HP:0012432', 'Chronic fatigue', 'XPO:0100205', 'abnormal limb segment', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(107052, 'HP:0012432', 'Chronic fatigue', 'XPO:0100104', 'abnormal embryonic structure', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(107053, 'HP:0012432', 'Chronic fatigue', 'XPO:0116494', 'absent biological process', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(107054, 'HP:0012432', 'Chronic fatigue', 'XPO:0141787', 'abnormal hormone metabolic process', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(107055, 'HP:0012432', 'Chronic fatigue', 'XPO:0141263', 'abnormal visually guided collision avoidance behavior', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(107056, 'HP:0012432', 'Chronic fatigue', 'XPO:0107259', 'abnormal animal-vegetal axis', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(107057, 'HP:0012432', 'Chronic fatigue', 'XPO:0100031', 'abnormal central nervous system', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(107058, 'HP:0012432', 'Chronic fatigue', 'XPO:0100152', 'abnormal alimentary system', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(107059, 'HP:0012432', 'Chronic fatigue', 'XPO:0101240', 'abnormal ciliated non-epidermal cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(107060, 'HP:0012432', 'Chronic fatigue', 'XPO:0101220', 'abnormal centriole', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(107061, 'HP:0012432', 'Chronic fatigue', 'XPO:0100172', 'abnormal stem cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(107062, 'HP:0012432', 'Chronic fatigue', 'XPO:0100688', 'abnormal adipose tissue', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(107063, 'HP:0012432', 'Chronic fatigue', 'XPO:0100289', 'abnormal chondroblast', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(107064, 'HP:0012432', 'Chronic fatigue', 'XPO:0141959', 'absent cilium motility in floor plate', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(107065, 'HP:0012432', 'Chronic fatigue', 'XPO:0101513', 'abnormal basal body', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(107066, 'HP:0012432', 'Chronic fatigue', 'XPO:0100674', 'abnormal secondary oogonium', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(107067, 'HP:0012432', 'Chronic fatigue', 'XPO:0116433', 'abnormal axis specification', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(107068, 'HP:0012432', 'Chronic fatigue', 'XPO:0100888', 'abnormal microtubule', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(107069, 'HP:0012432', 'Chronic fatigue', 'XPO:0100862', 'abnormal blastomere V1', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(107070, 'HP:0012432', 'Chronic fatigue', 'XPO:0100307', 'abnormal blastomere', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(107071, 'HP:0012432', 'Chronic fatigue', 'XPO:0101405', 'abnormal ring structure', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(107072, 'HP:0012432', 'Chronic fatigue', 'XPO:0101467', 'abnormal alkali secreting cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(107073, 'HP:0012432', 'Chronic fatigue', 'XPO:0141860', 'abnormal malate-aspartate shuttle', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(107074, 'HP:0012432', 'Chronic fatigue', 'XPO:0141794', 'abnormal prosthetic group metabolic process', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(107075, 'HP:0012432', 'Chronic fatigue', 'XPO:0141724', 'abnormal prevention of polyspermy', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(107076, 'HP:0012432', 'Chronic fatigue', 'XPO:0100551', 'abnormal oocyte cortex', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(107077, 'HP:0012432', 'Chronic fatigue', 'XPO:0101451', 'abnormal dorsal lymph space', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(107078, 'HP:0012432', 'Chronic fatigue', 'XPO:0100754', 'abnormal electrically active cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(107079, 'HP:0012432', 'Chronic fatigue', 'XPO:0100025', 'abnormal oocyte', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(107080, 'HP:0012432', 'Chronic fatigue', 'XPO:0141796', 'abnormal demethylation', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(107081, 