(32240, 'HP:0030243', 'Hepatic vein thrombosis', 'XPO:0101326', 'abnormal cementoblast', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(32241, 'HP:0030243', 'Hepatic vein thrombosis', 'XPO:0100104', 'abnormal embryonic structure', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(32242, 'HP:0030243', 'Hepatic vein thrombosis', 'XPO:0107278', 'abnormal medial region', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(32243, 'HP:0030243', 'Hepatic vein thrombosis', 'XPO:0101575', 'abnormal vitelline membrane', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(32244, 'HP:0030243', 'Hepatic vein thrombosis', 'XPO:0100081', 'abnormal anatomical entity in vitro', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(32245, 'HP:0030243', 'Hepatic vein thrombosis', 'XPO:0100308', 'abnormal early embryonic cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(32246, 'HP:0030243', 'Hepatic vein thrombosis', 'XPO:0100802', 'abnormal exocrine cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(32247, 'HP:0030243', 'Hepatic vein thrombosis', 'XPO:0100976', 'abnormal multiciliated cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(32248, 'HP:0030243', 'Hepatic vein thrombosis', 'XPO:0100549', 'abnormal mitotic cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(32249, 'HP:0030243', 'Hepatic vein thrombosis', 'XPO:0101535', 'abnormal absorptive cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(32250, 'HP:0030243', 'Hepatic vein thrombosis', 'XPO:0100862', 'abnormal blastomere V1', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(32251, 'HP:0030243', 'Hepatic vein thrombosis', 'XPO:0100025', 'abnormal oocyte', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(32252, 'HP:0030243', 'Hepatic vein thrombosis', 'XPO:0101587', 'abnormal hemangioblast', 0.48148148148148145, 5.574066539846944, 1.6382337487311942, 'UPHENO:0004459', 'abnormal hematopoietic system'),
(32253, 'HP:0030243', 'Hepatic vein thrombosis', 'XPO:0141771', 'abnormal urea homeostasis', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(32254, 'HP:0030243', 'Hepatic vein thrombosis', 'XPO:0100274', 'abnormal sensory system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(32255, 'HP:0030243', 'Hepatic vein thrombosis', 'XPO:0100239', 'abnormal acellular anatomical structure', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(32256, 'HP:0030243', 'Hepatic vein thrombosis', 'XPO:0100688', 'abnormal adipose tissue', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(32257, 'HP:0030243', 'Hepatic vein thrombosis', 'XPO:0107253', 'abnormal enteric nervous system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(32258, 'HP:0030243', 'Hepatic vein thrombosis', 'XPO:0100176', 'abnormal stage VI oocyte', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(32259, 'HP:0030243', 'Hepatic vein thrombosis', 'XPO:0100084', 'abnormal anatomical group', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(32260, 'HP:0030243', 'Hepatic vein thrombosis', 'XPO:0101056', 'abnormal anterior ventral blood island', 0.4482758620689655, 5.574066539846944, 1.5807338433081215, 'UPHENO:0004459', 'abnormal hematopoietic system'),
(32261, 'HP:0030243', 'Hepatic vein thrombosis', 'XPO:0101451', 'abnormal dorsal lymph space', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(32262, 'HP:0030243', 'Hepatic vein thrombosis', 'XPO:0102004', 'abnormal hematological system morphology', 0.40625, 5.574066539846944, 1.5048137864243607, 'HP:0001871', 'Abnormality of blood and blood-forming tissues'),
(32263, 'HP:0030243', 'Hepatic vein thrombosis', 'XPO:0100465', 'abnormal skeletal system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(32264, 'HP:0030243', 'Hepatic vein thrombosis', 'XPO:0101347', 'abnormal hindlimb region', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(32265, 'HP:0030243', 'Hepatic vein thrombosis', 'XPO:0100437', 'abnormal proepicardium', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(32266, 'HP:0030243', 'Hepatic vein thrombosis', 'XPO:0100344', 'abnormal portion of organism substance', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(32267, 'HP:0030243', 'Hepatic vein thrombosis', 'XPO:0131667', 'abnormal actin cytoskeleton', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(32268, 'HP:0030243', 'Hepatic vein thrombosis', 'XPO:0101132', 'abnormal apoptotic cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(32269, 'HP:0030243', 'Hepatic vein thrombosis', 'XPO:0101220', 'abnormal centriole', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(32270, 'HP:0030243', 'Hepatic vein thrombosis', 'XPO:0101136', 'abnormal ooplasm', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(32271, 'HP:0030243', 'Hepatic vein thrombosis', 'XPO:0100585', 'abnormal elastica externa', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(32272, 'HP:0030243', 'Hepatic vein thrombosis', 'XPO:0100917', 'abnormal stage III oocyte', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(32273, 'HP:0030243', 'Hepatic vein thrombosis', 'XPO:0100258', 'abnormal organ part', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(32274, 'HP:0030243', 'Hepatic vein thrombosis', 'XPO:0100852', 'abnormal interdigital region', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(32275, 'HP:0030243', 'Hepatic vein thrombosis', 'XPO:0101468', 'abnormal stage I oocyte', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(32276, 'HP:0030243', 'Hepatic vein thrombosis', 'XPO:0107339', 'abnormal yolk platelet', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(32277, 'HP:0030243', 'Hepatic vein thrombosis', 'XPO:0131675', 'abnormal spindle microtubule', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(32278, 'HP:0030243', 'Hepatic vein thrombosis', 'XPO:0101311', 'abnormal bottle cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(32279, 'HP:0030243', 'Hepatic vein thrombosis', 'XPO:0100503', 'abnormal blastomere D2', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(32280, 'HP:0030243', 'Hepatic vein thrombosis', 'XPO:0100547', 'abnormal blastomere V2', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(32281, 'HP:0030243', 'Hepatic vein thrombosis', 'XPO:0101061', 'abnormal plasma membrane', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(32282, 'HP:0030243', 'Hepatic vein thrombosis', 'XPO:0141315', 'abnormal anatomical region', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(32283, 'HP:0030243', 'Hepatic vein thrombosis', 'XPO:0100673', 'abnormal anterior dorsal lateral plate region', 0.40625, 5.574066539846944, 1.5048137864243607, 'UPHENO:0004459', 'abnormal hematopoietic system'),
(32284, 'HP:0030243', 'Hepatic vein thrombosis', 'XPO:0101240', 'abnormal ciliated non-epidermal cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(32285, 'HP:0030243', 'Hepatic vein thrombosis', 'XPO:0101480', 'abnormal stage V oocyte', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(32286, 'HP:0030243', 'Hepatic vein thrombosis', 'XPO:0100218', 'abnormal epithelial cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(32287, 'HP:0030243', 'Hepatic vein thrombosis', 'XPO:0100581', 'abnormal immune system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(32288, 'HP:0030243', 'Hepatic vein thrombosis', 'XPO:0131687', 'abnormal astral microtubule', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(32289, 'HP:0030243', 'Hepatic vein thrombosis', 'XPO:0100205', 'abnormal limb segment', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(32290, 'HP:0030243', 'Hepatic vein thrombosis', 'XPO:0100372', 'abnormal hematological system', 0.5652173913043478, 5.574066539846944, 1.7749815065541226, 'UPHENO:0004459', 'abnormal hematopoietic system'),
(32291, 'HP:0030243', 'Hepatic vein thrombosis', 'XPO:0100337', 'abnormal zygote', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(32292, 'HP:0030243', 'Hepatic vein thrombosis', 'XPO:0100599', 'abnormal adult immune system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(32293, 'HP:0030243', 'Hepatic vein thrombosis', 'XPO:0100665', 'abnormal egg jelly', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(32294, 'HP:0030243', 'Hepatic vein thrombosis', 'XPO:0101297', 'abnormal barrier cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(32295, 'HP:0030243', 'Hepatic vein thrombosis', 'XPO:0100762', 'abnormal intersomitic region', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(32296, 'HP:0030243', 'Hepatic vein thrombosis', 'XPO:0141748', 'abnormal gas homeostasis', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(32297, 'HP:0030243', 'Hepatic vein thrombosis', 'XPO:0101497', 'abnormal ciliary axoneme', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(32298, 'HP:0030243', 'Hepatic vein thrombosis', 'XPO:0101461', 'abnormal sperm entry point', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(32299, 'HP:0030243', 'Hepatic vein thrombosis', 'XPO:0100307', 'abnormal blastomere', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(32300, 'HP:0030243', 'Hepatic vein thrombosis', 'XPO:0100026', 'abnormal germ cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(32301, 'HP:0030243', 'Hepatic vein thrombosis', 'XPO:0100423', 'abnormal process', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(32302, 'HP:0030243', 'Hepatic vein thrombosis', 'XPO:0141266', 'abnormal surface breathing', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(32303, 'HP:0030243', 'Hepatic vein thrombosis', 'XPO:0101072', 'abnormal mitochondrial cloud', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(32304, 'HP:0030243', 'Hepatic vein thrombosis', 'XPO:0100392', 'abnormal cilium', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(32305, 'HP:0030243', 'Hepatic vein thrombosis', 'XPO:0100653', 'abnormal myoblast', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(32306, 'HP:0030243', 'Hepatic vein thrombosis', 'XPO:0101113', 'abnormal stage IV oocyte', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(32307, 'HP:0030243', 'Hepatic vein thrombosis', 'XPO:0141776', 'abnormal metabolic process', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(32308, 'HP:0030243', 'Hepatic vein thrombosis', 'XPO:0131725', 'abnormal phosphorylation of RNA polymerase II C-terminal domain', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(32309, 'HP:0030243', 'Hepatic vein thrombosis', 'XPO:0100070', 'abnormal anatomical system', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(32310, 'HP:0030243', 'Hepatic vein thrombosis', 'XPO:0131723', 'abnormal pathway-restricted SMAD protein phosphorylation', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(32311, 'HP:0030243', 'Hepatic vein thrombosis', 'XPO:0101569', 'abnormal activin-induced ectoderm', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(32312, 'HP:0030243', 'Hepatic vein thrombosis', 'XPO:0101547', 'abnormal lampbrush chromosome', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(32313, 'HP:0030243', 'Hepatic vein thrombosis', 'XPO:0100704', 'abnormal Merkel cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(32314, 'HP:0030243', 'Hepatic vein thrombosis', 'XPO:0101448', 'abnormal myelin accumulating cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(32315, 'HP:0030243', 'Hepatic vein thrombosis', 'XPO:0101389', 'abnormal wedge region', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(32316, 'HP:0030243', 'Hepatic vein thrombosis', 'XPO:0101004', 'abnormal acid secreting cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(32317, 'HP:0030243', 'Hepatic vein thrombosis', 'XPO:0101200', 'abnormal joint region', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(32318, 'HP:0030243', 'Hepatic vein thrombosis', 'XPO:0107261', 'abnormal dorsal-ventral axis', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(32319, 'HP:0030243', 'Hepatic vein thrombosis', 'XPO:0141272', 'absent surface breathing', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(32320, 'HP:0030243', 'Hepatic vein thrombosis', 'XPO:0100887', 'abnormal right-dorsal blastomere', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(32321, 'HP:0030243', 'Hepatic vein thrombosis', 'XPO:0107284', 'abnormal migrating myoblast', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(32322, 'HP:0030243', 'Hepatic vein thrombosis', 'XPO:0131685', 'abnormal cortical actin cytoskeleton', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(32323, 'HP:0030243', 'Hepatic vein thrombosis', 'XPO:0100003', 'abnormal organism subdivision', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(32324, 'HP:0030243', 'Hepatic vein thrombosis', 'XPO:0101228', 'abnormal mesenchymal stem cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(32325, 'HP:0030243', 'Hepatic vein thrombosis', 'XPO:0101107', 'abnormal erythroid cell', 0.48148148148148145, 5.574066539846944, 1.6382337487311942, 'HP:0001871', 'Abnormality of blood and blood-forming tissues'),
(32326, 'HP:0030243', 'Hepatic vein thrombosis', 'XPO:0100481', 'abnormal anatomical line', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(32327, 'HP:0030243', 'Hepatic vein thrombosis', 'XPO:0101366', 'abnormal morula cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(32328, 'HP:0030243', 'Hepatic vein thrombosis', 'XPO:0100386', 'abnormal limb', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(32329, 'HP:0030243', 'Hepatic vein thrombosis', 'XPO:0115512', 'abnormally semi-erect whole organism', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(32330, 'HP:0030243', 'Hepatic vein thrombosis', 'XPO:0142057', 'abnormal desmosome', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(32331, 'HP:0030243', 'Hepatic vein thrombosis', 'XPO:0107259', 'abnormal animal-vegetal axis', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(32332, 'HP:0030243', 'Hepatic vein thrombosis', 'XPO:0100108', 'abnormal cell part', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(32333, 'HP:0030243', 'Hepatic vein thrombosis', 'XPO:0100902', 'abnormal spermatocyte', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(32334, 'HP:0030243', 'Hepatic vein thrombosis', 'XPO:0100638', 'abnormal polar body', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(32335, 'HP:0030243', 'Hepatic vein thrombosis', 'XPO:0100989', 'abnormal right blastomere', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(32336, 'HP:0030243', 'Hepatic vein thrombosis', 'XPO:0107270', 'abnormal proximal-distal axis', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(32337, 'HP:0030243', 'Hepatic vein thrombosis', 'XPO:0100295', 'abnormal extracellular matrix', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(32338, 'HP:0030243', 'Hepatic vein thrombosis', 'XPO:0141738', 'abnormal carbon dioxide homeostasis', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(32339, 'HP:0030243', 'Hepatic vein thrombosis', 'XPO:0101221', 'abnormal larval immune system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(32340, 'HP:0030243', 'Hepatic vein thrombosis', 'XPO:0131666', 'abnormal adherens junction', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(32341, 'HP:0030243', 'Hepatic vein thrombosis', 'XPO:0101513', 'abnormal basal body', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(32342, 'HP:0030243', 'Hepatic vein thrombosis', 'XPO:0100551', 'abnormal oocyte cortex', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(32343, 'HP:0030243', 'Hepatic vein thrombosis', 'XPO:0100533', 'abnormal melanoblast', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(32344, 'HP:0030243', 'Hepatic vein thrombosis', 'XPO:0100317', 'abnormal respiratory system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(32345, 'HP:0030243', 'Hepatic vein thrombosis', 'XPO:0100587', 'abnormal vestibuloauditory system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(32346, 'HP:0030243', 'Hepatic vein thrombosis', 'XPO:0100006', 'abnormal anatomical structure', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(32347, 'HP:0030243', 'Hepatic vein thrombosis', 'XPO:0102455', 'abnormal blood morphology', 0.40625, 5.574066539846944, 1.5048137864243607, 'UPHENO:0004459', 'abnormal hematopoietic system'),
(32348, 'HP:0030243', 'Hepatic vein thrombosis', 'XPO:0100728', 'abnormal cell condensation', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(32349, 'HP:0030243', 'Hepatic vein thrombosis', 'XPO:0107323', 'abnormal thrombocyte', 0.41935483870967744, 5.574066539846944, 1.5288923359002506, 'HP:0001871', 'Abnormality of blood and blood-forming tissues'),
(32350, 'HP:0025619', 'Elevated plasma cell count', 'XPO:0103067', 'abnormal paracrine cell morphology', 0.41304347826086957, 5.43643956286526, 1.4984945466703803, 'HP:0025461', 'Abnormal cell morphology'),
(32351, 'HP:0025619', 'Elevated plasma cell count', 'XPO:0103219', 'abnormal hemangioblast morphology', 0.42, 5.574066539846944, 1.5300679549404714, 'UPHENO:0004459', 'abnormal hematopoietic system'),
(32352, 'HP:0025619', 'Elevated plasma cell count', 'XPO:0103005', 'abnormal oxygen accumulating cell morphology', 0.41304347826086957, 5.43643956286526, 1.4984945466703803, 'HP:0025461', 'Abnormal cell morphology'),
(32353, 'HP:0025619', 'Elevated plasma cell count', 'XPO:0103150', 'abnormal B cell morphology', 0.43137254901960786, 6.786309419308587, 1.7109727036522004, 'UPHENO:0087123', 'abnormal immune system morphology'),
(32354, 'HP:0025619', 'Elevated plasma cell count', 'XPO:0102386', 'abnormal electrically active cell morphology', 0.41304347826086957, 5.43643956286526, 1.4984945466703803, 'HP:0025461', 'Abnormal cell morphology'),
(32355, 'HP:0025619', 'Elevated plasma cell count', 'XPO:0102423', 'abnormal multiciliated cell precursor morphology', 0.41304347826086957, 5.43643956286526, 1.4984945466703803, 'HP:0025461', 'Abnormal cell morphology'),
(32356, 'HP:0025619', 'Elevated plasma cell count', 'XPO:0102636', 'abnormal acid secreting cell morphology', 0.41304347826086957, 5.43643956286526, 1.4984945466703803, 'HP:0025461', 'Abnormal cell morphology'),
(32357, 'HP:0025619', 'Elevated plasma cell count', 'XPO:0103099', 'abnormal alkali secreting cell morphology', 0.41304347826086957, 5.43643956286526, 1.4984945466703803, 'HP:0025461', 'Abnormal cell morphology'),
(32358, 'HP:0025619', 'Elevated plasma cell count', 'XPO:0139717', 'abnormally necrotic cell', 0.40425531914893614, 5.43643956286526, 1.4824674062251753, 'HP:0025461', 'Abnormal cell morphology'),
(32359, 'HP:0025619', 'Elevated plasma cell count', 'XPO:0101917', 'abnormal progenitor cell morphology', 0.41304347826086957, 5.43643956286526, 1.4984945466703803, 'HP:0025461', 'Abnormal cell morphology'),
(32360, 'HP:0025619', 'Elevated plasma cell count', 'XPO:0125284', 'absent thymocyte', 0.4358974358974359, 8.504690711543915, 1.9254020032872958, 'UPHENO:0084888', 'abnormal lymphocyte morphology'),
(32361, 'HP:0025619', 'Elevated plasma cell count', 'XPO:0103167', 'abnormal absorptive cell morphology', 0.41304347826086957, 5.43643956286526, 1.4984945466703803, 'HP:0025461', 'Abnormal cell morphology'),
(32362, 'HP:0025619', 'Elevated plasma cell count', 'XPO:0102109', 'abnormal pericyte morphology', 0.41304347826086957, 5.43643956286526, 1.4984945466703803, 'HP:0025461', 'Abnormal cell morphology'),
(32363, 'HP:0025619', 'Elevated plasma cell count', 'XPO:0102165', 'abnormal melanoblast morphology', 0.41304347826086957, 5.43643956286526, 1.4984945466703803, 'HP:0025461', 'Abnormal cell morphology'),
(32364, 'HP:0025619', 'Elevated plasma cell count', 'XPO:0101636', 'abnormal cell morphology', 0.4318181818181818, 5.43643956286526, 1.532172786470543, 'HP:0025461', 'Abnormal cell morphology'),
(32365, 'HP:0025619', 'Elevated plasma cell count', 'XPO:0140117', 'abnormally necrotic thymocyte', 0.43037974683544306, 8.504690711543915, 1.9131771050658155, 'UPHENO:0084888', 'abnormal lymphocyte morphology'),
(32366, 'HP:0025619', 'Elevated plasma cell count', 'XPO:0102873', 'abnormal nucleate erythrocyte morphology', 0.41304347826086957, 5.43643956286526, 1.4984945466703803, 'HP:0025461', 'Abnormal cell morphology'),
(32367, 'HP:0025619', 'Elevated plasma cell count', 'XPO:0102285', 'abnormal myoblast morphology', 0.41304347826086957, 5.43643956286526, 1.4984945466703803, 'HP:0025461', 'Abnormal cell morphology'),
(32368, 'HP:0025619', 'Elevated plasma cell count', 'XPO:0103082', 'abnormal myeloid cell morphology', 0.42, 5.574066539846944, 1.5300679549404714, 'HP:0001871', 'Abnormality of blood and blood-forming tissues'),
(32369, 'HP:0025619', 'Elevated plasma cell count', 'XPO:0103080', 'abnormal myelin accumulating cell morphology', 0.41304347826086957, 5.43643956286526, 1.4984945466703803, 'HP:0025461', 'Abnormal cell morphology'),
(32370, 'HP:0025619', 'Elevated plasma cell count', 'XPO:0102081', 'abnormal lymphocyte morphology', 0.4489795918367347, 6.786309419308587, 1.7455413009032348, 'UPHENO:0087123', 'abnormal immune system morphology'),
(32371, 'HP:0025619', 'Elevated plasma cell count', 'XPO:0102869', 'abnormal mucus secreting cell morphology', 0.41304347826086957, 5.43643956286526, 1.4984945466703803, 'HP:0025461', 'Abnormal cell morphology'),
(32372, 'HP:0025619', 'Elevated plasma cell count', 'XPO:0101658', 'abnormal germ cell morphology', 0.41304347826086957, 5.43643956286526, 1.4984945466703803, 'HP:0025461', 'Abnormal cell morphology'),
(32373, 'HP:0025619', 'Elevated plasma cell count', 'XPO:0101804', 'abnormal stem cell morphology', 0.41304347826086957, 5.43643956286526, 1.4984945466703803, 'HP:0025461', 'Abnormal cell morphology'),
(32374, 'HP:0025619', 'Elevated plasma cell count', 'XPO:0102080', 'abnormal thymocyte morphology', 0.4594594594594595, 8.504690711543915, 1.9767550675781391, 'UPHENO:0084888', 'abnormal lymphocyte morphology'),
(32375, 'HP:0025619', 'Elevated plasma cell count', 'XPO:0102715', 'abnormal T cell morphology', 0.43137254901960786, 6.786309419308587, 1.7109727036522004, 'UPHENO:0087123', 'abnormal immune system morphology'),
(32376, 'HP:0025619', 'Elevated plasma cell count', 'XPO:0102739', 'abnormal erythroid cell morphology', 0.42, 5.574066539846944, 1.5300679549404714, 'HP:0001871', 'Abnormality of blood and blood-forming tissues'),
(32377, 'HP:0025619', 'Elevated plasma cell count', 'XPO:0101921', 'abnormal chondroblast morphology', 0.41304347826086957, 5.43643956286526, 1.4984945466703803, 'HP:0025461', 'Abnormal cell morphology'),
(32378, 'HP:0025619', 'Elevated plasma cell count', 'XPO:0101969', 'abnormal zygote morphology', 0.41304347826086957, 5.43643956286526, 1.4984945466703803, 'HP:0025461', 'Abnormal cell morphology'),
(32379, 'HP:0025619', 'Elevated plasma cell count', 'XPO:0141478', 'abnormally necrotic lymphoblast', 0.41509433962264153, 6.786309419308587, 1.6783797624145764, 'UPHENO:0087123', 'abnormal immune system morphology'),
(32380, 'HP:0025619', 'Elevated plasma cell count', 'XPO:0141503', 'abnormal lymphoblast morphology', 0.4489795918367347, 6.786309419308587, 1.7455413009032348, 'UPHENO:0087123', 'abnormal immune system morphology'),
(32381, 'HP:0025619', 'Elevated plasma cell count', 'XPO:0102434', 'abnormal exocrine cell morphology', 0.41304347826086957, 5.43643956286526, 1.4984945466703803, 'HP:0025461', 'Abnormal cell morphology'),
(32382, 'HP:0025619', 'Elevated plasma cell count', 'XPO:0102929', 'abnormal barrier cell morphology', 0.41304347826086957, 5.43643956286526, 1.4984945466703803, 'HP:0025461', 'Abnormal cell morphology'),
(32383, 'HP:0025619', 'Elevated plasma cell count', 'XPO:0102958', 'abnormal cementoblast morphology', 0.41304347826086957, 5.43643956286526, 1.4984945466703803, 'HP:0025461', 'Abnormal cell morphology'),
(32384, 'HP:0025619', 'Elevated plasma cell count', 'XPO:0102323', 'abnormal keratin accumulating cell morphology', 0.41304347826086957, 5.43643956286526, 1.4984945466703803, 'HP:0025461', 'Abnormal cell morphology'),
(32385, 'HP:0025619', 'Elevated plasma cell count', 'XPO:0102181', 'abnormal mitotic cell morphology', 0.41304347826086957, 5.43643956286526, 1.4984945466703803, 'HP:0025461', 'Abnormal cell morphology'),
(32386, 'HP:0025619', 'Elevated plasma cell count', 'XPO:0102965', 'abnormal barrier epithelial cell morphology', 0.41304347826086957, 5.43643956286526, 1.4984945466703803, 'HP:0025461', 'Abnormal cell morphology'),
(32387, 'HP:0025619', 'Elevated plasma cell count', 'XPO:0102764', 'abnormal apoptotic cell morphology', 0.41304347826086957, 5.43643956286526, 1.4984945466703803, 'HP:0025461', 'Abnormal cell morphology'),
(32388, 'HP:0025619', 'Elevated plasma cell count', 'XPO:0102347', 'abnormal ciliated cell morphology', 0.41304347826086957, 5.43643956286526, 1.4984945466703803, 'HP:0025461', 'Abnormal cell morphology'),
(32389, 'HP:0025619', 'Elevated plasma cell count', 'XPO:0102446', 'abnormal natural killer cell morphology', 0.41509433962264153, 6.786309419308587, 1.6783797624145764, 'UPHENO:0087123', 'abnormal immune system morphology'),
(32390, 'HP:0025619', 'Elevated plasma cell count', 'XPO:0102336', 'abnormal Merkel cell morphology', 0.41304347826086957, 5.43643956286526, 1.4984945466703803, 'HP:0025461', 'Abnormal cell morphology'),
(32391, 'HP:0025619', 'Elevated plasma cell count', 'XPO:0139951', 'abnormally necrotic lymphocyte', 0.41509433962264153, 6.786309419308587, 1.6783797624145764, 'UPHENO:0087123', 'abnormal immune system morphology'),
(32392, 'HP:0010338', 'Deviation of the 4th toe', 'XPO:0103627', 'abnormally increased number of hindlimb digit', 0.41304347826086957, 7.639349617137506, 1.776339927354367, 'HP:0001780', 'Abnormal toe morphology'),
(32393, 'HP:0010338', 'Deviation of the 4th toe', 'XPO:0103778', 'decreased size of the hindlimb digit in the regenerating hindlimb', 0.42857142857142855, 7.639349617137506, 1.8094217249644198, 'HP:0001780', 'Abnormal toe morphology'),
(32394, 'HP:0010338', 'Deviation of the 4th toe', 'XPO:0103461', 'bifurcated hindlimb digit 2', 0.42424242424242425, 7.639349617137506, 1.800260037108487, 'UPHENO:0088132', 'abnormal pedal digit morphology'),
(32395, 'HP:0010338', 'Deviation of the 4th toe', 'XPO:0102948', 'abnormal hindlimb digit 5 morphology', 0.5060240963855421, 7.639349617137506, 1.9661370722778317, 'UPHENO:0088132', 'abnormal pedal digit morphology'),
(32396, 'HP:0010338', 'Deviation of the 4th toe', 'XPO:0139962', 'abnormally necrotic digit', 0.4594594594594595, 6.466375519622663, 1.723669748213883, 'UPHENO:0086700', 'abnormal digit morphology'),
(32397, 'HP:0010338', 'Deviation of the 4th toe', 'XPO:0141208', 'abnormally necrotic digit-joint region', 0.4788732394366197, 6.466375519622663, 1.7597085532824348, 'UPHENO:0086700', 'abnormal digit morphology'),
(32398, 'HP:0010338', 'Deviation of the 4th toe', 'XPO:0102566', 'abnormal claw primordium morphology', 0.525, 7.639349617137506, 2.002662864537412, 'UPHENO:0088132', 'abnormal pedal digit morphology'),
(32399, 'HP:0010338', 'Deviation of the 4th toe', 'XPO:0133379', 'fused hindlimb digits part of regenerating hindlimb', 0.4329896907216495, 7.639349617137506, 1.8187247257457408, 'HP:0001780', 'Abnormal toe morphology'),
(32400, 'HP:0010338', 'Deviation of the 4th toe', 'XPO:0130797', 'increased size of the hindlimb digit 4', 0.44680851063829785, 7.639349617137506, 1.8475189916962858, 'UPHENO:0088132', 'abnormal pedal digit morphology'),
(32401, 'HP:0010338', 'Deviation of the 4th toe', 'XPO:0128497', 'decreased size of the digit-joint region', 0.4657534246575342, 6.466375519622663, 1.7354355486119033, 'UPHENO:0086700', 'abnormal digit morphology'),
(32402, 'HP:0010338', 'Deviation of the 4th toe', 'XPO:0141558', 'abnormal claw morphology in the regenerating hindlimb', 0.4077669902912621, 7.639349617137506, 1.7649573935828782, 'UPHENO:0088132', 'abnormal pedal digit morphology'),
(32403, 'HP:0010338', 'Deviation of the 4th toe', 'XPO:0140234', 'abnormally necrotic hindlimb digit 5', 0.45652173913043476, 7.639349617137506, 1.8674927504654564, 'UPHENO:0088132', 'abnormal pedal digit morphology'),
(32404, 'HP:0010338', 'Deviation of the 4th toe', 'XPO:0129693', 'increased size of the digit', 0.4473684210526316, 6.466375519622663, 1.7008386772845274, 'UPHENO:0086700', 'abnormal digit morphology'),
(32405, 'HP:0010338', 'Deviation of the 4th toe', 'XPO:0129931', 'increased size of the hindlimb digit 5', 0.44680851063829785, 7.639349617137506, 1.8475189916962858, 'UPHENO:0088132', 'abnormal pedal digit morphology'),
(32406, 'HP:0010338', 'Deviation of the 4th toe', 'XPO:0141547', 'abnormal hindlimb digit morphology in the regenerating hindlimb', 0.4827586206896552, 7.639349617137506, 1.920406697586568, 'UPHENO:0088132', 'abnormal pedal digit morphology'),
(32407, 'HP:0010338', 'Deviation of the 4th toe', 'XPO:0140514', 'abnormally necrotic hindlimb digit 4', 0.45652173913043476, 7.639349617137506, 1.8674927504654564, 'UPHENO:0088132', 'abnormal pedal digit morphology'),
(32408, 'HP:0010338', 'Deviation of the 4th toe', 'XPO:0102927', 'abnormal claw of hindlimb digit 1 morphology', 0.42, 7.639349617137506, 1.791236120448042, 'HP:0001780', 'Abnormal toe morphology'),
(32409, 'HP:0010338', 'Deviation of the 4th toe', 'XPO:0139922', 'abnormally necrotic claw', 0.4117647058823529, 7.639349617137506, 1.773588043552699, 'UPHENO:0088132', 'abnormal pedal digit morphology'),
(32410, 'HP:0010338', 'Deviation of the 4th toe', 'XPO:0126603', 'abnormally localised digit', 0.4027777777777778, 6.393467666143939, 1.6047263626124957, 'HP:0011297', 'Abnormal digit morphology'),
(32411, 'HP:0010338', 'Deviation of the 4th toe', 'XPO:0101809', 'abnormal hindlimb digit morphology', 0.5185185185185185, 7.639349617137506, 1.9902623560533799, 'UPHENO:0088132', 'abnormal pedal digit morphology'),
(32412, 'HP:0010338', 'Deviation of the 4th toe', 'XPO:0101872', 'abnormal hindlimb digit 1 morphology', 0.5060240963855421, 7.639349617137506, 1.9661370722778317, 'UPHENO:0088132', 'abnormal pedal digit morphology'),
(32413, 'HP:0010338', 'Deviation of the 4th toe', 'XPO:0103462', 'bifurcated hindlimb digit 3', 0.42424242424242425, 7.639349617137506, 1.800260037108487, 'UPHENO:0088132', 'abnormal pedal digit morphology'),
(32414, 'HP:0010338', 'Deviation of the 4th toe', 'XPO:0102880', 'abnormal digit-joint region morphology', 0.5074626865671642, 6.466375519622663, 1.8114757225919036, 'UPHENO:0086700', 'abnormal digit morphology'),
(32415, 'HP:0010338', 'Deviation of the 4th toe', 'XPO:0103759', 'increased size of the hindlimb digit', 0.46153846153846156, 7.639349617137506, 1.877725664054278, 'HP:0001780', 'Abnormal toe morphology'),
(32416, 'HP:0010338', 'Deviation of the 4th toe', 'XPO:0129752', 'increased size of the hindlimb digit 2', 0.44680851063829785, 7.639349617137506, 1.8475189916962858, 'HP:0001780', 'Abnormal toe morphology'),
(32417, 'HP:0010338', 'Deviation of the 4th toe', 'XPO:0140680', 'abnormally necrotic hindlimb digit 3', 0.45652173913043476, 7.639349617137506, 1.8674927504654564, 'UPHENO:0088132', 'abnormal pedal digit morphology'),
(32418, 'HP:0010338', 'Deviation of the 4th toe', 'XPO:0101248', 'abnormal digit-joint region', 0.4375, 6.393467666143939, 1.6724658752686028, 'UPHENO:0002905', 'abnormal digit'),
(32419, 'HP:0010338', 'Deviation of the 4th toe', 'XPO:0139924', 'abnormally necrotic hindlimb digit 1', 0.45652173913043476, 7.639349617137506, 1.8674927504654564, 'HP:0001780', 'Abnormal toe morphology'),
(32420, 'HP:0010338', 'Deviation of the 4th toe', 'XPO:0128213', 'decreased size of the digit', 0.4473684210526316, 6.466375519622663, 1.7008386772845274, 'UPHENO:0086700', 'abnormal digit morphology'),
(32421, 'HP:0010338', 'Deviation of the 4th toe', 'XPO:0128670', 'decreased size of the claw primordium', 0.4827586206896552, 7.639349617137506, 1.920406697586568, 'HP:0001780', 'Abnormal toe morphology'),
(32422, 'HP:0010338', 'Deviation of the 4th toe', 'XPO:0102797', 'abnormal claw of hindlimb digit 3 morphology', 0.42, 7.639349617137506, 1.791236120448042, 'UPHENO:0088132', 'abnormal pedal digit morphology'),
(32423, 'HP:0010338', 'Deviation of the 4th toe', 'XPO:0127078', 'abnormally localised digit-joint region', 0.4084507042253521, 6.393467666143939, 1.6159877384059913, 'UPHENO:0002905', 'abnormal digit'),
(32424, 'HP:0010338', 'Deviation of the 4th toe', 'XPO:0103460', 'bifurcated hindlimb digit 1', 0.42424242424242425, 7.639349617137506, 1.800260037108487, 'HP:0001780', 'Abnormal toe morphology'),
(32425, 'HP:0010338', 'Deviation of the 4th toe', 'XPO:0129977', 'increased size of the digit-joint region', 0.4657534246575342, 6.466375519622663, 1.7354355486119033, 'UPHENO:0086700', 'abnormal digit morphology'),
(32426, 'HP:0010338', 'Deviation of the 4th toe', 'XPO:0101810', 'abnormal digit morphology', 0.5074626865671642, 6.466375519622663, 1.8114757225919036, 'UPHENO:0086700', 'abnormal digit morphology'),
(32427, 'HP:0010338', 'Deviation of the 4th toe', 'XPO:0129648', 'increased size of the hindlimb digit 1', 0.44680851063829785, 7.639349617137506, 1.8475189916962858, 'UPHENO:0088132', 'abnormal pedal digit morphology'),
(32428, 'HP:0010338', 'Deviation of the 4th toe', 'XPO:0128166', 'decreased size of the claw', 0.40384615384615385, 7.639349617137506, 1.7564515253109234, 'HP:0001780', 'Abnormal toe morphology'),
(32429, 'HP:0010338', 'Deviation of the 4th toe', 'XPO:0103191', 'abnormal claw of hindlimb digit 5 morphology', 0.42, 7.639349617137506, 1.791236120448042, 'UPHENO:0088132', 'abnormal pedal digit morphology'),
(32430, 'HP:0010338', 'Deviation of the 4th toe', 'XPO:0102457', 'abnormal claw of hindlimb digit 2 morphology', 0.42, 7.639349617137506, 1.791236120448042, 'UPHENO:0088132', 'abnormal pedal digit morphology'),
(32431, 'HP:0010338', 'Deviation of the 4th toe', 'XPO:0128272', 'decreased size of the hindlimb digit 2', 0.44680851063829785, 7.639349617137506, 1.8475189916962858, 'UPHENO:0088132', 'abnormal pedal digit morphology'),
(32432, 'HP:0010338', 'Deviation of the 4th toe', 'XPO:0128802', 'decreased size of the hindlimb digit 3', 0.44680851063829785, 7.639349617137506, 1.8475189916962858, 'UPHENO:0088132', 'abnormal pedal digit morphology'),
(32433, 'HP:0010338', 'Deviation of the 4th toe', 'XPO:0100178', 'abnormal digit', 0.45901639344262296, 6.393467666143939, 1.7130984997090548, 'UPHENO:0002905', 'abnormal digit'),
(32434, 'HP:0010338', 'Deviation of the 4th toe', 'XPO:0141569', 'abnormal digit-joint region morphology in the regenerating hindlimb', 0.4657534246575342, 6.466375519622663, 1.7354355486119033, 'UPHENO:0086700', 'abnormal digit morphology'),
(32435, 'HP:0010338', 'Deviation of the 4th toe', 'XPO:0139961', 'abnormally necrotic hindlimb digit', 0.47191011235955055, 7.639349617137506, 1.8987064902657413, 'HP:0001780', 'Abnormal toe morphology'),
(32436, 'HP:0010338', 'Deviation of the 4th toe', 'XPO:0128451', 'decreased size of the hindlimb digit 5', 0.44680851063829785, 7.639349617137506, 1.8475189916962858, 'HP:0001780', 'Abnormal toe morphology'),
(32437, 'HP:0010338', 'Deviation of the 4th toe', 'XPO:0103044', 'abnormal claw of hindlimb digit 4 morphology', 0.42, 7.639349617137506, 1.791236120448042, 'HP:0001780', 'Abnormal toe morphology'),
(32438, 'HP:0010338', 'Deviation of the 4th toe', 'XPO:0103463', 'bifurcated hindlimb digit 4', 0.42424242424242425, 7.639349617137506, 1.800260037108487, 'UPHENO:0088132', 'abnormal pedal digit morphology'),
(32439, 'HP:0010338', 'Deviation of the 4th toe', 'XPO:0141568', 'abnormal digit-joint region morphology in the regenerating forelimb', 0.4657534246575342, 6.466375519622663, 1.7354355486119033, 'UPHENO:0086700', 'abnormal digit morphology'),
(32440, 'HP:0010338', 'Deviation of the 4th toe', 'XPO:0101869', 'abnormal claw morphology', 0.4329896907216495, 7.639349617137506, 1.8187247257457408, 'UPHENO:0088132', 'abnormal pedal digit morphology'),
(32441, 'HP:0010338', 'Deviation of the 4th toe', 'XPO:0140474', 'abnormally necrotic hindlimb digit 2', 0.45652173913043476, 7.639349617137506, 1.8674927504654564, 'UPHENO:0088132', 'abnormal pedal digit morphology'),
(32442, 'HP:0010338', 'Deviation of the 4th toe', 'XPO:0130280', 'increased size of the hindlimb digit 3', 0.44680851063829785, 7.639349617137506, 1.8475189916962858, 'UPHENO:0088132', 'abnormal pedal digit morphology'),
(32443, 'HP:0010338', 'Deviation of the 4th toe', 'XPO:0102180', 'abnormal hindlimb digit 3 morphology', 0.5060240963855421, 7.639349617137506, 1.9661370722778317, 'UPHENO:0088132', 'abnormal pedal digit morphology'),
(32444, 'HP:0010338', 'Deviation of the 4th toe', 'XPO:0129321', 'decreased size of the hindlimb digit 4', 0.44680851063829785, 7.639349617137506, 1.8475189916962858, 'HP:0001780', 'Abnormal toe morphology'),
(32445, 'HP:0010338', 'Deviation of the 4th toe', 'XPO:0103632', 'abnormally increased number of digit', 0.4027777777777778, 6.393467666143939, 1.6047263626124957, 'UPHENO:0002905', 'abnormal digit'),
(32446, 'HP:0010338', 'Deviation of the 4th toe', 'XPO:0128168', 'decreased size of the hindlimb digit 1', 0.44680851063829785, 7.639349617137506, 1.8475189916962858, 'UPHENO:0088132', 'abnormal pedal digit morphology'),
(32447, 'HP:0010338', 'Deviation of the 4th toe', 'XPO:0130149', 'increased size of the claw primordium', 0.4827586206896552, 7.639349617137506, 1.920406697586568, 'UPHENO:0088132', 'abnormal pedal digit morphology'),
(32448, 'HP:0010338', 'Deviation of the 4th toe', 'XPO:0129646', 'increased size of the claw', 0.40384615384615385, 7.639349617137506, 1.7564515253109234, 'UPHENO:0088132', 'abnormal pedal digit morphology'),
(32449, 'HP:0010338', 'Deviation of the 4th toe', 'XPO:0133357', 'fused hindlimb digits', 0.4666666666666667, 7.639349617137506, 1.8881286559265065, 'HP:0001780', 'Abnormal toe morphology'),
(32450, 'HP:0010338', 'Deviation of the 4th toe', 'XPO:0139979', 'abnormally necrotic claw primordium', 0.49411764705882355, 7.639349617137506, 1.9428683583505366, 'HP:0001780', 'Abnormal toe morphology'),
(32451, 'HP:0010338', 'Deviation of the 4th toe', 'XPO:0102051', 'abnormal hindlimb digit 2 morphology', 0.5060240963855421, 7.639349617137506, 1.9661370722778317, 'UPHENO:0088132', 'abnormal pedal digit morphology'),
(32452, 'HP:0010338', 'Deviation of the 4th toe', 'XPO:0103464', 'bifurcated hindlimb digit 5', 0.42424242424242425, 7.639349617137506, 1.800260037108487, 'UPHENO:0088132', 'abnormal pedal digit morphology'),
(32453, 'HP:0010338', 'Deviation of the 4th toe', 'XPO:0102876', 'abnormal hindlimb digit 4 morphology', 0.5060240963855421, 7.639349617137506, 1.9661370722778317, 'UPHENO:0088132', 'abnormal pedal digit morphology'),
(32454, 'HP:0010338', 'Deviation of the 4th toe', 'XPO:0103436', 'decreased size of the hindlimb digit', 0.46153846153846156, 7.639349617137506, 1.877725664054278, 'HP:0001780', 'Abnormal toe morphology'),
(32455, 'HP:0012798', 'Pulmonary lymphangiomyomatosis', 'XPO:0140932', 'abnormally necrotic ventral caudal lymphatic vessel', 0.4246575342465753, 12.404694921567193, 2.2951573276082273, 'UPHENO:0020778', 'abnormal lymphatic vessel morphology'),
(32456, 'HP:0012798', 'Pulmonary lymphangiomyomatosis', 'XPO:0100210', 'abnormal pulmonary artery', 0.43661971830985913, 9.627087342903641, 2.050213687351394, 'UPHENO:0019970', 'abnormal lung morphology'),
(32457, 'HP:0012798', 'Pulmonary lymphangiomyomatosis', 'XPO:0128964', 'decreased size of the dorsal caudal lymphatic vessel', 0.40789473684210525, 12.404694921567193, 2.24940209181001, 'UPHENO:0020778', 'abnormal lymphatic vessel morphology'),
(32458, 'HP:0012798', 'Pulmonary lymphangiomyomatosis', 'XPO:0103180', 'abnormal pulmonary vein morphology', 0.40229885057471265, 9.627087342903641, 1.967985307981871, 'UPHENO:0019970', 'abnormal lung morphology'),
(32459, 'HP:0012798', 'Pulmonary lymphangiomyomatosis', 'XPO:0102553', 'abnormal dorsal caudal lymphatic vessel morphology', 0.4626865671641791, 12.404694921567193, 2.395722377484263, 'HP:0100766', 'Abnormal lymphatic vessel morphology'),
(32460, 'HP:0012798', 'Pulmonary lymphangiomyomatosis', 'XPO:0130463', 'increased size of the ventral caudal lymphatic vessel', 0.40789473684210525, 12.404694921567193, 2.24940209181001, 'HP:0100766', 'Abnormal lymphatic vessel morphology'),
(32461, 'HP:0012798', 'Pulmonary lymphangiomyomatosis', 'XPO:0128986', 'decreased size of the ventral caudal lymphatic vessel', 0.40789473684210525, 12.404694921567193, 2.24940209181001, 'UPHENO:0020778', 'abnormal lymphatic vessel morphology'),
(32462, 'HP:0012798', 'Pulmonary lymphangiomyomatosis', 'XPO:0140735', 'abnormally necrotic lymph vessel', 0.44285714285714284, 12.404694921567193, 2.343823319062202, 'HP:0100766', 'Abnormal lymphatic vessel morphology'),
(32463, 'HP:0012798', 'Pulmonary lymphangiomyomatosis', 'XPO:0128271', 'decreased size of the lymph vessel', 0.4246575342465753, 12.404694921567193, 2.2951573276082273, 'HP:0100766', 'Abnormal lymphatic vessel morphology'),
(32464, 'HP:0012798', 'Pulmonary lymphangiomyomatosis', 'XPO:0101548', 'abnormal pulmonary vein', 0.43661971830985913, 9.627087342903641, 2.050213687351394, 'HP:0002088', 'Abnormal lung morphology'),
(32465, 'HP:0012798', 'Pulmonary lymphangiomyomatosis', 'XPO:0129751', 'increased size of the lymph vessel', 0.4246575342465753, 12.404694921567193, 2.2951573276082273, 'UPHENO:0020778', 'abnormal lymphatic vessel morphology'),
(32466, 'HP:0012798', 'Pulmonary lymphangiomyomatosis', 'XPO:0130442', 'increased size of the dorsal caudal lymphatic vessel', 0.40789473684210525, 12.404694921567193, 2.24940209181001, 'HP:0100766', 'Abnormal lymphatic vessel morphology'),
(32467, 'HP:0012798', 'Pulmonary lymphangiomyomatosis', 'XPO:0101842', 'abnormal pulmonary artery morphology', 0.4117647058823529, 9.627087342903641, 1.991003462642504, 'HP:0002088', 'Abnormal lung morphology'),
(32468, 'HP:0012798', 'Pulmonary lymphangiomyomatosis', 'XPO:0102645', 'abnormal ventral caudal lymphatic vessel morphology', 0.4626865671641791, 12.404694921567193, 2.395722377484263, 'HP:0100766', 'Abnormal lymphatic vessel morphology'),
(32469, 'HP:0012798', 'Pulmonary lymphangiomyomatosis', 'XPO:0102554', 'abnormal lymph vessel morphology', 0.47692307692307695, 12.404694921567193, 2.432300407080896, 'UPHENO:0020778', 'abnormal lymphatic vessel morphology'),
(32470, 'HP:0012798', 'Pulmonary lymphangiomyomatosis', 'XPO:0100117', 'abnormal aortic arch', 0.40540540540540543, 7.241224942262181, 1.7133685340140727, 'HP:0012252', 'Abnormal respiratory system morphology'),
(32471, 'HP:0012798', 'Pulmonary lymphangiomyomatosis', 'XPO:0140894', 'abnormally necrotic dorsal caudal lymphatic vessel', 0.4246575342465753, 12.404694921567193, 2.2951573276082273, 'UPHENO:0020778', 'abnormal lymphatic vessel morphology'),
(32472, 'HP:0034054', 'Probst bundles', 'XPO:0102191', 'abnormal telencephalon morphology', 0.4264705882352941, 8.02346099791745, 1.8498027277157947, 'HP:0002060', 'Abnormal cerebral morphology'),
(32473, 'HP:0034054', 'Probst bundles', 'XPO:0129372', 'decreased size of the anterior entopeduncular region', 0.4027777777777778, 8.02346099791745, 1.7976851200440698, 'HP:0002060', 'Abnormal cerebral morphology'),
(32474, 'HP:0034054', 'Probst bundles', 'XPO:0101970', 'abnormal lateral ganglionic eminence morphology', 0.4084507042253521, 8.02346099791745, 1.810300608993995, 'HP:0002060', 'Abnormal cerebral morphology'),
(32475, 'HP:0034054', 'Probst bundles', 'XPO:0101805', 'abnormal pallidum morphology', 0.4027777777777778, 8.02346099791745, 1.7976851200440698, 'HP:0002060', 'Abnormal cerebral morphology'),
(32476, 'HP:0034054', 'Probst bundles', 'XPO:0100195', 'abnormal retromammillary area', 0.4090909090909091, 6.667568321314008, 1.6515573214369805, 'HP:0100547', 'Abnormal forebrain morphology'),
(32477, 'HP:0034054', 'Probst bundles', 'XPO:0142058', 'abnormal cerebrospinal fluid morphology', 0.40384615384615385, 5.483278994082134, 1.4880863994491305, 'HP:0002011', 'Morphological central nervous system abnormality'),
(32478, 'HP:0034054', 'Probst bundles', 'XPO:0100194', 'abnormal preoptic area', 0.40298507462686567, 6.667568321314008, 1.639185931352649, 'HP:0100547', 'Abnormal forebrain morphology'),
(32479, 'HP:0034054', 'Probst bundles', 'XPO:0102442', 'abnormal medial pallium morphology', 0.4142857142857143, 8.02346099791745, 1.8231854734408677, 'HP:0002060', 'Abnormal cerebral morphology'),
(32480, 'HP:0034054', 'Probst bundles', 'XPO:0101123', 'abnormal third ventricle', 0.40298507462686567, 6.667568321314008, 1.639185931352649, 'HP:0100547', 'Abnormal forebrain morphology'),
(32481, 'HP:0034054', 'Probst bundles', 'XPO:0101851', 'abnormal basal ganglion morphology', 0.4084507042253521, 8.02346099791745, 1.810300608993995, 'HP:0002060', 'Abnormal cerebral morphology'),
(32482, 'HP:0034054', 'Probst bundles', 'XPO:0100698', 'abnormal optic stalk', 0.40298507462686567, 6.667568321314008, 1.639185931352649, 'HP:0100547', 'Abnormal forebrain morphology'),
(32483, 'HP:0034054', 'Probst bundles', 'XPO:0101053', 'abnormal anterior hypothalamus', 0.4090909090909091, 6.667568321314008, 1.6515573214369805, 'HP:0100547', 'Abnormal forebrain morphology'),
(32484, 'HP:0034054', 'Probst bundles', 'XPO:0100263', 'abnormal prethalamus', 0.4090909090909091, 6.667568321314008, 1.6515573214369805, 'HP:0100547', 'Abnormal forebrain morphology'),
(32485, 'HP:0034054', 'Probst bundles', 'XPO:0101117', 'abnormal tuberal region', 0.40298507462686567, 6.667568321314008, 1.639185931352649, 'HP:0100547', 'Abnormal forebrain morphology'),
(32486, 'HP:0034054', 'Probst bundles', 'XPO:0101354', 'abnormal eminentia thalami', 0.4153846153846154, 6.667568321314008, 1.6642131181731699, 'HP:0100547', 'Abnormal forebrain morphology'),
(32487, 'HP:0034054', 'Probst bundles', 'XPO:0102249', 'abnormal forebrain morphology', 0.40298507462686567, 6.667568321314008, 1.639185931352649, 'HP:0100547', 'Abnormal forebrain morphology'),
(32488, 'HP:0034054', 'Probst bundles', 'XPO:0101526', 'abnormal infundibulum', 0.40298507462686567, 6.667568321314008, 1.639185931352649, 'HP:0100547', 'Abnormal forebrain morphology'),
(32489, 'HP:0034054', 'Probst bundles', 'XPO:0100763', 'abnormal pretectum', 0.4153846153846154, 6.667568321314008, 1.6642131181731699, 'HP:0100547', 'Abnormal forebrain morphology'),
(32490, 'HP:0034054', 'Probst bundles', 'XPO:0102357', 'abnormal subpallium morphology', 0.42028985507246375, 8.02346099791745, 1.8363494384224073, 'HP:0002060', 'Abnormal cerebral morphology'),
(32491, 'HP:0034054', 'Probst bundles', 'XPO:0107380', 'abnormal dorsal telencephalon morphology', 0.42028985507246375, 8.02346099791745, 1.8363494384224073, 'HP:0002060', 'Abnormal cerebral morphology'),
(32492, 'HP:0034054', 'Probst bundles', 'XPO:0100695', 'abnormal zona limitans intrathalamica', 0.4090909090909091, 6.667568321314008, 1.6515573214369805, 'HP:0100547', 'Abnormal forebrain morphology'),
(32493, 'HP:0034054', 'Probst bundles', 'XPO:0100962', 'abnormal dorsal thalamus', 0.4090909090909091, 6.667568321314008, 1.6515573214369805, 'HP:0100547', 'Abnormal forebrain morphology'),
(32494, 'HP:0034054', 'Probst bundles', 'XPO:0101186', 'abnormal optic chiasm', 0.4153846153846154, 6.667568321314008, 1.6642131181731699, 'HP:0100547', 'Abnormal forebrain morphology'),
(32495, 'HP:0034054', 'Probst bundles', 'XPO:0140421', 'abnormally necrotic anterior entopeduncular region', 0.4142857142857143, 8.02346099791745, 1.8231854734408677, 'HP:0002060', 'Abnormal cerebral morphology'),
(32496, 'HP:0034054', 'Probst bundles', 'XPO:0101293', 'abnormal posterior hypothalamus', 0.4090909090909091, 6.667568321314008, 1.6515573214369805, 'HP:0100547', 'Abnormal forebrain morphology'),
(32497, 'HP:0034054', 'Probst bundles', 'XPO:0103178', 'abnormal dorsal pallium morphology', 0.4142857142857143, 8.02346099791745, 1.8231854734408677, 'HP:0002060', 'Abnormal cerebral morphology'),
(32498, 'HP:0034054', 'Probst bundles', 'XPO:0102826', 'abnormal anterior commissure morphology', 0.4142857142857143, 8.02346099791745, 1.8231854734408677, 'HP:0002060', 'Abnormal cerebral morphology'),
(32499, 'HP:0034054', 'Probst bundles', 'XPO:0101595', 'abnormal prosomere 4', 0.40298507462686567, 6.667568321314008, 1.639185931352649, 'HP:0100547', 'Abnormal forebrain morphology'),
(32500, 'HP:0034054', 'Probst bundles', 'XPO:0100157', 'abnormal optic tract', 0.4153846153846154, 6.667568321314008, 1.6642131181731699, 'HP:0100547', 'Abnormal forebrain morphology'),
(32501, 'HP:0034054', 'Probst bundles', 'XPO:0101987', 'abnormal striatum morphology', 0.4027777777777778, 8.02346099791745, 1.7976851200440698, 'HP:0002060', 'Abnormal cerebral morphology'),
(32502, 'HP:0034054', 'Probst bundles', 'XPO:0102174', 'abnormal pallium morphology', 0.42028985507246375, 8.02346099791745, 1.8363494384224073, 'HP:0002060', 'Abnormal cerebral morphology'),
(32503, 'HP:0034054', 'Probst bundles', 'XPO:0101496', 'abnormal subcommissural organ', 0.4090909090909091, 6.667568321314008, 1.6515573214369805, 'HP:0100547', 'Abnormal forebrain morphology'),
(32504, 'HP:0034054', 'Probst bundles', 'XPO:0101986', 'abnormal amygdala morphology', 0.4084507042253521, 8.02346099791745, 1.810300608993995, 'HP:0002060', 'Abnormal cerebral morphology'),
