(629038, 'HP:0034929', 'Reduced hepatic cystathionine gamma-lyase activity', 'XPO:0128000', 'absent behavior', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(629039, 'HP:0034929', 'Reduced hepatic cystathionine gamma-lyase activity', 'XPO:0101535', 'abnormal absorptive cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(629040, 'HP:0034929', 'Reduced hepatic cystathionine gamma-lyase activity', 'XPO:0141781', 'abnormal secondary metabolic process', 0.5238095238095238, 4.758907843651163, 1.5788480773767701, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(629041, 'HP:0034929', 'Reduced hepatic cystathionine gamma-lyase activity', 'XPO:0100477', 'abnormal pericyte', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(629042, 'HP:0034929', 'Reduced hepatic cystathionine gamma-lyase activity', 'XPO:0141792', 'abnormal small molecule metabolic process', 0.5238095238095238, 4.758907843651163, 1.5788480773767701, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(629043, 'HP:0034929', 'Reduced hepatic cystathionine gamma-lyase activity', 'XPO:0133403', 'abnormal developmental process', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(629044, 'HP:0034929', 'Reduced hepatic cystathionine gamma-lyase activity', 'XPO:0141767', 'abnormal temperature homeostasis', 0.44, 4.758907843651163, 1.447038165082909, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(629045, 'HP:0034929', 'Reduced hepatic cystathionine gamma-lyase activity', 'XPO:0141900', 'abnormal mannose metabolic process', 0.4230769230769231, 4.758907843651163, 1.418937661667548, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(629046, 'HP:0034929', 'Reduced hepatic cystathionine gamma-lyase activity', 'XPO:0141770', 'abnormal urate homeostasis', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(629047, 'HP:0034929', 'Reduced hepatic cystathionine gamma-lyase activity', 'XPO:0101241', 'abnormal nucleate erythrocyte', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(629048, 'HP:0034929', 'Reduced hepatic cystathionine gamma-lyase activity', 'XPO:0101240', 'abnormal ciliated non-epidermal cell', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(629049, 'HP:0034929', 'Reduced hepatic cystathionine gamma-lyase activity', 'XPO:0100574', 'abnormal gastrula cell', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(629050, 'HP:0034929', 'Reduced hepatic cystathionine gamma-lyase activity', 'XPO:0101513', 'abnormal basal body', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(629051, 'HP:0034929', 'Reduced hepatic cystathionine gamma-lyase activity', 'XPO:0107262', 'abnormal left-right axis', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(629052, 'HP:0034929', 'Reduced hepatic cystathionine gamma-lyase activity', 'XPO:0101141', 'abnormal Keller explant', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(629053, 'HP:0034929', 'Reduced hepatic cystathionine gamma-lyase activity', 'XPO:0101333', 'abnormal barrier epithelial cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(629054, 'HP:0034929', 'Reduced hepatic cystathionine gamma-lyase activity', 'XPO:0100899', 'abnormal secondary spermatogonium', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(629055, 'HP:0034929', 'Reduced hepatic cystathionine gamma-lyase activity', 'XPO:0116494', 'absent biological process', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(629056, 'HP:0034929', 'Reduced hepatic cystathionine gamma-lyase activity', 'XPO:0100026', 'abnormal germ cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(629057, 'HP:0034929', 'Reduced hepatic cystathionine gamma-lyase activity', 'XPO:0100437', 'abnormal proepicardium', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(629058, 'HP:0034929', 'Reduced hepatic cystathionine gamma-lyase activity', 'XPO:0131677', 'abnormal actin filament', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(629059, 'HP:0034929', 'Reduced hepatic cystathionine gamma-lyase activity', 'XPO:0100754', 'abnormal electrically active cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(629060, 'HP:0034929', 'Reduced hepatic cystathionine gamma-lyase activity', 'XPO:0100062', 'abnormal anatomical space', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(629061, 'HP:0034929', 'Reduced hepatic cystathionine gamma-lyase activity', 'XPO:0100638', 'abnormal polar body', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(629062, 'HP:0034929', 'Reduced hepatic cystathionine gamma-lyase activity', 'XPO:0100545', 'abnormal male organism', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(629063, 'HP:0034929', 'Reduced hepatic cystathionine gamma-lyase activity', 'XPO:0131667', 'abnormal actin cytoskeleton', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(629064, 'HP:0034929', 'Reduced hepatic cystathionine gamma-lyase activity', 'XPO:0131685', 'abnormal cortical actin cytoskeleton', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(629065, 'HP:0034929', 'Reduced hepatic cystathionine gamma-lyase activity', 'XPO:0141499', 'abnormal tadpole', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(629066, 'HP:0034929', 'Reduced hepatic cystathionine gamma-lyase activity', 'XPO:0100429', 'abnormal spermatid', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(629067, 'HP:0034929', 'Reduced hepatic cystathionine gamma-lyase activity', 'XPO:0101547', 'abnormal lampbrush chromosome', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(629068, 'HP:0034929', 'Reduced hepatic cystathionine gamma-lyase activity', 'XPO:0141775', 'abnormal nitrogen compound metabolic process', 0.5238095238095238, 4.758907843651163, 1.5788480773767701, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(629069, 'HP:0034929', 'Reduced hepatic cystathionine gamma-lyase activity', 'XPO:0141884', 'abnormal phosphagen metabolic process', 0.4230769230769231, 4.758907843651163, 1.418937661667548, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(629070, 'HP:0034929', 'Reduced hepatic cystathionine gamma-lyase activity', 'XPO:0131666', 'abnormal adherens junction', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(629071, 'HP:0034929', 'Reduced hepatic cystathionine gamma-lyase activity', 'XPO:0141866', 'abnormal dicarboxylic acid metabolic process', 0.4074074074074074, 4.758907843651163, 1.392413123563799, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(629072, 'HP:0034929', 'Reduced hepatic cystathionine gamma-lyase activity', 'XPO:0100084', 'abnormal anatomical group', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(629073, 'HP:0034929', 'Reduced hepatic cystathionine gamma-lyase activity', 'XPO:0141266', 'abnormal surface breathing', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(629074, 'HP:0034929', 'Reduced hepatic cystathionine gamma-lyase activity', 'XPO:0141883', 'abnormal glycerol metabolic process', 0.4230769230769231, 4.758907843651163, 1.418937661667548, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(629075, 'HP:0034929', 'Reduced hepatic cystathionine gamma-lyase activity', 'XPO:0100317', 'abnormal respiratory system', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(629076, 'HP:0034929', 'Reduced hepatic cystathionine gamma-lyase activity', 'XPO:0100344', 'abnormal portion of organism substance', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(629077, 'HP:0034929', 'Reduced hepatic cystathionine gamma-lyase activity', 'XPO:0141788', 'abnormal hormone biosynthetic process', 0.44, 4.758907843651163, 1.447038165082909, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(629078, 'HP:0034929', 'Reduced hepatic cystathionine gamma-lyase activity', 'XPO:0141872', 'abnormal cholesterol metabolic process', 0.4074074074074074, 4.758907843651163, 1.392413123563799, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(629079, 'HP:0034929', 'Reduced hepatic cystathionine gamma-lyase activity', 'XPO:0141782', 'abnormal methylation', 0.5238095238095238, 4.758907843651163, 1.5788480773767701, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(629080, 'HP:0034929', 'Reduced hepatic cystathionine gamma-lyase activity', 'XPO:0107312', 'abnormal filopodium', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(629081, 'HP:0034929', 'Reduced hepatic cystathionine gamma-lyase activity', 'XPO:0131691', 'abnormal molecular function', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(629082, 'HP:0034929', 'Reduced hepatic cystathionine gamma-lyase activity', 'XPO:0115512', 'abnormally semi-erect whole organism', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(629083, 'HP:0034929', 'Reduced hepatic cystathionine gamma-lyase activity', 'XPO:0101409', 'abnormal perivitelline space', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(629084, 'HP:0034929', 'Reduced hepatic cystathionine gamma-lyase activity', 'XPO:0131745', 'abnormal axis elongation', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(629085, 'HP:0034929', 'Reduced hepatic cystathionine gamma-lyase activity', 'XPO:0100715', 'abnormal ciliated cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(629086, 'HP:0034929', 'Reduced hepatic cystathionine gamma-lyase activity', 'XPO:0100225', 'abnormal endocrine system', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(629087, 'HP:0034929', 'Reduced hepatic cystathionine gamma-lyase activity', 'XPO:0100232', 'abnormal lymphatic system', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(629088, 'HP:0034929', 'Reduced hepatic cystathionine gamma-lyase activity', 'XPO:0100549', 'abnormal mitotic cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(629089, 'HP:0034929', 'Reduced hepatic cystathionine gamma-lyase activity', 'XPO:0141778', 'abnormal biosynthetic process', 0.5238095238095238, 4.758907843651163, 1.5788480773767701, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(629090, 'HP:0034929', 'Reduced hepatic cystathionine gamma-lyase activity', 'XPO:0141777', 'abnormal catabolic process', 0.5238095238095238, 4.758907843651163, 1.5788480773767701, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(629091, 'HP:0034929', 'Reduced hepatic cystathionine gamma-lyase activity', 'XPO:0141600', 'absent metamorphosis', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(629092, 'HP:0034929', 'Reduced hepatic cystathionine gamma-lyase activity', 'XPO:0101220', 'abnormal centriole', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(629093, 'HP:0034929', 'Reduced hepatic cystathionine gamma-lyase activity', 'XPO:0100285', 'abnormal progenitor cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(629094, 'HP:0034929', 'Reduced hepatic cystathionine gamma-lyase activity', 'XPO:0141272', 'absent surface breathing', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(629095, 'HP:0034929', 'Reduced hepatic cystathionine gamma-lyase activity', 'XPO:0141854', 'abnormal glutathione metabolic process', 0.4230769230769231, 4.758907843651163, 1.418937661667548, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(629096, 'HP:0034929', 'Reduced hepatic cystathionine gamma-lyase activity', 'XPO:0141904', 'abnormal glucosamine metabolic process', 0.5238095238095238, 4.758907843651163, 1.5788480773767701, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(629097, 'HP:0034929', 'Reduced hepatic cystathionine gamma-lyase activity', 'XPO:0131725', 'abnormal phosphorylation of RNA polymerase II C-terminal domain', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(629098, 'HP:0034929', 'Reduced hepatic cystathionine gamma-lyase activity', 'XPO:0141263', 'abnormal visually guided collision avoidance behavior', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(629099, 'HP:0034929', 'Reduced hepatic cystathionine gamma-lyase activity', 'XPO:0100626', 'abnormal primordial germ cell', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(629100, 'HP:0034929', 'Reduced hepatic cystathionine gamma-lyase activity', 'XPO:0100791', 'abnormal multiciliated cell precursor', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(629101, 'HP:0034929', 'Reduced hepatic cystathionine gamma-lyase activity', 'XPO:0100585', 'abnormal elastica externa', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(629102, 'HP:0034929', 'Reduced hepatic cystathionine gamma-lyase activity', 'XPO:0141265', 'abnormal escape behavior', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(629103, 'HP:0034929', 'Reduced hepatic cystathionine gamma-lyase activity', 'XPO:0141264', 'abnormal schooling behavior', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(629104, 'HP:0034929', 'Reduced hepatic cystathionine gamma-lyase activity', 'XPO:0100599', 'abnormal adult immune system', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(629105, 'HP:0034929', 'Reduced hepatic cystathionine gamma-lyase activity', 'XPO:0100172', 'abnormal stem cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(629106, 'HP:0034929', 'Reduced hepatic cystathionine gamma-lyase activity', 'XPO:0107260', 'abnormal anterior-posterior axis', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(629107, 'HP:0034929', 'Reduced hepatic cystathionine gamma-lyase activity', 'XPO:0100653', 'abnormal myoblast', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(629108, 'HP:0034929', 'Reduced hepatic cystathionine gamma-lyase activity', 'XPO:0100372', 'abnormal hematological system', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(629109, 'HP:0034929', 'Reduced hepatic cystathionine gamma-lyase activity', 'XPO:0100377', 'abnormal connective tissue', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(629110, 'HP:0034929', 'Reduced hepatic cystathionine gamma-lyase activity', 'XPO:0100386', 'abnormal limb', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(629111, 'HP:0034929', 'Reduced hepatic cystathionine gamma-lyase activity', 'XPO:0101071', 'abnormal endoplasmic reticulum', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(629112, 'HP:0034929', 'Reduced hepatic cystathionine gamma-lyase activity', 'XPO:0100907', 'abnormal cytoplasm', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(629113, 'HP:0034929', 'Reduced hepatic cystathionine gamma-lyase activity', 'XPO:0131723', 'abnormal pathway-restricted SMAD protein phosphorylation', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(629114, 'HP:0034929', 'Reduced hepatic cystathionine gamma-lyase activity', 'XPO:0141786', 'abnormal pigment metabolic process', 0.5238095238095238, 4.758907843651163, 1.5788480773767701, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(629115, 'HP:0034929', 'Reduced hepatic cystathionine gamma-lyase activity', 'XPO:0115505', 'dead whole organism', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(629116, 'HP:0034929', 'Reduced hepatic cystathionine gamma-lyase activity', 'XPO:0131729', 'abnormal regulation of growth rate', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(629117, 'HP:0034929', 'Reduced hepatic cystathionine gamma-lyase activity', 'XPO:0100176', 'abnormal stage VI oocyte', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(629118, 'HP:0034929', 'Reduced hepatic cystathionine gamma-lyase activity', 'XPO:0141783', 'abnormal collagen metabolic process', 0.5238095238095238, 4.758907843651163, 1.5788480773767701, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(629119, 'HP:0034929', 'Reduced hepatic cystathionine gamma-lyase activity', 'XPO:0141790', 'abnormal cellular metabolic process', 0.5, 4.758907843651163, 1.5425478669479211, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(629120, 'HP:0034929', 'Reduced hepatic cystathionine gamma-lyase activity', 'XPO:0101061', 'abnormal plasma membrane', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(629121, 'HP:0034929', 'Reduced hepatic cystathionine gamma-lyase activity', 'XPO:0107261', 'abnormal dorsal-ventral axis', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(629122, 'HP:0034929', 'Reduced hepatic cystathionine gamma-lyase activity', 'XPO:0100917', 'abnormal stage III oocyte', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(629123, 'HP:0034929', 'Reduced hepatic cystathionine gamma-lyase activity', 'XPO:0101448', 'abnormal myelin accumulating cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(629124, 'HP:0034929', 'Reduced hepatic cystathionine gamma-lyase activity', 'XPO:0141789', 'abnormal hormone catabolic process', 0.44, 4.758907843651163, 1.447038165082909, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(629125, 'HP:0034929', 'Reduced hepatic cystathionine gamma-lyase activity', 'XPO:0141892', 'abnormal inositol metabolic process', 0.4782608695652174, 4.758907843651163, 1.508641575552437, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(629126, 'HP:0034929', 'Reduced hepatic cystathionine gamma-lyase activity', 'XPO:0100976', 'abnormal multiciliated cell', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(629127, 'HP:0034929', 'Reduced hepatic cystathionine gamma-lyase activity', 'XPO:0100728', 'abnormal cell condensation', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(629128, 'HP:0034929', 'Reduced hepatic cystathionine gamma-lyase activity', 'XPO:0141745', 'abnormal creatinine homeostasis', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(629129, 'HP:0034929', 'Reduced hepatic cystathionine gamma-lyase activity', 'XPO:0101110', 'abnormal cell-free extract', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(629130, 'HP:0034929', 'Reduced hepatic cystathionine gamma-lyase activity', 'XPO:0100392', 'abnormal cilium', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(629131, 'HP:0034929', 'Reduced hepatic cystathionine gamma-lyase activity', 'XPO:0141315', 'abnormal anatomical region', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(629132, 'HP:0034929', 'Reduced hepatic cystathionine gamma-lyase activity', 'XPO:0100274', 'abnormal sensory system', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(629133, 'HP:0034929', 'Reduced hepatic cystathionine gamma-lyase activity', 'XPO:0101109', 'abnormal egg cell-free extract', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(629134, 'HP:0034929', 'Reduced hepatic cystathionine gamma-lyase activity', 'XPO:0141794', 'abnormal prosthetic group metabolic process', 0.5238095238095238, 4.758907843651163, 1.5788480773767701, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(629135, 'HP:0034929', 'Reduced hepatic cystathionine gamma-lyase activity', 'XPO:0101468', 'abnormal stage I oocyte', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(629136, 'HP:0011251', 'Underdeveloped antitragus', 'XPO:0126939', 'abnormally localised auditory apparatus', 0.4782608695652174, 10.484129389061598, 2.2392295188852014, 'UPHENO:0005986', 'abnormal shape of external ear'),
(629137, 'HP:0011251', 'Underdeveloped antitragus', 'XPO:0131600', 'decreased size of the intercanthal region', 0.42105263157894735, 5.653868323764771, 1.5429115776096853, 'UPHENO:0012541', 'decreased size of the anatomical entity in the independent continuant'),
(629138, 'HP:0011251', 'Underdeveloped antitragus', 'XPO:0129311', 'decreased size of the lateral nasal prominence', 0.4067796610169492, 5.653868323764771, 1.5165350771332327, 'UPHENO:0012541', 'decreased size of the anatomical entity in the independent continuant'),
(629139, 'HP:0011251', 'Underdeveloped antitragus', 'XPO:0103342', 'decreased size of the head', 0.4067796610169492, 5.653868323764771, 1.5165350771332327, 'UPHENO:0012541', 'decreased size of the anatomical entity in the independent continuant'),
(629140, 'HP:0011251', 'Underdeveloped antitragus', 'XPO:0129164', 'decreased size of the medial nasal prominence', 0.4067796610169492, 5.653868323764771, 1.5165350771332327, 'UPHENO:0012541', 'decreased size of the anatomical entity in the independent continuant'),
(629141, 'HP:0011251', 'Underdeveloped antitragus', 'XPO:0102259', 'abnormal pharyngeal region morphology', 0.40384615384615385, 4.5318002188002176, 1.3528303989641963, 'UPHENO:0087907', 'abnormal head morphology'),
(629142, 'HP:0011251', 'Underdeveloped antitragus', 'XPO:0103358', 'decreased size of the pharyngeal region', 0.4444444444444444, 5.653868323764771, 1.5851909557266834, 'UPHENO:0012541', 'decreased size of the anatomical entity in the independent continuant'),
(629143, 'HP:0011251', 'Underdeveloped antitragus', 'XPO:0128582', 'decreased size of the head region', 0.42105263157894735, 5.653868323764771, 1.5429115776096853, 'UPHENO:0012541', 'decreased size of the anatomical entity in the independent continuant'),
(629144, 'HP:0034106', 'Anti-Su antigen/argonaute 2 antibody positivity', 'XPO:0100232', 'abnormal lymphatic system', 0.48148148148148145, 5.64885357140806, 1.6491871895674883, 'HP:0002715', 'Abnormality of the immune system'),
(629145, 'HP:0034106', 'Anti-Su antigen/argonaute 2 antibody positivity', 'XPO:0101518', 'abnormal B cell', 0.40625, 5.64885357140806, 1.5148751642906173, 'HP:0002715', 'Abnormality of the immune system'),
(629146, 'HP:0034106', 'Anti-Su antigen/argonaute 2 antibody positivity', 'XPO:0100581', 'abnormal immune system', 0.48148148148148145, 5.64885357140806, 1.6491871895674883, 'HP:0002715', 'Abnormality of the immune system'),
(629147, 'HP:0034106', 'Anti-Su antigen/argonaute 2 antibody positivity', 'XPO:0100004', 'abnormal cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(629148, 'HP:0034106', 'Anti-Su antigen/argonaute 2 antibody positivity', 'XPO:0101083', 'abnormal T cell', 0.40625, 5.64885357140806, 1.5148751642906173, 'HP:0002715', 'Abnormality of the immune system'),
(629149, 'HP:0034106', 'Anti-Su antigen/argonaute 2 antibody positivity', 'XPO:0100599', 'abnormal adult immune system', 0.4642857142857143, 5.64885357140806, 1.6194696710023933, 'HP:0002715', 'Abnormality of the immune system'),
(629150, 'HP:0034106', 'Anti-Su antigen/argonaute 2 antibody positivity', 'XPO:0100540', 'abnormal left lymph heart', 0.40625, 5.64885357140806, 1.5148751642906173, 'HP:0002715', 'Abnormality of the immune system'),
(629151, 'HP:0034106', 'Anti-Su antigen/argonaute 2 antibody positivity', 'XPO:0101029', 'abnormal right spleen primordium', 0.41935483870967744, 5.64885357140806, 1.5391147060347428, 'HP:0002715', 'Abnormality of the immune system'),
(629152, 'HP:0034106', 'Anti-Su antigen/argonaute 2 antibody positivity', 'XPO:0141497', 'abnormal lymphoblast', 0.41935483870967744, 5.64885357140806, 1.5391147060347428, 'HP:0002715', 'Abnormality of the immune system'),
(629153, 'HP:0034106', 'Anti-Su antigen/argonaute 2 antibody positivity', 'XPO:0101451', 'abnormal dorsal lymph space', 0.4482758620689655, 5.64885357140806, 1.5913028324062968, 'HP:0002715', 'Abnormality of the immune system'),
(629154, 'HP:0034106', 'Anti-Su antigen/argonaute 2 antibody positivity', 'XPO:0100745', 'abnormal anterior lymph sac', 0.43333333333333335, 5.64885357140806, 1.5645563421015427, 'HP:0002715', 'Abnormality of the immune system'),
(629155, 'HP:0034106', 'Anti-Su antigen/argonaute 2 antibody positivity', 'XPO:0100449', 'abnormal lymphocyte', 0.41935483870967744, 5.64885357140806, 1.5391147060347428, 'HP:0002715', 'Abnormality of the immune system'),
(629156, 'HP:0034106', 'Anti-Su antigen/argonaute 2 antibody positivity', 'XPO:0101221', 'abnormal larval immune system', 0.4642857142857143, 5.64885357140806, 1.6194696710023933, 'HP:0002715', 'Abnormality of the immune system'),
(629157, 'HP:0034106', 'Anti-Su antigen/argonaute 2 antibody positivity', 'XPO:0100242', 'abnormal right lymph heart', 0.40625, 5.64885357140806, 1.5148751642906173, 'HP:0002715', 'Abnormality of the immune system'),
(629158, 'HP:0006938', 'Impaired vibration sensation at ankles', 'XPO:0100642', 'abnormal gustatory system', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(629159, 'HP:0006938', 'Impaired vibration sensation at ankles', 'XPO:0100032', 'abnormal nervous system', 0.43333333333333335, 3.94131651835137, 1.3068679445984308, 'UPHENO:0004523', 'abnormal nervous system'),
(629160, 'HP:0006938', 'Impaired vibration sensation at ankles', 'XPO:0100427', 'abnormal olfactory system', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(629161, 'HP:0006938', 'Impaired vibration sensation at ankles', 'XPO:0107253', 'abnormal enteric nervous system', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(629162, 'HP:0006938', 'Impaired vibration sensation at ankles', 'XPO:0100274', 'abnormal sensory system', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(629163, 'HP:0006938', 'Impaired vibration sensation at ankles', 'XPO:0100273', 'abnormal visual system', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(629164, 'HP:0006938', 'Impaired vibration sensation at ankles', 'XPO:0100587', 'abnormal vestibuloauditory system', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(629165, 'HP:0006938', 'Impaired vibration sensation at ankles', 'XPO:0100031', 'abnormal central nervous system', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(629166, 'HP:0001593', 'Maxillary lateral incisor microdontia', 'XPO:0101659', 'abnormal lower jaw morphology', 0.5340909090909091, 8.608423498638606, 2.1442203086967155, 'UPHENO:0088116', 'abnormal jaw skeleton morphology'),
(629167, 'HP:0001593', 'Maxillary lateral incisor microdontia', 'XPO:0130466', 'increased size of the tooth', 0.42990654205607476, 9.872199840740173, 2.060127009681476, 'HP:0006482', 'Abnormal dental morphology'),
(629168, 'HP:0001593', 'Maxillary lateral incisor microdontia', 'XPO:0102337', 'abnormal processus retroarticularis of Meckels cartilage morphology', 0.415929203539823, 8.608423498638606, 1.8922195246646865, 'UPHENO:0088116', 'abnormal jaw skeleton morphology'),
(629169, 'HP:0001593', 'Maxillary lateral incisor microdontia', 'XPO:0102861', 'abnormal cementum morphology', 0.42857142857142855, 9.872199840740173, 2.0569255671726783, 'HP:0006482', 'Abnormal dental morphology'),
(629170, 'HP:0001593', 'Maxillary lateral incisor microdontia', 'XPO:0102890', 'abnormal dentine morphology', 0.4205607476635514, 9.872199840740173, 2.037611284348828, 'HP:0006482', 'Abnormal dental morphology'),
(629171, 'HP:0001593', 'Maxillary lateral incisor microdontia', 'XPO:0128880', 'decreased size of the lower jaw', 0.5434782608695652, 8.608423498638606, 2.1629819767785414, 'UPHENO:0088116', 'abnormal jaw skeleton morphology'),
(629172, 'HP:0001593', 'Maxillary lateral incisor microdontia', 'XPO:0140897', 'abnormally necrotic lower jaw', 0.5053763440860215, 8.608423498638606, 2.085783688709397, 'UPHENO:0088116', 'abnormal jaw skeleton morphology'),
(629173, 'HP:0001593', 'Maxillary lateral incisor microdontia', 'XPO:0103199', 'abnormal tongue morphology', 0.40229885057471265, 7.884497199543557, 1.7809896576723612, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(629174, 'HP:0001593', 'Maxillary lateral incisor microdontia', 'XPO:0101816', 'abnormal tooth morphology', 0.46875, 9.872199840740173, 2.1511842495116396, 'HP:0006482', 'Abnormal dental morphology'),
(629175, 'HP:0001593', 'Maxillary lateral incisor microdontia', 'XPO:0139736', 'abnormally necrotic tooth', 0.4326923076923077, 9.872199840740173, 2.0667909742132844, 'HP:0006482', 'Abnormal dental morphology'),
(629176, 'HP:0001593', 'Maxillary lateral incisor microdontia', 'XPO:0103352', 'decreased size of the mouth', 0.40860215053763443, 7.884497199543557, 1.794887882749631, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(629177, 'HP:0001593', 'Maxillary lateral incisor microdontia', 'XPO:0103350', 'decreased size of the Meckels cartilage', 0.4166666666666667, 8.608423498638606, 1.8938962813292477, 'UPHENO:0088116', 'abnormal jaw skeleton morphology'),
(629178, 'HP:0001593', 'Maxillary lateral incisor microdontia', 'XPO:0102398', 'abnormal Meckels cartilage morphology', 0.42342342342342343, 8.608423498638606, 1.9091904431125257, 'UPHENO:0088116', 'abnormal jaw skeleton morphology'),
(629179, 'HP:0001593', 'Maxillary lateral incisor microdontia', 'XPO:0115393', 'abnormally decreased volume of oral cavity', 0.4175824175824176, 7.884497199543557, 1.8145047263667295, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(629180, 'HP:0001593', 'Maxillary lateral incisor microdontia', 'XPO:0130701', 'increased size of the upper jaw', 0.5319148936170213, 8.81758714901448, 2.165688327143786, 'UPHENO:0087585', 'abnormal midface morphology'),
(629181, 'HP:0001593', 'Maxillary lateral incisor microdontia', 'XPO:0129990', 'increased size of the cementum', 0.40350877192982454, 9.872199840740173, 1.9958755557355965, 'HP:0006482', 'Abnormal dental morphology'),
(629182, 'HP:0001593', 'Maxillary lateral incisor microdontia', 'XPO:0140639', 'abnormally necrotic upper jaw', 0.5268817204301075, 8.81758714901448, 2.1554177059482362, 'UPHENO:0087585', 'abnormal midface morphology'),
(629183, 'HP:0001593', 'Maxillary lateral incisor microdontia', 'XPO:0103138', 'abnormal upper jaw morphology', 0.5568181818181818, 8.81758714901448, 2.215805236102128, 'UPHENO:0087585', 'abnormal midface morphology'),
(629184, 'HP:0001593', 'Maxillary lateral incisor microdontia', 'XPO:0128989', 'decreased size of the tooth', 0.4854368932038835, 13.511610125483706, 2.56106111631428, 'UPHENO:0068923', 'decreased size of the calcareous tooth'),
(629185, 'HP:0001593', 'Maxillary lateral incisor microdontia', 'XPO:0129449', 'decreased size of the dentine', 0.41739130434782606, 9.872199840740173, 2.0299188083046427, 'HP:0006482', 'Abnormal dental morphology'),
(629186, 'HP:0001593', 'Maxillary lateral incisor microdontia', 'XPO:0128953', 'decreased size of the processus retroarticularis of Meckels cartilage', 0.4132231404958678, 8.608423498638606, 1.8860540270166892, 'UPHENO:0088116', 'abnormal jaw skeleton morphology'),
(629187, 'HP:0001593', 'Maxillary lateral incisor microdontia', 'XPO:0130358', 'increased size of the lower jaw', 0.5106382978723404, 8.608423498638606, 2.096614109155301, 'UPHENO:0088116', 'abnormal jaw skeleton morphology'),
(629188, 'HP:0001593', 'Maxillary lateral incisor microdontia', 'XPO:0129225', 'decreased size of the upper jaw', 0.5652173913043478, 8.81758714901448, 2.232454614536364, 'UPHENO:0087585', 'abnormal midface morphology'),
(629189, 'HP:0001593', 'Maxillary lateral incisor microdontia', 'XPO:0129152', 'decreased size of the oral cavity', 0.42696629213483145, 7.884497199543557, 1.834779151461171, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(629190, 'HP:0001593', 'Maxillary lateral incisor microdontia', 'XPO:0103096', 'abnormal oral cavity morphology', 0.40229885057471265, 7.884497199543557, 1.7809896576723612, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(629191, 'HP:0001593', 'Maxillary lateral incisor microdontia', 'XPO:0128510', 'decreased size of the cementum', 0.42857142857142855, 9.872199840740173, 2.0569255671726783, 'HP:0006482', 'Abnormal dental morphology'),
(629192, 'HP:0000175', 'Cleft palate', 'XPO:0141830', 'increased width of mouth', 0.45454545454545453, 7.884497199543557, 1.8931091789510952, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(629193, 'HP:0000175', 'Cleft palate', 'XPO:0102279', 'abnormal mouth morphology', 0.5238095238095238, 7.312692920701687, 1.9571556393291838, 'UPHENO:0076800', 'abnormal mouth morphology'),
(629194, 'HP:0000175', 'Cleft palate', 'XPO:0130132', 'increased size of the oral epithelium', 0.4074074074074074, 7.312692920701687, 1.7260490329042149, 'UPHENO:0076800', 'abnormal mouth morphology'),
(629195, 'HP:0000175', 'Cleft palate', 'XPO:0141311', 'abnormal roof of mouth morphology', 0.5, 7.312692920701687, 1.9121575406725366, 'UPHENO:0076800', 'abnormal mouth morphology'),
(629196, 'HP:0000175', 'Cleft palate', 'XPO:0129225', 'decreased size of the upper jaw', 0.42857142857142855, 8.81758714901448, 1.9439562549106413, 'UPHENO:0087585', 'abnormal midface morphology'),
(629197, 'HP:0000175', 'Cleft palate', 'XPO:0140789', 'abnormally necrotic roof of mouth', 0.4647887323943662, 7.312692920701687, 1.8435990000545652, 'UPHENO:0076800', 'abnormal mouth morphology'),
(629198, 'HP:0000175', 'Cleft palate', 'XPO:0103828', 'decreased width of the mouth', 0.45454545454545453, 7.884497199543557, 1.8931091789510952, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(629199, 'HP:0000175', 'Cleft palate', 'XPO:0102525', 'abnormal hyoid arch morphology', 0.4090909090909091, 5.725717590856133, 1.5304701939081158, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(629200, 'HP:0000175', 'Cleft palate', 'XPO:0126089', 'absent tongue', 0.4782608695652174, 7.884497199543557, 1.9418667530853457, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(629201, 'HP:0000175', 'Cleft palate', 'XPO:0102223', 'abnormal pharyngeal arch morphology', 0.42857142857142855, 5.725717590856133, 1.5664861849086864, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(629202, 'HP:0000175', 'Cleft palate', 'XPO:0140626', 'abnormally necrotic tongue', 0.5147058823529411, 7.884497199543557, 2.0144967331818533, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(629203, 'HP:0000175', 'Cleft palate', 'XPO:0127750', 'abnormally localised tongue', 0.4925373134328358, 7.884497199543557, 1.970636716503552, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(629204, 'HP:0000175', 'Cleft palate', 'XPO:0102735', 'abnormal pharyngeal mesenchyme morphology', 0.40298507462686567, 5.725717590856133, 1.5190058362769763, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(629205, 'HP:0000175', 'Cleft palate', 'XPO:0140897', 'abnormally necrotic lower jaw', 0.4146341463414634, 7.312692920701687, 1.7412903797564627, 'UPHENO:0076800', 'abnormal mouth morphology'),
(629206, 'HP:0000175', 'Cleft palate', 'XPO:0130358', 'increased size of the lower jaw', 0.40476190476190477, 7.312692920701687, 1.7204358504524693, 'UPHENO:0076800', 'abnormal mouth morphology'),
(629207, 'HP:0000175', 'Cleft palate', 'XPO:0115393', 'abnormally decreased volume of oral cavity', 0.5, 7.884497199543557, 1.9855096574360394, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(629208, 'HP:0000175', 'Cleft palate', 'XPO:0128653', 'decreased size of the oral epithelium', 0.4074074074074074, 7.312692920701687, 1.7260490329042149, 'UPHENO:0076800', 'abnormal mouth morphology'),
(629209, 'HP:0000175', 'Cleft palate', 'XPO:0102960', 'abnormal oral epithelium morphology', 0.4583333333333333, 7.312692920701687, 1.830751463740579, 'UPHENO:0076800', 'abnormal mouth morphology'),
(629210, 'HP:0000175', 'Cleft palate', 'XPO:0128105', 'decreased size of the tongue', 0.4605263157894737, 7.884497199543557, 1.9055231426456665, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(629211, 'HP:0000175', 'Cleft palate', 'XPO:0103199', 'abnormal tongue morphology', 0.5555555555555556, 7.884497199543557, 2.0929109445861864, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(629212, 'HP:0000175', 'Cleft palate', 'XPO:0103096', 'abnormal oral cavity morphology', 0.5555555555555556, 7.884497199543557, 2.0929109445861864, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(629213, 'HP:0000175', 'Cleft palate', 'XPO:0103138', 'abnormal upper jaw morphology', 0.4675324675324675, 8.81758714901448, 2.0303960888115684, 'UPHENO:0087585', 'abnormal midface morphology'),
(629214, 'HP:0000175', 'Cleft palate', 'XPO:0115558', 'abnormally incomplete structure of mouth', 0.515625, 7.312692920701687, 1.9418051620172418, 'UPHENO:0076800', 'abnormal mouth morphology'),
(629215, 'HP:0000175', 'Cleft palate', 'XPO:0102204', 'abnormal branchial arch morphology', 0.4153846153846154, 5.725717590856133, 1.5421981063659433, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(629216, 'HP:0000175', 'Cleft palate', 'XPO:0101659', 'abnormal lower jaw morphology', 0.44155844155844154, 7.312692920701687, 1.7969366404134801, 'UPHENO:0076800', 'abnormal mouth morphology'),
(629217, 'HP:0000175', 'Cleft palate', 'XPO:0129152', 'decreased size of the oral cavity', 0.5147058823529411, 7.884497199543557, 2.0144967331818533, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(629218, 'HP:0000175', 'Cleft palate', 'XPO:0103352', 'decreased size of the mouth', 0.4861111111111111, 7.884497199543557, 1.9577389239177327, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(629219, 'HP:0000175', 'Cleft palate', 'XPO:0101816', 'abnormal tooth morphology', 0.4268292682926829, 7.884497199543557, 1.8344847152639032, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(629220, 'HP:0000175', 'Cleft palate', 'XPO:0140639', 'abnormally necrotic upper jaw', 0.43902439024390244, 8.81758714901448, 1.9675202213747518, 'UPHENO:0087585', 'abnormal midface morphology'),
(629221, 'HP:0000175', 'Cleft palate', 'XPO:0131611', 'increased size of the roof of mouth', 0.4520547945205479, 7.312692920701687, 1.8181688303509294, 'UPHENO:0076800', 'abnormal mouth morphology'),
(629222, 'HP:0000175', 'Cleft palate', 'XPO:0130628', 'increased size of the oral cavity', 0.5147058823529411, 7.884497199543557, 2.0144967331818533, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(629223, 'HP:0000175', 'Cleft palate', 'XPO:0102445', 'abnormal branchial arch 3 morphology', 0.40298507462686567, 5.725717590856133, 1.5190058362769763, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(629224, 'HP:0000175', 'Cleft palate', 'XPO:0128880', 'decreased size of the lower jaw', 0.40476190476190477, 7.312692920701687, 1.7204358504524693, 'UPHENO:0076800', 'abnormal mouth morphology'),
(629225, 'HP:0000175', 'Cleft palate', 'XPO:0131573', 'decreased size of the roof of mouth', 0.4520547945205479, 7.312692920701687, 1.8181688303509294, 'UPHENO:0076800', 'abnormal mouth morphology'),
(629226, 'HP:0000175', 'Cleft palate', 'XPO:0129585', 'increased size of the tongue', 0.43209876543209874, 7.884497199543557, 1.8457739585267778, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(629227, 'HP:0000175', 'Cleft palate', 'XPO:0103735', 'increased size of the mouth', 0.4861111111111111, 7.884497199543557, 1.9577389239177327, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(629228, 'HP:0000175', 'Cleft palate', 'XPO:0101567', 'abnormal tongue', 0.5614035087719298, 7.884497199543557, 2.103897429231332, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(629229, 'HP:0000175', 'Cleft palate', 'XPO:0141009', 'abnormally necrotic oral epithelium', 0.4177215189873418, 7.312692920701687, 1.7477611949930372, 'UPHENO:0076800', 'abnormal mouth morphology'),
(629230, 'HP:0000175', 'Cleft palate', 'XPO:0130701', 'increased size of the upper jaw', 0.42857142857142855, 8.81758714901448, 1.9439562549106413, 'UPHENO:0087585', 'abnormal midface morphology'),
(629231, 'HP:0003260', 'Hydroxyprolinemia', 'XPO:0141848', 'abnormal proline metabolic process', 0.4215686274509804, 14.30515924801628, 2.455729290792029, 'UPHENO:0078636', 'abnormal proline metabolic process'),
(629232, 'HP:0003260', 'Hydroxyprolinemia', 'XPO:0141869', 'abnormal alpha-amino acid metabolic process', 0.40594059405940597, 10.156767408123608, 2.030528058258962, 'UPHENO:0050249', 'abnormal alpha-amino acid metabolic process'),
(629233, 'HP:0003260', 'Hydroxyprolinemia', 'XPO:0141847', 'abnormal arginine metabolic process', 0.4077669902912621, 12.568193653850074, 2.263822983280315, 'UPHENO:0078648', 'abnormal glutamine family amino acid metabolic process'),
(629234, 'HP:0003260', 'Hydroxyprolinemia', 'XPO:0141882', 'abnormal gamma-aminobutyric acid metabolic process', 0.4019607843137255, 10.553838360873003, 2.059667241341862, 'UPHENO:0050484', 'abnormal monocarboxylic acid metabolic process'),
(629235, 'HP:0004385', 'Protracted diarrhea', 'XPO:0126608', 'abnormally localised foregut', 0.41025641025641024, 5.05060299610679, 1.4394590146346793, 'HP:0025031', 'Abnormality of the digestive system'),
(629236, 'HP:0004385', 'Protracted diarrhea', 'XPO:0101601', 'abnormal proctodeum', 0.4411764705882353, 5.05060299610679, 1.4927180591674907, 'HP:0025031', 'Abnormality of the digestive system'),
(629237, 'HP:0004385', 'Protracted diarrhea', 'XPO:0107308', 'abnormal anterior hindgut endoderm', 0.4166666666666667, 5.05060299610679, 1.45066119926208, 'HP:0025031', 'Abnormality of the digestive system'),
(629238, 'HP:0004385', 'Protracted diarrhea', 'XPO:0126837', 'abnormally localised midgut', 0.41025641025641024, 5.05060299610679, 1.4394590146346793, 'HP:0025031', 'Abnormality of the digestive system'),
(629239, 'HP:0004385', 'Protracted diarrhea', 'XPO:0115391', 'abnormally undifferentiated alimentary system', 0.5, 5.05060299610679, 1.5891197242666757, 'HP:0025031', 'Abnormality of the digestive system'),
(629240, 'HP:0004385', 'Protracted diarrhea', 'XPO:0127307', 'abnormally localised oral evagination', 0.41025641025641024, 5.05060299610679, 1.4394590146346793, 'HP:0025031', 'Abnormality of the digestive system'),
(629241, 'HP:0004385', 'Protracted diarrhea', 'XPO:0101381', 'abnormal ventral foregut', 0.45454545454545453, 5.05060299610679, 1.5151662069205463, 'HP:0025031', 'Abnormality of the digestive system'),
(629242, 'HP:0004385', 'Protracted diarrhea', 'XPO:0100718', 'abnormal ventral pancreatic bud', 0.4411764705882353, 5.05060299610679, 1.4927180591674907, 'HP:0025031', 'Abnormality of the digestive system'),
(629243, 'HP:0004385', 'Protracted diarrhea', 'XPO:0131683', 'abnormal stomach epithelium', 0.40540540540540543, 5.05060299610679, 1.4309233924911664, 'HP:0025031', 'Abnormality of the digestive system'),
(629244, 'HP:0004385', 'Protracted diarrhea', 'XPO:0100152', 'abnormal alimentary system', 0.5172413793103449, 5.05060299610679, 1.6162861318637973, 'HP:0025031', 'Abnormality of the digestive system'),
(629245, 'HP:0004385', 'Protracted diarrhea', 'XPO:0126499', 'abnormally localised liver and biliary system', 0.42105263157894735, 5.05060299610679, 1.4582762710032966, 'HP:0025031', 'Abnormality of the digestive system'),
(629246, 'HP:0004385', 'Protracted diarrhea', 'XPO:0101169', 'abnormal hepato-pancreatic duct', 0.4411764705882353, 5.05060299610679, 1.4927180591674907, 'HP:0025031', 'Abnormality of the digestive system'),
(629247, 'HP:0004385', 'Protracted diarrhea', 'XPO:0126520', 'abnormally localised hindgut', 0.41025641025641024, 5.05060299610679, 1.4394590146346793, 'HP:0025031', 'Abnormality of the digestive system'),
(629248, 'HP:0004385', 'Protracted diarrhea', 'XPO:0101377', 'abnormal manicotto glandulare', 0.46875, 5.05060299610679, 1.5386585568036393, 'HP:0025031', 'Abnormality of the digestive system'),
(629249, 'HP:0004385', 'Protracted diarrhea', 'XPO:0100215', 'abnormal first pancreatic bud', 0.42857142857142855, 5.05060299610679, 1.471238981671103, 'HP:0025031', 'Abnormality of the digestive system'),
(629250, 'HP:0004385', 'Protracted diarrhea', 'XPO:0142054', 'abnormal digestive tract', 0.4838709677419355, 5.05060299610679, 1.5632786569919361, 'HP:0025031', 'Abnormality of the digestive system'),
(629251, 'HP:0004385', 'Protracted diarrhea', 'XPO:0100986', 'abnormal gut epithelium', 0.45454545454545453, 5.05060299610679, 1.5151662069205463, 'HP:0025031', 'Abnormality of the digestive system'),
(629252, 'HP:0004385', 'Protracted diarrhea', 'XPO:0125745', 'absent pharyngeal cavity', 0.42105263157894735, 5.05060299610679, 1.4582762710032966, 'HP:0025031', 'Abnormality of the digestive system'),
(629253, 'HP:0004385', 'Protracted diarrhea', 'XPO:0100462', 'abnormal anterior foregut', 0.45454545454545453, 5.05060299610679, 1.5151662069205463, 'HP:0025031', 'Abnormality of the digestive system'),
(629254, 'HP:0004385', 'Protracted diarrhea', 'XPO:0102522', 'abnormal pharyngeal cavity morphology', 0.42105263157894735, 5.05060299610679, 1.4582762710032966, 'HP:0025031', 'Abnormality of the digestive system'),
(629255, 'HP:0004385', 'Protracted diarrhea', 'XPO:0127393', 'abnormally localised pharyngeal cavity', 0.43243243243243246, 5.05060299610679, 1.4778513250178418, 'HP:0025031', 'Abnormality of the digestive system'),
(629256, 'HP:0004385', 'Protracted diarrhea', 'XPO:0100216', 'abnormal hepato-pancreatic progenitor cell', 0.40540540540540543, 5.05060299610679, 1.4309233924911664, 'HP:0025031', 'Abnormality of the digestive system'),
(629257, 'HP:0004385', 'Protracted diarrhea', 'XPO:0141717', 'abnormal tracheoesophageal fold', 0.4166666666666667, 5.05060299610679, 1.45066119926208, 'HP:0025031', 'Abnormality of the digestive system'),
(629258, 'HP:0004385', 'Protracted diarrhea', 'XPO:0142027', 'abnormally localised digestive tract', 0.41025641025641024, 5.05060299610679, 1.4394590146346793, 'HP:0025031', 'Abnormality of the digestive system'),
(629259, 'HP:0004385', 'Protracted diarrhea', 'XPO:0124857', 'absent alimentary system', 0.42105263157894735, 5.05060299610679, 1.4582762710032966, 'HP:0025031', 'Abnormality of the digestive system'),
(629260, 'HP:0004385', 'Protracted diarrhea', 'XPO:0124888', 'absent liver and biliary system', 0.41025641025641024, 5.05060299610679, 1.4394590146346793, 'HP:0025031', 'Abnormality of the digestive system'),
(629261, 'HP:0004385', 'Protracted diarrhea', 'XPO:0101198', 'abnormal digestive enzyme secreting cell', 0.42857142857142855, 5.05060299610679, 1.471238981671103, 'HP:0025031', 'Abnormality of the digestive system'),
(629262, 'HP:0004385', 'Protracted diarrhea', 'XPO:0100621', 'abnormal peritoneum', 0.42857142857142855, 5.05060299610679, 1.471238981671103, 'HP:0025031', 'Abnormality of the digestive system'),
(629263, 'HP:0004385', 'Protracted diarrhea', 'XPO:0101101', 'abnormal posterior foregut', 0.45454545454545453, 5.05060299610679, 1.5151662069205463, 'HP:0025031', 'Abnormality of the digestive system'),
(629264, 'HP:0004385', 'Protracted diarrhea', 'XPO:0107288', 'abnormal larval alimentary system', 0.5, 5.05060299610679, 1.5891197242666757, 'HP:0025031', 'Abnormality of the digestive system'),
(629265, 'HP:0004385', 'Protracted diarrhea', 'XPO:0115392', 'abnormally incomplete structure of alimentary system', 0.41025641025641024, 5.05060299610679, 1.4394590146346793, 'HP:0025031', 'Abnormality of the digestive system'),
(629266, 'HP:0004385', 'Protracted diarrhea', 'XPO:0100214', 'abnormal second pancreatic bud', 0.4166666666666667, 5.05060299610679, 1.45066119926208, 'HP:0025031', 'Abnormality of the digestive system'),
(629267, 'HP:0004385', 'Protracted diarrhea', 'XPO:0100523', 'abnormal midgut', 0.46875, 5.05060299610679, 1.5386585568036393, 'HP:0025031', 'Abnormality of the digestive system'),
(629268, 'HP:0004385', 'Protracted diarrhea', 'XPO:0107306', 'abnormal ventral posterior hindgut endoderm', 0.40540540540540543, 5.05060299610679, 1.4309233924911664, 'HP:0025031', 'Abnormality of the digestive system'),
(629269, 'HP:0004385', 'Protracted diarrhea', 'XPO:0100591', 'abnormal pharyngeal arch', 0.40540540540540543, 5.05060299610679, 1.4309233924911664, 'HP:0025031', 'Abnormality of the digestive system'),
(629270, 'HP:0004385', 'Protracted diarrhea', 'XPO:0100486', 'abnormal oral evagination', 0.46875, 5.05060299610679, 1.5386585568036393, 'HP:0025031', 'Abnormality of the digestive system'),
(629271, 'HP:0004385', 'Protracted diarrhea', 'XPO:0101784', 'abnormal alimentary system morphology', 0.42105263157894735, 5.05060299610679, 1.4582762710032966, 'HP:0025031', 'Abnormality of the digestive system'),
(629272, 'HP:0004385', 'Protracted diarrhea', 'XPO:0107305', 'abnormal dorsal posterior hindgut endoderm', 0.40540540540540543, 5.05060299610679, 1.4309233924911664, 'HP:0025031', 'Abnormality of the digestive system'),
(629273, 'HP:0004385', 'Protracted diarrhea', 'XPO:0107304', 'abnormal hindgut endoderm', 0.42857142857142855, 5.05060299610679, 1.471238981671103, 'HP:0025031', 'Abnormality of the digestive system'),
(629274, 'HP:0004385', 'Protracted diarrhea', 'XPO:0100890', 'abnormal pharyngeal cavity', 0.4838709677419355, 5.05060299610679, 1.5632786569919361, 'HP:0025031', 'Abnormality of the digestive system'),
(629275, 'HP:0004385', 'Protracted diarrhea', 'XPO:0100130', 'abnormal mouth primordium', 0.40540540540540543, 5.05060299610679, 1.4309233924911664, 'HP:0025031', 'Abnormality of the digestive system'),
(629276, 'HP:0004385', 'Protracted diarrhea', 'XPO:0100156', 'abnormal foregut', 0.46875, 5.05060299610679, 1.5386585568036393, 'HP:0025031', 'Abnormality of the digestive system'),
(629277, 'HP:0004385', 'Protracted diarrhea', 'XPO:0107307', 'abnormal posterior hindgut endoderm', 0.4166666666666667, 5.05060299610679, 1.45066119926208, 'HP:0025031', 'Abnormality of the digestive system'),
(629278, 'HP:0004385', 'Protracted diarrhea', 'XPO:0101021', 'abnormal dorsal foregut', 0.45454545454545453, 5.05060299610679, 1.5151662069205463, 'HP:0025031', 'Abnormality of the digestive system'),
(629279, 'HP:0004385', 'Protracted diarrhea', 'XPO:0115495', 'abnormally protruding proctodeum', 0.4444444444444444, 5.05060299610679, 1.4982364441950171, 'HP:0025031', 'Abnormality of the digestive system'),
(629280, 'HP:0004385', 'Protracted diarrhea', 'XPO:0100493', 'abnormal liver and biliary system', 0.5, 5.05060299610679, 1.5891197242666757, 'HP:0025031', 'Abnormality of the digestive system'),
(629281, 'HP:0004385', 'Protracted diarrhea', 'XPO:0126466', 'abnormally localised alimentary system', 0.43243243243243246, 5.05060299610679, 1.4778513250178418, 'HP:0025031', 'Abnormality of the digestive system'),
(629282, 'HP:0004385', 'Protracted diarrhea', 'XPO:0100492', 'abnormal gall bladder primordium', 0.42857142857142855, 5.05060299610679, 1.471238981671103, 'HP:0025031', 'Abnormality of the digestive system'),
(629283, 'HP:0004385', 'Protracted diarrhea', 'XPO:0126705', 'abnormally localised larval alimentary system', 0.41025641025641024, 5.05060299610679, 1.4394590146346793, 'HP:0025031', 'Abnormality of the digestive system'),
(629284, 'HP:0004385', 'Protracted diarrhea', 'XPO:0131662', 'abnormal foregut epithelium', 0.40540540540540543, 5.05060299610679, 1.4309233924911664, 'HP:0025031', 'Abnormality of the digestive system'),
