(91282, 'HP:0003240', 'Increased phosphoribosylpyrophosphate synthetase level', 'XPO:0107258', 'abnormal anatomical axis', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91283, 'HP:0031592', 'Situs inversus with levocardia', 'XPO:0102113', 'abnormal anatomical line morphology', 0.4230769230769231, 2.6504988612427964, 1.0589451840551005, 'UPHENO:0076692', 'abnormal anatomical entity morphology'),
(91284, 'HP:0031592', 'Situs inversus with levocardia', 'XPO:0101638', 'abnormal anatomical structure morphology', 0.4230769230769231, 2.6504988612427964, 1.0589451840551005, 'UPHENO:0076692', 'abnormal anatomical entity morphology'),
(91285, 'HP:0031592', 'Situs inversus with levocardia', 'XPO:0101976', 'abnormal portion of organism substance morphology', 0.4230769230769231, 2.6504988612427964, 1.0589451840551005, 'UPHENO:0076692', 'abnormal anatomical entity morphology'),
(91286, 'HP:0031592', 'Situs inversus with levocardia', 'XPO:0101713', 'abnormal anatomical entity in vitro morphology', 0.4230769230769231, 2.6504988612427964, 1.0589451840551005, 'UPHENO:0076692', 'abnormal anatomical entity morphology'),
(91287, 'HP:0005327', 'Loss of facial expression', 'XPO:0100481', 'abnormal anatomical line', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(91288, 'HP:0005327', 'Loss of facial expression', 'XPO:0100344', 'abnormal portion of organism substance', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(91289, 'HP:0005327', 'Loss of facial expression', 'XPO:0100006', 'abnormal anatomical structure', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(91290, 'HP:0005327', 'Loss of facial expression', 'XPO:0100002', 'abnormal head', 0.4074074074074074, 3.869547816166077, 1.2555805205653743, 'UPHENO:0002844', 'abnormal head'),
(91291, 'HP:0005327', 'Loss of facial expression', 'XPO:0100081', 'abnormal anatomical entity in vitro', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(91292, 'HP:0005327', 'Loss of facial expression', 'XPO:0142052', 'abnormal nasal region', 0.4074074074074074, 3.869547816166077, 1.2555805205653743, 'UPHENO:0002844', 'abnormal head'),
(91293, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0141505', 'abnormal tadpole morphology', 0.42857142857142855, 3.008048030199787, 1.1354133350961642, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(91294, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0102739', 'abnormal erythroid cell morphology', 0.4117647058823529, 6.121988824155609, 1.5877087036334738, 'UPHENO:0084928', 'abnormal cell morphology'),
(91295, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0103005', 'abnormal oxygen accumulating cell morphology', 0.4827586206896552, 6.121988824155609, 1.7191401573539156, 'UPHENO:0084928', 'abnormal cell morphology'),
(91296, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0102549', 'abnormal stage III oocyte morphology', 0.42424242424242425, 6.121988824155609, 1.6115853622891974, 'UPHENO:0084928', 'abnormal cell morphology'),
(91297, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0141203', 'abnormally necrotic exocrine cell', 0.42424242424242425, 6.121988824155609, 1.6115853622891974, 'UPHENO:0084928', 'abnormal cell morphology'),
(91298, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0140269', 'abnormally necrotic anatomical line', 0.46153846153846156, 3.008048030199787, 1.178274102275107, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(91299, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0102773', 'abnormal Keller explant morphology', 0.46153846153846156, 3.008048030199787, 1.178274102275107, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(91300, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0140364', 'abnormally necrotic anterior region', 0.41379310344827586, 3.008048030199787, 1.1156655097912829, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(91301, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0139717', 'abnormally necrotic cell', 0.4666666666666667, 6.121988824155609, 1.6902449875504095, 'UPHENO:0084928', 'abnormal cell morphology'),
(91302, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0103202', 'abnormal forelimb region morphology', 0.42857142857142855, 3.008048030199787, 1.1354133350961642, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(91303, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0102768', 'abnormal ooplasm morphology', 0.40625, 4.8755453832354885, 1.4073699982376409, 'UPHENO:0086172', 'abnormal cell'),
(91304, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0101694', 'abnormal anatomical space morphology', 0.46153846153846156, 3.008048030199787, 1.178274102275107, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(91305, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0102353', 'abnormal centromere morphology', 0.43333333333333335, 4.8755453832354885, 1.453525484033692, 'UPHENO:0086172', 'abnormal cell'),
(91306, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0140955', 'abnormally necrotic ventro-lateral region', 0.41379310344827586, 3.008048030199787, 1.1156655097912829, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(91307, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0101976', 'abnormal portion of organism substance morphology', 0.5, 3.008048030199787, 1.2263865683787856, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(91308, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0140381', 'abnormally necrotic ciliated cell', 0.42424242424242425, 6.121988824155609, 1.6115853622891974, 'UPHENO:0084928', 'abnormal cell morphology'),
(91309, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0102147', 'abnormal somatic stem cell morphology', 0.45161290322580644, 6.121988824155609, 1.6627594974598268, 'UPHENO:0084928', 'abnormal cell morphology'),
(91310, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0141314', 'abnormal Roux spot morphology', 0.40625, 4.8755453832354885, 1.4073699982376409, 'UPHENO:0086172', 'abnormal cell'),
(91311, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0141299', 'abnormal actin filament morphology', 0.41935483870967744, 4.8755453832354885, 1.4298893480995063, 'UPHENO:0086172', 'abnormal cell'),
(91312, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0102764', 'abnormal apoptotic cell morphology', 0.4827586206896552, 6.121988824155609, 1.7191401573539156, 'UPHENO:0084928', 'abnormal cell morphology'),
(91313, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0107426', 'abnormal yolk platelet morphology', 0.40625, 4.8755453832354885, 1.4073699982376409, 'UPHENO:0086172', 'abnormal cell'),
(91314, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0102873', 'abnormal nucleate erythrocyte morphology', 0.4827586206896552, 6.121988824155609, 1.7191401573539156, 'UPHENO:0084928', 'abnormal cell morphology'),
(91315, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0141091', 'abnormally necrotic posterior region', 0.41379310344827586, 3.008048030199787, 1.1156655097912829, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(91316, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0102852', 'abnormal centriole morphology', 0.41935483870967744, 4.8755453832354885, 1.4298893480995063, 'UPHENO:0086172', 'abnormal cell'),
(91317, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0101927', 'abnormal extracellular matrix morphology', 0.41379310344827586, 3.008048030199787, 1.1156655097912829, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(91318, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0140709', 'abnormally necrotic acid secreting cell', 0.42424242424242425, 6.121988824155609, 1.6115853622891974, 'UPHENO:0084928', 'abnormal cell morphology'),
(91319, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0141254', 'abnormally necrotic dorso-lateral region', 0.41379310344827586, 3.008048030199787, 1.1156655097912829, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(91320, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0102531', 'abnormal secondary spermatogonium morphology', 0.45161290322580644, 6.121988824155609, 1.6627594974598268, 'UPHENO:0084928', 'abnormal cell morphology'),
(91321, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0103082', 'abnormal myeloid cell morphology', 0.4117647058823529, 6.121988824155609, 1.5877087036334738, 'UPHENO:0084928', 'abnormal cell morphology'),
(91322, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0141147', 'abnormally necrotic alkali secreting cell', 0.42424242424242425, 6.121988824155609, 1.6115853622891974, 'UPHENO:0084928', 'abnormal cell morphology'),
(91323, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0102636', 'abnormal acid secreting cell morphology', 0.4827586206896552, 6.121988824155609, 1.7191401573539156, 'UPHENO:0084928', 'abnormal cell morphology'),
(91324, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0107371', 'abnormal migrating myoblast morphology', 0.45161290322580644, 6.121988824155609, 1.6627594974598268, 'UPHENO:0084928', 'abnormal cell morphology'),
(91325, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0102024', 'abnormal cilium morphology', 0.41935483870967744, 4.8755453832354885, 1.4298893480995063, 'UPHENO:0086172', 'abnormal cell'),
(91326, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0102306', 'abnormal secondary oogonium morphology', 0.45161290322580644, 6.121988824155609, 1.6627594974598268, 'UPHENO:0084928', 'abnormal cell morphology'),
(91327, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0101828', 'abnormal neuron morphology', 0.4117647058823529, 6.121988824155609, 1.5877087036334738, 'UPHENO:0084928', 'abnormal cell morphology'),
(91328, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0101641', 'abnormal multi-tissue structure morphology', 0.41379310344827586, 3.008048030199787, 1.1156655097912829, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(91329, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0101657', 'abnormal oocyte morphology', 0.45161290322580644, 6.121988824155609, 1.6627594974598268, 'UPHENO:0084928', 'abnormal cell morphology'),
(91330, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0101740', 'abnormal cell part morphology', 0.4642857142857143, 4.8755453832354885, 1.5045418142371136, 'UPHENO:0086172', 'abnormal cell'),
(91331, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0140179', 'abnormally necrotic postero-dorsal region', 0.41379310344827586, 3.008048030199787, 1.1156655097912829, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(91332, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0102929', 'abnormal barrier cell morphology', 0.4827586206896552, 6.121988824155609, 1.7191401573539156, 'UPHENO:0084928', 'abnormal cell morphology'),
(91333, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0141316', 'abnormal anatomical region morphology', 0.46153846153846156, 3.008048030199787, 1.178274102275107, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(91334, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0101850', 'abnormal epithelial cell morphology', 0.4375, 6.121988824155609, 1.6365726719483247, 'UPHENO:0084928', 'abnormal cell morphology'),
(91335, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0140239', 'abnormally necrotic absorptive cell', 0.42424242424242425, 6.121988824155609, 1.6115853622891974, 'UPHENO:0084928', 'abnormal cell morphology'),
(91336, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0107357', 'abnormal proximal-distal axis morphology', 0.42857142857142855, 3.008048030199787, 1.1354133350961642, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(91337, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0103201', 'abnormal activin-induced ectoderm morphology', 0.46153846153846156, 3.008048030199787, 1.178274102275107, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(91338, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0101969', 'abnormal zygote morphology', 0.4827586206896552, 6.121988824155609, 1.7191401573539156, 'UPHENO:0084928', 'abnormal cell morphology'),
(91339, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0102356', 'abnormal kinetochore morphology', 0.43333333333333335, 4.8755453832354885, 1.453525484033692, 'UPHENO:0086172', 'abnormal cell'),
(91340, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0102534', 'abnormal spermatocyte morphology', 0.45161290322580644, 6.121988824155609, 1.6627594974598268, 'UPHENO:0084928', 'abnormal cell morphology'),
(91341, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0103099', 'abnormal alkali secreting cell morphology', 0.4827586206896552, 6.121988824155609, 1.7191401573539156, 'UPHENO:0084928', 'abnormal cell morphology'),
(91342, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0102532', 'abnormal angioblast morphology', 0.4117647058823529, 6.121988824155609, 1.5877087036334738, 'UPHENO:0084928', 'abnormal cell morphology'),
(91343, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0102183', 'abnormal oocyte cortex morphology', 0.40625, 4.8755453832354885, 1.4073699982376409, 'UPHENO:0086172', 'abnormal cell'),
(91344, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0101702', 'abnormal anatomical system morphology', 0.41379310344827586, 3.008048030199787, 1.1156655097912829, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(91345, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0101807', 'abnormal migrating neuroblast morphology', 0.4117647058823529, 6.121988824155609, 1.5877087036334738, 'UPHENO:0084928', 'abnormal cell morphology'),
(91346, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0107346', 'abnormal animal-vegetal axis morphology', 0.42857142857142855, 3.008048030199787, 1.1354133350961642, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(91347, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0141048', 'abnormally necrotic mitotic cell', 0.42424242424242425, 6.121988824155609, 1.6115853622891974, 'UPHENO:0084928', 'abnormal cell morphology'),
(91348, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0101835', 'abnormal endocrine cell morphology', 0.4117647058823529, 6.121988824155609, 1.5877087036334738, 'UPHENO:0084928', 'abnormal cell morphology'),
(91349, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0102958', 'abnormal cementoblast morphology', 0.4827586206896552, 6.121988824155609, 1.7191401573539156, 'UPHENO:0084928', 'abnormal cell morphology'),
(91350, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0102055', 'abnormal process morphology', 0.4444444444444444, 3.008048030199787, 1.1562483451423184, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(91351, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0101635', 'abnormal organism subdivision morphology', 0.41379310344827586, 3.008048030199787, 1.1156655097912829, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(91352, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0102896', 'abnormal mitotic spindle morphology', 0.43333333333333335, 4.8755453832354885, 1.453525484033692, 'UPHENO:0086172', 'abnormal cell'),
(91353, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0141277', 'abnormal actin cytoskeleton morphology', 0.43333333333333335, 4.8755453832354885, 1.453525484033692, 'UPHENO:0086172', 'abnormal cell'),
(91354, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0140075', 'abnormally necrotic stem cell', 0.42424242424242425, 6.121988824155609, 1.6115853622891974, 'UPHENO:0084928', 'abnormal cell morphology'),
(91355, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0102270', 'abnormal polar body morphology', 0.4375, 6.121988824155609, 1.6365726719483247, 'UPHENO:0084928', 'abnormal cell morphology'),
(91356, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0141285', 'abnormal cortical actin cytoskeleton morphology', 0.41935483870967744, 4.8755453832354885, 1.4298893480995063, 'UPHENO:0086172', 'abnormal cell'),
(91357, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0102741', 'abnormal egg cell-free extract morphology', 0.42857142857142855, 3.008048030199787, 1.1354133350961642, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(91358, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0102539', 'abnormal cytoplasm morphology', 0.43333333333333335, 4.8755453832354885, 1.453525484033692, 'UPHENO:0086172', 'abnormal cell'),
(91359, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0139841', 'abnormally necrotic anatomical region', 0.42857142857142855, 3.008048030199787, 1.1354133350961642, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(91360, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0102601', 'abnormal disaggregated/reaggregated ectoderm treated with activin morphology', 0.46153846153846156, 3.008048030199787, 1.178274102275107, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(91361, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0103927', 'decreased pigmentation in the whole organism', 0.41379310344827586, 3.008048030199787, 1.1156655097912829, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(91362, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0102206', 'abnormal gastrula cell morphology', 0.42424242424242425, 6.121988824155609, 1.6115853622891974, 'UPHENO:0084928', 'abnormal cell morphology'),
(91363, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0102704', 'abnormal mitochondrial cloud morphology', 0.40625, 4.8755453832354885, 1.4073699982376409, 'UPHENO:0086172', 'abnormal cell'),
(91364, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0102061', 'abnormal spermatid morphology', 0.45161290322580644, 6.121988824155609, 1.6627594974598268, 'UPHENO:0084928', 'abnormal cell morphology'),
(91365, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0101642', 'abnormal multicellular anatomical structure morphology', 0.4444444444444444, 3.008048030199787, 1.1562483451423184, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(91366, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0103021', 'abnormal wedge region morphology', 0.40625, 4.8755453832354885, 1.4073699982376409, 'UPHENO:0086172', 'abnormal cell'),
(91367, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0100081', 'abnormal anatomical entity in vitro', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(91368, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0140899', 'abnormally necrotic mucus secreting cell', 0.42424242424242425, 6.121988824155609, 1.6115853622891974, 'UPHENO:0084928', 'abnormal cell morphology'),
(91369, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0101660', 'abnormal anatomical cluster morphology', 0.41379310344827586, 3.008048030199787, 1.1156655097912829, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(91370, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0103145', 'abnormal basal body morphology', 0.43333333333333335, 4.8755453832354885, 1.453525484033692, 'UPHENO:0086172', 'abnormal cell'),
(91371, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0129487', 'increased size of the anatomical structure', 0.42857142857142855, 3.008048030199787, 1.1354133350961642, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(91372, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0102336', 'abnormal Merkel cell morphology', 0.4827586206896552, 6.121988824155609, 1.7191401573539156, 'UPHENO:0084928', 'abnormal cell morphology'),
(91373, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0102789', 'abnormal female organism morphology', 0.42857142857142855, 3.008048030199787, 1.1354133350961642, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(91374, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0101808', 'abnormal stage VI oocyte morphology', 0.42424242424242425, 6.121988824155609, 1.6115853622891974, 'UPHENO:0084928', 'abnormal cell morphology'),
(91375, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0101834', 'abnormal embryo morphology', 0.41379310344827586, 3.008048030199787, 1.1156655097912829, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(91376, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0141334', 'increased pigmentation in the whole organism', 0.41379310344827586, 3.008048030199787, 1.1156655097912829, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(91377, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0102334', 'abnormal glial cell morphology', 0.4117647058823529, 6.121988824155609, 1.5877087036334738, 'UPHENO:0084928', 'abnormal cell morphology'),
(91378, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0102275', 'abnormal thoracic region morphology', 0.42857142857142855, 3.008048030199787, 1.1354133350961642, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(91379, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0141503', 'abnormal lymphoblast morphology', 0.4117647058823529, 6.121988824155609, 1.5877087036334738, 'UPHENO:0084928', 'abnormal cell morphology'),
(91380, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0140919', 'abnormally necrotic cementoblast', 0.42424242424242425, 6.121988824155609, 1.6115853622891974, 'UPHENO:0084928', 'abnormal cell morphology'),
(91381, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0100006', 'abnormal anatomical structure', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(91382, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0102860', 'abnormal mesenchymal stem cell morphology', 0.45161290322580644, 6.121988824155609, 1.6627594974598268, 'UPHENO:0084928', 'abnormal cell morphology'),
(91383, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0140052', 'abnormally necrotic organ part', 0.41379310344827586, 3.008048030199787, 1.1156655097912829, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(91384, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0101897', 'abnormal sensory epithelial cell morphology', 0.4117647058823529, 6.121988824155609, 1.5877087036334738, 'UPHENO:0084928', 'abnormal cell morphology'),
(91385, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0140068', 'abnormally necrotic myoblast', 0.42424242424242425, 6.121988824155609, 1.6115853622891974, 'UPHENO:0084928', 'abnormal cell morphology'),
(91386, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0140752', 'abnormally necrotic melanoblast', 0.42424242424242425, 6.121988824155609, 1.6115853622891974, 'UPHENO:0084928', 'abnormal cell morphology'),
(91387, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0107350', 'abnormal anatomical side morphology', 0.42857142857142855, 3.008048030199787, 1.1354133350961642, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(91388, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0102109', 'abnormal pericyte morphology', 0.4827586206896552, 6.121988824155609, 1.7191401573539156, 'UPHENO:0084928', 'abnormal cell morphology'),
(91389, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0139839', 'abnormally necrotic progenitor cell', 0.42424242424242425, 6.121988824155609, 1.6115853622891974, 'UPHENO:0084928', 'abnormal cell morphology'),
(91390, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0102258', 'abnormal primordial germ cell morphology', 0.45161290322580644, 6.121988824155609, 1.6627594974598268, 'UPHENO:0084928', 'abnormal cell morphology'),
(91391, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0102434', 'abnormal exocrine cell morphology', 0.4827586206896552, 6.121988824155609, 1.7191401573539156, 'UPHENO:0084928', 'abnormal cell morphology'),
(91392, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0103130', 'abnormal stage II oocyte morphology', 0.42424242424242425, 6.121988824155609, 1.6115853622891974, 'UPHENO:0084928', 'abnormal cell morphology'),
(91393, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0128102', 'decreased size of the portion of organism substance', 0.42857142857142855, 3.008048030199787, 1.1354133350961642, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(91394, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0101736', 'abnormal embryonic structure morphology', 0.41379310344827586, 3.008048030199787, 1.1156655097912829, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(91395, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0102588', 'abnormal centrosome morphology', 0.43333333333333335, 4.8755453832354885, 1.453525484033692, 'UPHENO:0086172', 'abnormal cell'),
(91396, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0107345', 'abnormal anatomical axis morphology', 0.46153846153846156, 3.008048030199787, 1.178274102275107, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(91397, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0141165', 'abnormally necrotic ventral region', 0.41379310344827586, 3.008048030199787, 1.1156655097912829, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(91398, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0100481', 'abnormal anatomical line', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(91399, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0141007', 'abnormally necrotic electrically active cell', 0.42424242424242425, 6.121988824155609, 1.6115853622891974, 'UPHENO:0084928', 'abnormal cell morphology'),
(91400, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0103179', 'abnormal lampbrush chromosome morphology', 0.43333333333333335, 4.8755453832354885, 1.453525484033692, 'UPHENO:0086172', 'abnormal cell'),
(91401, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0103219', 'abnormal hemangioblast morphology', 0.4117647058823529, 6.121988824155609, 1.5877087036334738, 'UPHENO:0084928', 'abnormal cell morphology'),
(91402, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0102526', 'abnormal nucleus morphology', 0.43333333333333335, 4.8755453832354885, 1.453525484033692, 'UPHENO:0086172', 'abnormal cell'),
(91403, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0140395', 'abnormally necrotic antero-dorsal region', 0.41379310344827586, 3.008048030199787, 1.1156655097912829, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(91404, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0102205', 'abnormal extraembryonic structure morphology', 0.42857142857142855, 3.008048030199787, 1.1354133350961642, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(91405, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0107349', 'abnormal left-right axis morphology', 0.42857142857142855, 3.008048030199787, 1.1354133350961642, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(91406, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0102047', 'abnormal secretory epithelial cell morphology', 0.4117647058823529, 6.121988824155609, 1.5877087036334738, 'UPHENO:0084928', 'abnormal cell morphology'),
(91407, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0107348', 'abnormal dorsal-ventral axis morphology', 0.42857142857142855, 3.008048030199787, 1.1354133350961642, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(91408, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0102693', 'abnormal plasma membrane morphology', 0.43333333333333335, 4.8755453832354885, 1.453525484033692, 'UPHENO:0086172', 'abnormal cell'),
(91409, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0101646', 'abnormal tissue morphology', 0.41379310344827586, 3.008048030199787, 1.1156655097912829, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(91410, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0141154', 'abnormally necrotic barrier cell', 0.42424242424242425, 6.121988824155609, 1.6115853622891974, 'UPHENO:0084928', 'abnormal cell morphology'),
(91411, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0102998', 'abnormal morula cell morphology', 0.42424242424242425, 6.121988824155609, 1.6115853622891974, 'UPHENO:0084928', 'abnormal cell morphology'),
(91412, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0102608', 'abnormal multiciliated cell morphology', 0.45161290322580644, 6.121988824155609, 1.6627594974598268, 'UPHENO:0084928', 'abnormal cell morphology'),
(91413, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0102800', 'abnormal circulating cell morphology', 0.4117647058823529, 6.121988824155609, 1.5877087036334738, 'UPHENO:0084928', 'abnormal cell morphology'),
(91414, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0139929', 'abnormally necrotic barrier epithelial cell', 0.42424242424242425, 6.121988824155609, 1.6115853622891974, 'UPHENO:0084928', 'abnormal cell morphology'),
(91415, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0103112', 'abnormal stage V oocyte morphology', 0.42424242424242425, 6.121988824155609, 1.6115853622891974, 'UPHENO:0084928', 'abnormal cell morphology'),
(91416, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0128502', 'decreased size of the anatomical line', 0.42857142857142855, 3.008048030199787, 1.1354133350961642, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(91417, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0141065', 'abnormally necrotic paracrine cell', 0.42424242424242425, 6.121988824155609, 1.6115853622891974, 'UPHENO:0084928', 'abnormal cell morphology'),
(91418, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0129982', 'increased size of the anatomical line', 0.42857142857142855, 3.008048030199787, 1.1354133350961642, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(91419, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0115510', 'abnormal degeneration of whole organism', 0.4444444444444444, 3.008048030199787, 1.1562483451423184, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(91420, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0102872', 'abnormal ciliated non-epidermal cell morphology', 0.45161290322580644, 6.121988824155609, 1.6627594974598268, 'UPHENO:0084928', 'abnormal cell morphology'),
(91421, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0102979', 'abnormal hindlimb region morphology', 0.42857142857142855, 3.008048030199787, 1.1354133350961642, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(91422, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0140803', 'abnormally necrotic pericyte', 0.42424242424242425, 6.121988824155609, 1.6115853622891974, 'UPHENO:0084928', 'abnormal cell morphology'),
(91423, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0100004', 'abnormal cell', 0.4166666666666667, 4.8755453832354885, 1.4252990012677296, 'UPHENO:0086172', 'abnormal cell'),
(91424, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0101658', 'abnormal germ cell morphology', 0.4827586206896552, 6.121988824155609, 1.7191401573539156, 'UPHENO:0084928', 'abnormal cell morphology'),
(91425, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0103043', 'abnormal marginal zone (sensu neural) morphology', 0.42857142857142855, 3.008048030199787, 1.1354133350961642, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(91426, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0141189', 'abnormally necrotic antero-ventral region', 0.41379310344827586, 3.008048030199787, 1.1156655097912829, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(91427, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0102297', 'abnormal egg jelly morphology', 0.41379310344827586, 3.008048030199787, 1.1156655097912829, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(91428, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0140373', 'abnormally necrotic whole organism', 0.41379310344827586, 3.008048030199787, 1.1156655097912829, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(91429, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0140589', 'abnormally necrotic keratin accumulating cell', 0.42424242424242425, 6.121988824155609, 1.6115853622891974, 'UPHENO:0084928', 'abnormal cell morphology'),
(91430, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0107399', 'abnormal filopodium morphology', 0.43333333333333335, 4.8755453832354885, 1.453525484033692, 'UPHENO:0086172', 'abnormal cell'),
(91431, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0141289', 'abnormal spindle microtubule morphology', 0.40625, 4.8755453832354885, 1.4073699982376409, 'UPHENO:0086172', 'abnormal cell'),
(91432, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0102360', 'abnormal cell condensation morphology', 0.4444444444444444, 3.008048030199787, 1.1562483451423184, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(91433, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0128007', 'decreased size of the anatomical structure', 0.42857142857142855, 3.008048030199787, 1.1354133350961642, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(91434, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0102808', 'abnormal non-ciliated epithelial cell morphology', 0.4117647058823529, 6.121988824155609, 1.5877087036334738, 'UPHENO:0084928', 'abnormal cell morphology'),
(91435, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0101713', 'abnormal anatomical entity in vitro morphology', 0.5, 3.008048030199787, 1.2263865683787856, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(91436, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0101939', 'abnormal blastomere morphology', 0.42424242424242425, 6.121988824155609, 1.6115853622891974, 'UPHENO:0084928', 'abnormal cell morphology'),
(91437, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0102742', 'abnormal cell-free extract morphology', 0.46153846153846156, 3.008048030199787, 1.178274102275107, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(91438, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0103080', 'abnormal myelin accumulating cell morphology', 0.4827586206896552, 6.121988824155609, 1.7191401573539156, 'UPHENO:0084928', 'abnormal cell morphology'),
(91439, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0102285', 'abnormal myoblast morphology', 0.4827586206896552, 6.121988824155609, 1.7191401573539156, 'UPHENO:0084928', 'abnormal cell morphology'),
(91440, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0140533', 'abnormally necrotic myelin accumulating cell', 0.42424242424242425, 6.121988824155609, 1.6115853622891974, 'UPHENO:0084928', 'abnormal cell morphology'),
(91441, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0107347', 'abnormal anterior-posterior axis morphology', 0.42857142857142855, 3.008048030199787, 1.1354133350961642, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(91442, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0103037', 'abnormal ring structure morphology', 0.40625, 4.8755453832354885, 1.4073699982376409, 'UPHENO:0086172', 'abnormal cell'),
(91443, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0129582', 'increased size of the portion of organism substance', 0.42857142857142855, 3.008048030199787, 1.1354133350961642, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(91444, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0102178', 'abnormal whole organism morphology', 0.46153846153846156, 3.008048030199787, 1.178274102275107, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(91445, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0139718', 'abnormally necrotic anatomical structure', 0.46153846153846156, 3.008048030199787, 1.178274102275107, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(91446, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0102703', 'abnormal endoplasmic reticulum morphology', 0.43333333333333335, 4.8755453832354885, 1.453525484033692, 'UPHENO:0086172', 'abnormal cell'),
(91447, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0103104', 'abnormal zygote cortex morphology', 0.41935483870967744, 4.8755453832354885, 1.4298893480995063, 'UPHENO:0086172', 'abnormal cell'),
(91448, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0102965', 'abnormal barrier epithelial cell morphology', 0.4827586206896552, 6.121988824155609, 1.7191401573539156, 'UPHENO:0084928', 'abnormal cell morphology'),
(91449, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0140868', 'abnormally necrotic chondroblast', 0.42424242424242425, 6.121988824155609, 1.6115853622891974, 'UPHENO:0084928', 'abnormal cell morphology'),
(91450, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0102423', 'abnormal multiciliated cell precursor morphology', 0.4827586206896552, 6.121988824155609, 1.7191401573539156, 'UPHENO:0084928', 'abnormal cell morphology'),
(91451, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0101871', 'abnormal acellular anatomical structure morphology', 0.4444444444444444, 3.008048030199787, 1.1562483451423184, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(91452, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0102323', 'abnormal keratin accumulating cell morphology', 0.4827586206896552, 6.121988824155609, 1.7191401573539156, 'UPHENO:0084928', 'abnormal cell morphology'),
(91453, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0102386', 'abnormal electrically active cell morphology', 0.4827586206896552, 6.121988824155609, 1.7191401573539156, 'UPHENO:0084928', 'abnormal cell morphology'),
(91454, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0140567', 'abnormally necrotic postero-ventral region', 0.41379310344827586, 3.008048030199787, 1.1156655097912829, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(91455, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0140144', 'abnormally necrotic portion of organism substance', 0.46153846153846156, 3.008048030199787, 1.178274102275107, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(91456, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0102181', 'abnormal mitotic cell morphology', 0.4827586206896552, 6.121988824155609, 1.7191401573539156, 'UPHENO:0084928', 'abnormal cell morphology'),
(91457, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0102745', 'abnormal stage IV oocyte morphology', 0.42424242424242425, 6.121988824155609, 1.6115853622891974, 'UPHENO:0084928', 'abnormal cell morphology'),
(91458, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0101917', 'abnormal progenitor cell morphology', 0.4827586206896552, 6.121988824155609, 1.7191401573539156, 'UPHENO:0084928', 'abnormal cell morphology'),
(91459, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0102177', 'abnormal male organism morphology', 0.42857142857142855, 3.008048030199787, 1.1354133350961642, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(91460, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0102934', 'abnormal subcortical cytoplasm morphology', 0.40625, 4.8755453832354885, 1.4073699982376409, 'UPHENO:0086172', 'abnormal cell'),
(91461, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0102081', 'abnormal lymphocyte morphology', 0.4117647058823529, 6.121988824155609, 1.5877087036334738, 'UPHENO:0084928', 'abnormal cell morphology'),
(91462, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0103067', 'abnormal paracrine cell morphology', 0.4827586206896552, 6.121988824155609, 1.7191401573539156, 'UPHENO:0084928', 'abnormal cell morphology'),
(91463, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0102113', 'abnormal anatomical line morphology', 0.5, 3.008048030199787, 1.2263865683787856, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(91464, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0101636', 'abnormal cell morphology', 0.5185185185185185, 6.121988824155609, 1.7816746547807467, 'UPHENO:0084928', 'abnormal cell morphology'),
(91465, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0102520', 'abnormal microtubule morphology', 0.43333333333333335, 4.8755453832354885, 1.453525484033692, 'UPHENO:0086172', 'abnormal cell'),
(91466, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0102869', 'abnormal mucus secreting cell morphology', 0.4827586206896552, 6.121988824155609, 1.7191401573539156, 'UPHENO:0084928', 'abnormal cell morphology'),
(91467, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0107359', 'abnormal axial region morphology', 0.42857142857142855, 3.008048030199787, 1.1354133350961642, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(91468, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0140647', 'abnormally necrotic nucleate erythrocyte', 0.42424242424242425, 6.121988824155609, 1.6115853622891974, 'UPHENO:0084928', 'abnormal cell morphology'),
(91469, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0102347', 'abnormal ciliated cell morphology', 0.4827586206896552, 6.121988824155609, 1.7191401573539156, 'UPHENO:0084928', 'abnormal cell morphology'),
(91470, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0103167', 'abnormal absorptive cell morphology', 0.4827586206896552, 6.121988824155609, 1.7191401573539156, 'UPHENO:0084928', 'abnormal cell morphology'),
(91471, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0101804', 'abnormal stem cell morphology', 0.4827586206896552, 6.121988824155609, 1.7191401573539156, 'UPHENO:0084928', 'abnormal cell morphology'),
(91472, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0102794', 'abnormal stromal cell morphology', 0.42424242424242425, 6.121988824155609, 1.6115853622891974, 'UPHENO:0084928', 'abnormal cell morphology'),
(91473, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0101909', 'abnormal blastocoel morphology', 0.41379310344827586, 3.008048030199787, 1.1156655097912829, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(91474, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0101921', 'abnormal chondroblast morphology', 0.4827586206896552, 6.121988824155609, 1.7191401573539156, 'UPHENO:0084928', 'abnormal cell morphology'),
(91475, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0100344', 'abnormal portion of organism substance', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(91476, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0103041', 'abnormal perivitelline space morphology', 0.40625, 4.8755453832354885, 1.4073699982376409, 'UPHENO:0086172', 'abnormal cell'),
(91477, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0102165', 'abnormal melanoblast morphology', 0.4827586206896552, 6.121988824155609, 1.7191401573539156, 'UPHENO:0084928', 'abnormal cell morphology'),
(91478, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0140600', 'abnormally necrotic apoptotic cell', 0.42424242424242425, 6.121988824155609, 1.6115853622891974, 'UPHENO:0084928', 'abnormal cell morphology'),
(91479, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0139759', 'abnormally necrotic germ cell', 0.42424242424242425, 6.121988824155609, 1.6115853622891974, 'UPHENO:0084928', 'abnormal cell morphology'),
(91480, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0101940', 'abnormal early embryonic cell morphology', 0.45161290322580644, 6.121988824155609, 1.6627594974598268, 'UPHENO:0084928', 'abnormal cell morphology'),
(91481, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0103093', 'abnormal sperm entry point morphology', 0.41935483870967744, 4.8755453832354885, 1.4298893480995063, 'UPHENO:0086172', 'abnormal cell'),
(91482, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0141146', 'abnormally necrotic oxygen accumulating cell', 0.42424242424242425, 6.121988824155609, 1.6115853622891974, 'UPHENO:0084928', 'abnormal cell morphology'),
(91483, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0103129', 'abnormal ciliary axoneme morphology', 0.40625, 4.8755453832354885, 1.4073699982376409, 'UPHENO:0086172', 'abnormal cell'),
(91484, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0102069', 'abnormal proepicardium morphology', 0.45161290322580644, 6.121988824155609, 1.6627594974598268, 'UPHENO:0084928', 'abnormal cell morphology'),
(91485, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0140010', 'abnormally necrotic zygote', 0.42424242424242425, 6.121988824155609, 1.6115853622891974, 'UPHENO:0084928', 'abnormal cell morphology'),
(91486, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0101638', 'abnormal anatomical structure morphology', 0.5, 3.008048030199787, 1.2263865683787856, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(91487, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0103100', 'abnormal stage I oocyte morphology', 0.42424242424242425, 6.121988824155609, 1.6115853622891974, 'UPHENO:0084928', 'abnormal cell morphology'),
(91488, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0142064', 'abnormal desmosome morphology', 0.43333333333333335, 4.8755453832354885, 1.453525484033692, 'UPHENO:0086172', 'abnormal cell'),
(91489, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0101716', 'abnormal anatomical group morphology', 0.4444444444444444, 3.008048030199787, 1.1562483451423184, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(91490, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0141296', 'abnormal adherens junction morphology', 0.43333333333333335, 4.8755453832354885, 1.453525484033692, 'UPHENO:0086172', 'abnormal cell'),
(91491, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0140278', 'abnormally necrotic Merkel cell', 0.42424242424242425, 6.121988824155609, 1.6115853622891974, 'UPHENO:0084928', 'abnormal cell morphology'),
(91492, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0102832', 'abnormal joint region morphology', 0.42857142857142855, 3.008048030199787, 1.1354133350961642, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(91493, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0101890', 'abnormal organ part morphology', 0.46153846153846156, 3.008048030199787, 1.178274102275107, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(91494, 'HP:0020156', 'Abnormal zona pellucida morphology', 'XPO:0140471', 'abnormally necrotic multiciliated cell precursor', 0.42424242424242425, 6.121988824155609, 1.6115853622891974, 'UPHENO:0084928', 'abnormal cell morphology'),
(91495, 'HP:0012103', 'Abnormality of the mitochondrion', 'XPO:0107259', 'abnormal animal-vegetal axis', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(91496, 'HP:0012103', 'Abnormality of the mitochondrion', 'XPO:0100674', 'abnormal secondary oogonium', 0.4166666666666667, 4.8755453832354885, 1.4252990012677296, 'UPHENO:0086172', 'abnormal cell'),
(91497, 'HP:0012103', 'Abnormality of the mitochondrion', 'XPO:0100969', 'abnormal disaggregated/reaggregated ectoderm treated with activin', 0.42857142857142855, 1.7901636446558942, 0.8759069531444602, 'UPHENO:0002536', 'abnormal anatomical entity'),
(91498, 'HP:0012103', 'Abnormality of the mitochondrion', 'XPO:0142057', 'abnormal desmosome', 0.4166666666666667, 4.8755453832354885, 1.4252990012677296, 'UPHENO:0086172', 'abnormal cell'),
(91499, 'HP:0012103', 'Abnormality of the mitochondrion', 'XPO:0100344', 'abnormal portion of organism substance', 0.45, 1.7901636446558942, 0.8975375424432965, 'UPHENO:0002536', 'abnormal anatomical entity'),
(91500, 'HP:0012103', 'Abnormality of the mitochondrion', 'XPO:0100653', 'abnormal myoblast', 0.43478260869565216, 4.8755453832354885, 1.4559540997356917, 'UPHENO:0086172', 'abnormal cell'),
(91501, 'HP:0012103', 'Abnormality of the mitochondrion', 'XPO:0115512', 'abnormally semi-erect whole organism', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(91502, 'HP:0012103', 'Abnormality of the mitochondrion', 'XPO:0101264', 'abnormal mitotic spindle', 0.4166666666666667, 4.8755453832354885, 1.4252990012677296, 'UPHENO:0086172', 'abnormal cell'),
(91503, 'HP:0012103', 'Abnormality of the mitochondrion', 'XPO:0100108', 'abnormal cell part', 0.43478260869565216, 4.8755453832354885, 1.4559540997356917, 'UPHENO:0086172', 'abnormal cell'),
(91504, 'HP:0012103', 'Abnormality of the mitochondrion', 'XPO:0107284', 'abnormal migrating myoblast', 0.4166666666666667, 4.8755453832354885, 1.4252990012677296, 'UPHENO:0086172', 'abnormal cell'),
(91505, 'HP:0012103', 'Abnormality of the mitochondrion', 'XPO:0100899', 'abnormal secondary spermatogonium', 0.4166666666666667, 4.8755453832354885, 1.4252990012677296, 'UPHENO:0086172', 'abnormal cell'),
(91506, 'HP:0012103', 'Abnormality of the mitochondrion', 'XPO:0101132', 'abnormal apoptotic cell', 0.43478260869565216, 4.8755453832354885, 1.4559540997356917, 'UPHENO:0086172', 'abnormal cell'),
(91507, 'HP:0012103', 'Abnormality of the mitochondrion', 'XPO:0100802', 'abnormal exocrine cell', 0.43478260869565216, 4.8755453832354885, 1.4559540997356917, 'UPHENO:0086172', 'abnormal cell'),
(91508, 'HP:0012103', 'Abnormality of the mitochondrion', 'XPO:0101237', 'abnormal mucus secreting cell', 0.43478260869565216, 4.8755453832354885, 1.4559540997356917, 'UPHENO:0086172', 'abnormal cell'),
(91509, 'HP:0012103', 'Abnormality of the mitochondrion', 'XPO:0131666', 'abnormal adherens junction', 0.4166666666666667, 4.8755453832354885, 1.4252990012677296, 'UPHENO:0086172', 'abnormal cell'),
