(462648, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0125644', 'absent pericyte', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(462649, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0100707', 'abnormal central vegetal yolk mass', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(462650, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0101500', 'abnormal endodermal cell', 0.5, 3.6715585125471644, 1.3549093166236559, 'UPHENO:0086172', 'abnormal cell'),
(462651, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0124934', 'absent centrosome', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(462652, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0141271', 'increased surface breathing', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(462653, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0100403', 'abnormal forelimb', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(462654, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0100186', 'abnormal uveal tract', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(462655, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0101200', 'abnormal joint region', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(462656, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0100175', 'abnormal migrating neuroblast', 0.52, 3.6715585125471644, 1.3817418089225373, 'UPHENO:0086172', 'abnormal cell'),
(462657, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0107312', 'abnormal filopodium', 0.6190476190476191, 3.6715585125471644, 1.5076039119696991, 'UPHENO:0086172', 'abnormal cell'),
(462658, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0107323', 'abnormal thrombocyte', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(462659, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0100114', 'abnormal peripheral nervous system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(462660, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0141264', 'abnormal schooling behavior', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(462661, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0100482', 'abnormal Mullerian duct', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(462662, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0141794', 'abnormal prosthetic group metabolic process', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(462663, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0131308', 'abnormally decreased number of oxygen accumulating cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(462664, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0101481', 'abnormal skeletal muscle satellite cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(462665, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0125698', 'absent filopodium', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(462666, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0100028', 'abnormal anatomical cluster', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(462667, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0100295', 'abnormal extracellular matrix', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(462668, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0100856', 'abnormal simple organ', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(462669, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0131307', 'abnormally decreased number of mitotic cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(462670, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0101480', 'abnormal stage V oocyte', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(462671, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0100429', 'abnormal spermatid', 0.6190476190476191, 3.6715585125471644, 1.5076039119696991, 'UPHENO:0086172', 'abnormal cell'),
(462672, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0100437', 'abnormal proepicardium', 0.6190476190476191, 3.6715585125471644, 1.5076039119696991, 'UPHENO:0086172', 'abnormal cell'),
(462673, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0100570', 'abnormal axon', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(462674, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0100549', 'abnormal mitotic cell', 0.65, 3.6715585125471644, 1.5448343060521594, 'UPHENO:0086172', 'abnormal cell'),
(462675, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0126079', 'absent yolk platelet', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(462676, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0100384', 'abnormal amputated tissue', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(462677, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0131153', 'abnormally increased number of electrically active cell', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(462678, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0101535', 'abnormal absorptive cell', 0.65, 3.6715585125471644, 1.5448343060521594, 'UPHENO:0086172', 'abnormal cell'),
(462679, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0101132', 'abnormal apoptotic cell', 0.65, 3.6715585125471644, 1.5448343060521594, 'UPHENO:0086172', 'abnormal cell'),
(462680, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0100688', 'abnormal adipose tissue', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(462681, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0100069', 'abnormal urinary system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(462682, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0125533', 'absent myelin accumulating cell', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(462683, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0100852', 'abnormal interdigital region', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(462684, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0103414', 'abnormally increased number of vacuole in the spermatozoon', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(462685, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0100006', 'abnormal anatomical structure', 0.5294117647058824, 1.706362323152461, 0.9504568842024205, 'UPHENO:0002536', 'abnormal anatomical entity'),
(462686, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0125833', 'absent kinetochore', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(462687, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0100282', 'abnormal pelvic girdle primordium', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(462688, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0127196', 'abnormally localised electrically active cell', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(462689, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0100732', 'abnormal tendon fibroblast', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(462690, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0101239', 'abnormal olfactory epithelial support cell', 0.48148148148148145, 3.6715585125471644, 1.3295816755533123, 'UPHENO:0086172', 'abnormal cell'),
(462691, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0102069', 'abnormal proepicardium morphology', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(462692, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0131028', 'abnormally increased number of mesenchymal stem cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(462693, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0142064', 'abnormal desmosome morphology', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(462694, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0126600', 'abnormally localised progenitor cell', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(462695, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0100781', 'abnormal presumptive ectoderm', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(462696, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0102183', 'abnormal oocyte cortex morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(462697, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0100721', 'abnormal centromere', 0.6190476190476191, 3.6715585125471644, 1.5076039119696991, 'UPHENO:0086172', 'abnormal cell'),
(462698, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0100915', 'abnormal dermal system', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(462699, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0125854', 'absent barrier epithelial cell', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(462700, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0101157', 'abnormal female organism', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(462701, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0102706', 'abnormal germinal vesicle morphology', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(462702, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0100900', 'abnormal angioblast', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(462703, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0100176', 'abnormal stage VI oocyte', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(462704, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0130973', 'abnormally increased number of stem cell', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(462705, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0100588', 'abnormal unicellular gland', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(462706, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0127821', 'abnormally localised apoptotic cell', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(462707, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0100890', 'abnormal pharyngeal cavity', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(462708, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0107260', 'abnormal anterior-posterior axis', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(462709, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0100393', 'abnormal involuting marginal zone', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(462710, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0141770', 'abnormal urate homeostasis', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(462711, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0115615', 'abnormally posteriorly mislocalised primordial germ cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(462712, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0101168', 'abnormal circulating cell', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(462713, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0102024', 'abnormal cilium morphology', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(462714, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0115512', 'abnormally semi-erect whole organism', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(462715, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0141715', 'abnormal septum', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(462716, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0100503', 'abnormal blastomere D2', 0.5652173913043478, 3.6715585125471644, 1.440565418328227, 'UPHENO:0086172', 'abnormal cell'),
(462717, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0131707', 'abnormal cilium assembly', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(462718, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0102994', 'abnormal vegetal cortex morphology', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(462719, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0100104', 'abnormal embryonic structure', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(462720, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0127486', 'abnormally localised kinetochore', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(462721, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0101099', 'abnormal ventro-lateral marginal zone', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(462722, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0127794', 'abnormally localised mitotic cell', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(462723, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0131098', 'abnormally increased number of multiciliated cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(462724, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0101345', 'abnormal ascending interneuron', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(462725, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0125715', 'absent barrier cell', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(462726, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0127703', 'abnormally localised morula cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(462727, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0100308', 'abnormal early embryonic cell', 0.6190476190476191, 3.6715585125471644, 1.5076039119696991, 'UPHENO:0086172', 'abnormal cell'),
(462728, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0100317', 'abnormal respiratory system', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(462729, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0141277', 'abnormal actin cytoskeleton morphology', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(462730, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0100135', 'abnormal surface structure', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(462731, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0101494', 'abnormal blastomere D1.2.1', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(462732, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0101405', 'abnormal ring structure', 0.5652173913043478, 3.6715585125471644, 1.440565418328227, 'UPHENO:0086172', 'abnormal cell'),
(462733, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0127288', 'abnormally localised pericyte', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(462734, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0141790', 'abnormal cellular metabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(462735, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0139717', 'abnormally necrotic cell', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(462736, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0101411', 'abnormal marginal zone (sensu neural)', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(462737, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0100423', 'abnormal process', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(462738, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0102768', 'abnormal ooplasm morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(462739, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0100691', 'abnormal keratin accumulating cell', 0.65, 3.6715585125471644, 1.5448343060521594, 'UPHENO:0086172', 'abnormal cell'),
(462740, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0101636', 'abnormal cell morphology', 0.48148148148148145, 3.6715585125471644, 1.3295816755533123, 'UPHENO:0086172', 'abnormal cell'),
(462741, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0103636', 'abnormally increased number of melanoblast', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(462742, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0101120', 'abnormal cardiac progenitor cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(462743, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0126628', 'abnormally localised blastomere', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(462744, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0101187', 'abnormal dorsolateral commissural neuron', 0.5, 3.6715585125471644, 1.3549093166236559, 'UPHENO:0086172', 'abnormal cell'),
(462745, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0101560', 'abnormal compound organ component', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(462746, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0101358', 'abnormal endothelial cell', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(462747, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0131189', 'abnormally decreased number of stem cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(462748, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0126495', 'abnormally localised keratin accumulating cell', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(462749, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0100309', 'abnormal vegetal hemisphere', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(462750, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0101389', 'abnormal wedge region', 0.5652173913043478, 3.6715585125471644, 1.440565418328227, 'UPHENO:0086172', 'abnormal cell'),
(462751, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0127522', 'abnormally localised cementoblast', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(462752, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0101591', 'abnormal xanthophore', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(462753, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0141781', 'abnormal secondary metabolic process', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(462754, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0107269', 'abnormal right side', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(462755, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0100133', 'abnormal solid compound organ', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(462756, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0127819', 'abnormally localised ciliary axoneme', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(462757, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0131204', 'abnormally decreased number of pericyte', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(462758, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0100396', 'abnormal dorsal animal hemisphere blastomere', 0.48148148148148145, 3.6715585125471644, 1.3295816755533123, 'UPHENO:0086172', 'abnormal cell'),
(462759, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0127217', 'abnormally localised cilium', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(462760, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0127337', 'abnormally localised oxygen accumulating cell', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(462761, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0127476', 'abnormally localised nucleus', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(462762, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0115508', 'abnormally peramorphic growth of whole organism', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(462763, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0100846', 'abnormal hindlimb', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(462764, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0100902', 'abnormal spermatocyte', 0.6190476190476191, 3.6715585125471644, 1.5076039119696991, 'UPHENO:0086172', 'abnormal cell'),
(462765, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0101098', 'abnormal mineralized extracellular matrix', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(462766, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0100261', 'abnormal multilaminar epithelium', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(462767, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0100386', 'abnormal limb', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(462768, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0103237', 'absent primordial germ cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(462769, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0102347', 'abnormal ciliated cell morphology', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(462770, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0126697', 'abnormally localised proepicardium', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(462771, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0131389', 'abnormally decreased number of barrier epithelial cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(462772, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0131512', 'absent adherens junction', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(462773, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0131351', 'abnormally decreased number of apoptotic cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(462774, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0127631', 'abnormally localised centriole', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(462775, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0100960', 'abnormal postmigratory neural crest cell', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(462776, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0141772', 'abnormal water homeostasis', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(462777, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0100339', 'abnormal circumblastoporal collar', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(462778, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0133438', 'abnormal cilium morphology in the ciliated non-epidermal cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(462779, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0130997', 'abnormally increased number of oocyte', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(462780, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0100392', 'abnormal cilium', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(462781, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0102520', 'abnormal microtubule morphology', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(462782, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0107276', 'abnormal dorsal region', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(462783, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0102852', 'abnormal centriole morphology', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(462784, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0141276', 'decreased surface breathing', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(462785, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0141745', 'abnormal creatinine homeostasis', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(462786, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0131064', 'abnormally increased number of spermatocyte', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(462787, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0101366', 'abnormal morula cell', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(462788, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0101228', 'abnormal mesenchymal stem cell', 0.6190476190476191, 3.6715585125471644, 1.5076039119696991, 'UPHENO:0086172', 'abnormal cell'),
(462789, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0100859', 'abnormal blastomere V1.1.2', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(462790, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0101269', 'abnormal mesodermal cell', 0.5, 3.6715585125471644, 1.3549093166236559, 'UPHENO:0086172', 'abnormal cell'),
(462791, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0131278', 'abnormally decreased number of keratin accumulating cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(462792, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0101141', 'abnormal Keller explant', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(462793, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0101534', 'abnormal blastomere V2.1.1', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(462794, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0101022', 'abnormal blastomere V1.2', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(462795, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0101362', 'abnormal vegetal cortex', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(462796, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0141266', 'abnormal surface breathing', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(462797, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0100649', 'abnormal growth cone', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(462798, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0100383', 'abnormal amputated fin', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(462799, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0124716', 'absent cell', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(462800, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0126310', 'absent mitochondrial cloud', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(462801, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0101241', 'abnormal nucleate erythrocyte', 0.65, 3.6715585125471644, 1.5448343060521594, 'UPHENO:0086172', 'abnormal cell'),
(462802, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0107267', 'abnormal ventral side', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(462803, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0131082', 'abnormally increased number of alkali secreting cell', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(462804, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0100653', 'abnormal myoblast', 0.65, 3.6715585125471644, 1.5448343060521594, 'UPHENO:0086172', 'abnormal cell'),
(462805, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0102353', 'abnormal centromere morphology', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(462806, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0101452', 'abnormal blastomere V1.1.1', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(462807, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0100901', 'abnormal blastomere D1.2.2', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(462808, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0126404', 'abnormally localised circulating cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(462809, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0107285', 'abnormal flexural organ', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(462810, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0101406', 'abnormal cleavage furrow', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(462811, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0141743', 'abnormal chemical homeostasis within a tissue', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(462812, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0100722', 'abnormal barbel', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(462813, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0141263', 'abnormal visually guided collision avoidance behavior', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(462814, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0100626', 'abnormal primordial germ cell', 0.6190476190476191, 3.6715585125471644, 1.5076039119696991, 'UPHENO:0086172', 'abnormal cell'),
(462815, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0100935', 'abnormal skeleton', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(462816, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0130985', 'abnormally increased number of secondary oogonium', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(462817, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0101378', 'abnormal blastomere D1', 0.5652173913043478, 3.6715585125471644, 1.440565418328227, 'UPHENO:0086172', 'abnormal cell'),
(462818, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0131569', 'abnormally localised cortical actin cytoskeleton', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(462819, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0100515', 'abnormal somatic stem cell', 0.6190476190476191, 3.6715585125471644, 1.5076039119696991, 'UPHENO:0086172', 'abnormal cell'),
(462820, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0100727', 'abnormal odontogenic papilla', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(462821, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0102703', 'abnormal endoplasmic reticulum morphology', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(462822, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0125750', 'absent melanoblast', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(462823, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0127633', 'abnormally localised angioblast', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(462824, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0102896', 'abnormal mitotic spindle morphology', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(462825, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0127975', 'abnormally localised mitochondrial cloud', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(462826, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0131328', 'abnormally decreased number of paracrine cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(462827, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0100158', 'abnormal neuromere', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(462828, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0107287', 'abnormal afferent neuron', 0.48148148148148145, 3.6715585125471644, 1.3295816755533123, 'UPHENO:0086172', 'abnormal cell'),
(462829, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0101302', 'abnormal subcortical cytoplasm', 0.5652173913043478, 3.6715585125471644, 1.440565418328227, 'UPHENO:0086172', 'abnormal cell'),
(462830, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0100103', 'abnormal trunk', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(462831, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0131297', 'abnormally decreased number of melanoblast', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(462832, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0101387', 'abnormal melanophore', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(462833, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0102958', 'abnormal cementoblast morphology', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(462834, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0141718', 'abnormal posterior notochord', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(462835, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0131352', 'abnormally decreased number of barrier cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(462836, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0107398', 'abnormal apical junction complex morphology', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(462837, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0131002', 'abnormally increased number of secondary spermatogonium', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(462838, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0101311', 'abnormal bottle cell', 0.5652173913043478, 3.6715585125471644, 1.440565418328227, 'UPHENO:0086172', 'abnormal cell'),
(462839, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0100599', 'abnormal adult immune system', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(462840, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0107278', 'abnormal medial region', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(462841, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0102181', 'abnormal mitotic cell morphology', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(462842, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0103041', 'abnormal perivitelline space morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(462843, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0100307', 'abnormal blastomere', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(462844, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0127979', 'abnormally localised absorptive cell', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(462845, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0131523', 'absent actin filament', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(462846, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0131171', 'abnormally increased number of barrier epithelial cell', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(462847, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0115664', 'abnormally decreased mobility of migratory neural crest cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(462848, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0100274', 'abnormal sensory system', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(462849, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0101192', 'abnormal blastomere D2.1', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(462850, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0100417', 'abnormal dense regular connective tissue', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(462851, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0107261', 'abnormal dorsal-ventral axis', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(462852, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0100999', 'abnormal serous membrane', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(462853, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0141738', 'abnormal carbon dioxide homeostasis', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(462854, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0126783', 'abnormally localised exocrine cell', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(462855, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0102258', 'abnormal primordial germ cell morphology', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(462856, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0100060', 'abnormal regenerating tissue', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(462857, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0101278', 'abnormal pigment cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(462858, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0100444', 'abnormal cement gland', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(462859, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0100574', 'abnormal gastrula cell', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(462860, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0126314', 'absent absorptive cell', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(462861, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0100858', 'abnormal presumptive midbrain-hindbrain boundary', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(462862, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0102356', 'abnormal kinetochore morphology', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(462863, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0125351', 'absent secondary oogonium', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(462864, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0100004', 'abnormal cell', 0.6842105263157895, 3.6715585125471644, 1.584966555568007, 'UPHENO:0086172', 'abnormal cell'),
(462865, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0100993', 'abnormal ligament cell', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(462866, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0100477', 'abnormal pericyte', 0.65, 3.6715585125471644, 1.5448343060521594, 'UPHENO:0086172', 'abnormal cell'),
(462867, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0101133', 'abnormal motor neuron', 0.5, 3.6715585125471644, 1.3549093166236559, 'UPHENO:0086172', 'abnormal cell'),
(462868, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0101547', 'abnormal lampbrush chromosome', 0.6190476190476191, 3.6715585125471644, 1.5076039119696991, 'UPHENO:0086172', 'abnormal cell'),
(462869, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0100465', 'abnormal skeletal system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(462870, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0101174', 'abnormal articular system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(462871, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0127574', 'abnormally localised stage I oocyte', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(462872, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0131134', 'abnormally increased number of barrier cell', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(462873, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0102323', 'abnormal keratin accumulating cell morphology', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(462874, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0100605', 'abnormal prechordal plate', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(462875, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0142067', 'abnormally necrotic desmosome', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(462876, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0126082', 'absent perivitelline space', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(462877, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0101713', 'abnormal anatomical entity in vitro morphology', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(462878, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0100823', 'abnormal blood', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(462879, 'HP:0031551', 'Reduced cell surface marker level', 'XPO:0131735', 'abnormal spindle assembly', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(462880, 'HP:0010447', 'Anal fistula', 'XPO:0101321', 'abnormal duodenum', 0.46153846153846156, 8.518562886125473, 1.9828374640854927, 'UPHENO:0076783', 'abnormal intestine morphology'),
(462881, 'HP:0010447', 'Anal fistula', 'XPO:0107294', 'abnormal intestinal stem cell', 0.42857142857142855, 8.518562886125473, 1.9107099898944229, 'UPHENO:0076783', 'abnormal intestine morphology'),
(462882, 'HP:0010447', 'Anal fistula', 'XPO:0101537', 'abnormal internal coil of the small intestine', 0.46153846153846156, 8.518562886125473, 1.9828374640854927, 'UPHENO:0076783', 'abnormal intestine morphology'),
(462883, 'HP:0010447', 'Anal fistula', 'XPO:0101306', 'abnormal ileum', 0.46153846153846156, 8.518562886125473, 1.9828374640854927, 'UPHENO:0076783', 'abnormal intestine morphology'),
(462884, 'HP:0010447', 'Anal fistula', 'XPO:0115392', 'abnormally incomplete structure of alimentary system', 0.4090909090909091, 5.725717590856133, 1.5304701939081158, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(462885, 'HP:0010447', 'Anal fistula', 'XPO:0102473', 'abnormal large intestine morphology', 0.4067796610169492, 8.518562886125473, 1.8614988915306085, 'UPHENO:0076783', 'abnormal intestine morphology'),
(462886, 'HP:0010447', 'Anal fistula', 'XPO:0101784', 'abnormal alimentary system morphology', 0.4186046511627907, 5.725717590856133, 1.5481640787645816, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(462887, 'HP:0010447', 'Anal fistula', 'XPO:0102522', 'abnormal pharyngeal cavity morphology', 0.4186046511627907, 5.725717590856133, 1.5481640787645816, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(462888, 'HP:0010447', 'Anal fistula', 'XPO:0107288', 'abnormal larval alimentary system', 0.40540540540540543, 5.05060299610679, 1.4309233924911664, 'HP:0025031', 'Abnormality of the digestive system'),
(462889, 'HP:0010447', 'Anal fistula', 'XPO:0100152', 'abnormal alimentary system', 0.4166666666666667, 5.05060299610679, 1.45066119926208, 'HP:0025031', 'Abnormality of the digestive system'),
(462890, 'HP:0010447', 'Anal fistula', 'XPO:0101288', 'abnormal external coil of the small intestine', 0.46153846153846156, 8.518562886125473, 1.9828374640854927, 'UPHENO:0076783', 'abnormal intestine morphology'),
(462891, 'HP:0010447', 'Anal fistula', 'XPO:0100493', 'abnormal liver and biliary system', 0.40540540540540543, 5.05060299610679, 1.4309233924911664, 'HP:0025031', 'Abnormality of the digestive system'),
(462892, 'HP:0010447', 'Anal fistula', 'XPO:0100361', 'abnormal small intestine', 0.47058823529411764, 8.518562886125473, 2.002182677935196, 'UPHENO:0076783', 'abnormal intestine morphology'),
(462893, 'HP:0010447', 'Anal fistula', 'XPO:0101471', 'abnormal rectum', 0.43636363636363634, 8.518562886125473, 1.928001835471643, 'UPHENO:0076783', 'abnormal intestine morphology'),
(462894, 'HP:0010447', 'Anal fistula', 'XPO:0102788', 'abnormal typhlosole morphology', 0.41379310344827586, 8.518562886125473, 1.8774777158648677, 'UPHENO:0076783', 'abnormal intestine morphology'),
(462895, 'HP:0010447', 'Anal fistula', 'XPO:0115391', 'abnormally undifferentiated alimentary system', 0.40540540540540543, 5.05060299610679, 1.4309233924911664, 'HP:0025031', 'Abnormality of the digestive system'),
(462896, 'HP:0002630', 'Fat malabsorption', 'XPO:0101288', 'abnormal external coil of the small intestine', 0.4262295081967213, 10.103525386846629, 2.075191715646708, 'HP:0002244', 'Abnormal small intestine morphology'),
(462897, 'HP:0002630', 'Fat malabsorption', 'XPO:0101537', 'abnormal internal coil of the small intestine', 0.4262295081967213, 10.103525386846629, 2.075191715646708, 'HP:0002244', 'Abnormal small intestine morphology'),
(462898, 'HP:0002630', 'Fat malabsorption', 'XPO:0100361', 'abnormal small intestine', 0.43333333333333335, 10.103525386846629, 2.0924135189537, 'HP:0002244', 'Abnormal small intestine morphology'),
(462899, 'HP:0002630', 'Fat malabsorption', 'XPO:0101321', 'abnormal duodenum', 0.4262295081967213, 10.103525386846629, 2.075191715646708, 'HP:0002244', 'Abnormal small intestine morphology'),
(462900, 'HP:0002630', 'Fat malabsorption', 'XPO:0101306', 'abnormal ileum', 0.4262295081967213, 10.103525386846629, 2.075191715646708, 'HP:0002244', 'Abnormal small intestine morphology'),
(462901, 'HP:0011554', 'Double inlet atrioventricular connection', 'XPO:0101638', 'abnormal anatomical structure morphology', 0.4074074074074074, 2.485033483301678, 1.006191357919822, 'UPHENO:0076692', 'abnormal anatomical entity morphology'),
(462902, 'HP:0011554', 'Double inlet atrioventricular connection', 'XPO:0100054', 'abnormal blood vessel', 0.4117647058823529, 5.249153838287537, 1.4701755971154233, 'UPHENO:0080362', 'abnormal cardiovascular system'),
(462903, 'HP:0011554', 'Double inlet atrioventricular connection', 'XPO:0101919', 'abnormal heart primordium morphology', 0.425, 5.9590888072311134, 1.5914184688739863, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(462904, 'HP:0011554', 'Double inlet atrioventricular connection', 'XPO:0101995', 'abnormal cardiovascular system morphology', 0.4857142857142857, 5.9590888072311134, 1.7012979055745219, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(462905, 'HP:0011554', 'Double inlet atrioventricular connection', 'XPO:0102113', 'abnormal anatomical line morphology', 0.4074074074074074, 2.485033483301678, 1.006191357919822, 'UPHENO:0076692', 'abnormal anatomical entity morphology'),
(462906, 'HP:0011554', 'Double inlet atrioventricular connection', 'XPO:0139990', 'abnormally necrotic cardiovascular system', 0.4146341463414634, 5.9590888072311134, 1.57189112236161, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(462907, 'HP:0011554', 'Double inlet atrioventricular connection', 'XPO:0141328', 'edematous circulatory system', 0.4473684210526316, 5.9590888072311134, 1.6327608981732116, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(462908, 'HP:0011554', 'Double inlet atrioventricular connection', 'XPO:0102935', 'abnormal bulbous arteriosis morphology', 0.4473684210526316, 5.9590888072311134, 1.6327608981732116, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(462909, 'HP:0011554', 'Double inlet atrioventricular connection', 'XPO:0101770', 'abnormal trunk vasculature morphology', 0.40476190476190477, 5.9590888072311134, 1.5530653998657664, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(462910, 'HP:0011554', 'Double inlet atrioventricular connection', 'XPO:0102800', 'abnormal circulating cell morphology', 0.425, 5.9590888072311134, 1.5914184688739863, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(462911, 'HP:0011554', 'Double inlet atrioventricular connection', 'XPO:0101900', 'abnormal circulatory system morphology', 0.4857142857142857, 5.9590888072311134, 1.7012979055745219, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(462912, 'HP:0011554', 'Double inlet atrioventricular connection', 'XPO:0139811', 'abnormally necrotic circulatory system', 0.4146341463414634, 5.9590888072311134, 1.57189112236161, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(462913, 'HP:0011554', 'Double inlet atrioventricular connection', 'XPO:0101976', 'abnormal portion of organism substance morphology', 0.4074074074074074, 2.485033483301678, 1.006191357919822, 'UPHENO:0076692', 'abnormal anatomical entity morphology'),
(462914, 'HP:0011554', 'Double inlet atrioventricular connection', 'XPO:0101713', 'abnormal anatomical entity in vitro morphology', 0.4074074074074074, 2.485033483301678, 1.006191357919822, 'UPHENO:0076692', 'abnormal anatomical entity morphology'),
(462915, 'HP:0011554', 'Double inlet atrioventricular connection', 'XPO:0102532', 'abnormal angioblast morphology', 0.425, 5.9590888072311134, 1.5914184688739863, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(462916, 'HP:0012699', 'Anomaly of lower limb diaphyses', 'XPO:0101248', 'abnormal digit-joint region', 0.4642857142857143, 5.802924133159483, 1.6414063409496626, 'UPHENO:0076727', 'abnormal limb bone morphology'),
(462917, 'HP:0012699', 'Anomaly of lower limb diaphyses', 'XPO:0102880', 'abnormal digit-joint region morphology', 0.4918032786885246, 5.914846961127896, 1.7055618219295234, 'UPHENO:0084763', 'abnormal anatomical entity morphology in the appendage girdle complex'),
(462918, 'HP:0012699', 'Anomaly of lower limb diaphyses', 'XPO:0103632', 'abnormally increased number of digit', 0.421875, 5.802924133159483, 1.564643287997829, 'UPHENO:0076727', 'abnormal limb bone morphology'),
(462919, 'HP:0012699', 'Anomaly of lower limb diaphyses', 'XPO:0139808', 'abnormally necrotic pelvic girdle', 0.4032258064516129, 7.61213700143767, 1.7519731964915635, 'UPHENO:0079871', 'abnormal anatomical entity morphology in the skeleton of pelvic complex'),
(462920, 'HP:0012699', 'Anomaly of lower limb diaphyses', 'XPO:0101810', 'abnormal digit morphology', 0.4918032786885246, 5.914846961127896, 1.7055618219295234, 'UPHENO:0084763', 'abnormal anatomical entity morphology in the appendage girdle complex'),
(462921, 'HP:0012699', 'Anomaly of lower limb diaphyses', 'XPO:0128497', 'decreased size of the digit-joint region', 0.44776119402985076, 5.914846961127896, 1.6274025125390648, 'UPHENO:0084763', 'abnormal anatomical entity morphology in the appendage girdle complex'),
(462922, 'HP:0012699', 'Anomaly of lower limb diaphyses', 'XPO:0141569', 'abnormal digit-joint region morphology in the regenerating hindlimb', 0.44776119402985076, 5.914846961127896, 1.6274025125390648, 'UPHENO:0084763', 'abnormal anatomical entity morphology in the appendage girdle complex'),
(462923, 'HP:0012699', 'Anomaly of lower limb diaphyses', 'XPO:0128213', 'decreased size of the digit', 0.42857142857142855, 5.914846961127896, 1.5921477355798221, 'UPHENO:0084763', 'abnormal anatomical entity morphology in the appendage girdle complex'),
(462924, 'HP:0012699', 'Anomaly of lower limb diaphyses', 'XPO:0101755', 'abnormal pelvic girdle morphology', 0.44642857142857145, 7.61213700143767, 1.843441197074208, 'UPHENO:0079871', 'abnormal anatomical entity morphology in the skeleton of pelvic complex'),
(462925, 'HP:0012699', 'Anomaly of lower limb diaphyses', 'XPO:0103008', 'abnormal iliac process morphology', 0.4050632911392405, 7.61213700143767, 1.7559604968236422, 'UPHENO:0079871', 'abnormal anatomical entity morphology in the skeleton of pelvic complex'),
(462926, 'HP:0012699', 'Anomaly of lower limb diaphyses', 'XPO:0129977', 'increased size of the digit-joint region', 0.44776119402985076, 5.914846961127896, 1.6274025125390648, 'UPHENO:0084763', 'abnormal anatomical entity morphology in the appendage girdle complex'),
(462927, 'HP:0012699', 'Anomaly of lower limb diaphyses', 'XPO:0125443', 'absent digit-joint region', 0.4153846153846154, 5.802924133159483, 1.5525609196287773, 'UPHENO:0076727', 'abnormal limb bone morphology'),
