(135070, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0101917', 'abnormal progenitor cell morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(135071, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100642', 'abnormal gustatory system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(135072, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0131328', 'abnormally decreased number of paracrine cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(135073, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100733', 'abnormal fibroblast', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(135074, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0136478', 'increased cell population proliferation in thoracic region', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(135075, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100060', 'abnormal regenerating tissue', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135076, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100397', 'abnormal ventral vegetal hemisphere blastomere', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(135077, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100956', 'abnormal centrosome', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(135078, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100417', 'abnormal dense regular connective tissue', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(135079, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0141797', 'abnormal hydrogen metabolic process', 0.4782608695652174, 4.758907843651163, 1.508641575552437, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(135080, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0141314', 'abnormal Roux spot morphology', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(135081, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0102958', 'abnormal cementoblast morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(135082, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100511', 'abnormal stylopod', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(135083, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0102520', 'abnormal microtubule morphology', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(135084, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100307', 'abnormal blastomere', 0.5652173913043478, 3.6715585125471644, 1.440565418328227, 'UPHENO:0086172', 'abnormal cell'),
(135085, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0127896', 'abnormally localised ring structure', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(135086, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0131553', 'abnormally localised Roux spot', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(135087, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0131130', 'abnormally increased number of myelin accumulating cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(135088, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0101110', 'abnormal cell-free extract', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135089, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0131292', 'abnormally decreased number of mucus secreting cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(135090, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0127740', 'abnormally localised yolk platelet', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(135091, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0133436', 'abnormal cilium morphology in the multiciliated cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(135092, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0127160', 'abnormally localised acid secreting cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(135093, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100308', 'abnormal early embryonic cell', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(135094, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100917', 'abnormal stage III oocyte', 0.5652173913043478, 3.6715585125471644, 1.440565418328227, 'UPHENO:0086172', 'abnormal cell'),
(135095, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0101411', 'abnormal marginal zone (sensu neural)', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135096, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100547', 'abnormal blastomere V2', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(135097, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0139620', 'decreased cell population proliferation in anterior region', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(135098, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0126982', 'abnormally localised secondary oogonium', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(135099, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0101074', 'abnormal germinal vesicle', 0.52, 3.6715585125471644, 1.3817418089225373, 'UPHENO:0086172', 'abnormal cell'),
(135100, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0107284', 'abnormal migrating myoblast', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(135101, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0101389', 'abnormal wedge region', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(135102, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0141792', 'abnormal small molecule metabolic process', 0.4782608695652174, 4.758907843651163, 1.508641575552437, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(135103, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0125692', 'absent oxygen accumulating cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(135104, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0107265', 'abnormal posterior side', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135105, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100344', 'abnormal portion of organism substance', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135106, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0101022', 'abnormal blastomere V1.2', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(135107, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0103179', 'abnormal lampbrush chromosome morphology', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(135108, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0125577', 'absent cilium', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(135109, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0141795', 'abnormal glycosylation', 0.44, 4.758907843651163, 1.447038165082909, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(135110, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0125785', 'absent mitotic spindle', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(135111, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0141860', 'abnormal malate-aspartate shuttle', 0.4583333333333333, 4.758907843651163, 1.4768771428276568, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(135112, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0101113', 'abnormal stage IV oocyte', 0.5652173913043478, 3.6715585125471644, 1.440565418328227, 'UPHENO:0086172', 'abnormal cell'),
(135113, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0141743', 'abnormal chemical homeostasis within a tissue', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(135114, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0131708', 'abnormal cilium disassembly', 0.5555555555555556, 5.835653092541957, 1.8005636605953823, 'HP:0011017', 'Abnormal cellular physiology'),
(135115, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0131195', 'abnormally decreased number of Merkel cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(135116, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0125115', 'absent paracrine cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(135117, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0101452', 'abnormal blastomere V1.1.1', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(135118, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100023', 'abnormal mesenchyme', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135119, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100861', 'abnormal blastomere D2.2.2', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(135120, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0127806', 'abnormally localised spermatid', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(135121, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0101162', 'abnormal stromal cell', 0.48148148148148145, 3.6715585125471644, 1.3295816755533123, 'UPHENO:0086172', 'abnormal cell'),
(135122, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0135483', 'increased cell population proliferation in organism subdivision', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(135123, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0135478', 'increased cell population proliferation in female organism', 0.4166666666666667, 5.835653092541957, 1.5593338712067029, 'HP:0011017', 'Abnormal cellular physiology'),
(135124, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100251', 'abnormal proteinaceous extracellular matrix', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135125, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0103067', 'abnormal paracrine cell morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(135126, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0141772', 'abnormal water homeostasis', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(135127, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0101166', 'abnormal premigratory neural crest cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(135128, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0131354', 'abnormally decreased number of multiciliated cell precursor', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(135129, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0138844', 'decreased cell population proliferation in extracellular matrix', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(135130, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100025', 'abnormal oocyte', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(135131, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0103414', 'abnormally increased number of vacuole in the spermatozoon', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(135132, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0101515', 'abnormal neuromast mantle cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(135133, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0133443', 'abnormally increased number of cilium in the multiciliated cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(135134, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100713', 'abnormal monociliated cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(135135, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0126783', 'abnormally localised exocrine cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(135136, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100028', 'abnormal anatomical cluster', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135137, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100784', 'abnormal left blastomere', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(135138, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0133473', 'abnormally decreased number of cilium in the ciliated non-epidermal cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(135139, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0107426', 'abnormal yolk platelet morphology', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(135140, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0139423', 'decreased cell population proliferation in multicellular anatomical structure', 0.4166666666666667, 5.835653092541957, 1.5593338712067029, 'HP:0011017', 'Abnormal cellular physiology'),
(135141, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100231', 'abnormal compound organ', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135142, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100192', 'abnormal epithelium', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135143, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100335', 'abnormal commissural interneuron', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(135144, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0101333', 'abnormal barrier epithelial cell', 0.6190476190476191, 3.6715585125471644, 1.5076039119696991, 'UPHENO:0086172', 'abnormal cell'),
(135145, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0107272', 'abnormal axial region', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135146, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0102353', 'abnormal centromere morphology', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(135147, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0141715', 'abnormal septum', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135148, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0126738', 'abnormally localised paracrine cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(135149, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100915', 'abnormal dermal system', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135150, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0141745', 'abnormal creatinine homeostasis', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(135151, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0125779', 'absent endoplasmic reticulum', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(135152, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0102423', 'abnormal multiciliated cell precursor morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(135153, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0135476', 'increased cell population proliferation in anatomical system', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(135154, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0126318', 'abnormally localised cell', 0.48148148148148145, 3.6715585125471644, 1.3295816755533123, 'UPHENO:0086172', 'abnormal cell'),
(135155, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0103080', 'abnormal myelin accumulating cell morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(135156, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0130973', 'abnormally increased number of stem cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(135157, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100014', 'abnormal tissue', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135158, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0138232', 'decreased cell population proliferation in forelimb region', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(135159, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0102183', 'abnormal oocyte cortex morphology', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(135160, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0107303', 'abnormal migratory trunk neural crest cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(135161, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0131666', 'abnormal adherens junction', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(135162, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0126697', 'abnormally localised proepicardium', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(135163, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100610', 'abnormal appendage', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135164, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0131685', 'abnormal cortical actin cytoskeleton', 0.5652173913043478, 3.6715585125471644, 1.440565418328227, 'UPHENO:0086172', 'abnormal cell'),
(135165, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0136521', 'increased cell population proliferation in ventral region', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(135166, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0101636', 'abnormal cell morphology', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(135167, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100864', 'abnormal dorsolateral ascending neuron', 0.48148148148148145, 3.6715585125471644, 1.3295816755533123, 'UPHENO:0086172', 'abnormal cell'),
(135168, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0127343', 'abnormally localised filopodium', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(135169, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0107268', 'abnormal left side', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135170, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0130968', 'abnormally increased number of early embryonic cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(135171, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100762', 'abnormal intersomitic region', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135172, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100653', 'abnormal myoblast', 0.6190476190476191, 3.6715585125471644, 1.5076039119696991, 'UPHENO:0086172', 'abnormal cell'),
(135173, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100965', 'abnormal blastomere V2.2', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(135174, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0126630', 'abnormally localised early embryonic cell', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(135175, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0101448', 'abnormal myelin accumulating cell', 0.6190476190476191, 3.6715585125471644, 1.5076039119696991, 'UPHENO:0086172', 'abnormal cell'),
(135176, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100882', 'abnormal perichondrial cell', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(135177, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0101406', 'abnormal cleavage furrow', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135178, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0139130', 'decreased cell population proliferation in interdigital region', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(135179, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0101269', 'abnormal mesodermal cell', 0.48148148148148145, 3.6715585125471644, 1.3295816755533123, 'UPHENO:0086172', 'abnormal cell'),
(135180, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0101519', 'abnormal hypobranchial placode', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135181, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0131314', 'abnormally decreased number of exocrine cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(135182, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0141892', 'abnormal inositol metabolic process', 0.44, 4.758907843651163, 1.447038165082909, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(135183, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0131677', 'abnormal actin filament', 0.5652173913043478, 3.6715585125471644, 1.440565418328227, 'UPHENO:0086172', 'abnormal cell'),
(135184, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100900', 'abnormal angioblast', 0.52, 3.6715585125471644, 1.3817418089225373, 'UPHENO:0086172', 'abnormal cell'),
(135185, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100070', 'abnormal anatomical system', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135186, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100258', 'abnormal organ part', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135187, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0141296', 'abnormal adherens junction morphology', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(135188, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0141775', 'abnormal nitrogen compound metabolic process', 0.4782608695652174, 4.758907843651163, 1.508641575552437, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(135189, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0141770', 'abnormal urate homeostasis', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(135190, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0125394', 'absent multiciliated cell precursor', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(135191, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0131145', 'abnormally increased number of polar body', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(135192, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0102764', 'abnormal apoptotic cell morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(135193, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0142057', 'abnormal desmosome', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(135194, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0107324', 'abnormal embryonic thrombocyte', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(135195, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100465', 'abnormal skeletal system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(135196, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100265', 'abnormal sensory epithelial cell', 0.52, 3.6715585125471644, 1.3817418089225373, 'UPHENO:0086172', 'abnormal cell'),
(135197, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0101325', 'abnormal blastomere D2.1.1', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(135198, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100186', 'abnormal uveal tract', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135199, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0125523', 'absent acid secreting cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(135200, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0141267', 'abnormal resting posture', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(135201, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100372', 'abnormal hematological system', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(135202, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0115509', 'abnormally semi-viable whole organism', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135203, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0141788', 'abnormal hormone biosynthetic process', 0.4074074074074074, 4.758907843651163, 1.392413123563799, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(135204, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0135482', 'increased cell population proliferation in cell', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(135205, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0139669', 'decreased cell population proliferation in ventro-lateral region', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(135206, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0102285', 'abnormal myoblast morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(135207, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0131551', 'abnormally localised actin cytoskeleton', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(135208, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0139625', 'decreased cell population proliferation in antero-dorsal region', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(135209, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100164', 'abnormal neural nucleus', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(135210, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0135509', 'increased cell population proliferation in embryonic structure', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(135211, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100557', 'abnormal prime meridian', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135212, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0101534', 'abnormal blastomere V2.1.1', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(135213, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100675', 'abnormal dorsal vegetal hemisphere blastomere', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(135214, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100549', 'abnormal mitotic cell', 0.6190476190476191, 3.6715585125471644, 1.5076039119696991, 'UPHENO:0086172', 'abnormal cell'),
(135215, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0103099', 'abnormal alkali secreting cell morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(135216, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0131691', 'abnormal molecular function', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(135217, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0107286', 'abnormal efferent neuron', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(135218, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0101969', 'abnormal zygote morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(135219, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100062', 'abnormal anatomical space', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135220, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0142056', 'abnormal main body axis', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135221, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0139621', 'decreased cell population proliferation in posterior region', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(135222, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100654', 'abnormal blastomere V2.1', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(135223, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0138579', 'decreased cell population proliferation in whole organism', 0.42857142857142855, 5.835653092541957, 1.5814531869511603, 'HP:0011017', 'Abnormal cellular physiology'),
(135224, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0127631', 'abnormally localised centriole', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(135225, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0135636', 'increased cell population proliferation in anatomical region', 0.4166666666666667, 5.835653092541957, 1.5593338712067029, 'HP:0011017', 'Abnormal cellular physiology'),
(135226, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100665', 'abnormal egg jelly', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135227, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100509', 'abnormal germ plasm', 0.5, 3.6715585125471644, 1.3549093166236559, 'UPHENO:0086172', 'abnormal cell'),
(135228, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0101485', 'abnormal descending interneuron', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(135229, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0107287', 'abnormal afferent neuron', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(135230, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100993', 'abnormal ligament cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(135231, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0127363', 'abnormally localised barrier cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(135232, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0141271', 'increased surface breathing', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(135233, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0135477', 'increased cell population proliferation in whole organism', 0.42857142857142855, 5.835653092541957, 1.5814531869511603, 'HP:0011017', 'Abnormal cellular physiology'),
(135234, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0141794', 'abnormal prosthetic group metabolic process', 0.4782608695652174, 4.758907843651163, 1.508641575552437, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(135235, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0131513', 'absent actin cytoskeleton', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(135236, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100842', 'abnormal left-dorsal blastomere', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(135237, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100069', 'abnormal urinary system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(135238, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0131075', 'abnormally increased number of mucus secreting cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(135239, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100104', 'abnormal embryonic structure', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135240, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100239', 'abnormal acellular anatomical structure', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135241, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0101327', 'abnormal blastomere V1.2.1', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(135242, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0127168', 'abnormally localised chondroblast', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(135243, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0142051', 'abnormal cerebrospinal fluid', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(135244, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0136028', 'increased cell population proliferation in interdigital region', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(135245, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0102531', 'abnormal secondary spermatogonium morphology', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(135246, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0107269', 'abnormal right side', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135247, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0138581', 'decreased cell population proliferation in male organism', 0.4166666666666667, 5.835653092541957, 1.5593338712067029, 'HP:0011017', 'Abnormal cellular physiology'),
(135248, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0101264', 'abnormal mitotic spindle', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(135249, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0102703', 'abnormal endoplasmic reticulum morphology', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(135250, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100176', 'abnormal stage VI oocyte', 0.5652173913043478, 3.6715585125471644, 1.440565418328227, 'UPHENO:0086172', 'abnormal cell'),
(135251, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0138837', 'decreased cell population proliferation in process', 0.4166666666666667, 5.835653092541957, 1.5593338712067029, 'HP:0011017', 'Abnormal cellular physiology'),
(135252, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0139717', 'abnormally necrotic cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(135253, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0131687', 'abnormal astral microtubule', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(135254, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0101497', 'abnormal ciliary axoneme', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(135255, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0103636', 'abnormally increased number of melanoblast', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(135256, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0102258', 'abnormal primordial germ cell morphology', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(135257, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0102356', 'abnormal kinetochore morphology', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(135258, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0101740', 'abnormal cell part morphology', 0.48148148148148145, 3.6715585125471644, 1.3295816755533123, 'UPHENO:0086172', 'abnormal cell'),
(135259, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0141498', 'abnormal axon microtubule bundle', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(135260, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0131351', 'abnormally decreased number of apoptotic cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(135261, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0141767', 'abnormal temperature homeostasis', 0.4074074074074074, 4.758907843651163, 1.392413123563799, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(135262, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0141787', 'abnormal hormone metabolic process', 0.4782608695652174, 4.758907843651163, 1.508641575552437, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(135263, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100289', 'abnormal chondroblast', 0.6190476190476191, 3.6715585125471644, 1.5076039119696991, 'UPHENO:0086172', 'abnormal cell'),
(135264, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0107258', 'abnormal anatomical axis', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135265, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0138838', 'decreased cell population proliferation in cell condensation', 0.4166666666666667, 5.835653092541957, 1.5593338712067029, 'HP:0011017', 'Abnormal cellular physiology'),
(135266, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100332', 'abnormal germinal granule', 0.48148148148148145, 3.6715585125471644, 1.3295816755533123, 'UPHENO:0086172', 'abnormal cell'),
(135267, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0102539', 'abnormal cytoplasm morphology', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(135268, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0126737', 'abnormally localised mesenchymal stem cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(135269, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0102336', 'abnormal Merkel cell morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(135270, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0101513', 'abnormal basal body', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(135271, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0124884', 'absent keratin accumulating cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(135272, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0136398', 'increased cell population proliferation in egg jelly', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(135273, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100493', 'abnormal liver and biliary system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(135274, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0141771', 'abnormal urea homeostasis', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(135275, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100196', 'abnormal neuron', 0.5, 3.6715585125471644, 1.3549093166236559, 'UPHENO:0086172', 'abnormal cell'),
(135276, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0131569', 'abnormally localised cortical actin cytoskeleton', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(135277, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0101168', 'abnormal circulating cell', 0.52, 3.6715585125471644, 1.3817418089225373, 'UPHENO:0086172', 'abnormal cell'),
(135278, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0127643', 'abnormally localised somatic stem cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(135279, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100203', 'abnormal endocrine cell', 0.5, 3.6715585125471644, 1.3549093166236559, 'UPHENO:0086172', 'abnormal cell'),
(135280, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100002', 'abnormal head', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(135281, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0101200', 'abnormal joint region', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135282, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0139628', 'decreased cell population proliferation in postero-ventral region', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(135283, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0116494', 'absent biological process', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(135284, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0101023', 'abnormal ultimobranchial body', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(135285, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100398', 'abnormal vegetal blastomere', 0.48148148148148145, 3.6715585125471644, 1.3295816755533123, 'UPHENO:0086172', 'abnormal cell'),
(135286, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0141784', 'abnormal cellular hormone metabolic process', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(135287, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100745', 'abnormal anterior lymph sac', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(135288, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100585', 'abnormal elastica externa', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(135289, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0101283', 'abnormal left-ventral blastomere', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(135290, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100503', 'abnormal blastomere D2', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(135291, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0115391', 'abnormally undifferentiated alimentary system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(135292, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0135788', 'increased cell population proliferation in intersomitic region', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(135293, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0102181', 'abnormal mitotic cell morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(135294, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0127975', 'abnormally localised mitochondrial cloud', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(135295, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100573', 'abnormal extraembryonic structure', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135296, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0124716', 'absent cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(135297, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0127486', 'abnormally localised kinetochore', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(135298, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0101221', 'abnormal larval immune system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(135299, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100277', 'abnormal blastocoel', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135300, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0131348', 'abnormally decreased number of absorptive cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(135301, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0101451', 'abnormal dorsal lymph space', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(135302, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100339', 'abnormal circumblastoporal collar', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135303, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0141841', 'abnormality of whole organism mass', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(135304, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0107266', 'abnormal dorsal side', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135305, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0102852', 'abnormal centriole morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(135306, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0101450', 'abnormal myeloid cell', 0.5, 3.6715585125471644, 1.3549093166236559, 'UPHENO:0086172', 'abnormal cell'),
(135307, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0135742', 'increased cell population proliferation in extracellular matrix', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(135308, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0136321', 'increased cell population proliferation in multicellular anatomical structure', 0.4166666666666667, 5.835653092541957, 1.5593338712067029, 'HP:0011017', 'Abnormal cellular physiology'),
(135309, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0126725', 'abnormally localised epithelial cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(135310, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100084', 'abnormal anatomical group', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135311, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0138717', 'decreased cell population proliferation in acellular anatomical structure', 0.4166666666666667, 5.835653092541957, 1.5593338712067029, 'HP:0011017', 'Abnormal cellular physiology'),
(135312, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0125997', 'absent Merkel cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(135313, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100674', 'abnormal secondary oogonium', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(135314, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100422', 'abnormal notochord', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(135315, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0125824', 'absent nucleus', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(135316, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0131248', 'abnormally decreased number of acid secreting cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(135317, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0133438', 'abnormal cilium morphology in the ciliated non-epidermal cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(135318, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100205', 'abnormal limb segment', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(135319, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0125750', 'absent melanoblast', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(135320, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0138822', 'decreased cell population proliferation in extraembryonic structure', 0.4166666666666667, 5.835653092541957, 1.5593338712067029, 'HP:0011017', 'Abnormal cellular physiology'),
(135321, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0125533', 'absent myelin accumulating cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(135322, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0131707', 'abnormal cilium assembly', 0.5172413793103449, 5.835653092541957, 1.7373661832679608, 'HP:0011017', 'Abnormal cellular physiology'),
(135323, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0101040', 'abnormal axial mesoderm', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135324, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100081', 'abnormal anatomical entity in vitro', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135325, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0139619', 'decreased cell population proliferation in basal region', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(135326, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0107270', 'abnormal proximal-distal axis', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135327, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0127391', 'abnormally localised lampbrush chromosome', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(135328, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0101079', 'abnormal blastomere D1.1.2', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(135329, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100386', 'abnormal limb', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(135330, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0141272', 'absent surface breathing', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(135331, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0101094', 'abnormal blastomere V2.2.1', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(135332, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0131205', 'abnormally decreased number of ciliated cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(135333, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0107399', 'abnormal filopodium morphology', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(135334, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0141778', 'abnormal biosynthetic process', 0.4782608695652174, 4.758907843651163, 1.508641575552437, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(135335, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0102693', 'abnormal plasma membrane morphology', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(135336, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0135322', 'increased cell population proliferation in marginal zone (sensu neural)', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(135337, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0141911', 'abnormal ribose phosphate metabolic process', 0.4230769230769231, 4.758907843651163, 1.418937661667548, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(135338, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0138606', 'decreased cell population proliferation in multi-tissue structure', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(135339, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100006', 'abnormal anatomical structure', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135340, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0136523', 'increased cell population proliferation in antero-dorsal region', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(135341, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0138585', 'decreased cell population proliferation in organism subdivision', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(135342, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0107262', 'abnormal left-right axis', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135343, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100031', 'abnormal central nervous system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(135344, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0141315', 'abnormal anatomical region', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135345, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0138577', 'decreased cell population proliferation in anatomical group', 0.4166666666666667, 5.835653092541957, 1.5593338712067029, 'HP:0011017', 'Abnormal cellular physiology'),
(135346, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100691', 'abnormal keratin accumulating cell', 0.6190476190476191, 3.6715585125471644, 1.5076039119696991, 'UPHENO:0086172', 'abnormal cell'),
(135347, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100991', 'abnormal iliac process primordium', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135348, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0101409', 'abnormal perivitelline space', 0.5652173913043478, 3.6715585125471644, 1.440565418328227, 'UPHENO:0086172', 'abnormal cell'),
(135349, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0130988', 'abnormally increased number of pericyte', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(135350, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0101220', 'abnormal centriole', 0.5652173913043478, 3.6715585125471644, 1.440565418328227, 'UPHENO:0086172', 'abnormal cell'),
(135351, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0126162', 'absent alkali secreting cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(135352, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0127979', 'abnormally localised absorptive cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(135353, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0127653', 'abnormally localised Merkel cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(135354, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100395', 'abnormal blastomere D1.1', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(135355, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0102588', 'abnormal centrosome morphology', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(135356, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0126388', 'abnormally localised oocyte', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(135357, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100114', 'abnormal peripheral nervous system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(135358, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100791', 'abnormal multiciliated cell precursor', 0.6190476190476191, 3.6715585125471644, 1.5076039119696991, 'UPHENO:0086172', 'abnormal cell'),
(135359, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0127428', 'abnormally localised endoplasmic reticulum', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(135360, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100954', 'abnormal neural progenitor cell', 0.48148148148148145, 3.6715585125471644, 1.3295816755533123, 'UPHENO:0086172', 'abnormal cell'),