(91510, 'HP:0012103', 'Abnormality of the mitochondrion', 'XPO:0100728', 'abnormal cell condensation', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(91511, 'HP:0012103', 'Abnormality of the mitochondrion', 'XPO:0100062', 'abnormal anatomical space', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(91512, 'HP:0012103', 'Abnormality of the mitochondrion', 'XPO:0100956', 'abnormal centrosome', 0.4166666666666667, 4.8755453832354885, 1.4252990012677296, 'UPHENO:0086172', 'abnormal cell'),
(91513, 'HP:0012103', 'Abnormality of the mitochondrion', 'XPO:0100239', 'abnormal acellular anatomical structure', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(91514, 'HP:0012103', 'Abnormality of the mitochondrion', 'XPO:0107261', 'abnormal dorsal-ventral axis', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(91515, 'HP:0012103', 'Abnormality of the mitochondrion', 'XPO:0101004', 'abnormal acid secreting cell', 0.43478260869565216, 4.8755453832354885, 1.4559540997356917, 'UPHENO:0086172', 'abnormal cell'),
(91516, 'HP:0012103', 'Abnormality of the mitochondrion', 'XPO:0100172', 'abnormal stem cell', 0.43478260869565216, 4.8755453832354885, 1.4559540997356917, 'UPHENO:0086172', 'abnormal cell'),
(91517, 'HP:0012103', 'Abnormality of the mitochondrion', 'XPO:0100515', 'abnormal somatic stem cell', 0.4166666666666667, 4.8755453832354885, 1.4252990012677296, 'UPHENO:0086172', 'abnormal cell'),
(91518, 'HP:0012103', 'Abnormality of the mitochondrion', 'XPO:0100437', 'abnormal proepicardium', 0.4166666666666667, 4.8755453832354885, 1.4252990012677296, 'UPHENO:0086172', 'abnormal cell'),
(91519, 'HP:0012103', 'Abnormality of the mitochondrion', 'XPO:0115508', 'abnormally peramorphic growth of whole organism', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(91520, 'HP:0012103', 'Abnormality of the mitochondrion', 'XPO:0100715', 'abnormal ciliated cell', 0.43478260869565216, 4.8755453832354885, 1.4559540997356917, 'UPHENO:0086172', 'abnormal cell'),
(91521, 'HP:0012103', 'Abnormality of the mitochondrion', 'XPO:0100691', 'abnormal keratin accumulating cell', 0.43478260869565216, 4.8755453832354885, 1.4559540997356917, 'UPHENO:0086172', 'abnormal cell'),
(91522, 'HP:0012103', 'Abnormality of the mitochondrion', 'XPO:0100025', 'abnormal oocyte', 0.4166666666666667, 4.8755453832354885, 1.4252990012677296, 'UPHENO:0086172', 'abnormal cell'),
(91523, 'HP:0012103', 'Abnormality of the mitochondrion', 'XPO:0100429', 'abnormal spermatid', 0.4166666666666667, 4.8755453832354885, 1.4252990012677296, 'UPHENO:0086172', 'abnormal cell'),
(91524, 'HP:0012103', 'Abnormality of the mitochondrion', 'XPO:0100081', 'abnormal anatomical entity in vitro', 0.45, 1.7901636446558942, 0.8975375424432965, 'UPHENO:0002536', 'abnormal anatomical entity'),
(91525, 'HP:0012103', 'Abnormality of the mitochondrion', 'XPO:0100004', 'abnormal cell', 0.45454545454545453, 4.8755453832354885, 1.4886762550601012, 'UPHENO:0086172', 'abnormal cell'),
(91526, 'HP:0012103', 'Abnormality of the mitochondrion', 'XPO:0101569', 'abnormal activin-induced ectoderm', 0.42857142857142855, 1.7901636446558942, 0.8759069531444602, 'UPHENO:0002536', 'abnormal anatomical entity'),
(91527, 'HP:0012103', 'Abnormality of the mitochondrion', 'XPO:0141315', 'abnormal anatomical region', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(91528, 'HP:0012103', 'Abnormality of the mitochondrion', 'XPO:0101109', 'abnormal egg cell-free extract', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(91529, 'HP:0012103', 'Abnormality of the mitochondrion', 'XPO:0100549', 'abnormal mitotic cell', 0.43478260869565216, 4.8755453832354885, 1.4559540997356917, 'UPHENO:0086172', 'abnormal cell'),
(91530, 'HP:0012103', 'Abnormality of the mitochondrion', 'XPO:0107312', 'abnormal filopodium', 0.4166666666666667, 4.8755453832354885, 1.4252990012677296, 'UPHENO:0086172', 'abnormal cell'),
(91531, 'HP:0012103', 'Abnormality of the mitochondrion', 'XPO:0100638', 'abnormal polar body', 0.43478260869565216, 4.8755453832354885, 1.4559540997356917, 'UPHENO:0086172', 'abnormal cell'),
(91532, 'HP:0012103', 'Abnormality of the mitochondrion', 'XPO:0107262', 'abnormal left-right axis', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(91533, 'HP:0012103', 'Abnormality of the mitochondrion', 'XPO:0101240', 'abnormal ciliated non-epidermal cell', 0.4166666666666667, 4.8755453832354885, 1.4252990012677296, 'UPHENO:0086172', 'abnormal cell'),
(91534, 'HP:0012103', 'Abnormality of the mitochondrion', 'XPO:0100202', 'abnormal embryo', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(91535, 'HP:0012103', 'Abnormality of the mitochondrion', 'XPO:0100907', 'abnormal cytoplasm', 0.4166666666666667, 4.8755453832354885, 1.4252990012677296, 'UPHENO:0086172', 'abnormal cell'),
(91536, 'HP:0012103', 'Abnormality of the mitochondrion', 'XPO:0101373', 'abnormal oxygen accumulating cell', 0.43478260869565216, 4.8755453832354885, 1.4559540997356917, 'UPHENO:0086172', 'abnormal cell'),
(91537, 'HP:0012103', 'Abnormality of the mitochondrion', 'XPO:0101061', 'abnormal plasma membrane', 0.4166666666666667, 4.8755453832354885, 1.4252990012677296, 'UPHENO:0086172', 'abnormal cell'),
(91538, 'HP:0012103', 'Abnormality of the mitochondrion', 'XPO:0101448', 'abnormal myelin accumulating cell', 0.43478260869565216, 4.8755453832354885, 1.4559540997356917, 'UPHENO:0086172', 'abnormal cell'),
(91539, 'HP:0012103', 'Abnormality of the mitochondrion', 'XPO:0101326', 'abnormal cementoblast', 0.43478260869565216, 4.8755453832354885, 1.4559540997356917, 'UPHENO:0086172', 'abnormal cell'),
(91540, 'HP:0012103', 'Abnormality of the mitochondrion', 'XPO:0100533', 'abnormal melanoblast', 0.43478260869565216, 4.8755453832354885, 1.4559540997356917, 'UPHENO:0086172', 'abnormal cell'),
(91541, 'HP:0012103', 'Abnormality of the mitochondrion', 'XPO:0101435', 'abnormal paracrine cell', 0.43478260869565216, 4.8755453832354885, 1.4559540997356917, 'UPHENO:0086172', 'abnormal cell'),
(91542, 'HP:0012103', 'Abnormality of the mitochondrion', 'XPO:0100289', 'abnormal chondroblast', 0.43478260869565216, 4.8755453832354885, 1.4559540997356917, 'UPHENO:0086172', 'abnormal cell'),
(91543, 'HP:0012103', 'Abnormality of the mitochondrion', 'XPO:0100976', 'abnormal multiciliated cell', 0.4166666666666667, 4.8755453832354885, 1.4252990012677296, 'UPHENO:0086172', 'abnormal cell'),
(91544, 'HP:0012103', 'Abnormality of the mitochondrion', 'XPO:0100545', 'abnormal male organism', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(91545, 'HP:0012103', 'Abnormality of the mitochondrion', 'XPO:0100704', 'abnormal Merkel cell', 0.43478260869565216, 4.8755453832354885, 1.4559540997356917, 'UPHENO:0086172', 'abnormal cell'),
(91546, 'HP:0012103', 'Abnormality of the mitochondrion', 'XPO:0100084', 'abnormal anatomical group', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(91547, 'HP:0012103', 'Abnormality of the mitochondrion', 'XPO:0107260', 'abnormal anterior-posterior axis', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(91548, 'HP:0012103', 'Abnormality of the mitochondrion', 'XPO:0100285', 'abnormal progenitor cell', 0.43478260869565216, 4.8755453832354885, 1.4559540997356917, 'UPHENO:0086172', 'abnormal cell'),
(91549, 'HP:0012103', 'Abnormality of the mitochondrion', 'XPO:0101157', 'abnormal female organism', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(91550, 'HP:0012103', 'Abnormality of the mitochondrion', 'XPO:0100006', 'abnormal anatomical structure', 0.45, 1.7901636446558942, 0.8975375424432965, 'UPHENO:0002536', 'abnormal anatomical entity'),
(91551, 'HP:0012103', 'Abnormality of the mitochondrion', 'XPO:0100337', 'abnormal zygote', 0.43478260869565216, 4.8755453832354885, 1.4559540997356917, 'UPHENO:0086172', 'abnormal cell'),
(91552, 'HP:0012103', 'Abnormality of the mitochondrion', 'XPO:0101333', 'abnormal barrier epithelial cell', 0.43478260869565216, 4.8755453832354885, 1.4559540997356917, 'UPHENO:0086172', 'abnormal cell'),
(91553, 'HP:0012103', 'Abnormality of the mitochondrion', 'XPO:0100010', 'abnormal multicellular anatomical structure', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(91554, 'HP:0012103', 'Abnormality of the mitochondrion', 'XPO:0101535', 'abnormal absorptive cell', 0.43478260869565216, 4.8755453832354885, 1.4559540997356917, 'UPHENO:0086172', 'abnormal cell'),
(91555, 'HP:0012103', 'Abnormality of the mitochondrion', 'XPO:0100026', 'abnormal germ cell', 0.43478260869565216, 4.8755453832354885, 1.4559540997356917, 'UPHENO:0086172', 'abnormal cell'),
(91556, 'HP:0012103', 'Abnormality of the mitochondrion', 'XPO:0100626', 'abnormal primordial germ cell', 0.4166666666666667, 4.8755453832354885, 1.4252990012677296, 'UPHENO:0086172', 'abnormal cell'),
(91557, 'HP:0012103', 'Abnormality of the mitochondrion', 'XPO:0101547', 'abnormal lampbrush chromosome', 0.4166666666666667, 4.8755453832354885, 1.4252990012677296, 'UPHENO:0086172', 'abnormal cell'),
(91558, 'HP:0012103', 'Abnormality of the mitochondrion', 'XPO:0100423', 'abnormal process', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(91559, 'HP:0012103', 'Abnormality of the mitochondrion', 'XPO:0101467', 'abnormal alkali secreting cell', 0.43478260869565216, 4.8755453832354885, 1.4559540997356917, 'UPHENO:0086172', 'abnormal cell'),
(91560, 'HP:0012103', 'Abnormality of the mitochondrion', 'XPO:0100902', 'abnormal spermatocyte', 0.4166666666666667, 4.8755453832354885, 1.4252990012677296, 'UPHENO:0086172', 'abnormal cell'),
(91561, 'HP:0012103', 'Abnormality of the mitochondrion', 'XPO:0100724', 'abnormal kinetochore', 0.4166666666666667, 4.8755453832354885, 1.4252990012677296, 'UPHENO:0086172', 'abnormal cell'),
(91562, 'HP:0012103', 'Abnormality of the mitochondrion', 'XPO:0100888', 'abnormal microtubule', 0.4166666666666667, 4.8755453832354885, 1.4252990012677296, 'UPHENO:0086172', 'abnormal cell'),
(91563, 'HP:0012103', 'Abnormality of the mitochondrion', 'XPO:0100481', 'abnormal anatomical line', 0.45, 1.7901636446558942, 0.8975375424432965, 'UPHENO:0002536', 'abnormal anatomical entity'),
(91564, 'HP:0012103', 'Abnormality of the mitochondrion', 'XPO:0100573', 'abnormal extraembryonic structure', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(91565, 'HP:0012103', 'Abnormality of the mitochondrion', 'XPO:0100754', 'abnormal electrically active cell', 0.43478260869565216, 4.8755453832354885, 1.4559540997356917, 'UPHENO:0086172', 'abnormal cell'),
(91566, 'HP:0012103', 'Abnormality of the mitochondrion', 'XPO:0115505', 'dead whole organism', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(91567, 'HP:0012103', 'Abnormality of the mitochondrion', 'XPO:0107258', 'abnormal anatomical axis', 0.42857142857142855, 1.7901636446558942, 0.8759069531444602, 'UPHENO:0002536', 'abnormal anatomical entity'),
(91568, 'HP:0012103', 'Abnormality of the mitochondrion', 'XPO:0101228', 'abnormal mesenchymal stem cell', 0.4166666666666667, 4.8755453832354885, 1.4252990012677296, 'UPHENO:0086172', 'abnormal cell'),
(91569, 'HP:0012103', 'Abnormality of the mitochondrion', 'XPO:0131667', 'abnormal actin cytoskeleton', 0.4166666666666667, 4.8755453832354885, 1.4252990012677296, 'UPHENO:0086172', 'abnormal cell'),
(91570, 'HP:0012103', 'Abnormality of the mitochondrion', 'XPO:0100791', 'abnormal multiciliated cell precursor', 0.43478260869565216, 4.8755453832354885, 1.4559540997356917, 'UPHENO:0086172', 'abnormal cell'),
(91571, 'HP:0012103', 'Abnormality of the mitochondrion', 'XPO:0100258', 'abnormal organ part', 0.42857142857142855, 1.7901636446558942, 0.8759069531444602, 'UPHENO:0002536', 'abnormal anatomical entity'),
(91572, 'HP:0012103', 'Abnormality of the mitochondrion', 'XPO:0141499', 'abnormal tadpole', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(91573, 'HP:0012103', 'Abnormality of the mitochondrion', 'XPO:0101513', 'abnormal basal body', 0.4166666666666667, 4.8755453832354885, 1.4252990012677296, 'UPHENO:0086172', 'abnormal cell'),
(91574, 'HP:0012103', 'Abnormality of the mitochondrion', 'XPO:00000000', 'Xenopus phenotype', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91575, 'HP:0012103', 'Abnormality of the mitochondrion', 'XPO:0115509', 'abnormally semi-viable whole organism', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(91576, 'HP:0012103', 'Abnormality of the mitochondrion', 'XPO:0101297', 'abnormal barrier cell', 0.43478260869565216, 4.8755453832354885, 1.4559540997356917, 'UPHENO:0086172', 'abnormal cell'),
(91577, 'HP:0012103', 'Abnormality of the mitochondrion', 'XPO:0100894', 'abnormal nucleus', 0.4166666666666667, 4.8755453832354885, 1.4252990012677296, 'UPHENO:0086172', 'abnormal cell'),
(91578, 'HP:0012103', 'Abnormality of the mitochondrion', 'XPO:0100721', 'abnormal centromere', 0.4166666666666667, 4.8755453832354885, 1.4252990012677296, 'UPHENO:0086172', 'abnormal cell'),
(91579, 'HP:0012103', 'Abnormality of the mitochondrion', 'XPO:0100546', 'abnormal whole organism', 0.42857142857142855, 1.7901636446558942, 0.8759069531444602, 'UPHENO:0002536', 'abnormal anatomical entity'),
(91580, 'HP:0012103', 'Abnormality of the mitochondrion', 'XPO:0100308', 'abnormal early embryonic cell', 0.4166666666666667, 4.8755453832354885, 1.4252990012677296, 'UPHENO:0086172', 'abnormal cell'),
(91581, 'HP:0012103', 'Abnormality of the mitochondrion', 'XPO:0107270', 'abnormal proximal-distal axis', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(91582, 'HP:0012103', 'Abnormality of the mitochondrion', 'XPO:0100477', 'abnormal pericyte', 0.43478260869565216, 4.8755453832354885, 1.4559540997356917, 'UPHENO:0086172', 'abnormal cell'),
(91583, 'HP:0012103', 'Abnormality of the mitochondrion', 'XPO:0101241', 'abnormal nucleate erythrocyte', 0.43478260869565216, 4.8755453832354885, 1.4559540997356917, 'UPHENO:0086172', 'abnormal cell'),
(91584, 'HP:0012103', 'Abnormality of the mitochondrion', 'XPO:0101110', 'abnormal cell-free extract', 0.42857142857142855, 1.7901636446558942, 0.8759069531444602, 'UPHENO:0002536', 'abnormal anatomical entity'),
(91585, 'HP:0012103', 'Abnormality of the mitochondrion', 'XPO:0101141', 'abnormal Keller explant', 0.42857142857142855, 1.7901636446558942, 0.8759069531444602, 'UPHENO:0002536', 'abnormal anatomical entity'),
(91586, 'HP:0012103', 'Abnormality of the mitochondrion', 'XPO:0101071', 'abnormal endoplasmic reticulum', 0.4166666666666667, 4.8755453832354885, 1.4252990012677296, 'UPHENO:0086172', 'abnormal cell'),
(91587, 'HP:0011034', 'Amyloidosis', 'XPO:0141787', 'abnormal hormone metabolic process', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91588, 'HP:0011034', 'Amyloidosis', 'XPO:0101297', 'abnormal barrier cell', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91589, 'HP:0011034', 'Amyloidosis', 'XPO:0115509', 'abnormally semi-viable whole organism', 0.47058823529411764, 1.6758249395539064, 0.8880447629295182, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91590, 'HP:0011034', 'Amyloidosis', 'XPO:0132054', 'abnormal development of portion of organism substance', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91591, 'HP:0011034', 'Amyloidosis', 'XPO:0100728', 'abnormal cell condensation', 0.47058823529411764, 1.6758249395539064, 0.8880447629295182, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91592, 'HP:0011034', 'Amyloidosis', 'XPO:0101200', 'abnormal joint region', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91593, 'HP:0011034', 'Amyloidosis', 'XPO:0141744', 'abnormal chemical homeostasis', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91594, 'HP:0011034', 'Amyloidosis', 'XPO:0100665', 'abnormal egg jelly', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91595, 'HP:0011034', 'Amyloidosis', 'XPO:0100172', 'abnormal stem cell', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91596, 'HP:0011034', 'Amyloidosis', 'XPO:0131722', 'abnormal determination of left/right symmetry', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91597, 'HP:0011034', 'Amyloidosis', 'XPO:0133388', 'absent insulin receptor signaling pathway', 0.47058823529411764, 1.6758249395539064, 0.8880447629295182, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91598, 'HP:0011034', 'Amyloidosis', 'XPO:0131738', 'abnormal Wnt signaling pathway', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91599, 'HP:0011034', 'Amyloidosis', 'XPO:0133403', 'abnormal developmental process', 0.47058823529411764, 1.6758249395539064, 0.8880447629295182, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91600, 'HP:0011034', 'Amyloidosis', 'XPO:0141760', 'abnormal multicellular organismal homeostasis', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91601, 'HP:0011034', 'Amyloidosis', 'XPO:0100268', 'abnormal circulatory system', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91602, 'HP:0011034', 'Amyloidosis', 'XPO:0133397', 'abnormal insulin receptor signaling pathway', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91603, 'HP:0011034', 'Amyloidosis', 'XPO:0141815', 'abnormal isomerase activity', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91604, 'HP:0011034', 'Amyloidosis', 'XPO:0131691', 'abnormal molecular function', 0.5333333333333333, 1.6758249395539064, 0.9453958435996092, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91605, 'HP:0011034', 'Amyloidosis', 'XPO:0103783', 'absent hatching behavior', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91606, 'HP:0011034', 'Amyloidosis', 'XPO:0131470', 'abnormal heart contraction', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91607, 'HP:0011034', 'Amyloidosis', 'XPO:0131480', 'absent mating behavior', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91608, 'HP:0011034', 'Amyloidosis', 'XPO:0100202', 'abnormal embryo', 0.47058823529411764, 1.6758249395539064, 0.8880447629295182, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91609, 'HP:0011034', 'Amyloidosis', 'XPO:0141963', 'absent cilium motility in pronephric nephrostome', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91610, 'HP:0011034', 'Amyloidosis', 'XPO:0100282', 'abnormal pelvic girdle primordium', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91611, 'HP:0011034', 'Amyloidosis', 'XPO:0141960', 'absent cilium motility in brain', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91612, 'HP:0011034', 'Amyloidosis', 'XPO:0101406', 'abnormal cleavage furrow', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91613, 'HP:0011034', 'Amyloidosis', 'XPO:0107264', 'abnormal anterior side', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91614, 'HP:0011034', 'Amyloidosis', 'XPO:0100653', 'abnormal myoblast', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91615, 'HP:0011034', 'Amyloidosis', 'XPO:0131714', 'abnormal establishment of tissue polarity', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91616, 'HP:0011034', 'Amyloidosis', 'XPO:0107258', 'abnormal anatomical axis', 0.5, 1.6758249395539064, 0.9153755894587495, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91617, 'HP:0011034', 'Amyloidosis', 'XPO:0142056', 'abnormal main body axis', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91618, 'HP:0011034', 'Amyloidosis', 'XPO:0141854', 'abnormal glutathione metabolic process', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91619, 'HP:0011034', 'Amyloidosis', 'XPO:0131476', 'absent mechanosensory behavior', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91620, 'HP:0011034', 'Amyloidosis', 'XPO:0100151', 'abnormal primordium', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91621, 'HP:0011034', 'Amyloidosis', 'XPO:0141810', 'abnormal cyclase activity', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91622, 'HP:0011034', 'Amyloidosis', 'XPO:0116429', 'abnormal behavior', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91623, 'HP:0011034', 'Amyloidosis', 'XPO:0141817', 'abnormal demethylase activity', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91624, 'HP:0011034', 'Amyloidosis', 'XPO:0141814', 'abnormal lyase activity', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91625, 'HP:0011034', 'Amyloidosis', 'XPO:0100277', 'abnormal blastocoel', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91626, 'HP:0011034', 'Amyloidosis', 'XPO:0131730', 'abnormal regulation of protein folding', 0.47058823529411764, 1.6758249395539064, 0.8880447629295182, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91627, 'HP:0011034', 'Amyloidosis', 'XPO:0141748', 'abnormal gas homeostasis', 0.5714285714285714, 1.6758249395539064, 0.9785776674202517, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91628, 'HP:0011034', 'Amyloidosis', 'XPO:0131703', 'abnormal cell division', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91629, 'HP:0011034', 'Amyloidosis', 'XPO:0131482', 'absent locomotory behavior', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91630, 'HP:0011034', 'Amyloidosis', 'XPO:0101411', 'abnormal marginal zone (sensu neural)', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91631, 'HP:0011034', 'Amyloidosis', 'XPO:0141975', 'abnormal cilium motility', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91632, 'HP:0011034', 'Amyloidosis', 'XPO:0100162', 'abnormal presumptive rhombomere', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91633, 'HP:0011034', 'Amyloidosis', 'XPO:0100363', 'abnormal cardiovascular system', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91634, 'HP:0011034', 'Amyloidosis', 'XPO:0141272', 'absent surface breathing', 0.5714285714285714, 1.6758249395539064, 0.9785776674202517, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91635, 'HP:0011034', 'Amyloidosis', 'XPO:0131723', 'abnormal pathway-restricted SMAD protein phosphorylation', 0.5714285714285714, 1.6758249395539064, 0.9785776674202517, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91636, 'HP:0011034', 'Amyloidosis', 'XPO:0100856', 'abnormal simple organ', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91637, 'HP:0011034', 'Amyloidosis', 'XPO:0141784', 'abnormal cellular hormone metabolic process', 0.5714285714285714, 1.6758249395539064, 0.9785776674202517, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91638, 'HP:0011034', 'Amyloidosis', 'XPO:0115508', 'abnormally peramorphic growth of whole organism', 0.47058823529411764, 1.6758249395539064, 0.8880447629295182, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91639, 'HP:0011034', 'Amyloidosis', 'XPO:0141315', 'abnormal anatomical region', 0.47058823529411764, 1.6758249395539064, 0.8880447629295182, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91640, 'HP:0011034', 'Amyloidosis', 'XPO:0101326', 'abnormal cementoblast', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91641, 'HP:0011034', 'Amyloidosis', 'XPO:0100610', 'abnormal appendage', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91642, 'HP:0011034', 'Amyloidosis', 'XPO:0141276', 'decreased surface breathing', 0.5333333333333333, 1.6758249395539064, 0.9453958435996092, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91643, 'HP:0011034', 'Amyloidosis', 'XPO:0141600', 'absent metamorphosis', 0.47058823529411764, 1.6758249395539064, 0.8880447629295182, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91644, 'HP:0011034', 'Amyloidosis', 'XPO:0141796', 'abnormal demethylation', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91645, 'HP:0011034', 'Amyloidosis', 'XPO:0141818', 'abnormal peptidoglycan muralytic activity', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91646, 'HP:0011034', 'Amyloidosis', 'XPO:0131798', 'abnormal development of anatomical space', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91647, 'HP:0011034', 'Amyloidosis', 'XPO:0141958', 'absent cilium motility in left-right organizer', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91648, 'HP:0011034', 'Amyloidosis', 'XPO:0141777', 'abnormal catabolic process', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91649, 'HP:0011034', 'Amyloidosis', 'XPO:0100802', 'abnormal exocrine cell', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91650, 'HP:0011034', 'Amyloidosis', 'XPO:0131740', 'abnormal detection of nodal flow', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91651, 'HP:0011034', 'Amyloidosis', 'XPO:0115505', 'dead whole organism', 0.47058823529411764, 1.6758249395539064, 0.8880447629295182, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91652, 'HP:0011034', 'Amyloidosis', 'XPO:0107268', 'abnormal left side', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91653, 'HP:0011034', 'Amyloidosis', 'XPO:0107260', 'abnormal anterior-posterior axis', 0.47058823529411764, 1.6758249395539064, 0.8880447629295182, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91654, 'HP:0011034', 'Amyloidosis', 'XPO:0101132', 'abnormal apoptotic cell', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91655, 'HP:0011034', 'Amyloidosis', 'XPO:0100423', 'abnormal process', 0.47058823529411764, 1.6758249395539064, 0.8880447629295182, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91656, 'HP:0011034', 'Amyloidosis', 'XPO:0141871', 'abnormal cadaverine transport', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91657, 'HP:0011034', 'Amyloidosis', 'XPO:0107272', 'abnormal axial region', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91658, 'HP:0011034', 'Amyloidosis', 'XPO:0131472', 'absent vocalization behavior', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91659, 'HP:0011034', 'Amyloidosis', 'XPO:0100337', 'abnormal zygote', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91660, 'HP:0011034', 'Amyloidosis', 'XPO:0107265', 'abnormal posterior side', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91661, 'HP:0011034', 'Amyloidosis', 'XPO:0131474', 'absent behavioral response to pain', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91662, 'HP:0011034', 'Amyloidosis', 'XPO:0131715', 'abnormal fibroblast growth factor receptor signaling pathway', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91663, 'HP:0011034', 'Amyloidosis', 'XPO:0101467', 'abnormal alkali secreting cell', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91664, 'HP:0011034', 'Amyloidosis', 'XPO:0100014', 'abnormal tissue', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91665, 'HP:0011034', 'Amyloidosis', 'XPO:0100915', 'abnormal dermal system', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91666, 'HP:0011034', 'Amyloidosis', 'XPO:0100549', 'abnormal mitotic cell', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91667, 'HP:0011034', 'Amyloidosis', 'XPO:0100006', 'abnormal anatomical structure', 0.5333333333333333, 1.6758249395539064, 0.9453958435996092, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91668, 'HP:0011034', 'Amyloidosis', 'XPO:0100023', 'abnormal mesenchyme', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91669, 'HP:0011034', 'Amyloidosis', 'XPO:0100231', 'abnormal compound organ', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91670, 'HP:0011034', 'Amyloidosis', 'XPO:0141267', 'abnormal resting posture', 0.5714285714285714, 1.6758249395539064, 0.9785776674202517, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91671, 'HP:0011034', 'Amyloidosis', 'XPO:0100010', 'abnormal multicellular anatomical structure', 0.47058823529411764, 1.6758249395539064, 0.8880447629295182, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91672, 'HP:0011034', 'Amyloidosis', 'XPO:0141816', 'abnormal ligase activity', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91673, 'HP:0011034', 'Amyloidosis', 'XPO:0141754', 'abnormal homeostatic process', 0.47058823529411764, 1.6758249395539064, 0.8880447629295182, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91674, 'HP:0011034', 'Amyloidosis', 'XPO:0100258', 'abnormal organ part', 0.5, 1.6758249395539064, 0.9153755894587495, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91675, 'HP:0011034', 'Amyloidosis', 'XPO:0141962', 'absent cilium motility in pronephric kidney', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91676, 'HP:0011034', 'Amyloidosis', 'XPO:0100715', 'abnormal ciliated cell', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91677, 'HP:0011034', 'Amyloidosis', 'XPO:0141743', 'abnormal chemical homeostasis within a tissue', 0.5714285714285714, 1.6758249395539064, 0.9785776674202517, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91678, 'HP:0011034', 'Amyloidosis', 'XPO:0107271', 'abnormal apical region', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91679, 'HP:0011034', 'Amyloidosis', 'XPO:0141715', 'abnormal septum', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91680, 'HP:0011034', 'Amyloidosis', 'XPO:0100481', 'abnormal anatomical line', 0.5333333333333333, 1.6758249395539064, 0.9453958435996092, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91681, 'HP:0011034', 'Amyloidosis', 'XPO:0107259', 'abnormal animal-vegetal axis', 0.47058823529411764, 1.6758249395539064, 0.8880447629295182, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91682, 'HP:0011034', 'Amyloidosis', 'XPO:0101347', 'abnormal hindlimb region', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91683, 'HP:0011034', 'Amyloidosis', 'XPO:0141964', 'absent cilium motility in olfactory pit', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91684, 'HP:0011034', 'Amyloidosis', 'XPO:0101570', 'abnormal forelimb region', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91685, 'HP:0011034', 'Amyloidosis', 'XPO:0100295', 'abnormal extracellular matrix', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91686, 'HP:0011034', 'Amyloidosis', 'XPO:0141770', 'abnormal urate homeostasis', 0.5714285714285714, 1.6758249395539064, 0.9785776674202517, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91687, 'HP:0011034', 'Amyloidosis', 'XPO:0131481', 'absent feeding behavior', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91688, 'HP:0011034', 'Amyloidosis', 'XPO:0131477', 'absent visual behavior', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91689, 'HP:0011034', 'Amyloidosis', 'XPO:0100781', 'abnormal presumptive ectoderm', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91690, 'HP:0011034', 'Amyloidosis', 'XPO:0100239', 'abnormal acellular anatomical structure', 0.47058823529411764, 1.6758249395539064, 0.8880447629295182, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91691, 'HP:0011034', 'Amyloidosis', 'XPO:0133401', 'absent determination of left/right symmetry in lateral plate mesoderm', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91692, 'HP:0011034', 'Amyloidosis', 'XPO:0100638', 'abnormal polar body', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91693, 'HP:0011034', 'Amyloidosis', 'XPO:0100546', 'abnormal whole organism', 0.5, 1.6758249395539064, 0.9153755894587495, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91694, 'HP:0011034', 'Amyloidosis', 'XPO:0141792', 'abnormal small molecule metabolic process', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91695, 'HP:0011034', 'Amyloidosis', 'XPO:0131469', 'abnormal heart process', 0.47058823529411764, 1.6758249395539064, 0.8880447629295182, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91696, 'HP:0011034', 'Amyloidosis', 'XPO:0100912', 'abnormal trabecula', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91697, 'HP:0011034', 'Amyloidosis', 'XPO:0101040', 'abnormal axial mesoderm', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91698, 'HP:0011034', 'Amyloidosis', 'XPO:0141812', 'abnormal transferase activity', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91699, 'HP:0011034', 'Amyloidosis', 'XPO:0100081', 'abnormal anatomical entity in vitro', 0.5333333333333333, 1.6758249395539064, 0.9453958435996092, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91700, 'HP:0011034', 'Amyloidosis', 'XPO:0141778', 'abnormal biosynthetic process', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91701, 'HP:0011034', 'Amyloidosis', 'XPO:0116434', 'abnormal biological process', 0.5333333333333333, 1.6758249395539064, 0.9453958435996092, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91702, 'HP:0011034', 'Amyloidosis', 'XPO:0116494', 'absent biological process', 0.5333333333333333, 1.6758249395539064, 0.9453958435996092, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91703, 'HP:0011034', 'Amyloidosis', 'XPO:0131711', 'abnormal establishment of cell polarity', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91704, 'HP:0011034', 'Amyloidosis', 'XPO:0131475', 'absent olfactory behavior', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91705, 'HP:0011034', 'Amyloidosis', 'XPO:0141791', 'abnormal primary metabolic process', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91706, 'HP:0011034', 'Amyloidosis', 'XPO:0100108', 'abnormal cell part', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91707, 'HP:0011034', 'Amyloidosis', 'XPO:0131721', 'abnormal nodal signaling pathway', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91708, 'HP:0011034', 'Amyloidosis', 'XPO:0101435', 'abnormal paracrine cell', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91709, 'HP:0011034', 'Amyloidosis', 'XPO:0100754', 'abnormal electrically active cell', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91710, 'HP:0011034', 'Amyloidosis', 'XPO:0100186', 'abnormal uveal tract', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91711, 'HP:0011034', 'Amyloidosis', 'XPO:0100531', 'abnormal proliferative region', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91712, 'HP:0011034', 'Amyloidosis', 'XPO:0100009', 'abnormal multi-tissue structure', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91713, 'HP:0011034', 'Amyloidosis', 'XPO:0100786', 'abnormal presumptive axial mesoderm', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91714, 'HP:0011034', 'Amyloidosis', 'XPO:0100573', 'abnormal extraembryonic structure', 0.47058823529411764, 1.6758249395539064, 0.8880447629295182, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91715, 'HP:0011034', 'Amyloidosis', 'XPO:0141811', 'abnormal oxidoreductase activity', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91716, 'HP:0011034', 'Amyloidosis', 'XPO:0100643', 'abnormal thoracic region', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91717, 'HP:0011034', 'Amyloidosis', 'XPO:0141794', 'abnormal prosthetic group metabolic process', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91718, 'HP:0011034', 'Amyloidosis', 'XPO:0141959', 'absent cilium motility in floor plate', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91719, 'HP:0011034', 'Amyloidosis', 'XPO:0141771', 'abnormal urea homeostasis', 0.5714285714285714, 1.6758249395539064, 0.9785776674202517, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91720, 'HP:0011034', 'Amyloidosis', 'XPO:0141745', 'abnormal creatinine homeostasis', 0.5714285714285714, 1.6758249395539064, 0.9785776674202517, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91721, 'HP:0011034', 'Amyloidosis', 'XPO:0131744', 'abnormal apical constriction', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91722, 'HP:0011034', 'Amyloidosis', 'XPO:0141738', 'abnormal carbon dioxide homeostasis', 0.5714285714285714, 1.6758249395539064, 0.9785776674202517, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91723, 'HP:0011034', 'Amyloidosis', 'XPO:0100060', 'abnormal regenerating tissue', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91724, 'HP:0011034', 'Amyloidosis', 'XPO:0100742', 'abnormal musculoskeletal system', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91725, 'HP:0011034', 'Amyloidosis', 'XPO:0131975', 'abnormal development of anatomical line', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91726, 'HP:0011034', 'Amyloidosis', 'XPO:0101004', 'abnormal acid secreting cell', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91727, 'HP:0011034', 'Amyloidosis', 'XPO:0100344', 'abnormal portion of organism substance', 0.5333333333333333, 1.6758249395539064, 0.9453958435996092, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91728, 'HP:0011034', 'Amyloidosis', 'XPO:0100293', 'abnormal duct', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91729, 'HP:0011034', 'Amyloidosis', 'XPO:0100003', 'abnormal organism subdivision', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91730, 'HP:0011034', 'Amyloidosis', 'XPO:0107262', 'abnormal left-right axis', 0.47058823529411764, 1.6758249395539064, 0.8880447629295182, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91731, 'HP:0011034', 'Amyloidosis', 'XPO:0131765', 'abnormal development of anatomical region', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91732, 'HP:0011034', 'Amyloidosis', 'XPO:0100852', 'abnormal interdigital region', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91733, 'HP:0011034', 'Amyloidosis', 'XPO:0131705', 'abnormal chemotaxis', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91734, 'HP:0011034', 'Amyloidosis', 'XPO:0141266', 'abnormal surface breathing', 0.5714285714285714, 1.6758249395539064, 0.9785776674202517, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91735, 'HP:0011034', 'Amyloidosis', 'XPO:0101078', 'abnormal mucous gland', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91736, 'HP:0011034', 'Amyloidosis', 'XPO:0100477', 'abnormal pericyte', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91737, 'HP:0011034', 'Amyloidosis', 'XPO:0115512', 'abnormally semi-erect whole organism', 0.47058823529411764, 1.6758249395539064, 0.8880447629295182, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91738, 'HP:0011034', 'Amyloidosis', 'XPO:0100667', 'abnormal vegetal yolk mass', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91739, 'HP:0011034', 'Amyloidosis', 'XPO:0100384', 'abnormal amputated tissue', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91740, 'HP:0011034', 'Amyloidosis', 'XPO:0101241', 'abnormal nucleate erythrocyte', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91741, 'HP:0011034', 'Amyloidosis', 'XPO:0100104', 'abnormal embryonic structure', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91742, 'HP:0011034', 'Amyloidosis', 'XPO:0100004', 'abnormal cell', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91743, 'HP:0011034', 'Amyloidosis', 'XPO:0100557', 'abnormal prime meridian', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91744, 'HP:0011034', 'Amyloidosis', 'XPO:0101237', 'abnormal mucus secreting cell', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91745, 'HP:0011034', 'Amyloidosis', 'XPO:0131729', 'abnormal regulation of growth rate', 0.47058823529411764, 1.6758249395539064, 0.8880447629295182, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91746, 'HP:0011034', 'Amyloidosis', 'XPO:0100913', 'abnormal Brachets cleft', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91747, 'HP:0011034', 'Amyloidosis', 'XPO:0141271', 'increased surface breathing', 0.5333333333333333, 1.6758249395539064, 0.9453958435996092, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91748, 'HP:0011034', 'Amyloidosis', 'XPO:0100762', 'abnormal intersomitic region', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91749, 'HP:0011034', 'Amyloidosis', 'XPO:0100394', 'abnormal marginal zone', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91750, 'HP:0011034', 'Amyloidosis', 'XPO:0100251', 'abnormal proteinaceous extracellular matrix', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91751, 'HP:0011034', 'Amyloidosis', 'XPO:0100969', 'abnormal disaggregated/reaggregated ectoderm treated with activin', 0.5, 1.6758249395539064, 0.9153755894587495, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91752, 'HP:0011034', 'Amyloidosis', 'XPO:0141813', 'abnormal hydrolase activity', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91753, 'HP:0011034', 'Amyloidosis', 'XPO:0107278', 'abnormal medial region', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91754, 'HP:0011034', 'Amyloidosis', 'XPO:0131479', 'absent social behavior', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91755, 'HP:0011034', 'Amyloidosis', 'XPO:0100062', 'abnormal anatomical space', 0.47058823529411764, 1.6758249395539064, 0.8880447629295182, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91756, 'HP:0011034', 'Amyloidosis', 'XPO:0101373', 'abnormal oxygen accumulating cell', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91757, 'HP:0011034', 'Amyloidosis', 'XPO:0141783', 'abnormal collagen metabolic process', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91758, 'HP:0011034', 'Amyloidosis', 'XPO:0141265', 'abnormal escape behavior', 0.5714285714285714, 1.6758249395539064, 0.9785776674202517, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91759, 'HP:0011034', 'Amyloidosis', 'XPO:0100192', 'abnormal epithelium', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91760, 'HP:0011034', 'Amyloidosis', 'XPO:0100084', 'abnormal anatomical group', 0.47058823529411764, 1.6758249395539064, 0.8880447629295182, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91761, 'HP:0011034', 'Amyloidosis', 'XPO:00000000', 'Xenopus phenotype', 0.6153846153846154, 1.6758249395539064, 1.0155180381851063, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91762, 'HP:0011034', 'Amyloidosis', 'XPO:0141781', 'abnormal secondary metabolic process', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91763, 'HP:0011034', 'Amyloidosis', 'XPO:0107263', 'abnormal anatomical side', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91764, 'HP:0011034', 'Amyloidosis', 'XPO:0131728', 'abnormal regulation of cell size', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91765, 'HP:0011034', 'Amyloidosis', 'XPO:0101157', 'abnormal female organism', 0.47058823529411764, 1.6758249395539064, 0.8880447629295182, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91766, 'HP:0011034', 'Amyloidosis', 'XPO:0141499', 'abnormal tadpole', 0.47058823529411764, 1.6758249395539064, 0.8880447629295182, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91767, 'HP:0011034', 'Amyloidosis', 'XPO:0101535', 'abnormal absorptive cell', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91768, 'HP:0011034', 'Amyloidosis', 'XPO:0141775', 'abnormal nitrogen compound metabolic process', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91769, 'HP:0011034', 'Amyloidosis', 'XPO:0107266', 'abnormal dorsal side', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91770, 'HP:0011034', 'Amyloidosis', 'XPO:0100991', 'abnormal iliac process primordium', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91771, 'HP:0011034', 'Amyloidosis', 'XPO:0131700', 'abnormal BMP signaling pathway', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91772, 'HP:0011034', 'Amyloidosis', 'XPO:0141904', 'abnormal glucosamine metabolic process', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91773, 'HP:0011034', 'Amyloidosis', 'XPO:0101333', 'abnormal barrier epithelial cell', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91774, 'HP:0011034', 'Amyloidosis', 'XPO:0141797', 'abnormal hydrogen metabolic process', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91775, 'HP:0011034', 'Amyloidosis', 'XPO:0141782', 'abnormal methylation', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91776, 'HP:0011034', 'Amyloidosis', 'XPO:0141724', 'abnormal prevention of polyspermy', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91777, 'HP:0011034', 'Amyloidosis', 'XPO:0101569', 'abnormal activin-induced ectoderm', 0.5, 1.6758249395539064, 0.9153755894587495, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91778, 'HP:0011034', 'Amyloidosis', 'XPO:0141795', 'abnormal glycosylation', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91779, 'HP:0011034', 'Amyloidosis', 'XPO:0101448', 'abnormal myelin accumulating cell', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91780, 'HP:0011034', 'Amyloidosis', 'XPO:0107267', 'abnormal ventral side', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91781, 'HP:0011034', 'Amyloidosis', 'XPO:0141809', 'abnormal catalytic activity', 0.47058823529411764, 1.6758249395539064, 0.8880447629295182, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91782, 'HP:0011034', 'Amyloidosis', 'XPO:0100807', 'abnormal matrix-based tissue', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91783, 'HP:0011034', 'Amyloidosis', 'XPO:0116433', 'abnormal axis specification', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91784, 'HP:0011034', 'Amyloidosis', 'XPO:0100070', 'abnormal anatomical system', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91785, 'HP:0011034', 'Amyloidosis', 'XPO:0101110', 'abnormal cell-free extract', 0.5, 1.6758249395539064, 0.9153755894587495, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91786, 'HP:0011034', 'Amyloidosis', 'XPO:0131719', 'abnormal activation of meiosis', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91787, 'HP:0011034', 'Amyloidosis', 'XPO:0141772', 'abnormal water homeostasis', 0.5714285714285714, 1.6758249395539064, 0.9785776674202517, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91788, 'HP:0011034', 'Amyloidosis', 'XPO:0107270', 'abnormal proximal-distal axis', 0.47058823529411764, 1.6758249395539064, 0.8880447629295182, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91789, 'HP:0011034', 'Amyloidosis', 'XPO:0100545', 'abnormal male organism', 0.47058823529411764, 1.6758249395539064, 0.8880447629295182, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91790, 'HP:0011034', 'Amyloidosis', 'XPO:0133340', 'abnormal cell adhesion', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91791, 'HP:0011034', 'Amyloidosis', 'XPO:0100704', 'abnormal Merkel cell', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91792, 'HP:0011034', 'Amyloidosis', 'XPO:0101109', 'abnormal egg cell-free extract', 0.47058823529411764, 1.6758249395539064, 0.8880447629295182, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91793, 'HP:0011034', 'Amyloidosis', 'XPO:0100791', 'abnormal multiciliated cell precursor', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91794, 'HP:0011034', 'Amyloidosis', 'XPO:0131725', 'abnormal phosphorylation of RNA polymerase II C-terminal domain', 0.5714285714285714, 1.6758249395539064, 0.9785776674202517, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91795, 'HP:0011034', 'Amyloidosis', 'XPO:0141263', 'abnormal visually guided collision avoidance behavior', 0.5714285714285714, 1.6758249395539064, 0.9785776674202517, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91796, 'HP:0011034', 'Amyloidosis', 'XPO:0141776', 'abnormal metabolic process', 0.47058823529411764, 1.6758249395539064, 0.8880447629295182, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91797, 'HP:0011034', 'Amyloidosis', 'XPO:0103624', 'absent anterior/posterior pattern specification in midgut', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91798, 'HP:0011034', 'Amyloidosis', 'XPO:0100533', 'abnormal melanoblast', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91799, 'HP:0011034', 'Amyloidosis', 'XPO:0101141', 'abnormal Keller explant', 0.5, 1.6758249395539064, 0.9153755894587495, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91800, 'HP:0011034', 'Amyloidosis', 'XPO:0107269', 'abnormal right side', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91801, 'HP:0011034', 'Amyloidosis', 'XPO:0107273', 'abnormal basal region', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91802, 'HP:0011034', 'Amyloidosis', 'XPO:0100026', 'abnormal germ cell', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91803, 'HP:0011034', 'Amyloidosis', 'XPO:0141264', 'abnormal schooling behavior', 0.5714285714285714, 1.6758249395539064, 0.9785776674202517, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91804, 'HP:0011034', 'Amyloidosis', 'XPO:0100289', 'abnormal chondroblast', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91805, 'HP:0011034', 'Amyloidosis', 'XPO:0100135', 'abnormal surface structure', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91806, 'HP:0011034', 'Amyloidosis', 'XPO:0141961', 'absent cilium motility in mucociliary epithelium', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91807, 'HP:0011034', 'Amyloidosis', 'XPO:0128000', 'absent behavior', 0.47058823529411764, 1.6758249395539064, 0.8880447629295182, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91808, 'HP:0011034', 'Amyloidosis', 'XPO:0133402', 'absent determination of left/right symmetry in alimentary system', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91809, 'HP:0011034', 'Amyloidosis', 'XPO:0107276', 'abnormal dorsal region', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91810, 'HP:0011034', 'Amyloidosis', 'XPO:0100028', 'abnormal anatomical cluster', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91811, 'HP:0011034', 'Amyloidosis', 'XPO:0141786', 'abnormal pigment metabolic process', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91812, 'HP:0011034', 'Amyloidosis', 'XPO:0100339', 'abnormal circumblastoporal collar', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91813, 'HP:0011034', 'Amyloidosis', 'XPO:0131760', 'abnormal development of anatomical structure', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91814, 'HP:0011034', 'Amyloidosis', 'XPO:0107261', 'abnormal dorsal-ventral axis', 0.47058823529411764, 1.6758249395539064, 0.8880447629295182, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91815, 'HP:0011034', 'Amyloidosis', 'XPO:0101519', 'abnormal hypobranchial placode', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91816, 'HP:0011034', 'Amyloidosis', 'XPO:0101503', 'abnormal organ cortex', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91817, 'HP:0011034', 'Amyloidosis', 'XPO:0100285', 'abnormal progenitor cell', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91818, 'HP:0011034', 'Amyloidosis', 'XPO:0100691', 'abnormal keratin accumulating cell', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91819, 'HP:0011034', 'Amyloidosis', 'XPO:0141968', 'absent cilium motility in ciliated cell', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91820, 'HP:0011034', 'Amyloidosis', 'XPO:0141965', 'absent cilium motility in alimentary system', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91821, 'HP:0011034', 'Amyloidosis', 'XPO:0100999', 'abnormal serous membrane', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91822, 'HP:0100243', 'Leiomyosarcoma', 'XPO:0100258', 'abnormal organ part', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91823, 'HP:0100243', 'Leiomyosarcoma', 'XPO:0100481', 'abnormal anatomical line', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91824, 'HP:0100243', 'Leiomyosarcoma', 'XPO:0100006', 'abnormal anatomical structure', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91825, 'HP:0100243', 'Leiomyosarcoma', 'XPO:0141772', 'abnormal water homeostasis', 0.47058823529411764, 1.6758249395539064, 0.8880447629295182, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91826, 'HP:0100243', 'Leiomyosarcoma', 'XPO:0141743', 'abnormal chemical homeostasis within a tissue', 0.47058823529411764, 1.6758249395539064, 0.8880447629295182, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91827, 'HP:0100243', 'Leiomyosarcoma', 'XPO:0101110', 'abnormal cell-free extract', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91828, 'HP:0100243', 'Leiomyosarcoma', 'XPO:0141784', 'abnormal cellular hormone metabolic process', 0.47058823529411764, 1.6758249395539064, 0.8880447629295182, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91829, 'HP:0100243', 'Leiomyosarcoma', 'XPO:0116494', 'absent biological process', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91830, 'HP:0100243', 'Leiomyosarcoma', 'XPO:0107258', 'abnormal anatomical axis', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91831, 'HP:0100243', 'Leiomyosarcoma', 'XPO:0141738', 'abnormal carbon dioxide homeostasis', 0.47058823529411764, 1.6758249395539064, 0.8880447629295182, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91832, 'HP:0100243', 'Leiomyosarcoma', 'XPO:0131725', 'abnormal phosphorylation of RNA polymerase II C-terminal domain', 0.47058823529411764, 1.6758249395539064, 0.8880447629295182, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91833, 'HP:0100243', 'Leiomyosarcoma', 'XPO:0131723', 'abnormal pathway-restricted SMAD protein phosphorylation', 0.47058823529411764, 1.6758249395539064, 0.8880447629295182, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91834, 'HP:0100243', 'Leiomyosarcoma', 'XPO:0141748', 'abnormal gas homeostasis', 0.47058823529411764, 1.6758249395539064, 0.8880447629295182, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91835, 'HP:0100243', 'Leiomyosarcoma', 'XPO:0141271', 'increased surface breathing', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91836, 'HP:0100243', 'Leiomyosarcoma', 'XPO:0141771', 'abnormal urea homeostasis', 0.47058823529411764, 1.6758249395539064, 0.8880447629295182, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91837, 'HP:0100243', 'Leiomyosarcoma', 'XPO:0141265', 'abnormal escape behavior', 0.47058823529411764, 1.6758249395539064, 0.8880447629295182, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91838, 'HP:0100243', 'Leiomyosarcoma', 'XPO:0131691', 'abnormal molecular function', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91839, 'HP:0100243', 'Leiomyosarcoma', 'XPO:0141745', 'abnormal creatinine homeostasis', 0.47058823529411764, 1.6758249395539064, 0.8880447629295182, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91840, 'HP:0100243', 'Leiomyosarcoma', 'XPO:0141267', 'abnormal resting posture', 0.47058823529411764, 1.6758249395539064, 0.8880447629295182, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91841, 'HP:0100243', 'Leiomyosarcoma', 'XPO:0141264', 'abnormal schooling behavior', 0.47058823529411764, 1.6758249395539064, 0.8880447629295182, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91842, 'HP:0100243', 'Leiomyosarcoma', 'XPO:0100081', 'abnormal anatomical entity in vitro', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91843, 'HP:0100243', 'Leiomyosarcoma', 'XPO:0116434', 'abnormal biological process', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91844, 'HP:0100243', 'Leiomyosarcoma', 'XPO:0141272', 'absent surface breathing', 0.47058823529411764, 1.6758249395539064, 0.8880447629295182, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91845, 'HP:0100243', 'Leiomyosarcoma', 'XPO:0141266', 'abnormal surface breathing', 0.47058823529411764, 1.6758249395539064, 0.8880447629295182, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91846, 'HP:0100243', 'Leiomyosarcoma', 'XPO:0101141', 'abnormal Keller explant', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91847, 'HP:0100243', 'Leiomyosarcoma', 'XPO:0100969', 'abnormal disaggregated/reaggregated ectoderm treated with activin', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91848, 'HP:0100243', 'Leiomyosarcoma', 'XPO:0141263', 'abnormal visually guided collision avoidance behavior', 0.47058823529411764, 1.6758249395539064, 0.8880447629295182, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91849, 'HP:0100243', 'Leiomyosarcoma', 'XPO:0100546', 'abnormal whole organism', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91850, 'HP:0100243', 'Leiomyosarcoma', 'XPO:0141276', 'decreased surface breathing', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91851, 'HP:0100243', 'Leiomyosarcoma', 'XPO:0101569', 'abnormal activin-induced ectoderm', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91852, 'HP:0100243', 'Leiomyosarcoma', 'XPO:00000000', 'Xenopus phenotype', 0.5, 1.6758249395539064, 0.9153755894587495, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91853, 'HP:0100243', 'Leiomyosarcoma', 'XPO:0141770', 'abnormal urate homeostasis', 0.47058823529411764, 1.6758249395539064, 0.8880447629295182, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91854, 'HP:0100243', 'Leiomyosarcoma', 'XPO:0100344', 'abnormal portion of organism substance', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91855, 'HP:0005289', 'Abnormal nasolabial region morphology', 'XPO:0101334', 'abnormal olfactory pit', 0.40625, 9.15868676709498, 1.9289158870029393, 'UPHENO:0002907', 'abnormal nose'),
(91856, 'HP:0005289', 'Abnormal nasolabial region morphology', 'XPO:0101483', 'abnormal nostril', 0.40625, 9.15868676709498, 1.9289158870029393, 'UPHENO:0002907', 'abnormal nose'),
(91857, 'HP:0032523', 'Tendon thickening', 'XPO:0101890', 'abnormal organ part morphology', 0.41935483870967744, 3.067140347159989, 1.134116460326373, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(91858, 'HP:0032523', 'Tendon thickening', 'XPO:0102601', 'abnormal disaggregated/reaggregated ectoderm treated with activin morphology', 0.41935483870967744, 3.067140347159989, 1.134116460326373, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(91859, 'HP:0032523', 'Tendon thickening', 'XPO:0101716', 'abnormal anatomical group morphology', 0.40625, 3.067140347159989, 1.1162552423320329, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(91860, 'HP:0032523', 'Tendon thickening', 'XPO:0140144', 'abnormally necrotic portion of organism substance', 0.41935483870967744, 3.067140347159989, 1.134116460326373, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(91861, 'HP:0032523', 'Tendon thickening', 'XPO:0101694', 'abnormal anatomical space morphology', 0.41935483870967744, 3.067140347159989, 1.134116460326373, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(91862, 'HP:0032523', 'Tendon thickening', 'XPO:0102742', 'abnormal cell-free extract morphology', 0.41935483870967744, 3.067140347159989, 1.134116460326373, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(91863, 'HP:0032523', 'Tendon thickening', 'XPO:0101976', 'abnormal portion of organism substance morphology', 0.4482758620689655, 3.067140347159989, 1.1725719522526752, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(91864, 'HP:0032523', 'Tendon thickening', 'XPO:0102055', 'abnormal process morphology', 0.40625, 3.067140347159989, 1.1162552423320329, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(91865, 'HP:0032523', 'Tendon thickening', 'XPO:0141316', 'abnormal anatomical region morphology', 0.41935483870967744, 3.067140347159989, 1.134116460326373, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(91866, 'HP:0032523', 'Tendon thickening', 'XPO:0102217', 'abnormal elastica externa morphology', 0.40540540540540543, 4.825104621810128, 1.3986148488159384, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(91867, 'HP:0032523', 'Tendon thickening', 'XPO:0102178', 'abnormal whole organism morphology', 0.41935483870967744, 3.067140347159989, 1.134116460326373, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(91868, 'HP:0032523', 'Tendon thickening', 'XPO:0102773', 'abnormal Keller explant morphology', 0.41935483870967744, 3.067140347159989, 1.134116460326373, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(91869, 'HP:0032523', 'Tendon thickening', 'XPO:0140269', 'abnormally necrotic anatomical line', 0.41935483870967744, 3.067140347159989, 1.134116460326373, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(91870, 'HP:0032523', 'Tendon thickening', 'XPO:0102113', 'abnormal anatomical line morphology', 0.4482758620689655, 3.067140347159989, 1.1725719522526752, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(91871, 'HP:0032523', 'Tendon thickening', 'XPO:0139718', 'abnormally necrotic anatomical structure', 0.41935483870967744, 3.067140347159989, 1.134116460326373, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(91872, 'HP:0032523', 'Tendon thickening', 'XPO:0115510', 'abnormal degeneration of whole organism', 0.40625, 3.067140347159989, 1.1162552423320329, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(91873, 'HP:0032523', 'Tendon thickening', 'XPO:0101713', 'abnormal anatomical entity in vitro morphology', 0.4482758620689655, 3.067140347159989, 1.1725719522526752, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(91874, 'HP:0032523', 'Tendon thickening', 'XPO:0102360', 'abnormal cell condensation morphology', 0.40625, 3.067140347159989, 1.1162552423320329, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(91875, 'HP:0032523', 'Tendon thickening', 'XPO:0101642', 'abnormal multicellular anatomical structure morphology', 0.40625, 3.067140347159989, 1.1162552423320329, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(91876, 'HP:0032523', 'Tendon thickening', 'XPO:0102097', 'abnormal skeletal system morphology', 0.40540540540540543, 4.825104621810128, 1.3986148488159384, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(91877, 'HP:0032523', 'Tendon thickening', 'XPO:0102010', 'abnormal perichondrium morphology', 0.42105263157894735, 7.212684573300959, 1.742676051461443, 'UPHENO:0002712', 'abnormal connective tissue'),
(91878, 'HP:0032523', 'Tendon thickening', 'XPO:0101871', 'abnormal acellular anatomical structure morphology', 0.40625, 3.067140347159989, 1.1162552423320329, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(91879, 'HP:0032523', 'Tendon thickening', 'XPO:0107345', 'abnormal anatomical axis morphology', 0.41935483870967744, 3.067140347159989, 1.134116460326373, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(91880, 'HP:0032523', 'Tendon thickening', 'XPO:0103201', 'abnormal activin-induced ectoderm morphology', 0.41935483870967744, 3.067140347159989, 1.134116460326373, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(91881, 'HP:0032523', 'Tendon thickening', 'XPO:0101638', 'abnormal anatomical structure morphology', 0.4482758620689655, 3.067140347159989, 1.1725719522526752, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(91882, 'HP:0034861', 'Reduced leukocyte arylsulfatase B activity', 'XPO:0107259', 'abnormal animal-vegetal axis', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91883, 'HP:0034861', 'Reduced leukocyte arylsulfatase B activity', 'XPO:0100010', 'abnormal multicellular anatomical structure', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91884, 'HP:0034861', 'Reduced leukocyte arylsulfatase B activity', 'XPO:0131730', 'abnormal regulation of protein folding', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91885, 'HP:0034861', 'Reduced leukocyte arylsulfatase B activity', 'XPO:0100202', 'abnormal embryo', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91886, 'HP:0034861', 'Reduced leukocyte arylsulfatase B activity', 'XPO:0141265', 'abnormal escape behavior', 0.5, 1.6758249395539064, 0.9153755894587495, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91887, 'HP:0034861', 'Reduced leukocyte arylsulfatase B activity', 'XPO:0100344', 'abnormal portion of organism substance', 0.47058823529411764, 1.6758249395539064, 0.8880447629295182, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91888, 'HP:0034861', 'Reduced leukocyte arylsulfatase B activity', 'XPO:0116494', 'absent biological process', 0.47058823529411764, 1.6758249395539064, 0.8880447629295182, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91889, 'HP:0034861', 'Reduced leukocyte arylsulfatase B activity', 'XPO:0100573', 'abnormal extraembryonic structure', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91890, 'HP:0034861', 'Reduced leukocyte arylsulfatase B activity', 'XPO:0141315', 'abnormal anatomical region', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91891, 'HP:0034861', 'Reduced leukocyte arylsulfatase B activity', 'XPO:0141770', 'abnormal urate homeostasis', 0.5, 1.6758249395539064, 0.9153755894587495, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91892, 'HP:0034861', 'Reduced leukocyte arylsulfatase B activity', 'XPO:0141771', 'abnormal urea homeostasis', 0.5, 1.6758249395539064, 0.9153755894587495, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91893, 'HP:0034861', 'Reduced leukocyte arylsulfatase B activity', 'XPO:0116434', 'abnormal biological process', 0.47058823529411764, 1.6758249395539064, 0.8880447629295182, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91894, 'HP:0034861', 'Reduced leukocyte arylsulfatase B activity', 'XPO:0100423', 'abnormal process', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91895, 'HP:0034861', 'Reduced leukocyte arylsulfatase B activity', 'XPO:0141267', 'abnormal resting posture', 0.5, 1.6758249395539064, 0.9153755894587495, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91896, 'HP:0034861', 'Reduced leukocyte arylsulfatase B activity', 'XPO:0141745', 'abnormal creatinine homeostasis', 0.5, 1.6758249395539064, 0.9153755894587495, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91897, 'HP:0034861', 'Reduced leukocyte arylsulfatase B activity', 'XPO:0115505', 'dead whole organism', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91898, 'HP:0034861', 'Reduced leukocyte arylsulfatase B activity', 'XPO:0100728', 'abnormal cell condensation', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91899, 'HP:0034861', 'Reduced leukocyte arylsulfatase B activity', 'XPO:0101569', 'abnormal activin-induced ectoderm', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91900, 'HP:0034861', 'Reduced leukocyte arylsulfatase B activity', 'XPO:0131729', 'abnormal regulation of growth rate', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91901, 'HP:0034861', 'Reduced leukocyte arylsulfatase B activity', 'XPO:0141271', 'increased surface breathing', 0.47058823529411764, 1.6758249395539064, 0.8880447629295182, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91902, 'HP:0034861', 'Reduced leukocyte arylsulfatase B activity', 'XPO:0141748', 'abnormal gas homeostasis', 0.5, 1.6758249395539064, 0.9153755894587495, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91903, 'HP:0034861', 'Reduced leukocyte arylsulfatase B activity', 'XPO:0141263', 'abnormal visually guided collision avoidance behavior', 0.5, 1.6758249395539064, 0.9153755894587495, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91904, 'HP:0034861', 'Reduced leukocyte arylsulfatase B activity', 'XPO:0100239', 'abnormal acellular anatomical structure', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91905, 'HP:0034861', 'Reduced leukocyte arylsulfatase B activity', 'XPO:0131723', 'abnormal pathway-restricted SMAD protein phosphorylation', 0.5, 1.6758249395539064, 0.9153755894587495, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91906, 'HP:0034861', 'Reduced leukocyte arylsulfatase B activity', 'XPO:0100062', 'abnormal anatomical space', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91907, 'HP:0034861', 'Reduced leukocyte arylsulfatase B activity', 'XPO:0141266', 'abnormal surface breathing', 0.5, 1.6758249395539064, 0.9153755894587495, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91908, 'HP:0034861', 'Reduced leukocyte arylsulfatase B activity', 'XPO:0141738', 'abnormal carbon dioxide homeostasis', 0.5, 1.6758249395539064, 0.9153755894587495, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91909, 'HP:0034861', 'Reduced leukocyte arylsulfatase B activity', 'XPO:0100969', 'abnormal disaggregated/reaggregated ectoderm treated with activin', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91910, 'HP:0034861', 'Reduced leukocyte arylsulfatase B activity', 'XPO:0107261', 'abnormal dorsal-ventral axis', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91911, 'HP:0034861', 'Reduced leukocyte arylsulfatase B activity', 'XPO:0107260', 'abnormal anterior-posterior axis', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91912, 'HP:0034861', 'Reduced leukocyte arylsulfatase B activity', 'XPO:0141272', 'absent surface breathing', 0.5, 1.6758249395539064, 0.9153755894587495, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91913, 'HP:0034861', 'Reduced leukocyte arylsulfatase B activity', 'XPO:0100006', 'abnormal anatomical structure', 0.47058823529411764, 1.6758249395539064, 0.8880447629295182, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91914, 'HP:0034861', 'Reduced leukocyte arylsulfatase B activity', 'XPO:00000000', 'Xenopus phenotype', 0.5333333333333333, 1.6758249395539064, 0.9453958435996092, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91915, 'HP:0034861', 'Reduced leukocyte arylsulfatase B activity', 'XPO:0141809', 'abnormal catalytic activity', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91916, 'HP:0034861', 'Reduced leukocyte arylsulfatase B activity', 'XPO:0133388', 'absent insulin receptor signaling pathway', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91917, 'HP:0034861', 'Reduced leukocyte arylsulfatase B activity', 'XPO:0141743', 'abnormal chemical homeostasis within a tissue', 0.5, 1.6758249395539064, 0.9153755894587495, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91918, 'HP:0034861', 'Reduced leukocyte arylsulfatase B activity', 'XPO:0131691', 'abnormal molecular function', 0.47058823529411764, 1.6758249395539064, 0.8880447629295182, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91919, 'HP:0034861', 'Reduced leukocyte arylsulfatase B activity', 'XPO:0107262', 'abnormal left-right axis', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91920, 'HP:0034861', 'Reduced leukocyte arylsulfatase B activity', 'XPO:0141264', 'abnormal schooling behavior', 0.5, 1.6758249395539064, 0.9153755894587495, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91921, 'HP:0034861', 'Reduced leukocyte arylsulfatase B activity', 'XPO:0107258', 'abnormal anatomical axis', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91922, 'HP:0034861', 'Reduced leukocyte arylsulfatase B activity', 'XPO:0128000', 'absent behavior', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91923, 'HP:0034861', 'Reduced leukocyte arylsulfatase B activity', 'XPO:0141776', 'abnormal metabolic process', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91924, 'HP:0034861', 'Reduced leukocyte arylsulfatase B activity', 'XPO:0115512', 'abnormally semi-erect whole organism', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91925, 'HP:0034861', 'Reduced leukocyte arylsulfatase B activity', 'XPO:0107270', 'abnormal proximal-distal axis', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91926, 'HP:0034861', 'Reduced leukocyte arylsulfatase B activity', 'XPO:0115509', 'abnormally semi-viable whole organism', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91927, 'HP:0034861', 'Reduced leukocyte arylsulfatase B activity', 'XPO:0141276', 'decreased surface breathing', 0.47058823529411764, 1.6758249395539064, 0.8880447629295182, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91928, 'HP:0034861', 'Reduced leukocyte arylsulfatase B activity', 'XPO:0101157', 'abnormal female organism', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91929, 'HP:0034861', 'Reduced leukocyte arylsulfatase B activity', 'XPO:0115508', 'abnormally peramorphic growth of whole organism', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91930, 'HP:0034861', 'Reduced leukocyte arylsulfatase B activity', 'XPO:0131469', 'abnormal heart process', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91931, 'HP:0034861', 'Reduced leukocyte arylsulfatase B activity', 'XPO:0141772', 'abnormal water homeostasis', 0.5, 1.6758249395539064, 0.9153755894587495, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91932, 'HP:0034861', 'Reduced leukocyte arylsulfatase B activity', 'XPO:0100084', 'abnormal anatomical group', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91933, 'HP:0034861', 'Reduced leukocyte arylsulfatase B activity', 'XPO:0131725', 'abnormal phosphorylation of RNA polymerase II C-terminal domain', 0.5, 1.6758249395539064, 0.9153755894587495, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91934, 'HP:0034861', 'Reduced leukocyte arylsulfatase B activity', 'XPO:0141754', 'abnormal homeostatic process', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91935, 'HP:0034861', 'Reduced leukocyte arylsulfatase B activity', 'XPO:0133403', 'abnormal developmental process', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91936, 'HP:0034861', 'Reduced leukocyte arylsulfatase B activity', 'XPO:0101109', 'abnormal egg cell-free extract', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91937, 'HP:0034861', 'Reduced leukocyte arylsulfatase B activity', 'XPO:0141499', 'abnormal tadpole', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91938, 'HP:0034861', 'Reduced leukocyte arylsulfatase B activity', 'XPO:0100481', 'abnormal anatomical line', 0.47058823529411764, 1.6758249395539064, 0.8880447629295182, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91939, 'HP:0034861', 'Reduced leukocyte arylsulfatase B activity', 'XPO:0141784', 'abnormal cellular hormone metabolic process', 0.5, 1.6758249395539064, 0.9153755894587495, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91940, 'HP:0034861', 'Reduced leukocyte arylsulfatase B activity', 'XPO:0101141', 'abnormal Keller explant', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91941, 'HP:0034861', 'Reduced leukocyte arylsulfatase B activity', 'XPO:0100081', 'abnormal anatomical entity in vitro', 0.47058823529411764, 1.6758249395539064, 0.8880447629295182, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91942, 'HP:0034861', 'Reduced leukocyte arylsulfatase B activity', 'XPO:0100258', 'abnormal organ part', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91943, 'HP:0034861', 'Reduced leukocyte arylsulfatase B activity', 'XPO:0100546', 'abnormal whole organism', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91944, 'HP:0034861', 'Reduced leukocyte arylsulfatase B activity', 'XPO:0141600', 'absent metamorphosis', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91945, 'HP:0034861', 'Reduced leukocyte arylsulfatase B activity', 'XPO:0100545', 'abnormal male organism', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91946, 'HP:0034861', 'Reduced leukocyte arylsulfatase B activity', 'XPO:0101110', 'abnormal cell-free extract', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91947, 'HP:0040107', 'Morphological abnormality of the posterior semicircular canal', 'XPO:0102835', 'abnormal vestibule morphology', 0.41025641025641024, 13.66854781257542, 2.3680391379800505, 'UPHENO:0019295', 'abnormal osseus labyrinth vestibule morphology'),
(91948, 'HP:0034239', 'Renal vein thrombosis', 'XPO:0101717', 'abnormal mesonephric sinus morphology', 0.41025641025641024, 7.667568053596582, 1.7736033787364254, 'UPHENO:0076779', 'abnormal kidney morphology'),
(91949, 'HP:0034261', 'Aplasia/Hypoplasia of facial bones', 'XPO:0102921', 'abnormal orbital region morphology', 0.40350877192982454, 8.103321529915524, 1.8082481353754303, 'UPHENO:0084457', 'abnormal facial skeleton morphology'),
(91950, 'HP:0020126', 'Prostate mass', 'XPO:0102397', 'abnormal male genitalia morphology', 0.40425531914893614, 9.217695178826904, 1.9303632576109295, 'UPHENO:0020950', 'abnormal reproductive system morphology'),
(91951, 'HP:0500097', 'Stool xenobiotic', 'XPO:0131723', 'abnormal pathway-restricted SMAD protein phosphorylation', 0.5333333333333333, 1.6758249395539064, 0.9453958435996092, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91952, 'HP:0500097', 'Stool xenobiotic', 'XPO:0101570', 'abnormal forelimb region', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91953, 'HP:0500097', 'Stool xenobiotic', 'XPO:0107263', 'abnormal anatomical side', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91954, 'HP:0500097', 'Stool xenobiotic', 'XPO:0141770', 'abnormal urate homeostasis', 0.5333333333333333, 1.6758249395539064, 0.9453958435996092, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91955, 'HP:0500097', 'Stool xenobiotic', 'XPO:0107261', 'abnormal dorsal-ventral axis', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91956, 'HP:0500097', 'Stool xenobiotic', 'XPO:0141958', 'absent cilium motility in left-right organizer', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91957, 'HP:0500097', 'Stool xenobiotic', 'XPO:0141271', 'increased surface breathing', 0.5, 1.6758249395539064, 0.9153755894587495, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91958, 'HP:0500097', 'Stool xenobiotic', 'XPO:0116429', 'abnormal behavior', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91959, 'HP:0500097', 'Stool xenobiotic', 'XPO:0141600', 'absent metamorphosis', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91960, 'HP:0500097', 'Stool xenobiotic', 'XPO:0100665', 'abnormal egg jelly', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91961, 'HP:0500097', 'Stool xenobiotic', 'XPO:0107273', 'abnormal basal region', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91962, 'HP:0500097', 'Stool xenobiotic', 'XPO:0141964', 'absent cilium motility in olfactory pit', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91963, 'HP:0500097', 'Stool xenobiotic', 'XPO:0100258', 'abnormal organ part', 0.47058823529411764, 1.6758249395539064, 0.8880447629295182, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91964, 'HP:0500097', 'Stool xenobiotic', 'XPO:0115508', 'abnormally peramorphic growth of whole organism', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91965, 'HP:0500097', 'Stool xenobiotic', 'XPO:0101141', 'abnormal Keller explant', 0.47058823529411764, 1.6758249395539064, 0.8880447629295182, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91966, 'HP:0500097', 'Stool xenobiotic', 'XPO:0100762', 'abnormal intersomitic region', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91967, 'HP:0500097', 'Stool xenobiotic', 'XPO:0101347', 'abnormal hindlimb region', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91968, 'HP:0500097', 'Stool xenobiotic', 'XPO:0116494', 'absent biological process', 0.5, 1.6758249395539064, 0.9153755894587495, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91969, 'HP:0500097', 'Stool xenobiotic', 'XPO:0141738', 'abnormal carbon dioxide homeostasis', 0.5333333333333333, 1.6758249395539064, 0.9453958435996092, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91970, 'HP:0500097', 'Stool xenobiotic', 'XPO:0141264', 'abnormal schooling behavior', 0.5333333333333333, 1.6758249395539064, 0.9453958435996092, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91971, 'HP:0500097', 'Stool xenobiotic', 'XPO:0131691', 'abnormal molecular function', 0.5, 1.6758249395539064, 0.9153755894587495, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91972, 'HP:0500097', 'Stool xenobiotic', 'XPO:0107271', 'abnormal apical region', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91973, 'HP:0500097', 'Stool xenobiotic', 'XPO:00000000', 'Xenopus phenotype', 0.5714285714285714, 1.6758249395539064, 0.9785776674202517, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91974, 'HP:0500097', 'Stool xenobiotic', 'XPO:0116433', 'abnormal axis specification', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91975, 'HP:0500097', 'Stool xenobiotic', 'XPO:0141265', 'abnormal escape behavior', 0.5333333333333333, 1.6758249395539064, 0.9453958435996092, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91976, 'HP:0500097', 'Stool xenobiotic', 'XPO:0115505', 'dead whole organism', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91977, 'HP:0500097', 'Stool xenobiotic', 'XPO:0100003', 'abnormal organism subdivision', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91978, 'HP:0500097', 'Stool xenobiotic', 'XPO:0141960', 'absent cilium motility in brain', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91979, 'HP:0500097', 'Stool xenobiotic', 'XPO:0100014', 'abnormal tissue', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91980, 'HP:0500097', 'Stool xenobiotic', 'XPO:0131730', 'abnormal regulation of protein folding', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91981, 'HP:0500097', 'Stool xenobiotic', 'XPO:0100062', 'abnormal anatomical space', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91982, 'HP:0500097', 'Stool xenobiotic', 'XPO:0100573', 'abnormal extraembryonic structure', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91983, 'HP:0500097', 'Stool xenobiotic', 'XPO:0100545', 'abnormal male organism', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91984, 'HP:0500097', 'Stool xenobiotic', 'XPO:0100546', 'abnormal whole organism', 0.47058823529411764, 1.6758249395539064, 0.8880447629295182, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91985, 'HP:0500097', 'Stool xenobiotic', 'XPO:0100728', 'abnormal cell condensation', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91986, 'HP:0500097', 'Stool xenobiotic', 'XPO:0116434', 'abnormal biological process', 0.5, 1.6758249395539064, 0.9153755894587495, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91987, 'HP:0500097', 'Stool xenobiotic', 'XPO:0115512', 'abnormally semi-erect whole organism', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91988, 'HP:0500097', 'Stool xenobiotic', 'XPO:0100004', 'abnormal cell', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91989, 'HP:0500097', 'Stool xenobiotic', 'XPO:0107272', 'abnormal axial region', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91990, 'HP:0500097', 'Stool xenobiotic', 'XPO:0141263', 'abnormal visually guided collision avoidance behavior', 0.5333333333333333, 1.6758249395539064, 0.9453958435996092, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91991, 'HP:0500097', 'Stool xenobiotic', 'XPO:0100202', 'abnormal embryo', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91992, 'HP:0500097', 'Stool xenobiotic', 'XPO:0141784', 'abnormal cellular hormone metabolic process', 0.5333333333333333, 1.6758249395539064, 0.9453958435996092, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91993, 'HP:0500097', 'Stool xenobiotic', 'XPO:0100104', 'abnormal embryonic structure', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91994, 'HP:0500097', 'Stool xenobiotic', 'XPO:0100277', 'abnormal blastocoel', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91995, 'HP:0500097', 'Stool xenobiotic', 'XPO:0100006', 'abnormal anatomical structure', 0.5, 1.6758249395539064, 0.9153755894587495, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91996, 'HP:0500097', 'Stool xenobiotic', 'XPO:0107270', 'abnormal proximal-distal axis', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91997, 'HP:0500097', 'Stool xenobiotic', 'XPO:0100009', 'abnormal multi-tissue structure', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91998, 'HP:0500097', 'Stool xenobiotic', 'XPO:0141959', 'absent cilium motility in floor plate', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(91999, 'HP:0500097', 'Stool xenobiotic', 'XPO:0101157', 'abnormal female organism', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92000, 'HP:0500097', 'Stool xenobiotic', 'XPO:0100070', 'abnormal anatomical system', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92001, 'HP:0500097', 'Stool xenobiotic', 'XPO:0133403', 'abnormal developmental process', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92002, 'HP:0500097', 'Stool xenobiotic', 'XPO:0100295', 'abnormal extracellular matrix', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92003, 'HP:0500097', 'Stool xenobiotic', 'XPO:0141745', 'abnormal creatinine homeostasis', 0.5333333333333333, 1.6758249395539064, 0.9453958435996092, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92004, 'HP:0500097', 'Stool xenobiotic', 'XPO:0101109', 'abnormal egg cell-free extract', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92005, 'HP:0500097', 'Stool xenobiotic', 'XPO:0141272', 'absent surface breathing', 0.5333333333333333, 1.6758249395539064, 0.9453958435996092, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92006, 'HP:0500097', 'Stool xenobiotic', 'XPO:0100643', 'abnormal thoracic region', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92007, 'HP:0500097', 'Stool xenobiotic', 'XPO:0131740', 'abnormal detection of nodal flow', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92008, 'HP:0500097', 'Stool xenobiotic', 'XPO:0141754', 'abnormal homeostatic process', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92009, 'HP:0500097', 'Stool xenobiotic', 'XPO:0101200', 'abnormal joint region', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92010, 'HP:0500097', 'Stool xenobiotic', 'XPO:0100423', 'abnormal process', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92011, 'HP:0500097', 'Stool xenobiotic', 'XPO:0131744', 'abnormal apical constriction', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92012, 'HP:0500097', 'Stool xenobiotic', 'XPO:0100010', 'abnormal multicellular anatomical structure', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92013, 'HP:0500097', 'Stool xenobiotic', 'XPO:0131469', 'abnormal heart process', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92014, 'HP:0500097', 'Stool xenobiotic', 'XPO:0141276', 'decreased surface breathing', 0.5, 1.6758249395539064, 0.9153755894587495, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92015, 'HP:0500097', 'Stool xenobiotic', 'XPO:0107259', 'abnormal animal-vegetal axis', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92016, 'HP:0500097', 'Stool xenobiotic', 'XPO:0141315', 'abnormal anatomical region', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92017, 'HP:0500097', 'Stool xenobiotic', 'XPO:0100344', 'abnormal portion of organism substance', 0.5, 1.6758249395539064, 0.9153755894587495, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92018, 'HP:0500097', 'Stool xenobiotic', 'XPO:0107278', 'abnormal medial region', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92019, 'HP:0500097', 'Stool xenobiotic', 'XPO:0141771', 'abnormal urea homeostasis', 0.5333333333333333, 1.6758249395539064, 0.9453958435996092, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92020, 'HP:0500097', 'Stool xenobiotic', 'XPO:0107276', 'abnormal dorsal region', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92021, 'HP:0500097', 'Stool xenobiotic', 'XPO:0115509', 'abnormally semi-viable whole organism', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92022, 'HP:0500097', 'Stool xenobiotic', 'XPO:0131719', 'abnormal activation of meiosis', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92023, 'HP:0500097', 'Stool xenobiotic', 'XPO:0131722', 'abnormal determination of left/right symmetry', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92024, 'HP:0500097', 'Stool xenobiotic', 'XPO:0131729', 'abnormal regulation of growth rate', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92025, 'HP:0500097', 'Stool xenobiotic', 'XPO:0141975', 'abnormal cilium motility', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92026, 'HP:0500097', 'Stool xenobiotic', 'XPO:0131703', 'abnormal cell division', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92027, 'HP:0500097', 'Stool xenobiotic', 'XPO:0141267', 'abnormal resting posture', 0.5333333333333333, 1.6758249395539064, 0.9453958435996092, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92028, 'HP:0500097', 'Stool xenobiotic', 'XPO:0101110', 'abnormal cell-free extract', 0.47058823529411764, 1.6758249395539064, 0.8880447629295182, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92029, 'HP:0500097', 'Stool xenobiotic', 'XPO:0141266', 'abnormal surface breathing', 0.5333333333333333, 1.6758249395539064, 0.9453958435996092, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92030, 'HP:0500097', 'Stool xenobiotic', 'XPO:0131725', 'abnormal phosphorylation of RNA polymerase II C-terminal domain', 0.5333333333333333, 1.6758249395539064, 0.9453958435996092, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92031, 'HP:0500097', 'Stool xenobiotic', 'XPO:0133340', 'abnormal cell adhesion', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92032, 'HP:0500097', 'Stool xenobiotic', 'XPO:0141499', 'abnormal tadpole', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92033, 'HP:0500097', 'Stool xenobiotic', 'XPO:0100081', 'abnormal anatomical entity in vitro', 0.5, 1.6758249395539064, 0.9153755894587495, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92034, 'HP:0500097', 'Stool xenobiotic', 'XPO:0141724', 'abnormal prevention of polyspermy', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92035, 'HP:0500097', 'Stool xenobiotic', 'XPO:0141962', 'absent cilium motility in pronephric kidney', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92036, 'HP:0500097', 'Stool xenobiotic', 'XPO:0141743', 'abnormal chemical homeostasis within a tissue', 0.5333333333333333, 1.6758249395539064, 0.9453958435996092, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92037, 'HP:0500097', 'Stool xenobiotic', 'XPO:0107258', 'abnormal anatomical axis', 0.47058823529411764, 1.6758249395539064, 0.8880447629295182, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92038, 'HP:0500097', 'Stool xenobiotic', 'XPO:0100969', 'abnormal disaggregated/reaggregated ectoderm treated with activin', 0.47058823529411764, 1.6758249395539064, 0.8880447629295182, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92039, 'HP:0500097', 'Stool xenobiotic', 'XPO:0141809', 'abnormal catalytic activity', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92040, 'HP:0500097', 'Stool xenobiotic', 'XPO:0101411', 'abnormal marginal zone (sensu neural)', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92041, 'HP:0500097', 'Stool xenobiotic', 'XPO:0100028', 'abnormal anatomical cluster', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92042, 'HP:0500097', 'Stool xenobiotic', 'XPO:0128000', 'absent behavior', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92043, 'HP:0500097', 'Stool xenobiotic', 'XPO:0101569', 'abnormal activin-induced ectoderm', 0.47058823529411764, 1.6758249395539064, 0.8880447629295182, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92044, 'HP:0500097', 'Stool xenobiotic', 'XPO:0133388', 'absent insulin receptor signaling pathway', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92045, 'HP:0500097', 'Stool xenobiotic', 'XPO:0107260', 'abnormal anterior-posterior axis', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92046, 'HP:0500097', 'Stool xenobiotic', 'XPO:0133401', 'absent determination of left/right symmetry in lateral plate mesoderm', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92047, 'HP:0500097', 'Stool xenobiotic', 'XPO:0100481', 'abnormal anatomical line', 0.5, 1.6758249395539064, 0.9153755894587495, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92048, 'HP:0500097', 'Stool xenobiotic', 'XPO:0141748', 'abnormal gas homeostasis', 0.5333333333333333, 1.6758249395539064, 0.9453958435996092, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92049, 'HP:0500097', 'Stool xenobiotic', 'XPO:0100239', 'abnormal acellular anatomical structure', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92050, 'HP:0500097', 'Stool xenobiotic', 'XPO:0141776', 'abnormal metabolic process', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92051, 'HP:0500097', 'Stool xenobiotic', 'XPO:0141772', 'abnormal water homeostasis', 0.5333333333333333, 1.6758249395539064, 0.9453958435996092, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92052, 'HP:0500097', 'Stool xenobiotic', 'XPO:0107262', 'abnormal left-right axis', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92053, 'HP:0500097', 'Stool xenobiotic', 'XPO:0100084', 'abnormal anatomical group', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92054, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0107258', 'abnormal anatomical axis', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92055, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0100289', 'abnormal chondroblast', 0.4166666666666667, 4.8755453832354885, 1.4252990012677296, 'UPHENO:0086172', 'abnormal cell'),
(92056, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0101004', 'abnormal acid secreting cell', 0.4166666666666667, 4.8755453832354885, 1.4252990012677296, 'UPHENO:0086172', 'abnormal cell'),
(92057, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0140395', 'abnormally necrotic antero-dorsal region', 0.42857142857142855, 3.008048030199787, 1.1354133350961642, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(92058, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102800', 'abnormal circulating cell morphology', 0.42424242424242425, 6.121988824155609, 1.6115853622891974, 'UPHENO:0084928', 'abnormal cell morphology'),
(92059, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102773', 'abnormal Keller explant morphology', 0.48, 3.008048030199787, 1.2016085279723583, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(92060, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0107351', 'abnormal anterior side morphology', 0.41379310344827586, 3.008048030199787, 1.1156655097912829, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(92061, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0141165', 'abnormally necrotic ventral region', 0.42857142857142855, 3.008048030199787, 1.1354133350961642, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(92062, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102745', 'abnormal stage IV oocyte morphology', 0.4375, 6.121988824155609, 1.6365726719483247, 'UPHENO:0084928', 'abnormal cell morphology'),
(92063, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0140752', 'abnormally necrotic melanoblast', 0.4375, 6.121988824155609, 1.6365726719483247, 'UPHENO:0084928', 'abnormal cell morphology'),
(92064, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0139839', 'abnormally necrotic progenitor cell', 0.4375, 6.121988824155609, 1.6365726719483247, 'UPHENO:0084928', 'abnormal cell morphology'),
(92065, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102135', 'abnormal blastomere D2 morphology', 0.4117647058823529, 6.121988824155609, 1.5877087036334738, 'UPHENO:0084928', 'abnormal cell morphology'),
(92066, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0103219', 'abnormal hemangioblast morphology', 0.42424242424242425, 6.121988824155609, 1.6115853622891974, 'UPHENO:0084928', 'abnormal cell morphology'),
(92067, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0139886', 'abnormally necrotic process', 0.41379310344827586, 3.008048030199787, 1.1156655097912829, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(92068, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102742', 'abnormal cell-free extract morphology', 0.48, 3.008048030199787, 1.2016085279723583, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(92069, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0141503', 'abnormal lymphoblast morphology', 0.42424242424242425, 6.121988824155609, 1.6115853622891974, 'UPHENO:0084928', 'abnormal cell morphology'),
(92070, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0100754', 'abnormal electrically active cell', 0.4166666666666667, 4.8755453832354885, 1.4252990012677296, 'UPHENO:0086172', 'abnormal cell'),
(92071, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0101917', 'abnormal progenitor cell morphology', 0.5, 6.121988824155609, 1.7495697791393758, 'UPHENO:0084928', 'abnormal cell morphology'),
(92072, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0140284', 'abnormally necrotic dorsal region', 0.41379310344827586, 3.008048030199787, 1.1156655097912829, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(92073, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0100791', 'abnormal multiciliated cell precursor', 0.4166666666666667, 4.8755453832354885, 1.4252990012677296, 'UPHENO:0086172', 'abnormal cell'),
(92074, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102539', 'abnormal cytoplasm morphology', 0.4482758620689655, 4.8755453832354885, 1.478373873459029, 'UPHENO:0086172', 'abnormal cell'),
(92075, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0140068', 'abnormally necrotic myoblast', 0.4375, 6.121988824155609, 1.6365726719483247, 'UPHENO:0084928', 'abnormal cell morphology'),
(92076, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0100108', 'abnormal cell part', 0.4166666666666667, 4.8755453832354885, 1.4252990012677296, 'UPHENO:0086172', 'abnormal cell'),
(92077, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102179', 'abnormal blastomere V2 morphology', 0.4117647058823529, 6.121988824155609, 1.5877087036334738, 'UPHENO:0084928', 'abnormal cell morphology'),
(92078, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0139763', 'abnormally necrotic anatomical group', 0.41379310344827586, 3.008048030199787, 1.1156655097912829, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(92079, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0101871', 'abnormal acellular anatomical structure morphology', 0.46153846153846156, 3.008048030199787, 1.178274102275107, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(92080, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0128091', 'decreased size of the anatomical region', 0.41379310344827586, 3.008048030199787, 1.1156655097912829, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(92081, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0142064', 'abnormal desmosome morphology', 0.4482758620689655, 4.8755453832354885, 1.478373873459029, 'UPHENO:0086172', 'abnormal cell'),
