(21254, 'HP:0003837', 'Soft-tissue ossification around the shoulders', 'XPO:0141091', 'abnormally necrotic posterior region', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(21255, 'HP:0003837', 'Soft-tissue ossification around the shoulders', 'XPO:0102275', 'abnormal thoracic region morphology', 0.41935483870967744, 2.786899518863159, 1.0810641970914296, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(21256, 'HP:0003837', 'Soft-tissue ossification around the shoulders', 'XPO:0102768', 'abnormal ooplasm morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(21257, 'HP:0003837', 'Soft-tissue ossification around the shoulders', 'XPO:0141699', 'abnormally necrotic anterior notochord', 0.47619047619047616, 4.638757693672553, 1.4862477031377266, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(21258, 'HP:0003837', 'Soft-tissue ossification around the shoulders', 'XPO:0139841', 'abnormally necrotic anatomical region', 0.41935483870967744, 2.786899518863159, 1.0810641970914296, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(21259, 'HP:0003837', 'Soft-tissue ossification around the shoulders', 'XPO:0100465', 'abnormal skeletal system', 0.45161290322580644, 4.3395673355180735, 1.399930213666808, 'UPHENO:0002964', 'abnormal skeletal system'),
(21260, 'HP:0003837', 'Soft-tissue ossification around the shoulders', 'XPO:0140432', 'abnormally necrotic skeleton', 0.47619047619047616, 4.638757693672553, 1.4862477031377266, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(21261, 'HP:0003837', 'Soft-tissue ossification around the shoulders', 'XPO:0141289', 'abnormal spindle microtubule morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(21262, 'HP:0003837', 'Soft-tissue ossification around the shoulders', 'XPO:0102789', 'abnormal female organism morphology', 0.41935483870967744, 2.786899518863159, 1.0810641970914296, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(21263, 'HP:0003837', 'Soft-tissue ossification around the shoulders', 'XPO:0102588', 'abnormal centrosome morphology', 0.42857142857142855, 2.786899518863159, 1.092879457252359, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(21264, 'HP:0003837', 'Soft-tissue ossification around the shoulders', 'XPO:0101681', 'abnormal chondrocranium morphology', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(21265, 'HP:0003837', 'Soft-tissue ossification around the shoulders', 'XPO:0102484', 'abnormal interdigital region morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(21266, 'HP:0003837', 'Soft-tissue ossification around the shoulders', 'XPO:0103202', 'abnormal forelimb region morphology', 0.41935483870967744, 2.786899518863159, 1.0810641970914296, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(21267, 'HP:0003837', 'Soft-tissue ossification around the shoulders', 'XPO:0140179', 'abnormally necrotic postero-dorsal region', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(21268, 'HP:0003837', 'Soft-tissue ossification around the shoulders', 'XPO:0101702', 'abnormal anatomical system morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(21269, 'HP:0003837', 'Soft-tissue ossification around the shoulders', 'XPO:0101917', 'abnormal progenitor cell morphology', 0.4166666666666667, 2.786899518863159, 1.0775936770692605, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(21270, 'HP:0003837', 'Soft-tissue ossification around the shoulders', 'XPO:0141316', 'abnormal anatomical region morphology', 0.4482758620689655, 2.786899518863159, 1.1177207989108764, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(21271, 'HP:0003837', 'Soft-tissue ossification around the shoulders', 'XPO:0102092', 'abnormal ethmoid region morphology', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(21272, 'HP:0003837', 'Soft-tissue ossification around the shoulders', 'XPO:0102005', 'abnormal splanchnocranium morphology', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(21273, 'HP:0003837', 'Soft-tissue ossification around the shoulders', 'XPO:0102097', 'abnormal skeletal system morphology', 0.5714285714285714, 4.638757693672553, 1.628102786097549, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(21274, 'HP:0003837', 'Soft-tissue ossification around the shoulders', 'XPO:0129664', 'increased size of the skeleton', 0.45454545454545453, 4.638757693672553, 1.452076521536181, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(21275, 'HP:0003837', 'Soft-tissue ossification around the shoulders', 'XPO:0101927', 'abnormal extracellular matrix morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(21276, 'HP:0003837', 'Soft-tissue ossification around the shoulders', 'XPO:0129726', 'increased size of the axial skeleton', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(21277, 'HP:0003837', 'Soft-tissue ossification around the shoulders', 'XPO:0102336', 'abnormal Merkel cell morphology', 0.4166666666666667, 2.786899518863159, 1.0775936770692605, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(21278, 'HP:0003837', 'Soft-tissue ossification around the shoulders', 'XPO:0102542', 'abnormal vacuolated notochordal tissue morphology', 0.4878048780487805, 4.638757693672553, 1.5042634845863214, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(21279, 'HP:0003837', 'Soft-tissue ossification around the shoulders', 'XPO:0129582', 'increased size of the portion of organism substance', 0.41935483870967744, 2.786899518863159, 1.0810641970914296, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(21280, 'HP:0003837', 'Soft-tissue ossification around the shoulders', 'XPO:0101736', 'abnormal embryonic structure morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(21281, 'HP:0003837', 'Soft-tissue ossification around the shoulders', 'XPO:0102109', 'abnormal pericyte morphology', 0.4166666666666667, 2.786899518863159, 1.0775936770692605, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(21282, 'HP:0003837', 'Soft-tissue ossification around the shoulders', 'XPO:0102130', 'abnormal endoskeleton morphology', 0.5, 4.638757693672553, 1.5229507040072823, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(21283, 'HP:0003837', 'Soft-tissue ossification around the shoulders', 'XPO:0141703', 'abnormally necrotic posterior notochord', 0.47619047619047616, 4.638757693672553, 1.4862477031377266, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(21284, 'HP:0003837', 'Soft-tissue ossification around the shoulders', 'XPO:0140683', 'abnormally necrotic flexural organ', 0.47619047619047616, 4.638757693672553, 1.4862477031377266, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(21285, 'HP:0003837', 'Soft-tissue ossification around the shoulders', 'XPO:0140364', 'abnormally necrotic anterior region', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(21286, 'HP:0003837', 'Soft-tissue ossification around the shoulders', 'XPO:0102852', 'abnormal centriole morphology', 0.4166666666666667, 2.786899518863159, 1.0775936770692605, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(21287, 'HP:0003837', 'Soft-tissue ossification around the shoulders', 'XPO:0107349', 'abnormal left-right axis morphology', 0.41935483870967744, 2.786899518863159, 1.0810641970914296, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(21288, 'HP:0003837', 'Soft-tissue ossification around the shoulders', 'XPO:0102514', 'abnormal perichondrial cell morphology', 0.47619047619047616, 4.638757693672553, 1.4862477031377266, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(21289, 'HP:0006737', 'Extraadrenal pheochromocytoma', 'XPO:0101204', 'abnormal peripheral nerve', 0.45454545454545453, 7.318748312764234, 1.823925376359789, 'HP:0000759', 'Abnormal peripheral nervous system morphology'),
(21290, 'HP:0006737', 'Extraadrenal pheochromocytoma', 'XPO:0100114', 'abnormal peripheral nervous system', 0.40540540540540543, 6.642668884102504, 1.6410282971153933, 'HP:0410008', 'Abnormality of the peripheral nervous system'),
(21291, 'HP:0006737', 'Extraadrenal pheochromocytoma', 'XPO:0101030', 'abnormal spinal nerve', 0.43478260869565216, 7.318748312764234, 1.783834208610917, 'HP:0000759', 'Abnormal peripheral nervous system morphology'),
(21292, 'HP:0006737', 'Extraadrenal pheochromocytoma', 'XPO:0102366', 'abnormal lateral line system morphology', 0.425531914893617, 7.318748312764234, 1.7647552193307132, 'HP:0000759', 'Abnormal peripheral nervous system morphology'),
(21293, 'HP:0006737', 'Extraadrenal pheochromocytoma', 'XPO:0101746', 'abnormal peripheral nervous system morphology', 0.4444444444444444, 7.318748312764234, 1.8035456822313138, 'HP:0000759', 'Abnormal peripheral nervous system morphology'),
(21294, 'HP:0006737', 'Extraadrenal pheochromocytoma', 'XPO:0100167', 'abnormal nerve', 0.45454545454545453, 7.318748312764234, 1.823925376359789, 'HP:0000759', 'Abnormal peripheral nervous system morphology'),
(21295, 'HP:0006737', 'Extraadrenal pheochromocytoma', 'XPO:0100635', 'abnormal sympathetic chain', 0.4166666666666667, 7.318748312764234, 1.7462755978515432, 'HP:0000759', 'Abnormal peripheral nervous system morphology'),
(21296, 'HP:0006737', 'Extraadrenal pheochromocytoma', 'XPO:0101952', 'abnormal lateral line morphology', 0.40816326530612246, 7.318748312764234, 1.7283646054266224, 'HP:0000759', 'Abnormal peripheral nervous system morphology'),
(21297, 'HP:0002938', 'Lumbar hyperlordosis', 'XPO:0140510', 'abnormally necrotic postcranial axial skeleton', 0.4423076923076923, 6.272837960958401, 1.6656903922192745, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(21298, 'HP:0002938', 'Lumbar hyperlordosis', 'XPO:0102542', 'abnormal vacuolated notochordal tissue morphology', 0.43478260869565216, 4.638757693672553, 1.4201588541997616, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(21299, 'HP:0002938', 'Lumbar hyperlordosis', 'XPO:0102351', 'abnormal sphenoid region morphology', 0.40350877192982454, 6.272837960958401, 1.5909573036826314, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(21300, 'HP:0002938', 'Lumbar hyperlordosis', 'XPO:0130368', 'increased size of the elastica externa', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(21301, 'HP:0002938', 'Lumbar hyperlordosis', 'XPO:0128580', 'decreased size of the postcranial axial skeleton', 0.42592592592592593, 6.272837960958401, 1.6345532468244968, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(21302, 'HP:0002938', 'Lumbar hyperlordosis', 'XPO:0100693', 'abnormal vertebral centrum', 0.5102040816326531, 8.05344015541032, 2.0270416962841815, 'UPHENO:0002813', 'abnormal vertebral column'),
(21303, 'HP:0002938', 'Lumbar hyperlordosis', 'XPO:0100895', 'abnormal presacral vertebra', 0.4166666666666667, 8.05344015541032, 1.8318297040812228, 'UPHENO:0002813', 'abnormal vertebral column'),
(21304, 'HP:0002938', 'Lumbar hyperlordosis', 'XPO:0141708', 'decreased size of the posterior notochord', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(21305, 'HP:0002938', 'Lumbar hyperlordosis', 'XPO:0141723', 'abnormal posterior notochord morphology', 0.47619047619047616, 4.638757693672553, 1.4862477031377266, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(21306, 'HP:0002938', 'Lumbar hyperlordosis', 'XPO:0101860', 'abnormal skeletal subdivision morphology', 0.46511627906976744, 4.638757693672553, 1.4688640910537754, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(21307, 'HP:0002938', 'Lumbar hyperlordosis', 'XPO:0141703', 'abnormally necrotic posterior notochord', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(21308, 'HP:0002938', 'Lumbar hyperlordosis', 'XPO:0102130', 'abnormal endoskeleton morphology', 0.4444444444444444, 4.638757693672553, 1.4358516936218344, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(21309, 'HP:0002938', 'Lumbar hyperlordosis', 'XPO:0101070', 'abnormal rib', 0.4098360655737705, 8.05344015541032, 1.816752660002781, 'UPHENO:0002813', 'abnormal vertebral column'),
(21310, 'HP:0002938', 'Lumbar hyperlordosis', 'XPO:0128227', 'decreased size of the vertebral column', 0.4727272727272727, 8.361863005979023, 1.9881852765111048, 'UPHENO:0076695', 'abnormal vertebral column morphology'),
(21311, 'HP:0002938', 'Lumbar hyperlordosis', 'XPO:0102164', 'abnormal mandibular mesenchyme morphology', 0.4117647058823529, 6.211345574613551, 1.599253852164941, 'UPHENO:0087089', 'abnormal axial skeleton plus cranial skeleton morphology'),
(21312, 'HP:0002938', 'Lumbar hyperlordosis', 'XPO:0140019', 'abnormally necrotic skeletal system', 0.4444444444444444, 4.638757693672553, 1.4358516936218344, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(21313, 'HP:0002938', 'Lumbar hyperlordosis', 'XPO:0141713', 'increased size of the posterior notochord', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(21314, 'HP:0002938', 'Lumbar hyperlordosis', 'XPO:0140432', 'abnormally necrotic skeleton', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(21315, 'HP:0002938', 'Lumbar hyperlordosis', 'XPO:0128890', 'decreased size of the elastica externa', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(21316, 'HP:0002938', 'Lumbar hyperlordosis', 'XPO:0128352', 'decreased size of the skeletal system', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(21317, 'HP:0002938', 'Lumbar hyperlordosis', 'XPO:0140852', 'abnormally necrotic vertebral centrum', 0.40625, 8.361863005979023, 1.843097079965941, 'UPHENO:0076695', 'abnormal vertebral column morphology'),
(21318, 'HP:0002938', 'Lumbar hyperlordosis', 'XPO:0101976', 'abnormal portion of organism substance morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(21319, 'HP:0002938', 'Lumbar hyperlordosis', 'XPO:0126787', 'abnormally localised vertebral centrum', 0.4166666666666667, 8.05344015541032, 1.8318297040812228, 'UPHENO:0002813', 'abnormal vertebral column'),
(21320, 'HP:0002938', 'Lumbar hyperlordosis', 'XPO:0130908', 'increased size of the notochordal sheath', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(21321, 'HP:0002938', 'Lumbar hyperlordosis', 'XPO:0101957', 'abnormal axial skeleton morphology', 0.4666666666666667, 6.211345574613551, 1.702535736723214, 'UPHENO:0087089', 'abnormal axial skeleton plus cranial skeleton morphology'),
(21322, 'HP:0002938', 'Lumbar hyperlordosis', 'XPO:0129664', 'increased size of the skeleton', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(21323, 'HP:0002938', 'Lumbar hyperlordosis', 'XPO:0102605', 'abnormal dermal skeleton morphology', 0.4444444444444444, 4.638757693672553, 1.4358516936218344, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(21324, 'HP:0002938', 'Lumbar hyperlordosis', 'XPO:0102217', 'abnormal elastica externa morphology', 0.5, 4.638757693672553, 1.5229507040072823, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(21325, 'HP:0002938', 'Lumbar hyperlordosis', 'XPO:0101982', 'abnormal appendicular skeleton morphology', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(21326, 'HP:0002938', 'Lumbar hyperlordosis', 'XPO:0101226', 'abnormal postsacral vertebra', 0.4166666666666667, 8.05344015541032, 1.8318297040812228, 'UPHENO:0002813', 'abnormal vertebral column'),
(21327, 'HP:0002938', 'Lumbar hyperlordosis', 'XPO:0141709', 'increased size of the anterior notochord', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(21328, 'HP:0002938', 'Lumbar hyperlordosis', 'XPO:0140043', 'abnormally necrotic perichondrium', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(21329, 'HP:0002938', 'Lumbar hyperlordosis', 'XPO:0128709', 'decreased size of the flexural organ', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(21330, 'HP:0002938', 'Lumbar hyperlordosis', 'XPO:0139795', 'abnormally necrotic vertebral element', 0.4126984126984127, 8.361863005979023, 1.8576672440911264, 'UPHENO:0076695', 'abnormal vertebral column morphology'),
(21331, 'HP:0002938', 'Lumbar hyperlordosis', 'XPO:0130060', 'increased size of the postcranial axial skeleton', 0.42592592592592593, 6.272837960958401, 1.6345532468244968, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(21332, 'HP:0002938', 'Lumbar hyperlordosis', 'XPO:0101446', 'abnormal transverse process', 0.4098360655737705, 8.05344015541032, 1.816752660002781, 'UPHENO:0002813', 'abnormal vertebral column'),
(21333, 'HP:0002938', 'Lumbar hyperlordosis', 'XPO:0127548', 'abnormally localised vertebral element', 0.423728813559322, 8.05344015541032, 1.8472884566637167, 'UPHENO:0002813', 'abnormal vertebral column'),
(21334, 'HP:0002938', 'Lumbar hyperlordosis', 'XPO:0102564', 'abnormal olfactory region morphology', 0.40350877192982454, 6.272837960958401, 1.5909573036826314, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(21335, 'HP:0002938', 'Lumbar hyperlordosis', 'XPO:0129786', 'increased size of the articular system', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(21336, 'HP:0002938', 'Lumbar hyperlordosis', 'XPO:0103116', 'abnormal bone marrow morphology', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(21337, 'HP:0002938', 'Lumbar hyperlordosis', 'XPO:0100226', 'abnormal vertebral element', 0.5208333333333334, 8.05344015541032, 2.048047870764469, 'UPHENO:0002813', 'abnormal vertebral column'),
(21338, 'HP:0002938', 'Lumbar hyperlordosis', 'XPO:0102401', 'abnormal neurocranium morphology', 0.40350877192982454, 6.272837960958401, 1.5909573036826314, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(21339, 'HP:0002938', 'Lumbar hyperlordosis', 'XPO:0102806', 'abnormal articular system morphology', 0.4878048780487805, 4.638757693672553, 1.5042634845863214, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(21340, 'HP:0002938', 'Lumbar hyperlordosis', 'XPO:0140683', 'abnormally necrotic flexural organ', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(21341, 'HP:0002938', 'Lumbar hyperlordosis', 'XPO:0141719', 'abnormal anterior notochord morphology', 0.47619047619047616, 4.638757693672553, 1.4862477031377266, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(21342, 'HP:0002938', 'Lumbar hyperlordosis', 'XPO:0139771', 'abnormally necrotic skeletal subdivision', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(21343, 'HP:0002938', 'Lumbar hyperlordosis', 'XPO:0140103', 'abnormally necrotic vertebral column', 0.49056603773584906, 8.361863005979023, 2.025350834530429, 'UPHENO:0076695', 'abnormal vertebral column morphology'),
(21344, 'HP:0002938', 'Lumbar hyperlordosis', 'XPO:0102010', 'abnormal perichondrium morphology', 0.46511627906976744, 4.638757693672553, 1.4688640910537754, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(21345, 'HP:0002938', 'Lumbar hyperlordosis', 'XPO:0140559', 'abnormally necrotic articular system', 0.43478260869565216, 4.638757693672553, 1.4201588541997616, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(21346, 'HP:0002938', 'Lumbar hyperlordosis', 'XPO:0102728', 'abnormal tendon morphology', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(21347, 'HP:0002938', 'Lumbar hyperlordosis', 'XPO:0141699', 'abnormally necrotic anterior notochord', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(21348, 'HP:0002938', 'Lumbar hyperlordosis', 'XPO:0102113', 'abnormal anatomical line morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(21349, 'HP:0002938', 'Lumbar hyperlordosis', 'XPO:0129434', 'decreased size of the notochordal sheath', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(21350, 'HP:0002938', 'Lumbar hyperlordosis', 'XPO:0102216', 'abnormal vertebral column morphology', 0.5531914893617021, 8.361863005979023, 2.15074671919221, 'UPHENO:0076695', 'abnormal vertebral column morphology'),
(21351, 'HP:0002938', 'Lumbar hyperlordosis', 'XPO:0102461', 'abnormal postcranial axial skeleton morphology', 0.5, 6.272837960958401, 1.770993783297728, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(21352, 'HP:0002938', 'Lumbar hyperlordosis', 'XPO:0102980', 'abnormal perichordal tissue morphology', 0.43478260869565216, 4.638757693672553, 1.4201588541997616, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(21353, 'HP:0002938', 'Lumbar hyperlordosis', 'XPO:0139774', 'abnormally necrotic elastica externa', 0.4444444444444444, 4.638757693672553, 1.4358516936218344, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(21354, 'HP:0002938', 'Lumbar hyperlordosis', 'XPO:0102144', 'abnormal cranial skeleton morphology', 0.45652173913043476, 6.211345574613551, 1.6839282300806968, 'UPHENO:0087089', 'abnormal axial skeleton plus cranial skeleton morphology'),
(21355, 'HP:0002938', 'Lumbar hyperlordosis', 'XPO:0102093', 'abnormal craniofacial skeleton morphology', 0.4375, 6.211345574613551, 1.6484731386629958, 'UPHENO:0087089', 'abnormal axial skeleton plus cranial skeleton morphology'),
(21356, 'HP:0002938', 'Lumbar hyperlordosis', 'XPO:0125260', 'absent vertebral column', 0.46296296296296297, 8.05344015541032, 1.9309180501496346, 'UPHENO:0002813', 'abnormal vertebral column'),
(21357, 'HP:0002938', 'Lumbar hyperlordosis', 'XPO:0141704', 'decreased size of the anterior notochord', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(21358, 'HP:0002938', 'Lumbar hyperlordosis', 'XPO:0103218', 'abnormal joint morphology', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(21359, 'HP:0002938', 'Lumbar hyperlordosis', 'XPO:0101858', 'abnormal vertebral element morphology', 0.4727272727272727, 8.361863005979023, 1.9881852765111048, 'UPHENO:0076695', 'abnormal vertebral column morphology'),
(21360, 'HP:0002938', 'Lumbar hyperlordosis', 'XPO:0102272', 'abnormal notochordal sheath morphology', 0.47619047619047616, 4.638757693672553, 1.4862477031377266, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(21361, 'HP:0002938', 'Lumbar hyperlordosis', 'XPO:0101680', 'abnormal skeletal element morphology', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(21362, 'HP:0002938', 'Lumbar hyperlordosis', 'XPO:0129707', 'increased size of the vertebral column', 0.4727272727272727, 8.361863005979023, 1.9881852765111048, 'UPHENO:0076695', 'abnormal vertebral column morphology'),
(21363, 'HP:0002938', 'Lumbar hyperlordosis', 'XPO:0129832', 'increased size of the skeletal system', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(21364, 'HP:0002938', 'Lumbar hyperlordosis', 'XPO:0126886', 'abnormally localised vertebral column', 0.49019607843137253, 8.05344015541032, 1.9868982817607654, 'UPHENO:0002813', 'abnormal vertebral column'),
(21365, 'HP:0002938', 'Lumbar hyperlordosis', 'XPO:0102514', 'abnormal perichondrial cell morphology', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(21366, 'HP:0002938', 'Lumbar hyperlordosis', 'XPO:0130188', 'increased size of the flexural organ', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(21367, 'HP:0002938', 'Lumbar hyperlordosis', 'XPO:0100253', 'abnormal vertebra', 0.423728813559322, 8.05344015541032, 1.8472884566637167, 'UPHENO:0002813', 'abnormal vertebral column'),
(21368, 'HP:0002938', 'Lumbar hyperlordosis', 'XPO:0139998', 'abnormally necrotic axial skeleton', 0.4117647058823529, 6.211345574613551, 1.599253852164941, 'UPHENO:0087089', 'abnormal axial skeleton plus cranial skeleton morphology'),
(21369, 'HP:0002938', 'Lumbar hyperlordosis', 'XPO:0100252', 'abnormal caudal vertebra', 0.4032258064516129, 8.05344015541032, 1.8020418700394085, 'UPHENO:0002813', 'abnormal vertebral column'),
(21370, 'HP:0002938', 'Lumbar hyperlordosis', 'XPO:0100927', 'abnormal sacral vertebra', 0.4166666666666667, 8.05344015541032, 1.8318297040812228, 'UPHENO:0002813', 'abnormal vertebral column'),
(21371, 'HP:0002938', 'Lumbar hyperlordosis', 'XPO:0102567', 'abnormal skeleton morphology', 0.47619047619047616, 4.638757693672553, 1.4862477031377266, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(21372, 'HP:0002938', 'Lumbar hyperlordosis', 'XPO:0103152', 'abnormal otic region morphology', 0.40350877192982454, 6.272837960958401, 1.5909573036826314, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(21373, 'HP:0002938', 'Lumbar hyperlordosis', 'XPO:0140350', 'abnormally necrotic notochordal sheath', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(21374, 'HP:0002938', 'Lumbar hyperlordosis', 'XPO:0102828', 'abnormal occipital region morphology', 0.4107142857142857, 6.272837960958401, 1.6050994245019483, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(21375, 'HP:0002938', 'Lumbar hyperlordosis', 'XPO:0139889', 'abnormally necrotic cranial skeleton', 0.40384615384615385, 6.211345574613551, 1.5838017617482976, 'UPHENO:0087089', 'abnormal axial skeleton plus cranial skeleton morphology'),
(21376, 'HP:0002938', 'Lumbar hyperlordosis', 'XPO:0100584', 'abnormal vertebral column', 0.5952380952380952, 8.05344015541032, 2.1894552697464333, 'UPHENO:0002813', 'abnormal vertebral column'),
(21377, 'HP:0002938', 'Lumbar hyperlordosis', 'XPO:0128306', 'decreased size of the articular system', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(21378, 'HP:0002938', 'Lumbar hyperlordosis', 'XPO:0128184', 'decreased size of the skeleton', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(21379, 'HP:0002938', 'Lumbar hyperlordosis', 'XPO:0102054', 'abnormal notochord morphology', 0.47619047619047616, 4.638757693672553, 1.4862477031377266, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(21380, 'HP:0002938', 'Lumbar hyperlordosis', 'XPO:0102097', 'abnormal skeletal system morphology', 0.5, 4.638757693672553, 1.5229507040072823, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(21381, 'HP:0002938', 'Lumbar hyperlordosis', 'XPO:0139917', 'abnormally necrotic notochord', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(21382, 'HP:0002938', 'Lumbar hyperlordosis', 'XPO:0107372', 'abnormal flexural organ morphology', 0.47619047619047616, 4.638757693672553, 1.4862477031377266, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(21383, 'HP:0002938', 'Lumbar hyperlordosis', 'XPO:0101713', 'abnormal anatomical entity in vitro morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(21384, 'HP:0002938', 'Lumbar hyperlordosis', 'XPO:0102325', 'abnormal vertebral centrum morphology', 0.4642857142857143, 8.361863005979023, 1.9703536582274415, 'UPHENO:0076695', 'abnormal vertebral column morphology'),
(21385, 'HP:0002938', 'Lumbar hyperlordosis', 'XPO:0101638', 'abnormal anatomical structure morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(21386, 'HP:0010634', 'Total hyposmia', 'XPO:0127208', 'abnormally localised olfactory pit', 0.4489795918367347, 9.116652820832241, 2.023163627197384, 'HP:0000366', 'Abnormality of the nose'),
(21387, 'HP:0010634', 'Total hyposmia', 'XPO:0127893', 'abnormally localised Jacobsons organ', 0.4230769230769231, 9.116652820832241, 1.9639362067537367, 'HP:0000366', 'Abnormality of the nose'),
(21388, 'HP:0010634', 'Total hyposmia', 'XPO:0100594', 'abnormal Jacobsons organ', 0.4772727272727273, 9.116652820832241, 2.0859361820049065, 'HP:0000366', 'Abnormality of the nose'),
(21389, 'HP:0010634', 'Total hyposmia', 'XPO:0101334', 'abnormal olfactory pit', 0.4883720930232558, 9.116652820832241, 2.110051852319324, 'HP:0000366', 'Abnormality of the nose'),
(21390, 'HP:0010634', 'Total hyposmia', 'XPO:0103304', 'absent olfactory pit', 0.4074074074074074, 9.116652820832241, 1.927223881641334, 'HP:0000366', 'Abnormality of the nose'),
(21391, 'HP:0410254', 'Cyclic neutropenia in myeloid maturation arrest in bone marrow', 'XPO:0131221', 'abnormally decreased number of thymocyte', 0.40186915887850466, 9.649807419403725, 1.9692536634408806, 'UPHENO:0085330', 'abnormally decreased number of leukocyte'),
(21392, 'HP:0100401', 'Duplication of the middle phalanx of the 3rd toe', 'XPO:0100178', 'abnormal digit', 0.4117647058823529, 6.393467666143939, 1.622530225640833, 'HP:0011297', 'Abnormal digit morphology'),
(21393, 'HP:0100401', 'Duplication of the middle phalanx of the 3rd toe', 'XPO:0102566', 'abnormal claw primordium morphology', 0.40217391304347827, 7.639349617137506, 1.7528112073555977, 'HP:0001780', 'Abnormal toe morphology'),
(21394, 'HP:0012648', 'Decreased inflammatory response', 'XPO:0100581', 'abnormal immune system', 0.43333333333333335, 5.64885357140806, 1.5645563421015427, 'HP:0002715', 'Abnormality of the immune system'),
(21395, 'HP:0012648', 'Decreased inflammatory response', 'XPO:0101451', 'abnormal dorsal lymph space', 0.40625, 5.64885357140806, 1.5148751642906173, 'HP:0002715', 'Abnormality of the immune system'),
(21396, 'HP:0012648', 'Decreased inflammatory response', 'XPO:0100232', 'abnormal lymphatic system', 0.43333333333333335, 5.64885357140806, 1.5645563421015427, 'HP:0002715', 'Abnormality of the immune system'),
(21397, 'HP:0012648', 'Decreased inflammatory response', 'XPO:0100599', 'abnormal adult immune system', 0.41935483870967744, 5.64885357140806, 1.5391147060347428, 'HP:0002715', 'Abnormality of the immune system'),
(21398, 'HP:0012648', 'Decreased inflammatory response', 'XPO:0101221', 'abnormal larval immune system', 0.41935483870967744, 5.64885357140806, 1.5391147060347428, 'HP:0002715', 'Abnormality of the immune system'),
(21399, 'HP:0100510', 'Low levels of vitamin C', 'XPO:0141882', 'abnormal gamma-aminobutyric acid metabolic process', 0.6379310344827587, 9.417633977274692, 2.4510815950316345, 'HP:0032245', 'Abnormal metabolism'),
(21400, 'HP:0100510', 'Low levels of vitamin C', 'XPO:0141853', 'abnormal glutamate metabolic process', 0.5967741935483871, 9.417633977274692, 2.3706962947459114, 'HP:0032245', 'Abnormal metabolism'),
(21401, 'HP:0100510', 'Low levels of vitamin C', 'XPO:0141918', 'abnormal tyrosine metabolic process', 0.6166666666666667, 9.417633977274692, 2.40988401228207, 'HP:0032245', 'Abnormal metabolism'),
(21402, 'HP:0100510', 'Low levels of vitamin C', 'XPO:0141888', 'abnormal threonine metabolic process', 0.6166666666666667, 9.417633977274692, 2.40988401228207, 'HP:0032245', 'Abnormal metabolism'),
(21403, 'HP:0100510', 'Low levels of vitamin C', 'XPO:0141887', 'abnormal histidine metabolic process', 0.6166666666666667, 9.417633977274692, 2.40988401228207, 'HP:0032245', 'Abnormal metabolism'),
(21404, 'HP:0100510', 'Low levels of vitamin C', 'XPO:0141917', 'abnormal tryptophan metabolic process', 0.6166666666666667, 9.417633977274692, 2.40988401228207, 'HP:0032245', 'Abnormal metabolism'),
(21405, 'HP:0100510', 'Low levels of vitamin C', 'XPO:0141889', 'abnormal homoserine metabolic process', 0.6065573770491803, 9.417633977274692, 2.390049238669567, 'HP:0032245', 'Abnormal metabolism'),
(21406, 'HP:0100510', 'Low levels of vitamin C', 'XPO:0141896', 'abnormal lysine metabolic process', 0.6166666666666667, 9.417633977274692, 2.40988401228207, 'HP:0032245', 'Abnormal metabolism'),
(21407, 'HP:0100510', 'Low levels of vitamin C', 'XPO:0141912', 'abnormal D-serine metabolic process', 0.6065573770491803, 9.417633977274692, 2.390049238669567, 'HP:0032245', 'Abnormal metabolism'),
(21408, 'HP:0100510', 'Low levels of vitamin C', 'XPO:0141847', 'abnormal arginine metabolic process', 0.6166666666666667, 9.417633977274692, 2.40988401228207, 'HP:0032245', 'Abnormal metabolism'),
(21409, 'HP:0100510', 'Low levels of vitamin C', 'XPO:0141843', 'abnormal alanine metabolic process', 0.6271186440677966, 9.417633977274692, 2.430220946777333, 'HP:0032245', 'Abnormal metabolism'),
(21410, 'HP:0100510', 'Low levels of vitamin C', 'XPO:0141868', 'abnormal asparagine metabolic process', 0.6166666666666667, 9.417633977274692, 2.40988401228207, 'HP:0032245', 'Abnormal metabolism'),
(21411, 'HP:0100510', 'Low levels of vitamin C', 'XPO:0141905', 'abnormal ornithine metabolic process', 0.6271186440677966, 9.417633977274692, 2.430220946777333, 'HP:0032245', 'Abnormal metabolism'),
(21412, 'HP:0100510', 'Low levels of vitamin C', 'XPO:0141848', 'abnormal proline metabolic process', 0.6166666666666667, 9.417633977274692, 2.40988401228207, 'HP:0032245', 'Abnormal metabolism'),
(21413, 'HP:0100510', 'Low levels of vitamin C', 'XPO:0141922', 'abnormal valine metabolic process', 0.6166666666666667, 9.417633977274692, 2.40988401228207, 'HP:0032245', 'Abnormal metabolism'),
(21414, 'HP:0100510', 'Low levels of vitamin C', 'XPO:0141913', 'abnormal L-serine metabolic process', 0.6065573770491803, 9.417633977274692, 2.390049238669567, 'HP:0032245', 'Abnormal metabolism'),
(21415, 'HP:0100510', 'Low levels of vitamin C', 'XPO:0141857', 'abnormal glycine metabolic process', 0.6065573770491803, 9.417633977274692, 2.390049238669567, 'HP:0032245', 'Abnormal metabolism'),
(21416, 'HP:0100510', 'Low levels of vitamin C', 'XPO:0141869', 'abnormal alpha-amino acid metabolic process', 0.6491228070175439, 9.417633977274692, 2.472488827637517, 'HP:0032245', 'Abnormal metabolism'),
(21417, 'HP:0100510', 'Low levels of vitamin C', 'XPO:0141858', 'abnormal serine family amino acid metabolic process', 0.6271186440677966, 9.417633977274692, 2.430220946777333, 'HP:0032245', 'Abnormal metabolism'),
(21418, 'HP:0100510', 'Low levels of vitamin C', 'XPO:0141873', 'abnormal tricarboxylic acid metabolic process', 0.6363636363636364, 9.119292702704945, 2.4089803372708736, 'HP:0004354', 'Abnormal circulating carboxylic acid concentration'),
(21419, 'HP:0100510', 'Low levels of vitamin C', 'XPO:0141893', 'abnormal isoleucine metabolic process', 0.6166666666666667, 9.417633977274692, 2.40988401228207, 'HP:0032245', 'Abnormal metabolism'),
(21420, 'HP:0100510', 'Low levels of vitamin C', 'XPO:0141895', 'abnormal leucine metabolic process', 0.6166666666666667, 9.417633977274692, 2.40988401228207, 'HP:0032245', 'Abnormal metabolism'),
(21421, 'HP:0025109', 'Reduced red cell pyruvate kinase level', 'XPO:0102386', 'abnormal electrically active cell morphology', 0.43902439024390244, 5.43643956286526, 1.5449043867452603, 'HP:0025461', 'Abnormal cell morphology'),
(21422, 'HP:0025109', 'Reduced red cell pyruvate kinase level', 'XPO:0103005', 'abnormal oxygen accumulating cell morphology', 0.43902439024390244, 5.43643956286526, 1.5449043867452603, 'HP:0025461', 'Abnormal cell morphology'),
(21423, 'HP:0025109', 'Reduced red cell pyruvate kinase level', 'XPO:0101804', 'abnormal stem cell morphology', 0.43902439024390244, 5.43643956286526, 1.5449043867452603, 'HP:0025461', 'Abnormal cell morphology'),
(21424, 'HP:0025109', 'Reduced red cell pyruvate kinase level', 'XPO:0102764', 'abnormal apoptotic cell morphology', 0.43902439024390244, 5.43643956286526, 1.5449043867452603, 'HP:0025461', 'Abnormal cell morphology'),
(21425, 'HP:0025109', 'Reduced red cell pyruvate kinase level', 'XPO:0102347', 'abnormal ciliated cell morphology', 0.43902439024390244, 5.43643956286526, 1.5449043867452603, 'HP:0025461', 'Abnormal cell morphology'),
(21426, 'HP:0025109', 'Reduced red cell pyruvate kinase level', 'XPO:0102306', 'abnormal secondary oogonium morphology', 0.4186046511627907, 5.43643956286526, 1.5085486027240909, 'HP:0025461', 'Abnormal cell morphology'),
(21427, 'HP:0025109', 'Reduced red cell pyruvate kinase level', 'XPO:0102608', 'abnormal multiciliated cell morphology', 0.4186046511627907, 5.43643956286526, 1.5085486027240909, 'HP:0025461', 'Abnormal cell morphology'),
(21428, 'HP:0025109', 'Reduced red cell pyruvate kinase level', 'XPO:0139717', 'abnormally necrotic cell', 0.42857142857142855, 5.43643956286526, 1.526401870347189, 'HP:0025461', 'Abnormal cell morphology'),
(21429, 'HP:0025109', 'Reduced red cell pyruvate kinase level', 'XPO:0102069', 'abnormal proepicardium morphology', 0.4186046511627907, 5.43643956286526, 1.5085486027240909, 'HP:0025461', 'Abnormal cell morphology'),
(21430, 'HP:0025109', 'Reduced red cell pyruvate kinase level', 'XPO:0102336', 'abnormal Merkel cell morphology', 0.43902439024390244, 5.43643956286526, 1.5449043867452603, 'HP:0025461', 'Abnormal cell morphology'),
(21431, 'HP:0025109', 'Reduced red cell pyruvate kinase level', 'XPO:0103167', 'abnormal absorptive cell morphology', 0.43902439024390244, 5.43643956286526, 1.5449043867452603, 'HP:0025461', 'Abnormal cell morphology'),
(21432, 'HP:0025109', 'Reduced red cell pyruvate kinase level', 'XPO:0101657', 'abnormal oocyte morphology', 0.4186046511627907, 5.43643956286526, 1.5085486027240909, 'HP:0025461', 'Abnormal cell morphology'),
(21433, 'HP:0025109', 'Reduced red cell pyruvate kinase level', 'XPO:0101921', 'abnormal chondroblast morphology', 0.43902439024390244, 5.43643956286526, 1.5449043867452603, 'HP:0025461', 'Abnormal cell morphology'),
(21434, 'HP:0025109', 'Reduced red cell pyruvate kinase level', 'XPO:0102636', 'abnormal acid secreting cell morphology', 0.43902439024390244, 5.43643956286526, 1.5449043867452603, 'HP:0025461', 'Abnormal cell morphology'),
(21435, 'HP:0025109', 'Reduced red cell pyruvate kinase level', 'XPO:0102958', 'abnormal cementoblast morphology', 0.43902439024390244, 5.43643956286526, 1.5449043867452603, 'HP:0025461', 'Abnormal cell morphology'),
(21436, 'HP:0025109', 'Reduced red cell pyruvate kinase level', 'XPO:0102534', 'abnormal spermatocyte morphology', 0.4186046511627907, 5.43643956286526, 1.5085486027240909, 'HP:0025461', 'Abnormal cell morphology'),
(21437, 'HP:0025109', 'Reduced red cell pyruvate kinase level', 'XPO:0103219', 'abnormal hemangioblast morphology', 0.4444444444444444, 5.574066539846944, 1.573964074113079, 'HP:0001871', 'Abnormality of blood and blood-forming tissues'),
(21438, 'HP:0025109', 'Reduced red cell pyruvate kinase level', 'XPO:0102165', 'abnormal melanoblast morphology', 0.43902439024390244, 5.43643956286526, 1.5449043867452603, 'HP:0025461', 'Abnormal cell morphology'),
(21439, 'HP:0025109', 'Reduced red cell pyruvate kinase level', 'XPO:0102323', 'abnormal keratin accumulating cell morphology', 0.43902439024390244, 5.43643956286526, 1.5449043867452603, 'HP:0025461', 'Abnormal cell morphology'),
(21440, 'HP:0025109', 'Reduced red cell pyruvate kinase level', 'XPO:0102434', 'abnormal exocrine cell morphology', 0.43902439024390244, 5.43643956286526, 1.5449043867452603, 'HP:0025461', 'Abnormal cell morphology'),
(21441, 'HP:0025109', 'Reduced red cell pyruvate kinase level', 'XPO:0102061', 'abnormal spermatid morphology', 0.4186046511627907, 5.43643956286526, 1.5085486027240909, 'HP:0025461', 'Abnormal cell morphology'),
(21442, 'HP:0025109', 'Reduced red cell pyruvate kinase level', 'XPO:0102181', 'abnormal mitotic cell morphology', 0.43902439024390244, 5.43643956286526, 1.5449043867452603, 'HP:0025461', 'Abnormal cell morphology'),
(21443, 'HP:0025109', 'Reduced red cell pyruvate kinase level', 'XPO:0103099', 'abnormal alkali secreting cell morphology', 0.43902439024390244, 5.43643956286526, 1.5449043867452603, 'HP:0025461', 'Abnormal cell morphology'),
(21444, 'HP:0025109', 'Reduced red cell pyruvate kinase level', 'XPO:0101850', 'abnormal epithelial cell morphology', 0.4090909090909091, 5.43643956286526, 1.491307481034791, 'HP:0025461', 'Abnormal cell morphology'),
(21445, 'HP:0025109', 'Reduced red cell pyruvate kinase level', 'XPO:0102965', 'abnormal barrier epithelial cell morphology', 0.43902439024390244, 5.43643956286526, 1.5449043867452603, 'HP:0025461', 'Abnormal cell morphology'),
(21446, 'HP:0025109', 'Reduced red cell pyruvate kinase level', 'XPO:0101940', 'abnormal early embryonic cell morphology', 0.4186046511627907, 5.43643956286526, 1.5085486027240909, 'HP:0025461', 'Abnormal cell morphology'),
(21447, 'HP:0025109', 'Reduced red cell pyruvate kinase level', 'XPO:0102869', 'abnormal mucus secreting cell morphology', 0.43902439024390244, 5.43643956286526, 1.5449043867452603, 'HP:0025461', 'Abnormal cell morphology'),
(21448, 'HP:0025109', 'Reduced red cell pyruvate kinase level', 'XPO:0102109', 'abnormal pericyte morphology', 0.43902439024390244, 5.43643956286526, 1.5449043867452603, 'HP:0025461', 'Abnormal cell morphology'),
(21449, 'HP:0025109', 'Reduced red cell pyruvate kinase level', 'XPO:0102872', 'abnormal ciliated non-epidermal cell morphology', 0.4186046511627907, 5.43643956286526, 1.5085486027240909, 'HP:0025461', 'Abnormal cell morphology'),
(21450, 'HP:0025109', 'Reduced red cell pyruvate kinase level', 'XPO:0102531', 'abnormal secondary spermatogonium morphology', 0.4186046511627907, 5.43643956286526, 1.5085486027240909, 'HP:0025461', 'Abnormal cell morphology'),
(21451, 'HP:0025109', 'Reduced red cell pyruvate kinase level', 'XPO:0102423', 'abnormal multiciliated cell precursor morphology', 0.43902439024390244, 5.43643956286526, 1.5449043867452603, 'HP:0025461', 'Abnormal cell morphology'),
(21452, 'HP:0025109', 'Reduced red cell pyruvate kinase level', 'XPO:0140973', 'abnormally necrotic erythroid cell', 0.40816326530612246, 5.574066539846944, 1.5083531416540121, 'HP:0001871', 'Abnormality of blood and blood-forming tissues'),
(21453, 'HP:0025109', 'Reduced red cell pyruvate kinase level', 'XPO:0101917', 'abnormal progenitor cell morphology', 0.43902439024390244, 5.43643956286526, 1.5449043867452603, 'HP:0025461', 'Abnormal cell morphology'),
(21454, 'HP:0025109', 'Reduced red cell pyruvate kinase level', 'XPO:0140429', 'abnormally necrotic hemangioblast', 0.40816326530612246, 5.574066539846944, 1.5083531416540121, 'UPHENO:0004459', 'abnormal hematopoietic system'),
(21455, 'HP:0025109', 'Reduced red cell pyruvate kinase level', 'XPO:0103067', 'abnormal paracrine cell morphology', 0.43902439024390244, 5.43643956286526, 1.5449043867452603, 'HP:0025461', 'Abnormal cell morphology'),
(21456, 'HP:0025109', 'Reduced red cell pyruvate kinase level', 'XPO:0107371', 'abnormal migrating myoblast morphology', 0.4186046511627907, 5.43643956286526, 1.5085486027240909, 'HP:0025461', 'Abnormal cell morphology'),
(21457, 'HP:0025109', 'Reduced red cell pyruvate kinase level', 'XPO:0102147', 'abnormal somatic stem cell morphology', 0.4186046511627907, 5.43643956286526, 1.5085486027240909, 'HP:0025461', 'Abnormal cell morphology'),
(21458, 'HP:0025109', 'Reduced red cell pyruvate kinase level', 'XPO:0102860', 'abnormal mesenchymal stem cell morphology', 0.4186046511627907, 5.43643956286526, 1.5085486027240909, 'HP:0025461', 'Abnormal cell morphology'),
(21459, 'HP:0025109', 'Reduced red cell pyruvate kinase level', 'XPO:0103082', 'abnormal myeloid cell morphology', 0.4444444444444444, 5.574066539846944, 1.573964074113079, 'UPHENO:0004459', 'abnormal hematopoietic system'),
(21460, 'HP:0025109', 'Reduced red cell pyruvate kinase level', 'XPO:0103080', 'abnormal myelin accumulating cell morphology', 0.43902439024390244, 5.43643956286526, 1.5449043867452603, 'HP:0025461', 'Abnormal cell morphology'),
(21461, 'HP:0025109', 'Reduced red cell pyruvate kinase level', 'XPO:0102873', 'abnormal nucleate erythrocyte morphology', 0.43902439024390244, 5.43643956286526, 1.5449043867452603, 'HP:0025461', 'Abnormal cell morphology'),
(21462, 'HP:0025109', 'Reduced red cell pyruvate kinase level', 'XPO:0102258', 'abnormal primordial germ cell morphology', 0.4186046511627907, 5.43643956286526, 1.5085486027240909, 'HP:0025461', 'Abnormal cell morphology'),
(21463, 'HP:0025109', 'Reduced red cell pyruvate kinase level', 'XPO:0102285', 'abnormal myoblast morphology', 0.43902439024390244, 5.43643956286526, 1.5449043867452603, 'HP:0025461', 'Abnormal cell morphology'),
(21464, 'HP:0025109', 'Reduced red cell pyruvate kinase level', 'XPO:0101969', 'abnormal zygote morphology', 0.43902439024390244, 5.43643956286526, 1.5449043867452603, 'HP:0025461', 'Abnormal cell morphology'),
(21465, 'HP:0025109', 'Reduced red cell pyruvate kinase level', 'XPO:0101636', 'abnormal cell morphology', 0.46153846153846156, 5.43643956286526, 1.5840220806831131, 'HP:0025461', 'Abnormal cell morphology'),
(21466, 'HP:0025109', 'Reduced red cell pyruvate kinase level', 'XPO:0102929', 'abnormal barrier cell morphology', 0.43902439024390244, 5.43643956286526, 1.5449043867452603, 'HP:0025461', 'Abnormal cell morphology'),
(21467, 'HP:0025109', 'Reduced red cell pyruvate kinase level', 'XPO:0102739', 'abnormal erythroid cell morphology', 0.4444444444444444, 5.574066539846944, 1.573964074113079, 'HP:0001871', 'Abnormality of blood and blood-forming tissues'),
(21468, 'HP:0025109', 'Reduced red cell pyruvate kinase level', 'XPO:0101658', 'abnormal germ cell morphology', 0.43902439024390244, 5.43643956286526, 1.5449043867452603, 'HP:0025461', 'Abnormal cell morphology'),
(21469, 'HP:0025109', 'Reduced red cell pyruvate kinase level', 'XPO:0140331', 'abnormally necrotic myeloid cell', 0.40816326530612246, 5.574066539846944, 1.5083531416540121, 'UPHENO:0004459', 'abnormal hematopoietic system'),
(21470, 'HP:0025244', 'Subretinal pigment epithelium hemorrhage', 'XPO:0102939', 'abnormal retinal ganglion cell layer morphology', 0.43, 8.040873045973026, 1.859455675666511, 'HP:0000479', 'Abnormal retinal morphology'),
(21471, 'HP:0025244', 'Subretinal pigment epithelium hemorrhage', 'XPO:0102946', 'abnormal retinal inner nuclear layer morphology', 0.43, 8.040873045973026, 1.859455675666511, 'HP:0000479', 'Abnormal retinal morphology'),
(21472, 'HP:0025244', 'Subretinal pigment epithelium hemorrhage', 'XPO:0101817', 'abnormal eye morphology', 0.40229885057471265, 6.887869297006056, 1.6646266551675757, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(21473, 'HP:0025244', 'Subretinal pigment epithelium hemorrhage', 'XPO:0129780', 'increased size of the retina', 0.46236559139784944, 8.040873045973026, 1.9281657141584967, 'HP:0000479', 'Abnormal retinal morphology'),
(21474, 'HP:0025244', 'Subretinal pigment epithelium hemorrhage', 'XPO:0130413', 'increased size of the central retina', 0.4725274725274725, 8.040873045973026, 1.9492391893577128, 'HP:0000479', 'Abnormal retinal morphology'),
(21475, 'HP:0025244', 'Subretinal pigment epithelium hemorrhage', 'XPO:0103226', 'abnormal retinal outer plexiform layer morphology', 0.43, 8.040873045973026, 1.859455675666511, 'HP:0000479', 'Abnormal retinal morphology'),
(21476, 'HP:0025244', 'Subretinal pigment epithelium hemorrhage', 'XPO:0102805', 'abnormal retinal layer morphology', 0.5119047619047619, 8.040873045973026, 2.028832472656439, 'HP:0000479', 'Abnormal retinal morphology'),
(21477, 'HP:0025244', 'Subretinal pigment epithelium hemorrhage', 'XPO:0129029', 'decreased size of the Muller cell', 0.40186915887850466, 8.040873045973026, 1.797603651429875, 'HP:0000479', 'Abnormal retinal morphology'),
(21478, 'HP:0025244', 'Subretinal pigment epithelium hemorrhage', 'XPO:0101961', 'abnormal retinal blood vessel morphology', 0.44554455445544555, 8.040873045973026, 1.8927670746029088, 'HP:0000479', 'Abnormal retinal morphology'),
(21479, 'HP:0025244', 'Subretinal pigment epithelium hemorrhage', 'XPO:0139887', 'abnormally necrotic Muller cell', 0.43434343434343436, 8.040873045973026, 1.8688232698432123, 'HP:0000479', 'Abnormal retinal morphology'),
(21480, 'HP:0025244', 'Subretinal pigment epithelium hemorrhage', 'XPO:0128787', 'decreased size of the peripheral retina', 0.44329896907216493, 8.040873045973026, 1.8879911895239345, 'HP:0000479', 'Abnormal retinal morphology'),
(21481, 'HP:0025244', 'Subretinal pigment epithelium hemorrhage', 'XPO:0140520', 'abnormally necrotic retinal outer nuclear layer', 0.40186915887850466, 8.040873045973026, 1.797603651429875, 'HP:0000479', 'Abnormal retinal morphology'),
(21482, 'HP:0025244', 'Subretinal pigment epithelium hemorrhage', 'XPO:0130122', 'increased size of the retinal layer', 0.4725274725274725, 8.040873045973026, 1.9492391893577128, 'HP:0000479', 'Abnormal retinal morphology'),
(21483, 'HP:0025244', 'Subretinal pigment epithelium hemorrhage', 'XPO:0102815', 'abnormal retinal ganglion cell morphology', 0.4056603773584906, 8.040873045973026, 1.8060630094548564, 'HP:0000479', 'Abnormal retinal morphology'),
(21484, 'HP:0025244', 'Subretinal pigment epithelium hemorrhage', 'XPO:0128300', 'decreased size of the retina', 0.46236559139784944, 8.040873045973026, 1.9281657141584967, 'HP:0000479', 'Abnormal retinal morphology'),
(21485, 'HP:0025244', 'Subretinal pigment epithelium hemorrhage', 'XPO:0140192', 'abnormally necrotic retina', 0.4725274725274725, 8.040873045973026, 1.9492391893577128, 'HP:0000479', 'Abnormal retinal morphology'),
(21486, 'HP:0025244', 'Subretinal pigment epithelium hemorrhage', 'XPO:0101861', 'abnormal photoreceptor layer morphology', 0.43434343434343436, 8.040873045973026, 1.8688232698432123, 'HP:0000479', 'Abnormal retinal morphology'),
(21487, 'HP:0025244', 'Subretinal pigment epithelium hemorrhage', 'XPO:0140006', 'abnormally necrotic retinal neural layer', 0.40186915887850466, 8.040873045973026, 1.797603651429875, 'HP:0000479', 'Abnormal retinal morphology'),