(462928, 'HP:0012699', 'Anomaly of lower limb diaphyses', 'XPO:0141568', 'abnormal digit-joint region morphology in the regenerating forelimb', 0.44776119402985076, 5.914846961127896, 1.6274025125390648, 'UPHENO:0084763', 'abnormal anatomical entity morphology in the appendage girdle complex'),
(462929, 'HP:0012699', 'Anomaly of lower limb diaphyses', 'XPO:0141208', 'abnormally necrotic digit-joint region', 0.46153846153846156, 5.914846961127896, 1.652249789430888, 'UPHENO:0084763', 'abnormal anatomical entity morphology in the appendage girdle complex'),
(462930, 'HP:0012699', 'Anomaly of lower limb diaphyses', 'XPO:0124986', 'absent digit', 0.4090909090909091, 5.802924133159483, 1.5407542013636661, 'UPHENO:0076727', 'abnormal limb bone morphology'),
(462931, 'HP:0012699', 'Anomaly of lower limb diaphyses', 'XPO:0100178', 'abnormal digit', 0.49056603773584906, 5.802924133159483, 1.6872218287130427, 'UPHENO:0076727', 'abnormal limb bone morphology'),
(462932, 'HP:0012699', 'Anomaly of lower limb diaphyses', 'XPO:0126603', 'abnormally localised digit', 0.421875, 5.802924133159483, 1.564643287997829, 'UPHENO:0076727', 'abnormal limb bone morphology'),
(462933, 'HP:0012699', 'Anomaly of lower limb diaphyses', 'XPO:0139962', 'abnormally necrotic digit', 0.4411764705882353, 5.914846961127896, 1.6153919977454247, 'UPHENO:0084763', 'abnormal anatomical entity morphology in the appendage girdle complex'),
(462934, 'HP:0012699', 'Anomaly of lower limb diaphyses', 'XPO:0101859', 'abnormal hindlimb skeleton morphology', 0.4375, 7.61213700143767, 1.8249136796377468, 'UPHENO:0079871', 'abnormal anatomical entity morphology in the skeleton of pelvic complex'),
(462935, 'HP:0012699', 'Anomaly of lower limb diaphyses', 'XPO:0129693', 'increased size of the digit', 0.42857142857142855, 5.914846961127896, 1.5921477355798221, 'UPHENO:0084763', 'abnormal anatomical entity morphology in the appendage girdle complex'),
(462936, 'HP:0012699', 'Anomaly of lower limb diaphyses', 'XPO:0127078', 'abnormally localised digit-joint region', 0.42857142857142855, 5.802924133159483, 1.5770122021213973, 'UPHENO:0076727', 'abnormal limb bone morphology'),
(462937, 'HP:0009820', 'Lower limb peromelia', 'XPO:0103292', 'absent hindlimb digit 4', 0.41904761904761906, 10.299160507394836, 2.0774596720064324, 'HP:0006494', 'Aplasia/Hypoplasia involving bones of the feet'),
(462938, 'HP:0009820', 'Lower limb peromelia', 'XPO:0103838', 'abnormally decreased number of hindlimb digit in the regenerating hindlimb', 0.45045045045045046, 12.354068848497226, 2.3590031533894678, 'UPHENO:0035060', 'abnormally decreased number of anatomical entity in the limb'),
(462939, 'HP:0009820', 'Lower limb peromelia', 'XPO:0103289', 'absent hindlimb digit', 0.43137254901960786, 10.299160507394836, 2.107789154739389, 'HP:0006494', 'Aplasia/Hypoplasia involving bones of the feet'),
(462940, 'HP:0009820', 'Lower limb peromelia', 'XPO:0103293', 'absent hindlimb digit 5', 0.41904761904761906, 10.299160507394836, 2.0774596720064324, 'HP:0006494', 'Aplasia/Hypoplasia involving bones of the feet'),
(462941, 'HP:0009820', 'Lower limb peromelia', 'XPO:0103290', 'absent hindlimb digit 2', 0.41904761904761906, 10.299160507394836, 2.0774596720064324, 'HP:0006494', 'Aplasia/Hypoplasia involving bones of the feet'),
(462942, 'HP:0009820', 'Lower limb peromelia', 'XPO:0103291', 'absent hindlimb digit 3', 0.41904761904761906, 10.299160507394836, 2.0774596720064324, 'HP:0006494', 'Aplasia/Hypoplasia involving bones of the feet'),
(462943, 'HP:0009820', 'Lower limb peromelia', 'XPO:0103908', 'absent hindlimb digit 1', 0.41904761904761906, 10.299160507394836, 2.0774596720064324, 'HP:0006494', 'Aplasia/Hypoplasia involving bones of the feet'),
(462944, 'HP:0009820', 'Lower limb peromelia', 'XPO:0103589', 'abnormally decreased number of hindlimb digit', 0.47619047619047616, 12.354068848497226, 2.4254669504769226, 'UPHENO:0035060', 'abnormally decreased number of anatomical entity in the limb'),
(462945, 'HP:0009820', 'Lower limb peromelia', 'XPO:0103833', 'abnormally decreased number of digit-joint region in the regenerating forelimb', 0.44155844155844154, 12.354068848497226, 2.335603431160377, 'UPHENO:0035060', 'abnormally decreased number of anatomical entity in the limb'),
(462946, 'HP:0009820', 'Lower limb peromelia', 'XPO:0103839', 'abnormally decreased number of digit-joint region in the regenerating hindlimb', 0.44155844155844154, 12.354068848497226, 2.335603431160377, 'UPHENO:0035060', 'abnormally decreased number of anatomical entity in the limb'),
(462947, 'HP:0010156', 'Pseudoepiphysis of the 1st metatarsal', 'XPO:0102180', 'abnormal hindlimb digit 3 morphology', 0.40186915887850466, 7.639349617137506, 1.752146970153439, 'UPHENO:0088132', 'abnormal pedal digit morphology'),
(462948, 'HP:0010156', 'Pseudoepiphysis of the 1st metatarsal', 'XPO:0102876', 'abnormal hindlimb digit 4 morphology', 0.40186915887850466, 7.639349617137506, 1.752146970153439, 'UPHENO:0088132', 'abnormal pedal digit morphology'),
(462949, 'HP:0010156', 'Pseudoepiphysis of the 1st metatarsal', 'XPO:0102051', 'abnormal hindlimb digit 2 morphology', 0.40186915887850466, 7.639349617137506, 1.752146970153439, 'HP:0001780', 'Abnormal toe morphology'),
(462950, 'HP:0010156', 'Pseudoepiphysis of the 1st metatarsal', 'XPO:0101809', 'abnormal hindlimb digit morphology', 0.4095238095238095, 7.639349617137506, 1.7687553696015759, 'UPHENO:0088132', 'abnormal pedal digit morphology'),
(462951, 'HP:0010156', 'Pseudoepiphysis of the 1st metatarsal', 'XPO:0102948', 'abnormal hindlimb digit 5 morphology', 0.40186915887850466, 7.639349617137506, 1.752146970153439, 'UPHENO:0088132', 'abnormal pedal digit morphology'),
(462952, 'HP:0010156', 'Pseudoepiphysis of the 1st metatarsal', 'XPO:0102566', 'abnormal claw primordium morphology', 0.41346153846153844, 7.639349617137506, 1.7772386574535335, 'UPHENO:0088132', 'abnormal pedal digit morphology'),
(462953, 'HP:0010156', 'Pseudoepiphysis of the 1st metatarsal', 'XPO:0101872', 'abnormal hindlimb digit 1 morphology', 0.40186915887850466, 7.639349617137506, 1.752146970153439, 'HP:0001780', 'Abnormal toe morphology'),
(462954, 'HP:0006353', 'Hypoplasia of the tooth germ', 'XPO:0101659', 'abnormal lower jaw morphology', 0.4634146341463415, 7.312692920701687, 1.8408717811057655, 'UPHENO:0076800', 'abnormal mouth morphology'),
(462955, 'HP:0006353', 'Hypoplasia of the tooth germ', 'XPO:0102861', 'abnormal cementum morphology', 0.5168539325842697, 11.200822588201543, 2.406073399314885, 'HP:0011061', 'Abnormality of dental structure'),
(462956, 'HP:0006353', 'Hypoplasia of the tooth germ', 'XPO:0102960', 'abnormal oral epithelium morphology', 0.4074074074074074, 7.312692920701687, 1.7260490329042149, 'UPHENO:0076800', 'abnormal mouth morphology'),
(462957, 'HP:0006353', 'Hypoplasia of the tooth germ', 'XPO:0103096', 'abnormal oral cavity morphology', 0.4861111111111111, 7.884497199543557, 1.9577389239177327, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(462958, 'HP:0006353', 'Hypoplasia of the tooth germ', 'XPO:0128510', 'decreased size of the cementum', 0.5104166666666666, 11.200822588201543, 2.3910429794118166, 'HP:0011061', 'Abnormality of dental structure'),
(462959, 'HP:0006353', 'Hypoplasia of the tooth germ', 'XPO:0131573', 'decreased size of the roof of mouth', 0.45569620253164556, 7.312692920701687, 1.8254770319683034, 'UPHENO:0076800', 'abnormal mouth morphology'),
(462960, 'HP:0006353', 'Hypoplasia of the tooth germ', 'XPO:0129449', 'decreased size of the dentine', 0.494949494949495, 11.200822588201543, 2.354536362651732, 'HP:0011061', 'Abnormality of dental structure'),
(462961, 'HP:0006353', 'Hypoplasia of the tooth germ', 'XPO:0103352', 'decreased size of the mouth', 0.48717948717948717, 7.884497199543557, 1.9598891046030469, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(462962, 'HP:0006353', 'Hypoplasia of the tooth germ', 'XPO:0127750', 'abnormally localised tongue', 0.4342105263157895, 7.884497199543557, 1.8502788110847448, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(462963, 'HP:0006353', 'Hypoplasia of the tooth germ', 'XPO:0102279', 'abnormal mouth morphology', 0.4583333333333333, 7.312692920701687, 1.830751463740579, 'UPHENO:0076800', 'abnormal mouth morphology'),
(462964, 'HP:0006353', 'Hypoplasia of the tooth germ', 'XPO:0141006', 'abnormally necrotic cementum', 0.4742268041237113, 11.200822588201543, 2.304719136805935, 'HP:0011061', 'Abnormality of dental structure'),
(462965, 'HP:0006353', 'Hypoplasia of the tooth germ', 'XPO:0101816', 'abnormal tooth morphology', 0.5555555555555556, 9.872199840740173, 2.34191277956244, 'HP:0006482', 'Abnormal dental morphology'),
(462966, 'HP:0006353', 'Hypoplasia of the tooth germ', 'XPO:0103828', 'decreased width of the mouth', 0.4578313253012048, 7.884497199543557, 1.8999394206660023, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(462967, 'HP:0006353', 'Hypoplasia of the tooth germ', 'XPO:0140789', 'abnormally necrotic roof of mouth', 0.4125, 7.312692920701687, 1.7368033365322182, 'UPHENO:0076800', 'abnormal mouth morphology'),
(462968, 'HP:0006353', 'Hypoplasia of the tooth germ', 'XPO:0140626', 'abnormally necrotic tongue', 0.45454545454545453, 7.884497199543557, 1.8931091789510952, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(462969, 'HP:0006353', 'Hypoplasia of the tooth germ', 'XPO:0102890', 'abnormal dentine morphology', 0.5054945054945055, 11.200822588201543, 2.379486136827577, 'HP:0011061', 'Abnormality of dental structure'),
(462970, 'HP:0006353', 'Hypoplasia of the tooth germ', 'XPO:0130628', 'increased size of the oral cavity', 0.47368421052631576, 7.884497199543557, 1.932553189788767, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(462971, 'HP:0006353', 'Hypoplasia of the tooth germ', 'XPO:0141311', 'abnormal roof of mouth morphology', 0.44, 7.312692920701687, 1.7937627728071353, 'UPHENO:0076800', 'abnormal mouth morphology'),
(462972, 'HP:0006353', 'Hypoplasia of the tooth germ', 'XPO:0128105', 'decreased size of the tongue', 0.48148148148148145, 7.884497199543557, 1.9483940546955134, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(462973, 'HP:0006353', 'Hypoplasia of the tooth germ', 'XPO:0139736', 'abnormally necrotic tooth', 0.5056179775280899, 9.872199840740173, 2.2341803233463895, 'HP:0006482', 'Abnormal dental morphology'),
(462974, 'HP:0006353', 'Hypoplasia of the tooth germ', 'XPO:0115558', 'abnormally incomplete structure of mouth', 0.4520547945205479, 7.312692920701687, 1.8181688303509294, 'UPHENO:0076800', 'abnormal mouth morphology'),
(462975, 'HP:0006353', 'Hypoplasia of the tooth germ', 'XPO:0140639', 'abnormally necrotic upper jaw', 0.42696629213483145, 7.312692920701687, 1.7669955806035935, 'UPHENO:0076800', 'abnormal mouth morphology'),
(462976, 'HP:0006353', 'Hypoplasia of the tooth germ', 'XPO:0129990', 'increased size of the cementum', 0.47959183673469385, 11.200822588201543, 2.3177193699874508, 'HP:0011061', 'Abnormality of dental structure'),
(462977, 'HP:0006353', 'Hypoplasia of the tooth germ', 'XPO:0128989', 'decreased size of the tooth', 0.5333333333333333, 9.872199840740173, 2.2945965328124154, 'HP:0006482', 'Abnormal dental morphology'),
(462978, 'HP:0006353', 'Hypoplasia of the tooth germ', 'XPO:0141830', 'increased width of mouth', 0.4235294117647059, 7.884497199543557, 1.8273796707261338, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(462979, 'HP:0006353', 'Hypoplasia of the tooth germ', 'XPO:0130923', 'increased size of the dentine', 0.46534653465346537, 11.200822588201543, 2.283038321335813, 'HP:0011061', 'Abnormality of dental structure'),
(462980, 'HP:0006353', 'Hypoplasia of the tooth germ', 'XPO:0103138', 'abnormal upper jaw morphology', 0.4523809523809524, 7.312692920701687, 1.8188246171460507, 'UPHENO:0076800', 'abnormal mouth morphology'),
(462981, 'HP:0006353', 'Hypoplasia of the tooth germ', 'XPO:0129225', 'decreased size of the upper jaw', 0.4659090909090909, 7.312692920701687, 1.8458196311615789, 'UPHENO:0076800', 'abnormal mouth morphology'),
(462982, 'HP:0006353', 'Hypoplasia of the tooth germ', 'XPO:0103735', 'increased size of the mouth', 0.45, 7.884497199543557, 1.8836198501275678, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(462983, 'HP:0006353', 'Hypoplasia of the tooth germ', 'XPO:0101567', 'abnormal tongue', 0.48484848484848486, 7.884497199543557, 1.9551947527013303, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(462984, 'HP:0006353', 'Hypoplasia of the tooth germ', 'XPO:0103199', 'abnormal tongue morphology', 0.4861111111111111, 7.884497199543557, 1.9577389239177327, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(462985, 'HP:0006353', 'Hypoplasia of the tooth germ', 'XPO:0128653', 'decreased size of the oral epithelium', 0.41379310344827586, 7.312692920701687, 1.7395234687181969, 'UPHENO:0076800', 'abnormal mouth morphology'),
(462986, 'HP:0006353', 'Hypoplasia of the tooth germ', 'XPO:0129152', 'decreased size of the oral cavity', 0.5135135135135135, 7.884497199543557, 2.0121619863284046, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(462987, 'HP:0006353', 'Hypoplasia of the tooth germ', 'XPO:0140890', 'abnormally necrotic dentine', 0.46, 11.200822588201543, 2.269885105147992, 'HP:0011061', 'Abnormality of dental structure'),
(462988, 'HP:0006353', 'Hypoplasia of the tooth germ', 'XPO:0130358', 'increased size of the lower jaw', 0.4431818181818182, 7.312692920701687, 1.80023680231293, 'UPHENO:0076800', 'abnormal mouth morphology'),
(462989, 'HP:0006353', 'Hypoplasia of the tooth germ', 'XPO:0115393', 'abnormally decreased volume of oral cavity', 0.5, 7.884497199543557, 1.9855096574360394, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(462990, 'HP:0006353', 'Hypoplasia of the tooth germ', 'XPO:0126089', 'absent tongue', 0.4230769230769231, 7.884497199543557, 1.8264032455050843, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(462991, 'HP:0006353', 'Hypoplasia of the tooth germ', 'XPO:0130466', 'increased size of the tooth', 0.5, 9.872199840740173, 2.2217335394619413, 'HP:0006482', 'Abnormal dental morphology'),
(462992, 'HP:0006353', 'Hypoplasia of the tooth germ', 'XPO:0128880', 'decreased size of the lower jaw', 0.47674418604651164, 7.312692920701687, 1.86715929537038, 'UPHENO:0076800', 'abnormal mouth morphology'),
(462993, 'HP:0006353', 'Hypoplasia of the tooth germ', 'XPO:0129585', 'increased size of the tongue', 0.42045454545454547, 7.884497199543557, 1.8207341063899811, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(462994, 'HP:0006353', 'Hypoplasia of the tooth germ', 'XPO:0140897', 'abnormally necrotic lower jaw', 0.4367816091954023, 7.312692920701687, 1.7871904715099365, 'UPHENO:0076800', 'abnormal mouth morphology'),
(462995, 'HP:0006353', 'Hypoplasia of the tooth germ', 'XPO:0131611', 'increased size of the roof of mouth', 0.41975308641975306, 7.312692920701687, 1.752006114003148, 'UPHENO:0076800', 'abnormal mouth morphology'),
(462996, 'HP:0006353', 'Hypoplasia of the tooth germ', 'XPO:0130701', 'increased size of the upper jaw', 0.43333333333333335, 7.312692920701687, 1.7801217932969449, 'UPHENO:0076800', 'abnormal mouth morphology'),
(462997, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0100386', 'abnormal limb', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(462998, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0100643', 'abnormal thoracic region', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(462999, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0101240', 'abnormal ciliated non-epidermal cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(463000, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0100225', 'abnormal endocrine system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(463001, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0100894', 'abnormal nucleus', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(463002, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0100437', 'abnormal proepicardium', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(463003, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0100344', 'abnormal portion of organism substance', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463004, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0101740', 'abnormal cell part morphology', 0.41379310344827586, 2.13901709234296, 0.9408031255100615, 'UPHENO:0075696', 'abnormal anatomical entity'),
(463005, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0127710', 'abnormally localised adult immune system', 0.42424242424242425, 5.64885357140806, 1.548057923116778, 'HP:0002715', 'Abnormality of the immune system'),
(463006, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0100969', 'abnormal disaggregated/reaggregated ectoderm treated with activin', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463007, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0100533', 'abnormal melanoblast', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(463008, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0100888', 'abnormal microtubule', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(463009, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0101638', 'abnormal anatomical structure morphology', 0.43478260869565216, 2.13901709234296, 0.9643689291207286, 'UPHENO:0075696', 'abnormal anatomical entity'),
(463010, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0131666', 'abnormal adherens junction', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(463011, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0101228', 'abnormal mesenchymal stem cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(463012, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0101373', 'abnormal oxygen accumulating cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(463013, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0100581', 'abnormal immune system', 0.5652173913043478, 5.64885357140806, 1.786849260427838, 'HP:0002715', 'Abnormality of the immune system'),
(463014, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0101311', 'abnormal bottle cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(463015, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0100423', 'abnormal process', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463016, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0100791', 'abnormal multiciliated cell precursor', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(463017, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0126909', 'abnormally localised lymphocyte', 0.4117647058823529, 5.64885357140806, 1.525122463739656, 'HP:0002715', 'Abnormality of the immune system'),
(463018, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0141263', 'abnormal visually guided collision avoidance behavior', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(463019, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0100704', 'abnormal Merkel cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(463020, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0100108', 'abnormal cell part', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(463021, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0141315', 'abnormal anatomical region', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463022, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0127101', 'abnormally localised portion of organism substance', 0.4166666666666667, 2.13901709234296, 0.944064151321067, 'UPHENO:0075696', 'abnormal anatomical entity'),
(463023, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0126559', 'abnormally localised lymphatic system', 0.45161290322580644, 5.64885357140806, 1.5972148137558264, 'HP:0002715', 'Abnormality of the immune system'),
(463024, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0100152', 'abnormal alimentary system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(463025, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0100587', 'abnormal vestibuloauditory system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(463026, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0100802', 'abnormal exocrine cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(463027, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0100688', 'abnormal adipose tissue', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(463028, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0100762', 'abnormal intersomitic region', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463029, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0101302', 'abnormal subcortical cytoplasm', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(463030, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0100081', 'abnormal anatomical entity in vitro', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463031, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0100599', 'abnormal adult immune system', 0.5416666666666666, 5.64885357140806, 1.7492271677837328, 'HP:0002715', 'Abnormality of the immune system'),
(463032, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0141738', 'abnormal carbon dioxide homeostasis', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(463033, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0100372', 'abnormal hematological system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(463034, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0100887', 'abnormal right-dorsal blastomere', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(463035, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0101141', 'abnormal Keller explant', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463036, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0100784', 'abnormal left blastomere', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(463037, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0107284', 'abnormal migrating myoblast', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(463038, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0102853', 'abnormal larval immune system morphology', 0.42424242424242425, 5.64885357140806, 1.548057923116778, 'HP:0002715', 'Abnormality of the immune system'),
(463039, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0101547', 'abnormal lampbrush chromosome', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(463040, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0125107', 'absent immune system', 0.4375, 5.64885357140806, 1.5720602525002108, 'HP:0002715', 'Abnormality of the immune system'),
(463041, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0100277', 'abnormal blastocoel', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463042, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0126677', 'abnormally localised dorsal lymph space', 0.45161290322580644, 5.64885357140806, 1.5972148137558264, 'HP:0002715', 'Abnormality of the immune system'),
(463043, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0107271', 'abnormal apical region', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463044, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0101463', 'abnormal right-ventral blastomere', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(463045, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0100317', 'abnormal respiratory system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(463046, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0100852', 'abnormal interdigital region', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(463047, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0101411', 'abnormal marginal zone (sensu neural)', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463048, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0101535', 'abnormal absorptive cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(463049, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0126050', 'absent adult immune system', 0.4117647058823529, 5.64885357140806, 1.525122463739656, 'HP:0002715', 'Abnormality of the immune system'),
(463050, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0125106', 'absent larval immune system', 0.4117647058823529, 5.64885357140806, 1.525122463739656, 'HP:0002715', 'Abnormality of the immune system'),
(463051, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0100273', 'abnormal visual system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(463052, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0101061', 'abnormal plasma membrane', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(463053, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0141770', 'abnormal urate homeostasis', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(463054, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0101237', 'abnormal mucus secreting cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(463055, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0131685', 'abnormal cortical actin cytoskeleton', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(463056, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0100031', 'abnormal central nervous system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(463057, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0107258', 'abnormal anatomical axis', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463058, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0100515', 'abnormal somatic stem cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(463059, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0100172', 'abnormal stem cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(463060, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0100547', 'abnormal blastomere V2', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(463061, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0107260', 'abnormal anterior-posterior axis', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463062, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0131687', 'abnormal astral microtubule', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(463063, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0100862', 'abnormal blastomere V1', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(463064, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0101480', 'abnormal stage V oocyte', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(463065, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0107270', 'abnormal proximal-distal axis', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463066, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0100477', 'abnormal pericyte', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(463067, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0101409', 'abnormal perivitelline space', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(463068, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0100449', 'abnormal lymphocyte', 0.48148148148148145, 5.64885357140806, 1.6491871895674883, 'HP:0002715', 'Abnormality of the immune system'),
(463069, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0107253', 'abnormal enteric nervous system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(463070, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0131669', 'abnormal Roux spot', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(463071, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0101575', 'abnormal vitelline membrane', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(463072, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0100715', 'abnormal ciliated cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(463073, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0100674', 'abnormal secondary oogonium', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(463074, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0101497', 'abnormal ciliary axoneme', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(463075, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0100084', 'abnormal anatomical group', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463076, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0141264', 'abnormal schooling behavior', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(463077, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0107261', 'abnormal dorsal-ventral axis', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463078, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0101347', 'abnormal hindlimb region', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463079, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0100205', 'abnormal limb segment', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(463080, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0101435', 'abnormal paracrine cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(463081, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0100218', 'abnormal epithelial cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(463082, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0101451', 'abnormal dorsal lymph space', 0.52, 5.64885357140806, 1.713885602113569, 'HP:0002715', 'Abnormality of the immune system'),
(463083, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0100307', 'abnormal blastomere', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(463084, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0100392', 'abnormal cilium', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(463085, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0126624', 'abnormally localised anatomical line', 0.4166666666666667, 2.13901709234296, 0.944064151321067, 'UPHENO:0075696', 'abnormal anatomical entity'),
(463086, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0100642', 'abnormal gustatory system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(463087, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0107263', 'abnormal anatomical side', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463088, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0100574', 'abnormal gastrula cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(463089, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0100754', 'abnormal electrically active cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(463090, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0101221', 'abnormal larval immune system', 0.5416666666666666, 5.64885357140806, 1.7492271677837328, 'HP:0002715', 'Abnormality of the immune system'),
(463091, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0141748', 'abnormal gas homeostasis', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(463092, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0100917', 'abnormal stage III oocyte', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(463093, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0115508', 'abnormally peramorphic growth of whole organism', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463094, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0141497', 'abnormal lymphoblast', 0.48148148148148145, 5.64885357140806, 1.6491871895674883, 'HP:0002715', 'Abnormality of the immune system'),
(463095, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0141472', 'abnormally localised lymphoblast', 0.4117647058823529, 5.64885357140806, 1.525122463739656, 'HP:0002715', 'Abnormality of the immune system'),
(463096, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0100551', 'abnormal oocyte cortex', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(463097, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0100481', 'abnormal anatomical line', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463098, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0100842', 'abnormal left-dorsal blastomere', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(463099, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0101113', 'abnormal stage IV oocyte', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(463100, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0115509', 'abnormally semi-viable whole organism', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463101, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0100026', 'abnormal germ cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(463102, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0101029', 'abnormal right spleen primordium', 0.48148148148148145, 5.64885357140806, 1.6491871895674883, 'HP:0002715', 'Abnormality of the immune system'),
(463103, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0102213', 'abnormal immune system morphology', 0.45161290322580644, 5.64885357140806, 1.5972148137558264, 'HP:0002715', 'Abnormality of the immune system'),
(463104, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0101864', 'abnormal lymphatic system morphology', 0.45161290322580644, 5.64885357140806, 1.5972148137558264, 'HP:0002715', 'Abnormality of the immune system'),
(463105, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0100032', 'abnormal nervous system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(463106, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0141776', 'abnormal metabolic process', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(463107, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0107273', 'abnormal basal region', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463108, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0107262', 'abnormal left-right axis', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463109, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0100585', 'abnormal elastica externa', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(463110, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0102113', 'abnormal anatomical line morphology', 0.43478260869565216, 2.13901709234296, 0.9643689291207286, 'UPHENO:0075696', 'abnormal anatomical entity'),
(463111, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0100337', 'abnormal zygote', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(463112, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0100004', 'abnormal cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(463113, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0100724', 'abnormal kinetochore', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(463114, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0100549', 'abnormal mitotic cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(463115, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0100009', 'abnormal multi-tissue structure', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463116, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0100814', 'abnormal natural killer cell', 0.4482758620689655, 5.64885357140806, 1.5913028324062968, 'HP:0002715', 'Abnormality of the immune system'),
(463117, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0141841', 'abnormality of whole organism mass', 0.4444444444444444, 2.13901709234296, 0.9750252628847818, 'UPHENO:0075696', 'abnormal anatomical entity'),
(463118, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0101472', 'abnormal zygote cortex', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(463119, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0125007', 'absent anatomical line', 0.4166666666666667, 2.13901709234296, 0.944064151321067, 'UPHENO:0075696', 'abnormal anatomical entity'),
(463120, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0107259', 'abnormal animal-vegetal axis', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463121, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0101297', 'abnormal barrier cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(463122, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0102377', 'abnormal anterior lymph sac morphology', 0.4117647058823529, 5.64885357140806, 1.525122463739656, 'HP:0002715', 'Abnormality of the immune system'),
(463123, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0107339', 'abnormal yolk platelet', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(463124, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0142057', 'abnormal desmosome', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(463125, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0141265', 'abnormal escape behavior', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(463126, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0100823', 'abnormal blood', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(463127, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0101333', 'abnormal barrier epithelial cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(463128, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0101071', 'abnormal endoplasmic reticulum', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(463129, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0101389', 'abnormal wedge region', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(463130, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0100503', 'abnormal blastomere D2', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(463131, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0100501', 'abnormal urogenital system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(463132, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0100295', 'abnormal extracellular matrix', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463133, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0101072', 'abnormal mitochondrial cloud', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(463134, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0100006', 'abnormal anatomical structure', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463135, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0115512', 'abnormally semi-erect whole organism', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463136, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0101083', 'abnormal T cell', 0.4642857142857143, 5.64885357140806, 1.6194696710023933, 'HP:0002715', 'Abnormality of the immune system'),
(463137, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0107312', 'abnormal filopodium', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(463138, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0141272', 'absent surface breathing', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(463139, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0124945', 'absent lymphatic system', 0.42424242424242425, 5.64885357140806, 1.548057923116778, 'HP:0002715', 'Abnormality of the immune system'),
(463140, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0101136', 'abnormal ooplasm', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(463141, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0141499', 'abnormal tadpole', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463142, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0100202', 'abnormal embryo', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463143, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0100989', 'abnormal right blastomere', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(463144, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0100028', 'abnormal anatomical cluster', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463145, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0141743', 'abnormal chemical homeostasis within a tissue', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(463146, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0100417', 'abnormal dense regular connective tissue', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(463147, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0100176', 'abnormal stage VI oocyte', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(463148, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0101326', 'abnormal cementoblast', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(463149, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0100010', 'abnormal multicellular anatomical structure', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463150, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0100907', 'abnormal cytoplasm', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(463151, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0101498', 'abnormal stage II oocyte', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(463152, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0101220', 'abnormal centriole', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(463153, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0101004', 'abnormal acid secreting cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(463154, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0131723', 'abnormal pathway-restricted SMAD protein phosphorylation', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(463155, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0141622', 'metaplastic right lymph heart', 0.45161290322580644, 5.64885357140806, 1.5972148137558264, 'HP:0002715', 'Abnormality of the immune system'),
(463156, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0100285', 'abnormal progenitor cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(463157, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0141784', 'abnormal cellular hormone metabolic process', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(463158, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0101461', 'abnormal sperm entry point', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(463159, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0141267', 'abnormal resting posture', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(463160, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0101110', 'abnormal cell-free extract', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463161, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0126321', 'abnormally localised anatomical structure', 0.4166666666666667, 2.13901709234296, 0.944064151321067, 'UPHENO:0075696', 'abnormal anatomical entity'),
(463162, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0100465', 'abnormal skeletal system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(463163, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0101283', 'abnormal left-ventral blastomere', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(463164, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0101378', 'abnormal blastomere D1', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(463165, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0100691', 'abnormal keratin accumulating cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(463166, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:00000000', 'Xenopus phenotype', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(463167, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0124719', 'absent anatomical structure', 0.4166666666666667, 2.13901709234296, 0.944064151321067, 'UPHENO:0075696', 'abnormal anatomical entity'),
(463168, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0101518', 'abnormal B cell', 0.4642857142857143, 5.64885357140806, 1.6194696710023933, 'HP:0002715', 'Abnormality of the immune system'),
(463169, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0100540', 'abnormal left lymph heart', 0.4642857142857143, 5.64885357140806, 1.6194696710023933, 'HP:0002715', 'Abnormality of the immune system'),
(463170, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0131675', 'abnormal spindle microtubule', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(463171, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0100721', 'abnormal centromere', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(463172, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0107278', 'abnormal medial region', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463173, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0101976', 'abnormal portion of organism substance morphology', 0.43478260869565216, 2.13901709234296, 0.9643689291207286, 'UPHENO:0075696', 'abnormal anatomical entity'),
(463174, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0141628', 'metaplastic thymus', 0.4117647058823529, 5.64885357140806, 1.525122463739656, 'HP:0002715', 'Abnormality of the immune system'),
(463175, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0101157', 'abnormal female organism', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463176, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0102231', 'abnormal adult immune system morphology', 0.42424242424242425, 5.64885357140806, 1.548057923116778, 'HP:0002715', 'Abnormality of the immune system'),
(463177, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0100638', 'abnormal polar body', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(463178, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0101109', 'abnormal egg cell-free extract', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463179, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0131725', 'abnormal phosphorylation of RNA polymerase II C-terminal domain', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(463180, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0100546', 'abnormal whole organism', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463181, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0100308', 'abnormal early embryonic cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(463182, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0101513', 'abnormal basal body', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(463183, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0141772', 'abnormal water homeostasis', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(463184, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0103083', 'abnormal dorsal lymph space morphology', 0.45161290322580644, 5.64885357140806, 1.5972148137558264, 'HP:0002715', 'Abnormality of the immune system'),
(463185, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0101366', 'abnormal morula cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(463186, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0100274', 'abnormal sensory system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(463187, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0115758', 'abnormally decreased mobility of melanoblast', 0.4444444444444444, 2.13901709234296, 0.9750252628847818, 'UPHENO:0075696', 'abnormal anatomical entity'),
(463188, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0100545', 'abnormal male organism', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463189, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0107276', 'abnormal dorsal region', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463190, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0100239', 'abnormal acellular anatomical structure', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463191, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0100956', 'abnormal centrosome', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(463192, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0107272', 'abnormal axial region', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463193, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0100070', 'abnormal anatomical system', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463194, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0101448', 'abnormal myelin accumulating cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(463195, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0101569', 'abnormal activin-induced ectoderm', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463196, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0101241', 'abnormal nucleate erythrocyte', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(463197, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0100377', 'abnormal connective tissue', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(463198, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0101467', 'abnormal alkali secreting cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(463199, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0126729', 'abnormally localised larval immune system', 0.42424242424242425, 5.64885357140806, 1.548057923116778, 'HP:0002715', 'Abnormality of the immune system'),