(92082, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0107346', 'abnormal animal-vegetal axis morphology', 0.4444444444444444, 3.008048030199787, 1.1562483451423184, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(92083, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0101736', 'abnormal embryonic structure morphology', 0.42857142857142855, 3.008048030199787, 1.1354133350961642, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(92084, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102258', 'abnormal primordial germ cell morphology', 0.4666666666666667, 6.121988824155609, 1.6902449875504095, 'UPHENO:0084928', 'abnormal cell morphology'),
(92085, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0107356', 'abnormal right side morphology', 0.41379310344827586, 3.008048030199787, 1.1156655097912829, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(92086, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0107355', 'abnormal left side morphology', 0.41379310344827586, 3.008048030199787, 1.1156655097912829, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(92087, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0129571', 'increased size of the anatomical region', 0.41379310344827586, 3.008048030199787, 1.1156655097912829, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(92088, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0141146', 'abnormally necrotic oxygen accumulating cell', 0.4375, 6.121988824155609, 1.6365726719483247, 'UPHENO:0084928', 'abnormal cell morphology'),
(92089, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0101660', 'abnormal anatomical cluster morphology', 0.42857142857142855, 3.008048030199787, 1.1354133350961642, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(92090, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0107350', 'abnormal anatomical side morphology', 0.4444444444444444, 3.008048030199787, 1.1562483451423184, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(92091, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102789', 'abnormal female organism morphology', 0.4444444444444444, 3.008048030199787, 1.1562483451423184, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(92092, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102739', 'abnormal erythroid cell morphology', 0.42424242424242425, 6.121988824155609, 1.6115853622891974, 'UPHENO:0084928', 'abnormal cell morphology'),
(92093, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0100004', 'abnormal cell', 0.43478260869565216, 4.8755453832354885, 1.4559540997356917, 'UPHENO:0086172', 'abnormal cell'),
(92094, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0140381', 'abnormally necrotic ciliated cell', 0.4375, 6.121988824155609, 1.6365726719483247, 'UPHENO:0084928', 'abnormal cell morphology'),
(92095, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0141316', 'abnormal anatomical region morphology', 0.48, 3.008048030199787, 1.2016085279723583, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(92096, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102741', 'abnormal egg cell-free extract morphology', 0.4444444444444444, 3.008048030199787, 1.1562483451423184, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(92097, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102764', 'abnormal apoptotic cell morphology', 0.5, 6.121988824155609, 1.7495697791393758, 'UPHENO:0084928', 'abnormal cell morphology'),
(92098, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0140179', 'abnormally necrotic postero-dorsal region', 0.42857142857142855, 3.008048030199787, 1.1354133350961642, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(92099, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0107399', 'abnormal filopodium morphology', 0.4482758620689655, 4.8755453832354885, 1.478373873459029, 'UPHENO:0086172', 'abnormal cell'),
(92100, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0101448', 'abnormal myelin accumulating cell', 0.4166666666666667, 4.8755453832354885, 1.4252990012677296, 'UPHENO:0086172', 'abnormal cell'),
(92101, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0139841', 'abnormally necrotic anatomical region', 0.4444444444444444, 3.008048030199787, 1.1562483451423184, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(92102, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0129487', 'increased size of the anatomical structure', 0.4444444444444444, 3.008048030199787, 1.1562483451423184, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(92103, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0101927', 'abnormal extracellular matrix morphology', 0.42857142857142855, 3.008048030199787, 1.1354133350961642, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(92104, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102873', 'abnormal nucleate erythrocyte morphology', 0.5, 6.121988824155609, 1.7495697791393758, 'UPHENO:0084928', 'abnormal cell morphology'),
(92105, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102520', 'abnormal microtubule morphology', 0.4482758620689655, 4.8755453832354885, 1.478373873459029, 'UPHENO:0086172', 'abnormal cell'),
(92106, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0101237', 'abnormal mucus secreting cell', 0.4166666666666667, 4.8755453832354885, 1.4252990012677296, 'UPHENO:0086172', 'abnormal cell'),
(92107, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0141065', 'abnormally necrotic paracrine cell', 0.4375, 6.121988824155609, 1.6365726719483247, 'UPHENO:0084928', 'abnormal cell morphology'),
(92108, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0128102', 'decreased size of the portion of organism substance', 0.4444444444444444, 3.008048030199787, 1.1562483451423184, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(92109, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102994', 'abnormal vegetal cortex morphology', 0.40625, 4.8755453832354885, 1.4073699982376409, 'UPHENO:0086172', 'abnormal cell'),
(92110, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0107352', 'abnormal posterior side morphology', 0.41379310344827586, 3.008048030199787, 1.1156655097912829, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(92111, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102704', 'abnormal mitochondrial cloud morphology', 0.41935483870967744, 4.8755453832354885, 1.4298893480995063, 'UPHENO:0086172', 'abnormal cell'),
(92112, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0103043', 'abnormal marginal zone (sensu neural) morphology', 0.4444444444444444, 3.008048030199787, 1.1562483451423184, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(92113, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0140278', 'abnormally necrotic Merkel cell', 0.4375, 6.121988824155609, 1.6365726719483247, 'UPHENO:0084928', 'abnormal cell morphology'),
(92114, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0101835', 'abnormal endocrine cell morphology', 0.42424242424242425, 6.121988824155609, 1.6115853622891974, 'UPHENO:0084928', 'abnormal cell morphology'),
(92115, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102336', 'abnormal Merkel cell morphology', 0.5, 6.121988824155609, 1.7495697791393758, 'UPHENO:0084928', 'abnormal cell morphology'),
(92116, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0140899', 'abnormally necrotic mucus secreting cell', 0.4375, 6.121988824155609, 1.6365726719483247, 'UPHENO:0084928', 'abnormal cell morphology'),
(92117, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0100802', 'abnormal exocrine cell', 0.4166666666666667, 4.8755453832354885, 1.4252990012677296, 'UPHENO:0086172', 'abnormal cell'),
(92118, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102852', 'abnormal centriole morphology', 0.43333333333333335, 4.8755453832354885, 1.453525484033692, 'UPHENO:0086172', 'abnormal cell'),
(92119, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0139923', 'abnormally necrotic acellular anatomical structure', 0.41379310344827586, 3.008048030199787, 1.1156655097912829, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(92120, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0101940', 'abnormal early embryonic cell morphology', 0.4666666666666667, 6.121988824155609, 1.6902449875504095, 'UPHENO:0084928', 'abnormal cell morphology'),
(92121, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0103005', 'abnormal oxygen accumulating cell morphology', 0.5, 6.121988824155609, 1.7495697791393758, 'UPHENO:0084928', 'abnormal cell morphology'),
(92122, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102519', 'abnormal right-dorsal blastomere morphology', 0.4117647058823529, 6.121988824155609, 1.5877087036334738, 'UPHENO:0084928', 'abnormal cell morphology'),
(92123, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102024', 'abnormal cilium morphology', 0.43333333333333335, 4.8755453832354885, 1.453525484033692, 'UPHENO:0086172', 'abnormal cell'),
(92124, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0101241', 'abnormal nucleate erythrocyte', 0.4166666666666667, 4.8755453832354885, 1.4252990012677296, 'UPHENO:0086172', 'abnormal cell'),
(92125, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0100481', 'abnormal anatomical line', 0.42857142857142855, 1.7901636446558942, 0.8759069531444602, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92126, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0129551', 'increased size of the cell part', 0.40625, 4.8755453832354885, 1.4073699982376409, 'UPHENO:0086172', 'abnormal cell'),
(92127, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0100337', 'abnormal zygote', 0.4166666666666667, 4.8755453832354885, 1.4252990012677296, 'UPHENO:0086172', 'abnormal cell'),
(92128, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102958', 'abnormal cementoblast morphology', 0.5, 6.121988824155609, 1.7495697791393758, 'UPHENO:0084928', 'abnormal cell morphology'),
(92129, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102794', 'abnormal stromal cell morphology', 0.4375, 6.121988824155609, 1.6365726719483247, 'UPHENO:0084928', 'abnormal cell morphology'),
(92130, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0139713', 'abnormally necrotic multicellular anatomical structure', 0.41379310344827586, 3.008048030199787, 1.1156655097912829, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(92131, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0101646', 'abnormal tissue morphology', 0.42857142857142855, 3.008048030199787, 1.1354133350961642, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(92132, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102177', 'abnormal male organism morphology', 0.4444444444444444, 3.008048030199787, 1.1562483451423184, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(92133, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0140647', 'abnormally necrotic nucleate erythrocyte', 0.4375, 6.121988824155609, 1.6365726719483247, 'UPHENO:0084928', 'abnormal cell morphology'),
(92134, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0101297', 'abnormal barrier cell', 0.4166666666666667, 4.8755453832354885, 1.4252990012677296, 'UPHENO:0086172', 'abnormal cell'),
(92135, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102872', 'abnormal ciliated non-epidermal cell morphology', 0.4666666666666667, 6.121988824155609, 1.6902449875504095, 'UPHENO:0084928', 'abnormal cell morphology'),
(92136, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0141091', 'abnormally necrotic posterior region', 0.42857142857142855, 3.008048030199787, 1.1354133350961642, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(92137, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0140589', 'abnormally necrotic keratin accumulating cell', 0.4375, 6.121988824155609, 1.6365726719483247, 'UPHENO:0084928', 'abnormal cell morphology'),
(92138, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0101326', 'abnormal cementoblast', 0.4166666666666667, 4.8755453832354885, 1.4252990012677296, 'UPHENO:0086172', 'abnormal cell'),
(92139, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0101694', 'abnormal anatomical space morphology', 0.48, 3.008048030199787, 1.2016085279723583, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(92140, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0100969', 'abnormal disaggregated/reaggregated ectoderm treated with activin', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92141, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0101373', 'abnormal oxygen accumulating cell', 0.4166666666666667, 4.8755453832354885, 1.4252990012677296, 'UPHENO:0086172', 'abnormal cell'),
(92142, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102423', 'abnormal multiciliated cell precursor morphology', 0.5, 6.121988824155609, 1.7495697791393758, 'UPHENO:0084928', 'abnormal cell morphology'),
(92143, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102275', 'abnormal thoracic region morphology', 0.4444444444444444, 3.008048030199787, 1.1562483451423184, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(92144, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0103130', 'abnormal stage II oocyte morphology', 0.4375, 6.121988824155609, 1.6365726719483247, 'UPHENO:0084928', 'abnormal cell morphology'),
(92145, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0115510', 'abnormal degeneration of whole organism', 0.46153846153846156, 3.008048030199787, 1.178274102275107, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(92146, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102270', 'abnormal polar body morphology', 0.45161290322580644, 6.121988824155609, 1.6627594974598268, 'UPHENO:0084928', 'abnormal cell morphology'),
(92147, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0133438', 'abnormal cilium morphology in the ciliated non-epidermal cell', 0.40625, 4.8755453832354885, 1.4073699982376409, 'UPHENO:0086172', 'abnormal cell'),
(92148, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102181', 'abnormal mitotic cell morphology', 0.5, 6.121988824155609, 1.7495697791393758, 'UPHENO:0084928', 'abnormal cell morphology'),
(92149, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102526', 'abnormal nucleus morphology', 0.4482758620689655, 4.8755453832354885, 1.478373873459029, 'UPHENO:0086172', 'abnormal cell'),
(92150, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0141334', 'increased pigmentation in the whole organism', 0.42857142857142855, 3.008048030199787, 1.1354133350961642, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(92151, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0140373', 'abnormally necrotic whole organism', 0.42857142857142855, 3.008048030199787, 1.1354133350961642, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(92152, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102113', 'abnormal anatomical line morphology', 0.5217391304347826, 3.008048030199787, 1.2527634906807021, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(92153, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0140052', 'abnormally necrotic organ part', 0.42857142857142855, 3.008048030199787, 1.1354133350961642, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(92154, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0101807', 'abnormal migrating neuroblast morphology', 0.42424242424242425, 6.121988824155609, 1.6115853622891974, 'UPHENO:0084928', 'abnormal cell morphology'),
(92155, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102069', 'abnormal proepicardium morphology', 0.4666666666666667, 6.121988824155609, 1.6902449875504095, 'UPHENO:0084928', 'abnormal cell morphology'),
(92156, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102474', 'abnormal left-dorsal blastomere morphology', 0.4117647058823529, 6.121988824155609, 1.5877087036334738, 'UPHENO:0084928', 'abnormal cell morphology'),
(92157, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0128502', 'decreased size of the anatomical line', 0.4444444444444444, 3.008048030199787, 1.1562483451423184, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(92158, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102808', 'abnormal non-ciliated epithelial cell morphology', 0.42424242424242425, 6.121988824155609, 1.6115853622891974, 'UPHENO:0084928', 'abnormal cell morphology'),
(92159, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0129517', 'increased size of the anatomical space', 0.41379310344827586, 3.008048030199787, 1.1156655097912829, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(92160, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0107353', 'abnormal dorsal side morphology', 0.41379310344827586, 3.008048030199787, 1.1156655097912829, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(92161, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0100006', 'abnormal anatomical structure', 0.42857142857142855, 1.7901636446558942, 0.8759069531444602, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92162, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0140471', 'abnormally necrotic multiciliated cell precursor', 0.4375, 6.121988824155609, 1.6365726719483247, 'UPHENO:0084928', 'abnormal cell morphology'),
(92163, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102205', 'abnormal extraembryonic structure morphology', 0.4444444444444444, 3.008048030199787, 1.1562483451423184, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(92164, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102636', 'abnormal acid secreting cell morphology', 0.5, 6.121988824155609, 1.7495697791393758, 'UPHENO:0084928', 'abnormal cell morphology'),
(92165, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0103021', 'abnormal wedge region morphology', 0.41935483870967744, 4.8755453832354885, 1.4298893480995063, 'UPHENO:0086172', 'abnormal cell'),
(92166, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0139759', 'abnormally necrotic germ cell', 0.4375, 6.121988824155609, 1.6365726719483247, 'UPHENO:0084928', 'abnormal cell morphology'),
(92167, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0142067', 'abnormally necrotic desmosome', 0.40625, 4.8755453832354885, 1.4073699982376409, 'UPHENO:0086172', 'abnormal cell'),
(92168, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0101641', 'abnormal multi-tissue structure morphology', 0.42857142857142855, 3.008048030199787, 1.1354133350961642, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(92169, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102434', 'abnormal exocrine cell morphology', 0.5, 6.121988824155609, 1.7495697791393758, 'UPHENO:0084928', 'abnormal cell morphology'),
(92170, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0101657', 'abnormal oocyte morphology', 0.4666666666666667, 6.121988824155609, 1.6902449875504095, 'UPHENO:0084928', 'abnormal cell morphology'),
(92171, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102347', 'abnormal ciliated cell morphology', 0.5, 6.121988824155609, 1.7495697791393758, 'UPHENO:0084928', 'abnormal cell morphology'),
(92172, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102147', 'abnormal somatic stem cell morphology', 0.4666666666666667, 6.121988824155609, 1.6902449875504095, 'UPHENO:0084928', 'abnormal cell morphology'),
(92173, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102588', 'abnormal centrosome morphology', 0.4482758620689655, 4.8755453832354885, 1.478373873459029, 'UPHENO:0086172', 'abnormal cell'),
(92174, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0141203', 'abnormally necrotic exocrine cell', 0.4375, 6.121988824155609, 1.6365726719483247, 'UPHENO:0084928', 'abnormal cell morphology'),
(92175, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0141285', 'abnormal cortical actin cytoskeleton morphology', 0.43333333333333335, 4.8755453832354885, 1.453525484033692, 'UPHENO:0086172', 'abnormal cell'),
(92176, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0140269', 'abnormally necrotic anatomical line', 0.48, 3.008048030199787, 1.2016085279723583, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(92177, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0100344', 'abnormal portion of organism substance', 0.42857142857142855, 1.7901636446558942, 0.8759069531444602, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92178, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0140167', 'abnormally necrotic medial region', 0.41379310344827586, 3.008048030199787, 1.1156655097912829, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(92179, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102386', 'abnormal electrically active cell morphology', 0.5, 6.121988824155609, 1.7495697791393758, 'UPHENO:0084928', 'abnormal cell morphology'),
(92180, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102601', 'abnormal disaggregated/reaggregated ectoderm treated with activin morphology', 0.48, 3.008048030199787, 1.2016085279723583, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(92181, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102165', 'abnormal melanoblast morphology', 0.5, 6.121988824155609, 1.7495697791393758, 'UPHENO:0084928', 'abnormal cell morphology'),
(92182, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102915', 'abnormal left-ventral blastomere morphology', 0.4117647058823529, 6.121988824155609, 1.5877087036334738, 'UPHENO:0084928', 'abnormal cell morphology'),
(92183, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0107349', 'abnormal left-right axis morphology', 0.4444444444444444, 3.008048030199787, 1.1562483451423184, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(92184, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0128071', 'decreased size of the cell part', 0.40625, 4.8755453832354885, 1.4073699982376409, 'UPHENO:0086172', 'abnormal cell'),
(92185, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102394', 'abnormal intersomitic region morphology', 0.41379310344827586, 3.008048030199787, 1.1156655097912829, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(92186, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0101890', 'abnormal organ part morphology', 0.48, 3.008048030199787, 1.2016085279723583, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(92187, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102360', 'abnormal cell condensation morphology', 0.46153846153846156, 3.008048030199787, 1.178274102275107, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(92188, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0103112', 'abnormal stage V oocyte morphology', 0.4375, 6.121988824155609, 1.6365726719483247, 'UPHENO:0084928', 'abnormal cell morphology'),
(92189, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0140868', 'abnormally necrotic chondroblast', 0.4375, 6.121988824155609, 1.6365726719483247, 'UPHENO:0084928', 'abnormal cell morphology'),
(92190, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0107371', 'abnormal migrating myoblast morphology', 0.4666666666666667, 6.121988824155609, 1.6902449875504095, 'UPHENO:0084928', 'abnormal cell morphology'),
(92191, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102285', 'abnormal myoblast morphology', 0.5, 6.121988824155609, 1.7495697791393758, 'UPHENO:0084928', 'abnormal cell morphology'),
(92192, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0107345', 'abnormal anatomical axis morphology', 0.48, 3.008048030199787, 1.2016085279723583, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(92193, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0101658', 'abnormal germ cell morphology', 0.5, 6.121988824155609, 1.7495697791393758, 'UPHENO:0084928', 'abnormal cell morphology'),
(92194, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0101569', 'abnormal activin-induced ectoderm', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92195, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0140955', 'abnormally necrotic ventro-lateral region', 0.42857142857142855, 3.008048030199787, 1.1354133350961642, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(92196, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0101939', 'abnormal blastomere morphology', 0.4375, 6.121988824155609, 1.6365726719483247, 'UPHENO:0084928', 'abnormal cell morphology'),
(92197, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102934', 'abnormal subcortical cytoplasm morphology', 0.41935483870967744, 4.8755453832354885, 1.4298893480995063, 'UPHENO:0086172', 'abnormal cell'),
(92198, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0139717', 'abnormally necrotic cell', 0.4827586206896552, 6.121988824155609, 1.7191401573539156, 'UPHENO:0084928', 'abnormal cell morphology'),
(92199, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0101141', 'abnormal Keller explant', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92200, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0141299', 'abnormal actin filament morphology', 0.43333333333333335, 4.8755453832354885, 1.453525484033692, 'UPHENO:0086172', 'abnormal cell'),
(92201, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0133436', 'abnormal cilium morphology in the multiciliated cell', 0.40625, 4.8755453832354885, 1.4073699982376409, 'UPHENO:0086172', 'abnormal cell'),
(92202, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0101636', 'abnormal cell morphology', 0.5384615384615384, 6.121988824155609, 1.8156143645331664, 'UPHENO:0084928', 'abnormal cell morphology'),
(92203, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0128007', 'decreased size of the anatomical structure', 0.4444444444444444, 3.008048030199787, 1.1562483451423184, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(92204, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0140533', 'abnormally necrotic myelin accumulating cell', 0.4375, 6.121988824155609, 1.6365726719483247, 'UPHENO:0084928', 'abnormal cell morphology'),
(92205, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0100715', 'abnormal ciliated cell', 0.4166666666666667, 4.8755453832354885, 1.4252990012677296, 'UPHENO:0086172', 'abnormal cell'),
(92206, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0107348', 'abnormal dorsal-ventral axis morphology', 0.4444444444444444, 3.008048030199787, 1.1562483451423184, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(92207, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0141048', 'abnormally necrotic mitotic cell', 0.4375, 6.121988824155609, 1.6365726719483247, 'UPHENO:0084928', 'abnormal cell morphology'),
(92208, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0140364', 'abnormally necrotic anterior region', 0.42857142857142855, 3.008048030199787, 1.1354133350961642, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(92209, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0141189', 'abnormally necrotic antero-ventral region', 0.42857142857142855, 3.008048030199787, 1.1354133350961642, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(92210, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102693', 'abnormal plasma membrane morphology', 0.4482758620689655, 4.8755453832354885, 1.478373873459029, 'UPHENO:0086172', 'abnormal cell'),
(92211, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0101716', 'abnormal anatomical group morphology', 0.46153846153846156, 3.008048030199787, 1.178274102275107, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(92212, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0103927', 'decreased pigmentation in the whole organism', 0.42857142857142855, 3.008048030199787, 1.1354133350961642, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(92213, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0101110', 'abnormal cell-free extract', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92214, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102860', 'abnormal mesenchymal stem cell morphology', 0.4666666666666667, 6.121988824155609, 1.6902449875504095, 'UPHENO:0084928', 'abnormal cell morphology'),
(92215, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0140803', 'abnormally necrotic pericyte', 0.4375, 6.121988824155609, 1.6365726719483247, 'UPHENO:0084928', 'abnormal cell morphology'),
(92216, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102768', 'abnormal ooplasm morphology', 0.41935483870967744, 4.8755453832354885, 1.4298893480995063, 'UPHENO:0086172', 'abnormal cell'),
(92217, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0103093', 'abnormal sperm entry point morphology', 0.43333333333333335, 4.8755453832354885, 1.453525484033692, 'UPHENO:0086172', 'abnormal cell'),
(92218, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102869', 'abnormal mucus secreting cell morphology', 0.5, 6.121988824155609, 1.7495697791393758, 'UPHENO:0084928', 'abnormal cell morphology'),
(92219, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102206', 'abnormal gastrula cell morphology', 0.4375, 6.121988824155609, 1.6365726719483247, 'UPHENO:0084928', 'abnormal cell morphology'),
(92220, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0101897', 'abnormal sensory epithelial cell morphology', 0.42424242424242425, 6.121988824155609, 1.6115853622891974, 'UPHENO:0084928', 'abnormal cell morphology'),
(92221, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0101921', 'abnormal chondroblast morphology', 0.5, 6.121988824155609, 1.7495697791393758, 'UPHENO:0084928', 'abnormal cell morphology'),
(92222, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102703', 'abnormal endoplasmic reticulum morphology', 0.4482758620689655, 4.8755453832354885, 1.478373873459029, 'UPHENO:0086172', 'abnormal cell'),
(92223, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0101713', 'abnormal anatomical entity in vitro morphology', 0.5217391304347826, 3.008048030199787, 1.2527634906807021, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(92224, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0107359', 'abnormal axial region morphology', 0.4444444444444444, 3.008048030199787, 1.1562483451423184, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(92225, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0107347', 'abnormal anterior-posterior axis morphology', 0.4444444444444444, 3.008048030199787, 1.1562483451423184, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(92226, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0100477', 'abnormal pericyte', 0.4166666666666667, 4.8755453832354885, 1.4252990012677296, 'UPHENO:0086172', 'abnormal cell'),
(92227, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0101435', 'abnormal paracrine cell', 0.4166666666666667, 4.8755453832354885, 1.4252990012677296, 'UPHENO:0086172', 'abnormal cell'),
(92228, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102081', 'abnormal lymphocyte morphology', 0.42424242424242425, 6.121988824155609, 1.6115853622891974, 'UPHENO:0084928', 'abnormal cell morphology'),
(92229, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0141314', 'abnormal Roux spot morphology', 0.41935483870967744, 4.8755453832354885, 1.4298893480995063, 'UPHENO:0086172', 'abnormal cell'),
(92230, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102998', 'abnormal morula cell morphology', 0.4375, 6.121988824155609, 1.6365726719483247, 'UPHENO:0084928', 'abnormal cell morphology'),
(92231, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0101969', 'abnormal zygote morphology', 0.5, 6.121988824155609, 1.7495697791393758, 'UPHENO:0084928', 'abnormal cell morphology'),
(92232, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0101638', 'abnormal anatomical structure morphology', 0.5217391304347826, 3.008048030199787, 1.2527634906807021, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(92233, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0140567', 'abnormally necrotic postero-ventral region', 0.42857142857142855, 3.008048030199787, 1.1354133350961642, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(92234, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0103095', 'abnormal right-ventral blastomere morphology', 0.4117647058823529, 6.121988824155609, 1.5877087036334738, 'UPHENO:0084928', 'abnormal cell morphology'),
(92235, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0140566', 'abnormally necrotic apical region', 0.41379310344827586, 3.008048030199787, 1.1156655097912829, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(92236, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0107426', 'abnormal yolk platelet morphology', 0.41935483870967744, 4.8755453832354885, 1.4298893480995063, 'UPHENO:0086172', 'abnormal cell'),
(92237, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102109', 'abnormal pericyte morphology', 0.5, 6.121988824155609, 1.7495697791393758, 'UPHENO:0084928', 'abnormal cell morphology'),
(92238, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102929', 'abnormal barrier cell morphology', 0.5, 6.121988824155609, 1.7495697791393758, 'UPHENO:0084928', 'abnormal cell morphology'),
(92239, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102178', 'abnormal whole organism morphology', 0.48, 3.008048030199787, 1.2016085279723583, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(92240, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0103010', 'abnormal blastomere D1 morphology', 0.4117647058823529, 6.121988824155609, 1.5877087036334738, 'UPHENO:0084928', 'abnormal cell morphology'),
(92241, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0100026', 'abnormal germ cell', 0.4166666666666667, 4.8755453832354885, 1.4252990012677296, 'UPHENO:0086172', 'abnormal cell'),
(92242, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0141154', 'abnormally necrotic barrier cell', 0.4375, 6.121988824155609, 1.6365726719483247, 'UPHENO:0084928', 'abnormal cell morphology'),
(92243, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102943', 'abnormal bottle cell morphology', 0.4117647058823529, 6.121988824155609, 1.5877087036334738, 'UPHENO:0084928', 'abnormal cell morphology'),
(92244, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102055', 'abnormal process morphology', 0.46153846153846156, 3.008048030199787, 1.178274102275107, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(92245, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0140239', 'abnormally necrotic absorptive cell', 0.4375, 6.121988824155609, 1.6365726719483247, 'UPHENO:0084928', 'abnormal cell morphology'),
(92246, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0103080', 'abnormal myelin accumulating cell morphology', 0.5, 6.121988824155609, 1.7495697791393758, 'UPHENO:0084928', 'abnormal cell morphology'),
(92247, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0101132', 'abnormal apoptotic cell', 0.4166666666666667, 4.8755453832354885, 1.4252990012677296, 'UPHENO:0086172', 'abnormal cell'),
(92248, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0103099', 'abnormal alkali secreting cell morphology', 0.5, 6.121988824155609, 1.7495697791393758, 'UPHENO:0084928', 'abnormal cell morphology'),
(92249, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0139981', 'abnormally necrotic early embryonic cell', 0.4117647058823529, 6.121988824155609, 1.5877087036334738, 'UPHENO:0084928', 'abnormal cell morphology'),
(92250, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0101976', 'abnormal portion of organism substance morphology', 0.5217391304347826, 3.008048030199787, 1.2527634906807021, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(92251, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0141147', 'abnormally necrotic alkali secreting cell', 0.4375, 6.121988824155609, 1.6365726719483247, 'UPHENO:0084928', 'abnormal cell morphology'),
(92252, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0103167', 'abnormal absorptive cell morphology', 0.5, 6.121988824155609, 1.7495697791393758, 'UPHENO:0084928', 'abnormal cell morphology'),
(92253, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0107357', 'abnormal proximal-distal axis morphology', 0.4444444444444444, 3.008048030199787, 1.1562483451423184, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(92254, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102189', 'abnormal prime meridian morphology', 0.41379310344827586, 3.008048030199787, 1.1156655097912829, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(92255, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0100172', 'abnormal stem cell', 0.4166666666666667, 4.8755453832354885, 1.4252990012677296, 'UPHENO:0086172', 'abnormal cell'),
(92256, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0103104', 'abnormal zygote cortex morphology', 0.43333333333333335, 4.8755453832354885, 1.453525484033692, 'UPHENO:0086172', 'abnormal cell'),
(92257, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0101333', 'abnormal barrier epithelial cell', 0.4166666666666667, 4.8755453832354885, 1.4252990012677296, 'UPHENO:0086172', 'abnormal cell'),
(92258, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0140075', 'abnormally necrotic stem cell', 0.4375, 6.121988824155609, 1.6365726719483247, 'UPHENO:0084928', 'abnormal cell morphology'),
(92259, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0103201', 'abnormal activin-induced ectoderm morphology', 0.48, 3.008048030199787, 1.2016085279723583, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(92260, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0103145', 'abnormal basal body morphology', 0.4482758620689655, 4.8755453832354885, 1.478373873459029, 'UPHENO:0086172', 'abnormal cell'),
(92261, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0100704', 'abnormal Merkel cell', 0.4166666666666667, 4.8755453832354885, 1.4252990012677296, 'UPHENO:0086172', 'abnormal cell'),
(92262, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102979', 'abnormal hindlimb region morphology', 0.4444444444444444, 3.008048030199787, 1.1562483451423184, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(92263, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102608', 'abnormal multiciliated cell morphology', 0.4666666666666667, 6.121988824155609, 1.6902449875504095, 'UPHENO:0084928', 'abnormal cell morphology'),
(92264, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0100638', 'abnormal polar body', 0.4166666666666667, 4.8755453832354885, 1.4252990012677296, 'UPHENO:0086172', 'abnormal cell'),
(92265, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102832', 'abnormal joint region morphology', 0.4444444444444444, 3.008048030199787, 1.1562483451423184, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(92266, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0100691', 'abnormal keratin accumulating cell', 0.4166666666666667, 4.8755453832354885, 1.4252990012677296, 'UPHENO:0086172', 'abnormal cell'),
(92267, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0103067', 'abnormal paracrine cell morphology', 0.5, 6.121988824155609, 1.7495697791393758, 'UPHENO:0084928', 'abnormal cell morphology'),
(92268, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102297', 'abnormal egg jelly morphology', 0.42857142857142855, 3.008048030199787, 1.1354133350961642, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(92269, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0100549', 'abnormal mitotic cell', 0.4166666666666667, 4.8755453832354885, 1.4252990012677296, 'UPHENO:0086172', 'abnormal cell'),
(92270, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0140600', 'abnormally necrotic apoptotic cell', 0.4375, 6.121988824155609, 1.6365726719483247, 'UPHENO:0084928', 'abnormal cell morphology'),
(92271, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0101635', 'abnormal organism subdivision morphology', 0.42857142857142855, 3.008048030199787, 1.1354133350961642, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(92272, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0103202', 'abnormal forelimb region morphology', 0.4444444444444444, 3.008048030199787, 1.1562483451423184, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(92273, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0140709', 'abnormally necrotic acid secreting cell', 0.4375, 6.121988824155609, 1.6365726719483247, 'UPHENO:0084928', 'abnormal cell morphology'),
(92274, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0139718', 'abnormally necrotic anatomical structure', 0.48, 3.008048030199787, 1.2016085279723583, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(92275, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102183', 'abnormal oocyte cortex morphology', 0.41935483870967744, 4.8755453832354885, 1.4298893480995063, 'UPHENO:0086172', 'abnormal cell'),
(92276, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0128037', 'decreased size of the anatomical space', 0.41379310344827586, 3.008048030199787, 1.1156655097912829, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(92277, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0140010', 'abnormally necrotic zygote', 0.4375, 6.121988824155609, 1.6365726719483247, 'UPHENO:0084928', 'abnormal cell morphology'),
(92278, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102621', 'abnormal right blastomere morphology', 0.4117647058823529, 6.121988824155609, 1.5877087036334738, 'UPHENO:0084928', 'abnormal cell morphology'),
(92279, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102323', 'abnormal keratin accumulating cell morphology', 0.5, 6.121988824155609, 1.7495697791393758, 'UPHENO:0084928', 'abnormal cell morphology'),
(92280, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102416', 'abnormal left blastomere morphology', 0.4117647058823529, 6.121988824155609, 1.5877087036334738, 'UPHENO:0084928', 'abnormal cell morphology'),
(92281, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0139929', 'abnormally necrotic barrier epithelial cell', 0.4375, 6.121988824155609, 1.6365726719483247, 'UPHENO:0084928', 'abnormal cell morphology'),
(92282, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0101535', 'abnormal absorptive cell', 0.4166666666666667, 4.8755453832354885, 1.4252990012677296, 'UPHENO:0086172', 'abnormal cell'),
(92283, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0100258', 'abnormal organ part', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92284, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102306', 'abnormal secondary oogonium morphology', 0.4666666666666667, 6.121988824155609, 1.6902449875504095, 'UPHENO:0084928', 'abnormal cell morphology'),
(92285, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102047', 'abnormal secretory epithelial cell morphology', 0.42424242424242425, 6.121988824155609, 1.6115853622891974, 'UPHENO:0084928', 'abnormal cell morphology'),
(92286, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0140389', 'abnormally necrotic cell condensation', 0.41379310344827586, 3.008048030199787, 1.1156655097912829, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(92287, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102534', 'abnormal spermatocyte morphology', 0.4666666666666667, 6.121988824155609, 1.6902449875504095, 'UPHENO:0084928', 'abnormal cell morphology'),
(92288, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0101834', 'abnormal embryo morphology', 0.42857142857142855, 3.008048030199787, 1.1354133350961642, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(92289, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0100546', 'abnormal whole organism', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92290, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0101740', 'abnormal cell part morphology', 0.48148148148148145, 4.8755453832354885, 1.5321503888817247, 'UPHENO:0086172', 'abnormal cell'),
(92291, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0141007', 'abnormally necrotic electrically active cell', 0.4375, 6.121988824155609, 1.6365726719483247, 'UPHENO:0084928', 'abnormal cell morphology'),
(92292, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0140919', 'abnormally necrotic cementoblast', 0.4375, 6.121988824155609, 1.6365726719483247, 'UPHENO:0084928', 'abnormal cell morphology'),
(92293, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0140927', 'abnormally necrotic basal region', 0.41379310344827586, 3.008048030199787, 1.1156655097912829, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(92294, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0101467', 'abnormal alkali secreting cell', 0.4166666666666667, 4.8755453832354885, 1.4252990012677296, 'UPHENO:0086172', 'abnormal cell'),
(92295, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102896', 'abnormal mitotic spindle morphology', 0.4482758620689655, 4.8755453832354885, 1.478373873459029, 'UPHENO:0086172', 'abnormal cell'),
(92296, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0100653', 'abnormal myoblast', 0.4166666666666667, 4.8755453832354885, 1.4252990012677296, 'UPHENO:0086172', 'abnormal cell'),
(92297, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0103082', 'abnormal myeloid cell morphology', 0.42424242424242425, 6.121988824155609, 1.6115853622891974, 'UPHENO:0084928', 'abnormal cell morphology'),
(92298, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0100081', 'abnormal anatomical entity in vitro', 0.42857142857142855, 1.7901636446558942, 0.8759069531444602, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92299, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102532', 'abnormal angioblast morphology', 0.42424242424242425, 6.121988824155609, 1.6115853622891974, 'UPHENO:0084928', 'abnormal cell morphology'),
(92300, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0103100', 'abnormal stage I oocyte morphology', 0.4375, 6.121988824155609, 1.6365726719483247, 'UPHENO:0084928', 'abnormal cell morphology'),
(92301, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102334', 'abnormal glial cell morphology', 0.42424242424242425, 6.121988824155609, 1.6115853622891974, 'UPHENO:0084928', 'abnormal cell morphology'),
(92302, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0141289', 'abnormal spindle microtubule morphology', 0.41935483870967744, 4.8755453832354885, 1.4298893480995063, 'UPHENO:0086172', 'abnormal cell'),
(92303, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0101808', 'abnormal stage VI oocyte morphology', 0.4375, 6.121988824155609, 1.6365726719483247, 'UPHENO:0084928', 'abnormal cell morphology'),
(92304, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102549', 'abnormal stage III oocyte morphology', 0.4375, 6.121988824155609, 1.6365726719483247, 'UPHENO:0084928', 'abnormal cell morphology'),
(92305, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102965', 'abnormal barrier epithelial cell morphology', 0.5, 6.121988824155609, 1.7495697791393758, 'UPHENO:0084928', 'abnormal cell morphology'),
(92306, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0107354', 'abnormal ventral side morphology', 0.41379310344827586, 3.008048030199787, 1.1156655097912829, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(92307, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0100285', 'abnormal progenitor cell', 0.4166666666666667, 4.8755453832354885, 1.4252990012677296, 'UPHENO:0086172', 'abnormal cell'),
(92308, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0101850', 'abnormal epithelial cell morphology', 0.45161290322580644, 6.121988824155609, 1.6627594974598268, 'UPHENO:0084928', 'abnormal cell morphology'),
(92309, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0103179', 'abnormal lampbrush chromosome morphology', 0.4482758620689655, 4.8755453832354885, 1.478373873459029, 'UPHENO:0086172', 'abnormal cell'),
(92310, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0129982', 'increased size of the anatomical line', 0.4444444444444444, 3.008048030199787, 1.1562483451423184, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(92311, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0103041', 'abnormal perivitelline space morphology', 0.41935483870967744, 4.8755453832354885, 1.4298893480995063, 'UPHENO:0086172', 'abnormal cell'),
(92312, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0101828', 'abnormal neuron morphology', 0.42424242424242425, 6.121988824155609, 1.6115853622891974, 'UPHENO:0084928', 'abnormal cell morphology'),
