(109420, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0126537', 'abnormally localised hematological system', 0.41935483870967744, 5.574066539846944, 1.5288923359002506, 'HP:0001871', 'Abnormality of blood and blood-forming tissues'),
(109421, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0141791', 'abnormal primary metabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(109422, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0141266', 'abnormal surface breathing', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(109423, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0124923', 'absent hematological system', 0.40625, 5.574066539846944, 1.5048137864243607, 'HP:0001871', 'Abnormality of blood and blood-forming tissues'),
(109424, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0101074', 'abnormal germinal vesicle', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(109425, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0100551', 'abnormal oocyte cortex', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(109426, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0101283', 'abnormal left-ventral blastomere', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(109427, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0100724', 'abnormal kinetochore', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(109428, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0141777', 'abnormal catabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(109429, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0100273', 'abnormal visual system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(109430, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0100610', 'abnormal appendage', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(109431, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0101056', 'abnormal anterior ventral blood island', 0.4642857142857143, 5.574066539846944, 1.6087136056268494, 'HP:0001871', 'Abnormality of blood and blood-forming tissues'),
(109432, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0100754', 'abnormal electrically active cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(109433, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0101378', 'abnormal blastomere D1', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(109434, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0100392', 'abnormal cilium', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(109435, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0100282', 'abnormal pelvic girdle primordium', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(109436, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0100295', 'abnormal extracellular matrix', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(109437, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0141743', 'abnormal chemical homeostasis within a tissue', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(109438, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0141271', 'increased surface breathing', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(109439, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0100081', 'abnormal anatomical entity in vitro', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(109440, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0101547', 'abnormal lampbrush chromosome', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(109441, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0101519', 'abnormal hypobranchial placode', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(109442, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0107264', 'abnormal anterior side', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(109443, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0101202', 'abnormal thymus', 0.41935483870967744, 5.574066539846944, 1.5288923359002506, 'HP:0001871', 'Abnormality of blood and blood-forming tissues'),
(109444, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0107312', 'abnormal filopodium', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(109445, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0131687', 'abnormal astral microtubule', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(109446, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0100481', 'abnormal anatomical line', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(109447, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0107263', 'abnormal anatomical side', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(109448, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0107266', 'abnormal dorsal side', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(109449, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0100186', 'abnormal uveal tract', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(109450, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0100417', 'abnormal dense regular connective tissue', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(109451, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0100786', 'abnormal presumptive axial mesoderm', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(109452, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0100546', 'abnormal whole organism', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(109453, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0101188', 'abnormal posterior ventral blood island', 0.4642857142857143, 5.574066539846944, 1.6087136056268494, 'UPHENO:0004459', 'abnormal hematopoietic system'),
(109454, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0131675', 'abnormal spindle microtubule', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(109455, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0101200', 'abnormal joint region', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(109456, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0100642', 'abnormal gustatory system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(109457, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0141770', 'abnormal urate homeostasis', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(109458, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0100274', 'abnormal sensory system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(109459, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0100969', 'abnormal disaggregated/reaggregated ectoderm treated with activin', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(109460, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0107276', 'abnormal dorsal region', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(109461, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0100002', 'abnormal head', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(109462, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0101072', 'abnormal mitochondrial cloud', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(109463, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0100728', 'abnormal cell condensation', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(109464, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0100004', 'abnormal cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(109465, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0107325', 'abnormal adult thrombocyte', 0.41935483870967744, 5.574066539846944, 1.5288923359002506, 'HP:0001871', 'Abnormality of blood and blood-forming tissues'),
(109466, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0100917', 'abnormal stage III oocyte', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(109467, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0100003', 'abnormal organism subdivision', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(109468, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0141264', 'abnormal schooling behavior', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(109469, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0101157', 'abnormal female organism', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(109470, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0131685', 'abnormal cortical actin cytoskeleton', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(109471, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0101463', 'abnormal right-ventral blastomere', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(109472, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0100258', 'abnormal organ part', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(109473, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0101240', 'abnormal ciliated non-epidermal cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(109474, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0100423', 'abnormal process', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(109475, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0100277', 'abnormal blastocoel', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(109476, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0107269', 'abnormal right side', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(109477, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0100888', 'abnormal microtubule', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(109478, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0131691', 'abnormal molecular function', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(109479, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0101587', 'abnormal hemangioblast', 0.5, 5.574066539846944, 1.6694410052240456, 'HP:0001871', 'Abnormality of blood and blood-forming tissues'),
(109480, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0100006', 'abnormal anatomical structure', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(109481, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0101373', 'abnormal oxygen accumulating cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(109482, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0100363', 'abnormal cardiovascular system', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(109483, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0100912', 'abnormal trabecula', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(109484, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0131667', 'abnormal actin cytoskeleton', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(109485, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0101132', 'abnormal apoptotic cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(109486, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0101061', 'abnormal plasma membrane', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(109487, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0101406', 'abnormal cleavage furrow', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(109488, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0107253', 'abnormal enteric nervous system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(109489, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0100501', 'abnormal urogenital system', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(109490, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0100587', 'abnormal vestibuloauditory system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(109491, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0107324', 'abnormal embryonic thrombocyte', 0.41935483870967744, 5.574066539846944, 1.5288923359002506, 'UPHENO:0004459', 'abnormal hematopoietic system'),
(109492, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0141267', 'abnormal resting posture', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(109493, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0101448', 'abnormal myelin accumulating cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(109494, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0100688', 'abnormal adipose tissue', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(109495, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0100762', 'abnormal intersomitic region', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(109496, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0101096', 'abnormal tendon', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(109497, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0101241', 'abnormal nucleate erythrocyte', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(109498, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0100549', 'abnormal mitotic cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(109499, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0101450', 'abnormal myeloid cell', 0.5, 5.574066539846944, 1.6694410052240456, 'UPHENO:0004459', 'abnormal hematopoietic system'),
(109500, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0100531', 'abnormal proliferative region', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(109501, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0100308', 'abnormal early embryonic cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(109502, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0101405', 'abnormal ring structure', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(109503, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0101113', 'abnormal stage IV oocyte', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(109504, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0100120', 'abnormal genital system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(109505, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0100823', 'abnormal blood', 0.5416666666666666, 5.574066539846944, 1.737609289344729, 'UPHENO:0004459', 'abnormal hematopoietic system'),
(109506, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0107262', 'abnormal left-right axis', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(109507, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0115758', 'abnormally decreased mobility of melanoblast', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(109508, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0100339', 'abnormal circumblastoporal collar', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(109509, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0141714', 'abnormal anterior notochord', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(109510, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0101311', 'abnormal bottle cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(109511, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0101503', 'abnormal organ cortex', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(109512, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0101484', 'abnormal bone marrow', 0.43333333333333335, 5.574066539846944, 1.5541649957239663, 'UPHENO:0004459', 'abnormal hematopoietic system'),
(109513, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0126758', 'abnormally localised blood', 0.41935483870967744, 5.574066539846944, 1.5288923359002506, 'HP:0001871', 'Abnormality of blood and blood-forming tissues'),
(109514, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0100192', 'abnormal epithelium', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(109515, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0101174', 'abnormal articular system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(109516, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0100533', 'abnormal melanoblast', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(109517, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0100842', 'abnormal left-dorsal blastomere', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(109518, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0107273', 'abnormal basal region', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(109519, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0131666', 'abnormal adherens junction', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(109520, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0101575', 'abnormal vitelline membrane', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(109521, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0100285', 'abnormal progenitor cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(109522, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0100427', 'abnormal olfactory system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(109523, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0101221', 'abnormal larval immune system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(109524, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0141771', 'abnormal urea homeostasis', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(109525, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0141778', 'abnormal biosynthetic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(109526, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0100503', 'abnormal blastomere D2', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(109527, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0100915', 'abnormal dermal system', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(109528, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0100665', 'abnormal egg jelly', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(109529, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0100151', 'abnormal primordium', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(109530, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0100574', 'abnormal gastrula cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(109531, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0100856', 'abnormal simple organ', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(109532, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0100225', 'abnormal endocrine system', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(109533, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0100791', 'abnormal multiciliated cell precursor', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(109534, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0100031', 'abnormal central nervous system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(109535, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0100573', 'abnormal extraembryonic structure', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(109536, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0141783', 'abnormal collagen metabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(109537, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0101326', 'abnormal cementoblast', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(109538, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0100913', 'abnormal Brachets cleft', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(109539, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0131723', 'abnormal pathway-restricted SMAD protein phosphorylation', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(109540, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0101535', 'abnormal absorptive cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(109541, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0115505', 'dead whole organism', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(109542, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0100465', 'abnormal skeletal system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(109543, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0101107', 'abnormal erythroid cell', 0.5, 5.574066539846944, 1.6694410052240456, 'HP:0001871', 'Abnormality of blood and blood-forming tissues'),
(109544, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0107265', 'abnormal posterior side', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(109545, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0100032', 'abnormal nervous system', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(109546, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0100581', 'abnormal immune system', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(109547, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0141786', 'abnormal pigment metabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(109548, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0101409', 'abnormal perivitelline space', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(109549, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0100231', 'abnormal compound organ', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(109550, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0100894', 'abnormal nucleus', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(109551, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0100638', 'abnormal polar body', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(109552, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0100251', 'abnormal proteinaceous extracellular matrix', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(109553, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0101467', 'abnormal alkali secreting cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(109554, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0107323', 'abnormal thrombocyte', 0.43333333333333335, 5.574066539846944, 1.5541649957239663, 'UPHENO:0004459', 'abnormal hematopoietic system'),
(109555, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0100999', 'abnormal serous membrane', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(109556, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0100674', 'abnormal secondary oogonium', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(109557, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0116494', 'absent biological process', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(109558, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0107268', 'abnormal left side', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(109559, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0131677', 'abnormal actin filament', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(109560, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0101228', 'abnormal mesenchymal stem cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(109561, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0100014', 'abnormal tissue', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(109562, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0100673', 'abnormal anterior dorsal lateral plate region', 0.41935483870967744, 5.574066539846944, 1.5288923359002506, 'UPHENO:0004459', 'abnormal hematopoietic system'),
(109563, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0101498', 'abnormal stage II oocyte', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(109564, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0102004', 'abnormal hematological system morphology', 0.41935483870967744, 5.574066539846944, 1.5288923359002506, 'HP:0001871', 'Abnormality of blood and blood-forming tissues'),
(109565, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0101411', 'abnormal marginal zone (sensu neural)', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(109566, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0141784', 'abnormal cellular hormone metabolic process', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(109567, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0142051', 'abnormal cerebrospinal fluid', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(109568, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0100902', 'abnormal spermatocyte', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(109569, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0107284', 'abnormal migrating myoblast', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(109570, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0102455', 'abnormal blood morphology', 0.41935483870967744, 5.574066539846944, 1.5288923359002506, 'UPHENO:0004459', 'abnormal hematopoietic system'),
(109571, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0116434', 'abnormal biological process', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(109572, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0100202', 'abnormal embryo', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(109573, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0100742', 'abnormal musculoskeletal system', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(109574, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0115391', 'abnormally undifferentiated alimentary system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(109575, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0125135', 'absent blood', 0.40625, 5.574066539846944, 1.5048137864243607, 'HP:0001871', 'Abnormality of blood and blood-forming tissues'),
(109576, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0101220', 'abnormal centriole', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(109577, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0141792', 'abnormal small molecule metabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(109578, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0100989', 'abnormal right blastomere', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(109579, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0100104', 'abnormal embryonic structure', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(109580, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0107285', 'abnormal flexural organ', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(109581, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0100415', 'abnormal secretory epithelial cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(109582, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0131725', 'abnormal phosphorylation of RNA polymerase II C-terminal domain', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(109583, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0100416', 'abnormal ligament', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(109584, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0101497', 'abnormal ciliary axoneme', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(109585, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0101078', 'abnormal mucous gland', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(109586, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0100135', 'abnormal surface structure', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(109587, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0100239', 'abnormal acellular anatomical structure', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(109588, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0141499', 'abnormal tadpole', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(109589, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0100232', 'abnormal lymphatic system', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(109590, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0101389', 'abnormal wedge region', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(109591, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0141781', 'abnormal secondary metabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(109592, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0141748', 'abnormal gas homeostasis', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(109593, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0101212', 'abnormal glomeral mesenchyme', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(109594, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0101569', 'abnormal activin-induced ectoderm', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(109595, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0100547', 'abnormal blastomere V2', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(109596, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0141775', 'abnormal nitrogen compound metabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(109597, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0101451', 'abnormal dorsal lymph space', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(109598, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0100070', 'abnormal anatomical system', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(109599, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0100152', 'abnormal alimentary system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(109600, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0141738', 'abnormal carbon dioxide homeostasis', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(109601, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0141272', 'absent surface breathing', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(109602, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0100026', 'abnormal germ cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(109603, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0100802', 'abnormal exocrine cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(109604, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0101136', 'abnormal ooplasm', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(109605, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0100511', 'abnormal stylopod', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(109606, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0100028', 'abnormal anatomical cluster', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(109607, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0141797', 'abnormal hydrogen metabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(109608, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0100025', 'abnormal oocyte', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(109609, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0100377', 'abnormal connective tissue', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(109610, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0141794', 'abnormal prosthetic group metabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(109611, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0100887', 'abnormal right-dorsal blastomere', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(109612, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0107271', 'abnormal apical region', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(109613, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0100557', 'abnormal prime meridian', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(109614, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0141718', 'abnormal posterior notochord', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(109615, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0107259', 'abnormal animal-vegetal axis', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(109616, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0101461', 'abnormal sperm entry point', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(109617, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0141841', 'abnormality of whole organism mass', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(109618, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0101109', 'abnormal egg cell-free extract', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(109619, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0107261', 'abnormal dorsal-ventral axis', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(109620, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0100023', 'abnormal mesenchyme', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(109621, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0100010', 'abnormal multicellular anatomical structure', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(109622, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0100640', 'abnormal notochordal sheath', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(109623, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0115509', 'abnormally semi-viable whole organism', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(109624, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0107278', 'abnormal medial region', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(109625, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0100372', 'abnormal hematological system', 0.5909090909090909, 5.574066539846944, 1.8148737123358583, 'HP:0001871', 'Abnormality of blood and blood-forming tissues'),
(109626, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0101071', 'abnormal endoplasmic reticulum', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(109627, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0107339', 'abnormal yolk platelet', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(109628, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0100069', 'abnormal urinary system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(109629, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0100205', 'abnormal limb segment', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(109630, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0100991', 'abnormal iliac process primordium', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(109631, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0141772', 'abnormal water homeostasis', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(109632, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0100721', 'abnormal centromere', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(109633, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0100784', 'abnormal left blastomere', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(109634, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0101141', 'abnormal Keller explant', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(109635, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0107272', 'abnormal axial region', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(109636, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0100164', 'abnormal neural nucleus', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(109637, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0100585', 'abnormal elastica externa', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(109638, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0107258', 'abnormal anatomical axis', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(109639, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0100477', 'abnormal pericyte', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(109640, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0100653', 'abnormal myoblast', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(109641, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0100626', 'abnormal primordial germ cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(109642, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0100807', 'abnormal matrix-based tissue', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(109643, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0100715', 'abnormal ciliated cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(109644, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0101168', 'abnormal circulating cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(109645, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0100394', 'abnormal marginal zone', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(109646, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0101468', 'abnormal stage I oocyte', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(109647, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0100745', 'abnormal anterior lymph sac', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(109648, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0100337', 'abnormal zygote', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(109649, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0141776', 'abnormal metabolic process', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(109650, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0141715', 'abnormal septum', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(109651, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0100265', 'abnormal sensory epithelial cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(109652, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0100402', 'abnormal zeugopod', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(109653, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0142056', 'abnormal main body axis', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(109654, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0100162', 'abnormal presumptive rhombomere', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(109655, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0101362', 'abnormal vegetal cortex', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(109656, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0100616', 'abnormal ventral blood island', 0.48148148148148145, 5.574066539846944, 1.6382337487311942, 'HP:0001871', 'Abnormality of blood and blood-forming tissues'),
(109657, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0100344', 'abnormal portion of organism substance', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(109658, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0100862', 'abnormal blastomere V1', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(109659, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0100293', 'abnormal duct', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(109660, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0101472', 'abnormal zygote cortex', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(109661, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0100899', 'abnormal secondary spermatogonium', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(109662, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0101435', 'abnormal paracrine cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(109663, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0100009', 'abnormal multi-tissue structure', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(109664, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0100084', 'abnormal anatomical group', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(109665, 'HP:0002625', 'Deep venous thrombosis', 'XPO:0100515', 'abnormal somatic stem cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(109666, 'HP:0000198', 'Absence of Stensen duct', 'XPO:0101567', 'abnormal tongue', 0.5614035087719298, 7.884497199543557, 2.103897429231332, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(109667, 'HP:0000198', 'Absence of Stensen duct', 'XPO:0115393', 'abnormally decreased volume of oral cavity', 0.4383561643835616, 7.884497199543557, 1.859090624602482, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(109668, 'HP:0000198', 'Absence of Stensen duct', 'XPO:0127750', 'abnormally localised tongue', 0.47058823529411764, 7.884497199543557, 1.9262273031277009, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(109669, 'HP:0000198', 'Absence of Stensen duct', 'XPO:0130628', 'increased size of the oral cavity', 0.4507042253521127, 7.884497199543557, 1.885093154889482, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(109670, 'HP:0000198', 'Absence of Stensen duct', 'XPO:0103138', 'abnormal upper jaw morphology', 0.4125, 8.81758714901448, 1.9071588027661652, 'UPHENO:0087585', 'abnormal midface morphology'),
(109671, 'HP:0000198', 'Absence of Stensen duct', 'XPO:0140789', 'abnormally necrotic roof of mouth', 0.40540540540540543, 7.312692920701687, 1.7218029033900208, 'UPHENO:0076800', 'abnormal mouth morphology'),
(109672, 'HP:0000198', 'Absence of Stensen duct', 'XPO:0103735', 'increased size of the mouth', 0.4266666666666667, 7.884497199543557, 1.8341352563188784, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(109673, 'HP:0000198', 'Absence of Stensen duct', 'XPO:0115558', 'abnormally incomplete structure of mouth', 0.44776119402985076, 7.312692920701687, 1.8095137782694621, 'UPHENO:0076800', 'abnormal mouth morphology'),
(109674, 'HP:0000198', 'Absence of Stensen duct', 'XPO:0102279', 'abnormal mouth morphology', 0.45454545454545453, 7.312692920701687, 1.8231706797751206, 'UPHENO:0076800', 'abnormal mouth morphology'),
(109675, 'HP:0000198', 'Absence of Stensen duct', 'XPO:0129152', 'decreased size of the oral cavity', 0.4507042253521127, 7.884497199543557, 1.885093154889482, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(109676, 'HP:0000198', 'Absence of Stensen duct', 'XPO:0128105', 'decreased size of the tongue', 0.4050632911392405, 7.884497199543557, 1.78709831420245, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(109677, 'HP:0000198', 'Absence of Stensen duct', 'XPO:0140626', 'abnormally necrotic tongue', 0.4507042253521127, 7.884497199543557, 1.885093154889482, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(109678, 'HP:0000198', 'Absence of Stensen duct', 'XPO:0103352', 'decreased size of the mouth', 0.4266666666666667, 7.884497199543557, 1.8341352563188784, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(109679, 'HP:0000198', 'Absence of Stensen duct', 'XPO:0126089', 'absent tongue', 0.45714285714285713, 7.884497199543557, 1.8985103573418285, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(109680, 'HP:0000198', 'Absence of Stensen duct', 'XPO:0141311', 'abnormal roof of mouth morphology', 0.43478260869565216, 7.312692920701687, 1.7830961007901136, 'UPHENO:0076800', 'abnormal mouth morphology'),
(109681, 'HP:0000198', 'Absence of Stensen duct', 'XPO:0103199', 'abnormal tongue morphology', 0.48484848484848486, 7.884497199543557, 1.9551947527013303, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(109682, 'HP:0000198', 'Absence of Stensen duct', 'XPO:0103096', 'abnormal oral cavity morphology', 0.48484848484848486, 7.884497199543557, 1.9551947527013303, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(109683, 'HP:0033305', 'Abnormal circulating fetuin A concentration', 'XPO:0141869', 'abnormal alpha-amino acid metabolic process', 0.40350877192982454, 7.41682187759612, 1.729957423594889, 'HP:0430071', 'Abnormal circulating organic compound concentration'),
(109684, 'HP:0033305', 'Abnormal circulating fetuin A concentration', 'XPO:0141873', 'abnormal tricarboxylic acid metabolic process', 0.4339622641509434, 7.41682187759612, 1.7940515084037758, 'HP:0430071', 'Abnormal circulating organic compound concentration'),
(109685, 'HP:0034445', 'Reduced gamma-glutamyltransferase level', 'XPO:0141777', 'abnormal catabolic process', 0.5, 4.758907843651163, 1.5425478669479211, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(109686, 'HP:0034445', 'Reduced gamma-glutamyltransferase level', 'XPO:0100721', 'abnormal centromere', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(109687, 'HP:0034445', 'Reduced gamma-glutamyltransferase level', 'XPO:0141910', 'abnormal D-ribose metabolic process', 0.4074074074074074, 4.758907843651163, 1.392413123563799, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(109688, 'HP:0034445', 'Reduced gamma-glutamyltransferase level', 'XPO:0141776', 'abnormal metabolic process', 0.55, 4.758907843651163, 1.6178378515809735, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(109689, 'HP:0034445', 'Reduced gamma-glutamyltransferase level', 'XPO:0131666', 'abnormal adherens junction', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(109690, 'HP:0034445', 'Reduced gamma-glutamyltransferase level', 'XPO:0141748', 'abnormal gas homeostasis', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(109691, 'HP:0034445', 'Reduced gamma-glutamyltransferase level', 'XPO:0101237', 'abnormal mucus secreting cell', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(109692, 'HP:0034445', 'Reduced gamma-glutamyltransferase level', 'XPO:0141877', 'abnormal 2-deoxyribose 1-phosphate metabolic process', 0.44, 4.758907843651163, 1.447038165082909, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(109693, 'HP:0034445', 'Reduced gamma-glutamyltransferase level', 'XPO:0131723', 'abnormal pathway-restricted SMAD protein phosphorylation', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(109694, 'HP:0034445', 'Reduced gamma-glutamyltransferase level', 'XPO:0100004', 'abnormal cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(109695, 'HP:0034445', 'Reduced gamma-glutamyltransferase level', 'XPO:0100289', 'abnormal chondroblast', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(109696, 'HP:0034445', 'Reduced gamma-glutamyltransferase level', 'XPO:0141743', 'abnormal chemical homeostasis within a tissue', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(109697, 'HP:0034445', 'Reduced gamma-glutamyltransferase level', 'XPO:0100501', 'abnormal urogenital system', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(109698, 'HP:0034445', 'Reduced gamma-glutamyltransferase level', 'XPO:0141784', 'abnormal cellular hormone metabolic process', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(109699, 'HP:0034445', 'Reduced gamma-glutamyltransferase level', 'XPO:0100032', 'abnormal nervous system', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(109700, 'HP:0034445', 'Reduced gamma-glutamyltransferase level', 'XPO:0116494', 'absent biological process', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(109701, 'HP:0034445', 'Reduced gamma-glutamyltransferase level', 'XPO:0100626', 'abnormal primordial germ cell', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(109702, 'HP:0034445', 'Reduced gamma-glutamyltransferase level', 'XPO:0141786', 'abnormal pigment metabolic process', 0.5, 4.758907843651163, 1.5425478669479211, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(109703, 'HP:0034445', 'Reduced gamma-glutamyltransferase level', 'XPO:0141271', 'increased surface breathing', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(109704, 'HP:0034445', 'Reduced gamma-glutamyltransferase level', 'XPO:0141798', 'abnormal lipid metabolic process', 0.4583333333333333, 4.758907843651163, 1.4768771428276568, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(109705, 'HP:0034445', 'Reduced gamma-glutamyltransferase level', 'XPO:0101141', 'abnormal Keller explant', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(109706, 'HP:0034445', 'Reduced gamma-glutamyltransferase level', 'XPO:0100533', 'abnormal melanoblast', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(109707, 'HP:0034445', 'Reduced gamma-glutamyltransferase level', 'XPO:0100956', 'abnormal centrosome', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(109708, 'HP:0034445', 'Reduced gamma-glutamyltransferase level', 'XPO:0100791', 'abnormal multiciliated cell precursor', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(109709, 'HP:0034445', 'Reduced gamma-glutamyltransferase level', 'XPO:0100429', 'abnormal spermatid', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(109710, 'HP:0034445', 'Reduced gamma-glutamyltransferase level', 'XPO:0141266', 'abnormal surface breathing', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(109711, 'HP:0034445', 'Reduced gamma-glutamyltransferase level', 'XPO:0141783', 'abnormal collagen metabolic process', 0.5, 4.758907843651163, 1.5425478669479211, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(109712, 'HP:0034445', 'Reduced gamma-glutamyltransferase level', 'XPO:0141908', 'abnormal pyridine metabolic process', 0.4074074074074074, 4.758907843651163, 1.392413123563799, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(109713, 'HP:0034445', 'Reduced gamma-glutamyltransferase level', 'XPO:0141795', 'abnormal glycosylation', 0.4583333333333333, 4.758907843651163, 1.4768771428276568, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(109714, 'HP:0034445', 'Reduced gamma-glutamyltransferase level', 'XPO:0101547', 'abnormal lampbrush chromosome', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(109715, 'HP:0034445', 'Reduced gamma-glutamyltransferase level', 'XPO:0141892', 'abnormal inositol metabolic process', 0.4583333333333333, 4.758907843651163, 1.4768771428276568, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(109716, 'HP:0034445', 'Reduced gamma-glutamyltransferase level', 'XPO:0100006', 'abnormal anatomical structure', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(109717, 'HP:0034445', 'Reduced gamma-glutamyltransferase level', 'XPO:0101132', 'abnormal apoptotic cell', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(109718, 'HP:0034445', 'Reduced gamma-glutamyltransferase level', 'XPO:00000000', 'Xenopus phenotype', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(109719, 'HP:0034445', 'Reduced gamma-glutamyltransferase level', 'XPO:0141794', 'abnormal prosthetic group metabolic process', 0.5, 4.758907843651163, 1.5425478669479211, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(109720, 'HP:0034445', 'Reduced gamma-glutamyltransferase level', 'XPO:0100907', 'abnormal cytoplasm', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(109721, 'HP:0034445', 'Reduced gamma-glutamyltransferase level', 'XPO:0100852', 'abnormal interdigital region', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(109722, 'HP:0034445', 'Reduced gamma-glutamyltransferase level', 'XPO:0100581', 'abnormal immune system', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(109723, 'HP:0034445', 'Reduced gamma-glutamyltransferase level', 'XPO:0100691', 'abnormal keratin accumulating cell', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(109724, 'HP:0034445', 'Reduced gamma-glutamyltransferase level', 'XPO:0100437', 'abnormal proepicardium', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(109725, 'HP:0034445', 'Reduced gamma-glutamyltransferase level', 'XPO:0141781', 'abnormal secondary metabolic process', 0.5, 4.758907843651163, 1.5425478669479211, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(109726, 'HP:0034445', 'Reduced gamma-glutamyltransferase level', 'XPO:0141272', 'absent surface breathing', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(109727, 'HP:0034445', 'Reduced gamma-glutamyltransferase level', 'XPO:0100969', 'abnormal disaggregated/reaggregated ectoderm treated with activin', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(109728, 'HP:0034445', 'Reduced gamma-glutamyltransferase level', 'XPO:0100754', 'abnormal electrically active cell', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(109729, 'HP:0034445', 'Reduced gamma-glutamyltransferase level', 'XPO:0101569', 'abnormal activin-induced ectoderm', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(109730, 'HP:0034445', 'Reduced gamma-glutamyltransferase level', 'XPO:0141264', 'abnormal schooling behavior', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(109731, 'HP:0034445', 'Reduced gamma-glutamyltransferase level', 'XPO:0141791', 'abnormal primary metabolic process', 0.5, 4.758907843651163, 1.5425478669479211, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(109732, 'HP:0034445', 'Reduced