'HP:0012432', 'Chronic fatigue', 'XPO:0141784', 'abnormal cellular hormone metabolic process', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(107082, 'HP:0012432', 'Chronic fatigue', 'XPO:0131691', 'abnormal molecular function', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(107083, 'HP:0012432', 'Chronic fatigue', 'XPO:0101004', 'abnormal acid secreting cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(107084, 'HP:0012432', 'Chronic fatigue', 'XPO:0100437', 'abnormal proepicardium', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(107085, 'HP:0012432', 'Chronic fatigue', 'XPO:0100081', 'abnormal anatomical entity in vitro', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(107086, 'HP:0012432', 'Chronic fatigue', 'XPO:0141315', 'abnormal anatomical region', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(107087, 'HP:0012432', 'Chronic fatigue', 'XPO:0100337', 'abnormal zygote', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(107088, 'HP:0012432', 'Chronic fatigue', 'XPO:0101264', 'abnormal mitotic spindle', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(107089, 'HP:0012432', 'Chronic fatigue', 'XPO:0101497', 'abnormal ciliary axoneme', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(107090, 'HP:0012432', 'Chronic fatigue', 'XPO:0101113', 'abnormal stage IV oocyte', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(107091, 'HP:0012432', 'Chronic fatigue', 'XPO:0141743', 'abnormal chemical homeostasis within a tissue', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(107092, 'HP:0012432', 'Chronic fatigue', 'XPO:0141781', 'abnormal secondary metabolic process', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(107093, 'HP:0012432', 'Chronic fatigue', 'XPO:0101409', 'abnormal perivitelline space', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(107094, 'HP:0012432', 'Chronic fatigue', 'XPO:0141786', 'abnormal pigment metabolic process', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(107095, 'HP:0012432', 'Chronic fatigue', 'XPO:0141904', 'abnormal glucosamine metabolic process', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(107096, 'HP:0012432', 'Chronic fatigue', 'XPO:0100503', 'abnormal blastomere D2', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(107097, 'HP:0012432', 'Chronic fatigue', 'XPO:0100545', 'abnormal male organism', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(107098, 'HP:0012432', 'Chronic fatigue', 'XPO:0107312', 'abnormal filopodium', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(107099, 'HP:0012432', 'Chronic fatigue', 'XPO:0100277', 'abnormal blastocoel', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(107100, 'HP:0012432', 'Chronic fatigue', 'XPO:0100465', 'abnormal skeletal system', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(107101, 'HP:0012432', 'Chronic fatigue', 'XPO:0100239', 'abnormal acellular anatomical structure', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(107102, 'HP:0012432', 'Chronic fatigue', 'XPO:0100762', 'abnormal intersomitic region', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(107103, 'HP:0012432', 'Chronic fatigue', 'XPO:0100202', 'abnormal embryo', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(107104, 'HP:0012432', 'Chronic fatigue', 'XPO:0141795', 'abnormal glycosylation', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(107105, 'HP:0012432', 'Chronic fatigue', 'XPO:0101547', 'abnormal lampbrush chromosome', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(107106, 'HP:0012432', 'Chronic fatigue', 'XPO:0141809', 'abnormal catalytic activity', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(107107, 'HP:0012432', 'Chronic fatigue', 'XPO:0131675', 'abnormal spindle microtubule', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(107108, 'HP:0012432', 'Chronic fatigue', 'XPO:0101297', 'abnormal barrier cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(107109, 'HP:0012432', 'Chronic fatigue', 'XPO:0100295', 'abnormal extracellular matrix', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(107110, 'HP:0012432', 'Chronic fatigue', 'XPO:0100429', 'abnormal spermatid', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(107111, 