(32505, 'HP:0034054', 'Probst bundles', 'XPO:0130846', 'increased size of the anterior entopeduncular region', 0.4027777777777778, 8.02346099791745, 1.7976851200440698, 'HP:0002060', 'Abnormal cerebral morphology'),
(32506, 'HP:0034054', 'Probst bundles', 'XPO:0102007', 'abnormal anterior entopeduncular region morphology', 0.43283582089552236, 8.02346099791745, 1.8635560972122107, 'HP:0002060', 'Abnormal cerebral morphology'),
(32507, 'HP:0034054', 'Probst bundles', 'XPO:0101075', 'abnormal mammilary region', 0.40298507462686567, 6.667568321314008, 1.639185931352649, 'HP:0100547', 'Abnormal forebrain morphology'),
(32508, 'HP:0034054', 'Probst bundles', 'XPO:0102066', 'abnormal ventral pallium morphology', 0.4142857142857143, 8.02346099791745, 1.8231854734408677, 'HP:0002060', 'Abnormal cerebral morphology'),
(32509, 'HP:0034054', 'Probst bundles', 'XPO:0100590', 'abnormal hypothalamus', 0.4153846153846154, 6.667568321314008, 1.6642131181731699, 'HP:0100547', 'Abnormal forebrain morphology'),
(32510, 'HP:0034054', 'Probst bundles', 'XPO:0100729', 'abnormal thalamus', 0.4153846153846154, 6.667568321314008, 1.6642131181731699, 'HP:0100547', 'Abnormal forebrain morphology'),
(32511, 'HP:0034054', 'Probst bundles', 'XPO:0100611', 'abnormal hypophysis', 0.40298507462686567, 6.667568321314008, 1.639185931352649, 'HP:0100547', 'Abnormal forebrain morphology'),
(32512, 'HP:0034054', 'Probst bundles', 'XPO:0102968', 'abnormal medial ganglionic eminence morphology', 0.4084507042253521, 8.02346099791745, 1.810300608993995, 'HP:0002060', 'Abnormal cerebral morphology'),
(32513, 'HP:0034054', 'Probst bundles', 'XPO:0101797', 'abnormal lateral pallium morphology', 0.4142857142857143, 8.02346099791745, 1.8231854734408677, 'HP:0002060', 'Abnormal cerebral morphology'),
(32514, 'HP:0034054', 'Probst bundles', 'XPO:0102238', 'abnormal basal forebrain morphology', 0.42028985507246375, 8.02346099791745, 1.8363494384224073, 'HP:0002060', 'Abnormal cerebral morphology'),
(32515, 'HP:0034054', 'Probst bundles', 'XPO:0100575', 'abnormal diencephalon', 0.421875, 6.667568321314008, 1.677164388351466, 'HP:0100547', 'Abnormal forebrain morphology'),
(32516, 'HP:0034054', 'Probst bundles', 'XPO:0100988', 'abnormal habenula', 0.40298507462686567, 6.667568321314008, 1.639185931352649, 'HP:0100547', 'Abnormal forebrain morphology'),
(32517, 'HP:0011830', 'Abnormal oral mucosa morphology', 'XPO:0102367', 'abnormal hindgut morphology', 0.4117647058823529, 5.725717590856133, 1.5354635846428564, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(32518, 'HP:0011830', 'Abnormal oral mucosa morphology', 'XPO:0140086', 'abnormally necrotic branchial arch 4', 0.4090909090909091, 5.725717590856133, 1.5304701939081158, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(32519, 'HP:0011830', 'Abnormal oral mucosa morphology', 'XPO:0103324', 'decreased size of the branchial arch', 0.4153846153846154, 5.725717590856133, 1.5421981063659433, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(32520, 'HP:0011830', 'Abnormal oral mucosa morphology', 'XPO:0102753', 'abnormal Rathkes pouch morphology', 0.4153846153846154, 5.725717590856133, 1.5421981063659433, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(32521, 'HP:0011830', 'Abnormal oral mucosa morphology', 'XPO:0103358', 'decreased size of the pharyngeal region', 0.40384615384615385, 4.5318002188002176, 1.3528303989641963, 'UPHENO:0087907', 'abnormal head morphology'),
(32522, 'HP:0011830', 'Abnormal oral mucosa morphology', 'XPO:0128105', 'decreased size of the tongue', 0.5223880597014925, 7.884497199543557, 2.0294746102849897, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(32523, 'HP:0011830', 'Abnormal oral mucosa morphology', 'XPO:0102082', 'abnormal circumpharyngeal ridge morphology', 0.40384615384615385, 4.5318002188002176, 1.3528303989641963, 'UPHENO:0087907', 'abnormal head morphology'),
(32524, 'HP:0011830', 'Abnormal oral mucosa morphology', 'XPO:0140440', 'abnormally necrotic branchial arch 3', 0.4153846153846154, 5.725717590856133, 1.5421981063659433, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(32525, 'HP:0011830', 'Abnormal oral mucosa morphology', 'XPO:0130132', 'increased size of the oral epithelium', 0.4788732394366197, 11.317232080316854, 2.327986165714343, 'UPHENO:0087132', 'abnormal mouth mucosa morphology'),
(32526, 'HP:0011830', 'Abnormal oral mucosa morphology', 'XPO:0101788', 'abnormal foregut morphology', 0.4117647058823529, 5.725717590856133, 1.5354635846428564, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(32527, 'HP:0011830', 'Abnormal oral mucosa morphology', 'XPO:0140430', 'abnormally necrotic hyoid arch', 0.42857142857142855, 5.725717590856133, 1.5664861849086864, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(32528, 'HP:0011830', 'Abnormal oral mucosa morphology', 'XPO:0129152', 'decreased size of the oral cavity', 0.5932203389830508, 7.884497199543557, 2.16269371419629, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(32529, 'HP:0011830', 'Abnormal oral mucosa morphology', 'XPO:0102204', 'abnormal branchial arch morphology', 0.48214285714285715, 5.725717590856133, 1.6615095059759644, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(32530, 'HP:0011830', 'Abnormal oral mucosa morphology', 'XPO:0102861', 'abnormal cementum morphology', 0.4268292682926829, 7.884497199543557, 1.8344847152639032, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(32531, 'HP:0011830', 'Abnormal oral mucosa morphology', 'XPO:0140335', 'abnormally necrotic pharyngeal region', 0.42, 4.5318002188002176, 1.3796217205799897, 'UPHENO:0087907', 'abnormal head morphology'),
(32532, 'HP:0011830', 'Abnormal oral mucosa morphology', 'XPO:0140897', 'abnormally necrotic lower jaw', 0.44594594594594594, 7.312692920701687, 1.8058421198805104, 'UPHENO:0076800', 'abnormal mouth morphology'),
(32533, 'HP:0011830', 'Abnormal oral mucosa morphology', 'XPO:0141311', 'abnormal roof of mouth morphology', 0.5789473684210527, 7.312692920701687, 2.0575870145662134, 'UPHENO:0076800', 'abnormal mouth morphology'),
(32534, 'HP:0011830', 'Abnormal oral mucosa morphology', 'XPO:0142061', 'abnormal digestive tract morphology', 0.42857142857142855, 5.725717590856133, 1.5664861849086864, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(32535, 'HP:0011830', 'Abnormal oral mucosa morphology', 'XPO:0102960', 'abnormal oral epithelium morphology', 0.5483870967741935, 11.317232080316854, 2.491229424209004, 'UPHENO:0087132', 'abnormal mouth mucosa morphology'),
(32536, 'HP:0011830', 'Abnormal oral mucosa morphology', 'XPO:0129585', 'increased size of the tongue', 0.4861111111111111, 7.884497199543557, 1.9577389239177327, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(32537, 'HP:0011830', 'Abnormal oral mucosa morphology', 'XPO:0140386', 'abnormally necrotic pharyngeal mesenchyme', 0.4090909090909091, 5.725717590856133, 1.5304701939081158, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(32538, 'HP:0011830', 'Abnormal oral mucosa morphology', 'XPO:0102522', 'abnormal pharyngeal cavity morphology', 0.44680851063829785, 5.725717590856133, 1.5994684583029237, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(32539, 'HP:0011830', 'Abnormal oral mucosa morphology', 'XPO:0102223', 'abnormal pharyngeal arch morphology', 0.5, 5.725717590856133, 1.6919984620052309, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(32540, 'HP:0011830', 'Abnormal oral mucosa morphology', 'XPO:0126089', 'absent tongue', 0.55, 7.884497199543557, 2.0824200968462048, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(32541, 'HP:0011830', 'Abnormal oral mucosa morphology', 'XPO:0101816', 'abnormal tooth morphology', 0.4794520547945205, 7.884497199543557, 1.9442835141364547, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(32542, 'HP:0011830', 'Abnormal oral mucosa morphology', 'XPO:0140283', 'abnormally necrotic branchial arch 2', 0.4090909090909091, 5.725717590856133, 1.5304701939081158, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(32543, 'HP:0011830', 'Abnormal oral mucosa morphology', 'XPO:0115392', 'abnormally incomplete structure of alimentary system', 0.4375, 5.725717590856133, 1.582719635943005, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(32544, 'HP:0011830', 'Abnormal oral mucosa morphology', 'XPO:0102420', 'abnormal branchial arch 4 morphology', 0.4576271186440678, 5.725717590856133, 1.6187166655326515, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(32545, 'HP:0011830', 'Abnormal oral mucosa morphology', 'XPO:0101567', 'abnormal tongue', 0.6666666666666666, 7.884497199543557, 2.292669070398598, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(32546, 'HP:0011830', 'Abnormal oral mucosa morphology', 'XPO:0141830', 'increased width of mouth', 0.5147058823529411, 7.884497199543557, 2.0144967331818533, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(32547, 'HP:0011830', 'Abnormal oral mucosa morphology', 'XPO:0140789', 'abnormally necrotic roof of mouth', 0.532258064516129, 7.312692920701687, 1.9728760174865216, 'UPHENO:0076800', 'abnormal mouth morphology'),
(32548, 'HP:0011830', 'Abnormal oral mucosa morphology', 'XPO:0102618', 'abnormal gut epithelium morphology', 0.40384615384615385, 5.725717590856133, 1.520627839767678, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(32549, 'HP:0011830', 'Abnormal oral mucosa morphology', 'XPO:0141339', 'decreased pigmentation in the head', 0.4117647058823529, 4.5318002188002176, 1.3660290568695288, 'UPHENO:0087907', 'abnormal head morphology'),
(32550, 'HP:0011830', 'Abnormal oral mucosa morphology', 'XPO:0141298', 'abnormal intercanthal region morphology', 0.42, 4.5318002188002176, 1.3796217205799897, 'UPHENO:0087907', 'abnormal head morphology'),
(32551, 'HP:0011830', 'Abnormal oral mucosa morphology', 'XPO:0140700', 'abnormally necrotic branchial arch 1', 0.4090909090909091, 5.725717590856133, 1.5304701939081158, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(32552, 'HP:0011830', 'Abnormal oral mucosa morphology', 'XPO:0142059', 'abnormal nasal region morphology', 0.42857142857142855, 4.5318002188002176, 1.3936283915633758, 'UPHENO:0087907', 'abnormal head morphology'),
(32553, 'HP:0011830', 'Abnormal oral mucosa morphology', 'XPO:0139736', 'abnormally necrotic tooth', 0.43209876543209874, 7.884497199543557, 1.8457739585267778, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(32554, 'HP:0011830', 'Abnormal oral mucosa morphology', 'XPO:0130628', 'increased size of the oral cavity', 0.5932203389830508, 7.884497199543557, 2.16269371419629, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(32555, 'HP:0011830', 'Abnormal oral mucosa morphology', 'XPO:0102525', 'abnormal hyoid arch morphology', 0.47368421052631576, 5.725717590856133, 1.6468703703453182, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(32556, 'HP:0011830', 'Abnormal oral mucosa morphology', 'XPO:0130466', 'increased size of the tooth', 0.4117647058823529, 7.884497199543557, 1.8018206543383524, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(32557, 'HP:0011830', 'Abnormal oral mucosa morphology', 'XPO:0103828', 'decreased width of the mouth', 0.5147058823529411, 7.884497199543557, 2.0144967331818533, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(32558, 'HP:0011830', 'Abnormal oral mucosa morphology', 'XPO:0103101', 'abnormal medial nasal prominence morphology', 0.4117647058823529, 4.5318002188002176, 1.3660290568695288, 'UPHENO:0087907', 'abnormal head morphology'),
(32559, 'HP:0011830', 'Abnormal oral mucosa morphology', 'XPO:0139863', 'abnormally necrotic pharyngeal arch', 0.4576271186440678, 5.725717590856133, 1.6187166655326515, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(32560, 'HP:0011830', 'Abnormal oral mucosa morphology', 'XPO:0102259', 'abnormal pharyngeal region morphology', 0.44680851063829785, 4.5318002188002176, 1.422971154406314, 'UPHENO:0087907', 'abnormal head morphology'),
(32561, 'HP:0011830', 'Abnormal oral mucosa morphology', 'XPO:0126954', 'abnormally localised mouth', 0.41379310344827586, 7.0866363731414825, 1.7124255481192892, 'HP:0000153', 'Abnormality of the mouth'),
(32562, 'HP:0011830', 'Abnormal oral mucosa morphology', 'XPO:0115526', 'abnormally incomplete structure of head', 0.42857142857142855, 4.5318002188002176, 1.3936283915633758, 'UPHENO:0087907', 'abnormal head morphology'),
(32563, 'HP:0011830', 'Abnormal oral mucosa morphology', 'XPO:0101959', 'abnormal visceral pouch morphology', 0.40298507462686567, 5.725717590856133, 1.5190058362769763, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(32564, 'HP:0011830', 'Abnormal oral mucosa morphology', 'XPO:0100591', 'abnormal pharyngeal arch', 0.40425531914893614, 5.05060299610679, 1.4288922723864537, 'HP:0025031', 'Abnormality of the digestive system'),
(32565, 'HP:0011830', 'Abnormal oral mucosa morphology', 'XPO:0100420', 'abnormal choana', 0.40350877192982454, 5.0624614801082695, 1.4292472196161619, 'UPHENO:0002910', 'abnormal face'),
(32566, 'HP:0011830', 'Abnormal oral mucosa morphology', 'XPO:0103013', 'abnormal ventral foregut morphology', 0.40384615384615385, 5.725717590856133, 1.520627839767678, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(32567, 'HP:0011830', 'Abnormal oral mucosa morphology', 'XPO:0102125', 'abnormal liver and biliary system morphology', 0.42857142857142855, 5.725717590856133, 1.5664861849086864, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(32568, 'HP:0011830', 'Abnormal oral mucosa morphology', 'XPO:0102538', 'abnormal lateral nasal prominence morphology', 0.4117647058823529, 4.5318002188002176, 1.3660290568695288, 'UPHENO:0087907', 'abnormal head morphology'),
(32569, 'HP:0011830', 'Abnormal oral mucosa morphology', 'XPO:0128880', 'decreased size of the lower jaw', 0.4342105263157895, 7.312692920701687, 1.7819226251113227, 'UPHENO:0076800', 'abnormal mouth morphology'),
(32570, 'HP:0011830', 'Abnormal oral mucosa morphology', 'XPO:0101506', 'abnormal upper jaw', 0.42592592592592593, 7.0866363731414825, 1.7373491758799184, 'HP:0000153', 'Abnormality of the mouth'),
(32571, 'HP:0011830', 'Abnormal oral mucosa morphology', 'XPO:0131573', 'decreased size of the roof of mouth', 0.515625, 7.312692920701687, 1.9418051620172418, 'UPHENO:0076800', 'abnormal mouth morphology'),
(32572, 'HP:0011830', 'Abnormal oral mucosa morphology', 'XPO:0102155', 'abnormal midgut morphology', 0.4117647058823529, 5.725717590856133, 1.5354635846428564, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(32573, 'HP:0011830', 'Abnormal oral mucosa morphology', 'XPO:0101784', 'abnormal alimentary system morphology', 0.44680851063829785, 5.725717590856133, 1.5994684583029237, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(32574, 'HP:0011830', 'Abnormal oral mucosa morphology', 'XPO:0102734', 'abnormal craniofacial region morphology', 0.4117647058823529, 4.5318002188002176, 1.3660290568695288, 'UPHENO:0087907', 'abnormal head morphology'),
(32575, 'HP:0011830', 'Abnormal oral mucosa morphology', 'XPO:0102203', 'abnormal branchial arch 1 morphology', 0.4576271186440678, 5.725717590856133, 1.6187166655326515, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(32576, 'HP:0011830', 'Abnormal oral mucosa morphology', 'XPO:0131611', 'increased size of the roof of mouth', 0.515625, 7.312692920701687, 1.9418051620172418, 'UPHENO:0076800', 'abnormal mouth morphology'),
(32577, 'HP:0011830', 'Abnormal oral mucosa morphology', 'XPO:0141839', 'edematous pharyngeal region', 0.42857142857142855, 4.5318002188002176, 1.3936283915633758, 'UPHENO:0087907', 'abnormal head morphology'),
(32578, 'HP:0011830', 'Abnormal oral mucosa morphology', 'XPO:0102445', 'abnormal branchial arch 3 morphology', 0.46551724137931033, 5.725717590856133, 1.6326114840378705, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(32579, 'HP:0011830', 'Abnormal oral mucosa morphology', 'XPO:0130340', 'increased size of the pharyngeal mesenchyme', 0.4090909090909091, 5.725717590856133, 1.5304701939081158, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(32580, 'HP:0011830', 'Abnormal oral mucosa morphology', 'XPO:0102890', 'abnormal dentine morphology', 0.4166666666666667, 7.884497199543557, 1.812514045870123, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(32581, 'HP:0011830', 'Abnormal oral mucosa morphology', 'XPO:0101659', 'abnormal lower jaw morphology', 0.4782608695652174, 7.312692920701687, 1.8701269676463677, 'UPHENO:0076800', 'abnormal mouth morphology'),
(32582, 'HP:0011830', 'Abnormal oral mucosa morphology', 'XPO:0128862', 'decreased size of the pharyngeal mesenchyme', 0.4090909090909091, 5.725717590856133, 1.5304701939081158, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(32583, 'HP:0011830', 'Abnormal oral mucosa morphology', 'XPO:0102804', 'abnormal pharyngeal pouch morphology', 0.4117647058823529, 4.5318002188002176, 1.3660290568695288, 'UPHENO:0087907', 'abnormal head morphology'),
(32584, 'HP:0011830', 'Abnormal oral mucosa morphology', 'XPO:0130358', 'increased size of the lower jaw', 0.4342105263157895, 7.312692920701687, 1.7819226251113227, 'UPHENO:0076800', 'abnormal mouth morphology'),
(32585, 'HP:0011830', 'Abnormal oral mucosa morphology', 'XPO:0103352', 'decreased size of the mouth', 0.5555555555555556, 7.884497199543557, 2.0929109445861864, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(32586, 'HP:0011830', 'Abnormal oral mucosa morphology', 'XPO:0101483', 'abnormal nostril', 0.41818181818181815, 5.0624614801082695, 1.455001493548063, 'UPHENO:0002910', 'abnormal face'),
(32587, 'HP:0011830', 'Abnormal oral mucosa morphology', 'XPO:0103138', 'abnormal upper jaw morphology', 0.4647887323943662, 7.312692920701687, 1.8435990000545652, 'UPHENO:0076800', 'abnormal mouth morphology'),
(32588, 'HP:0011830', 'Abnormal oral mucosa morphology', 'XPO:0107375', 'abnormal larval alimentary system morphology', 0.42857142857142855, 5.725717590856133, 1.5664861849086864, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(32589, 'HP:0011830', 'Abnormal oral mucosa morphology', 'XPO:0131651', 'abnormal roof of mouth', 0.4339622641509434, 7.0866363731414825, 1.7536626715827954, 'HP:0000153', 'Abnormality of the mouth'),
(32590, 'HP:0011830', 'Abnormal oral mucosa morphology', 'XPO:0140639', 'abnormally necrotic upper jaw', 0.4342105263157895, 7.312692920701687, 1.7819226251113227, 'UPHENO:0076800', 'abnormal mouth morphology'),
(32591, 'HP:0011830', 'Abnormal oral mucosa morphology', 'XPO:0130133', 'increased size of the hyoid arch', 0.4090909090909091, 5.725717590856133, 1.5304701939081158, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(32592, 'HP:0011830', 'Abnormal oral mucosa morphology', 'XPO:0103009', 'abnormal manicotto glandulare morphology', 0.42, 5.725717590856133, 1.5507422055775666, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(32593, 'HP:0011830', 'Abnormal oral mucosa morphology', 'XPO:0130701', 'increased size of the upper jaw', 0.4230769230769231, 7.312692920701687, 1.7589291117884391, 'UPHENO:0076800', 'abnormal mouth morphology'),
(32594, 'HP:0011830', 'Abnormal oral mucosa morphology', 'XPO:0128654', 'decreased size of the hyoid arch', 0.40298507462686567, 5.725717590856133, 1.5190058362769763, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(32595, 'HP:0011830', 'Abnormal oral mucosa morphology', 'XPO:0103199', 'abnormal tongue morphology', 0.6481481481481481, 7.884497199543557, 2.260602189453823, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(32596, 'HP:0011830', 'Abnormal oral mucosa morphology', 'XPO:0141835', 'edematous head', 0.42, 4.5318002188002176, 1.3796217205799897, 'UPHENO:0087907', 'abnormal head morphology'),
(32597, 'HP:0011830', 'Abnormal oral mucosa morphology', 'XPO:0139987', 'abnormally necrotic branchial arch', 0.43548387096774194, 5.725717590856133, 1.5790686053918375, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(32598, 'HP:0011830', 'Abnormal oral mucosa morphology', 'XPO:0115558', 'abnormally incomplete structure of mouth', 0.6, 7.312692920701687, 2.094663637059901, 'UPHENO:0076800', 'abnormal mouth morphology'),
(32599, 'HP:0011830', 'Abnormal oral mucosa morphology', 'XPO:0128653', 'decreased size of the oral epithelium', 0.4788732394366197, 11.317232080316854, 2.327986165714343, 'UPHENO:0087132', 'abnormal mouth mucosa morphology'),
(32600, 'HP:0011830', 'Abnormal oral mucosa morphology', 'XPO:0103735', 'increased size of the mouth', 0.5555555555555556, 7.884497199543557, 2.0929109445861864, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(32601, 'HP:0011830', 'Abnormal oral mucosa morphology', 'XPO:0103739', 'increased size of the pharyngeal region', 0.40384615384615385, 4.5318002188002176, 1.3528303989641963, 'UPHENO:0087907', 'abnormal head morphology'),
(32602, 'HP:0011830', 'Abnormal oral mucosa morphology', 'XPO:0101328', 'abnormal oral epithelium', 0.41818181818181815, 7.0866363731414825, 1.721482641014341, 'HP:0000153', 'Abnormality of the mouth'),
(32603, 'HP:0011830', 'Abnormal oral mucosa morphology', 'XPO:0102279', 'abnormal mouth morphology', 0.6111111111111112, 7.312692920701687, 2.1139697008198497, 'UPHENO:0076800', 'abnormal mouth morphology'),
(32604, 'HP:0011830', 'Abnormal oral mucosa morphology', 'XPO:0103707', 'increased pigmentation in the head', 0.4117647058823529, 4.5318002188002176, 1.3660290568695288, 'UPHENO:0087907', 'abnormal head morphology'),
(32605, 'HP:0011830', 'Abnormal oral mucosa morphology', 'XPO:0129821', 'increased size of the pharyngeal cavity', 0.40384615384615385, 5.725717590856133, 1.520627839767678, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(32606, 'HP:0011830', 'Abnormal oral mucosa morphology', 'XPO:0141833', 'edematous alimentary system', 0.42857142857142855, 5.725717590856133, 1.5664861849086864, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(32607, 'HP:0011830', 'Abnormal oral mucosa morphology', 'XPO:0140626', 'abnormally necrotic tongue', 0.5932203389830508, 7.884497199543557, 2.16269371419629, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(32608, 'HP:0011830', 'Abnormal oral mucosa morphology', 'XPO:0100647', 'abnormal mouth', 0.45098039215686275, 7.0866363731414825, 1.7877175533714584, 'HP:0000153', 'Abnormality of the mouth'),
(32609, 'HP:0011830', 'Abnormal oral mucosa morphology', 'XPO:0128341', 'decreased size of the pharyngeal cavity', 0.40384615384615385, 5.725717590856133, 1.520627839767678, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(32610, 'HP:0011830', 'Abnormal oral mucosa morphology', 'XPO:0102653', 'abnormal dorsal foregut morphology', 0.40384615384615385, 5.725717590856133, 1.520627839767678, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(32611, 'HP:0011830', 'Abnormal oral mucosa morphology', 'XPO:0102261', 'abnormal branchial arch 2 morphology', 0.4576271186440678, 5.725717590856133, 1.6187166655326515, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(32612, 'HP:0011830', 'Abnormal oral mucosa morphology', 'XPO:0129225', 'decreased size of the upper jaw', 0.4230769230769231, 7.312692920701687, 1.7589291117884391, 'UPHENO:0076800', 'abnormal mouth morphology'),
(32613, 'HP:0011830', 'Abnormal oral mucosa morphology', 'XPO:0103357', 'decreased size of the pharyngeal arch', 0.43548387096774194, 5.725717590856133, 1.5790686053918375, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(32614, 'HP:0011830', 'Abnormal oral mucosa morphology', 'XPO:0102735', 'abnormal pharyngeal mesenchyme morphology', 0.46551724137931033, 5.725717590856133, 1.6326114840378705, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(32615, 'HP:0011830', 'Abnormal oral mucosa morphology', 'XPO:0139906', 'abnormally necrotic alimentary system', 0.40384615384615385, 5.725717590856133, 1.520627839767678, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(32616, 'HP:0011830', 'Abnormal oral mucosa morphology', 'XPO:0103738', 'increased size of the pharyngeal arch', 0.43548387096774194, 5.725717590856133, 1.5790686053918375, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(32617, 'HP:0011830', 'Abnormal oral mucosa morphology', 'XPO:0101464', 'abnormal oral cavity', 0.4423076923076923, 7.0866363731414825, 1.7704445149249843, 'HP:0000153', 'Abnormality of the mouth'),
(32618, 'HP:0011830', 'Abnormal oral mucosa morphology', 'XPO:0115393', 'abnormally decreased volume of oral cavity', 0.5737704918032787, 7.884497199543557, 2.1269442484004326, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(32619, 'HP:0011830', 'Abnormal oral mucosa morphology', 'XPO:0128989', 'decreased size of the tooth', 0.4117647058823529, 7.884497199543557, 1.8018206543383524, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(32620, 'HP:0011830', 'Abnormal oral mucosa morphology', 'XPO:0102118', 'abnormal oral evagination morphology', 0.42, 5.725717590856133, 1.5507422055775666, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(32621, 'HP:0011830', 'Abnormal oral mucosa morphology', 'XPO:0103096', 'abnormal oral cavity morphology', 0.6481481481481481, 7.884497199543557, 2.260602189453823, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(32622, 'HP:0011830', 'Abnormal oral mucosa morphology', 'XPO:0127556', 'abnormally localised oral cavity', 0.41379310344827586, 7.0866363731414825, 1.7124255481192892, 'HP:0000153', 'Abnormality of the mouth'),
(32623, 'HP:0011830', 'Abnormal oral mucosa morphology', 'XPO:0102094', 'abnormal anterior foregut morphology', 0.40384615384615385, 5.725717590856133, 1.520627839767678, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(32624, 'HP:0011830', 'Abnormal oral mucosa morphology', 'XPO:0102733', 'abnormal posterior foregut morphology', 0.40384615384615385, 5.725717590856133, 1.520627839767678, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(32625, 'HP:0011830', 'Abnormal oral mucosa morphology', 'XPO:0103714', 'increased size of the branchial arch', 0.4153846153846154, 5.725717590856133, 1.5421981063659433, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(32626, 'HP:0011830', 'Abnormal oral mucosa morphology', 'XPO:0100027', 'abnormal lower jaw', 0.42592592592592593, 7.0866363731414825, 1.7373491758799184, 'HP:0000153', 'Abnormality of the mouth'),
(32627, 'HP:0011830', 'Abnormal oral mucosa morphology', 'XPO:0101634', 'abnormal head morphology', 0.4375, 4.5318002188002176, 1.4080705222839853, 'UPHENO:0087907', 'abnormal head morphology'),
(32628, 'HP:0011830', 'Abnormal oral mucosa morphology', 'XPO:0127750', 'abnormally localised tongue', 0.5689655172413793, 7.884497199543557, 2.118019600316887, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(32629, 'HP:0011830', 'Abnormal oral mucosa morphology', 'XPO:0141009', 'abnormally necrotic oral epithelium', 0.4927536231884058, 11.317232080316854, 2.3614840909987493, 'UPHENO:0087132', 'abnormal mouth mucosa morphology'),
(32630, 'HP:0001741', 'Phimosis', 'XPO:0102270', 'abnormal polar body morphology', 0.4230769230769231, 7.005035523447265, 1.7215309684419309, 'HP:0012243', 'Abnormal reproductive system morphology'),
(32631, 'HP:0001741', 'Phimosis', 'XPO:0100765', 'abnormal male genitalia', 0.5333333333333333, 8.414388317771037, 2.118413030897867, 'HP:0010461', 'Abnormality of the male genitalia'),
(32632, 'HP:0001741', 'Phimosis', 'XPO:0101262', 'abnormal oviduct', 0.43137254901960786, 7.005035523447265, 1.7383267902561792, 'UPHENO:0020950', 'abnormal reproductive system morphology'),
(32633, 'HP:0001741', 'Phimosis', 'XPO:0100414', 'abnormal testis', 0.43636363636363634, 8.414388317771037, 1.916176683951214, 'HP:0010461', 'Abnormality of the male genitalia'),
(32634, 'HP:0001741', 'Phimosis', 'XPO:0139867', 'abnormally necrotic genital system', 0.4230769230769231, 7.005035523447265, 1.7215309684419309, 'HP:0012243', 'Abnormal reproductive system morphology'),
(32635, 'HP:0001741', 'Phimosis', 'XPO:0139866', 'abnormally necrotic male genitalia', 0.44642857142857145, 9.103525386846629, 2.015954819288784, 'UPHENO:0087846', 'abnormal male reproductive system morphology'),
(32636, 'HP:0001741', 'Phimosis', 'XPO:0129028', 'decreased size of the male genitalia', 0.43103448275862066, 9.103525386846629, 1.9808920607643943, 'UPHENO:0087846', 'abnormal male reproductive system morphology'),
(32637, 'HP:0001741', 'Phimosis', 'XPO:0129864', 'increased size of the genital system', 0.4074074074074074, 7.005035523447265, 1.689349981917436, 'UPHENO:0020950', 'abnormal reproductive system morphology'),
(32638, 'HP:0001741', 'Phimosis', 'XPO:0128384', 'decreased size of the genital system', 0.4074074074074074, 7.005035523447265, 1.689349981917436, 'HP:0012243', 'Abnormal reproductive system morphology'),
(32639, 'HP:0001741', 'Phimosis', 'XPO:0101752', 'abnormal genital system morphology', 0.46808510638297873, 7.005035523447265, 1.810787894318205, 'UPHENO:0020950', 'abnormal reproductive system morphology'),
(32640, 'HP:0001741', 'Phimosis', 'XPO:0125139', 'absent male genitalia', 0.43636363636363634, 8.414388317771037, 1.916176683951214, 'HP:0010461', 'Abnormality of the male genitalia'),
(32641, 'HP:0001741', 'Phimosis', 'XPO:0130505', 'increased size of the male genitalia', 0.43103448275862066, 9.103525386846629, 1.9808920607643943, 'UPHENO:0087846', 'abnormal male reproductive system morphology'),
(32642, 'HP:0001741', 'Phimosis', 'XPO:0126762', 'abnormally localised male genitalia', 0.4444444444444444, 8.414388317771037, 1.9338376718927501, 'HP:0010461', 'Abnormality of the male genitalia'),
(32643, 'HP:0001741', 'Phimosis', 'XPO:0102864', 'abnormal female genitalia morphology', 0.41509433962264153, 7.005035523447265, 1.705212771075354, 'HP:0012243', 'Abnormal reproductive system morphology'),
(32644, 'HP:0001741', 'Phimosis', 'XPO:0101372', 'abnormal seminiferous tubule', 0.41379310344827586, 8.414388317771037, 1.8659624475399805, 'HP:0010461', 'Abnormality of the male genitalia'),
(32645, 'HP:0001741', 'Phimosis', 'XPO:0101232', 'abnormal female genitalia', 0.46808510638297873, 7.005035523447265, 1.810787894318205, 'UPHENO:0020950', 'abnormal reproductive system morphology'),
(32646, 'HP:0001741', 'Phimosis', 'XPO:0102397', 'abnormal male genitalia morphology', 0.5, 9.103525386846629, 2.133486042472112, 'UPHENO:0087846', 'abnormal male reproductive system morphology'),
(32647, 'HP:0010368', 'Abnormality of the distal phalanx of the 3rd toe', 'XPO:0102566', 'abnormal claw primordium morphology', 0.42528735632183906, 7.639349617137506, 1.8024757426081115, 'HP:0001780', 'Abnormal toe morphology'),
(32648, 'HP:0010368', 'Abnormality of the distal phalanx of the 3rd toe', 'XPO:0101248', 'abnormal digit-joint region', 0.42424242424242425, 6.393467666143939, 1.6469305455909364, 'UPHENO:0002905', 'abnormal digit'),
(32649, 'HP:0010368', 'Abnormality of the distal phalanx of the 3rd toe', 'XPO:0101809', 'abnormal hindlimb digit morphology', 0.42045454545454547, 7.639349617137506, 1.792205141952758, 'UPHENO:0088132', 'abnormal pedal digit morphology'),
(32650, 'HP:0010368', 'Abnormality of the distal phalanx of the 3rd toe', 'XPO:0139979', 'abnormally necrotic claw primordium', 0.40217391304347827, 7.639349617137506, 1.7528112073555977, 'UPHENO:0088132', 'abnormal pedal digit morphology'),
(32651, 'HP:0010368', 'Abnormality of the distal phalanx of the 3rd toe', 'XPO:0102880', 'abnormal digit-joint region morphology', 0.410958904109589, 6.466375519622663, 1.630157844230185, 'UPHENO:0086700', 'abnormal digit morphology'),
(32652, 'HP:0010368', 'Abnormality of the distal phalanx of the 3rd toe', 'XPO:0102051', 'abnormal hindlimb digit 2 morphology', 0.4111111111111111, 7.639349617137506, 1.7721798749753483, 'UPHENO:0088132', 'abnormal pedal digit morphology'),
(32653, 'HP:0010368', 'Abnormality of the distal phalanx of the 3rd toe', 'XPO:0102948', 'abnormal hindlimb digit 5 morphology', 0.4111111111111111, 7.639349617137506, 1.7721798749753483, 'UPHENO:0088132', 'abnormal pedal digit morphology'),
(32654, 'HP:0010368', 'Abnormality of the distal phalanx of the 3rd toe', 'XPO:0101872', 'abnormal hindlimb digit 1 morphology', 0.4111111111111111, 7.639349617137506, 1.7721798749753483, 'HP:0001780', 'Abnormal toe morphology'),
(32655, 'HP:0010368', 'Abnormality of the distal phalanx of the 3rd toe', 'XPO:0103627', 'abnormally increased number of hindlimb digit', 0.41935483870967744, 7.639349617137506, 1.7898598343282457, 'UPHENO:0088132', 'abnormal pedal digit morphology'),
(32656, 'HP:0010368', 'Abnormality of the distal phalanx of the 3rd toe', 'XPO:0102876', 'abnormal hindlimb digit 4 morphology', 0.4111111111111111, 7.639349617137506, 1.7721798749753483, 'HP:0001780', 'Abnormal toe morphology'),
(32657, 'HP:0010368', 'Abnormality of the distal phalanx of the 3rd toe', 'XPO:0100178', 'abnormal digit', 0.4444444444444444, 6.393467666143939, 1.6856871551248356, 'UPHENO:0002905', 'abnormal digit'),
(32658, 'HP:0010368', 'Abnormality of the distal phalanx of the 3rd toe', 'XPO:0102180', 'abnormal hindlimb digit 3 morphology', 0.4111111111111111, 7.639349617137506, 1.7721798749753483, 'UPHENO:0088132', 'abnormal pedal digit morphology'),
(32659, 'HP:0010368', 'Abnormality of the distal phalanx of the 3rd toe', 'XPO:0101810', 'abnormal digit morphology', 0.410958904109589, 6.466375519622663, 1.630157844230185, 'UPHENO:0086700', 'abnormal digit morphology'),
(32660, 'HP:0032863', 'Typical absence status epilepticus', 'XPO:0100031', 'abnormal central nervous system', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(32661, 'HP:0032863', 'Typical absence status epilepticus', 'XPO:0100032', 'abnormal nervous system', 0.43333333333333335, 3.94131651835137, 1.3068679445984308, 'UPHENO:0004523', 'abnormal nervous system'),
(32662, 'HP:0032863', 'Typical absence status epilepticus', 'XPO:0100273', 'abnormal visual system', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(32663, 'HP:0032863', 'Typical absence status epilepticus', 'XPO:0100274', 'abnormal sensory system', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(32664, 'HP:0032863', 'Typical absence status epilepticus', 'XPO:0100587', 'abnormal vestibuloauditory system', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(32665, 'HP:0032863', 'Typical absence status epilepticus', 'XPO:0107253', 'abnormal enteric nervous system', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(32666, 'HP:0032863', 'Typical absence status epilepticus', 'XPO:0100427', 'abnormal olfactory system', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(32667, 'HP:0032863', 'Typical absence status epilepticus', 'XPO:0100642', 'abnormal gustatory system', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(32668, 'HP:0032220', 'Interface hepatitis', 'XPO:0100042', 'abnormal hepatic vein', 0.40229885057471265, 10.01729298920255, 2.0074724046487695, 'UPHENO:0019492', 'abnormal liver morphology'),
(32669, 'HP:0034614', 'Elevated circulating erythritol concentration', 'XPO:0141783', 'abnormal collagen metabolic process', 0.40625, 6.913987275905781, 1.6759496802818168, 'UPHENO:0049873', 'abnormal metabolic process'),
(32670, 'HP:0034614', 'Elevated circulating erythritol concentration', 'XPO:0141778', 'abnormal biosynthetic process', 0.40625, 6.913987275905781, 1.6759496802818168, 'UPHENO:0049873', 'abnormal metabolic process'),
(32671, 'HP:0034614', 'Elevated circulating erythritol concentration', 'XPO:0141918', 'abnormal tyrosine metabolic process', 0.4107142857142857, 7.5690956201444655, 1.763160713358474, 'UPHENO:0050116', 'abnormal primary metabolic process'),
(32672, 'HP:0034614', 'Elevated circulating erythritol concentration', 'XPO:0141792', 'abnormal small molecule metabolic process', 0.40625, 6.913987275905781, 1.6759496802818168, 'UPHENO:0049873', 'abnormal metabolic process'),
(32673, 'HP:0034614', 'Elevated circulating erythritol concentration', 'XPO:0141777', 'abnormal catabolic process', 0.40625, 6.913987275905781, 1.6759496802818168, 'UPHENO:0049873', 'abnormal metabolic process'),
(32674, 'HP:0034614', 'Elevated circulating erythritol concentration', 'XPO:0141898', 'abnormal maltose metabolic process', 0.45454545454545453, 10.954662000932146, 2.231455089981764, 'UPHENO:0050342', 'abnormal carbohydrate metabolic process'),
(32675, 'HP:0034614', 'Elevated circulating erythritol concentration', 'XPO:0141776', 'abnormal metabolic process', 0.43333333333333335, 6.913987275905781, 1.730913386883499, 'UPHENO:0049873', 'abnormal metabolic process'),
(32676, 'HP:0034614', 'Elevated circulating erythritol concentration', 'XPO:0141859', 'abnormal lactose catabolic process', 0.42857142857142855, 10.954662000932146, 2.1667614412428136, 'UPHENO:0050342', 'abnormal carbohydrate metabolic process'),
(32677, 'HP:0034614', 'Elevated circulating erythritol concentration', 'XPO:0141882', 'abnormal gamma-aminobutyric acid metabolic process', 0.42592592592592593, 7.5690956201444655, 1.7955149847416763, 'UPHENO:0050116', 'abnormal primary metabolic process'),
(32678, 'HP:0034614', 'Elevated circulating erythritol concentration', 'XPO:0141781', 'abnormal secondary metabolic process', 0.40625, 6.913987275905781, 1.6759496802818168, 'UPHENO:0049873', 'abnormal metabolic process'),
(32679, 'HP:0034614', 'Elevated circulating erythritol concentration', 'XPO:0141873', 'abnormal tricarboxylic acid metabolic process', 0.44, 7.41682187759612, 1.8064887561627094, 'HP:0430071', 'Abnormal circulating organic compound concentration'),
(32680, 'HP:0034614', 'Elevated circulating erythritol concentration', 'XPO:0141904', 'abnormal glucosamine metabolic process', 0.40625, 6.913987275905781, 1.6759496802818168, 'UPHENO:0049873', 'abnormal metabolic process'),
(32681, 'HP:0034614', 'Elevated circulating erythritol concentration', 'XPO:0141905', 'abnormal ornithine metabolic process', 0.41818181818181815, 7.5690956201444655, 1.7791172441477963, 'UPHENO:0050116', 'abnormal primary metabolic process'),
(32682, 'HP:0034614', 'Elevated circulating erythritol concentration', 'XPO:0141869', 'abnormal alpha-amino acid metabolic process', 0.4339622641509434, 7.5690956201444655, 1.812374650256641, 'UPHENO:0050116', 'abnormal primary metabolic process'),
(32683, 'HP:0034614', 'Elevated circulating erythritol concentration', 'XPO:0141881', 'abnormal fructose metabolic process', 0.42857142857142855, 10.954662000932146, 2.1667614412428136, 'UPHENO:0050342', 'abnormal carbohydrate metabolic process'),
(32684, 'HP:0034614', 'Elevated circulating erythritol concentration', 'XPO:0141843', 'abnormal alanine metabolic process', 0.41818181818181815, 7.5690956201444655, 1.7791172441477963, 'UPHENO:0050116', 'abnormal primary metabolic process'),
(32685, 'HP:0034614', 'Elevated circulating erythritol concentration', 'XPO:0141857', 'abnormal glycine metabolic process', 0.40350877192982454, 7.5690956201444655, 1.7476259549182447, 'UPHENO:0050116', 'abnormal primary metabolic process'),
(32686, 'HP:0034614', 'Elevated circulating erythritol concentration', 'XPO:0141786', 'abnormal pigment metabolic process', 0.40625, 6.913987275905781, 1.6759496802818168, 'UPHENO:0049873', 'abnormal metabolic process'),
(32687, 'HP:0034614', 'Elevated circulating erythritol concentration', 'XPO:0141858', 'abnormal serine family amino acid metabolic process', 0.41818181818181815, 7.5690956201444655, 1.7791172441477963, 'UPHENO:0050116', 'abnormal primary metabolic process'),
(32688, 'HP:0034614', 'Elevated circulating erythritol concentration', 'XPO:0141868', 'abnormal asparagine metabolic process', 0.4107142857142857, 7.5690956201444655, 1.763160713358474, 'UPHENO:0050116', 'abnormal primary metabolic process'),
(32689, 'HP:0034614', 'Elevated circulating erythritol concentration', 'XPO:0141797', 'abnormal hydrogen metabolic process', 0.40625, 6.913987275905781, 1.6759496802818168, 'UPHENO:0049873', 'abnormal metabolic process'),
(32690, 'HP:0034614', 'Elevated circulating erythritol concentration', 'XPO:0141900', 'abnormal mannose metabolic process', 0.42857142857142855, 10.954662000932146, 2.1667614412428136, 'UPHENO:0050342', 'abnormal carbohydrate metabolic process'),
(32691, 'HP:0034614', 'Elevated circulating erythritol concentration', 'XPO:0141895', 'abnormal leucine metabolic process', 0.4107142857142857, 7.5690956201444655, 1.763160713358474, 'UPHENO:0050116', 'abnormal primary metabolic process'),
(32692, 'HP:0034614', 'Elevated circulating erythritol concentration', 'XPO:0141889', 'abnormal homoserine metabolic process', 0.40350877192982454, 7.5690956201444655, 1.7476259549182447, 'UPHENO:0050116', 'abnormal primary metabolic process'),
(32693, 'HP:0034614', 'Elevated circulating erythritol concentration', 'XPO:0141887', 'abnormal histidine metabolic process', 0.4107142857142857, 7.5690956201444655, 1.763160713358474, 'UPHENO:0050116', 'abnormal primary metabolic process'),
(32694, 'HP:0034614', 'Elevated circulating erythritol concentration', 'XPO:0141847', 'abnormal arginine metabolic process', 0.4107142857142857, 7.5690956201444655, 1.763160713358474, 'UPHENO:0050116', 'abnormal primary metabolic process'),
(32695, 'HP:0034614', 'Elevated circulating erythritol concentration', 'XPO:0141917', 'abnormal tryptophan metabolic process', 0.4107142857142857, 7.5690956201444655, 1.763160713358474, 'UPHENO:0050116', 'abnormal primary metabolic process'),
(32696, 'HP:0034614', 'Elevated circulating erythritol concentration', 'XPO:0141782', 'abnormal methylation', 0.40625, 6.913987275905781, 1.6759496802818168, 'UPHENO:0049873', 'abnormal metabolic process'),
(32697, 'HP:0034614', 'Elevated circulating erythritol concentration', 'XPO:0141852', 'abnormal glucose metabolic process', 0.42857142857142855, 10.954662000932146, 2.1667614412428136, 'UPHENO:0050342', 'abnormal carbohydrate metabolic process'),
(32698, 'HP:0034614', 'Elevated circulating erythritol concentration', 'XPO:0141850', 'abnormal galactose metabolic process', 0.42857142857142855, 10.954662000932146, 2.1667614412428136, 'UPHENO:0050342', 'abnormal carbohydrate metabolic process'),
(32699, 'HP:0034614', 'Elevated circulating erythritol concentration', 'XPO:0141922', 'abnormal valine metabolic process', 0.4107142857142857, 7.5690956201444655, 1.763160713358474, 'UPHENO:0050116', 'abnormal primary metabolic process'),
(32700, 'HP:0034614', 'Elevated circulating erythritol concentration', 'XPO:0141910', 'abnormal D-ribose metabolic process', 0.42857142857142855, 10.954662000932146, 2.1667614412428136, 'UPHENO:0050342', 'abnormal carbohydrate metabolic process'),
(32701, 'HP:0034614', 'Elevated circulating erythritol concentration', 'XPO:0141798', 'abnormal lipid metabolic process', 0.42424242424242425, 7.5690956201444655, 1.7919630228363541, 'UPHENO:0050116', 'abnormal primary metabolic process'),
(32702, 'HP:0034614', 'Elevated circulating erythritol concentration', 'XPO:0141896', 'abnormal lysine metabolic process', 0.4107142857142857, 7.5690956201444655, 1.763160713358474, 'UPHENO:0050116', 'abnormal primary metabolic process'),
(32703, 'HP:0034614', 'Elevated circulating erythritol concentration', 'XPO:0141883', 'abnormal glycerol metabolic process', 0.42857142857142855, 10.954662000932146, 2.1667614412428136, 'UPHENO:0050342', 'abnormal carbohydrate metabolic process'),
(32704, 'HP:0034614', 'Elevated circulating erythritol concentration', 'XPO:0141796', 'abnormal demethylation', 0.40625, 6.913987275905781, 1.6759496802818168, 'UPHENO:0049873', 'abnormal metabolic process'),
(32705, 'HP:0034614', 'Elevated circulating erythritol concentration', 'XPO:0141787', 'abnormal hormone metabolic process', 0.40625, 6.913987275905781, 1.6759496802818168, 'UPHENO:0049873', 'abnormal metabolic process'),
(32706, 'HP:0034614', 'Elevated circulating erythritol concentration', 'XPO:0141791', 'abnormal primary metabolic process', 0.45161290322580644, 7.5690956201444655, 1.8488648538514594, 'UPHENO:0050116', 'abnormal primary metabolic process'),
(32707, 'HP:0034614', 'Elevated circulating erythritol concentration', 'XPO:0141912', 'abnormal D-serine metabolic process', 0.40350877192982454, 7.5690956201444655, 1.7476259549182447, 'UPHENO:0050116', 'abnormal primary metabolic process'),
(32708, 'HP:0034614', 'Elevated circulating erythritol concentration', 'XPO:0141893', 'abnormal isoleucine metabolic process', 0.4107142857142857, 7.5690956201444655, 1.763160713358474, 'UPHENO:0050116', 'abnormal primary metabolic process'),
(32709, 'HP:0034614', 'Elevated circulating erythritol concentration', 'XPO:0141775', 'abnormal nitrogen compound metabolic process', 0.40625, 6.913987275905781, 1.6759496802818168, 'UPHENO:0049873', 'abnormal metabolic process'),
(32710, 'HP:0034614', 'Elevated circulating erythritol concentration', 'XPO:0141913', 'abnormal L-serine metabolic process', 0.40350877192982454, 7.5690956201444655, 1.7476259549182447, 'UPHENO:0050116', 'abnormal primary metabolic process'),
(32711, 'HP:0034614', 'Elevated circulating erythritol concentration', 'XPO:0141888', 'abnormal threonine metabolic process', 0.4107142857142857, 7.5690956201444655, 1.763160713358474, 'UPHENO:0050116', 'abnormal primary metabolic process'),
(32712, 'HP:0034614', 'Elevated circulating erythritol concentration', 'XPO:0141794', 'abnormal prosthetic group metabolic process', 0.40625, 6.913987275905781, 1.6759496802818168, 'UPHENO:0049873', 'abnormal metabolic process'),
(32713, 'HP:0034614', 'Elevated circulating erythritol concentration', 'XPO:0141848', 'abnormal proline metabolic process', 0.4107142857142857, 7.5690956201444655, 1.763160713358474, 'UPHENO:0050116', 'abnormal primary metabolic process'),
(32714, 'HP:0004481', 'Progressive macrocephaly', 'XPO:0129957', 'increased size of the neurocranium', 0.5151515151515151, 7.024697770424301, 1.902310095624672, 'HP:0000929', 'Abnormal skull morphology'),
(32715, 'HP:0004481', 'Progressive macrocephaly', 'XPO:0130449', 'increased size of the fenestra subocularis', 0.47540983606557374, 5.972749669260594, 1.6850827698139603, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(32716, 'HP:0004481', 'Progressive macrocephaly', 'XPO:0102351', 'abnormal sphenoid region morphology', 0.5081967213114754, 7.024697770424301, 1.8894254087244782, 'HP:0000929', 'Abnormal skull morphology'),
(32717, 'HP:0004481', 'Progressive macrocephaly', 'XPO:0103332', 'decreased size of the chondrocranium', 0.40298507462686567, 4.6864066944795475, 1.3742459574278119, 'UPHENO:0075195', 'abnormal size of anatomical entity'),
(32718, 'HP:0004481', 'Progressive macrocephaly', 'XPO:0141829', 'increased width of head', 0.65, 13.964122330181212, 3.012752813394718, 'HP:0040194', 'Increased head circumference'),
(32719, 'HP:0004481', 'Progressive macrocephaly', 'XPO:0129688', 'increased size of the olfactory region', 0.5230769230769231, 7.024697770424301, 1.9168873976576886, 'HP:0000929', 'Abnormal skull morphology'),
(32720, 'HP:0004481', 'Progressive macrocephaly', 'XPO:0128034', 'decreased size of the cranium', 0.421875, 4.6864066944795475, 1.406085994608281, 'UPHENO:0075195', 'abnormal size of anatomical entity'),
(32721, 'HP:0004481', 'Progressive macrocephaly', 'XPO:0103138', 'abnormal upper jaw morphology', 0.4025974025974026, 7.024697770424301, 1.6817030286006471, 'HP:0000929', 'Abnormal skull morphology'),
(32722, 'HP:0004481', 'Progressive macrocephaly', 'XPO:0129718', 'increased size of the ethmoid region', 0.4603174603174603, 5.972749669260594, 1.658119705831273, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(32723, 'HP:0004481', 'Progressive macrocephaly', 'XPO:0128209', 'decreased size of the sphenoid region', 0.47761194029850745, 7.024697770424301, 1.831687618602842, 'HP:0000929', 'Abnormal skull morphology'),
(32724, 'HP:0004481', 'Progressive macrocephaly', 'XPO:0128905', 'decreased size of the occipital region', 0.48484848484848486, 7.024697770424301, 1.8455118722210249, 'HP:0000929', 'Abnormal skull morphology'),
(32725, 'HP:0004481', 'Progressive macrocephaly', 'XPO:0101681', 'abnormal chondrocranium morphology', 0.43333333333333335, 4.638757693672553, 1.4177899470389728, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(32726, 'HP:0004481', 'Progressive macrocephaly', 'XPO:0102259', 'abnormal pharyngeal region morphology', 0.4117647058823529, 4.5318002188002176, 1.3660290568695288, 'UPHENO:0087907', 'abnormal head morphology'),
(32727, 'HP:0004481', 'Progressive macrocephaly', 'XPO:0130383', 'increased size of the occipital region', 0.53125, 7.024697770424301, 1.9318050342976927, 'HP:0000929', 'Abnormal skull morphology'),
(32728, 'HP:0004481', 'Progressive macrocephaly', 'XPO:0130358', 'increased size of the lower jaw', 0.43037974683544306, 7.024697770424301, 1.7387603768290534, 'HP:0000929', 'Abnormal skull morphology'),
(32729, 'HP:0004481', 'Progressive macrocephaly', 'XPO:0130138', 'increased size of the braincase and otic capsule skeleton', 0.43283582089552236, 5.972749669260594, 1.6078619362674984, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(32730, 'HP:0004481', 'Progressive macrocephaly', 'XPO:0129689', 'increased size of the sphenoid region', 0.5230769230769231, 7.024697770424301, 1.9168873976576886, 'HP:0000929', 'Abnormal skull morphology'),