gamma-glutamyltransferase level', 'XPO:0101297', 'abnormal barrier cell', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(109733, 'HP:0034445', 'Reduced gamma-glutamyltransferase level', 'XPO:0141898', 'abnormal maltose metabolic process', 0.44, 4.758907843651163, 1.447038165082909, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(109734, 'HP:0034445', 'Reduced gamma-glutamyltransferase level', 'XPO:0101535', 'abnormal absorptive cell', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(109735, 'HP:0034445', 'Reduced gamma-glutamyltransferase level', 'XPO:0141267', 'abnormal resting posture', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(109736, 'HP:0034445', 'Reduced gamma-glutamyltransferase level', 'XPO:0141859', 'abnormal lactose catabolic process', 0.4074074074074074, 4.758907843651163, 1.392413123563799, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(109737, 'HP:0034445', 'Reduced gamma-glutamyltransferase level', 'XPO:0107312', 'abnormal filopodium', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(109738, 'HP:0034445', 'Reduced gamma-glutamyltransferase level', 'XPO:0100515', 'abnormal somatic stem cell', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(109739, 'HP:0034445', 'Reduced gamma-glutamyltransferase level', 'XPO:0131725', 'abnormal phosphorylation of RNA polymerase II C-terminal domain', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(109740, 'HP:0034445', 'Reduced gamma-glutamyltransferase level', 'XPO:0100549', 'abnormal mitotic cell', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(109741, 'HP:0034445', 'Reduced gamma-glutamyltransferase level', 'XPO:0101241', 'abnormal nucleate erythrocyte', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(109742, 'HP:0034445', 'Reduced gamma-glutamyltransferase level', 'XPO:0141778', 'abnormal biosynthetic process', 0.5, 4.758907843651163, 1.5425478669479211, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(109743, 'HP:0034445', 'Reduced gamma-glutamyltransferase level', 'XPO:0141904', 'abnormal glucosamine metabolic process', 0.5, 4.758907843651163, 1.5425478669479211, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(109744, 'HP:0034445', 'Reduced gamma-glutamyltransferase level', 'XPO:0141797', 'abnormal hydrogen metabolic process', 0.5, 4.758907843651163, 1.5425478669479211, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(109745, 'HP:0034445', 'Reduced gamma-glutamyltransferase level', 'XPO:0100232', 'abnormal lymphatic system', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(109746, 'HP:0034445', 'Reduced gamma-glutamyltransferase level', 'XPO:0101228', 'abnormal mesenchymal stem cell', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(109747, 'HP:0034445', 'Reduced gamma-glutamyltransferase level', 'XPO:0141796', 'abnormal demethylation', 0.5, 4.758907843651163, 1.5425478669479211, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(109748, 'HP:0034445', 'Reduced gamma-glutamyltransferase level', 'XPO:0101448', 'abnormal myelin accumulating cell', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(109749, 'HP:0034445', 'Reduced gamma-glutamyltransferase level', 'XPO:0100026', 'abnormal germ cell', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(109750, 'HP:0034445', 'Reduced gamma-glutamyltransferase level', 'XPO:0100344', 'abnormal portion of organism substance', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(109751, 'HP:0034445', 'Reduced gamma-glutamyltransferase level', 'XPO:0141911', 'abnormal ribose phosphate metabolic process', 0.44, 4.758907843651163, 1.447038165082909, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(109752, 'HP:0034445', 'Reduced gamma-glutamyltransferase level', 'XPO:0107284', 'abnormal migrating myoblast', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(109753, 'HP:0034445', 'Reduced gamma-glutamyltransferase level', 'XPO:0100674', 'abnormal secondary oogonium', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(109754, 'HP:0034445', 'Reduced gamma-glutamyltransferase level', 'XPO:0100638', 'abnormal polar body', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(109755, 'HP:0034445', 'Reduced gamma-glutamyltransferase level', 'XPO:0141263', 'abnormal visually guided collision avoidance behavior', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(109756, 'HP:0034445', 'Reduced gamma-glutamyltransferase level', 'XPO:0141265', 'abnormal escape behavior', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(109757, 'HP:0034445', 'Reduced gamma-glutamyltransferase level', 'XPO:0141276', 'decreased surface breathing', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(109758, 'HP:0034445', 'Reduced gamma-glutamyltransferase level', 'XPO:0141900', 'abnormal mannose metabolic process', 0.4074074074074074, 4.758907843651163, 1.392413123563799, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(109759, 'HP:0034445', 'Reduced gamma-glutamyltransferase level', 'XPO:0141790', 'abnormal cellular metabolic process', 0.4782608695652174, 4.758907843651163, 1.508641575552437, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(109760, 'HP:0034445', 'Reduced gamma-glutamyltransferase level', 'XPO:0141775', 'abnormal nitrogen compound metabolic process', 0.5, 4.758907843651163, 1.5425478669479211, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(109761, 'HP:0034445', 'Reduced gamma-glutamyltransferase level', 'XPO:0107258', 'abnormal anatomical axis', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(109762, 'HP:0034445', 'Reduced gamma-glutamyltransferase level', 'XPO:0141860', 'abnormal malate-aspartate shuttle', 0.4782608695652174, 4.758907843651163, 1.508641575552437, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(109763, 'HP:0034445', 'Reduced gamma-glutamyltransferase level', 'XPO:0100715', 'abnormal ciliated cell', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(109764, 'HP:0034445', 'Reduced gamma-glutamyltransferase level', 'XPO:0100081', 'abnormal anatomical entity in vitro', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(109765, 'HP:0034445', 'Reduced gamma-glutamyltransferase level', 'XPO:0141782', 'abnormal methylation', 0.5, 4.758907843651163, 1.5425478669479211, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(109766, 'HP:0034445', 'Reduced gamma-glutamyltransferase level', 'XPO:0131667', 'abnormal actin cytoskeleton', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(109767, 'HP:0034445', 'Reduced gamma-glutamyltransferase level', 'XPO:0100481', 'abnormal anatomical line', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(109768, 'HP:0034445', 'Reduced gamma-glutamyltransferase level', 'XPO:0141789', 'abnormal hormone catabolic process', 0.4230769230769231, 4.758907843651163, 1.418937661667548, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(109769, 'HP:0034445', 'Reduced gamma-glutamyltransferase level', 'XPO:0100902', 'abnormal spermatocyte', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(109770, 'HP:0034445', 'Reduced gamma-glutamyltransferase level', 'XPO:0101004', 'abnormal acid secreting cell', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(109771, 'HP:0034445', 'Reduced gamma-glutamyltransferase level', 'XPO:0141772', 'abnormal water homeostasis', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(109772, 'HP:0034445', 'Reduced gamma-glutamyltransferase level', 'XPO:0100477', 'abnormal pericyte', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(109773, 'HP:0034445', 'Reduced gamma-glutamyltransferase level', 'XPO:0141883', 'abnormal glycerol metabolic process', 0.4074074074074074, 4.758907843651163, 1.392413123563799, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(109774, 'HP:0034445', 'Reduced gamma-glutamyltransferase level', 'XPO:0142057', 'abnormal desmosome', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(109775, 'HP:0034445', 'Reduced gamma-glutamyltransferase level', 'XPO:0101373', 'abnormal oxygen accumulating cell', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(109776, 'HP:0034445', 'Reduced gamma-glutamyltransferase level', 'XPO:0141852', 'abnormal glucose metabolic process', 0.4074074074074074, 4.758907843651163, 1.392413123563799, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(109777, 'HP:0034445', 'Reduced gamma-glutamyltransferase level', 'XPO:0116434', 'abnormal biological process', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(109778, 'HP:0034445', 'Reduced gamma-glutamyltransferase level', 'XPO:0141881', 'abnormal fructose metabolic process', 0.4074074074074074, 4.758907843651163, 1.392413123563799, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(109779, 'HP:0034445', 'Reduced gamma-glutamyltransferase level', 'XPO:0100308', 'abnormal early embryonic cell', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(109780, 'HP:0034445', 'Reduced gamma-glutamyltransferase level', 'XPO:0101326', 'abnormal cementoblast', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(109781, 'HP:0034445', 'Reduced gamma-glutamyltransferase level', 'XPO:0100108', 'abnormal cell part', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(109782, 'HP:0034445', 'Reduced gamma-glutamyltransferase level', 'XPO:0101110', 'abnormal cell-free extract', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(109783, 'HP:0034445', 'Reduced gamma-glutamyltransferase level', 'XPO:0100976', 'abnormal multiciliated cell', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(109784, 'HP:0034445', 'Reduced gamma-glutamyltransferase level', 'XPO:0141771', 'abnormal urea homeostasis', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(109785, 'HP:0034445', 'Reduced gamma-glutamyltransferase level', 'XPO:0101467', 'abnormal alkali secreting cell', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(109786, 'HP:0034445', 'Reduced gamma-glutamyltransferase level', 'XPO:0100704', 'abnormal Merkel cell', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(109787, 'HP:0034445', 'Reduced gamma-glutamyltransferase level', 'XPO:0131691', 'abnormal molecular function', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(109788, 'HP:0034445', 'Reduced gamma-glutamyltransferase level', 'XPO:0101071', 'abnormal endoplasmic reticulum', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(109789, 'HP:0034445', 'Reduced gamma-glutamyltransferase level', 'XPO:0141788', 'abnormal hormone biosynthetic process', 0.4230769230769231, 4.758907843651163, 1.418937661667548, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(109790, 'HP:0034445', 'Reduced gamma-glutamyltransferase level', 'XPO:0141767', 'abnormal temperature homeostasis', 0.4230769230769231, 4.758907843651163, 1.418937661667548, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(109791, 'HP:0034445', 'Reduced gamma-glutamyltransferase level', 'XPO:0141907', 'abnormal putrescine metabolic process', 0.4583333333333333, 4.758907843651163, 1.4768771428276568, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(109792, 'HP:0034445', 'Reduced gamma-glutamyltransferase level', 'XPO:0141792', 'abnormal small molecule metabolic process', 0.5, 4.758907843651163, 1.5425478669479211, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(109793, 'HP:0034445', 'Reduced gamma-glutamyltransferase level', 'XPO:0101513', 'abnormal basal body', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(109794, 'HP:0034445', 'Reduced gamma-glutamyltransferase level', 'XPO:0100285', 'abnormal progenitor cell', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(109795, 'HP:0034445', 'Reduced gamma-glutamyltransferase level', 'XPO:0101333', 'abnormal barrier epithelial cell', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(109796, 'HP:0034445', 'Reduced gamma-glutamyltransferase level', 'XPO:0141854', 'abnormal glutathione metabolic process', 0.4074074074074074, 4.758907843651163, 1.392413123563799, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(109797, 'HP:0034445', 'Reduced gamma-glutamyltransferase level', 'XPO:0141903', 'abnormal inositol phosphate metabolic process', 0.4074074074074074, 4.758907843651163, 1.392413123563799, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(109798, 'HP:0034445', 'Reduced gamma-glutamyltransferase level', 'XPO:0101264', 'abnormal mitotic spindle', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(109799, 'HP:0034445', 'Reduced gamma-glutamyltransferase level', 'XPO:0100258', 'abnormal organ part', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(109800, 'HP:0034445', 'Reduced gamma-glutamyltransferase level', 'XPO:0100899', 'abnormal secondary spermatogonium', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(109801, 'HP:0034445', 'Reduced gamma-glutamyltransferase level', 'XPO:0101435', 'abnormal paracrine cell', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(109802, 'HP:0034445', 'Reduced gamma-glutamyltransferase level', 'XPO:0101061', 'abnormal plasma membrane', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(109803, 'HP:0034445', 'Reduced gamma-glutamyltransferase level', 'XPO:0141745', 'abnormal creatinine homeostasis', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(109804, 'HP:0034445', 'Reduced gamma-glutamyltransferase level', 'XPO:0100888', 'abnormal microtubule', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(109805, 'HP:0034445', 'Reduced gamma-glutamyltransferase level', 'XPO:0141738', 'abnormal carbon dioxide homeostasis', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(109806, 'HP:0034445', 'Reduced gamma-glutamyltransferase level', 'XPO:0100172', 'abnormal stem cell', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(109807, 'HP:0034445', 'Reduced gamma-glutamyltransferase level', 'XPO:0141850', 'abnormal galactose metabolic process', 0.4074074074074074, 4.758907843651163, 1.392413123563799, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(109808, 'HP:0034445', 'Reduced gamma-glutamyltransferase level', 'XPO:0100802', 'abnormal exocrine cell', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(109809, 'HP:0034445', 'Reduced gamma-glutamyltransferase level', 'XPO:0131694', 'abnormal RNA polymerase II activity', 0.44, 4.758907843651163, 1.447038165082909, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(109810, 'HP:0034445', 'Reduced gamma-glutamyltransferase level', 'XPO:0100724', 'abnormal kinetochore', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(109811, 'HP:0034445', 'Reduced gamma-glutamyltransferase level', 'XPO:0100894', 'abnormal nucleus', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(109812, 'HP:0034445', 'Reduced gamma-glutamyltransferase level', 'XPO:0100317', 'abnormal respiratory system', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(109813, 'HP:0034445', 'Reduced gamma-glutamyltransferase level', 'XPO:0141770', 'abnormal urate homeostasis', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(109814, 'HP:0034445', 'Reduced gamma-glutamyltransferase level', 'XPO:0100225', 'abnormal endocrine system', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(109815, 'HP:0034445', 'Reduced gamma-glutamyltransferase level', 'XPO:0141880', 'abnormal ethanolamine metabolic process', 0.4230769230769231, 4.758907843651163, 1.418937661667548, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(109816, 'HP:0034445', 'Reduced gamma-glutamyltransferase level', 'XPO:0100372', 'abnormal hematological system', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(109817, 'HP:0034445', 'Reduced gamma-glutamyltransferase level', 'XPO:0100653', 'abnormal myoblast', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(109818, 'HP:0034445', 'Reduced gamma-glutamyltransferase level', 'XPO:0141884', 'abnormal phosphagen metabolic process', 0.4074074074074074, 4.758907843651163, 1.392413123563799, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(109819, 'HP:0034445', 'Reduced gamma-glutamyltransferase level', 'XPO:0141787', 'abnormal hormone metabolic process', 0.5, 4.758907843651163, 1.5425478669479211, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(109820, 'HP:0034445', 'Reduced gamma-glutamyltransferase level', 'XPO:0101240', 'abnormal ciliated non-epidermal cell', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(109821, 'HP:0034445', 'Reduced gamma-glutamyltransferase level', 'XPO:0141864', 'abnormal 5-methylcytosine metabolic process', 0.4074074074074074, 4.758907843651163, 1.392413123563799, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(109822, 'HP:0034445', 'Reduced gamma-glutamyltransferase level', 'XPO:0100025', 'abnormal oocyte', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(109823, 'HP:0034445', 'Reduced gamma-glutamyltransferase level', 'XPO:0100337', 'abnormal zygote', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(109824, 'HP:0034445', 'Reduced gamma-glutamyltransferase level', 'XPO:0100546', 'abnormal whole organism', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(109825, 'HP:0040260', 'Decreased size of nasopharyngeal adenoids', 'XPO:0127174', 'abnormally localised aortic arch 1', 0.4166666666666667, 8.127241455820435, 1.8402039578785412, 'HP:0000600', 'Abnormality of the pharynx'),
(109826, 'HP:0040260', 'Decreased size of nasopharyngeal adenoids', 'XPO:0125251', 'absent aortic arch', 0.41237113402061853, 8.127241455820435, 1.8306937962412106, 'HP:0000600', 'Abnormality of the pharynx'),
(109827, 'HP:0040260', 'Decreased size of nasopharyngeal adenoids', 'XPO:0103106', 'abnormal aortic arch 5 morphology', 0.411214953271028, 8.872199840740173, 1.9100736223824444, 'HP:0033151', 'Abnormal pharynx morphology'),
(109828, 'HP:0040260', 'Decreased size of nasopharyngeal adenoids', 'XPO:0101210', 'abnormal aortic arch 2', 0.47619047619047616, 8.127241455820435, 1.9672607806191105, 'HP:0000600', 'Abnormality of the pharynx'),
(109829, 'HP:0040260', 'Decreased size of nasopharyngeal adenoids', 'XPO:0100117', 'abnormal aortic arch', 0.4819277108433735, 8.127241455820435, 1.979076266917197, 'HP:0000600', 'Abnormality of the pharynx'),
(109830, 'HP:0040260', 'Decreased size of nasopharyngeal adenoids', 'XPO:0101894', 'abnormal aortic arch 4 morphology', 0.4036697247706422, 8.872199840740173, 1.8924688815993043, 'HP:0033151', 'Abnormal pharynx morphology'),
(109831, 'HP:0040260', 'Decreased size of nasopharyngeal adenoids', 'XPO:0100262', 'abnormal aortic arch 4', 0.47619047619047616, 8.127241455820435, 1.9672607806191105, 'HP:0000600', 'Abnormality of the pharynx'),
(109832, 'HP:0040260', 'Decreased size of nasopharyngeal adenoids', 'XPO:0101749', 'abnormal aortic arch morphology', 0.41904761904761906, 8.872199840740173, 1.9281789903888162, 'HP:0033151', 'Abnormal pharynx morphology'),
(109833, 'HP:0040260', 'Decreased size of nasopharyngeal adenoids', 'XPO:0126875', 'abnormally localised aortic arch 5', 0.4166666666666667, 8.127241455820435, 1.8402039578785412, 'HP:0000600', 'Abnormality of the pharynx'),
(109834, 'HP:0040260', 'Decreased size of nasopharyngeal adenoids', 'XPO:0128419', 'decreased size of the pharynx', 0.43820224719101125, 8.872199840740173, 1.971755032386142, 'HP:0033151', 'Abnormal pharynx morphology'),
(109835, 'HP:0040260', 'Decreased size of nasopharyngeal adenoids', 'XPO:0129899', 'increased size of the pharynx', 0.4111111111111111, 8.872199840740173, 1.9098324362431682, 'HP:0033151', 'Abnormal pharynx morphology'),
(109836, 'HP:0040260', 'Decreased size of nasopharyngeal adenoids', 'XPO:0128495', 'decreased size of the aortic arch 2', 0.4017094017094017, 8.872199840740173, 1.8878681336020227, 'HP:0033151', 'Abnormal pharynx morphology'),
(109837, 'HP:0040260', 'Decreased size of nasopharyngeal adenoids', 'XPO:0101474', 'abnormal aortic arch 5', 0.47619047619047616, 8.127241455820435, 1.9672607806191105, 'HP:0000600', 'Abnormality of the pharynx'),
(109838, 'HP:0040260', 'Decreased size of nasopharyngeal adenoids', 'XPO:0125250', 'absent aortic arch 5', 0.40404040404040403, 8.127241455820435, 1.8121075910507107, 'HP:0000600', 'Abnormality of the pharynx'),
(109839, 'HP:0040260', 'Decreased size of nasopharyngeal adenoids', 'XPO:0127194', 'abnormally localised aortic arch 2', 0.4166666666666667, 8.127241455820435, 1.8402039578785412, 'HP:0000600', 'Abnormality of the pharynx'),
(109840, 'HP:0040260', 'Decreased size of nasopharyngeal adenoids', 'XPO:0126957', 'abnormally localised aortic arch 4', 0.4166666666666667, 8.127241455820435, 1.8402039578785412, 'HP:0000600', 'Abnormality of the pharynx'),
(109841, 'HP:0040260', 'Decreased size of nasopharyngeal adenoids', 'XPO:0129453', 'decreased size of the aortic arch 5', 0.40869565217391307, 8.872199840740173, 1.9042136172521698, 'HP:0033151', 'Abnormal pharynx morphology'),
(109842, 'HP:0040260', 'Decreased size of nasopharyngeal adenoids', 'XPO:0129049', 'decreased size of the aortic arch 4', 0.4017094017094017, 8.872199840740173, 1.8878681336020227, 'HP:0033151', 'Abnormal pharynx morphology'),
(109843, 'HP:0040260', 'Decreased size of nasopharyngeal adenoids', 'XPO:0128282', 'decreased size of the aortic arch 6', 0.4017094017094017, 8.872199840740173, 1.8878681336020227, 'HP:0033151', 'Abnormal pharynx morphology'),
(109844, 'HP:0040260', 'Decreased size of nasopharyngeal adenoids', 'XPO:0126876', 'abnormally localised aortic arch', 0.425531914893617, 8.127241455820435, 1.85967755793795, 'HP:0000600', 'Abnormality of the pharynx'),
(109845, 'HP:0040260', 'Decreased size of nasopharyngeal adenoids', 'XPO:0102842', 'abnormal aortic arch 2 morphology', 0.4036697247706422, 8.872199840740173, 1.8924688815993043, 'HP:0033151', 'Abnormal pharynx morphology'),
(109846, 'HP:0040260', 'Decreased size of nasopharyngeal adenoids', 'XPO:0128595', 'decreased size of the aortic arch 3', 0.4017094017094017, 8.872199840740173, 1.8878681336020227, 'HP:0033151', 'Abnormal pharynx morphology'),
(109847, 'HP:0040260', 'Decreased size of nasopharyngeal adenoids', 'XPO:0101748', 'abnormal aortic arch 1 morphology', 0.4036697247706422, 8.872199840740173, 1.8924688815993043, 'HP:0033151', 'Abnormal pharynx morphology'),
(109848, 'HP:0040260', 'Decreased size of nasopharyngeal adenoids', 'XPO:0101395', 'abnormal m. geniohyoideus', 0.41237113402061853, 8.872199840740173, 1.9127569394942936, 'HP:0033151', 'Abnormal pharynx morphology'),
(109849, 'HP:0040260', 'Decreased size of nasopharyngeal adenoids', 'XPO:0140110', 'abnormally necrotic pharynx', 0.4044943820224719, 8.872199840740173, 1.8944009585512962, 'HP:0033151', 'Abnormal pharynx morphology'),
(109850, 'HP:0040260', 'Decreased size of nasopharyngeal adenoids', 'XPO:0101992', 'abnormal aortic arch 6 morphology', 0.4036697247706422, 8.872199840740173, 1.8924688815993043, 'HP:0033151', 'Abnormal pharynx morphology'),
(109851, 'HP:0040260', 'Decreased size of nasopharyngeal adenoids', 'XPO:0128944', 'decreased size of the pharyngeal epithelium', 0.4020618556701031, 8.872199840740173, 1.8886961459811336, 'HP:0033151', 'Abnormal pharynx morphology'),
(109852, 'HP:0040260', 'Decreased size of nasopharyngeal adenoids', 'XPO:0128839', 'decreased size of the aortic arch 1', 0.4017094017094017, 8.872199840740173, 1.8878681336020227, 'HP:0033151', 'Abnormal pharynx morphology'),
(109853, 'HP:0040260', 'Decreased size of nasopharyngeal adenoids', 'XPO:0100116', 'abnormal aortic arch 1', 0.47619047619047616, 8.127241455820435, 1.9672607806191105, 'HP:0000600', 'Abnormality of the pharynx'),
(109854, 'HP:0040260', 'Decreased size of nasopharyngeal adenoids', 'XPO:0100716', 'abnormal aortic arch 3', 0.47619047619047616, 8.127241455820435, 1.9672607806191105, 'HP:0000600', 'Abnormality of the pharynx'),
(109855, 'HP:0040260', 'Decreased size of nasopharyngeal adenoids', 'XPO:0100360', 'abnormal aortic arch 6', 0.47619047619047616, 8.127241455820435, 1.9672607806191105, 'HP:0000600', 'Abnormality of the pharynx'),
(109856, 'HP:0040260', 'Decreased size of nasopharyngeal adenoids', 'XPO:0102668', 'abnormal pharynx morphology', 0.42857142857142855, 8.872199840740173, 1.9499670151869792, 'HP:0033151', 'Abnormal pharynx morphology'),
(109857, 'HP:0040260', 'Decreased size of nasopharyngeal adenoids', 'XPO:0127022', 'abnormally localised aortic arch 3', 0.4166666666666667, 8.127241455820435, 1.8402039578785412, 'HP:0000600', 'Abnormality of the pharynx'),
(109858, 'HP:0040260', 'Decreased size of nasopharyngeal adenoids', 'XPO:0128494', 'decreased size of the oropharynx', 0.4105263157894737, 8.872199840740173, 1.908473608297222, 'HP:0033151', 'Abnormal pharynx morphology'),
(109859, 'HP:0040260', 'Decreased size of nasopharyngeal adenoids', 'XPO:0128496', 'decreased size of the aortic arch', 0.41964285714285715, 8.872199840740173, 1.9295479497308712, 'HP:0033151', 'Abnormal pharynx morphology'),
(109860, 'HP:0040260', 'Decreased size of nasopharyngeal adenoids', 'XPO:0125536', 'absent aortic arch 1', 0.40404040404040403, 8.127241455820435, 1.8121075910507107, 'HP:0000600', 'Abnormality of the pharynx'),
(109861, 'HP:0040260', 'Decreased size of nasopharyngeal adenoids', 'XPO:0126690', 'abnormally localised aortic arch 6', 0.4166666666666667, 8.127241455820435, 1.8402039578785412, 'HP:0000600', 'Abnormality of the pharynx'),
(109862, 'HP:0040260', 'Decreased size of nasopharyngeal adenoids', 'XPO:0102348', 'abnormal aortic arch 3 morphology', 0.4036697247706422, 8.872199840740173, 1.8924688815993043, 'HP:0033151', 'Abnormal pharynx morphology'),
(109863, 'HP:0012583', 'Unilateral renal hypoplasia', 'XPO:0103182', 'abnormal pronephric sinus morphology', 0.40625, 7.603795021646889, 1.7575669909121667, 'HP:0012210', 'Abnormal renal morphology'),
(109864, 'HP:0012583', 'Unilateral renal hypoplasia', 'XPO:0130678', 'increased size of the mesonephric sinus', 0.5094339622641509, 7.603795021646889, 1.968154319691929, 'HP:0012210', 'Abnormal renal morphology'),
(109865, 'HP:0012583', 'Unilateral renal hypoplasia', 'XPO:0101701', 'abnormal urinary system morphology', 0.40816326530612246, 7.340144605965611, 1.730889190615634, 'UPHENO:0087427', 'abnormal renal system morphology'),
(109866, 'HP:0012583', 'Unilateral renal hypoplasia', 'XPO:0128342', 'decreased size of the mesonephric mesenchyme', 0.46774193548387094, 7.603795021646889, 1.8858986718399633, 'HP:0012210', 'Abnormal renal morphology'),
(109867, 'HP:0012583', 'Unilateral renal hypoplasia', 'XPO:0101779', 'abnormal mesonephric mesenchyme morphology', 0.45614035087719296, 7.603795021646889, 1.8623634793380868, 'HP:0012210', 'Abnormal renal morphology'),
(109868, 'HP:0012583', 'Unilateral renal hypoplasia', 'XPO:0102198', 'abnormal kidney morphology', 0.4642857142857143, 7.603795021646889, 1.8789181469418736, 'HP:0012210', 'Abnormal renal morphology'),
(109869, 'HP:0012583', 'Unilateral renal hypoplasia', 'XPO:0129673', 'increased size of the adult kidney', 0.4057971014492754, 12.539624501653302, 2.2557799706605306, 'UPHENO:0075182', 'abnormal size of kidney'),
(109870, 'HP:0012583', 'Unilateral renal hypoplasia', 'XPO:0140815', 'abnormally necrotic mesonephric mesenchyme', 0.4126984126984127, 7.603795021646889, 1.7714610173294143, 'HP:0012210', 'Abnormal renal morphology'),
(109871, 'HP:0012583', 'Unilateral renal hypoplasia', 'XPO:0107388', 'abnormal adult kidney morphology', 0.4482758620689655, 7.603795021646889, 1.8462388167093844, 'HP:0012210', 'Abnormal renal morphology'),
(109872, 'HP:0012583', 'Unilateral renal hypoplasia', 'XPO:0101717', 'abnormal mesonephric sinus morphology', 0.5306122448979592, 7.603795021646889, 2.008647989613905, 'HP:0012210', 'Abnormal renal morphology'),
(109873, 'HP:0012583', 'Unilateral renal hypoplasia', 'XPO:0128275', 'decreased size of the kidney', 0.5, 13.257853533237922, 2.5746702248286013, 'UPHENO:0069110', 'decreased size of the kidney'),
(109874, 'HP:0012583', 'Unilateral renal hypoplasia', 'XPO:0128192', 'decreased size of the mesonephric kidney', 0.4246575342465753, 13.257853533237922, 2.3727720899460745, 'UPHENO:0069110', 'decreased size of the kidney'),
(109875, 'HP:0012583', 'Unilateral renal hypoplasia', 'XPO:0129822', 'increased size of the mesonephric mesenchyme', 0.421875, 7.603795021646889, 1.791047465802423, 'HP:0012210', 'Abnormal renal morphology'),
(109876, 'HP:0012583', 'Unilateral renal hypoplasia', 'XPO:0129755', 'increased size of the kidney', 0.42424242424242425, 12.539624501653302, 2.3064779855162496, 'UPHENO:0075182', 'abnormal size of kidney'),
(109877, 'HP:0012583', 'Unilateral renal hypoplasia', 'XPO:0140552', 'abnormally necrotic kidney', 0.40625, 7.603795021646889, 1.7575669909121667, 'HP:0012210', 'Abnormal renal morphology'),
(109878, 'HP:0012583', 'Unilateral renal hypoplasia', 'XPO:0107387', 'abnormal embryonic kidney morphology', 0.4482758620689655, 7.603795021646889, 1.8462388167093844, 'HP:0012210', 'Abnormal renal morphology'),
(109879, 'HP:0012583', 'Unilateral renal hypoplasia', 'XPO:0128656', 'decreased size of the pronephric nephrostome', 0.4027777777777778, 7.603795021646889, 1.7500399028298366, 'HP:0012210', 'Abnormal renal morphology'),
(109880, 'HP:0012583', 'Unilateral renal hypoplasia', 'XPO:0128197', 'decreased size of the urinary system', 0.4339622641509434, 7.340144605965611, 1.784753700766627, 'UPHENO:0087427', 'abnormal renal system morphology'),
(109881, 'HP:0012583', 'Unilateral renal hypoplasia', 'XPO:0129590', 'increased size of the embryonic kidney', 0.4057971014492754, 12.539624501653302, 2.2557799706605306, 'UPHENO:0075182', 'abnormal size of kidney'),
(109882, 'HP:0012583', 'Unilateral renal hypoplasia', 'XPO:0100085', 'abnormal mesonephric sinus', 0.41304347826086957, 6.880013295263146, 1.685747496500148, 'HP:0000077', 'Abnormality of the kidney'),
(109883, 'HP:0012583', 'Unilateral renal hypoplasia', 'XPO:0128193', 'decreased size of the adult kidney', 0.47692307692307695, 13.257853533237922, 2.5145529026980755, 'UPHENO:0069110', 'decreased size of the kidney'),
(109884, 'HP:0012583', 'Unilateral renal hypoplasia', 'XPO:0128159', 'decreased size of the mesonephric nephron', 0.42028985507246375, 7.603795021646889, 1.7876794756467649, 'HP:0012210', 'Abnormal renal morphology'),
(109885, 'HP:0012583', 'Unilateral renal hypoplasia', 'XPO:0141643', 'neoplastic kidney', 0.4406779661016949, 7.603795021646889, 1.8305258601815884, 'HP:0012210', 'Abnormal renal morphology'),
(109886, 'HP:0012583', 'Unilateral renal hypoplasia', 'XPO:0128110', 'decreased size of the embryonic kidney', 0.47692307692307695, 13.257853533237922, 2.5145529026980755, 'UPHENO:0069110', 'decreased size of the kidney'),
(109887, 'HP:0012583', 'Unilateral renal hypoplasia', 'XPO:0129202', 'decreased size of the mesonephric sinus', 0.5686274509803921, 7.603795021646889, 2.0793572518777204, 'HP:0012210', 'Abnormal renal morphology'),
(109888, 'HP:0012583', 'Unilateral renal hypoplasia', 'XPO:0129375', 'decreased size of the pronephric sinus', 0.4393939393939394, 7.603795021646889, 1.8278570646813308, 'HP:0012210', 'Abnormal renal morphology'),
(109889, 'HP:0012583', 'Unilateral renal hypoplasia', 'XPO:0128461', 'decreased size of the ureter', 0.4166666666666667, 7.340144605965611, 1.7488263452438624, 'UPHENO:0087427', 'abnormal renal system morphology'),
(109890, 'HP:0007002', 'Motor axonal neuropathy', 'XPO:0101204', 'abnormal peripheral nerve', 0.43478260869565216, 7.318748312764234, 1.783834208610917, 'HP:0000759', 'Abnormal peripheral nervous system morphology'),
(109891, 'HP:0007002', 'Motor axonal neuropathy', 'XPO:0101990', 'abnormal ganglion morphology', 0.40384615384615385, 7.318748312764234, 1.7191999177169197, 'HP:0000759', 'Abnormal peripheral nervous system morphology'),
(109892, 'HP:0007002', 'Motor axonal neuropathy', 'XPO:0101807', 'abnormal migrating neuroblast morphology', 0.40425531914893614, 4.7814666189787065, 1.3902997209433732, 'HP:0012639', 'Abnormal nervous system morphology'),
(109893, 'HP:0007002', 'Motor axonal neuropathy', 'XPO:0102747', 'abnormal trunk lateral line morphology', 0.40384615384615385, 7.318748312764234, 1.7191999177169197, 'HP:0000759', 'Abnormal peripheral nervous system morphology'),
(109894, 'HP:0007002', 'Motor axonal neuropathy', 'XPO:0141286', 'abnormal neuron projection morphology', 0.40425531914893614, 4.7814666189787065, 1.3902997209433732, 'HP:0012639', 'Abnormal nervous system morphology'),
(109895, 'HP:0007002', 'Motor axonal neuropathy', 'XPO:0101746', 'abnormal peripheral nervous system morphology', 0.45652173913043476, 7.318748312764234, 1.8278861310270569, 'HP:0000759', 'Abnormal peripheral nervous system morphology'),
(109896, 'HP:0007002', 'Motor axonal neuropathy', 'XPO:0101952', 'abnormal lateral line morphology', 0.42, 7.318748312764234, 1.753246785641137, 'HP:0000759', 'Abnormal peripheral nervous system morphology'),
(109897, 'HP:0007002', 'Motor axonal neuropathy', 'XPO:0102506', 'abnormal occipital lateral line morphology', 0.40384615384615385, 7.318748312764234, 1.7191999177169197, 'HP:0000759', 'Abnormal peripheral nervous system morphology'),
(109898, 'HP:0007002', 'Motor axonal neuropathy', 'XPO:0101030', 'abnormal spinal nerve', 0.4166666666666667, 7.318748312764234, 1.7462755978515432, 'HP:0000759', 'Abnormal peripheral nervous system morphology'),
(109899, 'HP:0007002', 'Motor axonal neuropathy', 'XPO:0101828', 'abnormal neuron morphology', 0.40425531914893614, 4.7814666189787065, 1.3902997209433732, 'HP:0012639', 'Abnormal nervous system morphology'),
(109900, 'HP:0007002', 'Motor axonal neuropathy', 'XPO:0102466', 'abnormal ventral lateral line morphology', 0.40384615384615385, 7.318748312764234, 1.7191999177169197, 'HP:0000759', 'Abnormal peripheral nervous system morphology'),
(109901, 'HP:0007002', 'Motor axonal neuropathy', 'XPO:0102523', 'abnormal dorsal lateral line morphology', 0.40384615384615385, 7.318748312764234, 1.7191999177169197, 'HP:0000759', 'Abnormal peripheral nervous system morphology'),
(109902, 'HP:0007002', 'Motor axonal neuropathy', 'XPO:0102334', 'abnormal glial cell morphology', 0.40425531914893614, 4.7814666189787065, 1.3902997209433732, 'HP:0012639', 'Abnormal nervous system morphology'),
(109903, 'HP:0007002', 'Motor axonal neuropathy', 'XPO:0102670', 'abnormal hyomandibular lateral line morphology', 0.40384615384615385, 7.318748312764234, 1.7191999177169197, 'HP:0000759', 'Abnormal peripheral nervous system morphology'),
(109904, 'HP:0007002', 'Motor axonal neuropathy', 'XPO:0102366', 'abnormal lateral line system morphology', 0.4375, 7.318748312764234, 1.7894000074981424, 'HP:0000759', 'Abnormal peripheral nervous system morphology'),
(109905, 'HP:0007002', 'Motor axonal neuropathy', 'XPO:0103198', 'abnormal posterior lateral line morphology', 0.40384615384615385, 7.318748312764234, 1.7191999177169197, 'HP:0000759', 'Abnormal peripheral nervous system morphology'),
(109906, 'HP:0007002', 'Motor axonal neuropathy', 'XPO:0139791', 'abnormally necrotic peripheral nervous system', 0.40384615384615385, 7.318748312764234, 1.7191999177169197, 'HP:0000759', 'Abnormal peripheral nervous system morphology'),
(109907, 'HP:0007002', 'Motor axonal neuropathy', 'XPO:0133431', 'abnormal cilium morphology in the lateral line', 0.42592592592592593, 7.318748312764234, 1.765572046599321, 'HP:0000759', 'Abnormal peripheral nervous system morphology'),
(109908, 'HP:0007002', 'Motor axonal neuropathy', 'XPO:0102902', 'abnormal caudal lateral line morphology', 0.40384615384615385, 7.318748312764234, 1.7191999177169197, 'HP:0000759', 'Abnormal peripheral nervous system morphology'),
(109909, 'HP:0007002', 'Motor axonal neuropathy', 'XPO:0102995', 'abnormal infraorbital lateral line morphology', 0.40384615384615385, 7.318748312764234, 1.7191999177169197, 'HP:0000759', 'Abnormal peripheral nervous system morphology'),
(109910, 'HP:0007002', 'Motor axonal neuropathy', 'XPO:0101600', 'abnormal Schwann cell', 0.44, 7.318748312764234, 1.7945052960680452, 'HP:0000759', 'Abnormal peripheral nervous system morphology'),
(109911, 'HP:0007002', 'Motor axonal neuropathy', 'XPO:0102326', 'abnormal lateral line primordium morphology', 0.40384615384615385, 7.318748312764234, 1.7191999177169197, 'HP:0000759', 'Abnormal peripheral nervous system morphology'),
(109912, 'HP:0007002', 'Motor axonal neuropathy', 'XPO:0101951', 'abnormal middle lateral line morphology', 0.40384615384615385, 7.318748312764234, 1.7191999177169197, 'HP:0000759', 'Abnormal peripheral nervous system morphology'),
(109913, 'HP:0007002', 'Motor axonal neuropathy', 'XPO:0100167', 'abnormal nerve', 0.43478260869565216, 7.318748312764234, 1.783834208610917, 'HP:0000759', 'Abnormal peripheral nervous system morphology'),
(109914, 'HP:0007002', 'Motor axonal neuropathy', 'XPO:0101960', 'abnormal supraorbital lateral line morphology', 0.40384615384615385, 7.318748312764234, 1.7191999177169197, 'HP:0000759', 'Abnormal peripheral nervous system morphology'),
(109915, 'HP:0001406', 'Intrahepatic cholestasis', 'XPO:0100215', 'abnormal first pancreatic bud', 0.40540540540540543, 5.05060299610679, 1.4309233924911664, 'HP:0025031', 'Abnormality of the digestive system'),
(109916, 'HP:0001406', 'Intrahepatic cholestasis', 'XPO:0141609', 'metaplastic gall bladder', 0.4230769230769231, 9.7042552034261, 2.026239480470839, 'UPHENO:0002666', 'abnormal biliary system'),
(109917, 'HP:0001406', 'Intrahepatic cholestasis', 'XPO:0101536', 'abnormal liver parenchyme', 0.4444444444444444, 7.985637650836012, 1.8839247037130888, 'UPHENO:0003405', 'abnormal liver'),
(109918, 'HP:0001406', 'Intrahepatic cholestasis', 'XPO:0100579', 'abnormal biliary tree', 0.5945945945945946, 9.7042552034261, 2.402102763939051, 'UPHENO:0002666', 'abnormal biliary system'),
(109919, 'HP:0001406', 'Intrahepatic cholestasis', 'XPO:0100890', 'abnormal pharyngeal cavity', 0.45454545454545453, 5.05060299610679, 1.5151662069205463, 'HP:0025031', 'Abnormality of the digestive system'),
(109920, 'HP:0001406', 'Intrahepatic cholestasis', 'XPO:0101381', 'abnormal ventral foregut', 0.42857142857142855, 5.05060299610679, 1.471238981671103, 'HP:0025031', 'Abnormality of the digestive system'),
(109921, 'HP:0001406', 'Intrahepatic cholestasis', 'XPO:0125701', 'absent biliary tree', 0.46808510638297873, 9.7042552034261, 2.131294754195975, 'UPHENO:0002666', 'abnormal biliary system'),
(109922, 'HP:0001406', 'Intrahepatic cholestasis', 'XPO:0100523', 'abnormal midgut', 0.4411764705882353, 5.05060299610679, 1.4927180591674907, 'HP:0025031', 'Abnormality of the digestive system'),
(109923, 'HP:0001406', 'Intrahepatic cholestasis', 'XPO:0100735', 'abnormal hindgut', 0.4411764705882353, 5.05060299610679, 1.4927180591674907, 'HP:0025031', 'Abnormality of the digestive system'),
(109924, 'HP:0001406', 'Intrahepatic cholestasis', 'XPO:0100156', 'abnormal foregut', 0.4411764705882353, 5.05060299610679, 1.4927180591674907, 'HP:0025031', 'Abnormality of the digestive system'),
(109925, 'HP:0001406', 'Intrahepatic cholestasis', 'XPO:0101193', 'abnormal bile duct', 0.5789473684210527, 9.7042552034261, 2.370285428489541, 'UPHENO:0002666', 'abnormal biliary system'),
(109926, 'HP:0001406', 'Intrahepatic cholestasis', 'XPO:0101386', 'abnormal gall bladder', 0.4583333333333333, 9.7042552034261, 2.108976916636033, 'UPHENO:0002666', 'abnormal biliary system'),
(109927, 'HP:0001406', 'Intrahepatic cholestasis', 'XPO:0127346', 'abnormally localised biliary tree', 0.46808510638297873, 9.7042552034261, 2.131294754195975, 'UPHENO:0002666', 'abnormal biliary system'),
(109928, 'HP:0001406', 'Intrahepatic cholestasis', 'XPO:0100621', 'abnormal peritoneum', 0.40540540540540543, 5.05060299610679, 1.4309233924911664, 'HP:0025031', 'Abnormality of the digestive system'),
(109929, 'HP:0001406', 'Intrahepatic cholestasis', 'XPO:0107288', 'abnormal larval alimentary system', 0.46875, 5.05060299610679, 1.5386585568036393, 'HP:0025031', 'Abnormality of the digestive system'),
(109930, 'HP:0001406', 'Intrahepatic cholestasis', 'XPO:0100486', 'abnormal oral evagination', 0.4411764705882353, 5.05060299610679, 1.4927180591674907, 'HP:0025031', 'Abnormality of the digestive system'),
(109931, 'HP:0001406', 'Intrahepatic cholestasis', 'XPO:0125598', 'absent bile duct', 0.44, 9.7042552034261, 2.066366930026583, 'UPHENO:0002666', 'abnormal biliary system'),
(109932, 'HP:0001406', 'Intrahepatic cholestasis', 'XPO:0101198', 'abnormal digestive enzyme secreting cell', 0.40540540540540543, 5.05060299610679, 1.4309233924911664, 'HP:0025031', 'Abnormality of the digestive system'),
(109933, 'HP:0001406', 'Intrahepatic cholestasis', 'XPO:0141617', 'metaplastic liver', 0.425531914893617, 7.985637650836012, 1.8434054576264045, 'UPHENO:0003405', 'abnormal liver'),
(109934, 'HP:0001406', 'Intrahepatic cholestasis', 'XPO:0101601', 'abnormal proctodeum', 0.4166666666666667, 5.05060299610679, 1.45066119926208, 'HP:0025031', 'Abnormality of the digestive system'),
(109935, 'HP:0001406', 'Intrahepatic cholestasis', 'XPO:0100493', 'abnormal liver and biliary system', 0.46875, 5.05060299610679, 1.5386585568036393, 'HP:0025031', 'Abnormality of the digestive system'),
(109936, 'HP:0001406', 'Intrahepatic cholestasis', 'XPO:0101377', 'abnormal manicotto glandulare', 0.4411764705882353, 5.05060299610679, 1.4927180591674907, 'HP:0025031', 'Abnormality of the digestive system'),
(109937, 'HP:0001406', 'Intrahepatic cholestasis', 'XPO:0100152', 'abnormal alimentary system', 0.4838709677419355, 5.05060299610679, 1.5632786569919361, 'HP:0025031', 'Abnormality of the digestive system'),
(109938, 'HP:0001406', 'Intrahepatic cholestasis', 'XPO:0115391', 'abnormally undifferentiated alimentary system', 0.46875, 5.05060299610679, 1.5386585568036393, 'HP:0025031', 'Abnormality of the digestive system'),
(109939, 'HP:0001406', 'Intrahepatic cholestasis', 'XPO:0102211', 'abnormal biliary tree morphology', 0.43137254901960786, 9.7042552034261, 2.0460081386540745, 'UPHENO:0002666', 'abnormal biliary system'),
(109940, 'HP:0001406', 'Intrahepatic cholestasis', 'XPO:0107304', 'abnormal hindgut endoderm', 0.40540540540540543, 5.05060299610679, 1.4309233924911664, 'HP:0025031', 'Abnormality of the digestive system'),
(109941, 'HP:0001406', 'Intrahepatic cholestasis', 'XPO:0102825', 'abnormal bile duct morphology', 0.4230769230769231, 9.7042552034261, 2.026239480470839, 'UPHENO:0002666', 'abnormal biliary system'),
(109942, 'HP:0001406', 'Intrahepatic cholestasis', 'XPO:0142054', 'abnormal digestive tract', 0.45454545454545453, 5.05060299610679, 1.5151662069205463, 'HP:0025031', 'Abnormality of the digestive system'),
(109943, 'HP:0001406', 'Intrahepatic cholestasis', 'XPO:0100986', 'abnormal gut epithelium', 0.42857142857142855, 5.05060299610679, 1.471238981671103, 'HP:0025031', 'Abnormality of the digestive system'),
(109944, 'HP:0001406', 'Intrahepatic cholestasis', 'XPO:0101101', 'abnormal posterior foregut', 0.42857142857142855, 5.05060299610679, 1.471238981671103, 'HP:0025031', 'Abnormality of the digestive system'),
(109945, 'HP:0001406', 'Intrahepatic cholestasis', 'XPO:0100718', 'abnormal ventral pancreatic bud', 0.4166666666666667, 5.05060299610679, 1.45066119926208, 'HP:0025031', 'Abnormality of the digestive system'),
(109946, 'HP:0001406', 'Intrahepatic cholestasis', 'XPO:0100492', 'abnormal gall bladder primordium', 0.40540540540540543, 5.05060299610679, 1.4309233924911664, 'HP:0025031', 'Abnormality of the digestive system'),
(109947, 'HP:0001406', 'Intrahepatic cholestasis', 'XPO:0100462', 'abnormal anterior foregut', 0.42857142857142855, 5.05060299610679, 1.471238981671103, 'HP:0025031', 'Abnormality of the digestive system'),
(109948, 'HP:0001406', 'Intrahepatic cholestasis', 'XPO:0100188', 'abnormal delta cell', 0.4473684210526316, 6.2194654996189955, 1.6680504969442222, 'UPHENO:0003116', 'abnormal endocrine system'),
(109949, 'HP:0001406', 'Intrahepatic cholestasis', 'XPO:0101169', 'abnormal hepato-pancreatic duct', 0.4166666666666667, 5.05060299610679, 1.45066119926208, 'HP:0025031', 'Abnormality of the digestive system'),
(109950, 'HP:0001406', 'Intrahepatic cholestasis', 'XPO:0100225', 'abnormal endocrine system', 0.41935483870967744, 6.2194654996189955, 1.6149807898093176, 'UPHENO:0003116', 'abnormal endocrine system'),
(109951, 'HP:0001406', 'Intrahepatic cholestasis', 'XPO:0100794', 'abnormal liver', 0.46511627906976744, 7.985637650836012, 1.9272389758813733, 'UPHENO:0003405', 'abnormal liver'),
(109952, 'HP:0001406', 'Intrahepatic cholestasis', 'XPO:0127239', 'abnormally localised bile duct', 0.4583333333333333, 9.7042552034261, 2.108976916636033, 'UPHENO:0002666', 'abnormal biliary system'),
(109953, 'HP:0001406', 'Intrahepatic cholestasis', 'XPO:0101021', 'abnormal dorsal foregut', 0.42857142857142855, 5.05060299610679, 1.471238981671103, 'HP:0025031', 'Abnormality of the digestive system'),
(109954, 'HP:0008037', 'Absent anterior chamber of the eye', 'XPO:0127645', 'abnormally localised hyaloid vein', 0.4305555555555556, 6.887869297006056, 1.7220947685207388, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(109955, 'HP:0008037', 'Absent anterior chamber of the eye', 'XPO:0140218', 'abnormally necrotic sclera', 0.4246575342465753, 6.887869297006056, 1.7102589253909142, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(109956, 'HP:0008037', 'Absent anterior chamber of the eye', 'XPO:0103707', 'increased pigmentation in the head', 0.40384615384615385, 4.5318002188002176, 1.3528303989641963, 'UPHENO:0087907', 'abnormal head morphology'),
(109957, 'HP:0008037', 'Absent anterior chamber of the eye', 'XPO:0103022', 'abnormal ciliary body morphology', 0.43243243243243246, 8.412768222102876, 1.907342084098764, 'UPHENO:0087597', 'abnormal anterior segment of eyeball morphology'),
(109958, 'HP:0008037', 'Absent anterior chamber of the eye', 'XPO:0102862', 'abnormal iris morphology', 0.4594594594594595, 9.014833150514745, 2.0351782149120803, 'UPHENO:0021038', 'abnormal anterior segment of eyeball morphology'),
(109959, 'HP:0008037', 'Absent anterior chamber of the eye', 'XPO:0128467', 'decreased size of the lens', 0.4473684210526316, 9.014833150514745, 2.0082210218496126, 'UPHENO:0021038', 'abnormal anterior segment of eyeball morphology'),
(109960, 'HP:0008037', 'Absent anterior chamber of the eye', 'XPO:0140250', 'abnormally necrotic iris', 0.43037974683544306, 9.014833150514745, 1.969721200851099, 'UPHENO:0021038', 'abnormal anterior segment of eyeball morphology'),
(109961, 'HP:0008037', 'Absent anterior chamber of the eye', 'XPO:0101315', 'abnormal hyaloid vascular plexus', 0.5081967213114754, 6.887869297006056, 1.87093361548732, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(109962, 'HP:0008037', 'Absent anterior chamber of the eye', 'XPO:0141323', 'edematous eye', 0.4492753623188406, 6.887869297006056, 1.759133301946505, 'HP:0012372', 'Abnormal eye morphology'),
(109963, 'HP:0008037', 'Absent anterior chamber of the eye', 'XPO:0102212', 'abnormal globe morphology', 0.4090909090909091, 6.575878401988876, 1.640162209521029, 'UPHENO:0087924', 'abnormal camera-type eye morphology'),
(109964, 'HP:0008037', 'Absent anterior chamber of the eye', 'XPO:0102117', 'abnormal retina morphology', 0.4189189189189189, 6.887869297006056, 1.6986638159319787, 'HP:0012372', 'Abnormal eye morphology'),
(109965, 'HP:0008037', 'Absent anterior chamber of the eye', 'XPO:0133371', 'eye fused with olfactory pit', 0.44285714285714284, 6.887869297006056, 1.7465228647932265, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(109966, 'HP:0008037', 'Absent anterior chamber of the eye', 'XPO:0129419', 'decreased size of the pupil', 0.425, 9.014833150514745, 1.957371729889028, 'UPHENO:0021038', 'abnormal anterior segment of eyeball morphology'),
(109967, 'HP:0008037', 'Absent anterior chamber of the eye', 'XPO:0103048', 'abnormal cornea morphology', 0.4722222222222222, 9.014833150514745, 2.0632509646910697, 'UPHENO:0021038', 'abnormal anterior segment of eyeball morphology'),
(109968, 'HP:0008037', 'Absent anterior chamber of the eye', 'XPO:0141638', 'neoplastic eye', 0.44285714285714284, 6.887869297006056, 1.7465228647932265, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(109969, 'HP:0008037', 'Absent anterior chamber of the eye', 'XPO:0101823', 'abnormal lens epithelium morphology', 0.44155844155844154, 9.014833150514745, 1.9951380094746995, 'UPHENO:0021038', 'abnormal anterior segment of eyeball morphology'),
(109970, 'HP:0008037', 'Absent anterior chamber of the eye', 'XPO:0101634', 'abnormal head morphology', 0.42857142857142855, 4.5318002188002176, 1.3936283915633758, 'UPHENO:0087907', 'abnormal head morphology'),
(109971, 'HP:0008037', 'Absent anterior chamber of the eye', 'XPO:0101359', 'abnormal hyaloid artery', 0.41333333333333333, 6.887869297006056, 1.6873013886368484, 'HP:0012372', 'Abnormal eye morphology'),
(109972, 'HP:0008037', 'Absent anterior chamber of the eye', 'XPO:0133354', 'fused eyes', 0.44285714285714284, 6.887869297006056, 1.7465228647932265, 'HP:0012372', 'Abnormal eye morphology'),
(109973, 'HP:0008037', 'Absent anterior chamber of the eye', 'XPO:0102538', 'abnormal lateral nasal prominence morphology', 0.40384615384615385, 4.5318002188002176, 1.3528303989641963, 'UPHENO:0087907', 'abnormal head morphology'),
(109974, 'HP:0008037', 'Absent anterior chamber of the eye', 'XPO:0100371', 'abnormal hyaloid blood vessel', 0.5254237288135594, 6.887869297006056, 1.9023800802188169, 'HP:0012372', 'Abnormal eye morphology'),
(109975, 'HP:0008037', 'Absent anterior chamber of the eye', 'XPO:0139731', 'abnormally necrotic eye', 0.4189189189189189, 6.887869297006056, 1.6986638159319787, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(109976, 'HP:0008037', 'Absent anterior chamber of the eye', 'XPO:0130285', 'increased size of the lens transitional zone', 0.44155844155844154, 9.014833150514745, 1.9951380094746995, 'UPHENO:0021038', 'abnormal anterior segment of eyeball morphology'),
(109977, 'HP:0008037', 'Absent anterior chamber of the eye', 'XPO:0141298', 'abnormal intercanthal region morphology', 0.4117647058823529, 4.5318002188002176, 1.3660290568695288, 'UPHENO:0087907', 'abnormal head morphology'),
(109978, 'HP:0008037', 'Absent anterior chamber of the eye', 'XPO:0140335', 'abnormally necrotic pharyngeal region', 0.4117647058823529, 4.5318002188002176, 1.3660290568695288, 'UPHENO:0087907', 'abnormal head morphology'),
(109979, 'HP:0008037', 'Absent anterior chamber of the eye', 'XPO:0102196', 'abnormal central retina morphology', 0.4189189189189189, 6.887869297006056, 1.6986638159319787, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(109980, 'HP:0008037', 'Absent anterior chamber of the eye', 'XPO:0141337', 'increased pigmentation in the eye', 0.44285714285714284, 6.887869297006056, 1.7465228647932265, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(109981, 'HP:0008037', 'Absent anterior chamber of the eye', 'XPO:0103101', 'abnormal medial nasal prominence morphology', 0.40384615384615385, 4.5318002188002176, 1.3528303989641963, 'UPHENO:0087907', 'abnormal head morphology'),
(109982, 'HP:0008037', 'Absent anterior chamber of the eye', 'XPO:0100710', 'abnormal hyaloid vein', 0.5081967213114754, 6.887869297006056, 1.87093361548732, 'HP:0012372', 'Abnormal eye morphology'),
(109983, 'HP:0008037', 'Absent anterior chamber of the eye', 'XPO:0115417', 'abnormally wholly ventralized eye', 0.4189189189189189, 6.887869297006056, 1.6986638159319787, 'HP:0012372', 'Abnormal eye morphology'),