(135361, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0131308', 'abnormally decreased number of oxygen accumulating cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(135362, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0103894', 'abnormally decreased number of spindle microtubule', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(135363, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0127288', 'abnormally localised pericyte', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(135364, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0125530', 'absent chondroblast', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(135365, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100989', 'abnormal right blastomere', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(135366, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0131667', 'abnormal actin cytoskeleton', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(135367, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100035', 'abnormal ventral animal hemisphere blastomere', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(135368, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0101350', 'abnormal blastomere D2.1.2', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(135369, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0101466', 'abnormal secondary myofiber', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(135370, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0131082', 'abnormally increased number of alkali secreting cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(135371, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0125724', 'absent polar body', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(135372, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100316', 'abnormal gamete', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(135373, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0107271', 'abnormal apical region', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135374, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0127876', 'abnormally localised microtubule', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(135375, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0101504', 'abnormal blastomere D2.2.1', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(135376, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0124845', 'absent stem cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(135377, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0131561', 'abnormally localised actin filament', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(135378, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100225', 'abnormal endocrine system', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(135379, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0127476', 'abnormally localised nucleus', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(135380, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0131725', 'abnormal phosphorylation of RNA polymerase II C-terminal domain', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(135381, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0126473', 'abnormally localised germ cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(135382, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0136522', 'increased cell population proliferation in medial region', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(135383, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100152', 'abnormal alimentary system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(135384, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100458', 'abnormal autopod', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(135385, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0141776', 'abnormal metabolic process', 0.5238095238095238, 4.758907843651163, 1.5788480773767701, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(135386, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100969', 'abnormal disaggregated/reaggregated ectoderm treated with activin', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135387, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0127522', 'abnormally localised cementoblast', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(135388, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100823', 'abnormal blood', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(135389, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0131096', 'abnormally increased number of exocrine cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(135390, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0131061', 'abnormally increased number of keratin accumulating cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(135391, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0127217', 'abnormally localised cilium', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(135392, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0127821', 'abnormally localised apoptotic cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(135393, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0101569', 'abnormal activin-induced ectoderm', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135394, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0101176', 'abnormal non-ciliated epithelial cell', 0.52, 3.6715585125471644, 1.3817418089225373, 'UPHENO:0086172', 'abnormal cell'),
(135395, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0139670', 'decreased cell population proliferation in dorso-lateral region', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(135396, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0107311', 'abnormal apical junction complex', 0.5, 3.6715585125471644, 1.3549093166236559, 'UPHENO:0086172', 'abnormal cell'),
(135397, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100545', 'abnormal male organism', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135398, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100531', 'abnormal proliferative region', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135399, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0131066', 'abnormally increased number of myoblast', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(135400, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0103642', 'increased cell population proliferation', 0.5172413793103449, 5.835653092541957, 1.7373661832679608, 'HP:0011017', 'Abnormal cellular physiology'),
(135401, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0142052', 'abnormal nasal region', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(135402, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0131131', 'abnormally increased number of absorptive cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(135403, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0101570', 'abnormal forelimb region', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135404, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0127815', 'abnormally localised ciliated non-epidermal cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(135405, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0131352', 'abnormally decreased number of barrier cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(135406, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0101212', 'abnormal glomeral mesenchyme', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(135407, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0102534', 'abnormal spermatocyte morphology', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(135408, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100218', 'abnormal epithelial cell', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(135409, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0102434', 'abnormal exocrine cell morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(135410, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0101374', 'abnormal migratory neural crest cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(135411, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0135720', 'increased cell population proliferation in extraembryonic structure', 0.4166666666666667, 5.835653092541957, 1.5593338712067029, 'HP:0011017', 'Abnormal cellular physiology'),
(135412, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0135736', 'increased cell population proliferation in cell condensation', 0.4166666666666667, 5.835653092541957, 1.5593338712067029, 'HP:0011017', 'Abnormal cellular physiology'),
(135413, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0138576', 'decreased cell population proliferation in anatomical structure', 0.4411764705882353, 5.835653092541957, 1.6045413160604438, 'HP:0011017', 'Abnormal cellular physiology'),
(135414, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0133471', 'abnormally decreased number of cilium in the ciliated cell', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(135415, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100232', 'abnormal lymphatic system', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(135416, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0131694', 'abnormal RNA polymerase II activity', 0.4230769230769231, 4.758907843651163, 1.418937661667548, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(135417, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0103021', 'abnormal wedge region morphology', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(135418, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100521', 'abnormal animal blastomere', 0.48148148148148145, 3.6715585125471644, 1.3295816755533123, 'UPHENO:0086172', 'abnormal cell'),
(135419, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0131165', 'abnormally increased number of cementoblast', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(135420, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100899', 'abnormal secondary spermatogonium', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(135421, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0136517', 'increased cell population proliferation in basal region', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(135422, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0135504', 'increased cell population proliferation in multi-tissue structure', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(135423, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0125743', 'absent lampbrush chromosome', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(135424, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0101535', 'abnormal absorptive cell', 0.6190476190476191, 3.6715585125471644, 1.5076039119696991, 'UPHENO:0086172', 'abnormal cell'),
(135425, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0101141', 'abnormal Keller explant', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135426, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0101016', 'abnormal egg', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(135427, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0101311', 'abnormal bottle cell', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(135428, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0101358', 'abnormal endothelial cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(135429, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0131550', 'abnormally localised adherens junction', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(135430, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0141421', 'decreased cell population proliferation in tadpole', 0.4166666666666667, 5.835653092541957, 1.5593338712067029, 'HP:0011017', 'Abnormal cellular physiology'),
(135431, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0141277', 'abnormal actin cytoskeleton morphology', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(135432, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100202', 'abnormal embryo', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135433, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0139580', 'decreased cell population proliferation in thoracic region', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(135434, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0102526', 'abnormal nucleus morphology', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(135435, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0131346', 'abnormally decreased number of chondroblast', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(135436, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0101490', 'abnormal ectodermal cell', 0.48148148148148145, 3.6715585125471644, 1.3295816755533123, 'UPHENO:0086172', 'abnormal cell'),
(135437, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0141904', 'abnormal glucosamine metabolic process', 0.4782608695652174, 4.758907843651163, 1.508641575552437, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(135438, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0102934', 'abnormal subcortical cytoplasm morphology', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(135439, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0135474', 'increased cell population proliferation in anatomical structure', 0.4411764705882353, 5.835653092541957, 1.6045413160604438, 'HP:0011017', 'Abnormal cellular physiology'),
(135440, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0101940', 'abnormal early embryonic cell morphology', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(135441, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0101237', 'abnormal mucus secreting cell', 0.6190476190476191, 3.6715585125471644, 1.5076039119696991, 'UPHENO:0086172', 'abnormal cell'),
(135442, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0126133', 'absent mitotic cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(135443, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0102165', 'abnormal melanoblast morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(135444, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100862', 'abnormal blastomere V1', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(135445, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100363', 'abnormal cardiovascular system', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135446, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0126214', 'absent microtubule', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(135447, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0102896', 'abnormal mitotic spindle morphology', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(135448, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0138584', 'decreased cell population proliferation in cell', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(135449, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100894', 'abnormal nucleus', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(135450, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0142023', 'absent desmosome', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(135451, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0131180', 'abnormally decreased number of cell', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(135452, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0131189', 'abnormally decreased number of stem cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(135453, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0138609', 'decreased cell population proliferation in tissue', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(135454, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0101503', 'abnormal organ cortex', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135455, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0101405', 'abnormal ring structure', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(135456, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0126628', 'abnormally localised blastomere', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(135457, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0101362', 'abnormal vegetal cortex', 0.52, 3.6715585125471644, 1.3817418089225373, 'UPHENO:0086172', 'abnormal cell'),
(135458, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0102869', 'abnormal mucus secreting cell morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(135459, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0141880', 'abnormal ethanolamine metabolic process', 0.4074074074074074, 4.758907843651163, 1.392413123563799, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(135460, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0115615', 'abnormally posteriorly mislocalised primordial germ cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(135461, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100754', 'abnormal electrically active cell', 0.6190476190476191, 3.6715585125471644, 1.5076039119696991, 'UPHENO:0086172', 'abnormal cell'),
(135462, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0141266', 'abnormal surface breathing', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(135463, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0136518', 'increased cell population proliferation in anterior region', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(135464, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0127513', 'abnormally localised nucleate erythrocyte', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(135465, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0141783', 'abnormal collagen metabolic process', 0.4782608695652174, 4.758907843651163, 1.508641575552437, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(135466, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0115758', 'abnormally decreased mobility of melanoblast', 0.52, 3.6715585125471644, 1.3817418089225373, 'UPHENO:0086172', 'abnormal cell'),
(135467, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100032', 'abnormal nervous system', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(135468, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0141898', 'abnormal maltose metabolic process', 0.4230769230769231, 4.758907843651163, 1.418937661667548, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(135469, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0101136', 'abnormal ooplasm', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(135470, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100976', 'abnormal multiciliated cell', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(135471, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0126082', 'absent perivitelline space', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(135472, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100034', 'abnormal blastomere V1.1', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(135473, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100172', 'abnormal stem cell', 0.6190476190476191, 3.6715585125471644, 1.5076039119696991, 'UPHENO:0086172', 'abnormal cell'),
(135474, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0130986', 'abnormally increased number of germ cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(135475, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0101481', 'abnormal skeletal muscle satellite cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(135476, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0141796', 'abnormal demethylation', 0.4782608695652174, 4.758907843651163, 1.508641575552437, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(135477, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100843', 'abnormal fasciculated network of fibrils', 0.5, 3.6715585125471644, 1.3549093166236559, 'UPHENO:0086172', 'abnormal cell'),
(135478, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0102929', 'abnormal barrier cell morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(135479, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0141782', 'abnormal methylation', 0.4782608695652174, 4.758907843651163, 1.508641575552437, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(135480, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0127520', 'abnormally localised gastrula cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(135481, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100273', 'abnormal visual system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(135482, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0131300', 'abnormally decreased number of alkali secreting cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(135483, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0101071', 'abnormal endoplasmic reticulum', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(135484, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0102994', 'abnormal vegetal cortex morphology', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(135485, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0101547', 'abnormal lampbrush chromosome', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(135486, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0131171', 'abnormally increased number of barrier epithelial cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(135487, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0103644', 'abnormally decreased number of cilium in the multiciliated cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(135488, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0136519', 'increased cell population proliferation in posterior region', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(135489, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0139624', 'decreased cell population proliferation in medial region', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(135490, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0101494', 'abnormal blastomere D1.2.1', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(135491, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0101576', 'abnormal blastomere V1.2.2', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(135492, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0127683', 'abnormally localised centromere', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(135493, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0127196', 'abnormally localised electrically active cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(135494, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0138578', 'decreased cell population proliferation in anatomical system', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(135495, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100415', 'abnormal secretory epithelial cell', 0.52, 3.6715585125471644, 1.3817418089225373, 'UPHENO:0086172', 'abnormal cell'),
(135496, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0101072', 'abnormal mitochondrial cloud', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(135497, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0141798', 'abnormal lipid metabolic process', 0.44, 4.758907843651163, 1.447038165082909, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(135498, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0101241', 'abnormal nucleate erythrocyte', 0.6190476190476191, 3.6715585125471644, 1.5076039119696991, 'UPHENO:0086172', 'abnormal cell'),
(135499, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0136520', 'increased cell population proliferation in dorsal region', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(135500, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0102323', 'abnormal keratin accumulating cell morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(135501, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0102704', 'abnormal mitochondrial cloud morphology', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(135502, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0101500', 'abnormal endodermal cell', 0.48148148148148145, 3.6715585125471644, 1.3295816755533123, 'UPHENO:0086172', 'abnormal cell'),
(135503, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0127435', 'abnormally localised mitotic spindle', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(135504, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100437', 'abnormal proepicardium', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(135505, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0101587', 'abnormal hemangioblast', 0.5, 3.6715585125471644, 1.3549093166236559, 'UPHENO:0086172', 'abnormal cell'),
(135506, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0141264', 'abnormal schooling behavior', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(135507, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100384', 'abnormal amputated tissue', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135508, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0136191', 'increased cell population proliferation in organ part', 0.42857142857142855, 5.835653092541957, 1.5814531869511603, 'HP:0011017', 'Abnormal cellular physiology'),
(135509, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0101921', 'abnormal chondroblast morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(135510, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0101096', 'abnormal tendon', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(135511, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0102147', 'abnormal somatic stem cell morphology', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(135512, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0101132', 'abnormal apoptotic cell', 0.6190476190476191, 3.6715585125471644, 1.5076039119696991, 'UPHENO:0086172', 'abnormal cell'),
(135513, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0102061', 'abnormal spermatid morphology', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(135514, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0101467', 'abnormal alkali secreting cell', 0.6190476190476191, 3.6715585125471644, 1.5076039119696991, 'UPHENO:0086172', 'abnormal cell'),
(135515, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0141777', 'abnormal catabolic process', 0.4782608695652174, 4.758907843651163, 1.508641575552437, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(135516, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0103041', 'abnormal perivitelline space morphology', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(135517, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0131089', 'abnormally increased number of mitotic cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(135518, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0139618', 'decreased cell population proliferation in axial region', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(135519, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100009', 'abnormal multi-tissue structure', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135520, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100317', 'abnormal respiratory system', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(135521, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0138580', 'decreased cell population proliferation in female organism', 0.4166666666666667, 5.835653092541957, 1.5593338712067029, 'HP:0011017', 'Abnormal cellular physiology'),
(135522, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0141497', 'abnormal lymphoblast', 0.5, 3.6715585125471644, 1.3549093166236559, 'UPHENO:0086172', 'abnormal cell'),
(135523, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0131004', 'abnormally increased number of proepicardium', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(135524, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0141289', 'abnormal spindle microtubule morphology', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(135525, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0131347', 'abnormally decreased number of myelin accumulating cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(135526, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100003', 'abnormal organism subdivision', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135527, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100396', 'abnormal dorsal animal hemisphere blastomere', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(135528, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0127364', 'abnormally localised multiciliated cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(135529, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100274', 'abnormal sensory system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(135530, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100901', 'abnormal blastomere D1.2.2', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(135531, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0131278', 'abnormally decreased number of keratin accumulating cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(135532, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100640', 'abnormal notochordal sheath', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(135533, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0131090', 'abnormally increased number of oxygen accumulating cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(135534, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0131031', 'abnormally increased number of nucleate erythrocyte', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(135535, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100701', 'abnormal microglial cell', 0.48148148148148145, 3.6715585125471644, 1.3295816755533123, 'UPHENO:0086172', 'abnormal cell'),
(135536, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0136526', 'increased cell population proliferation in postero-ventral region', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(135537, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0135718', 'increased cell population proliferation in anatomical line', 0.4411764705882353, 5.835653092541957, 1.6045413160604438, 'HP:0011017', 'Abnormal cellular physiology'),
(135538, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100814', 'abnormal natural killer cell', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(135539, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0125384', 'absent ciliated cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(135540, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0102386', 'abnormal electrically active cell morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(135541, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100120', 'abnormal genital system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(135542, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0101575', 'abnormal vitelline membrane', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(135543, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0126314', 'absent absorptive cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(135544, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0142065', 'abnormally decreased number of desmosome', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(135545, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100570', 'abnormal axon', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(135546, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100010', 'abnormal multicellular anatomical structure', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135547, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0136524', 'increased cell population proliferation in antero-ventral region', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(135548, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0103093', 'abnormal sperm entry point morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(135549, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0115505', 'dead whole organism', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135550, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0141786', 'abnormal pigment metabolic process', 0.4782608695652174, 4.758907843651163, 1.508641575552437, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(135551, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100638', 'abnormal polar body', 0.6190476190476191, 3.6715585125471644, 1.5076039119696991, 'UPHENO:0086172', 'abnormal cell'),
(135552, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0127029', 'abnormally localised multiciliated cell precursor', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(135553, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0131389', 'abnormally decreased number of barrier epithelial cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(135554, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100702', 'abnormal glial cell', 0.5, 3.6715585125471644, 1.3549093166236559, 'UPHENO:0086172', 'abnormal cell'),
(135555, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100587', 'abnormal vestibuloauditory system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(135556, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0101326', 'abnormal cementoblast', 0.6190476190476191, 3.6715585125471644, 1.5076039119696991, 'UPHENO:0086172', 'abnormal cell'),
(135557, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0141718', 'abnormal posterior notochord', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(135558, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0107288', 'abnormal larval alimentary system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(135559, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0101297', 'abnormal barrier cell', 0.6190476190476191, 3.6715585125471644, 1.5076039119696991, 'UPHENO:0086172', 'abnormal cell'),
(135560, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100649', 'abnormal growth cone', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(135561, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0141499', 'abnormal tadpole', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135562, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0103129', 'abnormal ciliary axoneme morphology', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(135563, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0101174', 'abnormal articular system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(135564, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0102872', 'abnormal ciliated non-epidermal cell morphology', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(135565, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0101228', 'abnormal mesenchymal stem cell', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(135566, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0124864', 'absent germ cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(135567, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0131654', 'abnormal neuron projection', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(135568, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100704', 'abnormal Merkel cell', 0.6190476190476191, 3.6715585125471644, 1.5076039119696991, 'UPHENO:0086172', 'abnormal cell'),
(135569, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100742', 'abnormal musculoskeletal system', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135570, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100544', 'abnormal neuromast support cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(135571, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100216', 'abnormal hepato-pancreatic progenitor cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(135572, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0107263', 'abnormal anatomical side', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135573, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0101278', 'abnormal pigment cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(135574, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0141791', 'abnormal primary metabolic process', 0.4782608695652174, 4.758907843651163, 1.508641575552437, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(135575, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100423', 'abnormal process', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135576, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0126600', 'abnormally localised progenitor cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(135577, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100732', 'abnormal tendon fibroblast', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(135578, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0107371', 'abnormal migrating myoblast morphology', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(135579, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0107264', 'abnormal anterior side', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135580, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0102768', 'abnormal ooplasm morphology', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(135581, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0133441', 'abnormally increased number of cilium in the ciliated cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(135582, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100676', 'abnormal blastomere D2.2', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(135583, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100960', 'abnormal postmigratory neural crest cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(135584, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0127508', 'abnormally localised barrier epithelial cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(135585, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0101109', 'abnormal egg cell-free extract', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135586, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0131134', 'abnormally increased number of barrier cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(135587, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0107285', 'abnormal flexural organ', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(135588, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0131136', 'abnormally increased number of multiciliated cell precursor', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(135589, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0101461', 'abnormal sperm entry point', 0.5652173913043478, 3.6715585125471644, 1.440565418328227, 'UPHENO:0086172', 'abnormal cell'),
(135590, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100477', 'abnormal pericyte', 0.6190476190476191, 3.6715585125471644, 1.5076039119696991, 'UPHENO:0086172', 'abnormal cell'),
(135591, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0102873', 'abnormal nucleate erythrocyte morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(135592, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0126454', 'abnormally localised stem cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(135593, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100786', 'abnormal presumptive axial mesoderm', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135594, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100802', 'abnormal exocrine cell', 0.6190476190476191, 3.6715585125471644, 1.5076039119696991, 'UPHENO:0086172', 'abnormal cell'),
(135595, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0125854', 'absent barrier epithelial cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(135596, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0126983', 'abnormally localised primordial germ cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(135597, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100151', 'abnormal primordium', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135598, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0126472', 'abnormally localised secondary spermatogonium', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(135599, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0101078', 'abnormal mucous gland', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135600, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0127339', 'abnormally localised migrating myoblast', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(135601, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0127819', 'abnormally localised ciliary axoneme', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(135602, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0138233', 'decreased cell population proliferation in hindlimb region', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(135603, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0125644', 'absent pericyte', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(135604, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0101347', 'abnormal hindlimb region', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135605, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0127338', 'abnormally localised mucus secreting cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(135606, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0141299', 'abnormal actin filament morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(135607, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0127089', 'abnormally localised myoblast', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(135608, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0101061', 'abnormal plasma membrane', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(135609, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100781', 'abnormal presumptive ectoderm', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135610, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0101157', 'abnormal female organism', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135611, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0131247', 'abnormally decreased number of nucleate erythrocyte', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(135612, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0141738', 'abnormal carbon dioxide homeostasis', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(135613, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100888', 'abnormal microtubule', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(135614, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0101480', 'abnormal stage V oocyte', 0.5652173913043478, 3.6715585125471644, 1.440565418328227, 'UPHENO:0086172', 'abnormal cell'),
(135615, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0141263', 'abnormal visually guided collision avoidance behavior', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(135616, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0138262', 'decreased cell population proliferation in embryo', 0.4166666666666667, 5.835653092541957, 1.5593338712067029, 'HP:0011017', 'Abnormal cellular physiology'),
(135617, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0138820', 'decreased cell population proliferation in anatomical line', 0.4411764705882353, 5.835653092541957, 1.6045413160604438, 'HP:0011017', 'Abnormal cellular physiology'),
(135618, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0107323', 'abnormal thrombocyte', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(135619, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0102965', 'abnormal barrier epithelial cell morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(135620, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100724', 'abnormal kinetochore', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(135621, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0141781', 'abnormal secondary metabolic process', 0.4782608695652174, 4.758907843651163, 1.508641575552437, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(135622, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0131559', 'abnormally localised spindle microtubule', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(135623, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100688', 'abnormal adipose tissue', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(135624, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0139500', 'decreased cell population proliferation in egg jelly', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(135625, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0141748', 'abnormal gas homeostasis', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(135626, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0135613', 'increased cell population proliferation in anatomical cluster', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(135627, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0103145', 'abnormal basal body morphology', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(135628, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0102024', 'abnormal cilium morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(135629, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100162', 'abnormal presumptive rhombomere', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135630, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100429', 'abnormal spermatid', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(135631, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100268', 'abnormal circulatory system', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135632, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0127257', 'abnormally localised wedge region', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(135633, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0131669', 'abnormal Roux spot', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(135634, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0127703', 'abnormally localised morula cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(135635, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100715', 'abnormal ciliated cell', 0.6190476190476191, 3.6715585125471644, 1.5076039119696991, 'UPHENO:0086172', 'abnormal cell'),
(135636, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0125454', 'absent myoblast', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(135637, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0127171', 'abnormally localised myelin accumulating cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(135638, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0130989', 'abnormally increased number of ciliated cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(135639, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0101037', 'abnormal hatching gland cell', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(135640, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0125013', 'absent early embryonic cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(135641, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100336', 'abnormal interneuron', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(135642, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0100392', 'abnormal cilium', 0.5652173913043478, 3.6715585125471644, 1.440565418328227, 'UPHENO:0086172', 'abnormal cell'),
(135643, 'HP:4000056', 'Abnormal apoptosis', 'XPO:00000000', 'Xenopus phenotype', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(135644, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0130964', 'abnormally increased number of cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(135645, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0101514', 'abnormal dendrite', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(135646, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0102860', 'abnormal mesenchymal stem cell morphology', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(135647, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0138424', 'decreased cell population proliferation in marginal zone (sensu neural)', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(135648, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0131735', 'abnormal spindle assembly', 0.5172413793103449, 5.835653092541957, 1.7373661832679608, 'HP:0011017', 'Abnormal cellular physiology'),
(135649, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0138818', 'decreased cell population proliferation in portion of organism substance', 0.4411764705882353, 5.835653092541957, 1.6045413160604438, 'HP:0011017', 'Abnormal cellular physiology'),
(135650, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0107253', 'abnormal enteric nervous system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(135651, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0142030', 'abnormally localised desmosome', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(135652, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0139127', 'decreased cell population proliferation in joint region', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(135653, 'HP:4000056', 'Abnormal apoptosis', 'XPO:0131032', 'abnormally increased number of acid secreting cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(135654, 'HP:0040201', 'Simultanapraxia', 'XPO:0100032', 'abnormal nervous system', 0.4642857142857143, 3.94131651835137, 1.3527368387638634, 'UPHENO:0004523', 'abnormal nervous system'),
(135655, 'HP:0040201', 'Simultanapraxia', 'XPO:0100537', 'abnormal medium cavity', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(135656, 'HP:0040201', 'Simultanapraxia', 'XPO:0100858', 'abnormal presumptive midbrain-hindbrain boundary', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(135657, 'HP:0040201', 'Simultanapraxia', 'XPO:0107253', 'abnormal enteric nervous system', 0.4482758620689655, 3.94131651835137, 1.3292091859262085, 'UPHENO:0004523', 'abnormal nervous system'),
