(177849, 'HP:0011926', 'Proximal placement of hallux', 'XPO:0129977', 'increased size of the digit-joint region', 0.4533333333333333, 6.466375519622663, 1.7121400552804105, 'UPHENO:0086700', 'abnormal digit morphology'),
(177850, 'HP:0011926', 'Proximal placement of hallux', 'XPO:0133379', 'fused hindlimb digits part of regenerating hindlimb', 0.42424242424242425, 7.639349617137506, 1.800260037108487, 'HP:0001780', 'Abnormal toe morphology'),
(177851, 'HP:0011926', 'Proximal placement of hallux', 'XPO:0129321', 'decreased size of the hindlimb digit 4', 0.4375, 7.639349617137506, 1.8281727099750884, 'UPHENO:0088132', 'abnormal pedal digit morphology'),
(177852, 'HP:0011926', 'Proximal placement of hallux', 'XPO:0103778', 'decreased size of the hindlimb digit in the regenerating hindlimb', 0.42, 7.639349617137506, 1.791236120448042, 'HP:0001780', 'Abnormal toe morphology'),
(177853, 'HP:0011926', 'Proximal placement of hallux', 'XPO:0103191', 'abnormal claw of hindlimb digit 5 morphology', 0.4117647058823529, 7.639349617137506, 1.773588043552699, 'UPHENO:0088132', 'abnormal pedal digit morphology'),
(177854, 'HP:0011926', 'Proximal placement of hallux', 'XPO:0128670', 'decreased size of the claw primordium', 0.47191011235955055, 7.639349617137506, 1.8987064902657413, 'HP:0001780', 'Abnormal toe morphology'),
(177855, 'HP:0011926', 'Proximal placement of hallux', 'XPO:0141208', 'abnormally necrotic digit-joint region', 0.4657534246575342, 6.466375519622663, 1.7354355486119033, 'UPHENO:0086700', 'abnormal digit morphology'),
(177856, 'HP:0011926', 'Proximal placement of hallux', 'XPO:0102457', 'abnormal claw of hindlimb digit 2 morphology', 0.4117647058823529, 7.639349617137506, 1.773588043552699, 'UPHENO:0088132', 'abnormal pedal digit morphology'),
(177857, 'HP:0031031', 'Abnormal retinol-binding protein level', 'XPO:0141873', 'abnormal tricarboxylic acid metabolic process', 0.4339622641509434, 7.41682187759612, 1.7940515084037758, 'HP:0430071', 'Abnormal circulating organic compound concentration'),
(177858, 'HP:0031031', 'Abnormal retinol-binding protein level', 'XPO:0141869', 'abnormal alpha-amino acid metabolic process', 0.40350877192982454, 7.41682187759612, 1.729957423594889, 'HP:0430071', 'Abnormal circulating organic compound concentration'),
(177859, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0101221', 'abnormal larval immune system', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(177860, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0101326', 'abnormal cementoblast', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(177861, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0141271', 'increased surface breathing', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(177862, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0107258', 'abnormal anatomical axis', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(177863, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0101373', 'abnormal oxygen accumulating cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(177864, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0100062', 'abnormal anatomical space', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(177865, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0141775', 'abnormal nitrogen compound metabolic process', 0.5238095238095238, 4.758907843651163, 1.5788480773767701, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(177866, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0100888', 'abnormal microtubule', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(177867, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0101467', 'abnormal alkali secreting cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(177868, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0100715', 'abnormal ciliated cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(177869, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0141267', 'abnormal resting posture', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(177870, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0100477', 'abnormal pericyte', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(177871, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0141754', 'abnormal homeostatic process', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(177872, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0141738', 'abnormal carbon dioxide homeostasis', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(177873, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0100481', 'abnormal anatomical line', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(177874, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0101333', 'abnormal barrier epithelial cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(177875, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0101547', 'abnormal lampbrush chromosome', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(177876, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0100031', 'abnormal central nervous system', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(177877, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0131691', 'abnormal molecular function', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(177878, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0107312', 'abnormal filopodium', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(177879, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0107253', 'abnormal enteric nervous system', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(177880, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0101132', 'abnormal apoptotic cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(177881, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0100549', 'abnormal mitotic cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(177882, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0141788', 'abnormal hormone biosynthetic process', 0.44, 4.758907843651163, 1.447038165082909, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(177883, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0133403', 'abnormal developmental process', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(177884, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0100225', 'abnormal endocrine system', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(177885, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0141790', 'abnormal cellular metabolic process', 0.5, 4.758907843651163, 1.5425478669479211, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(177886, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0101109', 'abnormal egg cell-free extract', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(177887, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0107261', 'abnormal dorsal-ventral axis', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(177888, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0101569', 'abnormal activin-induced ectoderm', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(177889, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0107262', 'abnormal left-right axis', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(177890, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0101228', 'abnormal mesenchymal stem cell', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(177891, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0100917', 'abnormal stage III oocyte', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(177892, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0100626', 'abnormal primordial germ cell', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(177893, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0100724', 'abnormal kinetochore', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(177894, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0100704', 'abnormal Merkel cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(177895, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0100802', 'abnormal exocrine cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(177896, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0100202', 'abnormal embryo', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(177897, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0141776', 'abnormal metabolic process', 0.5789473684210527, 4.758907843651163, 1.6598666129060333, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(177898, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0141748', 'abnormal gas homeostasis', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(177899, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0101241', 'abnormal nucleate erythrocyte', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(177900, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0141795', 'abnormal glycosylation', 0.4782608695652174, 4.758907843651163, 1.508641575552437, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(177901, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0131694', 'abnormal RNA polymerase II activity', 0.4583333333333333, 4.758907843651163, 1.4768771428276568, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(177902, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0100084', 'abnormal anatomical group', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(177903, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0101110', 'abnormal cell-free extract', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(177904, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0128000', 'absent behavior', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(177905, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0131667', 'abnormal actin cytoskeleton', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(177906, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0131666', 'abnormal adherens junction', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(177907, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0141266', 'abnormal surface breathing', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(177908, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0131675', 'abnormal spindle microtubule', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(177909, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0101141', 'abnormal Keller explant', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(177910, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0100515', 'abnormal somatic stem cell', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(177911, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0141880', 'abnormal ethanolamine metabolic process', 0.44, 4.758907843651163, 1.447038165082909, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(177912, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0100232', 'abnormal lymphatic system', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(177913, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0133388', 'absent insulin receptor signaling pathway', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(177914, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0115505', 'dead whole organism', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(177915, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0100337', 'abnormal zygote', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(177916, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0141884', 'abnormal phosphagen metabolic process', 0.4230769230769231, 4.758907843651163, 1.418937661667548, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(177917, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0115512', 'abnormally semi-erect whole organism', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(177918, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0100599', 'abnormal adult immune system', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(177919, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0101409', 'abnormal perivitelline space', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(177920, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0101513', 'abnormal basal body', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(177921, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0101468', 'abnormal stage I oocyte', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(177922, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0107259', 'abnormal animal-vegetal axis', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(177923, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0101535', 'abnormal absorptive cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(177924, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0141789', 'abnormal hormone catabolic process', 0.44, 4.758907843651163, 1.447038165082909, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(177925, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0101498', 'abnormal stage II oocyte', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(177926, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0141315', 'abnormal anatomical region', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(177927, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0141892', 'abnormal inositol metabolic process', 0.4782608695652174, 4.758907843651163, 1.508641575552437, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(177928, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0100176', 'abnormal stage VI oocyte', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(177929, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0101480', 'abnormal stage V oocyte', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(177930, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0100377', 'abnormal connective tissue', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(177931, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0100274', 'abnormal sensory system', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(177932, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0141883', 'abnormal glycerol metabolic process', 0.4230769230769231, 4.758907843651163, 1.418937661667548, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(177933, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0101071', 'abnormal endoplasmic reticulum', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(177934, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0100026', 'abnormal germ cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(177935, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0107260', 'abnormal anterior-posterior axis', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(177936, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0100437', 'abnormal proepicardium', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(177937, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0131677', 'abnormal actin filament', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(177938, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0131469', 'abnormal heart process', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(177939, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0131730', 'abnormal regulation of protein folding', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(177940, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0101220', 'abnormal centriole', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(177941, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0100653', 'abnormal myoblast', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(177942, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0100573', 'abnormal extraembryonic structure', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(177943, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0141860', 'abnormal malate-aspartate shuttle', 0.5, 4.758907843651163, 1.5425478669479211, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(177944, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0141859', 'abnormal lactose catabolic process', 0.4230769230769231, 4.758907843651163, 1.418937661667548, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(177945, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0100969', 'abnormal disaggregated/reaggregated ectoderm treated with activin', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(177946, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0100674', 'abnormal secondary oogonium', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(177947, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0141852', 'abnormal glucose metabolic process', 0.4230769230769231, 4.758907843651163, 1.418937661667548, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(177948, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0100285', 'abnormal progenitor cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(177949, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0141777', 'abnormal catabolic process', 0.5238095238095238, 4.758907843651163, 1.5788480773767701, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(177950, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0141781', 'abnormal secondary metabolic process', 0.5238095238095238, 4.758907843651163, 1.5788480773767701, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(177951, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0100386', 'abnormal limb', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(177952, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0101061', 'abnormal plasma membrane', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(177953, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0141770', 'abnormal urate homeostasis', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(177954, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0100976', 'abnormal multiciliated cell', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(177955, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0141263', 'abnormal visually guided collision avoidance behavior', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(177956, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0100956', 'abnormal centrosome', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(177957, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0116494', 'absent biological process', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(177958, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0141809', 'abnormal catalytic activity', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(177959, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0141276', 'decreased surface breathing', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(177960, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0141898', 'abnormal maltose metabolic process', 0.4583333333333333, 4.758907843651163, 1.4768771428276568, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(177961, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0100423', 'abnormal process', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(177962, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0100902', 'abnormal spermatocyte', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(177963, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:00000000', 'Xenopus phenotype', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(177964, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0141772', 'abnormal water homeostasis', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(177965, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0141745', 'abnormal creatinine homeostasis', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(177966, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0141904', 'abnormal glucosamine metabolic process', 0.5238095238095238, 4.758907843651163, 1.5788480773767701, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(177967, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0100852', 'abnormal interdigital region', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(177968, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0101366', 'abnormal morula cell', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(177969, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0100032', 'abnormal nervous system', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(177970, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0100025', 'abnormal oocyte', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(177971, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0100899', 'abnormal secondary spermatogonium', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(177972, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0141782', 'abnormal methylation', 0.5238095238095238, 4.758907843651163, 1.5788480773767701, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(177973, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0107270', 'abnormal proximal-distal axis', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(177974, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0100585', 'abnormal elastica externa', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(177975, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0100533', 'abnormal melanoblast', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(177976, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0141264', 'abnormal schooling behavior', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(177977, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0101004', 'abnormal acid secreting cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(177978, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0107284', 'abnormal migrating myoblast', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(177979, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0141767', 'abnormal temperature homeostasis', 0.44, 4.758907843651163, 1.447038165082909, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(177980, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0141499', 'abnormal tadpole', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(177981, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0141850', 'abnormal galactose metabolic process', 0.4230769230769231, 4.758907843651163, 1.418937661667548, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(177982, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0131729', 'abnormal regulation of growth rate', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(177983, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0141881', 'abnormal fructose metabolic process', 0.4230769230769231, 4.758907843651163, 1.418937661667548, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(177984, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0100691', 'abnormal keratin accumulating cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(177985, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0141864', 'abnormal 5-methylcytosine metabolic process', 0.4230769230769231, 4.758907843651163, 1.418937661667548, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(177986, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0141771', 'abnormal urea homeostasis', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(177987, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0131745', 'abnormal axis elongation', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(177988, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0100728', 'abnormal cell condensation', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(177989, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0141854', 'abnormal glutathione metabolic process', 0.4230769230769231, 4.758907843651163, 1.418937661667548, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(177990, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0141900', 'abnormal mannose metabolic process', 0.4230769230769231, 4.758907843651163, 1.418937661667548, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(177991, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0116434', 'abnormal biological process', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(177992, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0100081', 'abnormal anatomical entity in vitro', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(177993, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0101472', 'abnormal zygote cortex', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(177994, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0100010', 'abnormal multicellular anatomical structure', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(177995, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0141791', 'abnormal primary metabolic process', 0.5238095238095238, 4.758907843651163, 1.5788480773767701, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(177996, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0142057', 'abnormal desmosome', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(177997, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0115509', 'abnormally semi-viable whole organism', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(177998, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0141778', 'abnormal biosynthetic process', 0.5238095238095238, 4.758907843651163, 1.5788480773767701, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(177999, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0101264', 'abnormal mitotic spindle', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(178000, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0100638', 'abnormal polar body', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(178001, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0141911', 'abnormal ribose phosphate metabolic process', 0.4583333333333333, 4.758907843651163, 1.4768771428276568, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(178002, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0101448', 'abnormal myelin accumulating cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(178003, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0141908', 'abnormal pyridine metabolic process', 0.4230769230769231, 4.758907843651163, 1.418937661667548, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(178004, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0100574', 'abnormal gastrula cell', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(178005, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0141910', 'abnormal D-ribose metabolic process', 0.4230769230769231, 4.758907843651163, 1.418937661667548, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(178006, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0141784', 'abnormal cellular hormone metabolic process', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(178007, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0100392', 'abnormal cilium', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(178008, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0100004', 'abnormal cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(178009, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0141743', 'abnormal chemical homeostasis within a tissue', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(178010, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0141903', 'abnormal inositol phosphate metabolic process', 0.4230769230769231, 4.758907843651163, 1.418937661667548, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(178011, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0101237', 'abnormal mucus secreting cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(178012, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0100546', 'abnormal whole organism', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(178013, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0100307', 'abnormal blastomere', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(178014, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0101435', 'abnormal paracrine cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(178015, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0141792', 'abnormal small molecule metabolic process', 0.5238095238095238, 4.758907843651163, 1.5788480773767701, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(178016, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0100289', 'abnormal chondroblast', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(178017, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0100429', 'abnormal spermatid', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(178018, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0100239', 'abnormal acellular anatomical structure', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(178019, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0131685', 'abnormal cortical actin cytoskeleton', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(178020, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0101157', 'abnormal female organism', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(178021, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0141797', 'abnormal hydrogen metabolic process', 0.5238095238095238, 4.758907843651163, 1.5788480773767701, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(178022, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0141600', 'absent metamorphosis', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(178023, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0141796', 'abnormal demethylation', 0.5238095238095238, 4.758907843651163, 1.5788480773767701, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(178024, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0131725', 'abnormal phosphorylation of RNA polymerase II C-terminal domain', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(178025, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0141907', 'abnormal putrescine metabolic process', 0.4782608695652174, 4.758907843651163, 1.508641575552437, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(178026, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0100721', 'abnormal centromere', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(178027, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0100108', 'abnormal cell part', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(178028, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0141265', 'abnormal escape behavior', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(178029, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0141794', 'abnormal prosthetic group metabolic process', 0.5238095238095238, 4.758907843651163, 1.5788480773767701, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(178030, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0100344', 'abnormal portion of organism substance', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(178031, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0100258', 'abnormal organ part', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(178032, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0100754', 'abnormal electrically active cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(178033, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0100006', 'abnormal anatomical structure', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(178034, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0141783', 'abnormal collagen metabolic process', 0.5238095238095238, 4.758907843651163, 1.5788480773767701, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(178035, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0141872', 'abnormal cholesterol metabolic process', 0.4074074074074074, 4.758907843651163, 1.392413123563799, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(178036, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0100894', 'abnormal nucleus', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(178037, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0141272', 'absent surface breathing', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(178038, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0100791', 'abnormal multiciliated cell precursor', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(178039, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0100545', 'abnormal male organism', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(178040, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0141786', 'abnormal pigment metabolic process', 0.5238095238095238, 4.758907843651163, 1.5788480773767701, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(178041, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0141877', 'abnormal 2-deoxyribose 1-phosphate metabolic process', 0.4583333333333333, 4.758907843651163, 1.4768771428276568, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(178042, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0101461', 'abnormal sperm entry point', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(178043, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0100172', 'abnormal stem cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(178044, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0100372', 'abnormal hematological system', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(178045, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0101240', 'abnormal ciliated non-epidermal cell', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(178046, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0141787', 'abnormal hormone metabolic process', 0.5238095238095238, 4.758907843651163, 1.5788480773767701, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(178047, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0141866', 'abnormal dicarboxylic acid metabolic process', 0.4074074074074074, 4.758907843651163, 1.392413123563799, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(178048, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0100581', 'abnormal immune system', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(178049, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0100501', 'abnormal urogenital system', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(178050, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0141798', 'abnormal lipid metabolic process', 0.4782608695652174, 4.758907843651163, 1.508641575552437, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(178051, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0131723', 'abnormal pathway-restricted SMAD protein phosphorylation', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(178052, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0101113', 'abnormal stage IV oocyte', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(178053, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0115508', 'abnormally peramorphic growth of whole organism', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(178054, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0100907', 'abnormal cytoplasm', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(178055, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0101297', 'abnormal barrier cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(178056, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0100317', 'abnormal respiratory system', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(178057, 'HP:0003643', 'Sulfite oxidase deficiency', 'XPO:0100308', 'abnormal early embryonic cell', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(178058, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100674', 'abnormal secondary oogonium', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(178059, 'HP:0030366', 'Delivery by Odon device', 'XPO:0101498', 'abnormal stage II oocyte', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(178060, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100308', 'abnormal early embryonic cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(178061, 'HP:0030366', 'Delivery by Odon device', 'XPO:0101547', 'abnormal lampbrush chromosome', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(178062, 'HP:0030366', 'Delivery by Odon device', 'XPO:0116494', 'absent biological process', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(178063, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100025', 'abnormal oocyte', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(178064, 