(109984, 'HP:0008037', 'Absent anterior chamber of the eye', 'XPO:0127907', 'abnormally localised optic choroid vascular plexus', 0.43661971830985913, 6.887869297006056, 1.734179792355427, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(109985, 'HP:0008037', 'Absent anterior chamber of the eye', 'XPO:0142059', 'abnormal nasal region morphology', 0.42, 4.5318002188002176, 1.3796217205799897, 'UPHENO:0087907', 'abnormal head morphology'),
(109986, 'HP:0008037', 'Absent anterior chamber of the eye', 'XPO:0141835', 'edematous head', 0.4117647058823529, 4.5318002188002176, 1.3660290568695288, 'UPHENO:0087907', 'abnormal head morphology'),
(109987, 'HP:0008037', 'Absent anterior chamber of the eye', 'XPO:0100329', 'abnormal retinal blood vessel', 0.4246575342465753, 6.887869297006056, 1.7102589253909142, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(109988, 'HP:0008037', 'Absent anterior chamber of the eye', 'XPO:0103110', 'abnormal lens fiber cell mass morphology', 0.425, 9.014833150514745, 1.957371729889028, 'UPHENO:0021038', 'abnormal anterior segment of eyeball morphology'),
(109989, 'HP:0008037', 'Absent anterior chamber of the eye', 'XPO:0115423', 'abnormally incomplete structure of eye', 0.45588235294117646, 6.887869297006056, 1.7720208976957377, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(109990, 'HP:0008037', 'Absent anterior chamber of the eye', 'XPO:0141839', 'edematous pharyngeal region', 0.42, 4.5318002188002176, 1.3796217205799897, 'UPHENO:0087907', 'abnormal head morphology'),
(109991, 'HP:0008037', 'Absent anterior chamber of the eye', 'XPO:0126243', 'absent optic choroid vascular plexus', 0.40789473684210525, 6.887869297006056, 1.6761639640277146, 'HP:0012372', 'Abnormal eye morphology'),
(109992, 'HP:0008037', 'Absent anterior chamber of the eye', 'XPO:0128052', 'decreased size of the iris', 0.41975308641975306, 9.014833150514745, 1.9452516645636548, 'UPHENO:0021038', 'abnormal anterior segment of eyeball morphology'),
(109993, 'HP:0008037', 'Absent anterior chamber of the eye', 'XPO:0100779', 'abnormal optic choroid vascular plexus', 0.5166666666666667, 6.887869297006056, 1.886460301760892, 'HP:0012372', 'Abnormal eye morphology'),
(109994, 'HP:0008037', 'Absent anterior chamber of the eye', 'XPO:0102550', 'abnormal lens morphology', 0.5, 9.014833150514745, 2.1230677274306093, 'UPHENO:0021038', 'abnormal anterior segment of eyeball morphology'),
(109995, 'HP:0008037', 'Absent anterior chamber of the eye', 'XPO:0127783', 'abnormally localised hyaloid vascular plexus', 0.4246575342465753, 6.887869297006056, 1.7102589253909142, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(109996, 'HP:0008037', 'Absent anterior chamber of the eye', 'XPO:0140375', 'abnormally necrotic lens', 0.4657534246575342, 9.014833150514745, 2.0490703776514145, 'UPHENO:0021038', 'abnormal anterior segment of eyeball morphology'),
(109997, 'HP:0008037', 'Absent anterior chamber of the eye', 'XPO:0102804', 'abnormal pharyngeal pouch morphology', 0.40384615384615385, 4.5318002188002176, 1.3528303989641963, 'UPHENO:0087907', 'abnormal head morphology'),
(109998, 'HP:0008037', 'Absent anterior chamber of the eye', 'XPO:0140538', 'abnormally necrotic optic disc', 0.40298507462686567, 6.575878401988876, 1.6278761772821302, 'UPHENO:0087924', 'abnormal camera-type eye morphology'),
(109999, 'HP:0008037', 'Absent anterior chamber of the eye', 'XPO:0102734', 'abnormal craniofacial region morphology', 0.40384615384615385, 4.5318002188002176, 1.3528303989641963, 'UPHENO:0087907', 'abnormal head morphology'),
(110000, 'HP:0008037', 'Absent anterior chamber of the eye', 'XPO:0129532', 'increased size of the iris', 0.41975308641975306, 9.014833150514745, 1.9452516645636548, 'UPHENO:0021038', 'abnormal anterior segment of eyeball morphology'),
(110001, 'HP:0008037', 'Absent anterior chamber of the eye', 'XPO:0129947', 'increased size of the lens', 0.4473684210526316, 9.014833150514745, 2.0082210218496126, 'UPHENO:0021038', 'abnormal anterior segment of eyeball morphology'),
(110002, 'HP:0008037', 'Absent anterior chamber of the eye', 'XPO:0100420', 'abnormal choana', 0.42105263157894735, 5.788671267106304, 1.561196743002159, 'UPHENO:0087472', 'abnormal face morphology'),
(110003, 'HP:0008037', 'Absent anterior chamber of the eye', 'XPO:0101817', 'abnormal eye morphology', 0.4626865671641791, 6.887869297006056, 1.7851959556606887, 'HP:0012372', 'Abnormal eye morphology'),
(110004, 'HP:0008037', 'Absent anterior chamber of the eye', 'XPO:0133372', 'eye fused with olfactory epithelium', 0.44285714285714284, 6.887869297006056, 1.7465228647932265, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(110005, 'HP:0008037', 'Absent anterior chamber of the eye', 'XPO:0141339', 'decreased pigmentation in the head', 0.40384615384615385, 4.5318002188002176, 1.3528303989641963, 'UPHENO:0087907', 'abnormal head morphology'),
(110006, 'HP:0008037', 'Absent anterior chamber of the eye', 'XPO:0129388', 'decreased size of the sclera', 0.41333333333333333, 6.887869297006056, 1.6873013886368484, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(110007, 'HP:0008037', 'Absent anterior chamber of the eye', 'XPO:0102513', 'abnormal sclera morphology', 0.45588235294117646, 6.887869297006056, 1.7720208976957377, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(110008, 'HP:0008037', 'Absent anterior chamber of the eye', 'XPO:0102003', 'abnormal hyaloid blood vessel morphology', 0.4305555555555556, 6.887869297006056, 1.7220947685207388, 'HP:0012372', 'Abnormal eye morphology'),
(110009, 'HP:0008037', 'Absent anterior chamber of the eye', 'XPO:0125990', 'absent hyaloid vein', 0.41333333333333333, 6.887869297006056, 1.6873013886368484, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(110010, 'HP:0008037', 'Absent anterior chamber of the eye', 'XPO:0141343', 'decreased pigmentation in the eye', 0.44285714285714284, 6.887869297006056, 1.7465228647932265, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(110011, 'HP:0008037', 'Absent anterior chamber of the eye', 'XPO:0115526', 'abnormally incomplete structure of head', 0.42, 4.5318002188002176, 1.3796217205799897, 'UPHENO:0087907', 'abnormal head morphology'),
(110012, 'HP:0008037', 'Absent anterior chamber of the eye', 'XPO:0125589', 'absent hyaloid blood vessel', 0.43661971830985913, 6.887869297006056, 1.734179792355427, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(110013, 'HP:0008037', 'Absent anterior chamber of the eye', 'XPO:0103210', 'abnormal pupil morphology', 0.4594594594594595, 9.014833150514745, 2.0351782149120803, 'UPHENO:0021038', 'abnormal anterior segment of eyeball morphology'),
(110014, 'HP:0008037', 'Absent anterior chamber of the eye', 'XPO:0101483', 'abnormal nostril', 0.43636363636363634, 5.788671267106304, 1.589328677092377, 'UPHENO:0087472', 'abnormal face morphology'),
(110015, 'HP:0008037', 'Absent anterior chamber of the eye', 'XPO:0130863', 'increased size of the sclera', 0.41333333333333333, 6.887869297006056, 1.6873013886368484, 'HP:0012372', 'Abnormal eye morphology'),
(110016, 'HP:0008037', 'Absent anterior chamber of the eye', 'XPO:0102476', 'abnormal lens transitional zone morphology', 0.4857142857142857, 9.014833150514745, 2.0925183976576487, 'UPHENO:0021038', 'abnormal anterior segment of eyeball morphology'),
(110017, 'HP:0008037', 'Absent anterior chamber of the eye', 'XPO:0128807', 'decreased size of the lens transitional zone', 0.44155844155844154, 9.014833150514745, 1.9951380094746995, 'UPHENO:0021038', 'abnormal anterior segment of eyeball morphology'),
(110018, 'HP:0008037', 'Absent anterior chamber of the eye', 'XPO:0127230', 'abnormally localised hyaloid blood vessel', 0.45588235294117646, 6.887869297006056, 1.7720208976957377, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(110019, 'HP:0008037', 'Absent anterior chamber of the eye', 'XPO:0126122', 'absent hyaloid vascular plexus', 0.40789473684210525, 6.887869297006056, 1.6761639640277146, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(110020, 'HP:0008037', 'Absent anterior chamber of the eye', 'XPO:0140391', 'abnormally necrotic central retina', 0.4025974025974026, 6.887869297006056, 1.6652442128423794, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(110021, 'HP:0008037', 'Absent anterior chamber of the eye', 'XPO:0103186', 'abnormal peripheral retina morphology', 0.4025974025974026, 6.887869297006056, 1.6652442128423794, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(110022, 'HP:0008037', 'Absent anterior chamber of the eye', 'XPO:0102831', 'abnormal optic disc morphology', 0.421875, 6.575878401988876, 1.6655925974976766, 'UPHENO:0087924', 'abnormal camera-type eye morphology'),
(110023, 'HP:0008037', 'Absent anterior chamber of the eye', 'XPO:0129260', 'decreased size of the cornea', 0.40476190476190477, 9.014833150514745, 1.910199213986099, 'UPHENO:0021038', 'abnormal anterior segment of eyeball morphology'),
(110024, 'HP:0008037', 'Absent anterior chamber of the eye', 'XPO:0130893', 'increased size of the pupil', 0.43037974683544306, 9.014833150514745, 1.969721200851099, 'UPHENO:0021038', 'abnormal anterior segment of eyeball morphology'),
(110025, 'HP:0008037', 'Absent anterior chamber of the eye', 'XPO:0130736', 'increased size of the cornea', 0.40476190476190477, 9.014833150514745, 1.910199213986099, 'UPHENO:0021038', 'abnormal anterior segment of eyeball morphology'),
(110026, 'HP:0008037', 'Absent anterior chamber of the eye', 'XPO:0133369', 'eye fused with brain', 0.44285714285714284, 6.887869297006056, 1.7465228647932265, 'HP:0012372', 'Abnormal eye morphology'),
(110027, 'HP:0008037', 'Absent anterior chamber of the eye', 'XPO:0102805', 'abnormal retinal layer morphology', 0.4305555555555556, 6.887869297006056, 1.7220947685207388, 'HP:0012372', 'Abnormal eye morphology'),
(110028, 'HP:0008037', 'Absent anterior chamber of the eye', 'XPO:0140473', 'abnormally necrotic lens transitional zone', 0.4533333333333333, 9.014833150514745, 2.021564829919309, 'UPHENO:0021038', 'abnormal anterior segment of eyeball morphology'),
(110029, 'HP:0008037', 'Absent anterior chamber of the eye', 'XPO:0102259', 'abnormal pharyngeal region morphology', 0.4375, 4.5318002188002176, 1.4080705222839853, 'UPHENO:0087907', 'abnormal head morphology'),
(110030, 'HP:0008037', 'Absent anterior chamber of the eye', 'XPO:0141141', 'abnormally necrotic cornea', 0.4358974358974359, 9.014833150514745, 1.982307406875276, 'UPHENO:0021038', 'abnormal anterior segment of eyeball morphology'),
(110031, 'HP:0025516', 'Coronary-pulmonary artery fistula', 'XPO:0102683', 'abnormal intersomitic vein morphology', 0.4067796610169492, 6.974839882869777, 1.6844058309093048, 'UPHENO:0087186', 'abnormal blood vessel morphology'),
(110032, 'HP:0025516', 'Coronary-pulmonary artery fistula', 'XPO:0102838', 'abnormal ischiadic vein morphology', 0.43103448275862066, 7.803720102857406, 1.8340317494875034, 'HP:0033353', 'Abnormal blood vessel morphology'),
(110033, 'HP:0025516', 'Coronary-pulmonary artery fistula', 'XPO:0101711', 'abnormal dorsal aorta morphology', 0.43283582089552236, 9.08792853179561, 1.9833257438705303, 'UPHENO:0087334', 'abnormal systemic artery morphology'),
(110034, 'HP:0025516', 'Coronary-pulmonary artery fistula', 'XPO:0140152', 'abnormally necrotic capillary', 0.4032258064516129, 7.803720102857406, 1.7738831223610367, 'HP:0033353', 'Abnormal blood vessel morphology'),
(110035, 'HP:0025516', 'Coronary-pulmonary artery fistula', 'XPO:0102424', 'abnormal capillary morphology', 0.44642857142857145, 7.803720102857406, 1.86649500865849, 'HP:0033353', 'Abnormal blood vessel morphology'),
(110036, 'HP:0025516', 'Coronary-pulmonary artery fistula', 'XPO:0128030', 'decreased size of the blood vessel', 0.41379310344827586, 6.974839882869777, 1.6988645152534954, 'UPHENO:0087186', 'abnormal blood vessel morphology'),
(110037, 'HP:0025516', 'Coronary-pulmonary artery fistula', 'XPO:0101686', 'abnormal blood vessel morphology', 0.47058823529411764, 6.974839882869777, 1.8117057133924146, 'UPHENO:0087186', 'abnormal blood vessel morphology'),
(110038, 'HP:0025516', 'Coronary-pulmonary artery fistula', 'XPO:0101708', 'abnormal artery morphology', 0.46296296296296297, 8.244823584788804, 1.9537266840376477, 'UPHENO:0086797', 'abnormal artery morphology'),
(110039, 'HP:0025516', 'Coronary-pulmonary artery fistula', 'XPO:0102613', 'abnormal dorsal longitudinal anastomosing vessel morphology', 0.4528301886792453, 6.974839882869777, 1.7771938724200707, 'UPHENO:0087186', 'abnormal blood vessel morphology'),
(110040, 'HP:0025516', 'Coronary-pulmonary artery fistula', 'XPO:0139723', 'abnormally necrotic blood vessel', 0.42857142857142855, 6.974839882869777, 1.7289352482549702, 'UPHENO:0087186', 'abnormal blood vessel morphology'),
(110041, 'HP:0025516', 'Coronary-pulmonary artery fistula', 'XPO:0103063', 'abnormal ischiadic artery morphology', 0.44642857142857145, 8.244823584788804, 1.9185215178980555, 'UPHENO:0086797', 'abnormal artery morphology'),
(110042, 'HP:0025516', 'Coronary-pulmonary artery fistula', 'XPO:0139828', 'abnormally necrotic paired dorsal aorta', 0.4142857142857143, 9.08792853179561, 1.9403605240193038, 'UPHENO:0087334', 'abnormal systemic artery morphology'),
(110043, 'HP:0025516', 'Coronary-pulmonary artery fistula', 'XPO:0103119', 'abnormal epigastric artery morphology', 0.4098360655737705, 8.244823584788804, 1.838212735060791, 'UPHENO:0086797', 'abnormal artery morphology'),
(110044, 'HP:0025516', 'Coronary-pulmonary artery fistula', 'XPO:0102565', 'abnormal branchial vein morphology', 0.43103448275862066, 7.803720102857406, 1.8340317494875034, 'HP:0033353', 'Abnormal blood vessel morphology'),
(110045, 'HP:0025516', 'Coronary-pulmonary artery fistula', 'XPO:0102612', 'abnormal dorsal longitudinal anastomosing vessel - left branch morphology', 0.43636363636363634, 6.974839882869777, 1.744582040015079, 'UPHENO:0087186', 'abnormal blood vessel morphology'),
(110046, 'HP:0025516', 'Coronary-pulmonary artery fistula', 'XPO:0101780', 'abnormal arteria mesenterica posterior morphology', 0.43283582089552236, 9.08792853179561, 1.9833257438705303, 'UPHENO:0087334', 'abnormal systemic artery morphology'),
(110047, 'HP:0025516', 'Coronary-pulmonary artery fistula', 'XPO:0128093', 'decreased size of the aorta', 0.42028985507246375, 9.08792853179561, 1.9543705292337186, 'UPHENO:0087334', 'abnormal systemic artery morphology'),
(110048, 'HP:0025516', 'Coronary-pulmonary artery fistula', 'XPO:0139829', 'abnormally necrotic artery', 0.4166666666666667, 8.244823584788804, 1.8534678741021298, 'UPHENO:0086797', 'abnormal artery morphology'),
(110049, 'HP:0025516', 'Coronary-pulmonary artery fistula', 'XPO:0101840', 'abnormal ventral aorta morphology', 0.43283582089552236, 9.08792853179561, 1.9833257438705303, 'UPHENO:0087334', 'abnormal systemic artery morphology'),
(110050, 'HP:0025516', 'Coronary-pulmonary artery fistula', 'XPO:0103217', 'abnormal dorsal longitudinal anastomosing vessel - right branch morphology', 0.43636363636363634, 6.974839882869777, 1.744582040015079, 'UPHENO:0087186', 'abnormal blood vessel morphology'),
(110051, 'HP:0025516', 'Coronary-pulmonary artery fistula', 'XPO:0102619', 'abnormal larval aorta morphology', 0.44642857142857145, 8.244823584788804, 1.9185215178980555, 'UPHENO:0086797', 'abnormal artery morphology'),
(110052, 'HP:0025516', 'Coronary-pulmonary artery fistula', 'XPO:0129573', 'increased size of the aorta', 0.42028985507246375, 9.08792853179561, 1.9543705292337186, 'UPHENO:0087334', 'abnormal systemic artery morphology'),
(110053, 'HP:0025516', 'Coronary-pulmonary artery fistula', 'XPO:0102311', 'abnormal left channel of ventral aorta morphology', 0.4098360655737705, 8.244823584788804, 1.838212735060791, 'UPHENO:0086797', 'abnormal artery morphology'),
(110054, 'HP:0025516', 'Coronary-pulmonary artery fistula', 'XPO:0101769', 'abnormal cardinal vein morphology', 0.4166666666666667, 7.803720102857406, 1.8032054910234865, 'HP:0033353', 'Abnormal blood vessel morphology'),
(110055, 'HP:0025516', 'Coronary-pulmonary artery fistula', 'XPO:0140595', 'abnormally necrotic dorsal longitudinal anastomosing vessel', 0.4067796610169492, 6.974839882869777, 1.6844058309093048, 'UPHENO:0087186', 'abnormal blood vessel morphology'),
(110056, 'HP:0025516', 'Coronary-pulmonary artery fistula', 'XPO:0101956', 'abnormal intersomitic vessel morphology', 0.42105263157894735, 6.974839882869777, 1.7137020416408788, 'UPHENO:0087186', 'abnormal blood vessel morphology'),
(110057, 'HP:0025516', 'Coronary-pulmonary artery fistula', 'XPO:0102802', 'abnormal arteria subclavia morphology', 0.41935483870967744, 9.08792853179561, 1.9521953805027363, 'UPHENO:0087334', 'abnormal systemic artery morphology'),
(110058, 'HP:0025516', 'Coronary-pulmonary artery fistula', 'XPO:0103091', 'abnormal arteria iliaca communis morphology', 0.4461538461538462, 9.08792853179561, 2.0136072775076794, 'UPHENO:0087334', 'abnormal systemic artery morphology'),
(110059, 'HP:0025516', 'Coronary-pulmonary artery fistula', 'XPO:0101774', 'abnormal paired dorsal aorta morphology', 0.46774193548387094, 9.08792853179561, 2.061748112888956, 'UPHENO:0087334', 'abnormal systemic artery morphology'),
(110060, 'HP:0025516', 'Coronary-pulmonary artery fistula', 'XPO:0101916', 'abnormal tail vasculature morphology', 0.4067796610169492, 6.974839882869777, 1.6844058309093048, 'UPHENO:0087186', 'abnormal blood vessel morphology'),
(110061, 'HP:0025516', 'Coronary-pulmonary artery fistula', 'XPO:0127366', 'abnormally localised external carotid artery', 0.4027777777777778, 9.08792853179561, 1.91322127801253, 'UPHENO:0087334', 'abnormal systemic artery morphology'),
(110062, 'HP:0025516', 'Coronary-pulmonary artery fistula', 'XPO:0102412', 'abnormal vascular plexus morphology', 0.4444444444444444, 6.974839882869777, 1.7606614770679263, 'UPHENO:0087186', 'abnormal blood vessel morphology'),
(110063, 'HP:0025516', 'Coronary-pulmonary artery fistula', 'XPO:0128092', 'decreased size of the paired dorsal aorta', 0.4027777777777778, 9.08792853179561, 1.91322127801253, 'UPHENO:0087334', 'abnormal systemic artery morphology'),
(110064, 'HP:0025516', 'Coronary-pulmonary artery fistula', 'XPO:0101154', 'abnormal external carotid artery', 0.46774193548387094, 9.08792853179561, 2.061748112888956, 'UPHENO:0087334', 'abnormal systemic artery morphology'),
(110065, 'HP:0025516', 'Coronary-pulmonary artery fistula', 'XPO:0103189', 'abnormal Jacobsons vein morphology', 0.43103448275862066, 7.803720102857406, 1.8340317494875034, 'HP:0033353', 'Abnormal blood vessel morphology'),
(110066, 'HP:0025516', 'Coronary-pulmonary artery fistula', 'XPO:0139803', 'abnormally necrotic aorta', 0.43283582089552236, 9.08792853179561, 1.9833257438705303, 'UPHENO:0087334', 'abnormal systemic artery morphology'),
(110067, 'HP:0025516', 'Coronary-pulmonary artery fistula', 'XPO:0102329', 'abnormal caudal artery morphology', 0.4393939393939394, 9.08792853179561, 1.9982944524059143, 'UPHENO:0087334', 'abnormal systemic artery morphology'),
(110068, 'HP:0025516', 'Coronary-pulmonary artery fistula', 'XPO:0102875', 'abnormal vertebral artery morphology', 0.44642857142857145, 8.244823584788804, 1.9185215178980555, 'UPHENO:0086797', 'abnormal artery morphology'),
(110069, 'HP:0025516', 'Coronary-pulmonary artery fistula', 'XPO:0101052', 'abnormal ophthalmic artery', 0.4084507042253521, 9.08792853179561, 1.9266475569656187, 'UPHENO:0087334', 'abnormal systemic artery morphology'),
(110070, 'HP:0025516', 'Coronary-pulmonary artery fistula', 'XPO:0101712', 'abnormal aorta morphology', 0.48333333333333334, 9.08792853179561, 2.095828902932651, 'UPHENO:0087334', 'abnormal systemic artery morphology'),
(110071, 'HP:0025516', 'Coronary-pulmonary artery fistula', 'XPO:0101675', 'abnormal vein morphology', 0.44642857142857145, 7.803720102857406, 1.86649500865849, 'HP:0033353', 'Abnormal blood vessel morphology'),
(110072, 'HP:0025516', 'Coronary-pulmonary artery fistula', 'XPO:0141554', 'abnormal blood vessel morphology in the regenerating hindlimb', 0.42105263157894735, 6.974839882869777, 1.7137020416408788, 'UPHENO:0087186', 'abnormal blood vessel morphology'),
(110073, 'HP:0025516', 'Coronary-pulmonary artery fistula', 'XPO:0128099', 'decreased size of the artery', 0.4032258064516129, 8.244823584788804, 1.8233281764476037, 'UPHENO:0086797', 'abnormal artery morphology'),
(110074, 'HP:0025516', 'Coronary-pulmonary artery fistula', 'XPO:0129572', 'increased size of the paired dorsal aorta', 0.4027777777777778, 9.08792853179561, 1.91322127801253, 'UPHENO:0087334', 'abnormal systemic artery morphology'),
(110075, 'HP:0025516', 'Coronary-pulmonary artery fistula', 'XPO:0102154', 'abnormal subinterstitial vein morphology', 0.43103448275862066, 7.803720102857406, 1.8340317494875034, 'HP:0033353', 'Abnormal blood vessel morphology'),
(110076, 'HP:0025516', 'Coronary-pulmonary artery fistula', 'XPO:0140757', 'abnormally necrotic arteria iliaca communis', 0.4027777777777778, 9.08792853179561, 1.91322127801253, 'UPHENO:0087334', 'abnormal systemic artery morphology'),
(110077, 'HP:0025516', 'Coronary-pulmonary artery fistula', 'XPO:0102421', 'abnormal occipitovertebral artery morphology', 0.44642857142857145, 8.244823584788804, 1.9185215178980555, 'UPHENO:0086797', 'abnormal artery morphology'),
(110078, 'HP:0025516', 'Coronary-pulmonary artery fistula', 'XPO:0129510', 'increased size of the blood vessel', 0.41379310344827586, 6.974839882869777, 1.6988645152534954, 'UPHENO:0087186', 'abnormal blood vessel morphology'),
(110079, 'HP:0025516', 'Coronary-pulmonary artery fistula', 'XPO:0103215', 'abnormal truncus arteriosus morphology', 0.4528301886792453, 6.974839882869777, 1.7771938724200707, 'UPHENO:0087186', 'abnormal blood vessel morphology'),
(110080, 'HP:0025516', 'Coronary-pulmonary artery fistula', 'XPO:0102889', 'abnormal coeliaco-mesenteric artery morphology', 0.4098360655737705, 8.244823584788804, 1.838212735060791, 'UPHENO:0086797', 'abnormal artery morphology'),
(110081, 'HP:0025516', 'Coronary-pulmonary artery fistula', 'XPO:0129579', 'increased size of the artery', 0.4032258064516129, 8.244823584788804, 1.8233281764476037, 'UPHENO:0086797', 'abnormal artery morphology'),
(110082, 'HP:0025516', 'Coronary-pulmonary artery fistula', 'XPO:0101845', 'abnormal right channel of ventral aorta morphology', 0.4098360655737705, 8.244823584788804, 1.838212735060791, 'UPHENO:0086797', 'abnormal artery morphology'),
(110083, 'HP:0025516', 'Coronary-pulmonary artery fistula', 'XPO:0140809', 'abnormally necrotic truncus arteriosus', 0.4067796610169492, 6.974839882869777, 1.6844058309093048, 'UPHENO:0087186', 'abnormal blood vessel morphology'),
(110084, 'HP:0025516', 'Coronary-pulmonary artery fistula', 'XPO:0139730', 'abnormally necrotic vein', 0.4032258064516129, 7.803720102857406, 1.7738831223610367, 'HP:0033353', 'Abnormal blood vessel morphology'),
(110085, 'HP:0000495', 'Recurrent corneal erosions', 'XPO:0141141', 'abnormally necrotic cornea', 0.4810126582278481, 10.582693223545188, 2.256193564095799, 'UPHENO:0020998', 'abnormal cornea morphology'),
(110086, 'HP:0000495', 'Recurrent corneal erosions', 'XPO:0101315', 'abnormal hyaloid vascular plexus', 0.4696969696969697, 6.887869297006056, 1.7986693238259617, 'HP:0012372', 'Abnormal eye morphology'),
(110087, 'HP:0000495', 'Recurrent corneal erosions', 'XPO:0133354', 'fused eyes', 0.41333333333333333, 6.887869297006056, 1.6873013886368484, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(110088, 'HP:0000495', 'Recurrent corneal erosions', 'XPO:0102476', 'abnormal lens transitional zone morphology', 0.4533333333333333, 9.014833150514745, 2.021564829919309, 'UPHENO:0021038', 'abnormal anterior segment of eyeball morphology'),
(110089, 'HP:0000495', 'Recurrent corneal erosions', 'XPO:0103022', 'abnormal ciliary body morphology', 0.4050632911392405, 8.412768222102876, 1.8459966369515974, 'UPHENO:0087597', 'abnormal anterior segment of eyeball morphology'),
(110090, 'HP:0000495', 'Recurrent corneal erosions', 'XPO:0100779', 'abnormal optic choroid vascular plexus', 0.47692307692307695, 6.887869297006056, 1.8124524320853552, 'HP:0012372', 'Abnormal eye morphology'),
(110091, 'HP:0000495', 'Recurrent corneal erosions', 'XPO:0127907', 'abnormally localised optic choroid vascular plexus', 0.40789473684210525, 6.887869297006056, 1.6761639640277146, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(110092, 'HP:0000495', 'Recurrent corneal erosions', 'XPO:0103048', 'abnormal cornea morphology', 0.5205479452054794, 10.582693223545188, 2.347083128535587, 'UPHENO:0020998', 'abnormal cornea morphology'),
(110093, 'HP:0000495', 'Recurrent corneal erosions', 'XPO:0103210', 'abnormal pupil morphology', 0.43037974683544306, 9.014833150514745, 1.969721200851099, 'UPHENO:0021038', 'abnormal anterior segment of eyeball morphology'),
(110094, 'HP:0000495', 'Recurrent corneal erosions', 'XPO:0101823', 'abnormal lens epithelium morphology', 0.4146341463414634, 9.014833150514745, 1.9333539892565992, 'UPHENO:0021038', 'abnormal anterior segment of eyeball morphology'),
(110095, 'HP:0000495', 'Recurrent corneal erosions', 'XPO:0125589', 'absent hyaloid blood vessel', 0.40789473684210525, 6.887869297006056, 1.6761639640277146, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(110096, 'HP:0000495', 'Recurrent corneal erosions', 'XPO:0130736', 'increased size of the cornea', 0.4470588235294118, 10.582693223545188, 2.1751060623084086, 'UPHENO:0020998', 'abnormal cornea morphology'),
(110097, 'HP:0000495', 'Recurrent corneal erosions', 'XPO:0102513', 'abnormal sclera morphology', 0.4246575342465753, 6.887869297006056, 1.7102589253909142, 'HP:0012372', 'Abnormal eye morphology'),
(110098, 'HP:0000495', 'Recurrent corneal erosions', 'XPO:0102550', 'abnormal lens morphology', 0.4657534246575342, 9.014833150514745, 2.0490703776514145, 'UPHENO:0021038', 'abnormal anterior segment of eyeball morphology'),
(110099, 'HP:0000495', 'Recurrent corneal erosions', 'XPO:0141638', 'neoplastic eye', 0.41333333333333333, 6.887869297006056, 1.6873013886368484, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(110100, 'HP:0000495', 'Recurrent corneal erosions', 'XPO:0128467', 'decreased size of the lens', 0.41975308641975306, 9.014833150514745, 1.9452516645636548, 'UPHENO:0021038', 'abnormal anterior segment of eyeball morphology'),
(110101, 'HP:0000495', 'Recurrent corneal erosions', 'XPO:0100371', 'abnormal hyaloid blood vessel', 0.484375, 6.887869297006056, 1.8265573330003382, 'HP:0012372', 'Abnormal eye morphology'),
(110102, 'HP:0000495', 'Recurrent corneal erosions', 'XPO:0140375', 'abnormally necrotic lens', 0.4358974358974359, 9.014833150514745, 1.982307406875276, 'UPHENO:0021038', 'abnormal anterior segment of eyeball morphology'),
(110103, 'HP:0000495', 'Recurrent corneal erosions', 'XPO:0129260', 'decreased size of the cornea', 0.4470588235294118, 10.582693223545188, 2.1751060623084086, 'UPHENO:0020998', 'abnormal cornea morphology'),
(110104, 'HP:0000495', 'Recurrent corneal erosions', 'XPO:0140473', 'abnormally necrotic lens transitional zone', 0.425, 9.014833150514745, 1.957371729889028, 'UPHENO:0021038', 'abnormal anterior segment of eyeball morphology'),
(110105, 'HP:0000495', 'Recurrent corneal erosions', 'XPO:0133371', 'eye fused with olfactory pit', 0.41333333333333333, 6.887869297006056, 1.6873013886368484, 'HP:0012372', 'Abnormal eye morphology'),
(110106, 'HP:0000495', 'Recurrent corneal erosions', 'XPO:0127645', 'abnormally localised hyaloid vein', 0.4025974025974026, 6.887869297006056, 1.6652442128423794, 'HP:0012372', 'Abnormal eye morphology'),
(110107, 'HP:0000495', 'Recurrent corneal erosions', 'XPO:0130893', 'increased size of the pupil', 0.40476190476190477, 9.014833150514745, 1.910199213986099, 'UPHENO:0021038', 'abnormal anterior segment of eyeball morphology'),
(110108, 'HP:0000495', 'Recurrent corneal erosions', 'XPO:0133369', 'eye fused with brain', 0.41333333333333333, 6.887869297006056, 1.6873013886368484, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(110109, 'HP:0000495', 'Recurrent corneal erosions', 'XPO:0141323', 'edematous eye', 0.4189189189189189, 6.887869297006056, 1.6986638159319787, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(110110, 'HP:0000495', 'Recurrent corneal erosions', 'XPO:0141343', 'decreased pigmentation in the eye', 0.41333333333333333, 6.887869297006056, 1.6873013886368484, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(110111, 'HP:0000495', 'Recurrent corneal erosions', 'XPO:0127230', 'abnormally localised hyaloid blood vessel', 0.4246575342465753, 6.887869297006056, 1.7102589253909142, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(110112, 'HP:0000495', 'Recurrent corneal erosions', 'XPO:0100710', 'abnormal hyaloid vein', 0.4696969696969697, 6.887869297006056, 1.7986693238259617, 'HP:0012372', 'Abnormal eye morphology'),
(110113, 'HP:0000495', 'Recurrent corneal erosions', 'XPO:0102805', 'abnormal retinal layer morphology', 0.4025974025974026, 6.887869297006056, 1.6652442128423794, 'HP:0012372', 'Abnormal eye morphology'),
(110114, 'HP:0000495', 'Recurrent corneal erosions', 'XPO:0129947', 'increased size of the lens', 0.41975308641975306, 9.014833150514745, 1.9452516645636548, 'UPHENO:0021038', 'abnormal anterior segment of eyeball morphology'),
(110115, 'HP:0000495', 'Recurrent corneal erosions', 'XPO:0141337', 'increased pigmentation in the eye', 0.41333333333333333, 6.887869297006056, 1.6873013886368484, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(110116, 'HP:0000495', 'Recurrent corneal erosions', 'XPO:0102003', 'abnormal hyaloid blood vessel morphology', 0.4025974025974026, 6.887869297006056, 1.6652442128423794, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(110117, 'HP:0000495', 'Recurrent corneal erosions', 'XPO:0140250', 'abnormally necrotic iris', 0.40476190476190477, 9.014833150514745, 1.910199213986099, 'UPHENO:0021038', 'abnormal anterior segment of eyeball morphology'),
(110118, 'HP:0000495', 'Recurrent corneal erosions', 'XPO:0102862', 'abnormal iris morphology', 0.43037974683544306, 9.014833150514745, 1.969721200851099, 'UPHENO:0021038', 'abnormal anterior segment of eyeball morphology'),
(110119, 'HP:0000495', 'Recurrent corneal erosions', 'XPO:0115423', 'abnormally incomplete structure of eye', 0.4246575342465753, 6.887869297006056, 1.7102589253909142, 'HP:0012372', 'Abnormal eye morphology'),
(110120, 'HP:0000495', 'Recurrent corneal erosions', 'XPO:0101817', 'abnormal eye morphology', 0.4305555555555556, 6.887869297006056, 1.7220947685207388, 'HP:0012372', 'Abnormal eye morphology'),
(110121, 'HP:0000495', 'Recurrent corneal erosions', 'XPO:0130285', 'increased size of the lens transitional zone', 0.4146341463414634, 9.014833150514745, 1.9333539892565992, 'UPHENO:0021038', 'abnormal anterior segment of eyeball morphology'),
(110122, 'HP:0000495', 'Recurrent corneal erosions', 'XPO:0133372', 'eye fused with olfactory epithelium', 0.41333333333333333, 6.887869297006056, 1.6873013886368484, 'HP:0012372', 'Abnormal eye morphology'),
(110123, 'HP:0000495', 'Recurrent corneal erosions', 'XPO:0128807', 'decreased size of the lens transitional zone', 0.4146341463414634, 9.014833150514745, 1.9333539892565992, 'UPHENO:0021038', 'abnormal anterior segment of eyeball morphology'),
(110124, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0130413', 'increased size of the central retina', 0.5308641975308642, 8.040873045973026, 2.066061861851679, 'HP:0000479', 'Abnormal retinal morphology'),
(110125, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0130001', 'increased size of the horizontal cell', 0.40186915887850466, 8.040873045973026, 1.797603651429875, 'HP:0000479', 'Abnormal retinal morphology'),
(110126, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0129981', 'increased size of the retinal ganglion cell layer', 0.4387755102040816, 8.040873045973026, 1.8783338822565765, 'HP:0000479', 'Abnormal retinal morphology'),
(110127, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0140192', 'abnormally necrotic retina', 0.5308641975308642, 8.040873045973026, 2.066061861851679, 'HP:0000479', 'Abnormal retinal morphology'),
(110128, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0102818', 'abnormal optic chiasm morphology', 0.4606741573033708, 7.796308075334707, 1.8951405363936156, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(110129, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0140240', 'abnormally necrotic eye photoreceptor cell', 0.44329896907216493, 8.040873045973026, 1.8879911895239345, 'HP:0000479', 'Abnormal retinal morphology'),
(110130, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0140538', 'abnormally necrotic optic disc', 0.4025974025974026, 6.575878401988876, 1.627092979653308, 'UPHENO:0087924', 'abnormal camera-type eye morphology'),
(110131, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0129911', 'increased size of the retinal inner nuclear layer', 0.4387755102040816, 8.040873045973026, 1.8783338822565765, 'HP:0000479', 'Abnormal retinal morphology'),
(110132, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0102196', 'abnormal central retina morphology', 0.5657894736842105, 8.040873045973026, 2.1329419421640696, 'HP:0000479', 'Abnormal retinal morphology'),
(110133, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0128295', 'decreased size of the retinal neural layer', 0.4387755102040816, 8.040873045973026, 1.8783338822565765, 'HP:0000479', 'Abnormal retinal morphology'),
(110134, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0129432', 'decreased size of the retinal stem cell', 0.4215686274509804, 8.040873045973026, 1.8411354685352277, 'HP:0000479', 'Abnormal retinal morphology'),
(110135, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0129741', 'increased size of the optic fiber layer', 0.4387755102040816, 8.040873045973026, 1.8783338822565765, 'HP:0000479', 'Abnormal retinal morphology'),
(110136, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0140620', 'abnormally necrotic horizontal cell', 0.43434343434343436, 8.040873045973026, 1.8688232698432123, 'HP:0000479', 'Abnormal retinal morphology'),
(110137, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0133371', 'eye fused with olfactory pit', 0.4375, 6.887869297006056, 1.7359270772241988, 'HP:0012372', 'Abnormal eye morphology'),
(110138, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0140218', 'abnormally necrotic sclera', 0.42168674698795183, 6.887869297006056, 1.7042661756699493, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(110139, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0141323', 'edematous eye', 0.4430379746835443, 6.887869297006056, 1.7468794071802813, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(110140, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0128475', 'decreased size of the retinal stem cell region', 0.5058823529411764, 8.040873045973026, 2.0168628550791743, 'HP:0000479', 'Abnormal retinal morphology'),
(110141, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0115423', 'abnormally incomplete structure of eye', 0.44871794871794873, 6.887869297006056, 1.7580416894914344, 'HP:0012372', 'Abnormal eye morphology'),
(110142, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0129810', 'increased size of the retinal progenitor cell region', 0.5058823529411764, 8.040873045973026, 2.0168628550791743, 'HP:0000479', 'Abnormal retinal morphology'),
(110143, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0129388', 'decreased size of the sclera', 0.4117647058823529, 6.887869297006056, 1.6840966347682629, 'HP:0012372', 'Abnormal eye morphology'),
(110144, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0102581', 'abnormal outer limiting membrane morphology', 0.4777777777777778, 8.040873045973026, 1.960038381077836, 'HP:0000479', 'Abnormal retinal morphology'),
(110145, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0130863', 'increased size of the sclera', 0.4117647058823529, 6.887869297006056, 1.6840966347682629, 'HP:0012372', 'Abnormal eye morphology'),
(110146, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0101961', 'abnormal retinal blood vessel morphology', 0.46236559139784944, 8.040873045973026, 1.9281657141584967, 'HP:0000479', 'Abnormal retinal morphology'),
(110147, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0140346', 'abnormally necrotic retinal blood vessel', 0.43, 8.040873045973026, 1.859455675666511, 'HP:0000479', 'Abnormal retinal morphology'),
(110148, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0140869', 'abnormally necrotic optic chiasm', 0.43617021276595747, 7.796308075334707, 1.844049172882245, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(110149, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0140797', 'abnormally necrotic bipolar neuron', 0.4174757281553398, 8.040873045973026, 1.8321761186829812, 'HP:0000479', 'Abnormal retinal morphology'),
(110150, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0141337', 'increased pigmentation in the eye', 0.4375, 6.887869297006056, 1.7359270772241988, 'HP:0012372', 'Abnormal eye morphology'),
(110151, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0130257', 'increased size of the retinal blood vessel', 0.4215686274509804, 8.040873045973026, 1.8411354685352277, 'HP:0000479', 'Abnormal retinal morphology'),
(110152, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0102441', 'abnormal retinal inner plexiform layer morphology', 0.4777777777777778, 8.040873045973026, 1.960038381077836, 'HP:0000479', 'Abnormal retinal morphology'),
(110153, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0102239', 'abnormal retinal pigmented epithelium morphology', 0.4777777777777778, 8.040873045973026, 1.960038381077836, 'HP:0000479', 'Abnormal retinal morphology'),
(110154, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0141343', 'decreased pigmentation in the eye', 0.4375, 6.887869297006056, 1.7359270772241988, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(110155, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0125909', 'absent retinal blood vessel', 0.4777777777777778, 8.040873045973026, 1.960038381077836, 'HP:0000479', 'Abnormal retinal morphology'),
(110156, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0129775', 'increased size of the retinal neural layer', 0.4387755102040816, 8.040873045973026, 1.8783338822565765, 'HP:0000479', 'Abnormal retinal morphology'),
(110157, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0103186', 'abnormal peripheral retina morphology', 0.5443037974683544, 8.040873045973026, 2.0920510830006163, 'HP:0000479', 'Abnormal retinal morphology'),
(110158, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0128884', 'decreased size of the retinal pigmented epithelium', 0.43434343434343436, 8.040873045973026, 1.8688232698432123, 'HP:0000479', 'Abnormal retinal morphology'),
(110159, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0141333', 'increased pigmentation in the retinal pigmented epithelium', 0.46236559139784944, 8.040873045973026, 1.9281657141584967, 'HP:0000479', 'Abnormal retinal morphology'),
(110160, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0140487', 'abnormally necrotic retinal layer', 0.5375, 8.040873045973026, 2.0789346459690603, 'HP:0000479', 'Abnormal retinal morphology'),
(110161, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0140391', 'abnormally necrotic central retina', 0.5443037974683544, 8.040873045973026, 2.0920510830006163, 'HP:0000479', 'Abnormal retinal morphology'),
(110162, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0130148', 'increased size of the ciliary marginal zone', 0.4574468085106383, 8.040873045973026, 1.9178820903589395, 'HP:0000479', 'Abnormal retinal morphology'),
(110163, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0102505', 'abnormal retinal stem cell region morphology', 0.5375, 8.040873045973026, 2.0789346459690603, 'HP:0000479', 'Abnormal retinal morphology'),
(110164, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0130265', 'increased size of the peripheral retina', 0.4942528735632184, 8.040873045973026, 1.9935457378573478, 'HP:0000479', 'Abnormal retinal morphology'),
(110165, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0140464', 'abnormally necrotic retinal pigmented epithelium', 0.4387755102040816, 8.040873045973026, 1.8783338822565765, 'HP:0000479', 'Abnormal retinal morphology'),
(110166, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0102162', 'abnormal ciliary marginal zone morphology', 0.5119047619047619, 8.040873045973026, 2.028832472656439, 'HP:0000479', 'Abnormal retinal morphology'),
(110167, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0102017', 'abnormal retinal neural layer morphology', 0.48314606741573035, 8.040873045973026, 1.9710190741722953, 'HP:0000479', 'Abnormal retinal morphology'),
(110168, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0128100', 'decreased size of the inner limiting membrane', 0.4387755102040816, 8.040873045973026, 1.8783338822565765, 'HP:0000479', 'Abnormal retinal morphology'),
(110169, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0102232', 'abnormal eye photoreceptor cell morphology', 0.46236559139784944, 8.040873045973026, 1.9281657141584967, 'HP:0000479', 'Abnormal retinal morphology'),
(110170, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0128521', 'decreased size of the horizontal cell', 0.40186915887850466, 8.040873045973026, 1.797603651429875, 'HP:0000479', 'Abnormal retinal morphology'),
(110171, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0102450', 'abnormal retinal stem cell morphology', 0.48314606741573035, 8.040873045973026, 1.9710190741722953, 'HP:0000479', 'Abnormal retinal morphology'),
(110172, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0102939', 'abnormal retinal ganglion cell layer morphology', 0.4777777777777778, 8.040873045973026, 1.960038381077836, 'HP:0000479', 'Abnormal retinal morphology'),
(110173, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0101359', 'abnormal hyaloid artery', 0.4117647058823529, 6.887869297006056, 1.6840966347682629, 'HP:0012372', 'Abnormal eye morphology'),
(110174, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0102946', 'abnormal retinal inner nuclear layer morphology', 0.4777777777777778, 8.040873045973026, 1.960038381077836, 'HP:0000479', 'Abnormal retinal morphology'),
(110175, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0140808', 'abnormally necrotic retinal cone cell', 0.43, 8.040873045973026, 1.859455675666511, 'HP:0000479', 'Abnormal retinal morphology'),
(110176, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0100329', 'abnormal retinal blood vessel', 0.5733333333333334, 8.040873045973026, 2.147114469784475, 'HP:0000479', 'Abnormal retinal morphology'),
(110177, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0101861', 'abnormal photoreceptor layer morphology', 0.48314606741573035, 8.040873045973026, 1.9710190741722953, 'HP:0000479', 'Abnormal retinal morphology'),
(110178, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0103184', 'abnormal inner limiting membrane morphology', 0.4777777777777778, 8.040873045973026, 1.960038381077836, 'HP:0000479', 'Abnormal retinal morphology'),
(110179, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0133369', 'eye fused with brain', 0.4375, 6.887869297006056, 1.7359270772241988, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(110180, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0100779', 'abnormal optic choroid vascular plexus', 0.4189189189189189, 6.887869297006056, 1.6986638159319787, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(110181, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0140317', 'abnormally necrotic retinal progenitor cell', 0.4574468085106383, 8.040873045973026, 1.9178820903589395, 'HP:0000479', 'Abnormal retinal morphology'),
(110182, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0130614', 'increased size of the retinal progenitor cell', 0.4215686274509804, 8.040873045973026, 1.8411354685352277, 'HP:0000479', 'Abnormal retinal morphology'),
(110183, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0102212', 'abnormal globe morphology', 0.40789473684210525, 6.575878401988876, 1.6377625561371638, 'UPHENO:0087924', 'abnormal camera-type eye morphology'),
(110184, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0130189', 'increased size of the optic chiasm', 0.41836734693877553, 7.796308075334707, 1.8060234564908433, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(110185, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0103155', 'abnormal bipolar neuron morphology', 0.44329896907216493, 8.040873045973026, 1.8879911895239345, 'HP:0000479', 'Abnormal retinal morphology'),
(110186, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0102831', 'abnormal optic disc morphology', 0.4189189189189189, 6.575878401988876, 1.6597469298370302, 'UPHENO:0087924', 'abnormal camera-type eye morphology'),
(110187, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0103210', 'abnormal pupil morphology', 0.40229885057471265, 6.887869297006056, 1.6646266551675757, 'HP:0012372', 'Abnormal eye morphology'),
(110188, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0103022', 'abnormal ciliary body morphology', 0.4117647058823529, 6.887869297006056, 1.6840966347682629, 'HP:0012372', 'Abnormal eye morphology'),
(110189, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0140945', 'abnormally necrotic retinal ganglion cell layer', 0.44329896907216493, 8.040873045973026, 1.8879911895239345, 'HP:0000479', 'Abnormal retinal morphology'),
(110190, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0103086', 'abnormal amacrine cell morphology', 0.44329896907216493, 8.040873045973026, 1.8879911895239345, 'HP:0000479', 'Abnormal retinal morphology'),
(110191, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0129029', 'decreased size of the Muller cell', 0.44329896907216493, 8.040873045973026, 1.8879911895239345, 'HP:0000479', 'Abnormal retinal morphology'),
(110192, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0130125', 'increased size of the outer limiting membrane', 0.4387755102040816, 8.040873045973026, 1.8783338822565765, 'HP:0000479', 'Abnormal retinal morphology'),
(110193, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0130515', 'increased size of the retinal outer nuclear layer', 0.4387755102040816, 8.040873045973026, 1.8783338822565765, 'HP:0000479', 'Abnormal retinal morphology'),
(110194, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0129371', 'decreased size of the retinal outer plexiform layer', 0.4387755102040816, 8.040873045973026, 1.8783338822565765, 'HP:0000479', 'Abnormal retinal morphology'),
(110195, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0133354', 'fused eyes', 0.4375, 6.887869297006056, 1.7359270772241988, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(110196, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0102963', 'abnormal retinal outer nuclear layer morphology', 0.4777777777777778, 8.040873045973026, 1.960038381077836, 'HP:0000479', 'Abnormal retinal morphology'),
(110197, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0129681', 'increased size of the eye photoreceptor cell', 0.4095238095238095, 8.040873045973026, 1.8146429295275122, 'HP:0000479', 'Abnormal retinal morphology'),
(110198, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0102476', 'abnormal lens transitional zone morphology', 0.42168674698795183, 6.887869297006056, 1.7042661756699493, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(110199, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0128710', 'decreased size of the optic chiasm', 0.41836734693877553, 7.796308075334707, 1.8060234564908433, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(110200, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0129955', 'increased size of the retinal stem cell region', 0.5058823529411764, 8.040873045973026, 2.0168628550791743, 'HP:0000479', 'Abnormal retinal morphology'),
(110201, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0140520', 'abnormally necrotic retinal outer nuclear layer', 0.44329896907216493, 8.040873045973026, 1.8879911895239345, 'HP:0000479', 'Abnormal retinal morphology'),
(110202, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0128201', 'decreased size of the eye photoreceptor cell', 0.4095238095238095, 8.040873045973026, 1.8146429295275122, 'HP:0000479', 'Abnormal retinal morphology'),
(110203, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0140081', 'abnormally necrotic amacrine cell', 0.4174757281553398, 8.040873045973026, 1.8321761186829812, 'HP:0000479', 'Abnormal retinal morphology'),
(110204, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0130761', 'increased size of the retinal inner plexiform layer', 0.4387755102040816, 8.040873045973026, 1.8783338822565765, 'HP:0000479', 'Abnormal retinal morphology'),
(110205, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0102550', 'abnormal lens morphology', 0.43209876543209874, 6.887869297006056, 1.7251781994025936, 'HP:0012372', 'Abnormal eye morphology'),
(110206, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0140375', 'abnormally necrotic lens', 0.4069767441860465, 6.887869297006056, 1.6742767456052652, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(110207, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0130122', 'increased size of the retinal layer', 0.5308641975308642, 8.040873045973026, 2.066061861851679, 'HP:0000479', 'Abnormal retinal morphology'),
(110208, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0140439', 'abnormally necrotic retinal stem cell', 0.4574468085106383, 8.040873045973026, 1.9178820903589395, 'HP:0000479', 'Abnormal retinal morphology'),
(110209, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0128431', 'decreased size of the retinal inner nuclear layer', 0.4387755102040816, 8.040873045973026, 1.8783338822565765, 'HP:0000479', 'Abnormal retinal morphology'),
(110210, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0141033', 'abnormally necrotic photoreceptor layer', 0.4479166666666667, 8.040873045973026, 1.8977990019604511, 'HP:0000479', 'Abnormal retinal morphology'),
(110211, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0102266', 'abnormal horizontal cell morphology', 0.4574468085106383, 8.040873045973026, 1.9178820903589395, 'HP:0000479', 'Abnormal retinal morphology'),
(110212, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0102756', 'abnormal Muller cell morphology', 0.5119047619047619, 8.040873045973026, 2.028832472656439, 'HP:0000479', 'Abnormal retinal morphology'),
(110213, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0130362', 'increased size of the retinal pigmented epithelium', 0.43434343434343436, 8.040873045973026, 1.8688232698432123, 'HP:0000479', 'Abnormal retinal morphology'),
(110214, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0141156', 'abnormally necrotic outer limiting membrane', 0.44329896907216493, 8.040873045973026, 1.8879911895239345, 'HP:0000479', 'Abnormal retinal morphology'),
(110215, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0102882', 'abnormal retinal cone cell morphology', 0.45263157894736844, 8.040873045973026, 1.9077612698957138, 'HP:0000479', 'Abnormal retinal morphology'),