(32731, 'HP:0004481', 'Progressive macrocephaly', 'XPO:0128668', 'decreased size of the fenestra basicranialis', 0.42857142857142855, 4.6864066944795475, 1.4172014718873975, 'UPHENO:0075195', 'abnormal size of anatomical entity'),
(32732, 'HP:0004481', 'Progressive macrocephaly', 'XPO:0140926', 'abnormally necrotic neurocranium', 0.4696969696969697, 7.024697770424301, 1.8164468766813286, 'HP:0000929', 'Abnormal skull morphology'),
(32733, 'HP:0004481', 'Progressive macrocephaly', 'XPO:0130324', 'increased size of the choana', 0.4927536231884058, 7.024697770424301, 1.860495976394491, 'HP:0000929', 'Abnormal skull morphology'),
(32734, 'HP:0004481', 'Progressive macrocephaly', 'XPO:0128208', 'decreased size of the olfactory region', 0.47761194029850745, 7.024697770424301, 1.831687618602842, 'HP:0000929', 'Abnormal skull morphology'),
(32735, 'HP:0004481', 'Progressive macrocephaly', 'XPO:0128238', 'decreased size of the ethmoid region', 0.4153846153846154, 4.6864066944795475, 1.3952280252067308, 'UPHENO:0075195', 'abnormal size of anatomical entity'),
(32736, 'HP:0004481', 'Progressive macrocephaly', 'XPO:0129790', 'increased size of the mandibular arch skeleton', 0.4264705882352941, 5.972749669260594, 1.5959956343398074, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(32737, 'HP:0004481', 'Progressive macrocephaly', 'XPO:0141185', 'abnormally necrotic occipital region', 0.47692307692307695, 7.024697770424301, 1.8303662133915815, 'HP:0000929', 'Abnormal skull morphology'),
(32738, 'HP:0004481', 'Progressive macrocephaly', 'XPO:0131638', 'increased size of the intercanthal region', 0.42857142857142855, 5.972749669260594, 1.5999218287949384, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(32739, 'HP:0004481', 'Progressive macrocephaly', 'XPO:0130880', 'increased size of the suspensorium', 0.453125, 5.972749669260594, 1.6451146446019216, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(32740, 'HP:0004481', 'Progressive macrocephaly', 'XPO:0130273', 'increased size of the pharyngeal pouch', 0.4067796610169492, 5.972749669260594, 1.5587152035573786, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(32741, 'HP:0004481', 'Progressive macrocephaly', 'XPO:0130787', 'increased size of the lateral nasal prominence', 0.41379310344827586, 5.972749669260594, 1.572094978607528, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(32742, 'HP:0004481', 'Progressive macrocephaly', 'XPO:0130640', 'increased size of the medial nasal prominence', 0.41379310344827586, 5.972749669260594, 1.572094978607528, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(32743, 'HP:0004481', 'Progressive macrocephaly', 'XPO:0130062', 'increased size of the head region', 0.42857142857142855, 5.972749669260594, 1.5999218287949384, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(32744, 'HP:0004481', 'Progressive macrocephaly', 'XPO:0103176', 'abnormal fenestra basicranialis morphology', 0.4406779661016949, 4.638757693672553, 1.4297546312868548, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(32745, 'HP:0004481', 'Progressive macrocephaly', 'XPO:0102776', 'abnormal fenestra subocularis morphology', 0.4406779661016949, 4.638757693672553, 1.4297546312868548, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(32746, 'HP:0004481', 'Progressive macrocephaly', 'XPO:0129514', 'increased size of the cranium', 0.46774193548387094, 5.972749669260594, 1.6714381503545384, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(32747, 'HP:0004481', 'Progressive macrocephaly', 'XPO:0103739', 'increased size of the pharyngeal region', 0.4528301886792453, 5.972749669260594, 1.6445793868540293, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(32748, 'HP:0004481', 'Progressive macrocephaly', 'XPO:0129771', 'increased size of the dermatocranium', 0.4461538461538462, 5.972749669260594, 1.6324108664961547, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(32749, 'HP:0004481', 'Progressive macrocephaly', 'XPO:0130060', 'increased size of the postcranial axial skeleton', 0.4126984126984127, 6.272837960958401, 1.6089718050984856, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(32750, 'HP:0004481', 'Progressive macrocephaly', 'XPO:0141201', 'abnormally necrotic sphenoid region', 0.4696969696969697, 7.024697770424301, 1.8164468766813286, 'HP:0000929', 'Abnormal skull morphology'),
(32751, 'HP:0004481', 'Progressive macrocephaly', 'XPO:0130701', 'increased size of the upper jaw', 0.41975308641975306, 7.024697770424301, 1.717160030486838, 'HP:0000929', 'Abnormal skull morphology'),
(32752, 'HP:0004481', 'Progressive macrocephaly', 'XPO:0102720', 'abnormal dermatocranium morphology', 0.43333333333333335, 4.638757693672553, 1.4177899470389728, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(32753, 'HP:0004481', 'Progressive macrocephaly', 'XPO:0101634', 'abnormal head morphology', 0.40384615384615385, 4.5318002188002176, 1.3528303989641963, 'UPHENO:0087907', 'abnormal head morphology'),
(32754, 'HP:0004481', 'Progressive macrocephaly', 'XPO:0128033', 'decreased size of the splanchnocranium', 0.40298507462686567, 4.6864066944795475, 1.3742459574278119, 'UPHENO:0075195', 'abnormal size of anatomical entity'),
(32755, 'HP:0004481', 'Progressive macrocephaly', 'XPO:0142045', 'increased size of the nasal region', 0.4067796610169492, 5.972749669260594, 1.5587152035573786, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(32756, 'HP:0004481', 'Progressive macrocephaly', 'XPO:0102052', 'abnormal choana morphology', 0.4696969696969697, 7.024697770424301, 1.8164468766813286, 'HP:0000929', 'Abnormal skull morphology'),
(32757, 'HP:0004481', 'Progressive macrocephaly', 'XPO:0103152', 'abnormal otic region morphology', 0.5081967213114754, 7.024697770424301, 1.8894254087244782, 'HP:0000929', 'Abnormal skull morphology'),
(32758, 'HP:0004481', 'Progressive macrocephaly', 'XPO:0102665', 'abnormal suspensorium morphology', 0.43333333333333335, 4.638757693672553, 1.4177899470389728, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(32759, 'HP:0004481', 'Progressive macrocephaly', 'XPO:0140132', 'abnormally necrotic ethmoid region', 0.40625, 4.638757693672553, 1.3727692133255593, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(32760, 'HP:0004481', 'Progressive macrocephaly', 'XPO:0140644', 'abnormally necrotic otic region', 0.4696969696969697, 7.024697770424301, 1.8164468766813286, 'HP:0000929', 'Abnormal skull morphology'),
(32761, 'HP:0004481', 'Progressive macrocephaly', 'XPO:0102092', 'abnormal ethmoid region morphology', 0.4406779661016949, 4.638757693672553, 1.4297546312868548, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(32762, 'HP:0004481', 'Progressive macrocephaly', 'XPO:0103381', 'increased size of the head', 0.6964285714285714, 13.964122330181212, 3.1184954330032157, 'HP:0040194', 'Increased head circumference'),
(32763, 'HP:0004481', 'Progressive macrocephaly', 'XPO:0140560', 'abnormally necrotic orbital region', 0.4246575342465753, 7.024697770424301, 1.727162654186281, 'HP:0000929', 'Abnormal skull morphology'),
(32764, 'HP:0004481', 'Progressive macrocephaly', 'XPO:0129513', 'increased size of the splanchnocranium', 0.4461538461538462, 5.972749669260594, 1.6324108664961547, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(32765, 'HP:0004481', 'Progressive macrocephaly', 'XPO:0140672', 'abnormally necrotic olfactory region', 0.4696969696969697, 7.024697770424301, 1.8164468766813286, 'HP:0000929', 'Abnormal skull morphology'),
(32766, 'HP:0004481', 'Progressive macrocephaly', 'XPO:0102005', 'abnormal splanchnocranium morphology', 0.43333333333333335, 4.638757693672553, 1.4177899470389728, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(32767, 'HP:0004481', 'Progressive macrocephaly', 'XPO:0102921', 'abnormal orbital region morphology', 0.45588235294117646, 7.024697770424301, 1.78953506483714, 'HP:0000929', 'Abnormal skull morphology'),
(32768, 'HP:0004481', 'Progressive macrocephaly', 'XPO:0129786', 'increased size of the articular system', 0.40350877192982454, 5.972749669260594, 1.5524357906488784, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(32769, 'HP:0004481', 'Progressive macrocephaly', 'XPO:0128971', 'decreased size of the fenestra subocularis', 0.42857142857142855, 4.6864066944795475, 1.4172014718873975, 'UPHENO:0075195', 'abnormal size of anatomical entity'),
(32770, 'HP:0004481', 'Progressive macrocephaly', 'XPO:0128846', 'decreased size of the choana', 0.4507042253521127, 7.024697770424301, 1.7793428469386663, 'HP:0000929', 'Abnormal skull morphology'),
(32771, 'HP:0004481', 'Progressive macrocephaly', 'XPO:0101997', 'abnormal braincase and otic capsule skeleton morphology', 0.41935483870967744, 4.638757693672553, 1.394734915474381, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(32772, 'HP:0004481', 'Progressive macrocephaly', 'XPO:0129291', 'decreased size of the orbital region', 0.42105263157894735, 7.024697770424301, 1.7198161187417438, 'HP:0000929', 'Abnormal skull morphology'),
(32773, 'HP:0004481', 'Progressive macrocephaly', 'XPO:0139784', 'abnormally necrotic cranium', 0.4126984126984127, 4.638757693672553, 1.3836213127410304, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(32774, 'HP:0004481', 'Progressive macrocephaly', 'XPO:0130425', 'increased size of the otic region', 0.5230769230769231, 7.024697770424301, 1.9168873976576886, 'HP:0000929', 'Abnormal skull morphology'),
(32775, 'HP:0004481', 'Progressive macrocephaly', 'XPO:0130767', 'increased size of the orbital region', 0.4594594594594595, 7.024697770424301, 1.7965421900042369, 'HP:0000929', 'Abnormal skull morphology'),
(32776, 'HP:0004481', 'Progressive macrocephaly', 'XPO:0129406', 'decreased size of the suspensorium', 0.4090909090909091, 4.6864066944795475, 1.3846177721719306, 'UPHENO:0075195', 'abnormal size of anatomical entity'),
(32777, 'HP:0004481', 'Progressive macrocephaly', 'XPO:0130368', 'increased size of the elastica externa', 0.4107142857142857, 5.972749669260594, 1.5662354912849477, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(32778, 'HP:0004481', 'Progressive macrocephaly', 'XPO:0103721', 'increased size of the chondrocranium', 0.4461538461538462, 5.972749669260594, 1.6324108664961547, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(32779, 'HP:0004481', 'Progressive macrocephaly', 'XPO:0129832', 'increased size of the skeletal system', 0.4107142857142857, 5.972749669260594, 1.5662354912849477, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(32780, 'HP:0004481', 'Progressive macrocephaly', 'XPO:0130147', 'increased size of the fenestra basicranialis', 0.47540983606557374, 5.972749669260594, 1.6850827698139603, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(32781, 'HP:0004481', 'Progressive macrocephaly', 'XPO:0102215', 'abnormal mandibular arch skeleton morphology', 0.4126984126984127, 4.638757693672553, 1.3836213127410304, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(32782, 'HP:0004481', 'Progressive macrocephaly', 'XPO:0101764', 'abnormal cranium morphology', 0.4482758620689655, 4.638757693672553, 1.4420274283314136, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(32783, 'HP:0004481', 'Progressive macrocephaly', 'XPO:0102401', 'abnormal neurocranium morphology', 0.5081967213114754, 7.024697770424301, 1.8894254087244782, 'HP:0000929', 'Abnormal skull morphology'),
(32784, 'HP:0004481', 'Progressive macrocephaly', 'XPO:0128291', 'decreased size of the dermatocranium', 0.40298507462686567, 4.6864066944795475, 1.3742459574278119, 'UPHENO:0075195', 'abnormal size of anatomical entity'),
(32785, 'HP:0004481', 'Progressive macrocephaly', 'XPO:0102828', 'abnormal occipital region morphology', 0.5166666666666667, 7.024697770424301, 1.9051055564944135, 'HP:0000929', 'Abnormal skull morphology'),
(32786, 'HP:0004481', 'Progressive macrocephaly', 'XPO:0100584', 'abnormal vertebral column', 0.4107142857142857, 6.272837960958401, 1.6050994245019483, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(32787, 'HP:0004481', 'Progressive macrocephaly', 'XPO:0128477', 'decreased size of the neurocranium', 0.47058823529411764, 7.024697770424301, 1.8181694440448872, 'HP:0000929', 'Abnormal skull morphology'),
(32788, 'HP:0004481', 'Progressive macrocephaly', 'XPO:0130703', 'increased size of the circumpharyngeal ridge', 0.4067796610169492, 5.972749669260594, 1.5587152035573786, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(32789, 'HP:0004481', 'Progressive macrocephaly', 'XPO:0130319', 'increased size of the craniofacial region', 0.4067796610169492, 5.972749669260594, 1.5587152035573786, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(32790, 'HP:0004481', 'Progressive macrocephaly', 'XPO:0128947', 'decreased size of the otic region', 0.47761194029850745, 7.024697770424301, 1.831687618602842, 'HP:0000929', 'Abnormal skull morphology'),
(32791, 'HP:0004481', 'Progressive macrocephaly', 'XPO:0102564', 'abnormal olfactory region morphology', 0.5081967213114754, 7.024697770424301, 1.8894254087244782, 'HP:0000929', 'Abnormal skull morphology'),
(32792, 'HP:0004481', 'Progressive macrocephaly', 'XPO:0101659', 'abnormal lower jaw morphology', 0.41333333333333333, 7.024697770424301, 1.7039782114536297, 'HP:0000929', 'Abnormal skull morphology'),
(32793, 'HP:0011342', 'Mild global developmental delay', 'XPO:0100274', 'abnormal sensory system', 0.4482758620689655, 3.94131651835137, 1.3292091859262085, 'UPHENO:0004523', 'abnormal nervous system'),
(32794, 'HP:0011342', 'Mild global developmental delay', 'XPO:0100642', 'abnormal gustatory system', 0.43333333333333335, 3.94131651835137, 1.3068679445984308, 'UPHENO:0004523', 'abnormal nervous system'),
(32795, 'HP:0011342', 'Mild global developmental delay', 'XPO:0100196', 'abnormal neuron', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(32796, 'HP:0011342', 'Mild global developmental delay', 'XPO:0100427', 'abnormal olfactory system', 0.43333333333333335, 3.94131651835137, 1.3068679445984308, 'UPHENO:0004523', 'abnormal nervous system'),
(32797, 'HP:0011342', 'Mild global developmental delay', 'XPO:0100175', 'abnormal migrating neuroblast', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(32798, 'HP:0011342', 'Mild global developmental delay', 'XPO:0100032', 'abnormal nervous system', 0.4642857142857143, 3.94131651835137, 1.3527368387638634, 'UPHENO:0004523', 'abnormal nervous system'),
(32799, 'HP:0011342', 'Mild global developmental delay', 'XPO:0100537', 'abnormal medium cavity', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(32800, 'HP:0011342', 'Mild global developmental delay', 'XPO:0100916', 'abnormal principal cavity', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(32801, 'HP:0011342', 'Mild global developmental delay', 'XPO:0100587', 'abnormal vestibuloauditory system', 0.43333333333333335, 3.94131651835137, 1.3068679445984308, 'UPHENO:0004523', 'abnormal nervous system'),
(32802, 'HP:0011342', 'Mild global developmental delay', 'XPO:0100273', 'abnormal visual system', 0.43333333333333335, 3.94131651835137, 1.3068679445984308, 'UPHENO:0004523', 'abnormal nervous system'),
(32803, 'HP:0011342', 'Mild global developmental delay', 'XPO:0101501', 'abnormal parabrachial area', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(32804, 'HP:0011342', 'Mild global developmental delay', 'XPO:0100031', 'abnormal central nervous system', 0.4482758620689655, 3.94131651835137, 1.3292091859262085, 'UPHENO:0004523', 'abnormal nervous system'),
(32805, 'HP:0011342', 'Mild global developmental delay', 'XPO:0100702', 'abnormal glial cell', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(32806, 'HP:0011342', 'Mild global developmental delay', 'XPO:0142051', 'abnormal cerebrospinal fluid', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(32807, 'HP:0011342', 'Mild global developmental delay', 'XPO:0100858', 'abnormal presumptive midbrain-hindbrain boundary', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(32808, 'HP:0011342', 'Mild global developmental delay', 'XPO:0100158', 'abnormal neuromere', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(32809, 'HP:0011342', 'Mild global developmental delay', 'XPO:0100164', 'abnormal neural nucleus', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(32810, 'HP:0011342', 'Mild global developmental delay', 'XPO:0100114', 'abnormal peripheral nervous system', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(32811, 'HP:0011342', 'Mild global developmental delay', 'XPO:0107253', 'abnormal enteric nervous system', 0.4482758620689655, 3.94131651835137, 1.3292091859262085, 'UPHENO:0004523', 'abnormal nervous system'),
(32812, 'HP:0100826', 'Neoplasm of the nail', 'XPO:0128213', 'decreased size of the digit', 0.4246575342465753, 6.393467666143939, 1.6477360876031975, 'HP:0011297', 'Abnormal digit morphology'),
(32813, 'HP:0100826', 'Neoplasm of the nail', 'XPO:0115798', 'duplicated claw of hindlimb digit 2', 0.4819277108433735, 10.47734022339896, 2.2470693335075045, 'UPHENO:0003071', 'abnormal nail'),
(32814, 'HP:0100826', 'Neoplasm of the nail', 'XPO:0103617', 'abnormal number of hindlimb digit 4', 0.4027777777777778, 6.393467666143939, 1.6047263626124957, 'UPHENO:0002905', 'abnormal digit'),
(32815, 'HP:0100826', 'Neoplasm of the nail', 'XPO:0101165', 'abnormal claw of hindlimb digit 3', 0.5555555555555556, 10.47734022339896, 2.412621928225593, 'UPHENO:0003071', 'abnormal nail'),
(32816, 'HP:0100826', 'Neoplasm of the nail', 'XPO:0139922', 'abnormally necrotic claw', 0.40816326530612246, 10.47734022339896, 2.0679616527647937, 'UPHENO:0003071', 'abnormal nail'),
(32817, 'HP:0100826', 'Neoplasm of the nail', 'XPO:0124986', 'absent digit', 0.4264705882352941, 6.393467666143939, 1.6512498043735655, 'UPHENO:0002905', 'abnormal digit'),
(32818, 'HP:0100826', 'Neoplasm of the nail', 'XPO:0100177', 'abnormal hindlimb digit', 0.417910447761194, 6.393467666143939, 1.634593813491575, 'HP:0011297', 'Abnormal digit morphology'),
(32819, 'HP:0100826', 'Neoplasm of the nail', 'XPO:0100934', 'abnormal claw primordium', 0.4057971014492754, 6.393467666143939, 1.6107298492083872, 'HP:0011297', 'Abnormal digit morphology'),
(32820, 'HP:0100826', 'Neoplasm of the nail', 'XPO:0101295', 'abnormal claw of hindlimb digit 1', 0.5555555555555556, 10.47734022339896, 2.412621928225593, 'UPHENO:0003071', 'abnormal nail'),
(32821, 'HP:0100826', 'Neoplasm of the nail', 'XPO:0127409', 'abnormally localised claw of hindlimb digit 4', 0.49382716049382713, 10.47734022339896, 2.274641767850241, 'UPHENO:0003071', 'abnormal nail'),
(32822, 'HP:0100826', 'Neoplasm of the nail', 'XPO:0141558', 'abnormal claw morphology in the regenerating hindlimb', 0.40404040404040403, 10.47734022339896, 2.057490893571802, 'UPHENO:0003071', 'abnormal nail'),
(32823, 'HP:0100826', 'Neoplasm of the nail', 'XPO:0126561', 'abnormally localised claw', 0.5128205128205128, 10.47734022339896, 2.3179721711786017, 'UPHENO:0003071', 'abnormal nail'),
(32824, 'HP:0100826', 'Neoplasm of the nail', 'XPO:0102797', 'abnormal claw of hindlimb digit 3 morphology', 0.4166666666666667, 10.47734022339896, 2.08939187957076, 'UPHENO:0003071', 'abnormal nail'),
(32825, 'HP:0100826', 'Neoplasm of the nail', 'XPO:0102927', 'abnormal claw of hindlimb digit 1 morphology', 0.4166666666666667, 10.47734022339896, 2.08939187957076, 'UPHENO:0003071', 'abnormal nail'),
(32826, 'HP:0100826', 'Neoplasm of the nail', 'XPO:0103614', 'abnormal number of hindlimb digit 1', 0.4027777777777778, 6.393467666143939, 1.6047263626124957, 'UPHENO:0002905', 'abnormal digit'),
(32827, 'HP:0100826', 'Neoplasm of the nail', 'XPO:0103833', 'abnormally decreased number of digit-joint region in the regenerating forelimb', 0.4084507042253521, 6.393467666143939, 1.6159877384059913, 'UPHENO:0002905', 'abnormal digit'),
(32828, 'HP:0100826', 'Neoplasm of the nail', 'XPO:0103410', 'abnormally increased number of claw of hindlimb digit 3 in the regenerating hindlimb', 0.46511627906976744, 10.47734022339896, 2.207528368844969, 'UPHENO:0003071', 'abnormal nail'),
(32829, 'HP:0100826', 'Neoplasm of the nail', 'XPO:0127709', 'abnormally localised claw of hindlimb digit 5', 0.49382716049382713, 10.47734022339896, 2.274641767850241, 'UPHENO:0003071', 'abnormal nail'),
(32830, 'HP:0100826', 'Neoplasm of the nail', 'XPO:0129977', 'increased size of the digit-joint region', 0.44285714285714284, 6.393467666143939, 1.6826743070416301, 'HP:0011297', 'Abnormal digit morphology'),
(32831, 'HP:0100826', 'Neoplasm of the nail', 'XPO:0103044', 'abnormal claw of hindlimb digit 4 morphology', 0.4166666666666667, 10.47734022339896, 2.08939187957076, 'UPHENO:0003071', 'abnormal nail'),
(32832, 'HP:0100826', 'Neoplasm of the nail', 'XPO:0115801', 'duplicated claw of hindlimb digit 5', 0.4819277108433735, 10.47734022339896, 2.2470693335075045, 'UPHENO:0003071', 'abnormal nail'),
(32833, 'HP:0100826', 'Neoplasm of the nail', 'XPO:0103191', 'abnormal claw of hindlimb digit 5 morphology', 0.4166666666666667, 10.47734022339896, 2.08939187957076, 'UPHENO:0003071', 'abnormal nail'),
(32834, 'HP:0100826', 'Neoplasm of the nail', 'XPO:0101316', 'abnormal hindlimb digit 5', 0.4117647058823529, 6.393467666143939, 1.622530225640833, 'UPHENO:0002905', 'abnormal digit'),
(32835, 'HP:0100826', 'Neoplasm of the nail', 'XPO:0128497', 'decreased size of the digit-joint region', 0.44285714285714284, 6.393467666143939, 1.6826743070416301, 'HP:0011297', 'Abnormal digit morphology'),
(32836, 'HP:0100826', 'Neoplasm of the nail', 'XPO:0141208', 'abnormally necrotic digit-joint region', 0.45588235294117646, 6.393467666143939, 1.7072401949037608, 'UPHENO:0002905', 'abnormal digit'),
(32837, 'HP:0100826', 'Neoplasm of the nail', 'XPO:0126603', 'abnormally localised digit', 0.4393939393939394, 6.393467666143939, 1.6760820219233785, 'UPHENO:0002905', 'abnormal digit'),
(32838, 'HP:0100826', 'Neoplasm of the nail', 'XPO:0115773', 'duplicated bone element in claw of hindlimb digit 3', 0.449438202247191, 10.47734022339896, 2.1700039065256567, 'UPHENO:0003071', 'abnormal nail'),
(32839, 'HP:0100826', 'Neoplasm of the nail', 'XPO:0103618', 'abnormal number of hindlimb digit 5', 0.4027777777777778, 6.393467666143939, 1.6047263626124957, 'UPHENO:0002905', 'abnormal digit'),
(32840, 'HP:0100826', 'Neoplasm of the nail', 'XPO:0141568', 'abnormal digit-joint region morphology in the regenerating forelimb', 0.44285714285714284, 6.393467666143939, 1.6826743070416301, 'HP:0011297', 'Abnormal digit morphology'),
(32841, 'HP:0100826', 'Neoplasm of the nail', 'XPO:0115799', 'duplicated claw of hindlimb digit 3', 0.4819277108433735, 10.47734022339896, 2.2470693335075045, 'UPHENO:0003071', 'abnormal nail'),
(32842, 'HP:0100826', 'Neoplasm of the nail', 'XPO:0103409', 'abnormally increased number of claw of hindlimb digit 2 in the regenerating hindlimb', 0.46511627906976744, 10.47734022339896, 2.207528368844969, 'UPHENO:0003071', 'abnormal nail'),
(32843, 'HP:0100826', 'Neoplasm of the nail', 'XPO:0103839', 'abnormally decreased number of digit-joint region in the regenerating hindlimb', 0.4084507042253521, 6.393467666143939, 1.6159877384059913, 'HP:0011297', 'Abnormal digit morphology'),
(32844, 'HP:0100826', 'Neoplasm of the nail', 'XPO:0127382', 'abnormally localised claw of hindlimb digit 2', 0.49382716049382713, 10.47734022339896, 2.274641767850241, 'UPHENO:0003071', 'abnormal nail'),
(32845, 'HP:0100826', 'Neoplasm of the nail', 'XPO:0101810', 'abnormal digit morphology', 0.484375, 6.393467666143939, 1.759782912972072, 'UPHENO:0002905', 'abnormal digit'),
(32846, 'HP:0100826', 'Neoplasm of the nail', 'XPO:0103615', 'abnormal number of hindlimb digit 2', 0.4027777777777778, 6.393467666143939, 1.6047263626124957, 'HP:0011297', 'Abnormal digit morphology'),
(32847, 'HP:0100826', 'Neoplasm of the nail', 'XPO:0100419', 'abnormal hindlimb digit 2', 0.4117647058823529, 6.393467666143939, 1.622530225640833, 'HP:0011297', 'Abnormal digit morphology'),
(32848, 'HP:0100826', 'Neoplasm of the nail', 'XPO:0125443', 'absent digit-joint region', 0.43283582089552236, 6.393467666143939, 1.6635269236307513, 'UPHENO:0002905', 'abnormal digit'),
(32849, 'HP:0100826', 'Neoplasm of the nail', 'XPO:0115800', 'duplicated claw of hindlimb digit 4', 0.4819277108433735, 10.47734022339896, 2.2470693335075045, 'UPHENO:0003071', 'abnormal nail'),
(32850, 'HP:0100826', 'Neoplasm of the nail', 'XPO:0101248', 'abnormal digit-joint region', 0.4827586206896552, 6.393467666143939, 1.7568442252890712, 'HP:0011297', 'Abnormal digit morphology'),
(32851, 'HP:0100826', 'Neoplasm of the nail', 'XPO:0100548', 'abnormal hindlimb digit 3', 0.4117647058823529, 6.393467666143939, 1.622530225640833, 'HP:0011297', 'Abnormal digit morphology'),
(32852, 'HP:0100826', 'Neoplasm of the nail', 'XPO:0101412', 'abnormal claw of hindlimb digit 4', 0.5555555555555556, 10.47734022339896, 2.412621928225593, 'UPHENO:0003071', 'abnormal nail'),
(32853, 'HP:0100826', 'Neoplasm of the nail', 'XPO:0115772', 'duplicated bone element in claw of hindlimb digit 2', 0.449438202247191, 10.47734022339896, 2.1700039065256567, 'UPHENO:0003071', 'abnormal nail'),
(32854, 'HP:0100826', 'Neoplasm of the nail', 'XPO:0101559', 'abnormal claw of hindlimb digit 5', 0.5555555555555556, 10.47734022339896, 2.412621928225593, 'UPHENO:0003071', 'abnormal nail'),
(32855, 'HP:0100826', 'Neoplasm of the nail', 'XPO:0115797', 'duplicated claw of hindlimb digit 1', 0.4819277108433735, 10.47734022339896, 2.2470693335075045, 'UPHENO:0003071', 'abnormal nail'),
(32856, 'HP:0100826', 'Neoplasm of the nail', 'XPO:0103888', 'abnormally decreased number of claw', 0.49382716049382713, 10.47734022339896, 2.274641767850241, 'UPHENO:0003071', 'abnormal nail'),
(32857, 'HP:0100826', 'Neoplasm of the nail', 'XPO:0100237', 'abnormal claw', 0.5714285714285714, 10.47734022339896, 2.446845225229413, 'UPHENO:0003071', 'abnormal nail'),
(32858, 'HP:0100826', 'Neoplasm of the nail', 'XPO:0101244', 'abnormal hindlimb digit 4', 0.4117647058823529, 6.393467666143939, 1.622530225640833, 'UPHENO:0002905', 'abnormal digit'),
(32859, 'HP:0100826', 'Neoplasm of the nail', 'XPO:0127822', 'abnormally localised claw of hindlimb digit 3', 0.49382716049382713, 10.47734022339896, 2.274641767850241, 'UPHENO:0003071', 'abnormal nail'),
(32860, 'HP:0100826', 'Neoplasm of the nail', 'XPO:0103632', 'abnormally increased number of digit', 0.4393939393939394, 6.393467666143939, 1.6760820219233785, 'UPHENO:0002905', 'abnormal digit'),
(32861, 'HP:0100826', 'Neoplasm of the nail', 'XPO:0102457', 'abnormal claw of hindlimb digit 2 morphology', 0.4166666666666667, 10.47734022339896, 2.08939187957076, 'UPHENO:0003071', 'abnormal nail'),
(32862, 'HP:0100826', 'Neoplasm of the nail', 'XPO:0100178', 'abnormal digit', 0.509090909090909, 6.393467666143939, 1.8041220209288924, 'UPHENO:0002905', 'abnormal digit'),
(32863, 'HP:0100826', 'Neoplasm of the nail', 'XPO:0115774', 'duplicated bone element in claw of hindlimb digit 4', 0.449438202247191, 10.47734022339896, 2.1700039065256567, 'UPHENO:0003071', 'abnormal nail'),
(32864, 'HP:0100826', 'Neoplasm of the nail', 'XPO:0103408', 'abnormally increased number of claw of hindlimb digit 1 in the regenerating hindlimb', 0.46511627906976744, 10.47734022339896, 2.207528368844969, 'UPHENO:0003071', 'abnormal nail'),
(32865, 'HP:0100826', 'Neoplasm of the nail', 'XPO:0115775', 'duplicated bone element in claw of hindlimb digit 5', 0.449438202247191, 10.47734022339896, 2.1700039065256567, 'UPHENO:0003071', 'abnormal nail'),
(32866, 'HP:0100826', 'Neoplasm of the nail', 'XPO:0103411', 'abnormally increased number of claw of hindlimb digit 4 in the regenerating hindlimb', 0.46511627906976744, 10.47734022339896, 2.207528368844969, 'UPHENO:0003071', 'abnormal nail'),
(32867, 'HP:0100826', 'Neoplasm of the nail', 'XPO:0127078', 'abnormally localised digit-joint region', 0.4461538461538462, 6.393467666143939, 1.6889257501472268, 'UPHENO:0002905', 'abnormal digit'),
(32868, 'HP:0100826', 'Neoplasm of the nail', 'XPO:0103613', 'abnormal number of hindlimb digits', 0.4142857142857143, 6.393467666143939, 1.6274895756443606, 'UPHENO:0002905', 'abnormal digit'),
(32869, 'HP:0100826', 'Neoplasm of the nail', 'XPO:0103412', 'abnormally increased number of claw of hindlimb digit 5 in the regenerating hindlimb', 0.46511627906976744, 10.47734022339896, 2.207528368844969, 'UPHENO:0003071', 'abnormal nail'),
(32870, 'HP:0100826', 'Neoplasm of the nail', 'XPO:0102880', 'abnormal digit-joint region morphology', 0.484375, 6.393467666143939, 1.759782912972072, 'HP:0011297', 'Abnormal digit morphology'),
(32871, 'HP:0100826', 'Neoplasm of the nail', 'XPO:0101869', 'abnormal claw morphology', 0.43010752688172044, 10.47734022339896, 2.122824272469226, 'UPHENO:0003071', 'abnormal nail'),
(32872, 'HP:0100826', 'Neoplasm of the nail', 'XPO:0127908', 'abnormally localised claw of hindlimb digit 1', 0.49382716049382713, 10.47734022339896, 2.274641767850241, 'UPHENO:0003071', 'abnormal nail'),
(32873, 'HP:0100826', 'Neoplasm of the nail', 'XPO:0141535', 'abnormally decreased number of claw in the regenerating hindlimb', 0.45977011494252873, 10.47734022339896, 2.19480475642006, 'UPHENO:0003071', 'abnormal nail'),
(32874, 'HP:0100826', 'Neoplasm of the nail', 'XPO:0115771', 'duplicated bone element in claw of hindlimb digit 1', 0.449438202247191, 10.47734022339896, 2.1700039065256567, 'UPHENO:0003071', 'abnormal nail'),
(32875, 'HP:0100826', 'Neoplasm of the nail', 'XPO:0100825', 'abnormal claw of hindlimb digit 2', 0.5555555555555556, 10.47734022339896, 2.412621928225593, 'UPHENO:0003071', 'abnormal nail'),
(32876, 'HP:0100826', 'Neoplasm of the nail', 'XPO:0141569', 'abnormal digit-joint region morphology in the regenerating hindlimb', 0.44285714285714284, 6.393467666143939, 1.6826743070416301, 'HP:0011297', 'Abnormal digit morphology'),
(32877, 'HP:0100826', 'Neoplasm of the nail', 'XPO:0103616', 'abnormal number of hindlimb digit 3', 0.4027777777777778, 6.393467666143939, 1.6047263626124957, 'HP:0011297', 'Abnormal digit morphology'),
(32878, 'HP:0100826', 'Neoplasm of the nail', 'XPO:0100240', 'abnormal hindlimb digit 1', 0.4117647058823529, 6.393467666143939, 1.622530225640833, 'UPHENO:0002905', 'abnormal digit'),
(32879, 'HP:0100826', 'Neoplasm of the nail', 'XPO:0139962', 'abnormally necrotic digit', 0.43661971830985913, 6.393467666143939, 1.6707824668145639, 'HP:0011297', 'Abnormal digit morphology'),
(32880, 'HP:0100826', 'Neoplasm of the nail', 'XPO:0129693', 'increased size of the digit', 0.4246575342465753, 6.393467666143939, 1.6477360876031975, 'HP:0011297', 'Abnormal digit morphology'),
(32881, 'HP:0000589', 'Coloboma', 'XPO:0125990', 'absent hyaloid vein', 0.43661971830985913, 6.887869297006056, 1.734179792355427, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(32882, 'HP:0000589', 'Coloboma', 'XPO:0130285', 'increased size of the lens transitional zone', 0.40789473684210525, 6.887869297006056, 1.6761639640277146, 'HP:0012372', 'Abnormal eye morphology'),
(32883, 'HP:0000589', 'Coloboma', 'XPO:0102226', 'abnormal Jacobsons organ morphology', 0.41379310344827586, 5.788671267106304, 1.5476796336638217, 'UPHENO:0087472', 'abnormal face morphology'),
(32884, 'HP:0000589', 'Coloboma', 'XPO:0103210', 'abnormal pupil morphology', 0.4246575342465753, 6.887869297006056, 1.7102589253909142, 'HP:0012372', 'Abnormal eye morphology'),
(32885, 'HP:0000589', 'Coloboma', 'XPO:0101817', 'abnormal eye morphology', 0.49206349206349204, 6.887869297006056, 1.8409967461029664, 'HP:0012372', 'Abnormal eye morphology'),
(32886, 'HP:0000589', 'Coloboma', 'XPO:0140531', 'abnormally necrotic retinal progenitor cell region', 0.4025974025974026, 6.887869297006056, 1.6652442128423794, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(32887, 'HP:0000589', 'Coloboma', 'XPO:0102196', 'abnormal central retina morphology', 0.44285714285714284, 6.887869297006056, 1.7465228647932265, 'HP:0012372', 'Abnormal eye morphology'),
(32888, 'HP:0000589', 'Coloboma', 'XPO:0103358', 'decreased size of the pharyngeal region', 0.42857142857142855, 4.5318002188002176, 1.3936283915633758, 'UPHENO:0087907', 'abnormal head morphology'),
(32889, 'HP:0000589', 'Coloboma', 'XPO:0130062', 'increased size of the head region', 0.40384615384615385, 4.5318002188002176, 1.3528303989641963, 'UPHENO:0087907', 'abnormal head morphology'),
(32890, 'HP:0000589', 'Coloboma', 'XPO:0102862', 'abnormal iris morphology', 0.4246575342465753, 6.887869297006056, 1.7102589253909142, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(32891, 'HP:0000589', 'Coloboma', 'XPO:0140487', 'abnormally necrotic retinal layer', 0.4189189189189189, 6.887869297006056, 1.6986638159319787, 'HP:0012372', 'Abnormal eye morphology'),
(32892, 'HP:0000589', 'Coloboma', 'XPO:0130413', 'increased size of the central retina', 0.41333333333333333, 6.887869297006056, 1.6873013886368484, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(32893, 'HP:0000589', 'Coloboma', 'XPO:0141337', 'increased pigmentation in the eye', 0.4696969696969697, 6.887869297006056, 1.7986693238259617, 'HP:0012372', 'Abnormal eye morphology'),
(32894, 'HP:0000589', 'Coloboma', 'XPO:0103101', 'abnormal medial nasal prominence morphology', 0.4375, 4.5318002188002176, 1.4080705222839853, 'UPHENO:0087907', 'abnormal head morphology'),
(32895, 'HP:0000589', 'Coloboma', 'XPO:0115526', 'abnormally incomplete structure of head', 0.45652173913043476, 4.5318002188002176, 1.4383550734357495, 'UPHENO:0087907', 'abnormal head morphology'),
(32896, 'HP:0000589', 'Coloboma', 'XPO:0133369', 'eye fused with brain', 0.4696969696969697, 6.887869297006056, 1.7986693238259617, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(32897, 'HP:0000589', 'Coloboma', 'XPO:0130122', 'increased size of the retinal layer', 0.41333333333333333, 6.887869297006056, 1.6873013886368484, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(32898, 'HP:0000589', 'Coloboma', 'XPO:0141339', 'decreased pigmentation in the head', 0.4375, 4.5318002188002176, 1.4080705222839853, 'UPHENO:0087907', 'abnormal head morphology'),
(32899, 'HP:0000589', 'Coloboma', 'XPO:0115417', 'abnormally wholly ventralized eye', 0.44285714285714284, 6.887869297006056, 1.7465228647932265, 'HP:0012372', 'Abnormal eye morphology'),
(32900, 'HP:0000589', 'Coloboma', 'XPO:0101634', 'abnormal head morphology', 0.4666666666666667, 4.5318002188002176, 1.4542489821577214, 'UPHENO:0087907', 'abnormal head morphology'),
(32901, 'HP:0000589', 'Coloboma', 'XPO:0139731', 'abnormally necrotic eye', 0.44285714285714284, 6.887869297006056, 1.7465228647932265, 'HP:0012372', 'Abnormal eye morphology'),
(32902, 'HP:0000589', 'Coloboma', 'XPO:0100779', 'abnormal optic choroid vascular plexus', 0.5535714285714286, 6.887869297006056, 1.9526719249676645, 'HP:0012372', 'Abnormal eye morphology'),
(32903, 'HP:0000589', 'Coloboma', 'XPO:0102947', 'abnormal hyaloid vascular plexus morphology', 0.41333333333333333, 6.887869297006056, 1.6873013886368484, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(32904, 'HP:0000589', 'Coloboma', 'XPO:0102804', 'abnormal pharyngeal pouch morphology', 0.4375, 4.5318002188002176, 1.4080705222839853, 'UPHENO:0087907', 'abnormal head morphology'),
(32905, 'HP:0000589', 'Coloboma', 'XPO:0139715', 'abnormally necrotic head', 0.42, 4.5318002188002176, 1.3796217205799897, 'UPHENO:0087907', 'abnormal head morphology'),
(32906, 'HP:0000589', 'Coloboma', 'XPO:0141298', 'abnormal intercanthal region morphology', 0.44680851063829785, 4.5318002188002176, 1.422971154406314, 'UPHENO:0087907', 'abnormal head morphology'),
(32907, 'HP:0000589', 'Coloboma', 'XPO:0140668', 'abnormally necrotic medial nasal prominence', 0.40384615384615385, 4.5318002188002176, 1.3528303989641963, 'UPHENO:0087907', 'abnormal head morphology'),
(32908, 'HP:0000589', 'Coloboma', 'XPO:0128467', 'decreased size of the lens', 0.41333333333333333, 6.887869297006056, 1.6873013886368484, 'HP:0012372', 'Abnormal eye morphology'),
(32909, 'HP:0000589', 'Coloboma', 'XPO:0140799', 'abnormally necrotic ciliary body', 0.4025974025974026, 6.887869297006056, 1.6652442128423794, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(32910, 'HP:0000589', 'Coloboma', 'XPO:0141638', 'neoplastic eye', 0.4696969696969697, 6.887869297006056, 1.7986693238259617, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(32911, 'HP:0000589', 'Coloboma', 'XPO:0140335', 'abnormally necrotic pharyngeal region', 0.44680851063829785, 4.5318002188002176, 1.422971154406314, 'UPHENO:0087907', 'abnormal head morphology'),
(32912, 'HP:0000589', 'Coloboma', 'XPO:0140820', 'abnormally necrotic globe', 0.40298507462686567, 6.575878401988876, 1.6278761772821302, 'UPHENO:0087924', 'abnormal camera-type eye morphology'),
(32913, 'HP:0000589', 'Coloboma', 'XPO:0103707', 'increased pigmentation in the head', 0.4375, 4.5318002188002176, 1.4080705222839853, 'UPHENO:0087907', 'abnormal head morphology'),
(32914, 'HP:0000589', 'Coloboma', 'XPO:0101483', 'abnormal nostril', 0.47058823529411764, 5.788671267106304, 1.6504788990730295, 'UPHENO:0087472', 'abnormal face morphology'),
(32915, 'HP:0000589', 'Coloboma', 'XPO:0141323', 'edematous eye', 0.47692307692307695, 6.887869297006056, 1.8124524320853552, 'HP:0012372', 'Abnormal eye morphology'),
(32916, 'HP:0000589', 'Coloboma', 'XPO:0102550', 'abnormal lens morphology', 0.4626865671641791, 6.887869297006056, 1.7851959556606887, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(32917, 'HP:0000589', 'Coloboma', 'XPO:0103160', 'abnormal choroid morphology', 0.421875, 6.575878401988876, 1.6655925974976766, 'UPHENO:0087924', 'abnormal camera-type eye morphology'),
(32918, 'HP:0000589', 'Coloboma', 'XPO:0133354', 'fused eyes', 0.4696969696969697, 6.887869297006056, 1.7986693238259617, 'HP:0012372', 'Abnormal eye morphology'),
(32919, 'HP:0000589', 'Coloboma', 'XPO:0103115', 'abnormal nostril morphology', 0.4067796610169492, 5.788671267106304, 1.5345076525622334, 'UPHENO:0087472', 'abnormal face morphology'),
(32920, 'HP:0000589', 'Coloboma', 'XPO:0102003', 'abnormal hyaloid blood vessel morphology', 0.45588235294117646, 6.887869297006056, 1.7720208976957377, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(32921, 'HP:0000589', 'Coloboma', 'XPO:0133370', 'olfactory pit fused with brain', 0.4067796610169492, 5.788671267106304, 1.5345076525622334, 'UPHENO:0087472', 'abnormal face morphology'),
(32922, 'HP:0000589', 'Coloboma', 'XPO:0127907', 'abnormally localised optic choroid vascular plexus', 0.4626865671641791, 6.887869297006056, 1.7851959556606887, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(32923, 'HP:0000589', 'Coloboma', 'XPO:0102734', 'abnormal craniofacial region morphology', 0.4375, 4.5318002188002176, 1.4080705222839853, 'UPHENO:0087907', 'abnormal head morphology'),
(32924, 'HP:0000589', 'Coloboma', 'XPO:0101315', 'abnormal hyaloid vascular plexus', 0.543859649122807, 6.887869297006056, 1.9354674316747025, 'HP:0012372', 'Abnormal eye morphology'),
(32925, 'HP:0000589', 'Coloboma', 'XPO:0102513', 'abnormal sclera morphology', 0.484375, 6.887869297006056, 1.8265573330003382, 'HP:0012372', 'Abnormal eye morphology'),
(32926, 'HP:0000589', 'Coloboma', 'XPO:0102117', 'abnormal retina morphology', 0.44285714285714284, 6.887869297006056, 1.7465228647932265, 'HP:0012372', 'Abnormal eye morphology'),
(32927, 'HP:0000589', 'Coloboma', 'XPO:0127645', 'abnormally localised hyaloid vein', 0.45588235294117646, 6.887869297006056, 1.7720208976957377, 'HP:0012372', 'Abnormal eye morphology'),
(32928, 'HP:0000589', 'Coloboma', 'XPO:0140473', 'abnormally necrotic lens transitional zone', 0.4189189189189189, 6.887869297006056, 1.6986638159319787, 'HP:0012372', 'Abnormal eye morphology'),
(32929, 'HP:0000589', 'Coloboma', 'XPO:0128300', 'decreased size of the retina', 0.4025974025974026, 6.887869297006056, 1.6652442128423794, 'HP:0012372', 'Abnormal eye morphology'),
(32930, 'HP:0000589', 'Coloboma', 'XPO:0102572', 'abnormal hatching gland primordium morphology', 0.42, 4.5318002188002176, 1.3796217205799897, 'UPHENO:0087907', 'abnormal head morphology'),
(32931, 'HP:0000589', 'Coloboma', 'XPO:0142059', 'abnormal nasal region morphology', 0.45652173913043476, 4.5318002188002176, 1.4383550734357495, 'UPHENO:0087907', 'abnormal head morphology'),
(32932, 'HP:0000589', 'Coloboma', 'XPO:0102476', 'abnormal lens transitional zone morphology', 0.4492753623188406, 6.887869297006056, 1.759133301946505, 'HP:0012372', 'Abnormal eye morphology'),
(32933, 'HP:0000589', 'Coloboma', 'XPO:0103186', 'abnormal peripheral retina morphology', 0.4246575342465753, 6.887869297006056, 1.7102589253909142, 'HP:0012372', 'Abnormal eye morphology'),
(32934, 'HP:0000589', 'Coloboma', 'XPO:0126243', 'absent optic choroid vascular plexus', 0.4305555555555556, 6.887869297006056, 1.7220947685207388, 'HP:0012372', 'Abnormal eye morphology'),
(32935, 'HP:0000589', 'Coloboma', 'XPO:0128568', 'decreased size of the optic disc', 0.4153846153846154, 6.575878401988876, 1.652730686114997, 'UPHENO:0087924', 'abnormal camera-type eye morphology'),
(32936, 'HP:0000589', 'Coloboma', 'XPO:0131600', 'decreased size of the intercanthal region', 0.40384615384615385, 4.5318002188002176, 1.3528303989641963, 'UPHENO:0087907', 'abnormal head morphology'),
(32937, 'HP:0000589', 'Coloboma', 'XPO:0102505', 'abnormal retinal stem cell region morphology', 0.4189189189189189, 6.887869297006056, 1.6986638159319787, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(32938, 'HP:0000589', 'Coloboma', 'XPO:0141343', 'decreased pigmentation in the eye', 0.4696969696969697, 6.887869297006056, 1.7986693238259617, 'HP:0012372', 'Abnormal eye morphology'),
(32939, 'HP:0000589', 'Coloboma', 'XPO:0141839', 'edematous pharyngeal region', 0.45652173913043476, 4.5318002188002176, 1.4383550734357495, 'UPHENO:0087907', 'abnormal head morphology'),
(32940, 'HP:0000589', 'Coloboma', 'XPO:0133371', 'eye fused with olfactory pit', 0.4696969696969697, 6.887869297006056, 1.7986693238259617, 'HP:0012372', 'Abnormal eye morphology'),
(32941, 'HP:0000589', 'Coloboma', 'XPO:0100420', 'abnormal choana', 0.4528301886792453, 5.788671267106304, 1.6190383263177786, 'UPHENO:0087472', 'abnormal face morphology'),
(32942, 'HP:0000589', 'Coloboma', 'XPO:0141835', 'edematous head', 0.44680851063829785, 4.5318002188002176, 1.422971154406314, 'UPHENO:0087907', 'abnormal head morphology'),
(32943, 'HP:0000589', 'Coloboma', 'XPO:0103376', 'increased size of the eye', 0.4189189189189189, 6.887869297006056, 1.6986638159319787, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(32944, 'HP:0000589', 'Coloboma', 'XPO:0140192', 'abnormally necrotic retina', 0.41333333333333333, 6.887869297006056, 1.6873013886368484, 'HP:0012372', 'Abnormal eye morphology'),
(32945, 'HP:0000589', 'Coloboma', 'XPO:0139722', 'abnormally necrotic hyaloid blood vessel', 0.4189189189189189, 6.887869297006056, 1.6986638159319787, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(32946, 'HP:0000589', 'Coloboma', 'XPO:0115423', 'abnormally incomplete structure of eye', 0.484375, 6.887869297006056, 1.8265573330003382, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(32947, 'HP:0000589', 'Coloboma', 'XPO:0127230', 'abnormally localised hyaloid blood vessel', 0.484375, 6.887869297006056, 1.8265573330003382, 'HP:0012372', 'Abnormal eye morphology'),
(32948, 'HP:0000589', 'Coloboma', 'XPO:0129780', 'increased size of the retina', 0.4025974025974026, 6.887869297006056, 1.6652442128423794, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(32949, 'HP:0000589', 'Coloboma', 'XPO:0128564', 'decreased size of the hyaloid blood vessel', 0.40789473684210525, 6.887869297006056, 1.6761639640277146, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(32950, 'HP:0000589', 'Coloboma', 'XPO:0130048', 'increased size of the optic disc', 0.4153846153846154, 6.575878401988876, 1.652730686114997, 'UPHENO:0087924', 'abnormal camera-type eye morphology'),
(32951, 'HP:0000589', 'Coloboma', 'XPO:0130044', 'increased size of the hyaloid blood vessel', 0.40789473684210525, 6.887869297006056, 1.6761639640277146, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(32952, 'HP:0000589', 'Coloboma', 'XPO:0102966', 'abnormal olfactory pit morphology', 0.42857142857142855, 5.788671267106304, 1.5750743203017852, 'UPHENO:0087472', 'abnormal face morphology'),
(32953, 'HP:0000589', 'Coloboma', 'XPO:0102831', 'abnormal optic disc morphology', 0.45, 6.575878401988876, 1.7202166377799613, 'UPHENO:0087924', 'abnormal camera-type eye morphology'),
(32954, 'HP:0000589', 'Coloboma', 'XPO:0102212', 'abnormal globe morphology', 0.43548387096774194, 6.575878401988876, 1.692243771302257, 'UPHENO:0087924', 'abnormal camera-type eye morphology'),
(32955, 'HP:0000589', 'Coloboma', 'XPO:0140017', 'abnormally necrotic lateral nasal prominence', 0.40384615384615385, 4.5318002188002176, 1.3528303989641963, 'UPHENO:0087907', 'abnormal head morphology'),
(32956, 'HP:0000589', 'Coloboma', 'XPO:0128582', 'decreased size of the head region', 0.40384615384615385, 4.5318002188002176, 1.3528303989641963, 'UPHENO:0087907', 'abnormal head morphology'),
(32957, 'HP:0000589', 'Coloboma', 'XPO:0141141', 'abnormally necrotic cornea', 0.4025974025974026, 6.887869297006056, 1.6652442128423794, 'HP:0012372', 'Abnormal eye morphology'),
(32958, 'HP:0000589', 'Coloboma', 'XPO:0102259', 'abnormal pharyngeal region morphology', 0.4772727272727273, 4.5318002188002176, 1.4706816956370683, 'UPHENO:0087907', 'abnormal head morphology'),
(32959, 'HP:0000589', 'Coloboma', 'XPO:0102342', 'abnormal hyaloid vein morphology', 0.40789473684210525, 6.887869297006056, 1.6761639640277146, 'HP:0012372', 'Abnormal eye morphology'),
(32960, 'HP:0000589', 'Coloboma', 'XPO:0140914', 'abnormally necrotic intercanthal region', 0.42, 4.5318002188002176, 1.3796217205799897, 'UPHENO:0087907', 'abnormal head morphology'),
(32961, 'HP:0000589', 'Coloboma', 'XPO:0103022', 'abnormal ciliary body morphology', 0.43661971830985913, 6.887869297006056, 1.734179792355427, 'HP:0012372', 'Abnormal eye morphology'),
(32962, 'HP:0000589', 'Coloboma', 'XPO:0129947', 'increased size of the lens', 0.41333333333333333, 6.887869297006056, 1.6873013886368484, 'HP:0012372', 'Abnormal eye morphology'),
(32963, 'HP:0000589', 'Coloboma', 'XPO:0126122', 'absent hyaloid vascular plexus', 0.4305555555555556, 6.887869297006056, 1.7220947685207388, 'HP:0012372', 'Abnormal eye morphology'),
(32964, 'HP:0000589', 'Coloboma', 'XPO:0131638', 'increased size of the intercanthal region', 0.40384615384615385, 4.5318002188002176, 1.3528303989641963, 'UPHENO:0087907', 'abnormal head morphology'),
(32965, 'HP:0000589', 'Coloboma', 'XPO:0129388', 'decreased size of the sclera', 0.43661971830985913, 6.887869297006056, 1.734179792355427, 'HP:0012372', 'Abnormal eye morphology'),
(32966, 'HP:0000589', 'Coloboma', 'XPO:0133372', 'eye fused with olfactory epithelium', 0.4696969696969697, 6.887869297006056, 1.7986693238259617, 'HP:0012372', 'Abnormal eye morphology'),
(32967, 'HP:0000589', 'Coloboma', 'XPO:0101823', 'abnormal lens epithelium morphology', 0.40789473684210525, 6.887869297006056, 1.6761639640277146, 'HP:0012372', 'Abnormal eye morphology'),
(32968, 'HP:0000589', 'Coloboma', 'XPO:0100329', 'abnormal retinal blood vessel', 0.4492753623188406, 6.887869297006056, 1.759133301946505, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(32969, 'HP:0000589', 'Coloboma', 'XPO:0140223', 'abnormally necrotic head region', 0.42, 4.5318002188002176, 1.3796217205799897, 'UPHENO:0087907', 'abnormal head morphology'),
(32970, 'HP:0000589', 'Coloboma', 'XPO:0101173', 'abnormal retinal layer', 0.42, 6.02624522851634, 1.590918915588366, 'HP:0000478', 'Abnormality of the eye'),
(32971, 'HP:0000589', 'Coloboma', 'XPO:0103336', 'decreased size of the eye', 0.4189189189189189, 6.887869297006056, 1.6986638159319787, 'HP:0012372', 'Abnormal eye morphology'),
(32972, 'HP:0000589', 'Coloboma', 'XPO:0140391', 'abnormally necrotic central retina', 0.4246575342465753, 6.887869297006056, 1.7102589253909142, 'HP:0012372', 'Abnormal eye morphology'),
(32973, 'HP:0000589', 'Coloboma', 'XPO:0102082', 'abnormal circumpharyngeal ridge morphology', 0.42857142857142855, 4.5318002188002176, 1.3936283915633758, 'UPHENO:0087907', 'abnormal head morphology'),
(32974, 'HP:0000589', 'Coloboma', 'XPO:0130863', 'increased size of the sclera', 0.43661971830985913, 6.887869297006056, 1.734179792355427, 'HP:0012372', 'Abnormal eye morphology'),
(32975, 'HP:0000589', 'Coloboma', 'XPO:0100710', 'abnormal hyaloid vein', 0.543859649122807, 6.887869297006056, 1.9354674316747025, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(32976, 'HP:0000589', 'Coloboma', 'XPO:0101359', 'abnormal hyaloid artery', 0.43661971830985913, 6.887869297006056, 1.734179792355427, 'HP:0012372', 'Abnormal eye morphology'),
(32977, 'HP:0000589', 'Coloboma', 'XPO:0125589', 'absent hyaloid blood vessel', 0.4626865671641791, 6.887869297006056, 1.7851959556606887, 'HP:0012372', 'Abnormal eye morphology'),