(629285, 'HP:0004385', 'Protracted diarrhea', 'XPO:0100735', 'abnormal hindgut', 0.46875, 5.05060299610679, 1.5386585568036393, 'HP:0025031', 'Abnormality of the digestive system'),
(629286, 'HP:0030775', 'Modic type vertebral endplate changes', 'XPO:0100253', 'abnormal vertebra', 0.423728813559322, 8.05344015541032, 1.8472884566637167, 'UPHENO:0002813', 'abnormal vertebral column'),
(629287, 'HP:0030775', 'Modic type vertebral endplate changes', 'XPO:0130060', 'increased size of the postcranial axial skeleton', 0.42592592592592593, 6.272837960958401, 1.6345532468244968, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(629288, 'HP:0030775', 'Modic type vertebral endplate changes', 'XPO:0141703', 'abnormally necrotic posterior notochord', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(629289, 'HP:0030775', 'Modic type vertebral endplate changes', 'XPO:0141708', 'decreased size of the posterior notochord', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(629290, 'HP:0030775', 'Modic type vertebral endplate changes', 'XPO:0103078', 'abnormal transverse process morphology', 0.4307692307692308, 8.748525470353618, 1.941287095519169, 'HP:0003468', 'Abnormal vertebral morphology'),
(629291, 'HP:0030775', 'Modic type vertebral endplate changes', 'XPO:0102130', 'abnormal endoskeleton morphology', 0.4444444444444444, 4.638757693672553, 1.4358516936218344, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(629292, 'HP:0030775', 'Modic type vertebral endplate changes', 'XPO:0140806', 'abnormally necrotic rib', 0.4117647058823529, 8.748525470353618, 1.8979815639790685, 'HP:0003468', 'Abnormal vertebral morphology'),
(629293, 'HP:0030775', 'Modic type vertebral endplate changes', 'XPO:0141699', 'abnormally necrotic anterior notochord', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(629294, 'HP:0030775', 'Modic type vertebral endplate changes', 'XPO:0127548', 'abnormally localised vertebral element', 0.423728813559322, 8.05344015541032, 1.8472884566637167, 'UPHENO:0002813', 'abnormal vertebral column'),
(629295, 'HP:0030775', 'Modic type vertebral endplate changes', 'XPO:0102093', 'abnormal craniofacial skeleton morphology', 0.4375, 6.211345574613551, 1.6484731386629958, 'UPHENO:0087089', 'abnormal axial skeleton plus cranial skeleton morphology'),
(629296, 'HP:0030775', 'Modic type vertebral endplate changes', 'XPO:0139889', 'abnormally necrotic cranial skeleton', 0.40384615384615385, 6.211345574613551, 1.5838017617482976, 'UPHENO:0087089', 'abnormal axial skeleton plus cranial skeleton morphology'),
(629297, 'HP:0030775', 'Modic type vertebral endplate changes', 'XPO:0128306', 'decreased size of the articular system', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(629298, 'HP:0030775', 'Modic type vertebral endplate changes', 'XPO:0130908', 'increased size of the notochordal sheath', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(629299, 'HP:0030775', 'Modic type vertebral endplate changes', 'XPO:0101713', 'abnormal anatomical entity in vitro morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(629300, 'HP:0030775', 'Modic type vertebral endplate changes', 'XPO:0102702', 'abnormal rib morphology', 0.4375, 8.748525470353618, 1.9563946159401757, 'HP:0003468', 'Abnormal vertebral morphology'),
(629301, 'HP:0030775', 'Modic type vertebral endplate changes', 'XPO:0102514', 'abnormal perichondrial cell morphology', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(629302, 'HP:0030775', 'Modic type vertebral endplate changes', 'XPO:0100226', 'abnormal vertebral element', 0.5208333333333334, 8.05344015541032, 2.048047870764469, 'UPHENO:0002813', 'abnormal vertebral column'),
(629303, 'HP:0030775', 'Modic type vertebral endplate changes', 'XPO:0102828', 'abnormal occipital region morphology', 0.4107142857142857, 6.272837960958401, 1.6050994245019483, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(629304, 'HP:0030775', 'Modic type vertebral endplate changes', 'XPO:0102272', 'abnormal notochordal sheath morphology', 0.47619047619047616, 4.638757693672553, 1.4862477031377266, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(629305, 'HP:0030775', 'Modic type vertebral endplate changes', 'XPO:0102806', 'abnormal articular system morphology', 0.4878048780487805, 4.638757693672553, 1.5042634845863214, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(629306, 'HP:0030775', 'Modic type vertebral endplate changes', 'XPO:0102113', 'abnormal anatomical line morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(629307, 'HP:0030775', 'Modic type vertebral endplate changes', 'XPO:0102217', 'abnormal elastica externa morphology', 0.5, 4.638757693672553, 1.5229507040072823, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(629308, 'HP:0030775', 'Modic type vertebral endplate changes', 'XPO:0102144', 'abnormal cranial skeleton morphology', 0.45652173913043476, 6.211345574613551, 1.6839282300806968, 'UPHENO:0087089', 'abnormal axial skeleton plus cranial skeleton morphology'),
(629309, 'HP:0030775', 'Modic type vertebral endplate changes', 'XPO:0102567', 'abnormal skeleton morphology', 0.47619047619047616, 4.638757693672553, 1.4862477031377266, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(629310, 'HP:0030775', 'Modic type vertebral endplate changes', 'XPO:0140852', 'abnormally necrotic vertebral centrum', 0.40625, 8.361863005979023, 1.843097079965941, 'UPHENO:0076695', 'abnormal vertebral column morphology'),
(629311, 'HP:0030775', 'Modic type vertebral endplate changes', 'XPO:0140019', 'abnormally necrotic skeletal system', 0.4444444444444444, 4.638757693672553, 1.4358516936218344, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(629312, 'HP:0030775', 'Modic type vertebral endplate changes', 'XPO:0141713', 'increased size of the posterior notochord', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(629313, 'HP:0030775', 'Modic type vertebral endplate changes', 'XPO:0128184', 'decreased size of the skeleton', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(629314, 'HP:0030775', 'Modic type vertebral endplate changes', 'XPO:0102564', 'abnormal olfactory region morphology', 0.40350877192982454, 6.272837960958401, 1.5909573036826314, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(629315, 'HP:0030775', 'Modic type vertebral endplate changes', 'XPO:0103218', 'abnormal joint morphology', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(629316, 'HP:0030775', 'Modic type vertebral endplate changes', 'XPO:0102542', 'abnormal vacuolated notochordal tissue morphology', 0.43478260869565216, 4.638757693672553, 1.4201588541997616, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(629317, 'HP:0030775', 'Modic type vertebral endplate changes', 'XPO:0139998', 'abnormally necrotic axial skeleton', 0.4117647058823529, 6.211345574613551, 1.599253852164941, 'UPHENO:0087089', 'abnormal axial skeleton plus cranial skeleton morphology'),
(629318, 'HP:0030775', 'Modic type vertebral endplate changes', 'XPO:0125260', 'absent vertebral column', 0.46296296296296297, 8.05344015541032, 1.9309180501496346, 'UPHENO:0002813', 'abnormal vertebral column'),
(629319, 'HP:0030775', 'Modic type vertebral endplate changes', 'XPO:0102461', 'abnormal postcranial axial skeleton morphology', 0.5, 6.272837960958401, 1.770993783297728, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(629320, 'HP:0030775', 'Modic type vertebral endplate changes', 'XPO:0102401', 'abnormal neurocranium morphology', 0.40350877192982454, 6.272837960958401, 1.5909573036826314, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(629321, 'HP:0030775', 'Modic type vertebral endplate changes', 'XPO:0129434', 'decreased size of the notochordal sheath', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(629322, 'HP:0030775', 'Modic type vertebral endplate changes', 'XPO:0128227', 'decreased size of the vertebral column', 0.4727272727272727, 8.361863005979023, 1.9881852765111048, 'UPHENO:0076695', 'abnormal vertebral column morphology'),
(629323, 'HP:0030775', 'Modic type vertebral endplate changes', 'XPO:0101858', 'abnormal vertebral element morphology', 0.4727272727272727, 8.361863005979023, 1.9881852765111048, 'UPHENO:0076695', 'abnormal vertebral column morphology'),
(629324, 'HP:0030775', 'Modic type vertebral endplate changes', 'XPO:0101638', 'abnormal anatomical structure morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(629325, 'HP:0030775', 'Modic type vertebral endplate changes', 'XPO:0100693', 'abnormal vertebral centrum', 0.5102040816326531, 8.05344015541032, 2.0270416962841815, 'UPHENO:0002813', 'abnormal vertebral column'),
(629326, 'HP:0030775', 'Modic type vertebral endplate changes', 'XPO:0139771', 'abnormally necrotic skeletal subdivision', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(629327, 'HP:0030775', 'Modic type vertebral endplate changes', 'XPO:0139774', 'abnormally necrotic elastica externa', 0.4444444444444444, 4.638757693672553, 1.4358516936218344, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(629328, 'HP:0030775', 'Modic type vertebral endplate changes', 'XPO:0102351', 'abnormal sphenoid region morphology', 0.40350877192982454, 6.272837960958401, 1.5909573036826314, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(629329, 'HP:0030775', 'Modic type vertebral endplate changes', 'XPO:0103116', 'abnormal bone marrow morphology', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(629330, 'HP:0030775', 'Modic type vertebral endplate changes', 'XPO:0102728', 'abnormal tendon morphology', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(629331, 'HP:0030775', 'Modic type vertebral endplate changes', 'XPO:0101226', 'abnormal postsacral vertebra', 0.4166666666666667, 8.05344015541032, 1.8318297040812228, 'UPHENO:0002813', 'abnormal vertebral column'),
(629332, 'HP:0030775', 'Modic type vertebral endplate changes', 'XPO:0128890', 'decreased size of the elastica externa', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(629333, 'HP:0030775', 'Modic type vertebral endplate changes', 'XPO:0128580', 'decreased size of the postcranial axial skeleton', 0.42592592592592593, 6.272837960958401, 1.6345532468244968, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(629334, 'HP:0030775', 'Modic type vertebral endplate changes', 'XPO:0141248', 'abnormally necrotic transverse process', 0.4057971014492754, 8.748525470353618, 1.884177878498911, 'HP:0003468', 'Abnormal vertebral morphology'),
(629335, 'HP:0030775', 'Modic type vertebral endplate changes', 'XPO:0102164', 'abnormal mandibular mesenchyme morphology', 0.4117647058823529, 6.211345574613551, 1.599253852164941, 'UPHENO:0087089', 'abnormal axial skeleton plus cranial skeleton morphology'),
(629336, 'HP:0030775', 'Modic type vertebral endplate changes', 'XPO:0102097', 'abnormal skeletal system morphology', 0.5, 4.638757693672553, 1.5229507040072823, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(629337, 'HP:0030775', 'Modic type vertebral endplate changes', 'XPO:0101982', 'abnormal appendicular skeleton morphology', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(629338, 'HP:0030775', 'Modic type vertebral endplate changes', 'XPO:0140559', 'abnormally necrotic articular system', 0.43478260869565216, 4.638757693672553, 1.4201588541997616, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(629339, 'HP:0030775', 'Modic type vertebral endplate changes', 'XPO:0101860', 'abnormal skeletal subdivision morphology', 0.46511627906976744, 4.638757693672553, 1.4688640910537754, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(629340, 'HP:0030775', 'Modic type vertebral endplate changes', 'XPO:0102325', 'abnormal vertebral centrum morphology', 0.4642857142857143, 8.361863005979023, 1.9703536582274415, 'UPHENO:0076695', 'abnormal vertebral column morphology'),
(629341, 'HP:0030775', 'Modic type vertebral endplate changes', 'XPO:0101957', 'abnormal axial skeleton morphology', 0.4666666666666667, 6.211345574613551, 1.702535736723214, 'UPHENO:0087089', 'abnormal axial skeleton plus cranial skeleton morphology'),
(629342, 'HP:0030775', 'Modic type vertebral endplate changes', 'XPO:0100895', 'abnormal presacral vertebra', 0.4166666666666667, 8.05344015541032, 1.8318297040812228, 'UPHENO:0002813', 'abnormal vertebral column'),
(629343, 'HP:0030775', 'Modic type vertebral endplate changes', 'XPO:0129786', 'increased size of the articular system', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(629344, 'HP:0030775', 'Modic type vertebral endplate changes', 'XPO:0140510', 'abnormally necrotic postcranial axial skeleton', 0.4423076923076923, 6.272837960958401, 1.6656903922192745, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(629345, 'HP:0030775', 'Modic type vertebral endplate changes', 'XPO:0101680', 'abnormal skeletal element morphology', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(629346, 'HP:0030775', 'Modic type vertebral endplate changes', 'XPO:0129707', 'increased size of the vertebral column', 0.4727272727272727, 8.361863005979023, 1.9881852765111048, 'UPHENO:0076695', 'abnormal vertebral column morphology'),
(629347, 'HP:0030775', 'Modic type vertebral endplate changes', 'XPO:0102605', 'abnormal dermal skeleton morphology', 0.4444444444444444, 4.638757693672553, 1.4358516936218344, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(629348, 'HP:0030775', 'Modic type vertebral endplate changes', 'XPO:0141723', 'abnormal posterior notochord morphology', 0.47619047619047616, 4.638757693672553, 1.4862477031377266, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(629349, 'HP:0030775', 'Modic type vertebral endplate changes', 'XPO:0100584', 'abnormal vertebral column', 0.5952380952380952, 8.05344015541032, 2.1894552697464333, 'UPHENO:0002813', 'abnormal vertebral column'),
(629350, 'HP:0030775', 'Modic type vertebral endplate changes', 'XPO:0129832', 'increased size of the skeletal system', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(629351, 'HP:0030775', 'Modic type vertebral endplate changes', 'XPO:0139917', 'abnormally necrotic notochord', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(629352, 'HP:0030775', 'Modic type vertebral endplate changes', 'XPO:0100252', 'abnormal caudal vertebra', 0.4032258064516129, 8.05344015541032, 1.8020418700394085, 'UPHENO:0002813', 'abnormal vertebral column'),
(629353, 'HP:0030775', 'Modic type vertebral endplate changes', 'XPO:0101976', 'abnormal portion of organism substance morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(629354, 'HP:0030775', 'Modic type vertebral endplate changes', 'XPO:0126787', 'abnormally localised vertebral centrum', 0.4166666666666667, 8.05344015541032, 1.8318297040812228, 'UPHENO:0002813', 'abnormal vertebral column'),
(629355, 'HP:0030775', 'Modic type vertebral endplate changes', 'XPO:0141704', 'decreased size of the anterior notochord', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(629356, 'HP:0030775', 'Modic type vertebral endplate changes', 'XPO:0102980', 'abnormal perichordal tissue morphology', 0.43478260869565216, 4.638757693672553, 1.4201588541997616, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(629357, 'HP:0030775', 'Modic type vertebral endplate changes', 'XPO:0140103', 'abnormally necrotic vertebral column', 0.49056603773584906, 8.361863005979023, 2.025350834530429, 'UPHENO:0076695', 'abnormal vertebral column morphology'),
(629358, 'HP:0030775', 'Modic type vertebral endplate changes', 'XPO:0128352', 'decreased size of the skeletal system', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(629359, 'HP:0030775', 'Modic type vertebral endplate changes', 'XPO:0107372', 'abnormal flexural organ morphology', 0.47619047619047616, 4.638757693672553, 1.4862477031377266, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(629360, 'HP:0030775', 'Modic type vertebral endplate changes', 'XPO:0140432', 'abnormally necrotic skeleton', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(629361, 'HP:0030775', 'Modic type vertebral endplate changes', 'XPO:0140350', 'abnormally necrotic notochordal sheath', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(629362, 'HP:0030775', 'Modic type vertebral endplate changes', 'XPO:0141709', 'increased size of the anterior notochord', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(629363, 'HP:0030775', 'Modic type vertebral endplate changes', 'XPO:0140043', 'abnormally necrotic perichondrium', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(629364, 'HP:0030775', 'Modic type vertebral endplate changes', 'XPO:0141719', 'abnormal anterior notochord morphology', 0.47619047619047616, 4.638757693672553, 1.4862477031377266, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(629365, 'HP:0030775', 'Modic type vertebral endplate changes', 'XPO:0130188', 'increased size of the flexural organ', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(629366, 'HP:0030775', 'Modic type vertebral endplate changes', 'XPO:0139795', 'abnormally necrotic vertebral element', 0.4126984126984127, 8.361863005979023, 1.8576672440911264, 'UPHENO:0076695', 'abnormal vertebral column morphology'),
(629367, 'HP:0030775', 'Modic type vertebral endplate changes', 'XPO:0102010', 'abnormal perichondrium morphology', 0.46511627906976744, 4.638757693672553, 1.4688640910537754, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(629368, 'HP:0030775', 'Modic type vertebral endplate changes', 'XPO:0129664', 'increased size of the skeleton', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(629369, 'HP:0030775', 'Modic type vertebral endplate changes', 'XPO:0130368', 'increased size of the elastica externa', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(629370, 'HP:0030775', 'Modic type vertebral endplate changes', 'XPO:0101070', 'abnormal rib', 0.4098360655737705, 8.05344015541032, 1.816752660002781, 'UPHENO:0002813', 'abnormal vertebral column'),
(629371, 'HP:0030775', 'Modic type vertebral endplate changes', 'XPO:0103152', 'abnormal otic region morphology', 0.40350877192982454, 6.272837960958401, 1.5909573036826314, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(629372, 'HP:0030775', 'Modic type vertebral endplate changes', 'XPO:0126886', 'abnormally localised vertebral column', 0.49019607843137253, 8.05344015541032, 1.9868982817607654, 'UPHENO:0002813', 'abnormal vertebral column'),
(629373, 'HP:0030775', 'Modic type vertebral endplate changes', 'XPO:0140683', 'abnormally necrotic flexural organ', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(629374, 'HP:0030775', 'Modic type vertebral endplate changes', 'XPO:0102054', 'abnormal notochord morphology', 0.47619047619047616, 4.638757693672553, 1.4862477031377266, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(629375, 'HP:0030775', 'Modic type vertebral endplate changes', 'XPO:0100927', 'abnormal sacral vertebra', 0.4166666666666667, 8.05344015541032, 1.8318297040812228, 'UPHENO:0002813', 'abnormal vertebral column'),
(629376, 'HP:0030775', 'Modic type vertebral endplate changes', 'XPO:0101446', 'abnormal transverse process', 0.4098360655737705, 8.05344015541032, 1.816752660002781, 'UPHENO:0002813', 'abnormal vertebral column'),
(629377, 'HP:0030775', 'Modic type vertebral endplate changes', 'XPO:0102216', 'abnormal vertebral column morphology', 0.5531914893617021, 8.361863005979023, 2.15074671919221, 'UPHENO:0076695', 'abnormal vertebral column morphology'),
(629378, 'HP:0030775', 'Modic type vertebral endplate changes', 'XPO:0128709', 'decreased size of the flexural organ', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(629379, 'HP:0025245', 'Cutaneous cyst', 'XPO:0101241', 'abnormal nucleate erythrocyte', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(629380, 'HP:0025245', 'Cutaneous cyst', 'XPO:0101535', 'abnormal absorptive cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(629381, 'HP:0025245', 'Cutaneous cyst', 'XPO:0101014', 'abnormal goblet cell', 0.40540540540540543, 6.8660902472206855, 1.6683974647021622, 'HP:0000951', 'Abnormality of the skin'),
(629382, 'HP:0025245', 'Cutaneous cyst', 'XPO:0100983', 'abnormal skin gland', 0.4838709677419355, 6.8660902472206855, 1.8227182263109507, 'HP:0000951', 'Abnormality of the skin'),
(629383, 'HP:0025245', 'Cutaneous cyst', 'XPO:0100791', 'abnormal multiciliated cell precursor', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(629384, 'HP:0025245', 'Cutaneous cyst', 'XPO:0102139', 'abnormal skin morphology', 0.46153846153846156, 7.420886955069779, 1.8506822386605823, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(629385, 'HP:0025245', 'Cutaneous cyst', 'XPO:0100477', 'abnormal pericyte', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(629386, 'HP:0025245', 'Cutaneous cyst', 'XPO:0103223', 'abnormal xanthophore morphology', 0.4090909090909091, 7.420886955069779, 1.7423597190908553, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(629387, 'HP:0025245', 'Cutaneous cyst', 'XPO:0100344', 'abnormal portion of organism substance', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(629388, 'HP:0025245', 'Cutaneous cyst', 'XPO:0100481', 'abnormal anatomical line', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(629389, 'HP:0025245', 'Cutaneous cyst', 'XPO:0101448', 'abnormal myelin accumulating cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(629390, 'HP:0025245', 'Cutaneous cyst', 'XPO:0102840', 'abnormal stratum spongiosum morphology', 0.42857142857142855, 7.420886955069779, 1.7833620281931915, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(629391, 'HP:0025245', 'Cutaneous cyst', 'XPO:0101278', 'abnormal pigment cell', 0.4411764705882353, 6.8660902472206855, 1.740447489012273, 'HP:0000951', 'Abnormality of the skin'),
(629392, 'HP:0025245', 'Cutaneous cyst', 'XPO:0100802', 'abnormal exocrine cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(629393, 'HP:0025245', 'Cutaneous cyst', 'XPO:0102945', 'abnormal Eberth-Kastschenko layer morphology', 0.42857142857142855, 7.420886955069779, 1.7833620281931915, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(629394, 'HP:0025245', 'Cutaneous cyst', 'XPO:0100006', 'abnormal anatomical structure', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(629395, 'HP:0025245', 'Cutaneous cyst', 'XPO:0101373', 'abnormal oxygen accumulating cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(629396, 'HP:0025245', 'Cutaneous cyst', 'XPO:0101132', 'abnormal apoptotic cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(629397, 'HP:0025245', 'Cutaneous cyst', 'XPO:0100108', 'abnormal cell part', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(629398, 'HP:0025245', 'Cutaneous cyst', 'XPO:0101208', 'abnormal stratum spongiosum', 0.4411764705882353, 6.8660902472206855, 1.740447489012273, 'HP:0000951', 'Abnormality of the skin'),
(629399, 'HP:0025245', 'Cutaneous cyst', 'XPO:0100704', 'abnormal Merkel cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(629400, 'HP:0025245', 'Cutaneous cyst', 'XPO:0100929', 'abnormal dermis', 0.46875, 6.8660902472206855, 1.7940122082596586, 'HP:0000951', 'Abnormality of the skin'),
(629401, 'HP:0025245', 'Cutaneous cyst', 'XPO:0101333', 'abnormal barrier epithelial cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(629402, 'HP:0025245', 'Cutaneous cyst', 'XPO:0102727', 'abnormal skin seromucous gland morphology', 0.43902439024390244, 7.420886955069779, 1.8049793268950312, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(629403, 'HP:0025245', 'Cutaneous cyst', 'XPO:0100289', 'abnormal chondroblast', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(629404, 'HP:0025245', 'Cutaneous cyst', 'XPO:0100081', 'abnormal anatomical entity in vitro', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(629405, 'HP:0025245', 'Cutaneous cyst', 'XPO:0101591', 'abnormal xanthophore', 0.42857142857142855, 6.8660902472206855, 1.7154037734456928, 'HP:0000951', 'Abnormality of the skin'),
(629406, 'HP:0025245', 'Cutaneous cyst', 'XPO:0101529', 'abnormal skin mucous gland', 0.4411764705882353, 6.8660902472206855, 1.740447489012273, 'HP:0000951', 'Abnormality of the skin'),
(629407, 'HP:0025245', 'Cutaneous cyst', 'XPO:0100285', 'abnormal progenitor cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(629408, 'HP:0025245', 'Cutaneous cyst', 'XPO:0101095', 'abnormal skin seromucous gland', 0.46875, 6.8660902472206855, 1.7940122082596586, 'HP:0000951', 'Abnormality of the skin'),
(629409, 'HP:0025245', 'Cutaneous cyst', 'XPO:0101515', 'abnormal neuromast mantle cell', 0.4411764705882353, 6.8660902472206855, 1.740447489012273, 'HP:0000951', 'Abnormality of the skin'),
(629410, 'HP:0025245', 'Cutaneous cyst', 'XPO:0100852', 'abnormal interdigital region', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(629411, 'HP:0025245', 'Cutaneous cyst', 'XPO:0102910', 'abnormal pigment cell morphology', 0.42857142857142855, 7.420886955069779, 1.7833620281931915, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(629412, 'HP:0025245', 'Cutaneous cyst', 'XPO:0100172', 'abnormal stem cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(629413, 'HP:0025245', 'Cutaneous cyst', 'XPO:0101237', 'abnormal mucus secreting cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(629414, 'HP:0025245', 'Cutaneous cyst', 'XPO:0101322', 'abnormal iridophore', 0.42857142857142855, 6.8660902472206855, 1.7154037734456928, 'HP:0000951', 'Abnormality of the skin'),
(629415, 'HP:0025245', 'Cutaneous cyst', 'XPO:0102561', 'abnormal dermis morphology', 0.45, 7.420886955069779, 1.8274022900777487, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(629416, 'HP:0025245', 'Cutaneous cyst', 'XPO:0100994', 'abnormal granular gland', 0.46875, 6.8660902472206855, 1.7940122082596586, 'HP:0000951', 'Abnormality of the skin'),
(629417, 'HP:0025245', 'Cutaneous cyst', 'XPO:0102615', 'abnormal skin gland morphology', 0.46153846153846156, 7.420886955069779, 1.8506822386605823, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(629418, 'HP:0025245', 'Cutaneous cyst', 'XPO:0100533', 'abnormal melanoblast', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(629419, 'HP:0025245', 'Cutaneous cyst', 'XPO:0100004', 'abnormal cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(629420, 'HP:0025245', 'Cutaneous cyst', 'XPO:0100754', 'abnormal electrically active cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(629421, 'HP:0025245', 'Cutaneous cyst', 'XPO:0100691', 'abnormal keratin accumulating cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(629422, 'HP:0025245', 'Cutaneous cyst', 'XPO:0102886', 'abnormal stratum compactum morphology', 0.42857142857142855, 7.420886955069779, 1.7833620281931915, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(629423, 'HP:0025245', 'Cutaneous cyst', 'XPO:0101435', 'abnormal paracrine cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(629424, 'HP:0025245', 'Cutaneous cyst', 'XPO:0103019', 'abnormal melanophore morphology', 0.4090909090909091, 7.420886955069779, 1.7423597190908553, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(629425, 'HP:0025245', 'Cutaneous cyst', 'XPO:0102626', 'abnormal granular gland morphology', 0.43902439024390244, 7.420886955069779, 1.8049793268950312, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(629426, 'HP:0025245', 'Cutaneous cyst', 'XPO:0101297', 'abnormal barrier cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(629427, 'HP:0025245', 'Cutaneous cyst', 'XPO:0102176', 'abnormal neuromast support cell morphology', 0.42857142857142855, 7.420886955069779, 1.7833620281931915, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(629428, 'HP:0025245', 'Cutaneous cyst', 'XPO:0100549', 'abnormal mitotic cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(629429, 'HP:0025245', 'Cutaneous cyst', 'XPO:0100026', 'abnormal germ cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(629430, 'HP:0025245', 'Cutaneous cyst', 'XPO:0100544', 'abnormal neuromast support cell', 0.4411764705882353, 6.8660902472206855, 1.740447489012273, 'HP:0000951', 'Abnormality of the skin'),
(629431, 'HP:0025245', 'Cutaneous cyst', 'XPO:0100337', 'abnormal zygote', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(629432, 'HP:0025245', 'Cutaneous cyst', 'XPO:0101387', 'abnormal melanophore', 0.42857142857142855, 6.8660902472206855, 1.7154037734456928, 'HP:0000951', 'Abnormality of the skin'),
(629433, 'HP:0025245', 'Cutaneous cyst', 'XPO:0101467', 'abnormal alkali secreting cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(629434, 'HP:0025245', 'Cutaneous cyst', 'XPO:0100715', 'abnormal ciliated cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(629435, 'HP:0025245', 'Cutaneous cyst', 'XPO:0101004', 'abnormal acid secreting cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(629436, 'HP:0025245', 'Cutaneous cyst', 'XPO:0101254', 'abnormal stratum compactum', 0.4411764705882353, 6.8660902472206855, 1.740447489012273, 'HP:0000951', 'Abnormality of the skin'),
(629437, 'HP:0025245', 'Cutaneous cyst', 'XPO:0102954', 'abnormal iridophore morphology', 0.4090909090909091, 7.420886955069779, 1.7423597190908553, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(629438, 'HP:0025245', 'Cutaneous cyst', 'XPO:0100638', 'abnormal polar body', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(629439, 'HP:0025245', 'Cutaneous cyst', 'XPO:0101326', 'abnormal cementoblast', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(629440, 'HP:0025245', 'Cutaneous cyst', 'XPO:0100507', 'abnormal skin', 0.5, 6.8660902472206855, 1.8528478414619864, 'HP:0000951', 'Abnormality of the skin'),
(629441, 'HP:0025245', 'Cutaneous cyst', 'XPO:0100653', 'abnormal myoblast', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(629442, 'HP:0025245', 'Cutaneous cyst', 'XPO:0101313', 'abnormal Eberth-Kastschenko layer', 0.4411764705882353, 6.8660902472206855, 1.740447489012273, 'HP:0000951', 'Abnormality of the skin'),
(629443, 'HP:0025245', 'Cutaneous cyst', 'XPO:0103147', 'abnormal neuromast mantle cell morphology', 0.42857142857142855, 7.420886955069779, 1.7833620281931915, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(629444, 'HP:0009694', 'Small thumb epiphysis', 'XPO:0103432', 'decreased size of the forelimb digit', 0.4146341463414634, 9.84136243681758, 2.0200408195941986, 'UPHENO:0012274', 'decreased size of the anatomical entity in the pectoral complex'),
(629445, 'HP:0009694', 'Small thumb epiphysis', 'XPO:0102214', 'abnormal forelimb digit morphology', 0.4051724137931034, 7.492661022682715, 1.7423603393941962, 'HP:0001167', 'Abnormal finger morphology'),
(629446, 'HP:0009694', 'Small thumb epiphysis', 'XPO:0103609', 'abnormally increased number of forelimb digit in the regenerating forelimb', 0.4222222222222222, 7.774297771301195, 1.811761927300621, 'HP:0005918', 'Abnormal finger phalanx morphology'),
(629447, 'HP:0009694', 'Small thumb epiphysis', 'XPO:0129148', 'decreased size of the forelimb digit 4', 0.40476190476190477, 9.84136243681758, 1.995847841239042, 'UPHENO:0012274', 'decreased size of the anatomical entity in the pectoral complex'),
(629448, 'HP:0009694', 'Small thumb epiphysis', 'XPO:0128172', 'decreased size of the forelimb digit 3', 0.40476190476190477, 9.84136243681758, 1.995847841239042, 'UPHENO:0012274', 'decreased size of the anatomical entity in the pectoral complex'),
(629449, 'HP:0009694', 'Small thumb epiphysis', 'XPO:0115786', 'duplicated forelimb digit 2 in regenerating forelimb', 0.40714285714285714, 7.774297771301195, 1.7791148942344661, 'HP:0005918', 'Abnormal finger phalanx morphology'),
(629450, 'HP:0009694', 'Small thumb epiphysis', 'XPO:0115787', 'duplicated forelimb digit 3 in regenerating forelimb', 0.40714285714285714, 7.774297771301195, 1.7791148942344661, 'HP:0005918', 'Abnormal finger phalanx morphology'),
(629451, 'HP:0009694', 'Small thumb epiphysis', 'XPO:0115788', 'duplicated forelimb digit 4 in regenerating forelimb', 0.40714285714285714, 7.774297771301195, 1.7791148942344661, 'HP:0005918', 'Abnormal finger phalanx morphology'),
(629452, 'HP:0009694', 'Small thumb epiphysis', 'XPO:0129188', 'decreased size of the forelimb digit 2', 0.40476190476190477, 9.84136243681758, 1.995847841239042, 'UPHENO:0012274', 'decreased size of the anatomical entity in the pectoral complex'),
(629453, 'HP:0009694', 'Small thumb epiphysis', 'XPO:0129161', 'decreased size of the forelimb digit 5', 0.40476190476190477, 9.84136243681758, 1.995847841239042, 'UPHENO:0012274', 'decreased size of the anatomical entity in the pectoral complex'),
(629454, 'HP:0009694', 'Small thumb epiphysis', 'XPO:0115789', 'duplicated forelimb digit 5 in regenerating forelimb', 0.40714285714285714, 7.774297771301195, 1.7791148942344661, 'HP:0005918', 'Abnormal finger phalanx morphology'),
(629455, 'HP:0009694', 'Small thumb epiphysis', 'XPO:0103634', 'abnormally increased number of forelimb digit', 0.4418604651162791, 7.774297771301195, 1.8534170683307085, 'HP:0005918', 'Abnormal finger phalanx morphology'),
(629456, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0115407', 'multiple pancreases', 0.45714285714285713, 7.1173123385767045, 1.8037817211722333, 'HP:0002012', 'Abnormality of the abdominal organs'),
(629457, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0141748', 'abnormal gas homeostasis', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(629458, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0142054', 'abnormal digestive tract', 0.625, 5.05060299610679, 1.7766898639230044, 'HP:0025031', 'Abnormality of the digestive system'),
(629459, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100062', 'abnormal anatomical space', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(629460, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0101212', 'abnormal glomeral mesenchyme', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(629461, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100599', 'abnormal adult immune system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(629462, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100423', 'abnormal process', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(629463, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0107285', 'abnormal flexural organ', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(629464, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0126520', 'abnormally localised hindgut', 0.45454545454545453, 5.05060299610679, 1.5151662069205463, 'HP:0025031', 'Abnormality of the digestive system'),
(629465, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0131685', 'abnormal cortical actin cytoskeleton', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(629466, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0101241', 'abnormal nucleate erythrocyte', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(629467, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0107304', 'abnormal hindgut endoderm', 0.5357142857142857, 5.05060299610679, 1.6448951870820767, 'HP:0025031', 'Abnormality of the digestive system'),
(629468, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0141714', 'abnormal anterior notochord', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(629469, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0101366', 'abnormal morula cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(629470, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0141797', 'abnormal hydrogen metabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(629471, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0101200', 'abnormal joint region', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(629472, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0107305', 'abnormal dorsal posterior hindgut endoderm', 0.5, 5.05060299610679, 1.5891197242666757, 'HP:0025031', 'Abnormality of the digestive system'),
(629473, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0139906', 'abnormally necrotic alimentary system', 0.40540540540540543, 5.05060299610679, 1.4309233924911664, 'HP:0025031', 'Abnormality of the digestive system'),
(629474, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100486', 'abnormal oral evagination', 0.6, 5.05060299610679, 1.740793439114496, 'HP:0025031', 'Abnormality of the digestive system'),
(629475, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0101103', 'abnormal pharyngeal mesenchyme', 0.4838709677419355, 5.05060299610679, 1.5632786569919361, 'HP:0025031', 'Abnormality of the digestive system'),
(629476, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100638', 'abnormal polar body', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(629477, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0131421', 'abnormally increased number of cilium in the alimentary system', 0.42857142857142855, 5.05060299610679, 1.471238981671103, 'HP:0025031', 'Abnormality of the digestive system'),
(629478, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100265', 'abnormal sensory epithelial cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(629479, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0101040', 'abnormal axial mesoderm', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(629480, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100135', 'abnormal surface structure', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(629481, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0107259', 'abnormal animal-vegetal axis', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(629482, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100626', 'abnormal primordial germ cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(629483, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100152', 'abnormal alimentary system', 0.6818181818181818, 5.05060299610679, 1.855692041231786, 'HP:0025031', 'Abnormality of the digestive system'),
(629484, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0115509', 'abnormally semi-viable whole organism', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(629485, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0142061', 'abnormal digestive tract morphology', 0.4411764705882353, 5.05060299610679, 1.4927180591674907, 'HP:0025031', 'Abnormality of the digestive system'),
(629486, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0101389', 'abnormal wedge region', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(629487, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100888', 'abnormal microtubule', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(629488, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0141271', 'increased surface breathing', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(629489, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0126608', 'abnormally localised foregut', 0.45454545454545453, 5.05060299610679, 1.5151662069205463, 'HP:0025031', 'Abnormality of the digestive system'),
(629490, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100999', 'abnormal serous membrane', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(629491, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100427', 'abnormal olfactory system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(629492, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100232', 'abnormal lymphatic system', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(629493, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100289', 'abnormal chondroblast', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(629494, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100852', 'abnormal interdigital region', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(629495, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0131667', 'abnormal actin cytoskeleton', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(629496, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0107339', 'abnormal yolk platelet', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(629497, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100511', 'abnormal stylopod', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(629498, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0141786', 'abnormal pigment metabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(629499, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0101221', 'abnormal larval immune system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(629500, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100151', 'abnormal primordium', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(629501, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100728', 'abnormal cell condensation', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(629502, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0101078', 'abnormal mucous gland', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(629503, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100794', 'abnormal liver', 0.42105263157894735, 7.1173123385767045, 1.731116139930257, 'HP:0002012', 'Abnormality of the abdominal organs'),
(629504, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0126499', 'abnormally localised liver and biliary system', 0.46875, 5.05060299610679, 1.5386585568036393, 'HP:0025031', 'Abnormality of the digestive system'),
(629505, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0101113', 'abnormal stage IV oocyte', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(629506, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100215', 'abnormal first pancreatic bud', 0.5357142857142857, 5.05060299610679, 1.6448951870820767, 'HP:0025031', 'Abnormality of the digestive system'),
(629507, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100573', 'abnormal extraembryonic structure', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(629508, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0107307', 'abnormal posterior hindgut endoderm', 0.5172413793103449, 5.05060299610679, 1.6162861318637973, 'HP:0025031', 'Abnormality of the digestive system'),
(629509, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0101021', 'abnormal dorsal foregut', 0.5769230769230769, 5.05060299610679, 1.706988406765213, 'HP:0025031', 'Abnormality of the digestive system'),
(629510, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0101264', 'abnormal mitotic spindle', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(629511, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100546', 'abnormal whole organism', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(629512, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100501', 'abnormal urogenital system', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(629513, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100172', 'abnormal stem cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(629514, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100293', 'abnormal duct', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(629515, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100524', 'abnormal intestine', 0.4166666666666667, 5.05060299610679, 1.45066119926208, 'HP:0025031', 'Abnormality of the digestive system'),
(629516, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100642', 'abnormal gustatory system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(629517, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100188', 'abnormal delta cell', 0.4838709677419355, 5.05060299610679, 1.5632786569919361, 'HP:0025031', 'Abnormality of the digestive system'),
(629518, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0101121', 'abnormal Rathkes pouch', 0.4166666666666667, 5.05060299610679, 1.45066119926208, 'HP:0025031', 'Abnormality of the digestive system'),
(629519, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0125342', 'absent gut epithelium', 0.40540540540540543, 5.05060299610679, 1.4309233924911664, 'HP:0025031', 'Abnormality of the digestive system'),
(629520, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0141772', 'abnormal water homeostasis', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(629521, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0101176', 'abnormal non-ciliated epithelial cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(629522, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100205', 'abnormal limb segment', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(629523, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0101575', 'abnormal vitelline membrane', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(629524, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100162', 'abnormal presumptive rhombomere', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(629525, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0101519', 'abnormal hypobranchial placode', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(629526, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100823', 'abnormal blood', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(629527, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0126837', 'abnormally localised midgut', 0.45454545454545453, 5.05060299610679, 1.5151662069205463, 'HP:0025031', 'Abnormality of the digestive system'),
(629528, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0141745', 'abnormal creatinine homeostasis', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(629529, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0107306', 'abnormal ventral posterior hindgut endoderm', 0.5, 5.05060299610679, 1.5891197242666757, 'HP:0025031', 'Abnormality of the digestive system'),
(629530, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100009', 'abnormal multi-tissue structure', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(629531, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100216', 'abnormal hepato-pancreatic progenitor cell', 0.5, 5.05060299610679, 1.5891197242666757, 'HP:0025031', 'Abnormality of the digestive system'),
(629532, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100608', 'abnormal pancreas', 0.47058823529411764, 7.1173123385767045, 1.830115694006218, 'HP:0002012', 'Abnormality of the abdominal organs'),
(629533, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0102118', 'abnormal oral evagination morphology', 0.42857142857142855, 5.05060299610679, 1.471238981671103, 'HP:0025031', 'Abnormality of the digestive system'),
(629534, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0107264', 'abnormal anterior side', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(629535, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100547', 'abnormal blastomere V2', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(629536, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0101141', 'abnormal Keller explant', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(629537, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100549', 'abnormal mitotic cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(629538, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0102618', 'abnormal gut epithelium morphology', 0.40540540540540543, 5.05060299610679, 1.4309233924911664, 'HP:0025031', 'Abnormality of the digestive system'),
(629539, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100621', 'abnormal peritoneum', 0.5357142857142857, 5.05060299610679, 1.6448951870820767, 'HP:0025031', 'Abnormality of the digestive system'),
(629540, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0127393', 'abnormally localised pharyngeal cavity', 0.4838709677419355, 5.05060299610679, 1.5632786569919361, 'HP:0025031', 'Abnormality of the digestive system'),
(629541, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100784', 'abnormal left blastomere', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(629542, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0115391', 'abnormally undifferentiated alimentary system', 0.6521739130434783, 5.05060299610679, 1.814902619756796, 'HP:0025031', 'Abnormality of the digestive system'),
(629543, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100014', 'abnormal tissue', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(629544, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100362', 'abnormal acinar cell', 0.42105263157894735, 7.1173123385767045, 1.731116139930257, 'HP:0002012', 'Abnormality of the abdominal organs'),
(629545, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0141778', 'abnormal biosynthetic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(629546, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100462', 'abnormal anterior foregut', 0.5769230769230769, 5.05060299610679, 1.706988406765213, 'HP:0025031', 'Abnormality of the digestive system'),
(629547, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0131673', 'abnormal buccopharyngeal membrane', 0.4838709677419355, 5.05060299610679, 1.5632786569919361, 'HP:0025031', 'Abnormality of the digestive system'),
(629548, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100842', 'abnormal left-dorsal blastomere', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(629549, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0116494', 'absent biological process', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(629550, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0101409', 'abnormal perivitelline space', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(629551, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0126176', 'absent dorsal foregut', 0.42857142857142855, 5.05060299610679, 1.471238981671103, 'HP:0025031', 'Abnormality of the digestive system'),
(629552, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0101157', 'abnormal female organism', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(629553, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0131683', 'abnormal stomach epithelium', 0.5, 5.05060299610679, 1.5891197242666757, 'HP:0025031', 'Abnormality of the digestive system'),
