(288877, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0101576', 'abnormal blastomere V1.2.2', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(288878, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0101200', 'abnormal joint region', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(288879, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0131523', 'absent actin filament', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(288880, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0131351', 'abnormally decreased number of apoptotic cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(288881, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0127819', 'abnormally localised ciliary axoneme', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(288882, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0100415', 'abnormal secretory epithelial cell', 0.52, 3.6715585125471644, 1.3817418089225373, 'UPHENO:0086172', 'abnormal cell'),
(288883, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0100477', 'abnormal pericyte', 0.6190476190476191, 3.6715585125471644, 1.5076039119696991, 'UPHENO:0086172', 'abnormal cell'),
(288884, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0107271', 'abnormal apical region', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(288885, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0100573', 'abnormal extraembryonic structure', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(288886, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0102353', 'abnormal centromere morphology', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(288887, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0127337', 'abnormally localised oxygen accumulating cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(288888, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0101168', 'abnormal circulating cell', 0.52, 3.6715585125471644, 1.3817418089225373, 'UPHENO:0086172', 'abnormal cell'),
(288889, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0124864', 'absent germ cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(288890, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0126725', 'abnormally localised epithelial cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(288891, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0131550', 'abnormally localised adherens junction', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(288892, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0101535', 'abnormal absorptive cell', 0.6190476190476191, 3.6715585125471644, 1.5076039119696991, 'UPHENO:0086172', 'abnormal cell'),
(288893, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0101192', 'abnormal blastomere D2.1', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(288894, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0131032', 'abnormally increased number of acid secreting cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(288895, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0102526', 'abnormal nucleus morphology', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(288896, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0115758', 'abnormally decreased mobility of melanoblast', 0.52, 3.6715585125471644, 1.3817418089225373, 'UPHENO:0086172', 'abnormal cell'),
(288897, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0131677', 'abnormal actin filament', 0.5652173913043478, 3.6715585125471644, 1.440565418328227, 'UPHENO:0086172', 'abnormal cell'),
(288898, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0127896', 'abnormally localised ring structure', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(288899, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0101969', 'abnormal zygote morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(288900, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0101366', 'abnormal morula cell', 0.5652173913043478, 3.6715585125471644, 1.440565418328227, 'UPHENO:0086172', 'abnormal cell'),
(288901, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0101484', 'abnormal bone marrow', 0.43333333333333335, 5.574066539846944, 1.5541649957239663, 'UPHENO:0004459', 'abnormal hematopoietic system'),
(288902, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0101921', 'abnormal chondroblast morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(288903, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0100546', 'abnormal whole organism', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(288904, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0103067', 'abnormal paracrine cell morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(288905, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0103636', 'abnormally increased number of melanoblast', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(288906, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0100862', 'abnormal blastomere V1', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(288907, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0126314', 'absent absorptive cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(288908, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0133436', 'abnormal cilium morphology in the multiciliated cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(288909, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0131189', 'abnormally decreased number of stem cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(288910, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0102147', 'abnormal somatic stem cell morphology', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(288911, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0125530', 'absent chondroblast', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(288912, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0100872', 'abnormal neuroendocrine cell', 0.48148148148148145, 3.6715585125471644, 1.3295816755533123, 'UPHENO:0086172', 'abnormal cell'),
(288913, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0124884', 'absent keratin accumulating cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(288914, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0102165', 'abnormal melanoblast morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(288915, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0101078', 'abnormal mucous gland', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(288916, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0103082', 'abnormal myeloid cell morphology', 0.4411764705882353, 5.574066539846944, 1.568166765007361, 'HP:0001871', 'Abnormality of blood and blood-forming tissues'),
(288917, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0100674', 'abnormal secondary oogonium', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(288918, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0115391', 'abnormally undifferentiated alimentary system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(288919, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0127774', 'abnormally localised hemangioblast', 0.46875, 5.574066539846944, 1.6164293026771246, 'HP:0001871', 'Abnormality of blood and blood-forming tissues'),
(288920, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0131735', 'abnormal spindle assembly', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(288921, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0102588', 'abnormal centrosome morphology', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(288922, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0101480', 'abnormal stage V oocyte', 0.5652173913043478, 3.6715585125471644, 1.440565418328227, 'UPHENO:0086172', 'abnormal cell'),
(288923, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0141265', 'abnormal escape behavior', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(288924, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0131145', 'abnormally increased number of polar body', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(288925, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0101269', 'abnormal mesodermal cell', 0.48148148148148145, 3.6715585125471644, 1.3295816755533123, 'UPHENO:0086172', 'abnormal cell'),
(288926, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0101278', 'abnormal pigment cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(288927, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0100861', 'abnormal blastomere D2.2.2', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(288928, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0100069', 'abnormal urinary system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(288929, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0102061', 'abnormal spermatid morphology', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(288930, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0102739', 'abnormal erythroid cell morphology', 0.4411764705882353, 5.574066539846944, 1.568166765007361, 'HP:0001871', 'Abnormality of blood and blood-forming tissues'),
(288931, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0141718', 'abnormal posterior notochord', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(288932, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0141796', 'abnormal demethylation', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(288933, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0141266', 'abnormal surface breathing', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(288934, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0103219', 'abnormal hemangioblast morphology', 0.4411764705882353, 5.574066539846944, 1.568166765007361, 'UPHENO:0004459', 'abnormal hematopoietic system'),
(288935, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0124807', 'absent cell part', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(288936, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0101636', 'abnormal cell morphology', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(288937, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0131204', 'abnormally decreased number of pericyte', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(288938, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0101009', 'abnormal blastomere D1.1.1', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(288939, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0100458', 'abnormal autopod', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(288940, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0100742', 'abnormal musculoskeletal system', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(288941, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0101311', 'abnormal bottle cell', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(288942, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0133438', 'abnormal cilium morphology in the ciliated non-epidermal cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(288943, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0100902', 'abnormal spermatocyte', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(288944, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0131171', 'abnormally increased number of barrier epithelial cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(288945, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0101448', 'abnormal myelin accumulating cell', 0.6190476190476191, 3.6715585125471644, 1.5076039119696991, 'UPHENO:0086172', 'abnormal cell'),
(288946, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0100218', 'abnormal epithelial cell', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(288947, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0100570', 'abnormal axon', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(288948, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0115615', 'abnormally posteriorly mislocalised primordial germ cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(288949, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0100823', 'abnormal blood', 0.5416666666666666, 5.574066539846944, 1.737609289344729, 'UPHENO:0004459', 'abnormal hematopoietic system'),
(288950, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0131371', 'abnormally decreased number of electrically active cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(288951, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0102768', 'abnormal ooplasm morphology', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(288952, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0107253', 'abnormal enteric nervous system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(288953, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0141511', 'abnormally localised nucleus in myoblast', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(288954, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0141776', 'abnormal metabolic process', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(288955, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0100901', 'abnormal blastomere D1.2.2', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(288956, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0141791', 'abnormal primary metabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(288957, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0130964', 'abnormally increased number of cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(288958, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0100268', 'abnormal circulatory system', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(288959, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0100337', 'abnormal zygote', 0.6190476190476191, 3.6715585125471644, 1.5076039119696991, 'UPHENO:0086172', 'abnormal cell'),
(288960, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0102455', 'abnormal blood morphology', 0.41935483870967744, 5.574066539846944, 1.5288923359002506, 'UPHENO:0004459', 'abnormal hematopoietic system'),
(288961, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0100009', 'abnormal multi-tissue structure', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(288962, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0127876', 'abnormally localised microtubule', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(288963, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0141264', 'abnormal schooling behavior', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(288964, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0101740', 'abnormal cell part morphology', 0.48148148148148145, 3.6715585125471644, 1.3295816755533123, 'UPHENO:0086172', 'abnormal cell'),
(288965, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0101188', 'abnormal posterior ventral blood island', 0.4642857142857143, 5.574066539846944, 1.6087136056268494, 'UPHENO:0004459', 'abnormal hematopoietic system'),
(288966, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0127171', 'abnormally localised myelin accumulating cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(288967, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0141738', 'abnormal carbon dioxide homeostasis', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(288968, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0101327', 'abnormal blastomere V1.2.1', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(288969, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0107263', 'abnormal anatomical side', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(288970, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0101504', 'abnormal blastomere D2.2.1', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(288971, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0131090', 'abnormally increased number of oxygen accumulating cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(288972, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0101358', 'abnormal endothelial cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(288973, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0100654', 'abnormal blastomere V2.1', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(288974, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0102386', 'abnormal electrically active cell morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(288975, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0107259', 'abnormal animal-vegetal axis', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(288976, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0107311', 'abnormal apical junction complex', 0.5, 3.6715585125471644, 1.3549093166236559, 'UPHENO:0086172', 'abnormal cell'),
(288977, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0100691', 'abnormal keratin accumulating cell', 0.6190476190476191, 3.6715585125471644, 1.5076039119696991, 'UPHENO:0086172', 'abnormal cell'),
(288978, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0100422', 'abnormal notochord', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(288979, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0126630', 'abnormally localised early embryonic cell', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(288980, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0128071', 'decreased size of the cell part', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(288981, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0131278', 'abnormally decreased number of keratin accumulating cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(288982, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0100728', 'abnormal cell condensation', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(288983, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0131383', 'abnormally decreased number of cementoblast', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(288984, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0102873', 'abnormal nucleate erythrocyte morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(288985, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0131031', 'abnormally increased number of nucleate erythrocyte', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(288986, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0100232', 'abnormal lymphatic system', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(288987, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0127837', 'abnormally localised erythroid cell', 0.46875, 5.574066539846944, 1.6164293026771246, 'HP:0001871', 'Abnormality of blood and blood-forming tissues'),
(288988, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0126388', 'abnormally localised oocyte', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(288989, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0100186', 'abnormal uveal tract', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(288990, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0100814', 'abnormal natural killer cell', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(288991, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0141784', 'abnormal cellular hormone metabolic process', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(288992, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0100070', 'abnormal anatomical system', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(288993, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0100599', 'abnormal adult immune system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(288994, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0141314', 'abnormal Roux spot morphology', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(288995, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0100587', 'abnormal vestibuloauditory system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(288996, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0101133', 'abnormal motor neuron', 0.48148148148148145, 3.6715585125471644, 1.3295816755533123, 'UPHENO:0086172', 'abnormal cell'),
(288997, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0100701', 'abnormal microglial cell', 0.48148148148148145, 3.6715585125471644, 1.3295816755533123, 'UPHENO:0086172', 'abnormal cell'),
(288998, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0101405', 'abnormal ring structure', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(288999, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0131314', 'abnormally decreased number of exocrine cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(289000, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0101221', 'abnormal larval immune system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(289001, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0100034', 'abnormal blastomere V1.1', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(289002, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0125384', 'absent ciliated cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(289003, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0103104', 'abnormal zygote cortex morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(289004, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0126671', 'abnormally localised zygote', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(289005, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0100610', 'abnormal appendage', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289006, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0131180', 'abnormally decreased number of cell', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(289007, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0141786', 'abnormal pigment metabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(289008, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0125577', 'absent cilium', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(289009, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0131667', 'abnormal actin cytoskeleton', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(289010, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0102285', 'abnormal myoblast morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(289011, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0131666', 'abnormal adherens junction', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(289012, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0101461', 'abnormal sperm entry point', 0.5652173913043478, 3.6715585125471644, 1.440565418328227, 'UPHENO:0086172', 'abnormal cell'),
(289013, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0141794', 'abnormal prosthetic group metabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(289014, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0100673', 'abnormal anterior dorsal lateral plate region', 0.41935483870967744, 5.574066539846944, 1.5288923359002506, 'UPHENO:0004459', 'abnormal hematopoietic system'),
(289015, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0100888', 'abnormal microtubule', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(289016, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0126738', 'abnormally localised paracrine cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(289017, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0100384', 'abnormal amputated tissue', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289018, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0101113', 'abnormal stage IV oocyte', 0.5652173913043478, 3.6715585125471644, 1.440565418328227, 'UPHENO:0086172', 'abnormal cell'),
(289019, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0102181', 'abnormal mitotic cell morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(289020, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0125750', 'absent melanoblast', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(289021, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0126413', 'abnormally localised cell part', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(289022, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0100596', 'abnormal myocyte', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(289023, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0100317', 'abnormal respiratory system', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(289024, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0101074', 'abnormal germinal vesicle', 0.52, 3.6715585125471644, 1.3817418089225373, 'UPHENO:0086172', 'abnormal cell'),
(289025, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0107284', 'abnormal migrating myoblast', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(289026, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0141782', 'abnormal methylation', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(289027, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0141271', 'increased surface breathing', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(289028, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0125135', 'absent blood', 0.40625, 5.574066539846944, 1.5048137864243607, 'HP:0001871', 'Abnormality of blood and blood-forming tissues'),
(289029, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0100202', 'abnormal embryo', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289030, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0131553', 'abnormally localised Roux spot', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(289031, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0141276', 'decreased surface breathing', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(289032, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0102336', 'abnormal Merkel cell morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(289033, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0130988', 'abnormally increased number of pericyte', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(289034, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0102306', 'abnormal secondary oogonium morphology', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(289035, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0130986', 'abnormally increased number of germ cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(289036, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0102869', 'abnormal mucus secreting cell morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(289037, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0107276', 'abnormal dorsal region', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289038, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0101452', 'abnormal blastomere V1.1.1', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(289039, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0101406', 'abnormal cleavage furrow', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289040, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0100675', 'abnormal dorsal vegetal hemisphere blastomere', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(289041, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0107268', 'abnormal left side', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289042, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0126783', 'abnormally localised exocrine cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(289043, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0131308', 'abnormally decreased number of oxygen accumulating cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(289044, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0100004', 'abnormal cell', 0.65, 3.6715585125471644, 1.5448343060521594, 'UPHENO:0086172', 'abnormal cell'),
(289045, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0127806', 'abnormally localised spermatid', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(289046, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0126537', 'abnormally localised hematological system', 0.41935483870967744, 5.574066539846944, 1.5288923359002506, 'HP:0001871', 'Abnormality of blood and blood-forming tissues'),
(289047, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0100852', 'abnormal interdigital region', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(289048, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0102958', 'abnormal cementoblast morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(289049, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0131346', 'abnormally decreased number of chondroblast', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(289050, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0100917', 'abnormal stage III oocyte', 0.5652173913043478, 3.6715585125471644, 1.440565418328227, 'UPHENO:0086172', 'abnormal cell'),
(289051, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0102069', 'abnormal proepicardium morphology', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(289052, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0100251', 'abnormal proteinaceous extracellular matrix', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289053, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0126183', 'absent myeloid cell', 0.4411764705882353, 5.574066539846944, 1.568166765007361, 'UPHENO:0004459', 'abnormal hematopoietic system'),
(289054, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0102520', 'abnormal microtubule morphology', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(289055, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0102534', 'abnormal spermatocyte morphology', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(289056, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0141781', 'abnormal secondary metabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(289057, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0125013', 'absent early embryonic cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(289058, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0126983', 'abnormally localised primordial germ cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(289059, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0100781', 'abnormal presumptive ectoderm', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289060, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0101023', 'abnormal ultimobranchial body', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(289061, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0103145', 'abnormal basal body morphology', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(289062, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0102764', 'abnormal apoptotic cell morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(289063, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0101071', 'abnormal endoplasmic reticulum', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(289064, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0101373', 'abnormal oxygen accumulating cell', 0.6190476190476191, 3.6715585125471644, 1.5076039119696991, 'UPHENO:0086172', 'abnormal cell'),
(289065, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0142065', 'abnormally decreased number of desmosome', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(289066, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0107261', 'abnormal dorsal-ventral axis', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289067, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0100520', 'abnormal blastomere D1.2', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(289068, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0100274', 'abnormal sensory system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(289069, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0101302', 'abnormal subcortical cytoplasm', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(289070, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0100842', 'abnormal left-dorsal blastomere', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(289071, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0125859', 'absent nucleate erythrocyte', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(289072, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0127160', 'abnormally localised acid secreting cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(289073, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0127018', 'abnormally localised ciliated cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(289074, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0101575', 'abnormal vitelline membrane', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(289075, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0131141', 'abnormally increased number of hemangioblast', 0.4411764705882353, 5.574066539846944, 1.568166765007361, 'HP:0001871', 'Abnormality of blood and blood-forming tissues'),
(289076, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0141267', 'abnormal resting posture', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(289077, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0102693', 'abnormal plasma membrane morphology', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(289078, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0101494', 'abnormal blastomere D1.2.1', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(289079, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0100308', 'abnormal early embryonic cell', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(289080, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0141748', 'abnormal gas homeostasis', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(289081, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0100427', 'abnormal olfactory system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(289082, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0101109', 'abnormal egg cell-free extract', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289083, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0100967', 'abnormal blastomere V2.1.2', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(289084, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0127533', 'abnormally localised spermatocyte', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(289085, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0101004', 'abnormal acid secreting cell', 0.6190476190476191, 3.6715585125471644, 1.5076039119696991, 'UPHENO:0086172', 'abnormal cell'),
(289086, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0127339', 'abnormally localised migrating myoblast', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(289087, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0131004', 'abnormally increased number of proepicardium', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(289088, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0141772', 'abnormal water homeostasis', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(289089, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0101547', 'abnormal lampbrush chromosome', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(289090, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0100316', 'abnormal gamete', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(289091, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0100372', 'abnormal hematological system', 0.5909090909090909, 5.574066539846944, 1.8148737123358583, 'UPHENO:0004459', 'abnormal hematopoietic system'),
(289092, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0101110', 'abnormal cell-free extract', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289093, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0100152', 'abnormal alimentary system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(289094, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0131337', 'abnormally decreased number of erythroid cell', 0.42857142857142855, 5.574066539846944, 1.5456020380209146, 'UPHENO:0004459', 'abnormal hematopoietic system'),
(289095, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0141498', 'abnormal axon microtubule bundle', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(289096, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0131082', 'abnormally increased number of alkali secreting cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(289097, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0100396', 'abnormal dorsal animal hemisphere blastomere', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(289098, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0127643', 'abnormally localised somatic stem cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(289099, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0141263', 'abnormal visually guided collision avoidance behavior', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(289100, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0125394', 'absent multiciliated cell precursor', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(289101, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0100025', 'abnormal oocyte', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(289102, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0107312', 'abnormal filopodium', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(289103, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0133443', 'abnormally increased number of cilium in the multiciliated cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(289104, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0125724', 'absent polar body', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(289105, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0100423', 'abnormal process', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289106, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0101472', 'abnormal zygote cortex', 0.5652173913043478, 3.6715585125471644, 1.440565418328227, 'UPHENO:0086172', 'abnormal cell'),
(289107, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0101157', 'abnormal female organism', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289108, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0101490', 'abnormal ectodermal cell', 0.48148148148148145, 3.6715585125471644, 1.3295816755533123, 'UPHENO:0086172', 'abnormal cell'),
(289109, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0100549', 'abnormal mitotic cell', 0.6190476190476191, 3.6715585125471644, 1.5076039119696991, 'UPHENO:0086172', 'abnormal cell'),
(289110, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0127288', 'abnormally localised pericyte', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(289111, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0125693', 'absent mucus secreting cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(289112, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0126159', 'absent apoptotic cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(289113, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0100676', 'abnormal blastomere D2.2', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(289114, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0141714', 'abnormal anterior notochord', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(289115, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0101534', 'abnormal blastomere V2.1.1', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(289116, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0101498', 'abnormal stage II oocyte', 0.5652173913043478, 3.6715585125471644, 1.440565418328227, 'UPHENO:0086172', 'abnormal cell'),
(289117, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0125715', 'absent barrier cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(289118, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0100501', 'abnormal urogenital system', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(289119, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0103099', 'abnormal alkali secreting cell morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(289120, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0101297', 'abnormal barrier cell', 0.6190476190476191, 3.6715585125471644, 1.5076039119696991, 'UPHENO:0086172', 'abnormal cell'),
(289121, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0101283', 'abnormal left-ventral blastomere', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(289122, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0100721', 'abnormal centromere', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(289123, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0102703', 'abnormal endoplasmic reticulum morphology', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(289124, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0131512', 'absent adherens junction', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(289125, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0115512', 'abnormally semi-erect whole organism', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289126, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0127653', 'abnormally localised Merkel cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(289127, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0141777', 'abnormal catabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(289128, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0101519', 'abnormal hypobranchial placode', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289129, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0103167', 'abnormal absorptive cell morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(289130, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0101162', 'abnormal stromal cell', 0.48148148148148145, 3.6715585125471644, 1.3295816755533123, 'UPHENO:0086172', 'abnormal cell'),
(289131, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0101176', 'abnormal non-ciliated epithelial cell', 0.52, 3.6715585125471644, 1.3817418089225373, 'UPHENO:0086172', 'abnormal cell'),
(289132, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0100989', 'abnormal right blastomere', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(289133, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0141715', 'abnormal septum', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289134, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0100404', 'abnormal hematopoietic stem cell', 0.42857142857142855, 5.574066539846944, 1.5456020380209146, 'HP:0001871', 'Abnormality of blood and blood-forming tissues'),
(289135, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0103414', 'abnormally increased number of vacuole in the spermatozoon', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(289136, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0115509', 'abnormally semi-viable whole organism', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289137, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0126506', 'abnormally localised thrombocyte', 0.4166666666666667, 5.574066539846944, 1.523984161642183, 'UPHENO:0004459', 'abnormal hematopoietic system'),
(289138, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0100915', 'abnormal dermal system', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289139, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0100289', 'abnormal chondroblast', 0.6190476190476191, 3.6715585125471644, 1.5076039119696991, 'UPHENO:0086172', 'abnormal cell'),
(289140, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0127029', 'abnormally localised multiciliated cell precursor', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(289141, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:00000000', 'Xenopus phenotype', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(289142, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0127428', 'abnormally localised endoplasmic reticulum', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(289143, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0101212', 'abnormal glomeral mesenchyme', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(289144, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0101120', 'abnormal cardiac progenitor cell', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(289145, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0141743', 'abnormal chemical homeostasis within a tissue', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(289146, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0100344', 'abnormal portion of organism substance', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289147, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0100733', 'abnormal fibroblast', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(289148, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0100762', 'abnormal intersomitic region', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289149, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0102994', 'abnormal vegetal cortex morphology', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(289150, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0131706', 'abnormal ciliary basal body organization', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(289151, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0100114', 'abnormal peripheral nervous system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(289152, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0100273', 'abnormal visual system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(289153, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0131292', 'abnormally decreased number of mucus secreting cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(289154, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0127975', 'abnormally localised mitochondrial cloud', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(289155, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0101411', 'abnormal marginal zone (sensu neural)', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289156, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0127343', 'abnormally localised filopodium', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(289157, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0107258', 'abnormal anatomical axis', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289158, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0131669', 'abnormal Roux spot', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(289159, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0100643', 'abnormal thoracic region', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289160, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0101518', 'abnormal B cell', 0.48148148148148145, 3.6715585125471644, 1.3295816755533123, 'UPHENO:0086172', 'abnormal cell'),
(289161, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0101237', 'abnormal mucus secreting cell', 0.6190476190476191, 3.6715585125471644, 1.5076039119696991, 'UPHENO:0086172', 'abnormal cell'),
(289162, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0100745', 'abnormal anterior lymph sac', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(289163, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0116091', 'abnormally increased variability of size of cell in endoderm', 0.48148148148148145, 3.6715585125471644, 1.3295816755533123, 'UPHENO:0086172', 'abnormal cell'),
(289164, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0102965', 'abnormal barrier epithelial cell morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(289165, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0107254', 'abnormal neutrophil', 0.46875, 5.574066539846944, 1.6164293026771246, 'HP:0001871', 'Abnormality of blood and blood-forming tissues'),
(289166, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0101333', 'abnormal barrier epithelial cell', 0.6190476190476191, 3.6715585125471644, 1.5076039119696991, 'UPHENO:0086172', 'abnormal cell'),
(289167, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0102636', 'abnormal acid secreting cell morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(289168, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0101374', 'abnormal migratory neural crest cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(289169, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0141289', 'abnormal spindle microtubule morphology', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(289170, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0126758', 'abnormally localised blood', 0.41935483870967744, 5.574066539846944, 1.5288923359002506, 'HP:0001871', 'Abnormality of blood and blood-forming tissues'),