'HP:0012432', 'Chronic fatigue', 'XPO:0101136', 'abnormal ooplasm', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(107112, 'HP:0012432', 'Chronic fatigue', 'XPO:0131729', 'abnormal regulation of growth rate', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(107113, 'HP:0012432', 'Chronic fatigue', 'XPO:0100285', 'abnormal progenitor cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(107114, 'HP:0012432', 'Chronic fatigue', 'XPO:0101132', 'abnormal apoptotic cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(107115, 'HP:0012432', 'Chronic fatigue', 'XPO:0100273', 'abnormal visual system', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(107116, 'HP:0012432', 'Chronic fatigue', 'XPO:0131677', 'abnormal actin filament', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(107117, 'HP:0012432', 'Chronic fatigue', 'XPO:0100907', 'abnormal cytoplasm', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(107118, 'HP:0012432', 'Chronic fatigue', 'XPO:0100852', 'abnormal interdigital region', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(107119, 'HP:0012432', 'Chronic fatigue', 'XPO:0141777', 'abnormal catabolic process', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(107120, 'HP:0012432', 'Chronic fatigue', 'XPO:0100006', 'abnormal anatomical structure', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(107121, 'HP:0012432', 'Chronic fatigue', 'XPO:0100643', 'abnormal thoracic region', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(107122, 'HP:0012432', 'Chronic fatigue', 'XPO:0141907', 'abnormal putrescine metabolic process', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(107123, 'HP:0012432', 'Chronic fatigue', 'XPO:0100976', 'abnormal multiciliated cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(107124, 'HP:0012432', 'Chronic fatigue', 'XPO:0100894', 'abnormal nucleus', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(107125, 'HP:0012432', 'Chronic fatigue', 'XPO:0100026', 'abnormal germ cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(107126, 'HP:0012432', 'Chronic fatigue', 'XPO:0100691', 'abnormal keratin accumulating cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(107127, 'HP:0012432', 'Chronic fatigue', 'XPO:0100956', 'abnormal centrosome', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(107128, 'HP:0012432', 'Chronic fatigue', 'XPO:0101472', 'abnormal zygote cortex', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(107129, 'HP:0012432', 'Chronic fatigue', 'XPO:0101389', 'abnormal wedge region', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(107130, 'HP:0012432', 'Chronic fatigue', 'XPO:0100225', 'abnormal endocrine system', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(107131, 'HP:0012432', 'Chronic fatigue', 'XPO:0101468', 'abnormal stage I oocyte', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(107132, 'HP:0012432', 'Chronic fatigue', 'XPO:0141975', 'abnormal cilium motility', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(107133, 'HP:0012432', 'Chronic fatigue', 'XPO:0141272', 'absent surface breathing', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(107134, 'HP:0012432', 'Chronic fatigue', 'XPO:0141772', 'abnormal water homeostasis', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(107135, 'HP:0012432', 'Chronic fatigue', 'XPO:0100581', 'abnormal immune system', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(107136, 'HP:0012432', 'Chronic fatigue', 'XPO:0101283', 'abnormal left-ventral blastomere', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(107137, 'HP:0012432', 'Chronic fatigue', 'XPO:0101411', 'abnormal marginal zone (sensu neural)', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(107138, 'HP:0012432', 'Chronic fatigue', 'XPO:0133401', 'absent determination of left/right symmetry in lateral plate mesoderm', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(107139, 'HP:0012432', 'Chronic fatigue', 'XPO:0141877', 'abnormal 2-deoxyribose 1-phosphate metabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(107140, 'HP:0012432', 'Chronic fatigue', 'XPO:0100386', 'abnormal limb', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(107141, 'HP:0012432', 'Chronic