(21488, 'HP:0025244', 'Subretinal pigment epithelium hemorrhage', 'XPO:0102505', 'abnormal retinal stem cell region morphology', 0.4777777777777778, 8.040873045973026, 1.960038381077836, 'HP:0000479', 'Abnormal retinal morphology'),
(21489, 'HP:0025244', 'Subretinal pigment epithelium hemorrhage', 'XPO:0140391', 'abnormally necrotic central retina', 0.48314606741573035, 8.040873045973026, 1.9710190741722953, 'HP:0000479', 'Abnormal retinal morphology'),
(21490, 'HP:0025244', 'Subretinal pigment epithelium hemorrhage', 'XPO:0140489', 'abnormally necrotic ciliary marginal zone', 0.4215686274509804, 8.040873045973026, 1.8411354685352277, 'HP:0000479', 'Abnormal retinal morphology'),
(21491, 'HP:0025244', 'Subretinal pigment epithelium hemorrhage', 'XPO:0140487', 'abnormally necrotic retinal layer', 0.4777777777777778, 8.040873045973026, 1.960038381077836, 'HP:0000479', 'Abnormal retinal morphology'),
(21492, 'HP:0025244', 'Subretinal pigment epithelium hemorrhage', 'XPO:0140271', 'abnormally necrotic peripheral retina', 0.45263157894736844, 8.040873045973026, 1.9077612698957138, 'HP:0000479', 'Abnormal retinal morphology'),
(21493, 'HP:0025244', 'Subretinal pigment epithelium hemorrhage', 'XPO:0128669', 'decreased size of the ciliary marginal zone', 0.41346153846153844, 8.040873045973026, 1.8233463028623837, 'HP:0000479', 'Abnormal retinal morphology'),
(21494, 'HP:0025244', 'Subretinal pigment epithelium hemorrhage', 'XPO:0103184', 'abnormal inner limiting membrane morphology', 0.43, 8.040873045973026, 1.859455675666511, 'HP:0000479', 'Abnormal retinal morphology'),
(21495, 'HP:0025244', 'Subretinal pigment epithelium hemorrhage', 'XPO:0140553', 'abnormally necrotic retinal stem cell region', 0.46236559139784944, 8.040873045973026, 1.9281657141584967, 'HP:0000479', 'Abnormal retinal morphology'),
(21496, 'HP:0025244', 'Subretinal pigment epithelium hemorrhage', 'XPO:0141014', 'abnormally necrotic retinal outer plexiform layer', 0.40186915887850466, 8.040873045973026, 1.797603651429875, 'HP:0000479', 'Abnormal retinal morphology'),
(21497, 'HP:0025244', 'Subretinal pigment epithelium hemorrhage', 'XPO:0140317', 'abnormally necrotic retinal progenitor cell', 0.41346153846153844, 8.040873045973026, 1.8233463028623837, 'HP:0000479', 'Abnormal retinal morphology'),
(21498, 'HP:0025244', 'Subretinal pigment epithelium hemorrhage', 'XPO:0140531', 'abnormally necrotic retinal progenitor cell region', 0.46236559139784944, 8.040873045973026, 1.9281657141584967, 'HP:0000479', 'Abnormal retinal morphology'),
(21499, 'HP:0025244', 'Subretinal pigment epithelium hemorrhage', 'XPO:0100329', 'abnormal retinal blood vessel', 0.5421686746987951, 8.040873045973026, 2.0879438409010094, 'HP:0000479', 'Abnormal retinal morphology'),
(21500, 'HP:0025244', 'Subretinal pigment epithelium hemorrhage', 'XPO:0128935', 'decreased size of the central retina', 0.4725274725274725, 8.040873045973026, 1.9492391893577128, 'HP:0000479', 'Abnormal retinal morphology'),
(21501, 'HP:0025244', 'Subretinal pigment epithelium hemorrhage', 'XPO:0102017', 'abnormal retinal neural layer morphology', 0.43434343434343436, 8.040873045973026, 1.8688232698432123, 'HP:0000479', 'Abnormal retinal morphology'),
(21502, 'HP:0025244', 'Subretinal pigment epithelium hemorrhage', 'XPO:0102963', 'abnormal retinal outer nuclear layer morphology', 0.43, 8.040873045973026, 1.859455675666511, 'HP:0000479', 'Abnormal retinal morphology'),
(21503, 'HP:0025244', 'Subretinal pigment epithelium hemorrhage', 'XPO:0102581', 'abnormal outer limiting membrane morphology', 0.43, 8.040873045973026, 1.859455675666511, 'HP:0000479', 'Abnormal retinal morphology'),
(21504, 'HP:0025244', 'Subretinal pigment epithelium hemorrhage', 'XPO:0103926', 'decreased pigmentation in the retinal pigmented epithelium', 0.4174757281553398, 8.040873045973026, 1.8321761186829812, 'HP:0000479', 'Abnormal retinal morphology'),
(21505, 'HP:0025244', 'Subretinal pigment epithelium hemorrhage', 'XPO:0129810', 'increased size of the retinal progenitor cell region', 0.45263157894736844, 8.040873045973026, 1.9077612698957138, 'HP:0000479', 'Abnormal retinal morphology'),
(21506, 'HP:0025244', 'Subretinal pigment epithelium hemorrhage', 'XPO:0130265', 'increased size of the peripheral retina', 0.44329896907216493, 8.040873045973026, 1.8879911895239345, 'HP:0000479', 'Abnormal retinal morphology'),
(21507, 'HP:0025244', 'Subretinal pigment epithelium hemorrhage', 'XPO:0130148', 'increased size of the ciliary marginal zone', 0.41346153846153844, 8.040873045973026, 1.8233463028623837, 'HP:0000479', 'Abnormal retinal morphology'),
(21508, 'HP:0025244', 'Subretinal pigment epithelium hemorrhage', 'XPO:0103155', 'abnormal bipolar neuron morphology', 0.40186915887850466, 8.040873045973026, 1.797603651429875, 'HP:0000479', 'Abnormal retinal morphology'),
(21509, 'HP:0025244', 'Subretinal pigment epithelium hemorrhage', 'XPO:0129955', 'increased size of the retinal stem cell region', 0.45263157894736844, 8.040873045973026, 1.9077612698957138, 'HP:0000479', 'Abnormal retinal morphology'),
(21510, 'HP:0025244', 'Subretinal pigment epithelium hemorrhage', 'XPO:0102196', 'abnormal central retina morphology', 0.5, 8.040873045973026, 2.0051026215599324, 'HP:0000479', 'Abnormal retinal morphology'),
(21511, 'HP:0025244', 'Subretinal pigment epithelium hemorrhage', 'XPO:0103186', 'abnormal peripheral retina morphology', 0.48314606741573035, 8.040873045973026, 1.9710190741722953, 'HP:0000479', 'Abnormal retinal morphology'),
(21512, 'HP:0025244', 'Subretinal pigment epithelium hemorrhage', 'XPO:0102756', 'abnormal Muller cell morphology', 0.4574468085106383, 8.040873045973026, 1.9178820903589395, 'HP:0000479', 'Abnormal retinal morphology'),
(21513, 'HP:0025244', 'Subretinal pigment epithelium hemorrhage', 'XPO:0103086', 'abnormal amacrine cell morphology', 0.40186915887850466, 8.040873045973026, 1.797603651429875, 'HP:0000479', 'Abnormal retinal morphology'),
(21514, 'HP:0025244', 'Subretinal pigment epithelium hemorrhage', 'XPO:0141033', 'abnormally necrotic photoreceptor layer', 0.4056603773584906, 8.040873045973026, 1.8060630094548564, 'HP:0000479', 'Abnormal retinal morphology'),
(21515, 'HP:0025244', 'Subretinal pigment epithelium hemorrhage', 'XPO:0102818', 'abnormal optic chiasm morphology', 0.41414141414141414, 7.796308075334707, 1.7968789751681224, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(21516, 'HP:0025244', 'Subretinal pigment epithelium hemorrhage', 'XPO:0102663', 'abnormal retinal progenitor cell morphology', 0.43434343434343436, 8.040873045973026, 1.8688232698432123, 'HP:0000479', 'Abnormal retinal morphology'),
(21517, 'HP:0025244', 'Subretinal pigment epithelium hemorrhage', 'XPO:0102441', 'abnormal retinal inner plexiform layer morphology', 0.43, 8.040873045973026, 1.859455675666511, 'HP:0000479', 'Abnormal retinal morphology'),
(21518, 'HP:0025244', 'Subretinal pigment epithelium hemorrhage', 'XPO:0140948', 'abnormally necrotic retinal inner nuclear layer', 0.40186915887850466, 8.040873045973026, 1.797603651429875, 'HP:0000479', 'Abnormal retinal morphology'),
(21519, 'HP:0025244', 'Subretinal pigment epithelium hemorrhage', 'XPO:0141182', 'abnormally necrotic inner limiting membrane', 0.40186915887850466, 8.040873045973026, 1.797603651429875, 'HP:0000479', 'Abnormal retinal morphology'),
(21520, 'HP:0025244', 'Subretinal pigment epithelium hemorrhage', 'XPO:0100371', 'abnormal hyaloid blood vessel', 0.4074074074074074, 6.887869297006056, 1.6751623720864552, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(21521, 'HP:0025244', 'Subretinal pigment epithelium hemorrhage', 'XPO:0141333', 'increased pigmentation in the retinal pigmented epithelium', 0.4174757281553398, 8.040873045973026, 1.8321761186829812, 'HP:0000479', 'Abnormal retinal morphology'),
(21522, 'HP:0025244', 'Subretinal pigment epithelium hemorrhage', 'XPO:0130506', 'increased size of the Muller cell', 0.40186915887850466, 8.040873045973026, 1.797603651429875, 'HP:0000479', 'Abnormal retinal morphology'),
(21523, 'HP:0025244', 'Subretinal pigment epithelium hemorrhage', 'XPO:0128330', 'decreased size of the retinal progenitor cell region', 0.45263157894736844, 8.040873045973026, 1.9077612698957138, 'HP:0000479', 'Abnormal retinal morphology'),
(21524, 'HP:0025244', 'Subretinal pigment epithelium hemorrhage', 'XPO:0127563', 'abnormally localised retinal blood vessel', 0.4838709677419355, 8.040873045973026, 1.9724971539257066, 'HP:0000479', 'Abnormal retinal morphology'),
(21525, 'HP:0025244', 'Subretinal pigment epithelium hemorrhage', 'XPO:0128779', 'decreased size of the retinal blood vessel', 0.4090909090909091, 8.040873045973026, 1.8136835623288017, 'HP:0000479', 'Abnormal retinal morphology'),
(21526, 'HP:0025244', 'Subretinal pigment epithelium hemorrhage', 'XPO:0128475', 'decreased size of the retinal stem cell region', 0.45263157894736844, 8.040873045973026, 1.9077612698957138, 'HP:0000479', 'Abnormal retinal morphology'),
(21527, 'HP:0025244', 'Subretinal pigment epithelium hemorrhage', 'XPO:0128875', 'decreased size of the photoreceptor layer', 0.40186915887850466, 8.040873045973026, 1.797603651429875, 'HP:0000479', 'Abnormal retinal morphology'),
(21528, 'HP:0025244', 'Subretinal pigment epithelium hemorrhage', 'XPO:0102996', 'abnormal optic fiber layer morphology', 0.43, 8.040873045973026, 1.859455675666511, 'HP:0000479', 'Abnormal retinal morphology'),
(21529, 'HP:0025244', 'Subretinal pigment epithelium hemorrhage', 'XPO:0100779', 'abnormal optic choroid vascular plexus', 0.4024390243902439, 6.887869297006056, 1.6649166345540045, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(21530, 'HP:0025244', 'Subretinal pigment epithelium hemorrhage', 'XPO:0140240', 'abnormally necrotic eye photoreceptor cell', 0.40186915887850466, 8.040873045973026, 1.797603651429875, 'HP:0000479', 'Abnormal retinal morphology'),
(21531, 'HP:0025244', 'Subretinal pigment epithelium hemorrhage', 'XPO:0102117', 'abnormal retina morphology', 0.5, 8.040873045973026, 2.0051026215599324, 'HP:0000479', 'Abnormal retinal morphology'),
(21532, 'HP:0025244', 'Subretinal pigment epithelium hemorrhage', 'XPO:0102450', 'abnormal retinal stem cell morphology', 0.43434343434343436, 8.040873045973026, 1.8688232698432123, 'HP:0000479', 'Abnormal retinal morphology'),
(21533, 'HP:0025244', 'Subretinal pigment epithelium hemorrhage', 'XPO:0130257', 'increased size of the retinal blood vessel', 0.4090909090909091, 8.040873045973026, 1.8136835623288017, 'HP:0000479', 'Abnormal retinal morphology'),
(21534, 'HP:0025244', 'Subretinal pigment epithelium hemorrhage', 'XPO:0102882', 'abnormal retinal cone cell morphology', 0.4095238095238095, 8.040873045973026, 1.8146429295275122, 'HP:0000479', 'Abnormal retinal morphology'),
(21535, 'HP:0025244', 'Subretinal pigment epithelium hemorrhage', 'XPO:0102239', 'abnormal retinal pigmented epithelium morphology', 0.43, 8.040873045973026, 1.859455675666511, 'HP:0000479', 'Abnormal retinal morphology'),
(21536, 'HP:0025244', 'Subretinal pigment epithelium hemorrhage', 'XPO:0141138', 'abnormally necrotic retinal inner plexiform layer', 0.40186915887850466, 8.040873045973026, 1.797603651429875, 'HP:0000479', 'Abnormal retinal morphology'),
(21537, 'HP:0025244', 'Subretinal pigment epithelium hemorrhage', 'XPO:0141156', 'abnormally necrotic outer limiting membrane', 0.40186915887850466, 8.040873045973026, 1.797603651429875, 'HP:0000479', 'Abnormal retinal morphology'),
(21538, 'HP:0025244', 'Subretinal pigment epithelium hemorrhage', 'XPO:0140346', 'abnormally necrotic retinal blood vessel', 0.4166666666666667, 8.040873045973026, 1.8303998932351988, 'HP:0000479', 'Abnormal retinal morphology'),
(21539, 'HP:0025244', 'Subretinal pigment epithelium hemorrhage', 'XPO:0139912', 'abnormally necrotic optic fiber layer', 0.40186915887850466, 8.040873045973026, 1.797603651429875, 'HP:0000479', 'Abnormal retinal morphology'),
(21540, 'HP:0025244', 'Subretinal pigment epithelium hemorrhage', 'XPO:0140439', 'abnormally necrotic retinal stem cell', 0.41346153846153844, 8.040873045973026, 1.8233463028623837, 'HP:0000479', 'Abnormal retinal morphology'),
(21541, 'HP:0025244', 'Subretinal pigment epithelium hemorrhage', 'XPO:0102162', 'abnormal ciliary marginal zone morphology', 0.4574468085106383, 8.040873045973026, 1.9178820903589395, 'HP:0000479', 'Abnormal retinal morphology'),
(21542, 'HP:0025244', 'Subretinal pigment epithelium hemorrhage', 'XPO:0102266', 'abnormal horizontal cell morphology', 0.41346153846153844, 8.040873045973026, 1.8233463028623837, 'HP:0000479', 'Abnormal retinal morphology'),
(21543, 'HP:0025244', 'Subretinal pigment epithelium hemorrhage', 'XPO:0125909', 'absent retinal blood vessel', 0.45918367346938777, 8.040873045973026, 1.921519613001876, 'HP:0000479', 'Abnormal retinal morphology'),
(21544, 'HP:0025244', 'Subretinal pigment epithelium hemorrhage', 'XPO:0130353', 'increased size of the photoreceptor layer', 0.40186915887850466, 8.040873045973026, 1.797603651429875, 'HP:0000479', 'Abnormal retinal morphology'),
(21545, 'HP:0025244', 'Subretinal pigment epithelium hemorrhage', 'XPO:0102851', 'abnormal retinal rod cell morphology', 0.4095238095238095, 8.040873045973026, 1.8146429295275122, 'HP:0000479', 'Abnormal retinal morphology'),
(21546, 'HP:0025244', 'Subretinal pigment epithelium hemorrhage', 'XPO:0128643', 'decreased size of the retinal layer', 0.4725274725274725, 8.040873045973026, 1.9492391893577128, 'HP:0000479', 'Abnormal retinal morphology'),
(21547, 'HP:0025244', 'Subretinal pigment epithelium hemorrhage', 'XPO:0102232', 'abnormal eye photoreceptor cell morphology', 0.4174757281553398, 8.040873045973026, 1.8321761186829812, 'HP:0000479', 'Abnormal retinal morphology'),
(21548, 'HP:0025244', 'Subretinal pigment epithelium hemorrhage', 'XPO:0140945', 'abnormally necrotic retinal ganglion cell layer', 0.40186915887850466, 8.040873045973026, 1.797603651429875, 'HP:0000479', 'Abnormal retinal morphology'),
(21549, 'HP:0025244', 'Subretinal pigment epithelium hemorrhage', 'XPO:0102784', 'abnormal retinal progenitor cell region morphology', 0.4777777777777778, 8.040873045973026, 1.960038381077836, 'HP:0000479', 'Abnormal retinal morphology'),
(21550, 'HP:0009804', 'Tooth agenesis', 'XPO:0115393', 'abnormally decreased volume of oral cavity', 0.4583333333333333, 7.884497199543557, 1.9009807687412648, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(21551, 'HP:0009804', 'Tooth agenesis', 'XPO:0141830', 'increased width of mouth', 0.4177215189873418, 7.884497199543557, 1.8148069171801107, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(21552, 'HP:0009804', 'Tooth agenesis', 'XPO:0103828', 'decreased width of the mouth', 0.4177215189873418, 7.884497199543557, 1.8148069171801107, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(21553, 'HP:0009804', 'Tooth agenesis', 'XPO:0130628', 'increased size of the oral cavity', 0.4714285714285714, 7.884497199543557, 1.9279463818305196, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(21554, 'HP:0009804', 'Tooth agenesis', 'XPO:0128880', 'decreased size of the lower jaw', 0.40476190476190477, 7.312692920701687, 1.7204358504524693, 'UPHENO:0076800', 'abnormal mouth morphology'),
(21555, 'HP:0009804', 'Tooth agenesis', 'XPO:0100027', 'abnormal lower jaw', 0.43333333333333335, 7.0866363731414825, 1.752391440773049, 'HP:0000153', 'Abnormality of the mouth'),
(21556, 'HP:0009804', 'Tooth agenesis', 'XPO:0103096', 'abnormal oral cavity morphology', 0.5076923076923077, 7.884497199543557, 2.000724513327561, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(21557, 'HP:0009804', 'Tooth agenesis', 'XPO:0140626', 'abnormally necrotic tongue', 0.4714285714285714, 7.884497199543557, 1.9279463818305196, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(21558, 'HP:0009804', 'Tooth agenesis', 'XPO:0129152', 'decreased size of the oral cavity', 0.4714285714285714, 7.884497199543557, 1.9279463818305196, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(21559, 'HP:0009804', 'Tooth agenesis', 'XPO:0127750', 'abnormally localised tongue', 0.4925373134328358, 7.884497199543557, 1.970636716503552, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(21560, 'HP:0009804', 'Tooth agenesis', 'XPO:0131611', 'increased size of the roof of mouth', 0.41333333333333333, 7.312692920701687, 1.7385567981969117, 'UPHENO:0076800', 'abnormal mouth morphology'),
(21561, 'HP:0009804', 'Tooth agenesis', 'XPO:0126089', 'absent tongue', 0.5223880597014925, 7.884497199543557, 2.0294746102849897, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(21562, 'HP:0009804', 'Tooth agenesis', 'XPO:0139736', 'abnormally necrotic tooth', 0.4367816091954023, 9.181382707377857, 2.002563135975328, 'UPHENO:0002826', 'abnormal dentition'),
(21563, 'HP:0009804', 'Tooth agenesis', 'XPO:0103735', 'increased size of the mouth', 0.44594594594594594, 7.884497199543557, 1.8751158796081413, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(21564, 'HP:0009804', 'Tooth agenesis', 'XPO:0102279', 'abnormal mouth morphology', 0.47692307692307695, 7.312692920701687, 1.8675095738267717, 'UPHENO:0076800', 'abnormal mouth morphology'),
(21565, 'HP:0009804', 'Tooth agenesis', 'XPO:0141311', 'abnormal roof of mouth morphology', 0.45588235294117646, 7.312692920701687, 1.8258498445999793, 'UPHENO:0076800', 'abnormal mouth morphology'),
(21566, 'HP:0009804', 'Tooth agenesis', 'XPO:0140639', 'abnormally necrotic upper jaw', 0.40476190476190477, 7.312692920701687, 1.7204358504524693, 'UPHENO:0076800', 'abnormal mouth morphology'),
(21567, 'HP:0009804', 'Tooth agenesis', 'XPO:0101816', 'abnormal tooth morphology', 0.4810126582278481, 9.181382707377857, 2.101514049984682, 'UPHENO:0002826', 'abnormal dentition'),
(21568, 'HP:0009804', 'Tooth agenesis', 'XPO:0129585', 'increased size of the tongue', 0.4146341463414634, 7.884497199543557, 1.8080878755371381, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(21569, 'HP:0009804', 'Tooth agenesis', 'XPO:0103352', 'decreased size of the mouth', 0.44594594594594594, 7.884497199543557, 1.8751158796081413, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(21570, 'HP:0009804', 'Tooth agenesis', 'XPO:0131573', 'decreased size of the roof of mouth', 0.41333333333333333, 7.312692920701687, 1.7385567981969117, 'UPHENO:0076800', 'abnormal mouth morphology'),
(21571, 'HP:0009804', 'Tooth agenesis', 'XPO:0102861', 'abnormal cementum morphology', 0.4318181818181818, 9.181382707377857, 1.9911524269319016, 'UPHENO:0002826', 'abnormal dentition'),
(21572, 'HP:0009804', 'Tooth agenesis', 'XPO:0130358', 'increased size of the lower jaw', 0.40476190476190477, 7.312692920701687, 1.7204358504524693, 'UPHENO:0076800', 'abnormal mouth morphology'),
(21573, 'HP:0009804', 'Tooth agenesis', 'XPO:0101659', 'abnormal lower jaw morphology', 0.44155844155844154, 7.312692920701687, 1.7969366404134801, 'UPHENO:0076800', 'abnormal mouth morphology'),
(21574, 'HP:0009804', 'Tooth agenesis', 'XPO:0103199', 'abnormal tongue morphology', 0.5076923076923077, 7.884497199543557, 2.000724513327561, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(21575, 'HP:0009804', 'Tooth agenesis', 'XPO:0140789', 'abnormally necrotic roof of mouth', 0.4246575342465753, 7.312692920701687, 1.7622117195182778, 'UPHENO:0076800', 'abnormal mouth morphology'),
(21576, 'HP:0009804', 'Tooth agenesis', 'XPO:0102890', 'abnormal dentine morphology', 0.4222222222222222, 9.181382707377857, 1.9689042154918968, 'UPHENO:0002826', 'abnormal dentition'),
(21577, 'HP:0009804', 'Tooth agenesis', 'XPO:0101506', 'abnormal upper jaw', 0.43333333333333335, 7.0866363731414825, 1.752391440773049, 'HP:0000153', 'Abnormality of the mouth'),
(21578, 'HP:0009804', 'Tooth agenesis', 'XPO:0140897', 'abnormally necrotic lower jaw', 0.4146341463414634, 7.312692920701687, 1.7412903797564627, 'UPHENO:0076800', 'abnormal mouth morphology'),
(21579, 'HP:0009804', 'Tooth agenesis', 'XPO:0130466', 'increased size of the tooth', 0.4175824175824176, 9.181382707377857, 1.9580561758275088, 'UPHENO:0002826', 'abnormal dentition'),
(21580, 'HP:0009804', 'Tooth agenesis', 'XPO:0126046', 'absent tooth', 0.5542168674698795, 11.802658907487096, 2.5575833608160203, 'HP:0009804', 'Tooth agenesis'),
(21581, 'HP:0009804', 'Tooth agenesis', 'XPO:0103138', 'abnormal upper jaw morphology', 0.43037974683544306, 7.312692920701687, 1.7740447930920258, 'UPHENO:0076800', 'abnormal mouth morphology'),
(21582, 'HP:0009804', 'Tooth agenesis', 'XPO:0115558', 'abnormally incomplete structure of mouth', 0.4696969696969697, 7.312692920701687, 1.8533077740024901, 'UPHENO:0076800', 'abnormal mouth morphology'),
(21583, 'HP:0009804', 'Tooth agenesis', 'XPO:0101567', 'abnormal tongue', 0.5614035087719298, 7.884497199543557, 2.103897429231332, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(21584, 'HP:0009804', 'Tooth agenesis', 'XPO:0128989', 'decreased size of the tooth', 0.4175824175824176, 9.181382707377857, 1.9580561758275088, 'UPHENO:0002826', 'abnormal dentition'),
(21585, 'HP:0009804', 'Tooth agenesis', 'XPO:0128105', 'decreased size of the tongue', 0.4230769230769231, 7.884497199543557, 1.8264032455050843, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(21586, 'HP:0009804', 'Tooth agenesis', 'XPO:0102960', 'abnormal oral epithelium morphology', 0.4189189189189189, 7.312692920701687, 1.7502643836650456, 'UPHENO:0076800', 'abnormal mouth morphology'),
(21587, 'HP:0010204', 'Broad proximal phalanx of toe', 'XPO:0129648', 'increased size of the hindlimb digit 1', 0.42990654205607476, 7.639349617137506, 1.812237947252232, 'HP:0001780', 'Abnormal toe morphology'),
(21588, 'HP:0010204', 'Broad proximal phalanx of toe', 'XPO:0129321', 'decreased size of the hindlimb digit 4', 0.4036697247706422, 7.639349617137506, 1.7560678111555397, 'HP:0001780', 'Abnormal toe morphology'),
(21589, 'HP:0010204', 'Broad proximal phalanx of toe', 'XPO:0128168', 'decreased size of the hindlimb digit 1', 0.4036697247706422, 7.639349617137506, 1.7560678111555397, 'UPHENO:0088132', 'abnormal pedal digit morphology'),
(21590, 'HP:0010204', 'Broad proximal phalanx of toe', 'XPO:0139961', 'abnormally necrotic hindlimb digit', 0.4095238095238095, 7.639349617137506, 1.7687553696015759, 'UPHENO:0088132', 'abnormal pedal digit morphology'),
(21591, 'HP:0010204', 'Broad proximal phalanx of toe', 'XPO:0103436', 'decreased size of the hindlimb digit', 0.41509433962264153, 7.639349617137506, 1.7807444467054143, 'HP:0001780', 'Abnormal toe morphology'),
(21592, 'HP:0010204', 'Broad proximal phalanx of toe', 'XPO:0101809', 'abnormal hindlimb digit morphology', 0.44329896907216493, 7.639349617137506, 1.8402488444932914, 'HP:0001780', 'Abnormal toe morphology'),
(21593, 'HP:0010204', 'Broad proximal phalanx of toe', 'XPO:0130149', 'increased size of the claw primordium', 0.46, 7.639349617137506, 1.8745935089728794, 'UPHENO:0088132', 'abnormal pedal digit morphology'),
(21594, 'HP:0010204', 'Broad proximal phalanx of toe', 'XPO:0128802', 'decreased size of the hindlimb digit 3', 0.4036697247706422, 7.639349617137506, 1.7560678111555397, 'HP:0001780', 'Abnormal toe morphology'),
(21595, 'HP:0010204', 'Broad proximal phalanx of toe', 'XPO:0102880', 'abnormal digit-joint region morphology', 0.40476190476190477, 6.466375519622663, 1.617820284280124, 'UPHENO:0086700', 'abnormal digit morphology'),
(21596, 'HP:0010204', 'Broad proximal phalanx of toe', 'XPO:0101872', 'abnormal hindlimb digit 1 morphology', 0.43434343434343436, 7.639349617137506, 1.8215656312243336, 'UPHENO:0088132', 'abnormal pedal digit morphology'),
(21597, 'HP:0010204', 'Broad proximal phalanx of toe', 'XPO:0102948', 'abnormal hindlimb digit 5 morphology', 0.43434343434343436, 7.639349617137506, 1.8215656312243336, 'HP:0001780', 'Abnormal toe morphology'),
(21598, 'HP:0010204', 'Broad proximal phalanx of toe', 'XPO:0130797', 'increased size of the hindlimb digit 4', 0.42990654205607476, 7.639349617137506, 1.812237947252232, 'UPHENO:0088132', 'abnormal pedal digit morphology'),
(21599, 'HP:0010204', 'Broad proximal phalanx of toe', 'XPO:0128451', 'decreased size of the hindlimb digit 5', 0.4036697247706422, 7.639349617137506, 1.7560678111555397, 'HP:0001780', 'Abnormal toe morphology'),
(21600, 'HP:0010204', 'Broad proximal phalanx of toe', 'XPO:0103759', 'increased size of the hindlimb digit', 0.4423076923076923, 7.639349617137506, 1.838190169674439, 'HP:0001780', 'Abnormal toe morphology'),
(21601, 'HP:0010204', 'Broad proximal phalanx of toe', 'XPO:0133357', 'fused hindlimb digits', 0.4056603773584906, 7.639349617137506, 1.7603924132026476, 'UPHENO:0088132', 'abnormal pedal digit morphology'),
(21602, 'HP:0010204', 'Broad proximal phalanx of toe', 'XPO:0129977', 'increased size of the digit-joint region', 0.42528735632183906, 6.466375519622663, 1.6583328223624414, 'UPHENO:0086700', 'abnormal digit morphology'),
(21603, 'HP:0010204', 'Broad proximal phalanx of toe', 'XPO:0139979', 'abnormally necrotic claw primordium', 0.42574257425742573, 7.639349617137506, 1.8034401491739618, 'HP:0001780', 'Abnormal toe morphology'),
(21604, 'HP:0010204', 'Broad proximal phalanx of toe', 'XPO:0102566', 'abnormal claw primordium morphology', 0.4479166666666667, 7.639349617137506, 1.849808643078929, 'HP:0001780', 'Abnormal toe morphology'),
(21605, 'HP:0010204', 'Broad proximal phalanx of toe', 'XPO:0128272', 'decreased size of the hindlimb digit 2', 0.4036697247706422, 7.639349617137506, 1.7560678111555397, 'UPHENO:0088132', 'abnormal pedal digit morphology'),
(21606, 'HP:0010204', 'Broad proximal phalanx of toe', 'XPO:0129752', 'increased size of the hindlimb digit 2', 0.42990654205607476, 7.639349617137506, 1.812237947252232, 'HP:0001780', 'Abnormal toe morphology'),
(21607, 'HP:0010204', 'Broad proximal phalanx of toe', 'XPO:0130280', 'increased size of the hindlimb digit 3', 0.42990654205607476, 7.639349617137506, 1.812237947252232, 'HP:0001780', 'Abnormal toe morphology'),
(21608, 'HP:0010204', 'Broad proximal phalanx of toe', 'XPO:0141547', 'abnormal hindlimb digit morphology in the regenerating hindlimb', 0.4174757281553398, 7.639349617137506, 1.7858451903924082, 'UPHENO:0088132', 'abnormal pedal digit morphology'),
(21609, 'HP:0010204', 'Broad proximal phalanx of toe', 'XPO:0102051', 'abnormal hindlimb digit 2 morphology', 0.43434343434343436, 7.639349617137506, 1.8215656312243336, 'UPHENO:0088132', 'abnormal pedal digit morphology'),
(21610, 'HP:0010204', 'Broad proximal phalanx of toe', 'XPO:0128670', 'decreased size of the claw primordium', 0.43137254901960786, 7.639349617137506, 1.8153252373050321, 'UPHENO:0088132', 'abnormal pedal digit morphology'),
(21611, 'HP:0010204', 'Broad proximal phalanx of toe', 'XPO:0101810', 'abnormal digit morphology', 0.40476190476190477, 6.466375519622663, 1.617820284280124, 'UPHENO:0086700', 'abnormal digit morphology'),
(21612, 'HP:0010204', 'Broad proximal phalanx of toe', 'XPO:0129693', 'increased size of the digit', 0.4111111111111111, 6.466375519622663, 1.6304596973656729, 'UPHENO:0086700', 'abnormal digit morphology'),
(21613, 'HP:0010204', 'Broad proximal phalanx of toe', 'XPO:0102876', 'abnormal hindlimb digit 4 morphology', 0.43434343434343436, 7.639349617137506, 1.8215656312243336, 'HP:0001780', 'Abnormal toe morphology'),
(21614, 'HP:0010204', 'Broad proximal phalanx of toe', 'XPO:0102180', 'abnormal hindlimb digit 3 morphology', 0.43434343434343436, 7.639349617137506, 1.8215656312243336, 'HP:0001780', 'Abnormal toe morphology'),
(21615, 'HP:0010204', 'Broad proximal phalanx of toe', 'XPO:0129931', 'increased size of the hindlimb digit 5', 0.42990654205607476, 7.639349617137506, 1.812237947252232, 'UPHENO:0088132', 'abnormal pedal digit morphology'),
(21616, 'HP:0011468', 'Facial tics', 'XPO:0100715', 'abnormal ciliated cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(21617, 'HP:0011468', 'Facial tics', 'XPO:0101535', 'abnormal absorptive cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(21618, 'HP:0011468', 'Facial tics', 'XPO:0100006', 'abnormal anatomical structure', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(21619, 'HP:0011468', 'Facial tics', 'XPO:0100852', 'abnormal interdigital region', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(21620, 'HP:0011468', 'Facial tics', 'XPO:0100359', 'abnormal trigeminal placode', 0.42857142857142855, 3.868794716113063, 1.2876547978142938, 'UPHENO:0002844', 'abnormal head'),
(21621, 'HP:0011468', 'Facial tics', 'XPO:0125199', 'absent pharyngeal region', 0.40540540540540543, 3.868794716113063, 1.2523698696136485, 'UPHENO:0002844', 'abnormal head'),
(21622, 'HP:0011468', 'Facial tics', 'XPO:0131672', 'abnormal non-neurogenic ectodermal placode', 0.45454545454545453, 3.868794716113063, 1.3261006948111689, 'UPHENO:0002844', 'abnormal head'),
(21623, 'HP:0011468', 'Facial tics', 'XPO:0100344', 'abnormal portion of organism substance', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(21624, 'HP:0011468', 'Facial tics', 'XPO:0100880', 'abnormal head mesoderm', 0.4411764705882353, 3.868794716113063, 1.306453672460365, 'UPHENO:0002844', 'abnormal head'),
(21625, 'HP:0011468', 'Facial tics', 'XPO:0100099', 'abnormal cranial muscle', 0.40540540540540543, 3.868794716113063, 1.2523698696136485, 'UPHENO:0002844', 'abnormal head'),
(21626, 'HP:0011468', 'Facial tics', 'XPO:0100727', 'abnormal odontogenic papilla', 0.5357142857142857, 3.868794716113063, 1.4396418297332543, 'UPHENO:0002844', 'abnormal head'),
(21627, 'HP:0011468', 'Facial tics', 'XPO:0100940', 'abnormal hatching gland primordium', 0.4838709677419355, 3.868794716113063, 1.3682095757889265, 'UPHENO:0002844', 'abnormal head'),
(21628, 'HP:0011468', 'Facial tics', 'XPO:0100078', 'abnormal neurogenic placode', 0.45454545454545453, 3.868794716113063, 1.3261006948111689, 'UPHENO:0002844', 'abnormal head'),
(21629, 'HP:0011468', 'Facial tics', 'XPO:0101333', 'abnormal barrier epithelial cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(21630, 'HP:0011468', 'Facial tics', 'XPO:0100388', 'abnormal adenohypophyseal placode', 0.42857142857142855, 3.868794716113063, 1.2876547978142938, 'UPHENO:0002844', 'abnormal head'),
(21631, 'HP:0011468', 'Facial tics', 'XPO:0100549', 'abnormal mitotic cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(21632, 'HP:0011468', 'Facial tics', 'XPO:0100754', 'abnormal electrically active cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(21633, 'HP:0011468', 'Facial tics', 'XPO:0101464', 'abnormal oral cavity', 0.4146341463414634, 5.0624614801082695, 1.4488165495297303, 'UPHENO:0002910', 'abnormal face'),
(21634, 'HP:0011468', 'Facial tics', 'XPO:0131656', 'abnormal periocular mesenchyme', 0.46875, 3.868794716113063, 1.346661621632546, 'UPHENO:0002844', 'abnormal head'),
(21635, 'HP:0011468', 'Facial tics', 'XPO:0101173', 'abnormal retinal layer', 0.425, 5.0624614801082695, 1.4668149607384071, 'UPHENO:0002910', 'abnormal face'),
(21636, 'HP:0011468', 'Facial tics', 'XPO:0100691', 'abnormal keratin accumulating cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(21637, 'HP:0011468', 'Facial tics', 'XPO:0100479', 'abnormal lens placode', 0.40540540540540543, 3.868794716113063, 1.2523698696136485, 'UPHENO:0002844', 'abnormal head'),
(21638, 'HP:0011468', 'Facial tics', 'XPO:0100374', 'abnormal pharyngeal endoderm', 0.4411764705882353, 3.868794716113063, 1.306453672460365, 'UPHENO:0002844', 'abnormal head'),
(21639, 'HP:0011468', 'Facial tics', 'XPO:0100460', 'abnormal ethmoid region', 0.40540540540540543, 3.868794716113063, 1.2523698696136485, 'UPHENO:0002844', 'abnormal head'),
(21640, 'HP:0011468', 'Facial tics', 'XPO:0131678', 'abnormal intercanthal region', 0.4838709677419355, 3.868794716113063, 1.3682095757889265, 'UPHENO:0002844', 'abnormal head'),
(21641, 'HP:0011468', 'Facial tics', 'XPO:0101241', 'abnormal nucleate erythrocyte', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(21642, 'HP:0011468', 'Facial tics', 'XPO:0101289', 'abnormal orbital region', 0.4358974358974359, 5.0624614801082695, 1.4855012549670676, 'UPHENO:0002910', 'abnormal face'),
(21643, 'HP:0011468', 'Facial tics', 'XPO:0100172', 'abnormal stem cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(21644, 'HP:0011468', 'Facial tics', 'XPO:0100629', 'abnormal branchial arch 2', 0.4166666666666667, 3.868794716113063, 1.2696447528267278, 'UPHENO:0002844', 'abnormal head'),
(21645, 'HP:0011468', 'Facial tics', 'XPO:0100627', 'abnormal pharyngeal region', 0.5357142857142857, 3.868794716113063, 1.4396418297332543, 'UPHENO:0002844', 'abnormal head'),
(21646, 'HP:0011468', 'Facial tics', 'XPO:0100932', 'abnormal olfactory region', 0.40540540540540543, 3.868794716113063, 1.2523698696136485, 'UPHENO:0002844', 'abnormal head'),
(21647, 'HP:0011468', 'Facial tics', 'XPO:0100481', 'abnormal anatomical line', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(21648, 'HP:0011468', 'Facial tics', 'XPO:0100049', 'abnormal chondrocranium', 0.40540540540540543, 3.868794716113063, 1.2523698696136485, 'UPHENO:0002844', 'abnormal head'),
(21649, 'HP:0011468', 'Facial tics', 'XPO:0101196', 'abnormal occipital region', 0.40540540540540543, 3.868794716113063, 1.2523698696136485, 'UPHENO:0002844', 'abnormal head'),
(21650, 'HP:0011468', 'Facial tics', 'XPO:0126449', 'abnormally localised head region', 0.4166666666666667, 3.868794716113063, 1.2696447528267278, 'UPHENO:0002844', 'abnormal head'),
(21651, 'HP:0011468', 'Facial tics', 'XPO:0100004', 'abnormal cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(21652, 'HP:0011468', 'Facial tics', 'XPO:0101373', 'abnormal oxygen accumulating cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(21653, 'HP:0011468', 'Facial tics', 'XPO:0101469', 'abnormal medial nasal prominence', 0.5, 3.868794716113063, 1.3908261422825396, 'UPHENO:0002844', 'abnormal head'),
(21654, 'HP:0011468', 'Facial tics', 'XPO:0101256', 'abnormal head endoderm', 0.45454545454545453, 3.868794716113063, 1.3261006948111689, 'UPHENO:0002844', 'abnormal head'),
(21655, 'HP:0011468', 'Facial tics', 'XPO:0100132', 'abnormal cranium', 0.4166666666666667, 3.868794716113063, 1.2696447528267278, 'UPHENO:0002844', 'abnormal head'),
(21656, 'HP:0011468', 'Facial tics', 'XPO:0100533', 'abnormal melanoblast', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(21657, 'HP:0011468', 'Facial tics', 'XPO:0100591', 'abnormal pharyngeal arch', 0.4411764705882353, 3.868794716113063, 1.306453672460365, 'UPHENO:0002844', 'abnormal head'),
(21658, 'HP:0011468', 'Facial tics', 'XPO:0101326', 'abnormal cementoblast', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(21659, 'HP:0011468', 'Facial tics', 'XPO:0100592', 'abnormal auditory apparatus', 0.40540540540540543, 3.868794716113063, 1.2523698696136485, 'UPHENO:0002844', 'abnormal head'),
(21660, 'HP:0011468', 'Facial tics', 'XPO:0101402', 'abnormal oropharyngeal papilla', 0.5172413793103449, 3.868794716113063, 1.4146026704452719, 'UPHENO:0002844', 'abnormal head'),
(21661, 'HP:0011468', 'Facial tics', 'XPO:0100647', 'abnormal mouth', 0.425, 5.0624614801082695, 1.4668149607384071, 'UPHENO:0002910', 'abnormal face'),
(21662, 'HP:0011468', 'Facial tics', 'XPO:0101103', 'abnormal pharyngeal mesenchyme', 0.42857142857142855, 3.868794716113063, 1.2876547978142938, 'UPHENO:0002844', 'abnormal head'),
(21663, 'HP:0011468', 'Facial tics', 'XPO:0100704', 'abnormal Merkel cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(21664, 'HP:0011468', 'Facial tics', 'XPO:0100451', 'abnormal head mesenchyme', 0.5, 3.868794716113063, 1.3908261422825396, 'UPHENO:0002844', 'abnormal head'),
(21665, 'HP:0011468', 'Facial tics', 'XPO:0100740', 'abnormal profundal placode', 0.4411764705882353, 3.868794716113063, 1.306453672460365, 'UPHENO:0002844', 'abnormal head'),
(21666, 'HP:0011468', 'Facial tics', 'XPO:0103843', 'abnormally localised head', 0.4166666666666667, 3.868794716113063, 1.2696447528267278, 'UPHENO:0002844', 'abnormal head'),
(21667, 'HP:0011468', 'Facial tics', 'XPO:0100285', 'abnormal progenitor cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(21668, 'HP:0011468', 'Facial tics', 'XPO:0101132', 'abnormal apoptotic cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(21669, 'HP:0011468', 'Facial tics', 'XPO:0100337', 'abnormal zygote', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(21670, 'HP:0011468', 'Facial tics', 'XPO:0131651', 'abnormal roof of mouth', 0.40476190476190477, 5.0624614801082695, 1.4314648271866113, 'UPHENO:0002910', 'abnormal face'),
(21671, 'HP:0011468', 'Facial tics', 'XPO:0127208', 'abnormally localised olfactory pit', 0.4146341463414634, 5.0624614801082695, 1.4488165495297303, 'UPHENO:0002910', 'abnormal face'),
(21672, 'HP:0011468', 'Facial tics', 'XPO:0100664', 'abnormal periocular region', 0.5172413793103449, 3.868794716113063, 1.4146026704452719, 'UPHENO:0002844', 'abnormal head'),
(21673, 'HP:0011468', 'Facial tics', 'XPO:0100580', 'abnormal globe', 0.40476190476190477, 5.0624614801082695, 1.4314648271866113, 'UPHENO:0002910', 'abnormal face'),
(21674, 'HP:0011468', 'Facial tics', 'XPO:0101102', 'abnormal craniofacial region', 0.5, 3.868794716113063, 1.3908261422825396, 'UPHENO:0002844', 'abnormal head'),
(21675, 'HP:0011468', 'Facial tics', 'XPO:0100450', 'abnormal circumpharyngeal ridge', 0.4838709677419355, 3.868794716113063, 1.3682095757889265, 'UPHENO:0002844', 'abnormal head'),
(21676, 'HP:0011468', 'Facial tics', 'XPO:0101520', 'abnormal otic region', 0.40540540540540543, 3.868794716113063, 1.2523698696136485, 'UPHENO:0002844', 'abnormal head'),
(21677, 'HP:0011468', 'Facial tics', 'XPO:0100572', 'abnormal branchial arch', 0.42857142857142855, 3.868794716113063, 1.2876547978142938, 'UPHENO:0002844', 'abnormal head'),
(21678, 'HP:0011468', 'Facial tics', 'XPO:0100893', 'abnormal hyoid arch', 0.42857142857142855, 3.868794716113063, 1.2876547978142938, 'UPHENO:0002844', 'abnormal head'),
(21679, 'HP:0011468', 'Facial tics', 'XPO:0100594', 'abnormal Jacobsons organ', 0.4857142857142857, 5.0624614801082695, 1.5680911522506826, 'UPHENO:0002910', 'abnormal face'),
(21680, 'HP:0011468', 'Facial tics', 'XPO:0101334', 'abnormal olfactory pit', 0.5, 5.0624614801082695, 1.590984204841184, 'UPHENO:0002910', 'abnormal face'),
(21681, 'HP:0011468', 'Facial tics', 'XPO:0100906', 'abnormal lateral nasal prominence', 0.5, 3.868794716113063, 1.3908261422825396, 'UPHENO:0002844', 'abnormal head'),
(21682, 'HP:0011468', 'Facial tics', 'XPO:0101237', 'abnormal mucus secreting cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(21683, 'HP:0011468', 'Facial tics', 'XPO:0100788', 'abnormal branchial arch 4', 0.4166666666666667, 3.868794716113063, 1.2696447528267278, 'UPHENO:0002844', 'abnormal head'),
(21684, 'HP:0011468', 'Facial tics', 'XPO:0126822', 'abnormally localised pharyngeal region', 0.42857142857142855, 3.868794716113063, 1.2876547978142938, 'UPHENO:0002844', 'abnormal head'),
(21685, 'HP:0011468', 'Facial tics', 'XPO:0101467', 'abnormal alkali secreting cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(21686, 'HP:0011468', 'Facial tics', 'XPO:0115812', 'duplicated head', 0.42857142857142855, 3.868794716113063, 1.2876547978142938, 'UPHENO:0002844', 'abnormal head'),
(21687, 'HP:0011468', 'Facial tics', 'XPO:0100373', 'abnormal splanchnocranium', 0.40540540540540543, 3.868794716113063, 1.2523698696136485, 'UPHENO:0002844', 'abnormal head'),
(21688, 'HP:0011468', 'Facial tics', 'XPO:0142052', 'abnormal nasal region', 0.5555555555555556, 3.868794716113063, 1.4660594796394144, 'UPHENO:0002844', 'abnormal head'),
(21689, 'HP:0011468', 'Facial tics', 'XPO:0100661', 'abnormal gill primordium', 0.40540540540540543, 3.868794716113063, 1.2523698696136485, 'UPHENO:0002844', 'abnormal head'),
(21690, 'HP:0011468', 'Facial tics', 'XPO:0100389', 'abnormal cranial placode', 0.46875, 3.868794716113063, 1.346661621632546, 'UPHENO:0002844', 'abnormal head'),
(21691, 'HP:0011468', 'Facial tics', 'XPO:0100625', 'abnormal dorsolateral placode region', 0.4411764705882353, 3.868794716113063, 1.306453672460365, 'UPHENO:0002844', 'abnormal head'),
(21692, 'HP:0011468', 'Facial tics', 'XPO:0101088', 'abnormal dermatocranium', 0.40540540540540543, 3.868794716113063, 1.2523698696136485, 'UPHENO:0002844', 'abnormal head'),
(21693, 'HP:0011468', 'Facial tics', 'XPO:0100719', 'abnormal sphenoid region', 0.40540540540540543, 3.868794716113063, 1.2523698696136485, 'UPHENO:0002844', 'abnormal head'),
(21694, 'HP:0011468', 'Facial tics', 'XPO:0101172', 'abnormal pharyngeal pouch', 0.5, 3.868794716113063, 1.3908261422825396, 'UPHENO:0002844', 'abnormal head'),
(21695, 'HP:0011468', 'Facial tics', 'XPO:0100687', 'abnormal periotic region', 0.5172413793103449, 3.868794716113063, 1.4146026704452719, 'UPHENO:0002844', 'abnormal head'),
(21696, 'HP:0011468', 'Facial tics', 'XPO:0101004', 'abnormal acid secreting cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(21697, 'HP:0011468', 'Facial tics', 'XPO:0101435', 'abnormal paracrine cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(21698, 'HP:0011468', 'Facial tics', 'XPO:0101448', 'abnormal myelin accumulating cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(21699, 'HP:0011468', 'Facial tics', 'XPO:0102259', 'abnormal pharyngeal region morphology', 0.4166666666666667, 3.868794716113063, 1.2696447528267278, 'UPHENO:0002844', 'abnormal head'),
(21700, 'HP:0011468', 'Facial tics', 'XPO:0100769', 'abnormal neurocranium', 0.40540540540540543, 3.868794716113063, 1.2523698696136485, 'UPHENO:0002844', 'abnormal head'),
(21701, 'HP:0011468', 'Facial tics', 'XPO:0100169', 'abnormal brain', 0.40540540540540543, 3.868794716113063, 1.2523698696136485, 'UPHENO:0002844', 'abnormal head'),
(21702, 'HP:0011468', 'Facial tics', 'XPO:0100002', 'abnormal head', 0.5555555555555556, 3.868794716113063, 1.4660594796394144, 'UPHENO:0002844', 'abnormal head'),
(21703, 'HP:0011468', 'Facial tics', 'XPO:0100477', 'abnormal pericyte', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(21704, 'HP:0011468', 'Facial tics', 'XPO:0100289', 'abnormal chondroblast', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(21705, 'HP:0011468', 'Facial tics', 'XPO:0100081', 'abnormal anatomical entity in vitro', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(21706, 'HP:0011468', 'Facial tics', 'XPO:0101634', 'abnormal head morphology', 0.40540540540540543, 3.868794716113063, 1.2523698696136485, 'UPHENO:0002844', 'abnormal head'),
(21707, 'HP:0011468', 'Facial tics', 'XPO:0101297', 'abnormal barrier cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(21708, 'HP:0011468', 'Facial tics', 'XPO:0100638', 'abnormal polar body', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(21709, 'HP:0011468', 'Facial tics', 'XPO:0100571', 'abnormal branchial arch 1', 0.4166666666666667, 3.868794716113063, 1.2696447528267278, 'UPHENO:0002844', 'abnormal head'),
(21710, 'HP:0011468', 'Facial tics', 'XPO:0100108', 'abnormal cell part', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(21711, 'HP:0011468', 'Facial tics', 'XPO:0100791', 'abnormal multiciliated cell precursor', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(21712, 'HP:0011468', 'Facial tics', 'XPO:0100653', 'abnormal myoblast', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(21713, 'HP:0011468', 'Facial tics', 'XPO:0100802', 'abnormal exocrine cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(21714, 'HP:0011468', 'Facial tics', 'XPO:0100185', 'abnormal eye', 0.4146341463414634, 5.0624614801082695, 1.4488165495297303, 'UPHENO:0002910', 'abnormal face'),
(21715, 'HP:0011468', 'Facial tics', 'XPO:0100813', 'abnormal branchial arch 3', 0.4166666666666667, 3.868794716113063, 1.2696447528267278, 'UPHENO:0002844', 'abnormal head'),
(21716, 'HP:0011468', 'Facial tics', 'XPO:0100026', 'abnormal germ cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(21717, 'HP:0011468', 'Facial tics', 'XPO:0101199', 'abnormal optic disc', 0.40476190476190477, 5.0624614801082695, 1.4314648271866113, 'UPHENO:0002910', 'abnormal face'),
(21718, 'HP:0000691', 'Microdontia', 'XPO:0128238', 'decreased size of the ethmoid region', 0.4084507042253521, 5.653868323764771, 1.5196468334580675, 'UPHENO:0012541', 'decreased size of the anatomical entity in the independent continuant'),
(21719, 'HP:0000691', 'Microdontia', 'XPO:0103828', 'decreased width of the mouth', 0.4935064935064935, 7.884497199543557, 1.9725746034075642, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(21720, 'HP:0000691', 'Microdontia', 'XPO:0130466', 'increased size of the tooth', 0.5348837209302325, 9.872199840740173, 2.2979292818931465, 'HP:0006482', 'Abnormal dental morphology'),
(21721, 'HP:0000691', 'Microdontia', 'XPO:0128566', 'decreased size of the palatoquadrate', 0.4268292682926829, 5.725717590856133, 1.5632990276193697, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(21722, 'HP:0000691', 'Microdontia', 'XPO:0101659', 'abnormal lower jaw morphology', 0.5, 7.312692920701687, 1.9121575406725366, 'UPHENO:0076800', 'abnormal mouth morphology'),
(21723, 'HP:0000691', 'Microdontia', 'XPO:0130628', 'increased size of the oral cavity', 0.5142857142857142, 7.884497199543557, 2.0136743217439537, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(21724, 'HP:0000691', 'Microdontia', 'XPO:0128653', 'decreased size of the oral epithelium', 0.4444444444444444, 7.312692920701687, 1.8027994182753895, 'UPHENO:0076800', 'abnormal mouth morphology'),
(21725, 'HP:0000691', 'Microdontia', 'XPO:0102103', 'abnormal mandibular arch morphology', 0.42105263157894735, 5.725717590856133, 1.5526842754751673, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(21726, 'HP:0000691', 'Microdontia', 'XPO:0130132', 'increased size of the oral epithelium', 0.40963855421686746, 7.312692920701687, 1.7307688914087174, 'UPHENO:0076800', 'abnormal mouth morphology'),
(21727, 'HP:0000691', 'Microdontia', 'XPO:0103199', 'abnormal tongue morphology', 0.5303030303030303, 7.884497199543557, 2.044791617092975, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(21728, 'HP:0000691', 'Microdontia', 'XPO:0129307', 'decreased size of the ventral hyoid arch skeleton', 0.4117647058823529, 5.725717590856133, 1.5354635846428564, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(21729, 'HP:0000691', 'Microdontia', 'XPO:0103324', 'decreased size of the branchial arch', 0.40540540540540543, 5.725717590856133, 1.5235605866383823, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(21730, 'HP:0000691', 'Microdontia', 'XPO:0129406', 'decreased size of the suspensorium', 0.4027777777777778, 5.653868323764771, 1.5090568310352477, 'UPHENO:0012541', 'decreased size of the anatomical entity in the independent continuant'),
(21731, 'HP:0000691', 'Microdontia', 'XPO:0126089', 'absent tongue', 0.4583333333333333, 7.884497199543557, 1.9009807687412648, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(21732, 'HP:0000691', 'Microdontia', 'XPO:0103735', 'increased size of the mouth', 0.4864864864864865, 7.884497199543557, 1.9584946618049506, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(21733, 'HP:0000691', 'Microdontia', 'XPO:0103352', 'decreased size of the mouth', 0.5277777777777778, 7.884497199543557, 2.0399172558881427, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(21734, 'HP:0000691', 'Microdontia', 'XPO:0127750', 'abnormally localised tongue', 0.4714285714285714, 7.884497199543557, 1.9279463818305196, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(21735, 'HP:0000691', 'Microdontia', 'XPO:0102890', 'abnormal dentine morphology', 0.5232558139534884, 9.872199840740173, 2.272814546587116, 'HP:0006482', 'Abnormal dental morphology'),
(21736, 'HP:0000691', 'Microdontia', 'XPO:0141009', 'abnormally necrotic oral epithelium', 0.4024390243902439, 7.312692920701687, 1.7154920590526295, 'UPHENO:0076800', 'abnormal mouth morphology'),
(21737, 'HP:0000691', 'Microdontia', 'XPO:0140897', 'abnormally necrotic lower jaw', 0.4691358024691358, 7.312692920701687, 1.8522003297601892, 'UPHENO:0076800', 'abnormal mouth morphology'),
(21738, 'HP:0000691', 'Microdontia', 'XPO:0115558', 'abnormally incomplete structure of mouth', 0.4925373134328358, 7.312692920701687, 1.8978340615348135, 'UPHENO:0076800', 'abnormal mouth morphology'),
(21739, 'HP:0000691', 'Microdontia', 'XPO:0139736', 'abnormally necrotic tooth', 0.5421686746987951, 9.872199840740173, 2.3135249088816305, 'HP:0006482', 'Abnormal dental morphology'),