'HP:0030366', 'Delivery by Odon device', 'XPO:0141792', 'abnormal small molecule metabolic process', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(178065, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100402', 'abnormal zeugopod', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(178066, 'HP:0030366', 'Delivery by Odon device', 'XPO:0107265', 'abnormal posterior side', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178067, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100781', 'abnormal presumptive ectoderm', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178068, 'HP:0030366', 'Delivery by Odon device', 'XPO:0101424', 'abnormal coelomic epithelium', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178069, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100549', 'abnormal mitotic cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(178070, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100956', 'abnormal centrosome', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(178071, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100285', 'abnormal progenitor cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(178072, 'HP:0030366', 'Delivery by Odon device', 'XPO:0101713', 'abnormal anatomical entity in vitro morphology', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178073, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100108', 'abnormal cell part', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(178074, 'HP:0030366', 'Delivery by Odon device', 'XPO:0141784', 'abnormal cellular hormone metabolic process', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(178075, 'HP:0030366', 'Delivery by Odon device', 'XPO:0101040', 'abnormal axial mesoderm', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178076, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100317', 'abnormal respiratory system', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(178077, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100032', 'abnormal nervous system', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(178078, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100493', 'abnormal liver and biliary system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(178079, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100545', 'abnormal male organism', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178080, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100688', 'abnormal adipose tissue', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(178081, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100574', 'abnormal gastrula cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(178082, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100573', 'abnormal extraembryonic structure', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178083, 'HP:0030366', 'Delivery by Odon device', 'XPO:0141786', 'abnormal pigment metabolic process', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(178084, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100640', 'abnormal notochordal sheath', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(178085, 'HP:0030366', 'Delivery by Odon device', 'XPO:0101241', 'abnormal nucleate erythrocyte', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(178086, 'HP:0030366', 'Delivery by Odon device', 'XPO:0141782', 'abnormal methylation', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(178087, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100854', 'abnormal spiracle', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178088, 'HP:0030366', 'Delivery by Odon device', 'XPO:0107269', 'abnormal right side', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178089, 'HP:0030366', 'Delivery by Odon device', 'XPO:0141267', 'abnormal resting posture', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(178090, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100581', 'abnormal immune system', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(178091, 'HP:0030366', 'Delivery by Odon device', 'XPO:0107262', 'abnormal left-right axis', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178092, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100258', 'abnormal organ part', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178093, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100800', 'abnormal ventral marginal zone', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178094, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100742', 'abnormal musculoskeletal system', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178095, 'HP:0030366', 'Delivery by Odon device', 'XPO:0101141', 'abnormal Keller explant', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178096, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100416', 'abnormal ligament', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(178097, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100667', 'abnormal vegetal yolk mass', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178098, 'HP:0030366', 'Delivery by Odon device', 'XPO:0131669', 'abnormal Roux spot', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(178099, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100976', 'abnormal multiciliated cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(178100, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100295', 'abnormal extracellular matrix', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178101, 'HP:0030366', 'Delivery by Odon device', 'XPO:0101333', 'abnormal barrier epithelial cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(178102, 'HP:0030366', 'Delivery by Odon device', 'XPO:0131666', 'abnormal adherens junction', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(178103, 'HP:0030366', 'Delivery by Odon device', 'XPO:0101110', 'abnormal cell-free extract', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178104, 'HP:0030366', 'Delivery by Odon device', 'XPO:0141775', 'abnormal nitrogen compound metabolic process', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(178105, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100009', 'abnormal multi-tissue structure', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178106, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100665', 'abnormal egg jelly', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178107, 'HP:0030366', 'Delivery by Odon device', 'XPO:0131677', 'abnormal actin filament', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(178108, 'HP:0030366', 'Delivery by Odon device', 'XPO:0101092', 'abnormal dorso-lateral marginal zone', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178109, 'HP:0030366', 'Delivery by Odon device', 'XPO:0115512', 'abnormally semi-erect whole organism', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178110, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100203', 'abnormal endocrine cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(178111, 'HP:0030366', 'Delivery by Odon device', 'XPO:0107276', 'abnormal dorsal region', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178112, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100842', 'abnormal left-dorsal blastomere', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(178113, 'HP:0030366', 'Delivery by Odon device', 'XPO:0101406', 'abnormal cleavage furrow', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178114, 'HP:0030366', 'Delivery by Odon device', 'XPO:0107263', 'abnormal anatomical side', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178115, 'HP:0030366', 'Delivery by Odon device', 'XPO:0141497', 'abnormal lymphoblast', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(178116, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100120', 'abnormal genital system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(178117, 'HP:0030366', 'Delivery by Odon device', 'XPO:0141797', 'abnormal hydrogen metabolic process', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(178118, 'HP:0030366', 'Delivery by Odon device', 'XPO:0141263', 'abnormal visually guided collision avoidance behavior', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(178119, 'HP:0030366', 'Delivery by Odon device', 'XPO:0101264', 'abnormal mitotic spindle', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(178120, 'HP:0030366', 'Delivery by Odon device', 'XPO:0101157', 'abnormal female organism', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178121, 'HP:0030366', 'Delivery by Odon device', 'XPO:0107312', 'abnormal filopodium', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(178122, 'HP:0030366', 'Delivery by Odon device', 'XPO:0101463', 'abnormal right-ventral blastomere', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(178123, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100437', 'abnormal proepicardium', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(178124, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100991', 'abnormal iliac process primordium', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178125, 'HP:0030366', 'Delivery by Odon device', 'XPO:0101389', 'abnormal wedge region', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(178126, 'HP:0030366', 'Delivery by Odon device', 'XPO:0107267', 'abnormal ventral side', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178127, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100339', 'abnormal circumblastoporal collar', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178128, 'HP:0030366', 'Delivery by Odon device', 'XPO:0107272', 'abnormal axial region', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178129, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100386', 'abnormal limb', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(178130, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100423', 'abnormal process', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178131, 'HP:0030366', 'Delivery by Odon device', 'XPO:0101098', 'abnormal mineralized extracellular matrix', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178132, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100415', 'abnormal secretory epithelial cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(178133, 'HP:0030366', 'Delivery by Odon device', 'XPO:0101004', 'abnormal acid secreting cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(178134, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100378', 'abnormal perichondrium', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(178135, 'HP:0030366', 'Delivery by Odon device', 'XPO:0141264', 'abnormal schooling behavior', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(178136, 'HP:0030366', 'Delivery by Odon device', 'XPO:0141743', 'abnormal chemical homeostasis within a tissue', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(178137, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100383', 'abnormal amputated fin', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178138, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100786', 'abnormal presumptive axial mesoderm', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178139, 'HP:0030366', 'Delivery by Odon device', 'XPO:0101347', 'abnormal hindlimb region', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178140, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100196', 'abnormal neuron', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(178141, 'HP:0030366', 'Delivery by Odon device', 'XPO:0101297', 'abnormal barrier cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(178142, 'HP:0030366', 'Delivery by Odon device', 'XPO:0101448', 'abnormal myelin accumulating cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(178143, 'HP:0030366', 'Delivery by Odon device', 'XPO:0101220', 'abnormal centriole', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(178144, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100888', 'abnormal microtubule', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(178145, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100152', 'abnormal alimentary system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(178146, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100724', 'abnormal kinetochore', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(178147, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100707', 'abnormal central vegetal yolk mass', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178148, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100846', 'abnormal hindlimb', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(178149, 'HP:0030366', 'Delivery by Odon device', 'XPO:0101570', 'abnormal forelimb region', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178150, 'HP:0030366', 'Delivery by Odon device', 'XPO:0141860', 'abnormal malate-aspartate shuttle', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(178151, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100004', 'abnormal cell', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(178152, 'HP:0030366', 'Delivery by Odon device', 'XPO:0101010', 'abnormal dorsal marginal zone', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178153, 'HP:0030366', 'Delivery by Odon device', 'XPO:0101575', 'abnormal vitelline membrane', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(178154, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100201', 'abnormal cavitated compound organ', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178155, 'HP:0030366', 'Delivery by Odon device', 'XPO:0107253', 'abnormal enteric nervous system', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(178156, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100394', 'abnormal marginal zone', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178157, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100392', 'abnormal cilium', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(178158, 'HP:0030366', 'Delivery by Odon device', 'XPO:0101237', 'abnormal mucus secreting cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(178159, 'HP:0030366', 'Delivery by Odon device', 'XPO:0101976', 'abnormal portion of organism substance morphology', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178160, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100084', 'abnormal anatomical group', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178161, 'HP:0030366', 'Delivery by Odon device', 'XPO:0141778', 'abnormal biosynthetic process', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(178162, 'HP:0030366', 'Delivery by Odon device', 'XPO:0101029', 'abnormal right spleen primordium', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(178163, 'HP:0030366', 'Delivery by Odon device', 'XPO:0107271', 'abnormal apical region', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178164, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100232', 'abnormal lymphatic system', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(178165, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100026', 'abnormal germ cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(178166, 'HP:0030366', 'Delivery by Odon device', 'XPO:0101132', 'abnormal apoptotic cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(178167, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100023', 'abnormal mesenchyme', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178168, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100784', 'abnormal left blastomere', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(178169, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100060', 'abnormal regenerating tissue', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178170, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100653', 'abnormal myoblast', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(178171, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100081', 'abnormal anatomical entity in vitro', 0.5294117647058824, 1.706362323152461, 0.9504568842024205, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178172, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100225', 'abnormal endocrine system', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(178173, 'HP:0030366', 'Delivery by Odon device', 'XPO:0101513', 'abnormal basal body', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(178174, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100912', 'abnormal trabecula', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178175, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100900', 'abnormal angioblast', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(178176, 'HP:0030366', 'Delivery by Odon device', 'XPO:0141841', 'abnormality of whole organism mass', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(178177, 'HP:0030366', 'Delivery by Odon device', 'XPO:0141718', 'abnormal posterior notochord', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(178178, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100482', 'abnormal Mullerian duct', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(178179, 'HP:0030366', 'Delivery by Odon device', 'XPO:0107264', 'abnormal anterior side', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178180, 'HP:0030366', 'Delivery by Odon device', 'XPO:0101468', 'abnormal stage I oocyte', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(178181, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100274', 'abnormal sensory system', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(178182, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100754', 'abnormal electrically active cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(178183, 'HP:0030366', 'Delivery by Odon device', 'XPO:0107285', 'abnormal flexural organ', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(178184, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100104', 'abnormal embryonic structure', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178185, 'HP:0030366', 'Delivery by Odon device', 'XPO:0141748', 'abnormal gas homeostasis', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(178186, 'HP:0030366', 'Delivery by Odon device', 'XPO:0141714', 'abnormal anterior notochord', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(178187, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100605', 'abnormal prechordal plate', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178188, 'HP:0030366', 'Delivery by Odon device', 'XPO:0142056', 'abnormal main body axis', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178189, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100728', 'abnormal cell condensation', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178190, 'HP:0030366', 'Delivery by Odon device', 'XPO:0101503', 'abnormal organ cortex', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178191, 'HP:0030366', 'Delivery by Odon device', 'XPO:0101240', 'abnormal ciliated non-epidermal cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(178192, 'HP:0030366', 'Delivery by Odon device', 'XPO:0115505', 'dead whole organism', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178193, 'HP:0030366', 'Delivery by Odon device', 'XPO:0101405', 'abnormal ring structure', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(178194, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100028', 'abnormal anatomical cluster', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178195, 'HP:0030366', 'Delivery by Odon device', 'XPO:0101378', 'abnormal blastomere D1', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(178196, 'HP:0030366', 'Delivery by Odon device', 'XPO:0101228', 'abnormal mesenchymal stem cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(178197, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100239', 'abnormal acellular anatomical structure', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178198, 'HP:0030366', 'Delivery by Odon device', 'XPO:0101480', 'abnormal stage V oocyte', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(178199, 'HP:0030366', 'Delivery by Odon device', 'XPO:0141776', 'abnormal metabolic process', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(178200, 'HP:0030366', 'Delivery by Odon device', 'XPO:0101409', 'abnormal perivitelline space', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(178201, 'HP:0030366', 'Delivery by Odon device', 'XPO:0142057', 'abnormal desmosome', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(178202, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100858', 'abnormal presumptive midbrain-hindbrain boundary', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(178203, 'HP:0030366', 'Delivery by Odon device', 'XPO:0131725', 'abnormal phosphorylation of RNA polymerase II C-terminal domain', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(178204, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100546', 'abnormal whole organism', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178205, 'HP:0030366', 'Delivery by Odon device', 'XPO:0141265', 'abnormal escape behavior', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(178206, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100721', 'abnormal centromere', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(178207, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100587', 'abnormal vestibuloauditory system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(178208, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100796', 'abnormal pseudoblastema', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178209, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100969', 'abnormal disaggregated/reaggregated ectoderm treated with activin', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178210, 'HP:0030366', 'Delivery by Odon device', 'XPO:0115758', 'abnormally decreased mobility of melanoblast', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(178211, 'HP:0030366', 'Delivery by Odon device', 'XPO:0141787', 'abnormal hormone metabolic process', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(178212, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100172', 'abnormal stem cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(178213, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100547', 'abnormal blastomere V2', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(178214, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100477', 'abnormal pericyte', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(178215, 'HP:0030366', 'Delivery by Odon device', 'XPO:0141276', 'decreased surface breathing', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(178216, 'HP:0030366', 'Delivery by Odon device', 'XPO:0141315', 'abnormal anatomical region', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178217, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100205', 'abnormal limb segment', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(178218, 'HP:0030366', 'Delivery by Odon device', 'XPO:0101168', 'abnormal circulating cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(178219, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100913', 'abnormal Brachets cleft', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178220, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100164', 'abnormal neural nucleus', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(178221, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100722', 'abnormal barbel', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178222, 'HP:0030366', 'Delivery by Odon device', 'XPO:0102113', 'abnormal anatomical line morphology', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178223, 'HP:0030366', 'Delivery by Odon device', 'XPO:0101587', 'abnormal hemangioblast', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(178224, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100557', 'abnormal prime meridian', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178225, 'HP:0030366', 'Delivery by Odon device', 'XPO:0101149', 'abnormal amputated limb', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178226, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100070', 'abnormal anatomical system', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178227, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100553', 'abnormal laryngeal muscle primordium', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178228, 'HP:0030366', 'Delivery by Odon device', 'XPO:0101074', 'abnormal germinal vesicle', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(178229, 'HP:0030366', 'Delivery by Odon device', 'XPO:0101569', 'abnormal activin-induced ectoderm', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178230, 'HP:0030366', 'Delivery by Odon device', 'XPO:0131687', 'abnormal astral microtubule', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(178231, 'HP:0030366', 'Delivery by Odon device', 'XPO:0101221', 'abnormal larval immune system', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(178232, 'HP:0030366', 'Delivery by Odon device', 'XPO:0141791', 'abnormal primary metabolic process', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(178233, 'HP:0030366', 'Delivery by Odon device', 'XPO:0101519', 'abnormal hypobranchial placode', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178234, 'HP:0030366', 'Delivery by Odon device', 'XPO:0101061', 'abnormal plasma membrane', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(178235, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100429', 'abnormal spermatid', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(178236, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100894', 'abnormal nucleus', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(178237, 'HP:0030366', 'Delivery by Odon device', 'XPO:0141266', 'abnormal surface breathing', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(178238, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100890', 'abnormal pharyngeal cavity', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(178239, 'HP:0030366', 'Delivery by Odon device', 'XPO:0141499', 'abnormal tadpole', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178240, 'HP:0030366', 'Delivery by Odon device', 'XPO:0141783', 'abnormal collagen metabolic process', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(178241, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100902', 'abnormal spermatocyte', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(178242, 'HP:0030366', 'Delivery by Odon device', 'XPO:0101107', 'abnormal erythroid cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(178243, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100289', 'abnormal chondroblast', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(178244, 'HP:0030366', 'Delivery by Odon device', 'XPO:0101450', 'abnormal myeloid cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(178245, 'HP:0030366', 'Delivery by Odon device', 'XPO:0107259', 'abnormal animal-vegetal axis', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178246, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100427', 'abnormal olfactory system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(178247, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100484', 'abnormal cement gland primordium', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178248, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100277', 'abnormal blastocoel', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178249, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100449', 'abnormal lymphocyte', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(178250, 'HP:0030366', 'Delivery by Odon device', 'XPO:0101302', 'abnormal subcortical cytoplasm', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(178251, 'HP:0030366', 'Delivery by Odon device', 'XPO:0101311', 'abnormal bottle cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(178252, 'HP:0030366', 'Delivery by Odon device', 'XPO:0141772', 'abnormal water homeostasis', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(178253, 'HP:0030366', 'Delivery by Odon device', 'XPO:0141715', 'abnormal septum', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178254, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100344', 'abnormal portion of organism substance', 0.5294117647058824, 1.706362323152461, 0.9504568842024205, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178255, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100422', 'abnormal notochord', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(178256, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100515', 'abnormal somatic stem cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(178257, 'HP:0030366', 'Delivery by Odon device', 'XPO:0107268', 'abnormal left side', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178258, 'HP:0030366', 'Delivery by Odon device', 'XPO:0101435', 'abnormal paracrine cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(178259, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100218', 'abnormal epithelial cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(178260, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100003', 'abnormal organism subdivision', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178261, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100823', 'abnormal blood', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(178262, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100363', 'abnormal cardiovascular system', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178263, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100917', 'abnormal stage III oocyte', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(178264, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100531', 'abnormal proliferative region', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178265, 'HP:0030366', 'Delivery by Odon device', 'XPO:0141790', 'abnormal cellular metabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(178266, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100610', 'abnormal appendage', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178267, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100103', 'abnormal trunk', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178268, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100856', 'abnormal simple organ', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178269, 'HP:0030366', 'Delivery by Odon device', 'XPO:0101109', 'abnormal egg cell-free extract', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178270, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100186', 'abnormal uveal tract', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178271, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100642', 'abnormal gustatory system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(178272, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100377', 'abnormal connective tissue', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(178273, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100231', 'abnormal compound organ', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178274, 'HP:0030366', 'Delivery by Odon device', 'XPO:0101174', 'abnormal articular system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(178275, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100031', 'abnormal central nervous system', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(178276, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100207', 'abnormal blastema', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178277, 'HP:0030366', 'Delivery by Odon device', 'XPO:0101451', 'abnormal dorsal lymph space', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(178278, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100069', 'abnormal urinary system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(178279, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100585', 'abnormal elastica externa', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(178280, 'HP:0030366', 'Delivery by Odon device', 'XPO:0101553', 'abnormal dental epithelium', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178281, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100465', 'abnormal skeletal system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(178282, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100503', 'abnormal blastomere D2', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(178283, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100501', 'abnormal urogenital system', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(178284, 'HP:0030366', 'Delivery by Odon device', 'XPO:0101461', 'abnormal sperm entry point', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(178285, 'HP:0030366', 'Delivery by Odon device', 'XPO:0141794', 'abnormal prosthetic group metabolic process', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(178286, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100468', 'abnormal muscular system', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178287, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100249', 'abnormal avascular GAG-rich matrix', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178288, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100852', 'abnormal interdigital region', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(178289, 'HP:0030366', 'Delivery by Odon device', 'XPO:0141904', 'abnormal glucosamine metabolic process', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(178290, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100417', 'abnormal dense regular connective tissue', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(178291, 'HP:0030366', 'Delivery by Odon device', 'XPO:0101543', 'abnormal external gill', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(178292, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100384', 'abnormal amputated tissue', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178293, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100807', 'abnormal matrix-based tissue', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178294, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100533', 'abnormal melanoblast', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(178295, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100511', 'abnormal stylopod', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(178296, 'HP:0030366', 'Delivery by Odon device', 'XPO:0142054', 'abnormal digestive tract', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(178297, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100899', 'abnormal secondary spermatogonium', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(178298, 'HP:0030366', 'Delivery by Odon device', 'XPO:0101638', 'abnormal anatomical structure morphology', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178299, 'HP:0030366', 'Delivery by Odon device', 'XPO:0141745', 'abnormal creatinine homeostasis', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(178300, 'HP:0030366', 'Delivery by Odon device', 'XPO:0131723', 'abnormal pathway-restricted SMAD protein phosphorylation', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(178301, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100827', 'abnormal atypical epithelium', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178302, 'HP:0030366', 'Delivery by Odon device', 'XPO:0107266', 'abnormal dorsal side', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178303, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100192', 'abnormal epithelium', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178304, 'HP:0030366', 'Delivery by Odon device', 'XPO:0131691', 'abnormal molecular function', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(178305, 'HP:0030366', 'Delivery by Odon device', 'XPO:0116434', 'abnormal biological process', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(178306, 'HP:0030366', 'Delivery by Odon device', 'XPO:0141271', 'increased surface breathing', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(178307, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100273', 'abnormal visual