(110216, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0102513', 'abnormal sclera morphology', 0.44871794871794873, 6.887869297006056, 1.7580416894914344, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(110217, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0101817', 'abnormal eye morphology', 0.45454545454545453, 6.887869297006056, 1.769420718895678, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(110218, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0102851', 'abnormal retinal rod cell morphology', 0.45263157894736844, 8.040873045973026, 1.9077612698957138, 'HP:0000479', 'Abnormal retinal morphology'),
(110219, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0129138', 'decreased size of the retinal progenitor cell', 0.4215686274509804, 8.040873045973026, 1.8411354685352277, 'HP:0000479', 'Abnormal retinal morphology'),
(110220, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0140271', 'abnormally necrotic peripheral retina', 0.5058823529411764, 8.040873045973026, 2.0168628550791743, 'HP:0000479', 'Abnormal retinal morphology'),
(110221, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0140553', 'abnormally necrotic retinal stem cell region', 0.5180722891566265, 8.040873045973026, 2.0410177622316423, 'HP:0000479', 'Abnormal retinal morphology'),
(110222, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0128646', 'decreased size of the outer limiting membrane', 0.4387755102040816, 8.040873045973026, 1.8783338822565765, 'HP:0000479', 'Abnormal retinal morphology'),
(110223, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0100710', 'abnormal hyaloid vein', 0.41333333333333333, 6.887869297006056, 1.6873013886368484, 'HP:0012372', 'Abnormal eye morphology'),
(110224, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0140489', 'abnormally necrotic ciliary marginal zone', 0.4673913043478261, 8.040873045973026, 1.938616553383523, 'HP:0000479', 'Abnormal retinal morphology'),
(110225, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0141638', 'neoplastic eye', 0.4375, 6.887869297006056, 1.7359270772241988, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(110226, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0128875', 'decreased size of the photoreceptor layer', 0.44329896907216493, 8.040873045973026, 1.8879911895239345, 'HP:0000479', 'Abnormal retinal morphology'),
(110227, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0139912', 'abnormally necrotic optic fiber layer', 0.44329896907216493, 8.040873045973026, 1.8879911895239345, 'HP:0000479', 'Abnormal retinal morphology'),
(110228, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0128935', 'decreased size of the central retina', 0.5308641975308642, 8.040873045973026, 2.066061861851679, 'HP:0000479', 'Abnormal retinal morphology'),
(110229, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0140491', 'abnormally necrotic retinal rod cell', 0.43, 8.040873045973026, 1.859455675666511, 'HP:0000479', 'Abnormal retinal morphology'),
(110230, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0141014', 'abnormally necrotic retinal outer plexiform layer', 0.44329896907216493, 8.040873045973026, 1.8879911895239345, 'HP:0000479', 'Abnormal retinal morphology'),
(110231, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0128643', 'decreased size of the retinal layer', 0.5308641975308642, 8.040873045973026, 2.066061861851679, 'HP:0000479', 'Abnormal retinal morphology'),
(110232, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0128300', 'decreased size of the retina', 0.5180722891566265, 8.040873045973026, 2.0410177622316423, 'HP:0000479', 'Abnormal retinal morphology'),
(110233, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0141182', 'abnormally necrotic inner limiting membrane', 0.44329896907216493, 8.040873045973026, 1.8879911895239345, 'HP:0000479', 'Abnormal retinal morphology'),
(110234, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0140531', 'abnormally necrotic retinal progenitor cell region', 0.5180722891566265, 8.040873045973026, 2.0410177622316423, 'HP:0000479', 'Abnormal retinal morphology'),
(110235, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0130506', 'increased size of the Muller cell', 0.44329896907216493, 8.040873045973026, 1.8879911895239345, 'HP:0000479', 'Abnormal retinal morphology'),
(110236, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0103926', 'decreased pigmentation in the retinal pigmented epithelium', 0.46236559139784944, 8.040873045973026, 1.9281657141584967, 'HP:0000479', 'Abnormal retinal morphology'),
(110237, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0128501', 'decreased size of the retinal ganglion cell layer', 0.4387755102040816, 8.040873045973026, 1.8783338822565765, 'HP:0000479', 'Abnormal retinal morphology'),
(110238, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0140006', 'abnormally necrotic retinal neural layer', 0.44329896907216493, 8.040873045973026, 1.8879911895239345, 'HP:0000479', 'Abnormal retinal morphology'),
(110239, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0128669', 'decreased size of the ciliary marginal zone', 0.4574468085106383, 8.040873045973026, 1.9178820903589395, 'HP:0000479', 'Abnormal retinal morphology'),
(110240, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0129780', 'increased size of the retina', 0.5180722891566265, 8.040873045973026, 2.0410177622316423, 'HP:0000479', 'Abnormal retinal morphology'),
(110241, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0140948', 'abnormally necrotic retinal inner nuclear layer', 0.44329896907216493, 8.040873045973026, 1.8879911895239345, 'HP:0000479', 'Abnormal retinal morphology'),
(110242, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0102663', 'abnormal retinal progenitor cell morphology', 0.48314606741573035, 8.040873045973026, 1.9710190741722953, 'HP:0000479', 'Abnormal retinal morphology'),
(110243, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0130845', 'increased size of the retinal outer plexiform layer', 0.4387755102040816, 8.040873045973026, 1.8783338822565765, 'HP:0000479', 'Abnormal retinal morphology'),
(110244, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0141138', 'abnormally necrotic retinal inner plexiform layer', 0.44329896907216493, 8.040873045973026, 1.8879911895239345, 'HP:0000479', 'Abnormal retinal morphology'),
(110245, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0133372', 'eye fused with olfactory epithelium', 0.4375, 6.887869297006056, 1.7359270772241988, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(110246, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0130906', 'increased size of the retinal stem cell', 0.4215686274509804, 8.040873045973026, 1.8411354685352277, 'HP:0000479', 'Abnormal retinal morphology'),
(110247, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0128779', 'decreased size of the retinal blood vessel', 0.4215686274509804, 8.040873045973026, 1.8411354685352277, 'HP:0000479', 'Abnormal retinal morphology'),
(110248, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0102117', 'abnormal retina morphology', 0.5657894736842105, 8.040873045973026, 2.1329419421640696, 'HP:0000479', 'Abnormal retinal morphology'),
(110249, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0102815', 'abnormal retinal ganglion cell morphology', 0.4479166666666667, 8.040873045973026, 1.8977990019604511, 'HP:0000479', 'Abnormal retinal morphology'),
(110250, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0139887', 'abnormally necrotic Muller cell', 0.48314606741573035, 8.040873045973026, 1.9710190741722953, 'HP:0000479', 'Abnormal retinal morphology'),
(110251, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0129038', 'decreased size of the retinal outer nuclear layer', 0.4387755102040816, 8.040873045973026, 1.8783338822565765, 'HP:0000479', 'Abnormal retinal morphology'),
(110252, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0128787', 'decreased size of the peripheral retina', 0.4942528735632184, 8.040873045973026, 1.9935457378573478, 'HP:0000479', 'Abnormal retinal morphology'),
(110253, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0100371', 'abnormal hyaloid blood vessel', 0.4246575342465753, 6.887869297006056, 1.7102589253909142, 'HP:0012372', 'Abnormal eye morphology'),
(110254, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0101315', 'abnormal hyaloid vascular plexus', 0.41333333333333333, 6.887869297006056, 1.6873013886368484, 'HP:0012372', 'Abnormal eye morphology'),
(110255, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0129580', 'increased size of the inner limiting membrane', 0.4387755102040816, 8.040873045973026, 1.8783338822565765, 'HP:0000479', 'Abnormal retinal morphology'),
(110256, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0103226', 'abnormal retinal outer plexiform layer morphology', 0.4777777777777778, 8.040873045973026, 1.960038381077836, 'HP:0000479', 'Abnormal retinal morphology'),
(110257, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0102805', 'abnormal retinal layer morphology', 0.581081081081081, 8.040873045973026, 2.1615733164502497, 'HP:0000479', 'Abnormal retinal morphology'),
(110258, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0102862', 'abnormal iris morphology', 0.40229885057471265, 6.887869297006056, 1.6646266551675757, 'HP:0012372', 'Abnormal eye morphology'),
(110259, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0140671', 'abnormally necrotic retinal ganglion cell', 0.42574257425742573, 8.040873045973026, 1.850227550835222, 'HP:0000479', 'Abnormal retinal morphology'),
(110260, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0139731', 'abnormally necrotic eye', 0.4166666666666667, 6.887869297006056, 1.6940913612964297, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(110261, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0102996', 'abnormal optic fiber layer morphology', 0.4777777777777778, 8.040873045973026, 1.960038381077836, 'HP:0000479', 'Abnormal retinal morphology'),
(110262, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0129285', 'decreased size of the retinal inner plexiform layer', 0.4387755102040816, 8.040873045973026, 1.8783338822565765, 'HP:0000479', 'Abnormal retinal morphology'),
(110263, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0102784', 'abnormal retinal progenitor cell region morphology', 0.5375, 8.040873045973026, 2.0789346459690603, 'HP:0000479', 'Abnormal retinal morphology'),
(110264, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0127563', 'abnormally localised retinal blood vessel', 0.5058823529411764, 8.040873045973026, 2.0168628550791743, 'HP:0000479', 'Abnormal retinal morphology'),
(110265, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0128261', 'decreased size of the optic fiber layer', 0.4387755102040816, 8.040873045973026, 1.8783338822565765, 'HP:0000479', 'Abnormal retinal morphology'),
(110266, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0115417', 'abnormally wholly ventralized eye', 0.4166666666666667, 6.887869297006056, 1.6940913612964297, 'HP:0012372', 'Abnormal eye morphology'),
(110267, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0103048', 'abnormal cornea morphology', 0.4117647058823529, 6.887869297006056, 1.6840966347682629, 'HP:0012372', 'Abnormal eye morphology'),
(110268, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0128330', 'decreased size of the retinal progenitor cell region', 0.5058823529411764, 8.040873045973026, 2.0168628550791743, 'HP:0000479', 'Abnormal retinal morphology'),
(110269, 'HP:0012778', 'Retinal astrocytic hamartoma', 'XPO:0130353', 'increased size of the photoreceptor layer', 0.44329896907216493, 8.040873045973026, 1.8879911895239345, 'HP:0000479', 'Abnormal retinal morphology'),
(110270, 'HP:0033266', 'Glomerular pseudocrescent', 'XPO:0129137', 'decreased size of the glomeral nexus', 0.42857142857142855, 9.653629130356133, 2.034027931788422, 'HP:0031263', 'Abnormal renal corpuscle morphology'),
(110271, 'HP:0033266', 'Glomerular pseudocrescent', 'XPO:0141107', 'abnormally necrotic glomerular epithelial cell', 0.4074074074074074, 9.653629130356133, 1.9831691849338062, 'HP:0031263', 'Abnormal renal corpuscle morphology'),
(110272, 'HP:0033266', 'Glomerular pseudocrescent', 'XPO:0130613', 'increased size of the glomeral nexus', 0.42857142857142855, 9.653629130356133, 2.034027931788422, 'HP:0031263', 'Abnormal renal corpuscle morphology'),
(110273, 'HP:0033266', 'Glomerular pseudocrescent', 'XPO:0140815', 'abnormally necrotic mesonephric mesenchyme', 0.4262295081967213, 7.603795021646889, 1.800267150315539, 'HP:0012210', 'Abnormal renal morphology'),
(110274, 'HP:0033266', 'Glomerular pseudocrescent', 'XPO:0129781', 'increased size of the glomus', 0.4342105263157895, 9.653629130356133, 2.0473659627798284, 'HP:0031263', 'Abnormal renal corpuscle morphology'),
(110275, 'HP:0033266', 'Glomerular pseudocrescent', 'XPO:0101717', 'abnormal mesonephric sinus morphology', 0.5531914893617021, 7.603795021646889, 2.0509399534910666, 'HP:0012210', 'Abnormal renal morphology'),
(110276, 'HP:0033266', 'Glomerular pseudocrescent', 'XPO:0102807', 'abnormal proximal tubule branch morphology', 0.4084507042253521, 8.69044940390107, 1.8840435714330452, 'UPHENO:0076756', 'abnormal nephron morphology'),
(110277, 'HP:0033266', 'Glomerular pseudocrescent', 'XPO:0128342', 'decreased size of the mesonephric mesenchyme', 0.4126984126984127, 7.603795021646889, 1.7714610173294143, 'HP:0012210', 'Abnormal renal morphology'),
(110278, 'HP:0033266', 'Glomerular pseudocrescent', 'XPO:0128038', 'decreased size of the pronephric nephron', 0.4084507042253521, 8.69044940390107, 1.8840435714330452, 'UPHENO:0076756', 'abnormal nephron morphology'),
(110279, 'HP:0033266', 'Glomerular pseudocrescent', 'XPO:0129279', 'decreased size of the glomerulus', 0.4647887323943662, 9.653629130356133, 2.1182299323972256, 'HP:0031263', 'Abnormal renal corpuscle morphology'),
(110280, 'HP:0033266', 'Glomerular pseudocrescent', 'XPO:0129518', 'increased size of the pronephric nephron', 0.4084507042253521, 8.69044940390107, 1.8840435714330452, 'UPHENO:0076756', 'abnormal nephron morphology'),
(110281, 'HP:0033266', 'Glomerular pseudocrescent', 'XPO:0102198', 'abnormal kidney morphology', 0.48148148148148145, 7.603795021646889, 1.9133965851082877, 'HP:0012210', 'Abnormal renal morphology'),
(110282, 'HP:0033266', 'Glomerular pseudocrescent', 'XPO:0103121', 'abnormal mesonephric late proximal tubule morphology', 0.4264705882352941, 8.69044940390107, 1.9251548169720663, 'UPHENO:0076756', 'abnormal nephron morphology'),
(110283, 'HP:0033266', 'Glomerular pseudocrescent', 'XPO:0102467', 'abnormal pronephric tubule morphology', 0.4084507042253521, 8.69044940390107, 1.8840435714330452, 'UPHENO:0076756', 'abnormal nephron morphology'),
(110284, 'HP:0033266', 'Glomerular pseudocrescent', 'XPO:0101701', 'abnormal urinary system morphology', 0.425531914893617, 7.340144605965611, 1.7673329595106295, 'UPHENO:0087427', 'abnormal renal system morphology'),
(110285, 'HP:0033266', 'Glomerular pseudocrescent', 'XPO:0140525', 'abnormally necrotic pronephric nephron', 0.4142857142857143, 8.69044940390107, 1.897453303446231, 'UPHENO:0076756', 'abnormal nephron morphology'),
(110286, 'HP:0033266', 'Glomerular pseudocrescent', 'XPO:0102837', 'abnormal glomerular epithelial cell morphology', 0.4342105263157895, 9.653629130356133, 2.0473659627798284, 'HP:0031263', 'Abnormal renal corpuscle morphology'),
(110287, 'HP:0033266', 'Glomerular pseudocrescent', 'XPO:0107387', 'abnormal embryonic kidney morphology', 0.4642857142857143, 7.603795021646889, 1.8789181469418736, 'HP:0012210', 'Abnormal renal morphology'),
(110288, 'HP:0033266', 'Glomerular pseudocrescent', 'XPO:0130755', 'increased size of the glomerulus', 0.4520547945205479, 9.653629130356133, 2.089011568398011, 'HP:0031263', 'Abnormal renal corpuscle morphology'),
(110289, 'HP:0033266', 'Glomerular pseudocrescent', 'XPO:0101779', 'abnormal mesonephric mesenchyme morphology', 0.4727272727272727, 7.603795021646889, 1.8959222776686673, 'HP:0012210', 'Abnormal renal morphology'),
(110290, 'HP:0033266', 'Glomerular pseudocrescent', 'XPO:0102410', 'abnormal mesonephric kidney morphology', 0.4126984126984127, 7.603795021646889, 1.7714610173294143, 'HP:0012210', 'Abnormal renal morphology'),
(110291, 'HP:0033266', 'Glomerular pseudocrescent', 'XPO:0102582', 'abnormal pronephric nephron morphology', 0.453125, 8.69044940390107, 1.9844041640106163, 'UPHENO:0076756', 'abnormal nephron morphology'),
(110292, 'HP:0033266', 'Glomerular pseudocrescent', 'XPO:0102040', 'abnormal glomus morphology', 0.4925373134328358, 9.653629130356133, 2.180544096491188, 'HP:0031263', 'Abnormal renal corpuscle morphology'),
(110293, 'HP:0033266', 'Glomerular pseudocrescent', 'XPO:0129639', 'increased size of the mesonephric nephron', 0.43283582089552236, 8.69044940390107, 1.9394684327641227, 'UPHENO:0076756', 'abnormal nephron morphology'),
(110294, 'HP:0033266', 'Glomerular pseudocrescent', 'XPO:0128159', 'decreased size of the mesonephric nephron', 0.43283582089552236, 8.69044940390107, 1.9394684327641227, 'UPHENO:0076756', 'abnormal nephron morphology'),
(110295, 'HP:0033266', 'Glomerular pseudocrescent', 'XPO:0102743', 'abnormal mesonephric late distal tubule morphology', 0.4264705882352941, 8.69044940390107, 1.9251548169720663, 'UPHENO:0076756', 'abnormal nephron morphology'),
(110296, 'HP:0033266', 'Glomerular pseudocrescent', 'XPO:0103197', 'abnormal mesonephric early distal tubule morphology', 0.4264705882352941, 8.69044940390107, 1.9251548169720663, 'UPHENO:0076756', 'abnormal nephron morphology'),
(110297, 'HP:0033266', 'Glomerular pseudocrescent', 'XPO:0102909', 'abnormal glomerulus morphology', 0.515625, 9.653629130356133, 2.231065333050532, 'HP:0031263', 'Abnormal renal corpuscle morphology'),
(110298, 'HP:0033266', 'Glomerular pseudocrescent', 'XPO:0100147', 'abnormal mesonephric mesenchyme', 0.40425531914893614, 6.880013295263146, 1.6677175931270638, 'HP:0000077', 'Abnormality of the kidney'),
(110299, 'HP:0033266', 'Glomerular pseudocrescent', 'XPO:0130678', 'increased size of the mesonephric sinus', 0.5, 7.603795021646889, 1.9498455094759288, 'HP:0012210', 'Abnormal renal morphology'),
(110300, 'HP:0033266', 'Glomerular pseudocrescent', 'XPO:0103049', 'abnormal podocyte morphology', 0.4583333333333333, 9.653629130356133, 2.103468568360339, 'HP:0031263', 'Abnormal renal corpuscle morphology'),
(110301, 'HP:0033266', 'Glomerular pseudocrescent', 'XPO:0100085', 'abnormal mesonephric sinus', 0.4318181818181818, 6.880013295263146, 1.7236341932224046, 'HP:0000077', 'Abnormality of the kidney'),
(110302, 'HP:0033266', 'Glomerular pseudocrescent', 'XPO:0140802', 'abnormally necrotic glomerular mesangial cell', 0.4177215189873418, 9.653629130356133, 2.0081156899125148, 'HP:0031263', 'Abnormal renal corpuscle morphology'),
(110303, 'HP:0033266', 'Glomerular pseudocrescent', 'XPO:0101903', 'abnormal mesonephric nephron morphology', 0.48333333333333334, 8.69044940390107, 2.049483807828738, 'UPHENO:0076756', 'abnormal nephron morphology'),
(110304, 'HP:0033266', 'Glomerular pseudocrescent', 'XPO:0102199', 'abnormal mesonephric collecting duct morphology', 0.4027777777777778, 8.69044940390107, 1.8709141879823046, 'UPHENO:0076756', 'abnormal nephron morphology'),
(110305, 'HP:0033266', 'Glomerular pseudocrescent', 'XPO:0139856', 'abnormally necrotic glomeral nexus', 0.4342105263157895, 9.653629130356133, 2.0473659627798284, 'HP:0031263', 'Abnormal renal corpuscle morphology'),
(110306, 'HP:0033266', 'Glomerular pseudocrescent', 'XPO:0128301', 'decreased size of the glomus', 0.44594594594594594, 9.653629130356133, 2.0748486148025367, 'HP:0031263', 'Abnormal renal corpuscle morphology'),
(110307, 'HP:0033266', 'Glomerular pseudocrescent', 'XPO:0103182', 'abnormal pronephric sinus morphology', 0.41935483870967744, 7.603795021646889, 1.7856898484575028, 'HP:0012210', 'Abnormal renal morphology'),
(110308, 'HP:0033266', 'Glomerular pseudocrescent', 'XPO:0101902', 'abnormal mesonephric tubule morphology', 0.4393939393939394, 8.69044940390107, 1.9541061380293046, 'UPHENO:0076756', 'abnormal nephron morphology'),
(110309, 'HP:0033266', 'Glomerular pseudocrescent', 'XPO:0139909', 'abnormally necrotic mesonephric nephron', 0.4393939393939394, 8.69044940390107, 1.9541061380293046, 'UPHENO:0076756', 'abnormal nephron morphology'),
(110310, 'HP:0033266', 'Glomerular pseudocrescent', 'XPO:0103061', 'abnormal glomerular mesangial cell morphology', 0.44594594594594594, 9.653629130356133, 2.0748486148025367, 'HP:0031263', 'Abnormal renal corpuscle morphology'),
(110311, 'HP:0033266', 'Glomerular pseudocrescent', 'XPO:0140127', 'abnormally necrotic podocyte', 0.4342105263157895, 9.653629130356133, 2.0473659627798284, 'HP:0031263', 'Abnormal renal corpuscle morphology'),
(110312, 'HP:0033266', 'Glomerular pseudocrescent', 'XPO:0102585', 'abnormal mesonephric duct morphology', 0.4027777777777778, 8.69044940390107, 1.8709141879823046, 'UPHENO:0076756', 'abnormal nephron morphology'),
(110313, 'HP:0033266', 'Glomerular pseudocrescent', 'XPO:0102393', 'abnormal ureter morphology', 0.4074074074074074, 7.340144605965611, 1.7292857727720756, 'UPHENO:0087427', 'abnormal renal system morphology'),
(110314, 'HP:0033266', 'Glomerular pseudocrescent', 'XPO:0102879', 'abnormal mesonephric early proximal tubule morphology', 0.4264705882352941, 8.69044940390107, 1.9251548169720663, 'UPHENO:0076756', 'abnormal nephron morphology'),
(110315, 'HP:0033266', 'Glomerular pseudocrescent', 'XPO:0129822', 'increased size of the mesonephric mesenchyme', 0.4126984126984127, 7.603795021646889, 1.7714610173294143, 'HP:0012210', 'Abnormal renal morphology'),
(110316, 'HP:0033266', 'Glomerular pseudocrescent', 'XPO:0107388', 'abnormal adult kidney morphology', 0.4642857142857143, 7.603795021646889, 1.8789181469418736, 'HP:0012210', 'Abnormal renal morphology'),
(110317, 'HP:0033266', 'Glomerular pseudocrescent', 'XPO:0102647', 'abnormal proximal tubule morphology', 0.4027777777777778, 8.69044940390107, 1.8709141879823046, 'UPHENO:0076756', 'abnormal nephron morphology'),
(110318, 'HP:0033266', 'Glomerular pseudocrescent', 'XPO:0140478', 'abnormally necrotic glomerulus', 0.4782608695652174, 9.653629130356133, 2.1487096272749926, 'HP:0031263', 'Abnormal renal corpuscle morphology'),
(110319, 'HP:0033266', 'Glomerular pseudocrescent', 'XPO:0102119', 'abnormal distal tubule morphology', 0.4027777777777778, 8.69044940390107, 1.8709141879823046, 'UPHENO:0076756', 'abnormal nephron morphology'),
(110320, 'HP:0033266', 'Glomerular pseudocrescent', 'XPO:0102671', 'abnormal glomeral nexus morphology', 0.4714285714285714, 9.653629130356133, 2.1333064922849307, 'HP:0031263', 'Abnormal renal corpuscle morphology'),
(110321, 'HP:0033266', 'Glomerular pseudocrescent', 'XPO:0129202', 'decreased size of the mesonephric sinus', 0.5, 7.603795021646889, 1.9498455094759288, 'HP:0012210', 'Abnormal renal morphology'),
(110322, 'HP:0033266', 'Glomerular pseudocrescent', 'XPO:0141643', 'neoplastic kidney', 0.45614035087719296, 7.603795021646889, 1.8623634793380868, 'HP:0012210', 'Abnormal renal morphology'),
(110323, 'HP:0033266', 'Glomerular pseudocrescent', 'XPO:0140005', 'abnormally necrotic glomus', 0.4583333333333333, 9.653629130356133, 2.103468568360339, 'HP:0031263', 'Abnormal renal corpuscle morphology'),
(110324, 'HP:0033266', 'Glomerular pseudocrescent', 'XPO:0140552', 'abnormally necrotic kidney', 0.41935483870967744, 7.603795021646889, 1.7856898484575028, 'HP:0012210', 'Abnormal renal morphology'),
(110325, 'HP:0025527', 'Serpiginous cutaneous lesion', 'XPO:0100533', 'abnormal melanoblast', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(110326, 'HP:0025527', 'Serpiginous cutaneous lesion', 'XPO:0100691', 'abnormal keratin accumulating cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(110327, 'HP:0025527', 'Serpiginous cutaneous lesion', 'XPO:0100653', 'abnormal myoblast', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(110328, 'HP:0025527', 'Serpiginous cutaneous lesion', 'XPO:0101237', 'abnormal mucus secreting cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(110329, 'HP:0025527', 'Serpiginous cutaneous lesion', 'XPO:0100791', 'abnormal multiciliated cell precursor', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(110330, 'HP:0025527', 'Serpiginous cutaneous lesion', 'XPO:0101254', 'abnormal stratum compactum', 0.4411764705882353, 6.8660902472206855, 1.740447489012273, 'HP:0000951', 'Abnormality of the skin'),
(110331, 'HP:0025527', 'Serpiginous cutaneous lesion', 'XPO:0102176', 'abnormal neuromast support cell morphology', 0.42857142857142855, 7.420886955069779, 1.7833620281931915, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(110332, 'HP:0025527', 'Serpiginous cutaneous lesion', 'XPO:0101297', 'abnormal barrier cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(110333, 'HP:0025527', 'Serpiginous cutaneous lesion', 'XPO:0100544', 'abnormal neuromast support cell', 0.4411764705882353, 6.8660902472206855, 1.740447489012273, 'HP:0000951', 'Abnormality of the skin'),
(110334, 'HP:0025527', 'Serpiginous cutaneous lesion', 'XPO:0100481', 'abnormal anatomical line', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(110335, 'HP:0025527', 'Serpiginous cutaneous lesion', 'XPO:0100507', 'abnormal skin', 0.5, 6.8660902472206855, 1.8528478414619864, 'HP:0000951', 'Abnormality of the skin'),
(110336, 'HP:0025527', 'Serpiginous cutaneous lesion', 'XPO:0101529', 'abnormal skin mucous gland', 0.4411764705882353, 6.8660902472206855, 1.740447489012273, 'HP:0000951', 'Abnormality of the skin'),
(110337, 'HP:0025527', 'Serpiginous cutaneous lesion', 'XPO:0100549', 'abnormal mitotic cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(110338, 'HP:0025527', 'Serpiginous cutaneous lesion', 'XPO:0102139', 'abnormal skin morphology', 0.46153846153846156, 7.420886955069779, 1.8506822386605823, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(110339, 'HP:0025527', 'Serpiginous cutaneous lesion', 'XPO:0101467', 'abnormal alkali secreting cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(110340, 'HP:0025527', 'Serpiginous cutaneous lesion', 'XPO:0100285', 'abnormal progenitor cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(110341, 'HP:0025527', 'Serpiginous cutaneous lesion', 'XPO:0102840', 'abnormal stratum spongiosum morphology', 0.42857142857142855, 7.420886955069779, 1.7833620281931915, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(110342, 'HP:0025527', 'Serpiginous cutaneous lesion', 'XPO:0101448', 'abnormal myelin accumulating cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(110343, 'HP:0025527', 'Serpiginous cutaneous lesion', 'XPO:0100704', 'abnormal Merkel cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(110344, 'HP:0025527', 'Serpiginous cutaneous lesion', 'XPO:0101014', 'abnormal goblet cell', 0.40540540540540543, 6.8660902472206855, 1.6683974647021622, 'HP:0000951', 'Abnormality of the skin'),
(110345, 'HP:0025527', 'Serpiginous cutaneous lesion', 'XPO:0101004', 'abnormal acid secreting cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(110346, 'HP:0025527', 'Serpiginous cutaneous lesion', 'XPO:0103147', 'abnormal neuromast mantle cell morphology', 0.42857142857142855, 7.420886955069779, 1.7833620281931915, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(110347, 'HP:0025527', 'Serpiginous cutaneous lesion', 'XPO:0100983', 'abnormal skin gland', 0.4838709677419355, 6.8660902472206855, 1.8227182263109507, 'HP:0000951', 'Abnormality of the skin'),
(110348, 'HP:0025527', 'Serpiginous cutaneous lesion', 'XPO:0100108', 'abnormal cell part', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(110349, 'HP:0025527', 'Serpiginous cutaneous lesion', 'XPO:0102626', 'abnormal granular gland morphology', 0.43902439024390244, 7.420886955069779, 1.8049793268950312, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(110350, 'HP:0025527', 'Serpiginous cutaneous lesion', 'XPO:0102886', 'abnormal stratum compactum morphology', 0.42857142857142855, 7.420886955069779, 1.7833620281931915, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(110351, 'HP:0025527', 'Serpiginous cutaneous lesion', 'XPO:0101095', 'abnormal skin seromucous gland', 0.46875, 6.8660902472206855, 1.7940122082596586, 'HP:0000951', 'Abnormality of the skin'),
(110352, 'HP:0025527', 'Serpiginous cutaneous lesion', 'XPO:0101278', 'abnormal pigment cell', 0.4411764705882353, 6.8660902472206855, 1.740447489012273, 'HP:0000951', 'Abnormality of the skin'),
(110353, 'HP:0025527', 'Serpiginous cutaneous lesion', 'XPO:0100802', 'abnormal exocrine cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(110354, 'HP:0025527', 'Serpiginous cutaneous lesion', 'XPO:0102561', 'abnormal dermis morphology', 0.45, 7.420886955069779, 1.8274022900777487, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(110355, 'HP:0025527', 'Serpiginous cutaneous lesion', 'XPO:0100477', 'abnormal pericyte', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(110356, 'HP:0025527', 'Serpiginous cutaneous lesion', 'XPO:0100289', 'abnormal chondroblast', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(110357, 'HP:0025527', 'Serpiginous cutaneous lesion', 'XPO:0103019', 'abnormal melanophore morphology', 0.4090909090909091, 7.420886955069779, 1.7423597190908553, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(110358, 'HP:0025527', 'Serpiginous cutaneous lesion', 'XPO:0102910', 'abnormal pigment cell morphology', 0.42857142857142855, 7.420886955069779, 1.7833620281931915, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(110359, 'HP:0025527', 'Serpiginous cutaneous lesion', 'XPO:0100026', 'abnormal germ cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(110360, 'HP:0025527', 'Serpiginous cutaneous lesion', 'XPO:0101326', 'abnormal cementoblast', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(110361, 'HP:0025527', 'Serpiginous cutaneous lesion', 'XPO:0101241', 'abnormal nucleate erythrocyte', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(110362, 'HP:0025527', 'Serpiginous cutaneous lesion', 'XPO:0101322', 'abnormal iridophore', 0.42857142857142855, 6.8660902472206855, 1.7154037734456928, 'HP:0000951', 'Abnormality of the skin'),
(110363, 'HP:0025527', 'Serpiginous cutaneous lesion', 'XPO:0100852', 'abnormal interdigital region', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(110364, 'HP:0025527', 'Serpiginous cutaneous lesion', 'XPO:0100715', 'abnormal ciliated cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(110365, 'HP:0025527', 'Serpiginous cutaneous lesion', 'XPO:0100004', 'abnormal cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(110366, 'HP:0025527', 'Serpiginous cutaneous lesion', 'XPO:0101208', 'abnormal stratum spongiosum', 0.4411764705882353, 6.8660902472206855, 1.740447489012273, 'HP:0000951', 'Abnormality of the skin'),
(110367, 'HP:0025527', 'Serpiginous cutaneous lesion', 'XPO:0100337', 'abnormal zygote', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(110368, 'HP:0025527', 'Serpiginous cutaneous lesion', 'XPO:0100638', 'abnormal polar body', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(110369, 'HP:0025527', 'Serpiginous cutaneous lesion', 'XPO:0101132', 'abnormal apoptotic cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(110370, 'HP:0025527', 'Serpiginous cutaneous lesion', 'XPO:0100929', 'abnormal dermis', 0.46875, 6.8660902472206855, 1.7940122082596586, 'HP:0000951', 'Abnormality of the skin'),
(110371, 'HP:0025527', 'Serpiginous cutaneous lesion', 'XPO:0101373', 'abnormal oxygen accumulating cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(110372, 'HP:0025527', 'Serpiginous cutaneous lesion', 'XPO:0102945', 'abnormal Eberth-Kastschenko layer morphology', 0.42857142857142855, 7.420886955069779, 1.7833620281931915, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(110373, 'HP:0025527', 'Serpiginous cutaneous lesion', 'XPO:0100172', 'abnormal stem cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(110374, 'HP:0025527', 'Serpiginous cutaneous lesion', 'XPO:0100994', 'abnormal granular gland', 0.46875, 6.8660902472206855, 1.7940122082596586, 'HP:0000951', 'Abnormality of the skin'),
(110375, 'HP:0025527', 'Serpiginous cutaneous lesion', 'XPO:0102727', 'abnormal skin seromucous gland morphology', 0.43902439024390244, 7.420886955069779, 1.8049793268950312, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(110376, 'HP:0025527', 'Serpiginous cutaneous lesion', 'XPO:0101333', 'abnormal barrier epithelial cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(110377, 'HP:0025527', 'Serpiginous cutaneous lesion', 'XPO:0100006', 'abnormal anatomical structure', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(110378, 'HP:0025527', 'Serpiginous cutaneous lesion', 'XPO:0100754', 'abnormal electrically active cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(110379, 'HP:0025527', 'Serpiginous cutaneous lesion', 'XPO:0101435', 'abnormal paracrine cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(110380, 'HP:0025527', 'Serpiginous cutaneous lesion', 'XPO:0101387', 'abnormal melanophore', 0.42857142857142855, 6.8660902472206855, 1.7154037734456928, 'HP:0000951', 'Abnormality of the skin'),
(110381, 'HP:0025527', 'Serpiginous cutaneous lesion', 'XPO:0103223', 'abnormal xanthophore morphology', 0.4090909090909091, 7.420886955069779, 1.7423597190908553, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(110382, 'HP:0025527', 'Serpiginous cutaneous lesion', 'XPO:0100344', 'abnormal portion of organism substance', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(110383, 'HP:0025527', 'Serpiginous cutaneous lesion', 'XPO:0102954', 'abnormal iridophore morphology', 0.4090909090909091, 7.420886955069779, 1.7423597190908553, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(110384, 'HP:0025527', 'Serpiginous cutaneous lesion', 'XPO:0101535', 'abnormal absorptive cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(110385, 'HP:0025527', 'Serpiginous cutaneous lesion', 'XPO:0100081', 'abnormal anatomical entity in vitro', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(110386, 'HP:0025527', 'Serpiginous cutaneous lesion', 'XPO:0101313', 'abnormal Eberth-Kastschenko layer', 0.4411764705882353, 6.8660902472206855, 1.740447489012273, 'HP:0000951', 'Abnormality of the skin'),
(110387, 'HP:0025527', 'Serpiginous cutaneous lesion', 'XPO:0102615', 'abnormal skin gland morphology', 0.46153846153846156, 7.420886955069779, 1.8506822386605823, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(110388, 'HP:0025527', 'Serpiginous cutaneous lesion', 'XPO:0101515', 'abnormal neuromast mantle cell', 0.4411764705882353, 6.8660902472206855, 1.740447489012273, 'HP:0000951', 'Abnormality of the skin'),
(110389, 'HP:0025527', 'Serpiginous cutaneous lesion', 'XPO:0101591', 'abnormal xanthophore', 0.42857142857142855, 6.8660902472206855, 1.7154037734456928, 'HP:0000951', 'Abnormality of the skin'),
(110390, 'HP:0001607', 'Subglottic stenosis', 'XPO:0129899', 'increased size of the pharynx', 0.4126984126984127, 7.783689670920507, 1.7922936065628097, 'HP:0002087', 'Abnormality of the upper respiratory tract'),
(110391, 'HP:0001607', 'Subglottic stenosis', 'XPO:0125599', 'absent pharyngeal epithelium', 0.4262295081967213, 7.783689670920507, 1.821438503049814, 'HP:0002087', 'Abnormality of the upper respiratory tract'),
(110392, 'HP:0001607', 'Subglottic stenosis', 'XPO:0141644', 'neoplastic larynx', 0.5882352941176471, 11.404694921567193, 2.590105030980426, 'HP:0025423', 'Abnormal larynx morphology'),
(110393, 'HP:0001607', 'Subglottic stenosis', 'XPO:0101474', 'abnormal aortic arch 5', 0.43333333333333335, 7.783689670920507, 1.8365544344593274, 'HP:0002087', 'Abnormality of the upper respiratory tract'),
(110394, 'HP:0001607', 'Subglottic stenosis', 'XPO:0141178', 'abnormally necrotic larynx', 0.5454545454545454, 11.404694921567193, 2.4941416728989547, 'HP:0025423', 'Abnormal larynx morphology'),
(110395, 'HP:0001607', 'Subglottic stenosis', 'XPO:0102668', 'abnormal pharynx morphology', 0.4642857142857143, 7.783689670920507, 1.9010144446167851, 'HP:0002087', 'Abnormality of the upper respiratory tract'),
(110396, 'HP:0001607', 'Subglottic stenosis', 'XPO:0102961', 'abnormal pharyngeal epithelium morphology', 0.41935483870967744, 7.783689670920507, 1.80668977041302, 'HP:0002087', 'Abnormality of the upper respiratory tract'),
(110397, 'HP:0001607', 'Subglottic stenosis', 'XPO:0101036', 'abnormal pharynx', 0.5416666666666666, 7.783689670920507, 2.053330279914869, 'HP:0002087', 'Abnormality of the upper respiratory tract'),
(110398, 'HP:0001607', 'Subglottic stenosis', 'XPO:0125326', 'absent oropharynx', 0.4262295081967213, 7.783689670920507, 1.821438503049814, 'HP:0002087', 'Abnormality of the upper respiratory tract'),
(110399, 'HP:0001607', 'Subglottic stenosis', 'XPO:0100804', 'abnormal larynx', 0.6666666666666666, 11.09310877090129, 2.719449548579184, 'UPHENO:0003032', 'abnormal larynx'),
(110400, 'HP:0001607', 'Subglottic stenosis', 'XPO:0101210', 'abnormal aortic arch 2', 0.43333333333333335, 7.783689670920507, 1.8365544344593274, 'HP:0002087', 'Abnormality of the upper respiratory tract'),
(110401, 'HP:0001607', 'Subglottic stenosis', 'XPO:0100360', 'abnormal aortic arch 6', 0.43333333333333335, 7.783689670920507, 1.8365544344593274, 'HP:0002087', 'Abnormality of the upper respiratory tract'),
(110402, 'HP:0001607', 'Subglottic stenosis', 'XPO:0139850', 'abnormally necrotic respiratory system', 0.5217391304347826, 7.241224942262181, 1.9437156182576012, 'HP:0012252', 'Abnormal respiratory system morphology'),
(110403, 'HP:0001607', 'Subglottic stenosis', 'XPO:0127859', 'abnormally localised larynx', 0.5384615384615384, 11.09310877090129, 2.4440156331539074, 'UPHENO:0003032', 'abnormal larynx'),
(110404, 'HP:0001607', 'Subglottic stenosis', 'XPO:0100875', 'abnormal oropharynx', 0.5098039215686274, 7.783689670920507, 1.9920229713807251, 'HP:0002087', 'Abnormality of the upper respiratory tract'),
(110405, 'HP:0001607', 'Subglottic stenosis', 'XPO:0128535', 'decreased size of the respiratory system', 0.5, 7.241224942262181, 1.9027907060764961, 'HP:0012252', 'Abnormal respiratory system morphology'),
(110406, 'HP:0001607', 'Subglottic stenosis', 'XPO:0101329', 'abnormal pharyngeal epithelium', 0.5306122448979592, 7.783689670920507, 2.032269925446959, 'HP:0002087', 'Abnormality of the upper respiratory tract'),
(110407, 'HP:0001607', 'Subglottic stenosis', 'XPO:0100716', 'abnormal aortic arch 3', 0.43333333333333335, 7.783689670920507, 1.8365544344593274, 'HP:0002087', 'Abnormality of the upper respiratory tract'),
(110408, 'HP:0001607', 'Subglottic stenosis', 'XPO:0101548', 'abnormal pulmonary vein', 0.4067796610169492, 7.241224942262181, 1.7162700916117157, 'HP:0012252', 'Abnormal respiratory system morphology'),
(110409, 'HP:0001607', 'Subglottic stenosis', 'XPO:0141614', 'metaplastic larynx', 0.6222222222222222, 11.09310877090129, 2.6272378633810503, 'UPHENO:0003032', 'abnormal larynx'),
(110410, 'HP:0001607', 'Subglottic stenosis', 'XPO:0126197', 'absent larynx', 0.5283018867924528, 11.09310877090129, 2.4208490853543636, 'UPHENO:0003032', 'abnormal larynx'),
(110411, 'HP:0001607', 'Subglottic stenosis', 'XPO:0126955', 'abnormally localised oropharynx', 0.4406779661016949, 7.783689670920507, 1.8520530588911377, 'HP:0002087', 'Abnormality of the upper respiratory tract'),
(110412, 'HP:0001607', 'Subglottic stenosis', 'XPO:0140110', 'abnormally necrotic pharynx', 0.4262295081967213, 7.783689670920507, 1.821438503049814, 'HP:0002087', 'Abnormality of the upper respiratory tract'),
(110413, 'HP:0001607', 'Subglottic stenosis', 'XPO:0129144', 'decreased size of the larynx', 0.5263157894736842, 11.404694921567193, 2.449994083942072, 'HP:0025423', 'Abnormal larynx morphology'),
(110414, 'HP:0001607', 'Subglottic stenosis', 'XPO:0130620', 'increased size of the larynx', 0.5263157894736842, 11.404694921567193, 2.449994083942072, 'HP:0025423', 'Abnormal larynx morphology'),
(110415, 'HP:0001607', 'Subglottic stenosis', 'XPO:0128419', 'decreased size of the pharynx', 0.40625, 7.783689670920507, 1.778236184766089, 'HP:0002087', 'Abnormality of the upper respiratory tract'),
(110416, 'HP:0001607', 'Subglottic stenosis', 'XPO:0100262', 'abnormal aortic arch 4', 0.43333333333333335, 7.783689670920507, 1.8365544344593274, 'HP:0002087', 'Abnormality of the upper respiratory tract'),
(110417, 'HP:0001607', 'Subglottic stenosis', 'XPO:0130015', 'increased size of the respiratory system', 0.5, 7.241224942262181, 1.9027907060764961, 'HP:0012252', 'Abnormal respiratory system morphology'),
(110418, 'HP:0001607', 'Subglottic stenosis', 'XPO:0100117', 'abnormal aortic arch', 0.4406779661016949, 7.783689670920507, 1.8520530588911377, 'HP:0002087', 'Abnormality of the upper respiratory tract'),
(110419, 'HP:0001607', 'Subglottic stenosis', 'XPO:0127240', 'abnormally localised pharyngeal epithelium', 0.4262295081967213, 7.783689670920507, 1.821438503049814, 'HP:0002087', 'Abnormality of the upper respiratory tract'),
(110420, 'HP:0001607', 'Subglottic stenosis', 'XPO:0127412', 'abnormally localised thyroid primordium', 0.40625, 7.783689670920507, 1.778236184766089, 'HP:0002087', 'Abnormality of the upper respiratory tract'),
(110421, 'HP:0001607', 'Subglottic stenosis', 'XPO:0100586', 'abnormal thyroid primordium', 0.5, 7.783689670920507, 1.9727759212491045, 'HP:0002087', 'Abnormality of the upper respiratory tract'),
(110422, 'HP:0001607', 'Subglottic stenosis', 'XPO:0125232', 'absent pharynx', 0.45614035087719296, 7.783689670920507, 1.8842650921812627, 'HP:0002087', 'Abnormality of the upper respiratory tract'),
(110423, 'HP:0001607', 'Subglottic stenosis', 'XPO:0126855', 'abnormally localised pharynx', 0.4642857142857143, 7.783689670920507, 1.9010144446167851, 'HP:0002087', 'Abnormality of the upper respiratory tract'),
(110424, 'HP:0001607', 'Subglottic stenosis', 'XPO:0100116', 'abnormal aortic arch 1', 0.43333333333333335, 7.783689670920507, 1.8365544344593274, 'HP:0002087', 'Abnormality of the upper respiratory tract'),
(110425, 'HP:0001607', 'Subglottic stenosis', 'XPO:0101949', 'abnormal respiratory system morphology', 0.5853658536585366, 7.241224942262181, 2.058826320955896, 'HP:0012252', 'Abnormal respiratory system morphology'),
(110426, 'HP:0001607', 'Subglottic stenosis', 'XPO:0100210', 'abnormal pulmonary artery', 0.4067796610169492, 7.241224942262181, 1.7162700916117157, 'HP:0012252', 'Abnormal respiratory system morphology'),
(110427, 'HP:0001607', 'Subglottic stenosis', 'XPO:0102507', 'abnormal oropharynx morphology', 0.4126984126984127, 7.783689670920507, 1.7922936065628097, 'HP:0002087', 'Abnormality of the upper respiratory tract'),
(110428, 'HP:0001607', 'Subglottic stenosis', 'XPO:0102436', 'abnormal larynx morphology', 0.625, 11.404694921567193, 2.669819156044, 'HP:0025423', 'Abnormal larynx morphology'),
(110429, 'HP:0002812', 'Coxa vara', 'XPO:0102033', 'abnormal femur morphology', 0.4017857142857143, 10.819732420846037, 2.084997342705723, 'HP:0002823', 'Abnormal femur morphology'),
(110430, 'HP:0006302', 'Dagger-shaped pulp calcifications', 'XPO:0101659', 'abnormal lower jaw morphology', 0.475, 7.312692920701687, 1.8637406303810895, 'UPHENO:0076800', 'abnormal mouth morphology'),
(110431, 'HP:0006302', 'Dagger-shaped pulp calcifications', 'XPO:0130701', 'increased size of the upper jaw', 0.42696629213483145, 7.312692920701687, 1.7669955806035935, 'UPHENO:0076800', 'abnormal mouth morphology'),
(110432, 'HP:0006302', 'Dagger-shaped pulp calcifications', 'XPO:0102890', 'abnormal dentine morphology', 0.5517241379310345, 11.200822588201543, 2.485913149447091, 'HP:0011061', 'Abnormality of dental structure'),
(110433, 'HP:0006302', 'Dagger-shaped pulp calcifications', 'XPO:0129152', 'decreased size of the oral cavity', 0.4666666666666667, 7.884497199543557, 1.9181845652735452, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(110434, 'HP:0006302', 'Dagger-shaped pulp calcifications', 'XPO:0129225', 'decreased size of the upper jaw', 0.42696629213483145, 7.312692920701687, 1.7669955806035935, 'UPHENO:0076800', 'abnormal mouth morphology'),
(110435, 'HP:0006302', 'Dagger-shaped pulp calcifications', 'XPO:0102960', 'abnormal oral epithelium morphology', 0.4177215189873418, 7.312692920701687, 1.7477611949930372, 'UPHENO:0076800', 'abnormal mouth morphology'),
(110436, 'HP:0006302', 'Dagger-shaped pulp calcifications', 'XPO:0128105', 'decreased size of the tongue', 0.42168674698795183, 7.884497199543557, 1.8234001139933984, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(110437, 'HP:0006302', 'Dagger-shaped pulp calcifications', 'XPO:0128510', 'decreased size of the cementum', 0.5052631578947369, 11.200822588201543, 2.3789415696761895, 'HP:0011061', 'Abnormality of dental structure'),
(110438, 'HP:0006302', 'Dagger-shaped pulp calcifications', 'XPO:0102861', 'abnormal cementum morphology', 0.5647058823529412, 11.200822588201543, 2.514989145652344, 'HP:0011061', 'Abnormality of dental structure'),
(110439, 'HP:0006302', 'Dagger-shaped pulp calcifications', 'XPO:0129585', 'increased size of the tongue', 0.41379310344827586, 7.884497199543557, 1.8062531841711362, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(110440, 'HP:0006302', 'Dagger-shaped pulp calcifications', 'XPO:0141830', 'increased width of mouth', 0.4166666666666667, 7.884497199543557, 1.812514045870123, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(110441, 'HP:0006302', 'Dagger-shaped pulp calcifications', 'XPO:0101567', 'abnormal tongue', 0.5, 7.884497199543557, 1.9855096574360394, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(110442, 'HP:0006302', 'Dagger-shaped pulp calcifications', 'XPO:0103096', 'abnormal oral cavity morphology', 0.5, 7.884497199543557, 1.9855096574360394, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(110443, 'HP:0006302', 'Dagger-shaped pulp calcifications', 'XPO:0140639', 'abnormally necrotic upper jaw', 0.4367816091954023, 7.312692920701687, 1.7871904715099365, 'UPHENO:0076800', 'abnormal mouth morphology'),
(110444, 'HP:0006302', 'Dagger-shaped pulp calcifications', 'XPO:0103138', 'abnormal upper jaw morphology', 0.4634146341463415, 7.312692920701687, 1.8408717811057655, 'UPHENO:0076800', 'abnormal mouth morphology'),
(110445, 'HP:0006302', 'Dagger-shaped pulp calcifications', 'XPO:0128880', 'decreased size of the lower jaw', 0.4367816091954023, 7.312692920701687, 1.7871904715099365, 'UPHENO:0076800', 'abnormal mouth morphology'),
(110446, 'HP:0006302', 'Dagger-shaped pulp calcifications', 'XPO:0139736', 'abnormally necrotic tooth', 0.5172413793103449, 9.872199840740173, 2.259714641819142, 'HP:0006482', 'Abnormal dental morphology'),
(110447, 'HP:0006302', 'Dagger-shaped pulp calcifications', 'XPO:0130358', 'increased size of the lower jaw', 0.4367816091954023, 7.312692920701687, 1.7871904715099365, 'UPHENO:0076800', 'abnormal mouth morphology'),
(110448, 'HP:0006302', 'Dagger-shaped pulp calcifications', 'XPO:0131573', 'decreased size of the roof of mouth', 0.4125, 7.312692920701687, 1.7368033365322182, 'UPHENO:0076800', 'abnormal mouth morphology'),
(110449, 'HP:0006302', 'Dagger-shaped pulp calcifications', 'XPO:0129449', 'decreased size of the dentine', 0.4897959183673469, 11.200822588201543, 2.342246183913616, 'HP:0011061', 'Abnormality of dental structure'),
(110450, 'HP:0006302', 'Dagger-shaped pulp calcifications', 'XPO:0140890', 'abnormally necrotic dentine', 0.5, 11.200822588201543, 2.3665188133840753, 'HP:0011061', 'Abnormality of dental structure'),
(110451, 'HP:0006302', 'Dagger-shaped pulp calcifications', 'XPO:0131611', 'increased size of the roof of mouth', 0.4125, 7.312692920701687, 1.7368033365322182, 'UPHENO:0076800', 'abnormal mouth morphology'),
(110452, 'HP:0006302', 'Dagger-shaped pulp calcifications', 'XPO:0103199', 'abnormal tongue morphology', 0.5, 7.884497199543557, 1.9855096574360394, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(110453, 'HP:0006302', 'Dagger-shaped pulp calcifications', 'XPO:0101816', 'abnormal tooth morphology', 0.569620253164557, 9.872199840740173, 2.371371959978762, 'HP:0006482', 'Abnormal dental morphology'),
(110454, 'HP:0006302', 'Dagger-shaped pulp calcifications', 'XPO:0102279', 'abnormal mouth morphology', 0.4714285714285714, 7.312692920701687, 1.856720866716972, 'UPHENO:0076800', 'abnormal mouth morphology'),
(110455, 'HP:0006302', 'Dagger-shaped pulp calcifications', 'XPO:0140789', 'abnormally necrotic roof of mouth', 0.4230769230769231, 7.312692920701687, 1.7589291117884391, 'UPHENO:0076800', 'abnormal mouth morphology'),
(110456, 'HP:0006302', 'Dagger-shaped pulp calcifications', 'XPO:0141006', 'abnormally necrotic cementum', 0.5161290322580645, 11.200822588201543, 2.4043855187849412, 'HP:0011061', 'Abnormality of dental structure'),
(110457, 'HP:0006302', 'Dagger-shaped pulp calcifications', 'XPO:0140897', 'abnormally necrotic lower jaw', 0.4470588235294118, 7.312692920701687, 1.8080939947803472, 'UPHENO:0076800', 'abnormal mouth morphology'),
(110458, 'HP:0006302', 'Dagger-shaped pulp calcifications', 'XPO:0115558', 'abnormally incomplete structure of mouth', 0.4647887323943662, 7.312692920701687, 1.8435990000545652, 'UPHENO:0076800', 'abnormal mouth morphology'),
(110459, 'HP:0006302', 'Dagger-shaped pulp calcifications', 'XPO:0130466', 'increased size of the tooth', 0.4945054945054945, 9.872199840740173, 2.209492490166528, 'HP:0006482', 'Abnormal dental morphology'),
(110460, 'HP:0006302', 'Dagger-shaped pulp calcifications', 'XPO:0127750', 'abnormally localised tongue', 0.44594594594594594, 7.884497199543557, 1.8751158796081413, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(110461, 'HP:0006302', 'Dagger-shaped pulp calcifications', 'XPO:0103735', 'increased size of the mouth', 0.4430379746835443, 7.884497199543557, 1.8689921537245293, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(110462, 'HP:0006302', 'Dagger-shaped pulp calcifications', 'XPO:0128989', 'decreased size of the tooth', 0.4945054945054945, 9.872199840740173, 2.209492490166528, 'HP:0006482', 'Abnormal dental morphology'),
(110463, 'HP:0006302', 'Dagger-shaped pulp calcifications', 'XPO:0103828', 'decreased width of the mouth', 0.4166666666666667, 7.884497199543557, 1.812514045870123, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(110464, 'HP:0006302', 'Dagger-shaped pulp calcifications', 'XPO:0115393', 'abnormally decreased volume of oral cavity', 0.45454545454545453, 7.884497199543557, 1.8931091789510952, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(110465, 'HP:0006302', 'Dagger-shaped pulp calcifications', 'XPO:0141311', 'abnormal roof of mouth morphology', 0.4520547945205479, 7.312692920701687, 1.8181688303509294, 'UPHENO:0076800', 'abnormal mouth morphology'),
(110466, 'HP:0006302', 'Dagger-shaped pulp calcifications', 'XPO:0130628', 'increased size of the oral cavity', 0.4666666666666667, 7.884497199543557, 1.9181845652735452, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(110467, 'HP:0006302', 'Dagger-shaped pulp calcifications', 'XPO:0126089', 'absent tongue', 0.4342105263157895, 7.884497199543557, 1.8502788110847448, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(110468, 'HP:0006302', 'Dagger-shaped pulp calcifications', 'XPO:0103352', 'decreased size of the mouth', 0.4430379746835443, 7.884497199543557, 1.8689921537245293, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(110469, 'HP:0006302', 'Dagger-shaped pulp calcifications', 'XPO:0129990', 'increased size of the cementum', 0.5052631578947369, 11.200822588201543, 2.3789415696761895, 'HP:0011061', 'Abnormality of dental structure'),
