(402774, 'HP:0007515', 'Hypoplastic pilosebaceous units', 'XPO:0128071', 'decreased size of the cell part', 0.4090909090909091, 5.653868323764771, 1.5208373129461366, 'UPHENO:0012541', 'decreased size of the anatomical entity in the independent continuant'),
(402775, 'HP:0007515', 'Hypoplastic pilosebaceous units', 'XPO:0102561', 'abnormal dermis morphology', 0.42, 7.420886955069779, 1.7654383368244009, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(402776, 'HP:0007515', 'Hypoplastic pilosebaceous units', 'XPO:0128502', 'decreased size of the anatomical line', 0.43243243243243246, 5.653868323764771, 1.5636227268424692, 'UPHENO:0012541', 'decreased size of the anatomical entity in the independent continuant'),
(402777, 'HP:0007515', 'Hypoplastic pilosebaceous units', 'XPO:0128960', 'decreased size of the granular gland', 0.42105263157894735, 7.420886955069779, 1.7676492811307372, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(402778, 'HP:0007515', 'Hypoplastic pilosebaceous units', 'XPO:0129230', 'decreased size of the stratum spongiosum', 0.42857142857142855, 7.420886955069779, 1.7833620281931915, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(402779, 'HP:0007515', 'Hypoplastic pilosebaceous units', 'XPO:0102910', 'abnormal pigment cell morphology', 0.40384615384615385, 7.420886955069779, 1.7311547172139254, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(402780, 'HP:0007515', 'Hypoplastic pilosebaceous units', 'XPO:0102176', 'abnormal neuromast support cell morphology', 0.40384615384615385, 7.420886955069779, 1.7311547172139254, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(402781, 'HP:0007515', 'Hypoplastic pilosebaceous units', 'XPO:0128513', 'decreased size of the Eberth-Kastschenko layer', 0.42857142857142855, 7.420886955069779, 1.7833620281931915, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(402782, 'HP:0007515', 'Hypoplastic pilosebaceous units', 'XPO:0102945', 'abnormal Eberth-Kastschenko layer morphology', 0.40384615384615385, 7.420886955069779, 1.7311547172139254, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(402783, 'HP:0007515', 'Hypoplastic pilosebaceous units', 'XPO:0102626', 'abnormal granular gland morphology', 0.4117647058823529, 7.420886955069779, 1.7480444314835069, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(402784, 'HP:0007515', 'Hypoplastic pilosebaceous units', 'XPO:0102840', 'abnormal stratum spongiosum morphology', 0.40384615384615385, 7.420886955069779, 1.7311547172139254, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(402785, 'HP:0007515', 'Hypoplastic pilosebaceous units', 'XPO:0102727', 'abnormal skin seromucous gland morphology', 0.4117647058823529, 7.420886955069779, 1.7480444314835069, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(402786, 'HP:0007515', 'Hypoplastic pilosebaceous units', 'XPO:0128803', 'decreased size of the dermis', 0.4444444444444444, 7.420886955069779, 1.8160869968233935, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(402787, 'HP:0007515', 'Hypoplastic pilosebaceous units', 'XPO:0103147', 'abnormal neuromast mantle cell morphology', 0.40384615384615385, 7.420886955069779, 1.7311547172139254, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(402788, 'HP:0007515', 'Hypoplastic pilosebaceous units', 'XPO:0128647', 'decreased size of the stratum compactum', 0.42857142857142855, 7.420886955069779, 1.7833620281931915, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(402789, 'HP:0007515', 'Hypoplastic pilosebaceous units', 'XPO:0128007', 'decreased size of the anatomical structure', 0.43243243243243246, 5.653868323764771, 1.5636227268424692, 'UPHENO:0012541', 'decreased size of the anatomical entity in the independent continuant'),
(402790, 'HP:0007515', 'Hypoplastic pilosebaceous units', 'XPO:0128037', 'decreased size of the anatomical space', 0.41025641025641024, 5.653868323764771, 1.5230022070142124, 'UPHENO:0012541', 'decreased size of the anatomical entity in the independent continuant'),
(402791, 'HP:0030711', 'Hydrocolpos', 'XPO:0140359', 'abnormally necrotic ovary', 0.4166666666666667, 8.550271745852811, 1.8874886032606055, 'UPHENO:0076766', 'abnormal internal female genitalia morphology'),
(402792, 'HP:0030711', 'Hydrocolpos', 'XPO:0125782', 'absent oviduct', 0.42105263157894735, 7.960567433004586, 1.8307970577123633, 'UPHENO:0005170', 'abnormal female reproductive system'),
(402793, 'HP:0030711', 'Hydrocolpos', 'XPO:0102260', 'abnormal primary oogonium morphology', 0.45454545454545453, 8.550271745852811, 1.971417550192202, 'UPHENO:0076766', 'abnormal internal female genitalia morphology'),
(402794, 'HP:0030711', 'Hydrocolpos', 'XPO:0128383', 'decreased size of the female genitalia', 0.45454545454545453, 8.209234828017744, 1.9317014200884415, 'UPHENO:0087974', 'abnormal female reproductive system morphology'),
(402795, 'HP:0030711', 'Hydrocolpos', 'XPO:0125071', 'absent ovary', 0.42857142857142855, 8.550271745852811, 1.9142628285567427, 'UPHENO:0076766', 'abnormal internal female genitalia morphology'),
(402796, 'HP:0030711', 'Hydrocolpos', 'XPO:0127178', 'abnormally localised follicle cell', 0.46153846153846156, 8.550271745852811, 1.9865244190084053, 'UPHENO:0076766', 'abnormal internal female genitalia morphology'),
(402797, 'HP:0030711', 'Hydrocolpos', 'XPO:0100628', 'abnormal primary oogonium', 0.5084745762711864, 8.550271745852811, 2.0850889196808864, 'UPHENO:0076766', 'abnormal internal female genitalia morphology'),
(402798, 'HP:0030711', 'Hydrocolpos', 'XPO:0101262', 'abnormal oviduct', 0.5217391304347826, 7.960567433004586, 2.037974369383301, 'UPHENO:0005170', 'abnormal female reproductive system'),
(402799, 'HP:0030711', 'Hydrocolpos', 'XPO:0139867', 'abnormally necrotic genital system', 0.4489795918367347, 7.005035523447265, 1.7734480511475887, 'UPHENO:0020950', 'abnormal reproductive system morphology'),
(402800, 'HP:0030711', 'Hydrocolpos', 'XPO:0131177', 'abnormally increased number of follicle cell', 0.44776119402985076, 8.550271745852811, 1.9566501696017997, 'UPHENO:0076766', 'abnormal internal female genitalia morphology'),
(402801, 'HP:0030711', 'Hydrocolpos', 'XPO:0129178', 'decreased size of the follicle layer', 0.4411764705882353, 8.550271745852811, 1.9422097495908242, 'UPHENO:0076766', 'abnormal internal female genitalia morphology'),
(402802, 'HP:0030711', 'Hydrocolpos', 'XPO:0129864', 'increased size of the genital system', 0.43137254901960786, 7.005035523447265, 1.7383267902561792, 'HP:0012243', 'Abnormal reproductive system morphology'),
(402803, 'HP:0030711', 'Hydrocolpos', 'XPO:0126899', 'abnormally localised primary oogonium', 0.44776119402985076, 8.550271745852811, 1.9566501696017997, 'UPHENO:0076766', 'abnormal internal female genitalia morphology'),
(402804, 'HP:0030711', 'Hydrocolpos', 'XPO:0126166', 'absent follicle layer', 0.45454545454545453, 8.550271745852811, 1.971417550192202, 'UPHENO:0076766', 'abnormal internal female genitalia morphology'),
(402805, 'HP:0030711', 'Hydrocolpos', 'XPO:0127432', 'abnormally localised oviduct', 0.43636363636363634, 7.960567433004586, 1.86378704593197, 'UPHENO:0005170', 'abnormal female reproductive system'),
(402806, 'HP:0030711', 'Hydrocolpos', 'XPO:0128384', 'decreased size of the genital system', 0.43137254901960786, 7.005035523447265, 1.7383267902561792, 'UPHENO:0020950', 'abnormal reproductive system morphology'),
(402807, 'HP:0030711', 'Hydrocolpos', 'XPO:0128607', 'decreased size of the oviduct', 0.423728813559322, 8.209234828017744, 1.8650708656525155, 'UPHENO:0087974', 'abnormal female reproductive system morphology'),
(402808, 'HP:0030711', 'Hydrocolpos', 'XPO:0100765', 'abnormal male genitalia', 0.5, 7.005035523447265, 1.8715014725411339, 'HP:0012243', 'Abnormal reproductive system morphology'),
(402809, 'HP:0030711', 'Hydrocolpos', 'XPO:0140069', 'abnormally necrotic follicle layer', 0.45454545454545453, 8.550271745852811, 1.971417550192202, 'UPHENO:0076766', 'abnormal internal female genitalia morphology'),
(402810, 'HP:0030711', 'Hydrocolpos', 'XPO:0131395', 'abnormally decreased number of follicle cell', 0.43478260869565216, 8.550271745852811, 1.9280844003099589, 'UPHENO:0076766', 'abnormal internal female genitalia morphology'),
(402811, 'HP:0030711', 'Hydrocolpos', 'XPO:0102596', 'abnormal follicle layer morphology', 0.4918032786885246, 8.550271745852811, 2.0506222661154023, 'UPHENO:0076766', 'abnormal internal female genitalia morphology'),
(402812, 'HP:0030711', 'Hydrocolpos', 'XPO:0102894', 'abnormal oviduct morphology', 0.49019607843137253, 8.209234828017744, 2.006024605934967, 'UPHENO:0087974', 'abnormal female reproductive system morphology'),
(402813, 'HP:0030711', 'Hydrocolpos', 'XPO:0100278', 'abnormal follicle cell', 0.5172413793103449, 8.550271745852811, 2.1029870069268566, 'UPHENO:0076766', 'abnormal internal female genitalia morphology'),
(402814, 'HP:0030711', 'Hydrocolpos', 'XPO:0125139', 'absent male genitalia', 0.4074074074074074, 7.005035523447265, 1.689349981917436, 'HP:0012243', 'Abnormal reproductive system morphology'),
(402815, 'HP:0030711', 'Hydrocolpos', 'XPO:0127828', 'abnormally localised follicle layer', 0.46153846153846156, 8.550271745852811, 1.9865244190084053, 'UPHENO:0076766', 'abnormal internal female genitalia morphology'),
(402816, 'HP:0030711', 'Hydrocolpos', 'XPO:0102864', 'abnormal female genitalia morphology', 0.5319148936170213, 8.209234828017744, 2.089644532025053, 'UPHENO:0087974', 'abnormal female reproductive system morphology'),
(402817, 'HP:0030711', 'Hydrocolpos', 'XPO:0102270', 'abnormal polar body morphology', 0.4489795918367347, 7.005035523447265, 1.7734480511475887, 'UPHENO:0020950', 'abnormal reproductive system morphology'),
(402818, 'HP:0030711', 'Hydrocolpos', 'XPO:0102397', 'abnormal male genitalia morphology', 0.44, 7.005035523447265, 1.755624000267938, 'UPHENO:0020950', 'abnormal reproductive system morphology'),
(402819, 'HP:0030711', 'Hydrocolpos', 'XPO:0101910', 'abnormal follicle cell morphology', 0.46875, 8.550271745852811, 2.0019839861668487, 'UPHENO:0076766', 'abnormal internal female genitalia morphology'),
(402820, 'HP:0030711', 'Hydrocolpos', 'XPO:0140488', 'abnormally necrotic primary oogonium', 0.4225352112676056, 8.550271745852811, 1.9007342998245065, 'UPHENO:0076766', 'abnormal internal female genitalia morphology'),
(402821, 'HP:0030711', 'Hydrocolpos', 'XPO:0141148', 'abnormally necrotic oviduct', 0.43859649122807015, 8.209234828017744, 1.897509312555765, 'UPHENO:0087974', 'abnormal female reproductive system morphology'),
(402822, 'HP:0030711', 'Hydrocolpos', 'XPO:0130654', 'increased size of the follicle layer', 0.4411764705882353, 8.550271745852811, 1.9422097495908242, 'UPHENO:0076766', 'abnormal internal female genitalia morphology'),
(402823, 'HP:0030711', 'Hydrocolpos', 'XPO:0126964', 'abnormally localised female genitalia', 0.47058823529411764, 7.960567433004586, 1.9354971919993715, 'UPHENO:0005170', 'abnormal female reproductive system'),
(402824, 'HP:0030711', 'Hydrocolpos', 'XPO:0131086', 'abnormally increased number of primary oogonium', 0.43478260869565216, 8.550271745852811, 1.9280844003099589, 'UPHENO:0076766', 'abnormal internal female genitalia morphology'),
(402825, 'HP:0030711', 'Hydrocolpos', 'XPO:0130087', 'increased size of the oviduct', 0.423728813559322, 8.209234828017744, 1.8650708656525155, 'UPHENO:0087974', 'abnormal female reproductive system morphology'),
(402826, 'HP:0030711', 'Hydrocolpos', 'XPO:0125335', 'absent female genitalia', 0.46153846153846156, 7.960567433004586, 1.9167962974719344, 'UPHENO:0005170', 'abnormal female reproductive system'),
(402827, 'HP:0030711', 'Hydrocolpos', 'XPO:0129863', 'increased size of the female genitalia', 0.45454545454545453, 8.209234828017744, 1.9317014200884415, 'UPHENO:0087974', 'abnormal female reproductive system morphology'),
(402828, 'HP:0030711', 'Hydrocolpos', 'XPO:0141099', 'abnormally necrotic follicle cell', 0.4411764705882353, 8.550271745852811, 1.9422097495908242, 'UPHENO:0076766', 'abnormal internal female genitalia morphology'),
(402829, 'HP:0030711', 'Hydrocolpos', 'XPO:0100036', 'abnormal ovary', 0.5555555555555556, 8.550271745852811, 2.179484106369723, 'UPHENO:0076766', 'abnormal internal female genitalia morphology'),
(402830, 'HP:0030711', 'Hydrocolpos', 'XPO:0126691', 'abnormally localised ovary', 0.44776119402985076, 8.550271745852811, 1.9566501696017997, 'UPHENO:0076766', 'abnormal internal female genitalia morphology'),
(402831, 'HP:0030711', 'Hydrocolpos', 'XPO:0101232', 'abnormal female genitalia', 0.5714285714285714, 7.960567433004586, 2.1328140275238767, 'UPHENO:0005170', 'abnormal female reproductive system'),
(402832, 'HP:0030711', 'Hydrocolpos', 'XPO:0100964', 'abnormal follicle layer', 0.5357142857142857, 8.550271745852811, 2.1402109057269514, 'UPHENO:0076766', 'abnormal internal female genitalia morphology'),
(402833, 'HP:0030711', 'Hydrocolpos', 'XPO:0101752', 'abnormal genital system morphology', 0.5, 7.005035523447265, 1.8715014725411339, 'HP:0012243', 'Abnormal reproductive system morphology'),
(402834, 'HP:0030711', 'Hydrocolpos', 'XPO:0126762', 'abnormally localised male genitalia', 0.41509433962264153, 7.005035523447265, 1.705212771075354, 'HP:0012243', 'Abnormal reproductive system morphology'),
(402835, 'HP:0030711', 'Hydrocolpos', 'XPO:0125273', 'absent primary oogonium', 0.42857142857142855, 8.550271745852811, 1.9142628285567427, 'UPHENO:0076766', 'abnormal internal female genitalia morphology'),
(402836, 'HP:0030711', 'Hydrocolpos', 'XPO:0125540', 'absent follicle cell', 0.4411764705882353, 8.550271745852811, 1.9422097495908242, 'UPHENO:0076766', 'abnormal internal female genitalia morphology'),
(402837, 'HP:0030711', 'Hydrocolpos', 'XPO:0101668', 'abnormal ovary morphology', 0.46875, 8.550271745852811, 2.0019839861668487, 'UPHENO:0076766', 'abnormal internal female genitalia morphology'),
(402838, 'HP:0030711', 'Hydrocolpos', 'XPO:0140839', 'abnormally necrotic female genitalia', 0.4716981132075472, 8.209234828017744, 1.967811113713319, 'UPHENO:0087974', 'abnormal female reproductive system morphology'),
(402839, 'HP:0030711', 'Hydrocolpos', 'XPO:0100414', 'abnormal testis', 0.4074074074074074, 7.005035523447265, 1.689349981917436, 'HP:0012243', 'Abnormal reproductive system morphology'),
(402840, 'HP:0030711', 'Hydrocolpos', 'XPO:0140723', 'abnormally necrotic polar body', 0.41509433962264153, 7.005035523447265, 1.705212771075354, 'UPHENO:0020950', 'abnormal reproductive system morphology'),
(402841, 'HP:0030711', 'Hydrocolpos', 'XPO:0131304', 'abnormally decreased number of primary oogonium', 0.4225352112676056, 8.550271745852811, 1.9007342998245065, 'UPHENO:0076766', 'abnormal internal female genitalia morphology'),
(402842, 'HP:0005441', 'Sclerotic cranial sutures', 'XPO:0103358', 'decreased size of the pharyngeal region', 0.42, 4.5318002188002176, 1.3796217205799897, 'UPHENO:0087907', 'abnormal head morphology'),
(402843, 'HP:0005441', 'Sclerotic cranial sutures', 'XPO:0100226', 'abnormal vertebral element', 0.4107142857142857, 6.272837960958401, 1.6050994245019483, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(402844, 'HP:0005441', 'Sclerotic cranial sutures', 'XPO:0100584', 'abnormal vertebral column', 0.46, 6.272837960958401, 1.69867756270602, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(402845, 'HP:0005441', 'Sclerotic cranial sutures', 'XPO:0100693', 'abnormal vertebral centrum', 0.40350877192982454, 6.272837960958401, 1.5909573036826314, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(402846, 'HP:0005441', 'Sclerotic cranial sutures', 'XPO:0140223', 'abnormally necrotic head region', 0.4117647058823529, 4.5318002188002176, 1.3660290568695288, 'UPHENO:0087907', 'abnormal head morphology'),
(402847, 'HP:0005441', 'Sclerotic cranial sutures', 'XPO:0101634', 'abnormal head morphology', 0.45652173913043476, 4.5318002188002176, 1.4383550734357495, 'UPHENO:0087907', 'abnormal head morphology'),
(402848, 'HP:0005441', 'Sclerotic cranial sutures', 'XPO:0141061', 'abnormally necrotic suspensorium', 0.4406779661016949, 4.638757693672553, 1.4297546312868548, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(402849, 'HP:0005441', 'Sclerotic cranial sutures', 'XPO:0102485', 'abnormal osseous labyrinth morphology', 0.41333333333333333, 7.024697770424301, 1.7039782114536297, 'HP:0000929', 'Abnormal skull morphology'),
(402850, 'HP:0005441', 'Sclerotic cranial sutures', 'XPO:0130358', 'increased size of the lower jaw', 0.40789473684210525, 7.024697770424301, 1.6927307076031153, 'HP:0000929', 'Abnormal skull morphology'),
(402851, 'HP:0005441', 'Sclerotic cranial sutures', 'XPO:0139715', 'abnormally necrotic head', 0.4117647058823529, 4.5318002188002176, 1.3660290568695288, 'UPHENO:0087907', 'abnormal head morphology'),
(402852, 'HP:0005441', 'Sclerotic cranial sutures', 'XPO:0129688', 'increased size of the olfactory region', 0.5, 7.024697770424301, 1.8741261657669024, 'HP:0000929', 'Abnormal skull morphology'),
(402853, 'HP:0005441', 'Sclerotic cranial sutures', 'XPO:0141719', 'abnormal anterior notochord morphology', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(402854, 'HP:0005441', 'Sclerotic cranial sutures', 'XPO:0102567', 'abnormal skeleton morphology', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(402855, 'HP:0005441', 'Sclerotic cranial sutures', 'XPO:0128238', 'decreased size of the ethmoid region', 0.43333333333333335, 4.638757693672553, 1.4177899470389728, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(402856, 'HP:0005441', 'Sclerotic cranial sutures', 'XPO:0103101', 'abnormal medial nasal prominence morphology', 0.42857142857142855, 4.5318002188002176, 1.3936283915633758, 'UPHENO:0087907', 'abnormal head morphology'),
(402857, 'HP:0005441', 'Sclerotic cranial sutures', 'XPO:0102144', 'abnormal cranial skeleton morphology', 0.40384615384615385, 6.211345574613551, 1.5838017617482976, 'UPHENO:0087089', 'abnormal axial skeleton plus cranial skeleton morphology'),
(402858, 'HP:0005441', 'Sclerotic cranial sutures', 'XPO:0139832', 'abnormally necrotic splanchnocranium', 0.43333333333333335, 4.638757693672553, 1.4177899470389728, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(402859, 'HP:0005441', 'Sclerotic cranial sutures', 'XPO:0102572', 'abnormal hatching gland primordium morphology', 0.4117647058823529, 4.5318002188002176, 1.3660290568695288, 'UPHENO:0087907', 'abnormal head morphology'),
(402860, 'HP:0005441', 'Sclerotic cranial sutures', 'XPO:0129513', 'increased size of the splanchnocranium', 0.41935483870967744, 4.638757693672553, 1.394734915474381, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(402861, 'HP:0005441', 'Sclerotic cranial sutures', 'XPO:0102921', 'abnormal orbital region morphology', 0.5, 7.024697770424301, 1.8741261657669024, 'HP:0000929', 'Abnormal skull morphology'),
(402862, 'HP:0005441', 'Sclerotic cranial sutures', 'XPO:0129406', 'decreased size of the suspensorium', 0.4262295081967213, 4.638757693672553, 1.4061206955371255, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(402863, 'HP:0005441', 'Sclerotic cranial sutures', 'XPO:0140335', 'abnormally necrotic pharyngeal region', 0.4375, 4.5318002188002176, 1.4080705222839853, 'UPHENO:0087907', 'abnormal head morphology'),
(402864, 'HP:0005441', 'Sclerotic cranial sutures', 'XPO:0139784', 'abnormally necrotic cranium', 0.45614035087719296, 4.638757693672553, 1.4546217934659431, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(402865, 'HP:0005441', 'Sclerotic cranial sutures', 'XPO:0103176', 'abnormal fenestra basicranialis morphology', 0.49056603773584906, 4.638757693672553, 1.508514826510376, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(402866, 'HP:0005441', 'Sclerotic cranial sutures', 'XPO:0130138', 'increased size of the braincase and otic capsule skeleton', 0.40625, 4.638757693672553, 1.3727692133255593, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(402867, 'HP:0005441', 'Sclerotic cranial sutures', 'XPO:0140926', 'abnormally necrotic neurocranium', 0.5166666666666667, 7.024697770424301, 1.9051055564944135, 'HP:0000929', 'Abnormal skull morphology'),
(402868, 'HP:0005441', 'Sclerotic cranial sutures', 'XPO:0130147', 'increased size of the fenestra basicranialis', 0.4482758620689655, 4.638757693672553, 1.4420274283314136, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(402869, 'HP:0005441', 'Sclerotic cranial sutures', 'XPO:0101659', 'abnormal lower jaw morphology', 0.4492753623188406, 7.024697770424301, 1.7765200916363793, 'HP:0000929', 'Abnormal skull morphology'),
(402870, 'HP:0005441', 'Sclerotic cranial sutures', 'XPO:0140914', 'abnormally necrotic intercanthal region', 0.4117647058823529, 4.5318002188002176, 1.3660290568695288, 'UPHENO:0087907', 'abnormal head morphology'),
(402871, 'HP:0005441', 'Sclerotic cranial sutures', 'XPO:0102776', 'abnormal fenestra subocularis morphology', 0.49056603773584906, 4.638757693672553, 1.508514826510376, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(402872, 'HP:0005441', 'Sclerotic cranial sutures', 'XPO:0140897', 'abnormally necrotic lower jaw', 0.4189189189189189, 7.024697770424301, 1.7154529418548001, 'HP:0000929', 'Abnormal skull morphology'),
(402873, 'HP:0005441', 'Sclerotic cranial sutures', 'XPO:0129957', 'increased size of the neurocranium', 0.49206349206349204, 7.024697770424301, 1.8591926515575539, 'HP:0000929', 'Abnormal skull morphology'),
(402874, 'HP:0005441', 'Sclerotic cranial sutures', 'XPO:0129514', 'increased size of the cranium', 0.4406779661016949, 4.638757693672553, 1.4297546312868548, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(402875, 'HP:0005441', 'Sclerotic cranial sutures', 'XPO:0102538', 'abnormal lateral nasal prominence morphology', 0.42857142857142855, 4.5318002188002176, 1.3936283915633758, 'UPHENO:0087907', 'abnormal head morphology'),
(402876, 'HP:0005441', 'Sclerotic cranial sutures', 'XPO:0128947', 'decreased size of the otic region', 0.5, 7.024697770424301, 1.8741261657669024, 'HP:0000929', 'Abnormal skull morphology'),
(402877, 'HP:0005441', 'Sclerotic cranial sutures', 'XPO:0128208', 'decreased size of the olfactory region', 0.5, 7.024697770424301, 1.8741261657669024, 'HP:0000929', 'Abnormal skull morphology'),
(402878, 'HP:0005441', 'Sclerotic cranial sutures', 'XPO:0102828', 'abnormal occipital region morphology', 0.5740740740740741, 7.024697770424301, 2.008157580521644, 'HP:0000929', 'Abnormal skull morphology'),
(402879, 'HP:0005441', 'Sclerotic cranial sutures', 'XPO:0103152', 'abnormal otic region morphology', 0.5636363636363636, 7.024697770424301, 1.9898178577363366, 'HP:0000929', 'Abnormal skull morphology'),
(402880, 'HP:0005441', 'Sclerotic cranial sutures', 'XPO:0141835', 'edematous head', 0.4375, 4.5318002188002176, 1.4080705222839853, 'UPHENO:0087907', 'abnormal head morphology'),
(402881, 'HP:0005441', 'Sclerotic cranial sutures', 'XPO:0102665', 'abnormal suspensorium morphology', 0.48148148148148145, 4.638757693672553, 1.4944818254442178, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(402882, 'HP:0005441', 'Sclerotic cranial sutures', 'XPO:0102401', 'abnormal neurocranium morphology', 0.5636363636363636, 7.024697770424301, 1.9898178577363366, 'HP:0000929', 'Abnormal skull morphology'),
(402883, 'HP:0005441', 'Sclerotic cranial sutures', 'XPO:0141839', 'edematous pharyngeal region', 0.44680851063829785, 4.5318002188002176, 1.422971154406314, 'UPHENO:0087907', 'abnormal head morphology'),
(402884, 'HP:0005441', 'Sclerotic cranial sutures', 'XPO:0140644', 'abnormally necrotic otic region', 0.5166666666666667, 7.024697770424301, 1.9051055564944135, 'HP:0000929', 'Abnormal skull morphology'),
(402885, 'HP:0005441', 'Sclerotic cranial sutures', 'XPO:0102010', 'abnormal perichondrium morphology', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(402886, 'HP:0005441', 'Sclerotic cranial sutures', 'XPO:0102804', 'abnormal pharyngeal pouch morphology', 0.42857142857142855, 4.5318002188002176, 1.3936283915633758, 'UPHENO:0087907', 'abnormal head morphology'),
(402887, 'HP:0005441', 'Sclerotic cranial sutures', 'XPO:0102734', 'abnormal craniofacial region morphology', 0.42857142857142855, 4.5318002188002176, 1.3936283915633758, 'UPHENO:0087907', 'abnormal head morphology'),
(402888, 'HP:0005441', 'Sclerotic cranial sutures', 'XPO:0101860', 'abnormal skeletal subdivision morphology', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(402889, 'HP:0005441', 'Sclerotic cranial sutures', 'XPO:0102720', 'abnormal dermatocranium morphology', 0.48148148148148145, 4.638757693672553, 1.4944818254442178, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(402890, 'HP:0005441', 'Sclerotic cranial sutures', 'XPO:0128846', 'decreased size of the choana', 0.4696969696969697, 7.024697770424301, 1.8164468766813286, 'HP:0000929', 'Abnormal skull morphology'),
(402891, 'HP:0005441', 'Sclerotic cranial sutures', 'XPO:0102082', 'abnormal circumpharyngeal ridge morphology', 0.42, 4.5318002188002176, 1.3796217205799897, 'UPHENO:0087907', 'abnormal head morphology'),
(402892, 'HP:0005441', 'Sclerotic cranial sutures', 'XPO:0103707', 'increased pigmentation in the head', 0.42857142857142855, 4.5318002188002176, 1.3936283915633758, 'UPHENO:0087907', 'abnormal head morphology'),
(402893, 'HP:0005441', 'Sclerotic cranial sutures', 'XPO:0130767', 'increased size of the orbital region', 0.43661971830985913, 7.024697770424301, 1.7513199484202062, 'HP:0000929', 'Abnormal skull morphology'),
(402894, 'HP:0005441', 'Sclerotic cranial sutures', 'XPO:0102054', 'abnormal notochord morphology', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(402895, 'HP:0005441', 'Sclerotic cranial sutures', 'XPO:0103721', 'increased size of the chondrocranium', 0.41935483870967744, 4.638757693672553, 1.394734915474381, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(402896, 'HP:0005441', 'Sclerotic cranial sutures', 'XPO:0130880', 'increased size of the suspensorium', 0.4262295081967213, 4.638757693672553, 1.4061206955371255, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(402897, 'HP:0005441', 'Sclerotic cranial sutures', 'XPO:0128659', 'decreased size of the braincase and otic capsule skeleton', 0.40625, 4.638757693672553, 1.3727692133255593, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(402898, 'HP:0005441', 'Sclerotic cranial sutures', 'XPO:0129771', 'increased size of the dermatocranium', 0.41935483870967744, 4.638757693672553, 1.394734915474381, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(402899, 'HP:0005441', 'Sclerotic cranial sutures', 'XPO:0140639', 'abnormally necrotic upper jaw', 0.40789473684210525, 7.024697770424301, 1.6927307076031153, 'HP:0000929', 'Abnormal skull morphology'),
(402900, 'HP:0005441', 'Sclerotic cranial sutures', 'XPO:0141201', 'abnormally necrotic sphenoid region', 0.5166666666666667, 7.024697770424301, 1.9051055564944135, 'HP:0000929', 'Abnormal skull morphology'),
(402901, 'HP:0005441', 'Sclerotic cranial sutures', 'XPO:0102215', 'abnormal mandibular arch skeleton morphology', 0.45614035087719296, 4.638757693672553, 1.4546217934659431, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(402902, 'HP:0005441', 'Sclerotic cranial sutures', 'XPO:0141298', 'abnormal intercanthal region morphology', 0.4375, 4.5318002188002176, 1.4080705222839853, 'UPHENO:0087907', 'abnormal head morphology'),
(402903, 'HP:0005441', 'Sclerotic cranial sutures', 'XPO:0129689', 'increased size of the sphenoid region', 0.5, 7.024697770424301, 1.8741261657669024, 'HP:0000929', 'Abnormal skull morphology'),
(402904, 'HP:0005441', 'Sclerotic cranial sutures', 'XPO:0103332', 'decreased size of the chondrocranium', 0.41935483870967744, 4.638757693672553, 1.394734915474381, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(402905, 'HP:0005441', 'Sclerotic cranial sutures', 'XPO:0128880', 'decreased size of the lower jaw', 0.40789473684210525, 7.024697770424301, 1.6927307076031153, 'HP:0000929', 'Abnormal skull morphology'),
(402906, 'HP:0005441', 'Sclerotic cranial sutures', 'XPO:0128209', 'decreased size of the sphenoid region', 0.5, 7.024697770424301, 1.8741261657669024, 'HP:0000929', 'Abnormal skull morphology'),
(402907, 'HP:0005441', 'Sclerotic cranial sutures', 'XPO:0140560', 'abnormally necrotic orbital region', 0.4626865671641791, 7.024697770424301, 1.8028403414510898, 'HP:0000929', 'Abnormal skull morphology'),
(402908, 'HP:0005441', 'Sclerotic cranial sutures', 'XPO:0103739', 'increased size of the pharyngeal region', 0.42, 4.5318002188002176, 1.3796217205799897, 'UPHENO:0087907', 'abnormal head morphology'),
(402909, 'HP:0005441', 'Sclerotic cranial sutures', 'XPO:0103381', 'increased size of the head', 0.5344827586206896, 7.024697770424301, 1.9376738226061134, 'HP:0000929', 'Abnormal skull morphology'),
(402910, 'HP:0005441', 'Sclerotic cranial sutures', 'XPO:0141193', 'abnormally necrotic mandibular arch skeleton', 0.4126984126984127, 4.638757693672553, 1.3836213127410304, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(402911, 'HP:0005441', 'Sclerotic cranial sutures', 'XPO:0102351', 'abnormal sphenoid region morphology', 0.5636363636363636, 7.024697770424301, 1.9898178577363366, 'HP:0000929', 'Abnormal skull morphology'),
(402912, 'HP:0005441', 'Sclerotic cranial sutures', 'XPO:0141339', 'decreased pigmentation in the head', 0.42857142857142855, 4.5318002188002176, 1.3936283915633758, 'UPHENO:0087907', 'abnormal head morphology'),
(402913, 'HP:0005441', 'Sclerotic cranial sutures', 'XPO:0141185', 'abnormally necrotic occipital region', 0.5254237288135594, 7.024697770424301, 1.9211826816637279, 'HP:0000929', 'Abnormal skull morphology'),
(402914, 'HP:0005441', 'Sclerotic cranial sutures', 'XPO:0128971', 'decreased size of the fenestra subocularis', 0.4482758620689655, 4.638757693672553, 1.4420274283314136, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(402915, 'HP:0005441', 'Sclerotic cranial sutures', 'XPO:0129718', 'increased size of the ethmoid region', 0.43333333333333335, 4.638757693672553, 1.4177899470389728, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(402916, 'HP:0005441', 'Sclerotic cranial sutures', 'XPO:0140672', 'abnormally necrotic olfactory region', 0.5166666666666667, 7.024697770424301, 1.9051055564944135, 'HP:0000929', 'Abnormal skull morphology'),
(402917, 'HP:0005441', 'Sclerotic cranial sutures', 'XPO:0115586', 'abnormally decreased volume of chondrocranium', 0.40625, 4.638757693672553, 1.3727692133255593, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(402918, 'HP:0005441', 'Sclerotic cranial sutures', 'XPO:0100420', 'abnormal choana', 0.4444444444444444, 4.5318002188002176, 1.4192016877730502, 'UPHENO:0087907', 'abnormal head morphology'),
(402919, 'HP:0005441', 'Sclerotic cranial sutures', 'XPO:0102806', 'abnormal articular system morphology', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(402920, 'HP:0005441', 'Sclerotic cranial sutures', 'XPO:0102272', 'abnormal notochordal sheath morphology', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(402921, 'HP:0005441', 'Sclerotic cranial sutures', 'XPO:0142059', 'abnormal nasal region morphology', 0.44680851063829785, 4.5318002188002176, 1.422971154406314, 'UPHENO:0087907', 'abnormal head morphology'),
(402922, 'HP:0005441', 'Sclerotic cranial sutures', 'XPO:0102564', 'abnormal olfactory region morphology', 0.5636363636363636, 7.024697770424301, 1.9898178577363366, 'HP:0000929', 'Abnormal skull morphology'),
(402923, 'HP:0005441', 'Sclerotic cranial sutures', 'XPO:0101764', 'abnormal cranium morphology', 0.5, 4.638757693672553, 1.5229507040072823, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(402924, 'HP:0005441', 'Sclerotic cranial sutures', 'XPO:0128033', 'decreased size of the splanchnocranium', 0.41935483870967744, 4.638757693672553, 1.394734915474381, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(402925, 'HP:0005441', 'Sclerotic cranial sutures', 'XPO:0139745', 'abnormally necrotic chondrocranium', 0.43333333333333335, 4.638757693672553, 1.4177899470389728, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(402926, 'HP:0005441', 'Sclerotic cranial sutures', 'XPO:0128291', 'decreased size of the dermatocranium', 0.41935483870967744, 4.638757693672553, 1.394734915474381, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(402927, 'HP:0005441', 'Sclerotic cranial sutures', 'XPO:0129291', 'decreased size of the orbital region', 0.43661971830985913, 7.024697770424301, 1.7513199484202062, 'HP:0000929', 'Abnormal skull morphology'),
(402928, 'HP:0005441', 'Sclerotic cranial sutures', 'XPO:0128668', 'decreased size of the fenestra basicranialis', 0.4482758620689655, 4.638757693672553, 1.4420274283314136, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(402929, 'HP:0005441', 'Sclerotic cranial sutures', 'XPO:0139775', 'abnormally necrotic braincase and otic capsule skeleton', 0.41935483870967744, 4.638757693672553, 1.394734915474381, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(402930, 'HP:0005441', 'Sclerotic cranial sutures', 'XPO:0101681', 'abnormal chondrocranium morphology', 0.48148148148148145, 4.638757693672553, 1.4944818254442178, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(402931, 'HP:0005441', 'Sclerotic cranial sutures', 'XPO:0128034', 'decreased size of the cranium', 0.4406779661016949, 4.638757693672553, 1.4297546312868548, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(402932, 'HP:0005441', 'Sclerotic cranial sutures', 'XPO:0107372', 'abnormal flexural organ morphology', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(402933, 'HP:0005441', 'Sclerotic cranial sutures', 'XPO:0102795', 'abnormal branchial basket morphology', 0.40625, 4.638757693672553, 1.3727692133255593, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(402934, 'HP:0005441', 'Sclerotic cranial sutures', 'XPO:0130425', 'increased size of the otic region', 0.5, 7.024697770424301, 1.8741261657669024, 'HP:0000929', 'Abnormal skull morphology'),
(402935, 'HP:0005441', 'Sclerotic cranial sutures', 'XPO:0130324', 'increased size of the choana', 0.4696969696969697, 7.024697770424301, 1.8164468766813286, 'HP:0000929', 'Abnormal skull morphology'),
(402936, 'HP:0005441', 'Sclerotic cranial sutures', 'XPO:0101997', 'abnormal braincase and otic capsule skeleton morphology', 0.4642857142857143, 4.638757693672553, 1.4675520192501232, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(402937, 'HP:0005441', 'Sclerotic cranial sutures', 'XPO:0140132', 'abnormally necrotic ethmoid region', 0.4482758620689655, 4.638757693672553, 1.4420274283314136, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(402938, 'HP:0005441', 'Sclerotic cranial sutures', 'XPO:0102052', 'abnormal choana morphology', 0.5166666666666667, 7.024697770424301, 1.9051055564944135, 'HP:0000929', 'Abnormal skull morphology'),
(402939, 'HP:0005441', 'Sclerotic cranial sutures', 'XPO:0102216', 'abnormal vertebral column morphology', 0.4107142857142857, 6.272837960958401, 1.6050994245019483, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(402940, 'HP:0005441', 'Sclerotic cranial sutures', 'XPO:0139880', 'abnormally necrotic dermatocranium', 0.43333333333333335, 4.638757693672553, 1.4177899470389728, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(402941, 'HP:0005441', 'Sclerotic cranial sutures', 'XPO:0103138', 'abnormal upper jaw morphology', 0.43661971830985913, 7.024697770424301, 1.7513199484202062, 'HP:0000929', 'Abnormal skull morphology'),
(402942, 'HP:0005441', 'Sclerotic cranial sutures', 'XPO:0102005', 'abnormal splanchnocranium morphology', 0.48148148148148145, 4.638757693672553, 1.4944818254442178, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(402943, 'HP:0005441', 'Sclerotic cranial sutures', 'XPO:0128477', 'decreased size of the neurocranium', 0.49206349206349204, 7.024697770424301, 1.8591926515575539, 'HP:0000929', 'Abnormal skull morphology'),
(402944, 'HP:0005441', 'Sclerotic cranial sutures', 'XPO:0141829', 'increased width of head', 0.5, 7.024697770424301, 1.8741261657669024, 'HP:0000929', 'Abnormal skull morphology'),
(402945, 'HP:0005441', 'Sclerotic cranial sutures', 'XPO:0128905', 'decreased size of the occipital region', 0.5081967213114754, 7.024697770424301, 1.8894254087244782, 'HP:0000929', 'Abnormal skull morphology'),
(402946, 'HP:0005441', 'Sclerotic cranial sutures', 'XPO:0102097', 'abnormal skeletal system morphology', 0.43478260869565216, 4.638757693672553, 1.4201588541997616, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(402947, 'HP:0005441', 'Sclerotic cranial sutures', 'XPO:0101957', 'abnormal axial skeleton morphology', 0.4117647058823529, 6.211345574613551, 1.599253852164941, 'UPHENO:0087089', 'abnormal axial skeleton plus cranial skeleton morphology'),
(402948, 'HP:0005441', 'Sclerotic cranial sutures', 'XPO:0115526', 'abnormally incomplete structure of head', 0.44680851063829785, 4.5318002188002176, 1.422971154406314, 'UPHENO:0087907', 'abnormal head morphology'),
(402949, 'HP:0005441', 'Sclerotic cranial sutures', 'XPO:0102461', 'abnormal postcranial axial skeleton morphology', 0.4423076923076923, 6.272837960958401, 1.6656903922192745, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(402950, 'HP:0005441', 'Sclerotic cranial sutures', 'XPO:0130449', 'increased size of the fenestra subocularis', 0.4482758620689655, 4.638757693672553, 1.4420274283314136, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(402951, 'HP:0005441', 'Sclerotic cranial sutures', 'XPO:0130383', 'increased size of the occipital region', 0.5081967213114754, 7.024697770424301, 1.8894254087244782, 'HP:0000929', 'Abnormal skull morphology'),
(402952, 'HP:0005441', 'Sclerotic cranial sutures', 'XPO:0102217', 'abnormal elastica externa morphology', 0.43478260869565216, 4.638757693672553, 1.4201588541997616, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(402953, 'HP:0005441', 'Sclerotic cranial sutures', 'XPO:0141723', 'abnormal posterior notochord morphology', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(402954, 'HP:0005441', 'Sclerotic cranial sutures', 'XPO:0102259', 'abnormal pharyngeal region morphology', 0.4666666666666667, 4.5318002188002176, 1.4542489821577214, 'UPHENO:0087907', 'abnormal head morphology'),
(402955, 'HP:0005441', 'Sclerotic cranial sutures', 'XPO:0102092', 'abnormal ethmoid region morphology', 0.49056603773584906, 4.638757693672553, 1.508514826510376, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(402956, 'HP:0011540', 'Congenitally corrected transposition of the great arteries', 'XPO:0139730', 'abnormally necrotic vein', 0.40350877192982454, 7.803720102857406, 1.7745054283343504, 'HP:0033353', 'Abnormal blood vessel morphology'),
(402957, 'HP:0011540', 'Congenitally corrected transposition of the great arteries', 'XPO:0102412', 'abnormal vascular plexus morphology', 0.4489795918367347, 6.974839882869777, 1.7696216442328712, 'UPHENO:0087186', 'abnormal blood vessel morphology'),
(402958, 'HP:0011540', 'Congenitally corrected transposition of the great arteries', 'XPO:0101675', 'abnormal vein morphology', 0.45098039215686275, 7.803720102857406, 1.8759863411733644, 'HP:0033353', 'Abnormal blood vessel morphology'),
(402959, 'HP:0011540', 'Congenitally corrected transposition of the great arteries', 'XPO:0102838', 'abnormal ischiadic vein morphology', 0.4339622641509434, 7.803720102857406, 1.8402499951463749, 'HP:0033353', 'Abnormal blood vessel morphology'),
(402960, 'HP:0011540', 'Congenitally corrected transposition of the great arteries', 'XPO:0102612', 'abnormal dorsal longitudinal anastomosing vessel - left branch morphology', 0.44, 6.974839882869777, 1.7518360506801718, 'UPHENO:0087186', 'abnormal blood vessel morphology'),
(402961, 'HP:0011540', 'Congenitally corrected transposition of the great arteries', 'XPO:0101708', 'abnormal artery morphology', 0.44, 6.974839882869777, 1.7518360506801718, 'UPHENO:0087186', 'abnormal blood vessel morphology'),
(402962, 'HP:0011540', 'Congenitally corrected transposition of the great arteries', 'XPO:0102565', 'abnormal branchial vein morphology', 0.4339622641509434, 7.803720102857406, 1.8402499951463749, 'HP:0033353', 'Abnormal blood vessel morphology'),
(402963, 'HP:0011540', 'Congenitally corrected transposition of the great arteries', 'XPO:0103215', 'abnormal truncus arteriosus morphology', 0.4583333333333333, 6.974839882869777, 1.7879601821578637, 'UPHENO:0087186', 'abnormal blood vessel morphology'),
(402964, 'HP:0011540', 'Congenitally corrected transposition of the great arteries', 'XPO:0102875', 'abnormal vertebral artery morphology', 0.4230769230769231, 6.974839882869777, 1.717816578275676, 'UPHENO:0087186', 'abnormal blood vessel morphology'),
(402965, 'HP:0011540', 'Congenitally corrected transposition of the great arteries', 'XPO:0140809', 'abnormally necrotic truncus arteriosus', 0.4074074074074074, 6.974839882869777, 1.6857050257271469, 'UPHENO:0087186', 'abnormal blood vessel morphology'),
(402966, 'HP:0011540', 'Congenitally corrected transposition of the great arteries', 'XPO:0101774', 'abnormal paired dorsal aorta morphology', 0.423728813559322, 9.164925931510773, 1.9706453743172878, 'UPHENO:0076765', 'abnormal great vessel of heart morphology'),
(402967, 'HP:0011540', 'Congenitally corrected transposition of the great arteries', 'XPO:0101956', 'abnormal intersomitic vessel morphology', 0.4230769230769231, 6.974839882869777, 1.717816578275676, 'UPHENO:0087186', 'abnormal blood vessel morphology'),
(402968, 'HP:0011540', 'Congenitally corrected transposition of the great arteries', 'XPO:0102424', 'abnormal capillary morphology', 0.45098039215686275, 7.803720102857406, 1.8759863411733644, 'HP:0033353', 'Abnormal blood vessel morphology'),
(402969, 'HP:0011540', 'Congenitally corrected transposition of the great arteries', 'XPO:0103189', 'abnormal Jacobsons vein morphology', 0.4339622641509434, 7.803720102857406, 1.8402499951463749, 'HP:0033353', 'Abnormal blood vessel morphology'),
(402970, 'HP:0011540', 'Congenitally corrected transposition of the great arteries', 'XPO:0102421', 'abnormal occipitovertebral artery morphology', 0.4230769230769231, 6.974839882869777, 1.717816578275676, 'UPHENO:0087186', 'abnormal blood vessel morphology'),
(402971, 'HP:0011540', 'Congenitally corrected transposition of the great arteries', 'XPO:0101712', 'abnormal aorta morphology', 0.43859649122807015, 9.164925931510773, 2.0049200372897116, 'UPHENO:0076765', 'abnormal great vessel of heart morphology'),
(402972, 'HP:0011540', 'Congenitally corrected transposition of the great arteries', 'XPO:0102613', 'abnormal dorsal longitudinal anastomosing vessel morphology', 0.4583333333333333, 6.974839882869777, 1.7879601821578637, 'UPHENO:0087186', 'abnormal blood vessel morphology'),
(402973, 'HP:0011540', 'Congenitally corrected transposition of the great arteries', 'XPO:0141554', 'abnormal blood vessel morphology in the regenerating hindlimb', 0.4230769230769231, 6.974839882869777, 1.717816578275676, 'UPHENO:0087186', 'abnormal blood vessel morphology'),
(402974, 'HP:0011540', 'Congenitally corrected transposition of the great arteries', 'XPO:0102619', 'abnormal larval aorta morphology', 0.4230769230769231, 6.974839882869777, 1.717816578275676, 'UPHENO:0087186', 'abnormal blood vessel morphology'),
(402975, 'HP:0011540', 'Congenitally corrected transposition of the great arteries', 'XPO:0128030', 'decreased size of the blood vessel', 0.41509433962264153, 6.974839882869777, 1.701533589193435, 'UPHENO:0087186', 'abnormal blood vessel morphology'),
(402976, 'HP:0011540', 'Congenitally corrected transposition of the great arteries', 'XPO:0101769', 'abnormal cardinal vein morphology', 0.41818181818181815, 7.803720102857406, 1.806481071363582, 'HP:0033353', 'Abnormal blood vessel morphology'),
(402977, 'HP:0011540', 'Congenitally corrected transposition of the great arteries', 'XPO:0129510', 'increased size of the blood vessel', 0.41509433962264153, 6.974839882869777, 1.701533589193435, 'UPHENO:0087186', 'abnormal blood vessel morphology'),
(402978, 'HP:0011540', 'Congenitally corrected transposition of the great arteries', 'XPO:0140152', 'abnormally necrotic capillary', 0.40350877192982454, 7.803720102857406, 1.7745054283343504, 'HP:0033353', 'Abnormal blood vessel morphology'),
(402979, 'HP:0011540', 'Congenitally corrected transposition of the great arteries', 'XPO:0102683', 'abnormal intersomitic vein morphology', 0.4074074074074074, 6.974839882869777, 1.6857050257271469, 'UPHENO:0087186', 'abnormal blood vessel morphology'),
(402980, 'HP:0011540', 'Congenitally corrected transposition of the great arteries', 'XPO:0101916', 'abnormal tail vasculature morphology', 0.4074074074074074, 6.974839882869777, 1.6857050257271469, 'UPHENO:0087186', 'abnormal blood vessel morphology'),
(402981, 'HP:0011540', 'Congenitally corrected transposition of the great arteries', 'XPO:0139723', 'abnormally necrotic blood vessel', 0.43137254901960786, 6.974839882869777, 1.734576161278933, 'UPHENO:0087186', 'abnormal blood vessel morphology'),
(402982, 'HP:0011540', 'Congenitally corrected transposition of the great arteries', 'XPO:0102154', 'abnormal subinterstitial vein morphology', 0.4339622641509434, 7.803720102857406, 1.8402499951463749, 'HP:0033353', 'Abnormal blood vessel morphology'),
(402983, 'HP:0011540', 'Congenitally corrected transposition of the great arteries', 'XPO:0103063', 'abnormal ischiadic artery morphology', 0.4230769230769231, 6.974839882869777, 1.717816578275676, 'UPHENO:0087186', 'abnormal blood vessel morphology'),
(402984, 'HP:0011540', 'Congenitally corrected transposition of the great arteries', 'XPO:0103217', 'abnormal dorsal longitudinal anastomosing vessel - right branch morphology', 0.44, 6.974839882869777, 1.7518360506801718, 'UPHENO:0087186', 'abnormal blood vessel morphology'),
(402985, 'HP:0011540', 'Congenitally corrected transposition of the great arteries', 'XPO:0101686', 'abnormal blood vessel morphology', 0.4782608695652174, 6.974839882869777, 1.8264153381581798, 'UPHENO:0087186', 'abnormal blood vessel morphology'),
(402986, 'HP:0011540', 'Congenitally corrected transposition of the great arteries', 'XPO:0140595', 'abnormally necrotic dorsal longitudinal anastomosing vessel', 0.4074074074074074, 6.974839882869777, 1.6857050257271469, 'UPHENO:0087186', 'abnormal blood vessel morphology'),
(402987, 'HP:0008116', 'Flexion limitation of toes', 'XPO:0100768', 'abnormal pectoral girdle', 0.4375, 9.463856994035337, 2.0348064858581663, 'UPHENO:0002647', 'abnormal musculature of limb'),
(402988, 'HP:0011125', 'Abnormality of dermal melanosomes', 'XPO:0100006', 'abnormal anatomical structure', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(402989, 'HP:0011125', 'Abnormality of dermal melanosomes', 'XPO:0100337', 'abnormal zygote', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(402990, 'HP:0011125', 'Abnormality of dermal melanosomes', 'XPO:0102945', 'abnormal Eberth-Kastschenko layer morphology', 0.42857142857142855, 7.420886955069779, 1.7833620281931915, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(402991, 'HP:0011125', 'Abnormality of dermal melanosomes', 'XPO:0100544', 'abnormal neuromast support cell', 0.4411764705882353, 6.8660902472206855, 1.740447489012273, 'HP:0000951', 'Abnormality of the skin'),
(402992, 'HP:0011125', 'Abnormality of dermal melanosomes', 'XPO:0100994', 'abnormal granular gland', 0.46875, 6.8660902472206855, 1.7940122082596586, 'HP:0000951', 'Abnormality of the skin'),
(402993, 'HP:0011125', 'Abnormality of dermal melanosomes', 'XPO:0100507', 'abnormal skin', 0.5, 6.8660902472206855, 1.8528478414619864, 'HP:0000951', 'Abnormality of the skin'),
(402994, 'HP:0011125', 'Abnormality of dermal melanosomes', 'XPO:0102626', 'abnormal granular gland morphology', 0.43902439024390244, 7.420886955069779, 1.8049793268950312, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(402995, 'HP:0011125', 'Abnormality of dermal melanosomes', 'XPO:0100172', 'abnormal stem cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(402996, 'HP:0011125', 'Abnormality of dermal melanosomes', 'XPO:0102910', 'abnormal pigment cell morphology', 0.42857142857142855, 7.420886955069779, 1.7833620281931915, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(402997, 'HP:0011125', 'Abnormality of dermal melanosomes', 'XPO:0100026', 'abnormal germ cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(402998, 'HP:0011125', 'Abnormality of dermal melanosomes', 'XPO:0102886', 'abnormal stratum compactum morphology', 0.42857142857142855, 7.420886955069779, 1.7833620281931915, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(402999, 'HP:0011125', 'Abnormality of dermal melanosomes', 'XPO:0102176', 'abnormal neuromast support cell morphology', 0.42857142857142855, 7.420886955069779, 1.7833620281931915, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(403000, 'HP:0011125', 'Abnormality of dermal melanosomes', 'XPO:0100691', 'abnormal keratin accumulating cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(403001, 'HP:0011125', 'Abnormality of dermal melanosomes', 'XPO:0101237', 'abnormal mucus secreting cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(403002, 'HP:0011125', 'Abnormality of dermal melanosomes', 'XPO:0101326', 'abnormal cementoblast', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(403003, 'HP:0011125', 'Abnormality of dermal melanosomes', 'XPO:0100754', 'abnormal electrically active cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(403004, 'HP:0011125', 'Abnormality of dermal melanosomes', 'XPO:0100653', 'abnormal myoblast', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(403005, 'HP:0011125', 'Abnormality of dermal melanosomes', 'XPO:0101467', 'abnormal alkali secreting cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(403006, 'HP:0011125', 'Abnormality of dermal melanosomes', 'XPO:0101254', 'abnormal stratum compactum', 0.4411764705882353, 6.8660902472206855, 1.740447489012273, 'HP:0000951', 'Abnormality of the skin'),
(403007, 'HP:0011125', 'Abnormality of dermal melanosomes', 'XPO:0102727', 'abnormal skin seromucous gland morphology', 0.43902439024390244, 7.420886955069779, 1.8049793268950312, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(403008, 'HP:0011125', 'Abnormality of dermal melanosomes', 'XPO:0101313', 'abnormal Eberth-Kastschenko layer', 0.4411764705882353, 6.8660902472206855, 1.740447489012273, 'HP:0000951', 'Abnormality of the skin'),
(403009, 'HP:0011125', 'Abnormality of dermal melanosomes', 'XPO:0100929', 'abnormal dermis', 0.46875, 6.8660902472206855, 1.7940122082596586, 'HP:0000951', 'Abnormality of the skin'),
(403010, 'HP:0011125', 'Abnormality of dermal melanosomes', 'XPO:0100481', 'abnormal anatomical line', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(403011, 'HP:0011125', 'Abnormality of dermal melanosomes', 'XPO:0101529', 'abnormal skin mucous gland', 0.4411764705882353, 6.8660902472206855, 1.740447489012273, 'HP:0000951', 'Abnormality of the skin'),
(403012, 'HP:0011125', 'Abnormality of dermal melanosomes', 'XPO:0100549', 'abnormal mitotic cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(403013, 'HP:0011125', 'Abnormality of dermal melanosomes', 'XPO:0101448', 'abnormal myelin accumulating cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(403014, 'HP:0011125', 'Abnormality of dermal melanosomes', 'XPO:0100704', 'abnormal Merkel cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(403015, 'HP:0011125', 'Abnormality of dermal melanosomes', 'XPO:0100983', 'abnormal skin gland', 0.4838709677419355, 6.8660902472206855, 1.8227182263109507, 'HP:0000951', 'Abnormality of the skin'),
(403016, 'HP:0011125', 'Abnormality of dermal melanosomes', 'XPO:0101095', 'abnormal skin seromucous gland', 0.46875, 6.8660902472206855, 1.7940122082596586, 'HP:0000951', 'Abnormality of the skin'),
(403017, 'HP:0011125', 'Abnormality of dermal melanosomes', 'XPO:0100533', 'abnormal melanoblast', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(403018, 'HP:0011125', 'Abnormality of dermal melanosomes', 'XPO:0100108', 'abnormal cell part', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(403019, 'HP:0011125', 'Abnormality of dermal melanosomes', 'XPO:0103223', 'abnormal xanthophore morphology', 0.4090909090909091, 7.420886955069779, 1.7423597190908553, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(403020, 'HP:0011125', 'Abnormality of dermal melanosomes', 'XPO:0100852', 'abnormal interdigital region', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(403021, 'HP:0011125', 'Abnormality of dermal melanosomes', 'XPO:0101333', 'abnormal barrier epithelial cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(403022, 'HP:0011125', 'Abnormality of dermal melanosomes', 'XPO:0101373', 'abnormal oxygen accumulating cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(403023, 'HP:0011125', 'Abnormality of dermal melanosomes', 'XPO:0101208', 'abnormal stratum spongiosum', 0.4411764705882353, 6.8660902472206855, 1.740447489012273, 'HP:0000951', 'Abnormality of the skin'),