(289171, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0100239', 'abnormal acellular anatomical structure', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289172, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0125692', 'absent oxygen accumulating cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(289173, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0141778', 'abnormal biosynthetic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(289174, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0141797', 'abnormal hydrogen metabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(289175, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0100913', 'abnormal Brachets cleft', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289176, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0100515', 'abnormal somatic stem cell', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(289177, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0100437', 'abnormal proepicardium', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(289178, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0101228', 'abnormal mesenchymal stem cell', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(289179, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0100216', 'abnormal hepato-pancreatic progenitor cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(289180, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0125698', 'absent filopodium', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(289181, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0100882', 'abnormal perichondrial cell', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(289182, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0125644', 'absent pericyte', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(289183, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0101264', 'abnormal mitotic spindle', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(289184, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0101202', 'abnormal thymus', 0.41935483870967744, 5.574066539846944, 1.5288923359002506, 'HP:0001871', 'Abnormality of blood and blood-forming tissues'),
(289185, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0102434', 'abnormal exocrine cell morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(289186, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0103093', 'abnormal sperm entry point morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(289187, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0100481', 'abnormal anatomical line', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289188, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0131300', 'abnormally decreased number of alkali secreting cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(289189, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0101061', 'abnormal plasma membrane', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(289190, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0130989', 'abnormally increased number of ciliated cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(289191, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0100026', 'abnormal germ cell', 0.6190476190476191, 3.6715585125471644, 1.5076039119696991, 'UPHENO:0086172', 'abnormal cell'),
(289192, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0131248', 'abnormally decreased number of acid secreting cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(289193, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0125833', 'absent kinetochore', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(289194, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0100398', 'abnormal vegetal blastomere', 0.48148148148148145, 3.6715585125471644, 1.3295816755533123, 'UPHENO:0086172', 'abnormal cell'),
(289195, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0101515', 'abnormal neuromast mantle cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(289196, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0101409', 'abnormal perivitelline space', 0.5652173913043478, 3.6715585125471644, 1.440565418328227, 'UPHENO:0086172', 'abnormal cell'),
(289197, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0131307', 'abnormally decreased number of mitotic cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(289198, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0100912', 'abnormal trabecula', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289199, 'HP:0001872', 'Abnormality of thrombocytes', 'XPO:0131297', 'abnormally decreased number of melanoblast', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(289200, 'HP:0040046', 'Abnormal left hemidiaphragm morphology', 'XPO:0101732', 'abnormal muscle morphology', 0.40476190476190477, 6.895202660022325, 1.6706032929423995, 'HP:0011805', 'Abnormal skeletal muscle morphology'),
(289201, 'HP:0040046', 'Abnormal left hemidiaphragm morphology', 'XPO:0100317', 'abnormal respiratory system', 0.41935483870967744, 6.780552239366747, 1.6862554345953, 'UPHENO:0004536', 'abnormal respiratory system'),
(289202, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100917', 'abnormal stage III oocyte', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(289203, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0101857', 'abnormal endocrine system morphology', 0.41935483870967744, 6.2194654996189955, 1.6149807898093176, 'UPHENO:0003116', 'abnormal endocrine system'),
(289204, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0101976', 'abnormal portion of organism substance morphology', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289205, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0131687', 'abnormal astral microtubule', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(289206, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100261', 'abnormal multilaminar epithelium', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289207, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100509', 'abnormal germ plasm', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(289208, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0141267', 'abnormal resting posture', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(289209, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100133', 'abnormal solid compound organ', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289210, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0107260', 'abnormal anterior-posterior axis', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289211, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0101029', 'abnormal right spleen primordium', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(289212, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100916', 'abnormal principal cavity', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(289213, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100642', 'abnormal gustatory system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(289214, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100386', 'abnormal limb', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(289215, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0141315', 'abnormal anatomical region', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289216, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0107261', 'abnormal dorsal-ventral axis', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289217, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100415', 'abnormal secretory epithelial cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(289218, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0101136', 'abnormal ooplasm', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(289219, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0131691', 'abnormal molecular function', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(289220, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100605', 'abnormal prechordal plate', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289221, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0101023', 'abnormal ultimobranchial body', 0.5416666666666666, 6.2194654996189955, 1.835450120713433, 'UPHENO:0003116', 'abnormal endocrine system'),
(289222, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0101362', 'abnormal vegetal cortex', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(289223, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0101010', 'abnormal dorsal marginal zone', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289224, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100612', 'abnormal unilaminar epithelium', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289225, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100956', 'abnormal centrosome', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(289226, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100638', 'abnormal polar body', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(289227, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100023', 'abnormal mesenchyme', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289228, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0115758', 'abnormally decreased mobility of melanoblast', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(289229, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100449', 'abnormal lymphocyte', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(289230, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100002', 'abnormal head', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(289231, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100999', 'abnormal serous membrane', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289232, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0101072', 'abnormal mitochondrial cloud', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(289233, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100296', 'abnormal tail region', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289234, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100991', 'abnormal iliac process primordium', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289235, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100807', 'abnormal matrix-based tissue', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289236, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0141715', 'abnormal septum', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289237, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0141776', 'abnormal metabolic process', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(289238, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100009', 'abnormal multi-tissue structure', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289239, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100816', 'abnormal blastocoel anlage', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289240, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0141786', 'abnormal pigment metabolic process', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(289241, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0101113', 'abnormal stage IV oocyte', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(289242, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100860', 'abnormal parathyroid', 0.5, 6.2194654996189955, 1.763443435386998, 'UPHENO:0003116', 'abnormal endocrine system'),
(289243, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0101004', 'abnormal acid secreting cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(289244, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0141718', 'abnormal posterior notochord', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(289245, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100537', 'abnormal medium cavity', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(289246, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0141781', 'abnormal secondary metabolic process', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(289247, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100192', 'abnormal epithelium', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289248, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100256', 'abnormal paired appendage', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289249, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:00000000', 'Xenopus phenotype', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(289250, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0131725', 'abnormal phosphorylation of RNA polymerase II C-terminal domain', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(289251, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100196', 'abnormal neuron', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(289252, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0101061', 'abnormal plasma membrane', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(289253, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0131685', 'abnormal cortical actin cytoskeleton', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(289254, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100114', 'abnormal peripheral nervous system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(289255, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0142054', 'abnormal digestive tract', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(289256, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0141770', 'abnormal urate homeostasis', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(289257, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0101713', 'abnormal anatomical entity in vitro morphology', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289258, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100858', 'abnormal presumptive midbrain-hindbrain boundary', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(289259, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100688', 'abnormal adipose tissue', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(289260, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100643', 'abnormal thoracic region', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289261, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100784', 'abnormal left blastomere', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(289262, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0141629', 'metaplastic thyroid', 0.43333333333333335, 6.2194654996189955, 1.6416764956901726, 'UPHENO:0003116', 'abnormal endocrine system'),
(289263, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0141790', 'abnormal cellular metabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(289264, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100802', 'abnormal exocrine cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(289265, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0101405', 'abnormal ring structure', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(289266, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100307', 'abnormal blastomere', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(289267, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0142057', 'abnormal desmosome', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(289268, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0107285', 'abnormal flexural organ', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(289269, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0101132', 'abnormal apoptotic cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(289270, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100067', 'abnormal animal hemisphere', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289271, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100437', 'abnormal proepicardium', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(289272, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100503', 'abnormal blastomere D2', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(289273, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0107270', 'abnormal proximal-distal axis', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289274, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0101448', 'abnormal myelin accumulating cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(289275, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0131677', 'abnormal actin filament', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(289276, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100377', 'abnormal connective tissue', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(289277, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100786', 'abnormal presumptive axial mesoderm', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289278, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0101373', 'abnormal oxygen accumulating cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(289279, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100715', 'abnormal ciliated cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(289280, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100468', 'abnormal muscular system', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289281, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100337', 'abnormal zygote', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(289282, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100691', 'abnormal keratin accumulating cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(289283, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0101543', 'abnormal external gill', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(289284, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0107264', 'abnormal anterior side', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289285, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100852', 'abnormal interdigital region', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(289286, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0101228', 'abnormal mesenchymal stem cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(289287, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0107262', 'abnormal left-right axis', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289288, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0141497', 'abnormal lymphoblast', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(289289, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0141272', 'absent surface breathing', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(289290, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100728', 'abnormal cell condensation', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289291, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0101220', 'abnormal centriole', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(289292, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0101176', 'abnormal non-ciliated epithelial cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(289293, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0101409', 'abnormal perivitelline space', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(289294, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0101435', 'abnormal paracrine cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(289295, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0101110', 'abnormal cell-free extract', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289296, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100363', 'abnormal cardiovascular system', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289297, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0141904', 'abnormal glucosamine metabolic process', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(289298, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100585', 'abnormal elastica externa', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(289299, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0107268', 'abnormal left side', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289300, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0141271', 'increased surface breathing', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(289301, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100189', 'abnormal enteroendocrine cell', 0.5, 6.2194654996189955, 1.763443435386998, 'UPHENO:0003116', 'abnormal endocrine system'),
(289302, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0101090', 'abnormal adrenal gland', 0.4642857142857143, 6.2194654996189955, 1.6992966138864523, 'UPHENO:0003116', 'abnormal endocrine system'),
(289303, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100010', 'abnormal multicellular anatomical structure', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289304, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100239', 'abnormal acellular anatomical structure', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289305, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0141745', 'abnormal creatinine homeostasis', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(289306, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0101547', 'abnormal lampbrush chromosome', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(289307, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100032', 'abnormal nervous system', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(289308, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100422', 'abnormal notochord', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(289309, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0101497', 'abnormal ciliary axoneme', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(289310, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0131669', 'abnormal Roux spot', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(289311, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100868', 'abnormal transporting epithelium', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289312, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100084', 'abnormal anatomical group', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289313, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0107269', 'abnormal right side', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289314, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0101503', 'abnormal organ cortex', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289315, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0101099', 'abnormal ventro-lateral marginal zone', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289316, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100203', 'abnormal endocrine cell', 0.52, 6.2194654996189955, 1.7983664976310803, 'UPHENO:0003116', 'abnormal endocrine system'),
(289317, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100501', 'abnormal urogenital system', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(289318, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0101519', 'abnormal hypobranchial placode', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289319, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0101535', 'abnormal absorptive cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(289320, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100477', 'abnormal pericyte', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(289321, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0101560', 'abnormal compound organ component', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289322, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0107311', 'abnormal apical junction complex', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(289323, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100384', 'abnormal amputated tissue', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289324, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100762', 'abnormal intersomitic region', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289325, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100856', 'abnormal simple organ', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289326, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0141783', 'abnormal collagen metabolic process', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(289327, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100976', 'abnormal multiciliated cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(289328, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0107288', 'abnormal larval alimentary system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(289329, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100887', 'abnormal right-dorsal blastomere', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(289330, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0101424', 'abnormal coelomic epithelium', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289331, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0101389', 'abnormal wedge region', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(289332, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100827', 'abnormal atypical epithelium', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289333, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100429', 'abnormal spermatid', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(289334, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100721', 'abnormal centromere', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(289335, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100285', 'abnormal progenitor cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(289336, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0107276', 'abnormal dorsal region', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289337, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100186', 'abnormal uveal tract', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289338, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0141266', 'abnormal surface breathing', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(289339, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100481', 'abnormal anatomical line', 0.5294117647058824, 1.706362323152461, 0.9504568842024205, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289340, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100309', 'abnormal vegetal hemisphere', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289341, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100417', 'abnormal dense regular connective tissue', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(289342, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0141771', 'abnormal urea homeostasis', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(289343, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100890', 'abnormal pharyngeal cavity', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(289344, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0101569', 'abnormal activin-induced ectoderm', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289345, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100025', 'abnormal oocyte', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(289346, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0107263', 'abnormal anatomical side', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289347, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0141738', 'abnormal carbon dioxide homeostasis', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(289348, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100626', 'abnormal primordial germ cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(289349, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0101174', 'abnormal articular system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(289350, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100902', 'abnormal spermatocyte', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(289351, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100707', 'abnormal central vegetal yolk mass', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289352, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100201', 'abnormal cavitated compound organ', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289353, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0107265', 'abnormal posterior side', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289354, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100546', 'abnormal whole organism', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289355, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100667', 'abnormal vegetal yolk mass', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289356, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0107267', 'abnormal ventral side', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289357, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100843', 'abnormal fasciculated network of fibrils', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(289358, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0142056', 'abnormal main body axis', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289359, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0101577', 'abnormal notochordal epithelium', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289360, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0115505', 'dead whole organism', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289361, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100653', 'abnormal myoblast', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(289362, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0101237', 'abnormal mucus secreting cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(289363, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0141499', 'abnormal tadpole', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289364, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100573', 'abnormal extraembryonic structure', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289365, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100164', 'abnormal neural nucleus', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(289366, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100339', 'abnormal circumblastoporal collar', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289367, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100915', 'abnormal dermal system', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289368, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100344', 'abnormal portion of organism substance', 0.5294117647058824, 1.706362323152461, 0.9504568842024205, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289369, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100872', 'abnormal neuroendocrine cell', 0.5, 6.2194654996189955, 1.763443435386998, 'UPHENO:0003116', 'abnormal endocrine system'),
(289370, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100515', 'abnormal somatic stem cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(289371, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100888', 'abnormal microtubule', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(289372, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100031', 'abnormal central nervous system', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(289373, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100295', 'abnormal extracellular matrix', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289374, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0131666', 'abnormal adherens junction', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(289375, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100842', 'abnormal left-dorsal blastomere', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(289376, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100745', 'abnormal anterior lymph sac', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(289377, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0141265', 'abnormal escape behavior', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(289378, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100989', 'abnormal right blastomere', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(289379, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0141748', 'abnormal gas homeostasis', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(289380, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0101149', 'abnormal amputated limb', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289381, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0101096', 'abnormal tendon', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(289382, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0101141', 'abnormal Keller explant', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289383, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0141264', 'abnormal schooling behavior', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(289384, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0126814', 'abnormally localised endocrine system', 0.43333333333333335, 6.2194654996189955, 1.6416764956901726, 'UPHENO:0003116', 'abnormal endocrine system'),
(289385, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100458', 'abnormal autopod', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(289386, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0141794', 'abnormal prosthetic group metabolic process', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(289387, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100006', 'abnormal anatomical structure', 0.5294117647058824, 1.706362323152461, 0.9504568842024205, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289388, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100014', 'abnormal tissue', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289389, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100378', 'abnormal perichondrium', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(289390, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100742', 'abnormal musculoskeletal system', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289391, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100796', 'abnormal pseudoblastema', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289392, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100416', 'abnormal ligament', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(289393, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0107271', 'abnormal apical region', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289394, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0101406', 'abnormal cleavage furrow', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289395, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100249', 'abnormal avascular GAG-rich matrix', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289396, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100907', 'abnormal cytoplasm', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(289397, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100069', 'abnormal urinary system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(289398, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100533', 'abnormal melanoblast', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(289399, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0102113', 'abnormal anatomical line morphology', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289400, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0107259', 'abnormal animal-vegetal axis', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289401, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0101378', 'abnormal blastomere D1', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(289402, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0101040', 'abnormal axial mesoderm', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289403, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100427', 'abnormal olfactory system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(289404, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0101221', 'abnormal larval immune system', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(289405, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100258', 'abnormal organ part', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289406, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100484', 'abnormal cement gland primordium', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289407, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100152', 'abnormal alimentary system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(289408, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0141777', 'abnormal catabolic process', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(289409, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100175', 'abnormal migrating neuroblast', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(289410, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0101202', 'abnormal thymus', 0.43333333333333335, 6.2194654996189955, 1.6416764956901726, 'UPHENO:0003116', 'abnormal endocrine system'),
(289411, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100823', 'abnormal blood', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(289412, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100894', 'abnormal nucleus', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(289413, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100172', 'abnormal stem cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(289414, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0141860', 'abnormal malate-aspartate shuttle', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(289415, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0101463', 'abnormal right-ventral blastomere', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(289416, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0107312', 'abnormal filopodium', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(289417, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100162', 'abnormal presumptive rhombomere', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289418, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100900', 'abnormal angioblast', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(289419, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100392', 'abnormal cilium', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(289420, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0101501', 'abnormal parabrachial area', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(289421, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100317', 'abnormal respiratory system', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(289422, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0101098', 'abnormal mineralized extracellular matrix', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289423, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100393', 'abnormal involuting marginal zone', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289424, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0101573', 'abnormal peripheral vegetal yolk mass', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289425, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100854', 'abnormal spiracle', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289426, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100756', 'abnormal adrenal medulla', 0.41935483870967744, 6.2194654996189955, 1.6149807898093176, 'UPHENO:0003116', 'abnormal endocrine system'),
(289427, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0141775', 'abnormal nitrogen compound metabolic process', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(289428, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0101109', 'abnormal egg cell-free extract', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289429, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0141778', 'abnormal biosynthetic process', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(289430, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100225', 'abnormal endocrine system', 0.6190476190476191, 6.2194654996189955, 1.9621787149207255, 'UPHENO:0003116', 'abnormal endocrine system'),
(289431, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0107273', 'abnormal basal region', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289432, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0141743', 'abnormal chemical homeostasis within a tissue', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(289433, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100423', 'abnormal process', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289434, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100273', 'abnormal visual system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(289435, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0101212', 'abnormal glomeral mesenchyme', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(289436, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0115391', 'abnormally undifferentiated alimentary system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(289437, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100207', 'abnormal blastema', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289438, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0101107', 'abnormal erythroid cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(289439, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100004', 'abnormal cell', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(289440, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100800', 'abnormal ventral marginal zone', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289441, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0101224', 'abnormal dorsal involuting marginal zone', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289442, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100308', 'abnormal early embryonic cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(289443, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0101302', 'abnormal subcortical cytoplasm', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(289444, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0141714', 'abnormal anterior notochord', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(289445, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100754', 'abnormal electrically active cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(289446, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0101467', 'abnormal alkali secreting cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(289447, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0141796', 'abnormal demethylation', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(289448, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100120', 'abnormal genital system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(289449, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0107253', 'abnormal enteric nervous system', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(289450, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100840', 'abnormal thyroid', 0.48148148148148145, 6.2194654996189955, 1.7304789691815143, 'UPHENO:0003116', 'abnormal endocrine system'),
(289451, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100158', 'abnormal neuromere', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(289452, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100081', 'abnormal anatomical entity in vitro', 0.5294117647058824, 1.706362323152461, 0.9504568842024205, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289453, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100493', 'abnormal liver and biliary system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(289454, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100588', 'abnormal unicellular gland', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289455, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100218', 'abnormal epithelial cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(289456, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100231', 'abnormal compound organ', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289457, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100003', 'abnormal organism subdivision', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289458, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0142051', 'abnormal cerebrospinal fluid', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(289459, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0101366', 'abnormal morula cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(289460, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100862', 'abnormal blastomere V1', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(289461, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100028', 'abnormal anatomical cluster', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289462, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0141841', 'abnormality of whole organism mass', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(289463, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100402', 'abnormal zeugopod', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(289464, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0131723', 'abnormal pathway-restricted SMAD protein phosphorylation', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(289465, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0116494', 'absent biological process', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(289466, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0141782', 'abnormal methylation', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(289467, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0101461', 'abnormal sperm entry point', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(289468, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0101092', 'abnormal dorso-lateral marginal zone', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289469, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100289', 'abnormal chondroblast', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(289470, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0101311', 'abnormal bottle cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(289471, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0115508', 'abnormally peramorphic growth of whole organism', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289472, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100551', 'abnormal oocyte cortex', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(289473, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100277', 'abnormal blastocoel', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289474, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0141792', 'abnormal small molecule metabolic process', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(289475, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100549', 'abnormal mitotic cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(289476, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0101074', 'abnormal germinal vesicle', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(289477, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100727', 'abnormal odontogenic papilla', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(289478, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0141787', 'abnormal hormone metabolic process', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(289479, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100935', 'abnormal skeleton', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(289480, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0101347', 'abnormal hindlimb region', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289481, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100531', 'abnormal proliferative region', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289482, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100599', 'abnormal adult immune system', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(289483, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0101297', 'abnormal barrier cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(289484, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100108', 'abnormal cell part', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(289485, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0101333', 'abnormal barrier epithelial cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(289486, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0116434', 'abnormal biological process', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(289487, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100151', 'abnormal primordium', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289488, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100274', 'abnormal sensory system', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(289489, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0101575', 'abnormal vitelline membrane', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(289490, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0115512', 'abnormally semi-erect whole organism', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289491, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100251', 'abnormal proteinaceous extracellular matrix', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289492, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0101553', 'abnormal dental epithelium', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289493, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0101326', 'abnormal cementoblast', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(289494, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100899', 'abnormal secondary spermatogonium', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(289495, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100265', 'abnormal sensory epithelial cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(289496, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100969', 'abnormal disaggregated/reaggregated ectoderm treated with activin', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289497, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0101240', 'abnormal ciliated non-epidermal cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(289498, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0107339', 'abnormal yolk platelet', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(289499, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0141797', 'abnormal hydrogen metabolic process', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(289500, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100293', 'abnormal duct', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289501, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100444', 'abnormal cement gland', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289502, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100724', 'abnormal kinetochore', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(289503, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100640', 'abnormal notochordal sheath', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(289504, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100372', 'abnormal hematological system', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(289505, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0101498', 'abnormal stage II oocyte', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(289506, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0101200', 'abnormal joint region', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289507, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0101480', 'abnormal stage V oocyte', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(289508, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100846', 'abnormal hindlimb', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(289509, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0141784', 'abnormal cellular hormone metabolic process', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(289510, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100394', 'abnormal marginal zone', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289511, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0101638', 'abnormal anatomical structure morphology', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289512, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100232', 'abnormal lymphatic system', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(289513, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0141276', 'decreased surface breathing', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(289514, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0101411', 'abnormal marginal zone (sensu neural)', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289515, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100674', 'abnormal secondary oogonium', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(289516, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100176', 'abnormal stage VI oocyte', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(289517, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0107258', 'abnormal anatomical axis', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289518, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0101513', 'abnormal basal body', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(289519, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100912', 'abnormal trabecula', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289520, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0101168', 'abnormal circulating cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(289521, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0101472', 'abnormal zygote cortex', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(289522, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100188', 'abnormal delta cell', 0.40625, 6.2194654996189955, 1.5895464319170476, 'UPHENO:0003116', 'abnormal endocrine system'),