(110470, 'HP:0006302', 'Dagger-shaped pulp calcifications', 'XPO:0130923', 'increased size of the dentine', 0.4897959183673469, 11.200822588201543, 2.342246183913616, 'HP:0011061', 'Abnormality of dental structure'),
(110471, 'HP:0006302', 'Dagger-shaped pulp calcifications', 'XPO:0140626', 'abnormally necrotic tongue', 0.4666666666666667, 7.884497199543557, 1.9181845652735452, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(110472, 'HP:0001446', 'Abnormality of the musculature of the upper limbs', 'XPO:0100852', 'abnormal interdigital region', 0.4482758620689655, 5.504475013697824, 1.570835217966058, 'HP:0040064', 'Abnormality of limbs'),
(110473, 'HP:0001446', 'Abnormality of the musculature of the upper limbs', 'XPO:0100751', 'abnormal coracoid bone', 0.41379310344827586, 9.992881323162637, 2.0334663447182453, 'HP:0001446', 'Abnormality of the musculature of the upper limbs'),
(110474, 'HP:0001446', 'Abnormality of the musculature of the upper limbs', 'XPO:0101233', 'abnormal scapula', 0.41379310344827586, 9.992881323162637, 2.0334663447182453, 'HP:0001446', 'Abnormality of the musculature of the upper limbs'),
(110475, 'HP:0001446', 'Abnormality of the musculature of the upper limbs', 'XPO:0100386', 'abnormal limb', 0.41935483870967744, 5.504475013697824, 1.5193183443737854, 'HP:0040064', 'Abnormality of limbs'),
(110476, 'HP:0001446', 'Abnormality of the musculature of the upper limbs', 'XPO:0127441', 'abnormally localised pectoral girdle', 0.47058823529411764, 9.992881323162637, 2.1685323118115285, 'HP:0001446', 'Abnormality of the musculature of the upper limbs'),
(110477, 'HP:0001446', 'Abnormality of the musculature of the upper limbs', 'XPO:0100100', 'abnormal muscle', 0.4117647058823529, 5.968280811662945, 1.5676502776568768, 'UPHENO:0002816', 'abnormal musculature'),
(110478, 'HP:0001446', 'Abnormality of the musculature of the upper limbs', 'XPO:0101732', 'abnormal muscle morphology', 0.4146341463414634, 6.895202660022325, 1.6908537691916898, 'HP:0011805', 'Abnormal skeletal muscle morphology'),
(110479, 'HP:0001446', 'Abnormality of the musculature of the upper limbs', 'XPO:0100768', 'abnormal pectoral girdle', 0.5853658536585366, 9.992881323162637, 2.418572204057911, 'HP:0001446', 'Abnormality of the musculature of the upper limbs'),
(110480, 'HP:0001446', 'Abnormality of the musculature of the upper limbs', 'XPO:0100205', 'abnormal limb segment', 0.40625, 5.504475013697824, 1.4953905758412218, 'HP:0040064', 'Abnormality of limbs'),
(110481, 'HP:0001446', 'Abnormality of the musculature of the upper limbs', 'XPO:0125790', 'absent pectoral girdle', 0.4528301886792453, 9.992881323162637, 2.1272231512037103, 'HP:0001446', 'Abnormality of the musculature of the upper limbs'),
(110482, 'HP:0001446', 'Abnormality of the musculature of the upper limbs', 'XPO:0102400', 'abnormal pectoral girdle morphology', 0.42857142857142855, 9.992881323162637, 2.0694596937878638, 'HP:0001446', 'Abnormality of the musculature of the upper limbs'),
(110483, 'HP:0011354', 'Generalized abnormality of skin', 'XPO:0100081', 'abnormal anatomical entity in vitro', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(110484, 'HP:0011354', 'Generalized abnormality of skin', 'XPO:0101513', 'abnormal basal body', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(110485, 'HP:0011354', 'Generalized abnormality of skin', 'XPO:0100704', 'abnormal Merkel cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(110486, 'HP:0011354', 'Generalized abnormality of skin', 'XPO:0100481', 'abnormal anatomical line', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(110487, 'HP:0011354', 'Generalized abnormality of skin', 'XPO:0100507', 'abnormal skin', 0.5172413793103449, 6.8660902472206855, 1.8845227485869556, 'HP:0000951', 'Abnormality of the skin'),
(110488, 'HP:0011354', 'Generalized abnormality of skin', 'XPO:0100372', 'abnormal hematological system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(110489, 'HP:0011354', 'Generalized abnormality of skin', 'XPO:0100546', 'abnormal whole organism', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(110490, 'HP:0011354', 'Generalized abnormality of skin', 'XPO:0140154', 'abnormally necrotic skin', 0.4090909090909091, 7.420886955069779, 1.7423597190908553, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(110491, 'HP:0011354', 'Generalized abnormality of skin', 'XPO:0100894', 'abnormal nucleus', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(110492, 'HP:0011354', 'Generalized abnormality of skin', 'XPO:0101569', 'abnormal activin-induced ectoderm', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(110493, 'HP:0011354', 'Generalized abnormality of skin', 'XPO:0100852', 'abnormal interdigital region', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(110494, 'HP:0011354', 'Generalized abnormality of skin', 'XPO:0100581', 'abnormal immune system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(110495, 'HP:0011354', 'Generalized abnormality of skin', 'XPO:0102626', 'abnormal granular gland morphology', 0.45, 7.420886955069779, 1.8274022900777487, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(110496, 'HP:0011354', 'Generalized abnormality of skin', 'XPO:0102176', 'abnormal neuromast support cell morphology', 0.43902439024390244, 7.420886955069779, 1.8049793268950312, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(110497, 'HP:0011354', 'Generalized abnormality of skin', 'XPO:0100337', 'abnormal zygote', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(110498, 'HP:0011354', 'Generalized abnormality of skin', 'XPO:0103147', 'abnormal neuromast mantle cell morphology', 0.43902439024390244, 7.420886955069779, 1.8049793268950312, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(110499, 'HP:0011354', 'Generalized abnormality of skin', 'XPO:0100715', 'abnormal ciliated cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(110500, 'HP:0011354', 'Generalized abnormality of skin', 'XPO:0101387', 'abnormal melanophore', 0.4411764705882353, 6.8660902472206855, 1.740447489012273, 'HP:0000951', 'Abnormality of the skin'),
(110501, 'HP:0011354', 'Generalized abnormality of skin', 'XPO:0103019', 'abnormal melanophore morphology', 0.4186046511627907, 7.420886955069779, 1.7625032752155354, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(110502, 'HP:0011354', 'Generalized abnormality of skin', 'XPO:0100674', 'abnormal secondary oogonium', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(110503, 'HP:0011354', 'Generalized abnormality of skin', 'XPO:0100626', 'abnormal primordial germ cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(110504, 'HP:0011354', 'Generalized abnormality of skin', 'XPO:0101326', 'abnormal cementoblast', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(110505, 'HP:0011354', 'Generalized abnormality of skin', 'XPO:0100691', 'abnormal keratin accumulating cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(110506, 'HP:0011354', 'Generalized abnormality of skin', 'XPO:0101004', 'abnormal acid secreting cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(110507, 'HP:0011354', 'Generalized abnormality of skin', 'XPO:0100802', 'abnormal exocrine cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(110508, 'HP:0011354', 'Generalized abnormality of skin', 'XPO:0100888', 'abnormal microtubule', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(110509, 'HP:0011354', 'Generalized abnormality of skin', 'XPO:0101264', 'abnormal mitotic spindle', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(110510, 'HP:0011354', 'Generalized abnormality of skin', 'XPO:0100969', 'abnormal disaggregated/reaggregated ectoderm treated with activin', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(110511, 'HP:0011354', 'Generalized abnormality of skin', 'XPO:0101228', 'abnormal mesenchymal stem cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(110512, 'HP:0011354', 'Generalized abnormality of skin', 'XPO:0100025', 'abnormal oocyte', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(110513, 'HP:0011354', 'Generalized abnormality of skin', 'XPO:0100289', 'abnormal chondroblast', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(110514, 'HP:0011354', 'Generalized abnormality of skin', 'XPO:0103161', 'abnormal skin mucous gland morphology', 0.4090909090909091, 7.420886955069779, 1.7423597190908553, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(110515, 'HP:0011354', 'Generalized abnormality of skin', 'XPO:0101110', 'abnormal cell-free extract', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(110516, 'HP:0011354', 'Generalized abnormality of skin', 'XPO:0101095', 'abnormal skin seromucous gland', 0.4838709677419355, 6.8660902472206855, 1.8227182263109507, 'HP:0000951', 'Abnormality of the skin'),
(110517, 'HP:0011354', 'Generalized abnormality of skin', 'XPO:0101333', 'abnormal barrier epithelial cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(110518, 'HP:0011354', 'Generalized abnormality of skin', 'XPO:0107258', 'abnormal anatomical axis', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(110519, 'HP:0011354', 'Generalized abnormality of skin', 'XPO:0102561', 'abnormal dermis morphology', 0.46153846153846156, 7.420886955069779, 1.8506822386605823, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(110520, 'HP:0011354', 'Generalized abnormality of skin', 'XPO:0102945', 'abnormal Eberth-Kastschenko layer morphology', 0.43902439024390244, 7.420886955069779, 1.8049793268950312, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(110521, 'HP:0011354', 'Generalized abnormality of skin', 'XPO:0100501', 'abnormal urogenital system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(110522, 'HP:0011354', 'Generalized abnormality of skin', 'XPO:0140591', 'abnormally necrotic skin gland', 0.4090909090909091, 7.420886955069779, 1.7423597190908553, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(110523, 'HP:0011354', 'Generalized abnormality of skin', 'XPO:0101241', 'abnormal nucleate erythrocyte', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(110524, 'HP:0011354', 'Generalized abnormality of skin', 'XPO:0100638', 'abnormal polar body', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(110525, 'HP:0011354', 'Generalized abnormality of skin', 'XPO:0100344', 'abnormal portion of organism substance', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(110526, 'HP:0011354', 'Generalized abnormality of skin', 'XPO:0102727', 'abnormal skin seromucous gland morphology', 0.45, 7.420886955069779, 1.8274022900777487, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(110527, 'HP:0011354', 'Generalized abnormality of skin', 'XPO:0100549', 'abnormal mitotic cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(110528, 'HP:0011354', 'Generalized abnormality of skin', 'XPO:0100994', 'abnormal granular gland', 0.4838709677419355, 6.8660902472206855, 1.8227182263109507, 'HP:0000951', 'Abnormality of the skin'),
(110529, 'HP:0011354', 'Generalized abnormality of skin', 'XPO:0101435', 'abnormal paracrine cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(110530, 'HP:0011354', 'Generalized abnormality of skin', 'XPO:0101467', 'abnormal alkali secreting cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(110531, 'HP:0011354', 'Generalized abnormality of skin', 'XPO:0100976', 'abnormal multiciliated cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(110532, 'HP:0011354', 'Generalized abnormality of skin', 'XPO:0107312', 'abnormal filopodium', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(110533, 'HP:0011354', 'Generalized abnormality of skin', 'XPO:0100791', 'abnormal multiciliated cell precursor', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(110534, 'HP:0011354', 'Generalized abnormality of skin', 'XPO:0100317', 'abnormal respiratory system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(110535, 'HP:0011354', 'Generalized abnormality of skin', 'XPO:0102840', 'abnormal stratum spongiosum morphology', 0.43902439024390244, 7.420886955069779, 1.8049793268950312, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(110536, 'HP:0011354', 'Generalized abnormality of skin', 'XPO:0131666', 'abnormal adherens junction', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(110537, 'HP:0011354', 'Generalized abnormality of skin', 'XPO:0100437', 'abnormal proepicardium', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(110538, 'HP:0011354', 'Generalized abnormality of skin', 'XPO:0102886', 'abnormal stratum compactum morphology', 0.43902439024390244, 7.420886955069779, 1.8049793268950312, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(110539, 'HP:0011354', 'Generalized abnormality of skin', 'XPO:0103398', 'abnormally increased number of dense core granule in the goblet cell', 0.40540540540540543, 6.8660902472206855, 1.6683974647021622, 'HP:0000951', 'Abnormality of the skin'),
(110540, 'HP:0011354', 'Generalized abnormality of skin', 'XPO:0102954', 'abnormal iridophore morphology', 0.4186046511627907, 7.420886955069779, 1.7625032752155354, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(110541, 'HP:0011354', 'Generalized abnormality of skin', 'XPO:0101313', 'abnormal Eberth-Kastschenko layer', 0.45454545454545453, 6.8660902472206855, 1.7666211003984522, 'HP:0000951', 'Abnormality of the skin'),
(110542, 'HP:0011354', 'Generalized abnormality of skin', 'XPO:0101448', 'abnormal myelin accumulating cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(110543, 'HP:0011354', 'Generalized abnormality of skin', 'XPO:0100429', 'abnormal spermatid', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(110544, 'HP:0011354', 'Generalized abnormality of skin', 'XPO:0101515', 'abnormal neuromast mantle cell', 0.45454545454545453, 6.8660902472206855, 1.7666211003984522, 'HP:0000951', 'Abnormality of the skin'),
(110545, 'HP:0011354', 'Generalized abnormality of skin', 'XPO:0101547', 'abnormal lampbrush chromosome', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(110546, 'HP:0011354', 'Generalized abnormality of skin', 'XPO:0100172', 'abnormal stem cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(110547, 'HP:0011354', 'Generalized abnormality of skin', 'XPO:0101132', 'abnormal apoptotic cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(110548, 'HP:0011354', 'Generalized abnormality of skin', 'XPO:0140540', 'abnormally necrotic dermis', 0.4090909090909091, 7.420886955069779, 1.7423597190908553, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(110549, 'HP:0011354', 'Generalized abnormality of skin', 'XPO:0101322', 'abnormal iridophore', 0.4411764705882353, 6.8660902472206855, 1.740447489012273, 'HP:0000951', 'Abnormality of the skin'),
(110550, 'HP:0011354', 'Generalized abnormality of skin', 'XPO:0102615', 'abnormal skin gland morphology', 0.47368421052631576, 7.420886955069779, 1.8748751901706053, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(110551, 'HP:0011354', 'Generalized abnormality of skin', 'XPO:0100724', 'abnormal kinetochore', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(110552, 'HP:0011354', 'Generalized abnormality of skin', 'XPO:0100008', 'abnormal epidermis', 0.40540540540540543, 6.8660902472206855, 1.6683974647021622, 'HP:0000951', 'Abnormality of the skin'),
(110553, 'HP:0011354', 'Generalized abnormality of skin', 'XPO:0107284', 'abnormal migrating myoblast', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(110554, 'HP:0011354', 'Generalized abnormality of skin', 'XPO:0101141', 'abnormal Keller explant', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(110555, 'HP:0011354', 'Generalized abnormality of skin', 'XPO:0101240', 'abnormal ciliated non-epidermal cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(110556, 'HP:0011354', 'Generalized abnormality of skin', 'XPO:0100983', 'abnormal skin gland', 0.5, 6.8660902472206855, 1.8528478414619864, 'HP:0000951', 'Abnormality of the skin'),
(110557, 'HP:0011354', 'Generalized abnormality of skin', 'XPO:0100308', 'abnormal early embryonic cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(110558, 'HP:0011354', 'Generalized abnormality of skin', 'XPO:0100721', 'abnormal centromere', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(110559, 'HP:0011354', 'Generalized abnormality of skin', 'XPO:0100907', 'abnormal cytoplasm', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(110560, 'HP:0011354', 'Generalized abnormality of skin', 'XPO:0100956', 'abnormal centrosome', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(110561, 'HP:0011354', 'Generalized abnormality of skin', 'XPO:0101254', 'abnormal stratum compactum', 0.45454545454545453, 6.8660902472206855, 1.7666211003984522, 'HP:0000951', 'Abnormality of the skin'),
(110562, 'HP:0011354', 'Generalized abnormality of skin', 'XPO:0100754', 'abnormal electrically active cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(110563, 'HP:0011354', 'Generalized abnormality of skin', 'XPO:0101278', 'abnormal pigment cell', 0.45454545454545453, 6.8660902472206855, 1.7666211003984522, 'HP:0000951', 'Abnormality of the skin'),
(110564, 'HP:0011354', 'Generalized abnormality of skin', 'XPO:0100108', 'abnormal cell part', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(110565, 'HP:0011354', 'Generalized abnormality of skin', 'XPO:0101014', 'abnormal goblet cell', 0.4166666666666667, 6.8660902472206855, 1.6914109306558096, 'HP:0000951', 'Abnormality of the skin'),
(110566, 'HP:0011354', 'Generalized abnormality of skin', 'XPO:0101071', 'abnormal endoplasmic reticulum', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(110567, 'HP:0011354', 'Generalized abnormality of skin', 'XPO:0103223', 'abnormal xanthophore morphology', 0.4186046511627907, 7.420886955069779, 1.7625032752155354, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(110568, 'HP:0011354', 'Generalized abnormality of skin', 'XPO:0100006', 'abnormal anatomical structure', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(110569, 'HP:0011354', 'Generalized abnormality of skin', 'XPO:0101373', 'abnormal oxygen accumulating cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(110570, 'HP:0011354', 'Generalized abnormality of skin', 'XPO:0100929', 'abnormal dermis', 0.4838709677419355, 6.8660902472206855, 1.8227182263109507, 'HP:0000951', 'Abnormality of the skin'),
(110571, 'HP:0011354', 'Generalized abnormality of skin', 'XPO:0100544', 'abnormal neuromast support cell', 0.45454545454545453, 6.8660902472206855, 1.7666211003984522, 'HP:0000951', 'Abnormality of the skin'),
(110572, 'HP:0011354', 'Generalized abnormality of skin', 'XPO:0131667', 'abnormal actin cytoskeleton', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(110573, 'HP:0011354', 'Generalized abnormality of skin', 'XPO:0100653', 'abnormal myoblast', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(110574, 'HP:0011354', 'Generalized abnormality of skin', 'XPO:0101591', 'abnormal xanthophore', 0.4411764705882353, 6.8660902472206855, 1.740447489012273, 'HP:0000951', 'Abnormality of the skin'),
(110575, 'HP:0011354', 'Generalized abnormality of skin', 'XPO:0101237', 'abnormal mucus secreting cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(110576, 'HP:0011354', 'Generalized abnormality of skin', 'XPO:0101529', 'abnormal skin mucous gland', 0.45454545454545453, 6.8660902472206855, 1.7666211003984522, 'HP:0000951', 'Abnormality of the skin'),
(110577, 'HP:0011354', 'Generalized abnormality of skin', 'XPO:0100232', 'abnormal lymphatic system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(110578, 'HP:0011354', 'Generalized abnormality of skin', 'XPO:0100477', 'abnormal pericyte', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(110579, 'HP:0011354', 'Generalized abnormality of skin', 'XPO:0102910', 'abnormal pigment cell morphology', 0.43902439024390244, 7.420886955069779, 1.8049793268950312, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(110580, 'HP:0011354', 'Generalized abnormality of skin', 'XPO:0100902', 'abnormal spermatocyte', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(110581, 'HP:0011354', 'Generalized abnormality of skin', 'XPO:0102139', 'abnormal skin morphology', 0.47368421052631576, 7.420886955069779, 1.8748751901706053, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(110582, 'HP:0011354', 'Generalized abnormality of skin', 'XPO:0100004', 'abnormal cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(110583, 'HP:0011354', 'Generalized abnormality of skin', 'XPO:0100285', 'abnormal progenitor cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(110584, 'HP:0011354', 'Generalized abnormality of skin', 'XPO:0100225', 'abnormal endocrine system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(110585, 'HP:0011354', 'Generalized abnormality of skin', 'XPO:0100533', 'abnormal melanoblast', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(110586, 'HP:0011354', 'Generalized abnormality of skin', 'XPO:0100026', 'abnormal germ cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(110587, 'HP:0011354', 'Generalized abnormality of skin', 'XPO:0100515', 'abnormal somatic stem cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(110588, 'HP:0011354', 'Generalized abnormality of skin', 'XPO:0100258', 'abnormal organ part', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(110589, 'HP:0011354', 'Generalized abnormality of skin', 'XPO:0100899', 'abnormal secondary spermatogonium', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(110590, 'HP:0011354', 'Generalized abnormality of skin', 'XPO:0101535', 'abnormal absorptive cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(110591, 'HP:0011354', 'Generalized abnormality of skin', 'XPO:0142057', 'abnormal desmosome', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(110592, 'HP:0011354', 'Generalized abnormality of skin', 'XPO:0101061', 'abnormal plasma membrane', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(110593, 'HP:0011354', 'Generalized abnormality of skin', 'XPO:0101297', 'abnormal barrier cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(110594, 'HP:0011354', 'Generalized abnormality of skin', 'XPO:0100032', 'abnormal nervous system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(110595, 'HP:0011354', 'Generalized abnormality of skin', 'XPO:0101208', 'abnormal stratum spongiosum', 0.45454545454545453, 6.8660902472206855, 1.7666211003984522, 'HP:0000951', 'Abnormality of the skin'),
(110596, 'HP:0034628', 'Lymph node xanthomatosis', 'XPO:0126264', 'absent dorsal caudal lymphatic vessel', 0.40816326530612246, 8.696350005340756, 1.8840198020256578, 'UPHENO:0075774', 'abnormal lymphatic part of lymphoid system'),
(110597, 'HP:0034628', 'Lymph node xanthomatosis', 'XPO:0100324', 'abnormal intersomitic vessel', 0.42105263157894735, 5.809304221129108, 1.5639766078650594, 'UPHENO:0002678', 'abnormal vasculature'),
(110598, 'HP:0034628', 'Lymph node xanthomatosis', 'XPO:0100921', 'abnormal dorsal caudal lymphatic vessel', 0.5405405405405406, 8.696350005340756, 2.168116632613805, 'UPHENO:0075774', 'abnormal lymphatic part of lymphoid system'),
(110599, 'HP:0034628', 'Lymph node xanthomatosis', 'XPO:0100599', 'abnormal adult immune system', 0.40625, 5.64885357140806, 1.5148751642906173, 'HP:0002715', 'Abnormality of the immune system'),
(110600, 'HP:0034628', 'Lymph node xanthomatosis', 'XPO:0125762', 'absent lymph vessel', 0.425531914893617, 8.696350005340756, 1.923687726830363, 'UPHENO:0075774', 'abnormal lymphatic part of lymphoid system'),
(110601, 'HP:0034628', 'Lymph node xanthomatosis', 'XPO:0100780', 'abnormal vascular plexus', 0.4444444444444444, 5.809304221129108, 1.6068332169732154, 'UPHENO:0002678', 'abnormal vasculature'),
(110602, 'HP:0034628', 'Lymph node xanthomatosis', 'XPO:0100137', 'abnormal cardinal vein', 0.43243243243243246, 5.809304221129108, 1.5849705218340364, 'UPHENO:0002678', 'abnormal vasculature'),
(110603, 'HP:0034628', 'Lymph node xanthomatosis', 'XPO:0100232', 'abnormal lymphatic system', 0.41935483870967744, 5.64885357140806, 1.5391147060347428, 'HP:0002715', 'Abnormality of the immune system'),
(110604, 'HP:0034628', 'Lymph node xanthomatosis', 'XPO:0102231', 'abnormal adult immune system morphology', 0.41025641025641024, 6.786309419308587, 1.6685703285312263, 'UPHENO:0087123', 'abnormal immune system morphology'),
(110605, 'HP:0034628', 'Lymph node xanthomatosis', 'XPO:0101557', 'abnormal Jacobsons vein', 0.43243243243243246, 5.809304221129108, 1.5849705218340364, 'UPHENO:0002678', 'abnormal vasculature'),
(110606, 'HP:0034628', 'Lymph node xanthomatosis', 'XPO:0100789', 'abnormal occipitovertebral artery', 0.43243243243243246, 5.809304221129108, 1.5849705218340364, 'UPHENO:0002678', 'abnormal vasculature'),
(110607, 'HP:0034628', 'Lymph node xanthomatosis', 'XPO:0102853', 'abnormal larval immune system morphology', 0.41025641025641024, 6.786309419308587, 1.6685703285312263, 'UPHENO:0087123', 'abnormal immune system morphology'),
(110608, 'HP:0034628', 'Lymph node xanthomatosis', 'XPO:0100043', 'abnormal vein', 0.4444444444444444, 5.809304221129108, 1.6068332169732154, 'UPHENO:0002678', 'abnormal vasculature'),
(110609, 'HP:0034628', 'Lymph node xanthomatosis', 'XPO:0101013', 'abnormal ventral caudal lymphatic vessel', 0.5405405405405406, 8.696350005340756, 2.168116632613805, 'UPHENO:0075774', 'abnormal lymphatic part of lymphoid system'),
(110610, 'HP:0034628', 'Lymph node xanthomatosis', 'XPO:0103083', 'abnormal dorsal lymph space morphology', 0.43243243243243246, 6.786309419308587, 1.7130733461912075, 'UPHENO:0087123', 'abnormal immune system morphology'),
(110611, 'HP:0034628', 'Lymph node xanthomatosis', 'XPO:0100792', 'abnormal capillary', 0.4444444444444444, 5.809304221129108, 1.6068332169732154, 'UPHENO:0002678', 'abnormal vasculature'),
(110612, 'HP:0034628', 'Lymph node xanthomatosis', 'XPO:0100987', 'abnormal larval aorta', 0.43243243243243246, 5.809304221129108, 1.5849705218340364, 'UPHENO:0002678', 'abnormal vasculature'),
(110613, 'HP:0034628', 'Lymph node xanthomatosis', 'XPO:0100142', 'abnormal paired dorsal aorta', 0.42105263157894735, 5.809304221129108, 1.5639766078650594, 'UPHENO:0002678', 'abnormal vasculature'),
(110614, 'HP:0034628', 'Lymph node xanthomatosis', 'XPO:0102554', 'abnormal lymph vessel morphology', 0.4489795918367347, 8.696350005340756, 1.975976638492287, 'UPHENO:0075774', 'abnormal lymphatic part of lymphoid system'),
(110615, 'HP:0034628', 'Lymph node xanthomatosis', 'XPO:0102553', 'abnormal dorsal caudal lymphatic vessel morphology', 0.43137254901960786, 8.696350005340756, 1.936844513369755, 'UPHENO:0075774', 'abnormal lymphatic part of lymphoid system'),
(110616, 'HP:0034628', 'Lymph node xanthomatosis', 'XPO:0102645', 'abnormal ventral caudal lymphatic vessel morphology', 0.43137254901960786, 8.696350005340756, 1.936844513369755, 'UPHENO:0075774', 'abnormal lymphatic part of lymphoid system'),
(110617, 'HP:0034628', 'Lymph node xanthomatosis', 'XPO:0100080', 'abnormal aorta', 0.43243243243243246, 5.809304221129108, 1.5849705218340364, 'UPHENO:0002678', 'abnormal vasculature'),
(110618, 'HP:0034628', 'Lymph node xanthomatosis', 'XPO:0127411', 'abnormally localised lymph vessel', 0.4444444444444444, 8.696350005340756, 1.9659716291996978, 'UPHENO:0075774', 'abnormal lymphatic part of lymphoid system'),
(110619, 'HP:0034628', 'Lymph node xanthomatosis', 'XPO:0101585', 'abnormal dorsal longitudinal anastomosing vessel - right branch', 0.43243243243243246, 5.809304221129108, 1.5849705218340364, 'UPHENO:0002678', 'abnormal vasculature'),
(110620, 'HP:0034628', 'Lymph node xanthomatosis', 'XPO:0100980', 'abnormal dorsal longitudinal anastomosing vessel - left branch', 0.43243243243243246, 5.809304221129108, 1.5849705218340364, 'UPHENO:0002678', 'abnormal vasculature'),
(110621, 'HP:0034628', 'Lymph node xanthomatosis', 'XPO:0101864', 'abnormal lymphatic system morphology', 0.43243243243243246, 6.786309419308587, 1.7130733461912075, 'UPHENO:0087123', 'abnormal immune system morphology'),
(110622, 'HP:0034628', 'Lymph node xanthomatosis', 'XPO:0101221', 'abnormal larval immune system', 0.40625, 5.64885357140806, 1.5148751642906173, 'HP:0002715', 'Abnormality of the immune system'),
(110623, 'HP:0034628', 'Lymph node xanthomatosis', 'XPO:0101243', 'abnormal vertebral artery', 0.43243243243243246, 5.809304221129108, 1.5849705218340364, 'UPHENO:0002678', 'abnormal vasculature'),
(110624, 'HP:0034628', 'Lymph node xanthomatosis', 'XPO:0100581', 'abnormal immune system', 0.41935483870967744, 5.64885357140806, 1.5391147060347428, 'HP:0002715', 'Abnormality of the immune system'),
(110625, 'HP:0034628', 'Lymph node xanthomatosis', 'XPO:0140735', 'abnormally necrotic lymph vessel', 0.4074074074074074, 8.696350005340756, 1.8822745308756825, 'UPHENO:0075774', 'abnormal lymphatic part of lymphoid system'),
(110626, 'HP:0034628', 'Lymph node xanthomatosis', 'XPO:0100981', 'abnormal dorsal longitudinal anastomosing vessel', 0.4444444444444444, 5.809304221129108, 1.6068332169732154, 'UPHENO:0002678', 'abnormal vasculature'),
(110627, 'HP:0034628', 'Lymph node xanthomatosis', 'XPO:0101051', 'abnormal intersomitic vein', 0.41025641025641024, 5.809304221129108, 1.5437954190396599, 'UPHENO:0002678', 'abnormal vasculature'),
(110628, 'HP:0034628', 'Lymph node xanthomatosis', 'XPO:0127543', 'abnormally localised ventral caudal lymphatic vessel', 0.425531914893617, 8.696350005340756, 1.923687726830363, 'UPHENO:0075774', 'abnormal lymphatic part of lymphoid system'),
(110629, 'HP:0034628', 'Lymph node xanthomatosis', 'XPO:0100933', 'abnormal branchial vein', 0.43243243243243246, 5.809304221129108, 1.5849705218340364, 'UPHENO:0002678', 'abnormal vasculature'),
(110630, 'HP:0034628', 'Lymph node xanthomatosis', 'XPO:0101583', 'abnormal truncus arteriosus', 0.4444444444444444, 5.809304221129108, 1.6068332169732154, 'UPHENO:0002678', 'abnormal vasculature'),
(110631, 'HP:0034628', 'Lymph node xanthomatosis', 'XPO:0127928', 'abnormally localised dorsal caudal lymphatic vessel', 0.425531914893617, 8.696350005340756, 1.923687726830363, 'UPHENO:0075774', 'abnormal lymphatic part of lymphoid system'),
(110632, 'HP:0034628', 'Lymph node xanthomatosis', 'XPO:0101431', 'abnormal ischiadic artery', 0.43243243243243246, 5.809304221129108, 1.5849705218340364, 'UPHENO:0002678', 'abnormal vasculature'),
(110633, 'HP:0034628', 'Lymph node xanthomatosis', 'XPO:0101206', 'abnormal ischiadic vein', 0.43243243243243246, 5.809304221129108, 1.5849705218340364, 'UPHENO:0002678', 'abnormal vasculature'),
(110634, 'HP:0034628', 'Lymph node xanthomatosis', 'XPO:0100922', 'abnormal lymph vessel', 0.5555555555555556, 8.696350005340756, 2.1980231023632673, 'UPHENO:0075774', 'abnormal lymphatic part of lymphoid system'),
(110635, 'HP:0034628', 'Lymph node xanthomatosis', 'XPO:0100522', 'abnormal subinterstitial vein', 0.43243243243243246, 5.809304221129108, 1.5849705218340364, 'UPHENO:0002678', 'abnormal vasculature'),
(110636, 'HP:0034628', 'Lymph node xanthomatosis', 'XPO:0102213', 'abnormal immune system morphology', 0.43243243243243246, 6.786309419308587, 1.7130733461912075, 'UPHENO:0087123', 'abnormal immune system morphology'),
(110637, 'HP:0034628', 'Lymph node xanthomatosis', 'XPO:0100659', 'abnormal anterior cardinal vein', 0.42105263157894735, 5.809304221129108, 1.5639766078650594, 'UPHENO:0002678', 'abnormal vasculature'),
(110638, 'HP:0034628', 'Lymph node xanthomatosis', 'XPO:0100054', 'abnormal blood vessel', 0.45714285714285713, 5.809304221129108, 1.6296263159568272, 'UPHENO:0002678', 'abnormal vasculature'),
(110639, 'HP:0034628', 'Lymph node xanthomatosis', 'XPO:0100076', 'abnormal artery', 0.4444444444444444, 5.809304221129108, 1.6068332169732154, 'UPHENO:0002678', 'abnormal vasculature'),
(110640, 'HP:0034628', 'Lymph node xanthomatosis', 'XPO:0125889', 'absent ventral caudal lymphatic vessel', 0.40816326530612246, 8.696350005340756, 1.8840198020256578, 'UPHENO:0075774', 'abnormal lymphatic part of lymphoid system'),
(110641, 'HP:0009413', 'Enlarged epiphyses of the 3rd finger', 'XPO:0103755', 'increased size of the forelimb digit', 0.4166666666666667, 7.492661022682715, 1.7669018345070744, 'HP:0001167', 'Abnormal finger morphology'),
(110642, 'HP:0009413', 'Enlarged epiphyses of the 3rd finger', 'XPO:0115788', 'duplicated forelimb digit 4 in regenerating forelimb', 0.41605839416058393, 7.774297771301195, 1.7984887673971672, 'HP:0005918', 'Abnormal finger phalanx morphology'),
(110643, 'HP:0009413', 'Enlarged epiphyses of the 3rd finger', 'XPO:0102598', 'abnormal forelimb digit 3 morphology', 0.40869565217391307, 7.492661022682715, 1.7499194219115835, 'HP:0001167', 'Abnormal finger morphology'),
(110644, 'HP:0009413', 'Enlarged epiphyses of the 3rd finger', 'XPO:0103634', 'abnormally increased number of forelimb digit', 0.4523809523809524, 7.774297771301195, 1.875351761636827, 'HP:0005918', 'Abnormal finger phalanx morphology'),
(110645, 'HP:0009413', 'Enlarged epiphyses of the 3rd finger', 'XPO:0130624', 'increased size of the forelimb digit 4', 0.4065040650406504, 7.492661022682715, 1.7452212363170925, 'HP:0001167', 'Abnormal finger morphology'),
(110646, 'HP:0009413', 'Enlarged epiphyses of the 3rd finger', 'XPO:0130664', 'increased size of the forelimb digit 2', 0.4065040650406504, 7.492661022682715, 1.7452212363170925, 'HP:0001167', 'Abnormal finger morphology'),
(110647, 'HP:0009413', 'Enlarged epiphyses of the 3rd finger', 'XPO:0115789', 'duplicated forelimb digit 5 in regenerating forelimb', 0.41605839416058393, 7.774297771301195, 1.7984887673971672, 'HP:0005918', 'Abnormal finger phalanx morphology'),
(110648, 'HP:0009413', 'Enlarged epiphyses of the 3rd finger', 'XPO:0102746', 'abnormal forelimb digit 2 morphology', 0.40869565217391307, 7.492661022682715, 1.7499194219115835, 'HP:0001167', 'Abnormal finger morphology'),
(110649, 'HP:0009413', 'Enlarged epiphyses of the 3rd finger', 'XPO:0102214', 'abnormal forelimb digit morphology', 0.415929203539823, 7.492661022682715, 1.7653375120804229, 'HP:0001167', 'Abnormal finger morphology'),
(110650, 'HP:0009413', 'Enlarged epiphyses of the 3rd finger', 'XPO:0102529', 'abnormal forelimb digit 4 morphology', 0.40869565217391307, 7.492661022682715, 1.7499194219115835, 'HP:0001167', 'Abnormal finger morphology'),
(110651, 'HP:0009413', 'Enlarged epiphyses of the 3rd finger', 'XPO:0129652', 'increased size of the forelimb digit 3', 0.4065040650406504, 7.492661022682715, 1.7452212363170925, 'HP:0001167', 'Abnormal finger morphology'),
(110652, 'HP:0009413', 'Enlarged epiphyses of the 3rd finger', 'XPO:0130637', 'increased size of the forelimb digit 5', 0.4065040650406504, 7.492661022682715, 1.7452212363170925, 'HP:0001167', 'Abnormal finger morphology'),
(110653, 'HP:0009413', 'Enlarged epiphyses of the 3rd finger', 'XPO:0115787', 'duplicated forelimb digit 3 in regenerating forelimb', 0.41605839416058393, 7.774297771301195, 1.7984887673971672, 'HP:0005918', 'Abnormal finger phalanx morphology'),
(110654, 'HP:0009413', 'Enlarged epiphyses of the 3rd finger', 'XPO:0115786', 'duplicated forelimb digit 2 in regenerating forelimb', 0.41605839416058393, 7.774297771301195, 1.7984887673971672, 'HP:0005918', 'Abnormal finger phalanx morphology'),
(110655, 'HP:0009413', 'Enlarged epiphyses of the 3rd finger', 'XPO:0103609', 'abnormally increased number of forelimb digit in the regenerating forelimb', 0.4318181818181818, 7.774297771301195, 1.8322344633033256, 'HP:0005918', 'Abnormal finger phalanx morphology'),
(110656, 'HP:0009413', 'Enlarged epiphyses of the 3rd finger', 'XPO:0102787', 'abnormal forelimb digit 5 morphology', 0.40869565217391307, 7.492661022682715, 1.7499194219115835, 'HP:0001167', 'Abnormal finger morphology'),
(110657, 'HP:0012589', 'Multidrug-resistant nephrotic syndrome', 'XPO:0127342', 'abnormally localised mesonephric mesenchyme', 0.40816326530612246, 6.880013295263146, 1.6757591390006326, 'HP:0000077', 'Abnormality of the kidney'),
(110658, 'HP:0012589', 'Multidrug-resistant nephrotic syndrome', 'XPO:0126072', 'absent mesonephric sinus', 0.43478260869565216, 6.880013295263146, 1.7295404384908961, 'HP:0000077', 'Abnormality of the kidney'),
(110659, 'HP:0012589', 'Multidrug-resistant nephrotic syndrome', 'XPO:0100085', 'abnormal mesonephric sinus', 0.5277777777777778, 6.880013295263146, 1.9055492982485522, 'HP:0000077', 'Abnormality of the kidney'),
(110660, 'HP:0012589', 'Multidrug-resistant nephrotic syndrome', 'XPO:0100566', 'abnormal kidney', 0.475, 6.880013295263146, 1.8077627928602786, 'HP:0000077', 'Abnormality of the kidney'),
(110661, 'HP:0012589', 'Multidrug-resistant nephrotic syndrome', 'XPO:0101717', 'abnormal mesonephric sinus morphology', 0.4444444444444444, 6.880013295263146, 1.7486519627369022, 'HP:0000077', 'Abnormality of the kidney'),
(110662, 'HP:0012589', 'Multidrug-resistant nephrotic syndrome', 'XPO:0107301', 'abnormal adult kidney', 0.4634146341463415, 6.880013295263146, 1.7855808142300187, 'HP:0000077', 'Abnormality of the kidney'),
(110663, 'HP:0012589', 'Multidrug-resistant nephrotic syndrome', 'XPO:0141613', 'metaplastic kidney', 0.46511627906976744, 6.880013295263146, 1.788856110435751, 'HP:0000077', 'Abnormality of the kidney'),
(110664, 'HP:0012589', 'Multidrug-resistant nephrotic syndrome', 'XPO:0100761', 'abnormal ureter', 0.425, 6.828345551150745, 1.703539509151187, 'HP:0010935', 'Abnormality of the upper urinary tract'),
(110665, 'HP:0012589', 'Multidrug-resistant nephrotic syndrome', 'XPO:0100069', 'abnormal urinary system', 0.42857142857142855, 6.355235291121788, 1.6503551943819923, 'HP:0000079', 'Abnormality of the urinary system'),
(110666, 'HP:0012589', 'Multidrug-resistant nephrotic syndrome', 'XPO:0100271', 'abnormal mesonephric nephron', 0.40425531914893614, 6.880013295263146, 1.6677175931270638, 'HP:0000077', 'Abnormality of the kidney'),
(110667, 'HP:0012589', 'Multidrug-resistant nephrotic syndrome', 'XPO:0100778', 'abnormal mesonephric kidney', 0.41304347826086957, 6.880013295263146, 1.685747496500148, 'HP:0000077', 'Abnormality of the kidney'),
(110668, 'HP:0012589', 'Multidrug-resistant nephrotic syndrome', 'XPO:0100147', 'abnormal mesonephric mesenchyme', 0.48717948717948717, 6.880013295263146, 1.83079254667872, 'HP:0000077', 'Abnormality of the kidney'),
(110669, 'HP:0012589', 'Multidrug-resistant nephrotic syndrome', 'XPO:0127733', 'abnormally localised mesonephric sinus', 0.47619047619047616, 6.880013295263146, 1.8100267421417189, 'HP:0000077', 'Abnormality of the kidney'),
(110670, 'HP:0012589', 'Multidrug-resistant nephrotic syndrome', 'XPO:0107300', 'abnormal embryonic kidney', 0.4634146341463415, 6.880013295263146, 1.7855808142300187, 'HP:0000077', 'Abnormality of the kidney'),
(110671, 'HP:0009843', 'Aplasia/Hypoplasia of the middle phalanges of the hand', 'XPO:0103822', 'decreased length of forelimb digit 3 in regenerating forelimb', 0.4122137404580153, 10.200822588201543, 2.0505899723814047, 'HP:0005927', 'Aplasia/hypoplasia involving bones of the hand'),
(110672, 'HP:0009843', 'Aplasia/Hypoplasia of the middle phalanges of the hand', 'XPO:0103609', 'abnormally increased number of forelimb digit in the regenerating forelimb', 0.4789915966386555, 7.774297771301195, 1.929721042591364, 'HP:0005918', 'Abnormal finger phalanx morphology'),
(110673, 'HP:0009843', 'Aplasia/Hypoplasia of the middle phalanges of the hand', 'XPO:0103279', 'absent forelimb digit 2', 0.452991452991453, 10.200822588201543, 2.1496244895184486, 'HP:0005927', 'Aplasia/hypoplasia involving bones of the hand'),
(110674, 'HP:0009843', 'Aplasia/Hypoplasia of the middle phalanges of the hand', 'XPO:0115789', 'duplicated forelimb digit 5 in regenerating forelimb', 0.4596774193548387, 7.774297771301195, 1.8904150699800844, 'HP:0005918', 'Abnormal finger phalanx morphology'),
(110675, 'HP:0009843', 'Aplasia/Hypoplasia of the middle phalanges of the hand', 'XPO:0130624', 'increased size of the forelimb digit 4', 0.415929203539823, 7.492661022682715, 1.7653375120804229, 'HP:0001167', 'Abnormal finger morphology'),
(110676, 'HP:0009843', 'Aplasia/Hypoplasia of the middle phalanges of the hand', 'XPO:0129188', 'decreased size of the forelimb digit 2', 0.41228070175438597, 7.492661022682715, 1.7575777491876043, 'HP:0001167', 'Abnormal finger morphology'),
(110677, 'HP:0009843', 'Aplasia/Hypoplasia of the middle phalanges of the hand', 'XPO:0115787', 'duplicated forelimb digit 3 in regenerating forelimb', 0.4596774193548387, 7.774297771301195, 1.8904150699800844, 'HP:0005918', 'Abnormal finger phalanx morphology'),
(110678, 'HP:0009843', 'Aplasia/Hypoplasia of the middle phalanges of the hand', 'XPO:0130664', 'increased size of the forelimb digit 2', 0.415929203539823, 7.492661022682715, 1.7653375120804229, 'HP:0001167', 'Abnormal finger morphology'),
(110679, 'HP:0009843', 'Aplasia/Hypoplasia of the middle phalanges of the hand', 'XPO:0102787', 'abnormal forelimb digit 5 morphology', 0.46078431372549017, 7.492661022682715, 1.8580905971761936, 'HP:0001167', 'Abnormal finger morphology'),
(110680, 'HP:0009843', 'Aplasia/Hypoplasia of the middle phalanges of the hand', 'XPO:0103755', 'increased size of the forelimb digit', 0.42727272727272725, 7.492661022682715, 1.7892483644513149, 'HP:0001167', 'Abnormal finger morphology'),
(110681, 'HP:0009843', 'Aplasia/Hypoplasia of the middle phalanges of the hand', 'XPO:0103432', 'decreased size of the forelimb digit', 0.42342342342342343, 7.492661022682715, 1.781170452476563, 'HP:0001167', 'Abnormal finger morphology'),
(110682, 'HP:0009843', 'Aplasia/Hypoplasia of the middle phalanges of the hand', 'XPO:0103634', 'abnormally increased number of forelimb digit', 0.504424778761062, 7.774297771301195, 1.9802899871764292, 'HP:0005918', 'Abnormal finger phalanx morphology'),
(110683, 'HP:0009843', 'Aplasia/Hypoplasia of the middle phalanges of the hand', 'XPO:0129148', 'decreased size of the forelimb digit 4', 0.41228070175438597, 7.492661022682715, 1.7575777491876043, 'HP:0001167', 'Abnormal finger morphology'),
(110684, 'HP:0009843', 'Aplasia/Hypoplasia of the middle phalanges of the hand', 'XPO:0140898', 'abnormally necrotic forelimb digit 5', 0.42342342342342343, 7.492661022682715, 1.781170452476563, 'HP:0001167', 'Abnormal finger morphology'),
(110685, 'HP:0009843', 'Aplasia/Hypoplasia of the middle phalanges of the hand', 'XPO:0103280', 'absent forelimb digit 3', 0.452991452991453, 10.200822588201543, 2.1496244895184486, 'HP:0005927', 'Aplasia/hypoplasia involving bones of the hand'),
(110686, 'HP:0009843', 'Aplasia/Hypoplasia of the middle phalanges of the hand', 'XPO:0103824', 'decreased length of forelimb digit 5 in regenerating forelimb', 0.4122137404580153, 10.200822588201543, 2.0505899723814047, 'HP:0005927', 'Aplasia/hypoplasia involving bones of the hand'),
(110687, 'HP:0009843', 'Aplasia/Hypoplasia of the middle phalanges of the hand', 'XPO:0130637', 'increased size of the forelimb digit 5', 0.415929203539823, 7.492661022682715, 1.7653375120804229, 'HP:0001167', 'Abnormal finger morphology'),
(110688, 'HP:0009843', 'Aplasia/Hypoplasia of the middle phalanges of the hand', 'XPO:0140219', 'abnormally necrotic forelimb digit', 0.4351851851851852, 7.492661022682715, 1.8057394813997938, 'HP:0001167', 'Abnormal finger morphology'),
(110689, 'HP:0009843', 'Aplasia/Hypoplasia of the middle phalanges of the hand', 'XPO:0140716', 'abnormally necrotic forelimb digit 4', 0.42342342342342343, 7.492661022682715, 1.781170452476563, 'HP:0001167', 'Abnormal finger morphology'),
(110690, 'HP:0009843', 'Aplasia/Hypoplasia of the middle phalanges of the hand', 'XPO:0141143', 'abnormally necrotic forelimb digit 3', 0.42342342342342343, 7.492661022682715, 1.781170452476563, 'HP:0001167', 'Abnormal finger morphology'),
(110691, 'HP:0009843', 'Aplasia/Hypoplasia of the middle phalanges of the hand', 'XPO:0102214', 'abnormal forelimb digit morphology', 0.47, 7.492661022682715, 1.8765795162105112, 'HP:0001167', 'Abnormal finger morphology'),
(110692, 'HP:0009843', 'Aplasia/Hypoplasia of the middle phalanges of the hand', 'XPO:0125257', 'absent forelimb digit', 0.4649122807017544, 10.200822588201543, 2.177725348733112, 'HP:0005927', 'Aplasia/hypoplasia involving bones of the hand'),
(110693, 'HP:0009843', 'Aplasia/Hypoplasia of the middle phalanges of the hand', 'XPO:0102529', 'abnormal forelimb digit 4 morphology', 0.46078431372549017, 7.492661022682715, 1.8580905971761936, 'HP:0001167', 'Abnormal finger morphology'),
(110694, 'HP:0009843', 'Aplasia/Hypoplasia of the middle phalanges of the hand', 'XPO:0103282', 'absent forelimb digit 5', 0.452991452991453, 10.200822588201543, 2.1496244895184486, 'HP:0005927', 'Aplasia/hypoplasia involving bones of the hand'),
(110695, 'HP:0009843', 'Aplasia/Hypoplasia of the middle phalanges of the hand', 'XPO:0129652', 'increased size of the forelimb digit 3', 0.415929203539823, 7.492661022682715, 1.7653375120804229, 'HP:0001167', 'Abnormal finger morphology'),
(110696, 'HP:0009843', 'Aplasia/Hypoplasia of the middle phalanges of the hand', 'XPO:0133378', 'fused forelimb digits part of regenerating forelimb', 0.4051724137931034, 7.492661022682715, 1.7423603393941962, 'HP:0001167', 'Abnormal finger morphology'),
(110697, 'HP:0009843', 'Aplasia/Hypoplasia of the middle phalanges of the hand', 'XPO:0115786', 'duplicated forelimb digit 2 in regenerating forelimb', 0.4596774193548387, 7.774297771301195, 1.8904150699800844, 'HP:0005918', 'Abnormal finger phalanx morphology'),
(110698, 'HP:0009843', 'Aplasia/Hypoplasia of the middle phalanges of the hand', 'XPO:0141108', 'abnormally necrotic forelimb digit 2', 0.42342342342342343, 7.492661022682715, 1.781170452476563, 'HP:0001167', 'Abnormal finger morphology'),
(110699, 'HP:0009843', 'Aplasia/Hypoplasia of the middle phalanges of the hand', 'XPO:0103821', 'decreased length of forelimb digit 2 in regenerating forelimb', 0.4122137404580153, 10.200822588201543, 2.0505899723814047, 'HP:0005927', 'Aplasia/hypoplasia involving bones of the hand'),
(110700, 'HP:0009843', 'Aplasia/Hypoplasia of the middle phalanges of the hand', 'XPO:0133358', 'fused forelimb digits', 0.43119266055045874, 7.492661022682715, 1.7974371869340195, 'HP:0001167', 'Abnormal finger morphology'),
(110701, 'HP:0009843', 'Aplasia/Hypoplasia of the middle phalanges of the hand', 'XPO:0102746', 'abnormal forelimb digit 2 morphology', 0.46078431372549017, 7.492661022682715, 1.8580905971761936, 'HP:0001167', 'Abnormal finger morphology'),
(110702, 'HP:0009843', 'Aplasia/Hypoplasia of the middle phalanges of the hand', 'XPO:0103281', 'absent forelimb digit 4', 0.452991452991453, 10.200822588201543, 2.1496244895184486, 'HP:0005927', 'Aplasia/hypoplasia involving bones of the hand'),
(110703, 'HP:0009843', 'Aplasia/Hypoplasia of the middle phalanges of the hand', 'XPO:0102598', 'abnormal forelimb digit 3 morphology', 0.46078431372549017, 7.492661022682715, 1.8580905971761936, 'HP:0001167', 'Abnormal finger morphology'),
(110704, 'HP:0009843', 'Aplasia/Hypoplasia of the middle phalanges of the hand', 'XPO:0129161', 'decreased size of the forelimb digit 5', 0.41228070175438597, 7.492661022682715, 1.7575777491876043, 'HP:0001167', 'Abnormal finger morphology'),
(110705, 'HP:0009843', 'Aplasia/Hypoplasia of the middle phalanges of the hand', 'XPO:0141556', 'abnormal forelimb digit morphology in the regenerating forelimb', 0.44339622641509435, 7.492661022682715, 1.822695153684504, 'HP:0001167', 'Abnormal finger morphology'),
(110706, 'HP:0009843', 'Aplasia/Hypoplasia of the middle phalanges of the hand', 'XPO:0128172', 'decreased size of the forelimb digit 3', 0.41228070175438597, 7.492661022682715, 1.7575777491876043, 'HP:0001167', 'Abnormal finger morphology'),
(110707, 'HP:0009843', 'Aplasia/Hypoplasia of the middle phalanges of the hand', 'XPO:0103823', 'decreased length of forelimb digit 4 in regenerating forelimb', 0.4122137404580153, 10.200822588201543, 2.0505899723814047, 'HP:0005927', 'Aplasia/hypoplasia involving bones of the hand'),
(110708, 'HP:0009843', 'Aplasia/Hypoplasia of the middle phalanges of the hand', 'XPO:0115788', 'duplicated forelimb digit 4 in regenerating forelimb', 0.4596774193548387, 7.774297771301195, 1.8904150699800844, 'HP:0005918', 'Abnormal finger phalanx morphology'),
(110709, 'HP:0012131', 'Abnormal number of erythroid precursors', 'XPO:0102386', 'abnormal electrically active cell morphology', 0.42857142857142855, 5.43643956286526, 1.526401870347189, 'HP:0025461', 'Abnormal cell morphology'),
(110710, 'HP:0012131', 'Abnormal number of erythroid precursors', 'XPO:0102869', 'abnormal mucus secreting cell morphology', 0.42857142857142855, 5.43643956286526, 1.526401870347189, 'HP:0025461', 'Abnormal cell morphology'),
(110711, 'HP:0012131', 'Abnormal number of erythroid precursors', 'XPO:0103167', 'abnormal absorptive cell morphology', 0.42857142857142855, 5.43643956286526, 1.526401870347189, 'HP:0025461', 'Abnormal cell morphology'),
(110712, 'HP:0012131', 'Abnormal number of erythroid precursors', 'XPO:0102336', 'abnormal Merkel cell morphology', 0.42857142857142855, 5.43643956286526, 1.526401870347189, 'HP:0025461', 'Abnormal cell morphology'),
(110713, 'HP:0012131', 'Abnormal number of erythroid precursors', 'XPO:0102965', 'abnormal barrier epithelial cell morphology', 0.42857142857142855, 5.43643956286526, 1.526401870347189, 'HP:0025461', 'Abnormal cell morphology'),
(110714, 'HP:0012131', 'Abnormal number of erythroid precursors', 'XPO:0102323', 'abnormal keratin accumulating cell morphology', 0.42857142857142855, 5.43643956286526, 1.526401870347189, 'HP:0025461', 'Abnormal cell morphology'),
(110715, 'HP:0012131', 'Abnormal number of erythroid precursors', 'XPO:0102873', 'abnormal nucleate erythrocyte morphology', 0.42857142857142855, 5.43643956286526, 1.526401870347189, 'HP:0025461', 'Abnormal cell morphology'),
(110716, 'HP:0012131', 'Abnormal number of erythroid precursors', 'XPO:0101940', 'abnormal early embryonic cell morphology', 0.4090909090909091, 5.43643956286526, 1.491307481034791, 'HP:0025461', 'Abnormal cell morphology'),
(110717, 'HP:0012131', 'Abnormal number of erythroid precursors', 'XPO:0101657', 'abnormal oocyte morphology', 0.4090909090909091, 5.43643956286526, 1.491307481034791, 'HP:0025461', 'Abnormal cell morphology'),
(110718, 'HP:0012131', 'Abnormal number of erythroid precursors', 'XPO:0101921', 'abnormal chondroblast morphology', 0.42857142857142855, 5.43643956286526, 1.526401870347189, 'HP:0025461', 'Abnormal cell morphology'),
(110719, 'HP:0012131', 'Abnormal number of erythroid precursors', 'XPO:0103080', 'abnormal myelin accumulating cell morphology', 0.42857142857142855, 5.43643956286526, 1.526401870347189, 'HP:0025461', 'Abnormal cell morphology'),
(110720, 'HP:0012131', 'Abnormal number of erythroid precursors', 'XPO:0102434', 'abnormal exocrine cell morphology', 0.42857142857142855, 5.43643956286526, 1.526401870347189, 'HP:0025461', 'Abnormal cell morphology'),