(92313, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0141254', 'abnormally necrotic dorso-lateral region', 0.42857142857142855, 3.008048030199787, 1.1354133350961642, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(92314, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0103129', 'abnormal ciliary axoneme morphology', 0.41935483870967744, 4.8755453832354885, 1.4298893480995063, 'UPHENO:0086172', 'abnormal cell'),
(92315, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0101909', 'abnormal blastocoel morphology', 0.42857142857142855, 3.008048030199787, 1.1354133350961642, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(92316, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0103037', 'abnormal ring structure morphology', 0.41935483870967744, 4.8755453832354885, 1.4298893480995063, 'UPHENO:0086172', 'abnormal cell'),
(92317, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0141296', 'abnormal adherens junction morphology', 0.4482758620689655, 4.8755453832354885, 1.478373873459029, 'UPHENO:0086172', 'abnormal cell'),
(92318, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0129582', 'increased size of the portion of organism substance', 0.4444444444444444, 3.008048030199787, 1.1562483451423184, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(92319, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102061', 'abnormal spermatid morphology', 0.4666666666666667, 6.121988824155609, 1.6902449875504095, 'UPHENO:0084928', 'abnormal cell morphology'),
(92320, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0140144', 'abnormally necrotic portion of organism substance', 0.48, 3.008048030199787, 1.2016085279723583, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(92321, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0115758', 'abnormally decreased mobility of melanoblast', 0.4074074074074074, 4.8755453832354885, 1.4093733729147593, 'UPHENO:0086172', 'abnormal cell'),
(92322, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102356', 'abnormal kinetochore morphology', 0.4482758620689655, 4.8755453832354885, 1.478373873459029, 'UPHENO:0086172', 'abnormal cell'),
(92323, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102494', 'abnormal blastomere V1 morphology', 0.4117647058823529, 6.121988824155609, 1.5877087036334738, 'UPHENO:0084928', 'abnormal cell morphology'),
(92324, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0101702', 'abnormal anatomical system morphology', 0.42857142857142855, 3.008048030199787, 1.1354133350961642, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(92325, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0100533', 'abnormal melanoblast', 0.4166666666666667, 4.8755453832354885, 1.4252990012677296, 'UPHENO:0086172', 'abnormal cell'),
(92326, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102531', 'abnormal secondary spermatogonium morphology', 0.4666666666666667, 6.121988824155609, 1.6902449875504095, 'UPHENO:0084928', 'abnormal cell morphology'),
(92327, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102353', 'abnormal centromere morphology', 0.4482758620689655, 4.8755453832354885, 1.478373873459029, 'UPHENO:0086172', 'abnormal cell'),
(92328, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0141505', 'abnormal tadpole morphology', 0.4444444444444444, 3.008048030199787, 1.1562483451423184, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(92329, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0141277', 'abnormal actin cytoskeleton morphology', 0.4482758620689655, 4.8755453832354885, 1.478373873459029, 'UPHENO:0086172', 'abnormal cell'),
(92330, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0101642', 'abnormal multicellular anatomical structure morphology', 0.46153846153846156, 3.008048030199787, 1.178274102275107, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(92331, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0101804', 'abnormal stem cell morphology', 0.5, 6.121988824155609, 1.7495697791393758, 'UPHENO:0084928', 'abnormal cell morphology'),
(92332, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0100762', 'abnormal intersomitic region', 0.42857142857142855, 1.7901636446558942, 0.8759069531444602, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92333, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0100969', 'abnormal disaggregated/reaggregated ectoderm treated with activin', 0.47368421052631576, 1.7901636446558942, 0.9208540887305324, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92334, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0101241', 'abnormal nucleate erythrocyte', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92335, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0107264', 'abnormal anterior side', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92336, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0100268', 'abnormal circulatory system', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92337, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0141263', 'abnormal visually guided collision avoidance behavior', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92338, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0101535', 'abnormal absorptive cell', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92339, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0100915', 'abnormal dermal system', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92340, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0101411', 'abnormal marginal zone (sensu neural)', 0.42857142857142855, 1.7901636446558942, 0.8759069531444602, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92341, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0100026', 'abnormal germ cell', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92342, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0142056', 'abnormal main body axis', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92343, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0100477', 'abnormal pericyte', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92344, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0101406', 'abnormal cleavage furrow', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92345, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0100186', 'abnormal uveal tract', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92346, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0100337', 'abnormal zygote', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92347, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0100162', 'abnormal presumptive rhombomere', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92348, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0100531', 'abnormal proliferative region', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92349, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0100004', 'abnormal cell', 0.42857142857142855, 1.7901636446558942, 0.8759069531444602, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92350, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0101078', 'abnormal mucous gland', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92351, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0101297', 'abnormal barrier cell', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92352, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0101040', 'abnormal axial mesoderm', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92353, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0100384', 'abnormal amputated tissue', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92354, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0101157', 'abnormal female organism', 0.45, 1.7901636446558942, 0.8975375424432965, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92355, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0100545', 'abnormal male organism', 0.45, 1.7901636446558942, 0.8975375424432965, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92356, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:00000000', 'Xenopus phenotype', 0.47058823529411764, 1.6758249395539064, 0.8880447629295182, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92357, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0107261', 'abnormal dorsal-ventral axis', 0.45, 1.7901636446558942, 0.8975375424432965, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92358, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0100010', 'abnormal multicellular anatomical structure', 0.45, 1.7901636446558942, 0.8975375424432965, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92359, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0100339', 'abnormal circumblastoporal collar', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92360, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0101333', 'abnormal barrier epithelial cell', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92361, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0100028', 'abnormal anatomical cluster', 0.42857142857142855, 1.7901636446558942, 0.8759069531444602, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92362, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0100003', 'abnormal organism subdivision', 0.42857142857142855, 1.7901636446558942, 0.8759069531444602, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92363, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0100014', 'abnormal tissue', 0.42857142857142855, 1.7901636446558942, 0.8759069531444602, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92364, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0115505', 'dead whole organism', 0.45, 1.7901636446558942, 0.8975375424432965, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92365, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0100135', 'abnormal surface structure', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92366, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0101373', 'abnormal oxygen accumulating cell', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92367, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0100557', 'abnormal prime meridian', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92368, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0115508', 'abnormally peramorphic growth of whole organism', 0.45, 1.7901636446558942, 0.8975375424432965, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92369, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0141276', 'decreased surface breathing', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92370, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0101141', 'abnormal Keller explant', 0.47368421052631576, 1.7901636446558942, 0.9208540887305324, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92371, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0101503', 'abnormal organ cortex', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92372, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0100791', 'abnormal multiciliated cell precursor', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92373, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0100913', 'abnormal Brachets cleft', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92374, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0100912', 'abnormal trabecula', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92375, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0100060', 'abnormal regenerating tissue', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92376, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0141784', 'abnormal cellular hormone metabolic process', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92377, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0100786', 'abnormal presumptive axial mesoderm', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92378, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0100289', 'abnormal chondroblast', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92379, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0100742', 'abnormal musculoskeletal system', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92380, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0141770', 'abnormal urate homeostasis', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92381, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0100372', 'abnormal hematological system', 0.45454545454545453, 5.816527256141925, 1.6260000078471883, 'UPHENO:0004459', 'abnormal hematopoietic system'),
(92382, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0101570', 'abnormal forelimb region', 0.42857142857142855, 1.7901636446558942, 0.8759069531444602, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92383, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0101110', 'abnormal cell-free extract', 0.47368421052631576, 1.7901636446558942, 0.9208540887305324, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92384, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0107278', 'abnormal medial region', 0.42857142857142855, 1.7901636446558942, 0.8759069531444602, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92385, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0100807', 'abnormal matrix-based tissue', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92386, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0100251', 'abnormal proteinaceous extracellular matrix', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92387, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0100852', 'abnormal interdigital region', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92388, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0100192', 'abnormal epithelium', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92389, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0100084', 'abnormal anatomical group', 0.45, 1.7901636446558942, 0.8975375424432965, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92390, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0100781', 'abnormal presumptive ectoderm', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92391, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0100823', 'abnormal blood', 0.4166666666666667, 5.816527256141925, 1.5567764847249168, 'UPHENO:0004459', 'abnormal hematopoietic system'),
(92392, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0100394', 'abnormal marginal zone', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92393, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0101132', 'abnormal apoptotic cell', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92394, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0100667', 'abnormal vegetal yolk mass', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92395, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0107276', 'abnormal dorsal region', 0.42857142857142855, 1.7901636446558942, 0.8759069531444602, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92396, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0100802', 'abnormal exocrine cell', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92397, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0100009', 'abnormal multi-tissue structure', 0.42857142857142855, 1.7901636446558942, 0.8759069531444602, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92398, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0100533', 'abnormal melanoblast', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92399, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0101448', 'abnormal myelin accumulating cell', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92400, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0107266', 'abnormal dorsal side', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92401, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0100081', 'abnormal anatomical entity in vitro', 0.5, 1.7901636446558942, 0.9460876398769551, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92402, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0100754', 'abnormal electrically active cell', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92403, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0141748', 'abnormal gas homeostasis', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92404, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0131725', 'abnormal phosphorylation of RNA polymerase II C-terminal domain', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92405, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0100070', 'abnormal anatomical system', 0.42857142857142855, 1.7901636446558942, 0.8759069531444602, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92406, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0141264', 'abnormal schooling behavior', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92407, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0101200', 'abnormal joint region', 0.42857142857142855, 1.7901636446558942, 0.8759069531444602, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92408, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0100546', 'abnormal whole organism', 0.47368421052631576, 1.7901636446558942, 0.9208540887305324, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92409, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0100423', 'abnormal process', 0.45, 1.7901636446558942, 0.8975375424432965, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92410, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0100344', 'abnormal portion of organism substance', 0.5, 1.7901636446558942, 0.9460876398769551, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92411, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0107263', 'abnormal anatomical side', 0.42857142857142855, 1.7901636446558942, 0.8759069531444602, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92412, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0141772', 'abnormal water homeostasis', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92413, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0131723', 'abnormal pathway-restricted SMAD protein phosphorylation', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92414, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0101109', 'abnormal egg cell-free extract', 0.45, 1.7901636446558942, 0.8975375424432965, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92415, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0100151', 'abnormal primordium', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92416, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0141267', 'abnormal resting posture', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92417, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0141499', 'abnormal tadpole', 0.45, 1.7901636446558942, 0.8975375424432965, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92418, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0116434', 'abnormal biological process', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92419, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0100202', 'abnormal embryo', 0.45, 1.7901636446558942, 0.8975375424432965, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92420, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0100172', 'abnormal stem cell', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92421, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0100295', 'abnormal extracellular matrix', 0.42857142857142855, 1.7901636446558942, 0.8759069531444602, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92422, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0100258', 'abnormal organ part', 0.47368421052631576, 1.7901636446558942, 0.9208540887305324, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92423, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0141745', 'abnormal creatinine homeostasis', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92424, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0107273', 'abnormal basal region', 0.42857142857142855, 1.7901636446558942, 0.8759069531444602, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92425, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0115512', 'abnormally semi-erect whole organism', 0.45, 1.7901636446558942, 0.8975375424432965, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92426, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0107269', 'abnormal right side', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92427, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0100108', 'abnormal cell part', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92428, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0100573', 'abnormal extraembryonic structure', 0.45, 1.7901636446558942, 0.8975375424432965, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92429, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0141315', 'abnormal anatomical region', 0.45, 1.7901636446558942, 0.8975375424432965, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92430, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0100239', 'abnormal acellular anatomical structure', 0.45, 1.7901636446558942, 0.8975375424432965, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92431, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0100023', 'abnormal mesenchyme', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92432, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0100610', 'abnormal appendage', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92433, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0100665', 'abnormal egg jelly', 0.42857142857142855, 1.7901636446558942, 0.8759069531444602, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92434, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0101519', 'abnormal hypobranchial placode', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92435, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0100481', 'abnormal anatomical line', 0.5, 1.7901636446558942, 0.9460876398769551, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92436, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0107262', 'abnormal left-right axis', 0.45, 1.7901636446558942, 0.8975375424432965, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92437, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0100715', 'abnormal ciliated cell', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92438, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0101237', 'abnormal mucus secreting cell', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92439, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0100231', 'abnormal compound organ', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92440, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0141715', 'abnormal septum', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92441, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0107272', 'abnormal axial region', 0.42857142857142855, 1.7901636446558942, 0.8759069531444602, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92442, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0141743', 'abnormal chemical homeostasis within a tissue', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92443, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0141271', 'increased surface breathing', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92444, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0100691', 'abnormal keratin accumulating cell', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92445, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0100285', 'abnormal progenitor cell', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92446, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0131691', 'abnormal molecular function', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92447, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0100704', 'abnormal Merkel cell', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92448, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0141272', 'absent surface breathing', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92449, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0100293', 'abnormal duct', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92450, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0101004', 'abnormal acid secreting cell', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92451, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0116494', 'absent biological process', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92452, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0100643', 'abnormal thoracic region', 0.42857142857142855, 1.7901636446558942, 0.8759069531444602, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92453, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0100549', 'abnormal mitotic cell', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92454, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0141265', 'abnormal escape behavior', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92455, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0107267', 'abnormal ventral side', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92456, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0101435', 'abnormal paracrine cell', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92457, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0141266', 'abnormal surface breathing', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92458, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0100856', 'abnormal simple organ', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92459, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0101347', 'abnormal hindlimb region', 0.42857142857142855, 1.7901636446558942, 0.8759069531444602, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92460, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0100728', 'abnormal cell condensation', 0.45, 1.7901636446558942, 0.8975375424432965, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92461, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0107260', 'abnormal anterior-posterior axis', 0.45, 1.7901636446558942, 0.8975375424432965, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92462, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0100638', 'abnormal polar body', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92463, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0101569', 'abnormal activin-induced ectoderm', 0.47368421052631576, 1.7901636446558942, 0.9208540887305324, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92464, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0100282', 'abnormal pelvic girdle primordium', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92465, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0100277', 'abnormal blastocoel', 0.42857142857142855, 1.7901636446558942, 0.8759069531444602, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92466, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0100991', 'abnormal iliac process primordium', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92467, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0141738', 'abnormal carbon dioxide homeostasis', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92468, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0100999', 'abnormal serous membrane', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92469, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0107259', 'abnormal animal-vegetal axis', 0.45, 1.7901636446558942, 0.8975375424432965, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92470, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0107271', 'abnormal apical region', 0.42857142857142855, 1.7901636446558942, 0.8759069531444602, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92471, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0107265', 'abnormal posterior side', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92472, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0100062', 'abnormal anatomical space', 0.45, 1.7901636446558942, 0.8975375424432965, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92473, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0100006', 'abnormal anatomical structure', 0.5, 1.7901636446558942, 0.9460876398769551, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92474, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0107268', 'abnormal left side', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92475, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0101326', 'abnormal cementoblast', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92476, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0107258', 'abnormal anatomical axis', 0.47368421052631576, 1.7901636446558942, 0.9208540887305324, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92477, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0115509', 'abnormally semi-viable whole organism', 0.45, 1.7901636446558942, 0.8975375424432965, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92478, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0100104', 'abnormal embryonic structure', 0.42857142857142855, 1.7901636446558942, 0.8759069531444602, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92479, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0100653', 'abnormal myoblast', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92480, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0101467', 'abnormal alkali secreting cell', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92481, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0141771', 'abnormal urea homeostasis', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92482, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0107270', 'abnormal proximal-distal axis', 0.45, 1.7901636446558942, 0.8975375424432965, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92483, 'HP:0034192', 'Pulmonary thromboembolism', 'XPO:0100363', 'abnormal cardiovascular system', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92484, 'HP:0033828', 'Middle mediastinal mass', 'XPO:0101713', 'abnormal anatomical entity in vitro morphology', 0.40625, 3.067140347159989, 1.1162552423320329, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(92485, 'HP:0033828', 'Middle mediastinal mass', 'XPO:0101976', 'abnormal portion of organism substance morphology', 0.40625, 3.067140347159989, 1.1162552423320329, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(92486, 'HP:0033828', 'Middle mediastinal mass', 'XPO:0101949', 'abnormal respiratory system morphology', 0.41025641025641024, 9.214829845132515, 1.944336136934069, 'UPHENO:0020748', 'abnormal respiratory system morphology'),
(92487, 'HP:0033828', 'Middle mediastinal mass', 'XPO:0102113', 'abnormal anatomical line morphology', 0.40625, 3.067140347159989, 1.1162552423320329, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(92488, 'HP:0033828', 'Middle mediastinal mass', 'XPO:0101638', 'abnormal anatomical structure morphology', 0.40625, 3.067140347159989, 1.1162552423320329, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(92489, 'HP:0003570', 'Molybdenum cofactor deficiency', 'XPO:00000000', 'Xenopus phenotype', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92490, 'HP:0003570', 'Molybdenum cofactor deficiency', 'XPO:0141738', 'abnormal carbon dioxide homeostasis', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92491, 'HP:0003570', 'Molybdenum cofactor deficiency', 'XPO:0141263', 'abnormal visually guided collision avoidance behavior', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92492, 'HP:0003570', 'Molybdenum cofactor deficiency', 'XPO:0131723', 'abnormal pathway-restricted SMAD protein phosphorylation', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92493, 'HP:0003570', 'Molybdenum cofactor deficiency', 'XPO:0141265', 'abnormal escape behavior', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92494, 'HP:0003570', 'Molybdenum cofactor deficiency', 'XPO:0141264', 'abnormal schooling behavior', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92495, 'HP:0003570', 'Molybdenum cofactor deficiency', 'XPO:0141272', 'absent surface breathing', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92496, 'HP:0003570', 'Molybdenum cofactor deficiency', 'XPO:0141748', 'abnormal gas homeostasis', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92497, 'HP:0003570', 'Molybdenum cofactor deficiency', 'XPO:0141743', 'abnormal chemical homeostasis within a tissue', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92498, 'HP:0003570', 'Molybdenum cofactor deficiency', 'XPO:0141784', 'abnormal cellular hormone metabolic process', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92499, 'HP:0003570', 'Molybdenum cofactor deficiency', 'XPO:0141771', 'abnormal urea homeostasis', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92500, 'HP:0003570', 'Molybdenum cofactor deficiency', 'XPO:0141745', 'abnormal creatinine homeostasis', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92501, 'HP:0003570', 'Molybdenum cofactor deficiency', 'XPO:0141267', 'abnormal resting posture', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92502, 'HP:0003570', 'Molybdenum cofactor deficiency', 'XPO:0131725', 'abnormal phosphorylation of RNA polymerase II C-terminal domain', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92503, 'HP:0003570', 'Molybdenum cofactor deficiency', 'XPO:0141772', 'abnormal water homeostasis', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92504, 'HP:0003570', 'Molybdenum cofactor deficiency', 'XPO:0141266', 'abnormal surface breathing', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92505, 'HP:0003570', 'Molybdenum cofactor deficiency', 'XPO:0141770', 'abnormal urate homeostasis', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92506, 'HP:0007799', 'Conjunctival whitish salt-like deposits', 'XPO:0102657', 'abnormal conjunctiva morphology', 0.4126984126984127, 12.906707549770184, 2.3079379798757103, 'UPHENO:0020997', 'abnormal conjunctiva morphology'),
(92507, 'HP:0033667', 'Diminished mental health', 'XPO:0141784', 'abnormal cellular hormone metabolic process', 0.5333333333333333, 1.6758249395539064, 0.9453958435996092, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92508, 'HP:0033667', 'Diminished mental health', 'XPO:0100239', 'abnormal acellular anatomical structure', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92509, 'HP:0033667', 'Diminished mental health', 'XPO:0131722', 'abnormal determination of left/right symmetry', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92510, 'HP:0033667', 'Diminished mental health', 'XPO:0141771', 'abnormal urea homeostasis', 0.5333333333333333, 1.6758249395539064, 0.9453958435996092, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92511, 'HP:0033667', 'Diminished mental health', 'XPO:0107270', 'abnormal proximal-distal axis', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92512, 'HP:0033667', 'Diminished mental health', 'XPO:0107261', 'abnormal dorsal-ventral axis', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92513, 'HP:0033667', 'Diminished mental health', 'XPO:0100665', 'abnormal egg jelly', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92514, 'HP:0033667', 'Diminished mental health', 'XPO:0141266', 'abnormal surface breathing', 0.5333333333333333, 1.6758249395539064, 0.9453958435996092, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92515, 'HP:0033667', 'Diminished mental health', 'XPO:0107260', 'abnormal anterior-posterior axis', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92516, 'HP:0033667', 'Diminished mental health', 'XPO:0101200', 'abnormal joint region', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92517, 'HP:0033667', 'Diminished mental health', 'XPO:0131469', 'abnormal heart process', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92518, 'HP:0033667', 'Diminished mental health', 'XPO:0107272', 'abnormal axial region', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92519, 'HP:0033667', 'Diminished mental health', 'XPO:0141975', 'abnormal cilium motility', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92520, 'HP:0033667', 'Diminished mental health', 'XPO:0101157', 'abnormal female organism', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92521, 'HP:0033667', 'Diminished mental health', 'XPO:0100062', 'abnormal anatomical space', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92522, 'HP:0033667', 'Diminished mental health', 'XPO:0101347', 'abnormal hindlimb region', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92523, 'HP:0033667', 'Diminished mental health', 'XPO:0100003', 'abnormal organism subdivision', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92524, 'HP:0033667', 'Diminished mental health', 'XPO:0131744', 'abnormal apical constriction', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92525, 'HP:0033667', 'Diminished mental health', 'XPO:0107263', 'abnormal anatomical side', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92526, 'HP:0033667', 'Diminished mental health', 'XPO:0115505', 'dead whole organism', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92527, 'HP:0033667', 'Diminished mental health', 'XPO:0141600', 'absent metamorphosis', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92528, 'HP:0033667', 'Diminished mental health', 'XPO:0128000', 'absent behavior', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92529, 'HP:0033667', 'Diminished mental health', 'XPO:0131703', 'abnormal cell division', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92530, 'HP:0033667', 'Diminished mental health', 'XPO:0100014', 'abnormal tissue', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92531, 'HP:0033667', 'Diminished mental health', 'XPO:0101110', 'abnormal cell-free extract', 0.47058823529411764, 1.6758249395539064, 0.8880447629295182, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92532, 'HP:0033667', 'Diminished mental health', 'XPO:0100481', 'abnormal anatomical line', 0.5, 1.6758249395539064, 0.9153755894587495, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92533, 'HP:0033667', 'Diminished mental health', 'XPO:0141276', 'decreased surface breathing', 0.5, 1.6758249395539064, 0.9153755894587495, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92534, 'HP:0033667', 'Diminished mental health', 'XPO:0100545', 'abnormal male organism', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92535, 'HP:0033667', 'Diminished mental health', 'XPO:0141264', 'abnormal schooling behavior', 0.5333333333333333, 1.6758249395539064, 0.9453958435996092, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92536, 'HP:0033667', 'Diminished mental health', 'XPO:0131729', 'abnormal regulation of growth rate', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92537, 'HP:0033667', 'Diminished mental health', 'XPO:0141267', 'abnormal resting posture', 0.5333333333333333, 1.6758249395539064, 0.9453958435996092, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92538, 'HP:0033667', 'Diminished mental health', 'XPO:0100969', 'abnormal disaggregated/reaggregated ectoderm treated with activin', 0.47058823529411764, 1.6758249395539064, 0.8880447629295182, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92539, 'HP:0033667', 'Diminished mental health', 'XPO:0116434', 'abnormal biological process', 0.5, 1.6758249395539064, 0.9153755894587495, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92540, 'HP:0033667', 'Diminished mental health', 'XPO:0141738', 'abnormal carbon dioxide homeostasis', 0.5333333333333333, 1.6758249395539064, 0.9453958435996092, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92541, 'HP:0033667', 'Diminished mental health', 'XPO:0131723', 'abnormal pathway-restricted SMAD protein phosphorylation', 0.5333333333333333, 1.6758249395539064, 0.9453958435996092, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92542, 'HP:0033667', 'Diminished mental health', 'XPO:0141960', 'absent cilium motility in brain', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92543, 'HP:0033667', 'Diminished mental health', 'XPO:00000000', 'Xenopus phenotype', 0.5714285714285714, 1.6758249395539064, 0.9785776674202517, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92544, 'HP:0033667', 'Diminished mental health', 'XPO:0100573', 'abnormal extraembryonic structure', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92545, 'HP:0033667', 'Diminished mental health', 'XPO:0100277', 'abnormal blastocoel', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92546, 'HP:0033667', 'Diminished mental health', 'XPO:0115508', 'abnormally peramorphic growth of whole organism', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92547, 'HP:0033667', 'Diminished mental health', 'XPO:0100070', 'abnormal anatomical system', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92548, 'HP:0033667', 'Diminished mental health', 'XPO:0100258', 'abnormal organ part', 0.47058823529411764, 1.6758249395539064, 0.8880447629295182, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92549, 'HP:0033667', 'Diminished mental health', 'XPO:0141263', 'abnormal visually guided collision avoidance behavior', 0.5333333333333333, 1.6758249395539064, 0.9453958435996092, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92550, 'HP:0033667', 'Diminished mental health', 'XPO:0100084', 'abnormal anatomical group', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92551, 'HP:0033667', 'Diminished mental health', 'XPO:0116494', 'absent biological process', 0.5, 1.6758249395539064, 0.9153755894587495, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92552, 'HP:0033667', 'Diminished mental health', 'XPO:0100004', 'abnormal cell', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92553, 'HP:0033667', 'Diminished mental health', 'XPO:0100295', 'abnormal extracellular matrix', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92554, 'HP:0033667', 'Diminished mental health', 'XPO:0141772', 'abnormal water homeostasis', 0.5333333333333333, 1.6758249395539064, 0.9453958435996092, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92555, 'HP:0033667', 'Diminished mental health', 'XPO:0141724', 'abnormal prevention of polyspermy', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92556, 'HP:0033667', 'Diminished mental health', 'XPO:0101411', 'abnormal marginal zone (sensu neural)', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92557, 'HP:0033667', 'Diminished mental health', 'XPO:0133401', 'absent determination of left/right symmetry in lateral plate mesoderm', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92558, 'HP:0033667', 'Diminished mental health', 'XPO:0107278', 'abnormal medial region', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92559, 'HP:0033667', 'Diminished mental health', 'XPO:0107258', 'abnormal anatomical axis', 0.47058823529411764, 1.6758249395539064, 0.8880447629295182, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92560, 'HP:0033667', 'Diminished mental health', 'XPO:0133403', 'abnormal developmental process', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92561, 'HP:0033667', 'Diminished mental health', 'XPO:0141745', 'abnormal creatinine homeostasis', 0.5333333333333333, 1.6758249395539064, 0.9453958435996092, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92562, 'HP:0033667', 'Diminished mental health', 'XPO:0107271', 'abnormal apical region', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92563, 'HP:0033667', 'Diminished mental health', 'XPO:0141499', 'abnormal tadpole', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92564, 'HP:0033667', 'Diminished mental health', 'XPO:0141809', 'abnormal catalytic activity', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92565, 'HP:0033667', 'Diminished mental health', 'XPO:0107273', 'abnormal basal region', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92566, 'HP:0033667', 'Diminished mental health', 'XPO:0100104', 'abnormal embryonic structure', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92567, 'HP:0033667', 'Diminished mental health', 'XPO:0100546', 'abnormal whole organism', 0.47058823529411764, 1.6758249395539064, 0.8880447629295182, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92568, 'HP:0033667', 'Diminished mental health', 'XPO:0141964', 'absent cilium motility in olfactory pit', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92569, 'HP:0033667', 'Diminished mental health', 'XPO:0100762', 'abnormal intersomitic region', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92570, 'HP:0033667', 'Diminished mental health', 'XPO:0141315', 'abnormal anatomical region', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92571, 'HP:0033667', 'Diminished mental health', 'XPO:0100728', 'abnormal cell condensation', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92572, 'HP:0033667', 'Diminished mental health', 'XPO:0116433', 'abnormal axis specification', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92573, 'HP:0033667', 'Diminished mental health', 'XPO:0115509', 'abnormally semi-viable whole organism', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92574, 'HP:0033667', 'Diminished mental health', 'XPO:0115512', 'abnormally semi-erect whole organism', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92575, 'HP:0033667', 'Diminished mental health', 'XPO:0141272', 'absent surface breathing', 0.5333333333333333, 1.6758249395539064, 0.9453958435996092, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92576, 'HP:0033667', 'Diminished mental health', 'XPO:0131725', 'abnormal phosphorylation of RNA polymerase II C-terminal domain', 0.5333333333333333, 1.6758249395539064, 0.9453958435996092, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92577, 'HP:0033667', 'Diminished mental health', 'XPO:0131730', 'abnormal regulation of protein folding', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92578, 'HP:0033667', 'Diminished mental health', 'XPO:0141959', 'absent cilium motility in floor plate', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92579, 'HP:0033667', 'Diminished mental health', 'XPO:0100423', 'abnormal process', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92580, 'HP:0033667', 'Diminished mental health', 'XPO:0100009', 'abnormal multi-tissue structure', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92581, 'HP:0033667', 'Diminished mental health', 'XPO:0141271', 'increased surface breathing', 0.5, 1.6758249395539064, 0.9153755894587495, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92582, 'HP:0033667', 'Diminished mental health', 'XPO:0100081', 'abnormal anatomical entity in vitro', 0.5, 1.6758249395539064, 0.9153755894587495, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92583, 'HP:0033667', 'Diminished mental health', 'XPO:0133388', 'absent insulin receptor signaling pathway', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92584, 'HP:0033667', 'Diminished mental health', 'XPO:0100202', 'abnormal embryo', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92585, 'HP:0033667', 'Diminished mental health', 'XPO:0107262', 'abnormal left-right axis', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92586, 'HP:0033667', 'Diminished mental health', 'XPO:0100028', 'abnormal anatomical cluster', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92587, 'HP:0033667', 'Diminished mental health', 'XPO:0101109', 'abnormal egg cell-free extract', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92588, 'HP:0033667', 'Diminished mental health', 'XPO:0141770', 'abnormal urate homeostasis', 0.5333333333333333, 1.6758249395539064, 0.9453958435996092, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92589, 'HP:0033667', 'Diminished mental health', 'XPO:0100010', 'abnormal multicellular anatomical structure', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92590, 'HP:0033667', 'Diminished mental health', 'XPO:0100643', 'abnormal thoracic region', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92591, 'HP:0033667', 'Diminished mental health', 'XPO:0141748', 'abnormal gas homeostasis', 0.5333333333333333, 1.6758249395539064, 0.9453958435996092, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92592, 'HP:0033667', 'Diminished mental health', 'XPO:0131719', 'abnormal activation of meiosis', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92593, 'HP:0033667', 'Diminished mental health', 'XPO:0141776', 'abnormal metabolic process', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92594, 'HP:0033667', 'Diminished mental health', 'XPO:0100344', 'abnormal portion of organism substance', 0.5, 1.6758249395539064, 0.9153755894587495, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92595, 'HP:0033667', 'Diminished mental health', 'XPO:0101141', 'abnormal Keller explant', 0.47058823529411764, 1.6758249395539064, 0.8880447629295182, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92596, 'HP:0033667', 'Diminished mental health', 'XPO:0141265', 'abnormal escape behavior', 0.5333333333333333, 1.6758249395539064, 0.9453958435996092, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92597, 'HP:0033667', 'Diminished mental health', 'XPO:0131740', 'abnormal detection of nodal flow', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92598, 'HP:0033667', 'Diminished mental health', 'XPO:0141962', 'absent cilium motility in pronephric kidney', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92599, 'HP:0033667', 'Diminished mental health', 'XPO:0116429', 'abnormal behavior', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92600, 'HP:0033667', 'Diminished mental health', 'XPO:0131691', 'abnormal molecular function', 0.5, 1.6758249395539064, 0.9153755894587495, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92601, 'HP:0033667', 'Diminished mental health', 'XPO:0107276', 'abnormal dorsal region', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92602, 'HP:0033667', 'Diminished mental health', 'XPO:0100006', 'abnormal anatomical structure', 0.5, 1.6758249395539064, 0.9153755894587495, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92603, 'HP:0033667', 'Diminished mental health', 'XPO:0133340', 'abnormal cell adhesion', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92604, 'HP:0033667', 'Diminished mental health', 'XPO:0107259', 'abnormal animal-vegetal axis', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92605, 'HP:0033667', 'Diminished mental health', 'XPO:0141743', 'abnormal chemical homeostasis within a tissue', 0.5333333333333333, 1.6758249395539064, 0.9453958435996092, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92606, 'HP:0033667', 'Diminished mental health', 'XPO:0101569', 'abnormal activin-induced ectoderm', 0.47058823529411764, 1.6758249395539064, 0.8880447629295182, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92607, 'HP:0033667', 'Diminished mental health', 'XPO:0141754', 'abnormal homeostatic process', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92608, 'HP:0033667', 'Diminished mental health', 'XPO:0101570', 'abnormal forelimb region', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92609, 'HP:0033667', 'Diminished mental health', 'XPO:0141958', 'absent cilium motility in left-right organizer', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92610, 'HP:0410169', 'Abnormal morphology of the shoulder musculature', 'XPO:0107258', 'abnormal anatomical axis', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92611, 'HP:0410169', 'Abnormal morphology of the shoulder musculature', 'XPO:0100258', 'abnormal organ part', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92612, 'HP:0410169', 'Abnormal morphology of the shoulder musculature', 'XPO:0101110', 'abnormal cell-free extract', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92613, 'HP:0410169', 'Abnormal morphology of the shoulder musculature', 'XPO:0101569', 'abnormal activin-induced ectoderm', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92614, 'HP:0410169', 'Abnormal morphology of the shoulder musculature', 'XPO:0100344', 'abnormal portion of organism substance', 0.42857142857142855, 1.7901636446558942, 0.8759069531444602, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92615, 'HP:0410169', 'Abnormal morphology of the shoulder musculature', 'XPO:0100969', 'abnormal disaggregated/reaggregated ectoderm treated with activin', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92616, 'HP:0410169', 'Abnormal morphology of the shoulder musculature', 'XPO:0101141', 'abnormal Keller explant', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92617, 'HP:0410169', 'Abnormal morphology of the shoulder musculature', 'XPO:0100481', 'abnormal anatomical line', 0.42857142857142855, 1.7901636446558942, 0.8759069531444602, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92618, 'HP:0410169', 'Abnormal morphology of the shoulder musculature', 'XPO:0100006', 'abnormal anatomical structure', 0.42857142857142855, 1.7901636446558942, 0.8759069531444602, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92619, 'HP:0410169', 'Abnormal morphology of the shoulder musculature', 'XPO:0100546', 'abnormal whole organism', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92620, 'HP:0410169', 'Abnormal morphology of the shoulder musculature', 'XPO:0100081', 'abnormal anatomical entity in vitro', 0.42857142857142855, 1.7901636446558942, 0.8759069531444602, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92621, 'HP:0000089', 'Renal hypoplasia', 'XPO:0129202', 'decreased size of the mesonephric sinus', 0.44, 7.667568053596582, 1.8367716089874908, 'UPHENO:0076779', 'abnormal kidney morphology'),