(32978, 'HP:0000589', 'Coloboma', 'XPO:0103739', 'increased size of the pharyngeal region', 0.42857142857142855, 4.5318002188002176, 1.3936283915633758, 'UPHENO:0087907', 'abnormal head morphology'),
(32979, 'HP:0000589', 'Coloboma', 'XPO:0103048', 'abnormal cornea morphology', 0.43661971830985913, 6.887869297006056, 1.734179792355427, 'HP:0012372', 'Abnormal eye morphology'),
(32980, 'HP:0000589', 'Coloboma', 'XPO:0128935', 'decreased size of the central retina', 0.41333333333333333, 6.887869297006056, 1.6873013886368484, 'HP:0012372', 'Abnormal eye morphology'),
(32981, 'HP:0000589', 'Coloboma', 'XPO:0102538', 'abnormal lateral nasal prominence morphology', 0.4375, 4.5318002188002176, 1.4080705222839853, 'UPHENO:0087907', 'abnormal head morphology'),
(32982, 'HP:0000589', 'Coloboma', 'XPO:0127783', 'abnormally localised hyaloid vascular plexus', 0.4492753623188406, 6.887869297006056, 1.759133301946505, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(32983, 'HP:0000589', 'Coloboma', 'XPO:0140553', 'abnormally necrotic retinal stem cell region', 0.4025974025974026, 6.887869297006056, 1.6652442128423794, 'HP:0012372', 'Abnormal eye morphology'),
(32984, 'HP:0000589', 'Coloboma', 'XPO:0128643', 'decreased size of the retinal layer', 0.41333333333333333, 6.887869297006056, 1.6873013886368484, 'HP:0012372', 'Abnormal eye morphology'),
(32985, 'HP:0000589', 'Coloboma', 'XPO:0140538', 'abnormally necrotic optic disc', 0.42857142857142855, 6.575878401988876, 1.6787595422967447, 'UPHENO:0087924', 'abnormal camera-type eye morphology'),
(32986, 'HP:0000589', 'Coloboma', 'XPO:0128807', 'decreased size of the lens transitional zone', 0.40789473684210525, 6.887869297006056, 1.6761639640277146, 'HP:0012372', 'Abnormal eye morphology'),
(32987, 'HP:0000589', 'Coloboma', 'XPO:0102784', 'abnormal retinal progenitor cell region morphology', 0.4189189189189189, 6.887869297006056, 1.6986638159319787, 'HP:0012372', 'Abnormal eye morphology'),
(32988, 'HP:0000589', 'Coloboma', 'XPO:0140375', 'abnormally necrotic lens', 0.4305555555555556, 6.887869297006056, 1.7220947685207388, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(32989, 'HP:0000589', 'Coloboma', 'XPO:0102805', 'abnormal retinal layer morphology', 0.45588235294117646, 6.887869297006056, 1.7720208976957377, 'HP:0012372', 'Abnormal eye morphology'),
(32990, 'HP:0000589', 'Coloboma', 'XPO:0140218', 'abnormally necrotic sclera', 0.4492753623188406, 6.887869297006056, 1.759133301946505, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(32991, 'HP:0000589', 'Coloboma', 'XPO:0100371', 'abnormal hyaloid blood vessel', 0.5636363636363636, 6.887869297006056, 1.9703435243040868, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(32992, 'HP:0002592', 'Gastric ulcer', 'XPO:0102403', 'abnormal distal stomach morphology', 0.4032258064516129, 10.57542522308115, 2.065014373835113, 'HP:0002577', 'Abnormal stomach morphology'),
(32993, 'HP:0002592', 'Gastric ulcer', 'XPO:0101788', 'abnormal foregut morphology', 0.40425531914893614, 7.748525470353617, 1.7698538462120148, 'UPHENO:0087359', 'abnormal foregut morphology'),
(32994, 'HP:0002592', 'Gastric ulcer', 'XPO:0101784', 'abnormal alimentary system morphology', 0.4090909090909091, 5.725717590856133, 1.5304701939081158, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(32995, 'HP:0002592', 'Gastric ulcer', 'XPO:0102522', 'abnormal pharyngeal cavity morphology', 0.4090909090909091, 5.725717590856133, 1.5304701939081158, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(32996, 'HP:0002592', 'Gastric ulcer', 'XPO:0102023', 'abnormal proximal stomach morphology', 0.4032258064516129, 10.57542522308115, 2.065014373835113, 'HP:0002577', 'Abnormal stomach morphology'),
(32997, 'HP:0002592', 'Gastric ulcer', 'XPO:0100152', 'abnormal alimentary system', 0.40540540540540543, 5.05060299610679, 1.4309233924911664, 'HP:0025031', 'Abnormality of the digestive system'),
(32998, 'HP:0002592', 'Gastric ulcer', 'XPO:0100361', 'abnormal small intestine', 0.4074074074074074, 8.037124161124119, 1.809525881963287, 'UPHENO:0076735', 'abnormal alimentary part of gastrointestinal system morphology'),
(32999, 'HP:0031803', 'Fundus hemorrhage', 'XPO:0102162', 'abnormal ciliary marginal zone morphology', 0.40217391304347827, 7.796308075334707, 1.7707263272312377, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(33000, 'HP:0031803', 'Fundus hemorrhage', 'XPO:0101315', 'abnormal hyaloid vascular plexus', 0.44, 6.887869297006056, 1.7408798036288045, 'HP:0012372', 'Abnormal eye morphology'),
(33001, 'HP:0031803', 'Fundus hemorrhage', 'XPO:0100371', 'abnormal hyaloid blood vessel', 0.4520547945205479, 6.887869297006056, 1.7645663319191103, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(33002, 'HP:0031803', 'Fundus hemorrhage', 'XPO:0100329', 'abnormal retinal blood vessel', 0.48148148148148145, 7.796308075334707, 1.9374668931876466, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(33003, 'HP:0031803', 'Fundus hemorrhage', 'XPO:0127230', 'abnormally localised hyaloid blood vessel', 0.4024390243902439, 6.887869297006056, 1.6649166345540045, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(33004, 'HP:0031803', 'Fundus hemorrhage', 'XPO:0128935', 'decreased size of the central retina', 0.4157303370786517, 7.796308075334707, 1.8003226888888313, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(33005, 'HP:0031803', 'Fundus hemorrhage', 'XPO:0103186', 'abnormal peripheral retina morphology', 0.42528735632183906, 7.796308075334707, 1.8208984733997946, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(33006, 'HP:0031803', 'Fundus hemorrhage', 'XPO:0102505', 'abnormal retinal stem cell region morphology', 0.42045454545454547, 7.796308075334707, 1.8105228990649238, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(33007, 'HP:0031803', 'Fundus hemorrhage', 'XPO:0140553', 'abnormally necrotic retinal stem cell region', 0.4065934065934066, 7.796308075334707, 1.7804290098743123, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(33008, 'HP:0031803', 'Fundus hemorrhage', 'XPO:0100710', 'abnormal hyaloid vein', 0.44, 6.887869297006056, 1.7408798036288045, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(33009, 'HP:0031803', 'Fundus hemorrhage', 'XPO:0102756', 'abnormal Muller cell morphology', 0.40217391304347827, 7.796308075334707, 1.7707263272312377, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(33010, 'HP:0031803', 'Fundus hemorrhage', 'XPO:0140391', 'abnormally necrotic central retina', 0.42528735632183906, 7.796308075334707, 1.8208984733997946, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(33011, 'HP:0031803', 'Fundus hemorrhage', 'XPO:0102196', 'abnormal central retina morphology', 0.44047619047619047, 7.796308075334707, 1.8531292671592536, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(33012, 'HP:0031803', 'Fundus hemorrhage', 'XPO:0128643', 'decreased size of the retinal layer', 0.4157303370786517, 7.796308075334707, 1.8003226888888313, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(33013, 'HP:0031803', 'Fundus hemorrhage', 'XPO:0125909', 'absent retinal blood vessel', 0.40625, 7.796308075334707, 1.7796769806919246, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(33014, 'HP:0031803', 'Fundus hemorrhage', 'XPO:0127563', 'abnormally localised retinal blood vessel', 0.42857142857142855, 7.796308075334707, 1.8279154492014011, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(33015, 'HP:0031803', 'Fundus hemorrhage', 'XPO:0140192', 'abnormally necrotic retina', 0.4157303370786517, 7.796308075334707, 1.8003226888888313, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(33016, 'HP:0031803', 'Fundus hemorrhage', 'XPO:0140487', 'abnormally necrotic retinal layer', 0.42045454545454547, 7.796308075334707, 1.8105228990649238, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(33017, 'HP:0031803', 'Fundus hemorrhage', 'XPO:0128300', 'decreased size of the retina', 0.4065934065934066, 7.796308075334707, 1.7804290098743123, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(33018, 'HP:0031803', 'Fundus hemorrhage', 'XPO:0102784', 'abnormal retinal progenitor cell region morphology', 0.42045454545454547, 7.796308075334707, 1.8105228990649238, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(33019, 'HP:0031803', 'Fundus hemorrhage', 'XPO:0130122', 'increased size of the retinal layer', 0.4157303370786517, 7.796308075334707, 1.8003226888888313, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(33020, 'HP:0031803', 'Fundus hemorrhage', 'XPO:0102411', 'abnormal optic choroid vascular plexus morphology', 0.40625, 7.796308075334707, 1.7796769806919246, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(33021, 'HP:0031803', 'Fundus hemorrhage', 'XPO:0102117', 'abnormal retina morphology', 0.44047619047619047, 7.796308075334707, 1.8531292671592536, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(33022, 'HP:0031803', 'Fundus hemorrhage', 'XPO:0140531', 'abnormally necrotic retinal progenitor cell region', 0.4065934065934066, 7.796308075334707, 1.7804290098743123, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(33023, 'HP:0031803', 'Fundus hemorrhage', 'XPO:0100779', 'abnormal optic choroid vascular plexus', 0.44594594594594594, 6.887869297006056, 1.7526030324079105, 'HP:0012372', 'Abnormal eye morphology'),
(33024, 'HP:0031803', 'Fundus hemorrhage', 'XPO:0129780', 'increased size of the retina', 0.4065934065934066, 7.796308075334707, 1.7804290098743123, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(33025, 'HP:0031803', 'Fundus hemorrhage', 'XPO:0102805', 'abnormal retinal layer morphology', 0.45121951219512196, 7.796308075334707, 1.8755922602408597, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(33026, 'HP:0031803', 'Fundus hemorrhage', 'XPO:0130413', 'increased size of the central retina', 0.4157303370786517, 7.796308075334707, 1.8003226888888313, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(33027, 'HP:0006705', 'Abnormal atrioventricular valve morphology', 'XPO:0141283', 'abnormal atrioventricular valve morphology', 0.43137254901960786, 7.90143706196527, 1.8462023308234556, 'UPHENO:0015324', 'abnormal anatomical entity morphology in the heart'),
(33028, 'HP:0006705', 'Abnormal atrioventricular valve morphology', 'XPO:0101976', 'abnormal portion of organism substance morphology', 0.43333333333333335, 2.786899518863159, 1.0989342374200721, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(33029, 'HP:0006705', 'Abnormal atrioventricular valve morphology', 'XPO:0101900', 'abnormal circulatory system morphology', 0.5, 5.9590888072311134, 1.7261356851694936, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(33030, 'HP:0006705', 'Abnormal atrioventricular valve morphology', 'XPO:0101638', 'abnormal anatomical structure morphology', 0.43333333333333335, 2.786899518863159, 1.0989342374200721, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(33031, 'HP:0006705', 'Abnormal atrioventricular valve morphology', 'XPO:0102649', 'abnormal outflow tract morphology', 0.44, 7.90143706196527, 1.8645729557367068, 'UPHENO:0015324', 'abnormal anatomical entity morphology in the heart'),
(33032, 'HP:0006705', 'Abnormal atrioventricular valve morphology', 'XPO:0140144', 'abnormally necrotic portion of organism substance', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(33033, 'HP:0006705', 'Abnormal atrioventricular valve morphology', 'XPO:0140269', 'abnormally necrotic anatomical line', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(33034, 'HP:0006705', 'Abnormal atrioventricular valve morphology', 'XPO:0140420', 'abnormally necrotic bulbous arteriosis', 0.41304347826086957, 5.9590888072311134, 1.5688730886225806, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(33035, 'HP:0006705', 'Abnormal atrioventricular valve morphology', 'XPO:0101995', 'abnormal cardiovascular system morphology', 0.5, 5.9590888072311134, 1.7261356851694936, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(33036, 'HP:0006705', 'Abnormal atrioventricular valve morphology', 'XPO:0139990', 'abnormally necrotic cardiovascular system', 0.4318181818181818, 5.9590888072311134, 1.6041330661860995, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(33037, 'HP:0006705', 'Abnormal atrioventricular valve morphology', 'XPO:0129679', 'increased size of the cardiac valve', 0.4482758620689655, 10.21769640676594, 2.140174447352826, 'UPHENO:0015319', 'abnormal cardiac valve morphology in the heart'),
(33038, 'HP:0006705', 'Abnormal atrioventricular valve morphology', 'XPO:0102769', 'abnormal cardiac valve morphology', 0.5098039215686274, 10.21769640676594, 2.2823281310028474, 'UPHENO:0015319', 'abnormal cardiac valve morphology in the heart'),
(33039, 'HP:0006705', 'Abnormal atrioventricular valve morphology', 'XPO:0102742', 'abnormal cell-free extract morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(33040, 'HP:0006705', 'Abnormal atrioventricular valve morphology', 'XPO:0129961', 'increased size of the circulatory system', 0.41304347826086957, 5.9590888072311134, 1.5688730886225806, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(33041, 'HP:0006705', 'Abnormal atrioventricular valve morphology', 'XPO:0101694', 'abnormal anatomical space morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(33042, 'HP:0006705', 'Abnormal atrioventricular valve morphology', 'XPO:0102460', 'abnormal atrioventricular valve leaflet morphology', 0.4230769230769231, 7.90143706196527, 1.8283642088113161, 'UPHENO:0015324', 'abnormal anatomical entity morphology in the heart'),
(33043, 'HP:0006705', 'Abnormal atrioventricular valve morphology', 'XPO:0100837', 'abnormal atrioventricular canal', 0.41509433962264153, 7.90143706196527, 1.8110333512407601, 'UPHENO:0015324', 'abnormal anatomical entity morphology in the heart'),
(33044, 'HP:0006705', 'Abnormal atrioventricular valve morphology', 'XPO:0101891', 'abnormal endocardium morphology', 0.4074074074074074, 7.90143706196527, 1.7941861631971396, 'UPHENO:0015324', 'abnormal anatomical entity morphology in the heart'),
(33045, 'HP:0006705', 'Abnormal atrioventricular valve morphology', 'XPO:0101740', 'abnormal cell part morphology', 0.4166666666666667, 2.786899518863159, 1.0775936770692605, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(33046, 'HP:0006705', 'Abnormal atrioventricular valve morphology', 'XPO:0102751', 'abnormal trabecula carnea morphology', 0.41509433962264153, 7.90143706196527, 1.8110333512407601, 'UPHENO:0015324', 'abnormal anatomical entity morphology in the heart'),
(33047, 'HP:0006705', 'Abnormal atrioventricular valve morphology', 'XPO:0107345', 'abnormal anatomical axis morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(33048, 'HP:0006705', 'Abnormal atrioventricular valve morphology', 'XPO:0103024', 'abnormal sinus venosus morphology', 0.44, 7.90143706196527, 1.8645729557367068, 'UPHENO:0015324', 'abnormal anatomical entity morphology in the heart'),
(33049, 'HP:0006705', 'Abnormal atrioventricular valve morphology', 'XPO:0102532', 'abnormal angioblast morphology', 0.4418604651162791, 5.9590888072311134, 1.6226785732338835, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(33050, 'HP:0006705', 'Abnormal atrioventricular valve morphology', 'XPO:0102800', 'abnormal circulating cell morphology', 0.4418604651162791, 5.9590888072311134, 1.6226785732338835, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(33051, 'HP:0006705', 'Abnormal atrioventricular valve morphology', 'XPO:0101686', 'abnormal blood vessel morphology', 0.41304347826086957, 5.9590888072311134, 1.5688730886225806, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(33052, 'HP:0006705', 'Abnormal atrioventricular valve morphology', 'XPO:0101713', 'abnormal anatomical entity in vitro morphology', 0.43333333333333335, 2.786899518863159, 1.0989342374200721, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(33053, 'HP:0006705', 'Abnormal atrioventricular valve morphology', 'XPO:0102601', 'abnormal disaggregated/reaggregated ectoderm treated with activin morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(33054, 'HP:0006705', 'Abnormal atrioventricular valve morphology', 'XPO:0102935', 'abnormal bulbous arteriosis morphology', 0.4634146341463415, 5.9590888072311134, 1.6617848715909544, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(33055, 'HP:0006705', 'Abnormal atrioventricular valve morphology', 'XPO:0139718', 'abnormally necrotic anatomical structure', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(33056, 'HP:0006705', 'Abnormal atrioventricular valve morphology', 'XPO:0141112', 'abnormally necrotic angioblast', 0.40425531914893614, 5.9590888072311134, 1.552093214856655, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(33057, 'HP:0006705', 'Abnormal atrioventricular valve morphology', 'XPO:0101636', 'abnormal cell morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(33058, 'HP:0006705', 'Abnormal atrioventricular valve morphology', 'XPO:0128032', 'decreased size of the cardiovascular system', 0.41304347826086957, 5.9590888072311134, 1.5688730886225806, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(33059, 'HP:0006705', 'Abnormal atrioventricular valve morphology', 'XPO:0141328', 'edematous circulatory system', 0.4634146341463415, 5.9590888072311134, 1.6617848715909544, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(33060, 'HP:0006705', 'Abnormal atrioventricular valve morphology', 'XPO:0102178', 'abnormal whole organism morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(33061, 'HP:0006705', 'Abnormal atrioventricular valve morphology', 'XPO:0141316', 'abnormal anatomical region morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(33062, 'HP:0006705', 'Abnormal atrioventricular valve morphology', 'XPO:0101890', 'abnormal organ part morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(33063, 'HP:0006705', 'Abnormal atrioventricular valve morphology', 'XPO:0101919', 'abnormal heart primordium morphology', 0.4418604651162791, 5.9590888072311134, 1.6226785732338835, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(33064, 'HP:0006705', 'Abnormal atrioventricular valve morphology', 'XPO:0141220', 'abnormally necrotic cardiac valve', 0.4642857142857143, 10.21769640676594, 2.17805658204049, 'UPHENO:0015319', 'abnormal cardiac valve morphology in the heart'),
(33065, 'HP:0006705', 'Abnormal atrioventricular valve morphology', 'XPO:0102773', 'abnormal Keller explant morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(33066, 'HP:0006705', 'Abnormal atrioventricular valve morphology', 'XPO:0139811', 'abnormally necrotic circulatory system', 0.4318181818181818, 5.9590888072311134, 1.6041330661860995, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(33067, 'HP:0006705', 'Abnormal atrioventricular valve morphology', 'XPO:0103124', 'abnormal atrial septum morphology', 0.41509433962264153, 7.90143706196527, 1.8110333512407601, 'UPHENO:0015324', 'abnormal anatomical entity morphology in the heart'),
(33068, 'HP:0006705', 'Abnormal atrioventricular valve morphology', 'XPO:0103201', 'abnormal activin-induced ectoderm morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(33069, 'HP:0006705', 'Abnormal atrioventricular valve morphology', 'XPO:0128481', 'decreased size of the circulatory system', 0.41304347826086957, 5.9590888072311134, 1.5688730886225806, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(33070, 'HP:0006705', 'Abnormal atrioventricular valve morphology', 'XPO:0140104', 'abnormally necrotic circulating cell', 0.40425531914893614, 5.9590888072311134, 1.552093214856655, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(33071, 'HP:0006705', 'Abnormal atrioventricular valve morphology', 'XPO:0101770', 'abnormal trunk vasculature morphology', 0.4222222222222222, 5.9590888072311134, 1.5862092291399303, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(33072, 'HP:0006705', 'Abnormal atrioventricular valve morphology', 'XPO:0128199', 'decreased size of the cardiac valve', 0.4482758620689655, 10.21769640676594, 2.140174447352826, 'UPHENO:0015319', 'abnormal cardiac valve morphology in the heart'),
(33073, 'HP:0006705', 'Abnormal atrioventricular valve morphology', 'XPO:0107343', 'abnormal cardiac atrium morphology', 0.4230769230769231, 7.90143706196527, 1.8283642088113161, 'UPHENO:0015324', 'abnormal anatomical entity morphology in the heart'),
(33074, 'HP:0006705', 'Abnormal atrioventricular valve morphology', 'XPO:0102113', 'abnormal anatomical line morphology', 0.43333333333333335, 2.786899518863159, 1.0989342374200721, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(33075, 'HP:0006705', 'Abnormal atrioventricular valve morphology', 'XPO:0129512', 'increased size of the cardiovascular system', 0.41304347826086957, 5.9590888072311134, 1.5688730886225806, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(33076, 'HP:0006705', 'Abnormal atrioventricular valve morphology', 'XPO:0102233', 'abnormal vascular endothelium morphology', 0.40425531914893614, 5.9590888072311134, 1.552093214856655, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(33077, 'HP:0004280', 'Irregular ossification of hand bones', 'XPO:0102484', 'abnormal interdigital region morphology', 0.4222222222222222, 6.173473740856008, 1.6144899509426371, 'UPHENO:0087006', 'abnormal autopod region morphology'),
(33078, 'HP:0004280', 'Irregular ossification of hand bones', 'XPO:0102054', 'abnormal notochord morphology', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(33079, 'HP:0004280', 'Irregular ossification of hand bones', 'XPO:0107372', 'abnormal flexural organ morphology', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(33080, 'HP:0004280', 'Irregular ossification of hand bones', 'XPO:0141723', 'abnormal posterior notochord morphology', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(33081, 'HP:0004280', 'Irregular ossification of hand bones', 'XPO:0102567', 'abnormal skeleton morphology', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(33082, 'HP:0004280', 'Irregular ossification of hand bones', 'XPO:0102806', 'abnormal articular system morphology', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(33083, 'HP:0004280', 'Irregular ossification of hand bones', 'XPO:0102217', 'abnormal elastica externa morphology', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(33084, 'HP:0004280', 'Irregular ossification of hand bones', 'XPO:0102097', 'abnormal skeletal system morphology', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(33085, 'HP:0004280', 'Irregular ossification of hand bones', 'XPO:0102272', 'abnormal notochordal sheath morphology', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(33086, 'HP:0004280', 'Irregular ossification of hand bones', 'XPO:0141719', 'abnormal anterior notochord morphology', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(33087, 'HP:0031221', 'Abnormal radioactive iodine uptake test result', 'XPO:0100225', 'abnormal endocrine system', 0.4482758620689655, 6.2194654996189955, 1.669741374719419, 'UPHENO:0003116', 'abnormal endocrine system'),
(33088, 'HP:0031221', 'Abnormal radioactive iodine uptake test result', 'XPO:0141629', 'metaplastic thyroid', 0.45714285714285713, 10.665155383737162, 2.208053351709177, 'UPHENO:0002689', 'abnormal thyroid gland'),
(33089, 'HP:0031221', 'Abnormal radioactive iodine uptake test result', 'XPO:0101023', 'abnormal ultimobranchial body', 0.40625, 6.2194654996189955, 1.5895464319170476, 'UPHENO:0003116', 'abnormal endocrine system'),
(33090, 'HP:0031221', 'Abnormal radioactive iodine uptake test result', 'XPO:0100840', 'abnormal thyroid', 0.45454545454545453, 10.665155383737162, 2.201771537126118, 'UPHENO:0002689', 'abnormal thyroid gland'),
(33091, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0125013', 'absent early embryonic cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(33092, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0101472', 'abnormal zygote cortex', 0.5652173913043478, 3.6715585125471644, 1.440565418328227, 'UPHENO:0086172', 'abnormal cell'),
(33093, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100610', 'abnormal appendage', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(33094, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100643', 'abnormal thoracic region', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(33095, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100332', 'abnormal germinal granule', 0.48148148148148145, 3.6715585125471644, 1.3295816755533123, 'UPHENO:0086172', 'abnormal cell'),
(33096, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0101518', 'abnormal B cell', 0.48148148148148145, 3.6715585125471644, 1.3295816755533123, 'UPHENO:0086172', 'abnormal cell'),
(33097, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0101327', 'abnormal blastomere V1.2.1', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(33098, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0139127', 'decreased cell population proliferation in joint region', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(33099, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0131145', 'abnormally increased number of polar body', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(33100, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0101023', 'abnormal ultimobranchial body', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(33101, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100784', 'abnormal left blastomere', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(33102, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0102526', 'abnormal nucleus morphology', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(33103, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0139622', 'decreased cell population proliferation in dorsal region', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(33104, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0130964', 'abnormally increased number of cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(33105, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0125530', 'absent chondroblast', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(33106, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0138233', 'decreased cell population proliferation in hindlimb region', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(33107, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0101333', 'abnormal barrier epithelial cell', 0.6190476190476191, 3.6715585125471644, 1.5076039119696991, 'UPHENO:0086172', 'abnormal cell'),
(33108, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100344', 'abnormal portion of organism substance', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(33109, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0138581', 'decreased cell population proliferation in male organism', 0.4166666666666667, 5.835653092541957, 1.5593338712067029, 'HP:0011017', 'Abnormal cellular physiology'),
(33110, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0138580', 'decreased cell population proliferation in female organism', 0.4166666666666667, 5.835653092541957, 1.5593338712067029, 'HP:0011017', 'Abnormal cellular physiology'),
(33111, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0101569', 'abnormal activin-induced ectoderm', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(33112, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100282', 'abnormal pelvic girdle primordium', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(33113, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0102336', 'abnormal Merkel cell morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(33114, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0131687', 'abnormal astral microtubule', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(33115, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0138585', 'decreased cell population proliferation in organism subdivision', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(33116, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100823', 'abnormal blood', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(33117, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0103179', 'abnormal lampbrush chromosome morphology', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(33118, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100894', 'abnormal nucleus', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(33119, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0139626', 'decreased cell population proliferation in antero-ventral region', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(33120, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0102024', 'abnormal cilium morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(33121, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100861', 'abnormal blastomere D2.2.2', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(33122, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0107253', 'abnormal enteric nervous system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(33123, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0102531', 'abnormal secondary spermatogonium morphology', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(33124, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0101237', 'abnormal mucus secreting cell', 0.6190476190476191, 3.6715585125471644, 1.5076039119696991, 'UPHENO:0086172', 'abnormal cell'),
(33125, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100069', 'abnormal urinary system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(33126, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0139670', 'decreased cell population proliferation in dorso-lateral region', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(33127, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100520', 'abnormal blastomere D1.2', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(33128, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0102873', 'abnormal nucleate erythrocyte morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(33129, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0135479', 'increased cell population proliferation in male organism', 0.4166666666666667, 5.835653092541957, 1.5593338712067029, 'HP:0011017', 'Abnormal cellular physiology'),
(33130, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0101657', 'abnormal oocyte morphology', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(33131, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0126783', 'abnormally localised exocrine cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(33132, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0130986', 'abnormally increased number of germ cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(33133, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0125061', 'absent basal body', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(33134, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0135509', 'increased cell population proliferation in embryonic structure', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(33135, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0142057', 'abnormal desmosome', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(33136, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0103041', 'abnormal perivitelline space morphology', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(33137, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0135504', 'increased cell population proliferation in multi-tissue structure', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(33138, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0133438', 'abnormal cilium morphology in the ciliated non-epidermal cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(33139, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0138715', 'decreased cell population proliferation in anatomical cluster', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(33140, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100265', 'abnormal sensory epithelial cell', 0.52, 3.6715585125471644, 1.3817418089225373, 'UPHENO:0086172', 'abnormal cell'),
(33141, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0131551', 'abnormally localised actin cytoskeleton', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(33142, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0126454', 'abnormally localised stem cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(33143, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0131096', 'abnormally increased number of exocrine cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(33144, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0102165', 'abnormal melanoblast morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(33145, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0131090', 'abnormally increased number of oxygen accumulating cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(33146, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100232', 'abnormal lymphatic system', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(33147, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0101071', 'abnormal endoplasmic reticulum', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(33148, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100289', 'abnormal chondroblast', 0.6190476190476191, 3.6715585125471644, 1.5076039119696991, 'UPHENO:0086172', 'abnormal cell'),
(33149, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0139423', 'decreased cell population proliferation in multicellular anatomical structure', 0.4166666666666667, 5.835653092541957, 1.5593338712067029, 'HP:0011017', 'Abnormal cellular physiology'),
(33150, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0131654', 'abnormal neuron projection', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(33151, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0125785', 'absent mitotic spindle', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(33152, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0101450', 'abnormal myeloid cell', 0.5, 3.6715585125471644, 1.3549093166236559, 'UPHENO:0086172', 'abnormal cell'),
(33153, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0139621', 'decreased cell population proliferation in posterior region', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(33154, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100511', 'abnormal stylopod', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(33155, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0141892', 'abnormal inositol metabolic process', 0.44, 4.758907843651163, 1.447038165082909, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(33156, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100515', 'abnormal somatic stem cell', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(33157, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0115391', 'abnormally undifferentiated alimentary system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(33158, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100967', 'abnormal blastomere V2.1.2', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(33159, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0102356', 'abnormal kinetochore morphology', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(33160, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100872', 'abnormal neuroendocrine cell', 0.48148148148148145, 3.6715585125471644, 1.3295816755533123, 'UPHENO:0086172', 'abnormal cell'),
(33161, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100317', 'abnormal respiratory system', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(33162, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0138820', 'decreased cell population proliferation in anatomical line', 0.4411764705882353, 5.835653092541957, 1.6045413160604438, 'HP:0011017', 'Abnormal cellular physiology'),
(33163, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100274', 'abnormal sensory system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(33164, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100691', 'abnormal keratin accumulating cell', 0.6190476190476191, 3.6715585125471644, 1.5076039119696991, 'UPHENO:0086172', 'abnormal cell'),
(33165, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0136028', 'increased cell population proliferation in interdigital region', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(33166, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0107259', 'abnormal animal-vegetal axis', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(33167, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100791', 'abnormal multiciliated cell precursor', 0.6190476190476191, 3.6715585125471644, 1.5076039119696991, 'UPHENO:0086172', 'abnormal cell'),
(33168, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100549', 'abnormal mitotic cell', 0.6190476190476191, 3.6715585125471644, 1.5076039119696991, 'UPHENO:0086172', 'abnormal cell'),
(33169, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0141438', 'increased cell population proliferation in tadpole', 0.4166666666666667, 5.835653092541957, 1.5593338712067029, 'HP:0011017', 'Abnormal cellular physiology'),
(33170, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0135477', 'increased cell population proliferation in whole organism', 0.42857142857142855, 5.835653092541957, 1.5814531869511603, 'HP:0011017', 'Abnormal cellular physiology'),
(33171, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0102306', 'abnormal secondary oogonium morphology', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(33172, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0101940', 'abnormal early embryonic cell morphology', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(33173, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0101658', 'abnormal germ cell morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(33174, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0131066', 'abnormally increased number of myoblast', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(33175, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0101072', 'abnormal mitochondrial cloud', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(33176, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0127513', 'abnormally localised nucleate erythrocyte', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(33177, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0126495', 'abnormally localised keratin accumulating cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(33178, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100104', 'abnormal embryonic structure', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(33179, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0115512', 'abnormally semi-erect whole organism', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(33180, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0138577', 'decreased cell population proliferation in anatomical group', 0.4166666666666667, 5.835653092541957, 1.5593338712067029, 'HP:0011017', 'Abnormal cellular physiology'),
(33181, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0130989', 'abnormally increased number of ciliated cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(33182, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100762', 'abnormal intersomitic region', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(33183, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100724', 'abnormal kinetochore', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(33184, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0141860', 'abnormal malate-aspartate shuttle', 0.4583333333333333, 4.758907843651163, 1.4768771428276568, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(33185, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0101513', 'abnormal basal body', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(33186, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0141767', 'abnormal temperature homeostasis', 0.4074074074074074, 4.758907843651163, 1.392413123563799, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(33187, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0138609', 'decreased cell population proliferation in tissue', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(33188, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0138606', 'decreased cell population proliferation in multi-tissue structure', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(33189, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100189', 'abnormal enteroendocrine cell', 0.48148148148148145, 3.6715585125471644, 1.3295816755533123, 'UPHENO:0086172', 'abnormal cell'),
(33190, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0107285', 'abnormal flexural organ', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(33191, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0127428', 'abnormally localised endoplasmic reticulum', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(33192, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0101325', 'abnormal blastomere D2.1.1', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(33193, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0101009', 'abnormal blastomere D1.1.1', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(33194, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0138584', 'decreased cell population proliferation in cell', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(33195, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0107273', 'abnormal basal region', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(33196, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0102520', 'abnormal microtubule morphology', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(33197, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0131666', 'abnormal adherens junction', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(33198, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100339', 'abnormal circumblastoporal collar', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(33199, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0131694', 'abnormal RNA polymerase II activity', 0.4230769230769231, 4.758907843651163, 1.418937661667548, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(33200, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0102061', 'abnormal spermatid morphology', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(33201, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0136520', 'increased cell population proliferation in dorsal region', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(33202, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0135160', 'increased cell population proliferation in embryo', 0.4166666666666667, 5.835653092541957, 1.5593338712067029, 'HP:0011017', 'Abnormal cellular physiology'),
(33203, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0141778', 'abnormal biosynthetic process', 0.4782608695652174, 4.758907843651163, 1.508641575552437, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(33204, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100665', 'abnormal egg jelly', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(33205, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100384', 'abnormal amputated tissue', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(33206, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0127171', 'abnormally localised myelin accumulating cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(33207, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0142051', 'abnormal cerebrospinal fluid', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(33208, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0131032', 'abnormally increased number of acid secreting cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(33209, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100573', 'abnormal extraembryonic structure', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(33210, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100203', 'abnormal endocrine cell', 0.5, 3.6715585125471644, 1.3549093166236559, 'UPHENO:0086172', 'abnormal cell'),
(33211, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0138576', 'decreased cell population proliferation in anatomical structure', 0.4411764705882353, 5.835653092541957, 1.6045413160604438, 'HP:0011017', 'Abnormal cellular physiology'),
(33212, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0136517', 'increased cell population proliferation in basal region', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(33213, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0127363', 'abnormally localised barrier cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(33214, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0135736', 'increased cell population proliferation in cell condensation', 0.4166666666666667, 5.835653092541957, 1.5593338712067029, 'HP:0011017', 'Abnormal cellular physiology'),
(33215, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0131247', 'abnormally decreased number of nucleate erythrocyte', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(33216, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0141276', 'decreased surface breathing', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(33217, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0131204', 'abnormally decreased number of pericyte', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(33218, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0101311', 'abnormal bottle cell', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(33219, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0127029', 'abnormally localised multiciliated cell precursor', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(33220, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0127876', 'abnormally localised microtubule', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(33221, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100295', 'abnormal extracellular matrix', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(33222, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0131389', 'abnormally decreased number of barrier epithelial cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(33223, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100688', 'abnormal adipose tissue', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(33224, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0131354', 'abnormally decreased number of multiciliated cell precursor', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(33225, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0142065', 'abnormally decreased number of desmosome', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(33226, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100152', 'abnormal alimentary system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(33227, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0125854', 'absent barrier epithelial cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(33228, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0141289', 'abnormal spindle microtubule morphology', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(33229, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0136191', 'increased cell population proliferation in organ part', 0.42857142857142855, 5.835653092541957, 1.5814531869511603, 'HP:0011017', 'Abnormal cellular physiology'),
(33230, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0127631', 'abnormally localised centriole', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(33231, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0131202', 'abnormally decreased number of germ cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(33232, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0107339', 'abnormal yolk platelet', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(33233, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100581', 'abnormal immune system', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(33234, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100882', 'abnormal perichondrial cell', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(33235, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0127824', 'abnormally localised alkali secreting cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(33236, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100202', 'abnormal embryo', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(33237, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0125997', 'absent Merkel cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(33238, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100397', 'abnormal ventral vegetal hemisphere blastomere', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(33239, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0115505', 'dead whole organism', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(33240, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100251', 'abnormal proteinaceous extracellular matrix', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(33241, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0131348', 'abnormally decreased number of absorptive cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(33242, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100481', 'abnormal anatomical line', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(33243, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0126318', 'abnormally localised cell', 0.48148148148148145, 3.6715585125471644, 1.3295816755533123, 'UPHENO:0086172', 'abnormal cell'),