fatigue', 'XPO:0101575', 'abnormal vitelline membrane', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(107142, 'HP:0012432', 'Chronic fatigue', 'XPO:0101200', 'abnormal joint region', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(107143, 'HP:0012432', 'Chronic fatigue', 'XPO:0116429', 'abnormal behavior', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(107144, 'HP:0012432', 'Chronic fatigue', 'XPO:0131703', 'abnormal cell division', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(107145, 'HP:0012432', 'Chronic fatigue', 'XPO:0100917', 'abnormal stage III oocyte', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(107146, 'HP:0012432', 'Chronic fatigue', 'XPO:0107270', 'abnormal proximal-distal axis', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(107147, 'HP:0012432', 'Chronic fatigue', 'XPO:0141790', 'abnormal cellular metabolic process', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(107148, 'HP:0012432', 'Chronic fatigue', 'XPO:0100070', 'abnormal anatomical system', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(107149, 'HP:0012432', 'Chronic fatigue', 'XPO:0100802', 'abnormal exocrine cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(107150, 'HP:0012432', 'Chronic fatigue', 'XPO:0101378', 'abnormal blastomere D1', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(107151, 'HP:0012432', 'Chronic fatigue', 'XPO:0131719', 'abnormal activation of meiosis', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(107152, 'HP:0012432', 'Chronic fatigue', 'XPO:0101326', 'abnormal cementoblast', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(107153, 'HP:0012432', 'Chronic fatigue', 'XPO:0141798', 'abnormal lipid metabolic process', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(107154, 'HP:0012432', 'Chronic fatigue', 'XPO:0100587', 'abnormal vestibuloauditory system', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(107155, 'HP:0012432', 'Chronic fatigue', 'XPO:0101373', 'abnormal oxygen accumulating cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(107156, 'HP:0012432', 'Chronic fatigue', 'XPO:0131687', 'abnormal astral microtubule', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(107157, 'HP:0012432', 'Chronic fatigue', 'XPO:0100704', 'abnormal Merkel cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(107158, 'HP:0012432', 'Chronic fatigue', 'XPO:0101366', 'abnormal morula cell', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(107159, 'HP:0012432', 'Chronic fatigue', 'XPO:0100258', 'abnormal organ part', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(107160, 'HP:0012432', 'Chronic fatigue', 'XPO:0100232', 'abnormal lymphatic system', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(107161, 'HP:0012432', 'Chronic fatigue', 'XPO:0100887', 'abnormal right-dorsal blastomere', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(107162, 'HP:0012432', 'Chronic fatigue', 'XPO:0100791', 'abnormal multiciliated cell precursor', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(107163, 'HP:0012432', 'Chronic fatigue', 'XPO:0100377', 'abnormal connective tissue', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(107164, 'HP:0012432', 'Chronic fatigue', 'XPO:0142057', 'abnormal desmosome', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(107165, 'HP:0012432', 'Chronic fatigue', 'XPO:0115509', 'abnormally semi-viable whole organism', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(107166, 'HP:0012432', 'Chronic fatigue', 'XPO:0101333', 'abnormal barrier epithelial cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(107167, 'HP:0012432', 'Chronic fatigue', 'XPO:0100724', 'abnormal kinetochore', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(107168, 'HP:0012432', 'Chronic fatigue', 'XPO:0100728', 'abnormal cell condensation', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(107169, 'HP:0012432', 'Chronic fatigue', 'XPO:0141776', 'abnormal metabolic process', 0.5263157894736842, 1.8210412618256888, 0.9790009036675816, 'HP:0000118', 'Phenotypic abnormality'),