(92622, 'HP:0033658', 'Rounded atelectasis', 'XPO:0101949', 'abnormal respiratory system morphology', 0.43243243243243246, 9.214829845132515, 1.996194200067125, 'UPHENO:0020748', 'abnormal respiratory system morphology'),
(92623, 'HP:0033658', 'Rounded atelectasis', 'XPO:0101713', 'abnormal anatomical entity in vitro morphology', 0.43333333333333335, 3.067140347159989, 1.1528634569783167, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(92624, 'HP:0033658', 'Rounded atelectasis', 'XPO:0102113', 'abnormal anatomical line morphology', 0.43333333333333335, 3.067140347159989, 1.1528634569783167, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(92625, 'HP:0033658', 'Rounded atelectasis', 'XPO:0102773', 'abnormal Keller explant morphology', 0.40625, 3.067140347159989, 1.1162552423320329, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(92626, 'HP:0033658', 'Rounded atelectasis', 'XPO:0140269', 'abnormally necrotic anatomical line', 0.40625, 3.067140347159989, 1.1162552423320329, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(92627, 'HP:0033658', 'Rounded atelectasis', 'XPO:0103201', 'abnormal activin-induced ectoderm morphology', 0.40625, 3.067140347159989, 1.1162552423320329, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(92628, 'HP:0033658', 'Rounded atelectasis', 'XPO:0102601', 'abnormal disaggregated/reaggregated ectoderm treated with activin morphology', 0.40625, 3.067140347159989, 1.1162552423320329, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(92629, 'HP:0033658', 'Rounded atelectasis', 'XPO:0107345', 'abnormal anatomical axis morphology', 0.40625, 3.067140347159989, 1.1162552423320329, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(92630, 'HP:0033658', 'Rounded atelectasis', 'XPO:0102742', 'abnormal cell-free extract morphology', 0.40625, 3.067140347159989, 1.1162552423320329, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(92631, 'HP:0033658', 'Rounded atelectasis', 'XPO:0141316', 'abnormal anatomical region morphology', 0.40625, 3.067140347159989, 1.1162552423320329, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(92632, 'HP:0033658', 'Rounded atelectasis', 'XPO:0102178', 'abnormal whole organism morphology', 0.40625, 3.067140347159989, 1.1162552423320329, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(92633, 'HP:0033658', 'Rounded atelectasis', 'XPO:0101694', 'abnormal anatomical space morphology', 0.40625, 3.067140347159989, 1.1162552423320329, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(92634, 'HP:0033658', 'Rounded atelectasis', 'XPO:0101638', 'abnormal anatomical structure morphology', 0.43333333333333335, 3.067140347159989, 1.1528634569783167, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(92635, 'HP:0033658', 'Rounded atelectasis', 'XPO:0101976', 'abnormal portion of organism substance morphology', 0.43333333333333335, 3.067140347159989, 1.1528634569783167, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(92636, 'HP:0033658', 'Rounded atelectasis', 'XPO:0101890', 'abnormal organ part morphology', 0.40625, 3.067140347159989, 1.1162552423320329, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(92637, 'HP:0033658', 'Rounded atelectasis', 'XPO:0139718', 'abnormally necrotic anatomical structure', 0.40625, 3.067140347159989, 1.1162552423320329, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(92638, 'HP:0033658', 'Rounded atelectasis', 'XPO:0140144', 'abnormally necrotic portion of organism substance', 0.40625, 3.067140347159989, 1.1162552423320329, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(92639, 'HP:0100749', 'Chest pain', 'XPO:0131719', 'abnormal activation of meiosis', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92640, 'HP:0100749', 'Chest pain', 'XPO:0141959', 'absent cilium motility in floor plate', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92641, 'HP:0100749', 'Chest pain', 'XPO:0101109', 'abnormal egg cell-free extract', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92642, 'HP:0100749', 'Chest pain', 'XPO:0101347', 'abnormal hindlimb region', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92643, 'HP:0100749', 'Chest pain', 'XPO:0115509', 'abnormally semi-viable whole organism', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92644, 'HP:0100749', 'Chest pain', 'XPO:0141276', 'decreased surface breathing', 0.5, 1.6758249395539064, 0.9153755894587495, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92645, 'HP:0100749', 'Chest pain', 'XPO:0141748', 'abnormal gas homeostasis', 0.5333333333333333, 1.6758249395539064, 0.9453958435996092, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92646, 'HP:0100749', 'Chest pain', 'XPO:0141272', 'absent surface breathing', 0.5333333333333333, 1.6758249395539064, 0.9453958435996092, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92647, 'HP:0100749', 'Chest pain', 'XPO:0100344', 'abnormal portion of organism substance', 0.5, 1.6758249395539064, 0.9153755894587495, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92648, 'HP:0100749', 'Chest pain', 'XPO:0116434', 'abnormal biological process', 0.5, 1.6758249395539064, 0.9153755894587495, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92649, 'HP:0100749', 'Chest pain', 'XPO:0100643', 'abnormal thoracic region', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92650, 'HP:0100749', 'Chest pain', 'XPO:0100004', 'abnormal cell', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92651, 'HP:0100749', 'Chest pain', 'XPO:0133388', 'absent insulin receptor signaling pathway', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92652, 'HP:0100749', 'Chest pain', 'XPO:0100258', 'abnormal organ part', 0.47058823529411764, 1.6758249395539064, 0.8880447629295182, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92653, 'HP:0100749', 'Chest pain', 'XPO:0100202', 'abnormal embryo', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92654, 'HP:0100749', 'Chest pain', 'XPO:0100545', 'abnormal male organism', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92655, 'HP:0100749', 'Chest pain', 'XPO:0100062', 'abnormal anatomical space', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92656, 'HP:0100749', 'Chest pain', 'XPO:0100239', 'abnormal acellular anatomical structure', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92657, 'HP:0100749', 'Chest pain', 'XPO:0141784', 'abnormal cellular hormone metabolic process', 0.5333333333333333, 1.6758249395539064, 0.9453958435996092, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92658, 'HP:0100749', 'Chest pain', 'XPO:0133401', 'absent determination of left/right symmetry in lateral plate mesoderm', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92659, 'HP:0100749', 'Chest pain', 'XPO:0131730', 'abnormal regulation of protein folding', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92660, 'HP:0100749', 'Chest pain', 'XPO:0141600', 'absent metamorphosis', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92661, 'HP:0100749', 'Chest pain', 'XPO:0116494', 'absent biological process', 0.5, 1.6758249395539064, 0.9153755894587495, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92662, 'HP:0100749', 'Chest pain', 'XPO:0107258', 'abnormal anatomical axis', 0.47058823529411764, 1.6758249395539064, 0.8880447629295182, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92663, 'HP:0100749', 'Chest pain', 'XPO:0107276', 'abnormal dorsal region', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92664, 'HP:0100749', 'Chest pain', 'XPO:0100070', 'abnormal anatomical system', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92665, 'HP:0100749', 'Chest pain', 'XPO:0141499', 'abnormal tadpole', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92666, 'HP:0100749', 'Chest pain', 'XPO:0100969', 'abnormal disaggregated/reaggregated ectoderm treated with activin', 0.47058823529411764, 1.6758249395539064, 0.8880447629295182, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92667, 'HP:0100749', 'Chest pain', 'XPO:0101411', 'abnormal marginal zone (sensu neural)', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92668, 'HP:0100749', 'Chest pain', 'XPO:0100104', 'abnormal embryonic structure', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92669, 'HP:0100749', 'Chest pain', 'XPO:0100295', 'abnormal extracellular matrix', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92670, 'HP:0100749', 'Chest pain', 'XPO:0141745', 'abnormal creatinine homeostasis', 0.5333333333333333, 1.6758249395539064, 0.9453958435996092, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92671, 'HP:0100749', 'Chest pain', 'XPO:0101570', 'abnormal forelimb region', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92672, 'HP:0100749', 'Chest pain', 'XPO:0131691', 'abnormal molecular function', 0.5, 1.6758249395539064, 0.9153755894587495, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92673, 'HP:0100749', 'Chest pain', 'XPO:00000000', 'Xenopus phenotype', 0.5714285714285714, 1.6758249395539064, 0.9785776674202517, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92674, 'HP:0100749', 'Chest pain', 'XPO:0101200', 'abnormal joint region', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92675, 'HP:0100749', 'Chest pain', 'XPO:0141958', 'absent cilium motility in left-right organizer', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92676, 'HP:0100749', 'Chest pain', 'XPO:0100762', 'abnormal intersomitic region', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92677, 'HP:0100749', 'Chest pain', 'XPO:0131703', 'abnormal cell division', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92678, 'HP:0100749', 'Chest pain', 'XPO:0107272', 'abnormal axial region', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92679, 'HP:0100749', 'Chest pain', 'XPO:0107262', 'abnormal left-right axis', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92680, 'HP:0100749', 'Chest pain', 'XPO:0141962', 'absent cilium motility in pronephric kidney', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92681, 'HP:0100749', 'Chest pain', 'XPO:0141772', 'abnormal water homeostasis', 0.5333333333333333, 1.6758249395539064, 0.9453958435996092, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92682, 'HP:0100749', 'Chest pain', 'XPO:0100003', 'abnormal organism subdivision', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92683, 'HP:0100749', 'Chest pain', 'XPO:0100481', 'abnormal anatomical line', 0.5, 1.6758249395539064, 0.9153755894587495, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92684, 'HP:0100749', 'Chest pain', 'XPO:0141743', 'abnormal chemical homeostasis within a tissue', 0.5333333333333333, 1.6758249395539064, 0.9453958435996092, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92685, 'HP:0100749', 'Chest pain', 'XPO:0107263', 'abnormal anatomical side', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92686, 'HP:0100749', 'Chest pain', 'XPO:0115512', 'abnormally semi-erect whole organism', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92687, 'HP:0100749', 'Chest pain', 'XPO:0107261', 'abnormal dorsal-ventral axis', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92688, 'HP:0100749', 'Chest pain', 'XPO:0131725', 'abnormal phosphorylation of RNA polymerase II C-terminal domain', 0.5333333333333333, 1.6758249395539064, 0.9453958435996092, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92689, 'HP:0100749', 'Chest pain', 'XPO:0141264', 'abnormal schooling behavior', 0.5333333333333333, 1.6758249395539064, 0.9453958435996092, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92690, 'HP:0100749', 'Chest pain', 'XPO:0107259', 'abnormal animal-vegetal axis', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92691, 'HP:0100749', 'Chest pain', 'XPO:0141964', 'absent cilium motility in olfactory pit', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92692, 'HP:0100749', 'Chest pain', 'XPO:0100546', 'abnormal whole organism', 0.47058823529411764, 1.6758249395539064, 0.8880447629295182, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92693, 'HP:0100749', 'Chest pain', 'XPO:0115508', 'abnormally peramorphic growth of whole organism', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92694, 'HP:0100749', 'Chest pain', 'XPO:0100006', 'abnormal anatomical structure', 0.5, 1.6758249395539064, 0.9153755894587495, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92695, 'HP:0100749', 'Chest pain', 'XPO:0100014', 'abnormal tissue', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92696, 'HP:0100749', 'Chest pain', 'XPO:0131744', 'abnormal apical constriction', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92697, 'HP:0100749', 'Chest pain', 'XPO:0100081', 'abnormal anatomical entity in vitro', 0.5, 1.6758249395539064, 0.9153755894587495, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92698, 'HP:0100749', 'Chest pain', 'XPO:0100028', 'abnormal anatomical cluster', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92699, 'HP:0100749', 'Chest pain', 'XPO:0107278', 'abnormal medial region', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92700, 'HP:0100749', 'Chest pain', 'XPO:0116433', 'abnormal axis specification', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92701, 'HP:0100749', 'Chest pain', 'XPO:0133403', 'abnormal developmental process', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92702, 'HP:0100749', 'Chest pain', 'XPO:0141770', 'abnormal urate homeostasis', 0.5333333333333333, 1.6758249395539064, 0.9453958435996092, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92703, 'HP:0100749', 'Chest pain', 'XPO:0141315', 'abnormal anatomical region', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92704, 'HP:0100749', 'Chest pain', 'XPO:0107260', 'abnormal anterior-posterior axis', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92705, 'HP:0100749', 'Chest pain', 'XPO:0131469', 'abnormal heart process', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92706, 'HP:0100749', 'Chest pain', 'XPO:0100277', 'abnormal blastocoel', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92707, 'HP:0100749', 'Chest pain', 'XPO:0100084', 'abnormal anatomical group', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92708, 'HP:0100749', 'Chest pain', 'XPO:0116429', 'abnormal behavior', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92709, 'HP:0100749', 'Chest pain', 'XPO:0141738', 'abnormal carbon dioxide homeostasis', 0.5333333333333333, 1.6758249395539064, 0.9453958435996092, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92710, 'HP:0100749', 'Chest pain', 'XPO:0100665', 'abnormal egg jelly', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92711, 'HP:0100749', 'Chest pain', 'XPO:0141265', 'abnormal escape behavior', 0.5333333333333333, 1.6758249395539064, 0.9453958435996092, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92712, 'HP:0100749', 'Chest pain', 'XPO:0141271', 'increased surface breathing', 0.5, 1.6758249395539064, 0.9153755894587495, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92713, 'HP:0100749', 'Chest pain', 'XPO:0100728', 'abnormal cell condensation', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92714, 'HP:0100749', 'Chest pain', 'XPO:0107273', 'abnormal basal region', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92715, 'HP:0100749', 'Chest pain', 'XPO:0141263', 'abnormal visually guided collision avoidance behavior', 0.5333333333333333, 1.6758249395539064, 0.9453958435996092, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92716, 'HP:0100749', 'Chest pain', 'XPO:0141960', 'absent cilium motility in brain', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92717, 'HP:0100749', 'Chest pain', 'XPO:0101141', 'abnormal Keller explant', 0.47058823529411764, 1.6758249395539064, 0.8880447629295182, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92718, 'HP:0100749', 'Chest pain', 'XPO:0141771', 'abnormal urea homeostasis', 0.5333333333333333, 1.6758249395539064, 0.9453958435996092, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92719, 'HP:0100749', 'Chest pain', 'XPO:0141267', 'abnormal resting posture', 0.5333333333333333, 1.6758249395539064, 0.9453958435996092, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92720, 'HP:0100749', 'Chest pain', 'XPO:0141975', 'abnormal cilium motility', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92721, 'HP:0100749', 'Chest pain', 'XPO:0133340', 'abnormal cell adhesion', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92722, 'HP:0100749', 'Chest pain', 'XPO:0100423', 'abnormal process', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92723, 'HP:0100749', 'Chest pain', 'XPO:0141266', 'abnormal surface breathing', 0.5333333333333333, 1.6758249395539064, 0.9453958435996092, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92724, 'HP:0100749', 'Chest pain', 'XPO:0100009', 'abnormal multi-tissue structure', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92725, 'HP:0100749', 'Chest pain', 'XPO:0100573', 'abnormal extraembryonic structure', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92726, 'HP:0100749', 'Chest pain', 'XPO:0141809', 'abnormal catalytic activity', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92727, 'HP:0100749', 'Chest pain', 'XPO:0131722', 'abnormal determination of left/right symmetry', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92728, 'HP:0100749', 'Chest pain', 'XPO:0107271', 'abnormal apical region', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92729, 'HP:0100749', 'Chest pain', 'XPO:0101157', 'abnormal female organism', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92730, 'HP:0100749', 'Chest pain', 'XPO:0141754', 'abnormal homeostatic process', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92731, 'HP:0100749', 'Chest pain', 'XPO:0101110', 'abnormal cell-free extract', 0.47058823529411764, 1.6758249395539064, 0.8880447629295182, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92732, 'HP:0100749', 'Chest pain', 'XPO:0131723', 'abnormal pathway-restricted SMAD protein phosphorylation', 0.5333333333333333, 1.6758249395539064, 0.9453958435996092, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92733, 'HP:0100749', 'Chest pain', 'XPO:0100010', 'abnormal multicellular anatomical structure', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92734, 'HP:0100749', 'Chest pain', 'XPO:0141776', 'abnormal metabolic process', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92735, 'HP:0100749', 'Chest pain', 'XPO:0101569', 'abnormal activin-induced ectoderm', 0.47058823529411764, 1.6758249395539064, 0.8880447629295182, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92736, 'HP:0100749', 'Chest pain', 'XPO:0141724', 'abnormal prevention of polyspermy', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92737, 'HP:0100749', 'Chest pain', 'XPO:0115505', 'dead whole organism', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92738, 'HP:0100749', 'Chest pain', 'XPO:0107270', 'abnormal proximal-distal axis', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92739, 'HP:0100749', 'Chest pain', 'XPO:0131729', 'abnormal regulation of growth rate', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92740, 'HP:0100749', 'Chest pain', 'XPO:0128000', 'absent behavior', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92741, 'HP:0100749', 'Chest pain', 'XPO:0131740', 'abnormal detection of nodal flow', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92742, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0107260', 'abnormal anterior-posterior axis', 0.42857142857142855, 1.7901636446558942, 0.8759069531444602, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92743, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0100638', 'abnormal polar body', 0.45454545454545453, 4.8755453832354885, 1.4886762550601012, 'UPHENO:0086172', 'abnormal cell'),
(92744, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0101220', 'abnormal centriole', 0.4166666666666667, 4.8755453832354885, 1.4252990012677296, 'UPHENO:0086172', 'abnormal cell'),
(92745, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0100014', 'abnormal tissue', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92746, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0101513', 'abnormal basal body', 0.43478260869565216, 4.8755453832354885, 1.4559540997356917, 'UPHENO:0086172', 'abnormal cell'),
(92747, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0107312', 'abnormal filopodium', 0.43478260869565216, 4.8755453832354885, 1.4559540997356917, 'UPHENO:0086172', 'abnormal cell'),
(92748, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0100258', 'abnormal organ part', 0.45, 1.7901636446558942, 0.8975375424432965, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92749, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0141784', 'abnormal cellular hormone metabolic process', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92750, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0141272', 'absent surface breathing', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92751, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0100337', 'abnormal zygote', 0.45454545454545453, 4.8755453832354885, 1.4886762550601012, 'UPHENO:0086172', 'abnormal cell'),
(92752, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0100081', 'abnormal anatomical entity in vitro', 0.47368421052631576, 1.7901636446558942, 0.9208540887305324, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92753, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0101569', 'abnormal activin-induced ectoderm', 0.45, 1.7901636446558942, 0.8975375424432965, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92754, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0100009', 'abnormal multi-tissue structure', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92755, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0107270', 'abnormal proximal-distal axis', 0.42857142857142855, 1.7901636446558942, 0.8759069531444602, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92756, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0141738', 'abnormal carbon dioxide homeostasis', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92757, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0100239', 'abnormal acellular anatomical structure', 0.42857142857142855, 1.7901636446558942, 0.8759069531444602, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92758, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0100546', 'abnormal whole organism', 0.45, 1.7901636446558942, 0.8975375424432965, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92759, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0131675', 'abnormal spindle microtubule', 0.4166666666666667, 4.8755453832354885, 1.4252990012677296, 'UPHENO:0086172', 'abnormal cell'),
(92760, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0115508', 'abnormally peramorphic growth of whole organism', 0.42857142857142855, 1.7901636446558942, 0.8759069531444602, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92761, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0100533', 'abnormal melanoblast', 0.45454545454545453, 4.8755453832354885, 1.4886762550601012, 'UPHENO:0086172', 'abnormal cell'),
(92762, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0115505', 'dead whole organism', 0.42857142857142855, 1.7901636446558942, 0.8759069531444602, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92763, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0100704', 'abnormal Merkel cell', 0.45454545454545453, 4.8755453832354885, 1.4886762550601012, 'UPHENO:0086172', 'abnormal cell'),
(92764, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0100172', 'abnormal stem cell', 0.45454545454545453, 4.8755453832354885, 1.4886762550601012, 'UPHENO:0086172', 'abnormal cell'),
(92765, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0107261', 'abnormal dorsal-ventral axis', 0.42857142857142855, 1.7901636446558942, 0.8759069531444602, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92766, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0107263', 'abnormal anatomical side', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92767, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0101411', 'abnormal marginal zone (sensu neural)', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92768, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0101241', 'abnormal nucleate erythrocyte', 0.45454545454545453, 4.8755453832354885, 1.4886762550601012, 'UPHENO:0086172', 'abnormal cell'),
(92769, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0100899', 'abnormal secondary spermatogonium', 0.43478260869565216, 4.8755453832354885, 1.4559540997356917, 'UPHENO:0086172', 'abnormal cell'),
(92770, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0101061', 'abnormal plasma membrane', 0.43478260869565216, 4.8755453832354885, 1.4559540997356917, 'UPHENO:0086172', 'abnormal cell'),
(92771, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0100907', 'abnormal cytoplasm', 0.43478260869565216, 4.8755453832354885, 1.4559540997356917, 'UPHENO:0086172', 'abnormal cell'),
(92772, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0141770', 'abnormal urate homeostasis', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92773, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0107271', 'abnormal apical region', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92774, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0101141', 'abnormal Keller explant', 0.45, 1.7901636446558942, 0.8975375424432965, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92775, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0100888', 'abnormal microtubule', 0.43478260869565216, 4.8755453832354885, 1.4559540997356917, 'UPHENO:0086172', 'abnormal cell'),
(92776, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0100070', 'abnormal anatomical system', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92777, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0115509', 'abnormally semi-viable whole organism', 0.42857142857142855, 1.7901636446558942, 0.8759069531444602, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92778, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0107272', 'abnormal axial region', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92779, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0100003', 'abnormal organism subdivision', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92780, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0115512', 'abnormally semi-erect whole organism', 0.42857142857142855, 1.7901636446558942, 0.8759069531444602, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92781, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0107259', 'abnormal animal-vegetal axis', 0.42857142857142855, 1.7901636446558942, 0.8759069531444602, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92782, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0100956', 'abnormal centrosome', 0.43478260869565216, 4.8755453832354885, 1.4559540997356917, 'UPHENO:0086172', 'abnormal cell'),
(92783, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0131677', 'abnormal actin filament', 0.4166666666666667, 4.8755453832354885, 1.4252990012677296, 'UPHENO:0086172', 'abnormal cell'),
(92784, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0100573', 'abnormal extraembryonic structure', 0.42857142857142855, 1.7901636446558942, 0.8759069531444602, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92785, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0100004', 'abnormal cell', 0.47619047619047616, 4.8755453832354885, 1.5237087247014058, 'UPHENO:0086172', 'abnormal cell'),
(92786, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0101333', 'abnormal barrier epithelial cell', 0.45454545454545453, 4.8755453832354885, 1.4886762550601012, 'UPHENO:0086172', 'abnormal cell'),
(92787, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0100545', 'abnormal male organism', 0.42857142857142855, 1.7901636446558942, 0.8759069531444602, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92788, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0101535', 'abnormal absorptive cell', 0.45454545454545453, 4.8755453832354885, 1.4886762550601012, 'UPHENO:0086172', 'abnormal cell'),
(92789, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0100902', 'abnormal spermatocyte', 0.43478260869565216, 4.8755453832354885, 1.4559540997356917, 'UPHENO:0086172', 'abnormal cell'),
(92790, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0101004', 'abnormal acid secreting cell', 0.45454545454545453, 4.8755453832354885, 1.4886762550601012, 'UPHENO:0086172', 'abnormal cell'),
(92791, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0101467', 'abnormal alkali secreting cell', 0.45454545454545453, 4.8755453832354885, 1.4886762550601012, 'UPHENO:0086172', 'abnormal cell'),
(92792, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0100626', 'abnormal primordial germ cell', 0.43478260869565216, 4.8755453832354885, 1.4559540997356917, 'UPHENO:0086172', 'abnormal cell'),
(92793, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0100026', 'abnormal germ cell', 0.45454545454545453, 4.8755453832354885, 1.4886762550601012, 'UPHENO:0086172', 'abnormal cell'),
(92794, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0100392', 'abnormal cilium', 0.4166666666666667, 4.8755453832354885, 1.4252990012677296, 'UPHENO:0086172', 'abnormal cell'),
(92795, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0141264', 'abnormal schooling behavior', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92796, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0100308', 'abnormal early embryonic cell', 0.43478260869565216, 4.8755453832354885, 1.4559540997356917, 'UPHENO:0086172', 'abnormal cell'),
(92797, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0101326', 'abnormal cementoblast', 0.45454545454545453, 4.8755453832354885, 1.4886762550601012, 'UPHENO:0086172', 'abnormal cell'),
(92798, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0107276', 'abnormal dorsal region', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92799, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0100643', 'abnormal thoracic region', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92800, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0100202', 'abnormal embryo', 0.42857142857142855, 1.7901636446558942, 0.8759069531444602, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92801, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0101240', 'abnormal ciliated non-epidermal cell', 0.43478260869565216, 4.8755453832354885, 1.4559540997356917, 'UPHENO:0086172', 'abnormal cell'),
(92802, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0141263', 'abnormal visually guided collision avoidance behavior', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92803, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0100025', 'abnormal oocyte', 0.43478260869565216, 4.8755453832354885, 1.4559540997356917, 'UPHENO:0086172', 'abnormal cell'),
(92804, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0100691', 'abnormal keratin accumulating cell', 0.45454545454545453, 4.8755453832354885, 1.4886762550601012, 'UPHENO:0086172', 'abnormal cell'),
(92805, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0131685', 'abnormal cortical actin cytoskeleton', 0.4166666666666667, 4.8755453832354885, 1.4252990012677296, 'UPHENO:0086172', 'abnormal cell'),
(92806, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0101472', 'abnormal zygote cortex', 0.4166666666666667, 4.8755453832354885, 1.4252990012677296, 'UPHENO:0086172', 'abnormal cell'),
(92807, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0141315', 'abnormal anatomical region', 0.42857142857142855, 1.7901636446558942, 0.8759069531444602, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92808, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:00000000', 'Xenopus phenotype', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92809, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0101347', 'abnormal hindlimb region', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92810, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0100674', 'abnormal secondary oogonium', 0.43478260869565216, 4.8755453832354885, 1.4559540997356917, 'UPHENO:0086172', 'abnormal cell'),
(92811, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0101297', 'abnormal barrier cell', 0.45454545454545453, 4.8755453832354885, 1.4886762550601012, 'UPHENO:0086172', 'abnormal cell'),
(92812, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0100429', 'abnormal spermatid', 0.43478260869565216, 4.8755453832354885, 1.4559540997356917, 'UPHENO:0086172', 'abnormal cell'),
(92813, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0101113', 'abnormal stage IV oocyte', 0.4166666666666667, 4.8755453832354885, 1.4252990012677296, 'UPHENO:0086172', 'abnormal cell'),
(92814, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0107284', 'abnormal migrating myoblast', 0.43478260869565216, 4.8755453832354885, 1.4559540997356917, 'UPHENO:0086172', 'abnormal cell'),
(92815, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0100277', 'abnormal blastocoel', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92816, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0100549', 'abnormal mitotic cell', 0.45454545454545453, 4.8755453832354885, 1.4886762550601012, 'UPHENO:0086172', 'abnormal cell'),
(92817, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0101264', 'abnormal mitotic spindle', 0.43478260869565216, 4.8755453832354885, 1.4559540997356917, 'UPHENO:0086172', 'abnormal cell'),
(92818, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0100010', 'abnormal multicellular anatomical structure', 0.42857142857142855, 1.7901636446558942, 0.8759069531444602, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92819, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0107262', 'abnormal left-right axis', 0.42857142857142855, 1.7901636446558942, 0.8759069531444602, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92820, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0100894', 'abnormal nucleus', 0.43478260869565216, 4.8755453832354885, 1.4559540997356917, 'UPHENO:0086172', 'abnormal cell'),
(92821, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0142057', 'abnormal desmosome', 0.43478260869565216, 4.8755453832354885, 1.4559540997356917, 'UPHENO:0086172', 'abnormal cell'),
(92822, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0100515', 'abnormal somatic stem cell', 0.43478260869565216, 4.8755453832354885, 1.4559540997356917, 'UPHENO:0086172', 'abnormal cell'),
(92823, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0100084', 'abnormal anatomical group', 0.42857142857142855, 1.7901636446558942, 0.8759069531444602, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92824, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0100724', 'abnormal kinetochore', 0.43478260869565216, 4.8755453832354885, 1.4559540997356917, 'UPHENO:0086172', 'abnormal cell'),
(92825, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0107258', 'abnormal anatomical axis', 0.45, 1.7901636446558942, 0.8975375424432965, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92826, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0101200', 'abnormal joint region', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92827, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0100791', 'abnormal multiciliated cell precursor', 0.45454545454545453, 4.8755453832354885, 1.4886762550601012, 'UPHENO:0086172', 'abnormal cell'),
(92828, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0100481', 'abnormal anatomical line', 0.47368421052631576, 1.7901636446558942, 0.9208540887305324, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92829, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0101366', 'abnormal morula cell', 0.4166666666666667, 4.8755453832354885, 1.4252990012677296, 'UPHENO:0086172', 'abnormal cell'),
(92830, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0141748', 'abnormal gas homeostasis', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92831, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0141771', 'abnormal urea homeostasis', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92832, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0101468', 'abnormal stage I oocyte', 0.4166666666666667, 4.8755453832354885, 1.4252990012677296, 'UPHENO:0086172', 'abnormal cell'),
(92833, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0141772', 'abnormal water homeostasis', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92834, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0101132', 'abnormal apoptotic cell', 0.45454545454545453, 4.8755453832354885, 1.4886762550601012, 'UPHENO:0086172', 'abnormal cell'),
(92835, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0100917', 'abnormal stage III oocyte', 0.4166666666666667, 4.8755453832354885, 1.4252990012677296, 'UPHENO:0086172', 'abnormal cell'),
(92836, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0101109', 'abnormal egg cell-free extract', 0.42857142857142855, 1.7901636446558942, 0.8759069531444602, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92837, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0100028', 'abnormal anatomical cluster', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92838, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0131725', 'abnormal phosphorylation of RNA polymerase II C-terminal domain', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92839, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0101498', 'abnormal stage II oocyte', 0.4166666666666667, 4.8755453832354885, 1.4252990012677296, 'UPHENO:0086172', 'abnormal cell'),
(92840, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0141265', 'abnormal escape behavior', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92841, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0131723', 'abnormal pathway-restricted SMAD protein phosphorylation', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92842, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0141745', 'abnormal creatinine homeostasis', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92843, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0100104', 'abnormal embryonic structure', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92844, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0100307', 'abnormal blastomere', 0.4166666666666667, 4.8755453832354885, 1.4252990012677296, 'UPHENO:0086172', 'abnormal cell'),
(92845, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0100762', 'abnormal intersomitic region', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92846, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0100477', 'abnormal pericyte', 0.45454545454545453, 4.8755453832354885, 1.4886762550601012, 'UPHENO:0086172', 'abnormal cell'),
(92847, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0141499', 'abnormal tadpole', 0.42857142857142855, 1.7901636446558942, 0.8759069531444602, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92848, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0100754', 'abnormal electrically active cell', 0.45454545454545453, 4.8755453832354885, 1.4886762550601012, 'UPHENO:0086172', 'abnormal cell'),
(92849, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0141267', 'abnormal resting posture', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92850, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0100976', 'abnormal multiciliated cell', 0.43478260869565216, 4.8755453832354885, 1.4559540997356917, 'UPHENO:0086172', 'abnormal cell'),
(92851, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0100344', 'abnormal portion of organism substance', 0.47368421052631576, 1.7901636446558942, 0.9208540887305324, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92852, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0100423', 'abnormal process', 0.42857142857142855, 1.7901636446558942, 0.8759069531444602, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92853, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0131667', 'abnormal actin cytoskeleton', 0.43478260869565216, 4.8755453832354885, 1.4559540997356917, 'UPHENO:0086172', 'abnormal cell'),
(92854, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0100289', 'abnormal chondroblast', 0.45454545454545453, 4.8755453832354885, 1.4886762550601012, 'UPHENO:0086172', 'abnormal cell'),
(92855, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0107273', 'abnormal basal region', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92856, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0141743', 'abnormal chemical homeostasis within a tissue', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92857, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0141266', 'abnormal surface breathing', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92858, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0100062', 'abnormal anatomical space', 0.42857142857142855, 1.7901636446558942, 0.8759069531444602, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92859, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0101409', 'abnormal perivitelline space', 0.4166666666666667, 4.8755453832354885, 1.4252990012677296, 'UPHENO:0086172', 'abnormal cell'),
(92860, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0100437', 'abnormal proepicardium', 0.43478260869565216, 4.8755453832354885, 1.4559540997356917, 'UPHENO:0086172', 'abnormal cell'),
(92861, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0100108', 'abnormal cell part', 0.45454545454545453, 4.8755453832354885, 1.4886762550601012, 'UPHENO:0086172', 'abnormal cell'),
(92862, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0101480', 'abnormal stage V oocyte', 0.4166666666666667, 4.8755453832354885, 1.4252990012677296, 'UPHENO:0086172', 'abnormal cell'),
(92863, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0107278', 'abnormal medial region', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92864, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0100715', 'abnormal ciliated cell', 0.45454545454545453, 4.8755453832354885, 1.4886762550601012, 'UPHENO:0086172', 'abnormal cell'),
(92865, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0100006', 'abnormal anatomical structure', 0.47368421052631576, 1.7901636446558942, 0.9208540887305324, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92866, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0101228', 'abnormal mesenchymal stem cell', 0.43478260869565216, 4.8755453832354885, 1.4559540997356917, 'UPHENO:0086172', 'abnormal cell'),
(92867, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0101461', 'abnormal sperm entry point', 0.4166666666666667, 4.8755453832354885, 1.4252990012677296, 'UPHENO:0086172', 'abnormal cell'),
(92868, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0101373', 'abnormal oxygen accumulating cell', 0.45454545454545453, 4.8755453832354885, 1.4886762550601012, 'UPHENO:0086172', 'abnormal cell'),
(92869, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0100653', 'abnormal myoblast', 0.45454545454545453, 4.8755453832354885, 1.4886762550601012, 'UPHENO:0086172', 'abnormal cell'),