system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(178308, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100151', 'abnormal primordium', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178309, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100282', 'abnormal pelvic girdle primordium', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178310, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100158', 'abnormal neuromere', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(178311, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100135', 'abnormal surface structure', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178312, 'HP:0030366', 'Delivery by Odon device', 'XPO:0101366', 'abnormal morula cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(178313, 'HP:0030366', 'Delivery by Odon device', 'XPO:00000000', 'Xenopus phenotype', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(178314, 'HP:0030366', 'Delivery by Odon device', 'XPO:0107273', 'abnormal basal region', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178315, 'HP:0030366', 'Delivery by Odon device', 'XPO:0141738', 'abnormal carbon dioxide homeostasis', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(178316, 'HP:0030366', 'Delivery by Odon device', 'XPO:0101573', 'abnormal peripheral vegetal yolk mass', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178317, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100509', 'abnormal germ plasm', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(178318, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100293', 'abnormal duct', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178319, 'HP:0030366', 'Delivery by Odon device', 'XPO:0107258', 'abnormal anatomical axis', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178320, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100802', 'abnormal exocrine cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(178321, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100268', 'abnormal circulatory system', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178322, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100062', 'abnormal anatomical space', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178323, 'HP:0030366', 'Delivery by Odon device', 'XPO:0101212', 'abnormal glomeral mesenchyme', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(178324, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100114', 'abnormal peripheral nervous system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(178325, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100175', 'abnormal migrating neuroblast', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(178326, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100261', 'abnormal multilaminar epithelium', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178327, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100702', 'abnormal glial cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(178328, 'HP:0030366', 'Delivery by Odon device', 'XPO:0101326', 'abnormal cementoblast', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(178329, 'HP:0030366', 'Delivery by Odon device', 'XPO:0101497', 'abnormal ciliary axoneme', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(178330, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100162', 'abnormal presumptive rhombomere', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178331, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100915', 'abnormal dermal system', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178332, 'HP:0030366', 'Delivery by Odon device', 'XPO:0101200', 'abnormal joint region', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178333, 'HP:0030366', 'Delivery by Odon device', 'XPO:0101176', 'abnormal non-ciliated epithelial cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(178334, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100791', 'abnormal multiciliated cell precursor', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(178335, 'HP:0030366', 'Delivery by Odon device', 'XPO:0101136', 'abnormal ooplasm', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(178336, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100868', 'abnormal transporting epithelium', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178337, 'HP:0030366', 'Delivery by Odon device', 'XPO:0101099', 'abnormal ventro-lateral marginal zone', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178338, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100014', 'abnormal tissue', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178339, 'HP:0030366', 'Delivery by Odon device', 'XPO:0131675', 'abnormal spindle microtubule', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(178340, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100481', 'abnormal anatomical line', 0.5294117647058824, 1.706362323152461, 0.9504568842024205, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178341, 'HP:0030366', 'Delivery by Odon device', 'XPO:0141272', 'absent surface breathing', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(178342, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100715', 'abnormal ciliated cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(178343, 'HP:0030366', 'Delivery by Odon device', 'XPO:0141796', 'abnormal demethylation', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(178344, 'HP:0030366', 'Delivery by Odon device', 'XPO:0115508', 'abnormally peramorphic growth of whole organism', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178345, 'HP:0030366', 'Delivery by Odon device', 'XPO:0101096', 'abnormal tendon', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(178346, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100133', 'abnormal solid compound organ', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178347, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100999', 'abnormal serous membrane', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178348, 'HP:0030366', 'Delivery by Odon device', 'XPO:0107260', 'abnormal anterior-posterior axis', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178349, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100704', 'abnormal Merkel cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(178350, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100862', 'abnormal blastomere V1', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(178351, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100251', 'abnormal proteinaceous extracellular matrix', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178352, 'HP:0030366', 'Delivery by Odon device', 'XPO:0101224', 'abnormal dorsal involuting marginal zone', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178353, 'HP:0030366', 'Delivery by Odon device', 'XPO:0141771', 'abnormal urea homeostasis', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(178354, 'HP:0030366', 'Delivery by Odon device', 'XPO:0141781', 'abnormal secondary metabolic process', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(178355, 'HP:0030366', 'Delivery by Odon device', 'XPO:0115509', 'abnormally semi-viable whole organism', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178356, 'HP:0030366', 'Delivery by Odon device', 'XPO:0101072', 'abnormal mitochondrial cloud', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(178357, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100599', 'abnormal adult immune system', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(178358, 'HP:0030366', 'Delivery by Odon device', 'XPO:0115391', 'abnormally undifferentiated alimentary system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(178359, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100887', 'abnormal right-dorsal blastomere', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(178360, 'HP:0030366', 'Delivery by Odon device', 'XPO:0101362', 'abnormal vegetal cortex', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(178361, 'HP:0030366', 'Delivery by Odon device', 'XPO:0101501', 'abnormal parabrachial area', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(178362, 'HP:0030366', 'Delivery by Odon device', 'XPO:0142052', 'abnormal nasal region', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(178363, 'HP:0030366', 'Delivery by Odon device', 'XPO:0107261', 'abnormal dorsal-ventral axis', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178364, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100907', 'abnormal cytoplasm', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(178365, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100458', 'abnormal autopod', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(178366, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100935', 'abnormal skeleton', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(178367, 'HP:0030366', 'Delivery by Odon device', 'XPO:0107288', 'abnormal larval alimentary system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(178368, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100989', 'abnormal right blastomere', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(178369, 'HP:0030366', 'Delivery by Odon device', 'XPO:0101078', 'abnormal mucous gland', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178370, 'HP:0030366', 'Delivery by Odon device', 'XPO:0107278', 'abnormal medial region', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178371, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100537', 'abnormal medium cavity', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(178372, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100638', 'abnormal polar body', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(178373, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100843', 'abnormal fasciculated network of fibrils', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(178374, 'HP:0030366', 'Delivery by Odon device', 'XPO:0101023', 'abnormal ultimobranchial body', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(178375, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100403', 'abnormal forelimb', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(178376, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100626', 'abnormal primordial germ cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(178377, 'HP:0030366', 'Delivery by Odon device', 'XPO:0101467', 'abnormal alkali secreting cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(178378, 'HP:0030366', 'Delivery by Odon device', 'XPO:0101113', 'abnormal stage IV oocyte', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(178379, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100265', 'abnormal sensory epithelial cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(178380, 'HP:0030366', 'Delivery by Odon device', 'XPO:0141770', 'abnormal urate homeostasis', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(178381, 'HP:0030366', 'Delivery by Odon device', 'XPO:0101411', 'abnormal marginal zone (sensu neural)', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178382, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100202', 'abnormal embryo', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178383, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100010', 'abnormal multicellular anatomical structure', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178384, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100337', 'abnormal zygote', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(178385, 'HP:0030366', 'Delivery by Odon device', 'XPO:0107311', 'abnormal apical junction complex', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(178386, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100588', 'abnormal unicellular gland', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178387, 'HP:0030366', 'Delivery by Odon device', 'XPO:0101283', 'abnormal left-ventral blastomere', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(178388, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100762', 'abnormal intersomitic region', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178389, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100307', 'abnormal blastomere', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(178390, 'HP:0030366', 'Delivery by Odon device', 'XPO:0101349', 'abnormal trunk region', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178391, 'HP:0030366', 'Delivery by Odon device', 'XPO:0142051', 'abnormal cerebrospinal fluid', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(178392, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100691', 'abnormal keratin accumulating cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(178393, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100612', 'abnormal unilaminar epithelium', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178394, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100067', 'abnormal animal hemisphere', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178395, 'HP:0030366', 'Delivery by Odon device', 'XPO:0131685', 'abnormal cortical actin cytoskeleton', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(178396, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100256', 'abnormal paired appendage', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178397, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100816', 'abnormal blastocoel anlage', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178398, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100296', 'abnormal tail region', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178399, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100916', 'abnormal principal cavity', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(178400, 'HP:0030366', 'Delivery by Odon device', 'XPO:0101373', 'abnormal oxygen accumulating cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(178401, 'HP:0030366', 'Delivery by Odon device', 'XPO:0101472', 'abnormal zygote cortex', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(178402, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100643', 'abnormal thoracic region', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178403, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100372', 'abnormal hematological system', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(178404, 'HP:0030366', 'Delivery by Odon device', 'XPO:0101560', 'abnormal compound organ component', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178405, 'HP:0030366', 'Delivery by Odon device', 'XPO:0131667', 'abnormal actin cytoskeleton', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(178406, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100627', 'abnormal pharyngeal region', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(178407, 'HP:0030366', 'Delivery by Odon device', 'XPO:0101577', 'abnormal notochordal epithelium', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178408, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100551', 'abnormal oocyte cortex', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(178409, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100176', 'abnormal stage VI oocyte', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(178410, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100745', 'abnormal anterior lymph sac', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(178411, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100393', 'abnormal involuting marginal zone', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178412, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100444', 'abnormal cement gland', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178413, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100006', 'abnormal anatomical structure', 0.5294117647058824, 1.706362323152461, 0.9504568842024205, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178414, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100002', 'abnormal head', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(178415, 'HP:0030366', 'Delivery by Odon device', 'XPO:0101071', 'abnormal endoplasmic reticulum', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(178416, 'HP:0030366', 'Delivery by Odon device', 'XPO:0141777', 'abnormal catabolic process', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(178417, 'HP:0030366', 'Delivery by Odon device', 'XPO:0101535', 'abnormal absorptive cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(178418, 'HP:0030366', 'Delivery by Odon device', 'XPO:0107284', 'abnormal migrating myoblast', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(178419, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100727', 'abnormal odontogenic papilla', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(178420, 'HP:0030366', 'Delivery by Odon device', 'XPO:0107339', 'abnormal yolk platelet', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(178421, 'HP:0030366', 'Delivery by Odon device', 'XPO:0107270', 'abnormal proximal-distal axis', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178422, 'HP:0030366', 'Delivery by Odon device', 'XPO:0100309', 'abnormal vegetal hemisphere', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178423, 'HP:0005190', 'Proximal finger joint hyperextensibility', 'XPO:0102746', 'abnormal forelimb digit 2 morphology', 0.4791666666666667, 7.492661022682715, 1.8947911248214497, 'HP:0001167', 'Abnormal finger morphology'),
(178424, 'HP:0005190', 'Proximal finger joint hyperextensibility', 'XPO:0102529', 'abnormal forelimb digit 4 morphology', 0.4791666666666667, 7.492661022682715, 1.8947911248214497, 'HP:0001167', 'Abnormal finger morphology'),
(178425, 'HP:0005190', 'Proximal finger joint hyperextensibility', 'XPO:0103755', 'increased size of the forelimb digit', 0.4423076923076923, 7.492661022682715, 1.820456427983539, 'HP:0001167', 'Abnormal finger morphology'),
(178426, 'HP:0005190', 'Proximal finger joint hyperextensibility', 'XPO:0141208', 'abnormally necrotic digit-joint region', 0.40476190476190477, 6.466375519622663, 1.617820284280124, 'UPHENO:0086700', 'abnormal digit morphology'),
(178427, 'HP:0005190', 'Proximal finger joint hyperextensibility', 'XPO:0129652', 'increased size of the forelimb digit 3', 0.42990654205607476, 7.492661022682715, 1.7947545768321247, 'HP:0001167', 'Abnormal finger morphology'),
(178428, 'HP:0005190', 'Proximal finger joint hyperextensibility', 'XPO:0103465', 'bifurcated forelimb digit 2', 0.40707964601769914, 7.492661022682715, 1.7464563541194758, 'HP:0001167', 'Abnormal finger morphology'),
(178429, 'HP:0005190', 'Proximal finger joint hyperextensibility', 'XPO:0102214', 'abnormal forelimb digit morphology', 0.48936170212765956, 7.492661022682715, 1.914842382945809, 'HP:0001167', 'Abnormal finger morphology'),
(178430, 'HP:0005190', 'Proximal finger joint hyperextensibility', 'XPO:0140898', 'abnormally necrotic forelimb digit 5', 0.4380952380952381, 7.492661022682715, 1.8117668488795942, 'HP:0001167', 'Abnormal finger morphology'),
(178431, 'HP:0005190', 'Proximal finger joint hyperextensibility', 'XPO:0141556', 'abnormal forelimb digit morphology in the regenerating forelimb', 0.46, 7.492661022682715, 1.8565085699866966, 'HP:0001167', 'Abnormal finger morphology'),
(178432, 'HP:0005190', 'Proximal finger joint hyperextensibility', 'XPO:0140219', 'abnormally necrotic forelimb digit', 0.45098039215686275, 7.492661022682715, 1.8382173990874668, 'HP:0001167', 'Abnormal finger morphology'),
(178433, 'HP:0005190', 'Proximal finger joint hyperextensibility', 'XPO:0133378', 'fused forelimb digits part of regenerating forelimb', 0.41818181818181815, 7.492661022682715, 1.7701114680961476, 'HP:0001167', 'Abnormal finger morphology'),
(178434, 'HP:0005190', 'Proximal finger joint hyperextensibility', 'XPO:0130664', 'increased size of the forelimb digit 2', 0.42990654205607476, 7.492661022682715, 1.7947545768321247, 'HP:0001167', 'Abnormal finger morphology'),
(178435, 'HP:0005190', 'Proximal finger joint hyperextensibility', 'XPO:0103432', 'decreased size of the forelimb digit', 0.4380952380952381, 7.492661022682715, 1.8117668488795942, 'HP:0001167', 'Abnormal finger morphology'),
(178436, 'HP:0005190', 'Proximal finger joint hyperextensibility', 'XPO:0128172', 'decreased size of the forelimb digit 3', 0.42592592592592593, 7.492661022682715, 1.7864262043911108, 'HP:0001167', 'Abnormal finger morphology'),
(178437, 'HP:0005190', 'Proximal finger joint hyperextensibility', 'XPO:0130637', 'increased size of the forelimb digit 5', 0.42990654205607476, 7.492661022682715, 1.7947545768321247, 'HP:0001167', 'Abnormal finger morphology'),
(178438, 'HP:0005190', 'Proximal finger joint hyperextensibility', 'XPO:0103467', 'bifurcated forelimb digit 4', 0.40707964601769914, 7.492661022682715, 1.7464563541194758, 'HP:0001167', 'Abnormal finger morphology'),
(178439, 'HP:0005190', 'Proximal finger joint hyperextensibility', 'XPO:0140716', 'abnormally necrotic forelimb digit 4', 0.4380952380952381, 7.492661022682715, 1.8117668488795942, 'HP:0001167', 'Abnormal finger morphology'),
(178440, 'HP:0005190', 'Proximal finger joint hyperextensibility', 'XPO:0129161', 'decreased size of the forelimb digit 5', 0.42592592592592593, 7.492661022682715, 1.7864262043911108, 'HP:0001167', 'Abnormal finger morphology'),
(178441, 'HP:0005190', 'Proximal finger joint hyperextensibility', 'XPO:0101810', 'abnormal digit morphology', 0.425, 6.466375519622663, 1.657772480118919, 'UPHENO:0086700', 'abnormal digit morphology'),
(178442, 'HP:0005190', 'Proximal finger joint hyperextensibility', 'XPO:0141108', 'abnormally necrotic forelimb digit 2', 0.4380952380952381, 7.492661022682715, 1.8117668488795942, 'HP:0001167', 'Abnormal finger morphology'),
(178443, 'HP:0005190', 'Proximal finger joint hyperextensibility', 'XPO:0103468', 'bifurcated forelimb digit 5', 0.40707964601769914, 7.492661022682715, 1.7464563541194758, 'HP:0001167', 'Abnormal finger morphology'),
(178444, 'HP:0005190', 'Proximal finger joint hyperextensibility', 'XPO:0130624', 'increased size of the forelimb digit 4', 0.42990654205607476, 7.492661022682715, 1.7947545768321247, 'HP:0001167', 'Abnormal finger morphology'),
(178445, 'HP:0005190', 'Proximal finger joint hyperextensibility', 'XPO:0129148', 'decreased size of the forelimb digit 4', 0.42592592592592593, 7.492661022682715, 1.7864262043911108, 'HP:0001167', 'Abnormal finger morphology'),
(178446, 'HP:0005190', 'Proximal finger joint hyperextensibility', 'XPO:0103466', 'bifurcated forelimb digit 3', 0.40707964601769914, 7.492661022682715, 1.7464563541194758, 'HP:0001167', 'Abnormal finger morphology'),
(178447, 'HP:0005190', 'Proximal finger joint hyperextensibility', 'XPO:0102787', 'abnormal forelimb digit 5 morphology', 0.4791666666666667, 7.492661022682715, 1.8947911248214497, 'HP:0001167', 'Abnormal finger morphology'),
(178448, 'HP:0005190', 'Proximal finger joint hyperextensibility', 'XPO:0133358', 'fused forelimb digits', 0.44660194174757284, 7.492661022682715, 1.829272249170816, 'HP:0001167', 'Abnormal finger morphology'),
(178449, 'HP:0005190', 'Proximal finger joint hyperextensibility', 'XPO:0125257', 'absent forelimb digit', 0.40350877192982454, 7.492661022682715, 1.7387795857293602, 'HP:0001167', 'Abnormal finger morphology'),
(178450, 'HP:0005190', 'Proximal finger joint hyperextensibility', 'XPO:0103779', 'decreased size of the forelimb digit in the regenerating forelimb', 0.4107142857142857, 7.492661022682715, 1.7542357082303395, 'HP:0001167', 'Abnormal finger morphology'),
(178451, 'HP:0005190', 'Proximal finger joint hyperextensibility', 'XPO:0129188', 'decreased size of the forelimb digit 2', 0.42592592592592593, 7.492661022682715, 1.7864262043911108, 'HP:0001167', 'Abnormal finger morphology'),
(178452, 'HP:0005190', 'Proximal finger joint hyperextensibility', 'XPO:0102880', 'abnormal digit-joint region morphology', 0.425, 6.466375519622663, 1.657772480118919, 'UPHENO:0086700', 'abnormal digit morphology'),
(178453, 'HP:0005190', 'Proximal finger joint hyperextensibility', 'XPO:0141143', 'abnormally necrotic forelimb digit 3', 0.4380952380952381, 7.492661022682715, 1.8117668488795942, 'HP:0001167', 'Abnormal finger morphology'),
(178454, 'HP:0005190', 'Proximal finger joint hyperextensibility', 'XPO:0102598', 'abnormal forelimb digit 3 morphology', 0.4791666666666667, 7.492661022682715, 1.8947911248214497, 'HP:0001167', 'Abnormal finger morphology'),
(178455, 'HP:0012199', 'Cluster headache', 'XPO:0100164', 'abnormal neural nucleus', 0.4482758620689655, 3.94131651835137, 1.3292091859262085, 'UPHENO:0004523', 'abnormal nervous system'),
(178456, 'HP:0012199', 'Cluster headache', 'XPO:0100691', 'abnormal keratin accumulating cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(178457, 'HP:0012199', 'Cluster headache', 'XPO:0100289', 'abnormal chondroblast', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(178458, 'HP:0012199', 'Cluster headache', 'XPO:0100653', 'abnormal myoblast', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(178459, 'HP:0012199', 'Cluster headache', 'XPO:0100285', 'abnormal progenitor cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(178460, 'HP:0012199', 'Cluster headache', 'XPO:0100344', 'abnormal portion of organism substance', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178461, 'HP:0012199', 'Cluster headache', 'XPO:0100274', 'abnormal sensory system', 0.48148148148148145, 3.94131651835137, 1.3775597686645948, 'UPHENO:0004523', 'abnormal nervous system'),
(178462, 'HP:0012199', 'Cluster headache', 'XPO:0101501', 'abnormal parabrachial area', 0.43333333333333335, 3.94131651835137, 1.3068679445984308, 'UPHENO:0004523', 'abnormal nervous system'),
(178463, 'HP:0012199', 'Cluster headache', 'XPO:0101435', 'abnormal paracrine cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(178464, 'HP:0012199', 'Cluster headache', 'XPO:0100715', 'abnormal ciliated cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(178465, 'HP:0012199', 'Cluster headache', 'XPO:0107253', 'abnormal enteric nervous system', 0.48148148148148145, 3.94131651835137, 1.3775597686645948, 'UPHENO:0004523', 'abnormal nervous system'),
(178466, 'HP:0012199', 'Cluster headache', 'XPO:0100158', 'abnormal neuromere', 0.43333333333333335, 3.94131651835137, 1.3068679445984308, 'UPHENO:0004523', 'abnormal nervous system'),
(178467, 'HP:0012199', 'Cluster headache', 'XPO:0100427', 'abnormal olfactory system', 0.4642857142857143, 3.94131651835137, 1.3527368387638634, 'UPHENO:0004523', 'abnormal nervous system'),
(178468, 'HP:0012199', 'Cluster headache', 'XPO:0100587', 'abnormal vestibuloauditory system', 0.4642857142857143, 3.94131651835137, 1.3527368387638634, 'UPHENO:0004523', 'abnormal nervous system'),
(178469, 'HP:0012199', 'Cluster headache', 'XPO:0100537', 'abnormal medium cavity', 0.43333333333333335, 3.94131651835137, 1.3068679445984308, 'UPHENO:0004523', 'abnormal nervous system'),
(178470, 'HP:0012199', 'Cluster headache', 'XPO:0100916', 'abnormal principal cavity', 0.43333333333333335, 3.94131651835137, 1.3068679445984308, 'UPHENO:0004523', 'abnormal nervous system'),
(178471, 'HP:0012199', 'Cluster headache', 'XPO:0101132', 'abnormal apoptotic cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(178472, 'HP:0012199', 'Cluster headache', 'XPO:0100026', 'abnormal germ cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(178473, 'HP:0012199', 'Cluster headache', 'XPO:0101297', 'abnormal barrier cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(178474, 'HP:0012199', 'Cluster headache', 'XPO:0101448', 'abnormal myelin accumulating cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(178475, 'HP:0012199', 'Cluster headache', 'XPO:0100056', 'abnormal olfactory epithelium', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(178476, 'HP:0012199', 'Cluster headache', 'XPO:0100642', 'abnormal gustatory system', 0.4642857142857143, 3.94131651835137, 1.3527368387638634, 'UPHENO:0004523', 'abnormal nervous system'),
(178477, 'HP:0012199', 'Cluster headache', 'XPO:0101239', 'abnormal olfactory epithelial support cell', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(178478, 'HP:0012199', 'Cluster headache', 'XPO:0100734', 'abnormal lateral line system', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(178479, 'HP:0012199', 'Cluster headache', 'XPO:0100858', 'abnormal presumptive midbrain-hindbrain boundary', 0.43333333333333335, 3.94131651835137, 1.3068679445984308, 'UPHENO:0004523', 'abnormal nervous system'),
(178480, 'HP:0012199', 'Cluster headache', 'XPO:0100477', 'abnormal pericyte', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(178481, 'HP:0012199', 'Cluster headache', 'XPO:0100032', 'abnormal nervous system', 0.5, 3.94131651835137, 1.4038013602984167, 'UPHENO:0004523', 'abnormal nervous system'),
(178482, 'HP:0012199', 'Cluster headache', 'XPO:0100954', 'abnormal neural progenitor cell', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(178483, 'HP:0012199', 'Cluster headache', 'XPO:0100701', 'abnormal microglial cell', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(178484, 'HP:0012199', 'Cluster headache', 'XPO:0101467', 'abnormal alkali secreting cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(178485, 'HP:0012199', 'Cluster headache', 'XPO:0100704', 'abnormal Merkel cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(178486, 'HP:0012199', 'Cluster headache', 'XPO:0101373', 'abnormal oxygen accumulating cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(178487, 'HP:0012199', 'Cluster headache', 'XPO:0100638', 'abnormal polar body', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(178488, 'HP:0012199', 'Cluster headache', 'XPO:0100273', 'abnormal visual system', 0.4642857142857143, 3.94131651835137, 1.3527368387638634, 'UPHENO:0004523', 'abnormal nervous system'),
(178489, 'HP:0012199', 'Cluster headache', 'XPO:0100006', 'abnormal anatomical structure', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178490, 'HP:0012199', 'Cluster headache', 'XPO:0100175', 'abnormal migrating neuroblast', 0.43333333333333335, 3.94131651835137, 1.3068679445984308, 'UPHENO:0004523', 'abnormal nervous system'),
(178491, 'HP:0012199', 'Cluster headache', 'XPO:0100533', 'abnormal melanoblast', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(178492, 'HP:0012199', 'Cluster headache', 'XPO:0131654', 'abnormal neuron projection', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(178493, 'HP:0012199', 'Cluster headache', 'XPO:0100081', 'abnormal anatomical entity in vitro', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178494, 'HP:0012199', 'Cluster headache', 'XPO:0100114', 'abnormal peripheral nervous system', 0.4482758620689655, 3.94131651835137, 1.3292091859262085, 'UPHENO:0004523', 'abnormal nervous system'),
(178495, 'HP:0012199', 'Cluster headache', 'XPO:0100358', 'abnormal ganglion', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(178496, 'HP:0012199', 'Cluster headache', 'XPO:0100438', 'abnormal spinal cord', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(178497, 'HP:0012199', 'Cluster headache', 'XPO:0100108', 'abnormal cell part', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(178498, 'HP:0012199', 'Cluster headache', 'XPO:0100864', 'abnormal dorsolateral ascending neuron', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(178499, 'HP:0012199', 'Cluster headache', 'XPO:0100337', 'abnormal zygote', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(178500, 'HP:0012199', 'Cluster headache', 'XPO:0100760', 'abnormal Stirnorgan', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(178501, 'HP:0012199', 'Cluster headache', 'XPO:0100336', 'abnormal interneuron', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(178502, 'HP:0012199', 'Cluster headache', 'XPO:0107287', 'abnormal afferent neuron', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(178503, 'HP:0012199', 'Cluster headache', 'XPO:0101133', 'abnormal motor neuron', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(178504, 'HP:0012199', 'Cluster headache', 'XPO:0126887', 'abnormally localised nervous system', 0.4117647058823529, 3.94131651835137, 1.2739289764222381, 'UPHENO:0004523', 'abnormal nervous system'),
(178505, 'HP:0012199', 'Cluster headache', 'XPO:0101241', 'abnormal nucleate erythrocyte', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(178506, 'HP:0012199', 'Cluster headache', 'XPO:0107286', 'abnormal efferent neuron', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(178507, 'HP:0012199', 'Cluster headache', 'XPO:0100004', 'abnormal cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(178508, 'HP:0012199', 'Cluster headache', 'XPO:0101326', 'abnormal cementoblast', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(178509, 'HP:0012199', 'Cluster headache', 'XPO:0101535', 'abnormal absorptive cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(178510, 'HP:0012199', 'Cluster headache', 'XPO:0100852', 'abnormal interdigital region', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(178511, 'HP:0012199', 'Cluster headache', 'XPO:0100754', 'abnormal electrically active cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(178512, 'HP:0012199', 'Cluster headache', 'XPO:0100481', 'abnormal anatomical line', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178513, 'HP:0012199', 'Cluster headache', 'XPO:0101187', 'abnormal dorsolateral commissural neuron', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(178514, 'HP:0012199', 'Cluster headache', 'XPO:0101237', 'abnormal mucus secreting cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(178515, 'HP:0012199', 'Cluster headache', 'XPO:0101333', 'abnormal barrier epithelial cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(178516, 'HP:0012199', 'Cluster headache', 'XPO:0100172', 'abnormal stem cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(178517, 'HP:0012199', 'Cluster headache', 'XPO:0142051', 'abnormal cerebrospinal fluid', 0.4482758620689655, 3.94131651835137, 1.3292091859262085, 'UPHENO:0004523', 'abnormal nervous system'),
(178518, 'HP:0012199', 'Cluster headache', 'XPO:0100031', 'abnormal central nervous system', 0.48148148148148145, 3.94131651835137, 1.3775597686645948, 'UPHENO:0004523', 'abnormal nervous system'),
(178519, 'HP:0012199', 'Cluster headache', 'XPO:0100549', 'abnormal mitotic cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(178520, 'HP:0012199', 'Cluster headache', 'XPO:0100196', 'abnormal neuron', 0.43333333333333335, 3.94131651835137, 1.3068679445984308, 'UPHENO:0004523', 'abnormal nervous system'),
(178521, 'HP:0012199', 'Cluster headache', 'XPO:0100702', 'abnormal glial cell', 0.43333333333333335, 3.94131651835137, 1.3068679445984308, 'UPHENO:0004523', 'abnormal nervous system'),
(178522, 'HP:0012199', 'Cluster headache', 'XPO:0100802', 'abnormal exocrine cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(178523, 'HP:0012199', 'Cluster headache', 'XPO:0100791', 'abnormal multiciliated cell precursor', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(178524, 'HP:0012199', 'Cluster headache', 'XPO:0101004', 'abnormal acid secreting cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(178525, 'HP:0006694', 'Early progressive calcific cardiac valvular disease', 'XPO:0101995', 'abnormal cardiovascular system morphology', 0.40425531914893614, 5.9590888072311134, 1.552093214856655, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(178526, 'HP:0006694', 'Early progressive calcific cardiac valvular disease', 'XPO:0102769', 'abnormal cardiac valve morphology', 0.43333333333333335, 10.21769640676594, 2.1042025669910935, 'UPHENO:0015319', 'abnormal cardiac valve morphology in the heart'),