(629554, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0101198', 'abnormal digestive enzyme secreting cell', 0.5357142857142857, 5.05060299610679, 1.6448951870820767, 'HP:0025031', 'Abnormality of the digestive system'),
(629555, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0107284', 'abnormal migrating myoblast', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(629556, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0101381', 'abnormal ventral foregut', 0.5769230769230769, 5.05060299610679, 1.706988406765213, 'HP:0025031', 'Abnormality of the digestive system'),
(629557, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0101168', 'abnormal circulating cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(629558, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0131682', 'abnormal esophageal epithelium', 0.4166666666666667, 5.05060299610679, 1.45066119926208, 'HP:0025031', 'Abnormality of the digestive system'),
(629559, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100164', 'abnormal neural nucleus', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(629560, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100913', 'abnormal Brachets cleft', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(629561, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0101498', 'abnormal stage II oocyte', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(629562, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0115758', 'abnormally decreased mobility of melanoblast', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(629563, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100417', 'abnormal dense regular connective tissue', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(629564, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0141833', 'edematous alimentary system', 0.4411764705882353, 5.05060299610679, 1.4927180591674907, 'HP:0025031', 'Abnormality of the digestive system'),
(629565, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0101472', 'abnormal zygote cortex', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(629566, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100890', 'abnormal pharyngeal cavity', 0.625, 5.05060299610679, 1.7766898639230044, 'HP:0025031', 'Abnormality of the digestive system'),
(629567, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0101461', 'abnormal sperm entry point', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(629568, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0115495', 'abnormally protruding proctodeum', 0.5, 5.05060299610679, 1.5891197242666757, 'HP:0025031', 'Abnormality of the digestive system'),
(629569, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0107265', 'abnormal posterior side', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(629570, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0127495', 'abnormally localised proctodeum', 0.40540540540540543, 5.05060299610679, 1.4309233924911664, 'HP:0025031', 'Abnormality of the digestive system'),
(629571, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100295', 'abnormal extracellular matrix', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(629572, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0101326', 'abnormal cementoblast', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(629573, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0124857', 'absent alimentary system', 0.46875, 5.05060299610679, 1.5386585568036393, 'HP:0025031', 'Abnormality of the digestive system'),
(629574, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0131691', 'abnormal molecular function', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(629575, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0101333', 'abnormal barrier epithelial cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(629576, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100629', 'abnormal branchial arch 2', 0.46875, 5.05060299610679, 1.5386585568036393, 'HP:0025031', 'Abnormality of the digestive system'),
(629577, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100454', 'abnormal lung bud', 0.4838709677419355, 5.05060299610679, 1.5632786569919361, 'HP:0025031', 'Abnormality of the digestive system'),
(629578, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100282', 'abnormal pelvic girdle primordium', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(629579, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100786', 'abnormal presumptive axial mesoderm', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(629580, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100239', 'abnormal acellular anatomical structure', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(629581, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0101174', 'abnormal articular system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(629582, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100721', 'abnormal centromere', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(629583, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100258', 'abnormal organ part', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(629584, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0103013', 'abnormal ventral foregut morphology', 0.40540540540540543, 5.05060299610679, 1.4309233924911664, 'HP:0025031', 'Abnormality of the digestive system'),
(629585, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100991', 'abnormal iliac process primordium', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(629586, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0141781', 'abnormal secondary metabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(629587, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0101535', 'abnormal absorptive cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(629588, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100429', 'abnormal spermatid', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(629589, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0107260', 'abnormal anterior-posterior axis', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(629590, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0102125', 'abnormal liver and biliary system morphology', 0.4411764705882353, 5.05060299610679, 1.4927180591674907, 'HP:0025031', 'Abnormality of the digestive system'),
(629591, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100081', 'abnormal anatomical entity in vitro', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(629592, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0101072', 'abnormal mitochondrial cloud', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(629593, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100704', 'abnormal Merkel cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(629594, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100788', 'abnormal branchial arch 4', 0.46875, 5.05060299610679, 1.5386585568036393, 'HP:0025031', 'Abnormality of the digestive system'),
(629595, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0101784', 'abnormal alimentary system morphology', 0.46875, 5.05060299610679, 1.5386585568036393, 'HP:0025031', 'Abnormality of the digestive system'),
(629596, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100903', 'abnormal dorsal pancreatic bud', 0.46875, 5.05060299610679, 1.5386585568036393, 'HP:0025031', 'Abnormality of the digestive system'),
(629597, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0101096', 'abnormal tendon', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(629598, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0141792', 'abnormal small molecule metabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(629599, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100494', 'abnormal liver diverticulum', 0.4838709677419355, 5.05060299610679, 1.5632786569919361, 'HP:0025031', 'Abnormality of the digestive system'),
(629600, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0101378', 'abnormal blastomere D1', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(629601, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100069', 'abnormal urinary system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(629602, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100070', 'abnormal anatomical system', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(629603, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0141775', 'abnormal nitrogen compound metabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(629604, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100781', 'abnormal presumptive ectoderm', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(629605, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0141620', 'metaplastic pancreas', 0.43243243243243246, 7.1173123385767045, 1.7543536379396512, 'HP:0002012', 'Abnormality of the abdominal organs'),
(629606, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0102653', 'abnormal dorsal foregut morphology', 0.40540540540540543, 5.05060299610679, 1.4309233924911664, 'HP:0025031', 'Abnormality of the digestive system'),
(629607, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0102155', 'abnormal midgut morphology', 0.4166666666666667, 5.05060299610679, 1.45066119926208, 'HP:0025031', 'Abnormality of the digestive system'),
(629608, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0141771', 'abnormal urea homeostasis', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(629609, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:00000000', 'Xenopus phenotype', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(629610, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100797', 'abnormal esophagus', 0.46875, 5.05060299610679, 1.5386585568036393, 'HP:0025031', 'Abnormality of the digestive system'),
(629611, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100688', 'abnormal adipose tissue', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(629612, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0124907', 'absent hindgut', 0.42857142857142855, 5.05060299610679, 1.471238981671103, 'HP:0025031', 'Abnormality of the digestive system'),
(629613, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0142052', 'abnormal nasal region', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(629614, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0107266', 'abnormal dorsal side', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(629615, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0101061', 'abnormal plasma membrane', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(629616, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0101193', 'abnormal bile duct', 0.45714285714285713, 7.1173123385767045, 1.8037817211722333, 'HP:0002012', 'Abnormality of the abdominal organs'),
(629617, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100251', 'abnormal proteinaceous extracellular matrix', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(629618, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0101332', 'abnormal left spleen primordium', 0.4411764705882353, 5.05060299610679, 1.4927180591674907, 'HP:0025031', 'Abnormality of the digestive system'),
(629619, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0116434', 'abnormal biological process', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(629620, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100807', 'abnormal matrix-based tissue', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(629621, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100422', 'abnormal notochord', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(629622, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0101451', 'abnormal dorsal lymph space', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(629623, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100579', 'abnormal biliary tree', 0.47058823529411764, 7.1173123385767045, 1.830115694006218, 'HP:0002012', 'Abnormality of the abdominal organs'),
(629624, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0124818', 'absent posterior foregut', 0.42857142857142855, 5.05060299610679, 1.471238981671103, 'HP:0025031', 'Abnormality of the digestive system'),
(629625, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0141904', 'abnormal glucosamine metabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(629626, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100492', 'abnormal gall bladder primordium', 0.5357142857142857, 5.05060299610679, 1.6448951870820767, 'HP:0025031', 'Abnormality of the digestive system'),
(629627, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100557', 'abnormal prime meridian', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(629628, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0107271', 'abnormal apical region', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(629629, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100503', 'abnormal blastomere D2', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(629630, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0126550', 'abnormally localised first pancreatic bud', 0.40540540540540543, 5.05060299610679, 1.4309233924911664, 'HP:0025031', 'Abnormality of the digestive system'),
(629631, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100515', 'abnormal somatic stem cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(629632, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0127173', 'abnormally localised anterior foregut', 0.4411764705882353, 5.05060299610679, 1.4927180591674907, 'HP:0025031', 'Abnormality of the digestive system'),
(629633, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100917', 'abnormal stage III oocyte', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(629634, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0125745', 'absent pharyngeal cavity', 0.46875, 5.05060299610679, 1.5386585568036393, 'HP:0025031', 'Abnormality of the digestive system'),
(629635, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0141263', 'abnormal visually guided collision avoidance behavior', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(629636, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0115505', 'dead whole organism', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(629637, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0107270', 'abnormal proximal-distal axis', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(629638, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100887', 'abnormal right-dorsal blastomere', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(629639, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100915', 'abnormal dermal system', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(629640, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100394', 'abnormal marginal zone', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(629641, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100754', 'abnormal electrically active cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(629642, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0141738', 'abnormal carbon dioxide homeostasis', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(629643, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0115768', 'abnormally abaxially mislocalized anterior foregut', 0.42857142857142855, 5.05060299610679, 1.471238981671103, 'HP:0025031', 'Abnormality of the digestive system'),
(629644, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0141266', 'abnormal surface breathing', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(629645, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0125535', 'absent anterior foregut', 0.42857142857142855, 5.05060299610679, 1.471238981671103, 'HP:0025031', 'Abnormality of the digestive system'),
(629646, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100545', 'abnormal male organism', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(629647, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100006', 'abnormal anatomical structure', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(629648, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100026', 'abnormal germ cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(629649, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100023', 'abnormal mesenchyme', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(629650, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100363', 'abnormal cardiovascular system', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(629651, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0101311', 'abnormal bottle cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(629652, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0101023', 'abnormal ultimobranchial body', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(629653, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100273', 'abnormal visual system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(629654, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100899', 'abnormal secondary spermatogonium', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(629655, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0141787', 'abnormal hormone metabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(629656, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100745', 'abnormal anterior lymph sac', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(629657, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0141276', 'decreased surface breathing', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(629658, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0101570', 'abnormal forelimb region', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(629659, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100130', 'abnormal mouth primordium', 0.5, 5.05060299610679, 1.5891197242666757, 'HP:0025031', 'Abnormality of the digestive system'),
(629660, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100551', 'abnormal oocyte cortex', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(629661, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0142020', 'absent digestive tract', 0.4411764705882353, 5.05060299610679, 1.4927180591674907, 'HP:0025031', 'Abnormality of the digestive system'),
(629662, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0101480', 'abnormal stage V oocyte', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(629663, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100120', 'abnormal genital system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(629664, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0125084', 'absent larval alimentary system', 0.4411764705882353, 5.05060299610679, 1.4927180591674907, 'HP:0025031', 'Abnormality of the digestive system'),
(629665, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0107261', 'abnormal dorsal-ventral axis', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(629666, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0107276', 'abnormal dorsal region', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(629667, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0101362', 'abnormal vegetal cortex', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(629668, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0101110', 'abnormal cell-free extract', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(629669, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100653', 'abnormal myoblast', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(629670, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0142051', 'abnormal cerebrospinal fluid', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(629671, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0127557', 'abnormally localised hepato-pancreatic duct', 0.40540540540540543, 5.05060299610679, 1.4309233924911664, 'HP:0025031', 'Abnormality of the digestive system'),
(629672, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100274', 'abnormal sensory system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(629673, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100003', 'abnormal organism subdivision', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(629674, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0101513', 'abnormal basal body', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(629675, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0126061', 'absent manicotto glandulare', 0.42857142857142855, 5.05060299610679, 1.471238981671103, 'HP:0025031', 'Abnormality of the digestive system'),
(629676, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100277', 'abnormal blastocoel', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(629677, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0101497', 'abnormal ciliary axoneme', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(629678, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0107289', 'abnormal cloacal sphincter', 0.4166666666666667, 5.05060299610679, 1.45066119926208, 'HP:0025031', 'Abnormality of the digestive system'),
(629679, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0101405', 'abnormal ring structure', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(629680, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100665', 'abnormal egg jelly', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(629681, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100377', 'abnormal connective tissue', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(629682, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0127838', 'abnormally localised dorsal foregut', 0.4411764705882353, 5.05060299610679, 1.4927180591674907, 'HP:0025031', 'Abnormality of the digestive system'),
(629683, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100742', 'abnormal musculoskeletal system', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(629684, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0101240', 'abnormal ciliated non-epidermal cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(629685, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0124888', 'absent liver and biliary system', 0.45454545454545453, 5.05060299610679, 1.5151662069205463, 'HP:0025031', 'Abnormality of the digestive system'),
(629686, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0101569', 'abnormal activin-induced ectoderm', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(629687, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100571', 'abnormal branchial arch 1', 0.46875, 5.05060299610679, 1.5386585568036393, 'HP:0025031', 'Abnormality of the digestive system'),
(629688, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100204', 'abnormal islets of Langerhans', 0.42105263157894735, 7.1173123385767045, 1.731116139930257, 'HP:0002012', 'Abnormality of the abdominal organs'),
(629689, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100640', 'abnormal notochordal sheath', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(629690, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0101109', 'abnormal egg cell-free extract', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(629691, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0101467', 'abnormal alkali secreting cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(629692, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100989', 'abnormal right blastomere', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(629693, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0127881', 'abnormally localised digestive enzyme secreting cell', 0.4166666666666667, 5.05060299610679, 1.45066119926208, 'HP:0025031', 'Abnormality of the digestive system'),
(629694, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100894', 'abnormal nucleus', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(629695, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0101468', 'abnormal stage I oocyte', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(629696, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0131437', 'abnormally decreased number of cilium in the alimentary system', 0.4166666666666667, 5.05060299610679, 1.45066119926208, 'HP:0025031', 'Abnormality of the digestive system'),
(629697, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0101071', 'abnormal endoplasmic reticulum', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(629698, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100372', 'abnormal hematological system', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(629699, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100572', 'abnormal branchial arch', 0.4838709677419355, 5.05060299610679, 1.5632786569919361, 'HP:0025031', 'Abnormality of the digestive system'),
(629700, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100010', 'abnormal multicellular anatomical structure', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(629701, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100643', 'abnormal thoracic region', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(629702, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100084', 'abnormal anatomical group', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(629703, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0141791', 'abnormal primary metabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(629704, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100802', 'abnormal exocrine cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(629705, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100610', 'abnormal appendage', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(629706, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100344', 'abnormal portion of organism substance', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(629707, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0102094', 'abnormal anterior foregut morphology', 0.40540540540540543, 5.05060299610679, 1.4309233924911664, 'HP:0025031', 'Abnormality of the digestive system'),
(629708, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0131675', 'abnormal spindle microtubule', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(629709, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0125663', 'absent oral evagination', 0.4411764705882353, 5.05060299610679, 1.4927180591674907, 'HP:0025031', 'Abnormality of the digestive system'),
(629710, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100402', 'abnormal zeugopod', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(629711, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100339', 'abnormal circumblastoporal collar', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(629712, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0115512', 'abnormally semi-erect whole organism', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(629713, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0101503', 'abnormal organ cortex', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(629714, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100415', 'abnormal secretory epithelial cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(629715, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100481', 'abnormal anatomical line', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(629716, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100969', 'abnormal disaggregated/reaggregated ectoderm treated with activin', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(629717, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0141841', 'abnormality of whole organism mass', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(629718, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0141265', 'abnormal escape behavior', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(629719, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100531', 'abnormal proliferative region', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(629720, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0101406', 'abnormal cleavage furrow', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(629721, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100841', 'abnormal large intestine', 0.40540540540540543, 5.05060299610679, 1.4309233924911664, 'HP:0025031', 'Abnormality of the digestive system'),
(629722, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100976', 'abnormal multiciliated cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(629723, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0128341', 'decreased size of the pharyngeal cavity', 0.40540540540540543, 5.05060299610679, 1.4309233924911664, 'HP:0025031', 'Abnormality of the digestive system'),
(629724, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0141777', 'abnormal catabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(629725, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100060', 'abnormal regenerating tissue', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(629726, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0107375', 'abnormal larval alimentary system morphology', 0.4411764705882353, 5.05060299610679, 1.4927180591674907, 'HP:0025031', 'Abnormality of the digestive system'),
(629727, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0141315', 'abnormal anatomical region', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(629728, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100986', 'abnormal gut epithelium', 0.5769230769230769, 5.05060299610679, 1.706988406765213, 'HP:0025031', 'Abnormality of the digestive system'),
(629729, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0131723', 'abnormal pathway-restricted SMAD protein phosphorylation', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(629730, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100176', 'abnormal stage VI oocyte', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(629731, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0107269', 'abnormal right side', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(629732, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0107273', 'abnormal basal region', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(629733, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100218', 'abnormal epithelial cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(629734, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0141267', 'abnormal resting posture', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(629735, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100202', 'abnormal embryo', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(629736, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0141776', 'abnormal metabolic process', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(629737, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0141796', 'abnormal demethylation', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(629738, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0126466', 'abnormally localised alimentary system', 0.4838709677419355, 5.05060299610679, 1.5632786569919361, 'HP:0025031', 'Abnormality of the digestive system'),
(629739, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0101084', 'abnormal mesentery', 0.4838709677419355, 5.05060299610679, 1.5632786569919361, 'HP:0025031', 'Abnormality of the digestive system'),
(629740, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0101463', 'abnormal right-ventral blastomere', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(629741, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100225', 'abnormal endocrine system', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(629742, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0115508', 'abnormally peramorphic growth of whole organism', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(629743, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0141718', 'abnormal posterior notochord', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(629744, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100862', 'abnormal blastomere V1', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(629745, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0107288', 'abnormal larval alimentary system', 0.6521739130434783, 5.05060299610679, 1.814902619756796, 'HP:0025031', 'Abnormality of the digestive system'),
(629746, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0141717', 'abnormal tracheoesophageal fold', 0.5172413793103449, 5.05060299610679, 1.6162861318637973, 'HP:0025031', 'Abnormality of the digestive system'),
(629747, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100004', 'abnormal cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(629748, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0102522', 'abnormal pharyngeal cavity morphology', 0.46875, 5.05060299610679, 1.5386585568036393, 'HP:0025031', 'Abnormality of the digestive system'),
(629749, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0101547', 'abnormal lampbrush chromosome', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(629750, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100214', 'abnormal second pancreatic bud', 0.5172413793103449, 5.05060299610679, 1.6162861318637973, 'HP:0025031', 'Abnormality of the digestive system'),
(629751, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0129821', 'increased size of the pharyngeal cavity', 0.40540540540540543, 5.05060299610679, 1.4309233924911664, 'HP:0025031', 'Abnormality of the digestive system'),
(629752, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0101435', 'abnormal paracrine cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(629753, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100458', 'abnormal autopod', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(629754, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0141784', 'abnormal cellular hormone metabolic process', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(629755, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0101448', 'abnormal myelin accumulating cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(629756, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100028', 'abnormal anatomical cluster', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(629757, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100907', 'abnormal cytoplasm', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(629758, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0101373', 'abnormal oxygen accumulating cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(629759, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0131687', 'abnormal astral microtubule', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(629760, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0124991', 'absent foregut', 0.42857142857142855, 5.05060299610679, 1.471238981671103, 'HP:0025031', 'Abnormality of the digestive system'),
(629761, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0101237', 'abnormal mucus secreting cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(629762, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100533', 'abnormal melanoblast', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(629763, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100724', 'abnormal kinetochore', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(629764, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100002', 'abnormal head', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(629765, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100591', 'abnormal pharyngeal arch', 0.5, 5.05060299610679, 1.5891197242666757, 'HP:0025031', 'Abnormality of the digestive system'),
(629766, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100156', 'abnormal foregut', 0.6, 5.05060299610679, 1.740793439114496, 'HP:0025031', 'Abnormality of the digestive system'),
(629767, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100587', 'abnormal vestibuloauditory system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(629768, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0101169', 'abnormal hepato-pancreatic duct', 0.5555555555555556, 5.05060299610679, 1.6750792677938144, 'HP:0025031', 'Abnormality of the digestive system'),
(629769, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100285', 'abnormal progenitor cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(629770, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0107272', 'abnormal axial region', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(629771, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0101132', 'abnormal apoptotic cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(629772, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0131725', 'abnormal phosphorylation of RNA polymerase II C-terminal domain', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(629773, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0126972', 'abnormally localised gut epithelium', 0.40540540540540543, 5.05060299610679, 1.4309233924911664, 'HP:0025031', 'Abnormality of the digestive system'),
(629774, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0141770', 'abnormal urate homeostasis', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(629775, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100912', 'abnormal trabecula', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(629776, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0125214', 'absent midgut', 0.42857142857142855, 5.05060299610679, 1.471238981671103, 'HP:0025031', 'Abnormality of the digestive system'),
(629777, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100493', 'abnormal liver and biliary system', 0.6521739130434783, 5.05060299610679, 1.814902619756796, 'HP:0025031', 'Abnormality of the digestive system'),
(629778, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0131677', 'abnormal actin filament', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(629779, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0141272', 'absent surface breathing', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(629780, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0107253', 'abnormal enteric nervous system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(629781, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100231', 'abnormal compound organ', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(629782, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0127721', 'abnormally localised manicotto glandulare', 0.4411764705882353, 5.05060299610679, 1.4927180591674907, 'HP:0025031', 'Abnormality of the digestive system'),
(629783, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100523', 'abnormal midgut', 0.6, 5.05060299610679, 1.740793439114496, 'HP:0025031', 'Abnormality of the digestive system'),
(629784, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100581', 'abnormal immune system', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(629785, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100386', 'abnormal limb', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(629786, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100317', 'abnormal respiratory system', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(629787, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0131662', 'abnormal foregut epithelium', 0.5, 5.05060299610679, 1.5891197242666757, 'HP:0025031', 'Abnormality of the digestive system'),
(629788, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0101283', 'abnormal left-ventral blastomere', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(629789, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0101356', 'abnormal exocrine pancreas', 0.45714285714285713, 7.1173123385767045, 1.8037817211722333, 'HP:0002012', 'Abnormality of the abdominal organs'),
(629790, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0141743', 'abnormal chemical homeostasis within a tissue', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(629791, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0127678', 'abnormally localised ventral foregut', 0.4411764705882353, 5.05060299610679, 1.4927180591674907, 'HP:0025031', 'Abnormality of the digestive system'),
(629792, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0101228', 'abnormal mesenchymal stem cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(629793, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100674', 'abnormal secondary oogonium', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(629794, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100574', 'abnormal gastrula cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(629795, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100585', 'abnormal elastica externa', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(629796, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0101074', 'abnormal germinal vesicle', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(629797, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100465', 'abnormal skeletal system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(629798, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0131666', 'abnormal adherens junction', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(629799, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0126705', 'abnormally localised larval alimentary system', 0.45454545454545453, 5.05060299610679, 1.5151662069205463, 'HP:0025031', 'Abnormality of the digestive system'),
(629800, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0101377', 'abnormal manicotto glandulare', 0.6, 5.05060299610679, 1.740793439114496, 'HP:0025031', 'Abnormality of the digestive system'),
(629801, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100762', 'abnormal intersomitic region', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(629802, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0126019', 'absent ventral foregut', 0.42857142857142855, 5.05060299610679, 1.471238981671103, 'HP:0025031', 'Abnormality of the digestive system'),
(629803, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100866', 'abnormal liver primordium', 0.4411764705882353, 5.05060299610679, 1.4927180591674907, 'HP:0025031', 'Abnormality of the digestive system'),
(629804, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100715', 'abnormal ciliated cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(629805, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100477', 'abnormal pericyte', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(629806, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0115392', 'abnormally incomplete structure of alimentary system', 0.45454545454545453, 5.05060299610679, 1.5151662069205463, 'HP:0025031', 'Abnormality of the digestive system'),
(629807, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0141821', 'metaplastic esophagus', 0.42857142857142855, 5.05060299610679, 1.471238981671103, 'HP:0025031', 'Abnormality of the digestive system'),
(629808, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0141794', 'abnormal prosthetic group metabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(629809, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0102733', 'abnormal posterior foregut morphology', 0.40540540540540543, 5.05060299610679, 1.4309233924911664, 'HP:0025031', 'Abnormality of the digestive system'),
(629810, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0101297', 'abnormal barrier cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(629811, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100416', 'abnormal ligament', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(629812, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100791', 'abnormal multiciliated cell precursor', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(629813, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0141264', 'abnormal schooling behavior', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(629814, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100114', 'abnormal peripheral nervous system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(629815, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0107268', 'abnormal left side', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(629816, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100667', 'abnormal vegetal yolk mass', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(629817, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100437', 'abnormal proepicardium', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(629818, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0142056', 'abnormal main body axis', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(629819, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0102367', 'abnormal hindgut morphology', 0.4166666666666667, 5.05060299610679, 1.45066119926208, 'HP:0025031', 'Abnormality of the digestive system'),
(629820, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100031', 'abnormal central nervous system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(629821, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100268', 'abnormal circulatory system', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(629822, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100104', 'abnormal embryonic structure', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(629823, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0141499', 'abnormal tadpole', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(629824, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100392', 'abnormal cilium', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(629825, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0107263', 'abnormal anatomical side', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(629826, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100384', 'abnormal amputated tissue', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(629827, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100856', 'abnormal simple organ', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(629828, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0142027', 'abnormally localised digestive tract', 0.45454545454545453, 5.05060299610679, 1.5151662069205463, 'HP:0025031', 'Abnormality of the digestive system'),
(629829, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100691', 'abnormal keratin accumulating cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(629830, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100192', 'abnormal epithelium', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(629831, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0101347', 'abnormal hindlimb region', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(629832, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100893', 'abnormal hyoid arch', 0.4838709677419355, 5.05060299610679, 1.5632786569919361, 'HP:0025031', 'Abnormality of the digestive system'),
(629833, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0101220', 'abnormal centriole', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(629834, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100108', 'abnormal cell part', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(629835, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0127307', 'abnormally localised oral evagination', 0.45454545454545453, 5.05060299610679, 1.5151662069205463, 'HP:0025031', 'Abnormality of the digestive system'),
(629836, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0131669', 'abnormal Roux spot', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(629837, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0126813', 'abnormally localised gall bladder primordium', 0.40540540540540543, 5.05060299610679, 1.4309233924911664, 'HP:0025031', 'Abnormality of the digestive system'),
(629838, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0101004', 'abnormal acid secreting cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(629839, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100662', 'abnormal lung primordium', 0.45454545454545453, 5.05060299610679, 1.5151662069205463, 'HP:0025031', 'Abnormality of the digestive system'),
(629840, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100308', 'abnormal early embryonic cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(629841, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0107312', 'abnormal filopodium', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(629842, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0107278', 'abnormal medial region', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(629843, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100902', 'abnormal spermatocyte', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(629844, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100186', 'abnormal uveal tract', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(629845, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0101601', 'abnormal proctodeum', 0.5555555555555556, 5.05060299610679, 1.6750792677938144, 'HP:0025031', 'Abnormality of the digestive system'),