(463200, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0101200', 'abnormal joint region', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463201, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0141771', 'abnormal urea homeostasis', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(463202, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0100665', 'abnormal egg jelly', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463203, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0100429', 'abnormal spermatid', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(463204, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0101484', 'abnormal bone marrow', 0.41935483870967744, 5.64885357140806, 1.5391147060347428, 'HP:0002715', 'Abnormality of the immune system'),
(463205, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0100003', 'abnormal organism subdivision', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463206, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0100104', 'abnormal embryonic structure', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463207, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0126318', 'abnormally localised cell', 0.41379310344827586, 2.13901709234296, 0.9408031255100615, 'UPHENO:0075696', 'abnormal anatomical entity'),
(463208, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0100626', 'abnormal primordial germ cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(463209, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0100653', 'abnormal myoblast', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(463210, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0101570', 'abnormal forelimb region', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463211, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0101405', 'abnormal ring structure', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(463212, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0100062', 'abnormal anatomical space', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463213, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0100289', 'abnormal chondroblast', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(463214, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0100922', 'abnormal lymph vessel', 0.4117647058823529, 5.64885357140806, 1.525122463739656, 'HP:0002715', 'Abnormality of the immune system'),
(463215, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0100899', 'abnormal secondary spermatogonium', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(463216, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0126730', 'abnormally localised immune system', 0.45161290322580644, 5.64885357140806, 1.5972148137558264, 'HP:0002715', 'Abnormality of the immune system'),
(463217, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0125057', 'absent dorsal lymph space', 0.42424242424242425, 5.64885357140806, 1.548057923116778, 'HP:0002715', 'Abnormality of the immune system'),
(463218, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0101132', 'abnormal apoptotic cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(463219, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0115505', 'dead whole organism', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463220, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0101264', 'abnormal mitotic spindle', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(463221, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0101713', 'abnormal anatomical entity in vitro morphology', 0.43478260869565216, 2.13901709234296, 0.9643689291207286, 'UPHENO:0075696', 'abnormal anatomical entity'),
(463222, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0141745', 'abnormal creatinine homeostasis', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(463223, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0100745', 'abnormal anterior lymph sac', 0.5, 5.64885357140806, 1.6806031017774632, 'HP:0002715', 'Abnormality of the immune system'),
(463224, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0100258', 'abnormal organ part', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463225, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0100902', 'abnormal spermatocyte', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(463226, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0100573', 'abnormal extraembryonic structure', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463227, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0141266', 'abnormal surface breathing', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(463228, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0100728', 'abnormal cell condensation', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463229, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0131667', 'abnormal actin cytoskeleton', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(463230, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0101468', 'abnormal stage I oocyte', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(463231, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0100232', 'abnormal lymphatic system', 0.5652173913043478, 5.64885357140806, 1.786849260427838, 'HP:0002715', 'Abnormality of the immune system'),
(463232, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0101202', 'abnormal thymus', 0.40625, 5.64885357140806, 1.5148751642906173, 'HP:0002715', 'Abnormality of the immune system'),
(463233, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0100976', 'abnormal multiciliated cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(463234, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0100427', 'abnormal olfactory system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(463235, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0100014', 'abnormal tissue', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463236, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0100025', 'abnormal oocyte', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(463237, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0131677', 'abnormal actin filament', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(463238, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0141616', 'metaplastic left lymph heart', 0.45161290322580644, 5.64885357140806, 1.5972148137558264, 'HP:0002715', 'Abnormality of the immune system'),
(463239, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0100242', 'abnormal right lymph heart', 0.4642857142857143, 5.64885357140806, 1.6194696710023933, 'HP:0002715', 'Abnormality of the immune system'),
(463240, 'HP:0010978', 'Abnormality of immune system physiology', 'XPO:0100422', 'abnormal notochord', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(463241, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0100009', 'abnormal multi-tissue structure', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463242, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0101547', 'abnormal lampbrush chromosome', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(463243, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0101220', 'abnormal centriole', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(463244, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0100917', 'abnormal stage III oocyte', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(463245, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0131685', 'abnormal cortical actin cytoskeleton', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(463246, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0100337', 'abnormal zygote', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(463247, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0100225', 'abnormal endocrine system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(463248, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0107284', 'abnormal migrating myoblast', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(463249, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0100392', 'abnormal cilium', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(463250, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0100545', 'abnormal male organism', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463251, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0101373', 'abnormal oxygen accumulating cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(463252, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0100784', 'abnormal left blastomere', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(463253, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0101302', 'abnormal subcortical cytoplasm', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(463254, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0101535', 'abnormal absorptive cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(463255, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0100152', 'abnormal alimentary system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(463256, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0100026', 'abnormal germ cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(463257, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0107263', 'abnormal anatomical side', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463258, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0101132', 'abnormal apoptotic cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(463259, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0101569', 'abnormal activin-induced ectoderm', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463260, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0100172', 'abnormal stem cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(463261, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0101497', 'abnormal ciliary axoneme', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(463262, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0115509', 'abnormally semi-viable whole organism', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463263, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0101409', 'abnormal perivitelline space', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(463264, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0100989', 'abnormal right blastomere', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(463265, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0101513', 'abnormal basal body', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(463266, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0101326', 'abnormal cementoblast', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(463267, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0100551', 'abnormal oocyte cortex', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(463268, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0101240', 'abnormal ciliated non-epidermal cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(463269, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0100715', 'abnormal ciliated cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(463270, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0107272', 'abnormal axial region', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463271, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0141263', 'abnormal visually guided collision avoidance behavior', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(463272, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0100295', 'abnormal extracellular matrix', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463273, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0100014', 'abnormal tissue', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463274, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0100503', 'abnormal blastomere D2', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(463275, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0100581', 'abnormal immune system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(463276, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0107278', 'abnormal medial region', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463277, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0100003', 'abnormal organism subdivision', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463278, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0101389', 'abnormal wedge region', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(463279, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0101451', 'abnormal dorsal lymph space', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(463280, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0141499', 'abnormal tadpole', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463281, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0101136', 'abnormal ooplasm', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(463282, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0101333', 'abnormal barrier epithelial cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(463283, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0101109', 'abnormal egg cell-free extract', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463284, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0100515', 'abnormal somatic stem cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(463285, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0100721', 'abnormal centromere', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(463286, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0100688', 'abnormal adipose tissue', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(463287, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0107262', 'abnormal left-right axis', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463288, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0100728', 'abnormal cell condensation', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463289, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0107276', 'abnormal dorsal region', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463290, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0100574', 'abnormal gastrula cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(463291, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0100907', 'abnormal cytoplasm', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(463292, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0100108', 'abnormal cell part', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(463293, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0100427', 'abnormal olfactory system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(463294, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0100547', 'abnormal blastomere V2', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(463295, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0100501', 'abnormal urogenital system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(463296, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0100273', 'abnormal visual system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(463297, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0141745', 'abnormal creatinine homeostasis', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(463298, 'HP:0025674', 'Meconium pseudocyst', 'XPO:00000000', 'Xenopus phenotype', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(463299, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0107273', 'abnormal basal region', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463300, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0101071', 'abnormal endoplasmic reticulum', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(463301, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0107271', 'abnormal apical region', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463302, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0101311', 'abnormal bottle cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(463303, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0100006', 'abnormal anatomical structure', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463304, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0141272', 'absent surface breathing', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(463305, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0142057', 'abnormal desmosome', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(463306, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0100862', 'abnormal blastomere V1', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(463307, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0100477', 'abnormal pericyte', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(463308, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0131666', 'abnormal adherens junction', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(463309, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0100386', 'abnormal limb', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(463310, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0101061', 'abnormal plasma membrane', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(463311, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0100422', 'abnormal notochord', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(463312, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0141776', 'abnormal metabolic process', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(463313, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0131677', 'abnormal actin filament', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(463314, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0107312', 'abnormal filopodium', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(463315, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0100232', 'abnormal lymphatic system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(463316, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0101347', 'abnormal hindlimb region', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463317, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0100842', 'abnormal left-dorsal blastomere', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(463318, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0100372', 'abnormal hematological system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(463319, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0100533', 'abnormal melanoblast', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(463320, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0101498', 'abnormal stage II oocyte', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(463321, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0101435', 'abnormal paracrine cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(463322, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0100902', 'abnormal spermatocyte', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(463323, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0100317', 'abnormal respiratory system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(463324, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0141772', 'abnormal water homeostasis', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(463325, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0101072', 'abnormal mitochondrial cloud', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(463326, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0101405', 'abnormal ring structure', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(463327, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0107339', 'abnormal yolk platelet', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(463328, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0100642', 'abnormal gustatory system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(463329, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0100289', 'abnormal chondroblast', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(463330, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0100104', 'abnormal embryonic structure', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463331, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0100176', 'abnormal stage VI oocyte', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(463332, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0100025', 'abnormal oocyte', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(463333, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0100437', 'abnormal proepicardium', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(463334, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0100258', 'abnormal organ part', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463335, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0141771', 'abnormal urea homeostasis', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(463336, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0131725', 'abnormal phosphorylation of RNA polymerase II C-terminal domain', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(463337, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0141315', 'abnormal anatomical region', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463338, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0101472', 'abnormal zygote cortex', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(463339, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0101448', 'abnormal myelin accumulating cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(463340, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0100010', 'abnormal multicellular anatomical structure', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463341, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0100665', 'abnormal egg jelly', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463342, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0141267', 'abnormal resting posture', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(463343, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0100377', 'abnormal connective tissue', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(463344, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0100791', 'abnormal multiciliated cell precursor', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(463345, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0100084', 'abnormal anatomical group', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463346, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0100638', 'abnormal polar body', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(463347, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0100218', 'abnormal epithelial cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(463348, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0101237', 'abnormal mucus secreting cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(463349, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0131723', 'abnormal pathway-restricted SMAD protein phosphorylation', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(463350, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0100429', 'abnormal spermatid', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(463351, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0131669', 'abnormal Roux spot', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(463352, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0141266', 'abnormal surface breathing', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(463353, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0101297', 'abnormal barrier cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(463354, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0100549', 'abnormal mitotic cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(463355, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0100308', 'abnormal early embryonic cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(463356, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0101461', 'abnormal sperm entry point', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(463357, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0100653', 'abnormal myoblast', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(463358, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0100823', 'abnormal blood', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(463359, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0100546', 'abnormal whole organism', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463360, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0115505', 'dead whole organism', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463361, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0100899', 'abnormal secondary spermatogonium', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(463362, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0100274', 'abnormal sensory system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(463363, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0100417', 'abnormal dense regular connective tissue', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(463364, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0100081', 'abnormal anatomical entity in vitro', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463365, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0107270', 'abnormal proximal-distal axis', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463366, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0141784', 'abnormal cellular hormone metabolic process', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(463367, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0141265', 'abnormal escape behavior', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(463368, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0101113', 'abnormal stage IV oocyte', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(463369, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0141264', 'abnormal schooling behavior', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(463370, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0101141', 'abnormal Keller explant', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463371, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0101575', 'abnormal vitelline membrane', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(463372, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0101570', 'abnormal forelimb region', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463373, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0101411', 'abnormal marginal zone (sensu neural)', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463374, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0100028', 'abnormal anatomical cluster', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463375, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0100202', 'abnormal embryo', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463376, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0100887', 'abnormal right-dorsal blastomere', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(463377, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0101110', 'abnormal cell-free extract', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463378, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0101264', 'abnormal mitotic spindle', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(463379, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0100888', 'abnormal microtubule', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(463380, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0101228', 'abnormal mesenchymal stem cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(463381, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0100573', 'abnormal extraembryonic structure', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463382, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0100285', 'abnormal progenitor cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(463383, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0100004', 'abnormal cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(463384, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0100754', 'abnormal electrically active cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(463385, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0115508', 'abnormally peramorphic growth of whole organism', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463386, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0100704', 'abnormal Merkel cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(463387, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0141738', 'abnormal carbon dioxide homeostasis', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(463388, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0100070', 'abnormal anatomical system', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463389, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0100956', 'abnormal centrosome', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(463390, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0100724', 'abnormal kinetochore', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(463391, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0100307', 'abnormal blastomere', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(463392, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0100599', 'abnormal adult immune system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(463393, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0100643', 'abnormal thoracic region', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463394, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0107259', 'abnormal animal-vegetal axis', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463395, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0107253', 'abnormal enteric nervous system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(463396, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0100062', 'abnormal anatomical space', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463397, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0101283', 'abnormal left-ventral blastomere', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(463398, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0100626', 'abnormal primordial germ cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(463399, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0100032', 'abnormal nervous system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(463400, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0100481', 'abnormal anatomical line', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463401, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0100423', 'abnormal process', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463402, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0101221', 'abnormal larval immune system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(463403, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0100691', 'abnormal keratin accumulating cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(463404, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0107260', 'abnormal anterior-posterior axis', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463405, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0131675', 'abnormal spindle microtubule', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(463406, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0100762', 'abnormal intersomitic region', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463407, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0101241', 'abnormal nucleate erythrocyte', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(463408, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0107261', 'abnormal dorsal-ventral axis', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463409, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0107258', 'abnormal anatomical axis', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463410, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0100894', 'abnormal nucleus', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(463411, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0100585', 'abnormal elastica externa', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(463412, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0141743', 'abnormal chemical homeostasis within a tissue', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(463413, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0100239', 'abnormal acellular anatomical structure', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463414, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0100674', 'abnormal secondary oogonium', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(463415, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0100969', 'abnormal disaggregated/reaggregated ectoderm treated with activin', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463416, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0101157', 'abnormal female organism', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463417, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0101004', 'abnormal acid secreting cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(463418, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0100344', 'abnormal portion of organism substance', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463419, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0100277', 'abnormal blastocoel', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463420, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0101467', 'abnormal alkali secreting cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(463421, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0131667', 'abnormal actin cytoskeleton', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(463422, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0101468', 'abnormal stage I oocyte', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(463423, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0101480', 'abnormal stage V oocyte', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(463424, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0115512', 'abnormally semi-erect whole organism', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463425, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0141748', 'abnormal gas homeostasis', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(463426, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0100976', 'abnormal multiciliated cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(463427, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0100465', 'abnormal skeletal system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(463428, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0101463', 'abnormal right-ventral blastomere', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(463429, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0100852', 'abnormal interdigital region', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(463430, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0131687', 'abnormal astral microtubule', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(463431, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0100205', 'abnormal limb segment', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(463432, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0141770', 'abnormal urate homeostasis', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(463433, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0101200', 'abnormal joint region', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463434, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0100802', 'abnormal exocrine cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(463435, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0100587', 'abnormal vestibuloauditory system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(463436, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0101378', 'abnormal blastomere D1', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(463437, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0101366', 'abnormal morula cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(463438, 'HP:0025674', 'Meconium pseudocyst', 'XPO:0100031', 'abnormal central nervous system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(463439, 'HP:0000584', 'Punctate corneal epithelial erosions', 'XPO:0115423', 'abnormally incomplete structure of eye', 0.4246575342465753, 6.887869297006056, 1.7102589253909142, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(463440, 'HP:0000584', 'Punctate corneal epithelial erosions', 'XPO:0127907', 'abnormally localised optic choroid vascular plexus', 0.40789473684210525, 6.887869297006056, 1.6761639640277146, 'HP:0012372', 'Abnormal eye morphology'),
(463441, 'HP:0000584', 'Punctate corneal epithelial erosions', 'XPO:0102476', 'abnormal lens transitional zone morphology', 0.4533333333333333, 9.014833150514745, 2.021564829919309, 'UPHENO:0021038', 'abnormal anterior segment of eyeball morphology'),
(463442, 'HP:0000584', 'Punctate corneal epithelial erosions', 'XPO:0140375', 'abnormally necrotic lens', 0.4358974358974359, 9.014833150514745, 1.982307406875276, 'UPHENO:0021038', 'abnormal anterior segment of eyeball morphology'),
(463443, 'HP:0000584', 'Punctate corneal epithelial erosions', 'XPO:0101823', 'abnormal lens epithelium morphology', 0.4146341463414634, 9.014833150514745, 1.9333539892565992, 'UPHENO:0021038', 'abnormal anterior segment of eyeball morphology'),
(463444, 'HP:0000584', 'Punctate corneal epithelial erosions', 'XPO:0141141', 'abnormally necrotic cornea', 0.4810126582278481, 10.582693223545188, 2.256193564095799, 'UPHENO:0020998', 'abnormal cornea morphology'),
(463445, 'HP:0000584', 'Punctate corneal epithelial erosions', 'XPO:0133354', 'fused eyes', 0.41333333333333333, 6.887869297006056, 1.6873013886368484, 'HP:0012372', 'Abnormal eye morphology'),
(463446, 'HP:0000584', 'Punctate corneal epithelial erosions', 'XPO:0140250', 'abnormally necrotic iris', 0.40476190476190477, 9.014833150514745, 1.910199213986099, 'UPHENO:0021038', 'abnormal anterior segment of eyeball morphology'),
(463447, 'HP:0000584', 'Punctate corneal epithelial erosions', 'XPO:0133371', 'eye fused with olfactory pit', 0.41333333333333333, 6.887869297006056, 1.6873013886368484, 'HP:0012372', 'Abnormal eye morphology'),
(463448, 'HP:0000584', 'Punctate corneal epithelial erosions', 'XPO:0130893', 'increased size of the pupil', 0.40476190476190477, 9.014833150514745, 1.910199213986099, 'UPHENO:0021038', 'abnormal anterior segment of eyeball morphology'),
(463449, 'HP:0000584', 'Punctate corneal epithelial erosions', 'XPO:0141343', 'decreased pigmentation in the eye', 0.41333333333333333, 6.887869297006056, 1.6873013886368484, 'HP:0012372', 'Abnormal eye morphology'),
(463450, 'HP:0000584', 'Punctate corneal epithelial erosions', 'XPO:0102805', 'abnormal retinal layer morphology', 0.4025974025974026, 6.887869297006056, 1.6652442128423794, 'HP:0012372', 'Abnormal eye morphology'),
(463451, 'HP:0000584', 'Punctate corneal epithelial erosions', 'XPO:0133372', 'eye fused with olfactory epithelium', 0.41333333333333333, 6.887869297006056, 1.6873013886368484, 'HP:0012372', 'Abnormal eye morphology'),
(463452, 'HP:0000584', 'Punctate corneal epithelial erosions', 'XPO:0130736', 'increased size of the cornea', 0.4470588235294118, 10.582693223545188, 2.1751060623084086, 'UPHENO:0020998', 'abnormal cornea morphology'),
(463453, 'HP:0000584', 'Punctate corneal epithelial erosions', 'XPO:0103048', 'abnormal cornea morphology', 0.5205479452054794, 10.582693223545188, 2.347083128535587, 'UPHENO:0020998', 'abnormal cornea morphology'),
(463454, 'HP:0000584', 'Punctate corneal epithelial erosions', 'XPO:0103022', 'abnormal ciliary body morphology', 0.4050632911392405, 8.412768222102876, 1.8459966369515974, 'UPHENO:0087597', 'abnormal anterior segment of eyeball morphology'),
(463455, 'HP:0000584', 'Punctate corneal epithelial erosions', 'XPO:0133369', 'eye fused with brain', 0.41333333333333333, 6.887869297006056, 1.6873013886368484, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(463456, 'HP:0000584', 'Punctate corneal epithelial erosions', 'XPO:0102550', 'abnormal lens morphology', 0.4657534246575342, 9.014833150514745, 2.0490703776514145, 'UPHENO:0021038', 'abnormal anterior segment of eyeball morphology'),
(463457, 'HP:0000584', 'Punctate corneal epithelial erosions', 'XPO:0100371', 'abnormal hyaloid blood vessel', 0.484375, 6.887869297006056, 1.8265573330003382, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(463458, 'HP:0000584', 'Punctate corneal epithelial erosions', 'XPO:0141323', 'edematous eye', 0.4189189189189189, 6.887869297006056, 1.6986638159319787, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(463459, 'HP:0000584', 'Punctate corneal epithelial erosions', 'XPO:0100710', 'abnormal hyaloid vein', 0.4696969696969697, 6.887869297006056, 1.7986693238259617, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(463460, 'HP:0000584', 'Punctate corneal epithelial erosions', 'XPO:0141638', 'neoplastic eye', 0.41333333333333333, 6.887869297006056, 1.6873013886368484, 'HP:0012372', 'Abnormal eye morphology'),
(463461, 'HP:0000584', 'Punctate corneal epithelial erosions', 'XPO:0128467', 'decreased size of the lens', 0.41975308641975306, 9.014833150514745, 1.9452516645636548, 'UPHENO:0021038', 'abnormal anterior segment of eyeball morphology'),
(463462, 'HP:0000584', 'Punctate corneal epithelial erosions', 'XPO:0130285', 'increased size of the lens transitional zone', 0.4146341463414634, 9.014833150514745, 1.9333539892565992, 'UPHENO:0021038', 'abnormal anterior segment of eyeball morphology'),
(463463, 'HP:0000584', 'Punctate corneal epithelial erosions', 'XPO:0101315', 'abnormal hyaloid vascular plexus', 0.4696969696969697, 6.887869297006056, 1.7986693238259617, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(463464, 'HP:0000584', 'Punctate corneal epithelial erosions', 'XPO:0129260', 'decreased size of the cornea', 0.4470588235294118, 10.582693223545188, 2.1751060623084086, 'UPHENO:0020998', 'abnormal cornea morphology'),
(463465, 'HP:0000584', 'Punctate corneal epithelial erosions', 'XPO:0102003', 'abnormal hyaloid blood vessel morphology', 0.4025974025974026, 6.887869297006056, 1.6652442128423794, 'HP:0012372', 'Abnormal eye morphology'),
(463466, 'HP:0000584', 'Punctate corneal epithelial erosions', 'XPO:0102513', 'abnormal sclera morphology', 0.4246575342465753, 6.887869297006056, 1.7102589253909142, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(463467, 'HP:0000584', 'Punctate corneal epithelial erosions', 'XPO:0127645', 'abnormally localised hyaloid vein', 0.4025974025974026, 6.887869297006056, 1.6652442128423794, 'HP:0012372', 'Abnormal eye morphology'),
(463468, 'HP:0000584', 'Punctate corneal epithelial erosions', 'XPO:0127230', 'abnormally localised hyaloid blood vessel', 0.4246575342465753, 6.887869297006056, 1.7102589253909142, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(463469, 'HP:0000584', 'Punctate corneal epithelial erosions', 'XPO:0101817', 'abnormal eye morphology', 0.4305555555555556, 6.887869297006056, 1.7220947685207388, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(463470, 'HP:0000584', 'Punctate corneal epithelial erosions', 'XPO:0128807', 'decreased size of the lens transitional zone', 0.4146341463414634, 9.014833150514745, 1.9333539892565992, 'UPHENO:0021038', 'abnormal anterior segment of eyeball morphology'),
(463471, 'HP:0000584', 'Punctate corneal epithelial erosions', 'XPO:0100779', 'abnormal optic choroid vascular plexus', 0.47692307692307695, 6.887869297006056, 1.8124524320853552, 'HP:0012372', 'Abnormal eye morphology'),
(463472, 'HP:0000584', 'Punctate corneal epithelial erosions', 'XPO:0140473', 'abnormally necrotic lens transitional zone', 0.425, 9.014833150514745, 1.957371729889028, 'UPHENO:0021038', 'abnormal anterior segment of eyeball morphology'),
(463473, 'HP:0000584', 'Punctate corneal epithelial erosions', 'XPO:0141337', 'increased pigmentation in the eye', 0.41333333333333333, 6.887869297006056, 1.6873013886368484, 'HP:0012372', 'Abnormal eye morphology'),
(463474, 'HP:0000584', 'Punctate corneal epithelial erosions', 'XPO:0103210', 'abnormal pupil morphology', 0.43037974683544306, 9.014833150514745, 1.969721200851099, 'UPHENO:0021038', 'abnormal anterior segment of eyeball morphology'),
(463475, 'HP:0000584', 'Punctate corneal epithelial erosions', 'XPO:0102862', 'abnormal iris morphology', 0.43037974683544306, 9.014833150514745, 1.969721200851099, 'UPHENO:0021038', 'abnormal anterior segment of eyeball morphology'),
(463476, 'HP:0000584', 'Punctate corneal epithelial erosions', 'XPO:0125589', 'absent hyaloid blood vessel', 0.40789473684210525, 6.887869297006056, 1.6761639640277146, 'HP:0012372', 'Abnormal eye morphology'),
(463477, 'HP:0000584', 'Punctate corneal epithelial erosions', 'XPO:0129947', 'increased size of the lens', 0.41975308641975306, 9.014833150514745, 1.9452516645636548, 'UPHENO:0021038', 'abnormal anterior segment of eyeball morphology'),
(463478, 'HP:0033320', 'Mesangial cell loss', 'XPO:0103061', 'abnormal glomerular mesangial cell morphology', 0.47368421052631576, 9.777421615988073, 2.152071151043163, 'HP:0000095', 'Abnormal renal glomerulus morphology'),
(463479, 'HP:0033320', 'Mesangial cell loss', 'XPO:0101779', 'abnormal mesonephric mesenchyme morphology', 0.43333333333333335, 7.603795021646889, 1.8152073828391213, 'HP:0012210', 'Abnormal renal morphology'),
(463480, 'HP:0033320', 'Mesangial cell loss', 'XPO:0129137', 'decreased size of the glomeral nexus', 0.45569620253164556, 9.777421615988073, 2.110813563760805, 'HP:0000095', 'Abnormal renal glomerulus morphology'),
(463481, 'HP:0033320', 'Mesangial cell loss', 'XPO:0107388', 'abnormal adult kidney morphology', 0.4262295081967213, 7.603795021646889, 1.800267150315539, 'HP:0012210', 'Abnormal renal morphology'),
(463482, 'HP:0033320', 'Mesangial cell loss', 'XPO:0128301', 'decreased size of the glomus', 0.47368421052631576, 9.777421615988073, 2.152071151043163, 'HP:0000095', 'Abnormal renal glomerulus morphology'),
(463483, 'HP:0033320', 'Mesangial cell loss', 'XPO:0130613', 'increased size of the glomeral nexus', 0.45569620253164556, 9.777421615988073, 2.110813563760805, 'HP:0000095', 'Abnormal renal glomerulus morphology'),
(463484, 'HP:0033320', 'Mesangial cell loss', 'XPO:0141643', 'neoplastic kidney', 0.41935483870967744, 7.603795021646889, 1.7856898484575028, 'HP:0012210', 'Abnormal renal morphology'),
(463485, 'HP:0033320', 'Mesangial cell loss', 'XPO:0141107', 'abnormally necrotic glomerular epithelial cell', 0.43373493975903615, 9.777421615988073, 2.0593225525908476, 'HP:0000095', 'Abnormal renal glomerulus morphology'),
(463486, 'HP:0033320', 'Mesangial cell loss', 'XPO:0129279', 'decreased size of the glomerulus', 0.4931506849315068, 9.777421615988073, 2.195846571777873, 'HP:0000095', 'Abnormal renal glomerulus morphology'),
(463487, 'HP:0033320', 'Mesangial cell loss', 'XPO:0128487', 'decreased size of the podocyte', 0.4186046511627907, 9.777421615988073, 2.0230853083427345, 'HP:0000095', 'Abnormal renal glomerulus morphology'),
(463488, 'HP:0033320', 'Mesangial cell loss', 'XPO:0129202', 'decreased size of the mesonephric sinus', 0.45614035087719296, 7.603795021646889, 1.8623634793380868, 'HP:0012210', 'Abnormal renal morphology'),
(463489, 'HP:0033320', 'Mesangial cell loss', 'XPO:0129639', 'increased size of the mesonephric nephron', 0.4027777777777778, 8.69044940390107, 1.8709141879823046, 'UPHENO:0076756', 'abnormal nephron morphology'),
(463490, 'HP:0033320', 'Mesangial cell loss', 'XPO:0102837', 'abnormal glomerular epithelial cell morphology', 0.46153846153846156, 9.777421615988073, 2.124301327603039, 'HP:0000095', 'Abnormal renal glomerulus morphology'),
(463491, 'HP:0033320', 'Mesangial cell loss', 'XPO:0140478', 'abnormally necrotic glomerulus', 0.5070422535211268, 9.777421615988073, 2.226559204197537, 'HP:0000095', 'Abnormal renal glomerulus morphology'),