(135658, 'HP:0040201', 'Simultanapraxia', 'XPO:0100916', 'abnormal principal cavity', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(135659, 'HP:0040201', 'Simultanapraxia', 'XPO:0100164', 'abnormal neural nucleus', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(135660, 'HP:0040201', 'Simultanapraxia', 'XPO:0100702', 'abnormal glial cell', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(135661, 'HP:0040201', 'Simultanapraxia', 'XPO:0100196', 'abnormal neuron', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(135662, 'HP:0040201', 'Simultanapraxia', 'XPO:0100158', 'abnormal neuromere', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(135663, 'HP:0040201', 'Simultanapraxia', 'XPO:0100587', 'abnormal vestibuloauditory system', 0.43333333333333335, 3.94131651835137, 1.3068679445984308, 'UPHENO:0004523', 'abnormal nervous system'),
(135664, 'HP:0040201', 'Simultanapraxia', 'XPO:0100114', 'abnormal peripheral nervous system', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(135665, 'HP:0040201', 'Simultanapraxia', 'XPO:0142051', 'abnormal cerebrospinal fluid', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(135666, 'HP:0040201', 'Simultanapraxia', 'XPO:0100274', 'abnormal sensory system', 0.4482758620689655, 3.94131651835137, 1.3292091859262085, 'UPHENO:0004523', 'abnormal nervous system'),
(135667, 'HP:0040201', 'Simultanapraxia', 'XPO:0100175', 'abnormal migrating neuroblast', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(135668, 'HP:0040201', 'Simultanapraxia', 'XPO:0100031', 'abnormal central nervous system', 0.4482758620689655, 3.94131651835137, 1.3292091859262085, 'UPHENO:0004523', 'abnormal nervous system'),
(135669, 'HP:0040201', 'Simultanapraxia', 'XPO:0101501', 'abnormal parabrachial area', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(135670, 'HP:0040201', 'Simultanapraxia', 'XPO:0100642', 'abnormal gustatory system', 0.43333333333333335, 3.94131651835137, 1.3068679445984308, 'UPHENO:0004523', 'abnormal nervous system'),
(135671, 'HP:0040201', 'Simultanapraxia', 'XPO:0100427', 'abnormal olfactory system', 0.43333333333333335, 3.94131651835137, 1.3068679445984308, 'UPHENO:0004523', 'abnormal nervous system'),
(135672, 'HP:0040201', 'Simultanapraxia', 'XPO:0100273', 'abnormal visual system', 0.43333333333333335, 3.94131651835137, 1.3068679445984308, 'UPHENO:0004523', 'abnormal nervous system'),
(135673, 'HP:0025429', 'Abnormal cry', 'XPO:0141267', 'abnormal resting posture', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(135674, 'HP:0025429', 'Abnormal cry', 'XPO:0100913', 'abnormal Brachets cleft', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135675, 'HP:0025429', 'Abnormal cry', 'XPO:0100721', 'abnormal centromere', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(135676, 'HP:0025429', 'Abnormal cry', 'XPO:0101029', 'abnormal right spleen primordium', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(135677, 'HP:0025429', 'Abnormal cry', 'XPO:0101136', 'abnormal ooplasm', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(135678, 'HP:0025429', 'Abnormal cry', 'XPO:0100383', 'abnormal amputated fin', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135679, 'HP:0025429', 'Abnormal cry', 'XPO:0100707', 'abnormal central vegetal yolk mass', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135680, 'HP:0025429', 'Abnormal cry', 'XPO:0100581', 'abnormal immune system', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(135681, 'HP:0025429', 'Abnormal cry', 'XPO:0100549', 'abnormal mitotic cell', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(135682, 'HP:0025429', 'Abnormal cry', 'XPO:0100025', 'abnormal oocyte', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(135683, 'HP:0025429', 'Abnormal cry', 'XPO:0100727', 'abnormal odontogenic papilla', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(135684, 'HP:0025429', 'Abnormal cry', 'XPO:0100437', 'abnormal proepicardium', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(135685, 'HP:0025429', 'Abnormal cry', 'XPO:0100985', 'abnormal simple columnar epithelium', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135686, 'HP:0025429', 'Abnormal cry', 'XPO:0100786', 'abnormal presumptive axial mesoderm', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135687, 'HP:0025429', 'Abnormal cry', 'XPO:0100734', 'abnormal lateral line system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(135688, 'HP:0025429', 'Abnormal cry', 'XPO:0100912', 'abnormal trabecula', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135689, 'HP:0025429', 'Abnormal cry', 'XPO:0100232', 'abnormal lymphatic system', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(135690, 'HP:0025429', 'Abnormal cry', 'XPO:0141778', 'abnormal biosynthetic process', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(135691, 'HP:0025429', 'Abnormal cry', 'XPO:0115508', 'abnormally peramorphic growth of whole organism', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135692, 'HP:0025429', 'Abnormal cry', 'XPO:0131666', 'abnormal adherens junction', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(135693, 'HP:0025429', 'Abnormal cry', 'XPO:0101133', 'abnormal motor neuron', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(135694, 'HP:0025429', 'Abnormal cry', 'XPO:0100664', 'abnormal periocular region', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(135695, 'HP:0025429', 'Abnormal cry', 'XPO:0100860', 'abnormal parathyroid', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(135696, 'HP:0025429', 'Abnormal cry', 'XPO:0107326', 'abnormal regenerating pelvic girdle', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135697, 'HP:0025429', 'Abnormal cry', 'XPO:0100308', 'abnormal early embryonic cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(135698, 'HP:0025429', 'Abnormal cry', 'XPO:0100104', 'abnormal embryonic structure', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135699, 'HP:0025429', 'Abnormal cry', 'XPO:0131723', 'abnormal pathway-restricted SMAD protein phosphorylation', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(135700, 'HP:0025429', 'Abnormal cry', 'XPO:0100282', 'abnormal pelvic girdle primordium', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135701, 'HP:0025429', 'Abnormal cry', 'XPO:0107262', 'abnormal left-right axis', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135702, 'HP:0025429', 'Abnormal cry', 'XPO:0107284', 'abnormal migrating myoblast', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(135703, 'HP:0025429', 'Abnormal cry', 'XPO:0100486', 'abnormal oral evagination', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(135704, 'HP:0025429', 'Abnormal cry', 'XPO:0100023', 'abnormal mesenchyme', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135705, 'HP:0025429', 'Abnormal cry', 'XPO:0101349', 'abnormal trunk region', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135706, 'HP:0025429', 'Abnormal cry', 'XPO:0141791', 'abnormal primary metabolic process', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(135707, 'HP:0025429', 'Abnormal cry', 'XPO:0100231', 'abnormal compound organ', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135708, 'HP:0025429', 'Abnormal cry', 'XPO:0100546', 'abnormal whole organism', 0.5294117647058824, 1.706362323152461, 0.9504568842024205, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135709, 'HP:0025429', 'Abnormal cry', 'XPO:0100449', 'abnormal lymphocyte', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(135710, 'HP:0025429', 'Abnormal cry', 'XPO:0100791', 'abnormal multiciliated cell precursor', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(135711, 'HP:0025429', 'Abnormal cry', 'XPO:0100339', 'abnormal circumblastoporal collar', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135712, 'HP:0025429', 'Abnormal cry', 'XPO:0100377', 'abnormal connective tissue', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(135713, 'HP:0025429', 'Abnormal cry', 'XPO:0115512', 'abnormally semi-erect whole organism', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135714, 'HP:0025429', 'Abnormal cry', 'XPO:0141786', 'abnormal pigment metabolic process', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(135715, 'HP:0025429', 'Abnormal cry', 'XPO:0100228', 'abnormal skeletal subdivision', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(135716, 'HP:0025429', 'Abnormal cry', 'XPO:0100551', 'abnormal oocyte cortex', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(135717, 'HP:0025429', 'Abnormal cry', 'XPO:0141775', 'abnormal nitrogen compound metabolic process', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(135718, 'HP:0025429', 'Abnormal cry', 'XPO:0101023', 'abnormal ultimobranchial body', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(135719, 'HP:0025429', 'Abnormal cry', 'XPO:0100084', 'abnormal anatomical group', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135720, 'HP:0025429', 'Abnormal cry', 'XPO:0107268', 'abnormal left side', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135721, 'HP:0025429', 'Abnormal cry', 'XPO:0101468', 'abnormal stage I oocyte', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(135722, 'HP:0025429', 'Abnormal cry', 'XPO:0101302', 'abnormal subcortical cytoplasm', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(135723, 'HP:0025429', 'Abnormal cry', 'XPO:0101297', 'abnormal barrier cell', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(135724, 'HP:0025429', 'Abnormal cry', 'XPO:0100715', 'abnormal ciliated cell', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(135725, 'HP:0025429', 'Abnormal cry', 'XPO:0100587', 'abnormal vestibuloauditory system', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(135726, 'HP:0025429', 'Abnormal cry', 'XPO:0100156', 'abnormal foregut', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(135727, 'HP:0025429', 'Abnormal cry', 'XPO:0101406', 'abnormal cleavage furrow', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135728, 'HP:0025429', 'Abnormal cry', 'XPO:0101241', 'abnormal nucleate erythrocyte', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(135729, 'HP:0025429', 'Abnormal cry', 'XPO:0100014', 'abnormal tissue', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135730, 'HP:0025429', 'Abnormal cry', 'XPO:0100151', 'abnormal primordium', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135731, 'HP:0025429', 'Abnormal cry', 'XPO:0100640', 'abnormal notochordal sheath', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(135732, 'HP:0025429', 'Abnormal cry', 'XPO:0100433', 'abnormal pectoral appendage', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135733, 'HP:0025429', 'Abnormal cry', 'XPO:0101460', 'abnormal fibrocellular pad', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135734, 'HP:0025429', 'Abnormal cry', 'XPO:0107258', 'abnormal anatomical axis', 0.5294117647058824, 1.706362323152461, 0.9504568842024205, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135735, 'HP:0025429', 'Abnormal cry', 'XPO:0131691', 'abnormal molecular function', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(135736, 'HP:0025429', 'Abnormal cry', 'XPO:0100887', 'abnormal right-dorsal blastomere', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(135737, 'HP:0025429', 'Abnormal cry', 'XPO:0100802', 'abnormal exocrine cell', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(135738, 'HP:0025429', 'Abnormal cry', 'XPO:0100864', 'abnormal dorsolateral ascending neuron', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(135739, 'HP:0025429', 'Abnormal cry', 'XPO:0142051', 'abnormal cerebrospinal fluid', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(135740, 'HP:0025429', 'Abnormal cry', 'XPO:0141497', 'abnormal lymphoblast', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(135741, 'HP:0025429', 'Abnormal cry', 'XPO:0101405', 'abnormal ring structure', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(135742, 'HP:0025429', 'Abnormal cry', 'XPO:0141315', 'abnormal anatomical region', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135743, 'HP:0025429', 'Abnormal cry', 'XPO:0100956', 'abnormal centrosome', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(135744, 'HP:0025429', 'Abnormal cry', 'XPO:0100152', 'abnormal alimentary system', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(135745, 'HP:0025429', 'Abnormal cry', 'XPO:0100120', 'abnormal genital system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(135746, 'HP:0025429', 'Abnormal cry', 'XPO:0124719', 'absent anatomical structure', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135747, 'HP:0025429', 'Abnormal cry', 'XPO:0100189', 'abnormal enteroendocrine cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(135748, 'HP:0025429', 'Abnormal cry', 'XPO:0100482', 'abnormal Mullerian duct', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(135749, 'HP:0025429', 'Abnormal cry', 'XPO:0100402', 'abnormal zeugopod', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(135750, 'HP:0025429', 'Abnormal cry', 'XPO:0101269', 'abnormal mesodermal cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(135751, 'HP:0025429', 'Abnormal cry', 'XPO:0100573', 'abnormal extraembryonic structure', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135752, 'HP:0025429', 'Abnormal cry', 'XPO:0142054', 'abnormal digestive tract', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(135753, 'HP:0025429', 'Abnormal cry', 'XPO:0107267', 'abnormal ventral side', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135754, 'HP:0025429', 'Abnormal cry', 'XPO:0100667', 'abnormal vegetal yolk mass', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135755, 'HP:0025429', 'Abnormal cry', 'XPO:0100574', 'abnormal gastrula cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(135756, 'HP:0025429', 'Abnormal cry', 'XPO:0100158', 'abnormal neuromere', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(135757, 'HP:0025429', 'Abnormal cry', 'XPO:0100003', 'abnormal organism subdivision', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135758, 'HP:0025429', 'Abnormal cry', 'XPO:0141276', 'decreased surface breathing', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(135759, 'HP:0025429', 'Abnormal cry', 'XPO:0100317', 'abnormal respiratory system', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(135760, 'HP:0025429', 'Abnormal cry', 'XPO:0101132', 'abnormal apoptotic cell', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(135761, 'HP:0025429', 'Abnormal cry', 'XPO:0100894', 'abnormal nucleus', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(135762, 'HP:0025429', 'Abnormal cry', 'XPO:0141809', 'abnormal catalytic activity', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(135763, 'HP:0025429', 'Abnormal cry', 'XPO:0107311', 'abnormal apical junction complex', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(135764, 'HP:0025429', 'Abnormal cry', 'XPO:0141263', 'abnormal visually guided collision avoidance behavior', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(135765, 'HP:0025429', 'Abnormal cry', 'XPO:0100196', 'abnormal neuron', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(135766, 'HP:0025429', 'Abnormal cry', 'XPO:0101096', 'abnormal tendon', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(135767, 'HP:0025429', 'Abnormal cry', 'XPO:0107273', 'abnormal basal region', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135768, 'HP:0025429', 'Abnormal cry', 'XPO:0100843', 'abnormal fasciculated network of fibrils', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(135769, 'HP:0025429', 'Abnormal cry', 'XPO:0141738', 'abnormal carbon dioxide homeostasis', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(135770, 'HP:0025429', 'Abnormal cry', 'XPO:0100427', 'abnormal olfactory system', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(135771, 'HP:0025429', 'Abnormal cry', 'XPO:0100255', 'abnormal pelvic appendage', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135772, 'HP:0025429', 'Abnormal cry', 'XPO:0141792', 'abnormal small molecule metabolic process', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(135773, 'HP:0025429', 'Abnormal cry', 'XPO:0107253', 'abnormal enteric nervous system', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(135774, 'HP:0025429', 'Abnormal cry', 'XPO:0100256', 'abnormal paired appendage', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135775, 'HP:0025429', 'Abnormal cry', 'XPO:0141265', 'abnormal escape behavior', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(135776, 'HP:0025429', 'Abnormal cry', 'XPO:0101224', 'abnormal dorsal involuting marginal zone', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135777, 'HP:0025429', 'Abnormal cry', 'XPO:0133388', 'absent insulin receptor signaling pathway', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(135778, 'HP:0025429', 'Abnormal cry', 'XPO:0101448', 'abnormal myelin accumulating cell', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(135779, 'HP:0025429', 'Abnormal cry', 'XPO:0100372', 'abnormal hematological system', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(135780, 'HP:0025429', 'Abnormal cry', 'XPO:0133403', 'abnormal developmental process', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(135781, 'HP:0025429', 'Abnormal cry', 'XPO:0100760', 'abnormal Stirnorgan', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(135782, 'HP:0025429', 'Abnormal cry', 'XPO:0101228', 'abnormal mesenchymal stem cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(135783, 'HP:0025429', 'Abnormal cry', 'XPO:0100533', 'abnormal melanoblast', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(135784, 'HP:0025429', 'Abnormal cry', 'XPO:0100872', 'abnormal neuroendocrine cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(135785, 'HP:0025429', 'Abnormal cry', 'XPO:0141771', 'abnormal urea homeostasis', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(135786, 'HP:0025429', 'Abnormal cry', 'XPO:0100172', 'abnormal stem cell', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(135787, 'HP:0025429', 'Abnormal cry', 'XPO:0115758', 'abnormally decreased mobility of melanoblast', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(135788, 'HP:0025429', 'Abnormal cry', 'XPO:0131725', 'abnormal phosphorylation of RNA polymerase II C-terminal domain', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(135789, 'HP:0025429', 'Abnormal cry', 'XPO:0142056', 'abnormal main body axis', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135790, 'HP:0025429', 'Abnormal cry', 'XPO:0100503', 'abnormal blastomere D2', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(135791, 'HP:0025429', 'Abnormal cry', 'XPO:0100935', 'abnormal skeleton', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(135792, 'HP:0025429', 'Abnormal cry', 'XPO:0100207', 'abnormal blastema', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135793, 'HP:0025429', 'Abnormal cry', 'XPO:0125007', 'absent anatomical line', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135794, 'HP:0025429', 'Abnormal cry', 'XPO:0100741', 'abnormal blastopore', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135795, 'HP:0025429', 'Abnormal cry', 'XPO:0141790', 'abnormal cellular metabolic process', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(135796, 'HP:0025429', 'Abnormal cry', 'XPO:0101519', 'abnormal hypobranchial placode', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135797, 'HP:0025429', 'Abnormal cry', 'XPO:0100915', 'abnormal dermal system', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135798, 'HP:0025429', 'Abnormal cry', 'XPO:0100547', 'abnormal blastomere V2', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(135799, 'HP:0025429', 'Abnormal cry', 'XPO:0100398', 'abnormal vegetal blastomere', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(135800, 'HP:0025429', 'Abnormal cry', 'XPO:0101377', 'abnormal manicotto glandulare', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(135801, 'HP:0025429', 'Abnormal cry', 'XPO:0131685', 'abnormal cortical actin cytoskeleton', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(135802, 'HP:0025429', 'Abnormal cry', 'XPO:0100164', 'abnormal neural nucleus', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(135803, 'HP:0025429', 'Abnormal cry', 'XPO:0100846', 'abnormal hindlimb', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(135804, 'HP:0025429', 'Abnormal cry', 'XPO:0100376', 'abnormal animal pole', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135805, 'HP:0025429', 'Abnormal cry', 'XPO:0141600', 'absent metamorphosis', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(135806, 'HP:0025429', 'Abnormal cry', 'XPO:0100899', 'abnormal secondary spermatogonium', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(135807, 'HP:0025429', 'Abnormal cry', 'XPO:0141904', 'abnormal glucosamine metabolic process', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(135808, 'HP:0025429', 'Abnormal cry', 'XPO:0101109', 'abnormal egg cell-free extract', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135809, 'HP:0025429', 'Abnormal cry', 'XPO:0100176', 'abnormal stage VI oocyte', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(135810, 'HP:0025429', 'Abnormal cry', 'XPO:0100515', 'abnormal somatic stem cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(135811, 'HP:0025429', 'Abnormal cry', 'XPO:0141781', 'abnormal secondary metabolic process', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(135812, 'HP:0025429', 'Abnormal cry', 'XPO:0141272', 'absent surface breathing', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(135813, 'HP:0025429', 'Abnormal cry', 'XPO:0100954', 'abnormal neural progenitor cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(135814, 'HP:0025429', 'Abnormal cry', 'XPO:0101366', 'abnormal morula cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(135815, 'HP:0025429', 'Abnormal cry', 'XPO:0100004', 'abnormal cell', 0.55, 1.8210412618256888, 1.0007860380741376, 'HP:0000118', 'Phenotypic abnormality'),
(135816, 'HP:0025429', 'Abnormal cry', 'XPO:0100728', 'abnormal cell condensation', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135817, 'HP:0025429', 'Abnormal cry', 'XPO:0101740', 'abnormal cell part morphology', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(135818, 'HP:0025429', 'Abnormal cry', 'XPO:0101577', 'abnormal notochordal epithelium', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135819, 'HP:0025429', 'Abnormal cry', 'XPO:0141264', 'abnormal schooling behavior', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(135820, 'HP:0025429', 'Abnormal cry', 'XPO:0100545', 'abnormal male organism', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135821, 'HP:0025429', 'Abnormal cry', 'XPO:0101083', 'abnormal T cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(135822, 'HP:0025429', 'Abnormal cry', 'XPO:0100162', 'abnormal presumptive rhombomere', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135823, 'HP:0025429', 'Abnormal cry', 'XPO:0101078', 'abnormal mucous gland', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135824, 'HP:0025429', 'Abnormal cry', 'XPO:0100309', 'abnormal vegetal hemisphere', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135825, 'HP:0025429', 'Abnormal cry', 'XPO:0115566', 'abnormal variability of size of forelimb', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(135826, 'HP:0025429', 'Abnormal cry', 'XPO:0141777', 'abnormal catabolic process', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(135827, 'HP:0025429', 'Abnormal cry', 'XPO:0101373', 'abnormal oxygen accumulating cell', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(135828, 'HP:0025429', 'Abnormal cry', 'XPO:0100917', 'abnormal stage III oocyte', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(135829, 'HP:0025429', 'Abnormal cry', 'XPO:0100890', 'abnormal pharyngeal cavity', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(135830, 'HP:0025429', 'Abnormal cry', 'XPO:0100403', 'abnormal forelimb', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(135831, 'HP:0025429', 'Abnormal cry', 'XPO:0100289', 'abnormal chondroblast', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(135832, 'HP:0025429', 'Abnormal cry', 'XPO:0100868', 'abnormal transporting epithelium', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135833, 'HP:0025429', 'Abnormal cry', 'XPO:0100423', 'abnormal process', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135834, 'HP:0025429', 'Abnormal cry', 'XPO:0141798', 'abnormal lipid metabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(135835, 'HP:0025429', 'Abnormal cry', 'XPO:0107285', 'abnormal flexural organ', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(135836, 'HP:0025429', 'Abnormal cry', 'XPO:0141794', 'abnormal prosthetic group metabolic process', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(135837, 'HP:0025429', 'Abnormal cry', 'XPO:0100762', 'abnormal intersomitic region', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135838, 'HP:0025429', 'Abnormal cry', 'XPO:0100386', 'abnormal limb', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(135839, 'HP:0025429', 'Abnormal cry', 'XPO:0141796', 'abnormal demethylation', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(135840, 'HP:0025429', 'Abnormal cry', 'XPO:0100265', 'abnormal sensory epithelial cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(135841, 'HP:0025429', 'Abnormal cry', 'XPO:0100976', 'abnormal multiciliated cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(135842, 'HP:0025429', 'Abnormal cry', 'XPO:0101472', 'abnormal zygote cortex', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(135843, 'HP:0025429', 'Abnormal cry', 'XPO:0100999', 'abnormal serous membrane', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135844, 'HP:0025429', 'Abnormal cry', 'XPO:0100363', 'abnormal cardiovascular system', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135845, 'HP:0025429', 'Abnormal cry', 'XPO:0101450', 'abnormal myeloid cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(135846, 'HP:0025429', 'Abnormal cry', 'XPO:0101162', 'abnormal stromal cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(135847, 'HP:0025429', 'Abnormal cry', 'XPO:0131469', 'abnormal heart process', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(135848, 'HP:0025429', 'Abnormal cry', 'XPO:0101498', 'abnormal stage II oocyte', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(135849, 'HP:0025429', 'Abnormal cry', 'XPO:0100481', 'abnormal anatomical line', 0.5625, 1.706362323152461, 0.9797085315405084, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135850, 'HP:0025429', 'Abnormal cry', 'XPO:0107271', 'abnormal apical region', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135851, 'HP:0025429', 'Abnormal cry', 'XPO:0141797', 'abnormal hydrogen metabolic process', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(135852, 'HP:0025429', 'Abnormal cry', 'XPO:0100726', 'abnormal tail', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135853, 'HP:0025429', 'Abnormal cry', 'XPO:0100991', 'abnormal iliac process primordium', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135854, 'HP:0025429', 'Abnormal cry', 'XPO:0102113', 'abnormal anatomical line morphology', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135855, 'HP:0025429', 'Abnormal cry', 'XPO:0100002', 'abnormal head', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(135856, 'HP:0025429', 'Abnormal cry', 'XPO:0101107', 'abnormal erythroid cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(135857, 'HP:0025429', 'Abnormal cry', 'XPO:0101503', 'abnormal organ cortex', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135858, 'HP:0025429', 'Abnormal cry', 'XPO:0100285', 'abnormal progenitor cell', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(135859, 'HP:0025429', 'Abnormal cry', 'XPO:0100553', 'abnormal laryngeal muscle primordium', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135860, 'HP:0025429', 'Abnormal cry', 'XPO:0107272', 'abnormal axial region', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135861, 'HP:0025429', 'Abnormal cry', 'XPO:0101283', 'abnormal left-ventral blastomere', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(135862, 'HP:0025429', 'Abnormal cry', 'XPO:0101378', 'abnormal blastomere D1', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(135863, 'HP:0025429', 'Abnormal cry', 'XPO:0100225', 'abnormal endocrine system', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(135864, 'HP:0025429', 'Abnormal cry', 'XPO:0100277', 'abnormal blastocoel', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135865, 'HP:0025429', 'Abnormal cry', 'XPO:0101074', 'abnormal germinal vesicle', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(135866, 'HP:0025429', 'Abnormal cry', 'XPO:0100616', 'abnormal ventral blood island', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(135867, 'HP:0025429', 'Abnormal cry', 'XPO:0131667', 'abnormal actin cytoskeleton', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(135868, 'HP:0025429', 'Abnormal cry', 'XPO:0101092', 'abnormal dorso-lateral marginal zone', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135869, 'HP:0025429', 'Abnormal cry', 'XPO:0101451', 'abnormal dorsal lymph space', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(135870, 'HP:0025429', 'Abnormal cry', 'XPO:0100059', 'abnormal regenerating tail', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135871, 'HP:0025429', 'Abnormal cry', 'XPO:0101435', 'abnormal paracrine cell', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(135872, 'HP:0025429', 'Abnormal cry', 'XPO:0100175', 'abnormal migrating neuroblast', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(135873, 'HP:0025429', 'Abnormal cry', 'XPO:0100800', 'abnormal ventral marginal zone', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135874, 'HP:0025429', 'Abnormal cry', 'XPO:0101362', 'abnormal vegetal cortex', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(135875, 'HP:0025429', 'Abnormal cry', 'XPO:0100638', 'abnormal polar body', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(135876, 'HP:0025429', 'Abnormal cry', 'XPO:0115509', 'abnormally semi-viable whole organism', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135877, 'HP:0025429', 'Abnormal cry', 'XPO:0101311', 'abnormal bottle cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(135878, 'HP:0025429', 'Abnormal cry', 'XPO:0141714', 'abnormal anterior notochord', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(135879, 'HP:0025429', 'Abnormal cry', 'XPO:0100378', 'abnormal perichondrium', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(135880, 'HP:0025429', 'Abnormal cry', 'XPO:0101187', 'abnormal dorsolateral commissural neuron', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(135881, 'HP:0025429', 'Abnormal cry', 'XPO:0100585', 'abnormal elastica externa', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(135882, 'HP:0025429', 'Abnormal cry', 'XPO:0100416', 'abnormal ligament', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(135883, 'HP:0025429', 'Abnormal cry', 'XPO:0101497', 'abnormal ciliary axoneme', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(135884, 'HP:0025429', 'Abnormal cry', 'XPO:0101010', 'abnormal dorsal marginal zone', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135885, 'HP:0025429', 'Abnormal cry', 'XPO:0101570', 'abnormal forelimb region', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135886, 'HP:0025429', 'Abnormal cry', 'XPO:0116434', 'abnormal biological process', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(135887, 'HP:0025429', 'Abnormal cry', 'XPO:0101057', 'abnormal vegetal pole', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135888, 'HP:0025429', 'Abnormal cry', 'XPO:0101221', 'abnormal larval immune system', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(135889, 'HP:0025429', 'Abnormal cry', 'XPO:0100907', 'abnormal cytoplasm', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(135890, 'HP:0025429', 'Abnormal cry', 'XPO:0100781', 'abnormal presumptive ectoderm', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135891, 'HP:0025429', 'Abnormal cry', 'XPO:0107265', 'abnormal posterior side', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135892, 'HP:0025429', 'Abnormal cry', 'XPO:0100537', 'abnormal medium cavity', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(135893, 'HP:0025429', 'Abnormal cry', 'XPO:0101240', 'abnormal ciliated non-epidermal cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(135894, 'HP:0025429', 'Abnormal cry', 'XPO:0100093', 'abnormal simple squamous epithelium', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135895, 'HP:0025429', 'Abnormal cry', 'XPO:0101409', 'abnormal perivitelline space', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(135896, 'HP:0025429', 'Abnormal cry', 'XPO:0100799', 'abnormal genital ridge', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(135897, 'HP:0025429', 'Abnormal cry', 'XPO:0100146', 'abnormal primary germ layer', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135898, 'HP:0025429', 'Abnormal cry', 'XPO:0126318', 'abnormally localised cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(135899, 'HP:0025429', 'Abnormal cry', 'XPO:0100465', 'abnormal skeletal system', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(135900, 'HP:0025429', 'Abnormal cry', 'XPO:0101518', 'abnormal B cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(135901, 'HP:0025429', 'Abnormal cry', 'XPO:0107263', 'abnormal anatomical side', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135902, 'HP:0025429', 'Abnormal cry', 'XPO:0100458', 'abnormal autopod', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(135903, 'HP:0025429', 'Abnormal cry', 'XPO:0131687', 'abnormal astral microtubule', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(135904, 'HP:0025429', 'Abnormal cry', 'XPO:0101396', 'abnormal apical epithelial cap', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135905, 'HP:0025429', 'Abnormal cry', 'XPO:0101403', 'abnormal basal lamina', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135906, 'HP:0025429', 'Abnormal cry', 'XPO:0100100', 'abnormal muscle', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(135907, 'HP:0025429', 'Abnormal cry', 'XPO:0100807', 'abnormal matrix-based tissue', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135908, 'HP:0025429', 'Abnormal cry', 'XPO:0100069', 'abnormal urinary system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(135909, 'HP:0025429', 'Abnormal cry', 'XPO:0107259', 'abnormal animal-vegetal axis', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135910, 'HP:0025429', 'Abnormal cry', 'XPO:0100205', 'abnormal limb segment', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(135911, 'HP:0025429', 'Abnormal cry', 'XPO:0100081', 'abnormal anatomical entity in vitro', 0.5625, 1.706362323152461, 0.9797085315405084, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135912, 'HP:0025429', 'Abnormal cry', 'XPO:0100724', 'abnormal kinetochore', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(135913, 'HP:0025429', 'Abnormal cry', 'XPO:0101490', 'abnormal ectodermal cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(135914, 'HP:0025429', 'Abnormal cry', 'XPO:0141772', 'abnormal water homeostasis', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(135915, 'HP:0025429', 'Abnormal cry', 'XPO:0100735', 'abnormal hindgut', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(135916, 'HP:0025429', 'Abnormal cry', 'XPO:0100337', 'abnormal zygote', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(135917, 'HP:0025429', 'Abnormal cry', 'XPO:0100688', 'abnormal adipose tissue', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(135918, 'HP:0025429', 'Abnormal cry', 'XPO:0100501', 'abnormal urogenital system', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(135919, 'HP:0025429', 'Abnormal cry', 'XPO:0100444', 'abnormal cement gland', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135920, 'HP:0025429', 'Abnormal cry', 'XPO:0100687', 'abnormal periotic region', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(135921, 'HP:0025429', 'Abnormal cry', 'XPO:0100393', 'abnormal involuting marginal zone', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135922, 'HP:0025429', 'Abnormal cry', 'XPO:0101149', 'abnormal amputated limb', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135923, 'HP:0025429', 'Abnormal cry', 'XPO:0100523', 'abnormal midgut', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(135924, 'HP:0025429', 'Abnormal cry', 'XPO:0115391', 'abnormally undifferentiated alimentary system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(135925, 'HP:0025429', 'Abnormal cry', 'XPO:0100267', 'abnormal wound epidermis', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135926, 'HP:0025429', 'Abnormal cry', 'XPO:0101535', 'abnormal absorptive cell', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(135927, 'HP:0025429', 'Abnormal cry', 'XPO:0100605', 'abnormal prechordal plate', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135928, 'HP:0025429', 'Abnormal cry', 'XPO:0100201', 'abnormal cavitated compound organ', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135929, 'HP:0025429', 'Abnormal cry', 'XPO:0101264', 'abnormal mitotic spindle', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(135930, 'HP:0025429', 'Abnormal cry', 'XPO:0101411', 'abnormal marginal zone (sensu neural)', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135931, 'HP:0025429', 'Abnormal cry', 'XPO:0100384', 'abnormal amputated tissue', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135932, 'HP:0025429', 'Abnormal cry', 'XPO:0100702', 'abnormal glial cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(135933, 'HP:0025429', 'Abnormal cry', 'XPO:00000000', 'Xenopus phenotype', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(135934, 'HP:0025429', 'Abnormal cry', 'XPO:0100268', 'abnormal circulatory system', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135935, 'HP:0025429', 'Abnormal cry', 'XPO:0100511', 'abnormal stylopod', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(135936, 'HP:0025429', 'Abnormal cry', 'XPO:0101547', 'abnormal lampbrush chromosome', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(135937, 'HP:0025429', 'Abnormal cry', 'XPO:0101589', 'abnormal blastocoel roof', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135938, 'HP:0025429', 'Abnormal cry', 'XPO:0100344', 'abnormal portion of organism substance', 0.5625, 1.706362323152461, 0.9797085315405084, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135939, 'HP:0025429', 'Abnormal cry', 'XPO:0100862', 'abnormal blastomere V1', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(135940, 'HP:0025429', 'Abnormal cry', 'XPO:0141718', 'abnormal posterior notochord', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(135941, 'HP:0025429', 'Abnormal cry', 'XPO:0107312', 'abnormal filopodium', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(135942, 'HP:0025429', 'Abnormal cry', 'XPO:0100293', 'abnormal duct', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135943, 'HP:0025429', 'Abnormal cry', 'XPO:0100701', 'abnormal microglial cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(135944, 'HP:0025429', 'Abnormal cry', 'XPO:0100274', 'abnormal sensory system', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(135945, 'HP:0025429', 'Abnormal cry', 'XPO:0127101', 'abnormally localised portion of organism substance', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135946, 'HP:0025429', 'Abnormal cry', 'XPO:0141782', 'abnormal methylation', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(135947, 'HP:0025429', 'Abnormal cry', 'XPO:0100858', 'abnormal presumptive midbrain-hindbrain boundary', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(135948, 'HP:0025429', 'Abnormal cry', 'XPO:0101501', 'abnormal parabrachial area', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(135949, 'HP:0025429', 'Abnormal cry', 'XPO:0141748', 'abnormal gas homeostasis', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(135950, 'HP:0025429', 'Abnormal cry', 'XPO:0101976', 'abnormal portion of organism substance morphology', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135951, 'HP:0025429', 'Abnormal cry', 'XPO:0101200', 'abnormal joint region', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135952, 'HP:0025429', 'Abnormal cry', 'XPO:0142052', 'abnormal nasal region', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(135953, 'HP:0025429', 'Abnormal cry', 'XPO:0100540', 'abnormal left lymph heart', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(135954, 'HP:0025429', 'Abnormal cry', 'XPO:0115362', 'abnormally decreased adhesivity of prechordal plate', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135955, 'HP:0025429', 'Abnormal cry', 'XPO:0101543', 'abnormal external gill', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(135956, 'HP:0025429', 'Abnormal cry', 'XPO:0107278', 'abnormal medial region', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135957, 'HP:0025429', 'Abnormal cry', 'XPO:0101174', 'abnormal articular system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(135958, 'HP:0025429', 'Abnormal cry', 'XPO:0100827', 'abnormal atypical epithelium', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135959, 'HP:0025429', 'Abnormal cry', 'XPO:0100722', 'abnormal barbel', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135960, 'HP:0025429', 'Abnormal cry', 'XPO:0101040', 'abnormal axial mesoderm', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135961, 'HP:0025429', 'Abnormal cry', 'XPO:0101113', 'abnormal stage IV oocyte', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(135962, 'HP:0025429', 'Abnormal cry', 'XPO:0101157', 'abnormal female organism', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135963, 'HP:0025429', 'Abnormal cry', 'XPO:0141907', 'abnormal putrescine metabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(135964, 'HP:0025429', 'Abnormal cry', 'XPO:0142057', 'abnormal desmosome', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(135965, 'HP:0025429', 'Abnormal cry', 'XPO:0100842', 'abnormal left-dorsal blastomere', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(135966, 'HP:0025429', 'Abnormal cry', 'XPO:0100745', 'abnormal anterior lymph sac', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(135967, 'HP:0025429', 'Abnormal cry', 'XPO:0141783', 'abnormal collagen metabolic process', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(135968, 'HP:0025429', 'Abnormal cry', 'XPO:0101533', 'abnormal simple cuboidal epithelium', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135969, 'HP:0025429', 'Abnormal cry', 'XPO:0100067', 'abnormal animal hemisphere', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135970, 'HP:0025429', 'Abnormal cry', 'XPO:0101713', 'abnormal anatomical entity in vitro morphology', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135971, 'HP:0025429', 'Abnormal cry', 'XPO:0100691', 'abnormal keratin accumulating cell', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(135972, 'HP:0025429', 'Abnormal cry', 'XPO:0100742', 'abnormal musculoskeletal system', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135973, 'HP:0025429', 'Abnormal cry', 'XPO:0126624', 'abnormally localised anatomical line', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135974, 'HP:0025429', 'Abnormal cry', 'XPO:0101237', 'abnormal mucus secreting cell', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(135975, 'HP:0025429', 'Abnormal cry', 'XPO:0141271', 'increased surface breathing', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(135976, 'HP:0025429', 'Abnormal cry', 'XPO:0100989', 'abnormal right blastomere', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(135977, 'HP:0025429', 'Abnormal cry', 'XPO:0141743', 'abnormal chemical homeostasis within a tissue', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(135978, 'HP:0025429', 'Abnormal cry', 'XPO:0100852', 'abnormal interdigital region', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(135979, 'HP:0025429', 'Abnormal cry', 'XPO:0101461', 'abnormal sperm entry point', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(135980, 'HP:0025429', 'Abnormal cry', 'XPO:0101099', 'abnormal ventro-lateral marginal zone', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135981, 'HP:0025429', 'Abnormal cry', 'XPO:0100477', 'abnormal pericyte', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(135982, 'HP:0025429', 'Abnormal cry', 'XPO:0100665', 'abnormal egg jelly', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135983, 'HP:0025429', 'Abnormal cry', 'XPO:0100642', 'abnormal gustatory system', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(135984, 'HP:0025429', 'Abnormal cry', 'XPO:0141745', 'abnormal creatinine homeostasis', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(135985, 'HP:0025429', 'Abnormal cry', 'XPO:0100610', 'abnormal appendage', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135986, 'HP:0025429', 'Abnormal cry', 'XPO:0100103', 'abnormal trunk', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135987, 'HP:0025429', 'Abnormal cry', 'XPO:0100484', 'abnormal cement gland primordium', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135988, 'HP:0025429', 'Abnormal cry', 'XPO:0100493', 'abnormal liver and biliary system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(135989, 'HP:0025429', 'Abnormal cry', 'XPO:0100784', 'abnormal left blastomere', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(135990, 'HP:0025429', 'Abnormal cry', 'XPO:0141787', 'abnormal hormone metabolic process', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(135991, 'HP:0025429', 'Abnormal cry', 'XPO:0100916', 'abnormal principal cavity', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(135992, 'HP:0025429', 'Abnormal cry', 'XPO:0101467', 'abnormal alkali secreting cell', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(135993, 'HP:0025429', 'Abnormal cry', 'XPO:0101333', 'abnormal barrier epithelial cell', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(135994, 'HP:0025429', 'Abnormal cry', 'XPO:0107270', 'abnormal proximal-distal axis', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135995, 'HP:0025429', 'Abnormal cry', 'XPO:0101263', 'abnormal blastocoel floor', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135996, 'HP:0025429', 'Abnormal cry', 'XPO:0100653', 'abnormal myoblast', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(135997, 'HP:0025429', 'Abnormal cry', 'XPO:0107276', 'abnormal dorsal region', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135998, 'HP:0025429', 'Abnormal cry', 'XPO:0100249', 'abnormal avascular GAG-rich matrix', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(135999, 'HP:0025429', 'Abnormal cry', 'XPO:0115505', 'dead whole organism', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(136000, 'HP:0025429', 'Abnormal cry', 'XPO:0100856', 'abnormal simple organ', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(136001, 'HP:0025429', 'Abnormal cry', 'XPO:0141795', 'abnormal glycosylation', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(136002, 'HP:0025429', 'Abnormal cry', 'XPO:0100009', 'abnormal multi-tissue structure', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(136003, 'HP:0025429', 'Abnormal cry', 'XPO:0101500', 'abnormal endodermal cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(136004, 'HP:0025429', 'Abnormal cry', 'XPO:0116091', 'abnormally increased variability of size of cell in endoderm', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(136005, 'HP:0025429', 'Abnormal cry', 'XPO:0101004', 'abnormal acid secreting cell', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(136006, 'HP:0025429', 'Abnormal cry', 'XPO:0100135', 'abnormal surface structure', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(136007, 'HP:0025429', 'Abnormal cry', 'XPO:0107288', 'abnormal larval alimentary system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(136008, 'HP:0025429', 'Abnormal cry', 'XPO:0100010', 'abnormal multicellular anatomical structure', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(136009, 'HP:0025429', 'Abnormal cry', 'XPO:0100062', 'abnormal anatomical space', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(136010, 'HP:0025429', 'Abnormal cry', 'XPO:0101575', 'abnormal vitelline membrane', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(136011, 'HP:0025429', 'Abnormal cry', 'XPO:0101141', 'abnormal Keller explant', 0.5294117647058824, 1.706362323152461, 0.9504568842024205, 'UPHENO:0002536', 'abnormal anatomical entity'),