(629846, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0141782', 'abnormal methylation', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(629847, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0107267', 'abnormal ventral side', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(629848, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0107262', 'abnormal left-right axis', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(629849, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100483', 'abnormal cloaca', 0.42857142857142855, 5.05060299610679, 1.471238981671103, 'HP:0025031', 'Abnormality of the digestive system'),
(629850, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100735', 'abnormal hindgut', 0.6, 5.05060299610679, 1.740793439114496, 'HP:0025031', 'Abnormality of the digestive system'),
(629851, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0141783', 'abnormal collagen metabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(629852, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0107308', 'abnormal anterior hindgut endoderm', 0.5172413793103449, 5.05060299610679, 1.6162861318637973, 'HP:0025031', 'Abnormality of the digestive system'),
(629853, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0107258', 'abnormal anatomical axis', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(629854, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100813', 'abnormal branchial arch 3', 0.46875, 5.05060299610679, 1.5386585568036393, 'HP:0025031', 'Abnormality of the digestive system'),
(629855, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100718', 'abnormal ventral pancreatic bud', 0.5555555555555556, 5.05060299610679, 1.6750792677938144, 'HP:0025031', 'Abnormality of the digestive system'),
(629856, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100307', 'abnormal blastomere', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(629857, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100956', 'abnormal centrosome', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(629858, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0101411', 'abnormal marginal zone (sensu neural)', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(629859, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0101101', 'abnormal posterior foregut', 0.5769230769230769, 5.05060299610679, 1.706988406765213, 'HP:0025031', 'Abnormality of the digestive system'),
(629860, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100032', 'abnormal nervous system', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(629861, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0142057', 'abnormal desmosome', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(629862, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100025', 'abnormal oocyte', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(629863, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0103009', 'abnormal manicotto glandulare morphology', 0.42857142857142855, 5.05060299610679, 1.471238981671103, 'HP:0025031', 'Abnormality of the digestive system'),
(629864, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0101136', 'abnormal ooplasm', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(629865, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0101302', 'abnormal subcortical cytoplasm', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(629866, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0126425', 'abnormally localised posterior foregut', 0.4411764705882353, 5.05060299610679, 1.4927180591674907, 'HP:0025031', 'Abnormality of the digestive system'),
(629867, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100900', 'abnormal angioblast', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(629868, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0100337', 'abnormal zygote', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(629869, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0101788', 'abnormal foregut morphology', 0.4166666666666667, 5.05060299610679, 1.45066119926208, 'HP:0025031', 'Abnormality of the digestive system'),
(629870, 'HP:0002012', 'Abnormality of the abdominal organs', 'XPO:0141715', 'abnormal septum', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(629871, 'HP:0100387', 'Aplasia of the middle phalanges of the toes', 'XPO:0102876', 'abnormal hindlimb digit 4 morphology', 0.4095238095238095, 7.639349617137506, 1.7687553696015759, 'UPHENO:0088132', 'abnormal pedal digit morphology'),
(629872, 'HP:0100387', 'Aplasia of the middle phalanges of the toes', 'XPO:0139979', 'abnormally necrotic claw primordium', 0.40186915887850466, 7.639349617137506, 1.752146970153439, 'UPHENO:0088132', 'abnormal pedal digit morphology'),
(629873, 'HP:0100387', 'Aplasia of the middle phalanges of the toes', 'XPO:0102948', 'abnormal hindlimb digit 5 morphology', 0.4095238095238095, 7.639349617137506, 1.7687553696015759, 'HP:0001780', 'Abnormal toe morphology'),
(629874, 'HP:0100387', 'Aplasia of the middle phalanges of the toes', 'XPO:0101872', 'abnormal hindlimb digit 1 morphology', 0.4095238095238095, 7.639349617137506, 1.7687553696015759, 'UPHENO:0088132', 'abnormal pedal digit morphology'),
(629875, 'HP:0100387', 'Aplasia of the middle phalanges of the toes', 'XPO:0103571', 'decreased length of hindlimb digit', 0.42276422764227645, 10.299160507394836, 2.086652016334447, 'HP:0006494', 'Aplasia/Hypoplasia involving bones of the feet'),
(629876, 'HP:0100387', 'Aplasia of the middle phalanges of the toes', 'XPO:0102566', 'abnormal claw primordium morphology', 0.4215686274509804, 7.639349617137506, 1.7945779817870358, 'UPHENO:0088132', 'abnormal pedal digit morphology'),
(629877, 'HP:0100387', 'Aplasia of the middle phalanges of the toes', 'XPO:0103289', 'absent hindlimb digit', 0.4017094017094017, 10.299160507394836, 2.034027926439231, 'HP:0006494', 'Aplasia/Hypoplasia involving bones of the feet'),
(629878, 'HP:0100387', 'Aplasia of the middle phalanges of the toes', 'XPO:0102051', 'abnormal hindlimb digit 2 morphology', 0.4095238095238095, 7.639349617137506, 1.7687553696015759, 'HP:0001780', 'Abnormal toe morphology'),
(629879, 'HP:0100387', 'Aplasia of the middle phalanges of the toes', 'XPO:0101809', 'abnormal hindlimb digit morphology', 0.4174757281553398, 7.639349617137506, 1.7858451903924082, 'HP:0001780', 'Abnormal toe morphology'),
(629880, 'HP:0100387', 'Aplasia of the middle phalanges of the toes', 'XPO:0102180', 'abnormal hindlimb digit 3 morphology', 0.4095238095238095, 7.639349617137506, 1.7687553696015759, 'HP:0001780', 'Abnormal toe morphology'),
(629881, 'HP:0100387', 'Aplasia of the middle phalanges of the toes', 'XPO:0141512', 'decreased length of hindlimb digit in regenerating tissue', 0.4126984126984127, 10.299160507394836, 2.0616612703177086, 'HP:0006494', 'Aplasia/Hypoplasia involving bones of the feet'),
(629882, 'HP:0005021', 'Bilateral elbow dislocations', 'XPO:0103218', 'abnormal joint morphology', 0.40350877192982454, 9.103525386846629, 1.9165991623389758, 'UPHENO:0016527', 'abnormal skeletal joint morphology in the independent continuant'),
(629883, 'HP:0005021', 'Bilateral elbow dislocations', 'XPO:0100970', 'abnormal carpus', 0.4246575342465753, 9.696350005340756, 2.02919394944391, 'HP:0009810', 'Abnormality of upper limb joint'),
(629884, 'HP:0031382', 'Decreased lymphocyte proliferation in response to anti-CD3', 'XPO:0131706', 'abnormal ciliary basal body organization', 0.4634146341463415, 6.160501005184397, 1.6896349663390897, 'UPHENO:0049858', 'abnormal cell population proliferation'),
(629885, 'HP:0031382', 'Decreased lymphocyte proliferation in response to anti-CD3', 'XPO:0131708', 'abnormal cilium disassembly', 0.4634146341463415, 6.160501005184397, 1.6896349663390897, 'UPHENO:0049858', 'abnormal cell population proliferation'),
(629886, 'HP:0031382', 'Decreased lymphocyte proliferation in response to anti-CD3', 'XPO:0131707', 'abnormal cilium assembly', 0.4418604651162791, 6.160501005184397, 1.6498732798309337, 'UPHENO:0049858', 'abnormal cell population proliferation'),
(629887, 'HP:0031382', 'Decreased lymphocyte proliferation in response to anti-CD3', 'XPO:0103642', 'increased cell population proliferation', 0.4418604651162791, 6.160501005184397, 1.6498732798309337, 'UPHENO:0049858', 'abnormal cell population proliferation'),
(629888, 'HP:0001773', 'Short foot', 'XPO:0102180', 'abnormal hindlimb digit 3 morphology', 0.41304347826086957, 7.61213700143767, 1.7731732978116046, 'UPHENO:0079871', 'abnormal anatomical entity morphology in the skeleton of pelvic complex'),
(629889, 'HP:0001773', 'Short foot', 'XPO:0115990', 'abnormally decreased length of hindlimb digit 3 in regenerating tissue', 0.4774774774774775, 10.299160507394836, 2.217570106942855, 'HP:0006494', 'Aplasia/Hypoplasia involving bones of the feet'),
(629890, 'HP:0001773', 'Short foot', 'XPO:0102880', 'abnormal digit-joint region morphology', 0.41333333333333333, 6.173473740856008, 1.5974049203485685, 'UPHENO:0087006', 'abnormal autopod region morphology'),
(629891, 'HP:0001773', 'Short foot', 'XPO:0102876', 'abnormal hindlimb digit 4 morphology', 0.41304347826086957, 7.61213700143767, 1.7731732978116046, 'UPHENO:0079871', 'abnormal anatomical entity morphology in the skeleton of pelvic complex'),
(629892, 'HP:0001773', 'Short foot', 'XPO:0103817', 'decreased length of hindlimb digit 2 in regenerating hindlimb', 0.452991452991453, 10.299160507394836, 2.1599610373423355, 'HP:0006494', 'Aplasia/Hypoplasia involving bones of the feet'),
(629893, 'HP:0001773', 'Short foot', 'XPO:0101810', 'abnormal digit morphology', 0.41333333333333333, 6.173473740856008, 1.5974049203485685, 'UPHENO:0087006', 'abnormal autopod region morphology'),
(629894, 'HP:0001773', 'Short foot', 'XPO:0115992', 'abnormally decreased length of hindlimb digit 5 in regenerating tissue', 0.4774774774774775, 10.299160507394836, 2.217570106942855, 'HP:0006494', 'Aplasia/Hypoplasia involving bones of the feet'),
(629895, 'HP:0001773', 'Short foot', 'XPO:0141512', 'decreased length of hindlimb digit in regenerating tissue', 0.4953271028037383, 10.299160507394836, 2.2586397090812342, 'HP:0006494', 'Aplasia/Hypoplasia involving bones of the feet'),
(629896, 'HP:0001773', 'Short foot', 'XPO:0128670', 'decreased size of the claw primordium', 0.44086021505376344, 7.61213700143767, 1.8319083916704244, 'UPHENO:0079871', 'abnormal anatomical entity morphology in the skeleton of pelvic complex'),
(629897, 'HP:0001773', 'Short foot', 'XPO:0128213', 'decreased size of the digit', 0.41975308641975306, 6.173473740856008, 1.609762298184303, 'UPHENO:0087006', 'abnormal autopod region morphology'),
(629898, 'HP:0001773', 'Short foot', 'XPO:0139979', 'abnormally necrotic claw primordium', 0.40425531914893614, 7.61213700143767, 1.7542083322460909, 'UPHENO:0079871', 'abnormal anatomical entity morphology in the skeleton of pelvic complex'),
(629899, 'HP:0001773', 'Short foot', 'XPO:0103816', 'decreased length of hindlimb digit 1 in regenerating hindlimb', 0.452991452991453, 10.299160507394836, 2.1599610373423355, 'HP:0006494', 'Aplasia/Hypoplasia involving bones of the feet'),
(629900, 'HP:0001773', 'Short foot', 'XPO:0115988', 'abnormally decreased length of hindlimb digit 1 in regenerating tissue', 0.4774774774774775, 10.299160507394836, 2.217570106942855, 'HP:0006494', 'Aplasia/Hypoplasia involving bones of the feet'),
(629901, 'HP:0001773', 'Short foot', 'XPO:0102948', 'abnormal hindlimb digit 5 morphology', 0.41304347826086957, 7.61213700143767, 1.7731732978116046, 'UPHENO:0079871', 'abnormal anatomical entity morphology in the skeleton of pelvic complex'),
(629902, 'HP:0001773', 'Short foot', 'XPO:0101809', 'abnormal hindlimb digit morphology', 0.4222222222222222, 7.61213700143767, 1.7927669677364697, 'UPHENO:0079871', 'abnormal anatomical entity morphology in the skeleton of pelvic complex'),
(629903, 'HP:0001773', 'Short foot', 'XPO:0115989', 'abnormally decreased length of hindlimb digit 2 in regenerating tissue', 0.4774774774774775, 10.299160507394836, 2.217570106942855, 'HP:0006494', 'Aplasia/Hypoplasia involving bones of the feet'),
(629904, 'HP:0001773', 'Short foot', 'XPO:0129321', 'decreased size of the hindlimb digit 4', 0.41, 7.61213700143767, 1.7666284755401869, 'UPHENO:0079871', 'abnormal anatomical entity morphology in the skeleton of pelvic complex'),
(629905, 'HP:0001773', 'Short foot', 'XPO:0128497', 'decreased size of the digit-joint region', 0.4358974358974359, 6.173473740856008, 1.6404271925993197, 'UPHENO:0087006', 'abnormal autopod region morphology'),
(629906, 'HP:0001773', 'Short foot', 'XPO:0128451', 'decreased size of the hindlimb digit 5', 0.41, 7.61213700143767, 1.7666284755401869, 'UPHENO:0079871', 'abnormal anatomical entity morphology in the skeleton of pelvic complex'),
(629907, 'HP:0001773', 'Short foot', 'XPO:0102566', 'abnormal claw primordium morphology', 0.42696629213483145, 7.61213700143767, 1.8028105587460364, 'UPHENO:0079871', 'abnormal anatomical entity morphology in the skeleton of pelvic complex'),
(629908, 'HP:0001773', 'Short foot', 'XPO:0128802', 'decreased size of the hindlimb digit 3', 0.41, 7.61213700143767, 1.7666284755401869, 'UPHENO:0079871', 'abnormal anatomical entity morphology in the skeleton of pelvic complex'),
(629909, 'HP:0001773', 'Short foot', 'XPO:0103571', 'decreased length of hindlimb digit', 0.5096153846153846, 10.299160507394836, 2.2909846449052425, 'HP:0006494', 'Aplasia/Hypoplasia involving bones of the feet'),
(629910, 'HP:0001773', 'Short foot', 'XPO:0128272', 'decreased size of the hindlimb digit 2', 0.41, 7.61213700143767, 1.7666284755401869, 'UPHENO:0079871', 'abnormal anatomical entity morphology in the skeleton of pelvic complex'),
(629911, 'HP:0001773', 'Short foot', 'XPO:0103819', 'decreased length of hindlimb digit 4 in regenerating hindlimb', 0.452991452991453, 10.299160507394836, 2.1599610373423355, 'HP:0006494', 'Aplasia/Hypoplasia involving bones of the feet'),
(629912, 'HP:0001773', 'Short foot', 'XPO:0128168', 'decreased size of the hindlimb digit 1', 0.41, 7.61213700143767, 1.7666284755401869, 'UPHENO:0079871', 'abnormal anatomical entity morphology in the skeleton of pelvic complex'),
(629913, 'HP:0001773', 'Short foot', 'XPO:0103818', 'decreased length of hindlimb digit 3 in regenerating hindlimb', 0.452991452991453, 10.299160507394836, 2.1599610373423355, 'HP:0006494', 'Aplasia/Hypoplasia involving bones of the feet'),
(629914, 'HP:0001773', 'Short foot', 'XPO:0103289', 'absent hindlimb digit', 0.40384615384615385, 10.299160507394836, 2.0394304005666894, 'HP:0006494', 'Aplasia/Hypoplasia involving bones of the feet'),
(629915, 'HP:0001773', 'Short foot', 'XPO:0103436', 'decreased size of the hindlimb digit', 0.422680412371134, 7.61213700143767, 1.7937394478555804, 'UPHENO:0079871', 'abnormal anatomical entity morphology in the skeleton of pelvic complex'),
(629916, 'HP:0001773', 'Short foot', 'XPO:0129382', 'decreased size of the iliac process', 0.41935483870967744, 7.61213700143767, 1.7866691032404018, 'UPHENO:0079871', 'abnormal anatomical entity morphology in the skeleton of pelvic complex'),
(629917, 'HP:0001773', 'Short foot', 'XPO:0115991', 'abnormally decreased length of hindlimb digit 4 in regenerating tissue', 0.4774774774774775, 10.299160507394836, 2.217570106942855, 'HP:0006494', 'Aplasia/Hypoplasia involving bones of the feet'),
(629918, 'HP:0001773', 'Short foot', 'XPO:0130149', 'increased size of the claw primordium', 0.4105263157894737, 7.61213700143767, 1.7677620197540558, 'UPHENO:0079871', 'abnormal anatomical entity morphology in the skeleton of pelvic complex'),
(629919, 'HP:0001773', 'Short foot', 'XPO:0102051', 'abnormal hindlimb digit 2 morphology', 0.41304347826086957, 7.61213700143767, 1.7731732978116046, 'UPHENO:0079871', 'abnormal anatomical entity morphology in the skeleton of pelvic complex'),
(629920, 'HP:0001773', 'Short foot', 'XPO:0101872', 'abnormal hindlimb digit 1 morphology', 0.41304347826086957, 7.61213700143767, 1.7731732978116046, 'UPHENO:0079871', 'abnormal anatomical entity morphology in the skeleton of pelvic complex'),
(629921, 'HP:0001773', 'Short foot', 'XPO:0103820', 'decreased length of hindlimb digit 5 in regenerating hindlimb', 0.452991452991453, 10.299160507394836, 2.1599610373423355, 'HP:0006494', 'Aplasia/Hypoplasia involving bones of the feet'),
(629922, 'HP:0006713', 'Aplasia/Hypoplasia of the scapulae', 'XPO:0102400', 'abnormal pectoral girdle morphology', 0.48148148148148145, 10.335532897059798, 2.2307773737369985, 'UPHENO:0002982', 'abnormal pectoral girdle region'),
(629923, 'HP:0006713', 'Aplasia/Hypoplasia of the scapulae', 'XPO:0102865', 'abnormal scapula morphology', 0.42990654205607476, 10.335532897059798, 2.107916793443655, 'UPHENO:0002982', 'abnormal pectoral girdle region'),
(629924, 'HP:0006713', 'Aplasia/Hypoplasia of the scapulae', 'XPO:0130099', 'increased size of the pectoral girdle', 0.43820224719101125, 10.335532897059798, 2.128157358234636, 'UPHENO:0002982', 'abnormal pectoral girdle region'),
(629925, 'HP:0006713', 'Aplasia/Hypoplasia of the scapulae', 'XPO:0102383', 'abnormal coracoid bone morphology', 0.42990654205607476, 10.335532897059798, 2.107916793443655, 'UPHENO:0002982', 'abnormal pectoral girdle region'),
(629926, 'HP:0006713', 'Aplasia/Hypoplasia of the scapulae', 'XPO:0128619', 'decreased size of the pectoral girdle', 0.43333333333333335, 10.335532897059798, 2.116301236133279, 'UPHENO:0002982', 'abnormal pectoral girdle region'),
(629927, 'HP:0006713', 'Aplasia/Hypoplasia of the scapulae', 'XPO:0140731', 'abnormally necrotic pectoral girdle', 0.4482758620689655, 10.335532897059798, 2.152479946334375, 'UPHENO:0002982', 'abnormal pectoral girdle region'),
(629928, 'HP:0011826', 'Philtrum with midline raphe', 'XPO:0115393', 'abnormally decreased volume of oral cavity', 0.4861111111111111, 7.884497199543557, 1.9577389239177327, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(629929, 'HP:0011826', 'Philtrum with midline raphe', 'XPO:0140897', 'abnormally necrotic lower jaw', 0.40476190476190477, 7.312692920701687, 1.7204358504524693, 'UPHENO:0076800', 'abnormal mouth morphology'),
(629930, 'HP:0011826', 'Philtrum with midline raphe', 'XPO:0141830', 'increased width of mouth', 0.4430379746835443, 7.884497199543557, 1.8689921537245293, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(629931, 'HP:0011826', 'Philtrum with midline raphe', 'XPO:0103138', 'abnormal upper jaw morphology', 0.45569620253164556, 8.81758714901448, 2.00453011434045, 'UPHENO:0087585', 'abnormal midface morphology'),
(629932, 'HP:0011826', 'Philtrum with midline raphe', 'XPO:0103199', 'abnormal tongue morphology', 0.5384615384615384, 7.884497199543557, 2.060460747517874, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(629933, 'HP:0011826', 'Philtrum with midline raphe', 'XPO:0126089', 'absent tongue', 0.4647887323943662, 7.884497199543557, 1.9143211483298146, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(629934, 'HP:0011826', 'Philtrum with midline raphe', 'XPO:0101659', 'abnormal lower jaw morphology', 0.43037974683544306, 7.312692920701687, 1.7740447930920258, 'UPHENO:0076800', 'abnormal mouth morphology'),
(629935, 'HP:0011826', 'Philtrum with midline raphe', 'XPO:0130701', 'increased size of the upper jaw', 0.4186046511627907, 8.81758714901448, 1.9212191422663665, 'UPHENO:0087585', 'abnormal midface morphology'),
(629936, 'HP:0011826', 'Philtrum with midline raphe', 'XPO:0102279', 'abnormal mouth morphology', 0.5076923076923077, 7.312692920701687, 1.9268103031581083, 'UPHENO:0076800', 'abnormal mouth morphology'),
(629937, 'HP:0011826', 'Philtrum with midline raphe', 'XPO:0101816', 'abnormal tooth morphology', 0.4166666666666667, 7.884497199543557, 1.812514045870123, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(629938, 'HP:0011826', 'Philtrum with midline raphe', 'XPO:0102960', 'abnormal oral epithelium morphology', 0.44594594594594594, 7.312692920701687, 1.8058421198805104, 'UPHENO:0076800', 'abnormal mouth morphology'),
(629939, 'HP:0011826', 'Philtrum with midline raphe', 'XPO:0103096', 'abnormal oral cavity morphology', 0.5384615384615384, 7.884497199543557, 2.060460747517874, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(629940, 'HP:0011826', 'Philtrum with midline raphe', 'XPO:0101483', 'abnormal nostril', 0.4126984126984127, 9.116652820832241, 1.9396979528472913, 'HP:0000366', 'Abnormality of the nose'),
(629941, 'HP:0011826', 'Philtrum with midline raphe', 'XPO:0102223', 'abnormal pharyngeal arch morphology', 0.4153846153846154, 5.725717590856133, 1.5421981063659433, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(629942, 'HP:0011826', 'Philtrum with midline raphe', 'XPO:0127750', 'abnormally localised tongue', 0.4782608695652174, 7.884497199543557, 1.9418667530853457, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(629943, 'HP:0011826', 'Philtrum with midline raphe', 'XPO:0140639', 'abnormally necrotic upper jaw', 0.42857142857142855, 8.81758714901448, 1.9439562549106413, 'UPHENO:0087585', 'abnormal midface morphology'),
(629944, 'HP:0011826', 'Philtrum with midline raphe', 'XPO:0102204', 'abnormal branchial arch morphology', 0.40298507462686567, 5.725717590856133, 1.5190058362769763, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(629945, 'HP:0011826', 'Philtrum with midline raphe', 'XPO:0131611', 'increased size of the roof of mouth', 0.44, 7.312692920701687, 1.7937627728071353, 'UPHENO:0076800', 'abnormal mouth morphology'),
(629946, 'HP:0011826', 'Philtrum with midline raphe', 'XPO:0141311', 'abnormal roof of mouth morphology', 0.4852941176470588, 7.312692920701687, 1.8838277146745184, 'UPHENO:0076800', 'abnormal mouth morphology'),
(629947, 'HP:0011826', 'Philtrum with midline raphe', 'XPO:0131573', 'decreased size of the roof of mouth', 0.44, 7.312692920701687, 1.7937627728071353, 'UPHENO:0076800', 'abnormal mouth morphology'),
(629948, 'HP:0011826', 'Philtrum with midline raphe', 'XPO:0140789', 'abnormally necrotic roof of mouth', 0.4520547945205479, 7.312692920701687, 1.8181688303509294, 'UPHENO:0076800', 'abnormal mouth morphology'),
(629949, 'HP:0011826', 'Philtrum with midline raphe', 'XPO:0140626', 'abnormally necrotic tongue', 0.5, 7.884497199543557, 1.9855096574360394, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(629950, 'HP:0011826', 'Philtrum with midline raphe', 'XPO:0129152', 'decreased size of the oral cavity', 0.5, 7.884497199543557, 1.9855096574360394, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(629951, 'HP:0011826', 'Philtrum with midline raphe', 'XPO:0128105', 'decreased size of the tongue', 0.44871794871794873, 7.884497199543557, 1.880934717115827, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(629952, 'HP:0011826', 'Philtrum with midline raphe', 'XPO:0101567', 'abnormal tongue', 0.5423728813559322, 7.884497199543557, 2.0679307203480533, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(629953, 'HP:0011826', 'Philtrum with midline raphe', 'XPO:0103352', 'decreased size of the mouth', 0.47297297297297297, 7.884497199543557, 1.9311017790021312, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(629954, 'HP:0011826', 'Philtrum with midline raphe', 'XPO:0129225', 'decreased size of the upper jaw', 0.4186046511627907, 8.81758714901448, 1.9212191422663665, 'UPHENO:0087585', 'abnormal midface morphology'),
(629955, 'HP:0011826', 'Philtrum with midline raphe', 'XPO:0141009', 'abnormally necrotic oral epithelium', 0.4074074074074074, 7.312692920701687, 1.7260490329042149, 'UPHENO:0076800', 'abnormal mouth morphology'),
(629956, 'HP:0011826', 'Philtrum with midline raphe', 'XPO:0103828', 'decreased width of the mouth', 0.4430379746835443, 7.884497199543557, 1.8689921537245293, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(629957, 'HP:0011826', 'Philtrum with midline raphe', 'XPO:0115558', 'abnormally incomplete structure of mouth', 0.5, 7.312692920701687, 1.9121575406725366, 'UPHENO:0076800', 'abnormal mouth morphology'),
(629958, 'HP:0011826', 'Philtrum with midline raphe', 'XPO:0129585', 'increased size of the tongue', 0.42168674698795183, 7.884497199543557, 1.8234001139933984, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(629959, 'HP:0011826', 'Philtrum with midline raphe', 'XPO:0130628', 'increased size of the oral cavity', 0.5, 7.884497199543557, 1.9855096574360394, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(629960, 'HP:0011826', 'Philtrum with midline raphe', 'XPO:0103735', 'increased size of the mouth', 0.47297297297297297, 7.884497199543557, 1.9311017790021312, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(629961, 'HP:0031085', 'Decreased prealbumin level', 'XPO:0141873', 'abnormal tricarboxylic acid metabolic process', 0.4339622641509434, 7.41682187759612, 1.7940515084037758, 'HP:0430071', 'Abnormal circulating organic compound concentration'),
(629962, 'HP:0031085', 'Decreased prealbumin level', 'XPO:0141869', 'abnormal alpha-amino acid metabolic process', 0.40350877192982454, 7.41682187759612, 1.729957423594889, 'HP:0430071', 'Abnormal circulating organic compound concentration'),
(629963, 'HP:0001112', 'Leber optic atrophy', 'XPO:0130539', 'increased size of the ciliary body', 0.43529411764705883, 6.887869297006056, 1.7315452601963712, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(629964, 'HP:0001112', 'Leber optic atrophy', 'XPO:0129419', 'decreased size of the pupil', 0.43529411764705883, 6.887869297006056, 1.7315452601963712, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(629965, 'HP:0001112', 'Leber optic atrophy', 'XPO:0128807', 'decreased size of the lens transitional zone', 0.45121951219512196, 6.887869297006056, 1.7629353431872736, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(629966, 'HP:0001112', 'Leber optic atrophy', 'XPO:0129981', 'increased size of the retinal ganglion cell layer', 0.4673913043478261, 7.796308075334707, 1.9089071743875285, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(629967, 'HP:0001112', 'Leber optic atrophy', 'XPO:0140271', 'abnormally necrotic peripheral retina', 0.5443037974683544, 7.796308075334707, 2.0599903134815656, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(629968, 'HP:0001112', 'Leber optic atrophy', 'XPO:0141338', 'decreased pigmentation in the optic nerve', 0.46875, 10.917429094733171, 2.2621991265483623, 'HP:0000587', 'Abnormal optic nerve morphology'),
(629969, 'HP:0001112', 'Leber optic atrophy', 'XPO:0141014', 'abnormally necrotic retinal outer plexiform layer', 0.4725274725274725, 7.796308075334707, 1.9193670180253262, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(629970, 'HP:0001112', 'Leber optic atrophy', 'XPO:0141343', 'decreased pigmentation in the eye', 0.5138888888888888, 6.887869297006056, 1.8813823374982381, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(629971, 'HP:0001112', 'Leber optic atrophy', 'XPO:0103814', 'decreased length of axon in retinal ganglion cell', 0.4215686274509804, 7.796308075334707, 1.8129199912030998, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(629972, 'HP:0001112', 'Leber optic atrophy', 'XPO:0141337', 'increased pigmentation in the eye', 0.5138888888888888, 6.887869297006056, 1.8813823374982381, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(629973, 'HP:0001112', 'Leber optic atrophy', 'XPO:0128467', 'decreased size of the lens', 0.4567901234567901, 6.887869297006056, 1.773784278466136, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(629974, 'HP:0001112', 'Leber optic atrophy', 'XPO:0141141', 'abnormally necrotic cornea', 0.4457831325301205, 6.887869297006056, 1.7522830683646402, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(629975, 'HP:0001112', 'Leber optic atrophy', 'XPO:0140081', 'abnormally necrotic amacrine cell', 0.44329896907216493, 7.796308075334707, 1.859057646326458, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(629976, 'HP:0001112', 'Leber optic atrophy', 'XPO:0129580', 'increased size of the inner limiting membrane', 0.4673913043478261, 7.796308075334707, 1.9089071743875285, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(629977, 'HP:0001112', 'Leber optic atrophy', 'XPO:0128330', 'decreased size of the retinal progenitor cell region', 0.5443037974683544, 7.796308075334707, 2.0599903134815656, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(629978, 'HP:0001112', 'Leber optic atrophy', 'XPO:0102657', 'abnormal conjunctiva morphology', 0.4230769230769231, 6.575878401988876, 1.6679635490146203, 'UPHENO:0087924', 'abnormal camera-type eye morphology'),
(629979, 'HP:0001112', 'Leber optic atrophy', 'XPO:0101817', 'abnormal eye morphology', 0.5362318840579711, 6.887869297006056, 1.9218468019794424, 'HP:0012372', 'Abnormal eye morphology'),
(629980, 'HP:0001112', 'Leber optic atrophy', 'XPO:0102831', 'abnormal optic disc morphology', 0.5, 6.575878401988876, 1.8132675481005107, 'UPHENO:0087924', 'abnormal camera-type eye morphology'),
(629981, 'HP:0001112', 'Leber optic atrophy', 'XPO:0140538', 'abnormally necrotic optic disc', 0.4782608695652174, 6.575878401988876, 1.773410646942871, 'UPHENO:0087924', 'abnormal camera-type eye morphology'),
(629982, 'HP:0001112', 'Leber optic atrophy', 'XPO:0102196', 'abnormal central retina morphology', 0.6142857142857143, 7.796308075334707, 2.1884151056982915, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(629983, 'HP:0001112', 'Leber optic atrophy', 'XPO:0140218', 'abnormally necrotic sclera', 0.49333333333333335, 6.887869297006056, 1.8433706951821496, 'HP:0012372', 'Abnormal eye morphology'),
(629984, 'HP:0001112', 'Leber optic atrophy', 'XPO:0141323', 'edematous eye', 0.5211267605633803, 6.887869297006056, 1.8945851825486058, 'HP:0012372', 'Abnormal eye morphology'),
(629985, 'HP:0001112', 'Leber optic atrophy', 'XPO:0133372', 'eye fused with olfactory epithelium', 0.5138888888888888, 6.887869297006056, 1.8813823374982381, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(629986, 'HP:0001112', 'Leber optic atrophy', 'XPO:0130265', 'increased size of the peripheral retina', 0.5308641975308642, 7.796308075334707, 2.034399378223449, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(629987, 'HP:0001112', 'Leber optic atrophy', 'XPO:0130893', 'increased size of the pupil', 0.44047619047619047, 6.887869297006056, 1.741821583412935, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(629988, 'HP:0001112', 'Leber optic atrophy', 'XPO:0129810', 'increased size of the retinal progenitor cell region', 0.5443037974683544, 7.796308075334707, 2.0599903134815656, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(629989, 'HP:0001112', 'Leber optic atrophy', 'XPO:0128599', 'decreased size of the olfactory pit', 0.4057971014492754, 5.788671267106304, 1.532653261972336, 'UPHENO:0087472', 'abnormal face morphology'),
(629990, 'HP:0001112', 'Leber optic atrophy', 'XPO:0129681', 'increased size of the eye photoreceptor cell', 0.43434343434343436, 7.796308075334707, 1.8401834758089552, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(629991, 'HP:0001112', 'Leber optic atrophy', 'XPO:0128875', 'decreased size of the photoreceptor layer', 0.4725274725274725, 7.796308075334707, 1.9193670180253262, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(629992, 'HP:0001112', 'Leber optic atrophy', 'XPO:0130906', 'increased size of the retinal stem cell', 0.4479166666666667, 7.796308075334707, 1.8687151536310551, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(629993, 'HP:0001112', 'Leber optic atrophy', 'XPO:0130736', 'increased size of the cornea', 0.4157303370786517, 6.887869297006056, 1.6921868172864436, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(629994, 'HP:0001112', 'Leber optic atrophy', 'XPO:0102633', 'abnormal ventricular zone morphology', 0.40298507462686567, 5.483278994082134, 1.4864991068379805, 'HP:0002011', 'Morphological central nervous system abnormality'),
(629995, 'HP:0001112', 'Leber optic atrophy', 'XPO:0140439', 'abnormally necrotic retinal stem cell', 0.48863636363636365, 7.796308075334707, 1.9518093215579149, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(629996, 'HP:0001112', 'Leber optic atrophy', 'XPO:0140240', 'abnormally necrotic eye photoreceptor cell', 0.4725274725274725, 7.796308075334707, 1.9193670180253262, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(629997, 'HP:0001112', 'Leber optic atrophy', 'XPO:0130362', 'increased size of the retinal pigmented epithelium', 0.46236559139784944, 7.796308075334707, 1.8986164947065958, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(629998, 'HP:0001112', 'Leber optic atrophy', 'XPO:0128669', 'decreased size of the ciliary marginal zone', 0.48863636363636365, 7.796308075334707, 1.9518093215579149, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(629999, 'HP:0001112', 'Leber optic atrophy', 'XPO:0140869', 'abnormally necrotic optic chiasm', 0.5357142857142857, 10.917429094733171, 2.4183925920580682, 'HP:0000587', 'Abnormal optic nerve morphology'),
(630000, 'HP:0001112', 'Leber optic atrophy', 'XPO:0129955', 'increased size of the retinal stem cell region', 0.5443037974683544, 7.796308075334707, 2.0599903134815656, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(630001, 'HP:0001112', 'Leber optic atrophy', 'XPO:0130515', 'increased size of the retinal outer nuclear layer', 0.4673913043478261, 7.796308075334707, 1.9089071743875285, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(630002, 'HP:0001112', 'Leber optic atrophy', 'XPO:0140464', 'abnormally necrotic retinal pigmented epithelium', 0.4673913043478261, 7.796308075334707, 1.9089071743875285, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(630003, 'HP:0001112', 'Leber optic atrophy', 'XPO:0130863', 'increased size of the sclera', 0.4805194805194805, 6.887869297006056, 1.8192733100013945, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(630004, 'HP:0001112', 'Leber optic atrophy', 'XPO:0127563', 'abnormally localised retinal blood vessel', 0.5061728395061729, 7.796308075334707, 1.9865244514370002, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(630005, 'HP:0001112', 'Leber optic atrophy', 'XPO:0128521', 'decreased size of the horizontal cell', 0.42574257425742573, 7.796308075334707, 1.8218727369651686, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(630006, 'HP:0001112', 'Leber optic atrophy', 'XPO:0102963', 'abnormal retinal outer nuclear layer morphology', 0.5119047619047619, 7.796308075334707, 1.9977405309600107, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(630007, 'HP:0001112', 'Leber optic atrophy', 'XPO:0115423', 'abnormally incomplete structure of eye', 0.5285714285714286, 6.887869297006056, 1.9080699447692615, 'HP:0012372', 'Abnormal eye morphology'),
(630008, 'HP:0001112', 'Leber optic atrophy', 'XPO:0102232', 'abnormal eye photoreceptor cell morphology', 0.4942528735632184, 7.796308075334707, 1.962994566833618, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(630009, 'HP:0001112', 'Leber optic atrophy', 'XPO:0128568', 'decreased size of the optic disc', 0.4647887323943662, 6.575878401988876, 1.7482546115597408, 'UPHENO:0087924', 'abnormal camera-type eye morphology'),
(630010, 'HP:0001112', 'Leber optic atrophy', 'XPO:0103912', 'increased thickness of the optic nerve', 0.40540540540540543, 10.917429094733171, 2.1038024546366207, 'HP:0000587', 'Abnormal optic nerve morphology'),
(630011, 'HP:0001112', 'Leber optic atrophy', 'XPO:0102226', 'abnormal Jacobsons organ morphology', 0.42424242424242425, 5.788671267106304, 1.5670992092077785, 'UPHENO:0087472', 'abnormal face morphology'),
(630012, 'HP:0001112', 'Leber optic atrophy', 'XPO:0128100', 'decreased size of the inner limiting membrane', 0.4673913043478261, 7.796308075334707, 1.9089071743875285, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(630013, 'HP:0001112', 'Leber optic atrophy', 'XPO:0128501', 'decreased size of the retinal ganglion cell layer', 0.4673913043478261, 7.796308075334707, 1.9089071743875285, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(630014, 'HP:0001112', 'Leber optic atrophy', 'XPO:0141156', 'abnormally necrotic outer limiting membrane', 0.4725274725274725, 7.796308075334707, 1.9193670180253262, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(630015, 'HP:0001112', 'Leber optic atrophy', 'XPO:0140948', 'abnormally necrotic retinal inner nuclear layer', 0.4725274725274725, 7.796308075334707, 1.9193670180253262, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(630016, 'HP:0001112', 'Leber optic atrophy', 'XPO:0128787', 'decreased size of the peripheral retina', 0.5308641975308642, 7.796308075334707, 2.034399378223449, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(630017, 'HP:0001112', 'Leber optic atrophy', 'XPO:0133371', 'eye fused with olfactory pit', 0.5138888888888888, 6.887869297006056, 1.8813823374982381, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(630018, 'HP:0001112', 'Leber optic atrophy', 'XPO:0128646', 'decreased size of the outer limiting membrane', 0.4673913043478261, 7.796308075334707, 1.9089071743875285, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(630019, 'HP:0001112', 'Leber optic atrophy', 'XPO:0140553', 'abnormally necrotic retinal stem cell region', 0.5584415584415584, 7.796308075334707, 2.0865719330232593, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(630020, 'HP:0001112', 'Leber optic atrophy', 'XPO:0140820', 'abnormally necrotic globe', 0.4520547945205479, 6.575878401988876, 1.724139599859359, 'UPHENO:0087924', 'abnormal camera-type eye morphology'),
(630021, 'HP:0001112', 'Leber optic atrophy', 'XPO:0102851', 'abnormal retinal rod cell morphology', 0.48314606741573035, 7.796308075334707, 1.9408131252028016, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(630022, 'HP:0001112', 'Leber optic atrophy', 'XPO:0127566', 'abnormally localised hyaloid artery', 0.4157303370786517, 6.887869297006056, 1.6921868172864436, 'HP:0012372', 'Abnormal eye morphology'),
(630023, 'HP:0001112', 'Leber optic atrophy', 'XPO:0129260', 'decreased size of the cornea', 0.4157303370786517, 6.887869297006056, 1.6921868172864436, 'HP:0012372', 'Abnormal eye morphology'),
(630024, 'HP:0001112', 'Leber optic atrophy', 'XPO:0101861', 'abnormal photoreceptor layer morphology', 0.5180722891566265, 7.796308075334707, 2.0097390804676474, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(630025, 'HP:0001112', 'Leber optic atrophy', 'XPO:0102017', 'abnormal retinal neural layer morphology', 0.5180722891566265, 7.796308075334707, 2.0097390804676474, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(630026, 'HP:0001112', 'Leber optic atrophy', 'XPO:0140346', 'abnormally necrotic retinal blood vessel', 0.4270833333333333, 7.796308075334707, 1.8247392253435917, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(630027, 'HP:0001112', 'Leber optic atrophy', 'XPO:0130148', 'increased size of the ciliary marginal zone', 0.48863636363636365, 7.796308075334707, 1.9518093215579149, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(630028, 'HP:0001112', 'Leber optic atrophy', 'XPO:0103210', 'abnormal pupil morphology', 0.46835443037974683, 6.887869297006056, 1.796096907499542, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(630029, 'HP:0001112', 'Leber optic atrophy', 'XPO:0102441', 'abnormal retinal inner plexiform layer morphology', 0.5119047619047619, 7.796308075334707, 1.9977405309600107, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(630030, 'HP:0001112', 'Leber optic atrophy', 'XPO:0103142', 'abnormal optic nerve morphology', 0.4838709677419355, 10.917429094733171, 2.2983966109708964, 'HP:0000587', 'Abnormal optic nerve morphology'),
(630031, 'HP:0001112', 'Leber optic atrophy', 'XPO:0140391', 'abnormally necrotic central retina', 0.589041095890411, 7.796308075334707, 2.1429759337413046, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(630032, 'HP:0001112', 'Leber optic atrophy', 'XPO:0102882', 'abnormal retinal cone cell morphology', 0.48314606741573035, 7.796308075334707, 1.9408131252028016, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(630033, 'HP:0001112', 'Leber optic atrophy', 'XPO:0129138', 'decreased size of the retinal progenitor cell', 0.4479166666666667, 7.796308075334707, 1.8687151536310551, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(630034, 'HP:0001112', 'Leber optic atrophy', 'XPO:0128643', 'decreased size of the retinal layer', 0.5324675324675324, 7.796308075334707, 2.037469244732339, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(630035, 'HP:0001112', 'Leber optic atrophy', 'XPO:0103160', 'abnormal choroid morphology', 0.4714285714285714, 6.575878401988876, 1.7606978619108995, 'UPHENO:0087924', 'abnormal camera-type eye morphology'),
(630036, 'HP:0001112', 'Leber optic atrophy', 'XPO:0133354', 'fused eyes', 0.5138888888888888, 6.887869297006056, 1.8813823374982381, 'HP:0012372', 'Abnormal eye morphology'),
(630037, 'HP:0001112', 'Leber optic atrophy', 'XPO:0140375', 'abnormally necrotic lens', 0.47435897435897434, 6.887869297006056, 1.8075736818305534, 'HP:0012372', 'Abnormal eye morphology'),
(630038, 'HP:0001112', 'Leber optic atrophy', 'XPO:0140250', 'abnormally necrotic iris', 0.44047619047619047, 6.887869297006056, 1.741821583412935, 'HP:0012372', 'Abnormal eye morphology'),
(630039, 'HP:0001112', 'Leber optic atrophy', 'XPO:0100710', 'abnormal hyaloid vein', 0.4492753623188406, 6.887869297006056, 1.759133301946505, 'HP:0012372', 'Abnormal eye morphology'),
(630040, 'HP:0001112', 'Leber optic atrophy', 'XPO:0140452', 'abnormally necrotic lens epithelium', 0.4111111111111111, 6.887869297006056, 1.6827595193254048, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(630041, 'HP:0001112', 'Leber optic atrophy', 'XPO:0103706', 'increased pigmentation in the optic nerve', 0.46875, 10.917429094733171, 2.2621991265483623, 'HP:0000587', 'Abnormal optic nerve morphology'),
(630042, 'HP:0001112', 'Leber optic atrophy', 'XPO:0129532', 'increased size of the iris', 0.43023255813953487, 6.887869297006056, 1.7214487003049714, 'HP:0012372', 'Abnormal eye morphology'),
(630043, 'HP:0001112', 'Leber optic atrophy', 'XPO:0103184', 'abnormal inner limiting membrane morphology', 0.5119047619047619, 7.796308075334707, 1.9977405309600107, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(630044, 'HP:0001112', 'Leber optic atrophy', 'XPO:0103226', 'abnormal retinal outer plexiform layer morphology', 0.5119047619047619, 7.796308075334707, 1.9977405309600107, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(630045, 'HP:0001112', 'Leber optic atrophy', 'XPO:0130761', 'increased size of the retinal inner plexiform layer', 0.4673913043478261, 7.796308075334707, 1.9089071743875285, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(630046, 'HP:0001112', 'Leber optic atrophy', 'XPO:0102966', 'abnormal olfactory pit morphology', 0.4375, 5.788671267106304, 1.5913967699348293, 'UPHENO:0087472', 'abnormal face morphology'),
(630047, 'HP:0001112', 'Leber optic atrophy', 'XPO:0102996', 'abnormal optic fiber layer morphology', 0.5119047619047619, 7.796308075334707, 1.9977405309600107, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(630048, 'HP:0001112', 'Leber optic atrophy', 'XPO:0103336', 'decreased size of the eye', 0.4625, 6.887869297006056, 1.7848360008318136, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(630049, 'HP:0001112', 'Leber optic atrophy', 'XPO:0129432', 'decreased size of the retinal stem cell', 0.4479166666666667, 7.796308075334707, 1.8687151536310551, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(630050, 'HP:0001112', 'Leber optic atrophy', 'XPO:0130122', 'increased size of the retinal layer', 0.5324675324675324, 7.796308075334707, 2.037469244732339, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(630051, 'HP:0001112', 'Leber optic atrophy', 'XPO:0102805', 'abnormal retinal layer morphology', 0.5857142857142857, 7.796308075334707, 2.1369157717498335, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(630052, 'HP:0001112', 'Leber optic atrophy', 'XPO:0140547', 'abnormally necrotic lower eyelid', 0.4024390243902439, 6.575878401988876, 1.6267729062795704, 'UPHENO:0087924', 'abnormal camera-type eye morphology'),
(630053, 'HP:0001112', 'Leber optic atrophy', 'XPO:0129971', 'increased size of the retinal ganglion cell', 0.4174757281553398, 7.796308075334707, 1.8040979437585178, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(630054, 'HP:0001112', 'Leber optic atrophy', 'XPO:0102541', 'abnormal choroid fissure morphology', 0.4024390243902439, 6.575878401988876, 1.6267729062795704, 'UPHENO:0087924', 'abnormal camera-type eye morphology'),
(630055, 'HP:0001112', 'Leber optic atrophy', 'XPO:0102663', 'abnormal retinal progenitor cell morphology', 0.5180722891566265, 7.796308075334707, 2.0097390804676474, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(630056, 'HP:0001112', 'Leber optic atrophy', 'XPO:0140797', 'abnormally necrotic bipolar neuron', 0.44329896907216493, 7.796308075334707, 1.859057646326458, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(630057, 'HP:0001112', 'Leber optic atrophy', 'XPO:0129780', 'increased size of the retina', 0.5584415584415584, 7.796308075334707, 2.0865719330232593, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(630058, 'HP:0001112', 'Leber optic atrophy', 'XPO:0130189', 'increased size of the optic chiasm', 0.5113636363636364, 10.917429094733171, 2.362789927527396, 'HP:0000587', 'Abnormal optic nerve morphology'),
(630059, 'HP:0001112', 'Leber optic atrophy', 'XPO:0102411', 'abnormal optic choroid vascular plexus morphology', 0.4111111111111111, 7.796308075334707, 1.7902929579863123, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(630060, 'HP:0001112', 'Leber optic atrophy', 'XPO:0140006', 'abnormally necrotic retinal neural layer', 0.4725274725274725, 7.796308075334707, 1.9193670180253262, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(630061, 'HP:0001112', 'Leber optic atrophy', 'XPO:0102784', 'abnormal retinal progenitor cell region morphology', 0.581081081081081, 7.796308075334707, 2.1284471158233305, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(630062, 'HP:0001112', 'Leber optic atrophy', 'XPO:0102550', 'abnormal lens morphology', 0.5068493150684932, 6.887869297006056, 1.8684517214712355, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(630063, 'HP:0001112', 'Leber optic atrophy', 'XPO:0103086', 'abnormal amacrine cell morphology', 0.4725274725274725, 7.796308075334707, 1.9193670180253262, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(630064, 'HP:0001112', 'Leber optic atrophy', 'XPO:0103110', 'abnormal lens fiber cell mass morphology', 0.43529411764705883, 6.887869297006056, 1.7315452601963712, 'HP:0012372', 'Abnormal eye morphology'),
(630065, 'HP:0001112', 'Leber optic atrophy', 'XPO:0102239', 'abnormal retinal pigmented epithelium morphology', 0.5119047619047619, 7.796308075334707, 1.9977405309600107, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(630066, 'HP:0001112', 'Leber optic atrophy', 'XPO:0129258', 'decreased size of the amacrine cell', 0.4095238095238095, 7.796308075334707, 1.786833451453243, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(630067, 'HP:0001112', 'Leber optic atrophy', 'XPO:0128848', 'decreased size of the retinal cone cell', 0.4215686274509804, 7.796308075334707, 1.8129199912030998, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(630068, 'HP:0001112', 'Leber optic atrophy', 'XPO:0130048', 'increased size of the optic disc', 0.4647887323943662, 6.575878401988876, 1.7482546115597408, 'UPHENO:0087924', 'abnormal camera-type eye morphology'),
(630069, 'HP:0001112', 'Leber optic atrophy', 'XPO:0103048', 'abnormal cornea morphology', 0.4805194805194805, 6.887869297006056, 1.8192733100013945, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(630070, 'HP:0001112', 'Leber optic atrophy', 'XPO:0140808', 'abnormally necrotic retinal cone cell', 0.4574468085106383, 7.796308075334707, 1.8884904678678098, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(630071, 'HP:0001112', 'Leber optic atrophy', 'XPO:0130396', 'increased size of the choroid', 0.42857142857142855, 6.575878401988876, 1.6787595422967447, 'UPHENO:0087924', 'abnormal camera-type eye morphology'),
(630072, 'HP:0001112', 'Leber optic atrophy', 'XPO:0139912', 'abnormally necrotic optic fiber layer', 0.4725274725274725, 7.796308075334707, 1.9193670180253262, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(630073, 'HP:0001112', 'Leber optic atrophy', 'XPO:0102756', 'abnormal Muller cell morphology', 0.5512820512820513, 7.796308075334707, 2.0731533248164107, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(630074, 'HP:0001112', 'Leber optic atrophy', 'XPO:0129947', 'increased size of the lens', 0.4567901234567901, 6.887869297006056, 1.773784278466136, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(630075, 'HP:0001112', 'Leber optic atrophy', 'XPO:0130326', 'increased size of the retinal cone cell', 0.4215686274509804, 7.796308075334707, 1.8129199912030998, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(630076, 'HP:0001112', 'Leber optic atrophy', 'XPO:0107252', 'decreased size of the globe', 0.44, 6.575878401988876, 1.700995736877405, 'UPHENO:0087924', 'abnormal camera-type eye morphology'),
(630077, 'HP:0001112', 'Leber optic atrophy', 'XPO:0129911', 'increased size of the retinal inner nuclear layer', 0.4673913043478261, 7.796308075334707, 1.9089071743875285, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(630078, 'HP:0001112', 'Leber optic atrophy', 'XPO:0129388', 'decreased size of the sclera', 0.4805194805194805, 6.887869297006056, 1.8192733100013945, 'HP:0012372', 'Abnormal eye morphology'),