(178527, 'HP:0006694', 'Early progressive calcific cardiac valvular disease', 'XPO:0101900', 'abnormal circulatory system morphology', 0.40425531914893614, 5.9590888072311134, 1.552093214856655, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(178528, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0101349', 'abnormal trunk region', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178529, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100458', 'abnormal autopod', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(178530, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0107288', 'abnormal larval alimentary system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(178531, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0142057', 'abnormal desmosome', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(178532, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100282', 'abnormal pelvic girdle primordium', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178533, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0101587', 'abnormal hemangioblast', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(178534, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0101322', 'abnormal iridophore', 0.40625, 6.4952303822948485, 1.624403688375301, 'UPHENO:0002635', 'abnormal integument'),
(178535, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100691', 'abnormal keratin accumulating cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(178536, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0141770', 'abnormal urate homeostasis', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(178537, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0116434', 'abnormal biological process', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(178538, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100225', 'abnormal endocrine system', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(178539, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100014', 'abnormal tissue', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178540, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100827', 'abnormal atypical epithelium', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178541, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100239', 'abnormal acellular anatomical structure', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178542, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100843', 'abnormal fasciculated network of fibrils', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(178543, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100114', 'abnormal peripheral nervous system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(178544, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100626', 'abnormal primordial germ cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(178545, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0141271', 'increased surface breathing', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(178546, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0101387', 'abnormal melanophore', 0.40625, 6.4952303822948485, 1.624403688375301, 'UPHENO:0002635', 'abnormal integument'),
(178547, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100667', 'abnormal vegetal yolk mass', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178548, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0115391', 'abnormally undifferentiated alimentary system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(178549, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0131691', 'abnormal molecular function', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(178550, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0142054', 'abnormal digestive tract', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(178551, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0101480', 'abnormal stage V oocyte', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(178552, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100384', 'abnormal amputated tissue', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178553, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100277', 'abnormal blastocoel', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178554, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0101450', 'abnormal myeloid cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(178555, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100585', 'abnormal elastica externa', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(178556, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0107285', 'abnormal flexural organ', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(178557, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100028', 'abnormal anatomical cluster', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178558, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100890', 'abnormal pharyngeal cavity', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(178559, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100549', 'abnormal mitotic cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(178560, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100983', 'abnormal skin gland', 0.4642857142857143, 6.4952303822948485, 1.7365605884892232, 'HP:0001574', 'Abnormality of the integument'),
(178561, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0107265', 'abnormal posterior side', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178562, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100704', 'abnormal Merkel cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(178563, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100067', 'abnormal animal hemisphere', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178564, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100427', 'abnormal olfactory system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(178565, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100557', 'abnormal prime meridian', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178566, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0141499', 'abnormal tadpole', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178567, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100337', 'abnormal zygote', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(178568, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0141715', 'abnormal septum', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178569, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0101098', 'abnormal mineralized extracellular matrix', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178570, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0101240', 'abnormal ciliated non-epidermal cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(178571, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0131669', 'abnormal Roux spot', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(178572, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100394', 'abnormal marginal zone', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178573, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0101224', 'abnormal dorsal involuting marginal zone', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178574, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0141778', 'abnormal biosynthetic process', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(178575, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0101543', 'abnormal external gill', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(178576, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100674', 'abnormal secondary oogonium', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(178577, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0101141', 'abnormal Keller explant', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178578, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100573', 'abnormal extraembryonic structure', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178579, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100162', 'abnormal presumptive rhombomere', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178580, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0141497', 'abnormal lymphoblast', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(178581, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100856', 'abnormal simple organ', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178582, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100588', 'abnormal unicellular gland', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178583, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0107284', 'abnormal migrating myoblast', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(178584, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0101071', 'abnormal endoplasmic reticulum', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(178585, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100372', 'abnormal hematological system', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(178586, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0101297', 'abnormal barrier cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(178587, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0101278', 'abnormal pigment cell', 0.41935483870967744, 6.4952303822948485, 1.650395797785929, 'UPHENO:0002635', 'abnormal integument'),
(178588, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0101389', 'abnormal wedge region', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(178589, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100196', 'abnormal neuron', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(178590, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100754', 'abnormal electrically active cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(178591, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0116494', 'absent biological process', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(178592, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0101503', 'abnormal organ cortex', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178593, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100612', 'abnormal unilaminar epithelium', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178594, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100108', 'abnormal cell part', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(178595, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100553', 'abnormal laryngeal muscle primordium', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178596, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100642', 'abnormal gustatory system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(178597, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100574', 'abnormal gastrula cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(178598, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0101366', 'abnormal morula cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(178599, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0107311', 'abnormal apical junction complex', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(178600, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100249', 'abnormal avascular GAG-rich matrix', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178601, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100296', 'abnormal tail region', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178602, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0101010', 'abnormal dorsal marginal zone', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178603, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100888', 'abnormal microtubule', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(178604, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100135', 'abnormal surface structure', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178605, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100192', 'abnormal epithelium', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178606, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100816', 'abnormal blastocoel anlage', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178607, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100640', 'abnormal notochordal sheath', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(178608, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100581', 'abnormal immune system', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(178609, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0101099', 'abnormal ventro-lateral marginal zone', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178610, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100511', 'abnormal stylopod', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(178611, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0101497', 'abnormal ciliary axoneme', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(178612, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100999', 'abnormal serous membrane', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178613, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100605', 'abnormal prechordal plate', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178614, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0107259', 'abnormal animal-vegetal axis', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178615, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0101254', 'abnormal stratum compactum', 0.41935483870967744, 6.4952303822948485, 1.650395797785929, 'HP:0001574', 'Abnormality of the integument'),
(178616, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0101241', 'abnormal nucleate erythrocyte', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(178617, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100994', 'abnormal granular gland', 0.4482758620689655, 6.4952303822948485, 1.7063572307578971, 'HP:0001574', 'Abnormality of the integument'),
(178618, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100468', 'abnormal muscular system', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178619, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0107253', 'abnormal enteric nervous system', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(178620, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0101467', 'abnormal alkali secreting cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(178621, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0141796', 'abnormal demethylation', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(178622, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0141792', 'abnormal small molecule metabolic process', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(178623, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100665', 'abnormal egg jelly', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178624, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100339', 'abnormal circumblastoporal collar', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178625, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0101448', 'abnormal myelin accumulating cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(178626, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100907', 'abnormal cytoplasm', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(178627, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100728', 'abnormal cell condensation', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178628, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0141264', 'abnormal schooling behavior', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(178629, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100393', 'abnormal involuting marginal zone', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178630, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100887', 'abnormal right-dorsal blastomere', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(178631, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:00000000', 'Xenopus phenotype', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(178632, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100308', 'abnormal early embryonic cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(178633, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100900', 'abnormal angioblast', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(178634, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100151', 'abnormal primordium', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178635, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100868', 'abnormal transporting epithelium', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178636, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100807', 'abnormal matrix-based tissue', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178637, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100916', 'abnormal principal cavity', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(178638, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0101029', 'abnormal right spleen primordium', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(178639, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0141904', 'abnormal glucosamine metabolic process', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(178640, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100800', 'abnormal ventral marginal zone', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178641, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100515', 'abnormal somatic stem cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(178642, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0107339', 'abnormal yolk platelet', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(178643, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100031', 'abnormal central nervous system', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(178644, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100084', 'abnormal anatomical group', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178645, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100643', 'abnormal thoracic region', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178646, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100317', 'abnormal respiratory system', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(178647, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100437', 'abnormal proepicardium', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(178648, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100842', 'abnormal left-dorsal blastomere', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(178649, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100203', 'abnormal endocrine cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(178650, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0101405', 'abnormal ring structure', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(178651, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0141276', 'decreased surface breathing', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(178652, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100449', 'abnormal lymphocyte', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(178653, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0101157', 'abnormal female organism', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178654, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0107272', 'abnormal axial region', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178655, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0141266', 'abnormal surface breathing', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(178656, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0101570', 'abnormal forelimb region', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178657, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100002', 'abnormal head', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(178658, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100205', 'abnormal limb segment', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(178659, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100902', 'abnormal spermatocyte', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(178660, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0101424', 'abnormal coelomic epithelium', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178661, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100164', 'abnormal neural nucleus', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(178662, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0101326', 'abnormal cementoblast', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(178663, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0141745', 'abnormal creatinine homeostasis', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(178664, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100786', 'abnormal presumptive axial mesoderm', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178665, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100482', 'abnormal Mullerian duct', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(178666, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0101976', 'abnormal portion of organism substance morphology', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178667, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0141772', 'abnormal water homeostasis', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(178668, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100307', 'abnormal blastomere', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(178669, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100913', 'abnormal Brachets cleft', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178670, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0101547', 'abnormal lampbrush chromosome', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(178671, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0107273', 'abnormal basal region', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178672, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100231', 'abnormal compound organ', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178673, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0101095', 'abnormal skin seromucous gland', 0.4482758620689655, 6.4952303822948485, 1.7063572307578971, 'UPHENO:0002635', 'abnormal integument'),
(178674, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0101109', 'abnormal egg cell-free extract', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178675, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100802', 'abnormal exocrine cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(178676, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0101713', 'abnormal anatomical entity in vitro morphology', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178677, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0107267', 'abnormal ventral side', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178678, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0142056', 'abnormal main body axis', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178679, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100202', 'abnormal embryo', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178680, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0101174', 'abnormal articular system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(178681, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0101409', 'abnormal perivitelline space', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(178682, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100060', 'abnormal regenerating tissue', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178683, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100599', 'abnormal adult immune system', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(178684, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100444', 'abnormal cement gland', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178685, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100533', 'abnormal melanoblast', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(178686, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0101406', 'abnormal cleavage furrow', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178687, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100010', 'abnormal multicellular anatomical structure', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178688, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100493', 'abnormal liver and biliary system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(178689, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0101004', 'abnormal acid secreting cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(178690, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0141714', 'abnormal anterior notochord', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(178691, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100638', 'abnormal polar body', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(178692, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0131723', 'abnormal pathway-restricted SMAD protein phosphorylation', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(178693, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100378', 'abnormal perichondrium', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(178694, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0101591', 'abnormal xanthophore', 0.40625, 6.4952303822948485, 1.624403688375301, 'HP:0001574', 'Abnormality of the integument'),
(178695, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100915', 'abnormal dermal system', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178696, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0141748', 'abnormal gas homeostasis', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(178697, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0131687', 'abnormal astral microtubule', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(178698, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0101132', 'abnormal apoptotic cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(178699, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100273', 'abnormal visual system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(178700, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100796', 'abnormal pseudoblastema', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178701, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0115512', 'abnormally semi-erect whole organism', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178702, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0101221', 'abnormal larval immune system', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(178703, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100232', 'abnormal lymphatic system', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(178704, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100862', 'abnormal blastomere V1', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(178705, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100894', 'abnormal nucleus', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(178706, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100509', 'abnormal germ plasm', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(178707, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0107312', 'abnormal filopodium', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(178708, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100261', 'abnormal multilaminar epithelium', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178709, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0107278', 'abnormal medial region', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178710, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100386', 'abnormal limb', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(178711, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100899', 'abnormal secondary spermatogonium', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(178712, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100976', 'abnormal multiciliated cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(178713, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0141797', 'abnormal hydrogen metabolic process', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(178714, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100707', 'abnormal central vegetal yolk mass', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178715, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100081', 'abnormal anatomical entity in vitro', 0.5294117647058824, 1.706362323152461, 0.9504568842024205, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178716, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0101529', 'abnormal skin mucous gland', 0.41935483870967744, 6.4952303822948485, 1.650395797785929, 'UPHENO:0002635', 'abnormal integument'),
(178717, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100991', 'abnormal iliac process primordium', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178718, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0141790', 'abnormal cellular metabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(178719, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100003', 'abnormal organism subdivision', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178720, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100465', 'abnormal skeletal system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(178721, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100201', 'abnormal cavitated compound organ', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178722, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0101461', 'abnormal sperm entry point', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(178723, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100653', 'abnormal myoblast', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(178724, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0107268', 'abnormal left side', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178725, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0141783', 'abnormal collagen metabolic process', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(178726, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0101228', 'abnormal mesenchymal stem cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(178727, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100791', 'abnormal multiciliated cell precursor', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(178728, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0101535', 'abnormal absorptive cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(178729, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0101362', 'abnormal vegetal cortex', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(178730, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100484', 'abnormal cement gland primordium', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178731, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100285', 'abnormal progenitor cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(178732, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0141776', 'abnormal metabolic process', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(178733, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100009', 'abnormal multi-tissue structure', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178734, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100956', 'abnormal centrosome', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(178735, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0101472', 'abnormal zygote cortex', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(178736, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100207', 'abnormal blastema', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178737, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0141860', 'abnormal malate-aspartate shuttle', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(178738, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0101560', 'abnormal compound organ component', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178739, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0101463', 'abnormal right-ventral blastomere', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(178740, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0141738', 'abnormal carbon dioxide homeostasis', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(178741, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0101136', 'abnormal ooplasm', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(178742, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100477', 'abnormal pericyte', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(178743, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100026', 'abnormal germ cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(178744, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0101577', 'abnormal notochordal epithelium', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178745, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100120', 'abnormal genital system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(178746, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100547', 'abnormal blastomere V2', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(178747, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0141786', 'abnormal pigment metabolic process', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(178748, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100846', 'abnormal hindlimb', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(178749, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0101573', 'abnormal peripheral vegetal yolk mass', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178750, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100415', 'abnormal secretory epithelial cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(178751, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0141782', 'abnormal methylation', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(178752, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100006', 'abnormal anatomical structure', 0.5294117647058824, 1.706362323152461, 0.9504568842024205, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178753, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100258', 'abnormal organ part', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178754, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0101200', 'abnormal joint region', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178755, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100422', 'abnormal notochord', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(178756, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0101113', 'abnormal stage IV oocyte', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(178757, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100781', 'abnormal presumptive ectoderm', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178758, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0107258', 'abnormal anatomical axis', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178759, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100715', 'abnormal ciliated cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(178760, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100784', 'abnormal left blastomere', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(178761, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0101176', 'abnormal non-ciliated epithelial cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(178762, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100503', 'abnormal blastomere D2', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(178763, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0141771', 'abnormal urea homeostasis', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(178764, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0141265', 'abnormal escape behavior', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(178765, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0107264', 'abnormal anterior side', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178766, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100363', 'abnormal cardiovascular system', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178767, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0141743', 'abnormal chemical homeostasis within a tissue', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(178768, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100251', 'abnormal proteinaceous extracellular matrix', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178769, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100062', 'abnormal anatomical space', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178770, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100688', 'abnormal adipose tissue', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(178771, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100551', 'abnormal oocyte cortex', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(178772, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100501', 'abnormal urogenital system', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(178773, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100295', 'abnormal extracellular matrix', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178774, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0131685', 'abnormal cortical actin cytoskeleton', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(178775, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100423', 'abnormal process', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178776, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100969', 'abnormal disaggregated/reaggregated ectoderm treated with activin', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178777, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100627', 'abnormal pharyngeal region', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(178778, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0141794', 'abnormal prosthetic group metabolic process', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(178779, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100858', 'abnormal presumptive midbrain-hindbrain boundary', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(178780, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100416', 'abnormal ligament', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(178781, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0101638', 'abnormal anatomical structure morphology', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178782, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0101575', 'abnormal vitelline membrane', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(178783, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100289', 'abnormal chondroblast', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(178784, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100104', 'abnormal embryonic structure', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178785, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100481', 'abnormal anatomical line', 0.5294117647058824, 1.706362323152461, 0.9504568842024205, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178786, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0107271', 'abnormal apical region', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178787, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100587', 'abnormal vestibuloauditory system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(178788, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0101569', 'abnormal activin-induced ectoderm', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178789, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0101078', 'abnormal mucous gland', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178790, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0131666', 'abnormal adherens junction', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(178791, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0101519', 'abnormal hypobranchial placode', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178792, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0102113', 'abnormal anatomical line morphology', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178793, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0101220', 'abnormal centriole', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(178794, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100852', 'abnormal interdigital region', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(178795, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100218', 'abnormal epithelial cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(178796, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100293', 'abnormal duct', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178797, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0141263', 'abnormal visually guided collision avoidance behavior', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(178798, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0101313', 'abnormal Eberth-Kastschenko layer', 0.41935483870967744, 6.4952303822948485, 1.650395797785929, 'UPHENO:0002635', 'abnormal integument'),