(21740, 'HP:0000691', 'Microdontia', 'XPO:0128880', 'decreased size of the lower jaw', 0.5125, 7.312692920701687, 1.9359119612884297, 'UPHENO:0076800', 'abnormal mouth morphology'),
(21741, 'HP:0000691', 'Microdontia', 'XPO:0141311', 'abnormal roof of mouth morphology', 0.4782608695652174, 7.312692920701687, 1.8701269676463677, 'UPHENO:0076800', 'abnormal mouth morphology'),
(21742, 'HP:0000691', 'Microdontia', 'XPO:0128105', 'decreased size of the tongue', 0.5, 7.884497199543557, 1.9855096574360394, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(21743, 'HP:0000691', 'Microdontia', 'XPO:0130358', 'increased size of the lower jaw', 0.47560975609756095, 7.312692920701687, 1.8649364858973858, 'UPHENO:0076800', 'abnormal mouth morphology'),
(21744, 'HP:0000691', 'Microdontia', 'XPO:0128989', 'decreased size of the tooth', 0.5903614457831325, 13.511610125483706, 2.824311188332223, 'HP:0000691', 'Microdontia'),
(21745, 'HP:0000691', 'Microdontia', 'XPO:0129252', 'decreased size of the dorsal hyoid arch skeleton', 0.4117647058823529, 5.725717590856133, 1.5354635846428564, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(21746, 'HP:0000691', 'Microdontia', 'XPO:0140639', 'abnormally necrotic upper jaw', 0.4578313253012048, 7.312692920701687, 1.8297485869390886, 'UPHENO:0076800', 'abnormal mouth morphology'),
(21747, 'HP:0000691', 'Microdontia', 'XPO:0102223', 'abnormal pharyngeal arch morphology', 0.4090909090909091, 5.725717590856133, 1.5304701939081158, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(21748, 'HP:0000691', 'Microdontia', 'XPO:0129990', 'increased size of the cementum', 0.4946236559139785, 9.872199840740173, 2.209756451996532, 'HP:0006482', 'Abnormal dental morphology'),
(21749, 'HP:0000691', 'Microdontia', 'XPO:0128668', 'decreased size of the fenestra basicranialis', 0.42028985507246375, 5.653868323764771, 1.541513379245827, 'UPHENO:0012541', 'decreased size of the anatomical entity in the independent continuant'),
(21750, 'HP:0000691', 'Microdontia', 'XPO:0100027', 'abnormal lower jaw', 0.4126984126984127, 7.0866363731414825, 1.7101589348848036, 'HP:0000153', 'Abnormality of the mouth'),
(21751, 'HP:0000691', 'Microdontia', 'XPO:0102960', 'abnormal oral epithelium morphology', 0.44, 7.312692920701687, 1.7937627728071353, 'UPHENO:0076800', 'abnormal mouth morphology'),
(21752, 'HP:0000691', 'Microdontia', 'XPO:0103347', 'decreased size of the hyoid arch skeleton', 0.4166666666666667, 5.725717590856133, 1.5445762081738545, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(21753, 'HP:0000691', 'Microdontia', 'XPO:0130923', 'increased size of the dentine', 0.4791666666666667, 9.872199840740173, 2.174954962833637, 'HP:0006482', 'Abnormal dental morphology'),
(21754, 'HP:0000691', 'Microdontia', 'XPO:0126046', 'absent tooth', 0.40425531914893614, 9.181382707377857, 1.9265572393779424, 'UPHENO:0002826', 'abnormal dentition'),
(21755, 'HP:0000691', 'Microdontia', 'XPO:0103325', 'decreased size of the branchial arch skeleton', 0.42168674698795183, 5.725717590856133, 1.5538530255657437, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(21756, 'HP:0000691', 'Microdontia', 'XPO:0130701', 'increased size of the upper jaw', 0.4642857142857143, 7.312692920701687, 1.8426011114834564, 'UPHENO:0076800', 'abnormal mouth morphology'),
(21757, 'HP:0000691', 'Microdontia', 'XPO:0129585', 'increased size of the tongue', 0.45121951219512196, 7.884497199543557, 1.8861704536658, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(21758, 'HP:0000691', 'Microdontia', 'XPO:0128971', 'decreased size of the fenestra subocularis', 0.42028985507246375, 5.653868323764771, 1.541513379245827, 'UPHENO:0012541', 'decreased size of the anatomical entity in the independent continuant'),
(21759, 'HP:0000691', 'Microdontia', 'XPO:0129152', 'decreased size of the oral cavity', 0.5588235294117647, 7.884497199543557, 2.099057539155634, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(21760, 'HP:0000691', 'Microdontia', 'XPO:0103138', 'abnormal upper jaw morphology', 0.48717948717948717, 7.312692920701687, 1.8874835064202586, 'UPHENO:0076800', 'abnormal mouth morphology'),
(21761, 'HP:0000691', 'Microdontia', 'XPO:0140626', 'abnormally necrotic tongue', 0.49295774647887325, 7.884497199543557, 1.971477611236298, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(21762, 'HP:0000691', 'Microdontia', 'XPO:0101816', 'abnormal tooth morphology', 0.6, 9.872199840740173, 2.433787152658199, 'HP:0006482', 'Abnormal dental morphology'),
(21763, 'HP:0000691', 'Microdontia', 'XPO:0128034', 'decreased size of the cranium', 0.4142857142857143, 5.653868323764771, 1.5304629616518861, 'UPHENO:0012541', 'decreased size of the anatomical entity in the independent continuant'),
(21764, 'HP:0000691', 'Microdontia', 'XPO:0129449', 'decreased size of the dentine', 0.5106382978723404, 9.872199840740173, 2.2452446020269488, 'HP:0006482', 'Abnormal dental morphology'),
(21765, 'HP:0000691', 'Microdontia', 'XPO:0102823', 'abnormal palatoquadrate morphology', 0.41025641025641024, 5.725717590856133, 1.5326488002692003, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(21766, 'HP:0000691', 'Microdontia', 'XPO:0140890', 'abnormally necrotic dentine', 0.47368421052631576, 9.872199840740173, 2.1624766328723712, 'HP:0006482', 'Abnormal dental morphology'),
(21767, 'HP:0000691', 'Microdontia', 'XPO:0129225', 'decreased size of the upper jaw', 0.5, 7.312692920701687, 1.9121575406725366, 'UPHENO:0076800', 'abnormal mouth morphology'),
(21768, 'HP:0000691', 'Microdontia', 'XPO:0128483', 'decreased size of the branchial arch skeleton 3', 0.40229885057471265, 5.725717590856133, 1.517711963949957, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(21769, 'HP:0000691', 'Microdontia', 'XPO:0101567', 'abnormal tongue', 0.5333333333333333, 7.884497199543557, 2.0506255565290066, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(21770, 'HP:0000691', 'Microdontia', 'XPO:0103357', 'decreased size of the pharyngeal arch', 0.4225352112676056, 5.725717590856133, 1.5554154724417018, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(21771, 'HP:0000691', 'Microdontia', 'XPO:0131611', 'increased size of the roof of mouth', 0.4533333333333333, 7.312692920701687, 1.8207381627748578, 'UPHENO:0076800', 'abnormal mouth morphology'),
(21772, 'HP:0000691', 'Microdontia', 'XPO:0102552', 'abnormal branchial arch skeleton morphology', 0.41025641025641024, 5.725717590856133, 1.5326488002692003, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(21773, 'HP:0000691', 'Microdontia', 'XPO:0141830', 'increased width of mouth', 0.45569620253164556, 7.884497199543557, 1.8955040049293994, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(21774, 'HP:0000691', 'Microdontia', 'XPO:0102861', 'abnormal cementum morphology', 0.5357142857142857, 9.872199840740173, 2.2997126964277097, 'HP:0006482', 'Abnormal dental morphology'),
(21775, 'HP:0000691', 'Microdontia', 'XPO:0140789', 'abnormally necrotic roof of mouth', 0.44594594594594594, 7.312692920701687, 1.8058421198805104, 'UPHENO:0076800', 'abnormal mouth morphology'),
(21776, 'HP:0000691', 'Microdontia', 'XPO:0103349', 'decreased size of the mandibular arch', 0.42168674698795183, 5.725717590856133, 1.5538530255657437, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(21777, 'HP:0000691', 'Microdontia', 'XPO:0115393', 'abnormally decreased volume of oral cavity', 0.5428571428571428, 7.884497199543557, 2.0688536977295806, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(21778, 'HP:0000691', 'Microdontia', 'XPO:0102563', 'abnormal hyoid arch skeleton morphology', 0.4050632911392405, 5.725717590856133, 1.5229175983900207, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(21779, 'HP:0000691', 'Microdontia', 'XPO:0103096', 'abnormal oral cavity morphology', 0.5303030303030303, 7.884497199543557, 2.044791617092975, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(21780, 'HP:0000691', 'Microdontia', 'XPO:0131573', 'decreased size of the roof of mouth', 0.4931506849315068, 7.312692920701687, 1.8990154087152158, 'UPHENO:0076800', 'abnormal mouth morphology'),
(21781, 'HP:0000691', 'Microdontia', 'XPO:0102279', 'abnormal mouth morphology', 0.5, 7.312692920701687, 1.9121575406725366, 'UPHENO:0076800', 'abnormal mouth morphology'),
(21782, 'HP:0000691', 'Microdontia', 'XPO:0141006', 'abnormally necrotic cementum', 0.4891304347826087, 9.872199840740173, 2.197451569514569, 'HP:0006482', 'Abnormal dental morphology'),
(21783, 'HP:0000691', 'Microdontia', 'XPO:0101506', 'abnormal upper jaw', 0.4126984126984127, 7.0866363731414825, 1.7101589348848036, 'HP:0000153', 'Abnormality of the mouth'),
(21784, 'HP:0000691', 'Microdontia', 'XPO:0128510', 'decreased size of the cementum', 0.5274725274725275, 9.872199840740173, 2.281954031462751, 'HP:0006482', 'Abnormal dental morphology'),
(21785, 'HP:0100752', 'Abnormal liver lobulation', 'XPO:0103009', 'abnormal manicotto glandulare morphology', 0.40384615384615385, 5.725717590856133, 1.520627839767678, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(21786, 'HP:0100752', 'Abnormal liver lobulation', 'XPO:0140793', 'abnormally necrotic hepatic portal vein', 0.40229885057471265, 10.01729298920255, 2.0074724046487695, 'UPHENO:0019492', 'abnormal liver morphology'),
(21787, 'HP:0100752', 'Abnormal liver lobulation', 'XPO:0141125', 'abnormally necrotic liver parenchyme', 0.5588235294117647, 14.404694921567193, 2.83719623152328, 'UPHENO:0019417', 'abnormal liver parenchyma morphology'),
(21788, 'HP:0100752', 'Abnormal liver lobulation', 'XPO:0102118', 'abnormal oral evagination morphology', 0.40384615384615385, 5.725717590856133, 1.520627839767678, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(21789, 'HP:0100752', 'Abnormal liver lobulation', 'XPO:0126004', 'absent hepatic portal vein', 0.40229885057471265, 10.01729298920255, 2.0074724046487695, 'UPHENO:0019492', 'abnormal liver morphology'),
(21790, 'HP:0100752', 'Abnormal liver lobulation', 'XPO:0115392', 'abnormally incomplete structure of alimentary system', 0.42, 5.725717590856133, 1.5507422055775666, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(21791, 'HP:0100752', 'Abnormal liver lobulation', 'XPO:0100042', 'abnormal hepatic vein', 0.5555555555555556, 10.01729298920255, 2.3590597219611027, 'UPHENO:0019492', 'abnormal liver morphology'),
(21792, 'HP:0100752', 'Abnormal liver lobulation', 'XPO:0130151', 'increased size of the liver', 0.4069767441860465, 10.01729298920255, 2.019110023327942, 'UPHENO:0019492', 'abnormal liver morphology'),
(21793, 'HP:0100752', 'Abnormal liver lobulation', 'XPO:0141833', 'edematous alimentary system', 0.4117647058823529, 5.725717590856133, 1.5354635846428564, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(21794, 'HP:0100752', 'Abnormal liver lobulation', 'XPO:0140645', 'abnormally necrotic hepatic vein', 0.40229885057471265, 10.01729298920255, 2.0074724046487695, 'UPHENO:0019492', 'abnormal liver morphology'),
(21795, 'HP:0100752', 'Abnormal liver lobulation', 'XPO:0102825', 'abnormal bile duct morphology', 0.4426229508196721, 8.69832224767236, 1.9621613237563171, 'UPHENO:0087100', 'abnormal hepatobiliary system morphology'),
(21796, 'HP:0100752', 'Abnormal liver lobulation', 'XPO:0141005', 'abnormally necrotic bile duct', 0.40298507462686567, 8.69832224767236, 1.872243050489645, 'UPHENO:0087100', 'abnormal hepatobiliary system morphology'),
(21797, 'HP:0100752', 'Abnormal liver lobulation', 'XPO:0140908', 'abnormally necrotic hepatocyte', 0.44, 9.184143847054914, 2.010229661681511, 'UPHENO:0086622', 'abnormal liver morphology'),
(21798, 'HP:0100752', 'Abnormal liver lobulation', 'XPO:0102522', 'abnormal pharyngeal cavity morphology', 0.42857142857142855, 5.725717590856133, 1.5664861849086864, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(21799, 'HP:0100752', 'Abnormal liver lobulation', 'XPO:0141647', 'neoplastic liver', 0.5072463768115942, 10.01729298920255, 2.2541596159618282, 'UPHENO:0019492', 'abnormal liver morphology'),
(21800, 'HP:0100752', 'Abnormal liver lobulation', 'XPO:0102763', 'abnormal hepatocyte morphology', 0.4714285714285714, 9.184143847054914, 2.0807853838422647, 'UPHENO:0086622', 'abnormal liver morphology'),
(21801, 'HP:0100752', 'Abnormal liver lobulation', 'XPO:0130724', 'increased size of the liver parenchyme', 0.5428571428571428, 14.404694921567193, 2.796371135749109, 'UPHENO:0019417', 'abnormal liver parenchyma morphology'),
(21802, 'HP:0100752', 'Abnormal liver lobulation', 'XPO:0127068', 'abnormally localised hepatic vein', 0.4794520547945205, 10.01729298920255, 2.191531817508454, 'UPHENO:0019492', 'abnormal liver morphology'),
(21803, 'HP:0100752', 'Abnormal liver lobulation', 'XPO:0130806', 'increased size of the biliary tree', 0.40298507462686567, 8.69832224767236, 1.872243050489645, 'UPHENO:0087100', 'abnormal hepatobiliary system morphology'),
(21804, 'HP:0100752', 'Abnormal liver lobulation', 'XPO:0102426', 'abnormal liver morphology', 0.5303030303030303, 10.01729298920255, 2.304821213805403, 'UPHENO:0019492', 'abnormal liver morphology'),
(21805, 'HP:0100752', 'Abnormal liver lobulation', 'XPO:0107375', 'abnormal larval alimentary system morphology', 0.4117647058823529, 5.725717590856133, 1.5354635846428564, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(21806, 'HP:0100752', 'Abnormal liver lobulation', 'XPO:0101784', 'abnormal alimentary system morphology', 0.42857142857142855, 5.725717590856133, 1.5664861849086864, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(21807, 'HP:0100752', 'Abnormal liver lobulation', 'XPO:0129248', 'decreased size of the liver parenchyme', 0.5428571428571428, 14.404694921567193, 2.796371135749109, 'UPHENO:0019417', 'abnormal liver parenchyma morphology'),
(21808, 'HP:0100752', 'Abnormal liver lobulation', 'XPO:0139877', 'abnormally necrotic liver', 0.45454545454545453, 10.01729298920255, 2.133849806123212, 'UPHENO:0019492', 'abnormal liver morphology'),
(21809, 'HP:0100752', 'Abnormal liver lobulation', 'XPO:0102211', 'abnormal biliary tree morphology', 0.45, 8.69832224767236, 1.9784450994284786, 'UPHENO:0087100', 'abnormal hepatobiliary system morphology'),
(21810, 'HP:0100752', 'Abnormal liver lobulation', 'XPO:0128672', 'decreased size of the liver', 0.4375, 10.01729298920255, 2.0934578292328023, 'UPHENO:0019492', 'abnormal liver morphology'),
(21811, 'HP:0100752', 'Abnormal liver lobulation', 'XPO:0101787', 'abnormal hepatic portal vein morphology', 0.4375, 10.01729298920255, 2.0934578292328023, 'UPHENO:0019492', 'abnormal liver morphology'),
(21812, 'HP:0100752', 'Abnormal liver lobulation', 'XPO:0125433', 'absent hepatic vein', 0.4605263157894737, 10.01729298920255, 2.147842413796034, 'UPHENO:0019492', 'abnormal liver morphology'),
(21813, 'HP:0100752', 'Abnormal liver lobulation', 'XPO:0102125', 'abnormal liver and biliary system morphology', 0.44, 8.69832224767236, 1.9563388737577747, 'UPHENO:0087100', 'abnormal hepatobiliary system morphology'),
(21814, 'HP:0100752', 'Abnormal liver lobulation', 'XPO:0142061', 'abnormal digestive tract morphology', 0.4117647058823529, 5.725717590856133, 1.5354635846428564, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(21815, 'HP:0100752', 'Abnormal liver lobulation', 'XPO:0129330', 'decreased size of the biliary tree', 0.40298507462686567, 8.69832224767236, 1.872243050489645, 'UPHENO:0087100', 'abnormal hepatobiliary system morphology'),
(21816, 'HP:0100752', 'Abnormal liver lobulation', 'XPO:0103168', 'abnormal liver parenchyme morphology', 0.6031746031746031, 14.404694921567193, 2.947633990706362, 'UPHENO:0019417', 'abnormal liver parenchyma morphology'),
(21817, 'HP:0100752', 'Abnormal liver lobulation', 'XPO:0103088', 'abnormal capillary system of liver morphology', 0.4024390243902439, 9.184143847054914, 1.9225134302959865, 'UPHENO:0086622', 'abnormal liver morphology'),
(21818, 'HP:0100752', 'Abnormal liver lobulation', 'XPO:0140388', 'abnormally necrotic biliary tree', 0.4153846153846154, 8.69832224767236, 1.900828567057226, 'UPHENO:0087100', 'abnormal hepatobiliary system morphology'),
(21819, 'HP:0100752', 'Abnormal liver lobulation', 'XPO:0101674', 'abnormal hepatic vein morphology', 0.4375, 10.01729298920255, 2.0934578292328023, 'UPHENO:0019492', 'abnormal liver morphology'),
(21820, 'HP:0100752', 'Abnormal liver lobulation', 'XPO:0101820', 'abnormal delta cell morphology', 0.423728813559322, 7.428233084304616, 1.7741353927066836, 'UPHENO:0076812', 'abnormal endocrine system morphology'),
(21821, 'HP:0007057', 'Poor hand-eye coordination', 'XPO:0100032', 'abnormal nervous system', 0.4482758620689655, 3.94131651835137, 1.3292091859262085, 'UPHENO:0004523', 'abnormal nervous system'),
(21822, 'HP:0007057', 'Poor hand-eye coordination', 'XPO:0100587', 'abnormal vestibuloauditory system', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(21823, 'HP:0007057', 'Poor hand-eye coordination', 'XPO:0107253', 'abnormal enteric nervous system', 0.43333333333333335, 3.94131651835137, 1.3068679445984308, 'UPHENO:0004523', 'abnormal nervous system'),
(21824, 'HP:0007057', 'Poor hand-eye coordination', 'XPO:0100642', 'abnormal gustatory system', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(21825, 'HP:0007057', 'Poor hand-eye coordination', 'XPO:0100274', 'abnormal sensory system', 0.43333333333333335, 3.94131651835137, 1.3068679445984308, 'UPHENO:0004523', 'abnormal nervous system'),
(21826, 'HP:0007057', 'Poor hand-eye coordination', 'XPO:0142051', 'abnormal cerebrospinal fluid', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(21827, 'HP:0007057', 'Poor hand-eye coordination', 'XPO:0100164', 'abnormal neural nucleus', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(21828, 'HP:0007057', 'Poor hand-eye coordination', 'XPO:0100427', 'abnormal olfactory system', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(21829, 'HP:0007057', 'Poor hand-eye coordination', 'XPO:0100031', 'abnormal central nervous system', 0.43333333333333335, 3.94131651835137, 1.3068679445984308, 'UPHENO:0004523', 'abnormal nervous system'),
(21830, 'HP:0007057', 'Poor hand-eye coordination', 'XPO:0100114', 'abnormal peripheral nervous system', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(21831, 'HP:0007057', 'Poor hand-eye coordination', 'XPO:0100273', 'abnormal visual system', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(21832, 'HP:0010907', 'Abnormal circulating proline concentration', 'XPO:0141905', 'abnormal ornithine metabolic process', 0.6029411764705882, 10.156767408123608, 2.474658216843727, 'UPHENO:0050249', 'abnormal alpha-amino acid metabolic process'),
(21833, 'HP:0010907', 'Abnormal circulating proline concentration', 'XPO:0141882', 'abnormal gamma-aminobutyric acid metabolic process', 0.5882352941176471, 10.007478699375595, 2.4262630063748842, 'UPHENO:0051195', 'abnormal amino acid metabolic process'),
(21834, 'HP:0010907', 'Abnormal circulating proline concentration', 'XPO:0141853', 'abnormal glutamate metabolic process', 0.6, 12.568193653850074, 2.746072867261545, 'UPHENO:0078648', 'abnormal glutamine family amino acid metabolic process'),
(21835, 'HP:0010907', 'Abnormal circulating proline concentration', 'XPO:0141922', 'abnormal valine metabolic process', 0.5942028985507246, 10.156767408123608, 2.456660463680844, 'UPHENO:0050249', 'abnormal alpha-amino acid metabolic process'),
(21836, 'HP:0010907', 'Abnormal circulating proline concentration', 'XPO:0141869', 'abnormal alpha-amino acid metabolic process', 0.6212121212121212, 10.156767408123608, 2.511873210625609, 'UPHENO:0050249', 'abnormal alpha-amino acid metabolic process'),
(21837, 'HP:0010907', 'Abnormal circulating proline concentration', 'XPO:0141843', 'abnormal alanine metabolic process', 0.6029411764705882, 10.156767408123608, 2.474658216843727, 'UPHENO:0050249', 'abnormal alpha-amino acid metabolic process'),
(21838, 'HP:0010907', 'Abnormal circulating proline concentration', 'XPO:0141913', 'abnormal L-serine metabolic process', 0.5857142857142857, 10.156767408123608, 2.4390497673510594, 'UPHENO:0050249', 'abnormal alpha-amino acid metabolic process'),
(21839, 'HP:0010907', 'Abnormal circulating proline concentration', 'XPO:0141896', 'abnormal lysine metabolic process', 0.5942028985507246, 10.156767408123608, 2.456660463680844, 'UPHENO:0050249', 'abnormal alpha-amino acid metabolic process'),
(21840, 'HP:0010907', 'Abnormal circulating proline concentration', 'XPO:0141893', 'abnormal isoleucine metabolic process', 0.5942028985507246, 10.156767408123608, 2.456660463680844, 'UPHENO:0050249', 'abnormal alpha-amino acid metabolic process'),
(21841, 'HP:0010907', 'Abnormal circulating proline concentration', 'XPO:0141848', 'abnormal proline metabolic process', 0.6417910447761194, 14.30515924801628, 3.0300038117918486, 'UPHENO:0078636', 'abnormal proline metabolic process'),
(21842, 'HP:0010907', 'Abnormal circulating proline concentration', 'XPO:0141857', 'abnormal glycine metabolic process', 0.5857142857142857, 10.156767408123608, 2.4390497673510594, 'UPHENO:0050249', 'abnormal alpha-amino acid metabolic process'),
(21843, 'HP:0010907', 'Abnormal circulating proline concentration', 'XPO:0141889', 'abnormal homoserine metabolic process', 0.5857142857142857, 10.156767408123608, 2.4390497673510594, 'UPHENO:0050249', 'abnormal alpha-amino acid metabolic process'),
(21844, 'HP:0010907', 'Abnormal circulating proline concentration', 'XPO:0141895', 'abnormal leucine metabolic process', 0.5942028985507246, 10.156767408123608, 2.456660463680844, 'UPHENO:0050249', 'abnormal alpha-amino acid metabolic process'),
(21845, 'HP:0010907', 'Abnormal circulating proline concentration', 'XPO:0141918', 'abnormal tyrosine metabolic process', 0.5942028985507246, 10.156767408123608, 2.456660463680844, 'UPHENO:0050249', 'abnormal alpha-amino acid metabolic process'),
(21846, 'HP:0010907', 'Abnormal circulating proline concentration', 'XPO:0141912', 'abnormal D-serine metabolic process', 0.5857142857142857, 10.156767408123608, 2.4390497673510594, 'UPHENO:0050249', 'abnormal alpha-amino acid metabolic process'),
(21847, 'HP:0010907', 'Abnormal circulating proline concentration', 'XPO:0141917', 'abnormal tryptophan metabolic process', 0.5942028985507246, 10.156767408123608, 2.456660463680844, 'UPHENO:0050249', 'abnormal alpha-amino acid metabolic process'),
(21848, 'HP:0010907', 'Abnormal circulating proline concentration', 'XPO:0141858', 'abnormal serine family amino acid metabolic process', 0.6029411764705882, 10.156767408123608, 2.474658216843727, 'UPHENO:0050249', 'abnormal alpha-amino acid metabolic process'),
(21849, 'HP:0010907', 'Abnormal circulating proline concentration', 'XPO:0141868', 'abnormal asparagine metabolic process', 0.5942028985507246, 10.156767408123608, 2.456660463680844, 'UPHENO:0050249', 'abnormal alpha-amino acid metabolic process'),
(21850, 'HP:0010907', 'Abnormal circulating proline concentration', 'XPO:0141847', 'abnormal arginine metabolic process', 0.6176470588235294, 12.568193653850074, 2.786163642901301, 'UPHENO:0078648', 'abnormal glutamine family amino acid metabolic process'),
(21851, 'HP:0010907', 'Abnormal circulating proline concentration', 'XPO:0141887', 'abnormal histidine metabolic process', 0.5942028985507246, 10.156767408123608, 2.456660463680844, 'UPHENO:0050249', 'abnormal alpha-amino acid metabolic process'),
(21852, 'HP:0010907', 'Abnormal circulating proline concentration', 'XPO:0141888', 'abnormal threonine metabolic process', 0.5942028985507246, 10.156767408123608, 2.456660463680844, 'UPHENO:0050249', 'abnormal alpha-amino acid metabolic process'),
(21853, 'HP:0010907', 'Abnormal circulating proline concentration', 'XPO:0141873', 'abnormal tricarboxylic acid metabolic process', 0.5147058823529411, 9.119292702704945, 2.1665072344629928, 'HP:0004354', 'Abnormal circulating carboxylic acid concentration'),
(21854, 'HP:0034119', 'Anti-GD1a IgG antibody positivity', 'XPO:0100745', 'abnormal anterior lymph sac', 0.40625, 5.64885357140806, 1.5148751642906173, 'HP:0002715', 'Abnormality of the immune system'),
(21855, 'HP:0034119', 'Anti-GD1a IgG antibody positivity', 'XPO:0101451', 'abnormal dorsal lymph space', 0.41935483870967744, 5.64885357140806, 1.5391147060347428, 'HP:0002715', 'Abnormality of the immune system'),
(21856, 'HP:0034119', 'Anti-GD1a IgG antibody positivity', 'XPO:0100232', 'abnormal lymphatic system', 0.4482758620689655, 5.64885357140806, 1.5913028324062968, 'HP:0002715', 'Abnormality of the immune system'),
(21857, 'HP:0034119', 'Anti-GD1a IgG antibody positivity', 'XPO:0100599', 'abnormal adult immune system', 0.43333333333333335, 5.64885357140806, 1.5645563421015427, 'HP:0002715', 'Abnormality of the immune system'),
(21858, 'HP:0034119', 'Anti-GD1a IgG antibody positivity', 'XPO:0101221', 'abnormal larval immune system', 0.43333333333333335, 5.64885357140806, 1.5645563421015427, 'HP:0002715', 'Abnormality of the immune system'),
(21859, 'HP:0034119', 'Anti-GD1a IgG antibody positivity', 'XPO:0100581', 'abnormal immune system', 0.4482758620689655, 5.64885357140806, 1.5913028324062968, 'HP:0002715', 'Abnormality of the immune system'),
(21860, 'HP:0001166', 'Arachnodactyly', 'XPO:0140219', 'abnormally necrotic forelimb digit', 0.4339622641509434, 7.492661022682715, 1.80320052737318, 'HP:0001167', 'Abnormal finger morphology'),
(21861, 'HP:0001166', 'Arachnodactyly', 'XPO:0128172', 'decreased size of the forelimb digit 3', 0.42342342342342343, 7.492661022682715, 1.781170452476563, 'HP:0001167', 'Abnormal finger morphology'),
(21862, 'HP:0001166', 'Arachnodactyly', 'XPO:0102787', 'abnormal forelimb digit 5 morphology', 0.46, 7.492661022682715, 1.8565085699866966, 'HP:0001167', 'Abnormal finger morphology'),
(21863, 'HP:0001166', 'Arachnodactyly', 'XPO:0101810', 'abnormal digit morphology', 0.40476190476190477, 6.466375519622663, 1.617820284280124, 'UPHENO:0086700', 'abnormal digit morphology'),
(21864, 'HP:0001166', 'Arachnodactyly', 'XPO:0129652', 'increased size of the forelimb digit 3', 0.4537037037037037, 7.492661022682715, 1.8437592187125542, 'HP:0001167', 'Abnormal finger morphology'),
(21865, 'HP:0001166', 'Arachnodactyly', 'XPO:0141108', 'abnormally necrotic forelimb digit 2', 0.42201834862385323, 7.492661022682715, 1.7782127070715896, 'HP:0001167', 'Abnormal finger morphology'),
(21866, 'HP:0001166', 'Arachnodactyly', 'XPO:0102529', 'abnormal forelimb digit 4 morphology', 0.46, 7.492661022682715, 1.8565085699866966, 'HP:0001167', 'Abnormal finger morphology'),
(21867, 'HP:0001166', 'Arachnodactyly', 'XPO:0103755', 'increased size of the forelimb digit', 0.4666666666666667, 7.492661022682715, 1.869913138067809, 'HP:0001167', 'Abnormal finger morphology'),
(21868, 'HP:0001166', 'Arachnodactyly', 'XPO:0130637', 'increased size of the forelimb digit 5', 0.4537037037037037, 7.492661022682715, 1.8437592187125542, 'HP:0001167', 'Abnormal finger morphology'),
(21869, 'HP:0001166', 'Arachnodactyly', 'XPO:0103465', 'bifurcated forelimb digit 2', 0.46846846846846846, 12.484129389061598, 2.4183508792265616, 'UPHENO:0041447', 'shape manual digit'),
(21870, 'HP:0001166', 'Arachnodactyly', 'XPO:0140898', 'abnormally necrotic forelimb digit 5', 0.42201834862385323, 7.492661022682715, 1.7782127070715896, 'HP:0001167', 'Abnormal finger morphology'),
(21871, 'HP:0001166', 'Arachnodactyly', 'XPO:0103467', 'bifurcated forelimb digit 4', 0.46846846846846846, 12.484129389061598, 2.4183508792265616, 'UPHENO:0041447', 'shape manual digit'),
(21872, 'HP:0001166', 'Arachnodactyly', 'XPO:0102746', 'abnormal forelimb digit 2 morphology', 0.46, 7.492661022682715, 1.8565085699866966, 'HP:0001167', 'Abnormal finger morphology'),
(21873, 'HP:0001166', 'Arachnodactyly', 'XPO:0129693', 'increased size of the digit', 0.4111111111111111, 6.466375519622663, 1.6304596973656729, 'UPHENO:0086700', 'abnormal digit morphology'),
(21874, 'HP:0001166', 'Arachnodactyly', 'XPO:0102880', 'abnormal digit-joint region morphology', 0.40476190476190477, 6.466375519622663, 1.617820284280124, 'UPHENO:0086700', 'abnormal digit morphology'),
(21875, 'HP:0001166', 'Arachnodactyly', 'XPO:0103432', 'decreased size of the forelimb digit', 0.4351851851851852, 7.492661022682715, 1.8057394813997938, 'HP:0001167', 'Abnormal finger morphology'),
(21876, 'HP:0001166', 'Arachnodactyly', 'XPO:0133358', 'fused forelimb digits', 0.42990654205607476, 7.492661022682715, 1.7947545768321247, 'HP:0001167', 'Abnormal finger morphology'),
(21877, 'HP:0001166', 'Arachnodactyly', 'XPO:0103779', 'decreased size of the forelimb digit in the regenerating forelimb', 0.40869565217391307, 7.492661022682715, 1.7499194219115835, 'HP:0001167', 'Abnormal finger morphology'),
(21878, 'HP:0001166', 'Arachnodactyly', 'XPO:0102214', 'abnormal forelimb digit morphology', 0.46938775510204084, 7.492661022682715, 1.8753568559550475, 'HP:0001167', 'Abnormal finger morphology'),
(21879, 'HP:0001166', 'Arachnodactyly', 'XPO:0141143', 'abnormally necrotic forelimb digit 3', 0.42201834862385323, 7.492661022682715, 1.7782127070715896, 'HP:0001167', 'Abnormal finger morphology'),
(21880, 'HP:0001166', 'Arachnodactyly', 'XPO:0103466', 'bifurcated forelimb digit 3', 0.46846846846846846, 12.484129389061598, 2.4183508792265616, 'UPHENO:0041447', 'shape manual digit'),
(21881, 'HP:0001166', 'Arachnodactyly', 'XPO:0103468', 'bifurcated forelimb digit 5', 0.46846846846846846, 12.484129389061598, 2.4183508792265616, 'UPHENO:0041447', 'shape manual digit'),
(21882, 'HP:0001166', 'Arachnodactyly', 'XPO:0129977', 'increased size of the digit-joint region', 0.42528735632183906, 6.466375519622663, 1.6583328223624414, 'UPHENO:0086700', 'abnormal digit morphology'),
(21883, 'HP:0001166', 'Arachnodactyly', 'XPO:0133378', 'fused forelimb digits part of regenerating forelimb', 0.40350877192982454, 7.492661022682715, 1.7387795857293602, 'HP:0001167', 'Abnormal finger morphology'),
(21884, 'HP:0001166', 'Arachnodactyly', 'XPO:0141556', 'abnormal forelimb digit morphology in the regenerating forelimb', 0.4423076923076923, 7.492661022682715, 1.820456427983539, 'HP:0001167', 'Abnormal finger morphology'),
(21885, 'HP:0001166', 'Arachnodactyly', 'XPO:0129161', 'decreased size of the forelimb digit 5', 0.42342342342342343, 7.492661022682715, 1.781170452476563, 'HP:0001167', 'Abnormal finger morphology'),
(21886, 'HP:0001166', 'Arachnodactyly', 'XPO:0130624', 'increased size of the forelimb digit 4', 0.4537037037037037, 7.492661022682715, 1.8437592187125542, 'HP:0001167', 'Abnormal finger morphology'),
(21887, 'HP:0001166', 'Arachnodactyly', 'XPO:0130664', 'increased size of the forelimb digit 2', 0.4537037037037037, 7.492661022682715, 1.8437592187125542, 'HP:0001167', 'Abnormal finger morphology'),
(21888, 'HP:0001166', 'Arachnodactyly', 'XPO:0102598', 'abnormal forelimb digit 3 morphology', 0.46, 7.492661022682715, 1.8565085699866966, 'HP:0001167', 'Abnormal finger morphology'),
(21889, 'HP:0001166', 'Arachnodactyly', 'XPO:0129188', 'decreased size of the forelimb digit 2', 0.42342342342342343, 7.492661022682715, 1.781170452476563, 'HP:0001167', 'Abnormal finger morphology'),
(21890, 'HP:0001166', 'Arachnodactyly', 'XPO:0129148', 'decreased size of the forelimb digit 4', 0.42342342342342343, 7.492661022682715, 1.781170452476563, 'HP:0001167', 'Abnormal finger morphology'),
(21891, 'HP:0001166', 'Arachnodactyly', 'XPO:0140716', 'abnormally necrotic forelimb digit 4', 0.42201834862385323, 7.492661022682715, 1.7782127070715896, 'HP:0001167', 'Abnormal finger morphology'),
(21892, 'HP:0008423', 'Spinal dysplasia', 'XPO:0102144', 'abnormal cranial skeleton morphology', 0.4666666666666667, 6.211345574613551, 1.702535736723214, 'UPHENO:0087089', 'abnormal axial skeleton plus cranial skeleton morphology'),
(21893, 'HP:0008423', 'Spinal dysplasia', 'XPO:0140043', 'abnormally necrotic perichondrium', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(21894, 'HP:0008423', 'Spinal dysplasia', 'XPO:0102761', 'abnormal cartilaginous condensation morphology', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(21895, 'HP:0008423', 'Spinal dysplasia', 'XPO:0128246', 'decreased size of the axial skeleton', 0.40384615384615385, 6.211345574613551, 1.5838017617482976, 'UPHENO:0087089', 'abnormal axial skeleton plus cranial skeleton morphology'),
(21896, 'HP:0008423', 'Spinal dysplasia', 'XPO:0101858', 'abnormal vertebral element morphology', 0.48148148148148145, 8.361863005979023, 2.006509952146755, 'UPHENO:0076695', 'abnormal vertebral column morphology'),
(21897, 'HP:0008423', 'Spinal dysplasia', 'XPO:0102567', 'abnormal skeleton morphology', 0.4878048780487805, 4.638757693672553, 1.5042634845863214, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(21898, 'HP:0008423', 'Spinal dysplasia', 'XPO:0101680', 'abnormal skeletal element morphology', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(21899, 'HP:0008423', 'Spinal dysplasia', 'XPO:0101740', 'abnormal cell part morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(21900, 'HP:0008423', 'Spinal dysplasia', 'XPO:0102217', 'abnormal elastica externa morphology', 0.5128205128205128, 4.638757693672553, 1.5423521320759594, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(21901, 'HP:0008423', 'Spinal dysplasia', 'XPO:0126886', 'abnormally localised vertebral column', 0.5, 8.05344015541032, 2.0066689008665977, 'UPHENO:0002813', 'abnormal vertebral column'),
(21902, 'HP:0008423', 'Spinal dysplasia', 'XPO:0102113', 'abnormal anatomical line morphology', 0.41935483870967744, 2.786899518863159, 1.0810641970914296, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(21903, 'HP:0008423', 'Spinal dysplasia', 'XPO:0130908', 'increased size of the notochordal sheath', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(21904, 'HP:0008423', 'Spinal dysplasia', 'XPO:0129434', 'decreased size of the notochordal sheath', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(21905, 'HP:0008423', 'Spinal dysplasia', 'XPO:0130368', 'increased size of the elastica externa', 0.43478260869565216, 4.638757693672553, 1.4201588541997616, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(21906, 'HP:0008423', 'Spinal dysplasia', 'XPO:0103737', 'increased size of the notochord', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(21907, 'HP:0008423', 'Spinal dysplasia', 'XPO:0141719', 'abnormal anterior notochord morphology', 0.4878048780487805, 4.638757693672553, 1.5042634845863214, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(21908, 'HP:0008423', 'Spinal dysplasia', 'XPO:0128306', 'decreased size of the articular system', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(21909, 'HP:0008423', 'Spinal dysplasia', 'XPO:0140350', 'abnormally necrotic notochordal sheath', 0.43478260869565216, 4.638757693672553, 1.4201588541997616, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(21910, 'HP:0008423', 'Spinal dysplasia', 'XPO:0102097', 'abnormal skeletal system morphology', 0.5128205128205128, 4.638757693672553, 1.5423521320759594, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(21911, 'HP:0008423', 'Spinal dysplasia', 'XPO:0103152', 'abnormal otic region morphology', 0.4107142857142857, 6.272837960958401, 1.6050994245019483, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(21912, 'HP:0008423', 'Spinal dysplasia', 'XPO:0128352', 'decreased size of the skeletal system', 0.43478260869565216, 4.638757693672553, 1.4201588541997616, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(21913, 'HP:0008423', 'Spinal dysplasia', 'XPO:0128158', 'decreased size of the skeletal subdivision', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(21914, 'HP:0008423', 'Spinal dysplasia', 'XPO:0102216', 'abnormal vertebral column morphology', 0.5652173913043478, 8.361863005979023, 2.1739987108284575, 'UPHENO:0076695', 'abnormal vertebral column morphology'),
(21915, 'HP:0008423', 'Spinal dysplasia', 'XPO:0139795', 'abnormally necrotic vertebral element', 0.41935483870967744, 8.361863005979023, 1.8725885058348382, 'UPHENO:0076695', 'abnormal vertebral column morphology'),
(21916, 'HP:0008423', 'Spinal dysplasia', 'XPO:0141713', 'increased size of the posterior notochord', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(21917, 'HP:0008423', 'Spinal dysplasia', 'XPO:0102325', 'abnormal vertebral centrum morphology', 0.4727272727272727, 8.361863005979023, 1.9881852765111048, 'UPHENO:0076695', 'abnormal vertebral column morphology'),
(21918, 'HP:0008423', 'Spinal dysplasia', 'XPO:0140510', 'abnormally necrotic postcranial axial skeleton', 0.45098039215686275, 6.272837960958401, 1.6819414150229712, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(21919, 'HP:0008423', 'Spinal dysplasia', 'XPO:0129664', 'increased size of the skeleton', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(21920, 'HP:0008423', 'Spinal dysplasia', 'XPO:0100226', 'abnormal vertebral element', 0.5319148936170213, 8.05344015541032, 2.0697209385605895, 'UPHENO:0002813', 'abnormal vertebral column'),
(21921, 'HP:0008423', 'Spinal dysplasia', 'XPO:0130188', 'increased size of the flexural organ', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(21922, 'HP:0008423', 'Spinal dysplasia', 'XPO:0102272', 'abnormal notochordal sheath morphology', 0.4878048780487805, 4.638757693672553, 1.5042634845863214, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(21923, 'HP:0008423', 'Spinal dysplasia', 'XPO:0141709', 'increased size of the anterior notochord', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(21924, 'HP:0008423', 'Spinal dysplasia', 'XPO:0102401', 'abnormal neurocranium morphology', 0.4107142857142857, 6.272837960958401, 1.6050994245019483, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(21925, 'HP:0008423', 'Spinal dysplasia', 'XPO:0101446', 'abnormal transverse process', 0.4166666666666667, 8.05344015541032, 1.8318297040812228, 'UPHENO:0002813', 'abnormal vertebral column'),
(21926, 'HP:0008423', 'Spinal dysplasia', 'XPO:0129707', 'increased size of the vertebral column', 0.48148148148148145, 8.361863005979023, 2.006509952146755, 'UPHENO:0076695', 'abnormal vertebral column morphology'),
(21927, 'HP:0008423', 'Spinal dysplasia', 'XPO:0140432', 'abnormally necrotic skeleton', 0.43478260869565216, 4.638757693672553, 1.4201588541997616, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(21928, 'HP:0008423', 'Spinal dysplasia', 'XPO:0128727', 'decreased size of the vertebral element', 0.40625, 8.361863005979023, 1.843097079965941, 'UPHENO:0076695', 'abnormal vertebral column morphology'),
(21929, 'HP:0008423', 'Spinal dysplasia', 'XPO:0141708', 'decreased size of the posterior notochord', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(21930, 'HP:0008423', 'Spinal dysplasia', 'XPO:0100584', 'abnormal vertebral column', 0.6097560975609756, 8.05344015541032, 2.2159950904963335, 'UPHENO:0002813', 'abnormal vertebral column'),
(21931, 'HP:0008423', 'Spinal dysplasia', 'XPO:0102605', 'abnormal dermal skeleton morphology', 0.45454545454545453, 4.638757693672553, 1.452076521536181, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(21932, 'HP:0008423', 'Spinal dysplasia', 'XPO:0100253', 'abnormal vertebra', 0.43103448275862066, 8.05344015541032, 1.863145300778979, 'UPHENO:0002813', 'abnormal vertebral column'),
(21933, 'HP:0008423', 'Spinal dysplasia', 'XPO:0127548', 'abnormally localised vertebral element', 0.43103448275862066, 8.05344015541032, 1.863145300778979, 'UPHENO:0002813', 'abnormal vertebral column'),
(21934, 'HP:0008423', 'Spinal dysplasia', 'XPO:0129726', 'increased size of the axial skeleton', 0.40384615384615385, 6.211345574613551, 1.5838017617482976, 'UPHENO:0087089', 'abnormal axial skeleton plus cranial skeleton morphology'),
(21935, 'HP:0008423', 'Spinal dysplasia', 'XPO:0140103', 'abnormally necrotic vertebral column', 0.5, 8.361863005979023, 2.0447326238385086, 'UPHENO:0076695', 'abnormal vertebral column morphology'),
(21936, 'HP:0008423', 'Spinal dysplasia', 'XPO:0130060', 'increased size of the postcranial axial skeleton', 0.4339622641509434, 6.272837960958401, 1.6499015013598524, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(21937, 'HP:0008423', 'Spinal dysplasia', 'XPO:0140683', 'abnormally necrotic flexural organ', 0.43478260869565216, 4.638757693672553, 1.4201588541997616, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(21938, 'HP:0008423', 'Spinal dysplasia', 'XPO:0141723', 'abnormal posterior notochord morphology', 0.4878048780487805, 4.638757693672553, 1.5042634845863214, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(21939, 'HP:0008423', 'Spinal dysplasia', 'XPO:0140019', 'abnormally necrotic skeletal system', 0.45454545454545453, 4.638757693672553, 1.452076521536181, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(21940, 'HP:0008423', 'Spinal dysplasia', 'XPO:0140852', 'abnormally necrotic vertebral centrum', 0.4126984126984127, 8.361863005979023, 1.8576672440911264, 'UPHENO:0076695', 'abnormal vertebral column morphology'),
(21941, 'HP:0008423', 'Spinal dysplasia', 'XPO:0102728', 'abnormal tendon morphology', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(21942, 'HP:0008423', 'Spinal dysplasia', 'XPO:0102093', 'abnormal craniofacial skeleton morphology', 0.44680851063829785, 6.211345574613551, 1.665917784661915, 'UPHENO:0087089', 'abnormal axial skeleton plus cranial skeleton morphology'),
(21943, 'HP:0008423', 'Spinal dysplasia', 'XPO:0141699', 'abnormally necrotic anterior notochord', 0.43478260869565216, 4.638757693672553, 1.4201588541997616, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(21944, 'HP:0008423', 'Spinal dysplasia', 'XPO:0100585', 'abnormal elastica externa', 0.4117647058823529, 4.3395673355180735, 1.3367425584480601, 'UPHENO:0002964', 'abnormal skeletal system'),
(21945, 'HP:0008423', 'Spinal dysplasia', 'XPO:0102542', 'abnormal vacuolated notochordal tissue morphology', 0.4444444444444444, 4.638757693672553, 1.4358516936218344, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(21946, 'HP:0008423', 'Spinal dysplasia', 'XPO:0102351', 'abnormal sphenoid region morphology', 0.4107142857142857, 6.272837960958401, 1.6050994245019483, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(21947, 'HP:0008423', 'Spinal dysplasia', 'XPO:0139917', 'abnormally necrotic notochord', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(21948, 'HP:0008423', 'Spinal dysplasia', 'XPO:0101860', 'abnormal skeletal subdivision morphology', 0.47619047619047616, 4.638757693672553, 1.4862477031377266, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(21949, 'HP:0008423', 'Spinal dysplasia', 'XPO:0141703', 'abnormally necrotic posterior notochord', 0.43478260869565216, 4.638757693672553, 1.4201588541997616, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(21950, 'HP:0008423', 'Spinal dysplasia', 'XPO:0102514', 'abnormal perichondrial cell morphology', 0.43478260869565216, 4.638757693672553, 1.4201588541997616, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(21951, 'HP:0008423', 'Spinal dysplasia', 'XPO:0129638', 'increased size of the skeletal subdivision', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(21952, 'HP:0008423', 'Spinal dysplasia', 'XPO:0129786', 'increased size of the articular system', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(21953, 'HP:0008423', 'Spinal dysplasia', 'XPO:0128184', 'decreased size of the skeleton', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(21954, 'HP:0008423', 'Spinal dysplasia', 'XPO:0130205', 'increased size of the vertebral element', 0.40625, 8.361863005979023, 1.843097079965941, 'UPHENO:0076695', 'abnormal vertebral column morphology'),
(21955, 'HP:0008423', 'Spinal dysplasia', 'XPO:0103116', 'abnormal bone marrow morphology', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(21956, 'HP:0008423', 'Spinal dysplasia', 'XPO:0128890', 'decreased size of the elastica externa', 0.43478260869565216, 4.638757693672553, 1.4201588541997616, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(21957, 'HP:0008423', 'Spinal dysplasia', 'XPO:0129832', 'increased size of the skeletal system', 0.43478260869565216, 4.638757693672553, 1.4201588541997616, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(21958, 'HP:0008423', 'Spinal dysplasia', 'XPO:0103218', 'abnormal joint morphology', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(21959, 'HP:0008423', 'Spinal dysplasia', 'XPO:0102828', 'abnormal occipital region morphology', 0.41818181818181815, 6.272837960958401, 1.6196255072310737, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(21960, 'HP:0008423', 'Spinal dysplasia', 'XPO:0100693', 'abnormal vertebral centrum', 0.5208333333333334, 8.05344015541032, 2.048047870764469, 'UPHENO:0002813', 'abnormal vertebral column'),
(21961, 'HP:0008423', 'Spinal dysplasia', 'XPO:0139774', 'abnormally necrotic elastica externa', 0.45454545454545453, 4.638757693672553, 1.452076521536181, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(21962, 'HP:0008423', 'Spinal dysplasia', 'XPO:0101713', 'abnormal anatomical entity in vitro morphology', 0.41935483870967744, 2.786899518863159, 1.0810641970914296, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(21963, 'HP:0008423', 'Spinal dysplasia', 'XPO:0102806', 'abnormal articular system morphology', 0.5, 4.638757693672553, 1.5229507040072823, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(21964, 'HP:0008423', 'Spinal dysplasia', 'XPO:0139889', 'abnormally necrotic cranial skeleton', 0.4117647058823529, 6.211345574613551, 1.599253852164941, 'UPHENO:0087089', 'abnormal axial skeleton plus cranial skeleton morphology'),
(21965, 'HP:0008423', 'Spinal dysplasia', 'XPO:0101957', 'abnormal axial skeleton morphology', 0.4772727272727273, 6.211345574613551, 1.7217740393063181, 'UPHENO:0087089', 'abnormal axial skeleton plus cranial skeleton morphology'),
(21966, 'HP:0008423', 'Spinal dysplasia', 'XPO:0125260', 'absent vertebral column', 0.4716981132075472, 8.05344015541032, 1.9490491338437168, 'UPHENO:0002813', 'abnormal vertebral column'),
(21967, 'HP:0008423', 'Spinal dysplasia', 'XPO:0102010', 'abnormal perichondrium morphology', 0.47619047619047616, 4.638757693672553, 1.4862477031377266, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(21968, 'HP:0008423', 'Spinal dysplasia', 'XPO:0128709', 'decreased size of the flexural organ', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(21969, 'HP:0008423', 'Spinal dysplasia', 'XPO:0107372', 'abnormal flexural organ morphology', 0.4878048780487805, 4.638757693672553, 1.5042634845863214, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(21970, 'HP:0008423', 'Spinal dysplasia', 'XPO:0100252', 'abnormal caudal vertebra', 0.4098360655737705, 8.05344015541032, 1.816752660002781, 'UPHENO:0002813', 'abnormal vertebral column'),
(21971, 'HP:0008423', 'Spinal dysplasia', 'XPO:0102461', 'abnormal postcranial axial skeleton morphology', 0.5111111111111111, 6.272837960958401, 1.7905633694581726, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(21972, 'HP:0008423', 'Spinal dysplasia', 'XPO:0102164', 'abnormal mandibular mesenchyme morphology', 0.42, 6.211345574613551, 1.61516721776344, 'UPHENO:0087089', 'abnormal axial skeleton plus cranial skeleton morphology'),
(21973, 'HP:0008423', 'Spinal dysplasia', 'XPO:0102980', 'abnormal perichordal tissue morphology', 0.4444444444444444, 4.638757693672553, 1.4358516936218344, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(21974, 'HP:0008423', 'Spinal dysplasia', 'XPO:0139771', 'abnormally necrotic skeletal subdivision', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(21975, 'HP:0008423', 'Spinal dysplasia', 'XPO:0128580', 'decreased size of the postcranial axial skeleton', 0.4339622641509434, 6.272837960958401, 1.6499015013598524, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(21976, 'HP:0008423', 'Spinal dysplasia', 'XPO:0140559', 'abnormally necrotic articular system', 0.4444444444444444, 4.638757693672553, 1.4358516936218344, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(21977, 'HP:0008423', 'Spinal dysplasia', 'XPO:0100927', 'abnormal sacral vertebra', 0.423728813559322, 8.05344015541032, 1.8472884566637167, 'UPHENO:0002813', 'abnormal vertebral column'),
(21978, 'HP:0008423', 'Spinal dysplasia', 'XPO:0125894', 'absent vertebral element', 0.4032258064516129, 8.05344015541032, 1.8020418700394085, 'UPHENO:0002813', 'abnormal vertebral column'),