(630079, 'HP:0001112', 'Leber optic atrophy', 'XPO:0140671', 'abnormally necrotic retinal ganglion cell', 0.45263157894736844, 7.796308075334707, 1.8785247493974806, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(630080, 'HP:0001112', 'Leber optic atrophy', 'XPO:0140799', 'abnormally necrotic ciliary body', 0.4457831325301205, 6.887869297006056, 1.7522830683646402, 'HP:0012372', 'Abnormal eye morphology'),
(630081, 'HP:0001112', 'Leber optic atrophy', 'XPO:0102505', 'abnormal retinal stem cell region morphology', 0.581081081081081, 7.796308075334707, 2.1284471158233305, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(630082, 'HP:0001112', 'Leber optic atrophy', 'XPO:0140489', 'abnormally necrotic ciliary marginal zone', 0.5, 7.796308075334707, 1.9743743408146677, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(630083, 'HP:0001112', 'Leber optic atrophy', 'XPO:0130125', 'increased size of the outer limiting membrane', 0.4673913043478261, 7.796308075334707, 1.9089071743875285, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(630084, 'HP:0001112', 'Leber optic atrophy', 'XPO:0141033', 'abnormally necrotic photoreceptor layer', 0.4777777777777778, 7.796308075334707, 1.9300007116849363, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(630085, 'HP:0001112', 'Leber optic atrophy', 'XPO:0128431', 'decreased size of the retinal inner nuclear layer', 0.4673913043478261, 7.796308075334707, 1.9089071743875285, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(630086, 'HP:0001112', 'Leber optic atrophy', 'XPO:0102939', 'abnormal retinal ganglion cell layer morphology', 0.5119047619047619, 7.796308075334707, 1.9977405309600107, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(630087, 'HP:0001112', 'Leber optic atrophy', 'XPO:0100329', 'abnormal retinal blood vessel', 0.5774647887323944, 7.796308075334707, 2.121813704267134, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(630088, 'HP:0001112', 'Leber optic atrophy', 'XPO:0130169', 'increased size of the optic nerve', 0.4205607476635514, 10.917429094733171, 2.1427650694009346, 'HP:0000587', 'Abnormal optic nerve morphology'),
(630089, 'HP:0001112', 'Leber optic atrophy', 'XPO:0130285', 'increased size of the lens transitional zone', 0.45121951219512196, 6.887869297006056, 1.7629353431872736, 'HP:0012372', 'Abnormal eye morphology'),
(630090, 'HP:0001112', 'Leber optic atrophy', 'XPO:0103186', 'abnormal peripheral retina morphology', 0.589041095890411, 7.796308075334707, 2.1429759337413046, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(630091, 'HP:0001112', 'Leber optic atrophy', 'XPO:0102450', 'abnormal retinal stem cell morphology', 0.5180722891566265, 7.796308075334707, 2.0097390804676474, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(630092, 'HP:0001112', 'Leber optic atrophy', 'XPO:0101359', 'abnormal hyaloid artery', 0.4805194805194805, 6.887869297006056, 1.8192733100013945, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(630093, 'HP:0001112', 'Leber optic atrophy', 'XPO:0130845', 'increased size of the retinal outer plexiform layer', 0.4673913043478261, 7.796308075334707, 1.9089071743875285, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(630094, 'HP:0001112', 'Leber optic atrophy', 'XPO:0130506', 'increased size of the Muller cell', 0.4725274725274725, 7.796308075334707, 1.9193670180253262, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(630095, 'HP:0001112', 'Leber optic atrophy', 'XPO:0140520', 'abnormally necrotic retinal outer nuclear layer', 0.4725274725274725, 7.796308075334707, 1.9193670180253262, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(630096, 'HP:0001112', 'Leber optic atrophy', 'XPO:0129741', 'increased size of the optic fiber layer', 0.4673913043478261, 7.796308075334707, 1.9089071743875285, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(630097, 'HP:0001112', 'Leber optic atrophy', 'XPO:0102818', 'abnormal optic chiasm morphology', 0.569620253164557, 10.917429094733171, 2.493749932300352, 'HP:0000587', 'Abnormal optic nerve morphology'),
(630098, 'HP:0001112', 'Leber optic atrophy', 'XPO:0141333', 'increased pigmentation in the retinal pigmented epithelium', 0.4942528735632184, 7.796308075334707, 1.962994566833618, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(630099, 'HP:0001112', 'Leber optic atrophy', 'XPO:0130734', 'increased size of the amacrine cell', 0.4095238095238095, 7.796308075334707, 1.786833451453243, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(630100, 'HP:0001112', 'Leber optic atrophy', 'XPO:0102815', 'abnormal retinal ganglion cell morphology', 0.4777777777777778, 7.796308075334707, 1.9300007116849363, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(630101, 'HP:0001112', 'Leber optic atrophy', 'XPO:0129038', 'decreased size of the retinal outer nuclear layer', 0.4673913043478261, 7.796308075334707, 1.9089071743875285, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(630102, 'HP:0001112', 'Leber optic atrophy', 'XPO:0141182', 'abnormally necrotic inner limiting membrane', 0.4725274725274725, 7.796308075334707, 1.9193670180253262, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(630103, 'HP:0001112', 'Leber optic atrophy', 'XPO:0102946', 'abnormal retinal inner nuclear layer morphology', 0.5119047619047619, 7.796308075334707, 1.9977405309600107, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(630104, 'HP:0001112', 'Leber optic atrophy', 'XPO:0102266', 'abnormal horizontal cell morphology', 0.48863636363636365, 7.796308075334707, 1.9518093215579149, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(630105, 'HP:0001112', 'Leber optic atrophy', 'XPO:0100779', 'abnormal optic choroid vascular plexus', 0.45588235294117646, 6.887869297006056, 1.7720208976957377, 'HP:0012372', 'Abnormal eye morphology'),
(630106, 'HP:0001112', 'Leber optic atrophy', 'XPO:0128200', 'decreased size of the retinal rod cell', 0.4215686274509804, 7.796308075334707, 1.8129199912030998, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(630107, 'HP:0001112', 'Leber optic atrophy', 'XPO:0129083', 'decreased size of the bipolar neuron', 0.4095238095238095, 7.796308075334707, 1.786833451453243, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(630108, 'HP:0001112', 'Leber optic atrophy', 'XPO:0101823', 'abnormal lens epithelium morphology', 0.45121951219512196, 6.887869297006056, 1.7629353431872736, 'HP:0012372', 'Abnormal eye morphology'),
(630109, 'HP:0001112', 'Leber optic atrophy', 'XPO:0103155', 'abnormal bipolar neuron morphology', 0.4725274725274725, 7.796308075334707, 1.9193670180253262, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(630110, 'HP:0001112', 'Leber optic atrophy', 'XPO:0129680', 'increased size of the retinal rod cell', 0.4215686274509804, 7.796308075334707, 1.8129199912030998, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(630111, 'HP:0001112', 'Leber optic atrophy', 'XPO:0140491', 'abnormally necrotic retinal rod cell', 0.4574468085106383, 7.796308075334707, 1.8884904678678098, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(630112, 'HP:0001112', 'Leber optic atrophy', 'XPO:0103376', 'increased size of the eye', 0.4625, 6.887869297006056, 1.7848360008318136, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(630113, 'HP:0001112', 'Leber optic atrophy', 'XPO:0140531', 'abnormally necrotic retinal progenitor cell region', 0.5584415584415584, 7.796308075334707, 2.0865719330232593, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(630114, 'HP:0001112', 'Leber optic atrophy', 'XPO:0128779', 'decreased size of the retinal blood vessel', 0.41836734693877553, 7.796308075334707, 1.8060234564908433, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(630115, 'HP:0001112', 'Leber optic atrophy', 'XPO:0102723', 'abnormal lower eyelid morphology', 0.4342105263157895, 6.575878401988876, 1.689767919542865, 'UPHENO:0087924', 'abnormal camera-type eye morphology'),
(630116, 'HP:0001112', 'Leber optic atrophy', 'XPO:0102476', 'abnormal lens transitional zone morphology', 0.49333333333333335, 6.887869297006056, 1.8433706951821496, 'HP:0012372', 'Abnormal eye morphology'),
(630117, 'HP:0001112', 'Leber optic atrophy', 'XPO:0127230', 'abnormally localised hyaloid blood vessel', 0.40789473684210525, 6.887869297006056, 1.6761639640277146, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(630118, 'HP:0001112', 'Leber optic atrophy', 'XPO:0139731', 'abnormally necrotic eye', 0.4868421052631579, 6.887869297006056, 1.8312030988756807, 'HP:0012372', 'Abnormal eye morphology'),
(630119, 'HP:0001112', 'Leber optic atrophy', 'XPO:0129062', 'decreased size of the ciliary body', 0.43529411764705883, 6.887869297006056, 1.7315452601963712, 'HP:0012372', 'Abnormal eye morphology'),
(630120, 'HP:0001112', 'Leber optic atrophy', 'XPO:0103926', 'decreased pigmentation in the retinal pigmented epithelium', 0.4942528735632184, 7.796308075334707, 1.962994566833618, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(630121, 'HP:0001112', 'Leber optic atrophy', 'XPO:0128710', 'decreased size of the optic chiasm', 0.5113636363636364, 10.917429094733171, 2.362789927527396, 'HP:0000587', 'Abnormal optic nerve morphology'),
(630122, 'HP:0001112', 'Leber optic atrophy', 'XPO:0129775', 'increased size of the retinal neural layer', 0.4673913043478261, 7.796308075334707, 1.9089071743875285, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(630123, 'HP:0001112', 'Leber optic atrophy', 'XPO:0128884', 'decreased size of the retinal pigmented epithelium', 0.46236559139784944, 7.796308075334707, 1.8986164947065958, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(630124, 'HP:0001112', 'Leber optic atrophy', 'XPO:0128261', 'decreased size of the optic fiber layer', 0.4673913043478261, 7.796308075334707, 1.9089071743875285, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(630125, 'HP:0001112', 'Leber optic atrophy', 'XPO:0101315', 'abnormal hyaloid vascular plexus', 0.4492753623188406, 6.887869297006056, 1.759133301946505, 'HP:0012372', 'Abnormal eye morphology'),
(630126, 'HP:0001112', 'Leber optic atrophy', 'XPO:0102212', 'abnormal globe morphology', 0.4852941176470588, 6.575878401988876, 1.7864028400244842, 'UPHENO:0087924', 'abnormal camera-type eye morphology'),
(630127, 'HP:0001112', 'Leber optic atrophy', 'XPO:0141181', 'abnormally necrotic choroid', 0.44, 6.575878401988876, 1.700995736877405, 'UPHENO:0087924', 'abnormal camera-type eye morphology'),
(630128, 'HP:0001112', 'Leber optic atrophy', 'XPO:0128918', 'decreased size of the choroid', 0.42857142857142855, 6.575878401988876, 1.6787595422967447, 'UPHENO:0087924', 'abnormal camera-type eye morphology'),
(630129, 'HP:0001112', 'Leber optic atrophy', 'XPO:0133369', 'eye fused with brain', 0.5138888888888888, 6.887869297006056, 1.8813823374982381, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(630130, 'HP:0001112', 'Leber optic atrophy', 'XPO:0130353', 'increased size of the photoreceptor layer', 0.4725274725274725, 7.796308075334707, 1.9193670180253262, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(630131, 'HP:0001112', 'Leber optic atrophy', 'XPO:0128935', 'decreased size of the central retina', 0.5733333333333334, 7.796308075334707, 2.114209851581728, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(630132, 'HP:0001112', 'Leber optic atrophy', 'XPO:0125909', 'absent retinal blood vessel', 0.47674418604651164, 7.796308075334707, 1.9279119657140185, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(630133, 'HP:0001112', 'Leber optic atrophy', 'XPO:0140945', 'abnormally necrotic retinal ganglion cell layer', 0.4725274725274725, 7.796308075334707, 1.9193670180253262, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(630134, 'HP:0001112', 'Leber optic atrophy', 'XPO:0129285', 'decreased size of the retinal inner plexiform layer', 0.4673913043478261, 7.796308075334707, 1.9089071743875285, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(630135, 'HP:0001112', 'Leber optic atrophy', 'XPO:0102513', 'abnormal sclera morphology', 0.5285714285714286, 6.887869297006056, 1.9080699447692615, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(630136, 'HP:0001112', 'Leber optic atrophy', 'XPO:0130651', 'increased size of the lens epithelium', 0.40217391304347827, 6.887869297006056, 1.6643681526960787, 'HP:0012372', 'Abnormal eye morphology'),
(630137, 'HP:0001112', 'Leber optic atrophy', 'XPO:0100371', 'abnormal hyaloid blood vessel', 0.4626865671641791, 6.887869297006056, 1.7851959556606887, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(630138, 'HP:0001112', 'Leber optic atrophy', 'XPO:0140487', 'abnormally necrotic retinal layer', 0.5394736842105263, 7.796308075334707, 2.0508298419520554, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(630139, 'HP:0001112', 'Leber optic atrophy', 'XPO:0128690', 'decreased size of the optic nerve', 0.42857142857142855, 10.917429094733171, 2.1630760928495034, 'HP:0000587', 'Abnormal optic nerve morphology'),
(630140, 'HP:0001112', 'Leber optic atrophy', 'XPO:0102581', 'abnormal outer limiting membrane morphology', 0.5119047619047619, 7.796308075334707, 1.9977405309600107, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(630141, 'HP:0001112', 'Leber optic atrophy', 'XPO:0130079', 'increased size of the olfactory pit', 0.4057971014492754, 5.788671267106304, 1.532653261972336, 'UPHENO:0087472', 'abnormal face morphology'),
(630142, 'HP:0001112', 'Leber optic atrophy', 'XPO:0129029', 'decreased size of the Muller cell', 0.4725274725274725, 7.796308075334707, 1.9193670180253262, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(630143, 'HP:0001112', 'Leber optic atrophy', 'XPO:0129371', 'decreased size of the retinal outer plexiform layer', 0.4673913043478261, 7.796308075334707, 1.9089071743875285, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(630144, 'HP:0001112', 'Leber optic atrophy', 'XPO:0140620', 'abnormally necrotic horizontal cell', 0.46236559139784944, 7.796308075334707, 1.8986164947065958, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(630145, 'HP:0001112', 'Leber optic atrophy', 'XPO:0128491', 'decreased size of the retinal ganglion cell', 0.4174757281553398, 7.796308075334707, 1.8040979437585178, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(630146, 'HP:0001112', 'Leber optic atrophy', 'XPO:0128475', 'decreased size of the retinal stem cell region', 0.5443037974683544, 7.796308075334707, 2.0599903134815656, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(630147, 'HP:0001112', 'Leber optic atrophy', 'XPO:0115417', 'abnormally wholly ventralized eye', 0.4868421052631579, 6.887869297006056, 1.8312030988756807, 'HP:0012372', 'Abnormal eye morphology'),
(630148, 'HP:0001112', 'Leber optic atrophy', 'XPO:0103022', 'abnormal ciliary body morphology', 0.4805194805194805, 6.887869297006056, 1.8192733100013945, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(630149, 'HP:0001112', 'Leber optic atrophy', 'XPO:0139887', 'abnormally necrotic Muller cell', 0.5180722891566265, 7.796308075334707, 2.0097390804676474, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(630150, 'HP:0001112', 'Leber optic atrophy', 'XPO:0130257', 'increased size of the retinal blood vessel', 0.41836734693877553, 7.796308075334707, 1.8060234564908433, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(630151, 'HP:0001112', 'Leber optic atrophy', 'XPO:0130614', 'increased size of the retinal progenitor cell', 0.4479166666666667, 7.796308075334707, 1.8687151536310551, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(630152, 'HP:0001112', 'Leber optic atrophy', 'XPO:0133370', 'olfactory pit fused with brain', 0.417910447761194, 5.788671267106304, 1.5553604730668558, 'UPHENO:0087472', 'abnormal face morphology'),
(630153, 'HP:0001112', 'Leber optic atrophy', 'XPO:0130859', 'increased size of the globe', 0.44, 6.575878401988876, 1.700995736877405, 'UPHENO:0087924', 'abnormal camera-type eye morphology'),
(630154, 'HP:0001112', 'Leber optic atrophy', 'XPO:0129175', 'decreased size of the lens epithelium', 0.40217391304347827, 6.887869297006056, 1.6643681526960787, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(630155, 'HP:0001112', 'Leber optic atrophy', 'XPO:0130560', 'increased size of the bipolar neuron', 0.4095238095238095, 7.796308075334707, 1.786833451453243, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(630156, 'HP:0001112', 'Leber optic atrophy', 'XPO:0140192', 'abnormally necrotic retina', 0.5733333333333334, 7.796308075334707, 2.114209851581728, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(630157, 'HP:0001112', 'Leber optic atrophy', 'XPO:0140435', 'abnormally necrotic optic nerve', 0.4411764705882353, 10.917429094733171, 2.1946555164562143, 'HP:0000587', 'Abnormal optic nerve morphology'),
(630158, 'HP:0001112', 'Leber optic atrophy', 'XPO:0128295', 'decreased size of the retinal neural layer', 0.4673913043478261, 7.796308075334707, 1.9089071743875285, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(630159, 'HP:0001112', 'Leber optic atrophy', 'XPO:0140473', 'abnormally necrotic lens transitional zone', 0.4625, 6.887869297006056, 1.7848360008318136, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(630160, 'HP:0001112', 'Leber optic atrophy', 'XPO:0128052', 'decreased size of the iris', 0.43023255813953487, 6.887869297006056, 1.7214487003049714, 'HP:0012372', 'Abnormal eye morphology'),
(630161, 'HP:0001112', 'Leber optic atrophy', 'XPO:0141638', 'neoplastic eye', 0.5138888888888888, 6.887869297006056, 1.8813823374982381, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(630162, 'HP:0001112', 'Leber optic atrophy', 'XPO:0141138', 'abnormally necrotic retinal inner plexiform layer', 0.4725274725274725, 7.796308075334707, 1.9193670180253262, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(630163, 'HP:0001112', 'Leber optic atrophy', 'XPO:0102862', 'abnormal iris morphology', 0.46835443037974683, 6.887869297006056, 1.796096907499542, 'HP:0012372', 'Abnormal eye morphology'),
(630164, 'HP:0001112', 'Leber optic atrophy', 'XPO:0130413', 'increased size of the central retina', 0.5733333333333334, 7.796308075334707, 2.114209851581728, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(630165, 'HP:0001112', 'Leber optic atrophy', 'XPO:0130001', 'increased size of the horizontal cell', 0.42574257425742573, 7.796308075334707, 1.8218727369651686, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(630166, 'HP:0001112', 'Leber optic atrophy', 'XPO:0102117', 'abnormal retina morphology', 0.6142857142857143, 7.796308075334707, 2.1884151056982915, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(630167, 'HP:0001112', 'Leber optic atrophy', 'XPO:0101961', 'abnormal retinal blood vessel morphology', 0.4606741573033708, 7.796308075334707, 1.8951405363936156, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(630168, 'HP:0001112', 'Leber optic atrophy', 'XPO:0128300', 'decreased size of the retina', 0.5584415584415584, 7.796308075334707, 2.0865719330232593, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(630169, 'HP:0001112', 'Leber optic atrophy', 'XPO:0128201', 'decreased size of the eye photoreceptor cell', 0.43434343434343436, 7.796308075334707, 1.8401834758089552, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(630170, 'HP:0001112', 'Leber optic atrophy', 'XPO:0102162', 'abnormal ciliary marginal zone morphology', 0.5512820512820513, 7.796308075334707, 2.0731533248164107, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(630171, 'HP:0001112', 'Leber optic atrophy', 'XPO:0140317', 'abnormally necrotic retinal progenitor cell', 0.48863636363636365, 7.796308075334707, 1.9518093215579149, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(630172, 'HP:0031997', 'Early inspiratory crackles', 'XPO:0101543', 'abnormal external gill', 0.40625, 6.780552239366747, 1.6596985711998251, 'UPHENO:0004536', 'abnormal respiratory system'),
(630173, 'HP:0031997', 'Early inspiratory crackles', 'XPO:0101949', 'abnormal respiratory system morphology', 0.47368421052631576, 7.032762738978795, 1.825187296096502, 'HP:0002795', 'Abnormal respiratory system physiology'),
(630174, 'HP:0031997', 'Early inspiratory crackles', 'XPO:0100317', 'abnormal respiratory system', 0.4642857142857143, 6.780552239366747, 1.7742924053565663, 'UPHENO:0004536', 'abnormal respiratory system'),
(630175, 'HP:0031997', 'Early inspiratory crackles', 'XPO:0139850', 'abnormally necrotic respiratory system', 0.4186046511627907, 7.032762738978795, 1.7157934587417247, 'UPHENO:0002448', 'abnormality of respiratory system physiology'),
(630176, 'HP:0031997', 'Early inspiratory crackles', 'XPO:0100804', 'abnormal larynx', 0.4186046511627907, 7.032762738978795, 1.7157934587417247, 'UPHENO:0002448', 'abnormality of respiratory system physiology'),
(630177, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100293', 'abnormal duct', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630178, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100484', 'abnormal cement gland primordium', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630179, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0101141', 'abnormal Keller explant', 0.5294117647058824, 1.706362323152461, 0.9504568842024205, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630180, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100722', 'abnormal barbel', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630181, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100438', 'abnormal spinal cord', 0.5, 3.94131651835137, 1.4038013602984167, 'UPHENO:0004523', 'abnormal nervous system'),
(630182, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0107284', 'abnormal migrating myoblast', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(630183, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0101057', 'abnormal vegetal pole', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630184, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0101221', 'abnormal larval immune system', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(630185, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100537', 'abnormal medium cavity', 0.5416666666666666, 3.94131651835137, 1.46112278086876, 'UPHENO:0004523', 'abnormal nervous system'),
(630186, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100533', 'abnormal melanoblast', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(630187, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100218', 'abnormal epithelial cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(630188, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100868', 'abnormal transporting epithelium', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630189, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0126321', 'abnormally localised anatomical structure', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630190, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100863', 'abnormal spinal neuron', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(630191, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0101498', 'abnormal stage II oocyte', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(630192, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0142052', 'abnormal nasal region', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(630193, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0101378', 'abnormal blastomere D1', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(630194, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0126485', 'abnormally localised olfactory system', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(630195, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100540', 'abnormal left lymph heart', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(630196, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100969', 'abnormal disaggregated/reaggregated ectoderm treated with activin', 0.5294117647058824, 1.706362323152461, 0.9504568842024205, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630197, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0101976', 'abnormal portion of organism substance morphology', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630198, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100319', 'abnormal middle lateral line', 0.5, 6.642668884102504, 1.8224528641507445, 'HP:0410008', 'Abnormality of the peripheral nervous system'),
(630199, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0101577', 'abnormal notochordal epithelium', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630200, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100643', 'abnormal thoracic region', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630201, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0107265', 'abnormal posterior side', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630202, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0141771', 'abnormal urea homeostasis', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(630203, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0107266', 'abnormal dorsal side', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630204, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0101228', 'abnormal mesenchymal stem cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(630205, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0101271', 'abnormal roof plate', 0.4642857142857143, 3.94131651835137, 1.3527368387638634, 'UPHENO:0004523', 'abnormal nervous system'),
(630206, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0141792', 'abnormal small molecule metabolic process', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(630207, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0142057', 'abnormal desmosome', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(630208, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0101480', 'abnormal stage V oocyte', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(630209, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100256', 'abnormal paired appendage', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630210, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0101461', 'abnormal sperm entry point', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(630211, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100493', 'abnormal liver and biliary system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(630212, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0124819', 'absent peripheral nervous system', 0.4117647058823529, 6.642668884102504, 1.653849025557147, 'HP:0410008', 'Abnormality of the peripheral nervous system'),
(630213, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0101110', 'abnormal cell-free extract', 0.5294117647058824, 1.706362323152461, 0.9504568842024205, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630214, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0107270', 'abnormal proximal-distal axis', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630215, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0101234', 'abnormal gasserian ganglion', 0.4117647058823529, 6.642668884102504, 1.653849025557147, 'HP:0410008', 'Abnormality of the peripheral nervous system'),
(630216, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0101426', 'abnormal dorsal funiculus', 0.4642857142857143, 3.94131651835137, 1.3527368387638634, 'UPHENO:0004523', 'abnormal nervous system'),
(630217, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100816', 'abnormal blastocoel anlage', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630218, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0141777', 'abnormal catabolic process', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(630219, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0131667', 'abnormal actin cytoskeleton', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(630220, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100852', 'abnormal interdigital region', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(630221, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0141266', 'abnormal surface breathing', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(630222, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100511', 'abnormal stylopod', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(630223, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0131677', 'abnormal actin filament', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(630224, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100416', 'abnormal ligament', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(630225, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0101451', 'abnormal dorsal lymph space', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(630226, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0101231', 'abnormal taste bud', 0.5, 6.642668884102504, 1.8224528641507445, 'HP:0410008', 'Abnormality of the peripheral nervous system'),
(630227, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0101569', 'abnormal activin-induced ectoderm', 0.5294117647058824, 1.706362323152461, 0.9504568842024205, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630228, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100337', 'abnormal zygote', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(630229, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100523', 'abnormal midgut', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(630230, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100135', 'abnormal surface structure', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630231, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100175', 'abnormal migrating neuroblast', 0.5416666666666666, 3.94131651835137, 1.46112278086876, 'UPHENO:0004523', 'abnormal nervous system'),
(630232, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0101405', 'abnormal ring structure', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(630233, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0126486', 'abnormally localised sensory system', 0.43333333333333335, 3.94131651835137, 1.3068679445984308, 'UPHENO:0004523', 'abnormal nervous system'),
(630234, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100627', 'abnormal pharyngeal region', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(630235, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100742', 'abnormal musculoskeletal system', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630236, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100800', 'abnormal ventral marginal zone', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630237, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0101497', 'abnormal ciliary axoneme', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(630238, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0141600', 'absent metamorphosis', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(630239, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100423', 'abnormal process', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630240, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0101463', 'abnormal right-ventral blastomere', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(630241, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100640', 'abnormal notochordal sheath', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(630242, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0125007', 'absent anatomical line', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630243, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100258', 'abnormal organ part', 0.5294117647058824, 1.706362323152461, 0.9504568842024205, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630244, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100394', 'abnormal marginal zone', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630245, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100427', 'abnormal olfactory system', 0.5909090909090909, 3.94131651835137, 1.526092972542627, 'UPHENO:0004523', 'abnormal nervous system'),
(630246, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100858', 'abnormal presumptive midbrain-hindbrain boundary', 0.5416666666666666, 3.94131651835137, 1.46112278086876, 'UPHENO:0004523', 'abnormal nervous system'),
(630247, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0107339', 'abnormal yolk platelet', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(630248, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100069', 'abnormal urinary system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(630249, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100393', 'abnormal involuting marginal zone', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630250, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100309', 'abnormal vegetal hemisphere', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630251, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100773', 'abnormal profundus ganglion', 0.5384615384615384, 6.642668884102504, 1.8912487162783285, 'HP:0410008', 'Abnormality of the peripheral nervous system'),
(630252, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0107286', 'abnormal efferent neuron', 0.5, 3.94131651835137, 1.4038013602984167, 'UPHENO:0004523', 'abnormal nervous system'),
(630253, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0126949', 'abnormally localised gustatory system', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(630254, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100974', 'abnormal cardiac mesoderm', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630255, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0101109', 'abnormal egg cell-free extract', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630256, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100907', 'abnormal cytoplasm', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(630257, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100649', 'abnormal growth cone', 0.48148148148148145, 3.94131651835137, 1.3775597686645948, 'UPHENO:0004523', 'abnormal nervous system'),
(630258, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100842', 'abnormal left-dorsal blastomere', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(630259, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0141892', 'abnormal inositol metabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(630260, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0126407', 'abnormally localised neuron', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(630261, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100398', 'abnormal vegetal blastomere', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(630262, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0101373', 'abnormal oxygen accumulating cell', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(630263, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0101368', 'abnormal regenerating eye', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630264, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100834', 'abnormal ventral lateral line', 0.5, 6.642668884102504, 1.8224528641507445, 'HP:0410008', 'Abnormality of the peripheral nervous system'),
(630265, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100261', 'abnormal multilaminar epithelium', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630266, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100225', 'abnormal endocrine system', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(630267, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0101083', 'abnormal T cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(630268, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0126887', 'abnormally localised nervous system', 0.4482758620689655, 3.94131651835137, 1.3292091859262085, 'UPHENO:0004523', 'abnormal nervous system'),
(630269, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100581', 'abnormal immune system', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(630270, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0107326', 'abnormal regenerating pelvic girdle', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630271, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100176', 'abnormal stage VI oocyte', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(630272, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100207', 'abnormal blastema', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630273, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0101513', 'abnormal basal body', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(630274, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100444', 'abnormal cement gland', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630275, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0116434', 'abnormal biological process', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(630276, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100164', 'abnormal neural nucleus', 0.5652173913043478, 3.94131651835137, 1.4925483713458991, 'UPHENO:0004523', 'abnormal nervous system'),
(630277, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0101133', 'abnormal motor neuron', 0.52, 3.94131651835137, 1.4316021058739445, 'UPHENO:0004523', 'abnormal nervous system'),
(630278, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100817', 'abnormal intersomitic neuron', 0.48148148148148145, 3.94131651835137, 1.3775597686645948, 'UPHENO:0004523', 'abnormal nervous system'),
(630279, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0101566', 'abnormal posterior lateral line', 0.5, 6.642668884102504, 1.8224528641507445, 'HP:0410008', 'Abnormality of the peripheral nervous system'),
(630280, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0101326', 'abnormal cementoblast', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(630281, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100146', 'abnormal primary germ layer', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630282, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0107271', 'abnormal apical region', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630283, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100232', 'abnormal lymphatic system', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(630284, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100638', 'abnormal polar body', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(630285, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100887', 'abnormal right-dorsal blastomere', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(630286, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100547', 'abnormal blastomere V2', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(630287, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100187', 'abnormal regenerating limb', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630288, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100687', 'abnormal periotic region', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(630289, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0126580', 'abnormally localised neural nucleus', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(630290, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0115758', 'abnormally decreased mobility of melanoblast', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(630291, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100433', 'abnormal pectoral appendage', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630292, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100265', 'abnormal sensory epithelial cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(630293, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0101283', 'abnormal left-ventral blastomere', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(630294, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0101570', 'abnormal forelimb region', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630295, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0115473', 'abnormally delayed phase of Mullerian duct', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(630296, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0141272', 'absent surface breathing', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(630297, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100032', 'abnormal nervous system', 0.65, 3.94131651835137, 1.6005798127329953, 'UPHENO:0004523', 'abnormal nervous system'),
(630298, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0141770', 'abnormal urate homeostasis', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(630299, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0127277', 'abnormally localised migrating neuroblast', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(630300, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100888', 'abnormal microtubule', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(630301, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0101149', 'abnormal amputated limb', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630302, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0141276', 'decreased surface breathing', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(630303, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0126318', 'abnormally localised cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(630304, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0101389', 'abnormal wedge region', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(630305, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100867', 'abnormal apical mesenchyme', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630306, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100791', 'abnormal multiciliated cell precursor', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(630307, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100103', 'abnormal trunk', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630308, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0127128', 'abnormally localised central nervous system', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(630309, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0101023', 'abnormal ultimobranchial body', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(630310, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0101263', 'abnormal blastocoel floor', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630311, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100458', 'abnormal autopod', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(630312, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100335', 'abnormal commissural interneuron', 0.48148148148148145, 3.94131651835137, 1.3775597686645948, 'UPHENO:0004523', 'abnormal nervous system'),
(630313, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100133', 'abnormal solid compound organ', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630314, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0107311', 'abnormal apical junction complex', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(630315, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100026', 'abnormal germ cell', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(630316, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0101098', 'abnormal mineralized extracellular matrix', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630317, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100002', 'abnormal head', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(630318, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100864', 'abnormal dorsolateral ascending neuron', 0.52, 3.94131651835137, 1.4316021058739445, 'UPHENO:0004523', 'abnormal nervous system'),
(630319, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0126397', 'abnormally localised glial cell', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(630320, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100203', 'abnormal endocrine cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(630321, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0101029', 'abnormal right spleen primordium', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(630322, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100378', 'abnormal perichondrium', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(630323, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100531', 'abnormal proliferative region', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630324, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100642', 'abnormal gustatory system', 0.5909090909090909, 3.94131651835137, 1.526092972542627, 'UPHENO:0004523', 'abnormal nervous system'),
(630325, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0131669', 'abnormal Roux spot', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(630326, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100093', 'abnormal simple squamous epithelium', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630327, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0101575', 'abnormal vitelline membrane', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(630328, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100477', 'abnormal pericyte', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(630329, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0101535', 'abnormal absorptive cell', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(630330, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0107272', 'abnormal axial region', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630331, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100363', 'abnormal cardiovascular system', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630332, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0101302', 'abnormal subcortical cytoplasm', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(630333, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100162', 'abnormal presumptive rhombomere', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630334, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100158', 'abnormal neuromere', 0.5416666666666666, 3.94131651835137, 1.46112278086876, 'UPHENO:0004523', 'abnormal nervous system'),
(630335, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0101450', 'abnormal myeloid cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(630336, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100913', 'abnormal Brachets cleft', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630337, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0101240', 'abnormal ciliated non-epidermal cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(630338, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100674', 'abnormal secondary oogonium', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(630339, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100445', 'abnormal spinal ganglion', 0.5384615384615384, 6.642668884102504, 1.8912487162783285, 'HP:0410008', 'Abnormality of the peripheral nervous system'),
(630340, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0141781', 'abnormal secondary metabolic process', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(630341, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100807', 'abnormal matrix-based tissue', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630342, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0101333', 'abnormal barrier epithelial cell', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(630343, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100296', 'abnormal tail region', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630344, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100201', 'abnormal cavitated compound organ', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630345, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0101396', 'abnormal apical epithelial cap', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630346, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100956', 'abnormal centrosome', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(630347, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100686', 'abnormal olfactory organ', 0.48148148148148145, 3.94131651835137, 1.3775597686645948, 'UPHENO:0004523', 'abnormal nervous system'),
(630348, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0101363', 'abnormal infraorbital lateral line', 0.5, 6.642668884102504, 1.8224528641507445, 'HP:0410008', 'Abnormality of the peripheral nervous system'),
(630349, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0101512', 'abnormal lateral funiculus', 0.4642857142857143, 3.94131651835137, 1.3527368387638634, 'UPHENO:0004523', 'abnormal nervous system'),
(630350, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100557', 'abnormal prime meridian', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630351, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0141743', 'abnormal chemical homeostasis within a tissue', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(630352, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100509', 'abnormal germ plasm', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(630353, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0101038', 'abnormal hyomandibular lateral line', 0.5, 6.642668884102504, 1.8224528641507445, 'HP:0410008', 'Abnormality of the peripheral nervous system'),