(463492, 'HP:0033320', 'Mesangial cell loss', 'XPO:0128865', 'decreased size of the glomerular mesangial cell', 0.4044943820224719, 9.777421615988073, 1.9886960839535672, 'HP:0000095', 'Abnormal renal glomerulus morphology'),
(463493, 'HP:0033320', 'Mesangial cell loss', 'XPO:0102909', 'abnormal glomerulus morphology', 0.5454545454545454, 9.777421615988073, 2.3093590156721455, 'HP:0000095', 'Abnormal renal glomerulus morphology'),
(463494, 'HP:0033320', 'Mesangial cell loss', 'XPO:0107387', 'abnormal embryonic kidney morphology', 0.4262295081967213, 7.603795021646889, 1.800267150315539, 'HP:0012210', 'Abnormal renal morphology'),
(463495, 'HP:0033320', 'Mesangial cell loss', 'XPO:0101903', 'abnormal mesonephric nephron morphology', 0.4461538461538462, 8.69044940390107, 1.9690803504062149, 'UPHENO:0076756', 'abnormal nephron morphology'),
(463496, 'HP:0033320', 'Mesangial cell loss', 'XPO:0101902', 'abnormal mesonephric tubule morphology', 0.4084507042253521, 8.69044940390107, 1.8840435714330452, 'UPHENO:0076756', 'abnormal nephron morphology'),
(463497, 'HP:0033320', 'Mesangial cell loss', 'XPO:0139856', 'abnormally necrotic glomeral nexus', 0.46153846153846156, 9.777421615988073, 2.124301327603039, 'HP:0000095', 'Abnormal renal glomerulus morphology'),
(463498, 'HP:0033320', 'Mesangial cell loss', 'XPO:0130343', 'increased size of the glomerular mesangial cell', 0.4044943820224719, 9.777421615988073, 1.9886960839535672, 'HP:0000095', 'Abnormal renal glomerulus morphology'),
(463499, 'HP:0033320', 'Mesangial cell loss', 'XPO:0129781', 'increased size of the glomus', 0.46153846153846156, 9.777421615988073, 2.124301327603039, 'HP:0000095', 'Abnormal renal glomerulus morphology'),
(463500, 'HP:0033320', 'Mesangial cell loss', 'XPO:0128159', 'decreased size of the mesonephric nephron', 0.4027777777777778, 8.69044940390107, 1.8709141879823046, 'UPHENO:0076756', 'abnormal nephron morphology'),
(463501, 'HP:0033320', 'Mesangial cell loss', 'XPO:0102671', 'abnormal glomeral nexus morphology', 0.5, 9.777421615988073, 2.2110429231460063, 'HP:0000095', 'Abnormal renal glomerulus morphology'),
(463502, 'HP:0033320', 'Mesangial cell loss', 'XPO:0139909', 'abnormally necrotic mesonephric nephron', 0.4084507042253521, 8.69044940390107, 1.8840435714330452, 'UPHENO:0076756', 'abnormal nephron morphology'),
(463503, 'HP:0033320', 'Mesangial cell loss', 'XPO:0140005', 'abnormally necrotic glomus', 0.4864864864864865, 9.777421615988073, 2.1809593047232823, 'HP:0000095', 'Abnormal renal glomerulus morphology'),
(463504, 'HP:0033320', 'Mesangial cell loss', 'XPO:0140802', 'abnormally necrotic glomerular mesangial cell', 0.4444444444444444, 9.777421615988073, 2.08459125926809, 'HP:0000095', 'Abnormal renal glomerulus morphology'),
(463505, 'HP:0033320', 'Mesangial cell loss', 'XPO:0129967', 'increased size of the podocyte', 0.4186046511627907, 9.777421615988073, 2.0230853083427345, 'HP:0000095', 'Abnormal renal glomerulus morphology'),
(463506, 'HP:0033320', 'Mesangial cell loss', 'XPO:0102582', 'abnormal pronephric nephron morphology', 0.42028985507246375, 8.69044940390107, 1.9111535052109654, 'UPHENO:0076756', 'abnormal nephron morphology'),
(463507, 'HP:0033320', 'Mesangial cell loss', 'XPO:0101717', 'abnormal mesonephric sinus morphology', 0.5, 7.603795021646889, 1.9498455094759288, 'HP:0012210', 'Abnormal renal morphology'),
(463508, 'HP:0033320', 'Mesangial cell loss', 'XPO:0103049', 'abnormal podocyte morphology', 0.4864864864864865, 9.777421615988073, 2.1809593047232823, 'HP:0000095', 'Abnormal renal glomerulus morphology'),
(463509, 'HP:0033320', 'Mesangial cell loss', 'XPO:0130678', 'increased size of the mesonephric sinus', 0.45614035087719296, 7.603795021646889, 1.8623634793380868, 'HP:0012210', 'Abnormal renal morphology'),
(463510, 'HP:0033320', 'Mesangial cell loss', 'XPO:0102198', 'abnormal kidney morphology', 0.4406779661016949, 7.603795021646889, 1.8305258601815884, 'HP:0012210', 'Abnormal renal morphology'),
(463511, 'HP:0033320', 'Mesangial cell loss', 'XPO:0130755', 'increased size of the glomerulus', 0.48, 9.777421615988073, 2.166370784439791, 'HP:0000095', 'Abnormal renal glomerulus morphology'),
(463512, 'HP:0033320', 'Mesangial cell loss', 'XPO:0102040', 'abnormal glomus morphology', 0.5217391304347826, 9.777421615988073, 2.258597673739142, 'HP:0000095', 'Abnormal renal glomerulus morphology'),
(463513, 'HP:0033320', 'Mesangial cell loss', 'XPO:0140127', 'abnormally necrotic podocyte', 0.46153846153846156, 9.777421615988073, 2.124301327603039, 'HP:0000095', 'Abnormal renal glomerulus morphology'),
(463514, 'HP:0010674', 'Abnormal curvature of the vertebral column', 'XPO:0102272', 'abnormal notochordal sheath morphology', 0.5, 4.638757693672553, 1.5229507040072823, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(463515, 'HP:0010674', 'Abnormal curvature of the vertebral column', 'XPO:0103152', 'abnormal otic region morphology', 0.41818181818181815, 6.272837960958401, 1.6196255072310737, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(463516, 'HP:0010674', 'Abnormal curvature of the vertebral column', 'XPO:0102761', 'abnormal cartilaginous condensation morphology', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(463517, 'HP:0010674', 'Abnormal curvature of the vertebral column', 'XPO:0100422', 'abnormal notochord', 0.4117647058823529, 4.3395673355180735, 1.3367425584480601, 'UPHENO:0002964', 'abnormal skeletal system'),
(463518, 'HP:0010674', 'Abnormal curvature of the vertebral column', 'XPO:0102217', 'abnormal elastica externa morphology', 0.5263157894736842, 4.638757693672553, 1.5625144536043167, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(463519, 'HP:0010674', 'Abnormal curvature of the vertebral column', 'XPO:0140123', 'abnormally necrotic perichondrial cell', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(463520, 'HP:0010674', 'Abnormal curvature of the vertebral column', 'XPO:0128890', 'decreased size of the elastica externa', 0.4444444444444444, 4.638757693672553, 1.4358516936218344, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(463521, 'HP:0010674', 'Abnormal curvature of the vertebral column', 'XPO:0102401', 'abnormal neurocranium morphology', 0.41818181818181815, 6.272837960958401, 1.6196255072310737, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(463522, 'HP:0010674', 'Abnormal curvature of the vertebral column', 'XPO:0100927', 'abnormal sacral vertebra', 0.43103448275862066, 8.05344015541032, 1.863145300778979, 'UPHENO:0002813', 'abnormal vertebral column'),
(463523, 'HP:0010674', 'Abnormal curvature of the vertebral column', 'XPO:0130427', 'increased size of the vertebral centrum', 0.40625, 8.361863005979023, 1.843097079965941, 'UPHENO:0076695', 'abnormal vertebral column morphology'),
(463524, 'HP:0010674', 'Abnormal curvature of the vertebral column', 'XPO:0126886', 'abnormally localised vertebral column', 0.5102040816326531, 8.05344015541032, 2.0270416962841815, 'UPHENO:0002813', 'abnormal vertebral column'),
(463525, 'HP:0010674', 'Abnormal curvature of the vertebral column', 'XPO:0102567', 'abnormal skeleton morphology', 0.5, 4.638757693672553, 1.5229507040072823, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(463526, 'HP:0010674', 'Abnormal curvature of the vertebral column', 'XPO:0128132', 'decreased size of the perichondrium', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(463527, 'HP:0010674', 'Abnormal curvature of the vertebral column', 'XPO:0102054', 'abnormal notochord morphology', 0.5, 4.638757693672553, 1.5229507040072823, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(463528, 'HP:0010674', 'Abnormal curvature of the vertebral column', 'XPO:0140350', 'abnormally necrotic notochordal sheath', 0.4444444444444444, 4.638757693672553, 1.4358516936218344, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(463529, 'HP:0010674', 'Abnormal curvature of the vertebral column', 'XPO:0128246', 'decreased size of the axial skeleton', 0.4117647058823529, 6.211345574613551, 1.599253852164941, 'UPHENO:0087089', 'abnormal axial skeleton plus cranial skeleton morphology'),
(463530, 'HP:0010674', 'Abnormal curvature of the vertebral column', 'XPO:0102216', 'abnormal vertebral column morphology', 0.5777777777777777, 8.361863005979023, 2.1980215252987785, 'UPHENO:0076695', 'abnormal vertebral column morphology'),
(463531, 'HP:0010674', 'Abnormal curvature of the vertebral column', 'XPO:0139998', 'abnormally necrotic axial skeleton', 0.42857142857142855, 6.211345574613551, 1.6315652749010534, 'UPHENO:0087089', 'abnormal axial skeleton plus cranial skeleton morphology'),
(463532, 'HP:0010674', 'Abnormal curvature of the vertebral column', 'XPO:0140432', 'abnormally necrotic skeleton', 0.4444444444444444, 4.638757693672553, 1.4358516936218344, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(463533, 'HP:0010674', 'Abnormal curvature of the vertebral column', 'XPO:0127548', 'abnormally localised vertebral element', 0.43859649122807015, 8.05344015541032, 1.8794176210938882, 'UPHENO:0002813', 'abnormal vertebral column'),
(463534, 'HP:0010674', 'Abnormal curvature of the vertebral column', 'XPO:0129877', 'increased size of the cranial skeleton', 0.40384615384615385, 6.211345574613551, 1.5838017617482976, 'UPHENO:0087089', 'abnormal axial skeleton plus cranial skeleton morphology'),
(463535, 'HP:0010674', 'Abnormal curvature of the vertebral column', 'XPO:0140144', 'abnormally necrotic portion of organism substance', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(463536, 'HP:0010674', 'Abnormal curvature of the vertebral column', 'XPO:0100693', 'abnormal vertebral centrum', 0.5319148936170213, 8.05344015541032, 2.0697209385605895, 'UPHENO:0002813', 'abnormal vertebral column'),
(463537, 'HP:0010674', 'Abnormal curvature of the vertebral column', 'XPO:0102097', 'abnormal skeletal system morphology', 0.5263157894736842, 4.638757693672553, 1.5625144536043167, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(463538, 'HP:0010674', 'Abnormal curvature of the vertebral column', 'XPO:0130188', 'increased size of the flexural organ', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(463539, 'HP:0010674', 'Abnormal curvature of the vertebral column', 'XPO:0139795', 'abnormally necrotic vertebral element', 0.4262295081967213, 8.361863005979023, 1.8878751962581628, 'UPHENO:0076695', 'abnormal vertebral column morphology'),
(463540, 'HP:0010674', 'Abnormal curvature of the vertebral column', 'XPO:0100465', 'abnormal skeletal system', 0.4117647058823529, 4.3395673355180735, 1.3367425584480601, 'UPHENO:0002964', 'abnormal skeletal system'),
(463541, 'HP:0010674', 'Abnormal curvature of the vertebral column', 'XPO:0100253', 'abnormal vertebra', 0.43859649122807015, 8.05344015541032, 1.8794176210938882, 'UPHENO:0002813', 'abnormal vertebral column'),
(463542, 'HP:0010674', 'Abnormal curvature of the vertebral column', 'XPO:0128158', 'decreased size of the skeletal subdivision', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(463543, 'HP:0010674', 'Abnormal curvature of the vertebral column', 'XPO:0102164', 'abnormal mandibular mesenchyme morphology', 0.42857142857142855, 6.211345574613551, 1.6315652749010534, 'UPHENO:0087089', 'abnormal axial skeleton plus cranial skeleton morphology'),
(463544, 'HP:0010674', 'Abnormal curvature of the vertebral column', 'XPO:0140108', 'abnormally necrotic dermal skeleton', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(463545, 'HP:0010674', 'Abnormal curvature of the vertebral column', 'XPO:0128709', 'decreased size of the flexural organ', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(463546, 'HP:0010674', 'Abnormal curvature of the vertebral column', 'XPO:0101680', 'abnormal skeletal element morphology', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(463547, 'HP:0010674', 'Abnormal curvature of the vertebral column', 'XPO:0128949', 'decreased size of the vertebral centrum', 0.40625, 8.361863005979023, 1.843097079965941, 'UPHENO:0076695', 'abnormal vertebral column morphology'),
(463548, 'HP:0010674', 'Abnormal curvature of the vertebral column', 'XPO:0141703', 'abnormally necrotic posterior notochord', 0.4444444444444444, 4.638757693672553, 1.4358516936218344, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(463549, 'HP:0010674', 'Abnormal curvature of the vertebral column', 'XPO:0107345', 'abnormal anatomical axis morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(463550, 'HP:0010674', 'Abnormal curvature of the vertebral column', 'XPO:0141709', 'increased size of the anterior notochord', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(463551, 'HP:0010674', 'Abnormal curvature of the vertebral column', 'XPO:0100584', 'abnormal vertebral column', 0.625, 8.05344015541032, 2.2435240353362498, 'UPHENO:0002813', 'abnormal vertebral column'),
(463552, 'HP:0010674', 'Abnormal curvature of the vertebral column', 'XPO:0103116', 'abnormal bone marrow morphology', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(463553, 'HP:0010674', 'Abnormal curvature of the vertebral column', 'XPO:0129707', 'increased size of the vertebral column', 0.49056603773584906, 8.361863005979023, 2.025350834530429, 'UPHENO:0076695', 'abnormal vertebral column morphology'),
(463554, 'HP:0010674', 'Abnormal curvature of the vertebral column', 'XPO:0103355', 'decreased size of the notochord', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(463555, 'HP:0010674', 'Abnormal curvature of the vertebral column', 'XPO:0101226', 'abnormal postsacral vertebra', 0.43103448275862066, 8.05344015541032, 1.863145300778979, 'UPHENO:0002813', 'abnormal vertebral column'),
(463556, 'HP:0010674', 'Abnormal curvature of the vertebral column', 'XPO:0101070', 'abnormal rib', 0.423728813559322, 8.05344015541032, 1.8472884566637167, 'UPHENO:0002813', 'abnormal vertebral column'),
(463557, 'HP:0010674', 'Abnormal curvature of the vertebral column', 'XPO:0102009', 'abnormal connective tissue morphology', 0.41025641025641024, 3.9037819259951223, 1.2655242231512656, 'HP:0033127', 'Abnormality of the musculoskeletal system'),
(463558, 'HP:0010674', 'Abnormal curvature of the vertebral column', 'XPO:0129434', 'decreased size of the notochordal sheath', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(463559, 'HP:0010674', 'Abnormal curvature of the vertebral column', 'XPO:0128397', 'decreased size of the cranial skeleton', 0.40384615384615385, 6.211345574613551, 1.5838017617482976, 'UPHENO:0087089', 'abnormal axial skeleton plus cranial skeleton morphology'),
(463560, 'HP:0010674', 'Abnormal curvature of the vertebral column', 'XPO:0102806', 'abnormal articular system morphology', 0.5128205128205128, 4.638757693672553, 1.5423521320759594, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(463561, 'HP:0010674', 'Abnormal curvature of the vertebral column', 'XPO:0140683', 'abnormally necrotic flexural organ', 0.4444444444444444, 4.638757693672553, 1.4358516936218344, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(463562, 'HP:0010674', 'Abnormal curvature of the vertebral column', 'XPO:0102461', 'abnormal postcranial axial skeleton morphology', 0.5227272727272727, 6.272837960958401, 1.810796366130629, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(463563, 'HP:0010674', 'Abnormal curvature of the vertebral column', 'XPO:0125260', 'absent vertebral column', 0.4807692307692308, 8.05344015541032, 1.9677007466997247, 'UPHENO:0002813', 'abnormal vertebral column'),
(463564, 'HP:0010674', 'Abnormal curvature of the vertebral column', 'XPO:0130908', 'increased size of the notochordal sheath', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(463565, 'HP:0010674', 'Abnormal curvature of the vertebral column', 'XPO:0102773', 'abnormal Keller explant morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(463566, 'HP:0010674', 'Abnormal curvature of the vertebral column', 'XPO:0141723', 'abnormal posterior notochord morphology', 0.5, 4.638757693672553, 1.5229507040072823, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(463567, 'HP:0010674', 'Abnormal curvature of the vertebral column', 'XPO:0128727', 'decreased size of the vertebral element', 0.4126984126984127, 8.361863005979023, 1.8576672440911264, 'UPHENO:0076695', 'abnormal vertebral column morphology'),
(463568, 'HP:0010674', 'Abnormal curvature of the vertebral column', 'XPO:0130060', 'increased size of the postcranial axial skeleton', 0.4423076923076923, 6.272837960958401, 1.6656903922192745, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(463569, 'HP:0010674', 'Abnormal curvature of the vertebral column', 'XPO:0139718', 'abnormally necrotic anatomical structure', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(463570, 'HP:0010674', 'Abnormal curvature of the vertebral column', 'XPO:0139889', 'abnormally necrotic cranial skeleton', 0.42, 6.211345574613551, 1.61516721776344, 'UPHENO:0087089', 'abnormal axial skeleton plus cranial skeleton morphology'),
(463571, 'HP:0010674', 'Abnormal curvature of the vertebral column', 'XPO:0130368', 'increased size of the elastica externa', 0.4444444444444444, 4.638757693672553, 1.4358516936218344, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(463572, 'HP:0010674', 'Abnormal curvature of the vertebral column', 'XPO:0102178', 'abnormal whole organism morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(463573, 'HP:0010674', 'Abnormal curvature of the vertebral column', 'XPO:0102144', 'abnormal cranial skeleton morphology', 0.4772727272727273, 6.211345574613551, 1.7217740393063181, 'UPHENO:0087089', 'abnormal axial skeleton plus cranial skeleton morphology'),
(463574, 'HP:0010674', 'Abnormal curvature of the vertebral column', 'XPO:0102010', 'abnormal perichondrium morphology', 0.4878048780487805, 4.638757693672553, 1.5042634845863214, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(463575, 'HP:0010674', 'Abnormal curvature of the vertebral column', 'XPO:0107372', 'abnormal flexural organ morphology', 0.5, 4.638757693672553, 1.5229507040072823, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(463576, 'HP:0010674', 'Abnormal curvature of the vertebral column', 'XPO:0102542', 'abnormal vacuolated notochordal tissue morphology', 0.45454545454545453, 4.638757693672553, 1.452076521536181, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(463577, 'HP:0010674', 'Abnormal curvature of the vertebral column', 'XPO:0100252', 'abnormal caudal vertebra', 0.4166666666666667, 8.05344015541032, 1.8318297040812228, 'UPHENO:0002813', 'abnormal vertebral column'),
(463578, 'HP:0010674', 'Abnormal curvature of the vertebral column', 'XPO:0139771', 'abnormally necrotic skeletal subdivision', 0.43478260869565216, 4.638757693672553, 1.4201588541997616, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(463579, 'HP:0010674', 'Abnormal curvature of the vertebral column', 'XPO:0128306', 'decreased size of the articular system', 0.43478260869565216, 4.638757693672553, 1.4201588541997616, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(463580, 'HP:0010674', 'Abnormal curvature of the vertebral column', 'XPO:0140103', 'abnormally necrotic vertebral column', 0.5098039215686274, 8.361863005979023, 2.0646817072051897, 'UPHENO:0076695', 'abnormal vertebral column morphology'),
(463581, 'HP:0010674', 'Abnormal curvature of the vertebral column', 'XPO:0103218', 'abnormal joint morphology', 0.43478260869565216, 4.638757693672553, 1.4201588541997616, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(463582, 'HP:0010674', 'Abnormal curvature of the vertebral column', 'XPO:0102514', 'abnormal perichondrial cell morphology', 0.4444444444444444, 4.638757693672553, 1.4358516936218344, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(463583, 'HP:0010674', 'Abnormal curvature of the vertebral column', 'XPO:0103737', 'increased size of the notochord', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(463584, 'HP:0010674', 'Abnormal curvature of the vertebral column', 'XPO:0129664', 'increased size of the skeleton', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(463585, 'HP:0010674', 'Abnormal curvature of the vertebral column', 'XPO:0101890', 'abnormal organ part morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(463586, 'HP:0010674', 'Abnormal curvature of the vertebral column', 'XPO:0101860', 'abnormal skeletal subdivision morphology', 0.4878048780487805, 4.638757693672553, 1.5042634845863214, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(463587, 'HP:0010674', 'Abnormal curvature of the vertebral column', 'XPO:0102828', 'abnormal occipital region morphology', 0.42592592592592593, 6.272837960958401, 1.6345532468244968, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(463588, 'HP:0010674', 'Abnormal curvature of the vertebral column', 'XPO:0140019', 'abnormally necrotic skeletal system', 0.46511627906976744, 4.638757693672553, 1.4688640910537754, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(463589, 'HP:0010674', 'Abnormal curvature of the vertebral column', 'XPO:0128184', 'decreased size of the skeleton', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(463590, 'HP:0010674', 'Abnormal curvature of the vertebral column', 'XPO:0128580', 'decreased size of the postcranial axial skeleton', 0.4423076923076923, 6.272837960958401, 1.6656903922192745, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(463591, 'HP:0010674', 'Abnormal curvature of the vertebral column', 'XPO:0102605', 'abnormal dermal skeleton morphology', 0.46511627906976744, 4.638757693672553, 1.4688640910537754, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(463592, 'HP:0010674', 'Abnormal curvature of the vertebral column', 'XPO:0128227', 'decreased size of the vertebral column', 0.49056603773584906, 8.361863005979023, 2.025350834530429, 'UPHENO:0076695', 'abnormal vertebral column morphology'),
(463593, 'HP:0010674', 'Abnormal curvature of the vertebral column', 'XPO:0101694', 'abnormal anatomical space morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(463594, 'HP:0010674', 'Abnormal curvature of the vertebral column', 'XPO:0102113', 'abnormal anatomical line morphology', 0.43333333333333335, 2.786899518863159, 1.0989342374200721, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(463595, 'HP:0010674', 'Abnormal curvature of the vertebral column', 'XPO:0101981', 'abnormal ossicle morphology', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(463596, 'HP:0010674', 'Abnormal curvature of the vertebral column', 'XPO:0102130', 'abnormal endoskeleton morphology', 0.46511627906976744, 4.638757693672553, 1.4688640910537754, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(463597, 'HP:0010674', 'Abnormal curvature of the vertebral column', 'XPO:0140852', 'abnormally necrotic vertebral centrum', 0.41935483870967744, 8.361863005979023, 1.8725885058348382, 'UPHENO:0076695', 'abnormal vertebral column morphology'),
(463598, 'HP:0010674', 'Abnormal curvature of the vertebral column', 'XPO:0140812', 'abnormally necrotic endoskeleton', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(463599, 'HP:0010674', 'Abnormal curvature of the vertebral column', 'XPO:0129786', 'increased size of the articular system', 0.43478260869565216, 4.638757693672553, 1.4201588541997616, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(463600, 'HP:0010674', 'Abnormal curvature of the vertebral column', 'XPO:0139917', 'abnormally necrotic notochord', 0.43478260869565216, 4.638757693672553, 1.4201588541997616, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(463601, 'HP:0010674', 'Abnormal curvature of the vertebral column', 'XPO:0102601', 'abnormal disaggregated/reaggregated ectoderm treated with activin morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(463602, 'HP:0010674', 'Abnormal curvature of the vertebral column', 'XPO:0101957', 'abnormal axial skeleton morphology', 0.4883720930232558, 6.211345574613551, 1.7416796027871364, 'UPHENO:0087089', 'abnormal axial skeleton plus cranial skeleton morphology'),
(463603, 'HP:0010674', 'Abnormal curvature of the vertebral column', 'XPO:0102980', 'abnormal perichordal tissue morphology', 0.45454545454545453, 4.638757693672553, 1.452076521536181, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(463604, 'HP:0010674', 'Abnormal curvature of the vertebral column', 'XPO:0101755', 'abnormal pelvic girdle morphology', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(463605, 'HP:0010674', 'Abnormal curvature of the vertebral column', 'XPO:0125164', 'absent vertebral centrum', 0.4032258064516129, 8.05344015541032, 1.8020418700394085, 'UPHENO:0002813', 'abnormal vertebral column'),
(463606, 'HP:0010674', 'Abnormal curvature of the vertebral column', 'XPO:0128352', 'decreased size of the skeletal system', 0.4444444444444444, 4.638757693672553, 1.4358516936218344, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(463607, 'HP:0010674', 'Abnormal curvature of the vertebral column', 'XPO:0129612', 'increased size of the perichondrium', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(463608, 'HP:0010674', 'Abnormal curvature of the vertebral column', 'XPO:0126787', 'abnormally localised vertebral centrum', 0.43103448275862066, 8.05344015541032, 1.863145300778979, 'UPHENO:0002813', 'abnormal vertebral column'),
(463609, 'HP:0010674', 'Abnormal curvature of the vertebral column', 'XPO:0101740', 'abnormal cell part morphology', 0.4166666666666667, 2.786899518863159, 1.0775936770692605, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(463610, 'HP:0010674', 'Abnormal curvature of the vertebral column', 'XPO:0140559', 'abnormally necrotic articular system', 0.45454545454545453, 4.638757693672553, 1.452076521536181, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(463611, 'HP:0010674', 'Abnormal curvature of the vertebral column', 'XPO:0101982', 'abnormal appendicular skeleton morphology', 0.4444444444444444, 4.638757693672553, 1.4358516936218344, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(463612, 'HP:0010674', 'Abnormal curvature of the vertebral column', 'XPO:0139774', 'abnormally necrotic elastica externa', 0.46511627906976744, 4.638757693672553, 1.4688640910537754, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(463613, 'HP:0010674', 'Abnormal curvature of the vertebral column', 'XPO:0129726', 'increased size of the axial skeleton', 0.4117647058823529, 6.211345574613551, 1.599253852164941, 'UPHENO:0087089', 'abnormal axial skeleton plus cranial skeleton morphology'),
(463614, 'HP:0010674', 'Abnormal curvature of the vertebral column', 'XPO:0101446', 'abnormal transverse process', 0.423728813559322, 8.05344015541032, 1.8472884566637167, 'UPHENO:0002813', 'abnormal vertebral column'),
(463615, 'HP:0010674', 'Abnormal curvature of the vertebral column', 'XPO:0141713', 'increased size of the posterior notochord', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(463616, 'HP:0010674', 'Abnormal curvature of the vertebral column', 'XPO:0140043', 'abnormally necrotic perichondrium', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(463617, 'HP:0010674', 'Abnormal curvature of the vertebral column', 'XPO:0102093', 'abnormal craniofacial skeleton morphology', 0.45652173913043476, 6.211345574613551, 1.6839282300806968, 'UPHENO:0087089', 'abnormal axial skeleton plus cranial skeleton morphology'),
(463618, 'HP:0010674', 'Abnormal curvature of the vertebral column', 'XPO:0140510', 'abnormally necrotic postcranial axial skeleton', 0.46, 6.272837960958401, 1.69867756270602, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(463619, 'HP:0010674', 'Abnormal curvature of the vertebral column', 'XPO:0141699', 'abnormally necrotic anterior notochord', 0.4444444444444444, 4.638757693672553, 1.4358516936218344, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(463620, 'HP:0010674', 'Abnormal curvature of the vertebral column', 'XPO:0141708', 'decreased size of the posterior notochord', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(463621, 'HP:0010674', 'Abnormal curvature of the vertebral column', 'XPO:0101854', 'abnormal bone element morphology', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(463622, 'HP:0010674', 'Abnormal curvature of the vertebral column', 'XPO:0102564', 'abnormal olfactory region morphology', 0.41818181818181815, 6.272837960958401, 1.6196255072310737, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(463623, 'HP:0010674', 'Abnormal curvature of the vertebral column', 'XPO:0140269', 'abnormally necrotic anatomical line', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(463624, 'HP:0010674', 'Abnormal curvature of the vertebral column', 'XPO:0125894', 'absent vertebral element', 0.4098360655737705, 8.05344015541032, 1.816752660002781, 'UPHENO:0002813', 'abnormal vertebral column'),
(463625, 'HP:0010674', 'Abnormal curvature of the vertebral column', 'XPO:0103201', 'abnormal activin-induced ectoderm morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(463626, 'HP:0010674', 'Abnormal curvature of the vertebral column', 'XPO:0129832', 'increased size of the skeletal system', 0.4444444444444444, 4.638757693672553, 1.4358516936218344, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(463627, 'HP:0010674', 'Abnormal curvature of the vertebral column', 'XPO:0101858', 'abnormal vertebral element morphology', 0.49056603773584906, 8.361863005979023, 2.025350834530429, 'UPHENO:0076695', 'abnormal vertebral column morphology'),
(463628, 'HP:0010674', 'Abnormal curvature of the vertebral column', 'XPO:0102728', 'abnormal tendon morphology', 0.43478260869565216, 4.638757693672553, 1.4201588541997616, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(463629, 'HP:0010674', 'Abnormal curvature of the vertebral column', 'XPO:0102742', 'abnormal cell-free extract morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(463630, 'HP:0010674', 'Abnormal curvature of the vertebral column', 'XPO:0100226', 'abnormal vertebral element', 0.5434782608695652, 8.05344015541032, 2.0920969503537643, 'UPHENO:0002813', 'abnormal vertebral column'),
(463631, 'HP:0010674', 'Abnormal curvature of the vertebral column', 'XPO:0102351', 'abnormal sphenoid region morphology', 0.41818181818181815, 6.272837960958401, 1.6196255072310737, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(463632, 'HP:0010674', 'Abnormal curvature of the vertebral column', 'XPO:0141719', 'abnormal anterior notochord morphology', 0.5, 4.638757693672553, 1.5229507040072823, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(463633, 'HP:0010674', 'Abnormal curvature of the vertebral column', 'XPO:0100585', 'abnormal elastica externa', 0.42424242424242425, 4.3395673355180735, 1.3568450783281876, 'UPHENO:0002964', 'abnormal skeletal system'),
(463634, 'HP:0010674', 'Abnormal curvature of the vertebral column', 'XPO:0130205', 'increased size of the vertebral element', 0.4126984126984127, 8.361863005979023, 1.8576672440911264, 'UPHENO:0076695', 'abnormal vertebral column morphology'),
(463635, 'HP:0010674', 'Abnormal curvature of the vertebral column', 'XPO:0101636', 'abnormal cell morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(463636, 'HP:0010674', 'Abnormal curvature of the vertebral column', 'XPO:0101638', 'abnormal anatomical structure morphology', 0.43333333333333335, 2.786899518863159, 1.0989342374200721, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(463637, 'HP:0010674', 'Abnormal curvature of the vertebral column', 'XPO:0141704', 'decreased size of the anterior notochord', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(463638, 'HP:0010674', 'Abnormal curvature of the vertebral column', 'XPO:0101976', 'abnormal portion of organism substance morphology', 0.43333333333333335, 2.786899518863159, 1.0989342374200721, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(463639, 'HP:0010674', 'Abnormal curvature of the vertebral column', 'XPO:0102702', 'abnormal rib morphology', 0.40625, 8.361863005979023, 1.843097079965941, 'UPHENO:0076695', 'abnormal vertebral column morphology'),
(463640, 'HP:0010674', 'Abnormal curvature of the vertebral column', 'XPO:0100895', 'abnormal presacral vertebra', 0.43103448275862066, 8.05344015541032, 1.863145300778979, 'UPHENO:0002813', 'abnormal vertebral column'),
(463641, 'HP:0010674', 'Abnormal curvature of the vertebral column', 'XPO:0101713', 'abnormal anatomical entity in vitro morphology', 0.43333333333333335, 2.786899518863159, 1.0989342374200721, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(463642, 'HP:0010674', 'Abnormal curvature of the vertebral column', 'XPO:0129638', 'increased size of the skeletal subdivision', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(463643, 'HP:0010674', 'Abnormal curvature of the vertebral column', 'XPO:0141316', 'abnormal anatomical region morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(463644, 'HP:0010674', 'Abnormal curvature of the vertebral column', 'XPO:0102325', 'abnormal vertebral centrum morphology', 0.48148148148148145, 8.361863005979023, 2.006509952146755, 'UPHENO:0076695', 'abnormal vertebral column morphology'),
(463645, 'HP:0031185', 'Increased circulating NT-proBNP concentration', 'XPO:0141873', 'abnormal tricarboxylic acid metabolic process', 0.42592592592592593, 7.41682187759612, 1.7773622944247445, 'HP:0430071', 'Abnormal circulating organic compound concentration'),
(463646, 'HP:0007475', 'Congenital bullous ichthyosiform erythroderma', 'XPO:0130281', 'increased size of the dermis', 0.43636363636363634, 7.420886955069779, 1.7995013800377375, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(463647, 'HP:0007475', 'Congenital bullous ichthyosiform erythroderma', 'XPO:0102615', 'abnormal skin gland morphology', 0.42, 7.420886955069779, 1.7654383368244009, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(463648, 'HP:0007475', 'Congenital bullous ichthyosiform erythroderma', 'XPO:0129993', 'increased size of the Eberth-Kastschenko layer', 0.42105263157894735, 7.420886955069779, 1.7676492811307372, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(463649, 'HP:0007475', 'Congenital bullous ichthyosiform erythroderma', 'XPO:0129487', 'increased size of the anatomical structure', 0.42105263157894735, 5.972749669260594, 1.585825326448175, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(463650, 'HP:0007475', 'Congenital bullous ichthyosiform erythroderma', 'XPO:0130438', 'increased size of the granular gland', 0.41379310344827586, 7.420886955069779, 1.752344670285258, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(463651, 'HP:0007475', 'Congenital bullous ichthyosiform erythroderma', 'XPO:0128175', 'decreased size of the skin', 0.4107142857142857, 11.09310877090129, 2.1345018728479954, 'UPHENO:0081431', 'abnormal skin of body morphology in the independent continuant'),
(463652, 'HP:0007475', 'Congenital bullous ichthyosiform erythroderma', 'XPO:0129982', 'increased size of the anatomical line', 0.42105263157894735, 5.972749669260594, 1.585825326448175, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(463653, 'HP:0007475', 'Congenital bullous ichthyosiform erythroderma', 'XPO:0102139', 'abnormal skin morphology', 0.4489795918367347, 11.09310877090129, 2.2317211851303833, 'UPHENO:0081431', 'abnormal skin of body morphology in the independent continuant'),
(463654, 'HP:0007475', 'Congenital bullous ichthyosiform erythroderma', 'XPO:0130356', 'increased size of the skin gland', 0.43636363636363634, 7.420886955069779, 1.7995013800377375, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(463655, 'HP:0007475', 'Congenital bullous ichthyosiform erythroderma', 'XPO:0129582', 'increased size of the portion of organism substance', 0.42105263157894735, 5.972749669260594, 1.585825326448175, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(463656, 'HP:0007475', 'Congenital bullous ichthyosiform erythroderma', 'XPO:0130896', 'increased size of the skin seromucous gland', 0.41379310344827586, 7.420886955069779, 1.752344670285258, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(463657, 'HP:0007475', 'Congenital bullous ichthyosiform erythroderma', 'XPO:0102626', 'abnormal granular gland morphology', 0.40384615384615385, 7.420886955069779, 1.7311547172139254, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(463658, 'HP:0007475', 'Congenital bullous ichthyosiform erythroderma', 'XPO:0102727', 'abnormal skin seromucous gland morphology', 0.40384615384615385, 7.420886955069779, 1.7311547172139254, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(463659, 'HP:0007475', 'Congenital bullous ichthyosiform erythroderma', 'XPO:0130706', 'increased size of the stratum spongiosum', 0.42105263157894735, 7.420886955069779, 1.7676492811307372, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(463660, 'HP:0007475', 'Congenital bullous ichthyosiform erythroderma', 'XPO:0102561', 'abnormal dermis morphology', 0.4117647058823529, 7.420886955069779, 1.7480444314835069, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(463661, 'HP:0007475', 'Congenital bullous ichthyosiform erythroderma', 'XPO:0129655', 'increased size of the skin', 0.46296296296296297, 11.09310877090129, 2.26620795714932, 'UPHENO:0081431', 'abnormal skin of body morphology in the independent continuant'),
(463662, 'HP:0007475', 'Congenital bullous ichthyosiform erythroderma', 'XPO:0130126', 'increased size of the stratum compactum', 0.42105263157894735, 7.420886955069779, 1.7676492811307372, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(463663, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100546', 'abnormal whole organism', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463664, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0115512', 'abnormally semi-erect whole organism', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463665, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0107278', 'abnormal medial region', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463666, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100032', 'abnormal nervous system', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(463667, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0141715', 'abnormal septum', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463668, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0101519', 'abnormal hypobranchial placode', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463669, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100103', 'abnormal trunk', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463670, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100437', 'abnormal proepicardium', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(463671, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0107270', 'abnormal proximal-distal axis', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463672, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0101110', 'abnormal cell-free extract', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463673, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100781', 'abnormal presumptive ectoderm', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463674, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0131687', 'abnormal astral microtubule', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(463675, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100626', 'abnormal primordial germ cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(463676, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100784', 'abnormal left blastomere', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(463677, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100120', 'abnormal genital system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(463678, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100643', 'abnormal thoracic region', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463679, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0101378', 'abnormal blastomere D1', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(463680, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0131669', 'abnormal Roux spot', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(463681, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0141748', 'abnormal gas homeostasis', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(463682, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100285', 'abnormal progenitor cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(463683, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100069', 'abnormal urinary system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(463684, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0142057', 'abnormal desmosome', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(463685, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100999', 'abnormal serous membrane', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463686, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100205', 'abnormal limb segment', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(463687, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0141775', 'abnormal nitrogen compound metabolic process', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(463688, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100887', 'abnormal right-dorsal blastomere', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(463689, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100612', 'abnormal unilaminar epithelium', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463690, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0101501', 'abnormal parabrachial area', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(463691, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0107312', 'abnormal filopodium', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(463692, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0107269', 'abnormal right side', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463693, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100854', 'abnormal spiracle', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463694, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0141264', 'abnormal schooling behavior', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(463695, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100239', 'abnormal acellular anatomical structure', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463696, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0107271', 'abnormal apical region', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463697, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100638', 'abnormal polar body', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(463698, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100549', 'abnormal mitotic cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(463699, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100135', 'abnormal surface structure', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463700, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100062', 'abnormal anatomical space', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463701, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100423', 'abnormal process', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463702, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100028', 'abnormal anatomical cluster', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463703, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0141499', 'abnormal tadpole', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463704, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0115509', 'abnormally semi-viable whole organism', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463705, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100277', 'abnormal blastocoel', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463706, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0141792', 'abnormal small molecule metabolic process', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(463707, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0141782', 'abnormal methylation', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(463708, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0142056', 'abnormal main body axis', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463709, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0101132', 'abnormal apoptotic cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(463710, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100372', 'abnormal hematological system', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(463711, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100827', 'abnormal atypical epithelium', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463712, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0101543', 'abnormal external gill', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(463713, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0141771', 'abnormal urea homeostasis', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(463714, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0141797', 'abnormal hydrogen metabolic process', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(463715, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100293', 'abnormal duct', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463716, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100956', 'abnormal centrosome', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(463717, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100394', 'abnormal marginal zone', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463718, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100392', 'abnormal cilium', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(463719, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100493', 'abnormal liver and biliary system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(463720, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100917', 'abnormal stage III oocyte', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(463721, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0101326', 'abnormal cementoblast', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(463722, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0107259', 'abnormal animal-vegetal axis', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463723, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0116494', 'absent biological process', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(463724, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0101072', 'abnormal mitochondrial cloud', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(463725, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100915', 'abnormal dermal system', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463726, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100816', 'abnormal blastocoel anlage', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463727, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100196', 'abnormal neuron', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(463728, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100745', 'abnormal anterior lymph sac', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(463729, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0101029', 'abnormal right spleen primordium', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(463730, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100218', 'abnormal epithelial cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(463731, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0115391', 'abnormally undifferentiated alimentary system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(463732, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100551', 'abnormal oocyte cortex', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(463733, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100025', 'abnormal oocyte', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(463734, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0101241', 'abnormal nucleate erythrocyte', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(463735, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100991', 'abnormal iliac process primordium', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463736, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0107267', 'abnormal ventral side', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463737, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0101157', 'abnormal female organism', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463738, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0101362', 'abnormal vegetal cortex', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(463739, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0141796', 'abnormal demethylation', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(463740, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100386', 'abnormal limb', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(463741, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0131677', 'abnormal actin filament', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(463742, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100585', 'abnormal elastica externa', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(463743, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100416', 'abnormal ligament', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(463744, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0131675', 'abnormal spindle microtubule', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(463745, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0101004', 'abnormal acid secreting cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(463746, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100627', 'abnormal pharyngeal region', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(463747, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100856', 'abnormal simple organ', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463748, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0107263', 'abnormal anatomical side', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463749, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100289', 'abnormal chondroblast', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(463750, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100026', 'abnormal germ cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(463751, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100225', 'abnormal endocrine system', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(463752, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100994', 'abnormal granular gland', 0.4482758620689655, 6.4952303822948485, 1.7063572307578971, 'UPHENO:0002635', 'abnormal integument'),