(136012, 'HP:0025429', 'Abnormal cry', 'XPO:0100674', 'abnormal secondary oogonium', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(136013, 'HP:0025429', 'Abnormal cry', 'XPO:0131745', 'abnormal axis elongation', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(136014, 'HP:0025429', 'Abnormal cry', 'XPO:0115574', 'abnormal variability of size of hindlimb', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(136015, 'HP:0025429', 'Abnormal cry', 'XPO:0100186', 'abnormal uveal tract', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(136016, 'HP:0025429', 'Abnormal cry', 'XPO:0101587', 'abnormal hemangioblast', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(136017, 'HP:0025429', 'Abnormal cry', 'XPO:0100509', 'abnormal germ plasm', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(136018, 'HP:0025429', 'Abnormal cry', 'XPO:0100187', 'abnormal regenerating limb', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(136019, 'HP:0025429', 'Abnormal cry', 'XPO:0100028', 'abnormal anatomical cluster', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(136020, 'HP:0025429', 'Abnormal cry', 'XPO:0141266', 'abnormal surface breathing', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(136021, 'HP:0025429', 'Abnormal cry', 'XPO:0100239', 'abnormal acellular anatomical structure', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(136022, 'HP:0025429', 'Abnormal cry', 'XPO:0101553', 'abnormal dental epithelium', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(136023, 'HP:0025429', 'Abnormal cry', 'XPO:0100754', 'abnormal electrically active cell', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(136024, 'HP:0025429', 'Abnormal cry', 'XPO:0100108', 'abnormal cell part', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(136025, 'HP:0025429', 'Abnormal cry', 'XPO:0100974', 'abnormal cardiac mesoderm', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(136026, 'HP:0025429', 'Abnormal cry', 'XPO:0101389', 'abnormal wedge region', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(136027, 'HP:0025429', 'Abnormal cry', 'XPO:0100032', 'abnormal nervous system', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(136028, 'HP:0025429', 'Abnormal cry', 'XPO:0131729', 'abnormal regulation of growth rate', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(136029, 'HP:0025429', 'Abnormal cry', 'XPO:0131675', 'abnormal spindle microtubule', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(136030, 'HP:0025429', 'Abnormal cry', 'XPO:0100969', 'abnormal disaggregated/reaggregated ectoderm treated with activin', 0.5294117647058824, 1.706362323152461, 0.9504568842024205, 'UPHENO:0002536', 'abnormal anatomical entity'),
(136031, 'HP:0025429', 'Abnormal cry', 'XPO:0107260', 'abnormal anterior-posterior axis', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(136032, 'HP:0025429', 'Abnormal cry', 'XPO:0131730', 'abnormal regulation of protein folding', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(136033, 'HP:0025429', 'Abnormal cry', 'XPO:0141860', 'abnormal malate-aspartate shuttle', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(136034, 'HP:0025429', 'Abnormal cry', 'XPO:0116494', 'absent biological process', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(136035, 'HP:0025429', 'Abnormal cry', 'XPO:0100902', 'abnormal spermatocyte', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(136036, 'HP:0025429', 'Abnormal cry', 'XPO:0100588', 'abnormal unicellular gland', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(136037, 'HP:0025429', 'Abnormal cry', 'XPO:0100307', 'abnormal blastomere', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(136038, 'HP:0025429', 'Abnormal cry', 'XPO:0107269', 'abnormal right side', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(136039, 'HP:0025429', 'Abnormal cry', 'XPO:0100417', 'abnormal dense regular connective tissue', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(136040, 'HP:0025429', 'Abnormal cry', 'XPO:0100816', 'abnormal blastocoel anlage', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(136041, 'HP:0025429', 'Abnormal cry', 'XPO:0101168', 'abnormal circulating cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(136042, 'HP:0025429', 'Abnormal cry', 'XPO:0100854', 'abnormal spiracle', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(136043, 'HP:0025429', 'Abnormal cry', 'XPO:0101061', 'abnormal plasma membrane', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(136044, 'HP:0025429', 'Abnormal cry', 'XPO:0101326', 'abnormal cementoblast', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(136045, 'HP:0025429', 'Abnormal cry', 'XPO:0107261', 'abnormal dorsal-ventral axis', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(136046, 'HP:0025429', 'Abnormal cry', 'XPO:0100218', 'abnormal epithelial cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(136047, 'HP:0025429', 'Abnormal cry', 'XPO:0107266', 'abnormal dorsal side', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(136048, 'HP:0025429', 'Abnormal cry', 'XPO:0101368', 'abnormal regenerating eye', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(136049, 'HP:0025429', 'Abnormal cry', 'XPO:0100060', 'abnormal regenerating tissue', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(136050, 'HP:0025429', 'Abnormal cry', 'XPO:0100626', 'abnormal primordial germ cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(136051, 'HP:0025429', 'Abnormal cry', 'XPO:0100006', 'abnormal anatomical structure', 0.5625, 1.706362323152461, 0.9797085315405084, 'UPHENO:0002536', 'abnormal anatomical entity'),
(136052, 'HP:0025429', 'Abnormal cry', 'XPO:0100332', 'abnormal germinal granule', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(136053, 'HP:0025429', 'Abnormal cry', 'XPO:0128000', 'absent behavior', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(136054, 'HP:0025429', 'Abnormal cry', 'XPO:0100114', 'abnormal peripheral nervous system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(136055, 'HP:0025429', 'Abnormal cry', 'XPO:0101072', 'abnormal mitochondrial cloud', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(136056, 'HP:0025429', 'Abnormal cry', 'XPO:0100261', 'abnormal multilaminar epithelium', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(136057, 'HP:0025429', 'Abnormal cry', 'XPO:0101071', 'abnormal endoplasmic reticulum', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(136058, 'HP:0025429', 'Abnormal cry', 'XPO:0100867', 'abnormal apical mesenchyme', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(136059, 'HP:0025429', 'Abnormal cry', 'XPO:0100415', 'abnormal secretory epithelial cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(136060, 'HP:0025429', 'Abnormal cry', 'XPO:0100627', 'abnormal pharyngeal region', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(136061, 'HP:0025429', 'Abnormal cry', 'XPO:0141776', 'abnormal metabolic process', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(136062, 'HP:0025429', 'Abnormal cry', 'XPO:0126321', 'abnormally localised anatomical structure', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(136063, 'HP:0025429', 'Abnormal cry', 'XPO:0100295', 'abnormal extracellular matrix', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(136064, 'HP:0025429', 'Abnormal cry', 'XPO:0141770', 'abnormal urate homeostasis', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(136065, 'HP:0025429', 'Abnormal cry', 'XPO:0100392', 'abnormal cilium', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(136066, 'HP:0025429', 'Abnormal cry', 'XPO:0101638', 'abnormal anatomical structure morphology', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(136067, 'HP:0025429', 'Abnormal cry', 'XPO:0101573', 'abnormal peripheral vegetal yolk mass', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(136068, 'HP:0025429', 'Abnormal cry', 'XPO:0141499', 'abnormal tadpole', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(136069, 'HP:0025429', 'Abnormal cry', 'XPO:0101176', 'abnormal non-ciliated epithelial cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(136070, 'HP:0025429', 'Abnormal cry', 'XPO:0100202', 'abnormal embryo', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(136071, 'HP:0025429', 'Abnormal cry', 'XPO:0101463', 'abnormal right-ventral blastomere', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(136072, 'HP:0025429', 'Abnormal cry', 'XPO:0107264', 'abnormal anterior side', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(136073, 'HP:0025429', 'Abnormal cry', 'XPO:0101569', 'abnormal activin-induced ectoderm', 0.5294117647058824, 1.706362323152461, 0.9504568842024205, 'UPHENO:0002536', 'abnormal anatomical entity'),
(136074, 'HP:0025429', 'Abnormal cry', 'XPO:0100643', 'abnormal thoracic region', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(136075, 'HP:0025429', 'Abnormal cry', 'XPO:0131677', 'abnormal actin filament', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(136076, 'HP:0025429', 'Abnormal cry', 'XPO:0141892', 'abnormal inositol metabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(136077, 'HP:0025429', 'Abnormal cry', 'XPO:0141754', 'abnormal homeostatic process', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(136078, 'HP:0025429', 'Abnormal cry', 'XPO:0100599', 'abnormal adult immune system', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(136079, 'HP:0025429', 'Abnormal cry', 'XPO:0100531', 'abnormal proliferative region', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(136080, 'HP:0025429', 'Abnormal cry', 'XPO:0100296', 'abnormal tail region', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(136081, 'HP:0025429', 'Abnormal cry', 'XPO:0107339', 'abnormal yolk platelet', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(136082, 'HP:0025429', 'Abnormal cry', 'XPO:0141715', 'abnormal septum', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(136083, 'HP:0025429', 'Abnormal cry', 'XPO:0101424', 'abnormal coelomic epithelium', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(136084, 'HP:0025429', 'Abnormal cry', 'XPO:0100031', 'abnormal central nervous system', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(136085, 'HP:0025429', 'Abnormal cry', 'XPO:0100888', 'abnormal microtubule', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(136086, 'HP:0025429', 'Abnormal cry', 'XPO:0100468', 'abnormal muscular system', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(136087, 'HP:0025429', 'Abnormal cry', 'XPO:0100429', 'abnormal spermatid', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(136088, 'HP:0025429', 'Abnormal cry', 'XPO:0115473', 'abnormally delayed phase of Mullerian duct', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(136089, 'HP:0025429', 'Abnormal cry', 'XPO:0101212', 'abnormal glomeral mesenchyme', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(136090, 'HP:0025429', 'Abnormal cry', 'XPO:0131669', 'abnormal Roux spot', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(136091, 'HP:0025429', 'Abnormal cry', 'XPO:0100900', 'abnormal angioblast', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(136092, 'HP:0025429', 'Abnormal cry', 'XPO:0100612', 'abnormal unilaminar epithelium', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(136093, 'HP:0025429', 'Abnormal cry', 'XPO:0100273', 'abnormal visual system', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(136094, 'HP:0025429', 'Abnormal cry', 'XPO:0100394', 'abnormal marginal zone', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(136095, 'HP:0025429', 'Abnormal cry', 'XPO:0101347', 'abnormal hindlimb region', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(136096, 'HP:0025429', 'Abnormal cry', 'XPO:0101402', 'abnormal oropharyngeal papilla', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(136097, 'HP:0025429', 'Abnormal cry', 'XPO:0100242', 'abnormal right lymph heart', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(136098, 'HP:0025429', 'Abnormal cry', 'XPO:0101513', 'abnormal basal body', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(136099, 'HP:0025429', 'Abnormal cry', 'XPO:0101560', 'abnormal compound organ component', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(136100, 'HP:0025429', 'Abnormal cry', 'XPO:0101480', 'abnormal stage V oocyte', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(136101, 'HP:0025429', 'Abnormal cry', 'XPO:0100521', 'abnormal animal blastomere', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(136102, 'HP:0025429', 'Abnormal cry', 'XPO:0141841', 'abnormality of whole organism mass', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(136103, 'HP:0025429', 'Abnormal cry', 'XPO:0100070', 'abnormal anatomical system', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(136104, 'HP:0025429', 'Abnormal cry', 'XPO:0100750', 'abnormal regenerating fin', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(136105, 'HP:0025429', 'Abnormal cry', 'XPO:0101220', 'abnormal centriole', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(136106, 'HP:0025429', 'Abnormal cry', 'XPO:0100192', 'abnormal epithelium', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(136107, 'HP:0025429', 'Abnormal cry', 'XPO:0100796', 'abnormal pseudoblastema', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(136108, 'HP:0025429', 'Abnormal cry', 'XPO:0100026', 'abnormal germ cell', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(136109, 'HP:0025429', 'Abnormal cry', 'XPO:0100704', 'abnormal Merkel cell', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(136110, 'HP:0025429', 'Abnormal cry', 'XPO:0100258', 'abnormal organ part', 0.5294117647058824, 1.706362323152461, 0.9504568842024205, 'UPHENO:0002536', 'abnormal anatomical entity'),
(136111, 'HP:0025429', 'Abnormal cry', 'XPO:0100422', 'abnormal notochord', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(136112, 'HP:0025429', 'Abnormal cry', 'XPO:0100133', 'abnormal solid compound organ', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(136113, 'HP:0025429', 'Abnormal cry', 'XPO:0141784', 'abnormal cellular hormone metabolic process', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(136114, 'HP:0025429', 'Abnormal cry', 'XPO:0101110', 'abnormal cell-free extract', 0.5294117647058824, 1.706362323152461, 0.9504568842024205, 'UPHENO:0002536', 'abnormal anatomical entity'),
(136115, 'HP:0025429', 'Abnormal cry', 'XPO:0100823', 'abnormal blood', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(136116, 'HP:0025429', 'Abnormal cry', 'XPO:0100557', 'abnormal prime meridian', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(136117, 'HP:0025429', 'Abnormal cry', 'XPO:0100203', 'abnormal endocrine cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(136118, 'HP:0025429', 'Abnormal cry', 'XPO:0101098', 'abnormal mineralized extracellular matrix', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(136119, 'HP:0025429', 'Abnormal cry', 'XPO:0100251', 'abnormal proteinaceous extracellular matrix', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(136120, 'HP:0200111', 'Absent stapes head', 'XPO:0103707', 'increased pigmentation in the head', 0.40384615384615385, 4.5318002188002176, 1.3528303989641963, 'UPHENO:0087907', 'abnormal head morphology'),
(136121, 'HP:0200111', 'Absent stapes head', 'XPO:0100502', 'abnormal posterior semicircular canal', 0.4098360655737705, 7.26295268789559, 1.7252883683765938, 'UPHENO:0076730', 'abnormal ear morphology'),
(136122, 'HP:0200111', 'Absent stapes head', 'XPO:0102720', 'abnormal dermatocranium morphology', 0.4067796610169492, 4.5318002188002176, 1.3577349361344757, 'UPHENO:0087907', 'abnormal head morphology'),
(136123, 'HP:0200111', 'Absent stapes head', 'XPO:0101764', 'abnormal cranium morphology', 0.42105263157894735, 4.5318002188002176, 1.3813494879703256, 'UPHENO:0087907', 'abnormal head morphology'),
(136124, 'HP:0200111', 'Absent stapes head', 'XPO:0102637', 'abnormal middle ear morphology', 0.4918032786885246, 10.649807419403725, 2.288582575801915, 'UPHENO:0021692', 'abnormal middle ear morphology'),
(136125, 'HP:0200111', 'Absent stapes head', 'XPO:0100220', 'abnormal semicircular canal', 0.4166666666666667, 7.26295268789559, 1.7396063596754188, 'UPHENO:0076730', 'abnormal ear morphology'),
(136126, 'HP:0200111', 'Absent stapes head', 'XPO:0102776', 'abnormal fenestra subocularis morphology', 0.41379310344827586, 4.5318002188002176, 1.3693895270319973, 'UPHENO:0087907', 'abnormal head morphology'),
(136127, 'HP:0200111', 'Absent stapes head', 'XPO:0141835', 'edematous head', 0.4117647058823529, 4.5318002188002176, 1.3660290568695288, 'UPHENO:0087907', 'abnormal head morphology'),
(136128, 'HP:0200111', 'Absent stapes head', 'XPO:0100982', 'abnormal stapes', 0.44871794871794873, 10.7857850889227, 2.1999489449562306, 'HP:0004452', 'Abnormality of the middle ear ossicles'),
(136129, 'HP:0200111', 'Absent stapes head', 'XPO:0115526', 'abnormally incomplete structure of head', 0.42, 4.5318002188002176, 1.3796217205799897, 'UPHENO:0087907', 'abnormal head morphology'),
(136130, 'HP:0200111', 'Absent stapes head', 'XPO:0141298', 'abnormal intercanthal region morphology', 0.4117647058823529, 4.5318002188002176, 1.3660290568695288, 'UPHENO:0087907', 'abnormal head morphology'),
(136131, 'HP:0200111', 'Absent stapes head', 'XPO:0100420', 'abnormal choana', 0.42105263157894735, 4.5318002188002176, 1.3813494879703256, 'UPHENO:0087907', 'abnormal head morphology'),
(136132, 'HP:0200111', 'Absent stapes head', 'XPO:0103176', 'abnormal fenestra basicranialis morphology', 0.41379310344827586, 4.5318002188002176, 1.3693895270319973, 'UPHENO:0087907', 'abnormal head morphology'),
(136133, 'HP:0200111', 'Absent stapes head', 'XPO:0101473', 'abnormal pars media of the stapes', 0.4430379746835443, 10.7857850889227, 2.1859808739255437, 'HP:0004452', 'Abnormality of the middle ear ossicles'),
(136134, 'HP:0200111', 'Absent stapes head', 'XPO:0130309', 'increased size of the auditory tube', 0.4117647058823529, 10.24626555896271, 2.054032746642264, 'UPHENO:0088067', 'abnormal middle ear morphology'),
(136135, 'HP:0200111', 'Absent stapes head', 'XPO:0101301', 'abnormal utricle', 0.4430379746835443, 10.7857850889227, 2.1859808739255437, 'HP:0004452', 'Abnormality of the middle ear ossicles'),
(136136, 'HP:0200111', 'Absent stapes head', 'XPO:0130186', 'increased size of the middle ear', 0.4411764705882353, 10.649807419403725, 2.167589548262525, 'UPHENO:0021692', 'abnormal middle ear morphology'),
(136137, 'HP:0200111', 'Absent stapes head', 'XPO:0101076', 'abnormal footplate of the stapes', 0.4430379746835443, 10.7857850889227, 2.1859808739255437, 'HP:0004452', 'Abnormality of the middle ear ossicles'),
(136138, 'HP:0200111', 'Absent stapes head', 'XPO:0102092', 'abnormal ethmoid region morphology', 0.41379310344827586, 4.5318002188002176, 1.3693895270319973, 'UPHENO:0087907', 'abnormal head morphology'),
(136139, 'HP:0200111', 'Absent stapes head', 'XPO:0101028', 'abnormal sacculus', 0.4430379746835443, 10.7857850889227, 2.1859808739255437, 'HP:0004452', 'Abnormality of the middle ear ossicles'),
(136140, 'HP:0200111', 'Absent stapes head', 'XPO:0128831', 'decreased size of the auditory tube', 0.4117647058823529, 10.24626555896271, 2.054032746642264, 'UPHENO:0088067', 'abnormal middle ear morphology'),
(136141, 'HP:0200111', 'Absent stapes head', 'XPO:0100425', 'abnormal auditory ossicle', 0.47297297297297297, 10.7857850889227, 2.258624545902955, 'HP:0004452', 'Abnormality of the middle ear ossicles'),
(136142, 'HP:0200111', 'Absent stapes head', 'XPO:0141339', 'decreased pigmentation in the head', 0.40384615384615385, 4.5318002188002176, 1.3528303989641963, 'UPHENO:0087907', 'abnormal head morphology'),
(136143, 'HP:0200111', 'Absent stapes head', 'XPO:0101634', 'abnormal head morphology', 0.42857142857142855, 4.5318002188002176, 1.3936283915633758, 'UPHENO:0087907', 'abnormal head morphology'),
(136144, 'HP:0200111', 'Absent stapes head', 'XPO:0102259', 'abnormal pharyngeal region morphology', 0.4375, 4.5318002188002176, 1.4080705222839853, 'UPHENO:0087907', 'abnormal head morphology'),
(136145, 'HP:0200111', 'Absent stapes head', 'XPO:0100850', 'abnormal auditory tube', 0.4444444444444444, 9.964122330181212, 2.104399870132545, 'HP:0000370', 'Abnormality of the middle ear'),
(136146, 'HP:0200111', 'Absent stapes head', 'XPO:0141839', 'edematous pharyngeal region', 0.42, 4.5318002188002176, 1.3796217205799897, 'UPHENO:0087907', 'abnormal head morphology'),
(136147, 'HP:0200111', 'Absent stapes head', 'XPO:0101203', 'abnormal vestibule', 0.4166666666666667, 7.26295268789559, 1.7396063596754188, 'UPHENO:0076730', 'abnormal ear morphology'),
(136148, 'HP:0200111', 'Absent stapes head', 'XPO:0102734', 'abnormal craniofacial region morphology', 0.40384615384615385, 4.5318002188002176, 1.3528303989641963, 'UPHENO:0087907', 'abnormal head morphology'),
(136149, 'HP:0200111', 'Absent stapes head', 'XPO:0101179', 'abnormal pars interna of the stapes', 0.4430379746835443, 10.7857850889227, 2.1859808739255437, 'HP:0004452', 'Abnormality of the middle ear ossicles'),
(136150, 'HP:0200111', 'Absent stapes head', 'XPO:0102804', 'abnormal pharyngeal pouch morphology', 0.40384615384615385, 4.5318002188002176, 1.3528303989641963, 'UPHENO:0087907', 'abnormal head morphology'),
(136151, 'HP:0200111', 'Absent stapes head', 'XPO:0101383', 'abnormal anterior semicircular canal', 0.4098360655737705, 7.26295268789559, 1.7252883683765938, 'UPHENO:0076730', 'abnormal ear morphology'),
(136152, 'HP:0200111', 'Absent stapes head', 'XPO:0141085', 'abnormally necrotic auditory tube', 0.42424242424242425, 10.24626555896271, 2.0849221904344533, 'UPHENO:0088067', 'abnormal middle ear morphology'),
(136153, 'HP:0200111', 'Absent stapes head', 'XPO:0140335', 'abnormally necrotic pharyngeal region', 0.4117647058823529, 4.5318002188002176, 1.3660290568695288, 'UPHENO:0087907', 'abnormal head morphology'),
(136154, 'HP:0200111', 'Absent stapes head', 'XPO:0102665', 'abnormal suspensorium morphology', 0.4067796610169492, 4.5318002188002176, 1.3577349361344757, 'UPHENO:0087907', 'abnormal head morphology'),
(136155, 'HP:0200111', 'Absent stapes head', 'XPO:0100853', 'abnormal osseous labyrinth', 0.43103448275862066, 7.26295268789559, 1.769345374743837, 'UPHENO:0076730', 'abnormal ear morphology'),
(136156, 'HP:0200111', 'Absent stapes head', 'XPO:0102482', 'abnormal auditory tube morphology', 0.45901639344262296, 10.24626555896271, 2.1686871289170377, 'UPHENO:0088067', 'abnormal middle ear morphology'),
(136157, 'HP:0200111', 'Absent stapes head', 'XPO:0142059', 'abnormal nasal region morphology', 0.42, 4.5318002188002176, 1.3796217205799897, 'UPHENO:0087907', 'abnormal head morphology'),
(136158, 'HP:0200111', 'Absent stapes head', 'XPO:0103101', 'abnormal medial nasal prominence morphology', 0.40384615384615385, 4.5318002188002176, 1.3528303989641963, 'UPHENO:0087907', 'abnormal head morphology'),
(136159, 'HP:0200111', 'Absent stapes head', 'XPO:0101235', 'abnormal lagena', 0.423728813559322, 7.26295268789559, 1.754286842389091, 'UPHENO:0076730', 'abnormal ear morphology'),
(136160, 'HP:0200111', 'Absent stapes head', 'XPO:0101005', 'abnormal middle ear', 0.43636363636363634, 9.964122330181212, 2.085181203917296, 'HP:0000370', 'Abnormality of the middle ear'),
(136161, 'HP:0200111', 'Absent stapes head', 'XPO:0102005', 'abnormal splanchnocranium morphology', 0.4067796610169492, 4.5318002188002176, 1.3577349361344757, 'UPHENO:0087907', 'abnormal head morphology'),
(136162, 'HP:0200111', 'Absent stapes head', 'XPO:0101681', 'abnormal chondrocranium morphology', 0.4067796610169492, 4.5318002188002176, 1.3577349361344757, 'UPHENO:0087907', 'abnormal head morphology'),
(136163, 'HP:0200111', 'Absent stapes head', 'XPO:0102224', 'abnormal auditory apparatus morphology', 0.4098360655737705, 7.26295268789559, 1.7252883683765938, 'UPHENO:0076730', 'abnormal ear morphology'),
(136164, 'HP:0200111', 'Absent stapes head', 'XPO:0128707', 'decreased size of the middle ear', 0.4411764705882353, 10.649807419403725, 2.167589548262525, 'UPHENO:0021692', 'abnormal middle ear morphology'),
(136165, 'HP:0200111', 'Absent stapes head', 'XPO:0102538', 'abnormal lateral nasal prominence morphology', 0.40384615384615385, 4.5318002188002176, 1.3528303989641963, 'UPHENO:0087907', 'abnormal head morphology'),
(136166, 'HP:0200111', 'Absent stapes head', 'XPO:0100224', 'abnormal lateral semicircular canal', 0.4098360655737705, 7.26295268789559, 1.7252883683765938, 'UPHENO:0076730', 'abnormal ear morphology'),
(136167, 'HP:0200111', 'Absent stapes head', 'XPO:0140080', 'abnormally necrotic middle ear', 0.45454545454545453, 10.649807419403725, 2.2001867089577694, 'UPHENO:0021692', 'abnormal middle ear morphology'),
(136168, 'HP:0200111', 'Absent stapes head', 'XPO:0101527', 'abnormal pars externa of the stapes', 0.4430379746835443, 10.7857850889227, 2.1859808739255437, 'HP:0004452', 'Abnormality of the middle ear ossicles'),
(136169, 'HP:0200111', 'Absent stapes head', 'XPO:0126806', 'abnormally localised auditory tube', 0.4032258064516129, 9.964122330181212, 2.004442880745132, 'HP:0000370', 'Abnormality of the middle ear'),
(136170, 'HP:0030326', 'Abnormal macrophage count', 'XPO:0125284', 'absent thymocyte', 0.43373493975903615, 8.086636373141483, 1.8728205306856691, 'UPHENO:0085984', 'abnormal number of anatomical enitites of type leukocyte'),
(136171, 'HP:0009875', 'Triangular shaped distal phalanges of the hand', 'XPO:0140219', 'abnormally necrotic forelimb digit', 0.40869565217391307, 7.492661022682715, 1.7499194219115835, 'HP:0001167', 'Abnormal finger morphology'),
(136172, 'HP:0009875', 'Triangular shaped distal phalanges of the hand', 'XPO:0103467', 'bifurcated forelimb digit 4', 0.4180327868852459, 8.968875860151847, 1.9363068380417097, 'UPHENO:0082301', 'shape anatomical entity in pectoral complex'),
(136173, 'HP:0009875', 'Triangular shaped distal phalanges of the hand', 'XPO:0103466', 'bifurcated forelimb digit 3', 0.4180327868852459, 8.968875860151847, 1.9363068380417097, 'UPHENO:0082301', 'shape anatomical entity in pectoral complex'),
(136174, 'HP:0009875', 'Triangular shaped distal phalanges of the hand', 'XPO:0115789', 'duplicated forelimb digit 5 in regenerating forelimb', 0.4351145038167939, 7.774297771301195, 1.839214429391996, 'HP:0005918', 'Abnormal finger phalanx morphology'),
(136175, 'HP:0009875', 'Triangular shaped distal phalanges of the hand', 'XPO:0103634', 'abnormally increased number of forelimb digit', 0.475, 7.774297771301195, 1.9216637170348165, 'HP:0005918', 'Abnormal finger phalanx morphology'),
(136176, 'HP:0009875', 'Triangular shaped distal phalanges of the hand', 'XPO:0141556', 'abnormal forelimb digit morphology in the regenerating forelimb', 0.415929203539823, 7.492661022682715, 1.7653375120804229, 'HP:0001167', 'Abnormal finger morphology'),
(136177, 'HP:0009875', 'Triangular shaped distal phalanges of the hand', 'XPO:0102746', 'abnormal forelimb digit 2 morphology', 0.43119266055045874, 7.492661022682715, 1.7974371869340195, 'HP:0001167', 'Abnormal finger morphology'),
(136178, 'HP:0009875', 'Triangular shaped distal phalanges of the hand', 'XPO:0115786', 'duplicated forelimb digit 2 in regenerating forelimb', 0.4351145038167939, 7.774297771301195, 1.839214429391996, 'HP:0005918', 'Abnormal finger phalanx morphology'),
(136179, 'HP:0009875', 'Triangular shaped distal phalanges of the hand', 'XPO:0103609', 'abnormally increased number of forelimb digit in the regenerating forelimb', 0.4523809523809524, 7.774297771301195, 1.875351761636827, 'HP:0005918', 'Abnormal finger phalanx morphology'),
(136180, 'HP:0009875', 'Triangular shaped distal phalanges of the hand', 'XPO:0102787', 'abnormal forelimb digit 5 morphology', 0.43119266055045874, 7.492661022682715, 1.7974371869340195, 'HP:0001167', 'Abnormal finger morphology'),
(136181, 'HP:0009875', 'Triangular shaped distal phalanges of the hand', 'XPO:0115788', 'duplicated forelimb digit 4 in regenerating forelimb', 0.4351145038167939, 7.774297771301195, 1.839214429391996, 'HP:0005918', 'Abnormal finger phalanx morphology'),
(136182, 'HP:0009875', 'Triangular shaped distal phalanges of the hand', 'XPO:0102214', 'abnormal forelimb digit morphology', 0.4392523364485981, 7.492661022682715, 1.8141578929163595, 'HP:0001167', 'Abnormal finger morphology'),
(136183, 'HP:0009875', 'Triangular shaped distal phalanges of the hand', 'XPO:0103755', 'increased size of the forelimb digit', 0.4017094017094017, 7.492661022682715, 1.734898376457027, 'HP:0001167', 'Abnormal finger morphology'),
(136184, 'HP:0009875', 'Triangular shaped distal phalanges of the hand', 'XPO:0103468', 'bifurcated forelimb digit 5', 0.4180327868852459, 8.968875860151847, 1.9363068380417097, 'UPHENO:0082301', 'shape anatomical entity in pectoral complex'),
(136185, 'HP:0009875', 'Triangular shaped distal phalanges of the hand', 'XPO:0102598', 'abnormal forelimb digit 3 morphology', 0.43119266055045874, 7.492661022682715, 1.7974371869340195, 'HP:0001167', 'Abnormal finger morphology'),
(136186, 'HP:0009875', 'Triangular shaped distal phalanges of the hand', 'XPO:0102529', 'abnormal forelimb digit 4 morphology', 0.43119266055045874, 7.492661022682715, 1.7974371869340195, 'HP:0001167', 'Abnormal finger morphology'),
(136187, 'HP:0009875', 'Triangular shaped distal phalanges of the hand', 'XPO:0115787', 'duplicated forelimb digit 3 in regenerating forelimb', 0.4351145038167939, 7.774297771301195, 1.839214429391996, 'HP:0005918', 'Abnormal finger phalanx morphology'),
(136188, 'HP:0009875', 'Triangular shaped distal phalanges of the hand', 'XPO:0103465', 'bifurcated forelimb digit 2', 0.4180327868852459, 8.968875860151847, 1.9363068380417097, 'UPHENO:0082301', 'shape anatomical entity in pectoral complex'),
(136189, 'HP:0009875', 'Triangular shaped distal phalanges of the hand', 'XPO:0133358', 'fused forelimb digits', 0.4051724137931034, 7.492661022682715, 1.7423603393941962, 'HP:0001167', 'Abnormal finger morphology'),
(136190, 'HP:0009027', 'Foot dorsiflexor weakness', 'XPO:0100768', 'abnormal pectoral girdle', 0.4117647058823529, 9.463856994035337, 1.9740522515023784, 'UPHENO:0002647', 'abnormal musculature of limb'),
(136191, 'HP:0034157', 'Anti-beta-2-Glycoprotein I IgM antibody positivity', 'XPO:0101029', 'abnormal right spleen primordium', 0.40625, 5.64885357140806, 1.5148751642906173, 'HP:0002715', 'Abnormality of the immune system'),
(136192, 'HP:0034157', 'Anti-beta-2-Glycoprotein I IgM antibody positivity', 'XPO:0100449', 'abnormal lymphocyte', 0.40625, 5.64885357140806, 1.5148751642906173, 'HP:0002715', 'Abnormality of the immune system'),
(136193, 'HP:0034157', 'Anti-beta-2-Glycoprotein I IgM antibody positivity', 'XPO:0101221', 'abnormal larval immune system', 0.4482758620689655, 5.64885357140806, 1.5913028324062968, 'HP:0002715', 'Abnormality of the immune system'),
(136194, 'HP:0034157', 'Anti-beta-2-Glycoprotein I IgM antibody positivity', 'XPO:0100599', 'abnormal adult immune system', 0.4482758620689655, 5.64885357140806, 1.5913028324062968, 'HP:0002715', 'Abnormality of the immune system'),
(136195, 'HP:0034157', 'Anti-beta-2-Glycoprotein I IgM antibody positivity', 'XPO:0100745', 'abnormal anterior lymph sac', 0.41935483870967744, 5.64885357140806, 1.5391147060347428, 'HP:0002715', 'Abnormality of the immune system'),
(136196, 'HP:0034157', 'Anti-beta-2-Glycoprotein I IgM antibody positivity', 'XPO:0101451', 'abnormal dorsal lymph space', 0.43333333333333335, 5.64885357140806, 1.5645563421015427, 'HP:0002715', 'Abnormality of the immune system'),
(136197, 'HP:0034157', 'Anti-beta-2-Glycoprotein I IgM antibody positivity', 'XPO:0100232', 'abnormal lymphatic system', 0.4642857142857143, 5.64885357140806, 1.6194696710023933, 'HP:0002715', 'Abnormality of the immune system'),
(136198, 'HP:0034157', 'Anti-beta-2-Glycoprotein I IgM antibody positivity', 'XPO:0141497', 'abnormal lymphoblast', 0.40625, 5.64885357140806, 1.5148751642906173, 'HP:0002715', 'Abnormality of the immune system'),
(136199, 'HP:0034157', 'Anti-beta-2-Glycoprotein I IgM antibody positivity', 'XPO:0100581', 'abnormal immune system', 0.4642857142857143, 5.64885357140806, 1.6194696710023933, 'HP:0002715', 'Abnormality of the immune system'),
(136200, 'HP:0012020', 'Right aortic arch', 'XPO:0129510', 'increased size of the blood vessel', 0.41379310344827586, 6.974839882869777, 1.6988645152534954, 'UPHENO:0087186', 'abnormal blood vessel morphology'),
(136201, 'HP:0012020', 'Right aortic arch', 'XPO:0102565', 'abnormal branchial vein morphology', 0.43103448275862066, 7.803720102857406, 1.8340317494875034, 'HP:0033353', 'Abnormal blood vessel morphology'),
(136202, 'HP:0012020', 'Right aortic arch', 'XPO:0103091', 'abnormal arteria iliaca communis morphology', 0.40298507462686567, 8.750570396338642, 1.877857626178345, 'HP:0011004', 'Abnormal systemic arterial morphology'),
(136203, 'HP:0012020', 'Right aortic arch', 'XPO:0129184', 'decreased size of the arteria mesenterica posterior', 0.4189189189189189, 9.604719529875187, 2.0058910045101506, 'UPHENO:0076809', 'abnormal aorta morphology'),
(136204, 'HP:0012020', 'Right aortic arch', 'XPO:0101916', 'abnormal tail vasculature morphology', 0.4067796610169492, 6.974839882869777, 1.6844058309093048, 'UPHENO:0087186', 'abnormal blood vessel morphology'),
(136205, 'HP:0012020', 'Right aortic arch', 'XPO:0140133', 'abnormally necrotic dorsal aorta', 0.4246575342465753, 9.604719529875187, 2.0195832522297077, 'UPHENO:0076809', 'abnormal aorta morphology'),
(136206, 'HP:0012020', 'Right aortic arch', 'XPO:0101956', 'abnormal intersomitic vessel morphology', 0.42105263157894735, 6.974839882869777, 1.7137020416408788, 'UPHENO:0087186', 'abnormal blood vessel morphology'),
(136207, 'HP:0012020', 'Right aortic arch', 'XPO:0128092', 'decreased size of the paired dorsal aorta', 0.44285714285714284, 9.604719529875187, 2.0624060339672994, 'UPHENO:0076809', 'abnormal aorta morphology'),
(136208, 'HP:0012020', 'Right aortic arch', 'XPO:0129844', 'increased size of the dorsal aorta', 0.41333333333333333, 9.604719529875187, 1.9924735227889672, 'UPHENO:0076809', 'abnormal aorta morphology'),
(136209, 'HP:0012020', 'Right aortic arch', 'XPO:0141554', 'abnormal blood vessel morphology in the regenerating hindlimb', 0.42105263157894735, 6.974839882869777, 1.7137020416408788, 'UPHENO:0087186', 'abnormal blood vessel morphology'),
(136210, 'HP:0012020', 'Right aortic arch', 'XPO:0128093', 'decreased size of the aorta', 0.4626865671641791, 9.604719529875187, 2.1080736960203024, 'UPHENO:0076809', 'abnormal aorta morphology'),
(136211, 'HP:0012020', 'Right aortic arch', 'XPO:0102613', 'abnormal dorsal longitudinal anastomosing vessel morphology', 0.4528301886792453, 6.974839882869777, 1.7771938724200707, 'UPHENO:0087186', 'abnormal blood vessel morphology'),
(136212, 'HP:0012020', 'Right aortic arch', 'XPO:0102154', 'abnormal subinterstitial vein morphology', 0.43103448275862066, 7.803720102857406, 1.8340317494875034, 'HP:0033353', 'Abnormal blood vessel morphology'),
(136213, 'HP:0012020', 'Right aortic arch', 'XPO:0139730', 'abnormally necrotic vein', 0.4032258064516129, 7.803720102857406, 1.7738831223610367, 'HP:0033353', 'Abnormal blood vessel morphology'),
(136214, 'HP:0012020', 'Right aortic arch', 'XPO:0102619', 'abnormal larval aorta morphology', 0.42105263157894735, 6.974839882869777, 1.7137020416408788, 'UPHENO:0087186', 'abnormal blood vessel morphology'),
(136215, 'HP:0012020', 'Right aortic arch', 'XPO:0101675', 'abnormal vein morphology', 0.44642857142857145, 7.803720102857406, 1.86649500865849, 'HP:0033353', 'Abnormal blood vessel morphology'),
(136216, 'HP:0012020', 'Right aortic arch', 'XPO:0101780', 'abnormal arteria mesenterica posterior morphology', 0.47692307692307695, 9.604719529875187, 2.1402598886983895, 'UPHENO:0076809', 'abnormal aorta morphology'),
(136217, 'HP:0012020', 'Right aortic arch', 'XPO:0102875', 'abnormal vertebral artery morphology', 0.42105263157894735, 6.974839882869777, 1.7137020416408788, 'UPHENO:0087186', 'abnormal blood vessel morphology'),
(136218, 'HP:0012020', 'Right aortic arch', 'XPO:0128147', 'decreased size of the ventral aorta', 0.41333333333333333, 9.604719529875187, 1.9924735227889672, 'UPHENO:0076809', 'abnormal aorta morphology'),
(136219, 'HP:0012020', 'Right aortic arch', 'XPO:0102424', 'abnormal capillary morphology', 0.44642857142857145, 7.803720102857406, 1.86649500865849, 'HP:0033353', 'Abnormal blood vessel morphology'),
(136220, 'HP:0012020', 'Right aortic arch', 'XPO:0102838', 'abnormal ischiadic vein morphology', 0.43103448275862066, 7.803720102857406, 1.8340317494875034, 'HP:0033353', 'Abnormal blood vessel morphology'),
(136221, 'HP:0012020', 'Right aortic arch', 'XPO:0103189', 'abnormal Jacobsons vein morphology', 0.43103448275862066, 7.803720102857406, 1.8340317494875034, 'HP:0033353', 'Abnormal blood vessel morphology'),
(136222, 'HP:0012020', 'Right aortic arch', 'XPO:0129572', 'increased size of the paired dorsal aorta', 0.44285714285714284, 9.604719529875187, 2.0624060339672994, 'UPHENO:0076809', 'abnormal aorta morphology'),
(136223, 'HP:0012020', 'Right aortic arch', 'XPO:0130660', 'increased size of the arteria mesenterica posterior', 0.4189189189189189, 9.604719529875187, 2.0058910045101506, 'UPHENO:0076809', 'abnormal aorta morphology'),
(136224, 'HP:0012020', 'Right aortic arch', 'XPO:0130819', 'increased size of the caudal artery', 0.4246575342465753, 9.604719529875187, 2.0195832522297077, 'UPHENO:0076809', 'abnormal aorta morphology'),
(136225, 'HP:0012020', 'Right aortic arch', 'XPO:0139828', 'abnormally necrotic paired dorsal aorta', 0.45588235294117646, 9.604719529875187, 2.09251574393589, 'UPHENO:0076809', 'abnormal aorta morphology'),
(136226, 'HP:0012020', 'Right aortic arch', 'XPO:0129627', 'increased size of the ventral aorta', 0.41333333333333333, 9.604719529875187, 1.9924735227889672, 'UPHENO:0076809', 'abnormal aorta morphology'),
(136227, 'HP:0012020', 'Right aortic arch', 'XPO:0101154', 'abnormal external carotid artery', 0.421875, 8.750570396338642, 1.921365890702592, 'HP:0011004', 'Abnormal systemic arterial morphology'),
(136228, 'HP:0012020', 'Right aortic arch', 'XPO:0101840', 'abnormal ventral aorta morphology', 0.47692307692307695, 9.604719529875187, 2.1402598886983895, 'UPHENO:0076809', 'abnormal aorta morphology'),
(136229, 'HP:0012020', 'Right aortic arch', 'XPO:0102412', 'abnormal vascular plexus morphology', 0.4444444444444444, 6.974839882869777, 1.7606614770679263, 'UPHENO:0087186', 'abnormal blood vessel morphology'),
(136230, 'HP:0012020', 'Right aortic arch', 'XPO:0101712', 'abnormal aorta morphology', 0.5344827586206896, 9.604719529875187, 2.2657354192636223, 'UPHENO:0076809', 'abnormal aorta morphology'),
(136231, 'HP:0012020', 'Right aortic arch', 'XPO:0141134', 'abnormally necrotic caudal artery', 0.43661971830985913, 9.604719529875187, 2.047830543667934, 'UPHENO:0076809', 'abnormal aorta morphology'),
(136232, 'HP:0012020', 'Right aortic arch', 'XPO:0140152', 'abnormally necrotic capillary', 0.4032258064516129, 7.803720102857406, 1.7738831223610367, 'HP:0033353', 'Abnormal blood vessel morphology'),
(136233, 'HP:0012020', 'Right aortic arch', 'XPO:0102612', 'abnormal dorsal longitudinal anastomosing vessel - left branch morphology', 0.43636363636363634, 6.974839882869777, 1.744582040015079, 'UPHENO:0087186', 'abnormal blood vessel morphology'),
(136234, 'HP:0012020', 'Right aortic arch', 'XPO:0103063', 'abnormal ischiadic artery morphology', 0.42105263157894735, 6.974839882869777, 1.7137020416408788, 'UPHENO:0087186', 'abnormal blood vessel morphology'),
(136235, 'HP:0012020', 'Right aortic arch', 'XPO:0140850', 'abnormally necrotic arteria mesenterica posterior', 0.4305555555555556, 9.604719529875187, 2.0335597736827666, 'UPHENO:0076809', 'abnormal aorta morphology'),
(136236, 'HP:0012020', 'Right aortic arch', 'XPO:0140809', 'abnormally necrotic truncus arteriosus', 0.4067796610169492, 6.974839882869777, 1.6844058309093048, 'UPHENO:0087186', 'abnormal blood vessel morphology'),
(136237, 'HP:0012020', 'Right aortic arch', 'XPO:0102421', 'abnormal occipitovertebral artery morphology', 0.42105263157894735, 6.974839882869777, 1.7137020416408788, 'UPHENO:0087186', 'abnormal blood vessel morphology'),
(136238, 'HP:0012020', 'Right aortic arch', 'XPO:0128030', 'decreased size of the blood vessel', 0.41379310344827586, 6.974839882869777, 1.6988645152534954, 'UPHENO:0087186', 'abnormal blood vessel morphology'),
(136239, 'HP:0012020', 'Right aortic arch', 'XPO:0101708', 'abnormal artery morphology', 0.43636363636363634, 6.974839882869777, 1.744582040015079, 'UPHENO:0087186', 'abnormal blood vessel morphology'),
(136240, 'HP:0012020', 'Right aortic arch', 'XPO:0101769', 'abnormal cardinal vein morphology', 0.4166666666666667, 7.803720102857406, 1.8032054910234865, 'HP:0033353', 'Abnormal blood vessel morphology'),
(136241, 'HP:0012020', 'Right aortic arch', 'XPO:0102329', 'abnormal caudal artery morphology', 0.484375, 9.604719529875187, 2.156915858878898, 'UPHENO:0076809', 'abnormal aorta morphology'),
(136242, 'HP:0012020', 'Right aortic arch', 'XPO:0139802', 'abnormally necrotic ventral aorta', 0.4246575342465753, 9.604719529875187, 2.0195832522297077, 'UPHENO:0076809', 'abnormal aorta morphology'),
(136243, 'HP:0012020', 'Right aortic arch', 'XPO:0140595', 'abnormally necrotic dorsal longitudinal anastomosing vessel', 0.4067796610169492, 6.974839882869777, 1.6844058309093048, 'UPHENO:0087186', 'abnormal blood vessel morphology'),
(136244, 'HP:0012020', 'Right aortic arch', 'XPO:0101686', 'abnormal blood vessel morphology', 0.47058823529411764, 6.974839882869777, 1.8117057133924146, 'UPHENO:0087186', 'abnormal blood vessel morphology'),
(136245, 'HP:0012020', 'Right aortic arch', 'XPO:0129573', 'increased size of the aorta', 0.4626865671641791, 9.604719529875187, 2.1080736960203024, 'UPHENO:0076809', 'abnormal aorta morphology'),
(136246, 'HP:0012020', 'Right aortic arch', 'XPO:0103215', 'abnormal truncus arteriosus morphology', 0.4528301886792453, 6.974839882869777, 1.7771938724200707, 'UPHENO:0087186', 'abnormal blood vessel morphology'),
(136247, 'HP:0012020', 'Right aortic arch', 'XPO:0103217', 'abnormal dorsal longitudinal anastomosing vessel - right branch morphology', 0.43636363636363634, 6.974839882869777, 1.744582040015079, 'UPHENO:0087186', 'abnormal blood vessel morphology'),
(136248, 'HP:0012020', 'Right aortic arch', 'XPO:0101774', 'abnormal paired dorsal aorta morphology', 0.5166666666666667, 9.604719529875187, 2.2276531201623038, 'UPHENO:0076809', 'abnormal aorta morphology'),
(136249, 'HP:0012020', 'Right aortic arch', 'XPO:0102683', 'abnormal intersomitic vein morphology', 0.4067796610169492, 6.974839882869777, 1.6844058309093048, 'UPHENO:0087186', 'abnormal blood vessel morphology'),
(136250, 'HP:0012020', 'Right aortic arch', 'XPO:0129344', 'decreased size of the caudal artery', 0.4246575342465753, 9.604719529875187, 2.0195832522297077, 'UPHENO:0076809', 'abnormal aorta morphology'),
(136251, 'HP:0012020', 'Right aortic arch', 'XPO:0101711', 'abnormal dorsal aorta morphology', 0.47692307692307695, 9.604719529875187, 2.1402598886983895, 'UPHENO:0076809', 'abnormal aorta morphology'),
(136252, 'HP:0012020', 'Right aortic arch', 'XPO:0139723', 'abnormally necrotic blood vessel', 0.42857142857142855, 6.974839882869777, 1.7289352482549702, 'UPHENO:0087186', 'abnormal blood vessel morphology'),
(136253, 'HP:0012020', 'Right aortic arch', 'XPO:0139803', 'abnormally necrotic aorta', 0.47692307692307695, 9.604719529875187, 2.1402598886983895, 'UPHENO:0076809', 'abnormal aorta morphology'),
(136254, 'HP:0012020', 'Right aortic arch', 'XPO:0128364', 'decreased size of the dorsal aorta', 0.41333333333333333, 9.604719529875187, 1.9924735227889672, 'UPHENO:0076809', 'abnormal aorta morphology'),
(136255, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0101448', 'abnormal myelin accumulating cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(136256, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0102307', 'abnormal dorsal vegetal hemisphere blastomere morphology', 0.4090909090909091, 5.43643956286526, 1.491307481034791, 'HP:0025461', 'Abnormal cell morphology'),
(136257, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0103099', 'abnormal alkali secreting cell morphology', 0.5454545454545454, 5.43643956286526, 1.7220135512398786, 'HP:0025461', 'Abnormal cell morphology'),
(136258, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0103122', 'abnormal ectodermal cell morphology', 0.4186046511627907, 5.43643956286526, 1.5085486027240909, 'HP:0025461', 'Abnormal cell morphology'),
(136259, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0115704', 'abnormally defasciculated motor neuron', 0.4186046511627907, 5.43643956286526, 1.5085486027240909, 'HP:0025461', 'Abnormal cell morphology'),
(136260, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0130883', 'increased size of the hemangioblast', 0.40816326530612246, 5.574066539846944, 1.5083531416540121, 'UPHENO:0004459', 'abnormal hematopoietic system'),
(136261, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0115617', 'abnormally posterioralized primordial germ cell', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(136262, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0101373', 'abnormal oxygen accumulating cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(136263, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0103104', 'abnormal zygote cortex morphology', 0.45714285714285713, 3.6715585125471644, 1.2955411026258445, 'UPHENO:0086172', 'abnormal cell'),
(136264, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0101311', 'abnormal bottle cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(136265, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0107371', 'abnormal migrating myoblast morphology', 0.5142857142857142, 5.43643956286526, 1.6720894724144628, 'HP:0025461', 'Abnormal cell morphology'),
(136266, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0102998', 'abnormal morula cell morphology', 0.4864864864864865, 5.43643956286526, 1.626270082715184, 'HP:0025461', 'Abnormal cell morphology'),
(136267, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0101302', 'abnormal subcortical cytoplasm', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(136268, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0101132', 'abnormal apoptotic cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(136269, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0101828', 'abnormal neuron morphology', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(136270, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0101636', 'abnormal cell morphology', 0.5806451612903226, 5.43643956286526, 1.776694213089295, 'HP:0025461', 'Abnormal cell morphology'),
(136271, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0102901', 'abnormal mesodermal cell morphology', 0.4186046511627907, 5.43643956286526, 1.5085486027240909, 'HP:0025461', 'Abnormal cell morphology'),
(136272, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0102446', 'abnormal natural killer cell morphology', 0.4186046511627907, 5.43643956286526, 1.5085486027240909, 'HP:0025461', 'Abnormal cell morphology'),
(136273, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0102706', 'abnormal germinal vesicle morphology', 0.42105263157894735, 3.6715585125471644, 1.2433500608051093, 'UPHENO:0086172', 'abnormal cell'),
(136274, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0102336', 'abnormal Merkel cell morphology', 0.5454545454545454, 5.43643956286526, 1.7220135512398786, 'HP:0025461', 'Abnormal cell morphology'),
(136275, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0101405', 'abnormal ring structure', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(136276, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0100308', 'abnormal early embryonic cell', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(136277, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0102943', 'abnormal bottle cell morphology', 0.46153846153846156, 5.43643956286526, 1.5840220806831131, 'HP:0025461', 'Abnormal cell morphology'),
(136278, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0131666', 'abnormal adherens junction', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(136279, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0129409', 'decreased size of the hemangioblast', 0.40816326530612246, 5.574066539846944, 1.5083531416540121, 'UPHENO:0004459', 'abnormal hematopoietic system'),
(136280, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0102024', 'abnormal cilium morphology', 0.45714285714285713, 3.6715585125471644, 1.2955411026258445, 'UPHENO:0086172', 'abnormal cell'),
(136281, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0101547', 'abnormal lampbrush chromosome', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(136282, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0140709', 'abnormally necrotic acid secreting cell', 0.4864864864864865, 5.43643956286526, 1.626270082715184, 'HP:0025461', 'Abnormal cell morphology'),
(136283, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0140059', 'abnormally necrotic epithelial cell', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(136284, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0102764', 'abnormal apoptotic cell morphology', 0.5454545454545454, 5.43643956286526, 1.7220135512398786, 'HP:0025461', 'Abnormal cell morphology'),
(136285, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0100715', 'abnormal ciliated cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(136286, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0100802', 'abnormal exocrine cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(136287, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0100902', 'abnormal spermatocyte', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(136288, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0101638', 'abnormal anatomical structure morphology', 0.42857142857142855, 2.7446671847279203, 1.0845671654222093, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(136289, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0140919', 'abnormally necrotic cementoblast', 0.4864864864864865, 5.43643956286526, 1.626270082715184, 'HP:0025461', 'Abnormal cell morphology'),