(403024, 'HP:0011125', 'Abnormality of dermal melanosomes', 'XPO:0100344', 'abnormal portion of organism substance', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(403025, 'HP:0011125', 'Abnormality of dermal melanosomes', 'XPO:0102840', 'abnormal stratum spongiosum morphology', 0.42857142857142855, 7.420886955069779, 1.7833620281931915, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(403026, 'HP:0011125', 'Abnormality of dermal melanosomes', 'XPO:0102615', 'abnormal skin gland morphology', 0.46153846153846156, 7.420886955069779, 1.8506822386605823, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(403027, 'HP:0011125', 'Abnormality of dermal melanosomes', 'XPO:0103019', 'abnormal melanophore morphology', 0.4090909090909091, 7.420886955069779, 1.7423597190908553, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(403028, 'HP:0011125', 'Abnormality of dermal melanosomes', 'XPO:0100004', 'abnormal cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(403029, 'HP:0011125', 'Abnormality of dermal melanosomes', 'XPO:0100285', 'abnormal progenitor cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(403030, 'HP:0011125', 'Abnormality of dermal melanosomes', 'XPO:0102954', 'abnormal iridophore morphology', 0.4090909090909091, 7.420886955069779, 1.7423597190908553, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(403031, 'HP:0011125', 'Abnormality of dermal melanosomes', 'XPO:0103147', 'abnormal neuromast mantle cell morphology', 0.42857142857142855, 7.420886955069779, 1.7833620281931915, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(403032, 'HP:0011125', 'Abnormality of dermal melanosomes', 'XPO:0100289', 'abnormal chondroblast', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(403033, 'HP:0011125', 'Abnormality of dermal melanosomes', 'XPO:0100715', 'abnormal ciliated cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(403034, 'HP:0011125', 'Abnormality of dermal melanosomes', 'XPO:0100081', 'abnormal anatomical entity in vitro', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(403035, 'HP:0011125', 'Abnormality of dermal melanosomes', 'XPO:0101004', 'abnormal acid secreting cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(403036, 'HP:0011125', 'Abnormality of dermal melanosomes', 'XPO:0101014', 'abnormal goblet cell', 0.40540540540540543, 6.8660902472206855, 1.6683974647021622, 'HP:0000951', 'Abnormality of the skin'),
(403037, 'HP:0011125', 'Abnormality of dermal melanosomes', 'XPO:0101515', 'abnormal neuromast mantle cell', 0.4411764705882353, 6.8660902472206855, 1.740447489012273, 'HP:0000951', 'Abnormality of the skin'),
(403038, 'HP:0011125', 'Abnormality of dermal melanosomes', 'XPO:0100802', 'abnormal exocrine cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(403039, 'HP:0011125', 'Abnormality of dermal melanosomes', 'XPO:0101591', 'abnormal xanthophore', 0.42857142857142855, 6.8660902472206855, 1.7154037734456928, 'HP:0000951', 'Abnormality of the skin'),
(403040, 'HP:0011125', 'Abnormality of dermal melanosomes', 'XPO:0101132', 'abnormal apoptotic cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(403041, 'HP:0011125', 'Abnormality of dermal melanosomes', 'XPO:0101387', 'abnormal melanophore', 0.42857142857142855, 6.8660902472206855, 1.7154037734456928, 'HP:0000951', 'Abnormality of the skin'),
(403042, 'HP:0011125', 'Abnormality of dermal melanosomes', 'XPO:0101435', 'abnormal paracrine cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(403043, 'HP:0011125', 'Abnormality of dermal melanosomes', 'XPO:0102139', 'abnormal skin morphology', 0.46153846153846156, 7.420886955069779, 1.8506822386605823, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(403044, 'HP:0011125', 'Abnormality of dermal melanosomes', 'XPO:0101535', 'abnormal absorptive cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(403045, 'HP:0011125', 'Abnormality of dermal melanosomes', 'XPO:0100791', 'abnormal multiciliated cell precursor', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(403046, 'HP:0011125', 'Abnormality of dermal melanosomes', 'XPO:0101241', 'abnormal nucleate erythrocyte', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(403047, 'HP:0011125', 'Abnormality of dermal melanosomes', 'XPO:0100477', 'abnormal pericyte', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(403048, 'HP:0011125', 'Abnormality of dermal melanosomes', 'XPO:0101322', 'abnormal iridophore', 0.42857142857142855, 6.8660902472206855, 1.7154037734456928, 'HP:0000951', 'Abnormality of the skin'),
(403049, 'HP:0011125', 'Abnormality of dermal melanosomes', 'XPO:0100638', 'abnormal polar body', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(403050, 'HP:0011125', 'Abnormality of dermal melanosomes', 'XPO:0101297', 'abnormal barrier cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(403051, 'HP:0011125', 'Abnormality of dermal melanosomes', 'XPO:0102561', 'abnormal dermis morphology', 0.45, 7.420886955069779, 1.8274022900777487, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(403052, 'HP:0011125', 'Abnormality of dermal melanosomes', 'XPO:0101278', 'abnormal pigment cell', 0.4411764705882353, 6.8660902472206855, 1.740447489012273, 'HP:0000951', 'Abnormality of the skin'),
(403053, 'HP:0032523', 'Tendon thickening', 'XPO:0102693', 'abnormal plasma membrane morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(403054, 'HP:0032523', 'Tendon thickening', 'XPO:0130293', 'increased size of the intersomitic tendon', 0.45454545454545453, 10.802658907487096, 2.21591956158233, 'UPHENO:0021425', 'abnormal tendon morphology'),
(403055, 'HP:0032523', 'Tendon thickening', 'XPO:0142064', 'abnormal desmosome morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(403056, 'HP:0032523', 'Tendon thickening', 'XPO:0140350', 'abnormally necrotic notochordal sheath', 0.45454545454545453, 4.638757693672553, 1.452076521536181, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(403057, 'HP:0032523', 'Tendon thickening', 'XPO:0102010', 'abnormal perichondrium morphology', 0.5789473684210527, 6.985637650836012, 2.0110486156964313, 'UPHENO:0002712', 'abnormal connective tissue'),
(403058, 'HP:0032523', 'Tendon thickening', 'XPO:0130188', 'increased size of the flexural organ', 0.43478260869565216, 4.638757693672553, 1.4201588541997616, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(403059, 'HP:0032523', 'Tendon thickening', 'XPO:0101174', 'abnormal articular system', 0.4117647058823529, 4.3395673355180735, 1.3367425584480601, 'UPHENO:0002964', 'abnormal skeletal system'),
(403060, 'HP:0032523', 'Tendon thickening', 'XPO:0102542', 'abnormal vacuolated notochordal tissue morphology', 0.5365853658536586, 6.985637650836012, 1.9360761696263227, 'UPHENO:0002712', 'abnormal connective tissue'),
(403061, 'HP:0032523', 'Tendon thickening', 'XPO:0102514', 'abnormal perichondrial cell morphology', 0.5238095238095238, 6.985637650836012, 1.91288879221723, 'UPHENO:0002712', 'abnormal connective tissue'),
(403062, 'HP:0032523', 'Tendon thickening', 'XPO:0101740', 'abnormal cell part morphology', 0.42857142857142855, 2.786899518863159, 1.092879457252359, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(403063, 'HP:0032523', 'Tendon thickening', 'XPO:0140182', 'abnormally necrotic dense regular connective tissue', 0.4090909090909091, 6.985637650836012, 1.6904913064432443, 'UPHENO:0002712', 'abnormal connective tissue'),
(403064, 'HP:0032523', 'Tendon thickening', 'XPO:0102049', 'abnormal dense regular connective tissue morphology', 0.47368421052631576, 6.985637650836012, 1.8190619163896438, 'UPHENO:0002712', 'abnormal connective tissue'),
(403065, 'HP:0032523', 'Tendon thickening', 'XPO:0100377', 'abnormal connective tissue', 0.4375, 6.985637650836012, 1.748203784528782, 'UPHENO:0002712', 'abnormal connective tissue'),
(403066, 'HP:0032523', 'Tendon thickening', 'XPO:0140559', 'abnormally necrotic articular system', 0.46511627906976744, 4.638757693672553, 1.4688640910537754, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(403067, 'HP:0032523', 'Tendon thickening', 'XPO:0139718', 'abnormally necrotic anatomical structure', 0.41935483870967744, 2.786899518863159, 1.0810641970914296, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(403068, 'HP:0032523', 'Tendon thickening', 'XPO:0103201', 'abnormal activin-induced ectoderm morphology', 0.41935483870967744, 2.786899518863159, 1.0810641970914296, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(403069, 'HP:0032523', 'Tendon thickening', 'XPO:0101755', 'abnormal pelvic girdle morphology', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(403070, 'HP:0032523', 'Tendon thickening', 'XPO:0107399', 'abnormal filopodium morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(403071, 'HP:0032523', 'Tendon thickening', 'XPO:0107285', 'abnormal flexural organ', 0.4117647058823529, 4.3395673355180735, 1.3367425584480601, 'UPHENO:0002964', 'abnormal skeletal system'),
(403072, 'HP:0032523', 'Tendon thickening', 'XPO:0102728', 'abnormal tendon morphology', 0.625, 10.802658907487096, 2.5983960085366964, 'UPHENO:0021425', 'abnormal tendon morphology'),
(403073, 'HP:0032523', 'Tendon thickening', 'XPO:0130294', 'increased size of the tendon', 0.5102040816326531, 10.802658907487096, 2.3476713285903656, 'UPHENO:0021425', 'abnormal tendon morphology'),
(403074, 'HP:0032523', 'Tendon thickening', 'XPO:0101981', 'abnormal ossicle morphology', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(403075, 'HP:0032523', 'Tendon thickening', 'XPO:0130762', 'increased size of the perichondrial cell', 0.4074074074074074, 6.985637650836012, 1.6870093433098323, 'UPHENO:0002712', 'abnormal connective tissue'),
(403076, 'HP:0032523', 'Tendon thickening', 'XPO:0141277', 'abnormal actin cytoskeleton morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(403077, 'HP:0032523', 'Tendon thickening', 'XPO:0141719', 'abnormal anterior notochord morphology', 0.5128205128205128, 4.638757693672553, 1.5423521320759594, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(403078, 'HP:0032523', 'Tendon thickening', 'XPO:0101680', 'abnormal skeletal element morphology', 0.43478260869565216, 4.638757693672553, 1.4201588541997616, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(403079, 'HP:0032523', 'Tendon thickening', 'XPO:0102130', 'abnormal endoskeleton morphology', 0.47619047619047616, 4.638757693672553, 1.4862477031377266, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(403080, 'HP:0032523', 'Tendon thickening', 'XPO:0101871', 'abnormal acellular anatomical structure morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(403081, 'HP:0032523', 'Tendon thickening', 'XPO:0101998', 'abnormal non-mineralized chondroid tissue morphology', 0.44, 6.985637650836012, 1.753191537273622, 'UPHENO:0002712', 'abnormal connective tissue'),
(403082, 'HP:0032523', 'Tendon thickening', 'XPO:0102526', 'abnormal nucleus morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(403083, 'HP:0032523', 'Tendon thickening', 'XPO:0102601', 'abnormal disaggregated/reaggregated ectoderm treated with activin morphology', 0.41935483870967744, 2.786899518863159, 1.0810641970914296, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(403084, 'HP:0032523', 'Tendon thickening', 'XPO:0100882', 'abnormal perichondrial cell', 0.43243243243243246, 6.985637650836012, 1.7380495624240986, 'UPHENO:0002712', 'abnormal connective tissue'),
(403085, 'HP:0032523', 'Tendon thickening', 'XPO:0128815', 'decreased size of the intersomitic tendon', 0.45454545454545453, 10.802658907487096, 2.21591956158233, 'UPHENO:0021425', 'abnormal tendon morphology'),
(403086, 'HP:0032523', 'Tendon thickening', 'XPO:0100584', 'abnormal vertebral column', 0.45454545454545453, 4.638757693672553, 1.452076521536181, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(403087, 'HP:0032523', 'Tendon thickening', 'XPO:0141296', 'abnormal adherens junction morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(403088, 'HP:0032523', 'Tendon thickening', 'XPO:0102714', 'abnormal mineralized hyaline cartilage tissue morphology', 0.4230769230769231, 6.985637650836012, 1.719145742235371, 'UPHENO:0002712', 'abnormal connective tissue'),
(403089, 'HP:0032523', 'Tendon thickening', 'XPO:0140722', 'abnormally necrotic intersomitic tendon', 0.4716981132075472, 10.802658907487096, 2.257342203629385, 'UPHENO:0021425', 'abnormal tendon morphology'),
(403090, 'HP:0032523', 'Tendon thickening', 'XPO:0101976', 'abnormal portion of organism substance morphology', 0.4482758620689655, 2.786899518863159, 1.1177207989108764, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(403091, 'HP:0032523', 'Tendon thickening', 'XPO:0102588', 'abnormal centrosome morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(403092, 'HP:0032523', 'Tendon thickening', 'XPO:0141699', 'abnormally necrotic anterior notochord', 0.45454545454545453, 4.638757693672553, 1.452076521536181, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(403093, 'HP:0032523', 'Tendon thickening', 'XPO:0102539', 'abnormal cytoplasm morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(403094, 'HP:0032523', 'Tendon thickening', 'XPO:0100640', 'abnormal notochordal sheath', 0.4117647058823529, 4.3395673355180735, 1.3367425584480601, 'UPHENO:0002964', 'abnormal skeletal system'),
(403095, 'HP:0032523', 'Tendon thickening', 'XPO:0140432', 'abnormally necrotic skeleton', 0.45454545454545453, 4.638757693672553, 1.452076521536181, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(403096, 'HP:0032523', 'Tendon thickening', 'XPO:0128158', 'decreased size of the skeletal subdivision', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(403097, 'HP:0032523', 'Tendon thickening', 'XPO:0102353', 'abnormal centromere morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(403098, 'HP:0032523', 'Tendon thickening', 'XPO:0100910', 'abnormal vacuolated notochordal tissue', 0.45714285714285713, 6.985637650836012, 1.787018286047429, 'UPHENO:0002712', 'abnormal connective tissue'),
(403099, 'HP:0032523', 'Tendon thickening', 'XPO:0128132', 'decreased size of the perichondrium', 0.4782608695652174, 6.985637650836012, 1.827828530622157, 'UPHENO:0002712', 'abnormal connective tissue'),
(403100, 'HP:0032523', 'Tendon thickening', 'XPO:0101764', 'abnormal cranium morphology', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(403101, 'HP:0032523', 'Tendon thickening', 'XPO:0100465', 'abnormal skeletal system', 0.42424242424242425, 4.3395673355180735, 1.3568450783281876, 'UPHENO:0002964', 'abnormal skeletal system'),
(403102, 'HP:0032523', 'Tendon thickening', 'XPO:0102054', 'abnormal notochord morphology', 0.5128205128205128, 4.638757693672553, 1.5423521320759594, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(403103, 'HP:0032523', 'Tendon thickening', 'XPO:0102761', 'abnormal cartilaginous condensation morphology', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(403104, 'HP:0032523', 'Tendon thickening', 'XPO:0101890', 'abnormal organ part morphology', 0.41935483870967744, 2.786899518863159, 1.0810641970914296, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(403105, 'HP:0032523', 'Tendon thickening', 'XPO:0141708', 'decreased size of the posterior notochord', 0.43478260869565216, 4.638757693672553, 1.4201588541997616, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(403106, 'HP:0032523', 'Tendon thickening', 'XPO:0102489', 'abnormal periosteum (sensu fibrous layer) morphology', 0.4230769230769231, 6.985637650836012, 1.719145742235371, 'UPHENO:0002712', 'abnormal connective tissue'),
(403107, 'HP:0032523', 'Tendon thickening', 'XPO:0140123', 'abnormally necrotic perichondrial cell', 0.4782608695652174, 6.985637650836012, 1.827828530622157, 'UPHENO:0002712', 'abnormal connective tissue'),
(403108, 'HP:0032523', 'Tendon thickening', 'XPO:0102320', 'abnormal adipose tissue morphology', 0.45, 6.985637650836012, 1.7730022399523937, 'UPHENO:0002712', 'abnormal connective tissue'),
(403109, 'HP:0032523', 'Tendon thickening', 'XPO:0101636', 'abnormal cell morphology', 0.4166666666666667, 2.786899518863159, 1.0775936770692605, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(403110, 'HP:0032523', 'Tendon thickening', 'XPO:0102272', 'abnormal notochordal sheath morphology', 0.5128205128205128, 4.638757693672553, 1.5423521320759594, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(403111, 'HP:0032523', 'Tendon thickening', 'XPO:0102245', 'abnormal periosteum (sensu osteogenic layer) morphology', 0.4230769230769231, 6.985637650836012, 1.719145742235371, 'UPHENO:0002712', 'abnormal connective tissue'),
(403112, 'HP:0032523', 'Tendon thickening', 'XPO:0100378', 'abnormal perichondrium', 0.48484848484848486, 6.985637650836012, 1.8403738290652716, 'UPHENO:0002712', 'abnormal connective tissue'),
(403113, 'HP:0032523', 'Tendon thickening', 'XPO:0129584', 'increased size of the connective tissue', 0.4186046511627907, 6.985637650836012, 1.710035207818209, 'UPHENO:0002712', 'abnormal connective tissue'),
(403114, 'HP:0032523', 'Tendon thickening', 'XPO:0102055', 'abnormal process morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(403115, 'HP:0032523', 'Tendon thickening', 'XPO:0140683', 'abnormally necrotic flexural organ', 0.45454545454545453, 4.638757693672553, 1.452076521536181, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(403116, 'HP:0032523', 'Tendon thickening', 'XPO:0101854', 'abnormal bone element morphology', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(403117, 'HP:0032523', 'Tendon thickening', 'XPO:0102011', 'abnormal periosteum morphology', 0.43137254901960786, 6.985637650836012, 1.7359182929989752, 'UPHENO:0002712', 'abnormal connective tissue'),
(403118, 'HP:0032523', 'Tendon thickening', 'XPO:0141713', 'increased size of the posterior notochord', 0.43478260869565216, 4.638757693672553, 1.4201588541997616, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(403119, 'HP:0032523', 'Tendon thickening', 'XPO:0100417', 'abnormal dense regular connective tissue', 0.42424242424242425, 6.985637650836012, 1.721512082986879, 'UPHENO:0002712', 'abnormal connective tissue'),
(403120, 'HP:0032523', 'Tendon thickening', 'XPO:0100585', 'abnormal elastica externa', 0.4375, 4.3395673355180735, 1.3778826906849353, 'UPHENO:0002964', 'abnormal skeletal system'),
(403121, 'HP:0032523', 'Tendon thickening', 'XPO:0102062', 'abnormal odontoid tissue morphology', 0.4074074074074074, 6.985637650836012, 1.6870093433098323, 'UPHENO:0002712', 'abnormal connective tissue'),
(403122, 'HP:0032523', 'Tendon thickening', 'XPO:0128709', 'decreased size of the flexural organ', 0.43478260869565216, 4.638757693672553, 1.4201588541997616, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(403123, 'HP:0032523', 'Tendon thickening', 'XPO:0107372', 'abnormal flexural organ morphology', 0.5128205128205128, 4.638757693672553, 1.5423521320759594, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(403124, 'HP:0032523', 'Tendon thickening', 'XPO:0102360', 'abnormal cell condensation morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(403125, 'HP:0032523', 'Tendon thickening', 'XPO:0139806', 'abnormally necrotic vacuolated notochordal tissue', 0.46808510638297873, 6.985637650836012, 1.808279000305129, 'UPHENO:0002712', 'abnormal connective tissue'),
(403126, 'HP:0032523', 'Tendon thickening', 'XPO:0129832', 'increased size of the skeletal system', 0.45454545454545453, 4.638757693672553, 1.452076521536181, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(403127, 'HP:0032523', 'Tendon thickening', 'XPO:0141718', 'abnormal posterior notochord', 0.4117647058823529, 4.3395673355180735, 1.3367425584480601, 'UPHENO:0002964', 'abnormal skeletal system'),
(403128, 'HP:0032523', 'Tendon thickening', 'XPO:0141316', 'abnormal anatomical region morphology', 0.41935483870967744, 2.786899518863159, 1.0810641970914296, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(403129, 'HP:0032523', 'Tendon thickening', 'XPO:0130908', 'increased size of the notochordal sheath', 0.43478260869565216, 4.638757693672553, 1.4201588541997616, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(403130, 'HP:0032523', 'Tendon thickening', 'XPO:0102217', 'abnormal elastica externa morphology', 0.5405405405405406, 4.638757693672553, 1.5834887404633964, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(403131, 'HP:0032523', 'Tendon thickening', 'XPO:0129612', 'increased size of the perichondrium', 0.4782608695652174, 6.985637650836012, 1.827828530622157, 'UPHENO:0002712', 'abnormal connective tissue'),
(403132, 'HP:0032523', 'Tendon thickening', 'XPO:0100422', 'abnormal notochord', 0.42424242424242425, 4.3395673355180735, 1.3568450783281876, 'UPHENO:0002964', 'abnormal skeletal system'),
(403133, 'HP:0032523', 'Tendon thickening', 'XPO:0129434', 'decreased size of the notochordal sheath', 0.43478260869565216, 4.638757693672553, 1.4201588541997616, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(403134, 'HP:0032523', 'Tendon thickening', 'XPO:0140660', 'abnormally necrotic tendon', 0.5319148936170213, 10.802658907487096, 2.3971014086927918, 'UPHENO:0021425', 'abnormal tendon morphology'),
(403135, 'HP:0032523', 'Tendon thickening', 'XPO:0107345', 'abnormal anatomical axis morphology', 0.41935483870967744, 2.786899518863159, 1.0810641970914296, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(403136, 'HP:0032523', 'Tendon thickening', 'XPO:0103179', 'abnormal lampbrush chromosome morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(403137, 'HP:0032523', 'Tendon thickening', 'XPO:0103737', 'increased size of the notochord', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(403138, 'HP:0032523', 'Tendon thickening', 'XPO:0102093', 'abnormal craniofacial skeleton morphology', 0.43478260869565216, 4.638757693672553, 1.4201588541997616, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(403139, 'HP:0032523', 'Tendon thickening', 'XPO:0141703', 'abnormally necrotic posterior notochord', 0.45454545454545453, 4.638757693672553, 1.452076521536181, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(403140, 'HP:0032523', 'Tendon thickening', 'XPO:0139771', 'abnormally necrotic skeletal subdivision', 0.4444444444444444, 4.638757693672553, 1.4358516936218344, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(403141, 'HP:0032523', 'Tendon thickening', 'XPO:0103145', 'abnormal basal body morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(403142, 'HP:0032523', 'Tendon thickening', 'XPO:0102806', 'abnormal articular system morphology', 0.5263157894736842, 4.638757693672553, 1.5625144536043167, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(403143, 'HP:0032523', 'Tendon thickening', 'XPO:0141714', 'abnormal anterior notochord', 0.4117647058823529, 4.3395673355180735, 1.3367425584480601, 'UPHENO:0002964', 'abnormal skeletal system'),
(403144, 'HP:0032523', 'Tendon thickening', 'XPO:0101348', 'abnormal perichordal tissue', 0.45714285714285713, 6.985637650836012, 1.787018286047429, 'UPHENO:0002712', 'abnormal connective tissue'),
(403145, 'HP:0032523', 'Tendon thickening', 'XPO:0139989', 'abnormally necrotic skeletal tissue', 0.4074074074074074, 6.985637650836012, 1.6870093433098323, 'UPHENO:0002712', 'abnormal connective tissue'),
(403146, 'HP:0032523', 'Tendon thickening', 'XPO:0129936', 'increased size of the vacuolated notochordal tissue', 0.4489795918367347, 6.985637650836012, 1.7709908924643512, 'UPHENO:0002712', 'abnormal connective tissue'),
(403147, 'HP:0032523', 'Tendon thickening', 'XPO:0103116', 'abnormal bone marrow morphology', 0.43478260869565216, 4.638757693672553, 1.4201588541997616, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(403148, 'HP:0032523', 'Tendon thickening', 'XPO:0129664', 'increased size of the skeleton', 0.43478260869565216, 4.638757693672553, 1.4201588541997616, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(403149, 'HP:0032523', 'Tendon thickening', 'XPO:0139917', 'abnormally necrotic notochord', 0.4444444444444444, 4.638757693672553, 1.4358516936218344, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(403150, 'HP:0032523', 'Tendon thickening', 'XPO:0128306', 'decreased size of the articular system', 0.4444444444444444, 4.638757693672553, 1.4358516936218344, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(403151, 'HP:0032523', 'Tendon thickening', 'XPO:0140812', 'abnormally necrotic endoskeleton', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(403152, 'HP:0032523', 'Tendon thickening', 'XPO:0101860', 'abnormal skeletal subdivision morphology', 0.5, 4.638757693672553, 1.5229507040072823, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(403153, 'HP:0032523', 'Tendon thickening', 'XPO:0140043', 'abnormally necrotic perichondrium', 0.5, 6.985637650836012, 1.8689084582766504, 'UPHENO:0002712', 'abnormal connective tissue'),
(403154, 'HP:0032523', 'Tendon thickening', 'XPO:0128184', 'decreased size of the skeleton', 0.43478260869565216, 4.638757693672553, 1.4201588541997616, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(403155, 'HP:0032523', 'Tendon thickening', 'XPO:0101957', 'abnormal axial skeleton morphology', 0.46511627906976744, 4.638757693672553, 1.4688640910537754, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(403156, 'HP:0032523', 'Tendon thickening', 'XPO:0102178', 'abnormal whole organism morphology', 0.41935483870967744, 2.786899518863159, 1.0810641970914296, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(403157, 'HP:0032523', 'Tendon thickening', 'XPO:0101642', 'abnormal multicellular anatomical structure morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(403158, 'HP:0032523', 'Tendon thickening', 'XPO:0100416', 'abnormal ligament', 0.4117647058823529, 6.985637650836012, 1.6960067902862834, 'UPHENO:0002712', 'abnormal connective tissue'),
(403159, 'HP:0032523', 'Tendon thickening', 'XPO:0102356', 'abnormal kinetochore morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(403160, 'HP:0032523', 'Tendon thickening', 'XPO:0101096', 'abnormal tendon', 0.4117647058823529, 6.985637650836012, 1.6960067902862834, 'UPHENO:0002712', 'abnormal connective tissue'),
(403161, 'HP:0032523', 'Tendon thickening', 'XPO:0100688', 'abnormal adipose tissue', 0.42424242424242425, 6.985637650836012, 1.721512082986879, 'UPHENO:0002712', 'abnormal connective tissue'),
(403162, 'HP:0032523', 'Tendon thickening', 'XPO:0139998', 'abnormally necrotic axial skeleton', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(403163, 'HP:0032523', 'Tendon thickening', 'XPO:0141723', 'abnormal posterior notochord morphology', 0.5128205128205128, 4.638757693672553, 1.5423521320759594, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(403164, 'HP:0032523', 'Tendon thickening', 'XPO:0102164', 'abnormal mandibular mesenchyme morphology', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(403165, 'HP:0032523', 'Tendon thickening', 'XPO:0102703', 'abnormal endoplasmic reticulum morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(403166, 'HP:0032523', 'Tendon thickening', 'XPO:0102605', 'abnormal dermal skeleton morphology', 0.47619047619047616, 4.638757693672553, 1.4862477031377266, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(403167, 'HP:0032523', 'Tendon thickening', 'XPO:0102097', 'abnormal skeletal system morphology', 0.5405405405405406, 4.638757693672553, 1.5834887404633964, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(403168, 'HP:0032523', 'Tendon thickening', 'XPO:0102151', 'abnormal mineralized tissue morphology', 0.44, 6.985637650836012, 1.753191537273622, 'UPHENO:0002712', 'abnormal connective tissue'),
(403169, 'HP:0032523', 'Tendon thickening', 'XPO:0129286', 'decreased size of the perichondrial cell', 0.4074074074074074, 6.985637650836012, 1.6870093433098323, 'UPHENO:0002712', 'abnormal connective tissue'),
(403170, 'HP:0032523', 'Tendon thickening', 'XPO:0141709', 'increased size of the anterior notochord', 0.43478260869565216, 4.638757693672553, 1.4201588541997616, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(403171, 'HP:0032523', 'Tendon thickening', 'XPO:0128104', 'decreased size of the connective tissue', 0.4186046511627907, 6.985637650836012, 1.710035207818209, 'UPHENO:0002712', 'abnormal connective tissue'),
(403172, 'HP:0032523', 'Tendon thickening', 'XPO:0115491', 'abnormally increased distribution of connective tissue', 0.4864864864864865, 6.985637650836012, 1.8434799474425876, 'UPHENO:0002712', 'abnormal connective tissue'),
(403173, 'HP:0032523', 'Tendon thickening', 'XPO:0128816', 'decreased size of the tendon', 0.5102040816326531, 10.802658907487096, 2.3476713285903656, 'UPHENO:0021425', 'abnormal tendon morphology'),
(403174, 'HP:0032523', 'Tendon thickening', 'XPO:0102144', 'abnormal cranial skeleton morphology', 0.45454545454545453, 4.638757693672553, 1.452076521536181, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(403175, 'HP:0032523', 'Tendon thickening', 'XPO:0128890', 'decreased size of the elastica externa', 0.45454545454545453, 4.638757693672553, 1.452076521536181, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(403176, 'HP:0032523', 'Tendon thickening', 'XPO:0102773', 'abnormal Keller explant morphology', 0.41935483870967744, 2.786899518863159, 1.0810641970914296, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(403177, 'HP:0032523', 'Tendon thickening', 'XPO:0141704', 'decreased size of the anterior notochord', 0.43478260869565216, 4.638757693672553, 1.4201588541997616, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(403178, 'HP:0032523', 'Tendon thickening', 'XPO:0102980', 'abnormal perichordal tissue morphology', 0.5365853658536586, 6.985637650836012, 1.9360761696263227, 'UPHENO:0002712', 'abnormal connective tissue'),
(403179, 'HP:0032523', 'Tendon thickening', 'XPO:0115510', 'abnormal degeneration of whole organism', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(403180, 'HP:0032523', 'Tendon thickening', 'XPO:0129786', 'increased size of the articular system', 0.4444444444444444, 4.638757693672553, 1.4358516936218344, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(403181, 'HP:0032523', 'Tendon thickening', 'XPO:0103234', 'abnormal intersomitic tendon morphology', 0.5555555555555556, 10.802658907487096, 2.4497912504591417, 'UPHENO:0021425', 'abnormal tendon morphology'),
(403182, 'HP:0032523', 'Tendon thickening', 'XPO:0101694', 'abnormal anatomical space morphology', 0.41935483870967744, 2.786899518863159, 1.0810641970914296, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(403183, 'HP:0032523', 'Tendon thickening', 'XPO:0139793', 'abnormally necrotic connective tissue', 0.43902439024390244, 6.985637650836012, 1.7512467873269968, 'UPHENO:0002712', 'abnormal connective tissue'),
(403184, 'HP:0032523', 'Tendon thickening', 'XPO:0101716', 'abnormal anatomical group morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(403185, 'HP:0032523', 'Tendon thickening', 'XPO:0103218', 'abnormal joint morphology', 0.4444444444444444, 4.638757693672553, 1.4358516936218344, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(403186, 'HP:0032523', 'Tendon thickening', 'XPO:0102794', 'abnormal stromal cell morphology', 0.43902439024390244, 6.985637650836012, 1.7512467873269968, 'UPHENO:0002712', 'abnormal connective tissue'),
(403187, 'HP:0032523', 'Tendon thickening', 'XPO:0139774', 'abnormally necrotic elastica externa', 0.47619047619047616, 4.638757693672553, 1.4862477031377266, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(403188, 'HP:0032523', 'Tendon thickening', 'XPO:0128103', 'decreased size of the perichordal tissue', 0.4489795918367347, 6.985637650836012, 1.7709908924643512, 'UPHENO:0002712', 'abnormal connective tissue'),
(403189, 'HP:0032523', 'Tendon thickening', 'XPO:0130368', 'increased size of the elastica externa', 0.45454545454545453, 4.638757693672553, 1.452076521536181, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(403190, 'HP:0032523', 'Tendon thickening', 'XPO:0139792', 'abnormally necrotic perichordal tissue', 0.46808510638297873, 6.985637650836012, 1.808279000305129, 'UPHENO:0002712', 'abnormal connective tissue'),
(403191, 'HP:0032523', 'Tendon thickening', 'XPO:0102742', 'abnormal cell-free extract morphology', 0.41935483870967744, 2.786899518863159, 1.0810641970914296, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(403192, 'HP:0032523', 'Tendon thickening', 'XPO:0141653', 'neoplastic skeletal element', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(403193, 'HP:0032523', 'Tendon thickening', 'XPO:0102896', 'abnormal mitotic spindle morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(403194, 'HP:0032523', 'Tendon thickening', 'XPO:0140108', 'abnormally necrotic dermal skeleton', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(403195, 'HP:0032523', 'Tendon thickening', 'XPO:0129583', 'increased size of the perichordal tissue', 0.4489795918367347, 6.985637650836012, 1.7709908924643512, 'UPHENO:0002712', 'abnormal connective tissue'),
(403196, 'HP:0032523', 'Tendon thickening', 'XPO:0102009', 'abnormal connective tissue morphology', 0.5, 6.985637650836012, 1.8689084582766504, 'UPHENO:0002712', 'abnormal connective tissue'),
(403197, 'HP:0032523', 'Tendon thickening', 'XPO:0101638', 'abnormal anatomical structure morphology', 0.4482758620689655, 2.786899518863159, 1.1177207989108764, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(403198, 'HP:0032523', 'Tendon thickening', 'XPO:0140019', 'abnormally necrotic skeletal system', 0.47619047619047616, 4.638757693672553, 1.4862477031377266, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(403199, 'HP:0032523', 'Tendon thickening', 'XPO:0101982', 'abnormal appendicular skeleton morphology', 0.45454545454545453, 4.638757693672553, 1.452076521536181, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(403200, 'HP:0032523', 'Tendon thickening', 'XPO:0103355', 'decreased size of the notochord', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(403201, 'HP:0032523', 'Tendon thickening', 'XPO:0102461', 'abnormal postcranial axial skeleton morphology', 0.43478260869565216, 4.638757693672553, 1.4201588541997616, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(403202, 'HP:0032523', 'Tendon thickening', 'XPO:0101713', 'abnormal anatomical entity in vitro morphology', 0.4482758620689655, 2.786899518863159, 1.1177207989108764, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(403203, 'HP:0032523', 'Tendon thickening', 'XPO:0102106', 'abnormal cartilage tissue morphology', 0.41509433962264153, 6.985637650836012, 1.7028501541582675, 'UPHENO:0002712', 'abnormal connective tissue'),
(403204, 'HP:0032523', 'Tendon thickening', 'XPO:0128352', 'decreased size of the skeletal system', 0.45454545454545453, 4.638757693672553, 1.452076521536181, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(403205, 'HP:0032523', 'Tendon thickening', 'XPO:0102520', 'abnormal microtubule morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(403206, 'HP:0032523', 'Tendon thickening', 'XPO:0129638', 'increased size of the skeletal subdivision', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(403207, 'HP:0032523', 'Tendon thickening', 'XPO:0102625', 'abnormal ligament cell morphology', 0.4090909090909091, 6.985637650836012, 1.6904913064432443, 'UPHENO:0002712', 'abnormal connective tissue'),
(403208, 'HP:0032523', 'Tendon thickening', 'XPO:0101999', 'abnormal skeletal tissue morphology', 0.4583333333333333, 6.985637650836012, 1.7893436198691701, 'UPHENO:0002712', 'abnormal connective tissue'),
(403209, 'HP:0032523', 'Tendon thickening', 'XPO:0128456', 'decreased size of the vacuolated notochordal tissue', 0.4489795918367347, 6.985637650836012, 1.7709908924643512, 'UPHENO:0002712', 'abnormal connective tissue'),
(403210, 'HP:0032523', 'Tendon thickening', 'XPO:0102567', 'abnormal skeleton morphology', 0.5128205128205128, 4.638757693672553, 1.5423521320759594, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(403211, 'HP:0032523', 'Tendon thickening', 'XPO:0102113', 'abnormal anatomical line morphology', 0.4482758620689655, 2.786899518863159, 1.1177207989108764, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(403212, 'HP:0032523', 'Tendon thickening', 'XPO:0140269', 'abnormally necrotic anatomical line', 0.41935483870967744, 2.786899518863159, 1.0810641970914296, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(403213, 'HP:0032523', 'Tendon thickening', 'XPO:0140144', 'abnormally necrotic portion of organism substance', 0.41935483870967744, 2.786899518863159, 1.0810641970914296, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(403214, 'HP:0032523', 'Tendon thickening', 'XPO:0102048', 'abnormal ligament morphology', 0.43902439024390244, 6.985637650836012, 1.7512467873269968, 'UPHENO:0002712', 'abnormal connective tissue'),
(403215, 'HP:0025720', 'Limited horizontal extraocular movement', 'XPO:0101173', 'abnormal retinal layer', 0.4107142857142857, 6.02624522851634, 1.5732339319278652, 'HP:0000478', 'Abnormality of the eye'),
(403216, 'HP:0025525', 'Scaling skin on fingertip', 'XPO:0101640', 'abnormal epidermis morphology', 0.42857142857142855, 11.189682030596343, 2.189880821668777, 'HP:0011124', 'Abnormal epidermal morphology'),
(403217, 'HP:0025525', 'Scaling skin on fingertip', 'XPO:0140581', 'abnormally necrotic stratum compactum', 0.42, 7.420886955069779, 1.7654383368244009, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(403218, 'HP:0025525', 'Scaling skin on fingertip', 'XPO:0140156', 'abnormally necrotic neuromast mantle cell', 0.42857142857142855, 7.420886955069779, 1.7833620281931915, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(403219, 'HP:0025525', 'Scaling skin on fingertip', 'XPO:0102910', 'abnormal pigment cell morphology', 0.4666666666666667, 7.420886955069779, 1.860935404314874, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(403220, 'HP:0025525', 'Scaling skin on fingertip', 'XPO:0141342', 'decreased pigmentation in the epidermis', 0.4067796610169492, 11.189682030596343, 2.1334795671141142, 'HP:0011124', 'Abnormal epidermal morphology'),
(403221, 'HP:0025525', 'Scaling skin on fingertip', 'XPO:0140235', 'abnormally necrotic stratum spongiosum', 0.42, 7.420886955069779, 1.7654383368244009, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(403222, 'HP:0025525', 'Scaling skin on fingertip', 'XPO:0102954', 'abnormal iridophore morphology', 0.44680851063829785, 7.420886955069779, 1.8209106095604752, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(403223, 'HP:0025525', 'Scaling skin on fingertip', 'XPO:0128647', 'decreased size of the stratum compactum', 0.40384615384615385, 7.420886955069779, 1.7311547172139254, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(403224, 'HP:0025525', 'Scaling skin on fingertip', 'XPO:0115316', 'abnormally neoplastic epidermis', 0.4067796610169492, 11.189682030596343, 2.1334795671141142, 'HP:0011124', 'Abnormal epidermal morphology'),
(403225, 'HP:0025525', 'Scaling skin on fingertip', 'XPO:0115510', 'abnormal degeneration of whole organism', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(403226, 'HP:0025525', 'Scaling skin on fingertip', 'XPO:0140701', 'abnormally necrotic neuromast support cell', 0.42857142857142855, 7.420886955069779, 1.7833620281931915, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(403227, 'HP:0025525', 'Scaling skin on fingertip', 'XPO:0140269', 'abnormally necrotic anatomical line', 0.41935483870967744, 2.786899518863159, 1.0810641970914296, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(403228, 'HP:0025525', 'Scaling skin on fingertip', 'XPO:0102601', 'abnormal disaggregated/reaggregated ectoderm treated with activin morphology', 0.41935483870967744, 2.786899518863159, 1.0810641970914296, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(403229, 'HP:0025525', 'Scaling skin on fingertip', 'XPO:0130356', 'increased size of the skin gland', 0.42, 7.420886955069779, 1.7654383368244009, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(403230, 'HP:0025525', 'Scaling skin on fingertip', 'XPO:0140154', 'abnormally necrotic skin', 0.4375, 7.420886955069779, 1.8018429573198183, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(403231, 'HP:0025525', 'Scaling skin on fingertip', 'XPO:0129655', 'increased size of the skin', 0.42, 7.420886955069779, 1.7654383368244009, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(403232, 'HP:0025525', 'Scaling skin on fingertip', 'XPO:0102113', 'abnormal anatomical line morphology', 0.4482758620689655, 2.786899518863159, 1.1177207989108764, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(403233, 'HP:0025525', 'Scaling skin on fingertip', 'XPO:0102055', 'abnormal process morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(403234, 'HP:0025525', 'Scaling skin on fingertip', 'XPO:0115317', 'abnormally incomplete structure of epidermis', 0.42105263157894735, 11.189682030596343, 2.1705863414096775, 'HP:0011124', 'Abnormal epidermal morphology'),
(403235, 'HP:0025525', 'Scaling skin on fingertip', 'XPO:0130126', 'increased size of the stratum compactum', 0.40384615384615385, 7.420886955069779, 1.7311547172139254, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(403236, 'HP:0025525', 'Scaling skin on fingertip', 'XPO:0102727', 'abnormal skin seromucous gland morphology', 0.4772727272727273, 7.420886955069779, 1.881963590463099, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(403237, 'HP:0025525', 'Scaling skin on fingertip', 'XPO:0140591', 'abnormally necrotic skin gland', 0.4375, 7.420886955069779, 1.8018429573198183, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(403238, 'HP:0025525', 'Scaling skin on fingertip', 'XPO:0102588', 'abnormal centrosome morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(403239, 'HP:0025525', 'Scaling skin on fingertip', 'XPO:0128803', 'decreased size of the dermis', 0.42, 7.420886955069779, 1.7654383368244009, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(403240, 'HP:0025525', 'Scaling skin on fingertip', 'XPO:0141336', 'increased pigmentation in the epidermis', 0.4067796610169492, 11.189682030596343, 2.1334795671141142, 'UPHENO:0020750', 'abnormal skin epidermis morphology'),
(403241, 'HP:0025525', 'Scaling skin on fingertip', 'XPO:0102176', 'abnormal neuromast support cell morphology', 0.4666666666666667, 7.420886955069779, 1.860935404314874, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(403242, 'HP:0025525', 'Scaling skin on fingertip', 'XPO:0101636', 'abnormal cell morphology', 0.4166666666666667, 2.786899518863159, 1.0775936770692605, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(403243, 'HP:0025525', 'Scaling skin on fingertip', 'XPO:0102742', 'abnormal cell-free extract morphology', 0.41935483870967744, 2.786899518863159, 1.0810641970914296, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(403244, 'HP:0025525', 'Scaling skin on fingertip', 'XPO:0101716', 'abnormal anatomical group morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(403245, 'HP:0025525', 'Scaling skin on fingertip', 'XPO:0101638', 'abnormal anatomical structure morphology', 0.4482758620689655, 2.786899518863159, 1.1177207989108764, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(403246, 'HP:0025525', 'Scaling skin on fingertip', 'XPO:0102626', 'abnormal granular gland morphology', 0.4772727272727273, 7.420886955069779, 1.881963590463099, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(403247, 'HP:0025525', 'Scaling skin on fingertip', 'XPO:0130706', 'increased size of the stratum spongiosum', 0.40384615384615385, 7.420886955069779, 1.7311547172139254, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(403248, 'HP:0025525', 'Scaling skin on fingertip', 'XPO:0130281', 'increased size of the dermis', 0.42, 7.420886955069779, 1.7654383368244009, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(403249, 'HP:0025525', 'Scaling skin on fingertip', 'XPO:0101740', 'abnormal cell part morphology', 0.42857142857142855, 2.786899518863159, 1.092879457252359, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(403250, 'HP:0025525', 'Scaling skin on fingertip', 'XPO:0102646', 'abnormal goblet cell morphology', 0.42857142857142855, 7.420886955069779, 1.7833620281931915, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(403251, 'HP:0025525', 'Scaling skin on fingertip', 'XPO:0139718', 'abnormally necrotic anatomical structure', 0.41935483870967744, 2.786899518863159, 1.0810641970914296, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(403252, 'HP:0025525', 'Scaling skin on fingertip', 'XPO:0103147', 'abnormal neuromast mantle cell morphology', 0.4666666666666667, 7.420886955069779, 1.860935404314874, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(403253, 'HP:0025525', 'Scaling skin on fingertip', 'XPO:0103161', 'abnormal skin mucous gland morphology', 0.4375, 7.420886955069779, 1.8018429573198183, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(403254, 'HP:0025525', 'Scaling skin on fingertip', 'XPO:0103019', 'abnormal melanophore morphology', 0.44680851063829785, 7.420886955069779, 1.8209106095604752, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(403255, 'HP:0025525', 'Scaling skin on fingertip', 'XPO:0102703', 'abnormal endoplasmic reticulum morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(403256, 'HP:0025525', 'Scaling skin on fingertip', 'XPO:0102139', 'abnormal skin morphology', 0.5, 7.420886955069779, 1.9262511460178005, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(403257, 'HP:0025525', 'Scaling skin on fingertip', 'XPO:0141277', 'abnormal actin cytoskeleton morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(403258, 'HP:0025525', 'Scaling skin on fingertip', 'XPO:0101976', 'abnormal portion of organism substance morphology', 0.4482758620689655, 2.786899518863159, 1.1177207989108764, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(403259, 'HP:0025525', 'Scaling skin on fingertip', 'XPO:0103179', 'abnormal lampbrush chromosome morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(403260, 'HP:0025525', 'Scaling skin on fingertip', 'XPO:0102886', 'abnormal stratum compactum morphology', 0.4666666666666667, 7.420886955069779, 1.860935404314874, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(403261, 'HP:0025525', 'Scaling skin on fingertip', 'XPO:0141296', 'abnormal adherens junction morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(403262, 'HP:0025525', 'Scaling skin on fingertip', 'XPO:0100507', 'abnormal skin', 0.4166666666666667, 6.8660902472206855, 1.6914109306558096, 'HP:0000951', 'Abnormality of the skin'),
(403263, 'HP:0025525', 'Scaling skin on fingertip', 'XPO:0140481', 'abnormally necrotic melanophore', 0.40384615384615385, 7.420886955069779, 1.7311547172139254, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(403264, 'HP:0025525', 'Scaling skin on fingertip', 'XPO:0101694', 'abnormal anatomical space morphology', 0.41935483870967744, 2.786899518863159, 1.0810641970914296, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(403265, 'HP:0025525', 'Scaling skin on fingertip', 'XPO:0102945', 'abnormal Eberth-Kastschenko layer morphology', 0.4666666666666667, 7.420886955069779, 1.860935404314874, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(403266, 'HP:0025525', 'Scaling skin on fingertip', 'XPO:0103201', 'abnormal activin-induced ectoderm morphology', 0.41935483870967744, 2.786899518863159, 1.0810641970914296, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(403267, 'HP:0025525', 'Scaling skin on fingertip', 'XPO:0140540', 'abnormally necrotic dermis', 0.4375, 7.420886955069779, 1.8018429573198183, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(403268, 'HP:0025525', 'Scaling skin on fingertip', 'XPO:0140698', 'abnormally necrotic xanthophore', 0.40384615384615385, 7.420886955069779, 1.7311547172139254, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(403269, 'HP:0025525', 'Scaling skin on fingertip', 'XPO:0102896', 'abnormal mitotic spindle morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(403270, 'HP:0025525', 'Scaling skin on fingertip', 'XPO:0101890', 'abnormal organ part morphology', 0.41935483870967744, 2.786899518863159, 1.0810641970914296, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(403271, 'HP:0025525', 'Scaling skin on fingertip', 'XPO:0102693', 'abnormal plasma membrane morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(403272, 'HP:0025525', 'Scaling skin on fingertip', 'XPO:0107345', 'abnormal anatomical axis morphology', 0.41935483870967744, 2.786899518863159, 1.0810641970914296, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(403273, 'HP:0025525', 'Scaling skin on fingertip', 'XPO:0128878', 'decreased size of the skin gland', 0.42, 7.420886955069779, 1.7654383368244009, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(403274, 'HP:0025525', 'Scaling skin on fingertip', 'XPO:0141330', 'edematous epidermis', 0.41379310344827586, 11.189682030596343, 2.151793032342996, 'UPHENO:0020750', 'abnormal skin epidermis morphology'),
(403275, 'HP:0025525', 'Scaling skin on fingertip', 'XPO:0102539', 'abnormal cytoplasm morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(403276, 'HP:0025525', 'Scaling skin on fingertip', 'XPO:0140539', 'abnormally necrotic Eberth-Kastschenko layer', 0.42, 7.420886955069779, 1.7654383368244009, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(403277, 'HP:0025525', 'Scaling skin on fingertip', 'XPO:0101642', 'abnormal multicellular anatomical structure morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(403278, 'HP:0025525', 'Scaling skin on fingertip', 'XPO:0102360', 'abnormal cell condensation morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(403279, 'HP:0025525', 'Scaling skin on fingertip', 'XPO:0128513', 'decreased size of the Eberth-Kastschenko layer', 0.40384615384615385, 7.420886955069779, 1.7311547172139254, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(403280, 'HP:0025525', 'Scaling skin on fingertip', 'XPO:0102520', 'abnormal microtubule morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(403281, 'HP:0025525', 'Scaling skin on fingertip', 'XPO:0102773', 'abnormal Keller explant morphology', 0.41935483870967744, 2.786899518863159, 1.0810641970914296, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(403282, 'HP:0025525', 'Scaling skin on fingertip', 'XPO:0140061', 'abnormally necrotic pigment cell', 0.42857142857142855, 7.420886955069779, 1.7833620281931915, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(403283, 'HP:0025525', 'Scaling skin on fingertip', 'XPO:0102356', 'abnormal kinetochore morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(403284, 'HP:0025525', 'Scaling skin on fingertip', 'XPO:0142064', 'abnormal desmosome morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(403285, 'HP:0025525', 'Scaling skin on fingertip', 'XPO:0102353', 'abnormal centromere morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(403286, 'HP:0025525', 'Scaling skin on fingertip', 'XPO:0141057', 'abnormally necrotic iridophore', 0.40384615384615385, 7.420886955069779, 1.7311547172139254, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(403287, 'HP:0025525', 'Scaling skin on fingertip', 'XPO:0141205', 'abnormally necrotic skin seromucous gland', 0.4117647058823529, 7.420886955069779, 1.7480444314835069, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(403288, 'HP:0025525', 'Scaling skin on fingertip', 'XPO:0101713', 'abnormal anatomical entity in vitro morphology', 0.4482758620689655, 2.786899518863159, 1.1177207989108764, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(403289, 'HP:0025525', 'Scaling skin on fingertip', 'XPO:0140144', 'abnormally necrotic portion of organism substance', 0.41935483870967744, 2.786899518863159, 1.0810641970914296, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(403290, 'HP:0025525', 'Scaling skin on fingertip', 'XPO:0129993', 'increased size of the Eberth-Kastschenko layer', 0.40384615384615385, 7.420886955069779, 1.7311547172139254, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(403291, 'HP:0025525', 'Scaling skin on fingertip', 'XPO:0103223', 'abnormal xanthophore morphology', 0.44680851063829785, 7.420886955069779, 1.8209106095604752, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(403292, 'HP:0025525', 'Scaling skin on fingertip', 'XPO:0129230', 'decreased size of the stratum spongiosum', 0.40384615384615385, 7.420886955069779, 1.7311547172139254, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(403293, 'HP:0025525', 'Scaling skin on fingertip', 'XPO:0141219', 'abnormally necrotic granular gland', 0.4117647058823529, 7.420886955069779, 1.7480444314835069, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(403294, 'HP:0025525', 'Scaling skin on fingertip', 'XPO:0141316', 'abnormal anatomical region morphology', 0.41935483870967744, 2.786899518863159, 1.0810641970914296, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(403295, 'HP:0025525', 'Scaling skin on fingertip', 'XPO:0102840', 'abnormal stratum spongiosum morphology', 0.4666666666666667, 7.420886955069779, 1.860935404314874, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(403296, 'HP:0025525', 'Scaling skin on fingertip', 'XPO:0102526', 'abnormal nucleus morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(403297, 'HP:0025525', 'Scaling skin on fingertip', 'XPO:0102381', 'abnormal mucociliary epithelium morphology', 0.4074074074074074, 8.516821552129047, 1.8627442626148192, 'UPHENO:0087435', 'abnormal skin epidermis morphology'),