(463753, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100108', 'abnormal cell part', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(463754, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100172', 'abnormal stem cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(463755, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100724', 'abnormal kinetochore', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(463756, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0101221', 'abnormal larval immune system', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(463757, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100429', 'abnormal spermatid', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(463758, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0115758', 'abnormally decreased mobility of melanoblast', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(463759, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0107261', 'abnormal dorsal-ventral axis', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463760, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0101529', 'abnormal skin mucous gland', 0.41935483870967744, 6.4952303822948485, 1.650395797785929, 'UPHENO:0002635', 'abnormal integument'),
(463761, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100006', 'abnormal anatomical structure', 0.5294117647058824, 1.706362323152461, 0.9504568842024205, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463762, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0107268', 'abnormal left side', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463763, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0101461', 'abnormal sperm entry point', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(463764, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0101467', 'abnormal alkali secreting cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(463765, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100547', 'abnormal blastomere V2', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(463766, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0101573', 'abnormal peripheral vegetal yolk mass', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463767, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0101208', 'abnormal stratum spongiosum', 0.41935483870967744, 6.4952303822948485, 1.650395797785929, 'UPHENO:0002635', 'abnormal integument'),
(463768, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100339', 'abnormal circumblastoporal collar', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463769, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0101071', 'abnormal endoplasmic reticulum', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(463770, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0141745', 'abnormal creatinine homeostasis', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(463771, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100449', 'abnormal lymphocyte', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(463772, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100515', 'abnormal somatic stem cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(463773, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0101713', 'abnormal anatomical entity in vitro morphology', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463774, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0101240', 'abnormal ciliated non-epidermal cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(463775, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0107265', 'abnormal posterior side', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463776, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100791', 'abnormal multiciliated cell precursor', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(463777, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100458', 'abnormal autopod', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(463778, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0101389', 'abnormal wedge region', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(463779, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0141790', 'abnormal cellular metabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(463780, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0101322', 'abnormal iridophore', 0.40625, 6.4952303822948485, 1.624403688375301, 'HP:0001574', 'Abnormality of the integument'),
(463781, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100667', 'abnormal vegetal yolk mass', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463782, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0116434', 'abnormal biological process', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(463783, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100010', 'abnormal multicellular anatomical structure', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463784, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100762', 'abnormal intersomitic region', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463785, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0115505', 'dead whole organism', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463786, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100544', 'abnormal neuromast support cell', 0.41935483870967744, 6.4952303822948485, 1.650395797785929, 'HP:0001574', 'Abnormality of the integument'),
(463787, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100337', 'abnormal zygote', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(463788, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0141841', 'abnormality of whole organism mass', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(463789, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0101302', 'abnormal subcortical cytoplasm', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(463790, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100890', 'abnormal pharyngeal cavity', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(463791, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0141794', 'abnormal prosthetic group metabolic process', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(463792, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100258', 'abnormal organ part', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463793, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0101503', 'abnormal organ cortex', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463794, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0101373', 'abnormal oxygen accumulating cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(463795, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0141781', 'abnormal secondary metabolic process', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(463796, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0107288', 'abnormal larval alimentary system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(463797, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100158', 'abnormal neuromere', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(463798, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0101212', 'abnormal glomeral mesenchyme', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(463799, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0101061', 'abnormal plasma membrane', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(463800, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100151', 'abnormal primordium', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463801, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0101575', 'abnormal vitelline membrane', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(463802, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0141860', 'abnormal malate-aspartate shuttle', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(463803, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100133', 'abnormal solid compound organ', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463804, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0141770', 'abnormal urate homeostasis', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(463805, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0107264', 'abnormal anterior side', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463806, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0101450', 'abnormal myeloid cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(463807, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100843', 'abnormal fasciculated network of fibrils', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(463808, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100273', 'abnormal visual system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(463809, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0101424', 'abnormal coelomic epithelium', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463810, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0107266', 'abnormal dorsal side', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463811, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0101498', 'abnormal stage II oocyte', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(463812, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0107272', 'abnormal axial region', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463813, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100665', 'abnormal egg jelly', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463814, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0141787', 'abnormal hormone metabolic process', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(463815, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0101411', 'abnormal marginal zone (sensu neural)', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463816, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100537', 'abnormal medium cavity', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(463817, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100481', 'abnormal anatomical line', 0.5294117647058824, 1.706362323152461, 0.9504568842024205, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463818, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100164', 'abnormal neural nucleus', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(463819, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0101366', 'abnormal morula cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(463820, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0107253', 'abnormal enteric nervous system', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(463821, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0107258', 'abnormal anatomical axis', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463822, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100545', 'abnormal male organism', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463823, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0101472', 'abnormal zygote cortex', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(463824, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0101200', 'abnormal joint region', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463825, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0101095', 'abnormal skin seromucous gland', 0.4482758620689655, 6.4952303822948485, 1.7063572307578971, 'UPHENO:0002635', 'abnormal integument'),
(463826, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100531', 'abnormal proliferative region', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463827, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100207', 'abnormal blastema', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463828, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0141271', 'increased surface breathing', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(463829, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100989', 'abnormal right blastomere', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(463830, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100935', 'abnormal skeleton', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(463831, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0101560', 'abnormal compound organ component', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463832, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:00000000', 'Xenopus phenotype', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(463833, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100610', 'abnormal appendage', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463834, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100802', 'abnormal exocrine cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(463835, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100846', 'abnormal hindlimb', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(463836, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0141263', 'abnormal visually guided collision avoidance behavior', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(463837, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100152', 'abnormal alimentary system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(463838, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0107311', 'abnormal apical junction complex', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(463839, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0107285', 'abnormal flexural organ', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(463840, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100465', 'abnormal skeletal system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(463841, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100084', 'abnormal anatomical group', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463842, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0101228', 'abnormal mesenchymal stem cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(463843, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100721', 'abnormal centromere', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(463844, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0101010', 'abnormal dorsal marginal zone', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463845, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0102113', 'abnormal anatomical line morphology', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463846, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100894', 'abnormal nucleus', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(463847, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100308', 'abnormal early embryonic cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(463848, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0101406', 'abnormal cleavage furrow', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463849, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100104', 'abnormal embryonic structure', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463850, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100317', 'abnormal respiratory system', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(463851, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0101387', 'abnormal melanophore', 0.40625, 6.4952303822948485, 1.624403688375301, 'HP:0001574', 'Abnormality of the integument'),
(463852, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0141743', 'abnormal chemical homeostasis within a tissue', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(463853, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100728', 'abnormal cell condensation', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463854, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0107276', 'abnormal dorsal region', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463855, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100484', 'abnormal cement gland primordium', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463856, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0101078', 'abnormal mucous gland', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463857, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100862', 'abnormal blastomere V1', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(463858, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0101278', 'abnormal pigment cell', 0.41935483870967744, 6.4952303822948485, 1.650395797785929, 'HP:0001574', 'Abnormality of the integument'),
(463859, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100377', 'abnormal connective tissue', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(463860, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100912', 'abnormal trabecula', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463861, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100251', 'abnormal proteinaceous extracellular matrix', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463862, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0101113', 'abnormal stage IV oocyte', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(463863, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0101283', 'abnormal left-ventral blastomere', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(463864, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100969', 'abnormal disaggregated/reaggregated ectoderm treated with activin', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463865, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0141718', 'abnormal posterior notochord', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(463866, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100203', 'abnormal endocrine cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(463867, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100823', 'abnormal blood', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(463868, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0101333', 'abnormal barrier epithelial cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(463869, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100307', 'abnormal blastomere', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(463870, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0101347', 'abnormal hindlimb region', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463871, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0101023', 'abnormal ultimobranchial body', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(463872, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100114', 'abnormal peripheral nervous system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(463873, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100295', 'abnormal extracellular matrix', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463874, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100231', 'abnormal compound organ', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463875, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0101553', 'abnormal dental epithelium', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463876, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100976', 'abnormal multiciliated cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(463877, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0101040', 'abnormal axial mesoderm', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463878, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100002', 'abnormal head', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(463879, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100800', 'abnormal ventral marginal zone', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463880, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0131666', 'abnormal adherens junction', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(463881, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100688', 'abnormal adipose tissue', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(463882, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100403', 'abnormal forelimb', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(463883, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0101591', 'abnormal xanthophore', 0.40625, 6.4952303822948485, 1.624403688375301, 'HP:0001574', 'Abnormality of the integument'),
(463884, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0131691', 'abnormal molecular function', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(463885, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0101497', 'abnormal ciliary axoneme', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(463886, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100477', 'abnormal pericyte', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(463887, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0101638', 'abnormal anatomical structure morphology', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463888, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0141778', 'abnormal biosynthetic process', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(463889, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100653', 'abnormal myoblast', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(463890, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0101515', 'abnormal neuromast mantle cell', 0.41935483870967744, 6.4952303822948485, 1.650395797785929, 'HP:0001574', 'Abnormality of the integument'),
(463891, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0101098', 'abnormal mineralized extracellular matrix', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463892, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0141266', 'abnormal surface breathing', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(463893, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0101176', 'abnormal non-ciliated epithelial cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(463894, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100009', 'abnormal multi-tissue structure', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463895, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100383', 'abnormal amputated fin', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463896, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100796', 'abnormal pseudoblastema', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463897, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0142054', 'abnormal digestive tract', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(463898, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100742', 'abnormal musculoskeletal system', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463899, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100384', 'abnormal amputated tissue', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463900, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0131723', 'abnormal pathway-restricted SMAD protein phosphorylation', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(463901, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0101074', 'abnormal germinal vesicle', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(463902, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100983', 'abnormal skin gland', 0.4642857142857143, 6.4952303822948485, 1.7365605884892232, 'UPHENO:0002635', 'abnormal integument'),
(463903, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0107273', 'abnormal basal region', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463904, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0101569', 'abnormal activin-induced ectoderm', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463905, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100202', 'abnormal embryo', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463906, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100256', 'abnormal paired appendage', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463907, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100393', 'abnormal involuting marginal zone', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463908, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100282', 'abnormal pelvic girdle primordium', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463909, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0101237', 'abnormal mucus secreting cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(463910, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100422', 'abnormal notochord', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(463911, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100402', 'abnormal zeugopod', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(463912, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100482', 'abnormal Mullerian duct', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(463913, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100201', 'abnormal cavitated compound organ', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463914, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100858', 'abnormal presumptive midbrain-hindbrain boundary', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(463915, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100031', 'abnormal central nervous system', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(463916, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0101435', 'abnormal paracrine cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(463917, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100363', 'abnormal cardiovascular system', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463918, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100581', 'abnormal immune system', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(463919, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100162', 'abnormal presumptive rhombomere', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463920, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0101254', 'abnormal stratum compactum', 0.41935483870967744, 6.4952303822948485, 1.650395797785929, 'HP:0001574', 'Abnormality of the integument'),
(463921, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0107339', 'abnormal yolk platelet', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(463922, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0141786', 'abnormal pigment metabolic process', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(463923, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100067', 'abnormal animal hemisphere', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463924, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100427', 'abnormal olfactory system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(463925, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100468', 'abnormal muscular system', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463926, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0101297', 'abnormal barrier cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(463927, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100557', 'abnormal prime meridian', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463928, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0141783', 'abnormal collagen metabolic process', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(463929, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100023', 'abnormal mesenchyme', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463930, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100003', 'abnormal organism subdivision', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463931, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0107260', 'abnormal anterior-posterior axis', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463932, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100642', 'abnormal gustatory system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(463933, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0101149', 'abnormal amputated limb', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463934, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0101535', 'abnormal absorptive cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(463935, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100691', 'abnormal keratin accumulating cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(463936, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0101480', 'abnormal stage V oocyte', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(463937, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100533', 'abnormal melanoblast', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(463938, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100014', 'abnormal tissue', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463939, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100232', 'abnormal lymphatic system', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(463940, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0107262', 'abnormal left-right axis', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463941, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0115508', 'abnormally peramorphic growth of whole organism', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463942, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0101463', 'abnormal right-ventral blastomere', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(463943, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100186', 'abnormal uveal tract', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463944, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0141265', 'abnormal escape behavior', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(463945, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100587', 'abnormal vestibuloauditory system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(463946, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100309', 'abnormal vegetal hemisphere', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463947, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100268', 'abnormal circulatory system', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463948, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100786', 'abnormal presumptive axial mesoderm', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463949, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100070', 'abnormal anatomical system', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463950, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100553', 'abnormal laryngeal muscle primordium', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463951, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100704', 'abnormal Merkel cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(463952, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0141784', 'abnormal cellular hormone metabolic process', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(463953, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100842', 'abnormal left-dorsal blastomere', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(463954, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0101570', 'abnormal forelimb region', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463955, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0101224', 'abnormal dorsal involuting marginal zone', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463956, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0101448', 'abnormal myelin accumulating cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(463957, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100754', 'abnormal electrically active cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(463958, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100503', 'abnormal blastomere D2', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(463959, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0101099', 'abnormal ventro-lateral marginal zone', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463960, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0131725', 'abnormal phosphorylation of RNA polymerase II C-terminal domain', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(463961, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0141776', 'abnormal metabolic process', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(463962, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0101587', 'abnormal hemangioblast', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(463963, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0142051', 'abnormal cerebrospinal fluid', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(463964, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0141497', 'abnormal lymphoblast', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(463965, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0131667', 'abnormal actin cytoskeleton', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(463966, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100902', 'abnormal spermatocyte', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(463967, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100507', 'abnormal skin', 0.48148148148148145, 6.4952303822948485, 1.7684267434730943, 'HP:0001574', 'Abnormality of the integument'),
(463968, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0141904', 'abnormal glucosamine metabolic process', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(463969, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100574', 'abnormal gastrula cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(463970, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100378', 'abnormal perichondrium', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(463971, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0101451', 'abnormal dorsal lymph space', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(463972, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100852', 'abnormal interdigital region', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(463973, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100868', 'abnormal transporting epithelium', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463974, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100444', 'abnormal cement gland', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463975, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100296', 'abnormal tail region', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463976, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100916', 'abnormal principal cavity', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(463977, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0101168', 'abnormal circulating cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(463978, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100249', 'abnormal avascular GAG-rich matrix', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463979, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0141714', 'abnormal anterior notochord', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(463980, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0101109', 'abnormal egg cell-free extract', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463981, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0101311', 'abnormal bottle cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(463982, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100501', 'abnormal urogenital system', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(463983, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0141276', 'decreased surface breathing', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(463984, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100722', 'abnormal barbel', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463985, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100929', 'abnormal dermis', 0.4482758620689655, 6.4952303822948485, 1.7063572307578971, 'HP:0001574', 'Abnormality of the integument'),
(463986, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0141267', 'abnormal resting posture', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(463987, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0101349', 'abnormal trunk region', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463988, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0101577', 'abnormal notochordal epithelium', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463989, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100727', 'abnormal odontogenic papilla', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(463990, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0101547', 'abnormal lampbrush chromosome', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(463991, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100605', 'abnormal prechordal plate', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463992, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100344', 'abnormal portion of organism substance', 0.5294117647058824, 1.706362323152461, 0.9504568842024205, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463993, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0101264', 'abnormal mitotic spindle', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(463994, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0141315', 'abnormal anatomical region', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(463995, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100702', 'abnormal glial cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(463996, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100176', 'abnormal stage VI oocyte', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(463997, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100417', 'abnormal dense regular connective tissue', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(463998, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0101468', 'abnormal stage I oocyte', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(463999, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100509', 'abnormal germ plasm', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(464000, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0101136', 'abnormal ooplasm', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(464001, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100274', 'abnormal sensory system', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(464002, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0101313', 'abnormal Eberth-Kastschenko layer', 0.41935483870967744, 6.4952303822948485, 1.650395797785929, 'HP:0001574', 'Abnormality of the integument'),
(464003, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100807', 'abnormal matrix-based tissue', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(464004, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100707', 'abnormal central vegetal yolk mass', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(464005, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100588', 'abnormal unicellular gland', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(464006, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0142052', 'abnormal nasal region', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(464007, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0131685', 'abnormal cortical actin cytoskeleton', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(464008, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0101096', 'abnormal tendon', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(464009, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100715', 'abnormal ciliated cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(464010, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0101405', 'abnormal ring structure', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(464011, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0101107', 'abnormal erythroid cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(464012, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100900', 'abnormal angioblast', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(464013, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100415', 'abnormal secretory epithelial cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(464014, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0141777', 'abnormal catabolic process', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(464015, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0101141', 'abnormal Keller explant', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(464016, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100081', 'abnormal anatomical entity in vitro', 0.5294117647058824, 1.706362323152461, 0.9504568842024205, 'UPHENO:0002536', 'abnormal anatomical entity'),
(464017, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0101976', 'abnormal portion of organism substance morphology', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(464018, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0141791', 'abnormal primary metabolic process', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(464019, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0107284', 'abnormal migrating myoblast', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(464020, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100913', 'abnormal Brachets cleft', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(464021, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0101092', 'abnormal dorso-lateral marginal zone', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(464022, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0101409', 'abnormal perivitelline space', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(464023, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0141272', 'absent surface breathing', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(464024, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0101513', 'abnormal basal body', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(464025, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100175', 'abnormal migrating neuroblast', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(464026, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100511', 'abnormal stylopod', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(464027, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100192', 'abnormal epithelium', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(464028, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100261', 'abnormal multilaminar epithelium', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(464029, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100899', 'abnormal secondary spermatogonium', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(464030, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100888', 'abnormal microtubule', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(464031, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100599', 'abnormal adult immune system', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(464032, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100674', 'abnormal secondary oogonium', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(464033, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100060', 'abnormal regenerating tissue', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(464034, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100640', 'abnormal notochordal sheath', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(464035, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0101174', 'abnormal articular system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(464036, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100004', 'abnormal cell', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(464037, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100573', 'abnormal extraembryonic structure', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(464038, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100907', 'abnormal cytoplasm', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(464039, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0141772', 'abnormal water homeostasis', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(464040, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0141738', 'abnormal carbon dioxide homeostasis', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(464041, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0101220', 'abnormal centriole', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(464042, 'HP:0007451', 'Ipsilateral lack of facial sweating', 'XPO:0100265', 'abnormal sensory epithelial cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(464043, 'HP:0007187', 'Focal lissencephaly', 'XPO:0101797', 'abnormal lateral pallium morphology', 0.4084507042253521, 8.02346099791745, 1.810300608993995, 'HP:0002060', 'Abnormal cerebral morphology'),
(464044, 'HP:0007187', 'Focal lissencephaly', 'XPO:0100195', 'abnormal retromammillary area', 0.40298507462686567, 6.667568321314008, 1.639185931352649, 'HP:0100547', 'Abnormal forebrain morphology'),
(464045, 'HP:0007187', 'Focal lissencephaly', 'XPO:0102191', 'abnormal telencephalon morphology', 0.42028985507246375, 8.02346099791745, 1.8363494384224073, 'HP:0002060', 'Abnormal cerebral morphology'),
(464046, 'HP:0007187', 'Focal lissencephaly', 'XPO:0102442', 'abnormal medial pallium morphology', 0.4084507042253521, 8.02346099791745, 1.810300608993995, 'HP:0002060', 'Abnormal cerebral morphology'),
(464047, 'HP:0007187', 'Focal lissencephaly', 'XPO:0100590', 'abnormal hypothalamus', 0.4090909090909091, 6.667568321314008, 1.6515573214369805, 'HP:0100547', 'Abnormal forebrain morphology'),