(92870, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0101570', 'abnormal forelimb region', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92871, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0100574', 'abnormal gastrula cell', 0.4166666666666667, 4.8755453832354885, 1.4252990012677296, 'UPHENO:0086172', 'abnormal cell'),
(92872, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0101071', 'abnormal endoplasmic reticulum', 0.43478260869565216, 4.8755453832354885, 1.4559540997356917, 'UPHENO:0086172', 'abnormal cell'),
(92873, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0101448', 'abnormal myelin accumulating cell', 0.45454545454545453, 4.8755453832354885, 1.4886762550601012, 'UPHENO:0086172', 'abnormal cell'),
(92874, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0100802', 'abnormal exocrine cell', 0.45454545454545453, 4.8755453832354885, 1.4886762550601012, 'UPHENO:0086172', 'abnormal cell'),
(92875, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0100665', 'abnormal egg jelly', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92876, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0101157', 'abnormal female organism', 0.42857142857142855, 1.7901636446558942, 0.8759069531444602, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92877, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0101237', 'abnormal mucus secreting cell', 0.45454545454545453, 4.8755453832354885, 1.4886762550601012, 'UPHENO:0086172', 'abnormal cell'),
(92878, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0100969', 'abnormal disaggregated/reaggregated ectoderm treated with activin', 0.45, 1.7901636446558942, 0.8975375424432965, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92879, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0100721', 'abnormal centromere', 0.43478260869565216, 4.8755453832354885, 1.4559540997356917, 'UPHENO:0086172', 'abnormal cell'),
(92880, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0100728', 'abnormal cell condensation', 0.42857142857142855, 1.7901636446558942, 0.8759069531444602, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92881, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0101110', 'abnormal cell-free extract', 0.45, 1.7901636446558942, 0.8975375424432965, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92882, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0101435', 'abnormal paracrine cell', 0.45454545454545453, 4.8755453832354885, 1.4886762550601012, 'UPHENO:0086172', 'abnormal cell'),
(92883, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0100176', 'abnormal stage VI oocyte', 0.4166666666666667, 4.8755453832354885, 1.4252990012677296, 'UPHENO:0086172', 'abnormal cell'),
(92884, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0131666', 'abnormal adherens junction', 0.43478260869565216, 4.8755453832354885, 1.4559540997356917, 'UPHENO:0086172', 'abnormal cell'),
(92885, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0100285', 'abnormal progenitor cell', 0.45454545454545453, 4.8755453832354885, 1.4886762550601012, 'UPHENO:0086172', 'abnormal cell'),
(92886, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0101547', 'abnormal lampbrush chromosome', 0.43478260869565216, 4.8755453832354885, 1.4559540997356917, 'UPHENO:0086172', 'abnormal cell'),
(92887, 'HP:0010998', 'Increased susceptibility to spontaneous sister chromatid exchange', 'XPO:0100295', 'abnormal extracellular matrix', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92888, 'HP:0034244', 'Gastric pseudomass', 'XPO:0101569', 'abnormal activin-induced ectoderm', 0.45, 1.7901636446558942, 0.8975375424432965, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92889, 'HP:0034244', 'Gastric pseudomass', 'XPO:0141265', 'abnormal escape behavior', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92890, 'HP:0034244', 'Gastric pseudomass', 'XPO:0107273', 'abnormal basal region', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92891, 'HP:0034244', 'Gastric pseudomass', 'XPO:0141745', 'abnormal creatinine homeostasis', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92892, 'HP:0034244', 'Gastric pseudomass', 'XPO:0101347', 'abnormal hindlimb region', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92893, 'HP:0034244', 'Gastric pseudomass', 'XPO:0100084', 'abnormal anatomical group', 0.42857142857142855, 1.7901636446558942, 0.8759069531444602, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92894, 'HP:0034244', 'Gastric pseudomass', 'XPO:0141771', 'abnormal urea homeostasis', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92895, 'HP:0034244', 'Gastric pseudomass', 'XPO:0100643', 'abnormal thoracic region', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92896, 'HP:0034244', 'Gastric pseudomass', 'XPO:0101109', 'abnormal egg cell-free extract', 0.42857142857142855, 1.7901636446558942, 0.8759069531444602, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92897, 'HP:0034244', 'Gastric pseudomass', 'XPO:0100070', 'abnormal anatomical system', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92898, 'HP:0034244', 'Gastric pseudomass', 'XPO:0100028', 'abnormal anatomical cluster', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92899, 'HP:0034244', 'Gastric pseudomass', 'XPO:0107259', 'abnormal animal-vegetal axis', 0.42857142857142855, 1.7901636446558942, 0.8759069531444602, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92900, 'HP:0034244', 'Gastric pseudomass', 'XPO:0100344', 'abnormal portion of organism substance', 0.47368421052631576, 1.7901636446558942, 0.9208540887305324, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92901, 'HP:0034244', 'Gastric pseudomass', 'XPO:0100423', 'abnormal process', 0.42857142857142855, 1.7901636446558942, 0.8759069531444602, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92902, 'HP:0034244', 'Gastric pseudomass', 'XPO:0100004', 'abnormal cell', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92903, 'HP:0034244', 'Gastric pseudomass', 'XPO:0131723', 'abnormal pathway-restricted SMAD protein phosphorylation', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92904, 'HP:0034244', 'Gastric pseudomass', 'XPO:0100277', 'abnormal blastocoel', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92905, 'HP:0034244', 'Gastric pseudomass', 'XPO:0100009', 'abnormal multi-tissue structure', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92906, 'HP:0034244', 'Gastric pseudomass', 'XPO:0101157', 'abnormal female organism', 0.42857142857142855, 1.7901636446558942, 0.8759069531444602, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92907, 'HP:0034244', 'Gastric pseudomass', 'XPO:0100295', 'abnormal extracellular matrix', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92908, 'HP:0034244', 'Gastric pseudomass', 'XPO:0100728', 'abnormal cell condensation', 0.42857142857142855, 1.7901636446558942, 0.8759069531444602, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92909, 'HP:0034244', 'Gastric pseudomass', 'XPO:0141770', 'abnormal urate homeostasis', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92910, 'HP:0034244', 'Gastric pseudomass', 'XPO:0141784', 'abnormal cellular hormone metabolic process', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92911, 'HP:0034244', 'Gastric pseudomass', 'XPO:0141772', 'abnormal water homeostasis', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92912, 'HP:0034244', 'Gastric pseudomass', 'XPO:0141267', 'abnormal resting posture', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92913, 'HP:0034244', 'Gastric pseudomass', 'XPO:0100258', 'abnormal organ part', 0.45, 1.7901636446558942, 0.8975375424432965, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92914, 'HP:0034244', 'Gastric pseudomass', 'XPO:0100546', 'abnormal whole organism', 0.45, 1.7901636446558942, 0.8975375424432965, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92915, 'HP:0034244', 'Gastric pseudomass', 'XPO:0141264', 'abnormal schooling behavior', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92916, 'HP:0034244', 'Gastric pseudomass', 'XPO:0131725', 'abnormal phosphorylation of RNA polymerase II C-terminal domain', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92917, 'HP:0034244', 'Gastric pseudomass', 'XPO:0115508', 'abnormally peramorphic growth of whole organism', 0.42857142857142855, 1.7901636446558942, 0.8759069531444602, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92918, 'HP:0034244', 'Gastric pseudomass', 'XPO:0101570', 'abnormal forelimb region', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92919, 'HP:0034244', 'Gastric pseudomass', 'XPO:0100573', 'abnormal extraembryonic structure', 0.42857142857142855, 1.7901636446558942, 0.8759069531444602, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92920, 'HP:0034244', 'Gastric pseudomass', 'XPO:0100014', 'abnormal tissue', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92921, 'HP:0034244', 'Gastric pseudomass', 'XPO:0107262', 'abnormal left-right axis', 0.42857142857142855, 1.7901636446558942, 0.8759069531444602, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92922, 'HP:0034244', 'Gastric pseudomass', 'XPO:0141499', 'abnormal tadpole', 0.42857142857142855, 1.7901636446558942, 0.8759069531444602, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92923, 'HP:0034244', 'Gastric pseudomass', 'XPO:0100545', 'abnormal male organism', 0.42857142857142855, 1.7901636446558942, 0.8759069531444602, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92924, 'HP:0034244', 'Gastric pseudomass', 'XPO:0141743', 'abnormal chemical homeostasis within a tissue', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92925, 'HP:0034244', 'Gastric pseudomass', 'XPO:0141266', 'abnormal surface breathing', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92926, 'HP:0034244', 'Gastric pseudomass', 'XPO:0100239', 'abnormal acellular anatomical structure', 0.42857142857142855, 1.7901636446558942, 0.8759069531444602, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92927, 'HP:0034244', 'Gastric pseudomass', 'XPO:0107278', 'abnormal medial region', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92928, 'HP:0034244', 'Gastric pseudomass', 'XPO:0107258', 'abnormal anatomical axis', 0.45, 1.7901636446558942, 0.8975375424432965, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92929, 'HP:0034244', 'Gastric pseudomass', 'XPO:0100003', 'abnormal organism subdivision', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92930, 'HP:0034244', 'Gastric pseudomass', 'XPO:0141315', 'abnormal anatomical region', 0.42857142857142855, 1.7901636446558942, 0.8759069531444602, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92931, 'HP:0034244', 'Gastric pseudomass', 'XPO:0107260', 'abnormal anterior-posterior axis', 0.42857142857142855, 1.7901636446558942, 0.8759069531444602, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92932, 'HP:0034244', 'Gastric pseudomass', 'XPO:0107263', 'abnormal anatomical side', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92933, 'HP:0034244', 'Gastric pseudomass', 'XPO:0100202', 'abnormal embryo', 0.42857142857142855, 1.7901636446558942, 0.8759069531444602, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92934, 'HP:0034244', 'Gastric pseudomass', 'XPO:0100104', 'abnormal embryonic structure', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92935, 'HP:0034244', 'Gastric pseudomass', 'XPO:0101411', 'abnormal marginal zone (sensu neural)', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92936, 'HP:0034244', 'Gastric pseudomass', 'XPO:0107270', 'abnormal proximal-distal axis', 0.42857142857142855, 1.7901636446558942, 0.8759069531444602, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92937, 'HP:0034244', 'Gastric pseudomass', 'XPO:0101110', 'abnormal cell-free extract', 0.45, 1.7901636446558942, 0.8975375424432965, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92938, 'HP:0034244', 'Gastric pseudomass', 'XPO:0100969', 'abnormal disaggregated/reaggregated ectoderm treated with activin', 0.45, 1.7901636446558942, 0.8975375424432965, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92939, 'HP:0034244', 'Gastric pseudomass', 'XPO:0100081', 'abnormal anatomical entity in vitro', 0.47368421052631576, 1.7901636446558942, 0.9208540887305324, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92940, 'HP:0034244', 'Gastric pseudomass', 'XPO:0100006', 'abnormal anatomical structure', 0.47368421052631576, 1.7901636446558942, 0.9208540887305324, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92941, 'HP:0034244', 'Gastric pseudomass', 'XPO:0115512', 'abnormally semi-erect whole organism', 0.42857142857142855, 1.7901636446558942, 0.8759069531444602, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92942, 'HP:0034244', 'Gastric pseudomass', 'XPO:0107261', 'abnormal dorsal-ventral axis', 0.42857142857142855, 1.7901636446558942, 0.8759069531444602, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92943, 'HP:0034244', 'Gastric pseudomass', 'XPO:0115505', 'dead whole organism', 0.42857142857142855, 1.7901636446558942, 0.8759069531444602, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92944, 'HP:0034244', 'Gastric pseudomass', 'XPO:0141272', 'absent surface breathing', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92945, 'HP:0034244', 'Gastric pseudomass', 'XPO:0107272', 'abnormal axial region', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92946, 'HP:0034244', 'Gastric pseudomass', 'XPO:0101200', 'abnormal joint region', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92947, 'HP:0034244', 'Gastric pseudomass', 'XPO:0101141', 'abnormal Keller explant', 0.45, 1.7901636446558942, 0.8975375424432965, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92948, 'HP:0034244', 'Gastric pseudomass', 'XPO:0107271', 'abnormal apical region', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92949, 'HP:0034244', 'Gastric pseudomass', 'XPO:0100481', 'abnormal anatomical line', 0.47368421052631576, 1.7901636446558942, 0.9208540887305324, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92950, 'HP:0034244', 'Gastric pseudomass', 'XPO:0115509', 'abnormally semi-viable whole organism', 0.42857142857142855, 1.7901636446558942, 0.8759069531444602, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92951, 'HP:0034244', 'Gastric pseudomass', 'XPO:0100665', 'abnormal egg jelly', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92952, 'HP:0034244', 'Gastric pseudomass', 'XPO:00000000', 'Xenopus phenotype', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92953, 'HP:0034244', 'Gastric pseudomass', 'XPO:0141748', 'abnormal gas homeostasis', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92954, 'HP:0034244', 'Gastric pseudomass', 'XPO:0141263', 'abnormal visually guided collision avoidance behavior', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92955, 'HP:0034244', 'Gastric pseudomass', 'XPO:0100762', 'abnormal intersomitic region', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92956, 'HP:0034244', 'Gastric pseudomass', 'XPO:0107276', 'abnormal dorsal region', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92957, 'HP:0034244', 'Gastric pseudomass', 'XPO:0141738', 'abnormal carbon dioxide homeostasis', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92958, 'HP:0034244', 'Gastric pseudomass', 'XPO:0100062', 'abnormal anatomical space', 0.42857142857142855, 1.7901636446558942, 0.8759069531444602, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92959, 'HP:0034244', 'Gastric pseudomass', 'XPO:0100010', 'abnormal multicellular anatomical structure', 0.42857142857142855, 1.7901636446558942, 0.8759069531444602, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92960, 'HP:0002832', 'Calcific stippling', 'XPO:0107269', 'abnormal right side', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92961, 'HP:0002832', 'Calcific stippling', 'XPO:0100289', 'abnormal chondroblast', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92962, 'HP:0002832', 'Calcific stippling', 'XPO:0101535', 'abnormal absorptive cell', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92963, 'HP:0002832', 'Calcific stippling', 'XPO:0101078', 'abnormal mucous gland', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92964, 'HP:0002832', 'Calcific stippling', 'XPO:0100172', 'abnormal stem cell', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92965, 'HP:0002832', 'Calcific stippling', 'XPO:0100999', 'abnormal serous membrane', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92966, 'HP:0002832', 'Calcific stippling', 'XPO:0141745', 'abnormal creatinine homeostasis', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92967, 'HP:0002832', 'Calcific stippling', 'XPO:0101109', 'abnormal egg cell-free extract', 0.45, 1.7901636446558942, 0.8975375424432965, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92968, 'HP:0002832', 'Calcific stippling', 'XPO:0141718', 'abnormal posterior notochord', 0.4166666666666667, 4.401455821078525, 1.3542303812311203, 'UPHENO:0002964', 'abnormal skeletal system'),
(92969, 'HP:0002832', 'Calcific stippling', 'XPO:0101237', 'abnormal mucus secreting cell', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92970, 'HP:0002832', 'Calcific stippling', 'XPO:0101297', 'abnormal barrier cell', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92971, 'HP:0002832', 'Calcific stippling', 'XPO:0100742', 'abnormal musculoskeletal system', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92972, 'HP:0002832', 'Calcific stippling', 'XPO:0101110', 'abnormal cell-free extract', 0.47368421052631576, 1.7901636446558942, 0.9208540887305324, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92973, 'HP:0002832', 'Calcific stippling', 'XPO:0100186', 'abnormal uveal tract', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92974, 'HP:0002832', 'Calcific stippling', 'XPO:0100202', 'abnormal embryo', 0.45, 1.7901636446558942, 0.8975375424432965, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92975, 'HP:0002832', 'Calcific stippling', 'XPO:0115509', 'abnormally semi-viable whole organism', 0.45, 1.7901636446558942, 0.8975375424432965, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92976, 'HP:0002832', 'Calcific stippling', 'XPO:0100081', 'abnormal anatomical entity in vitro', 0.5, 1.7901636446558942, 0.9460876398769551, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92977, 'HP:0002832', 'Calcific stippling', 'XPO:0100549', 'abnormal mitotic cell', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92978, 'HP:0002832', 'Calcific stippling', 'XPO:0101569', 'abnormal activin-induced ectoderm', 0.47368421052631576, 1.7901636446558942, 0.9208540887305324, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92979, 'HP:0002832', 'Calcific stippling', 'XPO:0100070', 'abnormal anatomical system', 0.42857142857142855, 1.7901636446558942, 0.8759069531444602, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92980, 'HP:0002832', 'Calcific stippling', 'XPO:0100557', 'abnormal prime meridian', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92981, 'HP:0002832', 'Calcific stippling', 'XPO:0141772', 'abnormal water homeostasis', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92982, 'HP:0002832', 'Calcific stippling', 'XPO:0115505', 'dead whole organism', 0.45, 1.7901636446558942, 0.8975375424432965, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92983, 'HP:0002832', 'Calcific stippling', 'XPO:0100585', 'abnormal elastica externa', 0.45454545454545453, 4.401455821078525, 1.414447502332227, 'UPHENO:0002964', 'abnormal skeletal system'),
(92984, 'HP:0002832', 'Calcific stippling', 'XPO:0100643', 'abnormal thoracic region', 0.42857142857142855, 1.7901636446558942, 0.8759069531444602, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92985, 'HP:0002832', 'Calcific stippling', 'XPO:0101570', 'abnormal forelimb region', 0.42857142857142855, 1.7901636446558942, 0.8759069531444602, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92986, 'HP:0002832', 'Calcific stippling', 'XPO:0100363', 'abnormal cardiovascular system', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92987, 'HP:0002832', 'Calcific stippling', 'XPO:0141738', 'abnormal carbon dioxide homeostasis', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92988, 'HP:0002832', 'Calcific stippling', 'XPO:0100781', 'abnormal presumptive ectoderm', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92989, 'HP:0002832', 'Calcific stippling', 'XPO:0107258', 'abnormal anatomical axis', 0.47368421052631576, 1.7901636446558942, 0.9208540887305324, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92990, 'HP:0002832', 'Calcific stippling', 'XPO:0101333', 'abnormal barrier epithelial cell', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92991, 'HP:0002832', 'Calcific stippling', 'XPO:0107267', 'abnormal ventral side', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92992, 'HP:0002832', 'Calcific stippling', 'XPO:0100394', 'abnormal marginal zone', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92993, 'HP:0002832', 'Calcific stippling', 'XPO:0131691', 'abnormal molecular function', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(92994, 'HP:0002832', 'Calcific stippling', 'XPO:0100728', 'abnormal cell condensation', 0.45, 1.7901636446558942, 0.8975375424432965, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92995, 'HP:0002832', 'Calcific stippling', 'XPO:0101326', 'abnormal cementoblast', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92996, 'HP:0002832', 'Calcific stippling', 'XPO:0141715', 'abnormal septum', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92997, 'HP:0002832', 'Calcific stippling', 'XPO:0100028', 'abnormal anatomical cluster', 0.42857142857142855, 1.7901636446558942, 0.8759069531444602, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92998, 'HP:0002832', 'Calcific stippling', 'XPO:0115508', 'abnormally peramorphic growth of whole organism', 0.45, 1.7901636446558942, 0.8975375424432965, 'UPHENO:0002536', 'abnormal anatomical entity'),
(92999, 'HP:0002832', 'Calcific stippling', 'XPO:0101157', 'abnormal female organism', 0.45, 1.7901636446558942, 0.8975375424432965, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93000, 'HP:0002832', 'Calcific stippling', 'XPO:0101519', 'abnormal hypobranchial placode', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93001, 'HP:0002832', 'Calcific stippling', 'XPO:0141266', 'abnormal surface breathing', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(93002, 'HP:0002832', 'Calcific stippling', 'XPO:0101503', 'abnormal organ cortex', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93003, 'HP:0002832', 'Calcific stippling', 'XPO:0107273', 'abnormal basal region', 0.42857142857142855, 1.7901636446558942, 0.8759069531444602, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93004, 'HP:0002832', 'Calcific stippling', 'XPO:0100969', 'abnormal disaggregated/reaggregated ectoderm treated with activin', 0.47368421052631576, 1.7901636446558942, 0.9208540887305324, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93005, 'HP:0002832', 'Calcific stippling', 'XPO:0100104', 'abnormal embryonic structure', 0.42857142857142855, 1.7901636446558942, 0.8759069531444602, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93006, 'HP:0002832', 'Calcific stippling', 'XPO:0101411', 'abnormal marginal zone (sensu neural)', 0.42857142857142855, 1.7901636446558942, 0.8759069531444602, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93007, 'HP:0002832', 'Calcific stippling', 'XPO:0100665', 'abnormal egg jelly', 0.42857142857142855, 1.7901636446558942, 0.8759069531444602, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93008, 'HP:0002832', 'Calcific stippling', 'XPO:0100003', 'abnormal organism subdivision', 0.42857142857142855, 1.7901636446558942, 0.8759069531444602, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93009, 'HP:0002832', 'Calcific stippling', 'XPO:0101373', 'abnormal oxygen accumulating cell', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93010, 'HP:0002832', 'Calcific stippling', 'XPO:0100384', 'abnormal amputated tissue', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93011, 'HP:0002832', 'Calcific stippling', 'XPO:0100009', 'abnormal multi-tissue structure', 0.42857142857142855, 1.7901636446558942, 0.8759069531444602, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93012, 'HP:0002832', 'Calcific stippling', 'XPO:0141263', 'abnormal visually guided collision avoidance behavior', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(93013, 'HP:0002832', 'Calcific stippling', 'XPO:0101004', 'abnormal acid secreting cell', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93014, 'HP:0002832', 'Calcific stippling', 'XPO:0141771', 'abnormal urea homeostasis', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(93015, 'HP:0002832', 'Calcific stippling', 'XPO:0100856', 'abnormal simple organ', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93016, 'HP:0002832', 'Calcific stippling', 'XPO:0100807', 'abnormal matrix-based tissue', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93017, 'HP:0002832', 'Calcific stippling', 'XPO:0101347', 'abnormal hindlimb region', 0.42857142857142855, 1.7901636446558942, 0.8759069531444602, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93018, 'HP:0002832', 'Calcific stippling', 'XPO:0100791', 'abnormal multiciliated cell precursor', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93019, 'HP:0002832', 'Calcific stippling', 'XPO:0107259', 'abnormal animal-vegetal axis', 0.45, 1.7901636446558942, 0.8975375424432965, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93020, 'HP:0002832', 'Calcific stippling', 'XPO:0100344', 'abnormal portion of organism substance', 0.5, 1.7901636446558942, 0.9460876398769551, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93021, 'HP:0002832', 'Calcific stippling', 'XPO:0141770', 'abnormal urate homeostasis', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(93022, 'HP:0002832', 'Calcific stippling', 'XPO:0107278', 'abnormal medial region', 0.42857142857142855, 1.7901636446558942, 0.8759069531444602, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93023, 'HP:0002832', 'Calcific stippling', 'XPO:0100006', 'abnormal anatomical structure', 0.5, 1.7901636446558942, 0.9460876398769551, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93024, 'HP:0002832', 'Calcific stippling', 'XPO:0100285', 'abnormal progenitor cell', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93025, 'HP:0002832', 'Calcific stippling', 'XPO:0100277', 'abnormal blastocoel', 0.42857142857142855, 1.7901636446558942, 0.8759069531444602, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93026, 'HP:0002832', 'Calcific stippling', 'XPO:0100004', 'abnormal cell', 0.42857142857142855, 1.7901636446558942, 0.8759069531444602, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93027, 'HP:0002832', 'Calcific stippling', 'XPO:0100108', 'abnormal cell part', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93028, 'HP:0002832', 'Calcific stippling', 'XPO:0107272', 'abnormal axial region', 0.42857142857142855, 1.7901636446558942, 0.8759069531444602, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93029, 'HP:0002832', 'Calcific stippling', 'XPO:0100239', 'abnormal acellular anatomical structure', 0.45, 1.7901636446558942, 0.8975375424432965, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93030, 'HP:0002832', 'Calcific stippling', 'XPO:0100573', 'abnormal extraembryonic structure', 0.45, 1.7901636446558942, 0.8975375424432965, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93031, 'HP:0002832', 'Calcific stippling', 'XPO:0101174', 'abnormal articular system', 0.4166666666666667, 4.401455821078525, 1.3542303812311203, 'UPHENO:0002964', 'abnormal skeletal system'),
(93032, 'HP:0002832', 'Calcific stippling', 'XPO:00000000', 'Xenopus phenotype', 0.47058823529411764, 1.6758249395539064, 0.8880447629295182, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(93033, 'HP:0002832', 'Calcific stippling', 'XPO:0100533', 'abnormal melanoblast', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93034, 'HP:0002832', 'Calcific stippling', 'XPO:0116434', 'abnormal biological process', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(93035, 'HP:0002832', 'Calcific stippling', 'XPO:0100481', 'abnormal anatomical line', 0.5, 1.7901636446558942, 0.9460876398769551, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93036, 'HP:0002832', 'Calcific stippling', 'XPO:0100084', 'abnormal anatomical group', 0.45, 1.7901636446558942, 0.8975375424432965, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93037, 'HP:0002832', 'Calcific stippling', 'XPO:0107266', 'abnormal dorsal side', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93038, 'HP:0002832', 'Calcific stippling', 'XPO:0100465', 'abnormal skeletal system', 0.43478260869565216, 4.401455821078525, 1.383356947409881, 'UPHENO:0002964', 'abnormal skeletal system'),
(93039, 'HP:0002832', 'Calcific stippling', 'XPO:0100640', 'abnormal notochordal sheath', 0.4166666666666667, 4.401455821078525, 1.3542303812311203, 'UPHENO:0002964', 'abnormal skeletal system'),
(93040, 'HP:0002832', 'Calcific stippling', 'XPO:0100258', 'abnormal organ part', 0.47368421052631576, 1.7901636446558942, 0.9208540887305324, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93041, 'HP:0002832', 'Calcific stippling', 'XPO:0101435', 'abnormal paracrine cell', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93042, 'HP:0002832', 'Calcific stippling', 'XPO:0131723', 'abnormal pathway-restricted SMAD protein phosphorylation', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(93043, 'HP:0002832', 'Calcific stippling', 'XPO:0131725', 'abnormal phosphorylation of RNA polymerase II C-terminal domain', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(93044, 'HP:0002832', 'Calcific stippling', 'XPO:0107276', 'abnormal dorsal region', 0.42857142857142855, 1.7901636446558942, 0.8759069531444602, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93045, 'HP:0002832', 'Calcific stippling', 'XPO:0141267', 'abnormal resting posture', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(93046, 'HP:0002832', 'Calcific stippling', 'XPO:0107261', 'abnormal dorsal-ventral axis', 0.45, 1.7901636446558942, 0.8975375424432965, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93047, 'HP:0002832', 'Calcific stippling', 'XPO:0100268', 'abnormal circulatory system', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93048, 'HP:0002832', 'Calcific stippling', 'XPO:0100151', 'abnormal primordium', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93049, 'HP:0002832', 'Calcific stippling', 'XPO:0100295', 'abnormal extracellular matrix', 0.42857142857142855, 1.7901636446558942, 0.8759069531444602, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93050, 'HP:0002832', 'Calcific stippling', 'XPO:0141315', 'abnormal anatomical region', 0.45, 1.7901636446558942, 0.8975375424432965, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93051, 'HP:0002832', 'Calcific stippling', 'XPO:0100786', 'abnormal presumptive axial mesoderm', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93052, 'HP:0002832', 'Calcific stippling', 'XPO:0101241', 'abnormal nucleate erythrocyte', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93053, 'HP:0002832', 'Calcific stippling', 'XPO:0141748', 'abnormal gas homeostasis', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(93054, 'HP:0002832', 'Calcific stippling', 'XPO:0141265', 'abnormal escape behavior', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(93055, 'HP:0002832', 'Calcific stippling', 'XPO:0141714', 'abnormal anterior notochord', 0.4166666666666667, 4.401455821078525, 1.3542303812311203, 'UPHENO:0002964', 'abnormal skeletal system'),
(93056, 'HP:0002832', 'Calcific stippling', 'XPO:0141272', 'absent surface breathing', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(93057, 'HP:0002832', 'Calcific stippling', 'XPO:0100546', 'abnormal whole organism', 0.47368421052631576, 1.7901636446558942, 0.9208540887305324, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93058, 'HP:0002832', 'Calcific stippling', 'XPO:0116494', 'absent biological process', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(93059, 'HP:0002832', 'Calcific stippling', 'XPO:0100915', 'abnormal dermal system', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93060, 'HP:0002832', 'Calcific stippling', 'XPO:0141271', 'increased surface breathing', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(93061, 'HP:0002832', 'Calcific stippling', 'XPO:0100691', 'abnormal keratin accumulating cell', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93062, 'HP:0002832', 'Calcific stippling', 'XPO:0100715', 'abnormal ciliated cell', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93063, 'HP:0002832', 'Calcific stippling', 'XPO:0101132', 'abnormal apoptotic cell', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93064, 'HP:0002832', 'Calcific stippling', 'XPO:0100026', 'abnormal germ cell', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93065, 'HP:0002832', 'Calcific stippling', 'XPO:0100477', 'abnormal pericyte', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93066, 'HP:0002832', 'Calcific stippling', 'XPO:0100913', 'abnormal Brachets cleft', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93067, 'HP:0002832', 'Calcific stippling', 'XPO:0100912', 'abnormal trabecula', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93068, 'HP:0002832', 'Calcific stippling', 'XPO:0100023', 'abnormal mesenchyme', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93069, 'HP:0002832', 'Calcific stippling', 'XPO:0141499', 'abnormal tadpole', 0.45, 1.7901636446558942, 0.8975375424432965, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93070, 'HP:0002832', 'Calcific stippling', 'XPO:0101200', 'abnormal joint region', 0.42857142857142855, 1.7901636446558942, 0.8759069531444602, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93071, 'HP:0002832', 'Calcific stippling', 'XPO:0100531', 'abnormal proliferative region', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93072, 'HP:0002832', 'Calcific stippling', 'XPO:0141264', 'abnormal schooling behavior', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(93073, 'HP:0002832', 'Calcific stippling', 'XPO:0100378', 'abnormal perichondrium', 0.4166666666666667, 4.401455821078525, 1.3542303812311203, 'UPHENO:0002964', 'abnormal skeletal system'),
(93074, 'HP:0002832', 'Calcific stippling', 'XPO:0101040', 'abnormal axial mesoderm', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93075, 'HP:0002832', 'Calcific stippling', 'XPO:0100545', 'abnormal male organism', 0.45, 1.7901636446558942, 0.8975375424432965, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93076, 'HP:0002832', 'Calcific stippling', 'XPO:0101467', 'abnormal alkali secreting cell', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93077, 'HP:0002832', 'Calcific stippling', 'XPO:0100339', 'abnormal circumblastoporal collar', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93078, 'HP:0002832', 'Calcific stippling', 'XPO:0107260', 'abnormal anterior-posterior axis', 0.45, 1.7901636446558942, 0.8975375424432965, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93079, 'HP:0002832', 'Calcific stippling', 'XPO:0100010', 'abnormal multicellular anatomical structure', 0.45, 1.7901636446558942, 0.8975375424432965, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93080, 'HP:0002832', 'Calcific stippling', 'XPO:0100251', 'abnormal proteinaceous extracellular matrix', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93081, 'HP:0002832', 'Calcific stippling', 'XPO:0100060', 'abnormal regenerating tissue', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93082, 'HP:0002832', 'Calcific stippling', 'XPO:0141276', 'decreased surface breathing', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(93083, 'HP:0002832', 'Calcific stippling', 'XPO:0100231', 'abnormal compound organ', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93084, 'HP:0002832', 'Calcific stippling', 'XPO:0107271', 'abnormal apical region', 0.42857142857142855, 1.7901636446558942, 0.8759069531444602, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93085, 'HP:0002832', 'Calcific stippling', 'XPO:0100192', 'abnormal epithelium', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93086, 'HP:0002832', 'Calcific stippling', 'XPO:0107268', 'abnormal left side', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93087, 'HP:0002832', 'Calcific stippling', 'XPO:0100762', 'abnormal intersomitic region', 0.42857142857142855, 1.7901636446558942, 0.8759069531444602, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93088, 'HP:0002832', 'Calcific stippling', 'XPO:0100337', 'abnormal zygote', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93089, 'HP:0002832', 'Calcific stippling', 'XPO:0100282', 'abnormal pelvic girdle primordium', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93090, 'HP:0002832', 'Calcific stippling', 'XPO:0107262', 'abnormal left-right axis', 0.45, 1.7901636446558942, 0.8975375424432965, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93091, 'HP:0002832', 'Calcific stippling', 'XPO:0141784', 'abnormal cellular hormone metabolic process', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(93092, 'HP:0002832', 'Calcific stippling', 'XPO:0100293', 'abnormal duct', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93093, 'HP:0002832', 'Calcific stippling', 'XPO:0100653', 'abnormal myoblast', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93094, 'HP:0002832', 'Calcific stippling', 'XPO:0100991', 'abnormal iliac process primordium', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93095, 'HP:0002832', 'Calcific stippling', 'XPO:0115512', 'abnormally semi-erect whole organism', 0.45, 1.7901636446558942, 0.8975375424432965, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93096, 'HP:0002832', 'Calcific stippling', 'XPO:0142056', 'abnormal main body axis', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93097, 'HP:0002832', 'Calcific stippling', 'XPO:0100610', 'abnormal appendage', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93098, 'HP:0002832', 'Calcific stippling', 'XPO:0101141', 'abnormal Keller explant', 0.47368421052631576, 1.7901636446558942, 0.9208540887305324, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93099, 'HP:0002832', 'Calcific stippling', 'XPO:0100704', 'abnormal Merkel cell', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93100, 'HP:0002832', 'Calcific stippling', 'XPO:0100423', 'abnormal process', 0.45, 1.7901636446558942, 0.8975375424432965, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93101, 'HP:0002832', 'Calcific stippling', 'XPO:0100062', 'abnormal anatomical space', 0.45, 1.7901636446558942, 0.8975375424432965, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93102, 'HP:0002832', 'Calcific stippling', 'XPO:0107285', 'abnormal flexural organ', 0.4166666666666667, 4.401455821078525, 1.3542303812311203, 'UPHENO:0002964', 'abnormal skeletal system'),
(93103, 'HP:0002832', 'Calcific stippling', 'XPO:0101448', 'abnormal myelin accumulating cell', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93104, 'HP:0002832', 'Calcific stippling', 'XPO:0100754', 'abnormal electrically active cell', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93105, 'HP:0002832', 'Calcific stippling', 'XPO:0141743', 'abnormal chemical homeostasis within a tissue', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(93106, 'HP:0002832', 'Calcific stippling', 'XPO:0107263', 'abnormal anatomical side', 0.42857142857142855, 1.7901636446558942, 0.8759069531444602, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93107, 'HP:0002832', 'Calcific stippling', 'XPO:0100135', 'abnormal surface structure', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93108, 'HP:0002832', 'Calcific stippling', 'XPO:0107264', 'abnormal anterior side', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93109, 'HP:0002832', 'Calcific stippling', 'XPO:0100162', 'abnormal presumptive rhombomere', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93110, 'HP:0002832', 'Calcific stippling', 'XPO:0107265', 'abnormal posterior side', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93111, 'HP:0002832', 'Calcific stippling', 'XPO:0100802', 'abnormal exocrine cell', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93112, 'HP:0002832', 'Calcific stippling', 'XPO:0100014', 'abnormal tissue', 0.42857142857142855, 1.7901636446558942, 0.8759069531444602, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93113, 'HP:0002832', 'Calcific stippling', 'XPO:0100667', 'abnormal vegetal yolk mass', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93114, 'HP:0002832', 'Calcific stippling', 'XPO:0100638', 'abnormal polar body', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93115, 'HP:0002832', 'Calcific stippling', 'XPO:0100422', 'abnormal notochord', 0.43478260869565216, 4.401455821078525, 1.383356947409881, 'UPHENO:0002964', 'abnormal skeletal system'),
(93116, 'HP:0002832', 'Calcific stippling', 'XPO:0101406', 'abnormal cleavage furrow', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93117, 'HP:0002832', 'Calcific stippling', 'XPO:0100852', 'abnormal interdigital region', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93118, 'HP:0002832', 'Calcific stippling', 'XPO:0107270', 'abnormal proximal-distal axis', 0.45, 1.7901636446558942, 0.8975375424432965, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93119, 'HP:0030061', 'Neuroectodermal neoplasm', 'XPO:0100545', 'abnormal male organism', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(93120, 'HP:0030061', 'Neuroectodermal neoplasm', 'XPO:0101569', 'abnormal activin-induced ectoderm', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(93121, 'HP:0030061', 'Neuroectodermal neoplasm', 'XPO:0131729', 'abnormal regulation of growth rate', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(93122, 'HP:0030061', 'Neuroectodermal neoplasm', 'XPO:0100081', 'abnormal anatomical entity in vitro', 0.47058823529411764, 1.6758249395539064, 0.8880447629295182, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(93123, 'HP:0030061', 'Neuroectodermal neoplasm', 'XPO:0141745', 'abnormal creatinine homeostasis', 0.5, 1.6758249395539064, 0.9153755894587495, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(93124, 'HP:0030061', 'Neuroectodermal neoplasm', 'XPO:0115505', 'dead whole organism', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(93125, 'HP:0030061', 'Neuroectodermal neoplasm', 'XPO:0141264', 'abnormal schooling behavior', 0.5, 1.6758249395539064, 0.9153755894587495, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(93126, 'HP:0030061', 'Neuroectodermal neoplasm', 'XPO:0100546', 'abnormal whole organism', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(93127, 'HP:0030061', 'Neuroectodermal neoplasm', 'XPO:0107260', 'abnormal anterior-posterior axis', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(93128, 'HP:0030061', 'Neuroectodermal neoplasm', 'XPO:0100423', 'abnormal process', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(93129, 'HP:0030061', 'Neuroectodermal neoplasm', 'XPO:0128000', 'absent behavior', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(93130, 'HP:0030061', 'Neuroectodermal neoplasm', 'XPO:0116494', 'absent biological process', 0.47058823529411764, 1.6758249395539064, 0.8880447629295182, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(93131, 'HP:0030061', 'Neuroectodermal neoplasm', 'XPO:00000000', 'Xenopus phenotype', 0.5333333333333333, 1.6758249395539064, 0.9453958435996092, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(93132, 'HP:0030061', 'Neuroectodermal neoplasm', 'XPO:0107258', 'abnormal anatomical axis', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(93133, 'HP:0030061', 'Neuroectodermal neoplasm', 'XPO:0100239', 'abnormal acellular anatomical structure', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(93134, 'HP:0030061', 'Neuroectodermal neoplasm', 'XPO:0107259', 'abnormal animal-vegetal axis', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(93135, 'HP:0030061', 'Neuroectodermal neoplasm', 'XPO:0141263', 'abnormal visually guided collision avoidance behavior', 0.5, 1.6758249395539064, 0.9153755894587495, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(93136, 'HP:0030061', 'Neuroectodermal neoplasm', 'XPO:0141499', 'abnormal tadpole', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(93137, 'HP:0030061', 'Neuroectodermal neoplasm', 'XPO:0131730', 'abnormal regulation of protein folding', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(93138, 'HP:0030061', 'Neuroectodermal neoplasm', 'XPO:0141315', 'abnormal anatomical region', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(93139, 'HP:0030061', 'Neuroectodermal neoplasm', 'XPO:0100006', 'abnormal anatomical structure', 0.47058823529411764, 1.6758249395539064, 0.8880447629295182, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(93140, 'HP:0030061', 'Neuroectodermal neoplasm', 'XPO:0141267', 'abnormal resting posture', 0.5, 1.6758249395539064, 0.9153755894587495, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(93141, 'HP:0030061', 'Neuroectodermal neoplasm', 'XPO:0101109', 'abnormal egg cell-free extract', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(93142, 'HP:0030061', 'Neuroectodermal neoplasm', 'XPO:0141600', 'absent metamorphosis', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(93143, 'HP:0030061', 'Neuroectodermal neoplasm', 'XPO:0116434', 'abnormal biological process', 0.47058823529411764, 1.6758249395539064, 0.8880447629295182, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(93144, 'HP:0030061', 'Neuroectodermal neoplasm', 'XPO:0141266', 'abnormal surface breathing', 0.5, 1.6758249395539064, 0.9153755894587495, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(93145, 'HP:0030061', 'Neuroectodermal neoplasm', 'XPO:0133388', 'absent insulin receptor signaling pathway', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(93146, 'HP:0030061', 'Neuroectodermal neoplasm', 'XPO:0107270', 'abnormal proximal-distal axis', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(93147, 'HP:0030061', 'Neuroectodermal neoplasm', 'XPO:0131723', 'abnormal pathway-restricted SMAD protein phosphorylation', 0.5, 1.6758249395539064, 0.9153755894587495, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(93148, 'HP:0030061', 'Neuroectodermal neoplasm', 'XPO:0141743', 'abnormal chemical homeostasis within a tissue', 0.5, 1.6758249395539064, 0.9153755894587495, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(93149, 'HP:0030061', 'Neuroectodermal neoplasm', 'XPO:0101141', 'abnormal Keller explant', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(93150, 'HP:0030061', 'Neuroectodermal neoplasm', 'XPO:0141271', 'increased surface breathing', 0.47058823529411764, 1.6758249395539064, 0.8880447629295182, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(93151, 'HP:0030061', 'Neuroectodermal neoplasm', 'XPO:0100010', 'abnormal multicellular anatomical structure', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(93152, 'HP:0030061', 'Neuroectodermal neoplasm', 'XPO:0133403', 'abnormal developmental process', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(93153, 'HP:0030061', 'Neuroectodermal neoplasm', 'XPO:0101110', 'abnormal cell-free extract', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(93154, 'HP:0030061', 'Neuroectodermal neoplasm', 'XPO:0100573', 'abnormal extraembryonic structure', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(93155, 'HP:0030061', 'Neuroectodermal neoplasm', 'XPO:0107262', 'abnormal left-right axis', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(93156, 'HP:0030061', 'Neuroectodermal neoplasm', 'XPO:0141776', 'abnormal metabolic process', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(93157, 'HP:0030061', 'Neuroectodermal neoplasm', 'XPO:0115509', 'abnormally semi-viable whole organism', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(93158, 'HP:0030061', 'Neuroectodermal neoplasm', 'XPO:0141265', 'abnormal escape behavior', 0.5, 1.6758249395539064, 0.9153755894587495, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(93159, 'HP:0030061', 'Neuroectodermal neoplasm', 'XPO:0100202', 'abnormal embryo', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(93160, 