(110721, 'HP:0012131', 'Abnormal number of erythroid precursors', 'XPO:0102347', 'abnormal ciliated cell morphology', 0.42857142857142855, 5.43643956286526, 1.526401870347189, 'HP:0025461', 'Abnormal cell morphology'),
(110722, 'HP:0012131', 'Abnormal number of erythroid precursors', 'XPO:0102258', 'abnormal primordial germ cell morphology', 0.4090909090909091, 5.43643956286526, 1.491307481034791, 'HP:0025461', 'Abnormal cell morphology'),
(110723, 'HP:0012131', 'Abnormal number of erythroid precursors', 'XPO:0101917', 'abnormal progenitor cell morphology', 0.42857142857142855, 5.43643956286526, 1.526401870347189, 'HP:0025461', 'Abnormal cell morphology'),
(110724, 'HP:0012131', 'Abnormal number of erythroid precursors', 'XPO:0102534', 'abnormal spermatocyte morphology', 0.4090909090909091, 5.43643956286526, 1.491307481034791, 'HP:0025461', 'Abnormal cell morphology'),
(110725, 'HP:0012131', 'Abnormal number of erythroid precursors', 'XPO:0103067', 'abnormal paracrine cell morphology', 0.42857142857142855, 5.43643956286526, 1.526401870347189, 'HP:0025461', 'Abnormal cell morphology'),
(110726, 'HP:0012131', 'Abnormal number of erythroid precursors', 'XPO:0101636', 'abnormal cell morphology', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(110727, 'HP:0012131', 'Abnormal number of erythroid precursors', 'XPO:0103099', 'abnormal alkali secreting cell morphology', 0.42857142857142855, 5.43643956286526, 1.526401870347189, 'HP:0025461', 'Abnormal cell morphology'),
(110728, 'HP:0012131', 'Abnormal number of erythroid precursors', 'XPO:0102860', 'abnormal mesenchymal stem cell morphology', 0.4090909090909091, 5.43643956286526, 1.491307481034791, 'HP:0025461', 'Abnormal cell morphology'),
(110729, 'HP:0012131', 'Abnormal number of erythroid precursors', 'XPO:0102764', 'abnormal apoptotic cell morphology', 0.42857142857142855, 5.43643956286526, 1.526401870347189, 'HP:0025461', 'Abnormal cell morphology'),
(110730, 'HP:0012131', 'Abnormal number of erythroid precursors', 'XPO:0102061', 'abnormal spermatid morphology', 0.4090909090909091, 5.43643956286526, 1.491307481034791, 'HP:0025461', 'Abnormal cell morphology'),
(110731, 'HP:0012131', 'Abnormal number of erythroid precursors', 'XPO:0101969', 'abnormal zygote morphology', 0.42857142857142855, 5.43643956286526, 1.526401870347189, 'HP:0025461', 'Abnormal cell morphology'),
(110732, 'HP:0012131', 'Abnormal number of erythroid precursors', 'XPO:0107371', 'abnormal migrating myoblast morphology', 0.4090909090909091, 5.43643956286526, 1.491307481034791, 'HP:0025461', 'Abnormal cell morphology'),
(110733, 'HP:0012131', 'Abnormal number of erythroid precursors', 'XPO:0103219', 'abnormal hemangioblast morphology', 0.43478260869565216, 5.574066539846944, 1.5567617644449654, 'HP:0001871', 'Abnormality of blood and blood-forming tissues'),
(110734, 'HP:0012131', 'Abnormal number of erythroid precursors', 'XPO:0102109', 'abnormal pericyte morphology', 0.42857142857142855, 5.43643956286526, 1.526401870347189, 'HP:0025461', 'Abnormal cell morphology'),
(110735, 'HP:0012131', 'Abnormal number of erythroid precursors', 'XPO:0103082', 'abnormal myeloid cell morphology', 0.43478260869565216, 5.574066539846944, 1.5567617644449654, 'HP:0001871', 'Abnormality of blood and blood-forming tissues'),
(110736, 'HP:0012131', 'Abnormal number of erythroid precursors', 'XPO:0102872', 'abnormal ciliated non-epidermal cell morphology', 0.4090909090909091, 5.43643956286526, 1.491307481034791, 'HP:0025461', 'Abnormal cell morphology'),
(110737, 'HP:0012131', 'Abnormal number of erythroid precursors', 'XPO:0102423', 'abnormal multiciliated cell precursor morphology', 0.42857142857142855, 5.43643956286526, 1.526401870347189, 'HP:0025461', 'Abnormal cell morphology'),
(110738, 'HP:0012131', 'Abnormal number of erythroid precursors', 'XPO:0102069', 'abnormal proepicardium morphology', 0.4090909090909091, 5.43643956286526, 1.491307481034791, 'HP:0025461', 'Abnormal cell morphology'),
(110739, 'HP:0012131', 'Abnormal number of erythroid precursors', 'XPO:0101804', 'abnormal stem cell morphology', 0.42857142857142855, 5.43643956286526, 1.526401870347189, 'HP:0025461', 'Abnormal cell morphology'),
(110740, 'HP:0012131', 'Abnormal number of erythroid precursors', 'XPO:0102306', 'abnormal secondary oogonium morphology', 0.4090909090909091, 5.43643956286526, 1.491307481034791, 'HP:0025461', 'Abnormal cell morphology'),
(110741, 'HP:0012131', 'Abnormal number of erythroid precursors', 'XPO:0102739', 'abnormal erythroid cell morphology', 0.43478260869565216, 5.574066539846944, 1.5567617644449654, 'HP:0001871', 'Abnormality of blood and blood-forming tissues'),
(110742, 'HP:0012131', 'Abnormal number of erythroid precursors', 'XPO:0102636', 'abnormal acid secreting cell morphology', 0.42857142857142855, 5.43643956286526, 1.526401870347189, 'HP:0025461', 'Abnormal cell morphology'),
(110743, 'HP:0012131', 'Abnormal number of erythroid precursors', 'XPO:0102285', 'abnormal myoblast morphology', 0.42857142857142855, 5.43643956286526, 1.526401870347189, 'HP:0025461', 'Abnormal cell morphology'),
(110744, 'HP:0012131', 'Abnormal number of erythroid precursors', 'XPO:0102165', 'abnormal melanoblast morphology', 0.42857142857142855, 5.43643956286526, 1.526401870347189, 'HP:0025461', 'Abnormal cell morphology'),
(110745, 'HP:0012131', 'Abnormal number of erythroid precursors', 'XPO:0102958', 'abnormal cementoblast morphology', 0.42857142857142855, 5.43643956286526, 1.526401870347189, 'HP:0025461', 'Abnormal cell morphology'),
(110746, 'HP:0012131', 'Abnormal number of erythroid precursors', 'XPO:0139717', 'abnormally necrotic cell', 0.4186046511627907, 5.43643956286526, 1.5085486027240909, 'HP:0025461', 'Abnormal cell morphology'),
(110747, 'HP:0012131', 'Abnormal number of erythroid precursors', 'XPO:0102531', 'abnormal secondary spermatogonium morphology', 0.4090909090909091, 5.43643956286526, 1.491307481034791, 'HP:0025461', 'Abnormal cell morphology'),
(110748, 'HP:0012131', 'Abnormal number of erythroid precursors', 'XPO:0102929', 'abnormal barrier cell morphology', 0.42857142857142855, 5.43643956286526, 1.526401870347189, 'HP:0025461', 'Abnormal cell morphology'),
(110749, 'HP:0012131', 'Abnormal number of erythroid precursors', 'XPO:0102608', 'abnormal multiciliated cell morphology', 0.4090909090909091, 5.43643956286526, 1.491307481034791, 'HP:0025461', 'Abnormal cell morphology'),
(110750, 'HP:0012131', 'Abnormal number of erythroid precursors', 'XPO:0102181', 'abnormal mitotic cell morphology', 0.42857142857142855, 5.43643956286526, 1.526401870347189, 'HP:0025461', 'Abnormal cell morphology'),
(110751, 'HP:0012131', 'Abnormal number of erythroid precursors', 'XPO:0102147', 'abnormal somatic stem cell morphology', 0.4090909090909091, 5.43643956286526, 1.491307481034791, 'HP:0025461', 'Abnormal cell morphology'),
(110752, 'HP:0012131', 'Abnormal number of erythroid precursors', 'XPO:0103005', 'abnormal oxygen accumulating cell morphology', 0.42857142857142855, 5.43643956286526, 1.526401870347189, 'HP:0025461', 'Abnormal cell morphology'),
(110753, 'HP:0012131', 'Abnormal number of erythroid precursors', 'XPO:0101658', 'abnormal germ cell morphology', 0.42857142857142855, 5.43643956286526, 1.526401870347189, 'HP:0025461', 'Abnormal cell morphology'),
(110754, 'HP:0025083', 'Elevated dermal desmosine content', 'XPO:0101373', 'abnormal oxygen accumulating cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(110755, 'HP:0025083', 'Elevated dermal desmosine content', 'XPO:0100929', 'abnormal dermis', 0.46875, 6.8660902472206855, 1.7940122082596586, 'HP:0000951', 'Abnormality of the skin'),
(110756, 'HP:0025083', 'Elevated dermal desmosine content', 'XPO:0100544', 'abnormal neuromast support cell', 0.4411764705882353, 6.8660902472206855, 1.740447489012273, 'HP:0000951', 'Abnormality of the skin'),
(110757, 'HP:0025083', 'Elevated dermal desmosine content', 'XPO:0100481', 'abnormal anatomical line', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(110758, 'HP:0025083', 'Elevated dermal desmosine content', 'XPO:0100791', 'abnormal multiciliated cell precursor', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(110759, 'HP:0025083', 'Elevated dermal desmosine content', 'XPO:0101278', 'abnormal pigment cell', 0.4411764705882353, 6.8660902472206855, 1.740447489012273, 'HP:0000951', 'Abnormality of the skin'),
(110760, 'HP:0025083', 'Elevated dermal desmosine content', 'XPO:0100653', 'abnormal myoblast', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(110761, 'HP:0025083', 'Elevated dermal desmosine content', 'XPO:0101322', 'abnormal iridophore', 0.42857142857142855, 6.8660902472206855, 1.7154037734456928, 'HP:0000951', 'Abnormality of the skin'),
(110762, 'HP:0025083', 'Elevated dermal desmosine content', 'XPO:0100026', 'abnormal germ cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(110763, 'HP:0025083', 'Elevated dermal desmosine content', 'XPO:0102615', 'abnormal skin gland morphology', 0.46153846153846156, 7.420886955069779, 1.8506822386605823, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(110764, 'HP:0025083', 'Elevated dermal desmosine content', 'XPO:0101515', 'abnormal neuromast mantle cell', 0.4411764705882353, 6.8660902472206855, 1.740447489012273, 'HP:0000951', 'Abnormality of the skin'),
(110765, 'HP:0025083', 'Elevated dermal desmosine content', 'XPO:0100754', 'abnormal electrically active cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(110766, 'HP:0025083', 'Elevated dermal desmosine content', 'XPO:0100081', 'abnormal anatomical entity in vitro', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(110767, 'HP:0025083', 'Elevated dermal desmosine content', 'XPO:0100004', 'abnormal cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(110768, 'HP:0025083', 'Elevated dermal desmosine content', 'XPO:0102840', 'abnormal stratum spongiosum morphology', 0.42857142857142855, 7.420886955069779, 1.7833620281931915, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(110769, 'HP:0025083', 'Elevated dermal desmosine content', 'XPO:0102139', 'abnormal skin morphology', 0.46153846153846156, 7.420886955069779, 1.8506822386605823, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(110770, 'HP:0025083', 'Elevated dermal desmosine content', 'XPO:0101004', 'abnormal acid secreting cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(110771, 'HP:0025083', 'Elevated dermal desmosine content', 'XPO:0103147', 'abnormal neuromast mantle cell morphology', 0.42857142857142855, 7.420886955069779, 1.7833620281931915, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(110772, 'HP:0025083', 'Elevated dermal desmosine content', 'XPO:0100108', 'abnormal cell part', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(110773, 'HP:0025083', 'Elevated dermal desmosine content', 'XPO:0101435', 'abnormal paracrine cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(110774, 'HP:0025083', 'Elevated dermal desmosine content', 'XPO:0101297', 'abnormal barrier cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(110775, 'HP:0025083', 'Elevated dermal desmosine content', 'XPO:0101448', 'abnormal myelin accumulating cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(110776, 'HP:0025083', 'Elevated dermal desmosine content', 'XPO:0101132', 'abnormal apoptotic cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(110777, 'HP:0025083', 'Elevated dermal desmosine content', 'XPO:0100802', 'abnormal exocrine cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(110778, 'HP:0025083', 'Elevated dermal desmosine content', 'XPO:0101095', 'abnormal skin seromucous gland', 0.46875, 6.8660902472206855, 1.7940122082596586, 'HP:0000951', 'Abnormality of the skin'),
(110779, 'HP:0025083', 'Elevated dermal desmosine content', 'XPO:0100852', 'abnormal interdigital region', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(110780, 'HP:0025083', 'Elevated dermal desmosine content', 'XPO:0100549', 'abnormal mitotic cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(110781, 'HP:0025083', 'Elevated dermal desmosine content', 'XPO:0101529', 'abnormal skin mucous gland', 0.4411764705882353, 6.8660902472206855, 1.740447489012273, 'HP:0000951', 'Abnormality of the skin'),
(110782, 'HP:0025083', 'Elevated dermal desmosine content', 'XPO:0103019', 'abnormal melanophore morphology', 0.4090909090909091, 7.420886955069779, 1.7423597190908553, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(110783, 'HP:0025083', 'Elevated dermal desmosine content', 'XPO:0100477', 'abnormal pericyte', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(110784, 'HP:0025083', 'Elevated dermal desmosine content', 'XPO:0102561', 'abnormal dermis morphology', 0.45, 7.420886955069779, 1.8274022900777487, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(110785, 'HP:0025083', 'Elevated dermal desmosine content', 'XPO:0100994', 'abnormal granular gland', 0.46875, 6.8660902472206855, 1.7940122082596586, 'HP:0000951', 'Abnormality of the skin'),
(110786, 'HP:0025083', 'Elevated dermal desmosine content', 'XPO:0102626', 'abnormal granular gland morphology', 0.43902439024390244, 7.420886955069779, 1.8049793268950312, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(110787, 'HP:0025083', 'Elevated dermal desmosine content', 'XPO:0100344', 'abnormal portion of organism substance', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(110788, 'HP:0025083', 'Elevated dermal desmosine content', 'XPO:0102727', 'abnormal skin seromucous gland morphology', 0.43902439024390244, 7.420886955069779, 1.8049793268950312, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(110789, 'HP:0025083', 'Elevated dermal desmosine content', 'XPO:0100172', 'abnormal stem cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(110790, 'HP:0025083', 'Elevated dermal desmosine content', 'XPO:0101014', 'abnormal goblet cell', 0.40540540540540543, 6.8660902472206855, 1.6683974647021622, 'HP:0000951', 'Abnormality of the skin'),
(110791, 'HP:0025083', 'Elevated dermal desmosine content', 'XPO:0101467', 'abnormal alkali secreting cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(110792, 'HP:0025083', 'Elevated dermal desmosine content', 'XPO:0101333', 'abnormal barrier epithelial cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(110793, 'HP:0025083', 'Elevated dermal desmosine content', 'XPO:0100006', 'abnormal anatomical structure', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(110794, 'HP:0025083', 'Elevated dermal desmosine content', 'XPO:0102176', 'abnormal neuromast support cell morphology', 0.42857142857142855, 7.420886955069779, 1.7833620281931915, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(110795, 'HP:0025083', 'Elevated dermal desmosine content', 'XPO:0101254', 'abnormal stratum compactum', 0.4411764705882353, 6.8660902472206855, 1.740447489012273, 'HP:0000951', 'Abnormality of the skin'),
(110796, 'HP:0025083', 'Elevated dermal desmosine content', 'XPO:0100285', 'abnormal progenitor cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(110797, 'HP:0025083', 'Elevated dermal desmosine content', 'XPO:0101237', 'abnormal mucus secreting cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(110798, 'HP:0025083', 'Elevated dermal desmosine content', 'XPO:0102954', 'abnormal iridophore morphology', 0.4090909090909091, 7.420886955069779, 1.7423597190908553, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(110799, 'HP:0025083', 'Elevated dermal desmosine content', 'XPO:0100704', 'abnormal Merkel cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(110800, 'HP:0025083', 'Elevated dermal desmosine content', 'XPO:0100983', 'abnormal skin gland', 0.4838709677419355, 6.8660902472206855, 1.8227182263109507, 'HP:0000951', 'Abnormality of the skin'),
(110801, 'HP:0025083', 'Elevated dermal desmosine content', 'XPO:0101208', 'abnormal stratum spongiosum', 0.4411764705882353, 6.8660902472206855, 1.740447489012273, 'HP:0000951', 'Abnormality of the skin'),
(110802, 'HP:0025083', 'Elevated dermal desmosine content', 'XPO:0100507', 'abnormal skin', 0.5, 6.8660902472206855, 1.8528478414619864, 'HP:0000951', 'Abnormality of the skin'),
(110803, 'HP:0025083', 'Elevated dermal desmosine content', 'XPO:0100533', 'abnormal melanoblast', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(110804, 'HP:0025083', 'Elevated dermal desmosine content', 'XPO:0100715', 'abnormal ciliated cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(110805, 'HP:0025083', 'Elevated dermal desmosine content', 'XPO:0101313', 'abnormal Eberth-Kastschenko layer', 0.4411764705882353, 6.8660902472206855, 1.740447489012273, 'HP:0000951', 'Abnormality of the skin'),
(110806, 'HP:0025083', 'Elevated dermal desmosine content', 'XPO:0100691', 'abnormal keratin accumulating cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(110807, 'HP:0025083', 'Elevated dermal desmosine content', 'XPO:0101241', 'abnormal nucleate erythrocyte', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(110808, 'HP:0025083', 'Elevated dermal desmosine content', 'XPO:0101591', 'abnormal xanthophore', 0.42857142857142855, 6.8660902472206855, 1.7154037734456928, 'HP:0000951', 'Abnormality of the skin'),
(110809, 'HP:0025083', 'Elevated dermal desmosine content', 'XPO:0100289', 'abnormal chondroblast', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(110810, 'HP:0025083', 'Elevated dermal desmosine content', 'XPO:0102886', 'abnormal stratum compactum morphology', 0.42857142857142855, 7.420886955069779, 1.7833620281931915, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(110811, 'HP:0025083', 'Elevated dermal desmosine content', 'XPO:0102910', 'abnormal pigment cell morphology', 0.42857142857142855, 7.420886955069779, 1.7833620281931915, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(110812, 'HP:0025083', 'Elevated dermal desmosine content', 'XPO:0101326', 'abnormal cementoblast', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(110813, 'HP:0025083', 'Elevated dermal desmosine content', 'XPO:0103223', 'abnormal xanthophore morphology', 0.4090909090909091, 7.420886955069779, 1.7423597190908553, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(110814, 'HP:0025083', 'Elevated dermal desmosine content', 'XPO:0101387', 'abnormal melanophore', 0.42857142857142855, 6.8660902472206855, 1.7154037734456928, 'HP:0000951', 'Abnormality of the skin'),
(110815, 'HP:0025083', 'Elevated dermal desmosine content', 'XPO:0102945', 'abnormal Eberth-Kastschenko layer morphology', 0.42857142857142855, 7.420886955069779, 1.7833620281931915, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(110816, 'HP:0025083', 'Elevated dermal desmosine content', 'XPO:0100337', 'abnormal zygote', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(110817, 'HP:0025083', 'Elevated dermal desmosine content', 'XPO:0100638', 'abnormal polar body', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(110818, 'HP:0025083', 'Elevated dermal desmosine content', 'XPO:0101535', 'abnormal absorptive cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(110819, 'HP:0025338', 'Circumlimbal hyperemia', 'XPO:0126243', 'absent optic choroid vascular plexus', 0.4567901234567901, 9.463856994035337, 2.079181667070679, 'UPHENO:0005090', 'abnormal vasculature of eye'),
(110820, 'HP:0025338', 'Circumlimbal hyperemia', 'XPO:0100710', 'abnormal hyaloid vein', 0.5606060606060606, 9.463856994035337, 2.30336614274962, 'UPHENO:0005090', 'abnormal vasculature of eye'),
(110821, 'HP:0025338', 'Circumlimbal hyperemia', 'XPO:0102947', 'abnormal hyaloid vascular plexus morphology', 0.44047619047619047, 9.463856994035337, 2.041715865624827, 'UPHENO:0005090', 'abnormal vasculature of eye'),
(110822, 'HP:0025338', 'Circumlimbal hyperemia', 'XPO:0128178', 'decreased size of the conjunctiva', 0.4235294117647059, 12.720196747295123, 2.3210724775226708, 'HP:0000502', 'Abnormal conjunctiva morphology'),
(110823, 'HP:0025338', 'Circumlimbal hyperemia', 'XPO:0128564', 'decreased size of the hyaloid blood vessel', 0.43529411764705883, 9.463856994035337, 2.029670239166096, 'HP:0008047', 'Abnormality of the vasculature of the eye'),
(110824, 'HP:0025338', 'Circumlimbal hyperemia', 'XPO:0127783', 'abnormally localised hyaloid vascular plexus', 0.47435897435897434, 9.463856994035337, 2.1187886862947445, 'HP:0008047', 'Abnormality of the vasculature of the eye'),
(110825, 'HP:0025338', 'Circumlimbal hyperemia', 'XPO:0101359', 'abnormal hyaloid artery', 0.4625, 9.463856994035337, 2.0921361953136186, 'HP:0008047', 'Abnormality of the vasculature of the eye'),
(110826, 'HP:0025338', 'Circumlimbal hyperemia', 'XPO:0125589', 'absent hyaloid blood vessel', 0.4868421052631579, 9.463856994035337, 2.1464864460055706, 'UPHENO:0005090', 'abnormal vasculature of eye'),
(110827, 'HP:0025338', 'Circumlimbal hyperemia', 'XPO:0125990', 'absent hyaloid vein', 0.4625, 9.463856994035337, 2.0921361953136186, 'HP:0008047', 'Abnormality of the vasculature of the eye'),
(110828, 'HP:0025338', 'Circumlimbal hyperemia', 'XPO:0100371', 'abnormal hyaloid blood vessel', 0.578125, 9.463856994035337, 2.339079375454514, 'HP:0008047', 'Abnormality of the vasculature of the eye'),
(110829, 'HP:0025338', 'Circumlimbal hyperemia', 'XPO:0127645', 'abnormally localised hyaloid vein', 0.4805194805194805, 9.463856994035337, 2.1325026720931706, 'HP:0008047', 'Abnormality of the vasculature of the eye'),
(110830, 'HP:0025338', 'Circumlimbal hyperemia', 'XPO:0127230', 'abnormally localised hyaloid blood vessel', 0.5068493150684932, 9.463856994035337, 2.1901482678880395, 'HP:0008047', 'Abnormality of the vasculature of the eye'),
(110831, 'HP:0025338', 'Circumlimbal hyperemia', 'XPO:0102342', 'abnormal hyaloid vein morphology', 0.43529411764705883, 9.463856994035337, 2.029670239166096, 'UPHENO:0005090', 'abnormal vasculature of eye'),
(110832, 'HP:0025338', 'Circumlimbal hyperemia', 'XPO:0127907', 'abnormally localised optic choroid vascular plexus', 0.4868421052631579, 9.463856994035337, 2.1464864460055706, 'UPHENO:0005090', 'abnormal vasculature of eye'),
(110833, 'HP:0025338', 'Circumlimbal hyperemia', 'XPO:0101315', 'abnormal hyaloid vascular plexus', 0.5606060606060606, 9.463856994035337, 2.30336614274962, 'UPHENO:0005090', 'abnormal vasculature of eye'),
(110834, 'HP:0025338', 'Circumlimbal hyperemia', 'XPO:0127563', 'abnormally localised retinal blood vessel', 0.42045454545454547, 9.463856994035337, 1.994773593838145, 'UPHENO:0005090', 'abnormal vasculature of eye'),
(110835, 'HP:0025338', 'Circumlimbal hyperemia', 'XPO:0102003', 'abnormal hyaloid blood vessel morphology', 0.4805194805194805, 9.463856994035337, 2.1325026720931706, 'UPHENO:0005090', 'abnormal vasculature of eye'),
(110836, 'HP:0025338', 'Circumlimbal hyperemia', 'XPO:0129658', 'increased size of the conjunctiva', 0.4235294117647059, 12.720196747295123, 2.3210724775226708, 'HP:0000502', 'Abnormal conjunctiva morphology'),
(110837, 'HP:0025338', 'Circumlimbal hyperemia', 'XPO:0100329', 'abnormal retinal blood vessel', 0.47435897435897434, 9.463856994035337, 2.1187886862947445, 'UPHENO:0005090', 'abnormal vasculature of eye'),
(110838, 'HP:0025338', 'Circumlimbal hyperemia', 'XPO:0100779', 'abnormal optic choroid vascular plexus', 0.5692307692307692, 9.463856994035337, 2.321016716140737, 'UPHENO:0005090', 'abnormal vasculature of eye'),
(110839, 'HP:0025338', 'Circumlimbal hyperemia', 'XPO:0140968', 'abnormally necrotic conjunctiva', 0.43373493975903615, 12.720196747295123, 2.348870743551279, 'HP:0000502', 'Abnormal conjunctiva morphology'),
(110840, 'HP:0025338', 'Circumlimbal hyperemia', 'XPO:0139722', 'abnormally necrotic hyaloid blood vessel', 0.4457831325301205, 9.463856994035337, 2.0539785336312946, 'HP:0008047', 'Abnormality of the vasculature of the eye'),
(110841, 'HP:0025338', 'Circumlimbal hyperemia', 'XPO:0126122', 'absent hyaloid vascular plexus', 0.4567901234567901, 9.463856994035337, 2.079181667070679, 'UPHENO:0005090', 'abnormal vasculature of eye'),
(110842, 'HP:0025338', 'Circumlimbal hyperemia', 'XPO:0102657', 'abnormal conjunctiva morphology', 0.46153846153846156, 12.720196747295123, 2.422985769090098, 'HP:0000502', 'Abnormal conjunctiva morphology'),
(110843, 'HP:0025338', 'Circumlimbal hyperemia', 'XPO:0127566', 'abnormally localised hyaloid artery', 0.40217391304347827, 9.463856994035337, 1.9509270616235455, 'UPHENO:0005090', 'abnormal vasculature of eye'),
(110844, 'HP:0025338', 'Circumlimbal hyperemia', 'XPO:0130044', 'increased size of the hyaloid blood vessel', 0.43529411764705883, 9.463856994035337, 2.029670239166096, 'HP:0008047', 'Abnormality of the vasculature of the eye'),
(110845, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100386', 'abnormal limb', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(110846, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100856', 'abnormal simple organ', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(110847, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0141771', 'abnormal urea homeostasis', 0.5714285714285714, 1.4755025719078136, 0.918228907628411, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(110848, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0101547', 'abnormal lampbrush chromosome', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(110849, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0107288', 'abnormal larval alimentary system', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(110850, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100501', 'abnormal urogenital system', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(110851, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0101497', 'abnormal ciliary axoneme', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(110852, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100010', 'abnormal multicellular anatomical structure', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(110853, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0133397', 'abnormal insulin receptor signaling pathway', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(110854, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0101326', 'abnormal cementoblast', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(110855, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0131691', 'abnormal molecular function', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(110856, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0141315', 'abnormal anatomical region', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(110857, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0131480', 'absent mating behavior', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(110858, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0101409', 'abnormal perivitelline space', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(110859, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0132054', 'abnormal development of portion of organism substance', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(110860, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0101283', 'abnormal left-ventral blastomere', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(110861, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100688', 'abnormal adipose tissue', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(110862, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0131705', 'abnormal chemotaxis', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(110863, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100786', 'abnormal presumptive axial mesoderm', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(110864, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0128000', 'absent behavior', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(110865, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0141871', 'abnormal cadaverine transport', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(110866, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0107269', 'abnormal right side', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(110867, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0101023', 'abnormal ultimobranchial body', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(110868, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0131723', 'abnormal pathway-restricted SMAD protein phosphorylation', 0.5714285714285714, 1.4755025719078136, 0.918228907628411, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(110869, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0101071', 'abnormal endoplasmic reticulum', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(110870, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100363', 'abnormal cardiovascular system', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(110871, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0131722', 'abnormal determination of left/right symmetry', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(110872, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0141860', 'abnormal malate-aspartate shuttle', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(110873, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100969', 'abnormal disaggregated/reaggregated ectoderm treated with activin', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(110874, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100610', 'abnormal appendage', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(110875, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0101366', 'abnormal morula cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(110876, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0103624', 'absent anterior/posterior pattern specification in midgut', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(110877, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100003', 'abnormal organism subdivision', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(110878, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0116494', 'absent biological process', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(110879, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0101074', 'abnormal germinal vesicle', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(110880, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0141959', 'absent cilium motility in floor plate', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(110881, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0141743', 'abnormal chemical homeostasis within a tissue', 0.5714285714285714, 1.4755025719078136, 0.918228907628411, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(110882, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0141962', 'absent cilium motility in pronephric kidney', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(110883, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100587', 'abnormal vestibuloauditory system', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(110884, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100402', 'abnormal zeugopod', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(110885, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100533', 'abnormal melanoblast', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(110886, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0101241', 'abnormal nucleate erythrocyte', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(110887, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0141714', 'abnormal anterior notochord', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(110888, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0141809', 'abnormal catalytic activity', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(110889, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100081', 'abnormal anatomical entity in vitro', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(110890, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0142057', 'abnormal desmosome', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(110891, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100989', 'abnormal right blastomere', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(110892, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0133403', 'abnormal developmental process', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(110893, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100186', 'abnormal uveal tract', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(110894, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0101228', 'abnormal mesenchymal stem cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(110895, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0141898', 'abnormal maltose metabolic process', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(110896, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0131479', 'absent social behavior', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(110897, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0141798', 'abnormal lipid metabolic process', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(110898, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100585', 'abnormal elastica externa', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(110899, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0131474', 'absent behavioral response to pain', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(110900, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100458', 'abnormal autopod', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(110901, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100032', 'abnormal nervous system', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(110902, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0141770', 'abnormal urate homeostasis', 0.5714285714285714, 1.4755025719078136, 0.918228907628411, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(110903, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0141904', 'abnormal glucosamine metabolic process', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(110904, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100546', 'abnormal whole organism', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(110905, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100205', 'abnormal limb segment', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(110906, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100791', 'abnormal multiciliated cell precursor', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(110907, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0115509', 'abnormally semi-viable whole organism', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(110908, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0131669', 'abnormal Roux spot', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(110909, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0141271', 'increased surface breathing', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(110910, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100070', 'abnormal anatomical system', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(110911, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0131730', 'abnormal regulation of protein folding', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(110912, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100642', 'abnormal gustatory system', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(110913, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100295', 'abnormal extracellular matrix', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(110914, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0107263', 'abnormal anatomical side', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(110915, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0131721', 'abnormal nodal signaling pathway', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(110916, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100704', 'abnormal Merkel cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(110917, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0141600', 'absent metamorphosis', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(110918, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0115512', 'abnormally semi-erect whole organism', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(110919, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0101570', 'abnormal forelimb region', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(110920, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0141724', 'abnormal prevention of polyspermy', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(110921, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0101498', 'abnormal stage II oocyte', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(110922, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0107272', 'abnormal axial region', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(110923, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100293', 'abnormal duct', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(110924, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100640', 'abnormal notochordal sheath', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(110925, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0141795', 'abnormal glycosylation', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(110926, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100900', 'abnormal angioblast', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(110927, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0141792', 'abnormal small molecule metabolic process', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(110928, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0133340', 'abnormal cell adhesion', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(110929, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100852', 'abnormal interdigital region', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(110930, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0141266', 'abnormal surface breathing', 0.5714285714285714, 1.4755025719078136, 0.918228907628411, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(110931, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100384', 'abnormal amputated tissue', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(110932, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0101212', 'abnormal glomeral mesenchyme', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(110933, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0141877', 'abnormal 2-deoxyribose 1-phosphate metabolic process', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(110934, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0107261', 'abnormal dorsal-ventral axis', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(110935, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100192', 'abnormal epithelium', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(110936, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100862', 'abnormal blastomere V1', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(110937, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100762', 'abnormal intersomitic region', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(110938, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100282', 'abnormal pelvic girdle primordium', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(110939, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100416', 'abnormal ligament', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(110940, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0101333', 'abnormal barrier epithelial cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(110941, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0141781', 'abnormal secondary metabolic process', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(110942, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100002', 'abnormal head', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(110943, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0131719', 'abnormal activation of meiosis', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(110944, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0141796', 'abnormal demethylation', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(110945, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100258', 'abnormal organ part', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(110946, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0107266', 'abnormal dorsal side', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(110947, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0131714', 'abnormal establishment of tissue polarity', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(110948, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100104', 'abnormal embryonic structure', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(110949, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100069', 'abnormal urinary system', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(110950, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100162', 'abnormal presumptive rhombomere', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(110951, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0141964', 'absent cilium motility in olfactory pit', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(110952, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0101461', 'abnormal sperm entry point', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(110953, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0101297', 'abnormal barrier cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(110954, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100976', 'abnormal multiciliated cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(110955, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0101168', 'abnormal circulating cell', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(110956, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0141788', 'abnormal hormone biosynthetic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(110957, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0141797', 'abnormal hydrogen metabolic process', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(110958, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100691', 'abnormal keratin accumulating cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(110959, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100308', 'abnormal early embryonic cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(110960, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0131729', 'abnormal regulation of growth rate', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(110961, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0101575', 'abnormal vitelline membrane', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(110962, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0131675', 'abnormal spindle microtubule', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(110963, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100742', 'abnormal musculoskeletal system', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(110964, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0141907', 'abnormal putrescine metabolic process', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(110965, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100307', 'abnormal blastomere', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(110966, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0141791', 'abnormal primary metabolic process', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(110967, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100674', 'abnormal secondary oogonium', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(110968, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0141814', 'abnormal lyase activity', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(110969, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0101389', 'abnormal wedge region', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(110970, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0107270', 'abnormal proximal-distal axis', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(110971, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0103783', 'absent hatching behavior', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(110972, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0131725', 'abnormal phosphorylation of RNA polymerase II C-terminal domain', 0.5714285714285714, 1.4755025719078136, 0.918228907628411, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(110973, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0107267', 'abnormal ventral side', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(110974, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100009', 'abnormal multi-tissue structure', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(110975, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100557', 'abnormal prime meridian', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(110976, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100581', 'abnormal immune system', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(110977, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100888', 'abnormal microtubule', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(110978, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0101096', 'abnormal tendon', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(110979, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0131703', 'abnormal cell division', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(110980, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0101040', 'abnormal axial mesoderm', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(110981, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0101472', 'abnormal zygote cortex', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(110982, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100026', 'abnormal germ cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(110983, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0141745', 'abnormal creatinine homeostasis', 0.5714285714285714, 1.4755025719078136, 0.918228907628411, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(110984, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0141499', 'abnormal tadpole', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(110985, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0141794', 'abnormal prosthetic group metabolic process', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(110986, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0101405', 'abnormal ring structure', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(110987, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100028', 'abnormal anatomical cluster', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(110988, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100894', 'abnormal nucleus', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(110989, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0101513', 'abnormal basal body', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(110990, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0131472', 'absent vocalization behavior', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(110991, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100754', 'abnormal electrically active cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(110992, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0107276', 'abnormal dorsal region', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(110993, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100108', 'abnormal cell part', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(110994, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0107312', 'abnormal filopodium', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(110995, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0141961', 'absent cilium motility in mucociliary epithelium', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(110996, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0131765', 'abnormal development of anatomical region', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(110997, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0141816', 'abnormal ligase activity', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(110998, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100025', 'abnormal oocyte', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(110999, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0101157', 'abnormal female organism', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(111000, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0107339', 'abnormal yolk platelet', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(111001, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0101302', 'abnormal subcortical cytoplasm', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(111002, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0131760', 'abnormal development of anatomical structure', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(111003, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100417', 'abnormal dense regular connective tissue', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(111004, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100547', 'abnormal blastomere V2', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(111005, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0141776', 'abnormal metabolic process', 0.5555555555555556, 1.8210412618256888, 1.005827813247954, 'HP:0000118', 'Phenotypic abnormality'),