(403298, 'HP:0025525', 'Scaling skin on fingertip', 'XPO:0102178', 'abnormal whole organism morphology', 0.41935483870967744, 2.786899518863159, 1.0810641970914296, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(403299, 'HP:0025525', 'Scaling skin on fingertip', 'XPO:0128175', 'decreased size of the skin', 0.42, 7.420886955069779, 1.7654383368244009, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(403300, 'HP:0025525', 'Scaling skin on fingertip', 'XPO:0103145', 'abnormal basal body morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(403301, 'HP:0025525', 'Scaling skin on fingertip', 'XPO:0101871', 'abnormal acellular anatomical structure morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(403302, 'HP:0025525', 'Scaling skin on fingertip', 'XPO:0107399', 'abnormal filopodium morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(403303, 'HP:0025525', 'Scaling skin on fingertip', 'XPO:0102561', 'abnormal dermis morphology', 0.4883720930232558, 7.420886955069779, 1.9037211177944116, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(403304, 'HP:0025525', 'Scaling skin on fingertip', 'XPO:0102615', 'abnormal skin gland morphology', 0.5, 7.420886955069779, 1.9262511460178005, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(403305, 'HP:0025525', 'Scaling skin on fingertip', 'XPO:0100983', 'abnormal skin gland', 0.40540540540540543, 6.8660902472206855, 1.6683974647021622, 'HP:0000951', 'Abnormality of the skin'),
(403306, 'HP:0030757', 'Tooth abscess', 'XPO:0140890', 'abnormally necrotic dentine', 0.4791666666666667, 11.200822588201543, 2.316691784315134, 'HP:0011061', 'Abnormality of dental structure'),
(403307, 'HP:0030757', 'Tooth abscess', 'XPO:0129449', 'decreased size of the dentine', 0.46938775510204084, 11.200822588201543, 2.2929302148064066, 'HP:0011061', 'Abnormality of dental structure'),
(403308, 'HP:0030757', 'Tooth abscess', 'XPO:0101567', 'abnormal tongue', 0.5161290322580645, 7.884497199543557, 2.017279829235854, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(403309, 'HP:0030757', 'Tooth abscess', 'XPO:0128510', 'decreased size of the cementum', 0.4842105263157895, 11.200822588201543, 2.3288529796023734, 'HP:0011061', 'Abnormality of dental structure'),
(403310, 'HP:0030757', 'Tooth abscess', 'XPO:0102279', 'abnormal mouth morphology', 0.4852941176470588, 7.312692920701687, 1.8838277146745184, 'UPHENO:0076800', 'abnormal mouth morphology'),
(403311, 'HP:0030757', 'Tooth abscess', 'XPO:0103138', 'abnormal upper jaw morphology', 0.475, 7.312692920701687, 1.8637406303810895, 'UPHENO:0076800', 'abnormal mouth morphology'),
(403312, 'HP:0030757', 'Tooth abscess', 'XPO:0131611', 'increased size of the roof of mouth', 0.4230769230769231, 7.312692920701687, 1.7589291117884391, 'UPHENO:0076800', 'abnormal mouth morphology'),
(403313, 'HP:0030757', 'Tooth abscess', 'XPO:0129990', 'increased size of the cementum', 0.4842105263157895, 11.200822588201543, 2.3288529796023734, 'HP:0011061', 'Abnormality of dental structure'),
(403314, 'HP:0030757', 'Tooth abscess', 'XPO:0101659', 'abnormal lower jaw morphology', 0.48717948717948717, 7.312692920701687, 1.8874835064202586, 'UPHENO:0076800', 'abnormal mouth morphology'),
(403315, 'HP:0030757', 'Tooth abscess', 'XPO:0141006', 'abnormally necrotic cementum', 0.4946236559139785, 11.200822588201543, 2.35376120662656, 'HP:0011061', 'Abnormality of dental structure'),
(403316, 'HP:0030757', 'Tooth abscess', 'XPO:0102890', 'abnormal dentine morphology', 0.5287356321839081, 11.200822588201543, 2.433572273870768, 'HP:0011061', 'Abnormality of dental structure'),
(403317, 'HP:0030757', 'Tooth abscess', 'XPO:0130701', 'increased size of the upper jaw', 0.4367816091954023, 7.312692920701687, 1.7871904715099365, 'UPHENO:0076800', 'abnormal mouth morphology'),
(403318, 'HP:0030757', 'Tooth abscess', 'XPO:0102861', 'abnormal cementum morphology', 0.5411764705882353, 11.200822588201543, 2.4620360752775117, 'HP:0011061', 'Abnormality of dental structure'),
(403319, 'HP:0030757', 'Tooth abscess', 'XPO:0102103', 'abnormal mandibular arch morphology', 0.41025641025641024, 5.725717590856133, 1.5326488002692003, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(403320, 'HP:0030757', 'Tooth abscess', 'XPO:0129585', 'increased size of the tongue', 0.4235294117647059, 7.884497199543557, 1.8273796707261338, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(403321, 'HP:0030757', 'Tooth abscess', 'XPO:0126089', 'absent tongue', 0.44594594594594594, 7.884497199543557, 1.8751158796081413, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(403322, 'HP:0030757', 'Tooth abscess', 'XPO:0140639', 'abnormally necrotic upper jaw', 0.4470588235294118, 7.312692920701687, 1.8080939947803472, 'UPHENO:0076800', 'abnormal mouth morphology'),
(403323, 'HP:0030757', 'Tooth abscess', 'XPO:0140789', 'abnormally necrotic roof of mouth', 0.4342105263157895, 7.312692920701687, 1.7819226251113227, 'UPHENO:0076800', 'abnormal mouth morphology'),
(403324, 'HP:0030757', 'Tooth abscess', 'XPO:0129152', 'decreased size of the oral cavity', 0.4794520547945205, 7.884497199543557, 1.9442835141364547, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(403325, 'HP:0030757', 'Tooth abscess', 'XPO:0130923', 'increased size of the dentine', 0.46938775510204084, 11.200822588201543, 2.2929302148064066, 'HP:0011061', 'Abnormality of dental structure'),
(403326, 'HP:0030757', 'Tooth abscess', 'XPO:0128105', 'decreased size of the tongue', 0.43209876543209874, 7.884497199543557, 1.8457739585267778, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(403327, 'HP:0030757', 'Tooth abscess', 'XPO:0102960', 'abnormal oral epithelium morphology', 0.42857142857142855, 7.312692920701687, 1.7703138850862843, 'UPHENO:0076800', 'abnormal mouth morphology'),
(403328, 'HP:0030757', 'Tooth abscess', 'XPO:0129225', 'decreased size of the upper jaw', 0.4367816091954023, 7.312692920701687, 1.7871904715099365, 'UPHENO:0076800', 'abnormal mouth morphology'),
(403329, 'HP:0030757', 'Tooth abscess', 'XPO:0141311', 'abnormal roof of mouth morphology', 0.4647887323943662, 7.312692920701687, 1.8435990000545652, 'UPHENO:0076800', 'abnormal mouth morphology'),
(403330, 'HP:0030757', 'Tooth abscess', 'XPO:0103096', 'abnormal oral cavity morphology', 0.5147058823529411, 7.884497199543557, 2.0144967331818533, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(403331, 'HP:0030757', 'Tooth abscess', 'XPO:0140626', 'abnormally necrotic tongue', 0.4794520547945205, 7.884497199543557, 1.9442835141364547, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(403332, 'HP:0030757', 'Tooth abscess', 'XPO:0127750', 'abnormally localised tongue', 0.4583333333333333, 7.884497199543557, 1.9009807687412648, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(403333, 'HP:0030757', 'Tooth abscess', 'XPO:0130628', 'increased size of the oral cavity', 0.4794520547945205, 7.884497199543557, 1.9442835141364547, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(403334, 'HP:0030757', 'Tooth abscess', 'XPO:0128989', 'decreased size of the tooth', 0.5056179775280899, 9.872199840740173, 2.2341803233463895, 'HP:0006482', 'Abnormal dental morphology'),
(403335, 'HP:0030757', 'Tooth abscess', 'XPO:0130358', 'increased size of the lower jaw', 0.4470588235294118, 7.312692920701687, 1.8080939947803472, 'UPHENO:0076800', 'abnormal mouth morphology'),
(403336, 'HP:0030757', 'Tooth abscess', 'XPO:0103735', 'increased size of the mouth', 0.45454545454545453, 7.884497199543557, 1.8931091789510952, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(403337, 'HP:0030757', 'Tooth abscess', 'XPO:0115558', 'abnormally incomplete structure of mouth', 0.4782608695652174, 7.312692920701687, 1.8701269676463677, 'UPHENO:0076800', 'abnormal mouth morphology'),
(403338, 'HP:0030757', 'Tooth abscess', 'XPO:0128880', 'decreased size of the lower jaw', 0.4470588235294118, 7.312692920701687, 1.8080939947803472, 'UPHENO:0076800', 'abnormal mouth morphology'),
(403339, 'HP:0030757', 'Tooth abscess', 'XPO:0103352', 'decreased size of the mouth', 0.45454545454545453, 7.884497199543557, 1.8931091789510952, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(403340, 'HP:0030757', 'Tooth abscess', 'XPO:0139736', 'abnormally necrotic tooth', 0.5294117647058824, 9.872199840740173, 2.286144951488288, 'HP:0006482', 'Abnormal dental morphology'),
(403341, 'HP:0030757', 'Tooth abscess', 'XPO:0131573', 'decreased size of the roof of mouth', 0.4230769230769231, 7.312692920701687, 1.7589291117884391, 'UPHENO:0076800', 'abnormal mouth morphology'),
(403342, 'HP:0030757', 'Tooth abscess', 'XPO:0115393', 'abnormally decreased volume of oral cavity', 0.4666666666666667, 7.884497199543557, 1.9181845652735452, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(403343, 'HP:0030757', 'Tooth abscess', 'XPO:0141830', 'increased width of mouth', 0.4268292682926829, 7.884497199543557, 1.8344847152639032, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(403344, 'HP:0030757', 'Tooth abscess', 'XPO:0101816', 'abnormal tooth morphology', 0.5844155844155844, 9.872199840740173, 2.401971573394158, 'HP:0006482', 'Abnormal dental morphology'),
(403345, 'HP:0030757', 'Tooth abscess', 'XPO:0103828', 'decreased width of the mouth', 0.4268292682926829, 7.884497199543557, 1.8344847152639032, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(403346, 'HP:0030757', 'Tooth abscess', 'XPO:0130466', 'increased size of the tooth', 0.5056179775280899, 9.872199840740173, 2.2341803233463895, 'HP:0006482', 'Abnormal dental morphology'),
(403347, 'HP:0030757', 'Tooth abscess', 'XPO:0140897', 'abnormally necrotic lower jaw', 0.4578313253012048, 7.312692920701687, 1.8297485869390886, 'UPHENO:0076800', 'abnormal mouth morphology'),
(403348, 'HP:0030757', 'Tooth abscess', 'XPO:0103199', 'abnormal tongue morphology', 0.5147058823529411, 7.884497199543557, 2.0144967331818533, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(403349, 'HP:0031392', 'Abnormal proportion of CD4-positive T cells', 'XPO:0131005', 'abnormally increased number of thymocyte', 0.48936170212765956, 9.586341000560333, 2.1659150835640752, 'HP:0011839', 'Abnormal T cell count'),
(403350, 'HP:0031392', 'Abnormal proportion of CD4-positive T cells', 'XPO:0131221', 'abnormally decreased number of thymocyte', 0.4842105263157895, 9.586341000560333, 2.1544853727338116, 'HP:0011839', 'Abnormal T cell count'),
(403351, 'HP:0031392', 'Abnormal proportion of CD4-positive T cells', 'XPO:0125284', 'absent thymocyte', 0.5411764705882353, 9.586341000560333, 2.277696684929434, 'HP:0011839', 'Abnormal T cell count'),
(403352, 'HP:0034194', 'Suprabasal cleavage', 'XPO:0101313', 'abnormal Eberth-Kastschenko layer', 0.4166666666666667, 6.8660902472206855, 1.6914109306558096, 'HP:0000951', 'Abnormality of the skin'),
(403353, 'HP:0034194', 'Suprabasal cleavage', 'XPO:0101095', 'abnormal skin seromucous gland', 0.4411764705882353, 6.8660902472206855, 1.740447489012273, 'HP:0000951', 'Abnormality of the skin'),
(403354, 'HP:0034194', 'Suprabasal cleavage', 'XPO:0100507', 'abnormal skin', 0.46875, 6.8660902472206855, 1.7940122082596586, 'HP:0000951', 'Abnormality of the skin'),
(403355, 'HP:0034194', 'Suprabasal cleavage', 'XPO:0101591', 'abnormal xanthophore', 0.40540540540540543, 6.8660902472206855, 1.6683974647021622, 'HP:0000951', 'Abnormality of the skin'),
(403356, 'HP:0034194', 'Suprabasal cleavage', 'XPO:0101529', 'abnormal skin mucous gland', 0.4166666666666667, 6.8660902472206855, 1.6914109306558096, 'HP:0000951', 'Abnormality of the skin'),
(403357, 'HP:0034194', 'Suprabasal cleavage', 'XPO:0102615', 'abnormal skin gland morphology', 0.43902439024390244, 7.420886955069779, 1.8049793268950312, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(403358, 'HP:0034194', 'Suprabasal cleavage', 'XPO:0101254', 'abnormal stratum compactum', 0.4166666666666667, 6.8660902472206855, 1.6914109306558096, 'HP:0000951', 'Abnormality of the skin'),
(403359, 'HP:0034194', 'Suprabasal cleavage', 'XPO:0102910', 'abnormal pigment cell morphology', 0.4090909090909091, 7.420886955069779, 1.7423597190908553, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(403360, 'HP:0034194', 'Suprabasal cleavage', 'XPO:0100983', 'abnormal skin gland', 0.45454545454545453, 6.8660902472206855, 1.7666211003984522, 'HP:0000951', 'Abnormality of the skin'),
(403361, 'HP:0034194', 'Suprabasal cleavage', 'XPO:0102561', 'abnormal dermis morphology', 0.42857142857142855, 7.420886955069779, 1.7833620281931915, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(403362, 'HP:0034194', 'Suprabasal cleavage', 'XPO:0102886', 'abnormal stratum compactum morphology', 0.4090909090909091, 7.420886955069779, 1.7423597190908553, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(403363, 'HP:0034194', 'Suprabasal cleavage', 'XPO:0102139', 'abnormal skin morphology', 0.43902439024390244, 7.420886955069779, 1.8049793268950312, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(403364, 'HP:0034194', 'Suprabasal cleavage', 'XPO:0100994', 'abnormal granular gland', 0.4411764705882353, 6.8660902472206855, 1.740447489012273, 'HP:0000951', 'Abnormality of the skin'),
(403365, 'HP:0034194', 'Suprabasal cleavage', 'XPO:0103147', 'abnormal neuromast mantle cell morphology', 0.4090909090909091, 7.420886955069779, 1.7423597190908553, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(403366, 'HP:0034194', 'Suprabasal cleavage', 'XPO:0101322', 'abnormal iridophore', 0.40540540540540543, 6.8660902472206855, 1.6683974647021622, 'HP:0000951', 'Abnormality of the skin'),
(403367, 'HP:0034194', 'Suprabasal cleavage', 'XPO:0102840', 'abnormal stratum spongiosum morphology', 0.4090909090909091, 7.420886955069779, 1.7423597190908553, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(403368, 'HP:0034194', 'Suprabasal cleavage', 'XPO:0101387', 'abnormal melanophore', 0.40540540540540543, 6.8660902472206855, 1.6683974647021622, 'HP:0000951', 'Abnormality of the skin'),
(403369, 'HP:0034194', 'Suprabasal cleavage', 'XPO:0101208', 'abnormal stratum spongiosum', 0.4166666666666667, 6.8660902472206855, 1.6914109306558096, 'HP:0000951', 'Abnormality of the skin'),
(403370, 'HP:0034194', 'Suprabasal cleavage', 'XPO:0102626', 'abnormal granular gland morphology', 0.4186046511627907, 7.420886955069779, 1.7625032752155354, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(403371, 'HP:0034194', 'Suprabasal cleavage', 'XPO:0100929', 'abnormal dermis', 0.4411764705882353, 6.8660902472206855, 1.740447489012273, 'HP:0000951', 'Abnormality of the skin'),
(403372, 'HP:0034194', 'Suprabasal cleavage', 'XPO:0100544', 'abnormal neuromast support cell', 0.4166666666666667, 6.8660902472206855, 1.6914109306558096, 'HP:0000951', 'Abnormality of the skin'),
(403373, 'HP:0034194', 'Suprabasal cleavage', 'XPO:0102727', 'abnormal skin seromucous gland morphology', 0.4186046511627907, 7.420886955069779, 1.7625032752155354, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(403374, 'HP:0034194', 'Suprabasal cleavage', 'XPO:0102176', 'abnormal neuromast support cell morphology', 0.4090909090909091, 7.420886955069779, 1.7423597190908553, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(403375, 'HP:0034194', 'Suprabasal cleavage', 'XPO:0101515', 'abnormal neuromast mantle cell', 0.4166666666666667, 6.8660902472206855, 1.6914109306558096, 'HP:0000951', 'Abnormality of the skin'),
(403376, 'HP:0034194', 'Suprabasal cleavage', 'XPO:0101278', 'abnormal pigment cell', 0.4166666666666667, 6.8660902472206855, 1.6914109306558096, 'HP:0000951', 'Abnormality of the skin'),
(403377, 'HP:0034194', 'Suprabasal cleavage', 'XPO:0102945', 'abnormal Eberth-Kastschenko layer morphology', 0.4090909090909091, 7.420886955069779, 1.7423597190908553, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(403378, 'HP:0006217', 'Limited mobility of proximal interphalangeal joint', 'XPO:0129188', 'decreased size of the forelimb digit 2', 0.4017094017094017, 7.492661022682715, 1.734898376457027, 'HP:0001167', 'Abnormal finger morphology'),
(403379, 'HP:0006217', 'Limited mobility of proximal interphalangeal joint', 'XPO:0115786', 'duplicated forelimb digit 2 in regenerating forelimb', 0.44881889763779526, 7.774297771301195, 1.8679538954758415, 'HP:0005918', 'Abnormal finger phalanx morphology'),
(403380, 'HP:0006217', 'Limited mobility of proximal interphalangeal joint', 'XPO:0103609', 'abnormally increased number of forelimb digit in the regenerating forelimb', 0.4672131147540984, 7.774297771301195, 1.9058472857906208, 'HP:0005918', 'Abnormal finger phalanx morphology'),
(403381, 'HP:0006217', 'Limited mobility of proximal interphalangeal joint', 'XPO:0129161', 'decreased size of the forelimb digit 5', 0.4017094017094017, 7.492661022682715, 1.734898376457027, 'HP:0001167', 'Abnormal finger morphology'),
(403382, 'HP:0006217', 'Limited mobility of proximal interphalangeal joint', 'XPO:0140716', 'abnormally necrotic forelimb digit 4', 0.41228070175438597, 7.492661022682715, 1.7575777491876043, 'HP:0001167', 'Abnormal finger morphology'),
(403383, 'HP:0006217', 'Limited mobility of proximal interphalangeal joint', 'XPO:0103432', 'decreased size of the forelimb digit', 0.41228070175438597, 7.492661022682715, 1.7575777491876043, 'HP:0001167', 'Abnormal finger morphology'),
(403384, 'HP:0006217', 'Limited mobility of proximal interphalangeal joint', 'XPO:0130664', 'increased size of the forelimb digit 2', 0.4051724137931034, 7.492661022682715, 1.7423603393941962, 'HP:0001167', 'Abnormal finger morphology'),
(403385, 'HP:0006217', 'Limited mobility of proximal interphalangeal joint', 'XPO:0103755', 'increased size of the forelimb digit', 0.415929203539823, 7.492661022682715, 1.7653375120804229, 'HP:0001167', 'Abnormal finger morphology'),
(403386, 'HP:0006217', 'Limited mobility of proximal interphalangeal joint', 'XPO:0102598', 'abnormal forelimb digit 3 morphology', 0.44761904761904764, 7.492661022682715, 1.8313540867635612, 'HP:0001167', 'Abnormal finger morphology'),
(403387, 'HP:0006217', 'Limited mobility of proximal interphalangeal joint', 'XPO:0140219', 'abnormally necrotic forelimb digit', 0.42342342342342343, 7.492661022682715, 1.781170452476563, 'HP:0001167', 'Abnormal finger morphology'),
(403388, 'HP:0006217', 'Limited mobility of proximal interphalangeal joint', 'XPO:0128172', 'decreased size of the forelimb digit 3', 0.4017094017094017, 7.492661022682715, 1.734898376457027, 'HP:0001167', 'Abnormal finger morphology'),
(403389, 'HP:0006217', 'Limited mobility of proximal interphalangeal joint', 'XPO:0133358', 'fused forelimb digits', 0.41964285714285715, 7.492661022682715, 1.7732009697610411, 'HP:0001167', 'Abnormal finger morphology'),
(403390, 'HP:0006217', 'Limited mobility of proximal interphalangeal joint', 'XPO:0129652', 'increased size of the forelimb digit 3', 0.4051724137931034, 7.492661022682715, 1.7423603393941962, 'HP:0001167', 'Abnormal finger morphology'),
(403391, 'HP:0006217', 'Limited mobility of proximal interphalangeal joint', 'XPO:0141556', 'abnormal forelimb digit morphology in the regenerating forelimb', 0.43119266055045874, 7.492661022682715, 1.7974371869340195, 'HP:0001167', 'Abnormal finger morphology'),
(403392, 'HP:0006217', 'Limited mobility of proximal interphalangeal joint', 'XPO:0102746', 'abnormal forelimb digit 2 morphology', 0.44761904761904764, 7.492661022682715, 1.8313540867635612, 'HP:0001167', 'Abnormal finger morphology'),
(403393, 'HP:0006217', 'Limited mobility of proximal interphalangeal joint', 'XPO:0103634', 'abnormally increased number of forelimb digit', 0.49137931034482757, 7.774297771301195, 1.954515049130426, 'HP:0005918', 'Abnormal finger phalanx morphology'),
(403394, 'HP:0006217', 'Limited mobility of proximal interphalangeal joint', 'XPO:0102214', 'abnormal forelimb digit morphology', 0.4563106796116505, 7.492661022682715, 1.8490487401256015, 'HP:0001167', 'Abnormal finger morphology'),
(403395, 'HP:0006217', 'Limited mobility of proximal interphalangeal joint', 'XPO:0115788', 'duplicated forelimb digit 4 in regenerating forelimb', 0.44881889763779526, 7.774297771301195, 1.8679538954758415, 'HP:0005918', 'Abnormal finger phalanx morphology'),
(403396, 'HP:0006217', 'Limited mobility of proximal interphalangeal joint', 'XPO:0141143', 'abnormally necrotic forelimb digit 3', 0.41228070175438597, 7.492661022682715, 1.7575777491876043, 'HP:0001167', 'Abnormal finger morphology'),
(403397, 'HP:0006217', 'Limited mobility of proximal interphalangeal joint', 'XPO:0140898', 'abnormally necrotic forelimb digit 5', 0.41228070175438597, 7.492661022682715, 1.7575777491876043, 'HP:0001167', 'Abnormal finger morphology'),
(403398, 'HP:0006217', 'Limited mobility of proximal interphalangeal joint', 'XPO:0102529', 'abnormal forelimb digit 4 morphology', 0.44761904761904764, 7.492661022682715, 1.8313540867635612, 'HP:0001167', 'Abnormal finger morphology'),
(403399, 'HP:0006217', 'Limited mobility of proximal interphalangeal joint', 'XPO:0102787', 'abnormal forelimb digit 5 morphology', 0.44761904761904764, 7.492661022682715, 1.8313540867635612, 'HP:0001167', 'Abnormal finger morphology'),
(403400, 'HP:0006217', 'Limited mobility of proximal interphalangeal joint', 'XPO:0129148', 'decreased size of the forelimb digit 4', 0.4017094017094017, 7.492661022682715, 1.734898376457027, 'HP:0001167', 'Abnormal finger morphology'),
(403401, 'HP:0006217', 'Limited mobility of proximal interphalangeal joint', 'XPO:0141108', 'abnormally necrotic forelimb digit 2', 0.41228070175438597, 7.492661022682715, 1.7575777491876043, 'HP:0001167', 'Abnormal finger morphology'),
(403402, 'HP:0006217', 'Limited mobility of proximal interphalangeal joint', 'XPO:0130637', 'increased size of the forelimb digit 5', 0.4051724137931034, 7.492661022682715, 1.7423603393941962, 'HP:0001167', 'Abnormal finger morphology'),
(403403, 'HP:0006217', 'Limited mobility of proximal interphalangeal joint', 'XPO:0115787', 'duplicated forelimb digit 3 in regenerating forelimb', 0.44881889763779526, 7.774297771301195, 1.8679538954758415, 'HP:0005918', 'Abnormal finger phalanx morphology'),
(403404, 'HP:0006217', 'Limited mobility of proximal interphalangeal joint', 'XPO:0115789', 'duplicated forelimb digit 5 in regenerating forelimb', 0.44881889763779526, 7.774297771301195, 1.8679538954758415, 'HP:0005918', 'Abnormal finger phalanx morphology'),
(403405, 'HP:0006217', 'Limited mobility of proximal interphalangeal joint', 'XPO:0130624', 'increased size of the forelimb digit 4', 0.4051724137931034, 7.492661022682715, 1.7423603393941962, 'HP:0001167', 'Abnormal finger morphology'),
(403406, 'HP:0033504', 'Elevated circulating fumarate concentration', 'XPO:0141858', 'abnormal serine family amino acid metabolic process', 0.6481481481481481, 9.119292702704945, 2.4311833903840183, 'HP:0004354', 'Abnormal circulating carboxylic acid concentration'),
(403407, 'HP:0033504', 'Elevated circulating fumarate concentration', 'XPO:0141853', 'abnormal glutamate metabolic process', 0.6428571428571429, 12.688487887567785, 2.8560260976712537, 'UPHENO:0078584', 'abnormal dicarboxylic acid metabolic process'),
(403408, 'HP:0033504', 'Elevated circulating fumarate concentration', 'XPO:0141896', 'abnormal lysine metabolic process', 0.6363636363636364, 9.119292702704945, 2.4089803372708736, 'HP:0004354', 'Abnormal circulating carboxylic acid concentration'),
(403409, 'HP:0033504', 'Elevated circulating fumarate concentration', 'XPO:0141889', 'abnormal homoserine metabolic process', 0.625, 9.119292702704945, 2.387374696018744, 'HP:0004354', 'Abnormal circulating carboxylic acid concentration'),
(403410, 'HP:0033504', 'Elevated circulating fumarate concentration', 'XPO:0141873', 'abnormal tricarboxylic acid metabolic process', 0.7291666666666666, 9.119292702704945, 2.5786593924729613, 'HP:0004354', 'Abnormal circulating carboxylic acid concentration'),
(403411, 'HP:0033504', 'Elevated circulating fumarate concentration', 'XPO:0141918', 'abnormal tyrosine metabolic process', 0.6363636363636364, 9.119292702704945, 2.4089803372708736, 'HP:0004354', 'Abnormal circulating carboxylic acid concentration'),
(403412, 'HP:0033504', 'Elevated circulating fumarate concentration', 'XPO:0141917', 'abnormal tryptophan metabolic process', 0.6363636363636364, 9.119292702704945, 2.4089803372708736, 'HP:0004354', 'Abnormal circulating carboxylic acid concentration'),
(403413, 'HP:0033504', 'Elevated circulating fumarate concentration', 'XPO:0141868', 'abnormal asparagine metabolic process', 0.6363636363636364, 9.119292702704945, 2.4089803372708736, 'HP:0004354', 'Abnormal circulating carboxylic acid concentration'),
(403414, 'HP:0033504', 'Elevated circulating fumarate concentration', 'XPO:0141895', 'abnormal leucine metabolic process', 0.6363636363636364, 9.119292702704945, 2.4089803372708736, 'HP:0004354', 'Abnormal circulating carboxylic acid concentration'),
(403415, 'HP:0033504', 'Elevated circulating fumarate concentration', 'XPO:0141857', 'abnormal glycine metabolic process', 0.625, 9.119292702704945, 2.387374696018744, 'HP:0004354', 'Abnormal circulating carboxylic acid concentration'),
(403416, 'HP:0033504', 'Elevated circulating fumarate concentration', 'XPO:0141912', 'abnormal D-serine metabolic process', 0.625, 9.119292702704945, 2.387374696018744, 'HP:0004354', 'Abnormal circulating carboxylic acid concentration'),
(403417, 'HP:0033504', 'Elevated circulating fumarate concentration', 'XPO:0141882', 'abnormal gamma-aminobutyric acid metabolic process', 0.660377358490566, 9.119292702704945, 2.4540119042732016, 'HP:0004354', 'Abnormal circulating carboxylic acid concentration'),
(403418, 'HP:0033504', 'Elevated circulating fumarate concentration', 'XPO:0141869', 'abnormal alpha-amino acid metabolic process', 0.6730769230769231, 9.119292702704945, 2.4774958068530575, 'HP:0004354', 'Abnormal circulating carboxylic acid concentration'),
(403419, 'HP:0033504', 'Elevated circulating fumarate concentration', 'XPO:0141922', 'abnormal valine metabolic process', 0.6363636363636364, 9.119292702704945, 2.4089803372708736, 'HP:0004354', 'Abnormal circulating carboxylic acid concentration'),
(403420, 'HP:0033504', 'Elevated circulating fumarate concentration', 'XPO:0141888', 'abnormal threonine metabolic process', 0.6363636363636364, 9.119292702704945, 2.4089803372708736, 'HP:0004354', 'Abnormal circulating carboxylic acid concentration'),
(403421, 'HP:0033504', 'Elevated circulating fumarate concentration', 'XPO:0141887', 'abnormal histidine metabolic process', 0.6363636363636364, 9.119292702704945, 2.4089803372708736, 'HP:0004354', 'Abnormal circulating carboxylic acid concentration'),
(403422, 'HP:0033504', 'Elevated circulating fumarate concentration', 'XPO:0141847', 'abnormal arginine metabolic process', 0.6363636363636364, 9.119292702704945, 2.4089803372708736, 'HP:0004354', 'Abnormal circulating carboxylic acid concentration'),
(403423, 'HP:0033504', 'Elevated circulating fumarate concentration', 'XPO:0141843', 'abnormal alanine metabolic process', 0.6481481481481481, 9.119292702704945, 2.4311833903840183, 'HP:0004354', 'Abnormal circulating carboxylic acid concentration'),
(403424, 'HP:0033504', 'Elevated circulating fumarate concentration', 'XPO:0141848', 'abnormal proline metabolic process', 0.6363636363636364, 9.119292702704945, 2.4089803372708736, 'HP:0004354', 'Abnormal circulating carboxylic acid concentration'),
(403425, 'HP:0033504', 'Elevated circulating fumarate concentration', 'XPO:0141866', 'abnormal dicarboxylic acid metabolic process', 0.4090909090909091, 12.688487887567785, 2.2783206633207045, 'UPHENO:0078584', 'abnormal dicarboxylic acid metabolic process'),
(403426, 'HP:0033504', 'Elevated circulating fumarate concentration', 'XPO:0141893', 'abnormal isoleucine metabolic process', 0.6363636363636364, 9.119292702704945, 2.4089803372708736, 'HP:0004354', 'Abnormal circulating carboxylic acid concentration'),
(403427, 'HP:0033504', 'Elevated circulating fumarate concentration', 'XPO:0141913', 'abnormal L-serine metabolic process', 0.625, 9.119292702704945, 2.387374696018744, 'HP:0004354', 'Abnormal circulating carboxylic acid concentration'),
(403428, 'HP:0033504', 'Elevated circulating fumarate concentration', 'XPO:0141905', 'abnormal ornithine metabolic process', 0.6481481481481481, 9.119292702704945, 2.4311833903840183, 'HP:0004354', 'Abnormal circulating carboxylic acid concentration'),
(403429, 'HP:0009031', 'Amyotrophy of ankle musculature', 'XPO:0100768', 'abnormal pectoral girdle', 0.4375, 9.463856994035337, 2.0348064858581663, 'UPHENO:0002647', 'abnormal musculature of limb'),
(403430, 'HP:0001762', 'Talipes equinovarus', 'XPO:0100852', 'abnormal interdigital region', 0.4482758620689655, 5.504475013697824, 1.570835217966058, 'HP:0040064', 'Abnormality of limbs'),
(403431, 'HP:0001762', 'Talipes equinovarus', 'XPO:0100386', 'abnormal limb', 0.41935483870967744, 5.504475013697824, 1.5193183443737854, 'HP:0040064', 'Abnormality of limbs'),
(403432, 'HP:0001762', 'Talipes equinovarus', 'XPO:0102484', 'abnormal interdigital region morphology', 0.4444444444444444, 6.173473740856008, 1.656431739326168, 'UPHENO:0087006', 'abnormal autopod region morphology'),
(403433, 'HP:0001762', 'Talipes equinovarus', 'XPO:0100205', 'abnormal limb segment', 0.40625, 5.504475013697824, 1.4953905758412218, 'HP:0040064', 'Abnormality of limbs'),
(403434, 'HP:0011599', 'Mesocardia', 'XPO:0102800', 'abnormal circulating cell morphology', 0.4358974358974359, 5.9590888072311134, 1.6116921329326988, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(403435, 'HP:0011599', 'Mesocardia', 'XPO:0101770', 'abnormal trunk vasculature morphology', 0.4146341463414634, 5.9590888072311134, 1.57189112236161, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(403436, 'HP:0011599', 'Mesocardia', 'XPO:0103024', 'abnormal sinus venosus morphology', 0.40425531914893614, 7.414388317771038, 1.7312729177384698, 'UPHENO:0076810', 'abnormal heart morphology'),
(403437, 'HP:0011599', 'Mesocardia', 'XPO:0101713', 'abnormal anatomical entity in vitro morphology', 0.4230769230769231, 2.485033483301678, 1.0253586298746415, 'UPHENO:0076692', 'abnormal anatomical entity morphology'),
(403438, 'HP:0011599', 'Mesocardia', 'XPO:0100004', 'abnormal cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(403439, 'HP:0011599', 'Mesocardia', 'XPO:0100043', 'abnormal vein', 0.4117647058823529, 5.249153838287537, 1.4701755971154233, 'UPHENO:0080362', 'abnormal cardiovascular system'),
(403440, 'HP:0011599', 'Mesocardia', 'XPO:0101919', 'abnormal heart primordium morphology', 0.4358974358974359, 5.9590888072311134, 1.6116921329326988, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(403441, 'HP:0011599', 'Mesocardia', 'XPO:0141328', 'edematous circulatory system', 0.4594594594594595, 5.9590888072311134, 1.6546781325204374, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(403442, 'HP:0011599', 'Mesocardia', 'XPO:0102649', 'abnormal outflow tract morphology', 0.40425531914893614, 7.414388317771038, 1.7312729177384698, 'UPHENO:0076810', 'abnormal heart morphology'),
(403443, 'HP:0011599', 'Mesocardia', 'XPO:0101740', 'abnormal cell part morphology', 0.40625, 2.485033483301678, 1.004761092295729, 'UPHENO:0076692', 'abnormal anatomical entity morphology'),
(403444, 'HP:0011599', 'Mesocardia', 'XPO:0140420', 'abnormally necrotic bulbous arteriosis', 0.40476190476190477, 5.9590888072311134, 1.5530653998657664, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(403445, 'HP:0011599', 'Mesocardia', 'XPO:0100792', 'abnormal capillary', 0.4117647058823529, 5.249153838287537, 1.4701755971154233, 'UPHENO:0080362', 'abnormal cardiovascular system'),
(403446, 'HP:0011599', 'Mesocardia', 'XPO:0128032', 'decreased size of the cardiovascular system', 0.40476190476190477, 5.9590888072311134, 1.5530653998657664, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(403447, 'HP:0011599', 'Mesocardia', 'XPO:0100780', 'abnormal vascular plexus', 0.4117647058823529, 5.249153838287537, 1.4701755971154233, 'UPHENO:0080362', 'abnormal cardiovascular system'),
(403448, 'HP:0011599', 'Mesocardia', 'XPO:0101900', 'abnormal circulatory system morphology', 0.5, 5.9590888072311134, 1.7261356851694936, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(403449, 'HP:0011599', 'Mesocardia', 'XPO:0100981', 'abnormal dorsal longitudinal anastomosing vessel', 0.4117647058823529, 5.249153838287537, 1.4701755971154233, 'UPHENO:0080362', 'abnormal cardiovascular system'),
(403450, 'HP:0011599', 'Mesocardia', 'XPO:0101638', 'abnormal anatomical structure morphology', 0.4230769230769231, 2.485033483301678, 1.0253586298746415, 'UPHENO:0076692', 'abnormal anatomical entity morphology'),
(403451, 'HP:0011599', 'Mesocardia', 'XPO:0139990', 'abnormally necrotic cardiovascular system', 0.425, 5.9590888072311134, 1.5914184688739863, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(403452, 'HP:0011599', 'Mesocardia', 'XPO:0139811', 'abnormally necrotic circulatory system', 0.425, 5.9590888072311134, 1.5914184688739863, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(403453, 'HP:0011599', 'Mesocardia', 'XPO:0102532', 'abnormal angioblast morphology', 0.4358974358974359, 5.9590888072311134, 1.6116921329326988, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(403454, 'HP:0011599', 'Mesocardia', 'XPO:0102113', 'abnormal anatomical line morphology', 0.4230769230769231, 2.485033483301678, 1.0253586298746415, 'UPHENO:0076692', 'abnormal anatomical entity morphology'),
(403455, 'HP:0011599', 'Mesocardia', 'XPO:0100076', 'abnormal artery', 0.4117647058823529, 5.249153838287537, 1.4701755971154233, 'UPHENO:0080362', 'abnormal cardiovascular system'),
(403456, 'HP:0011599', 'Mesocardia', 'XPO:0101976', 'abnormal portion of organism substance morphology', 0.4230769230769231, 2.485033483301678, 1.0253586298746415, 'UPHENO:0076692', 'abnormal anatomical entity morphology'),
(403457, 'HP:0011599', 'Mesocardia', 'XPO:0128481', 'decreased size of the circulatory system', 0.40476190476190477, 5.9590888072311134, 1.5530653998657664, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(403458, 'HP:0011599', 'Mesocardia', 'XPO:0129961', 'increased size of the circulatory system', 0.40476190476190477, 5.9590888072311134, 1.5530653998657664, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(403459, 'HP:0011599', 'Mesocardia', 'XPO:0129512', 'increased size of the cardiovascular system', 0.40476190476190477, 5.9590888072311134, 1.5530653998657664, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(403460, 'HP:0011599', 'Mesocardia', 'XPO:0101995', 'abnormal cardiovascular system morphology', 0.5, 5.9590888072311134, 1.7261356851694936, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(403461, 'HP:0011599', 'Mesocardia', 'XPO:0101583', 'abnormal truncus arteriosus', 0.4117647058823529, 5.249153838287537, 1.4701755971154233, 'UPHENO:0080362', 'abnormal cardiovascular system'),
(403462, 'HP:0011599', 'Mesocardia', 'XPO:0100054', 'abnormal blood vessel', 0.42424242424242425, 5.249153838287537, 1.4922847414540332, 'UPHENO:0080362', 'abnormal cardiovascular system'),
(403463, 'HP:0011599', 'Mesocardia', 'XPO:0102935', 'abnormal bulbous arteriosis morphology', 0.4594594594594595, 5.9590888072311134, 1.6546781325204374, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(403464, 'HP:0011599', 'Mesocardia', 'XPO:0101686', 'abnormal blood vessel morphology', 0.40476190476190477, 5.9590888072311134, 1.5530653998657664, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(403465, 'HP:0033630', 'Brain fog', 'XPO:0100175', 'abnormal migrating neuroblast', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(403466, 'HP:0033630', 'Brain fog', 'XPO:0100114', 'abnormal peripheral nervous system', 0.43333333333333335, 3.94131651835137, 1.3068679445984308, 'UPHENO:0004523', 'abnormal nervous system'),
(403467, 'HP:0033630', 'Brain fog', 'XPO:0100004', 'abnormal cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(403468, 'HP:0033630', 'Brain fog', 'XPO:0100158', 'abnormal neuromere', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(403469, 'HP:0033630', 'Brain fog', 'XPO:0100031', 'abnormal central nervous system', 0.4642857142857143, 3.94131651835137, 1.3527368387638634, 'UPHENO:0004523', 'abnormal nervous system'),
(403470, 'HP:0033630', 'Brain fog', 'XPO:0100954', 'abnormal neural progenitor cell', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(403471, 'HP:0033630', 'Brain fog', 'XPO:0100537', 'abnormal medium cavity', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(403472, 'HP:0033630', 'Brain fog', 'XPO:0100642', 'abnormal gustatory system', 0.4482758620689655, 3.94131651835137, 1.3292091859262085, 'UPHENO:0004523', 'abnormal nervous system'),
(403473, 'HP:0033630', 'Brain fog', 'XPO:0100164', 'abnormal neural nucleus', 0.43333333333333335, 3.94131651835137, 1.3068679445984308, 'UPHENO:0004523', 'abnormal nervous system'),
(403474, 'HP:0033630', 'Brain fog', 'XPO:0100734', 'abnormal lateral line system', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(403475, 'HP:0033630', 'Brain fog', 'XPO:0100196', 'abnormal neuron', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(403476, 'HP:0033630', 'Brain fog', 'XPO:0100760', 'abnormal Stirnorgan', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(403477, 'HP:0033630', 'Brain fog', 'XPO:0107253', 'abnormal enteric nervous system', 0.4642857142857143, 3.94131651835137, 1.3527368387638634, 'UPHENO:0004523', 'abnormal nervous system'),
(403478, 'HP:0033630', 'Brain fog', 'XPO:0142051', 'abnormal cerebrospinal fluid', 0.43333333333333335, 3.94131651835137, 1.3068679445984308, 'UPHENO:0004523', 'abnormal nervous system'),
(403479, 'HP:0033630', 'Brain fog', 'XPO:0100864', 'abnormal dorsolateral ascending neuron', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(403480, 'HP:0033630', 'Brain fog', 'XPO:0100702', 'abnormal glial cell', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(403481, 'HP:0033630', 'Brain fog', 'XPO:0100858', 'abnormal presumptive midbrain-hindbrain boundary', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(403482, 'HP:0033630', 'Brain fog', 'XPO:0100701', 'abnormal microglial cell', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(403483, 'HP:0033630', 'Brain fog', 'XPO:0100273', 'abnormal visual system', 0.4482758620689655, 3.94131651835137, 1.3292091859262085, 'UPHENO:0004523', 'abnormal nervous system'),
(403484, 'HP:0033630', 'Brain fog', 'XPO:0100587', 'abnormal vestibuloauditory system', 0.4482758620689655, 3.94131651835137, 1.3292091859262085, 'UPHENO:0004523', 'abnormal nervous system'),
(403485, 'HP:0033630', 'Brain fog', 'XPO:0101133', 'abnormal motor neuron', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(403486, 'HP:0033630', 'Brain fog', 'XPO:0101187', 'abnormal dorsolateral commissural neuron', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(403487, 'HP:0033630', 'Brain fog', 'XPO:0100032', 'abnormal nervous system', 0.48148148148148145, 3.94131651835137, 1.3775597686645948, 'UPHENO:0004523', 'abnormal nervous system'),
(403488, 'HP:0033630', 'Brain fog', 'XPO:0101501', 'abnormal parabrachial area', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(403489, 'HP:0033630', 'Brain fog', 'XPO:0100427', 'abnormal olfactory system', 0.4482758620689655, 3.94131651835137, 1.3292091859262085, 'UPHENO:0004523', 'abnormal nervous system'),
(403490, 'HP:0033630', 'Brain fog', 'XPO:0100274', 'abnormal sensory system', 0.4642857142857143, 3.94131651835137, 1.3527368387638634, 'UPHENO:0004523', 'abnormal nervous system'),
(403491, 'HP:0033630', 'Brain fog', 'XPO:0100916', 'abnormal principal cavity', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(403492, 'HP:0012142', 'Pancreatic squamous cell carcinoma', 'XPO:0126466', 'abnormally localised alimentary system', 0.42857142857142855, 5.05060299610679, 1.471238981671103, 'HP:0025031', 'Abnormality of the digestive system'),
(403493, 'HP:0012142', 'Pancreatic squamous cell carcinoma', 'XPO:0100754', 'abnormal electrically active cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(403494, 'HP:0012142', 'Pancreatic squamous cell carcinoma', 'XPO:0141717', 'abnormal tracheoesophageal fold', 0.45454545454545453, 5.05060299610679, 1.5151662069205463, 'HP:0025031', 'Abnormality of the digestive system'),
(403495, 'HP:0012142', 'Pancreatic squamous cell carcinoma', 'XPO:0101381', 'abnormal ventral foregut', 0.5, 5.05060299610679, 1.5891197242666757, 'HP:0025031', 'Abnormality of the digestive system'),
(403496, 'HP:0012142', 'Pancreatic squamous cell carcinoma', 'XPO:0101448', 'abnormal myelin accumulating cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(403497, 'HP:0012142', 'Pancreatic squamous cell carcinoma', 'XPO:0100591', 'abnormal pharyngeal arch', 0.4411764705882353, 5.05060299610679, 1.4927180591674907, 'HP:0025031', 'Abnormality of the digestive system'),
(403498, 'HP:0012142', 'Pancreatic squamous cell carcinoma', 'XPO:0100893', 'abnormal hyoid arch', 0.42857142857142855, 5.05060299610679, 1.471238981671103, 'HP:0025031', 'Abnormality of the digestive system'),
(403499, 'HP:0012142', 'Pancreatic squamous cell carcinoma', 'XPO:0131683', 'abnormal stomach epithelium', 0.4411764705882353, 5.05060299610679, 1.4927180591674907, 'HP:0025031', 'Abnormality of the digestive system'),
(403500, 'HP:0012142', 'Pancreatic squamous cell carcinoma', 'XPO:0100172', 'abnormal stem cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(403501, 'HP:0012142', 'Pancreatic squamous cell carcinoma', 'XPO:0124857', 'absent alimentary system', 0.4166666666666667, 5.05060299610679, 1.45066119926208, 'HP:0025031', 'Abnormality of the digestive system'),
(403502, 'HP:0012142', 'Pancreatic squamous cell carcinoma', 'XPO:0100903', 'abnormal dorsal pancreatic bud', 0.4166666666666667, 5.05060299610679, 1.45066119926208, 'HP:0025031', 'Abnormality of the digestive system'),
(403503, 'HP:0012142', 'Pancreatic squamous cell carcinoma', 'XPO:0127307', 'abnormally localised oral evagination', 0.40540540540540543, 5.05060299610679, 1.4309233924911664, 'HP:0025031', 'Abnormality of the digestive system'),
(403504, 'HP:0012142', 'Pancreatic squamous cell carcinoma', 'XPO:0100571', 'abnormal branchial arch 1', 0.4166666666666667, 5.05060299610679, 1.45066119926208, 'HP:0025031', 'Abnormality of the digestive system'),
(403505, 'HP:0012142', 'Pancreatic squamous cell carcinoma', 'XPO:0101373', 'abnormal oxygen accumulating cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(403506, 'HP:0012142', 'Pancreatic squamous cell carcinoma', 'XPO:0100454', 'abnormal lung bud', 0.42857142857142855, 5.05060299610679, 1.471238981671103, 'HP:0025031', 'Abnormality of the digestive system'),
(403507, 'HP:0012142', 'Pancreatic squamous cell carcinoma', 'XPO:0101101', 'abnormal posterior foregut', 0.5, 5.05060299610679, 1.5891197242666757, 'HP:0025031', 'Abnormality of the digestive system'),
(403508, 'HP:0012142', 'Pancreatic squamous cell carcinoma', 'XPO:0100608', 'abnormal pancreas', 0.5, 8.724209809801746, 2.088565274273436, 'HP:0001732', 'Abnormality of the pancreas'),
(403509, 'HP:0012142', 'Pancreatic squamous cell carcinoma', 'XPO:0115392', 'abnormally incomplete structure of alimentary system', 0.40540540540540543, 5.05060299610679, 1.4309233924911664, 'HP:0025031', 'Abnormality of the digestive system'),
(403510, 'HP:0012142', 'Pancreatic squamous cell carcinoma', 'XPO:0100344', 'abnormal portion of organism substance', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(403511, 'HP:0012142', 'Pancreatic squamous cell carcinoma', 'XPO:0101004', 'abnormal acid secreting cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(403512, 'HP:0012142', 'Pancreatic squamous cell carcinoma', 'XPO:0141620', 'metaplastic pancreas', 0.46153846153846156, 8.724209809801746, 2.0066286088249243, 'HP:0001732', 'Abnormality of the pancreas'),
(403513, 'HP:0012142', 'Pancreatic squamous cell carcinoma', 'XPO:0100362', 'abnormal acinar cell', 0.45, 8.724209809801746, 1.981386992591499, 'HP:0001732', 'Abnormality of the pancreas'),
(403514, 'HP:0012142', 'Pancreatic squamous cell carcinoma', 'XPO:0101198', 'abnormal digestive enzyme secreting cell', 0.46875, 5.05060299610679, 1.5386585568036393, 'HP:0025031', 'Abnormality of the digestive system'),
(403515, 'HP:0012142', 'Pancreatic squamous cell carcinoma', 'XPO:0100214', 'abnormal second pancreatic bud', 0.45454545454545453, 5.05060299610679, 1.5151662069205463, 'HP:0025031', 'Abnormality of the digestive system'),
(403516, 'HP:0012142', 'Pancreatic squamous cell carcinoma', 'XPO:0100715', 'abnormal ciliated cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(403517, 'HP:0012142', 'Pancreatic squamous cell carcinoma', 'XPO:0100788', 'abnormal branchial arch 4', 0.4166666666666667, 5.05060299610679, 1.45066119926208, 'HP:0025031', 'Abnormality of the digestive system'),
(403518, 'HP:0012142', 'Pancreatic squamous cell carcinoma', 'XPO:0101435', 'abnormal paracrine cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(403519, 'HP:0012142', 'Pancreatic squamous cell carcinoma', 'XPO:0100188', 'abnormal delta cell', 0.42857142857142855, 5.05060299610679, 1.471238981671103, 'HP:0025031', 'Abnormality of the digestive system'),
(403520, 'HP:0012142', 'Pancreatic squamous cell carcinoma', 'XPO:0100852', 'abnormal interdigital region', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(403521, 'HP:0012142', 'Pancreatic squamous cell carcinoma', 'XPO:0126520', 'abnormally localised hindgut', 0.40540540540540543, 5.05060299610679, 1.4309233924911664, 'HP:0025031', 'Abnormality of the digestive system'),
(403522, 'HP:0012142', 'Pancreatic squamous cell carcinoma', 'XPO:0126837', 'abnormally localised midgut', 0.40540540540540543, 5.05060299610679, 1.4309233924911664, 'HP:0025031', 'Abnormality of the digestive system'),
(403523, 'HP:0012142', 'Pancreatic squamous cell carcinoma', 'XPO:0101535', 'abnormal absorptive cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(403524, 'HP:0012142', 'Pancreatic squamous cell carcinoma', 'XPO:0125745', 'absent pharyngeal cavity', 0.4166666666666667, 5.05060299610679, 1.45066119926208, 'HP:0025031', 'Abnormality of the digestive system'),
(403525, 'HP:0012142', 'Pancreatic squamous cell carcinoma', 'XPO:0142054', 'abnormal digestive tract', 0.5357142857142857, 5.05060299610679, 1.6448951870820767, 'HP:0025031', 'Abnormality of the digestive system'),
(403526, 'HP:0012142', 'Pancreatic squamous cell carcinoma', 'XPO:0101084', 'abnormal mesentery', 0.42857142857142855, 5.05060299610679, 1.471238981671103, 'HP:0025031', 'Abnormality of the digestive system'),
(403527, 'HP:0012142', 'Pancreatic squamous cell carcinoma', 'XPO:0100662', 'abnormal lung primordium', 0.40540540540540543, 5.05060299610679, 1.4309233924911664, 'HP:0025031', 'Abnormality of the digestive system'),
(403528, 'HP:0012142', 'Pancreatic squamous cell carcinoma', 'XPO:0124888', 'absent liver and biliary system', 0.40540540540540543, 5.05060299610679, 1.4309233924911664, 'HP:0025031', 'Abnormality of the digestive system'),
(403529, 'HP:0012142', 'Pancreatic squamous cell carcinoma', 'XPO:0100523', 'abnormal midgut', 0.5172413793103449, 5.05060299610679, 1.6162861318637973, 'HP:0025031', 'Abnormality of the digestive system'),
(403530, 'HP:0012142', 'Pancreatic squamous cell carcinoma', 'XPO:0100494', 'abnormal liver diverticulum', 0.42857142857142855, 5.05060299610679, 1.471238981671103, 'HP:0025031', 'Abnormality of the digestive system'),
(403531, 'HP:0012142', 'Pancreatic squamous cell carcinoma', 'XPO:0100718', 'abnormal ventral pancreatic bud', 0.4838709677419355, 5.05060299610679, 1.5632786569919361, 'HP:0025031', 'Abnormality of the digestive system'),
(403532, 'HP:0012142', 'Pancreatic squamous cell carcinoma', 'XPO:0101169', 'abnormal hepato-pancreatic duct', 0.4838709677419355, 5.05060299610679, 1.5632786569919361, 'HP:0025031', 'Abnormality of the digestive system'),
(403533, 'HP:0012142', 'Pancreatic squamous cell carcinoma', 'XPO:0100533', 'abnormal melanoblast', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(403534, 'HP:0012142', 'Pancreatic squamous cell carcinoma', 'XPO:0100572', 'abnormal branchial arch', 0.42857142857142855, 5.05060299610679, 1.471238981671103, 'HP:0025031', 'Abnormality of the digestive system'),
(403535, 'HP:0012142', 'Pancreatic squamous cell carcinoma', 'XPO:0100285', 'abnormal progenitor cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(403536, 'HP:0012142', 'Pancreatic squamous cell carcinoma', 'XPO:0100486', 'abnormal oral evagination', 0.5172413793103449, 5.05060299610679, 1.6162861318637973, 'HP:0025031', 'Abnormality of the digestive system'),
(403537, 'HP:0012142', 'Pancreatic squamous cell carcinoma', 'XPO:0101021', 'abnormal dorsal foregut', 0.5, 5.05060299610679, 1.5891197242666757, 'HP:0025031', 'Abnormality of the digestive system'),
(403538, 'HP:0012142', 'Pancreatic squamous cell carcinoma', 'XPO:0100579', 'abnormal biliary tree', 0.42105263157894735, 7.1173123385767045, 1.731116139930257, 'HP:0002012', 'Abnormality of the abdominal organs'),
(403539, 'HP:0012142', 'Pancreatic squamous cell carcinoma', 'XPO:0100289', 'abnormal chondroblast', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(403540, 'HP:0012142', 'Pancreatic squamous cell carcinoma', 'XPO:0100492', 'abnormal gall bladder primordium', 0.46875, 5.05060299610679, 1.5386585568036393, 'HP:0025031', 'Abnormality of the digestive system'),
(403541, 'HP:0012142', 'Pancreatic squamous cell carcinoma', 'XPO:0107304', 'abnormal hindgut endoderm', 0.46875, 5.05060299610679, 1.5386585568036393, 'HP:0025031', 'Abnormality of the digestive system'),
(403542, 'HP:0012142', 'Pancreatic squamous cell carcinoma', 'XPO:0100130', 'abnormal mouth primordium', 0.4411764705882353, 5.05060299610679, 1.4927180591674907, 'HP:0025031', 'Abnormality of the digestive system'),
(403543, 'HP:0012142', 'Pancreatic squamous cell carcinoma', 'XPO:0100802', 'abnormal exocrine cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(403544, 'HP:0012142', 'Pancreatic squamous cell carcinoma', 'XPO:0100691', 'abnormal keratin accumulating cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(403545, 'HP:0012142', 'Pancreatic squamous cell carcinoma', 'XPO:0100006', 'abnormal anatomical structure', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(403546, 'HP:0012142', 'Pancreatic squamous cell carcinoma', 'XPO:0101103', 'abnormal pharyngeal mesenchyme', 0.42857142857142855, 5.05060299610679, 1.471238981671103, 'HP:0025031', 'Abnormality of the digestive system'),
(403547, 'HP:0012142', 'Pancreatic squamous cell carcinoma', 'XPO:0107288', 'abnormal larval alimentary system', 0.5555555555555556, 5.05060299610679, 1.6750792677938144, 'HP:0025031', 'Abnormality of the digestive system'),
(403548, 'HP:0012142', 'Pancreatic squamous cell carcinoma', 'XPO:0142027', 'abnormally localised digestive tract', 0.40540540540540543, 5.05060299610679, 1.4309233924911664, 'HP:0025031', 'Abnormality of the digestive system'),
(403549, 'HP:0012142', 'Pancreatic squamous cell carcinoma', 'XPO:0101467', 'abnormal alkali secreting cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(403550, 'HP:0012142', 'Pancreatic squamous cell carcinoma', 'XPO:0101784', 'abnormal alimentary system morphology', 0.4166666666666667, 5.05060299610679, 1.45066119926208, 'HP:0025031', 'Abnormality of the digestive system'),
(403551, 'HP:0012142', 'Pancreatic squamous cell carcinoma', 'XPO:0100481', 'abnormal anatomical line', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(403552, 'HP:0012142', 'Pancreatic squamous cell carcinoma', 'XPO:0102522', 'abnormal pharyngeal cavity morphology', 0.4166666666666667, 5.05060299610679, 1.45066119926208, 'HP:0025031', 'Abnormality of the digestive system'),
(403553, 'HP:0012142', 'Pancreatic squamous cell carcinoma', 'XPO:0131673', 'abnormal buccopharyngeal membrane', 0.42857142857142855, 5.05060299610679, 1.471238981671103, 'HP:0025031', 'Abnormality of the digestive system'),
(403554, 'HP:0012142', 'Pancreatic squamous cell carcinoma', 'XPO:0101601', 'abnormal proctodeum', 0.4838709677419355, 5.05060299610679, 1.5632786569919361, 'HP:0025031', 'Abnormality of the digestive system'),
(403555, 'HP:0012142', 'Pancreatic squamous cell carcinoma', 'XPO:0101132', 'abnormal apoptotic cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(403556, 'HP:0012142', 'Pancreatic squamous cell carcinoma', 'XPO:0115391', 'abnormally undifferentiated alimentary system', 0.5555555555555556, 5.05060299610679, 1.6750792677938144, 'HP:0025031', 'Abnormality of the digestive system'),