(21979, 'HP:0008423', 'Spinal dysplasia', 'XPO:0101070', 'abnormal rib', 0.4166666666666667, 8.05344015541032, 1.8318297040812228, 'UPHENO:0002813', 'abnormal vertebral column'),
(21980, 'HP:0008423', 'Spinal dysplasia', 'XPO:0101976', 'abnormal portion of organism substance morphology', 0.41935483870967744, 2.786899518863159, 1.0810641970914296, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(21981, 'HP:0008423', 'Spinal dysplasia', 'XPO:0102130', 'abnormal endoskeleton morphology', 0.45454545454545453, 4.638757693672553, 1.452076521536181, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(21982, 'HP:0008423', 'Spinal dysplasia', 'XPO:0101982', 'abnormal appendicular skeleton morphology', 0.43478260869565216, 4.638757693672553, 1.4201588541997616, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(21983, 'HP:0008423', 'Spinal dysplasia', 'XPO:0126787', 'abnormally localised vertebral centrum', 0.423728813559322, 8.05344015541032, 1.8472884566637167, 'UPHENO:0002813', 'abnormal vertebral column'),
(21984, 'HP:0008423', 'Spinal dysplasia', 'XPO:0102054', 'abnormal notochord morphology', 0.4878048780487805, 4.638757693672553, 1.5042634845863214, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(21985, 'HP:0008423', 'Spinal dysplasia', 'XPO:0139998', 'abnormally necrotic axial skeleton', 0.42, 6.211345574613551, 1.61516721776344, 'UPHENO:0087089', 'abnormal axial skeleton plus cranial skeleton morphology'),
(21986, 'HP:0008423', 'Spinal dysplasia', 'XPO:0101638', 'abnormal anatomical structure morphology', 0.41935483870967744, 2.786899518863159, 1.0810641970914296, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(21987, 'HP:0008423', 'Spinal dysplasia', 'XPO:0100895', 'abnormal presacral vertebra', 0.423728813559322, 8.05344015541032, 1.8472884566637167, 'UPHENO:0002813', 'abnormal vertebral column'),
(21988, 'HP:0008423', 'Spinal dysplasia', 'XPO:0128227', 'decreased size of the vertebral column', 0.48148148148148145, 8.361863005979023, 2.006509952146755, 'UPHENO:0076695', 'abnormal vertebral column morphology'),
(21989, 'HP:0008423', 'Spinal dysplasia', 'XPO:0141704', 'decreased size of the anterior notochord', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(21990, 'HP:0008423', 'Spinal dysplasia', 'XPO:0102564', 'abnormal olfactory region morphology', 0.4107142857142857, 6.272837960958401, 1.6050994245019483, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(21991, 'HP:0008423', 'Spinal dysplasia', 'XPO:0101226', 'abnormal postsacral vertebra', 0.423728813559322, 8.05344015541032, 1.8472884566637167, 'UPHENO:0002813', 'abnormal vertebral column'),
(21992, 'HP:0033675', 'Frailty', 'XPO:0141743', 'abnormal chemical homeostasis within a tissue', 0.5714285714285714, 1.4755025719078136, 0.918228907628411, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(21993, 'HP:0033675', 'Frailty', 'XPO:0141783', 'abnormal collagen metabolic process', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(21994, 'HP:0033675', 'Frailty', 'XPO:0142052', 'abnormal nasal region', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(21995, 'HP:0033675', 'Frailty', 'XPO:0107273', 'abnormal basal region', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(21996, 'HP:0033675', 'Frailty', 'XPO:0100415', 'abnormal secretory epithelial cell', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(21997, 'HP:0033675', 'Frailty', 'XPO:0100307', 'abnormal blastomere', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(21998, 'HP:0033675', 'Frailty', 'XPO:0141880', 'abnormal ethanolamine metabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(21999, 'HP:0033675', 'Frailty', 'XPO:0100781', 'abnormal presumptive ectoderm', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22000, 'HP:0033675', 'Frailty', 'XPO:0131669', 'abnormal Roux spot', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(22001, 'HP:0033675', 'Frailty', 'XPO:0141792', 'abnormal small molecule metabolic process', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(22002, 'HP:0033675', 'Frailty', 'XPO:0131675', 'abnormal spindle microtubule', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(22003, 'HP:0033675', 'Frailty', 'XPO:0100025', 'abnormal oocyte', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(22004, 'HP:0033675', 'Frailty', 'XPO:0100186', 'abnormal uveal tract', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22005, 'HP:0033675', 'Frailty', 'XPO:0100501', 'abnormal urogenital system', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(22006, 'HP:0033675', 'Frailty', 'XPO:0101373', 'abnormal oxygen accumulating cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(22007, 'HP:0033675', 'Frailty', 'XPO:0141778', 'abnormal biosynthetic process', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(22008, 'HP:0033675', 'Frailty', 'XPO:0101040', 'abnormal axial mesoderm', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22009, 'HP:0033675', 'Frailty', 'XPO:0141760', 'abnormal multicellular organismal homeostasis', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22010, 'HP:0033675', 'Frailty', 'XPO:0131475', 'absent olfactory behavior', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22011, 'HP:0033675', 'Frailty', 'XPO:0141782', 'abnormal methylation', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(22012, 'HP:0033675', 'Frailty', 'XPO:0131481', 'absent feeding behavior', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22013, 'HP:0033675', 'Frailty', 'XPO:0101168', 'abnormal circulating cell', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(22014, 'HP:0033675', 'Frailty', 'XPO:0141907', 'abnormal putrescine metabolic process', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(22015, 'HP:0033675', 'Frailty', 'XPO:0100626', 'abnormal primordial germ cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(22016, 'HP:0033675', 'Frailty', 'XPO:0100721', 'abnormal centromere', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(22017, 'HP:0033675', 'Frailty', 'XPO:0100493', 'abnormal liver and biliary system', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(22018, 'HP:0033675', 'Frailty', 'XPO:0100282', 'abnormal pelvic girdle primordium', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22019, 'HP:0033675', 'Frailty', 'XPO:0141263', 'abnormal visually guided collision avoidance behavior', 0.5714285714285714, 1.4755025719078136, 0.918228907628411, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22020, 'HP:0033675', 'Frailty', 'XPO:0100704', 'abnormal Merkel cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(22021, 'HP:0033675', 'Frailty', 'XPO:0107278', 'abnormal medial region', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22022, 'HP:0033675', 'Frailty', 'XPO:0107271', 'abnormal apical region', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22023, 'HP:0033675', 'Frailty', 'XPO:0141748', 'abnormal gas homeostasis', 0.5714285714285714, 1.4755025719078136, 0.918228907628411, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22024, 'HP:0033675', 'Frailty', 'XPO:0101326', 'abnormal cementoblast', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(22025, 'HP:0033675', 'Frailty', 'XPO:0116429', 'abnormal behavior', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22026, 'HP:0033675', 'Frailty', 'XPO:0101311', 'abnormal bottle cell', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(22027, 'HP:0033675', 'Frailty', 'XPO:0101378', 'abnormal blastomere D1', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(22028, 'HP:0033675', 'Frailty', 'XPO:0100437', 'abnormal proepicardium', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(22029, 'HP:0033675', 'Frailty', 'XPO:0100547', 'abnormal blastomere V2', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(22030, 'HP:0033675', 'Frailty', 'XPO:0100784', 'abnormal left blastomere', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(22031, 'HP:0033675', 'Frailty', 'XPO:0100503', 'abnormal blastomere D2', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(22032, 'HP:0033675', 'Frailty', 'XPO:0142057', 'abnormal desmosome', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(22033, 'HP:0033675', 'Frailty', 'XPO:0107253', 'abnormal enteric nervous system', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(22034, 'HP:0033675', 'Frailty', 'XPO:0107268', 'abnormal left side', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22035, 'HP:0033675', 'Frailty', 'XPO:0141600', 'absent metamorphosis', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22036, 'HP:0033675', 'Frailty', 'XPO:0128000', 'absent behavior', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22037, 'HP:0033675', 'Frailty', 'XPO:0131728', 'abnormal regulation of cell size', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22038, 'HP:0033675', 'Frailty', 'XPO:0100912', 'abnormal trabecula', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22039, 'HP:0033675', 'Frailty', 'XPO:0141784', 'abnormal cellular hormone metabolic process', 0.5714285714285714, 1.4755025719078136, 0.918228907628411, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22040, 'HP:0033675', 'Frailty', 'XPO:0141718', 'abnormal posterior notochord', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(22041, 'HP:0033675', 'Frailty', 'XPO:0141814', 'abnormal lyase activity', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22042, 'HP:0033675', 'Frailty', 'XPO:0133402', 'absent determination of left/right symmetry in alimentary system', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22043, 'HP:0033675', 'Frailty', 'XPO:0100715', 'abnormal ciliated cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(22044, 'HP:0033675', 'Frailty', 'XPO:0131725', 'abnormal phosphorylation of RNA polymerase II C-terminal domain', 0.5714285714285714, 1.4755025719078136, 0.918228907628411, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22045, 'HP:0033675', 'Frailty', 'XPO:0101302', 'abnormal subcortical cytoplasm', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(22046, 'HP:0033675', 'Frailty', 'XPO:0101461', 'abnormal sperm entry point', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(22047, 'HP:0033675', 'Frailty', 'XPO:0100003', 'abnormal organism subdivision', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22048, 'HP:0033675', 'Frailty', 'XPO:0100545', 'abnormal male organism', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22049, 'HP:0033675', 'Frailty', 'XPO:0107258', 'abnormal anatomical axis', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22050, 'HP:0033675', 'Frailty', 'XPO:0131721', 'abnormal nodal signaling pathway', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22051, 'HP:0033675', 'Frailty', 'XPO:0142056', 'abnormal main body axis', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22052, 'HP:0033675', 'Frailty', 'XPO:0100852', 'abnormal interdigital region', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(22053, 'HP:0033675', 'Frailty', 'XPO:0141809', 'abnormal catalytic activity', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22054, 'HP:0033675', 'Frailty', 'XPO:0100268', 'abnormal circulatory system', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22055, 'HP:0033675', 'Frailty', 'XPO:0131474', 'absent behavioral response to pain', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22056, 'HP:0033675', 'Frailty', 'XPO:0100081', 'abnormal anatomical entity in vitro', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22057, 'HP:0033675', 'Frailty', 'XPO:0131722', 'abnormal determination of left/right symmetry', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22058, 'HP:0033675', 'Frailty', 'XPO:0103624', 'absent anterior/posterior pattern specification in midgut', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22059, 'HP:0033675', 'Frailty', 'XPO:0131667', 'abnormal actin cytoskeleton', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(22060, 'HP:0033675', 'Frailty', 'XPO:0100745', 'abnormal anterior lymph sac', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(22061, 'HP:0033675', 'Frailty', 'XPO:0100887', 'abnormal right-dorsal blastomere', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(22062, 'HP:0033675', 'Frailty', 'XPO:0101389', 'abnormal wedge region', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(22063, 'HP:0033675', 'Frailty', 'XPO:0131472', 'absent vocalization behavior', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22064, 'HP:0033675', 'Frailty', 'XPO:0141788', 'abnormal hormone biosynthetic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(22065, 'HP:0033675', 'Frailty', 'XPO:0100913', 'abnormal Brachets cleft', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22066, 'HP:0033675', 'Frailty', 'XPO:0101535', 'abnormal absorptive cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(22067, 'HP:0033675', 'Frailty', 'XPO:0107261', 'abnormal dorsal-ventral axis', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22068, 'HP:0033675', 'Frailty', 'XPO:0100344', 'abnormal portion of organism substance', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22069, 'HP:0033675', 'Frailty', 'XPO:0100265', 'abnormal sensory epithelial cell', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(22070, 'HP:0033675', 'Frailty', 'XPO:0141775', 'abnormal nitrogen compound metabolic process', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(22071, 'HP:0033675', 'Frailty', 'XPO:0100202', 'abnormal embryo', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22072, 'HP:0033675', 'Frailty', 'XPO:0100989', 'abnormal right blastomere', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(22073, 'HP:0033675', 'Frailty', 'XPO:0100023', 'abnormal mesenchyme', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22074, 'HP:0033675', 'Frailty', 'XPO:0131477', 'absent visual behavior', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22075, 'HP:0033675', 'Frailty', 'XPO:0141714', 'abnormal anterior notochord', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(22076, 'HP:0033675', 'Frailty', 'XPO:0100417', 'abnormal dense regular connective tissue', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(22077, 'HP:0033675', 'Frailty', 'XPO:0141968', 'absent cilium motility in ciliated cell', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22078, 'HP:0033675', 'Frailty', 'XPO:0141791', 'abnormal primary metabolic process', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(22079, 'HP:0033675', 'Frailty', 'XPO:0101569', 'abnormal activin-induced ectoderm', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22080, 'HP:0033675', 'Frailty', 'XPO:0107312', 'abnormal filopodium', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(22081, 'HP:0033675', 'Frailty', 'XPO:0107339', 'abnormal yolk platelet', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(22082, 'HP:0033675', 'Frailty', 'XPO:0100002', 'abnormal head', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(22083, 'HP:0033675', 'Frailty', 'XPO:0100791', 'abnormal multiciliated cell precursor', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(22084, 'HP:0033675', 'Frailty', 'XPO:0100640', 'abnormal notochordal sheath', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(22085, 'HP:0033675', 'Frailty', 'XPO:0100842', 'abnormal left-dorsal blastomere', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(22086, 'HP:0033675', 'Frailty', 'XPO:0101463', 'abnormal right-ventral blastomere', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(22087, 'HP:0033675', 'Frailty', 'XPO:0100728', 'abnormal cell condensation', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22088, 'HP:0033675', 'Frailty', 'XPO:0100422', 'abnormal notochord', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(22089, 'HP:0033675', 'Frailty', 'XPO:0115512', 'abnormally semi-erect whole organism', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22090, 'HP:0033675', 'Frailty', 'XPO:0100915', 'abnormal dermal system', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22091, 'HP:0033675', 'Frailty', 'XPO:0101074', 'abnormal germinal vesicle', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(22092, 'HP:0033675', 'Frailty', 'XPO:0101221', 'abnormal larval immune system', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(22093, 'HP:0033675', 'Frailty', 'XPO:0100277', 'abnormal blastocoel', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22094, 'HP:0033675', 'Frailty', 'XPO:0100585', 'abnormal elastica externa', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(22095, 'HP:0033675', 'Frailty', 'XPO:0100956', 'abnormal centrosome', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(22096, 'HP:0033675', 'Frailty', 'XPO:0100515', 'abnormal somatic stem cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(22097, 'HP:0033675', 'Frailty', 'XPO:0107288', 'abnormal larval alimentary system', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(22098, 'HP:0033675', 'Frailty', 'XPO:0131714', 'abnormal establishment of tissue polarity', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22099, 'HP:0033675', 'Frailty', 'XPO:0100120', 'abnormal genital system', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(22100, 'HP:0033675', 'Frailty', 'XPO:0100642', 'abnormal gustatory system', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(22101, 'HP:0033675', 'Frailty', 'XPO:0101497', 'abnormal ciliary axoneme', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(22102, 'HP:0033675', 'Frailty', 'XPO:0101071', 'abnormal endoplasmic reticulum', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(22103, 'HP:0033675', 'Frailty', 'XPO:0141499', 'abnormal tadpole', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22104, 'HP:0033675', 'Frailty', 'XPO:0115391', 'abnormally undifferentiated alimentary system', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(22105, 'HP:0033675', 'Frailty', 'XPO:0100999', 'abnormal serous membrane', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22106, 'HP:0033675', 'Frailty', 'XPO:0100031', 'abnormal central nervous system', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(22107, 'HP:0033675', 'Frailty', 'XPO:0141315', 'abnormal anatomical region', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22108, 'HP:0033675', 'Frailty', 'XPO:0100295', 'abnormal extracellular matrix', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22109, 'HP:0033675', 'Frailty', 'XPO:0100251', 'abnormal proteinaceous extracellular matrix', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22110, 'HP:0033675', 'Frailty', 'XPO:0141798', 'abnormal lipid metabolic process', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(22111, 'HP:0033675', 'Frailty', 'XPO:0100285', 'abnormal progenitor cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(22112, 'HP:0033675', 'Frailty', 'XPO:0100337', 'abnormal zygote', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(22113, 'HP:0033675', 'Frailty', 'XPO:0133388', 'absent insulin receptor signaling pathway', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22114, 'HP:0033675', 'Frailty', 'XPO:0131745', 'abnormal axis elongation', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(22115, 'HP:0033675', 'Frailty', 'XPO:0100674', 'abnormal secondary oogonium', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(22116, 'HP:0033675', 'Frailty', 'XPO:0107272', 'abnormal axial region', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22117, 'HP:0033675', 'Frailty', 'XPO:0100429', 'abnormal spermatid', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(22118, 'HP:0033675', 'Frailty', 'XPO:0131738', 'abnormal Wnt signaling pathway', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22119, 'HP:0033675', 'Frailty', 'XPO:0100802', 'abnormal exocrine cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(22120, 'HP:0033675', 'Frailty', 'XPO:0131666', 'abnormal adherens junction', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(22121, 'HP:0033675', 'Frailty', 'XPO:0100218', 'abnormal epithelial cell', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(22122, 'HP:0033675', 'Frailty', 'XPO:0100028', 'abnormal anatomical cluster', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22123, 'HP:0033675', 'Frailty', 'XPO:0100551', 'abnormal oocyte cortex', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(22124, 'HP:0033675', 'Frailty', 'XPO:0107265', 'abnormal posterior side', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22125, 'HP:0033675', 'Frailty', 'XPO:0100894', 'abnormal nucleus', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(22126, 'HP:0033675', 'Frailty', 'XPO:0100907', 'abnormal cytoplasm', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(22127, 'HP:0033675', 'Frailty', 'XPO:0100258', 'abnormal organ part', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22128, 'HP:0033675', 'Frailty', 'XPO:0141265', 'abnormal escape behavior', 0.5714285714285714, 1.4755025719078136, 0.918228907628411, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22129, 'HP:0033675', 'Frailty', 'XPO:0100232', 'abnormal lymphatic system', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(22130, 'HP:0033675', 'Frailty', 'XPO:0141772', 'abnormal water homeostasis', 0.5714285714285714, 1.4755025719078136, 0.918228907628411, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22131, 'HP:0033675', 'Frailty', 'XPO:0141962', 'absent cilium motility in pronephric kidney', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22132, 'HP:0033675', 'Frailty', 'XPO:0141810', 'abnormal cyclase activity', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22133, 'HP:0033675', 'Frailty', 'XPO:0100386', 'abnormal limb', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(22134, 'HP:0033675', 'Frailty', 'XPO:0101023', 'abnormal ultimobranchial body', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(22135, 'HP:0033675', 'Frailty', 'XPO:0100394', 'abnormal marginal zone', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22136, 'HP:0033675', 'Frailty', 'XPO:0100308', 'abnormal early embryonic cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(22137, 'HP:0033675', 'Frailty', 'XPO:0141264', 'abnormal schooling behavior', 0.5714285714285714, 1.4755025719078136, 0.918228907628411, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22138, 'HP:0033675', 'Frailty', 'XPO:0100192', 'abnormal epithelium', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22139, 'HP:0033675', 'Frailty', 'XPO:0101237', 'abnormal mucus secreting cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(22140, 'HP:0033675', 'Frailty', 'XPO:0100574', 'abnormal gastrula cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(22141, 'HP:0033675', 'Frailty', 'XPO:0100511', 'abnormal stylopod', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(22142, 'HP:0033675', 'Frailty', 'XPO:0100062', 'abnormal anatomical space', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22143, 'HP:0033675', 'Frailty', 'XPO:0131469', 'abnormal heart process', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22144, 'HP:0033675', 'Frailty', 'XPO:0141276', 'decreased surface breathing', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22145, 'HP:0033675', 'Frailty', 'XPO:0141790', 'abnormal cellular metabolic process', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(22146, 'HP:0033675', 'Frailty', 'XPO:0141871', 'abnormal cadaverine transport', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22147, 'HP:0033675', 'Frailty', 'XPO:0100423', 'abnormal process', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22148, 'HP:0033675', 'Frailty', 'XPO:0141795', 'abnormal glycosylation', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(22149, 'HP:0033675', 'Frailty', 'XPO:0141960', 'absent cilium motility in brain', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22150, 'HP:0033675', 'Frailty', 'XPO:0141815', 'abnormal isomerase activity', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22151, 'HP:0033675', 'Frailty', 'XPO:0133401', 'absent determination of left/right symmetry in lateral plate mesoderm', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22152, 'HP:0033675', 'Frailty', 'XPO:0131730', 'abnormal regulation of protein folding', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22153, 'HP:0033675', 'Frailty', 'XPO:0141272', 'absent surface breathing', 0.5714285714285714, 1.4755025719078136, 0.918228907628411, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22154, 'HP:0033675', 'Frailty', 'XPO:0131700', 'abnormal BMP signaling pathway', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22155, 'HP:0033675', 'Frailty', 'XPO:0100416', 'abnormal ligament', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(22156, 'HP:0033675', 'Frailty', 'XPO:0100599', 'abnormal adult immune system', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(22157, 'HP:0033675', 'Frailty', 'XPO:0133403', 'abnormal developmental process', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22158, 'HP:0033675', 'Frailty', 'XPO:0101176', 'abnormal non-ciliated epithelial cell', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(22159, 'HP:0033675', 'Frailty', 'XPO:0100976', 'abnormal multiciliated cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(22160, 'HP:0033675', 'Frailty', 'XPO:0100653', 'abnormal myoblast', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(22161, 'HP:0033675', 'Frailty', 'XPO:0100114', 'abnormal peripheral nervous system', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(22162, 'HP:0033675', 'Frailty', 'XPO:0141898', 'abnormal maltose metabolic process', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(22163, 'HP:0033675', 'Frailty', 'XPO:0100856', 'abnormal simple organ', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22164, 'HP:0033675', 'Frailty', 'XPO:0100688', 'abnormal adipose tissue', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(22165, 'HP:0033675', 'Frailty', 'XPO:0101467', 'abnormal alkali secreting cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(22166, 'HP:0033675', 'Frailty', 'XPO:0107284', 'abnormal migrating myoblast', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(22167, 'HP:0033675', 'Frailty', 'XPO:0100573', 'abnormal extraembryonic structure', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22168, 'HP:0033675', 'Frailty', 'XPO:0131798', 'abnormal development of anatomical space', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22169, 'HP:0033675', 'Frailty', 'XPO:0131480', 'absent mating behavior', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22170, 'HP:0033675', 'Frailty', 'XPO:0101264', 'abnormal mitotic spindle', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(22171, 'HP:0033675', 'Frailty', 'XPO:0100888', 'abnormal microtubule', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(22172, 'HP:0033675', 'Frailty', 'XPO:0101406', 'abnormal cleavage furrow', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22173, 'HP:0033675', 'Frailty', 'XPO:0101347', 'abnormal hindlimb region', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22174, 'HP:0033675', 'Frailty', 'XPO:0100557', 'abnormal prime meridian', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22175, 'HP:0033675', 'Frailty', 'XPO:0101109', 'abnormal egg cell-free extract', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22176, 'HP:0033675', 'Frailty', 'XPO:0141771', 'abnormal urea homeostasis', 0.5714285714285714, 1.4755025719078136, 0.918228907628411, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22177, 'HP:0033675', 'Frailty', 'XPO:0101498', 'abnormal stage II oocyte', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(22178, 'HP:0033675', 'Frailty', 'XPO:0131765', 'abnormal development of anatomical region', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22179, 'HP:0033675', 'Frailty', 'XPO:0131703', 'abnormal cell division', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22180, 'HP:0033675', 'Frailty', 'XPO:0141271', 'increased surface breathing', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22181, 'HP:0033675', 'Frailty', 'XPO:0101468', 'abnormal stage I oocyte', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(22182, 'HP:0033675', 'Frailty', 'XPO:0101228', 'abnormal mesenchymal stem cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(22183, 'HP:0033675', 'Frailty', 'XPO:0101448', 'abnormal myelin accumulating cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(22184, 'HP:0033675', 'Frailty', 'XPO:0141975', 'abnormal cilium motility', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22185, 'HP:0033675', 'Frailty', 'XPO:0100917', 'abnormal stage III oocyte', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(22186, 'HP:0033675', 'Frailty', 'XPO:0100069', 'abnormal urinary system', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(22187, 'HP:0033675', 'Frailty', 'XPO:0100643', 'abnormal thoracic region', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22188, 'HP:0033675', 'Frailty', 'XPO:0131719', 'abnormal activation of meiosis', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22189, 'HP:0033675', 'Frailty', 'XPO:0141715', 'abnormal septum', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22190, 'HP:0033675', 'Frailty', 'XPO:0100293', 'abnormal duct', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22191, 'HP:0033675', 'Frailty', 'XPO:0101519', 'abnormal hypobranchial placode', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22192, 'HP:0033675', 'Frailty', 'XPO:0141813', 'abnormal hydrolase activity', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22193, 'HP:0033675', 'Frailty', 'XPO:0101132', 'abnormal apoptotic cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(22194, 'HP:0033675', 'Frailty', 'XPO:0101362', 'abnormal vegetal cortex', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(22195, 'HP:0033675', 'Frailty', 'XPO:0131691', 'abnormal molecular function', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22196, 'HP:0033675', 'Frailty', 'XPO:0107285', 'abnormal flexural organ', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(22197, 'HP:0033675', 'Frailty', 'XPO:0101575', 'abnormal vitelline membrane', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(22198, 'HP:0033675', 'Frailty', 'XPO:0100006', 'abnormal anatomical structure', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22199, 'HP:0033675', 'Frailty', 'XPO:0100402', 'abnormal zeugopod', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(22200, 'HP:0033675', 'Frailty', 'XPO:0103783', 'absent hatching behavior', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22201, 'HP:0033675', 'Frailty', 'XPO:0101096', 'abnormal tendon', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(22202, 'HP:0033675', 'Frailty', 'XPO:0100010', 'abnormal multicellular anatomical structure', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22203, 'HP:0033675', 'Frailty', 'XPO:0141786', 'abnormal pigment metabolic process', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(22204, 'HP:0033675', 'Frailty', 'XPO:0131975', 'abnormal development of anatomical line', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22205, 'HP:0033675', 'Frailty', 'XPO:0131740', 'abnormal detection of nodal flow', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22206, 'HP:0033675', 'Frailty', 'XPO:0100610', 'abnormal appendage', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22207, 'HP:0033675', 'Frailty', 'XPO:0107264', 'abnormal anterior side', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22208, 'HP:0033675', 'Frailty', 'XPO:0115758', 'abnormally decreased mobility of melanoblast', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(22209, 'HP:0033675', 'Frailty', 'XPO:0133340', 'abnormal cell adhesion', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22210, 'HP:0033675', 'Frailty', 'XPO:0100862', 'abnormal blastomere V1', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(22211, 'HP:0033675', 'Frailty', 'XPO:0101570', 'abnormal forelimb region', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22212, 'HP:0033675', 'Frailty', 'XPO:0131482', 'absent locomotory behavior', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22213, 'HP:0033675', 'Frailty', 'XPO:0100991', 'abnormal iliac process primordium', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22214, 'HP:0033675', 'Frailty', 'XPO:0115508', 'abnormally peramorphic growth of whole organism', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22215, 'HP:0033675', 'Frailty', 'XPO:0131476', 'absent mechanosensory behavior', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22216, 'HP:0033675', 'Frailty', 'XPO:0100786', 'abnormal presumptive axial mesoderm', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22217, 'HP:0033675', 'Frailty', 'XPO:0101503', 'abnormal organ cortex', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22218, 'HP:0033675', 'Frailty', 'XPO:0100273', 'abnormal visual system', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(22219, 'HP:0033675', 'Frailty', 'XPO:0141776', 'abnormal metabolic process', 0.5555555555555556, 1.8210412618256888, 1.005827813247954, 'HP:0000118', 'Phenotypic abnormality'),
(22220, 'HP:0033675', 'Frailty', 'XPO:0100164', 'abnormal neural nucleus', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(22221, 'HP:0033675', 'Frailty', 'XPO:0100231', 'abnormal compound organ', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22222, 'HP:0033675', 'Frailty', 'XPO:0100458', 'abnormal autopod', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(22223, 'HP:0033675', 'Frailty', 'XPO:0100372', 'abnormal hematological system', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(22224, 'HP:0033675', 'Frailty', 'XPO:0141796', 'abnormal demethylation', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(22225, 'HP:0033675', 'Frailty', 'XPO:0142051', 'abnormal cerebrospinal fluid', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(22226, 'HP:0033675', 'Frailty', 'XPO:0141745', 'abnormal creatinine homeostasis', 0.5714285714285714, 1.4755025719078136, 0.918228907628411, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22227, 'HP:0033675', 'Frailty', 'XPO:0101472', 'abnormal zygote cortex', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(22228, 'HP:0033675', 'Frailty', 'XPO:0100060', 'abnormal regenerating tissue', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22229, 'HP:0033675', 'Frailty', 'XPO:0131711', 'abnormal establishment of cell polarity', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22230, 'HP:0033675', 'Frailty', 'XPO:0101136', 'abnormal ooplasm', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(22231, 'HP:0033675', 'Frailty', 'XPO:0101141', 'abnormal Keller explant', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22232, 'HP:0033675', 'Frailty', 'XPO:0100427', 'abnormal olfactory system', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(22233, 'HP:0033675', 'Frailty', 'XPO:0101283', 'abnormal left-ventral blastomere', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(22234, 'HP:0033675', 'Frailty', 'XPO:0141961', 'absent cilium motility in mucociliary epithelium', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22235, 'HP:0033675', 'Frailty', 'XPO:0100481', 'abnormal anatomical line', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22236, 'HP:0033675', 'Frailty', 'XPO:0100531', 'abnormal proliferative region', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22237, 'HP:0033675', 'Frailty', 'XPO:0141816', 'abnormal ligase activity', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22238, 'HP:0033675', 'Frailty', 'XPO:0131694', 'abnormal RNA polymerase II activity', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(22239, 'HP:0033675', 'Frailty', 'XPO:0100274', 'abnormal sensory system', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(22240, 'HP:0033675', 'Frailty', 'XPO:0141789', 'abnormal hormone catabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(22241, 'HP:0033675', 'Frailty', 'XPO:0100742', 'abnormal musculoskeletal system', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22242, 'HP:0033675', 'Frailty', 'XPO:0116433', 'abnormal axis specification', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22243, 'HP:0033675', 'Frailty', 'XPO:0131760', 'abnormal development of anatomical structure', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22244, 'HP:0033675', 'Frailty', 'XPO:0100384', 'abnormal amputated tissue', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22245, 'HP:0033675', 'Frailty', 'XPO:0141860', 'abnormal malate-aspartate shuttle', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(22246, 'HP:0033675', 'Frailty', 'XPO:0101174', 'abnormal articular system', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(22247, 'HP:0033675', 'Frailty', 'XPO:0131470', 'abnormal heart contraction', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22248, 'HP:0033675', 'Frailty', 'XPO:0101411', 'abnormal marginal zone (sensu neural)', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22249, 'HP:0033675', 'Frailty', 'XPO:0101240', 'abnormal ciliated non-epidermal cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(22250, 'HP:0033675', 'Frailty', 'XPO:0141781', 'abnormal secondary metabolic process', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(22251, 'HP:0033675', 'Frailty', 'XPO:0100549', 'abnormal mitotic cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(22252, 'HP:0033675', 'Frailty', 'XPO:0101451', 'abnormal dorsal lymph space', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(22253, 'HP:0033675', 'Frailty', 'XPO:0141266', 'abnormal surface breathing', 0.5714285714285714, 1.4755025719078136, 0.918228907628411, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22254, 'HP:0033675', 'Frailty', 'XPO:0100823', 'abnormal blood', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(22255, 'HP:0033675', 'Frailty', 'XPO:0141738', 'abnormal carbon dioxide homeostasis', 0.5714285714285714, 1.4755025719078136, 0.918228907628411, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22256, 'HP:0033675', 'Frailty', 'XPO:0100225', 'abnormal endocrine system', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(22257, 'HP:0033675', 'Frailty', 'XPO:0141965', 'absent cilium motility in alimentary system', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22258, 'HP:0033675', 'Frailty', 'XPO:0141892', 'abnormal inositol metabolic process', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(22259, 'HP:0033675', 'Frailty', 'XPO:0141744', 'abnormal chemical homeostasis', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22260, 'HP:0033675', 'Frailty', 'XPO:0100176', 'abnormal stage VI oocyte', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(22261, 'HP:0033675', 'Frailty', 'XPO:0116494', 'absent biological process', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22262, 'HP:0033675', 'Frailty', 'XPO:0100032', 'abnormal nervous system', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(22263, 'HP:0033675', 'Frailty', 'XPO:0115505', 'dead whole organism', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22264, 'HP:0033675', 'Frailty', 'XPO:0101110', 'abnormal cell-free extract', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22265, 'HP:0033675', 'Frailty', 'XPO:0141811', 'abnormal oxidoreductase activity', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22266, 'HP:0033675', 'Frailty', 'XPO:0100581', 'abnormal immune system', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(22267, 'HP:0033675', 'Frailty', 'XPO:0100762', 'abnormal intersomitic region', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22268, 'HP:0033675', 'Frailty', 'XPO:0100004', 'abnormal cell', 0.5263157894736842, 1.8210412618256888, 0.9790009036675816, 'HP:0000118', 'Phenotypic abnormality'),
(22269, 'HP:0033675', 'Frailty', 'XPO:0141812', 'abnormal transferase activity', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22270, 'HP:0033675', 'Frailty', 'XPO:0100289', 'abnormal chondroblast', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(22271, 'HP:0033675', 'Frailty', 'XPO:0107263', 'abnormal anatomical side', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22272, 'HP:0033675', 'Frailty', 'XPO:0141787', 'abnormal hormone metabolic process', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(22273, 'HP:0033675', 'Frailty', 'XPO:0100104', 'abnormal embryonic structure', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22274, 'HP:0033675', 'Frailty', 'XPO:0100151', 'abnormal primordium', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22275, 'HP:0033675', 'Frailty', 'XPO:0141963', 'absent cilium motility in pronephric nephrostome', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22276, 'HP:0033675', 'Frailty', 'XPO:0100108', 'abnormal cell part', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(22277, 'HP:0033675', 'Frailty', 'XPO:0101212', 'abnormal glomeral mesenchyme', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(22278, 'HP:0033675', 'Frailty', 'XPO:0116434', 'abnormal biological process', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22279, 'HP:0033675', 'Frailty', 'XPO:0107276', 'abnormal dorsal region', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22280, 'HP:0033675', 'Frailty', 'XPO:0100807', 'abnormal matrix-based tissue', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22281, 'HP:0033675', 'Frailty', 'XPO:0101333', 'abnormal barrier epithelial cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(22282, 'HP:0033675', 'Frailty', 'XPO:0101547', 'abnormal lampbrush chromosome', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(22283, 'HP:0033675', 'Frailty', 'XPO:0107266', 'abnormal dorsal side', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22284, 'HP:0033675', 'Frailty', 'XPO:0141767', 'abnormal temperature homeostasis', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(22285, 'HP:0033675', 'Frailty', 'XPO:0100162', 'abnormal presumptive rhombomere', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22286, 'HP:0033675', 'Frailty', 'XPO:0100465', 'abnormal skeletal system', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(22287, 'HP:0033675', 'Frailty', 'XPO:0100691', 'abnormal keratin accumulating cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(22288, 'HP:0033675', 'Frailty', 'XPO:0100239', 'abnormal acellular anatomical structure', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22289, 'HP:0033675', 'Frailty', 'XPO:0100026', 'abnormal germ cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(22290, 'HP:0033675', 'Frailty', 'XPO:0101366', 'abnormal morula cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(22291, 'HP:0033675', 'Frailty', 'XPO:0133397', 'abnormal insulin receptor signaling pathway', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22292, 'HP:0033675', 'Frailty', 'XPO:0100969', 'abnormal disaggregated/reaggregated ectoderm treated with activin', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22293, 'HP:0033675', 'Frailty', 'XPO:0131729', 'abnormal regulation of growth rate', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22294, 'HP:0033675', 'Frailty', 'XPO:0131685', 'abnormal cortical actin cytoskeleton', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(22295, 'HP:0033675', 'Frailty', 'XPO:0141841', 'abnormality of whole organism mass', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(22296, 'HP:0033675', 'Frailty', 'XPO:0100377', 'abnormal connective tissue', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(22297, 'HP:0033675', 'Frailty', 'XPO:0132054', 'abnormal development of portion of organism substance', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22298, 'HP:0033675', 'Frailty', 'XPO:0100205', 'abnormal limb segment', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(22299, 'HP:0033675', 'Frailty', 'XPO:0141818', 'abnormal peptidoglycan muralytic activity', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22300, 'HP:0033675', 'Frailty', 'XPO:0101513', 'abnormal basal body', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(22301, 'HP:0033675', 'Frailty', 'XPO:0141958', 'absent cilium motility in left-right organizer', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22302, 'HP:0033675', 'Frailty', 'XPO:0100665', 'abnormal egg jelly', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22303, 'HP:0033675', 'Frailty', 'XPO:0101113', 'abnormal stage IV oocyte', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(22304, 'HP:0033675', 'Frailty', 'XPO:0107270', 'abnormal proximal-distal axis', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22305, 'HP:0033675', 'Frailty', 'XPO:0107262', 'abnormal left-right axis', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22306, 'HP:0033675', 'Frailty', 'XPO:0100339', 'abnormal circumblastoporal collar', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22307, 'HP:0033675', 'Frailty', 'XPO:0107259', 'abnormal animal-vegetal axis', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22308, 'HP:0033675', 'Frailty', 'XPO:0100902', 'abnormal spermatocyte', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(22309, 'HP:0033675', 'Frailty', 'XPO:0101220', 'abnormal centriole', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(22310, 'HP:0033675', 'Frailty', 'XPO:0101004', 'abnormal acid secreting cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(22311, 'HP:0033675', 'Frailty', 'XPO:0100014', 'abnormal tissue', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22312, 'HP:0033675', 'Frailty', 'XPO:0107260', 'abnormal anterior-posterior axis', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22313, 'HP:0033675', 'Frailty', 'XPO:0141777', 'abnormal catabolic process', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(22314, 'HP:0033675', 'Frailty', 'XPO:0100084', 'abnormal anatomical group', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22315, 'HP:0033675', 'Frailty', 'XPO:0101241', 'abnormal nucleate erythrocyte', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(22316, 'HP:0033675', 'Frailty', 'XPO:0100392', 'abnormal cilium', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(22317, 'HP:0033675', 'Frailty', 'XPO:0101480', 'abnormal stage V oocyte', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(22318, 'HP:0033675', 'Frailty', 'XPO:0100899', 'abnormal secondary spermatogonium', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(22319, 'HP:0033675', 'Frailty', 'XPO:0101405', 'abnormal ring structure', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(22320, 'HP:0033675', 'Frailty', 'XPO:0101078', 'abnormal mucous gland', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22321, 'HP:0033675', 'Frailty', 'XPO:0100533', 'abnormal melanoblast', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(22322, 'HP:0033675', 'Frailty', 'XPO:0131479', 'absent social behavior', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22323, 'HP:0033675', 'Frailty', 'XPO:0141267', 'abnormal resting posture', 0.5714285714285714, 1.4755025719078136, 0.918228907628411, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22324, 'HP:0033675', 'Frailty', 'XPO:0131677', 'abnormal actin filament', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(22325, 'HP:0033675', 'Frailty', 'XPO:0100638', 'abnormal polar body', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(22326, 'HP:0033675', 'Frailty', 'XPO:0100152', 'abnormal alimentary system', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(22327, 'HP:0033675', 'Frailty', 'XPO:0141794', 'abnormal prosthetic group metabolic process', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(22328, 'HP:0033675', 'Frailty', 'XPO:0100477', 'abnormal pericyte', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(22329, 'HP:0033675', 'Frailty', 'XPO:0131723', 'abnormal pathway-restricted SMAD protein phosphorylation', 0.5714285714285714, 1.4755025719078136, 0.918228907628411, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22330, 'HP:0033675', 'Frailty', 'XPO:0101409', 'abnormal perivitelline space', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(22331, 'HP:0033675', 'Frailty', 'XPO:0141964', 'absent cilium motility in olfactory pit', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22332, 'HP:0033675', 'Frailty', 'XPO:0100587', 'abnormal vestibuloauditory system', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(22333, 'HP:0033675', 'Frailty', 'XPO:0141904', 'abnormal glucosamine metabolic process', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(22334, 'HP:0033675', 'Frailty', 'XPO:0100317', 'abnormal respiratory system', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(22335, 'HP:0033675', 'Frailty', 'XPO:0101157', 'abnormal female organism', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22336, 'HP:0033675', 'Frailty', 'XPO:0100754', 'abnormal electrically active cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(22337, 'HP:0033675', 'Frailty', 'XPO:0100724', 'abnormal kinetochore', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(22338, 'HP:0033675', 'Frailty', 'XPO:0107269', 'abnormal right side', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22339, 'HP:0033675', 'Frailty', 'XPO:0100900', 'abnormal angioblast', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(22340, 'HP:0033675', 'Frailty', 'XPO:0100135', 'abnormal surface structure', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22341, 'HP:0033675', 'Frailty', 'XPO:0141770', 'abnormal urate homeostasis', 0.5714285714285714, 1.4755025719078136, 0.918228907628411, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22342, 'HP:0033675', 'Frailty', 'XPO:0141724', 'abnormal prevention of polyspermy', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22343, 'HP:0033675', 'Frailty', 'XPO:0131715', 'abnormal fibroblast growth factor receptor signaling pathway', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22344, 'HP:0033675', 'Frailty', 'XPO:0101061', 'abnormal plasma membrane', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(22345, 'HP:0033675', 'Frailty', 'XPO:0100009', 'abnormal multi-tissue structure', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22346, 'HP:0033675', 'Frailty', 'XPO:00000000', 'Xenopus phenotype', 0.6153846153846154, 1.4755025719078136, 0.9528911704452407, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22347, 'HP:0033675', 'Frailty', 'XPO:0141959', 'absent cilium motility in floor plate', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22348, 'HP:0033675', 'Frailty', 'XPO:0107267', 'abnormal ventral side', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22349, 'HP:0033675', 'Frailty', 'XPO:0131705', 'abnormal chemotaxis', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22350, 'HP:0033675', 'Frailty', 'XPO:0131744', 'abnormal apical constriction', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22351, 'HP:0033675', 'Frailty', 'XPO:0101200', 'abnormal joint region', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22352, 'HP:0033675', 'Frailty', 'XPO:0141911', 'abnormal ribose phosphate metabolic process', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(22353, 'HP:0033675', 'Frailty', 'XPO:0141754', 'abnormal homeostatic process', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22354, 'HP:0033675', 'Frailty', 'XPO:0131687', 'abnormal astral microtubule', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(22355, 'HP:0033675', 'Frailty', 'XPO:0101072', 'abnormal mitochondrial cloud', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(22356, 'HP:0033675', 'Frailty', 'XPO:0100667', 'abnormal vegetal yolk mass', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22357, 'HP:0033675', 'Frailty', 'XPO:0141817', 'abnormal demethylase activity', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22358, 'HP:0033675', 'Frailty', 'XPO:0141797', 'abnormal hydrogen metabolic process', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(22359, 'HP:0033675', 'Frailty', 'XPO:0141877', 'abnormal 2-deoxyribose 1-phosphate metabolic process', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(22360, 'HP:0033675', 'Frailty', 'XPO:0100172', 'abnormal stem cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(22361, 'HP:0033675', 'Frailty', 'XPO:0100546', 'abnormal whole organism', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22362, 'HP:0033675', 'Frailty', 'XPO:0101435', 'abnormal paracrine cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(22363, 'HP:0033675', 'Frailty', 'XPO:0100363', 'abnormal cardiovascular system', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22364, 'HP:0033675', 'Frailty', 'XPO:0115509', 'abnormally semi-viable whole organism', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22365, 'HP:0033675', 'Frailty', 'XPO:0100070', 'abnormal anatomical system', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22366, 'HP:0033675', 'Frailty', 'XPO:0101297', 'abnormal barrier cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(22367, 'HP:0011611', 'Interrupted aortic arch', 'XPO:0103091', 'abnormal arteria iliaca communis morphology', 0.4090909090909091, 8.750570396338642, 1.8920303376273255, 'HP:0011004', 'Abnormal systemic arterial morphology'),