(289523, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100587', 'abnormal vestibuloauditory system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(289524, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0142052', 'abnormal nasal region', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(289525, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0131667', 'abnormal actin cytoskeleton', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(289526, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100403', 'abnormal forelimb', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(289527, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0101264', 'abnormal mitotic spindle', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(289528, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100104', 'abnormal embryonic structure', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289529, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100465', 'abnormal skeletal system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(289530, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100026', 'abnormal germ cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(289531, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0131675', 'abnormal spindle microtubule', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(289532, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0115509', 'abnormally semi-viable whole organism', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289533, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0107266', 'abnormal dorsal side', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289534, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100610', 'abnormal appendage', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289535, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100135', 'abnormal surface structure', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289536, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100553', 'abnormal laryngeal muscle primordium', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289537, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0101450', 'abnormal myeloid cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(289538, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100062', 'abnormal anatomical space', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289539, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0101349', 'abnormal trunk region', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289540, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100702', 'abnormal glial cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(289541, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0107272', 'abnormal axial region', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289542, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100791', 'abnormal multiciliated cell precursor', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(289543, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100781', 'abnormal presumptive ectoderm', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289544, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100511', 'abnormal stylopod', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(289545, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100547', 'abnormal blastomere V2', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(289546, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0101451', 'abnormal dorsal lymph space', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(289547, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0101241', 'abnormal nucleate erythrocyte', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(289548, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100665', 'abnormal egg jelly', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289549, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0141791', 'abnormal primary metabolic process', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(289550, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100268', 'abnormal circulatory system', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289551, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0101157', 'abnormal female organism', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289552, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100060', 'abnormal regenerating tissue', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289553, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100722', 'abnormal barbel', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289554, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100704', 'abnormal Merkel cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(289555, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100557', 'abnormal prime meridian', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289556, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100581', 'abnormal immune system', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(289557, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100070', 'abnormal anatomical system', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289558, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0101283', 'abnormal left-ventral blastomere', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(289559, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0101078', 'abnormal mucous gland', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289560, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0125191', 'absent endocrine system', 0.40625, 6.2194654996189955, 1.5895464319170476, 'UPHENO:0003116', 'abnormal endocrine system'),
(289561, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100205', 'abnormal limb segment', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(289562, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0107284', 'abnormal migrating myoblast', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(289563, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100103', 'abnormal trunk', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289564, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100913', 'abnormal Brachets cleft', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289565, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100202', 'abnormal embryo', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289566, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100574', 'abnormal gastrula cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(289567, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100383', 'abnormal amputated fin', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289568, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0101468', 'abnormal stage I oocyte', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(289569, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100282', 'abnormal pelvic girdle primordium', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289570, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0101071', 'abnormal endoplasmic reticulum', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(289571, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100482', 'abnormal Mullerian duct', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(289572, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0141263', 'abnormal visually guided collision avoidance behavior', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(289573, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0101587', 'abnormal hemangioblast', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(289574, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100545', 'abnormal male organism', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289575, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0101570', 'abnormal forelimb region', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289576, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0141772', 'abnormal water homeostasis', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(289577, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0100627', 'abnormal pharyngeal region', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(289578, 'HP:0002929', 'Leydig cell insensitivity to gonadotropin', 'XPO:0107278', 'abnormal medial region', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289579, 'HP:0009882', 'Short distal phalanx of finger', 'XPO:0103634', 'abnormally increased number of forelimb digit', 0.41304347826086957, 7.774297771301195, 1.7919606559559202, 'HP:0005918', 'Abnormal finger phalanx morphology'),
(289580, 'HP:0009882', 'Short distal phalanx of finger', 'XPO:0103822', 'decreased length of forelimb digit 3 in regenerating forelimb', 0.46853146853146854, 12.379159829460056, 2.408324300023293, 'UPHENO:0046707', 'decreased length of manual digit'),
(289581, 'HP:0009882', 'Short distal phalanx of finger', 'XPO:0125257', 'absent forelimb digit', 0.40145985401459855, 11.103525386846629, 2.1113075760890068, 'HP:0006265', 'Aplasia/Hypoplasia of fingers'),
(289582, 'HP:0009882', 'Short distal phalanx of finger', 'XPO:0103823', 'decreased length of forelimb digit 4 in regenerating forelimb', 0.46853146853146854, 12.379159829460056, 2.408324300023293, 'UPHENO:0046707', 'decreased length of manual digit'),
(289583, 'HP:0009882', 'Short distal phalanx of finger', 'XPO:0103821', 'decreased length of forelimb digit 2 in regenerating forelimb', 0.46853146853146854, 12.379159829460056, 2.408324300023293, 'UPHENO:0046707', 'decreased length of manual digit'),
(289584, 'HP:0009882', 'Short distal phalanx of finger', 'XPO:0103824', 'decreased length of forelimb digit 5 in regenerating forelimb', 0.46853146853146854, 12.379159829460056, 2.408324300023293, 'UPHENO:0046707', 'decreased length of manual digit'),
(289585, 'HP:0000055', 'Abnormal female external genitalia morphology', 'XPO:0102844', 'abnormal glomeral mesenchyme morphology', 0.425, 5.4478002382576385, 1.5216159506457259, 'HP:0000119', 'Abnormality of the genitourinary system'),
(289586, 'HP:0000055', 'Abnormal female external genitalia morphology', 'XPO:0102864', 'abnormal female genitalia morphology', 0.5714285714285714, 7.960567433004586, 2.1328140275238767, 'UPHENO:0005170', 'abnormal female reproductive system'),
(289587, 'HP:0000055', 'Abnormal female external genitalia morphology', 'XPO:0100414', 'abnormal testis', 0.4583333333333333, 7.005035523447265, 1.7918262420167856, 'UPHENO:0020950', 'abnormal reproductive system morphology'),
(289588, 'HP:0000055', 'Abnormal female external genitalia morphology', 'XPO:0102178', 'abnormal whole organism morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(289589, 'HP:0000055', 'Abnormal female external genitalia morphology', 'XPO:0103201', 'abnormal activin-induced ectoderm morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(289590, 'HP:0000055', 'Abnormal female external genitalia morphology', 'XPO:0139866', 'abnormally necrotic male genitalia', 0.44, 7.005035523447265, 1.755624000267938, 'HP:0012243', 'Abnormal reproductive system morphology'),
(289591, 'HP:0000055', 'Abnormal female external genitalia morphology', 'XPO:0129028', 'decreased size of the male genitalia', 0.4230769230769231, 7.005035523447265, 1.7215309684419309, 'HP:0012243', 'Abnormal reproductive system morphology'),
(289592, 'HP:0000055', 'Abnormal female external genitalia morphology', 'XPO:0129864', 'increased size of the genital system', 0.4888888888888889, 7.005035523447265, 1.8505901852342483, 'UPHENO:0020950', 'abnormal reproductive system morphology'),
(289593, 'HP:0000055', 'Abnormal female external genitalia morphology', 'XPO:0140839', 'abnormally necrotic female genitalia', 0.5, 7.960567433004586, 1.9950648401749487, 'UPHENO:0005170', 'abnormal female reproductive system'),
(289594, 'HP:0000055', 'Abnormal female external genitalia morphology', 'XPO:0141640', 'neoplastic gonad', 0.4166666666666667, 6.723205497167461, 1.6737190994368725, 'UPHENO:0087547', 'abnormal reproductive system morphology'),
(289595, 'HP:0000055', 'Abnormal female external genitalia morphology', 'XPO:0101669', 'abnormal gonad morphology', 0.4444444444444444, 6.723205497167461, 1.7286096528928754, 'UPHENO:0087547', 'abnormal reproductive system morphology'),
(289596, 'HP:0000055', 'Abnormal female external genitalia morphology', 'XPO:0128383', 'decreased size of the female genitalia', 0.48, 7.960567433004586, 1.9547563448783587, 'UPHENO:0005170', 'abnormal female reproductive system'),
(289597, 'HP:0000055', 'Abnormal female external genitalia morphology', 'XPO:0103125', 'abnormal fat body morphology', 0.4166666666666667, 6.723205497167461, 1.6737190994368725, 'UPHENO:0087547', 'abnormal reproductive system morphology'),
(289598, 'HP:0000055', 'Abnormal female external genitalia morphology', 'XPO:0125335', 'absent female genitalia', 0.5217391304347826, 7.960567433004586, 2.037974369383301, 'UPHENO:0005170', 'abnormal female reproductive system'),
(289599, 'HP:0000055', 'Abnormal female external genitalia morphology', 'XPO:0100036', 'abnormal ovary', 0.4444444444444444, 7.960567433004586, 1.8809651698594156, 'UPHENO:0005170', 'abnormal female reproductive system'),
(289600, 'HP:0000055', 'Abnormal female external genitalia morphology', 'XPO:0102270', 'abnormal polar body morphology', 0.5116279069767442, 7.005035523447265, 1.8931380465140588, 'UPHENO:0020950', 'abnormal reproductive system morphology'),
(289601, 'HP:0000055', 'Abnormal female external genitalia morphology', 'XPO:0101638', 'abnormal anatomical structure morphology', 0.43333333333333335, 2.786899518863159, 1.0989342374200721, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(289602, 'HP:0000055', 'Abnormal female external genitalia morphology', 'XPO:0102113', 'abnormal anatomical line morphology', 0.43333333333333335, 2.786899518863159, 1.0989342374200721, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(289603, 'HP:0000055', 'Abnormal female external genitalia morphology', 'XPO:0102742', 'abnormal cell-free extract morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(289604, 'HP:0000055', 'Abnormal female external genitalia morphology', 'XPO:0141316', 'abnormal anatomical region morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(289605, 'HP:0000055', 'Abnormal female external genitalia morphology', 'XPO:0100964', 'abnormal follicle layer', 0.42857142857142855, 7.960567433004586, 1.8470711293834803, 'UPHENO:0005170', 'abnormal female reproductive system'),
(289606, 'HP:0000055', 'Abnormal female external genitalia morphology', 'XPO:0101752', 'abnormal genital system morphology', 0.5789473684210527, 7.005035523447265, 2.0138388421112015, 'HP:0012243', 'Abnormal reproductive system morphology'),
(289607, 'HP:0000055', 'Abnormal female external genitalia morphology', 'XPO:0141148', 'abnormally necrotic oviduct', 0.46153846153846156, 7.960567433004586, 1.9167962974719344, 'UPHENO:0005170', 'abnormal female reproductive system'),
(289608, 'HP:0000055', 'Abnormal female external genitalia morphology', 'XPO:0102397', 'abnormal male genitalia morphology', 0.5, 7.005035523447265, 1.8715014725411339, 'HP:0012243', 'Abnormal reproductive system morphology'),
(289609, 'HP:0000055', 'Abnormal female external genitalia morphology', 'XPO:0140269', 'abnormally necrotic anatomical line', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(289610, 'HP:0000055', 'Abnormal female external genitalia morphology', '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'),
(289611, 'HP:0000055', 'Abnormal female external genitalia morphology', 'XPO:0139858', 'abnormally necrotic urogenital system', 0.40476190476190477, 5.4478002382576385, 1.4849451172348156, 'HP:0000119', 'Abnormality of the genitourinary system'),
(289612, 'HP:0000055', 'Abnormal female external genitalia morphology', 'XPO:0101948', 'abnormal gamete morphology', 0.4444444444444444, 6.723205497167461, 1.7286096528928754, 'UPHENO:0087547', 'abnormal reproductive system morphology'),
(289613, 'HP:0000055', 'Abnormal female external genitalia morphology', 'XPO:0127432', 'abnormally localised oviduct', 0.4897959183673469, 7.960567433004586, 1.974602095758453, 'UPHENO:0005170', 'abnormal female reproductive system'),
(289614, 'HP:0000055', 'Abnormal female external genitalia morphology', 'XPO:0101740', 'abnormal cell part morphology', 0.4166666666666667, 2.786899518863159, 1.0775936770692605, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(289615, 'HP:0000055', 'Abnormal female external genitalia morphology', 'XPO:0139718', 'abnormally necrotic anatomical structure', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(289616, 'HP:0000055', 'Abnormal female external genitalia morphology', 'XPO:0125139', 'absent male genitalia', 0.4583333333333333, 7.005035523447265, 1.7918262420167856, 'HP:0012243', 'Abnormal reproductive system morphology'),
(289617, 'HP:0000055', 'Abnormal female external genitalia morphology', 'XPO:0100628', 'abnormal primary oogonium', 0.4067796610169492, 7.960567433004586, 1.7994990752707185, 'UPHENO:0005170', 'abnormal female reproductive system'),
(289618, 'HP:0000055', 'Abnormal female external genitalia morphology', 'XPO:0101232', 'abnormal female genitalia', 0.6666666666666666, 7.960567433004586, 2.3037024450515284, 'UPHENO:0005170', 'abnormal female reproductive system'),
(289619, 'HP:0000055', 'Abnormal female external genitalia morphology', 'XPO:0140144', 'abnormally necrotic portion of organism substance', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(289620, 'HP:0000055', 'Abnormal female external genitalia morphology', 'XPO:0126762', 'abnormally localised male genitalia', 0.46808510638297873, 7.005035523447265, 1.810787894318205, 'HP:0012243', 'Abnormal reproductive system morphology'),
(289621, 'HP:0000055', 'Abnormal female external genitalia morphology', 'XPO:0129863', 'increased size of the female genitalia', 0.48, 7.960567433004586, 1.9547563448783587, 'UPHENO:0005170', 'abnormal female reproductive system'),
(289622, 'HP:0000055', 'Abnormal female external genitalia morphology', 'XPO:0100278', 'abnormal follicle cell', 0.41379310344827586, 7.960567433004586, 1.8149457025796234, 'UPHENO:0005170', 'abnormal female reproductive system'),
(289623, 'HP:0000055', 'Abnormal female external genitalia morphology', 'XPO:0100120', 'abnormal genital system', 0.4411764705882353, 6.57633172329375, 1.7033269853730915, 'UPHENO:0003055', 'abnormal reproductive system'),
(289624, 'HP:0000055', 'Abnormal female external genitalia morphology', 'XPO:0101701', 'abnormal urinary system morphology', 0.4146341463414634, 5.4478002382576385, 1.5029451091868848, 'HP:0000119', 'Abnormality of the genitourinary system'),
(289625, 'HP:0000055', 'Abnormal female external genitalia morphology', 'XPO:0102894', 'abnormal oviduct morphology', 0.5217391304347826, 7.960567433004586, 2.037974369383301, 'UPHENO:0005170', 'abnormal female reproductive system'),
(289626, 'HP:0000055', 'Abnormal female external genitalia morphology', 'XPO:0102556', 'abnormal spermatozoon morphology', 0.425531914893617, 6.723205497167461, 1.6914309058997834, 'UPHENO:0087547', 'abnormal reproductive system morphology'),
(289627, 'HP:0000055', 'Abnormal female external genitalia morphology', 'XPO:0107345', 'abnormal anatomical axis morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(289628, 'HP:0000055', 'Abnormal female external genitalia morphology', 'XPO:0102133', 'abnormal urogenital system morphology', 0.4594594594594595, 5.4478002382576385, 1.582100930001929, 'HP:0000119', 'Abnormality of the genitourinary system'),
(289629, 'HP:0000055', 'Abnormal female external genitalia morphology', 'XPO:0140723', 'abnormally necrotic polar body', 0.46808510638297873, 7.005035523447265, 1.810787894318205, 'UPHENO:0020950', 'abnormal reproductive system morphology'),
(289630, 'HP:0000055', 'Abnormal female external genitalia morphology', 'XPO:0128607', 'decreased size of the oviduct', 0.4444444444444444, 7.960567433004586, 1.8809651698594156, 'UPHENO:0005170', 'abnormal female reproductive system'),
(289631, 'HP:0000055', 'Abnormal female external genitalia morphology', 'XPO:0101262', 'abnormal oviduct', 0.6, 7.960567433004586, 2.1854840332985166, 'UPHENO:0005170', 'abnormal female reproductive system'),
(289632, 'HP:0000055', 'Abnormal female external genitalia morphology', 'XPO:0101890', 'abnormal organ part morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(289633, 'HP:0000055', 'Abnormal female external genitalia morphology', 'XPO:0101976', 'abnormal portion of organism substance morphology', 0.43333333333333335, 2.786899518863159, 1.0989342374200721, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(289634, 'HP:0000055', 'Abnormal female external genitalia morphology', 'XPO:0125782', 'absent oviduct', 0.47058823529411764, 7.960567433004586, 1.9354971919993715, 'UPHENO:0005170', 'abnormal female reproductive system'),
(289635, 'HP:0000055', 'Abnormal female external genitalia morphology', 'XPO:0101372', 'abnormal seminiferous tubule', 0.43137254901960786, 7.005035523447265, 1.7383267902561792, 'HP:0012243', 'Abnormal reproductive system morphology'),
(289636, 'HP:0000055', 'Abnormal female external genitalia morphology', 'XPO:0101636', 'abnormal cell morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(289637, 'HP:0000055', 'Abnormal female external genitalia morphology', 'XPO:0139867', 'abnormally necrotic genital system', 0.5116279069767442, 7.005035523447265, 1.8931380465140588, 'HP:0012243', 'Abnormal reproductive system morphology'),
(289638, 'HP:0000055', 'Abnormal female external genitalia morphology', 'XPO:0126964', 'abnormally localised female genitalia', 0.5333333333333333, 7.960567433004586, 2.060494106827077, 'UPHENO:0005170', 'abnormal female reproductive system'),
(289639, 'HP:0000055', 'Abnormal female external genitalia morphology', 'XPO:0100765', 'abnormal male genitalia', 0.5789473684210527, 7.005035523447265, 2.0138388421112015, 'UPHENO:0020950', 'abnormal reproductive system morphology'),
(289640, 'HP:0000055', 'Abnormal female external genitalia morphology', 'XPO:0102773', 'abnormal Keller explant morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(289641, 'HP:0000055', 'Abnormal female external genitalia morphology', 'XPO:0100666', 'abnormal primary spermatogonium', 0.41509433962264153, 7.005035523447265, 1.705212771075354, 'HP:0012243', 'Abnormal reproductive system morphology'),
(289642, 'HP:0000055', 'Abnormal female external genitalia morphology', 'XPO:0101694', 'abnormal anatomical space morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(289643, 'HP:0000055', 'Abnormal female external genitalia morphology', 'XPO:0130505', 'increased size of the male genitalia', 0.4230769230769231, 7.005035523447265, 1.7215309684419309, 'HP:0012243', 'Abnormal reproductive system morphology'),
(289644, 'HP:0000055', 'Abnormal female external genitalia morphology', 'XPO:0128384', 'decreased size of the genital system', 0.4888888888888889, 7.005035523447265, 1.8505901852342483, 'HP:0012243', 'Abnormal reproductive system morphology'),
(289645, 'HP:0000055', 'Abnormal female external genitalia morphology', 'XPO:0130087', 'increased size of the oviduct', 0.4444444444444444, 7.960567433004586, 1.8809651698594156, 'UPHENO:0005170', 'abnormal female reproductive system'),
(289646, 'HP:0000055', 'Abnormal female external genitalia morphology', 'XPO:0101713', 'abnormal anatomical entity in vitro morphology', 0.43333333333333335, 2.786899518863159, 1.0989342374200721, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(289647, 'HP:0000055', 'Abnormal female external genitalia morphology', 'XPO:0102648', 'abnormal egg morphology', 0.425531914893617, 6.723205497167461, 1.6914309058997834, 'UPHENO:0087547', 'abnormal reproductive system morphology'),
(289648, 'HP:3000076', 'Abnormality of lingual tonsil', 'XPO:0127194', 'abnormally localised aortic arch 2', 0.449438202247191, 8.127241455820435, 1.9112019226478347, 'HP:0000600', 'Abnormality of the pharynx'),
(289649, 'HP:3000076', 'Abnormality of lingual tonsil', 'XPO:0125250', 'absent aortic arch 5', 0.43478260869565216, 8.127241455820435, 1.8797827644866465, 'HP:0000600', 'Abnormality of the pharynx'),
(289650, 'HP:3000076', 'Abnormality of lingual tonsil', 'XPO:0101036', 'abnormal pharynx', 0.4383561643835616, 8.127241455820435, 1.8874920904715122, 'HP:0000600', 'Abnormality of the pharynx'),
(289651, 'HP:3000076', 'Abnormality of lingual tonsil', 'XPO:0141145', 'abnormally necrotic aortic arch 5', 0.4036697247706422, 8.127241455820435, 1.8112761582971242, 'HP:0000600', 'Abnormality of the pharynx'),
(289652, 'HP:3000076', 'Abnormality of lingual tonsil', 'XPO:0101992', 'abnormal aortic arch 6 morphology', 0.43137254901960786, 8.127241455820435, 1.8723965560999865, 'HP:0000600', 'Abnormality of the pharynx'),
(289653, 'HP:3000076', 'Abnormality of lingual tonsil', 'XPO:0125070', 'absent aortic arch 6', 0.43010752688172044, 8.127241455820435, 1.8696490908546237, 'HP:0000600', 'Abnormality of the pharynx'),
(289654, 'HP:3000076', 'Abnormality of lingual tonsil', 'XPO:0103106', 'abnormal aortic arch 5 morphology', 0.44, 8.127241455820435, 1.8910278264903961, 'HP:0000600', 'Abnormality of the pharynx'),
(289655, 'HP:3000076', 'Abnormality of lingual tonsil', 'XPO:0102668', 'abnormal pharynx morphology', 0.43037974683544306, 8.127241455820435, 1.870240658371675, 'HP:0000600', 'Abnormality of the pharynx'),
(289656, 'HP:3000076', 'Abnormality of lingual tonsil', 'XPO:0103199', 'abnormal tongue morphology', 0.4805194805194805, 10.93592543835056, 2.2923623646003226, 'HP:0000157', 'Abnormality of the tongue'),
(289657, 'HP:3000076', 'Abnormality of lingual tonsil', 'XPO:0125536', 'absent aortic arch 1', 0.43478260869565216, 8.127241455820435, 1.8797827644866465, 'HP:0000600', 'Abnormality of the pharynx'),
(289658, 'HP:3000076', 'Abnormality of lingual tonsil', 'XPO:0129585', 'increased size of the tongue', 0.40425531914893614, 11.945263302929897, 2.197484067938605, 'HP:0030809', 'Abnormal tongue morphology'),
(289659, 'HP:3000076', 'Abnormality of lingual tonsil', 'XPO:0126876', 'abnormally localised aortic arch', 0.45977011494252873, 8.127241455820435, 1.933044939546995, 'HP:0000600', 'Abnormality of the pharynx'),
(289660, 'HP:3000076', 'Abnormality of lingual tonsil', 'XPO:0128105', 'decreased size of the tongue', 0.42696629213483145, 11.945263302929897, 2.2583677249345926, 'HP:0030809', 'Abnormal tongue morphology'),
(289661, 'HP:3000076', 'Abnormality of lingual tonsil', 'XPO:0101474', 'abnormal aortic arch 5', 0.5194805194805194, 8.127241455820435, 2.0547368720625063, 'HP:0000600', 'Abnormality of the pharynx'),
(289662, 'HP:3000076', 'Abnormality of lingual tonsil', 'XPO:0125328', 'absent aortic arch 4', 0.43010752688172044, 8.127241455820435, 1.8696490908546237, 'HP:0000600', 'Abnormality of the pharynx'),
(289663, 'HP:3000076', 'Abnormality of lingual tonsil', 'XPO:0140110', 'abnormally necrotic pharynx', 0.40476190476190477, 8.127241455820435, 1.81372482260066, 'HP:0000600', 'Abnormality of the pharynx'),
(289664, 'HP:3000076', 'Abnormality of lingual tonsil', 'XPO:0128496', 'decreased size of the aortic arch', 0.4074074074074074, 8.127241455820435, 1.8196423744488384, 'HP:0000600', 'Abnormality of the pharynx'),
(289665, 'HP:3000076', 'Abnormality of lingual tonsil', 'XPO:0101894', 'abnormal aortic arch 4 morphology', 0.43137254901960786, 8.127241455820435, 1.8723965560999865, 'HP:0000600', 'Abnormality of the pharynx'),
(289666, 'HP:3000076', 'Abnormality of lingual tonsil', 'XPO:0141311', 'abnormal roof of mouth morphology', 0.4024390243902439, 7.312692920701687, 1.7154920590526295, 'UPHENO:0076800', 'abnormal mouth morphology'),
(289667, 'HP:3000076', 'Abnormality of lingual tonsil', 'XPO:0129976', 'increased size of the aortic arch', 0.4074074074074074, 8.127241455820435, 1.8196423744488384, 'HP:0000600', 'Abnormality of the pharynx'),
(289668, 'HP:3000076', 'Abnormality of lingual tonsil', 'XPO:0101567', 'abnormal tongue', 0.4788732394366197, 10.93592543835056, 2.2884322233573506, 'HP:0000157', 'Abnormality of the tongue'),
(289669, 'HP:3000076', 'Abnormality of lingual tonsil', 'XPO:0126957', 'abnormally localised aortic arch 4', 0.449438202247191, 8.127241455820435, 1.9112019226478347, 'HP:0000600', 'Abnormality of the pharynx'),
(289670, 'HP:3000076', 'Abnormality of lingual tonsil', 'XPO:0127174', 'abnormally localised aortic arch 1', 0.449438202247191, 8.127241455820435, 1.9112019226478347, 'HP:0000600', 'Abnormality of the pharynx'),
(289671, 'HP:3000076', 'Abnormality of lingual tonsil', 'XPO:0125387', 'absent aortic arch 3', 0.43010752688172044, 8.127241455820435, 1.8696490908546237, 'HP:0000600', 'Abnormality of the pharynx'),
(289672, 'HP:3000076', 'Abnormality of lingual tonsil', 'XPO:0100262', 'abnormal aortic arch 4', 0.5194805194805194, 8.127241455820435, 2.0547368720625063, 'HP:0000600', 'Abnormality of the pharynx'),
(289673, 'HP:3000076', 'Abnormality of lingual tonsil', 'XPO:0103096', 'abnormal oral cavity morphology', 0.4430379746835443, 7.884497199543557, 1.8689921537245293, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(289674, 'HP:3000076', 'Abnormality of lingual tonsil', 'XPO:0129152', 'decreased size of the oral cavity', 0.4166666666666667, 7.884497199543557, 1.812514045870123, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(289675, 'HP:3000076', 'Abnormality of lingual tonsil', 'XPO:0140626', 'abnormally necrotic tongue', 0.45121951219512196, 10.93592543835056, 2.221374111151646, 'HP:0000157', 'Abnormality of the tongue'),
(289676, 'HP:3000076', 'Abnormality of lingual tonsil', 'XPO:0126690', 'abnormally localised aortic arch 6', 0.449438202247191, 8.127241455820435, 1.9112019226478347, 'HP:0000600', 'Abnormality of the pharynx'),
(289677, 'HP:3000076', 'Abnormality of lingual tonsil', 'XPO:0127750', 'abnormally localised tongue', 0.43209876543209874, 10.93592543835056, 2.173798491297839, 'HP:0000157', 'Abnormality of the tongue'),
(289678, 'HP:3000076', 'Abnormality of lingual tonsil', 'XPO:0102348', 'abnormal aortic arch 3 morphology', 0.43137254901960786, 8.127241455820435, 1.8723965560999865, 'HP:0000600', 'Abnormality of the pharynx'),
(289679, 'HP:3000076', 'Abnormality of lingual tonsil', 'XPO:0102279', 'abnormal mouth morphology', 0.4177215189873418, 7.312692920701687, 1.7477611949930372, 'UPHENO:0076800', 'abnormal mouth morphology'),
(289680, 'HP:3000076', 'Abnormality of lingual tonsil', 'XPO:0115393', 'abnormally decreased volume of oral cavity', 0.4069767441860465, 7.884497199543557, 1.791314321891677, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(289681, 'HP:3000076', 'Abnormality of lingual tonsil', 'XPO:0100116', 'abnormal aortic arch 1', 0.5194805194805194, 8.127241455820435, 2.0547368720625063, 'HP:0000600', 'Abnormality of the pharynx'),
(289682, 'HP:3000076', 'Abnormality of lingual tonsil', 'XPO:0140279', 'abnormally necrotic aortic arch', 0.41509433962264153, 8.127241455820435, 1.8367285931943074, 'HP:0000600', 'Abnormality of the pharynx'),
(289683, 'HP:3000076', 'Abnormality of lingual tonsil', 'XPO:0100716', 'abnormal aortic arch 3', 0.5194805194805194, 8.127241455820435, 2.0547368720625063, 'HP:0000600', 'Abnormality of the pharynx'),
(289684, 'HP:3000076', 'Abnormality of lingual tonsil', 'XPO:0101749', 'abnormal aortic arch morphology', 0.4489795918367347, 8.127241455820435, 1.91022657074831, 'HP:0000600', 'Abnormality of the pharynx'),
(289685, 'HP:3000076', 'Abnormality of lingual tonsil', 'XPO:0101210', 'abnormal aortic arch 2', 0.5194805194805194, 8.127241455820435, 2.0547368720625063, 'HP:0000600', 'Abnormality of the pharynx'),
(289686, 'HP:3000076', 'Abnormality of lingual tonsil', 'XPO:0101395', 'abnormal m. geniohyoideus', 0.41304347826086957, 8.127241455820435, 1.8321856018367806, 'HP:0000600', 'Abnormality of the pharynx'),
(289687, 'HP:3000076', 'Abnormality of lingual tonsil', 'XPO:0101748', 'abnormal aortic arch 1 morphology', 0.43137254901960786, 8.127241455820435, 1.8723965560999865, 'HP:0000600', 'Abnormality of the pharynx'),
(289688, 'HP:3000076', 'Abnormality of lingual tonsil', 'XPO:0130628', 'increased size of the oral cavity', 0.4166666666666667, 7.884497199543557, 1.812514045870123, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(289689, 'HP:3000076', 'Abnormality of lingual tonsil', 'XPO:0125251', 'absent aortic arch', 0.4444444444444444, 8.127241455820435, 1.900554475330284, 'HP:0000600', 'Abnormality of the pharynx'),
(289690, 'HP:3000076', 'Abnormality of lingual tonsil', 'XPO:0100586', 'abnormal thyroid primordium', 0.4155844155844156, 8.127241455820435, 1.8378125287228213, 'HP:0000600', 'Abnormality of the pharynx'),
(289691, 'HP:3000076', 'Abnormality of lingual tonsil', 'XPO:0100875', 'abnormal oropharynx', 0.42105263157894735, 8.127241455820435, 1.8498638875470566, 'HP:0000600', 'Abnormality of the pharynx'),
(289692, 'HP:3000076', 'Abnormality of lingual tonsil', 'XPO:0115558', 'abnormally incomplete structure of mouth', 0.4125, 7.312692920701687, 1.7368033365322182, 'UPHENO:0076800', 'abnormal mouth morphology'),
(289693, 'HP:3000076', 'Abnormality of lingual tonsil', 'XPO:0127022', 'abnormally localised aortic arch 3', 0.449438202247191, 8.127241455820435, 1.9112019226478347, 'HP:0000600', 'Abnormality of the pharynx'),
(289694, 'HP:3000076', 'Abnormality of lingual tonsil', 'XPO:0101329', 'abnormal pharyngeal epithelium', 0.43243243243243246, 8.127241455820435, 1.8746953863777802, 'HP:0000600', 'Abnormality of the pharynx'),
(289695, 'HP:3000076', 'Abnormality of lingual tonsil', 'XPO:0100117', 'abnormal aortic arch', 0.5263157894736842, 8.127241455820435, 2.068210700838623, 'HP:0000600', 'Abnormality of the pharynx'),
(289696, 'HP:3000076', 'Abnormality of lingual tonsil', 'XPO:0102842', 'abnormal aortic arch 2 morphology', 0.43137254901960786, 8.127241455820435, 1.8723965560999865, 'HP:0000600', 'Abnormality of the pharynx'),
(289697, 'HP:3000076', 'Abnormality of lingual tonsil', 'XPO:0100360', 'abnormal aortic arch 6', 0.5194805194805194, 8.127241455820435, 2.0547368720625063, 'HP:0000600', 'Abnormality of the pharynx'),
(289698, 'HP:3000076', 'Abnormality of lingual tonsil', 'XPO:0126089', 'absent tongue', 0.42168674698795183, 10.93592543835056, 2.1474484448761135, 'HP:0000157', 'Abnormality of the tongue'),
(289699, 'HP:3000076', 'Abnormality of lingual tonsil', 'XPO:0125557', 'absent aortic arch 2', 0.43010752688172044, 8.127241455820435, 1.8696490908546237, 'HP:0000600', 'Abnormality of the pharynx'),
(289700, 'HP:3000076', 'Abnormality of lingual tonsil', 'XPO:0126875', 'abnormally localised aortic arch 5', 0.449438202247191, 8.127241455820435, 1.9112019226478347, 'HP:0000600', 'Abnormality of the pharynx'),
(289701, 'HP:0100612', 'Odontogenic neoplasm', 'XPO:0128105', 'decreased size of the tongue', 0.4444444444444444, 7.884497199543557, 1.8719564571792031, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(289702, 'HP:0100612', 'Odontogenic neoplasm', 'XPO:0129990', 'increased size of the cementum', 0.40217391304347827, 9.181382707377857, 1.9215911663451926, 'UPHENO:0002826', 'abnormal dentition'),
(289703, 'HP:0100612', 'Odontogenic neoplasm', 'XPO:0131573', 'decreased size of the roof of mouth', 0.43478260869565216, 7.312692920701687, 1.7830961007901136, 'UPHENO:0076800', 'abnormal mouth morphology'),
(289704, 'HP:0100612', 'Odontogenic neoplasm', 'XPO:0130358', 'increased size of the lower jaw', 0.4230769230769231, 7.312692920701687, 1.7589291117884391, 'UPHENO:0076800', 'abnormal mouth morphology'),
(289705, 'HP:0100612', 'Odontogenic neoplasm', 'XPO:0103828', 'decreased width of the mouth', 0.4383561643835616, 7.884497199543557, 1.859090624602482, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(289706, 'HP:0100612', 'Odontogenic neoplasm', 'XPO:0115558', 'abnormally incomplete structure of mouth', 0.5, 7.312692920701687, 1.9121575406725366, 'UPHENO:0076800', 'abnormal mouth morphology'),
(289707, 'HP:0100612', 'Odontogenic neoplasm', 'XPO:0130466', 'increased size of the tooth', 0.43529411764705883, 9.181382707377857, 1.999150290595484, 'UPHENO:0002826', 'abnormal dentition'),
(289708, 'HP:0100612', 'Odontogenic neoplasm', 'XPO:0115393', 'abnormally decreased volume of oral cavity', 0.48484848484848486, 7.884497199543557, 1.9551947527013303, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(289709, 'HP:0100612', 'Odontogenic neoplasm', 'XPO:0128510', 'decreased size of the cementum', 0.40217391304347827, 9.181382707377857, 1.9215911663451926, 'UPHENO:0002826', 'abnormal dentition'),
(289710, 'HP:0100612', 'Odontogenic neoplasm', 'XPO:0140789', 'abnormally necrotic roof of mouth', 0.44776119402985076, 7.312692920701687, 1.8095137782694621, 'UPHENO:0076800', 'abnormal mouth morphology'),
(289711, 'HP:0100612', 'Odontogenic neoplasm', 'XPO:0128989', 'decreased size of the tooth', 0.43529411764705883, 9.181382707377857, 1.999150290595484, 'UPHENO:0002826', 'abnormal dentition'),
(289712, 'HP:0100612', 'Odontogenic neoplasm', 'XPO:0139736', 'abnormally necrotic tooth', 0.4567901234567901, 9.181382707377857, 2.0479172201061178, 'UPHENO:0002826', 'abnormal dentition'),
(289713, 'HP:0100612', 'Odontogenic neoplasm', 'XPO:0128880', 'decreased size of the lower jaw', 0.4230769230769231, 7.312692920701687, 1.7589291117884391, 'UPHENO:0076800', 'abnormal mouth morphology'),
(289714, 'HP:0100612', 'Odontogenic neoplasm', 'XPO:0103735', 'increased size of the mouth', 0.47058823529411764, 7.884497199543557, 1.9262273031277009, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(289715, 'HP:0100612', 'Odontogenic neoplasm', 'XPO:0101506', 'abnormal upper jaw', 0.49056603773584906, 7.0866363731414825, 1.8645275880090284, 'HP:0000153', 'Abnormality of the mouth'),
(289716, 'HP:0100612', 'Odontogenic neoplasm', 'XPO:0101659', 'abnormal lower jaw morphology', 0.4647887323943662, 7.312692920701687, 1.8435990000545652, 'UPHENO:0076800', 'abnormal mouth morphology'),
(289717, 'HP:0100612', 'Odontogenic neoplasm', 'XPO:0126046', 'absent tooth', 0.43529411764705883, 9.181382707377857, 1.999150290595484, 'UPHENO:0002826', 'abnormal dentition'),
(289718, 'HP:0100612', 'Odontogenic neoplasm', 'XPO:0129225', 'decreased size of the upper jaw', 0.4125, 7.312692920701687, 1.7368033365322182, 'UPHENO:0076800', 'abnormal mouth morphology'),
(289719, 'HP:0100612', 'Odontogenic neoplasm', 'XPO:0131651', 'abnormal roof of mouth', 0.41818181818181815, 7.0866363731414825, 1.721482641014341, 'HP:0000153', 'Abnormality of the mouth'),
(289720, 'HP:0100612', 'Odontogenic neoplasm', 'XPO:0103096', 'abnormal oral cavity morphology', 0.5423728813559322, 7.884497199543557, 2.0679307203480533, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(289721, 'HP:0100612', 'Odontogenic neoplasm', 'XPO:0103352', 'decreased size of the mouth', 0.47058823529411764, 7.884497199543557, 1.9262273031277009, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(289722, 'HP:0100612', 'Odontogenic neoplasm', 'XPO:0131611', 'increased size of the roof of mouth', 0.43478260869565216, 7.312692920701687, 1.7830961007901136, 'UPHENO:0076800', 'abnormal mouth morphology'),
(289723, 'HP:0100612', 'Odontogenic neoplasm', 'XPO:0102223', 'abnormal pharyngeal arch morphology', 0.4067796610169492, 5.725717590856133, 1.5261407080237526, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(289724, 'HP:0100612', 'Odontogenic neoplasm', 'XPO:0127750', 'abnormally localised tongue', 0.5245901639344263, 7.884497199543557, 2.0337476929179488, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(289725, 'HP:0100612', 'Odontogenic neoplasm', 'XPO:0101816', 'abnormal tooth morphology', 0.5068493150684932, 9.181382707377857, 2.1572152272353757, 'UPHENO:0002826', 'abnormal dentition'),
(289726, 'HP:0100612', 'Odontogenic neoplasm', 'XPO:0102960', 'abnormal oral epithelium morphology', 0.4411764705882353, 7.312692920701687, 1.7961592505261732, 'UPHENO:0076800', 'abnormal mouth morphology'),
(289727, 'HP:0100612', 'Odontogenic neoplasm', 'XPO:0130701', 'increased size of the upper jaw', 0.4125, 7.312692920701687, 1.7368033365322182, 'UPHENO:0076800', 'abnormal mouth morphology'),
(289728, 'HP:0100612', 'Odontogenic neoplasm', 'XPO:0103138', 'abnormal upper jaw morphology', 0.4520547945205479, 7.312692920701687, 1.8181688303509294, 'UPHENO:0076800', 'abnormal mouth morphology'),
(289729, 'HP:0100612', 'Odontogenic neoplasm', 'XPO:0141830', 'increased width of mouth', 0.4383561643835616, 7.884497199543557, 1.859090624602482, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(289730, 'HP:0100612', 'Odontogenic neoplasm', 'XPO:0126089', 'absent tongue', 0.5079365079365079, 7.884497199543557, 2.0012056302067838, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(289731, 'HP:0100612', 'Odontogenic neoplasm', 'XPO:0100184', 'abnormal tooth', 0.4482758620689655, 7.0866363731414825, 1.7823490200685401, 'HP:0000153', 'Abnormality of the mouth'),
(289732, 'HP:0100612', 'Odontogenic neoplasm', 'XPO:0140897', 'abnormally necrotic lower jaw', 0.4342105263157895, 7.312692920701687, 1.7819226251113227, 'UPHENO:0076800', 'abnormal mouth morphology'),
(289733, 'HP:0100612', 'Odontogenic neoplasm', 'XPO:0102279', 'abnormal mouth morphology', 0.5084745762711864, 7.312692920701687, 1.9282941773119304, 'UPHENO:0076800', 'abnormal mouth morphology'),
(289734, 'HP:0100612', 'Odontogenic neoplasm', 'XPO:0101567', 'abnormal tongue', 0.64, 7.884497199543557, 2.2463477486150443, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(289735, 'HP:0100612', 'Odontogenic neoplasm', 'XPO:0140639', 'abnormally necrotic upper jaw', 0.4230769230769231, 7.312692920701687, 1.7589291117884391, 'UPHENO:0076800', 'abnormal mouth morphology'),
(289736, 'HP:0100612', 'Odontogenic neoplasm', 'XPO:0101328', 'abnormal oral epithelium', 0.40350877192982454, 7.0866363731414825, 1.6910115138695967, 'HP:0000153', 'Abnormality of the mouth'),
(289737, 'HP:0100612', 'Odontogenic neoplasm', 'XPO:0102861', 'abnormal cementum morphology', 0.45121951219512196, 9.181382707377857, 2.0353916150214837, 'UPHENO:0002826', 'abnormal dentition'),
(289738, 'HP:0100612', 'Odontogenic neoplasm', 'XPO:0103199', 'abnormal tongue morphology', 0.5423728813559322, 7.884497199543557, 2.0679307203480533, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(289739, 'HP:0100612', 'Odontogenic neoplasm', 'XPO:0140626', 'abnormally necrotic tongue', 0.5, 7.884497199543557, 1.9855096574360394, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(289740, 'HP:0100612', 'Odontogenic neoplasm', 'XPO:0130628', 'increased size of the oral cavity', 0.5, 7.884497199543557, 1.9855096574360394, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(289741, 'HP:0100612', 'Odontogenic neoplasm', 'XPO:0100647', 'abnormal mouth', 0.4339622641509434, 7.0866363731414825, 1.7536626715827954, 'HP:0000153', 'Abnormality of the mouth'),
(289742, 'HP:0100612', 'Odontogenic neoplasm', 'XPO:0141311', 'abnormal roof of mouth morphology', 0.4838709677419355, 7.312692920701687, 1.8810634758932314, 'UPHENO:0076800', 'abnormal mouth morphology'),
(289743, 'HP:0100612', 'Odontogenic neoplasm', 'XPO:0141006', 'abnormally necrotic cementum', 0.4111111111111111, 9.181382707377857, 1.9428248625047118, 'UPHENO:0002826', 'abnormal dentition'),
(289744, 'HP:0100612', 'Odontogenic neoplasm', 'XPO:0127103', 'abnormally localised upper jaw', 0.41935483870967744, 7.0866363731414825, 1.7238953718984455, 'HP:0000153', 'Abnormality of the mouth'),