(464048, 'HP:0007187', 'Focal lissencephaly', 'XPO:0102066', 'abnormal ventral pallium morphology', 0.4084507042253521, 8.02346099791745, 1.810300608993995, 'HP:0002060', 'Abnormal cerebral morphology'),
(464049, 'HP:0007187', 'Focal lissencephaly', 'XPO:0100263', 'abnormal prethalamus', 0.40298507462686567, 6.667568321314008, 1.639185931352649, 'HP:0100547', 'Abnormal forebrain morphology'),
(464050, 'HP:0007187', 'Focal lissencephaly', 'XPO:0102826', 'abnormal anterior commissure morphology', 0.4084507042253521, 8.02346099791745, 1.810300608993995, 'HP:0002060', 'Abnormal cerebral morphology'),
(464051, 'HP:0007187', 'Focal lissencephaly', 'XPO:0103178', 'abnormal dorsal pallium morphology', 0.4084507042253521, 8.02346099791745, 1.810300608993995, 'HP:0002060', 'Abnormal cerebral morphology'),
(464052, 'HP:0007187', 'Focal lissencephaly', 'XPO:0101186', 'abnormal optic chiasm', 0.4090909090909091, 6.667568321314008, 1.6515573214369805, 'HP:0100547', 'Abnormal forebrain morphology'),
(464053, 'HP:0007187', 'Focal lissencephaly', 'XPO:0102968', 'abnormal medial ganglionic eminence morphology', 0.4027777777777778, 8.02346099791745, 1.7976851200440698, 'HP:0002060', 'Abnormal cerebral morphology'),
(464054, 'HP:0007187', 'Focal lissencephaly', 'XPO:0101496', 'abnormal subcommissural organ', 0.40298507462686567, 6.667568321314008, 1.639185931352649, 'HP:0100547', 'Abnormal forebrain morphology'),
(464055, 'HP:0007187', 'Focal lissencephaly', 'XPO:0102357', 'abnormal subpallium morphology', 0.4142857142857143, 8.02346099791745, 1.8231854734408677, 'HP:0002060', 'Abnormal cerebral morphology'),
(464056, 'HP:0007187', 'Focal lissencephaly', 'XPO:0100575', 'abnormal diencephalon', 0.4153846153846154, 6.667568321314008, 1.6642131181731699, 'HP:0100547', 'Abnormal forebrain morphology'),
(464057, 'HP:0007187', 'Focal lissencephaly', 'XPO:0100962', 'abnormal dorsal thalamus', 0.40298507462686567, 6.667568321314008, 1.639185931352649, 'HP:0100547', 'Abnormal forebrain morphology'),
(464058, 'HP:0007187', 'Focal lissencephaly', 'XPO:0100695', 'abnormal zona limitans intrathalamica', 0.40298507462686567, 6.667568321314008, 1.639185931352649, 'HP:0100547', 'Abnormal forebrain morphology'),
(464059, 'HP:0007187', 'Focal lissencephaly', 'XPO:0101986', 'abnormal amygdala morphology', 0.4027777777777778, 8.02346099791745, 1.7976851200440698, 'HP:0002060', 'Abnormal cerebral morphology'),
(464060, 'HP:0007187', 'Focal lissencephaly', 'XPO:0101851', 'abnormal basal ganglion morphology', 0.4027777777777778, 8.02346099791745, 1.7976851200440698, 'HP:0002060', 'Abnormal cerebral morphology'),
(464061, 'HP:0007187', 'Focal lissencephaly', 'XPO:0100763', 'abnormal pretectum', 0.4090909090909091, 6.667568321314008, 1.6515573214369805, 'HP:0100547', 'Abnormal forebrain morphology'),
(464062, 'HP:0007187', 'Focal lissencephaly', 'XPO:0102007', 'abnormal anterior entopeduncular region morphology', 0.4264705882352941, 8.02346099791745, 1.8498027277157947, 'HP:0002060', 'Abnormal cerebral morphology'),
(464063, 'HP:0007187', 'Focal lissencephaly', 'XPO:0102238', 'abnormal basal forebrain morphology', 0.4142857142857143, 8.02346099791745, 1.8231854734408677, 'HP:0002060', 'Abnormal cerebral morphology'),
(464064, 'HP:0007187', 'Focal lissencephaly', 'XPO:0101293', 'abnormal posterior hypothalamus', 0.40298507462686567, 6.667568321314008, 1.639185931352649, 'HP:0100547', 'Abnormal forebrain morphology'),
(464065, 'HP:0007187', 'Focal lissencephaly', 'XPO:0101970', 'abnormal lateral ganglionic eminence morphology', 0.4027777777777778, 8.02346099791745, 1.7976851200440698, 'HP:0002060', 'Abnormal cerebral morphology'),
(464066, 'HP:0007187', 'Focal lissencephaly', 'XPO:0100157', 'abnormal optic tract', 0.4090909090909091, 6.667568321314008, 1.6515573214369805, 'HP:0100547', 'Abnormal forebrain morphology'),
(464067, 'HP:0007187', 'Focal lissencephaly', 'XPO:0100729', 'abnormal thalamus', 0.4090909090909091, 6.667568321314008, 1.6515573214369805, 'HP:0100547', 'Abnormal forebrain morphology'),
(464068, 'HP:0007187', 'Focal lissencephaly', 'XPO:0140421', 'abnormally necrotic anterior entopeduncular region', 0.4084507042253521, 8.02346099791745, 1.810300608993995, 'HP:0002060', 'Abnormal cerebral morphology'),
(464069, 'HP:0007187', 'Focal lissencephaly', 'XPO:0102174', 'abnormal pallium morphology', 0.4142857142857143, 8.02346099791745, 1.8231854734408677, 'HP:0002060', 'Abnormal cerebral morphology'),
(464070, 'HP:0007187', 'Focal lissencephaly', 'XPO:0101354', 'abnormal eminentia thalami', 0.4090909090909091, 6.667568321314008, 1.6515573214369805, 'HP:0100547', 'Abnormal forebrain morphology'),
(464071, 'HP:0007187', 'Focal lissencephaly', 'XPO:0101053', 'abnormal anterior hypothalamus', 0.40298507462686567, 6.667568321314008, 1.639185931352649, 'HP:0100547', 'Abnormal forebrain morphology'),
(464072, 'HP:0007187', 'Focal lissencephaly', 'XPO:0107380', 'abnormal dorsal telencephalon morphology', 0.4142857142857143, 8.02346099791745, 1.8231854734408677, 'HP:0002060', 'Abnormal cerebral morphology'),
(464073, 'HP:0033257', 'Delayed ability to walk with support', 'XPO:0100427', 'abnormal olfactory system', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(464074, 'HP:0033257', 'Delayed ability to walk with support', 'XPO:0142051', 'abnormal cerebrospinal fluid', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(464075, 'HP:0033257', 'Delayed ability to walk with support', 'XPO:0100274', 'abnormal sensory system', 0.43333333333333335, 3.94131651835137, 1.3068679445984308, 'UPHENO:0004523', 'abnormal nervous system'),
(464076, 'HP:0033257', 'Delayed ability to walk with support', 'XPO:0100032', 'abnormal nervous system', 0.4482758620689655, 3.94131651835137, 1.3292091859262085, 'UPHENO:0004523', 'abnormal nervous system'),
(464077, 'HP:0033257', 'Delayed ability to walk with support', 'XPO:0100642', 'abnormal gustatory system', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(464078, 'HP:0033257', 'Delayed ability to walk with support', 'XPO:0100587', 'abnormal vestibuloauditory system', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(464079, 'HP:0033257', 'Delayed ability to walk with support', 'XPO:0100114', 'abnormal peripheral nervous system', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(464080, 'HP:0033257', 'Delayed ability to walk with support', 'XPO:0100164', 'abnormal neural nucleus', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(464081, 'HP:0033257', 'Delayed ability to walk with support', 'XPO:0100273', 'abnormal visual system', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(464082, 'HP:0033257', 'Delayed ability to walk with support', 'XPO:0100031', 'abnormal central nervous system', 0.43333333333333335, 3.94131651835137, 1.3068679445984308, 'UPHENO:0004523', 'abnormal nervous system'),
(464083, 'HP:0033257', 'Delayed ability to walk with support', 'XPO:0107253', 'abnormal enteric nervous system', 0.43333333333333335, 3.94131651835137, 1.3068679445984308, 'UPHENO:0004523', 'abnormal nervous system'),
(464084, 'HP:0011199', 'EEG with generalized sharp slow waves', 'XPO:0100274', 'abnormal sensory system', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(464085, 'HP:0011199', 'EEG with generalized sharp slow waves', 'XPO:0100031', 'abnormal central nervous system', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(464086, 'HP:0011199', 'EEG with generalized sharp slow waves', 'XPO:0107253', 'abnormal enteric nervous system', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(464087, 'HP:0011199', 'EEG with generalized sharp slow waves', 'XPO:0100032', 'abnormal nervous system', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(464088, 'HP:0009985', 'Duplication of phalanx of 5th finger', 'XPO:0103467', 'bifurcated forelimb digit 4', 0.40869565217391307, 7.492661022682715, 1.7499194219115835, 'HP:0001167', 'Abnormal finger morphology'),
(464089, 'HP:0009985', 'Duplication of phalanx of 5th finger', 'XPO:0133358', 'fused forelimb digits', 0.44761904761904764, 7.492661022682715, 1.8313540867635612, 'HP:0001167', 'Abnormal finger morphology'),
(464090, 'HP:0009985', 'Duplication of phalanx of 5th finger', 'XPO:0102880', 'abnormal digit-joint region morphology', 0.40963855421686746, 6.466375519622663, 1.6275370099882747, 'UPHENO:0086700', 'abnormal digit morphology'),
(464091, 'HP:0009985', 'Duplication of phalanx of 5th finger', 'XPO:0115786', 'duplicated forelimb digit 2 in regenerating forelimb', 0.5128205128205128, 11.430690130100139, 2.4211345221631793, 'HP:0009997', 'Duplication of phalanx of hand'),
(464092, 'HP:0009985', 'Duplication of phalanx of 5th finger', 'XPO:0140716', 'abnormally necrotic forelimb digit 4', 0.4392523364485981, 7.492661022682715, 1.8141578929163595, 'HP:0001167', 'Abnormal finger morphology'),
(464093, 'HP:0009985', 'Duplication of phalanx of 5th finger', 'XPO:0129652', 'increased size of the forelimb digit 3', 0.43119266055045874, 7.492661022682715, 1.7974371869340195, 'HP:0001167', 'Abnormal finger morphology'),
(464094, 'HP:0009985', 'Duplication of phalanx of 5th finger', 'XPO:0128172', 'decreased size of the forelimb digit 3', 0.42727272727272725, 7.492661022682715, 1.7892483644513149, 'HP:0001167', 'Abnormal finger morphology'),
(464095, 'HP:0009985', 'Duplication of phalanx of 5th finger', 'XPO:0115788', 'duplicated forelimb digit 4 in regenerating forelimb', 0.5128205128205128, 11.430690130100139, 2.4211345221631793, 'HP:0009997', 'Duplication of phalanx of hand'),
(464096, 'HP:0009985', 'Duplication of phalanx of 5th finger', 'XPO:0130664', 'increased size of the forelimb digit 2', 0.43119266055045874, 7.492661022682715, 1.7974371869340195, 'HP:0001167', 'Abnormal finger morphology'),
(464097, 'HP:0009985', 'Duplication of phalanx of 5th finger', 'XPO:0130637', 'increased size of the forelimb digit 5', 0.43119266055045874, 7.492661022682715, 1.7974371869340195, 'HP:0001167', 'Abnormal finger morphology'),
(464098, 'HP:0009985', 'Duplication of phalanx of 5th finger', 'XPO:0102529', 'abnormal forelimb digit 4 morphology', 0.47959183673469385, 7.492661022682715, 1.8956315733546045, 'HP:0001167', 'Abnormal finger morphology'),
(464099, 'HP:0009985', 'Duplication of phalanx of 5th finger', 'XPO:0102598', 'abnormal forelimb digit 3 morphology', 0.47959183673469385, 7.492661022682715, 1.8956315733546045, 'HP:0001167', 'Abnormal finger morphology'),
(464100, 'HP:0009985', 'Duplication of phalanx of 5th finger', 'XPO:0103779', 'decreased size of the forelimb digit in the regenerating forelimb', 0.41228070175438597, 7.492661022682715, 1.7575777491876043, 'HP:0001167', 'Abnormal finger morphology'),
(464101, 'HP:0009985', 'Duplication of phalanx of 5th finger', 'XPO:0103466', 'bifurcated forelimb digit 3', 0.40869565217391307, 7.492661022682715, 1.7499194219115835, 'HP:0001167', 'Abnormal finger morphology'),
(464102, 'HP:0009985', 'Duplication of phalanx of 5th finger', 'XPO:0102787', 'abnormal forelimb digit 5 morphology', 0.47959183673469385, 7.492661022682715, 1.8956315733546045, 'HP:0001167', 'Abnormal finger morphology'),
(464103, 'HP:0009985', 'Duplication of phalanx of 5th finger', 'XPO:0102746', 'abnormal forelimb digit 2 morphology', 0.47959183673469385, 7.492661022682715, 1.8956315733546045, 'HP:0001167', 'Abnormal finger morphology'),
(464104, 'HP:0009985', 'Duplication of phalanx of 5th finger', 'XPO:0129161', 'decreased size of the forelimb digit 5', 0.42727272727272725, 7.492661022682715, 1.7892483644513149, 'HP:0001167', 'Abnormal finger morphology'),
(464105, 'HP:0009985', 'Duplication of phalanx of 5th finger', 'XPO:0141108', 'abnormally necrotic forelimb digit 2', 0.4392523364485981, 7.492661022682715, 1.8141578929163595, 'HP:0001167', 'Abnormal finger morphology'),
(464106, 'HP:0009985', 'Duplication of phalanx of 5th finger', 'XPO:0141556', 'abnormal forelimb digit morphology in the regenerating forelimb', 0.46078431372549017, 7.492661022682715, 1.8580905971761936, 'HP:0001167', 'Abnormal finger morphology'),
(464107, 'HP:0009985', 'Duplication of phalanx of 5th finger', 'XPO:0141143', 'abnormally necrotic forelimb digit 3', 0.4392523364485981, 7.492661022682715, 1.8141578929163595, 'HP:0001167', 'Abnormal finger morphology'),
(464108, 'HP:0009985', 'Duplication of phalanx of 5th finger', 'XPO:0103609', 'abnormally increased number of forelimb digit in the regenerating forelimb', 0.5357142857142857, 11.430690130100139, 2.4745876420664374, 'HP:0009997', 'Duplication of phalanx of hand'),
(464109, 'HP:0009985', 'Duplication of phalanx of 5th finger', 'XPO:0103468', 'bifurcated forelimb digit 5', 0.40869565217391307, 7.492661022682715, 1.7499194219115835, 'HP:0001167', 'Abnormal finger morphology'),
(464110, 'HP:0009985', 'Duplication of phalanx of 5th finger', 'XPO:0103755', 'increased size of the forelimb digit', 0.44339622641509435, 7.492661022682715, 1.822695153684504, 'HP:0001167', 'Abnormal finger morphology'),
(464111, 'HP:0009985', 'Duplication of phalanx of 5th finger', 'XPO:0129188', 'decreased size of the forelimb digit 2', 0.42727272727272725, 7.492661022682715, 1.7892483644513149, 'HP:0001167', 'Abnormal finger morphology'),
(464112, 'HP:0009985', 'Duplication of phalanx of 5th finger', 'XPO:0101810', 'abnormal digit morphology', 0.40963855421686746, 6.466375519622663, 1.6275370099882747, 'UPHENO:0086700', 'abnormal digit morphology'),
(464113, 'HP:0009985', 'Duplication of phalanx of 5th finger', 'XPO:0103634', 'abnormally increased number of forelimb digit', 0.5660377358490566, 11.430690130100139, 2.543659167505356, 'HP:0009997', 'Duplication of phalanx of hand'),
(464114, 'HP:0009985', 'Duplication of phalanx of 5th finger', 'XPO:0103432', 'decreased size of the forelimb digit', 0.4392523364485981, 7.492661022682715, 1.8141578929163595, 'HP:0001167', 'Abnormal finger morphology'),
(464115, 'HP:0009985', 'Duplication of phalanx of 5th finger', 'XPO:0129148', 'decreased size of the forelimb digit 4', 0.42727272727272725, 7.492661022682715, 1.7892483644513149, 'HP:0001167', 'Abnormal finger morphology'),
(464116, 'HP:0009985', 'Duplication of phalanx of 5th finger', 'XPO:0102214', 'abnormal forelimb digit morphology', 0.4895833333333333, 7.492661022682715, 1.9152759485311108, 'HP:0001167', 'Abnormal finger morphology'),
(464117, 'HP:0009985', 'Duplication of phalanx of 5th finger', 'XPO:0140219', 'abnormally necrotic forelimb digit', 0.4519230769230769, 7.492661022682715, 1.8401376099934432, 'HP:0001167', 'Abnormal finger morphology'),
(464118, 'HP:0009985', 'Duplication of phalanx of 5th finger', 'XPO:0133378', 'fused forelimb digits part of regenerating forelimb', 0.41964285714285715, 7.492661022682715, 1.7732009697610411, 'HP:0001167', 'Abnormal finger morphology'),
(464119, 'HP:0009985', 'Duplication of phalanx of 5th finger', 'XPO:0140898', 'abnormally necrotic forelimb digit 5', 0.4392523364485981, 7.492661022682715, 1.8141578929163595, 'HP:0001167', 'Abnormal finger morphology'),
(464120, 'HP:0009985', 'Duplication of phalanx of 5th finger', 'XPO:0115789', 'duplicated forelimb digit 5 in regenerating forelimb', 0.5128205128205128, 11.430690130100139, 2.4211345221631793, 'HP:0009997', 'Duplication of phalanx of hand'),
(464121, 'HP:0009985', 'Duplication of phalanx of 5th finger', 'XPO:0130624', 'increased size of the forelimb digit 4', 0.43119266055045874, 7.492661022682715, 1.7974371869340195, 'HP:0001167', 'Abnormal finger morphology'),
(464122, 'HP:0009985', 'Duplication of phalanx of 5th finger', 'XPO:0103465', 'bifurcated forelimb digit 2', 0.40869565217391307, 7.492661022682715, 1.7499194219115835, 'HP:0001167', 'Abnormal finger morphology'),
(464123, 'HP:0009985', 'Duplication of phalanx of 5th finger', 'XPO:0115787', 'duplicated forelimb digit 3 in regenerating forelimb', 0.5128205128205128, 11.430690130100139, 2.4211345221631793, 'HP:0009997', 'Duplication of phalanx of hand'),
(464124, 'HP:0001140', 'Limbal dermoid', 'XPO:0102476', 'abnormal lens transitional zone morphology', 0.41975308641975306, 9.014833150514745, 1.9452516645636548, 'UPHENO:0021038', 'abnormal anterior segment of eyeball morphology'),
(464125, 'HP:0001140', 'Limbal dermoid', 'XPO:0140968', 'abnormally necrotic conjunctiva', 0.43373493975903615, 12.720196747295123, 2.348870743551279, 'HP:0000502', 'Abnormal conjunctiva morphology'),
(464126, 'HP:0001140', 'Limbal dermoid', 'XPO:0130736', 'increased size of the cornea', 0.4175824175824176, 10.582693223545188, 2.1021766388248797, 'UPHENO:0020998', 'abnormal cornea morphology'),
(464127, 'HP:0001140', 'Limbal dermoid', 'XPO:0102513', 'abnormal sclera morphology', 0.42857142857142855, 13.568193653850074, 2.4114186980622665, 'HP:0000591', 'Abnormal sclera morphology'),
(464128, 'HP:0001140', 'Limbal dermoid', 'XPO:0129260', 'decreased size of the cornea', 0.4175824175824176, 10.582693223545188, 2.1021766388248797, 'UPHENO:0020998', 'abnormal cornea morphology'),
(464129, 'HP:0001140', 'Limbal dermoid', 'XPO:0128178', 'decreased size of the conjunctiva', 0.4235294117647059, 12.720196747295123, 2.3210724775226708, 'HP:0000502', 'Abnormal conjunctiva morphology'),
(464130, 'HP:0001140', 'Limbal dermoid', 'XPO:0140218', 'abnormally necrotic sclera', 0.4024390243902439, 13.568193653850074, 2.3367435924365605, 'HP:0000591', 'Abnormal sclera morphology'),
(464131, 'HP:0001140', 'Limbal dermoid', 'XPO:0103048', 'abnormal cornea morphology', 0.4810126582278481, 10.582693223545188, 2.256193564095799, 'UPHENO:0020998', 'abnormal cornea morphology'),
(464132, 'HP:0001140', 'Limbal dermoid', 'XPO:0100371', 'abnormal hyaloid blood vessel', 0.44285714285714284, 6.887869297006056, 1.7465228647932265, 'HP:0012372', 'Abnormal eye morphology'),
(464133, 'HP:0001140', 'Limbal dermoid', 'XPO:0102550', 'abnormal lens morphology', 0.43037974683544306, 9.014833150514745, 1.969721200851099, 'UPHENO:0021038', 'abnormal anterior segment of eyeball morphology'),
(464134, 'HP:0001140', 'Limbal dermoid', 'XPO:0100779', 'abnormal optic choroid vascular plexus', 0.43661971830985913, 6.887869297006056, 1.734179792355427, 'HP:0012372', 'Abnormal eye morphology'),
(464135, 'HP:0001140', 'Limbal dermoid', 'XPO:0129658', 'increased size of the conjunctiva', 0.4235294117647059, 12.720196747295123, 2.3210724775226708, 'HP:0000502', 'Abnormal conjunctiva morphology'),
(464136, 'HP:0001140', 'Limbal dermoid', 'XPO:0102657', 'abnormal conjunctiva morphology', 0.46153846153846156, 12.720196747295123, 2.422985769090098, 'HP:0000502', 'Abnormal conjunctiva morphology'),
(464137, 'HP:0001140', 'Limbal dermoid', 'XPO:0140375', 'abnormally necrotic lens', 0.40476190476190477, 9.014833150514745, 1.910199213986099, 'UPHENO:0021038', 'abnormal anterior segment of eyeball morphology'),
(464138, 'HP:0001140', 'Limbal dermoid', 'XPO:0100710', 'abnormal hyaloid vein', 0.4305555555555556, 6.887869297006056, 1.7220947685207388, 'HP:0012372', 'Abnormal eye morphology'),
(464139, 'HP:0001140', 'Limbal dermoid', 'XPO:0141141', 'abnormally necrotic cornea', 0.4470588235294118, 10.582693223545188, 2.1751060623084086, 'UPHENO:0020998', 'abnormal cornea morphology'),
(464140, 'HP:0001140', 'Limbal dermoid', 'XPO:0101315', 'abnormal hyaloid vascular plexus', 0.4305555555555556, 6.887869297006056, 1.7220947685207388, 'HP:0012372', 'Abnormal eye morphology'),
(464141, 'HP:0004471', 'Aplasia cutis congenita over the scalp vertex', 'XPO:0103147', 'abnormal neuromast mantle cell morphology', 0.40425531914893614, 7.420886955069779, 1.732031473267709, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(464142, 'HP:0004471', 'Aplasia cutis congenita over the scalp vertex', 'XPO:0102910', 'abnormal pigment cell morphology', 0.40425531914893614, 7.420886955069779, 1.732031473267709, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(464143, 'HP:0004471', 'Aplasia cutis congenita over the scalp vertex', 'XPO:0102840', 'abnormal stratum spongiosum morphology', 0.40425531914893614, 7.420886955069779, 1.732031473267709, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(464144, 'HP:0004471', 'Aplasia cutis congenita over the scalp vertex', 'XPO:0102727', 'abnormal skin seromucous gland morphology', 0.41304347826086957, 7.420886955069779, 1.7507566820385791, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(464145, 'HP:0004471', 'Aplasia cutis congenita over the scalp vertex', 'XPO:0102561', 'abnormal dermis morphology', 0.4222222222222222, 7.420886955069779, 1.7701026470319348, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(464146, 'HP:0004471', 'Aplasia cutis congenita over the scalp vertex', 'XPO:0102626', 'abnormal granular gland morphology', 0.41304347826086957, 7.420886955069779, 1.7507566820385791, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(464147, 'HP:0004471', 'Aplasia cutis congenita over the scalp vertex', 'XPO:0102176', 'abnormal neuromast support cell morphology', 0.40425531914893614, 7.420886955069779, 1.732031473267709, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(464148, 'HP:0004471', 'Aplasia cutis congenita over the scalp vertex', 'XPO:0100983', 'abnormal skin gland', 0.40540540540540543, 6.8660902472206855, 1.6683974647021622, 'HP:0000951', 'Abnormality of the skin'),
(464149, 'HP:0004471', 'Aplasia cutis congenita over the scalp vertex', 'XPO:0102139', 'abnormal skin morphology', 0.4318181818181818, 7.420886955069779, 1.7901044417621268, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(464150, 'HP:0004471', 'Aplasia cutis congenita over the scalp vertex', 'XPO:0102615', 'abnormal skin gland morphology', 0.4318181818181818, 7.420886955069779, 1.7901044417621268, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(464151, 'HP:0004471', 'Aplasia cutis congenita over the scalp vertex', 'XPO:0102886', 'abnormal stratum compactum morphology', 0.40425531914893614, 7.420886955069779, 1.732031473267709, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(464152, 'HP:0004471', 'Aplasia cutis congenita over the scalp vertex', 'XPO:0100507', 'abnormal skin', 0.4166666666666667, 6.8660902472206855, 1.6914109306558096, 'HP:0000951', 'Abnormality of the skin'),
(464153, 'HP:0004471', 'Aplasia cutis congenita over the scalp vertex', 'XPO:0102945', 'abnormal Eberth-Kastschenko layer morphology', 0.40425531914893614, 7.420886955069779, 1.732031473267709, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(464154, 'HP:0100661', 'Trigeminal neuralgia', 'XPO:0101421', 'abnormal oculomotor nerve', 0.45614035087719296, 8.429051634704384, 1.9608239518671824, 'HP:0045010', 'Abnormal peripheral nerve morphology by anatomical site'),
(464155, 'HP:0100661', 'Trigeminal neuralgia', 'XPO:0100110', 'abnormal trigeminal nerve', 0.45614035087719296, 8.429051634704384, 1.9608239518671824, 'HP:0045010', 'Abnormal peripheral nerve morphology by anatomical site'),
(464156, 'HP:0100661', 'Trigeminal neuralgia', 'XPO:0131679', 'abnormal frontal nerve', 0.4482758620689655, 8.429051634704384, 1.9438468015692314, 'HP:0045010', 'Abnormal peripheral nerve morphology by anatomical site'),
(464157, 'HP:0100661', 'Trigeminal neuralgia', 'XPO:0101596', 'abnormal accessory nerve', 0.4126984126984127, 8.429051634704384, 1.8651156077293065, 'HP:0045010', 'Abnormal peripheral nerve morphology by anatomical site'),
(464158, 'HP:0100661', 'Trigeminal neuralgia', 'XPO:0101030', 'abnormal spinal nerve', 0.4230769230769231, 8.429051634704384, 1.8884218887916013, 'HP:0045010', 'Abnormal peripheral nerve morphology by anatomical site'),
(464159, 'HP:0100661', 'Trigeminal neuralgia', 'XPO:0101207', 'abnormal glossopharyngeal nerve', 0.4406779661016949, 8.429051634704384, 1.9273031236802618, 'HP:0045010', 'Abnormal peripheral nerve morphology by anatomical site'),
(464160, 'HP:0100661', 'Trigeminal neuralgia', 'XPO:0131688', 'abnormal mandibular nerve', 0.4482758620689655, 8.429051634704384, 1.9438468015692314, 'HP:0045010', 'Abnormal peripheral nerve morphology by anatomical site'),
(464161, 'HP:0100661', 'Trigeminal neuralgia', 'XPO:0101204', 'abnormal peripheral nerve', 0.44, 8.429051634704384, 1.925820012168824, 'HP:0045010', 'Abnormal peripheral nerve morphology by anatomical site'),
(464162, 'HP:0100661', 'Trigeminal neuralgia', 'XPO:0100849', 'abnormal abducens nerve', 0.4126984126984127, 8.429051634704384, 1.8651156077293065, 'HP:0045010', 'Abnormal peripheral nerve morphology by anatomical site'),
(464163, 'HP:0100661', 'Trigeminal neuralgia', 'XPO:0101335', 'abnormal vagus nerve', 0.4406779661016949, 8.429051634704384, 1.9273031236802618, 'HP:0045010', 'Abnormal peripheral nerve morphology by anatomical site'),
(464164, 'HP:0100661', 'Trigeminal neuralgia', 'XPO:0131670', 'abnormal maxillary nerve', 0.4482758620689655, 8.429051634704384, 1.9438468015692314, 'HP:0045010', 'Abnormal peripheral nerve morphology by anatomical site'),
(464165, 'HP:0100661', 'Trigeminal neuralgia', 'XPO:0101118', 'abnormal trochlear nerve', 0.45614035087719296, 8.429051634704384, 1.9608239518671824, 'HP:0045010', 'Abnormal peripheral nerve morphology by anatomical site'),
(464166, 'HP:0100661', 'Trigeminal neuralgia', 'XPO:0101541', 'abnormal olfactory nerve', 0.4406779661016949, 8.429051634704384, 1.9273031236802618, 'HP:0045010', 'Abnormal peripheral nerve morphology by anatomical site'),
(464167, 'HP:0100661', 'Trigeminal neuralgia', 'XPO:0127916', 'abnormally localised facial nerve', 0.4177215189873418, 12.30515924801628, 2.267185438481488, 'UPHENO:0078730', 'abnormality of cranial nerve physiology'),
(464168, 'HP:0100661', 'Trigeminal neuralgia', 'XPO:0100111', 'abnormal cranial nerve', 0.4642857142857143, 8.429051634704384, 1.978253840883392, 'HP:0045010', 'Abnormal peripheral nerve morphology by anatomical site'),
(464169, 'HP:0100661', 'Trigeminal neuralgia', 'XPO:0100635', 'abnormal sympathetic chain', 0.4074074074074074, 8.429051634704384, 1.853121170727398, 'HP:0045010', 'Abnormal peripheral nerve morphology by anatomical site'),
(464170, 'HP:0100661', 'Trigeminal neuralgia', 'XPO:0100167', 'abnormal nerve', 0.44, 8.429051634704384, 1.925820012168824, 'HP:0045010', 'Abnormal peripheral nerve morphology by anatomical site'),
(464171, 'HP:0100661', 'Trigeminal neuralgia', 'XPO:0101855', 'abnormal facial nerve morphology', 0.4024390243902439, 12.30515924801628, 2.225326107054483, 'UPHENO:0078730', 'abnormality of cranial nerve physiology'),
(464172, 'HP:0100661', 'Trigeminal neuralgia', 'XPO:0101746', 'abnormal peripheral nervous system morphology', 0.40384615384615385, 7.318748312764234, 1.7191999177169197, 'HP:0000759', 'Abnormal peripheral nervous system morphology'),
(464173, 'HP:0100661', 'Trigeminal neuralgia', 'XPO:0131536', 'abnormally localised cephalic nerve', 0.4090909090909091, 8.429051634704384, 1.8569459862945477, 'HP:0045010', 'Abnormal peripheral nerve morphology by anatomical site'),
(464174, 'HP:0100661', 'Trigeminal neuralgia', 'XPO:0131652', 'abnormal cephalic nerve', 0.4727272727272727, 8.429051634704384, 1.9961569554900145, 'HP:0045010', 'Abnormal peripheral nerve morphology by anatomical site'),
(464175, 'HP:0100661', 'Trigeminal neuralgia', 'XPO:0131671', 'abnormal nasociliary nerve', 0.4482758620689655, 8.429051634704384, 1.9438468015692314, 'HP:0045010', 'Abnormal peripheral nerve morphology by anatomical site'),
(464176, 'HP:0100661', 'Trigeminal neuralgia', 'XPO:0100223', 'abnormal facial nerve', 0.5076923076923077, 12.30515924801628, 2.4994468778405206, 'UPHENO:0078730', 'abnormality of cranial nerve physiology'),
(464177, 'HP:0034924', 'Abnormal dermis morphology', 'XPO:0101141', 'abnormal Keller explant', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(464178, 'HP:0034924', 'Abnormal dermis morphology', 'XPO:0100004', 'abnormal cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(464179, 'HP:0034924', 'Abnormal dermis morphology', 'XPO:0101095', 'abnormal skin seromucous gland', 0.4838709677419355, 6.8660902472206855, 1.8227182263109507, 'HP:0000951', 'Abnormality of the skin'),
(464180, 'HP:0034924', 'Abnormal dermis morphology', 'XPO:0101004', 'abnormal acid secreting cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(464181, 'HP:0034924', 'Abnormal dermis morphology', 'XPO:0100258', 'abnormal organ part', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(464182, 'HP:0034924', 'Abnormal dermis morphology', 'XPO:0100994', 'abnormal granular gland', 0.4838709677419355, 6.8660902472206855, 1.8227182263109507, 'HP:0000951', 'Abnormality of the skin'),
(464183, 'HP:0034924', 'Abnormal dermis morphology', 'XPO:0100791', 'abnormal multiciliated cell precursor', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(464184, 'HP:0034924', 'Abnormal dermis morphology', 'XPO:0101237', 'abnormal mucus secreting cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(464185, 'HP:0034924', 'Abnormal dermis morphology', 'XPO:0131666', 'abnormal adherens junction', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(464186, 'HP:0034924', 'Abnormal dermis morphology', 'XPO:0100308', 'abnormal early embryonic cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(464187, 'HP:0034924', 'Abnormal dermis morphology', 'XPO:0100026', 'abnormal germ cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(464188, 'HP:0034924', 'Abnormal dermis morphology', 'XPO:0100691', 'abnormal keratin accumulating cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(464189, 'HP:0034924', 'Abnormal dermis morphology', 'XPO:0100704', 'abnormal Merkel cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(464190, 'HP:0034924', 'Abnormal dermis morphology', 'XPO:0103019', 'abnormal melanophore morphology', 0.4186046511627907, 7.420886955069779, 1.7625032752155354, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(464191, 'HP:0034924', 'Abnormal dermis morphology', 'XPO:0100544', 'abnormal neuromast support cell', 0.45454545454545453, 6.8660902472206855, 1.7666211003984522, 'HP:0000951', 'Abnormality of the skin'),
(464192, 'HP:0034924', 'Abnormal dermis morphology', 'XPO:0100108', 'abnormal cell part', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(464193, 'HP:0034924', 'Abnormal dermis morphology', 'XPO:0100172', 'abnormal stem cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(464194, 'HP:0034924', 'Abnormal dermis morphology', 'XPO:0101547', 'abnormal lampbrush chromosome', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(464195, 'HP:0034924', 'Abnormal dermis morphology', 'XPO:0100225', 'abnormal endocrine system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(464196, 'HP:0034924', 'Abnormal dermis morphology', 'XPO:0100724', 'abnormal kinetochore', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(464197, 'HP:0034924', 'Abnormal dermis morphology', 'XPO:0101435', 'abnormal paracrine cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(464198, 'HP:0034924', 'Abnormal dermis morphology', 'XPO:0100533', 'abnormal melanoblast', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(464199, 'HP:0034924', 'Abnormal dermis morphology', 'XPO:0101529', 'abnormal skin mucous gland', 0.45454545454545453, 6.8660902472206855, 1.7666211003984522, 'HP:0000951', 'Abnormality of the skin'),
(464200, 'HP:0034924', 'Abnormal dermis morphology', 'XPO:0103147', 'abnormal neuromast mantle cell morphology', 0.43902439024390244, 7.420886955069779, 1.8049793268950312, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(464201, 'HP:0034924', 'Abnormal dermis morphology', 'XPO:0101132', 'abnormal apoptotic cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(464202, 'HP:0034924', 'Abnormal dermis morphology', 'XPO:0100721', 'abnormal centromere', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(464203, 'HP:0034924', 'Abnormal dermis morphology', 'XPO:0100437', 'abnormal proepicardium', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(464204, 'HP:0034924', 'Abnormal dermis morphology', 'XPO:0100626', 'abnormal primordial germ cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(464205, 'HP:0034924', 'Abnormal dermis morphology', 'XPO:0100515', 'abnormal somatic stem cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(464206, 'HP:0034924', 'Abnormal dermis morphology', 'XPO:0100674', 'abnormal secondary oogonium', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(464207, 'HP:0034924', 'Abnormal dermis morphology', 'XPO:0101448', 'abnormal myelin accumulating cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(464208, 'HP:0034924', 'Abnormal dermis morphology', 'XPO:0101326', 'abnormal cementoblast', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(464209, 'HP:0034924', 'Abnormal dermis morphology', 'XPO:0102945', 'abnormal Eberth-Kastschenko layer morphology', 0.43902439024390244, 7.420886955069779, 1.8049793268950312, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(464210, 'HP:0034924', 'Abnormal dermis morphology', 'XPO:0100715', 'abnormal ciliated cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(464211, 'HP:0034924', 'Abnormal dermis morphology', 'XPO:0102139', 'abnormal skin morphology', 0.47368421052631576, 7.420886955069779, 1.8748751901706053, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(464212, 'HP:0034924', 'Abnormal dermis morphology', 'XPO:0131667', 'abnormal actin cytoskeleton', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(464213, 'HP:0034924', 'Abnormal dermis morphology', 'XPO:0103398', 'abnormally increased number of dense core granule in the goblet cell', 0.40540540540540543, 6.8660902472206855, 1.6683974647021622, 'HP:0000951', 'Abnormality of the skin'),
(464214, 'HP:0034924', 'Abnormal dermis morphology', 'XPO:0100344', 'abnormal portion of organism substance', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(464215, 'HP:0034924', 'Abnormal dermis morphology', 'XPO:0100507', 'abnormal skin', 0.5172413793103449, 6.8660902472206855, 1.8845227485869556, 'HP:0000951', 'Abnormality of the skin'),
(464216, 'HP:0034924', 'Abnormal dermis morphology', 'XPO:0100899', 'abnormal secondary spermatogonium', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(464217, 'HP:0034924', 'Abnormal dermis morphology', 'XPO:0107312', 'abnormal filopodium', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(464218, 'HP:0034924', 'Abnormal dermis morphology', 'XPO:0100289', 'abnormal chondroblast', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(464219, 'HP:0034924', 'Abnormal dermis morphology', 'XPO:0100501', 'abnormal urogenital system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(464220, 'HP:0034924', 'Abnormal dermis morphology', 'XPO:0101240', 'abnormal ciliated non-epidermal cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(464221, 'HP:0034924', 'Abnormal dermis morphology', 'XPO:0100285', 'abnormal progenitor cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(464222, 'HP:0034924', 'Abnormal dermis morphology', 'XPO:0100232', 'abnormal lymphatic system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(464223, 'HP:0034924', 'Abnormal dermis morphology', 'XPO:0101513', 'abnormal basal body', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(464224, 'HP:0034924', 'Abnormal dermis morphology', 'XPO:0101297', 'abnormal barrier cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(464225, 'HP:0034924', 'Abnormal dermis morphology', 'XPO:0102176', 'abnormal neuromast support cell morphology', 0.43902439024390244, 7.420886955069779, 1.8049793268950312, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(464226, 'HP:0034924', 'Abnormal dermis morphology', 'XPO:0101208', 'abnormal stratum spongiosum', 0.45454545454545453, 6.8660902472206855, 1.7666211003984522, 'HP:0000951', 'Abnormality of the skin'),
(464227, 'HP:0034924', 'Abnormal dermis morphology', 'XPO:0100976', 'abnormal multiciliated cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(464228, 'HP:0034924', 'Abnormal dermis morphology', 'XPO:0102561', 'abnormal dermis morphology', 0.46153846153846156, 7.420886955069779, 1.8506822386605823, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(464229, 'HP:0034924', 'Abnormal dermis morphology', 'XPO:0140154', 'abnormally necrotic skin', 0.4090909090909091, 7.420886955069779, 1.7423597190908553, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(464230, 'HP:0034924', 'Abnormal dermis morphology', 'XPO:0100888', 'abnormal microtubule', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(464231, 'HP:0034924', 'Abnormal dermis morphology', 'XPO:0101313', 'abnormal Eberth-Kastschenko layer', 0.45454545454545453, 6.8660902472206855, 1.7666211003984522, 'HP:0000951', 'Abnormality of the skin'),
(464232, 'HP:0034924', 'Abnormal dermis morphology', 'XPO:0101254', 'abnormal stratum compactum', 0.45454545454545453, 6.8660902472206855, 1.7666211003984522, 'HP:0000951', 'Abnormality of the skin'),
(464233, 'HP:0034924', 'Abnormal dermis morphology', 'XPO:0140540', 'abnormally necrotic dermis', 0.4090909090909091, 7.420886955069779, 1.7423597190908553, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(464234, 'HP:0034924', 'Abnormal dermis morphology', 'XPO:0103161', 'abnormal skin mucous gland morphology', 0.4090909090909091, 7.420886955069779, 1.7423597190908553, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(464235, 'HP:0034924', 'Abnormal dermis morphology', 'XPO:0100549', 'abnormal mitotic cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(464236, 'HP:0034924', 'Abnormal dermis morphology', 'XPO:0140591', 'abnormally necrotic skin gland', 0.4090909090909091, 7.420886955069779, 1.7423597190908553, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(464237, 'HP:0034924', 'Abnormal dermis morphology', 'XPO:0100907', 'abnormal cytoplasm', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(464238, 'HP:0034924', 'Abnormal dermis morphology', 'XPO:0100429', 'abnormal spermatid', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(464239, 'HP:0034924', 'Abnormal dermis morphology', 'XPO:0103223', 'abnormal xanthophore morphology', 0.4186046511627907, 7.420886955069779, 1.7625032752155354, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(464240, 'HP:0034924', 'Abnormal dermis morphology', 'XPO:0101591', 'abnormal xanthophore', 0.4411764705882353, 6.8660902472206855, 1.740447489012273, 'HP:0000951', 'Abnormality of the skin'),
(464241, 'HP:0034924', 'Abnormal dermis morphology', 'XPO:0101071', 'abnormal endoplasmic reticulum', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(464242, 'HP:0034924', 'Abnormal dermis morphology', 'XPO:0107284', 'abnormal migrating myoblast', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(464243, 'HP:0034924', 'Abnormal dermis morphology', 'XPO:0102840', 'abnormal stratum spongiosum morphology', 0.43902439024390244, 7.420886955069779, 1.8049793268950312, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(464244, 'HP:0034924', 'Abnormal dermis morphology', 'XPO:0102727', 'abnormal skin seromucous gland morphology', 0.45, 7.420886955069779, 1.8274022900777487, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(464245, 'HP:0034924', 'Abnormal dermis morphology', 'XPO:0100802', 'abnormal exocrine cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(464246, 'HP:0034924', 'Abnormal dermis morphology', 'XPO:0100983', 'abnormal skin gland', 0.5, 6.8660902472206855, 1.8528478414619864, 'HP:0000951', 'Abnormality of the skin'),
(464247, 'HP:0034924', 'Abnormal dermis morphology', 'XPO:0102615', 'abnormal skin gland morphology', 0.47368421052631576, 7.420886955069779, 1.8748751901706053, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(464248, 'HP:0034924', 'Abnormal dermis morphology', 'XPO:0101061', 'abnormal plasma membrane', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(464249, 'HP:0034924', 'Abnormal dermis morphology', 'XPO:0100956', 'abnormal centrosome', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(464250, 'HP:0034924', 'Abnormal dermis morphology', 'XPO:0101387', 'abnormal melanophore', 0.4411764705882353, 6.8660902472206855, 1.740447489012273, 'HP:0000951', 'Abnormality of the skin'),
(464251, 'HP:0034924', 'Abnormal dermis morphology', 'XPO:0107258', 'abnormal anatomical axis', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(464252, 'HP:0034924', 'Abnormal dermis morphology', 'XPO:0102626', 'abnormal granular gland morphology', 0.45, 7.420886955069779, 1.8274022900777487, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(464253, 'HP:0034924', 'Abnormal dermis morphology', 'XPO:0101228', 'abnormal mesenchymal stem cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(464254, 'HP:0034924', 'Abnormal dermis morphology', 'XPO:0101569', 'abnormal activin-induced ectoderm', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(464255, 'HP:0034924', 'Abnormal dermis morphology', 'XPO:0100653', 'abnormal myoblast', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(464256, 'HP:0034924', 'Abnormal dermis morphology', 'XPO:0101515', 'abnormal neuromast mantle cell', 0.45454545454545453, 6.8660902472206855, 1.7666211003984522, 'HP:0000951', 'Abnormality of the skin'),
(464257, 'HP:0034924', 'Abnormal dermis morphology', 'XPO:0100006', 'abnormal anatomical structure', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(464258, 'HP:0034924', 'Abnormal dermis morphology', 'XPO:0100481', 'abnormal anatomical line', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(464259, 'HP:0034924', 'Abnormal dermis morphology', 'XPO:0101535', 'abnormal absorptive cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(464260, 'HP:0034924', 'Abnormal dermis morphology', 'XPO:0101264', 'abnormal mitotic spindle', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(464261, 'HP:0034924', 'Abnormal dermis morphology', 'XPO:0100372', 'abnormal hematological system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(464262, 'HP:0034924', 'Abnormal dermis morphology', 'XPO:0100477', 'abnormal pericyte', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(464263, 'HP:0034924', 'Abnormal dermis morphology', 'XPO:0101278', 'abnormal pigment cell', 0.45454545454545453, 6.8660902472206855, 1.7666211003984522, 'HP:0000951', 'Abnormality of the skin'),
(464264, 'HP:0034924', 'Abnormal dermis morphology', 'XPO:0101322', 'abnormal iridophore', 0.4411764705882353, 6.8660902472206855, 1.740447489012273, 'HP:0000951', 'Abnormality of the skin'),
(464265, 'HP:0034924', 'Abnormal dermis morphology', 'XPO:0100546', 'abnormal whole organism', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(464266, 'HP:0034924', 'Abnormal dermis morphology', 'XPO:0100894', 'abnormal nucleus', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(464267, 'HP:0034924', 'Abnormal dermis morphology', 'XPO:0101110', 'abnormal cell-free extract', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(464268, 'HP:0034924', 'Abnormal dermis morphology', 'XPO:0101467', 'abnormal alkali secreting cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(464269, 'HP:0034924', 'Abnormal dermis morphology', 'XPO:0100317', 'abnormal respiratory system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(464270, 'HP:0034924', 'Abnormal dermis morphology', 'XPO:0101014', 'abnormal goblet cell', 0.4166666666666667, 6.8660902472206855, 1.6914109306558096, 'HP:0000951', 'Abnormality of the skin'),
(464271, 'HP:0034924', 'Abnormal dermis morphology', 'XPO:0100008', 'abnormal epidermis', 0.40540540540540543, 6.8660902472206855, 1.6683974647021622, 'HP:0000951', 'Abnormality of the skin'),
(464272, 'HP:0034924', 'Abnormal dermis morphology', 'XPO:0102886', 'abnormal stratum compactum morphology', 0.43902439024390244, 7.420886955069779, 1.8049793268950312, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(464273, 'HP:0034924', 'Abnormal dermis morphology', 'XPO:0100969', 'abnormal disaggregated/reaggregated ectoderm treated with activin', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(464274, 'HP:0034924', 'Abnormal dermis morphology', 'XPO:0142057', 'abnormal desmosome', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(464275, 'HP:0034924', 'Abnormal dermis morphology', 'XPO:0100025', 'abnormal oocyte', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(464276, 'HP:0034924', 'Abnormal dermis morphology', 'XPO:0102910', 'abnormal pigment cell morphology', 0.43902439024390244, 7.420886955069779, 1.8049793268950312, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(464277, 'HP:0034924', 'Abnormal dermis morphology', 'XPO:0100902', 'abnormal spermatocyte', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(464278, 'HP:0034924', 'Abnormal dermis morphology', 'XPO:0100852', 'abnormal interdigital region', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(464279, 'HP:0034924', 'Abnormal dermis morphology', 'XPO:0100638', 'abnormal polar body', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(464280, 'HP:0034924', 'Abnormal dermis morphology', 'XPO:0100754', 'abnormal electrically active cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(464281, 'HP:0034924', 'Abnormal dermis morphology', 'XPO:0100081', 'abnormal anatomical entity in vitro', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(464282, 'HP:0034924', 'Abnormal dermis morphology', 'XPO:0101333', 'abnormal barrier epithelial cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(464283, 'HP:0034924', 'Abnormal dermis morphology', 'XPO:0101373', 'abnormal oxygen accumulating cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(464284, 'HP:0034924', 'Abnormal dermis morphology', 'XPO:0100032', 'abnormal nervous system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(464285, 'HP:0034924', 'Abnormal dermis morphology', 'XPO:0101241', 'abnormal nucleate erythrocyte', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(464286, 'HP:0034924', 'Abnormal dermis morphology', 'XPO:0100929', 'abnormal dermis', 0.4838709677419355, 6.8660902472206855, 1.8227182263109507, 'HP:0000951', 'Abnormality of the skin'),
(464287, 'HP:0034924', 'Abnormal dermis morphology', 'XPO:0102954', 'abnormal iridophore morphology', 0.4186046511627907, 7.420886955069779, 1.7625032752155354, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(464288, 'HP:0034924', 'Abnormal dermis morphology', 'XPO:0100337', 'abnormal zygote', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(464289, 'HP:0034924', 'Abnormal dermis morphology', 'XPO:0100581', 'abnormal immune system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(464290, 'HP:0001181', 'Adducted thumb', 'XPO:0129161', 'decreased size of the forelimb digit 5', 0.4842105263157895, 7.492661022682715, 1.904737603266917, 'HP:0001167', 'Abnormal finger morphology'),
(464291, 'HP:0001181', 'Adducted thumb', 'XPO:0103280', 'absent forelimb digit 3', 0.4423076923076923, 7.492661022682715, 1.820456427983539, 'HP:0001167', 'Abnormal finger morphology'),
(464292, 'HP:0001181', 'Adducted thumb', 'XPO:0103755', 'increased size of the forelimb digit', 0.5054945054945055, 7.492661022682715, 1.9461497831613463, 'HP:0001167', 'Abnormal finger morphology'),
(464293, 'HP:0001181', 'Adducted thumb', 'XPO:0103279', 'absent forelimb digit 2', 0.4423076923076923, 7.492661022682715, 1.820456427983539, 'HP:0001167', 'Abnormal finger morphology'),
(464294, 'HP:0001181', 'Adducted thumb', 'XPO:0103632', 'abnormally increased number of digit', 0.4027777777777778, 6.393467666143939, 1.6047263626124957, 'UPHENO:0002905', 'abnormal digit'),
(464295, 'HP:0001181', 'Adducted thumb', 'XPO:0102214', 'abnormal forelimb digit morphology', 0.5679012345679012, 7.492661022682715, 2.062787299985218, 'HP:0001167', 'Abnormal finger morphology'),
(464296, 'HP:0001181', 'Adducted thumb', 'XPO:0102880', 'abnormal digit-joint region morphology', 0.5074626865671642, 6.466375519622663, 1.8114757225919036, 'UPHENO:0086700', 'abnormal digit morphology'),
(464297, 'HP:0001181', 'Adducted thumb', 'XPO:0103622', 'abnormal number of forelimb digit 5', 0.4230769230769231, 7.059765001318215, 1.7282429384793851, 'UPHENO:0002708', 'abnormal manus'),
(464298, 'HP:0001181', 'Adducted thumb', 'XPO:0103619', 'abnormal number of forelimb digit 2', 0.4230769230769231, 7.059765001318215, 1.7282429384793851, 'UPHENO:0002708', 'abnormal manus'),
(464299, 'HP:0001181', 'Adducted thumb', 'XPO:0103620', 'abnormal number of forelimb digit 3', 0.4230769230769231, 7.059765001318215, 1.7282429384793851, 'UPHENO:0002708', 'abnormal manus'),
(464300, 'HP:0001181', 'Adducted thumb', 'XPO:0103466', 'bifurcated forelimb digit 3', 0.46, 7.492661022682715, 1.8565085699866966, 'HP:0001167', 'Abnormal finger morphology'),
(464301, 'HP:0001181', 'Adducted thumb', 'XPO:0103281', 'absent forelimb digit 4', 0.4423076923076923, 7.492661022682715, 1.820456427983539, 'HP:0001167', 'Abnormal finger morphology'),