(22368, 'HP:0011611', 'Interrupted aortic arch', 'XPO:0103215', 'abnormal truncus arteriosus morphology', 0.46153846153846156, 6.974839882869777, 1.7942008998484034, 'UPHENO:0087186', 'abnormal blood vessel morphology'),
(22369, 'HP:0011611', 'Interrupted aortic arch', 'XPO:0101675', 'abnormal vein morphology', 0.45454545454545453, 7.803720102857406, 1.8833867105028699, 'HP:0033353', 'Abnormal blood vessel morphology'),
(22370, 'HP:0011611', 'Interrupted aortic arch', 'XPO:0128030', 'decreased size of the blood vessel', 0.42105263157894735, 6.974839882869777, 1.7137020416408788, 'UPHENO:0087186', 'abnormal blood vessel morphology'),
(22371, 'HP:0011611', 'Interrupted aortic arch', 'XPO:0103189', 'abnormal Jacobsons vein morphology', 0.43859649122807015, 7.803720102857406, 1.8500497981511776, 'HP:0033353', 'Abnormal blood vessel morphology'),
(22372, 'HP:0011611', 'Interrupted aortic arch', 'XPO:0102748', 'abnormal lateral vein morphology', 0.4032258064516129, 7.803720102857406, 1.7738831223610367, 'HP:0033353', 'Abnormal blood vessel morphology'),
(22373, 'HP:0011611', 'Interrupted aortic arch', 'XPO:0101712', 'abnormal aorta morphology', 0.543859649122807, 9.604719529875187, 2.2855238772414723, 'UPHENO:0076809', 'abnormal aorta morphology'),
(22374, 'HP:0011611', 'Interrupted aortic arch', 'XPO:0103217', 'abnormal dorsal longitudinal anastomosing vessel - right branch morphology', 0.4444444444444444, 6.974839882869777, 1.7606614770679263, 'UPHENO:0087186', 'abnormal blood vessel morphology'),
(22375, 'HP:0011611', 'Interrupted aortic arch', 'XPO:0102962', 'abnormal postcaval vein morphology', 0.4032258064516129, 7.803720102857406, 1.7738831223610367, 'HP:0033353', 'Abnormal blood vessel morphology'),
(22376, 'HP:0011611', 'Interrupted aortic arch', 'XPO:0102291', 'abnormal anterior cardinal vein morphology', 0.4032258064516129, 7.803720102857406, 1.7738831223610367, 'HP:0033353', 'Abnormal blood vessel morphology'),
(22377, 'HP:0011611', 'Interrupted aortic arch', 'XPO:0102412', 'abnormal vascular plexus morphology', 0.4528301886792453, 6.974839882869777, 1.7771938724200707, 'UPHENO:0087186', 'abnormal blood vessel morphology'),
(22378, 'HP:0011611', 'Interrupted aortic arch', 'XPO:0101829', 'abnormal subclavian vein morphology', 0.4032258064516129, 7.803720102857406, 1.7738831223610367, 'HP:0033353', 'Abnormal blood vessel morphology'),
(22379, 'HP:0011611', 'Interrupted aortic arch', 'XPO:0140809', 'abnormally necrotic truncus arteriosus', 0.41379310344827586, 6.974839882869777, 1.6988645152534954, 'UPHENO:0087186', 'abnormal blood vessel morphology'),
(22380, 'HP:0011611', 'Interrupted aortic arch', 'XPO:0102993', 'abnormal musculoabdominal vein morphology', 0.4032258064516129, 7.803720102857406, 1.7738831223610367, 'HP:0033353', 'Abnormal blood vessel morphology'),
(22381, 'HP:0011611', 'Interrupted aortic arch', 'XPO:0129573', 'increased size of the aorta', 0.4696969696969697, 9.604719529875187, 2.1239839118909725, 'UPHENO:0076809', 'abnormal aorta morphology'),
(22382, 'HP:0011611', 'Interrupted aortic arch', 'XPO:0102421', 'abnormal occipitovertebral artery morphology', 0.42857142857142855, 6.974839882869777, 1.7289352482549702, 'UPHENO:0087186', 'abnormal blood vessel morphology'),
(22383, 'HP:0011611', 'Interrupted aortic arch', 'XPO:0139803', 'abnormally necrotic aorta', 0.484375, 9.604719529875187, 2.156915858878898, 'UPHENO:0076809', 'abnormal aorta morphology'),
(22384, 'HP:0011611', 'Interrupted aortic arch', 'XPO:0101900', 'abnormal circulatory system morphology', 0.40425531914893614, 5.9590888072311134, 1.552093214856655, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(22385, 'HP:0011611', 'Interrupted aortic arch', 'XPO:0102284', 'abnormal medial cardinal vein morphology', 0.4032258064516129, 7.803720102857406, 1.7738831223610367, 'HP:0033353', 'Abnormal blood vessel morphology'),
(22386, 'HP:0011611', 'Interrupted aortic arch', 'XPO:0128364', 'decreased size of the dorsal aorta', 0.4189189189189189, 9.604719529875187, 2.0058910045101506, 'UPHENO:0076809', 'abnormal aorta morphology'),
(22387, 'HP:0011611', 'Interrupted aortic arch', 'XPO:0141134', 'abnormally necrotic caudal artery', 0.44285714285714284, 9.604719529875187, 2.0624060339672994, 'UPHENO:0076809', 'abnormal aorta morphology'),
(22388, 'HP:0011611', 'Interrupted aortic arch', 'XPO:0129184', 'decreased size of the arteria mesenterica posterior', 0.4246575342465753, 9.604719529875187, 2.0195832522297077, 'UPHENO:0076809', 'abnormal aorta morphology'),
(22389, 'HP:0011611', 'Interrupted aortic arch', 'XPO:0130660', 'increased size of the arteria mesenterica posterior', 0.4246575342465753, 9.604719529875187, 2.0195832522297077, 'UPHENO:0076809', 'abnormal aorta morphology'),
(22390, 'HP:0011611', 'Interrupted aortic arch', 'XPO:0102612', 'abnormal dorsal longitudinal anastomosing vessel - left branch morphology', 0.4444444444444444, 6.974839882869777, 1.7606614770679263, 'UPHENO:0087186', 'abnormal blood vessel morphology'),
(22391, 'HP:0011611', 'Interrupted aortic arch', 'XPO:0101708', 'abnormal artery morphology', 0.4444444444444444, 6.974839882869777, 1.7606614770679263, 'UPHENO:0087186', 'abnormal blood vessel morphology'),
(22392, 'HP:0011611', 'Interrupted aortic arch', 'XPO:0139730', 'abnormally necrotic vein', 0.4098360655737705, 7.803720102857406, 1.788364041182337, 'HP:0033353', 'Abnormal blood vessel morphology'),
(22393, 'HP:0011611', 'Interrupted aortic arch', 'XPO:0128147', 'decreased size of the ventral aorta', 0.4189189189189189, 9.604719529875187, 2.0058910045101506, 'UPHENO:0076809', 'abnormal aorta morphology'),
(22394, 'HP:0011611', 'Interrupted aortic arch', 'XPO:0101686', 'abnormal blood vessel morphology', 0.48, 6.974839882869777, 1.8297330799265483, 'UPHENO:0087186', 'abnormal blood vessel morphology'),
(22395, 'HP:0011611', 'Interrupted aortic arch', 'XPO:0102424', 'abnormal capillary morphology', 0.45454545454545453, 7.803720102857406, 1.8833867105028699, 'HP:0033353', 'Abnormal blood vessel morphology'),
(22396, 'HP:0011611', 'Interrupted aortic arch', 'XPO:0102619', 'abnormal larval aorta morphology', 0.42857142857142855, 6.974839882869777, 1.7289352482549702, 'UPHENO:0087186', 'abnormal blood vessel morphology'),
(22397, 'HP:0011611', 'Interrupted aortic arch', 'XPO:0140755', 'abnormally necrotic vascular plexus', 0.4067796610169492, 6.974839882869777, 1.6844058309093048, 'UPHENO:0087186', 'abnormal blood vessel morphology'),
(22398, 'HP:0011611', 'Interrupted aortic arch', 'XPO:0130819', 'increased size of the caudal artery', 0.4305555555555556, 9.604719529875187, 2.0335597736827666, 'UPHENO:0076809', 'abnormal aorta morphology'),
(22399, 'HP:0011611', 'Interrupted aortic arch', 'XPO:0140152', 'abnormally necrotic capillary', 0.4098360655737705, 7.803720102857406, 1.788364041182337, 'HP:0033353', 'Abnormal blood vessel morphology'),
(22400, 'HP:0011611', 'Interrupted aortic arch', 'XPO:0102166', 'abnormal medial abdominal vein morphology', 0.4032258064516129, 7.803720102857406, 1.7738831223610367, 'HP:0033353', 'Abnormal blood vessel morphology'),
(22401, 'HP:0011611', 'Interrupted aortic arch', 'XPO:0101780', 'abnormal arteria mesenterica posterior morphology', 0.484375, 9.604719529875187, 2.156915858878898, 'UPHENO:0076809', 'abnormal aorta morphology'),
(22402, 'HP:0011611', 'Interrupted aortic arch', 'XPO:0129510', 'increased size of the blood vessel', 0.42105263157894735, 6.974839882869777, 1.7137020416408788, 'UPHENO:0087186', 'abnormal blood vessel morphology'),
(22403, 'HP:0011611', 'Interrupted aortic arch', 'XPO:0101711', 'abnormal dorsal aorta morphology', 0.484375, 9.604719529875187, 2.156915858878898, 'UPHENO:0076809', 'abnormal aorta morphology'),
(22404, 'HP:0011611', 'Interrupted aortic arch', 'XPO:0139723', 'abnormally necrotic blood vessel', 0.43636363636363634, 6.974839882869777, 1.744582040015079, 'UPHENO:0087186', 'abnormal blood vessel morphology'),
(22405, 'HP:0011611', 'Interrupted aortic arch', 'XPO:0101774', 'abnormal paired dorsal aorta morphology', 0.5254237288135594, 9.604719529875187, 2.2464522139576966, 'UPHENO:0076809', 'abnormal aorta morphology'),
(22406, 'HP:0011611', 'Interrupted aortic arch', 'XPO:0101840', 'abnormal ventral aorta morphology', 0.484375, 9.604719529875187, 2.156915858878898, 'UPHENO:0076809', 'abnormal aorta morphology'),
(22407, 'HP:0011611', 'Interrupted aortic arch', 'XPO:0139828', 'abnormally necrotic paired dorsal aorta', 0.4626865671641791, 9.604719529875187, 2.1080736960203024, 'UPHENO:0076809', 'abnormal aorta morphology'),
(22408, 'HP:0011611', 'Interrupted aortic arch', 'XPO:0102904', 'abnormal lateral abdominal vein morphology', 0.4032258064516129, 7.803720102857406, 1.7738831223610367, 'HP:0033353', 'Abnormal blood vessel morphology'),
(22409, 'HP:0011611', 'Interrupted aortic arch', 'XPO:0129627', 'increased size of the ventral aorta', 0.4189189189189189, 9.604719529875187, 2.0058910045101506, 'UPHENO:0076809', 'abnormal aorta morphology'),
(22410, 'HP:0011611', 'Interrupted aortic arch', 'XPO:0101995', 'abnormal cardiovascular system morphology', 0.40425531914893614, 5.9590888072311134, 1.552093214856655, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(22411, 'HP:0011611', 'Interrupted aortic arch', 'XPO:0101916', 'abnormal tail vasculature morphology', 0.41379310344827586, 6.974839882869777, 1.6988645152534954, 'UPHENO:0087186', 'abnormal blood vessel morphology'),
(22412, 'HP:0011611', 'Interrupted aortic arch', 'XPO:0102355', 'abnormal lateral postcardinal vein morphology', 0.4032258064516129, 7.803720102857406, 1.7738831223610367, 'HP:0033353', 'Abnormal blood vessel morphology'),
(22413, 'HP:0011611', 'Interrupted aortic arch', 'XPO:0102709', 'abnormal ventral abdominal vein morphology', 0.4032258064516129, 7.803720102857406, 1.7738831223610367, 'HP:0033353', 'Abnormal blood vessel morphology'),
(22414, 'HP:0011611', 'Interrupted aortic arch', 'XPO:0101154', 'abnormal external carotid artery', 0.42857142857142855, 8.750570396338642, 1.9365547902328257, 'HP:0011004', 'Abnormal systemic arterial morphology'),
(22415, 'HP:0011611', 'Interrupted aortic arch', 'XPO:0101769', 'abnormal cardinal vein morphology', 0.423728813559322, 7.803720102857406, 1.818422684782831, 'HP:0033353', 'Abnormal blood vessel morphology'),
(22416, 'HP:0011611', 'Interrupted aortic arch', 'XPO:0128093', 'decreased size of the aorta', 0.4696969696969697, 9.604719529875187, 2.1239839118909725, 'UPHENO:0076809', 'abnormal aorta morphology'),
(22417, 'HP:0011611', 'Interrupted aortic arch', 'XPO:0129572', 'increased size of the paired dorsal aorta', 0.4492753623188406, 9.604719529875187, 2.0772972456428853, 'UPHENO:0076809', 'abnormal aorta morphology'),
(22418, 'HP:0011611', 'Interrupted aortic arch', 'XPO:0102251', 'abnormal interrenal vein morphology', 0.4032258064516129, 7.803720102857406, 1.7738831223610367, 'HP:0033353', 'Abnormal blood vessel morphology'),
(22419, 'HP:0011611', 'Interrupted aortic arch', 'XPO:0102683', 'abnormal intersomitic vein morphology', 0.41379310344827586, 6.974839882869777, 1.6988645152534954, 'UPHENO:0087186', 'abnormal blood vessel morphology'),
(22420, 'HP:0011611', 'Interrupted aortic arch', 'XPO:0141554', 'abnormal blood vessel morphology in the regenerating hindlimb', 0.42857142857142855, 6.974839882869777, 1.7289352482549702, 'UPHENO:0087186', 'abnormal blood vessel morphology'),
(22421, 'HP:0011611', 'Interrupted aortic arch', 'XPO:0140133', 'abnormally necrotic dorsal aorta', 0.4305555555555556, 9.604719529875187, 2.0335597736827666, 'UPHENO:0076809', 'abnormal aorta morphology'),
(22422, 'HP:0011611', 'Interrupted aortic arch', 'XPO:0102329', 'abnormal caudal artery morphology', 0.49206349206349204, 9.604719529875187, 2.1739668424704193, 'UPHENO:0076809', 'abnormal aorta morphology'),
(22423, 'HP:0011611', 'Interrupted aortic arch', 'XPO:0129844', 'increased size of the dorsal aorta', 0.4189189189189189, 9.604719529875187, 2.0058910045101506, 'UPHENO:0076809', 'abnormal aorta morphology'),
(22424, 'HP:0011611', 'Interrupted aortic arch', 'XPO:0140850', 'abnormally necrotic arteria mesenterica posterior', 0.43661971830985913, 9.604719529875187, 2.047830543667934, 'UPHENO:0076809', 'abnormal aorta morphology'),
(22425, 'HP:0011611', 'Interrupted aortic arch', 'XPO:0102565', 'abnormal branchial vein morphology', 0.43859649122807015, 7.803720102857406, 1.8500497981511776, 'HP:0033353', 'Abnormal blood vessel morphology'),
(22426, 'HP:0011611', 'Interrupted aortic arch', 'XPO:0102613', 'abnormal dorsal longitudinal anastomosing vessel morphology', 0.46153846153846156, 6.974839882869777, 1.7942008998484034, 'UPHENO:0087186', 'abnormal blood vessel morphology'),
(22427, 'HP:0011611', 'Interrupted aortic arch', 'XPO:0129344', 'decreased size of the caudal artery', 0.4305555555555556, 9.604719529875187, 2.0335597736827666, 'UPHENO:0076809', 'abnormal aorta morphology'),
(22428, 'HP:0011611', 'Interrupted aortic arch', 'XPO:0140595', 'abnormally necrotic dorsal longitudinal anastomosing vessel', 0.41379310344827586, 6.974839882869777, 1.6988645152534954, 'UPHENO:0087186', 'abnormal blood vessel morphology'),
(22429, 'HP:0011611', 'Interrupted aortic arch', 'XPO:0102875', 'abnormal vertebral artery morphology', 0.42857142857142855, 6.974839882869777, 1.7289352482549702, 'UPHENO:0087186', 'abnormal blood vessel morphology'),
(22430, 'HP:0011611', 'Interrupted aortic arch', 'XPO:0103063', 'abnormal ischiadic artery morphology', 0.42857142857142855, 6.974839882869777, 1.7289352482549702, 'UPHENO:0087186', 'abnormal blood vessel morphology'),
(22431, 'HP:0011611', 'Interrupted aortic arch', 'XPO:0128092', 'decreased size of the paired dorsal aorta', 0.4492753623188406, 9.604719529875187, 2.0772972456428853, 'UPHENO:0076809', 'abnormal aorta morphology'),
(22432, 'HP:0011611', 'Interrupted aortic arch', 'XPO:0101956', 'abnormal intersomitic vessel morphology', 0.42857142857142855, 6.974839882869777, 1.7289352482549702, 'UPHENO:0087186', 'abnormal blood vessel morphology'),
(22433, 'HP:0011611', 'Interrupted aortic arch', 'XPO:0102838', 'abnormal ischiadic vein morphology', 0.43859649122807015, 7.803720102857406, 1.8500497981511776, 'HP:0033353', 'Abnormal blood vessel morphology'),
(22434, 'HP:0011611', 'Interrupted aortic arch', 'XPO:0102154', 'abnormal subinterstitial vein morphology', 0.43859649122807015, 7.803720102857406, 1.8500497981511776, 'HP:0033353', 'Abnormal blood vessel morphology'),
(22435, 'HP:0011611', 'Interrupted aortic arch', 'XPO:0103212', 'abnormal cutaneous magnus morphology', 0.4032258064516129, 7.803720102857406, 1.7738831223610367, 'HP:0033353', 'Abnormal blood vessel morphology'),
(22436, 'HP:0011611', 'Interrupted aortic arch', 'XPO:0139802', 'abnormally necrotic ventral aorta', 0.4305555555555556, 9.604719529875187, 2.0335597736827666, 'UPHENO:0076809', 'abnormal aorta morphology'),
(22437, 'HP:0010608', 'Hordeolum internum', 'XPO:0129212', 'decreased size of the lower eyelid', 0.4024390243902439, 10.252047911556717, 2.031212485076075, 'HP:0000492', 'Abnormal eyelid morphology'),
(22438, 'HP:0010608', 'Hordeolum internum', 'XPO:0130688', 'increased size of the lower eyelid', 0.4024390243902439, 10.252047911556717, 2.031212485076075, 'HP:0000492', 'Abnormal eyelid morphology'),
(22439, 'HP:0010608', 'Hordeolum internum', 'XPO:0102723', 'abnormal lower eyelid morphology', 0.44594594594594594, 10.252047911556717, 2.1381906378530235, 'HP:0000492', 'Abnormal eyelid morphology'),
(22440, 'HP:0010608', 'Hordeolum internum', 'XPO:0140547', 'abnormally necrotic lower eyelid', 0.4125, 10.252047911556717, 2.056445905808647, 'HP:0000492', 'Abnormal eyelid morphology'),
(22441, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100842', 'abnormal left-dorsal blastomere', 0.52, 3.6715585125471644, 1.3817418089225373, 'UPHENO:0086172', 'abnormal cell'),
(22442, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100081', 'abnormal anatomical entity in vitro', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(22443, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0102347', 'abnormal ciliated cell morphology', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(22444, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0125750', 'absent melanoblast', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(22445, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100295', 'abnormal extracellular matrix', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(22446, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0101345', 'abnormal ascending interneuron', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(22447, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0127815', 'abnormally localised ciliated non-epidermal cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(22448, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0101467', 'abnormal alkali secreting cell', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(22449, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100203', 'abnormal endocrine cell', 0.48148148148148145, 3.6715585125471644, 1.3295816755533123, 'UPHENO:0086172', 'abnormal cell'),
(22450, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0101378', 'abnormal blastomere D1', 0.52, 3.6715585125471644, 1.3817418089225373, 'UPHENO:0086172', 'abnormal cell'),
(22451, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0125394', 'absent multiciliated cell precursor', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(22452, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100396', 'abnormal dorsal animal hemisphere blastomere', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(22453, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0141745', 'abnormal creatinine homeostasis', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22454, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0103041', 'abnormal perivitelline space morphology', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(22455, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100784', 'abnormal left blastomere', 0.52, 3.6715585125471644, 1.3817418089225373, 'UPHENO:0086172', 'abnormal cell'),
(22456, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0141263', 'abnormal visually guided collision avoidance behavior', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22457, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0131153', 'abnormally increased number of electrically active cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(22458, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:00000000', 'Xenopus phenotype', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22459, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0103005', 'abnormal oxygen accumulating cell morphology', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(22460, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100152', 'abnormal alimentary system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(22461, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0130979', 'abnormally increased number of Merkel cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(22462, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0101452', 'abnormal blastomere V1.1.1', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(22463, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100308', 'abnormal early embryonic cell', 0.5652173913043478, 3.6715585125471644, 1.440565418328227, 'UPHENO:0086172', 'abnormal cell'),
(22464, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0101109', 'abnormal egg cell-free extract', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(22465, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100574', 'abnormal gastrula cell', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(22466, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0127399', 'abnormally localised melanoblast', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(22467, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100372', 'abnormal hematological system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(22468, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100888', 'abnormal microtubule', 0.5652173913043478, 3.6715585125471644, 1.440565418328227, 'UPHENO:0086172', 'abnormal cell'),
(22469, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0141285', 'abnormal cortical actin cytoskeleton morphology', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(22470, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100477', 'abnormal pericyte', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(22471, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0101362', 'abnormal vegetal cortex', 0.5, 3.6715585125471644, 1.3549093166236559, 'UPHENO:0086172', 'abnormal cell'),
(22472, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0126737', 'abnormally localised mesenchymal stem cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(22473, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0125715', 'absent barrier cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(22474, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0131723', 'abnormal pathway-restricted SMAD protein phosphorylation', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22475, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0127018', 'abnormally localised ciliated cell', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(22476, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0107258', 'abnormal anatomical axis', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(22477, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0127339', 'abnormally localised migrating myoblast', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(22478, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100802', 'abnormal exocrine cell', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(22479, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0126738', 'abnormally localised paracrine cell', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(22480, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0131075', 'abnormally increased number of mucus secreting cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(22481, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0125061', 'absent basal body', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(22482, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100317', 'abnormal respiratory system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(22483, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0131090', 'abnormally increased number of oxygen accumulating cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(22484, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100872', 'abnormal neuroendocrine cell', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(22485, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0126473', 'abnormally localised germ cell', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(22486, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0101389', 'abnormal wedge region', 0.52, 3.6715585125471644, 1.3817418089225373, 'UPHENO:0086172', 'abnormal cell'),
(22487, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0126472', 'abnormally localised secondary spermatogonium', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(22488, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0141265', 'abnormal escape behavior', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22489, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0101358', 'abnormal endothelial cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(22490, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100031', 'abnormal central nervous system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(22491, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0131145', 'abnormally increased number of polar body', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(22492, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0101740', 'abnormal cell part morphology', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(22493, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0139717', 'abnormally necrotic cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(22494, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0102929', 'abnormal barrier cell morphology', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(22495, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0101228', 'abnormal mesenchymal stem cell', 0.5652173913043478, 3.6715585125471644, 1.440565418328227, 'UPHENO:0086172', 'abnormal cell'),
(22496, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0101466', 'abnormal secondary myofiber', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(22497, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100817', 'abnormal intersomitic neuron', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(22498, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0101494', 'abnormal blastomere D1.2.1', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(22499, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0101240', 'abnormal ciliated non-epidermal cell', 0.5652173913043478, 3.6715585125471644, 1.440565418328227, 'UPHENO:0086172', 'abnormal cell'),
(22500, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0131031', 'abnormally increased number of nucleate erythrocyte', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(22501, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0101113', 'abnormal stage IV oocyte', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(22502, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0101162', 'abnormal stromal cell', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(22503, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0101373', 'abnormal oxygen accumulating cell', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(22504, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0102183', 'abnormal oocyte cortex morphology', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(22505, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100969', 'abnormal disaggregated/reaggregated ectoderm treated with activin', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(22506, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0102285', 'abnormal myoblast morphology', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(22507, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100547', 'abnormal blastomere V2', 0.52, 3.6715585125471644, 1.3817418089225373, 'UPHENO:0086172', 'abnormal cell'),
(22508, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0142064', 'abnormal desmosome morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(22509, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100585', 'abnormal elastica externa', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(22510, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0125160', 'absent exocrine cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(22511, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0131061', 'abnormally increased number of keratin accumulating cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(22512, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0101405', 'abnormal ring structure', 0.52, 3.6715585125471644, 1.3817418089225373, 'UPHENO:0086172', 'abnormal cell'),
(22513, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100176', 'abnormal stage VI oocyte', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(22514, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100062', 'abnormal anatomical space', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(22515, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100415', 'abnormal secretory epithelial cell', 0.5, 3.6715585125471644, 1.3549093166236559, 'UPHENO:0086172', 'abnormal cell'),
(22516, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0125523', 'absent acid secreting cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(22517, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0131677', 'abnormal actin filament', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(22518, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0125743', 'absent lampbrush chromosome', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(22519, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100643', 'abnormal thoracic region', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(22520, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100691', 'abnormal keratin accumulating cell', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(22521, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0102896', 'abnormal mitotic spindle morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(22522, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0131129', 'abnormally increased number of chondroblast', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(22523, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100976', 'abnormal multiciliated cell', 0.5652173913043478, 3.6715585125471644, 1.440565418328227, 'UPHENO:0086172', 'abnormal cell'),
(22524, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0103037', 'abnormal ring structure morphology', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(22525, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0125530', 'absent chondroblast', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(22526, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100265', 'abnormal sensory epithelial cell', 0.5, 3.6715585125471644, 1.3549093166236559, 'UPHENO:0086172', 'abnormal cell'),
(22527, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100392', 'abnormal cilium', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(22528, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0125644', 'absent pericyte', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(22529, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0131551', 'abnormally localised actin cytoskeleton', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(22530, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100533', 'abnormal melanoblast', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(22531, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0127168', 'abnormally localised chondroblast', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(22532, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0102965', 'abnormal barrier epithelial cell morphology', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(22533, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100900', 'abnormal angioblast', 0.5, 3.6715585125471644, 1.3549093166236559, 'UPHENO:0086172', 'abnormal cell'),
(22534, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0131667', 'abnormal actin cytoskeleton', 0.5652173913043478, 3.6715585125471644, 1.440565418328227, 'UPHENO:0086172', 'abnormal cell'),
(22535, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100386', 'abnormal limb', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(22536, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0131550', 'abnormally localised adherens junction', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(22537, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0127160', 'abnormally localised acid secreting cell', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(22538, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0116091', 'abnormally increased variability of size of cell in endoderm', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(22539, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0102703', 'abnormal endoplasmic reticulum morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(22540, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0127337', 'abnormally localised oxygen accumulating cell', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(22541, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0126630', 'abnormally localised early embryonic cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(22542, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0131707', 'abnormal cilium assembly', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(22543, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0101198', 'abnormal digestive enzyme secreting cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(22544, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0101269', 'abnormal mesodermal cell', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(22545, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100675', 'abnormal dorsal vegetal hemisphere blastomere', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(22546, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100823', 'abnormal blood', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(22547, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100520', 'abnormal blastomere D1.2', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(22548, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100642', 'abnormal gustatory system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(22549, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0141315', 'abnormal anatomical region', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(22550, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100316', 'abnormal gamete', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(22551, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100014', 'abnormal tissue', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(22552, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0124984', 'absent progenitor cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(22553, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100728', 'abnormal cell condensation', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(22554, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0124934', 'absent centrosome', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(22555, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0126982', 'abnormally localised secondary oogonium', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(22556, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0127338', 'abnormally localised mucus secreting cell', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(22557, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0101264', 'abnormal mitotic spindle', 0.5652173913043478, 3.6715585125471644, 1.440565418328227, 'UPHENO:0086172', 'abnormal cell'),
(22558, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100218', 'abnormal epithelial cell', 0.52, 3.6715585125471644, 1.3817418089225373, 'UPHENO:0086172', 'abnormal cell'),
(22559, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0101221', 'abnormal larval immune system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(22560, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100852', 'abnormal interdigital region', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(22561, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100289', 'abnormal chondroblast', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(22562, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0101347', 'abnormal hindlimb region', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(22563, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0131165', 'abnormally increased number of cementoblast', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(22564, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100665', 'abnormal egg jelly', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(22565, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100175', 'abnormal migrating neuroblast', 0.48148148148148145, 3.6715585125471644, 1.3295816755533123, 'UPHENO:0086172', 'abnormal cell'),
(22566, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0101921', 'abnormal chondroblast morphology', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(22567, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0126697', 'abnormally localised proepicardium', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(22568, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100202', 'abnormal embryo', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(22569, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0127363', 'abnormally localised barrier cell', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(22570, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0131110', 'abnormally increased number of paracrine cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(22571, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0102109', 'abnormal pericyte morphology', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(22572, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0127631', 'abnormally localised centriole', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(22573, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0101016', 'abnormal egg', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(22574, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0141771', 'abnormal urea homeostasis', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22575, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100273', 'abnormal visual system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(22576, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0102873', 'abnormal nucleate erythrocyte morphology', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(22577, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0107339', 'abnormal yolk platelet', 0.52, 3.6715585125471644, 1.3817418089225373, 'UPHENO:0086172', 'abnormal cell'),
(22578, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0131512', 'absent adherens junction', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(22579, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0101110', 'abnormal cell-free extract', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(22580, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0131096', 'abnormally increased number of exocrine cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(22581, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0127435', 'abnormally localised mitotic spindle', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(22582, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0131066', 'abnormally increased number of myoblast', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(22583, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0103145', 'abnormal basal body morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(22584, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0107261', 'abnormal dorsal-ventral axis', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(22585, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100344', 'abnormal portion of organism substance', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(22586, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0101450', 'abnormal myeloid cell', 0.48148148148148145, 3.6715585125471644, 1.3295816755533123, 'UPHENO:0086172', 'abnormal cell'),
(22587, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0101326', 'abnormal cementoblast', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(22588, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0127653', 'abnormally localised Merkel cell', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(22589, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0124716', 'absent cell', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(22590, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0131136', 'abnormally increased number of multiciliated cell precursor', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(22591, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0101136', 'abnormal ooplasm', 0.52, 3.6715585125471644, 1.3817418089225373, 'UPHENO:0086172', 'abnormal cell'),
(22592, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0131513', 'absent actin cytoskeleton', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(22593, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100721', 'abnormal centromere', 0.5652173913043478, 3.6715585125471644, 1.440565418328227, 'UPHENO:0086172', 'abnormal cell'),
(22594, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100862', 'abnormal blastomere V1', 0.52, 3.6715585125471644, 1.3817418089225373, 'UPHENO:0086172', 'abnormal cell'),
(22595, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0101072', 'abnormal mitochondrial cloud', 0.52, 3.6715585125471644, 1.3817418089225373, 'UPHENO:0086172', 'abnormal cell'),
(22596, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0131706', 'abnormal ciliary basal body organization', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(22597, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0101448', 'abnormal myelin accumulating cell', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(22598, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0107286', 'abnormal efferent neuron', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(22599, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100967', 'abnormal blastomere V2.1.2', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(22600, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100481', 'abnormal anatomical line', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(22601, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0102704', 'abnormal mitochondrial cloud morphology', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(22602, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0126162', 'absent alkali secreting cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(22603, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100993', 'abnormal ligament cell', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(22604, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0102539', 'abnormal cytoplasm morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(22605, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100189', 'abnormal enteroendocrine cell', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(22606, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0130964', 'abnormally increased number of cell', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(22607, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0107278', 'abnormal medial region', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(22608, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0115508', 'abnormally peramorphic growth of whole organism', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(22609, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0101498', 'abnormal stage II oocyte', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(22610, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100754', 'abnormal electrically active cell', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(22611, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100070', 'abnormal anatomical system', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(22612, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0125824', 'absent nucleus', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(22613, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0101200', 'abnormal joint region', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(22614, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100573', 'abnormal extraembryonic structure', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(22615, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0130973', 'abnormally increased number of stem cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(22616, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0124845', 'absent stem cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(22617, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0101514', 'abnormal dendrite', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(22618, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0115509', 'abnormally semi-viable whole organism', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(22619, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100924', 'abnormal spermatozoon', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(22620, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100654', 'abnormal blastomere V2.1', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(22621, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0101237', 'abnormal mucus secreting cell', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(22622, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0107270', 'abnormal proximal-distal axis', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(22623, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0126214', 'absent microtubule', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(22624, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100702', 'abnormal glial cell', 0.48148148148148145, 3.6715585125471644, 1.3295816755533123, 'UPHENO:0086172', 'abnormal cell'),