(33244, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100902', 'abnormal spermatocyte', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(33245, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0101220', 'abnormal centriole', 0.5652173913043478, 3.6715585125471644, 1.440565418328227, 'UPHENO:0086172', 'abnormal cell'),
(33246, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100273', 'abnormal visual system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(33247, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100035', 'abnormal ventral animal hemisphere blastomere', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(33248, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100386', 'abnormal limb', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(33249, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0131165', 'abnormally increased number of cementoblast', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(33250, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0125160', 'absent exocrine cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(33251, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100277', 'abnormal blastocoel', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(33252, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100415', 'abnormal secretory epithelial cell', 0.52, 3.6715585125471644, 1.3817418089225373, 'UPHENO:0086172', 'abnormal cell'),
(33253, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100544', 'abnormal neuromast support cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(33254, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0141738', 'abnormal carbon dioxide homeostasis', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(33255, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100551', 'abnormal oocyte cortex', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(33256, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0101176', 'abnormal non-ciliated epithelial cell', 0.52, 3.6715585125471644, 1.3817418089225373, 'UPHENO:0086172', 'abnormal cell'),
(33257, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0126413', 'abnormally localised cell part', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(33258, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0126738', 'abnormally localised paracrine cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(33259, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0127533', 'abnormally localised spermatocyte', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(33260, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0141296', 'abnormal adherens junction morphology', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(33261, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0126162', 'absent alkali secreting cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(33262, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100976', 'abnormal multiciliated cell', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(33263, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0141797', 'abnormal hydrogen metabolic process', 0.4782608695652174, 4.758907843651163, 1.508641575552437, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(33264, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0141790', 'abnormal cellular metabolic process', 0.4583333333333333, 4.758907843651163, 1.4768771428276568, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(33265, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0136516', 'increased cell population proliferation in axial region', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(33266, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100915', 'abnormal dermal system', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(33267, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0101168', 'abnormal circulating cell', 0.52, 3.6715585125471644, 1.3817418089225373, 'UPHENO:0086172', 'abnormal cell'),
(33268, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0101192', 'abnormal blastomere D2.1', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(33269, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0125698', 'absent filopodium', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(33270, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0107311', 'abnormal apical junction complex', 0.5, 3.6715585125471644, 1.3549093166236559, 'UPHENO:0086172', 'abnormal cell'),
(33271, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0102965', 'abnormal barrier epithelial cell morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(33272, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0107426', 'abnormal yolk platelet morphology', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(33273, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0102347', 'abnormal ciliated cell morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(33274, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0138262', 'decreased cell population proliferation in embryo', 0.4166666666666667, 5.835653092541957, 1.5593338712067029, 'HP:0011017', 'Abnormal cellular physiology'),
(33275, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100569', 'abnormal motor axon', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(33276, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0103642', 'increased cell population proliferation', 0.5172413793103449, 5.835653092541957, 1.7373661832679608, 'HP:0011017', 'Abnormal cellular physiology'),
(33277, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0115615', 'abnormally posteriorly mislocalised primordial germ cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(33278, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0101096', 'abnormal tendon', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(33279, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0101157', 'abnormal female organism', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(33280, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0131523', 'absent actin filament', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(33281, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100192', 'abnormal epithelium', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(33282, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0101264', 'abnormal mitotic spindle', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(33283, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0101587', 'abnormal hemangioblast', 0.5, 3.6715585125471644, 1.3549093166236559, 'UPHENO:0086172', 'abnormal cell'),
(33284, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0101500', 'abnormal endodermal cell', 0.48148148148148145, 3.6715585125471644, 1.3295816755533123, 'UPHENO:0086172', 'abnormal cell'),
(33285, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100965', 'abnormal blastomere V2.2', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(33286, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0124934', 'absent centrosome', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(33287, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0107261', 'abnormal dorsal-ventral axis', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(33288, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0138578', 'decreased cell population proliferation in anatomical system', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(33289, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0141266', 'abnormal surface breathing', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(33290, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0138424', 'decreased cell population proliferation in marginal zone (sensu neural)', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(33291, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0127819', 'abnormally localised ciliary axoneme', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(33292, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0142067', 'abnormally necrotic desmosome', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(33293, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0124884', 'absent keratin accumulating cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(33294, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0101969', 'abnormal zygote morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(33295, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0135718', 'increased cell population proliferation in anatomical line', 0.4411764705882353, 5.835653092541957, 1.6045413160604438, 'HP:0011017', 'Abnormal cellular physiology'),
(33296, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0103099', 'abnormal alkali secreting cell morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(33297, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100216', 'abnormal hepato-pancreatic progenitor cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(33298, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0102860', 'abnormal mesenchymal stem cell morphology', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(33299, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100337', 'abnormal zygote', 0.6190476190476191, 3.6715585125471644, 1.5076039119696991, 'UPHENO:0086172', 'abnormal cell'),
(33300, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100392', 'abnormal cilium', 0.5652173913043478, 3.6715585125471644, 1.440565418328227, 'UPHENO:0086172', 'abnormal cell'),
(33301, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0131706', 'abnormal ciliary basal body organization', 0.5555555555555556, 5.835653092541957, 1.8005636605953823, 'HP:0011017', 'Abnormal cellular physiology'),
(33302, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0107260', 'abnormal anterior-posterior axis', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(33303, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0101467', 'abnormal alkali secreting cell', 0.6190476190476191, 3.6715585125471644, 1.5076039119696991, 'UPHENO:0086172', 'abnormal cell'),
(33304, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0135131', 'increased cell population proliferation in hindlimb region', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(33305, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100070', 'abnormal anatomical system', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(33306, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0142064', 'abnormal desmosome morphology', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(33307, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100449', 'abnormal lymphocyte', 0.5, 3.6715585125471644, 1.3549093166236559, 'UPHENO:0086172', 'abnormal cell'),
(33308, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0141743', 'abnormal chemical homeostasis within a tissue', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(33309, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0138738', 'decreased cell population proliferation in anatomical region', 0.4166666666666667, 5.835653092541957, 1.5593338712067029, 'HP:0011017', 'Abnormal cellular physiology'),
(33310, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0107258', 'abnormal anatomical axis', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(33311, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0126548', 'abnormally localised centrosome', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(33312, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0136526', 'increased cell population proliferation in postero-ventral region', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(33313, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0101120', 'abnormal cardiac progenitor cell', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(33314, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0131031', 'abnormally increased number of nucleate erythrocyte', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(33315, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0139618', 'decreased cell population proliferation in axial region', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(33316, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0131328', 'abnormally decreased number of paracrine cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(33317, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0101547', 'abnormal lampbrush chromosome', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(33318, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0107267', 'abnormal ventral side', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(33319, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100062', 'abnormal anatomical space', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(33320, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0101921', 'abnormal chondroblast morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(33321, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100402', 'abnormal zeugopod', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(33322, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100335', 'abnormal commissural interneuron', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(33323, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0127806', 'abnormally localised spermatid', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(33324, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0141796', 'abnormal demethylation', 0.4782608695652174, 4.758907843651163, 1.508641575552437, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(33325, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0127217', 'abnormally localised cilium', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(33326, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0136525', 'increased cell population proliferation in postero-dorsal region', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(33327, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100422', 'abnormal notochord', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(33328, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0101411', 'abnormal marginal zone (sensu neural)', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(33329, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0141421', 'decreased cell population proliferation in tadpole', 0.4166666666666667, 5.835653092541957, 1.5593338712067029, 'HP:0011017', 'Abnormal cellular physiology'),
(33330, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100533', 'abnormal melanoblast', 0.6190476190476191, 3.6715585125471644, 1.5076039119696991, 'UPHENO:0086172', 'abnormal cell'),
(33331, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0101302', 'abnormal subcortical cytoplasm', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(33332, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0133443', 'abnormally increased number of cilium in the multiciliated cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(33333, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0101514', 'abnormal dendrite', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(33334, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100596', 'abnormal myocyte', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(33335, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0115508', 'abnormally peramorphic growth of whole organism', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(33336, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100913', 'abnormal Brachets cleft', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(33337, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0101198', 'abnormal digestive enzyme secreting cell', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(33338, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0101158', 'abnormal blastomere V2.2.2', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(33339, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0102934', 'abnormal subcortical cytoplasm morphology', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(33340, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0131531', 'absent cortical actin cytoskeleton', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(33341, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100667', 'abnormal vegetal yolk mass', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(33342, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0127160', 'abnormally localised acid secreting cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(33343, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100316', 'abnormal gamete', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(33344, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100888', 'abnormal microtubule', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(33345, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100176', 'abnormal stage VI oocyte', 0.5652173913043478, 3.6715585125471644, 1.440565418328227, 'UPHENO:0086172', 'abnormal cell'),
(33346, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0101515', 'abnormal neuromast mantle cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(33347, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100728', 'abnormal cell condensation', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(33348, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0101174', 'abnormal articular system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(33349, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0126082', 'absent perivitelline space', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(33350, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0141498', 'abnormal axon microtubule bundle', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(33351, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100653', 'abnormal myoblast', 0.6190476190476191, 3.6715585125471644, 1.5076039119696991, 'UPHENO:0086172', 'abnormal cell'),
(33352, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0125868', 'absent cementoblast', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(33353, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0125693', 'absent mucus secreting cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(33354, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100175', 'abnormal migrating neuroblast', 0.5, 3.6715585125471644, 1.3549093166236559, 'UPHENO:0086172', 'abnormal cell'),
(33355, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0131278', 'abnormally decreased number of keratin accumulating cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(33356, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0127821', 'abnormally localised apoptotic cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(33357, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0141715', 'abnormal septum', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(33358, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100654', 'abnormal blastomere V2.1', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(33359, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0138818', 'decreased cell population proliferation in portion of organism substance', 0.4411764705882353, 5.835653092541957, 1.6045413160604438, 'HP:0011017', 'Abnormal cellular physiology'),
(33360, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0141267', 'abnormal resting posture', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(33361, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0101480', 'abnormal stage V oocyte', 0.5652173913043478, 3.6715585125471644, 1.440565418328227, 'UPHENO:0086172', 'abnormal cell'),
(33362, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100638', 'abnormal polar body', 0.6190476190476191, 3.6715585125471644, 1.5076039119696991, 'UPHENO:0086172', 'abnormal cell'),
(33363, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0101534', 'abnormal blastomere V2.1.1', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(33364, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100377', 'abnormal connective tissue', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(33365, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0133436', 'abnormal cilium morphology in the multiciliated cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(33366, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0125743', 'absent lampbrush chromosome', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(33367, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0101405', 'abnormal ring structure', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(33368, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100954', 'abnormal neural progenitor cell', 0.48148148148148145, 3.6715585125471644, 1.3295816755533123, 'UPHENO:0086172', 'abnormal cell'),
(33369, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0131725', 'abnormal phosphorylation of RNA polymerase II C-terminal domain', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(33370, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0101187', 'abnormal dorsolateral commissural neuron', 0.48148148148148145, 3.6715585125471644, 1.3295816755533123, 'UPHENO:0086172', 'abnormal cell'),
(33371, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0136025', 'increased cell population proliferation in joint region', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(33372, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0102608', 'abnormal multiciliated cell morphology', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(33373, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0127979', 'abnormally localised absorptive cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(33374, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0129551', 'increased size of the cell part', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(33375, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100164', 'abnormal neural nucleus', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(33376, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0101576', 'abnormal blastomere V1.2.2', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(33377, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0141784', 'abnormal cellular hormone metabolic process', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(33378, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0127643', 'abnormally localised somatic stem cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(33379, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0141783', 'abnormal collagen metabolic process', 0.4782608695652174, 4.758907843651163, 1.508641575552437, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(33380, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0125724', 'absent polar body', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(33381, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0131195', 'abnormally decreased number of Merkel cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(33382, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0107262', 'abnormal left-right axis', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(33383, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0101228', 'abnormal mesenchymal stem cell', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(33384, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0141898', 'abnormal maltose metabolic process', 0.4230769230769231, 4.758907843651163, 1.418937661667548, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(33385, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100114', 'abnormal peripheral nervous system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(33386, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100493', 'abnormal liver and biliary system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(33387, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0101452', 'abnormal blastomere V1.1.1', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(33388, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100205', 'abnormal limb segment', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(33389, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0136568', 'increased cell population proliferation in dorso-lateral region', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(33390, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100004', 'abnormal cell', 0.65, 3.6715585125471644, 1.5448343060521594, 'UPHENO:0086172', 'abnormal cell'),
(33391, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100416', 'abnormal ligament', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(33392, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0131707', 'abnormal cilium assembly', 0.5172413793103449, 5.835653092541957, 1.7373661832679608, 'HP:0011017', 'Abnormal cellular physiology'),
(33393, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100028', 'abnormal anatomical cluster', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(33394, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0131559', 'abnormally localised spindle microtubule', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(33395, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0101239', 'abnormal olfactory epithelial support cell', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(33396, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100009', 'abnormal multi-tissue structure', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(33397, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0139617', 'decreased cell population proliferation in apical region', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(33398, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0136522', 'increased cell population proliferation in medial region', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(33399, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100924', 'abnormal spermatozoon', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(33400, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100676', 'abnormal blastomere D2.2', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(33401, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100196', 'abnormal neuron', 0.5, 3.6715585125471644, 1.3549093166236559, 'UPHENO:0086172', 'abnormal cell'),
(33402, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0139628', 'decreased cell population proliferation in postero-ventral region', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(33403, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0130979', 'abnormally increased number of Merkel cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(33404, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0131129', 'abnormally increased number of chondroblast', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(33405, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100557', 'abnormal prime meridian', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(33406, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0101636', 'abnormal cell morphology', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(33407, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0141788', 'abnormal hormone biosynthetic process', 0.4074074074074074, 4.758907843651163, 1.392413123563799, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(33408, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100817', 'abnormal intersomitic neuron', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(33409, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0131346', 'abnormally decreased number of chondroblast', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(33410, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0102994', 'abnormal vegetal cortex morphology', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(33411, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0101297', 'abnormal barrier cell', 0.6190476190476191, 3.6715585125471644, 1.5076039119696991, 'UPHENO:0086172', 'abnormal cell'),
(33412, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0101374', 'abnormal migratory neural crest cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(33413, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0131569', 'abnormally localised cortical actin cytoskeleton', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(33414, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0127794', 'abnormally localised mitotic cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(33415, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100010', 'abnormal multicellular anatomical structure', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(33416, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0127975', 'abnormally localised mitochondrial cloud', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(33417, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0101406', 'abnormal cleavage furrow', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(33418, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0125394', 'absent multiciliated cell precursor', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(33419, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0141772', 'abnormal water homeostasis', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(33420, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0131307', 'abnormally decreased number of mitotic cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(33421, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0125644', 'absent pericyte', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(33422, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0126314', 'absent absorptive cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(33423, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0107399', 'abnormal filopodium morphology', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(33424, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0101037', 'abnormal hatching gland cell', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(33425, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0141841', 'abnormality of whole organism mass', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(33426, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0102181', 'abnormal mitotic cell morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(33427, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0102636', 'abnormal acid secreting cell morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(33428, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0141795', 'abnormal glycosylation', 0.44, 4.758907843651163, 1.447038165082909, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(33429, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100742', 'abnormal musculoskeletal system', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(33430, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100151', 'abnormal primordium', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(33431, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100956', 'abnormal centrosome', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(33432, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0136515', 'increased cell population proliferation in apical region', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(33433, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0124845', 'absent stem cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(33434, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0138717', 'decreased cell population proliferation in acellular anatomical structure', 0.4166666666666667, 5.835653092541957, 1.5593338712067029, 'HP:0011017', 'Abnormal cellular physiology'),
(33435, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0101200', 'abnormal joint region', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(33436, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0116091', 'abnormally increased variability of size of cell in endoderm', 0.48148148148148145, 3.6715585125471644, 1.3295816755533123, 'UPHENO:0086172', 'abnormal cell'),
(33437, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100307', 'abnormal blastomere', 0.5652173913043478, 3.6715585125471644, 1.440565418328227, 'UPHENO:0086172', 'abnormal cell'),
(33438, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0141511', 'abnormally localised nucleus in myoblast', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(33439, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0130988', 'abnormally increased number of pericyte', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(33440, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0102896', 'abnormal mitotic spindle morphology', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(33441, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100014', 'abnormal tissue', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(33442, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0101448', 'abnormal myelin accumulating cell', 0.6190476190476191, 3.6715585125471644, 1.5076039119696991, 'UPHENO:0086172', 'abnormal cell'),
(33443, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0141745', 'abnormal creatinine homeostasis', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(33444, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0102534', 'abnormal spermatocyte morphology', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(33445, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0126671', 'abnormally localised zygote', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(33446, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100547', 'abnormal blastomere V2', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(33447, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0141791', 'abnormal primary metabolic process', 0.4782608695652174, 4.758907843651163, 1.508641575552437, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(33448, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0103414', 'abnormally increased number of vacuole in the spermatozoon', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(33449, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0142066', 'abnormally increased number of desmosome', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(33450, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0141776', 'abnormal metabolic process', 0.5238095238095238, 4.758907843651163, 1.5788480773767701, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(33451, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100587', 'abnormal vestibuloauditory system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(33452, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0131708', 'abnormal cilium disassembly', 0.5555555555555556, 5.835653092541957, 1.8005636605953823, 'HP:0011017', 'Abnormal cellular physiology'),
(33453, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0102703', 'abnormal endoplasmic reticulum morphology', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(33454, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0126473', 'abnormally localised germ cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(33455, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0102852', 'abnormal centriole morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(33456, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0107271', 'abnormal apical region', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(33457, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0135482', 'increased cell population proliferation in cell', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(33458, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100649', 'abnormal growth cone', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(33459, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0126628', 'abnormally localised blastomere', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(33460, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100640', 'abnormal notochordal sheath', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(33461, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0124807', 'absent cell part', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(33462, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100268', 'abnormal circulatory system', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(33463, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0101022', 'abnormal blastomere V1.2', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(33464, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0107276', 'abnormal dorsal region', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(33465, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0133473', 'abnormally decreased number of cilium in the ciliated non-epidermal cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(33466, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0135483', 'increased cell population proliferation in organism subdivision', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(33467, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0125053', 'absent zygote', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(33468, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100781', 'abnormal presumptive ectoderm', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(33469, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0107286', 'abnormal efferent neuron', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(33470, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0101109', 'abnormal egg cell-free extract', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(33471, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100135', 'abnormal surface structure', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(33472, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0131110', 'abnormally increased number of paracrine cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(33473, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0103021', 'abnormal wedge region morphology', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(33474, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100258', 'abnormal organ part', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(33475, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0101504', 'abnormal blastomere D2.2.1', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(33476, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100842', 'abnormal left-dorsal blastomere', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(33477, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0107270', 'abnormal proximal-distal axis', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(33478, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0131561', 'abnormally localised actin filament', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(33479, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100856', 'abnormal simple organ', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(33480, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100429', 'abnormal spermatid', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(33481, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0101535', 'abnormal absorptive cell', 0.6190476190476191, 3.6715585125471644, 1.5076039119696991, 'UPHENO:0086172', 'abnormal cell'),
(33482, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0136398', 'increased cell population proliferation in egg jelly', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(33483, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0131667', 'abnormal actin cytoskeleton', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(33484, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100585', 'abnormal elastica externa', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(33485, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0101494', 'abnormal blastomere D1.2.1', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(33486, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100032', 'abnormal nervous system', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(33487, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0131189', 'abnormally decreased number of stem cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(33488, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100395', 'abnormal blastomere D1.1', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(33489, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100423', 'abnormal process', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(33490, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0138822', 'decreased cell population proliferation in extraembryonic structure', 0.4166666666666667, 5.835653092541957, 1.5593338712067029, 'HP:0011017', 'Abnormal cellular physiology'),
(33491, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0139625', 'decreased cell population proliferation in antero-dorsal region', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(33492, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0101389', 'abnormal wedge region', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(33493, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0124864', 'absent germ cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(33494, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0124984', 'absent progenitor cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(33495, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0139620', 'decreased cell population proliferation in anterior region', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(33496, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0138232', 'decreased cell population proliferation in forelimb region', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(33497, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0103145', 'abnormal basal body morphology', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(33498, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0138611', 'decreased cell population proliferation in embryonic structure', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(33499, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0101497', 'abnormal ciliary axoneme', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(33500, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100023', 'abnormal mesenchyme', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(33501, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100336', 'abnormal interneuron', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(33502, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0141714', 'abnormal anterior notochord', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(33503, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0141789', 'abnormal hormone catabolic process', 0.4074074074074074, 4.758907843651163, 1.392413123563799, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(33504, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0102929', 'abnormal barrier cell morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(33505, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100239', 'abnormal acellular anatomical structure', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(33506, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0141792', 'abnormal small molecule metabolic process', 0.4782608695652174, 4.758907843651163, 1.508641575552437, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(33507, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0142052', 'abnormal nasal region', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(33508, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100363', 'abnormal cardiovascular system', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(33509, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100465', 'abnormal skeletal system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(33510, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0107371', 'abnormal migrating myoblast morphology', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(33511, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0127372', 'abnormally localised polar body', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(33512, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0101358', 'abnormal endothelial cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(33513, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0135613', 'increased cell population proliferation in anatomical cluster', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(33514, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0141748', 'abnormal gas homeostasis', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(33515, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0101004', 'abnormal acid secreting cell', 0.6190476190476191, 3.6715585125471644, 1.5076039119696991, 'UPHENO:0086172', 'abnormal cell'),
(33516, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0127338', 'abnormally localised mucus secreting cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(33517, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0131153', 'abnormally increased number of electrically active cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(33518, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100293', 'abnormal duct', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(33519, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100084', 'abnormal anatomical group', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(33520, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0101132', 'abnormal apoptotic cell', 0.6190476190476191, 3.6715585125471644, 1.5076039119696991, 'UPHENO:0086172', 'abnormal cell'),
(33521, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100570', 'abnormal axon', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(33522, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0139500', 'decreased cell population proliferation in egg jelly', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(33523, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0127896', 'abnormally localised ring structure', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(33524, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100912', 'abnormal trabecula', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(33525, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0135474', 'increased cell population proliferation in anatomical structure', 0.4411764705882353, 5.835653092541957, 1.6045413160604438, 'HP:0011017', 'Abnormal cellular physiology'),
(33526, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0136524', 'increased cell population proliferation in antero-ventral region', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(33527, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0116494', 'absent biological process', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(33528, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100501', 'abnormal urogenital system', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(33529, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0101575', 'abnormal vitelline membrane', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(33530, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100477', 'abnormal pericyte', 0.6190476190476191, 3.6715585125471644, 1.5076039119696991, 'UPHENO:0086172', 'abnormal cell'),