(289745, 'HP:0100612', 'Odontogenic neoplasm', 'XPO:0100766', 'abnormal Meckels cartilage', 0.40625, 7.0866363731414825, 1.6967457165376099, 'HP:0000153', 'Abnormality of the mouth'),
(289746, 'HP:0100612', 'Odontogenic neoplasm', 'XPO:0129585', 'increased size of the tongue', 0.4342105263157895, 7.884497199543557, 1.8502788110847448, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(289747, 'HP:0100612', 'Odontogenic neoplasm', 'XPO:0102890', 'abnormal dentine morphology', 0.44047619047619047, 9.181382707377857, 2.0110147881728198, 'UPHENO:0002826', 'abnormal dentition'),
(289748, 'HP:0100612', 'Odontogenic neoplasm', 'XPO:0100027', 'abnormal lower jaw', 0.49056603773584906, 7.0866363731414825, 1.8645275880090284, 'HP:0000153', 'Abnormality of the mouth'),
(289749, 'HP:0100612', 'Odontogenic neoplasm', 'XPO:0127611', 'abnormally localised lower jaw', 0.41935483870967744, 7.0866363731414825, 1.7238953718984455, 'HP:0000153', 'Abnormality of the mouth'),
(289750, 'HP:0100612', 'Odontogenic neoplasm', 'XPO:0129152', 'decreased size of the oral cavity', 0.5, 7.884497199543557, 1.9855096574360394, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(289751, 'HP:0100612', 'Odontogenic neoplasm', 'XPO:0101464', 'abnormal oral cavity', 0.42592592592592593, 7.0866363731414825, 1.7373491758799184, 'HP:0000153', 'Abnormality of the mouth'),
(289752, 'HP:0001328', 'Specific learning disability', 'XPO:0100702', 'abnormal glial cell', 0.43333333333333335, 3.94131651835137, 1.3068679445984308, 'UPHENO:0004523', 'abnormal nervous system'),
(289753, 'HP:0001328', 'Specific learning disability', 'XPO:0101132', 'abnormal apoptotic cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(289754, 'HP:0001328', 'Specific learning disability', 'XPO:0100285', 'abnormal progenitor cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(289755, 'HP:0001328', 'Specific learning disability', 'XPO:0100864', 'abnormal dorsolateral ascending neuron', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(289756, 'HP:0001328', 'Specific learning disability', 'XPO:0101241', 'abnormal nucleate erythrocyte', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(289757, 'HP:0001328', 'Specific learning disability', 'XPO:0101333', 'abnormal barrier epithelial cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(289758, 'HP:0001328', 'Specific learning disability', 'XPO:0100704', 'abnormal Merkel cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(289759, 'HP:0001328', 'Specific learning disability', 'XPO:0100273', 'abnormal visual system', 0.4642857142857143, 3.94131651835137, 1.3527368387638634, 'UPHENO:0004523', 'abnormal nervous system'),
(289760, 'HP:0001328', 'Specific learning disability', 'XPO:0100858', 'abnormal presumptive midbrain-hindbrain boundary', 0.43333333333333335, 3.94131651835137, 1.3068679445984308, 'UPHENO:0004523', 'abnormal nervous system'),
(289761, 'HP:0001328', 'Specific learning disability', 'XPO:0100760', 'abnormal Stirnorgan', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(289762, 'HP:0001328', 'Specific learning disability', 'XPO:0100533', 'abnormal melanoblast', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(289763, 'HP:0001328', 'Specific learning disability', 'XPO:0100715', 'abnormal ciliated cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(289764, 'HP:0001328', 'Specific learning disability', 'XPO:0101187', 'abnormal dorsolateral commissural neuron', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(289765, 'HP:0001328', 'Specific learning disability', 'XPO:0101239', 'abnormal olfactory epithelial support cell', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(289766, 'HP:0001328', 'Specific learning disability', 'XPO:0100653', 'abnormal myoblast', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(289767, 'HP:0001328', 'Specific learning disability', 'XPO:0107253', 'abnormal enteric nervous system', 0.48148148148148145, 3.94131651835137, 1.3775597686645948, 'UPHENO:0004523', 'abnormal nervous system'),
(289768, 'HP:0001328', 'Specific learning disability', 'XPO:0100691', 'abnormal keratin accumulating cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(289769, 'HP:0001328', 'Specific learning disability', 'XPO:0100026', 'abnormal germ cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(289770, 'HP:0001328', 'Specific learning disability', 'XPO:0101237', 'abnormal mucus secreting cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(289771, 'HP:0001328', 'Specific learning disability', 'XPO:0100056', 'abnormal olfactory epithelium', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(289772, 'HP:0001328', 'Specific learning disability', 'XPO:0100172', 'abnormal stem cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(289773, 'HP:0001328', 'Specific learning disability', 'XPO:0100477', 'abnormal pericyte', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(289774, 'HP:0001328', 'Specific learning disability', 'XPO:0100175', 'abnormal migrating neuroblast', 0.43333333333333335, 3.94131651835137, 1.3068679445984308, 'UPHENO:0004523', 'abnormal nervous system'),
(289775, 'HP:0001328', 'Specific learning disability', 'XPO:0100852', 'abnormal interdigital region', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(289776, 'HP:0001328', 'Specific learning disability', 'XPO:0142051', 'abnormal cerebrospinal fluid', 0.4482758620689655, 3.94131651835137, 1.3292091859262085, 'UPHENO:0004523', 'abnormal nervous system'),
(289777, 'HP:0001328', 'Specific learning disability', 'XPO:0100108', 'abnormal cell part', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(289778, 'HP:0001328', 'Specific learning disability', 'XPO:0100196', 'abnormal neuron', 0.43333333333333335, 3.94131651835137, 1.3068679445984308, 'UPHENO:0004523', 'abnormal nervous system'),
(289779, 'HP:0001328', 'Specific learning disability', 'XPO:0100734', 'abnormal lateral line system', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(289780, 'HP:0001328', 'Specific learning disability', 'XPO:0100114', 'abnormal peripheral nervous system', 0.4482758620689655, 3.94131651835137, 1.3292091859262085, 'UPHENO:0004523', 'abnormal nervous system'),
(289781, 'HP:0001328', 'Specific learning disability', 'XPO:0107287', 'abnormal afferent neuron', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(289782, 'HP:0001328', 'Specific learning disability', 'XPO:0100158', 'abnormal neuromere', 0.43333333333333335, 3.94131651835137, 1.3068679445984308, 'UPHENO:0004523', 'abnormal nervous system'),
(289783, 'HP:0001328', 'Specific learning disability', 'XPO:0100358', 'abnormal ganglion', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(289784, 'HP:0001328', 'Specific learning disability', 'XPO:0101435', 'abnormal paracrine cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(289785, 'HP:0001328', 'Specific learning disability', 'XPO:0100274', 'abnormal sensory system', 0.48148148148148145, 3.94131651835137, 1.3775597686645948, 'UPHENO:0004523', 'abnormal nervous system'),
(289786, 'HP:0001328', 'Specific learning disability', 'XPO:0100642', 'abnormal gustatory system', 0.4642857142857143, 3.94131651835137, 1.3527368387638634, 'UPHENO:0004523', 'abnormal nervous system'),
(289787, 'HP:0001328', 'Specific learning disability', 'XPO:0100754', 'abnormal electrically active cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(289788, 'HP:0001328', 'Specific learning disability', 'XPO:0100802', 'abnormal exocrine cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(289789, 'HP:0001328', 'Specific learning disability', 'XPO:0101448', 'abnormal myelin accumulating cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(289790, 'HP:0001328', 'Specific learning disability', 'XPO:0126887', 'abnormally localised nervous system', 0.4117647058823529, 3.94131651835137, 1.2739289764222381, 'UPHENO:0004523', 'abnormal nervous system'),
(289791, 'HP:0001328', 'Specific learning disability', 'XPO:0101467', 'abnormal alkali secreting cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(289792, 'HP:0001328', 'Specific learning disability', 'XPO:0100004', 'abnormal cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(289793, 'HP:0001328', 'Specific learning disability', 'XPO:0101535', 'abnormal absorptive cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(289794, 'HP:0001328', 'Specific learning disability', 'XPO:0100289', 'abnormal chondroblast', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(289795, 'HP:0001328', 'Specific learning disability', 'XPO:0100006', 'abnormal anatomical structure', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289796, 'HP:0001328', 'Specific learning disability', 'XPO:0101373', 'abnormal oxygen accumulating cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(289797, 'HP:0001328', 'Specific learning disability', 'XPO:0100587', 'abnormal vestibuloauditory system', 0.4642857142857143, 3.94131651835137, 1.3527368387638634, 'UPHENO:0004523', 'abnormal nervous system'),
(289798, 'HP:0001328', 'Specific learning disability', 'XPO:0100081', 'abnormal anatomical entity in vitro', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289799, 'HP:0001328', 'Specific learning disability', 'XPO:0101297', 'abnormal barrier cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(289800, 'HP:0001328', 'Specific learning disability', 'XPO:0100481', 'abnormal anatomical line', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289801, 'HP:0001328', 'Specific learning disability', 'XPO:0100031', 'abnormal central nervous system', 0.48148148148148145, 3.94131651835137, 1.3775597686645948, 'UPHENO:0004523', 'abnormal nervous system'),
(289802, 'HP:0001328', 'Specific learning disability', 'XPO:0100549', 'abnormal mitotic cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(289803, 'HP:0001328', 'Specific learning disability', 'XPO:0100427', 'abnormal olfactory system', 0.4642857142857143, 3.94131651835137, 1.3527368387638634, 'UPHENO:0004523', 'abnormal nervous system'),
(289804, 'HP:0001328', 'Specific learning disability', 'XPO:0101501', 'abnormal parabrachial area', 0.43333333333333335, 3.94131651835137, 1.3068679445984308, 'UPHENO:0004523', 'abnormal nervous system'),
(289805, 'HP:0001328', 'Specific learning disability', 'XPO:0100438', 'abnormal spinal cord', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(289806, 'HP:0001328', 'Specific learning disability', 'XPO:0100791', 'abnormal multiciliated cell precursor', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(289807, 'HP:0001328', 'Specific learning disability', 'XPO:0100337', 'abnormal zygote', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(289808, 'HP:0001328', 'Specific learning disability', 'XPO:0100344', 'abnormal portion of organism substance', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(289809, 'HP:0001328', 'Specific learning disability', 'XPO:0100954', 'abnormal neural progenitor cell', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(289810, 'HP:0001328', 'Specific learning disability', 'XPO:0100537', 'abnormal medium cavity', 0.43333333333333335, 3.94131651835137, 1.3068679445984308, 'UPHENO:0004523', 'abnormal nervous system'),
(289811, 'HP:0001328', 'Specific learning disability', 'XPO:0101326', 'abnormal cementoblast', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(289812, 'HP:0001328', 'Specific learning disability', 'XPO:0107286', 'abnormal efferent neuron', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(289813, 'HP:0001328', 'Specific learning disability', 'XPO:0100032', 'abnormal nervous system', 0.5, 3.94131651835137, 1.4038013602984167, 'UPHENO:0004523', 'abnormal nervous system'),
(289814, 'HP:0001328', 'Specific learning disability', 'XPO:0100164', 'abnormal neural nucleus', 0.4482758620689655, 3.94131651835137, 1.3292091859262085, 'UPHENO:0004523', 'abnormal nervous system'),
(289815, 'HP:0001328', 'Specific learning disability', 'XPO:0131654', 'abnormal neuron projection', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(289816, 'HP:0001328', 'Specific learning disability', 'XPO:0101004', 'abnormal acid secreting cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(289817, 'HP:0001328', 'Specific learning disability', 'XPO:0100336', 'abnormal interneuron', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(289818, 'HP:0001328', 'Specific learning disability', 'XPO:0100638', 'abnormal polar body', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(289819, 'HP:0001328', 'Specific learning disability', 'XPO:0100701', 'abnormal microglial cell', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(289820, 'HP:0001328', 'Specific learning disability', 'XPO:0101133', 'abnormal motor neuron', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(289821, 'HP:0001328', 'Specific learning disability', 'XPO:0100916', 'abnormal principal cavity', 0.43333333333333335, 3.94131651835137, 1.3068679445984308, 'UPHENO:0004523', 'abnormal nervous system'),
(289822, 'HP:0005262', 'Abnormal synovial membrane morphology', 'XPO:0101586', 'abnormal joint', 0.42424242424242425, 4.3395673355180735, 1.3568450783281876, 'UPHENO:0002964', 'abnormal skeletal system'),
(289823, 'HP:0005262', 'Abnormal synovial membrane morphology', 'XPO:0101957', 'abnormal axial skeleton morphology', 0.4146341463414634, 4.638757693672553, 1.3868624071625903, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(289824, 'HP:0005262', 'Abnormal synovial membrane morphology', 'XPO:0107372', 'abnormal flexural organ morphology', 0.4594594594594595, 4.638757693672553, 1.4599044840325002, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(289825, 'HP:0005262', 'Abnormal synovial membrane morphology', 'XPO:0130368', 'increased size of the elastica externa', 0.40476190476190477, 4.638757693672553, 1.3702526773627712, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(289826, 'HP:0005262', 'Abnormal synovial membrane morphology', 'XPO:0107285', 'abnormal flexural organ', 0.4827586206896552, 4.3395673355180735, 1.4473988881039626, 'UPHENO:0002964', 'abnormal skeletal system'),
(289827, 'HP:0005262', 'Abnormal synovial membrane morphology', 'XPO:0140683', 'abnormally necrotic flexural organ', 0.40476190476190477, 4.638757693672553, 1.3702526773627712, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(289828, 'HP:0005262', 'Abnormal synovial membrane morphology', 'XPO:0101348', 'abnormal perichordal tissue', 0.4375, 4.3395673355180735, 1.3778826906849353, 'UPHENO:0002964', 'abnormal skeletal system'),
(289829, 'HP:0005262', 'Abnormal synovial membrane morphology', 'XPO:0101982', 'abnormal appendicular skeleton morphology', 0.40476190476190477, 4.638757693672553, 1.3702526773627712, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(289830, 'HP:0005262', 'Abnormal synovial membrane morphology', 'XPO:0128352', 'decreased size of the skeletal system', 0.40476190476190477, 4.638757693672553, 1.3702526773627712, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(289831, 'HP:0005262', 'Abnormal synovial membrane morphology', 'XPO:0100512', 'abnormal cranial skeleton', 0.42424242424242425, 4.3395673355180735, 1.3568450783281876, 'UPHENO:0002964', 'abnormal skeletal system'),
(289832, 'HP:0005262', 'Abnormal synovial membrane morphology', 'XPO:0100350', 'abnormal appendicular skeleton', 0.4375, 4.3395673355180735, 1.3778826906849353, 'UPHENO:0002964', 'abnormal skeletal system'),
(289833, 'HP:0005262', 'Abnormal synovial membrane morphology', 'XPO:0100882', 'abnormal perichondrial cell', 0.4117647058823529, 4.3395673355180735, 1.3367425584480601, 'UPHENO:0002964', 'abnormal skeletal system'),
(289834, 'HP:0005262', 'Abnormal synovial membrane morphology', 'XPO:0102980', 'abnormal perichordal tissue morphology', 0.4146341463414634, 4.638757693672553, 1.3868624071625903, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(289835, 'HP:0005262', 'Abnormal synovial membrane morphology', 'XPO:0102054', 'abnormal notochord morphology', 0.4594594594594595, 4.638757693672553, 1.4599044840325002, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(289836, 'HP:0005262', 'Abnormal synovial membrane morphology', 'XPO:0100004', 'abnormal cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(289837, 'HP:0005262', 'Abnormal synovial membrane morphology', 'XPO:0102130', 'abnormal endoskeleton morphology', 0.425, 4.638757693672553, 1.404091172186064, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(289838, 'HP:0005262', 'Abnormal synovial membrane morphology', 'XPO:0139774', 'abnormally necrotic elastica externa', 0.425, 4.638757693672553, 1.404091172186064, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(289839, 'HP:0005262', 'Abnormal synovial membrane morphology', 'XPO:0100325', 'abnormal axial skeleton', 0.4375, 4.3395673355180735, 1.3778826906849353, 'UPHENO:0002964', 'abnormal skeletal system'),
(289840, 'HP:0005262', 'Abnormal synovial membrane morphology', 'XPO:0140432', 'abnormally necrotic skeleton', 0.40476190476190477, 4.638757693672553, 1.3702526773627712, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(289841, 'HP:0005262', 'Abnormal synovial membrane morphology', 'XPO:0102514', 'abnormal perichondrial cell morphology', 0.40476190476190477, 4.638757693672553, 1.3702526773627712, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(289842, 'HP:0005262', 'Abnormal synovial membrane morphology', 'XPO:0100935', 'abnormal skeleton', 0.4666666666666667, 4.3395673355180735, 1.4230711237467255, 'UPHENO:0002964', 'abnormal skeletal system'),
(289843, 'HP:0005262', 'Abnormal synovial membrane morphology', 'XPO:0101860', 'abnormal skeletal subdivision morphology', 0.4473684210526316, 4.638757693672553, 1.4405671470167702, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(289844, 'HP:0005262', 'Abnormal synovial membrane morphology', 'XPO:0140350', 'abnormally necrotic notochordal sheath', 0.40476190476190477, 4.638757693672553, 1.3702526773627712, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(289845, 'HP:0005262', 'Abnormal synovial membrane morphology', 'XPO:0102806', 'abnormal articular system morphology', 0.4722222222222222, 4.638757693672553, 1.4800420488812078, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(289846, 'HP:0005262', 'Abnormal synovial membrane morphology', 'XPO:0102144', 'abnormal cranial skeleton morphology', 0.40476190476190477, 4.638757693672553, 1.3702526773627712, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(289847, 'HP:0005262', 'Abnormal synovial membrane morphology', 'XPO:0102567', 'abnormal skeleton morphology', 0.4594594594594595, 4.638757693672553, 1.4599044840325002, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(289848, 'HP:0005262', 'Abnormal synovial membrane morphology', 'XPO:0101174', 'abnormal articular system', 0.4827586206896552, 4.3395673355180735, 1.4473988881039626, 'UPHENO:0002964', 'abnormal skeletal system'),
(289849, 'HP:0005262', 'Abnormal synovial membrane morphology', 'XPO:0100829', 'abnormal postcranial axial skeleton', 0.42424242424242425, 4.3395673355180735, 1.3568450783281876, 'UPHENO:0002964', 'abnormal skeletal system'),
(289850, 'HP:0005262', 'Abnormal synovial membrane morphology', 'XPO:0100910', 'abnormal vacuolated notochordal tissue', 0.4375, 4.3395673355180735, 1.3778826906849353, 'UPHENO:0002964', 'abnormal skeletal system'),
(289851, 'HP:0005262', 'Abnormal synovial membrane morphology', 'XPO:0141718', 'abnormal posterior notochord', 0.4827586206896552, 4.3395673355180735, 1.4473988881039626, 'UPHENO:0002964', 'abnormal skeletal system'),
(289852, 'HP:0005262', 'Abnormal synovial membrane morphology', 'XPO:0100465', 'abnormal skeletal system', 0.5, 4.3395673355180735, 1.473018556488355, 'UPHENO:0002964', 'abnormal skeletal system'),
(289853, 'HP:0005262', 'Abnormal synovial membrane morphology', 'XPO:0141719', 'abnormal anterior notochord morphology', 0.4594594594594595, 4.638757693672553, 1.4599044840325002, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(289854, 'HP:0005262', 'Abnormal synovial membrane morphology', 'XPO:0100498', 'abnormal endoskeleton', 0.4375, 4.3395673355180735, 1.3778826906849353, 'UPHENO:0002964', 'abnormal skeletal system'),
(289855, 'HP:0005262', 'Abnormal synovial membrane morphology', 'XPO:0103218', 'abnormal joint morphology', 0.4634146341463415, 8.100914173390091, 1.9375454002196908, 'UPHENO:0076767', 'abnormal skeletal joint morphology'),
(289856, 'HP:0005262', 'Abnormal synovial membrane morphology', 'XPO:0100123', 'abnormal pelvic girdle', 0.42424242424242425, 4.3395673355180735, 1.3568450783281876, 'UPHENO:0002964', 'abnormal skeletal system'),
(289857, 'HP:0005262', 'Abnormal synovial membrane morphology', 'XPO:0101484', 'abnormal bone marrow', 0.4117647058823529, 4.3395673355180735, 1.3367425584480601, 'UPHENO:0002964', 'abnormal skeletal system'),
(289858, 'HP:0005262', 'Abnormal synovial membrane morphology', 'XPO:0140559', 'abnormally necrotic articular system', 0.4146341463414634, 4.638757693672553, 1.3868624071625903, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(289859, 'HP:0005262', 'Abnormal synovial membrane morphology', 'XPO:0141699', 'abnormally necrotic anterior notochord', 0.40476190476190477, 4.638757693672553, 1.3702526773627712, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(289860, 'HP:0005262', 'Abnormal synovial membrane morphology', 'XPO:0100584', 'abnormal vertebral column', 0.40476190476190477, 4.638757693672553, 1.3702526773627712, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(289861, 'HP:0005262', 'Abnormal synovial membrane morphology', 'XPO:0140565', 'abnormally necrotic joint', 0.41304347826086957, 8.100914173390091, 1.8292156153034065, 'UPHENO:0076767', 'abnormal skeletal joint morphology'),
(289862, 'HP:0005262', 'Abnormal synovial membrane morphology', 'XPO:0100640', 'abnormal notochordal sheath', 0.4827586206896552, 4.3395673355180735, 1.4473988881039626, 'UPHENO:0002964', 'abnormal skeletal system'),
(289863, 'HP:0005262', 'Abnormal synovial membrane morphology', 'XPO:0100422', 'abnormal notochord', 0.5, 4.3395673355180735, 1.473018556488355, 'UPHENO:0002964', 'abnormal skeletal system'),
(289864, 'HP:0005262', 'Abnormal synovial membrane morphology', 'XPO:0102010', 'abnormal perichondrium morphology', 0.4473684210526316, 4.638757693672553, 1.4405671470167702, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(289865, 'HP:0005262', 'Abnormal synovial membrane morphology', 'XPO:0140019', 'abnormally necrotic skeletal system', 0.425, 4.638757693672553, 1.404091172186064, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(289866, 'HP:0005262', 'Abnormal synovial membrane morphology', 'XPO:0128890', 'decreased size of the elastica externa', 0.40476190476190477, 4.638757693672553, 1.3702526773627712, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(289867, 'HP:0005262', 'Abnormal synovial membrane morphology', 'XPO:0100973', 'abnormal dermal skeleton', 0.4375, 4.3395673355180735, 1.3778826906849353, 'UPHENO:0002964', 'abnormal skeletal system'),
(289868, 'HP:0005262', 'Abnormal synovial membrane morphology', 'XPO:0102097', 'abnormal skeletal system morphology', 0.4857142857142857, 4.638757693672553, 1.5010366017468766, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(289869, 'HP:0005262', 'Abnormal synovial membrane morphology', 'XPO:0102542', 'abnormal vacuolated notochordal tissue morphology', 0.4146341463414634, 4.638757693672553, 1.3868624071625903, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(289870, 'HP:0005262', 'Abnormal synovial membrane morphology', 'XPO:0100378', 'abnormal perichondrium', 0.4666666666666667, 4.3395673355180735, 1.4230711237467255, 'UPHENO:0002964', 'abnormal skeletal system'),
(289871, 'HP:0005262', 'Abnormal synovial membrane morphology', 'XPO:0141703', 'abnormally necrotic posterior notochord', 0.40476190476190477, 4.638757693672553, 1.3702526773627712, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(289872, 'HP:0005262', 'Abnormal synovial membrane morphology', 'XPO:0100585', 'abnormal elastica externa', 0.5185185185185185, 4.3395673355180735, 1.5000486744849937, 'UPHENO:0002964', 'abnormal skeletal system'),
(289873, 'HP:0005262', 'Abnormal synovial membrane morphology', 'XPO:0100377', 'abnormal connective tissue', 0.41379310344827586, 3.9037819259951223, 1.270967363209146, 'HP:0033127', 'Abnormality of the musculoskeletal system'),
(289874, 'HP:0005262', 'Abnormal synovial membrane morphology', 'XPO:0129832', 'increased size of the skeletal system', 0.40476190476190477, 4.638757693672553, 1.3702526773627712, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(289875, 'HP:0005262', 'Abnormal synovial membrane morphology', 'XPO:0100228', 'abnormal skeletal subdivision', 0.45161290322580644, 4.3395673355180735, 1.399930213666808, 'UPHENO:0002964', 'abnormal skeletal system'),
(289876, 'HP:0005262', 'Abnormal synovial membrane morphology', 'XPO:0141714', 'abnormal anterior notochord', 0.4827586206896552, 4.3395673355180735, 1.4473988881039626, 'UPHENO:0002964', 'abnormal skeletal system'),
(289877, 'HP:0005262', 'Abnormal synovial membrane morphology', 'XPO:0100461', 'abnormal craniofacial skeleton', 0.4117647058823529, 4.3395673355180735, 1.3367425584480601, 'UPHENO:0002964', 'abnormal skeletal system'),
(289878, 'HP:0005262', 'Abnormal synovial membrane morphology', 'XPO:0102217', 'abnormal elastica externa morphology', 0.4857142857142857, 4.638757693672553, 1.5010366017468766, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(289879, 'HP:0005262', 'Abnormal synovial membrane morphology', 'XPO:0141723', 'abnormal posterior notochord morphology', 0.4594594594594595, 4.638757693672553, 1.4599044840325002, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(289880, 'HP:0005262', 'Abnormal synovial membrane morphology', 'XPO:0102605', 'abnormal dermal skeleton morphology', 0.425, 4.638757693672553, 1.404091172186064, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(289881, 'HP:0005262', 'Abnormal synovial membrane morphology', 'XPO:0102272', 'abnormal notochordal sheath morphology', 0.4594594594594595, 4.638757693672553, 1.4599044840325002, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(289882, 'HP:6000531', 'Abnormal urinary organic compound level', 'XPO:0100069', 'abnormal urinary system', 0.4838709677419355, 6.355235291121788, 1.7536002539184354, 'HP:0000079', 'Abnormality of the urinary system'),
(289883, 'HP:6000531', 'Abnormal urinary organic compound level', 'XPO:0100501', 'abnormal urogenital system', 0.43333333333333335, 5.4478002382576385, 1.5364613358553185, 'HP:0000119', 'Abnormality of the genitourinary system'),
(289884, 'HP:6000531', 'Abnormal urinary organic compound level', 'XPO:0101701', 'abnormal urinary system morphology', 0.41025641025641024, 6.355235291121788, 1.61470617044417, 'HP:0000079', 'Abnormality of the urinary system'),
(289885, 'HP:6000531', 'Abnormal urinary organic compound level', 'XPO:0126535', 'abnormally localised urinary system', 0.41025641025641024, 6.355235291121788, 1.61470617044417, 'HP:0000079', 'Abnormality of the urinary system'),
(289886, 'HP:6000531', 'Abnormal urinary organic compound level', 'XPO:0100085', 'abnormal mesonephric sinus', 0.4166666666666667, 6.355235291121788, 1.6272721667361236, 'HP:0000079', 'Abnormality of the urinary system'),
(289887, 'HP:0033050', 'Pharyngalgia', 'XPO:0128419', 'decreased size of the pharynx', 0.5, 8.127241455820435, 2.0158424362807272, 'HP:0000600', 'Abnormality of the pharynx'),
(289888, 'HP:0033050', 'Pharyngalgia', 'XPO:0100586', 'abnormal thyroid primordium', 0.6153846153846154, 8.127241455820435, 2.2363763899281266, 'HP:0000600', 'Abnormality of the pharynx'),
(289889, 'HP:0033050', 'Pharyngalgia', 'XPO:0126876', 'abnormally localised aortic arch', 0.45714285714285713, 8.127241455820435, 1.9275140414024556, 'HP:0000600', 'Abnormality of the pharynx'),
(289890, 'HP:0033050', 'Pharyngalgia', 'XPO:0141644', 'neoplastic larynx', 0.4262295081967213, 7.783689670920507, 1.821438503049814, 'HP:0002087', 'Abnormality of the upper respiratory tract'),
(289891, 'HP:0033050', 'Pharyngalgia', 'XPO:0100262', 'abnormal aortic arch 4', 0.5333333333333333, 8.127241455820435, 2.0819531158115847, 'HP:0000600', 'Abnormality of the pharynx'),
(289892, 'HP:0033050', 'Pharyngalgia', 'XPO:0125763', 'absent thyroid primordium', 0.49230769230769234, 8.127241455820435, 2.000275852461947, 'HP:0000600', 'Abnormality of the pharynx'),
(289893, 'HP:0033050', 'Pharyngalgia', 'XPO:0100360', 'abnormal aortic arch 6', 0.5333333333333333, 8.127241455820435, 2.0819531158115847, 'HP:0000600', 'Abnormality of the pharynx'),
(289894, 'HP:0033050', 'Pharyngalgia', 'XPO:0140110', 'abnormally necrotic pharynx', 0.5245901639344263, 8.127241455820435, 2.064817407821696, 'HP:0000600', 'Abnormality of the pharynx'),
(289895, 'HP:0033050', 'Pharyngalgia', 'XPO:0128494', 'decreased size of the oropharynx', 0.45714285714285713, 8.127241455820435, 1.9275140414024556, 'HP:0000600', 'Abnormality of the pharynx'),
(289896, 'HP:0033050', 'Pharyngalgia', 'XPO:0100804', 'abnormal larynx', 0.52, 7.783689670920507, 2.0118445836790335, 'HP:0002087', 'Abnormality of the upper respiratory tract'),
(289897, 'HP:0033050', 'Pharyngalgia', 'XPO:0102668', 'abnormal pharynx morphology', 0.5714285714285714, 8.127241455820435, 2.1550262120806174, 'HP:0000600', 'Abnormality of the pharynx'),
(289898, 'HP:0033050', 'Pharyngalgia', 'XPO:0125326', 'absent oropharynx', 0.5245901639344263, 8.127241455820435, 2.064817407821696, 'HP:0000600', 'Abnormality of the pharynx'),
(289899, 'HP:0033050', 'Pharyngalgia', 'XPO:0101949', 'abnormal respiratory system morphology', 0.5106382978723404, 7.241224942262181, 1.922926618211807, 'HP:0012252', 'Abnormal respiratory system morphology'),
(289900, 'HP:0033050', 'Pharyngalgia', 'XPO:0125232', 'absent pharynx', 0.5614035087719298, 8.127241455820435, 2.1360388268789214, 'HP:0000600', 'Abnormality of the pharynx'),
(289901, 'HP:0033050', 'Pharyngalgia', 'XPO:0130015', 'increased size of the respiratory system', 0.4444444444444444, 7.241224942262181, 1.793968281927239, 'HP:0012252', 'Abnormal respiratory system morphology'),
(289902, 'HP:0033050', 'Pharyngalgia', 'XPO:0100116', 'abnormal aortic arch 1', 0.5333333333333333, 8.127241455820435, 2.0819531158115847, 'HP:0000600', 'Abnormality of the pharynx'),
(289903, 'HP:0033050', 'Pharyngalgia', 'XPO:0128944', 'decreased size of the pharyngeal epithelium', 0.4444444444444444, 8.127241455820435, 1.900554475330284, 'HP:0000600', 'Abnormality of the pharynx'),
(289904, 'HP:0033050', 'Pharyngalgia', 'XPO:0126855', 'abnormally localised pharynx', 0.5714285714285714, 8.127241455820435, 2.1550262120806174, 'HP:0000600', 'Abnormality of the pharynx'),
(289905, 'HP:0033050', 'Pharyngalgia', 'XPO:0101036', 'abnormal pharynx', 0.6666666666666666, 8.127241455820435, 2.3276943464610977, 'HP:0000600', 'Abnormality of the pharynx'),
(289906, 'HP:0033050', 'Pharyngalgia', 'XPO:0127859', 'abnormally localised larynx', 0.43333333333333335, 7.783689670920507, 1.8365544344593274, 'HP:0002087', 'Abnormality of the upper respiratory tract'),
(289907, 'HP:0033050', 'Pharyngalgia', 'XPO:0130422', 'increased size of the pharyngeal epithelium', 0.4444444444444444, 8.127241455820435, 1.900554475330284, 'HP:0000600', 'Abnormality of the pharynx'),
(289908, 'HP:0033050', 'Pharyngalgia', 'XPO:0100875', 'abnormal oropharynx', 0.6274509803921569, 8.127241455820435, 2.2581952128499236, 'HP:0000600', 'Abnormality of the pharynx'),
(289909, 'HP:0033050', 'Pharyngalgia', 'XPO:0126957', 'abnormally localised aortic arch 4', 0.4444444444444444, 8.127241455820435, 1.900554475330284, 'HP:0000600', 'Abnormality of the pharynx'),
(289910, 'HP:0033050', 'Pharyngalgia', 'XPO:0126955', 'abnormally localised oropharynx', 0.5423728813559322, 8.127241455820435, 2.0995226519065495, 'HP:0000600', 'Abnormality of the pharynx'),
(289911, 'HP:0033050', 'Pharyngalgia', 'XPO:0127174', 'abnormally localised aortic arch 1', 0.4444444444444444, 8.127241455820435, 1.900554475330284, 'HP:0000600', 'Abnormality of the pharynx'),
(289912, 'HP:0033050', 'Pharyngalgia', 'XPO:0125250', 'absent aortic arch 5', 0.4266666666666667, 8.127241455820435, 1.8621554771688782, 'HP:0000600', 'Abnormality of the pharynx'),
(289913, 'HP:0033050', 'Pharyngalgia', 'XPO:0127194', 'abnormally localised aortic arch 2', 0.4444444444444444, 8.127241455820435, 1.900554475330284, 'HP:0000600', 'Abnormality of the pharynx'),
(289914, 'HP:0033050', 'Pharyngalgia', 'XPO:0129899', 'increased size of the pharynx', 0.5079365079365079, 8.127241455820435, 2.0317781975959512, 'HP:0000600', 'Abnormality of the pharynx'),
(289915, 'HP:0033050', 'Pharyngalgia', 'XPO:0128535', 'decreased size of the respiratory system', 0.4444444444444444, 7.241224942262181, 1.793968281927239, 'HP:0012252', 'Abnormal respiratory system morphology'),
(289916, 'HP:0033050', 'Pharyngalgia', 'XPO:0125387', 'absent aortic arch 3', 0.42105263157894735, 8.127241455820435, 1.8498638875470566, 'HP:0000600', 'Abnormality of the pharynx'),
(289917, 'HP:0033050', 'Pharyngalgia', 'XPO:0141614', 'metaplastic larynx', 0.49056603773584906, 7.783689670920507, 1.954076201387481, 'HP:0002087', 'Abnormality of the upper respiratory tract'),
(289918, 'HP:0033050', 'Pharyngalgia', 'XPO:0126197', 'absent larynx', 0.4262295081967213, 7.783689670920507, 1.821438503049814, 'HP:0002087', 'Abnormality of the upper respiratory tract'),
(289919, 'HP:0033050', 'Pharyngalgia', 'XPO:0129974', 'increased size of the oropharynx', 0.45714285714285713, 8.127241455820435, 1.9275140414024556, 'HP:0000600', 'Abnormality of the pharynx'),
(289920, 'HP:0033050', 'Pharyngalgia', 'XPO:0129112', 'decreased size of the thyroid primordium', 0.4155844155844156, 8.127241455820435, 1.8378125287228213, 'HP:0000600', 'Abnormality of the pharynx'),
(289921, 'HP:0033050', 'Pharyngalgia', 'XPO:0125328', 'absent aortic arch 4', 0.42105263157894735, 8.127241455820435, 1.8498638875470566, 'HP:0000600', 'Abnormality of the pharynx'),
(289922, 'HP:0033050', 'Pharyngalgia', 'XPO:0125251', 'absent aortic arch', 0.4383561643835616, 8.127241455820435, 1.8874920904715122, 'HP:0000600', 'Abnormality of the pharynx'),
(289923, 'HP:0033050', 'Pharyngalgia', 'XPO:0140301', 'abnormally necrotic pharyngeal epithelium', 0.45714285714285713, 8.127241455820435, 1.9275140414024556, 'HP:0000600', 'Abnormality of the pharynx'),
(289924, 'HP:0033050', 'Pharyngalgia', 'XPO:0125599', 'absent pharyngeal epithelium', 0.5245901639344263, 8.127241455820435, 2.064817407821696, 'HP:0000600', 'Abnormality of the pharynx'),
(289925, 'HP:0033050', 'Pharyngalgia', 'XPO:0127240', 'abnormally localised pharyngeal epithelium', 0.5245901639344263, 8.127241455820435, 2.064817407821696, 'HP:0000600', 'Abnormality of the pharynx'),
(289926, 'HP:0033050', 'Pharyngalgia', 'XPO:0102436', 'abnormal larynx morphology', 0.4482758620689655, 7.783689670920507, 1.8679508016297413, 'HP:0002087', 'Abnormality of the upper respiratory tract'),
(289927, 'HP:0033050', 'Pharyngalgia', 'XPO:0127022', 'abnormally localised aortic arch 3', 0.4444444444444444, 8.127241455820435, 1.900554475330284, 'HP:0000600', 'Abnormality of the pharynx'),
(289928, 'HP:0033050', 'Pharyngalgia', 'XPO:0139850', 'abnormally necrotic respiratory system', 0.46153846153846156, 7.241224942262181, 1.8281421770490451, 'HP:0012252', 'Abnormal respiratory system morphology'),
(289929, 'HP:0033050', 'Pharyngalgia', 'XPO:0101395', 'abnormal m. geniohyoideus', 0.4383561643835616, 8.127241455820435, 1.8874920904715122, 'HP:0000600', 'Abnormality of the pharynx'),
(289930, 'HP:0033050', 'Pharyngalgia', 'XPO:0140398', 'abnormally necrotic thyroid primordium', 0.42105263157894735, 8.127241455820435, 1.8498638875470566, 'HP:0000600', 'Abnormality of the pharynx'),
(289931, 'HP:0033050', 'Pharyngalgia', 'XPO:0125557', 'absent aortic arch 2', 0.42105263157894735, 8.127241455820435, 1.8498638875470566, 'HP:0000600', 'Abnormality of the pharynx'),
(289932, 'HP:0033050', 'Pharyngalgia', 'XPO:0102507', 'abnormal oropharynx morphology', 0.5079365079365079, 8.127241455820435, 2.0317781975959512, 'HP:0000600', 'Abnormality of the pharynx'),
(289933, 'HP:0033050', 'Pharyngalgia', 'XPO:0102218', 'abnormal thyroid primordium morphology', 0.47761194029850745, 8.127241455820435, 1.9701948028022165, 'HP:0000600', 'Abnormality of the pharynx'),
(289934, 'HP:0033050', 'Pharyngalgia', 'XPO:0130588', 'increased size of the thyroid primordium', 0.4155844155844156, 8.127241455820435, 1.8378125287228213, 'HP:0000600', 'Abnormality of the pharynx'),
(289935, 'HP:0033050', 'Pharyngalgia', 'XPO:0126875', 'abnormally localised aortic arch 5', 0.4444444444444444, 8.127241455820435, 1.900554475330284, 'HP:0000600', 'Abnormality of the pharynx'),
(289936, 'HP:0033050', 'Pharyngalgia', 'XPO:0101210', 'abnormal aortic arch 2', 0.5333333333333333, 8.127241455820435, 2.0819531158115847, 'HP:0000600', 'Abnormality of the pharynx'),
(289937, 'HP:0033050', 'Pharyngalgia', 'XPO:0102961', 'abnormal pharyngeal epithelium morphology', 0.5161290322580645, 8.127241455820435, 2.048097963360206, 'HP:0000600', 'Abnormality of the pharynx'),
(289938, 'HP:0033050', 'Pharyngalgia', 'XPO:0127412', 'abnormally localised thyroid primordium', 0.5, 8.127241455820435, 2.0158424362807272, 'HP:0000600', 'Abnormality of the pharynx'),
(289939, 'HP:0033050', 'Pharyngalgia', 'XPO:0101474', 'abnormal aortic arch 5', 0.5333333333333333, 8.127241455820435, 2.0819531158115847, 'HP:0000600', 'Abnormality of the pharynx'),
(289940, 'HP:0033050', 'Pharyngalgia', 'XPO:0126690', 'abnormally localised aortic arch 6', 0.4444444444444444, 8.127241455820435, 1.900554475330284, 'HP:0000600', 'Abnormality of the pharynx'),
(289941, 'HP:0033050', 'Pharyngalgia', 'XPO:0100716', 'abnormal aortic arch 3', 0.5333333333333333, 8.127241455820435, 2.0819531158115847, 'HP:0000600', 'Abnormality of the pharynx'),
(289942, 'HP:0033050', 'Pharyngalgia', 'XPO:0125070', 'absent aortic arch 6', 0.42105263157894735, 8.127241455820435, 1.8498638875470566, 'HP:0000600', 'Abnormality of the pharynx'),
(289943, 'HP:0033050', 'Pharyngalgia', 'XPO:0101329', 'abnormal pharyngeal epithelium', 0.6530612244897959, 8.127241455820435, 2.303819927177974, 'HP:0000600', 'Abnormality of the pharynx'),
(289944, 'HP:0033050', 'Pharyngalgia', 'XPO:0125536', 'absent aortic arch 1', 0.4266666666666667, 8.127241455820435, 1.8621554771688782, 'HP:0000600', 'Abnormality of the pharynx'),
(289945, 'HP:0033050', 'Pharyngalgia', 'XPO:0141191', 'abnormally necrotic oropharynx', 0.47058823529411764, 8.127241455820435, 1.9556544210324416, 'HP:0000600', 'Abnormality of the pharynx'),
(289946, 'HP:0033050', 'Pharyngalgia', 'XPO:0100117', 'abnormal aortic arch', 0.5423728813559322, 8.127241455820435, 2.0995226519065495, 'HP:0000600', 'Abnormality of the pharynx'),
(289947, 'HP:0034348', 'Subpulmonary stenosis', 'XPO:0102769', 'abnormal cardiac valve morphology', 0.40625, 10.21769640676594, 2.0373853747508504, 'UPHENO:0015319', 'abnormal cardiac valve morphology in the heart'),
(289948, 'HP:0004783', 'Duodenal polyposis', 'XPO:0100361', 'abnormal small intestine', 0.47058823529411764, 8.518562886125473, 2.002182677935196, 'UPHENO:0076783', 'abnormal intestine morphology'),
(289949, 'HP:0004783', 'Duodenal polyposis', 'XPO:0102788', 'abnormal typhlosole morphology', 0.41379310344827586, 8.518562886125473, 1.8774777158648677, 'UPHENO:0076783', 'abnormal intestine morphology'),
(289950, 'HP:0004783', 'Duodenal polyposis', 'XPO:0101288', 'abnormal external coil of the small intestine', 0.46153846153846156, 8.518562886125473, 1.9828374640854927, 'UPHENO:0076783', 'abnormal intestine morphology'),
(289951, 'HP:0004783', 'Duodenal polyposis', 'XPO:0115391', 'abnormally undifferentiated alimentary system', 0.40540540540540543, 5.05060299610679, 1.4309233924911664, 'HP:0025031', 'Abnormality of the digestive system'),
(289952, 'HP:0004783', 'Duodenal polyposis', 'XPO:0101321', 'abnormal duodenum', 0.46153846153846156, 8.518562886125473, 1.9828374640854927, 'UPHENO:0076783', 'abnormal intestine morphology'),
(289953, 'HP:0004783', 'Duodenal polyposis', 'XPO:0107294', 'abnormal intestinal stem cell', 0.42857142857142855, 8.518562886125473, 1.9107099898944229, 'UPHENO:0076783', 'abnormal intestine morphology'),
(289954, 'HP:0004783', 'Duodenal polyposis', 'XPO:0101784', 'abnormal alimentary system morphology', 0.4186046511627907, 5.725717590856133, 1.5481640787645816, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(289955, 'HP:0004783', 'Duodenal polyposis', 'XPO:0100152', 'abnormal alimentary system', 0.4166666666666667, 5.05060299610679, 1.45066119926208, 'HP:0025031', 'Abnormality of the digestive system'),
(289956, 'HP:0004783', 'Duodenal polyposis', 'XPO:0107288', 'abnormal larval alimentary system', 0.40540540540540543, 5.05060299610679, 1.4309233924911664, 'HP:0025031', 'Abnormality of the digestive system'),
(289957, 'HP:0004783', 'Duodenal polyposis', 'XPO:0101471', 'abnormal rectum', 0.43636363636363634, 8.518562886125473, 1.928001835471643, 'UPHENO:0076783', 'abnormal intestine morphology'),
(289958, 'HP:0004783', 'Duodenal polyposis', 'XPO:0100493', 'abnormal liver and biliary system', 0.40540540540540543, 5.05060299610679, 1.4309233924911664, 'HP:0025031', 'Abnormality of the digestive system'),
(289959, 'HP:0004783', 'Duodenal polyposis', 'XPO:0101537', 'abnormal internal coil of the small intestine', 0.46153846153846156, 8.518562886125473, 1.9828374640854927, 'UPHENO:0076783', 'abnormal intestine morphology'),
(289960, 'HP:0004783', 'Duodenal polyposis', 'XPO:0101306', 'abnormal ileum', 0.46153846153846156, 8.518562886125473, 1.9828374640854927, 'UPHENO:0076783', 'abnormal intestine morphology'),
(289961, 'HP:0004783', 'Duodenal polyposis', 'XPO:0115392', 'abnormally incomplete structure of alimentary system', 0.4090909090909091, 5.725717590856133, 1.5304701939081158, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(289962, 'HP:0004783', 'Duodenal polyposis', 'XPO:0102522', 'abnormal pharyngeal cavity morphology', 0.4186046511627907, 5.725717590856133, 1.5481640787645816, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(289963, 'HP:0004783', 'Duodenal polyposis', 'XPO:0102473', 'abnormal large intestine morphology', 0.4067796610169492, 8.518562886125473, 1.8614988915306085, 'UPHENO:0076783', 'abnormal intestine morphology'),
(289964, 'HP:0004940', 'Generalized arterial calcification', 'XPO:0101711', 'abnormal dorsal aorta morphology', 0.4027777777777778, 9.01729298920255, 1.905771558126036, 'UPHENO:0015290', 'abnormal artery morphology in the independent continuant'),
(289965, 'HP:0004940', 'Generalized arterial calcification', 'XPO:0101780', 'abnormal arteria mesenterica posterior morphology', 0.4027777777777778, 9.01729298920255, 1.905771558126036, 'UPHENO:0015290', 'abnormal artery morphology in the independent continuant'),
(289966, 'HP:0004940', 'Generalized arterial calcification', 'XPO:0102875', 'abnormal vertebral artery morphology', 0.43333333333333335, 9.01729298920255, 1.976738128497156, 'UPHENO:0015290', 'abnormal artery morphology in the independent continuant'),
(289967, 'HP:0004940', 'Generalized arterial calcification', 'XPO:0139829', 'abnormally necrotic artery', 0.40625, 9.01729298920255, 1.9139684628706755, 'UPHENO:0015290', 'abnormal artery morphology in the independent continuant'),
(289968, 'HP:0004940', 'Generalized arterial calcification', 'XPO:0102421', 'abnormal occipitovertebral artery morphology', 0.43333333333333335, 9.01729298920255, 1.976738128497156, 'UPHENO:0015290', 'abnormal artery morphology in the independent continuant'),
(289969, 'HP:0004940', 'Generalized arterial calcification', 'XPO:0101774', 'abnormal paired dorsal aorta morphology', 0.43283582089552236, 9.01729298920255, 1.9756030505232889, 'UPHENO:0015290', 'abnormal artery morphology in the independent continuant'),
(289970, 'HP:0004940', 'Generalized arterial calcification', 'XPO:0102613', 'abnormal dorsal longitudinal anastomosing vessel morphology', 0.41379310344827586, 6.974839882869777, 1.6988645152534954, 'UPHENO:0087186', 'abnormal blood vessel morphology'),
(289971, 'HP:0004940', 'Generalized arterial calcification', 'XPO:0139803', 'abnormally necrotic aorta', 0.4027777777777778, 9.01729298920255, 1.905771558126036, 'UPHENO:0015290', 'abnormal artery morphology in the independent continuant'),
(289972, 'HP:0004940', 'Generalized arterial calcification', 'XPO:0102619', 'abnormal larval aorta morphology', 0.43333333333333335, 9.01729298920255, 1.976738128497156, 'UPHENO:0015290', 'abnormal artery morphology in the independent continuant'),
(289973, 'HP:0004940', 'Generalized arterial calcification', 'XPO:0102424', 'abnormal capillary morphology', 0.4098360655737705, 7.803720102857406, 1.788364041182337, 'HP:0033353', 'Abnormal blood vessel morphology'),
(289974, 'HP:0004940', 'Generalized arterial calcification', 'XPO:0102412', 'abnormal vascular plexus morphology', 0.43103448275862066, 9.077623523403872, 1.9780719805123057, 'UPHENO:0015321', 'abnormal vasculature morphology in the independent continuant'),
(289975, 'HP:0004940', 'Generalized arterial calcification', 'XPO:0101675', 'abnormal vein morphology', 0.4098360655737705, 7.803720102857406, 1.788364041182337, 'HP:0033353', 'Abnormal blood vessel morphology'),
(289976, 'HP:0004940', 'Generalized arterial calcification', 'XPO:0101712', 'abnormal aorta morphology', 0.4461538461538462, 9.01729298920255, 2.0057666736260304, 'UPHENO:0015290', 'abnormal artery morphology in the independent continuant'),
(289977, 'HP:0004940', 'Generalized arterial calcification', 'XPO:0101840', 'abnormal ventral aorta morphology', 0.4027777777777778, 9.01729298920255, 1.905771558126036, 'UPHENO:0015290', 'abnormal artery morphology in the independent continuant'),
(289978, 'HP:0004940', 'Generalized arterial calcification', 'XPO:0103063', 'abnormal ischiadic artery morphology', 0.43333333333333335, 9.01729298920255, 1.976738128497156, 'UPHENO:0015290', 'abnormal artery morphology in the independent continuant'),
(289979, 'HP:0004940', 'Generalized arterial calcification', 'XPO:0103091', 'abnormal arteria iliaca communis morphology', 0.4142857142857143, 9.01729298920255, 1.9328051290689765, 'UPHENO:0015290', 'abnormal artery morphology in the independent continuant'),
(289980, 'HP:0004940', 'Generalized arterial calcification', 'XPO:0102329', 'abnormal caudal artery morphology', 0.4084507042253521, 9.01729298920255, 1.9191455577016852, 'UPHENO:0015290', 'abnormal artery morphology in the independent continuant'),
(289981, 'HP:0004940', 'Generalized arterial calcification', 'XPO:0101708', 'abnormal artery morphology', 0.4482758620689655, 9.01729298920255, 2.010530971724438, 'UPHENO:0015290', 'abnormal artery morphology in the independent continuant'),
(289982, 'HP:0004940', 'Generalized arterial calcification', 'XPO:0101154', 'abnormal external carotid artery', 0.4117647058823529, 8.750570396338642, 1.8982033730744463, 'HP:0011004', 'Abnormal systemic arterial morphology'),
(289983, 'HP:0004940', 'Generalized arterial calcification', 'XPO:0103215', 'abnormal truncus arteriosus morphology', 0.41379310344827586, 6.974839882869777, 1.6988645152534954, 'UPHENO:0087186', 'abnormal blood vessel morphology'),
(289984, 'HP:0004940', 'Generalized arterial calcification', 'XPO:0101686', 'abnormal blood vessel morphology', 0.42857142857142855, 6.974839882869777, 1.7289352482549702, 'UPHENO:0087186', 'abnormal blood vessel morphology'),