(630354, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100247', 'abnormal cranial ganglion', 0.42424242424242425, 6.642668884102504, 1.678720331333175, 'HP:0410008', 'Abnormality of the peripheral nervous system'),
(630355, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100060', 'abnormal regenerating tissue', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630356, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0131685', 'abnormal cortical actin cytoskeleton', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(630357, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0141267', 'abnormal resting posture', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(630358, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0101490', 'abnormal ectodermal cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(630359, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0141498', 'abnormal axon microtubule bundle', 0.4642857142857143, 3.94131651835137, 1.3527368387638634, 'UPHENO:0004523', 'abnormal nervous system'),
(630360, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0101269', 'abnormal mesodermal cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(630361, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100267', 'abnormal wound epidermis', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630362, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0107262', 'abnormal left-right axis', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630363, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100104', 'abnormal embryonic structure', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630364, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0101518', 'abnormal B cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(630365, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100546', 'abnormal whole organism', 0.5294117647058824, 1.706362323152461, 0.9504568842024205, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630366, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100999', 'abnormal serous membrane', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630367, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0131687', 'abnormal astral microtubule', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(630368, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100701', 'abnormal microglial cell', 0.52, 3.94131651835137, 1.4316021058739445, 'UPHENO:0004523', 'abnormal nervous system'),
(630369, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0101713', 'abnormal anatomical entity in vitro morphology', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630370, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0131730', 'abnormal regulation of protein folding', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(630371, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100610', 'abnormal appendage', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630372, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100014', 'abnormal tissue', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630373, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100268', 'abnormal circulatory system', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630374, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100170', 'abnormal anterior neural tube', 0.4642857142857143, 3.94131651835137, 1.3527368387638634, 'UPHENO:0004523', 'abnormal nervous system'),
(630375, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0101200', 'abnormal joint region', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630376, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100616', 'abnormal ventral blood island', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(630377, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0101270', 'abnormal caudal lateral line', 0.5, 6.642668884102504, 1.8224528641507445, 'HP:0410008', 'Abnormality of the peripheral nervous system'),
(630378, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0127918', 'abnormally localised principal cavity', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(630379, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100545', 'abnormal male organism', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630380, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100136', 'abnormal neural tube', 0.48148148148148145, 3.94131651835137, 1.3775597686645948, 'UPHENO:0004523', 'abnormal nervous system'),
(630381, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100328', 'abnormal supraorbital lateral line', 0.5, 6.642668884102504, 1.8224528641507445, 'HP:0410008', 'Abnormality of the peripheral nervous system'),
(630382, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0101409', 'abnormal perivitelline space', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(630383, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100846', 'abnormal hindlimb', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(630384, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100702', 'abnormal glial cell', 0.5416666666666666, 3.94131651835137, 1.46112278086876, 'UPHENO:0004523', 'abnormal nervous system'),
(630385, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0101424', 'abnormal coelomic epithelium', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630386, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100056', 'abnormal olfactory epithelium', 0.5, 3.94131651835137, 1.4038013602984167, 'UPHENO:0004523', 'abnormal nervous system'),
(630387, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100704', 'abnormal Merkel cell', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(630388, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0101402', 'abnormal oropharyngeal papilla', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(630389, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100255', 'abnormal pelvic appendage', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630390, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100151', 'abnormal primordium', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630391, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100372', 'abnormal hematological system', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(630392, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100417', 'abnormal dense regular connective tissue', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(630393, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0141778', 'abnormal biosynthetic process', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(630394, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0101224', 'abnormal dorsal involuting marginal zone', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630395, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0141860', 'abnormal malate-aspartate shuttle', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(630396, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0101260', 'abnormal central canal', 0.4642857142857143, 3.94131651835137, 1.3527368387638634, 'UPHENO:0004523', 'abnormal nervous system'),
(630397, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0115512', 'abnormally semi-erect whole organism', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630398, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100196', 'abnormal neuron', 0.5416666666666666, 3.94131651835137, 1.46112278086876, 'UPHENO:0004523', 'abnormal nervous system'),
(630399, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100667', 'abnormal vegetal yolk mass', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630400, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100114', 'abnormal peripheral nervous system', 0.6363636363636364, 6.642668884102504, 2.056004116301095, 'HP:0410008', 'Abnormality of the peripheral nervous system'),
(630401, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0101212', 'abnormal glomeral mesenchyme', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(630402, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0101035', 'abnormal ventrolateral neural tube', 0.4642857142857143, 3.94131651835137, 1.3527368387638634, 'UPHENO:0004523', 'abnormal nervous system'),
(630403, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0101553', 'abnormal dental epithelium', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630404, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0115391', 'abnormally undifferentiated alimentary system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(630405, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100860', 'abnormal parathyroid', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(630406, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0101160', 'abnormal ventral funiculus', 0.4642857142857143, 3.94131651835137, 1.3527368387638634, 'UPHENO:0004523', 'abnormal nervous system'),
(630407, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0107340', 'abnormal enteric nervous system morphology', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(630408, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0115574', 'abnormal variability of size of hindlimb', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(630409, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0101204', 'abnormal peripheral nerve', 0.4117647058823529, 6.642668884102504, 1.653849025557147, 'HP:0410008', 'Abnormality of the peripheral nervous system'),
(630410, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100415', 'abnormal secretory epithelial cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(630411, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0141271', 'increased surface breathing', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(630412, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100515', 'abnormal somatic stem cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(630413, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0107287', 'abnormal afferent neuron', 0.5, 3.94131651835137, 1.4038013602984167, 'UPHENO:0004523', 'abnormal nervous system'),
(630414, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100551', 'abnormal oocyte cortex', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(630415, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100481', 'abnormal anatomical line', 0.5625, 1.706362323152461, 0.9797085315405084, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630416, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100289', 'abnormal chondroblast', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(630417, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100231', 'abnormal compound organ', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630418, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100549', 'abnormal mitotic cell', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(630419, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100503', 'abnormal blastomere D2', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(630420, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0115630', 'abnormally delayed closure of neural tube', 0.4642857142857143, 3.94131651835137, 1.3527368387638634, 'UPHENO:0004523', 'abnormal nervous system'),
(630421, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0101334', 'abnormal olfactory pit', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(630422, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0101589', 'abnormal blastocoel roof', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630423, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0126772', 'abnormally localised lateral line system', 0.4117647058823529, 6.642668884102504, 1.653849025557147, 'HP:0410008', 'Abnormality of the peripheral nervous system'),
(630424, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0141904', 'abnormal glucosamine metabolic process', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(630425, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100437', 'abnormal proepicardium', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(630426, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100787', 'abnormal posterior neural tube', 0.4642857142857143, 3.94131651835137, 1.3527368387638634, 'UPHENO:0004523', 'abnormal nervous system'),
(630427, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0141718', 'abnormal posterior notochord', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(630428, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100851', 'abnormal infraorbital lateral line primordium', 0.4827586206896552, 6.642668884102504, 1.7907556137528693, 'HP:0410008', 'Abnormality of the peripheral nervous system'),
(630429, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100239', 'abnormal acellular anatomical structure', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630430, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100486', 'abnormal oral evagination', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(630431, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100025', 'abnormal oocyte', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(630432, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100006', 'abnormal anatomical structure', 0.5625, 1.706362323152461, 0.9797085315405084, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630433, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0101264', 'abnormal mitotic spindle', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(630434, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0101345', 'abnormal ascending interneuron', 0.48148148148148145, 3.94131651835137, 1.3775597686645948, 'UPHENO:0004523', 'abnormal nervous system'),
(630435, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100465', 'abnormal skeletal system', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(630436, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100010', 'abnormal multicellular anatomical structure', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630437, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100392', 'abnormal cilium', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(630438, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0107288', 'abnormal larval alimentary system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(630439, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100004', 'abnormal cell', 0.55, 1.8210412618256888, 1.0007860380741376, 'HP:0000118', 'Phenotypic abnormality'),
(630440, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100899', 'abnormal secondary spermatogonium', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(630441, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0101740', 'abnormal cell part morphology', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(630442, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0131723', 'abnormal pathway-restricted SMAD protein phosphorylation', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(630443, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0101237', 'abnormal mucus secreting cell', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(630444, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0141791', 'abnormal primary metabolic process', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(630445, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0141809', 'abnormal catalytic activity', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(630446, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100843', 'abnormal fasciculated network of fibrils', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(630447, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100915', 'abnormal dermal system', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630448, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100152', 'abnormal alimentary system', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(630449, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100031', 'abnormal central nervous system', 0.6190476190476191, 3.94131651835137, 1.5620059560060797, 'UPHENO:0004523', 'abnormal nervous system'),
(630450, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100985', 'abnormal simple columnar epithelium', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630451, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100070', 'abnormal anatomical system', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630452, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100856', 'abnormal simple organ', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630453, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100403', 'abnormal forelimb', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(630454, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0141783', 'abnormal collagen metabolic process', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(630455, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0141798', 'abnormal lipid metabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(630456, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0126409', 'abnormally localised enteric nervous system', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(630457, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100750', 'abnormal regenerating fin', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630458, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0126624', 'abnormally localised anatomical line', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630459, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0141772', 'abnormal water homeostasis', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(630460, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:00000000', 'Xenopus phenotype', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(630461, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100282', 'abnormal pelvic girdle primordium', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630462, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100501', 'abnormal urogenital system', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(630463, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100724', 'abnormal kinetochore', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(630464, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100521', 'abnormal animal blastomere', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(630465, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100108', 'abnormal cell part', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(630466, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0107312', 'abnormal filopodium', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(630467, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0102113', 'abnormal anatomical line morphology', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630468, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100377', 'abnormal connective tissue', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(630469, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100422', 'abnormal notochord', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(630470, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0115508', 'abnormally peramorphic growth of whole organism', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630471, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0141790', 'abnormal cellular metabolic process', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(630472, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100009', 'abnormal multi-tissue structure', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630473, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100954', 'abnormal neural progenitor cell', 0.52, 3.94131651835137, 1.4316021058739445, 'UPHENO:0004523', 'abnormal nervous system'),
(630474, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0101411', 'abnormal marginal zone (sensu neural)', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630475, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100721', 'abnormal centromere', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(630476, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0101174', 'abnormal articular system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(630477, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0141625', 'metaplastic spinal cord', 0.43333333333333335, 3.94131651835137, 1.3068679445984308, 'UPHENO:0004523', 'abnormal nervous system'),
(630478, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100081', 'abnormal anatomical entity in vitro', 0.5625, 1.706362323152461, 0.9797085315405084, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630479, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0101485', 'abnormal descending interneuron', 0.48148148148148145, 3.94131651835137, 1.3775597686645948, 'UPHENO:0004523', 'abnormal nervous system'),
(630480, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0141264', 'abnormal schooling behavior', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(630481, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0101560', 'abnormal compound organ component', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630482, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100727', 'abnormal odontogenic papilla', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(630483, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100172', 'abnormal stem cell', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(630484, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0101349', 'abnormal trunk region', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630485, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100274', 'abnormal sensory system', 0.6190476190476191, 3.94131651835137, 1.5620059560060797, 'UPHENO:0004523', 'abnormal nervous system'),
(630486, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0101906', 'abnormal sensory system morphology', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(630487, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0101297', 'abnormal barrier cell', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(630488, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100062', 'abnormal anatomical space', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630489, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100295', 'abnormal extracellular matrix', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630490, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100734', 'abnormal lateral line system', 0.5833333333333334, 6.642668884102504, 1.9684740746052836, 'HP:0410008', 'Abnormality of the peripheral nervous system'),
(630491, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0107276', 'abnormal dorsal region', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630492, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0101073', 'abnormal Bowmans gland', 0.4642857142857143, 3.94131651835137, 1.3527368387638634, 'UPHENO:0004523', 'abnormal nervous system'),
(630493, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0101472', 'abnormal zygote cortex', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(630494, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0107258', 'abnormal anatomical axis', 0.5294117647058824, 1.706362323152461, 0.9504568842024205, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630495, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0101366', 'abnormal morula cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(630496, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100320', 'abnormal lateral line', 0.5185185185185185, 6.642668884102504, 1.8558951556577463, 'HP:0410008', 'Abnormality of the peripheral nervous system'),
(630497, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0141715', 'abnormal septum', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630498, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0101543', 'abnormal external gill', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(630499, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0131691', 'abnormal molecular function', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(630500, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0101132', 'abnormal apoptotic cell', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(630501, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0126894', 'abnormally localised vestibuloauditory system', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(630502, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100694', 'abnormal lateral line primordium', 0.5, 6.642668884102504, 1.8224528641507445, 'HP:0410008', 'Abnormality of the peripheral nervous system'),
(630503, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100872', 'abnormal neuroendocrine cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(630504, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100386', 'abnormal limb', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(630505, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0141497', 'abnormal lymphoblast', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(630506, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0116091', 'abnormally increased variability of size of cell in endoderm', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(630507, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100574', 'abnormal gastrula cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(630508, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0141754', 'abnormal homeostatic process', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(630509, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0101099', 'abnormal ventro-lateral marginal zone', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630510, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0101040', 'abnormal axial mesoderm', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630511, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0131469', 'abnormal heart process', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(630512, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0101092', 'abnormal dorso-lateral marginal zone', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630513, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0127101', 'abnormally localised portion of organism substance', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630514, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100468', 'abnormal muscular system', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630515, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0101500', 'abnormal endodermal cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(630516, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100339', 'abnormal circumblastoporal collar', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630517, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100429', 'abnormal spermatid', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(630518, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100585', 'abnormal elastica externa', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(630519, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0107261', 'abnormal dorsal-ventral axis', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630520, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100599', 'abnormal adult immune system', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(630521, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0141795', 'abnormal glycosylation', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(630522, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0115362', 'abnormally decreased adhesivity of prechordal plate', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630523, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0101004', 'abnormal acid secreting cell', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(630524, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0101061', 'abnormal plasma membrane', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(630525, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0141748', 'abnormal gas homeostasis', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(630526, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0107267', 'abnormal ventral side', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630527, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100760', 'abnormal Stirnorgan', 0.52, 3.94131651835137, 1.4316021058739445, 'UPHENO:0004523', 'abnormal nervous system'),
(630528, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100317', 'abnormal respiratory system', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(630529, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100894', 'abnormal nucleus', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(630530, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100332', 'abnormal germinal granule', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(630531, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0125261', 'absent nervous system', 0.43333333333333335, 3.94131651835137, 1.3068679445984308, 'UPHENO:0004523', 'abnormal nervous system'),
(630532, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0107260', 'abnormal anterior-posterior axis', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630533, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0126755', 'abnormally localised medium cavity', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(630534, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100273', 'abnormal visual system', 0.5909090909090909, 3.94131651835137, 1.526092972542627, 'UPHENO:0004523', 'abnormal nervous system'),
(630535, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0141745', 'abnormal creatinine homeostasis', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(630536, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0115505', 'dead whole organism', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630537, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0101115', 'abnormal trunk lateral line', 0.5, 6.642668884102504, 1.8224528641507445, 'HP:0410008', 'Abnormality of the peripheral nervous system'),
(630538, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0141794', 'abnormal prosthetic group metabolic process', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(630539, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100277', 'abnormal blastocoel', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630540, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100900', 'abnormal angioblast', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(630541, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0141263', 'abnormal visually guided collision avoidance behavior', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(630542, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100336', 'abnormal interneuron', 0.5, 3.94131651835137, 1.4038013602984167, 'UPHENO:0004523', 'abnormal nervous system'),
(630543, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0101162', 'abnormal stromal cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(630544, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100383', 'abnormal amputated fin', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630545, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100691', 'abnormal keratin accumulating cell', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(630546, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0107263', 'abnormal anatomical side', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630547, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100605', 'abnormal prechordal plate', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630548, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0141775', 'abnormal nitrogen compound metabolic process', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(630549, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0101362', 'abnormal vegetal cortex', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(630550, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0141499', 'abnormal tadpole', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630551, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0101503', 'abnormal organ cortex', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630552, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0107264', 'abnormal anterior side', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630553, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100891', 'abnormal dorsal lateral line', 0.5, 6.642668884102504, 1.8224528641507445, 'HP:0410008', 'Abnormality of the peripheral nervous system'),
(630554, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100665', 'abnormal egg jelly', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630555, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100762', 'abnormal intersomitic region', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630556, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100084', 'abnormal anatomical group', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630557, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0142054', 'abnormal digestive tract', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(630558, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100715', 'abnormal ciliated cell', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(630559, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0101176', 'abnormal non-ciliated epithelial cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(630560, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0141714', 'abnormal anterior notochord', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(630561, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0107269', 'abnormal right side', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630562, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100623', 'abnormal olfactory sensory neuron', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(630563, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100735', 'abnormal hindgut', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(630564, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0141841', 'abnormality of whole organism mass', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(630565, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0126501', 'abnormally localised visual system', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(630566, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100449', 'abnormal lymphocyte', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(630567, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100384', 'abnormal amputated tissue', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630568, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100688', 'abnormal adipose tissue', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(630569, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100786', 'abnormal presumptive axial mesoderm', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630570, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0131675', 'abnormal spindle microtubule', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(630571, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100781', 'abnormal presumptive ectoderm', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630572, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0101347', 'abnormal hindlimb region', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630573, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0101435', 'abnormal paracrine cell', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(630574, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0124877', 'absent sensory system', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(630575, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0101519', 'abnormal hypobranchial placode', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630576, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0107273', 'abnormal basal region', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630577, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0101072', 'abnormal mitochondrial cloud', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(630578, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0101547', 'abnormal lampbrush chromosome', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(630579, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0107253', 'abnormal enteric nervous system', 0.6190476190476191, 3.94131651835137, 1.5620059560060797, 'UPHENO:0004523', 'abnormal nervous system'),
(630580, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0116494', 'absent biological process', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(630581, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0141265', 'abnormal escape behavior', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(630582, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100003', 'abnormal organism subdivision', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630583, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0101136', 'abnormal ooplasm', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(630584, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100862', 'abnormal blastomere V1', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(630585, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100754', 'abnormal electrically active cell', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(630586, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100156', 'abnormal foregut', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(630587, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100242', 'abnormal right lymph heart', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(630588, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100588', 'abnormal unicellular gland', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630589, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100307', 'abnormal blastomere', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(630590, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100228', 'abnormal skeletal subdivision', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(630591, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100995', 'abnormal otic vesicle', 0.4642857142857143, 3.94131651835137, 1.3527368387638634, 'UPHENO:0004523', 'abnormal nervous system'),
(630592, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0107257', 'abnormal peripheral ganglion', 0.5384615384615384, 6.642668884102504, 1.8912487162783285, 'HP:0410008', 'Abnormality of the peripheral nervous system'),
(630593, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100120', 'abnormal genital system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(630594, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100587', 'abnormal vestibuloauditory system', 0.5909090909090909, 3.94131651835137, 1.526092972542627, 'UPHENO:0004523', 'abnormal nervous system'),
(630595, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100612', 'abnormal unilaminar epithelium', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630596, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100976', 'abnormal multiciliated cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(630597, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100917', 'abnormal stage III oocyte', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(630598, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100991', 'abnormal iliac process primordium', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630599, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0142051', 'abnormal cerebrospinal fluid', 0.5652173913043478, 3.94131651835137, 1.4925483713458991, 'UPHENO:0004523', 'abnormal nervous system'),
(630600, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0124803', 'absent enteric nervous system', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(630601, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100202', 'abnormal embryo', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630602, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100358', 'abnormal ganglion', 0.56, 6.642668884102504, 1.9287028218721003, 'HP:0410008', 'Abnormality of the peripheral nervous system'),
(630603, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0142056', 'abnormal main body axis', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630604, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0127419', 'abnormally localised presumptive midbrain-hindbrain boundary', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(630605, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100912', 'abnormal trabecula', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630606, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0107278', 'abnormal medial region', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630607, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0101239', 'abnormal olfactory epithelial support cell', 0.5, 3.94131651835137, 1.4038013602984167, 'UPHENO:0004523', 'abnormal nervous system'),
(630608, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0141787', 'abnormal hormone metabolic process', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(630609, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0101638', 'abnormal anatomical structure morphology', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630610, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100626', 'abnormal primordial germ cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(630611, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100890', 'abnormal pharyngeal cavity', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(630612, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0101514', 'abnormal dendrite', 0.48148148148148145, 3.94131651835137, 1.3775597686645948, 'UPHENO:0004523', 'abnormal nervous system'),
(630613, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0101078', 'abnormal mucous gland', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630614, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100285', 'abnormal progenitor cell', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(630615, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100902', 'abnormal spermatocyte', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(630616, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0126426', 'abnormally localised peripheral nervous system', 0.4375, 6.642668884102504, 1.7047485552992399, 'HP:0410008', 'Abnormality of the peripheral nervous system'),
(630617, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100796', 'abnormal pseudoblastema', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630618, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0141619', 'metaplastic olfactory organ', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(630619, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0142024', 'abnormally localised cerebrospinal fluid', 0.43333333333333335, 3.94131651835137, 1.3068679445984308, 'UPHENO:0004523', 'abnormal nervous system'),
(630620, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100249', 'abnormal avascular GAG-rich matrix', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630621, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0101107', 'abnormal erythroid cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(630622, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0101468', 'abnormal stage I oocyte', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(630623, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0107285', 'abnormal flexural organ', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(630624, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100874', 'abnormal occipital lateral line', 0.5, 6.642668884102504, 1.8224528641507445, 'HP:0410008', 'Abnormality of the peripheral nervous system'),
(630625, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0101377', 'abnormal manicotto glandulare', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(630626, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100812', 'abnormal sulcus limitans of neural tube', 0.43333333333333335, 3.94131651835137, 1.3068679445984308, 'UPHENO:0004523', 'abnormal nervous system'),
(630627, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100802', 'abnormal exocrine cell', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(630628, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0101403', 'abnormal basal lamina', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630629, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100726', 'abnormal tail', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630630, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0101157', 'abnormal female organism', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630631, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0131666', 'abnormal adherens junction', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(630632, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100167', 'abnormal nerve', 0.4117647058823529, 6.642668884102504, 1.653849025557147, 'HP:0410008', 'Abnormality of the peripheral nervous system'),
(630633, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0131729', 'abnormal regulation of growth rate', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(630634, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100573', 'abnormal extraembryonic structure', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630635, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100799', 'abnormal genital ridge', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(630636, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100067', 'abnormal animal hemisphere', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630637, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0101312', 'abnormal trigeminal ganglion', 0.4117647058823529, 6.642668884102504, 1.653849025557147, 'HP:0410008', 'Abnormality of the peripheral nervous system'),
(630638, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100059', 'abnormal regenerating tail', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630639, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0141776', 'abnormal metabolic process', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(630640, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0101010', 'abnormal dorsal marginal zone', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630641, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100935', 'abnormal skeleton', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(630642, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100707', 'abnormal central vegetal yolk mass', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630643, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100344', 'abnormal portion of organism substance', 0.5625, 1.706362323152461, 0.9797085315405084, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630644, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0101241', 'abnormal nucleate erythrocyte', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(630645, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0101113', 'abnormal stage IV oocyte', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(630646, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100205', 'abnormal limb segment', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(630647, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100653', 'abnormal myoblast', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(630648, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0141797', 'abnormal hydrogen metabolic process', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(630649, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100308', 'abnormal early embryonic cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(630650, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0101406', 'abnormal cleavage furrow', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630651, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0101587', 'abnormal hemangioblast', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(630652, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0101393', 'abnormal dorsolateral neural tube', 0.4642857142857143, 3.94131651835137, 1.3527368387638634, 'UPHENO:0004523', 'abnormal nervous system'),
(630653, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100827', 'abnormal atypical epithelium', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630654, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0141786', 'abnormal pigment metabolic process', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(630655, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100570', 'abnormal axon', 0.48148148148148145, 3.94131651835137, 1.3775597686645948, 'UPHENO:0004523', 'abnormal nervous system'),
(630656, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0141784', 'abnormal cellular hormone metabolic process', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(630657, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0131725', 'abnormal phosphorylation of RNA polymerase II C-terminal domain', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(630658, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0101501', 'abnormal parabrachial area', 0.5416666666666666, 3.94131651835137, 1.46112278086876, 'UPHENO:0004523', 'abnormal nervous system'),