(136290, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0102636', 'abnormal acid secreting cell morphology', 0.5454545454545454, 5.43643956286526, 1.7220135512398786, 'HP:0025461', 'Abnormal cell morphology'),
(136291, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0139951', 'abnormally necrotic lymphocyte', 0.4186046511627907, 5.43643956286526, 1.5085486027240909, 'HP:0025461', 'Abnormal cell morphology'),
(136292, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0102860', 'abnormal mesenchymal stem cell morphology', 0.5142857142857142, 5.43643956286526, 1.6720894724144628, 'HP:0025461', 'Abnormal cell morphology'),
(136293, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0101969', 'abnormal zygote morphology', 0.5454545454545454, 5.43643956286526, 1.7220135512398786, 'HP:0025461', 'Abnormal cell morphology'),
(136294, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0140393', 'abnormally necrotic spermatocyte', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(136295, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0140767', 'abnormally necrotic stage IV oocyte', 0.4186046511627907, 5.43643956286526, 1.5085486027240909, 'HP:0025461', 'Abnormal cell morphology'),
(136296, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0100791', 'abnormal multiciliated cell precursor', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(136297, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0100574', 'abnormal gastrula cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(136298, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0139902', 'abnormally necrotic endocrine cell', 0.4090909090909091, 5.43643956286526, 1.491307481034791, 'HP:0025461', 'Abnormal cell morphology'),
(136299, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0141299', 'abnormal actin filament morphology', 0.45714285714285713, 3.6715585125471644, 1.2955411026258445, 'UPHENO:0086172', 'abnormal cell'),
(136300, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0103130', 'abnormal stage II oocyte morphology', 0.4864864864864865, 5.43643956286526, 1.626270082715184, 'HP:0025461', 'Abnormal cell morphology'),
(136301, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0100907', 'abnormal cytoplasm', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(136302, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0100989', 'abnormal right blastomere', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(136303, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0133436', 'abnormal cilium morphology in the multiciliated cell', 0.43243243243243246, 3.6715585125471644, 1.2600400701560144, 'UPHENO:0086172', 'abnormal cell'),
(136304, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0102532', 'abnormal angioblast morphology', 0.43902439024390244, 5.43643956286526, 1.5449043867452603, 'HP:0025461', 'Abnormal cell morphology'),
(136305, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0101378', 'abnormal blastomere D1', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(136306, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0101237', 'abnormal mucus secreting cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(136307, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0102739', 'abnormal erythroid cell morphology', 0.5405405405405406, 5.574066539846944, 1.735802102907416, 'HP:0001871', 'Abnormality of blood and blood-forming tissues'),
(136308, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0141065', 'abnormally necrotic paracrine cell', 0.4864864864864865, 5.43643956286526, 1.626270082715184, 'HP:0025461', 'Abnormal cell morphology'),
(136309, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0102703', 'abnormal endoplasmic reticulum morphology', 0.47058823529411764, 3.6715585125471644, 1.3144551118994765, 'UPHENO:0086172', 'abnormal cell'),
(136310, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0100176', 'abnormal stage VI oocyte', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(136311, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0102423', 'abnormal multiciliated cell precursor morphology', 0.5454545454545454, 5.43643956286526, 1.7220135512398786, 'HP:0025461', 'Abnormal cell morphology'),
(136312, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0140781', 'abnormally necrotic stage I oocyte', 0.4186046511627907, 5.43643956286526, 1.5085486027240909, 'HP:0025461', 'Abnormal cell morphology'),
(136313, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0140899', 'abnormally necrotic mucus secreting cell', 0.4864864864864865, 5.43643956286526, 1.626270082715184, 'HP:0025461', 'Abnormal cell morphology'),
(136314, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0102135', 'abnormal blastomere D2 morphology', 0.46153846153846156, 5.43643956286526, 1.5840220806831131, 'HP:0025461', 'Abnormal cell morphology'),
(136315, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0103100', 'abnormal stage I oocyte morphology', 0.4864864864864865, 5.43643956286526, 1.626270082715184, 'HP:0025461', 'Abnormal cell morphology'),
(136316, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0140267', 'abnormally necrotic multiciliated cell', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(136317, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0102768', 'abnormal ooplasm morphology', 0.4444444444444444, 3.6715585125471644, 1.2774207542365574, 'UPHENO:0086172', 'abnormal cell'),
(136318, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0101921', 'abnormal chondroblast morphology', 0.5454545454545454, 5.43643956286526, 1.7220135512398786, 'HP:0025461', 'Abnormal cell morphology'),
(136319, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0140973', 'abnormally necrotic erythroid cell', 0.4878048780487805, 5.574066539846944, 1.648956290720232, 'HP:0001871', 'Abnormality of blood and blood-forming tissues'),
(136320, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0102081', 'abnormal lymphocyte morphology', 0.46153846153846156, 5.43643956286526, 1.5840220806831131, 'HP:0025461', 'Abnormal cell morphology'),
(136321, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0103037', 'abnormal ring structure morphology', 0.4444444444444444, 3.6715585125471644, 1.2774207542365574, 'UPHENO:0086172', 'abnormal cell'),
(136322, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0140381', 'abnormally necrotic ciliated cell', 0.4864864864864865, 5.43643956286526, 1.626270082715184, 'HP:0025461', 'Abnormal cell morphology'),
(136323, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0100887', 'abnormal right-dorsal blastomere', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(136324, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0101807', 'abnormal migrating neuroblast morphology', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(136325, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0107312', 'abnormal filopodium', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(136326, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0141296', 'abnormal adherens junction morphology', 0.47058823529411764, 3.6715585125471644, 1.3144551118994765, 'UPHENO:0086172', 'abnormal cell'),
(136327, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0107398', 'abnormal apical junction complex morphology', 0.42105263157894735, 3.6715585125471644, 1.2433500608051093, 'UPHENO:0086172', 'abnormal cell'),
(136328, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0101535', 'abnormal absorptive cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(136329, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0102715', 'abnormal T cell morphology', 0.43902439024390244, 5.43643956286526, 1.5449043867452603, 'HP:0025461', 'Abnormal cell morphology'),
(136330, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0107324', 'abnormal embryonic thrombocyte', 0.40540540540540543, 5.574066539846944, 1.5032487170602729, 'UPHENO:0004459', 'abnormal hematopoietic system'),
(136331, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0101713', 'abnormal anatomical entity in vitro morphology', 0.42857142857142855, 2.7446671847279203, 1.0845671654222093, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(136332, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0100108', 'abnormal cell part', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(136333, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0139758', 'abnormally necrotic oocyte', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(136334, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0102588', 'abnormal centrosome morphology', 0.47058823529411764, 3.6715585125471644, 1.3144551118994765, 'UPHENO:0086172', 'abnormal cell'),
(136335, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0103179', 'abnormal lampbrush chromosome morphology', 0.47058823529411764, 3.6715585125471644, 1.3144551118994765, 'UPHENO:0086172', 'abnormal cell'),
(136336, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0140075', 'abnormally necrotic stem cell', 0.4864864864864865, 5.43643956286526, 1.626270082715184, 'HP:0025461', 'Abnormal cell morphology'),
(136337, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0129486', 'increased size of the cell', 0.42857142857142855, 5.43643956286526, 1.526401870347189, 'HP:0025461', 'Abnormal cell morphology'),
(136338, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0100917', 'abnormal stage III oocyte', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(136339, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0140803', 'abnormally necrotic pericyte', 0.4864864864864865, 5.43643956286526, 1.626270082715184, 'HP:0025461', 'Abnormal cell morphology'),
(136340, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0140106', 'abnormally necrotic blood', 0.41025641025641024, 5.574066539846944, 1.5122157680595638, 'HP:0001871', 'Abnormality of blood and blood-forming tissues'),
(136341, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0100337', 'abnormal zygote', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(136342, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0140169', 'abnormally necrotic stage VI oocyte', 0.4186046511627907, 5.43643956286526, 1.5085486027240909, 'HP:0025461', 'Abnormal cell morphology'),
(136343, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0100823', 'abnormal blood', 0.40625, 5.574066539846944, 1.5048137864243607, 'HP:0001871', 'Abnormality of blood and blood-forming tissues'),
(136344, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0141146', 'abnormally necrotic oxygen accumulating cell', 0.4864864864864865, 5.43643956286526, 1.626270082715184, 'HP:0025461', 'Abnormal cell morphology'),
(136345, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0101136', 'abnormal ooplasm', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(136346, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0100976', 'abnormal multiciliated cell', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(136347, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0107412', 'abnormal adult thrombocyte morphology', 0.425531914893617, 5.574066539846944, 1.540111427282295, 'HP:0001871', 'Abnormality of blood and blood-forming tissues'),
(136348, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0101283', 'abnormal left-ventral blastomere', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(136349, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0129551', 'increased size of the cell part', 0.43243243243243246, 3.6715585125471644, 1.2600400701560144, 'UPHENO:0086172', 'abnormal cell'),
(136350, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0102808', 'abnormal non-ciliated epithelial cell morphology', 0.47368421052631576, 5.43643956286526, 1.6047291305419304, 'HP:0025461', 'Abnormal cell morphology'),
(136351, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0101498', 'abnormal stage II oocyte', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(136352, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0102519', 'abnormal right-dorsal blastomere morphology', 0.46153846153846156, 5.43643956286526, 1.5840220806831131, 'HP:0025461', 'Abnormal cell morphology'),
(136353, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0101113', 'abnormal stage IV oocyte', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(136354, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0102206', 'abnormal gastrula cell morphology', 0.4864864864864865, 5.43643956286526, 1.626270082715184, 'HP:0025461', 'Abnormal cell morphology'),
(136355, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0140647', 'abnormally necrotic nucleate erythrocyte', 0.4864864864864865, 5.43643956286526, 1.626270082715184, 'HP:0025461', 'Abnormal cell morphology'),
(136356, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0101228', 'abnormal mesenchymal stem cell', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(136357, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0141195', 'abnormally necrotic somatic stem cell', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(136358, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0140010', 'abnormally necrotic zygote', 0.4864864864864865, 5.43643956286526, 1.626270082715184, 'HP:0025461', 'Abnormal cell morphology'),
(136359, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0115758', 'abnormally decreased mobility of melanoblast', 0.4375, 3.6715585125471644, 1.2674016132384338, 'UPHENO:0086172', 'abnormal cell'),
(136360, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0101939', 'abnormal blastomere morphology', 0.4864864864864865, 5.43643956286526, 1.626270082715184, 'HP:0025461', 'Abnormal cell morphology'),
(136361, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0103150', 'abnormal B cell morphology', 0.43902439024390244, 5.43643956286526, 1.5449043867452603, 'HP:0025461', 'Abnormal cell morphology'),
(136362, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0127837', 'abnormally localised erythroid cell', 0.41025641025641024, 5.574066539846944, 1.5122157680595638, 'UPHENO:0004459', 'abnormal hematopoietic system'),
(136363, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0103167', 'abnormal absorptive cell morphology', 0.5454545454545454, 5.43643956286526, 1.7220135512398786, 'HP:0025461', 'Abnormal cell morphology'),
(136364, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0100477', 'abnormal pericyte', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(136365, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0141007', 'abnormally necrotic electrically active cell', 0.4864864864864865, 5.43643956286526, 1.626270082715184, 'HP:0025461', 'Abnormal cell morphology'),
(136366, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0140358', 'abnormally necrotic non-ciliated epithelial cell', 0.4186046511627907, 5.43643956286526, 1.5085486027240909, 'HP:0025461', 'Abnormal cell morphology'),
(136367, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0131667', 'abnormal actin cytoskeleton', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(136368, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0128006', 'decreased size of the cell', 0.42857142857142855, 5.43643956286526, 1.526401870347189, 'HP:0025461', 'Abnormal cell morphology'),
(136369, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0102830', 'abnormal digestive enzyme secreting cell morphology', 0.4090909090909091, 5.43643956286526, 1.491307481034791, 'HP:0025461', 'Abnormal cell morphology'),
(136370, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0100515', 'abnormal somatic stem cell', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(136371, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0102965', 'abnormal barrier epithelial cell morphology', 0.5454545454545454, 5.43643956286526, 1.7220135512398786, 'HP:0025461', 'Abnormal cell morphology'),
(136372, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0101513', 'abnormal basal body', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(136373, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0107373', 'abnormal efferent neuron morphology', 0.4186046511627907, 5.43643956286526, 1.5085486027240909, 'HP:0025461', 'Abnormal cell morphology'),
(136374, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0131687', 'abnormal astral microtubule', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(136375, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0131675', 'abnormal spindle microtubule', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(136376, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0103080', 'abnormal myelin accumulating cell morphology', 0.5454545454545454, 5.43643956286526, 1.7220135512398786, 'HP:0025461', 'Abnormal cell morphology'),
(136377, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0139969', 'abnormally necrotic primordial germ cell', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(136378, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0101450', 'abnormal myeloid cell', 0.46875, 5.574066539846944, 1.6164293026771246, 'HP:0001871', 'Abnormality of blood and blood-forming tissues'),
(136379, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0140098', 'abnormally necrotic secondary spermatogonium', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(136380, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0101409', 'abnormal perivitelline space', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(136381, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0103041', 'abnormal perivitelline space morphology', 0.4444444444444444, 3.6715585125471644, 1.2774207542365574, 'UPHENO:0086172', 'abnormal cell'),
(136382, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0141246', 'abnormally necrotic stage V oocyte', 0.4186046511627907, 5.43643956286526, 1.5085486027240909, 'HP:0025461', 'Abnormal cell morphology'),
(136383, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0102934', 'abnormal subcortical cytoplasm morphology', 0.4444444444444444, 3.6715585125471644, 1.2774207542365574, 'UPHENO:0086172', 'abnormal cell'),
(136384, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0103129', 'abnormal ciliary axoneme morphology', 0.4444444444444444, 3.6715585125471644, 1.2774207542365574, 'UPHENO:0086172', 'abnormal cell'),
(136385, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0102549', 'abnormal stage III oocyte morphology', 0.4864864864864865, 5.43643956286526, 1.626270082715184, 'HP:0025461', 'Abnormal cell morphology'),
(136386, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0102745', 'abnormal stage IV oocyte morphology', 0.4864864864864865, 5.43643956286526, 1.626270082715184, 'HP:0025461', 'Abnormal cell morphology'),
(136387, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0102181', 'abnormal mitotic cell morphology', 0.5454545454545454, 5.43643956286526, 1.7220135512398786, 'HP:0025461', 'Abnormal cell morphology'),
(136388, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0101241', 'abnormal nucleate erythrocyte', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(136389, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0101297', 'abnormal barrier cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(136390, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0101264', 'abnormal mitotic spindle', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(136391, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0102356', 'abnormal kinetochore morphology', 0.47058823529411764, 3.6715585125471644, 1.3144551118994765, 'UPHENO:0086172', 'abnormal cell'),
(136392, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0101240', 'abnormal ciliated non-epidermal cell', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(136393, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0103207', 'abnormal vitelline membrane morphology', 0.42105263157894735, 3.6715585125471644, 1.2433500608051093, 'UPHENO:0086172', 'abnormal cell'),
(136394, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0140600', 'abnormally necrotic apoptotic cell', 0.4864864864864865, 5.43643956286526, 1.626270082715184, 'HP:0025461', 'Abnormal cell morphology'),
(136395, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0103132', 'abnormal endodermal cell morphology', 0.4186046511627907, 5.43643956286526, 1.5085486027240909, 'HP:0025461', 'Abnormal cell morphology'),
(136396, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0102526', 'abnormal nucleus morphology', 0.47058823529411764, 3.6715585125471644, 1.3144551118994765, 'UPHENO:0086172', 'abnormal cell'),
(136397, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0101497', 'abnormal ciliary axoneme', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(136398, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0140589', 'abnormally necrotic keratin accumulating cell', 0.4864864864864865, 5.43643956286526, 1.626270082715184, 'HP:0025461', 'Abnormal cell morphology'),
(136399, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0100862', 'abnormal blastomere V1', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(136400, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0139929', 'abnormally necrotic barrier epithelial cell', 0.4864864864864865, 5.43643956286526, 1.626270082715184, 'HP:0025461', 'Abnormal cell morphology'),
(136401, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0100307', 'abnormal blastomere', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(136402, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0102029', 'abnormal ventral vegetal hemisphere blastomere morphology', 0.4090909090909091, 5.43643956286526, 1.491307481034791, 'HP:0025461', 'Abnormal cell morphology'),
(136403, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0101657', 'abnormal oocyte morphology', 0.5142857142857142, 5.43643956286526, 1.6720894724144628, 'HP:0025461', 'Abnormal cell morphology'),
(136404, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0102819', 'abnormal dorsolateral commissural neuron morphology', 0.42857142857142855, 5.43643956286526, 1.526401870347189, 'HP:0025461', 'Abnormal cell morphology'),
(136405, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0140868', 'abnormally necrotic chondroblast', 0.4864864864864865, 5.43643956286526, 1.626270082715184, 'HP:0025461', 'Abnormal cell morphology'),
(136406, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0102306', 'abnormal secondary oogonium morphology', 0.5142857142857142, 5.43643956286526, 1.6720894724144628, 'HP:0025461', 'Abnormal cell morphology'),
(136407, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0100172', 'abnormal stem cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(136408, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0102852', 'abnormal centriole morphology', 0.45714285714285713, 3.6715585125471644, 1.2955411026258445, 'UPHENO:0086172', 'abnormal cell'),
(136409, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0103095', 'abnormal right-ventral blastomere morphology', 0.46153846153846156, 5.43643956286526, 1.5840220806831131, 'HP:0025461', 'Abnormal cell morphology'),
(136410, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0102586', 'abnormal neural progenitor cell morphology', 0.42857142857142855, 5.43643956286526, 1.526401870347189, 'HP:0025461', 'Abnormal cell morphology'),
(136411, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0101917', 'abnormal progenitor cell morphology', 0.5454545454545454, 5.43643956286526, 1.7220135512398786, 'HP:0025461', 'Abnormal cell morphology'),
(136412, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0101468', 'abnormal stage I oocyte', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(136413, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0102693', 'abnormal plasma membrane morphology', 0.47058823529411764, 3.6715585125471644, 1.3144551118994765, 'UPHENO:0086172', 'abnormal cell'),
(136414, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0100724', 'abnormal kinetochore', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(136415, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0140580', 'abnormally necrotic migrating myoblast', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(136416, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0140505', 'abnormally necrotic stromal cell', 0.4186046511627907, 5.43643956286526, 1.5085486027240909, 'HP:0025461', 'Abnormal cell morphology'),
(136417, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0101366', 'abnormal morula cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(136418, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0101575', 'abnormal vitelline membrane', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(136419, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0102520', 'abnormal microtubule morphology', 0.47058823529411764, 3.6715585125471644, 1.3144551118994765, 'UPHENO:0086172', 'abnormal cell'),
(136420, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0102504', 'abnormal neuroendocrine cell morphology', 0.42857142857142855, 5.43643956286526, 1.526401870347189, 'HP:0025461', 'Abnormal cell morphology'),
(136421, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0102270', 'abnormal polar body morphology', 0.4090909090909091, 5.43643956286526, 1.491307481034791, 'HP:0025461', 'Abnormal cell morphology'),
(136422, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0100004', 'abnormal cell', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(136423, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0102958', 'abnormal cementoblast morphology', 0.5454545454545454, 5.43643956286526, 1.7220135512398786, 'HP:0025461', 'Abnormal cell morphology'),
(136424, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0102258', 'abnormal primordial germ cell morphology', 0.5142857142857142, 5.43643956286526, 1.6720894724144628, 'HP:0025461', 'Abnormal cell morphology'),
(136425, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0141285', 'abnormal cortical actin cytoskeleton morphology', 0.45714285714285713, 3.6715585125471644, 1.2955411026258445, 'UPHENO:0086172', 'abnormal cell'),
(136426, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0139759', 'abnormally necrotic germ cell', 0.4864864864864865, 5.43643956286526, 1.626270082715184, 'HP:0025461', 'Abnormal cell morphology'),
(136427, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0102323', 'abnormal keratin accumulating cell morphology', 0.5454545454545454, 5.43643956286526, 1.7220135512398786, 'HP:0025461', 'Abnormal cell morphology'),
(136428, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0102153', 'abnormal animal blastomere morphology', 0.42857142857142855, 5.43643956286526, 1.526401870347189, 'HP:0025461', 'Abnormal cell morphology'),
(136429, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0101821', 'abnormal enteroendocrine cell morphology', 0.42857142857142855, 5.43643956286526, 1.526401870347189, 'HP:0025461', 'Abnormal cell morphology'),
(136430, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0128071', 'decreased size of the cell part', 0.43243243243243246, 3.6715585125471644, 1.2600400701560144, 'UPHENO:0086172', 'abnormal cell'),
(136431, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0100285', 'abnormal progenitor cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(136432, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0103093', 'abnormal sperm entry point morphology', 0.45714285714285713, 3.6715585125471644, 1.2955411026258445, 'UPHENO:0086172', 'abnormal cell'),
(136433, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0100956', 'abnormal centrosome', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(136434, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0102030', 'abnormal vegetal blastomere morphology', 0.42857142857142855, 5.43643956286526, 1.526401870347189, 'HP:0025461', 'Abnormal cell morphology'),
(136435, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0140522', 'abnormally necrotic stage II oocyte', 0.4186046511627907, 5.43643956286526, 1.5085486027240909, 'HP:0025461', 'Abnormal cell morphology'),
(136436, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0100626', 'abnormal primordial germ cell', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(136437, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0127845', 'abnormally localised myeloid cell', 0.41025641025641024, 5.574066539846944, 1.5122157680595638, 'HP:0001871', 'Abnormality of blood and blood-forming tissues'),
(136438, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0102873', 'abnormal nucleate erythrocyte morphology', 0.5454545454545454, 5.43643956286526, 1.7220135512398786, 'HP:0025461', 'Abnormal cell morphology'),
(136439, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0100372', 'abnormal hematological system', 0.43333333333333335, 5.574066539846944, 1.5541649957239663, 'HP:0001871', 'Abnormality of blood and blood-forming tissues'),
(136440, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0141503', 'abnormal lymphoblast morphology', 0.46153846153846156, 5.43643956286526, 1.5840220806831131, 'HP:0025461', 'Abnormal cell morphology'),
(136441, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0140450', 'abnormally necrotic mesenchymal stem cell', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(136442, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0102794', 'abnormal stromal cell morphology', 0.46153846153846156, 5.43643956286526, 1.5840220806831131, 'HP:0025461', 'Abnormal cell morphology'),
(136443, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0101061', 'abnormal plasma membrane', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(136444, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0101220', 'abnormal centriole', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(136445, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0141478', 'abnormally necrotic lymphoblast', 0.4186046511627907, 5.43643956286526, 1.5085486027240909, 'HP:0025461', 'Abnormal cell morphology'),
(136446, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0142057', 'abnormal desmosome', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(136447, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0140471', 'abnormally necrotic multiciliated cell precursor', 0.4864864864864865, 5.43643956286526, 1.626270082715184, 'HP:0025461', 'Abnormal cell morphology'),
(136448, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0102896', 'abnormal mitotic spindle morphology', 0.47058823529411764, 3.6715585125471644, 1.3144551118994765, 'UPHENO:0086172', 'abnormal cell'),
(136449, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0126318', 'abnormally localised cell', 0.4117647058823529, 3.6715585125471644, 1.229560169755361, 'UPHENO:0086172', 'abnormal cell'),
(136450, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0140938', 'abnormally necrotic secretory epithelial cell', 0.4186046511627907, 5.43643956286526, 1.5085486027240909, 'HP:0025461', 'Abnormal cell morphology'),
(136451, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0100551', 'abnormal oocyte cortex', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(136452, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0103145', 'abnormal basal body morphology', 0.47058823529411764, 3.6715585125471644, 1.3144551118994765, 'UPHENO:0086172', 'abnormal cell'),
(136453, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0107284', 'abnormal migrating myoblast', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(136454, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0141135', 'abnormally necrotic spermatid', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(136455, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0141289', 'abnormal spindle microtubule morphology', 0.4444444444444444, 3.6715585125471644, 1.2774207542365574, 'UPHENO:0086172', 'abnormal cell'),
(136456, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0140068', 'abnormally necrotic myoblast', 0.4864864864864865, 5.43643956286526, 1.626270082715184, 'HP:0025461', 'Abnormal cell morphology'),
(136457, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0100691', 'abnormal keratin accumulating cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(136458, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0102621', 'abnormal right blastomere morphology', 0.46153846153846156, 5.43643956286526, 1.5840220806831131, 'HP:0025461', 'Abnormal cell morphology'),
(136459, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0107323', 'abnormal thrombocyte', 0.4166666666666667, 5.574066539846944, 1.523984161642183, 'HP:0001871', 'Abnormality of blood and blood-forming tissues'),
(136460, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0102704', 'abnormal mitochondrial cloud morphology', 0.4444444444444444, 3.6715585125471644, 1.2774207542365574, 'UPHENO:0086172', 'abnormal cell'),
(136461, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0102474', 'abnormal left-dorsal blastomere morphology', 0.46153846153846156, 5.43643956286526, 1.5840220806831131, 'HP:0025461', 'Abnormal cell morphology'),
(136462, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0102183', 'abnormal oocyte cortex morphology', 0.4444444444444444, 3.6715585125471644, 1.2774207542365574, 'UPHENO:0086172', 'abnormal cell'),
(136463, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0103067', 'abnormal paracrine cell morphology', 0.5454545454545454, 5.43643956286526, 1.7220135512398786, 'HP:0025461', 'Abnormal cell morphology'),
(136464, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0100549', 'abnormal mitotic cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(136465, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0102061', 'abnormal spermatid morphology', 0.5142857142857142, 5.43643956286526, 1.6720894724144628, 'HP:0025461', 'Abnormal cell morphology'),
(136466, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0102353', 'abnormal centromere morphology', 0.47058823529411764, 3.6715585125471644, 1.3144551118994765, 'UPHENO:0086172', 'abnormal cell'),
(136467, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0102285', 'abnormal myoblast morphology', 0.5454545454545454, 5.43643956286526, 1.7220135512398786, 'HP:0025461', 'Abnormal cell morphology'),
(136468, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0103010', 'abnormal blastomere D1 morphology', 0.46153846153846156, 5.43643956286526, 1.5840220806831131, 'HP:0025461', 'Abnormal cell morphology'),
(136469, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0100894', 'abnormal nucleus', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(136470, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0128249', 'decreased size of the erythroid cell', 0.40816326530612246, 5.574066539846944, 1.5083531416540121, 'UPHENO:0004459', 'abnormal hematopoietic system'),
(136471, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0102915', 'abnormal left-ventral blastomere morphology', 0.46153846153846156, 5.43643956286526, 1.5840220806831131, 'HP:0025461', 'Abnormal cell morphology'),
(136472, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0102534', 'abnormal spermatocyte morphology', 0.5142857142857142, 5.43643956286526, 1.6720894724144628, 'HP:0025461', 'Abnormal cell morphology'),
(136473, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0101897', 'abnormal sensory epithelial cell morphology', 0.47368421052631576, 5.43643956286526, 1.6047291305419304, 'HP:0025461', 'Abnormal cell morphology'),
(136474, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0100025', 'abnormal oocyte', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(136475, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0101472', 'abnormal zygote cortex', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(136476, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0102455', 'abnormal blood morphology', 0.4444444444444444, 5.574066539846944, 1.573964074113079, 'UPHENO:0004459', 'abnormal hematopoietic system'),
(136477, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0107410', 'abnormal thrombocyte morphology', 0.4444444444444444, 5.574066539846944, 1.573964074113079, 'HP:0001871', 'Abnormality of blood and blood-forming tissues'),
(136478, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0141288', 'abnormal astral microtubule morphology', 0.42105263157894735, 3.6715585125471644, 1.2433500608051093, 'UPHENO:0086172', 'abnormal cell'),
(136479, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0102869', 'abnormal mucus secreting cell morphology', 0.5454545454545454, 5.43643956286526, 1.7220135512398786, 'HP:0025461', 'Abnormal cell morphology'),
(136480, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0139780', 'abnormally necrotic neuron', 0.4090909090909091, 5.43643956286526, 1.491307481034791, 'HP:0025461', 'Abnormal cell morphology'),
(136481, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0129729', 'increased size of the erythroid cell', 0.40816326530612246, 5.574066539846944, 1.5083531416540121, 'HP:0001871', 'Abnormality of blood and blood-forming tissues'),
(136482, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0140533', 'abnormally necrotic myelin accumulating cell', 0.4864864864864865, 5.43643956286526, 1.626270082715184, 'HP:0025461', 'Abnormal cell morphology'),
(136483, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0101467', 'abnormal alkali secreting cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(136484, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0102625', 'abnormal ligament cell morphology', 0.42857142857142855, 5.43643956286526, 1.526401870347189, 'HP:0025461', 'Abnormal cell morphology'),
(136485, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0133438', 'abnormal cilium morphology in the ciliated non-epidermal cell', 0.43243243243243246, 3.6715585125471644, 1.2600400701560144, 'UPHENO:0086172', 'abnormal cell'),
(136486, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0139888', 'abnormally necrotic glial cell', 0.4090909090909091, 5.43643956286526, 1.491307481034791, 'HP:0025461', 'Abnormal cell morphology'),
(136487, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0100721', 'abnormal centromere', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(136488, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0102386', 'abnormal electrically active cell morphology', 0.5454545454545454, 5.43643956286526, 1.7220135512398786, 'HP:0025461', 'Abnormal cell morphology'),
(136489, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0101480', 'abnormal stage V oocyte', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(136490, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0102539', 'abnormal cytoplasm morphology', 0.47058823529411764, 3.6715585125471644, 1.3144551118994765, 'UPHENO:0086172', 'abnormal cell'),
(136491, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0102434', 'abnormal exocrine cell morphology', 0.5454545454545454, 5.43643956286526, 1.7220135512398786, 'HP:0025461', 'Abnormal cell morphology'),
(136492, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0102004', 'abnormal hematological system morphology', 0.4444444444444444, 5.574066539846944, 1.573964074113079, 'HP:0001871', 'Abnormality of blood and blood-forming tissues'),
(136493, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0102994', 'abnormal vegetal cortex morphology', 0.43243243243243246, 3.6715585125471644, 1.2600400701560144, 'UPHENO:0086172', 'abnormal cell'),
(136494, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0102929', 'abnormal barrier cell morphology', 0.5454545454545454, 5.43643956286526, 1.7220135512398786, 'HP:0025461', 'Abnormal cell morphology'),
(136495, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0103219', 'abnormal hemangioblast morphology', 0.5405405405405406, 5.574066539846944, 1.735802102907416, 'UPHENO:0004459', 'abnormal hematopoietic system'),
(136496, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0102496', 'abnormal dorsolateral ascending neuron morphology', 0.42857142857142855, 5.43643956286526, 1.526401870347189, 'HP:0025461', 'Abnormal cell morphology'),
(136497, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0140328', 'abnormally necrotic secondary oogonium', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(136498, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0101107', 'abnormal erythroid cell', 0.46875, 5.574066539846944, 1.6164293026771246, 'HP:0001871', 'Abnormality of blood and blood-forming tissues'),
(136499, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0103021', 'abnormal wedge region morphology', 0.4444444444444444, 3.6715585125471644, 1.2774207542365574, 'UPHENO:0086172', 'abnormal cell'),
(136500, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0101461', 'abnormal sperm entry point', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(136501, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0102416', 'abnormal left blastomere morphology', 0.46153846153846156, 5.43643956286526, 1.5840220806831131, 'HP:0025461', 'Abnormal cell morphology'),
(136502, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0141277', 'abnormal actin cytoskeleton morphology', 0.47058823529411764, 3.6715585125471644, 1.3144551118994765, 'UPHENO:0086172', 'abnormal cell'),
(136503, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0129839', 'increased size of the myeloid cell', 0.40816326530612246, 5.574066539846944, 1.5083531416540121, 'UPHENO:0004459', 'abnormal hematopoietic system'),
(136504, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0102494', 'abnormal blastomere V1 morphology', 0.46153846153846156, 5.43643956286526, 1.5840220806831131, 'HP:0025461', 'Abnormal cell morphology'),
(136505, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0102347', 'abnormal ciliated cell morphology', 0.5454545454545454, 5.43643956286526, 1.7220135512398786, 'HP:0025461', 'Abnormal cell morphology'),
(136506, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0101667', 'abnormal ventral animal hemisphere blastomere morphology', 0.4090909090909091, 5.43643956286526, 1.491307481034791, 'HP:0025461', 'Abnormal cell morphology'),
(136507, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0142064', 'abnormal desmosome morphology', 0.47058823529411764, 3.6715585125471644, 1.3144551118994765, 'UPHENO:0086172', 'abnormal cell'),
(136508, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0101968', 'abnormal interneuron morphology', 0.4186046511627907, 5.43643956286526, 1.5085486027240909, 'HP:0025461', 'Abnormal cell morphology'),
(136509, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0100704', 'abnormal Merkel cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(136510, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0102531', 'abnormal secondary spermatogonium morphology', 0.5142857142857142, 5.43643956286526, 1.6720894724144628, 'HP:0025461', 'Abnormal cell morphology'),
(136511, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0102028', 'abnormal dorsal animal hemisphere blastomere morphology', 0.4090909090909091, 5.43643956286526, 1.491307481034791, 'HP:0025461', 'Abnormal cell morphology'),
(136512, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0100218', 'abnormal epithelial cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(136513, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0103005', 'abnormal oxygen accumulating cell morphology', 0.5454545454545454, 5.43643956286526, 1.7220135512398786, 'HP:0025461', 'Abnormal cell morphology'),
(136514, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0101835', 'abnormal endocrine cell morphology', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(136515, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0102800', 'abnormal circulating cell morphology', 0.43902439024390244, 5.43643956286526, 1.5449043867452603, 'HP:0025461', 'Abnormal cell morphology'),
(136516, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0102147', 'abnormal somatic stem cell morphology', 0.5142857142857142, 5.43643956286526, 1.6720894724144628, 'HP:0025461', 'Abnormal cell morphology'),
(136517, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0100503', 'abnormal blastomere D2', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(136518, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0102047', 'abnormal secretory epithelial cell morphology', 0.47368421052631576, 5.43643956286526, 1.6047291305419304, 'HP:0025461', 'Abnormal cell morphology'),
(136519, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0100638', 'abnormal polar body', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(136520, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0102871', 'abnormal olfactory epithelial support cell morphology', 0.4186046511627907, 5.43643956286526, 1.5085486027240909, 'HP:0025461', 'Abnormal cell morphology'),
(136521, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0101658', 'abnormal germ cell morphology', 0.5454545454545454, 5.43643956286526, 1.7220135512398786, 'HP:0025461', 'Abnormal cell morphology'),
(136522, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0101389', 'abnormal wedge region', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(136523, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0107399', 'abnormal filopodium morphology', 0.47058823529411764, 3.6715585125471644, 1.3144551118994765, 'UPHENO:0086172', 'abnormal cell'),
(136524, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0140239', 'abnormally necrotic absorptive cell', 0.4864864864864865, 5.43643956286526, 1.626270082715184, 'HP:0025461', 'Abnormal cell morphology'),
(136525, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0102069', 'abnormal proepicardium morphology', 0.5142857142857142, 5.43643956286526, 1.6720894724144628, 'HP:0025461', 'Abnormal cell morphology'),
(136526, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0139839', 'abnormally necrotic progenitor cell', 0.4864864864864865, 5.43643956286526, 1.626270082715184, 'HP:0025461', 'Abnormal cell morphology'),
(136527, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0100533', 'abnormal melanoblast', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(136528, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0140278', 'abnormally necrotic Merkel cell', 0.4864864864864865, 5.43643956286526, 1.626270082715184, 'HP:0025461', 'Abnormal cell morphology'),
(136529, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0107374', 'abnormal afferent neuron morphology', 0.4186046511627907, 5.43643956286526, 1.5085486027240909, 'HP:0025461', 'Abnormal cell morphology'),
(136530, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0140747', 'abnormally necrotic morula cell', 0.42857142857142855, 5.43643956286526, 1.526401870347189, 'HP:0025461', 'Abnormal cell morphology'),
(136531, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0102608', 'abnormal multiciliated cell morphology', 0.5142857142857142, 5.43643956286526, 1.6720894724144628, 'HP:0025461', 'Abnormal cell morphology'),
(136532, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0101804', 'abnormal stem cell morphology', 0.5454545454545454, 5.43643956286526, 1.7220135512398786, 'HP:0025461', 'Abnormal cell morphology'),
(136533, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0141147', 'abnormally necrotic alkali secreting cell', 0.4864864864864865, 5.43643956286526, 1.626270082715184, 'HP:0025461', 'Abnormal cell morphology'),
(136534, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0101435', 'abnormal paracrine cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(136535, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0101004', 'abnormal acid secreting cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(136536, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0107325', 'abnormal adult thrombocyte', 0.40540540540540543, 5.574066539846944, 1.5032487170602729, 'UPHENO:0004459', 'abnormal hematopoietic system'),
(136537, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0102765', 'abnormal motor neuron morphology', 0.42857142857142855, 5.43643956286526, 1.526401870347189, 'HP:0025461', 'Abnormal cell morphology'),
(136538, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0100026', 'abnormal germ cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(136539, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0101587', 'abnormal hemangioblast', 0.46875, 5.574066539846944, 1.6164293026771246, 'HP:0001871', 'Abnormality of blood and blood-forming tissues'),
(136540, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0139717', 'abnormally necrotic cell', 0.5294117647058824, 5.43643956286526, 1.696500828969256, 'HP:0025461', 'Abnormal cell morphology'),
(136541, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0141154', 'abnormally necrotic barrier cell', 0.4864864864864865, 5.43643956286526, 1.626270082715184, 'HP:0025461', 'Abnormal cell morphology'),
(136542, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0139734', 'abnormally necrotic blastomere', 0.42857142857142855, 5.43643956286526, 1.526401870347189, 'HP:0025461', 'Abnormal cell morphology'),