(33531, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0107325', 'abnormal adult thrombocyte', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(33532, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0141771', 'abnormal urea homeostasis', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(33533, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0141798', 'abnormal lipid metabolic process', 0.44, 4.758907843651163, 1.447038165082909, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(33534, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0131300', 'abnormally decreased number of alkali secreting cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(33535, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0126214', 'absent microtubule', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(33536, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0142056', 'abnormal main body axis', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(33537, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100745', 'abnormal anterior lymph sac', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(33538, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100521', 'abnormal animal blastomere', 0.48148148148148145, 3.6715585125471644, 1.3295816755533123, 'UPHENO:0086172', 'abnormal cell'),
(33539, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0101740', 'abnormal cell part morphology', 0.48148148148148145, 3.6715585125471644, 1.3295816755533123, 'UPHENO:0086172', 'abnormal cell'),
(33540, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0101345', 'abnormal ascending interneuron', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(33541, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0127339', 'abnormally localised migrating myoblast', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(33542, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100599', 'abnormal adult immune system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(33543, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100031', 'abnormal central nervous system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(33544, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0102704', 'abnormal mitochondrial cloud morphology', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(33545, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0131089', 'abnormally increased number of mitotic cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(33546, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0127343', 'abnormally localised filopodium', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(33547, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0116434', 'abnormal biological process', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(33548, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0136523', 'increased cell population proliferation in antero-dorsal region', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(33549, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0101133', 'abnormal motor neuron', 0.48148148148148145, 3.6715585125471644, 1.3295816755533123, 'UPHENO:0086172', 'abnormal cell'),
(33550, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0101078', 'abnormal mucous gland', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(33551, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0131297', 'abnormally decreased number of melanoblast', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(33552, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0102693', 'abnormal plasma membrane morphology', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(33553, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0103093', 'abnormal sperm entry point morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(33554, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100546', 'abnormal whole organism', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(33555, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0102353', 'abnormal centromere morphology', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(33556, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0126388', 'abnormally localised oocyte', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(33557, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0126472', 'abnormally localised secondary spermatogonium', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(33558, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100458', 'abnormal autopod', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(33559, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0125976', 'absent centriole', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(33560, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0125454', 'absent myoblast', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(33561, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0102147', 'abnormal somatic stem cell morphology', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(33562, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0131130', 'abnormally increased number of myelin accumulating cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(33563, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0101804', 'abnormal stem cell morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(33564, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0131136', 'abnormally increased number of multiciliated cell precursor', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(33565, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0101326', 'abnormal cementoblast', 0.6190476190476191, 3.6715585125471644, 1.5076039119696991, 'UPHENO:0086172', 'abnormal cell'),
(33566, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0130968', 'abnormally increased number of early embryonic cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(33567, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0127508', 'abnormally localised barrier epithelial cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(33568, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100509', 'abnormal germ plasm', 0.5, 3.6715585125471644, 1.3549093166236559, 'UPHENO:0086172', 'abnormal cell'),
(33569, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0131513', 'absent actin cytoskeleton', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(33570, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0141264', 'abnormal schooling behavior', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(33571, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0101519', 'abnormal hypobranchial placode', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(33572, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0102872', 'abnormal ciliated non-epidermal cell morphology', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(33573, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0101278', 'abnormal pigment cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(33574, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0126725', 'abnormally localised epithelial cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(33575, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0101079', 'abnormal blastomere D1.1.2', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(33576, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0103104', 'abnormal zygote cortex morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(33577, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100120', 'abnormal genital system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(33578, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100852', 'abnormal interdigital region', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(33579, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0107323', 'abnormal thrombocyte', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(33580, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0141904', 'abnormal glucosamine metabolic process', 0.4782608695652174, 4.758907843651163, 1.508641575552437, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(33581, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0101373', 'abnormal oxygen accumulating cell', 0.6190476190476191, 3.6715585125471644, 1.5076039119696991, 'UPHENO:0086172', 'abnormal cell'),
(33582, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0131512', 'absent adherens junction', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(33583, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0101481', 'abnormal skeletal muscle satellite cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(33584, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100034', 'abnormal blastomere V1.1', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(33585, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0102183', 'abnormal oocyte cortex morphology', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(33586, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0103631', 'abnormally increased number of apoptotic cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(33587, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0135735', 'increased cell population proliferation in process', 0.4166666666666667, 5.835653092541957, 1.5593338712067029, 'HP:0011017', 'Abnormal cellular physiology'),
(33588, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0127476', 'abnormally localised nucleus', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(33589, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100989', 'abnormal right blastomere', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(33590, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0130973', 'abnormally increased number of stem cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(33591, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0135130', 'increased cell population proliferation in forelimb region', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(33592, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0101141', 'abnormal Keller explant', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(33593, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0141499', 'abnormal tadpole', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(33594, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0102768', 'abnormal ooplasm morphology', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(33595, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100732', 'abnormal tendon fibroblast', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(33596, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0131314', 'abnormally decreased number of exocrine cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(33597, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0131134', 'abnormally increased number of barrier cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(33598, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100396', 'abnormal dorsal animal hemisphere blastomere', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(33599, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0141315', 'abnormal anatomical region', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(33600, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100372', 'abnormal hematological system', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(33601, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0102539', 'abnormal cytoplasm morphology', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(33602, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0107272', 'abnormal axial region', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(33603, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0141271', 'increased surface breathing', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(33604, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100807', 'abnormal matrix-based tissue', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(33605, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0101451', 'abnormal dorsal lymph space', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(33606, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0131675', 'abnormal spindle microtubule', 0.5652173913043478, 3.6715585125471644, 1.440565418328227, 'UPHENO:0086172', 'abnormal cell'),
(33607, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0107266', 'abnormal dorsal side', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(33608, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100969', 'abnormal disaggregated/reaggregated ectoderm treated with activin', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(33609, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0127168', 'abnormally localised chondroblast', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(33610, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0138890', 'decreased cell population proliferation in intersomitic region', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(33611, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0101241', 'abnormal nucleate erythrocyte', 0.6190476190476191, 3.6715585125471644, 1.5076039119696991, 'UPHENO:0086172', 'abnormal cell'),
(33612, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0125859', 'absent nucleate erythrocyte', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(33613, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0101485', 'abnormal descending interneuron', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(33614, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100231', 'abnormal compound organ', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(33615, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0131171', 'abnormally increased number of barrier epithelial cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(33616, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100754', 'abnormal electrically active cell', 0.6190476190476191, 3.6715585125471644, 1.5076039119696991, 'UPHENO:0086172', 'abnormal cell'),
(33617, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0133471', 'abnormally decreased number of cilium in the ciliated cell', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(33618, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0102764', 'abnormal apoptotic cell morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(33619, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0127815', 'abnormally localised ciliated non-epidermal cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(33620, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0139293', 'decreased cell population proliferation in organ part', 0.42857142857142855, 5.835653092541957, 1.5814531869511603, 'HP:0011017', 'Abnormal cellular physiology'),
(33621, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100733', 'abnormal fibroblast', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(33622, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0101162', 'abnormal stromal cell', 0.48148148148148145, 3.6715585125471644, 1.3295816755533123, 'UPHENO:0086172', 'abnormal cell'),
(33623, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0107284', 'abnormal migrating myoblast', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(33624, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0141775', 'abnormal nitrogen compound metabolic process', 0.4782608695652174, 4.758907843651163, 1.508641575552437, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(33625, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0141787', 'abnormal hormone metabolic process', 0.4782608695652174, 4.758907843651163, 1.508641575552437, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(33626, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100006', 'abnormal anatomical structure', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(33627, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0127288', 'abnormally localised pericyte', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(33628, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100993', 'abnormal ligament cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(33629, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0139580', 'decreased cell population proliferation in thoracic region', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(33630, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0135636', 'increased cell population proliferation in anatomical region', 0.4166666666666667, 5.835653092541957, 1.5593338712067029, 'HP:0011017', 'Abnormal cellular physiology'),
(33631, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100025', 'abnormal oocyte', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(33632, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0127743', 'abnormally localised perivitelline space', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(33633, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0101040', 'abnormal axial mesoderm', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(33634, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0141285', 'abnormal cortical actin cytoskeleton morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(33635, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0131685', 'abnormal cortical actin cytoskeleton', 0.5652173913043478, 3.6715585125471644, 1.440565418328227, 'UPHENO:0086172', 'abnormal cell'),
(33636, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0141314', 'abnormal Roux spot morphology', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(33637, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0135476', 'increased cell population proliferation in anatomical system', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(33638, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0127391', 'abnormally localised lampbrush chromosome', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(33639, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100285', 'abnormal progenitor cell', 0.6190476190476191, 3.6715585125471644, 1.5076039119696991, 'UPHENO:0086172', 'abnormal cell'),
(33640, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100081', 'abnormal anatomical entity in vitro', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(33641, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0131180', 'abnormally decreased number of cell', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(33642, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0103080', 'abnormal myelin accumulating cell morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(33643, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100674', 'abnormal secondary oogonium', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(33644, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0101366', 'abnormal morula cell', 0.5652173913043478, 3.6715585125471644, 1.440565418328227, 'UPHENO:0086172', 'abnormal cell'),
(33645, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0127520', 'abnormally localised gastrula cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(33646, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0141770', 'abnormal urate homeostasis', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(33647, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0101498', 'abnormal stage II oocyte', 0.5652173913043478, 3.6715585125471644, 1.440565418328227, 'UPHENO:0086172', 'abnormal cell'),
(33648, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0141497', 'abnormal lymphoblast', 0.5, 3.6715585125471644, 1.3549093166236559, 'UPHENO:0086172', 'abnormal cell'),
(33649, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0101378', 'abnormal blastomere D1', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(33650, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0101136', 'abnormal ooplasm', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(33651, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0107269', 'abnormal right side', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(33652, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0135720', 'increased cell population proliferation in extraembryonic structure', 0.4166666666666667, 5.835653092541957, 1.5593338712067029, 'HP:0011017', 'Abnormal cellular physiology'),
(33653, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0141277', 'abnormal actin cytoskeleton morphology', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(33654, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0101283', 'abnormal left-ventral blastomere', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(33655, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0139627', 'decreased cell population proliferation in postero-dorsal region', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(33656, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100394', 'abnormal marginal zone', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(33657, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100702', 'abnormal glial cell', 0.5, 3.6715585125471644, 1.3549093166236559, 'UPHENO:0086172', 'abnormal cell'),
(33658, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0107288', 'abnormal larval alimentary system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(33659, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0101466', 'abnormal secondary myofiber', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(33660, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0107264', 'abnormal anterior side', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(33661, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0131131', 'abnormally increased number of absorptive cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(33662, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0101107', 'abnormal erythroid cell', 0.5, 3.6715585125471644, 1.3549093166236559, 'UPHENO:0086172', 'abnormal cell'),
(33663, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0136518', 'increased cell population proliferation in anterior region', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(33664, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0103894', 'abnormally decreased number of spindle microtubule', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(33665, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0125533', 'absent myelin accumulating cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(33666, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0107324', 'abnormal embryonic thrombocyte', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(33667, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0101083', 'abnormal T cell', 0.48148148148148145, 3.6715585125471644, 1.3295816755533123, 'UPHENO:0086172', 'abnormal cell'),
(33668, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0102258', 'abnormal primordial germ cell morphology', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(33669, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0127703', 'abnormally localised morula cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(33670, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100715', 'abnormal ciliated cell', 0.6190476190476191, 3.6715585125471644, 1.5076039119696991, 'UPHENO:0086172', 'abnormal cell'),
(33671, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0131075', 'abnormally increased number of mucus secreting cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(33672, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0102869', 'abnormal mucus secreting cell morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(33673, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0131383', 'abnormally decreased number of cementoblast', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(33674, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0125692', 'absent oxygen accumulating cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(33675, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100427', 'abnormal olfactory system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(33676, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0102423', 'abnormal multiciliated cell precursor morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(33677, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0136567', 'increased cell population proliferation in ventro-lateral region', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(33678, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0101463', 'abnormal right-ventral blastomere', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(33679, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100713', 'abnormal monociliated cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(33680, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0103037', 'abnormal ring structure morphology', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(33681, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0131371', 'abnormally decreased number of electrically active cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(33682, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100545', 'abnormal male organism', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(33683, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0141265', 'abnormal escape behavior', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(33684, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0107303', 'abnormal migratory trunk neural crest cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(33685, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0141786', 'abnormal pigment metabolic process', 0.4782608695652174, 4.758907843651163, 1.508641575552437, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(33686, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0102588', 'abnormal centrosome morphology', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(33687, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100186', 'abnormal uveal tract', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(33688, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0125384', 'absent ciliated cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(33689, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0126737', 'abnormally localised mesenchymal stem cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(33690, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0126697', 'abnormally localised proepicardium', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(33691, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100721', 'abnormal centromere', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(33692, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0141911', 'abnormal ribose phosphate metabolic process', 0.4230769230769231, 4.758907843651163, 1.418937661667548, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(33693, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0136521', 'increased cell population proliferation in ventral region', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(33694, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100991', 'abnormal iliac process primordium', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(33695, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100960', 'abnormal postmigratory neural crest cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(33696, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100704', 'abnormal Merkel cell', 0.6190476190476191, 3.6715585125471644, 1.5076039119696991, 'UPHENO:0086172', 'abnormal cell'),
(33697, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0101212', 'abnormal glomeral mesenchyme', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(33698, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0131351', 'abnormally decreased number of apoptotic cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(33699, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0103129', 'abnormal ciliary axoneme morphology', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(33700, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100531', 'abnormal proliferative region', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(33701, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0141263', 'abnormal visually guided collision avoidance behavior', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(33702, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0102323', 'abnormal keratin accumulating cell morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(33703, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0115509', 'abnormally semi-viable whole organism', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(33704, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0127683', 'abnormally localised centromere', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(33705, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0138837', 'decreased cell population proliferation in process', 0.4166666666666667, 5.835653092541957, 1.5593338712067029, 'HP:0011017', 'Abnormal cellular physiology'),
(33706, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0131723', 'abnormal pathway-restricted SMAD protein phosphorylation', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(33707, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0101435', 'abnormal paracrine cell', 0.6190476190476191, 3.6715585125471644, 1.5076039119696991, 'UPHENO:0086172', 'abnormal cell'),
(33708, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0142023', 'absent desmosome', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(33709, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100701', 'abnormal microglial cell', 0.48148148148148145, 3.6715585125471644, 1.3295816755533123, 'UPHENO:0086172', 'abnormal cell'),
(33710, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0141272', 'absent surface breathing', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(33711, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0131553', 'abnormally localised Roux spot', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(33712, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100503', 'abnormal blastomere D2', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(33713, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0125779', 'absent endoplasmic reticulum', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(33714, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0127089', 'abnormally localised myoblast', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(33715, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0131205', 'abnormally decreased number of ciliated cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(33716, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0101016', 'abnormal egg', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(33717, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100225', 'abnormal endocrine system', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(33718, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0101269', 'abnormal mesodermal cell', 0.48148148148148145, 3.6715585125471644, 1.3295816755533123, 'UPHENO:0086172', 'abnormal cell'),
(33719, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0127522', 'abnormally localised cementoblast', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(33720, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0127740', 'abnormally localised yolk platelet', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(33721, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0102285', 'abnormal myoblast morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(33722, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0139130', 'decreased cell population proliferation in interdigital region', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(33723, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0135615', 'increased cell population proliferation in acellular anatomical structure', 0.4166666666666667, 5.835653092541957, 1.5593338712067029, 'HP:0011017', 'Abnormal cellular physiology'),
(33724, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0131061', 'abnormally increased number of keratin accumulating cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(33725, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0101570', 'abnormal forelimb region', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(33726, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0127399', 'abnormally localised melanoblast', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(33727, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0101347', 'abnormal hindlimb region', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(33728, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0139717', 'abnormally necrotic cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(33729, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100862', 'abnormal blastomere V1', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(33730, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0101110', 'abnormal cell-free extract', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(33731, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0131283', 'abnormally decreased number of myoblast', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(33732, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0127364', 'abnormally localised multiciliated cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(33733, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100108', 'abnormal cell part', 0.6190476190476191, 3.6715585125471644, 1.5076039119696991, 'UPHENO:0086172', 'abnormal cell'),
(33734, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0125115', 'absent paracrine cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(33735, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0126982', 'abnormally localised secondary oogonium', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(33736, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100162', 'abnormal presumptive rhombomere', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(33737, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0139669', 'decreased cell population proliferation in ventro-lateral region', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(33738, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100843', 'abnormal fasciculated network of fibrils', 0.5, 3.6715585125471644, 1.3549093166236559, 'UPHENO:0086172', 'abnormal cell'),
(33739, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0101350', 'abnormal blastomere D2.1.2', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(33740, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0127257', 'abnormally localised wedge region', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(33741, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0141777', 'abnormal catabolic process', 0.4782608695652174, 4.758907843651163, 1.508641575552437, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(33742, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0107312', 'abnormal filopodium', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(33743, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0139624', 'decreased cell population proliferation in medial region', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(33744, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0126133', 'absent mitotic cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(33745, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100859', 'abnormal blastomere V1.1.2', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(33746, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0102958', 'abnormal cementoblast morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(33747, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0131735', 'abnormal spindle assembly', 0.5172413793103449, 5.835653092541957, 1.7373661832679608, 'HP:0011017', 'Abnormal cellular physiology'),
(33748, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100786', 'abnormal presumptive axial mesoderm', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(33749, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0125577', 'absent cilium', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(33750, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0131004', 'abnormally increased number of proepicardium', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(33751, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0138844', 'decreased cell population proliferation in extracellular matrix', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(33752, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0125523', 'absent acid secreting cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(33753, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0135716', 'increased cell population proliferation in portion of organism substance', 0.4411764705882353, 5.835653092541957, 1.6045413160604438, 'HP:0011017', 'Abnormal cellular physiology'),
(33754, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0131677', 'abnormal actin filament', 0.5652173913043478, 3.6715585125471644, 1.440565418328227, 'UPHENO:0086172', 'abnormal cell'),
(33755, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100218', 'abnormal epithelial cell', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(33756, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0101503', 'abnormal organ cortex', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(33757, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0133441', 'abnormally increased number of cilium in the ciliated cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(33758, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0127486', 'abnormally localised kinetochore', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(33759, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:00000000', 'Xenopus phenotype', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(33760, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100899', 'abnormal secondary spermatogonium', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(33761, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0131347', 'abnormally decreased number of myelin accumulating cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(33762, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0141299', 'abnormal actin filament morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(33763, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100900', 'abnormal angioblast', 0.52, 3.6715585125471644, 1.3817418089225373, 'UPHENO:0086172', 'abnormal cell'),
(33764, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100026', 'abnormal germ cell', 0.6190476190476191, 3.6715585125471644, 1.5076039119696991, 'UPHENO:0086172', 'abnormal cell'),
(33765, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0135742', 'increased cell population proliferation in extracellular matrix', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(33766, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100003', 'abnormal organism subdivision', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(33767, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0141782', 'abnormal methylation', 0.4782608695652174, 4.758907843651163, 1.508641575552437, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(33768, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0101917', 'abnormal progenitor cell morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(33769, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0131308', 'abnormally decreased number of oxygen accumulating cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(33770, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0101240', 'abnormal ciliated non-epidermal cell', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(33771, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0136519', 'increased cell population proliferation in posterior region', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(33772, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0125559', 'absent electrically active cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(33773, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100864', 'abnormal dorsolateral ascending neuron', 0.48148148148148145, 3.6715585125471644, 1.3295816755533123, 'UPHENO:0086172', 'abnormal cell'),
(33774, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0126159', 'absent apoptotic cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(33775, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0101468', 'abnormal stage I oocyte', 0.5652173913043478, 3.6715585125471644, 1.440565418328227, 'UPHENO:0086172', 'abnormal cell'),
(33776, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0103644', 'abnormally decreased number of cilium in the multiciliated cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(33777, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0107265', 'abnormal posterior side', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(33778, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0127653', 'abnormally localised Merkel cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(33779, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0141794', 'abnormal prosthetic group metabolic process', 0.4782608695652174, 4.758907843651163, 1.508641575552437, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(33780, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0135322', 'increased cell population proliferation in marginal zone (sensu neural)', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(33781, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0107263', 'abnormal anatomical side', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(33782, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100437', 'abnormal proepicardium', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(33783, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100574', 'abnormal gastrula cell', 0.5652173913043478, 3.6715585125471644, 1.440565418328227, 'UPHENO:0086172', 'abnormal cell'),
(33784, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0102386', 'abnormal electrically active cell morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(33785, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0101362', 'abnormal vegetal cortex', 0.52, 3.6715585125471644, 1.3817418089225373, 'UPHENO:0086172', 'abnormal cell'),
(33786, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0126983', 'abnormally localised primordial germ cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(33787, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0131248', 'abnormally decreased number of acid secreting cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(33788, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0131352', 'abnormally decreased number of barrier cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(33789, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0101166', 'abnormal premigratory neural crest cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(33790, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0115758', 'abnormally decreased mobility of melanoblast', 0.52, 3.6715585125471644, 1.3817418089225373, 'UPHENO:0086172', 'abnormal cell'),
(33791, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100887', 'abnormal right-dorsal blastomere', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(33792, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0126600', 'abnormally localised progenitor cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(33793, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0141907', 'abnormal putrescine metabolic process', 0.44, 4.758907843651163, 1.447038165082909, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(33794, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0141880', 'abnormal ethanolamine metabolic process', 0.4074074074074074, 4.758907843651163, 1.392413123563799, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(33795, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0131082', 'abnormally increased number of alkali secreting cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(33796, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0103005', 'abnormal oxygen accumulating cell morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(33797, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0142030', 'abnormally localised desmosome', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(33798, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100814', 'abnormal natural killer cell', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(33799, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0138838', 'decreased cell population proliferation in cell condensation', 0.4166666666666667, 5.835653092541957, 1.5593338712067029, 'HP:0011017', 'Abnormal cellular physiology'),
(33800, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0131669', 'abnormal Roux spot', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(33801, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0101221', 'abnormal larval immune system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(33802, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100675', 'abnormal dorsal vegetal hemisphere blastomere', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(33803, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0127337', 'abnormally localised oxygen accumulating cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(33804, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0131691', 'abnormal molecular function', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(33805, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100901', 'abnormal blastomere D1.2.2', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(33806, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0139619', 'decreased cell population proliferation in basal region', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(33807, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0131292', 'abnormally decreased number of mucus secreting cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(33808, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100626', 'abnormal primordial germ cell', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(33809, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0103067', 'abnormal paracrine cell morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(33810, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0138579', 'decreased cell population proliferation in whole organism', 0.42857142857142855, 5.835653092541957, 1.5814531869511603, 'HP:0011017', 'Abnormal cellular physiology'),
(33811, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0101490', 'abnormal ectodermal cell', 0.48148148148148145, 3.6715585125471644, 1.3295816755533123, 'UPHENO:0086172', 'abnormal cell'),
(33812, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0135478', 'increased cell population proliferation in female organism', 0.4166666666666667, 5.835653092541957, 1.5593338712067029, 'HP:0011017', 'Abnormal cellular physiology'),
(33813, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0101061', 'abnormal plasma membrane', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(33814, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0103636', 'abnormally increased number of melanoblast', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(33815, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0141718', 'abnormal posterior notochord', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(33816, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100642', 'abnormal gustatory system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(33817, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0107287', 'abnormal afferent neuron', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(33818, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100308', 'abnormal early embryonic cell', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(33819, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0136478', 'increased cell population proliferation in thoracic region', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(33820, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0125833', 'absent kinetochore', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(33821, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0139623', 'decreased cell population proliferation in ventral region', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(33822, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0101409', 'abnormal perivitelline space', 0.5652173913043478, 3.6715585125471644, 1.440565418328227, 'UPHENO:0086172', 'abnormal cell'),
(33823, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100999', 'abnormal serous membrane', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(33824, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100398', 'abnormal vegetal blastomere', 0.48148148148148145, 3.6715585125471644, 1.3295816755533123, 'UPHENO:0086172', 'abnormal cell'),
(33825, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0101461', 'abnormal sperm entry point', 0.5652173913043478, 3.6715585125471644, 1.440565418328227, 'UPHENO:0086172', 'abnormal cell'),