(289985, 'HP:0031094', 'Abnormal breast physiology', 'XPO:0102980', 'abnormal perichordal tissue morphology', 0.43478260869565216, 4.638757693672553, 1.4201588541997616, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(289986, 'HP:0031094', 'Abnormal breast physiology', 'XPO:0129664', 'increased size of the skeleton', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(289987, 'HP:0031094', 'Abnormal breast physiology', 'XPO:0141709', 'increased size of the anterior notochord', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(289988, 'HP:0031094', 'Abnormal breast physiology', 'XPO:0140019', 'abnormally necrotic skeletal system', 0.4444444444444444, 4.638757693672553, 1.4358516936218344, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(289989, 'HP:0031094', 'Abnormal breast physiology', 'XPO:0140350', 'abnormally necrotic notochordal sheath', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(289990, 'HP:0031094', 'Abnormal breast physiology', 'XPO:0102401', 'abnormal neurocranium morphology', 0.40350877192982454, 6.272837960958401, 1.5909573036826314, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(289991, 'HP:0031094', 'Abnormal breast physiology', 'XPO:0102097', 'abnormal skeletal system morphology', 0.5, 4.638757693672553, 1.5229507040072823, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(289992, 'HP:0031094', 'Abnormal breast physiology', 'XPO:0141719', 'abnormal anterior notochord morphology', 0.47619047619047616, 4.638757693672553, 1.4862477031377266, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(289993, 'HP:0031094', 'Abnormal breast physiology', 'XPO:0140559', 'abnormally necrotic articular system', 0.43478260869565216, 4.638757693672553, 1.4201588541997616, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(289994, 'HP:0031094', 'Abnormal breast physiology', 'XPO:0102130', 'abnormal endoskeleton morphology', 0.4444444444444444, 4.638757693672553, 1.4358516936218344, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(289995, 'HP:0031094', 'Abnormal breast physiology', 'XPO:0141713', 'increased size of the posterior notochord', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(289996, 'HP:0031094', 'Abnormal breast physiology', 'XPO:0140043', 'abnormally necrotic perichondrium', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(289997, 'HP:0031094', 'Abnormal breast physiology', 'XPO:0141708', 'decreased size of the posterior notochord', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(289998, 'HP:0031094', 'Abnormal breast physiology', 'XPO:0102567', 'abnormal skeleton morphology', 0.47619047619047616, 4.638757693672553, 1.4862477031377266, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(289999, 'HP:0031094', 'Abnormal breast physiology', 'XPO:0102217', 'abnormal elastica externa morphology', 0.5, 4.638757693672553, 1.5229507040072823, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(290000, 'HP:0031094', 'Abnormal breast physiology', 'XPO:0102272', 'abnormal notochordal sheath morphology', 0.47619047619047616, 4.638757693672553, 1.4862477031377266, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(290001, 'HP:0031094', 'Abnormal breast physiology', 'XPO:0102093', 'abnormal craniofacial skeleton morphology', 0.4375, 6.211345574613551, 1.6484731386629958, 'UPHENO:0087089', 'abnormal axial skeleton plus cranial skeleton morphology'),
(290002, 'HP:0031094', 'Abnormal breast physiology', 'XPO:0129786', 'increased size of the articular system', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(290003, 'HP:0031094', 'Abnormal breast physiology', 'XPO:0101713', 'abnormal anatomical entity in vitro morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(290004, 'HP:0031094', 'Abnormal breast physiology', 'XPO:0102828', 'abnormal occipital region morphology', 0.4107142857142857, 6.272837960958401, 1.6050994245019483, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(290005, 'HP:0031094', 'Abnormal breast physiology', 'XPO:0100226', 'abnormal vertebral element', 0.46, 6.272837960958401, 1.69867756270602, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(290006, 'HP:0031094', 'Abnormal breast physiology', 'XPO:0140432', 'abnormally necrotic skeleton', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(290007, 'HP:0031094', 'Abnormal breast physiology', 'XPO:0128709', 'decreased size of the flexural organ', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(290008, 'HP:0031094', 'Abnormal breast physiology', 'XPO:0128306', 'decreased size of the articular system', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(290009, 'HP:0031094', 'Abnormal breast physiology', 'XPO:0103152', 'abnormal otic region morphology', 0.40350877192982454, 6.272837960958401, 1.5909573036826314, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(290010, 'HP:0031094', 'Abnormal breast physiology', 'XPO:0102144', 'abnormal cranial skeleton morphology', 0.45652173913043476, 6.211345574613551, 1.6839282300806968, 'UPHENO:0087089', 'abnormal axial skeleton plus cranial skeleton morphology'),
(290011, 'HP:0031094', 'Abnormal breast physiology', 'XPO:0102806', 'abnormal articular system morphology', 0.4878048780487805, 4.638757693672553, 1.5042634845863214, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(290012, 'HP:0031094', 'Abnormal breast physiology', 'XPO:0101860', 'abnormal skeletal subdivision morphology', 0.46511627906976744, 4.638757693672553, 1.4688640910537754, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(290013, 'HP:0031094', 'Abnormal breast physiology', 'XPO:0102514', 'abnormal perichondrial cell morphology', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(290014, 'HP:0031094', 'Abnormal breast physiology', 'XPO:0139998', 'abnormally necrotic axial skeleton', 0.4117647058823529, 6.211345574613551, 1.599253852164941, 'UPHENO:0087089', 'abnormal axial skeleton plus cranial skeleton morphology'),
(290015, 'HP:0031094', 'Abnormal breast physiology', 'XPO:0101982', 'abnormal appendicular skeleton morphology', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(290016, 'HP:0031094', 'Abnormal breast physiology', 'XPO:0139917', 'abnormally necrotic notochord', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(290017, 'HP:0031094', 'Abnormal breast physiology', 'XPO:0102351', 'abnormal sphenoid region morphology', 0.40350877192982454, 6.272837960958401, 1.5909573036826314, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(290018, 'HP:0031094', 'Abnormal breast physiology', 'XPO:0128352', 'decreased size of the skeletal system', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(290019, 'HP:0031094', 'Abnormal breast physiology', 'XPO:0102113', 'abnormal anatomical line morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(290020, 'HP:0031094', 'Abnormal breast physiology', 'XPO:0100693', 'abnormal vertebral centrum', 0.45098039215686275, 6.272837960958401, 1.6819414150229712, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(290021, 'HP:0031094', 'Abnormal breast physiology', 'XPO:0107372', 'abnormal flexural organ morphology', 0.47619047619047616, 4.638757693672553, 1.4862477031377266, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(290022, 'HP:0031094', 'Abnormal breast physiology', 'XPO:0139774', 'abnormally necrotic elastica externa', 0.4444444444444444, 4.638757693672553, 1.4358516936218344, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(290023, 'HP:0031094', 'Abnormal breast physiology', 'XPO:0141703', 'abnormally necrotic posterior notochord', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(290024, 'HP:0031094', 'Abnormal breast physiology', 'XPO:0129832', 'increased size of the skeletal system', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(290025, 'HP:0031094', 'Abnormal breast physiology', 'XPO:0101976', 'abnormal portion of organism substance morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(290026, 'HP:0031094', 'Abnormal breast physiology', 'XPO:0139889', 'abnormally necrotic cranial skeleton', 0.40384615384615385, 6.211345574613551, 1.5838017617482976, 'UPHENO:0087089', 'abnormal axial skeleton plus cranial skeleton morphology'),
(290027, 'HP:0031094', 'Abnormal breast physiology', 'XPO:0141699', 'abnormally necrotic anterior notochord', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(290028, 'HP:0031094', 'Abnormal breast physiology', 'XPO:0102216', 'abnormal vertebral column morphology', 0.46, 6.272837960958401, 1.69867756270602, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(290029, 'HP:0031094', 'Abnormal breast physiology', 'XPO:0102010', 'abnormal perichondrium morphology', 0.46511627906976744, 4.638757693672553, 1.4688640910537754, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(290030, 'HP:0031094', 'Abnormal breast physiology', 'XPO:0130060', 'increased size of the postcranial axial skeleton', 0.42592592592592593, 6.272837960958401, 1.6345532468244968, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(290031, 'HP:0031094', 'Abnormal breast physiology', 'XPO:0128184', 'decreased size of the skeleton', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(290032, 'HP:0031094', 'Abnormal breast physiology', 'XPO:0128580', 'decreased size of the postcranial axial skeleton', 0.42592592592592593, 6.272837960958401, 1.6345532468244968, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(290033, 'HP:0031094', 'Abnormal breast physiology', 'XPO:0130368', 'increased size of the elastica externa', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(290034, 'HP:0031094', 'Abnormal breast physiology', 'XPO:0139771', 'abnormally necrotic skeletal subdivision', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(290035, 'HP:0031094', 'Abnormal breast physiology', 'XPO:0141723', 'abnormal posterior notochord morphology', 0.47619047619047616, 4.638757693672553, 1.4862477031377266, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(290036, 'HP:0031094', 'Abnormal breast physiology', 'XPO:0140683', 'abnormally necrotic flexural organ', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(290037, 'HP:0031094', 'Abnormal breast physiology', 'XPO:0130188', 'increased size of the flexural organ', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(290038, 'HP:0031094', 'Abnormal breast physiology', 'XPO:0102728', 'abnormal tendon morphology', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(290039, 'HP:0031094', 'Abnormal breast physiology', 'XPO:0101680', 'abnormal skeletal element morphology', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(290040, 'HP:0031094', 'Abnormal breast physiology', 'XPO:0101638', 'abnormal anatomical structure morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(290041, 'HP:0031094', 'Abnormal breast physiology', 'XPO:0102461', 'abnormal postcranial axial skeleton morphology', 0.5, 6.272837960958401, 1.770993783297728, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(290042, 'HP:0031094', 'Abnormal breast physiology', 'XPO:0126886', 'abnormally localised vertebral column', 0.4339622641509434, 6.272837960958401, 1.6499015013598524, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(290043, 'HP:0031094', 'Abnormal breast physiology', 'XPO:0141704', 'decreased size of the anterior notochord', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(290044, 'HP:0031094', 'Abnormal breast physiology', 'XPO:0129434', 'decreased size of the notochordal sheath', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(290045, 'HP:0031094', 'Abnormal breast physiology', 'XPO:0140510', 'abnormally necrotic postcranial axial skeleton', 0.4423076923076923, 6.272837960958401, 1.6656903922192745, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(290046, 'HP:0031094', 'Abnormal breast physiology', 'XPO:0100584', 'abnormal vertebral column', 0.5227272727272727, 6.272837960958401, 1.810796366130629, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(290047, 'HP:0031094', 'Abnormal breast physiology', 'XPO:0102542', 'abnormal vacuolated notochordal tissue morphology', 0.43478260869565216, 4.638757693672553, 1.4201588541997616, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(290048, 'HP:0031094', 'Abnormal breast physiology', 'XPO:0102054', 'abnormal notochord morphology', 0.47619047619047616, 4.638757693672553, 1.4862477031377266, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(290049, 'HP:0031094', 'Abnormal breast physiology', 'XPO:0101957', 'abnormal axial skeleton morphology', 0.4666666666666667, 6.211345574613551, 1.702535736723214, 'UPHENO:0087089', 'abnormal axial skeleton plus cranial skeleton morphology'),
(290050, 'HP:0031094', 'Abnormal breast physiology', 'XPO:0125260', 'absent vertebral column', 0.4107142857142857, 6.272837960958401, 1.6050994245019483, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(290051, 'HP:0031094', 'Abnormal breast physiology', 'XPO:0130908', 'increased size of the notochordal sheath', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(290052, 'HP:0031094', 'Abnormal breast physiology', 'XPO:0102605', 'abnormal dermal skeleton morphology', 0.4444444444444444, 4.638757693672553, 1.4358516936218344, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(290053, 'HP:0031094', 'Abnormal breast physiology', 'XPO:0102564', 'abnormal olfactory region morphology', 0.40350877192982454, 6.272837960958401, 1.5909573036826314, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(290054, 'HP:0031094', 'Abnormal breast physiology', 'XPO:0102164', 'abnormal mandibular mesenchyme morphology', 0.4117647058823529, 6.211345574613551, 1.599253852164941, 'UPHENO:0087089', 'abnormal axial skeleton plus cranial skeleton morphology'),
(290055, 'HP:0031094', 'Abnormal breast physiology', 'XPO:0103116', 'abnormal bone marrow morphology', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(290056, 'HP:0031094', 'Abnormal breast physiology', 'XPO:0140103', 'abnormally necrotic vertebral column', 0.4107142857142857, 6.272837960958401, 1.6050994245019483, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(290057, 'HP:0031094', 'Abnormal breast physiology', 'XPO:0128890', 'decreased size of the elastica externa', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(290058, 'HP:0031094', 'Abnormal breast physiology', 'XPO:0103218', 'abnormal joint morphology', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(290059, 'HP:0033523', 'Abnormal sperm principal piece morphology', 'XPO:0102648', 'abnormal egg morphology', 0.47058823529411764, 6.723205497167461, 1.7787246584088685, 'UPHENO:0087547', 'abnormal reproductive system morphology'),
(290060, 'HP:0033523', 'Abnormal sperm principal piece morphology', 'XPO:0140723', 'abnormally necrotic polar body', 0.5714285714285714, 10.532569744119352, 2.453285813425316, 'HP:0012862', 'Abnormal germ cell morphology'),
(290061, 'HP:0033523', 'Abnormal sperm principal piece morphology', 'XPO:0140803', 'abnormally necrotic pericyte', 0.40425531914893614, 5.43643956286526, 1.4824674062251753, 'HP:0025461', 'Abnormal cell morphology'),
(290062, 'HP:0033523', 'Abnormal sperm principal piece morphology', 'XPO:0102636', 'abnormal acid secreting cell morphology', 0.4418604651162791, 5.43643956286526, 1.5498863551319448, 'HP:0025461', 'Abnormal cell morphology'),
(290063, 'HP:0033523', 'Abnormal sperm principal piece morphology', 'XPO:0141147', 'abnormally necrotic alkali secreting cell', 0.40425531914893614, 5.43643956286526, 1.4824674062251753, 'HP:0025461', 'Abnormal cell morphology'),
(290064, 'HP:0033523', 'Abnormal sperm principal piece morphology', 'XPO:0140496', 'abnormally necrotic egg', 0.42105263157894735, 6.723205497167461, 1.6825050868358185, 'UPHENO:0087547', 'abnormal reproductive system morphology'),
(290065, 'HP:0033523', 'Abnormal sperm principal piece morphology', 'XPO:0141065', 'abnormally necrotic paracrine cell', 0.40425531914893614, 5.43643956286526, 1.4824674062251753, 'HP:0025461', 'Abnormal cell morphology'),
(290066, 'HP:0033523', 'Abnormal sperm principal piece morphology', 'XPO:0140868', 'abnormally necrotic chondroblast', 0.40425531914893614, 5.43643956286526, 1.4824674062251753, 'HP:0025461', 'Abnormal cell morphology'),
(290067, 'HP:0033523', 'Abnormal sperm principal piece morphology', 'XPO:0103130', 'abnormal stage II oocyte morphology', 0.40425531914893614, 5.43643956286526, 1.4824674062251753, 'HP:0025461', 'Abnormal cell morphology'),
(290068, 'HP:0033523', 'Abnormal sperm principal piece morphology', 'XPO:0101636', 'abnormal cell morphology', 0.4634146341463415, 5.43643956286526, 1.587238372483447, 'HP:0025461', 'Abnormal cell morphology'),
(290069, 'HP:0033523', 'Abnormal sperm principal piece morphology', 'XPO:0130929', 'increased size of the polar body', 0.49122807017543857, 10.532569744119352, 2.2746195087073273, 'HP:0012862', 'Abnormal germ cell morphology'),
(290070, 'HP:0033523', 'Abnormal sperm principal piece morphology', 'XPO:0101740', 'abnormal cell part morphology', 0.40476190476190477, 3.6715585125471644, 1.219059890646631, 'UPHENO:0086172', 'abnormal cell'),
(290071, 'HP:0033523', 'Abnormal sperm principal piece morphology', 'XPO:0101921', 'abnormal chondroblast morphology', 0.4418604651162791, 5.43643956286526, 1.5498863551319448, 'HP:0025461', 'Abnormal cell morphology'),
(290072, 'HP:0033523', 'Abnormal sperm principal piece morphology', 'XPO:0103005', 'abnormal oxygen accumulating cell morphology', 0.4418604651162791, 5.43643956286526, 1.5498863551319448, 'HP:0025461', 'Abnormal cell morphology'),
(290073, 'HP:0033523', 'Abnormal sperm principal piece morphology', 'XPO:0139717', 'abnormally necrotic cell', 0.4318181818181818, 5.43643956286526, 1.532172786470543, 'HP:0025461', 'Abnormal cell morphology'),
(290074, 'HP:0033523', 'Abnormal sperm principal piece morphology', 'XPO:0101940', 'abnormal early embryonic cell morphology', 0.4222222222222222, 5.43643956286526, 1.5150530001322648, 'HP:0025461', 'Abnormal cell morphology'),
(290075, 'HP:0033523', 'Abnormal sperm principal piece morphology', 'XPO:0102864', 'abnormal female genitalia morphology', 0.4230769230769231, 7.005035523447265, 1.7215309684419309, 'HP:0012243', 'Abnormal reproductive system morphology'),
(290076, 'HP:0033523', 'Abnormal sperm principal piece morphology', 'XPO:0102965', 'abnormal barrier epithelial cell morphology', 0.4418604651162791, 5.43643956286526, 1.5498863551319448, 'HP:0025461', 'Abnormal cell morphology'),
(290077, 'HP:0033523', 'Abnormal sperm principal piece morphology', 'XPO:0101657', 'abnormal oocyte morphology', 0.4222222222222222, 5.43643956286526, 1.5150530001322648, 'HP:0025461', 'Abnormal cell morphology'),
(290078, 'HP:0033523', 'Abnormal sperm principal piece morphology', 'XPO:0103100', 'abnormal stage I oocyte morphology', 0.40425531914893614, 5.43643956286526, 1.4824674062251753, 'HP:0025461', 'Abnormal cell morphology'),
(290079, 'HP:0033523', 'Abnormal sperm principal piece morphology', 'XPO:0140600', 'abnormally necrotic apoptotic cell', 0.40425531914893614, 5.43643956286526, 1.4824674062251753, 'HP:0025461', 'Abnormal cell morphology'),
(290080, 'HP:0033523', 'Abnormal sperm principal piece morphology', 'XPO:0140068', 'abnormally necrotic myoblast', 0.40425531914893614, 5.43643956286526, 1.4824674062251753, 'HP:0025461', 'Abnormal cell morphology'),
(290081, 'HP:0033523', 'Abnormal sperm principal piece morphology', 'XPO:0102531', 'abnormal secondary spermatogonium morphology', 0.4222222222222222, 5.43643956286526, 1.5150530001322648, 'HP:0025461', 'Abnormal cell morphology'),
(290082, 'HP:0033523', 'Abnormal sperm principal piece morphology', 'XPO:0140278', 'abnormally necrotic Merkel cell', 0.40425531914893614, 5.43643956286526, 1.4824674062251753, 'HP:0025461', 'Abnormal cell morphology'),
(290083, 'HP:0033523', 'Abnormal sperm principal piece morphology', 'XPO:0102109', 'abnormal pericyte morphology', 0.4418604651162791, 5.43643956286526, 1.5498863551319448, 'HP:0025461', 'Abnormal cell morphology'),
(290084, 'HP:0033523', 'Abnormal sperm principal piece morphology', 'XPO:0140647', 'abnormally necrotic nucleate erythrocyte', 0.40425531914893614, 5.43643956286526, 1.4824674062251753, 'HP:0025461', 'Abnormal cell morphology'),
(290085, 'HP:0033523', 'Abnormal sperm principal piece morphology', 'XPO:0102764', 'abnormal apoptotic cell morphology', 0.4418604651162791, 5.43643956286526, 1.5498863551319448, 'HP:0025461', 'Abnormal cell morphology'),
(290086, 'HP:0033523', 'Abnormal sperm principal piece morphology', 'XPO:0102860', 'abnormal mesenchymal stem cell morphology', 0.4222222222222222, 5.43643956286526, 1.5150530001322648, 'HP:0025461', 'Abnormal cell morphology'),
(290087, 'HP:0033523', 'Abnormal sperm principal piece morphology', 'XPO:0102397', 'abnormal male genitalia morphology', 0.4230769230769231, 7.005035523447265, 1.7215309684419309, 'UPHENO:0020950', 'abnormal reproductive system morphology'),
(290088, 'HP:0033523', 'Abnormal sperm principal piece morphology', 'XPO:0102608', 'abnormal multiciliated cell morphology', 0.4222222222222222, 5.43643956286526, 1.5150530001322648, 'HP:0025461', 'Abnormal cell morphology'),
(290089, 'HP:0033523', 'Abnormal sperm principal piece morphology', 'XPO:0101232', 'abnormal female genitalia', 0.4782608695652174, 7.005035523447265, 1.8303645486020337, 'UPHENO:0020950', 'abnormal reproductive system morphology'),
(290090, 'HP:0033523', 'Abnormal sperm principal piece morphology', 'XPO:0129864', 'increased size of the genital system', 0.41509433962264153, 7.005035523447265, 1.705212771075354, 'HP:0012243', 'Abnormal reproductive system morphology'),
(290091, 'HP:0033523', 'Abnormal sperm principal piece morphology', 'XPO:0102165', 'abnormal melanoblast morphology', 0.4418604651162791, 5.43643956286526, 1.5498863551319448, 'HP:0025461', 'Abnormal cell morphology'),
(290092, 'HP:0033523', 'Abnormal sperm principal piece morphology', 'XPO:0129455', 'decreased size of the polar body', 0.49122807017543857, 10.532569744119352, 2.2746195087073273, 'HP:0012862', 'Abnormal germ cell morphology'),
(290093, 'HP:0033523', 'Abnormal sperm principal piece morphology', 'XPO:0141007', 'abnormally necrotic electrically active cell', 0.40425531914893614, 5.43643956286526, 1.4824674062251753, 'HP:0025461', 'Abnormal cell morphology'),
(290094, 'HP:0033523', 'Abnormal sperm principal piece morphology', 'XPO:0140919', 'abnormally necrotic cementoblast', 0.40425531914893614, 5.43643956286526, 1.4824674062251753, 'HP:0025461', 'Abnormal cell morphology'),
(290095, 'HP:0033523', 'Abnormal sperm principal piece morphology', 'XPO:0102258', 'abnormal primordial germ cell morphology', 0.4222222222222222, 5.43643956286526, 1.5150530001322648, 'HP:0025461', 'Abnormal cell morphology'),
(290096, 'HP:0033523', 'Abnormal sperm principal piece morphology', 'XPO:0102873', 'abnormal nucleate erythrocyte morphology', 0.4418604651162791, 5.43643956286526, 1.5498863551319448, 'HP:0025461', 'Abnormal cell morphology'),
(290097, 'HP:0033523', 'Abnormal sperm principal piece morphology', 'XPO:0101658', 'abnormal germ cell morphology', 0.4418604651162791, 5.43643956286526, 1.5498863551319448, 'HP:0025461', 'Abnormal cell morphology'),
(290098, 'HP:0033523', 'Abnormal sperm principal piece morphology', 'XPO:0140381', 'abnormally necrotic ciliated cell', 0.40425531914893614, 5.43643956286526, 1.4824674062251753, 'HP:0025461', 'Abnormal cell morphology'),
(290099, 'HP:0033523', 'Abnormal sperm principal piece morphology', 'XPO:0103167', 'abnormal absorptive cell morphology', 0.4418604651162791, 5.43643956286526, 1.5498863551319448, 'HP:0025461', 'Abnormal cell morphology'),
(290100, 'HP:0033523', 'Abnormal sperm principal piece morphology', 'XPO:0141154', 'abnormally necrotic barrier cell', 0.40425531914893614, 5.43643956286526, 1.4824674062251753, 'HP:0025461', 'Abnormal cell morphology'),
(290101, 'HP:0033523', 'Abnormal sperm principal piece morphology', 'XPO:0102929', 'abnormal barrier cell morphology', 0.4418604651162791, 5.43643956286526, 1.5498863551319448, 'HP:0025461', 'Abnormal cell morphology'),
(290102, 'HP:0033523', 'Abnormal sperm principal piece morphology', 'XPO:0140899', 'abnormally necrotic mucus secreting cell', 0.40425531914893614, 5.43643956286526, 1.4824674062251753, 'HP:0025461', 'Abnormal cell morphology'),
(290103, 'HP:0033523', 'Abnormal sperm principal piece morphology', 'XPO:0128384', 'decreased size of the genital system', 0.41509433962264153, 7.005035523447265, 1.705212771075354, 'HP:0012243', 'Abnormal reproductive system morphology'),
(290104, 'HP:0033523', 'Abnormal sperm principal piece morphology', 'XPO:0140471', 'abnormally necrotic multiciliated cell precursor', 0.40425531914893614, 5.43643956286526, 1.4824674062251753, 'HP:0025461', 'Abnormal cell morphology'),
(290105, 'HP:0033523', 'Abnormal sperm principal piece morphology', 'XPO:0102745', 'abnormal stage IV oocyte morphology', 0.40425531914893614, 5.43643956286526, 1.4824674062251753, 'HP:0025461', 'Abnormal cell morphology'),
(290106, 'HP:0033523', 'Abnormal sperm principal piece morphology', 'XPO:0102181', 'abnormal mitotic cell morphology', 0.4418604651162791, 5.43643956286526, 1.5498863551319448, 'HP:0025461', 'Abnormal cell morphology'),
(290107, 'HP:0033523', 'Abnormal sperm principal piece morphology', 'XPO:0101850', 'abnormal epithelial cell morphology', 0.41304347826086957, 5.43643956286526, 1.4984945466703803, 'HP:0025461', 'Abnormal cell morphology'),
(290108, 'HP:0033523', 'Abnormal sperm principal piece morphology', 'XPO:0103099', 'abnormal alkali secreting cell morphology', 0.4418604651162791, 5.43643956286526, 1.5498863551319448, 'HP:0025461', 'Abnormal cell morphology'),
(290109, 'HP:0033523', 'Abnormal sperm principal piece morphology', 'XPO:0140239', 'abnormally necrotic absorptive cell', 0.40425531914893614, 5.43643956286526, 1.4824674062251753, 'HP:0025461', 'Abnormal cell morphology'),
(290110, 'HP:0033523', 'Abnormal sperm principal piece morphology', 'XPO:0102549', 'abnormal stage III oocyte morphology', 0.40425531914893614, 5.43643956286526, 1.4824674062251753, 'HP:0025461', 'Abnormal cell morphology'),
(290111, 'HP:0033523', 'Abnormal sperm principal piece morphology', 'XPO:0101752', 'abnormal genital system morphology', 0.4782608695652174, 7.005035523447265, 1.8303645486020337, 'UPHENO:0020950', 'abnormal reproductive system morphology'),
(290112, 'HP:0033523', 'Abnormal sperm principal piece morphology', 'XPO:0102285', 'abnormal myoblast morphology', 0.4418604651162791, 5.43643956286526, 1.5498863551319448, 'HP:0025461', 'Abnormal cell morphology'),
(290113, 'HP:0033523', 'Abnormal sperm principal piece morphology', 'XPO:0140075', 'abnormally necrotic stem cell', 0.40425531914893614, 5.43643956286526, 1.4824674062251753, 'HP:0025461', 'Abnormal cell morphology'),
(290114, 'HP:0033523', 'Abnormal sperm principal piece morphology', 'XPO:0101804', 'abnormal stem cell morphology', 0.4418604651162791, 5.43643956286526, 1.5498863551319448, 'HP:0025461', 'Abnormal cell morphology'),
(290115, 'HP:0033523', 'Abnormal sperm principal piece morphology', 'XPO:0140533', 'abnormally necrotic myelin accumulating cell', 0.40425531914893614, 5.43643956286526, 1.4824674062251753, 'HP:0025461', 'Abnormal cell morphology'),
(290116, 'HP:0033523', 'Abnormal sperm principal piece morphology', 'XPO:0139867', 'abnormally necrotic genital system', 0.43137254901960786, 7.005035523447265, 1.7383267902561792, 'UPHENO:0020950', 'abnormal reproductive system morphology'),
(290117, 'HP:0033523', 'Abnormal sperm principal piece morphology', 'XPO:0140010', 'abnormally necrotic zygote', 0.40425531914893614, 5.43643956286526, 1.4824674062251753, 'HP:0025461', 'Abnormal cell morphology'),
(290118, 'HP:0033523', 'Abnormal sperm principal piece morphology', 'XPO:0101969', 'abnormal zygote morphology', 0.4418604651162791, 5.43643956286526, 1.5498863551319448, 'HP:0025461', 'Abnormal cell morphology'),
(290119, 'HP:0033523', 'Abnormal sperm principal piece morphology', 'XPO:0102306', 'abnormal secondary oogonium morphology', 0.4222222222222222, 5.43643956286526, 1.5150530001322648, 'HP:0025461', 'Abnormal cell morphology'),
(290120, 'HP:0033523', 'Abnormal sperm principal piece morphology', 'XPO:0101939', 'abnormal blastomere morphology', 0.40425531914893614, 5.43643956286526, 1.4824674062251753, 'HP:0025461', 'Abnormal cell morphology'),
(290121, 'HP:0033523', 'Abnormal sperm principal piece morphology', 'XPO:0140752', 'abnormally necrotic melanoblast', 0.40425531914893614, 5.43643956286526, 1.4824674062251753, 'HP:0025461', 'Abnormal cell morphology'),
(290122, 'HP:0033523', 'Abnormal sperm principal piece morphology', 'XPO:0140760', 'abnormally necrotic spermatozoon', 0.42105263157894735, 6.723205497167461, 1.6825050868358185, 'UPHENO:0087547', 'abnormal reproductive system morphology'),
(290123, 'HP:0033523', 'Abnormal sperm principal piece morphology', 'XPO:0102958', 'abnormal cementoblast morphology', 0.4418604651162791, 5.43643956286526, 1.5498863551319448, 'HP:0025461', 'Abnormal cell morphology'),
(290124, 'HP:0033523', 'Abnormal sperm principal piece morphology', 'XPO:0102386', 'abnormal electrically active cell morphology', 0.4418604651162791, 5.43643956286526, 1.5498863551319448, 'HP:0025461', 'Abnormal cell morphology'),
(290125, 'HP:0033523', 'Abnormal sperm principal piece morphology', 'XPO:0102147', 'abnormal somatic stem cell morphology', 0.4222222222222222, 5.43643956286526, 1.5150530001322648, 'HP:0025461', 'Abnormal cell morphology'),
(290126, 'HP:0033523', 'Abnormal sperm principal piece morphology', 'XPO:0141203', 'abnormally necrotic exocrine cell', 0.40425531914893614, 5.43643956286526, 1.4824674062251753, 'HP:0025461', 'Abnormal cell morphology'),
(290127, 'HP:0033523', 'Abnormal sperm principal piece morphology', 'XPO:0103067', 'abnormal paracrine cell morphology', 0.4418604651162791, 5.43643956286526, 1.5498863551319448, 'HP:0025461', 'Abnormal cell morphology'),
(290128, 'HP:0033523', 'Abnormal sperm principal piece morphology', 'XPO:0102336', 'abnormal Merkel cell morphology', 0.4418604651162791, 5.43643956286526, 1.5498863551319448, 'HP:0025461', 'Abnormal cell morphology'),
(290129, 'HP:0033523', 'Abnormal sperm principal piece morphology', 'XPO:0140589', 'abnormally necrotic keratin accumulating cell', 0.40425531914893614, 5.43643956286526, 1.4824674062251753, 'HP:0025461', 'Abnormal cell morphology'),
(290130, 'HP:0033523', 'Abnormal sperm principal piece morphology', 'XPO:0102061', 'abnormal spermatid morphology', 0.4222222222222222, 5.43643956286526, 1.5150530001322648, 'HP:0025461', 'Abnormal cell morphology'),
(290131, 'HP:0033523', 'Abnormal sperm principal piece morphology', 'XPO:0139929', 'abnormally necrotic barrier epithelial cell', 0.40425531914893614, 5.43643956286526, 1.4824674062251753, 'HP:0025461', 'Abnormal cell morphology'),
(290132, 'HP:0033523', 'Abnormal sperm principal piece morphology', 'XPO:0101808', 'abnormal stage VI oocyte morphology', 0.40425531914893614, 5.43643956286526, 1.4824674062251753, 'HP:0025461', 'Abnormal cell morphology'),
(290133, 'HP:0033523', 'Abnormal sperm principal piece morphology', 'XPO:0100765', 'abnormal male genitalia', 0.4782608695652174, 7.005035523447265, 1.8303645486020337, 'HP:0012243', 'Abnormal reproductive system morphology'),
(290134, 'HP:0033523', 'Abnormal sperm principal piece morphology', 'XPO:0101948', 'abnormal gamete morphology', 0.4897959183673469, 6.723205497167461, 1.8146621203016091, 'UPHENO:0087547', 'abnormal reproductive system morphology'),
(290135, 'HP:0033523', 'Abnormal sperm principal piece morphology', 'XPO:0139839', 'abnormally necrotic progenitor cell', 0.40425531914893614, 5.43643956286526, 1.4824674062251753, 'HP:0025461', 'Abnormal cell morphology'),
(290136, 'HP:0033523', 'Abnormal sperm principal piece morphology', 'XPO:0139992', 'abnormally necrotic gamete', 0.4444444444444444, 6.723205497167461, 1.7286096528928754, 'UPHENO:0087547', 'abnormal reproductive system morphology'),
(290137, 'HP:0033523', 'Abnormal sperm principal piece morphology', 'XPO:0102270', 'abnormal polar body morphology', 0.6222222222222222, 10.532569744119352, 2.559999795292274, 'HP:0012862', 'Abnormal germ cell morphology'),
(290138, 'HP:0033523', 'Abnormal sperm principal piece morphology', 'XPO:0101917', 'abnormal progenitor cell morphology', 0.4418604651162791, 5.43643956286526, 1.5498863551319448, 'HP:0025461', 'Abnormal cell morphology'),
(290139, 'HP:0033523', 'Abnormal sperm principal piece morphology', 'XPO:0141048', 'abnormally necrotic mitotic cell', 0.40425531914893614, 5.43643956286526, 1.4824674062251753, 'HP:0025461', 'Abnormal cell morphology'),
(290140, 'HP:0033523', 'Abnormal sperm principal piece morphology', 'XPO:0107371', 'abnormal migrating myoblast morphology', 0.4222222222222222, 5.43643956286526, 1.5150530001322648, 'HP:0025461', 'Abnormal cell morphology'),
(290141, 'HP:0033523', 'Abnormal sperm principal piece morphology', 'XPO:0103112', 'abnormal stage V oocyte morphology', 0.40425531914893614, 5.43643956286526, 1.4824674062251753, 'HP:0025461', 'Abnormal cell morphology'),
(290142, 'HP:0033523', 'Abnormal sperm principal piece morphology', 'XPO:0102869', 'abnormal mucus secreting cell morphology', 0.4418604651162791, 5.43643956286526, 1.5498863551319448, 'HP:0025461', 'Abnormal cell morphology'),
(290143, 'HP:0033523', 'Abnormal sperm principal piece morphology', 'XPO:0102347', 'abnormal ciliated cell morphology', 0.4418604651162791, 5.43643956286526, 1.5498863551319448, 'HP:0025461', 'Abnormal cell morphology'),
(290144, 'HP:0033523', 'Abnormal sperm principal piece morphology', 'XPO:0102434', 'abnormal exocrine cell morphology', 0.4418604651162791, 5.43643956286526, 1.5498863551319448, 'HP:0025461', 'Abnormal cell morphology'),
(290145, 'HP:0033523', 'Abnormal sperm principal piece morphology', 'XPO:0101262', 'abnormal oviduct', 0.44, 7.005035523447265, 1.755624000267938, 'UPHENO:0020950', 'abnormal reproductive system morphology'),
(290146, 'HP:0033523', 'Abnormal sperm principal piece morphology', 'XPO:0102998', 'abnormal morula cell morphology', 0.40425531914893614, 5.43643956286526, 1.4824674062251753, 'HP:0025461', 'Abnormal cell morphology'),
(290147, 'HP:0033523', 'Abnormal sperm principal piece morphology', 'XPO:0141146', 'abnormally necrotic oxygen accumulating cell', 0.40425531914893614, 5.43643956286526, 1.4824674062251753, 'HP:0025461', 'Abnormal cell morphology'),
(290148, 'HP:0033523', 'Abnormal sperm principal piece morphology', 'XPO:0102206', 'abnormal gastrula cell morphology', 0.40425531914893614, 5.43643956286526, 1.4824674062251753, 'HP:0025461', 'Abnormal cell morphology'),
(290149, 'HP:0033523', 'Abnormal sperm principal piece morphology', 'XPO:0102872', 'abnormal ciliated non-epidermal cell morphology', 0.4222222222222222, 5.43643956286526, 1.5150530001322648, 'HP:0025461', 'Abnormal cell morphology'),
(290150, 'HP:0033523', 'Abnormal sperm principal piece morphology', 'XPO:0102556', 'abnormal spermatozoon morphology', 0.47058823529411764, 6.723205497167461, 1.7787246584088685, 'UPHENO:0087547', 'abnormal reproductive system morphology'),
(290151, 'HP:0033523', 'Abnormal sperm principal piece morphology', 'XPO:0102423', 'abnormal multiciliated cell precursor morphology', 0.4418604651162791, 5.43643956286526, 1.5498863551319448, 'HP:0025461', 'Abnormal cell morphology'),
(290152, 'HP:0033523', 'Abnormal sperm principal piece morphology', 'XPO:0139759', 'abnormally necrotic germ cell', 0.40425531914893614, 5.43643956286526, 1.4824674062251753, 'HP:0025461', 'Abnormal cell morphology'),
(290153, 'HP:0033523', 'Abnormal sperm principal piece morphology', 'XPO:0103080', 'abnormal myelin accumulating cell morphology', 0.4418604651162791, 5.43643956286526, 1.5498863551319448, 'HP:0025461', 'Abnormal cell morphology'),
(290154, 'HP:0033523', 'Abnormal sperm principal piece morphology', 'XPO:0102534', 'abnormal spermatocyte morphology', 0.4222222222222222, 5.43643956286526, 1.5150530001322648, 'HP:0025461', 'Abnormal cell morphology'),
(290155, 'HP:0033523', 'Abnormal sperm principal piece morphology', 'XPO:0102069', 'abnormal proepicardium morphology', 0.4222222222222222, 5.43643956286526, 1.5150530001322648, 'HP:0025461', 'Abnormal cell morphology'),
(290156, 'HP:0033523', 'Abnormal sperm principal piece morphology', 'XPO:0102323', 'abnormal keratin accumulating cell morphology', 0.4418604651162791, 5.43643956286526, 1.5498863551319448, 'HP:0025461', 'Abnormal cell morphology'),
(290157, 'HP:0033523', 'Abnormal sperm principal piece morphology', 'XPO:0100666', 'abnormal primary spermatogonium', 0.4067796610169492, 7.005035523447265, 1.6880479778843864, 'HP:0012243', 'Abnormal reproductive system morphology'),
(290158, 'HP:0033523', 'Abnormal sperm principal piece morphology', 'XPO:0140709', 'abnormally necrotic acid secreting cell', 0.40425531914893614, 5.43643956286526, 1.4824674062251753, 'HP:0025461', 'Abnormal cell morphology'),
(290159, 'HP:0034947', 'Altered location of the longitudinal column in the fibrous sheath', 'XPO:0102347', 'abnormal ciliated cell morphology', 0.4418604651162791, 5.43643956286526, 1.5498863551319448, 'HP:0025461', 'Abnormal cell morphology'),
(290160, 'HP:0034947', 'Altered location of the longitudinal column in the fibrous sheath', 'XPO:0102061', 'abnormal spermatid morphology', 0.4222222222222222, 5.43643956286526, 1.5150530001322648, 'HP:0025461', 'Abnormal cell morphology'),
(290161, 'HP:0034947', 'Altered location of the longitudinal column in the fibrous sheath', 'XPO:0129864', 'increased size of the genital system', 0.41509433962264153, 7.005035523447265, 1.705212771075354, 'UPHENO:0020950', 'abnormal reproductive system morphology'),
(290162, 'HP:0034947', 'Altered location of the longitudinal column in the fibrous sheath', 'XPO:0140589', 'abnormally necrotic keratin accumulating cell', 0.40425531914893614, 5.43643956286526, 1.4824674062251753, 'HP:0025461', 'Abnormal cell morphology'),
(290163, 'HP:0034947', 'Altered location of the longitudinal column in the fibrous sheath', 'XPO:0140278', 'abnormally necrotic Merkel cell', 0.40425531914893614, 5.43643956286526, 1.4824674062251753, 'HP:0025461', 'Abnormal cell morphology'),
(290164, 'HP:0034947', 'Altered location of the longitudinal column in the fibrous sheath', 'XPO:0141007', 'abnormally necrotic electrically active cell', 0.40425531914893614, 5.43643956286526, 1.4824674062251753, 'HP:0025461', 'Abnormal cell morphology'),
(290165, 'HP:0034947', 'Altered location of the longitudinal column in the fibrous sheath', 'XPO:0141048', 'abnormally necrotic mitotic cell', 0.40425531914893614, 5.43643956286526, 1.4824674062251753, 'HP:0025461', 'Abnormal cell morphology'),
(290166, 'HP:0034947', 'Altered location of the longitudinal column in the fibrous sheath', 'XPO:0107371', 'abnormal migrating myoblast morphology', 0.4222222222222222, 5.43643956286526, 1.5150530001322648, 'HP:0025461', 'Abnormal cell morphology'),
(290167, 'HP:0034947', 'Altered location of the longitudinal column in the fibrous sheath', 'XPO:0101752', 'abnormal genital system morphology', 0.4782608695652174, 7.005035523447265, 1.8303645486020337, 'UPHENO:0020950', 'abnormal reproductive system morphology'),
(290168, 'HP:0034947', 'Altered location of the longitudinal column in the fibrous sheath', 'XPO:0140068', 'abnormally necrotic myoblast', 0.40425531914893614, 5.43643956286526, 1.4824674062251753, 'HP:0025461', 'Abnormal cell morphology'),
(290169, 'HP:0034947', 'Altered location of the longitudinal column in the fibrous sheath', 'XPO:0102556', 'abnormal spermatozoon morphology', 0.47058823529411764, 6.723205497167461, 1.7787246584088685, 'UPHENO:0087547', 'abnormal reproductive system morphology'),
(290170, 'HP:0034947', 'Altered location of the longitudinal column in the fibrous sheath', 'XPO:0140899', 'abnormally necrotic mucus secreting cell', 0.40425531914893614, 5.43643956286526, 1.4824674062251753, 'HP:0025461', 'Abnormal cell morphology'),
(290171, 'HP:0034947', 'Altered location of the longitudinal column in the fibrous sheath', 'XPO:0103005', 'abnormal oxygen accumulating cell morphology', 0.4418604651162791, 5.43643956286526, 1.5498863551319448, 'HP:0025461', 'Abnormal cell morphology'),
(290172, 'HP:0034947', 'Altered location of the longitudinal column in the fibrous sheath', 'XPO:0141154', 'abnormally necrotic barrier cell', 0.40425531914893614, 5.43643956286526, 1.4824674062251753, 'HP:0025461', 'Abnormal cell morphology'),
(290173, 'HP:0034947', 'Altered location of the longitudinal column in the fibrous sheath', 'XPO:0100765', 'abnormal male genitalia', 0.4782608695652174, 7.005035523447265, 1.8303645486020337, 'HP:0012243', 'Abnormal reproductive system morphology'),
(290174, 'HP:0034947', 'Altered location of the longitudinal column in the fibrous sheath', 'XPO:0102206', 'abnormal gastrula cell morphology', 0.40425531914893614, 5.43643956286526, 1.4824674062251753, 'HP:0025461', 'Abnormal cell morphology'),
(290175, 'HP:0034947', 'Altered location of the longitudinal column in the fibrous sheath', 'XPO:0101658', 'abnormal germ cell morphology', 0.4418604651162791, 5.43643956286526, 1.5498863551319448, 'HP:0025461', 'Abnormal cell morphology'),
(290176, 'HP:0034947', 'Altered location of the longitudinal column in the fibrous sheath', 'XPO:0101636', 'abnormal cell morphology', 0.4634146341463415, 5.43643956286526, 1.587238372483447, 'HP:0025461', 'Abnormal cell morphology'),
(290177, 'HP:0034947', 'Altered location of the longitudinal column in the fibrous sheath', 'XPO:0101740', 'abnormal cell part morphology', 0.40476190476190477, 3.6715585125471644, 1.219059890646631, 'UPHENO:0086172', 'abnormal cell'),
(290178, 'HP:0034947', 'Altered location of the longitudinal column in the fibrous sheath', 'XPO:0103067', 'abnormal paracrine cell morphology', 0.4418604651162791, 5.43643956286526, 1.5498863551319448, 'HP:0025461', 'Abnormal cell morphology'),
(290179, 'HP:0034947', 'Altered location of the longitudinal column in the fibrous sheath', 'XPO:0102965', 'abnormal barrier epithelial cell morphology', 0.4418604651162791, 5.43643956286526, 1.5498863551319448, 'HP:0025461', 'Abnormal cell morphology'),
(290180, 'HP:0034947', 'Altered location of the longitudinal column in the fibrous sheath', 'XPO:0102860', 'abnormal mesenchymal stem cell morphology', 0.4222222222222222, 5.43643956286526, 1.5150530001322648, 'HP:0025461', 'Abnormal cell morphology'),
(290181, 'HP:0034947', 'Altered location of the longitudinal column in the fibrous sheath', 'XPO:0140239', 'abnormally necrotic absorptive cell', 0.40425531914893614, 5.43643956286526, 1.4824674062251753, 'HP:0025461', 'Abnormal cell morphology'),
(290182, 'HP:0034947', 'Altered location of the longitudinal column in the fibrous sheath', 'XPO:0101808', 'abnormal stage VI oocyte morphology', 0.40425531914893614, 5.43643956286526, 1.4824674062251753, 'HP:0025461', 'Abnormal cell morphology'),
(290183, 'HP:0034947', 'Altered location of the longitudinal column in the fibrous sheath', 'XPO:0102869', 'abnormal mucus secreting cell morphology', 0.4418604651162791, 5.43643956286526, 1.5498863551319448, 'HP:0025461', 'Abnormal cell morphology'),
(290184, 'HP:0034947', 'Altered location of the longitudinal column in the fibrous sheath', 'XPO:0102397', 'abnormal male genitalia morphology', 0.4230769230769231, 7.005035523447265, 1.7215309684419309, 'HP:0012243', 'Abnormal reproductive system morphology'),
(290185, 'HP:0034947', 'Altered location of the longitudinal column in the fibrous sheath', 'XPO:0102069', 'abnormal proepicardium morphology', 0.4222222222222222, 5.43643956286526, 1.5150530001322648, 'HP:0025461', 'Abnormal cell morphology'),
(290186, 'HP:0034947', 'Altered location of the longitudinal column in the fibrous sheath', 'XPO:0102531', 'abnormal secondary spermatogonium morphology', 0.4222222222222222, 5.43643956286526, 1.5150530001322648, 'HP:0025461', 'Abnormal cell morphology'),
(290187, 'HP:0034947', 'Altered location of the longitudinal column in the fibrous sheath', 'XPO:0140709', 'abnormally necrotic acid secreting cell', 0.40425531914893614, 5.43643956286526, 1.4824674062251753, 'HP:0025461', 'Abnormal cell morphology'),
(290188, 'HP:0034947', 'Altered location of the longitudinal column in the fibrous sheath', 'XPO:0101232', 'abnormal female genitalia', 0.4782608695652174, 7.005035523447265, 1.8303645486020337, 'UPHENO:0020950', 'abnormal reproductive system morphology'),
(290189, 'HP:0034947', 'Altered location of the longitudinal column in the fibrous sheath', 'XPO:0101940', 'abnormal early embryonic cell morphology', 0.4222222222222222, 5.43643956286526, 1.5150530001322648, 'HP:0025461', 'Abnormal cell morphology'),
(290190, 'HP:0034947', 'Altered location of the longitudinal column in the fibrous sheath', 'XPO:0103112', 'abnormal stage V oocyte morphology', 0.40425531914893614, 5.43643956286526, 1.4824674062251753, 'HP:0025461', 'Abnormal cell morphology'),
(290191, 'HP:0034947', 'Altered location of the longitudinal column in the fibrous sheath', 'XPO:0102872', 'abnormal ciliated non-epidermal cell morphology', 0.4222222222222222, 5.43643956286526, 1.5150530001322648, 'HP:0025461', 'Abnormal cell morphology'),
(290192, 'HP:0034947', 'Altered location of the longitudinal column in the fibrous sheath', 'XPO:0140919', 'abnormally necrotic cementoblast', 0.40425531914893614, 5.43643956286526, 1.4824674062251753, 'HP:0025461', 'Abnormal cell morphology'),
(290193, 'HP:0034947', 'Altered location of the longitudinal column in the fibrous sheath', 'XPO:0101921', 'abnormal chondroblast morphology', 0.4418604651162791, 5.43643956286526, 1.5498863551319448, 'HP:0025461', 'Abnormal cell morphology'),
(290194, 'HP:0034947', 'Altered location of the longitudinal column in the fibrous sheath', 'XPO:0101657', 'abnormal oocyte morphology', 0.4222222222222222, 5.43643956286526, 1.5150530001322648, 'HP:0025461', 'Abnormal cell morphology'),
(290195, 'HP:0034947', 'Altered location of the longitudinal column in the fibrous sheath', 'XPO:0139992', 'abnormally necrotic gamete', 0.4444444444444444, 6.723205497167461, 1.7286096528928754, 'UPHENO:0087547', 'abnormal reproductive system morphology'),
(290196, 'HP:0034947', 'Altered location of the longitudinal column in the fibrous sheath', 'XPO:0102285', 'abnormal myoblast morphology', 0.4418604651162791, 5.43643956286526, 1.5498863551319448, 'HP:0025461', 'Abnormal cell morphology'),
(290197, 'HP:0034947', 'Altered location of the longitudinal column in the fibrous sheath', 'XPO:0102864', 'abnormal female genitalia morphology', 0.4230769230769231, 7.005035523447265, 1.7215309684419309, 'HP:0012243', 'Abnormal reproductive system morphology'),
(290198, 'HP:0034947', 'Altered location of the longitudinal column in the fibrous sheath', 'XPO:0139867', 'abnormally necrotic genital system', 0.43137254901960786, 7.005035523447265, 1.7383267902561792, 'HP:0012243', 'Abnormal reproductive system morphology'),
(290199, 'HP:0034947', 'Altered location of the longitudinal column in the fibrous sheath', 'XPO:0139717', 'abnormally necrotic cell', 0.4318181818181818, 5.43643956286526, 1.532172786470543, 'HP:0025461', 'Abnormal cell morphology'),
(290200, 'HP:0034947', 'Altered location of the longitudinal column in the fibrous sheath', 'XPO:0102165', 'abnormal melanoblast morphology', 0.4418604651162791, 5.43643956286526, 1.5498863551319448, 'HP:0025461', 'Abnormal cell morphology'),
(290201, 'HP:0034947', 'Altered location of the longitudinal column in the fibrous sheath', 'XPO:0140075', 'abnormally necrotic stem cell', 0.40425531914893614, 5.43643956286526, 1.4824674062251753, 'HP:0025461', 'Abnormal cell morphology'),
(290202, 'HP:0034947', 'Altered location of the longitudinal column in the fibrous sheath', 'XPO:0102423', 'abnormal multiciliated cell precursor morphology', 0.4418604651162791, 5.43643956286526, 1.5498863551319448, 'HP:0025461', 'Abnormal cell morphology'),
(290203, 'HP:0034947', 'Altered location of the longitudinal column in the fibrous sheath', 'XPO:0101262', 'abnormal oviduct', 0.44, 7.005035523447265, 1.755624000267938, 'UPHENO:0020950', 'abnormal reproductive system morphology'),
(290204, 'HP:0034947', 'Altered location of the longitudinal column in the fibrous sheath', 'XPO:0101917', 'abnormal progenitor cell morphology', 0.4418604651162791, 5.43643956286526, 1.5498863551319448, 'HP:0025461', 'Abnormal cell morphology'),
(290205, 'HP:0034947', 'Altered location of the longitudinal column in the fibrous sheath', 'XPO:0141065', 'abnormally necrotic paracrine cell', 0.40425531914893614, 5.43643956286526, 1.4824674062251753, 'HP:0025461', 'Abnormal cell morphology'),
(290206, 'HP:0034947', 'Altered location of the longitudinal column in the fibrous sheath', 'XPO:0130929', 'increased size of the polar body', 0.49122807017543857, 10.532569744119352, 2.2746195087073273, 'HP:0012862', 'Abnormal germ cell morphology'),
(290207, 'HP:0034947', 'Altered location of the longitudinal column in the fibrous sheath', 'XPO:0141147', 'abnormally necrotic alkali secreting cell', 0.40425531914893614, 5.43643956286526, 1.4824674062251753, 'HP:0025461', 'Abnormal cell morphology'),
(290208, 'HP:0034947', 'Altered location of the longitudinal column in the fibrous sheath', 'XPO:0101850', 'abnormal epithelial cell morphology', 0.41304347826086957, 5.43643956286526, 1.4984945466703803, 'HP:0025461', 'Abnormal cell morphology'),
(290209, 'HP:0034947', 'Altered location of the longitudinal column in the fibrous sheath', 'XPO:0100666', 'abnormal primary spermatogonium', 0.4067796610169492, 7.005035523447265, 1.6880479778843864, 'HP:0012243', 'Abnormal reproductive system morphology'),
(290210, 'HP:0034947', 'Altered location of the longitudinal column in the fibrous sheath', 'XPO:0101948', 'abnormal gamete morphology', 0.4897959183673469, 6.723205497167461, 1.8146621203016091, 'UPHENO:0087547', 'abnormal reproductive system morphology'),
(290211, 'HP:0034947', 'Altered location of the longitudinal column in the fibrous sheath', 'XPO:0140600', 'abnormally necrotic apoptotic cell', 0.40425531914893614, 5.43643956286526, 1.4824674062251753, 'HP:0025461', 'Abnormal cell morphology'),
(290212, 'HP:0034947', 'Altered location of the longitudinal column in the fibrous sheath', 'XPO:0102323', 'abnormal keratin accumulating cell morphology', 0.4418604651162791, 5.43643956286526, 1.5498863551319448, 'HP:0025461', 'Abnormal cell morphology'),
(290213, 'HP:0034947', 'Altered location of the longitudinal column in the fibrous sheath', 'XPO:0141146', 'abnormally necrotic oxygen accumulating cell', 0.40425531914893614, 5.43643956286526, 1.4824674062251753, 'HP:0025461', 'Abnormal cell morphology'),