(136543, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0102113', 'abnormal anatomical line morphology', 0.42857142857142855, 2.7446671847279203, 1.0845671654222093, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(136544, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0100289', 'abnormal chondroblast', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(136545, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0102514', 'abnormal perichondrial cell morphology', 0.4090909090909091, 5.43643956286526, 1.491307481034791, 'HP:0025461', 'Abnormal cell morphology'),
(136546, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0101976', 'abnormal portion of organism substance morphology', 0.42857142857142855, 2.7446671847279203, 1.0845671654222093, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(136547, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0107411', 'abnormal embryonic thrombocyte morphology', 0.425531914893617, 5.574066539846944, 1.540111427282295, 'HP:0001871', 'Abnormality of blood and blood-forming tissues'),
(136548, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0100547', 'abnormal blastomere V2', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(136549, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0101850', 'abnormal epithelial cell morphology', 0.5, 5.43643956286526, 1.6487024538808177, 'HP:0025461', 'Abnormal cell morphology'),
(136550, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0139981', 'abnormally necrotic early embryonic cell', 0.46153846153846156, 5.43643956286526, 1.5840220806831131, 'HP:0025461', 'Abnormal cell morphology'),
(136551, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0100674', 'abnormal secondary oogonium', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(136552, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0101072', 'abnormal mitochondrial cloud', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(136553, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0127774', 'abnormally localised hemangioblast', 0.41025641025641024, 5.574066539846944, 1.5122157680595638, 'HP:0001871', 'Abnormality of blood and blood-forming tissues'),
(136554, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0103082', 'abnormal myeloid cell morphology', 0.5405405405405406, 5.574066539846944, 1.735802102907416, 'UPHENO:0004459', 'abnormal hematopoietic system'),
(136555, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0140331', 'abnormally necrotic myeloid cell', 0.4878048780487805, 5.574066539846944, 1.648956290720232, 'HP:0001871', 'Abnormality of blood and blood-forming tissues'),
(136556, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0103112', 'abnormal stage V oocyte morphology', 0.4864864864864865, 5.43643956286526, 1.626270082715184, 'HP:0025461', 'Abnormal cell morphology'),
(136557, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0140096', 'abnormally necrotic gastrula cell', 0.42857142857142855, 5.43643956286526, 1.526401870347189, 'HP:0025461', 'Abnormal cell morphology'),
(136558, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0101940', 'abnormal early embryonic cell morphology', 0.5142857142857142, 5.43643956286526, 1.6720894724144628, 'HP:0025461', 'Abnormal cell morphology'),
(136559, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0101326', 'abnormal cementoblast', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(136560, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0100784', 'abnormal left blastomere', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(136561, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0102872', 'abnormal ciliated non-epidermal cell morphology', 0.5142857142857142, 5.43643956286526, 1.6720894724144628, 'HP:0025461', 'Abnormal cell morphology'),
(136562, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0141048', 'abnormally necrotic mitotic cell', 0.4864864864864865, 5.43643956286526, 1.626270082715184, 'HP:0025461', 'Abnormal cell morphology'),
(136563, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0141203', 'abnormally necrotic exocrine cell', 0.4864864864864865, 5.43643956286526, 1.626270082715184, 'HP:0025461', 'Abnormal cell morphology'),
(136564, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0100754', 'abnormal electrically active cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(136565, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0141166', 'abnormally necrotic stage III oocyte', 0.4186046511627907, 5.43643956286526, 1.5085486027240909, 'HP:0025461', 'Abnormal cell morphology'),
(136566, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0141314', 'abnormal Roux spot morphology', 0.4444444444444444, 3.6715585125471644, 1.2774207542365574, 'UPHENO:0086172', 'abnormal cell'),
(136567, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0100899', 'abnormal secondary spermatogonium', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(136568, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0140622', 'abnormally necrotic migrating neuroblast', 0.4090909090909091, 5.43643956286526, 1.491307481034791, 'HP:0025461', 'Abnormal cell morphology'),
(136569, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0102165', 'abnormal melanoblast morphology', 0.5454545454545454, 5.43643956286526, 1.7220135512398786, 'HP:0025461', 'Abnormal cell morphology'),
(136570, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0131669', 'abnormal Roux spot', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(136571, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0128359', 'decreased size of the myeloid cell', 0.40816326530612246, 5.574066539846944, 1.5083531416540121, 'UPHENO:0004459', 'abnormal hematopoietic system'),
(136572, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0100888', 'abnormal microtubule', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(136573, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0107339', 'abnormal yolk platelet', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(136574, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0100653', 'abnormal myoblast', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(136575, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0102109', 'abnormal pericyte morphology', 0.5454545454545454, 5.43643956286526, 1.7220135512398786, 'HP:0025461', 'Abnormal cell morphology'),
(136576, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0101808', 'abnormal stage VI oocyte morphology', 0.4864864864864865, 5.43643956286526, 1.626270082715184, 'HP:0025461', 'Abnormal cell morphology'),
(136577, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0100437', 'abnormal proepicardium', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(136578, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0102179', 'abnormal blastomere V2 morphology', 0.46153846153846156, 5.43643956286526, 1.5840220806831131, 'HP:0025461', 'Abnormal cell morphology'),
(136579, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0102334', 'abnormal glial cell morphology', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(136580, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0131677', 'abnormal actin filament', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(136581, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0140451', 'abnormally necrotic sensory epithelial cell', 0.4186046511627907, 5.43643956286526, 1.5085486027240909, 'HP:0025461', 'Abnormal cell morphology'),
(136582, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0101071', 'abnormal endoplasmic reticulum', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(136583, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0142067', 'abnormally necrotic desmosome', 0.43243243243243246, 3.6715585125471644, 1.2600400701560144, 'UPHENO:0086172', 'abnormal cell'),
(136584, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0100429', 'abnormal spermatid', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(136585, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0139838', 'abnormally necrotic proepicardium', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(136586, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0101333', 'abnormal barrier epithelial cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(136587, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0101463', 'abnormal right-ventral blastomere', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(136588, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0100392', 'abnormal cilium', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(136589, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0101740', 'abnormal cell part morphology', 0.5, 3.6715585125471644, 1.3549093166236559, 'UPHENO:0086172', 'abnormal cell'),
(136590, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0131685', 'abnormal cortical actin cytoskeleton', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(136591, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0140429', 'abnormally necrotic hemangioblast', 0.4878048780487805, 5.574066539846944, 1.648956290720232, 'HP:0001871', 'Abnormality of blood and blood-forming tissues'),
(136592, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0102141', 'abnormal germ plasm morphology', 0.41025641025641024, 3.6715585125471644, 1.2273061620492112, 'UPHENO:0086172', 'abnormal cell'),
(136593, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0100842', 'abnormal left-dorsal blastomere', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(136594, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0140459', 'abnormally necrotic thrombocyte', 0.40816326530612246, 5.574066539846944, 1.5083531416540121, 'UPHENO:0004459', 'abnormal hematopoietic system'),
(136595, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0102333', 'abnormal microglial cell morphology', 0.42857142857142855, 5.43643956286526, 1.526401870347189, 'HP:0025461', 'Abnormal cell morphology'),
(136596, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0107426', 'abnormal yolk platelet morphology', 0.4444444444444444, 3.6715585125471644, 1.2774207542365574, 'UPHENO:0086172', 'abnormal cell'),
(136597, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0141023', 'abnormally necrotic ciliated non-epidermal cell', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(136598, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0101948', 'abnormal gamete morphology', 0.4090909090909091, 5.43643956286526, 1.491307481034791, 'HP:0025461', 'Abnormal cell morphology'),
(136599, 'HP:0012130', 'Abnormal erythroid lineage cell morphology', 'XPO:0140752', 'abnormally necrotic melanoblast', 0.4864864864864865, 5.43643956286526, 1.626270082715184, 'HP:0025461', 'Abnormal cell morphology'),
(136600, 'HP:0009979', 'Complete duplication of the middle phalanx of the 4th finger', 'XPO:0103609', 'abnormally increased number of forelimb digit in the regenerating forelimb', 0.556390977443609, 12.167655724266345, 2.6019173433492995, 'HP:0001161', 'Hand polydactyly'),
(136601, 'HP:0009979', 'Complete duplication of the middle phalanx of the 4th finger', 'XPO:0115788', 'duplicated forelimb digit 4 in regenerating forelimb', 0.5362318840579711, 12.167655724266345, 2.554346286937638, 'HP:0001161', 'Hand polydactyly'),
(136602, 'HP:0009979', 'Complete duplication of the middle phalanx of the 4th finger', 'XPO:0103634', 'abnormally increased number of forelimb digit', 0.5826771653543307, 12.167655724266345, 2.6626706793035653, 'HP:0001161', 'Hand polydactyly'),
(136603, 'HP:0009979', 'Complete duplication of the middle phalanx of the 4th finger', 'XPO:0115786', 'duplicated forelimb digit 2 in regenerating forelimb', 0.5362318840579711, 12.167655724266345, 2.554346286937638, 'HP:0001161', 'Hand polydactyly'),
(136604, 'HP:0009979', 'Complete duplication of the middle phalanx of the 4th finger', 'XPO:0115787', 'duplicated forelimb digit 3 in regenerating forelimb', 0.5362318840579711, 12.167655724266345, 2.554346286937638, 'HP:0001161', 'Hand polydactyly'),
(136605, 'HP:0009979', 'Complete duplication of the middle phalanx of the 4th finger', 'XPO:0115789', 'duplicated forelimb digit 5 in regenerating forelimb', 0.5362318840579711, 12.167655724266345, 2.554346286937638, 'HP:0001161', 'Hand polydactyly'),
(136606, 'HP:0034477', 'Perihepatic adhesions', 'XPO:0100572', 'abnormal branchial arch', 0.40540540540540543, 5.05060299610679, 1.4309233924911664, 'HP:0025031', 'Abnormality of the digestive system'),
(136607, 'HP:0034477', 'Perihepatic adhesions', 'XPO:0100621', 'abnormal peritoneum', 0.53125, 10.854497839006713, 2.401343785669248, 'HP:0004298', 'Abnormality of the abdominal wall'),
(136608, 'HP:0034477', 'Perihepatic adhesions', 'XPO:0100591', 'abnormal pharyngeal arch', 0.4166666666666667, 5.05060299610679, 1.45066119926208, 'HP:0025031', 'Abnormality of the digestive system'),
(136609, 'HP:0034477', 'Perihepatic adhesions', 'XPO:0100156', 'abnormal foregut', 0.4838709677419355, 5.05060299610679, 1.5632786569919361, 'HP:0025031', 'Abnormality of the digestive system'),
(136610, 'HP:0034477', 'Perihepatic adhesions', 'XPO:0100523', 'abnormal midgut', 0.4838709677419355, 5.05060299610679, 1.5632786569919361, 'HP:0025031', 'Abnormality of the digestive system'),
(136611, 'HP:0034477', 'Perihepatic adhesions', 'XPO:0101103', 'abnormal pharyngeal mesenchyme', 0.40540540540540543, 5.05060299610679, 1.4309233924911664, 'HP:0025031', 'Abnormality of the digestive system'),
(136612, 'HP:0034477', 'Perihepatic adhesions', 'XPO:0107305', 'abnormal dorsal posterior hindgut endoderm', 0.4166666666666667, 5.05060299610679, 1.45066119926208, 'HP:0025031', 'Abnormality of the digestive system'),
(136613, 'HP:0034477', 'Perihepatic adhesions', 'XPO:0102253', 'abnormal peritoneum morphology', 0.5, 12.568193653850074, 2.5068100899200636, 'HP:0002585', 'Abnormal peritoneum morphology'),
(136614, 'HP:0034477', 'Perihepatic adhesions', 'XPO:0100486', 'abnormal oral evagination', 0.4838709677419355, 5.05060299610679, 1.5632786569919361, 'HP:0025031', 'Abnormality of the digestive system'),
(136615, 'HP:0034477', 'Perihepatic adhesions', 'XPO:0115392', 'abnormally incomplete structure of alimentary system', 0.42105263157894735, 5.05060299610679, 1.4582762710032966, 'HP:0025031', 'Abnormality of the digestive system'),
(136616, 'HP:0034477', 'Perihepatic adhesions', 'XPO:0107288', 'abnormal larval alimentary system', 0.5172413793103449, 5.05060299610679, 1.6162861318637973, 'HP:0025031', 'Abnormality of the digestive system'),
(136617, 'HP:0034477', 'Perihepatic adhesions', 'XPO:0101084', 'abnormal mesentery', 0.4857142857142857, 10.854497839006713, 2.296123834783395, 'HP:0004298', 'Abnormality of the abdominal wall'),
(136618, 'HP:0034477', 'Perihepatic adhesions', 'XPO:0100718', 'abnormal ventral pancreatic bud', 0.45454545454545453, 5.05060299610679, 1.5151662069205463, 'HP:0025031', 'Abnormality of the digestive system'),
(136619, 'HP:0034477', 'Perihepatic adhesions', 'XPO:0102716', 'abnormal mesentery morphology', 0.42, 12.568193653850074, 2.297529397987549, 'HP:0002585', 'Abnormal peritoneum morphology'),
(136620, 'HP:0034477', 'Perihepatic adhesions', 'XPO:0101101', 'abnormal posterior foregut', 0.46875, 5.05060299610679, 1.5386585568036393, 'HP:0025031', 'Abnormality of the digestive system'),
(136621, 'HP:0034477', 'Perihepatic adhesions', 'XPO:0102125', 'abnormal liver and biliary system morphology', 0.41025641025641024, 5.05060299610679, 1.4394590146346793, 'HP:0025031', 'Abnormality of the digestive system'),
(136622, 'HP:0034477', 'Perihepatic adhesions', 'XPO:0131683', 'abnormal stomach epithelium', 0.4166666666666667, 5.05060299610679, 1.45066119926208, 'HP:0025031', 'Abnormality of the digestive system'),
(136623, 'HP:0034477', 'Perihepatic adhesions', 'XPO:0107307', 'abnormal posterior hindgut endoderm', 0.42857142857142855, 5.05060299610679, 1.471238981671103, 'HP:0025031', 'Abnormality of the digestive system'),
(136624, 'HP:0034477', 'Perihepatic adhesions', 'XPO:0131673', 'abnormal buccopharyngeal membrane', 0.40540540540540543, 5.05060299610679, 1.4309233924911664, 'HP:0025031', 'Abnormality of the digestive system'),
(136625, 'HP:0034477', 'Perihepatic adhesions', 'XPO:0101021', 'abnormal dorsal foregut', 0.46875, 5.05060299610679, 1.5386585568036393, 'HP:0025031', 'Abnormality of the digestive system'),
(136626, 'HP:0034477', 'Perihepatic adhesions', 'XPO:0100215', 'abnormal first pancreatic bud', 0.4411764705882353, 5.05060299610679, 1.4927180591674907, 'HP:0025031', 'Abnormality of the digestive system'),
(136627, 'HP:0034477', 'Perihepatic adhesions', 'XPO:0101601', 'abnormal proctodeum', 0.45454545454545453, 5.05060299610679, 1.5151662069205463, 'HP:0025031', 'Abnormality of the digestive system'),
(136628, 'HP:0034477', 'Perihepatic adhesions', 'XPO:0100454', 'abnormal lung bud', 0.40540540540540543, 5.05060299610679, 1.4309233924911664, 'HP:0025031', 'Abnormality of the digestive system'),
(136629, 'HP:0034477', 'Perihepatic adhesions', 'XPO:0101381', 'abnormal ventral foregut', 0.46875, 5.05060299610679, 1.5386585568036393, 'HP:0025031', 'Abnormality of the digestive system'),
(136630, 'HP:0034477', 'Perihepatic adhesions', 'XPO:0100494', 'abnormal liver diverticulum', 0.40540540540540543, 5.05060299610679, 1.4309233924911664, 'HP:0025031', 'Abnormality of the digestive system'),
(136631, 'HP:0034477', 'Perihepatic adhesions', 'XPO:0100492', 'abnormal gall bladder primordium', 0.4411764705882353, 5.05060299610679, 1.4927180591674907, 'HP:0025031', 'Abnormality of the digestive system'),
(136632, 'HP:0034477', 'Perihepatic adhesions', 'XPO:0100735', 'abnormal hindgut', 0.4838709677419355, 5.05060299610679, 1.5632786569919361, 'HP:0025031', 'Abnormality of the digestive system'),
(136633, 'HP:0034477', 'Perihepatic adhesions', 'XPO:0100152', 'abnormal alimentary system', 0.5357142857142857, 5.05060299610679, 1.6448951870820767, 'HP:0025031', 'Abnormality of the digestive system'),
(136634, 'HP:0034477', 'Perihepatic adhesions', 'XPO:0101198', 'abnormal digestive enzyme secreting cell', 0.4411764705882353, 5.05060299610679, 1.4927180591674907, 'HP:0025031', 'Abnormality of the digestive system'),
(136635, 'HP:0034477', 'Perihepatic adhesions', 'XPO:0100188', 'abnormal delta cell', 0.40540540540540543, 5.05060299610679, 1.4309233924911664, 'HP:0025031', 'Abnormality of the digestive system'),
(136636, 'HP:0034477', 'Perihepatic adhesions', 'XPO:0107304', 'abnormal hindgut endoderm', 0.4411764705882353, 5.05060299610679, 1.4927180591674907, 'HP:0025031', 'Abnormality of the digestive system'),
(136637, 'HP:0034477', 'Perihepatic adhesions', 'XPO:0107306', 'abnormal ventral posterior hindgut endoderm', 0.4166666666666667, 5.05060299610679, 1.45066119926208, 'HP:0025031', 'Abnormality of the digestive system'),
(136638, 'HP:0034477', 'Perihepatic adhesions', 'XPO:0100893', 'abnormal hyoid arch', 0.40540540540540543, 5.05060299610679, 1.4309233924911664, 'HP:0025031', 'Abnormality of the digestive system'),
(136639, 'HP:0034477', 'Perihepatic adhesions', 'XPO:0126967', 'abnormally localised peritoneum', 0.40476190476190477, 10.854497839006713, 2.096064698560218, 'HP:0004298', 'Abnormality of the abdominal wall'),
(136640, 'HP:0034477', 'Perihepatic adhesions', 'XPO:0100986', 'abnormal gut epithelium', 0.46875, 5.05060299610679, 1.5386585568036393, 'HP:0025031', 'Abnormality of the digestive system'),
(136641, 'HP:0034477', 'Perihepatic adhesions', 'XPO:0101377', 'abnormal manicotto glandulare', 0.4838709677419355, 5.05060299610679, 1.5632786569919361, 'HP:0025031', 'Abnormality of the digestive system'),
(136642, 'HP:0034477', 'Perihepatic adhesions', 'XPO:0100890', 'abnormal pharyngeal cavity', 0.5, 5.05060299610679, 1.5891197242666757, 'HP:0025031', 'Abnormality of the digestive system'),
(136643, 'HP:0034477', 'Perihepatic adhesions', 'XPO:0101169', 'abnormal hepato-pancreatic duct', 0.45454545454545453, 5.05060299610679, 1.5151662069205463, 'HP:0025031', 'Abnormality of the digestive system'),
(136644, 'HP:0034477', 'Perihepatic adhesions', 'XPO:0128541', 'decreased size of the peritoneum', 0.42, 12.568193653850074, 2.297529397987549, 'HP:0002585', 'Abnormal peritoneum morphology'),
(136645, 'HP:0034477', 'Perihepatic adhesions', 'XPO:0142054', 'abnormal digestive tract', 0.5, 5.05060299610679, 1.5891197242666757, 'HP:0025031', 'Abnormality of the digestive system'),
(136646, 'HP:0034477', 'Perihepatic adhesions', 'XPO:0107375', 'abnormal larval alimentary system morphology', 0.41025641025641024, 5.05060299610679, 1.4394590146346793, 'HP:0025031', 'Abnormality of the digestive system'),
(136647, 'HP:0034477', 'Perihepatic adhesions', 'XPO:0126466', 'abnormally localised alimentary system', 0.40540540540540543, 5.05060299610679, 1.4309233924911664, 'HP:0025031', 'Abnormality of the digestive system'),
(136648, 'HP:0034477', 'Perihepatic adhesions', 'XPO:0115495', 'abnormally protruding proctodeum', 0.4166666666666667, 5.05060299610679, 1.45066119926208, 'HP:0025031', 'Abnormality of the digestive system'),
(136649, 'HP:0034477', 'Perihepatic adhesions', 'XPO:0102522', 'abnormal pharyngeal cavity morphology', 0.43243243243243246, 5.05060299610679, 1.4778513250178418, 'HP:0025031', 'Abnormality of the digestive system'),
(136650, 'HP:0034477', 'Perihepatic adhesions', 'XPO:0130021', 'increased size of the peritoneum', 0.42, 12.568193653850074, 2.297529397987549, 'HP:0002585', 'Abnormal peritoneum morphology'),
(136651, 'HP:0034477', 'Perihepatic adhesions', 'XPO:0140063', 'abnormally necrotic peritoneum', 0.4375, 12.568193653850074, 2.3449061225472136, 'HP:0002585', 'Abnormal peritoneum morphology'),
(136652, 'HP:0034477', 'Perihepatic adhesions', 'XPO:0141717', 'abnormal tracheoesophageal fold', 0.42857142857142855, 5.05060299610679, 1.471238981671103, 'HP:0025031', 'Abnormality of the digestive system'),
(136653, 'HP:0034477', 'Perihepatic adhesions', 'XPO:0131662', 'abnormal foregut epithelium', 0.4166666666666667, 5.05060299610679, 1.45066119926208, 'HP:0025031', 'Abnormality of the digestive system'),
(136654, 'HP:0034477', 'Perihepatic adhesions', 'XPO:0100462', 'abnormal anterior foregut', 0.46875, 5.05060299610679, 1.5386585568036393, 'HP:0025031', 'Abnormality of the digestive system'),
(136655, 'HP:0034477', 'Perihepatic adhesions', 'XPO:0100216', 'abnormal hepato-pancreatic progenitor cell', 0.4166666666666667, 5.05060299610679, 1.45066119926208, 'HP:0025031', 'Abnormality of the digestive system'),
(136656, 'HP:0034477', 'Perihepatic adhesions', 'XPO:0115391', 'abnormally undifferentiated alimentary system', 0.5172413793103449, 5.05060299610679, 1.6162861318637973, 'HP:0025031', 'Abnormality of the digestive system'),
(136657, 'HP:0034477', 'Perihepatic adhesions', 'XPO:0127393', 'abnormally localised pharyngeal cavity', 0.40540540540540543, 5.05060299610679, 1.4309233924911664, 'HP:0025031', 'Abnormality of the digestive system'),
(136658, 'HP:0034477', 'Perihepatic adhesions', 'XPO:0142061', 'abnormal digestive tract morphology', 0.41025641025641024, 5.05060299610679, 1.4394590146346793, 'HP:0025031', 'Abnormality of the digestive system'),
(136659, 'HP:0034477', 'Perihepatic adhesions', 'XPO:0100130', 'abnormal mouth primordium', 0.4166666666666667, 5.05060299610679, 1.45066119926208, 'HP:0025031', 'Abnormality of the digestive system'),
(136660, 'HP:0034477', 'Perihepatic adhesions', 'XPO:0141833', 'edematous alimentary system', 0.41025641025641024, 5.05060299610679, 1.4394590146346793, 'HP:0025031', 'Abnormality of the digestive system'),
(136661, 'HP:0034477', 'Perihepatic adhesions', 'XPO:0100493', 'abnormal liver and biliary system', 0.5172413793103449, 5.05060299610679, 1.6162861318637973, 'HP:0025031', 'Abnormality of the digestive system'),
(136662, 'HP:0034477', 'Perihepatic adhesions', 'XPO:0107308', 'abnormal anterior hindgut endoderm', 0.42857142857142855, 5.05060299610679, 1.471238981671103, 'HP:0025031', 'Abnormality of the digestive system'),
(136663, 'HP:0034477', 'Perihepatic adhesions', 'XPO:0100214', 'abnormal second pancreatic bud', 0.42857142857142855, 5.05060299610679, 1.471238981671103, 'HP:0025031', 'Abnormality of the digestive system'),
(136664, 'HP:0034477', 'Perihepatic adhesions', 'XPO:0101784', 'abnormal alimentary system morphology', 0.43243243243243246, 5.05060299610679, 1.4778513250178418, 'HP:0025031', 'Abnormality of the digestive system'),
(136665, 'HP:0000662', 'Nyctalopia', 'XPO:0100881', 'abnormal sclera', 0.40384615384615385, 6.02624522851634, 1.560024345217106, 'HP:0000478', 'Abnormality of the eye'),
(136666, 'HP:0000662', 'Nyctalopia', 'XPO:0100918', 'abnormal lens', 0.40384615384615385, 6.02624522851634, 1.560024345217106, 'HP:0000478', 'Abnormality of the eye'),
(136667, 'HP:0000662', 'Nyctalopia', 'XPO:0100485', 'abnormal retina', 0.40384615384615385, 6.02624522851634, 1.560024345217106, 'HP:0000478', 'Abnormality of the eye'),
(136668, 'HP:0000662', 'Nyctalopia', 'XPO:0101173', 'abnormal retinal layer', 0.4375, 6.02624522851634, 1.6237248188889333, 'HP:0000478', 'Abnormality of the eye'),
(136669, 'HP:0100244', 'Fibrosarcoma', 'XPO:0100337', 'abnormal zygote', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(136670, 'HP:0100244', 'Fibrosarcoma', 'XPO:0100549', 'abnormal mitotic cell', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(136671, 'HP:0100244', 'Fibrosarcoma', 'XPO:0100344', 'abnormal portion of organism substance', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(136672, 'HP:0100244', 'Fibrosarcoma', 'XPO:0100852', 'abnormal interdigital region', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(136673, 'HP:0100244', 'Fibrosarcoma', 'XPO:0100899', 'abnormal secondary spermatogonium', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(136674, 'HP:0100244', 'Fibrosarcoma', 'XPO:0100721', 'abnormal centromere', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(136675, 'HP:0100244', 'Fibrosarcoma', 'XPO:0141776', 'abnormal metabolic process', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(136676, 'HP:0100244', 'Fibrosarcoma', 'XPO:0100225', 'abnormal endocrine system', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(136677, 'HP:0100244', 'Fibrosarcoma', 'XPO:0116434', 'abnormal biological process', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(136678, 'HP:0100244', 'Fibrosarcoma', 'XPO:0141271', 'increased surface breathing', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(136679, 'HP:0100244', 'Fibrosarcoma', 'XPO:0100437', 'abnormal proepicardium', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(136680, 'HP:0100244', 'Fibrosarcoma', 'XPO:0100025', 'abnormal oocyte', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(136681, 'HP:0100244', 'Fibrosarcoma', 'XPO:0141263', 'abnormal visually guided collision avoidance behavior', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(136682, 'HP:0100244', 'Fibrosarcoma', 'XPO:0131667', 'abnormal actin cytoskeleton', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(136683, 'HP:0100244', 'Fibrosarcoma', 'XPO:0107312', 'abnormal filopodium', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(136684, 'HP:0100244', 'Fibrosarcoma', 'XPO:0101326', 'abnormal cementoblast', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(136685, 'HP:0100244', 'Fibrosarcoma', 'XPO:0100715', 'abnormal ciliated cell', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(136686, 'HP:0100244', 'Fibrosarcoma', 'XPO:0141264', 'abnormal schooling behavior', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(136687, 'HP:0100244', 'Fibrosarcoma', 'XPO:0100691', 'abnormal keratin accumulating cell', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(136688, 'HP:0100244', 'Fibrosarcoma', 'XPO:0100888', 'abnormal microtubule', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(136689, 'HP:0100244', 'Fibrosarcoma', 'XPO:0100754', 'abnormal electrically active cell', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(136690, 'HP:0100244', 'Fibrosarcoma', 'XPO:0141904', 'abnormal glucosamine metabolic process', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(136691, 'HP:0100244', 'Fibrosarcoma', 'XPO:0131723', 'abnormal pathway-restricted SMAD protein phosphorylation', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(136692, 'HP:0100244', 'Fibrosarcoma', 'XPO:0100372', 'abnormal hematological system', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(136693, 'HP:0100244', 'Fibrosarcoma', 'XPO:0141272', 'absent surface breathing', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(136694, 'HP:0100244', 'Fibrosarcoma', 'XPO:0100232', 'abnormal lymphatic system', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(136695, 'HP:0100244', 'Fibrosarcoma', 'XPO:0101132', 'abnormal apoptotic cell', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(136696, 'HP:0100244', 'Fibrosarcoma', 'XPO:0100317', 'abnormal respiratory system', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(136697, 'HP:0100244', 'Fibrosarcoma', 'XPO:0107288', 'abnormal larval alimentary system', 0.4230769230769231, 4.96264005835567, 1.4489922312515684, 'HP:0002664', 'Neoplasm'),
(136698, 'HP:0100244', 'Fibrosarcoma', 'XPO:0100258', 'abnormal organ part', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(136699, 'HP:0100244', 'Fibrosarcoma', 'XPO:0100285', 'abnormal progenitor cell', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(136700, 'HP:0100244', 'Fibrosarcoma', 'XPO:0141792', 'abnormal small molecule metabolic process', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(136701, 'HP:0100244', 'Fibrosarcoma', 'XPO:0141276', 'decreased surface breathing', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(136702, 'HP:0100244', 'Fibrosarcoma', 'XPO:0141771', 'abnormal urea homeostasis', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(136703, 'HP:0100244', 'Fibrosarcoma', 'XPO:0100501', 'abnormal urogenital system', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(136704, 'HP:0100244', 'Fibrosarcoma', 'XPO:0141860', 'abnormal malate-aspartate shuttle', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(136705, 'HP:0100244', 'Fibrosarcoma', 'XPO:0101333', 'abnormal barrier epithelial cell', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(136706, 'HP:0100244', 'Fibrosarcoma', 'XPO:0141797', 'abnormal hydrogen metabolic process', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(136707, 'HP:0100244', 'Fibrosarcoma', 'XPO:0141775', 'abnormal nitrogen compound metabolic process', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(136708, 'HP:0100244', 'Fibrosarcoma', 'XPO:0141794', 'abnormal prosthetic group metabolic process', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(136709, 'HP:0100244', 'Fibrosarcoma', 'XPO:0141772', 'abnormal water homeostasis', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(136710, 'HP:0100244', 'Fibrosarcoma', 'XPO:0100653', 'abnormal myoblast', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(136711, 'HP:0100244', 'Fibrosarcoma', 'XPO:0141743', 'abnormal chemical homeostasis within a tissue', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(136712, 'HP:0100244', 'Fibrosarcoma', 'XPO:0141778', 'abnormal biosynthetic process', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(136713, 'HP:0100244', 'Fibrosarcoma', 'XPO:0141265', 'abnormal escape behavior', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(136714, 'HP:0100244', 'Fibrosarcoma', 'XPO:0101071', 'abnormal endoplasmic reticulum', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(136715, 'HP:0100244', 'Fibrosarcoma', 'XPO:0100969', 'abnormal disaggregated/reaggregated ectoderm treated with activin', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(136716, 'HP:0100244', 'Fibrosarcoma', 'XPO:0100533', 'abnormal melanoblast', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(136717, 'HP:0100244', 'Fibrosarcoma', 'XPO:0101237', 'abnormal mucus secreting cell', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(136718, 'HP:0100244', 'Fibrosarcoma', 'XPO:0100902', 'abnormal spermatocyte', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(136719, 'HP:0100244', 'Fibrosarcoma', 'XPO:0131666', 'abnormal adherens junction', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(136720, 'HP:0100244', 'Fibrosarcoma', 'XPO:0101467', 'abnormal alkali secreting cell', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(136721, 'HP:0100244', 'Fibrosarcoma', 'XPO:0100481', 'abnormal anatomical line', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(136722, 'HP:0100244', 'Fibrosarcoma', 'XPO:0100626', 'abnormal primordial germ cell', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(136723, 'HP:0100244', 'Fibrosarcoma', 'XPO:0141784', 'abnormal cellular hormone metabolic process', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(136724, 'HP:0100244', 'Fibrosarcoma', 'XPO:0101240', 'abnormal ciliated non-epidermal cell', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(136725, 'HP:0100244', 'Fibrosarcoma', 'XPO:0101435', 'abnormal paracrine cell', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(136726, 'HP:0100244', 'Fibrosarcoma', 'XPO:0101241', 'abnormal nucleate erythrocyte', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(136727, 'HP:0100244', 'Fibrosarcoma', 'XPO:0100289', 'abnormal chondroblast', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(136728, 'HP:0100244', 'Fibrosarcoma', 'XPO:0100152', 'abnormal alimentary system', 0.44, 4.96264005835567, 1.4776879324392194, 'HP:0002664', 'Neoplasm'),
(136729, 'HP:0100244', 'Fibrosarcoma', 'XPO:0141266', 'abnormal surface breathing', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(136730, 'HP:0100244', 'Fibrosarcoma', 'XPO:00000000', 'Xenopus phenotype', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(136731, 'HP:0100244', 'Fibrosarcoma', 'XPO:0101535', 'abnormal absorptive cell', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(136732, 'HP:0100244', 'Fibrosarcoma', 'XPO:0141786', 'abnormal pigment metabolic process', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(136733, 'HP:0100244', 'Fibrosarcoma', 'XPO:0100976', 'abnormal multiciliated cell', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(136734, 'HP:0100244', 'Fibrosarcoma', 'XPO:0116494', 'absent biological process', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(136735, 'HP:0100244', 'Fibrosarcoma', 'XPO:0141783', 'abnormal collagen metabolic process', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(136736, 'HP:0100244', 'Fibrosarcoma', 'XPO:0100791', 'abnormal multiciliated cell precursor', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(136737, 'HP:0100244', 'Fibrosarcoma', 'XPO:0107284', 'abnormal migrating myoblast', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(136738, 'HP:0100244', 'Fibrosarcoma', 'XPO:0100515', 'abnormal somatic stem cell', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(136739, 'HP:0100244', 'Fibrosarcoma', 'XPO:0100108', 'abnormal cell part', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(136740, 'HP:0100244', 'Fibrosarcoma', 'XPO:0100006', 'abnormal anatomical structure', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(136741, 'HP:0100244', 'Fibrosarcoma', 'XPO:0141777', 'abnormal catabolic process', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(136742, 'HP:0100244', 'Fibrosarcoma', 'XPO:0101569', 'abnormal activin-induced ectoderm', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(136743, 'HP:0100244', 'Fibrosarcoma', 'XPO:0100004', 'abnormal cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(136744, 'HP:0100244', 'Fibrosarcoma', 'XPO:0100032', 'abnormal nervous system', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(136745, 'HP:0100244', 'Fibrosarcoma', 'XPO:0100674', 'abnormal secondary oogonium', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(136746, 'HP:0100244', 'Fibrosarcoma', 'XPO:0141791', 'abnormal primary metabolic process', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(136747, 'HP:0100244', 'Fibrosarcoma', 'XPO:0141787', 'abnormal hormone metabolic process', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(136748, 'HP:0100244', 'Fibrosarcoma', 'XPO:0100890', 'abnormal pharyngeal cavity', 0.4074074074074074, 4.96264005835567, 1.421905875953408, 'HP:0002664', 'Neoplasm'),
(136749, 'HP:0100244', 'Fibrosarcoma', 'XPO:0107258', 'abnormal anatomical axis', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(136750, 'HP:0100244', 'Fibrosarcoma', 'XPO:0100493', 'abnormal liver and biliary system', 0.4230769230769231, 4.96264005835567, 1.4489922312515684, 'HP:0002664', 'Neoplasm'),
(136751, 'HP:0100244', 'Fibrosarcoma', 'XPO:0141770', 'abnormal urate homeostasis', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(136752, 'HP:0100244', 'Fibrosarcoma', 'XPO:0100894', 'abnormal nucleus', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(136753, 'HP:0100244', 'Fibrosarcoma', 'XPO:0101297', 'abnormal barrier cell', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(136754, 'HP:0100244', 'Fibrosarcoma', 'XPO:0100546', 'abnormal whole organism', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(136755, 'HP:0100244', 'Fibrosarcoma', 'XPO:0100026', 'abnormal germ cell', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(136756, 'HP:0100244', 'Fibrosarcoma', 'XPO:0115391', 'abnormally undifferentiated alimentary system', 0.4230769230769231, 4.96264005835567, 1.4489922312515684, 'HP:0002664', 'Neoplasm'),
(136757, 'HP:0100244', 'Fibrosarcoma', 'XPO:0101264', 'abnormal mitotic spindle', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(136758, 'HP:0100244', 'Fibrosarcoma', 'XPO:0101110', 'abnormal cell-free extract', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(136759, 'HP:0100244', 'Fibrosarcoma', 'XPO:0101547', 'abnormal lampbrush chromosome', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(136760, 'HP:0100244', 'Fibrosarcoma', 'XPO:0100308', 'abnormal early embryonic cell', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(136761, 'HP:0100244', 'Fibrosarcoma', 'XPO:0100429', 'abnormal spermatid', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(136762, 'HP:0100244', 'Fibrosarcoma', 'XPO:0100704', 'abnormal Merkel cell', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(136763, 'HP:0100244', 'Fibrosarcoma', 'XPO:0100477', 'abnormal pericyte', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(136764, 'HP:0100244', 'Fibrosarcoma', 'XPO:0141738', 'abnormal carbon dioxide homeostasis', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(136765, 'HP:0100244', 'Fibrosarcoma', 'XPO:0100956', 'abnormal centrosome', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(136766, 'HP:0100244', 'Fibrosarcoma', 'XPO:0141796', 'abnormal demethylation', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(136767, 'HP:0100244', 'Fibrosarcoma', 'XPO:0131691', 'abnormal molecular function', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(136768, 'HP:0100244', 'Fibrosarcoma', 'XPO:0141267', 'abnormal resting posture', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(136769, 'HP:0100244', 'Fibrosarcoma', 'XPO:0141782', 'abnormal methylation', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(136770, 'HP:0100244', 'Fibrosarcoma', 'XPO:0100638', 'abnormal polar body', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(136771, 'HP:0100244', 'Fibrosarcoma', 'XPO:0142057', 'abnormal desmosome', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(136772, 'HP:0100244', 'Fibrosarcoma', 'XPO:0101061', 'abnormal plasma membrane', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(136773, 'HP:0100244', 'Fibrosarcoma', 'XPO:0101228', 'abnormal mesenchymal stem cell', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(136774, 'HP:0100244', 'Fibrosarcoma', 'XPO:0141748', 'abnormal gas homeostasis', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(136775, 'HP:0100244', 'Fibrosarcoma', 'XPO:0131725', 'abnormal phosphorylation of RNA polymerase II C-terminal domain', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(136776, 'HP:0100244', 'Fibrosarcoma', 'XPO:0101004', 'abnormal acid secreting cell', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(136777, 'HP:0100244', 'Fibrosarcoma', 'XPO:0100581', 'abnormal immune system', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(136778, 'HP:0100244', 'Fibrosarcoma', 'XPO:0100081', 'abnormal anatomical entity in vitro', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(136779, 'HP:0100244', 'Fibrosarcoma', 'XPO:0141781', 'abnormal secondary metabolic process', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(136780, 'HP:0100244', 'Fibrosarcoma', 'XPO:0100907', 'abnormal cytoplasm', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(136781, 'HP:0100244', 'Fibrosarcoma', 'XPO:0142054', 'abnormal digestive tract', 0.4074074074074074, 4.96264005835567, 1.421905875953408, 'HP:0002664', 'Neoplasm'),
(136782, 'HP:0100244', 'Fibrosarcoma', 'XPO:0101448', 'abnormal myelin accumulating cell', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(136783, 'HP:0100244', 'Fibrosarcoma', 'XPO:0100724', 'abnormal kinetochore', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(136784, 'HP:0100244', 'Fibrosarcoma', 'XPO:0100172', 'abnormal stem cell', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(136785, 'HP:0100244', 'Fibrosarcoma', 'XPO:0101141', 'abnormal Keller explant', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(136786, 'HP:0100244', 'Fibrosarcoma', 'XPO:0141745', 'abnormal creatinine homeostasis', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(136787, 'HP:0100244', 'Fibrosarcoma', 'XPO:0100802', 'abnormal exocrine cell', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(136788, 'HP:0100244', 'Fibrosarcoma', 'XPO:0101373', 'abnormal oxygen accumulating cell', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(136789, 'HP:0100244', 'Fibrosarcoma', 'XPO:0101513', 'abnormal basal body', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(136790, 'HP:0100244', 'Fibrosarcoma', 'XPO:0141790', 'abnormal cellular metabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(136791, 'HP:0034620', 'Elevated circulating membrane cofactor protein concentration', 'XPO:0141873', 'abnormal tricarboxylic acid metabolic process', 0.42592592592592593, 7.41682187759612, 1.7773622944247445, 'HP:0430071', 'Abnormal circulating organic compound concentration'),
(136792, 'HP:0030980', 'Reduced brain glutamine level by MRS', 'XPO:0142051', 'abnormal cerebrospinal fluid', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(136793, 'HP:0030980', 'Reduced brain glutamine level by MRS', 'XPO:0100273', 'abnormal visual system', 0.43333333333333335, 3.94131651835137, 1.3068679445984308, 'UPHENO:0004523', 'abnormal nervous system'),
(136794, 'HP:0030980', 'Reduced brain glutamine level by MRS', 'XPO:0100858', 'abnormal presumptive midbrain-hindbrain boundary', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(136795, 'HP:0030980', 'Reduced brain glutamine level by MRS', 'XPO:0100537', 'abnormal medium cavity', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(136796, 'HP:0030980', 'Reduced brain glutamine level by MRS', 'XPO:0100274', 'abnormal sensory system', 0.4482758620689655, 3.94131651835137, 1.3292091859262085, 'UPHENO:0004523', 'abnormal nervous system'),
(136797, 'HP:0030980', 'Reduced brain glutamine level by MRS', 'XPO:0100916', 'abnormal principal cavity', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(136798, 'HP:0030980', 'Reduced brain glutamine level by MRS', 'XPO:0100164', 'abnormal neural nucleus', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(136799, 'HP:0030980', 'Reduced brain glutamine level by MRS', 'XPO:0100031', 'abnormal central nervous system', 0.4482758620689655, 3.94131651835137, 1.3292091859262085, 'UPHENO:0004523', 'abnormal nervous system'),
(136800, 'HP:0030980', 'Reduced brain glutamine level by MRS', 'XPO:0100175', 'abnormal migrating neuroblast', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(136801, 'HP:0030980', 'Reduced brain glutamine level by MRS', 'XPO:0107253', 'abnormal enteric nervous system', 0.4482758620689655, 3.94131651835137, 1.3292091859262085, 'UPHENO:0004523', 'abnormal nervous system'),
(136802, 'HP:0030980', 'Reduced brain glutamine level by MRS', 'XPO:0101501', 'abnormal parabrachial area', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(136803, 'HP:0030980', 'Reduced brain glutamine level by MRS', 'XPO:0100642', 'abnormal gustatory system', 0.43333333333333335, 3.94131651835137, 1.3068679445984308, 'UPHENO:0004523', 'abnormal nervous system'),
(136804, 'HP:0030980', 'Reduced brain glutamine level by MRS', 'XPO:0100196', 'abnormal neuron', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(136805, 'HP:0030980', 'Reduced brain glutamine level by MRS', 'XPO:0100032', 'abnormal nervous system', 0.4642857142857143, 3.94131651835137, 1.3527368387638634, 'UPHENO:0004523', 'abnormal nervous system'),
(136806, 'HP:0030980', 'Reduced brain glutamine level by MRS', 'XPO:0100702', 'abnormal glial cell', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(136807, 'HP:0030980', 'Reduced brain glutamine level by MRS', 'XPO:0100427', 'abnormal olfactory system', 0.43333333333333335, 3.94131651835137, 1.3068679445984308, 'UPHENO:0004523', 'abnormal nervous system'),
(136808, 'HP:0030980', 'Reduced brain glutamine level by MRS', 'XPO:0100114', 'abnormal peripheral nervous system', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(136809, 'HP:0030980', 'Reduced brain glutamine level by MRS', 'XPO:0100158', 'abnormal neuromere', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(136810, 'HP:0030980', 'Reduced brain glutamine level by MRS', 'XPO:0100587', 'abnormal vestibuloauditory system', 0.43333333333333335, 3.94131651835137, 1.3068679445984308, 'UPHENO:0004523', 'abnormal nervous system'),
(136811, 'HP:0007656', 'Lacrimal gland aplasia', 'XPO:0102657', 'abnormal conjunctiva morphology', 0.4050632911392405, 9.645995805453706, 1.976673672428605, 'UPHENO:0087232', 'abnormal ocular surface region morphology'),
(136812, 'HP:0025124', 'Fragile teeth', 'XPO:0102551', 'abnormal branchial arch skeleton 1 morphology', 0.4050632911392405, 5.725717590856133, 1.5229175983900207, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(136813, 'HP:0025124', 'Fragile teeth', 'XPO:0100027', 'abnormal lower jaw', 0.43333333333333335, 7.0866363731414825, 1.752391440773049, 'HP:0000153', 'Abnormality of the mouth'),
(136814, 'HP:0025124', 'Fragile teeth', 'XPO:0103352', 'decreased size of the mouth', 0.4861111111111111, 7.884497199543557, 1.9577389239177327, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(136815, 'HP:0025124', 'Fragile teeth', 'XPO:0128880', 'decreased size of the lower jaw', 0.475, 7.312692920701687, 1.8637406303810895, 'UPHENO:0076800', 'abnormal mouth morphology'),
(136816, 'HP:0025124', 'Fragile teeth', 'XPO:0131611', 'increased size of the roof of mouth', 0.4520547945205479, 7.312692920701687, 1.8181688303509294, 'UPHENO:0076800', 'abnormal mouth morphology'),
(136817, 'HP:0025124', 'Fragile teeth', 'XPO:0102223', 'abnormal pharyngeal arch morphology', 0.42857142857142855, 5.725717590856133, 1.5664861849086864, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(136818, 'HP:0025124', 'Fragile teeth', 'XPO:0101506', 'abnormal upper jaw', 0.43333333333333335, 7.0866363731414825, 1.752391440773049, 'HP:0000153', 'Abnormality of the mouth'),
(136819, 'HP:0025124', 'Fragile teeth', 'XPO:0103176', 'abnormal fenestra basicranialis morphology', 0.40625, 4.638757693672553, 1.3727692133255593, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(136820, 'HP:0025124', 'Fragile teeth', 'XPO:0102890', 'abnormal dentine morphology', 0.5421686746987951, 9.872199840740173, 2.3135249088816305, 'HP:0006482', 'Abnormal dental morphology'),
(136821, 'HP:0025124', 'Fragile teeth', 'XPO:0140639', 'abnormally necrotic upper jaw', 0.475, 7.312692920701687, 1.8637406303810895, 'UPHENO:0076800', 'abnormal mouth morphology'),
(136822, 'HP:0025124', 'Fragile teeth', 'XPO:0100420', 'abnormal choana', 0.4126984126984127, 5.0624614801082695, 1.445430668412546, 'UPHENO:0002910', 'abnormal face'),
(136823, 'HP:0025124', 'Fragile teeth', 'XPO:0102776', 'abnormal fenestra subocularis morphology', 0.40625, 4.638757693672553, 1.3727692133255593, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(136824, 'HP:0025124', 'Fragile teeth', 'XPO:0141006', 'abnormally necrotic cementum', 0.5056179775280899, 9.872199840740173, 2.2341803233463895, 'HP:0006482', 'Abnormal dental morphology'),
(136825, 'HP:0025124', 'Fragile teeth', 'XPO:0141311', 'abnormal roof of mouth morphology', 0.5, 7.312692920701687, 1.9121575406725366, 'UPHENO:0076800', 'abnormal mouth morphology'),
(136826, 'HP:0025124', 'Fragile teeth', 'XPO:0102525', 'abnormal hyoid arch morphology', 0.4090909090909091, 5.725717590856133, 1.5304701939081158, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(136827, 'HP:0025124', 'Fragile teeth', 'XPO:0102823', 'abnormal palatoquadrate morphology', 0.4266666666666667, 5.725717590856133, 1.5630012280114445, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(136828, 'HP:0025124', 'Fragile teeth', 'XPO:0115558', 'abnormally incomplete structure of mouth', 0.515625, 7.312692920701687, 1.9418051620172418, 'UPHENO:0076800', 'abnormal mouth morphology'),
(136829, 'HP:0025124', 'Fragile teeth', 'XPO:0130701', 'increased size of the upper jaw', 0.4634146341463415, 7.312692920701687, 1.8408717811057655, 'UPHENO:0076800', 'abnormal mouth morphology'),