(178799, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100610', 'abnormal appendage', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178800, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100917', 'abnormal stage III oocyte', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(178801, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100417', 'abnormal dense regular connective tissue', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(178802, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0131677', 'abnormal actin filament', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(178803, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100032', 'abnormal nervous system', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(178804, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100823', 'abnormal blood', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(178805, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100268', 'abnormal circulatory system', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178806, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0101074', 'abnormal germinal vesicle', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(178807, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100023', 'abnormal mesenchyme', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178808, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100152', 'abnormal alimentary system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(178809, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0107270', 'abnormal proximal-distal axis', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178810, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0107262', 'abnormal left-right axis', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178811, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100507', 'abnormal skin', 0.48148148148148145, 6.4952303822948485, 1.7684267434730943, 'HP:0001574', 'Abnormality of the integument'),
(178812, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0101264', 'abnormal mitotic spindle', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(178813, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100545', 'abnormal male organism', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178814, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0141777', 'abnormal catabolic process', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(178815, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100392', 'abnormal cilium', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(178816, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0107261', 'abnormal dorsal-ventral axis', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178817, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100004', 'abnormal cell', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(178818, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0101451', 'abnormal dorsal lymph space', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(178819, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0107263', 'abnormal anatomical side', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178820, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0142051', 'abnormal cerebrospinal fluid', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(178821, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100544', 'abnormal neuromast support cell', 0.41935483870967744, 6.4952303822948485, 1.650395797785929, 'UPHENO:0002635', 'abnormal integument'),
(178822, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100133', 'abnormal solid compound organ', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178823, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0101040', 'abnormal axial mesoderm', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178824, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0101333', 'abnormal barrier epithelial cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(178825, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100274', 'abnormal sensory system', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(178826, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0115758', 'abnormally decreased mobility of melanoblast', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(178827, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0101061', 'abnormal plasma membrane', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(178828, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100854', 'abnormal spiracle', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178829, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100722', 'abnormal barbel', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178830, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0141718', 'abnormal posterior notochord', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(178831, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0101373', 'abnormal oxygen accumulating cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(178832, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0141841', 'abnormality of whole organism mass', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(178833, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0107266', 'abnormal dorsal side', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178834, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0101110', 'abnormal cell-free extract', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178835, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100402', 'abnormal zeugopod', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(178836, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0141267', 'abnormal resting posture', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(178837, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100265', 'abnormal sensory epithelial cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(178838, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100025', 'abnormal oocyte', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(178839, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0101311', 'abnormal bottle cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(178840, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0101107', 'abnormal erythroid cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(178841, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0101513', 'abnormal basal body', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(178842, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0141787', 'abnormal hormone metabolic process', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(178843, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0115505', 'dead whole organism', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178844, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0101411', 'abnormal marginal zone (sensu neural)', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178845, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100309', 'abnormal vegetal hemisphere', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178846, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100158', 'abnormal neuromere', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(178847, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100742', 'abnormal musculoskeletal system', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178848, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100103', 'abnormal trunk', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178849, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0101168', 'abnormal circulating cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(178850, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0101212', 'abnormal glomeral mesenchyme', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(178851, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0115508', 'abnormally peramorphic growth of whole organism', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178852, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0101237', 'abnormal mucus secreting cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(178853, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100745', 'abnormal anterior lymph sac', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(178854, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100070', 'abnormal anatomical system', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178855, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100935', 'abnormal skeleton', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(178856, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0115509', 'abnormally semi-viable whole organism', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178857, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0101208', 'abnormal stratum spongiosum', 0.41935483870967744, 6.4952303822948485, 1.650395797785929, 'UPHENO:0002635', 'abnormal integument'),
(178858, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0101378', 'abnormal blastomere D1', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(178859, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0142052', 'abnormal nasal region', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(178860, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0101283', 'abnormal left-ventral blastomere', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(178861, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0101023', 'abnormal ultimobranchial body', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(178862, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0101092', 'abnormal dorso-lateral marginal zone', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178863, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100762', 'abnormal intersomitic region', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178864, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0131725', 'abnormal phosphorylation of RNA polymerase II C-terminal domain', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(178865, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0101468', 'abnormal stage I oocyte', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(178866, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100989', 'abnormal right blastomere', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(178867, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0107260', 'abnormal anterior-posterior axis', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178868, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0141775', 'abnormal nitrogen compound metabolic process', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(178869, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0101515', 'abnormal neuromast mantle cell', 0.41935483870967744, 6.4952303822948485, 1.650395797785929, 'HP:0001574', 'Abnormality of the integument'),
(178870, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0101498', 'abnormal stage II oocyte', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(178871, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100929', 'abnormal dermis', 0.4482758620689655, 6.4952303822948485, 1.7063572307578971, 'UPHENO:0002635', 'abnormal integument'),
(178872, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0131675', 'abnormal spindle microtubule', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(178873, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0101149', 'abnormal amputated limb', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178874, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0141272', 'absent surface breathing', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(178875, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0101347', 'abnormal hindlimb region', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178876, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100256', 'abnormal paired appendage', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178877, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0101435', 'abnormal paracrine cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(178878, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100721', 'abnormal centromere', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(178879, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100176', 'abnormal stage VI oocyte', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(178880, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100531', 'abnormal proliferative region', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178881, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0141784', 'abnormal cellular hormone metabolic process', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(178882, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0101096', 'abnormal tendon', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(178883, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100546', 'abnormal whole organism', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178884, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0101501', 'abnormal parabrachial area', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(178885, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0101553', 'abnormal dental epithelium', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178886, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0141781', 'abnormal secondary metabolic process', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(178887, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0107269', 'abnormal right side', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178888, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100377', 'abnormal connective tissue', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(178889, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100186', 'abnormal uveal tract', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178890, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100403', 'abnormal forelimb', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(178891, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100727', 'abnormal odontogenic papilla', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(178892, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100175', 'abnormal migrating neuroblast', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(178893, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100724', 'abnormal kinetochore', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(178894, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0107276', 'abnormal dorsal region', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178895, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100383', 'abnormal amputated fin', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178896, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100429', 'abnormal spermatid', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(178897, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0141315', 'abnormal anatomical region', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178898, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100912', 'abnormal trabecula', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178899, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100344', 'abnormal portion of organism substance', 0.5294117647058824, 1.706362323152461, 0.9504568842024205, 'UPHENO:0002536', 'abnormal anatomical entity'),
(178900, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0101072', 'abnormal mitochondrial cloud', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(178901, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0101302', 'abnormal subcortical cytoplasm', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(178902, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100702', 'abnormal glial cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(178903, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100537', 'abnormal medium cavity', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(178904, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100069', 'abnormal urinary system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(178905, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0141791', 'abnormal primary metabolic process', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(178906, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0131667', 'abnormal actin cytoskeleton', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(178907, 'HP:0007550', 'Hypohidrosis or hyperhidrosis', 'XPO:0100172', 'abnormal stem cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(178908, 'HP:0011218', 'Abnormal shape of the frontal region', 'XPO:0101986', 'abnormal amygdala morphology', 0.4117647058823529, 8.02346099791745, 1.8176297912297787, 'HP:0002060', 'Abnormal cerebral morphology'),
(178909, 'HP:0011218', 'Abnormal shape of the frontal region', 'XPO:0140421', 'abnormally necrotic anterior entopeduncular region', 0.4166666666666667, 8.02346099791745, 1.8284170063561187, 'HP:0002060', 'Abnormal cerebral morphology'),
(178910, 'HP:0011218', 'Abnormal shape of the frontal region', 'XPO:0101805', 'abnormal pallidum morphology', 0.4069767441860465, 8.02346099791745, 1.8070312764410503, 'HP:0002060', 'Abnormal cerebral morphology'),
(178911, 'HP:0011218', 'Abnormal shape of the frontal region', 'XPO:0129372', 'decreased size of the anterior entopeduncular region', 0.4069767441860465, 8.02346099791745, 1.8070312764410503, 'HP:0002060', 'Abnormal cerebral morphology'),
(178912, 'HP:0011218', 'Abnormal shape of the frontal region', 'XPO:0102828', 'abnormal occipital region morphology', 0.4050632911392405, 7.717194259133599, 1.768036228408657, 'UPHENO:0087814', 'abnormal cranium morphology'),
(178913, 'HP:0011218', 'Abnormal shape of the frontal region', 'XPO:0102007', 'abnormal anterior entopeduncular region morphology', 0.43209876543209874, 8.02346099791745, 1.8619687407936594, 'HP:0002060', 'Abnormal cerebral morphology'),
(178914, 'HP:0011218', 'Abnormal shape of the frontal region', 'XPO:0102249', 'abnormal forebrain morphology', 0.4074074074074074, 6.667568321314008, 1.6481555519726587, 'HP:0100547', 'Abnormal forebrain morphology'),
(178915, 'HP:0011218', 'Abnormal shape of the frontal region', 'XPO:0102357', 'abnormal subpallium morphology', 0.42168674698795183, 8.02346099791745, 1.8393985886143642, 'HP:0002060', 'Abnormal cerebral morphology'),
(178916, 'HP:0011218', 'Abnormal shape of the frontal region', 'XPO:0102238', 'abnormal basal forebrain morphology', 0.42168674698795183, 8.02346099791745, 1.8393985886143642, 'HP:0002060', 'Abnormal cerebral morphology'),
(178917, 'HP:0011218', 'Abnormal shape of the frontal region', 'XPO:0102696', 'abnormal accessory olfactory bulb morphology', 0.4044943820224719, 8.651717009412357, 1.870714014796372, 'UPHENO:0087531', 'abnormal cerebral hemisphere morphology'),
(178918, 'HP:0011218', 'Abnormal shape of the frontal region', 'XPO:0130846', 'increased size of the anterior entopeduncular region', 0.4069767441860465, 8.02346099791745, 1.8070312764410503, 'HP:0002060', 'Abnormal cerebral morphology'),
(178919, 'HP:0011218', 'Abnormal shape of the frontal region', 'XPO:0102604', 'abnormal ventral pallidum morphology', 0.40229885057471265, 8.02346099791745, 1.7966160238329245, 'HP:0002060', 'Abnormal cerebral morphology'),
(178920, 'HP:0011218', 'Abnormal shape of the frontal region', 'XPO:0102564', 'abnormal olfactory region morphology', 0.4177215189873418, 8.21064164923199, 1.8519615821009678, 'UPHENO:0088115', 'abnormal neurocranium morphology'),
(178921, 'HP:0011218', 'Abnormal shape of the frontal region', 'XPO:0102401', 'abnormal neurocranium morphology', 0.4177215189873418, 8.21064164923199, 1.8519615821009678, 'UPHENO:0088115', 'abnormal neurocranium morphology'),
(178922, 'HP:0011218', 'Abnormal shape of the frontal region', 'XPO:0102174', 'abnormal pallium morphology', 0.42168674698795183, 8.02346099791745, 1.8393985886143642, 'HP:0002060', 'Abnormal cerebral morphology'),
(178923, 'HP:0011218', 'Abnormal shape of the frontal region', 'XPO:0107380', 'abnormal dorsal telencephalon morphology', 0.42168674698795183, 8.02346099791745, 1.8393985886143642, 'HP:0002060', 'Abnormal cerebral morphology'),
(178924, 'HP:0011218', 'Abnormal shape of the frontal region', 'XPO:0102968', 'abnormal medial ganglionic eminence morphology', 0.4117647058823529, 8.02346099791745, 1.8176297912297787, 'HP:0002060', 'Abnormal cerebral morphology'),
(178925, 'HP:0011218', 'Abnormal shape of the frontal region', 'XPO:0103200', 'abnormal prosomere 5 morphology', 0.40229885057471265, 8.02346099791745, 1.7966160238329245, 'HP:0002060', 'Abnormal cerebral morphology'),
(178926, 'HP:0011218', 'Abnormal shape of the frontal region', 'XPO:0103152', 'abnormal otic region morphology', 0.4177215189873418, 8.21064164923199, 1.8519615821009678, 'UPHENO:0088115', 'abnormal neurocranium morphology'),
(178927, 'HP:0011218', 'Abnormal shape of the frontal region', 'XPO:0102978', 'abnormal prosomere 6 morphology', 0.40229885057471265, 8.02346099791745, 1.7966160238329245, 'HP:0002060', 'Abnormal cerebral morphology'),
(178928, 'HP:0011218', 'Abnormal shape of the frontal region', 'XPO:0102066', 'abnormal ventral pallium morphology', 0.4166666666666667, 8.02346099791745, 1.8284170063561187, 'HP:0002060', 'Abnormal cerebral morphology'),
(178929, 'HP:0011218', 'Abnormal shape of the frontal region', 'XPO:0102351', 'abnormal sphenoid region morphology', 0.4177215189873418, 8.21064164923199, 1.8519615821009678, 'UPHENO:0088115', 'abnormal neurocranium morphology'),
(178930, 'HP:0011218', 'Abnormal shape of the frontal region', 'XPO:0115310', 'abnormally incomplete structure of forebrain', 0.4024390243902439, 6.667568321314008, 1.6380749953176459, 'HP:0100547', 'Abnormal forebrain morphology'),
(178931, 'HP:0011218', 'Abnormal shape of the frontal region', 'XPO:0102389', 'abnormal bed nucleus of the stria terminalis morphology', 0.4044943820224719, 8.651717009412357, 1.870714014796372, 'UPHENO:0087531', 'abnormal cerebral hemisphere morphology'),
(178932, 'HP:0011218', 'Abnormal shape of the frontal region', 'XPO:0102442', 'abnormal medial pallium morphology', 0.4166666666666667, 8.02346099791745, 1.8284170063561187, 'HP:0002060', 'Abnormal cerebral morphology'),
(178933, 'HP:0011218', 'Abnormal shape of the frontal region', 'XPO:0102200', 'abnormal telencephalon septum morphology', 0.40229885057471265, 8.02346099791745, 1.7966160238329245, 'HP:0002060', 'Abnormal cerebral morphology'),
(178934, 'HP:0011218', 'Abnormal shape of the frontal region', 'XPO:0103178', 'abnormal dorsal pallium morphology', 0.4166666666666667, 8.02346099791745, 1.8284170063561187, 'HP:0002060', 'Abnormal cerebral morphology'),
(178935, 'HP:0011218', 'Abnormal shape of the frontal region', 'XPO:0102826', 'abnormal anterior commissure morphology', 0.4166666666666667, 8.02346099791745, 1.8284170063561187, 'HP:0002060', 'Abnormal cerebral morphology'),
(178936, 'HP:0011218', 'Abnormal shape of the frontal region', 'XPO:0101851', 'abnormal basal ganglion morphology', 0.4117647058823529, 8.02346099791745, 1.8176297912297787, 'HP:0002060', 'Abnormal cerebral morphology'),
(178937, 'HP:0011218', 'Abnormal shape of the frontal region', 'XPO:0103040', 'abnormal nucleus of the diagonal band morphology', 0.40229885057471265, 8.02346099791745, 1.7966160238329245, 'HP:0002060', 'Abnormal cerebral morphology'),
(178938, 'HP:0011218', 'Abnormal shape of the frontal region', 'XPO:0101987', 'abnormal striatum morphology', 0.4069767441860465, 8.02346099791745, 1.8070312764410503, 'HP:0002060', 'Abnormal cerebral morphology'),
(178939, 'HP:0011218', 'Abnormal shape of the frontal region', 'XPO:0139879', 'abnormally necrotic telencephalon', 0.40229885057471265, 8.02346099791745, 1.7966160238329245, 'HP:0002060', 'Abnormal cerebral morphology'),
(178940, 'HP:0011218', 'Abnormal shape of the frontal region', 'XPO:0101970', 'abnormal lateral ganglionic eminence morphology', 0.4117647058823529, 8.02346099791745, 1.8176297912297787, 'HP:0002060', 'Abnormal cerebral morphology'),
(178941, 'HP:0011218', 'Abnormal shape of the frontal region', 'XPO:0102760', 'abnormal dorsal pallidum morphology', 0.40229885057471265, 8.02346099791745, 1.7966160238329245, 'HP:0002060', 'Abnormal cerebral morphology'),
(178942, 'HP:0011218', 'Abnormal shape of the frontal region', 'XPO:0102191', 'abnormal telencephalon morphology', 0.4268292682926829, 8.02346099791745, 1.8505804459455375, 'HP:0002060', 'Abnormal cerebral morphology'),
(178943, 'HP:0011218', 'Abnormal shape of the frontal region', 'XPO:0101797', 'abnormal lateral pallium morphology', 0.4166666666666667, 8.02346099791745, 1.8284170063561187, 'HP:0002060', 'Abnormal cerebral morphology'),
(178944, 'HP:0000460', 'Narrow nose', 'XPO:0128502', 'decreased size of the anatomical line', 0.41025641025641024, 5.653868323764771, 1.5230022070142124, 'UPHENO:0012541', 'decreased size of the anatomical entity in the independent continuant'),
(178945, 'HP:0000460', 'Narrow nose', 'XPO:0128846', 'decreased size of the choana', 0.49230769230769234, 9.601025046317446, 2.1740879661000143, 'UPHENO:0021517', 'abnormal nose morphology'),
(178946, 'HP:0000460', 'Narrow nose', 'XPO:0128841', 'decreased size of the craniofacial region', 0.4528301886792453, 5.653868323764771, 1.6000757044021416, 'UPHENO:0012541', 'decreased size of the anatomical entity in the independent continuant'),
(178947, 'HP:0000460', 'Narrow nose', 'XPO:0130324', 'increased size of the choana', 0.44776119402985076, 9.601025046317446, 2.073394906584272, 'UPHENO:0021517', 'abnormal nose morphology'),
(178948, 'HP:0000460', 'Narrow nose', 'XPO:0141839', 'edematous pharyngeal region', 0.44680851063829785, 4.5318002188002176, 1.422971154406314, 'UPHENO:0087907', 'abnormal head morphology'),
(178949, 'HP:0000460', 'Narrow nose', 'XPO:0129920', 'increased size of the Jacobsons organ', 0.45161290322580644, 9.467216006125252, 2.0677323100421026, 'UPHENO:0087950', 'abnormal nose morphology'),
(178950, 'HP:0000460', 'Narrow nose', 'XPO:0141835', 'edematous head', 0.4375, 4.5318002188002176, 1.4080705222839853, 'UPHENO:0087907', 'abnormal head morphology'),
(178951, 'HP:0000460', 'Narrow nose', 'XPO:0131600', 'decreased size of the intercanthal region', 0.48, 5.653868323764771, 1.6473787650103693, 'UPHENO:0012541', 'decreased size of the anatomical entity in the independent continuant'),
(178952, 'HP:0000460', 'Narrow nose', 'XPO:0141298', 'abnormal intercanthal region morphology', 0.4375, 4.5318002188002176, 1.4080705222839853, 'UPHENO:0087907', 'abnormal head morphology'),
(178953, 'HP:0000460', 'Narrow nose', 'XPO:0102734', 'abnormal craniofacial region morphology', 0.42857142857142855, 4.5318002188002176, 1.3936283915633758, 'UPHENO:0087907', 'abnormal head morphology'),
(178954, 'HP:0000460', 'Narrow nose', 'XPO:0131462', 'increased size of the cilium in olfactory pit', 0.4117647058823529, 9.467216006125252, 1.9744025461609567, 'UPHENO:0087950', 'abnormal nose morphology'),
(178955, 'HP:0000460', 'Narrow nose', 'XPO:0102226', 'abnormal Jacobsons organ morphology', 0.48214285714285715, 9.467216006125252, 2.1364808855643473, 'UPHENO:0087950', 'abnormal nose morphology'),
(178956, 'HP:0000460', 'Narrow nose', 'XPO:0130934', 'increased size of the nostril', 0.47619047619047616, 9.601025046317446, 2.1382040802324256, 'UPHENO:0021517', 'abnormal nose morphology'),
(178957, 'HP:0000460', 'Narrow nose', 'XPO:0127898', 'abnormally localised nostril', 0.5087719298245614, 9.601025046317446, 2.210142991100095, 'UPHENO:0021517', 'abnormal nose morphology'),
(178958, 'HP:0000460', 'Narrow nose', 'XPO:0140335', 'abnormally necrotic pharyngeal region', 0.4375, 4.5318002188002176, 1.4080705222839853, 'UPHENO:0087907', 'abnormal head morphology'),
(178959, 'HP:0000460', 'Narrow nose', 'XPO:0102572', 'abnormal hatching gland primordium morphology', 0.4117647058823529, 4.5318002188002176, 1.3660290568695288, 'UPHENO:0087907', 'abnormal head morphology'),
(178960, 'HP:0000460', 'Narrow nose', 'XPO:0100420', 'abnormal choana', 0.5918367346938775, 9.601025046317446, 2.3837448087256847, 'UPHENO:0021517', 'abnormal nose morphology'),
(178961, 'HP:0000460', 'Narrow nose', 'XPO:0141339', 'decreased pigmentation in the head', 0.42857142857142855, 4.5318002188002176, 1.3936283915633758, 'UPHENO:0087907', 'abnormal head morphology'),
(178962, 'HP:0000460', 'Narrow nose', 'XPO:0126871', 'abnormally localised choana', 0.5178571428571429, 9.601025046317446, 2.2297890929381237, 'UPHENO:0021517', 'abnormal nose morphology'),
(178963, 'HP:0000460', 'Narrow nose', 'XPO:0102082', 'abnormal circumpharyngeal ridge morphology', 0.42, 4.5318002188002176, 1.3796217205799897, 'UPHENO:0087907', 'abnormal head morphology'),
(178964, 'HP:0000460', 'Narrow nose', 'XPO:0102538', 'abnormal lateral nasal prominence morphology', 0.42857142857142855, 4.5318002188002176, 1.3936283915633758, 'UPHENO:0087907', 'abnormal head morphology'),
(178965, 'HP:0000460', 'Narrow nose', 'XPO:0103101', 'abnormal medial nasal prominence morphology', 0.42857142857142855, 4.5318002188002176, 1.3936283915633758, 'UPHENO:0087907', 'abnormal head morphology'),
(178966, 'HP:0000460', 'Narrow nose', 'XPO:0129227', 'decreased size of the circumpharyngeal ridge', 0.4528301886792453, 5.653868323764771, 1.6000757044021416, 'UPHENO:0012541', 'decreased size of the anatomical entity in the independent continuant'),
(178967, 'HP:0000460', 'Narrow nose', 'XPO:0103115', 'abnormal nostril morphology', 0.5272727272727272, 9.601025046317446, 2.2499685910664535, 'UPHENO:0021517', 'abnormal nose morphology'),
(178968, 'HP:0000460', 'Narrow nose', 'XPO:0128599', 'decreased size of the olfactory pit', 0.5357142857142857, 9.467216006125252, 2.2520485919322972, 'UPHENO:0087950', 'abnormal nose morphology'),
(178969, 'HP:0000460', 'Narrow nose', 'XPO:0103707', 'increased pigmentation in the head', 0.42857142857142855, 4.5318002188002176, 1.3936283915633758, 'UPHENO:0087907', 'abnormal head morphology'),
(178970, 'HP:0000460', 'Narrow nose', 'XPO:0128817', 'decreased size of the hatching gland primordium', 0.43636363636363634, 5.653868323764771, 1.570714022754993, 'UPHENO:0012541', 'decreased size of the anatomical entity in the independent continuant'),
(178971, 'HP:0000460', 'Narrow nose', 'XPO:0133370', 'olfactory pit fused with brain', 0.47368421052631576, 9.467216006125252, 2.117656898495018, 'UPHENO:0087950', 'abnormal nose morphology'),
(178972, 'HP:0000460', 'Narrow nose', 'XPO:0101634', 'abnormal head morphology', 0.45652173913043476, 4.5318002188002176, 1.4383550734357495, 'UPHENO:0087907', 'abnormal head morphology'),
(178973, 'HP:0000460', 'Narrow nose', 'XPO:0102804', 'abnormal pharyngeal pouch morphology', 0.42857142857142855, 4.5318002188002176, 1.3936283915633758, 'UPHENO:0087907', 'abnormal head morphology'),
(178974, 'HP:0000460', 'Narrow nose', 'XPO:0102966', 'abnormal olfactory pit morphology', 0.5, 9.467216006125252, 2.1756856397610904, 'UPHENO:0087950', 'abnormal nose morphology'),