(464302, 'HP:0001181', 'Adducted thumb', 'XPO:0103621', 'abnormal number of forelimb digit 4', 0.4230769230769231, 7.059765001318215, 1.7282429384793851, 'UPHENO:0002708', 'abnormal manus'),
(464303, 'HP:0001181', 'Adducted thumb', 'XPO:0140716', 'abnormally necrotic forelimb digit 4', 0.5, 7.492661022682715, 1.935543983313569, 'HP:0001167', 'Abnormal finger morphology'),
(464304, 'HP:0001181', 'Adducted thumb', 'XPO:0141108', 'abnormally necrotic forelimb digit 2', 0.5, 7.492661022682715, 1.935543983313569, 'HP:0001167', 'Abnormal finger morphology'),
(464305, 'HP:0001181', 'Adducted thumb', 'XPO:0102746', 'abnormal forelimb digit 2 morphology', 0.5542168674698795, 7.492661022682715, 2.0377828934910798, 'HP:0001167', 'Abnormal finger morphology'),
(464306, 'HP:0001181', 'Adducted thumb', 'XPO:0140219', 'abnormally necrotic forelimb digit', 0.5168539325842697, 7.492661022682715, 1.9678951483995373, 'HP:0001167', 'Abnormal finger morphology'),
(464307, 'HP:0001181', 'Adducted thumb', 'XPO:0130637', 'increased size of the forelimb digit 5', 0.48936170212765956, 7.492661022682715, 1.914842382945809, 'HP:0001167', 'Abnormal finger morphology'),
(464308, 'HP:0001181', 'Adducted thumb', 'XPO:0103467', 'bifurcated forelimb digit 4', 0.46, 7.492661022682715, 1.8565085699866966, 'HP:0001167', 'Abnormal finger morphology'),
(464309, 'HP:0001181', 'Adducted thumb', 'XPO:0141143', 'abnormally necrotic forelimb digit 3', 0.5, 7.492661022682715, 1.935543983313569, 'HP:0001167', 'Abnormal finger morphology'),
(464310, 'HP:0001181', 'Adducted thumb', 'XPO:0100178', 'abnormal digit', 0.45901639344262296, 6.393467666143939, 1.7130984997090548, 'HP:0011297', 'Abnormal digit morphology'),
(464311, 'HP:0001181', 'Adducted thumb', 'XPO:0133378', 'fused forelimb digits part of regenerating forelimb', 0.4742268041237113, 7.492661022682715, 1.8849988570736913, 'HP:0001167', 'Abnormal finger morphology'),
(464312, 'HP:0001181', 'Adducted thumb', 'XPO:0129148', 'decreased size of the forelimb digit 4', 0.4842105263157895, 7.492661022682715, 1.904737603266917, 'HP:0001167', 'Abnormal finger morphology'),
(464313, 'HP:0001181', 'Adducted thumb', 'XPO:0128213', 'decreased size of the digit', 0.4473684210526316, 6.466375519622663, 1.7008386772845274, 'UPHENO:0086700', 'abnormal digit morphology'),
(464314, 'HP:0001181', 'Adducted thumb', 'XPO:0103609', 'abnormally increased number of forelimb digit in the regenerating forelimb', 0.41818181818181815, 7.492661022682715, 1.7701114680961476, 'HP:0001167', 'Abnormal finger morphology'),
(464315, 'HP:0001181', 'Adducted thumb', 'XPO:0140898', 'abnormally necrotic forelimb digit 5', 0.5, 7.492661022682715, 1.935543983313569, 'HP:0001167', 'Abnormal finger morphology'),
(464316, 'HP:0001181', 'Adducted thumb', 'XPO:0129977', 'increased size of the digit-joint region', 0.4657534246575342, 6.466375519622663, 1.7354355486119033, 'UPHENO:0086700', 'abnormal digit morphology'),
(464317, 'HP:0001181', 'Adducted thumb', 'XPO:0129188', 'decreased size of the forelimb digit 2', 0.4842105263157895, 7.492661022682715, 1.904737603266917, 'HP:0001167', 'Abnormal finger morphology'),
(464318, 'HP:0001181', 'Adducted thumb', 'XPO:0101810', 'abnormal digit morphology', 0.5074626865671642, 6.466375519622663, 1.8114757225919036, 'UPHENO:0086700', 'abnormal digit morphology'),
(464319, 'HP:0001181', 'Adducted thumb', 'XPO:0125257', 'absent forelimb digit', 0.45544554455445546, 7.492661022682715, 1.8472950710803275, 'HP:0001167', 'Abnormal finger morphology'),
(464320, 'HP:0001181', 'Adducted thumb', 'XPO:0128497', 'decreased size of the digit-joint region', 0.4657534246575342, 6.466375519622663, 1.7354355486119033, 'UPHENO:0086700', 'abnormal digit morphology'),
(464321, 'HP:0001181', 'Adducted thumb', 'XPO:0130624', 'increased size of the forelimb digit 4', 0.48936170212765956, 7.492661022682715, 1.914842382945809, 'HP:0001167', 'Abnormal finger morphology'),
(464322, 'HP:0001181', 'Adducted thumb', 'XPO:0103282', 'absent forelimb digit 5', 0.4423076923076923, 7.492661022682715, 1.820456427983539, 'HP:0001167', 'Abnormal finger morphology'),
(464323, 'HP:0001181', 'Adducted thumb', 'XPO:0103611', 'abnormal number of forelimb digits', 0.4342105263157895, 7.059765001318215, 1.7508353083280486, 'UPHENO:0002708', 'abnormal manus'),
(464324, 'HP:0001181', 'Adducted thumb', 'XPO:0103468', 'bifurcated forelimb digit 5', 0.46, 7.492661022682715, 1.8565085699866966, 'HP:0001167', 'Abnormal finger morphology'),
(464325, 'HP:0001181', 'Adducted thumb', 'XPO:0101248', 'abnormal digit-joint region', 0.4375, 6.393467666143939, 1.6724658752686028, 'UPHENO:0002905', 'abnormal digit'),
(464326, 'HP:0001181', 'Adducted thumb', 'XPO:0100966', 'abnormal forelimb digit 3', 0.43243243243243246, 7.059765001318215, 1.747246791933352, 'UPHENO:0002708', 'abnormal manus'),
(464327, 'HP:0001181', 'Adducted thumb', 'XPO:0128172', 'decreased size of the forelimb digit 3', 0.4842105263157895, 7.492661022682715, 1.904737603266917, 'HP:0001167', 'Abnormal finger morphology'),
(464328, 'HP:0001181', 'Adducted thumb', 'XPO:0129693', 'increased size of the digit', 0.4473684210526316, 6.466375519622663, 1.7008386772845274, 'UPHENO:0086700', 'abnormal digit morphology'),
(464329, 'HP:0001181', 'Adducted thumb', 'XPO:0103432', 'decreased size of the forelimb digit', 0.5, 7.492661022682715, 1.935543983313569, 'HP:0001167', 'Abnormal finger morphology'),
(464330, 'HP:0001181', 'Adducted thumb', 'XPO:0141569', 'abnormal digit-joint region morphology in the regenerating hindlimb', 0.4657534246575342, 6.466375519622663, 1.7354355486119033, 'UPHENO:0086700', 'abnormal digit morphology'),
(464331, 'HP:0001181', 'Adducted thumb', 'XPO:0103465', 'bifurcated forelimb digit 2', 0.46, 7.492661022682715, 1.8565085699866966, 'HP:0001167', 'Abnormal finger morphology'),
(464332, 'HP:0001181', 'Adducted thumb', 'XPO:0103634', 'abnormally increased number of forelimb digit', 0.4423076923076923, 7.492661022682715, 1.820456427983539, 'HP:0001167', 'Abnormal finger morphology'),
(464333, 'HP:0001181', 'Adducted thumb', 'XPO:0101114', 'abnormal forelimb digit 2', 0.43243243243243246, 7.059765001318215, 1.747246791933352, 'UPHENO:0002708', 'abnormal manus'),
(464334, 'HP:0001181', 'Adducted thumb', 'XPO:0101155', 'abnormal forelimb digit 5', 0.43243243243243246, 7.059765001318215, 1.747246791933352, 'UPHENO:0002708', 'abnormal manus'),
(464335, 'HP:0001181', 'Adducted thumb', 'XPO:0102529', 'abnormal forelimb digit 4 morphology', 0.5542168674698795, 7.492661022682715, 2.0377828934910798, 'HP:0001167', 'Abnormal finger morphology'),
(464336, 'HP:0001181', 'Adducted thumb', 'XPO:0141556', 'abnormal forelimb digit morphology in the regenerating forelimb', 0.5287356321839081, 7.492661022682715, 1.990386108916527, 'HP:0001167', 'Abnormal finger morphology'),
(464337, 'HP:0001181', 'Adducted thumb', 'XPO:0133358', 'fused forelimb digits', 0.5111111111111111, 7.492661022682715, 1.9569318589266915, 'HP:0001167', 'Abnormal finger morphology'),
(464338, 'HP:0001181', 'Adducted thumb', 'XPO:0103779', 'decreased size of the forelimb digit in the regenerating forelimb', 0.46464646464646464, 7.492661022682715, 1.8658613171894334, 'HP:0001167', 'Abnormal finger morphology'),
(464339, 'HP:0001181', 'Adducted thumb', 'XPO:0102787', 'abnormal forelimb digit 5 morphology', 0.5542168674698795, 7.492661022682715, 2.0377828934910798, 'HP:0001167', 'Abnormal finger morphology'),
(464340, 'HP:0001181', 'Adducted thumb', 'XPO:0129652', 'increased size of the forelimb digit 3', 0.48936170212765956, 7.492661022682715, 1.914842382945809, 'HP:0001167', 'Abnormal finger morphology'),
(464341, 'HP:0001181', 'Adducted thumb', 'XPO:0139962', 'abnormally necrotic digit', 0.4594594594594595, 6.466375519622663, 1.723669748213883, 'UPHENO:0086700', 'abnormal digit morphology'),
(464342, 'HP:0001181', 'Adducted thumb', 'XPO:0102598', 'abnormal forelimb digit 3 morphology', 0.5542168674698795, 7.492661022682715, 2.0377828934910798, 'HP:0001167', 'Abnormal finger morphology'),
(464343, 'HP:0001181', 'Adducted thumb', 'XPO:0141568', 'abnormal digit-joint region morphology in the regenerating forelimb', 0.4657534246575342, 6.466375519622663, 1.7354355486119033, 'UPHENO:0086700', 'abnormal digit morphology'),
(464344, 'HP:0001181', 'Adducted thumb', 'XPO:0100582', 'abnormal forelimb digit', 0.4383561643835616, 7.059765001318215, 1.7591735296516835, 'UPHENO:0002708', 'abnormal manus'),
(464345, 'HP:0001181', 'Adducted thumb', 'XPO:0126603', 'abnormally localised digit', 0.4027777777777778, 6.393467666143939, 1.6047263626124957, 'UPHENO:0002905', 'abnormal digit'),
(464346, 'HP:0001181', 'Adducted thumb', 'XPO:0100897', 'abnormal forelimb digit 4', 0.43243243243243246, 7.059765001318215, 1.747246791933352, 'UPHENO:0002708', 'abnormal manus'),
(464347, 'HP:0001181', 'Adducted thumb', 'XPO:0141208', 'abnormally necrotic digit-joint region', 0.4788732394366197, 6.466375519622663, 1.7597085532824348, 'UPHENO:0086700', 'abnormal digit morphology'),
(464348, 'HP:0001181', 'Adducted thumb', 'XPO:0127078', 'abnormally localised digit-joint region', 0.4084507042253521, 6.393467666143939, 1.6159877384059913, 'HP:0011297', 'Abnormal digit morphology'),
(464349, 'HP:0001181', 'Adducted thumb', 'XPO:0130664', 'increased size of the forelimb digit 2', 0.48936170212765956, 7.492661022682715, 1.914842382945809, 'HP:0001167', 'Abnormal finger morphology'),
(464350, 'HP:0005539', 'T cell chronic lymphocytic lymphoma/leukemia', 'XPO:0101450', 'abnormal myeloid cell', 0.40540540540540543, 5.574066539846944, 1.5032487170602729, 'UPHENO:0004459', 'abnormal hematopoietic system'),
(464351, 'HP:0005539', 'T cell chronic lymphocytic lymphoma/leukemia', 'XPO:0100449', 'abnormal lymphocyte', 0.40540540540540543, 5.64885357140806, 1.5132996306721471, 'HP:0002715', 'Abnormality of the immune system'),
(464352, 'HP:0005539', 'T cell chronic lymphocytic lymphoma/leukemia', 'XPO:0101107', 'abnormal erythroid cell', 0.40540540540540543, 5.574066539846944, 1.5032487170602729, 'UPHENO:0004459', 'abnormal hematopoietic system'),
(464353, 'HP:0005539', 'T cell chronic lymphocytic lymphoma/leukemia', 'XPO:0141497', 'abnormal lymphoblast', 0.40540540540540543, 5.64885357140806, 1.5132996306721471, 'HP:0002715', 'Abnormality of the immune system'),
(464354, 'HP:0005539', 'T cell chronic lymphocytic lymphoma/leukemia', 'XPO:0101587', 'abnormal hemangioblast', 0.40540540540540543, 5.574066539846944, 1.5032487170602729, 'HP:0001871', 'Abnormality of blood and blood-forming tissues'),
(464355, 'HP:0002779', 'Tracheomalacia', 'XPO:0128581', 'decreased size of the trachea', 0.42857142857142855, 12.7857850889227, 2.3408592826068957, 'UPHENO:0021304', 'abnormal trachea morphology'),
(464356, 'HP:0002779', 'Tracheomalacia', 'XPO:0101548', 'abnormal pulmonary vein', 0.4067796610169492, 7.241224942262181, 1.7162700916117157, 'HP:0012252', 'Abnormal respiratory system morphology'),
(464357, 'HP:0002779', 'Tracheomalacia', 'XPO:0115387', 'abnormal agenesis of trachea', 0.5084745762711864, 12.7857850889227, 2.5497542343105195, 'UPHENO:0021304', 'abnormal trachea morphology'),
(464358, 'HP:0002779', 'Tracheomalacia', 'XPO:0100586', 'abnormal thyroid primordium', 0.4444444444444444, 7.241224942262181, 1.793968281927239, 'HP:0012252', 'Abnormal respiratory system morphology'),
(464359, 'HP:0002779', 'Tracheomalacia', 'XPO:0101036', 'abnormal pharynx', 0.48, 7.241224942262181, 1.8643465268790154, 'HP:0012252', 'Abnormal respiratory system morphology'),
(464360, 'HP:0002779', 'Tracheomalacia', 'XPO:0127859', 'abnormally localised larynx', 0.42857142857142855, 7.241224942262181, 1.7616418813460253, 'HP:0012252', 'Abnormal respiratory system morphology'),
(464361, 'HP:0002779', 'Tracheomalacia', 'XPO:0141644', 'neoplastic larynx', 0.42105263157894735, 7.241224942262181, 1.746120504946495, 'HP:0012252', 'Abnormal respiratory system morphology'),
(464362, 'HP:0002779', 'Tracheomalacia', 'XPO:0130015', 'increased size of the respiratory system', 0.5, 7.241224942262181, 1.9027907060764961, 'HP:0012252', 'Abnormal respiratory system morphology'),
(464363, 'HP:0002779', 'Tracheomalacia', 'XPO:0100210', 'abnormal pulmonary artery', 0.4067796610169492, 7.241224942262181, 1.7162700916117157, 'HP:0012252', 'Abnormal respiratory system morphology'),
(464364, 'HP:0002779', 'Tracheomalacia', 'XPO:0126197', 'absent larynx', 0.42105263157894735, 7.241224942262181, 1.746120504946495, 'HP:0012252', 'Abnormal respiratory system morphology'),
(464365, 'HP:0002779', 'Tracheomalacia', 'XPO:0102436', 'abnormal larynx morphology', 0.4444444444444444, 7.241224942262181, 1.793968281927239, 'HP:0012252', 'Abnormal respiratory system morphology'),
(464366, 'HP:0002779', 'Tracheomalacia', 'XPO:0102668', 'abnormal pharynx morphology', 0.41379310344827586, 7.241224942262181, 1.7310022939400542, 'HP:0012252', 'Abnormal respiratory system morphology'),
(464367, 'HP:0002779', 'Tracheomalacia', 'XPO:0128535', 'decreased size of the respiratory system', 0.5, 7.241224942262181, 1.9027907060764961, 'HP:0012252', 'Abnormal respiratory system morphology'),
(464368, 'HP:0002779', 'Tracheomalacia', 'XPO:0130061', 'increased size of the trachea', 0.4225352112676056, 12.7857850889227, 2.32431590016722, 'UPHENO:0021304', 'abnormal trachea morphology'),
(464369, 'HP:0002779', 'Tracheomalacia', 'XPO:0101949', 'abnormal respiratory system morphology', 0.5853658536585366, 7.241224942262181, 2.058826320955896, 'HP:0012252', 'Abnormal respiratory system morphology'),
(464370, 'HP:0002779', 'Tracheomalacia', 'XPO:0102974', 'abnormal trachea morphology', 0.5263157894736842, 12.7857850889227, 2.594101110812223, 'UPHENO:0021304', 'abnormal trachea morphology'),
(464371, 'HP:0002779', 'Tracheomalacia', 'XPO:0102528', 'abnormal bronchus morphology', 0.4576271186440678, 10.802658907487096, 2.2234184647807513, 'HP:0005607', 'Abnormal tracheobronchial morphology'),
(464372, 'HP:0002779', 'Tracheomalacia', 'XPO:0125232', 'absent pharynx', 0.4067796610169492, 7.241224942262181, 1.7162700916117157, 'HP:0012252', 'Abnormal respiratory system morphology'),
(464373, 'HP:0002779', 'Tracheomalacia', 'XPO:0141660', 'neoplastic trachea', 0.5, 12.7857850889227, 2.5284170036727227, 'UPHENO:0021304', 'abnormal trachea morphology'),
(464374, 'HP:0002779', 'Tracheomalacia', 'XPO:0141634', 'neoplastic bronchus', 0.43548387096774194, 10.802658907487096, 2.1689591323435855, 'HP:0005607', 'Abnormal tracheobronchial morphology'),
(464375, 'HP:0002779', 'Tracheomalacia', 'XPO:0101329', 'abnormal pharyngeal epithelium', 0.47058823529411764, 7.241224942262181, 1.8459781328463531, 'HP:0012252', 'Abnormal respiratory system morphology'),
(464376, 'HP:0002779', 'Tracheomalacia', 'XPO:0100804', 'abnormal larynx', 0.5217391304347826, 7.241224942262181, 1.9437156182576012, 'HP:0012252', 'Abnormal respiratory system morphology'),
(464377, 'HP:0002779', 'Tracheomalacia', 'XPO:0126855', 'abnormally localised pharynx', 0.41379310344827586, 7.241224942262181, 1.7310022939400542, 'HP:0012252', 'Abnormal respiratory system morphology'),
(464378, 'HP:0002779', 'Tracheomalacia', 'XPO:0141305', 'abnormal tracheal epithelium morphology', 0.4375, 11.854497839006713, 2.2773543432161447, 'UPHENO:0087816', 'abnormal trachea morphology'),
(464379, 'HP:0002779', 'Tracheomalacia', 'XPO:0139850', 'abnormally necrotic respiratory system', 0.5217391304347826, 7.241224942262181, 1.9437156182576012, 'HP:0012252', 'Abnormal respiratory system morphology'),
(464380, 'HP:0002779', 'Tracheomalacia', 'XPO:0139900', 'abnormally necrotic trachea', 0.44776119402985076, 12.7857850889227, 2.3926927086496272, 'UPHENO:0021304', 'abnormal trachea morphology'),
(464381, 'HP:0002779', 'Tracheomalacia', 'XPO:0141614', 'metaplastic larynx', 0.4897959183673469, 7.241224942262181, 1.8832743880539138, 'HP:0012252', 'Abnormal respiratory system morphology'),
(464382, 'HP:0002779', 'Tracheomalacia', 'XPO:0100875', 'abnormal oropharynx', 0.4528301886792453, 7.241224942262181, 1.810813424092455, 'HP:0012252', 'Abnormal respiratory system morphology'),
(464383, 'HP:0031384', 'Reduced T cell CD40 expression', 'XPO:0100802', 'abnormal exocrine cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(464384, 'HP:0031384', 'Reduced T cell CD40 expression', 'XPO:0101132', 'abnormal apoptotic cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(464385, 'HP:0031384', 'Reduced T cell CD40 expression', 'XPO:0100715', 'abnormal ciliated cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(464386, 'HP:0031384', 'Reduced T cell CD40 expression', 'XPO:0100704', 'abnormal Merkel cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(464387, 'HP:0031384', 'Reduced T cell CD40 expression', 'XPO:0126730', 'abnormally localised immune system', 0.4117647058823529, 5.64885357140806, 1.525122463739656, 'HP:0002715', 'Abnormality of the immune system'),
(464388, 'HP:0031384', 'Reduced T cell CD40 expression', 'XPO:0101297', 'abnormal barrier cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(464389, 'HP:0031384', 'Reduced T cell CD40 expression', 'XPO:0101333', 'abnormal barrier epithelial cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(464390, 'HP:0031384', 'Reduced T cell CD40 expression', 'XPO:0101535', 'abnormal absorptive cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(464391, 'HP:0031384', 'Reduced T cell CD40 expression', 'XPO:0100172', 'abnormal stem cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(464392, 'HP:0031384', 'Reduced T cell CD40 expression', 'XPO:0101373', 'abnormal oxygen accumulating cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(464393, 'HP:0031384', 'Reduced T cell CD40 expression', 'XPO:0100344', 'abnormal portion of organism substance', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(464394, 'HP:0031384', 'Reduced T cell CD40 expression', 'XPO:0100691', 'abnormal keratin accumulating cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(464395, 'HP:0031384', 'Reduced T cell CD40 expression', 'XPO:0101004', 'abnormal acid secreting cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(464396, 'HP:0031384', 'Reduced T cell CD40 expression', 'XPO:0101467', 'abnormal alkali secreting cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(464397, 'HP:0031384', 'Reduced T cell CD40 expression', 'XPO:0101241', 'abnormal nucleate erythrocyte', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(464398, 'HP:0031384', 'Reduced T cell CD40 expression', 'XPO:0101435', 'abnormal paracrine cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(464399, 'HP:0031384', 'Reduced T cell CD40 expression', 'XPO:0100449', 'abnormal lymphocyte', 0.43333333333333335, 5.64885357140806, 1.5645563421015427, 'HP:0002715', 'Abnormality of the immune system'),
(464400, 'HP:0031384', 'Reduced T cell CD40 expression', 'XPO:0100540', 'abnormal left lymph heart', 0.41935483870967744, 5.64885357140806, 1.5391147060347428, 'HP:0002715', 'Abnormality of the immune system'),
(464401, 'HP:0031384', 'Reduced T cell CD40 expression', 'XPO:0100754', 'abnormal electrically active cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(464402, 'HP:0031384', 'Reduced T cell CD40 expression', 'XPO:0100108', 'abnormal cell part', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(464403, 'HP:0031384', 'Reduced T cell CD40 expression', 'XPO:0100638', 'abnormal polar body', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(464404, 'HP:0031384', 'Reduced T cell CD40 expression', 'XPO:0101083', 'abnormal T cell', 0.41935483870967744, 5.64885357140806, 1.5391147060347428, 'HP:0002715', 'Abnormality of the immune system'),
(464405, 'HP:0031384', 'Reduced T cell CD40 expression', 'XPO:0102213', 'abnormal immune system morphology', 0.4117647058823529, 5.64885357140806, 1.525122463739656, 'HP:0002715', 'Abnormality of the immune system'),
(464406, 'HP:0031384', 'Reduced T cell CD40 expression', 'XPO:0100549', 'abnormal mitotic cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(464407, 'HP:0031384', 'Reduced T cell CD40 expression', 'XPO:0100745', 'abnormal anterior lymph sac', 0.4482758620689655, 5.64885357140806, 1.5913028324062968, 'HP:0002715', 'Abnormality of the immune system'),
(464408, 'HP:0031384', 'Reduced T cell CD40 expression', 'XPO:0100285', 'abnormal progenitor cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(464409, 'HP:0031384', 'Reduced T cell CD40 expression', 'XPO:0101451', 'abnormal dorsal lymph space', 0.4642857142857143, 5.64885357140806, 1.6194696710023933, 'HP:0002715', 'Abnormality of the immune system'),
(464410, 'HP:0031384', 'Reduced T cell CD40 expression', 'XPO:0101221', 'abnormal larval immune system', 0.48148148148148145, 5.64885357140806, 1.6491871895674883, 'HP:0002715', 'Abnormality of the immune system'),
(464411, 'HP:0031384', 'Reduced T cell CD40 expression', 'XPO:0101864', 'abnormal lymphatic system morphology', 0.4117647058823529, 5.64885357140806, 1.525122463739656, 'HP:0002715', 'Abnormality of the immune system'),
(464412, 'HP:0031384', 'Reduced T cell CD40 expression', 'XPO:0101448', 'abnormal myelin accumulating cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(464413, 'HP:0031384', 'Reduced T cell CD40 expression', 'XPO:0141497', 'abnormal lymphoblast', 0.43333333333333335, 5.64885357140806, 1.5645563421015427, 'HP:0002715', 'Abnormality of the immune system'),
(464414, 'HP:0031384', 'Reduced T cell CD40 expression', 'XPO:0100791', 'abnormal multiciliated cell precursor', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(464415, 'HP:0031384', 'Reduced T cell CD40 expression', 'XPO:0100289', 'abnormal chondroblast', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(464416, 'HP:0031384', 'Reduced T cell CD40 expression', 'XPO:0100581', 'abnormal immune system', 0.5, 5.64885357140806, 1.6806031017774632, 'HP:0002715', 'Abnormality of the immune system'),
(464417, 'HP:0031384', 'Reduced T cell CD40 expression', 'XPO:0100852', 'abnormal interdigital region', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(464418, 'HP:0031384', 'Reduced T cell CD40 expression', 'XPO:0101029', 'abnormal right spleen primordium', 0.43333333333333335, 5.64885357140806, 1.5645563421015427, 'HP:0002715', 'Abnormality of the immune system'),
(464419, 'HP:0031384', 'Reduced T cell CD40 expression', 'XPO:0100004', 'abnormal cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(464420, 'HP:0031384', 'Reduced T cell CD40 expression', 'XPO:0101326', 'abnormal cementoblast', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(464421, 'HP:0031384', 'Reduced T cell CD40 expression', 'XPO:0141622', 'metaplastic right lymph heart', 0.4117647058823529, 5.64885357140806, 1.525122463739656, 'HP:0002715', 'Abnormality of the immune system'),
(464422, 'HP:0031384', 'Reduced T cell CD40 expression', 'XPO:0100653', 'abnormal myoblast', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(464423, 'HP:0031384', 'Reduced T cell CD40 expression', 'XPO:0103083', 'abnormal dorsal lymph space morphology', 0.4117647058823529, 5.64885357140806, 1.525122463739656, 'HP:0002715', 'Abnormality of the immune system'),
(464424, 'HP:0031384', 'Reduced T cell CD40 expression', 'XPO:0101518', 'abnormal B cell', 0.41935483870967744, 5.64885357140806, 1.5391147060347428, 'HP:0002715', 'Abnormality of the immune system'),
(464425, 'HP:0031384', 'Reduced T cell CD40 expression', 'XPO:0100337', 'abnormal zygote', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(464426, 'HP:0031384', 'Reduced T cell CD40 expression', 'XPO:0100006', 'abnormal anatomical structure', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(464427, 'HP:0031384', 'Reduced T cell CD40 expression', 'XPO:0100232', 'abnormal lymphatic system', 0.5, 5.64885357140806, 1.6806031017774632, 'HP:0002715', 'Abnormality of the immune system'),
(464428, 'HP:0031384', 'Reduced T cell CD40 expression', 'XPO:0100081', 'abnormal anatomical entity in vitro', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(464429, 'HP:0031384', 'Reduced T cell CD40 expression', 'XPO:0100242', 'abnormal right lymph heart', 0.41935483870967744, 5.64885357140806, 1.5391147060347428, 'HP:0002715', 'Abnormality of the immune system'),
(464430, 'HP:0031384', 'Reduced T cell CD40 expression', 'XPO:0100481', 'abnormal anatomical line', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(464431, 'HP:0031384', 'Reduced T cell CD40 expression', 'XPO:0100599', 'abnormal adult immune system', 0.48148148148148145, 5.64885357140806, 1.6491871895674883, 'HP:0002715', 'Abnormality of the immune system'),
(464432, 'HP:0031384', 'Reduced T cell CD40 expression', 'XPO:0100533', 'abnormal melanoblast', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(464433, 'HP:0031384', 'Reduced T cell CD40 expression', 'XPO:0100477', 'abnormal pericyte', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(464434, 'HP:0031384', 'Reduced T cell CD40 expression', 'XPO:0126559', 'abnormally localised lymphatic system', 0.4117647058823529, 5.64885357140806, 1.525122463739656, 'HP:0002715', 'Abnormality of the immune system'),
(464435, 'HP:0031384', 'Reduced T cell CD40 expression', 'XPO:0126677', 'abnormally localised dorsal lymph space', 0.4117647058823529, 5.64885357140806, 1.525122463739656, 'HP:0002715', 'Abnormality of the immune system'),
(464436, 'HP:0031384', 'Reduced T cell CD40 expression', 'XPO:0100026', 'abnormal germ cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(464437, 'HP:0031384', 'Reduced T cell CD40 expression', 'XPO:0101237', 'abnormal mucus secreting cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(464438, 'HP:0031384', 'Reduced T cell CD40 expression', 'XPO:0141616', 'metaplastic left lymph heart', 0.4117647058823529, 5.64885357140806, 1.525122463739656, 'HP:0002715', 'Abnormality of the immune system'),
(464439, 'HP:0031384', 'Reduced T cell CD40 expression', 'XPO:0100814', 'abnormal natural killer cell', 0.40625, 5.64885357140806, 1.5148751642906173, 'HP:0002715', 'Abnormality of the immune system'),
(464440, 'HP:0012564', 'Premature epimetaphyseal fusion in tibia', 'XPO:0140559', 'abnormally necrotic articular system', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(464441, 'HP:0012564', 'Premature epimetaphyseal fusion in tibia', 'XPO:0140432', 'abnormally necrotic skeleton', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(464442, 'HP:0012564', 'Premature epimetaphyseal fusion in tibia', 'XPO:0102010', 'abnormal perichondrium morphology', 0.4444444444444444, 4.638757693672553, 1.4358516936218344, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(464443, 'HP:0012564', 'Premature epimetaphyseal fusion in tibia', 'XPO:0102605', 'abnormal dermal skeleton morphology', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(464444, 'HP:0012564', 'Premature epimetaphyseal fusion in tibia', 'XPO:0102097', 'abnormal skeletal system morphology', 0.47619047619047616, 4.638757693672553, 1.4862477031377266, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(464445, 'HP:0012564', 'Premature epimetaphyseal fusion in tibia', 'XPO:0141703', 'abnormally necrotic posterior notochord', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(464446, 'HP:0012564', 'Premature epimetaphyseal fusion in tibia', 'XPO:0102130', 'abnormal endoskeleton morphology', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(464447, 'HP:0012564', 'Premature epimetaphyseal fusion in tibia', 'XPO:0102542', 'abnormal vacuolated notochordal tissue morphology', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(464448, 'HP:0012564', 'Premature epimetaphyseal fusion in tibia', 'XPO:0128352', 'decreased size of the skeletal system', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(464449, 'HP:0012564', 'Premature epimetaphyseal fusion in tibia', 'XPO:0102980', 'abnormal perichordal tissue morphology', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(464450, 'HP:0012564', 'Premature epimetaphyseal fusion in tibia', 'XPO:0140683', 'abnormally necrotic flexural organ', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(464451, 'HP:0012564', 'Premature epimetaphyseal fusion in tibia', 'XPO:0141719', 'abnormal anterior notochord morphology', 0.45454545454545453, 4.638757693672553, 1.452076521536181, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(464452, 'HP:0012564', 'Premature epimetaphyseal fusion in tibia', 'XPO:0102217', 'abnormal elastica externa morphology', 0.47619047619047616, 4.638757693672553, 1.4862477031377266, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(464453, 'HP:0012564', 'Premature epimetaphyseal fusion in tibia', 'XPO:0102567', 'abnormal skeleton morphology', 0.45454545454545453, 4.638757693672553, 1.452076521536181, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(464454, 'HP:0012564', 'Premature epimetaphyseal fusion in tibia', 'XPO:0139774', 'abnormally necrotic elastica externa', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(464455, 'HP:0012564', 'Premature epimetaphyseal fusion in tibia', 'XPO:0102054', 'abnormal notochord morphology', 0.45454545454545453, 4.638757693672553, 1.452076521536181, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(464456, 'HP:0012564', 'Premature epimetaphyseal fusion in tibia', 'XPO:0141723', 'abnormal posterior notochord morphology', 0.45454545454545453, 4.638757693672553, 1.452076521536181, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(464457, 'HP:0012564', 'Premature epimetaphyseal fusion in tibia', 'XPO:0128890', 'decreased size of the elastica externa', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(464458, 'HP:0012564', 'Premature epimetaphyseal fusion in tibia', 'XPO:0140019', 'abnormally necrotic skeletal system', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(464459, 'HP:0012564', 'Premature epimetaphyseal fusion in tibia', 'XPO:0101982', 'abnormal appendicular skeleton morphology', 0.46808510638297873, 5.732269579595698, 1.6380445708163638, 'HP:0011844', 'Abnormal appendicular skeleton morphology'),
(464460, 'HP:0012564', 'Premature epimetaphyseal fusion in tibia', 'XPO:0129832', 'increased size of the skeletal system', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(464461, 'HP:0012564', 'Premature epimetaphyseal fusion in tibia', 'XPO:0141699', 'abnormally necrotic anterior notochord', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(464462, 'HP:0012564', 'Premature epimetaphyseal fusion in tibia', 'XPO:0101755', 'abnormal pelvic girdle morphology', 0.43137254901960786, 5.732269579595698, 1.5724960223217586, 'HP:0011844', 'Abnormal appendicular skeleton morphology'),
(464463, 'HP:0012564', 'Premature epimetaphyseal fusion in tibia', 'XPO:0140177', 'abnormally necrotic appendicular skeleton', 0.41509433962264153, 5.732269579595698, 1.5425409737446956, 'HP:0011844', 'Abnormal appendicular skeleton morphology'),
(464464, 'HP:0012564', 'Premature epimetaphyseal fusion in tibia', 'XPO:0130368', 'increased size of the elastica externa', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(464465, 'HP:0012564', 'Premature epimetaphyseal fusion in tibia', 'XPO:0107372', 'abnormal flexural organ morphology', 0.45454545454545453, 4.638757693672553, 1.452076521536181, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(464466, 'HP:0012564', 'Premature epimetaphyseal fusion in tibia', 'XPO:0102514', 'abnormal perichondrial cell morphology', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(464467, 'HP:0012564', 'Premature epimetaphyseal fusion in tibia', 'XPO:0101860', 'abnormal skeletal subdivision morphology', 0.4444444444444444, 4.638757693672553, 1.4358516936218344, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(464468, 'HP:0012564', 'Premature epimetaphyseal fusion in tibia', 'XPO:0102144', 'abnormal cranial skeleton morphology', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(464469, 'HP:0012564', 'Premature epimetaphyseal fusion in tibia', 'XPO:0102806', 'abnormal articular system morphology', 0.46511627906976744, 4.638757693672553, 1.4688640910537754, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(464470, 'HP:0012564', 'Premature epimetaphyseal fusion in tibia', 'XPO:0140350', 'abnormally necrotic notochordal sheath', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(464471, 'HP:0012564', 'Premature epimetaphyseal fusion in tibia', 'XPO:0101957', 'abnormal axial skeleton morphology', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(464472, 'HP:0012564', 'Premature epimetaphyseal fusion in tibia', 'XPO:0102272', 'abnormal notochordal sheath morphology', 0.45454545454545453, 4.638757693672553, 1.452076521536181, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(464473, 'HP:0012564', 'Premature epimetaphyseal fusion in tibia', 'XPO:0100584', 'abnormal vertebral column', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(464474, 'HP:0100360', 'Upper-limb joint contracture', 'XPO:0128816', 'decreased size of the tendon', 0.4057971014492754, 10.802658907487096, 2.0937257873473927, 'UPHENO:0021425', 'abnormal tendon morphology'),
(464475, 'HP:0410063', 'Increased level of galactonate in red blood cells', 'XPO:0141917', 'abnormal tryptophan metabolic process', 0.5384615384615384, 9.119292702704945, 2.2159396152376503, 'HP:0004354', 'Abnormal circulating carboxylic acid concentration'),
(464476, 'HP:0410063', 'Increased level of galactonate in red blood cells', 'XPO:0141868', 'abnormal asparagine metabolic process', 0.5384615384615384, 9.119292702704945, 2.2159396152376503, 'HP:0004354', 'Abnormal circulating carboxylic acid concentration'),
(464477, 'HP:0410063', 'Increased level of galactonate in red blood cells', 'XPO:0141882', 'abnormal gamma-aminobutyric acid metabolic process', 0.5555555555555556, 9.119292702704945, 2.250838449050702, 'HP:0004354', 'Abnormal circulating carboxylic acid concentration'),
(464478, 'HP:0410063', 'Increased level of galactonate in red blood cells', 'XPO:0141896', 'abnormal lysine metabolic process', 0.5384615384615384, 9.119292702704945, 2.2159396152376503, 'HP:0004354', 'Abnormal circulating carboxylic acid concentration'),
(464479, 'HP:0410063', 'Increased level of galactonate in red blood cells', 'XPO:0141857', 'abnormal glycine metabolic process', 0.5303030303030303, 9.119292702704945, 2.199088118849434, 'HP:0004354', 'Abnormal circulating carboxylic acid concentration'),
(464480, 'HP:0410063', 'Increased level of galactonate in red blood cells', 'XPO:0141847', 'abnormal arginine metabolic process', 0.5384615384615384, 9.119292702704945, 2.2159396152376503, 'HP:0004354', 'Abnormal circulating carboxylic acid concentration'),
(464481, 'HP:0410063', 'Increased level of galactonate in red blood cells', 'XPO:0141888', 'abnormal threonine metabolic process', 0.5384615384615384, 9.119292702704945, 2.2159396152376503, 'HP:0004354', 'Abnormal circulating carboxylic acid concentration'),
(464482, 'HP:0410063', 'Increased level of galactonate in red blood cells', 'XPO:0141912', 'abnormal D-serine metabolic process', 0.5303030303030303, 9.119292702704945, 2.199088118849434, 'HP:0004354', 'Abnormal circulating carboxylic acid concentration'),
(464483, 'HP:0410063', 'Increased level of galactonate in red blood cells', 'XPO:0141918', 'abnormal tyrosine metabolic process', 0.5384615384615384, 9.119292702704945, 2.2159396152376503, 'HP:0004354', 'Abnormal circulating carboxylic acid concentration'),
(464484, 'HP:0410063', 'Increased level of galactonate in red blood cells', 'XPO:0141895', 'abnormal leucine metabolic process', 0.5384615384615384, 9.119292702704945, 2.2159396152376503, 'HP:0004354', 'Abnormal circulating carboxylic acid concentration'),
(464485, 'HP:0410063', 'Increased level of galactonate in red blood cells', 'XPO:0141853', 'abnormal glutamate metabolic process', 0.5223880597014925, 9.119292702704945, 2.1826153167280795, 'HP:0004354', 'Abnormal circulating carboxylic acid concentration'),
(464486, 'HP:0410063', 'Increased level of galactonate in red blood cells', 'XPO:0141893', 'abnormal isoleucine metabolic process', 0.5384615384615384, 9.119292702704945, 2.2159396152376503, 'HP:0004354', 'Abnormal circulating carboxylic acid concentration'),
(464487, 'HP:0410063', 'Increased level of galactonate in red blood cells', 'XPO:0141889', 'abnormal homoserine metabolic process', 0.5303030303030303, 9.119292702704945, 2.199088118849434, 'HP:0004354', 'Abnormal circulating carboxylic acid concentration'),
(464488, 'HP:0410063', 'Increased level of galactonate in red blood cells', 'XPO:0141913', 'abnormal L-serine metabolic process', 0.5303030303030303, 9.119292702704945, 2.199088118849434, 'HP:0004354', 'Abnormal circulating carboxylic acid concentration'),
(464489, 'HP:0410063', 'Increased level of galactonate in red blood cells', 'XPO:0141905', 'abnormal ornithine metabolic process', 0.546875, 9.119292702704945, 2.2331845415889315, 'HP:0004354', 'Abnormal circulating carboxylic acid concentration'),
(464490, 'HP:0410063', 'Increased level of galactonate in red blood cells', 'XPO:0141887', 'abnormal histidine metabolic process', 0.5384615384615384, 9.119292702704945, 2.2159396152376503, 'HP:0004354', 'Abnormal circulating carboxylic acid concentration'),
(464491, 'HP:0410063', 'Increased level of galactonate in red blood cells', 'XPO:0141858', 'abnormal serine family amino acid metabolic process', 0.546875, 9.119292702704945, 2.2331845415889315, 'HP:0004354', 'Abnormal circulating carboxylic acid concentration'),
(464492, 'HP:0410063', 'Increased level of galactonate in red blood cells', 'XPO:0141873', 'abnormal tricarboxylic acid metabolic process', 0.603448275862069, 9.119292702704945, 2.3458519685881387, 'HP:0004354', 'Abnormal circulating carboxylic acid concentration'),
(464493, 'HP:0410063', 'Increased level of galactonate in red blood cells', 'XPO:0141922', 'abnormal valine metabolic process', 0.5384615384615384, 9.119292702704945, 2.2159396152376503, 'HP:0004354', 'Abnormal circulating carboxylic acid concentration'),
(464494, 'HP:0410063', 'Increased level of galactonate in red blood cells', 'XPO:0141869', 'abnormal alpha-amino acid metabolic process', 0.5645161290322581, 9.119292702704945, 2.2689177631732522, 'HP:0004354', 'Abnormal circulating carboxylic acid concentration'),
(464495, 'HP:0410063', 'Increased level of galactonate in red blood cells', 'XPO:0141848', 'abnormal proline metabolic process', 0.5384615384615384, 9.119292702704945, 2.2159396152376503, 'HP:0004354', 'Abnormal circulating carboxylic acid concentration'),
(464496, 'HP:0410063', 'Increased level of galactonate in red blood cells', 'XPO:0141843', 'abnormal alanine metabolic process', 0.546875, 9.119292702704945, 2.2331845415889315, 'HP:0004354', 'Abnormal circulating carboxylic acid concentration'),
(464497, 'HP:0003029', 'Enlargement of the ankles', 'XPO:0141559', 'abnormal tarsus morphology in the regenerating hindlimb', 0.4431818181818182, 11.854497839006713, 2.292094654660542, 'UPHENO:0088165', 'abnormal tarsal region morphology'),
(464498, 'HP:0003029', 'Enlargement of the ankles', 'XPO:0130219', 'increased size of the interdigital region', 0.42592592592592593, 6.173473740856008, 1.6215555862360949, 'UPHENO:0087006', 'abnormal autopod region morphology'),
(464499, 'HP:0003029', 'Enlargement of the ankles', 'XPO:0129337', 'decreased size of the tarsus', 0.43010752688172044, 11.854497839006713, 2.258032052022264, 'UPHENO:0088165', 'abnormal tarsal region morphology'),
(464500, 'HP:0003029', 'Enlargement of the ankles', 'XPO:0130812', 'increased size of the tarsus', 0.4666666666666667, 11.854497839006713, 2.3520414519171355, 'UPHENO:0088165', 'abnormal tarsal region morphology'),
(464501, 'HP:0003029', 'Enlargement of the ankles', 'XPO:0133380', 'fused tarsi part of regenerating hindlimb', 0.42391304347826086, 11.854497839006713, 2.241712795573912, 'UPHENO:0088165', 'abnormal tarsal region morphology'),
(464502, 'HP:0003029', 'Enlargement of the ankles', 'XPO:0133361', 'fused tarsi', 0.4588235294117647, 11.854497839006713, 2.332192645965851, 'UPHENO:0088165', 'abnormal tarsal region morphology'),
(464503, 'HP:0003029', 'Enlargement of the ankles', 'XPO:0140332', 'abnormally necrotic tarsus', 0.42857142857142855, 11.854497839006713, 2.253996245307436, 'UPHENO:0088165', 'abnormal tarsal region morphology'),
(464504, 'HP:0003029', 'Enlargement of the ankles', 'XPO:0103578', 'decreased length of tarsus', 0.41237113402061853, 11.854497839006713, 2.210984558316989, 'UPHENO:0088165', 'abnormal tarsal region morphology'),
(464505, 'HP:0003029', 'Enlargement of the ankles', 'XPO:0141551', 'abnormal joint morphology in the tarsus', 0.4431818181818182, 11.854497839006713, 2.292094654660542, 'UPHENO:0088165', 'abnormal tarsal region morphology'),
(464506, 'HP:0003029', 'Enlargement of the ankles', 'XPO:0103072', 'abnormal tarsus morphology', 0.47560975609756095, 11.854497839006713, 2.3744714834819654, 'UPHENO:0088165', 'abnormal tarsal region morphology'),
(464507, 'HP:0031179', 'Nuchal rigidity', 'XPO:0100574', 'abnormal gastrula cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(464508, 'HP:0031179', 'Nuchal rigidity', 'XPO:0100727', 'abnormal odontogenic papilla', 0.4642857142857143, 3.8539481361839503, 1.3376595468310548, 'UPHENO:0002764', 'abnormal craniocervical region'),
(464509, 'HP:0031179', 'Nuchal rigidity', 'XPO:0141315', 'abnormal anatomical region', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(464510, 'HP:0031179', 'Nuchal rigidity', 'XPO:0100956', 'abnormal centrosome', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(464511, 'HP:0031179', 'Nuchal rigidity', 'XPO:0101237', 'abnormal mucus secreting cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(464512, 'HP:0031179', 'Nuchal rigidity', 'XPO:0100545', 'abnormal male organism', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(464513, 'HP:0031179', 'Nuchal rigidity', 'XPO:00000000', 'Xenopus phenotype', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(464514, 'HP:0031179', 'Nuchal rigidity', 'XPO:0100533', 'abnormal melanoblast', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(464515, 'HP:0031179', 'Nuchal rigidity', 'XPO:0100010', 'abnormal multicellular anatomical structure', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(464516, 'HP:0031179', 'Nuchal rigidity', 'XPO:0100392', 'abnormal cilium', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(464517, 'HP:0031179', 'Nuchal rigidity', 'XPO:0100976', 'abnormal multiciliated cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(464518, 'HP:0031179', 'Nuchal rigidity', 'XPO:0101221', 'abnormal larval immune system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(464519, 'HP:0031179', 'Nuchal rigidity', 'XPO:0101480', 'abnormal stage V oocyte', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(464520, 'HP:0031179', 'Nuchal rigidity', 'XPO:0100626', 'abnormal primordial germ cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(464521, 'HP:0031179', 'Nuchal rigidity', 'XPO:0101461', 'abnormal sperm entry point', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(464522, 'HP:0031179', 'Nuchal rigidity', 'XPO:0101061', 'abnormal plasma membrane', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(464523, 'HP:0031179', 'Nuchal rigidity', 'XPO:0100917', 'abnormal stage III oocyte', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(464524, 'HP:0031179', 'Nuchal rigidity', 'XPO:0100389', 'abnormal cranial placode', 0.40625, 3.8539481361839503, 1.2512659310972747, 'UPHENO:0002764', 'abnormal craniocervical region'),
(464525, 'HP:0031179', 'Nuchal rigidity', 'XPO:0131678', 'abnormal intercanthal region', 0.41935483870967744, 3.8539481361839503, 1.271287457282924, 'UPHENO:0002764', 'abnormal craniocervical region'),
(464526, 'HP:0031179', 'Nuchal rigidity', 'XPO:0100791', 'abnormal multiciliated cell precursor', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(464527, 'HP:0031179', 'Nuchal rigidity', 'XPO:0100653', 'abnormal myoblast', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(464528, 'HP:0031179', 'Nuchal rigidity', 'XPO:0131656', 'abnormal periocular mesenchyme', 0.40625, 3.8539481361839503, 1.2512659310972747, 'UPHENO:0002764', 'abnormal craniocervical region'),
(464529, 'HP:0031179', 'Nuchal rigidity', 'XPO:0101333', 'abnormal barrier epithelial cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(464530, 'HP:0031179', 'Nuchal rigidity', 'XPO:0100372', 'abnormal hematological system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(464531, 'HP:0031179', 'Nuchal rigidity', 'XPO:0101220', 'abnormal centriole', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(464532, 'HP:0031179', 'Nuchal rigidity', 'XPO:0131675', 'abnormal spindle microtubule', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(464533, 'HP:0031179', 'Nuchal rigidity', 'XPO:0100664', 'abnormal periocular region', 0.4482758620689655, 3.8539481361839503, 1.3143941277702602, 'UPHENO:0002764', 'abnormal craniocervical region'),
(464534, 'HP:0031179', 'Nuchal rigidity', 'XPO:0142052', 'abnormal nasal region', 0.48148148148148145, 3.8539481361839503, 1.362205806096363, 'UPHENO:0002764', 'abnormal craniocervical region'),
(464535, 'HP:0031179', 'Nuchal rigidity', 'XPO:0100437', 'abnormal proepicardium', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(464536, 'HP:0031179', 'Nuchal rigidity', 'XPO:0107270', 'abnormal proximal-distal axis', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(464537, 'HP:0031179', 'Nuchal rigidity', 'XPO:0115512', 'abnormally semi-erect whole organism', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(464538, 'HP:0031179', 'Nuchal rigidity', 'XPO:0100004', 'abnormal cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(464539, 'HP:0031179', 'Nuchal rigidity', 'XPO:0100337', 'abnormal zygote', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(464540, 'HP:0031179', 'Nuchal rigidity', 'XPO:0100344', 'abnormal portion of organism substance', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(464541, 'HP:0031179', 'Nuchal rigidity', 'XPO:0101513', 'abnormal basal body', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(464542, 'HP:0031179', 'Nuchal rigidity', 'XPO:0100549', 'abnormal mitotic cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(464543, 'HP:0031179', 'Nuchal rigidity', 'XPO:0100006', 'abnormal anatomical structure', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(464544, 'HP:0031179', 'Nuchal rigidity', 'XPO:0100025', 'abnormal oocyte', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(464545, 'HP:0031179', 'Nuchal rigidity', 'XPO:0100907', 'abnormal cytoplasm', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(464546, 'HP:0031179', 'Nuchal rigidity', 'XPO:0100108', 'abnormal cell part', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(464547, 'HP:0031179', 'Nuchal rigidity', 'XPO:0100715', 'abnormal ciliated cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(464548, 'HP:0031179', 'Nuchal rigidity', 'XPO:0100899', 'abnormal secondary spermatogonium', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(464549, 'HP:0031179', 'Nuchal rigidity', 'XPO:0101241', 'abnormal nucleate erythrocyte', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(464550, 'HP:0031179', 'Nuchal rigidity', 'XPO:0100450', 'abnormal circumpharyngeal ridge', 0.41935483870967744, 3.8539481361839503, 1.271287457282924, 'UPHENO:0002764', 'abnormal craniocervical region'),
(464551, 'HP:0031179', 'Nuchal rigidity', 'XPO:0100317', 'abnormal respiratory system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(464552, 'HP:0031179', 'Nuchal rigidity', 'XPO:0100674', 'abnormal secondary oogonium', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(464553, 'HP:0031179', 'Nuchal rigidity', 'XPO:0101157', 'abnormal female organism', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(464554, 'HP:0031179', 'Nuchal rigidity', 'XPO:0101071', 'abnormal endoplasmic reticulum', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(464555, 'HP:0031179', 'Nuchal rigidity', 'XPO:0100599', 'abnormal adult immune system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(464556, 'HP:0031179', 'Nuchal rigidity', 'XPO:0100429', 'abnormal spermatid', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(464557, 'HP:0031179', 'Nuchal rigidity', 'XPO:0100894', 'abnormal nucleus', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(464558, 'HP:0031179', 'Nuchal rigidity', 'XPO:0142057', 'abnormal desmosome', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(464559, 'HP:0031179', 'Nuchal rigidity', 'XPO:0100691', 'abnormal keratin accumulating cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(464560, 'HP:0031179', 'Nuchal rigidity', 'XPO:0101297', 'abnormal barrier cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(464561, 'HP:0031179', 'Nuchal rigidity', 'XPO:0100906', 'abnormal lateral nasal prominence', 0.43333333333333335, 3.8539481361839503, 1.2923018967510567, 'UPHENO:0002764', 'abnormal craniocervical region'),