(22625, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100009', 'abnormal multi-tissue structure', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(22626, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0127391', 'abnormally localised lampbrush chromosome', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(22627, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0127288', 'abnormally localised pericyte', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(22628, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0131654', 'abnormal neuron projection', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(22629, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100861', 'abnormal blastomere D2.2.2', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(22630, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100025', 'abnormal oocyte', 0.5652173913043478, 3.6715585125471644, 1.440565418328227, 'UPHENO:0086172', 'abnormal cell'),
(22631, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0101569', 'abnormal activin-induced ectoderm', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(22632, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0103642', 'increased cell population proliferation', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(22633, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0101022', 'abnormal blastomere V1.2', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(22634, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100882', 'abnormal perichondrial cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(22635, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0127806', 'abnormally localised spermatid', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(22636, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0101037', 'abnormal hatching gland cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(22637, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0107324', 'abnormal embryonic thrombocyte', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(22638, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100006', 'abnormal anatomical structure', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(22639, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0141498', 'abnormal axon microtubule bundle', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(22640, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0131708', 'abnormal cilium disassembly', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(22641, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0115512', 'abnormally semi-erect whole organism', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(22642, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100570', 'abnormal axon', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(22643, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0133441', 'abnormally increased number of cilium in the ciliated cell', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(22644, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0131675', 'abnormal spindle microtubule', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(22645, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0101500', 'abnormal endodermal cell', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(22646, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100239', 'abnormal acellular anatomical structure', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(22647, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0101374', 'abnormal migratory neural crest cell', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(22648, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100509', 'abnormal germ plasm', 0.48148148148148145, 3.6715585125471644, 1.3295816755533123, 'UPHENO:0086172', 'abnormal cell'),
(22649, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0103129', 'abnormal ciliary axoneme morphology', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(22650, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0126548', 'abnormally localised centrosome', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(22651, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100337', 'abnormal zygote', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(22652, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0127743', 'abnormally localised perivitelline space', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(22653, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0124864', 'absent germ cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(22654, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0130986', 'abnormally increased number of germ cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(22655, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0126159', 'absent apoptotic cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(22656, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0101576', 'abnormal blastomere V1.2.2', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(22657, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100437', 'abnormal proepicardium', 0.5652173913043478, 3.6715585125471644, 1.440565418328227, 'UPHENO:0086172', 'abnormal cell'),
(22658, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100546', 'abnormal whole organism', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(22659, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0141772', 'abnormal water homeostasis', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22660, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0131171', 'abnormally increased number of barrier epithelial cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(22661, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0101504', 'abnormal blastomere D2.2.1', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(22662, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100965', 'abnormal blastomere V2.2', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(22663, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0126133', 'absent mitotic cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(22664, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100859', 'abnormal blastomere V1.1.2', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(22665, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0102768', 'abnormal ooplasm morphology', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(22666, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0101570', 'abnormal forelimb region', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(22667, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0101535', 'abnormal absorptive cell', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(22668, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0125693', 'absent mucus secreting cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(22669, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100417', 'abnormal dense regular connective tissue', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(22670, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100732', 'abnormal tendon fibroblast', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(22671, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0102526', 'abnormal nucleus morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(22672, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100398', 'abnormal vegetal blastomere', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(22673, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0126681', 'abnormally localised basal body', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(22674, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0101350', 'abnormal blastomere D2.1.2', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(22675, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0107253', 'abnormal enteric nervous system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(22676, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0125384', 'absent ciliated cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(22677, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100688', 'abnormal adipose tissue', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(22678, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100397', 'abnormal ventral vegetal hemisphere blastomere', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(22679, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0102636', 'abnormal acid secreting cell morphology', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(22680, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0141296', 'abnormal adherens junction morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(22681, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0141784', 'abnormal cellular hormone metabolic process', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22682, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0103636', 'abnormally increased number of melanoblast', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(22683, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0102181', 'abnormal mitotic cell morphology', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(22684, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100551', 'abnormal oocyte cortex', 0.52, 3.6715585125471644, 1.3817418089225373, 'UPHENO:0086172', 'abnormal cell'),
(22685, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0107276', 'abnormal dorsal region', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(22686, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100336', 'abnormal interneuron', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(22687, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100004', 'abnormal cell', 0.6190476190476191, 3.6715585125471644, 1.5076039119696991, 'UPHENO:0086172', 'abnormal cell'),
(22688, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0131569', 'abnormally localised cortical actin cytoskeleton', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(22689, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0101132', 'abnormal apoptotic cell', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(22690, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100258', 'abnormal organ part', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(22691, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0141289', 'abnormal spindle microtubule morphology', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(22692, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0131134', 'abnormally increased number of barrier cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(22693, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0101468', 'abnormal stage I oocyte', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(22694, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0127343', 'abnormally localised filopodium', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(22695, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0101192', 'abnormal blastomere D2.1', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(22696, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0125785', 'absent mitotic spindle', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(22697, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0101168', 'abnormal circulating cell', 0.5, 3.6715585125471644, 1.3549093166236559, 'UPHENO:0086172', 'abnormal cell'),
(22698, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100674', 'abnormal secondary oogonium', 0.5652173913043478, 3.6715585125471644, 1.440565418328227, 'UPHENO:0086172', 'abnormal cell'),
(22699, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100449', 'abnormal lymphocyte', 0.48148148148148145, 3.6715585125471644, 1.3295816755533123, 'UPHENO:0086172', 'abnormal cell'),
(22700, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100649', 'abnormal growth cone', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(22701, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0127643', 'abnormally localised somatic stem cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(22702, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0126983', 'abnormally localised primordial germ cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(22703, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0101074', 'abnormal germinal vesicle', 0.5, 3.6715585125471644, 1.3549093166236559, 'UPHENO:0086172', 'abnormal cell'),
(22704, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0101220', 'abnormal centriole', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(22705, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0107260', 'abnormal anterior-posterior axis', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(22706, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0131685', 'abnormal cortical actin cytoskeleton', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(22707, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0101325', 'abnormal blastomere D2.1.1', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(22708, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100423', 'abnormal process', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(22709, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0142066', 'abnormally increased number of desmosome', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(22710, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0125053', 'absent zygote', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(22711, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0101061', 'abnormal plasma membrane', 0.5652173913043478, 3.6715585125471644, 1.440565418328227, 'UPHENO:0086172', 'abnormal cell'),
(22712, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100501', 'abnormal urogenital system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(22713, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0107263', 'abnormal anatomical side', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(22714, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0130989', 'abnormally increased number of ciliated cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(22715, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0107287', 'abnormal afferent neuron', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(22716, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0103104', 'abnormal zygote cortex morphology', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(22717, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0141314', 'abnormal Roux spot morphology', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(22718, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100429', 'abnormal spermatid', 0.5652173913043478, 3.6715585125471644, 1.440565418328227, 'UPHENO:0086172', 'abnormal cell'),
(22719, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0115505', 'dead whole organism', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(22720, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0101547', 'abnormal lampbrush chromosome', 0.5652173913043478, 3.6715585125471644, 1.440565418328227, 'UPHENO:0086172', 'abnormal cell'),
(22721, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0101239', 'abnormal olfactory epithelial support cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(22722, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0131082', 'abnormally increased number of alkali secreting cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(22723, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0125692', 'absent oxygen accumulating cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(22724, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0101157', 'abnormal female organism', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(22725, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100035', 'abnormal ventral animal hemisphere blastomere', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(22726, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0103167', 'abnormal absorptive cell morphology', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(22727, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100715', 'abnormal ciliated cell', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(22728, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0101534', 'abnormal blastomere V2.1.1', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(22729, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0125868', 'absent cementoblast', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(22730, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100599', 'abnormal adult immune system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(22731, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0102764', 'abnormal apoptotic cell morphology', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(22732, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0101463', 'abnormal right-ventral blastomere', 0.52, 3.6715585125471644, 1.3817418089225373, 'UPHENO:0086172', 'abnormal cell'),
(22733, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100864', 'abnormal dorsolateral ascending neuron', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(22734, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0101187', 'abnormal dorsolateral commissural neuron', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(22735, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0126413', 'abnormally localised cell part', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(22736, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0126388', 'abnormally localised oocyte', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(22737, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100277', 'abnormal blastocoel', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(22738, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0141497', 'abnormal lymphoblast', 0.48148148148148145, 3.6715585125471644, 1.3295816755533123, 'UPHENO:0086172', 'abnormal cell'),
(22739, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0141776', 'abnormal metabolic process', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(22740, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0102165', 'abnormal melanoblast morphology', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(22741, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100653', 'abnormal myoblast', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(22742, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0102588', 'abnormal centrosome morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(22743, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0142057', 'abnormal desmosome', 0.5652173913043478, 3.6715585125471644, 1.440565418328227, 'UPHENO:0086172', 'abnormal cell'),
(22744, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100713', 'abnormal monociliated cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(22745, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0127029', 'abnormally localised multiciliated cell precursor', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(22746, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100274', 'abnormal sensory system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(22747, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100084', 'abnormal anatomical group', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(22748, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0101917', 'abnormal progenitor cell morphology', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(22749, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0127821', 'abnormally localised apoptotic cell', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(22750, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0103093', 'abnormal sperm entry point morphology', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(22751, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100465', 'abnormal skeletal system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(22752, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0101141', 'abnormal Keller explant', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(22753, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0101133', 'abnormal motor neuron', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(22754, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0127979', 'abnormally localised absorptive cell', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(22755, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100108', 'abnormal cell part', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(22756, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0141272', 'absent surface breathing', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22757, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100954', 'abnormal neural progenitor cell', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(22758, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0127794', 'abnormally localised mitotic cell', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(22759, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0101083', 'abnormal T cell', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(22760, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0102336', 'abnormal Merkel cell morphology', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(22761, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100395', 'abnormal blastomere D1.1', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(22762, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100626', 'abnormal primordial germ cell', 0.5652173913043478, 3.6715585125471644, 1.440565418328227, 'UPHENO:0086172', 'abnormal cell'),
(22763, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0127876', 'abnormally localised microtubule', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(22764, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0124884', 'absent keratin accumulating cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(22765, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100596', 'abnormal myocyte', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(22766, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0142023', 'absent desmosome', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(22767, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0107323', 'abnormal thrombocyte', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(22768, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0101004', 'abnormal acid secreting cell', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(22769, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0102323', 'abnormal keratin accumulating cell morphology', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(22770, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0107272', 'abnormal axial region', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(22771, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0127217', 'abnormally localised cilium', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(22772, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0125533', 'absent myelin accumulating cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(22773, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0107271', 'abnormal apical region', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(22774, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0101079', 'abnormal blastomere D1.1.2', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(22775, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0126314', 'absent absorptive cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(22776, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0126783', 'abnormally localised exocrine cell', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(22777, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0127372', 'abnormally localised polar body', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(22778, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100569', 'abnormal motor axon', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(22779, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0125559', 'absent electrically active cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(22780, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0142065', 'abnormally decreased number of desmosome', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(22781, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0101366', 'abnormal morula cell', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(22782, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0102869', 'abnormal mucus secreting cell morphology', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(22783, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0102852', 'abnormal centriole morphology', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(22784, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100907', 'abnormal cytoplasm', 0.5652173913043478, 3.6715585125471644, 1.440565418328227, 'UPHENO:0086172', 'abnormal cell'),
(22785, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0101327', 'abnormal blastomere V1.2.1', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(22786, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0102024', 'abnormal cilium morphology', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(22787, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100724', 'abnormal kinetochore', 0.5652173913043478, 3.6715585125471644, 1.440565418328227, 'UPHENO:0086172', 'abnormal cell'),
(22788, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0103631', 'abnormally increased number of apoptotic cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(22789, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0101302', 'abnormal subcortical cytoplasm', 0.52, 3.6715585125471644, 1.3817418089225373, 'UPHENO:0086172', 'abnormal cell'),
(22790, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0101107', 'abnormal erythroid cell', 0.48148148148148145, 3.6715585125471644, 1.3295816755533123, 'UPHENO:0086172', 'abnormal cell'),
(22791, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0125997', 'absent Merkel cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(22792, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0131089', 'abnormally increased number of mitotic cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(22793, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0107426', 'abnormal yolk platelet morphology', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(22794, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100989', 'abnormal right blastomere', 0.52, 3.6715585125471644, 1.3817418089225373, 'UPHENO:0086172', 'abnormal cell'),
(22795, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0131180', 'abnormally decreased number of cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(22796, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0127824', 'abnormally localised alkali secreting cell', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(22797, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0126495', 'abnormally localised keratin accumulating cell', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(22798, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100843', 'abnormal fasciculated network of fibrils', 0.48148148148148145, 3.6715585125471644, 1.3295816755533123, 'UPHENO:0086172', 'abnormal cell'),
(22799, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0101497', 'abnormal ciliary axoneme', 0.52, 3.6715585125471644, 1.3817418089225373, 'UPHENO:0086172', 'abnormal cell'),
(22800, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0101241', 'abnormal nucleate erythrocyte', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(22801, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0127683', 'abnormally localised centromere', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(22802, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0103099', 'abnormal alkali secreting cell morphology', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(22803, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100172', 'abnormal stem cell', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(22804, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0126318', 'abnormally localised cell', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(22805, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100422', 'abnormal notochord', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(22806, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100960', 'abnormal postmigratory neural crest cell', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(22807, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0101480', 'abnormal stage V oocyte', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(22808, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100104', 'abnormal embryonic structure', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(22809, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0126454', 'abnormally localised stem cell', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(22810, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0131687', 'abnormal astral microtubule', 0.52, 3.6715585125471644, 1.3817418089225373, 'UPHENO:0086172', 'abnormal cell'),
(22811, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0127364', 'abnormally localised multiciliated cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(22812, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0101451', 'abnormal dorsal lymph space', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(22813, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0101587', 'abnormal hemangioblast', 0.48148148148148145, 3.6715585125471644, 1.3295816755533123, 'UPHENO:0086172', 'abnormal cell'),
(22814, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100026', 'abnormal germ cell', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(22815, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100335', 'abnormal commissural interneuron', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(22816, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0141743', 'abnormal chemical homeostasis within a tissue', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22817, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0101009', 'abnormal blastomere D1.1.1', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(22818, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0103080', 'abnormal myelin accumulating cell morphology', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(22819, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0101333', 'abnormal barrier epithelial cell', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(22820, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0102353', 'abnormal centromere morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(22821, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0127089', 'abnormally localised myoblast', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(22822, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0107311', 'abnormal apical junction complex', 0.48148148148148145, 3.6715585125471644, 1.3295816755533123, 'UPHENO:0086172', 'abnormal cell'),
(22823, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100894', 'abnormal nucleus', 0.5652173913043478, 3.6715585125471644, 1.440565418328227, 'UPHENO:0086172', 'abnormal cell'),
(22824, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0131669', 'abnormal Roux spot', 0.52, 3.6715585125471644, 1.3817418089225373, 'UPHENO:0086172', 'abnormal cell'),
(22825, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0127533', 'abnormally localised spermatocyte', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(22826, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0102934', 'abnormal subcortical cytoplasm morphology', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(22827, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100704', 'abnormal Merkel cell', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(22828, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0101283', 'abnormal left-ventral blastomere', 0.52, 3.6715585125471644, 1.3817418089225373, 'UPHENO:0086172', 'abnormal cell'),
(22829, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0103179', 'abnormal lampbrush chromosome morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(22830, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0127196', 'abnormally localised electrically active cell', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(22831, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100515', 'abnormal somatic stem cell', 0.5652173913043478, 3.6715585125471644, 1.440565418328227, 'UPHENO:0086172', 'abnormal cell'),
(22832, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0107312', 'abnormal filopodium', 0.5652173913043478, 3.6715585125471644, 1.440565418328227, 'UPHENO:0086172', 'abnormal cell'),
(22833, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100503', 'abnormal blastomere D2', 0.52, 3.6715585125471644, 1.3817418089225373, 'UPHENO:0086172', 'abnormal cell'),
(22834, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0101166', 'abnormal premigratory neural crest cell', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(22835, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0101658', 'abnormal germ cell morphology', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(22836, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0101485', 'abnormal descending interneuron', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(22837, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100762', 'abnormal intersomitic region', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(22838, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0101969', 'abnormal zygote morphology', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(22839, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100285', 'abnormal progenitor cell', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(22840, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0142030', 'abnormally localised desmosome', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(22841, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0124807', 'absent cell part', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(22842, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100901', 'abnormal blastomere D1.2.2', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(22843, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0102386', 'abnormal electrically active cell morphology', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(22844, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100887', 'abnormal right-dorsal blastomere', 0.52, 3.6715585125471644, 1.3817418089225373, 'UPHENO:0086172', 'abnormal cell'),
(22845, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100545', 'abnormal male organism', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(22846, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0126671', 'abnormally localised zygote', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(22847, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0107273', 'abnormal basal region', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(22848, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100917', 'abnormal stage III oocyte', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(22849, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0101518', 'abnormal B cell', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(22850, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0101636', 'abnormal cell morphology', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(22851, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0141299', 'abnormal actin filament morphology', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(22852, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0107262', 'abnormal left-right axis', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(22853, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0101461', 'abnormal sperm entry point', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(22854, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0131735', 'abnormal spindle assembly', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(22855, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100377', 'abnormal connective tissue', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(22856, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0101176', 'abnormal non-ciliated epithelial cell', 0.5, 3.6715585125471644, 1.3549093166236559, 'UPHENO:0086172', 'abnormal cell'),
(22857, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100587', 'abnormal vestibuloauditory system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(22858, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0125833', 'absent kinetochore', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(22859, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0103021', 'abnormal wedge region morphology', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(22860, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0141748', 'abnormal gas homeostasis', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22861, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0102356', 'abnormal kinetochore morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(22862, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0103067', 'abnormal paracrine cell morphology', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(22863, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0101575', 'abnormal vitelline membrane', 0.52, 3.6715585125471644, 1.3817418089225373, 'UPHENO:0086172', 'abnormal cell'),
(22864, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100814', 'abnormal natural killer cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(22865, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100307', 'abnormal blastomere', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(22866, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0133443', 'abnormally increased number of cilium in the multiciliated cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(22867, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0127522', 'abnormally localised cementoblast', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(22868, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0125859', 'absent nucleate erythrocyte', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(22869, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0127486', 'abnormally localised kinetochore', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(22870, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0141267', 'abnormal resting posture', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22871, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100427', 'abnormal olfactory system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(22872, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0101409', 'abnormal perivitelline space', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(22873, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0115758', 'abnormally decreased mobility of melanoblast', 0.5, 3.6715585125471644, 1.3549093166236559, 'UPHENO:0086172', 'abnormal cell'),
(22874, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0101411', 'abnormal marginal zone (sensu neural)', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(22875, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0102434', 'abnormal exocrine cell morphology', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(22876, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100232', 'abnormal lymphatic system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(22877, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100332', 'abnormal germinal granule', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(22878, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0101071', 'abnormal endoplasmic reticulum', 0.5652173913043478, 3.6715585125471644, 1.440565418328227, 'UPHENO:0086172', 'abnormal cell'),
(22879, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0125454', 'absent myoblast', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(22880, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100956', 'abnormal centrosome', 0.5652173913043478, 3.6715585125471644, 1.440565418328227, 'UPHENO:0086172', 'abnormal cell'),
(22881, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100902', 'abnormal spermatocyte', 0.5652173913043478, 3.6715585125471644, 1.440565418328227, 'UPHENO:0086172', 'abnormal cell'),
(22882, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0103894', 'abnormally decreased number of spindle microtubule', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(22883, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100521', 'abnormal animal blastomere', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(22884, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0141499', 'abnormal tadpole', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(22885, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0131032', 'abnormally increased number of acid secreting cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(22886, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100899', 'abnormal secondary spermatogonium', 0.5652173913043478, 3.6715585125471644, 1.440565418328227, 'UPHENO:0086172', 'abnormal cell'),
(22887, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0102693', 'abnormal plasma membrane morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(22888, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0133471', 'abnormally decreased number of cilium in the ciliated cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(22889, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100205', 'abnormal limb segment', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(22890, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100676', 'abnormal blastomere D2.2', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(22891, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0102520', 'abnormal microtubule morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(22892, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0141738', 'abnormal carbon dioxide homeostasis', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22893, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0133445', 'abnormally increased number of cilium in the ciliated non-epidermal cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(22894, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0141266', 'abnormal surface breathing', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22895, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0141277', 'abnormal actin cytoskeleton morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(22896, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0125698', 'absent filopodium', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(22897, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0131666', 'abnormal adherens junction', 0.5652173913043478, 3.6715585125471644, 1.440565418328227, 'UPHENO:0086172', 'abnormal cell'),
(22898, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0101158', 'abnormal blastomere V2.2.2', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(22899, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0102958', 'abnormal cementoblast morphology', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(22900, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100225', 'abnormal endocrine system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(22901, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0125779', 'absent endoplasmic reticulum', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(22902, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0127513', 'abnormally localised nucleate erythrocyte', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(22903, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0130988', 'abnormally increased number of pericyte', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(22904, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0131561', 'abnormally localised actin filament', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(22905, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100581', 'abnormal immune system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(22906, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100549', 'abnormal mitotic cell', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(22907, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0101435', 'abnormal paracrine cell', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(22908, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100733', 'abnormal fibroblast', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(22909, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0127171', 'abnormally localised myelin accumulating cell', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(22910, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0101490', 'abnormal ectodermal cell', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(22911, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0125854', 'absent barrier epithelial cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(22912, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100791', 'abnormal multiciliated cell precursor', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(22913, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0126600', 'abnormally localised progenitor cell', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(22914, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0125115', 'absent paracrine cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(22915, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0141770', 'abnormal urate homeostasis', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22916, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0131725', 'abnormal phosphorylation of RNA polymerase II C-terminal domain', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22917, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0107325', 'abnormal adult thrombocyte', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(22918, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0101311', 'abnormal bottle cell', 0.52, 3.6715585125471644, 1.3817418089225373, 'UPHENO:0086172', 'abnormal cell'),