(178975, 'HP:0000460', 'Narrow nose', 'XPO:0128795', 'decreased size of the pharyngeal pouch', 0.4528301886792453, 5.653868323764771, 1.6000757044021416, 'UPHENO:0012541', 'decreased size of the anatomical entity in the independent continuant'),
(178976, 'HP:0000460', 'Narrow nose', 'XPO:0128256', 'decreased size of the cranial placode', 0.4067796610169492, 5.653868323764771, 1.5165350771332327, 'UPHENO:0012541', 'decreased size of the anatomical entity in the independent continuant'),
(178977, 'HP:0000460', 'Narrow nose', 'XPO:0142059', 'abnormal nasal region morphology', 0.44680851063829785, 4.5318002188002176, 1.422971154406314, 'UPHENO:0087907', 'abnormal head morphology'),
(178978, 'HP:0000460', 'Narrow nose', 'XPO:0128582', 'decreased size of the head region', 0.48, 5.653868323764771, 1.6473787650103693, 'UPHENO:0012541', 'decreased size of the anatomical entity in the independent continuant'),
(178979, 'HP:0000460', 'Narrow nose', 'XPO:0129164', 'decreased size of the medial nasal prominence', 0.46153846153846156, 5.653868323764771, 1.6153877825127416, 'UPHENO:0012541', 'decreased size of the anatomical entity in the independent continuant'),
(178980, 'HP:0000460', 'Narrow nose', 'XPO:0128568', 'decreased size of the optic disc', 0.4090909090909091, 5.788671267106304, 1.5388608745071604, 'UPHENO:0087472', 'abnormal face morphology'),
(178981, 'HP:0000460', 'Narrow nose', 'XPO:0140914', 'abnormally necrotic intercanthal region', 0.4117647058823529, 4.5318002188002176, 1.3660290568695288, 'UPHENO:0087907', 'abnormal head morphology'),
(178982, 'HP:0000460', 'Narrow nose', 'XPO:0115526', 'abnormally incomplete structure of head', 0.44680851063829785, 4.5318002188002176, 1.422971154406314, 'UPHENO:0087907', 'abnormal head morphology'),
(178983, 'HP:0000460', 'Narrow nose', 'XPO:0142038', 'decreased size of the nasal region', 0.4528301886792453, 5.653868323764771, 1.6000757044021416, 'UPHENO:0012541', 'decreased size of the anatomical entity in the independent continuant'),
(178984, 'HP:0000460', 'Narrow nose', 'XPO:0102259', 'abnormal pharyngeal region morphology', 0.4666666666666667, 4.5318002188002176, 1.4542489821577214, 'UPHENO:0087907', 'abnormal head morphology'),
(178985, 'HP:0000460', 'Narrow nose', 'XPO:0103358', 'decreased size of the pharyngeal region', 0.5106382978723404, 5.653868323764771, 1.699141458867267, 'UPHENO:0012541', 'decreased size of the anatomical entity in the independent continuant'),
(178986, 'HP:0000460', 'Narrow nose', 'XPO:0130787', 'increased size of the lateral nasal prominence', 0.4074074074074074, 4.6864066944795475, 1.3817658272857345, 'UPHENO:0075195', 'abnormal size of anatomical entity'),
(178987, 'HP:0000460', 'Narrow nose', 'XPO:0133429', 'abnormal cilium morphology in the olfactory pit', 0.43548387096774194, 9.467216006125252, 2.030472820215821, 'UPHENO:0087950', 'abnormal nose morphology'),
(178988, 'HP:0000460', 'Narrow nose', 'XPO:0125246', 'absent choana', 0.47540983606557374, 9.601025046317446, 2.136450735058322, 'UPHENO:0021517', 'abnormal nose morphology'),
(178989, 'HP:0000460', 'Narrow nose', 'XPO:0139715', 'abnormally necrotic head', 0.4117647058823529, 4.5318002188002176, 1.3660290568695288, 'UPHENO:0087907', 'abnormal head morphology'),
(178990, 'HP:0000460', 'Narrow nose', 'XPO:0103739', 'increased size of the pharyngeal region', 0.4489795918367347, 4.6864066944795475, 1.4505519517991654, 'UPHENO:0075195', 'abnormal size of anatomical entity'),
(178991, 'HP:0000460', 'Narrow nose', 'XPO:0101483', 'abnormal nostril', 0.6170212765957447, 9.601025046317446, 2.433934413805456, 'UPHENO:0021517', 'abnormal nose morphology'),
(178992, 'HP:0000460', 'Narrow nose', 'XPO:0128102', 'decreased size of the portion of organism substance', 0.41025641025641024, 5.653868323764771, 1.5230022070142124, 'UPHENO:0012541', 'decreased size of the anatomical entity in the independent continuant'),
(178993, 'HP:0000460', 'Narrow nose', 'XPO:0130079', 'increased size of the olfactory pit', 0.4827586206896552, 9.467216006125252, 2.1378447419978963, 'UPHENO:0087950', 'abnormal nose morphology'),
(178994, 'HP:0000460', 'Narrow nose', 'XPO:0102052', 'abnormal choana morphology', 0.46774193548387094, 9.601025046317446, 2.1191512541094477, 'UPHENO:0021517', 'abnormal nose morphology'),
(178995, 'HP:0000460', 'Narrow nose', 'XPO:0128007', 'decreased size of the anatomical structure', 0.41025641025641024, 5.653868323764771, 1.5230022070142124, 'UPHENO:0012541', 'decreased size of the anatomical entity in the independent continuant'),
(178996, 'HP:0000460', 'Narrow nose', 'XPO:0103827', 'decreased width of the head', 0.48148148148148145, 10.712203956541591, 2.2710631499206344, 'UPHENO:0034770', 'decreased width of the anatomical entity in independent continuant'),
(178997, 'HP:0000460', 'Narrow nose', 'XPO:0130640', 'increased size of the medial nasal prominence', 0.4074074074074074, 4.6864066944795475, 1.3817658272857345, 'UPHENO:0075195', 'abnormal size of anatomical entity'),
(178998, 'HP:0000460', 'Narrow nose', 'XPO:0140223', 'abnormally necrotic head region', 0.4117647058823529, 4.5318002188002176, 1.3660290568695288, 'UPHENO:0087907', 'abnormal head morphology'),
(178999, 'HP:0000460', 'Narrow nose', 'XPO:0130062', 'increased size of the head region', 0.4230769230769231, 4.6864066944795475, 1.4080875415213008, 'UPHENO:0075195', 'abnormal size of anatomical entity'),
(179000, 'HP:0000460', 'Narrow nose', 'XPO:0140593', 'abnormally necrotic Jacobsons organ', 0.4426229508196721, 9.467216006125252, 2.0470483835704494, 'UPHENO:0087950', 'abnormal nose morphology'),
(179001, 'HP:0000460', 'Narrow nose', 'XPO:0131491', 'decreased size of the cilium in the olfactory pit', 0.45454545454545453, 9.467216006125252, 2.0744348634710623, 'UPHENO:0087950', 'abnormal nose morphology'),
(179002, 'HP:0000460', 'Narrow nose', 'XPO:0103342', 'decreased size of the head', 0.46153846153846156, 5.653868323764771, 1.6153877825127416, 'UPHENO:0012541', 'decreased size of the anatomical entity in the independent continuant'),
(179003, 'HP:0000460', 'Narrow nose', 'XPO:0126234', 'absent nostril', 0.46774193548387094, 9.601025046317446, 2.1191512541094477, 'UPHENO:0021517', 'abnormal nose morphology'),
(179004, 'HP:0000460', 'Narrow nose', 'XPO:0131638', 'increased size of the intercanthal region', 0.4230769230769231, 4.6864066944795475, 1.4080875415213008, 'UPHENO:0075195', 'abnormal size of anatomical entity'),
(179005, 'HP:0000460', 'Narrow nose', 'XPO:0128440', 'decreased size of the Jacobsons organ', 0.4918032786885246, 9.467216006125252, 2.1577784575495413, 'UPHENO:0087950', 'abnormal nose morphology'),
(179006, 'HP:0000460', 'Narrow nose', 'XPO:0129460', 'decreased size of the nostril', 0.5161290322580645, 9.601025046317446, 2.2260655349385523, 'UPHENO:0021517', 'abnormal nose morphology'),
(179007, 'HP:0000460', 'Narrow nose', 'XPO:0101334', 'abnormal olfactory pit', 0.40425531914893614, 9.116652820832241, 1.9197539935251045, 'HP:0000366', 'Abnormality of the nose'),
(179008, 'HP:0000460', 'Narrow nose', 'XPO:0103435', 'decreased size of the head mesenchyme', 0.4067796610169492, 5.653868323764771, 1.5165350771332327, 'UPHENO:0012541', 'decreased size of the anatomical entity in the independent continuant'),
(179009, 'HP:0000460', 'Narrow nose', 'XPO:0129311', 'decreased size of the lateral nasal prominence', 0.46153846153846156, 5.653868323764771, 1.6153877825127416, 'UPHENO:0012541', 'decreased size of the anatomical entity in the independent continuant'),
(179010, 'HP:0000460', 'Narrow nose', 'XPO:0103826', 'decreased width of the craniofacial region', 0.48148148148148145, 10.712203956541591, 2.2710631499206344, 'UPHENO:0034770', 'decreased width of the anatomical entity in independent continuant'),
(179011, 'HP:0033072', 'Abnormal macroscopic urine appearance', 'XPO:0100069', 'abnormal urinary system', 0.5, 6.355235291121788, 1.7825873458433654, 'HP:0000079', 'Abnormality of the urinary system'),
(179012, 'HP:0033072', 'Abnormal macroscopic urine appearance', 'XPO:0101579', 'abnormal urethra', 0.40540540540540543, 6.355235291121788, 1.6051313776896794, 'HP:0000079', 'Abnormality of the urinary system'),
(179013, 'HP:0033072', 'Abnormal macroscopic urine appearance', 'XPO:0124921', 'absent urinary system', 0.41025641025641024, 6.355235291121788, 1.61470617044417, 'HP:0000079', 'Abnormality of the urinary system'),
(179014, 'HP:0033072', 'Abnormal macroscopic urine appearance', 'XPO:0101212', 'abnormal glomeral mesenchyme', 0.40625, 5.4478002382576385, 1.4876722914648124, 'HP:0000119', 'Abnormality of the genitourinary system'),
(179015, 'HP:0033072', 'Abnormal macroscopic urine appearance', 'XPO:0100501', 'abnormal urogenital system', 0.4482758620689655, 5.4478002382576385, 1.562727534851952, 'HP:0000119', 'Abnormality of the genitourinary system'),
(179016, 'HP:0033072', 'Abnormal macroscopic urine appearance', 'XPO:0100085', 'abnormal mesonephric sinus', 0.42857142857142855, 6.355235291121788, 1.6503551943819923, 'HP:0000079', 'Abnormality of the urinary system'),
(179017, 'HP:0033072', 'Abnormal macroscopic urine appearance', 'XPO:0126535', 'abnormally localised urinary system', 0.42105263157894735, 6.355235291121788, 1.6358143365401303, 'HP:0000079', 'Abnormality of the urinary system'),
(179018, 'HP:0033072', 'Abnormal macroscopic urine appearance', 'XPO:0100761', 'abnormal ureter', 0.40540540540540543, 6.355235291121788, 1.6051313776896794, 'HP:0000079', 'Abnormality of the urinary system'),
(179019, 'HP:0033072', 'Abnormal macroscopic urine appearance', 'XPO:0101701', 'abnormal urinary system morphology', 0.42105263157894735, 6.355235291121788, 1.6358143365401303, 'HP:0000079', 'Abnormality of the urinary system'),
(179020, 'HP:0033072', 'Abnormal macroscopic urine appearance', 'XPO:0100120', 'abnormal genital system', 0.40625, 5.4478002382576385, 1.4876722914648124, 'HP:0000119', 'Abnormality of the genitourinary system'),
(179021, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0131666', 'abnormal adherens junction', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(179022, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0141798', 'abnormal lipid metabolic process', 0.4782608695652174, 4.758907843651163, 1.508641575552437, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(179023, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0101109', 'abnormal egg cell-free extract', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(179024, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0107253', 'abnormal enteric nervous system', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(179025, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0131730', 'abnormal regulation of protein folding', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(179026, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0100533', 'abnormal melanoblast', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(179027, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0141738', 'abnormal carbon dioxide homeostasis', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(179028, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0100585', 'abnormal elastica externa', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(179029, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0100917', 'abnormal stage III oocyte', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(179030, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0101157', 'abnormal female organism', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(179031, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0141782', 'abnormal methylation', 0.5238095238095238, 4.758907843651163, 1.5788480773767701, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(179032, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0100546', 'abnormal whole organism', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(179033, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0100423', 'abnormal process', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(179034, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0100902', 'abnormal spermatocyte', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(179035, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0100285', 'abnormal progenitor cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(179036, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0141892', 'abnormal inositol metabolic process', 0.4782608695652174, 4.758907843651163, 1.508641575552437, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(179037, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0141880', 'abnormal ethanolamine metabolic process', 0.44, 4.758907843651163, 1.447038165082909, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(179038, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0141265', 'abnormal escape behavior', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(179039, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0100062', 'abnormal anatomical space', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(179040, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0100976', 'abnormal multiciliated cell', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(179041, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0141499', 'abnormal tadpole', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(179042, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0141778', 'abnormal biosynthetic process', 0.5238095238095238, 4.758907843651163, 1.5788480773767701, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(179043, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0100704', 'abnormal Merkel cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(179044, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0100032', 'abnormal nervous system', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(179045, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0100574', 'abnormal gastrula cell', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(179046, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0100307', 'abnormal blastomere', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(179047, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0141263', 'abnormal visually guided collision avoidance behavior', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(179048, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0101237', 'abnormal mucus secreting cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(179049, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0100377', 'abnormal connective tissue', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(179050, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0141784', 'abnormal cellular hormone metabolic process', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(179051, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0141850', 'abnormal galactose metabolic process', 0.4230769230769231, 4.758907843651163, 1.418937661667548, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(179052, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0141852', 'abnormal glucose metabolic process', 0.4230769230769231, 4.758907843651163, 1.418937661667548, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(179053, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0107260', 'abnormal anterior-posterior axis', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(179054, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0141872', 'abnormal cholesterol metabolic process', 0.4074074074074074, 4.758907843651163, 1.392413123563799, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(179055, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0101241', 'abnormal nucleate erythrocyte', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(179056, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0141745', 'abnormal creatinine homeostasis', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(179057, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0100386', 'abnormal limb', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(179058, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0100721', 'abnormal centromere', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(179059, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0101480', 'abnormal stage V oocyte', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(179060, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0141910', 'abnormal D-ribose metabolic process', 0.4230769230769231, 4.758907843651163, 1.418937661667548, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(179061, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0115512', 'abnormally semi-erect whole organism', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(179062, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0107262', 'abnormal left-right axis', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(179063, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0141754', 'abnormal homeostatic process', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(179064, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0101461', 'abnormal sperm entry point', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(179065, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0100715', 'abnormal ciliated cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(179066, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0100317', 'abnormal respiratory system', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(179067, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0100894', 'abnormal nucleus', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(179068, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0101071', 'abnormal endoplasmic reticulum', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(179069, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0100802', 'abnormal exocrine cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(179070, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0141790', 'abnormal cellular metabolic process', 0.5, 4.758907843651163, 1.5425478669479211, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(179071, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0101326', 'abnormal cementoblast', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(179072, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0100258', 'abnormal organ part', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(179073, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0100232', 'abnormal lymphatic system', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(179074, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0141771', 'abnormal urea homeostasis', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(179075, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0133403', 'abnormal developmental process', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(179076, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0101472', 'abnormal zygote cortex', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(179077, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0116434', 'abnormal biological process', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(179078, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0141775', 'abnormal nitrogen compound metabolic process', 0.5238095238095238, 4.758907843651163, 1.5788480773767701, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(179079, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0141743', 'abnormal chemical homeostasis within a tissue', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(179080, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0101297', 'abnormal barrier cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(179081, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0101240', 'abnormal ciliated non-epidermal cell', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(179082, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0100899', 'abnormal secondary spermatogonium', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(179083, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0141883', 'abnormal glycerol metabolic process', 0.4230769230769231, 4.758907843651163, 1.418937661667548, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(179084, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0131691', 'abnormal molecular function', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(179085, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0100674', 'abnormal secondary oogonium', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(179086, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0101220', 'abnormal centriole', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(179087, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0141600', 'absent metamorphosis', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(179088, 'HP:0033978', 'Reduced beta-hexosaminidase 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'),
(179089, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0141908', 'abnormal pyridine metabolic process', 0.4230769230769231, 4.758907843651163, 1.418937661667548, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(179090, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0141854', 'abnormal glutathione metabolic process', 0.4230769230769231, 4.758907843651163, 1.418937661667548, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(179091, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0141272', 'absent surface breathing', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(179092, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0131745', 'abnormal axis elongation', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(179093, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0100239', 'abnormal acellular anatomical structure', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(179094, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0141907', 'abnormal putrescine metabolic process', 0.4782608695652174, 4.758907843651163, 1.508641575552437, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(179095, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0141791', 'abnormal primary metabolic process', 0.5238095238095238, 4.758907843651163, 1.5788480773767701, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(179096, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0141864', 'abnormal 5-methylcytosine metabolic process', 0.4230769230769231, 4.758907843651163, 1.418937661667548, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(179097, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0115505', 'dead whole organism', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(179098, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0141877', 'abnormal 2-deoxyribose 1-phosphate metabolic process', 0.4583333333333333, 4.758907843651163, 1.4768771428276568, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(179099, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0116494', 'absent biological process', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(179100, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0101535', 'abnormal absorptive cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(179101, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0107312', 'abnormal filopodium', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(179102, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0141789', 'abnormal hormone catabolic process', 0.44, 4.758907843651163, 1.447038165082909, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(179103, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0100308', 'abnormal early embryonic cell', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(179104, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0101228', 'abnormal mesenchymal stem cell', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(179105, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0141809', 'abnormal catalytic activity', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(179106, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0100754', 'abnormal electrically active cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(179107, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0141264', 'abnormal schooling behavior', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(179108, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0100081', 'abnormal anatomical entity in vitro', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(179109, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0100031', 'abnormal central nervous system', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(179110, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0141787', 'abnormal hormone metabolic process', 0.5238095238095238, 4.758907843651163, 1.5788480773767701, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(179111, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0107284', 'abnormal migrating myoblast', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(179112, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0100545', 'abnormal male organism', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(179113, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0107270', 'abnormal proximal-distal axis', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(179114, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0141881', 'abnormal fructose metabolic process', 0.4230769230769231, 4.758907843651163, 1.418937661667548, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(179115, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0100225', 'abnormal endocrine system', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(179116, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0141783', 'abnormal collagen metabolic process', 0.5238095238095238, 4.758907843651163, 1.5788480773767701, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(179117, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0100969', 'abnormal disaggregated/reaggregated ectoderm treated with activin', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(179118, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0101333', 'abnormal barrier epithelial cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(179119, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0100172', 'abnormal stem cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(179120, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0100907', 'abnormal cytoplasm', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(179121, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0101448', 'abnormal myelin accumulating cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(179122, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0100026', 'abnormal germ cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(179123, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0141796', 'abnormal demethylation', 0.5238095238095238, 4.758907843651163, 1.5788480773767701, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(179124, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0107259', 'abnormal animal-vegetal axis', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(179125, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0101110', 'abnormal cell-free extract', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(179126, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0100289', 'abnormal chondroblast', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(179127, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0101373', 'abnormal oxygen accumulating cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(179128, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0101409', 'abnormal perivitelline space', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(179129, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0100728', 'abnormal cell condensation', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(179130, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0141772', 'abnormal water homeostasis', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(179131, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0101513', 'abnormal basal body', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(179132, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0100501', 'abnormal urogenital system', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(179133, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0141866', 'abnormal dicarboxylic acid metabolic process', 0.4074074074074074, 4.758907843651163, 1.392413123563799, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(179134, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0101004', 'abnormal acid secreting cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(179135, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0101132', 'abnormal apoptotic cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(179136, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0141911', 'abnormal ribose phosphate metabolic process', 0.4583333333333333, 4.758907843651163, 1.4768771428276568, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(179137, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0128000', 'absent behavior', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(179138, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0100477', 'abnormal pericyte', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(179139, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0141777', 'abnormal catabolic process', 0.5238095238095238, 4.758907843651163, 1.5788480773767701, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(179140, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0131729', 'abnormal regulation of growth rate', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(179141, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0100337', 'abnormal zygote', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(179142, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0141770', 'abnormal urate homeostasis', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(179143, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0100392', 'abnormal cilium', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(179144, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0100429', 'abnormal spermatid', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(179145, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:00000000', 'Xenopus phenotype', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(179146, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0131677', 'abnormal actin filament', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(179147, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0141266', 'abnormal surface breathing', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(179148, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0141860', 'abnormal malate-aspartate shuttle', 0.5, 4.758907843651163, 1.5425478669479211, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(179149, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0100852', 'abnormal interdigital region', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(179150, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0101221', 'abnormal larval immune system', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(179151, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0100084', 'abnormal anatomical group', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(179152, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0100888', 'abnormal microtubule', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(179153, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0100653', 'abnormal myoblast', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(179154, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0141794', 'abnormal prosthetic group metabolic process', 0.5238095238095238, 4.758907843651163, 1.5788480773767701, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(179155, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0142057', 'abnormal desmosome', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(179156, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0141859', 'abnormal lactose catabolic process', 0.4230769230769231, 4.758907843651163, 1.418937661667548, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(179157, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0141900', 'abnormal mannose metabolic process', 0.4230769230769231, 4.758907843651163, 1.418937661667548, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(179158, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0141904', 'abnormal glucosamine metabolic process', 0.5238095238095238, 4.758907843651163, 1.5788480773767701, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(179159, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0131667', 'abnormal actin cytoskeleton', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(179160, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0141776', 'abnormal metabolic process', 0.5789473684210527, 4.758907843651163, 1.6598666129060333, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(179161, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0131694', 'abnormal RNA polymerase II activity', 0.4583333333333333, 4.758907843651163, 1.4768771428276568, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(179162, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0100599', 'abnormal adult immune system', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(179163, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0100581', 'abnormal immune system', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(179164, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0100025', 'abnormal oocyte', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(179165, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0141797', 'abnormal hydrogen metabolic process', 0.5238095238095238, 4.758907843651163, 1.5788480773767701, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(179166, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0115509', 'abnormally semi-viable whole organism', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(179167, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0141898', 'abnormal maltose metabolic process', 0.4583333333333333, 4.758907843651163, 1.4768771428276568, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(179168, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0101569', 'abnormal activin-induced ectoderm', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(179169, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0101141', 'abnormal Keller explant', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(179170, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0141792', 'abnormal small molecule metabolic process', 0.5238095238095238, 4.758907843651163, 1.5788480773767701, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(179171, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0100006', 'abnormal anatomical structure', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(179172, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0100437', 'abnormal proepicardium', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(179173, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0100108', 'abnormal cell part', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(179174, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0100010', 'abnormal multicellular anatomical structure', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(179175, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0100344', 'abnormal portion of organism substance', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(179176, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0100549', 'abnormal mitotic cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(179177, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0141748', 'abnormal gas homeostasis', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(179178, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0100626', 'abnormal primordial germ cell', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(179179, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0141276', 'decreased surface