(136830, 'HP:0025124', 'Fragile teeth', 'XPO:0140789', 'abnormally necrotic roof of mouth', 0.4647887323943662, 7.312692920701687, 1.8435990000545652, 'UPHENO:0076800', 'abnormal mouth morphology'),
(136831, 'HP:0025124', 'Fragile teeth', 'XPO:0103735', 'increased size of the mouth', 0.4861111111111111, 7.884497199543557, 1.9577389239177327, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(136832, 'HP:0025124', 'Fragile teeth', 'XPO:0102103', 'abnormal mandibular arch morphology', 0.4383561643835616, 5.725717590856133, 1.584267528377446, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(136833, 'HP:0025124', 'Fragile teeth', 'XPO:0102563', 'abnormal hyoid arch skeleton morphology', 0.42105263157894735, 5.725717590856133, 1.5526842754751673, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(136834, 'HP:0025124', 'Fragile teeth', 'XPO:0102926', 'abnormal branchial arch skeleton 2 morphology', 0.4050632911392405, 5.725717590856133, 1.5229175983900207, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(136835, 'HP:0025124', 'Fragile teeth', 'XPO:0129585', 'increased size of the tongue', 0.45, 7.884497199543557, 1.8836198501275678, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(136836, 'HP:0025124', 'Fragile teeth', 'XPO:0129152', 'decreased size of the oral cavity', 0.5147058823529411, 7.884497199543557, 2.0144967331818533, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(136837, 'HP:0025124', 'Fragile teeth', 'XPO:0131573', 'decreased size of the roof of mouth', 0.4520547945205479, 7.312692920701687, 1.8181688303509294, 'UPHENO:0076800', 'abnormal mouth morphology'),
(136838, 'HP:0025124', 'Fragile teeth', 'XPO:0140626', 'abnormally necrotic tongue', 0.5147058823529411, 7.884497199543557, 2.0144967331818533, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(136839, 'HP:0025124', 'Fragile teeth', 'XPO:0127750', 'abnormally localised tongue', 0.4925373134328358, 7.884497199543557, 1.970636716503552, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(136840, 'HP:0025124', 'Fragile teeth', 'XPO:0139862', 'abnormally necrotic mandibular arch', 0.4050632911392405, 5.725717590856133, 1.5229175983900207, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(136841, 'HP:0025124', 'Fragile teeth', 'XPO:0128653', 'decreased size of the oral epithelium', 0.4074074074074074, 7.312692920701687, 1.7260490329042149, 'UPHENO:0076800', 'abnormal mouth morphology'),
(136842, 'HP:0025124', 'Fragile teeth', 'XPO:0102735', 'abnormal pharyngeal mesenchyme morphology', 0.40298507462686567, 5.725717590856133, 1.5190058362769763, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(136843, 'HP:0025124', 'Fragile teeth', 'XPO:0140890', 'abnormally necrotic dentine', 0.4891304347826087, 9.872199840740173, 2.197451569514569, 'HP:0006482', 'Abnormal dental morphology'),
(136844, 'HP:0025124', 'Fragile teeth', 'XPO:0102985', 'abnormal branchial arch skeleton 3 morphology', 0.41025641025641024, 5.725717590856133, 1.5326488002692003, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(136845, 'HP:0025124', 'Fragile teeth', 'XPO:0101816', 'abnormal tooth morphology', 0.625, 9.872199840740173, 2.4839736110640565, 'HP:0006482', 'Abnormal dental morphology'),
(136846, 'HP:0025124', 'Fragile teeth', 'XPO:0102552', 'abnormal branchial arch skeleton morphology', 0.4266666666666667, 5.725717590856133, 1.5630012280114445, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(136847, 'HP:0025124', 'Fragile teeth', 'XPO:0141009', 'abnormally necrotic oral epithelium', 0.4177215189873418, 7.312692920701687, 1.7477611949930372, 'UPHENO:0076800', 'abnormal mouth morphology'),
(136848, 'HP:0025124', 'Fragile teeth', 'XPO:0140897', 'abnormally necrotic lower jaw', 0.48717948717948717, 7.312692920701687, 1.8874835064202586, 'UPHENO:0076800', 'abnormal mouth morphology'),
(136849, 'HP:0025124', 'Fragile teeth', 'XPO:0129225', 'decreased size of the upper jaw', 0.4634146341463415, 7.312692920701687, 1.8408717811057655, 'UPHENO:0076800', 'abnormal mouth morphology'),
(136850, 'HP:0025124', 'Fragile teeth', 'XPO:0130358', 'increased size of the lower jaw', 0.475, 7.312692920701687, 1.8637406303810895, 'UPHENO:0076800', 'abnormal mouth morphology'),
(136851, 'HP:0025124', 'Fragile teeth', 'XPO:0101567', 'abnormal tongue', 0.5614035087719298, 7.884497199543557, 2.103897429231332, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(136852, 'HP:0025124', 'Fragile teeth', 'XPO:0102445', 'abnormal branchial arch 3 morphology', 0.40298507462686567, 5.725717590856133, 1.5190058362769763, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(136853, 'HP:0025124', 'Fragile teeth', 'XPO:0139736', 'abnormally necrotic tooth', 0.5625, 9.872199840740173, 2.356504277614693, 'HP:0006482', 'Abnormal dental morphology'),
(136854, 'HP:0025124', 'Fragile teeth', 'XPO:0103828', 'decreased width of the mouth', 0.45454545454545453, 7.884497199543557, 1.8931091789510952, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(136855, 'HP:0025124', 'Fragile teeth', 'XPO:0103224', 'abnormal ventral hyoid arch skeleton morphology', 0.41025641025641024, 5.725717590856133, 1.5326488002692003, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(136856, 'HP:0025124', 'Fragile teeth', 'XPO:0130923', 'increased size of the dentine', 0.4787234042553192, 9.872199840740173, 2.1739487379531184, 'HP:0006482', 'Abnormal dental morphology'),
(136857, 'HP:0025124', 'Fragile teeth', 'XPO:0129449', 'decreased size of the dentine', 0.4787234042553192, 9.872199840740173, 2.1739487379531184, 'HP:0006482', 'Abnormal dental morphology'),
(136858, 'HP:0025124', 'Fragile teeth', 'XPO:0128510', 'decreased size of the cementum', 0.4945054945054945, 9.872199840740173, 2.209492490166528, 'HP:0006482', 'Abnormal dental morphology'),
(136859, 'HP:0025124', 'Fragile teeth', 'XPO:0102861', 'abnormal cementum morphology', 0.5555555555555556, 9.872199840740173, 2.34191277956244, 'HP:0006482', 'Abnormal dental morphology'),
(136860, 'HP:0025124', 'Fragile teeth', 'XPO:0126089', 'absent tongue', 0.4782608695652174, 7.884497199543557, 1.9418667530853457, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(136861, 'HP:0025124', 'Fragile teeth', 'XPO:0141830', 'increased width of mouth', 0.45454545454545453, 7.884497199543557, 1.8931091789510952, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(136862, 'HP:0025124', 'Fragile teeth', 'XPO:0101659', 'abnormal lower jaw morphology', 0.5205479452054794, 7.312692920701687, 1.951052862889655, 'UPHENO:0076800', 'abnormal mouth morphology'),
(136863, 'HP:0025124', 'Fragile teeth', 'XPO:0130132', 'increased size of the oral epithelium', 0.4074074074074074, 7.312692920701687, 1.7260490329042149, 'UPHENO:0076800', 'abnormal mouth morphology'),
(136864, 'HP:0025124', 'Fragile teeth', 'XPO:0103096', 'abnormal oral cavity morphology', 0.5555555555555556, 7.884497199543557, 2.0929109445861864, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(136865, 'HP:0025124', 'Fragile teeth', 'XPO:0128105', 'decreased size of the tongue', 0.4605263157894737, 7.884497199543557, 1.9055231426456665, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(136866, 'HP:0025124', 'Fragile teeth', 'XPO:0102960', 'abnormal oral epithelium morphology', 0.4583333333333333, 7.312692920701687, 1.830751463740579, 'UPHENO:0076800', 'abnormal mouth morphology'),
(136867, 'HP:0025124', 'Fragile teeth', 'XPO:0102690', 'abnormal dorsal hyoid arch skeleton morphology', 0.41025641025641024, 5.725717590856133, 1.5326488002692003, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(136868, 'HP:0025124', 'Fragile teeth', 'XPO:0129990', 'increased size of the cementum', 0.4945054945054945, 9.872199840740173, 2.209492490166528, 'HP:0006482', 'Abnormal dental morphology'),
(136869, 'HP:0025124', 'Fragile teeth', 'XPO:0102899', 'abnormal branchial arch skeleton 4 morphology', 0.4050632911392405, 5.725717590856133, 1.5229175983900207, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(136870, 'HP:0025124', 'Fragile teeth', 'XPO:0102204', 'abnormal branchial arch morphology', 0.4153846153846154, 5.725717590856133, 1.5421981063659433, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(136871, 'HP:0025124', 'Fragile teeth', 'XPO:0115393', 'abnormally decreased volume of oral cavity', 0.5, 7.884497199543557, 1.9855096574360394, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(136872, 'HP:0025124', 'Fragile teeth', 'XPO:0101764', 'abnormal cranium morphology', 0.4126984126984127, 4.638757693672553, 1.3836213127410304, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(136873, 'HP:0025124', 'Fragile teeth', 'XPO:0130628', 'increased size of the oral cavity', 0.5147058823529411, 7.884497199543557, 2.0144967331818533, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(136874, 'HP:0025124', 'Fragile teeth', 'XPO:0130466', 'increased size of the tooth', 0.5357142857142857, 9.872199840740173, 2.2997126964277097, 'HP:0006482', 'Abnormal dental morphology'),
(136875, 'HP:0025124', 'Fragile teeth', 'XPO:0102279', 'abnormal mouth morphology', 0.5238095238095238, 7.312692920701687, 1.9571556393291838, 'UPHENO:0076800', 'abnormal mouth morphology'),
(136876, 'HP:0025124', 'Fragile teeth', 'XPO:0128989', 'decreased size of the tooth', 0.5357142857142857, 9.872199840740173, 2.2997126964277097, 'HP:0006482', 'Abnormal dental morphology'),
(136877, 'HP:0025124', 'Fragile teeth', 'XPO:0103199', 'abnormal tongue morphology', 0.5555555555555556, 7.884497199543557, 2.0929109445861864, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(136878, 'HP:0025124', 'Fragile teeth', 'XPO:0126046', 'absent tooth', 0.4175824175824176, 9.181382707377857, 1.9580561758275088, 'UPHENO:0002826', 'abnormal dentition'),
(136879, 'HP:0025124', 'Fragile teeth', 'XPO:0103138', 'abnormal upper jaw morphology', 0.5066666666666667, 7.312692920701687, 1.9248630461642862, 'UPHENO:0076800', 'abnormal mouth morphology'),
(136880, 'HP:0025124', 'Fragile teeth', 'XPO:0102092', 'abnormal ethmoid region morphology', 0.40625, 4.638757693672553, 1.3727692133255593, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(136881, 'HP:0003419', 'Low back pain', 'XPO:0102130', 'abnormal endoskeleton morphology', 0.4444444444444444, 4.638757693672553, 1.4358516936218344, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(136882, 'HP:0003419', 'Low back pain', 'XPO:0128184', 'decreased size of the skeleton', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(136883, 'HP:0003419', 'Low back pain', 'XPO:0103116', 'abnormal bone marrow morphology', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(136884, 'HP:0003419', 'Low back pain', 'XPO:0101680', 'abnormal skeletal element morphology', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(136885, 'HP:0003419', 'Low back pain', 'XPO:0101070', 'abnormal rib', 0.4098360655737705, 8.05344015541032, 1.816752660002781, 'UPHENO:0002813', 'abnormal vertebral column'),
(136886, 'HP:0003419', 'Low back pain', 'XPO:0102980', 'abnormal perichordal tissue morphology', 0.43478260869565216, 4.638757693672553, 1.4201588541997616, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(136887, 'HP:0003419', 'Low back pain', 'XPO:0101446', 'abnormal transverse process', 0.4098360655737705, 8.05344015541032, 1.816752660002781, 'UPHENO:0002813', 'abnormal vertebral column'),
(136888, 'HP:0003419', 'Low back pain', 'XPO:0107372', 'abnormal flexural organ morphology', 0.47619047619047616, 4.638757693672553, 1.4862477031377266, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(136889, 'HP:0003419', 'Low back pain', 'XPO:0102828', 'abnormal occipital region morphology', 0.4107142857142857, 6.272837960958401, 1.6050994245019483, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(136890, 'HP:0003419', 'Low back pain', 'XPO:0141723', 'abnormal posterior notochord morphology', 0.47619047619047616, 4.638757693672553, 1.4862477031377266, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(136891, 'HP:0003419', 'Low back pain', 'XPO:0125260', 'absent vertebral column', 0.46296296296296297, 8.05344015541032, 1.9309180501496346, 'UPHENO:0002813', 'abnormal vertebral column'),
(136892, 'HP:0003419', 'Low back pain', 'XPO:0128890', 'decreased size of the elastica externa', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(136893, 'HP:0003419', 'Low back pain', 'XPO:0140019', 'abnormally necrotic skeletal system', 0.4444444444444444, 4.638757693672553, 1.4358516936218344, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(136894, 'HP:0003419', 'Low back pain', 'XPO:0140103', 'abnormally necrotic vertebral column', 0.46296296296296297, 8.05344015541032, 1.9309180501496346, 'UPHENO:0002813', 'abnormal vertebral column'),
(136895, 'HP:0003419', 'Low back pain', 'XPO:0103218', 'abnormal joint morphology', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(136896, 'HP:0003419', 'Low back pain', 'XPO:0130368', 'increased size of the elastica externa', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(136897, 'HP:0003419', 'Low back pain', 'XPO:0140683', 'abnormally necrotic flexural organ', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(136898, 'HP:0003419', 'Low back pain', 'XPO:0129832', 'increased size of the skeletal system', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(136899, 'HP:0003419', 'Low back pain', 'XPO:0141709', 'increased size of the anterior notochord', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(136900, 'HP:0003419', 'Low back pain', 'XPO:0103152', 'abnormal otic region morphology', 0.40350877192982454, 6.272837960958401, 1.5909573036826314, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(136901, 'HP:0003419', 'Low back pain', 'XPO:0140350', 'abnormally necrotic notochordal sheath', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(136902, 'HP:0003419', 'Low back pain', 'XPO:0100927', 'abnormal sacral vertebra', 0.4166666666666667, 8.05344015541032, 1.8318297040812228, 'UPHENO:0002813', 'abnormal vertebral column'),
(136903, 'HP:0003419', 'Low back pain', 'XPO:0100895', 'abnormal presacral vertebra', 0.4166666666666667, 8.05344015541032, 1.8318297040812228, 'UPHENO:0002813', 'abnormal vertebral column'),
(136904, 'HP:0003419', 'Low back pain', 'XPO:0101976', 'abnormal portion of organism substance morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(136905, 'HP:0003419', 'Low back pain', 'XPO:0141719', 'abnormal anterior notochord morphology', 0.47619047619047616, 4.638757693672553, 1.4862477031377266, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(136906, 'HP:0003419', 'Low back pain', 'XPO:0139998', 'abnormally necrotic axial skeleton', 0.4117647058823529, 6.211345574613551, 1.599253852164941, 'UPHENO:0087089', 'abnormal axial skeleton plus cranial skeleton morphology'),
(136907, 'HP:0003419', 'Low back pain', 'XPO:0102164', 'abnormal mandibular mesenchyme morphology', 0.4117647058823529, 6.211345574613551, 1.599253852164941, 'UPHENO:0087089', 'abnormal axial skeleton plus cranial skeleton morphology'),
(136908, 'HP:0003419', 'Low back pain', 'XPO:0102010', 'abnormal perichondrium morphology', 0.46511627906976744, 4.638757693672553, 1.4688640910537754, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(136909, 'HP:0003419', 'Low back pain', 'XPO:0101858', 'abnormal vertebral element morphology', 0.44642857142857145, 8.05344015541032, 1.8961238840501222, 'UPHENO:0002813', 'abnormal vertebral column'),
(136910, 'HP:0003419', 'Low back pain', 'XPO:0128352', 'decreased size of the skeletal system', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(136911, 'HP:0003419', 'Low back pain', 'XPO:0102272', 'abnormal notochordal sheath morphology', 0.47619047619047616, 4.638757693672553, 1.4862477031377266, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(136912, 'HP:0003419', 'Low back pain', 'XPO:0128306', 'decreased size of the articular system', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(136913, 'HP:0003419', 'Low back pain', 'XPO:0126886', 'abnormally localised vertebral column', 0.49019607843137253, 8.05344015541032, 1.9868982817607654, 'UPHENO:0002813', 'abnormal vertebral column'),
(136914, 'HP:0003419', 'Low back pain', 'XPO:0128580', 'decreased size of the postcranial axial skeleton', 0.42592592592592593, 6.272837960958401, 1.6345532468244968, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(136915, 'HP:0003419', 'Low back pain', 'XPO:0127548', 'abnormally localised vertebral element', 0.423728813559322, 8.05344015541032, 1.8472884566637167, 'UPHENO:0002813', 'abnormal vertebral column'),
(136916, 'HP:0003419', 'Low back pain', 'XPO:0102144', 'abnormal cranial skeleton morphology', 0.45652173913043476, 6.211345574613551, 1.6839282300806968, 'UPHENO:0087089', 'abnormal axial skeleton plus cranial skeleton morphology'),
(136917, 'HP:0003419', 'Low back pain', 'XPO:0130060', 'increased size of the postcranial axial skeleton', 0.42592592592592593, 6.272837960958401, 1.6345532468244968, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(136918, 'HP:0003419', 'Low back pain', 'XPO:0129434', 'decreased size of the notochordal sheath', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(136919, 'HP:0003419', 'Low back pain', 'XPO:0139917', 'abnormally necrotic notochord', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(136920, 'HP:0003419', 'Low back pain', 'XPO:0100584', 'abnormal vertebral column', 0.5952380952380952, 8.05344015541032, 2.1894552697464333, 'UPHENO:0002813', 'abnormal vertebral column'),
(136921, 'HP:0003419', 'Low back pain', 'XPO:0101638', 'abnormal anatomical structure morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(136922, 'HP:0003419', 'Low back pain', 'XPO:0141713', 'increased size of the posterior notochord', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(136923, 'HP:0003419', 'Low back pain', 'XPO:0102514', 'abnormal perichondrial cell morphology', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(136924, 'HP:0003419', 'Low back pain', 'XPO:0101982', 'abnormal appendicular skeleton morphology', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(136925, 'HP:0003419', 'Low back pain', 'XPO:0102325', 'abnormal vertebral centrum morphology', 0.43859649122807015, 8.05344015541032, 1.8794176210938882, 'UPHENO:0002813', 'abnormal vertebral column'),
(136926, 'HP:0003419', 'Low back pain', 'XPO:0126787', 'abnormally localised vertebral centrum', 0.4166666666666667, 8.05344015541032, 1.8318297040812228, 'UPHENO:0002813', 'abnormal vertebral column'),
(136927, 'HP:0003419', 'Low back pain', 'XPO:0102216', 'abnormal vertebral column morphology', 0.5208333333333334, 8.05344015541032, 2.048047870764469, 'UPHENO:0002813', 'abnormal vertebral column'),
(136928, 'HP:0003419', 'Low back pain', 'XPO:0139771', 'abnormally necrotic skeletal subdivision', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(136929, 'HP:0003419', 'Low back pain', 'XPO:0100252', 'abnormal caudal vertebra', 0.4032258064516129, 8.05344015541032, 1.8020418700394085, 'UPHENO:0002813', 'abnormal vertebral column'),
(136930, 'HP:0003419', 'Low back pain', 'XPO:0100226', 'abnormal vertebral element', 0.5208333333333334, 8.05344015541032, 2.048047870764469, 'UPHENO:0002813', 'abnormal vertebral column'),
(136931, 'HP:0003419', 'Low back pain', 'XPO:0102054', 'abnormal notochord morphology', 0.47619047619047616, 4.638757693672553, 1.4862477031377266, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(136932, 'HP:0003419', 'Low back pain', 'XPO:0101713', 'abnormal anatomical entity in vitro morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(136933, 'HP:0003419', 'Low back pain', 'XPO:0141699', 'abnormally necrotic anterior notochord', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(136934, 'HP:0003419', 'Low back pain', 'XPO:0102728', 'abnormal tendon morphology', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(136935, 'HP:0003419', 'Low back pain', 'XPO:0100693', 'abnormal vertebral centrum', 0.5102040816326531, 8.05344015541032, 2.0270416962841815, 'UPHENO:0002813', 'abnormal vertebral column'),
(136936, 'HP:0003419', 'Low back pain', 'XPO:0102217', 'abnormal elastica externa morphology', 0.5, 4.638757693672553, 1.5229507040072823, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(136937, 'HP:0003419', 'Low back pain', 'XPO:0102093', 'abnormal craniofacial skeleton morphology', 0.4375, 6.211345574613551, 1.6484731386629958, 'UPHENO:0087089', 'abnormal axial skeleton plus cranial skeleton morphology'),
(136938, 'HP:0003419', 'Low back pain', 'XPO:0102605', 'abnormal dermal skeleton morphology', 0.4444444444444444, 4.638757693672553, 1.4358516936218344, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(136939, 'HP:0003419', 'Low back pain', 'XPO:0102097', 'abnormal skeletal system morphology', 0.5, 4.638757693672553, 1.5229507040072823, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(136940, 'HP:0003419', 'Low back pain', 'XPO:0141703', 'abnormally necrotic posterior notochord', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(136941, 'HP:0003419', 'Low back pain', 'XPO:0139889', 'abnormally necrotic cranial skeleton', 0.40384615384615385, 6.211345574613551, 1.5838017617482976, 'UPHENO:0087089', 'abnormal axial skeleton plus cranial skeleton morphology'),
(136942, 'HP:0003419', 'Low back pain', 'XPO:0102401', 'abnormal neurocranium morphology', 0.40350877192982454, 6.272837960958401, 1.5909573036826314, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(136943, 'HP:0003419', 'Low back pain', 'XPO:0129664', 'increased size of the skeleton', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(136944, 'HP:0003419', 'Low back pain', 'XPO:0101226', 'abnormal postsacral vertebra', 0.4166666666666667, 8.05344015541032, 1.8318297040812228, 'UPHENO:0002813', 'abnormal vertebral column'),
(136945, 'HP:0003419', 'Low back pain', 'XPO:0130908', 'increased size of the notochordal sheath', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(136946, 'HP:0003419', 'Low back pain', 'XPO:0139774', 'abnormally necrotic elastica externa', 0.4444444444444444, 4.638757693672553, 1.4358516936218344, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(136947, 'HP:0003419', 'Low back pain', 'XPO:0141708', 'decreased size of the posterior notochord', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(136948, 'HP:0003419', 'Low back pain', 'XPO:0102806', 'abnormal articular system morphology', 0.4878048780487805, 4.638757693672553, 1.5042634845863214, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(136949, 'HP:0003419', 'Low back pain', 'XPO:0140043', 'abnormally necrotic perichondrium', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(136950, 'HP:0003419', 'Low back pain', 'XPO:0140510', 'abnormally necrotic postcranial axial skeleton', 0.4423076923076923, 6.272837960958401, 1.6656903922192745, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(136951, 'HP:0003419', 'Low back pain', 'XPO:0101957', 'abnormal axial skeleton morphology', 0.4666666666666667, 6.211345574613551, 1.702535736723214, 'UPHENO:0087089', 'abnormal axial skeleton plus cranial skeleton morphology'),
(136952, 'HP:0003419', 'Low back pain', 'XPO:0102461', 'abnormal postcranial axial skeleton morphology', 0.5, 6.272837960958401, 1.770993783297728, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(136953, 'HP:0003419', 'Low back pain', 'XPO:0141704', 'decreased size of the anterior notochord', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(136954, 'HP:0003419', 'Low back pain', 'XPO:0102351', 'abnormal sphenoid region morphology', 0.40350877192982454, 6.272837960958401, 1.5909573036826314, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(136955, 'HP:0003419', 'Low back pain', 'XPO:0129707', 'increased size of the vertebral column', 0.44642857142857145, 8.05344015541032, 1.8961238840501222, 'UPHENO:0002813', 'abnormal vertebral column'),
(136956, 'HP:0003419', 'Low back pain', 'XPO:0102567', 'abnormal skeleton morphology', 0.47619047619047616, 4.638757693672553, 1.4862477031377266, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(136957, 'HP:0003419', 'Low back pain', 'XPO:0140432', 'abnormally necrotic skeleton', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(136958, 'HP:0003419', 'Low back pain', 'XPO:0130188', 'increased size of the flexural organ', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(136959, 'HP:0003419', 'Low back pain', 'XPO:0128709', 'decreased size of the flexural organ', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(136960, 'HP:0003419', 'Low back pain', 'XPO:0100253', 'abnormal vertebra', 0.423728813559322, 8.05344015541032, 1.8472884566637167, 'UPHENO:0002813', 'abnormal vertebral column'),
(136961, 'HP:0003419', 'Low back pain', 'XPO:0128227', 'decreased size of the vertebral column', 0.44642857142857145, 8.05344015541032, 1.8961238840501222, 'UPHENO:0002813', 'abnormal vertebral column'),
(136962, 'HP:0003419', 'Low back pain', 'XPO:0140559', 'abnormally necrotic articular system', 0.43478260869565216, 4.638757693672553, 1.4201588541997616, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(136963, 'HP:0003419', 'Low back pain', 'XPO:0102542', 'abnormal vacuolated notochordal tissue morphology', 0.43478260869565216, 4.638757693672553, 1.4201588541997616, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(136964, 'HP:0003419', 'Low back pain', 'XPO:0102564', 'abnormal olfactory region morphology', 0.40350877192982454, 6.272837960958401, 1.5909573036826314, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(136965, 'HP:0003419', 'Low back pain', 'XPO:0129786', 'increased size of the articular system', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(136966, 'HP:0003419', 'Low back pain', 'XPO:0102113', 'abnormal anatomical line morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(136967, 'HP:0003419', 'Low back pain', 'XPO:0101860', 'abnormal skeletal subdivision morphology', 0.46511627906976744, 4.638757693672553, 1.4688640910537754, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(136968, 'HP:0005025', 'Hypoplastic distal humeri', 'XPO:0101248', 'abnormal digit-joint region', 0.4262295081967213, 5.802924133159483, 1.5726975231682194, 'UPHENO:0076727', 'abnormal limb bone morphology'),
(136969, 'HP:0005025', 'Hypoplastic distal humeri', 'XPO:0100298', 'abnormal humerus', 0.4146341463414634, 10.65746099194716, 2.102129215953067, 'HP:0003063', 'Abnormality of the humerus'),
(136970, 'HP:0005025', 'Hypoplastic distal humeri', 'XPO:0100178', 'abnormal digit', 0.4482758620689655, 5.802924133159483, 1.6128579659451951, 'UPHENO:0076727', 'abnormal limb bone morphology'),
(136971, 'HP:0031175', 'Absent cervical vertebra', 'XPO:0125894', 'absent vertebral element', 0.43243243243243246, 12.281312506061912, 2.3045255130848967, 'UPHENO:0026689', 'absent anatomical entity in the vertebral column'),
(136972, 'HP:0031175', 'Absent cervical vertebra', 'XPO:0125260', 'absent vertebral column', 0.4696969696969697, 8.306662838606666, 1.9752504559138773, 'UPHENO:0026023', 'absent anatomical entity in the skeletal system'),
(136973, 'HP:0031175', 'Absent cervical vertebra', 'XPO:0100584', 'abnormal vertebral column', 0.4166666666666667, 8.05344015541032, 1.8318297040812228, 'UPHENO:0002813', 'abnormal vertebral column'),
(136974, 'HP:0031175', 'Absent cervical vertebra', 'XPO:0125788', 'absent postsacral vertebra', 0.48936170212765956, 13.964122330181212, 2.614097678400013, 'HP:0008465', 'Absent vertebra'),
(136975, 'HP:0031175', 'Absent cervical vertebra', 'XPO:0125561', 'absent sacral vertebra', 0.4842105263157895, 13.964122330181212, 2.60030287140462, 'HP:0008465', 'Absent vertebra'),
(136976, 'HP:0031175', 'Absent cervical vertebra', 'XPO:0124805', 'absent vertebra', 0.5, 13.964122330181212, 2.642359015177651, 'HP:0008465', 'Absent vertebra'),
(136977, 'HP:0031175', 'Absent cervical vertebra', 'XPO:0125951', 'absent presacral vertebra', 0.4842105263157895, 13.964122330181212, 2.60030287140462, 'HP:0008465', 'Absent vertebra'),
(136978, 'HP:0031175', 'Absent cervical vertebra', 'XPO:0125164', 'absent vertebral centrum', 0.4266666666666667, 12.281312506061912, 2.289110453703159, 'UPHENO:0026689', 'absent anatomical entity in the vertebral column'),
(136979, 'HP:0031175', 'Absent cervical vertebra', 'XPO:0125551', 'absent cervical vertebra', 0.44660194174757284, 13.964122330181212, 2.4972793491036542, 'HP:0008465', 'Absent vertebra'),
(136980, 'HP:0031175', 'Absent cervical vertebra', 'XPO:0125168', 'absent caudal vertebra', 0.46938775510204084, 13.964122330181212, 2.5601929678315343, 'HP:0008465', 'Absent vertebra'),
(136981, 'HP:0000549', 'Abnormal conjugate eye movement', 'XPO:0101173', 'abnormal retinal layer', 0.41818181818181815, 6.02624522851634, 1.5874716332805665, 'HP:0000478', 'Abnormality of the eye'),
(136982, 'HP:0001543', 'Gastroschisis', 'XPO:0103013', 'abnormal ventral foregut morphology', 0.4318181818181818, 5.05060299610679, 1.476801341705883, 'HP:0025031', 'Abnormality of the digestive system'),
(136983, 'HP:0001543', 'Gastroschisis', 'XPO:0103009', 'abnormal manicotto glandulare morphology', 0.4523809523809524, 5.05060299610679, 1.511554363387861, 'HP:0025031', 'Abnormality of the digestive system'),
(136984, 'HP:0001543', 'Gastroschisis', 'XPO:0101377', 'abnormal manicotto glandulare', 0.4166666666666667, 5.05060299610679, 1.45066119926208, 'HP:0025031', 'Abnormality of the digestive system'),
(136985, 'HP:0001543', 'Gastroschisis', 'XPO:0101740', 'abnormal cell part morphology', 0.4166666666666667, 2.786899518863159, 1.0775936770692605, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(136986, 'HP:0001543', 'Gastroschisis', 'XPO:0142061', 'abnormal digestive tract morphology', 0.4634146341463415, 5.05060299610679, 1.52987690343349, 'HP:0025031', 'Abnormality of the digestive system'),
(136987, 'HP:0001543', 'Gastroschisis', 'XPO:0100621', 'abnormal peritoneum', 0.4594594594594595, 10.854497839006713, 2.2332043591695534, 'HP:0004298', 'Abnormality of the abdominal wall'),
(136988, 'HP:0001543', 'Gastroschisis', 'XPO:0140165', 'abnormally necrotic midgut', 0.40425531914893614, 5.05060299610679, 1.4288922723864537, 'HP:0025031', 'Abnormality of the digestive system'),
(136989, 'HP:0001543', 'Gastroschisis', 'XPO:0141833', 'edematous alimentary system', 0.4634146341463415, 5.05060299610679, 1.52987690343349, 'HP:0025031', 'Abnormality of the digestive system'),
(136990, 'HP:0001543', 'Gastroschisis', 'XPO:0102253', 'abnormal peritoneum morphology', 0.44680851063829785, 10.854497839006713, 2.2022447668624876, 'HP:0004298', 'Abnormality of the abdominal wall'),
(136991, 'HP:0001543', 'Gastroschisis', 'XPO:0102113', 'abnormal anatomical line morphology', 0.43333333333333335, 2.786899518863159, 1.0989342374200721, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(136992, 'HP:0001543', 'Gastroschisis', 'XPO:0142034', 'abnormally necrotic digestive tract', 0.41304347826086957, 5.05060299610679, 1.4443402053625447, 'HP:0025031', 'Abnormality of the digestive system'),
(136993, 'HP:0001543', 'Gastroschisis', 'XPO:0115392', 'abnormally incomplete structure of alimentary system', 0.475, 5.05060299610679, 1.5488823141706813, 'HP:0025031', 'Abnormality of the digestive system'),
(136994, 'HP:0001543', 'Gastroschisis', 'XPO:0140269', 'abnormally necrotic anatomical line', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(136995, 'HP:0001543', 'Gastroschisis', 'XPO:0141834', 'edematous foregut', 0.4222222222222222, 5.05060299610679, 1.4603002501466684, 'HP:0025031', 'Abnormality of the digestive system'),
(136996, 'HP:0001543', 'Gastroschisis', 'XPO:0101381', 'abnormal ventral foregut', 0.40540540540540543, 5.05060299610679, 1.4309233924911664, 'HP:0025031', 'Abnormality of the digestive system'),
(136997, 'HP:0001543', 'Gastroschisis', 'XPO:0139718', 'abnormally necrotic anatomical structure', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(136998, 'HP:0001543', 'Gastroschisis', 'XPO:0107375', 'abnormal larval alimentary system morphology', 0.4634146341463415, 5.05060299610679, 1.52987690343349, 'HP:0025031', 'Abnormality of the digestive system'),
(136999, 'HP:0001543', 'Gastroschisis', 'XPO:0140542', 'abnormally necrotic larval alimentary system', 0.40425531914893614, 5.05060299610679, 1.4288922723864537, 'HP:0025031', 'Abnormality of the digestive system'),
(137000, 'HP:0001543', 'Gastroschisis', 'XPO:0102118', 'abnormal oral evagination morphology', 0.4523809523809524, 5.05060299610679, 1.511554363387861, 'HP:0025031', 'Abnormality of the digestive system'),
(137001, 'HP:0001543', 'Gastroschisis', 'XPO:0115391', 'abnormally undifferentiated alimentary system', 0.4411764705882353, 5.05060299610679, 1.4927180591674907, 'HP:0025031', 'Abnormality of the digestive system'),
(137002, 'HP:0001543', 'Gastroschisis', 'XPO:0139827', 'abnormally necrotic foregut', 0.40425531914893614, 5.05060299610679, 1.4288922723864537, 'HP:0025031', 'Abnormality of the digestive system'),
(137003, 'HP:0001543', 'Gastroschisis', 'XPO:0101101', 'abnormal posterior foregut', 0.40540540540540543, 5.05060299610679, 1.4309233924911664, 'HP:0025031', 'Abnormality of the digestive system'),
(137004, 'HP:0001543', 'Gastroschisis', 'XPO:0102653', 'abnormal dorsal foregut morphology', 0.4318181818181818, 5.05060299610679, 1.476801341705883, 'HP:0025031', 'Abnormality of the digestive system'),
(137005, 'HP:0001543', 'Gastroschisis', 'XPO:0100735', 'abnormal hindgut', 0.4166666666666667, 5.05060299610679, 1.45066119926208, 'HP:0025031', 'Abnormality of the digestive system'),
(137006, 'HP:0001543', 'Gastroschisis', 'XPO:0101890', 'abnormal organ part morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(137007, 'HP:0001543', 'Gastroschisis', 'XPO:0102125', 'abnormal liver and biliary system morphology', 0.4634146341463415, 5.05060299610679, 1.52987690343349, 'HP:0025031', 'Abnormality of the digestive system'),
(137008, 'HP:0001543', 'Gastroschisis', 'XPO:0102618', 'abnormal gut epithelium morphology', 0.4318181818181818, 5.05060299610679, 1.476801341705883, 'HP:0025031', 'Abnormality of the digestive system'),
(137009, 'HP:0001543', 'Gastroschisis', 'XPO:0100523', 'abnormal midgut', 0.4166666666666667, 5.05060299610679, 1.45066119926208, 'HP:0025031', 'Abnormality of the digestive system'),
(137010, 'HP:0001543', 'Gastroschisis', 'XPO:0100986', 'abnormal gut epithelium', 0.40540540540540543, 5.05060299610679, 1.4309233924911664, 'HP:0025031', 'Abnormality of the digestive system'),
(137011, 'HP:0001543', 'Gastroschisis', 'XPO:0101636', 'abnormal cell morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(137012, 'HP:0001543', 'Gastroschisis', 'XPO:0102742', 'abnormal cell-free extract morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(137013, 'HP:0001543', 'Gastroschisis', 'XPO:0102178', 'abnormal whole organism morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(137014, 'HP:0001543', 'Gastroschisis', 'XPO:0129821', 'increased size of the pharyngeal cavity', 0.4318181818181818, 5.05060299610679, 1.476801341705883, 'HP:0025031', 'Abnormality of the digestive system'),
(137015, 'HP:0001543', 'Gastroschisis', 'XPO:0100486', 'abnormal oral evagination', 0.4166666666666667, 5.05060299610679, 1.45066119926208, 'HP:0025031', 'Abnormality of the digestive system'),
(137016, 'HP:0001543', 'Gastroschisis', 'XPO:0101847', 'abnormal first pancreatic bud morphology', 0.40425531914893614, 5.05060299610679, 1.4288922723864537, 'HP:0025031', 'Abnormality of the digestive system'),
(137017, 'HP:0001543', 'Gastroschisis', 'XPO:0102094', 'abnormal anterior foregut morphology', 0.4318181818181818, 5.05060299610679, 1.476801341705883, 'HP:0025031', 'Abnormality of the digestive system'),
(137018, 'HP:0001543', 'Gastroschisis', 'XPO:0139906', 'abnormally necrotic alimentary system', 0.4318181818181818, 5.05060299610679, 1.476801341705883, 'HP:0025031', 'Abnormality of the digestive system'),
(137019, 'HP:0001543', 'Gastroschisis', 'XPO:0107345', 'abnormal anatomical axis morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(137020, 'HP:0001543', 'Gastroschisis', 'XPO:0102367', 'abnormal hindgut morphology', 0.4418604651162791, 5.05060299610679, 1.4938747567910164, 'HP:0025031', 'Abnormality of the digestive system'),
(137021, 'HP:0001543', 'Gastroschisis', 'XPO:0101694', 'abnormal anatomical space morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(137022, 'HP:0001543', 'Gastroschisis', 'XPO:0101638', 'abnormal anatomical structure morphology', 0.43333333333333335, 2.786899518863159, 1.0989342374200721, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(137023, 'HP:0001543', 'Gastroschisis', 'XPO:0100462', 'abnormal anterior foregut', 0.40540540540540543, 5.05060299610679, 1.4309233924911664, 'HP:0025031', 'Abnormality of the digestive system'),
(137024, 'HP:0001543', 'Gastroschisis', 'XPO:0102733', 'abnormal posterior foregut morphology', 0.4318181818181818, 5.05060299610679, 1.476801341705883, 'HP:0025031', 'Abnormality of the digestive system'),
(137025, 'HP:0001543', 'Gastroschisis', 'XPO:0101084', 'abnormal mesentery', 0.425, 10.854497839006713, 2.1478271768412496, 'HP:0004298', 'Abnormality of the abdominal wall'),
(137026, 'HP:0001543', 'Gastroschisis', 'XPO:0101784', 'abnormal alimentary system morphology', 0.48717948717948717, 5.05060299610679, 1.5686140945403009, 'HP:0025031', 'Abnormality of the digestive system'),
(137027, 'HP:0001543', 'Gastroschisis', 'XPO:0100156', 'abnormal foregut', 0.4166666666666667, 5.05060299610679, 1.45066119926208, 'HP:0025031', 'Abnormality of the digestive system'),
(137028, 'HP:0001543', 'Gastroschisis', 'XPO:0133432', 'abnormal cilium morphology in the alimentary system', 0.4222222222222222, 5.05060299610679, 1.4603002501466684, 'HP:0025031', 'Abnormality of the digestive system'),
(137029, 'HP:0001543', 'Gastroschisis', 'XPO:0102830', 'abnormal digestive enzyme secreting cell morphology', 0.41304347826086957, 5.05060299610679, 1.4443402053625447, 'HP:0025031', 'Abnormality of the digestive system'),
(137030, 'HP:0001543', 'Gastroschisis', 'XPO:0107288', 'abnormal larval alimentary system', 0.4411764705882353, 5.05060299610679, 1.4927180591674907, 'HP:0025031', 'Abnormality of the digestive system'),
(137031, 'HP:0001543', 'Gastroschisis', 'XPO:0100152', 'abnormal alimentary system', 0.45454545454545453, 5.05060299610679, 1.5151662069205463, 'HP:0025031', 'Abnormality of the digestive system'),
(137032, 'HP:0001543', 'Gastroschisis', 'XPO:0101021', 'abnormal dorsal foregut', 0.40540540540540543, 5.05060299610679, 1.4309233924911664, 'HP:0025031', 'Abnormality of the digestive system'),
(137033, 'HP:0001543', 'Gastroschisis', 'XPO:0102155', 'abnormal midgut morphology', 0.4418604651162791, 5.05060299610679, 1.4938747567910164, 'HP:0025031', 'Abnormality of the digestive system'),
(137034, 'HP:0001543', 'Gastroschisis', 'XPO:0140201', 'abnormally necrotic hindgut', 0.40425531914893614, 5.05060299610679, 1.4288922723864537, 'HP:0025031', 'Abnormality of the digestive system'),
(137035, 'HP:0001543', 'Gastroschisis', 'XPO:0101976', 'abnormal portion of organism substance morphology', 0.43333333333333335, 2.786899518863159, 1.0989342374200721, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(137036, 'HP:0001543', 'Gastroschisis', 'XPO:0140185', 'abnormally necrotic manicotto glandulare', 0.40425531914893614, 5.05060299610679, 1.4288922723864537, 'HP:0025031', 'Abnormality of the digestive system'),
(137037, 'HP:0001543', 'Gastroschisis', 'XPO:0100890', 'abnormal pharyngeal cavity', 0.42857142857142855, 5.05060299610679, 1.471238981671103, 'HP:0025031', 'Abnormality of the digestive system'),
(137038, 'HP:0001543', 'Gastroschisis', 'XPO:0103711', 'increased size of the alimentary system', 0.41304347826086957, 5.05060299610679, 1.4443402053625447, 'HP:0025031', 'Abnormality of the digestive system'),
(137039, 'HP:0001543', 'Gastroschisis', 'XPO:0103321', 'decreased size of the alimentary system', 0.41304347826086957, 5.05060299610679, 1.4443402053625447, 'HP:0025031', 'Abnormality of the digestive system'),
(137040, 'HP:0001543', 'Gastroschisis', 'XPO:0128341', 'decreased size of the pharyngeal cavity', 0.4318181818181818, 5.05060299610679, 1.476801341705883, 'HP:0025031', 'Abnormality of the digestive system'),
(137041, 'HP:0001543', 'Gastroschisis', 'XPO:0140144', 'abnormally necrotic portion of organism substance', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(137042, 'HP:0001543', 'Gastroschisis', 'XPO:0115494', 'abnormally incomplete closure of proctodeum', 0.44680851063829785, 10.688487887567785, 2.185339185119703, 'UPHENO:0033572', 'abnormal incomplete closing of the anatomical entity'),
(137043, 'HP:0001543', 'Gastroschisis', 'XPO:0140425', 'abnormally necrotic oral evagination', 0.41304347826086957, 5.05060299610679, 1.4443402053625447, 'HP:0025031', 'Abnormality of the digestive system'),
(137044, 'HP:0001543', 'Gastroschisis', 'XPO:0100493', 'abnormal liver and biliary system', 0.4411764705882353, 5.05060299610679, 1.4927180591674907, 'HP:0025031', 'Abnormality of the digestive system'),
(137045, 'HP:0001543', 'Gastroschisis', 'XPO:0102773', 'abnormal Keller explant morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(137046, 'HP:0001543', 'Gastroschisis', 'XPO:0101713', 'abnormal anatomical entity in vitro morphology', 0.43333333333333335, 2.786899518863159, 1.0989342374200721, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(137047, 'HP:0001543', 'Gastroschisis', 'XPO:0142054', 'abnormal digestive tract', 0.42857142857142855, 5.05060299610679, 1.471238981671103, 'HP:0025031', 'Abnormality of the digestive system'),
(137048, 'HP:0001543', 'Gastroschisis', 'XPO:0102522', 'abnormal pharyngeal cavity morphology', 0.48717948717948717, 5.05060299610679, 1.5686140945403009, 'HP:0025031', 'Abnormality of the digestive system'),
(137049, 'HP:0001543', 'Gastroschisis', 'XPO:0102801', 'abnormal hepato-pancreatic duct morphology', 0.41304347826086957, 5.05060299610679, 1.4443402053625447, 'HP:0025031', 'Abnormality of the digestive system'),
(137050, 'HP:0001543', 'Gastroschisis', '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'),
(137051, 'HP:0001543', 'Gastroschisis', 'XPO:0103201', 'abnormal activin-induced ectoderm morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(137052, 'HP:0001543', 'Gastroschisis', 'XPO:0103233', 'abnormal proctodeum morphology', 0.41304347826086957, 5.05060299610679, 1.4443402053625447, 'HP:0025031', 'Abnormality of the digestive system'),
(137053, 'HP:0001543', 'Gastroschisis', 'XPO:0140114', 'abnormally necrotic liver and biliary system', 0.41304347826086957, 5.05060299610679, 1.4443402053625447, 'HP:0025031', 'Abnormality of the digestive system'),
(137054, 'HP:0001543', 'Gastroschisis', 'XPO:0101788', 'abnormal foregut morphology', 0.4418604651162791, 5.05060299610679, 1.4938747567910164, 'HP:0025031', 'Abnormality of the digestive system'),
(137055, 'HP:0001543', 'Gastroschisis', 'XPO:0141316', 'abnormal anatomical region morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(137056, 'HP:0011582', 'Abdominal ectopia cordis', 'XPO:0101770', 'abnormal trunk vasculature morphology', 0.40476190476190477, 5.9590888072311134, 1.5530653998657664, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(137057, 'HP:0011582', 'Abdominal ectopia cordis', 'XPO:0102113', 'abnormal anatomical line morphology', 0.4074074074074074, 2.485033483301678, 1.006191357919822, 'UPHENO:0076692', 'abnormal anatomical entity morphology'),
(137058, 'HP:0011582', 'Abdominal ectopia cordis', 'XPO:0101919', 'abnormal heart primordium morphology', 0.425, 5.9590888072311134, 1.5914184688739863, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(137059, 'HP:0011582', 'Abdominal ectopia cordis', 'XPO:0102532', 'abnormal angioblast morphology', 0.425, 5.9590888072311134, 1.5914184688739863, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(137060, 'HP:0011582', 'Abdominal ectopia cordis', 'XPO:0139811', 'abnormally necrotic circulatory system', 0.4146341463414634, 5.9590888072311134, 1.57189112236161, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(137061, 'HP:0011582', 'Abdominal ectopia cordis', 'XPO:0141328', 'edematous circulatory system', 0.4473684210526316, 5.9590888072311134, 1.6327608981732116, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(137062, 'HP:0011582', 'Abdominal ectopia cordis', 'XPO:0101976', 'abnormal portion of organism substance morphology', 0.4074074074074074, 2.485033483301678, 1.006191357919822, 'UPHENO:0076692', 'abnormal anatomical entity morphology'),
(137063, 'HP:0011582', 'Abdominal ectopia cordis', 'XPO:0102935', 'abnormal bulbous arteriosis morphology', 0.4473684210526316, 5.9590888072311134, 1.6327608981732116, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(137064, 'HP:0011582', 'Abdominal ectopia cordis', 'XPO:0101713', 'abnormal anatomical entity in vitro morphology', 0.4074074074074074, 2.485033483301678, 1.006191357919822, 'UPHENO:0076692', 'abnormal anatomical entity morphology'),
(137065, 'HP:0011582', 'Abdominal ectopia cordis', 'XPO:0100054', 'abnormal blood vessel', 0.4117647058823529, 5.249153838287537, 1.4701755971154233, 'UPHENO:0080362', 'abnormal cardiovascular system'),
(137066, 'HP:0011582', 'Abdominal ectopia cordis', 'XPO:0101900', 'abnormal circulatory system morphology', 0.4857142857142857, 5.9590888072311134, 1.7012979055745219, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(137067, 'HP:0011582', 'Abdominal ectopia cordis', 'XPO:0102800', 'abnormal circulating cell morphology', 0.425, 5.9590888072311134, 1.5914184688739863, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(137068, 'HP:0011582', 'Abdominal ectopia cordis', 'XPO:0101638', 'abnormal anatomical structure morphology', 0.4074074074074074, 2.485033483301678, 1.006191357919822, 'UPHENO:0076692', 'abnormal anatomical entity morphology'),
(137069, 'HP:0011582', 'Abdominal ectopia cordis', 'XPO:0139990', 'abnormally necrotic cardiovascular system', 0.4146341463414634, 5.9590888072311134, 1.57189112236161, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(137070, 'HP:0011582', 'Abdominal ectopia cordis', 'XPO:0101995', 'abnormal cardiovascular system morphology', 0.4857142857142857, 5.9590888072311134, 1.7012979055745219, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(137071, 'HP:0011348', 'Abnormal sixth cranial nerve morphology', 'XPO:0101421', 'abnormal oculomotor nerve', 0.52, 8.429051634704384, 2.093587077254319, 'HP:0045010', 'Abnormal peripheral nerve morphology by anatomical site'),
(137072, 'HP:0011348', 'Abnormal sixth cranial nerve morphology', 'XPO:0101600', 'abnormal Schwann cell', 0.4489795918367347, 8.429051634704384, 1.945371985641907, 'HP:0045010', 'Abnormal peripheral nerve morphology by anatomical site'),
(137073, 'HP:0011348', 'Abnormal sixth cranial nerve morphology', 'XPO:0127299', 'abnormally localised accessory nerve', 0.45454545454545453, 9.57905464648184, 2.0866518033444956, 'UPHENO:0076772', 'abnormal cranial nerve morphology'),
(137074, 'HP:0011348', 'Abnormal sixth cranial nerve morphology', 'XPO:0131555', 'abnormally localised nasociliary nerve', 0.40625, 8.429051634704384, 1.8504870241638163, 'HP:0045010', 'Abnormal peripheral nerve morphology by anatomical site'),
(137075, 'HP:0011348', 'Abnormal sixth cranial nerve morphology', 'XPO:0101596', 'abnormal accessory nerve', 0.5769230769230769, 9.57905464648184, 2.35082489366235, 'UPHENO:0076772', 'abnormal cranial nerve morphology'),
(137076, 'HP:0011348', 'Abnormal sixth cranial nerve morphology', 'XPO:0125408', 'absent abducens nerve', 0.44285714285714284, 13.7526182249875, 2.4678827390949993, 'HP:0011348', 'Abnormal sixth cranial nerve morphology'),
(137077, 'HP:0011348', 'Abnormal sixth cranial nerve morphology', 'XPO:0131652', 'abnormal cephalic nerve', 0.5416666666666666, 8.429051634704384, 2.1367583630657774, 'HP:0045010', 'Abnormal peripheral nerve morphology by anatomical site'),
(137078, 'HP:0011348', 'Abnormal sixth cranial nerve morphology', 'XPO:0139921', 'abnormally necrotic cranial nerve', 0.4166666666666667, 9.57905464648184, 1.9978170009706677, 'UPHENO:0076772', 'abnormal cranial nerve morphology'),
(137079, 'HP:0011348', 'Abnormal sixth cranial nerve morphology', 'XPO:0131671', 'abnormal nasociliary nerve', 0.5098039215686274, 8.429051634704384, 2.0729601005510805, 'HP:0045010', 'Abnormal peripheral nerve morphology by anatomical site'),
(137080, 'HP:0011348', 'Abnormal sixth cranial nerve morphology', 'XPO:0102817', 'abnormal vestibulocochlear nerve morphology', 0.4225352112676056, 9.57905464648184, 2.0118369414033395, 'UPHENO:0076772', 'abnormal cranial nerve morphology'),
(137081, 'HP:0011348', 'Abnormal sixth cranial nerve morphology', 'XPO:0126818', 'abnormally localised cranial nerve', 0.41935483870967744, 8.429051634704384, 1.8800966966480739, 'HP:0045010', 'Abnormal peripheral nerve morphology by anatomical site'),
(137082, 'HP:0011348', 'Abnormal sixth cranial nerve morphology', 'XPO:0103228', 'abnormal accessory nerve morphology', 0.43478260869565216, 9.57905464648184, 2.0407857232045656, 'UPHENO:0076772', 'abnormal cranial nerve morphology'),
(137083, 'HP:0011348', 'Abnormal sixth cranial nerve morphology', 'XPO:0141281', 'abnormal cephalic nerve morphology', 0.45161290322580644, 8.429051634704384, 1.95106854830605, 'HP:0045010', 'Abnormal peripheral nerve morphology by anatomical site'),
(137084, 'HP:0011348', 'Abnormal sixth cranial nerve morphology', 'XPO:0101510', 'abnormal optic nerve', 0.4262295081967213, 8.429051634704384, 1.895444679441956, 'HP:0045010', 'Abnormal peripheral nerve morphology by anatomical site'),