(22919, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100701', 'abnormal microglial cell', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(22920, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100196', 'abnormal neuron', 0.48148148148148145, 3.6715585125471644, 1.3295816755533123, 'UPHENO:0086172', 'abnormal cell'),
(22921, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100638', 'abnormal polar body', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(22922, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0102423', 'abnormal multiciliated cell precursor morphology', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(22923, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0107284', 'abnormal migrating myoblast', 0.5652173913043478, 3.6715585125471644, 1.440565418328227, 'UPHENO:0086172', 'abnormal cell'),
(22924, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0101094', 'abnormal blastomere V2.2.1', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(22925, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100010', 'abnormal multicellular anatomical structure', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(22926, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0131131', 'abnormally increased number of absorptive cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(22927, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100003', 'abnormal organism subdivision', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(22928, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0127476', 'abnormally localised nucleus', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(22929, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0101472', 'abnormal zygote cortex', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(22930, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0131130', 'abnormally increased number of myelin accumulating cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(22931, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0107259', 'abnormal animal-vegetal axis', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(22932, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100028', 'abnormal anatomical cluster', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(22933, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0141264', 'abnormal schooling behavior', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22934, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0127428', 'abnormally localised endoplasmic reticulum', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(22935, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0101513', 'abnormal basal body', 0.5652173913043478, 3.6715585125471644, 1.440565418328227, 'UPHENO:0086172', 'abnormal cell'),
(22936, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0127508', 'abnormally localised barrier epithelial cell', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(22937, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0107399', 'abnormal filopodium morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(22938, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0101297', 'abnormal barrier cell', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(22939, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100032', 'abnormal nervous system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(22940, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0100034', 'abnormal blastomere V1.1', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(22941, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0101804', 'abnormal stem cell morphology', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(22942, 'HP:0031559', 'Reduced fibroblast CD16 level', 'XPO:0101120', 'abnormal cardiac progenitor cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(22943, 'HP:0012817', 'Noncompaction cardiomyopathy', 'XPO:0101900', 'abnormal circulatory system morphology', 0.40476190476190477, 5.9590888072311134, 1.5530653998657664, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(22944, 'HP:0012817', 'Noncompaction cardiomyopathy', 'XPO:0101995', 'abnormal cardiovascular system morphology', 0.40476190476190477, 5.9590888072311134, 1.5530653998657664, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(22945, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0100967', 'abnormal blastomere V2.1.2', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(22946, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0101079', 'abnormal blastomere D1.1.2', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(22947, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0101072', 'abnormal mitochondrial cloud', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(22948, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0100888', 'abnormal microtubule', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(22949, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0102353', 'abnormal centromere morphology', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(22950, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0100643', 'abnormal thoracic region', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(22951, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0127508', 'abnormally localised barrier epithelial cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(22952, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0107261', 'abnormal dorsal-ventral axis', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(22953, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0127653', 'abnormally localised Merkel cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(22954, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0101107', 'abnormal erythroid cell', 0.5, 3.6715585125471644, 1.3549093166236559, 'UPHENO:0086172', 'abnormal cell'),
(22955, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0141877', 'abnormal 2-deoxyribose 1-phosphate metabolic process', 0.4230769230769231, 4.758907843651163, 1.418937661667548, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(22956, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0142065', 'abnormally decreased number of desmosome', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(22957, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0107271', 'abnormal apical region', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(22958, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0101535', 'abnormal absorptive cell', 0.6190476190476191, 3.6715585125471644, 1.5076039119696991, 'UPHENO:0086172', 'abnormal cell'),
(22959, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0107263', 'abnormal anatomical side', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(22960, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0126783', 'abnormally localised exocrine cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(22961, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0100377', 'abnormal connective tissue', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(22962, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0131685', 'abnormal cortical actin cytoskeleton', 0.5652173913043478, 3.6715585125471644, 1.440565418328227, 'UPHENO:0086172', 'abnormal cell'),
(22963, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0102860', 'abnormal mesenchymal stem cell morphology', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(22964, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0100691', 'abnormal keratin accumulating cell', 0.6190476190476191, 3.6715585125471644, 1.5076039119696991, 'UPHENO:0086172', 'abnormal cell'),
(22965, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0102994', 'abnormal vegetal cortex morphology', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(22966, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0107339', 'abnormal yolk platelet', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(22967, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0126413', 'abnormally localised cell part', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(22968, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0126982', 'abnormally localised secondary oogonium', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(22969, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0131292', 'abnormally decreased number of mucus secreting cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(22970, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0100754', 'abnormal electrically active cell', 0.6190476190476191, 3.6715585125471644, 1.5076039119696991, 'UPHENO:0086172', 'abnormal cell'),
(22971, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0125577', 'absent cilium', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(22972, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0127824', 'abnormally localised alkali secreting cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(22973, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0139293', 'decreased cell population proliferation in organ part', 0.42857142857142855, 5.835653092541957, 1.5814531869511603, 'HP:0011017', 'Abnormal cellular physiology'),
(22974, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0127806', 'abnormally localised spermatid', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(22975, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0100704', 'abnormal Merkel cell', 0.6190476190476191, 3.6715585125471644, 1.5076039119696991, 'UPHENO:0086172', 'abnormal cell'),
(22976, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0131082', 'abnormally increased number of alkali secreting cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(22977, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0139625', 'decreased cell population proliferation in antero-dorsal region', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(22978, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0102061', 'abnormal spermatid morphology', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(22979, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0125698', 'absent filopodium', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(22980, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0138818', 'decreased cell population proliferation in portion of organism substance', 0.4411764705882353, 5.835653092541957, 1.6045413160604438, 'HP:0011017', 'Abnormal cellular physiology'),
(22981, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0127743', 'abnormally localised perivitelline space', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(22982, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0127979', 'abnormally localised absorptive cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(22983, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0131090', 'abnormally increased number of oxygen accumulating cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(22984, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0131723', 'abnormal pathway-restricted SMAD protein phosphorylation', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(22985, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0125394', 'absent multiciliated cell precursor', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(22986, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0136568', 'increased cell population proliferation in dorso-lateral region', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(22987, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0101158', 'abnormal blastomere V2.2.2', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(22988, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0127486', 'abnormally localised kinetochore', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(22989, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0107265', 'abnormal posterior side', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(22990, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0100965', 'abnormal blastomere V2.2', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(22991, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0103005', 'abnormal oxygen accumulating cell morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(22992, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0101237', 'abnormal mucus secreting cell', 0.6190476190476191, 3.6715585125471644, 1.5076039119696991, 'UPHENO:0086172', 'abnormal cell'),
(22993, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0100626', 'abnormal primordial germ cell', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(22994, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0141788', 'abnormal hormone biosynthetic process', 0.4074074074074074, 4.758907843651163, 1.392413123563799, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(22995, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0127876', 'abnormally localised microtubule', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(22996, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0100023', 'abnormal mesenchyme', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(22997, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0138576', 'decreased cell population proliferation in anatomical structure', 0.4411764705882353, 5.835653092541957, 1.6045413160604438, 'HP:0011017', 'Abnormal cellular physiology'),
(22998, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0101120', 'abnormal cardiac progenitor cell', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(22999, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0127337', 'abnormally localised oxygen accumulating cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(23000, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0100728', 'abnormal cell condensation', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(23001, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0100956', 'abnormal centrosome', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(23002, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0138717', 'decreased cell population proliferation in acellular anatomical structure', 0.4166666666666667, 5.835653092541957, 1.5593338712067029, 'HP:0011017', 'Abnormal cellular physiology'),
(23003, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0127196', 'abnormally localised electrically active cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(23004, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0141777', 'abnormal catabolic process', 0.4782608695652174, 4.758907843651163, 1.508641575552437, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(23005, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0141767', 'abnormal temperature homeostasis', 0.4074074074074074, 4.758907843651163, 1.392413123563799, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(23006, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0141798', 'abnormal lipid metabolic process', 0.44, 4.758907843651163, 1.447038165082909, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(23007, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0101503', 'abnormal organ cortex', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(23008, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0101468', 'abnormal stage I oocyte', 0.5652173913043478, 3.6715585125471644, 1.440565418328227, 'UPHENO:0086172', 'abnormal cell'),
(23009, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0100384', 'abnormal amputated tissue', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(23010, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0107269', 'abnormal right side', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(23011, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0125530', 'absent chondroblast', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(23012, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0141272', 'absent surface breathing', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(23013, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0131389', 'abnormally decreased number of barrier epithelial cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(23014, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0101132', 'abnormal apoptotic cell', 0.6190476190476191, 3.6715585125471644, 1.5076039119696991, 'UPHENO:0086172', 'abnormal cell'),
(23015, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0127435', 'abnormally localised mitotic spindle', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(23016, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0103145', 'abnormal basal body morphology', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(23017, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0131706', 'abnormal ciliary basal body organization', 0.5555555555555556, 5.835653092541957, 1.8005636605953823, 'HP:0011017', 'Abnormal cellular physiology'),
(23018, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0101569', 'abnormal activin-induced ectoderm', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(23019, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0101037', 'abnormal hatching gland cell', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(23020, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0125743', 'absent lampbrush chromosome', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(23021, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0102531', 'abnormal secondary spermatogonium morphology', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(23022, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0131180', 'abnormally decreased number of cell', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(23023, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0101083', 'abnormal T cell', 0.48148148148148145, 3.6715585125471644, 1.3295816755533123, 'UPHENO:0086172', 'abnormal cell'),
(23024, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0133473', 'abnormally decreased number of cilium in the ciliated non-epidermal cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(23025, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0102965', 'abnormal barrier epithelial cell morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(23026, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0139127', 'decreased cell population proliferation in joint region', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(23027, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0101480', 'abnormal stage V oocyte', 0.5652173913043478, 3.6715585125471644, 1.440565418328227, 'UPHENO:0086172', 'abnormal cell'),
(23028, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0141264', 'abnormal schooling behavior', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(23029, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0139619', 'decreased cell population proliferation in basal region', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(23030, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0127171', 'abnormally localised myelin accumulating cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(23031, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0103099', 'abnormal alkali secreting cell morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(23032, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0141911', 'abnormal ribose phosphate metabolic process', 0.4230769230769231, 4.758907843651163, 1.418937661667548, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(23033, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0131153', 'abnormally increased number of electrically active cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(23034, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0101514', 'abnormal dendrite', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(23035, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0101023', 'abnormal ultimobranchial body', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(23036, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0100402', 'abnormal zeugopod', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(23037, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0141782', 'abnormal methylation', 0.4782608695652174, 4.758907843651163, 1.508641575552437, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(23038, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0101467', 'abnormal alkali secreting cell', 0.6190476190476191, 3.6715585125471644, 1.5076039119696991, 'UPHENO:0086172', 'abnormal cell'),
(23039, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0127363', 'abnormally localised barrier cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(23040, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0100398', 'abnormal vegetal blastomere', 0.48148148148148145, 3.6715585125471644, 1.3295816755533123, 'UPHENO:0086172', 'abnormal cell'),
(23041, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0102929', 'abnormal barrier cell morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(23042, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0100427', 'abnormal olfactory system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(23043, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0138577', 'decreased cell population proliferation in anatomical group', 0.4166666666666667, 5.835653092541957, 1.5593338712067029, 'HP:0011017', 'Abnormal cellular physiology'),
(23044, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0133436', 'abnormal cilium morphology in the multiciliated cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(23045, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0101519', 'abnormal hypobranchial placode', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(23046, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0100274', 'abnormal sensory system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(23047, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0139500', 'decreased cell population proliferation in egg jelly', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(23048, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0100915', 'abnormal dermal system', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(23049, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0141776', 'abnormal metabolic process', 0.5238095238095238, 4.758907843651163, 1.5788480773767701, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(23050, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0135479', 'increased cell population proliferation in male organism', 0.4166666666666667, 5.835653092541957, 1.5593338712067029, 'HP:0011017', 'Abnormal cellular physiology'),
(23051, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0135504', 'increased cell population proliferation in multi-tissue structure', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(23052, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0100924', 'abnormal spermatozoon', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(23053, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0100842', 'abnormal left-dorsal blastomere', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(23054, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0131348', 'abnormally decreased number of absorptive cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(23055, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0100511', 'abnormal stylopod', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(23056, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0115512', 'abnormally semi-erect whole organism', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(23057, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0107268', 'abnormal left side', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(23058, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0100337', 'abnormal zygote', 0.6190476190476191, 3.6715585125471644, 1.5076039119696991, 'UPHENO:0086172', 'abnormal cell'),
(23059, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0131569', 'abnormally localised cortical actin cytoskeleton', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(23060, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0141795', 'abnormal glycosylation', 0.44, 4.758907843651163, 1.447038165082909, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(23061, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0131669', 'abnormal Roux spot', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(23062, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0141743', 'abnormal chemical homeostasis within a tissue', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(23063, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0141498', 'abnormal axon microtubule bundle', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(23064, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0136517', 'increased cell population proliferation in basal region', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(23065, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0131031', 'abnormally increased number of nucleate erythrocyte', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(23066, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0100062', 'abnormal anatomical space', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(23067, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0102434', 'abnormal exocrine cell morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(23068, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0102347', 'abnormal ciliated cell morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(23069, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0100954', 'abnormal neural progenitor cell', 0.48148148148148145, 3.6715585125471644, 1.3295816755533123, 'UPHENO:0086172', 'abnormal cell'),
(23070, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0107312', 'abnormal filopodium', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(23071, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0100481', 'abnormal anatomical line', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(23072, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0107399', 'abnormal filopodium morphology', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(23073, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0100416', 'abnormal ligament', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(23074, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0100395', 'abnormal blastomere D1.1', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(23075, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0100509', 'abnormal germ plasm', 0.5, 3.6715585125471644, 1.3549093166236559, 'UPHENO:0086172', 'abnormal cell'),
(23076, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0100108', 'abnormal cell part', 0.6190476190476191, 3.6715585125471644, 1.5076039119696991, 'UPHENO:0086172', 'abnormal cell'),
(23077, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0100152', 'abnormal alimentary system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(23078, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0141789', 'abnormal hormone catabolic process', 0.4074074074074074, 4.758907843651163, 1.392413123563799, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(23079, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0101212', 'abnormal glomeral mesenchyme', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(23080, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0131314', 'abnormally decreased number of exocrine cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(23081, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0100864', 'abnormal dorsolateral ascending neuron', 0.48148148148148145, 3.6715585125471644, 1.3295816755533123, 'UPHENO:0086172', 'abnormal cell'),
(23082, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0101200', 'abnormal joint region', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(23083, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0131654', 'abnormal neuron projection', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(23084, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0100316', 'abnormal gamete', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(23085, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0136516', 'increased cell population proliferation in axial region', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(23086, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0100912', 'abnormal trabecula', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(23087, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0100882', 'abnormal perichondrial cell', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(23088, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0128071', 'decreased size of the cell part', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(23089, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0103129', 'abnormal ciliary axoneme morphology', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(23090, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0107276', 'abnormal dorsal region', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(23091, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0142023', 'absent desmosome', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(23092, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0141267', 'abnormal resting posture', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(23093, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0101096', 'abnormal tendon', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(23094, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0100960', 'abnormal postmigratory neural crest cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(23095, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0127522', 'abnormally localised cementoblast', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(23096, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0102896', 'abnormal mitotic spindle morphology', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(23097, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0100654', 'abnormal blastomere V2.1', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(23098, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0131205', 'abnormally decreased number of ciliated cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(23099, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0127364', 'abnormally localised multiciliated cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(23100, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0131075', 'abnormally increased number of mucus secreting cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(23101, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0100585', 'abnormal elastica externa', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(23102, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0133445', 'abnormally increased number of cilium in the ciliated non-epidermal cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(23103, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0100186', 'abnormal uveal tract', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(23104, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0100069', 'abnormal urinary system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(23105, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0101358', 'abnormal endothelial cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(23106, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0141771', 'abnormal urea homeostasis', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(23107, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0115508', 'abnormally peramorphic growth of whole organism', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(23108, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0100843', 'abnormal fasciculated network of fibrils', 0.5, 3.6715585125471644, 1.3549093166236559, 'UPHENO:0086172', 'abnormal cell'),
(23109, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0126737', 'abnormally localised mesenchymal stem cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(23110, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0100397', 'abnormal ventral vegetal hemisphere blastomere', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(23111, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0101022', 'abnormal blastomere V1.2', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(23112, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0131278', 'abnormally decreased number of keratin accumulating cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(23113, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0127683', 'abnormally localised centromere', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(23114, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0100899', 'abnormal secondary spermatogonium', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(23115, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0102306', 'abnormal secondary oogonium morphology', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(23116, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0107266', 'abnormal dorsal side', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(23117, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0131677', 'abnormal actin filament', 0.5652173913043478, 3.6715585125471644, 1.440565418328227, 'UPHENO:0086172', 'abnormal cell'),
(23118, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0101326', 'abnormal cementoblast', 0.6190476190476191, 3.6715585125471644, 1.5076039119696991, 'UPHENO:0086172', 'abnormal cell'),
(23119, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0103093', 'abnormal sperm entry point morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(23120, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0101071', 'abnormal endoplasmic reticulum', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(23121, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0100003', 'abnormal organism subdivision', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(23122, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0100282', 'abnormal pelvic girdle primordium', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(23123, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0100339', 'abnormal circumblastoporal collar', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(23124, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0100862', 'abnormal blastomere V1', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(23125, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0135507', 'increased cell population proliferation in tissue', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(23126, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0103080', 'abnormal myelin accumulating cell morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(23127, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0138579', 'decreased cell population proliferation in whole organism', 0.42857142857142855, 5.835653092541957, 1.5814531869511603, 'HP:0011017', 'Abnormal cellular physiology'),
(23128, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0100887', 'abnormal right-dorsal blastomere', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(23129, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0125013', 'absent early embryonic cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(23130, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0101347', 'abnormal hindlimb region', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(23131, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0127391', 'abnormally localised lampbrush chromosome', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(23132, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0101061', 'abnormal plasma membrane', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(23133, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0107371', 'abnormal migrating myoblast morphology', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(23134, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0101740', 'abnormal cell part morphology', 0.48148148148148145, 3.6715585125471644, 1.3295816755533123, 'UPHENO:0086172', 'abnormal cell'),
(23135, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0125559', 'absent electrically active cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(23136, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0136028', 'increased cell population proliferation in interdigital region', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(23137, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0101168', 'abnormal circulating cell', 0.52, 3.6715585125471644, 1.3817418089225373, 'UPHENO:0086172', 'abnormal cell'),
(23138, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0136526', 'increased cell population proliferation in postero-ventral region', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(23139, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0102768', 'abnormal ooplasm morphology', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(23140, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0139624', 'decreased cell population proliferation in medial region', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(23141, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0139622', 'decreased cell population proliferation in dorsal region', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(23142, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0127089', 'abnormally localised myoblast', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(23143, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0100533', 'abnormal melanoblast', 0.6190476190476191, 3.6715585125471644, 1.5076039119696991, 'UPHENO:0086172', 'abnormal cell'),
(23144, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0131707', 'abnormal cilium assembly', 0.5172413793103449, 5.835653092541957, 1.7373661832679608, 'HP:0011017', 'Abnormal cellular physiology'),
(23145, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0100035', 'abnormal ventral animal hemisphere blastomere', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(23146, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0130979', 'abnormally increased number of Merkel cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(23147, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0102852', 'abnormal centriole morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(23148, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0101804', 'abnormal stem cell morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(23149, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0141285', 'abnormal cortical actin cytoskeleton morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(23150, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0136567', 'increased cell population proliferation in ventro-lateral region', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(23151, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0126738', 'abnormally localised paracrine cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(23152, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0100164', 'abnormal neural nucleus', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(23153, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0100581', 'abnormal immune system', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(23154, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0100713', 'abnormal monociliated cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(23155, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0101490', 'abnormal ectodermal cell', 0.48148148148148145, 3.6715585125471644, 1.3295816755533123, 'UPHENO:0086172', 'abnormal cell'),
(23156, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0101547', 'abnormal lampbrush chromosome', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(23157, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0100225', 'abnormal endocrine system', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(23158, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0102693', 'abnormal plasma membrane morphology', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(23159, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0101366', 'abnormal morula cell', 0.5652173913043478, 3.6715585125471644, 1.440565418328227, 'UPHENO:0086172', 'abnormal cell'),
(23160, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0100392', 'abnormal cilium', 0.5652173913043478, 3.6715585125471644, 1.440565418328227, 'UPHENO:0086172', 'abnormal cell'),
(23161, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0141714', 'abnormal anterior notochord', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(23162, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0131165', 'abnormally increased number of cementoblast', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(23163, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0141296', 'abnormal adherens junction morphology', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(23164, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0100859', 'abnormal blastomere V1.1.2', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(23165, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0131171', 'abnormally increased number of barrier epithelial cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(23166, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0124884', 'absent keratin accumulating cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(23167, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0100610', 'abnormal appendage', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(23168, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0131354', 'abnormally decreased number of multiciliated cell precursor', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(23169, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0100010', 'abnormal multicellular anatomical structure', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(23170, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0133471', 'abnormally decreased number of cilium in the ciliated cell', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(23171, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0102869', 'abnormal mucus secreting cell morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(23172, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0100547', 'abnormal blastomere V2', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(23173, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0141499', 'abnormal tadpole', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(23174, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0100545', 'abnormal male organism', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(23175, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0125715', 'absent barrier cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(23176, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0138822', 'decreased cell population proliferation in extraembryonic structure', 0.4166666666666667, 5.835653092541957, 1.5593338712067029, 'HP:0011017', 'Abnormal cellular physiology'),
(23177, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0131307', 'abnormally decreased number of mitotic cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(23178, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0127975', 'abnormally localised mitochondrial cloud', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(23179, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0100162', 'abnormal presumptive rhombomere', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(23180, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0103041', 'abnormal perivitelline space morphology', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(23181, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0100295', 'abnormal extracellular matrix', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(23182, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0131561', 'abnormally localised actin filament', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(23183, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0141860', 'abnormal malate-aspartate shuttle', 0.4583333333333333, 4.758907843651163, 1.4768771428276568, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(23184, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0138715', 'decreased cell population proliferation in anatomical cluster', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(23185, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0124984', 'absent progenitor cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(23186, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0141263', 'abnormal visually guided collision avoidance behavior', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(23187, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0101374', 'abnormal migratory neural crest cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(23188, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0100742', 'abnormal musculoskeletal system', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(23189, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0141904', 'abnormal glucosamine metabolic process', 0.4782608695652174, 4.758907843651163, 1.508641575552437, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(23190, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0127018', 'abnormally localised ciliated cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(23191, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0136478', 'increased cell population proliferation in thoracic region', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(23192, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0100034', 'abnormal blastomere V1.1', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(23193, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0103179', 'abnormal lampbrush chromosome morphology', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(23194, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0136398', 'increased cell population proliferation in egg jelly', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(23195, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0141784', 'abnormal cellular hormone metabolic process', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(23196, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0103021', 'abnormal wedge region morphology', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(23197, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0100642', 'abnormal gustatory system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(23198, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0126162', 'absent alkali secreting cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(23199, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0101166', 'abnormal premigratory neural crest cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(23200, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0100791', 'abnormal multiciliated cell precursor', 0.6190476190476191, 3.6715585125471644, 1.5076039119696991, 'UPHENO:0086172', 'abnormal cell'),
(23201, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0100521', 'abnormal animal blastomere', 0.48148148148148145, 3.6715585125471644, 1.3295816755533123, 'UPHENO:0086172', 'abnormal cell'),