(111006, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100268', 'abnormal circulatory system', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(111007, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100665', 'abnormal egg jelly', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(111008, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100493', 'abnormal liver and biliary system', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(111009, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0107253', 'abnormal enteric nervous system', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(111010, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100023', 'abnormal mesenchyme', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(111011, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0107259', 'abnormal animal-vegetal axis', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(111012, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100437', 'abnormal proepicardium', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(111013, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100781', 'abnormal presumptive ectoderm', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(111014, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100265', 'abnormal sensory epithelial cell', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(111015, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100511', 'abnormal stylopod', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(111016, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100653', 'abnormal myoblast', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(111017, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:00000000', 'Xenopus phenotype', 0.6153846153846154, 1.4755025719078136, 0.9528911704452407, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(111018, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0131694', 'abnormal RNA polymerase II activity', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(111019, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100225', 'abnormal endocrine system', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(111020, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100807', 'abnormal matrix-based tissue', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(111021, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0131666', 'abnormal adherens junction', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(111022, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100218', 'abnormal epithelial cell', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(111023, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100120', 'abnormal genital system', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(111024, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100232', 'abnormal lymphatic system', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(111025, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0131728', 'abnormal regulation of cell size', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(111026, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0101004', 'abnormal acid secreting cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(111027, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0141264', 'abnormal schooling behavior', 0.5714285714285714, 1.4755025719078136, 0.918228907628411, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(111028, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100899', 'abnormal secondary spermatogonium', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(111029, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100728', 'abnormal cell condensation', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(111030, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0107271', 'abnormal apical region', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(111031, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0131715', 'abnormal fibroblast growth factor receptor signaling pathway', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(111032, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0141818', 'abnormal peptidoglycan muralytic activity', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(111033, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100515', 'abnormal somatic stem cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(111034, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100574', 'abnormal gastrula cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(111035, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0101061', 'abnormal plasma membrane', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(111036, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100337', 'abnormal zygote', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(111037, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100273', 'abnormal visual system', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(111038, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100477', 'abnormal pericyte', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(111039, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100599', 'abnormal adult immune system', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(111040, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0141911', 'abnormal ribose phosphate metabolic process', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(111041, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0141744', 'abnormal chemical homeostasis', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(111042, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100429', 'abnormal spermatid', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(111043, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0101362', 'abnormal vegetal cortex', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(111044, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0141783', 'abnormal collagen metabolic process', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(111045, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0101078', 'abnormal mucous gland', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(111046, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100152', 'abnormal alimentary system', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(111047, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0133402', 'absent determination of left/right symmetry in alimentary system', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(111048, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100339', 'abnormal circumblastoporal collar', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(111049, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0141786', 'abnormal pigment metabolic process', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(111050, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100135', 'abnormal surface structure', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(111051, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100422', 'abnormal notochord', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(111052, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0131687', 'abnormal astral microtubule', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(111053, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0107268', 'abnormal left side', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(111054, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0131475', 'absent olfactory behavior', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(111055, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100164', 'abnormal neural nucleus', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(111056, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100465', 'abnormal skeletal system', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(111057, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0101072', 'abnormal mitochondrial cloud', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(111058, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100913', 'abnormal Brachets cleft', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(111059, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100031', 'abnormal central nervous system', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(111060, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100802', 'abnormal exocrine cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(111061, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100917', 'abnormal stage III oocyte', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(111062, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0101448', 'abnormal myelin accumulating cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(111063, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0141968', 'absent cilium motility in ciliated cell', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(111064, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100084', 'abnormal anatomical group', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(111065, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0101411', 'abnormal marginal zone (sensu neural)', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(111066, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100176', 'abnormal stage VI oocyte', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(111067, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100531', 'abnormal proliferative region', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(111068, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100239', 'abnormal acellular anatomical structure', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(111069, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0131740', 'abnormal detection of nodal flow', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(111070, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0101237', 'abnormal mucus secreting cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(111071, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100151', 'abnormal primordium', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(111072, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0107258', 'abnormal anatomical axis', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(111073, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0141813', 'abnormal hydrolase activity', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(111074, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0142052', 'abnormal nasal region', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(111075, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0131744', 'abnormal apical constriction', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(111076, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0101132', 'abnormal apoptotic cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(111077, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100573', 'abnormal extraembryonic structure', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(111078, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100549', 'abnormal mitotic cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(111079, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0107260', 'abnormal anterior-posterior axis', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(111080, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100638', 'abnormal polar body', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(111081, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0131476', 'absent mechanosensory behavior', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(111082, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0142051', 'abnormal cerebrospinal fluid', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(111083, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100344', 'abnormal portion of organism substance', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(111084, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0101463', 'abnormal right-ventral blastomere', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(111085, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0101109', 'abnormal egg cell-free extract', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(111086, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0101264', 'abnormal mitotic spindle', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(111087, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100724', 'abnormal kinetochore', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(111088, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0141272', 'absent surface breathing', 0.5714285714285714, 1.4755025719078136, 0.918228907628411, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(111089, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100503', 'abnormal blastomere D2', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(111090, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100842', 'abnormal left-dorsal blastomere', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(111091, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100062', 'abnormal anatomical space', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(111092, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0131482', 'absent locomotory behavior', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(111093, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0131685', 'abnormal cortical actin cytoskeleton', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(111094, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0141718', 'abnormal posterior notochord', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(111095, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0116429', 'abnormal behavior', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(111096, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100231', 'abnormal compound organ', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(111097, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0131738', 'abnormal Wnt signaling pathway', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(111098, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100014', 'abnormal tissue', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(111099, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100626', 'abnormal primordial germ cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(111100, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0101347', 'abnormal hindlimb region', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(111101, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0101311', 'abnormal bottle cell', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(111102, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0101503', 'abnormal organ cortex', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(111103, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100545', 'abnormal male organism', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(111104, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100912', 'abnormal trabecula', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(111105, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0131975', 'abnormal development of anatomical line', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(111106, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0141960', 'absent cilium motility in brain', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(111107, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100202', 'abnormal embryo', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(111108, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100285', 'abnormal progenitor cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(111109, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0141276', 'decreased surface breathing', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(111110, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0131667', 'abnormal actin cytoskeleton', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(111111, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0141715', 'abnormal septum', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(111112, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0131711', 'abnormal establishment of cell polarity', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(111113, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0141738', 'abnormal carbon dioxide homeostasis', 0.5714285714285714, 1.4755025719078136, 0.918228907628411, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(111114, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0141963', 'absent cilium motility in pronephric nephrostome', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(111115, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100999', 'abnormal serous membrane', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(111116, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0131469', 'abnormal heart process', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(111117, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0107284', 'abnormal migrating myoblast', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(111118, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0101220', 'abnormal centriole', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(111119, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100427', 'abnormal olfactory system', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(111120, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0115391', 'abnormally undifferentiated alimentary system', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(111121, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0133401', 'absent determination of left/right symmetry in lateral plate mesoderm', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(111122, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100551', 'abnormal oocyte cortex', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(111123, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0101406', 'abnormal cleavage furrow', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(111124, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0107285', 'abnormal flexural organ', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(111125, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100006', 'abnormal anatomical structure', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(111126, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100274', 'abnormal sensory system', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(111127, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0107265', 'abnormal posterior side', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(111128, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0141812', 'abnormal transferase activity', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(111129, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100317', 'abnormal respiratory system', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(111130, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0131470', 'abnormal heart contraction', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(111131, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0131477', 'absent visual behavior', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(111132, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0141789', 'abnormal hormone catabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(111133, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0141817', 'abnormal demethylase activity', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(111134, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0141777', 'abnormal catabolic process', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(111135, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0141958', 'absent cilium motility in left-right organizer', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(111136, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0116433', 'abnormal axis specification', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(111137, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0115508', 'abnormally peramorphic growth of whole organism', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(111138, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0101373', 'abnormal oxygen accumulating cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(111139, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0101569', 'abnormal activin-induced ectoderm', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(111140, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100004', 'abnormal cell', 0.5263157894736842, 1.8210412618256888, 0.9790009036675816, 'HP:0000118', 'Phenotypic abnormality'),
(111141, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0115758', 'abnormally decreased mobility of melanoblast', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(111142, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0107278', 'abnormal medial region', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(111143, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0107262', 'abnormal left-right axis', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(111144, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100289', 'abnormal chondroblast', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(111145, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0141775', 'abnormal nitrogen compound metabolic process', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(111146, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0141811', 'abnormal oxidoreductase activity', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(111147, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100902', 'abnormal spermatocyte', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(111148, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0101467', 'abnormal alkali secreting cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(111149, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0141787', 'abnormal hormone metabolic process', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(111150, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0101480', 'abnormal stage V oocyte', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(111151, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100721', 'abnormal centromere', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(111152, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100114', 'abnormal peripheral nervous system', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(111153, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0101110', 'abnormal cell-free extract', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(111154, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100415', 'abnormal secretory epithelial cell', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(111155, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0141267', 'abnormal resting posture', 0.5714285714285714, 1.4755025719078136, 0.918228907628411, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(111156, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100956', 'abnormal centrosome', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(111157, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0141767', 'abnormal temperature homeostasis', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(111158, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0141754', 'abnormal homeostatic process', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(111159, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0101519', 'abnormal hypobranchial placode', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(111160, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100915', 'abnormal dermal system', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(111161, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0141748', 'abnormal gas homeostasis', 0.5714285714285714, 1.4755025719078136, 0.918228907628411, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(111162, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100481', 'abnormal anatomical line', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(111163, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100392', 'abnormal cilium', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(111164, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0141782', 'abnormal methylation', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(111165, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0101221', 'abnormal larval immune system', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(111166, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0141815', 'abnormal isomerase activity', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(111167, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0141778', 'abnormal biosynthetic process', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(111168, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100745', 'abnormal anterior lymph sac', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(111169, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0141263', 'abnormal visually guided collision avoidance behavior', 0.5714285714285714, 1.4755025719078136, 0.918228907628411, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(111170, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100060', 'abnormal regenerating tissue', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(111171, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0101451', 'abnormal dorsal lymph space', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(111172, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100643', 'abnormal thoracic region', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(111173, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100715', 'abnormal ciliated cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(111174, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100172', 'abnormal stem cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(111175, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0101141', 'abnormal Keller explant', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(111176, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0101200', 'abnormal joint region', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(111177, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0101535', 'abnormal absorptive cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(111178, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0142056', 'abnormal main body axis', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(111179, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0141841', 'abnormality of whole organism mass', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(111180, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0131677', 'abnormal actin filament', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(111181, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100823', 'abnormal blood', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(111182, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0107273', 'abnormal basal region', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(111183, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0131481', 'absent feeding behavior', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(111184, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0131745', 'abnormal axis elongation', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(111185, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0101378', 'abnormal blastomere D1', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(111186, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0141892', 'abnormal inositol metabolic process', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(111187, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100277', 'abnormal blastocoel', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(111188, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100377', 'abnormal connective tissue', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(111189, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0101468', 'abnormal stage I oocyte', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(111190, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0141810', 'abnormal cyclase activity', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(111191, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100887', 'abnormal right-dorsal blastomere', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(111192, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100991', 'abnormal iliac process primordium', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(111193, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0133388', 'absent insulin receptor signaling pathway', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(111194, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0107264', 'abnormal anterior side', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(111195, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100907', 'abnormal cytoplasm', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(111196, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100394', 'abnormal marginal zone', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(111197, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0101113', 'abnormal stage IV oocyte', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(111198, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100667', 'abnormal vegetal yolk mass', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(111199, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0101435', 'abnormal paracrine cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(111200, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100251', 'abnormal proteinaceous extracellular matrix', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(111201, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0141790', 'abnormal cellular metabolic process', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(111202, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0101136', 'abnormal ooplasm', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(111203, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0141965', 'absent cilium motility in alimentary system', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(111204, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0131798', 'abnormal development of anatomical space', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(111205, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100372', 'abnormal hematological system', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(111206, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100784', 'abnormal left blastomere', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(111207, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0141880', 'abnormal ethanolamine metabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(111208, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0116434', 'abnormal biological process', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(111209, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0101240', 'abnormal ciliated non-epidermal cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(111210, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0141760', 'abnormal multicellular organismal homeostasis', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(111211, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0100423', 'abnormal process', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(111212, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0115505', 'dead whole organism', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(111213, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0141784', 'abnormal cellular hormone metabolic process', 0.5714285714285714, 1.4755025719078136, 0.918228907628411, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(111214, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0141772', 'abnormal water homeostasis', 0.5714285714285714, 1.4755025719078136, 0.918228907628411, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(111215, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0101176', 'abnormal non-ciliated epithelial cell', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(111216, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0141265', 'abnormal escape behavior', 0.5714285714285714, 1.4755025719078136, 0.918228907628411, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(111217, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0141975', 'abnormal cilium motility', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(111218, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0131700', 'abnormal BMP signaling pathway', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(111219, 'HP:0031058', 'Impairment of activities of daily living', 'XPO:0101174', 'abnormal articular system', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(111220, 'HP:0012588', 'Steroid-resistant nephrotic syndrome', 'XPO:0100778', 'abnormal mesonephric kidney', 0.41304347826086957, 6.880013295263146, 1.685747496500148, 'HP:0000077', 'Abnormality of the kidney'),
(111221, 'HP:0012588', 'Steroid-resistant nephrotic syndrome', 'XPO:0141613', 'metaplastic kidney', 0.46511627906976744, 6.880013295263146, 1.788856110435751, 'HP:0000077', 'Abnormality of the kidney'),
(111222, 'HP:0012588', 'Steroid-resistant nephrotic syndrome', 'XPO:0100147', 'abnormal mesonephric mesenchyme', 0.48717948717948717, 6.880013295263146, 1.83079254667872, 'HP:0000077', 'Abnormality of the kidney'),
(111223, 'HP:0012588', 'Steroid-resistant nephrotic syndrome', 'XPO:0100069', 'abnormal urinary system', 0.42857142857142855, 6.355235291121788, 1.6503551943819923, 'HP:0000079', 'Abnormality of the urinary system'),
(111224, 'HP:0012588', 'Steroid-resistant nephrotic syndrome', 'XPO:0107300', 'abnormal embryonic kidney', 0.4634146341463415, 6.880013295263146, 1.7855808142300187, 'HP:0000077', 'Abnormality of the kidney'),
(111225, 'HP:0012588', 'Steroid-resistant nephrotic syndrome', 'XPO:0127733', 'abnormally localised mesonephric sinus', 0.47619047619047616, 6.880013295263146, 1.8100267421417189, 'HP:0000077', 'Abnormality of the kidney'),
(111226, 'HP:0012588', 'Steroid-resistant nephrotic syndrome', 'XPO:0100085', 'abnormal mesonephric sinus', 0.5277777777777778, 6.880013295263146, 1.9055492982485522, 'HP:0000077', 'Abnormality of the kidney'),
(111227, 'HP:0012588', 'Steroid-resistant nephrotic syndrome', 'XPO:0100566', 'abnormal kidney', 0.475, 6.880013295263146, 1.8077627928602786, 'HP:0000077', 'Abnormality of the kidney'),
(111228, 'HP:0012588', 'Steroid-resistant nephrotic syndrome', 'XPO:0127342', 'abnormally localised mesonephric mesenchyme', 0.40816326530612246, 6.880013295263146, 1.6757591390006326, 'HP:0000077', 'Abnormality of the kidney'),
(111229, 'HP:0012588', 'Steroid-resistant nephrotic syndrome', 'XPO:0100761', 'abnormal ureter', 0.425, 6.828345551150745, 1.703539509151187, 'HP:0010935', 'Abnormality of the upper urinary tract'),
(111230, 'HP:0012588', 'Steroid-resistant nephrotic syndrome', 'XPO:0101717', 'abnormal mesonephric sinus morphology', 0.4444444444444444, 6.880013295263146, 1.7486519627369022, 'HP:0000077', 'Abnormality of the kidney'),
(111231, 'HP:0012588', 'Steroid-resistant nephrotic syndrome', 'XPO:0107301', 'abnormal adult kidney', 0.4634146341463415, 6.880013295263146, 1.7855808142300187, 'HP:0000077', 'Abnormality of the kidney'),
(111232, 'HP:0012588', 'Steroid-resistant nephrotic syndrome', 'XPO:0126072', 'absent mesonephric sinus', 0.43478260869565216, 6.880013295263146, 1.7295404384908961, 'HP:0000077', 'Abnormality of the kidney'),
(111233, 'HP:0012588', 'Steroid-resistant nephrotic syndrome', 'XPO:0100271', 'abnormal mesonephric nephron', 0.40425531914893614, 6.880013295263146, 1.6677175931270638, 'HP:0000077', 'Abnormality of the kidney'),
(111234, 'HP:0031768', 'Parafoveal fixation', 'XPO:0101173', 'abnormal retinal layer', 0.40350877192982454, 6.02624522851634, 1.5593725698198597, 'HP:0000478', 'Abnormality of the eye'),
(111235, 'HP:0030045', 'Serpentine fibula', 'XPO:0140858', 'abnormally necrotic iliac process', 0.4090909090909091, 7.61213700143767, 1.764668820499383, 'UPHENO:0079871', 'abnormal anatomical entity morphology in the skeleton of pelvic complex'),
(111236, 'HP:0030045', 'Serpentine fibula', 'XPO:0102880', 'abnormal digit-joint region morphology', 0.42857142857142855, 5.914846961127896, 1.5921477355798221, 'UPHENO:0084763', 'abnormal anatomical entity morphology in the appendage girdle complex'),
(111237, 'HP:0030045', 'Serpentine fibula', 'XPO:0101809', 'abnormal hindlimb digit morphology', 0.40229885057471265, 7.61213700143767, 1.7499582755299095, 'UPHENO:0079871', 'abnormal anatomical entity morphology in the skeleton of pelvic complex'),
(111238, 'HP:0030045', 'Serpentine fibula', 'XPO:0141208', 'abnormally necrotic digit-joint region', 0.40540540540540543, 5.914846961127896, 1.5485189473128784, 'UPHENO:0084763', 'abnormal anatomical entity morphology in the appendage girdle complex'),
(111239, 'HP:0030045', 'Serpentine fibula', 'XPO:0100178', 'abnormal digit', 0.41935483870967744, 5.802924133159483, 1.5599629206829213, 'UPHENO:0076727', 'abnormal limb bone morphology'),
(111240, 'HP:0030045', 'Serpentine fibula', 'XPO:0102566', 'abnormal claw primordium morphology', 0.4069767441860465, 7.61213700143767, 1.7601030461717968, 'UPHENO:0079871', 'abnormal anatomical entity morphology in the skeleton of pelvic complex'),
(111241, 'HP:0030045', 'Serpentine fibula', 'XPO:0141567', 'abnormal joint region morphology in the femur', 0.4148936170212766, 7.61213700143767, 1.7771401334132233, 'UPHENO:0079871', 'abnormal anatomical entity morphology in the skeleton of pelvic complex'),
(111242, 'HP:0030045', 'Serpentine fibula', 'XPO:0103008', 'abnormal iliac process morphology', 0.42857142857142855, 7.61213700143767, 1.806196121462886, 'UPHENO:0079871', 'abnormal anatomical entity morphology in the skeleton of pelvic complex'),
(111243, 'HP:0030045', 'Serpentine fibula', 'XPO:0101859', 'abnormal hindlimb skeleton morphology', 0.4027777777777778, 7.61213700143767, 1.7509996075325265, 'UPHENO:0079871', 'abnormal anatomical entity morphology in the skeleton of pelvic complex'),
(111244, 'HP:0030045', 'Serpentine fibula', 'XPO:0101810', 'abnormal digit morphology', 0.42857142857142855, 5.914846961127896, 1.5921477355798221, 'UPHENO:0084763', 'abnormal anatomical entity morphology in the appendage girdle complex'),
(111245, 'HP:0007029', 'Cerebral berry aneurysm', 'XPO:0101712', 'abnormal aorta morphology', 0.4225352112676056, 9.08792853179561, 1.9595840890778735, 'UPHENO:0087334', 'abnormal systemic artery morphology'),
(111246, 'HP:0007029', 'Cerebral berry aneurysm', 'XPO:0102417', 'abnormal mesencephalic artery morphology', 0.40229885057471265, 9.01729298920255, 1.9046381821363345, 'UPHENO:0015290', 'abnormal artery morphology in the independent continuant'),
(111247, 'HP:0007029', 'Cerebral berry aneurysm', 'XPO:0130811', 'increased size of the cerebral artery', 0.4946236559139785, 13.404694921567193, 2.5749328551473156, 'UPHENO:0021327', 'abnormal cerebral artery morphology'),
(111248, 'HP:0007029', 'Cerebral berry aneurysm', 'XPO:0102695', 'abnormal metencephalic artery morphology', 0.4166666666666667, 9.01729298920255, 1.9383512097057463, 'UPHENO:0015290', 'abnormal artery morphology in the independent continuant'),
(111249, 'HP:0007029', 'Cerebral berry aneurysm', 'XPO:0102673', 'abnormal anterior cerebral vein morphology', 0.4065934065934066, 11.052178506846408, 2.1198450201316867, 'HP:0100659', 'Abnormal cerebral vascular morphology'),
(111250, 'HP:0007029', 'Cerebral berry aneurysm', 'XPO:0129336', 'decreased size of the cerebral artery', 0.4946236559139785, 13.404694921567193, 2.5749328551473156, 'UPHENO:0021327', 'abnormal cerebral artery morphology'),
(111251, 'HP:0007029', 'Cerebral berry aneurysm', 'XPO:0141032', 'abnormally necrotic cerebral artery', 0.5054945054945055, 13.404694921567193, 2.6030750336251005, 'UPHENO:0021327', 'abnormal cerebral artery morphology'),
(111252, 'HP:0007029', 'Cerebral berry aneurysm', 'XPO:0102225', 'abnormal cerebral artery morphology', 0.5476190476190477, 13.404694921567193, 2.709366395778266, 'UPHENO:0021327', 'abnormal cerebral artery morphology'),
(111253, 'HP:0007029', 'Cerebral berry aneurysm', 'XPO:0102409', 'abnormal posterior cerebral vein morphology', 0.4065934065934066, 11.052178506846408, 2.1198450201316867, 'HP:0100659', 'Abnormal cerebral vascular morphology'),
(111254, 'HP:0007029', 'Cerebral berry aneurysm', 'XPO:0102167', 'abnormal cerebral vein morphology', 0.4157303370786517, 11.052178506846408, 2.143531174511975, 'HP:0100659', 'Abnormal cerebral vascular morphology'),
(111255, 'HP:0007029', 'Cerebral berry aneurysm', 'XPO:0101774', 'abnormal paired dorsal aorta morphology', 0.410958904109589, 9.08792853179561, 1.932554048417014, 'UPHENO:0087334', 'abnormal systemic artery morphology'),
(111256, 'HP:0007029', 'Cerebral berry aneurysm', 'XPO:0102754', 'abnormal middle cerebral vein morphology', 0.4065934065934066, 11.052178506846408, 2.1198450201316867, 'HP:0100659', 'Abnormal cerebral vascular morphology'),
(111257, 'HP:0005476', 'Widely patent sagittal suture', 'XPO:0128477', 'decreased size of the neurocranium', 0.4520547945205479, 8.21064164923199, 1.9265668749424245, 'UPHENO:0088115', 'abnormal neurocranium morphology'),
(111258, 'HP:0005476', 'Widely patent sagittal suture', 'XPO:0102921', 'abnormal orbital region morphology', 0.4189189189189189, 7.024697770424301, 1.7154529418548001, 'HP:0000929', 'Abnormal skull morphology'),
(111259, 'HP:0005476', 'Widely patent sagittal suture', 'XPO:0102351', 'abnormal sphenoid region morphology', 0.5076923076923077, 8.21064164923199, 2.0416854817853713, 'UPHENO:0088115', 'abnormal neurocranium morphology'),
(111260, 'HP:0005476', 'Widely patent sagittal suture', 'XPO:0102401', 'abnormal neurocranium morphology', 0.5076923076923077, 8.21064164923199, 2.0416854817853713, 'UPHENO:0088115', 'abnormal neurocranium morphology'),
(111261, 'HP:0005476', 'Widely patent sagittal suture', 'XPO:0128208', 'decreased size of the olfactory region', 0.4583333333333333, 8.21064164923199, 1.9398996767611452, 'UPHENO:0088115', 'abnormal neurocranium morphology'),
(111262, 'HP:0005476', 'Widely patent sagittal suture', 'XPO:0101764', 'abnormal cranium morphology', 0.40625, 4.638757693672553, 1.3727692133255593, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(111263, 'HP:0005476', 'Widely patent sagittal suture', 'XPO:0128947', 'decreased size of the otic region', 0.4583333333333333, 8.21064164923199, 1.9398996767611452, 'UPHENO:0088115', 'abnormal neurocranium morphology'),
(111264, 'HP:0005476', 'Widely patent sagittal suture', 'XPO:0102564', 'abnormal olfactory region morphology', 0.5076923076923077, 8.21064164923199, 2.0416854817853713, 'UPHENO:0088115', 'abnormal neurocranium morphology'),
(111265, 'HP:0005476', 'Widely patent sagittal suture', 'XPO:0130383', 'increased size of the occipital region', 0.4444444444444444, 7.717194259133599, 1.8519892319261708, 'UPHENO:0087814', 'abnormal cranium morphology'),
(111266, 'HP:0005476', 'Widely patent sagittal suture', 'XPO:0129689', 'increased size of the sphenoid region', 0.4583333333333333, 8.21064164923199, 1.9398996767611452, 'UPHENO:0088115', 'abnormal neurocranium morphology'),
(111267, 'HP:0005476', 'Widely patent sagittal suture', 'XPO:0140672', 'abnormally necrotic olfactory region', 0.4714285714285714, 8.21064164923199, 1.967417358673387, 'UPHENO:0088115', 'abnormal neurocranium morphology'),
(111268, 'HP:0005476', 'Widely patent sagittal suture', 'XPO:0128905', 'decreased size of the occipital region', 0.4444444444444444, 7.717194259133599, 1.8519892319261708, 'UPHENO:0087814', 'abnormal cranium morphology'),
(111269, 'HP:0005476', 'Widely patent sagittal suture', 'XPO:0130425', 'increased size of the otic region', 0.4583333333333333, 8.21064164923199, 1.9398996767611452, 'UPHENO:0088115', 'abnormal neurocranium morphology'),
(111270, 'HP:0005476', 'Widely patent sagittal suture', 'XPO:0141185', 'abnormally necrotic occipital region', 0.45714285714285713, 7.717194259133599, 1.878259894888561, 'UPHENO:0087814', 'abnormal cranium morphology'),
(111271, 'HP:0005476', 'Widely patent sagittal suture', 'XPO:0140926', 'abnormally necrotic neurocranium', 0.4714285714285714, 8.21064164923199, 1.967417358673387, 'UPHENO:0088115', 'abnormal neurocranium morphology'),
(111272, 'HP:0005476', 'Widely patent sagittal suture', 'XPO:0141201', 'abnormally necrotic sphenoid region', 0.4714285714285714, 8.21064164923199, 1.967417358673387, 'UPHENO:0088115', 'abnormal neurocranium morphology'),
(111273, 'HP:0005476', 'Widely patent sagittal suture', 'XPO:0129688', 'increased size of the olfactory region', 0.4583333333333333, 8.21064164923199, 1.9398996767611452, 'UPHENO:0088115', 'abnormal neurocranium morphology'),
(111274, 'HP:0005476', 'Widely patent sagittal suture', 'XPO:0129957', 'increased size of the neurocranium', 0.4520547945205479, 8.21064164923199, 1.9265668749424245, 'UPHENO:0088115', 'abnormal neurocranium morphology'),
(111275, 'HP:0005476', 'Widely patent sagittal suture', 'XPO:0130324', 'increased size of the choana', 0.4155844155844156, 7.717194259133599, 1.7908505426566015, 'UPHENO:0087814', 'abnormal cranium morphology'),
(111276, 'HP:0005476', 'Widely patent sagittal suture', 'XPO:0103152', 'abnormal otic region morphology', 0.5076923076923077, 8.21064164923199, 2.0416854817853713, 'UPHENO:0088115', 'abnormal neurocranium morphology'),
(111277, 'HP:0005476', 'Widely patent sagittal suture', 'XPO:0102052', 'abnormal choana morphology', 0.4507042253521127, 7.717194259133599, 1.8649858070383754, 'UPHENO:0087814', 'abnormal cranium morphology'),
(111278, 'HP:0005476', 'Widely patent sagittal suture', 'XPO:0103381', 'increased size of the head', 0.44285714285714284, 7.024697770424301, 1.7637850163909, 'HP:0000929', 'Abnormal skull morphology'),
(111279, 'HP:0005476', 'Widely patent sagittal suture', 'XPO:0128846', 'decreased size of the choana', 0.4155844155844156, 7.717194259133599, 1.7908505426566015, 'UPHENO:0087814', 'abnormal cranium morphology'),
(111280, 'HP:0005476', 'Widely patent sagittal suture', 'XPO:0128209', 'decreased size of the sphenoid region', 0.4583333333333333, 8.21064164923199, 1.9398996767611452, 'UPHENO:0088115', 'abnormal neurocranium morphology'),
(111281, 'HP:0005476', 'Widely patent sagittal suture', 'XPO:0102828', 'abnormal occipital region morphology', 0.49230769230769234, 7.717194259133599, 1.9491624090373367, 'UPHENO:0087814', 'abnormal cranium morphology'),
(111282, 'HP:0005476', 'Widely patent sagittal suture', 'XPO:0140644', 'abnormally necrotic otic region', 0.4714285714285714, 8.21064164923199, 1.967417358673387, 'UPHENO:0088115', 'abnormal neurocranium morphology'),
(111283, 'HP:0005476', 'Widely patent sagittal suture', 'XPO:0141829', 'increased width of head', 0.4189189189189189, 7.024697770424301, 1.7154529418548001, 'HP:0000929', 'Abnormal skull morphology'),
(111284, 'HP:0040257', 'Abnormal size of nasopharyngeal adenoids', 'XPO:0101992', 'abnormal aortic arch 6 morphology', 0.41904761904761906, 8.872199840740173, 1.9281789903888162, 'HP:0033151', 'Abnormal pharynx morphology'),
(111285, 'HP:0040257', 'Abnormal size of nasopharyngeal adenoids', 'XPO:0101749', 'abnormal aortic arch morphology', 0.43564356435643564, 8.872199840740173, 1.9659900209061718, 'HP:0033151', 'Abnormal pharynx morphology'),
(111286, 'HP:0040257', 'Abnormal size of nasopharyngeal adenoids', 'XPO:0102668', 'abnormal pharynx morphology', 0.45, 8.872199840740173, 1.9981215999866169, 'HP:0033151', 'Abnormal pharynx morphology'),
(111287, 'HP:0040257', 'Abnormal size of nasopharyngeal adenoids', 'XPO:0102348', 'abnormal aortic arch 3 morphology', 0.41904761904761906, 8.872199840740173, 1.9281789903888162, 'HP:0033151', 'Abnormal pharynx morphology'),
(111288, 'HP:0040257', 'Abnormal size of nasopharyngeal adenoids', 'XPO:0100875', 'abnormal oropharynx', 0.4050632911392405, 8.127241455820435, 1.8143999481861484, 'HP:0000600', 'Abnormality of the pharynx'),
(111289, 'HP:0040257', 'Abnormal size of nasopharyngeal adenoids', 'XPO:0125070', 'absent aortic arch 6', 0.4166666666666667, 8.127241455820435, 1.8402039578785412, 'HP:0000600', 'Abnormality of the pharynx'),
(111290, 'HP:0040257', 'Abnormal size of nasopharyngeal adenoids', 'XPO:0126876', 'abnormally localised aortic arch', 0.4444444444444444, 8.127241455820435, 1.900554475330284, 'HP:0000600', 'Abnormality of the pharynx'),
(111291, 'HP:0040257', 'Abnormal size of nasopharyngeal adenoids', 'XPO:0125387', 'absent aortic arch 3', 0.4166666666666667, 8.127241455820435, 1.8402039578785412, 'HP:0000600', 'Abnormality of the pharynx'),
(111292, 'HP:0040257', 'Abnormal size of nasopharyngeal adenoids', 'XPO:0101210', 'abnormal aortic arch 2', 0.5, 8.127241455820435, 2.0158424362807272, 'HP:0000600', 'Abnormality of the pharynx'),
(111293, 'HP:0040257', 'Abnormal size of nasopharyngeal adenoids', 'XPO:0127022', 'abnormally localised aortic arch 3', 0.43478260869565216, 8.127241455820435, 1.8797827644866465, 'HP:0000600', 'Abnormality of the pharynx'),
(111294, 'HP:0040257', 'Abnormal size of nasopharyngeal adenoids', 'XPO:0100360', 'abnormal aortic arch 6', 0.5, 8.127241455820435, 2.0158424362807272, 'HP:0000600', 'Abnormality of the pharynx'),
(111295, 'HP:0040257', 'Abnormal size of nasopharyngeal adenoids', 'XPO:0101329', 'abnormal pharyngeal epithelium', 0.4155844155844156, 8.127241455820435, 1.8378125287228213, 'HP:0000600', 'Abnormality of the pharynx'),
(111296, 'HP:0040257', 'Abnormal size of nasopharyngeal adenoids', 'XPO:0125536', 'absent aortic arch 1', 0.42105263157894735, 8.127241455820435, 1.8498638875470566, 'HP:0000600', 'Abnormality of the pharynx'),
(111297, 'HP:0040257', 'Abnormal size of nasopharyngeal adenoids', 'XPO:0128496', 'decreased size of the aortic arch', 0.4090909090909091, 8.872199840740173, 1.9051341943507856, 'HP:0033151', 'Abnormal pharynx morphology'),
(111298, 'HP:0040257', 'Abnormal size of nasopharyngeal adenoids', 'XPO:0101474', 'abnormal aortic arch 5', 0.5, 8.127241455820435, 2.0158424362807272, 'HP:0000600', 'Abnormality of the pharynx'),
(111299, 'HP:0040257', 'Abnormal size of nasopharyngeal adenoids', 'XPO:0125328', 'absent aortic arch 4', 0.4166666666666667, 8.127241455820435, 1.8402039578785412, 'HP:0000600', 'Abnormality of the pharynx'),
(111300, 'HP:0040257', 'Abnormal size of nasopharyngeal adenoids', 'XPO:0101036', 'abnormal pharynx', 0.42105263157894735, 8.127241455820435, 1.8498638875470566, 'HP:0000600', 'Abnormality of the pharynx'),
(111301, 'HP:0040257', 'Abnormal size of nasopharyngeal adenoids', 'XPO:0101748', 'abnormal aortic arch 1 morphology', 0.41904761904761906, 8.872199840740173, 1.9281789903888162, 'HP:0033151', 'Abnormal pharynx morphology'),
(111302, 'HP:0040257', 'Abnormal size of nasopharyngeal adenoids', 'XPO:0127174', 'abnormally localised aortic arch 1', 0.43478260869565216, 8.127241455820435, 1.8797827644866465, 'HP:0000600', 'Abnormality of the pharynx'),
(111303, 'HP:0040257', 'Abnormal size of nasopharyngeal adenoids', 'XPO:0102961', 'abnormal pharyngeal epithelium morphology', 0.4186046511627907, 8.872199840740173, 1.9271595988344108, 'HP:0033151', 'Abnormal pharynx morphology'),
(111304, 'HP:0040257', 'Abnormal size of nasopharyngeal adenoids', 'XPO:0125250', 'absent aortic arch 5', 0.42105263157894735, 8.127241455820435, 1.8498638875470566, 'HP:0000600', 'Abnormality of the pharynx'),
(111305, 'HP:0040257', 'Abnormal size of nasopharyngeal adenoids', 'XPO:0127194', 'abnormally localised aortic arch 2', 0.43478260869565216, 8.127241455820435, 1.8797827644866465, 'HP:0000600', 'Abnormality of the pharynx'),
(111306, 'HP:0040257', 'Abnormal size of nasopharyngeal adenoids', 'XPO:0102507', 'abnormal oropharynx morphology', 0.41379310344827586, 8.872199840740173, 1.916051958197683, 'HP:0033151', 'Abnormal pharynx morphology'),