(290214, 'HP:0034947', 'Altered location of the longitudinal column in the fibrous sheath', 'XPO:0140381', 'abnormally necrotic ciliated cell', 0.40425531914893614, 5.43643956286526, 1.4824674062251753, 'HP:0025461', 'Abnormal cell morphology'),
(290215, 'HP:0034947', 'Altered location of the longitudinal column in the fibrous sheath', 'XPO:0103167', 'abnormal absorptive cell morphology', 0.4418604651162791, 5.43643956286526, 1.5498863551319448, 'HP:0025461', 'Abnormal cell morphology'),
(290216, 'HP:0034947', 'Altered location of the longitudinal column in the fibrous sheath', 'XPO:0101939', 'abnormal blastomere morphology', 0.40425531914893614, 5.43643956286526, 1.4824674062251753, 'HP:0025461', 'Abnormal cell morphology'),
(290217, 'HP:0034947', 'Altered location of the longitudinal column in the fibrous sheath', 'XPO:0102764', 'abnormal apoptotic cell morphology', 0.4418604651162791, 5.43643956286526, 1.5498863551319448, 'HP:0025461', 'Abnormal cell morphology'),
(290218, 'HP:0034947', 'Altered location of the longitudinal column in the fibrous sheath', 'XPO:0139929', 'abnormally necrotic barrier epithelial cell', 0.40425531914893614, 5.43643956286526, 1.4824674062251753, 'HP:0025461', 'Abnormal cell morphology'),
(290219, 'HP:0034947', 'Altered location of the longitudinal column in the fibrous sheath', 'XPO:0102873', 'abnormal nucleate erythrocyte morphology', 0.4418604651162791, 5.43643956286526, 1.5498863551319448, 'HP:0025461', 'Abnormal cell morphology'),
(290220, 'HP:0034947', 'Altered location of the longitudinal column in the fibrous sheath', 'XPO:0102929', 'abnormal barrier cell morphology', 0.4418604651162791, 5.43643956286526, 1.5498863551319448, 'HP:0025461', 'Abnormal cell morphology'),
(290221, 'HP:0034947', 'Altered location of the longitudinal column in the fibrous sheath', 'XPO:0102998', 'abnormal morula cell morphology', 0.40425531914893614, 5.43643956286526, 1.4824674062251753, 'HP:0025461', 'Abnormal cell morphology'),
(290222, 'HP:0034947', 'Altered location of the longitudinal column in the fibrous sheath', 'XPO:0140533', 'abnormally necrotic myelin accumulating cell', 0.40425531914893614, 5.43643956286526, 1.4824674062251753, 'HP:0025461', 'Abnormal cell morphology'),
(290223, 'HP:0034947', 'Altered location of the longitudinal column in the fibrous sheath', 'XPO:0129455', 'decreased size of the polar body', 0.49122807017543857, 10.532569744119352, 2.2746195087073273, 'HP:0012862', 'Abnormal germ cell morphology'),
(290224, 'HP:0034947', 'Altered location of the longitudinal column in the fibrous sheath', 'XPO:0102648', 'abnormal egg morphology', 0.47058823529411764, 6.723205497167461, 1.7787246584088685, 'UPHENO:0087547', 'abnormal reproductive system morphology'),
(290225, 'HP:0034947', 'Altered location of the longitudinal column in the fibrous sheath', 'XPO:0140723', 'abnormally necrotic polar body', 0.5714285714285714, 10.532569744119352, 2.453285813425316, 'HP:0012862', 'Abnormal germ cell morphology'),
(290226, 'HP:0034947', 'Altered location of the longitudinal column in the fibrous sheath', 'XPO:0103100', 'abnormal stage I oocyte morphology', 0.40425531914893614, 5.43643956286526, 1.4824674062251753, 'HP:0025461', 'Abnormal cell morphology'),
(290227, 'HP:0034947', 'Altered location of the longitudinal column in the fibrous sheath', 'XPO:0102534', 'abnormal spermatocyte morphology', 0.4222222222222222, 5.43643956286526, 1.5150530001322648, 'HP:0025461', 'Abnormal cell morphology'),
(290228, 'HP:0034947', 'Altered location of the longitudinal column in the fibrous sheath', 'XPO:0140010', 'abnormally necrotic zygote', 0.40425531914893614, 5.43643956286526, 1.4824674062251753, 'HP:0025461', 'Abnormal cell morphology'),
(290229, 'HP:0034947', 'Altered location of the longitudinal column in the fibrous sheath', 'XPO:0102636', 'abnormal acid secreting cell morphology', 0.4418604651162791, 5.43643956286526, 1.5498863551319448, 'HP:0025461', 'Abnormal cell morphology'),
(290230, 'HP:0034947', 'Altered location of the longitudinal column in the fibrous sheath', 'XPO:0140760', 'abnormally necrotic spermatozoon', 0.42105263157894735, 6.723205497167461, 1.6825050868358185, 'UPHENO:0087547', 'abnormal reproductive system morphology'),
(290231, 'HP:0034947', 'Altered location of the longitudinal column in the fibrous sheath', 'XPO:0102306', 'abnormal secondary oogonium morphology', 0.4222222222222222, 5.43643956286526, 1.5150530001322648, 'HP:0025461', 'Abnormal cell morphology'),
(290232, 'HP:0034947', 'Altered location of the longitudinal column in the fibrous sheath', 'XPO:0103080', 'abnormal myelin accumulating cell morphology', 0.4418604651162791, 5.43643956286526, 1.5498863551319448, 'HP:0025461', 'Abnormal cell morphology'),
(290233, 'HP:0034947', 'Altered location of the longitudinal column in the fibrous sheath', 'XPO:0102608', 'abnormal multiciliated cell morphology', 0.4222222222222222, 5.43643956286526, 1.5150530001322648, 'HP:0025461', 'Abnormal cell morphology'),
(290234, 'HP:0034947', 'Altered location of the longitudinal column in the fibrous sheath', 'XPO:0140803', 'abnormally necrotic pericyte', 0.40425531914893614, 5.43643956286526, 1.4824674062251753, 'HP:0025461', 'Abnormal cell morphology'),
(290235, 'HP:0034947', 'Altered location of the longitudinal column in the fibrous sheath', 'XPO:0102270', 'abnormal polar body morphology', 0.6222222222222222, 10.532569744119352, 2.559999795292274, 'HP:0012862', 'Abnormal germ cell morphology'),
(290236, 'HP:0034947', 'Altered location of the longitudinal column in the fibrous sheath', 'XPO:0141203', 'abnormally necrotic exocrine cell', 0.40425531914893614, 5.43643956286526, 1.4824674062251753, 'HP:0025461', 'Abnormal cell morphology'),
(290237, 'HP:0034947', 'Altered location of the longitudinal column in the fibrous sheath', 'XPO:0128384', 'decreased size of the genital system', 0.41509433962264153, 7.005035523447265, 1.705212771075354, 'HP:0012243', 'Abnormal reproductive system morphology'),
(290238, 'HP:0034947', 'Altered location of the longitudinal column in the fibrous sheath', 'XPO:0139839', 'abnormally necrotic progenitor cell', 0.40425531914893614, 5.43643956286526, 1.4824674062251753, 'HP:0025461', 'Abnormal cell morphology'),
(290239, 'HP:0034947', 'Altered location of the longitudinal column in the fibrous sheath', 'XPO:0101804', 'abnormal stem cell morphology', 0.4418604651162791, 5.43643956286526, 1.5498863551319448, 'HP:0025461', 'Abnormal cell morphology'),
(290240, 'HP:0034947', 'Altered location of the longitudinal column in the fibrous sheath', 'XPO:0101969', 'abnormal zygote morphology', 0.4418604651162791, 5.43643956286526, 1.5498863551319448, 'HP:0025461', 'Abnormal cell morphology'),
(290241, 'HP:0034947', 'Altered location of the longitudinal column in the fibrous sheath', 'XPO:0140752', 'abnormally necrotic melanoblast', 0.40425531914893614, 5.43643956286526, 1.4824674062251753, 'HP:0025461', 'Abnormal cell morphology'),
(290242, 'HP:0034947', 'Altered location of the longitudinal column in the fibrous sheath', 'XPO:0103130', 'abnormal stage II oocyte morphology', 0.40425531914893614, 5.43643956286526, 1.4824674062251753, 'HP:0025461', 'Abnormal cell morphology'),
(290243, 'HP:0034947', 'Altered location of the longitudinal column in the fibrous sheath', 'XPO:0140647', 'abnormally necrotic nucleate erythrocyte', 0.40425531914893614, 5.43643956286526, 1.4824674062251753, 'HP:0025461', 'Abnormal cell morphology'),
(290244, 'HP:0034947', 'Altered location of the longitudinal column in the fibrous sheath', 'XPO:0102549', 'abnormal stage III oocyte morphology', 0.40425531914893614, 5.43643956286526, 1.4824674062251753, 'HP:0025461', 'Abnormal cell morphology'),
(290245, 'HP:0034947', 'Altered location of the longitudinal column in the fibrous sheath', 'XPO:0103099', 'abnormal alkali secreting cell morphology', 0.4418604651162791, 5.43643956286526, 1.5498863551319448, 'HP:0025461', 'Abnormal cell morphology'),
(290246, 'HP:0034947', 'Altered location of the longitudinal column in the fibrous sheath', 'XPO:0140471', 'abnormally necrotic multiciliated cell precursor', 0.40425531914893614, 5.43643956286526, 1.4824674062251753, 'HP:0025461', 'Abnormal cell morphology'),
(290247, 'HP:0034947', 'Altered location of the longitudinal column in the fibrous sheath', 'XPO:0102147', 'abnormal somatic stem cell morphology', 0.4222222222222222, 5.43643956286526, 1.5150530001322648, 'HP:0025461', 'Abnormal cell morphology'),
(290248, 'HP:0034947', 'Altered location of the longitudinal column in the fibrous sheath', 'XPO:0102958', 'abnormal cementoblast morphology', 0.4418604651162791, 5.43643956286526, 1.5498863551319448, 'HP:0025461', 'Abnormal cell morphology'),
(290249, 'HP:0034947', 'Altered location of the longitudinal column in the fibrous sheath', 'XPO:0102109', 'abnormal pericyte morphology', 0.4418604651162791, 5.43643956286526, 1.5498863551319448, 'HP:0025461', 'Abnormal cell morphology'),
(290250, 'HP:0034947', 'Altered location of the longitudinal column in the fibrous sheath', 'XPO:0140868', 'abnormally necrotic chondroblast', 0.40425531914893614, 5.43643956286526, 1.4824674062251753, 'HP:0025461', 'Abnormal cell morphology'),
(290251, 'HP:0034947', 'Altered location of the longitudinal column in the fibrous sheath', 'XPO:0139759', 'abnormally necrotic germ cell', 0.40425531914893614, 5.43643956286526, 1.4824674062251753, 'HP:0025461', 'Abnormal cell morphology'),
(290252, 'HP:0034947', 'Altered location of the longitudinal column in the fibrous sheath', 'XPO:0140496', 'abnormally necrotic egg', 0.42105263157894735, 6.723205497167461, 1.6825050868358185, 'UPHENO:0087547', 'abnormal reproductive system morphology'),
(290253, 'HP:0034947', 'Altered location of the longitudinal column in the fibrous sheath', 'XPO:0102258', 'abnormal primordial germ cell morphology', 0.4222222222222222, 5.43643956286526, 1.5150530001322648, 'HP:0025461', 'Abnormal cell morphology'),
(290254, 'HP:0034947', 'Altered location of the longitudinal column in the fibrous sheath', 'XPO:0102386', 'abnormal electrically active cell morphology', 0.4418604651162791, 5.43643956286526, 1.5498863551319448, 'HP:0025461', 'Abnormal cell morphology'),
(290255, 'HP:0034947', 'Altered location of the longitudinal column in the fibrous sheath', 'XPO:0102745', 'abnormal stage IV oocyte morphology', 0.40425531914893614, 5.43643956286526, 1.4824674062251753, 'HP:0025461', 'Abnormal cell morphology'),
(290256, 'HP:0034947', 'Altered location of the longitudinal column in the fibrous sheath', 'XPO:0102434', 'abnormal exocrine cell morphology', 0.4418604651162791, 5.43643956286526, 1.5498863551319448, 'HP:0025461', 'Abnormal cell morphology'),
(290257, 'HP:0034947', 'Altered location of the longitudinal column in the fibrous sheath', 'XPO:0102181', 'abnormal mitotic cell morphology', 0.4418604651162791, 5.43643956286526, 1.5498863551319448, 'HP:0025461', 'Abnormal cell morphology'),
(290258, 'HP:0034947', 'Altered location of the longitudinal column in the fibrous sheath', 'XPO:0102336', 'abnormal Merkel cell morphology', 0.4418604651162791, 5.43643956286526, 1.5498863551319448, 'HP:0025461', 'Abnormal cell morphology'),
(290259, 'HP:0010620', 'Malar prominence', 'XPO:0140644', 'abnormally necrotic otic region', 0.40789473684210525, 7.024697770424301, 1.6927307076031153, 'HP:0000929', 'Abnormal skull morphology'),
(290260, 'HP:0010620', 'Malar prominence', 'XPO:0140560', 'abnormally necrotic orbital region', 0.5405405405405406, 11.582693223545188, 2.5021820988829675, 'HP:3000030', 'Abnormal morphology of bony orbit of skull'),
(290261, 'HP:0010620', 'Malar prominence', 'XPO:0140672', 'abnormally necrotic olfactory region', 0.40789473684210525, 7.024697770424301, 1.6927307076031153, 'HP:0000929', 'Abnormal skull morphology'),
(290262, 'HP:0010620', 'Malar prominence', 'XPO:0130701', 'increased size of the upper jaw', 0.4367816091954023, 8.81758714901448, 1.9624881921089983, 'UPHENO:0087585', 'abnormal midface morphology'),
(290263, 'HP:0010620', 'Malar prominence', 'XPO:0102921', 'abnormal orbital region morphology', 0.5797101449275363, 11.582693223545188, 2.5912554423044774, 'HP:3000030', 'Abnormal morphology of bony orbit of skull'),
(290264, 'HP:0010620', 'Malar prominence', 'XPO:0141201', 'abnormally necrotic sphenoid region', 0.40789473684210525, 7.024697770424301, 1.6927307076031153, 'HP:0000929', 'Abnormal skull morphology'),
(290265, 'HP:0010620', 'Malar prominence', 'XPO:0129225', 'decreased size of the upper jaw', 0.4367816091954023, 8.81758714901448, 1.9624881921089983, 'UPHENO:0087585', 'abnormal midface morphology'),
(290266, 'HP:0010620', 'Malar prominence', 'XPO:0140639', 'abnormally necrotic upper jaw', 0.4470588235294118, 8.81758714901448, 1.9854420508306139, 'UPHENO:0087585', 'abnormal midface morphology'),
(290267, 'HP:0010620', 'Malar prominence', 'XPO:0128905', 'decreased size of the occipital region', 0.4025974025974026, 7.024697770424301, 1.6817030286006471, 'HP:0000929', 'Abnormal skull morphology'),
(290268, 'HP:0010620', 'Malar prominence', 'XPO:0128846', 'decreased size of the choana', 0.43037974683544306, 7.024697770424301, 1.7387603768290534, 'HP:0000929', 'Abnormal skull morphology'),
(290269, 'HP:0010620', 'Malar prominence', 'XPO:0103138', 'abnormal upper jaw morphology', 0.475, 8.81758714901448, 2.0465468222793923, 'UPHENO:0087585', 'abnormal midface morphology'),
(290270, 'HP:0010620', 'Malar prominence', 'XPO:0101659', 'abnormal lower jaw morphology', 0.45, 8.057231734572694, 1.904141349941677, 'UPHENO:0084457', 'abnormal facial skeleton morphology'),
(290271, 'HP:0010620', 'Malar prominence', 'XPO:0128880', 'decreased size of the lower jaw', 0.41379310344827586, 8.057231734572694, 1.8259317962757453, 'UPHENO:0084457', 'abnormal facial skeleton morphology'),
(290272, 'HP:0010620', 'Malar prominence', 'XPO:0102828', 'abnormal occipital region morphology', 0.44285714285714284, 7.024697770424301, 1.7637850163909, 'HP:0000929', 'Abnormal skull morphology'),
(290273, 'HP:0010620', 'Malar prominence', 'XPO:0102401', 'abnormal neurocranium morphology', 0.43661971830985913, 7.024697770424301, 1.7513199484202062, 'HP:0000929', 'Abnormal skull morphology'),
(290274, 'HP:0010620', 'Malar prominence', 'XPO:0130324', 'increased size of the choana', 0.43037974683544306, 7.024697770424301, 1.7387603768290534, 'HP:0000929', 'Abnormal skull morphology'),
(290275, 'HP:0010620', 'Malar prominence', 'XPO:0102351', 'abnormal sphenoid region morphology', 0.43661971830985913, 7.024697770424301, 1.7513199484202062, 'HP:0000929', 'Abnormal skull morphology'),
(290276, 'HP:0010620', 'Malar prominence', 'XPO:0130767', 'increased size of the orbital region', 0.5128205128205128, 11.582693223545188, 2.437179246329888, 'HP:3000030', 'Abnormal morphology of bony orbit of skull'),
(290277, 'HP:0010620', 'Malar prominence', 'XPO:0130358', 'increased size of the lower jaw', 0.41379310344827586, 8.057231734572694, 1.8259317962757453, 'UPHENO:0084457', 'abnormal facial skeleton morphology'),
(290278, 'HP:0010620', 'Malar prominence', 'XPO:0103152', 'abnormal otic region morphology', 0.43661971830985913, 7.024697770424301, 1.7513199484202062, 'HP:0000929', 'Abnormal skull morphology'),
(290279, 'HP:0010620', 'Malar prominence', 'XPO:0102564', 'abnormal olfactory region morphology', 0.43661971830985913, 7.024697770424301, 1.7513199484202062, 'HP:0000929', 'Abnormal skull morphology'),
(290280, 'HP:0010620', 'Malar prominence', 'XPO:0141185', 'abnormally necrotic occipital region', 0.41333333333333333, 7.024697770424301, 1.7039782114536297, 'HP:0000929', 'Abnormal skull morphology'),
(290281, 'HP:0010620', 'Malar prominence', 'XPO:0103381', 'increased size of the head', 0.4189189189189189, 7.024697770424301, 1.7154529418548001, 'HP:0000929', 'Abnormal skull morphology'),
(290282, 'HP:0010620', 'Malar prominence', 'XPO:0130383', 'increased size of the occipital region', 0.4025974025974026, 7.024697770424301, 1.6817030286006471, 'HP:0000929', 'Abnormal skull morphology'),
(290283, 'HP:0010620', 'Malar prominence', 'XPO:0129291', 'decreased size of the orbital region', 0.5128205128205128, 11.582693223545188, 2.437179246329888, 'HP:3000030', 'Abnormal morphology of bony orbit of skull'),
(290284, 'HP:0010620', 'Malar prominence', 'XPO:0100420', 'abnormal choana', 0.40298507462686567, 5.788671267106304, 1.5273336644509696, 'UPHENO:0087472', 'abnormal face morphology'),
(290285, 'HP:0010620', 'Malar prominence', 'XPO:0140926', 'abnormally necrotic neurocranium', 0.40789473684210525, 7.024697770424301, 1.6927307076031153, 'HP:0000929', 'Abnormal skull morphology'),
(290286, 'HP:0010620', 'Malar prominence', 'XPO:0102052', 'abnormal choana morphology', 0.4657534246575342, 7.024697770424301, 1.8088054189876985, 'HP:0000929', 'Abnormal skull morphology'),
(290287, 'HP:0010620', 'Malar prominence', 'XPO:0140897', 'abnormally necrotic lower jaw', 0.4235294117647059, 8.057231734572694, 1.847288449862526, 'UPHENO:0084457', 'abnormal facial skeleton morphology'),
(290288, 'HP:0031014', 'Arteria lusoria', 'XPO:0129954', 'increased size of the ischiadic vein', 0.4067796610169492, 7.803720102857406, 1.7816830857679173, 'HP:0033353', 'Abnormal blood vessel morphology'),
(290289, 'HP:0031014', 'Arteria lusoria', 'XPO:0128662', 'decreased size of the Jacobsons vein', 0.4067796610169492, 7.803720102857406, 1.7816830857679173, 'HP:0033353', 'Abnormal blood vessel morphology'),
(290290, 'HP:0031014', 'Arteria lusoria', 'XPO:0102645', 'abnormal ventral caudal lymphatic vessel morphology', 0.4339622641509434, 6.65602285090012, 1.6995478065112006, 'HP:0025015', 'Abnormal vascular morphology'),
(290291, 'HP:0031014', 'Arteria lusoria', 'XPO:0102154', 'abnormal subinterstitial vein morphology', 0.48, 7.803720102857406, 1.9354032265581131, 'HP:0033353', 'Abnormal blood vessel morphology'),
(290292, 'HP:0031014', 'Arteria lusoria', 'XPO:0128028', 'decreased size of the vein', 0.42857142857142855, 7.803720102857406, 1.828784151465988, 'HP:0033353', 'Abnormal blood vessel morphology'),
(290293, 'HP:0031014', 'Arteria lusoria', 'XPO:0101995', 'abnormal cardiovascular system morphology', 0.48717948717948717, 5.9590888072311134, 1.7038620334885908, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(290294, 'HP:0031014', 'Arteria lusoria', 'XPO:0102424', 'abnormal capillary morphology', 0.5, 7.803720102857406, 1.9753126465014856, 'HP:0033353', 'Abnormal blood vessel morphology'),
(290295, 'HP:0031014', 'Arteria lusoria', 'XPO:0140735', 'abnormally necrotic lymph vessel', 0.4107142857142857, 6.65602285090012, 1.6533976142795799, 'HP:0025015', 'Abnormal vascular morphology'),
(290296, 'HP:0031014', 'Arteria lusoria', 'XPO:0102613', 'abnormal dorsal longitudinal anastomosing vessel morphology', 0.5111111111111111, 6.65602285090012, 1.844442255779374, 'HP:0025015', 'Abnormal vascular morphology'),
(290297, 'HP:0031014', 'Arteria lusoria', 'XPO:0129470', 'decreased size of the subinterstitial vein', 0.4067796610169492, 7.803720102857406, 1.7816830857679173, 'HP:0033353', 'Abnormal blood vessel morphology'),
(290298, 'HP:0031014', 'Arteria lusoria', 'XPO:0102748', 'abnormal lateral vein morphology', 0.43636363636363634, 7.803720102857406, 1.8453345716283722, 'HP:0033353', 'Abnormal blood vessel morphology'),
(290299, 'HP:0031014', 'Arteria lusoria', 'XPO:0102553', 'abnormal dorsal caudal lymphatic vessel morphology', 0.4339622641509434, 6.65602285090012, 1.6995478065112006, 'HP:0025015', 'Abnormal vascular morphology'),
(290300, 'HP:0031014', 'Arteria lusoria', 'XPO:0100780', 'abnormal vascular plexus', 0.41025641025641024, 5.809304221129108, 1.5437954190396599, 'UPHENO:0002678', 'abnormal vasculature'),
(290301, 'HP:0031014', 'Arteria lusoria', 'XPO:0101711', 'abnormal dorsal aorta morphology', 0.4262295081967213, 8.750570396338642, 1.93125640878476, 'HP:0011004', 'Abnormal systemic arterial morphology'),
(290302, 'HP:0031014', 'Arteria lusoria', 'XPO:0129579', 'increased size of the artery', 0.41818181818181815, 6.65602285090012, 1.6683607936082474, 'HP:0025015', 'Abnormal vascular morphology'),
(290303, 'HP:0031014', 'Arteria lusoria', 'XPO:0139730', 'abnormally necrotic vein', 0.4444444444444444, 7.803720102857406, 1.8623426230729947, 'HP:0033353', 'Abnormal blood vessel morphology'),
(290304, 'HP:0031014', 'Arteria lusoria', 'XPO:0103119', 'abnormal epigastric artery morphology', 0.42592592592592593, 6.65602285090012, 1.683737715843461, 'HP:0025015', 'Abnormal vascular morphology'),
(290305, 'HP:0031014', 'Arteria lusoria', 'XPO:0128922', 'decreased size of the dorsal longitudinal anastomosing vessel', 0.4339622641509434, 6.65602285090012, 1.6995478065112006, 'HP:0025015', 'Abnormal vascular morphology'),
(290306, 'HP:0031014', 'Arteria lusoria', 'XPO:0101770', 'abnormal trunk vasculature morphology', 0.41304347826086957, 5.9590888072311134, 1.5688730886225806, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(290307, 'HP:0031014', 'Arteria lusoria', 'XPO:0101976', 'abnormal portion of organism substance morphology', 0.41935483870967744, 2.786899518863159, 1.0810641970914296, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(290308, 'HP:0031014', 'Arteria lusoria', 'XPO:0130851', 'increased size of the dorsal longitudinal anastomosing vessel - right branch', 0.4107142857142857, 6.65602285090012, 1.6533976142795799, 'HP:0025015', 'Abnormal vascular morphology'),
(290309, 'HP:0031014', 'Arteria lusoria', 'XPO:0103063', 'abnormal ischiadic artery morphology', 0.46938775510204084, 6.65602285090012, 1.7675563990696006, 'HP:0025015', 'Abnormal vascular morphology'),
(290310, 'HP:0031014', 'Arteria lusoria', 'XPO:0102284', 'abnormal medial cardinal vein morphology', 0.43636363636363634, 7.803720102857406, 1.8453345716283722, 'HP:0033353', 'Abnormal blood vessel morphology'),
(290311, 'HP:0031014', 'Arteria lusoria', 'XPO:0130014', 'increased size of the vascular plexus', 0.42592592592592593, 6.65602285090012, 1.683737715843461, 'HP:0025015', 'Abnormal vascular morphology'),
(290312, 'HP:0031014', 'Arteria lusoria', 'XPO:0129961', 'increased size of the circulatory system', 0.40425531914893614, 5.9590888072311134, 1.552093214856655, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(290313, 'HP:0031014', 'Arteria lusoria', 'XPO:0141046', 'abnormally necrotic vertebral artery', 0.4107142857142857, 6.65602285090012, 1.6533976142795799, 'HP:0025015', 'Abnormal vascular morphology'),
(290314, 'HP:0031014', 'Arteria lusoria', 'XPO:0102993', 'abnormal musculoabdominal vein morphology', 0.43636363636363634, 7.803720102857406, 1.8453345716283722, 'HP:0033353', 'Abnormal blood vessel morphology'),
(290315, 'HP:0031014', 'Arteria lusoria', 'XPO:0102425', 'abnormal omphalomesenteric vein morphology', 0.41379310344827586, 7.803720102857406, 1.7969767833233308, 'HP:0033353', 'Abnormal blood vessel morphology'),
(290316, 'HP:0031014', 'Arteria lusoria', 'XPO:0102889', 'abnormal coeliaco-mesenteric artery morphology', 0.42592592592592593, 6.65602285090012, 1.683737715843461, 'HP:0025015', 'Abnormal vascular morphology'),
(290317, 'HP:0031014', 'Arteria lusoria', 'XPO:0103215', 'abnormal truncus arteriosus morphology', 0.5111111111111111, 6.65602285090012, 1.844442255779374, 'HP:0025015', 'Abnormal vascular morphology'),
(290318, 'HP:0031014', 'Arteria lusoria', 'XPO:0128030', 'decreased size of the blood vessel', 0.46, 6.65602285090012, 1.7497915622765061, 'HP:0025015', 'Abnormal vascular morphology'),
(290319, 'HP:0031014', 'Arteria lusoria', 'XPO:0101724', 'abnormal venous endothelium morphology', 0.4107142857142857, 6.65602285090012, 1.6533976142795799, 'HP:0025015', 'Abnormal vascular morphology'),
(290320, 'HP:0031014', 'Arteria lusoria', 'XPO:0128993', 'decreased size of the intersomitic vessel', 0.40350877192982454, 6.65602285090012, 1.6388299504535415, 'HP:0025015', 'Abnormal vascular morphology'),
(290321, 'HP:0031014', 'Arteria lusoria', 'XPO:0101956', 'abnormal intersomitic vessel morphology', 0.46938775510204084, 6.65602285090012, 1.7675563990696006, 'HP:0025015', 'Abnormal vascular morphology'),
(290322, 'HP:0031014', 'Arteria lusoria', 'XPO:0130943', 'increased size of the subinterstitial vein', 0.4067796610169492, 7.803720102857406, 1.7816830857679173, 'HP:0033353', 'Abnormal blood vessel morphology'),
(290323, 'HP:0031014', 'Arteria lusoria', 'XPO:0139803', 'abnormally necrotic aorta', 0.4262295081967213, 8.750570396338642, 1.93125640878476, 'HP:0011004', 'Abnormal systemic arterial morphology'),
(290324, 'HP:0031014', 'Arteria lusoria', 'XPO:0130150', 'increased size of the capillary', 0.42857142857142855, 7.803720102857406, 1.828784151465988, 'HP:0033353', 'Abnormal blood vessel morphology'),
(290325, 'HP:0031014', 'Arteria lusoria', 'XPO:0101675', 'abnormal vein morphology', 0.5, 7.803720102857406, 1.9753126465014856, 'HP:0033353', 'Abnormal blood vessel morphology'),
(290326, 'HP:0031014', 'Arteria lusoria', 'XPO:0128093', 'decreased size of the aorta', 0.4126984126984127, 8.750570396338642, 1.900354312430889, 'HP:0011004', 'Abnormal systemic arterial morphology'),
(290327, 'HP:0031014', 'Arteria lusoria', 'XPO:0130772', 'increased size of the truncus arteriosus', 0.4339622641509434, 6.65602285090012, 1.6995478065112006, 'HP:0025015', 'Abnormal vascular morphology'),
(290328, 'HP:0031014', 'Arteria lusoria', 'XPO:0141554', 'abnormal blood vessel morphology in the regenerating hindlimb', 0.46938775510204084, 6.65602285090012, 1.7675563990696006, 'HP:0025015', 'Abnormal vascular morphology'),
(290329, 'HP:0031014', 'Arteria lusoria', 'XPO:0129008', 'decreased size of the branchial vein', 0.4067796610169492, 7.803720102857406, 1.7816830857679173, 'HP:0033353', 'Abnormal blood vessel morphology'),
(290330, 'HP:0031014', 'Arteria lusoria', 'XPO:0140220', 'abnormally necrotic tail vasculature', 0.40350877192982454, 6.65602285090012, 1.6388299504535415, 'HP:0025015', 'Abnormal vascular morphology'),
(290331, 'HP:0031014', 'Arteria lusoria', 'XPO:0141029', 'abnormally necrotic subinterstitial vein', 0.42105263157894735, 7.803720102857406, 1.8126712016837594, 'HP:0033353', 'Abnormal blood vessel morphology'),
(290332, 'HP:0031014', 'Arteria lusoria', 'XPO:0100981', 'abnormal dorsal longitudinal anastomosing vessel', 0.41025641025641024, 5.809304221129108, 1.5437954190396599, 'UPHENO:0002678', 'abnormal vasculature'),
(290333, 'HP:0031014', 'Arteria lusoria', 'XPO:0101740', 'abnormal cell part morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(290334, 'HP:0031014', 'Arteria lusoria', 'XPO:0140809', 'abnormally necrotic truncus arteriosus', 0.45098039215686275, 6.65602285090012, 1.732551816109399, 'HP:0025015', 'Abnormal vascular morphology'),
(290335, 'HP:0031014', 'Arteria lusoria', 'XPO:0102329', 'abnormal caudal artery morphology', 0.43333333333333335, 8.750570396338642, 1.9472837077358327, 'HP:0011004', 'Abnormal systemic arterial morphology'),
(290336, 'HP:0031014', 'Arteria lusoria', 'XPO:0102363', 'abnormal arterial endothelium morphology', 0.4107142857142857, 6.65602285090012, 1.6533976142795799, 'HP:0025015', 'Abnormal vascular morphology'),
(290337, 'HP:0031014', 'Arteria lusoria', 'XPO:0128671', 'decreased size of the capillary', 0.42857142857142855, 7.803720102857406, 1.828784151465988, 'HP:0033353', 'Abnormal blood vessel morphology'),
(290338, 'HP:0031014', 'Arteria lusoria', 'XPO:0128032', 'decreased size of the cardiovascular system', 0.40425531914893614, 5.9590888072311134, 1.552093214856655, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(290339, 'HP:0031014', 'Arteria lusoria', 'XPO:0101708', 'abnormal artery morphology', 0.48936170212765956, 6.65602285090012, 1.8047721938563548, 'HP:0025015', 'Abnormal vascular morphology'),
(290340, 'HP:0031014', 'Arteria lusoria', 'XPO:0141223', 'abnormally necrotic Jacobsons vein', 0.42105263157894735, 7.803720102857406, 1.8126712016837594, 'HP:0033353', 'Abnormal blood vessel morphology'),
(290341, 'HP:0031014', 'Arteria lusoria', 'XPO:0101769', 'abnormal cardinal vein morphology', 0.46153846153846156, 7.803720102857406, 1.8978190036327416, 'HP:0033353', 'Abnormal blood vessel morphology'),
(290342, 'HP:0031014', 'Arteria lusoria', 'XPO:0103156', 'abnormal ventral blood island border morphology', 0.41818181818181815, 6.65602285090012, 1.6683607936082474, 'HP:0025015', 'Abnormal vascular morphology'),
(290343, 'HP:0031014', 'Arteria lusoria', 'XPO:0102121', 'abnormal vitelline vein morphology', 0.41379310344827586, 7.803720102857406, 1.7969767833233308, 'HP:0033353', 'Abnormal blood vessel morphology'),
(290344, 'HP:0031014', 'Arteria lusoria', 'XPO:0140187', 'abnormally necrotic intersomitic vessel', 0.41818181818181815, 6.65602285090012, 1.6683607936082474, 'HP:0025015', 'Abnormal vascular morphology'),
(290345, 'HP:0031014', 'Arteria lusoria', 'XPO:0140755', 'abnormally necrotic vascular plexus', 0.4423076923076923, 6.65602285090012, 1.7158117924553669, 'HP:0025015', 'Abnormal vascular morphology'),
(290346, 'HP:0031014', 'Arteria lusoria', 'XPO:0139829', 'abnormally necrotic artery', 0.4339622641509434, 6.65602285090012, 1.6995478065112006, 'HP:0025015', 'Abnormal vascular morphology'),
(290347, 'HP:0031014', 'Arteria lusoria', 'XPO:0140595', 'abnormally necrotic dorsal longitudinal anastomosing vessel', 0.45098039215686275, 6.65602285090012, 1.732551816109399, 'HP:0025015', 'Abnormal vascular morphology'),
(290348, 'HP:0031014', 'Arteria lusoria', 'XPO:0100054', 'abnormal blood vessel', 0.42105263157894735, 5.809304221129108, 1.5639766078650594, 'UPHENO:0002678', 'abnormal vasculature'),
(290349, 'HP:0031014', 'Arteria lusoria', 'XPO:0139747', 'abnormally necrotic head vasculature', 0.40350877192982454, 6.65602285090012, 1.6388299504535415, 'HP:0025015', 'Abnormal vascular morphology'),
(290350, 'HP:0031014', 'Arteria lusoria', 'XPO:0139811', 'abnormally necrotic circulatory system', 0.4222222222222222, 5.9590888072311134, 1.5862092291399303, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(290351, 'HP:0031014', 'Arteria lusoria', 'XPO:0101829', 'abnormal subclavian vein morphology', 0.43636363636363634, 7.803720102857406, 1.8453345716283722, 'HP:0033353', 'Abnormal blood vessel morphology'),
(290352, 'HP:0031014', 'Arteria lusoria', 'XPO:0101712', 'abnormal aorta morphology', 0.48148148148148145, 8.750570396338642, 2.0526172556609583, 'HP:0011004', 'Abnormal systemic arterial morphology'),
(290353, 'HP:0031014', 'Arteria lusoria', 'XPO:0140530', 'abnormally necrotic ischiadic artery', 0.4107142857142857, 6.65602285090012, 1.6533976142795799, 'HP:0025015', 'Abnormal vascular morphology'),
(290354, 'HP:0031014', 'Arteria lusoria', 'XPO:0103189', 'abnormal Jacobsons vein morphology', 0.48, 7.803720102857406, 1.9354032265581131, 'HP:0033353', 'Abnormal blood vessel morphology'),
(290355, 'HP:0031014', 'Arteria lusoria', 'XPO:0129508', 'increased size of the vein', 0.42857142857142855, 7.803720102857406, 1.828784151465988, 'HP:0033353', 'Abnormal blood vessel morphology'),
(290356, 'HP:0031014', 'Arteria lusoria', 'XPO:0130470', 'increased size of the intersomitic vessel', 0.40350877192982454, 6.65602285090012, 1.6388299504535415, 'HP:0025015', 'Abnormal vascular morphology'),
(290357, 'HP:0031014', 'Arteria lusoria', 'XPO:0100043', 'abnormal vein', 0.41025641025641024, 5.809304221129108, 1.5437954190396599, 'UPHENO:0002678', 'abnormal vasculature'),
(290358, 'HP:0031014', 'Arteria lusoria', 'XPO:0102421', 'abnormal occipitovertebral artery morphology', 0.46938775510204084, 6.65602285090012, 1.7675563990696006, 'HP:0025015', 'Abnormal vascular morphology'),
(290359, 'HP:0031014', 'Arteria lusoria', 'XPO:0103212', 'abnormal cutaneous magnus morphology', 0.43636363636363634, 7.803720102857406, 1.8453345716283722, 'HP:0033353', 'Abnormal blood vessel morphology'),
(290360, 'HP:0031014', 'Arteria lusoria', 'XPO:0102709', 'abnormal ventral abdominal vein morphology', 0.43636363636363634, 7.803720102857406, 1.8453345716283722, 'HP:0033353', 'Abnormal blood vessel morphology'),
(290361, 'HP:0031014', 'Arteria lusoria', 'XPO:0128534', 'decreased size of the vascular plexus', 0.42592592592592593, 6.65602285090012, 1.683737715843461, 'HP:0025015', 'Abnormal vascular morphology'),
(290362, 'HP:0031014', 'Arteria lusoria', 'XPO:0130399', 'increased size of the dorsal longitudinal anastomosing vessel - left branch', 0.4107142857142857, 6.65602285090012, 1.6533976142795799, 'HP:0025015', 'Abnormal vascular morphology'),
(290363, 'HP:0031014', 'Arteria lusoria', 'XPO:0139723', 'abnormally necrotic blood vessel', 0.4791666666666667, 6.65602285090012, 1.7858735349186892, 'HP:0025015', 'Abnormal vascular morphology'),
(290364, 'HP:0031014', 'Arteria lusoria', 'XPO:0141328', 'edematous circulatory system', 0.4523809523809524, 5.9590888072311134, 1.6418825384106759, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(290365, 'HP:0031014', 'Arteria lusoria', 'XPO:0101919', 'abnormal heart primordium morphology', 0.4318181818181818, 5.9590888072311134, 1.6041330661860995, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(290366, 'HP:0031014', 'Arteria lusoria', 'XPO:0102554', 'abnormal lymph vessel morphology', 0.45098039215686275, 6.65602285090012, 1.732551816109399, 'HP:0025015', 'Abnormal vascular morphology'),
(290367, 'HP:0031014', 'Arteria lusoria', 'XPO:0102575', 'abnormal caudal vein morphology', 0.41379310344827586, 7.803720102857406, 1.7969767833233308, 'HP:0033353', 'Abnormal blood vessel morphology'),
(290368, 'HP:0031014', 'Arteria lusoria', 'XPO:0101900', 'abnormal circulatory system morphology', 0.48717948717948717, 5.9590888072311134, 1.7038620334885908, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(290369, 'HP:0031014', 'Arteria lusoria', 'XPO:0140666', 'abnormally necrotic occipitovertebral artery', 0.4107142857142857, 6.65602285090012, 1.6533976142795799, 'HP:0025015', 'Abnormal vascular morphology'),
(290370, 'HP:0031014', 'Arteria lusoria', 'XPO:0102962', 'abnormal postcaval vein morphology', 0.43636363636363634, 7.803720102857406, 1.8453345716283722, 'HP:0033353', 'Abnormal blood vessel morphology'),
(290371, 'HP:0031014', 'Arteria lusoria', 'XPO:0101638', 'abnormal anatomical structure morphology', 0.41935483870967744, 2.786899518863159, 1.0810641970914296, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(290372, 'HP:0031014', 'Arteria lusoria', 'XPO:0130141', 'increased size of the Jacobsons vein', 0.4067796610169492, 7.803720102857406, 1.7816830857679173, 'HP:0033353', 'Abnormal blood vessel morphology'),
(290373, 'HP:0031014', 'Arteria lusoria', 'XPO:0129377', 'decreased size of the dorsal longitudinal anastomosing vessel - right branch', 0.4107142857142857, 6.65602285090012, 1.6533976142795799, 'HP:0025015', 'Abnormal vascular morphology'),
(290374, 'HP:0031014', 'Arteria lusoria', 'XPO:0103217', 'abnormal dorsal longitudinal anastomosing vessel - right branch morphology', 0.48936170212765956, 6.65602285090012, 1.8047721938563548, 'HP:0025015', 'Abnormal vascular morphology'),
(290375, 'HP:0031014', 'Arteria lusoria', 'XPO:0101685', 'abnormal head vasculature morphology', 0.4423076923076923, 6.65602285090012, 1.7158117924553669, 'HP:0025015', 'Abnormal vascular morphology'),
(290376, 'HP:0031014', 'Arteria lusoria', 'XPO:0139828', 'abnormally necrotic paired dorsal aorta', 0.40625, 8.750570396338642, 1.8854493426004777, 'HP:0011004', 'Abnormal systemic arterial morphology'),
(290377, 'HP:0031014', 'Arteria lusoria', 'XPO:0102136', 'abnormal renal artery morphology', 0.40350877192982454, 6.65602285090012, 1.6388299504535415, 'HP:0025015', 'Abnormal vascular morphology'),
(290378, 'HP:0031014', 'Arteria lusoria', 'XPO:0128474', 'decreased size of the ischiadic vein', 0.4067796610169492, 7.803720102857406, 1.7816830857679173, 'HP:0033353', 'Abnormal blood vessel morphology'),
(290379, 'HP:0031014', 'Arteria lusoria', 'XPO:0102802', 'abnormal arteria subclavia morphology', 0.4107142857142857, 6.65602285090012, 1.6533976142795799, 'HP:0025015', 'Abnormal vascular morphology'),
(290380, 'HP:0031014', 'Arteria lusoria', 'XPO:0101840', 'abnormal ventral aorta morphology', 0.4262295081967213, 8.750570396338642, 1.93125640878476, 'HP:0011004', 'Abnormal systemic arterial morphology'),
(290381, 'HP:0031014', 'Arteria lusoria', 'XPO:0102570', 'abnormal duct of Cuvier morphology', 0.41379310344827586, 7.803720102857406, 1.7969767833233308, 'HP:0033353', 'Abnormal blood vessel morphology'),
(290382, 'HP:0031014', 'Arteria lusoria', 'XPO:0139990', 'abnormally necrotic cardiovascular system', 0.4222222222222222, 5.9590888072311134, 1.5862092291399303, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(290383, 'HP:0031014', 'Arteria lusoria', 'XPO:0102683', 'abnormal intersomitic vein morphology', 0.45098039215686275, 6.65602285090012, 1.732551816109399, 'HP:0025015', 'Abnormal vascular morphology'),
(290384, 'HP:0031014', 'Arteria lusoria', 'XPO:0102875', 'abnormal vertebral artery morphology', 0.46938775510204084, 6.65602285090012, 1.7675563990696006, 'HP:0025015', 'Abnormal vascular morphology'),
(290385, 'HP:0031014', 'Arteria lusoria', 'XPO:0129512', 'increased size of the cardiovascular system', 0.40425531914893614, 5.9590888072311134, 1.552093214856655, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(290386, 'HP:0031014', 'Arteria lusoria', 'XPO:0141260', 'abnormally necrotic dorsal longitudinal anastomosing vessel - left branch', 0.42592592592592593, 6.65602285090012, 1.683737715843461, 'HP:0025015', 'Abnormal vascular morphology'),
(290387, 'HP:0031014', 'Arteria lusoria', 'XPO:0100792', 'abnormal capillary', 0.41025641025641024, 5.809304221129108, 1.5437954190396599, 'UPHENO:0002678', 'abnormal vasculature'),
(290388, 'HP:0031014', 'Arteria lusoria', 'XPO:0140207', 'abnormally necrotic branchial vein', 0.42105263157894735, 7.803720102857406, 1.8126712016837594, 'HP:0033353', 'Abnormal blood vessel morphology'),
(290389, 'HP:0031014', 'Arteria lusoria', 'XPO:0101845', 'abnormal right channel of ventral aorta morphology', 0.42592592592592593, 6.65602285090012, 1.683737715843461, 'HP:0025015', 'Abnormal vascular morphology'),
(290390, 'HP:0031014', 'Arteria lusoria', 'XPO:0130485', 'increased size of the branchial vein', 0.4067796610169492, 7.803720102857406, 1.7816830857679173, 'HP:0033353', 'Abnormal blood vessel morphology'),
(290391, 'HP:0031014', 'Arteria lusoria', 'XPO:0102935', 'abnormal bulbous arteriosis morphology', 0.4523809523809524, 5.9590888072311134, 1.6418825384106759, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(290392, 'HP:0031014', 'Arteria lusoria', 'XPO:0140800', 'abnormally necrotic larval aorta', 0.4107142857142857, 6.65602285090012, 1.6533976142795799, 'HP:0025015', 'Abnormal vascular morphology'),
(290393, 'HP:0031014', 'Arteria lusoria', 'XPO:0129510', 'increased size of the blood vessel', 0.46, 6.65602285090012, 1.7497915622765061, 'HP:0025015', 'Abnormal vascular morphology'),
(290394, 'HP:0031014', 'Arteria lusoria', 'XPO:0101583', 'abnormal truncus arteriosus', 0.41025641025641024, 5.809304221129108, 1.5437954190396599, 'UPHENO:0002678', 'abnormal vasculature'),
(290395, 'HP:0031014', 'Arteria lusoria', 'XPO:0128481', 'decreased size of the circulatory system', 0.40425531914893614, 5.9590888072311134, 1.552093214856655, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(290396, 'HP:0031014', 'Arteria lusoria', 'XPO:0140420', 'abnormally necrotic bulbous arteriosis', 0.40425531914893614, 5.9590888072311134, 1.552093214856655, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(290397, 'HP:0031014', 'Arteria lusoria', 'XPO:0141079', 'abnormally necrotic ischiadic vein', 0.42105263157894735, 7.803720102857406, 1.8126712016837594, 'HP:0033353', 'Abnormal blood vessel morphology'),
(290398, 'HP:0031014', 'Arteria lusoria', 'XPO:0102838', 'abnormal ischiadic vein morphology', 0.48, 7.803720102857406, 1.9354032265581131, 'HP:0033353', 'Abnormal blood vessel morphology'),
(290399, 'HP:0031014', 'Arteria lusoria', 'XPO:0102113', 'abnormal anatomical line morphology', 0.41935483870967744, 2.786899518863159, 1.0810641970914296, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(290400, 'HP:0031014', 'Arteria lusoria', 'XPO:0130400', 'increased size of the dorsal longitudinal anastomosing vessel', 0.4339622641509434, 6.65602285090012, 1.6995478065112006, 'HP:0025015', 'Abnormal vascular morphology'),
(290401, 'HP:0031014', 'Arteria lusoria', 'XPO:0128099', 'decreased size of the artery', 0.41818181818181815, 6.65602285090012, 1.6683607936082474, 'HP:0025015', 'Abnormal vascular morphology'),
(290402, 'HP:0031014', 'Arteria lusoria', 'XPO:0101686', 'abnormal blood vessel morphology', 0.5348837209302325, 6.65602285090012, 1.8868487668825265, 'HP:0025015', 'Abnormal vascular morphology'),
(290403, 'HP:0031014', 'Arteria lusoria', 'XPO:0102311', 'abnormal left channel of ventral aorta morphology', 0.42592592592592593, 6.65602285090012, 1.683737715843461, 'HP:0025015', 'Abnormal vascular morphology'),
(290404, 'HP:0031014', 'Arteria lusoria', 'XPO:0102619', 'abnormal larval aorta morphology', 0.46938775510204084, 6.65602285090012, 1.7675563990696006, 'HP:0025015', 'Abnormal vascular morphology'),
(290405, 'HP:0031014', 'Arteria lusoria', 'XPO:0102412', 'abnormal vascular plexus morphology', 0.5, 6.65602285090012, 1.8242838116504954, 'HP:0025015', 'Abnormal vascular morphology'),
(290406, 'HP:0031014', 'Arteria lusoria', 'XPO:0128921', 'decreased size of the dorsal longitudinal anastomosing vessel - left branch', 0.4107142857142857, 6.65602285090012, 1.6533976142795799, 'HP:0025015', 'Abnormal vascular morphology'),
(290407, 'HP:0031014', 'Arteria lusoria', 'XPO:0102251', 'abnormal interrenal vein morphology', 0.43636363636363634, 7.803720102857406, 1.8453345716283722, 'HP:0033353', 'Abnormal blood vessel morphology'),
(290408, 'HP:0031014', 'Arteria lusoria', 'XPO:0102612', 'abnormal dorsal longitudinal anastomosing vessel - left branch morphology', 0.48936170212765956, 6.65602285090012, 1.8047721938563548, 'HP:0025015', 'Abnormal vascular morphology'),
(290409, 'HP:0031014', 'Arteria lusoria', 'XPO:0101955', 'abnormal intersomitic artery morphology', 0.4107142857142857, 6.65602285090012, 1.6533976142795799, 'HP:0025015', 'Abnormal vascular morphology'),
(290410, 'HP:0031014', 'Arteria lusoria', 'XPO:0102291', 'abnormal anterior cardinal vein morphology', 0.43636363636363634, 7.803720102857406, 1.8453345716283722, 'HP:0033353', 'Abnormal blood vessel morphology'),
(290411, 'HP:0031014', 'Arteria lusoria', 'XPO:0129296', 'decreased size of the truncus arteriosus', 0.4339622641509434, 6.65602285090012, 1.6995478065112006, 'HP:0025015', 'Abnormal vascular morphology'),
(290412, 'HP:0031014', 'Arteria lusoria', 'XPO:0139826', 'abnormally necrotic cardinal vein', 0.4067796610169492, 7.803720102857406, 1.7816830857679173, 'HP:0033353', 'Abnormal blood vessel morphology'),
(290413, 'HP:0031014', 'Arteria lusoria', 'XPO:0101774', 'abnormal paired dorsal aorta morphology', 0.4642857142857143, 8.750570396338642, 2.015630131465471, 'HP:0011004', 'Abnormal systemic arterial morphology'),
(290414, 'HP:0031014', 'Arteria lusoria', 'XPO:0103091', 'abnormal arteria iliaca communis morphology', 0.4406779661016949, 8.750570396338642, 1.9637167729813316, 'HP:0011004', 'Abnormal systemic arterial morphology'),
(290415, 'HP:0031014', 'Arteria lusoria', 'XPO:0102355', 'abnormal lateral postcardinal vein morphology', 0.43636363636363634, 7.803720102857406, 1.8453345716283722, 'HP:0033353', 'Abnormal blood vessel morphology'),
(290416, 'HP:0031014', 'Arteria lusoria', 'XPO:0102532', 'abnormal angioblast morphology', 0.4318181818181818, 5.9590888072311134, 1.6041330661860995, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(290417, 'HP:0031014', 'Arteria lusoria', 'XPO:0101916', 'abnormal tail vasculature morphology', 0.45098039215686275, 6.65602285090012, 1.732551816109399, 'HP:0025015', 'Abnormal vascular morphology'),
(290418, 'HP:0031014', 'Arteria lusoria', 'XPO:0100076', 'abnormal artery', 0.41025641025641024, 5.809304221129108, 1.5437954190396599, 'UPHENO:0002678', 'abnormal vasculature'),
(290419, 'HP:0031014', 'Arteria lusoria', 'XPO:0129573', 'increased size of the aorta', 0.4126984126984127, 8.750570396338642, 1.900354312430889, 'HP:0011004', 'Abnormal systemic arterial morphology'),
(290420, 'HP:0031014', 'Arteria lusoria', 'XPO:0102800', 'abnormal circulating cell morphology', 0.4318181818181818, 5.9590888072311134, 1.6041330661860995, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(290421, 'HP:0031014', 'Arteria lusoria', 'XPO:0101780', 'abnormal arteria mesenterica posterior morphology', 0.4262295081967213, 8.750570396338642, 1.93125640878476, 'HP:0011004', 'Abnormal systemic arterial morphology'),
(290422, 'HP:0031014', 'Arteria lusoria', 'XPO:0140152', 'abnormally necrotic capillary', 0.4444444444444444, 7.803720102857406, 1.8623426230729947, 'HP:0033353', 'Abnormal blood vessel morphology'),
(290423, 'HP:0031014', 'Arteria lusoria', 'XPO:0102904', 'abnormal lateral abdominal vein morphology', 0.43636363636363634, 7.803720102857406, 1.8453345716283722, 'HP:0033353', 'Abnormal blood vessel morphology'),
(290424, 'HP:0031014', 'Arteria lusoria', 'XPO:0101154', 'abnormal external carotid artery', 0.4642857142857143, 8.750570396338642, 2.015630131465471, 'HP:0011004', 'Abnormal systemic arterial morphology'),
(290425, 'HP:0031014', 'Arteria lusoria', 'XPO:0141249', 'abnormally necrotic dorsal longitudinal anastomosing vessel - right branch', 0.42592592592592593, 6.65602285090012, 1.683737715843461, 'HP:0025015', 'Abnormal vascular morphology'),
(290426, 'HP:0031014', 'Arteria lusoria', 'XPO:0101713', 'abnormal anatomical entity in vitro morphology', 0.41935483870967744, 2.786899518863159, 1.0810641970914296, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(290427, 'HP:0031014', 'Arteria lusoria', 'XPO:0102849', 'abnormal tail vein morphology', 0.42857142857142855, 7.803720102857406, 1.828784151465988, 'HP:0033353', 'Abnormal blood vessel morphology'),
(290428, 'HP:0031014', 'Arteria lusoria', 'XPO:0102166', 'abnormal medial abdominal vein morphology', 0.43636363636363634, 7.803720102857406, 1.8453345716283722, 'HP:0033353', 'Abnormal blood vessel morphology'),
(290429, 'HP:0031014', 'Arteria lusoria', 'XPO:0102565', 'abnormal branchial vein morphology', 0.48, 7.803720102857406, 1.9354032265581131, 'HP:0033353', 'Abnormal blood vessel morphology'),
(290430, 'HP:0100512', 'Decreased circulating vitamin D concentration', 'XPO:0141792', 'abnormal small molecule metabolic process', 0.45161290322580644, 8.366559792680423, 1.943822614845477, 'UPHENO:0049618', 'abnormal small molecule metabolic process'),
(290431, 'HP:0100512', 'Decreased circulating vitamin D concentration', 'XPO:0141787', 'abnormal hormone metabolic process', 0.40625, 6.913987275905781, 1.6759496802818168, 'UPHENO:0049873', 'abnormal metabolic process'),
(290432, 'HP:0100512', 'Decreased circulating vitamin D concentration', 'XPO:0141872', 'abnormal cholesterol metabolic process', 0.45714285714285713, 9.91284182523752, 2.1287519428985364, 'UPHENO:0049723', 'abnormal lipid metabolic process'),
(290433, 'HP:0100512', 'Decreased circulating vitamin D concentration', 'XPO:0141786', 'abnormal pigment metabolic process', 0.40625, 6.913987275905781, 1.6759496802818168, 'UPHENO:0049873', 'abnormal metabolic process'),
(290434, 'HP:0100512', 'Decreased circulating vitamin D concentration', 'XPO:0141794', 'abnormal prosthetic group metabolic process', 0.40625, 6.913987275905781, 1.6759496802818168, 'UPHENO:0049873', 'abnormal metabolic process'),
(290435, 'HP:0100512', 'Decreased circulating vitamin D concentration', 'XPO:0141778', 'abnormal biosynthetic process', 0.40625, 6.913987275905781, 1.6759496802818168, 'UPHENO:0049873', 'abnormal metabolic process'),
(290436, 'HP:0100512', 'Decreased circulating vitamin D concentration', 'XPO:0141904', 'abnormal glucosamine metabolic process', 0.40625, 6.913987275905781, 1.6759496802818168, 'UPHENO:0049873', 'abnormal metabolic process'),
(290437, 'HP:0100512', 'Decreased circulating vitamin D concentration', 'XPO:0141777', 'abnormal catabolic process', 0.40625, 6.913987275905781, 1.6759496802818168, 'UPHENO:0049873', 'abnormal metabolic process'),
(290438, 'HP:0100512', 'Decreased circulating vitamin D concentration', 'XPO:0141791', 'abnormal primary metabolic process', 0.45161290322580644, 7.5690956201444655, 1.8488648538514594, 'UPHENO:0050116', 'abnormal primary metabolic process'),
(290439, 'HP:0100512', 'Decreased circulating vitamin D concentration', 'XPO:0141898', 'abnormal maltose metabolic process', 0.4117647058823529, 7.5690956201444655, 1.7654139548061218, 'UPHENO:0050116', 'abnormal primary metabolic process'),
(290440, 'HP:0100512', 'Decreased circulating vitamin D concentration', 'XPO:0141852', 'abnormal glucose metabolic process', 0.42857142857142855, 8.366559792680423, 1.8935861434266263, 'UPHENO:0049618', 'abnormal small molecule metabolic process'),