(33826, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0127018', 'abnormally localised ciliated cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(33827, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0101074', 'abnormal germinal vesicle', 0.52, 3.6715585125471644, 1.3817418089225373, 'UPHENO:0086172', 'abnormal cell'),
(33828, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0141877', 'abnormal 2-deoxyribose 1-phosphate metabolic process', 0.4230769230769231, 4.758907843651163, 1.418937661667548, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(33829, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0136321', 'increased cell population proliferation in multicellular anatomical structure', 0.4166666666666667, 5.835653092541957, 1.5593338712067029, 'HP:0011017', 'Abnormal cellular physiology'),
(33830, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0131550', 'abnormally localised adherens junction', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(33831, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0126681', 'abnormally localised basal body', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(33832, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100917', 'abnormal stage III oocyte', 0.5652173913043478, 3.6715585125471644, 1.440565418328227, 'UPHENO:0086172', 'abnormal cell'),
(33833, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0101094', 'abnormal blastomere V2.2.1', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(33834, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0102069', 'abnormal proepicardium morphology', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(33835, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100417', 'abnormal dense regular connective tissue', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(33836, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0103167', 'abnormal absorptive cell morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(33837, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0107268', 'abnormal left side', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(33838, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0102109', 'abnormal pericyte morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(33839, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0101113', 'abnormal stage IV oocyte', 0.5652173913043478, 3.6715585125471644, 1.440565418328227, 'UPHENO:0086172', 'abnormal cell'),
(33840, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0107278', 'abnormal medial region', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(33841, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0125715', 'absent barrier cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(33842, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0128071', 'decreased size of the cell part', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(33843, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0133445', 'abnormally increased number of cilium in the ciliated non-epidermal cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(33844, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100802', 'abnormal exocrine cell', 0.6190476190476191, 3.6715585125471644, 1.5076039119696991, 'UPHENO:0086172', 'abnormal cell'),
(33845, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0125750', 'absent melanoblast', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(33846, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100002', 'abnormal head', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(33847, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0102434', 'abnormal exocrine cell morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(33848, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0135475', 'increased cell population proliferation in anatomical group', 0.4166666666666667, 5.835653092541957, 1.5593338712067029, 'HP:0011017', 'Abnormal cellular physiology'),
(33849, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100060', 'abnormal regenerating tissue', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(33850, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0135507', 'increased cell population proliferation in tissue', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(33851, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0141781', 'abnormal secondary metabolic process', 0.4782608695652174, 4.758907843651163, 1.508641575552437, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(33852, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0131720', 'abnormal mitotic spindle assembly', 0.45454545454545453, 5.835653092541957, 1.6286711109119212, 'HP:0011017', 'Abnormal cellular physiology'),
(33853, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0126630', 'abnormally localised early embryonic cell', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(33854, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0125824', 'absent nucleus', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(33855, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0124716', 'absent cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(33856, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0135788', 'increased cell population proliferation in intersomitic region', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(33857, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0127435', 'abnormally localised mitotic spindle', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(33858, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0127196', 'abnormally localised electrically active cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(33859, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100172', 'abnormal stem cell', 0.6190476190476191, 3.6715585125471644, 1.5076039119696991, 'UPHENO:0086172', 'abnormal cell'),
(33860, 'HP:0034687', 'Impaired cerebroside sulfate hydrolysis', 'XPO:0100907', 'abnormal cytoplasm', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(33861, 'HP:0002101', 'Abnormal lung lobation', 'XPO:0141614', 'metaplastic larynx', 0.48, 7.241224942262181, 1.8643465268790154, 'HP:0012252', 'Abnormal respiratory system morphology'),
(33862, 'HP:0002101', 'Abnormal lung lobation', 'XPO:0100804', 'abnormal larynx', 0.5106382978723404, 7.241224942262181, 1.922926618211807, 'HP:0012252', 'Abnormal respiratory system morphology'),
(33863, 'HP:0002101', 'Abnormal lung lobation', 'XPO:0102436', 'abnormal larynx morphology', 0.43636363636363634, 7.241224942262181, 1.777584666769093, 'HP:0012252', 'Abnormal respiratory system morphology'),
(33864, 'HP:0002101', 'Abnormal lung lobation', 'XPO:0141593', 'edematous lung', 0.4426229508196721, 9.627087342903641, 2.064260111399415, 'HP:0002088', 'Abnormal lung morphology'),
(33865, 'HP:0002101', 'Abnormal lung lobation', 'XPO:0102932', 'abnormal lung morphology', 0.46551724137931033, 9.627087342903641, 2.116973108564721, 'HP:0002088', 'Abnormal lung morphology'),
(33866, 'HP:0002101', 'Abnormal lung lobation', 'XPO:0126197', 'absent larynx', 0.41379310344827586, 7.241224942262181, 1.7310022939400542, 'HP:0012252', 'Abnormal respiratory system morphology'),
(33867, 'HP:0002101', 'Abnormal lung lobation', 'XPO:0101548', 'abnormal pulmonary vein', 0.47368421052631576, 9.627087342903641, 2.135462307719618, 'HP:0002088', 'Abnormal lung morphology'),
(33868, 'HP:0002101', 'Abnormal lung lobation', 'XPO:0102668', 'abnormal pharynx morphology', 0.4067796610169492, 7.241224942262181, 1.7162700916117157, 'HP:0012252', 'Abnormal respiratory system morphology'),
(33869, 'HP:0002101', 'Abnormal lung lobation', 'XPO:0101949', 'abnormal respiratory system morphology', 0.5714285714285714, 7.241224942262181, 2.034168828821693, 'HP:0012252', 'Abnormal respiratory system morphology'),
(33870, 'HP:0002101', 'Abnormal lung lobation', 'XPO:0100875', 'abnormal oropharynx', 0.4444444444444444, 7.241224942262181, 1.793968281927239, 'HP:0012252', 'Abnormal respiratory system morphology'),
(33871, 'HP:0002101', 'Abnormal lung lobation', 'XPO:0100210', 'abnormal pulmonary artery', 0.47368421052631576, 9.627087342903641, 2.135462307719618, 'UPHENO:0019970', 'abnormal lung morphology'),
(33872, 'HP:0002101', 'Abnormal lung lobation', 'XPO:0101036', 'abnormal pharynx', 0.47058823529411764, 7.241224942262181, 1.8459781328463531, 'HP:0012252', 'Abnormal respiratory system morphology'),
(33873, 'HP:0002101', 'Abnormal lung lobation', 'XPO:0139850', 'abnormally necrotic respiratory system', 0.5106382978723404, 7.241224942262181, 1.922926618211807, 'HP:0012252', 'Abnormal respiratory system morphology'),
(33874, 'HP:0002101', 'Abnormal lung lobation', 'XPO:0127882', 'abnormally localised pulmonary vein', 0.40298507462686567, 9.627087342903641, 1.9696630451220274, 'HP:0002088', 'Abnormal lung morphology'),
(33875, 'HP:0002101', 'Abnormal lung lobation', 'XPO:0141644', 'neoplastic larynx', 0.41379310344827586, 7.241224942262181, 1.7310022939400542, 'HP:0012252', 'Abnormal respiratory system morphology'),
(33876, 'HP:0002101', 'Abnormal lung lobation', 'XPO:0141648', 'neoplastic lung', 0.4426229508196721, 9.627087342903641, 2.064260111399415, 'UPHENO:0019970', 'abnormal lung morphology'),
(33877, 'HP:0002101', 'Abnormal lung lobation', 'XPO:0127859', 'abnormally localised larynx', 0.42105263157894735, 7.241224942262181, 1.746120504946495, 'HP:0012252', 'Abnormal respiratory system morphology'),
(33878, 'HP:0002101', 'Abnormal lung lobation', 'XPO:0130015', 'increased size of the respiratory system', 0.4897959183673469, 7.241224942262181, 1.8832743880539138, 'HP:0012252', 'Abnormal respiratory system morphology'),
(33879, 'HP:0002101', 'Abnormal lung lobation', 'XPO:0100586', 'abnormal thyroid primordium', 0.43636363636363634, 7.241224942262181, 1.777584666769093, 'HP:0012252', 'Abnormal respiratory system morphology'),
(33880, 'HP:0002101', 'Abnormal lung lobation', 'XPO:0127602', 'abnormally localised pulmonary artery', 0.40298507462686567, 9.627087342903641, 1.9696630451220274, 'HP:0002088', 'Abnormal lung morphology'),
(33881, 'HP:0002101', 'Abnormal lung lobation', 'XPO:0128535', 'decreased size of the respiratory system', 0.4897959183673469, 7.241224942262181, 1.8832743880539138, 'HP:0012252', 'Abnormal respiratory system morphology'),
(33882, 'HP:0002101', 'Abnormal lung lobation', 'XPO:0126855', 'abnormally localised pharynx', 0.4067796610169492, 7.241224942262181, 1.7162700916117157, 'HP:0012252', 'Abnormal respiratory system morphology'),
(33883, 'HP:0002101', 'Abnormal lung lobation', 'XPO:0101329', 'abnormal pharyngeal epithelium', 0.46153846153846156, 7.241224942262181, 1.8281421770490451, 'HP:0012252', 'Abnormal respiratory system morphology'),
(33884, 'HP:0010944', 'Abnormal renal pelvis morphology', 'XPO:0126072', 'absent mesonephric sinus', 0.4418604651162791, 6.880013295263146, 1.7435612620872136, 'HP:0000077', 'Abnormality of the kidney'),
(33885, 'HP:0010944', 'Abnormal renal pelvis morphology', 'XPO:0101550', 'abnormal pronephric sinus', 0.40425531914893614, 6.880013295263146, 1.6677175931270638, 'HP:0000077', 'Abnormality of the kidney'),
(33886, 'HP:0010944', 'Abnormal renal pelvis morphology', 'XPO:0141643', 'neoplastic kidney', 0.4791666666666667, 7.603795021646889, 1.9087915324988045, 'HP:0012210', 'Abnormal renal morphology'),
(33887, 'HP:0010944', 'Abnormal renal pelvis morphology', 'XPO:0101489', 'abnormal mesonephric late proximal tubule', 0.40425531914893614, 6.880013295263146, 1.6677175931270638, 'HP:0000077', 'Abnormality of the kidney'),
(33888, 'HP:0010944', 'Abnormal renal pelvis morphology', 'XPO:0107387', 'abnormal embryonic kidney morphology', 0.48936170212765956, 7.603795021646889, 1.9289909472112474, 'HP:0012210', 'Abnormal renal morphology'),
(33889, 'HP:0010944', 'Abnormal renal pelvis morphology', 'XPO:0128275', 'decreased size of the kidney', 0.4107142857142857, 7.603795021646889, 1.7671975670630444, 'HP:0012210', 'Abnormal renal morphology'),
(33890, 'HP:0010944', 'Abnormal renal pelvis morphology', 'XPO:0102198', 'abnormal kidney morphology', 0.5111111111111111, 7.603795021646889, 1.971391417799894, 'HP:0012210', 'Abnormal renal morphology'),
(33891, 'HP:0010944', 'Abnormal renal pelvis morphology', 'XPO:0100778', 'abnormal mesonephric kidney', 0.4523809523809524, 6.880013295263146, 1.76419584142599, 'HP:0000077', 'Abnormality of the kidney'),
(33892, 'HP:0010944', 'Abnormal renal pelvis morphology', 'XPO:0125259', 'absent adult kidney', 0.4107142857142857, 7.603795021646889, 1.7671975670630444, 'HP:0012210', 'Abnormal renal morphology'),
(33893, 'HP:0010944', 'Abnormal renal pelvis morphology', 'XPO:0125089', 'absent kidney', 0.42592592592592593, 7.603795021646889, 1.7996259153351557, 'HP:0012210', 'Abnormal renal morphology'),
(33894, 'HP:0010944', 'Abnormal renal pelvis morphology', 'XPO:0129202', 'decreased size of the mesonephric sinus', 0.5348837209302325, 7.603795021646889, 2.0167166817302986, 'HP:0012210', 'Abnormal renal morphology'),
(33895, 'HP:0010944', 'Abnormal renal pelvis morphology', 'XPO:0100270', 'abnormal mesonephric tubule', 0.41304347826086957, 6.880013295263146, 1.685747496500148, 'HP:0000077', 'Abnormality of the kidney'),
(33896, 'HP:0010944', 'Abnormal renal pelvis morphology', 'XPO:0126656', 'abnormally localised embryonic kidney', 0.45098039215686275, 7.603795021646889, 1.8517997895946297, 'HP:0012210', 'Abnormal renal morphology'),
(33897, 'HP:0010944', 'Abnormal renal pelvis morphology', 'XPO:0141613', 'metaplastic kidney', 0.475, 6.880013295263146, 1.8077627928602786, 'HP:0000077', 'Abnormality of the kidney'),
(33898, 'HP:0010944', 'Abnormal renal pelvis morphology', 'XPO:0100761', 'abnormal ureter', 0.4722222222222222, 6.828345551150745, 1.7956883110010016, 'HP:0010935', 'Abnormality of the upper urinary tract'),
(33899, 'HP:0010944', 'Abnormal renal pelvis morphology', 'XPO:0101277', 'abnormal glomerulus', 0.4318181818181818, 6.880013295263146, 1.7236341932224046, 'HP:0000077', 'Abnormality of the kidney'),
(33900, 'HP:0010944', 'Abnormal renal pelvis morphology', 'XPO:0100566', 'abnormal kidney', 0.5277777777777778, 6.880013295263146, 1.9055492982485522, 'HP:0000077', 'Abnormality of the kidney'),
(33901, 'HP:0010944', 'Abnormal renal pelvis morphology', 'XPO:0101565', 'abnormal mesonephric early distal tubule', 0.40425531914893614, 6.880013295263146, 1.6677175931270638, 'HP:0000077', 'Abnormality of the kidney'),
(33902, 'HP:0010944', 'Abnormal renal pelvis morphology', 'XPO:0107388', 'abnormal adult kidney morphology', 0.48936170212765956, 7.603795021646889, 1.9289909472112474, 'HP:0012210', 'Abnormal renal morphology'),
(33903, 'HP:0010944', 'Abnormal renal pelvis morphology', 'XPO:0100567', 'abnormal mesonephric collecting duct', 0.46, 7.603795021646889, 1.870226111986882, 'HP:0012210', 'Abnormal renal morphology'),
(33904, 'HP:0010944', 'Abnormal renal pelvis morphology', 'XPO:0125038', 'absent embryonic kidney', 0.4107142857142857, 7.603795021646889, 1.7671975670630444, 'HP:0012210', 'Abnormal renal morphology'),
(33905, 'HP:0010944', 'Abnormal renal pelvis morphology', 'XPO:0130678', 'increased size of the mesonephric sinus', 0.5348837209302325, 7.603795021646889, 2.0167166817302986, 'HP:0012210', 'Abnormal renal morphology'),
(33906, 'HP:0010944', 'Abnormal renal pelvis morphology', 'XPO:0101701', 'abnormal urinary system morphology', 0.4473684210526316, 7.340144605965611, 1.8121117246651284, 'UPHENO:0087427', 'abnormal renal system morphology'),
(33907, 'HP:0010944', 'Abnormal renal pelvis morphology', 'XPO:0100085', 'abnormal mesonephric sinus', 0.59375, 6.880013295263146, 2.0211402460152272, 'HP:0000077', 'Abnormality of the kidney'),
(33908, 'HP:0010944', 'Abnormal renal pelvis morphology', 'XPO:0100501', 'abnormal urogenital system', 0.43333333333333335, 5.4478002382576385, 1.5364613358553185, 'HP:0000119', 'Abnormality of the genitourinary system'),
(33909, 'HP:0010944', 'Abnormal renal pelvis morphology', 'XPO:0127342', 'abnormally localised mesonephric mesenchyme', 0.41304347826086957, 6.880013295263146, 1.685747496500148, 'HP:0000077', 'Abnormality of the kidney'),
(33910, 'HP:0010944', 'Abnormal renal pelvis morphology', 'XPO:0126885', 'abnormally localised adult kidney', 0.45098039215686275, 7.603795021646889, 1.8517997895946297, 'HP:0012210', 'Abnormal renal morphology'),
(33911, 'HP:0010944', 'Abnormal renal pelvis morphology', 'XPO:0102393', 'abnormal ureter morphology', 0.4222222222222222, 7.340144605965611, 1.760446581684107, 'UPHENO:0087427', 'abnormal renal system morphology'),
(33912, 'HP:0010944', 'Abnormal renal pelvis morphology', 'XPO:0100408', 'abnormal glomus', 0.40425531914893614, 6.880013295263146, 1.6677175931270638, 'HP:0000077', 'Abnormality of the kidney'),
(33913, 'HP:0010944', 'Abnormal renal pelvis morphology', 'XPO:0107300', 'abnormal embryonic kidney', 0.5135135135135135, 6.880013295263146, 1.8796222493549772, 'HP:0000077', 'Abnormality of the kidney'),
(33914, 'HP:0010944', 'Abnormal renal pelvis morphology', 'XPO:0139936', 'abnormally necrotic embryonic kidney', 0.4107142857142857, 7.603795021646889, 1.7671975670630444, 'HP:0012210', 'Abnormal renal morphology'),
(33915, 'HP:0010944', 'Abnormal renal pelvis morphology', 'XPO:0103182', 'abnormal pronephric sinus morphology', 0.4339622641509434, 7.603795021646889, 1.816524181984252, 'HP:0012210', 'Abnormal renal morphology'),
(33916, 'HP:0010944', 'Abnormal renal pelvis morphology', 'XPO:0107301', 'abnormal adult kidney', 0.5135135135135135, 6.880013295263146, 1.8796222493549772, 'HP:0000077', 'Abnormality of the kidney'),
(33917, 'HP:0010944', 'Abnormal renal pelvis morphology', 'XPO:0140354', 'abnormally necrotic adult kidney', 0.4107142857142857, 7.603795021646889, 1.7671975670630444, 'HP:0012210', 'Abnormal renal morphology'),
(33918, 'HP:0010944', 'Abnormal renal pelvis morphology', 'XPO:0128342', 'decreased size of the mesonephric mesenchyme', 0.42592592592592593, 7.603795021646889, 1.7996259153351557, 'HP:0012210', 'Abnormal renal morphology'),
(33919, 'HP:0010944', 'Abnormal renal pelvis morphology', 'XPO:0126884', 'abnormally localised mesonephric kidney', 0.40350877192982454, 7.603795021646889, 1.7516272409365097, 'HP:0012210', 'Abnormal renal morphology'),
(33920, 'HP:0010944', 'Abnormal renal pelvis morphology', 'XPO:0100069', 'abnormal urinary system', 0.4838709677419355, 6.355235291121788, 1.7536002539184354, 'HP:0000079', 'Abnormality of the urinary system'),
(33921, 'HP:0010944', 'Abnormal renal pelvis morphology', 'XPO:0129755', 'increased size of the kidney', 0.40350877192982454, 7.603795021646889, 1.7516272409365097, 'HP:0012210', 'Abnormal renal morphology'),
(33922, 'HP:0010944', 'Abnormal renal pelvis morphology', 'XPO:0101111', 'abnormal mesonephric late distal tubule', 0.40425531914893614, 6.880013295263146, 1.6677175931270638, 'HP:0000077', 'Abnormality of the kidney'),
(33923, 'HP:0010944', 'Abnormal renal pelvis morphology', 'XPO:0100950', 'abnormal pronephric nephron', 0.40425531914893614, 6.880013295263146, 1.6677175931270638, 'HP:0000077', 'Abnormality of the kidney'),
(33924, 'HP:0010944', 'Abnormal renal pelvis morphology', 'XPO:0140552', 'abnormally necrotic kidney', 0.4339622641509434, 7.603795021646889, 1.816524181984252, 'HP:0012210', 'Abnormal renal morphology'),
(33925, 'HP:0010944', 'Abnormal renal pelvis morphology', 'XPO:0100271', 'abnormal mesonephric nephron', 0.4418604651162791, 6.880013295263146, 1.7435612620872136, 'HP:0000077', 'Abnormality of the kidney'),
(33926, 'HP:0010944', 'Abnormal renal pelvis morphology', 'XPO:0100565', 'abnormal pronephric kidney', 0.41304347826086957, 6.880013295263146, 1.685747496500148, 'HP:0000077', 'Abnormality of the kidney'),
(33927, 'HP:0010944', 'Abnormal renal pelvis morphology', 'XPO:0100147', 'abnormal mesonephric mesenchyme', 0.5428571428571428, 6.880013295263146, 1.9325797164116434, 'HP:0000077', 'Abnormality of the kidney'),
(33928, 'HP:0010944', 'Abnormal renal pelvis morphology', 'XPO:0140815', 'abnormally necrotic mesonephric mesenchyme', 0.4423076923076923, 7.603795021646889, 1.833907584586899, 'HP:0012210', 'Abnormal renal morphology'),
(33929, 'HP:0010944', 'Abnormal renal pelvis morphology', 'XPO:0126710', 'abnormally localised kidney', 0.46938775510204084, 7.603795021646889, 1.8892136659115366, 'HP:0012210', 'Abnormal renal morphology'),
(33930, 'HP:0010944', 'Abnormal renal pelvis morphology', 'XPO:0101247', 'abnormal mesonephric early proximal tubule', 0.40425531914893614, 6.880013295263146, 1.6677175931270638, 'HP:0000077', 'Abnormality of the kidney'),
(33931, 'HP:0010944', 'Abnormal renal pelvis morphology', 'XPO:0101717', 'abnormal mesonephric sinus morphology', 0.6052631578947368, 7.603795021646889, 2.1452964799267895, 'HP:0012210', 'Abnormal renal morphology'),
(33932, 'HP:0010944', 'Abnormal renal pelvis morphology', 'XPO:0102410', 'abnormal mesonephric kidney morphology', 0.42592592592592593, 7.603795021646889, 1.7996259153351557, 'HP:0012210', 'Abnormal renal morphology'),
(33933, 'HP:0010944', 'Abnormal renal pelvis morphology', 'XPO:0102132', 'abnormal pronephric nephrostome morphology', 0.40350877192982454, 7.603795021646889, 1.7516272409365097, 'HP:0012210', 'Abnormal renal morphology'),
(33934, 'HP:0010944', 'Abnormal renal pelvis morphology', 'XPO:0101779', 'abnormal mesonephric mesenchyme morphology', 0.5, 7.603795021646889, 1.9498455094759288, 'HP:0012210', 'Abnormal renal morphology'),
(33935, 'HP:0010944', 'Abnormal renal pelvis morphology', 'XPO:0127733', 'abnormally localised mesonephric sinus', 0.48717948717948717, 6.880013295263146, 1.83079254667872, 'HP:0000077', 'Abnormality of the kidney'),
(33936, 'HP:0010944', 'Abnormal renal pelvis morphology', 'XPO:0129822', 'increased size of the mesonephric mesenchyme', 0.42592592592592593, 7.603795021646889, 1.7996259153351557, 'HP:0012210', 'Abnormal renal morphology'),
(33937, 'HP:0010944', 'Abnormal renal pelvis morphology', 'XPO:0101903', 'abnormal mesonephric nephron morphology', 0.42592592592592593, 7.603795021646889, 1.7996259153351557, 'HP:0012210', 'Abnormal renal morphology'),
(33938, 'HP:0430002', 'Abnormal lacrimal bone morphology', 'XPO:0130767', 'increased size of the orbital region', 0.5797101449275363, 11.582693223545188, 2.5912554423044774, 'HP:3000030', 'Abnormal morphology of bony orbit of skull'),
(33939, 'HP:0430002', 'Abnormal lacrimal bone morphology', 'XPO:0102564', 'abnormal olfactory region morphology', 0.5, 7.024697770424301, 1.8741261657669024, 'HP:0000929', 'Abnormal skull morphology'),
(33940, 'HP:0430002', 'Abnormal lacrimal bone morphology', 'XPO:0103152', 'abnormal otic region morphology', 0.5, 7.024697770424301, 1.8741261657669024, 'HP:0000929', 'Abnormal skull morphology'),
(33941, 'HP:0430002', 'Abnormal lacrimal bone morphology', 'XPO:0126871', 'abnormally localised choana', 0.4153846153846154, 5.788671267106304, 1.5506530843083268, 'UPHENO:0087472', 'abnormal face morphology'),
(33942, 'HP:0430002', 'Abnormal lacrimal bone morphology', 'XPO:0102215', 'abnormal mandibular arch skeleton morphology', 0.40625, 4.638757693672553, 1.3727692133255593, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(33943, 'HP:0430002', 'Abnormal lacrimal bone morphology', 'XPO:0101659', 'abnormal lower jaw morphology', 0.5070422535211268, 8.057231734572694, 2.0212265919089023, 'UPHENO:0084457', 'abnormal facial skeleton morphology'),
(33944, 'HP:0430002', 'Abnormal lacrimal bone morphology', 'XPO:0130324', 'increased size of the choana', 0.4857142857142857, 7.024697770424301, 1.8471589157190496, 'HP:0000929', 'Abnormal skull morphology'),
(33945, 'HP:0430002', 'Abnormal lacrimal bone morphology', 'XPO:0128477', 'decreased size of the neurocranium', 0.44285714285714284, 7.024697770424301, 1.7637850163909, 'HP:0000929', 'Abnormal skull morphology'),
(33946, 'HP:0430002', 'Abnormal lacrimal bone morphology', 'XPO:0130358', 'increased size of the lower jaw', 0.46153846153846156, 8.057231734572694, 1.9283989055777726, 'UPHENO:0084457', 'abnormal facial skeleton morphology'),
(33947, 'HP:0430002', 'Abnormal lacrimal bone morphology', 'XPO:0129688', 'increased size of the olfactory region', 0.4492753623188406, 7.024697770424301, 1.7765200916363793, 'HP:0000929', 'Abnormal skull morphology'),
(33948, 'HP:0430002', 'Abnormal lacrimal bone morphology', 'XPO:0139784', 'abnormally necrotic cranium', 0.40625, 4.638757693672553, 1.3727692133255593, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(33949, 'HP:0430002', 'Abnormal lacrimal bone morphology', 'XPO:0103138', 'abnormal upper jaw morphology', 0.4931506849315068, 8.057231734572694, 1.9933462691053947, 'UPHENO:0084457', 'abnormal facial skeleton morphology'),
(33950, 'HP:0430002', 'Abnormal lacrimal bone morphology', 'XPO:0102259', 'abnormal pharyngeal region morphology', 0.40384615384615385, 4.5318002188002176, 1.3528303989641963, 'UPHENO:0087907', 'abnormal head morphology'),
(33951, 'HP:0430002', 'Abnormal lacrimal bone morphology', 'XPO:0141829', 'increased width of head', 0.4492753623188406, 7.024697770424301, 1.7765200916363793, 'HP:0000929', 'Abnormal skull morphology'),
(33952, 'HP:0430002', 'Abnormal lacrimal bone morphology', 'XPO:0130425', 'increased size of the otic region', 0.4492753623188406, 7.024697770424301, 1.7765200916363793, 'HP:0000929', 'Abnormal skull morphology'),
(33953, 'HP:0430002', 'Abnormal lacrimal bone morphology', 'XPO:0128880', 'decreased size of the lower jaw', 0.46153846153846156, 8.057231734572694, 1.9283989055777726, 'UPHENO:0084457', 'abnormal facial skeleton morphology'),
(33954, 'HP:0430002', 'Abnormal lacrimal bone morphology', 'XPO:0141201', 'abnormally necrotic sphenoid region', 0.4626865671641791, 7.024697770424301, 1.8028403414510898, 'HP:0000929', 'Abnormal skull morphology'),
(33955, 'HP:0430002', 'Abnormal lacrimal bone morphology', 'XPO:0129225', 'decreased size of the upper jaw', 0.45, 8.057231734572694, 1.904141349941677, 'UPHENO:0084457', 'abnormal facial skeleton morphology'),
(33956, 'HP:0430002', 'Abnormal lacrimal bone morphology', 'XPO:0102921', 'abnormal orbital region morphology', 0.6666666666666666, 11.582693223545188, 2.778811883226977, 'HP:3000030', 'Abnormal morphology of bony orbit of skull'),
(33957, 'HP:0430002', 'Abnormal lacrimal bone morphology', 'XPO:0101997', 'abnormal braincase and otic capsule skeleton morphology', 0.4126984126984127, 4.638757693672553, 1.3836213127410304, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(33958, 'HP:0430002', 'Abnormal lacrimal bone morphology', 'XPO:0140672', 'abnormally necrotic olfactory region', 0.4626865671641791, 7.024697770424301, 1.8028403414510898, 'HP:0000929', 'Abnormal skull morphology'),
(33959, 'HP:0430002', 'Abnormal lacrimal bone morphology', 'XPO:0128846', 'decreased size of the choana', 0.4857142857142857, 7.024697770424301, 1.8471589157190496, 'HP:0000929', 'Abnormal skull morphology'),
(33960, 'HP:0430002', 'Abnormal lacrimal bone morphology', 'XPO:0101681', 'abnormal chondrocranium morphology', 0.4262295081967213, 4.638757693672553, 1.4061206955371255, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(33961, 'HP:0430002', 'Abnormal lacrimal bone morphology', 'XPO:0103381', 'increased size of the head', 0.47692307692307695, 7.024697770424301, 1.8303662133915815, 'HP:0000929', 'Abnormal skull morphology'),
(33962, 'HP:0430002', 'Abnormal lacrimal bone morphology', 'XPO:0102776', 'abnormal fenestra subocularis morphology', 0.43333333333333335, 4.638757693672553, 1.4177899470389728, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(33963, 'HP:0430002', 'Abnormal lacrimal bone morphology', 'XPO:0102052', 'abnormal choana morphology', 0.53125, 7.024697770424301, 1.9318050342976927, 'HP:0000929', 'Abnormal skull morphology'),
(33964, 'HP:0430002', 'Abnormal lacrimal bone morphology', 'XPO:0140897', 'abnormally necrotic lower jaw', 0.47368421052631576, 8.057231734572694, 1.9536078043503626, 'UPHENO:0084457', 'abnormal facial skeleton morphology'),
(33965, 'HP:0430002', 'Abnormal lacrimal bone morphology', 'XPO:0100420', 'abnormal choana', 0.46551724137931033, 5.788671267106304, 1.641562146102, 'UPHENO:0087472', 'abnormal face morphology'),
(33966, 'HP:0430002', 'Abnormal lacrimal bone morphology', 'XPO:0140926', 'abnormally necrotic neurocranium', 0.4626865671641791, 7.024697770424301, 1.8028403414510898, 'HP:0000929', 'Abnormal skull morphology'),
(33967, 'HP:0430002', 'Abnormal lacrimal bone morphology', 'XPO:0102005', 'abnormal splanchnocranium morphology', 0.4262295081967213, 4.638757693672553, 1.4061206955371255, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(33968, 'HP:0430002', 'Abnormal lacrimal bone morphology', 'XPO:0129689', 'increased size of the sphenoid region', 0.4492753623188406, 7.024697770424301, 1.7765200916363793, 'HP:0000929', 'Abnormal skull morphology'),
(33969, 'HP:0430002', 'Abnormal lacrimal bone morphology', 'XPO:0130701', 'increased size of the upper jaw', 0.45, 8.057231734572694, 1.904141349941677, 'UPHENO:0084457', 'abnormal facial skeleton morphology'),
(33970, 'HP:0430002', 'Abnormal lacrimal bone morphology', 'XPO:0129957', 'increased size of the neurocranium', 0.44285714285714284, 7.024697770424301, 1.7637850163909, 'HP:0000929', 'Abnormal skull morphology'),
(33971, 'HP:0430002', 'Abnormal lacrimal bone morphology', 'XPO:0128905', 'decreased size of the occipital region', 0.45588235294117646, 7.024697770424301, 1.78953506483714, 'HP:0000929', 'Abnormal skull morphology'),
(33972, 'HP:0430002', 'Abnormal lacrimal bone morphology', 'XPO:0129291', 'decreased size of the orbital region', 0.5797101449275363, 11.582693223545188, 2.5912554423044774, 'HP:3000030', 'Abnormal morphology of bony orbit of skull'),
(33973, 'HP:0430002', 'Abnormal lacrimal bone morphology', 'XPO:0100584', 'abnormal vertebral column', 0.40350877192982454, 6.272837960958401, 1.5909573036826314, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(33974, 'HP:0430002', 'Abnormal lacrimal bone morphology', 'XPO:0130383', 'increased size of the occipital region', 0.45588235294117646, 7.024697770424301, 1.78953506483714, 'HP:0000929', 'Abnormal skull morphology'),
(33975, 'HP:0430002', 'Abnormal lacrimal bone morphology', 'XPO:0102401', 'abnormal neurocranium morphology', 0.5, 7.024697770424301, 1.8741261657669024, 'HP:0000929', 'Abnormal skull morphology'),
(33976, 'HP:0430002', 'Abnormal lacrimal bone morphology', 'XPO:0128208', 'decreased size of the olfactory region', 0.4492753623188406, 7.024697770424301, 1.7765200916363793, 'HP:0000929', 'Abnormal skull morphology'),
(33977, 'HP:0430002', 'Abnormal lacrimal bone morphology', 'XPO:0103176', 'abnormal fenestra basicranialis morphology', 0.43333333333333335, 4.638757693672553, 1.4177899470389728, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(33978, 'HP:0430002', 'Abnormal lacrimal bone morphology', 'XPO:0102720', 'abnormal dermatocranium morphology', 0.4262295081967213, 4.638757693672553, 1.4061206955371255, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(33979, 'HP:0430002', 'Abnormal lacrimal bone morphology', 'XPO:0140560', 'abnormally necrotic orbital region', 0.6153846153846154, 11.582693223545188, 2.6697960997966392, 'HP:3000030', 'Abnormal morphology of bony orbit of skull'),
(33980, 'HP:0430002', 'Abnormal lacrimal bone morphology', 'XPO:0140644', 'abnormally necrotic otic region', 0.4626865671641791, 7.024697770424301, 1.8028403414510898, 'HP:0000929', 'Abnormal skull morphology'),
(33981, 'HP:0430002', 'Abnormal lacrimal bone morphology', 'XPO:0102092', 'abnormal ethmoid region morphology', 0.43333333333333335, 4.638757693672553, 1.4177899470389728, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(33982, 'HP:0430002', 'Abnormal lacrimal bone morphology', 'XPO:0101483', 'abnormal nostril', 0.4067796610169492, 5.788671267106304, 1.5345076525622334, 'UPHENO:0087472', 'abnormal face morphology'),
(33983, 'HP:0430002', 'Abnormal lacrimal bone morphology', 'XPO:0102665', 'abnormal suspensorium morphology', 0.4262295081967213, 4.638757693672553, 1.4061206955371255, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(33984, 'HP:0430002', 'Abnormal lacrimal bone morphology', 'XPO:0128947', 'decreased size of the otic region', 0.4492753623188406, 7.024697770424301, 1.7765200916363793, 'HP:0000929', 'Abnormal skull morphology'),
(33985, 'HP:0430002', 'Abnormal lacrimal bone morphology', 'XPO:0102351', 'abnormal sphenoid region morphology', 0.5, 7.024697770424301, 1.8741261657669024, 'HP:0000929', 'Abnormal skull morphology'),
(33986, 'HP:0430002', 'Abnormal lacrimal bone morphology', 'XPO:0128209', 'decreased size of the sphenoid region', 0.4492753623188406, 7.024697770424301, 1.7765200916363793, 'HP:0000929', 'Abnormal skull morphology'),
(33987, 'HP:0430002', 'Abnormal lacrimal bone morphology', 'XPO:0140639', 'abnormally necrotic upper jaw', 0.46153846153846156, 8.057231734572694, 1.9283989055777726, 'UPHENO:0084457', 'abnormal facial skeleton morphology'),
(33988, 'HP:0430002', 'Abnormal lacrimal bone morphology', 'XPO:0101764', 'abnormal cranium morphology', 0.4406779661016949, 4.638757693672553, 1.4297546312868548, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(33989, 'HP:0430002', 'Abnormal lacrimal bone morphology', 'XPO:0102828', 'abnormal occipital region morphology', 0.5081967213114754, 7.024697770424301, 1.8894254087244782, 'HP:0000929', 'Abnormal skull morphology'),
(33990, 'HP:0430002', 'Abnormal lacrimal bone morphology', 'XPO:0141185', 'abnormally necrotic occipital region', 0.4696969696969697, 7.024697770424301, 1.8164468766813286, 'HP:0000929', 'Abnormal skull morphology'),
(33991, 'HP:0010898', 'Abnormal circulating sarcosine concentration', 'XPO:0141893', 'abnormal isoleucine metabolic process', 0.5694444444444444, 10.156767408123608, 2.404935503099904, 'UPHENO:0050249', 'abnormal alpha-amino acid metabolic process'),
(33992, 'HP:0010898', 'Abnormal circulating sarcosine concentration', 'XPO:0141905', 'abnormal ornithine metabolic process', 0.5774647887323944, 10.156767408123608, 2.4218124505287704, 'UPHENO:0050249', 'abnormal alpha-amino acid metabolic process'),
(33993, 'HP:0010898', 'Abnormal circulating sarcosine concentration', 'XPO:0141868', 'abnormal asparagine metabolic process', 0.5694444444444444, 10.156767408123608, 2.404935503099904, 'UPHENO:0050249', 'abnormal alpha-amino acid metabolic process'),
(33994, 'HP:0010898', 'Abnormal circulating sarcosine concentration', 'XPO:0141889', 'abnormal homoserine metabolic process', 0.5833333333333334, 13.002596477995848, 2.7540602654077087, 'UPHENO:0078643', 'abnormal serine family amino acid metabolic process'),
(33995, 'HP:0010898', 'Abnormal circulating sarcosine concentration', 'XPO:0141848', 'abnormal proline metabolic process', 0.5694444444444444, 10.156767408123608, 2.404935503099904, 'UPHENO:0050249', 'abnormal alpha-amino acid metabolic process'),
(33996, 'HP:0010898', 'Abnormal circulating sarcosine concentration', 'XPO:0141853', 'abnormal glutamate metabolic process', 0.5540540540540541, 10.156767408123608, 2.372213767465945, 'UPHENO:0050249', 'abnormal alpha-amino acid metabolic process'),
(33997, 'HP:0010898', 'Abnormal circulating sarcosine concentration', 'XPO:0141918', 'abnormal tyrosine metabolic process', 0.5694444444444444, 10.156767408123608, 2.404935503099904, 'UPHENO:0050249', 'abnormal alpha-amino acid metabolic process'),
(33998, 'HP:0010898', 'Abnormal circulating sarcosine concentration', 'XPO:0141913', 'abnormal L-serine metabolic process', 0.5833333333333334, 13.002596477995848, 2.7540602654077087, 'UPHENO:0078643', 'abnormal serine family amino acid metabolic process'),
(33999, 'HP:0010898', 'Abnormal circulating sarcosine concentration', 'XPO:0141843', 'abnormal alanine metabolic process', 0.5774647887323944, 10.156767408123608, 2.4218124505287704, 'UPHENO:0050249', 'abnormal alpha-amino acid metabolic process'),
(34000, 'HP:0010898', 'Abnormal circulating sarcosine concentration', 'XPO:0141917', 'abnormal tryptophan metabolic process', 0.5694444444444444, 10.156767408123608, 2.404935503099904, 'UPHENO:0050249', 'abnormal alpha-amino acid metabolic process'),
(34001, 'HP:0010898', 'Abnormal circulating sarcosine concentration', 'XPO:0141922', 'abnormal valine metabolic process', 0.5694444444444444, 10.156767408123608, 2.404935503099904, 'UPHENO:0050249', 'abnormal alpha-amino acid metabolic process'),
(34002, 'HP:0010898', 'Abnormal circulating sarcosine concentration', 'XPO:0141847', 'abnormal arginine metabolic process', 0.5694444444444444, 10.156767408123608, 2.404935503099904, 'UPHENO:0050249', 'abnormal alpha-amino acid metabolic process'),
(34003, 'HP:0010898', 'Abnormal circulating sarcosine concentration', 'XPO:0141895', 'abnormal leucine metabolic process', 0.5694444444444444, 10.156767408123608, 2.404935503099904, 'UPHENO:0050249', 'abnormal alpha-amino acid metabolic process'),
(34004, 'HP:0010898', 'Abnormal circulating sarcosine concentration', 'XPO:0141858', 'abnormal serine family amino acid metabolic process', 0.6, 13.002596477995848, 2.793126901305687, 'UPHENO:0078643', 'abnormal serine family amino acid metabolic process'),
(34005, 'HP:0010898', 'Abnormal circulating sarcosine concentration', 'XPO:0141912', 'abnormal D-serine metabolic process', 0.5833333333333334, 13.002596477995848, 2.7540602654077087, 'UPHENO:0078643', 'abnormal serine family amino acid metabolic process'),
(34006, 'HP:0010898', 'Abnormal circulating sarcosine concentration', 'XPO:0141888', 'abnormal threonine metabolic process', 0.5694444444444444, 10.156767408123608, 2.404935503099904, 'UPHENO:0050249', 'abnormal alpha-amino acid metabolic process'),
(34007, 'HP:0010898', 'Abnormal circulating sarcosine concentration', 'XPO:0141873', 'abnormal tricarboxylic acid metabolic process', 0.49295774647887325, 9.119292702704945, 2.1202419626558338, 'HP:0004354', 'Abnormal circulating carboxylic acid concentration'),
(34008, 'HP:0010898', 'Abnormal circulating sarcosine concentration', 'XPO:0141887', 'abnormal histidine metabolic process', 0.5694444444444444, 10.156767408123608, 2.404935503099904, 'UPHENO:0050249', 'abnormal alpha-amino acid metabolic process'),
(34009, 'HP:0010898', 'Abnormal circulating sarcosine concentration', 'XPO:0141896', 'abnormal lysine metabolic process', 0.5694444444444444, 10.156767408123608, 2.404935503099904, 'UPHENO:0050249', 'abnormal alpha-amino acid metabolic process'),
(34010, 'HP:0010898', 'Abnormal circulating sarcosine concentration', 'XPO:0141882', 'abnormal gamma-aminobutyric acid metabolic process', 0.5633802816901409, 10.007478699375595, 2.374450708829793, 'UPHENO:0051195', 'abnormal amino acid metabolic process'),
(34011, 'HP:0010898', 'Abnormal circulating sarcosine concentration', 'XPO:0141869', 'abnormal alpha-amino acid metabolic process', 0.5942028985507246, 10.156767408123608, 2.456660463680844, 'UPHENO:0050249', 'abnormal alpha-amino acid metabolic process'),
(34012, 'HP:0010898', 'Abnormal circulating sarcosine concentration', 'XPO:0141857', 'abnormal glycine metabolic process', 0.5833333333333334, 13.002596477995848, 2.7540602654077087, 'UPHENO:0078643', 'abnormal serine family amino acid metabolic process'),
(34013, 'HP:0040210', 'Abnormal circulating biopterin concentration', 'XPO:0100372', 'abnormal hematological system', 0.41935483870967744, 5.574066539846944, 1.5288923359002506, 'HP:0001871', 'Abnormality of blood and blood-forming tissues'),
(34014, 'HP:0001609', 'Hoarse voice', 'XPO:0101220', 'abnormal centriole', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(34015, 'HP:0001609', 'Hoarse voice', 'XPO:0100715', 'abnormal ciliated cell', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(34016, 'HP:0001609', 'Hoarse voice', 'XPO:0100394', 'abnormal marginal zone', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34017, 'HP:0001609', 'Hoarse voice', 'XPO:0100954', 'abnormal neural progenitor cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(34018, 'HP:0001609', 'Hoarse voice', 'XPO:0100726', 'abnormal tail', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34019, 'HP:0001609', 'Hoarse voice', 'XPO:0100734', 'abnormal lateral line system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(34020, 'HP:0001609', 'Hoarse voice', 'XPO:0100189', 'abnormal enteroendocrine cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(34021, 'HP:0001609', 'Hoarse voice', 'XPO:0101029', 'abnormal right spleen primordium', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(34022, 'HP:0001609', 'Hoarse voice', 'XPO:0100588', 'abnormal unicellular gland', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34023, 'HP:0001609', 'Hoarse voice', 'XPO:0100707', 'abnormal central vegetal yolk mass', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34024, 'HP:0001609', 'Hoarse voice', 'XPO:0101237', 'abnormal mucus secreting cell', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(34025, 'HP:0001609', 'Hoarse voice', 'XPO:0100317', 'abnormal respiratory system', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(34026, 'HP:0001609', 'Hoarse voice', 'XPO:0101570', 'abnormal forelimb region', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34027, 'HP:0001609', 'Hoarse voice', 'XPO:0100762', 'abnormal intersomitic region', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34028, 'HP:0001609', 'Hoarse voice', 'XPO:0100724', 'abnormal kinetochore', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(34029, 'HP:0001609', 'Hoarse voice', 'XPO:0100201', 'abnormal cavitated compound organ', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34030, 'HP:0001609', 'Hoarse voice', 'XPO:0101132', 'abnormal apoptotic cell', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(34031, 'HP:0001609', 'Hoarse voice', 'XPO:0100868', 'abnormal transporting epithelium', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34032, 'HP:0001609', 'Hoarse voice', 'XPO:0100104', 'abnormal embryonic structure', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34033, 'HP:0001609', 'Hoarse voice', 'XPO:0100493', 'abnormal liver and biliary system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(34034, 'HP:0001609', 'Hoarse voice', 'XPO:0100796', 'abnormal pseudoblastema', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34035, 'HP:0001609', 'Hoarse voice', 'XPO:0100282', 'abnormal pelvic girdle primordium', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34036, 'HP:0001609', 'Hoarse voice', 'XPO:0101373', 'abnormal oxygen accumulating cell', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(34037, 'HP:0001609', 'Hoarse voice', 'XPO:0107265', 'abnormal posterior side', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34038, 'HP:0001609', 'Hoarse voice', 'XPO:0141276', 'decreased surface breathing', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(34039, 'HP:0001609', 'Hoarse voice', 'XPO:0100468', 'abnormal muscular system', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34040, 'HP:0001609', 'Hoarse voice', 'XPO:0100721', 'abnormal centromere', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(34041, 'HP:0001609', 'Hoarse voice', 'XPO:0107273', 'abnormal basal region', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34042, 'HP:0001609', 'Hoarse voice', 'XPO:0100784', 'abnormal left blastomere', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(34043, 'HP:0001609', 'Hoarse voice', 'XPO:0101368', 'abnormal regenerating eye', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34044, 'HP:0001609', 'Hoarse voice', 'XPO:0100581', 'abnormal immune system', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(34045, 'HP:0001609', 'Hoarse voice', 'XPO:0100846', 'abnormal hindlimb', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(34046, 'HP:0001609', 'Hoarse voice', 'XPO:0100484', 'abnormal cement gland primordium', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34047, 'HP:0001609', 'Hoarse voice', 'XPO:0107268', 'abnormal left side', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34048, 'HP:0001609', 'Hoarse voice', 'XPO:0124719', 'absent anatomical structure', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34049, 'HP:0001609', 'Hoarse voice', 'XPO:0107312', 'abnormal filopodium', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(34050, 'HP:0001609', 'Hoarse voice', 'XPO:0100084', 'abnormal anatomical group', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34051, 'HP:0001609', 'Hoarse voice', 'XPO:0101405', 'abnormal ring structure', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(34052, 'HP:0001609', 'Hoarse voice', 'XPO:0141714', 'abnormal anterior notochord', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(34053, 'HP:0001609', 'Hoarse voice', 'XPO:0101071', 'abnormal endoplasmic reticulum', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(34054, 'HP:0001609', 'Hoarse voice', 'XPO:0101302', 'abnormal subcortical cytoplasm', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(34055, 'HP:0001609', 'Hoarse voice', 'XPO:0101451', 'abnormal dorsal lymph space', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(34056, 'HP:0001609', 'Hoarse voice', 'XPO:0100605', 'abnormal prechordal plate', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34057, 'HP:0001609', 'Hoarse voice', 'XPO:0101110', 'abnormal cell-free extract', 0.5294117647058824, 1.706362323152461, 0.9504568842024205, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34058, 'HP:0001609', 'Hoarse voice', 'XPO:0100741', 'abnormal blastopore', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34059, 'HP:0001609', 'Hoarse voice', 'XPO:0100273', 'abnormal visual system', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(34060, 'HP:0001609', 'Hoarse voice', 'XPO:0100162', 'abnormal presumptive rhombomere', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34061, 'HP:0001609', 'Hoarse voice', 'XPO:0101569', 'abnormal activin-induced ectoderm', 0.5294117647058824, 1.706362323152461, 0.9504568842024205, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34062, 'HP:0001609', 'Hoarse voice', 'XPO:0100985', 'abnormal simple columnar epithelium', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34063, 'HP:0001609', 'Hoarse voice', 'XPO:0100482', 'abnormal Mullerian duct', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(34064, 'HP:0001609', 'Hoarse voice', 'XPO:0141271', 'increased surface breathing', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(34065, 'HP:0001609', 'Hoarse voice', 'XPO:0100031', 'abnormal central nervous system', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(34066, 'HP:0001609', 'Hoarse voice', 'XPO:0100781', 'abnormal presumptive ectoderm', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34067, 'HP:0001609', 'Hoarse voice', 'XPO:0101490', 'abnormal ectodermal cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(34068, 'HP:0001609', 'Hoarse voice', 'XPO:0100899', 'abnormal secondary spermatogonium', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(34069, 'HP:0001609', 'Hoarse voice', 'XPO:0141770', 'abnormal urate homeostasis', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(34070, 'HP:0001609', 'Hoarse voice', 'XPO:0101468', 'abnormal stage I oocyte', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(34071, 'HP:0001609', 'Hoarse voice', 'XPO:0100307', 'abnormal blastomere', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(34072, 'HP:0001609', 'Hoarse voice', 'XPO:0100665', 'abnormal egg jelly', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34073, 'HP:0001609', 'Hoarse voice', 'XPO:0127101', 'abnormally localised portion of organism substance', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34074, 'HP:0001609', 'Hoarse voice', 'XPO:0101472', 'abnormal zygote cortex', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(34075, 'HP:0001609', 'Hoarse voice', 'XPO:0100791', 'abnormal multiciliated cell precursor', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(34076, 'HP:0001609', 'Hoarse voice', 'XPO:0100059', 'abnormal regenerating tail', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34077, 'HP:0001609', 'Hoarse voice', 'XPO:0101240', 'abnormal ciliated non-epidermal cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(34078, 'HP:0001609', 'Hoarse voice', 'XPO:0101333', 'abnormal barrier epithelial cell', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(34079, 'HP:0001609', 'Hoarse voice', 'XPO:0100742', 'abnormal musculoskeletal system', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34080, 'HP:0001609', 'Hoarse voice', 'XPO:0131469', 'abnormal heart process', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(34081, 'HP:0001609', 'Hoarse voice', 'XPO:0100902', 'abnormal spermatocyte', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(34082, 'HP:0001609', 'Hoarse voice', 'XPO:0141715', 'abnormal septum', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34083, 'HP:0001609', 'Hoarse voice', 'XPO:0100935', 'abnormal skeleton', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(34084, 'HP:0001609', 'Hoarse