(137085, 'HP:0011348', 'Abnormal sixth cranial nerve morphology', 'XPO:0127303', 'abnormally localised vestibulocochlear ganglion', 0.4411764705882353, 9.57905464648184, 2.0557367342407185, 'UPHENO:0076772', 'abnormal cranial nerve morphology'),
(137086, 'HP:0011348', 'Abnormal sixth cranial nerve morphology', 'XPO:0101879', 'abnormal cranial ganglion morphology', 0.4406779661016949, 7.318748312764234, 1.7958872795582561, 'HP:0000759', 'Abnormal peripheral nervous system morphology'),
(137087, 'HP:0011348', 'Abnormal sixth cranial nerve morphology', 'XPO:0131670', 'abnormal maxillary nerve', 0.5098039215686274, 8.429051634704384, 2.0729601005510805, 'HP:0045010', 'Abnormal peripheral nerve morphology by anatomical site'),
(137088, 'HP:0011348', 'Abnormal sixth cranial nerve morphology', 'XPO:0131679', 'abnormal frontal nerve', 0.5098039215686274, 8.429051634704384, 2.0729601005510805, 'HP:0045010', 'Abnormal peripheral nerve morphology by anatomical site'),
(137089, 'HP:0011348', 'Abnormal sixth cranial nerve morphology', 'XPO:0101312', 'abnormal trigeminal ganglion', 0.41304347826086957, 6.642668884102504, 1.6564151233386355, 'HP:0410008', 'Abnormality of the peripheral nervous system'),
(137090, 'HP:0011348', 'Abnormal sixth cranial nerve morphology', 'XPO:0102944', 'abnormal trigeminal ganglion morphology', 0.40625, 7.318748312764234, 1.7243089926287778, 'HP:0000759', 'Abnormal peripheral nervous system morphology'),
(137091, 'HP:0011348', 'Abnormal sixth cranial nerve morphology', 'XPO:0101742', 'abnormal trigeminal nerve morphology', 0.43478260869565216, 9.57905464648184, 2.0407857232045656, 'UPHENO:0076772', 'abnormal cranial nerve morphology'),
(137092, 'HP:0011348', 'Abnormal sixth cranial nerve morphology', 'XPO:0125241', 'absent vestibulocochlear nerve', 0.410958904109589, 9.57905464648184, 1.9840861372238967, 'UPHENO:0076772', 'abnormal cranial nerve morphology'),
(137093, 'HP:0011348', 'Abnormal sixth cranial nerve morphology', 'XPO:0102366', 'abnormal lateral line system morphology', 0.4166666666666667, 7.318748312764234, 1.7462755978515432, 'HP:0000759', 'Abnormal peripheral nervous system morphology'),
(137094, 'HP:0011348', 'Abnormal sixth cranial nerve morphology', 'XPO:0127648', 'abnormally localised hypoglossal nerve', 0.40540540540540543, 9.57905464648184, 1.9706345506860228, 'UPHENO:0076772', 'abnormal cranial nerve morphology'),
(137095, 'HP:0011348', 'Abnormal sixth cranial nerve morphology', 'XPO:0126417', 'abnormally localised nerve', 0.4074074074074074, 8.429051634704384, 1.853121170727398, 'HP:0045010', 'Abnormal peripheral nerve morphology by anatomical site'),
(137096, 'HP:0011348', 'Abnormal sixth cranial nerve morphology', 'XPO:0101746', 'abnormal peripheral nervous system morphology', 0.43478260869565216, 7.318748312764234, 1.783834208610917, 'HP:0000759', 'Abnormal peripheral nervous system morphology'),
(137097, 'HP:0011348', 'Abnormal sixth cranial nerve morphology', 'XPO:0131554', 'abnormally localised maxillary nerve', 0.40625, 8.429051634704384, 1.8504870241638163, 'HP:0045010', 'Abnormal peripheral nerve morphology by anatomical site'),
(137098, 'HP:0011348', 'Abnormal sixth cranial nerve morphology', 'XPO:0102750', 'abnormal trochlear nerve morphology', 0.44776119402985076, 9.57905464648184, 2.0710212326738464, 'UPHENO:0076772', 'abnormal cranial nerve morphology'),
(137099, 'HP:0011348', 'Abnormal sixth cranial nerve morphology', 'XPO:0141312', 'abnormal maxillary nerve morphology', 0.44776119402985076, 9.57905464648184, 2.0710212326738464, 'UPHENO:0076772', 'abnormal cranial nerve morphology'),
(137100, 'HP:0011348', 'Abnormal sixth cranial nerve morphology', 'XPO:0100635', 'abnormal sympathetic chain', 0.46808510638297873, 8.429051634704384, 1.986331677021293, 'HP:0045010', 'Abnormal peripheral nerve morphology by anatomical site'),
(137101, 'HP:0011348', 'Abnormal sixth cranial nerve morphology', 'XPO:0101118', 'abnormal trochlear nerve', 0.52, 8.429051634704384, 2.093587077254319, 'HP:0045010', 'Abnormal peripheral nerve morphology by anatomical site'),
(137102, 'HP:0011348', 'Abnormal sixth cranial nerve morphology', 'XPO:0100223', 'abnormal facial nerve', 0.4918032786885246, 9.57905464648184, 2.1704862316716764, 'UPHENO:0076772', 'abnormal cranial nerve morphology'),
(137103, 'HP:0011348', 'Abnormal sixth cranial nerve morphology', 'XPO:0141297', 'abnormal frontal nerve morphology', 0.44776119402985076, 9.57905464648184, 2.0710212326738464, 'UPHENO:0076772', 'abnormal cranial nerve morphology'),
(137104, 'HP:0011348', 'Abnormal sixth cranial nerve morphology', 'XPO:0103090', 'abnormal vestibulocochlear ganglion morphology', 0.410958904109589, 9.57905464648184, 1.9840861372238967, 'UPHENO:0076772', 'abnormal cranial nerve morphology'),
(137105, 'HP:0011348', 'Abnormal sixth cranial nerve morphology', 'XPO:0140007', 'abnormally necrotic cephalic nerve', 0.4057971014492754, 8.429051634704384, 1.8494552498855752, 'HP:0045010', 'Abnormal peripheral nerve morphology by anatomical site'),
(137106, 'HP:0011348', 'Abnormal sixth cranial nerve morphology', 'XPO:0101458', 'abnormal vestibulocochlear ganglion', 0.5357142857142857, 9.57905464648184, 2.26531154982226, 'UPHENO:0076772', 'abnormal cranial nerve morphology'),
(137107, 'HP:0011348', 'Abnormal sixth cranial nerve morphology', 'XPO:0100739', 'abnormal hypoglossal nerve', 0.5, 9.57905464648184, 2.18849887439791, 'UPHENO:0076772', 'abnormal cranial nerve morphology'),
(137108, 'HP:0011348', 'Abnormal sixth cranial nerve morphology', 'XPO:0100247', 'abnormal cranial ganglion', 0.4222222222222222, 6.642668884102504, 1.674718608522688, 'HP:0410008', 'Abnormality of the peripheral nervous system'),
(137109, 'HP:0011348', 'Abnormal sixth cranial nerve morphology', 'XPO:0127813', 'abnormally localised peripheral nerve', 0.4074074074074074, 8.429051634704384, 1.853121170727398, 'HP:0045010', 'Abnormal peripheral nerve morphology by anatomical site'),
(137110, 'HP:0011348', 'Abnormal sixth cranial nerve morphology', 'XPO:0131563', 'abnormally localised frontal nerve', 0.40625, 8.429051634704384, 1.8504870241638163, 'HP:0045010', 'Abnormal peripheral nerve morphology by anatomical site'),
(137111, 'HP:0011348', 'Abnormal sixth cranial nerve morphology', 'XPO:0101335', 'abnormal vagus nerve', 0.5, 8.429051634704384, 2.0529310308318185, 'HP:0045010', 'Abnormal peripheral nerve morphology by anatomical site'),
(137112, 'HP:0011348', 'Abnormal sixth cranial nerve morphology', 'XPO:0101204', 'abnormal peripheral nerve', 0.5116279069767442, 8.429051634704384, 2.076665126028438, 'HP:0045010', 'Abnormal peripheral nerve morphology by anatomical site'),
(137113, 'HP:0011348', 'Abnormal sixth cranial nerve morphology', 'XPO:0127841', 'abnormally localised ampullary nerve', 0.44776119402985076, 9.57905464648184, 2.0710212326738464, 'UPHENO:0076772', 'abnormal cranial nerve morphology'),
(137114, 'HP:0011348', 'Abnormal sixth cranial nerve morphology', 'XPO:0103053', 'abnormal oculomotor nerve morphology', 0.44776119402985076, 9.57905464648184, 2.0710212326738464, 'UPHENO:0076772', 'abnormal cranial nerve morphology'),
(137115, 'HP:0011348', 'Abnormal sixth cranial nerve morphology', 'XPO:0102839', 'abnormal glossopharyngeal nerve morphology', 0.4166666666666667, 9.57905464648184, 1.9978170009706677, 'UPHENO:0076772', 'abnormal cranial nerve morphology'),
(137116, 'HP:0011348', 'Abnormal sixth cranial nerve morphology', 'XPO:0101030', 'abnormal spinal nerve', 0.4888888888888889, 8.429051634704384, 2.0299925339955562, 'HP:0045010', 'Abnormal peripheral nerve morphology by anatomical site'),
(137117, 'HP:0011348', 'Abnormal sixth cranial nerve morphology', 'XPO:0101234', 'abnormal gasserian ganglion', 0.41304347826086957, 6.642668884102504, 1.6564151233386355, 'HP:0410008', 'Abnormality of the peripheral nervous system'),
(137118, 'HP:0011348', 'Abnormal sixth cranial nerve morphology', 'XPO:0100832', 'abnormal sciatic nerve', 0.41509433962264153, 8.429051634704384, 1.8705217512642733, 'HP:0045010', 'Abnormal peripheral nerve morphology by anatomical site'),
(137119, 'HP:0011348', 'Abnormal sixth cranial nerve morphology', 'XPO:0131688', 'abnormal mandibular nerve', 0.5098039215686274, 8.429051634704384, 2.0729601005510805, 'HP:0045010', 'Abnormal peripheral nerve morphology by anatomical site'),
(137120, 'HP:0011348', 'Abnormal sixth cranial nerve morphology', 'XPO:0102866', 'abnormal gasserian ganglion morphology', 0.40625, 7.318748312764234, 1.7243089926287778, 'HP:0000759', 'Abnormal peripheral nervous system morphology'),
(137121, 'HP:0011348', 'Abnormal sixth cranial nerve morphology', 'XPO:0103173', 'abnormal olfactory nerve morphology', 0.42857142857142855, 9.57905464648184, 2.0261562462471896, 'UPHENO:0076772', 'abnormal cranial nerve morphology'),
(137122, 'HP:0011348', 'Abnormal sixth cranial nerve morphology', 'XPO:0101934', 'abnormal epibranchial placode morphology', 0.41935483870967744, 7.318748312764234, 1.7518996884114024, 'HP:0000759', 'Abnormal peripheral nervous system morphology'),
(137123, 'HP:0011348', 'Abnormal sixth cranial nerve morphology', 'XPO:0101743', 'abnormal cranial nerve morphology', 0.46875, 9.57905464648184, 2.119004923434196, 'UPHENO:0076772', 'abnormal cranial nerve morphology'),
(137124, 'HP:0011348', 'Abnormal sixth cranial nerve morphology', 'XPO:0100167', 'abnormal nerve', 0.5116279069767442, 8.429051634704384, 2.076665126028438, 'HP:0045010', 'Abnormal peripheral nerve morphology by anatomical site'),
(137125, 'HP:0011348', 'Abnormal sixth cranial nerve morphology', 'XPO:0101427', 'abnormal ampullary nerve', 0.5454545454545454, 9.57905464648184, 2.285812524701228, 'UPHENO:0076772', 'abnormal cranial nerve morphology'),
(137126, 'HP:0011348', 'Abnormal sixth cranial nerve morphology', 'XPO:0100111', 'abnormal cranial nerve', 0.5306122448979592, 8.429051634704384, 2.114842313330076, 'HP:0045010', 'Abnormal peripheral nerve morphology by anatomical site'),
(137127, 'HP:0011348', 'Abnormal sixth cranial nerve morphology', 'XPO:0100110', 'abnormal trigeminal nerve', 0.52, 8.429051634704384, 2.093587077254319, 'HP:0045010', 'Abnormal peripheral nerve morphology by anatomical site'),
(137128, 'HP:0011348', 'Abnormal sixth cranial nerve morphology', 'XPO:0131572', 'abnormally localised mandibular nerve', 0.40625, 8.429051634704384, 1.8504870241638163, 'HP:0045010', 'Abnormal peripheral nerve morphology by anatomical site'),
(137129, 'HP:0011348', 'Abnormal sixth cranial nerve morphology', 'XPO:0141300', 'abnormal mandibular nerve morphology', 0.44776119402985076, 9.57905464648184, 2.0710212326738464, 'UPHENO:0076772', 'abnormal cranial nerve morphology'),
(137130, 'HP:0011348', 'Abnormal sixth cranial nerve morphology', 'XPO:0127421', 'abnormally localised oculomotor nerve', 0.40625, 8.429051634704384, 1.8504870241638163, 'HP:0045010', 'Abnormal peripheral nerve morphology by anatomical site'),
(137131, 'HP:0011348', 'Abnormal sixth cranial nerve morphology', 'XPO:0125655', 'absent accessory nerve', 0.42857142857142855, 9.57905464648184, 2.0261562462471896, 'UPHENO:0076772', 'abnormal cranial nerve morphology'),
(137132, 'HP:0011348', 'Abnormal sixth cranial nerve morphology', 'XPO:0101541', 'abnormal olfactory nerve', 0.5, 8.429051634704384, 2.0529310308318185, 'HP:0045010', 'Abnormal peripheral nerve morphology by anatomical site'),
(137133, 'HP:0011348', 'Abnormal sixth cranial nerve morphology', 'XPO:0102967', 'abnormal vagus nerve morphology', 0.42857142857142855, 9.57905464648184, 2.0261562462471896, 'UPHENO:0076772', 'abnormal cranial nerve morphology'),
(137134, 'HP:0011348', 'Abnormal sixth cranial nerve morphology', 'XPO:0131498', 'absent cephalic nerve', 0.40625, 8.429051634704384, 1.8504870241638163, 'HP:0045010', 'Abnormal peripheral nerve morphology by anatomical site'),
(137135, 'HP:0011348', 'Abnormal sixth cranial nerve morphology', 'XPO:0101207', 'abnormal glossopharyngeal nerve', 0.5, 8.429051634704384, 2.0529310308318185, 'HP:0045010', 'Abnormal peripheral nerve morphology by anatomical site'),
(137136, 'HP:0011348', 'Abnormal sixth cranial nerve morphology', 'XPO:0102480', 'abnormal glossopharyngeal epibranchial placode morphology', 0.40625, 7.318748312764234, 1.7243089926287778, 'HP:0000759', 'Abnormal peripheral nervous system morphology'),
(137137, 'HP:0011348', 'Abnormal sixth cranial nerve morphology', 'XPO:0101878', 'abnormal lateral line ganglion morphology', 0.4126984126984127, 7.318748312764234, 1.7379401058773531, 'HP:0000759', 'Abnormal peripheral nervous system morphology'),
(137138, 'HP:0011348', 'Abnormal sixth cranial nerve morphology', 'XPO:0103059', 'abnormal ampullary nerve morphology', 0.42857142857142855, 9.57905464648184, 2.0261562462471896, 'UPHENO:0076772', 'abnormal cranial nerve morphology'),
(137139, 'HP:0011348', 'Abnormal sixth cranial nerve morphology', 'XPO:0126866', 'abnormally localised vestibulocochlear nerve', 0.4411764705882353, 9.57905464648184, 2.0557367342407185, 'UPHENO:0076772', 'abnormal cranial nerve morphology'),
(137140, 'HP:0011348', 'Abnormal sixth cranial nerve morphology', 'XPO:0102481', 'abnormal abducens nerve morphology', 0.45588235294117646, 13.7526182249875, 2.5039121301493403, 'HP:0011348', 'Abnormal sixth cranial nerve morphology'),
(137141, 'HP:0011348', 'Abnormal sixth cranial nerve morphology', 'XPO:0141303', 'abnormal nasociliary nerve morphology', 0.44776119402985076, 9.57905464648184, 2.0710212326738464, 'UPHENO:0076772', 'abnormal cranial nerve morphology'),
(137142, 'HP:0011348', 'Abnormal sixth cranial nerve morphology', 'XPO:0101185', 'abnormal vestibulocochlear nerve', 0.5555555555555556, 9.57905464648184, 2.3068803666040516, 'UPHENO:0076772', 'abnormal cranial nerve morphology'),
(137143, 'HP:0011348', 'Abnormal sixth cranial nerve morphology', 'XPO:0102259', 'abnormal pharyngeal region morphology', 0.4090909090909091, 4.5318002188002176, 1.3615866741883758, 'UPHENO:0087907', 'abnormal head morphology'),
(137144, 'HP:0011348', 'Abnormal sixth cranial nerve morphology', 'XPO:0128377', 'decreased size of the cranial nerve', 0.40540540540540543, 9.57905464648184, 1.9706345506860228, 'UPHENO:0076772', 'abnormal cranial nerve morphology'),
(137145, 'HP:0011348', 'Abnormal sixth cranial nerve morphology', 'XPO:0100849', 'abnormal abducens nerve', 0.6078431372549019, 13.7526182249875, 2.8912686847377818, 'HP:0011348', 'Abnormal sixth cranial nerve morphology'),
(137146, 'HP:0011348', 'Abnormal sixth cranial nerve morphology', 'XPO:0101933', 'abnormal vagal epibranchial placode morphology', 0.40625, 7.318748312764234, 1.7243089926287778, 'HP:0000759', 'Abnormal peripheral nervous system morphology'),
(137147, 'HP:0011348', 'Abnormal sixth cranial nerve morphology', 'XPO:0102643', 'abnormal facial epibranchial placode morphology', 0.40625, 7.318748312764234, 1.7243089926287778, 'HP:0000759', 'Abnormal peripheral nervous system morphology'),
(137148, 'HP:0011348', 'Abnormal sixth cranial nerve morphology', 'XPO:0127043', 'abnormally localised abducens nerve', 0.47692307692307695, 13.7526182249875, 2.5610429515354527, 'HP:0011348', 'Abnormal sixth cranial nerve morphology'),
(137149, 'HP:0011348', 'Abnormal sixth cranial nerve morphology', 'XPO:0102371', 'abnormal hypoglossal nerve morphology', 0.410958904109589, 9.57905464648184, 1.9840861372238967, 'UPHENO:0076772', 'abnormal cranial nerve morphology'),
(137150, 'HP:0011348', 'Abnormal sixth cranial nerve morphology', 'XPO:0140188', 'abnormally necrotic abducens nerve', 0.4025974025974026, 13.7526182249875, 2.3530338663720225, 'HP:0011348', 'Abnormal sixth cranial nerve morphology'),
(137151, 'HP:0011348', 'Abnormal sixth cranial nerve morphology', 'XPO:0131536', 'abnormally localised cephalic nerve', 0.43333333333333335, 8.429051634704384, 1.911174780522502, 'HP:0045010', 'Abnormal peripheral nerve morphology by anatomical site'),
(137152, 'HP:0011348', 'Abnormal sixth cranial nerve morphology', 'XPO:0127971', 'abnormally localised trochlear nerve', 0.40625, 8.429051634704384, 1.8504870241638163, 'HP:0045010', 'Abnormal peripheral nerve morphology by anatomical site'),
(137153, 'HP:0011348', 'Abnormal sixth cranial nerve morphology', 'XPO:0126817', 'abnormally localised trigeminal nerve', 0.40625, 8.429051634704384, 1.8504870241638163, 'HP:0045010', 'Abnormal peripheral nerve morphology by anatomical site'),
(137154, 'HP:0011348', 'Abnormal sixth cranial nerve morphology', 'XPO:0126179', 'absent ampullary nerve', 0.410958904109589, 9.57905464648184, 1.9840861372238967, 'UPHENO:0076772', 'abnormal cranial nerve morphology'),
(137155, 'HP:0005401', 'Recurrent candida infections', 'XPO:0100599', 'abnormal adult immune system', 0.43333333333333335, 5.64885357140806, 1.5645563421015427, 'HP:0002715', 'Abnormality of the immune system'),
(137156, 'HP:0005401', 'Recurrent candida infections', 'XPO:0101221', 'abnormal larval immune system', 0.43333333333333335, 5.64885357140806, 1.5645563421015427, 'HP:0002715', 'Abnormality of the immune system'),
(137157, 'HP:0005401', 'Recurrent candida infections', 'XPO:0100745', 'abnormal anterior lymph sac', 0.40625, 5.64885357140806, 1.5148751642906173, 'HP:0002715', 'Abnormality of the immune system'),
(137158, 'HP:0005401', 'Recurrent candida infections', 'XPO:0100581', 'abnormal immune system', 0.4482758620689655, 5.64885357140806, 1.5913028324062968, 'HP:0002715', 'Abnormality of the immune system'),
(137159, 'HP:0005401', 'Recurrent candida infections', 'XPO:0100232', 'abnormal lymphatic system', 0.4482758620689655, 5.64885357140806, 1.5913028324062968, 'HP:0002715', 'Abnormality of the immune system'),
(137160, 'HP:0005401', 'Recurrent candida infections', 'XPO:0101451', 'abnormal dorsal lymph space', 0.41935483870967744, 5.64885357140806, 1.5391147060347428, 'HP:0002715', 'Abnormality of the immune system'),
(137161, 'HP:0003635', 'Loss of subcutaneous adipose tissue in limbs', 'XPO:0115491', 'abnormally increased distribution of connective tissue', 0.4090909090909091, 6.985637650836012, 1.6904913064432443, 'UPHENO:0002712', 'abnormal connective tissue'),
(137162, 'HP:0003635', 'Loss of subcutaneous adipose tissue in limbs', 'XPO:0131319', 'abnormally decreased number of stromal cell', 0.4166666666666667, 6.985637650836012, 1.70607220085054, 'UPHENO:0002712', 'abnormal connective tissue'),
(137163, 'HP:0003635', 'Loss of subcutaneous adipose tissue in limbs', 'XPO:0102009', 'abnormal connective tissue morphology', 0.4186046511627907, 6.985637650836012, 1.710035207818209, 'UPHENO:0002712', 'abnormal connective tissue'),
(137164, 'HP:0003635', 'Loss of subcutaneous adipose tissue in limbs', 'XPO:0102320', 'abnormal adipose tissue morphology', 0.4444444444444444, 10.114017760664272, 2.1201695698079615, 'UPHENO:0076797', 'abnormal adipose tissue morphology'),
(137165, 'HP:0003635', 'Loss of subcutaneous adipose tissue in limbs', 'XPO:0142065', 'abnormally decreased number of desmosome', 0.40476190476190477, 6.742408026385282, 1.6519896838181714, 'UPHENO:0035147', 'abnormally decreased number of anatomical entity in the multicellular organism'),
(137166, 'HP:0033129', 'Abnormal shoulder physiology', 'XPO:0102217', 'abnormal elastica externa morphology', 0.40540540540540543, 4.3395673355180735, 1.3263800567483512, 'UPHENO:0002964', 'abnormal skeletal system'),
(137167, 'HP:0033129', 'Abnormal shoulder physiology', 'XPO:0100882', 'abnormal perichondrial cell', 0.4117647058823529, 4.3395673355180735, 1.3367425584480601, 'UPHENO:0002964', 'abnormal skeletal system'),
(137168, 'HP:0033129', 'Abnormal shoulder physiology', 'XPO:0101348', 'abnormal perichordal tissue', 0.4375, 4.3395673355180735, 1.3778826906849353, 'UPHENO:0002964', 'abnormal skeletal system'),
(137169, 'HP:0033129', 'Abnormal shoulder physiology', 'XPO:0125099', 'absent elastica externa', 0.40540540540540543, 4.3395673355180735, 1.3263800567483512, 'UPHENO:0002964', 'abnormal skeletal system'),
(137170, 'HP:0033129', 'Abnormal shoulder physiology', 'XPO:0100325', 'abnormal axial skeleton', 0.4375, 4.3395673355180735, 1.3778826906849353, 'UPHENO:0002964', 'abnormal skeletal system'),
(137171, 'HP:0033129', 'Abnormal shoulder physiology', 'XPO:0100829', 'abnormal postcranial axial skeleton', 0.42424242424242425, 4.3395673355180735, 1.3568450783281876, 'UPHENO:0002964', 'abnormal skeletal system'),
(137172, 'HP:0033129', 'Abnormal shoulder physiology', 'XPO:0100123', 'abnormal pelvic girdle', 0.42424242424242425, 4.3395673355180735, 1.3568450783281876, 'UPHENO:0002964', 'abnormal skeletal system'),
(137173, 'HP:0033129', 'Abnormal shoulder physiology', 'XPO:0126722', 'abnormally localised elastica externa', 0.4166666666666667, 4.3395673355180735, 1.3446758183539496, 'UPHENO:0002964', 'abnormal skeletal system'),
(137174, 'HP:0033129', 'Abnormal shoulder physiology', 'XPO:0100640', 'abnormal notochordal sheath', 0.4827586206896552, 4.3395673355180735, 1.4473988881039626, 'UPHENO:0002964', 'abnormal skeletal system'),
(137175, 'HP:0033129', 'Abnormal shoulder physiology', 'XPO:0100512', 'abnormal cranial skeleton', 0.42424242424242425, 4.3395673355180735, 1.3568450783281876, 'UPHENO:0002964', 'abnormal skeletal system'),
(137176, 'HP:0033129', 'Abnormal shoulder physiology', 'XPO:0101174', 'abnormal articular system', 0.4827586206896552, 4.3395673355180735, 1.4473988881039626, 'UPHENO:0002964', 'abnormal skeletal system'),
(137177, 'HP:0033129', 'Abnormal shoulder physiology', 'XPO:0100585', 'abnormal elastica externa', 0.5185185185185185, 4.3395673355180735, 1.5000486744849937, 'UPHENO:0002964', 'abnormal skeletal system'),
(137178, 'HP:0033129', 'Abnormal shoulder physiology', 'XPO:0100377', 'abnormal connective tissue', 0.41379310344827586, 3.9037819259951223, 1.270967363209146, 'HP:0033127', 'Abnormality of the musculoskeletal system'),
(137179, 'HP:0033129', 'Abnormal shoulder physiology', 'XPO:0101586', 'abnormal joint', 0.42424242424242425, 4.3395673355180735, 1.3568450783281876, 'UPHENO:0002964', 'abnormal skeletal system'),
(137180, 'HP:0033129', 'Abnormal shoulder physiology', 'XPO:0102097', 'abnormal skeletal system morphology', 0.40540540540540543, 4.3395673355180735, 1.3263800567483512, 'UPHENO:0002964', 'abnormal skeletal system'),
(137181, 'HP:0033129', 'Abnormal shoulder physiology', 'XPO:0125380', 'absent skeletal system', 0.40540540540540543, 4.3395673355180735, 1.3263800567483512, 'UPHENO:0002964', 'abnormal skeletal system'),
(137182, 'HP:0033129', 'Abnormal shoulder physiology', 'XPO:0100973', 'abnormal dermal skeleton', 0.4375, 4.3395673355180735, 1.3778826906849353, 'UPHENO:0002964', 'abnormal skeletal system'),
(137183, 'HP:0033129', 'Abnormal shoulder physiology', 'XPO:0141718', 'abnormal posterior notochord', 0.4827586206896552, 4.3395673355180735, 1.4473988881039626, 'UPHENO:0002964', 'abnormal skeletal system'),
(137184, 'HP:0033129', 'Abnormal shoulder physiology', 'XPO:0107285', 'abnormal flexural organ', 0.4827586206896552, 4.3395673355180735, 1.4473988881039626, 'UPHENO:0002964', 'abnormal skeletal system'),
(137185, 'HP:0033129', 'Abnormal shoulder physiology', 'XPO:0100498', 'abnormal endoskeleton', 0.4375, 4.3395673355180735, 1.3778826906849353, 'UPHENO:0002964', 'abnormal skeletal system'),
(137186, 'HP:0033129', 'Abnormal shoulder physiology', 'XPO:0100910', 'abnormal vacuolated notochordal tissue', 0.4375, 4.3395673355180735, 1.3778826906849353, 'UPHENO:0002964', 'abnormal skeletal system'),
(137187, 'HP:0033129', 'Abnormal shoulder physiology', 'XPO:0100350', 'abnormal appendicular skeleton', 0.4375, 4.3395673355180735, 1.3778826906849353, 'UPHENO:0002964', 'abnormal skeletal system'),
(137188, 'HP:0033129', 'Abnormal shoulder physiology', 'XPO:0127584', 'abnormally localised articular system', 0.40540540540540543, 4.3395673355180735, 1.3263800567483512, 'UPHENO:0002964', 'abnormal skeletal system'),
(137189, 'HP:0033129', 'Abnormal shoulder physiology', 'XPO:0100228', 'abnormal skeletal subdivision', 0.45161290322580644, 4.3395673355180735, 1.399930213666808, 'UPHENO:0002964', 'abnormal skeletal system'),
(137190, 'HP:0033129', 'Abnormal shoulder physiology', 'XPO:0100004', 'abnormal cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(137191, 'HP:0033129', 'Abnormal shoulder physiology', 'XPO:0127013', 'abnormally localised skeletal system', 0.4166666666666667, 4.3395673355180735, 1.3446758183539496, 'UPHENO:0002964', 'abnormal skeletal system'),
(137192, 'HP:0033129', 'Abnormal shoulder physiology', 'XPO:0101484', 'abnormal bone marrow', 0.4117647058823529, 4.3395673355180735, 1.3367425584480601, 'UPHENO:0002964', 'abnormal skeletal system'),
(137193, 'HP:0033129', 'Abnormal shoulder physiology', 'XPO:0100378', 'abnormal perichondrium', 0.4666666666666667, 4.3395673355180735, 1.4230711237467255, 'UPHENO:0002964', 'abnormal skeletal system'),
(137194, 'HP:0033129', 'Abnormal shoulder physiology', 'XPO:0100465', 'abnormal skeletal system', 0.5, 4.3395673355180735, 1.473018556488355, 'UPHENO:0002964', 'abnormal skeletal system'),
(137195, 'HP:0033129', 'Abnormal shoulder physiology', 'XPO:0141714', 'abnormal anterior notochord', 0.4827586206896552, 4.3395673355180735, 1.4473988881039626, 'UPHENO:0002964', 'abnormal skeletal system'),
(137196, 'HP:0033129', 'Abnormal shoulder physiology', 'XPO:0100461', 'abnormal craniofacial skeleton', 0.4117647058823529, 4.3395673355180735, 1.3367425584480601, 'UPHENO:0002964', 'abnormal skeletal system'),
(137197, 'HP:0033129', 'Abnormal shoulder physiology', 'XPO:0100422', 'abnormal notochord', 0.5, 4.3395673355180735, 1.473018556488355, 'UPHENO:0002964', 'abnormal skeletal system'),
(137198, 'HP:0033129', 'Abnormal shoulder physiology', 'XPO:0100935', 'abnormal skeleton', 0.4666666666666667, 4.3395673355180735, 1.4230711237467255, 'UPHENO:0002964', 'abnormal skeletal system'),
(137199, 'HP:0002435', 'Meningocele', 'XPO:0101664', 'abnormal nervous system morphology', 0.40425531914893614, 4.7814666189787065, 1.3902997209433732, 'HP:0012639', 'Abnormal nervous system morphology'),
(137200, 'HP:0002435', 'Meningocele', 'XPO:0101802', 'abnormal anterior neural tube morphology', 0.4444444444444444, 9.151353911937244, 2.0167469859418268, 'UPHENO:0087363', 'abnormal neural tube morphology'),
(137201, 'HP:0002435', 'Meningocele', 'XPO:0101768', 'abnormal neural tube morphology', 0.4642857142857143, 11.582693223545188, 2.3189823191749395, 'UPHENO:0020641', 'abnormal neural tube morphology'),
(137202, 'HP:0002435', 'Meningocele', 'XPO:0102903', 'abnormal roof plate morphology', 0.4067796610169492, 9.151353911937244, 1.9294000731170204, 'UPHENO:0087363', 'abnormal neural tube morphology'),
(137203, 'HP:0002435', 'Meningocele', 'XPO:0102419', 'abnormal posterior neural tube morphology', 0.4444444444444444, 9.151353911937244, 2.0167469859418268, 'UPHENO:0087363', 'abnormal neural tube morphology'),
(137204, 'HP:0002435', 'Meningocele', 'XPO:0102444', 'abnormal sulcus limitans of neural tube morphology', 0.41379310344827586, 9.151353911937244, 1.9459617509021168, 'UPHENO:0087363', 'abnormal neural tube morphology'),
(137205, 'HP:0002435', 'Meningocele', 'XPO:0103025', 'abnormal dorsolateral neural tube morphology', 0.4444444444444444, 9.151353911937244, 2.0167469859418268, 'UPHENO:0087363', 'abnormal neural tube morphology'),
(137206, 'HP:0002435', 'Meningocele', 'XPO:0103470', 'abnormal closing of the posterior neural tube', 0.42857142857142855, 9.151353911937244, 1.9804062258540989, 'UPHENO:0087363', 'abnormal neural tube morphology'),
(137207, 'HP:0002435', 'Meningocele', 'XPO:0102490', 'abnormal presumptive midbrain-hindbrain boundary morphology', 0.45098039215686275, 6.472691136191403, 1.7085247399174086, 'UPHENO:0088123', 'abnormal embryonic tissue morphology'),
(137208, 'HP:0002435', 'Meningocele', 'XPO:0140125', 'abnormally necrotic presumptive midbrain-hindbrain boundary', 0.41818181818181815, 6.472691136191403, 1.6452239202801118, 'UPHENO:0088123', 'abnormal embryonic tissue morphology'),
(137209, 'HP:0002435', 'Meningocele', 'XPO:0131750', 'abnormal opening of the anterior neural tube', 0.42857142857142855, 9.151353911937244, 1.9804062258540989, 'UPHENO:0087363', 'abnormal neural tube morphology'),
(137210, 'HP:0002435', 'Meningocele', 'XPO:0142058', 'abnormal cerebrospinal fluid morphology', 0.4375, 5.483278994082134, 1.5488494310006167, 'HP:0002011', 'Morphological central nervous system abnormality'),
(137211, 'HP:0002435', 'Meningocele', 'XPO:0140397', 'abnormally necrotic ventrolateral neural tube', 0.41379310344827586, 9.151353911937244, 1.9459617509021168, 'UPHENO:0087363', 'abnormal neural tube morphology'),
(137212, 'HP:0002435', 'Meningocele', 'XPO:0101790', 'abnormal neuromere morphology', 0.4117647058823529, 5.483278994082134, 1.502604659339613, 'HP:0002011', 'Morphological central nervous system abnormality'),
(137213, 'HP:0002435', 'Meningocele', 'XPO:0128950', 'decreased size of the presumptive midbrain-hindbrain boundary', 0.40350877192982454, 6.472691136191403, 1.6161026116697088, 'UPHENO:0088123', 'abnormal embryonic tissue morphology'),
(137214, 'HP:0002435', 'Meningocele', 'XPO:0131746', 'abnormal neural tube closure', 0.7804878048780488, 12.484129389061598, 3.1214917495777916, 'UPHENO:0051077', 'abnormal neural tube closure'),
(137215, 'HP:0002435', 'Meningocele', 'XPO:0101796', 'abnormal neural nucleus morphology', 0.42, 5.483278994082134, 1.5175563177406288, 'HP:0002011', 'Morphological central nervous system abnormality'),
(137216, 'HP:0002435', 'Meningocele', 'XPO:0115628', 'abnormally open neural tube', 0.4482758620689655, 11.582693223545188, 2.2786491151261274, 'UPHENO:0020641', 'abnormal neural tube morphology'),
(137217, 'HP:0002435', 'Meningocele', 'XPO:0103133', 'abnormal parabrachial area morphology', 0.40384615384615385, 5.483278994082134, 1.4880863994491305, 'HP:0002011', 'Morphological central nervous system abnormality'),
(137218, 'HP:0002435', 'Meningocele', 'XPO:0102667', 'abnormal ventrolateral neural tube morphology', 0.4444444444444444, 9.151353911937244, 2.0167469859418268, 'UPHENO:0087363', 'abnormal neural tube morphology'),
(137219, 'HP:0002435', 'Meningocele', 'XPO:0130428', 'increased size of the presumptive midbrain-hindbrain boundary', 0.40350877192982454, 6.472691136191403, 1.6161026116697088, 'UPHENO:0088123', 'abnormal embryonic tissue morphology'),
(137220, 'HP:0002435', 'Meningocele', 'XPO:0139814', 'abnormally necrotic neural tube', 0.40625, 11.582693223545188, 2.1692093310847693, 'UPHENO:0020641', 'abnormal neural tube morphology'),
(137221, 'HP:0002435', 'Meningocele', 'XPO:0103002', 'abnormal floor plate morphology', 0.42105263157894735, 9.151353911937244, 1.9629573727239904, 'UPHENO:0087363', 'abnormal neural tube morphology'),
(137222, 'HP:0002435', 'Meningocele', 'XPO:0140414', 'abnormally necrotic posterior neural tube', 0.41379310344827586, 9.151353911937244, 1.9459617509021168, 'UPHENO:0087363', 'abnormal neural tube morphology'),
(137223, 'HP:0002435', 'Meningocele', 'XPO:0142031', 'abnormally necrotic cerebrospinal fluid', 0.4117647058823529, 5.483278994082134, 1.502604659339613, 'HP:0002011', 'Morphological central nervous system abnormality'),
(137224, 'HP:0002435', 'Meningocele', 'XPO:0101663', 'abnormal central nervous system morphology', 0.42857142857142855, 5.483278994082134, 1.5329633758669794, 'HP:0002011', 'Morphological central nervous system abnormality'),
(137225, 'HP:0002435', 'Meningocele', 'XPO:0140183', 'abnormally necrotic dorsolateral neural tube', 0.41379310344827586, 9.151353911937244, 1.9459617509021168, 'UPHENO:0087363', 'abnormal neural tube morphology'),
(137226, 'HP:0002435', 'Meningocele', 'XPO:0139865', 'abnormally necrotic anterior neural tube', 0.41379310344827586, 9.151353911937244, 1.9459617509021168, 'UPHENO:0087363', 'abnormal neural tube morphology'),
(137227, 'HP:0002435', 'Meningocele', 'XPO:0103453', 'abnormal incomplete closing of the neural tube', 0.43333333333333335, 11.582693223545188, 2.240349763661078, 'UPHENO:0020641', 'abnormal neural tube morphology'),
(137228, 'HP:0034322', 'Reduced galactocerebrosidase activity', 'XPO:0100377', 'abnormal connective tissue', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(137229, 'HP:0034322', 'Reduced galactocerebrosidase activity', 'XPO:0100084', 'abnormal anatomical group', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(137230, 'HP:0034322', 'Reduced galactocerebrosidase activity', 'XPO:0101220', 'abnormal centriole', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(137231, 'HP:0034322', 'Reduced galactocerebrosidase activity', 'XPO:0131685', 'abnormal cortical actin cytoskeleton', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(137232, 'HP:0034322', 'Reduced galactocerebrosidase activity', 'XPO:0107262', 'abnormal left-right axis', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(137233, 'HP:0034322', 'Reduced galactocerebrosidase activity', 'XPO:0100289', 'abnormal chondroblast', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(137234, 'HP:0034322', 'Reduced galactocerebrosidase activity', 'XPO:0131666', 'abnormal adherens junction', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(137235, 'HP:0034322', 'Reduced galactocerebrosidase activity', 'XPO:0101109', 'abnormal egg cell-free extract', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(137236, 'HP:0034322', 'Reduced galactocerebrosidase activity', 'XPO:0101221', 'abnormal larval immune system', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(137237, 'HP:0034322', 'Reduced galactocerebrosidase activity', 'XPO:0141748', 'abnormal gas homeostasis', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(137238, 'HP:0034322', 'Reduced galactocerebrosidase activity', 'XPO:0141850', 'abnormal galactose metabolic process', 0.4230769230769231, 4.758907843651163, 1.418937661667548, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(137239, 'HP:0034322', 'Reduced galactocerebrosidase activity', 'XPO:0100574', 'abnormal gastrula cell', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(137240, 'HP:0034322', 'Reduced galactocerebrosidase activity', 'XPO:0141767', 'abnormal temperature homeostasis', 0.44, 4.758907843651163, 1.447038165082909, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(137241, 'HP:0034322', 'Reduced galactocerebrosidase activity', 'XPO:0101472', 'abnormal zygote cortex', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(137242, 'HP:0034322', 'Reduced galactocerebrosidase activity', 'XPO:0141778', 'abnormal biosynthetic process', 0.5238095238095238, 4.758907843651163, 1.5788480773767701, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(137243, 'HP:0034322', 'Reduced galactocerebrosidase activity', 'XPO:0100638', 'abnormal polar body', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(137244, 'HP:0034322', 'Reduced galactocerebrosidase activity', 'XPO:0141782', 'abnormal methylation', 0.5238095238095238, 4.758907843651163, 1.5788480773767701, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(137245, 'HP:0034322', 'Reduced galactocerebrosidase activity', 'XPO:0141792', 'abnormal small molecule metabolic process', 0.5238095238095238, 4.758907843651163, 1.5788480773767701, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(137246, 'HP:0034322', 'Reduced galactocerebrosidase activity', 'XPO:0100108', 'abnormal cell part', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(137247, 'HP:0034322', 'Reduced galactocerebrosidase activity', 'XPO:0100062', 'abnormal anatomical space', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(137248, 'HP:0034322', 'Reduced galactocerebrosidase activity', 'XPO:0141499', 'abnormal tadpole', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(137249, 'HP:0034322', 'Reduced galactocerebrosidase activity', 'XPO:0100032', 'abnormal nervous system', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(137250, 'HP:0034322', 'Reduced galactocerebrosidase activity', 'XPO:0141860', 'abnormal malate-aspartate shuttle', 0.5, 4.758907843651163, 1.5425478669479211, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(137251, 'HP:0034322', 'Reduced galactocerebrosidase activity', 'XPO:0141864', 'abnormal 5-methylcytosine metabolic process', 0.4230769230769231, 4.758907843651163, 1.418937661667548, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(137252, 'HP:0034322', 'Reduced galactocerebrosidase activity', 'XPO:0100307', 'abnormal blastomere', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(137253, 'HP:0034322', 'Reduced galactocerebrosidase activity', 'XPO:0142057', 'abnormal desmosome', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(137254, 'HP:0034322', 'Reduced galactocerebrosidase activity', 'XPO:0101297', 'abnormal barrier cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(137255, 'HP:0034322', 'Reduced galactocerebrosidase activity', 'XPO:0141264', 'abnormal schooling behavior', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(137256, 'HP:0034322', 'Reduced galactocerebrosidase activity', 'XPO:0101461', 'abnormal sperm entry point', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(137257, 'HP:0034322', 'Reduced galactocerebrosidase activity', 'XPO:0141772', 'abnormal water homeostasis', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(137258, 'HP:0034322', 'Reduced galactocerebrosidase activity', 'XPO:0100802', 'abnormal exocrine cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(137259, 'HP:0034322', 'Reduced galactocerebrosidase activity', 'XPO:0100917', 'abnormal stage III oocyte', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(137260, 'HP:0034322', 'Reduced galactocerebrosidase activity', 'XPO:0100546', 'abnormal whole organism', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(137261, 'HP:0034322', 'Reduced galactocerebrosidase activity', 'XPO:0141880', 'abnormal ethanolamine metabolic process', 0.44, 4.758907843651163, 1.447038165082909, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(137262, 'HP:0034322', 'Reduced galactocerebrosidase activity', 'XPO:0100429', 'abnormal spermatid', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(137263, 'HP:0034322', 'Reduced galactocerebrosidase activity', 'XPO:0100423', 'abnormal process', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(137264, 'HP:0034322', 'Reduced galactocerebrosidase activity', 'XPO:0141781', 'abnormal secondary metabolic process', 0.5238095238095238, 4.758907843651163, 1.5788480773767701, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(137265, 'HP:0034322', 'Reduced galactocerebrosidase activity', 'XPO:0141790', 'abnormal cellular metabolic process', 0.5, 4.758907843651163, 1.5425478669479211, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(137266, 'HP:0034322', 'Reduced galactocerebrosidase activity', 'XPO:0141743', 'abnormal chemical homeostasis within a tissue', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(137267, 'HP:0034322', 'Reduced galactocerebrosidase activity', 'XPO:0141900', 'abnormal mannose metabolic process', 0.4230769230769231, 4.758907843651163, 1.418937661667548, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(137268, 'HP:0034322', 'Reduced galactocerebrosidase activity', 'XPO:0141866', 'abnormal dicarboxylic acid metabolic process', 0.4074074074074074, 4.758907843651163, 1.392413123563799, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(137269, 'HP:0034322', 'Reduced galactocerebrosidase activity', 'XPO:0131691', 'abnormal molecular function', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(137270, 'HP:0034322', 'Reduced galactocerebrosidase activity', 'XPO:0107260', 'abnormal anterior-posterior axis', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(137271, 'HP:0034322', 'Reduced galactocerebrosidase activity', 'XPO:0101264', 'abnormal mitotic spindle', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(137272, 'HP:0034322', 'Reduced galactocerebrosidase activity', 'XPO:0101498', 'abnormal stage II oocyte', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(137273, 'HP:0034322', 'Reduced galactocerebrosidase activity', 'XPO:0100533', 'abnormal melanoblast', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(137274, 'HP:0034322', 'Reduced galactocerebrosidase activity', 'XPO:0100888', 'abnormal microtubule', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(137275, 'HP:0034322', 'Reduced galactocerebrosidase activity', 'XPO:0131723', 'abnormal pathway-restricted SMAD protein phosphorylation', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(137276, 'HP:0034322', 'Reduced galactocerebrosidase activity', 'XPO:0100081', 'abnormal anatomical entity in vitro', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(137277, 'HP:0034322', 'Reduced galactocerebrosidase activity', 'XPO:0101366', 'abnormal morula cell', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(137278, 'HP:0034322', 'Reduced galactocerebrosidase activity', 'XPO:0141797', 'abnormal hydrogen metabolic process', 0.5238095238095238, 4.758907843651163, 1.5788480773767701, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(137279, 'HP:0034322', 'Reduced galactocerebrosidase activity', 'XPO:0100225', 'abnormal endocrine system', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(137280, 'HP:0034322', 'Reduced galactocerebrosidase activity', 'XPO:0131745', 'abnormal axis elongation', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(137281, 'HP:0034322', 'Reduced galactocerebrosidase activity', 'XPO:0141883', 'abnormal glycerol metabolic process', 0.4230769230769231, 4.758907843651163, 1.418937661667548, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(137282, 'HP:0034322', 'Reduced galactocerebrosidase activity', 'XPO:0100232', 'abnormal lymphatic system', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(137283, 'HP:0034322', 'Reduced galactocerebrosidase activity', 'XPO:0141775', 'abnormal nitrogen compound metabolic process', 0.5238095238095238, 4.758907843651163, 1.5788480773767701, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(137284, 'HP:0034322', 'Reduced galactocerebrosidase activity', 'XPO:0101237', 'abnormal mucus secreting cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(137285, 'HP:0034322', 'Reduced galactocerebrosidase activity', 'XPO:0100026', 'abnormal germ cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(137286, 'HP:0034322', 'Reduced galactocerebrosidase activity', 'XPO:0100337', 'abnormal zygote', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(137287, 'HP:0034322', 'Reduced galactocerebrosidase activity', 'XPO:0141854', 'abnormal glutathione metabolic process', 0.4230769230769231, 4.758907843651163, 1.418937661667548, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(137288, 'HP:0034322', 'Reduced galactocerebrosidase activity', 'XPO:0141787', 'abnormal hormone metabolic process', 0.5238095238095238, 4.758907843651163, 1.5788480773767701, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(137289, 'HP:0034322', 'Reduced galactocerebrosidase activity', 'XPO:0101157', 'abnormal female organism', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(137290, 'HP:0034322', 'Reduced galactocerebrosidase activity', 'XPO:0133388', 'absent insulin receptor signaling pathway', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(137291, 'HP:0034322', 'Reduced galactocerebrosidase activity', 'XPO:0107259', 'abnormal animal-vegetal axis', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(137292, 'HP:0034322', 'Reduced galactocerebrosidase activity', 'XPO:0101132', 'abnormal apoptotic cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(137293, 'HP:0034322', 'Reduced galactocerebrosidase activity', 'XPO:0100010', 'abnormal multicellular anatomical structure', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(137294, 'HP:0034322', 'Reduced galactocerebrosidase activity', 'XPO:0100549', 'abnormal mitotic cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(137295, 'HP:0034322', 'Reduced galactocerebrosidase activity', 'XPO:0101061', 'abnormal plasma membrane', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(137296, 'HP:0034322', 'Reduced galactocerebrosidase activity', 'XPO:0131667', 'abnormal actin cytoskeleton', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(137297, 'HP:0034322', 'Reduced galactocerebrosidase activity', 'XPO:0141791', 'abnormal primary metabolic process', 0.5238095238095238, 4.758907843651163, 1.5788480773767701, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(137298, 'HP:0034322', 'Reduced galactocerebrosidase activity', 'XPO:0107284', 'abnormal migrating myoblast', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(137299, 'HP:0034322', 'Reduced galactocerebrosidase activity', 'XPO:0100674', 'abnormal secondary oogonium', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(137300, 'HP:0034322', 'Reduced galactocerebrosidase activity', 'XPO:0115505', 'dead whole organism', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(137301, 'HP:0034322', 'Reduced galactocerebrosidase activity', 'XPO:0141859', 'abnormal lactose catabolic process', 0.4230769230769231, 4.758907843651163, 1.418937661667548, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(137302, 'HP:0034322', 'Reduced galactocerebrosidase activity', 'XPO:0100976', 'abnormal multiciliated cell', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(137303, 'HP:0034322', 'Reduced galactocerebrosidase activity', 'XPO:0116434', 'abnormal biological process', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(137304, 'HP:0034322', 'Reduced galactocerebrosidase activity', 'XPO:0100515', 'abnormal somatic stem cell', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(137305, 'HP:0034322', 'Reduced galactocerebrosidase activity', 'XPO:0141267', 'abnormal resting posture', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(137306, 'HP:0034322', 'Reduced galactocerebrosidase activity', 'XPO:0141771', 'abnormal urea homeostasis', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(137307, 'HP:0034322', 'Reduced galactocerebrosidase activity', 'XPO:0131729', 'abnormal regulation of growth rate', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(137308, 'HP:0034322', 'Reduced galactocerebrosidase activity', 'XPO:0100239', 'abnormal acellular anatomical structure', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(137309, 'HP:0034322', 'Reduced galactocerebrosidase activity', 'XPO:0100728', 'abnormal cell condensation', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(137310, 'HP:0034322', 'Reduced galactocerebrosidase activity', 'XPO:0100317', 'abnormal respiratory system', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(137311, 'HP:0034322', 'Reduced galactocerebrosidase activity', 'XPO:0100481', 'abnormal anatomical line', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(137312, 'HP:0034322', 'Reduced galactocerebrosidase activity', 'XPO:0101141', 'abnormal Keller explant', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(137313, 'HP:0034322', 'Reduced galactocerebrosidase activity', 'XPO:0141788', 'abnormal hormone biosynthetic process', 0.44, 4.758907843651163, 1.447038165082909, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(137314, 'HP:0034322', 'Reduced galactocerebrosidase activity', 'XPO:0141776', 'abnormal metabolic process', 0.5789473684210527, 4.758907843651163, 1.6598666129060333, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(137315, 'HP:0034322', 'Reduced galactocerebrosidase activity', 'XPO:0100172', 'abnormal stem cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(137316, 'HP:0034322', 'Reduced galactocerebrosidase activity', 'XPO:0101467', 'abnormal alkali secreting cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(137317, 'HP:0034322', 'Reduced galactocerebrosidase activity', 'XPO:0141745', 'abnormal creatinine homeostasis', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(137318, 'HP:0034322', 'Reduced galactocerebrosidase activity', 'XPO:0115512', 'abnormally semi-erect whole organism', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(137319, 'HP:0034322', 'Reduced galactocerebrosidase activity', 'XPO:0101240', 'abnormal ciliated non-epidermal cell', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(137320, 'HP:0034322', 'Reduced galactocerebrosidase activity', 'XPO:0101409', 'abnormal perivitelline space', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(137321, 'HP:0034322', 'Reduced galactocerebrosidase activity', 'XPO:0101547', 'abnormal lampbrush chromosome', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(137322, 'HP:0034322', 'Reduced galactocerebrosidase activity', 'XPO:0141784', 'abnormal cellular hormone metabolic process', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(137323, 'HP:0034322', 'Reduced galactocerebrosidase activity', 'XPO:0141881', 'abnormal fructose metabolic process', 0.4230769230769231, 4.758907843651163, 1.418937661667548, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(137324, 'HP:0034322', 'Reduced galactocerebrosidase activity', 'XPO:0131469', 'abnormal heart process', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(137325, 'HP:0034322', 'Reduced galactocerebrosidase activity', 'XPO:0101435', 'abnormal paracrine cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(137326, 'HP:0034322', 'Reduced galactocerebrosidase activity', 'XPO:0100573', 'abnormal extraembryonic structure', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(137327, 'HP:0034322', 'Reduced galactocerebrosidase activity', 'XPO:0100308', 'abnormal early embryonic cell', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