breathing', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(179180, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0101113', 'abnormal stage IV oocyte', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(179181, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0131469', 'abnormal heart process', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(179182, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0100176', 'abnormal stage VI oocyte', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(179183, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0141315', 'abnormal anatomical region', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(179184, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0101498', 'abnormal stage II oocyte', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(179185, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0100573', 'abnormal extraembryonic structure', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(179186, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0100515', 'abnormal somatic stem cell', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(179187, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0101264', 'abnormal mitotic spindle', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(179188, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0101061', 'abnormal plasma membrane', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(179189, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0141903', 'abnormal inositol phosphate metabolic process', 0.4230769230769231, 4.758907843651163, 1.418937661667548, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(179190, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0131675', 'abnormal spindle microtubule', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(179191, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0100004', 'abnormal cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(179192, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0101547', 'abnormal lampbrush chromosome', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(179193, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0141767', 'abnormal temperature homeostasis', 0.44, 4.758907843651163, 1.447038165082909, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(179194, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0101467', 'abnormal alkali secreting cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(179195, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0141781', 'abnormal secondary metabolic process', 0.5238095238095238, 4.758907843651163, 1.5788480773767701, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(179196, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0141884', 'abnormal phosphagen metabolic process', 0.4230769230769231, 4.758907843651163, 1.418937661667548, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(179197, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0100724', 'abnormal kinetochore', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(179198, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0115508', 'abnormally peramorphic growth of whole organism', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(179199, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0101468', 'abnormal stage I oocyte', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(179200, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0141271', 'increased surface breathing', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(179201, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0141786', 'abnormal pigment metabolic process', 0.5238095238095238, 4.758907843651163, 1.5788480773767701, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(179202, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0100481', 'abnormal anatomical line', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(179203, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0101366', 'abnormal morula cell', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(179204, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0141795', 'abnormal glycosylation', 0.4782608695652174, 4.758907843651163, 1.508641575552437, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(179205, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0141788', 'abnormal hormone biosynthetic process', 0.44, 4.758907843651163, 1.447038165082909, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(179206, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0100791', 'abnormal multiciliated cell precursor', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(179207, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0107258', 'abnormal anatomical axis', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(179208, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0100956', 'abnormal centrosome', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(179209, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0131685', 'abnormal cortical actin cytoskeleton', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(179210, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0100638', 'abnormal polar body', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(179211, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0101435', 'abnormal paracrine cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(179212, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0131723', 'abnormal pathway-restricted SMAD protein phosphorylation', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(179213, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0107261', 'abnormal dorsal-ventral axis', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(179214, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0100274', 'abnormal sensory system', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(179215, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0100202', 'abnormal embryo', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(179216, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0141267', 'abnormal resting posture', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(179217, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0100691', 'abnormal keratin accumulating cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(179218, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0133388', 'absent insulin receptor signaling pathway', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(179219, 'HP:0033978', 'Reduced beta-hexosaminidase activity', 'XPO:0100372', 'abnormal hematological system', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(179220, 'HP:0000183', 'Difficulty in tongue movements', 'XPO:0101567', 'abnormal tongue', 0.7391304347826086, 10.93592543835056, 2.8430749768513386, 'HP:0000157', 'Abnormality of the tongue'),
(179221, 'HP:0000183', 'Difficulty in tongue movements', 'XPO:0141009', 'abnormally necrotic oral epithelium', 0.410958904109589, 7.312692920701687, 1.733555960672027, 'UPHENO:0076800', 'abnormal mouth morphology'),
(179222, 'HP:0000183', 'Difficulty in tongue movements', 'XPO:0103138', 'abnormal upper jaw morphology', 0.40540540540540543, 7.312692920701687, 1.7218029033900208, 'UPHENO:0076800', 'abnormal mouth morphology'),
(179223, 'HP:0000183', 'Difficulty in tongue movements', 'XPO:0115558', 'abnormally incomplete structure of mouth', 0.5172413793103449, 7.312692920701687, 1.9448463622550587, 'UPHENO:0076800', 'abnormal mouth morphology'),
(179224, 'HP:0000183', 'Difficulty in tongue movements', 'XPO:0126089', 'absent tongue', 0.576271186440678, 10.93592543835056, 2.510390154375425, 'HP:0000157', 'Abnormality of the tongue'),
(179225, 'HP:0000183', 'Difficulty in tongue movements', 'XPO:0100591', 'abnormal pharyngeal arch', 0.40425531914893614, 5.05060299610679, 1.4288922723864537, 'HP:0025031', 'Abnormality of the digestive system'),
(179226, 'HP:0000183', 'Difficulty in tongue movements', 'XPO:0127750', 'abnormally localised tongue', 0.5964912280701754, 10.93592543835056, 2.55405238685615, 'HP:0000157', 'Abnormality of the tongue'),
(179227, 'HP:0000183', 'Difficulty in tongue movements', 'XPO:0100647', 'abnormal mouth', 0.45098039215686275, 7.0866363731414825, 1.7877175533714584, 'HP:0000153', 'Abnormality of the mouth'),
(179228, 'HP:0000183', 'Difficulty in tongue movements', 'XPO:0100027', 'abnormal lower jaw', 0.42592592592592593, 7.0866363731414825, 1.7373491758799184, 'HP:0000153', 'Abnormality of the mouth'),
(179229, 'HP:0000183', 'Difficulty in tongue movements', 'XPO:0103735', 'increased size of the mouth', 0.48484848484848486, 7.884497199543557, 1.9551947527013303, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(179230, 'HP:0000183', 'Difficulty in tongue movements', 'XPO:0102279', 'abnormal mouth morphology', 0.5263157894736842, 7.312692920701687, 1.96183224250641, 'UPHENO:0076800', 'abnormal mouth morphology'),
(179231, 'HP:0000183', 'Difficulty in tongue movements', 'XPO:0141311', 'abnormal roof of mouth morphology', 0.5, 7.312692920701687, 1.9121575406725366, 'UPHENO:0076800', 'abnormal mouth morphology'),
(179232, 'HP:0000183', 'Difficulty in tongue movements', 'XPO:0102960', 'abnormal oral epithelium morphology', 0.45454545454545453, 7.312692920701687, 1.8231706797751206, 'UPHENO:0076800', 'abnormal mouth morphology'),
(179233, 'HP:0000183', 'Difficulty in tongue movements', 'XPO:0140626', 'abnormally necrotic tongue', 0.5666666666666667, 10.93592543835056, 2.489382336055536, 'HP:0000157', 'Abnormality of the tongue'),
(179234, 'HP:0000183', 'Difficulty in tongue movements', 'XPO:0130628', 'increased size of the oral cavity', 0.5161290322580645, 7.884497199543557, 2.017279829235854, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(179235, 'HP:0000183', 'Difficulty in tongue movements', 'XPO:0129585', 'increased size of the tongue', 0.4657534246575342, 10.93592543835056, 2.2568661291071783, 'HP:0000157', 'Abnormality of the tongue'),
(179236, 'HP:0000183', 'Difficulty in tongue movements', 'XPO:0115393', 'abnormally decreased volume of oral cavity', 0.5, 7.884497199543557, 1.9855096574360394, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(179237, 'HP:0000183', 'Difficulty in tongue movements', 'XPO:0101659', 'abnormal lower jaw morphology', 0.4166666666666667, 7.312692920701687, 1.7455530308832508, 'UPHENO:0076800', 'abnormal mouth morphology'),
(179238, 'HP:0000183', 'Difficulty in tongue movements', 'XPO:0103199', 'abnormal tongue morphology', 0.6181818181818182, 10.93592543835056, 2.600075051028402, 'HP:0000157', 'Abnormality of the tongue'),
(179239, 'HP:0000183', 'Difficulty in tongue movements', 'XPO:0131573', 'decreased size of the roof of mouth', 0.44776119402985076, 7.312692920701687, 1.8095137782694621, 'UPHENO:0076800', 'abnormal mouth morphology'),
(179240, 'HP:0000183', 'Difficulty in tongue movements', 'XPO:0101816', 'abnormal tooth morphology', 0.42105263157894735, 7.884497199543557, 1.8220286206711067, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(179241, 'HP:0000183', 'Difficulty in tongue movements', 'XPO:0101464', 'abnormal oral cavity', 0.4423076923076923, 7.0866363731414825, 1.7704445149249843, 'HP:0000153', 'Abnormality of the mouth'),
(179242, 'HP:0000183', 'Difficulty in tongue movements', 'XPO:0129152', 'decreased size of the oral cavity', 0.5161290322580645, 7.884497199543557, 2.017279829235854, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(179243, 'HP:0000183', 'Difficulty in tongue movements', 'XPO:0131651', 'abnormal roof of mouth', 0.4339622641509434, 7.0866363731414825, 1.7536626715827954, 'HP:0000153', 'Abnormality of the mouth'),
(179244, 'HP:0000183', 'Difficulty in tongue movements', 'XPO:0101328', 'abnormal oral epithelium', 0.41818181818181815, 7.0866363731414825, 1.721482641014341, 'HP:0000153', 'Abnormality of the mouth'),
(179245, 'HP:0000183', 'Difficulty in tongue movements', 'XPO:0102204', 'abnormal branchial arch morphology', 0.4067796610169492, 5.725717590856133, 1.5261407080237526, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(179246, 'HP:0000183', 'Difficulty in tongue movements', 'XPO:0103352', 'decreased size of the mouth', 0.48484848484848486, 7.884497199543557, 1.9551947527013303, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(179247, 'HP:0000183', 'Difficulty in tongue movements', 'XPO:0103828', 'decreased width of the mouth', 0.4507042253521127, 7.884497199543557, 1.885093154889482, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(179248, 'HP:0000183', 'Difficulty in tongue movements', 'XPO:0131611', 'increased size of the roof of mouth', 0.44776119402985076, 7.312692920701687, 1.8095137782694621, 'UPHENO:0076800', 'abnormal mouth morphology'),
(179249, 'HP:0000183', 'Difficulty in tongue movements', 'XPO:0140789', 'abnormally necrotic roof of mouth', 0.46153846153846156, 7.312692920701687, 1.8371415406342146, 'UPHENO:0076800', 'abnormal mouth morphology'),
(179250, 'HP:0000183', 'Difficulty in tongue movements', 'XPO:0141830', 'increased width of mouth', 0.4507042253521127, 7.884497199543557, 1.885093154889482, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(179251, 'HP:0000183', 'Difficulty in tongue movements', 'XPO:0103096', 'abnormal oral cavity morphology', 0.5614035087719298, 7.884497199543557, 2.103897429231332, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(179252, 'HP:0000183', 'Difficulty in tongue movements', 'XPO:0101506', 'abnormal upper jaw', 0.42592592592592593, 7.0866363731414825, 1.7373491758799184, 'HP:0000153', 'Abnormality of the mouth'),
(179253, 'HP:0000183', 'Difficulty in tongue movements', 'XPO:0102223', 'abnormal pharyngeal arch morphology', 0.42105263157894735, 5.725717590856133, 1.5526842754751673, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(179254, 'HP:0000183', 'Difficulty in tongue movements', 'XPO:0128105', 'decreased size of the tongue', 0.5, 10.93592543835056, 2.338367532954407, 'HP:0000157', 'Abnormality of the tongue'),
(179255, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0100477', 'abnormal pericyte', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(179256, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0141776', 'abnormal metabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(179257, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0101450', 'abnormal myeloid cell', 0.4642857142857143, 5.574066539846944, 1.6087136056268494, 'HP:0001871', 'Abnormality of blood and blood-forming tissues'),
(179258, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0101109', 'abnormal egg cell-free extract', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(179259, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0100386', 'abnormal limb', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(179260, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0101101', 'abnormal posterior foregut', 0.43333333333333335, 4.970960464763942, 1.4676794159707953, 'HP:0011793', 'Neoplasm by anatomical site'),
(179261, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0101132', 'abnormal apoptotic cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(179262, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0131667', 'abnormal actin cytoskeleton', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(179263, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0101435', 'abnormal paracrine cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(179264, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0100307', 'abnormal blastomere', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(179265, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0100721', 'abnormal centromere', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(179266, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0131666', 'abnormal adherens junction', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(179267, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0101113', 'abnormal stage IV oocyte', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(179268, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0100969', 'abnormal disaggregated/reaggregated ectoderm treated with activin', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(179269, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0107260', 'abnormal anterior-posterior axis', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(179270, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0100004', 'abnormal cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(179271, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0100062', 'abnormal anatomical space', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(179272, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0101237', 'abnormal mucus secreting cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(179273, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0100823', 'abnormal blood', 0.5, 5.574066539846944, 1.6694410052240456, 'HP:0001871', 'Abnormality of blood and blood-forming tissues'),
(179274, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0100728', 'abnormal cell condensation', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(179275, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0107258', 'abnormal anatomical axis', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(179276, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0101220', 'abnormal centriole', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(179277, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0101381', 'abnormal ventral foregut', 0.43333333333333335, 4.970960464763942, 1.4676794159707953, 'HP:0011793', 'Neoplasm by anatomical site'),
(179278, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0100621', 'abnormal peritoneum', 0.40625, 4.970960464763942, 1.4210744839065794, 'HP:0011793', 'Neoplasm by anatomical site'),
(179279, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0100735', 'abnormal hindgut', 0.4482758620689655, 4.970960464763942, 1.4927697704779535, 'HP:0011793', 'Neoplasm by anatomical site'),
(179280, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0100581', 'abnormal immune system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(179281, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0100715', 'abnormal ciliated cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(179282, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0101601', 'abnormal proctodeum', 0.41935483870967744, 4.970960464763942, 1.4438131194629262, 'HP:0011793', 'Neoplasm by anatomical site'),
(179283, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0100493', 'abnormal liver and biliary system', 0.48148148148148145, 4.970960464763942, 1.5470699431378068, 'HP:0011793', 'Neoplasm by anatomical site'),
(179284, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0101071', 'abnormal endoplasmic reticulum', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(179285, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0100032', 'abnormal nervous system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(179286, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0100429', 'abnormal spermatid', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(179287, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0101373', 'abnormal oxygen accumulating cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(179288, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0115508', 'abnormally peramorphic growth of whole organism', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(179289, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0101056', 'abnormal anterior ventral blood island', 0.43333333333333335, 5.574066539846944, 1.5541649957239663, 'HP:0001871', 'Abnormality of blood and blood-forming tissues'),
(179290, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0101468', 'abnormal stage I oocyte', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(179291, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0100890', 'abnormal pharyngeal cavity', 0.4642857142857143, 4.970960464763942, 1.51919252567572, 'HP:0011793', 'Neoplasm by anatomical site'),
(179292, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0100899', 'abnormal secondary spermatogonium', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(179293, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0101188', 'abnormal posterior ventral blood island', 0.43333333333333335, 5.574066539846944, 1.5541649957239663, 'HP:0001871', 'Abnormality of blood and blood-forming tissues'),
(179294, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0100894', 'abnormal nucleus', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(179295, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0100691', 'abnormal keratin accumulating cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(179296, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:00000000', 'Xenopus phenotype', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(179297, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0101061', 'abnormal plasma membrane', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(179298, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0101377', 'abnormal manicotto glandulare', 0.4482758620689655, 4.970960464763942, 1.4927697704779535, 'HP:0011793', 'Neoplasm by anatomical site'),
(179299, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0101141', 'abnormal Keller explant', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(179300, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0100573', 'abnormal extraembryonic structure', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(179301, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0115505', 'dead whole organism', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(179302, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0131685', 'abnormal cortical actin cytoskeleton', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(179303, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0101110', 'abnormal cell-free extract', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(179304, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0100172', 'abnormal stem cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(179305, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0101366', 'abnormal morula cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(179306, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0100976', 'abnormal multiciliated cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(179307, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0141315', 'abnormal anatomical region', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(179308, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0100006', 'abnormal anatomical structure', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(179309, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0100638', 'abnormal polar body', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(179310, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0101409', 'abnormal perivitelline space', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(179311, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0100317', 'abnormal respiratory system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(179312, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0100545', 'abnormal male organism', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(179313, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0107261', 'abnormal dorsal-ventral axis', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(179314, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0142054', 'abnormal digestive tract', 0.4642857142857143, 4.970960464763942, 1.51919252567572, 'HP:0011793', 'Neoplasm by anatomical site'),
(179315, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0115391', 'abnormally undifferentiated alimentary system', 0.48148148148148145, 4.970960464763942, 1.5470699431378068, 'HP:0011793', 'Neoplasm by anatomical site'),
(179316, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0100239', 'abnormal acellular anatomical structure', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(179317, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0142057', 'abnormal desmosome', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(179318, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0107270', 'abnormal proximal-distal axis', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(179319, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0100574', 'abnormal gastrula cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(179320, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0101587', 'abnormal hemangioblast', 0.4642857142857143, 5.574066539846944, 1.6087136056268494, 'UPHENO:0004459', 'abnormal hematopoietic system'),
(179321, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0100754', 'abnormal electrically active cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(179322, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0100585', 'abnormal elastica externa', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(179323, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0101467', 'abnormal alkali secreting cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(179324, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0101004', 'abnormal acid secreting cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(179325, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0100523', 'abnormal midgut', 0.4482758620689655, 4.970960464763942, 1.4927697704779535, 'HP:0011793', 'Neoplasm by anatomical site'),
(179326, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0100546', 'abnormal whole organism', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(179327, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0101228', 'abnormal mesenchymal stem cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(179328, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0100423', 'abnormal process', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(179329, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0101264', 'abnormal mitotic spindle', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(179330, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0115509', 'abnormally semi-viable whole organism', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(179331, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0100308', 'abnormal early embryonic cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(179332, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0100108', 'abnormal cell part', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(179333, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0131677', 'abnormal actin filament', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(179334, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0101326', 'abnormal cementoblast', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(179335, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0115512', 'abnormally semi-erect whole organism', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(179336, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0100289', 'abnormal chondroblast', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(179337, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0100791', 'abnormal multiciliated cell precursor', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(179338, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0107312', 'abnormal filopodium', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(179339, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0101297', 'abnormal barrier cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(179340, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0107323', 'abnormal thrombocyte', 0.40625, 5.574066539846944, 1.5048137864243607, 'UPHENO:0004459', 'abnormal hematopoietic system'),
(179341, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0131675', 'abnormal spindle microtubule', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(179342, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0100081', 'abnormal anatomical entity in vitro', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(179343, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0100724', 'abnormal kinetochore', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(179344, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0100156', 'abnormal foregut', 0.4482758620689655, 4.970960464763942, 1.4927697704779535, 'HP:0011793', 'Neoplasm by anatomical site'),
(179345, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0100031', 'abnormal central nervous system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(179346, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0100492', 'abnormal gall bladder primordium', 0.40625, 4.970960464763942, 1.4210744839065794, 'HP:0011793', 'Neoplasm by anatomical site'),
(179347, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0100986', 'abnormal gut epithelium', 0.43333333333333335, 4.970960464763942, 1.4676794159707953, 'HP:0011793', 'Neoplasm by anatomical site'),
(179348, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0101240', 'abnormal ciliated non-epidermal cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(179349, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0100225', 'abnormal endocrine system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(179350, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0100285', 'abnormal progenitor cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(179351, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0101461', 'abnormal sperm entry point', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(179352, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0141499', 'abnormal tadpole', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(179353, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0100599', 'abnormal adult immune system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(179354, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0100344', 'abnormal portion of organism substance', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(179355, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0107284', 'abnormal migrating myoblast', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(179356, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0101169', 'abnormal hepato-pancreatic duct', 0.41935483870967744, 4.970960464763942, 1.4438131194629262, 'HP:0011793', 'Neoplasm by anatomical site'),
(179357, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0100917', 'abnormal stage III oocyte', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(179358, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0100626', 'abnormal primordial germ cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(179359, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0101157', 'abnormal female organism', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(179360, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0100481', 'abnormal anatomical line', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(179361, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0107253', 'abnormal enteric nervous system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(179362, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0100010', 'abnormal multicellular anatomical structure', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(179363, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0101241', 'abnormal nucleate erythrocyte', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(179364, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0100956', 'abnormal centrosome', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(179365, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0100852', 'abnormal interdigital region', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(179366, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0101480', 'abnormal stage V oocyte', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(179367, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0100653', 'abnormal myoblast', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(179368, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0100704', 'abnormal Merkel cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(179369, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0107259', 'abnormal animal-vegetal axis', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(179370, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0100802', 'abnormal exocrine cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(179371, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0101513', 'abnormal basal body', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(179372, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0100437', 'abnormal proepicardium', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(179373, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0101107', 'abnormal erythroid cell', 0.4642857142857143, 5.574066539846944, 1.6087136056268494, 'HP:0001871', 'Abnormality of blood and blood-forming tissues'),
(179374, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0107288', 'abnormal larval alimentary system', 0.48148148148148145, 4.970960464763942, 1.5470699431378068, 'HP:0011793', 'Neoplasm by anatomical site'),
(179375, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0100232', 'abnormal lymphatic system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(179376, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0101498', 'abnormal stage II oocyte', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(179377, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0100515', 'abnormal somatic stem cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(179378, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0100718', 'abnormal ventral pancreatic bud', 0.41935483870967744, 4.970960464763942, 1.4438131194629262, 'HP:0011793', 'Neoplasm by anatomical site'),
(179379, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0100372', 'abnormal hematological system', 0.5416666666666666, 5.574066539846944, 1.737609289344729, 'UPHENO:0004459', 'abnormal hematopoietic system'),
(179380, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0100392', 'abnormal cilium', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(179381, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0100258', 'abnormal organ part', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(179382, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0100377', 'abnormal connective tissue', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(179383, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0100486', 'abnormal oral evagination', 0.4482758620689655, 4.970960464763942, 1.4927697704779535, 'HP:0011793', 'Neoplasm by anatomical site'),
(179384, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0101547', 'abnormal lampbrush chromosome', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(179385, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0107304', 'abnormal hindgut endoderm', 0.40625, 4.970960464763942, 1.4210744839065794, 'HP:0011793', 'Neoplasm by anatomical site'),
(179386, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0100501', 'abnormal urogenital system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(179387, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0100215', 'abnormal first pancreatic bud', 0.40625, 4.970960464763942, 1.4210744839065794, 'HP:0011793', 'Neoplasm by anatomical site'),