'HP:0030061', 'Neuroectodermal neoplasm', 'XPO:0141771', 'abnormal urea homeostasis', 0.5, 1.6758249395539064, 0.9153755894587495, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(93161, 'HP:0030061', 'Neuroectodermal neoplasm', 'XPO:0100728', 'abnormal cell condensation', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(93162, 'HP:0030061', 'Neuroectodermal neoplasm', 'XPO:0100481', 'abnormal anatomical line', 0.47058823529411764, 1.6758249395539064, 0.8880447629295182, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(93163, 'HP:0030061', 'Neuroectodermal neoplasm', 'XPO:0131469', 'abnormal heart process', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(93164, 'HP:0030061', 'Neuroectodermal neoplasm', 'XPO:0100084', 'abnormal anatomical group', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(93165, 'HP:0030061', 'Neuroectodermal neoplasm', 'XPO:0131691', 'abnormal molecular function', 0.47058823529411764, 1.6758249395539064, 0.8880447629295182, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(93166, 'HP:0030061', 'Neuroectodermal neoplasm', 'XPO:0107261', 'abnormal dorsal-ventral axis', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(93167, 'HP:0030061', 'Neuroectodermal neoplasm', 'XPO:0131725', 'abnormal phosphorylation of RNA polymerase II C-terminal domain', 0.5, 1.6758249395539064, 0.9153755894587495, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(93168, 'HP:0030061', 'Neuroectodermal neoplasm', 'XPO:0100344', 'abnormal portion of organism substance', 0.47058823529411764, 1.6758249395539064, 0.8880447629295182, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(93169, 'HP:0030061', 'Neuroectodermal neoplasm', 'XPO:0141772', 'abnormal water homeostasis', 0.5, 1.6758249395539064, 0.9153755894587495, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(93170, 'HP:0030061', 'Neuroectodermal neoplasm', 'XPO:0101157', 'abnormal female organism', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(93171, 'HP:0030061', 'Neuroectodermal neoplasm', 'XPO:0100969', 'abnormal disaggregated/reaggregated ectoderm treated with activin', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(93172, 'HP:0030061', 'Neuroectodermal neoplasm', 'XPO:0141748', 'abnormal gas homeostasis', 0.5, 1.6758249395539064, 0.9153755894587495, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(93173, 'HP:0030061', 'Neuroectodermal neoplasm', 'XPO:0141272', 'absent surface breathing', 0.5, 1.6758249395539064, 0.9153755894587495, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(93174, 'HP:0030061', 'Neuroectodermal neoplasm', 'XPO:0141809', 'abnormal catalytic activity', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(93175, 'HP:0030061', 'Neuroectodermal neoplasm', 'XPO:0141754', 'abnormal homeostatic process', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(93176, 'HP:0030061', 'Neuroectodermal neoplasm', 'XPO:0141276', 'decreased surface breathing', 0.47058823529411764, 1.6758249395539064, 0.8880447629295182, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(93177, 'HP:0030061', 'Neuroectodermal neoplasm', 'XPO:0141770', 'abnormal urate homeostasis', 0.5, 1.6758249395539064, 0.9153755894587495, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(93178, 'HP:0030061', 'Neuroectodermal neoplasm', 'XPO:0115508', 'abnormally peramorphic growth of whole organism', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(93179, 'HP:0030061', 'Neuroectodermal neoplasm', 'XPO:0100062', 'abnormal anatomical space', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(93180, 'HP:0030061', 'Neuroectodermal neoplasm', 'XPO:0115512', 'abnormally semi-erect whole organism', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(93181, 'HP:0030061', 'Neuroectodermal neoplasm', 'XPO:0141784', 'abnormal cellular hormone metabolic process', 0.5, 1.6758249395539064, 0.9153755894587495, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(93182, 'HP:0030061', 'Neuroectodermal neoplasm', 'XPO:0100258', 'abnormal organ part', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(93183, 'HP:0030061', 'Neuroectodermal neoplasm', 'XPO:0141738', 'abnormal carbon dioxide homeostasis', 0.5, 1.6758249395539064, 0.9153755894587495, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(93184, 'HP:0012545', 'Reduced circulating aldolase concentration', 'XPO:0141276', 'decreased surface breathing', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(93185, 'HP:0012545', 'Reduced circulating aldolase concentration', 'XPO:0131723', 'abnormal pathway-restricted SMAD protein phosphorylation', 0.47058823529411764, 1.6758249395539064, 0.8880447629295182, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(93186, 'HP:0012545', 'Reduced circulating aldolase concentration', 'XPO:0101141', 'abnormal Keller explant', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(93187, 'HP:0012545', 'Reduced circulating aldolase concentration', 'XPO:0116494', 'absent biological process', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(93188, 'HP:0012545', 'Reduced circulating aldolase concentration', 'XPO:0100546', 'abnormal whole organism', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(93189, 'HP:0012545', 'Reduced circulating aldolase concentration', 'XPO:0101110', 'abnormal cell-free extract', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(93190, 'HP:0012545', 'Reduced circulating aldolase concentration', 'XPO:0141772', 'abnormal water homeostasis', 0.47058823529411764, 1.6758249395539064, 0.8880447629295182, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(93191, 'HP:0012545', 'Reduced circulating aldolase concentration', 'XPO:0141265', 'abnormal escape behavior', 0.47058823529411764, 1.6758249395539064, 0.8880447629295182, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(93192, 'HP:0012545', 'Reduced circulating aldolase concentration', 'XPO:0101569', 'abnormal activin-induced ectoderm', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(93193, 'HP:0012545', 'Reduced circulating aldolase concentration', 'XPO:0100481', 'abnormal anatomical line', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(93194, 'HP:0012545', 'Reduced circulating aldolase concentration', 'XPO:0141784', 'abnormal cellular hormone metabolic process', 0.47058823529411764, 1.6758249395539064, 0.8880447629295182, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(93195, 'HP:0012545', 'Reduced circulating aldolase concentration', 'XPO:0116434', 'abnormal biological process', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(93196, 'HP:0012545', 'Reduced circulating aldolase concentration', 'XPO:0107258', 'abnormal anatomical axis', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(93197, 'HP:0012545', 'Reduced circulating aldolase concentration', 'XPO:0100344', 'abnormal portion of organism substance', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(93198, 'HP:0012545', 'Reduced circulating aldolase concentration', 'XPO:00000000', 'Xenopus phenotype', 0.5, 1.6758249395539064, 0.9153755894587495, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(93199, 'HP:0012545', 'Reduced circulating aldolase concentration', 'XPO:0141770', 'abnormal urate homeostasis', 0.47058823529411764, 1.6758249395539064, 0.8880447629295182, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(93200, 'HP:0012545', 'Reduced circulating aldolase concentration', 'XPO:0141771', 'abnormal urea homeostasis', 0.47058823529411764, 1.6758249395539064, 0.8880447629295182, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(93201, 'HP:0012545', 'Reduced circulating aldolase concentration', 'XPO:0141745', 'abnormal creatinine homeostasis', 0.47058823529411764, 1.6758249395539064, 0.8880447629295182, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(93202, 'HP:0012545', 'Reduced circulating aldolase concentration', 'XPO:0100969', 'abnormal disaggregated/reaggregated ectoderm treated with activin', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(93203, 'HP:0012545', 'Reduced circulating aldolase concentration', 'XPO:0131725', 'abnormal phosphorylation of RNA polymerase II C-terminal domain', 0.47058823529411764, 1.6758249395539064, 0.8880447629295182, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(93204, 'HP:0012545', 'Reduced circulating aldolase concentration', 'XPO:0141271', 'increased surface breathing', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(93205, 'HP:0012545', 'Reduced circulating aldolase concentration', 'XPO:0141266', 'abnormal surface breathing', 0.47058823529411764, 1.6758249395539064, 0.8880447629295182, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(93206, 'HP:0012545', 'Reduced circulating aldolase concentration', 'XPO:0141738', 'abnormal carbon dioxide homeostasis', 0.47058823529411764, 1.6758249395539064, 0.8880447629295182, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(93207, 'HP:0012545', 'Reduced circulating aldolase concentration', 'XPO:0141743', 'abnormal chemical homeostasis within a tissue', 0.47058823529411764, 1.6758249395539064, 0.8880447629295182, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(93208, 'HP:0012545', 'Reduced circulating aldolase concentration', 'XPO:0141264', 'abnormal schooling behavior', 0.47058823529411764, 1.6758249395539064, 0.8880447629295182, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(93209, 'HP:0012545', 'Reduced circulating aldolase concentration', 'XPO:0141272', 'absent surface breathing', 0.47058823529411764, 1.6758249395539064, 0.8880447629295182, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(93210, 'HP:0012545', 'Reduced circulating aldolase concentration', 'XPO:0100006', 'abnormal anatomical structure', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(93211, 'HP:0012545', 'Reduced circulating aldolase concentration', 'XPO:0141748', 'abnormal gas homeostasis', 0.47058823529411764, 1.6758249395539064, 0.8880447629295182, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(93212, 'HP:0012545', 'Reduced circulating aldolase concentration', 'XPO:0141263', 'abnormal visually guided collision avoidance behavior', 0.47058823529411764, 1.6758249395539064, 0.8880447629295182, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(93213, 'HP:0012545', 'Reduced circulating aldolase concentration', 'XPO:0141267', 'abnormal resting posture', 0.47058823529411764, 1.6758249395539064, 0.8880447629295182, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(93214, 'HP:0012545', 'Reduced circulating aldolase concentration', 'XPO:0100258', 'abnormal organ part', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(93215, 'HP:0012545', 'Reduced circulating aldolase concentration', 'XPO:0131691', 'abnormal molecular function', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(93216, 'HP:0012545', 'Reduced circulating aldolase concentration', 'XPO:0100081', 'abnormal anatomical entity in vitro', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(93217, 'HP:0031194', 'Increased density of left ventricular trabeculae', 'XPO:0102113', 'abnormal anatomical line morphology', 0.40625, 3.067140347159989, 1.1162552423320329, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(93218, 'HP:0031194', 'Increased density of left ventricular trabeculae', 'XPO:0101713', 'abnormal anatomical entity in vitro morphology', 0.40625, 3.067140347159989, 1.1162552423320329, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(93219, 'HP:0031194', 'Increased density of left ventricular trabeculae', 'XPO:0101638', 'abnormal anatomical structure morphology', 0.40625, 3.067140347159989, 1.1162552423320329, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(93220, 'HP:0031194', 'Increased density of left ventricular trabeculae', 'XPO:0101976', 'abnormal portion of organism substance morphology', 0.40625, 3.067140347159989, 1.1162552423320329, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(93221, 'HP:0031284', 'Flushing', 'XPO:0100481', 'abnormal anatomical line', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93222, 'HP:0031284', 'Flushing', 'XPO:0100344', 'abnormal portion of organism substance', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93223, 'HP:0031284', 'Flushing', 'XPO:0100006', 'abnormal anatomical structure', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93224, 'HP:0031284', 'Flushing', 'XPO:0100081', 'abnormal anatomical entity in vitro', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93225, 'HP:0004378', 'Abnormality of the anus', 'XPO:0141738', 'abnormal carbon dioxide homeostasis', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(93226, 'HP:0004378', 'Abnormality of the anus', 'XPO:0100152', 'abnormal alimentary system', 0.43478260869565216, 5.110459900932426, 1.4906170156555723, 'UPHENO:0002833', 'abnormal digestive system'),
(93227, 'HP:0004378', 'Abnormality of the anus', 'XPO:0100084', 'abnormal anatomical group', 0.42857142857142855, 1.7901636446558942, 0.8759069531444602, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93228, 'HP:0004378', 'Abnormality of the anus', 'XPO:0101411', 'abnormal marginal zone (sensu neural)', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93229, 'HP:0004378', 'Abnormality of the anus', 'XPO:0141263', 'abnormal visually guided collision avoidance behavior', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(93230, 'HP:0004378', 'Abnormality of the anus', 'XPO:0100009', 'abnormal multi-tissue structure', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93231, 'HP:0004378', 'Abnormality of the anus', 'XPO:0141265', 'abnormal escape behavior', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(93232, 'HP:0004378', 'Abnormality of the anus', 'XPO:0101200', 'abnormal joint region', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93233, 'HP:0004378', 'Abnormality of the anus', 'XPO:0100762', 'abnormal intersomitic region', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93234, 'HP:0004378', 'Abnormality of the anus', 'XPO:0115509', 'abnormally semi-viable whole organism', 0.42857142857142855, 1.7901636446558942, 0.8759069531444602, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93235, 'HP:0004378', 'Abnormality of the anus', 'XPO:0115512', 'abnormally semi-erect whole organism', 0.42857142857142855, 1.7901636446558942, 0.8759069531444602, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93236, 'HP:0004378', 'Abnormality of the anus', 'XPO:0115391', 'abnormally undifferentiated alimentary system', 0.4166666666666667, 5.110459900932426, 1.45923208985246, 'UPHENO:0002833', 'abnormal digestive system'),
(93237, 'HP:0004378', 'Abnormality of the anus', 'XPO:0100003', 'abnormal organism subdivision', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93238, 'HP:0004378', 'Abnormality of the anus', 'XPO:0100239', 'abnormal acellular anatomical structure', 0.42857142857142855, 1.7901636446558942, 0.8759069531444602, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93239, 'HP:0004378', 'Abnormality of the anus', 'XPO:0100070', 'abnormal anatomical system', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93240, 'HP:0004378', 'Abnormality of the anus', 'XPO:0101110', 'abnormal cell-free extract', 0.45, 1.7901636446558942, 0.8975375424432965, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93241, 'HP:0004378', 'Abnormality of the anus', 'XPO:0141266', 'abnormal surface breathing', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(93242, 'HP:0004378', 'Abnormality of the anus', 'XPO:0107259', 'abnormal animal-vegetal axis', 0.42857142857142855, 1.7901636446558942, 0.8759069531444602, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93243, 'HP:0004378', 'Abnormality of the anus', 'XPO:0100277', 'abnormal blastocoel', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93244, 'HP:0004378', 'Abnormality of the anus', 'XPO:0141264', 'abnormal schooling behavior', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(93245, 'HP:0004378', 'Abnormality of the anus', 'XPO:0101570', 'abnormal forelimb region', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93246, 'HP:0004378', 'Abnormality of the anus', 'XPO:0100423', 'abnormal process', 0.42857142857142855, 1.7901636446558942, 0.8759069531444602, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93247, 'HP:0004378', 'Abnormality of the anus', 'XPO:0100545', 'abnormal male organism', 0.42857142857142855, 1.7901636446558942, 0.8759069531444602, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93248, 'HP:0004378', 'Abnormality of the anus', 'XPO:0107278', 'abnormal medial region', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93249, 'HP:0004378', 'Abnormality of the anus', 'XPO:0100010', 'abnormal multicellular anatomical structure', 0.42857142857142855, 1.7901636446558942, 0.8759069531444602, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93250, 'HP:0004378', 'Abnormality of the anus', 'XPO:0100104', 'abnormal embryonic structure', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93251, 'HP:0004378', 'Abnormality of the anus', 'XPO:0141315', 'abnormal anatomical region', 0.42857142857142855, 1.7901636446558942, 0.8759069531444602, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93252, 'HP:0004378', 'Abnormality of the anus', 'XPO:0107262', 'abnormal left-right axis', 0.42857142857142855, 1.7901636446558942, 0.8759069531444602, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93253, 'HP:0004378', 'Abnormality of the anus', 'XPO:0141745', 'abnormal creatinine homeostasis', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(93254, 'HP:0004378', 'Abnormality of the anus', 'XPO:0107258', 'abnormal anatomical axis', 0.45, 1.7901636446558942, 0.8975375424432965, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93255, 'HP:0004378', 'Abnormality of the anus', 'XPO:0100202', 'abnormal embryo', 0.42857142857142855, 1.7901636446558942, 0.8759069531444602, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93256, 'HP:0004378', 'Abnormality of the anus', 'XPO:0141784', 'abnormal cellular hormone metabolic process', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(93257, 'HP:0004378', 'Abnormality of the anus', 'XPO:0115508', 'abnormally peramorphic growth of whole organism', 0.42857142857142855, 1.7901636446558942, 0.8759069531444602, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93258, 'HP:0004378', 'Abnormality of the anus', 'XPO:0107271', 'abnormal apical region', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93259, 'HP:0004378', 'Abnormality of the anus', 'XPO:0100295', 'abnormal extracellular matrix', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93260, 'HP:0004378', 'Abnormality of the anus', 'XPO:0100006', 'abnormal anatomical structure', 0.47368421052631576, 1.7901636446558942, 0.9208540887305324, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93261, 'HP:0004378', 'Abnormality of the anus', 'XPO:0141743', 'abnormal chemical homeostasis within a tissue', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(93262, 'HP:0004378', 'Abnormality of the anus', 'XPO:0141770', 'abnormal urate homeostasis', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(93263, 'HP:0004378', 'Abnormality of the anus', 'XPO:0141772', 'abnormal water homeostasis', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(93264, 'HP:0004378', 'Abnormality of the anus', 'XPO:0101109', 'abnormal egg cell-free extract', 0.42857142857142855, 1.7901636446558942, 0.8759069531444602, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93265, 'HP:0004378', 'Abnormality of the anus', 'XPO:0100004', 'abnormal cell', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93266, 'HP:0004378', 'Abnormality of the anus', 'XPO:0100258', 'abnormal organ part', 0.45, 1.7901636446558942, 0.8975375424432965, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93267, 'HP:0004378', 'Abnormality of the anus', 'XPO:0107270', 'abnormal proximal-distal axis', 0.42857142857142855, 1.7901636446558942, 0.8759069531444602, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93268, 'HP:0004378', 'Abnormality of the anus', 'XPO:0141272', 'absent surface breathing', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(93269, 'HP:0004378', 'Abnormality of the anus', 'XPO:0100481', 'abnormal anatomical line', 0.47368421052631576, 1.7901636446558942, 0.9208540887305324, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93270, 'HP:0004378', 'Abnormality of the anus', 'XPO:0100969', 'abnormal disaggregated/reaggregated ectoderm treated with activin', 0.45, 1.7901636446558942, 0.8975375424432965, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93271, 'HP:0004378', 'Abnormality of the anus', 'XPO:0141499', 'abnormal tadpole', 0.42857142857142855, 1.7901636446558942, 0.8759069531444602, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93272, 'HP:0004378', 'Abnormality of the anus', 'XPO:0100493', 'abnormal liver and biliary system', 0.4166666666666667, 5.110459900932426, 1.45923208985246, 'UPHENO:0002833', 'abnormal digestive system'),
(93273, 'HP:0004378', 'Abnormality of the anus', 'XPO:0100643', 'abnormal thoracic region', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93274, 'HP:0004378', 'Abnormality of the anus', 'XPO:0101569', 'abnormal activin-induced ectoderm', 0.45, 1.7901636446558942, 0.8975375424432965, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93275, 'HP:0004378', 'Abnormality of the anus', 'XPO:0100573', 'abnormal extraembryonic structure', 0.42857142857142855, 1.7901636446558942, 0.8759069531444602, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93276, 'HP:0004378', 'Abnormality of the anus', 'XPO:0100062', 'abnormal anatomical space', 0.42857142857142855, 1.7901636446558942, 0.8759069531444602, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93277, 'HP:0004378', 'Abnormality of the anus', 'XPO:0100028', 'abnormal anatomical cluster', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93278, 'HP:0004378', 'Abnormality of the anus', 'XPO:0131725', 'abnormal phosphorylation of RNA polymerase II C-terminal domain', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(93279, 'HP:0004378', 'Abnormality of the anus', 'XPO:0100081', 'abnormal anatomical entity in vitro', 0.47368421052631576, 1.7901636446558942, 0.9208540887305324, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93280, 'HP:0004378', 'Abnormality of the anus', 'XPO:0100546', 'abnormal whole organism', 0.45, 1.7901636446558942, 0.8975375424432965, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93281, 'HP:0004378', 'Abnormality of the anus', 'XPO:0107260', 'abnormal anterior-posterior axis', 0.42857142857142855, 1.7901636446558942, 0.8759069531444602, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93282, 'HP:0004378', 'Abnormality of the anus', 'XPO:0107288', 'abnormal larval alimentary system', 0.4166666666666667, 5.110459900932426, 1.45923208985246, 'UPHENO:0002833', 'abnormal digestive system'),
(93283, 'HP:0004378', 'Abnormality of the anus', 'XPO:0107261', 'abnormal dorsal-ventral axis', 0.42857142857142855, 1.7901636446558942, 0.8759069531444602, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93284, 'HP:0004378', 'Abnormality of the anus', 'XPO:0107276', 'abnormal dorsal region', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93285, 'HP:0004378', 'Abnormality of the anus', 'XPO:0107263', 'abnormal anatomical side', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93286, 'HP:0004378', 'Abnormality of the anus', 'XPO:0141771', 'abnormal urea homeostasis', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(93287, 'HP:0004378', 'Abnormality of the anus', 'XPO:0101141', 'abnormal Keller explant', 0.45, 1.7901636446558942, 0.8975375424432965, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93288, 'HP:0004378', 'Abnormality of the anus', 'XPO:0101157', 'abnormal female organism', 0.42857142857142855, 1.7901636446558942, 0.8759069531444602, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93289, 'HP:0004378', 'Abnormality of the anus', 'XPO:0101347', 'abnormal hindlimb region', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93290, 'HP:0004378', 'Abnormality of the anus', 'XPO:0107272', 'abnormal axial region', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93291, 'HP:0004378', 'Abnormality of the anus', 'XPO:0100344', 'abnormal portion of organism substance', 0.47368421052631576, 1.7901636446558942, 0.9208540887305324, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93292, 'HP:0004378', 'Abnormality of the anus', 'XPO:0107273', 'abnormal basal region', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93293, 'HP:0004378', 'Abnormality of the anus', 'XPO:0141748', 'abnormal gas homeostasis', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(93294, 'HP:0004378', 'Abnormality of the anus', 'XPO:0100665', 'abnormal egg jelly', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93295, 'HP:0004378', 'Abnormality of the anus', 'XPO:0115505', 'dead whole organism', 0.42857142857142855, 1.7901636446558942, 0.8759069531444602, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93296, 'HP:0004378', 'Abnormality of the anus', 'XPO:0141267', 'abnormal resting posture', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(93297, 'HP:0004378', 'Abnormality of the anus', 'XPO:0131723', 'abnormal pathway-restricted SMAD protein phosphorylation', 0.42105263157894735, 1.6758249395539064, 0.8400062504915083, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(93298, 'HP:0004378', 'Abnormality of the anus', 'XPO:0100014', 'abnormal tissue', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93299, 'HP:0004378', 'Abnormality of the anus', 'XPO:0100728', 'abnormal cell condensation', 0.42857142857142855, 1.7901636446558942, 0.8759069531444602, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93300, 'HP:0004378', 'Abnormality of the anus', 'XPO:00000000', 'Xenopus phenotype', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(93301, 'HP:0033312', 'Abnormal Bowman space morphology', 'XPO:0101717', 'abnormal mesonephric sinus morphology', 0.41304347826086957, 7.667568053596582, 1.7796176495695522, 'UPHENO:0076779', 'abnormal kidney morphology'),
(93302, 'HP:0000068', 'Urethral atresia', 'XPO:0103211', 'abnormal urethra morphology', 0.4318181818181818, 11.92532322793753, 2.26926670840651, 'UPHENO:0087871', 'abnormal urethra morphology'),
(93303, 'HP:0000275', 'Narrow face', 'XPO:0103358', 'decreased size of the pharyngeal region', 0.4166666666666667, 5.658780036326598, 1.5355210891212412, 'UPHENO:0012541', 'decreased size of the anatomical entity in the independent continuant'),
(93304, 'HP:0011742', 'Ectopic adrenal gland', 'XPO:0102722', 'abnormal adrenal gland morphology', 0.40816326530612246, 12.732678149995134, 2.279695481811975, 'UPHENO:0020671', 'abnormal adrenal gland morphology'),
(93305, 'HP:0030451', 'Mesenteric cyst', 'XPO:0115510', 'abnormal degeneration of whole organism', 0.4482758620689655, 3.067140347159989, 1.1725719522526752, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(93306, 'HP:0030451', 'Mesenteric cyst', 'XPO:0101834', 'abnormal embryo morphology', 0.41935483870967744, 3.067140347159989, 1.134116460326373, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(93307, 'HP:0030451', 'Mesenteric cyst', 'XPO:0103201', 'abnormal activin-induced ectoderm morphology', 0.4642857142857143, 3.067140347159989, 1.1933270494276536, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(93308, 'HP:0030451', 'Mesenteric cyst', 'XPO:0140284', 'abnormally necrotic dorsal region', 0.40625, 3.067140347159989, 1.1162552423320329, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(93309, 'HP:0030451', 'Mesenteric cyst', 'XPO:0101635', 'abnormal organism subdivision morphology', 0.41935483870967744, 3.067140347159989, 1.134116460326373, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(93310, 'HP:0030451', 'Mesenteric cyst', 'XPO:0102360', 'abnormal cell condensation morphology', 0.4482758620689655, 3.067140347159989, 1.1725719522526752, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(93311, 'HP:0030451', 'Mesenteric cyst', 'XPO:0107352', 'abnormal posterior side morphology', 0.40625, 3.067140347159989, 1.1162552423320329, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(93312, 'HP:0030451', 'Mesenteric cyst', 'XPO:0102601', 'abnormal disaggregated/reaggregated ectoderm treated with activin morphology', 0.4642857142857143, 3.067140347159989, 1.1933270494276536, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(93313, 'HP:0030451', 'Mesenteric cyst', 'XPO:0101660', 'abnormal anatomical cluster morphology', 0.41935483870967744, 3.067140347159989, 1.134116460326373, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(93314, 'HP:0030451', 'Mesenteric cyst', 'XPO:0140566', 'abnormally necrotic apical region', 0.40625, 3.067140347159989, 1.1162552423320329, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(93315, 'HP:0030451', 'Mesenteric cyst', 'XPO:0102113', 'abnormal anatomical line morphology', 0.5, 3.067140347159989, 1.2383740039180386, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(93316, 'HP:0030451', 'Mesenteric cyst', 'XPO:0140179', 'abnormally necrotic postero-dorsal region', 0.41935483870967744, 3.067140347159989, 1.134116460326373, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(93317, 'HP:0030451', 'Mesenteric cyst', 'XPO:0101909', 'abnormal blastocoel morphology', 0.41935483870967744, 3.067140347159989, 1.134116460326373, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(93318, 'HP:0030451', 'Mesenteric cyst', 'XPO:0107355', 'abnormal left side morphology', 0.40625, 3.067140347159989, 1.1162552423320329, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(93319, 'HP:0030451', 'Mesenteric cyst', 'XPO:0128037', 'decreased size of the anatomical space', 0.40625, 3.067140347159989, 1.1162552423320329, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(93320, 'HP:0030451', 'Mesenteric cyst', 'XPO:0107349', 'abnormal left-right axis morphology', 0.43333333333333335, 3.067140347159989, 1.1528634569783167, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(93321, 'HP:0030451', 'Mesenteric cyst', 'XPO:0129517', 'increased size of the anatomical space', 0.40625, 3.067140347159989, 1.1162552423320329, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(93322, 'HP:0030451', 'Mesenteric cyst', 'XPO:0139886', 'abnormally necrotic process', 0.40625, 3.067140347159989, 1.1162552423320329, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(93323, 'HP:0030451', 'Mesenteric cyst', 'XPO:0139713', 'abnormally necrotic multicellular anatomical structure', 0.40625, 3.067140347159989, 1.1162552423320329, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(93324, 'HP:0030451', 'Mesenteric cyst', 'XPO:0140052', 'abnormally necrotic organ part', 0.41935483870967744, 3.067140347159989, 1.134116460326373, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(93325, 'HP:0030451', 'Mesenteric cyst', 'XPO:0101716', 'abnormal anatomical group morphology', 0.4482758620689655, 3.067140347159989, 1.1725719522526752, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(93326, 'HP:0030451', 'Mesenteric cyst', 'XPO:0101871', 'abnormal acellular anatomical structure morphology', 0.4482758620689655, 3.067140347159989, 1.1725719522526752, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(93327, 'HP:0030451', 'Mesenteric cyst', 'XPO:0107348', 'abnormal dorsal-ventral axis morphology', 0.43333333333333335, 3.067140347159989, 1.1528634569783167, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(93328, 'HP:0030451', 'Mesenteric cyst', 'XPO:0140395', 'abnormally necrotic antero-dorsal region', 0.41935483870967744, 3.067140347159989, 1.134116460326373, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(93329, 'HP:0030451', 'Mesenteric cyst', 'XPO:0140927', 'abnormally necrotic basal region', 0.40625, 3.067140347159989, 1.1162552423320329, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(93330, 'HP:0030451', 'Mesenteric cyst', 'XPO:0101638', 'abnormal anatomical structure morphology', 0.5, 3.067140347159989, 1.2383740039180386, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(93331, 'HP:0030451', 'Mesenteric cyst', 'XPO:0102789', 'abnormal female organism morphology', 0.43333333333333335, 3.067140347159989, 1.1528634569783167, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(93332, 'HP:0030451', 'Mesenteric cyst', 'XPO:0129487', 'increased size of the anatomical structure', 0.43333333333333335, 3.067140347159989, 1.1528634569783167, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(93333, 'HP:0030451', 'Mesenteric cyst', 'XPO:0107357', 'abnormal proximal-distal axis morphology', 0.43333333333333335, 3.067140347159989, 1.1528634569783167, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(93334, 'HP:0030451', 'Mesenteric cyst', 'XPO:0139763', 'abnormally necrotic anatomical group', 0.40625, 3.067140347159989, 1.1162552423320329, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(93335, 'HP:0030451', 'Mesenteric cyst', 'XPO:0140955', 'abnormally necrotic ventro-lateral region', 0.41935483870967744, 3.067140347159989, 1.134116460326373, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(93336, 'HP:0030451', 'Mesenteric cyst', 'XPO:0140269', 'abnormally necrotic anatomical line', 0.4642857142857143, 3.067140347159989, 1.1933270494276536, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(93337, 'HP:0030451', 'Mesenteric cyst', 'XPO:0107353', 'abnormal dorsal side morphology', 0.40625, 3.067140347159989, 1.1162552423320329, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(93338, 'HP:0030451', 'Mesenteric cyst', 'XPO:0128502', 'decreased size of the anatomical line', 0.43333333333333335, 3.067140347159989, 1.1528634569783167, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(93339, 'HP:0030451', 'Mesenteric cyst', 'XPO:0102205', 'abnormal extraembryonic structure morphology', 0.43333333333333335, 3.067140347159989, 1.1528634569783167, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(93340, 'HP:0030451', 'Mesenteric cyst', 'XPO:0107356', 'abnormal right side morphology', 0.40625, 3.067140347159989, 1.1162552423320329, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(93341, 'HP:0030451', 'Mesenteric cyst', 'XPO:0102742', 'abnormal cell-free extract morphology', 0.4642857142857143, 3.067140347159989, 1.1933270494276536, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(93342, 'HP:0030451', 'Mesenteric cyst', 'XPO:0140144', 'abnormally necrotic portion of organism substance', 0.4642857142857143, 3.067140347159989, 1.1933270494276536, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(93343, 'HP:0030451', 'Mesenteric cyst', 'XPO:0101890', 'abnormal organ part morphology', 0.4642857142857143, 3.067140347159989, 1.1933270494276536, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(93344, 'HP:0030451', 'Mesenteric cyst', 'XPO:0139841', 'abnormally necrotic anatomical region', 0.43333333333333335, 3.067140347159989, 1.1528634569783167, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(93345, 'HP:0030451', 'Mesenteric cyst', 'XPO:0107351', 'abnormal anterior side morphology', 0.40625, 3.067140347159989, 1.1162552423320329, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(93346, 'HP:0030451', 'Mesenteric cyst', 'XPO:0139718', 'abnormally necrotic anatomical structure', 0.4642857142857143, 3.067140347159989, 1.1933270494276536, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(93347, 'HP:0030451', 'Mesenteric cyst', 'XPO:0101740', 'abnormal cell part morphology', 0.41935483870967744, 3.067140347159989, 1.134116460326373, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(93348, 'HP:0030451', 'Mesenteric cyst', 'XPO:0140167', 'abnormally necrotic medial region', 0.40625, 3.067140347159989, 1.1162552423320329, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(93349, 'HP:0030451', 'Mesenteric cyst', 'XPO:0101636', 'abnormal cell morphology', 0.41935483870967744, 3.067140347159989, 1.134116460326373, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(93350, 'HP:0030451', 'Mesenteric cyst', 'XPO:0101646', 'abnormal tissue morphology', 0.41935483870967744, 3.067140347159989, 1.134116460326373, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(93351, 'HP:0030451', 'Mesenteric cyst', 'XPO:0140373', 'abnormally necrotic whole organism', 0.41935483870967744, 3.067140347159989, 1.134116460326373, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(93352, 'HP:0030451', 'Mesenteric cyst', 'XPO:0102773', 'abnormal Keller explant morphology', 0.4642857142857143, 3.067140347159989, 1.1933270494276536, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(93353, 'HP:0030451', 'Mesenteric cyst', 'XPO:0102177', 'abnormal male organism morphology', 0.43333333333333335, 3.067140347159989, 1.1528634569783167, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(93354, 'HP:0030451', 'Mesenteric cyst', 'XPO:0102189', 'abnormal prime meridian morphology', 0.40625, 3.067140347159989, 1.1162552423320329, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(93355, 'HP:0030451', 'Mesenteric cyst', 'XPO:0140567', 'abnormally necrotic postero-ventral region', 0.41935483870967744, 3.067140347159989, 1.134116460326373, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(93356, 'HP:0030451', 'Mesenteric cyst', 'XPO:0101713', 'abnormal anatomical entity in vitro morphology', 0.5, 3.067140347159989, 1.2383740039180386, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(93357, 'HP:0030451', 'Mesenteric cyst', 'XPO:0141189', 'abnormally necrotic antero-ventral region', 0.41935483870967744, 3.067140347159989, 1.134116460326373, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(93358, 'HP:0030451', 'Mesenteric cyst', 'XPO:0102275', 'abnormal thoracic region morphology', 0.43333333333333335, 3.067140347159989, 1.1528634569783167, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(93359, 'HP:0030451', 'Mesenteric cyst', 'XPO:0102055', 'abnormal process morphology', 0.4482758620689655, 3.067140347159989, 1.1725719522526752, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(93360, 'HP:0030451', 'Mesenteric cyst', 'XPO:0141334', 'increased pigmentation in the whole organism', 0.41935483870967744, 3.067140347159989, 1.134116460326373, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(93361, 'HP:0030451', 'Mesenteric cyst', 'XPO:0101784', 'abnormal alimentary system morphology', 0.4117647058823529, 5.110459900932426, 1.4506229758386564, 'UPHENO:0002833', 'abnormal digestive system'),
(93362, 'HP:0030451', 'Mesenteric cyst', 'XPO:0129982', 'increased size of the anatomical line', 0.43333333333333335, 3.067140347159989, 1.1528634569783167, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(93363, 'HP:0030451', 'Mesenteric cyst', 'XPO:0102741', 'abnormal egg cell-free extract morphology', 0.43333333333333335, 3.067140347159989, 1.1528634569783167, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(93364, 'HP:0030451', 'Mesenteric cyst', 'XPO:0141316', 'abnormal anatomical region morphology', 0.4642857142857143, 3.067140347159989, 1.1933270494276536, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(93365, 'HP:0030451', 'Mesenteric cyst', 'XPO:0102178', 'abnormal whole organism morphology', 0.4642857142857143, 3.067140347159989, 1.1933270494276536, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(93366, 'HP:0030451', 'Mesenteric cyst', 'XPO:0141254', 'abnormally necrotic dorso-lateral region', 0.41935483870967744, 3.067140347159989, 1.134116460326373, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(93367, 'HP:0030451', 'Mesenteric cyst', 'XPO:0141165', 'abnormally necrotic ventral region', 0.41935483870967744, 3.067140347159989, 1.134116460326373, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(93368, 'HP:0030451', 'Mesenteric cyst', 'XPO:0103043', 'abnormal marginal zone (sensu neural) morphology', 0.43333333333333335, 3.067140347159989, 1.1528634569783167, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(93369, 'HP:0030451', 'Mesenteric cyst', 'XPO:0128007', 'decreased size of the anatomical structure', 0.43333333333333335, 3.067140347159989, 1.1528634569783167, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(93370, 'HP:0030451', 'Mesenteric cyst', 'XPO:0102297', 'abnormal egg jelly morphology', 0.41935483870967744, 3.067140347159989, 1.134116460326373, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(93371, 'HP:0030451', 'Mesenteric cyst', 'XPO:0141505', 'abnormal tadpole morphology', 0.43333333333333335, 3.067140347159989, 1.1528634569783167, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(93372, 'HP:0030451', 'Mesenteric cyst', 'XPO:0102522', 'abnormal pharyngeal cavity morphology', 0.4117647058823529, 5.110459900932426, 1.4506229758386564, 'UPHENO:0002833', 'abnormal digestive system'),
(93373, 'HP:0030451', 'Mesenteric cyst', 'XPO:0107359', 'abnormal axial region morphology', 0.43333333333333335, 3.067140347159989, 1.1528634569783167, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(93374, 'HP:0030451', 'Mesenteric cyst', 'XPO:0102394', 'abnormal intersomitic region morphology', 0.40625, 3.067140347159989, 1.1162552423320329, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(93375, 'HP:0030451', 'Mesenteric cyst', 'XPO:0140389', 'abnormally necrotic cell condensation', 0.40625, 3.067140347159989, 1.1162552423320329, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(93376, 'HP:0030451', 'Mesenteric cyst', 'XPO:0107347', 'abnormal anterior-posterior axis morphology', 0.43333333333333335, 3.067140347159989, 1.1528634569783167, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(93377, 'HP:0030451', 'Mesenteric cyst', 'XPO:0128102', 'decreased size of the portion of organism substance', 0.43333333333333335, 3.067140347159989, 1.1528634569783167, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(93378, 'HP:0030451', 'Mesenteric cyst', 'XPO:0102979', 'abnormal hindlimb region morphology', 0.43333333333333335, 3.067140347159989, 1.1528634569783167, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(93379, 'HP:0030451', 'Mesenteric cyst', 'XPO:0107346', 'abnormal animal-vegetal axis morphology', 0.43333333333333335, 3.067140347159989, 1.1528634569783167, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(93380, 'HP:0030451', 'Mesenteric cyst', 'XPO:0129582', 'increased size of the portion of organism substance', 0.43333333333333335, 3.067140347159989, 1.1528634569783167, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(93381, 'HP:0030451', 'Mesenteric cyst', 'XPO:0101642', 'abnormal multicellular anatomical structure morphology', 0.4482758620689655, 3.067140347159989, 1.1725719522526752, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(93382, 'HP:0030451', 'Mesenteric cyst', 'XPO:0139923', 'abnormally necrotic acellular anatomical structure', 0.40625, 3.067140347159989, 1.1162552423320329, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(93383, 'HP:0030451', 'Mesenteric cyst', 'XPO:0107345', 'abnormal anatomical axis morphology', 0.4642857142857143, 3.067140347159989, 1.1933270494276536, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(93384, 'HP:0030451', 'Mesenteric cyst', 'XPO:0101702', 'abnormal anatomical system morphology', 0.41935483870967744, 3.067140347159989, 1.134116460326373, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(93385, 'HP:0030451', 'Mesenteric cyst', 'XPO:0140364', 'abnormally necrotic anterior region', 0.41935483870967744, 3.067140347159989, 1.134116460326373, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(93386, 'HP:0030451', 'Mesenteric cyst', 'XPO:0141091', 'abnormally necrotic posterior region', 0.41935483870967744, 3.067140347159989, 1.134116460326373, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(93387, 'HP:0030451', 'Mesenteric cyst', 'XPO:0102832', 'abnormal joint region morphology', 0.43333333333333335, 3.067140347159989, 1.1528634569783167, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(93388, 'HP:0030451', 'Mesenteric cyst', 'XPO:0101736', 'abnormal embryonic structure morphology', 0.41935483870967744, 3.067140347159989, 1.134116460326373, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(93389, 'HP:0030451', 'Mesenteric cyst', 'XPO:0107350', 'abnormal anatomical side morphology', 0.43333333333333335, 3.067140347159989, 1.1528634569783167, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(93390, 'HP:0030451', 'Mesenteric cyst', 'XPO:0103202', 'abnormal forelimb region morphology', 0.43333333333333335, 3.067140347159989, 1.1528634569783167, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(93391, 'HP:0030451', 'Mesenteric cyst', 'XPO:0107354', 'abnormal ventral side morphology', 0.40625, 3.067140347159989, 1.1162552423320329, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(93392, 'HP:0030451', 'Mesenteric cyst', 'XPO:0128091', 'decreased size of the anatomical region', 0.40625, 3.067140347159989, 1.1162552423320329, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(93393, 'HP:0030451', 'Mesenteric cyst', 'XPO:0129571', 'increased size of the anatomical region', 0.40625, 3.067140347159989, 1.1162552423320329, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(93394, 'HP:0030451', 'Mesenteric cyst', 'XPO:0101927', 'abnormal extracellular matrix morphology', 0.41935483870967744, 3.067140347159989, 1.134116460326373, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(93395, 'HP:0030451', 'Mesenteric cyst', 'XPO:0103927', 'decreased pigmentation in the whole organism', 0.41935483870967744, 3.067140347159989, 1.134116460326373, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(93396, 'HP:0030451', 'Mesenteric cyst', 'XPO:0101976', 'abnormal portion of organism substance morphology', 0.5, 3.067140347159989, 1.2383740039180386, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(93397, 'HP:0030451', 'Mesenteric cyst', 'XPO:0101694', 'abnormal anatomical space morphology', 0.4642857142857143, 3.067140347159989, 1.1933270494276536, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(93398, 'HP:0030451', 'Mesenteric cyst', 'XPO:0101641', 'abnormal multi-tissue structure morphology', 0.41935483870967744, 3.067140347159989, 1.134116460326373, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(93399, 'HP:0005587', 'Profuse pigmented skin lesions', 'XPO:0100344', 'abnormal portion of organism substance', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93400, 'HP:0005587', 'Profuse pigmented skin lesions', 'XPO:0100006', 'abnormal anatomical structure', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93401, 'HP:0005587', 'Profuse pigmented skin lesions', 'XPO:0100081', 'abnormal anatomical entity in vitro', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93402, 'HP:0005587', 'Profuse pigmented skin lesions', 'XPO:0100481', 'abnormal anatomical line', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93403, 'HP:0040248', 'Reduced plasminogen activator inhibitor 1 activity', 'XPO:0141272', 'absent surface breathing', 0.4444444444444444, 1.6758249395539064, 0.8630243821852199, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(93404, 'HP:0040248', 'Reduced plasminogen activator inhibitor 1 activity', 'XPO:0100781', 'abnormal presumptive ectoderm', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93405, 'HP:0040248', 'Reduced plasminogen activator inhibitor 1 activity', 'XPO:0101157', 'abnormal female organism', 0.45, 1.7901636446558942, 0.8975375424432965, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93406, 'HP:0040248', 'Reduced plasminogen activator inhibitor 1 activity', 'XPO:0107267', 'abnormal ventral side', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93407, 'HP:0040248', 'Reduced plasminogen activator inhibitor 1 activity', 'XPO:0100728', 'abnormal cell condensation', 0.45, 1.7901636446558942, 0.8975375424432965, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93408, 'HP:0040248', 'Reduced plasminogen activator inhibitor 1 activity', 'XPO:0100010', 'abnormal multicellular anatomical structure', 0.45, 1.7901636446558942, 0.8975375424432965, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93409, 'HP:0040248', 'Reduced plasminogen activator inhibitor 1 activity', 'XPO:0100268', 'abnormal circulatory system', 0.4090909090909091, 1.7901636446558942, 0.8557684691631112, 'UPHENO:0002536', 'abnormal anatomical entity'),
(93410, 'HP:0040248', 'Reduced plasminogen activator inhibitor 1 activity', 'XPO:0101200', 'abnormal joint region', 0.42857142857142855, 1.7901636446558942, 0.8759069531444602, 'UPHENO:0002536', 'abnormal anatomical entity'),