(403557, 'HP:0012142', 'Pancreatic squamous cell carcinoma', 'XPO:0107307', 'abnormal posterior hindgut endoderm', 0.45454545454545453, 5.05060299610679, 1.5151662069205463, 'HP:0025031', 'Abnormality of the digestive system'),
(403558, 'HP:0012142', 'Pancreatic squamous cell carcinoma', 'XPO:0100890', 'abnormal pharyngeal cavity', 0.5357142857142857, 5.05060299610679, 1.6448951870820767, 'HP:0025031', 'Abnormality of the digestive system'),
(403559, 'HP:0012142', 'Pancreatic squamous cell carcinoma', 'XPO:0115407', 'multiple pancreases', 0.4864864864864865, 8.724209809801746, 2.060148096070132, 'HP:0001732', 'Abnormality of the pancreas'),
(403560, 'HP:0012142', 'Pancreatic squamous cell carcinoma', 'XPO:0100204', 'abnormal islets of Langerhans', 0.45, 8.724209809801746, 1.981386992591499, 'HP:0001732', 'Abnormality of the pancreas'),
(403561, 'HP:0012142', 'Pancreatic squamous cell carcinoma', 'XPO:0126608', 'abnormally localised foregut', 0.40540540540540543, 5.05060299610679, 1.4309233924911664, 'HP:0025031', 'Abnormality of the digestive system'),
(403562, 'HP:0012142', 'Pancreatic squamous cell carcinoma', 'XPO:0100152', 'abnormal alimentary system', 0.5769230769230769, 5.05060299610679, 1.706988406765213, 'HP:0025031', 'Abnormality of the digestive system'),
(403563, 'HP:0012142', 'Pancreatic squamous cell carcinoma', 'XPO:0100735', 'abnormal hindgut', 0.5172413793103449, 5.05060299610679, 1.6162861318637973, 'HP:0025031', 'Abnormality of the digestive system'),
(403564, 'HP:0012142', 'Pancreatic squamous cell carcinoma', 'XPO:0107306', 'abnormal ventral posterior hindgut endoderm', 0.4411764705882353, 5.05060299610679, 1.4927180591674907, 'HP:0025031', 'Abnormality of the digestive system'),
(403565, 'HP:0012142', 'Pancreatic squamous cell carcinoma', 'XPO:0101241', 'abnormal nucleate erythrocyte', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(403566, 'HP:0012142', 'Pancreatic squamous cell carcinoma', 'XPO:0101356', 'abnormal exocrine pancreas', 0.4864864864864865, 8.724209809801746, 2.060148096070132, 'HP:0001732', 'Abnormality of the pancreas'),
(403567, 'HP:0012142', 'Pancreatic squamous cell carcinoma', 'XPO:0115495', 'abnormally protruding proctodeum', 0.4411764705882353, 5.05060299610679, 1.4927180591674907, 'HP:0025031', 'Abnormality of the digestive system'),
(403568, 'HP:0012142', 'Pancreatic squamous cell carcinoma', 'XPO:0100081', 'abnormal anatomical entity in vitro', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(403569, 'HP:0012142', 'Pancreatic squamous cell carcinoma', 'XPO:0101326', 'abnormal cementoblast', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(403570, 'HP:0012142', 'Pancreatic squamous cell carcinoma', 'XPO:0100108', 'abnormal cell part', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(403571, 'HP:0012142', 'Pancreatic squamous cell carcinoma', 'XPO:0126499', 'abnormally localised liver and biliary system', 0.4166666666666667, 5.05060299610679, 1.45066119926208, 'HP:0025031', 'Abnormality of the digestive system'),
(403572, 'HP:0012142', 'Pancreatic squamous cell carcinoma', 'XPO:0100704', 'abnormal Merkel cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(403573, 'HP:0012142', 'Pancreatic squamous cell carcinoma', 'XPO:0127393', 'abnormally localised pharyngeal cavity', 0.42857142857142855, 5.05060299610679, 1.471238981671103, 'HP:0025031', 'Abnormality of the digestive system'),
(403574, 'HP:0012142', 'Pancreatic squamous cell carcinoma', 'XPO:0100621', 'abnormal peritoneum', 0.46875, 5.05060299610679, 1.5386585568036393, 'HP:0025031', 'Abnormality of the digestive system'),
(403575, 'HP:0012142', 'Pancreatic squamous cell carcinoma', 'XPO:0100986', 'abnormal gut epithelium', 0.5, 5.05060299610679, 1.5891197242666757, 'HP:0025031', 'Abnormality of the digestive system'),
(403576, 'HP:0012142', 'Pancreatic squamous cell carcinoma', 'XPO:0100004', 'abnormal cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(403577, 'HP:0012142', 'Pancreatic squamous cell carcinoma', 'XPO:0100629', 'abnormal branchial arch 2', 0.4166666666666667, 5.05060299610679, 1.45066119926208, 'HP:0025031', 'Abnormality of the digestive system'),
(403578, 'HP:0012142', 'Pancreatic squamous cell carcinoma', 'XPO:0100215', 'abnormal first pancreatic bud', 0.46875, 5.05060299610679, 1.5386585568036393, 'HP:0025031', 'Abnormality of the digestive system'),
(403579, 'HP:0012142', 'Pancreatic squamous cell carcinoma', 'XPO:0101193', 'abnormal bile duct', 0.41025641025641024, 7.1173123385767045, 1.7087782216244842, 'HP:0002012', 'Abnormality of the abdominal organs'),
(403580, 'HP:0012142', 'Pancreatic squamous cell carcinoma', 'XPO:0107305', 'abnormal dorsal posterior hindgut endoderm', 0.4411764705882353, 5.05060299610679, 1.4927180591674907, 'HP:0025031', 'Abnormality of the digestive system'),
(403581, 'HP:0012142', 'Pancreatic squamous cell carcinoma', 'XPO:0126705', 'abnormally localised larval alimentary system', 0.40540540540540543, 5.05060299610679, 1.4309233924911664, 'HP:0025031', 'Abnormality of the digestive system'),
(403582, 'HP:0012142', 'Pancreatic squamous cell carcinoma', 'XPO:0100026', 'abnormal germ cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(403583, 'HP:0012142', 'Pancreatic squamous cell carcinoma', 'XPO:0100216', 'abnormal hepato-pancreatic progenitor cell', 0.4411764705882353, 5.05060299610679, 1.4927180591674907, 'HP:0025031', 'Abnormality of the digestive system'),
(403584, 'HP:0012142', 'Pancreatic squamous cell carcinoma', 'XPO:0100653', 'abnormal myoblast', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(403585, 'HP:0012142', 'Pancreatic squamous cell carcinoma', 'XPO:0101333', 'abnormal barrier epithelial cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(403586, 'HP:0012142', 'Pancreatic squamous cell carcinoma', 'XPO:0100493', 'abnormal liver and biliary system', 0.5555555555555556, 5.05060299610679, 1.6750792677938144, 'HP:0025031', 'Abnormality of the digestive system'),
(403587, 'HP:0012142', 'Pancreatic squamous cell carcinoma', 'XPO:0100549', 'abnormal mitotic cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(403588, 'HP:0012142', 'Pancreatic squamous cell carcinoma', 'XPO:0100791', 'abnormal multiciliated cell precursor', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(403589, 'HP:0012142', 'Pancreatic squamous cell carcinoma', 'XPO:0100462', 'abnormal anterior foregut', 0.5, 5.05060299610679, 1.5891197242666757, 'HP:0025031', 'Abnormality of the digestive system'),
(403590, 'HP:0012142', 'Pancreatic squamous cell carcinoma', 'XPO:0100813', 'abnormal branchial arch 3', 0.4166666666666667, 5.05060299610679, 1.45066119926208, 'HP:0025031', 'Abnormality of the digestive system'),
(403591, 'HP:0012142', 'Pancreatic squamous cell carcinoma', 'XPO:0101377', 'abnormal manicotto glandulare', 0.5172413793103449, 5.05060299610679, 1.6162861318637973, 'HP:0025031', 'Abnormality of the digestive system'),
(403592, 'HP:0012142', 'Pancreatic squamous cell carcinoma', 'XPO:0101297', 'abnormal barrier cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(403593, 'HP:0012142', 'Pancreatic squamous cell carcinoma', 'XPO:0100797', 'abnormal esophagus', 0.4166666666666667, 5.05060299610679, 1.45066119926208, 'HP:0025031', 'Abnormality of the digestive system'),
(403594, 'HP:0012142', 'Pancreatic squamous cell carcinoma', 'XPO:0131662', 'abnormal foregut epithelium', 0.4411764705882353, 5.05060299610679, 1.4927180591674907, 'HP:0025031', 'Abnormality of the digestive system'),
(403595, 'HP:0012142', 'Pancreatic squamous cell carcinoma', 'XPO:0101237', 'abnormal mucus secreting cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(403596, 'HP:0012142', 'Pancreatic squamous cell carcinoma', 'XPO:0100638', 'abnormal polar body', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(403597, 'HP:0012142', 'Pancreatic squamous cell carcinoma', 'XPO:0107308', 'abnormal anterior hindgut endoderm', 0.45454545454545453, 5.05060299610679, 1.5151662069205463, 'HP:0025031', 'Abnormality of the digestive system'),
(403598, 'HP:0012142', 'Pancreatic squamous cell carcinoma', 'XPO:0100156', 'abnormal foregut', 0.5172413793103449, 5.05060299610679, 1.6162861318637973, 'HP:0025031', 'Abnormality of the digestive system'),
(403599, 'HP:0012142', 'Pancreatic squamous cell carcinoma', 'XPO:0100477', 'abnormal pericyte', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(403600, 'HP:0012142', 'Pancreatic squamous cell carcinoma', 'XPO:0100337', 'abnormal zygote', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(403601, 'HP:0005321', 'Mandibulofacial dysostosis', 'XPO:0129771', 'increased size of the dermatocranium', 0.41935483870967744, 4.638757693672553, 1.394734915474381, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(403602, 'HP:0005321', 'Mandibulofacial dysostosis', 'XPO:0139784', 'abnormally necrotic cranium', 0.45614035087719296, 4.638757693672553, 1.4546217934659431, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(403603, 'HP:0005321', 'Mandibulofacial dysostosis', 'XPO:0141185', 'abnormally necrotic occipital region', 0.5254237288135594, 7.024697770424301, 1.9211826816637279, 'HP:0000929', 'Abnormal skull morphology'),
(403604, 'HP:0005321', 'Mandibulofacial dysostosis', 'XPO:0102921', 'abnormal orbital region morphology', 0.55, 7.024697770424301, 1.9656001052435275, 'HP:0000929', 'Abnormal skull morphology'),
(403605, 'HP:0005321', 'Mandibulofacial dysostosis', 'XPO:0141835', 'edematous head', 0.4375, 4.5318002188002176, 1.4080705222839853, 'UPHENO:0087907', 'abnormal head morphology'),
(403606, 'HP:0005321', 'Mandibulofacial dysostosis', 'XPO:0101634', 'abnormal head morphology', 0.45652173913043476, 4.5318002188002176, 1.4383550734357495, 'UPHENO:0087907', 'abnormal head morphology'),
(403607, 'HP:0005321', 'Mandibulofacial dysostosis', 'XPO:0130138', 'increased size of the braincase and otic capsule skeleton', 0.40625, 4.638757693672553, 1.3727692133255593, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(403608, 'HP:0005321', 'Mandibulofacial dysostosis', 'XPO:0128668', 'decreased size of the fenestra basicranialis', 0.4482758620689655, 4.638757693672553, 1.4420274283314136, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(403609, 'HP:0005321', 'Mandibulofacial dysostosis', 'XPO:0141339', 'decreased pigmentation in the head', 0.42857142857142855, 4.5318002188002176, 1.3936283915633758, 'UPHENO:0087907', 'abnormal head morphology'),
(403610, 'HP:0005321', 'Mandibulofacial dysostosis', 'XPO:0140560', 'abnormally necrotic orbital region', 0.5076923076923077, 7.024697770424301, 1.8884874958303859, 'HP:0000929', 'Abnormal skull morphology'),
(403611, 'HP:0005321', 'Mandibulofacial dysostosis', 'XPO:0102804', 'abnormal pharyngeal pouch morphology', 0.42857142857142855, 4.5318002188002176, 1.3936283915633758, 'UPHENO:0087907', 'abnormal head morphology'),
(403612, 'HP:0005321', 'Mandibulofacial dysostosis', 'XPO:0140335', 'abnormally necrotic pharyngeal region', 0.4375, 4.5318002188002176, 1.4080705222839853, 'UPHENO:0087907', 'abnormal head morphology'),
(403613, 'HP:0005321', 'Mandibulofacial dysostosis', 'XPO:0128659', 'decreased size of the braincase and otic capsule skeleton', 0.40625, 4.638757693672553, 1.3727692133255593, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(403614, 'HP:0005321', 'Mandibulofacial dysostosis', 'XPO:0140132', 'abnormally necrotic ethmoid region', 0.4482758620689655, 4.638757693672553, 1.4420274283314136, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(403615, 'HP:0005321', 'Mandibulofacial dysostosis', 'XPO:0102005', 'abnormal splanchnocranium morphology', 0.48148148148148145, 4.638757693672553, 1.4944818254442178, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(403616, 'HP:0005321', 'Mandibulofacial dysostosis', 'XPO:0101681', 'abnormal chondrocranium morphology', 0.48148148148148145, 4.638757693672553, 1.4944818254442178, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(403617, 'HP:0005321', 'Mandibulofacial dysostosis', 'XPO:0103381', 'increased size of the head', 0.5344827586206896, 7.024697770424301, 1.9376738226061134, 'HP:0000929', 'Abnormal skull morphology'),
(403618, 'HP:0005321', 'Mandibulofacial dysostosis', 'XPO:0128477', 'decreased size of the neurocranium', 0.49206349206349204, 7.024697770424301, 1.8591926515575539, 'HP:0000929', 'Abnormal skull morphology'),
(403619, 'HP:0005321', 'Mandibulofacial dysostosis', 'XPO:0129406', 'decreased size of the suspensorium', 0.4262295081967213, 4.638757693672553, 1.4061206955371255, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(403620, 'HP:0005321', 'Mandibulofacial dysostosis', 'XPO:0103707', 'increased pigmentation in the head', 0.42857142857142855, 4.5318002188002176, 1.3936283915633758, 'UPHENO:0087907', 'abnormal head morphology'),
(403621, 'HP:0005321', 'Mandibulofacial dysostosis', 'XPO:0128033', 'decreased size of the splanchnocranium', 0.41935483870967744, 4.638757693672553, 1.394734915474381, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(403622, 'HP:0005321', 'Mandibulofacial dysostosis', 'XPO:0130147', 'increased size of the fenestra basicranialis', 0.4482758620689655, 4.638757693672553, 1.4420274283314136, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(403623, 'HP:0005321', 'Mandibulofacial dysostosis', 'XPO:0129225', 'decreased size of the upper jaw', 0.4342105263157895, 7.024697770424301, 1.7464815246962357, 'HP:0000929', 'Abnormal skull morphology'),
(403624, 'HP:0005321', 'Mandibulofacial dysostosis', 'XPO:0129291', 'decreased size of the orbital region', 0.4782608695652174, 7.024697770424301, 1.832931549217256, 'HP:0000929', 'Abnormal skull morphology'),
(403625, 'HP:0005321', 'Mandibulofacial dysostosis', 'XPO:0102828', 'abnormal occipital region morphology', 0.5740740740740741, 7.024697770424301, 2.008157580521644, 'HP:0000929', 'Abnormal skull morphology'),
(403626, 'HP:0005321', 'Mandibulofacial dysostosis', 'XPO:0130425', 'increased size of the otic region', 0.5, 7.024697770424301, 1.8741261657669024, 'HP:0000929', 'Abnormal skull morphology'),
(403627, 'HP:0005321', 'Mandibulofacial dysostosis', 'XPO:0102010', 'abnormal perichondrium morphology', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(403628, 'HP:0005321', 'Mandibulofacial dysostosis', 'XPO:0130383', 'increased size of the occipital region', 0.5081967213114754, 7.024697770424301, 1.8894254087244782, 'HP:0000929', 'Abnormal skull morphology'),
(403629, 'HP:0005321', 'Mandibulofacial dysostosis', 'XPO:0103332', 'decreased size of the chondrocranium', 0.41935483870967744, 4.638757693672553, 1.394734915474381, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(403630, 'HP:0005321', 'Mandibulofacial dysostosis', 'XPO:0102795', 'abnormal branchial basket morphology', 0.40625, 4.638757693672553, 1.3727692133255593, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(403631, 'HP:0005321', 'Mandibulofacial dysostosis', 'XPO:0128291', 'decreased size of the dermatocranium', 0.41935483870967744, 4.638757693672553, 1.394734915474381, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(403632, 'HP:0005321', 'Mandibulofacial dysostosis', 'XPO:0140223', 'abnormally necrotic head region', 0.4117647058823529, 4.5318002188002176, 1.3660290568695288, 'UPHENO:0087907', 'abnormal head morphology'),
(403633, 'HP:0005321', 'Mandibulofacial dysostosis', 'XPO:0129689', 'increased size of the sphenoid region', 0.5, 7.024697770424301, 1.8741261657669024, 'HP:0000929', 'Abnormal skull morphology'),
(403634, 'HP:0005321', 'Mandibulofacial dysostosis', 'XPO:0103152', 'abnormal otic region morphology', 0.5636363636363636, 7.024697770424301, 1.9898178577363366, 'HP:0000929', 'Abnormal skull morphology'),
(403635, 'HP:0005321', 'Mandibulofacial dysostosis', 'XPO:0128905', 'decreased size of the occipital region', 0.5081967213114754, 7.024697770424301, 1.8894254087244782, 'HP:0000929', 'Abnormal skull morphology'),
(403636, 'HP:0005321', 'Mandibulofacial dysostosis', 'XPO:0128846', 'decreased size of the choana', 0.515625, 7.024697770424301, 1.9031841182279317, 'HP:0000929', 'Abnormal skull morphology'),
(403637, 'HP:0005321', 'Mandibulofacial dysostosis', 'XPO:0141061', 'abnormally necrotic suspensorium', 0.4406779661016949, 4.638757693672553, 1.4297546312868548, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(403638, 'HP:0005321', 'Mandibulofacial dysostosis', 'XPO:0139880', 'abnormally necrotic dermatocranium', 0.43333333333333335, 4.638757693672553, 1.4177899470389728, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(403639, 'HP:0005321', 'Mandibulofacial dysostosis', 'XPO:0102572', 'abnormal hatching gland primordium morphology', 0.4117647058823529, 4.5318002188002176, 1.3660290568695288, 'UPHENO:0087907', 'abnormal head morphology'),
(403640, 'HP:0005321', 'Mandibulofacial dysostosis', 'XPO:0128971', 'decreased size of the fenestra subocularis', 0.4482758620689655, 4.638757693672553, 1.4420274283314136, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(403641, 'HP:0005321', 'Mandibulofacial dysostosis', 'XPO:0102351', 'abnormal sphenoid region morphology', 0.5636363636363636, 7.024697770424301, 1.9898178577363366, 'HP:0000929', 'Abnormal skull morphology'),
(403642, 'HP:0005321', 'Mandibulofacial dysostosis', 'XPO:0102217', 'abnormal elastica externa morphology', 0.43478260869565216, 4.638757693672553, 1.4201588541997616, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(403643, 'HP:0005321', 'Mandibulofacial dysostosis', 'XPO:0128034', 'decreased size of the cranium', 0.4406779661016949, 4.638757693672553, 1.4297546312868548, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(403644, 'HP:0005321', 'Mandibulofacial dysostosis', 'XPO:0141829', 'increased width of head', 0.5, 7.024697770424301, 1.8741261657669024, 'HP:0000929', 'Abnormal skull morphology'),
(403645, 'HP:0005321', 'Mandibulofacial dysostosis', 'XPO:0130880', 'increased size of the suspensorium', 0.4262295081967213, 4.638757693672553, 1.4061206955371255, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(403646, 'HP:0005321', 'Mandibulofacial dysostosis', 'XPO:0140926', 'abnormally necrotic neurocranium', 0.5166666666666667, 7.024697770424301, 1.9051055564944135, 'HP:0000929', 'Abnormal skull morphology'),
(403647, 'HP:0005321', 'Mandibulofacial dysostosis', 'XPO:0130358', 'increased size of the lower jaw', 0.44594594594594594, 7.024697770424301, 1.769925278709879, 'HP:0000929', 'Abnormal skull morphology'),
(403648, 'HP:0005321', 'Mandibulofacial dysostosis', 'XPO:0128947', 'decreased size of the otic region', 0.5, 7.024697770424301, 1.8741261657669024, 'HP:0000929', 'Abnormal skull morphology'),
(403649, 'HP:0005321', 'Mandibulofacial dysostosis', 'XPO:0128208', 'decreased size of the olfactory region', 0.5, 7.024697770424301, 1.8741261657669024, 'HP:0000929', 'Abnormal skull morphology'),
(403650, 'HP:0005321', 'Mandibulofacial dysostosis', 'XPO:0102567', 'abnormal skeleton morphology', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(403651, 'HP:0005321', 'Mandibulofacial dysostosis', 'XPO:0128238', 'decreased size of the ethmoid region', 0.43333333333333335, 4.638757693672553, 1.4177899470389728, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(403652, 'HP:0005321', 'Mandibulofacial dysostosis', 'XPO:0141298', 'abnormal intercanthal region morphology', 0.4375, 4.5318002188002176, 1.4080705222839853, 'UPHENO:0087907', 'abnormal head morphology'),
(403653, 'HP:0005321', 'Mandibulofacial dysostosis', 'XPO:0101764', 'abnormal cranium morphology', 0.5, 4.638757693672553, 1.5229507040072823, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(403654, 'HP:0005321', 'Mandibulofacial dysostosis', 'XPO:0102538', 'abnormal lateral nasal prominence morphology', 0.42857142857142855, 4.5318002188002176, 1.3936283915633758, 'UPHENO:0087907', 'abnormal head morphology'),
(403655, 'HP:0005321', 'Mandibulofacial dysostosis', 'XPO:0141839', 'edematous pharyngeal region', 0.44680851063829785, 4.5318002188002176, 1.422971154406314, 'UPHENO:0087907', 'abnormal head morphology'),
(403656, 'HP:0005321', 'Mandibulofacial dysostosis', 'XPO:0129514', 'increased size of the cranium', 0.4406779661016949, 4.638757693672553, 1.4297546312868548, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(403657, 'HP:0005321', 'Mandibulofacial dysostosis', 'XPO:0102082', 'abnormal circumpharyngeal ridge morphology', 0.42, 4.5318002188002176, 1.3796217205799897, 'UPHENO:0087907', 'abnormal head morphology'),
(403658, 'HP:0005321', 'Mandibulofacial dysostosis', 'XPO:0100226', 'abnormal vertebral element', 0.4107142857142857, 6.272837960958401, 1.6050994245019483, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(403659, 'HP:0005321', 'Mandibulofacial dysostosis', 'XPO:0130701', 'increased size of the upper jaw', 0.4342105263157895, 7.024697770424301, 1.7464815246962357, 'HP:0000929', 'Abnormal skull morphology'),
(403660, 'HP:0005321', 'Mandibulofacial dysostosis', 'XPO:0102054', 'abnormal notochord morphology', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(403661, 'HP:0005321', 'Mandibulofacial dysostosis', 'XPO:0102665', 'abnormal suspensorium morphology', 0.48148148148148145, 4.638757693672553, 1.4944818254442178, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(403662, 'HP:0005321', 'Mandibulofacial dysostosis', 'XPO:0142059', 'abnormal nasal region morphology', 0.44680851063829785, 4.5318002188002176, 1.422971154406314, 'UPHENO:0087907', 'abnormal head morphology'),
(403663, 'HP:0005321', 'Mandibulofacial dysostosis', 'XPO:0101860', 'abnormal skeletal subdivision morphology', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(403664, 'HP:0005321', 'Mandibulofacial dysostosis', 'XPO:0102144', 'abnormal cranial skeleton morphology', 0.40384615384615385, 6.211345574613551, 1.5838017617482976, 'UPHENO:0087089', 'abnormal axial skeleton plus cranial skeleton morphology'),
(403665, 'HP:0005321', 'Mandibulofacial dysostosis', 'XPO:0102215', 'abnormal mandibular arch skeleton morphology', 0.45614035087719296, 4.638757693672553, 1.4546217934659431, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(403666, 'HP:0005321', 'Mandibulofacial dysostosis', 'XPO:0102734', 'abnormal craniofacial region morphology', 0.42857142857142855, 4.5318002188002176, 1.3936283915633758, 'UPHENO:0087907', 'abnormal head morphology'),
(403667, 'HP:0005321', 'Mandibulofacial dysostosis', 'XPO:0139775', 'abnormally necrotic braincase and otic capsule skeleton', 0.41935483870967744, 4.638757693672553, 1.394734915474381, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(403668, 'HP:0005321', 'Mandibulofacial dysostosis', 'XPO:0102097', 'abnormal skeletal system morphology', 0.43478260869565216, 4.638757693672553, 1.4201588541997616, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(403669, 'HP:0005321', 'Mandibulofacial dysostosis', 'XPO:0100693', 'abnormal vertebral centrum', 0.40350877192982454, 6.272837960958401, 1.5909573036826314, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(403670, 'HP:0005321', 'Mandibulofacial dysostosis', 'XPO:0100420', 'abnormal choana', 0.5, 5.0624614801082695, 1.590984204841184, 'UPHENO:0002910', 'abnormal face'),
(403671, 'HP:0005321', 'Mandibulofacial dysostosis', 'XPO:0102259', 'abnormal pharyngeal region morphology', 0.4666666666666667, 4.5318002188002176, 1.4542489821577214, 'UPHENO:0087907', 'abnormal head morphology'),
(403672, 'HP:0005321', 'Mandibulofacial dysostosis', 'XPO:0130324', 'increased size of the choana', 0.515625, 7.024697770424301, 1.9031841182279317, 'HP:0000929', 'Abnormal skull morphology'),
(403673, 'HP:0005321', 'Mandibulofacial dysostosis', 'XPO:0128880', 'decreased size of the lower jaw', 0.44594594594594594, 7.024697770424301, 1.769925278709879, 'HP:0000929', 'Abnormal skull morphology'),
(403674, 'HP:0005321', 'Mandibulofacial dysostosis', 'XPO:0129718', 'increased size of the ethmoid region', 0.43333333333333335, 4.638757693672553, 1.4177899470389728, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(403675, 'HP:0005321', 'Mandibulofacial dysostosis', 'XPO:0140914', 'abnormally necrotic intercanthal region', 0.4117647058823529, 4.5318002188002176, 1.3660290568695288, 'UPHENO:0087907', 'abnormal head morphology'),
(403676, 'HP:0005321', 'Mandibulofacial dysostosis', 'XPO:0140639', 'abnormally necrotic upper jaw', 0.44594594594594594, 7.024697770424301, 1.769925278709879, 'HP:0000929', 'Abnormal skull morphology'),
(403677, 'HP:0005321', 'Mandibulofacial dysostosis', 'XPO:0129957', 'increased size of the neurocranium', 0.49206349206349204, 7.024697770424301, 1.8591926515575539, 'HP:0000929', 'Abnormal skull morphology'),
(403678, 'HP:0005321', 'Mandibulofacial dysostosis', 'XPO:0102461', 'abnormal postcranial axial skeleton morphology', 0.4423076923076923, 6.272837960958401, 1.6656903922192745, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(403679, 'HP:0005321', 'Mandibulofacial dysostosis', 'XPO:0103138', 'abnormal upper jaw morphology', 0.4782608695652174, 7.024697770424301, 1.832931549217256, 'HP:0000929', 'Abnormal skull morphology'),
(403680, 'HP:0005321', 'Mandibulofacial dysostosis', 'XPO:0126871', 'abnormally localised choana', 0.4406779661016949, 5.0624614801082695, 1.493624862046119, 'UPHENO:0002910', 'abnormal face'),
(403681, 'HP:0005321', 'Mandibulofacial dysostosis', 'XPO:0103358', 'decreased size of the pharyngeal region', 0.42, 4.5318002188002176, 1.3796217205799897, 'UPHENO:0087907', 'abnormal head morphology'),
(403682, 'HP:0005321', 'Mandibulofacial dysostosis', 'XPO:0115586', 'abnormally decreased volume of chondrocranium', 0.40625, 4.638757693672553, 1.3727692133255593, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(403683, 'HP:0005321', 'Mandibulofacial dysostosis', 'XPO:0140644', 'abnormally necrotic otic region', 0.5166666666666667, 7.024697770424301, 1.9051055564944135, 'HP:0000929', 'Abnormal skull morphology'),
(403684, 'HP:0005321', 'Mandibulofacial dysostosis', 'XPO:0102806', 'abnormal articular system morphology', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(403685, 'HP:0005321', 'Mandibulofacial dysostosis', 'XPO:0115526', 'abnormally incomplete structure of head', 0.44680851063829785, 4.5318002188002176, 1.422971154406314, 'UPHENO:0087907', 'abnormal head morphology'),
(403686, 'HP:0005321', 'Mandibulofacial dysostosis', 'XPO:0129688', 'increased size of the olfactory region', 0.5, 7.024697770424301, 1.8741261657669024, 'HP:0000929', 'Abnormal skull morphology'),
(403687, 'HP:0005321', 'Mandibulofacial dysostosis', 'XPO:0101659', 'abnormal lower jaw morphology', 0.4925373134328358, 7.024697770424301, 1.860087569853209, 'HP:0000929', 'Abnormal skull morphology'),
(403688, 'HP:0005321', 'Mandibulofacial dysostosis', 'XPO:0140672', 'abnormally necrotic olfactory region', 0.5166666666666667, 7.024697770424301, 1.9051055564944135, 'HP:0000929', 'Abnormal skull morphology'),
(403689, 'HP:0005321', 'Mandibulofacial dysostosis', 'XPO:0102052', 'abnormal choana morphology', 0.5689655172413793, 7.024697770424301, 1.9992025411182897, 'HP:0000929', 'Abnormal skull morphology'),
(403690, 'HP:0005321', 'Mandibulofacial dysostosis', 'XPO:0141719', 'abnormal anterior notochord morphology', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(403691, 'HP:0005321', 'Mandibulofacial dysostosis', 'XPO:0139715', 'abnormally necrotic head', 0.4117647058823529, 4.5318002188002176, 1.3660290568695288, 'UPHENO:0087907', 'abnormal head morphology'),
(403692, 'HP:0005321', 'Mandibulofacial dysostosis', 'XPO:0103101', 'abnormal medial nasal prominence morphology', 0.42857142857142855, 4.5318002188002176, 1.3936283915633758, 'UPHENO:0087907', 'abnormal head morphology'),
(403693, 'HP:0005321', 'Mandibulofacial dysostosis', 'XPO:0103176', 'abnormal fenestra basicranialis morphology', 0.49056603773584906, 4.638757693672553, 1.508514826510376, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(403694, 'HP:0005321', 'Mandibulofacial dysostosis', 'XPO:0130767', 'increased size of the orbital region', 0.4782608695652174, 7.024697770424301, 1.832931549217256, 'HP:0000929', 'Abnormal skull morphology'),
(403695, 'HP:0005321', 'Mandibulofacial dysostosis', 'XPO:0128209', 'decreased size of the sphenoid region', 0.5, 7.024697770424301, 1.8741261657669024, 'HP:0000929', 'Abnormal skull morphology'),
(403696, 'HP:0005321', 'Mandibulofacial dysostosis', 'XPO:0102216', 'abnormal vertebral column morphology', 0.4107142857142857, 6.272837960958401, 1.6050994245019483, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(403697, 'HP:0005321', 'Mandibulofacial dysostosis', 'XPO:0141201', 'abnormally necrotic sphenoid region', 0.5166666666666667, 7.024697770424301, 1.9051055564944135, 'HP:0000929', 'Abnormal skull morphology'),
(403698, 'HP:0005321', 'Mandibulofacial dysostosis', 'XPO:0140897', 'abnormally necrotic lower jaw', 0.4583333333333333, 7.024697770424301, 1.7943391944606808, 'HP:0000929', 'Abnormal skull morphology'),
(403699, 'HP:0005321', 'Mandibulofacial dysostosis', 'XPO:0101997', 'abnormal braincase and otic capsule skeleton morphology', 0.4642857142857143, 4.638757693672553, 1.4675520192501232, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(403700, 'HP:0005321', 'Mandibulofacial dysostosis', 'XPO:0102485', 'abnormal osseous labyrinth morphology', 0.41333333333333333, 7.024697770424301, 1.7039782114536297, 'HP:0000929', 'Abnormal skull morphology'),
(403701, 'HP:0005321', 'Mandibulofacial dysostosis', 'XPO:0102564', 'abnormal olfactory region morphology', 0.5636363636363636, 7.024697770424301, 1.9898178577363366, 'HP:0000929', 'Abnormal skull morphology'),
(403702, 'HP:0005321', 'Mandibulofacial dysostosis', 'XPO:0103721', 'increased size of the chondrocranium', 0.41935483870967744, 4.638757693672553, 1.394734915474381, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(403703, 'HP:0005321', 'Mandibulofacial dysostosis', 'XPO:0102092', 'abnormal ethmoid region morphology', 0.49056603773584906, 4.638757693672553, 1.508514826510376, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(403704, 'HP:0005321', 'Mandibulofacial dysostosis', 'XPO:0103739', 'increased size of the pharyngeal region', 0.42, 4.5318002188002176, 1.3796217205799897, 'UPHENO:0087907', 'abnormal head morphology'),
(403705, 'HP:0005321', 'Mandibulofacial dysostosis', 'XPO:0130449', 'increased size of the fenestra subocularis', 0.4482758620689655, 4.638757693672553, 1.4420274283314136, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(403706, 'HP:0005321', 'Mandibulofacial dysostosis', 'XPO:0139832', 'abnormally necrotic splanchnocranium', 0.43333333333333335, 4.638757693672553, 1.4177899470389728, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(403707, 'HP:0005321', 'Mandibulofacial dysostosis', 'XPO:0100584', 'abnormal vertebral column', 0.46, 6.272837960958401, 1.69867756270602, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(403708, 'HP:0005321', 'Mandibulofacial dysostosis', 'XPO:0102776', 'abnormal fenestra subocularis morphology', 0.49056603773584906, 4.638757693672553, 1.508514826510376, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(403709, 'HP:0005321', 'Mandibulofacial dysostosis', 'XPO:0129513', 'increased size of the splanchnocranium', 0.41935483870967744, 4.638757693672553, 1.394734915474381, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(403710, 'HP:0005321', 'Mandibulofacial dysostosis', 'XPO:0125246', 'absent choana', 0.40625, 5.0624614801082695, 1.434093782252048, 'UPHENO:0002910', 'abnormal face'),
(403711, 'HP:0005321', 'Mandibulofacial dysostosis', 'XPO:0101483', 'abnormal nostril', 0.4339622641509434, 5.0624614801082695, 1.482200136987148, 'UPHENO:0002910', 'abnormal face'),
(403712, 'HP:0005321', 'Mandibulofacial dysostosis', 'XPO:0141193', 'abnormally necrotic mandibular arch skeleton', 0.4126984126984127, 4.638757693672553, 1.3836213127410304, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(403713, 'HP:0005321', 'Mandibulofacial dysostosis', 'XPO:0102720', 'abnormal dermatocranium morphology', 0.48148148148148145, 4.638757693672553, 1.4944818254442178, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(403714, 'HP:0005321', 'Mandibulofacial dysostosis', 'XPO:0141723', 'abnormal posterior notochord morphology', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(403715, 'HP:0005321', 'Mandibulofacial dysostosis', 'XPO:0102401', 'abnormal neurocranium morphology', 0.5636363636363636, 7.024697770424301, 1.9898178577363366, 'HP:0000929', 'Abnormal skull morphology'),
(403716, 'HP:0005321', 'Mandibulofacial dysostosis', 'XPO:0107372', 'abnormal flexural organ morphology', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(403717, 'HP:0005321', 'Mandibulofacial dysostosis', 'XPO:0102272', 'abnormal notochordal sheath morphology', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(403718, 'HP:0005321', 'Mandibulofacial dysostosis', 'XPO:0139745', 'abnormally necrotic chondrocranium', 0.43333333333333335, 4.638757693672553, 1.4177899470389728, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(403719, 'HP:0005321', 'Mandibulofacial dysostosis', 'XPO:0101957', 'abnormal axial skeleton morphology', 0.4117647058823529, 6.211345574613551, 1.599253852164941, 'UPHENO:0087089', 'abnormal axial skeleton plus cranial skeleton morphology'),
(403720, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0100258', 'abnormal organ part', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(403721, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0101221', 'abnormal larval immune system', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(403722, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0141792', 'abnormal small molecule metabolic process', 0.5238095238095238, 4.758907843651163, 1.5788480773767701, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(403723, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0131469', 'abnormal heart process', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(403724, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0107284', 'abnormal migrating myoblast', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(403725, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0100852', 'abnormal interdigital region', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(403726, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0100549', 'abnormal mitotic cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(403727, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0100969', 'abnormal disaggregated/reaggregated ectoderm treated with activin', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(403728, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0100626', 'abnormal primordial germ cell', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(403729, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0141910', 'abnormal D-ribose metabolic process', 0.4230769230769231, 4.758907843651163, 1.418937661667548, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(403730, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0100754', 'abnormal electrically active cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(403731, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0100894', 'abnormal nucleus', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(403732, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0107260', 'abnormal anterior-posterior axis', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(403733, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0116434', 'abnormal biological process', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(403734, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0101333', 'abnormal barrier epithelial cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(403735, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0141854', 'abnormal glutathione metabolic process', 0.4230769230769231, 4.758907843651163, 1.418937661667548, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(403736, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0101110', 'abnormal cell-free extract', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(403737, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0100239', 'abnormal acellular anatomical structure', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(403738, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0133403', 'abnormal developmental process', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(403739, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0141770', 'abnormal urate homeostasis', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(403740, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0101472', 'abnormal zygote cortex', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(403741, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0141272', 'absent surface breathing', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(403742, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0100691', 'abnormal keratin accumulating cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(403743, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0101467', 'abnormal alkali secreting cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(403744, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0100172', 'abnormal stem cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(403745, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0101373', 'abnormal oxygen accumulating cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(403746, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0101461', 'abnormal sperm entry point', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(403747, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0131677', 'abnormal actin filament', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(403748, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0101297', 'abnormal barrier cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(403749, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0141796', 'abnormal demethylation', 0.5238095238095238, 4.758907843651163, 1.5788480773767701, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(403750, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0131723', 'abnormal pathway-restricted SMAD protein phosphorylation', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(403751, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0131691', 'abnormal molecular function', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(403752, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0141884', 'abnormal phosphagen metabolic process', 0.4230769230769231, 4.758907843651163, 1.418937661667548, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(403753, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0100481', 'abnormal anatomical line', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(403754, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0141777', 'abnormal catabolic process', 0.5238095238095238, 4.758907843651163, 1.5788480773767701, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(403755, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0141600', 'absent metamorphosis', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(403756, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0141859', 'abnormal lactose catabolic process', 0.4230769230769231, 4.758907843651163, 1.418937661667548, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(403757, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0100344', 'abnormal portion of organism substance', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(403758, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0131667', 'abnormal actin cytoskeleton', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(403759, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0100724', 'abnormal kinetochore', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(403760, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0100956', 'abnormal centrosome', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(403761, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0100010', 'abnormal multicellular anatomical structure', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(403762, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0100907', 'abnormal cytoplasm', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(403763, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0100437', 'abnormal proepicardium', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(403764, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0100653', 'abnormal myoblast', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(403765, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0141787', 'abnormal hormone metabolic process', 0.5238095238095238, 4.758907843651163, 1.5788480773767701, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(403766, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0100372', 'abnormal hematological system', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(403767, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0107253', 'abnormal enteric nervous system', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(403768, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0100976', 'abnormal multiciliated cell', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(403769, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0141866', 'abnormal dicarboxylic acid metabolic process', 0.4074074074074074, 4.758907843651163, 1.392413123563799, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(403770, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:00000000', 'Xenopus phenotype', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(403771, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0100006', 'abnormal anatomical structure', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(403772, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0141864', 'abnormal 5-methylcytosine metabolic process', 0.4230769230769231, 4.758907843651163, 1.418937661667548, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(403773, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0141767', 'abnormal temperature homeostasis', 0.44, 4.758907843651163, 1.447038165082909, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(403774, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0100721', 'abnormal centromere', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(403775, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0141267', 'abnormal resting posture', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(403776, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0100386', 'abnormal limb', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(403777, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0100728', 'abnormal cell condensation', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(403778, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0141790', 'abnormal cellular metabolic process', 0.5, 4.758907843651163, 1.5425478669479211, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(403779, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0100917', 'abnormal stage III oocyte', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(403780, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0100599', 'abnormal adult immune system', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(403781, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0100546', 'abnormal whole organism', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(403782, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0131730', 'abnormal regulation of protein folding', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(403783, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0100108', 'abnormal cell part', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(403784, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0100585', 'abnormal elastica externa', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(403785, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0115505', 'dead whole organism', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(403786, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0115508', 'abnormally peramorphic growth of whole organism', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(403787, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0141794', 'abnormal prosthetic group metabolic process', 0.5238095238095238, 4.758907843651163, 1.5788480773767701, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(403788, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0100704', 'abnormal Merkel cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(403789, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0100026', 'abnormal germ cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(403790, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0141315', 'abnormal anatomical region', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(403791, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0141877', 'abnormal 2-deoxyribose 1-phosphate metabolic process', 0.4583333333333333, 4.758907843651163, 1.4768771428276568, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(403792, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0101113', 'abnormal stage IV oocyte', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(403793, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0141784', 'abnormal cellular hormone metabolic process', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(403794, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0141852', 'abnormal glucose metabolic process', 0.4230769230769231, 4.758907843651163, 1.418937661667548, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(403795, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0100581', 'abnormal immune system', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(403796, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0101141', 'abnormal Keller explant', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(403797, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0141745', 'abnormal creatinine homeostasis', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(403798, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0101004', 'abnormal acid secreting cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(403799, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0128000', 'absent behavior', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(403800, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0107270', 'abnormal proximal-distal axis', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(403801, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0101157', 'abnormal female organism', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(403802, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0101498', 'abnormal stage II oocyte', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(403803, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0141892', 'abnormal inositol metabolic process', 0.4782608695652174, 4.758907843651163, 1.508641575552437, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(403804, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0100791', 'abnormal multiciliated cell precursor', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(403805, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0100638', 'abnormal polar body', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(403806, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0141907', 'abnormal putrescine metabolic process', 0.4782608695652174, 4.758907843651163, 1.508641575552437, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(403807, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0100377', 'abnormal connective tissue', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(403808, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0107262', 'abnormal left-right axis', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(403809, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0101132', 'abnormal apoptotic cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(403810, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0100888', 'abnormal microtubule', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(403811, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0101569', 'abnormal activin-induced ectoderm', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(403812, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0101220', 'abnormal centriole', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(403813, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0100274', 'abnormal sensory system', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(403814, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0141748', 'abnormal gas homeostasis', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(403815, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0101240', 'abnormal ciliated non-epidermal cell', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(403816, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0141775', 'abnormal nitrogen compound metabolic process', 0.5238095238095238, 4.758907843651163, 1.5788480773767701, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(403817, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0107312', 'abnormal filopodium', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(403818, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0107261', 'abnormal dorsal-ventral axis', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(403819, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0141499', 'abnormal tadpole', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(403820, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0141860', 'abnormal malate-aspartate shuttle', 0.5, 4.758907843651163, 1.5425478669479211, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(403821, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0100202', 'abnormal embryo', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(403822, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0141798', 'abnormal lipid metabolic process', 0.4782608695652174, 4.758907843651163, 1.508641575552437, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(403823, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0141771', 'abnormal urea homeostasis', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(403824, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0141772', 'abnormal water homeostasis', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(403825, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0141795', 'abnormal glycosylation', 0.4782608695652174, 4.758907843651163, 1.508641575552437, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(403826, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0100429', 'abnormal spermatid', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(403827, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0101513', 'abnormal basal body', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(403828, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0100081', 'abnormal anatomical entity in vitro', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(403829, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0131666', 'abnormal adherens junction', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(403830, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0141776', 'abnormal metabolic process', 0.5789473684210527, 4.758907843651163, 1.6598666129060333, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(403831, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0131725', 'abnormal phosphorylation of RNA polymerase II C-terminal domain', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(403832, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0100307', 'abnormal blastomere', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(403833, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0141898', 'abnormal maltose metabolic process', 0.4583333333333333, 4.758907843651163, 1.4768771428276568, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(403834, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0101366', 'abnormal morula cell', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(403835, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0131694', 'abnormal RNA polymerase II activity', 0.4583333333333333, 4.758907843651163, 1.4768771428276568, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(403836, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0100031', 'abnormal central nervous system', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(403837, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0141754', 'abnormal homeostatic process', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(403838, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0116494', 'absent biological process', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(403839, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0100232', 'abnormal lymphatic system', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(403840, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0141743', 'abnormal chemical homeostasis within a tissue', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(403841, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0141738', 'abnormal carbon dioxide homeostasis', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(403842, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0101326', 'abnormal cementoblast', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(403843, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0141263', 'abnormal visually guided collision avoidance behavior', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(403844, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0131685', 'abnormal cortical actin cytoskeleton', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(403845, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0101264', 'abnormal mitotic spindle', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(403846, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0100032', 'abnormal nervous system', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(403847, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0101547', 'abnormal lampbrush chromosome', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(403848, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0142057', 'abnormal desmosome', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(403849, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0100225', 'abnormal endocrine system', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(403850, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0141903', 'abnormal inositol phosphate metabolic process', 0.4230769230769231, 4.758907843651163, 1.418937661667548, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(403851, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0141266', 'abnormal surface breathing', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(403852, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0141872', 'abnormal cholesterol metabolic process', 0.4074074074074074, 4.758907843651163, 1.392413123563799, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(403853, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0100176', 'abnormal stage VI oocyte', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(403854, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0141911', 'abnormal ribose phosphate metabolic process', 0.4583333333333333, 4.758907843651163, 1.4768771428276568, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(403855, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0101435', 'abnormal paracrine cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(403856, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0100025', 'abnormal oocyte', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(403857, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0101468', 'abnormal stage I oocyte', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(403858, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0141781', 'abnormal secondary metabolic process', 0.5238095238095238, 4.758907843651163, 1.5788480773767701, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(403859, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0141908', 'abnormal pyridine metabolic process', 0.4230769230769231, 4.758907843651163, 1.418937661667548, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(403860, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0100337', 'abnormal zygote', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(403861, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0115512', 'abnormally semi-erect whole organism', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(403862, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0107258', 'abnormal anatomical axis', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(403863, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0141782', 'abnormal methylation', 0.5238095238095238, 4.758907843651163, 1.5788480773767701, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(403864, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0100899', 'abnormal secondary spermatogonium', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(403865, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0101535', 'abnormal absorptive cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(403866, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0131745', 'abnormal axis elongation', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(403867, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0101448', 'abnormal myelin accumulating cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(403868, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0141883', 'abnormal glycerol metabolic process', 0.4230769230769231, 4.758907843651163, 1.418937661667548, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(403869, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0141809', 'abnormal catalytic activity', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(403870, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0100545', 'abnormal male organism', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(403871, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0141786', 'abnormal pigment metabolic process', 0.5238095238095238, 4.758907843651163, 1.5788480773767701, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(403872, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0141850', 'abnormal galactose metabolic process', 0.4230769230769231, 4.758907843651163, 1.418937661667548, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(403873, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0101061', 'abnormal plasma membrane', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(403874, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0100004', 'abnormal cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(403875, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0115509', 'abnormally semi-viable whole organism', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(403876, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0141880', 'abnormal ethanolamine metabolic process', 0.44, 4.758907843651163, 1.447038165082909, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(403877, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0141881', 'abnormal fructose metabolic process', 0.4230769230769231, 4.758907843651163, 1.418937661667548, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(403878, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0131675', 'abnormal spindle microtubule', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(403879, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0100501', 'abnormal urogenital system', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(403880, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0101409', 'abnormal perivitelline space', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(403881, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0141788', 'abnormal hormone biosynthetic process', 0.44, 4.758907843651163, 1.447038165082909, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(403882, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0141271', 'increased surface breathing', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(403883, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0101228', 'abnormal mesenchymal stem cell', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(403884, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0131729', 'abnormal regulation of growth rate', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(403885, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0141783', 'abnormal collagen metabolic process', 0.5238095238095238, 4.758907843651163, 1.5788480773767701, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(403886, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0100573', 'abnormal extraembryonic structure', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(403887, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0101241', 'abnormal nucleate erythrocyte', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(403888, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0100285', 'abnormal progenitor cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(403889, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0100802', 'abnormal exocrine cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(403890, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0101109', 'abnormal egg cell-free extract', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(403891, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0141797', 'abnormal hydrogen metabolic process', 0.5238095238095238, 4.758907843651163, 1.5788480773767701, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(403892, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0100392', 'abnormal cilium', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(403893, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0100289', 'abnormal chondroblast', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(403894, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0100902', 'abnormal spermatocyte', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(403895, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0100308', 'abnormal early embryonic cell', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(403896, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0141904', 'abnormal glucosamine metabolic process', 0.5238095238095238, 4.758907843651163, 1.5788480773767701, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(403897, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0100574', 'abnormal gastrula cell', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(403898, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0100533', 'abnormal melanoblast', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(403899, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0133388', 'absent insulin receptor signaling pathway', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(403900, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0141778', 'abnormal biosynthetic process', 0.5238095238095238, 4.758907843651163, 1.5788480773767701, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(403901, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0141276', 'decreased surface breathing', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(403902, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0101480', 'abnormal stage V oocyte', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(403903, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0141791', 'abnormal primary metabolic process', 0.5238095238095238, 4.758907843651163, 1.5788480773767701, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(403904, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0100317', 'abnormal respiratory system', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(403905, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0100062', 'abnormal anatomical space', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(403906, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0100477', 'abnormal pericyte', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(403907, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0100715', 'abnormal ciliated cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(403908, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0100423', 'abnormal process', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(403909, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0100674', 'abnormal secondary oogonium', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(403910, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0141789', 'abnormal hormone catabolic process', 0.44, 4.758907843651163, 1.447038165082909, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(403911, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0141900', 'abnormal mannose metabolic process', 0.4230769230769231, 4.758907843651163, 1.418937661667548, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(403912, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0101071', 'abnormal endoplasmic reticulum', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(403913, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0100515', 'abnormal somatic stem cell', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(403914, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0141265', 'abnormal escape behavior', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(403915, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0100084', 'abnormal anatomical group', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(403916, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0141264', 'abnormal schooling behavior', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(403917, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0101237', 'abnormal mucus secreting cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(403918, 'HP:0025433', 'Decreased lecithin cholesterol acyl transferase level', 'XPO:0107259', 'abnormal animal-vegetal axis', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(403919, 'HP:3000056', 'Abnormality of artery of lower lip', 'XPO:0130702', 'increased size of the ophthalmic artery', 0.43529411764705883, 11.341685124041394, 2.2219290759833834, 'UPHENO:0087623', 'abnormal carotid artery segment morphology'),
(403920, 'HP:3000056', 'Abnormality of artery of lower lip', 'XPO:0139803', 'abnormally necrotic aorta', 0.4166666666666667, 9.08792853179561, 1.945928284456591, 'UPHENO:0087334', 'abnormal systemic artery morphology'),
(403921, 'HP:3000056', 'Abnormality of artery of lower lip', 'XPO:0103091', 'abnormal arteria iliaca communis morphology', 0.42857142857142855, 9.08792853179561, 1.973531482806061, 'UPHENO:0087334', 'abnormal systemic artery morphology'),
(403922, 'HP:3000056', 'Abnormality of artery of lower lip', 'XPO:0141159', 'abnormally necrotic posterior palatine artery', 0.47435897435897434, 11.341685124041394, 2.319489194400938, 'UPHENO:0087623', 'abnormal carotid artery segment morphology'),
(403923, 'HP:3000056', 'Abnormality of artery of lower lip', 'XPO:0102777', 'abnormal maxillary artery morphology', 0.43478260869565216, 9.01729298920255, 1.9800409513993644, 'UPHENO:0015290', 'abnormal artery morphology in the independent continuant'),
(403924, 'HP:3000056', 'Abnormality of artery of lower lip', 'XPO:0129226', 'decreased size of the ophthalmic artery', 0.43529411764705883, 11.341685124041394, 2.2219290759833834, 'UPHENO:0087623', 'abnormal carotid artery segment morphology'),
(403925, 'HP:3000056', 'Abnormality of artery of lower lip', 'XPO:0102613', 'abnormal dorsal longitudinal anastomosing vessel morphology', 0.4067796610169492, 6.974839882869777, 1.6844058309093048, 'UPHENO:0087186', 'abnormal blood vessel morphology'),
(403926, 'HP:3000056', 'Abnormality of artery of lower lip', 'XPO:0102433', 'abnormal vena capitis lateralis morphology', 0.4027777777777778, 7.803720102857406, 1.77289735783792, 'HP:0033353', 'Abnormal blood vessel morphology'),
(403927, 'HP:3000056', 'Abnormality of artery of lower lip', 'XPO:0103003', 'abnormal facial vein morphology', 0.4027777777777778, 7.803720102857406, 1.77289735783792, 'HP:0033353', 'Abnormal blood vessel morphology'),
(403928, 'HP:3000056', 'Abnormality of artery of lower lip', 'XPO:0125718', 'absent external carotid artery', 0.4342105263157895, 13.819732420846037, 2.4496271732651356, 'UPHENO:0004442', 'abnormal external carotid artery'),
(403929, 'HP:3000056', 'Abnormality of artery of lower lip', 'XPO:0102225', 'abnormal cerebral artery morphology', 0.42528735632183906, 11.341685124041394, 2.19624117132848, 'UPHENO:0087623', 'abnormal carotid artery segment morphology'),
(403930, 'HP:3000056', 'Abnormality of artery of lower lip', 'XPO:0127028', 'abnormally localised ophthalmic artery', 0.46835443037974683, 11.341685124041394, 2.304762129985838, 'UPHENO:0087623', 'abnormal carotid artery segment morphology'),
(403931, 'HP:3000056', 'Abnormality of artery of lower lip', 'XPO:0129044', 'decreased size of the posterior palatine artery', 0.4625, 11.341685124041394, 2.290312068227635, 'UPHENO:0087623', 'abnormal carotid artery segment morphology'),
(403932, 'HP:3000056', 'Abnormality of artery of lower lip', 'XPO:0102424', 'abnormal capillary morphology', 0.4032258064516129, 7.803720102857406, 1.7738831223610367, 'HP:0033353', 'Abnormal blood vessel morphology'),
(403933, 'HP:3000056', 'Abnormality of artery of lower lip', 'XPO:0129573', 'increased size of the aorta', 0.40540540540540543, 9.08792853179561, 1.9194518360010886, 'UPHENO:0087334', 'abnormal systemic artery morphology'),
(403934, 'HP:3000056', 'Abnormality of artery of lower lip', 'XPO:0129254', 'decreased size of the anterior palatine artery', 0.4625, 11.341685124041394, 2.290312068227635, 'UPHENO:0087623', 'abnormal carotid artery segment morphology'),
(403935, 'HP:3000056', 'Abnormality of artery of lower lip', 'XPO:0101774', 'abnormal paired dorsal aorta morphology', 0.44776119402985076, 9.08792853179561, 2.0172312040653027, 'UPHENO:0087334', 'abnormal systemic artery morphology'),
(403936, 'HP:3000056', 'Abnormality of artery of lower lip', 'XPO:0101686', 'abnormal blood vessel morphology', 0.42105263157894735, 6.974839882869777, 1.7137020416408788, 'UPHENO:0087186', 'abnormal blood vessel morphology'),
(403937, 'HP:3000056', 'Abnormality of artery of lower lip', 'XPO:0102619', 'abnormal larval aorta morphology', 0.4262295081967213, 9.01729298920255, 1.960468402207377, 'UPHENO:0015290', 'abnormal artery morphology in the independent continuant'),
(403938, 'HP:3000056', 'Abnormality of artery of lower lip', 'XPO:0102786', 'abnormal external carotid artery morphology', 0.47368421052631576, 14.124587002374458, 2.586618225256678, 'UPHENO:0087321', 'abnormal external carotid artery morphology'),
(403939, 'HP:3000056', 'Abnormality of artery of lower lip', 'XPO:0101840', 'abnormal ventral aorta morphology', 0.4166666666666667, 9.08792853179561, 1.945928284456591, 'UPHENO:0087334', 'abnormal systemic artery morphology'),
(403940, 'HP:3000056', 'Abnormality of artery of lower lip', 'XPO:0100955', 'abnormal internal jugular vein', 0.4027777777777778, 7.803720102857406, 1.77289735783792, 'HP:0033353', 'Abnormal blood vessel morphology'),
(403941, 'HP:3000056', 'Abnormality of artery of lower lip', 'XPO:0101052', 'abnormal ophthalmic artery', 0.5362318840579711, 11.341685124041394, 2.4661251351983298, 'UPHENO:0087623', 'abnormal carotid artery segment morphology'),
(403942, 'HP:3000056', 'Abnormality of artery of lower lip', 'XPO:0130730', 'increased size of the anterior palatine artery', 0.4625, 11.341685124041394, 2.290312068227635, 'UPHENO:0087623', 'abnormal carotid artery segment morphology'),
(403943, 'HP:3000056', 'Abnormality of artery of lower lip', 'XPO:0140689', 'abnormally necrotic anterior palatine artery', 0.47435897435897434, 11.341685124041394, 2.319489194400938, 'UPHENO:0087623', 'abnormal carotid artery segment morphology'),
(403944, 'HP:3000056', 'Abnormality of artery of lower lip', 'XPO:0103001', 'abnormal nasociliary artery morphology', 0.43478260869565216, 9.01729298920255, 1.9800409513993644, 'UPHENO:0015290', 'abnormal artery morphology in the independent continuant'),
(403945, 'HP:3000056', 'Abnormality of artery of lower lip', 'XPO:0129345', 'decreased size of the external carotid artery', 0.4235294117647059, 14.124587002374458, 2.4458491418186576, 'UPHENO:0087321', 'abnormal external carotid artery morphology'),
(403946, 'HP:3000056', 'Abnormality of artery of lower lip', 'XPO:0103063', 'abnormal ischiadic artery morphology', 0.4262295081967213, 9.01729298920255, 1.960468402207377, 'UPHENO:0015290', 'abnormal artery morphology in the independent continuant'),
(403947, 'HP:3000056', 'Abnormality of artery of lower lip', 'XPO:0102503', 'abnormal posterior palatine artery morphology', 0.5211267605633803, 11.341685124041394, 2.4311428645847966, 'UPHENO:0087623', 'abnormal carotid artery segment morphology'),
(403948, 'HP:3000056', 'Abnormality of artery of lower lip', 'XPO:0130521', 'increased size of the posterior palatine artery', 0.4625, 11.341685124041394, 2.290312068227635, 'UPHENO:0087623', 'abnormal carotid artery segment morphology'),
(403949, 'HP:3000056', 'Abnormality of artery of lower lip', 'XPO:0141008', 'abnormally necrotic external carotid artery', 0.43373493975903615, 14.124587002374458, 2.4751417924224364, 'UPHENO:0087321', 'abnormal external carotid artery morphology'),
(403950, 'HP:3000056', 'Abnormality of artery of lower lip', 'XPO:0102875', 'abnormal vertebral artery morphology', 0.4262295081967213, 9.01729298920255, 1.960468402207377, 'UPHENO:0015290', 'abnormal artery morphology in the independent continuant'),
(403951, 'HP:3000056', 'Abnormality of artery of lower lip', 'XPO:0101675', 'abnormal vein morphology', 0.4032258064516129, 7.803720102857406, 1.7738831223610367, 'HP:0033353', 'Abnormal blood vessel morphology'),
(403952, 'HP:3000056', 'Abnormality of artery of lower lip', 'XPO:0128093', 'decreased size of the aorta', 0.40540540540540543, 9.08792853179561, 1.9194518360010886, 'UPHENO:0087334', 'abnormal systemic artery morphology'),
(403953, 'HP:3000056', 'Abnormality of artery of lower lip', 'XPO:0101708', 'abnormal artery morphology', 0.4406779661016949, 9.01729298920255, 1.9934197586621973, 'UPHENO:0015290', 'abnormal artery morphology in the independent continuant'),
(403954, 'HP:3000056', 'Abnormality of artery of lower lip', 'XPO:0129796', 'increased size of the internal carotid artery', 0.4567901234567901, 11.341685124041394, 2.2761304329978342, 'UPHENO:0087623', 'abnormal carotid artery segment morphology'),
(403955, 'HP:3000056', 'Abnormality of artery of lower lip', 'XPO:0102329', 'abnormal caudal artery morphology', 0.4225352112676056, 9.08792853179561, 1.9595840890778735, 'UPHENO:0087334', 'abnormal systemic artery morphology'),
(403956, 'HP:3000056', 'Abnormality of artery of lower lip', 'XPO:0101685', 'abnormal head vasculature morphology', 0.42857142857142855, 6.65602285090012, 1.688958620515712, 'HP:0025015', 'Abnormal vascular morphology'),
(403957, 'HP:3000056', 'Abnormality of artery of lower lip', 'XPO:0102421', 'abnormal occipitovertebral artery morphology', 0.4262295081967213, 9.01729298920255, 1.960468402207377, 'UPHENO:0015290', 'abnormal artery morphology in the independent continuant'),
(403958, 'HP:3000056', 'Abnormality of artery of lower lip', 'XPO:0140107', 'abnormally necrotic internal carotid artery', 0.46835443037974683, 11.341685124041394, 2.304762129985838, 'UPHENO:0087623', 'abnormal carotid artery segment morphology'),
(403959, 'HP:3000056', 'Abnormality of artery of lower lip', 'XPO:0101780', 'abnormal arteria mesenterica posterior morphology', 0.4166666666666667, 9.08792853179561, 1.945928284456591, 'UPHENO:0087334', 'abnormal systemic artery morphology'),
(403960, 'HP:3000056', 'Abnormality of artery of lower lip', 'XPO:0102443', 'abnormal vena capitis medialis morphology', 0.4027777777777778, 7.803720102857406, 1.77289735783792, 'HP:0033353', 'Abnormal blood vessel morphology'),
(403961, 'HP:3000056', 'Abnormality of artery of lower lip', 'XPO:0102684', 'abnormal ophthalmic artery morphology', 0.4868421052631579, 11.341685124041394, 2.3498106015209297, 'UPHENO:0087623', 'abnormal carotid artery segment morphology'),
(403962, 'HP:3000056', 'Abnormality of artery of lower lip', 'XPO:0102802', 'abnormal arteria subclavia morphology', 0.40298507462686567, 9.08792853179561, 1.9137135516030803, 'UPHENO:0087334', 'abnormal systemic artery morphology'),
(403963, 'HP:3000056', 'Abnormality of artery of lower lip', 'XPO:0102074', 'abnormal internal carotid artery morphology', 0.5138888888888888, 11.341685124041394, 2.414200896056762, 'UPHENO:0087623', 'abnormal carotid artery segment morphology'),
(403964, 'HP:3000056', 'Abnormality of artery of lower lip', 'XPO:0130820', 'increased size of the external carotid artery', 0.4235294117647059, 14.124587002374458, 2.4458491418186576, 'UPHENO:0087321', 'abnormal external carotid artery morphology'),
(403965, 'HP:3000056', 'Abnormality of artery of lower lip', 'XPO:0101712', 'abnormal aorta morphology', 0.46153846153846156, 9.08792853179561, 2.0480304082548275, 'UPHENO:0087334', 'abnormal systemic artery morphology'),
(403966, 'HP:3000056', 'Abnormality of artery of lower lip', 'XPO:0125393', 'absent ophthalmic artery', 0.4567901234567901, 11.341685124041394, 2.2761304329978342, 'UPHENO:0087623', 'abnormal carotid artery segment morphology'),
(403967, 'HP:3000056', 'Abnormality of artery of lower lip', 'XPO:0127366', 'abnormally localised external carotid artery', 0.44594594594594594, 13.819732420846037, 2.482509546232208, 'UPHENO:0004442', 'abnormal external carotid artery'),
(403968, 'HP:3000056', 'Abnormality of artery of lower lip', 'XPO:0101711', 'abnormal dorsal aorta morphology', 0.4166666666666667, 9.08792853179561, 1.945928284456591, 'UPHENO:0087334', 'abnormal systemic artery morphology'),
(403969, 'HP:3000056', 'Abnormality of artery of lower lip', 'XPO:0103215', 'abnormal truncus arteriosus morphology', 0.4067796610169492, 6.974839882869777, 1.6844058309093048, 'UPHENO:0087186', 'abnormal blood vessel morphology'),
(403970, 'HP:3000056', 'Abnormality of artery of lower lip', 'XPO:0141139', 'abnormally necrotic ophthalmic artery', 0.4457831325301205, 11.341685124041394, 2.2485399535621866, 'UPHENO:0087623', 'abnormal carotid artery segment morphology'),
(403971, 'HP:3000056', 'Abnormality of artery of lower lip', 'XPO:0128316', 'decreased size of the internal carotid artery', 0.4567901234567901, 11.341685124041394, 2.2761304329978342, 'UPHENO:0087623', 'abnormal carotid artery segment morphology'),
(403972, 'HP:3000056', 'Abnormality of artery of lower lip', 'XPO:0102050', 'abnormal anterior palatine artery morphology', 0.5211267605633803, 11.341685124041394, 2.4311428645847966, 'UPHENO:0087623', 'abnormal carotid artery segment morphology'),
(403973, 'HP:3000056', 'Abnormality of artery of lower lip', 'XPO:0101154', 'abnormal external carotid artery', 0.515625, 13.819732420846037, 2.6694193244034814, 'UPHENO:0004442', 'abnormal external carotid artery'),
(403974, 'HP:3000056', 'Abnormality of artery of lower lip', 'XPO:0101707', 'abnormal mandibular artery morphology', 0.43478260869565216, 9.01729298920255, 1.9800409513993644, 'UPHENO:0015290', 'abnormal artery morphology in the independent continuant'),
(403975, 'HP:0100543', 'Cognitive impairment', 'XPO:0100477', 'abnormal pericyte', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(403976, 'HP:0100543', 'Cognitive impairment', 'XPO:0100358', 'abnormal ganglion', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(403977, 'HP:0100543', 'Cognitive impairment', 'XPO:0101297', 'abnormal barrier cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(403978, 'HP:0100543', 'Cognitive impairment', 'XPO:0101004', 'abnormal acid secreting cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(403979, 'HP:0100543', 'Cognitive impairment', 'XPO:0101132', 'abnormal apoptotic cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(403980, 'HP:0100543', 'Cognitive impairment', 'XPO:0100791', 'abnormal multiciliated cell precursor', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(403981, 'HP:0100543', 'Cognitive impairment', 'XPO:0100006', 'abnormal anatomical structure', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(403982, 'HP:0100543', 'Cognitive impairment', 'XPO:0100026', 'abnormal germ cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(403983, 'HP:0100543', 'Cognitive impairment', 'XPO:0100734', 'abnormal lateral line system', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(403984, 'HP:0100543', 'Cognitive impairment', 'XPO:0101448', 'abnormal myelin accumulating cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(403985, 'HP:0100543', 'Cognitive impairment', 'XPO:0100704', 'abnormal Merkel cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(403986, 'HP:0100543', 'Cognitive impairment', 'XPO:0107286', 'abnormal efferent neuron', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(403987, 'HP:0100543', 'Cognitive impairment', 'XPO:0100858', 'abnormal presumptive midbrain-hindbrain boundary', 0.43333333333333335, 3.94131651835137, 1.3068679445984308, 'UPHENO:0004523', 'abnormal nervous system'),
(403988, 'HP:0100543', 'Cognitive impairment', 'XPO:0100537', 'abnormal medium cavity', 0.43333333333333335, 3.94131651835137, 1.3068679445984308, 'UPHENO:0004523', 'abnormal nervous system'),
(403989, 'HP:0100543', 'Cognitive impairment', 'XPO:0126887', 'abnormally localised nervous system', 0.4117647058823529, 3.94131651835137, 1.2739289764222381, 'UPHENO:0004523', 'abnormal nervous system'),
(403990, 'HP:0100543', 'Cognitive impairment', 'XPO:0100954', 'abnormal neural progenitor cell', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(403991, 'HP:0100543', 'Cognitive impairment', 'XPO:0100285', 'abnormal progenitor cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(403992, 'HP:0100543', 'Cognitive impairment', 'XPO:0101535', 'abnormal absorptive cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(403993, 'HP:0100543', 'Cognitive impairment', 'XPO:0100549', 'abnormal mitotic cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(403994, 'HP:0100543', 'Cognitive impairment', 'XPO:0101373', 'abnormal oxygen accumulating cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(403995, 'HP:0100543', 'Cognitive impairment', 'XPO:0131654', 'abnormal neuron projection', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(403996, 'HP:0100543', 'Cognitive impairment', 'XPO:0100754', 'abnormal electrically active cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(403997, 'HP:0100543', 'Cognitive impairment', 'XPO:0100427', 'abnormal olfactory system', 0.4642857142857143, 3.94131651835137, 1.3527368387638634, 'UPHENO:0004523', 'abnormal nervous system'),
(403998, 'HP:0100543', 'Cognitive impairment', 'XPO:0100172', 'abnormal stem cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(403999, 'HP:0100543', 'Cognitive impairment', 'XPO:0100164', 'abnormal neural nucleus', 0.4482758620689655, 3.94131651835137, 1.3292091859262085, 'UPHENO:0004523', 'abnormal nervous system'),
(404000, 'HP:0100543', 'Cognitive impairment', 'XPO:0142051', 'abnormal cerebrospinal fluid', 0.4482758620689655, 3.94131651835137, 1.3292091859262085, 'UPHENO:0004523', 'abnormal nervous system'),
(404001, 'HP:0100543', 'Cognitive impairment', 'XPO:0100864', 'abnormal dorsolateral ascending neuron', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(404002, 'HP:0100543', 'Cognitive impairment', 'XPO:0100701', 'abnormal microglial cell', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(404003, 'HP:0100543', 'Cognitive impairment', 'XPO:0100802', 'abnormal exocrine cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(404004, 'HP:0100543', 'Cognitive impairment', 'XPO:0100274', 'abnormal sensory system', 0.48148148148148145, 3.94131651835137, 1.3775597686645948, 'UPHENO:0004523', 'abnormal nervous system'),
(404005, 'HP:0100543', 'Cognitive impairment', 'XPO:0100108', 'abnormal cell part', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(404006, 'HP:0100543', 'Cognitive impairment', 'XPO:0100336', 'abnormal interneuron', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(404007, 'HP:0100543', 'Cognitive impairment', 'XPO:0100642', 'abnormal gustatory system', 0.4642857142857143, 3.94131651835137, 1.3527368387638634, 'UPHENO:0004523', 'abnormal nervous system'),
(404008, 'HP:0100543', 'Cognitive impairment', 'XPO:0101467', 'abnormal alkali secreting cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(404009, 'HP:0100543', 'Cognitive impairment', 'XPO:0100158', 'abnormal neuromere', 0.43333333333333335, 3.94131651835137, 1.3068679445984308, 'UPHENO:0004523', 'abnormal nervous system'),
(404010, 'HP:0100543', 'Cognitive impairment', 'XPO:0101241', 'abnormal nucleate erythrocyte', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(404011, 'HP:0100543', 'Cognitive impairment', 'XPO:0107253', 'abnormal enteric nervous system', 0.48148148148148145, 3.94131651835137, 1.3775597686645948, 'UPHENO:0004523', 'abnormal nervous system'),
(404012, 'HP:0100543', 'Cognitive impairment', 'XPO:0101237', 'abnormal mucus secreting cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(404013, 'HP:0100543', 'Cognitive impairment', 'XPO:0100691', 'abnormal keratin accumulating cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(404014, 'HP:0100543', 'Cognitive impairment', 'XPO:0101333', 'abnormal barrier epithelial cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(404015, 'HP:0100543', 'Cognitive impairment', 'XPO:0100004', 'abnormal cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(404016, 'HP:0100543', 'Cognitive impairment', 'XPO:0107287', 'abnormal afferent neuron', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(404017, 'HP:0100543', 'Cognitive impairment', 'XPO:0100196', 'abnormal neuron', 0.43333333333333335, 3.94131651835137, 1.3068679445984308, 'UPHENO:0004523', 'abnormal nervous system'),
(404018, 'HP:0100543', 'Cognitive impairment', 'XPO:0100273', 'abnormal visual system', 0.4642857142857143, 3.94131651835137, 1.3527368387638634, 'UPHENO:0004523', 'abnormal nervous system'),
(404019, 'HP:0100543', 'Cognitive impairment', 'XPO:0101133', 'abnormal motor neuron', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(404020, 'HP:0100543', 'Cognitive impairment', 'XPO:0101239', 'abnormal olfactory epithelial support cell', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(404021, 'HP:0100543', 'Cognitive impairment', 'XPO:0100031', 'abnormal central nervous system', 0.48148148148148145, 3.94131651835137, 1.3775597686645948, 'UPHENO:0004523', 'abnormal nervous system'),
(404022, 'HP:0100543', 'Cognitive impairment', 'XPO:0101326', 'abnormal cementoblast', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(404023, 'HP:0100543', 'Cognitive impairment', 'XPO:0100081', 'abnormal anatomical entity in vitro', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(404024, 'HP:0100543', 'Cognitive impairment', 'XPO:0100344', 'abnormal portion of organism substance', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(404025, 'HP:0100543', 'Cognitive impairment', 'XPO:0100760', 'abnormal Stirnorgan', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(404026, 'HP:0100543', 'Cognitive impairment', 'XPO:0100337', 'abnormal zygote', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(404027, 'HP:0100543', 'Cognitive impairment', 'XPO:0100653', 'abnormal myoblast', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(404028, 'HP:0100543', 'Cognitive impairment', 'XPO:0100702', 'abnormal glial cell', 0.43333333333333335, 3.94131651835137, 1.3068679445984308, 'UPHENO:0004523', 'abnormal nervous system'),
(404029, 'HP:0100543', 'Cognitive impairment', 'XPO:0101435', 'abnormal paracrine cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(404030, 'HP:0100543', 'Cognitive impairment', 'XPO:0100715', 'abnormal ciliated cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(404031, 'HP:0100543', 'Cognitive impairment', 'XPO:0100533', 'abnormal melanoblast', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(404032, 'HP:0100543', 'Cognitive impairment', 'XPO:0100916', 'abnormal principal cavity', 0.43333333333333335, 3.94131651835137, 1.3068679445984308, 'UPHENO:0004523', 'abnormal nervous system'),
(404033, 'HP:0100543', 'Cognitive impairment', 'XPO:0100289', 'abnormal chondroblast', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(404034, 'HP:0100543', 'Cognitive impairment', 'XPO:0100852', 'abnormal interdigital region', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(404035, 'HP:0100543', 'Cognitive impairment', 'XPO:0100587', 'abnormal vestibuloauditory system', 0.4642857142857143, 3.94131651835137, 1.3527368387638634, 'UPHENO:0004523', 'abnormal nervous system'),
(404036, 'HP:0100543', 'Cognitive impairment', 'XPO:0100032', 'abnormal nervous system', 0.5, 3.94131651835137, 1.4038013602984167, 'UPHENO:0004523', 'abnormal nervous system'),
(404037, 'HP:0100543', 'Cognitive impairment', 'XPO:0101501', 'abnormal parabrachial area', 0.43333333333333335, 3.94131651835137, 1.3068679445984308, 'UPHENO:0004523', 'abnormal nervous system'),
(404038, 'HP:0100543', 'Cognitive impairment', 'XPO:0100481', 'abnormal anatomical line', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(404039, 'HP:0100543', 'Cognitive impairment', 'XPO:0101187', 'abnormal dorsolateral commissural neuron', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(404040, 'HP:0100543', 'Cognitive impairment', 'XPO:0100175', 'abnormal migrating neuroblast', 0.43333333333333335, 3.94131651835137, 1.3068679445984308, 'UPHENO:0004523', 'abnormal nervous system'),
(404041, 'HP:0100543', 'Cognitive impairment', 'XPO:0100114', 'abnormal peripheral nervous system', 0.4482758620689655, 3.94131651835137, 1.3292091859262085, 'UPHENO:0004523', 'abnormal nervous system'),
(404042, 'HP:0100543', 'Cognitive impairment', 'XPO:0100638', 'abnormal polar body', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(404043, 'HP:0100543', 'Cognitive impairment', 'XPO:0100056', 'abnormal olfactory epithelium', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(404044, 'HP:0100543', 'Cognitive impairment', 'XPO:0100438', 'abnormal spinal cord', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(404045, 'HP:0410182', 'Decreased glucose-6-phosphate dehydrogenase level in dried blood spot', 'XPO:0141873', 'abnormal tricarboxylic acid metabolic process', 0.40350877192982454, 7.41682187759612, 1.729957423594889, 'HP:0430071', 'Abnormal circulating organic compound concentration'),
(404046, 'HP:0008060', 'Aplasia/Hypoplasia of the fovea', 'XPO:0140948', 'abnormally necrotic retinal inner nuclear layer', 0.42574257425742573, 8.040873045973026, 1.850227550835222, 'HP:0000479', 'Abnormal retinal morphology'),
(404047, 'HP:0008060', 'Aplasia/Hypoplasia of the fovea', 'XPO:0128300', 'decreased size of the retina', 0.4942528735632184, 8.040873045973026, 1.9935457378573478, 'HP:0000479', 'Abnormal retinal morphology'),
(404048, 'HP:0008060', 'Aplasia/Hypoplasia of the fovea', 'XPO:0128330', 'decreased size of the retinal progenitor cell region', 0.48314606741573035, 8.040873045973026, 1.9710190741722953, 'HP:0000479', 'Abnormal retinal morphology'),
(404049, 'HP:0008060', 'Aplasia/Hypoplasia of the fovea', 'XPO:0133354', 'fused eyes', 0.4166666666666667, 6.887869297006056, 1.6940913612964297, 'HP:0012372', 'Abnormal eye morphology'),
(404050, 'HP:0008060', 'Aplasia/Hypoplasia of the fovea', 'XPO:0130265', 'increased size of the peripheral retina', 0.4725274725274725, 8.040873045973026, 1.9492391893577128, 'HP:0000479', 'Abnormal retinal morphology'),
(404051, 'HP:0008060', 'Aplasia/Hypoplasia of the fovea', 'XPO:0103226', 'abnormal retinal outer plexiform layer morphology', 0.4574468085106383, 8.040873045973026, 1.9178820903589395, 'HP:0000479', 'Abnormal retinal morphology'),
(404052, 'HP:0008060', 'Aplasia/Hypoplasia of the fovea', 'XPO:0141138', 'abnormally necrotic retinal inner plexiform layer', 0.42574257425742573, 8.040873045973026, 1.850227550835222, 'HP:0000479', 'Abnormal retinal morphology'),
(404053, 'HP:0008060', 'Aplasia/Hypoplasia of the fovea', 'XPO:0128100', 'decreased size of the inner limiting membrane', 0.4215686274509804, 8.040873045973026, 1.8411354685352277, 'HP:0000479', 'Abnormal retinal morphology'),
(404054, 'HP:0008060', 'Aplasia/Hypoplasia of the fovea', 'XPO:0102756', 'abnormal Muller cell morphology', 0.48863636363636365, 8.040873045973026, 1.982186410418029, 'HP:0000479', 'Abnormal retinal morphology'),
(404055, 'HP:0008060', 'Aplasia/Hypoplasia of the fovea', 'XPO:0140553', 'abnormally necrotic retinal stem cell region', 0.4942528735632184, 8.040873045973026, 1.9935457378573478, 'HP:0000479', 'Abnormal retinal morphology'),
(404056, 'HP:0008060', 'Aplasia/Hypoplasia of the fovea', 'XPO:0140346', 'abnormally necrotic retinal blood vessel', 0.41346153846153844, 8.040873045973026, 1.8233463028623837, 'HP:0000479', 'Abnormal retinal morphology'),
(404057, 'HP:0008060', 'Aplasia/Hypoplasia of the fovea', 'XPO:0130148', 'increased size of the ciliary marginal zone', 0.4387755102040816, 8.040873045973026, 1.8783338822565765, 'HP:0000479', 'Abnormal retinal morphology'),
(404058, 'HP:0008060', 'Aplasia/Hypoplasia of the fovea', 'XPO:0128935', 'decreased size of the central retina', 0.5058823529411764, 8.040873045973026, 2.0168628550791743, 'HP:0000479', 'Abnormal retinal morphology'),
(404059, 'HP:0008060', 'Aplasia/Hypoplasia of the fovea', 'XPO:0125909', 'absent retinal blood vessel', 0.4574468085106383, 8.040873045973026, 1.9178820903589395, 'HP:0000479', 'Abnormal retinal morphology'),
(404060, 'HP:0008060', 'Aplasia/Hypoplasia of the fovea', 'XPO:0102996', 'abnormal optic fiber layer morphology', 0.4574468085106383, 8.040873045973026, 1.9178820903589395, 'HP:0000479', 'Abnormal retinal morphology'),
(404061, 'HP:0008060', 'Aplasia/Hypoplasia of the fovea', 'XPO:0102805', 'abnormal retinal layer morphology', 0.5512820512820513, 8.040873045973026, 2.1054189575670126, 'HP:0000479', 'Abnormal retinal morphology'),
(404062, 'HP:0008060', 'Aplasia/Hypoplasia of the fovea', 'XPO:0140081', 'abnormally necrotic amacrine cell', 0.40186915887850466, 8.040873045973026, 1.797603651429875, 'HP:0000479', 'Abnormal retinal morphology'),
(404063, 'HP:0008060', 'Aplasia/Hypoplasia of the fovea', 'XPO:0103184', 'abnormal inner limiting membrane morphology', 0.4574468085106383, 8.040873045973026, 1.9178820903589395, 'HP:0000479', 'Abnormal retinal morphology'),
(404064, 'HP:0008060', 'Aplasia/Hypoplasia of the fovea', 'XPO:0141343', 'decreased pigmentation in the eye', 0.4166666666666667, 6.887869297006056, 1.6940913612964297, 'HP:0012372', 'Abnormal eye morphology'),
(404065, 'HP:0008060', 'Aplasia/Hypoplasia of the fovea', 'XPO:0141333', 'increased pigmentation in the retinal pigmented epithelium', 0.44329896907216493, 8.040873045973026, 1.8879911895239345, 'HP:0000479', 'Abnormal retinal morphology'),
(404066, 'HP:0008060', 'Aplasia/Hypoplasia of the fovea', 'XPO:0102939', 'abnormal retinal ganglion cell layer morphology', 0.4574468085106383, 8.040873045973026, 1.9178820903589395, 'HP:0000479', 'Abnormal retinal morphology'),
(404067, 'HP:0008060', 'Aplasia/Hypoplasia of the fovea', 'XPO:0128779', 'decreased size of the retinal blood vessel', 0.4056603773584906, 8.040873045973026, 1.8060630094548564, 'HP:0000479', 'Abnormal retinal morphology'),
(404068, 'HP:0008060', 'Aplasia/Hypoplasia of the fovea', 'XPO:0141182', 'abnormally necrotic inner limiting membrane', 0.42574257425742573, 8.040873045973026, 1.850227550835222, 'HP:0000479', 'Abnormal retinal morphology'),
(404069, 'HP:0008060', 'Aplasia/Hypoplasia of the fovea', 'XPO:0140520', 'abnormally necrotic retinal outer nuclear layer', 0.42574257425742573, 8.040873045973026, 1.850227550835222, 'HP:0000479', 'Abnormal retinal morphology'),
(404070, 'HP:0008060', 'Aplasia/Hypoplasia of the fovea', 'XPO:0140192', 'abnormally necrotic retina', 0.5058823529411764, 8.040873045973026, 2.0168628550791743, 'HP:0000479', 'Abnormal retinal morphology'),
(404071, 'HP:0008060', 'Aplasia/Hypoplasia of the fovea', 'XPO:0130122', 'increased size of the retinal layer', 0.5058823529411764, 8.040873045973026, 2.0168628550791743, 'HP:0000479', 'Abnormal retinal morphology'),
(404072, 'HP:0008060', 'Aplasia/Hypoplasia of the fovea', 'XPO:0128646', 'decreased size of the outer limiting membrane', 0.4215686274509804, 8.040873045973026, 1.8411354685352277, 'HP:0000479', 'Abnormal retinal morphology'),
(404073, 'HP:0008060', 'Aplasia/Hypoplasia of the fovea', 'XPO:0128787', 'decreased size of the peripheral retina', 0.4725274725274725, 8.040873045973026, 1.9492391893577128, 'HP:0000479', 'Abnormal retinal morphology'),
(404074, 'HP:0008060', 'Aplasia/Hypoplasia of the fovea', 'XPO:0141156', 'abnormally necrotic outer limiting membrane', 0.42574257425742573, 8.040873045973026, 1.850227550835222, 'HP:0000479', 'Abnormal retinal morphology'),
(404075, 'HP:0008060', 'Aplasia/Hypoplasia of the fovea', 'XPO:0140945', 'abnormally necrotic retinal ganglion cell layer', 0.42574257425742573, 8.040873045973026, 1.850227550835222, 'HP:0000479', 'Abnormal retinal morphology'),
(404076, 'HP:0008060', 'Aplasia/Hypoplasia of the fovea', 'XPO:0102441', 'abnormal retinal inner plexiform layer morphology', 0.4574468085106383, 8.040873045973026, 1.9178820903589395, 'HP:0000479', 'Abnormal retinal morphology'),
(404077, 'HP:0008060', 'Aplasia/Hypoplasia of the fovea', 'XPO:0140271', 'abnormally necrotic peripheral retina', 0.48314606741573035, 8.040873045973026, 1.9710190741722953, 'HP:0000479', 'Abnormal retinal morphology'),
(404078, 'HP:0008060', 'Aplasia/Hypoplasia of the fovea', 'XPO:0128884', 'decreased size of the retinal pigmented epithelium', 0.4174757281553398, 8.040873045973026, 1.8321761186829812, 'HP:0000479', 'Abnormal retinal morphology'),
(404079, 'HP:0008060', 'Aplasia/Hypoplasia of the fovea', 'XPO:0102784', 'abnormal retinal progenitor cell region morphology', 0.5119047619047619, 8.040873045973026, 2.028832472656439, 'HP:0000479', 'Abnormal retinal morphology'),
(404080, 'HP:0008060', 'Aplasia/Hypoplasia of the fovea', 'XPO:0128431', 'decreased size of the retinal inner nuclear layer', 0.4215686274509804, 8.040873045973026, 1.8411354685352277, 'HP:0000479', 'Abnormal retinal morphology'),
(404081, 'HP:0008060', 'Aplasia/Hypoplasia of the fovea', 'XPO:0139912', 'abnormally necrotic optic fiber layer', 0.42574257425742573, 8.040873045973026, 1.850227550835222, 'HP:0000479', 'Abnormal retinal morphology'),
(404082, 'HP:0008060', 'Aplasia/Hypoplasia of the fovea', 'XPO:0101861', 'abnormal photoreceptor layer morphology', 0.46236559139784944, 8.040873045973026, 1.9281657141584967, 'HP:0000479', 'Abnormal retinal morphology'),
(404083, 'HP:0008060', 'Aplasia/Hypoplasia of the fovea', 'XPO:0129038', 'decreased size of the retinal outer nuclear layer', 0.4215686274509804, 8.040873045973026, 1.8411354685352277, 'HP:0000479', 'Abnormal retinal morphology'),
(404084, 'HP:0008060', 'Aplasia/Hypoplasia of the fovea', 'XPO:0103926', 'decreased pigmentation in the retinal pigmented epithelium', 0.44329896907216493, 8.040873045973026, 1.8879911895239345, 'HP:0000479', 'Abnormal retinal morphology'),
(404085, 'HP:0008060', 'Aplasia/Hypoplasia of the fovea', 'XPO:0130506', 'increased size of the Muller cell', 0.42574257425742573, 8.040873045973026, 1.850227550835222, 'HP:0000479', 'Abnormal retinal morphology'),
(404086, 'HP:0008060', 'Aplasia/Hypoplasia of the fovea', 'XPO:0128875', 'decreased size of the photoreceptor layer', 0.42574257425742573, 8.040873045973026, 1.850227550835222, 'HP:0000479', 'Abnormal retinal morphology'),
(404087, 'HP:0008060', 'Aplasia/Hypoplasia of the fovea', 'XPO:0130189', 'increased size of the optic chiasm', 0.4019607843137255, 7.796308075334707, 1.7702570741880883, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(404088, 'HP:0008060', 'Aplasia/Hypoplasia of the fovea', 'XPO:0140531', 'abnormally necrotic retinal progenitor cell region', 0.4942528735632184, 8.040873045973026, 1.9935457378573478, 'HP:0000479', 'Abnormal retinal morphology'),
(404089, 'HP:0008060', 'Aplasia/Hypoplasia of the fovea', 'XPO:0130353', 'increased size of the photoreceptor layer', 0.42574257425742573, 8.040873045973026, 1.850227550835222, 'HP:0000479', 'Abnormal retinal morphology'),
(404090, 'HP:0008060', 'Aplasia/Hypoplasia of the fovea', 'XPO:0102239', 'abnormal retinal pigmented epithelium morphology', 0.4574468085106383, 8.040873045973026, 1.9178820903589395, 'HP:0000479', 'Abnormal retinal morphology'),
(404091, 'HP:0008060', 'Aplasia/Hypoplasia of the fovea', 'XPO:0102476', 'abnormal lens transitional zone morphology', 0.40229885057471265, 6.887869297006056, 1.6646266551675757, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(404092, 'HP:0008060', 'Aplasia/Hypoplasia of the fovea', 'XPO:0140439', 'abnormally necrotic retinal stem cell', 0.4387755102040816, 8.040873045973026, 1.8783338822565765, 'HP:0000479', 'Abnormal retinal morphology'),
(404093, 'HP:0008060', 'Aplasia/Hypoplasia of the fovea', 'XPO:0140491', 'abnormally necrotic retinal rod cell', 0.41346153846153844, 8.040873045973026, 1.8233463028623837, 'HP:0000479', 'Abnormal retinal morphology'),
(404094, 'HP:0008060', 'Aplasia/Hypoplasia of the fovea', 'XPO:0128643', 'decreased size of the retinal layer', 0.5058823529411764, 8.040873045973026, 2.0168628550791743, 'HP:0000479', 'Abnormal retinal morphology'),
(404095, 'HP:0008060', 'Aplasia/Hypoplasia of the fovea', 'XPO:0140620', 'abnormally necrotic horizontal cell', 0.4174757281553398, 8.040873045973026, 1.8321761186829812, 'HP:0000479', 'Abnormal retinal morphology'),
(404096, 'HP:0008060', 'Aplasia/Hypoplasia of the fovea', 'XPO:0140218', 'abnormally necrotic sclera', 0.40229885057471265, 6.887869297006056, 1.6646266551675757, 'HP:0012372', 'Abnormal eye morphology'),
(404097, 'HP:0008060', 'Aplasia/Hypoplasia of the fovea', 'XPO:0102162', 'abnormal ciliary marginal zone morphology', 0.48863636363636365, 8.040873045973026, 1.982186410418029, 'HP:0000479', 'Abnormal retinal morphology'),
(404098, 'HP:0008060', 'Aplasia/Hypoplasia of the fovea', 'XPO:0102946', 'abnormal retinal inner nuclear layer morphology', 0.4574468085106383, 8.040873045973026, 1.9178820903589395, 'HP:0000479', 'Abnormal retinal morphology'),
(404099, 'HP:0008060', 'Aplasia/Hypoplasia of the fovea', 'XPO:0129285', 'decreased size of the retinal inner plexiform layer', 0.4215686274509804, 8.040873045973026, 1.8411354685352277, 'HP:0000479', 'Abnormal retinal morphology'),
(404100, 'HP:0008060', 'Aplasia/Hypoplasia of the fovea', 'XPO:0129780', 'increased size of the retina', 0.4942528735632184, 8.040873045973026, 1.9935457378573478, 'HP:0000479', 'Abnormal retinal morphology'),
(404101, 'HP:0008060', 'Aplasia/Hypoplasia of the fovea', 'XPO:0128501', 'decreased size of the retinal ganglion cell layer', 0.4215686274509804, 8.040873045973026, 1.8411354685352277, 'HP:0000479', 'Abnormal retinal morphology'),
(404102, 'HP:0008060', 'Aplasia/Hypoplasia of the fovea', 'XPO:0102815', 'abnormal retinal ganglion cell morphology', 0.43, 8.040873045973026, 1.859455675666511, 'HP:0000479', 'Abnormal retinal morphology'),
(404103, 'HP:0008060', 'Aplasia/Hypoplasia of the fovea', 'XPO:0102581', 'abnormal outer limiting membrane morphology', 0.4574468085106383, 8.040873045973026, 1.9178820903589395, 'HP:0000479', 'Abnormal retinal morphology'),
(404104, 'HP:0008060', 'Aplasia/Hypoplasia of the fovea', 'XPO:0141337', 'increased pigmentation in the eye', 0.4166666666666667, 6.887869297006056, 1.6940913612964297, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(404105, 'HP:0008060', 'Aplasia/Hypoplasia of the fovea', 'XPO:0102196', 'abnormal central retina morphology', 0.5375, 8.040873045973026, 2.0789346459690603, 'HP:0000479', 'Abnormal retinal morphology'),
(404106, 'HP:0008060', 'Aplasia/Hypoplasia of the fovea', 'XPO:0130125', 'increased size of the outer limiting membrane', 0.4215686274509804, 8.040873045973026, 1.8411354685352277, 'HP:0000479', 'Abnormal retinal morphology'),
(404107, 'HP:0008060', 'Aplasia/Hypoplasia of the fovea', 'XPO:0129371', 'decreased size of the retinal outer plexiform layer', 0.4215686274509804, 8.040873045973026, 1.8411354685352277, 'HP:0000479', 'Abnormal retinal morphology'),
(404108, 'HP:0008060', 'Aplasia/Hypoplasia of the fovea', 'XPO:0129775', 'increased size of the retinal neural layer', 0.4215686274509804, 8.040873045973026, 1.8411354685352277, 'HP:0000479', 'Abnormal retinal morphology'),
(404109, 'HP:0008060', 'Aplasia/Hypoplasia of the fovea', 'XPO:0130362', 'increased size of the retinal pigmented epithelium', 0.4174757281553398, 8.040873045973026, 1.8321761186829812, 'HP:0000479', 'Abnormal retinal morphology'),
(404110, 'HP:0008060', 'Aplasia/Hypoplasia of the fovea', 'XPO:0140240', 'abnormally necrotic eye photoreceptor cell', 0.42574257425742573, 8.040873045973026, 1.850227550835222, 'HP:0000479', 'Abnormal retinal morphology'),
(404111, 'HP:0008060', 'Aplasia/Hypoplasia of the fovea', 'XPO:0140006', 'abnormally necrotic retinal neural layer', 0.42574257425742573, 8.040873045973026, 1.850227550835222, 'HP:0000479', 'Abnormal retinal morphology'),