(290441, 'HP:0100512', 'Decreased circulating vitamin D concentration', 'XPO:0141798', 'abnormal lipid metabolic process', 0.46875, 9.91284182523752, 2.1556077114308363, 'UPHENO:0049723', 'abnormal lipid metabolic process'),
(290442, 'HP:0100512', 'Decreased circulating vitamin D concentration', 'XPO:0141856', 'abnormal glycerolipid metabolic process', 0.40540540540540543, 9.91284182523752, 2.0046744520944233, 'UPHENO:0049723', 'abnormal lipid metabolic process'),
(290443, 'HP:0100512', 'Decreased circulating vitamin D concentration', 'XPO:0141783', 'abnormal collagen metabolic process', 0.40625, 6.913987275905781, 1.6759496802818168, 'UPHENO:0049873', 'abnormal metabolic process'),
(290444, 'HP:0100512', 'Decreased circulating vitamin D concentration', 'XPO:0141775', 'abnormal nitrogen compound metabolic process', 0.40625, 6.913987275905781, 1.6759496802818168, 'UPHENO:0049873', 'abnormal metabolic process'),
(290445, 'HP:0100512', 'Decreased circulating vitamin D concentration', 'XPO:0141776', 'abnormal metabolic process', 0.43333333333333335, 6.913987275905781, 1.730913386883499, 'UPHENO:0049873', 'abnormal metabolic process'),
(290446, 'HP:0100512', 'Decreased circulating vitamin D concentration', 'XPO:0141796', 'abnormal demethylation', 0.40625, 6.913987275905781, 1.6759496802818168, 'UPHENO:0049873', 'abnormal metabolic process'),
(290447, 'HP:0100512', 'Decreased circulating vitamin D concentration', 'XPO:0141892', 'abnormal inositol metabolic process', 0.42424242424242425, 8.366559792680423, 1.8839983038782007, 'UPHENO:0049618', 'abnormal small molecule metabolic process'),
(290448, 'HP:0100512', 'Decreased circulating vitamin D concentration', 'XPO:0141900', 'abnormal mannose metabolic process', 0.42857142857142855, 8.366559792680423, 1.8935861434266263, 'UPHENO:0049618', 'abnormal small molecule metabolic process'),
(290449, 'HP:0100512', 'Decreased circulating vitamin D concentration', 'XPO:0141795', 'abnormal glycosylation', 0.42424242424242425, 9.417633977274692, 1.9988396306724656, 'HP:0032245', 'Abnormal metabolism'),
(290450, 'HP:0100512', 'Decreased circulating vitamin D concentration', 'XPO:0141910', 'abnormal D-ribose metabolic process', 0.42857142857142855, 8.366559792680423, 1.8935861434266263, 'UPHENO:0049618', 'abnormal small molecule metabolic process'),
(290451, 'HP:0100512', 'Decreased circulating vitamin D concentration', 'XPO:0141797', 'abnormal hydrogen metabolic process', 0.40625, 6.913987275905781, 1.6759496802818168, 'UPHENO:0049873', 'abnormal metabolic process'),
(290452, 'HP:0100512', 'Decreased circulating vitamin D concentration', 'XPO:0141781', 'abnormal secondary metabolic process', 0.40625, 6.913987275905781, 1.6759496802818168, 'UPHENO:0049873', 'abnormal metabolic process'),
(290453, 'HP:0100512', 'Decreased circulating vitamin D concentration', 'XPO:0141881', 'abnormal fructose metabolic process', 0.42857142857142855, 8.366559792680423, 1.8935861434266263, 'UPHENO:0049618', 'abnormal small molecule metabolic process'),
(290454, 'HP:0100512', 'Decreased circulating vitamin D concentration', 'XPO:0141883', 'abnormal glycerol metabolic process', 0.42857142857142855, 8.366559792680423, 1.8935861434266263, 'UPHENO:0049618', 'abnormal small molecule metabolic process'),
(290455, 'HP:0100512', 'Decreased circulating vitamin D concentration', 'XPO:0141782', 'abnormal methylation', 0.40625, 6.913987275905781, 1.6759496802818168, 'UPHENO:0049873', 'abnormal metabolic process'),
(290456, 'HP:0100512', 'Decreased circulating vitamin D concentration', 'XPO:0141850', 'abnormal galactose metabolic process', 0.42857142857142855, 8.366559792680423, 1.8935861434266263, 'UPHENO:0049618', 'abnormal small molecule metabolic process'),
(290457, 'HP:0030363', 'Primary Caesarian section', 'XPO:0101004', 'abnormal acid secreting cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(290458, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100151', 'abnormal primordium', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290459, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100258', 'abnormal organ part', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290460, 'HP:0030363', 'Primary Caesarian section', 'XPO:0141794', 'abnormal prosthetic group metabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(290461, 'HP:0030363', 'Primary Caesarian section', 'XPO:0141787', 'abnormal hormone metabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(290462, 'HP:0030363', 'Primary Caesarian section', 'XPO:0101389', 'abnormal wedge region', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(290463, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100023', 'abnormal mesenchyme', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290464, 'HP:0030363', 'Primary Caesarian section', 'XPO:0101302', 'abnormal subcortical cytoplasm', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(290465, 'HP:0030363', 'Primary Caesarian section', 'XPO:0101547', 'abnormal lampbrush chromosome', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(290466, 'HP:0030363', 'Primary Caesarian section', 'XPO:0115508', 'abnormally peramorphic growth of whole organism', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290467, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100667', 'abnormal vegetal yolk mass', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290468, 'HP:0030363', 'Primary Caesarian section', 'XPO:0101448', 'abnormal myelin accumulating cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(290469, 'HP:0030363', 'Primary Caesarian section', 'XPO:0101061', 'abnormal plasma membrane', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(290470, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100688', 'abnormal adipose tissue', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(290471, 'HP:0030363', 'Primary Caesarian section', 'XPO:0101378', 'abnormal blastomere D1', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(290472, 'HP:0030363', 'Primary Caesarian section', 'XPO:0131723', 'abnormal pathway-restricted SMAD protein phosphorylation', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(290473, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100912', 'abnormal trabecula', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290474, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100372', 'abnormal hematological system', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(290475, 'HP:0030363', 'Primary Caesarian section', 'XPO:0101157', 'abnormal female organism', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290476, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100721', 'abnormal centromere', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(290477, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100856', 'abnormal simple organ', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290478, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100599', 'abnormal adult immune system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(290479, 'HP:0030363', 'Primary Caesarian section', 'XPO:0101132', 'abnormal apoptotic cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(290480, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100503', 'abnormal blastomere D2', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(290481, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100084', 'abnormal anatomical group', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290482, 'HP:0030363', 'Primary Caesarian section', 'XPO:0141267', 'abnormal resting posture', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(290483, 'HP:0030363', 'Primary Caesarian section', 'XPO:0101311', 'abnormal bottle cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(290484, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100009', 'abnormal multi-tissue structure', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290485, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100724', 'abnormal kinetochore', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(290486, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100915', 'abnormal dermal system', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290487, 'HP:0030363', 'Primary Caesarian section', 'XPO:0101472', 'abnormal zygote cortex', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(290488, 'HP:0030363', 'Primary Caesarian section', 'XPO:0141841', 'abnormality of whole organism mass', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(290489, 'HP:0030363', 'Primary Caesarian section', 'XPO:0141265', 'abnormal escape behavior', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(290490, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100501', 'abnormal urogenital system', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(290491, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100515', 'abnormal somatic stem cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(290492, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100415', 'abnormal secretory epithelial cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(290493, 'HP:0030363', 'Primary Caesarian section', 'XPO:0107270', 'abnormal proximal-distal axis', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290494, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100010', 'abnormal multicellular anatomical structure', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290495, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100417', 'abnormal dense regular connective tissue', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(290496, 'HP:0030363', 'Primary Caesarian section', 'XPO:0141271', 'increased surface breathing', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(290497, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100363', 'abnormal cardiovascular system', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290498, 'HP:0030363', 'Primary Caesarian section', 'XPO:0101535', 'abnormal absorptive cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(290499, 'HP:0030363', 'Primary Caesarian section', 'XPO:0107258', 'abnormal anatomical axis', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290500, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100394', 'abnormal marginal zone', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290501, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100273', 'abnormal visual system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(290502, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100887', 'abnormal right-dorsal blastomere', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(290503, 'HP:0030363', 'Primary Caesarian section', 'XPO:0107339', 'abnormal yolk platelet', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(290504, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100477', 'abnormal pericyte', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(290505, 'HP:0030363', 'Primary Caesarian section', 'XPO:0101264', 'abnormal mitotic spindle', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(290506, 'HP:0030363', 'Primary Caesarian section', 'XPO:0107259', 'abnormal animal-vegetal axis', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290507, 'HP:0030363', 'Primary Caesarian section', 'XPO:0101333', 'abnormal barrier epithelial cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(290508, 'HP:0030363', 'Primary Caesarian section', 'XPO:0141315', 'abnormal anatomical region', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290509, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100573', 'abnormal extraembryonic structure', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290510, 'HP:0030363', 'Primary Caesarian section', 'XPO:0101570', 'abnormal forelimb region', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290511, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100791', 'abnormal multiciliated cell precursor', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(290512, 'HP:0030363', 'Primary Caesarian section', 'XPO:0116494', 'absent biological process', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(290513, 'HP:0030363', 'Primary Caesarian section', 'XPO:0107268', 'abnormal left side', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290514, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100427', 'abnormal olfactory system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(290515, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100231', 'abnormal compound organ', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290516, 'HP:0030363', 'Primary Caesarian section', 'XPO:0141266', 'abnormal surface breathing', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(290517, 'HP:0030363', 'Primary Caesarian section', 'XPO:0107278', 'abnormal medial region', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290518, 'HP:0030363', 'Primary Caesarian section', 'XPO:0101136', 'abnormal ooplasm', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(290519, 'HP:0030363', 'Primary Caesarian section', 'XPO:0101463', 'abnormal right-ventral blastomere', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(290520, 'HP:0030363', 'Primary Caesarian section', 'XPO:0101071', 'abnormal endoplasmic reticulum', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(290521, 'HP:0030363', 'Primary Caesarian section', 'XPO:0107284', 'abnormal migrating myoblast', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(290522, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100643', 'abnormal thoracic region', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290523, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100070', 'abnormal anatomical system', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290524, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100186', 'abnormal uveal tract', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290525, 'HP:0030363', 'Primary Caesarian section', 'XPO:0101168', 'abnormal circulating cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(290526, 'HP:0030363', 'Primary Caesarian section', 'XPO:0101513', 'abnormal basal body', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(290527, 'HP:0030363', 'Primary Caesarian section', 'XPO:0141792', 'abnormal small molecule metabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(290528, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100025', 'abnormal oocyte', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(290529, 'HP:0030363', 'Primary Caesarian section', 'XPO:0101467', 'abnormal alkali secreting cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(290530, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100549', 'abnormal mitotic cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(290531, 'HP:0030363', 'Primary Caesarian section', 'XPO:0131687', 'abnormal astral microtubule', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(290532, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100004', 'abnormal cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(290533, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100551', 'abnormal oocyte cortex', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(290534, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100715', 'abnormal ciliated cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(290535, 'HP:0030363', 'Primary Caesarian section', 'XPO:0101575', 'abnormal vitelline membrane', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(290536, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100638', 'abnormal polar body', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(290537, 'HP:0030363', 'Primary Caesarian section', 'XPO:0141748', 'abnormal gas homeostasis', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(290538, 'HP:0030363', 'Primary Caesarian section', 'XPO:0101326', 'abnormal cementoblast', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(290539, 'HP:0030363', 'Primary Caesarian section', 'XPO:0107273', 'abnormal basal region', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290540, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100511', 'abnormal stylopod', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(290541, 'HP:0030363', 'Primary Caesarian section', 'XPO:0107260', 'abnormal anterior-posterior axis', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290542, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100991', 'abnormal iliac process primordium', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290543, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100762', 'abnormal intersomitic region', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290544, 'HP:0030363', 'Primary Caesarian section', 'XPO:0101176', 'abnormal non-ciliated epithelial cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(290545, 'HP:0030363', 'Primary Caesarian section', 'XPO:0101237', 'abnormal mucus secreting cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(290546, 'HP:0030363', 'Primary Caesarian section', 'XPO:0101373', 'abnormal oxygen accumulating cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(290547, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100282', 'abnormal pelvic girdle primordium', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290548, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100581', 'abnormal immune system', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(290549, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100031', 'abnormal central nervous system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(290550, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100481', 'abnormal anatomical line', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290551, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100704', 'abnormal Merkel cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(290552, 'HP:0030363', 'Primary Caesarian section', 'XPO:0141782', 'abnormal methylation', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(290553, 'HP:0030363', 'Primary Caesarian section', 'XPO:0101110', 'abnormal cell-free extract', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290554, 'HP:0030363', 'Primary Caesarian section', 'XPO:0107271', 'abnormal apical region', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290555, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100265', 'abnormal sensory epithelial cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(290556, 'HP:0030363', 'Primary Caesarian section', 'XPO:0141784', 'abnormal cellular hormone metabolic process', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(290557, 'HP:0030363', 'Primary Caesarian section', 'XPO:0101040', 'abnormal axial mesoderm', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290558, 'HP:0030363', 'Primary Caesarian section', 'XPO:0141781', 'abnormal secondary metabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(290559, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100533', 'abnormal melanoblast', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(290560, 'HP:0030363', 'Primary Caesarian section', 'XPO:0141797', 'abnormal hydrogen metabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(290561, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100289', 'abnormal chondroblast', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(290562, 'HP:0030363', 'Primary Caesarian section', 'XPO:0101078', 'abnormal mucous gland', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290563, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100626', 'abnormal primordial germ cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(290564, 'HP:0030363', 'Primary Caesarian section', 'XPO:0141770', 'abnormal urate homeostasis', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(290565, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100069', 'abnormal urinary system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(290566, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100060', 'abnormal regenerating tissue', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290567, 'HP:0030363', 'Primary Caesarian section', 'XPO:0101569', 'abnormal activin-induced ectoderm', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290568, 'HP:0030363', 'Primary Caesarian section', 'XPO:0101503', 'abnormal organ cortex', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290569, 'HP:0030363', 'Primary Caesarian section', 'XPO:0115391', 'abnormally undifferentiated alimentary system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(290570, 'HP:0030363', 'Primary Caesarian section', 'XPO:0141778', 'abnormal biosynthetic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(290571, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100956', 'abnormal centrosome', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(290572, 'HP:0030363', 'Primary Caesarian section', 'XPO:0131669', 'abnormal Roux spot', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(290573, 'HP:0030363', 'Primary Caesarian section', 'XPO:0101220', 'abnormal centriole', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(290574, 'HP:0030363', 'Primary Caesarian section', 'XPO:0101411', 'abnormal marginal zone (sensu neural)', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290575, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100862', 'abnormal blastomere V1', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(290576, 'HP:0030363', 'Primary Caesarian section', 'XPO:0141745', 'abnormal creatinine homeostasis', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(290577, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100002', 'abnormal head', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(290578, 'HP:0030363', 'Primary Caesarian section', 'XPO:0101366', 'abnormal morula cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(290579, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100162', 'abnormal presumptive rhombomere', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290580, 'HP:0030363', 'Primary Caesarian section', 'XPO:0141786', 'abnormal pigment metabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(290581, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100423', 'abnormal process', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290582, 'HP:0030363', 'Primary Caesarian section', 'XPO:0101519', 'abnormal hypobranchial placode', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290583, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100277', 'abnormal blastocoel', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290584, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100308', 'abnormal early embryonic cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(290585, 'HP:0030363', 'Primary Caesarian section', 'XPO:0101468', 'abnormal stage I oocyte', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(290586, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100917', 'abnormal stage III oocyte', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(290587, 'HP:0030363', 'Primary Caesarian section', 'XPO:0101347', 'abnormal hindlimb region', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290588, 'HP:0030363', 'Primary Caesarian section', 'XPO:0101240', 'abnormal ciliated non-epidermal cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(290589, 'HP:0030363', 'Primary Caesarian section', 'XPO:0141738', 'abnormal carbon dioxide homeostasis', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(290590, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100691', 'abnormal keratin accumulating cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(290591, 'HP:0030363', 'Primary Caesarian section', 'XPO:0101480', 'abnormal stage V oocyte', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(290592, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100784', 'abnormal left blastomere', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(290593, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100114', 'abnormal peripheral nervous system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(290594, 'HP:0030363', 'Primary Caesarian section', 'XPO:0141904', 'abnormal glucosamine metabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(290595, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100135', 'abnormal surface structure', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290596, 'HP:0030363', 'Primary Caesarian section', 'XPO:0131675', 'abnormal spindle microtubule', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(290597, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100557', 'abnormal prime meridian', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290598, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100285', 'abnormal progenitor cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(290599, 'HP:0030363', 'Primary Caesarian section', 'XPO:0115512', 'abnormally semi-erect whole organism', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290600, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100384', 'abnormal amputated tissue', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290601, 'HP:0030363', 'Primary Caesarian section', 'XPO:0142056', 'abnormal main body axis', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290602, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100422', 'abnormal notochord', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(290603, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100976', 'abnormal multiciliated cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(290604, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100232', 'abnormal lymphatic system', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(290605, 'HP:0030363', 'Primary Caesarian section', 'XPO:0107261', 'abnormal dorsal-ventral axis', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290606, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100907', 'abnormal cytoplasm', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(290607, 'HP:0030363', 'Primary Caesarian section', 'XPO:0115509', 'abnormally semi-viable whole organism', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290608, 'HP:0030363', 'Primary Caesarian section', 'XPO:0115758', 'abnormally decreased mobility of melanoblast', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(290609, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100852', 'abnormal interdigital region', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(290610, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100902', 'abnormal spermatocyte', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(290611, 'HP:0030363', 'Primary Caesarian section', 'XPO:0142057', 'abnormal desmosome', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(290612, 'HP:0030363', 'Primary Caesarian section', 'XPO:0141771', 'abnormal urea homeostasis', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(290613, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100337', 'abnormal zygote', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(290614, 'HP:0030363', 'Primary Caesarian section', 'XPO:0107288', 'abnormal larval alimentary system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(290615, 'HP:0030363', 'Primary Caesarian section', 'XPO:0101221', 'abnormal larval immune system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(290616, 'HP:0030363', 'Primary Caesarian section', 'XPO:0101497', 'abnormal ciliary axoneme', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(290617, 'HP:0030363', 'Primary Caesarian section', 'XPO:0131677', 'abnormal actin filament', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(290618, 'HP:0030363', 'Primary Caesarian section', 'XPO:0141263', 'abnormal visually guided collision avoidance behavior', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(290619, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100239', 'abnormal acellular anatomical structure', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290620, 'HP:0030363', 'Primary Caesarian section', 'XPO:0142052', 'abnormal nasal region', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(290621, 'HP:0030363', 'Primary Caesarian section', 'XPO:0107265', 'abnormal posterior side', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290622, 'HP:0030363', 'Primary Caesarian section', 'XPO:0131685', 'abnormal cortical actin cytoskeleton', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(290623, 'HP:0030363', 'Primary Caesarian section', 'XPO:0107263', 'abnormal anatomical side', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290624, 'HP:0030363', 'Primary Caesarian section', 'XPO:0141715', 'abnormal septum', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290625, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100293', 'abnormal duct', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290626, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100587', 'abnormal vestibuloauditory system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(290627, 'HP:0030363', 'Primary Caesarian section', 'XPO:0141796', 'abnormal demethylation', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(290628, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100108', 'abnormal cell part', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(290629, 'HP:0030363', 'Primary Caesarian section', 'XPO:0107253', 'abnormal enteric nervous system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(290630, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100888', 'abnormal microtubule', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(290631, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100640', 'abnormal notochordal sheath', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(290632, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100754', 'abnormal electrically active cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(290633, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100176', 'abnormal stage VI oocyte', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(290634, 'HP:0030363', 'Primary Caesarian section', 'XPO:0101113', 'abnormal stage IV oocyte', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(290635, 'HP:0030363', 'Primary Caesarian section', 'XPO:0107312', 'abnormal filopodium', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(290636, 'HP:0030363', 'Primary Caesarian section', 'XPO:0141743', 'abnormal chemical homeostasis within a tissue', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(290637, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100665', 'abnormal egg jelly', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290638, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100547', 'abnormal blastomere V2', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(290639, 'HP:0030363', 'Primary Caesarian section', 'XPO:0131725', 'abnormal phosphorylation of RNA polymerase II C-terminal domain', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(290640, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100251', 'abnormal proteinaceous extracellular matrix', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290641, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100894', 'abnormal nucleus', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(290642, 'HP:0030363', 'Primary Caesarian section', 'XPO:0107272', 'abnormal axial region', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290643, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100642', 'abnormal gustatory system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(290644, 'HP:0030363', 'Primary Caesarian section', 'XPO:00000000', 'Xenopus phenotype', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(290645, 'HP:0030363', 'Primary Caesarian section', 'XPO:0141772', 'abnormal water homeostasis', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(290646, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100317', 'abnormal respiratory system', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(290647, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100402', 'abnormal zeugopod', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(290648, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100392', 'abnormal cilium', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(290649, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100026', 'abnormal germ cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(290650, 'HP:0030363', 'Primary Caesarian section', 'XPO:0142051', 'abnormal cerebrospinal fluid', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(290651, 'HP:0030363', 'Primary Caesarian section', 'XPO:0101072', 'abnormal mitochondrial cloud', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(290652, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100377', 'abnormal connective tissue', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(290653, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100416', 'abnormal ligament', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(290654, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100172', 'abnormal stem cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(290655, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100610', 'abnormal appendage', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290656, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100745', 'abnormal anterior lymph sac', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(290657, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100339', 'abnormal circumblastoporal collar', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290658, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100152', 'abnormal alimentary system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(290659, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100807', 'abnormal matrix-based tissue', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290660, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100225', 'abnormal endocrine system', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(290661, 'HP:0030363', 'Primary Caesarian section', 'XPO:0131667', 'abnormal actin cytoskeleton', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(290662, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100218', 'abnormal epithelial cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(290663, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100120', 'abnormal genital system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(290664, 'HP:0030363', 'Primary Caesarian section', 'XPO:0107285', 'abnormal flexural organ', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(290665, 'HP:0030363', 'Primary Caesarian section', 'XPO:0101409', 'abnormal perivitelline space', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(290666, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100585', 'abnormal elastica externa', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(290667, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100842', 'abnormal left-dorsal blastomere', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(290668, 'HP:0030363', 'Primary Caesarian section', 'XPO:0141276', 'decreased surface breathing', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(290669, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100781', 'abnormal presumptive ectoderm', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290670, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100653', 'abnormal myoblast', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(290671, 'HP:0030363', 'Primary Caesarian section', 'XPO:0141775', 'abnormal nitrogen compound metabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(290672, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100268', 'abnormal circulatory system', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290673, 'HP:0030363', 'Primary Caesarian section', 'XPO:0101405', 'abnormal ring structure', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(290674, 'HP:0030363', 'Primary Caesarian section', 'XPO:0131666', 'abnormal adherens junction', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(290675, 'HP:0030363', 'Primary Caesarian section', 'XPO:0131691', 'abnormal molecular function', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(290676, 'HP:0030363', 'Primary Caesarian section', 'XPO:0115505', 'dead whole organism', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290677, 'HP:0030363', 'Primary Caesarian section', 'XPO:0101228', 'abnormal mesenchymal stem cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(290678, 'HP:0030363', 'Primary Caesarian section', 'XPO:0101200', 'abnormal joint region', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290679, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100574', 'abnormal gastrula cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(290680, 'HP:0030363', 'Primary Caesarian section', 'XPO:0141777', 'abnormal catabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(290681, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100386', 'abnormal limb', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(290682, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100899', 'abnormal secondary spermatogonium', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(290683, 'HP:0030363', 'Primary Caesarian section', 'XPO:0141714', 'abnormal anterior notochord', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(290684, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100202', 'abnormal embryo', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290685, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100104', 'abnormal embryonic structure', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290686, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100164', 'abnormal neural nucleus', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(290687, 'HP:0030363', 'Primary Caesarian section', 'XPO:0101283', 'abnormal left-ventral blastomere', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(290688, 'HP:0030363', 'Primary Caesarian section', 'XPO:0107267', 'abnormal ventral side', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290689, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100900', 'abnormal angioblast', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(290690, 'HP:0030363', 'Primary Caesarian section', 'XPO:0101461', 'abnormal sperm entry point', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(290691, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100429', 'abnormal spermatid', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(290692, 'HP:0030363', 'Primary Caesarian section', 'XPO:0101174', 'abnormal articular system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(290693, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100192', 'abnormal epithelium', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290694, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100014', 'abnormal tissue', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290695, 'HP:0030363', 'Primary Caesarian section', 'XPO:0141783', 'abnormal collagen metabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(290696, 'HP:0030363', 'Primary Caesarian section', 'XPO:0101109', 'abnormal egg cell-free extract', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290697, 'HP:0030363', 'Primary Caesarian section', 'XPO:0107269', 'abnormal right side', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290698, 'HP:0030363', 'Primary Caesarian section', 'XPO:0141499', 'abnormal tadpole', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290699, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100823', 'abnormal blood', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(290700, 'HP:0030363', 'Primary Caesarian section', 'XPO:0141776', 'abnormal metabolic process', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(290701, 'HP:0030363', 'Primary Caesarian section', 'XPO:0101241', 'abnormal nucleate erythrocyte', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(290702, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100802', 'abnormal exocrine cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(290703, 'HP:0030363', 'Primary Caesarian section', 'XPO:0101362', 'abnormal vegetal cortex', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(290704, 'HP:0030363', 'Primary Caesarian section', 'XPO:0141791', 'abnormal primary metabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(290705, 'HP:0030363', 'Primary Caesarian section', 'XPO:0107276', 'abnormal dorsal region', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290706, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100458', 'abnormal autopod', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(290707, 'HP:0030363', 'Primary Caesarian section', 'XPO:0107264', 'abnormal anterior side', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290708, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100742', 'abnormal musculoskeletal system', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290709, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100437', 'abnormal proepicardium', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(290710, 'HP:0030363', 'Primary Caesarian section', 'XPO:0101451', 'abnormal dorsal lymph space', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(290711, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100006', 'abnormal anatomical structure', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290712, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100989', 'abnormal right blastomere', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(290713, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100786', 'abnormal presumptive axial mesoderm', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290714, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100493', 'abnormal liver and biliary system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(290715, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100728', 'abnormal cell condensation', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290716, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100545', 'abnormal male organism', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290717, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100081', 'abnormal anatomical entity in vitro', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290718, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100913', 'abnormal Brachets cleft', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290719, 'HP:0030363', 'Primary Caesarian section', 'XPO:0141272', 'absent surface breathing', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(290720, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100205', 'abnormal limb segment', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(290721, 'HP:0030363', 'Primary Caesarian section', 'XPO:0101498', 'abnormal stage II oocyte', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(290722, 'HP:0030363', 'Primary Caesarian section', 'XPO:0141264', 'abnormal schooling behavior', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(290723, 'HP:0030363', 'Primary Caesarian section', 'XPO:0101023', 'abnormal ultimobranchial body', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(290724, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100969', 'abnormal disaggregated/reaggregated ectoderm treated with activin', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290725, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100999', 'abnormal serous membrane', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290726, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100307', 'abnormal blastomere', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(290727, 'HP:0030363', 'Primary Caesarian section', 'XPO:0116434', 'abnormal biological process', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(290728, 'HP:0030363', 'Primary Caesarian section', 'XPO:0101074', 'abnormal germinal vesicle', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(290729, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100344', 'abnormal portion of organism substance', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290730, 'HP:0030363', 'Primary Caesarian section', 'XPO:0101406', 'abnormal cleavage furrow', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290731, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100531', 'abnormal proliferative region', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290732, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100674', 'abnormal secondary oogonium', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(290733, 'HP:0030363', 'Primary Caesarian section', 'XPO:0141718', 'abnormal posterior notochord', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(290734, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100032', 'abnormal nervous system', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(290735, 'HP:0030363', 'Primary Caesarian section', 'XPO:0101297', 'abnormal barrier cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(290736, 'HP:0030363', 'Primary Caesarian section', 'XPO:0101435', 'abnormal paracrine cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(290737, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100028', 'abnormal anatomical cluster', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290738, 'HP:0030363', 'Primary Caesarian section', 'XPO:0101212', 'abnormal glomeral mesenchyme', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(290739, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100003', 'abnormal organism subdivision', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290740, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100274', 'abnormal sensory system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(290741, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100546', 'abnormal whole organism', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290742, 'HP:0030363', 'Primary Caesarian section', 'XPO:0107266', 'abnormal dorsal side', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290743, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100465', 'abnormal skeletal system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(290744, 'HP:0030363', 'Primary Caesarian section', 'XPO:0107262', 'abnormal left-right axis', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290745, 'HP:0030363', 'Primary Caesarian section', 'XPO:0101141', 'abnormal Keller explant', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290746, 'HP:0030363', 'Primary Caesarian section', 'XPO:0101096', 'abnormal tendon', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(290747, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100295', 'abnormal extracellular matrix', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290748, 'HP:0030363', 'Primary Caesarian section', 'XPO:0100062', 'abnormal anatomical space', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290749, 'HP:0003609', 'Foam cells with lamellar inclusion bodies', 'XPO:0103217', 'abnormal dorsal longitudinal anastomosing vessel - right branch morphology', 0.4107142857142857, 6.65602285090012, 1.6533976142795799, 'HP:0025015', 'Abnormal vascular morphology'),
(290750, 'HP:0003609', 'Foam cells with lamellar inclusion bodies', 'XPO:0102613', 'abnormal dorsal longitudinal anastomosing vessel morphology', 0.42592592592592593, 6.65602285090012, 1.683737715843461, 'HP:0025015', 'Abnormal vascular morphology'),
(290751, 'HP:0003609', 'Foam cells with lamellar inclusion bodies', 'XPO:0101712', 'abnormal aorta morphology', 0.4126984126984127, 8.750570396338642, 1.900354312430889, 'HP:0011004', 'Abnormal systemic arterial morphology'),
(290752, 'HP:0003609', 'Foam cells with lamellar inclusion bodies', 'XPO:0101708', 'abnormal artery morphology', 0.4107142857142857, 6.65602285090012, 1.6533976142795799, 'HP:0025015', 'Abnormal vascular morphology'),
(290753, 'HP:0003609', 'Foam cells with lamellar inclusion bodies', 'XPO:0101686', 'abnormal blood vessel morphology', 0.4423076923076923, 6.65602285090012, 1.7158117924553669, 'HP:0025015', 'Abnormal vascular morphology'),
(290754, 'HP:0003609', 'Foam cells with lamellar inclusion bodies', 'XPO:0139723', 'abnormally necrotic blood vessel', 0.40350877192982454, 6.65602285090012, 1.6388299504535415, 'HP:0025015', 'Abnormal vascular morphology'),
(290755, 'HP:0003609', 'Foam cells with lamellar inclusion bodies', 'XPO:0102800', 'abnormal circulating cell morphology', 0.4117647058823529, 5.9590888072311134, 1.566442609876385, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(290756, 'HP:0003609', 'Foam cells with lamellar inclusion bodies', 'XPO:0103189', 'abnormal Jacobsons vein morphology', 0.4067796610169492, 7.803720102857406, 1.7816830857679173, 'HP:0033353', 'Abnormal blood vessel morphology'),