(630659, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0133403', 'abnormal developmental process', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(630660, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0107268', 'abnormal left side', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630661, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100100', 'abnormal muscle', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(630662, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100741', 'abnormal blastopore', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630663, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100186', 'abnormal uveal tract', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630664, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0141907', 'abnormal putrescine metabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(630665, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0141738', 'abnormal carbon dioxide homeostasis', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(630666, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100023', 'abnormal mesenchyme', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630667, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0115566', 'abnormal variability of size of forelimb', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(630668, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100192', 'abnormal epithelium', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630669, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100728', 'abnormal cell condensation', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630670, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100916', 'abnormal principal cavity', 0.5416666666666666, 3.94131651835137, 1.46112278086876, 'UPHENO:0004523', 'abnormal nervous system'),
(630671, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100823', 'abnormal blood', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(630672, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0101533', 'abnormal simple cuboidal epithelium', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630673, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0101311', 'abnormal bottle cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(630674, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100664', 'abnormal periocular region', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(630675, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100784', 'abnormal left blastomere', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(630676, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100028', 'abnormal anatomical cluster', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630677, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0131745', 'abnormal axis elongation', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(630678, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0101310', 'abnormal pigment layer', 0.4642857142857143, 3.94131651835137, 1.3527368387638634, 'UPHENO:0004523', 'abnormal nervous system'),
(630679, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0101370', 'abnormal floor plate', 0.48148148148148145, 3.94131651835137, 1.3775597686645948, 'UPHENO:0004523', 'abnormal nervous system'),
(630680, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0101467', 'abnormal alkali secreting cell', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(630681, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0101573', 'abnormal peripheral vegetal yolk mass', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630682, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0101074', 'abnormal germinal vesicle', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(630683, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100482', 'abnormal Mullerian duct', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(630684, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100402', 'abnormal zeugopod', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(630685, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0141782', 'abnormal methylation', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(630686, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0131654', 'abnormal neuron projection', 0.5, 3.94131651835137, 1.4038013602984167, 'UPHENO:0004523', 'abnormal nervous system'),
(630687, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100376', 'abnormal animal pole', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630688, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100745', 'abnormal anterior lymph sac', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(630689, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0101460', 'abnormal fibrocellular pad', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630690, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100553', 'abnormal laryngeal muscle primordium', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630691, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0101448', 'abnormal myelin accumulating cell', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(630692, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100189', 'abnormal enteroendocrine cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(630693, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0128000', 'absent behavior', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(630694, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0133388', 'absent insulin receptor signaling pathway', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(630695, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0141315', 'abnormal anatomical region', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630696, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0124719', 'absent anatomical structure', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630697, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100569', 'abnormal motor axon', 0.4482758620689655, 3.94131651835137, 1.3292091859262085, 'UPHENO:0004523', 'abnormal nervous system'),
(630698, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100251', 'abnormal proteinaceous extracellular matrix', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630699, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0101096', 'abnormal tendon', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(630700, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0141796', 'abnormal demethylation', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(630701, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0107259', 'abnormal animal-vegetal axis', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630702, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100459', 'abnormal optic vesicle', 0.48148148148148145, 3.94131651835137, 1.3775597686645948, 'UPHENO:0004523', 'abnormal nervous system'),
(630703, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0101664', 'abnormal nervous system morphology', 0.43333333333333335, 3.94131651835137, 1.3068679445984308, 'UPHENO:0004523', 'abnormal nervous system'),
(630704, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0115509', 'abnormally semi-viable whole organism', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630705, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0101220', 'abnormal centriole', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(630706, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0101071', 'abnormal endoplasmic reticulum', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(630707, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100989', 'abnormal right blastomere', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(630708, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0101187', 'abnormal dorsolateral commissural neuron', 0.52, 3.94131651835137, 1.4316021058739445, 'UPHENO:0004523', 'abnormal nervous system'),
(630709, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0101168', 'abnormal circulating cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(630710, 'HP:0410008', 'Abnormality of the peripheral nervous system', 'XPO:0100854', 'abnormal spiracle', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630711, 'HP:0031443', 'Abnormal tricuspid valve leaflet morphology', 'XPO:0102510', 'abnormal right atrium morphology', 0.453125, 11.854497839006713, 2.3176646291687493, 'UPHENO:0019915', 'abnormal right cardiac atrium morphology'),
(630712, 'HP:0031443', 'Abnormal tricuspid valve leaflet morphology', 'XPO:0140009', 'abnormally necrotic right atrium', 0.4084507042253521, 11.854497839006713, 2.2004494973937048, 'UPHENO:0019915', 'abnormal right cardiac atrium morphology'),
(630713, 'HP:0031443', 'Abnormal tricuspid valve leaflet morphology', 'XPO:0141651', 'neoplastic right atrium', 0.43283582089552236, 11.854497839006713, 2.2651823995984666, 'UPHENO:0019915', 'abnormal right cardiac atrium morphology'),
(630714, 'HP:0031443', 'Abnormal tricuspid valve leaflet morphology', 'XPO:0102769', 'abnormal cardiac valve morphology', 0.41935483870967744, 10.21769640676594, 2.06998561073351, 'UPHENO:0015319', 'abnormal cardiac valve morphology in the heart'),
(630715, 'HP:0000852', 'Pseudohypoparathyroidism', 'XPO:0100225', 'abnormal endocrine system', 0.4482758620689655, 6.2194654996189955, 1.669741374719419, 'UPHENO:0003116', 'abnormal endocrine system'),
(630716, 'HP:0000852', 'Pseudohypoparathyroidism', 'XPO:0100860', 'abnormal parathyroid', 0.46875, 12.404694921567193, 2.4113690601989197, 'HP:0000828', 'Abnormality of the parathyroid gland'),
(630717, 'HP:0000852', 'Pseudohypoparathyroidism', 'XPO:0101023', 'abnormal ultimobranchial body', 0.40625, 6.2194654996189955, 1.5895464319170476, 'UPHENO:0003116', 'abnormal endocrine system'),
(630718, 'HP:0006499', 'Abnormal femoral epiphysis morphology', 'XPO:0103008', 'abnormal iliac process morphology', 0.4044943820224719, 7.61213700143767, 1.7547269452159566, 'UPHENO:0079871', 'abnormal anatomical entity morphology in the skeleton of pelvic complex'),
(630719, 'HP:0006499', 'Abnormal femoral epiphysis morphology', 'XPO:0141562', 'abnormal femur morphology in the regenerating hindlimb', 0.40540540540540543, 10.819732420846037, 2.094368164495225, 'HP:0002823', 'Abnormal femur morphology'),
(630720, 'HP:0006499', 'Abnormal femoral epiphysis morphology', 'XPO:0102033', 'abnormal femur morphology', 0.42452830188679247, 10.819732420846037, 2.143194492222123, 'HP:0002823', 'Abnormal femur morphology'),
(630721, 'HP:0006499', 'Abnormal femoral epiphysis morphology', 'XPO:0141567', 'abnormal joint region morphology in the femur', 0.422680412371134, 10.627087342903641, 2.1194012504484774, 'UPHENO:0087558', 'abnormal femur morphology'),
(630722, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0125160', 'absent exocrine cell', 0.42424242424242425, 3.6715585125471644, 1.2480508339450433, 'UPHENO:0086172', 'abnormal cell'),
(630723, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0140566', 'abnormally necrotic apical region', 0.41379310344827586, 2.7446671847279203, 1.0657036887902793, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(630724, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0131551', 'abnormally localised actin cytoskeleton', 0.4375, 3.6715585125471644, 1.2674016132384338, 'UPHENO:0086172', 'abnormal cell'),
(630725, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102228', 'abnormal myocyte morphology', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(630726, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0127743', 'abnormally localised perivitelline space', 0.42424242424242425, 3.6715585125471644, 1.2480508339450433, 'UPHENO:0086172', 'abnormal cell'),
(630727, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102669', 'abnormal hatching gland cell morphology', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(630728, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0100415', 'abnormal secretory epithelial cell', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(630729, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102752', 'abnormal cardiac progenitor cell morphology', 0.4186046511627907, 5.43643956286526, 1.5085486027240909, 'HP:0025461', 'Abnormal cell morphology'),
(630730, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0100574', 'abnormal gastrula cell', 0.5, 3.6715585125471644, 1.3549093166236559, 'UPHENO:0086172', 'abnormal cell'),
(630731, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0140098', 'abnormally necrotic secondary spermatogonium', 0.5142857142857142, 5.43643956286526, 1.6720894724144628, 'HP:0025461', 'Abnormal cell morphology'),
(630732, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0140393', 'abnormally necrotic spermatocyte', 0.5142857142857142, 5.43643956286526, 1.6720894724144628, 'HP:0025461', 'Abnormal cell morphology'),
(630733, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0127428', 'abnormally localised endoplasmic reticulum', 0.4375, 3.6715585125471644, 1.2674016132384338, 'UPHENO:0086172', 'abnormal cell'),
(630734, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0125750', 'absent melanoblast', 0.42424242424242425, 3.6715585125471644, 1.2480508339450433, 'UPHENO:0086172', 'abnormal cell'),
(630735, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102306', 'abnormal secondary oogonium morphology', 0.6, 5.43643956286526, 1.8060630492092893, 'HP:0025461', 'Abnormal cell morphology'),
(630736, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0101547', 'abnormal lampbrush chromosome', 0.52, 3.6715585125471644, 1.3817418089225373, 'UPHENO:0086172', 'abnormal cell'),
(630737, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0101485', 'abnormal descending interneuron', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(630738, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0140944', 'abnormally necrotic blastomere V1', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(630739, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0140082', 'abnormally necrotic interneuron', 0.4186046511627907, 5.43643956286526, 1.5085486027240909, 'HP:0025461', 'Abnormal cell morphology'),
(630740, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0103010', 'abnormal blastomere D1 morphology', 0.5294117647058824, 5.43643956286526, 1.696500828969256, 'HP:0025461', 'Abnormal cell morphology'),
(630741, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0131627', 'increased size of the actin cytoskeleton', 0.45714285714285713, 3.6715585125471644, 1.2955411026258445, 'UPHENO:0086172', 'abnormal cell'),
(630742, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0140450', 'abnormally necrotic mesenchymal stem cell', 0.5142857142857142, 5.43643956286526, 1.6720894724144628, 'HP:0025461', 'Abnormal cell morphology'),
(630743, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0100814', 'abnormal natural killer cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(630744, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0131597', 'decreased size of the spindle microtubule', 0.42105263157894735, 3.6715585125471644, 1.2433500608051093, 'UPHENO:0086172', 'abnormal cell'),
(630745, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0131328', 'abnormally decreased number of paracrine cell', 0.4117647058823529, 3.6715585125471644, 1.229560169755361, 'UPHENO:0086172', 'abnormal cell'),
(630746, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0129421', 'decreased size of the cementoblast', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(630747, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0128903', 'decreased size of the multiciliated cell', 0.4186046511627907, 5.43643956286526, 1.5085486027240909, 'HP:0025461', 'Abnormal cell morphology'),
(630748, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0140752', 'abnormally necrotic melanoblast', 0.5625, 5.43643956286526, 1.748713027947041, 'HP:0025461', 'Abnormal cell morphology'),
(630749, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102965', 'abnormal barrier epithelial cell morphology', 0.6428571428571429, 5.43643956286526, 1.869452862390249, 'HP:0025461', 'Abnormal cell morphology'),
(630750, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0103433', 'decreased size of the germ cell', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(630751, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102475', 'abnormal fasciculated network of fibrils morphology', 0.4444444444444444, 3.6715585125471644, 1.2774207542365574, 'UPHENO:0086172', 'abnormal cell'),
(630752, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0125779', 'absent endoplasmic reticulum', 0.42424242424242425, 3.6715585125471644, 1.2480508339450433, 'UPHENO:0086172', 'abnormal cell'),
(630753, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0101136', 'abnormal ooplasm', 0.48148148148148145, 3.6715585125471644, 1.3295816755533123, 'UPHENO:0086172', 'abnormal cell'),
(630754, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0101635', 'abnormal organism subdivision morphology', 0.42857142857142855, 2.7446671847279203, 1.0845671654222093, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(630755, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0133485', 'increased size of the cilium in ciliated non-epidermal cell', 0.41025641025641024, 3.6715585125471644, 1.2273061620492112, 'UPHENO:0086172', 'abnormal cell'),
(630756, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0125013', 'absent early embryonic cell', 0.4117647058823529, 3.6715585125471644, 1.229560169755361, 'UPHENO:0086172', 'abnormal cell'),
(630757, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0100546', 'abnormal whole organism', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630758, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0103099', 'abnormal alkali secreting cell morphology', 0.6428571428571429, 5.43643956286526, 1.869452862390249, 'HP:0025461', 'Abnormal cell morphology'),
(630759, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102819', 'abnormal dorsolateral commissural neuron morphology', 0.4864864864864865, 5.43643956286526, 1.626270082715184, 'HP:0025461', 'Abnormal cell morphology'),
(630760, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0131096', 'abnormally increased number of exocrine cell', 0.42424242424242425, 3.6715585125471644, 1.2480508339450433, 'UPHENO:0086172', 'abnormal cell'),
(630761, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0101808', 'abnormal stage VI oocyte morphology', 0.5625, 5.43643956286526, 1.748713027947041, 'HP:0025461', 'Abnormal cell morphology'),
(630762, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0101405', 'abnormal ring structure', 0.48148148148148145, 3.6715585125471644, 1.3295816755533123, 'UPHENO:0086172', 'abnormal cell'),
(630763, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0101740', 'abnormal cell part morphology', 0.5925925925925926, 3.6715585125471644, 1.4750384326537824, 'UPHENO:0086172', 'abnormal cell'),
(630764, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0128102', 'decreased size of the portion of organism substance', 0.4444444444444444, 2.7446671847279203, 1.104469140402437, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(630765, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0101804', 'abnormal stem cell morphology', 0.6428571428571429, 5.43643956286526, 1.869452862390249, 'HP:0025461', 'Abnormal cell morphology'),
(630766, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102790', 'abnormal blastomere V2.2.2 morphology', 0.43902439024390244, 5.43643956286526, 1.5449043867452603, 'HP:0025461', 'Abnormal cell morphology'),
(630767, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102824', 'abnormal blastomere D2.1 morphology', 0.43902439024390244, 5.43643956286526, 1.5449043867452603, 'HP:0025461', 'Abnormal cell morphology'),
(630768, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102586', 'abnormal neural progenitor cell morphology', 0.4864864864864865, 5.43643956286526, 1.626270082715184, 'HP:0025461', 'Abnormal cell morphology'),
(630769, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0128382', 'decreased size of the myoblast', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(630770, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0130037', 'increased size of the secondary oogonium', 0.4186046511627907, 5.43643956286526, 1.5085486027240909, 'HP:0025461', 'Abnormal cell morphology'),
(630771, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0131383', 'abnormally decreased number of cementoblast', 0.4117647058823529, 3.6715585125471644, 1.229560169755361, 'UPHENO:0086172', 'abnormal cell'),
(630772, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0140239', 'abnormally necrotic absorptive cell', 0.5625, 5.43643956286526, 1.748713027947041, 'HP:0025461', 'Abnormal cell morphology'),
(630773, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0115704', 'abnormally defasciculated motor neuron', 0.47368421052631576, 5.43643956286526, 1.6047291305419304, 'HP:0025461', 'Abnormal cell morphology'),
(630774, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0140269', 'abnormally necrotic anatomical line', 0.48, 2.7446671847279203, 1.1477979999413668, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(630775, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0141334', 'increased pigmentation in the whole organism', 0.42857142857142855, 2.7446671847279203, 1.0845671654222093, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(630776, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0131297', 'abnormally decreased number of melanoblast', 0.4117647058823529, 3.6715585125471644, 1.229560169755361, 'UPHENO:0086172', 'abnormal cell'),
(630777, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0100649', 'abnormal growth cone', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(630778, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0101107', 'abnormal erythroid cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(630779, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0101940', 'abnormal early embryonic cell morphology', 0.6, 5.43643956286526, 1.8060630492092893, 'HP:0025461', 'Abnormal cell morphology'),
(630780, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102178', 'abnormal whole organism morphology', 0.48, 2.7446671847279203, 1.1477979999413668, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(630781, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0127372', 'abnormally localised polar body', 0.45161290322580644, 3.6715585125471644, 1.2876813267322194, 'UPHENO:0086172', 'abnormal cell'),
(630782, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0100396', 'abnormal dorsal animal hemisphere blastomere', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(630783, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0125976', 'absent centriole', 0.4117647058823529, 3.6715585125471644, 1.229560169755361, 'UPHENO:0086172', 'abnormal cell'),
(630784, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0100437', 'abnormal proepicardium', 0.52, 3.6715585125471644, 1.3817418089225373, 'UPHENO:0086172', 'abnormal cell'),
(630785, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0100859', 'abnormal blastomere V1.1.2', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(630786, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0130483', 'increased size of the myelin accumulating cell', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(630787, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0107287', 'abnormal afferent neuron', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(630788, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102539', 'abnormal cytoplasm morphology', 0.5517241379310345, 3.6715585125471644, 1.423266473714053, 'UPHENO:0086172', 'abnormal cell'),
(630789, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0142067', 'abnormally necrotic desmosome', 0.5, 3.6715585125471644, 1.3549093166236559, 'UPHENO:0086172', 'abnormal cell'),
(630790, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102711', 'abnormal blastomere D1.1.2 morphology', 0.43902439024390244, 5.43643956286526, 1.5449043867452603, 'HP:0025461', 'Abnormal cell morphology'),
(630791, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0101917', 'abnormal progenitor cell morphology', 0.6428571428571429, 5.43643956286526, 1.869452862390249, 'HP:0025461', 'Abnormal cell morphology'),
(630792, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0130968', 'abnormally increased number of early embryonic cell', 0.4117647058823529, 3.6715585125471644, 1.229560169755361, 'UPHENO:0086172', 'abnormal cell'),
(630793, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0101350', 'abnormal blastomere D2.1.2', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(630794, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0103112', 'abnormal stage V oocyte morphology', 0.5625, 5.43643956286526, 1.748713027947041, 'HP:0025461', 'Abnormal cell morphology'),
(630795, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0101241', 'abnormal nucleate erythrocyte', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(630796, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102549', 'abnormal stage III oocyte morphology', 0.5625, 5.43643956286526, 1.748713027947041, 'HP:0025461', 'Abnormal cell morphology'),
(630797, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0131591', 'decreased size of the Roux spot', 0.43243243243243246, 3.6715585125471644, 1.2600400701560144, 'UPHENO:0086172', 'abnormal cell'),
(630798, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0100852', 'abnormal interdigital region', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(630799, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0130215', 'increased size of the perivitelline space', 0.43243243243243246, 3.6715585125471644, 1.2600400701560144, 'UPHENO:0086172', 'abnormal cell'),
(630800, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0100196', 'abnormal neuron', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(630801, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0140144', 'abnormally necrotic portion of organism substance', 0.48, 2.7446671847279203, 1.1477979999413668, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(630802, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0101158', 'abnormal blastomere V2.2.2', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(630803, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0141286', 'abnormal neuron projection morphology', 0.43243243243243246, 3.6715585125471644, 1.2600400701560144, 'UPHENO:0086172', 'abnormal cell'),
(630804, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0101497', 'abnormal ciliary axoneme', 0.48148148148148145, 3.6715585125471644, 1.3295816755533123, 'UPHENO:0086172', 'abnormal cell'),
(630805, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0131559', 'abnormally localised spindle microtubule', 0.4117647058823529, 3.6715585125471644, 1.229560169755361, 'UPHENO:0086172', 'abnormal cell'),
(630806, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0125530', 'absent chondroblast', 0.42424242424242425, 3.6715585125471644, 1.2480508339450433, 'UPHENO:0086172', 'abnormal cell'),
(630807, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0128156', 'decreased size of the chondroblast', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(630808, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102334', 'abnormal glial cell morphology', 0.5142857142857142, 5.43643956286526, 1.6720894724144628, 'HP:0025461', 'Abnormal cell morphology'),
(630809, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0131292', 'abnormally decreased number of mucus secreting cell', 0.4117647058823529, 3.6715585125471644, 1.229560169755361, 'UPHENO:0086172', 'abnormal cell'),
(630810, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0103636', 'abnormally increased number of melanoblast', 0.42424242424242425, 3.6715585125471644, 1.2480508339450433, 'UPHENO:0086172', 'abnormal cell'),
(630811, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0140169', 'abnormally necrotic stage VI oocyte', 0.47368421052631576, 5.43643956286526, 1.6047291305419304, 'HP:0025461', 'Abnormal cell morphology'),
(630812, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0100225', 'abnormal endocrine system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(630813, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0129365', 'decreased size of the absorptive cell', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(630814, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0140647', 'abnormally necrotic nucleate erythrocyte', 0.5625, 5.43643956286526, 1.748713027947041, 'HP:0025461', 'Abnormal cell morphology'),
(630815, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0140123', 'abnormally necrotic perichondrial cell', 0.4186046511627907, 5.43643956286526, 1.5085486027240909, 'HP:0025461', 'Abnormal cell morphology'),
(630816, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0141285', 'abnormal cortical actin cytoskeleton morphology', 0.5333333333333333, 3.6715585125471644, 1.399344325041251, 'UPHENO:0086172', 'abnormal cell'),
(630817, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0101964', 'abnormal germinal granule morphology', 0.45714285714285713, 3.6715585125471644, 1.2955411026258445, 'UPHENO:0086172', 'abnormal cell'),
(630818, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0100285', 'abnormal progenitor cell', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(630819, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0140899', 'abnormally necrotic mucus secreting cell', 0.5625, 5.43643956286526, 1.748713027947041, 'HP:0025461', 'Abnormal cell morphology'),
(630820, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0101969', 'abnormal zygote morphology', 0.6428571428571429, 5.43643956286526, 1.869452862390249, 'HP:0025461', 'Abnormal cell morphology'),
(630821, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0101162', 'abnormal stromal cell', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(630822, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0140096', 'abnormally necrotic gastrula cell', 0.4864864864864865, 5.43643956286526, 1.626270082715184, 'HP:0025461', 'Abnormal cell morphology'),
(630823, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0101890', 'abnormal organ part morphology', 0.48, 2.7446671847279203, 1.1477979999413668, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(630824, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0101967', 'abnormal commissural interneuron morphology', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(630825, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0107286', 'abnormal efferent neuron', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(630826, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0131131', 'abnormally increased number of absorptive cell', 0.42424242424242425, 3.6715585125471644, 1.2480508339450433, 'UPHENO:0086172', 'abnormal cell'),
(630827, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0101409', 'abnormal perivitelline space', 0.5, 3.6715585125471644, 1.3549093166236559, 'UPHENO:0086172', 'abnormal cell'),
(630828, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0129476', 'decreased size of the wedge region', 0.43243243243243246, 3.6715585125471644, 1.2600400701560144, 'UPHENO:0086172', 'abnormal cell'),
(630829, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0141068', 'abnormally necrotic natural killer cell', 0.4090909090909091, 5.43643956286526, 1.491307481034791, 'HP:0025461', 'Abnormal cell morphology'),
(630830, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0124934', 'absent centrosome', 0.42424242424242425, 3.6715585125471644, 1.2480508339450433, 'UPHENO:0086172', 'abnormal cell'),
(630831, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0115510', 'abnormal degeneration of whole organism', 0.46153846153846156, 2.7446671847279203, 1.125508538339192, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(630832, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0131348', 'abnormally decreased number of absorptive cell', 0.4117647058823529, 3.6715585125471644, 1.229560169755361, 'UPHENO:0086172', 'abnormal cell'),
(630833, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102177', 'abnormal male organism morphology', 0.4444444444444444, 2.7446671847279203, 1.104469140402437, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(630834, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0126314', 'absent absorptive cell', 0.42424242424242425, 3.6715585125471644, 1.2480508339450433, 'UPHENO:0086172', 'abnormal cell'),
(630835, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102286', 'abnormal blastomere V2.1 morphology', 0.43902439024390244, 5.43643956286526, 1.5449043867452603, 'HP:0025461', 'Abnormal cell morphology'),
(630836, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102484', 'abnormal interdigital region morphology', 0.42424242424242425, 2.7446671847279203, 1.0790756508176813, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(630837, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0130899', 'increased size of the microtubule', 0.45714285714285713, 3.6715585125471644, 1.2955411026258445, 'UPHENO:0086172', 'abnormal cell'),
(630838, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0130882', 'increased size of the exocrine cell', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(630839, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0100289', 'abnormal chondroblast', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(630840, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0100784', 'abnormal left blastomere', 0.48148148148148145, 3.6715585125471644, 1.3295816755533123, 'UPHENO:0086172', 'abnormal cell'),
(630841, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0126600', 'abnormally localised progenitor cell', 0.45161290322580644, 3.6715585125471644, 1.2876813267322194, 'UPHENO:0086172', 'abnormal cell'),
(630842, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0140395', 'abnormally necrotic antero-dorsal region', 0.42857142857142855, 2.7446671847279203, 1.0845671654222093, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(630843, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0140104', 'abnormally necrotic circulating cell', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(630844, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0141166', 'abnormally necrotic stage III oocyte', 0.47368421052631576, 5.43643956286526, 1.6047291305419304, 'HP:0025461', 'Abnormal cell morphology'),
(630845, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0103132', 'abnormal endodermal cell morphology', 0.47368421052631576, 5.43643956286526, 1.6047291305419304, 'HP:0025461', 'Abnormal cell morphology'),
(630846, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0130895', 'increased size of the cementoblast', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(630847, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0127217', 'abnormally localised cilium', 0.42424242424242425, 3.6715585125471644, 1.2480508339450433, 'UPHENO:0086172', 'abnormal cell'),
(630848, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0101378', 'abnormal blastomere D1', 0.48148148148148145, 3.6715585125471644, 1.3295816755533123, 'UPHENO:0086172', 'abnormal cell'),
(630849, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0115617', 'abnormally posterioralized primordial germ cell', 0.5142857142857142, 5.43643956286526, 1.6720894724144628, 'HP:0025461', 'Abnormal cell morphology'),
(630850, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0128211', 'decreased size of the progenitor cell', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(630851, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0100675', 'abnormal dorsal vegetal hemisphere blastomere', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(630852, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102336', 'abnormal Merkel cell morphology', 0.6428571428571429, 5.43643956286526, 1.869452862390249, 'HP:0025461', 'Abnormal cell morphology'),
(630853, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0103631', 'abnormally increased number of apoptotic cell', 0.42424242424242425, 3.6715585125471644, 1.2480508339450433, 'UPHENO:0086172', 'abnormal cell'),
(630854, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102069', 'abnormal proepicardium morphology', 0.6, 5.43643956286526, 1.8060630492092893, 'HP:0025461', 'Abnormal cell morphology'),
(630855, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0131626', 'increased size of the adherens junction', 0.45714285714285713, 3.6715585125471644, 1.2955411026258445, 'UPHENO:0086172', 'abnormal cell'),
(630856, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0131666', 'abnormal adherens junction', 0.52, 3.6715585125471644, 1.3817418089225373, 'UPHENO:0086172', 'abnormal cell'),
(630857, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0101192', 'abnormal blastomere D2.1', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(630858, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0101467', 'abnormal alkali secreting cell', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(630859, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102597', 'abnormal blastomere V2.2 morphology', 0.43902439024390244, 5.43643956286526, 1.5449043867452603, 'HP:0025461', 'Abnormal cell morphology'),
(630860, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0107426', 'abnormal yolk platelet morphology', 0.5161290322580645, 3.6715585125471644, 1.376589242279565, 'UPHENO:0086172', 'abnormal cell'),
(630861, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102455', 'abnormal blood morphology', 0.42424242424242425, 2.7446671847279203, 1.0790756508176813, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(630862, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0139780', 'abnormally necrotic neuron', 0.46153846153846156, 5.43643956286526, 1.5840220806831131, 'HP:0025461', 'Abnormal cell morphology'),
(630863, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0100570', 'abnormal axon', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(630864, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0129376', 'decreased size of the lampbrush chromosome', 0.45714285714285713, 3.6715585125471644, 1.2955411026258445, 'UPHENO:0086172', 'abnormal cell'),
(630865, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102113', 'abnormal anatomical line morphology', 0.5217391304347826, 2.7446671847279203, 1.196662137068282, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(630866, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0141296', 'abnormal adherens junction morphology', 0.5517241379310345, 3.6715585125471644, 1.423266473714053, 'UPHENO:0086172', 'abnormal cell'),
(630867, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0128502', 'decreased size of the anatomical line', 0.4444444444444444, 2.7446671847279203, 1.104469140402437, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(630868, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0125384', 'absent ciliated cell', 0.42424242424242425, 3.6715585125471644, 1.2480508339450433, 'UPHENO:0086172', 'abnormal cell'),
(630869, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0141146', 'abnormally necrotic oxygen accumulating cell', 0.5625, 5.43643956286526, 1.748713027947041, 'HP:0025461', 'Abnormal cell morphology'),
(630870, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102147', 'abnormal somatic stem cell morphology', 0.6, 5.43643956286526, 1.8060630492092893, 'HP:0025461', 'Abnormal cell morphology'),
(630871, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0100965', 'abnormal blastomere V2.2', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(630872, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0126548', 'abnormally localised centrosome', 0.4375, 3.6715585125471644, 1.2674016132384338, 'UPHENO:0086172', 'abnormal cell'),
(630873, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0128307', 'decreased size of the oocyte', 0.4186046511627907, 5.43643956286526, 1.5085486027240909, 'HP:0025461', 'Abnormal cell morphology'),
(630874, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0101168', 'abnormal circulating cell', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(630875, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102896', 'abnormal mitotic spindle morphology', 0.5517241379310345, 3.6715585125471644, 1.423266473714053, 'UPHENO:0086172', 'abnormal cell'),
(630876, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0140709', 'abnormally necrotic acid secreting cell', 0.5625, 5.43643956286526, 1.748713027947041, 'HP:0025461', 'Abnormal cell morphology'),
(630877, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0129081', 'decreased size of the multiciliated cell precursor', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(630878, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102608', 'abnormal multiciliated cell morphology', 0.6, 5.43643956286526, 1.8060630492092893, 'HP:0025461', 'Abnormal cell morphology'),
(630879, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0130850', 'increased size of the lampbrush chromosome', 0.45714285714285713, 3.6715585125471644, 1.2955411026258445, 'UPHENO:0086172', 'abnormal cell'),
(630880, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0130352', 'increased size of the ciliary axoneme', 0.43243243243243246, 3.6715585125471644, 1.2600400701560144, 'UPHENO:0086172', 'abnormal cell'),
(630881, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0100429', 'abnormal spermatid', 0.52, 3.6715585125471644, 1.3817418089225373, 'UPHENO:0086172', 'abnormal cell'),
(630882, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102765', 'abnormal motor neuron morphology', 0.4864864864864865, 5.43643956286526, 1.626270082715184, 'HP:0025461', 'Abnormal cell morphology'),
(630883, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102599', 'abnormal blastomere V2.1.2 morphology', 0.43902439024390244, 5.43643956286526, 1.5449043867452603, 'HP:0025461', 'Abnormal cell morphology'),
(630884, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0141154', 'abnormally necrotic barrier cell', 0.5625, 5.43643956286526, 1.748713027947041, 'HP:0025461', 'Abnormal cell morphology'),
(630885, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0100969', 'abnormal disaggregated/reaggregated ectoderm treated with activin', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630886, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0130547', 'increased size of the paracrine cell', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(630887, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0140522', 'abnormally necrotic stage II oocyte', 0.47368421052631576, 5.43643956286526, 1.6047291305419304, 'HP:0025461', 'Abnormal cell morphology'),
(630888, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0129015', 'decreased size of the spermatid', 0.4186046511627907, 5.43643956286526, 1.5085486027240909, 'HP:0025461', 'Abnormal cell morphology'),
(630889, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0101133', 'abnormal motor neuron', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(630890, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0100907', 'abnormal cytoplasm', 0.52, 3.6715585125471644, 1.3817418089225373, 'UPHENO:0086172', 'abnormal cell'),
(630891, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0100702', 'abnormal glial cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(630892, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0100006', 'abnormal anatomical structure', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(630893, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0103093', 'abnormal sperm entry point morphology', 0.5333333333333333, 3.6715585125471644, 1.399344325041251, 'UPHENO:0086172', 'abnormal cell'),
(630894, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0115758', 'abnormally decreased mobility of melanoblast', 0.5185185185185185, 3.6715585125471644, 1.3797721118286204, 'UPHENO:0086172', 'abnormal cell'),
(630895, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0140373', 'abnormally necrotic whole organism', 0.42857142857142855, 2.7446671847279203, 1.0845671654222093, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(630896, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0101074', 'abnormal germinal vesicle', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(630897, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0129582', 'increased size of the portion of organism substance', 0.4444444444444444, 2.7446671847279203, 1.104469140402437, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(630898, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0103041', 'abnormal perivitelline space morphology', 0.5161290322580645, 3.6715585125471644, 1.376589242279565, 'UPHENO:0086172', 'abnormal cell'),
(630899, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0127288', 'abnormally localised pericyte', 0.45161290322580644, 3.6715585125471644, 1.2876813267322194, 'UPHENO:0086172', 'abnormal cell'),
(630900, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0100337', 'abnormal zygote', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(630901, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102281', 'abnormal growth cone morphology', 0.42105263157894735, 3.6715585125471644, 1.2433500608051093, 'UPHENO:0086172', 'abnormal cell'),
(630902, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102977', 'abnormal ascending interneuron morphology', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(630903, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102205', 'abnormal extraembryonic structure morphology', 0.4444444444444444, 2.7446671847279203, 1.104469140402437, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(630904, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0131512', 'absent adherens junction', 0.42424242424242425, 3.6715585125471644, 1.2480508339450433, 'UPHENO:0086172', 'abnormal cell'),
(630905, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0131371', 'abnormally decreased number of electrically active cell', 0.4117647058823529, 3.6715585125471644, 1.229560169755361, 'UPHENO:0086172', 'abnormal cell'),
(630906, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0140663', 'abnormally necrotic right-ventral blastomere', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(630907, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0127338', 'abnormally localised mucus secreting cell', 0.45161290322580644, 3.6715585125471644, 1.2876813267322194, 'UPHENO:0086172', 'abnormal cell'),
(630908, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0101009', 'abnormal blastomere D1.1.1', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(630909, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0142057', 'abnormal desmosome', 0.52, 3.6715585125471644, 1.3817418089225373, 'UPHENO:0086172', 'abnormal cell'),
(630910, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0140610', 'abnormally necrotic blastomere D1', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(630911, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0129487', 'increased size of the anatomical structure', 0.4444444444444444, 2.7446671847279203, 1.104469140402437, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(630912, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0107311', 'abnormal apical junction complex', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(630913, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0127896', 'abnormally localised ring structure', 0.4117647058823529, 3.6715585125471644, 1.229560169755361, 'UPHENO:0086172', 'abnormal cell'),
(630914, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0141123', 'abnormally necrotic microglial cell', 0.42857142857142855, 5.43643956286526, 1.526401870347189, 'HP:0025461', 'Abnormal cell morphology'),
(630915, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0140956', 'abnormally necrotic left-dorsal blastomere', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(630916, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102394', 'abnormal intersomitic region morphology', 0.41379310344827586, 2.7446671847279203, 1.0657036887902793, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(630917, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102276', 'abnormal smooth muscle myocyte morphology', 0.4090909090909091, 5.43643956286526, 1.491307481034791, 'HP:0025461', 'Abnormal cell morphology'),
(630918, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0130964', 'abnormally increased number of cell', 0.45161290322580644, 3.6715585125471644, 1.2876813267322194, 'UPHENO:0086172', 'abnormal cell'),
(630919, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0127168', 'abnormally localised chondroblast', 0.45161290322580644, 3.6715585125471644, 1.2876813267322194, 'UPHENO:0086172', 'abnormal cell'),
(630920, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102533', 'abnormal blastomere D1.2.2 morphology', 0.43902439024390244, 5.43643956286526, 1.5449043867452603, 'HP:0025461', 'Abnormal cell morphology'),