(404112, 'HP:0008060', 'Aplasia/Hypoplasia of the fovea', 'XPO:0102963', 'abnormal retinal outer nuclear layer morphology', 0.4574468085106383, 8.040873045973026, 1.9178820903589395, 'HP:0000479', 'Abnormal retinal morphology'),
(404113, 'HP:0008060', 'Aplasia/Hypoplasia of the fovea', 'XPO:0130257', 'increased size of the retinal blood vessel', 0.4056603773584906, 8.040873045973026, 1.8060630094548564, 'HP:0000479', 'Abnormal retinal morphology'),
(404114, 'HP:0008060', 'Aplasia/Hypoplasia of the fovea', 'XPO:0130845', 'increased size of the retinal outer plexiform layer', 0.4215686274509804, 8.040873045973026, 1.8411354685352277, 'HP:0000479', 'Abnormal retinal morphology'),
(404115, 'HP:0008060', 'Aplasia/Hypoplasia of the fovea', 'XPO:0129981', 'increased size of the retinal ganglion cell layer', 0.4215686274509804, 8.040873045973026, 1.8411354685352277, 'HP:0000479', 'Abnormal retinal morphology'),
(404116, 'HP:0008060', 'Aplasia/Hypoplasia of the fovea', 'XPO:0103186', 'abnormal peripheral retina morphology', 0.5180722891566265, 8.040873045973026, 2.0410177622316423, 'HP:0000479', 'Abnormal retinal morphology'),
(404117, 'HP:0008060', 'Aplasia/Hypoplasia of the fovea', 'XPO:0140317', 'abnormally necrotic retinal progenitor cell', 0.4387755102040816, 8.040873045973026, 1.8783338822565765, 'HP:0000479', 'Abnormal retinal morphology'),
(404118, 'HP:0008060', 'Aplasia/Hypoplasia of the fovea', 'XPO:0129810', 'increased size of the retinal progenitor cell region', 0.48314606741573035, 8.040873045973026, 1.9710190741722953, 'HP:0000479', 'Abnormal retinal morphology'),
(404119, 'HP:0008060', 'Aplasia/Hypoplasia of the fovea', 'XPO:0140464', 'abnormally necrotic retinal pigmented epithelium', 0.4215686274509804, 8.040873045973026, 1.8411354685352277, 'HP:0000479', 'Abnormal retinal morphology'),
(404120, 'HP:0008060', 'Aplasia/Hypoplasia of the fovea', 'XPO:0133369', 'eye fused with brain', 0.4166666666666667, 6.887869297006056, 1.6940913612964297, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(404121, 'HP:0008060', 'Aplasia/Hypoplasia of the fovea', 'XPO:0130413', 'increased size of the central retina', 0.5058823529411764, 8.040873045973026, 2.0168628550791743, 'HP:0000479', 'Abnormal retinal morphology'),
(404122, 'HP:0008060', 'Aplasia/Hypoplasia of the fovea', 'XPO:0133372', 'eye fused with olfactory epithelium', 0.4166666666666667, 6.887869297006056, 1.6940913612964297, 'HP:0012372', 'Abnormal eye morphology'),
(404123, 'HP:0008060', 'Aplasia/Hypoplasia of the fovea', 'XPO:0133371', 'eye fused with olfactory pit', 0.4166666666666667, 6.887869297006056, 1.6940913612964297, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(404124, 'HP:0008060', 'Aplasia/Hypoplasia of the fovea', 'XPO:0129911', 'increased size of the retinal inner nuclear layer', 0.4215686274509804, 8.040873045973026, 1.8411354685352277, 'HP:0000479', 'Abnormal retinal morphology'),
(404125, 'HP:0008060', 'Aplasia/Hypoplasia of the fovea', 'XPO:0141323', 'edematous eye', 0.42168674698795183, 6.887869297006056, 1.7042661756699493, 'HP:0012372', 'Abnormal eye morphology'),
(404126, 'HP:0008060', 'Aplasia/Hypoplasia of the fovea', 'XPO:0102818', 'abnormal optic chiasm morphology', 0.44086021505376344, 7.796308075334707, 1.8539369068869231, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(404127, 'HP:0008060', 'Aplasia/Hypoplasia of the fovea', 'XPO:0102232', 'abnormal eye photoreceptor cell morphology', 0.44329896907216493, 8.040873045973026, 1.8879911895239345, 'HP:0000479', 'Abnormal retinal morphology'),
(404128, 'HP:0008060', 'Aplasia/Hypoplasia of the fovea', 'XPO:0129138', 'decreased size of the retinal progenitor cell', 0.4056603773584906, 8.040873045973026, 1.8060630094548564, 'HP:0000479', 'Abnormal retinal morphology'),
(404129, 'HP:0008060', 'Aplasia/Hypoplasia of the fovea', 'XPO:0128295', 'decreased size of the retinal neural layer', 0.4215686274509804, 8.040873045973026, 1.8411354685352277, 'HP:0000479', 'Abnormal retinal morphology'),
(404130, 'HP:0008060', 'Aplasia/Hypoplasia of the fovea', 'XPO:0102505', 'abnormal retinal stem cell region morphology', 0.5119047619047619, 8.040873045973026, 2.028832472656439, 'HP:0000479', 'Abnormal retinal morphology'),
(404131, 'HP:0008060', 'Aplasia/Hypoplasia of the fovea', 'XPO:0130761', 'increased size of the retinal inner plexiform layer', 0.4215686274509804, 8.040873045973026, 1.8411354685352277, 'HP:0000479', 'Abnormal retinal morphology'),
(404132, 'HP:0008060', 'Aplasia/Hypoplasia of the fovea', 'XPO:0102450', 'abnormal retinal stem cell morphology', 0.46236559139784944, 8.040873045973026, 1.9281657141584967, 'HP:0000479', 'Abnormal retinal morphology'),
(404133, 'HP:0008060', 'Aplasia/Hypoplasia of the fovea', 'XPO:0103155', 'abnormal bipolar neuron morphology', 0.42574257425742573, 8.040873045973026, 1.850227550835222, 'HP:0000479', 'Abnormal retinal morphology'),
(404134, 'HP:0008060', 'Aplasia/Hypoplasia of the fovea', 'XPO:0129029', 'decreased size of the Muller cell', 0.42574257425742573, 8.040873045973026, 1.850227550835222, 'HP:0000479', 'Abnormal retinal morphology'),
(404135, 'HP:0008060', 'Aplasia/Hypoplasia of the fovea', 'XPO:0128669', 'decreased size of the ciliary marginal zone', 0.4387755102040816, 8.040873045973026, 1.8783338822565765, 'HP:0000479', 'Abnormal retinal morphology'),
(404136, 'HP:0008060', 'Aplasia/Hypoplasia of the fovea', 'XPO:0140808', 'abnormally necrotic retinal cone cell', 0.41346153846153844, 8.040873045973026, 1.8233463028623837, 'HP:0000479', 'Abnormal retinal morphology'),
(404137, 'HP:0008060', 'Aplasia/Hypoplasia of the fovea', 'XPO:0139887', 'abnormally necrotic Muller cell', 0.46236559139784944, 8.040873045973026, 1.9281657141584967, 'HP:0000479', 'Abnormal retinal morphology'),
(404138, 'HP:0008060', 'Aplasia/Hypoplasia of the fovea', 'XPO:0128261', 'decreased size of the optic fiber layer', 0.4215686274509804, 8.040873045973026, 1.8411354685352277, 'HP:0000479', 'Abnormal retinal morphology'),
(404139, 'HP:0008060', 'Aplasia/Hypoplasia of the fovea', 'XPO:0140869', 'abnormally necrotic optic chiasm', 0.41836734693877553, 7.796308075334707, 1.8060234564908433, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(404140, 'HP:0008060', 'Aplasia/Hypoplasia of the fovea', 'XPO:0140797', 'abnormally necrotic bipolar neuron', 0.40186915887850466, 8.040873045973026, 1.797603651429875, 'HP:0000479', 'Abnormal retinal morphology'),
(404141, 'HP:0008060', 'Aplasia/Hypoplasia of the fovea', 'XPO:0115423', 'abnormally incomplete structure of eye', 0.4268292682926829, 6.887869297006056, 1.714626551799759, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(404142, 'HP:0008060', 'Aplasia/Hypoplasia of the fovea', 'XPO:0102513', 'abnormal sclera morphology', 0.4268292682926829, 6.887869297006056, 1.714626551799759, 'HP:0012372', 'Abnormal eye morphology'),
(404143, 'HP:0008060', 'Aplasia/Hypoplasia of the fovea', 'XPO:0129580', 'increased size of the inner limiting membrane', 0.4215686274509804, 8.040873045973026, 1.8411354685352277, 'HP:0000479', 'Abnormal retinal morphology'),
(404144, 'HP:0008060', 'Aplasia/Hypoplasia of the fovea', 'XPO:0128475', 'decreased size of the retinal stem cell region', 0.48314606741573035, 8.040873045973026, 1.9710190741722953, 'HP:0000479', 'Abnormal retinal morphology'),
(404145, 'HP:0008060', 'Aplasia/Hypoplasia of the fovea', 'XPO:0102663', 'abnormal retinal progenitor cell morphology', 0.46236559139784944, 8.040873045973026, 1.9281657141584967, 'HP:0000479', 'Abnormal retinal morphology'),
(404146, 'HP:0008060', 'Aplasia/Hypoplasia of the fovea', 'XPO:0103086', 'abnormal amacrine cell morphology', 0.42574257425742573, 8.040873045973026, 1.850227550835222, 'HP:0000479', 'Abnormal retinal morphology'),
(404147, 'HP:0008060', 'Aplasia/Hypoplasia of the fovea', 'XPO:0129955', 'increased size of the retinal stem cell region', 0.48314606741573035, 8.040873045973026, 1.9710190741722953, 'HP:0000479', 'Abnormal retinal morphology'),
(404148, 'HP:0008060', 'Aplasia/Hypoplasia of the fovea', 'XPO:0140391', 'abnormally necrotic central retina', 0.5180722891566265, 8.040873045973026, 2.0410177622316423, 'HP:0000479', 'Abnormal retinal morphology'),
(404149, 'HP:0008060', 'Aplasia/Hypoplasia of the fovea', 'XPO:0127563', 'abnormally localised retinal blood vessel', 0.48314606741573035, 8.040873045973026, 1.9710190741722953, 'HP:0000479', 'Abnormal retinal morphology'),
(404150, 'HP:0008060', 'Aplasia/Hypoplasia of the fovea', 'XPO:0102117', 'abnormal retina morphology', 0.5375, 8.040873045973026, 2.0789346459690603, 'HP:0000479', 'Abnormal retinal morphology'),
(404151, 'HP:0008060', 'Aplasia/Hypoplasia of the fovea', 'XPO:0101817', 'abnormal eye morphology', 0.43209876543209874, 6.887869297006056, 1.7251781994025936, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(404152, 'HP:0008060', 'Aplasia/Hypoplasia of the fovea', 'XPO:0140487', 'abnormally necrotic retinal layer', 0.5119047619047619, 8.040873045973026, 2.028832472656439, 'HP:0000479', 'Abnormal retinal morphology'),
(404153, 'HP:0008060', 'Aplasia/Hypoplasia of the fovea', 'XPO:0102851', 'abnormal retinal rod cell morphology', 0.43434343434343436, 8.040873045973026, 1.8688232698432123, 'HP:0000479', 'Abnormal retinal morphology'),
(404154, 'HP:0008060', 'Aplasia/Hypoplasia of the fovea', 'XPO:0102017', 'abnormal retinal neural layer morphology', 0.46236559139784944, 8.040873045973026, 1.9281657141584967, 'HP:0000479', 'Abnormal retinal morphology'),
(404155, 'HP:0008060', 'Aplasia/Hypoplasia of the fovea', 'XPO:0140671', 'abnormally necrotic retinal ganglion cell', 0.4095238095238095, 8.040873045973026, 1.8146429295275122, 'HP:0000479', 'Abnormal retinal morphology'),
(404156, 'HP:0008060', 'Aplasia/Hypoplasia of the fovea', 'XPO:0141638', 'neoplastic eye', 0.4166666666666667, 6.887869297006056, 1.6940913612964297, 'HP:0012372', 'Abnormal eye morphology'),
(404157, 'HP:0008060', 'Aplasia/Hypoplasia of the fovea', 'XPO:0130906', 'increased size of the retinal stem cell', 0.4056603773584906, 8.040873045973026, 1.8060630094548564, 'HP:0000479', 'Abnormal retinal morphology'),
(404158, 'HP:0008060', 'Aplasia/Hypoplasia of the fovea', 'XPO:0100329', 'abnormal retinal blood vessel', 0.5443037974683544, 8.040873045973026, 2.0920510830006163, 'HP:0000479', 'Abnormal retinal morphology'),
(404159, 'HP:0008060', 'Aplasia/Hypoplasia of the fovea', 'XPO:0102550', 'abnormal lens morphology', 0.4117647058823529, 6.887869297006056, 1.6840966347682629, 'HP:0012372', 'Abnormal eye morphology'),
(404160, 'HP:0008060', 'Aplasia/Hypoplasia of the fovea', 'XPO:0129741', 'increased size of the optic fiber layer', 0.4215686274509804, 8.040873045973026, 1.8411354685352277, 'HP:0000479', 'Abnormal retinal morphology'),
(404161, 'HP:0008060', 'Aplasia/Hypoplasia of the fovea', 'XPO:0100371', 'abnormal hyaloid blood vessel', 0.4025974025974026, 6.887869297006056, 1.6652442128423794, 'HP:0012372', 'Abnormal eye morphology'),
(404162, 'HP:0008060', 'Aplasia/Hypoplasia of the fovea', 'XPO:0141014', 'abnormally necrotic retinal outer plexiform layer', 0.42574257425742573, 8.040873045973026, 1.850227550835222, 'HP:0000479', 'Abnormal retinal morphology'),
(404163, 'HP:0008060', 'Aplasia/Hypoplasia of the fovea', 'XPO:0141033', 'abnormally necrotic photoreceptor layer', 0.43, 8.040873045973026, 1.859455675666511, 'HP:0000479', 'Abnormal retinal morphology'),
(404164, 'HP:0008060', 'Aplasia/Hypoplasia of the fovea', 'XPO:0130515', 'increased size of the retinal outer nuclear layer', 0.4215686274509804, 8.040873045973026, 1.8411354685352277, 'HP:0000479', 'Abnormal retinal morphology'),
(404165, 'HP:0008060', 'Aplasia/Hypoplasia of the fovea', 'XPO:0130614', 'increased size of the retinal progenitor cell', 0.4056603773584906, 8.040873045973026, 1.8060630094548564, 'HP:0000479', 'Abnormal retinal morphology'),
(404166, 'HP:0008060', 'Aplasia/Hypoplasia of the fovea', 'XPO:0101961', 'abnormal retinal blood vessel morphology', 0.44329896907216493, 8.040873045973026, 1.8879911895239345, 'HP:0000479', 'Abnormal retinal morphology'),
(404167, 'HP:0008060', 'Aplasia/Hypoplasia of the fovea', 'XPO:0140489', 'abnormally necrotic ciliary marginal zone', 0.4479166666666667, 8.040873045973026, 1.8977990019604511, 'HP:0000479', 'Abnormal retinal morphology'),
(404168, 'HP:0008060', 'Aplasia/Hypoplasia of the fovea', 'XPO:0129432', 'decreased size of the retinal stem cell', 0.4056603773584906, 8.040873045973026, 1.8060630094548564, 'HP:0000479', 'Abnormal retinal morphology'),
(404169, 'HP:0008060', 'Aplasia/Hypoplasia of the fovea', 'XPO:0102882', 'abnormal retinal cone cell morphology', 0.43434343434343436, 8.040873045973026, 1.8688232698432123, 'HP:0000479', 'Abnormal retinal morphology'),
(404170, 'HP:0008060', 'Aplasia/Hypoplasia of the fovea', 'XPO:0128710', 'decreased size of the optic chiasm', 0.4019607843137255, 7.796308075334707, 1.7702570741880883, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(404171, 'HP:0008060', 'Aplasia/Hypoplasia of the fovea', 'XPO:0102266', 'abnormal horizontal cell morphology', 0.4387755102040816, 8.040873045973026, 1.8783338822565765, 'HP:0000479', 'Abnormal retinal morphology'),
(404172, 'HP:0033251', 'Elevated residual volume', 'XPO:0101543', 'abnormal external gill', 0.41935483870967744, 6.780552239366747, 1.6862554345953, 'UPHENO:0004536', 'abnormal respiratory system'),
(404173, 'HP:0033251', 'Elevated residual volume', 'XPO:0100317', 'abnormal respiratory system', 0.48148148148148145, 6.780552239366747, 1.8068509450070522, 'UPHENO:0004536', 'abnormal respiratory system'),
(404174, 'HP:0033251', 'Elevated residual volume', 'XPO:0100804', 'abnormal larynx', 0.42857142857142855, 7.032762738978795, 1.7360994135843877, 'UPHENO:0002448', 'abnormality of respiratory system physiology'),
(404175, 'HP:0033251', 'Elevated residual volume', 'XPO:0130015', 'increased size of the respiratory system', 0.4090909090909091, 7.032762738978795, 1.6961837466234333, 'UPHENO:0002448', 'abnormality of respiratory system physiology'),
(404176, 'HP:0033251', 'Elevated residual volume', 'XPO:0101949', 'abnormal respiratory system morphology', 0.4864864864864865, 7.032762738978795, 1.8496875506903518, 'HP:0002795', 'Abnormal respiratory system physiology'),
(404177, 'HP:0033251', 'Elevated residual volume', 'XPO:0139850', 'abnormally necrotic respiratory system', 0.42857142857142855, 7.032762738978795, 1.7360994135843877, 'HP:0002795', 'Abnormal respiratory system physiology'),
(404178, 'HP:0033251', 'Elevated residual volume', 'XPO:0100004', 'abnormal cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(404179, 'HP:0033251', 'Elevated residual volume', 'XPO:0128535', 'decreased size of the respiratory system', 0.4090909090909091, 7.032762738978795, 1.6961837466234333, 'UPHENO:0002448', 'abnormality of respiratory system physiology'),
(404180, 'HP:0100751', 'Esophageal neoplasm', 'XPO:0100523', 'abnormal midgut', 0.40540540540540543, 5.05060299610679, 1.4309233924911664, 'HP:0025031', 'Abnormality of the digestive system'),
(404181, 'HP:0100751', 'Esophageal neoplasm', 'XPO:0107375', 'abnormal larval alimentary system morphology', 0.4186046511627907, 5.725717590856133, 1.5481640787645816, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(404182, 'HP:0100751', 'Esophageal neoplasm', 'XPO:0101377', 'abnormal manicotto glandulare', 0.40540540540540543, 5.05060299610679, 1.4309233924911664, 'HP:0025031', 'Abnormality of the digestive system'),
(404183, 'HP:0100751', 'Esophageal neoplasm', 'XPO:0141819', 'neoplastic esophagus', 0.42857142857142855, 11.61213700143767, 2.23083619826138, 'UPHENO:0076752', 'abnormal esophagus morphology'),
(404184, 'HP:0100751', 'Esophageal neoplasm', 'XPO:0100890', 'abnormal pharyngeal cavity', 0.4166666666666667, 5.05060299610679, 1.45066119926208, 'HP:0025031', 'Abnormality of the digestive system'),
(404185, 'HP:0100751', 'Esophageal neoplasm', 'XPO:0115391', 'abnormally undifferentiated alimentary system', 0.42857142857142855, 5.05060299610679, 1.471238981671103, 'HP:0025031', 'Abnormality of the digestive system'),
(404186, 'HP:0100751', 'Esophageal neoplasm', 'XPO:0101306', 'abnormal ileum', 0.4230769230769231, 8.037124161124119, 1.8439961389535469, 'UPHENO:0076735', 'abnormal alimentary part of gastrointestinal system morphology'),
(404187, 'HP:0100751', 'Esophageal neoplasm', 'XPO:0102429', 'abnormal esophagus morphology', 0.4444444444444444, 11.61213700143767, 2.2717723870178417, 'UPHENO:0076752', 'abnormal esophagus morphology'),
(404188, 'HP:0100751', 'Esophageal neoplasm', 'XPO:0142054', 'abnormal digestive tract', 0.4166666666666667, 5.05060299610679, 1.45066119926208, 'HP:0025031', 'Abnormality of the digestive system'),
(404189, 'HP:0100751', 'Esophageal neoplasm', 'XPO:0107288', 'abnormal larval alimentary system', 0.42857142857142855, 5.05060299610679, 1.471238981671103, 'HP:0025031', 'Abnormality of the digestive system'),
(404190, 'HP:0100751', 'Esophageal neoplasm', 'XPO:0141308', 'abnormal esophageal epithelium morphology', 0.41379310344827586, 11.61213700143767, 2.1920360871781854, 'UPHENO:0076752', 'abnormal esophagus morphology'),
(404191, 'HP:0100751', 'Esophageal neoplasm', 'XPO:0101537', 'abnormal internal coil of the small intestine', 0.4230769230769231, 8.037124161124119, 1.8439961389535469, 'UPHENO:0076735', 'abnormal alimentary part of gastrointestinal system morphology'),
(404192, 'HP:0100751', 'Esophageal neoplasm', 'XPO:0102522', 'abnormal pharyngeal cavity morphology', 0.43902439024390244, 5.725717590856133, 1.5854745895265556, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(404193, 'HP:0100751', 'Esophageal neoplasm', 'XPO:0100152', 'abnormal alimentary system', 0.4411764705882353, 5.05060299610679, 1.4927180591674907, 'HP:0025031', 'Abnormality of the digestive system'),
(404194, 'HP:0100751', 'Esophageal neoplasm', 'XPO:0101784', 'abnormal alimentary system morphology', 0.43902439024390244, 5.725717590856133, 1.5854745895265556, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(404195, 'HP:0100751', 'Esophageal neoplasm', 'XPO:0100486', 'abnormal oral evagination', 0.40540540540540543, 5.05060299610679, 1.4309233924911664, 'HP:0025031', 'Abnormality of the digestive system'),
(404196, 'HP:0100751', 'Esophageal neoplasm', 'XPO:0102125', 'abnormal liver and biliary system morphology', 0.4186046511627907, 5.725717590856133, 1.5481640787645816, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(404197, 'HP:0100751', 'Esophageal neoplasm', 'XPO:0115392', 'abnormally incomplete structure of alimentary system', 0.42857142857142855, 5.725717590856133, 1.5664861849086864, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(404198, 'HP:0100751', 'Esophageal neoplasm', 'XPO:0142061', 'abnormal digestive tract morphology', 0.4186046511627907, 5.725717590856133, 1.5481640787645816, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(404199, 'HP:0100751', 'Esophageal neoplasm', 'XPO:0102118', 'abnormal oral evagination morphology', 0.4090909090909091, 5.725717590856133, 1.5304701939081158, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(404200, 'HP:0100751', 'Esophageal neoplasm', 'XPO:0101321', 'abnormal duodenum', 0.4230769230769231, 8.037124161124119, 1.8439961389535469, 'UPHENO:0076735', 'abnormal alimentary part of gastrointestinal system morphology'),
(404201, 'HP:0100751', 'Esophageal neoplasm', 'XPO:0100493', 'abnormal liver and biliary system', 0.42857142857142855, 5.05060299610679, 1.471238981671103, 'HP:0025031', 'Abnormality of the digestive system'),
(404202, 'HP:0100751', 'Esophageal neoplasm', 'XPO:0100361', 'abnormal small intestine', 0.43137254901960786, 8.037124161124119, 1.861986771212725, 'UPHENO:0076735', 'abnormal alimentary part of gastrointestinal system morphology'),
(404203, 'HP:0100751', 'Esophageal neoplasm', 'XPO:0141833', 'edematous alimentary system', 0.4186046511627907, 5.725717590856133, 1.5481640787645816, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(404204, 'HP:0100751', 'Esophageal neoplasm', 'XPO:0100156', 'abnormal foregut', 0.40540540540540543, 5.05060299610679, 1.4309233924911664, 'HP:0025031', 'Abnormality of the digestive system'),
(404205, 'HP:0100751', 'Esophageal neoplasm', 'XPO:0103009', 'abnormal manicotto glandulare morphology', 0.4090909090909091, 5.725717590856133, 1.5304701939081158, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(404206, 'HP:0100751', 'Esophageal neoplasm', 'XPO:0133434', 'abnormal cilium morphology in the esophagus', 0.41379310344827586, 11.61213700143767, 2.1920360871781854, 'UPHENO:0076752', 'abnormal esophagus morphology'),
(404207, 'HP:0100751', 'Esophageal neoplasm', 'XPO:0101288', 'abnormal external coil of the small intestine', 0.4230769230769231, 8.037124161124119, 1.8439961389535469, 'UPHENO:0076735', 'abnormal alimentary part of gastrointestinal system morphology'),
(404208, 'HP:0100751', 'Esophageal neoplasm', 'XPO:0100735', 'abnormal hindgut', 0.40540540540540543, 5.05060299610679, 1.4309233924911664, 'HP:0025031', 'Abnormality of the digestive system'),
(404209, 'HP:0001355', 'Megalencephaly', 'XPO:0128277', 'decreased size of the striatum', 0.4264705882352941, 8.02346099791745, 1.8498027277157947, 'HP:0002060', 'Abnormal cerebral morphology'),
(404210, 'HP:0001355', 'Megalencephaly', 'XPO:0129962', 'increased size of the ventral pallium', 0.4393939393939394, 8.02346099791745, 1.8776208710622537, 'HP:0002060', 'Abnormal cerebral morphology'),
(404211, 'HP:0001355', 'Megalencephaly', 'XPO:0100971', 'abnormal prethalamus basal plate', 0.47368421052631576, 6.667568321314008, 1.7771668003909757, 'HP:0100547', 'Abnormal forebrain morphology'),
(404212, 'HP:0001355', 'Megalencephaly', 'XPO:0102395', 'abnormal pretectum morphology', 0.43548387096774194, 6.667568321314008, 1.704000722566664, 'HP:0100547', 'Abnormal forebrain morphology'),
(404213, 'HP:0001355', 'Megalencephaly', 'XPO:0129951', 'increased size of the anterior amygdala', 0.4084507042253521, 8.02346099791745, 1.810300608993995, 'HP:0002060', 'Abnormal cerebral morphology'),
(404214, 'HP:0001355', 'Megalencephaly', 'XPO:0140021', 'abnormally necrotic striatum', 0.4393939393939394, 8.02346099791745, 1.8776208710622537, 'HP:0002060', 'Abnormal cerebral morphology'),
(404215, 'HP:0001355', 'Megalencephaly', 'XPO:0102968', 'abnormal medial ganglionic eminence morphology', 0.48333333333333334, 8.02346099791745, 1.969265383079039, 'HP:0002060', 'Abnormal cerebral morphology'),
(404216, 'HP:0001355', 'Megalencephaly', 'XPO:0103220', 'abnormal central nucleus of the thalamus morphology', 0.4153846153846154, 6.667568321314008, 1.6642131181731699, 'HP:0100547', 'Abnormal forebrain morphology'),
(404217, 'HP:0001355', 'Megalencephaly', 'XPO:0101862', 'abnormal brain ventricle morphology', 0.43636363636363634, 6.005340694266148, 1.618799648799227, 'UPHENO:0081435', 'abnormal anatomical entity morphology in the brain'),
(404218, 'HP:0001355', 'Megalencephaly', 'XPO:0131746', 'abnormal neural tube closure', 0.4666666666666667, 5.483278994082134, 1.5996448138795258, 'HP:0002011', 'Morphological central nervous system abnormality'),
(404219, 'HP:0001355', 'Megalencephaly', 'XPO:0130936', 'increased size of the medial septum', 0.4084507042253521, 8.02346099791745, 1.810300608993995, 'HP:0002060', 'Abnormal cerebral morphology'),
(404220, 'HP:0001355', 'Megalencephaly', 'XPO:0129908', 'increased size of the ventral pallidum', 0.42028985507246375, 8.02346099791745, 1.8363494384224073, 'HP:0002060', 'Abnormal cerebral morphology'),
(404221, 'HP:0001355', 'Megalencephaly', 'XPO:0102169', 'abnormal medium cavity morphology', 0.4418604651162791, 4.7814666189787065, 1.4535271116150168, 'HP:0012639', 'Abnormal nervous system morphology'),
(404222, 'HP:0001355', 'Megalencephaly', 'XPO:0100946', 'abnormal melanotrope', 0.45, 6.667568321314008, 1.7321679319833003, 'HP:0100547', 'Abnormal forebrain morphology'),
(404223, 'HP:0001355', 'Megalencephaly', 'XPO:0102105', 'abnormal ventral habenular nucleus morphology', 0.40298507462686567, 6.667568321314008, 1.639185931352649, 'HP:0100547', 'Abnormal forebrain morphology'),
(404224, 'HP:0001355', 'Megalencephaly', 'XPO:0101595', 'abnormal prosomere 4', 0.48214285714285715, 6.667568321314008, 1.7929641492884176, 'HP:0100547', 'Abnormal forebrain morphology'),
(404225, 'HP:0001355', 'Megalencephaly', 'XPO:0141149', 'abnormally necrotic dorsal pallium', 0.453125, 8.02346099791745, 1.9067330082319718, 'HP:0002060', 'Abnormal cerebral morphology'),
(404226, 'HP:0001355', 'Megalencephaly', 'XPO:0130873', 'increased size of the medial pallium', 0.4393939393939394, 8.02346099791745, 1.8776208710622537, 'HP:0002060', 'Abnormal cerebral morphology'),
(404227, 'HP:0001355', 'Megalencephaly', 'XPO:0140574', 'abnormally necrotic medial ganglionic eminence', 0.4461538461538462, 8.02346099791745, 1.8920089808682852, 'HP:0002060', 'Abnormal cerebral morphology'),
(404228, 'HP:0001355', 'Megalencephaly', 'XPO:0101184', 'abnormal suprachiasmatic nucleus', 0.46551724137931033, 6.667568321314008, 1.7617797852303152, 'HP:0100547', 'Abnormal forebrain morphology'),
(404229, 'HP:0001355', 'Megalencephaly', 'XPO:0141259', 'abnormally necrotic accessory olfactory bulb', 0.4142857142857143, 8.02346099791745, 1.8231854734408677, 'HP:0002060', 'Abnormal cerebral morphology'),
(404230, 'HP:0001355', 'Megalencephaly', 'XPO:0130557', 'increased size of the medial ganglionic eminence', 0.43283582089552236, 8.02346099791745, 1.8635560972122107, 'HP:0002060', 'Abnormal cerebral morphology'),
(404231, 'HP:0001355', 'Megalencephaly', 'XPO:0101825', 'abnormal granule cell layer of the olfactory bulb morphology', 0.4393939393939394, 8.02346099791745, 1.8776208710622537, 'HP:0002060', 'Abnormal cerebral morphology'),
(404232, 'HP:0001355', 'Megalencephaly', 'XPO:0102603', 'abnormal prethalamus basal plate morphology', 0.421875, 6.667568321314008, 1.677164388351466, 'HP:0100547', 'Abnormal forebrain morphology'),
(404233, 'HP:0001355', 'Megalencephaly', 'XPO:0102760', 'abnormal dorsal pallidum morphology', 0.46774193548387094, 8.02346099791745, 1.9372426736073256, 'HP:0002060', 'Abnormal cerebral morphology'),
(404234, 'HP:0001355', 'Megalencephaly', 'XPO:0101987', 'abnormal striatum morphology', 0.47540983606557374, 8.02346099791745, 1.9530571619126922, 'HP:0002060', 'Abnormal cerebral morphology'),
(404235, 'HP:0001355', 'Megalencephaly', 'XPO:0102281', 'abnormal growth cone morphology', 0.41304347826086957, 4.7814666189787065, 1.405330425021534, 'HP:0012639', 'Abnormal nervous system morphology'),
(404236, 'HP:0001355', 'Megalencephaly', 'XPO:0101851', 'abnormal basal ganglion morphology', 0.48333333333333334, 8.02346099791745, 1.969265383079039, 'HP:0002060', 'Abnormal cerebral morphology'),
(404237, 'HP:0001355', 'Megalencephaly', 'XPO:0127050', 'abnormally localised adenohypophysis', 0.4153846153846154, 6.667568321314008, 1.6642131181731699, 'HP:0100547', 'Abnormal forebrain morphology'),
(404238, 'HP:0001355', 'Megalencephaly', 'XPO:0129196', 'decreased size of the dorsal pallidum', 0.42028985507246375, 8.02346099791745, 1.8363494384224073, 'HP:0002060', 'Abnormal cerebral morphology'),
(404239, 'HP:0001355', 'Megalencephaly', 'XPO:0102584', 'abnormal dorsal septum morphology', 0.4603174603174603, 8.02346099791745, 1.9218062310018553, 'HP:0002060', 'Abnormal cerebral morphology'),
(404240, 'HP:0001355', 'Megalencephaly', 'XPO:0103230', 'abnormal left ventricle morphology', 0.4067796610169492, 6.005340694266148, 1.562962076284922, 'UPHENO:0081435', 'abnormal anatomical entity morphology in the brain'),
(404241, 'HP:0001355', 'Megalencephaly', 'XPO:0127143', 'abnormally localised thalamus', 0.43548387096774194, 6.667568321314008, 1.704000722566664, 'HP:0100547', 'Abnormal forebrain morphology'),
(404242, 'HP:0001355', 'Megalencephaly', 'XPO:0126680', 'abnormally localised tuberal region', 0.421875, 6.667568321314008, 1.677164388351466, 'HP:0100547', 'Abnormal forebrain morphology'),
(404243, 'HP:0001355', 'Megalencephaly', 'XPO:0100590', 'abnormal hypothalamus', 0.5, 6.667568321314008, 1.825865318323617, 'HP:0100547', 'Abnormal forebrain morphology'),
(404244, 'HP:0001355', 'Megalencephaly', 'XPO:0128459', 'decreased size of the prosomere 6', 0.4084507042253521, 8.02346099791745, 1.810300608993995, 'HP:0002060', 'Abnormal cerebral morphology'),
(404245, 'HP:0001355', 'Megalencephaly', 'XPO:0101789', 'abnormal optic tract morphology', 0.421875, 6.667568321314008, 1.677164388351466, 'HP:0100547', 'Abnormal forebrain morphology'),
(404246, 'HP:0001355', 'Megalencephaly', 'XPO:0102222', 'abnormal hypothalamus morphology', 0.4153846153846154, 6.667568321314008, 1.6642131181731699, 'HP:0100547', 'Abnormal forebrain morphology'),
(404247, 'HP:0001355', 'Megalencephaly', 'XPO:0103178', 'abnormal dorsal pallium morphology', 0.4915254237288136, 8.02346099791745, 1.9858839509832855, 'HP:0002060', 'Abnormal cerebral morphology'),
(404248, 'HP:0001355', 'Megalencephaly', 'XPO:0100157', 'abnormal optic tract', 0.5, 6.667568321314008, 1.825865318323617, 'HP:0100547', 'Abnormal forebrain morphology'),
(404249, 'HP:0001355', 'Megalencephaly', 'XPO:0100656', 'abnormal ventral hypothalamic nucleus', 0.47368421052631576, 6.667568321314008, 1.7771668003909757, 'HP:0100547', 'Abnormal forebrain morphology'),
(404250, 'HP:0001355', 'Megalencephaly', 'XPO:0129469', 'decreased size of the anterior entopeduncular nucleus', 0.4027777777777778, 8.02346099791745, 1.7976851200440698, 'HP:0002060', 'Abnormal cerebral morphology'),
(404251, 'HP:0001355', 'Megalencephaly', 'XPO:0101805', 'abnormal pallidum morphology', 0.47540983606557374, 8.02346099791745, 1.9530571619126922, 'HP:0002060', 'Abnormal cerebral morphology'),
(404252, 'HP:0001355', 'Megalencephaly', 'XPO:0103102', 'abnormal anterior amygdala morphology', 0.4603174603174603, 8.02346099791745, 1.9218062310018553, 'HP:0002060', 'Abnormal cerebral morphology'),
(404253, 'HP:0001355', 'Megalencephaly', 'XPO:0129739', 'increased size of the nervous system', 0.40425531914893614, 4.7814666189787065, 1.3902997209433732, 'HP:0012639', 'Abnormal nervous system morphology'),
(404254, 'HP:0001355', 'Megalencephaly', 'XPO:0128708', 'decreased size of the basal forebrain', 0.4461538461538462, 8.02346099791745, 1.8920089808682852, 'HP:0002060', 'Abnormal cerebral morphology'),
(404255, 'HP:0001355', 'Megalencephaly', 'XPO:0101827', 'abnormal retromammillary area morphology', 0.421875, 6.667568321314008, 1.677164388351466, 'HP:0100547', 'Abnormal forebrain morphology'),
(404256, 'HP:0001355', 'Megalencephaly', 'XPO:0139760', 'abnormally necrotic basal ganglion', 0.4461538461538462, 8.02346099791745, 1.8920089808682852, 'HP:0002060', 'Abnormal cerebral morphology'),
(404257, 'HP:0001355', 'Megalencephaly', 'XPO:0139876', 'abnormally necrotic mitral cell layer of the olfactory bulb', 0.4084507042253521, 8.02346099791745, 1.810300608993995, 'HP:0002060', 'Abnormal cerebral morphology'),
(404258, 'HP:0001355', 'Megalencephaly', 'XPO:0102983', 'abnormal dorsal habenular nucleus morphology', 0.40298507462686567, 6.667568321314008, 1.639185931352649, 'HP:0100547', 'Abnormal forebrain morphology'),
(404259, 'HP:0001355', 'Megalencephaly', 'XPO:0140186', 'abnormally necrotic pallium', 0.4603174603174603, 8.02346099791745, 1.9218062310018553, 'HP:0002060', 'Abnormal cerebral morphology'),
(404260, 'HP:0001355', 'Megalencephaly', 'XPO:0100304', 'abnormal medulla oblongata', 0.41379310344827586, 6.005340694266148, 1.5763783058468588, 'UPHENO:0081435', 'abnormal anatomical entity morphology in the brain'),
(404261, 'HP:0001355', 'Megalencephaly', 'XPO:0102892', 'abnormal central canal morphology', 0.42, 5.483278994082134, 1.5175563177406288, 'HP:0002011', 'Morphological central nervous system abnormality'),
(404262, 'HP:0001355', 'Megalencephaly', 'XPO:0128602', 'decreased size of the subpallium', 0.4461538461538462, 8.02346099791745, 1.8920089808682852, 'HP:0002060', 'Abnormal cerebral morphology'),
(404263, 'HP:0001355', 'Megalencephaly', 'XPO:0128444', 'decreased size of the telencephalon', 0.453125, 8.02346099791745, 1.9067330082319718, 'HP:0002060', 'Abnormal cerebral morphology'),
(404264, 'HP:0001355', 'Megalencephaly', 'XPO:0102951', 'abnormal lateral amygdala morphology', 0.4603174603174603, 8.02346099791745, 1.9218062310018553, 'HP:0002060', 'Abnormal cerebral morphology'),
(404265, 'HP:0001355', 'Megalencephaly', 'XPO:0102274', 'abnormal gustatory system morphology', 0.4318181818181818, 4.7814666189787065, 1.4369148276191301, 'HP:0012639', 'Abnormal nervous system morphology'),
(404266, 'HP:0001355', 'Megalencephaly', 'XPO:0129757', 'increased size of the striatum', 0.4264705882352941, 8.02346099791745, 1.8498027277157947, 'HP:0002060', 'Abnormal cerebral morphology'),
(404267, 'HP:0001355', 'Megalencephaly', 'XPO:0127764', 'abnormally localised optic chiasm', 0.43548387096774194, 6.667568321314008, 1.704000722566664, 'HP:0100547', 'Abnormal forebrain morphology'),
(404268, 'HP:0001355', 'Megalencephaly', 'XPO:0102234', 'abnormal right ventricle morphology', 0.4067796610169492, 6.005340694266148, 1.562962076284922, 'UPHENO:0081435', 'abnormal anatomical entity morphology in the brain'),
(404269, 'HP:0001355', 'Megalencephaly', 'XPO:0139738', 'abnormally necrotic olfactory bulb', 0.4084507042253521, 8.02346099791745, 1.810300608993995, 'HP:0002060', 'Abnormal cerebral morphology'),
(404270, 'HP:0001355', 'Megalencephaly', 'XPO:0100962', 'abnormal dorsal thalamus', 0.4909090909090909, 6.667568321314008, 1.8091903999276895, 'HP:0100547', 'Abnormal forebrain morphology'),
(404271, 'HP:0001355', 'Megalencephaly', 'XPO:0101117', 'abnormal tuberal region', 0.48214285714285715, 6.667568321314008, 1.7929641492884176, 'HP:0100547', 'Abnormal forebrain morphology'),
(404272, 'HP:0001355', 'Megalencephaly', 'XPO:0126877', 'abnormally localised diencephalon', 0.4426229508196721, 6.667568321314008, 1.7179111633526845, 'HP:0100547', 'Abnormal forebrain morphology'),
(404273, 'HP:0001355', 'Megalencephaly', 'XPO:0130183', 'increased size of the lateral pallium', 0.4393939393939394, 8.02346099791745, 1.8776208710622537, 'HP:0002060', 'Abnormal cerebral morphology'),
(404274, 'HP:0001355', 'Megalencephaly', 'XPO:0101354', 'abnormal eminentia thalami', 0.5, 6.667568321314008, 1.825865318323617, 'HP:0100547', 'Abnormal forebrain morphology'),
(404275, 'HP:0001355', 'Megalencephaly', 'XPO:0102490', 'abnormal presumptive midbrain-hindbrain boundary morphology', 0.45652173913043476, 5.483278994082134, 1.5821618319614958, 'HP:0002011', 'Morphological central nervous system abnormality'),
(404276, 'HP:0001355', 'Megalencephaly', 'XPO:0100575', 'abnormal diencephalon', 0.5094339622641509, 6.667568321314008, 1.8430099697489237, 'HP:0100547', 'Abnormal forebrain morphology'),
(404277, 'HP:0001355', 'Megalencephaly', 'XPO:0101652', 'abnormal external plexiform layer of the olfactory bulb morphology', 0.4393939393939394, 8.02346099791745, 1.8776208710622537, 'HP:0002060', 'Abnormal cerebral morphology'),
(404278, 'HP:0001355', 'Megalencephaly', 'XPO:0128187', 'decreased size of the basal ganglion', 0.43283582089552236, 8.02346099791745, 1.8635560972122107, 'HP:0002060', 'Abnormal cerebral morphology'),
(404279, 'HP:0001355', 'Megalencephaly', 'XPO:0140023', 'abnormally necrotic thalamus', 0.4090909090909091, 6.667568321314008, 1.6515573214369805, 'HP:0100547', 'Abnormal forebrain morphology'),
(404280, 'HP:0001355', 'Megalencephaly', 'XPO:0141304', 'abnormal pia mater morphology', 0.42105263157894735, 6.005340694266148, 1.590146063369307, 'UPHENO:0081435', 'abnormal anatomical entity morphology in the brain'),
(404281, 'HP:0001355', 'Megalencephaly', 'XPO:0101802', 'abnormal anterior neural tube morphology', 0.42, 5.483278994082134, 1.5175563177406288, 'HP:0002011', 'Morphological central nervous system abnormality'),
(404282, 'HP:0001355', 'Megalencephaly', 'XPO:0100951', 'abnormal adenohypophysis', 0.47368421052631576, 6.667568321314008, 1.7771668003909757, 'HP:0100547', 'Abnormal forebrain morphology'),
(404283, 'HP:0001355', 'Megalencephaly', 'XPO:0102007', 'abnormal anterior entopeduncular region morphology', 0.5178571428571429, 8.02346099791745, 2.038383327101959, 'HP:0002060', 'Abnormal cerebral morphology'),
(404284, 'HP:0001355', 'Megalencephaly', 'XPO:0103227', 'abnormal prosomere 4 morphology', 0.4153846153846154, 6.667568321314008, 1.6642131181731699, 'HP:0100547', 'Abnormal forebrain morphology'),
(404285, 'HP:0001355', 'Megalencephaly', 'XPO:0101284', 'abnormal ventromedial thalamic nucleus', 0.47368421052631576, 6.667568321314008, 1.7771668003909757, 'HP:0100547', 'Abnormal forebrain morphology'),
(404286, 'HP:0001355', 'Megalencephaly', 'XPO:0103144', 'abnormal lateral funiculus morphology', 0.42, 5.483278994082134, 1.5175563177406288, 'HP:0002011', 'Morphological central nervous system abnormality'),
(404287, 'HP:0001355', 'Megalencephaly', 'XPO:0128259', 'decreased size of the nervous system', 0.40425531914893614, 4.7814666189787065, 1.3902997209433732, 'HP:0012639', 'Abnormal nervous system morphology'),
(404288, 'HP:0001355', 'Megalencephaly', 'XPO:0103025', 'abnormal dorsolateral neural tube morphology', 0.42, 5.483278994082134, 1.5175563177406288, 'HP:0002011', 'Morphological central nervous system abnormality'),
(404289, 'HP:0001355', 'Megalencephaly', 'XPO:0100611', 'abnormal hypophysis', 0.48214285714285715, 6.667568321314008, 1.7929641492884176, 'HP:0100547', 'Abnormal forebrain morphology'),
(404290, 'HP:0001355', 'Megalencephaly', 'XPO:0130228', 'increased size of the ventricular zone', 0.4067796610169492, 6.005340694266148, 1.562962076284922, 'UPHENO:0081435', 'abnormal anatomical entity morphology in the brain'),
(404291, 'HP:0001355', 'Megalencephaly', 'XPO:0103075', 'abnormal subthalamic nucleus morphology', 0.42028985507246375, 8.02346099791745, 1.8363494384224073, 'HP:0002060', 'Abnormal cerebral morphology'),
(404292, 'HP:0001355', 'Megalencephaly', 'XPO:0141504', 'abnormal axon microtubule bundle morphology', 0.40425531914893614, 4.7814666189787065, 1.3902997209433732, 'HP:0012639', 'Abnormal nervous system morphology'),
(404293, 'HP:0001355', 'Megalencephaly', 'XPO:0102509', 'abnormal lateral septum morphology', 0.4603174603174603, 8.02346099791745, 1.9218062310018553, 'HP:0002060', 'Abnormal cerebral morphology'),
(404294, 'HP:0001355', 'Megalencephaly', 'XPO:0102620', 'abnormal habenula morphology', 0.42857142857142855, 6.667568321314008, 1.6904228111816126, 'HP:0100547', 'Abnormal forebrain morphology'),
(404295, 'HP:0001355', 'Megalencephaly', 'XPO:0103107', 'abnormal ventral septum morphology', 0.4603174603174603, 8.02346099791745, 1.9218062310018553, 'HP:0002060', 'Abnormal cerebral morphology'),
(404296, 'HP:0001355', 'Megalencephaly', 'XPO:0102059', 'abnormal olfactory system morphology', 0.4318181818181818, 4.7814666189787065, 1.4369148276191301, 'HP:0012639', 'Abnormal nervous system morphology'),
(404297, 'HP:0001355', 'Megalencephaly', 'XPO:0101838', 'abnormal nucleus accumbens morphology', 0.453125, 8.02346099791745, 1.9067330082319718, 'HP:0002060', 'Abnormal cerebral morphology'),
(404298, 'HP:0001355', 'Megalencephaly', 'XPO:0127266', 'abnormally localised anterior hypothalamus', 0.42857142857142855, 6.667568321314008, 1.6904228111816126, 'HP:0100547', 'Abnormal forebrain morphology'),
(404299, 'HP:0001355', 'Megalencephaly', 'XPO:0128750', 'decreased size of the ventricular zone', 0.4067796610169492, 6.005340694266148, 1.562962076284922, 'UPHENO:0081435', 'abnormal anatomical entity morphology in the brain'),
(404300, 'HP:0001355', 'Megalencephaly', 'XPO:0127754', 'abnormally localised suprachiasmatic nucleus', 0.40298507462686567, 6.667568321314008, 1.639185931352649, 'HP:0100547', 'Abnormal forebrain morphology'),
(404301, 'HP:0001355', 'Megalencephaly', 'XPO:0101866', 'abnormal anterior entopeduncular nucleus morphology', 0.453125, 8.02346099791745, 1.9067330082319718, 'HP:0002060', 'Abnormal cerebral morphology'),
(404302, 'HP:0001355', 'Megalencephaly', 'XPO:0101443', 'abnormal subthalamic nucleus', 0.4426229508196721, 6.667568321314008, 1.7179111633526845, 'HP:0100547', 'Abnormal forebrain morphology'),
(404303, 'HP:0001355', 'Megalencephaly', 'XPO:0102419', 'abnormal posterior neural tube morphology', 0.42, 5.483278994082134, 1.5175563177406288, 'HP:0002011', 'Morphological central nervous system abnormality'),
(404304, 'HP:0001355', 'Megalencephaly', 'XPO:0102327', 'abnormal zona limitans intrathalamica morphology', 0.42857142857142855, 6.667568321314008, 1.6904228111816126, 'HP:0100547', 'Abnormal forebrain morphology'),
(404305, 'HP:0001355', 'Megalencephaly', 'XPO:0130649', 'increased size of the accessory olfactory bulb', 0.4027777777777778, 8.02346099791745, 1.7976851200440698, 'HP:0002060', 'Abnormal cerebral morphology'),
(404306, 'HP:0001355', 'Megalencephaly', 'XPO:0101671', 'abnormal olfactory bulb morphology', 0.4393939393939394, 8.02346099791745, 1.8776208710622537, 'HP:0002060', 'Abnormal cerebral morphology'),
(404307, 'HP:0001355', 'Megalencephaly', 'XPO:0140571', 'abnormally necrotic medial pallium', 0.453125, 8.02346099791745, 1.9067330082319718, 'HP:0002060', 'Abnormal cerebral morphology'),
(404308, 'HP:0001355', 'Megalencephaly', 'XPO:0102207', 'abnormal diencephalon morphology', 0.45, 6.667568321314008, 1.7321679319833003, 'HP:0100547', 'Abnormal forebrain morphology'),
(404309, 'HP:0001355', 'Megalencephaly', 'XPO:0130306', 'increased size of the medial amygdala', 0.4084507042253521, 8.02346099791745, 1.810300608993995, 'HP:0002060', 'Abnormal cerebral morphology'),
(404310, 'HP:0001355', 'Megalencephaly', 'XPO:0140228', 'abnormally necrotic telencephalon septum', 0.4264705882352941, 8.02346099791745, 1.8498027277157947, 'HP:0002060', 'Abnormal cerebral morphology'),
(404311, 'HP:0001355', 'Megalencephaly', 'XPO:0100729', 'abnormal thalamus', 0.5, 6.667568321314008, 1.825865318323617, 'HP:0100547', 'Abnormal forebrain morphology'),
(404312, 'HP:0001355', 'Megalencephaly', 'XPO:0101588', 'abnormal central nucleus of the thalamus', 0.47368421052631576, 6.667568321314008, 1.7771668003909757, 'HP:0100547', 'Abnormal forebrain morphology'),
(404313, 'HP:0001355', 'Megalencephaly', 'XPO:0125877', 'absent pretectum', 0.40298507462686567, 6.667568321314008, 1.639185931352649, 'HP:0100547', 'Abnormal forebrain morphology'),
(404314, 'HP:0001355', 'Megalencephaly', 'XPO:0107380', 'abnormal dorsal telencephalon morphology', 0.5, 8.02346099791745, 2.0029304778146257, 'HP:0002060', 'Abnormal cerebral morphology'),
(404315, 'HP:0001355', 'Megalencephaly', 'XPO:0100194', 'abnormal preoptic area', 0.48214285714285715, 6.667568321314008, 1.7929641492884176, 'HP:0100547', 'Abnormal forebrain morphology'),
(404316, 'HP:0001355', 'Megalencephaly', 'XPO:0101664', 'abnormal nervous system morphology', 0.475, 4.7814666189787065, 1.5070489852738316, 'HP:0012639', 'Abnormal nervous system morphology'),
(404317, 'HP:0001355', 'Megalencephaly', 'XPO:0140910', 'abnormally necrotic ventral septum', 0.42028985507246375, 8.02346099791745, 1.8363494384224073, 'HP:0002060', 'Abnormal cerebral morphology'),
(404318, 'HP:0001355', 'Megalencephaly', 'XPO:0130508', 'increased size of the lateral amygdala', 0.4084507042253521, 8.02346099791745, 1.810300608993995, 'HP:0002060', 'Abnormal cerebral morphology'),
(404319, 'HP:0001355', 'Megalencephaly', 'XPO:0129237', 'decreased size of the ventral septum', 0.4084507042253521, 8.02346099791745, 1.810300608993995, 'HP:0002060', 'Abnormal cerebral morphology'),
(404320, 'HP:0001355', 'Megalencephaly', 'XPO:0127341', 'abnormally localised pars intermedia', 0.4153846153846154, 6.667568321314008, 1.6642131181731699, 'HP:0100547', 'Abnormal forebrain morphology'),
(404321, 'HP:0001355', 'Megalencephaly', 'XPO:0129173', 'decreased size of the accessory olfactory bulb', 0.4027777777777778, 8.02346099791745, 1.7976851200440698, 'HP:0002060', 'Abnormal cerebral morphology'),
(404322, 'HP:0001355', 'Megalencephaly', 'XPO:0142058', 'abnormal cerebrospinal fluid morphology', 0.5121951219512195, 5.483278994082134, 1.6758606007262236, 'HP:0002011', 'Morphological central nervous system abnormality'),
(404323, 'HP:0001355', 'Megalencephaly', 'XPO:0141255', 'abnormally necrotic prosomere 5', 0.42028985507246375, 8.02346099791745, 1.8363494384224073, 'HP:0002060', 'Abnormal cerebral morphology'),
(404324, 'HP:0001355', 'Megalencephaly', 'XPO:0101496', 'abnormal subcommissural organ', 0.4909090909090909, 6.667568321314008, 1.8091903999276895, 'HP:0100547', 'Abnormal forebrain morphology'),
(404325, 'HP:0001355', 'Megalencephaly', 'XPO:0129599', 'increased size of the neuromere', 0.4117647058823529, 5.483278994082134, 1.502604659339613, 'HP:0002011', 'Morphological central nervous system abnormality'),
(404326, 'HP:0001355', 'Megalencephaly', 'XPO:0130217', 'increased size of the dorsal telencephalon', 0.4461538461538462, 8.02346099791745, 1.8920089808682852, 'HP:0002060', 'Abnormal cerebral morphology'),
(404327, 'HP:0001355', 'Megalencephaly', 'XPO:0102594', 'abnormal dorsal thalamus morphology', 0.43548387096774194, 6.667568321314008, 1.704000722566664, 'HP:0100547', 'Abnormal forebrain morphology'),
(404328, 'HP:0001355', 'Megalencephaly', 'XPO:0140608', 'abnormally necrotic ventricular zone', 0.42105263157894735, 6.005340694266148, 1.590146063369307, 'UPHENO:0081435', 'abnormal anatomical entity morphology in the brain'),
(404329, 'HP:0001355', 'Megalencephaly', 'XPO:0128766', 'decreased size of the dorsal pallium', 0.4393939393939394, 8.02346099791745, 1.8776208710622537, 'HP:0002060', 'Abnormal cerebral morphology'),
(404330, 'HP:0001355', 'Megalencephaly', 'XPO:0128471', 'decreased size of the anterior amygdala', 0.4084507042253521, 8.02346099791745, 1.810300608993995, 'HP:0002060', 'Abnormal cerebral morphology'),
(404331, 'HP:0001355', 'Megalencephaly', 'XPO:0130244', 'increased size of the dorsal pallium', 0.4393939393939394, 8.02346099791745, 1.8776208710622537, 'HP:0002060', 'Abnormal cerebral morphology'),
(404332, 'HP:0001355', 'Megalencephaly', 'XPO:0125506', 'absent thalamus', 0.40298507462686567, 6.667568321314008, 1.639185931352649, 'HP:0100547', 'Abnormal forebrain morphology'),
(404333, 'HP:0001355', 'Megalencephaly', 'XPO:0101293', 'abnormal posterior hypothalamus', 0.4909090909090909, 6.667568321314008, 1.8091903999276895, 'HP:0100547', 'Abnormal forebrain morphology'),
(404334, 'HP:0001355', 'Megalencephaly', 'XPO:0140029', 'abnormally necrotic basal forebrain', 0.4603174603174603, 8.02346099791745, 1.9218062310018553, 'HP:0002060', 'Abnormal cerebral morphology'),
(404335, 'HP:0001355', 'Megalencephaly', 'XPO:0100698', 'abnormal optic stalk', 0.48214285714285715, 6.667568321314008, 1.7929641492884176, 'HP:0100547', 'Abnormal forebrain morphology'),
(404336, 'HP:0001355', 'Megalencephaly', 'XPO:0101797', 'abnormal lateral pallium morphology', 0.4915254237288136, 8.02346099791745, 1.9858839509832855, 'HP:0002060', 'Abnormal cerebral morphology'),
(404337, 'HP:0001355', 'Megalencephaly', 'XPO:0127125', 'abnormally localised retromammillary area', 0.42857142857142855, 6.667568321314008, 1.6904228111816126, 'HP:0100547', 'Abnormal forebrain morphology'),
(404338, 'HP:0001355', 'Megalencephaly', 'XPO:0102667', 'abnormal ventrolateral neural tube morphology', 0.42, 5.483278994082134, 1.5175563177406288, 'HP:0002011', 'Morphological central nervous system abnormality'),
(404339, 'HP:0001355', 'Megalencephaly', 'XPO:0127014', 'abnormally localised optic stalk', 0.4090909090909091, 6.667568321314008, 1.6515573214369805, 'HP:0100547', 'Abnormal forebrain morphology'),
(404340, 'HP:0001355', 'Megalencephaly', 'XPO:0127924', 'abnormally localised pars nervosa', 0.4090909090909091, 6.667568321314008, 1.6515573214369805, 'HP:0100547', 'Abnormal forebrain morphology'),
(404341, 'HP:0001355', 'Megalencephaly', 'XPO:0127516', 'abnormally localised eminentia thalami', 0.43548387096774194, 6.667568321314008, 1.704000722566664, 'HP:0100547', 'Abnormal forebrain morphology'),
(404342, 'HP:0001355', 'Megalencephaly', 'XPO:0140020', 'abnormally necrotic amygdala', 0.4461538461538462, 8.02346099791745, 1.8920089808682852, 'HP:0002060', 'Abnormal cerebral morphology'),
(404343, 'HP:0001355', 'Megalencephaly', 'XPO:0140421', 'abnormally necrotic anterior entopeduncular region', 0.4915254237288136, 8.02346099791745, 1.9858839509832855, 'HP:0002060', 'Abnormal cerebral morphology'),
(404344, 'HP:0001355', 'Megalencephaly', 'XPO:0130672', 'increased size of the dorsal pallidum', 0.42028985507246375, 8.02346099791745, 1.8363494384224073, 'HP:0002060', 'Abnormal cerebral morphology'),
(404345, 'HP:0001355', 'Megalencephaly', 'XPO:0140125', 'abnormally necrotic presumptive midbrain-hindbrain boundary', 0.42, 5.483278994082134, 1.5175563177406288, 'HP:0002011', 'Morphological central nervous system abnormality'),
(404346, 'HP:0001355', 'Megalencephaly', 'XPO:0102685', 'abnormal anterior hypothalamus morphology', 0.421875, 6.667568321314008, 1.677164388351466, 'HP:0100547', 'Abnormal forebrain morphology'),
(404347, 'HP:0001355', 'Megalencephaly', 'XPO:0100783', 'abnormal supraoptoparaventricular region', 0.46551724137931033, 6.667568321314008, 1.7617797852303152, 'HP:0100547', 'Abnormal forebrain morphology'),
(404348, 'HP:0001355', 'Megalencephaly', 'XPO:0127943', 'abnormally localised anterior thalamic nucleus', 0.4090909090909091, 6.667568321314008, 1.6515573214369805, 'HP:0100547', 'Abnormal forebrain morphology'),
(404349, 'HP:0001355', 'Megalencephaly', 'XPO:0100491', 'abnormal pars distalis', 0.46551724137931033, 6.667568321314008, 1.7617797852303152, 'HP:0100547', 'Abnormal forebrain morphology'),
(404350, 'HP:0001355', 'Megalencephaly', 'XPO:0130942', 'increased size of the anterior entopeduncular nucleus', 0.4027777777777778, 8.02346099791745, 1.7976851200440698, 'HP:0002060', 'Abnormal cerebral morphology'),
(404351, 'HP:0001355', 'Megalencephaly', 'XPO:0103127', 'abnormal torus semicircularis morphology', 0.4067796610169492, 6.005340694266148, 1.562962076284922, 'UPHENO:0081435', 'abnormal anatomical entity morphology in the brain'),
(404352, 'HP:0001355', 'Megalencephaly', 'XPO:0130082', 'increased size of the subpallium', 0.4461538461538462, 8.02346099791745, 1.8920089808682852, 'HP:0002060', 'Abnormal cerebral morphology'),
(404353, 'HP:0001355', 'Megalencephaly', 'XPO:0102986', 'abnormal eminentia thalami morphology', 0.4426229508196721, 6.667568321314008, 1.7179111633526845, 'HP:0100547', 'Abnormal forebrain morphology'),
(404354, 'HP:0001355', 'Megalencephaly', 'XPO:0102765', 'abnormal motor neuron morphology', 0.40425531914893614, 4.7814666189787065, 1.3902997209433732, 'HP:0012639', 'Abnormal nervous system morphology'),
(404355, 'HP:0001355', 'Megalencephaly', 'XPO:0102772', 'abnormal ventrolateral thalamic nucleus morphology', 0.4153846153846154, 6.667568321314008, 1.6642131181731699, 'HP:0100547', 'Abnormal forebrain morphology'),
(404356, 'HP:0001355', 'Megalencephaly', 'XPO:0139879', 'abnormally necrotic telencephalon', 0.46774193548387094, 8.02346099791745, 1.9372426736073256, 'HP:0002060', 'Abnormal cerebral morphology'),
(404357, 'HP:0001355', 'Megalencephaly', 'XPO:0141179', 'abnormally necrotic bed nucleus of the stria terminalis', 0.4084507042253521, 8.02346099791745, 1.810300608993995, 'HP:0002060', 'Abnormal cerebral morphology'),
(404358, 'HP:0001355', 'Megalencephaly', 'XPO:0126519', 'abnormally localised habenula', 0.421875, 6.667568321314008, 1.677164388351466, 'HP:0100547', 'Abnormal forebrain morphology'),
(404359, 'HP:0001355', 'Megalencephaly', 'XPO:0127544', 'abnormally localised neurohypophysis', 0.4153846153846154, 6.667568321314008, 1.6642131181731699, 'HP:0100547', 'Abnormal forebrain morphology'),
(404360, 'HP:0001355', 'Megalencephaly', 'XPO:0126924', 'abnormally localised preoptic area', 0.421875, 6.667568321314008, 1.677164388351466, 'HP:0100547', 'Abnormal forebrain morphology'),
(404361, 'HP:0001355', 'Megalencephaly', 'XPO:0101106', 'abnormal caudal tuberal region', 0.47368421052631576, 6.667568321314008, 1.7771668003909757, 'HP:0100547', 'Abnormal forebrain morphology'),
(404362, 'HP:0001355', 'Megalencephaly', 'XPO:0140226', 'abnormally necrotic subpallium', 0.4603174603174603, 8.02346099791745, 1.9218062310018553, 'HP:0002060', 'Abnormal cerebral morphology'),
(404363, 'HP:0001355', 'Megalencephaly', 'XPO:0102755', 'abnormal third ventricle morphology', 0.43548387096774194, 6.667568321314008, 1.704000722566664, 'HP:0100547', 'Abnormal forebrain morphology'),
(404364, 'HP:0001355', 'Megalencephaly', 'XPO:0102696', 'abnormal accessory olfactory bulb morphology', 0.4461538461538462, 8.02346099791745, 1.8920089808682852, 'HP:0002060', 'Abnormal cerebral morphology'),
(404365, 'HP:0001355', 'Megalencephaly', 'XPO:0125695', 'absent hypothalamus', 0.40298507462686567, 6.667568321314008, 1.639185931352649, 'HP:0100547', 'Abnormal forebrain morphology'),
(404366, 'HP:0001355', 'Megalencephaly', 'XPO:0128119', 'decreased size of the neuromere', 0.4117647058823529, 5.483278994082134, 1.502604659339613, 'HP:0002011', 'Morphological central nervous system abnormality'),