(464562, 'HP:0031179', 'Nuchal rigidity', 'XPO:0100477', 'abnormal pericyte', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(464563, 'HP:0031179', 'Nuchal rigidity', 'XPO:0100940', 'abnormal hatching gland primordium', 0.41935483870967744, 3.8539481361839503, 1.271287457282924, 'UPHENO:0002764', 'abnormal craniocervical region'),
(464564, 'HP:0031179', 'Nuchal rigidity', 'XPO:0100724', 'abnormal kinetochore', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(464565, 'HP:0031179', 'Nuchal rigidity', 'XPO:0100585', 'abnormal elastica externa', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(464566, 'HP:0031179', 'Nuchal rigidity', 'XPO:0100062', 'abnormal anatomical space', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(464567, 'HP:0031179', 'Nuchal rigidity', 'XPO:0107262', 'abnormal left-right axis', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(464568, 'HP:0031179', 'Nuchal rigidity', 'XPO:0100704', 'abnormal Merkel cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(464569, 'HP:0031179', 'Nuchal rigidity', 'XPO:0100084', 'abnormal anatomical group', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(464570, 'HP:0031179', 'Nuchal rigidity', 'XPO:0101172', 'abnormal pharyngeal pouch', 0.43333333333333335, 3.8539481361839503, 1.2923018967510567, 'UPHENO:0002764', 'abnormal craniocervical region'),
(464571, 'HP:0031179', 'Nuchal rigidity', 'XPO:0100386', 'abnormal limb', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(464572, 'HP:0031179', 'Nuchal rigidity', 'XPO:0101547', 'abnormal lampbrush chromosome', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(464573, 'HP:0031179', 'Nuchal rigidity', 'XPO:0100377', 'abnormal connective tissue', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(464574, 'HP:0031179', 'Nuchal rigidity', 'XPO:0131677', 'abnormal actin filament', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(464575, 'HP:0031179', 'Nuchal rigidity', 'XPO:0100308', 'abnormal early embryonic cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(464576, 'HP:0031179', 'Nuchal rigidity', 'XPO:0101468', 'abnormal stage I oocyte', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(464577, 'HP:0031179', 'Nuchal rigidity', 'XPO:0100176', 'abnormal stage VI oocyte', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(464578, 'HP:0031179', 'Nuchal rigidity', 'XPO:0100026', 'abnormal germ cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(464579, 'HP:0031179', 'Nuchal rigidity', 'XPO:0100638', 'abnormal polar body', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(464580, 'HP:0031179', 'Nuchal rigidity', 'XPO:0101409', 'abnormal perivitelline space', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(464581, 'HP:0031179', 'Nuchal rigidity', 'XPO:0100969', 'abnormal disaggregated/reaggregated ectoderm treated with activin', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(464582, 'HP:0031179', 'Nuchal rigidity', 'XPO:0101240', 'abnormal ciliated non-epidermal cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(464583, 'HP:0031179', 'Nuchal rigidity', 'XPO:0100285', 'abnormal progenitor cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(464584, 'HP:0031179', 'Nuchal rigidity', 'XPO:0101264', 'abnormal mitotic spindle', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(464585, 'HP:0031179', 'Nuchal rigidity', 'XPO:0100081', 'abnormal anatomical entity in vitro', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(464586, 'HP:0031179', 'Nuchal rigidity', 'XPO:0101435', 'abnormal paracrine cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(464587, 'HP:0031179', 'Nuchal rigidity', 'XPO:0100852', 'abnormal interdigital region', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(464588, 'HP:0031179', 'Nuchal rigidity', 'XPO:0101110', 'abnormal cell-free extract', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(464589, 'HP:0031179', 'Nuchal rigidity', 'XPO:0100258', 'abnormal organ part', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(464590, 'HP:0031179', 'Nuchal rigidity', 'XPO:0100232', 'abnormal lymphatic system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(464591, 'HP:0031179', 'Nuchal rigidity', 'XPO:0100307', 'abnormal blastomere', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(464592, 'HP:0031179', 'Nuchal rigidity', 'XPO:0100274', 'abnormal sensory system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(464593, 'HP:0031179', 'Nuchal rigidity', 'XPO:0100031', 'abnormal central nervous system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(464594, 'HP:0031179', 'Nuchal rigidity', 'XPO:0107258', 'abnormal anatomical axis', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(464595, 'HP:0031179', 'Nuchal rigidity', 'XPO:0115508', 'abnormally peramorphic growth of whole organism', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(464596, 'HP:0031179', 'Nuchal rigidity', 'XPO:0131667', 'abnormal actin cytoskeleton', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(464597, 'HP:0031179', 'Nuchal rigidity', 'XPO:0101569', 'abnormal activin-induced ectoderm', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(464598, 'HP:0031179', 'Nuchal rigidity', 'XPO:0107261', 'abnormal dorsal-ventral axis', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(464599, 'HP:0031179', 'Nuchal rigidity', 'XPO:0100546', 'abnormal whole organism', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(464600, 'HP:0031179', 'Nuchal rigidity', 'XPO:0100501', 'abnormal urogenital system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(464601, 'HP:0031179', 'Nuchal rigidity', 'XPO:0100515', 'abnormal somatic stem cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(464602, 'HP:0031179', 'Nuchal rigidity', 'XPO:0107312', 'abnormal filopodium', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(464603, 'HP:0031179', 'Nuchal rigidity', 'XPO:0100002', 'abnormal head', 0.48148148148148145, 3.8539481361839503, 1.362205806096363, 'UPHENO:0002764', 'abnormal craniocervical region'),
(464604, 'HP:0031179', 'Nuchal rigidity', 'XPO:0101113', 'abnormal stage IV oocyte', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(464605, 'HP:0031179', 'Nuchal rigidity', 'XPO:0101535', 'abnormal absorptive cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(464606, 'HP:0031179', 'Nuchal rigidity', 'XPO:0101109', 'abnormal egg cell-free extract', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(464607, 'HP:0031179', 'Nuchal rigidity', 'XPO:0100481', 'abnormal anatomical line', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(464608, 'HP:0031179', 'Nuchal rigidity', 'XPO:0100172', 'abnormal stem cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(464609, 'HP:0031179', 'Nuchal rigidity', 'XPO:0101472', 'abnormal zygote cortex', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(464610, 'HP:0031179', 'Nuchal rigidity', 'XPO:0100888', 'abnormal microtubule', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(464611, 'HP:0031179', 'Nuchal rigidity', 'XPO:0107260', 'abnormal anterior-posterior axis', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(464612, 'HP:0031179', 'Nuchal rigidity', 'XPO:0101228', 'abnormal mesenchymal stem cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(464613, 'HP:0031179', 'Nuchal rigidity', 'XPO:0101469', 'abnormal medial nasal prominence', 0.43333333333333335, 3.8539481361839503, 1.2923018967510567, 'UPHENO:0002764', 'abnormal craniocervical region'),
(464614, 'HP:0031179', 'Nuchal rigidity', 'XPO:0101373', 'abnormal oxygen accumulating cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(464615, 'HP:0031179', 'Nuchal rigidity', 'XPO:0141776', 'abnormal metabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(464616, 'HP:0031179', 'Nuchal rigidity', 'XPO:0107253', 'abnormal enteric nervous system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(464617, 'HP:0031179', 'Nuchal rigidity', 'XPO:0107259', 'abnormal animal-vegetal axis', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(464618, 'HP:0031179', 'Nuchal rigidity', 'XPO:0100032', 'abnormal nervous system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(464619, 'HP:0031179', 'Nuchal rigidity', 'XPO:0100573', 'abnormal extraembryonic structure', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(464620, 'HP:0031179', 'Nuchal rigidity', 'XPO:0101498', 'abnormal stage II oocyte', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(464621, 'HP:0031179', 'Nuchal rigidity', 'XPO:0100451', 'abnormal head mesenchyme', 0.43333333333333335, 3.8539481361839503, 1.2923018967510567, 'UPHENO:0002764', 'abnormal craniocervical region'),
(464622, 'HP:0031179', 'Nuchal rigidity', 'XPO:0100289', 'abnormal chondroblast', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(464623, 'HP:0031179', 'Nuchal rigidity', 'XPO:0100687', 'abnormal periotic region', 0.4482758620689655, 3.8539481361839503, 1.3143941277702602, 'UPHENO:0002764', 'abnormal craniocervical region'),
(464624, 'HP:0031179', 'Nuchal rigidity', 'XPO:0100721', 'abnormal centromere', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(464625, 'HP:0031179', 'Nuchal rigidity', 'XPO:0131685', 'abnormal cortical actin cytoskeleton', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(464626, 'HP:0031179', 'Nuchal rigidity', 'XPO:0100423', 'abnormal process', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(464627, 'HP:0031179', 'Nuchal rigidity', 'XPO:0107284', 'abnormal migrating myoblast', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(464628, 'HP:0031179', 'Nuchal rigidity', 'XPO:0100754', 'abnormal electrically active cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(464629, 'HP:0031179', 'Nuchal rigidity', 'XPO:0100202', 'abnormal embryo', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(464630, 'HP:0031179', 'Nuchal rigidity', 'XPO:0100902', 'abnormal spermatocyte', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(464631, 'HP:0031179', 'Nuchal rigidity', 'XPO:0101467', 'abnormal alkali secreting cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(464632, 'HP:0031179', 'Nuchal rigidity', 'XPO:0100802', 'abnormal exocrine cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(464633, 'HP:0031179', 'Nuchal rigidity', 'XPO:0100581', 'abnormal immune system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(464634, 'HP:0031179', 'Nuchal rigidity', 'XPO:0101402', 'abnormal oropharyngeal papilla', 0.4482758620689655, 3.8539481361839503, 1.3143941277702602, 'UPHENO:0002764', 'abnormal craniocervical region'),
(464635, 'HP:0031179', 'Nuchal rigidity', 'XPO:0101448', 'abnormal myelin accumulating cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(464636, 'HP:0031179', 'Nuchal rigidity', 'XPO:0100728', 'abnormal cell condensation', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(464637, 'HP:0031179', 'Nuchal rigidity', 'XPO:0100225', 'abnormal endocrine system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(464638, 'HP:0031179', 'Nuchal rigidity', 'XPO:0115509', 'abnormally semi-viable whole organism', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(464639, 'HP:0031179', 'Nuchal rigidity', 'XPO:0101141', 'abnormal Keller explant', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(464640, 'HP:0031179', 'Nuchal rigidity', 'XPO:0141499', 'abnormal tadpole', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(464641, 'HP:0031179', 'Nuchal rigidity', 'XPO:0101132', 'abnormal apoptotic cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(464642, 'HP:0031179', 'Nuchal rigidity', 'XPO:0101102', 'abnormal craniofacial region', 0.43333333333333335, 3.8539481361839503, 1.2923018967510567, 'UPHENO:0002764', 'abnormal craniocervical region'),
(464643, 'HP:0031179', 'Nuchal rigidity', 'XPO:0115505', 'dead whole organism', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(464644, 'HP:0031179', 'Nuchal rigidity', 'XPO:0101326', 'abnormal cementoblast', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(464645, 'HP:0031179', 'Nuchal rigidity', 'XPO:0131666', 'abnormal adherens junction', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(464646, 'HP:0031179', 'Nuchal rigidity', 'XPO:0100239', 'abnormal acellular anatomical structure', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(464647, 'HP:0031179', 'Nuchal rigidity', 'XPO:0100627', 'abnormal pharyngeal region', 0.4642857142857143, 3.8539481361839503, 1.3376595468310548, 'UPHENO:0002764', 'abnormal craniocervical region'),
(464648, 'HP:0031179', 'Nuchal rigidity', 'XPO:0101366', 'abnormal morula cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(464649, 'HP:0031179', 'Nuchal rigidity', 'XPO:0101004', 'abnormal acid secreting cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(464650, 'HP:0031925', 'Rosette', 'XPO:0140169', 'abnormally necrotic stage VI oocyte', 0.47368421052631576, 5.43643956286526, 1.6047291305419304, 'HP:0025461', 'Abnormal cell morphology'),
(464651, 'HP:0031925', 'Rosette', 'XPO:0102360', 'abnormal cell condensation morphology', 0.46153846153846156, 2.7446671847279203, 1.125508538339192, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(464652, 'HP:0031925', 'Rosette', 'XPO:0131032', 'abnormally increased number of acid secreting cell', 0.42424242424242425, 3.6715585125471644, 1.2480508339450433, 'UPHENO:0086172', 'abnormal cell'),
(464653, 'HP:0031925', 'Rosette', 'XPO:0101079', 'abnormal blastomere D1.1.2', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(464654, 'HP:0031925', 'Rosette', 'XPO:0131627', 'increased size of the actin cytoskeleton', 0.45714285714285713, 3.6715585125471644, 1.2955411026258445, 'UPHENO:0086172', 'abnormal cell'),
(464655, 'HP:0031925', 'Rosette', 'XPO:0100676', 'abnormal blastomere D2.2', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(464656, 'HP:0031925', 'Rosette', 'XPO:0101311', 'abnormal bottle cell', 0.48148148148148145, 3.6715585125471644, 1.3295816755533123, 'UPHENO:0086172', 'abnormal cell'),
(464657, 'HP:0031925', 'Rosette', 'XPO:0140366', 'abnormally necrotic left-ventral blastomere', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(464658, 'HP:0031925', 'Rosette', 'XPO:0101848', 'abnormal hepato-pancreatic progenitor cell morphology', 0.4090909090909091, 5.43643956286526, 1.491307481034791, 'HP:0025461', 'Abnormal cell morphology'),
(464659, 'HP:0031925', 'Rosette', 'XPO:0129408', 'decreased size of the exocrine cell', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(464660, 'HP:0031925', 'Rosette', 'XPO:0102739', 'abnormal erythroid cell morphology', 0.5294117647058824, 5.43643956286526, 1.696500828969256, 'HP:0025461', 'Abnormal cell morphology'),
(464661, 'HP:0031925', 'Rosette', 'XPO:0141497', 'abnormal lymphoblast', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(464662, 'HP:0031925', 'Rosette', 'XPO:0102586', 'abnormal neural progenitor cell morphology', 0.4864864864864865, 5.43643956286526, 1.626270082715184, 'HP:0025461', 'Abnormal cell morphology'),
(464663, 'HP:0031925', 'Rosette', 'XPO:0102228', 'abnormal myocyte morphology', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(464664, 'HP:0031925', 'Rosette', 'XPO:0102824', 'abnormal blastomere D2.1 morphology', 0.43902439024390244, 5.43643956286526, 1.5449043867452603, 'HP:0025461', 'Abnormal cell morphology'),
(464665, 'HP:0031925', 'Rosette', 'XPO:0102715', 'abnormal T cell morphology', 0.5, 5.43643956286526, 1.6487024538808177, 'HP:0025461', 'Abnormal cell morphology'),
(464666, 'HP:0031925', 'Rosette', 'XPO:0102183', 'abnormal oocyte cortex morphology', 0.5161290322580645, 3.6715585125471644, 1.376589242279565, 'UPHENO:0086172', 'abnormal cell'),
(464667, 'HP:0031925', 'Rosette', 'XPO:0131706', 'abnormal ciliary basal body organization', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(464668, 'HP:0031925', 'Rosette', 'XPO:0107410', 'abnormal thrombocyte morphology', 0.42857142857142855, 5.43643956286526, 1.526401870347189, 'HP:0025461', 'Abnormal cell morphology'),
(464669, 'HP:0031925', 'Rosette', 'XPO:0107426', 'abnormal yolk platelet morphology', 0.5161290322580645, 3.6715585125471644, 1.376589242279565, 'UPHENO:0086172', 'abnormal cell'),
(464670, 'HP:0031925', 'Rosette', 'XPO:0140610', 'abnormally necrotic blastomere D1', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(464671, 'HP:0031925', 'Rosette', 'XPO:0130833', 'increased size of the filopodium', 0.45714285714285713, 3.6715585125471644, 1.2955411026258445, 'UPHENO:0086172', 'abnormal cell'),
(464672, 'HP:0031925', 'Rosette', 'XPO:0139841', 'abnormally necrotic anatomical region', 0.4444444444444444, 2.7446671847279203, 1.104469140402437, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(464673, 'HP:0031925', 'Rosette', 'XPO:0102768', 'abnormal ooplasm morphology', 0.5161290322580645, 3.6715585125471644, 1.376589242279565, 'UPHENO:0086172', 'abnormal cell'),
(464674, 'HP:0031925', 'Rosette', 'XPO:0131082', 'abnormally increased number of alkali secreting cell', 0.42424242424242425, 3.6715585125471644, 1.2480508339450433, 'UPHENO:0086172', 'abnormal cell'),
(464675, 'HP:0031925', 'Rosette', 'XPO:0131136', 'abnormally increased number of multiciliated cell precursor', 0.42424242424242425, 3.6715585125471644, 1.2480508339450433, 'UPHENO:0086172', 'abnormal cell'),
(464676, 'HP:0031925', 'Rosette', 'XPO:0102959', 'abnormal blastomere V1.2.1 morphology', 0.43902439024390244, 5.43643956286526, 1.5449043867452603, 'HP:0025461', 'Abnormal cell morphology'),
(464677, 'HP:0031925', 'Rosette', 'XPO:0102308', 'abnormal blastomere D2.2 morphology', 0.43902439024390244, 5.43643956286526, 1.5449043867452603, 'HP:0025461', 'Abnormal cell morphology'),
(464678, 'HP:0031925', 'Rosette', 'XPO:0140095', 'abnormally necrotic bottle cell', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(464679, 'HP:0031925', 'Rosette', 'XPO:0127806', 'abnormally localised spermatid', 0.42424242424242425, 3.6715585125471644, 1.2480508339450433, 'UPHENO:0086172', 'abnormal cell'),
(464680, 'HP:0031925', 'Rosette', 'XPO:0101716', 'abnormal anatomical group morphology', 0.46153846153846156, 2.7446671847279203, 1.125508538339192, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(464681, 'HP:0031925', 'Rosette', 'XPO:0125384', 'absent ciliated cell', 0.42424242424242425, 3.6715585125471644, 1.2480508339450433, 'UPHENO:0086172', 'abnormal cell'),
(464682, 'HP:0031925', 'Rosette', 'XPO:0139981', 'abnormally necrotic early embryonic cell', 0.5294117647058824, 5.43643956286526, 1.696500828969256, 'HP:0025461', 'Abnormal cell morphology'),
(464683, 'HP:0031925', 'Rosette', 'XPO:0140709', 'abnormally necrotic acid secreting cell', 0.5625, 5.43643956286526, 1.748713027947041, 'HP:0025461', 'Abnormal cell morphology'),
(464684, 'HP:0031925', 'Rosette', 'XPO:0129452', 'decreased size of the ring structure', 0.43243243243243246, 3.6715585125471644, 1.2600400701560144, 'UPHENO:0086172', 'abnormal cell'),
(464685, 'HP:0031925', 'Rosette', 'XPO:0131667', 'abnormal actin cytoskeleton', 0.52, 3.6715585125471644, 1.3817418089225373, 'UPHENO:0086172', 'abnormal cell'),
(464686, 'HP:0031925', 'Rosette', 'XPO:0130483', 'increased size of the myelin accumulating cell', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(464687, 'HP:0031925', 'Rosette', 'XPO:0131189', 'abnormally decreased number of stem cell', 0.4117647058823529, 3.6715585125471644, 1.229560169755361, 'UPHENO:0086172', 'abnormal cell'),
(464688, 'HP:0031925', 'Rosette', 'XPO:0101448', 'abnormal myelin accumulating cell', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(464689, 'HP:0031925', 'Rosette', 'XPO:0102386', 'abnormal electrically active cell morphology', 0.6428571428571429, 5.43643956286526, 1.869452862390249, 'HP:0025461', 'Abnormal cell morphology'),
(464690, 'HP:0031925', 'Rosette', 'XPO:0100817', 'abnormal intersomitic neuron', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(464691, 'HP:0031925', 'Rosette', 'XPO:0102307', 'abnormal dorsal vegetal hemisphere blastomere morphology', 0.46153846153846156, 5.43643956286526, 1.5840220806831131, 'HP:0025461', 'Abnormal cell morphology'),
(464692, 'HP:0031925', 'Rosette', 'XPO:0129421', 'decreased size of the cementoblast', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(464693, 'HP:0031925', 'Rosette', 'XPO:0128744', 'decreased size of the nucleate erythrocyte', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(464694, 'HP:0031925', 'Rosette', 'XPO:0131031', 'abnormally increased number of nucleate erythrocyte', 0.42424242424242425, 3.6715585125471644, 1.2480508339450433, 'UPHENO:0086172', 'abnormal cell'),
(464695, 'HP:0031925', 'Rosette', 'XPO:0101297', 'abnormal barrier cell', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(464696, 'HP:0031925', 'Rosette', 'XPO:0103644', 'abnormally decreased number of cilium in the multiciliated cell', 0.4117647058823529, 3.6715585125471644, 1.229560169755361, 'UPHENO:0086172', 'abnormal cell'),
(464697, 'HP:0031925', 'Rosette', 'XPO:0130231', 'increased size of the melanoblast', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(464698, 'HP:0031925', 'Rosette', 'XPO:0100337', 'abnormal zygote', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(464699, 'HP:0031925', 'Rosette', 'XPO:0103112', 'abnormal stage V oocyte morphology', 0.5625, 5.43643956286526, 1.748713027947041, 'HP:0025461', 'Abnormal cell morphology'),
(464700, 'HP:0031925', 'Rosette', 'XPO:0100372', 'abnormal hematological system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(464701, 'HP:0031925', 'Rosette', 'XPO:0127217', 'abnormally localised cilium', 0.42424242424242425, 3.6715585125471644, 1.2480508339450433, 'UPHENO:0086172', 'abnormal cell'),
(464702, 'HP:0031925', 'Rosette', 'XPO:0141026', 'abnormally necrotic ligament cell', 0.43902439024390244, 5.43643956286526, 1.5449043867452603, 'HP:0025461', 'Abnormal cell morphology'),
(464703, 'HP:0031925', 'Rosette', 'XPO:0101547', 'abnormal lampbrush chromosome', 0.52, 3.6715585125471644, 1.3817418089225373, 'UPHENO:0086172', 'abnormal cell'),
(464704, 'HP:0031925', 'Rosette', 'XPO:0129636', 'increased size of the chondroblast', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(464705, 'HP:0031925', 'Rosette', 'XPO:0140944', 'abnormally necrotic blastomere V1', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(464706, 'HP:0031925', 'Rosette', 'XPO:0102601', 'abnormal disaggregated/reaggregated ectoderm treated with activin morphology', 0.48, 2.7446671847279203, 1.1477979999413668, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(464707, 'HP:0031925', 'Rosette', 'XPO:0100397', 'abnormal ventral vegetal hemisphere blastomere', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(464708, 'HP:0031925', 'Rosette', 'XPO:0129438', 'decreased size of the mitotic cell', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(464709, 'HP:0031925', 'Rosette', 'XPO:0102745', 'abnormal stage IV oocyte morphology', 0.5625, 5.43643956286526, 1.748713027947041, 'HP:0025461', 'Abnormal cell morphology'),
(464710, 'HP:0031925', 'Rosette', 'XPO:0140868', 'abnormally necrotic chondroblast', 0.5625, 5.43643956286526, 1.748713027947041, 'HP:0025461', 'Abnormal cell morphology'),
(464711, 'HP:0031925', 'Rosette', 'XPO:0101976', 'abnormal portion of organism substance morphology', 0.5217391304347826, 2.7446671847279203, 1.196662137068282, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(464712, 'HP:0031925', 'Rosette', 'XPO:0133449', 'decreased size of the cilium in the multiciliated cell', 0.41025641025641024, 3.6715585125471644, 1.2273061620492112, 'UPHENO:0086172', 'abnormal cell'),
(464713, 'HP:0031925', 'Rosette', 'XPO:0102004', 'abnormal hematological system morphology', 0.42424242424242425, 2.7446671847279203, 1.0790756508176813, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(464714, 'HP:0031925', 'Rosette', 'XPO:0131383', 'abnormally decreased number of cementoblast', 0.4117647058823529, 3.6715585125471644, 1.229560169755361, 'UPHENO:0086172', 'abnormal cell'),
(464715, 'HP:0031925', 'Rosette', 'XPO:0129223', 'decreased size of the centriole', 0.4444444444444444, 3.6715585125471644, 1.2774207542365574, 'UPHENO:0086172', 'abnormal cell'),
(464716, 'HP:0031925', 'Rosette', 'XPO:0131599', 'decreased size of the actin filament', 0.4444444444444444, 3.6715585125471644, 1.2774207542365574, 'UPHENO:0086172', 'abnormal cell'),
(464717, 'HP:0031925', 'Rosette', 'XPO:0131134', 'abnormally increased number of barrier cell', 0.42424242424242425, 3.6715585125471644, 1.2480508339450433, 'UPHENO:0086172', 'abnormal cell'),
(464718, 'HP:0031925', 'Rosette', 'XPO:0107354', 'abnormal ventral side morphology', 0.41379310344827586, 2.7446671847279203, 1.0657036887902793, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(464719, 'HP:0031925', 'Rosette', 'XPO:0125715', 'absent barrier cell', 0.42424242424242425, 3.6715585125471644, 1.2480508339450433, 'UPHENO:0086172', 'abnormal cell'),
(464720, 'HP:0031925', 'Rosette', 'XPO:0102943', 'abnormal bottle cell morphology', 0.5294117647058824, 5.43643956286526, 1.696500828969256, 'HP:0025461', 'Abnormal cell morphology'),
(464721, 'HP:0031925', 'Rosette', 'XPO:0129006', 'decreased size of the myelin accumulating cell', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(464722, 'HP:0031925', 'Rosette', 'XPO:0101828', 'abnormal neuron morphology', 0.5142857142857142, 5.43643956286526, 1.6720894724144628, 'HP:0025461', 'Abnormal cell morphology'),
(464723, 'HP:0031925', 'Rosette', 'XPO:0101107', 'abnormal erythroid cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(464724, 'HP:0031925', 'Rosette', 'XPO:0103132', 'abnormal endodermal cell morphology', 0.47368421052631576, 5.43643956286526, 1.6047291305419304, 'HP:0025461', 'Abnormal cell morphology'),
(464725, 'HP:0031925', 'Rosette', 'XPO:0128642', 'decreased size of the centrosome', 0.45714285714285713, 3.6715585125471644, 1.2955411026258445, 'UPHENO:0086172', 'abnormal cell'),
(464726, 'HP:0031925', 'Rosette', 'XPO:0140451', 'abnormally necrotic sensory epithelial cell', 0.47368421052631576, 5.43643956286526, 1.6047291305419304, 'HP:0025461', 'Abnormal cell morphology'),
(464727, 'HP:0031925', 'Rosette', 'XPO:0140580', 'abnormally necrotic migrating myoblast', 0.5142857142857142, 5.43643956286526, 1.6720894724144628, 'HP:0025461', 'Abnormal cell morphology'),
(464728, 'HP:0031925', 'Rosette', 'XPO:0130699', 'increased size of the centriole', 0.4444444444444444, 3.6715585125471644, 1.2774207542365574, 'UPHENO:0086172', 'abnormal cell'),
(464729, 'HP:0031925', 'Rosette', 'XPO:0103179', 'abnormal lampbrush chromosome morphology', 0.5517241379310345, 3.6715585125471644, 1.423266473714053, 'UPHENO:0086172', 'abnormal cell'),
(464730, 'HP:0031925', 'Rosette', 'XPO:0100449', 'abnormal lymphocyte', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(464731, 'HP:0031925', 'Rosette', 'XPO:0102539', 'abnormal cytoplasm morphology', 0.5517241379310345, 3.6715585125471644, 1.423266473714053, 'UPHENO:0086172', 'abnormal cell'),
(464732, 'HP:0031925', 'Rosette', 'XPO:0124864', 'absent germ cell', 0.42424242424242425, 3.6715585125471644, 1.2480508339450433, 'UPHENO:0086172', 'abnormal cell'),
(464733, 'HP:0031925', 'Rosette', 'XPO:0128399', 'decreased size of the pericyte', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(464734, 'HP:0031925', 'Rosette', 'XPO:0129456', 'decreased size of the yolk platelet', 0.43243243243243246, 3.6715585125471644, 1.2600400701560144, 'UPHENO:0086172', 'abnormal cell'),
(464735, 'HP:0031925', 'Rosette', 'XPO:0103113', 'abnormal skeletal muscle satellite cell morphology', 0.43902439024390244, 5.43643956286526, 1.5449043867452603, 'HP:0025461', 'Abnormal cell morphology'),
(464736, 'HP:0031925', 'Rosette', 'XPO:0130895', 'increased size of the cementoblast', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(464737, 'HP:0031925', 'Rosette', 'XPO:0140052', 'abnormally necrotic organ part', 0.42857142857142855, 2.7446671847279203, 1.0845671654222093, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(464738, 'HP:0031925', 'Rosette', 'XPO:0101638', 'abnormal anatomical structure morphology', 0.5217391304347826, 2.7446671847279203, 1.196662137068282, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(464739, 'HP:0031925', 'Rosette', 'XPO:0126983', 'abnormally localised primordial germ cell', 0.42424242424242425, 3.6715585125471644, 1.2480508339450433, 'UPHENO:0086172', 'abnormal cell'),
(464740, 'HP:0031925', 'Rosette', 'XPO:0131308', 'abnormally decreased number of oxygen accumulating cell', 0.4117647058823529, 3.6715585125471644, 1.229560169755361, 'UPHENO:0086172', 'abnormal cell'),
(464741, 'HP:0031925', 'Rosette', 'XPO:0140647', 'abnormally necrotic nucleate erythrocyte', 0.5625, 5.43643956286526, 1.748713027947041, 'HP:0025461', 'Abnormal cell morphology'),
(464742, 'HP:0031925', 'Rosette', 'XPO:0100721', 'abnormal centromere', 0.52, 3.6715585125471644, 1.3817418089225373, 'UPHENO:0086172', 'abnormal cell'),
(464743, 'HP:0031925', 'Rosette', 'XPO:0101835', 'abnormal endocrine cell morphology', 0.5142857142857142, 5.43643956286526, 1.6720894724144628, 'HP:0025461', 'Abnormal cell morphology'),
(464744, 'HP:0031925', 'Rosette', 'XPO:0102255', 'abnormal olfactory sensory neuron morphology', 0.4090909090909091, 5.43643956286526, 1.491307481034791, 'HP:0025461', 'Abnormal cell morphology'),
(464745, 'HP:0031925', 'Rosette', 'XPO:0130989', 'abnormally increased number of ciliated cell', 0.42424242424242425, 3.6715585125471644, 1.2480508339450433, 'UPHENO:0086172', 'abnormal cell'),
(464746, 'HP:0031925', 'Rosette', 'XPO:0131130', 'abnormally increased number of myelin accumulating cell', 0.42424242424242425, 3.6715585125471644, 1.2480508339450433, 'UPHENO:0086172', 'abnormal cell'),
(464747, 'HP:0031925', 'Rosette', 'XPO:0130074', 'increased size of the ciliated cell', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(464748, 'HP:0031925', 'Rosette', 'XPO:0102047', 'abnormal secretory epithelial cell morphology', 0.5454545454545454, 5.43643956286526, 1.7220135512398786, 'HP:0025461', 'Abnormal cell morphology'),
(464749, 'HP:0031925', 'Rosette', 'XPO:0102901', 'abnormal mesodermal cell morphology', 0.47368421052631576, 5.43643956286526, 1.6047291305419304, 'HP:0025461', 'Abnormal cell morphology'),
(464750, 'HP:0031925', 'Rosette', 'XPO:0127743', 'abnormally localised perivitelline space', 0.42424242424242425, 3.6715585125471644, 1.2480508339450433, 'UPHENO:0086172', 'abnormal cell'),
(464751, 'HP:0031925', 'Rosette', 'XPO:0130037', 'increased size of the secondary oogonium', 0.4186046511627907, 5.43643956286526, 1.5085486027240909, 'HP:0025461', 'Abnormal cell morphology'),
(464752, 'HP:0031925', 'Rosette', 'XPO:0139718', 'abnormally necrotic anatomical structure', 0.48, 2.7446671847279203, 1.1477979999413668, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(464753, 'HP:0031925', 'Rosette', 'XPO:0115491', 'abnormally increased distribution of connective tissue', 0.4117647058823529, 2.7446671847279203, 1.0630884610720022, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(464754, 'HP:0031925', 'Rosette', 'XPO:0140284', 'abnormally necrotic dorsal region', 0.41379310344827586, 2.7446671847279203, 1.0657036887902793, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(464755, 'HP:0031925', 'Rosette', 'XPO:0102532', 'abnormal angioblast morphology', 0.5, 5.43643956286526, 1.6487024538808177, 'HP:0025461', 'Abnormal cell morphology'),
(464756, 'HP:0031925', 'Rosette', 'XPO:0131202', 'abnormally decreased number of germ cell', 0.4117647058823529, 3.6715585125471644, 1.229560169755361, 'UPHENO:0086172', 'abnormal cell'),
(464757, 'HP:0031925', 'Rosette', 'XPO:0100396', 'abnormal dorsal animal hemisphere blastomere', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(464758, 'HP:0031925', 'Rosette', 'XPO:0102471', 'abnormal skeletal myocyte morphology', 0.4186046511627907, 5.43643956286526, 1.5085486027240909, 'HP:0025461', 'Abnormal cell morphology'),
(464759, 'HP:0031925', 'Rosette', 'XPO:0140179', 'abnormally necrotic postero-dorsal region', 0.42857142857142855, 2.7446671847279203, 1.0845671654222093, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(464760, 'HP:0031925', 'Rosette', 'XPO:0125997', 'absent Merkel cell', 0.42424242424242425, 3.6715585125471644, 1.2480508339450433, 'UPHENO:0086172', 'abnormal cell'),
(464761, 'HP:0031925', 'Rosette', 'XPO:0128102', 'decreased size of the portion of organism substance', 0.4444444444444444, 2.7446671847279203, 1.104469140402437, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(464762, 'HP:0031925', 'Rosette', 'XPO:0100232', 'abnormal lymphatic system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(464763, 'HP:0031925', 'Rosette', 'XPO:0140059', 'abnormally necrotic epithelial cell', 0.5142857142857142, 5.43643956286526, 1.6720894724144628, 'HP:0025461', 'Abnormal cell morphology'),
(464764, 'HP:0031925', 'Rosette', 'XPO:0103145', 'abnormal basal body morphology', 0.5517241379310345, 3.6715585125471644, 1.423266473714053, 'UPHENO:0086172', 'abnormal cell'),
(464765, 'HP:0031925', 'Rosette', 'XPO:0103130', 'abnormal stage II oocyte morphology', 0.5625, 5.43643956286526, 1.748713027947041, 'HP:0025461', 'Abnormal cell morphology'),
(464766, 'HP:0031925', 'Rosette', 'XPO:0131352', 'abnormally decreased number of barrier cell', 0.4117647058823529, 3.6715585125471644, 1.229560169755361, 'UPHENO:0086172', 'abnormal cell'),
(464767, 'HP:0031925', 'Rosette', 'XPO:0102711', 'abnormal blastomere D1.1.2 morphology', 0.43902439024390244, 5.43643956286526, 1.5449043867452603, 'HP:0025461', 'Abnormal cell morphology'),
(464768, 'HP:0031925', 'Rosette', 'XPO:0127435', 'abnormally localised mitotic spindle', 0.4375, 3.6715585125471644, 1.2674016132384338, 'UPHENO:0086172', 'abnormal cell'),
(464769, 'HP:0031925', 'Rosette', 'XPO:0131645', 'increased size of the cortical actin cytoskeleton', 0.4444444444444444, 3.6715585125471644, 1.2774207542365574, 'UPHENO:0086172', 'abnormal cell'),
(464770, 'HP:0031925', 'Rosette', 'XPO:0101072', 'abnormal mitochondrial cloud', 0.48148148148148145, 3.6715585125471644, 1.3295816755533123, 'UPHENO:0086172', 'abnormal cell'),
(464771, 'HP:0031925', 'Rosette', 'XPO:0102514', 'abnormal perichondrial cell morphology', 0.46153846153846156, 5.43643956286526, 1.5840220806831131, 'HP:0025461', 'Abnormal cell morphology'),
(464772, 'HP:0031925', 'Rosette', 'XPO:0126133', 'absent mitotic cell', 0.42424242424242425, 3.6715585125471644, 1.2480508339450433, 'UPHENO:0086172', 'abnormal cell'),
(464773, 'HP:0031925', 'Rosette', 'XPO:0127740', 'abnormally localised yolk platelet', 0.4117647058823529, 3.6715585125471644, 1.229560169755361, 'UPHENO:0086172', 'abnormal cell'),
(464774, 'HP:0031925', 'Rosette', 'XPO:0102449', 'abnormal intersomitic neuron morphology', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(464775, 'HP:0031925', 'Rosette', 'XPO:0140708', 'abnormally necrotic hatching gland cell', 0.4090909090909091, 5.43643956286526, 1.491307481034791, 'HP:0025461', 'Abnormal cell morphology'),
(464776, 'HP:0031925', 'Rosette', 'XPO:0130116', 'increased size of the secondary spermatogonium', 0.4186046511627907, 5.43643956286526, 1.5085486027240909, 'HP:0025461', 'Abnormal cell morphology'),
(464777, 'HP:0031925', 'Rosette', 'XPO:0101133', 'abnormal motor neuron', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(464778, 'HP:0031925', 'Rosette', 'XPO:0102258', 'abnormal primordial germ cell morphology', 0.6, 5.43643956286526, 1.8060630492092893, 'HP:0025461', 'Abnormal cell morphology'),
(464779, 'HP:0031925', 'Rosette', 'XPO:0125868', 'absent cementoblast', 0.42424242424242425, 3.6715585125471644, 1.2480508339450433, 'UPHENO:0086172', 'abnormal cell'),
(464780, 'HP:0031925', 'Rosette', 'XPO:0128502', 'decreased size of the anatomical line', 0.4444444444444444, 2.7446671847279203, 1.104469140402437, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(464781, 'HP:0031925', 'Rosette', 'XPO:0142043', 'decreased size of the desmosome', 0.45714285714285713, 3.6715585125471644, 1.2955411026258445, 'UPHENO:0086172', 'abnormal cell'),
(464782, 'HP:0031925', 'Rosette', 'XPO:0133445', 'abnormally increased number of cilium in the ciliated non-epidermal cell', 0.42424242424242425, 3.6715585125471644, 1.2480508339450433, 'UPHENO:0086172', 'abnormal cell'),
(464783, 'HP:0031925', 'Rosette', 'XPO:0140450', 'abnormally necrotic mesenchymal stem cell', 0.5142857142857142, 5.43643956286526, 1.6720894724144628, 'HP:0025461', 'Abnormal cell morphology'),
(464784, 'HP:0031925', 'Rosette', 'XPO:0131512', 'absent adherens junction', 0.42424242424242425, 3.6715585125471644, 1.2480508339450433, 'UPHENO:0086172', 'abnormal cell'),
(464785, 'HP:0031925', 'Rosette', 'XPO:0101821', 'abnormal enteroendocrine cell morphology', 0.4864864864864865, 5.43643956286526, 1.626270082715184, 'HP:0025461', 'Abnormal cell morphology'),
(464786, 'HP:0031925', 'Rosette', 'XPO:0125061', 'absent basal body', 0.42424242424242425, 3.6715585125471644, 1.2480508339450433, 'UPHENO:0086172', 'abnormal cell'),
(464787, 'HP:0031925', 'Rosette', 'XPO:0100993', 'abnormal ligament cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(464788, 'HP:0031925', 'Rosette', 'XPO:0127486', 'abnormally localised kinetochore', 0.4375, 3.6715585125471644, 1.2674016132384338, 'UPHENO:0086172', 'abnormal cell'),
(464789, 'HP:0031925', 'Rosette', 'XPO:0101141', 'abnormal Keller explant', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(464790, 'HP:0031925', 'Rosette', 'XPO:0102484', 'abnormal interdigital region morphology', 0.42424242424242425, 2.7446671847279203, 1.0790756508176813, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(464791, 'HP:0031925', 'Rosette', 'XPO:0126318', 'abnormally localised cell', 0.4827586206896552, 3.6715585125471644, 1.3313438786799716, 'UPHENO:0086172', 'abnormal cell'),
(464792, 'HP:0031925', 'Rosette', 'XPO:0129081', 'decreased size of the multiciliated cell precursor', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(464793, 'HP:0031925', 'Rosette', 'XPO:0102742', 'abnormal cell-free extract morphology', 0.48, 2.7446671847279203, 1.1477979999413668, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(464794, 'HP:0031925', 'Rosette', 'XPO:0102636', 'abnormal acid secreting cell morphology', 0.6428571428571429, 5.43643956286526, 1.869452862390249, 'HP:0025461', 'Abnormal cell morphology'),
(464795, 'HP:0031925', 'Rosette', 'XPO:0102982', 'abnormal blastomere D2.1.2 morphology', 0.43902439024390244, 5.43643956286526, 1.5449043867452603, 'HP:0025461', 'Abnormal cell morphology'),
(464796, 'HP:0031925', 'Rosette', 'XPO:0140622', 'abnormally necrotic migrating neuroblast', 0.46153846153846156, 5.43643956286526, 1.5840220806831131, 'HP:0025461', 'Abnormal cell morphology'),
(464797, 'HP:0031925', 'Rosette', 'XPO:0131569', 'abnormally localised cortical actin cytoskeleton', 0.42424242424242425, 3.6715585125471644, 1.2480508339450433, 'UPHENO:0086172', 'abnormal cell'),
(464798, 'HP:0031925', 'Rosette', 'XPO:0100976', 'abnormal multiciliated cell', 0.52, 3.6715585125471644, 1.3817418089225373, 'UPHENO:0086172', 'abnormal cell'),
(464799, 'HP:0031925', 'Rosette', 'XPO:0126413', 'abnormally localised cell part', 0.4666666666666667, 3.6715585125471644, 1.308966757607698, 'UPHENO:0086172', 'abnormal cell'),
(464800, 'HP:0031925', 'Rosette', 'XPO:0140470', 'abnormally necrotic blastomere D2', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(464801, 'HP:0031925', 'Rosette', 'XPO:0100802', 'abnormal exocrine cell', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(464802, 'HP:0031925', 'Rosette', 'XPO:0102029', 'abnormal ventral vegetal hemisphere blastomere morphology', 0.46153846153846156, 5.43643956286526, 1.5840220806831131, 'HP:0025461', 'Abnormal cell morphology'),
(464803, 'HP:0031925', 'Rosette', 'XPO:0102345', 'abnormal monociliated cell morphology', 0.4090909090909091, 5.43643956286526, 1.491307481034791, 'HP:0025461', 'Abnormal cell morphology'),
(464804, 'HP:0031925', 'Rosette', 'XPO:0101909', 'abnormal blastocoel morphology', 0.42857142857142855, 2.7446671847279203, 1.0845671654222093, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(464805, 'HP:0031925', 'Rosette', 'XPO:0141147', 'abnormally necrotic alkali secreting cell', 0.5625, 5.43643956286526, 1.748713027947041, 'HP:0025461', 'Abnormal cell morphology'),
(464806, 'HP:0031925', 'Rosette', 'XPO:0126472', 'abnormally localised secondary spermatogonium', 0.42424242424242425, 3.6715585125471644, 1.2480508339450433, 'UPHENO:0086172', 'abnormal cell'),
(464807, 'HP:0031925', 'Rosette', 'XPO:0103201', 'abnormal activin-induced ectoderm morphology', 0.48, 2.7446671847279203, 1.1477979999413668, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(464808, 'HP:0031925', 'Rosette', 'XPO:0133443', 'abnormally increased number of cilium in the multiciliated cell', 0.42424242424242425, 3.6715585125471644, 1.2480508339450433, 'UPHENO:0086172', 'abnormal cell'),
(464809, 'HP:0031925', 'Rosette', 'XPO:0103146', 'abnormal dendrite morphology', 0.41025641025641024, 3.6715585125471644, 1.2273061620492112, 'UPHENO:0086172', 'abnormal cell'),
(464810, 'HP:0031925', 'Rosette', 'XPO:0127196', 'abnormally localised electrically active cell', 0.45161290322580644, 3.6715585125471644, 1.2876813267322194, 'UPHENO:0086172', 'abnormal cell'),
(464811, 'HP:0031925', 'Rosette', 'XPO:0101472', 'abnormal zygote cortex', 0.5, 3.6715585125471644, 1.3549093166236559, 'UPHENO:0086172', 'abnormal cell'),
(464812, 'HP:0031925', 'Rosette', 'XPO:0102165', 'abnormal melanoblast morphology', 0.6428571428571429, 5.43643956286526, 1.869452862390249, 'HP:0025461', 'Abnormal cell morphology'),
(464813, 'HP:0031925', 'Rosette', 'XPO:0133441', 'abnormally increased number of cilium in the ciliated cell', 0.45161290322580644, 3.6715585125471644, 1.2876813267322194, 'UPHENO:0086172', 'abnormal cell'),
(464814, 'HP:0031925', 'Rosette', 'XPO:0140429', 'abnormally necrotic hemangioblast', 0.47368421052631576, 5.43643956286526, 1.6047291305419304, 'HP:0025461', 'Abnormal cell morphology'),
(464815, 'HP:0031925', 'Rosette', 'XPO:0139763', 'abnormally necrotic anatomical group', 0.41379310344827586, 2.7446671847279203, 1.0657036887902793, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(464816, 'HP:0031925', 'Rosette', 'XPO:0125053', 'absent zygote', 0.42424242424242425, 3.6715585125471644, 1.2480508339450433, 'UPHENO:0086172', 'abnormal cell'),
(464817, 'HP:0031925', 'Rosette', 'XPO:0128859', 'decreased size of the nucleus', 0.45714285714285713, 3.6715585125471644, 1.2955411026258445, 'UPHENO:0086172', 'abnormal cell'),
(464818, 'HP:0031925', 'Rosette', 'XPO:0107357', 'abnormal proximal-distal axis morphology', 0.4444444444444444, 2.7446671847279203, 1.104469140402437, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(464819, 'HP:0031925', 'Rosette', 'XPO:0140697', 'abnormally necrotic digestive enzyme secreting cell', 0.4186046511627907, 5.43643956286526, 1.5085486027240909, 'HP:0025461', 'Abnormal cell morphology'),
(464820, 'HP:0031925', 'Rosette', 'XPO:0125824', 'absent nucleus', 0.42424242424242425, 3.6715585125471644, 1.2480508339450433, 'UPHENO:0086172', 'abnormal cell'),
(464821, 'HP:0031925', 'Rosette', 'XPO:0139886', 'abnormally necrotic process', 0.41379310344827586, 2.7446671847279203, 1.0657036887902793, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(464822, 'HP:0031925', 'Rosette', 'XPO:0140956', 'abnormally necrotic left-dorsal blastomere', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(464823, 'HP:0031925', 'Rosette', 'XPO:0102030', 'abnormal vegetal blastomere morphology', 0.4864864864864865, 5.43643956286526, 1.626270082715184, 'HP:0025461', 'Abnormal cell morphology'),
(464824, 'HP:0031925', 'Rosette', 'XPO:0101834', 'abnormal embryo morphology', 0.42857142857142855, 2.7446671847279203, 1.0845671654222093, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(464825, 'HP:0031925', 'Rosette', 'XPO:0128753', 'decreased size of the melanoblast', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(464826, 'HP:0031925', 'Rosette', 'XPO:0141314', 'abnormal Roux spot morphology', 0.5161290322580645, 3.6715585125471644, 1.376589242279565, 'UPHENO:0086172', 'abnormal cell'),
(464827, 'HP:0031925', 'Rosette', 'XPO:0128737', 'decreased size of the perivitelline space', 0.43243243243243246, 3.6715585125471644, 1.2600400701560144, 'UPHENO:0086172', 'abnormal cell'),
(464828, 'HP:0031925', 'Rosette', 'XPO:0102365', 'abnormal fibroblast morphology', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(464829, 'HP:0031925', 'Rosette', 'XPO:0131553', 'abnormally localised Roux spot', 0.4117647058823529, 3.6715585125471644, 1.229560169755361, 'UPHENO:0086172', 'abnormal cell'),
(464830, 'HP:0031925', 'Rosette', 'XPO:0107412', 'abnormal adult thrombocyte morphology', 0.4090909090909091, 5.43643956286526, 1.491307481034791, 'HP:0025461', 'Abnormal cell morphology'),
(464831, 'HP:0031925', 'Rosette', 'XPO:0130907', 'increased size of the mucus secreting cell', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(464832, 'HP:0031925', 'Rosette', 'XPO:0103223', 'abnormal xanthophore morphology', 0.4186046511627907, 5.43643956286526, 1.5085486027240909, 'HP:0025461', 'Abnormal cell morphology'),
(464833, 'HP:0031925', 'Rosette', 'XPO:0127975', 'abnormally localised mitochondrial cloud', 0.4117647058823529, 3.6715585125471644, 1.229560169755361, 'UPHENO:0086172', 'abnormal cell'),
(464834, 'HP:0031925', 'Rosette', 'XPO:0129571', 'increased size of the anatomical region', 0.41379310344827586, 2.7446671847279203, 1.0657036887902793, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(464835, 'HP:0031925', 'Rosette', 'XPO:0140589', 'abnormally necrotic keratin accumulating cell', 0.5625, 5.43643956286526, 1.748713027947041, 'HP:0025461', 'Abnormal cell morphology'),
(464836, 'HP:0031925', 'Rosette', 'XPO:0141034', 'abnormally necrotic efferent neuron', 0.4186046511627907, 5.43643956286526, 1.5085486027240909, 'HP:0025461', 'Abnormal cell morphology'),
(464837, 'HP:0031925', 'Rosette', 'XPO:0130314', 'increased size of the acid secreting cell', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(464838, 'HP:0031925', 'Rosette', 'XPO:0125559', 'absent electrically active cell', 0.42424242424242425, 3.6715585125471644, 1.2480508339450433, 'UPHENO:0086172', 'abnormal cell'),
(464839, 'HP:0031925', 'Rosette', 'XPO:0129487', 'increased size of the anatomical structure', 0.4444444444444444, 2.7446671847279203, 1.104469140402437, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(464840, 'HP:0031925', 'Rosette', 'XPO:0140373', 'abnormally necrotic whole organism', 0.42857142857142855, 2.7446671847279203, 1.0845671654222093, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(464841, 'HP:0031925', 'Rosette', 'XPO:0142030', 'abnormally localised desmosome', 0.4375, 3.6715585125471644, 1.2674016132384338, 'UPHENO:0086172', 'abnormal cell'),
(464842, 'HP:0031925', 'Rosette', 'XPO:0102285', 'abnormal myoblast morphology', 0.6428571428571429, 5.43643956286526, 1.869452862390249, 'HP:0025461', 'Abnormal cell morphology'),
(464843, 'HP:0031925', 'Rosette', 'XPO:0126697', 'abnormally localised proepicardium', 0.42424242424242425, 3.6715585125471644, 1.2480508339450433, 'UPHENO:0086172', 'abnormal cell'),
(464844, 'HP:0031925', 'Rosette', 'XPO:0140533', 'abnormally necrotic myelin accumulating cell', 0.5625, 5.43643956286526, 1.748713027947041, 'HP:0025461', 'Abnormal cell morphology'),
(464845, 'HP:0031925', 'Rosette', 'XPO:0101968', 'abnormal interneuron morphology', 0.47368421052631576, 5.43643956286526, 1.6047291305419304, 'HP:0025461', 'Abnormal cell morphology'),
(464846, 'HP:0031925', 'Rosette', 'XPO:0130834', 'increased size of the vegetal cortex', 0.42105263157894735, 3.6715585125471644, 1.2433500608051093, 'UPHENO:0086172', 'abnormal cell'),
(464847, 'HP:0031925', 'Rosette', 'XPO:0140955', 'abnormally necrotic ventro-lateral region', 0.42857142857142855, 2.7446671847279203, 1.0845671654222093, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(464848, 'HP:0031925', 'Rosette', 'XPO:0131559', 'abnormally localised spindle microtubule', 0.4117647058823529, 3.6715585125471644, 1.229560169755361, 'UPHENO:0086172', 'abnormal cell'),
(464849, 'HP:0031925', 'Rosette', 'XPO:0102808', 'abnormal non-ciliated epithelial cell morphology', 0.5454545454545454, 5.43643956286526, 1.7220135512398786, 'HP:0025461', 'Abnormal cell morphology'),