(107170, 'HP:0012432', 'Chronic fatigue', 'XPO:0141775', 'abnormal nitrogen compound metabolic process', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(107171, 'HP:0012432', 'Chronic fatigue', 'XPO:0100010', 'abnormal multicellular anatomical structure', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(107172, 'HP:0012432', 'Chronic fatigue', 'XPO:0131669', 'abnormal Roux spot', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(107173, 'HP:0012432', 'Chronic fatigue', 'XPO:0141748', 'abnormal gas homeostasis', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(107174, 'HP:0012432', 'Chronic fatigue', 'XPO:0100547', 'abnormal blastomere V2', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(107175, 'HP:0008237', 'Hypothalamic hypothyroidism', 'XPO:0100233', 'abnormal pars nervosa', 0.41333333333333333, 7.431510076152836, 1.7526239846232008, 'UPHENO:0004618', 'abnormal diencephalon'),
(107176, 'HP:0008237', 'Hypothalamic hypothyroidism', 'XPO:0101068', 'abnormal pineal gland', 0.4025974025974026, 7.431510076152836, 1.7297128819649685, 'UPHENO:0004618', 'abnormal diencephalon'),
(107177, 'HP:0008237', 'Hypothalamic hypothyroidism', 'XPO:0100611', 'abnormal hypophysis', 0.4246575342465753, 7.431510076152836, 1.776470305034014, 'UPHENO:0004618', 'abnormal diencephalon'),
(107178, 'HP:0008237', 'Hypothalamic hypothyroidism', 'XPO:0100946', 'abnormal melanotrope', 0.4025974025974026, 7.431510076152836, 1.7297128819649685, 'UPHENO:0004618', 'abnormal diencephalon'),
(107179, 'HP:0008237', 'Hypothalamic hypothyroidism', 'XPO:0100575', 'abnormal diencephalon', 0.4027777777777778, 7.431510076152836, 1.7301003190584074, 'UPHENO:0004618', 'abnormal diencephalon'),
(107180, 'HP:0008237', 'Hypothalamic hypothyroidism', 'XPO:0100914', 'abnormal pars intermedia', 0.41333333333333333, 7.431510076152836, 1.7526239846232008, 'UPHENO:0004618', 'abnormal diencephalon'),
(107181, 'HP:0008237', 'Hypothalamic hypothyroidism', 'XPO:0100951', 'abnormal adenohypophysis', 0.4189189189189189, 7.431510076152836, 1.7644262996897884, 'UPHENO:0004618', 'abnormal diencephalon'),
(107182, 'HP:0008237', 'Hypothalamic hypothyroidism', 'XPO:0100491', 'abnormal pars distalis', 0.41333333333333333, 7.431510076152836, 1.7526239846232008, 'UPHENO:0004618', 'abnormal diencephalon'),
(107183, 'HP:0008237', 'Hypothalamic hypothyroidism', 'XPO:0100315', 'abnormal neurohypophysis', 0.4189189189189189, 7.431510076152836, 1.7644262996897884, 'UPHENO:0004618', 'abnormal diencephalon'),
(107184, 'HP:0008237', 'Hypothalamic hypothyroidism', 'XPO:0101526', 'abnormal infundibulum', 0.4246575342465753, 7.431510076152836, 1.776470305034014, 'UPHENO:0004618', 'abnormal diencephalon'),
(107185, 'HP:0012461', 'Bacteriuria', 'XPO:0100085', 'abnormal mesonephric sinus', 0.42857142857142855, 6.355235291121788, 1.6503551943819923, 'HP:0000079', 'Abnormality of the urinary system'),
(107186, 'HP:0012461', 'Bacteriuria', 'XPO:0100120', 'abnormal genital system', 0.40625, 5.4478002382576385, 1.4876722914648124, 'HP:0000119', 'Abnormality of the genitourinary system'),
(107187, 'HP:0012461', 'Bacteriuria', 'XPO:0124921', 'absent urinary system', 0.41025641025641024, 6.355235291121788, 1.61470617044417, 'HP:0000079', 'Abnormality of the urinary system'),
(107188, 'HP:0012461', 'Bacteriuria', 'XPO:0100501', 'abnormal urogenital system', 0.4482758620689655, 5.4478002382576385, 1.562727534851952, 'HP:0000119', 'Abnormality of the genitourinary system'),
(107189, 'HP:0012461', 'Bacteriuria', 'XPO:0101579', 'abnormal urethra', 0.40540540540540543, 6.355235291121788, 1.6051313776896794, 'HP:0000079', 'Abnormality of the urinary system'),
(107190, 'HP:0012461', 'Bacteriuria', 'XPO:0101212', 'abnormal glomeral mesenchyme', 0.40625, 5.4478002382576385, 1.4876722914648124, 'HP:0000119', 'Abnormality of the genitourinary system'),
(107191, 'HP:0012461', 'Bacteriuria', 'XPO:0100069', 'abnormal urinary system', 0.5, 6.355235291121788, 1.7825873458433654, 'HP:0000079', 'Abnormality of the urinary system'),
(107192, 'HP:0012461', 'Bacteriuria', 'XPO:0100761', 'abnormal ureter', 0.40540540540540543, 6.355235291121788, 1.6051313776896794, 'HP:0000079', 'Abnormality of the urinary system'),
(107193, 'HP:0012461', 'Bacteriuria', 'XPO:0126535', 'abnormally localised urinary system', 0.42105263157894735, 6.355235291121788, 1.6358143365401303, 'HP:0000079', 'Abnormality of the urinary system'),