(290757, 'HP:0003609', 'Foam cells with lamellar inclusion bodies', 'XPO:0102424', 'abnormal capillary morphology', 0.42105263157894735, 7.803720102857406, 1.8126712016837594, 'HP:0033353', 'Abnormal blood vessel morphology'),
(290758, 'HP:0003609', 'Foam cells with lamellar inclusion bodies', 'XPO:0102838', 'abnormal ischiadic vein morphology', 0.4067796610169492, 7.803720102857406, 1.7816830857679173, 'HP:0033353', 'Abnormal blood vessel morphology'),
(290759, 'HP:0003609', 'Foam cells with lamellar inclusion bodies', 'XPO:0102154', 'abnormal subinterstitial vein morphology', 0.4067796610169492, 7.803720102857406, 1.7816830857679173, 'HP:0033353', 'Abnormal blood vessel morphology'),
(290760, 'HP:0003609', 'Foam cells with lamellar inclusion bodies', 'XPO:0102612', 'abnormal dorsal longitudinal anastomosing vessel - left branch morphology', 0.4107142857142857, 6.65602285090012, 1.6533976142795799, 'HP:0025015', 'Abnormal vascular morphology'),
(290761, 'HP:0003609', 'Foam cells with lamellar inclusion bodies', 'XPO:0103215', 'abnormal truncus arteriosus morphology', 0.42592592592592593, 6.65602285090012, 1.683737715843461, 'HP:0025015', 'Abnormal vascular morphology'),
(290762, 'HP:0003609', 'Foam cells with lamellar inclusion bodies', 'XPO:0102532', 'abnormal angioblast morphology', 0.4117647058823529, 5.9590888072311134, 1.566442609876385, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(290763, 'HP:0003609', 'Foam cells with lamellar inclusion bodies', 'XPO:0102565', 'abnormal branchial vein morphology', 0.4067796610169492, 7.803720102857406, 1.7816830857679173, 'HP:0033353', 'Abnormal blood vessel morphology'),
(290764, 'HP:0003609', 'Foam cells with lamellar inclusion bodies', 'XPO:0101675', 'abnormal vein morphology', 0.42105263157894735, 7.803720102857406, 1.8126712016837594, 'HP:0033353', 'Abnormal blood vessel morphology'),
(290765, 'HP:0003609', 'Foam cells with lamellar inclusion bodies', 'XPO:0102412', 'abnormal vascular plexus morphology', 0.41818181818181815, 6.65602285090012, 1.6683607936082474, 'HP:0025015', 'Abnormal vascular morphology'),
(290766, 'HP:0040334', 'Purulent rhinitis', 'XPO:0101469', 'abnormal medial nasal prominence', 0.46875, 3.868794716113063, 1.346661621632546, 'UPHENO:0002844', 'abnormal head'),
(290767, 'HP:0040334', 'Purulent rhinitis', 'XPO:0131678', 'abnormal intercanthal region', 0.45454545454545453, 3.868794716113063, 1.3261006948111689, 'UPHENO:0002844', 'abnormal head'),
(290768, 'HP:0040334', 'Purulent rhinitis', 'XPO:0101103', 'abnormal pharyngeal mesenchyme', 0.40540540540540543, 3.868794716113063, 1.2523698696136485, 'UPHENO:0002844', 'abnormal head'),
(290769, 'HP:0040334', 'Purulent rhinitis', 'XPO:0100664', 'abnormal periocular region', 0.4838709677419355, 3.868794716113063, 1.3682095757889265, 'UPHENO:0002844', 'abnormal head'),
(290770, 'HP:0040334', 'Purulent rhinitis', 'XPO:0101256', 'abnormal head endoderm', 0.42857142857142855, 3.868794716113063, 1.2876547978142938, 'UPHENO:0002844', 'abnormal head'),
(290771, 'HP:0040334', 'Purulent rhinitis', 'XPO:0100647', 'abnormal mouth', 0.40476190476190477, 5.0624614801082695, 1.4314648271866113, 'UPHENO:0002910', 'abnormal face'),
(290772, 'HP:0040334', 'Purulent rhinitis', 'XPO:0100893', 'abnormal hyoid arch', 0.40540540540540543, 3.868794716113063, 1.2523698696136485, 'UPHENO:0002844', 'abnormal head'),
(290773, 'HP:0040334', 'Purulent rhinitis', 'XPO:0100880', 'abnormal head mesoderm', 0.4166666666666667, 3.868794716113063, 1.2696447528267278, 'UPHENO:0002844', 'abnormal head'),
(290774, 'HP:0040334', 'Purulent rhinitis', 'XPO:0100388', 'abnormal adenohypophyseal placode', 0.40540540540540543, 3.868794716113063, 1.2523698696136485, 'UPHENO:0002844', 'abnormal head'),
(290775, 'HP:0040334', 'Purulent rhinitis', 'XPO:0100078', 'abnormal neurogenic placode', 0.42857142857142855, 3.868794716113063, 1.2876547978142938, 'UPHENO:0002844', 'abnormal head'),
(290776, 'HP:0040334', 'Purulent rhinitis', 'XPO:0100940', 'abnormal hatching gland primordium', 0.45454545454545453, 3.868794716113063, 1.3261006948111689, 'UPHENO:0002844', 'abnormal head'),
(290777, 'HP:0040334', 'Purulent rhinitis', 'XPO:0100727', 'abnormal odontogenic papilla', 0.5, 3.868794716113063, 1.3908261422825396, 'UPHENO:0002844', 'abnormal head'),
(290778, 'HP:0040334', 'Purulent rhinitis', 'XPO:0100594', 'abnormal Jacobsons organ', 0.5428571428571428, 9.116652820832241, 2.224643814802159, 'HP:0000366', 'Abnormality of the nose'),
(290779, 'HP:0040334', 'Purulent rhinitis', 'XPO:0100627', 'abnormal pharyngeal region', 0.5, 3.868794716113063, 1.3908261422825396, 'UPHENO:0002844', 'abnormal head'),
(290780, 'HP:0040334', 'Purulent rhinitis', 'XPO:0101173', 'abnormal retinal layer', 0.40476190476190477, 5.0624614801082695, 1.4314648271866113, 'UPHENO:0002910', 'abnormal face'),
(290781, 'HP:0040334', 'Purulent rhinitis', 'XPO:0100450', 'abnormal circumpharyngeal ridge', 0.45454545454545453, 3.868794716113063, 1.3261006948111689, 'UPHENO:0002844', 'abnormal head'),
(290782, 'HP:0040334', 'Purulent rhinitis', 'XPO:0100359', 'abnormal trigeminal placode', 0.40540540540540543, 3.868794716113063, 1.2523698696136485, 'UPHENO:0002844', 'abnormal head'),
(290783, 'HP:0040334', 'Purulent rhinitis', 'XPO:0103304', 'absent olfactory pit', 0.41304347826086957, 9.116652820832241, 1.9405086939288154, 'HP:0000366', 'Abnormality of the nose'),
(290784, 'HP:0040334', 'Purulent rhinitis', 'XPO:0126822', 'abnormally localised pharyngeal region', 0.40540540540540543, 3.868794716113063, 1.2523698696136485, 'UPHENO:0002844', 'abnormal head'),
(290785, 'HP:0040334', 'Purulent rhinitis', 'XPO:0100687', 'abnormal periotic region', 0.4838709677419355, 3.868794716113063, 1.3682095757889265, 'UPHENO:0002844', 'abnormal head'),
(290786, 'HP:0040334', 'Purulent rhinitis', 'XPO:0127893', 'abnormally localised Jacobsons organ', 0.4318181818181818, 9.116652820832241, 1.9841210762852597, 'HP:0000366', 'Abnormality of the nose'),
(290787, 'HP:0040334', 'Purulent rhinitis', 'XPO:0100389', 'abnormal cranial placode', 0.4411764705882353, 3.868794716113063, 1.306453672460365, 'UPHENO:0002844', 'abnormal head'),
(290788, 'HP:0040334', 'Purulent rhinitis', 'XPO:0131656', 'abnormal periocular mesenchyme', 0.4411764705882353, 3.868794716113063, 1.306453672460365, 'UPHENO:0002844', 'abnormal head'),
(290789, 'HP:0040334', 'Purulent rhinitis', 'XPO:0100374', 'abnormal pharyngeal endoderm', 0.4166666666666667, 3.868794716113063, 1.2696447528267278, 'UPHENO:0002844', 'abnormal head'),
(290790, 'HP:0040334', 'Purulent rhinitis', 'XPO:0100002', 'abnormal head', 0.5172413793103449, 3.868794716113063, 1.4146026704452719, 'UPHENO:0002844', 'abnormal head'),
(290791, 'HP:0040334', 'Purulent rhinitis', 'XPO:0101172', 'abnormal pharyngeal pouch', 0.46875, 3.868794716113063, 1.346661621632546, 'UPHENO:0002844', 'abnormal head'),
(290792, 'HP:0040334', 'Purulent rhinitis', 'XPO:0101102', 'abnormal craniofacial region', 0.46875, 3.868794716113063, 1.346661621632546, 'UPHENO:0002844', 'abnormal head'),
(290793, 'HP:0040334', 'Purulent rhinitis', 'XPO:0100572', 'abnormal branchial arch', 0.40540540540540543, 3.868794716113063, 1.2523698696136485, 'UPHENO:0002844', 'abnormal head'),
(290794, 'HP:0040334', 'Purulent rhinitis', 'XPO:0100625', 'abnormal dorsolateral placode region', 0.4166666666666667, 3.868794716113063, 1.2696447528267278, 'UPHENO:0002844', 'abnormal head'),
(290795, 'HP:0040334', 'Purulent rhinitis', 'XPO:0100591', 'abnormal pharyngeal arch', 0.4166666666666667, 3.868794716113063, 1.2696447528267278, 'UPHENO:0002844', 'abnormal head'),
(290796, 'HP:0040334', 'Purulent rhinitis', 'XPO:0100740', 'abnormal profundal placode', 0.4166666666666667, 3.868794716113063, 1.2696447528267278, 'UPHENO:0002844', 'abnormal head'),
(290797, 'HP:0040334', 'Purulent rhinitis', 'XPO:0127208', 'abnormally localised olfactory pit', 0.4634146341463415, 9.116652820832241, 2.0554294761935243, 'HP:0000366', 'Abnormality of the nose'),
(290798, 'HP:0040334', 'Purulent rhinitis', 'XPO:0115812', 'duplicated head', 0.40540540540540543, 3.868794716113063, 1.2523698696136485, 'UPHENO:0002844', 'abnormal head'),
(290799, 'HP:0040334', 'Purulent rhinitis', 'XPO:0101334', 'abnormal olfactory pit', 0.5588235294117647, 9.116652820832241, 2.2571220848149074, 'HP:0000366', 'Abnormality of the nose'),
(290800, 'HP:0040334', 'Purulent rhinitis', 'XPO:0101289', 'abnormal orbital region', 0.4146341463414634, 5.0624614801082695, 1.4488165495297303, 'UPHENO:0002910', 'abnormal face'),
(290801, 'HP:0040334', 'Purulent rhinitis', 'XPO:0142052', 'abnormal nasal region', 0.5172413793103449, 3.868794716113063, 1.4146026704452719, 'UPHENO:0002844', 'abnormal head'),
(290802, 'HP:0040334', 'Purulent rhinitis', 'XPO:0100420', 'abnormal choana', 0.41304347826086957, 9.116652820832241, 1.9405086939288154, 'HP:0000366', 'Abnormality of the nose'),
(290803, 'HP:0040334', 'Purulent rhinitis', 'XPO:0100451', 'abnormal head mesenchyme', 0.46875, 3.868794716113063, 1.346661621632546, 'UPHENO:0002844', 'abnormal head'),
(290804, 'HP:0040334', 'Purulent rhinitis', 'XPO:0100906', 'abnormal lateral nasal prominence', 0.46875, 3.868794716113063, 1.346661621632546, 'UPHENO:0002844', 'abnormal head'),
(290805, 'HP:0040334', 'Purulent rhinitis', 'XPO:0101483', 'abnormal nostril', 0.4318181818181818, 9.116652820832241, 1.9841210762852597, 'HP:0000366', 'Abnormality of the nose'),
(290806, 'HP:0040334', 'Purulent rhinitis', 'XPO:0131672', 'abnormal non-neurogenic ectodermal placode', 0.42857142857142855, 3.868794716113063, 1.2876547978142938, 'UPHENO:0002844', 'abnormal head'),
(290807, 'HP:0040334', 'Purulent rhinitis', 'XPO:0101402', 'abnormal oropharyngeal papilla', 0.4838709677419355, 3.868794716113063, 1.3682095757889265, 'UPHENO:0002844', 'abnormal head'),
(290808, 'HP:0009518', 'Irregular epiphysis of the middle phalanx of the 2nd finger', 'XPO:0103609', 'abnormally increased number of forelimb digit in the regenerating forelimb', 0.41304347826086957, 7.774297771301195, 1.7919606559559202, 'HP:0005918', 'Abnormal finger phalanx morphology'),
(290809, 'HP:0009518', 'Irregular epiphysis of the middle phalanx of the 2nd finger', 'XPO:0103634', 'abnormally increased number of forelimb digit', 0.4318181818181818, 7.774297771301195, 1.8322344633033256, 'HP:0005918', 'Abnormal finger phalanx morphology'),
(290810, 'HP:0011839', 'Abnormal T cell count', 'XPO:0125284', 'absent thymocyte', 0.6081081081081081, 9.586341000560333, 2.4144423143926907, 'HP:0011839', 'Abnormal T cell count'),
(290811, 'HP:0011839', 'Abnormal T cell count', 'XPO:0102080', 'abnormal thymocyte morphology', 0.45569620253164556, 9.260765128657825, 2.054287103027923, 'HP:0002843', 'Abnormal T cell morphology'),
(290812, 'HP:0011839', 'Abnormal T cell count', 'XPO:0140117', 'abnormally necrotic thymocyte', 0.42857142857142855, 9.260765128657825, 1.9922096628752088, 'HP:0002843', 'Abnormal T cell morphology'),
(290813, 'HP:0011839', 'Abnormal T cell count', 'XPO:0131005', 'abnormally increased number of thymocyte', 0.5421686746987951, 9.586341000560333, 2.2797837168215143, 'HP:0011839', 'Abnormal T cell count'),
(290814, 'HP:0011839', 'Abnormal T cell count', 'XPO:0131221', 'abnormally decreased number of thymocyte', 0.5357142857142857, 9.586341000560333, 2.2661729461205624, 'HP:0011839', 'Abnormal T cell count'),
(290815, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0101497', 'abnormal ciliary axoneme', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(290816, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0107259', 'abnormal animal-vegetal axis', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290817, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0100704', 'abnormal Merkel cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(290818, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0100417', 'abnormal dense regular connective tissue', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(290819, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0100688', 'abnormal adipose tissue', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(290820, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0100894', 'abnormal nucleus', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(290821, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0107253', 'abnormal enteric nervous system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(290822, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0100437', 'abnormal proepicardium', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(290823, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0100754', 'abnormal electrically active cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(290824, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0107278', 'abnormal medial region', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290825, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0100547', 'abnormal blastomere V2', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(290826, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0101240', 'abnormal ciliated non-epidermal cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(290827, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0100724', 'abnormal kinetochore', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(290828, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0100852', 'abnormal interdigital region', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(290829, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0101228', 'abnormal mesenchymal stem cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(290830, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0101480', 'abnormal stage V oocyte', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(290831, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0100976', 'abnormal multiciliated cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(290832, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0101463', 'abnormal right-ventral blastomere', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(290833, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0101448', 'abnormal myelin accumulating cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(290834, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0100218', 'abnormal epithelial cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(290835, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0100581', 'abnormal immune system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(290836, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0100422', 'abnormal notochord', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(290837, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0141745', 'abnormal creatinine homeostasis', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(290838, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0101366', 'abnormal morula cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(290839, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0100549', 'abnormal mitotic cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(290840, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0100009', 'abnormal multi-tissue structure', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290841, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0101435', 'abnormal paracrine cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(290842, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0100028', 'abnormal anatomical cluster', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290843, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0100031', 'abnormal central nervous system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(290844, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0101498', 'abnormal stage II oocyte', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(290845, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0100014', 'abnormal tissue', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290846, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0100239', 'abnormal acellular anatomical structure', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290847, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0101113', 'abnormal stage IV oocyte', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(290848, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0101468', 'abnormal stage I oocyte', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(290849, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0131677', 'abnormal actin filament', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(290850, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0100715', 'abnormal ciliated cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(290851, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0107284', 'abnormal migrating myoblast', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(290852, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0100308', 'abnormal early embryonic cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(290853, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0100902', 'abnormal spermatocyte', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(290854, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0100225', 'abnormal endocrine system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(290855, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0100273', 'abnormal visual system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(290856, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0101241', 'abnormal nucleate erythrocyte', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(290857, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0101004', 'abnormal acid secreting cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(290858, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0100152', 'abnormal alimentary system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(290859, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0100025', 'abnormal oocyte', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(290860, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0141738', 'abnormal carbon dioxide homeostasis', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(290861, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0100515', 'abnormal somatic stem cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(290862, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0101302', 'abnormal subcortical cytoplasm', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(290863, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0100969', 'abnormal disaggregated/reaggregated ectoderm treated with activin', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290864, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0101547', 'abnormal lampbrush chromosome', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(290865, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0101472', 'abnormal zygote cortex', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(290866, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0100232', 'abnormal lymphatic system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(290867, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0100392', 'abnormal cilium', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(290868, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0101132', 'abnormal apoptotic cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(290869, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0100899', 'abnormal secondary spermatogonium', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(290870, 'HP:0032435', 'Neonatal omphalitis', 'XPO:00000000', 'Xenopus phenotype', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(290871, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0100084', 'abnormal anatomical group', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290872, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0101326', 'abnormal cementoblast', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(290873, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0100317', 'abnormal respiratory system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(290874, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0100006', 'abnormal anatomical structure', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290875, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0141265', 'abnormal escape behavior', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(290876, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0107260', 'abnormal anterior-posterior axis', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290877, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0100104', 'abnormal embryonic structure', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290878, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0100533', 'abnormal melanoblast', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(290879, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0100429', 'abnormal spermatid', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(290880, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0131723', 'abnormal pathway-restricted SMAD protein phosphorylation', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(290881, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0131669', 'abnormal Roux spot', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(290882, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0107258', 'abnormal anatomical axis', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290883, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0100585', 'abnormal elastica externa', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(290884, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0100626', 'abnormal primordial germ cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(290885, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0141743', 'abnormal chemical homeostasis within a tissue', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(290886, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0131667', 'abnormal actin cytoskeleton', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(290887, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0100674', 'abnormal secondary oogonium', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(290888, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0107273', 'abnormal basal region', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290889, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0101347', 'abnormal hindlimb region', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290890, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0100842', 'abnormal left-dorsal blastomere', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(290891, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0100784', 'abnormal left blastomere', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(290892, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0100372', 'abnormal hematological system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(290893, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0141267', 'abnormal resting posture', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(290894, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0100289', 'abnormal chondroblast', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(290895, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0100062', 'abnormal anatomical space', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290896, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0100653', 'abnormal myoblast', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(290897, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0100862', 'abnormal blastomere V1', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(290898, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0100503', 'abnormal blastomere D2', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(290899, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0107262', 'abnormal left-right axis', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290900, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0100551', 'abnormal oocyte cortex', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(290901, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0101373', 'abnormal oxygen accumulating cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(290902, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0131687', 'abnormal astral microtubule', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(290903, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0100032', 'abnormal nervous system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(290904, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0115505', 'dead whole organism', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290905, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0141315', 'abnormal anatomical region', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290906, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0100477', 'abnormal pericyte', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(290907, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0101411', 'abnormal marginal zone (sensu neural)', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290908, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0101264', 'abnormal mitotic spindle', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(290909, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0141499', 'abnormal tadpole', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290910, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0100307', 'abnormal blastomere', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(290911, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0101061', 'abnormal plasma membrane', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(290912, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0100599', 'abnormal adult immune system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(290913, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0100665', 'abnormal egg jelly', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290914, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0142057', 'abnormal desmosome', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(290915, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0100274', 'abnormal sensory system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(290916, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0100574', 'abnormal gastrula cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(290917, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0101110', 'abnormal cell-free extract', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290918, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0101221', 'abnormal larval immune system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(290919, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0100691', 'abnormal keratin accumulating cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(290920, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0101569', 'abnormal activin-induced ectoderm', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290921, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0100176', 'abnormal stage VI oocyte', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(290922, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0101467', 'abnormal alkali secreting cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(290923, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0107261', 'abnormal dorsal-ventral axis', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290924, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0141272', 'absent surface breathing', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(290925, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0100587', 'abnormal vestibuloauditory system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(290926, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0141264', 'abnormal schooling behavior', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(290927, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0100802', 'abnormal exocrine cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(290928, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0100337', 'abnormal zygote', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(290929, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0131725', 'abnormal phosphorylation of RNA polymerase II C-terminal domain', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(290930, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0100285', 'abnormal progenitor cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(290931, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0131685', 'abnormal cortical actin cytoskeleton', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(290932, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0100638', 'abnormal polar body', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(290933, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0100907', 'abnormal cytoplasm', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(290934, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0100791', 'abnormal multiciliated cell precursor', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(290935, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0107312', 'abnormal filopodium', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(290936, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0101570', 'abnormal forelimb region', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290937, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0100573', 'abnormal extraembryonic structure', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290938, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0100917', 'abnormal stage III oocyte', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(290939, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0101109', 'abnormal egg cell-free extract', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290940, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0100026', 'abnormal germ cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(290941, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0101513', 'abnormal basal body', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(290942, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0101141', 'abnormal Keller explant', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290943, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0100202', 'abnormal embryo', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290944, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0100465', 'abnormal skeletal system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(290945, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0101136', 'abnormal ooplasm', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(290946, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0100277', 'abnormal blastocoel', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290947, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0100108', 'abnormal cell part', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(290948, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0100386', 'abnormal limb', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(290949, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0100377', 'abnormal connective tissue', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(290950, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0101405', 'abnormal ring structure', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(290951, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0101200', 'abnormal joint region', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290952, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0107270', 'abnormal proximal-distal axis', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290953, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0141770', 'abnormal urate homeostasis', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(290954, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0100545', 'abnormal male organism', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290955, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0141748', 'abnormal gas homeostasis', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(290956, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0100546', 'abnormal whole organism', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290957, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0101451', 'abnormal dorsal lymph space', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(290958, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0101220', 'abnormal centriole', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(290959, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0100643', 'abnormal thoracic region', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290960, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0131666', 'abnormal adherens junction', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(290961, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0101378', 'abnormal blastomere D1', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(290962, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0107263', 'abnormal anatomical side', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290963, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0100004', 'abnormal cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(290964, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0101237', 'abnormal mucus secreting cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(290965, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0107271', 'abnormal apical region', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290966, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0100887', 'abnormal right-dorsal blastomere', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(290967, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0101575', 'abnormal vitelline membrane', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(290968, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0141784', 'abnormal cellular hormone metabolic process', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(290969, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0100070', 'abnormal anatomical system', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290970, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0100728', 'abnormal cell condensation', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290971, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0100295', 'abnormal extracellular matrix', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290972, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0115509', 'abnormally semi-viable whole organism', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290973, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0100501', 'abnormal urogenital system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(290974, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0100344', 'abnormal portion of organism substance', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290975, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0101283', 'abnormal left-ventral blastomere', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(290976, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0100956', 'abnormal centrosome', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(290977, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0101072', 'abnormal mitochondrial cloud', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(290978, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0141263', 'abnormal visually guided collision avoidance behavior', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(290979, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0100003', 'abnormal organism subdivision', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290980, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0101297', 'abnormal barrier cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(290981, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0141771', 'abnormal urea homeostasis', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(290982, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0100172', 'abnormal stem cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(290983, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0100258', 'abnormal organ part', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290984, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0100721', 'abnormal centromere', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(290985, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0131675', 'abnormal spindle microtubule', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(290986, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0100642', 'abnormal gustatory system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(290987, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0107276', 'abnormal dorsal region', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290988, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0100762', 'abnormal intersomitic region', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290989, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0107272', 'abnormal axial region', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290990, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0101157', 'abnormal female organism', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290991, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0100888', 'abnormal microtubule', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(290992, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0115512', 'abnormally semi-erect whole organism', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290993, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0101333', 'abnormal barrier epithelial cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(290994, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0107339', 'abnormal yolk platelet', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(290995, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0100205', 'abnormal limb segment', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(290996, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0100010', 'abnormal multicellular anatomical structure', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290997, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0100081', 'abnormal anatomical entity in vitro', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(290998, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0141772', 'abnormal water homeostasis', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(290999, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0141266', 'abnormal surface breathing', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(291000, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0100989', 'abnormal right blastomere', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(291001, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0101409', 'abnormal perivitelline space', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(291002, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0100423', 'abnormal process', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(291003, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0100427', 'abnormal olfactory system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(291004, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0115508', 'abnormally peramorphic growth of whole organism', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(291005, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0101071', 'abnormal endoplasmic reticulum', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(291006, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0100481', 'abnormal anatomical line', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(291007, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0101389', 'abnormal wedge region', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(291008, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0101311', 'abnormal bottle cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(291009, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0101535', 'abnormal absorptive cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(291010, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0101461', 'abnormal sperm entry point', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(291011, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0141776', 'abnormal metabolic process', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(291012, 'HP:0032435', 'Neonatal omphalitis', 'XPO:0100823', 'abnormal blood', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(291013, 'HP:0033013', 'Abnormal salivary cortisol level', 'XPO:0141852', 'abnormal glucose metabolic process', 0.44, 4.758907843651163, 1.447038165082909, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(291014, 'HP:0033013', 'Abnormal salivary cortisol level', 'XPO:0100070', 'abnormal anatomical system', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(291015, 'HP:0033013', 'Abnormal salivary cortisol level', 'XPO:0131719', 'abnormal activation of meiosis', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(291016, 'HP:0033013', 'Abnormal salivary cortisol level', 'XPO:0100823', 'abnormal blood', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(291017, 'HP:0033013', 'Abnormal salivary cortisol level', 'XPO:0107276', 'abnormal dorsal region', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(291018, 'HP:0033013', 'Abnormal salivary cortisol level', 'XPO:0100842', 'abnormal left-dorsal blastomere', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(291019, 'HP:0033013', 'Abnormal salivary cortisol level', 'XPO:0141600', 'absent metamorphosis', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(291020, 'HP:0033013', 'Abnormal salivary cortisol level', 'XPO:0131669', 'abnormal Roux spot', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(291021, 'HP:0033013', 'Abnormal salivary cortisol level', 'XPO:0100754', 'abnormal electrically active cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(291022, 'HP:0033013', 'Abnormal salivary cortisol level', 'XPO:0101240', 'abnormal ciliated non-epidermal cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(291023, 'HP:0033013', 'Abnormal salivary cortisol level', 'XPO:0100032', 'abnormal nervous system', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(291024, 'HP:0033013', 'Abnormal salivary cortisol level', 'XPO:0100715', 'abnormal ciliated cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(291025, 'HP:0033013', 'Abnormal salivary cortisol level', 'XPO:0141854', 'abnormal glutathione metabolic process', 0.44, 4.758907843651163, 1.447038165082909, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(291026, 'HP:0033013', 'Abnormal salivary cortisol level', 'XPO:0100902', 'abnormal spermatocyte', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(291027, 'HP:0033013', 'Abnormal salivary cortisol level', 'XPO:0128000', 'absent behavior', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(291028, 'HP:0033013', 'Abnormal salivary cortisol level', 'XPO:0100653', 'abnormal myoblast', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(291029, 'HP:0033013', 'Abnormal salivary cortisol level', 'XPO:0141271', 'increased surface breathing', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(291030, 'HP:0033013', 'Abnormal salivary cortisol level', 'XPO:0101109', 'abnormal egg cell-free extract', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(291031, 'HP:0033013', 'Abnormal salivary cortisol level', 'XPO:0141276', 'decreased surface breathing', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(291032, 'HP:0033013', 'Abnormal salivary cortisol level', 'XPO:0100026', 'abnormal germ cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(291033, 'HP:0033013', 'Abnormal salivary cortisol level', 'XPO:0101072', 'abnormal mitochondrial cloud', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(291034, 'HP:0033013', 'Abnormal salivary cortisol level', 'XPO:0100956', 'abnormal centrosome', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(291035, 'HP:0033013', 'Abnormal salivary cortisol level', 'XPO:0133401', 'absent determination of left/right symmetry in lateral plate mesoderm', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(291036, 'HP:0033013', 'Abnormal salivary cortisol level', 'XPO:0141777', 'abnormal catabolic process', 0.55, 4.758907843651163, 1.6178378515809735, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(291037, 'HP:0033013', 'Abnormal salivary cortisol level', 'XPO:0141743', 'abnormal chemical homeostasis within a tissue', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(291038, 'HP:0033013', 'Abnormal salivary cortisol level', 'XPO:0101389', 'abnormal wedge region', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(291039, 'HP:0033013', 'Abnormal salivary cortisol level', 'XPO:0141767', 'abnormal temperature homeostasis', 0.4583333333333333, 4.758907843651163, 1.4768771428276568, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(291040, 'HP:0033013', 'Abnormal salivary cortisol level', 'XPO:0141958', 'absent cilium motility in left-right organizer', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(291041, 'HP:0033013', 'Abnormal salivary cortisol level', 'XPO:0100501', 'abnormal urogenital system', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(291042, 'HP:0033013', 'Abnormal salivary cortisol level', 'XPO:0141920', 'abnormal urea metabolic process', 0.4074074074074074, 4.758907843651163, 1.392413123563799, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(291043, 'HP:0033013', 'Abnormal salivary cortisol level', 'XPO:0116433', 'abnormal axis specification', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(291044, 'HP:0033013', 'Abnormal salivary cortisol level', 'XPO:0101132', 'abnormal apoptotic cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(291045, 'HP:0033013', 'Abnormal salivary cortisol level', 'XPO:0107259', 'abnormal animal-vegetal axis', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(291046, 'HP:0033013', 'Abnormal salivary cortisol level', 'XPO:0141796', 'abnormal demethylation', 0.55, 4.758907843651163, 1.6178378515809735, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(291047, 'HP:0033013', 'Abnormal salivary cortisol level', 'XPO:0131703', 'abnormal cell division', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(291048, 'HP:0033013', 'Abnormal salivary cortisol level', 'XPO:0141863', 'abnormal lactate metabolic process', 0.4074074074074074, 4.758907843651163, 1.392413123563799, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(291049, 'HP:0033013', 'Abnormal salivary cortisol level', 'XPO:0141908', 'abnormal pyridine metabolic process', 0.44, 4.758907843651163, 1.447038165082909, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(291050, 'HP:0033013', 'Abnormal salivary cortisol level', 'XPO:0100081', 'abnormal anatomical entity in vitro', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(291051, 'HP:0033013', 'Abnormal salivary cortisol level', 'XPO:0107278', 'abnormal medial region', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(291052, 'HP:0033013', 'Abnormal salivary cortisol level', 'XPO:0100009', 'abnormal multi-tissue structure', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(291053, 'HP:0033013', 'Abnormal salivary cortisol level', 'XPO:0101366', 'abnormal morula cell', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(291054, 'HP:0033013', 'Abnormal salivary cortisol level', 'XPO:0100862', 'abnormal blastomere V1', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(291055, 'HP:0033013', 'Abnormal salivary cortisol level', 'XPO:0100721', 'abnormal centromere', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(291056, 'HP:0033013', 'Abnormal salivary cortisol level', 'XPO:0100258', 'abnormal organ part', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(291057, 'HP:0033013', 'Abnormal salivary cortisol level', 'XPO:0100232', 'abnormal lymphatic system', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(291058, 'HP:0033013', 'Abnormal salivary cortisol level', 'XPO:0107253', 'abnormal enteric nervous system', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