(404367, 'HP:0001355', 'Megalencephaly', 'XPO:0102361', 'abnormal thalamus morphology', 0.4426229508196721, 6.667568321314008, 1.7179111633526845, 'HP:0100547', 'Abnormal forebrain morphology'),
(404368, 'HP:0001355', 'Megalencephaly', 'XPO:0102900', 'abnormal lateral hypothalamic nucleus morphology', 0.40298507462686567, 6.667568321314008, 1.639185931352649, 'HP:0100547', 'Abnormal forebrain morphology'),
(404369, 'HP:0001355', 'Megalencephaly', 'XPO:0141227', 'abnormally necrotic medial amygdala', 0.42028985507246375, 8.02346099791745, 1.8363494384224073, 'HP:0002060', 'Abnormal cerebral morphology'),
(404370, 'HP:0001355', 'Megalencephaly', 'XPO:0101970', 'abnormal lateral ganglionic eminence morphology', 0.48333333333333334, 8.02346099791745, 1.969265383079039, 'HP:0002060', 'Abnormal cerebral morphology'),
(404371, 'HP:0001355', 'Megalencephaly', 'XPO:0126700', 'abnormally localised infundibulum', 0.421875, 6.667568321314008, 1.677164388351466, 'HP:0100547', 'Abnormal forebrain morphology'),
(404372, 'HP:0001355', 'Megalencephaly', 'XPO:0102385', 'abnormal stria terminalis morphology', 0.42105263157894735, 6.005340694266148, 1.590146063369307, 'UPHENO:0081435', 'abnormal anatomical entity morphology in the brain'),
(404373, 'HP:0001355', 'Megalencephaly', 'XPO:0103133', 'abnormal parabrachial area morphology', 0.4666666666666667, 5.483278994082134, 1.5996448138795258, 'HP:0002011', 'Morphological central nervous system abnormality'),
(404374, 'HP:0001355', 'Megalencephaly', 'XPO:0102916', 'abnormal ventromedial thalamic nucleus morphology', 0.4153846153846154, 6.667568321314008, 1.6642131181731699, 'HP:0100547', 'Abnormal forebrain morphology'),
(404375, 'HP:0001355', 'Megalencephaly', 'XPO:0140904', 'abnormally necrotic eminentia thalami', 0.4090909090909091, 6.667568321314008, 1.6515573214369805, 'HP:0100547', 'Abnormal forebrain morphology'),
(404376, 'HP:0001355', 'Megalencephaly', 'XPO:0129897', 'increased size of the diencephalon', 0.40298507462686567, 6.667568321314008, 1.639185931352649, 'HP:0100547', 'Abnormal forebrain morphology'),
(404377, 'HP:0001355', 'Megalencephaly', 'XPO:0101075', 'abnormal mammilary region', 0.48214285714285715, 6.667568321314008, 1.7929641492884176, 'HP:0100547', 'Abnormal forebrain morphology'),
(404378, 'HP:0001355', 'Megalencephaly', 'XPO:0102174', 'abnormal pallium morphology', 0.5, 8.02346099791745, 2.0029304778146257, 'HP:0002060', 'Abnormal cerebral morphology'),
(404379, 'HP:0001355', 'Megalencephaly', 'XPO:0127797', 'abnormally localised ventral hypothalamic nucleus', 0.4090909090909091, 6.667568321314008, 1.6515573214369805, 'HP:0100547', 'Abnormal forebrain morphology'),
(404380, 'HP:0001355', 'Megalencephaly', 'XPO:0101599', 'abnormal raphe nucleus', 0.4067796610169492, 6.005340694266148, 1.562962076284922, 'UPHENO:0081435', 'abnormal anatomical entity morphology in the brain'),
(404381, 'HP:0001355', 'Megalencephaly', 'XPO:0102288', 'abnormal ventral hypothalamic nucleus morphology', 0.40298507462686567, 6.667568321314008, 1.639185931352649, 'HP:0100547', 'Abnormal forebrain morphology'),
(404382, 'HP:0001355', 'Megalencephaly', 'XPO:0140929', 'abnormally necrotic parabrachial area', 0.4117647058823529, 5.483278994082134, 1.502604659339613, 'HP:0002011', 'Morphological central nervous system abnormality'),
(404383, 'HP:0001355', 'Megalencephaly', 'XPO:0129667', 'increased size of the basal ganglion', 0.43283582089552236, 8.02346099791745, 1.8635560972122107, 'HP:0002060', 'Abnormal cerebral morphology'),
(404384, 'HP:0001355', 'Megalencephaly', 'XPO:0127340', 'abnormally localised hypothalamus', 0.43548387096774194, 6.667568321314008, 1.704000722566664, 'HP:0100547', 'Abnormal forebrain morphology'),
(404385, 'HP:0001355', 'Megalencephaly', 'XPO:0102604', 'abnormal ventral pallidum morphology', 0.46774193548387094, 8.02346099791745, 1.9372426736073256, 'HP:0002060', 'Abnormal cerebral morphology'),
(404386, 'HP:0001355', 'Megalencephaly', 'XPO:0130388', 'increased size of the prosomere 5', 0.4084507042253521, 8.02346099791745, 1.810300608993995, 'HP:0002060', 'Abnormal cerebral morphology'),
(404387, 'HP:0001355', 'Megalencephaly', 'XPO:0100914', 'abnormal pars intermedia', 0.46551724137931033, 6.667568321314008, 1.7617797852303152, 'HP:0100547', 'Abnormal forebrain morphology'),
(404388, 'HP:0001355', 'Megalencephaly', 'XPO:0140854', 'abnormally necrotic ventral pallium', 0.453125, 8.02346099791745, 1.9067330082319718, 'HP:0002060', 'Abnormal cerebral morphology'),
(404389, 'HP:0001355', 'Megalencephaly', 'XPO:0139993', 'abnormally necrotic pallidum', 0.4393939393939394, 8.02346099791745, 1.8776208710622537, 'HP:0002060', 'Abnormal cerebral morphology'),
(404390, 'HP:0001355', 'Megalencephaly', 'XPO:0103040', 'abnormal nucleus of the diagonal band morphology', 0.46774193548387094, 8.02346099791745, 1.9372426736073256, 'HP:0002060', 'Abnormal cerebral morphology'),
(404391, 'HP:0001355', 'Megalencephaly', 'XPO:0102247', 'abnormal mitral cell layer of the olfactory bulb morphology', 0.4393939393939394, 8.02346099791745, 1.8776208710622537, 'HP:0002060', 'Abnormal cerebral morphology'),
(404392, 'HP:0001355', 'Megalencephaly', 'XPO:0102131', 'abnormal glomerular layer of the olfactory bulb morphology', 0.4393939393939394, 8.02346099791745, 1.8776208710622537, 'HP:0002060', 'Abnormal cerebral morphology'),
(404393, 'HP:0001355', 'Megalencephaly', 'XPO:0102633', 'abnormal ventricular zone morphology', 0.4444444444444444, 6.005340694266148, 1.6337197766332916, 'UPHENO:0081435', 'abnormal anatomical entity morphology in the brain'),
(404394, 'HP:0001355', 'Megalencephaly', 'XPO:0102219', 'abnormal vestibuloauditory system morphology', 0.4418604651162791, 4.7814666189787065, 1.4535271116150168, 'HP:0012639', 'Abnormal nervous system morphology'),
(404395, 'HP:0001355', 'Megalencephaly', 'XPO:0102066', 'abnormal ventral pallium morphology', 0.4915254237288136, 8.02346099791745, 1.9858839509832855, 'HP:0002060', 'Abnormal cerebral morphology'),
(404396, 'HP:0001355', 'Megalencephaly', 'XPO:0102202', 'abnormal axon morphology', 0.40425531914893614, 4.7814666189787065, 1.3902997209433732, 'HP:0012639', 'Abnormal nervous system morphology'),
(404397, 'HP:0001355', 'Megalencephaly', 'XPO:0140045', 'abnormally necrotic lateral pallium', 0.453125, 8.02346099791745, 1.9067330082319718, 'HP:0002060', 'Abnormal cerebral morphology'),
(404398, 'HP:0001355', 'Megalencephaly', 'XPO:0127309', 'abnormally localised ventromedial thalamic nucleus', 0.4090909090909091, 6.667568321314008, 1.6515573214369805, 'HP:0100547', 'Abnormal forebrain morphology'),
(404399, 'HP:0001355', 'Megalencephaly', 'XPO:0102586', 'abnormal neural progenitor cell morphology', 0.40425531914893614, 4.7814666189787065, 1.3902997209433732, 'HP:0012639', 'Abnormal nervous system morphology'),
(404400, 'HP:0001355', 'Megalencephaly', 'XPO:0129031', 'decreased size of the lateral amygdala', 0.4084507042253521, 8.02346099791745, 1.810300608993995, 'HP:0002060', 'Abnormal cerebral morphology'),
(404401, 'HP:0001355', 'Megalencephaly', 'XPO:0127436', 'abnormally localised prosomere 4', 0.4090909090909091, 6.667568321314008, 1.6515573214369805, 'HP:0100547', 'Abnormal forebrain morphology'),
(404402, 'HP:0001355', 'Megalencephaly', 'XPO:0101564', 'abnormal anterior thalamic nucleus', 0.47368421052631576, 6.667568321314008, 1.7771668003909757, 'HP:0100547', 'Abnormal forebrain morphology'),
(404403, 'HP:0001355', 'Megalencephaly', 'XPO:0127253', 'abnormally localised zona limitans intrathalamica', 0.421875, 6.667568321314008, 1.677164388351466, 'HP:0100547', 'Abnormal forebrain morphology'),
(404404, 'HP:0001355', 'Megalencephaly', 'XPO:0140838', 'abnormally necrotic anterior commissure', 0.453125, 8.02346099791745, 1.9067330082319718, 'HP:0002060', 'Abnormal cerebral morphology'),
(404405, 'HP:0001355', 'Megalencephaly', 'XPO:0129080', 'decreased size of the medial ganglionic eminence', 0.43283582089552236, 8.02346099791745, 1.8635560972122107, 'HP:0002060', 'Abnormal cerebral morphology'),
(404406, 'HP:0001355', 'Megalencephaly', 'XPO:0101420', 'abnormal magnocellular preoptic nucleus', 0.4576271186440678, 6.667568321314008, 1.7467856420423753, 'HP:0100547', 'Abnormal forebrain morphology'),
(404407, 'HP:0001355', 'Megalencephaly', 'XPO:0128950', 'decreased size of the presumptive midbrain-hindbrain boundary', 0.40384615384615385, 5.483278994082134, 1.4880863994491305, 'HP:0002011', 'Morphological central nervous system abnormality'),
(404408, 'HP:0001355', 'Megalencephaly', 'XPO:0101826', 'abnormal preoptic area morphology', 0.4153846153846154, 6.667568321314008, 1.6642131181731699, 'HP:0100547', 'Abnormal forebrain morphology'),
(404409, 'HP:0001355', 'Megalencephaly', 'XPO:0140129', 'abnormally necrotic nucleus of the diagonal band', 0.4264705882352941, 8.02346099791745, 1.8498027277157947, 'HP:0002060', 'Abnormal cerebral morphology'),
(404410, 'HP:0001355', 'Megalencephaly', 'XPO:0126440', 'abnormally localised prethalamus basal plate', 0.4090909090909091, 6.667568321314008, 1.6515573214369805, 'HP:0100547', 'Abnormal forebrain morphology'),
(404411, 'HP:0001355', 'Megalencephaly', 'XPO:0103057', 'abnormal medial amygdala morphology', 0.4603174603174603, 8.02346099791745, 1.9218062310018553, 'HP:0002060', 'Abnormal cerebral morphology'),
(404412, 'HP:0001355', 'Megalencephaly', 'XPO:0126384', 'abnormally localised posterior hypothalamus', 0.42857142857142855, 6.667568321314008, 1.6904228111816126, 'HP:0100547', 'Abnormal forebrain morphology'),
(404413, 'HP:0001355', 'Megalencephaly', 'XPO:0128910', 'decreased size of the prosomere 5', 0.4084507042253521, 8.02346099791745, 1.810300608993995, 'HP:0002060', 'Abnormal cerebral morphology'),
(404414, 'HP:0001355', 'Megalencephaly', 'XPO:0101140', 'abnormal ventrolateral thalamic nucleus', 0.47368421052631576, 6.667568321314008, 1.7771668003909757, 'HP:0100547', 'Abnormal forebrain morphology'),
(404415, 'HP:0001355', 'Megalencephaly', 'XPO:0127076', 'abnormally localised dorsal thalamus', 0.42857142857142855, 6.667568321314008, 1.6904228111816126, 'HP:0100547', 'Abnormal forebrain morphology'),
(404416, 'HP:0001355', 'Megalencephaly', 'XPO:0130713', 'increased size of the ventral septum', 0.4084507042253521, 8.02346099791745, 1.810300608993995, 'HP:0002060', 'Abnormal cerebral morphology'),
(404417, 'HP:0001355', 'Megalencephaly', 'XPO:0102392', 'abnormal Stirnorgan morphology', 0.4222222222222222, 4.7814666189787065, 1.4208594094232423, 'HP:0012639', 'Abnormal nervous system morphology'),
(404418, 'HP:0001355', 'Megalencephaly', 'XPO:0103728', 'increased size of the forebrain', 0.4153846153846154, 6.667568321314008, 1.6642131181731699, 'HP:0100547', 'Abnormal forebrain morphology'),
(404419, 'HP:0001355', 'Megalencephaly', 'XPO:0129494', 'increased size of the neural nucleus', 0.42, 5.483278994082134, 1.5175563177406288, 'HP:0002011', 'Morphological central nervous system abnormality'),
(404420, 'HP:0001355', 'Megalencephaly', 'XPO:0128704', 'decreased size of the lateral pallium', 0.4393939393939394, 8.02346099791745, 1.8776208710622537, 'HP:0002060', 'Abnormal cerebral morphology'),
(404421, 'HP:0001355', 'Megalencephaly', 'XPO:0127530', 'abnormally localised third ventricle', 0.42857142857142855, 6.667568321314008, 1.6904228111816126, 'HP:0100547', 'Abnormal forebrain morphology'),
(404422, 'HP:0001355', 'Megalencephaly', 'XPO:0128276', 'decreased size of the amygdala', 0.43283582089552236, 8.02346099791745, 1.8635560972122107, 'HP:0002060', 'Abnormal cerebral morphology'),
(404423, 'HP:0001355', 'Megalencephaly', 'XPO:0130085', 'increased size of the telencephalon septum', 0.4142857142857143, 8.02346099791745, 1.8231854734408677, 'HP:0002060', 'Abnormal cerebral morphology'),
(404424, 'HP:0001355', 'Megalencephaly', 'XPO:0129429', 'decreased size of the anterior commissure', 0.4393939393939394, 8.02346099791745, 1.8776208710622537, 'HP:0002060', 'Abnormal cerebral morphology'),
(404425, 'HP:0001355', 'Megalencephaly', 'XPO:0100473', 'abnormal ventral habenular nucleus', 0.4576271186440678, 6.667568321314008, 1.7467856420423753, 'HP:0100547', 'Abnormal forebrain morphology'),
(404426, 'HP:0001355', 'Megalencephaly', 'XPO:0140213', 'abnormally necrotic diencephalon', 0.4153846153846154, 6.667568321314008, 1.6642131181731699, 'HP:0100547', 'Abnormal forebrain morphology'),
(404427, 'HP:0001355', 'Megalencephaly', 'XPO:0130165', 'increased size of the central nervous system', 0.42, 5.483278994082134, 1.5175563177406288, 'HP:0002011', 'Morphological central nervous system abnormality'),
(404428, 'HP:0001355', 'Megalencephaly', 'XPO:0102854', 'abnormal medial septum morphology', 0.4603174603174603, 8.02346099791745, 1.9218062310018553, 'HP:0002060', 'Abnormal cerebral morphology'),
(404429, 'HP:0001355', 'Megalencephaly', 'XPO:0100695', 'abnormal zona limitans intrathalamica', 0.4909090909090909, 6.667568321314008, 1.8091903999276895, 'HP:0100547', 'Abnormal forebrain morphology'),
(404430, 'HP:0001355', 'Megalencephaly', 'XPO:0102191', 'abnormal telencephalon morphology', 0.5087719298245614, 8.02346099791745, 2.020423652549772, 'HP:0002060', 'Abnormal cerebral morphology'),
(404431, 'HP:0001355', 'Megalencephaly', 'XPO:0128398', 'decreased size of the nucleus of the diagonal band', 0.4142857142857143, 8.02346099791745, 1.8231854734408677, 'HP:0002060', 'Abnormal cerebral morphology'),
(404432, 'HP:0001355', 'Megalencephaly', 'XPO:0101828', 'abnormal neuron morphology', 0.4222222222222222, 4.7814666189787065, 1.4208594094232423, 'HP:0012639', 'Abnormal nervous system morphology'),
(404433, 'HP:0001355', 'Megalencephaly', 'XPO:0126843', 'abnormally localised pars distalis', 0.4090909090909091, 6.667568321314008, 1.6515573214369805, 'HP:0100547', 'Abnormal forebrain morphology'),
(404434, 'HP:0001355', 'Megalencephaly', 'XPO:0107340', 'abnormal enteric nervous system morphology', 0.4523809523809524, 4.7814666189787065, 1.4707292146657451, 'HP:0012639', 'Abnormal nervous system morphology'),
(404435, 'HP:0001355', 'Megalencephaly', 'XPO:0128739', 'decreased size of the dorsal telencephalon', 0.4461538461538462, 8.02346099791745, 1.8920089808682852, 'HP:0002060', 'Abnormal cerebral morphology'),
(404436, 'HP:0001355', 'Megalencephaly', 'XPO:0142044', 'increased size of the cerebrospinal fluid', 0.45652173913043476, 5.483278994082134, 1.5821618319614958, 'HP:0002011', 'Morphological central nervous system abnormality'),
(404437, 'HP:0001355', 'Megalencephaly', 'XPO:0102282', 'abnormal prosomere morphology', 0.423728813559322, 6.65028457999709, 1.6786653016352073, 'UPHENO:0087518', 'abnormal forebrain morphology'),
(404438, 'HP:0001355', 'Megalencephaly', 'XPO:0129399', 'decreased size of the medial pallium', 0.4393939393939394, 8.02346099791745, 1.8776208710622537, 'HP:0002060', 'Abnormal cerebral morphology'),
(404439, 'HP:0001355', 'Megalencephaly', 'XPO:0101746', 'abnormal peripheral nervous system morphology', 0.41304347826086957, 4.7814666189787065, 1.405330425021534, 'HP:0012639', 'Abnormal nervous system morphology'),
(404440, 'HP:0001355', 'Megalencephaly', 'XPO:0129878', 'increased size of the nucleus of the diagonal band', 0.4142857142857143, 8.02346099791745, 1.8231854734408677, 'HP:0002060', 'Abnormal cerebral morphology'),
(404441, 'HP:0001355', 'Megalencephaly', 'XPO:0102330', 'abnormal optic stalk morphology', 0.4153846153846154, 6.667568321314008, 1.6642131181731699, 'HP:0100547', 'Abnormal forebrain morphology'),
(404442, 'HP:0001355', 'Megalencephaly', 'XPO:0129298', 'decreased size of the nucleus accumbens', 0.4027777777777778, 8.02346099791745, 1.7976851200440698, 'HP:0002060', 'Abnormal cerebral morphology'),
(404443, 'HP:0001355', 'Megalencephaly', 'XPO:0102630', 'abnormal rostral tuberal region morphology', 0.4090909090909091, 6.667568321314008, 1.6515573214369805, 'HP:0100547', 'Abnormal forebrain morphology'),
(404444, 'HP:0001355', 'Megalencephaly', 'XPO:0103128', 'abnormal subcommissural organ morphology', 0.42857142857142855, 6.667568321314008, 1.6904228111816126, 'HP:0100547', 'Abnormal forebrain morphology'),
(404445, 'HP:0001355', 'Megalencephaly', 'XPO:0141233', 'abnormally necrotic lateral amygdala', 0.42028985507246375, 8.02346099791745, 1.8363494384224073, 'HP:0002060', 'Abnormal cerebral morphology'),
(404446, 'HP:0001355', 'Megalencephaly', 'XPO:0103341', 'decreased size of the forebrain', 0.4153846153846154, 6.667568321314008, 1.6642131181731699, 'HP:0100547', 'Abnormal forebrain morphology'),
(404447, 'HP:0001355', 'Megalencephaly', 'XPO:0102200', 'abnormal telencephalon septum morphology', 0.46774193548387094, 8.02346099791745, 1.9372426736073256, 'HP:0002060', 'Abnormal cerebral morphology'),
(404448, 'HP:0001355', 'Megalencephaly', 'XPO:0130920', 'increased size of the dorsal septum', 0.4084507042253521, 8.02346099791745, 1.810300608993995, 'HP:0002060', 'Abnormal cerebral morphology'),
(404449, 'HP:0001355', 'Megalencephaly', 'XPO:0102749', 'abnormal tuberal region morphology', 0.4153846153846154, 6.667568321314008, 1.6642131181731699, 'HP:0100547', 'Abnormal forebrain morphology'),
(404450, 'HP:0001355', 'Megalencephaly', 'XPO:0125862', 'absent eminentia thalami', 0.40298507462686567, 6.667568321314008, 1.639185931352649, 'HP:0100547', 'Abnormal forebrain morphology'),
(404451, 'HP:0001355', 'Megalencephaly', 'XPO:0102548', 'abnormal principal cavity morphology', 0.4418604651162791, 4.7814666189787065, 1.4535271116150168, 'HP:0012639', 'Abnormal nervous system morphology'),
(404452, 'HP:0001355', 'Megalencephaly', 'XPO:0101526', 'abnormal infundibulum', 0.48214285714285715, 6.667568321314008, 1.7929641492884176, 'HP:0100547', 'Abnormal forebrain morphology'),
(404453, 'HP:0001355', 'Megalencephaly', 'XPO:0101186', 'abnormal optic chiasm', 0.5, 6.667568321314008, 1.825865318323617, 'HP:0100547', 'Abnormal forebrain morphology'),
(404454, 'HP:0001355', 'Megalencephaly', 'XPO:0130428', 'increased size of the presumptive midbrain-hindbrain boundary', 0.40384615384615385, 5.483278994082134, 1.4880863994491305, 'HP:0002011', 'Morphological central nervous system abnormality'),
(404455, 'HP:0001355', 'Megalencephaly', 'XPO:0101905', 'abnormal visual system morphology', 0.4418604651162791, 4.7814666189787065, 1.4535271116150168, 'HP:0012639', 'Abnormal nervous system morphology'),
(404456, 'HP:0001355', 'Megalencephaly', 'XPO:0127670', 'abnormally localised lateral hypothalamic nucleus', 0.4090909090909091, 6.667568321314008, 1.6515573214369805, 'HP:0100547', 'Abnormal forebrain morphology'),
(404457, 'HP:0001355', 'Megalencephaly', 'XPO:0101351', 'abnormal dorsal habenular nucleus', 0.4576271186440678, 6.667568321314008, 1.7467856420423753, 'HP:0100547', 'Abnormal forebrain morphology'),
(404458, 'HP:0001355', 'Megalencephaly', 'XPO:0100988', 'abnormal habenula', 0.48214285714285715, 6.667568321314008, 1.7929641492884176, 'HP:0100547', 'Abnormal forebrain morphology'),
(404459, 'HP:0001355', 'Megalencephaly', 'XPO:0140330', 'abnormally necrotic dorsal pallidum', 0.43283582089552236, 8.02346099791745, 1.8635560972122107, 'HP:0002060', 'Abnormal cerebral morphology'),
(404460, 'HP:0001355', 'Megalencephaly', 'XPO:0100998', 'abnormal rostral tuberal region', 0.47368421052631576, 6.667568321314008, 1.7771668003909757, 'HP:0100547', 'Abnormal forebrain morphology'),
(404461, 'HP:0001355', 'Megalencephaly', 'XPO:0129939', 'increased size of the prosomere 6', 0.4084507042253521, 8.02346099791745, 1.810300608993995, 'HP:0002060', 'Abnormal cerebral morphology'),
(404462, 'HP:0001355', 'Megalencephaly', 'XPO:0141044', 'abnormally necrotic anterior amygdala', 0.42028985507246375, 8.02346099791745, 1.8363494384224073, 'HP:0002060', 'Abnormal cerebral morphology'),
(404463, 'HP:0001355', 'Megalencephaly', 'XPO:0102738', 'abnormal caudal tuberal region morphology', 0.4090909090909091, 6.667568321314008, 1.6515573214369805, 'HP:0100547', 'Abnormal forebrain morphology'),
(404464, 'HP:0001355', 'Megalencephaly', 'XPO:0102249', 'abnormal forebrain morphology', 0.48214285714285715, 6.667568321314008, 1.7929641492884176, 'HP:0100547', 'Abnormal forebrain morphology'),
(404465, 'HP:0001355', 'Megalencephaly', 'XPO:0140412', 'abnormally necrotic lateral septum', 0.42028985507246375, 8.02346099791745, 1.8363494384224073, 'HP:0002060', 'Abnormal cerebral morphology'),
(404466, 'HP:0001355', 'Megalencephaly', 'XPO:0101796', 'abnormal neural nucleus morphology', 0.4883720930232558, 5.483278994082134, 1.6364230623437035, 'HP:0002011', 'Morphological central nervous system abnormality'),
(404467, 'HP:0001355', 'Megalencephaly', 'XPO:0102235', 'abnormal lateral ventricle morphology', 0.42105263157894735, 6.005340694266148, 1.590146063369307, 'UPHENO:0081435', 'abnormal anatomical entity morphology in the brain'),
(404468, 'HP:0001355', 'Megalencephaly', 'XPO:0142031', 'abnormally necrotic cerebrospinal fluid', 0.4772727272727273, 5.483278994082134, 1.617720470261422, 'HP:0002011', 'Morphological central nervous system abnormality'),
(404469, 'HP:0001355', 'Megalencephaly', 'XPO:0101807', 'abnormal migrating neuroblast morphology', 0.4222222222222222, 4.7814666189787065, 1.4208594094232423, 'HP:0012639', 'Abnormal nervous system morphology'),
(404470, 'HP:0001355', 'Megalencephaly', 'XPO:0129372', 'decreased size of the anterior entopeduncular region', 0.47540983606557374, 8.02346099791745, 1.9530571619126922, 'HP:0002060', 'Abnormal cerebral morphology'),
(404471, 'HP:0001355', 'Megalencephaly', 'XPO:0129720', 'increased size of the pallidum', 0.4264705882352941, 8.02346099791745, 1.8498027277157947, 'HP:0002060', 'Abnormal cerebral morphology'),
(404472, 'HP:0001355', 'Megalencephaly', 'XPO:0100909', 'abnormal choroid fissure', 0.45, 6.667568321314008, 1.7321679319833003, 'HP:0100547', 'Abnormal forebrain morphology'),
(404473, 'HP:0001355', 'Megalencephaly', 'XPO:0131750', 'abnormal opening of the anterior neural tube', 0.40384615384615385, 5.483278994082134, 1.4880863994491305, 'HP:0002011', 'Morphological central nervous system abnormality'),
(404474, 'HP:0001355', 'Megalencephaly', 'XPO:0128240', 'decreased size of the pallidum', 0.4264705882352941, 8.02346099791745, 1.8498027277157947, 'HP:0002060', 'Abnormal cerebral morphology'),
(404475, 'HP:0001355', 'Megalencephaly', 'XPO:0127245', 'abnormally localised caudal tuberal region', 0.4153846153846154, 6.667568321314008, 1.6642131181731699, 'HP:0100547', 'Abnormal forebrain morphology'),
(404476, 'HP:0001355', 'Megalencephaly', 'XPO:0128686', 'decreased size of the central nervous system', 0.42, 5.483278994082134, 1.5175563177406288, 'HP:0002011', 'Morphological central nervous system abnormality'),
(404477, 'HP:0001355', 'Megalencephaly', 'XPO:0101793', 'abnormal hindbrain morphology', 0.4067796610169492, 6.005340694266148, 1.562962076284922, 'UPHENO:0081435', 'abnormal anatomical entity morphology in the brain'),
(404478, 'HP:0001355', 'Megalencephaly', 'XPO:0130774', 'increased size of the nucleus accumbens', 0.4027777777777778, 8.02346099791745, 1.7976851200440698, 'HP:0002060', 'Abnormal cerebral morphology'),
(404479, 'HP:0001355', 'Megalencephaly', 'XPO:0103146', 'abnormal dendrite morphology', 0.40425531914893614, 4.7814666189787065, 1.3902997209433732, 'HP:0012639', 'Abnormal nervous system morphology'),
(404480, 'HP:0001355', 'Megalencephaly', 'XPO:0102792', 'abnormal ventral funiculus morphology', 0.42, 5.483278994082134, 1.5175563177406288, 'HP:0002011', 'Morphological central nervous system abnormality'),
(404481, 'HP:0001355', 'Megalencephaly', 'XPO:0102972', 'abnormal lateral forebrain bundle morphology', 0.43103448275862066, 6.65028457999709, 1.6930747101462111, 'UPHENO:0087518', 'abnormal forebrain morphology'),
(404482, 'HP:0001355', 'Megalencephaly', 'XPO:0103470', 'abnormal closing of the posterior neural tube', 0.40384615384615385, 5.483278994082134, 1.4880863994491305, 'HP:0002011', 'Morphological central nervous system abnormality'),
(404483, 'HP:0001355', 'Megalencephaly', 'XPO:0127938', 'abnormally localised mammilary region', 0.421875, 6.667568321314008, 1.677164388351466, 'HP:0100547', 'Abnormal forebrain morphology'),
(404484, 'HP:0001355', 'Megalencephaly', 'XPO:0102333', 'abnormal microglial cell morphology', 0.40425531914893614, 4.7814666189787065, 1.3902997209433732, 'HP:0012639', 'Abnormal nervous system morphology'),
(404485, 'HP:0001355', 'Megalencephaly', 'XPO:0102238', 'abnormal basal forebrain morphology', 0.5, 8.02346099791745, 2.0029304778146257, 'HP:0002060', 'Abnormal cerebral morphology'),
(404486, 'HP:0001355', 'Megalencephaly', 'XPO:0127044', 'abnormally localised central nucleus of the thalamus', 0.4090909090909091, 6.667568321314008, 1.6515573214369805, 'HP:0100547', 'Abnormal forebrain morphology'),
(404487, 'HP:0001355', 'Megalencephaly', 'XPO:0140066', 'abnormally necrotic prosomere 6', 0.42028985507246375, 8.02346099791745, 1.8363494384224073, 'HP:0002060', 'Abnormal cerebral morphology'),
(404488, 'HP:0001355', 'Megalencephaly', 'XPO:0140424', 'abnormally necrotic dorsal septum', 0.42028985507246375, 8.02346099791745, 1.8363494384224073, 'HP:0002060', 'Abnormal cerebral morphology'),
(404489, 'HP:0001355', 'Megalencephaly', 'XPO:0126708', 'abnormally localised supraoptoparaventricular region', 0.40298507462686567, 6.667568321314008, 1.639185931352649, 'HP:0100547', 'Abnormal forebrain morphology'),
(404490, 'HP:0001355', 'Megalencephaly', 'XPO:0103058', 'abnormal dorsal funiculus morphology', 0.42, 5.483278994082134, 1.5175563177406288, 'HP:0002011', 'Morphological central nervous system abnormality'),
(404491, 'HP:0001355', 'Megalencephaly', 'XPO:0128417', 'decreased size of the diencephalon', 0.40298507462686567, 6.667568321314008, 1.639185931352649, 'HP:0100547', 'Abnormal forebrain morphology'),
(404492, 'HP:0001355', 'Megalencephaly', 'XPO:0140628', 'abnormally necrotic glomerular layer of the olfactory bulb', 0.4084507042253521, 8.02346099791745, 1.810300608993995, 'HP:0002060', 'Abnormal cerebral morphology'),
(404493, 'HP:0001355', 'Megalencephaly', 'XPO:0100315', 'abnormal neurohypophysis', 0.47368421052631576, 6.667568321314008, 1.7771668003909757, 'HP:0100547', 'Abnormal forebrain morphology'),
(404494, 'HP:0001355', 'Megalencephaly', 'XPO:0140065', 'abnormally necrotic ventral pallidum', 0.43283582089552236, 8.02346099791745, 1.8635560972122107, 'HP:0002060', 'Abnormal cerebral morphology'),
(404495, 'HP:0001355', 'Megalencephaly', 'XPO:0102978', 'abnormal prosomere 6 morphology', 0.46774193548387094, 8.02346099791745, 1.9372426736073256, 'HP:0002060', 'Abnormal cerebral morphology'),
(404496, 'HP:0001355', 'Megalencephaly', 'XPO:0140544', 'abnormally necrotic forebrain', 0.4426229508196721, 6.667568321314008, 1.7179111633526845, 'HP:0100547', 'Abnormal forebrain morphology'),
(404497, 'HP:0001355', 'Megalencephaly', 'XPO:0130187', 'increased size of the basal forebrain', 0.4461538461538462, 8.02346099791745, 1.8920089808682852, 'HP:0002060', 'Abnormal cerebral morphology'),
(404498, 'HP:0001355', 'Megalencephaly', 'XPO:0101906', 'abnormal sensory system morphology', 0.4634146341463415, 4.7814666189787065, 1.488556886355695, 'HP:0012639', 'Abnormal nervous system morphology'),
(404499, 'HP:0001355', 'Megalencephaly', 'XPO:0101972', 'abnormal midbrain morphology', 0.41379310344827586, 6.005340694266148, 1.5763783058468588, 'UPHENO:0081435', 'abnormal anatomical entity morphology in the brain'),
(404500, 'HP:0001355', 'Megalencephaly', 'XPO:0100763', 'abnormal pretectum', 0.5, 6.667568321314008, 1.825865318323617, 'HP:0100547', 'Abnormal forebrain morphology'),
(404501, 'HP:0001355', 'Megalencephaly', 'XPO:0140076', 'abnormally necrotic granule cell layer of the olfactory bulb', 0.4084507042253521, 8.02346099791745, 1.810300608993995, 'HP:0002060', 'Abnormal cerebral morphology'),
(404502, 'HP:0001355', 'Megalencephaly', 'XPO:0101790', 'abnormal neuromere morphology', 0.4772727272727273, 5.483278994082134, 1.617720470261422, 'HP:0002011', 'Morphological central nervous system abnormality'),
(404503, 'HP:0001355', 'Megalencephaly', 'XPO:0127157', 'abnormally localised ventrolateral thalamic nucleus', 0.4090909090909091, 6.667568321314008, 1.6515573214369805, 'HP:0100547', 'Abnormal forebrain morphology'),
(404504, 'HP:0001355', 'Megalencephaly', 'XPO:0129756', 'increased size of the amygdala', 0.43283582089552236, 8.02346099791745, 1.8635560972122107, 'HP:0002060', 'Abnormal cerebral morphology'),
(404505, 'HP:0001355', 'Megalencephaly', 'XPO:0128605', 'decreased size of the telencephalon septum', 0.4142857142857143, 8.02346099791745, 1.8231854734408677, 'HP:0002060', 'Abnormal cerebral morphology'),
(404506, 'HP:0001355', 'Megalencephaly', 'XPO:0103196', 'abnormal anterior thalamic nucleus morphology', 0.4153846153846154, 6.667568321314008, 1.6642131181731699, 'HP:0100547', 'Abnormal forebrain morphology'),
(404507, 'HP:0001355', 'Megalencephaly', 'XPO:0102819', 'abnormal dorsolateral commissural neuron morphology', 0.40425531914893614, 4.7814666189787065, 1.3902997209433732, 'HP:0012639', 'Abnormal nervous system morphology'),
(404508, 'HP:0001355', 'Megalencephaly', 'XPO:0102925', 'abnormal posterior hypothalamus morphology', 0.421875, 6.667568321314008, 1.677164388351466, 'HP:0100547', 'Abnormal forebrain morphology'),
(404509, 'HP:0001355', 'Megalencephaly', 'XPO:0100263', 'abnormal prethalamus', 0.4909090909090909, 6.667568321314008, 1.8091903999276895, 'HP:0100547', 'Abnormal forebrain morphology'),
(404510, 'HP:0001355', 'Megalencephaly', 'XPO:0100195', 'abnormal retromammillary area', 0.4909090909090909, 6.667568321314008, 1.8091903999276895, 'HP:0100547', 'Abnormal forebrain morphology'),
(404511, 'HP:0001355', 'Megalencephaly', 'XPO:0142037', 'decreased size of the cerebrospinal fluid', 0.45652173913043476, 5.483278994082134, 1.5821618319614958, 'HP:0002011', 'Morphological central nervous system abnormality'),
(404512, 'HP:0001355', 'Megalencephaly', 'XPO:0102070', 'abnormal spinal cord morphology', 0.42, 5.483278994082134, 1.5175563177406288, 'HP:0002011', 'Morphological central nervous system abnormality'),
(404513, 'HP:0001355', 'Megalencephaly', 'XPO:0129909', 'increased size of the pallium', 0.4461538461538462, 8.02346099791745, 1.8920089808682852, 'HP:0002060', 'Abnormal cerebral morphology'),
(404514, 'HP:0001355', 'Megalencephaly', 'XPO:0127531', 'abnormally localised pretectum', 0.43548387096774194, 6.667568321314008, 1.704000722566664, 'HP:0100547', 'Abnormal forebrain morphology'),
(404515, 'HP:0001355', 'Megalencephaly', 'XPO:0101123', 'abnormal third ventricle', 0.48214285714285715, 6.667568321314008, 1.7929641492884176, 'HP:0100547', 'Abnormal forebrain morphology'),
(404516, 'HP:0001355', 'Megalencephaly', 'XPO:0130846', 'increased size of the anterior entopeduncular region', 0.47540983606557374, 8.02346099791745, 1.9530571619126922, 'HP:0002060', 'Abnormal cerebral morphology'),
(404517, 'HP:0001355', 'Megalencephaly', 'XPO:0129462', 'decreased size of the medial septum', 0.4084507042253521, 8.02346099791745, 1.810300608993995, 'HP:0002060', 'Abnormal cerebral morphology'),
(404518, 'HP:0001355', 'Megalencephaly', 'XPO:0130903', 'increased size of the anterior commissure', 0.4393939393939394, 8.02346099791745, 1.8776208710622537, 'HP:0002060', 'Abnormal cerebral morphology'),
(404519, 'HP:0001355', 'Megalencephaly', 'XPO:0130603', 'increased size of the lateral ganglionic eminence', 0.43283582089552236, 8.02346099791745, 1.8635560972122107, 'HP:0002060', 'Abnormal cerebral morphology'),
(404520, 'HP:0001355', 'Megalencephaly', 'XPO:0115310', 'abnormally incomplete structure of forebrain', 0.47368421052631576, 6.667568321314008, 1.7771668003909757, 'HP:0100547', 'Abnormal forebrain morphology'),
(404521, 'HP:0001355', 'Megalencephaly', 'XPO:0127901', 'abnormally localised rostral tuberal region', 0.4153846153846154, 6.667568321314008, 1.6642131181731699, 'HP:0100547', 'Abnormal forebrain morphology'),
(404522, 'HP:0001355', 'Megalencephaly', 'XPO:0141224', 'abnormally necrotic dorsal telencephalon', 0.4603174603174603, 8.02346099791745, 1.9218062310018553, 'HP:0002060', 'Abnormal cerebral morphology'),
(404523, 'HP:0001355', 'Megalencephaly', 'XPO:0102357', 'abnormal subpallium morphology', 0.5, 8.02346099791745, 2.0029304778146257, 'HP:0002060', 'Abnormal cerebral morphology'),
(404524, 'HP:0001355', 'Megalencephaly', 'XPO:0129446', 'decreased size of the dorsal septum', 0.4084507042253521, 8.02346099791745, 1.810300608993995, 'HP:0002060', 'Abnormal cerebral morphology'),
(404525, 'HP:0001355', 'Megalencephaly', 'XPO:0140468', 'abnormally necrotic central nervous system', 0.4375, 5.483278994082134, 1.5488494310006167, 'HP:0002011', 'Morphological central nervous system abnormality'),
(404526, 'HP:0001355', 'Megalencephaly', 'XPO:0125252', 'absent diencephalon', 0.40298507462686567, 6.667568321314008, 1.639185931352649, 'HP:0100547', 'Abnormal forebrain morphology'),
(404527, 'HP:0001355', 'Megalencephaly', 'XPO:0101268', 'abnormal lateral hypothalamic nucleus', 0.47368421052631576, 6.667568321314008, 1.7771668003909757, 'HP:0100547', 'Abnormal forebrain morphology'),
(404528, 'HP:0001355', 'Megalencephaly', 'XPO:0128428', 'decreased size of the ventral pallidum', 0.42028985507246375, 8.02346099791745, 1.8363494384224073, 'HP:0002060', 'Abnormal cerebral morphology'),
(404529, 'HP:0001355', 'Megalencephaly', 'XPO:0127091', 'abnormally localised choroid fissure', 0.40298507462686567, 6.667568321314008, 1.639185931352649, 'HP:0100547', 'Abnormal forebrain morphology'),
(404530, 'HP:0001355', 'Megalencephaly', 'XPO:0128818', 'decreased size of the lateral septum', 0.4084507042253521, 8.02346099791745, 1.810300608993995, 'HP:0002060', 'Abnormal cerebral morphology'),
(404531, 'HP:0001355', 'Megalencephaly', 'XPO:0140575', 'abnormally necrotic medial septum', 0.42028985507246375, 8.02346099791745, 1.8363494384224073, 'HP:0002060', 'Abnormal cerebral morphology'),
(404532, 'HP:0001355', 'Megalencephaly', 'XPO:0127365', 'abnormally localised melanotrope', 0.40298507462686567, 6.667568321314008, 1.639185931352649, 'HP:0100547', 'Abnormal forebrain morphology'),
(404533, 'HP:0001355', 'Megalencephaly', 'XPO:0102389', 'abnormal bed nucleus of the stria terminalis morphology', 0.4461538461538462, 8.02346099791745, 1.8920089808682852, 'HP:0002060', 'Abnormal cerebral morphology'),
(404534, 'HP:0001355', 'Megalencephaly', 'XPO:0127949', 'abnormally localised optic tract', 0.43548387096774194, 6.667568321314008, 1.704000722566664, 'HP:0100547', 'Abnormal forebrain morphology'),
(404535, 'HP:0001355', 'Megalencephaly', 'XPO:0103200', 'abnormal prosomere 5 morphology', 0.46774193548387094, 8.02346099791745, 1.9372426736073256, 'HP:0002060', 'Abnormal cerebral morphology'),
(404536, 'HP:0001355', 'Megalencephaly', 'XPO:0129924', 'increased size of the telencephalon', 0.453125, 8.02346099791745, 1.9067330082319718, 'HP:0002060', 'Abnormal cerebral morphology'),
(404537, 'HP:0001355', 'Megalencephaly', 'XPO:0100233', 'abnormal pars nervosa', 0.46551724137931033, 6.667568321314008, 1.7617797852303152, 'HP:0100547', 'Abnormal forebrain morphology'),
(404538, 'HP:0001355', 'Megalencephaly', 'XPO:0140818', 'abnormally necrotic pretectum', 0.40298507462686567, 6.667568321314008, 1.639185931352649, 'HP:0100547', 'Abnormal forebrain morphology'),
(404539, 'HP:0001355', 'Megalencephaly', 'XPO:0140221', 'abnormally necrotic nervous system', 0.4222222222222222, 4.7814666189787065, 1.4208594094232423, 'HP:0012639', 'Abnormal nervous system morphology'),
(404540, 'HP:0001355', 'Megalencephaly', 'XPO:0141028', 'abnormally necrotic external plexiform layer of the olfactory bulb', 0.4084507042253521, 8.02346099791745, 1.810300608993995, 'HP:0002060', 'Abnormal cerebral morphology'),
(404541, 'HP:0001355', 'Megalencephaly', 'XPO:0102496', 'abnormal dorsolateral ascending neuron morphology', 0.40425531914893614, 4.7814666189787065, 1.3902997209433732, 'HP:0012639', 'Abnormal nervous system morphology'),
(404542, 'HP:0001355', 'Megalencephaly', 'XPO:0102707', 'abnormal mammilary region morphology', 0.4153846153846154, 6.667568321314008, 1.6642131181731699, 'HP:0100547', 'Abnormal forebrain morphology'),
(404543, 'HP:0001355', 'Megalencephaly', 'XPO:0129127', 'decreased size of the lateral ganglionic eminence', 0.43283582089552236, 8.02346099791745, 1.8635560972122107, 'HP:0002060', 'Abnormal cerebral morphology'),
(404544, 'HP:0001355', 'Megalencephaly', 'XPO:0102826', 'abnormal anterior commissure morphology', 0.4915254237288136, 8.02346099791745, 1.9858839509832855, 'HP:0002060', 'Abnormal cerebral morphology'),
(404545, 'HP:0001355', 'Megalencephaly', 'XPO:0128429', 'decreased size of the pallium', 0.4461538461538462, 8.02346099791745, 1.8920089808682852, 'HP:0002060', 'Abnormal cerebral morphology'),
(404546, 'HP:0001355', 'Megalencephaly', 'XPO:0128828', 'decreased size of the medial amygdala', 0.4084507042253521, 8.02346099791745, 1.810300608993995, 'HP:0002060', 'Abnormal cerebral morphology'),
(404547, 'HP:0001355', 'Megalencephaly', 'XPO:0128014', 'decreased size of the neural nucleus', 0.42, 5.483278994082134, 1.5175563177406288, 'HP:0002011', 'Morphological central nervous system abnormality'),
(404548, 'HP:0001355', 'Megalencephaly', 'XPO:0101986', 'abnormal amygdala morphology', 0.48333333333333334, 8.02346099791745, 1.969265383079039, 'HP:0002060', 'Abnormal cerebral morphology'),
(404549, 'HP:0001355', 'Megalencephaly', 'XPO:0115482', 'abnormally pigmented optic stalk', 0.4090909090909091, 6.667568321314008, 1.6515573214369805, 'HP:0100547', 'Abnormal forebrain morphology'),
(404550, 'HP:0001355', 'Megalencephaly', 'XPO:0141286', 'abnormal neuron projection morphology', 0.4222222222222222, 4.7814666189787065, 1.4208594094232423, 'HP:0012639', 'Abnormal nervous system morphology'),
(404551, 'HP:0001355', 'Megalencephaly', 'XPO:0101068', 'abnormal pineal gland', 0.45, 6.667568321314008, 1.7321679319833003, 'HP:0100547', 'Abnormal forebrain morphology'),
(404552, 'HP:0001355', 'Megalencephaly', 'XPO:0101663', 'abnormal central nervous system morphology', 0.5, 5.483278994082134, 1.6557896898583067, 'HP:0002011', 'Morphological central nervous system abnormality'),
(404553, 'HP:0001355', 'Megalencephaly', 'XPO:0139914', 'abnormally necrotic sensory system', 0.41304347826086957, 4.7814666189787065, 1.405330425021534, 'HP:0012639', 'Abnormal nervous system morphology'),
(404554, 'HP:0001355', 'Megalencephaly', 'XPO:0140831', 'abnormally necrotic dorsal thalamus', 0.40298507462686567, 6.667568321314008, 1.639185931352649, 'HP:0100547', 'Abnormal forebrain morphology'),
(404555, 'HP:0001355', 'Megalencephaly', 'XPO:0101801', 'abnormal brain morphology', 0.40350877192982454, 5.87414924076387, 1.5395683636244089, 'HP:0012443', 'Abnormal brain morphology'),
(404556, 'HP:0001355', 'Megalencephaly', 'XPO:0101895', 'abnormal prethalamus morphology', 0.43548387096774194, 6.667568321314008, 1.704000722566664, 'HP:0100547', 'Abnormal forebrain morphology'),
(404557, 'HP:0001355', 'Megalencephaly', 'XPO:0126930', 'abnormally localised subcommissural organ', 0.42857142857142855, 6.667568321314008, 1.6904228111816126, 'HP:0100547', 'Abnormal forebrain morphology'),
(404558, 'HP:0001355', 'Megalencephaly', 'XPO:0139952', 'abnormally necrotic anterior entopeduncular nucleus', 0.4142857142857143, 8.02346099791745, 1.8231854734408677, 'HP:0002060', 'Abnormal cerebral morphology'),
(404559, 'HP:0001355', 'Megalencephaly', 'XPO:0102334', 'abnormal glial cell morphology', 0.4222222222222222, 4.7814666189787065, 1.4208594094232423, 'HP:0012639', 'Abnormal nervous system morphology'),
(404560, 'HP:0001355', 'Megalencephaly', 'XPO:0101053', 'abnormal anterior hypothalamus', 0.4909090909090909, 6.667568321314008, 1.8091903999276895, 'HP:0100547', 'Abnormal forebrain morphology'),
(404561, 'HP:0001355', 'Megalencephaly', 'XPO:0139852', 'abnormally necrotic neuromere', 0.42857142857142855, 5.483278994082134, 1.5329633758669794, 'HP:0002011', 'Morphological central nervous system abnormality'),
(404562, 'HP:0001355', 'Megalencephaly', 'XPO:0130296', 'increased size of the lateral septum', 0.4084507042253521, 8.02346099791745, 1.810300608993995, 'HP:0002060', 'Abnormal cerebral morphology'),
(404563, 'HP:0001355', 'Megalencephaly', 'XPO:0139757', 'abnormally necrotic neural nucleus', 0.4375, 5.483278994082134, 1.5488494310006167, 'HP:0002011', 'Morphological central nervous system abnormality'),
(404564, 'HP:0001355', 'Megalencephaly', 'XPO:0102442', 'abnormal medial pallium morphology', 0.4915254237288136, 8.02346099791745, 1.9858839509832855, 'HP:0002060', 'Abnormal cerebral morphology'),
(404565, 'HP:0001355', 'Megalencephaly', 'XPO:0140976', 'abnormally necrotic nucleus accumbens', 0.4142857142857143, 8.02346099791745, 1.8231854734408677, 'HP:0002060', 'Abnormal cerebral morphology'),
(404566, 'HP:0001355', 'Megalencephaly', 'XPO:0140476', 'abnormally necrotic lateral ganglionic eminence', 0.4461538461538462, 8.02346099791745, 1.8920089808682852, 'HP:0002060', 'Abnormal cerebral morphology'),
(404567, 'HP:0001355', 'Megalencephaly', 'XPO:0128482', 'decreased size of the ventral pallium', 0.4393939393939394, 8.02346099791745, 1.8776208710622537, 'HP:0002060', 'Abnormal cerebral morphology'),
(404568, 'HP:0001355', 'Megalencephaly', 'XPO:0126581', 'abnormally localised prethalamus', 0.42857142857142855, 6.667568321314008, 1.6904228111816126, 'HP:0100547', 'Abnormal forebrain morphology'),
(404569, 'HP:0001355', 'Megalencephaly', 'XPO:0139938', 'abnormally necrotic prethalamus', 0.40298507462686567, 6.667568321314008, 1.639185931352649, 'HP:0100547', 'Abnormal forebrain morphology'),
(404570, 'HP:0006725', 'Pancreatic adenocarcinoma', 'XPO:0100493', 'abnormal liver and biliary system', 0.5555555555555556, 5.05060299610679, 1.6750792677938144, 'HP:0025031', 'Abnormality of the digestive system'),
(404571, 'HP:0006725', 'Pancreatic adenocarcinoma', 'XPO:0131683', 'abnormal stomach epithelium', 0.4411764705882353, 5.05060299610679, 1.4927180591674907, 'HP:0025031', 'Abnormality of the digestive system'),
(404572, 'HP:0006725', 'Pancreatic adenocarcinoma', 'XPO:0100893', 'abnormal hyoid arch', 0.42857142857142855, 5.05060299610679, 1.471238981671103, 'HP:0025031', 'Abnormality of the digestive system'),
(404573, 'HP:0006725', 'Pancreatic adenocarcinoma', 'XPO:0101297', 'abnormal barrier cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(404574, 'HP:0006725', 'Pancreatic adenocarcinoma', 'XPO:0100662', 'abnormal lung primordium', 0.40540540540540543, 5.05060299610679, 1.4309233924911664, 'HP:0025031', 'Abnormality of the digestive system'),
(404575, 'HP:0006725', 'Pancreatic adenocarcinoma', 'XPO:0100572', 'abnormal branchial arch', 0.42857142857142855, 5.05060299610679, 1.471238981671103, 'HP:0025031', 'Abnormality of the digestive system'),
(404576, 'HP:0006725', 'Pancreatic adenocarcinoma', 'XPO:0101373', 'abnormal oxygen accumulating cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(404577, 'HP:0006725', 'Pancreatic adenocarcinoma', 'XPO:0115407', 'multiple pancreases', 0.4864864864864865, 8.724209809801746, 2.060148096070132, 'HP:0001732', 'Abnormality of the pancreas'),
(404578, 'HP:0006725', 'Pancreatic adenocarcinoma', 'XPO:0100108', 'abnormal cell part', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(404579, 'HP:0006725', 'Pancreatic adenocarcinoma', 'XPO:0101333', 'abnormal barrier epithelial cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(404580, 'HP:0006725', 'Pancreatic adenocarcinoma', 'XPO:0100608', 'abnormal pancreas', 0.5, 8.724209809801746, 2.088565274273436, 'HP:0001732', 'Abnormality of the pancreas'),
(404581, 'HP:0006725', 'Pancreatic adenocarcinoma', 'XPO:0101004', 'abnormal acid secreting cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(404582, 'HP:0006725', 'Pancreatic adenocarcinoma', 'XPO:0100903', 'abnormal dorsal pancreatic bud', 0.4166666666666667, 5.05060299610679, 1.45066119926208, 'HP:0025031', 'Abnormality of the digestive system'),
(404583, 'HP:0006725', 'Pancreatic adenocarcinoma', 'XPO:0100172', 'abnormal stem cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(404584, 'HP:0006725', 'Pancreatic adenocarcinoma', 'XPO:0100986', 'abnormal gut epithelium', 0.5, 5.05060299610679, 1.5891197242666757, 'HP:0025031', 'Abnormality of the digestive system'),
(404585, 'HP:0006725', 'Pancreatic adenocarcinoma', 'XPO:0100454', 'abnormal lung bud', 0.42857142857142855, 5.05060299610679, 1.471238981671103, 'HP:0025031', 'Abnormality of the digestive system'),
(404586, 'HP:0006725', 'Pancreatic adenocarcinoma', 'XPO:0126499', 'abnormally localised liver and biliary system', 0.4166666666666667, 5.05060299610679, 1.45066119926208, 'HP:0025031', 'Abnormality of the digestive system'),
(404587, 'HP:0006725', 'Pancreatic adenocarcinoma', 'XPO:0100204', 'abnormal islets of Langerhans', 0.45, 8.724209809801746, 1.981386992591499, 'HP:0001732', 'Abnormality of the pancreas'),
(404588, 'HP:0006725', 'Pancreatic adenocarcinoma', 'XPO:0100156', 'abnormal foregut', 0.5172413793103449, 5.05060299610679, 1.6162861318637973, 'HP:0025031', 'Abnormality of the digestive system'),
(404589, 'HP:0006725', 'Pancreatic adenocarcinoma', 'XPO:0100718', 'abnormal ventral pancreatic bud', 0.4838709677419355, 5.05060299610679, 1.5632786569919361, 'HP:0025031', 'Abnormality of the digestive system'),
(404590, 'HP:0006725', 'Pancreatic adenocarcinoma', 'XPO:0100802', 'abnormal exocrine cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(404591, 'HP:0006725', 'Pancreatic adenocarcinoma', 'XPO:0100797', 'abnormal esophagus', 0.4166666666666667, 5.05060299610679, 1.45066119926208, 'HP:0025031', 'Abnormality of the digestive system'),
(404592, 'HP:0006725', 'Pancreatic adenocarcinoma', 'XPO:0126520', 'abnormally localised hindgut', 0.40540540540540543, 5.05060299610679, 1.4309233924911664, 'HP:0025031', 'Abnormality of the digestive system'),
(404593, 'HP:0006725', 'Pancreatic adenocarcinoma', 'XPO:0126466', 'abnormally localised alimentary system', 0.42857142857142855, 5.05060299610679, 1.471238981671103, 'HP:0025031', 'Abnormality of the digestive system'),
(404594, 'HP:0006725', 'Pancreatic adenocarcinoma', 'XPO:0100481', 'abnormal anatomical line', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(404595, 'HP:0006725', 'Pancreatic adenocarcinoma', 'XPO:0100533', 'abnormal melanoblast', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(404596, 'HP:0006725', 'Pancreatic adenocarcinoma', 'XPO:0142054', 'abnormal digestive tract', 0.5357142857142857, 5.05060299610679, 1.6448951870820767, 'HP:0025031', 'Abnormality of the digestive system'),
(404597, 'HP:0006725', 'Pancreatic adenocarcinoma', 'XPO:0100549', 'abnormal mitotic cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(404598, 'HP:0006725', 'Pancreatic adenocarcinoma', 'XPO:0127307', 'abnormally localised oral evagination', 0.40540540540540543, 5.05060299610679, 1.4309233924911664, 'HP:0025031', 'Abnormality of the digestive system'),
(404599, 'HP:0006725', 'Pancreatic adenocarcinoma', 'XPO:0101535', 'abnormal absorptive cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(404600, 'HP:0006725', 'Pancreatic adenocarcinoma', 'XPO:0131673', 'abnormal buccopharyngeal membrane', 0.42857142857142855, 5.05060299610679, 1.471238981671103, 'HP:0025031', 'Abnormality of the digestive system'),
(404601, 'HP:0006725', 'Pancreatic adenocarcinoma', 'XPO:0100494', 'abnormal liver diverticulum', 0.42857142857142855, 5.05060299610679, 1.471238981671103, 'HP:0025031', 'Abnormality of the digestive system'),
(404602, 'HP:0006725', 'Pancreatic adenocarcinoma', 'XPO:0101601', 'abnormal proctodeum', 0.4838709677419355, 5.05060299610679, 1.5632786569919361, 'HP:0025031', 'Abnormality of the digestive system'),
(404603, 'HP:0006725', 'Pancreatic adenocarcinoma', 'XPO:0126705', 'abnormally localised larval alimentary system', 0.40540540540540543, 5.05060299610679, 1.4309233924911664, 'HP:0025031', 'Abnormality of the digestive system'),
(404604, 'HP:0006725', 'Pancreatic adenocarcinoma', 'XPO:0100026', 'abnormal germ cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(404605, 'HP:0006725', 'Pancreatic adenocarcinoma', 'XPO:0125745', 'absent pharyngeal cavity', 0.4166666666666667, 5.05060299610679, 1.45066119926208, 'HP:0025031', 'Abnormality of the digestive system'),
(404606, 'HP:0006725', 'Pancreatic adenocarcinoma', 'XPO:0101169', 'abnormal hepato-pancreatic duct', 0.4838709677419355, 5.05060299610679, 1.5632786569919361, 'HP:0025031', 'Abnormality of the digestive system'),
(404607, 'HP:0006725', 'Pancreatic adenocarcinoma', 'XPO:0100621', 'abnormal peritoneum', 0.46875, 5.05060299610679, 1.5386585568036393, 'HP:0025031', 'Abnormality of the digestive system'),
(404608, 'HP:0006725', 'Pancreatic adenocarcinoma', 'XPO:0101784', 'abnormal alimentary system morphology', 0.4166666666666667, 5.05060299610679, 1.45066119926208, 'HP:0025031', 'Abnormality of the digestive system'),
(404609, 'HP:0006725', 'Pancreatic adenocarcinoma', 'XPO:0100006', 'abnormal anatomical structure', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(404610, 'HP:0006725', 'Pancreatic adenocarcinoma', 'XPO:0100638', 'abnormal polar body', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(404611, 'HP:0006725', 'Pancreatic adenocarcinoma', 'XPO:0101193', 'abnormal bile duct', 0.41025641025641024, 7.1173123385767045, 1.7087782216244842, 'HP:0002012', 'Abnormality of the abdominal organs'),
(404612, 'HP:0006725', 'Pancreatic adenocarcinoma', 'XPO:0107288', 'abnormal larval alimentary system', 0.5555555555555556, 5.05060299610679, 1.6750792677938144, 'HP:0025031', 'Abnormality of the digestive system'),
(404613, 'HP:0006725', 'Pancreatic adenocarcinoma', 'XPO:0100852', 'abnormal interdigital region', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(404614, 'HP:0006725', 'Pancreatic adenocarcinoma', 'XPO:0100788', 'abnormal branchial arch 4', 0.4166666666666667, 5.05060299610679, 1.45066119926208, 'HP:0025031', 'Abnormality of the digestive system'),
(404615, 'HP:0006725', 'Pancreatic adenocarcinoma', 'XPO:0101326', 'abnormal cementoblast', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(404616, 'HP:0006725', 'Pancreatic adenocarcinoma', 'XPO:0101377', 'abnormal manicotto glandulare', 0.5172413793103449, 5.05060299610679, 1.6162861318637973, 'HP:0025031', 'Abnormality of the digestive system'),
(404617, 'HP:0006725', 'Pancreatic adenocarcinoma', 'XPO:0100754', 'abnormal electrically active cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(404618, 'HP:0006725', 'Pancreatic adenocarcinoma', 'XPO:0141620', 'metaplastic pancreas', 0.46153846153846156, 8.724209809801746, 2.0066286088249243, 'HP:0001732', 'Abnormality of the pancreas'),
(404619, 'HP:0006725', 'Pancreatic adenocarcinoma', 'XPO:0100653', 'abnormal myoblast', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(404620, 'HP:0006725', 'Pancreatic adenocarcinoma', 'XPO:0100791', 'abnormal multiciliated cell precursor', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(404621, 'HP:0006725', 'Pancreatic adenocarcinoma', 'XPO:0100216', 'abnormal hepato-pancreatic progenitor cell', 0.4411764705882353, 5.05060299610679, 1.4927180591674907, 'HP:0025031', 'Abnormality of the digestive system'),
(404622, 'HP:0006725', 'Pancreatic adenocarcinoma', 'XPO:0100523', 'abnormal midgut', 0.5172413793103449, 5.05060299610679, 1.6162861318637973, 'HP:0025031', 'Abnormality of the digestive system'),
(404623, 'HP:0006725', 'Pancreatic adenocarcinoma', 'XPO:0107307', 'abnormal posterior hindgut endoderm', 0.45454545454545453, 5.05060299610679, 1.5151662069205463, 'HP:0025031', 'Abnormality of the digestive system'),
(404624, 'HP:0006725', 'Pancreatic adenocarcinoma', 'XPO:0141717', 'abnormal tracheoesophageal fold', 0.45454545454545453, 5.05060299610679, 1.5151662069205463, 'HP:0025031', 'Abnormality of the digestive system'),
(404625, 'HP:0006725', 'Pancreatic adenocarcinoma', 'XPO:0100715', 'abnormal ciliated cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(404626, 'HP:0006725', 'Pancreatic adenocarcinoma', 'XPO:0100285', 'abnormal progenitor cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(404627, 'HP:0006725', 'Pancreatic adenocarcinoma', 'XPO:0115495', 'abnormally protruding proctodeum', 0.4411764705882353, 5.05060299610679, 1.4927180591674907, 'HP:0025031', 'Abnormality of the digestive system'),
(404628, 'HP:0006725', 'Pancreatic adenocarcinoma', 'XPO:0100629', 'abnormal branchial arch 2', 0.4166666666666667, 5.05060299610679, 1.45066119926208, 'HP:0025031', 'Abnormality of the digestive system'),
(404629, 'HP:0006725', 'Pancreatic adenocarcinoma', 'XPO:0127393', 'abnormally localised pharyngeal cavity', 0.42857142857142855, 5.05060299610679, 1.471238981671103, 'HP:0025031', 'Abnormality of the digestive system'),
(404630, 'HP:0006725', 'Pancreatic adenocarcinoma', 'XPO:0100214', 'abnormal second pancreatic bud', 0.45454545454545453, 5.05060299610679, 1.5151662069205463, 'HP:0025031', 'Abnormality of the digestive system'),