(111307, 'HP:0040257', 'Abnormal size of nasopharyngeal adenoids', 'XPO:0125251', 'absent aortic arch', 0.43010752688172044, 8.127241455820435, 1.8696490908546237, 'HP:0000600', 'Abnormality of the pharynx'),
(111308, 'HP:0040257', 'Abnormal size of nasopharyngeal adenoids', 'XPO:0126690', 'abnormally localised aortic arch 6', 0.43478260869565216, 8.127241455820435, 1.8797827644866465, 'HP:0000600', 'Abnormality of the pharynx'),
(111309, 'HP:0040257', 'Abnormal size of nasopharyngeal adenoids', 'XPO:0129899', 'increased size of the pharynx', 0.43023255813953487, 8.872199840740173, 1.953742366282417, 'HP:0033151', 'Abnormal pharynx morphology'),
(111310, 'HP:0040257', 'Abnormal size of nasopharyngeal adenoids', 'XPO:0100262', 'abnormal aortic arch 4', 0.5, 8.127241455820435, 2.0158424362807272, 'HP:0000600', 'Abnormality of the pharynx'),
(111311, 'HP:0040257', 'Abnormal size of nasopharyngeal adenoids', 'XPO:0140279', 'abnormally necrotic aortic arch', 0.4036697247706422, 8.872199840740173, 1.8924688815993043, 'HP:0033151', 'Abnormal pharynx morphology'),
(111312, 'HP:0040257', 'Abnormal size of nasopharyngeal adenoids', 'XPO:0126875', 'abnormally localised aortic arch 5', 0.43478260869565216, 8.127241455820435, 1.8797827644866465, 'HP:0000600', 'Abnormality of the pharynx'),
(111313, 'HP:0040257', 'Abnormal size of nasopharyngeal adenoids', 'XPO:0128419', 'decreased size of the pharynx', 0.42528735632183906, 8.872199840740173, 1.942481509571566, 'HP:0033151', 'Abnormal pharynx morphology'),
(111314, 'HP:0040257', 'Abnormal size of nasopharyngeal adenoids', 'XPO:0103106', 'abnormal aortic arch 5 morphology', 0.42718446601941745, 8.872199840740173, 1.9468091717947476, 'HP:0033151', 'Abnormal pharynx morphology'),
(111315, 'HP:0040257', 'Abnormal size of nasopharyngeal adenoids', 'XPO:0129976', 'increased size of the aortic arch', 0.4090909090909091, 8.872199840740173, 1.9051341943507856, 'HP:0033151', 'Abnormal pharynx morphology'),
(111316, 'HP:0040257', 'Abnormal size of nasopharyngeal adenoids', 'XPO:0100716', 'abnormal aortic arch 3', 0.5, 8.127241455820435, 2.0158424362807272, 'HP:0000600', 'Abnormality of the pharynx'),
(111317, 'HP:0040257', 'Abnormal size of nasopharyngeal adenoids', 'XPO:0140110', 'abnormally necrotic pharynx', 0.4235294117647059, 8.872199840740173, 1.9384626846054074, 'HP:0033151', 'Abnormal pharynx morphology'),
(111318, 'HP:0040257', 'Abnormal size of nasopharyngeal adenoids', 'XPO:0101894', 'abnormal aortic arch 4 morphology', 0.41904761904761906, 8.872199840740173, 1.9281789903888162, 'HP:0033151', 'Abnormal pharynx morphology'),
(111319, 'HP:0040257', 'Abnormal size of nasopharyngeal adenoids', 'XPO:0102842', 'abnormal aortic arch 2 morphology', 0.41904761904761906, 8.872199840740173, 1.9281789903888162, 'HP:0033151', 'Abnormal pharynx morphology'),
(111320, 'HP:0040257', 'Abnormal size of nasopharyngeal adenoids', 'XPO:0126957', 'abnormally localised aortic arch 4', 0.43478260869565216, 8.127241455820435, 1.8797827644866465, 'HP:0000600', 'Abnormality of the pharynx'),
(111321, 'HP:0040257', 'Abnormal size of nasopharyngeal adenoids', 'XPO:0100117', 'abnormal aortic arch', 0.5063291139240507, 8.127241455820435, 2.028560811258162, 'HP:0000600', 'Abnormality of the pharynx'),
(111322, 'HP:0040257', 'Abnormal size of nasopharyngeal adenoids', 'XPO:0101395', 'abnormal m. geniohyoideus', 0.43010752688172044, 8.872199840740173, 1.9534584539992526, 'HP:0033151', 'Abnormal pharynx morphology'),
(111323, 'HP:0040257', 'Abnormal size of nasopharyngeal adenoids', 'XPO:0100116', 'abnormal aortic arch 1', 0.5, 8.127241455820435, 2.0158424362807272, 'HP:0000600', 'Abnormality of the pharynx'),
(111324, 'HP:0040257', 'Abnormal size of nasopharyngeal adenoids', 'XPO:0125557', 'absent aortic arch 2', 0.4166666666666667, 8.127241455820435, 1.8402039578785412, 'HP:0000600', 'Abnormality of the pharynx'),
(111325, 'HP:0012901', 'Myotonia of the jaw', 'XPO:0100004', 'abnormal cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(111326, 'HP:0012901', 'Myotonia of the jaw', 'XPO:0100585', 'abnormal elastica externa', 0.41379310344827586, 3.9037819259951223, 1.270967363209146, 'HP:0033127', 'Abnormality of the musculoskeletal system'),
(111327, 'HP:0012901', 'Myotonia of the jaw', 'XPO:0100100', 'abnormal muscle', 0.45161290322580644, 5.968280811662945, 1.6417529121710048, 'UPHENO:0002816', 'abnormal musculature'),
(111328, 'HP:0012901', 'Myotonia of the jaw', 'XPO:0100377', 'abnormal connective tissue', 0.41379310344827586, 3.9037819259951223, 1.270967363209146, 'HP:0033127', 'Abnormality of the musculoskeletal system'),
(111329, 'HP:0012901', 'Myotonia of the jaw', 'XPO:0100275', 'abnormal skeletal muscle', 0.4375, 5.968280811662945, 1.6158969197020392, 'UPHENO:0002816', 'abnormal musculature'),
(111330, 'HP:0012901', 'Myotonia of the jaw', 'XPO:0100746', 'abnormal smooth muscle', 0.4375, 5.968280811662945, 1.6158969197020392, 'UPHENO:0002816', 'abnormal musculature'),
(111331, 'HP:0009817', 'Aplasia involving bones of the lower limbs', 'XPO:0103632', 'abnormally increased number of digit', 0.421875, 5.802924133159483, 1.564643287997829, 'UPHENO:0076727', 'abnormal limb bone morphology'),
(111332, 'HP:0009817', 'Aplasia involving bones of the lower limbs', 'XPO:0124986', 'absent digit', 0.4090909090909091, 5.802924133159483, 1.5407542013636661, 'UPHENO:0076727', 'abnormal limb bone morphology'),
(111333, 'HP:0009817', 'Aplasia involving bones of the lower limbs', 'XPO:0125443', 'absent digit-joint region', 0.4153846153846154, 5.802924133159483, 1.5525609196287773, 'UPHENO:0076727', 'abnormal limb bone morphology'),
(111334, 'HP:0009817', 'Aplasia involving bones of the lower limbs', 'XPO:0101810', 'abnormal digit morphology', 0.421875, 5.802924133159483, 1.564643287997829, 'UPHENO:0076727', 'abnormal limb bone morphology'),
(111335, 'HP:0009817', 'Aplasia involving bones of the lower limbs', 'XPO:0127078', 'abnormally localised digit-joint region', 0.42857142857142855, 5.802924133159483, 1.5770122021213973, 'UPHENO:0076727', 'abnormal limb bone morphology'),
(111336, 'HP:0009817', 'Aplasia involving bones of the lower limbs', 'XPO:0102880', 'abnormal digit-joint region morphology', 0.421875, 5.802924133159483, 1.564643287997829, 'UPHENO:0076727', 'abnormal limb bone morphology'),
(111337, 'HP:0009817', 'Aplasia involving bones of the lower limbs', 'XPO:0101248', 'abnormal digit-joint region', 0.4642857142857143, 5.802924133159483, 1.6414063409496626, 'UPHENO:0076727', 'abnormal limb bone morphology'),
(111338, 'HP:0009817', 'Aplasia involving bones of the lower limbs', 'XPO:0126603', 'abnormally localised digit', 0.421875, 5.802924133159483, 1.564643287997829, 'UPHENO:0076727', 'abnormal limb bone morphology'),
(111339, 'HP:0009817', 'Aplasia involving bones of the lower limbs', 'XPO:0100178', 'abnormal digit', 0.49056603773584906, 5.802924133159483, 1.6872218287130427, 'UPHENO:0076727', 'abnormal limb bone morphology'),
(111340, 'HP:0008407', 'Hyperconvex thumb nails', 'XPO:0101412', 'abnormal claw of hindlimb digit 4', 0.49382716049382713, 10.47734022339896, 2.274641767850241, 'UPHENO:0003071', 'abnormal nail'),
(111341, 'HP:0008407', 'Hyperconvex thumb nails', 'XPO:0141218', 'abnormally necrotic claw of hindlimb digit 5', 0.4519230769230769, 10.983231153128918, 2.227908350287196, 'UPHENO:0088109', 'abnormal nail morphology'),
(111342, 'HP:0008407', 'Hyperconvex thumb nails', 'XPO:0102880', 'abnormal digit-joint region morphology', 0.4857142857142857, 6.466375519622663, 1.7722333273792887, 'UPHENO:0086700', 'abnormal digit morphology'),
(111343, 'HP:0008407', 'Hyperconvex thumb nails', 'XPO:0127409', 'abnormally localised claw of hindlimb digit 4', 0.4444444444444444, 10.47734022339896, 2.1579146542076177, 'UPHENO:0003071', 'abnormal nail'),
(111344, 'HP:0008407', 'Hyperconvex thumb nails', 'XPO:0115801', 'duplicated claw of hindlimb digit 5', 0.43478260869565216, 10.47734022339896, 2.1343301793586873, 'UPHENO:0003071', 'abnormal nail'),
(111345, 'HP:0008407', 'Hyperconvex thumb nails', 'XPO:0130578', 'increased size of the claw of hindlimb digit 2', 0.44339622641509435, 10.983231153128918, 2.206790258982957, 'UPHENO:0088109', 'abnormal nail morphology'),
(111346, 'HP:0008407', 'Hyperconvex thumb nails', 'XPO:0129758', 'increased size of the claw of hindlimb digit 4', 0.44339622641509435, 10.983231153128918, 2.206790258982957, 'UPHENO:0088109', 'abnormal nail morphology'),
(111347, 'HP:0008407', 'Hyperconvex thumb nails', 'XPO:0141208', 'abnormally necrotic digit-joint region', 0.4594594594594595, 6.466375519622663, 1.723669748213883, 'UPHENO:0086700', 'abnormal digit morphology'),
(111348, 'HP:0008407', 'Hyperconvex thumb nails', 'XPO:0126561', 'abnormally localised claw', 0.45977011494252873, 10.47734022339896, 2.19480475642006, 'UPHENO:0003071', 'abnormal nail'),
(111349, 'HP:0008407', 'Hyperconvex thumb nails', 'XPO:0139922', 'abnormally necrotic claw', 0.47, 10.983231153128918, 2.272029630522144, 'UPHENO:0088109', 'abnormal nail morphology'),
(111350, 'HP:0008407', 'Hyperconvex thumb nails', 'XPO:0129977', 'increased size of the digit-joint region', 0.4473684210526316, 6.466375519622663, 1.7008386772845274, 'UPHENO:0086700', 'abnormal digit morphology'),
(111351, 'HP:0008407', 'Hyperconvex thumb nails', 'XPO:0140979', 'abnormally necrotic claw of hindlimb digit 1', 0.4519230769230769, 10.983231153128918, 2.227908350287196, 'UPHENO:0088109', 'abnormal nail morphology'),
(111352, 'HP:0008407', 'Hyperconvex thumb nails', 'XPO:0103191', 'abnormal claw of hindlimb digit 5 morphology', 0.47959183673469385, 10.983231153128918, 2.2950965125699634, 'UPHENO:0088109', 'abnormal nail morphology'),
(111353, 'HP:0008407', 'Hyperconvex thumb nails', 'XPO:0139962', 'abnormally necrotic digit', 0.44155844155844154, 6.466375519622663, 1.689758177070388, 'UPHENO:0086700', 'abnormal digit morphology'),
(111354, 'HP:0008407', 'Hyperconvex thumb nails', 'XPO:0141535', 'abnormally decreased number of claw in the regenerating hindlimb', 0.4166666666666667, 10.47734022339896, 2.08939187957076, 'UPHENO:0003071', 'abnormal nail'),
(111355, 'HP:0008407', 'Hyperconvex thumb nails', 'XPO:0127709', 'abnormally localised claw of hindlimb digit 5', 0.4444444444444444, 10.47734022339896, 2.1579146542076177, 'UPHENO:0003071', 'abnormal nail'),
(111356, 'HP:0008407', 'Hyperconvex thumb nails', 'XPO:0103044', 'abnormal claw of hindlimb digit 4 morphology', 0.47959183673469385, 10.983231153128918, 2.2950965125699634, 'UPHENO:0088109', 'abnormal nail morphology'),
(111357, 'HP:0008407', 'Hyperconvex thumb nails', 'XPO:0115775', 'duplicated bone element in claw of hindlimb digit 5', 0.40816326530612246, 10.47734022339896, 2.0679616527647937, 'UPHENO:0003071', 'abnormal nail'),
(111358, 'HP:0008407', 'Hyperconvex thumb nails', 'XPO:0115798', 'duplicated claw of hindlimb digit 2', 0.43478260869565216, 10.47734022339896, 2.1343301793586873, 'UPHENO:0003071', 'abnormal nail'),
(111359, 'HP:0008407', 'Hyperconvex thumb nails', 'XPO:0103408', 'abnormally increased number of claw of hindlimb digit 1 in the regenerating hindlimb', 0.42105263157894735, 10.47734022339896, 2.1003598913067463, 'UPHENO:0003071', 'abnormal nail'),
(111360, 'HP:0008407', 'Hyperconvex thumb nails', 'XPO:0130653', 'increased size of the claw of hindlimb digit 1', 0.44339622641509435, 10.983231153128918, 2.206790258982957, 'UPHENO:0088109', 'abnormal nail morphology'),
(111361, 'HP:0008407', 'Hyperconvex thumb nails', 'XPO:0128166', 'decreased size of the claw', 0.46078431372549017, 10.983231153128918, 2.2496445562317025, 'UPHENO:0088109', 'abnormal nail morphology'),
(111362, 'HP:0008407', 'Hyperconvex thumb nails', 'XPO:0100825', 'abnormal claw of hindlimb digit 2', 0.49382716049382713, 10.47734022339896, 2.274641767850241, 'UPHENO:0003071', 'abnormal nail'),
(111363, 'HP:0008407', 'Hyperconvex thumb nails', 'XPO:0130944', 'increased size of the claw of hindlimb digit 5', 0.44339622641509435, 10.983231153128918, 2.206790258982957, 'UPHENO:0088109', 'abnormal nail morphology'),
(111364, 'HP:0008407', 'Hyperconvex thumb nails', 'XPO:0128213', 'decreased size of the digit', 0.43037974683544306, 6.466375519622663, 1.6682317162427132, 'UPHENO:0086700', 'abnormal digit morphology'),
(111365, 'HP:0008407', 'Hyperconvex thumb nails', 'XPO:0129471', 'decreased size of the claw of hindlimb digit 5', 0.44339622641509435, 10.983231153128918, 2.206790258982957, 'UPHENO:0088109', 'abnormal nail morphology'),
(111366, 'HP:0008407', 'Hyperconvex thumb nails', 'XPO:0130083', 'increased size of the claw of hindlimb digit 3', 0.44339622641509435, 10.983231153128918, 2.206790258982957, 'UPHENO:0088109', 'abnormal nail morphology'),
(111367, 'HP:0008407', 'Hyperconvex thumb nails', 'XPO:0103411', 'abnormally increased number of claw of hindlimb digit 4 in the regenerating hindlimb', 0.42105263157894735, 10.47734022339896, 2.1003598913067463, 'UPHENO:0003071', 'abnormal nail'),
(111368, 'HP:0008407', 'Hyperconvex thumb nails', 'XPO:0128278', 'decreased size of the claw of hindlimb digit 4', 0.44339622641509435, 10.983231153128918, 2.206790258982957, 'UPHENO:0088109', 'abnormal nail morphology'),
(111369, 'HP:0008407', 'Hyperconvex thumb nails', 'XPO:0101248', 'abnormal digit-joint region', 0.417910447761194, 6.393467666143939, 1.634593813491575, 'UPHENO:0002905', 'abnormal digit'),
(111370, 'HP:0008407', 'Hyperconvex thumb nails', 'XPO:0101559', 'abnormal claw of hindlimb digit 5', 0.49382716049382713, 10.47734022339896, 2.274641767850241, 'UPHENO:0003071', 'abnormal nail'),
(111371, 'HP:0008407', 'Hyperconvex thumb nails', 'XPO:0115771', 'duplicated bone element in claw of hindlimb digit 1', 0.40816326530612246, 10.47734022339896, 2.0679616527647937, 'UPHENO:0003071', 'abnormal nail'),
(111372, 'HP:0008407', 'Hyperconvex thumb nails', 'XPO:0103777', 'decreased size of the claw in the regenerating hindlimb', 0.43119266055045874, 10.983231153128918, 2.1762097009154107, 'UPHENO:0088109', 'abnormal nail morphology'),
(111373, 'HP:0008407', 'Hyperconvex thumb nails', 'XPO:0101295', 'abnormal claw of hindlimb digit 1', 0.49382716049382713, 10.47734022339896, 2.274641767850241, 'UPHENO:0003071', 'abnormal nail'),
(111374, 'HP:0008407', 'Hyperconvex thumb nails', 'XPO:0141568', 'abnormal digit-joint region morphology in the regenerating forelimb', 0.4473684210526316, 6.466375519622663, 1.7008386772845274, 'UPHENO:0086700', 'abnormal digit morphology'),
(111375, 'HP:0008407', 'Hyperconvex thumb nails', 'XPO:0100237', 'abnormal claw', 0.5063291139240507, 10.47734022339896, 2.303254738754359, 'UPHENO:0003071', 'abnormal nail'),
(111376, 'HP:0008407', 'Hyperconvex thumb nails', 'XPO:0100178', 'abnormal digit', 0.4375, 6.393467666143939, 1.6724658752686028, 'HP:0011297', 'Abnormal digit morphology'),
(111377, 'HP:0008407', 'Hyperconvex thumb nails', 'XPO:0102457', 'abnormal claw of hindlimb digit 2 morphology', 0.47959183673469385, 10.983231153128918, 2.2950965125699634, 'UPHENO:0088109', 'abnormal nail morphology'),
(111378, 'HP:0008407', 'Hyperconvex thumb nails', 'XPO:0101165', 'abnormal claw of hindlimb digit 3', 0.49382716049382713, 10.47734022339896, 2.274641767850241, 'UPHENO:0003071', 'abnormal nail'),
(111379, 'HP:0008407', 'Hyperconvex thumb nails', 'XPO:0115772', 'duplicated bone element in claw of hindlimb digit 2', 0.40816326530612246, 10.47734022339896, 2.0679616527647937, 'UPHENO:0003071', 'abnormal nail'),
(111380, 'HP:0008407', 'Hyperconvex thumb nails', 'XPO:0129693', 'increased size of the digit', 0.43037974683544306, 6.466375519622663, 1.6682317162427132, 'UPHENO:0086700', 'abnormal digit morphology'),
(111381, 'HP:0008407', 'Hyperconvex thumb nails', 'XPO:0103412', 'abnormally increased number of claw of hindlimb digit 5 in the regenerating hindlimb', 0.42105263157894735, 10.47734022339896, 2.1003598913067463, 'UPHENO:0003071', 'abnormal nail'),
(111382, 'HP:0008407', 'Hyperconvex thumb nails', 'XPO:0141569', 'abnormal digit-joint region morphology in the regenerating hindlimb', 0.4473684210526316, 6.466375519622663, 1.7008386772845274, 'UPHENO:0086700', 'abnormal digit morphology'),
(111383, 'HP:0008407', 'Hyperconvex thumb nails', 'XPO:0102927', 'abnormal claw of hindlimb digit 1 morphology', 0.47959183673469385, 10.983231153128918, 2.2950965125699634, 'UPHENO:0088109', 'abnormal nail morphology'),
(111384, 'HP:0008407', 'Hyperconvex thumb nails', 'XPO:0115797', 'duplicated claw of hindlimb digit 1', 0.43478260869565216, 10.47734022339896, 2.1343301793586873, 'UPHENO:0003071', 'abnormal nail'),
(111385, 'HP:0008407', 'Hyperconvex thumb nails', 'XPO:0103888', 'abnormally decreased number of claw', 0.4444444444444444, 10.47734022339896, 2.1579146542076177, 'UPHENO:0003071', 'abnormal nail'),
(111386, 'HP:0008407', 'Hyperconvex thumb nails', 'XPO:0115773', 'duplicated bone element in claw of hindlimb digit 3', 0.40816326530612246, 10.47734022339896, 2.0679616527647937, 'UPHENO:0003071', 'abnormal nail'),
(111387, 'HP:0008407', 'Hyperconvex thumb nails', 'XPO:0129101', 'decreased size of the claw of hindlimb digit 2', 0.44339622641509435, 10.983231153128918, 2.206790258982957, 'UPHENO:0088109', 'abnormal nail morphology'),
(111388, 'HP:0008407', 'Hyperconvex thumb nails', 'XPO:0140536', 'abnormally necrotic claw of hindlimb digit 2', 0.4519230769230769, 10.983231153128918, 2.227908350287196, 'UPHENO:0088109', 'abnormal nail morphology'),
(111389, 'HP:0008407', 'Hyperconvex thumb nails', 'XPO:0140433', 'abnormally necrotic claw of hindlimb digit 4', 0.4519230769230769, 10.983231153128918, 2.227908350287196, 'UPHENO:0088109', 'abnormal nail morphology'),
(111390, 'HP:0008407', 'Hyperconvex thumb nails', 'XPO:0127822', 'abnormally localised claw of hindlimb digit 3', 0.4444444444444444, 10.47734022339896, 2.1579146542076177, 'UPHENO:0003071', 'abnormal nail'),
(111391, 'HP:0008407', 'Hyperconvex thumb nails', 'XPO:0128603', 'decreased size of the claw of hindlimb digit 3', 0.44339622641509435, 10.983231153128918, 2.206790258982957, 'UPHENO:0088109', 'abnormal nail morphology'),
(111392, 'HP:0008407', 'Hyperconvex thumb nails', 'XPO:0127908', 'abnormally localised claw of hindlimb digit 1', 0.4444444444444444, 10.47734022339896, 2.1579146542076177, 'UPHENO:0003071', 'abnormal nail'),
(111393, 'HP:0008407', 'Hyperconvex thumb nails', 'XPO:0101869', 'abnormal claw morphology', 0.49473684210526314, 10.983231153128918, 2.331053216211751, 'UPHENO:0088109', 'abnormal nail morphology'),
(111394, 'HP:0008407', 'Hyperconvex thumb nails', 'XPO:0141558', 'abnormal claw morphology in the regenerating hindlimb', 0.46534653465346537, 10.983231153128918, 2.260753979628594, 'UPHENO:0088109', 'abnormal nail morphology'),
(111395, 'HP:0008407', 'Hyperconvex thumb nails', 'XPO:0141137', 'abnormally necrotic claw of hindlimb digit 3', 0.4519230769230769, 10.983231153128918, 2.227908350287196, 'UPHENO:0088109', 'abnormal nail morphology'),
(111396, 'HP:0008407', 'Hyperconvex thumb nails', 'XPO:0101810', 'abnormal digit morphology', 0.4857142857142857, 6.466375519622663, 1.7722333273792887, 'UPHENO:0086700', 'abnormal digit morphology'),
(111397, 'HP:0008407', 'Hyperconvex thumb nails', 'XPO:0127382', 'abnormally localised claw of hindlimb digit 2', 0.4444444444444444, 10.47734022339896, 2.1579146542076177, 'UPHENO:0003071', 'abnormal nail'),
(111398, 'HP:0008407', 'Hyperconvex thumb nails', 'XPO:0128497', 'decreased size of the digit-joint region', 0.4473684210526316, 6.466375519622663, 1.7008386772845274, 'UPHENO:0086700', 'abnormal digit morphology'),
(111399, 'HP:0008407', 'Hyperconvex thumb nails', 'XPO:0115774', 'duplicated bone element in claw of hindlimb digit 4', 0.40816326530612246, 10.47734022339896, 2.0679616527647937, 'UPHENO:0003071', 'abnormal nail'),
(111400, 'HP:0008407', 'Hyperconvex thumb nails', 'XPO:0115799', 'duplicated claw of hindlimb digit 3', 0.43478260869565216, 10.47734022339896, 2.1343301793586873, 'UPHENO:0003071', 'abnormal nail'),
(111401, 'HP:0008407', 'Hyperconvex thumb nails', 'XPO:0115800', 'duplicated claw of hindlimb digit 4', 0.43478260869565216, 10.47734022339896, 2.1343301793586873, 'UPHENO:0003071', 'abnormal nail'),
(111402, 'HP:0008407', 'Hyperconvex thumb nails', 'XPO:0129646', 'increased size of the claw', 0.46078431372549017, 10.983231153128918, 2.2496445562317025, 'UPHENO:0088109', 'abnormal nail morphology'),
(111403, 'HP:0008407', 'Hyperconvex thumb nails', 'XPO:0102797', 'abnormal claw of hindlimb digit 3 morphology', 0.47959183673469385, 10.983231153128918, 2.2950965125699634, 'UPHENO:0088109', 'abnormal nail morphology'),
(111404, 'HP:0008407', 'Hyperconvex thumb nails', 'XPO:0129177', 'decreased size of the claw of hindlimb digit 1', 0.44339622641509435, 10.983231153128918, 2.206790258982957, 'UPHENO:0088109', 'abnormal nail morphology'),
(111405, 'HP:0008407', 'Hyperconvex thumb nails', 'XPO:0124947', 'absent claw', 0.40869565217391307, 10.983231153128918, 2.118678554926363, 'UPHENO:0088109', 'abnormal nail morphology'),
(111406, 'HP:0008407', 'Hyperconvex thumb nails', 'XPO:0103409', 'abnormally increased number of claw of hindlimb digit 2 in the regenerating hindlimb', 0.42105263157894735, 10.47734022339896, 2.1003598913067463, 'UPHENO:0003071', 'abnormal nail'),
(111407, 'HP:0008407', 'Hyperconvex thumb nails', 'XPO:0103410', 'abnormally increased number of claw of hindlimb digit 3 in the regenerating hindlimb', 0.42105263157894735, 10.47734022339896, 2.1003598913067463, 'UPHENO:0003071', 'abnormal nail'),
(111408, 'HP:0032306', 'Increased circulating mannose-binding protein concentration', 'XPO:0141873', 'abnormal tricarboxylic acid metabolic process', 0.42592592592592593, 7.41682187759612, 1.7773622944247445, 'HP:0430071', 'Abnormal circulating organic compound concentration'),
(111409, 'HP:0025483', 'Abnormal circulating thyroglobulin level', 'XPO:0141869', 'abnormal alpha-amino acid metabolic process', 0.40350877192982454, 7.41682187759612, 1.729957423594889, 'HP:0430071', 'Abnormal circulating organic compound concentration'),
(111410, 'HP:0025483', 'Abnormal circulating thyroglobulin level', 'XPO:0141873', 'abnormal tricarboxylic acid metabolic process', 0.4339622641509434, 7.41682187759612, 1.7940515084037758, 'HP:0430071', 'Abnormal circulating organic compound concentration'),
(111411, 'HP:0003524', 'Decreased methionine synthase activity', 'XPO:0141869', 'abnormal alpha-amino acid metabolic process', 0.5616438356164384, 10.156767408123608, 2.3884065408892545, 'UPHENO:0050249', 'abnormal alpha-amino acid metabolic process'),
(111412, 'HP:0003524', 'Decreased methionine synthase activity', 'XPO:0141848', 'abnormal proline metabolic process', 0.5394736842105263, 10.156767408123608, 2.3407923302441507, 'UPHENO:0050249', 'abnormal alpha-amino acid metabolic process'),
(111413, 'HP:0003524', 'Decreased methionine synthase activity', 'XPO:0141913', 'abnormal L-serine metabolic process', 0.5324675324675324, 10.156767408123608, 2.3255427064774006, 'UPHENO:0050249', 'abnormal alpha-amino acid metabolic process'),
(111414, 'HP:0003524', 'Decreased methionine synthase activity', 'XPO:0141868', 'abnormal asparagine metabolic process', 0.56, 12.511610125483706, 2.64697972607855, 'UPHENO:0050388', 'abnormal aspartate family amino acid metabolic process'),
(111415, 'HP:0003524', 'Decreased methionine synthase activity', 'XPO:0141893', 'abnormal isoleucine metabolic process', 0.5394736842105263, 10.156767408123608, 2.3407923302441507, 'UPHENO:0050249', 'abnormal alpha-amino acid metabolic process'),
(111416, 'HP:0003524', 'Decreased methionine synthase activity', 'XPO:0141873', 'abnormal tricarboxylic acid metabolic process', 0.5068493150684932, 10.86332168939372, 2.346501045735525, 'HP:0012379', 'Abnormal circulating enzyme concentration or activity'),
(111417, 'HP:0003524', 'Decreased methionine synthase activity', 'XPO:0141882', 'abnormal gamma-aminobutyric acid metabolic process', 0.5333333333333333, 10.007478699375595, 2.3102644811796584, 'UPHENO:0051195', 'abnormal amino acid metabolic process'),
(111418, 'HP:0003524', 'Decreased methionine synthase activity', 'XPO:0141847', 'abnormal arginine metabolic process', 0.5394736842105263, 10.156767408123608, 2.3407923302441507, 'UPHENO:0050249', 'abnormal alpha-amino acid metabolic process'),
(111419, 'HP:0003524', 'Decreased methionine synthase activity', 'XPO:0141922', 'abnormal valine metabolic process', 0.5394736842105263, 10.156767408123608, 2.3407923302441507, 'UPHENO:0050249', 'abnormal alpha-amino acid metabolic process'),
(111420, 'HP:0003524', 'Decreased methionine synthase activity', 'XPO:0141857', 'abnormal glycine metabolic process', 0.5324675324675324, 10.156767408123608, 2.3255427064774006, 'UPHENO:0050249', 'abnormal alpha-amino acid metabolic process'),
(111421, 'HP:0003524', 'Decreased methionine synthase activity', 'XPO:0141889', 'abnormal homoserine metabolic process', 0.5324675324675324, 10.156767408123608, 2.3255427064774006, 'UPHENO:0050249', 'abnormal alpha-amino acid metabolic process'),
(111422, 'HP:0003524', 'Decreased methionine synthase activity', 'XPO:0141912', 'abnormal D-serine metabolic process', 0.5324675324675324, 10.156767408123608, 2.3255427064774006, 'UPHENO:0050249', 'abnormal alpha-amino acid metabolic process'),
(111423, 'HP:0003524', 'Decreased methionine synthase activity', 'XPO:0141917', 'abnormal tryptophan metabolic process', 0.5394736842105263, 10.156767408123608, 2.3407923302441507, 'UPHENO:0050249', 'abnormal alpha-amino acid metabolic process'),
(111424, 'HP:0003524', 'Decreased methionine synthase activity', 'XPO:0141858', 'abnormal serine family amino acid metabolic process', 0.5466666666666666, 10.156767408123608, 2.3563459387593264, 'UPHENO:0050249', 'abnormal alpha-amino acid metabolic process'),
(111425, 'HP:0003524', 'Decreased methionine synthase activity', 'XPO:0141843', 'abnormal alanine metabolic process', 0.5466666666666666, 10.156767408123608, 2.3563459387593264, 'UPHENO:0050249', 'abnormal alpha-amino acid metabolic process'),
(111426, 'HP:0003524', 'Decreased methionine synthase activity', 'XPO:0141888', 'abnormal threonine metabolic process', 0.56, 12.511610125483706, 2.64697972607855, 'UPHENO:0050388', 'abnormal aspartate family amino acid metabolic process'),
(111427, 'HP:0003524', 'Decreased methionine synthase activity', 'XPO:0141905', 'abnormal ornithine metabolic process', 0.5466666666666666, 10.156767408123608, 2.3563459387593264, 'UPHENO:0050249', 'abnormal alpha-amino acid metabolic process'),
(111428, 'HP:0003524', 'Decreased methionine synthase activity', 'XPO:0141887', 'abnormal histidine metabolic process', 0.5394736842105263, 10.156767408123608, 2.3407923302441507, 'UPHENO:0050249', 'abnormal alpha-amino acid metabolic process'),
(111429, 'HP:0003524', 'Decreased methionine synthase activity', 'XPO:0141896', 'abnormal lysine metabolic process', 0.56, 12.511610125483706, 2.64697972607855, 'UPHENO:0050388', 'abnormal aspartate family amino acid metabolic process'),
(111430, 'HP:0003524', 'Decreased methionine synthase activity', 'XPO:0141853', 'abnormal glutamate metabolic process', 0.5256410256410257, 10.156767408123608, 2.310587292790176, 'UPHENO:0050249', 'abnormal alpha-amino acid metabolic process'),
(111431, 'HP:0003524', 'Decreased methionine synthase activity', 'XPO:0141918', 'abnormal tyrosine metabolic process', 0.5394736842105263, 10.156767408123608, 2.3407923302441507, 'UPHENO:0050249', 'abnormal alpha-amino acid metabolic process'),
(111432, 'HP:0003524', 'Decreased methionine synthase activity', 'XPO:0141895', 'abnormal leucine metabolic process', 0.5394736842105263, 10.156767408123608, 2.3407923302441507, 'UPHENO:0050249', 'abnormal alpha-amino acid metabolic process'),
(111433, 'HP:0033577', 'In situ pulmonary artery thrombosis', 'XPO:0101548', 'abnormal pulmonary vein', 0.5, 11.341685124041394, 2.381353094780507, 'UPHENO:0002960', 'abnormal lung vasculature'),
(111434, 'HP:0033577', 'In situ pulmonary artery thrombosis', 'XPO:0128233', 'decreased size of the pulmonary vein', 0.47126436781609193, 11.341685124041394, 2.3119109130653244, 'UPHENO:0002960', 'abnormal lung vasculature'),
(111435, 'HP:0033577', 'In situ pulmonary artery thrombosis', 'XPO:0101842', 'abnormal pulmonary artery morphology', 0.647887323943662, 12.627087342903641, 2.860232477928451, 'UPHENO:0076750', 'abnormal pulmonary artery morphology'),
(111436, 'HP:0033577', 'In situ pulmonary artery thrombosis', 'XPO:0125948', 'absent pulmonary artery', 0.5974025974025974, 12.627087342903641, 2.7465350491628713, 'UPHENO:0076750', 'abnormal pulmonary artery morphology'),
(111437, 'HP:0033577', 'In situ pulmonary artery thrombosis', 'XPO:0126220', 'absent pulmonary vein', 0.4230769230769231, 11.341685124041394, 2.190526248367443, 'UPHENO:0002960', 'abnormal lung vasculature'),
(111438, 'HP:0033577', 'In situ pulmonary artery thrombosis', 'XPO:0101949', 'abnormal respiratory system morphology', 0.42105263157894735, 7.241224942262181, 1.746120504946495, 'HP:0012252', 'Abnormal respiratory system morphology'),
(111439, 'HP:0033577', 'In situ pulmonary artery thrombosis', 'XPO:0140939', 'abnormally necrotic pulmonary artery', 0.5897435897435898, 12.627087342903641, 2.72887226113826, 'UPHENO:0076750', 'abnormal pulmonary artery morphology'),
(111440, 'HP:0033577', 'In situ pulmonary artery thrombosis', 'XPO:0128337', 'decreased size of the pulmonary artery', 0.575, 12.627087342903641, 2.694545457432402, 'UPHENO:0076750', 'abnormal pulmonary artery morphology'),
(111441, 'HP:0033577', 'In situ pulmonary artery thrombosis', 'XPO:0127602', 'abnormally localised pulmonary artery', 0.47297297297297297, 12.257853533237922, 2.407827532835938, 'HP:0004414', 'Abnormality of the pulmonary artery'),
(111442, 'HP:0033577', 'In situ pulmonary artery thrombosis', 'XPO:0141016', 'abnormally necrotic pulmonary vein', 0.4823529411764706, 11.341685124041394, 2.338951726196757, 'UPHENO:0002960', 'abnormal lung vasculature'),
(111443, 'HP:0033577', 'In situ pulmonary artery thrombosis', 'XPO:0129817', 'increased size of the pulmonary artery', 0.575, 12.627087342903641, 2.694545457432402, 'UPHENO:0076750', 'abnormal pulmonary artery morphology'),
(111444, 'HP:0033577', 'In situ pulmonary artery thrombosis', 'XPO:0129713', 'increased size of the pulmonary vein', 0.47126436781609193, 11.341685124041394, 2.3119109130653244, 'UPHENO:0002960', 'abnormal lung vasculature'),
(111445, 'HP:0033577', 'In situ pulmonary artery thrombosis', 'XPO:0127882', 'abnormally localised pulmonary vein', 0.4342105263157895, 11.341685124041394, 2.219161793790163, 'UPHENO:0002960', 'abnormal lung vasculature'),
(111446, 'HP:0033577', 'In situ pulmonary artery thrombosis', 'XPO:0100210', 'abnormal pulmonary artery', 0.546875, 12.257853533237922, 2.589114453049438, 'HP:0004414', 'Abnormality of the pulmonary artery'),
(111447, 'HP:0033577', 'In situ pulmonary artery thrombosis', 'XPO:0103180', 'abnormal pulmonary vein morphology', 0.5256410256410257, 11.341685124041394, 2.441650057051313, 'UPHENO:0002960', 'abnormal lung vasculature'),
(111448, 'HP:0033796', 'Abnormal leukocyte physiology', 'XPO:0100242', 'abnormal right lymph heart', 0.40625, 5.64885357140806, 1.5148751642906173, 'HP:0002715', 'Abnormality of the immune system'),
(111449, 'HP:0033796', 'Abnormal leukocyte physiology', 'XPO:0100540', 'abnormal left lymph heart', 0.40625, 5.64885357140806, 1.5148751642906173, 'HP:0002715', 'Abnormality of the immune system'),
(111450, 'HP:0033796', 'Abnormal leukocyte physiology', 'XPO:0100004', 'abnormal cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(111451, 'HP:0033796', 'Abnormal leukocyte physiology', 'XPO:0101451', 'abnormal dorsal lymph space', 0.4482758620689655, 5.64885357140806, 1.5913028324062968, 'HP:0002715', 'Abnormality of the immune system'),
(111452, 'HP:0033796', 'Abnormal leukocyte physiology', 'XPO:0100616', 'abnormal ventral blood island', 0.40625, 5.574066539846944, 1.5048137864243607, 'HP:0001871', 'Abnormality of blood and blood-forming tissues'),
(111453, 'HP:0033796', 'Abnormal leukocyte physiology', 'XPO:0141497', 'abnormal lymphoblast', 0.41935483870967744, 5.64885357140806, 1.5391147060347428, 'HP:0002715', 'Abnormality of the immune system'),
(111454, 'HP:0033796', 'Abnormal leukocyte physiology', 'XPO:0101450', 'abnormal myeloid cell', 0.41935483870967744, 5.574066539846944, 1.5288923359002506, 'UPHENO:0004459', 'abnormal hematopoietic system'),
(111455, 'HP:0033796', 'Abnormal leukocyte physiology', 'XPO:0141628', 'metaplastic thymus', 0.4444444444444444, 5.64885357140806, 1.5844877996666529, 'HP:0002715', 'Abnormality of the immune system'),
(111456, 'HP:0033796', 'Abnormal leukocyte physiology', 'XPO:0101029', 'abnormal right spleen primordium', 0.41935483870967744, 5.64885357140806, 1.5391147060347428, 'HP:0002715', 'Abnormality of the immune system'),
(111457, 'HP:0033796', 'Abnormal leukocyte physiology', 'XPO:0100823', 'abnormal blood', 0.4482758620689655, 5.574066539846944, 1.5807338433081215, 'HP:0001871', 'Abnormality of blood and blood-forming tissues'),
(111458, 'HP:0033796', 'Abnormal leukocyte physiology', 'XPO:0101484', 'abnormal bone marrow', 0.45454545454545453, 5.64885357140806, 1.6023921849149136, 'HP:0002715', 'Abnormality of the immune system'),
(111459, 'HP:0033796', 'Abnormal leukocyte physiology', 'XPO:0101221', 'abnormal larval immune system', 0.4642857142857143, 5.64885357140806, 1.6194696710023933, 'HP:0002715', 'Abnormality of the immune system'),
(111460, 'HP:0033796', 'Abnormal leukocyte physiology', 'XPO:0101202', 'abnormal thymus', 0.4411764705882353, 5.64885357140806, 1.5786517290091426, 'HP:0002715', 'Abnormality of the immune system'),
(111461, 'HP:0033796', 'Abnormal leukocyte physiology', 'XPO:0100449', 'abnormal lymphocyte', 0.41935483870967744, 5.64885357140806, 1.5391147060347428, 'HP:0002715', 'Abnormality of the immune system'),
(111462, 'HP:0033796', 'Abnormal leukocyte physiology', 'XPO:0100599', 'abnormal adult immune system', 0.4642857142857143, 5.64885357140806, 1.6194696710023933, 'HP:0002715', 'Abnormality of the immune system'),
(111463, 'HP:0033796', 'Abnormal leukocyte physiology', 'XPO:0101107', 'abnormal erythroid cell', 0.41935483870967744, 5.574066539846944, 1.5288923359002506, 'UPHENO:0004459', 'abnormal hematopoietic system'),
(111464, 'HP:0033796', 'Abnormal leukocyte physiology', 'XPO:0101587', 'abnormal hemangioblast', 0.41935483870967744, 5.574066539846944, 1.5288923359002506, 'UPHENO:0004459', 'abnormal hematopoietic system'),
(111465, 'HP:0033796', 'Abnormal leukocyte physiology', 'XPO:0101216', 'abnormal macrophage', 0.40540540540540543, 5.64885357140806, 1.5132996306721471, 'HP:0002715', 'Abnormality of the immune system'),
(111466, 'HP:0033796', 'Abnormal leukocyte physiology', 'XPO:0100372', 'abnormal hematological system', 0.48148148148148145, 5.574066539846944, 1.6382337487311942, 'UPHENO:0004459', 'abnormal hematopoietic system'),
(111467, 'HP:0033796', 'Abnormal leukocyte physiology', 'XPO:0100232', 'abnormal lymphatic system', 0.48148148148148145, 5.64885357140806, 1.6491871895674883, 'HP:0002715', 'Abnormality of the immune system'),
(111468, 'HP:0033796', 'Abnormal leukocyte physiology', 'XPO:0100745', 'abnormal anterior lymph sac', 0.43333333333333335, 5.64885357140806, 1.5645563421015427, 'HP:0002715', 'Abnormality of the immune system'),
(111469, 'HP:0033796', 'Abnormal leukocyte physiology', 'XPO:0101083', 'abnormal T cell', 0.40625, 5.64885357140806, 1.5148751642906173, 'HP:0002715', 'Abnormality of the immune system'),
(111470, 'HP:0033796', 'Abnormal leukocyte physiology', 'XPO:0101518', 'abnormal B cell', 0.40625, 5.64885357140806, 1.5148751642906173, 'HP:0002715', 'Abnormality of the immune system'),
(111471, 'HP:0033796', 'Abnormal leukocyte physiology', 'XPO:0107254', 'abnormal neutrophil', 0.40540540540540543, 5.64885357140806, 1.5132996306721471, 'HP:0002715', 'Abnormality of the immune system'),
(111472, 'HP:0033796', 'Abnormal leukocyte physiology', 'XPO:0100581', 'abnormal immune system', 0.48148148148148145, 5.64885357140806, 1.6491871895674883, 'HP:0002715', 'Abnormality of the immune system'),
(111473, 'HP:0010228', 'Absent epiphyses of the phalanges of the hand', 'XPO:0115788', 'duplicated forelimb digit 4 in regenerating forelimb', 0.44029850746268656, 7.774297771301195, 1.8501382935538648, 'HP:0005918', 'Abnormal finger phalanx morphology'),
(111474, 'HP:0010228', 'Absent epiphyses of the phalanges of the hand', 'XPO:0103609', 'abnormally increased number of forelimb digit in the regenerating forelimb', 0.4573643410852713, 7.774297771301195, 1.8856528253026494, 'HP:0005918', 'Abnormal finger phalanx morphology'),
(111475, 'HP:0010228', 'Absent epiphyses of the phalanges of the hand', 'XPO:0102787', 'abnormal forelimb digit 5 morphology', 0.41228070175438597, 7.492661022682715, 1.7575777491876043, 'HP:0001167', 'Abnormal finger morphology'),
(111476, 'HP:0010228', 'Absent epiphyses of the phalanges of the hand', 'XPO:0115786', 'duplicated forelimb digit 2 in regenerating forelimb', 0.44029850746268656, 7.774297771301195, 1.8501382935538648, 'HP:0005918', 'Abnormal finger phalanx morphology'),
(111477, 'HP:0010228', 'Absent epiphyses of the phalanges of the hand', 'XPO:0115787', 'duplicated forelimb digit 3 in regenerating forelimb', 0.44029850746268656, 7.774297771301195, 1.8501382935538648, 'HP:0005918', 'Abnormal finger phalanx morphology'),
(111478, 'HP:0010228', 'Absent epiphyses of the phalanges of the hand', 'XPO:0125257', 'absent forelimb digit', 0.432, 10.497804325958676, 2.1295660282823228, 'UPHENO:0026181', 'absent anatomical entity in the forelimb'),
(111479, 'HP:0010228', 'Absent epiphyses of the phalanges of the hand', 'XPO:0102214', 'abnormal forelimb digit morphology', 0.41964285714285715, 7.492661022682715, 1.7732009697610411, 'HP:0001167', 'Abnormal finger morphology'),
(111480, 'HP:0010228', 'Absent epiphyses of the phalanges of the hand', 'XPO:0115789', 'duplicated forelimb digit 5 in regenerating forelimb', 0.44029850746268656, 7.774297771301195, 1.8501382935538648, 'HP:0005918', 'Abnormal finger phalanx morphology'),
(111481, 'HP:0010228', 'Absent epiphyses of the phalanges of the hand', 'XPO:0103282', 'absent forelimb digit 5', 0.421875, 10.497804325958676, 2.1044622115908416, 'UPHENO:0026181', 'absent anatomical entity in the forelimb'),
(111482, 'HP:0010228', 'Absent epiphyses of the phalanges of the hand', 'XPO:0103279', 'absent forelimb digit 2', 0.421875, 10.497804325958676, 2.1044622115908416, 'UPHENO:0026181', 'absent anatomical entity in the forelimb'),
(111483, 'HP:0010228', 'Absent epiphyses of the phalanges of the hand', 'XPO:0102529', 'abnormal forelimb digit 4 morphology', 0.41228070175438597, 7.492661022682715, 1.7575777491876043, 'HP:0001167', 'Abnormal finger morphology'),
(111484, 'HP:0010228', 'Absent epiphyses of the phalanges of the hand', 'XPO:0103634', 'abnormally increased number of forelimb digit', 0.4796747967479675, 7.774297771301195, 1.9310967617670216, 'HP:0005918', 'Abnormal finger phalanx morphology'),
(111485, 'HP:0010228', 'Absent epiphyses of the phalanges of the hand', 'XPO:0103280', 'absent forelimb digit 3', 0.421875, 10.497804325958676, 2.1044622115908416, 'UPHENO:0026181', 'absent anatomical entity in the forelimb'),
(111486, 'HP:0010228', 'Absent epiphyses of the phalanges of the hand', 'XPO:0102598', 'abnormal forelimb digit 3 morphology', 0.41228070175438597, 7.492661022682715, 1.7575777491876043, 'HP:0001167', 'Abnormal finger morphology'),
(111487, 'HP:0010228', 'Absent epiphyses of the phalanges of the hand', 'XPO:0102746', 'abnormal forelimb digit 2 morphology', 0.41228070175438597, 7.492661022682715, 1.7575777491876043, 'HP:0001167', 'Abnormal finger morphology'),
(111488, 'HP:0010228', 'Absent epiphyses of the phalanges of the hand', 'XPO:0103281', 'absent forelimb digit 4', 0.421875, 10.497804325958676, 2.1044622115908416, 'UPHENO:0026181', 'absent anatomical entity in the forelimb'),
(111489, 'HP:0010874', 'Tendon xanthomatosis', 'XPO:0140660', 'abnormally necrotic tendon', 0.45454545454545453, 10.802658907487096, 2.21591956158233, 'UPHENO:0021425', 'abnormal tendon morphology'),
(111490, 'HP:0010874', 'Tendon xanthomatosis', 'XPO:0102615', 'abnormal skin gland morphology', 0.42, 7.420886955069779, 1.7654383368244009, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(111491, 'HP:0010874', 'Tendon xanthomatosis', 'XPO:0102626', 'abnormal granular gland morphology', 0.40384615384615385, 7.420886955069779, 1.7311547172139254, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(111492, 'HP:0010874', 'Tendon xanthomatosis', 'XPO:0128816', 'decreased size of the tendon', 0.43859649122807015, 10.802658907487096, 2.176696646930274, 'UPHENO:0021425', 'abnormal tendon morphology'),
(111493, 'HP:0010874', 'Tendon xanthomatosis', 'XPO:0102806', 'abnormal articular system morphology', 0.43478260869565216, 4.638757693672553, 1.4201588541997616, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(111494, 'HP:0010874', 'Tendon xanthomatosis', 'XPO:0102010', 'abnormal perichondrium morphology', 0.4782608695652174, 6.985637650836012, 1.827828530622157, 'UPHENO:0002712', 'abnormal connective tissue'),
(111495, 'HP:0010874', 'Tendon xanthomatosis', 'XPO:0102097', 'abnormal skeletal system morphology', 0.4444444444444444, 4.638757693672553, 1.4358516936218344, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(111496, 'HP:0010874', 'Tendon xanthomatosis', 'XPO:0102272', 'abnormal notochordal sheath morphology', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(111497, 'HP:0010874', 'Tendon xanthomatosis', 'XPO:0107372', 'abnormal flexural organ morphology', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(111498, 'HP:0010874', 'Tendon xanthomatosis', 'XPO:0140123', 'abnormally necrotic perichondrial cell', 0.4074074074074074, 6.985637650836012, 1.6870093433098323, 'UPHENO:0002712', 'abnormal connective tissue'),
(111499, 'HP:0010874', 'Tendon xanthomatosis', 'XPO:0102980', 'abnormal perichordal tissue morphology', 0.4489795918367347, 6.985637650836012, 1.7709908924643512, 'UPHENO:0002712', 'abnormal connective tissue'),
(111500, 'HP:0010874', 'Tendon xanthomatosis', 'XPO:0102727', 'abnormal skin seromucous gland morphology', 0.40384615384615385, 7.420886955069779, 1.7311547172139254, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(111501, 'HP:0010874', 'Tendon xanthomatosis', 'XPO:0102009', 'abnormal connective tissue morphology', 0.4090909090909091, 6.985637650836012, 1.6904913064432443, 'UPHENO:0002712', 'abnormal connective tissue'),
(111502, 'HP:0010874', 'Tendon xanthomatosis', 'XPO:0102542', 'abnormal vacuolated notochordal tissue morphology', 0.4489795918367347, 6.985637650836012, 1.7709908924643512, 'UPHENO:0002712', 'abnormal connective tissue'),
(111503, 'HP:0010874', 'Tendon xanthomatosis', 'XPO:0141723', 'abnormal posterior notochord morphology', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(111504, 'HP:0010874', 'Tendon xanthomatosis', 'XPO:0102567', 'abnormal skeleton morphology', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(111505, 'HP:0010874', 'Tendon xanthomatosis', 'XPO:0102217', 'abnormal elastica externa morphology', 0.4444444444444444, 4.638757693672553, 1.4358516936218344, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(111506, 'HP:0010874', 'Tendon xanthomatosis', 'XPO:0102561', 'abnormal dermis morphology', 0.4117647058823529, 7.420886955069779, 1.7480444314835069, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(111507, 'HP:0010874', 'Tendon xanthomatosis', 'XPO:0128132', 'decreased size of the perichondrium', 0.4074074074074074, 6.985637650836012, 1.6870093433098323, 'UPHENO:0002712', 'abnormal connective tissue'),
(111508, 'HP:0010874', 'Tendon xanthomatosis', 'XPO:0140722', 'abnormally necrotic intersomitic tendon', 0.4098360655737705, 10.802658907487096, 2.104119584144389, 'UPHENO:0021425', 'abnormal tendon morphology'),
(111509, 'HP:0010874', 'Tendon xanthomatosis', 'XPO:0101860', 'abnormal skeletal subdivision morphology', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(111510, 'HP:0010874', 'Tendon xanthomatosis', 'XPO:0102139', 'abnormal skin morphology', 0.42, 7.420886955069779, 1.7654383368244009, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(111511, 'HP:0010874', 'Tendon xanthomatosis', 'XPO:0140043', 'abnormally necrotic perichondrium', 0.4230769230769231, 6.985637650836012, 1.719145742235371, 'UPHENO:0002712', 'abnormal connective tissue'),
(111512, 'HP:0010874', 'Tendon xanthomatosis', 'XPO:0141719', 'abnormal anterior notochord morphology', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(111513, 'HP:0010874', 'Tendon xanthomatosis', 'XPO:0102514', 'abnormal perichondrial cell morphology', 0.44, 6.985637650836012, 1.753191537273622, 'UPHENO:0002712', 'abnormal connective tissue'),
(111514, 'HP:0010874', 'Tendon xanthomatosis', 'XPO:0129612', 'increased size of the perichondrium', 0.4074074074074074, 6.985637650836012, 1.6870093433098323, 'UPHENO:0002712', 'abnormal connective tissue'),
(111515, 'HP:0010874', 'Tendon xanthomatosis', 'XPO:0130294', 'increased size of the tendon', 0.43859649122807015, 10.802658907487096, 2.176696646930274, 'UPHENO:0021425', 'abnormal tendon morphology'),
(111516, 'HP:0010874', 'Tendon xanthomatosis', 'XPO:0102728', 'abnormal tendon morphology', 0.5208333333333334, 10.802658907487096, 2.3720001786782245, 'UPHENO:0021425', 'abnormal tendon morphology'),
(111517, 'HP:0010874', 'Tendon xanthomatosis', 'XPO:0102054', 'abnormal notochord morphology', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(111518, 'HP:0010874', 'Tendon xanthomatosis', 'XPO:0103234', 'abnormal intersomitic tendon morphology', 0.4716981132075472, 10.802658907487096, 2.257342203629385, 'UPHENO:0021425', 'abnormal tendon morphology'),
(111519, 'HP:0100343', 'Tibial deviation of the 3rd toe', 'XPO:0103778', 'decreased size of the hindlimb digit in the regenerating hindlimb', 0.42, 7.639349617137506, 1.791236120448042, 'HP:0001780', 'Abnormal toe morphology'),
(111520, 'HP:0100343', 'Tibial deviation of the 3rd toe', 'XPO:0128497', 'decreased size of the digit-joint region', 0.4533333333333333, 6.466375519622663, 1.7121400552804105, 'UPHENO:0086700', 'abnormal digit morphology'),
(111521, 'HP:0100343', 'Tibial deviation of the 3rd toe', 'XPO:0129977', 'increased size of the digit-joint region', 0.4533333333333333, 6.466375519622663, 1.7121400552804105, 'UPHENO:0086700', 'abnormal digit morphology'),
(111522, 'HP:0100343', 'Tibial deviation of the 3rd toe', 'XPO:0101248', 'abnormal digit-joint region', 0.42424242424242425, 6.393467666143939, 1.6469305455909364, 'UPHENO:0002905', 'abnormal digit'),
(111523, 'HP:0100343', 'Tibial deviation of the 3rd toe', 'XPO:0102051', 'abnormal hindlimb digit 2 morphology', 0.49411764705882355, 7.639349617137506, 1.9428683583505366, 'HP:0001780', 'Abnormal toe morphology'),
(111524, 'HP:0100343', 'Tibial deviation of the 3rd toe', 'XPO:0100178', 'abnormal digit', 0.4444444444444444, 6.393467666143939, 1.6856871551248356, 'HP:0011297', 'Abnormal digit morphology'),
(111525, 'HP:0100343', 'Tibial deviation of the 3rd toe', 'XPO:0133379', 'fused hindlimb digits part of regenerating hindlimb', 0.42424242424242425, 7.639349617137506, 1.800260037108487, 'HP:0001780', 'Abnormal toe morphology'),
(111526, 'HP:0100343', 'Tibial deviation of the 3rd toe', 'XPO:0102457', 'abnormal claw of hindlimb digit 2 morphology', 0.4117647058823529, 7.639349617137506, 1.773588043552699, 'HP:0001780', 'Abnormal toe morphology'),
(111527, 'HP:0100343', 'Tibial deviation of the 3rd toe', 'XPO:0139924', 'abnormally necrotic hindlimb digit 1', 0.44680851063829785, 7.639349617137506, 1.8475189916962858, 'UPHENO:0088132', 'abnormal pedal digit morphology'),
(111528, 'HP:0100343', 'Tibial deviation of the 3rd toe', 'XPO:0102566', 'abnormal claw primordium morphology', 0.5121951219512195, 7.639349617137506, 1.9780893834146491, 'UPHENO:0088132', 'abnormal pedal digit morphology'),
(111529, 'HP:0100343', 'Tibial deviation of the 3rd toe', 'XPO:0129321', 'decreased size of the hindlimb digit 4', 0.4375, 7.639349617137506, 1.8281727099750884, 'HP:0001780', 'Abnormal toe morphology'),
(111530, 'HP:0100343', 'Tibial deviation of the 3rd toe', 'XPO:0102880', 'abnormal digit-joint region morphology', 0.4927536231884058, 6.466375519622663, 1.7850294020522122, 'UPHENO:0086700', 'abnormal digit morphology'),
(111531, 'HP:0100343', 'Tibial deviation of the 3rd toe', 'XPO:0103460', 'bifurcated hindlimb digit 1', 0.4158415841584158, 7.639349617137506, 1.7823465562932612, 'HP:0001780', 'Abnormal toe morphology'),
(111532, 'HP:0100343', 'Tibial deviation of the 3rd toe', 'XPO:0128670', 'decreased size of the claw primordium', 0.47191011235955055, 7.639349617137506, 1.8987064902657413, 'UPHENO:0088132', 'abnormal pedal digit morphology'),
(111533, 'HP:0100343', 'Tibial deviation of the 3rd toe', 'XPO:0102797', 'abnormal claw of hindlimb digit 3 morphology', 0.4117647058823529, 7.639349617137506, 1.773588043552699, 'HP:0001780', 'Abnormal toe morphology'),
(111534, 'HP:0100343', 'Tibial deviation of the 3rd toe', 'XPO:0102180', 'abnormal hindlimb digit 3 morphology', 0.49411764705882355, 7.639349617137506, 1.9428683583505366, 'HP:0001780', 'Abnormal toe morphology'),
(111535, 'HP:0100343', 'Tibial deviation of the 3rd toe', 'XPO:0103462', 'bifurcated hindlimb digit 3', 0.4158415841584158, 7.639349617137506, 1.7823465562932612, 'UPHENO:0088132', 'abnormal pedal digit morphology'),
(111536, 'HP:0100343', 'Tibial deviation of the 3rd toe', 'XPO:0140474', 'abnormally necrotic hindlimb digit 2', 0.44680851063829785, 7.639349617137506, 1.8475189916962858, 'HP:0001780', 'Abnormal toe morphology'),
(111537, 'HP:0100343', 'Tibial deviation of the 3rd toe', 'XPO:0141568', 'abnormal digit-joint region morphology in the regenerating forelimb', 0.4533333333333333, 6.466375519622663, 1.7121400552804105, 'UPHENO:0086700', 'abnormal digit morphology'),
(111538, 'HP:0100343', 'Tibial deviation of the 3rd toe', 'XPO:0139979', 'abnormally necrotic claw primordium', 0.4827586206896552, 7.639349617137506, 1.920406697586568, 'UPHENO:0088132', 'abnormal pedal digit morphology'),
(111539, 'HP:0100343', 'Tibial deviation of the 3rd toe', 'XPO:0140680', 'abnormally necrotic hindlimb digit 3', 0.44680851063829785, 7.639349617137506, 1.8475189916962858, 'UPHENO:0088132', 'abnormal pedal digit morphology'),
(111540, 'HP:0100343', 'Tibial deviation of the 3rd toe', 'XPO:0103627', 'abnormally increased number of hindlimb digit', 0.40425531914893614, 7.639349617137506, 1.7573410931194393, 'HP:0001780', 'Abnormal toe morphology'),
(111541, 'HP:0100343', 'Tibial deviation of the 3rd toe', 'XPO:0130797', 'increased size of the hindlimb digit 4', 0.4375, 7.639349617137506, 1.8281727099750884, 'UPHENO:0088132', 'abnormal pedal digit morphology'),
(111542, 'HP:0100343', 'Tibial deviation of the 3rd toe', 'XPO:0101869', 'abnormal claw morphology', 0.42424242424242425, 7.639349617137506, 1.800260037108487, 'UPHENO:0088132', 'abnormal pedal digit morphology'),
(111543, 'HP:0100343', 'Tibial deviation of the 3rd toe', 'XPO:0103044', 'abnormal claw of hindlimb digit 4 morphology', 0.4117647058823529, 7.639349617137506, 1.773588043552699, 'HP:0001780', 'Abnormal toe morphology'),