voice', 'XPO:0100093', 'abnormal simple squamous epithelium', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34085, 'HP:0001609', 'Hoarse voice', 'XPO:0100640', 'abnormal notochordal sheath', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(34086, 'HP:0001609', 'Hoarse voice', 'XPO:0100186', 'abnormal uveal tract', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34087, 'HP:0001609', 'Hoarse voice', 'XPO:0107258', 'abnormal anatomical axis', 0.5294117647058824, 1.706362323152461, 0.9504568842024205, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34088, 'HP:0001609', 'Hoarse voice', 'XPO:0101057', 'abnormal vegetal pole', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34089, 'HP:0001609', 'Hoarse voice', 'XPO:0100277', 'abnormal blastocoel', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34090, 'HP:0001609', 'Hoarse voice', 'XPO:0100081', 'abnormal anatomical entity in vitro', 0.5625, 1.706362323152461, 0.9797085315405084, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34091, 'HP:0001609', 'Hoarse voice', 'XPO:0141787', 'abnormal hormone metabolic process', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(34092, 'HP:0001609', 'Hoarse voice', 'XPO:0101480', 'abnormal stage V oocyte', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(34093, 'HP:0001609', 'Hoarse voice', 'XPO:0100612', 'abnormal unilaminar epithelium', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34094, 'HP:0001609', 'Hoarse voice', 'XPO:0101176', 'abnormal non-ciliated epithelial cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(34095, 'HP:0001609', 'Hoarse voice', 'XPO:0107276', 'abnormal dorsal region', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34096, 'HP:0001609', 'Hoarse voice', 'XPO:0101389', 'abnormal wedge region', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(34097, 'HP:0001609', 'Hoarse voice', 'XPO:0100916', 'abnormal principal cavity', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(34098, 'HP:0001609', 'Hoarse voice', 'XPO:0100900', 'abnormal angioblast', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(34099, 'HP:0001609', 'Hoarse voice', 'XPO:0100862', 'abnormal blastomere V1', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(34100, 'HP:0001609', 'Hoarse voice', 'XPO:0101501', 'abnormal parabrachial area', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(34101, 'HP:0001609', 'Hoarse voice', 'XPO:0100802', 'abnormal exocrine cell', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(34102, 'HP:0001609', 'Hoarse voice', 'XPO:0100151', 'abnormal primordium', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34103, 'HP:0001609', 'Hoarse voice', 'XPO:0107339', 'abnormal yolk platelet', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(34104, 'HP:0001609', 'Hoarse voice', 'XPO:0100991', 'abnormal iliac process primordium', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34105, 'HP:0001609', 'Hoarse voice', 'XPO:0100383', 'abnormal amputated fin', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34106, 'HP:0001609', 'Hoarse voice', 'XPO:0100025', 'abnormal oocyte', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(34107, 'HP:0001609', 'Hoarse voice', 'XPO:0100894', 'abnormal nucleus', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(34108, 'HP:0001609', 'Hoarse voice', 'XPO:0100218', 'abnormal epithelial cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(34109, 'HP:0001609', 'Hoarse voice', 'XPO:0107269', 'abnormal right side', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34110, 'HP:0001609', 'Hoarse voice', 'XPO:0100014', 'abnormal tissue', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34111, 'HP:0001609', 'Hoarse voice', 'XPO:0101269', 'abnormal mesodermal cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(34112, 'HP:0001609', 'Hoarse voice', 'XPO:0101083', 'abnormal T cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(34113, 'HP:0001609', 'Hoarse voice', 'XPO:0107311', 'abnormal apical junction complex', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(34114, 'HP:0001609', 'Hoarse voice', 'XPO:0100363', 'abnormal cardiovascular system', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34115, 'HP:0001609', 'Hoarse voice', 'XPO:0101589', 'abnormal blastocoel roof', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34116, 'HP:0001609', 'Hoarse voice', 'XPO:0100002', 'abnormal head', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(34117, 'HP:0001609', 'Hoarse voice', 'XPO:0100537', 'abnormal medium cavity', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(34118, 'HP:0001609', 'Hoarse voice', 'XPO:0101362', 'abnormal vegetal cortex', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(34119, 'HP:0001609', 'Hoarse voice', 'XPO:0141748', 'abnormal gas homeostasis', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(34120, 'HP:0001609', 'Hoarse voice', 'XPO:0100267', 'abnormal wound epidermis', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34121, 'HP:0001609', 'Hoarse voice', 'XPO:0101136', 'abnormal ooplasm', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(34122, 'HP:0001609', 'Hoarse voice', 'XPO:0101072', 'abnormal mitochondrial cloud', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(34123, 'HP:0001609', 'Hoarse voice', 'XPO:0101241', 'abnormal nucleate erythrocyte', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(34124, 'HP:0001609', 'Hoarse voice', 'XPO:0100296', 'abnormal tail region', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34125, 'HP:0001609', 'Hoarse voice', 'XPO:0100158', 'abnormal neuromere', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(34126, 'HP:0001609', 'Hoarse voice', 'XPO:0100339', 'abnormal circumblastoporal collar', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34127, 'HP:0001609', 'Hoarse voice', 'XPO:0100704', 'abnormal Merkel cell', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(34128, 'HP:0001609', 'Hoarse voice', 'XPO:0101533', 'abnormal simple cuboidal epithelium', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34129, 'HP:0001609', 'Hoarse voice', 'XPO:0100023', 'abnormal mesenchyme', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34130, 'HP:0001609', 'Hoarse voice', 'XPO:0100728', 'abnormal cell condensation', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34131, 'HP:0001609', 'Hoarse voice', 'XPO:0131677', 'abnormal actin filament', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(34132, 'HP:0001609', 'Hoarse voice', 'XPO:0100108', 'abnormal cell part', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(34133, 'HP:0001609', 'Hoarse voice', 'XPO:0107288', 'abnormal larval alimentary system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(34134, 'HP:0001609', 'Hoarse voice', 'XPO:0100627', 'abnormal pharyngeal region', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(34135, 'HP:0001609', 'Hoarse voice', 'XPO:0100890', 'abnormal pharyngeal cavity', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(34136, 'HP:0001609', 'Hoarse voice', 'XPO:0101326', 'abnormal cementoblast', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(34137, 'HP:0001609', 'Hoarse voice', 'XPO:0101264', 'abnormal mitotic spindle', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(34138, 'HP:0001609', 'Hoarse voice', 'XPO:0100289', 'abnormal chondroblast', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(34139, 'HP:0001609', 'Hoarse voice', 'XPO:0142056', 'abnormal main body axis', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34140, 'HP:0001609', 'Hoarse voice', 'XPO:0142057', 'abnormal desmosome', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(34141, 'HP:0001609', 'Hoarse voice', 'XPO:0100239', 'abnormal acellular anatomical structure', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34142, 'HP:0001609', 'Hoarse voice', 'XPO:0100251', 'abnormal proteinaceous extracellular matrix', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34143, 'HP:0001609', 'Hoarse voice', 'XPO:0100540', 'abnormal left lymph heart', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(34144, 'HP:0001609', 'Hoarse voice', 'XPO:0100503', 'abnormal blastomere D2', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(34145, 'HP:0001609', 'Hoarse voice', 'XPO:0101976', 'abnormal portion of organism substance morphology', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34146, 'HP:0001609', 'Hoarse voice', 'XPO:0100702', 'abnormal glial cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(34147, 'HP:0001609', 'Hoarse voice', 'XPO:0141791', 'abnormal primary metabolic process', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(34148, 'HP:0001609', 'Hoarse voice', 'XPO:0101378', 'abnormal blastomere D1', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(34149, 'HP:0001609', 'Hoarse voice', 'XPO:0100398', 'abnormal vegetal blastomere', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(34150, 'HP:0001609', 'Hoarse voice', 'XPO:0131745', 'abnormal axis elongation', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(34151, 'HP:0001609', 'Hoarse voice', 'XPO:0115473', 'abnormally delayed phase of Mullerian duct', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(34152, 'HP:0001609', 'Hoarse voice', 'XPO:0100146', 'abnormal primary germ layer', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34153, 'HP:0001609', 'Hoarse voice', 'XPO:0100691', 'abnormal keratin accumulating cell', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(34154, 'HP:0001609', 'Hoarse voice', 'XPO:0100553', 'abnormal laryngeal muscle primordium', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34155, 'HP:0001609', 'Hoarse voice', 'XPO:0141497', 'abnormal lymphoblast', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(34156, 'HP:0001609', 'Hoarse voice', 'XPO:0100196', 'abnormal neuron', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(34157, 'HP:0001609', 'Hoarse voice', 'XPO:0100422', 'abnormal notochord', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(34158, 'HP:0001609', 'Hoarse voice', 'XPO:0100285', 'abnormal progenitor cell', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(34159, 'HP:0001609', 'Hoarse voice', 'XPO:0101577', 'abnormal notochordal epithelium', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34160, 'HP:0001609', 'Hoarse voice', 'XPO:0141796', 'abnormal demethylation', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(34161, 'HP:0001609', 'Hoarse voice', 'XPO:0131725', 'abnormal phosphorylation of RNA polymerase II C-terminal domain', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(34162, 'HP:0001609', 'Hoarse voice', 'XPO:0141777', 'abnormal catabolic process', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(34163, 'HP:0001609', 'Hoarse voice', 'XPO:0100103', 'abnormal trunk', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34164, 'HP:0001609', 'Hoarse voice', 'XPO:0101224', 'abnormal dorsal involuting marginal zone', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34165, 'HP:0001609', 'Hoarse voice', 'XPO:0100120', 'abnormal genital system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(34166, 'HP:0001609', 'Hoarse voice', 'XPO:0100009', 'abnormal multi-tissue structure', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34167, 'HP:0001609', 'Hoarse voice', 'XPO:00000000', 'Xenopus phenotype', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(34168, 'HP:0001609', 'Hoarse voice', 'XPO:0100551', 'abnormal oocyte cortex', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(34169, 'HP:0001609', 'Hoarse voice', 'XPO:0142054', 'abnormal digestive tract', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(34170, 'HP:0001609', 'Hoarse voice', 'XPO:0141904', 'abnormal glucosamine metabolic process', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(34171, 'HP:0001609', 'Hoarse voice', 'XPO:0141775', 'abnormal nitrogen compound metabolic process', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(34172, 'HP:0001609', 'Hoarse voice', 'XPO:0141499', 'abnormal tadpole', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34173, 'HP:0001609', 'Hoarse voice', 'XPO:0100816', 'abnormal blastocoel anlage', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34174, 'HP:0001609', 'Hoarse voice', 'XPO:0101543', 'abnormal external gill', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(34175, 'HP:0001609', 'Hoarse voice', 'XPO:0100069', 'abnormal urinary system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(34176, 'HP:0001609', 'Hoarse voice', 'XPO:0131691', 'abnormal molecular function', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(34177, 'HP:0001609', 'Hoarse voice', 'XPO:0100062', 'abnormal anatomical space', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34178, 'HP:0001609', 'Hoarse voice', 'XPO:0100610', 'abnormal appendage', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34179, 'HP:0001609', 'Hoarse voice', 'XPO:0100392', 'abnormal cilium', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(34180, 'HP:0001609', 'Hoarse voice', 'XPO:0116494', 'absent biological process', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(34181, 'HP:0001609', 'Hoarse voice', 'XPO:0100701', 'abnormal microglial cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(34182, 'HP:0001609', 'Hoarse voice', 'XPO:0141792', 'abnormal small molecule metabolic process', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(34183, 'HP:0001609', 'Hoarse voice', 'XPO:0100585', 'abnormal elastica externa', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(34184, 'HP:0001609', 'Hoarse voice', 'XPO:0141783', 'abnormal collagen metabolic process', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(34185, 'HP:0001609', 'Hoarse voice', 'XPO:0100402', 'abnormal zeugopod', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(34186, 'HP:0001609', 'Hoarse voice', 'XPO:0107263', 'abnormal anatomical side', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34187, 'HP:0001609', 'Hoarse voice', 'XPO:0100486', 'abnormal oral evagination', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(34188, 'HP:0001609', 'Hoarse voice', 'XPO:0107259', 'abnormal animal-vegetal axis', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34189, 'HP:0001609', 'Hoarse voice', 'XPO:0131669', 'abnormal Roux spot', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(34190, 'HP:0001609', 'Hoarse voice', 'XPO:0100872', 'abnormal neuroendocrine cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(34191, 'HP:0001609', 'Hoarse voice', 'XPO:0100207', 'abnormal blastema', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34192, 'HP:0001609', 'Hoarse voice', 'XPO:0100265', 'abnormal sensory epithelial cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(34193, 'HP:0001609', 'Hoarse voice', 'XPO:0100864', 'abnormal dorsolateral ascending neuron', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(34194, 'HP:0001609', 'Hoarse voice', 'XPO:0100735', 'abnormal hindgut', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(34195, 'HP:0001609', 'Hoarse voice', 'XPO:0100386', 'abnormal limb', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(34196, 'HP:0001609', 'Hoarse voice', 'XPO:0101023', 'abnormal ultimobranchial body', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(34197, 'HP:0001609', 'Hoarse voice', 'XPO:0100823', 'abnormal blood', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(34198, 'HP:0001609', 'Hoarse voice', 'XPO:0116434', 'abnormal biological process', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(34199, 'HP:0001609', 'Hoarse voice', 'XPO:0100523', 'abnormal midgut', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(34200, 'HP:0001609', 'Hoarse voice', 'XPO:0126318', 'abnormally localised cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(34201, 'HP:0001609', 'Hoarse voice', 'XPO:0100969', 'abnormal disaggregated/reaggregated ectoderm treated with activin', 0.5294117647058824, 1.706362323152461, 0.9504568842024205, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34202, 'HP:0001609', 'Hoarse voice', 'XPO:0100225', 'abnormal endocrine system', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(34203, 'HP:0001609', 'Hoarse voice', 'XPO:0115758', 'abnormally decreased mobility of melanoblast', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(34204, 'HP:0001609', 'Hoarse voice', 'XPO:0100393', 'abnormal involuting marginal zone', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34205, 'HP:0001609', 'Hoarse voice', 'XPO:0141786', 'abnormal pigment metabolic process', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(34206, 'HP:0001609', 'Hoarse voice', 'XPO:0101228', 'abnormal mesenchymal stem cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(34207, 'HP:0001609', 'Hoarse voice', 'XPO:0101553', 'abnormal dental epithelium', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34208, 'HP:0001609', 'Hoarse voice', 'XPO:0100750', 'abnormal regenerating fin', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34209, 'HP:0001609', 'Hoarse voice', 'XPO:0107278', 'abnormal medial region', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34210, 'HP:0001609', 'Hoarse voice', 'XPO:0142052', 'abnormal nasal region', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(34211, 'HP:0001609', 'Hoarse voice', 'XPO:0101467', 'abnormal alkali secreting cell', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(34212, 'HP:0001609', 'Hoarse voice', 'XPO:0100999', 'abnormal serous membrane', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34213, 'HP:0001609', 'Hoarse voice', 'XPO:0100202', 'abnormal embryo', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34214, 'HP:0001609', 'Hoarse voice', 'XPO:0100687', 'abnormal periotic region', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(34215, 'HP:0001609', 'Hoarse voice', 'XPO:0100827', 'abnormal atypical epithelium', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34216, 'HP:0001609', 'Hoarse voice', 'XPO:0101096', 'abnormal tendon', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(34217, 'HP:0001609', 'Hoarse voice', 'XPO:0126624', 'abnormally localised anatomical line', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34218, 'HP:0001609', 'Hoarse voice', 'XPO:0100799', 'abnormal genital ridge', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(34219, 'HP:0001609', 'Hoarse voice', 'XPO:0100308', 'abnormal early embryonic cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(34220, 'HP:0001609', 'Hoarse voice', 'XPO:0100372', 'abnormal hematological system', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(34221, 'HP:0001609', 'Hoarse voice', 'XPO:0100754', 'abnormal electrically active cell', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(34222, 'HP:0001609', 'Hoarse voice', 'XPO:0100688', 'abnormal adipose tissue', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(34223, 'HP:0001609', 'Hoarse voice', 'XPO:0100587', 'abnormal vestibuloauditory system', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(34224, 'HP:0001609', 'Hoarse voice', 'XPO:0101149', 'abnormal amputated limb', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34225, 'HP:0001609', 'Hoarse voice', 'XPO:0100511', 'abnormal stylopod', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(34226, 'HP:0001609', 'Hoarse voice', 'XPO:0100376', 'abnormal animal pole', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34227, 'HP:0001609', 'Hoarse voice', 'XPO:0101402', 'abnormal oropharyngeal papilla', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(34228, 'HP:0001609', 'Hoarse voice', 'XPO:0101498', 'abnormal stage II oocyte', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(34229, 'HP:0001609', 'Hoarse voice', 'XPO:0100203', 'abnormal endocrine cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(34230, 'HP:0001609', 'Hoarse voice', 'XPO:0133388', 'absent insulin receptor signaling pathway', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(34231, 'HP:0001609', 'Hoarse voice', 'XPO:0101519', 'abnormal hypobranchial placode', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34232, 'HP:0001609', 'Hoarse voice', 'XPO:0100384', 'abnormal amputated tissue', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34233, 'HP:0001609', 'Hoarse voice', 'XPO:0101406', 'abnormal cleavage furrow', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34234, 'HP:0001609', 'Hoarse voice', 'XPO:0101713', 'abnormal anatomical entity in vitro morphology', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34235, 'HP:0001609', 'Hoarse voice', 'XPO:0100192', 'abnormal epithelium', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34236, 'HP:0001609', 'Hoarse voice', 'XPO:0101409', 'abnormal perivitelline space', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(34237, 'HP:0001609', 'Hoarse voice', 'XPO:0101518', 'abnormal B cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(34238, 'HP:0001609', 'Hoarse voice', 'XPO:0131723', 'abnormal pathway-restricted SMAD protein phosphorylation', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(34239, 'HP:0001609', 'Hoarse voice', 'XPO:0100344', 'abnormal portion of organism substance', 0.5625, 1.706362323152461, 0.9797085315405084, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34240, 'HP:0001609', 'Hoarse voice', 'XPO:0101575', 'abnormal vitelline membrane', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(34241, 'HP:0001609', 'Hoarse voice', 'XPO:0100667', 'abnormal vegetal yolk mass', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34242, 'HP:0001609', 'Hoarse voice', 'XPO:0100976', 'abnormal multiciliated cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(34243, 'HP:0001609', 'Hoarse voice', 'XPO:0128000', 'absent behavior', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(34244, 'HP:0001609', 'Hoarse voice', 'XPO:0125007', 'absent anatomical line', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34245, 'HP:0001609', 'Hoarse voice', 'XPO:0115574', 'abnormal variability of size of hindlimb', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(34246, 'HP:0001609', 'Hoarse voice', 'XPO:0116091', 'abnormally increased variability of size of cell in endoderm', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(34247, 'HP:0001609', 'Hoarse voice', 'XPO:0141771', 'abnormal urea homeostasis', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(34248, 'HP:0001609', 'Hoarse voice', 'XPO:0100912', 'abnormal trabecula', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34249, 'HP:0001609', 'Hoarse voice', 'XPO:0107272', 'abnormal axial region', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34250, 'HP:0001609', 'Hoarse voice', 'XPO:0100533', 'abnormal melanoblast', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(34251, 'HP:0001609', 'Hoarse voice', 'XPO:0101448', 'abnormal myelin accumulating cell', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(34252, 'HP:0001609', 'Hoarse voice', 'XPO:0100444', 'abnormal cement gland', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34253, 'HP:0001609', 'Hoarse voice', 'XPO:0100989', 'abnormal right blastomere', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(34254, 'HP:0001609', 'Hoarse voice', 'XPO:0100249', 'abnormal avascular GAG-rich matrix', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34255, 'HP:0001609', 'Hoarse voice', 'XPO:0100599', 'abnormal adult immune system', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(34256, 'HP:0001609', 'Hoarse voice', 'XPO:0100070', 'abnormal anatomical system', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34257, 'HP:0001609', 'Hoarse voice', 'XPO:0115505', 'dead whole organism', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34258, 'HP:0001609', 'Hoarse voice', 'XPO:0100574', 'abnormal gastrula cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(34259, 'HP:0001609', 'Hoarse voice', 'XPO:0100255', 'abnormal pelvic appendage', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34260, 'HP:0001609', 'Hoarse voice', 'XPO:0101513', 'abnormal basal body', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(34261, 'HP:0001609', 'Hoarse voice', 'XPO:0100437', 'abnormal proepicardium', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(34262, 'HP:0001609', 'Hoarse voice', 'XPO:0100858', 'abnormal presumptive midbrain-hindbrain boundary', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(34263, 'HP:0001609', 'Hoarse voice', 'XPO:0107284', 'abnormal migrating myoblast', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(34264, 'HP:0001609', 'Hoarse voice', 'XPO:0141600', 'absent metamorphosis', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(34265, 'HP:0001609', 'Hoarse voice', 'XPO:0141754', 'abnormal homeostatic process', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(34266, 'HP:0001609', 'Hoarse voice', 'XPO:0101396', 'abnormal apical epithelial cap', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34267, 'HP:0001609', 'Hoarse voice', 'XPO:0101560', 'abnormal compound organ component', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34268, 'HP:0001609', 'Hoarse voice', 'XPO:0131730', 'abnormal regulation of protein folding', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(34269, 'HP:0001609', 'Hoarse voice', 'XPO:0101221', 'abnormal larval immune system', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(34270, 'HP:0001609', 'Hoarse voice', 'XPO:0100545', 'abnormal male organism', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34271, 'HP:0001609', 'Hoarse voice', 'XPO:0101461', 'abnormal sperm entry point', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(34272, 'HP:0001609', 'Hoarse voice', 'XPO:0100477', 'abnormal pericyte', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(34273, 'HP:0001609', 'Hoarse voice', 'XPO:0107266', 'abnormal dorsal side', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34274, 'HP:0001609', 'Hoarse voice', 'XPO:0100028', 'abnormal anatomical cluster', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34275, 'HP:0001609', 'Hoarse voice', 'XPO:0100465', 'abnormal skeletal system', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(34276, 'HP:0001609', 'Hoarse voice', 'XPO:0100429', 'abnormal spermatid', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(34277, 'HP:0001609', 'Hoarse voice', 'XPO:0101573', 'abnormal peripheral vegetal yolk mass', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34278, 'HP:0001609', 'Hoarse voice', 'XPO:0131687', 'abnormal astral microtubule', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(34279, 'HP:0001609', 'Hoarse voice', 'XPO:0141841', 'abnormality of whole organism mass', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(34280, 'HP:0001609', 'Hoarse voice', 'XPO:0101347', 'abnormal hindlimb region', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34281, 'HP:0001609', 'Hoarse voice', 'XPO:0101638', 'abnormal anatomical structure morphology', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34282, 'HP:0001609', 'Hoarse voice', 'XPO:0115509', 'abnormally semi-viable whole organism', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34283, 'HP:0001609', 'Hoarse voice', 'XPO:0101411', 'abnormal marginal zone (sensu neural)', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34284, 'HP:0001609', 'Hoarse voice', 'XPO:0100268', 'abnormal circulatory system', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34285, 'HP:0001609', 'Hoarse voice', 'XPO:0101403', 'abnormal basal lamina', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34286, 'HP:0001609', 'Hoarse voice', 'XPO:0100004', 'abnormal cell', 0.55, 1.8210412618256888, 1.0007860380741376, 'HP:0000118', 'Phenotypic abnormality'),
(34287, 'HP:0001609', 'Hoarse voice', 'XPO:0100258', 'abnormal organ part', 0.5294117647058824, 1.706362323152461, 0.9504568842024205, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34288, 'HP:0001609', 'Hoarse voice', 'XPO:0141264', 'abnormal schooling behavior', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(34289, 'HP:0001609', 'Hoarse voice', 'XPO:0100481', 'abnormal anatomical line', 0.5625, 1.706362323152461, 0.9797085315405084, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34290, 'HP:0001609', 'Hoarse voice', 'XPO:0100664', 'abnormal periocular region', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(34291, 'HP:0001609', 'Hoarse voice', 'XPO:0100242', 'abnormal right lymph heart', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(34292, 'HP:0001609', 'Hoarse voice', 'XPO:0141860', 'abnormal malate-aspartate shuttle', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(34293, 'HP:0001609', 'Hoarse voice', 'XPO:0141266', 'abnormal surface breathing', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(34294, 'HP:0001609', 'Hoarse voice', 'XPO:0101109', 'abnormal egg cell-free extract', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34295, 'HP:0001609', 'Hoarse voice', 'XPO:0141795', 'abnormal glycosylation', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(34296, 'HP:0001609', 'Hoarse voice', 'XPO:0100403', 'abnormal forelimb', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(34297, 'HP:0001609', 'Hoarse voice', 'XPO:0100501', 'abnormal urogenital system', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(34298, 'HP:0001609', 'Hoarse voice', 'XPO:0101311', 'abnormal bottle cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(34299, 'HP:0001609', 'Hoarse voice', 'XPO:0100309', 'abnormal vegetal hemisphere', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34300, 'HP:0001609', 'Hoarse voice', 'XPO:0141907', 'abnormal putrescine metabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(34301, 'HP:0001609', 'Hoarse voice', 'XPO:0100205', 'abnormal limb segment', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(34302, 'HP:0001609', 'Hoarse voice', 'XPO:0126321', 'abnormally localised anatomical structure', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34303, 'HP:0001609', 'Hoarse voice', 'XPO:0100915', 'abnormal dermal system', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34304, 'HP:0001609', 'Hoarse voice', 'XPO:0100546', 'abnormal whole organism', 0.5294117647058824, 1.706362323152461, 0.9504568842024205, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34305, 'HP:0001609', 'Hoarse voice', 'XPO:0107271', 'abnormal apical region', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34306, 'HP:0001609', 'Hoarse voice', 'XPO:0101500', 'abnormal endodermal cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(34307, 'HP:0001609', 'Hoarse voice', 'XPO:0101092', 'abnormal dorso-lateral marginal zone', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34308, 'HP:0001609', 'Hoarse voice', 'XPO:0131685', 'abnormal cortical actin cytoskeleton', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(34309, 'HP:0001609', 'Hoarse voice', 'XPO:0100653', 'abnormal myoblast', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(34310, 'HP:0001609', 'Hoarse voice', 'XPO:0100449', 'abnormal lymphocyte', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(34311, 'HP:0001609', 'Hoarse voice', 'XPO:0100423', 'abnormal process', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34312, 'HP:0001609', 'Hoarse voice', 'XPO:0101174', 'abnormal articular system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(34313, 'HP:0001609', 'Hoarse voice', 'XPO:0101263', 'abnormal blastocoel floor', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34314, 'HP:0001609', 'Hoarse voice', 'XPO:0100913', 'abnormal Brachets cleft', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34315, 'HP:0001609', 'Hoarse voice', 'XPO:0115391', 'abnormally undifferentiated alimentary system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(34316, 'HP:0001609', 'Hoarse voice', 'XPO:0107260', 'abnormal anterior-posterior axis', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34317, 'HP:0001609', 'Hoarse voice', 'XPO:0101435', 'abnormal paracrine cell', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(34318, 'HP:0001609', 'Hoarse voice', 'XPO:0100377', 'abnormal connective tissue', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(34319, 'HP:0001609', 'Hoarse voice', 'XPO:0100843', 'abnormal fasciculated network of fibrils', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(34320, 'HP:0001609', 'Hoarse voice', 'XPO:0100458', 'abnormal autopod', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(34321, 'HP:0001609', 'Hoarse voice', 'XPO:0131729', 'abnormal regulation of growth rate', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(34322, 'HP:0001609', 'Hoarse voice', 'XPO:0100417', 'abnormal dense regular connective tissue', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(34323, 'HP:0001609', 'Hoarse voice', 'XPO:0100638', 'abnormal polar body', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(34324, 'HP:0001609', 'Hoarse voice', 'XPO:0141743', 'abnormal chemical homeostasis within a tissue', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(34325, 'HP:0001609', 'Hoarse voice', 'XPO:0107253', 'abnormal enteric nervous system', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(34326, 'HP:0001609', 'Hoarse voice', 'XPO:0100003', 'abnormal organism subdivision', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34327, 'HP:0001609', 'Hoarse voice', 'XPO:0100531', 'abnormal proliferative region', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34328, 'HP:0001609', 'Hoarse voice', 'XPO:0141781', 'abnormal secondary metabolic process', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(34329, 'HP:0001609', 'Hoarse voice', 'XPO:0101366', 'abnormal morula cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(34330, 'HP:0001609', 'Hoarse voice', 'XPO:0100006', 'abnormal anatomical structure', 0.5625, 1.706362323152461, 0.9797085315405084, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34331, 'HP:0001609', 'Hoarse voice', 'XPO:0100172', 'abnormal stem cell', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(34332, 'HP:0001609', 'Hoarse voice', 'XPO:0101297', 'abnormal barrier cell', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(34333, 'HP:0001609', 'Hoarse voice', 'XPO:0100232', 'abnormal lymphatic system', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(34334, 'HP:0001609', 'Hoarse voice', 'XPO:0100187', 'abnormal regenerating limb', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34335, 'HP:0001609', 'Hoarse voice', 'XPO:0100067', 'abnormal animal hemisphere', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34336, 'HP:0001609', 'Hoarse voice', 'XPO:0115512', 'abnormally semi-erect whole organism', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34337, 'HP:0001609', 'Hoarse voice', 'XPO:0101547', 'abnormal lampbrush chromosome', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(34338, 'HP:0001609', 'Hoarse voice', 'XPO:0141778', 'abnormal biosynthetic process', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(34339, 'HP:0001609', 'Hoarse voice', 'XPO:0100231', 'abnormal compound organ', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34340, 'HP:0001609', 'Hoarse voice', 'XPO:0101460', 'abnormal fibrocellular pad', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34341, 'HP:0001609', 'Hoarse voice', 'XPO:0100228', 'abnormal skeletal subdivision', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(34342, 'HP:0001609', 'Hoarse voice', 'XPO:0141809', 'abnormal catalytic activity', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(34343, 'HP:0001609', 'Hoarse voice', 'XPO:0100515', 'abnormal somatic stem cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(34344, 'HP:0001609', 'Hoarse voice', 'XPO:0101740', 'abnormal cell part morphology', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(34345, 'HP:0001609', 'Hoarse voice', 'XPO:0100152', 'abnormal alimentary system', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(34346, 'HP:0001609', 'Hoarse voice', 'XPO:0141263', 'abnormal visually guided collision avoidance behavior', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(34347, 'HP:0001609', 'Hoarse voice', 'XPO:0101157', 'abnormal female organism', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34348, 'HP:0001609', 'Hoarse voice', 'XPO:0107264', 'abnormal anterior side', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34349, 'HP:0001609', 'Hoarse voice', 'XPO:0101078', 'abnormal mucous gland', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34350, 'HP:0001609', 'Hoarse voice', 'XPO:0100010', 'abnormal multicellular anatomical structure', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34351, 'HP:0001609', 'Hoarse voice', 'XPO:0131666', 'abnormal adherens junction', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(34352, 'HP:0001609', 'Hoarse voice', 'XPO:0100760', 'abnormal Stirnorgan', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(34353, 'HP:0001609', 'Hoarse voice', 'XPO:0101200', 'abnormal joint region', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34354, 'HP:0001609', 'Hoarse voice', 'XPO:0101099', 'abnormal ventro-lateral marginal zone', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34355, 'HP:0001609', 'Hoarse voice', 'XPO:0133403', 'abnormal developmental process', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(34356, 'HP:0001609', 'Hoarse voice', 'XPO:0100164', 'abnormal neural nucleus', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(34357, 'HP:0001609', 'Hoarse voice', 'XPO:0100867', 'abnormal apical mesenchyme', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34358, 'HP:0001609', 'Hoarse voice', 'XPO:0100416', 'abnormal ligament', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(34359, 'HP:0001609', 'Hoarse voice', 'XPO:0101463', 'abnormal right-ventral blastomere', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(34360, 'HP:0001609', 'Hoarse voice', 'XPO:0100433', 'abnormal pectoral appendage', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34361, 'HP:0001609', 'Hoarse voice', 'XPO:0100293', 'abnormal duct', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34362, 'HP:0001609', 'Hoarse voice', 'XPO:0101497', 'abnormal ciliary axoneme', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(34363, 'HP:0001609', 'Hoarse voice', 'XPO:0142051', 'abnormal cerebrospinal fluid', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(34364, 'HP:0001609', 'Hoarse voice', 'XPO:0107262', 'abnormal left-right axis', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34365, 'HP:0001609', 'Hoarse voice', 'XPO:0115566', 'abnormal variability of size of forelimb', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(34366, 'HP:0001609', 'Hoarse voice', 'XPO:0101283', 'abnormal left-ventral blastomere', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(34367, 'HP:0001609', 'Hoarse voice', 'XPO:0101187', 'abnormal dorsolateral commissural neuron', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(34368, 'HP:0001609', 'Hoarse voice', 'XPO:0100917', 'abnormal stage III oocyte', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(34369, 'HP:0001609', 'Hoarse voice', 'XPO:0101074', 'abnormal germinal vesicle', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(34370, 'HP:0001609', 'Hoarse voice', 'XPO:0100887', 'abnormal right-dorsal blastomere', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(34371, 'HP:0001609', 'Hoarse voice', 'XPO:0100642', 'abnormal gustatory system', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(34372, 'HP:0001609', 'Hoarse voice', 'XPO:0141738', 'abnormal carbon dioxide homeostasis', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(34373, 'HP:0001609', 'Hoarse voice', 'XPO:0100626', 'abnormal primordial germ cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(34374, 'HP:0001609', 'Hoarse voice', 'XPO:0100974', 'abnormal cardiac mesoderm', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34375, 'HP:0001609', 'Hoarse voice', 'XPO:0100852', 'abnormal interdigital region', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(34376, 'HP:0001609', 'Hoarse voice', 'XPO:0100274', 'abnormal sensory system', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(34377, 'HP:0001609', 'Hoarse voice', 'XPO:0101450', 'abnormal myeloid cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(34378, 'HP:0001609', 'Hoarse voice', 'XPO:0101587', 'abnormal hemangioblast', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(34379, 'HP:0001609', 'Hoarse voice', 'XPO:0141718', 'abnormal posterior notochord', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(34380, 'HP:0001609', 'Hoarse voice', 'XPO:0101168', 'abnormal circulating cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(34381, 'HP:0001609', 'Hoarse voice', 'XPO:0100026', 'abnormal germ cell', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(34382, 'HP:0001609', 'Hoarse voice', 'XPO:0115362', 'abnormally decreased adhesivity of prechordal plate', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34383, 'HP:0001609', 'Hoarse voice', 'XPO:0101349', 'abnormal trunk region', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34384, 'HP:0001609', 'Hoarse voice', 'XPO:0101107', 'abnormal erythroid cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(34385, 'HP:0001609', 'Hoarse voice', 'XPO:0141784', 'abnormal cellular hormone metabolic process', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(34386, 'HP:0001609', 'Hoarse voice', 'XPO:0100573', 'abnormal extraembryonic structure', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34387, 'HP:0001609', 'Hoarse voice', 'XPO:0141776', 'abnormal metabolic process', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(34388, 'HP:0001609', 'Hoarse voice', 'XPO:0101212', 'abnormal glomeral mesenchyme', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(34389, 'HP:0001609', 'Hoarse voice', 'XPO:0100261', 'abnormal multilaminar epithelium', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34390, 'HP:0001609', 'Hoarse voice', 'XPO:0141745', 'abnormal creatinine homeostasis', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(34391, 'HP:0001609', 'Hoarse voice', 'XPO:0141772', 'abnormal water homeostasis', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(34392, 'HP:0001609', 'Hoarse voice', 'XPO:0101377', 'abnormal manicotto glandulare', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(34393, 'HP:0001609', 'Hoarse voice', 'XPO:0100856', 'abnormal simple organ', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34394, 'HP:0001609', 'Hoarse voice', 'XPO:0101004', 'abnormal acid secreting cell', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(34395, 'HP:0001609', 'Hoarse voice', 'XPO:0102113', 'abnormal anatomical line morphology', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34396, 'HP:0001609', 'Hoarse voice', 'XPO:0100616', 'abnormal ventral blood island', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(34397, 'HP:0001609', 'Hoarse voice', 'XPO:0107285', 'abnormal flexural organ', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(34398, 'HP:0001609', 'Hoarse voice', 'XPO:0100557', 'abnormal prime meridian', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34399, 'HP:0001609', 'Hoarse voice', 'XPO:0141790', 'abnormal cellular metabolic process', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(34400, 'HP:0001609', 'Hoarse voice', 'XPO:0101503', 'abnormal organ cortex', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34401, 'HP:0001609', 'Hoarse voice', 'XPO:0100786', 'abnormal presumptive axial mesoderm', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34402, 'HP:0001609', 'Hoarse voice', 'XPO:0100807', 'abnormal matrix-based tissue', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34403, 'HP:0001609', 'Hoarse voice', 'XPO:0101113', 'abnormal stage IV oocyte', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(34404, 'HP:0001609', 'Hoarse voice', 'XPO:0100521', 'abnormal animal blastomere', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(34405, 'HP:0001609', 'Hoarse voice', 'XPO:0101040', 'abnormal axial mesoderm', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34406, 'HP:0001609', 'Hoarse voice', 'XPO:0141794', 'abnormal prosthetic group metabolic process', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(34407, 'HP:0001609', 'Hoarse voice', 'XPO:0100156', 'abnormal foregut', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(34408, 'HP:0001609', 'Hoarse voice', 'XPO:0100745', 'abnormal anterior lymph sac', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(34409, 'HP:0001609', 'Hoarse voice', 'XPO:0141265', 'abnormal escape behavior', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(34410, 'HP:0001609', 'Hoarse voice', 'XPO:0141782', 'abnormal methylation', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(34411, 'HP:0001609', 'Hoarse voice', 'XPO:0131667', 'abnormal actin cytoskeleton', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(34412, 'HP:0001609', 'Hoarse voice', 'XPO:0107261', 'abnormal dorsal-ventral axis', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34413, 'HP:0001609', 'Hoarse voice', 'XPO:0100860', 'abnormal parathyroid', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(34414, 'HP:0001609', 'Hoarse voice', 'XPO:0107267', 'abnormal ventral side', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34415, 'HP:0001609', 'Hoarse voice', 'XPO:0100133', 'abnormal solid compound organ', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34416, 'HP:0001609', 'Hoarse voice', 'XPO:0100643', 'abnormal thoracic region', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34417, 'HP:0001609', 'Hoarse voice', 'XPO:0100722', 'abnormal barbel', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34418, 'HP:0001609', 'Hoarse voice', 'XPO:0107270', 'abnormal proximal-distal axis', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34419, 'HP:0001609', 'Hoarse voice', 'XPO:0100907', 'abnormal cytoplasm', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(34420, 'HP:0001609', 'Hoarse voice', 'XPO:0100727', 'abnormal odontogenic papilla', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(34421, 'HP:0001609', 'Hoarse voice', 'XPO:0141315', 'abnormal anatomical region', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34422, 'HP:0001609', 'Hoarse voice', 'XPO:0100427', 'abnormal olfactory system', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(34423, 'HP:0001609', 'Hoarse voice', 'XPO:0141892', 'abnormal inositol metabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(34424, 'HP:0001609', 'Hoarse voice', 'XPO:0100547', 'abnormal blastomere V2', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(34425, 'HP:0001609', 'Hoarse voice', 'XPO:0100800', 'abnormal ventral marginal zone', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34426, 'HP:0001609', 'Hoarse voice', 'XPO:0101098', 'abnormal mineralized extracellular matrix', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34427, 'HP:0001609', 'Hoarse voice', 'XPO:0100337', 'abnormal zygote', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(34428, 'HP:0001609', 'Hoarse voice', 'XPO:0100842', 'abnormal left-dorsal blastomere', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(34429, 'HP:0001609', 'Hoarse voice', 'XPO:0141797', 'abnormal hydrogen metabolic process', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(34430, 'HP:0001609', 'Hoarse voice', 'XPO:0100176', 'abnormal stage VI oocyte', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(34431, 'HP:0001609', 'Hoarse voice', 'XPO:0101162', 'abnormal stromal cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(34432, 'HP:0001609', 'Hoarse voice', 'XPO:0101535', 'abnormal absorptive cell', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(34433, 'HP:0001609', 'Hoarse voice', 'XPO:0115508', 'abnormally peramorphic growth of whole organism', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34434, 'HP:0001609', 'Hoarse voice', 'XPO:0101424', 'abnormal coelomic epithelium', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34435, 'HP:0001609', 'Hoarse voice', 'XPO:0100956', 'abnormal centrosome', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(34436, 'HP:0001609', 'Hoarse voice', 'XPO:0101141', 'abnormal Keller explant', 0.5294117647058824, 1.706362323152461, 0.9504568842024205, 'UPHENO:0002536', 'abnormal anatomical entity'),
(34437, 'HP:0001609', 'Hoarse voice', 'XPO:0131675', 'abnormal spindle microtubule', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(34438, 'HP:0001609', 'Hoarse voice', 'XPO:0100415', 'abnormal secretory epithelial cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(34439, 'HP:0001609', 'Hoarse voice', 'XPO:0100175', 'abnormal migrating neuroblast', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(34440, 'HP:0001609', 'Hoarse voice', 'XPO:0101061', 'abnormal plasma membrane', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(34441, 'HP:0001609', 'Hoarse voice', 'XPO:0100674', 'abnormal secondary oogonium', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(34442, 'HP:0001609', 'Hoarse voice', 'XPO:0100378', 'abnormal perichondrium', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