(630921, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0141289', 'abnormal spindle microtubule morphology', 0.5161290322580645, 3.6715585125471644, 1.376589242279565, 'UPHENO:0086172', 'abnormal cell'),
(630922, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0130839', 'increased size of the absorptive cell', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(630923, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0107356', 'abnormal right side morphology', 0.41379310344827586, 2.7446671847279203, 1.0657036887902793, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(630924, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0140366', 'abnormally necrotic left-ventral blastomere', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(630925, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0100887', 'abnormal right-dorsal blastomere', 0.48148148148148145, 3.6715585125471644, 1.3295816755533123, 'UPHENO:0086172', 'abnormal cell'),
(630926, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0126413', 'abnormally localised cell part', 0.4666666666666667, 3.6715585125471644, 1.308966757607698, 'UPHENO:0086172', 'abnormal cell'),
(630927, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102255', 'abnormal olfactory sensory neuron morphology', 0.4090909090909091, 5.43643956286526, 1.491307481034791, 'HP:0025461', 'Abnormal cell morphology'),
(630928, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0103208', 'abnormal blastomere V1.2.2 morphology', 0.43902439024390244, 5.43643956286526, 1.5449043867452603, 'HP:0025461', 'Abnormal cell morphology'),
(630929, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102520', 'abnormal microtubule morphology', 0.5517241379310345, 3.6715585125471644, 1.423266473714053, 'UPHENO:0086172', 'abnormal cell'),
(630930, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0130042', 'increased size of the mesenchymal stem cell', 0.4186046511627907, 5.43643956286526, 1.5085486027240909, 'HP:0025461', 'Abnormal cell morphology'),
(630931, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0131351', 'abnormally decreased number of apoptotic cell', 0.4117647058823529, 3.6715585125471644, 1.229560169755361, 'UPHENO:0086172', 'abnormal cell'),
(630932, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0100715', 'abnormal ciliated cell', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(630933, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0140451', 'abnormally necrotic sensory epithelial cell', 0.47368421052631576, 5.43643956286526, 1.6047291305419304, 'HP:0025461', 'Abnormal cell morphology'),
(630934, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0141091', 'abnormally necrotic posterior region', 0.42857142857142855, 2.7446671847279203, 1.0845671654222093, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(630935, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0128642', 'decreased size of the centrosome', 0.45714285714285713, 3.6715585125471644, 1.2955411026258445, 'UPHENO:0086172', 'abnormal cell'),
(630936, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0100232', 'abnormal lymphatic system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(630937, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0100503', 'abnormal blastomere D2', 0.48148148148148145, 3.6715585125471644, 1.3295816755533123, 'UPHENO:0086172', 'abnormal cell'),
(630938, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0131300', 'abnormally decreased number of alkali secreting cell', 0.4117647058823529, 3.6715585125471644, 1.229560169755361, 'UPHENO:0086172', 'abnormal cell'),
(630939, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0100501', 'abnormal urogenital system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(630940, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0133471', 'abnormally decreased number of cilium in the ciliated cell', 0.4375, 3.6715585125471644, 1.2674016132384338, 'UPHENO:0086172', 'abnormal cell'),
(630941, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0100549', 'abnormal mitotic cell', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(630942, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0131134', 'abnormally increased number of barrier cell', 0.42424242424242425, 3.6715585125471644, 1.2480508339450433, 'UPHENO:0086172', 'abnormal cell'),
(630943, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0101022', 'abnormal blastomere V1.2', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(630944, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102029', 'abnormal ventral vegetal hemisphere blastomere morphology', 0.46153846153846156, 5.43643956286526, 1.5840220806831131, 'HP:0025461', 'Abnormal cell morphology'),
(630945, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0129360', 'decreased size of the vegetal cortex', 0.42105263157894735, 3.6715585125471644, 1.2433500608051093, 'UPHENO:0086172', 'abnormal cell'),
(630946, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0103166', 'abnormal blastomere V2.1.1 morphology', 0.43902439024390244, 5.43643956286526, 1.5449043867452603, 'HP:0025461', 'Abnormal cell morphology'),
(630947, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0130381', 'increased size of the multiciliated cell', 0.4186046511627907, 5.43643956286526, 1.5085486027240909, 'HP:0025461', 'Abnormal cell morphology'),
(630948, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102532', 'abnormal angioblast morphology', 0.5, 5.43643956286526, 1.6487024538808177, 'HP:0025461', 'Abnormal cell morphology'),
(630949, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0103223', 'abnormal xanthophore morphology', 0.4186046511627907, 5.43643956286526, 1.5085486027240909, 'HP:0025461', 'Abnormal cell morphology'),
(630950, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0131180', 'abnormally decreased number of cell', 0.4375, 3.6715585125471644, 1.2674016132384338, 'UPHENO:0086172', 'abnormal cell'),
(630951, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0100032', 'abnormal nervous system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(630952, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0101821', 'abnormal enteroendocrine cell morphology', 0.4864864864864865, 5.43643956286526, 1.626270082715184, 'HP:0025461', 'Abnormal cell morphology'),
(630953, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0101736', 'abnormal embryonic structure morphology', 0.42857142857142855, 2.7446671847279203, 1.0845671654222093, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(630954, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0100108', 'abnormal cell part', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(630955, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0142064', 'abnormal desmosome morphology', 0.5517241379310345, 3.6715585125471644, 1.423266473714053, 'UPHENO:0086172', 'abnormal cell'),
(630956, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0101490', 'abnormal ectodermal cell', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(630957, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0141510', 'abnormal epithelial cell morphology in the foregut endoderm', 0.42857142857142855, 5.43643956286526, 1.526401870347189, 'HP:0025461', 'Abnormal cell morphology'),
(630958, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0131347', 'abnormally decreased number of myelin accumulating cell', 0.4117647058823529, 3.6715585125471644, 1.229560169755361, 'UPHENO:0086172', 'abnormal cell'),
(630959, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102494', 'abnormal blastomere V1 morphology', 0.5294117647058824, 5.43643956286526, 1.696500828969256, 'HP:0025461', 'Abnormal cell morphology'),
(630960, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0125394', 'absent multiciliated cell precursor', 0.42424242424242425, 3.6715585125471644, 1.2480508339450433, 'UPHENO:0086172', 'abnormal cell'),
(630961, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0126725', 'abnormally localised epithelial cell', 0.4117647058823529, 3.6715585125471644, 1.229560169755361, 'UPHENO:0086172', 'abnormal cell'),
(630962, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0140179', 'abnormally necrotic postero-dorsal region', 0.42857142857142855, 2.7446671847279203, 1.0845671654222093, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(630963, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102958', 'abnormal cementoblast morphology', 0.6428571428571429, 5.43643956286526, 1.869452862390249, 'HP:0025461', 'Abnormal cell morphology'),
(630964, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0127821', 'abnormally localised apoptotic cell', 0.45161290322580644, 3.6715585125471644, 1.2876813267322194, 'UPHENO:0086172', 'abnormal cell'),
(630965, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0141023', 'abnormally necrotic ciliated non-epidermal cell', 0.5142857142857142, 5.43643956286526, 1.6720894724144628, 'HP:0025461', 'Abnormal cell morphology'),
(630966, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0128734', 'decreased size of the spermatocyte', 0.4186046511627907, 5.43643956286526, 1.5085486027240909, 'HP:0025461', 'Abnormal cell morphology'),
(630967, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0107347', 'abnormal anterior-posterior axis morphology', 0.4444444444444444, 2.7446671847279203, 1.104469140402437, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(630968, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0101848', 'abnormal hepato-pancreatic progenitor cell morphology', 0.4090909090909091, 5.43643956286526, 1.491307481034791, 'HP:0025461', 'Abnormal cell morphology'),
(630969, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0100864', 'abnormal dorsolateral ascending neuron', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(630970, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0127337', 'abnormally localised oxygen accumulating cell', 0.45161290322580644, 3.6715585125471644, 1.2876813267322194, 'UPHENO:0086172', 'abnormal cell'),
(630971, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102872', 'abnormal ciliated non-epidermal cell morphology', 0.6, 5.43643956286526, 1.8060630492092893, 'HP:0025461', 'Abnormal cell morphology'),
(630972, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0107371', 'abnormal migrating myoblast morphology', 0.6, 5.43643956286526, 1.8060630492092893, 'HP:0025461', 'Abnormal cell morphology'),
(630973, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0128780', 'decreased size of the keratin accumulating cell', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(630974, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102027', 'abnormal blastomere D1.1 morphology', 0.43902439024390244, 5.43643956286526, 1.5449043867452603, 'HP:0025461', 'Abnormal cell morphology'),
(630975, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102474', 'abnormal left-dorsal blastomere morphology', 0.5294117647058824, 5.43643956286526, 1.696500828969256, 'HP:0025461', 'Abnormal cell morphology'),
(630976, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0100398', 'abnormal vegetal blastomere', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(630977, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0131032', 'abnormally increased number of acid secreting cell', 0.42424242424242425, 3.6715585125471644, 1.2480508339450433, 'UPHENO:0086172', 'abnormal cell'),
(630978, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102491', 'abnormal blastomere V1.1.2 morphology', 0.43902439024390244, 5.43643956286526, 1.5449043867452603, 'HP:0025461', 'Abnormal cell morphology'),
(630979, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0140190', 'abnormally necrotic blastomere V2', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(630980, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102176', 'abnormal neuromast support cell morphology', 0.43902439024390244, 5.43643956286526, 1.5449043867452603, 'HP:0025461', 'Abnormal cell morphology'),
(630981, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0140167', 'abnormally necrotic medial region', 0.41379310344827586, 2.7446671847279203, 1.0657036887902793, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(630982, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102181', 'abnormal mitotic cell morphology', 0.6428571428571429, 5.43643956286526, 1.869452862390249, 'HP:0025461', 'Abnormal cell morphology'),
(630983, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0131589', 'decreased size of the actin cytoskeleton', 0.45714285714285713, 3.6715585125471644, 1.2955411026258445, 'UPHENO:0086172', 'abnormal cell'),
(630984, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0101325', 'abnormal blastomere D2.1.1', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(630985, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0125724', 'absent polar body', 0.4117647058823529, 3.6715585125471644, 1.229560169755361, 'UPHENO:0086172', 'abnormal cell'),
(630986, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0125854', 'absent barrier epithelial cell', 0.42424242424242425, 3.6715585125471644, 1.2480508339450433, 'UPHENO:0086172', 'abnormal cell'),
(630987, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0131677', 'abnormal actin filament', 0.5, 3.6715585125471644, 1.3549093166236559, 'UPHENO:0086172', 'abnormal cell'),
(630988, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0107412', 'abnormal adult thrombocyte morphology', 0.4090909090909091, 5.43643956286526, 1.491307481034791, 'HP:0025461', 'Abnormal cell morphology'),
(630989, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0140803', 'abnormally necrotic pericyte', 0.5625, 5.43643956286526, 1.748713027947041, 'HP:0025461', 'Abnormal cell morphology'),
(630990, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102307', 'abnormal dorsal vegetal hemisphere blastomere morphology', 0.46153846153846156, 5.43643956286526, 1.5840220806831131, 'HP:0025461', 'Abnormal cell morphology'),
(630991, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0129438', 'decreased size of the mitotic cell', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(630992, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0130465', 'increased size of the migrating myoblast', 0.4186046511627907, 5.43643956286526, 1.5085486027240909, 'HP:0025461', 'Abnormal cell morphology'),
(630993, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0101374', 'abnormal migratory neural crest cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(630994, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0107357', 'abnormal proximal-distal axis morphology', 0.4444444444444444, 2.7446671847279203, 1.104469140402437, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(630995, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0100004', 'abnormal cell', 0.5652173913043478, 3.6715585125471644, 1.440565418328227, 'UPHENO:0086172', 'abnormal cell'),
(630996, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0131278', 'abnormally decreased number of keratin accumulating cell', 0.4117647058823529, 3.6715585125471644, 1.229560169755361, 'UPHENO:0086172', 'abnormal cell'),
(630997, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0101480', 'abnormal stage V oocyte', 0.5, 3.6715585125471644, 1.3549093166236559, 'UPHENO:0086172', 'abnormal cell'),
(630998, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0131130', 'abnormally increased number of myelin accumulating cell', 0.42424242424242425, 3.6715585125471644, 1.2480508339450433, 'UPHENO:0086172', 'abnormal cell'),
(630999, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0128336', 'decreased size of the proepicardium', 0.4186046511627907, 5.43643956286526, 1.5085486027240909, 'HP:0025461', 'Abnormal cell morphology'),
(631000, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0131247', 'abnormally decreased number of nucleate erythrocyte', 0.4117647058823529, 3.6715585125471644, 1.229560169755361, 'UPHENO:0086172', 'abnormal cell'),
(631001, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0101642', 'abnormal multicellular anatomical structure morphology', 0.46153846153846156, 2.7446671847279203, 1.125508538339192, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(631002, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0129879', 'increased size of the pericyte', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(631003, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0130615', 'increased size of the kinetochore', 0.45714285714285713, 3.6715585125471644, 1.2955411026258445, 'UPHENO:0086172', 'abnormal cell'),
(631004, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0130333', 'increased size of the endoplasmic reticulum', 0.45714285714285713, 3.6715585125471644, 1.2955411026258445, 'UPHENO:0086172', 'abnormal cell'),
(631005, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0133483', 'increased size of the cilium in multiciliated cell', 0.41025641025641024, 3.6715585125471644, 1.2273061620492112, 'UPHENO:0086172', 'abnormal cell'),
(631006, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0140938', 'abnormally necrotic secretory epithelial cell', 0.47368421052631576, 5.43643956286526, 1.6047291305419304, 'HP:0025461', 'Abnormal cell morphology'),
(631007, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0126159', 'absent apoptotic cell', 0.42424242424242425, 3.6715585125471644, 1.2480508339450433, 'UPHENO:0086172', 'abnormal cell'),
(631008, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0131066', 'abnormally increased number of myoblast', 0.42424242424242425, 3.6715585125471644, 1.2480508339450433, 'UPHENO:0086172', 'abnormal cell'),
(631009, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0103104', 'abnormal zygote cortex morphology', 0.5333333333333333, 3.6715585125471644, 1.399344325041251, 'UPHENO:0086172', 'abnormal cell'),
(631010, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0140781', 'abnormally necrotic stage I oocyte', 0.47368421052631576, 5.43643956286526, 1.6047291305419304, 'HP:0025461', 'Abnormal cell morphology'),
(631011, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102364', 'abnormal tendon fibroblast morphology', 0.42857142857142855, 5.43643956286526, 1.526401870347189, 'HP:0025461', 'Abnormal cell morphology'),
(631012, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0100843', 'abnormal fasciculated network of fibrils', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(631013, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102636', 'abnormal acid secreting cell morphology', 0.6428571428571429, 5.43643956286526, 1.869452862390249, 'HP:0025461', 'Abnormal cell morphology'),
(631014, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0130979', 'abnormally increased number of Merkel cell', 0.42424242424242425, 3.6715585125471644, 1.2480508339450433, 'UPHENO:0086172', 'abnormal cell'),
(631015, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0101641', 'abnormal multi-tissue structure morphology', 0.42857142857142855, 2.7446671847279203, 1.0845671654222093, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(631016, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0141239', 'abnormally necrotic neural progenitor cell', 0.42857142857142855, 5.43643956286526, 1.526401870347189, 'HP:0025461', 'Abnormal cell morphology'),
(631017, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102333', 'abnormal microglial cell morphology', 0.4864864864864865, 5.43643956286526, 1.626270082715184, 'HP:0025461', 'Abnormal cell morphology'),
(631018, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0126454', 'abnormally localised stem cell', 0.45161290322580644, 3.6715585125471644, 1.2876813267322194, 'UPHENO:0086172', 'abnormal cell'),
(631019, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0128737', 'decreased size of the perivitelline space', 0.43243243243243246, 3.6715585125471644, 1.2600400701560144, 'UPHENO:0086172', 'abnormal cell'),
(631020, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0103019', 'abnormal melanophore morphology', 0.4186046511627907, 5.43643956286526, 1.5085486027240909, 'HP:0025461', 'Abnormal cell morphology'),
(631021, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0126982', 'abnormally localised secondary oogonium', 0.42424242424242425, 3.6715585125471644, 1.2480508339450433, 'UPHENO:0086172', 'abnormal cell'),
(631022, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102504', 'abnormal neuroendocrine cell morphology', 0.4864864864864865, 5.43643956286526, 1.626270082715184, 'HP:0025461', 'Abnormal cell morphology'),
(631023, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102081', 'abnormal lymphocyte morphology', 0.5294117647058824, 5.43643956286526, 1.696500828969256, 'HP:0025461', 'Abnormal cell morphology'),
(631024, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0100509', 'abnormal germ plasm', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(631025, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0130074', 'increased size of the ciliated cell', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(631026, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102365', 'abnormal fibroblast morphology', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(631027, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0131599', 'decreased size of the actin filament', 0.4444444444444444, 3.6715585125471644, 1.2774207542365574, 'UPHENO:0086172', 'abnormal cell'),
(631028, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0133473', 'abnormally decreased number of cilium in the ciliated non-epidermal cell', 0.4117647058823529, 3.6715585125471644, 1.229560169755361, 'UPHENO:0086172', 'abnormal cell'),
(631029, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0100900', 'abnormal angioblast', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(631030, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0125868', 'absent cementoblast', 0.42424242424242425, 3.6715585125471644, 1.2480508339450433, 'UPHENO:0086172', 'abnormal cell'),
(631031, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102109', 'abnormal pericyte morphology', 0.6428571428571429, 5.43643956286526, 1.869452862390249, 'HP:0025461', 'Abnormal cell morphology'),
(631032, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0129263', 'decreased size of the mitochondrial cloud', 0.43243243243243246, 3.6715585125471644, 1.2600400701560144, 'UPHENO:0086172', 'abnormal cell'),
(631033, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0103430', 'decreased size of the apical junction complex', 0.41025641025641024, 3.6715585125471644, 1.2273061620492112, 'UPHENO:0086172', 'abnormal cell'),
(631034, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0107351', 'abnormal anterior side morphology', 0.41379310344827586, 2.7446671847279203, 1.0657036887902793, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(631035, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0101500', 'abnormal endodermal cell', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(631036, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0129087', 'decreased size of the ciliated non-epidermal cell', 0.4186046511627907, 5.43643956286526, 1.5085486027240909, 'HP:0025461', 'Abnormal cell morphology'),
(631037, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0128911', 'decreased size of the barrier cell', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(631038, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102323', 'abnormal keratin accumulating cell morphology', 0.6428571428571429, 5.43643956286526, 1.869452862390249, 'HP:0025461', 'Abnormal cell morphology'),
(631039, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0101828', 'abnormal neuron morphology', 0.5142857142857142, 5.43643956286526, 1.6720894724144628, 'HP:0025461', 'Abnormal cell morphology'),
(631040, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0125997', 'absent Merkel cell', 0.42424242424242425, 3.6715585125471644, 1.2480508339450433, 'UPHENO:0086172', 'abnormal cell'),
(631041, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0125833', 'absent kinetochore', 0.42424242424242425, 3.6715585125471644, 1.2480508339450433, 'UPHENO:0086172', 'abnormal cell'),
(631042, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0130116', 'increased size of the secondary spermatogonium', 0.4186046511627907, 5.43643956286526, 1.5085486027240909, 'HP:0025461', 'Abnormal cell morphology'),
(631043, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0141478', 'abnormally necrotic lymphoblast', 0.47368421052631576, 5.43643956286526, 1.6047291305419304, 'HP:0025461', 'Abnormal cell morphology'),
(631044, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0103084', 'abnormal blastomere V1.1.1 morphology', 0.43902439024390244, 5.43643956286526, 1.5449043867452603, 'HP:0025461', 'Abnormal cell morphology'),
(631045, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0131635', 'increased size of the spindle microtubule', 0.42105263157894735, 3.6715585125471644, 1.2433500608051093, 'UPHENO:0086172', 'abnormal cell'),
(631046, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102621', 'abnormal right blastomere morphology', 0.5294117647058824, 5.43643956286526, 1.696500828969256, 'HP:0025461', 'Abnormal cell morphology'),
(631047, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0131145', 'abnormally increased number of polar body', 0.42424242424242425, 3.6715585125471644, 1.2480508339450433, 'UPHENO:0086172', 'abnormal cell'),
(631048, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0129571', 'increased size of the anatomical region', 0.41379310344827586, 2.7446671847279203, 1.0657036887902793, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(631049, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0107410', 'abnormal thrombocyte morphology', 0.42857142857142855, 5.43643956286526, 1.526401870347189, 'HP:0025461', 'Abnormal cell morphology'),
(631050, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0107359', 'abnormal axial region morphology', 0.4444444444444444, 2.7446671847279203, 1.104469140402437, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(631051, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0103179', 'abnormal lampbrush chromosome morphology', 0.5517241379310345, 3.6715585125471644, 1.423266473714053, 'UPHENO:0086172', 'abnormal cell'),
(631052, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0131607', 'decreased size of the cortical actin cytoskeleton', 0.4444444444444444, 3.6715585125471644, 1.2774207542365574, 'UPHENO:0086172', 'abnormal cell'),
(631053, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0131669', 'abnormal Roux spot', 0.48148148148148145, 3.6715585125471644, 1.3295816755533123, 'UPHENO:0086172', 'abnormal cell'),
(631054, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0140708', 'abnormally necrotic hatching gland cell', 0.4090909090909091, 5.43643956286526, 1.491307481034791, 'HP:0025461', 'Abnormal cell morphology'),
(631055, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0129486', 'increased size of the cell', 0.4864864864864865, 5.43643956286526, 1.626270082715184, 'HP:0025461', 'Abnormal cell morphology'),
(631056, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0140267', 'abnormally necrotic multiciliated cell', 0.5142857142857142, 5.43643956286526, 1.6720894724144628, 'HP:0025461', 'Abnormal cell morphology'),
(631057, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0101850', 'abnormal epithelial cell morphology', 0.5806451612903226, 5.43643956286526, 1.776694213089295, 'HP:0025461', 'Abnormal cell morphology'),
(631058, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0103753', 'increased size of the apical junction complex', 0.41025641025641024, 3.6715585125471644, 1.2273061620492112, 'UPHENO:0086172', 'abnormal cell'),
(631059, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0127979', 'abnormally localised absorptive cell', 0.45161290322580644, 3.6715585125471644, 1.2876813267322194, 'UPHENO:0086172', 'abnormal cell'),
(631060, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0139992', 'abnormally necrotic gamete', 0.4090909090909091, 5.43643956286526, 1.491307481034791, 'HP:0025461', 'Abnormal cell morphology'),
(631061, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0100626', 'abnormal primordial germ cell', 0.52, 3.6715585125471644, 1.3817418089225373, 'UPHENO:0086172', 'abnormal cell'),
(631062, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0139929', 'abnormally necrotic barrier epithelial cell', 0.5625, 5.43643956286526, 1.748713027947041, 'HP:0025461', 'Abnormal cell morphology'),
(631063, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102024', 'abnormal cilium morphology', 0.5333333333333333, 3.6715585125471644, 1.399344325041251, 'UPHENO:0086172', 'abnormal cell'),
(631064, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0130212', 'increased size of the spermatocyte', 0.4186046511627907, 5.43643956286526, 1.5085486027240909, 'HP:0025461', 'Abnormal cell morphology'),
(631065, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0125115', 'absent paracrine cell', 0.42424242424242425, 3.6715585125471644, 1.2480508339450433, 'UPHENO:0086172', 'abnormal cell'),
(631066, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0101694', 'abnormal anatomical space morphology', 0.48, 2.7446671847279203, 1.1477979999413668, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(631067, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102704', 'abnormal mitochondrial cloud morphology', 0.5161290322580645, 3.6715585125471644, 1.376589242279565, 'UPHENO:0086172', 'abnormal cell'),
(631068, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0133438', 'abnormal cilium morphology in the ciliated non-epidermal cell', 0.5, 3.6715585125471644, 1.3549093166236559, 'UPHENO:0086172', 'abnormal cell'),
(631069, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0101664', 'abnormal nervous system morphology', 0.4117647058823529, 2.7446671847279203, 1.0630884610720022, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(631070, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0100842', 'abnormal left-dorsal blastomere', 0.48148148148148145, 3.6715585125471644, 1.3295816755533123, 'UPHENO:0086172', 'abnormal cell'),
(631071, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0140767', 'abnormally necrotic stage IV oocyte', 0.47368421052631576, 5.43643956286526, 1.6047291305419304, 'HP:0025461', 'Abnormal cell morphology'),
(631072, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0101948', 'abnormal gamete morphology', 0.46153846153846156, 5.43643956286526, 1.5840220806831131, 'HP:0025461', 'Abnormal cell morphology'),
(631073, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0131513', 'absent actin cytoskeleton', 0.42424242424242425, 3.6715585125471644, 1.2480508339450433, 'UPHENO:0086172', 'abnormal cell'),
(631074, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0131675', 'abnormal spindle microtubule', 0.5, 3.6715585125471644, 1.3549093166236559, 'UPHENO:0086172', 'abnormal cell'),
(631075, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0103146', 'abnormal dendrite morphology', 0.41025641025641024, 3.6715585125471644, 1.2273061620492112, 'UPHENO:0086172', 'abnormal cell'),
(631076, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102588', 'abnormal centrosome morphology', 0.5517241379310345, 3.6715585125471644, 1.423266473714053, 'UPHENO:0086172', 'abnormal cell'),
(631077, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0139734', 'abnormally necrotic blastomere', 0.4864864864864865, 5.43643956286526, 1.626270082715184, 'HP:0025461', 'Abnormal cell morphology'),
(631078, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102434', 'abnormal exocrine cell morphology', 0.6428571428571429, 5.43643956286526, 1.869452862390249, 'HP:0025461', 'Abnormal cell morphology'),
(631079, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102739', 'abnormal erythroid cell morphology', 0.5294117647058824, 5.43643956286526, 1.696500828969256, 'HP:0025461', 'Abnormal cell morphology'),
(631080, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0128267', 'decreased size of the zygote', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(631081, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0101504', 'abnormal blastomere D2.2.1', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(631082, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102869', 'abnormal mucus secreting cell morphology', 0.6428571428571429, 5.43643956286526, 1.869452862390249, 'HP:0025461', 'Abnormal cell morphology'),
(631083, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0130043', 'increased size of the primordial germ cell', 0.4186046511627907, 5.43643956286526, 1.5085486027240909, 'HP:0025461', 'Abnormal cell morphology'),
(631084, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0103219', 'abnormal hemangioblast morphology', 0.5294117647058824, 5.43643956286526, 1.696500828969256, 'HP:0025461', 'Abnormal cell morphology'),
(631085, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0100395', 'abnormal blastomere D1.1', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(631086, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0126473', 'abnormally localised germ cell', 0.45161290322580644, 3.6715585125471644, 1.2876813267322194, 'UPHENO:0086172', 'abnormal cell'),
(631087, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0127703', 'abnormally localised morula cell', 0.4117647058823529, 3.6715585125471644, 1.229560169755361, 'UPHENO:0086172', 'abnormal cell'),
(631088, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0107398', 'abnormal apical junction complex morphology', 0.48484848484848486, 3.6715585125471644, 1.3342224633999569, 'UPHENO:0086172', 'abnormal cell'),
(631089, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0100954', 'abnormal neural progenitor cell', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(631090, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0107352', 'abnormal posterior side morphology', 0.41379310344827586, 2.7446671847279203, 1.0657036887902793, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(631091, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0103894', 'abnormally decreased number of spindle microtubule', 0.4375, 3.6715585125471644, 1.2674016132384338, 'UPHENO:0086172', 'abnormal cell'),
(631092, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102213', 'abnormal immune system morphology', 0.42424242424242425, 2.7446671847279203, 1.0790756508176813, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(631093, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0100392', 'abnormal cilium', 0.5, 3.6715585125471644, 1.3549093166236559, 'UPHENO:0086172', 'abnormal cell'),
(631094, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0101345', 'abnormal ascending interneuron', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(631095, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0133449', 'decreased size of the cilium in the multiciliated cell', 0.41025641025641024, 3.6715585125471644, 1.2273061620492112, 'UPHENO:0086172', 'abnormal cell'),
(631096, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0107354', 'abnormal ventral side morphology', 0.41379310344827586, 2.7446671847279203, 1.0657036887902793, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(631097, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0100175', 'abnormal migrating neuroblast', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(631098, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0100551', 'abnormal oocyte cortex', 0.48148148148148145, 3.6715585125471644, 1.3295816755533123, 'UPHENO:0086172', 'abnormal cell'),
(631099, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0139969', 'abnormally necrotic primordial germ cell', 0.5142857142857142, 5.43643956286526, 1.6720894724144628, 'HP:0025461', 'Abnormal cell morphology'),
(631100, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0139901', 'abnormally necrotic enteroendocrine cell', 0.42857142857142855, 5.43643956286526, 1.526401870347189, 'HP:0025461', 'Abnormal cell morphology'),
(631101, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0100872', 'abnormal neuroendocrine cell', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(631102, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0129425', 'decreased size of the microtubule', 0.45714285714285713, 3.6715585125471644, 1.2955411026258445, 'UPHENO:0086172', 'abnormal cell'),
(631103, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0127343', 'abnormally localised filopodium', 0.4375, 3.6715585125471644, 1.2674016132384338, 'UPHENO:0086172', 'abnormal cell'),
(631104, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0100899', 'abnormal secondary spermatogonium', 0.52, 3.6715585125471644, 1.3817418089225373, 'UPHENO:0086172', 'abnormal cell'),
(631105, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0101702', 'abnormal anatomical system morphology', 0.42857142857142855, 2.7446671847279203, 1.0845671654222093, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(631106, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0130834', 'increased size of the vegetal cortex', 0.42105263157894735, 3.6715585125471644, 1.2433500608051093, 'UPHENO:0086172', 'abnormal cell'),
(631107, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0127815', 'abnormally localised ciliated non-epidermal cell', 0.42424242424242425, 3.6715585125471644, 1.2480508339450433, 'UPHENO:0086172', 'abnormal cell'),
(631108, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0100993', 'abnormal ligament cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(631109, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0141048', 'abnormally necrotic mitotic cell', 0.5625, 5.43643956286526, 1.748713027947041, 'HP:0025461', 'Abnormal cell morphology'),
(631110, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0139888', 'abnormally necrotic glial cell', 0.46153846153846156, 5.43643956286526, 1.5840220806831131, 'HP:0025461', 'Abnormal cell morphology'),
(631111, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0101834', 'abnormal embryo morphology', 0.42857142857142855, 2.7446671847279203, 1.0845671654222093, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(631112, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102353', 'abnormal centromere morphology', 0.5517241379310345, 3.6715585125471644, 1.423266473714053, 'UPHENO:0086172', 'abnormal cell'),
(631113, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102270', 'abnormal polar body morphology', 0.46153846153846156, 5.43643956286526, 1.5840220806831131, 'HP:0025461', 'Abnormal cell morphology'),
(631114, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102943', 'abnormal bottle cell morphology', 0.5294117647058824, 5.43643956286526, 1.696500828969256, 'HP:0025461', 'Abnormal cell morphology'),
(631115, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0127740', 'abnormally localised yolk platelet', 0.4117647058823529, 3.6715585125471644, 1.229560169755361, 'UPHENO:0086172', 'abnormal cell'),
(631116, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0100989', 'abnormal right blastomere', 0.48148148148148145, 3.6715585125471644, 1.3295816755533123, 'UPHENO:0086172', 'abnormal cell'),
(631117, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0101835', 'abnormal endocrine cell morphology', 0.5142857142857142, 5.43643956286526, 1.6720894724144628, 'HP:0025461', 'Abnormal cell morphology'),
(631118, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0142065', 'abnormally decreased number of desmosome', 0.45161290322580644, 3.6715585125471644, 1.2876813267322194, 'UPHENO:0086172', 'abnormal cell'),
(631119, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102832', 'abnormal joint region morphology', 0.4444444444444444, 2.7446671847279203, 1.104469140402437, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(631120, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0100218', 'abnormal epithelial cell', 0.48148148148148145, 3.6715585125471644, 1.3295816755533123, 'UPHENO:0086172', 'abnormal cell'),
(631121, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0124984', 'absent progenitor cell', 0.42424242424242425, 3.6715585125471644, 1.2480508339450433, 'UPHENO:0086172', 'abnormal cell'),
(631122, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0101638', 'abnormal anatomical structure morphology', 0.5217391304347826, 2.7446671847279203, 1.196662137068282, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(631123, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102028', 'abnormal dorsal animal hemisphere blastomere morphology', 0.46153846153846156, 5.43643956286526, 1.5840220806831131, 'HP:0025461', 'Abnormal cell morphology'),
(631124, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102258', 'abnormal primordial germ cell morphology', 0.6, 5.43643956286526, 1.8060630492092893, 'HP:0025461', 'Abnormal cell morphology'),
(631125, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0128988', 'decreased size of the migrating myoblast', 0.4186046511627907, 5.43643956286526, 1.5085486027240909, 'HP:0025461', 'Abnormal cell morphology'),
(631126, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0101897', 'abnormal sensory epithelial cell morphology', 0.5454545454545454, 5.43643956286526, 1.7220135512398786, 'HP:0025461', 'Abnormal cell morphology'),
(631127, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0139886', 'abnormally necrotic process', 0.41379310344827586, 2.7446671847279203, 1.0657036887902793, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(631128, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0131195', 'abnormally decreased number of Merkel cell', 0.4117647058823529, 3.6715585125471644, 1.229560169755361, 'UPHENO:0086172', 'abnormal cell'),
(631129, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0127476', 'abnormally localised nucleus', 0.4375, 3.6715585125471644, 1.2674016132384338, 'UPHENO:0086172', 'abnormal cell'),
(631130, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0107350', 'abnormal anatomical side morphology', 0.4444444444444444, 2.7446671847279203, 1.104469140402437, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(631131, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0103756', 'increased size of the germ cell', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(631132, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0101463', 'abnormal right-ventral blastomere', 0.48148148148148145, 3.6715585125471644, 1.3295816755533123, 'UPHENO:0086172', 'abnormal cell'),
(631133, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0103145', 'abnormal basal body morphology', 0.5517241379310345, 3.6715585125471644, 1.423266473714053, 'UPHENO:0086172', 'abnormal cell'),
(631134, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0101871', 'abnormal acellular anatomical structure morphology', 0.46153846153846156, 2.7446671847279203, 1.125508538339192, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(631135, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0141007', 'abnormally necrotic electrically active cell', 0.5625, 5.43643956286526, 1.748713027947041, 'HP:0025461', 'Abnormal cell morphology'),
(631136, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0126472', 'abnormally localised secondary spermatogonium', 0.42424242424242425, 3.6715585125471644, 1.2480508339450433, 'UPHENO:0086172', 'abnormal cell'),
(631137, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0103005', 'abnormal oxygen accumulating cell morphology', 0.6428571428571429, 5.43643956286526, 1.869452862390249, 'HP:0025461', 'Abnormal cell morphology'),
(631138, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0103126', 'abnormal blastomere D1.2.1 morphology', 0.43902439024390244, 5.43643956286526, 1.5449043867452603, 'HP:0025461', 'Abnormal cell morphology'),
(631139, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0101311', 'abnormal bottle cell', 0.48148148148148145, 3.6715585125471644, 1.3295816755533123, 'UPHENO:0086172', 'abnormal cell'),
(631140, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0101575', 'abnormal vitelline membrane', 0.48148148148148145, 3.6715585125471644, 1.3295816755533123, 'UPHENO:0086172', 'abnormal cell'),
(631141, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0101132', 'abnormal apoptotic cell', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(631142, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0140364', 'abnormally necrotic anterior region', 0.42857142857142855, 2.7446671847279203, 1.0845671654222093, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(631143, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0142043', 'decreased size of the desmosome', 0.45714285714285713, 3.6715585125471644, 1.2955411026258445, 'UPHENO:0086172', 'abnormal cell'),
(631144, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0100081', 'abnormal anatomical entity in vitro', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(631145, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0128874', 'decreased size of the ciliary axoneme', 0.43243243243243246, 3.6715585125471644, 1.2600400701560144, 'UPHENO:0086172', 'abnormal cell'),
(631146, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0100721', 'abnormal centromere', 0.52, 3.6715585125471644, 1.3817418089225373, 'UPHENO:0086172', 'abnormal cell'),
(631147, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0141504', 'abnormal axon microtubule bundle morphology', 0.41025641025641024, 3.6715585125471644, 1.2273061620492112, 'UPHENO:0086172', 'abnormal cell'),
(631148, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0100862', 'abnormal blastomere V1', 0.48148148148148145, 3.6715585125471644, 1.3295816755533123, 'UPHENO:0086172', 'abnormal cell'),
(631149, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0100547', 'abnormal blastomere V2', 0.48148148148148145, 3.6715585125471644, 1.3295816755533123, 'UPHENO:0086172', 'abnormal cell'),
(631150, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0107345', 'abnormal anatomical axis morphology', 0.48, 2.7446671847279203, 1.1477979999413668, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(631151, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0127364', 'abnormally localised multiciliated cell', 0.42424242424242425, 3.6715585125471644, 1.2480508339450433, 'UPHENO:0086172', 'abnormal cell'),
(631152, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0131687', 'abnormal astral microtubule', 0.48148148148148145, 3.6715585125471644, 1.3295816755533123, 'UPHENO:0086172', 'abnormal cell'),
(631153, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0124716', 'absent cell', 0.45161290322580644, 3.6715585125471644, 1.2876813267322194, 'UPHENO:0086172', 'abnormal cell'),
(631154, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102189', 'abnormal prime meridian morphology', 0.41379310344827586, 2.7446671847279203, 1.0657036887902793, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(631155, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0131165', 'abnormally increased number of cementoblast', 0.42424242424242425, 3.6715585125471644, 1.2480508339450433, 'UPHENO:0086172', 'abnormal cell'),
(631156, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102347', 'abnormal ciliated cell morphology', 0.6428571428571429, 5.43643956286526, 1.869452862390249, 'HP:0025461', 'Abnormal cell morphology'),
(631157, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0127508', 'abnormally localised barrier epithelial cell', 0.45161290322580644, 3.6715585125471644, 1.2876813267322194, 'UPHENO:0086172', 'abnormal cell'),
(631158, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102648', 'abnormal egg morphology', 0.43902439024390244, 5.43643956286526, 1.5449043867452603, 'HP:0025461', 'Abnormal cell morphology'),
(631159, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0131346', 'abnormally decreased number of chondroblast', 0.4117647058823529, 3.6715585125471644, 1.229560169755361, 'UPHENO:0086172', 'abnormal cell'),
(631160, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0100638', 'abnormal polar body', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(631161, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0129747', 'increased size of the zygote', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(631162, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0127520', 'abnormally localised gastrula cell', 0.4117647058823529, 3.6715585125471644, 1.229560169755361, 'UPHENO:0086172', 'abnormal cell'),
(631163, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0125715', 'absent barrier cell', 0.42424242424242425, 3.6715585125471644, 1.2480508339450433, 'UPHENO:0086172', 'abnormal cell'),
(631164, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0140471', 'abnormally necrotic multiciliated cell precursor', 0.5625, 5.43643956286526, 1.748713027947041, 'HP:0025461', 'Abnormal cell morphology'),
(631165, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0140095', 'abnormally necrotic bottle cell', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(631166, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0102641', 'abnormal blastomere D1.1.1 morphology', 0.43902439024390244, 5.43643956286526, 1.5449043867452603, 'HP:0025461', 'Abnormal cell morphology'),
(631167, 'HP:0034552', 'Abnormal peroxisomal morphology', 'XPO:0127339', 'abnormally localised migrating myoblast', 0.42424242424242425, 3.6715585125471644, 1.2480508339450433, 'UPHENO:0086172', 'abnormal cell'),