(23202, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0139628', 'decreased cell population proliferation in postero-ventral region', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(23203, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0102958', 'abnormal cementoblast morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(23204, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0135613', 'increased cell population proliferation in anatomical cluster', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(23205, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0136518', 'increased cell population proliferation in anterior region', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(23206, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0135509', 'increased cell population proliferation in embryonic structure', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(23207, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0101110', 'abnormal cell-free extract', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(23208, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0115391', 'abnormally undifferentiated alimentary system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(23209, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0135482', 'increased cell population proliferation in cell', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(23210, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0141511', 'abnormally localised nucleus in myoblast', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(23211, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0101576', 'abnormal blastomere V1.2.2', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(23212, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0100196', 'abnormal neuron', 0.5, 3.6715585125471644, 1.3549093166236559, 'UPHENO:0086172', 'abnormal cell'),
(23213, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0141265', 'abnormal escape behavior', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(23214, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0100520', 'abnormal blastomere D1.2', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(23215, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0131735', 'abnormal spindle assembly', 0.5714285714285714, 10.281312506061912, 2.4238472967061404, 'HP:0002916', 'Abnormality of chromosome segregation'),
(23216, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0131691', 'abnormal molecular function', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(23217, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0107311', 'abnormal apical junction complex', 0.5, 3.6715585125471644, 1.3549093166236559, 'UPHENO:0086172', 'abnormal cell'),
(23218, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0101004', 'abnormal acid secreting cell', 0.6190476190476191, 3.6715585125471644, 1.5076039119696991, 'UPHENO:0086172', 'abnormal cell'),
(23219, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0100515', 'abnormal somatic stem cell', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(23220, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0102588', 'abnormal centrosome morphology', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(23221, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0100372', 'abnormal hematological system', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(23222, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0103037', 'abnormal ring structure morphology', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(23223, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0100175', 'abnormal migrating neuroblast', 0.5, 3.6715585125471644, 1.3549093166236559, 'UPHENO:0086172', 'abnormal cell'),
(23224, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0101389', 'abnormal wedge region', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(23225, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0100667', 'abnormal vegetal yolk mass', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(23226, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0107426', 'abnormal yolk platelet morphology', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(23227, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0133438', 'abnormal cilium morphology in the ciliated non-epidermal cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(23228, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0130968', 'abnormally increased number of early embryonic cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(23229, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0101969', 'abnormal zygote morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(23230, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0103414', 'abnormally increased number of vacuole in the spermatozoon', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(23231, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0100802', 'abnormal exocrine cell', 0.6190476190476191, 3.6715585125471644, 1.5076039119696991, 'UPHENO:0086172', 'abnormal cell'),
(23232, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0135475', 'increased cell population proliferation in anatomical group', 0.4166666666666667, 5.835653092541957, 1.5593338712067029, 'HP:0011017', 'Abnormal cellular physiology'),
(23233, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0100900', 'abnormal angioblast', 0.52, 3.6715585125471644, 1.3817418089225373, 'UPHENO:0086172', 'abnormal cell'),
(23234, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0101094', 'abnormal blastomere V2.2.1', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(23235, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0101463', 'abnormal right-ventral blastomere', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(23236, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0102423', 'abnormal multiciliated cell precursor morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(23237, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0135718', 'increased cell population proliferation in anatomical line', 0.4411764705882353, 5.835653092541957, 1.6045413160604438, 'HP:0011017', 'Abnormal cellular physiology'),
(23238, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0103636', 'abnormally increased number of melanoblast', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(23239, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0141276', 'decreased surface breathing', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(23240, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0135615', 'increased cell population proliferation in acellular anatomical structure', 0.4166666666666667, 5.835653092541957, 1.5593338712067029, 'HP:0011017', 'Abnormal cellular physiology'),
(23241, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0102608', 'abnormal multiciliated cell morphology', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(23242, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0107260', 'abnormal anterior-posterior axis', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(23243, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0127476', 'abnormally localised nucleus', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(23244, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0100014', 'abnormal tissue', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(23245, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0100026', 'abnormal germ cell', 0.6190476190476191, 3.6715585125471644, 1.5076039119696991, 'UPHENO:0086172', 'abnormal cell'),
(23246, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0141792', 'abnormal small molecule metabolic process', 0.4782608695652174, 4.758907843651163, 1.508641575552437, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(23247, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0131004', 'abnormally increased number of proepicardium', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(23248, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0100251', 'abnormal proteinaceous extracellular matrix', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(23249, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0101411', 'abnormal marginal zone (sensu neural)', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(23250, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0100285', 'abnormal progenitor cell', 0.6190476190476191, 3.6715585125471644, 1.5076039119696991, 'UPHENO:0086172', 'abnormal cell'),
(23251, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0101518', 'abnormal B cell', 0.48148148148148145, 3.6715585125471644, 1.3295816755533123, 'UPHENO:0086172', 'abnormal cell'),
(23252, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0100817', 'abnormal intersomitic neuron', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(23253, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0100114', 'abnormal peripheral nervous system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(23254, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0125785', 'absent mitotic spindle', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(23255, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0100104', 'abnormal embryonic structure', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(23256, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0141787', 'abnormal hormone metabolic process', 0.4782608695652174, 4.758907843651163, 1.508641575552437, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(23257, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0100396', 'abnormal dorsal animal hemisphere blastomere', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(23258, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0127257', 'abnormally localised wedge region', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(23259, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0100991', 'abnormal iliac process primordium', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(23260, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0136522', 'increased cell population proliferation in medial region', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(23261, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0107267', 'abnormal ventral side', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(23262, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0101345', 'abnormal ascending interneuron', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(23263, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0131204', 'abnormally decreased number of pericyte', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(23264, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0131145', 'abnormally increased number of polar body', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(23265, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0131300', 'abnormally decreased number of alkali secreting cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(23266, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0141797', 'abnormal hydrogen metabolic process', 0.4782608695652174, 4.758907843651163, 1.508641575552437, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(23267, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0100218', 'abnormal epithelial cell', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(23268, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0127643', 'abnormally localised somatic stem cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(23269, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0131096', 'abnormally increased number of exocrine cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(23270, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0125384', 'absent ciliated cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(23271, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0107303', 'abnormal migratory trunk neural crest cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(23272, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0131667', 'abnormal actin cytoskeleton', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(23273, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0141880', 'abnormal ethanolamine metabolic process', 0.4074074074074074, 4.758907843651163, 1.392413123563799, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(23274, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0138611', 'decreased cell population proliferation in embryonic structure', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(23275, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0101504', 'abnormal blastomere D2.2.1', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(23276, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0103104', 'abnormal zygote cortex morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(23277, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0126630', 'abnormally localised early embryonic cell', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(23278, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0100205', 'abnormal limb segment', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(23279, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0141796', 'abnormal demethylation', 0.4782608695652174, 4.758907843651163, 1.508641575552437, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(23280, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0125997', 'absent Merkel cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(23281, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0141794', 'abnormal prosthetic group metabolic process', 0.4782608695652174, 4.758907843651163, 1.508641575552437, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(23282, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0127399', 'abnormally localised melanoblast', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(23283, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0127288', 'abnormally localised pericyte', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(23284, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0142051', 'abnormal cerebrospinal fluid', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(23285, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0127217', 'abnormally localised cilium', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(23286, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0141438', 'increased cell population proliferation in tadpole', 0.4166666666666667, 5.835653092541957, 1.5593338712067029, 'HP:0011017', 'Abnormal cellular physiology'),
(23287, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0100415', 'abnormal secretory epithelial cell', 0.52, 3.6715585125471644, 1.3817418089225373, 'UPHENO:0086172', 'abnormal cell'),
(23288, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0138609', 'decreased cell population proliferation in tissue', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(23289, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0107324', 'abnormal embryonic thrombocyte', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(23290, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0100477', 'abnormal pericyte', 0.6190476190476191, 3.6715585125471644, 1.5076039119696991, 'UPHENO:0086172', 'abnormal cell'),
(23291, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0131708', 'abnormal cilium disassembly', 0.5555555555555556, 5.835653092541957, 1.8005636605953823, 'HP:0011017', 'Abnormal cellular physiology'),
(23292, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0107253', 'abnormal enteric nervous system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(23293, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0124807', 'absent cell part', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(23294, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0125644', 'absent pericyte', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(23295, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0101450', 'abnormal myeloid cell', 0.5, 3.6715585125471644, 1.3549093166236559, 'UPHENO:0086172', 'abnormal cell'),
(23296, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0138838', 'decreased cell population proliferation in cell condensation', 0.4166666666666667, 5.835653092541957, 1.5593338712067029, 'HP:0011017', 'Abnormal cellular physiology'),
(23297, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0138738', 'decreased cell population proliferation in anatomical region', 0.4166666666666667, 5.835653092541957, 1.5593338712067029, 'HP:0011017', 'Abnormal cellular physiology'),
(23298, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0101451', 'abnormal dorsal lymph space', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(23299, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0101917', 'abnormal progenitor cell morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(23300, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0131130', 'abnormally increased number of myelin accumulating cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(23301, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0100701', 'abnormal microglial cell', 0.48148148148148145, 3.6715585125471644, 1.3295816755533123, 'UPHENO:0086172', 'abnormal cell'),
(23302, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0103894', 'abnormally decreased number of spindle microtubule', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(23303, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0129551', 'increased size of the cell part', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(23304, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0100969', 'abnormal disaggregated/reaggregated ectoderm treated with activin', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(23305, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0115758', 'abnormally decreased mobility of melanoblast', 0.52, 3.6715585125471644, 1.3817418089225373, 'UPHENO:0086172', 'abnormal cell'),
(23306, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0139423', 'decreased cell population proliferation in multicellular anatomical structure', 0.4166666666666667, 5.835653092541957, 1.5593338712067029, 'HP:0011017', 'Abnormal cellular physiology'),
(23307, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0131134', 'abnormally increased number of barrier cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(23308, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0100449', 'abnormal lymphocyte', 0.5, 3.6715585125471644, 1.3549093166236559, 'UPHENO:0086172', 'abnormal cell'),
(23309, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0100599', 'abnormal adult immune system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(23310, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0126495', 'abnormally localised keratin accumulating cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(23311, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0100721', 'abnormal centromere', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(23312, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0131283', 'abnormally decreased number of myoblast', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(23313, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0124864', 'absent germ cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(23314, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0127372', 'abnormally localised polar body', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(23315, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0100852', 'abnormal interdigital region', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(23316, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0116434', 'abnormal biological process', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(23317, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0101176', 'abnormal non-ciliated epithelial cell', 0.52, 3.6715585125471644, 1.3817418089225373, 'UPHENO:0086172', 'abnormal cell'),
(23318, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0136191', 'increased cell population proliferation in organ part', 0.42857142857142855, 5.835653092541957, 1.5814531869511603, 'HP:0011017', 'Abnormal cellular physiology'),
(23319, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0101350', 'abnormal blastomere D2.1.2', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(23320, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0100732', 'abnormal tendon fibroblast', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(23321, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0142057', 'abnormal desmosome', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(23322, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0100273', 'abnormal visual system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(23323, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0141791', 'abnormal primary metabolic process', 0.4782608695652174, 4.758907843651163, 1.508641575552437, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(23324, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0141718', 'abnormal posterior notochord', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(23325, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0124845', 'absent stem cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(23326, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0100465', 'abnormal skeletal system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(23327, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0125061', 'absent basal body', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(23328, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0136519', 'increased cell population proliferation in posterior region', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(23329, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0100394', 'abnormal marginal zone', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(23330, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0139621', 'decreased cell population proliferation in posterior region', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(23331, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0125693', 'absent mucus secreting cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(23332, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0101240', 'abnormal ciliated non-epidermal cell', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(23333, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0101534', 'abnormal blastomere V2.1.1', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(23334, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0100344', 'abnormal portion of organism substance', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(23335, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0126314', 'absent absorptive cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(23336, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0135736', 'increased cell population proliferation in cell condensation', 0.4166666666666667, 5.835653092541957, 1.5593338712067029, 'HP:0011017', 'Abnormal cellular physiology'),
(23337, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0107323', 'abnormal thrombocyte', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(23338, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0131346', 'abnormally decreased number of chondroblast', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(23339, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0107264', 'abnormal anterior side', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(23340, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0100913', 'abnormal Brachets cleft', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(23341, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0126681', 'abnormally localised basal body', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(23342, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0102285', 'abnormal myoblast morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(23343, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0101009', 'abnormal blastomere D1.1.1', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(23344, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0100894', 'abnormal nucleus', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(23345, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0102636', 'abnormal acid secreting cell morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(23346, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0131694', 'abnormal RNA polymerase II activity', 0.4230769230769231, 4.758907843651163, 1.418937661667548, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(23347, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0136525', 'increased cell population proliferation in postero-dorsal region', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(23348, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0116091', 'abnormally increased variability of size of cell in endoderm', 0.48148148148148145, 3.6715585125471644, 1.3295816755533123, 'UPHENO:0086172', 'abnormal cell'),
(23349, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0135474', 'increased cell population proliferation in anatomical structure', 0.4411764705882353, 5.835653092541957, 1.6045413160604438, 'HP:0011017', 'Abnormal cellular physiology'),
(23350, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0127520', 'abnormally localised gastrula cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(23351, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0127168', 'abnormally localised chondroblast', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(23352, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0135742', 'increased cell population proliferation in extracellular matrix', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(23353, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0141315', 'abnormal anatomical region', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(23354, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0100293', 'abnormal duct', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(23355, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0101657', 'abnormal oocyte morphology', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(23356, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0138606', 'decreased cell population proliferation in multi-tissue structure', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(23357, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0141421', 'decreased cell population proliferation in tadpole', 0.4166666666666667, 5.835653092541957, 1.5593338712067029, 'HP:0011017', 'Abnormal cellular physiology'),
(23358, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0100574', 'abnormal gastrula cell', 0.5652173913043478, 3.6715585125471644, 1.440565418328227, 'UPHENO:0086172', 'abnormal cell'),
(23359, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0138232', 'decreased cell population proliferation in forelimb region', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(23360, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0100781', 'abnormal presumptive ectoderm', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(23361, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0100807', 'abnormal matrix-based tissue', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(23362, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0100745', 'abnormal anterior lymph sac', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(23363, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0101333', 'abnormal barrier epithelial cell', 0.6190476190476191, 3.6715585125471644, 1.5076039119696991, 'UPHENO:0086172', 'abnormal cell'),
(23364, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0131248', 'abnormally decreased number of acid secreting cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(23365, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0126454', 'abnormally localised stem cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(23366, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0138424', 'decreased cell population proliferation in marginal zone (sensu neural)', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(23367, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0131189', 'abnormally decreased number of stem cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(23368, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0138584', 'decreased cell population proliferation in cell', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(23369, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0124934', 'absent centrosome', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(23370, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0101378', 'abnormal blastomere D1', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(23371, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0138820', 'decreased cell population proliferation in anatomical line', 0.4411764705882353, 5.835653092541957, 1.6045413160604438, 'HP:0011017', 'Abnormal cellular physiology'),
(23372, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0100557', 'abnormal prime meridian', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(23373, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0131129', 'abnormally increased number of chondroblast', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(23374, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0131675', 'abnormal spindle microtubule', 0.5652173913043478, 3.6715585125471644, 1.440565418328227, 'UPHENO:0086172', 'abnormal cell'),
(23375, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0141898', 'abnormal maltose metabolic process', 0.4230769230769231, 4.758907843651163, 1.418937661667548, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(23376, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0100551', 'abnormal oocyte cortex', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(23377, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0100009', 'abnormal multi-tissue structure', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(23378, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0131687', 'abnormal astral microtubule', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(23379, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0139627', 'decreased cell population proliferation in postero-dorsal region', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(23380, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0100902', 'abnormal spermatocyte', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(23381, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0103631', 'abnormally increased number of apoptotic cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(23382, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0141497', 'abnormal lymphoblast', 0.5, 3.6715585125471644, 1.3549093166236559, 'UPHENO:0086172', 'abnormal cell'),
(23383, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0100814', 'abnormal natural killer cell', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(23384, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0100429', 'abnormal spermatid', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(23385, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0131202', 'abnormally decreased number of germ cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(23386, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0141289', 'abnormal spindle microtubule morphology', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(23387, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0127794', 'abnormally localised mitotic cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(23388, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0127338', 'abnormally localised mucus secreting cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(23389, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0135476', 'increased cell population proliferation in anatomical system', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(23390, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0125750', 'absent melanoblast', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(23391, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0103067', 'abnormal paracrine cell morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(23392, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0135160', 'increased cell population proliferation in embryo', 0.4166666666666667, 5.835653092541957, 1.5593338712067029, 'HP:0011017', 'Abnormal cellular physiology'),
(23393, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0102323', 'abnormal keratin accumulating cell morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(23394, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0102069', 'abnormal proepicardium morphology', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(23395, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0107258', 'abnormal anatomical axis', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(23396, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0101515', 'abnormal neuromast mantle cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(23397, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0126628', 'abnormally localised blastomere', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(23398, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0135478', 'increased cell population proliferation in female organism', 0.4166666666666667, 5.835653092541957, 1.5593338712067029, 'HP:0011017', 'Abnormal cellular physiology'),
(23399, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0125859', 'absent nucleate erythrocyte', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(23400, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0100332', 'abnormal germinal granule', 0.48148148148148145, 3.6715585125471644, 1.3295816755533123, 'UPHENO:0086172', 'abnormal cell'),
(23401, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0101373', 'abnormal oxygen accumulating cell', 0.6190476190476191, 3.6715585125471644, 1.5076039119696991, 'UPHENO:0086172', 'abnormal cell'),
(23402, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0101311', 'abnormal bottle cell', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(23403, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0131371', 'abnormally decreased number of electrically active cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(23404, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0138262', 'decreased cell population proliferation in embryo', 0.4166666666666667, 5.835653092541957, 1.5593338712067029, 'HP:0011017', 'Abnormal cellular physiology'),
(23405, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0100823', 'abnormal blood', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(23406, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0101435', 'abnormal paracrine cell', 0.6190476190476191, 3.6715585125471644, 1.5076039119696991, 'UPHENO:0086172', 'abnormal cell'),
(23407, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0135636', 'increased cell population proliferation in anatomical region', 0.4166666666666667, 5.835653092541957, 1.5593338712067029, 'HP:0011017', 'Abnormal cellular physiology'),
(23408, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0127533', 'abnormally localised spermatocyte', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(23409, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0100202', 'abnormal embryo', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(23410, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0126725', 'abnormally localised epithelial cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(23411, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0102872', 'abnormal ciliated non-epidermal cell morphology', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(23412, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0139669', 'decreased cell population proliferation in ventro-lateral region', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(23413, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0127160', 'abnormally localised acid secreting cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(23414, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0100861', 'abnormal blastomere D2.2.2', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(23415, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0126214', 'absent microtubule', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(23416, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0100203', 'abnormal endocrine cell', 0.5, 3.6715585125471644, 1.3549093166236559, 'UPHENO:0086172', 'abnormal cell'),
(23417, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0131553', 'abnormally localised Roux spot', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(23418, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0101228', 'abnormal mesenchymal stem cell', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(23419, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0138233', 'decreased cell population proliferation in hindlimb region', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(23420, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0100917', 'abnormal stage III oocyte', 0.5652173913043478, 3.6715585125471644, 1.440565418328227, 'UPHENO:0086172', 'abnormal cell'),
(23421, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0131247', 'abnormally decreased number of nucleate erythrocyte', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(23422, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0142052', 'abnormal nasal region', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(23423, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0100569', 'abnormal motor axon', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(23424, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0142066', 'abnormally increased number of desmosome', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(23425, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0103167', 'abnormal absorptive cell morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(23426, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0100544', 'abnormal neuromast support cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(23427, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0131089', 'abnormally increased number of mitotic cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(23428, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0125868', 'absent cementoblast', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(23429, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0101658', 'abnormal germ cell morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(23430, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0141781', 'abnormal secondary metabolic process', 0.4782608695652174, 4.758907843651163, 1.508641575552437, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(23431, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0116494', 'absent biological process', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(23432, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0139717', 'abnormally necrotic cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(23433, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0100239', 'abnormal acellular anatomical structure', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(23434, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0101220', 'abnormal centriole', 0.5652173913043478, 3.6715585125471644, 1.440565418328227, 'UPHENO:0086172', 'abnormal cell'),
(23435, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0125692', 'absent oxygen accumulating cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(23436, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0139130', 'decreased cell population proliferation in interdigital region', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(23437, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0101921', 'abnormal chondroblast morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(23438, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0101325', 'abnormal blastomere D2.1.1', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(23439, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0100031', 'abnormal central nervous system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(23440, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0133443', 'abnormally increased number of cilium in the multiciliated cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(23441, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0138581', 'decreased cell population proliferation in male organism', 0.4166666666666667, 5.835653092541957, 1.5593338712067029, 'HP:0011017', 'Abnormal cellular physiology'),
(23442, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0101269', 'abnormal mesodermal cell', 0.48148148148148145, 3.6715585125471644, 1.3295816755533123, 'UPHENO:0086172', 'abnormal cell'),
(23443, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0102539', 'abnormal cytoplasm morphology', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(23444, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0102183', 'abnormal oocyte cortex morphology', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(23445, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0125854', 'absent barrier epithelial cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(23446, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0100028', 'abnormal anatomical cluster', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(23447, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0138890', 'decreased cell population proliferation in intersomitic region', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(23448, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0135483', 'increased cell population proliferation in organism subdivision', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(23449, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0135720', 'increased cell population proliferation in extraembryonic structure', 0.4166666666666667, 5.835653092541957, 1.5593338712067029, 'HP:0011017', 'Abnormal cellular physiology'),
(23450, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0125779', 'absent endoplasmic reticulum', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(23451, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0100437', 'abnormal proepicardium', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(23452, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0101162', 'abnormal stromal cell', 0.48148148148148145, 3.6715585125471644, 1.3295816755533123, 'UPHENO:0086172', 'abnormal cell'),
(23453, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0101362', 'abnormal vegetal cortex', 0.52, 3.6715585125471644, 1.3817418089225373, 'UPHENO:0086172', 'abnormal cell'),
(23454, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0100733', 'abnormal fibroblast', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(23455, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0102873', 'abnormal nucleate erythrocyte morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(23456, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0100422', 'abnormal notochord', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(23457, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0141277', 'abnormal actin cytoskeleton morphology', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(23458, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0100176', 'abnormal stage VI oocyte', 0.5652173913043478, 3.6715585125471644, 1.440565418328227, 'UPHENO:0086172', 'abnormal cell'),
(23459, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0101587', 'abnormal hemangioblast', 0.5, 3.6715585125471644, 1.3549093166236559, 'UPHENO:0086172', 'abnormal cell'),
(23460, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0131383', 'abnormally decreased number of cementoblast', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(23461, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0135716', 'increased cell population proliferation in portion of organism substance', 0.4411764705882353, 5.835653092541957, 1.6045413160604438, 'HP:0011017', 'Abnormal cellular physiology'),
(23462, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0102526', 'abnormal nucleus morphology', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(23463, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0100172', 'abnormal stem cell', 0.6190476190476191, 3.6715585125471644, 1.5076039119696991, 'UPHENO:0086172', 'abnormal cell'),
(23464, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0100501', 'abnormal urogenital system', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(23465, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0101239', 'abnormal olfactory epithelial support cell', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(23466, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0107287', 'abnormal afferent neuron', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(23467, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0141748', 'abnormal gas homeostasis', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(23468, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0127029', 'abnormally localised multiciliated cell precursor', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(23469, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0101078', 'abnormal mucous gland', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(23470, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0100493', 'abnormal liver and biliary system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(23471, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0115509', 'abnormally semi-viable whole organism', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(23472, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0102181', 'abnormal mitotic cell morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(23473, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0141790', 'abnormal cellular metabolic process', 0.4583333333333333, 4.758907843651163, 1.4768771428276568, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(23474, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0100587', 'abnormal vestibuloauditory system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(23475, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0101452', 'abnormal blastomere V1.1.1', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(23476, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0100032', 'abnormal nervous system', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(23477, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0102356', 'abnormal kinetochore morphology', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(23478, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0136523', 'increased cell population proliferation in antero-dorsal region', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(23479, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:00000000', 'Xenopus phenotype', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(23480, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0127896', 'abnormally localised ring structure', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(23481, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0102534', 'abnormal spermatocyte morphology', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(23482, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0102386', 'abnormal electrically active cell morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(23483, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0131523', 'absent actin filament', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(23484, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0127703', 'abnormally localised morula cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(23485, 'HP:0002916', 'Abnormality of chromosome segregation', 'XPO:0131347', 'abnormally decreased number of myelin accumulating cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