(404631, 'HP:0006725', 'Pancreatic adenocarcinoma', 'XPO:0101435', 'abnormal paracrine cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(404632, 'HP:0006725', 'Pancreatic adenocarcinoma', 'XPO:0126837', 'abnormally localised midgut', 0.40540540540540543, 5.05060299610679, 1.4309233924911664, 'HP:0025031', 'Abnormality of the digestive system'),
(404633, 'HP:0006725', 'Pancreatic adenocarcinoma', 'XPO:0101237', 'abnormal mucus secreting cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(404634, 'HP:0006725', 'Pancreatic adenocarcinoma', 'XPO:0101241', 'abnormal nucleate erythrocyte', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(404635, 'HP:0006725', 'Pancreatic adenocarcinoma', 'XPO:0100344', 'abnormal portion of organism substance', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(404636, 'HP:0006725', 'Pancreatic adenocarcinoma', 'XPO:0100813', 'abnormal branchial arch 3', 0.4166666666666667, 5.05060299610679, 1.45066119926208, 'HP:0025031', 'Abnormality of the digestive system'),
(404637, 'HP:0006725', 'Pancreatic adenocarcinoma', 'XPO:0100691', 'abnormal keratin accumulating cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(404638, 'HP:0006725', 'Pancreatic adenocarcinoma', 'XPO:0100130', 'abnormal mouth primordium', 0.4411764705882353, 5.05060299610679, 1.4927180591674907, 'HP:0025031', 'Abnormality of the digestive system'),
(404639, 'HP:0006725', 'Pancreatic adenocarcinoma', 'XPO:0101467', 'abnormal alkali secreting cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(404640, 'HP:0006725', 'Pancreatic adenocarcinoma', 'XPO:0100579', 'abnormal biliary tree', 0.42105263157894735, 7.1173123385767045, 1.731116139930257, 'HP:0002012', 'Abnormality of the abdominal organs'),
(404641, 'HP:0006725', 'Pancreatic adenocarcinoma', 'XPO:0100492', 'abnormal gall bladder primordium', 0.46875, 5.05060299610679, 1.5386585568036393, 'HP:0025031', 'Abnormality of the digestive system'),
(404642, 'HP:0006725', 'Pancreatic adenocarcinoma', 'XPO:0100890', 'abnormal pharyngeal cavity', 0.5357142857142857, 5.05060299610679, 1.6448951870820767, 'HP:0025031', 'Abnormality of the digestive system'),
(404643, 'HP:0006725', 'Pancreatic adenocarcinoma', 'XPO:0102522', 'abnormal pharyngeal cavity morphology', 0.4166666666666667, 5.05060299610679, 1.45066119926208, 'HP:0025031', 'Abnormality of the digestive system'),
(404644, 'HP:0006725', 'Pancreatic adenocarcinoma', 'XPO:0101101', 'abnormal posterior foregut', 0.5, 5.05060299610679, 1.5891197242666757, 'HP:0025031', 'Abnormality of the digestive system'),
(404645, 'HP:0006725', 'Pancreatic adenocarcinoma', 'XPO:0142027', 'abnormally localised digestive tract', 0.40540540540540543, 5.05060299610679, 1.4309233924911664, 'HP:0025031', 'Abnormality of the digestive system'),
(404646, 'HP:0006725', 'Pancreatic adenocarcinoma', 'XPO:0100215', 'abnormal first pancreatic bud', 0.46875, 5.05060299610679, 1.5386585568036393, 'HP:0025031', 'Abnormality of the digestive system'),
(404647, 'HP:0006725', 'Pancreatic adenocarcinoma', 'XPO:0126608', 'abnormally localised foregut', 0.40540540540540543, 5.05060299610679, 1.4309233924911664, 'HP:0025031', 'Abnormality of the digestive system'),
(404648, 'HP:0006725', 'Pancreatic adenocarcinoma', 'XPO:0107306', 'abnormal ventral posterior hindgut endoderm', 0.4411764705882353, 5.05060299610679, 1.4927180591674907, 'HP:0025031', 'Abnormality of the digestive system'),
(404649, 'HP:0006725', 'Pancreatic adenocarcinoma', 'XPO:0101356', 'abnormal exocrine pancreas', 0.4864864864864865, 8.724209809801746, 2.060148096070132, 'HP:0001732', 'Abnormality of the pancreas'),
(404650, 'HP:0006725', 'Pancreatic adenocarcinoma', 'XPO:0100337', 'abnormal zygote', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(404651, 'HP:0006725', 'Pancreatic adenocarcinoma', 'XPO:0100591', 'abnormal pharyngeal arch', 0.4411764705882353, 5.05060299610679, 1.4927180591674907, 'HP:0025031', 'Abnormality of the digestive system'),
(404652, 'HP:0006725', 'Pancreatic adenocarcinoma', 'XPO:0100735', 'abnormal hindgut', 0.5172413793103449, 5.05060299610679, 1.6162861318637973, 'HP:0025031', 'Abnormality of the digestive system'),
(404653, 'HP:0006725', 'Pancreatic adenocarcinoma', 'XPO:0101021', 'abnormal dorsal foregut', 0.5, 5.05060299610679, 1.5891197242666757, 'HP:0025031', 'Abnormality of the digestive system'),
(404654, 'HP:0006725', 'Pancreatic adenocarcinoma', 'XPO:0124888', 'absent liver and biliary system', 0.40540540540540543, 5.05060299610679, 1.4309233924911664, 'HP:0025031', 'Abnormality of the digestive system'),
(404655, 'HP:0006725', 'Pancreatic adenocarcinoma', 'XPO:0100704', 'abnormal Merkel cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(404656, 'HP:0006725', 'Pancreatic adenocarcinoma', 'XPO:0100004', 'abnormal cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(404657, 'HP:0006725', 'Pancreatic adenocarcinoma', 'XPO:0100477', 'abnormal pericyte', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(404658, 'HP:0006725', 'Pancreatic adenocarcinoma', 'XPO:0115391', 'abnormally undifferentiated alimentary system', 0.5555555555555556, 5.05060299610679, 1.6750792677938144, 'HP:0025031', 'Abnormality of the digestive system'),
(404659, 'HP:0006725', 'Pancreatic adenocarcinoma', 'XPO:0101084', 'abnormal mesentery', 0.42857142857142855, 5.05060299610679, 1.471238981671103, 'HP:0025031', 'Abnormality of the digestive system'),
(404660, 'HP:0006725', 'Pancreatic adenocarcinoma', 'XPO:0100462', 'abnormal anterior foregut', 0.5, 5.05060299610679, 1.5891197242666757, 'HP:0025031', 'Abnormality of the digestive system'),
(404661, 'HP:0006725', 'Pancreatic adenocarcinoma', 'XPO:0100486', 'abnormal oral evagination', 0.5172413793103449, 5.05060299610679, 1.6162861318637973, 'HP:0025031', 'Abnormality of the digestive system'),
(404662, 'HP:0006725', 'Pancreatic adenocarcinoma', 'XPO:0100152', 'abnormal alimentary system', 0.5769230769230769, 5.05060299610679, 1.706988406765213, 'HP:0025031', 'Abnormality of the digestive system'),
(404663, 'HP:0006725', 'Pancreatic adenocarcinoma', 'XPO:0115392', 'abnormally incomplete structure of alimentary system', 0.40540540540540543, 5.05060299610679, 1.4309233924911664, 'HP:0025031', 'Abnormality of the digestive system'),
(404664, 'HP:0006725', 'Pancreatic adenocarcinoma', 'XPO:0101381', 'abnormal ventral foregut', 0.5, 5.05060299610679, 1.5891197242666757, 'HP:0025031', 'Abnormality of the digestive system'),
(404665, 'HP:0006725', 'Pancreatic adenocarcinoma', 'XPO:0100289', 'abnormal chondroblast', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(404666, 'HP:0006725', 'Pancreatic adenocarcinoma', 'XPO:0100081', 'abnormal anatomical entity in vitro', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(404667, 'HP:0006725', 'Pancreatic adenocarcinoma', 'XPO:0107304', 'abnormal hindgut endoderm', 0.46875, 5.05060299610679, 1.5386585568036393, 'HP:0025031', 'Abnormality of the digestive system'),
(404668, 'HP:0006725', 'Pancreatic adenocarcinoma', 'XPO:0100571', 'abnormal branchial arch 1', 0.4166666666666667, 5.05060299610679, 1.45066119926208, 'HP:0025031', 'Abnormality of the digestive system'),
(404669, 'HP:0006725', 'Pancreatic adenocarcinoma', 'XPO:0100188', 'abnormal delta cell', 0.42857142857142855, 5.05060299610679, 1.471238981671103, 'HP:0025031', 'Abnormality of the digestive system'),
(404670, 'HP:0006725', 'Pancreatic adenocarcinoma', 'XPO:0107308', 'abnormal anterior hindgut endoderm', 0.45454545454545453, 5.05060299610679, 1.5151662069205463, 'HP:0025031', 'Abnormality of the digestive system'),
(404671, 'HP:0006725', 'Pancreatic adenocarcinoma', 'XPO:0124857', 'absent alimentary system', 0.4166666666666667, 5.05060299610679, 1.45066119926208, 'HP:0025031', 'Abnormality of the digestive system'),
(404672, 'HP:0006725', 'Pancreatic adenocarcinoma', 'XPO:0131662', 'abnormal foregut epithelium', 0.4411764705882353, 5.05060299610679, 1.4927180591674907, 'HP:0025031', 'Abnormality of the digestive system'),
(404673, 'HP:0006725', 'Pancreatic adenocarcinoma', 'XPO:0101198', 'abnormal digestive enzyme secreting cell', 0.46875, 5.05060299610679, 1.5386585568036393, 'HP:0025031', 'Abnormality of the digestive system'),
(404674, 'HP:0006725', 'Pancreatic adenocarcinoma', 'XPO:0100362', 'abnormal acinar cell', 0.45, 8.724209809801746, 1.981386992591499, 'HP:0001732', 'Abnormality of the pancreas'),
(404675, 'HP:0006725', 'Pancreatic adenocarcinoma', 'XPO:0101448', 'abnormal myelin accumulating cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(404676, 'HP:0006725', 'Pancreatic adenocarcinoma', 'XPO:0101103', 'abnormal pharyngeal mesenchyme', 0.42857142857142855, 5.05060299610679, 1.471238981671103, 'HP:0025031', 'Abnormality of the digestive system'),
(404677, 'HP:0006725', 'Pancreatic adenocarcinoma', 'XPO:0107305', 'abnormal dorsal posterior hindgut endoderm', 0.4411764705882353, 5.05060299610679, 1.4927180591674907, 'HP:0025031', 'Abnormality of the digestive system'),
(404678, 'HP:0006725', 'Pancreatic adenocarcinoma', 'XPO:0101132', 'abnormal apoptotic cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(404679, 'HP:0040196', 'Mild microcephaly', 'XPO:0102052', 'abnormal choana morphology', 0.45588235294117646, 7.024697770424301, 1.78953506483714, 'HP:0000929', 'Abnormal skull morphology'),
(404680, 'HP:0040196', 'Mild microcephaly', 'XPO:0101764', 'abnormal cranium morphology', 0.43333333333333335, 4.638757693672553, 1.4177899470389728, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(404681, 'HP:0040196', 'Mild microcephaly', 'XPO:0130767', 'increased size of the orbital region', 0.41025641025641024, 7.024697770424301, 1.697624013269865, 'HP:0000929', 'Abnormal skull morphology'),
(404682, 'HP:0040196', 'Mild microcephaly', 'XPO:0128291', 'decreased size of the dermatocranium', 0.43283582089552236, 5.653868323764771, 1.564351858487059, 'UPHENO:0012541', 'decreased size of the anatomical entity in the independent continuant'),
(404683, 'HP:0040196', 'Mild microcephaly', 'XPO:0103332', 'decreased size of the chondrocranium', 0.43283582089552236, 5.653868323764771, 1.564351858487059, 'UPHENO:0012541', 'decreased size of the anatomical entity in the independent continuant'),
(404684, 'HP:0040196', 'Mild microcephaly', 'XPO:0103827', 'decreased width of the head', 0.41935483870967744, 13.457162341461329, 2.375568593662044, 'UPHENO:0069149', 'decreased size of the head'),
(404685, 'HP:0040196', 'Mild microcephaly', 'XPO:0128034', 'decreased size of the cranium', 0.453125, 5.653868323764771, 1.6005964776313584, 'UPHENO:0012541', 'decreased size of the anatomical entity in the independent continuant'),
(404686, 'HP:0040196', 'Mild microcephaly', 'XPO:0129689', 'increased size of the sphenoid region', 0.463768115942029, 7.024697770424301, 1.8049462180496818, 'HP:0000929', 'Abnormal skull morphology'),
(404687, 'HP:0040196', 'Mild microcephaly', 'XPO:0130425', 'increased size of the otic region', 0.463768115942029, 7.024697770424301, 1.8049462180496818, 'HP:0000929', 'Abnormal skull morphology'),
(404688, 'HP:0040196', 'Mild microcephaly', 'XPO:0128310', 'decreased size of the mandibular arch skeleton', 0.4142857142857143, 5.653868323764771, 1.5304629616518861, 'UPHENO:0012541', 'decreased size of the anatomical entity in the independent continuant'),
(404689, 'HP:0040196', 'Mild microcephaly', 'XPO:0102720', 'abnormal dermatocranium morphology', 0.41935483870967744, 4.638757693672553, 1.394734915474381, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(404690, 'HP:0040196', 'Mild microcephaly', 'XPO:0115586', 'abnormally decreased volume of chondrocranium', 0.42028985507246375, 5.653868323764771, 1.541513379245827, 'UPHENO:0012541', 'decreased size of the anatomical entity in the independent continuant'),
(404691, 'HP:0040196', 'Mild microcephaly', 'XPO:0129957', 'increased size of the neurocranium', 0.45714285714285713, 7.024697770424301, 1.792007368661419, 'HP:0000929', 'Abnormal skull morphology'),
(404692, 'HP:0040196', 'Mild microcephaly', 'XPO:0102828', 'abnormal occipital region morphology', 0.5, 7.024697770424301, 1.8741261657669024, 'HP:0000929', 'Abnormal skull morphology'),
(404693, 'HP:0040196', 'Mild microcephaly', 'XPO:0128209', 'decreased size of the sphenoid region', 0.5074626865671642, 7.024697770424301, 1.8880603811588983, 'HP:0000929', 'Abnormal skull morphology'),
(404694, 'HP:0040196', 'Mild microcephaly', 'XPO:0130449', 'increased size of the fenestra subocularis', 0.4153846153846154, 4.6864066944795475, 1.3952280252067308, 'UPHENO:0075195', 'abnormal size of anatomical entity'),
(404695, 'HP:0040196', 'Mild microcephaly', 'XPO:0140644', 'abnormally necrotic otic region', 0.45588235294117646, 7.024697770424301, 1.78953506483714, 'HP:0000929', 'Abnormal skull morphology'),
(404696, 'HP:0040196', 'Mild microcephaly', 'XPO:0128668', 'decreased size of the fenestra basicranialis', 0.4603174603174603, 5.653868323764771, 1.6132496111156314, 'UPHENO:0012541', 'decreased size of the anatomical entity in the independent continuant'),
(404697, 'HP:0040196', 'Mild microcephaly', 'XPO:0130324', 'increased size of the choana', 0.4383561643835616, 7.024697770424301, 1.7547990114531504, 'HP:0000929', 'Abnormal skull morphology'),
(404698, 'HP:0040196', 'Mild microcephaly', 'XPO:0128905', 'decreased size of the occipital region', 0.5151515151515151, 7.024697770424301, 1.902310095624672, 'HP:0000929', 'Abnormal skull morphology'),
(404699, 'HP:0040196', 'Mild microcephaly', 'XPO:0102776', 'abnormal fenestra subocularis morphology', 0.4262295081967213, 4.638757693672553, 1.4061206955371255, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(404700, 'HP:0040196', 'Mild microcephaly', 'XPO:0128582', 'decreased size of the head region', 0.41379310344827586, 5.653868323764771, 1.529552784371473, 'UPHENO:0012541', 'decreased size of the anatomical entity in the independent continuant'),
(404701, 'HP:0040196', 'Mild microcephaly', 'XPO:0128971', 'decreased size of the fenestra subocularis', 0.4603174603174603, 5.653868323764771, 1.6132496111156314, 'UPHENO:0012541', 'decreased size of the anatomical entity in the independent continuant'),
(404702, 'HP:0040196', 'Mild microcephaly', 'XPO:0102005', 'abnormal splanchnocranium morphology', 0.41935483870967744, 4.638757693672553, 1.394734915474381, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(404703, 'HP:0040196', 'Mild microcephaly', 'XPO:0140926', 'abnormally necrotic neurocranium', 0.45588235294117646, 7.024697770424301, 1.78953506483714, 'HP:0000929', 'Abnormal skull morphology'),
(404704, 'HP:0040196', 'Mild microcephaly', 'XPO:0103574', 'decreased length of notochord', 0.4126984126984127, 8.382327108538739, 1.8599390023365854, 'UPHENO:0031839', 'decreased length of anatomical entity in independent continuant'),
(404705, 'HP:0040196', 'Mild microcephaly', 'XPO:0128033', 'decreased size of the splanchnocranium', 0.43283582089552236, 5.653868323764771, 1.564351858487059, 'UPHENO:0012541', 'decreased size of the anatomical entity in the independent continuant'),
(404706, 'HP:0040196', 'Mild microcephaly', 'XPO:0128880', 'decreased size of the lower jaw', 0.41975308641975306, 7.024697770424301, 1.717160030486838, 'HP:0000929', 'Abnormal skull morphology'),
(404707, 'HP:0040196', 'Mild microcephaly', 'XPO:0131600', 'decreased size of the intercanthal region', 0.41379310344827586, 5.653868323764771, 1.529552784371473, 'UPHENO:0012541', 'decreased size of the anatomical entity in the independent continuant'),
(404708, 'HP:0040196', 'Mild microcephaly', 'XPO:0102564', 'abnormal olfactory region morphology', 0.49206349206349204, 7.024697770424301, 1.8591926515575539, 'HP:0000929', 'Abnormal skull morphology'),
(404709, 'HP:0040196', 'Mild microcephaly', 'XPO:0129406', 'decreased size of the suspensorium', 0.4393939393939394, 5.653868323764771, 1.5761584551032968, 'UPHENO:0012541', 'decreased size of the anatomical entity in the independent continuant'),
(404710, 'HP:0040196', 'Mild microcephaly', 'XPO:0140672', 'abnormally necrotic olfactory region', 0.45588235294117646, 7.024697770424301, 1.78953506483714, 'HP:0000929', 'Abnormal skull morphology'),
(404711, 'HP:0040196', 'Mild microcephaly', 'XPO:0102401', 'abnormal neurocranium morphology', 0.49206349206349204, 7.024697770424301, 1.8591926515575539, 'HP:0000929', 'Abnormal skull morphology'),
(404712, 'HP:0040196', 'Mild microcephaly', 'XPO:0103381', 'increased size of the head', 0.5645161290322581, 13.167655724266345, 2.7264178032525193, 'UPHENO:0075220', 'abnormal size of skull'),
(404713, 'HP:0040196', 'Mild microcephaly', 'XPO:0129688', 'increased size of the olfactory region', 0.463768115942029, 7.024697770424301, 1.8049462180496818, 'HP:0000929', 'Abnormal skull morphology'),
(404714, 'HP:0040196', 'Mild microcephaly', 'XPO:0128208', 'decreased size of the olfactory region', 0.5074626865671642, 7.024697770424301, 1.8880603811588983, 'HP:0000929', 'Abnormal skull morphology'),
(404715, 'HP:0040196', 'Mild microcephaly', 'XPO:0130383', 'increased size of the occipital region', 0.47058823529411764, 7.024697770424301, 1.8181694440448872, 'HP:0000929', 'Abnormal skull morphology'),
(404716, 'HP:0040196', 'Mild microcephaly', 'XPO:0141201', 'abnormally necrotic sphenoid region', 0.45588235294117646, 7.024697770424301, 1.78953506483714, 'HP:0000929', 'Abnormal skull morphology'),
(404717, 'HP:0040196', 'Mild microcephaly', 'XPO:0129718', 'increased size of the ethmoid region', 0.40298507462686567, 4.6864066944795475, 1.3742459574278119, 'UPHENO:0075195', 'abnormal size of anatomical entity'),
(404718, 'HP:0040196', 'Mild microcephaly', 'XPO:0129225', 'decreased size of the upper jaw', 0.40963855421686746, 7.024697770424301, 1.696345200272357, 'HP:0000929', 'Abnormal skull morphology'),
(404719, 'HP:0040196', 'Mild microcephaly', 'XPO:0128659', 'decreased size of the braincase and otic capsule skeleton', 0.42028985507246375, 5.653868323764771, 1.541513379245827, 'UPHENO:0012541', 'decreased size of the anatomical entity in the independent continuant'),
(404720, 'HP:0040196', 'Mild microcephaly', 'XPO:0103176', 'abnormal fenestra basicranialis morphology', 0.4262295081967213, 4.638757693672553, 1.4061206955371255, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(404721, 'HP:0040196', 'Mild microcephaly', 'XPO:0130147', 'increased size of the fenestra basicranialis', 0.4153846153846154, 4.6864066944795475, 1.3952280252067308, 'UPHENO:0075195', 'abnormal size of anatomical entity'),
(404722, 'HP:0040196', 'Mild microcephaly', 'XPO:0102665', 'abnormal suspensorium morphology', 0.41935483870967744, 4.638757693672553, 1.394734915474381, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(404723, 'HP:0040196', 'Mild microcephaly', 'XPO:0128947', 'decreased size of the otic region', 0.5074626865671642, 7.024697770424301, 1.8880603811588983, 'HP:0000929', 'Abnormal skull morphology'),
(404724, 'HP:0040196', 'Mild microcephaly', 'XPO:0141829', 'increased width of head', 0.5303030303030303, 13.167655724266345, 2.6425078491019636, 'HP:0000240', 'Abnormality of skull size'),
(404725, 'HP:0040196', 'Mild microcephaly', 'XPO:0101659', 'abnormal lower jaw morphology', 0.4025974025974026, 7.024697770424301, 1.6817030286006471, 'HP:0000929', 'Abnormal skull morphology'),
(404726, 'HP:0040196', 'Mild microcephaly', 'XPO:0128238', 'decreased size of the ethmoid region', 0.4461538461538462, 5.653868323764771, 1.58823647429942, 'UPHENO:0012541', 'decreased size of the anatomical entity in the independent continuant'),
(404727, 'HP:0040196', 'Mild microcephaly', 'XPO:0102092', 'abnormal ethmoid region morphology', 0.4262295081967213, 4.638757693672553, 1.4061206955371255, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(404728, 'HP:0040196', 'Mild microcephaly', 'XPO:0103342', 'decreased size of the head', 0.4482758620689655, 13.457162341461329, 2.456119103305171, 'UPHENO:0069149', 'decreased size of the head'),
(404729, 'HP:0040196', 'Mild microcephaly', 'XPO:0128846', 'decreased size of the choana', 0.4788732394366197, 7.024697770424301, 1.8341046255288396, 'HP:0000929', 'Abnormal skull morphology'),
(404730, 'HP:0040196', 'Mild microcephaly', 'XPO:0103358', 'decreased size of the pharyngeal region', 0.43636363636363634, 5.653868323764771, 1.570714022754993, 'UPHENO:0012541', 'decreased size of the anatomical entity in the independent continuant'),
(404731, 'HP:0040196', 'Mild microcephaly', 'XPO:0141185', 'abnormally necrotic occipital region', 0.4626865671641791, 7.024697770424301, 1.8028403414510898, 'HP:0000929', 'Abnormal skull morphology'),
(404732, 'HP:0040196', 'Mild microcephaly', 'XPO:0103152', 'abnormal otic region morphology', 0.49206349206349204, 7.024697770424301, 1.8591926515575539, 'HP:0000929', 'Abnormal skull morphology'),
(404733, 'HP:0040196', 'Mild microcephaly', 'XPO:0101997', 'abnormal braincase and otic capsule skeleton morphology', 0.40625, 4.638757693672553, 1.3727692133255593, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(404734, 'HP:0040196', 'Mild microcephaly', 'XPO:0129514', 'increased size of the cranium', 0.4090909090909091, 4.6864066944795475, 1.3846177721719306, 'UPHENO:0075195', 'abnormal size of anatomical entity'),
(404735, 'HP:0040196', 'Mild microcephaly', 'XPO:0129291', 'decreased size of the orbital region', 0.4473684210526316, 7.024697770424301, 1.7727458785530037, 'HP:0000929', 'Abnormal skull morphology'),
(404736, 'HP:0040196', 'Mild microcephaly', 'XPO:0102351', 'abnormal sphenoid region morphology', 0.49206349206349204, 7.024697770424301, 1.8591926515575539, 'HP:0000929', 'Abnormal skull morphology'),
(404737, 'HP:0040196', 'Mild microcephaly', 'XPO:0140560', 'abnormally necrotic orbital region', 0.41333333333333333, 7.024697770424301, 1.7039782114536297, 'HP:0000929', 'Abnormal skull morphology'),
(404738, 'HP:0040196', 'Mild microcephaly', 'XPO:0102921', 'abnormal orbital region morphology', 0.44285714285714284, 7.024697770424301, 1.7637850163909, 'HP:0000929', 'Abnormal skull morphology'),
(404739, 'HP:0040196', 'Mild microcephaly', 'XPO:0101681', 'abnormal chondrocranium morphology', 0.41935483870967744, 4.638757693672553, 1.394734915474381, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(404740, 'HP:0040196', 'Mild microcephaly', 'XPO:0128477', 'decreased size of the neurocranium', 0.5, 7.024697770424301, 1.8741261657669024, 'HP:0000929', 'Abnormal skull morphology'),
(404741, 'HP:0033599', 'Glomerular amyloid subepithelial deposits', 'XPO:0140005', 'abnormally necrotic glomus', 0.4931506849315068, 9.777421615988073, 2.195846571777873, 'HP:0000095', 'Abnormal renal glomerulus morphology'),
(404742, 'HP:0033599', 'Glomerular amyloid subepithelial deposits', 'XPO:0102582', 'abnormal pronephric nephron morphology', 0.4264705882352941, 8.69044940390107, 1.9251548169720663, 'UPHENO:0076756', 'abnormal nephron morphology'),
(404743, 'HP:0033599', 'Glomerular amyloid subepithelial deposits', 'XPO:0103121', 'abnormal mesonephric late proximal tubule morphology', 0.4027777777777778, 8.69044940390107, 1.8709141879823046, 'UPHENO:0076756', 'abnormal nephron morphology'),
(404744, 'HP:0033599', 'Glomerular amyloid subepithelial deposits', 'XPO:0102879', 'abnormal mesonephric early proximal tubule morphology', 0.4027777777777778, 8.69044940390107, 1.8709141879823046, 'UPHENO:0076756', 'abnormal nephron morphology'),
(404745, 'HP:0033599', 'Glomerular amyloid subepithelial deposits', 'XPO:0129279', 'decreased size of the glomerulus', 0.5, 9.777421615988073, 2.2110429231460063, 'HP:0000095', 'Abnormal renal glomerulus morphology'),
(404746, 'HP:0033599', 'Glomerular amyloid subepithelial deposits', 'XPO:0140478', 'abnormally necrotic glomerulus', 0.5142857142857142, 9.777421615988073, 2.2424068006610685, 'HP:0000095', 'Abnormal renal glomerulus morphology'),
(404747, 'HP:0033599', 'Glomerular amyloid subepithelial deposits', 'XPO:0103061', 'abnormal glomerular mesangial cell morphology', 0.48, 9.777421615988073, 2.166370784439791, 'HP:0000095', 'Abnormal renal glomerulus morphology'),
(404748, 'HP:0033599', 'Glomerular amyloid subepithelial deposits', 'XPO:0141643', 'neoplastic kidney', 0.4262295081967213, 7.603795021646889, 1.800267150315539, 'HP:0012210', 'Abnormal renal morphology'),
(404749, 'HP:0033599', 'Glomerular amyloid subepithelial deposits', 'XPO:0128865', 'decreased size of the glomerular mesangial cell', 0.4090909090909091, 9.777421615988073, 1.9999635740307038, 'HP:0000095', 'Abnormal renal glomerulus morphology'),
(404750, 'HP:0033599', 'Glomerular amyloid subepithelial deposits', 'XPO:0130613', 'increased size of the glomeral nexus', 0.46153846153846156, 9.777421615988073, 2.124301327603039, 'HP:0000095', 'Abnormal renal glomerulus morphology'),
(404751, 'HP:0033599', 'Glomerular amyloid subepithelial deposits', 'XPO:0129967', 'increased size of the podocyte', 0.4235294117647059, 9.777421615988073, 2.034951013070081, 'HP:0000095', 'Abnormal renal glomerulus morphology'),
(404752, 'HP:0033599', 'Glomerular amyloid subepithelial deposits', 'XPO:0101902', 'abnormal mesonephric tubule morphology', 0.4142857142857143, 8.69044940390107, 1.897453303446231, 'UPHENO:0076756', 'abnormal nephron morphology'),
(404753, 'HP:0033599', 'Glomerular amyloid subepithelial deposits', 'XPO:0140802', 'abnormally necrotic glomerular mesangial cell', 0.45, 9.777421615988073, 2.097579492461402, 'HP:0000095', 'Abnormal renal glomerulus morphology'),
(404754, 'HP:0033599', 'Glomerular amyloid subepithelial deposits', 'XPO:0102743', 'abnormal mesonephric late distal tubule morphology', 0.4027777777777778, 8.69044940390107, 1.8709141879823046, 'UPHENO:0076756', 'abnormal nephron morphology'),
(404755, 'HP:0033599', 'Glomerular amyloid subepithelial deposits', 'XPO:0128487', 'decreased size of the podocyte', 0.4235294117647059, 9.777421615988073, 2.034951013070081, 'HP:0000095', 'Abnormal renal glomerulus morphology'),
(404756, 'HP:0033599', 'Glomerular amyloid subepithelial deposits', 'XPO:0107387', 'abnormal embryonic kidney morphology', 0.43333333333333335, 7.603795021646889, 1.8152073828391213, 'HP:0012210', 'Abnormal renal morphology'),
(404757, 'HP:0033599', 'Glomerular amyloid subepithelial deposits', 'XPO:0103197', 'abnormal mesonephric early distal tubule morphology', 0.4027777777777778, 8.69044940390107, 1.8709141879823046, 'UPHENO:0076756', 'abnormal nephron morphology'),
(404758, 'HP:0033599', 'Glomerular amyloid subepithelial deposits', 'XPO:0101717', 'abnormal mesonephric sinus morphology', 0.5098039215686274, 7.603795021646889, 1.9688688429754762, 'HP:0012210', 'Abnormal renal morphology'),
(404759, 'HP:0033599', 'Glomerular amyloid subepithelial deposits', 'XPO:0130678', 'increased size of the mesonephric sinus', 0.4642857142857143, 7.603795021646889, 1.8789181469418736, 'HP:0012210', 'Abnormal renal morphology'),
(404760, 'HP:0033599', 'Glomerular amyloid subepithelial deposits', 'XPO:0141107', 'abnormally necrotic glomerular epithelial cell', 0.43902439024390244, 9.777421615988073, 2.0718413460293514, 'HP:0000095', 'Abnormal renal glomerulus morphology'),
(404761, 'HP:0033599', 'Glomerular amyloid subepithelial deposits', 'XPO:0130755', 'increased size of the glomerulus', 0.4864864864864865, 9.777421615988073, 2.1809593047232823, 'HP:0000095', 'Abnormal renal glomerulus morphology'),
(404762, 'HP:0033599', 'Glomerular amyloid subepithelial deposits', 'XPO:0107388', 'abnormal adult kidney morphology', 0.43333333333333335, 7.603795021646889, 1.8152073828391213, 'HP:0012210', 'Abnormal renal morphology'),
(404763, 'HP:0033599', 'Glomerular amyloid subepithelial deposits', 'XPO:0102040', 'abnormal glomus morphology', 0.5294117647058824, 9.777421615988073, 2.275144398053382, 'HP:0000095', 'Abnormal renal glomerulus morphology'),
(404764, 'HP:0033599', 'Glomerular amyloid subepithelial deposits', 'XPO:0129781', 'increased size of the glomus', 0.4675324675324675, 9.777421615988073, 2.1380509943002273, 'HP:0000095', 'Abnormal renal glomerulus morphology'),
(404765, 'HP:0033599', 'Glomerular amyloid subepithelial deposits', 'XPO:0129137', 'decreased size of the glomeral nexus', 0.46153846153846156, 9.777421615988073, 2.124301327603039, 'HP:0000095', 'Abnormal renal glomerulus morphology'),
(404766, 'HP:0033599', 'Glomerular amyloid subepithelial deposits', 'XPO:0140127', 'abnormally necrotic podocyte', 0.4675324675324675, 9.777421615988073, 2.1380509943002273, 'HP:0000095', 'Abnormal renal glomerulus morphology'),
(404767, 'HP:0033599', 'Glomerular amyloid subepithelial deposits', 'XPO:0129202', 'decreased size of the mesonephric sinus', 0.4642857142857143, 7.603795021646889, 1.8789181469418736, 'HP:0012210', 'Abnormal renal morphology'),
(404768, 'HP:0033599', 'Glomerular amyloid subepithelial deposits', 'XPO:0139909', 'abnormally necrotic mesonephric nephron', 0.4142857142857143, 8.69044940390107, 1.897453303446231, 'UPHENO:0076756', 'abnormal nephron morphology'),
(404769, 'HP:0033599', 'Glomerular amyloid subepithelial deposits', 'XPO:0102837', 'abnormal glomerular epithelial cell morphology', 0.4675324675324675, 9.777421615988073, 2.1380509943002273, 'HP:0000095', 'Abnormal renal glomerulus morphology'),
(404770, 'HP:0033599', 'Glomerular amyloid subepithelial deposits', 'XPO:0139856', 'abnormally necrotic glomeral nexus', 0.4675324675324675, 9.777421615988073, 2.1380509943002273, 'HP:0000095', 'Abnormal renal glomerulus morphology'),
(404771, 'HP:0033599', 'Glomerular amyloid subepithelial deposits', 'XPO:0101779', 'abnormal mesonephric mesenchyme morphology', 0.4406779661016949, 7.603795021646889, 1.8305258601815884, 'HP:0012210', 'Abnormal renal morphology'),
(404772, 'HP:0033599', 'Glomerular amyloid subepithelial deposits', 'XPO:0102198', 'abnormal kidney morphology', 0.4482758620689655, 7.603795021646889, 1.8462388167093844, 'HP:0012210', 'Abnormal renal morphology'),
(404773, 'HP:0033599', 'Glomerular amyloid subepithelial deposits', 'XPO:0102671', 'abnormal glomeral nexus morphology', 0.5070422535211268, 9.777421615988073, 2.226559204197537, 'HP:0000095', 'Abnormal renal glomerulus morphology'),
(404774, 'HP:0033599', 'Glomerular amyloid subepithelial deposits', 'XPO:0128159', 'decreased size of the mesonephric nephron', 0.4084507042253521, 8.69044940390107, 1.8840435714330452, 'UPHENO:0076756', 'abnormal nephron morphology'),
(404775, 'HP:0033599', 'Glomerular amyloid subepithelial deposits', 'XPO:0129639', 'increased size of the mesonephric nephron', 0.4084507042253521, 8.69044940390107, 1.8840435714330452, 'UPHENO:0076756', 'abnormal nephron morphology'),
(404776, 'HP:0033599', 'Glomerular amyloid subepithelial deposits', 'XPO:0130343', 'increased size of the glomerular mesangial cell', 0.4090909090909091, 9.777421615988073, 1.9999635740307038, 'HP:0000095', 'Abnormal renal glomerulus morphology'),
(404777, 'HP:0033599', 'Glomerular amyloid subepithelial deposits', 'XPO:0102909', 'abnormal glomerulus morphology', 0.5538461538461539, 9.777421615988073, 2.3270555121327123, 'HP:0000095', 'Abnormal renal glomerulus morphology'),
(404778, 'HP:0033599', 'Glomerular amyloid subepithelial deposits', 'XPO:0103049', 'abnormal podocyte morphology', 0.4931506849315068, 9.777421615988073, 2.195846571777873, 'HP:0000095', 'Abnormal renal glomerulus morphology'),
(404779, 'HP:0033599', 'Glomerular amyloid subepithelial deposits', 'XPO:0128301', 'decreased size of the glomus', 0.48, 9.777421615988073, 2.166370784439791, 'HP:0000095', 'Abnormal renal glomerulus morphology'),
(404780, 'HP:0033599', 'Glomerular amyloid subepithelial deposits', 'XPO:0101903', 'abnormal mesonephric nephron morphology', 0.453125, 8.69044940390107, 1.9844041640106163, 'UPHENO:0076756', 'abnormal nephron morphology'),
(404781, 'HP:0000457', 'Depressed nasal ridge', 'XPO:0127898', 'abnormally localised nostril', 0.4393939393939394, 9.601025046317446, 2.053930918342022, 'UPHENO:0021517', 'abnormal nose morphology'),
(404782, 'HP:0000457', 'Depressed nasal ridge', 'XPO:0103115', 'abnormal nostril morphology', 0.453125, 9.601025046317446, 2.0857767076349742, 'UPHENO:0021517', 'abnormal nose morphology'),
(404783, 'HP:0000457', 'Depressed nasal ridge', 'XPO:0125246', 'absent choana', 0.4142857142857143, 9.601025046317446, 1.9943839949188964, 'UPHENO:0021517', 'abnormal nose morphology'),
(404784, 'HP:0000457', 'Depressed nasal ridge', 'XPO:0101483', 'abnormal nostril', 0.5178571428571429, 9.601025046317446, 2.2297890929381237, 'UPHENO:0021517', 'abnormal nose morphology'),
(404785, 'HP:0000457', 'Depressed nasal ridge', 'XPO:0102226', 'abnormal Jacobsons organ morphology', 0.4153846153846154, 9.467216006125252, 1.9830622480062023, 'UPHENO:0087950', 'abnormal nose morphology'),
(404786, 'HP:0000457', 'Depressed nasal ridge', 'XPO:0133370', 'olfactory pit fused with brain', 0.4090909090909091, 9.467216006125252, 1.967981707868695, 'UPHENO:0087950', 'abnormal nose morphology'),
(404787, 'HP:0000457', 'Depressed nasal ridge', 'XPO:0126871', 'abnormally localised choana', 0.4461538461538462, 9.601025046317446, 2.0696700827508563, 'UPHENO:0021517', 'abnormal nose morphology'),
(404788, 'HP:0000457', 'Depressed nasal ridge', 'XPO:0102966', 'abnormal olfactory pit morphology', 0.42857142857142855, 9.467216006125252, 2.01429349607732, 'UPHENO:0087950', 'abnormal nose morphology'),
(404789, 'HP:0000457', 'Depressed nasal ridge', 'XPO:0100420', 'abnormal choana', 0.5, 9.601025046317446, 2.191007193771559, 'UPHENO:0021517', 'abnormal nose morphology'),
(404790, 'HP:0000457', 'Depressed nasal ridge', 'XPO:0102052', 'abnormal choana morphology', 0.4084507042253521, 9.601025046317446, 1.9802892317673206, 'UPHENO:0021517', 'abnormal nose morphology'),
(404791, 'HP:0000457', 'Depressed nasal ridge', 'XPO:0126234', 'absent nostril', 0.4084507042253521, 9.601025046317446, 1.9802892317673206, 'UPHENO:0021517', 'abnormal nose morphology'),
(404792, 'HP:0000506', 'Telecanthus', 'XPO:0102657', 'abnormal conjunctiva morphology', 0.4189189189189189, 9.23763525381927, 1.9671858513870166, 'HP:0030669', 'Abnormal ocular adnexa morphology'),
(404793, 'HP:0000506', 'Telecanthus', 'XPO:0115526', 'abnormally incomplete structure of head', 0.40384615384615385, 4.5318002188002176, 1.3528303989641963, 'UPHENO:0087907', 'abnormal head morphology'),
(404794, 'HP:0000506', 'Telecanthus', 'XPO:0100371', 'abnormal hyaloid blood vessel', 0.4153846153846154, 6.575878401988876, 1.652730686114997, 'UPHENO:0087924', 'abnormal camera-type eye morphology'),
(404795, 'HP:0000506', 'Telecanthus', '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'),
(404796, 'HP:0000506', 'Telecanthus', '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'),
(404797, 'HP:0000506', 'Telecanthus', 'XPO:0129658', 'increased size of the conjunctiva', 0.4358974358974359, 9.23763525381927, 2.0066543102626273, 'HP:0030669', 'Abnormal ocular adnexa morphology'),
(404798, 'HP:0000506', 'Telecanthus', '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'),
(404799, 'HP:0000506', 'Telecanthus', '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'),
(404800, 'HP:0000506', 'Telecanthus', 'XPO:0102259', 'abnormal pharyngeal region morphology', 0.42, 4.5318002188002176, 1.3796217205799897, 'UPHENO:0087907', 'abnormal head morphology'),
(404801, 'HP:0000506', 'Telecanthus', 'XPO:0129212', 'decreased size of the lower eyelid', 0.44155844155844154, 10.252047911556717, 2.12764618736515, 'HP:0000492', 'Abnormal eyelid morphology'),
(404802, 'HP:0000506', 'Telecanthus', 'XPO:0102831', 'abnormal optic disc morphology', 0.4090909090909091, 6.575878401988876, 1.640162209521029, 'UPHENO:0087924', 'abnormal camera-type eye morphology'),
(404803, 'HP:0000506', 'Telecanthus', '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'),
(404804, 'HP:0000506', 'Telecanthus', 'XPO:0140547', 'abnormally necrotic lower eyelid', 0.4342105263157895, 10.252047911556717, 2.1098689815938174, 'HP:0000492', 'Abnormal eyelid morphology'),
(404805, 'HP:0000506', 'Telecanthus', 'XPO:0101483', 'abnormal nostril', 0.42105263157894735, 5.788671267106304, 1.561196743002159, 'UPHENO:0087472', 'abnormal face morphology'),
(404806, 'HP:0000506', 'Telecanthus', 'XPO:0100420', 'abnormal choana', 0.4067796610169492, 5.788671267106304, 1.5345076525622334, 'UPHENO:0087472', 'abnormal face morphology'),
(404807, 'HP:0000506', 'Telecanthus', 'XPO:0130048', 'increased size of the optic disc', 0.4411764705882353, 6.575878401988876, 1.7032682772854242, 'UPHENO:0087924', 'abnormal camera-type eye morphology'),
(404808, 'HP:0000506', 'Telecanthus', 'XPO:0100710', 'abnormal hyaloid vein', 0.40298507462686567, 6.575878401988876, 1.6278761772821302, 'UPHENO:0087924', 'abnormal camera-type eye morphology'),
(404809, 'HP:0000506', 'Telecanthus', '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'),
(404810, 'HP:0000506', 'Telecanthus', 'XPO:0100779', 'abnormal optic choroid vascular plexus', 0.4090909090909091, 6.575878401988876, 1.640162209521029, 'UPHENO:0087924', 'abnormal camera-type eye morphology'),
(404811, 'HP:0000506', 'Telecanthus', 'XPO:0130859', 'increased size of the globe', 0.4166666666666667, 6.575878401988876, 1.6552792314778892, 'UPHENO:0087924', 'abnormal camera-type eye morphology'),
(404812, 'HP:0000506', 'Telecanthus', 'XPO:0141839', 'edematous pharyngeal region', 0.40384615384615385, 4.5318002188002176, 1.3528303989641963, 'UPHENO:0087907', 'abnormal head morphology'),
(404813, 'HP:0000506', 'Telecanthus', 'XPO:0103358', 'decreased size of the pharyngeal region', 0.4074074074074074, 4.6864066944795475, 1.3817658272857345, 'UPHENO:0075195', 'abnormal size of anatomical entity'),
(404814, 'HP:0000506', 'Telecanthus', 'XPO:0102723', 'abnormal lower eyelid morphology', 0.4714285714285714, 10.252047911556717, 2.198433146848558, 'HP:0000492', 'Abnormal eyelid morphology'),
(404815, 'HP:0000506', 'Telecanthus', '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'),
(404816, 'HP:0000506', 'Telecanthus', 'XPO:0101315', 'abnormal hyaloid vascular plexus', 0.40298507462686567, 6.575878401988876, 1.6278761772821302, 'UPHENO:0087924', 'abnormal camera-type eye morphology'),
(404817, 'HP:0000506', 'Telecanthus', 'XPO:0101634', 'abnormal head morphology', 0.4117647058823529, 4.5318002188002176, 1.3660290568695288, 'UPHENO:0087907', 'abnormal head morphology'),
(404818, 'HP:0000506', 'Telecanthus', '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'),
(404819, 'HP:0000506', 'Telecanthus', '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'),
(404820, 'HP:0000506', 'Telecanthus', 'XPO:0130396', 'increased size of the choroid', 0.40540540540540543, 6.575878401988876, 1.6327573761753305, 'UPHENO:0087924', 'abnormal camera-type eye morphology'),
(404821, 'HP:0000506', 'Telecanthus', 'XPO:0130688', 'increased size of the lower eyelid', 0.48, 10.252047911556717, 2.218328874974859, 'HP:0000492', 'Abnormal eyelid morphology'),
(404822, 'HP:0000506', 'Telecanthus', 'XPO:0142059', 'abnormal nasal region morphology', 0.40384615384615385, 4.5318002188002176, 1.3528303989641963, 'UPHENO:0087907', 'abnormal head morphology'),
(404823, 'HP:0000506', 'Telecanthus', 'XPO:0130079', 'increased size of the olfactory pit', 0.421875, 5.972749669260594, 1.5873732285506497, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(404824, 'HP:0004214', 'Curved phalanges of the 5th finger', 'XPO:0103634', 'abnormally increased number of forelimb digit', 0.4222222222222222, 7.774297771301195, 1.811761927300621, 'HP:0005918', 'Abnormal finger phalanx morphology'),
(404825, 'HP:0004214', 'Curved phalanges of the 5th finger', 'XPO:0103609', 'abnormally increased number of forelimb digit in the regenerating forelimb', 0.40425531914893614, 7.774297771301195, 1.7727947503014068, 'HP:0005918', 'Abnormal finger phalanx morphology'),
(404826, 'HP:0009521', 'Small epiphysis of the middle phalanx of the 2nd finger', 'XPO:0103634', 'abnormally increased number of forelimb digit', 0.4014084507042254, 7.774297771301195, 1.7665414865468982, 'HP:0005918', 'Abnormal finger phalanx morphology'),
(404827, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0100987', 'abnormal larval aorta', 0.5161290322580645, 5.809304221129108, 1.731574591446772, 'UPHENO:0002678', 'abnormal vasculature'),
(404828, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0100232', 'abnormal lymphatic system', 0.52, 5.64885357140806, 1.713885602113569, 'HP:0002715', 'Abnormality of the immune system'),
(404829, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0101330', 'abnormal postcaval vein', 0.4444444444444444, 5.809304221129108, 1.6068332169732154, 'UPHENO:0002678', 'abnormal vasculature'),
(404830, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0101525', 'abnormal posterior vena cava', 0.4444444444444444, 5.809304221129108, 1.6068332169732154, 'UPHENO:0002678', 'abnormal vasculature'),
(404831, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0100659', 'abnormal anterior cardinal vein', 0.5, 5.809304221129108, 1.7043039959363335, 'UPHENO:0002678', 'abnormal vasculature'),
(404832, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0125889', 'absent ventral caudal lymphatic vessel', 0.4318181818181818, 8.696350005340756, 1.9378446913415897, 'HP:0100763', 'Abnormality of the lymphatic system'),
(404833, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0100076', 'abnormal artery', 0.5333333333333333, 5.809304221129108, 1.760197598169646, 'UPHENO:0002678', 'abnormal vasculature'),
(404834, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0100922', 'abnormal lymph vessel', 0.6129032258064516, 8.696350005340756, 2.308683817896098, 'HP:0100763', 'Abnormality of the lymphatic system'),
(404835, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0100907', 'abnormal cytoplasm', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(404836, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0100981', 'abnormal dorsal longitudinal anastomosing vessel', 0.5333333333333333, 5.809304221129108, 1.760197598169646, 'UPHENO:0002678', 'abnormal vasculature'),
(404837, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0100081', 'abnormal anatomical entity in vitro', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(404838, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0101547', 'abnormal lampbrush chromosome', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(404839, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0141626', 'metaplastic spleen', 0.40425531914893614, 8.696350005340756, 1.8749788657048592, 'HP:0100763', 'Abnormality of the lymphatic system'),
(404840, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0100724', 'abnormal kinetochore', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(404841, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0100429', 'abnormal spermatid', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(404842, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0100980', 'abnormal dorsal longitudinal anastomosing vessel - left branch', 0.5161290322580645, 5.809304221129108, 1.731574591446772, 'UPHENO:0002678', 'abnormal vasculature'),
(404843, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0115758', 'abnormally decreased mobility of melanoblast', 0.41379310344827586, 2.13901709234296, 0.9408031255100615, 'UPHENO:0075696', 'abnormal anatomical entity'),
(404844, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0100504', 'abnormal renal artery', 0.41025641025641024, 5.809304221129108, 1.5437954190396599, 'UPHENO:0002678', 'abnormal vasculature'),
(404845, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0100715', 'abnormal ciliated cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(404846, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0124762', 'absent blood vessel', 0.42105263157894735, 5.809304221129108, 1.5639766078650594, 'UPHENO:0002678', 'abnormal vasculature'),
(404847, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0101272', 'abnormal lateral abdominal vein', 0.4444444444444444, 5.809304221129108, 1.6068332169732154, 'UPHENO:0002678', 'abnormal vasculature'),
(404848, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0101237', 'abnormal mucus secreting cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(404849, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0100258', 'abnormal organ part', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(404850, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0101297', 'abnormal barrier cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(404851, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0126677', 'abnormally localised dorsal lymph space', 0.42424242424242425, 5.64885357140806, 1.548057923116778, 'HP:0002715', 'Abnormality of the immune system'),
(404852, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0101361', 'abnormal musculoabdominal vein', 0.4444444444444444, 5.809304221129108, 1.6068332169732154, 'UPHENO:0002678', 'abnormal vasculature'),
(404853, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0101221', 'abnormal larval immune system', 0.5, 5.64885357140806, 1.6806031017774632, 'HP:0002715', 'Abnormality of the immune system'),
(404854, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0100581', 'abnormal immune system', 0.52, 5.64885357140806, 1.713885602113569, 'HP:0002715', 'Abnormality of the immune system'),
(404855, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0127411', 'abnormally localised lymph vessel', 0.475, 8.696350005340756, 2.0324286586586156, 'HP:0100763', 'Abnormality of the lymphatic system'),
(404856, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0101170', 'abnormal arteria subclavia', 0.4444444444444444, 5.809304221129108, 1.6068332169732154, 'UPHENO:0002678', 'abnormal vasculature'),
(404857, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0100481', 'abnormal anatomical line', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(404858, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0126368', 'abnormally localised blood vessel', 0.43243243243243246, 5.809304221129108, 1.5849705218340364, 'UPHENO:0002678', 'abnormal vasculature'),
(404859, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0100449', 'abnormal lymphocyte', 0.4482758620689655, 5.64885357140806, 1.5913028324062968, 'HP:0002715', 'Abnormality of the immune system'),
(404860, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0107258', 'abnormal anatomical axis', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(404861, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0100599', 'abnormal adult immune system', 0.5, 5.64885357140806, 1.6806031017774632, 'HP:0002715', 'Abnormality of the immune system'),
(404862, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0101431', 'abnormal ischiadic artery', 0.5161290322580645, 5.809304221129108, 1.731574591446772, 'UPHENO:0002678', 'abnormal vasculature'),
(404863, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0100213', 'abnormal right channel of ventral aorta', 0.4444444444444444, 5.809304221129108, 1.6068332169732154, 'UPHENO:0002678', 'abnormal vasculature'),
(404864, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0100899', 'abnormal secondary spermatogonium', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(404865, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0141841', 'abnormality of whole organism mass', 0.41379310344827586, 2.13901709234296, 0.9408031255100615, 'UPHENO:0075696', 'abnormal anatomical entity'),
(404866, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0101435', 'abnormal paracrine cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(404867, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0100969', 'abnormal disaggregated/reaggregated ectoderm treated with activin', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(404868, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0100515', 'abnormal somatic stem cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(404869, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0100142', 'abnormal paired dorsal aorta', 0.5, 5.809304221129108, 1.7043039959363335, 'UPHENO:0002678', 'abnormal vasculature'),
(404870, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0126809', 'abnormally localised cardiovascular system', 0.4117647058823529, 5.249153838287537, 1.4701755971154233, 'UPHENO:0080362', 'abnormal cardiovascular system'),
(404871, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0101326', 'abnormal cementoblast', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(404872, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0100208', 'abnormal ventral aorta', 0.43243243243243246, 5.809304221129108, 1.5849705218340364, 'UPHENO:0002678', 'abnormal vasculature'),
(404873, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0100225', 'abnormal endocrine system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(404874, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0100791', 'abnormal multiciliated cell precursor', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(404875, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0100446', 'abnormal spleen', 0.4222222222222222, 8.696350005340756, 1.916192115753848, 'HP:0100763', 'Abnormality of the lymphatic system'),
(404876, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0102213', 'abnormal immune system morphology', 0.42424242424242425, 5.64885357140806, 1.548057923116778, 'HP:0002715', 'Abnormality of the immune system'),
(404877, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0126559', 'abnormally localised lymphatic system', 0.42424242424242425, 5.64885357140806, 1.548057923116778, 'HP:0002715', 'Abnormality of the immune system'),
(404878, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0101264', 'abnormal mitotic spindle', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(404879, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0131666', 'abnormal adherens junction', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(404880, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0100054', 'abnormal blood vessel', 0.5517241379310345, 5.809304221129108, 1.7902886257197683, 'UPHENO:0002678', 'abnormal vasculature'),
(404881, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0100674', 'abnormal secondary oogonium', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(404882, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0100533', 'abnormal melanoblast', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(404883, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0101535', 'abnormal absorptive cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(404884, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0126264', 'absent dorsal caudal lymphatic vessel', 0.4318181818181818, 8.696350005340756, 1.9378446913415897, 'HP:0100763', 'Abnormality of the lymphatic system'),
(404885, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0100308', 'abnormal early embryonic cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(404886, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0100652', 'abnormal medial cardinal vein', 0.4444444444444444, 5.809304221129108, 1.6068332169732154, 'UPHENO:0002678', 'abnormal vasculature'),
(404887, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0101257', 'abnormal coeliaco-mesenteric artery', 0.4444444444444444, 5.809304221129108, 1.6068332169732154, 'UPHENO:0002678', 'abnormal vasculature'),
(404888, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0100697', 'abnormal caudal artery', 0.4444444444444444, 5.809304221129108, 1.6068332169732154, 'UPHENO:0002678', 'abnormal vasculature'),
(404889, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0100902', 'abnormal spermatocyte', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(404890, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0100284', 'abnormal tail vasculature', 0.47058823529411764, 5.809304221129108, 1.6534177396253542, 'UPHENO:0002678', 'abnormal vasculature'),
(404891, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0100344', 'abnormal portion of organism substance', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(404892, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0142057', 'abnormal desmosome', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(404893, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0101071', 'abnormal endoplasmic reticulum', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(404894, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0100540', 'abnormal left lymph heart', 0.43333333333333335, 5.64885357140806, 1.5645563421015427, 'HP:0002715', 'Abnormality of the immune system'),
(404895, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0100534', 'abnormal medial abdominal vein', 0.4444444444444444, 5.809304221129108, 1.6068332169732154, 'UPHENO:0002678', 'abnormal vasculature'),
(404896, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0100317', 'abnormal respiratory system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