(107194, 'HP:0012461', 'Bacteriuria', 'XPO:0101701', 'abnormal urinary system morphology', 0.42105263157894735, 6.355235291121788, 1.6358143365401303, 'HP:0000079', 'Abnormality of the urinary system'),
(107195, 'HP:0007915', 'Polymorphous posterior corneal dystrophy', 'XPO:0102513', 'abnormal sclera morphology', 0.4189189189189189, 6.887869297006056, 1.6986638159319787, 'HP:0012372', 'Abnormal eye morphology'),
(107196, 'HP:0007915', 'Polymorphous posterior corneal dystrophy', 'XPO:0141337', 'increased pigmentation in the eye', 0.40789473684210525, 6.887869297006056, 1.6761639640277146, 'HP:0012372', 'Abnormal eye morphology'),
(107197, 'HP:0007915', 'Polymorphous posterior corneal dystrophy', 'XPO:0100710', 'abnormal hyaloid vein', 0.4626865671641791, 6.887869297006056, 1.7851959556606887, 'HP:0012372', 'Abnormal eye morphology'),
(107198, 'HP:0007915', 'Polymorphous posterior corneal dystrophy', 'XPO:0102862', 'abnormal iris morphology', 0.425, 9.014833150514745, 1.957371729889028, 'UPHENO:0021038', 'abnormal anterior segment of eyeball morphology'),
(107199, 'HP:0007915', 'Polymorphous posterior corneal dystrophy', 'XPO:0128807', 'decreased size of the lens transitional zone', 0.40963855421686746, 9.014833150514745, 1.9216719850908865, 'UPHENO:0021038', 'abnormal anterior segment of eyeball morphology'),
(107200, 'HP:0007915', 'Polymorphous posterior corneal dystrophy', 'XPO:0133372', 'eye fused with olfactory epithelium', 0.40789473684210525, 6.887869297006056, 1.6761639640277146, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(107201, 'HP:0007915', 'Polymorphous posterior corneal dystrophy', 'XPO:0129947', 'increased size of the lens', 0.4146341463414634, 9.014833150514745, 1.9333539892565992, 'UPHENO:0021038', 'abnormal anterior segment of eyeball morphology'),
(107202, 'HP:0007915', 'Polymorphous posterior corneal dystrophy', 'XPO:0133369', 'eye fused with brain', 0.40789473684210525, 6.887869297006056, 1.6761639640277146, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(107203, 'HP:0007915', 'Polymorphous posterior corneal dystrophy', 'XPO:0140375', 'abnormally necrotic lens', 0.43037974683544306, 9.014833150514745, 1.969721200851099, 'UPHENO:0021038', 'abnormal anterior segment of eyeball morphology'),
(107204, 'HP:0007915', 'Polymorphous posterior corneal dystrophy', 'XPO:0103048', 'abnormal cornea morphology', 0.5135135135135135, 10.582693223545188, 2.331170517070414, 'UPHENO:0020998', 'abnormal cornea morphology'),
(107205, 'HP:0007915', 'Polymorphous posterior corneal dystrophy', 'XPO:0100371', 'abnormal hyaloid blood vessel', 0.47692307692307695, 6.887869297006056, 1.8124524320853552, 'HP:0012372', 'Abnormal eye morphology'),
(107206, 'HP:0007915', 'Polymorphous posterior corneal dystrophy', 'XPO:0102476', 'abnormal lens transitional zone morphology', 0.4473684210526316, 9.014833150514745, 2.0082210218496126, 'UPHENO:0021038', 'abnormal anterior segment of eyeball morphology'),
(107207, 'HP:0007915', 'Polymorphous posterior corneal dystrophy', 'XPO:0127230', 'abnormally localised hyaloid blood vessel', 0.4189189189189189, 6.887869297006056, 1.6986638159319787, 'HP:0012372', 'Abnormal eye morphology'),
(107208, 'HP:0007915', 'Polymorphous posterior corneal dystrophy', 'XPO:0130736', 'increased size of the cornea', 0.4418604651162791, 10.582693223545188, 2.162423120006483, 'UPHENO:0020998', 'abnormal cornea morphology'),
(107209, 'HP:0007915', 'Polymorphous posterior corneal dystrophy', 'XPO:0101817', 'abnormal eye morphology', 0.4246575342465753, 6.887869297006056, 1.7102589253909142, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(107210, 'HP:0007915', 'Polymorphous posterior corneal dystrophy', 'XPO:0100779', 'abnormal optic choroid vascular plexus', 0.4696969696969697, 6.887869297006056, 1.7986693238259617, 'HP:0012372', 'Abnormal eye morphology'),
(107211, 'HP:0007915', 'Polymorphous posterior corneal dystrophy', 'XPO:0130285', 'increased size of the lens transitional zone', 0.40963855421686746, 9.014833150514745, 1.9216719850908865, 'UPHENO:0021038', 'abnormal anterior segment of eyeball morphology'),