(179388, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0101221', 'abnormal larval immune system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(179389, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0101448', 'abnormal myelin accumulating cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(179390, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0100902', 'abnormal spermatocyte', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(179391, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0100337', 'abnormal zygote', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(179392, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0101472', 'abnormal zygote cortex', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(179393, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0107262', 'abnormal left-right axis', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(179394, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0101569', 'abnormal activin-induced ectoderm', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(179395, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0100533', 'abnormal melanoblast', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(179396, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0100202', 'abnormal embryo', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(179397, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0100176', 'abnormal stage VI oocyte', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(179398, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0100025', 'abnormal oocyte', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(179399, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0100888', 'abnormal microtubule', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(179400, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0101198', 'abnormal digestive enzyme secreting cell', 0.40625, 4.970960464763942, 1.4210744839065794, 'HP:0011793', 'Neoplasm by anatomical site'),
(179401, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0100674', 'abnormal secondary oogonium', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(179402, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0100462', 'abnormal anterior foregut', 0.43333333333333335, 4.970960464763942, 1.4676794159707953, 'HP:0011793', 'Neoplasm by anatomical site'),
(179403, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0101484', 'abnormal bone marrow', 0.40625, 5.574066539846944, 1.5048137864243607, 'HP:0001871', 'Abnormality of blood and blood-forming tissues'),
(179404, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0100274', 'abnormal sensory system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(179405, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0100616', 'abnormal ventral blood island', 0.4482758620689655, 5.574066539846944, 1.5807338433081215, 'UPHENO:0004459', 'abnormal hematopoietic system'),
(179406, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0101021', 'abnormal dorsal foregut', 0.43333333333333335, 4.970960464763942, 1.4676794159707953, 'HP:0011793', 'Neoplasm by anatomical site'),
(179407, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0101333', 'abnormal barrier epithelial cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(179408, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0100907', 'abnormal cytoplasm', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(179409, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0100152', 'abnormal alimentary system', 0.5, 4.970960464763942, 1.5765405901472918, 'HP:0011793', 'Neoplasm by anatomical site'),
(179410, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0100026', 'abnormal germ cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(179411, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0101535', 'abnormal absorptive cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(179412, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0100084', 'abnormal anatomical group', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(179413, 'HP:0012149', 'Bilineage myelodysplasia', 'XPO:0100549', 'abnormal mitotic cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(179414, 'HP:0030915', 'Cerebellar edema', 'XPO:0140579', 'abnormally necrotic cerebellum', 0.484375, 9.66901802336956, 2.164123518903122, 'HP:0001317', 'Abnormal cerebellum morphology'),
(179415, 'HP:0030915', 'Cerebellar edema', 'XPO:0131746', 'abnormal neural tube closure', 0.44680851063829785, 5.483278994082134, 1.5652398285119449, 'HP:0002011', 'Morphological central nervous system abnormality'),
(179416, 'HP:0030915', 'Cerebellar edema', 'XPO:0139757', 'abnormally necrotic neural nucleus', 0.42, 5.483278994082134, 1.5175563177406288, 'HP:0002011', 'Morphological central nervous system abnormality'),
(179417, 'HP:0030915', 'Cerebellar edema', 'XPO:0126615', 'abnormally localised medulla oblongata', 0.4090909090909091, 8.435616811180065, 1.857669009815314, 'HP:0011282', 'Abnormal hindbrain morphology'),
(179418, 'HP:0030915', 'Cerebellar edema', 'XPO:0100436', 'abnormal nucleus of the solitary tract', 0.45, 8.435616811180065, 1.9483396944657851, 'HP:0011282', 'Abnormal hindbrain morphology'),
(179419, 'HP:0030915', 'Cerebellar edema', 'XPO:0102148', 'abnormal cerebellum morphology', 0.5254237288135594, 9.66901802336956, 2.2539590732318864, 'HP:0001317', 'Abnormal cerebellum morphology'),
(179420, 'HP:0030915', 'Cerebellar edema', 'XPO:0102792', 'abnormal ventral funiculus morphology', 0.40384615384615385, 5.483278994082134, 1.4880863994491305, 'HP:0002011', 'Morphological central nervous system abnormality'),
(179421, 'HP:0030915', 'Cerebellar edema', 'XPO:0102892', 'abnormal central canal morphology', 0.40384615384615385, 5.483278994082134, 1.4880863994491305, 'HP:0002011', 'Morphological central nervous system abnormality'),
(179422, 'HP:0030915', 'Cerebellar edema', 'XPO:0140468', 'abnormally necrotic central nervous system', 0.42, 5.483278994082134, 1.5175563177406288, 'HP:0002011', 'Morphological central nervous system abnormality'),
(179423, 'HP:0030915', 'Cerebellar edema', 'XPO:0102667', 'abnormal ventrolateral neural tube morphology', 0.40384615384615385, 5.483278994082134, 1.4880863994491305, 'HP:0002011', 'Morphological central nervous system abnormality'),
(179424, 'HP:0030915', 'Cerebellar edema', 'XPO:0141304', 'abnormal pia mater morphology', 0.4067796610169492, 6.005340694266148, 1.562962076284922, 'UPHENO:0081435', 'abnormal anatomical entity morphology in the brain'),
(179425, 'HP:0030915', 'Cerebellar edema', 'XPO:0102068', 'abnormal nucleus of the solitary tract morphology', 0.40298507462686567, 8.435616811180065, 1.8437536902138099, 'HP:0011282', 'Abnormal hindbrain morphology'),
(179426, 'HP:0030915', 'Cerebellar edema', 'XPO:0100575', 'abnormal diencephalon', 0.41379310344827586, 6.005340694266148, 1.5763783058468588, 'UPHENO:0081435', 'abnormal anatomical entity morphology in the brain'),
(179427, 'HP:0030915', 'Cerebellar edema', 'XPO:0140125', 'abnormally necrotic presumptive midbrain-hindbrain boundary', 0.40384615384615385, 5.483278994082134, 1.4880863994491305, 'HP:0002011', 'Morphological central nervous system abnormality'),
(179428, 'HP:0030915', 'Cerebellar edema', 'XPO:0103231', 'abnormal raphe nucleus morphology', 0.421875, 8.435616811180065, 1.8864717973552083, 'HP:0011282', 'Abnormal hindbrain morphology'),
(179429, 'HP:0030915', 'Cerebellar edema', 'XPO:0101807', 'abnormal migrating neuroblast morphology', 0.40425531914893614, 4.7814666189787065, 1.3902997209433732, 'HP:0012639', 'Abnormal nervous system morphology'),
(179430, 'HP:0030915', 'Cerebellar edema', 'XPO:0101134', 'abnormal nucleus reticularis inferior', 0.45, 8.435616811180065, 1.9483396944657851, 'HP:0011282', 'Abnormal hindbrain morphology'),
(179431, 'HP:0030915', 'Cerebellar edema', 'XPO:0101793', 'abnormal hindbrain morphology', 0.46551724137931033, 8.435616811180065, 1.9816470592094544, 'HP:0011282', 'Abnormal hindbrain morphology'),
(179432, 'HP:0030915', 'Cerebellar edema', 'XPO:0101292', 'abnormal solitary tract', 0.43548387096774194, 8.435616811180065, 1.9166572627711127, 'HP:0011282', 'Abnormal hindbrain morphology'),
(179433, 'HP:0030915', 'Cerebellar edema', 'XPO:0141286', 'abnormal neuron projection morphology', 0.40425531914893614, 4.7814666189787065, 1.3902997209433732, 'HP:0012639', 'Abnormal nervous system morphology'),
(179434, 'HP:0030915', 'Cerebellar edema', 'XPO:0103025', 'abnormal dorsolateral neural tube morphology', 0.40384615384615385, 5.483278994082134, 1.4880863994491305, 'HP:0002011', 'Morphological central nervous system abnormality'),
(179435, 'HP:0030915', 'Cerebellar edema', 'XPO:0102490', 'abnormal presumptive midbrain-hindbrain boundary morphology', 0.4375, 5.483278994082134, 1.5488494310006167, 'HP:0002011', 'Morphological central nervous system abnormality'),
(179436, 'HP:0030915', 'Cerebellar edema', 'XPO:0103058', 'abnormal dorsal funiculus morphology', 0.40384615384615385, 5.483278994082134, 1.4880863994491305, 'HP:0002011', 'Morphological central nervous system abnormality'),
(179437, 'HP:0030915', 'Cerebellar edema', 'XPO:0102250', 'abnormal locus coeruleus morphology', 0.4032258064516129, 8.077623523403872, 1.804745483284844, 'UPHENO:0086932', 'abnormal hindbrain morphology'),
(179438, 'HP:0030915', 'Cerebellar edema', 'XPO:0128014', 'decreased size of the neural nucleus', 0.40384615384615385, 5.483278994082134, 1.4880863994491305, 'HP:0002011', 'Morphological central nervous system abnormality'),
(179439, 'HP:0030915', 'Cerebellar edema', 'XPO:0102385', 'abnormal stria terminalis morphology', 0.4067796610169492, 6.005340694266148, 1.562962076284922, 'UPHENO:0081435', 'abnormal anatomical entity morphology in the brain'),
(179440, 'HP:0030915', 'Cerebellar edema', 'XPO:0101265', 'abnormal nucleus reticularis medialis', 0.45, 8.435616811180065, 1.9483396944657851, 'HP:0011282', 'Abnormal hindbrain morphology'),
(179441, 'HP:0030915', 'Cerebellar edema', 'XPO:0101790', 'abnormal neuromere morphology', 0.45652173913043476, 5.483278994082134, 1.5821618319614958, 'HP:0002011', 'Morphological central nervous system abnormality'),
(179442, 'HP:0030915', 'Cerebellar edema', 'XPO:0101802', 'abnormal anterior neural tube morphology', 0.40384615384615385, 5.483278994082134, 1.4880863994491305, 'HP:0002011', 'Morphological central nervous system abnormality'),
(179443, 'HP:0030915', 'Cerebellar edema', 'XPO:0102897', 'abnormal nucleus reticularis medialis morphology', 0.40298507462686567, 8.435616811180065, 1.8437536902138099, 'HP:0011282', 'Abnormal hindbrain morphology'),
(179444, 'HP:0030915', 'Cerebellar edema', 'XPO:0102070', 'abnormal spinal cord morphology', 0.40384615384615385, 5.483278994082134, 1.4880863994491305, 'HP:0002011', 'Morphological central nervous system abnormality'),
(179445, 'HP:0030915', 'Cerebellar edema', 'XPO:0100304', 'abnormal medulla oblongata', 0.47368421052631576, 8.435616811180065, 1.998954349030099, 'HP:0011282', 'Abnormal hindbrain morphology'),
(179446, 'HP:0030915', 'Cerebellar edema', 'XPO:0128686', 'decreased size of the central nervous system', 0.40384615384615385, 5.483278994082134, 1.4880863994491305, 'HP:0002011', 'Morphological central nervous system abnormality'),
(179447, 'HP:0030915', 'Cerebellar edema', 'XPO:0102169', 'abnormal medium cavity morphology', 0.4222222222222222, 4.7814666189787065, 1.4208594094232423, 'HP:0012639', 'Abnormal nervous system morphology'),
(179448, 'HP:0030915', 'Cerebellar edema', 'XPO:0129145', 'decreased size of the cerebellum', 0.4626865671641791, 9.66901802336956, 2.115118142582451, 'HP:0001317', 'Abnormal cerebellum morphology'),
(179449, 'HP:0030915', 'Cerebellar edema', 'XPO:0102219', 'abnormal vestibuloauditory system morphology', 0.4222222222222222, 4.7814666189787065, 1.4208594094232423, 'HP:0012639', 'Abnormal nervous system morphology'),
(179450, 'HP:0030915', 'Cerebellar edema', 'XPO:0102555', 'abnormal granule cell layer of the cerebellum morphology', 0.5081967213114754, 9.66901802336956, 2.2167009851980426, 'HP:0001317', 'Abnormal cerebellum morphology'),
(179451, 'HP:0030915', 'Cerebellar edema', 'XPO:0142031', 'abnormally necrotic cerebrospinal fluid', 0.45652173913043476, 5.483278994082134, 1.5821618319614958, 'HP:0002011', 'Morphological central nervous system abnormality'),
(179452, 'HP:0030915', 'Cerebellar edema', 'XPO:0100157', 'abnormal optic tract', 0.4067796610169492, 6.005340694266148, 1.562962076284922, 'UPHENO:0081435', 'abnormal anatomical entity morphology in the brain'),
(179453, 'HP:0030915', 'Cerebellar edema', 'XPO:0103181', 'abnormal dorsal column nucleus morphology', 0.40298507462686567, 8.435616811180065, 1.8437536902138099, 'HP:0011282', 'Abnormal hindbrain morphology'),
(179454, 'HP:0030915', 'Cerebellar edema', 'XPO:0100729', 'abnormal thalamus', 0.4067796610169492, 6.005340694266148, 1.562962076284922, 'UPHENO:0081435', 'abnormal anatomical entity morphology in the brain'),
(179455, 'HP:0030915', 'Cerebellar edema', 'XPO:0130621', 'increased size of the cerebellum', 0.45588235294117646, 9.66901802336956, 2.099508201251988, 'HP:0001317', 'Abnormal cerebellum morphology'),
(179456, 'HP:0030915', 'Cerebellar edema', 'XPO:0101936', 'abnormal medulla oblongata morphology', 0.421875, 8.435616811180065, 1.8864717973552083, 'HP:0011282', 'Abnormal hindbrain morphology'),
(179457, 'HP:0030915', 'Cerebellar edema', 'XPO:0101796', 'abnormal neural nucleus morphology', 0.4666666666666667, 5.483278994082134, 1.5996448138795258, 'HP:0002011', 'Morphological central nervous system abnormality'),
(179458, 'HP:0030915', 'Cerebellar edema', 'XPO:0103133', 'abnormal parabrachial area morphology', 0.44680851063829785, 5.483278994082134, 1.5652398285119449, 'HP:0002011', 'Morphological central nervous system abnormality'),
(179459, 'HP:0030915', 'Cerebellar edema', 'XPO:0126702', 'abnormally localised raphe nucleus', 0.4090909090909091, 8.435616811180065, 1.857669009815314, 'HP:0011282', 'Abnormal hindbrain morphology'),
(179460, 'HP:0030915', 'Cerebellar edema', 'XPO:0140608', 'abnormally necrotic ventricular zone', 0.4067796610169492, 6.005340694266148, 1.562962076284922, 'UPHENO:0081435', 'abnormal anatomical entity morphology in the brain'),
(179461, 'HP:0030915', 'Cerebellar edema', 'XPO:0103144', 'abnormal lateral funiculus morphology', 0.40384615384615385, 5.483278994082134, 1.4880863994491305, 'HP:0002011', 'Morphological central nervous system abnormality'),
(179462, 'HP:0030915', 'Cerebellar edema', 'XPO:0101549', 'abnormal dorsal column nucleus', 0.45, 8.435616811180065, 1.9483396944657851, 'HP:0011282', 'Abnormal hindbrain morphology'),
(179463, 'HP:0030915', 'Cerebellar edema', 'XPO:0101862', 'abnormal brain ventricle morphology', 0.42105263157894735, 6.005340694266148, 1.590146063369307, 'UPHENO:0081435', 'abnormal anatomical entity morphology in the brain'),
(179464, 'HP:0030915', 'Cerebellar edema', 'XPO:0101354', 'abnormal eminentia thalami', 0.4067796610169492, 6.005340694266148, 1.562962076284922, 'UPHENO:0081435', 'abnormal anatomical entity morphology in the brain'),
(179465, 'HP:0030915', 'Cerebellar edema', 'XPO:0140715', 'abnormally necrotic granule cell layer of the cerebellum', 0.4696969696969697, 9.66901802336956, 2.1310815248418034, 'HP:0001317', 'Abnormal cerebellum morphology'),
(179466, 'HP:0030915', 'Cerebellar edema', 'XPO:0142037', 'decreased size of the cerebrospinal fluid', 0.4375, 5.483278994082134, 1.5488494310006167, 'HP:0002011', 'Morphological central nervous system abnormality'),
(179467, 'HP:0030915', 'Cerebellar edema', 'XPO:0102392', 'abnormal Stirnorgan morphology', 0.40425531914893614, 4.7814666189787065, 1.3902997209433732, 'HP:0012639', 'Abnormal nervous system morphology'),
(179468, 'HP:0030915', 'Cerebellar edema', 'XPO:0100541', 'abnormal nucleus reticularis superior', 0.45, 8.435616811180065, 1.9483396944657851, 'HP:0011282', 'Abnormal hindbrain morphology'),
(179469, 'HP:0030915', 'Cerebellar edema', 'XPO:0130251', 'increased size of the granule cell layer of the cerebellum', 0.45588235294117646, 9.66901802336956, 2.099508201251988, 'HP:0001317', 'Abnormal cerebellum morphology'),
(179470, 'HP:0030915', 'Cerebellar edema', 'XPO:0102235', 'abnormal lateral ventricle morphology', 0.4067796610169492, 6.005340694266148, 1.562962076284922, 'UPHENO:0081435', 'abnormal anatomical entity morphology in the brain'),
(179471, 'HP:0030915', 'Cerebellar edema', 'XPO:0101828', 'abnormal neuron morphology', 0.40425531914893614, 4.7814666189787065, 1.3902997209433732, 'HP:0012639', 'Abnormal nervous system morphology'),
(179472, 'HP:0030915', 'Cerebellar edema', 'XPO:0101186', 'abnormal optic chiasm', 0.4067796610169492, 6.005340694266148, 1.562962076284922, 'UPHENO:0081435', 'abnormal anatomical entity morphology in the brain'),
(179473, 'HP:0030915', 'Cerebellar edema', 'XPO:0142044', 'increased size of the cerebrospinal fluid', 0.4375, 5.483278994082134, 1.5488494310006167, 'HP:0002011', 'Morphological central nervous system abnormality'),
(179474, 'HP:0030915', 'Cerebellar edema', 'XPO:0102334', 'abnormal glial cell morphology', 0.40425531914893614, 4.7814666189787065, 1.3902997209433732, 'HP:0012639', 'Abnormal nervous system morphology'),
(179475, 'HP:0030915', 'Cerebellar edema', 'XPO:0100763', 'abnormal pretectum', 0.4067796610169492, 6.005340694266148, 1.562962076284922, 'UPHENO:0081435', 'abnormal anatomical entity morphology in the brain'),
(179476, 'HP:0030915', 'Cerebellar edema', 'XPO:0102766', 'abnormal nucleus reticularis inferior morphology', 0.40298507462686567, 8.435616811180065, 1.8437536902138099, 'HP:0011282', 'Abnormal hindbrain morphology'),
(179477, 'HP:0030915', 'Cerebellar edema', 'XPO:0139854', 'abnormally necrotic hindbrain', 0.42857142857142855, 8.435616811180065, 1.9013848499576826, 'HP:0011282', 'Abnormal hindbrain morphology'),
(179478, 'HP:0030915', 'Cerebellar edema', 'XPO:0101906', 'abnormal sensory system morphology', 0.4418604651162791, 4.7814666189787065, 1.4535271116150168, 'HP:0012639', 'Abnormal nervous system morphology'),
(179479, 'HP:0030915', 'Cerebellar edema', 'XPO:0140221', 'abnormally necrotic nervous system', 0.40425531914893614, 4.7814666189787065, 1.3902997209433732, 'HP:0012639', 'Abnormal nervous system morphology'),
(179480, 'HP:0030915', 'Cerebellar edema', 'XPO:0103729', 'increased size of the hindbrain', 0.40298507462686567, 8.435616811180065, 1.8437536902138099, 'HP:0011282', 'Abnormal hindbrain morphology'),
(179481, 'HP:0030915', 'Cerebellar edema', 'XPO:0101599', 'abnormal raphe nucleus', 0.46551724137931033, 8.435616811180065, 1.9816470592094544, 'HP:0011282', 'Abnormal hindbrain morphology'),
(179482, 'HP:0030915', 'Cerebellar edema', 'XPO:0102633', 'abnormal ventricular zone morphology', 0.42857142857142855, 6.005340694266148, 1.6042809730218013, 'UPHENO:0081435', 'abnormal anatomical entity morphology in the brain'),
(179483, 'HP:0030915', 'Cerebellar edema', 'XPO:0102059', 'abnormal olfactory system morphology', 0.41304347826086957, 4.7814666189787065, 1.405330425021534, 'HP:0012639', 'Abnormal nervous system morphology'),
(179484, 'HP:0030915', 'Cerebellar edema', 'XPO:0107340', 'abnormal enteric nervous system morphology', 0.4318181818181818, 4.7814666189787065, 1.4369148276191301, 'HP:0012639', 'Abnormal nervous system morphology'),
(179485, 'HP:0030915', 'Cerebellar edema', 'XPO:0101905', 'abnormal visual system morphology', 0.4222222222222222, 4.7814666189787065, 1.4208594094232423, 'HP:0012639', 'Abnormal nervous system morphology'),
(179486, 'HP:0030915', 'Cerebellar edema', 'XPO:0139852', 'abnormally necrotic neuromere', 0.4117647058823529, 5.483278994082134, 1.502604659339613, 'HP:0002011', 'Morphological central nervous system abnormality'),
(179487, 'HP:0030915', 'Cerebellar edema', 'XPO:0102274', 'abnormal gustatory system morphology', 0.41304347826086957, 4.7814666189787065, 1.405330425021534, 'HP:0012639', 'Abnormal nervous system morphology'),
(179488, 'HP:0030915', 'Cerebellar edema', 'XPO:0102548', 'abnormal principal cavity morphology', 0.4222222222222222, 4.7814666189787065, 1.4208594094232423, 'HP:0012639', 'Abnormal nervous system morphology'),
(179489, 'HP:0030915', 'Cerebellar edema', 'XPO:0103344', 'decreased size of the hindbrain', 0.40298507462686567, 8.435616811180065, 1.8437536902138099, 'HP:0011282', 'Abnormal hindbrain morphology'),
(179490, 'HP:0030915', 'Cerebellar edema', 'XPO:0130165', 'increased size of the central nervous system', 0.40384615384615385, 5.483278994082134, 1.4880863994491305, 'HP:0002011', 'Morphological central nervous system abnormality'),
(179491, 'HP:0030915', 'Cerebellar edema', 'XPO:0129494', 'increased size of the neural nucleus', 0.40384615384615385, 5.483278994082134, 1.4880863994491305, 'HP:0002011', 'Morphological central nervous system abnormality'),
(179492, 'HP:0030915', 'Cerebellar edema', 'XPO:0101664', 'abnormal nervous system morphology', 0.4523809523809524, 4.7814666189787065, 1.4707292146657451, 'HP:0012639', 'Abnormal nervous system morphology'),
(179493, 'HP:0030915', 'Cerebellar edema', 'XPO:0100590', 'abnormal hypothalamus', 0.4067796610169492, 6.005340694266148, 1.562962076284922, 'UPHENO:0081435', 'abnormal anatomical entity morphology in the brain'),
(179494, 'HP:0030915', 'Cerebellar edema', 'XPO:0102419', 'abnormal posterior neural tube morphology', 0.40384615384615385, 5.483278994082134, 1.4880863994491305, 'HP:0002011', 'Morphological central nervous system abnormality'),
(179495, 'HP:0030915', 'Cerebellar edema', 'XPO:0128773', 'decreased size of the granule cell layer of the cerebellum', 0.45588235294117646, 9.66901802336956, 2.099508201251988, 'HP:0001317', 'Abnormal cerebellum morphology'),
(179496, 'HP:0030915', 'Cerebellar edema', 'XPO:0142058', 'abnormal cerebrospinal fluid morphology', 0.4883720930232558, 5.483278994082134, 1.6364230623437035, 'HP:0002011', 'Morphological central nervous system abnormality'),
(179497, 'HP:0030915', 'Cerebellar edema', 'XPO:0102173', 'abnormal nucleus reticularis superior morphology', 0.40298507462686567, 8.435616811180065, 1.8437536902138099, 'HP:0011282', 'Abnormal hindbrain morphology'),
(179498, 'HP:0030915', 'Cerebellar edema', 'XPO:0101663', 'abnormal central nervous system morphology', 0.4772727272727273, 5.483278994082134, 1.617720470261422, 'HP:0002011', 'Morphological central nervous system abnormality'),
(179499, 'HP:0031457', 'Pulmonary opacity', 'XPO:0126855', 'abnormally localised pharynx', 0.4528301886792453, 7.241224942262181, 1.810813424092455, 'HP:0012252', 'Abnormal respiratory system morphology'),
(179500, 'HP:0031457', 'Pulmonary opacity', 'XPO:0102356', 'abnormal kinetochore morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(179501, 'HP:0031457', 'Pulmonary opacity', 'XPO:0141277', 'abnormal actin cytoskeleton morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(179502, 'HP:0031457', 'Pulmonary opacity', 'XPO:0102668', 'abnormal pharynx morphology', 0.4528301886792453, 7.241224942262181, 1.810813424092455, 'HP:0012252', 'Abnormal respiratory system morphology'),
(179503, 'HP:0031457', 'Pulmonary opacity', 'XPO:0102526', 'abnormal nucleus morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(179504, 'HP:0031457', 'Pulmonary opacity', 'XPO:0101716', 'abnormal anatomical group morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(179505, 'HP:0031457', 'Pulmonary opacity', 'XPO:0139718', 'abnormally necrotic anatomical structure', 0.41935483870967744, 2.786899518863159, 1.0810641970914296, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(179506, 'HP:0031457', 'Pulmonary opacity', 'XPO:0141648', 'neoplastic lung', 0.41379310344827586, 7.241224942262181, 1.7310022939400542, 'HP:0012252', 'Abnormal respiratory system morphology'),
(179507, 'HP:0031457', 'Pulmonary opacity', 'XPO:0127859', 'abnormally localised larynx', 0.47058823529411764, 7.241224942262181, 1.8459781328463531, 'HP:0012252', 'Abnormal respiratory system morphology'),
(179508, 'HP:0031457', 'Pulmonary opacity', 'XPO:0101694', 'abnormal anatomical space morphology', 0.41935483870967744, 2.786899518863159, 1.0810641970914296, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(179509, 'HP:0031457', 'Pulmonary opacity', 'XPO:0126197', 'absent larynx', 0.46153846153846156, 7.241224942262181, 1.8281421770490451, 'HP:0012252', 'Abnormal respiratory system morphology'),
(179510, 'HP:0031457', 'Pulmonary opacity', 'XPO:0102520', 'abnormal microtubule morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(179511, 'HP:0031457', 'Pulmonary opacity', 'XPO:0103201', 'abnormal activin-induced ectoderm morphology', 0.41935483870967744, 2.786899518863159, 1.0810641970914296, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(179512, 'HP:0031457', 'Pulmonary opacity', 'XPO:0102055', 'abnormal process morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(179513, 'HP:0031457', 'Pulmonary opacity', 'XPO:0130015', 'increased size of the respiratory system', 0.5581395348837209, 7.241224942262181, 2.0103765620556295, 'HP:0012252', 'Abnormal respiratory system morphology'),
(179514, 'HP:0031457', 'Pulmonary opacity', 'XPO:0100117', 'abnormal aortic arch', 0.42857142857142855, 7.241224942262181, 1.7616418813460253, 'HP:0012252', 'Abnormal respiratory system morphology'),
(179515, 'HP:0031457', 'Pulmonary opacity', 'XPO:0102436', 'abnormal larynx morphology', 0.4897959183673469, 7.241224942262181, 1.8832743880539138, 'HP:0012252', 'Abnormal respiratory system morphology'),
(179516, 'HP:0031457', 'Pulmonary opacity', 'XPO:0100586', 'abnormal thyroid primordium', 0.4897959183673469, 7.241224942262181, 1.8832743880539138, 'HP:0012252', 'Abnormal respiratory system morphology'),
(179517, 'HP:0031457', 'Pulmonary opacity', 'XPO:0103145', 'abnormal basal body morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(179518, 'HP:0031457', 'Pulmonary opacity', 'XPO:0102360', 'abnormal cell condensation morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(179519, 'HP:0031457', 'Pulmonary opacity', 'XPO:0101548', 'abnormal pulmonary vein', 0.4444444444444444, 7.241224942262181, 1.793968281927239, 'HP:0012252', 'Abnormal respiratory system morphology'),
(179520, 'HP:0031457', 'Pulmonary opacity', 'XPO:0100210', 'abnormal pulmonary artery', 0.4444444444444444, 7.241224942262181, 1.793968281927239, 'HP:0012252', 'Abnormal respiratory system morphology'),
(179521, 'HP:0031457', 'Pulmonary opacity', 'XPO:0102528', 'abnormal bronchus morphology', 0.42105263157894735, 7.241224942262181, 1.746120504946495, 'HP:0012252', 'Abnormal respiratory system morphology'),
(179522, 'HP:0031457', 'Pulmonary opacity', 'XPO:0102703', 'abnormal endoplasmic reticulum morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(179523, 'HP:0031457', 'Pulmonary opacity', 'XPO:0115510', 'abnormal degeneration of whole organism', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(179524, 'HP:0031457', 'Pulmonary opacity', 'XPO:0101036', 'abnormal pharynx', 0.5333333333333333, 7.241224942262181, 1.9651937909206725, 'HP:0012252', 'Abnormal respiratory system morphology'),
(179525, 'HP:0031457', 'Pulmonary opacity', 'XPO:0102742', 'abnormal cell-free extract morphology', 0.41935483870967744, 2.786899518863159, 1.0810641970914296, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(179526, 'HP:0031457', 'Pulmonary opacity', 'XPO:0100716', 'abnormal aortic arch 3', 0.42105263157894735, 7.241224942262181, 1.746120504946495, 'HP:0012252', 'Abnormal respiratory system morphology'),
(179527, 'HP:0031457', 'Pulmonary opacity', 'XPO:0141614', 'metaplastic larynx', 0.5454545454545454, 7.241224942262181, 1.987400075328502, 'HP:0012252', 'Abnormal respiratory system morphology'),
(179528, 'HP:0031457', 'Pulmonary opacity', 'XPO:0101871', 'abnormal acellular anatomical structure morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(179529, 'HP:0031457', 'Pulmonary opacity', 'XPO:0101740', 'abnormal cell part morphology', 0.42857142857142855, 2.786899518863159, 1.092879457252359, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(179530, 'HP:0031457', 'Pulmonary opacity', 'XPO:0101638', 'abnormal anatomical structure morphology', 0.4482758620689655, 2.786899518863159, 1.1177207989108764, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(179531, 'HP:0031457', 'Pulmonary opacity', 'XPO:0101329', 'abnormal pharyngeal epithelium', 0.5217391304347826, 7.241224942262181, 1.9437156182576012, 'HP:0012252', 'Abnormal respiratory system morphology'),
(179532, 'HP:0031457', 'Pulmonary opacity', 'XPO:0102974', 'abnormal trachea morphology', 0.41379310344827586, 7.241224942262181, 1.7310022939400542, 'HP:0012252', 'Abnormal respiratory system morphology'),
(179533, 'HP:0031457', 'Pulmonary opacity', 'XPO:0102588', 'abnormal centrosome morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(179534, 'HP:0031457', 'Pulmonary opacity', 'XPO:0101949', 'abnormal respiratory system morphology', 0.6666666666666666, 7.241224942262181, 2.197153452729566, 'HP:0012252', 'Abnormal respiratory system morphology'),
(179535, 'HP:0031457', 'Pulmonary opacity', 'XPO:0140110', 'abnormally necrotic pharynx', 0.41379310344827586, 7.241224942262181, 1.7310022939400542, 'HP:0012252', 'Abnormal respiratory system morphology'),
(179536, 'HP:0031457', 'Pulmonary opacity', 'XPO:0100317', 'abnormal respiratory system', 0.40625, 6.780552239366747, 1.6596985711998251, 'UPHENO:0004536', 'abnormal respiratory system'),
(179537, 'HP:0031457', 'Pulmonary opacity', 'XPO:0100804', 'abnormal larynx', 0.5853658536585366, 7.241224942262181, 2.058826320955896, 'HP:0012252', 'Abnormal respiratory system morphology'),
(179538, 'HP:0031457', 'Pulmonary opacity', 'XPO:0141316', 'abnormal anatomical region morphology', 0.41935483870967744, 2.786899518863159, 1.0810641970914296, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(179539, 'HP:0031457', 'Pulmonary opacity', 'XPO:0100116', 'abnormal aortic arch 1', 0.42105263157894735, 7.241224942262181, 1.746120504946495, 'HP:0012252', 'Abnormal respiratory system morphology'),
(179540, 'HP:0031457', 'Pulmonary opacity', 'XPO:0102353', 'abnormal centromere morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(179541, 'HP:0031457', 'Pulmonary opacity', 'XPO:0130620', 'increased size of the larynx', 0.41379310344827586, 7.241224942262181, 1.7310022939400542, 'HP:0012252', 'Abnormal respiratory system morphology'),
(179542, 'HP:0031457', 'Pulmonary opacity', 'XPO:0125599', 'absent pharyngeal epithelium', 0.41379310344827586, 7.241224942262181, 1.7310022939400542, 'HP:0012252', 'Abnormal respiratory system morphology'),
(179543, 'HP:0031457', 'Pulmonary opacity', 'XPO:0141178', 'abnormally necrotic larynx', 0.42857142857142855, 7.241224942262181, 1.7616418813460253, 'HP:0012252', 'Abnormal respiratory system morphology'),
(179544, 'HP:0031457', 'Pulmonary opacity', 'XPO:0100360', 'abnormal aortic arch 6', 0.42105263157894735, 7.241224942262181, 1.746120504946495, 'HP:0012252', 'Abnormal respiratory system morphology'),
(179545, 'HP:0031457', 'Pulmonary opacity', 'XPO:0102113', 'abnormal anatomical line morphology', 0.4482758620689655, 2.786899518863159, 1.1177207989108764, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(179546, 'HP:0031457', 'Pulmonary opacity', 'XPO:0101713', 'abnormal anatomical entity in vitro morphology', 0.4482758620689655, 2.786899518863159, 1.1177207989108764, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(179547, 'HP:0031457', 'Pulmonary opacity', 'XPO:0101976', 'abnormal portion of organism substance morphology', 0.4482758620689655, 2.786899518863159, 1.1177207989108764, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(179548, 'HP:0031457', 'Pulmonary opacity', 'XPO:0102539', 'abnormal cytoplasm morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(179549, 'HP:0031457', 'Pulmonary opacity', 'XPO:0139850', 'abnormally necrotic respiratory system', 0.5853658536585366, 7.241224942262181, 2.058826320955896, 'HP:0012252', 'Abnormal respiratory system morphology'),
(179550, 'HP:0031457', 'Pulmonary opacity', 'XPO:0140269', 'abnormally necrotic anatomical line', 0.41935483870967744, 2.786899518863159, 1.0810641970914296, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(179551, 'HP:0031457', 'Pulmonary opacity', 'XPO:0101642', 'abnormal multicellular anatomical structure morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(179552, 'HP:0031457', 'Pulmonary opacity', 'XPO:0142064', 'abnormal desmosome morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(179553, 'HP:0031457', 'Pulmonary opacity', 'XPO:0101636', 'abnormal cell morphology', 0.4166666666666667, 2.786899518863159, 1.0775936770692605, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(179554, 'HP:0031457', 'Pulmonary opacity', 'XPO:0101890', 'abnormal organ part morphology', 0.41935483870967744, 2.786899518863159, 1.0810641970914296, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(179555, 'HP:0031457', 'Pulmonary opacity', 'XPO:0102896', 'abnormal mitotic spindle morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(179556, 'HP:0031457', 'Pulmonary opacity', 'XPO:0107399', 'abnormal filopodium morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(179557, 'HP:0031457', 'Pulmonary opacity', 'XPO:0141593', 'edematous lung', 0.41379310344827586, 7.241224942262181, 1.7310022939400542, 'HP:0012252', 'Abnormal respiratory system morphology'),
(179558, 'HP:0031457', 'Pulmonary opacity', 'XPO:0127240', 'abnormally localised pharyngeal epithelium', 0.41379310344827586, 7.241224942262181, 1.7310022939400542, 'HP:0012252', 'Abnormal respiratory system morphology'),
(179559, 'HP:0031457', 'Pulmonary opacity', 'XPO:0102178', 'abnormal whole organism morphology', 0.41935483870967744, 2.786899518863159, 1.0810641970914296, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(179560, 'HP:0031457', 'Pulmonary opacity', 'XPO:0101474', 'abnormal aortic arch 5', 0.42105263157894735, 7.241224942262181, 1.746120504946495, 'HP:0012252', 'Abnormal respiratory system morphology'),
(179561, 'HP:0031457', 'Pulmonary opacity', 'XPO:0101210', 'abnormal aortic arch 2', 0.42105263157894735, 7.241224942262181, 1.746120504946495, 'HP:0012252', 'Abnormal respiratory system morphology'),
(179562, 'HP:0031457', 'Pulmonary opacity', 'XPO:0102932', 'abnormal lung morphology', 0.43636363636363634, 7.241224942262181, 1.777584666769093, 'HP:0012252', 'Abnormal respiratory system morphology'),
(179563, 'HP:0031457', 'Pulmonary opacity', 'XPO:0100875', 'abnormal oropharynx', 0.5, 7.241224942262181, 1.9027907060764961, 'HP:0012252', 'Abnormal respiratory system morphology'),
(179564, 'HP:0031457', 'Pulmonary opacity', 'XPO:0103175', 'abnormal external gill morphology', 0.43902439024390244, 7.034007514759976, 1.7572993086376965, 'UPHENO:0087433', 'abnormal respiratory system morphology'),
(179565, 'HP:0031457', 'Pulmonary opacity', 'XPO:0100262', 'abnormal aortic arch 4', 0.42105263157894735, 7.241224942262181, 1.746120504946495, 'HP:0012252', 'Abnormal respiratory system morphology'),
(179566, 'HP:0031457', 'Pulmonary opacity', 'XPO:0102693', 'abnormal plasma membrane morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(179567, 'HP:0031457', 'Pulmonary opacity', 'XPO:0126955', 'abnormally localised oropharynx', 0.42857142857142855, 7.241224942262181, 1.7616418813460253, 'HP:0012252', 'Abnormal respiratory system morphology'),
(179568, 'HP:0031457', 'Pulmonary opacity', 'XPO:0129144', 'decreased size of the larynx', 0.41379310344827586, 7.241224942262181, 1.7310022939400542, 'HP:0012252', 'Abnormal respiratory system morphology'),
(179569, 'HP:0031457', 'Pulmonary opacity', 'XPO:0141296', 'abnormal adherens junction morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(179570, 'HP:0031457', 'Pulmonary opacity', 'XPO:0140144', 'abnormally necrotic portion of organism substance', 0.41935483870967744, 2.786899518863159, 1.0810641970914296, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(179571, 'HP:0031457', 'Pulmonary opacity', 'XPO:0125232', 'absent pharynx', 0.4444444444444444, 7.241224942262181, 1.793968281927239, 'HP:0012252', 'Abnormal respiratory system morphology'),
(179572, 'HP:0031457', 'Pulmonary opacity', 'XPO:0128535', 'decreased size of the respiratory system', 0.5581395348837209, 7.241224942262181, 2.0103765620556295, 'HP:0012252', 'Abnormal respiratory system morphology'),
(179573, 'HP:0031457', 'Pulmonary opacity', 'XPO:0102773', 'abnormal Keller explant morphology', 0.41935483870967744, 2.786899518863159, 1.0810641970914296, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(179574, 'HP:0031457', 'Pulmonary opacity', 'XPO:0107345', 'abnormal anatomical axis morphology', 0.41935483870967744, 2.786899518863159, 1.0810641970914296, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(179575, 'HP:0031457', 'Pulmonary opacity', 'XPO:0102601', 'abnormal disaggregated/reaggregated ectoderm treated with activin morphology', 0.41935483870967744, 2.786899518863159, 1.0810641970914296, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(179576, 'HP:0031457', 'Pulmonary opacity', 'XPO:0102961', 'abnormal pharyngeal epithelium morphology', 0.4067796610169492, 7.241224942262181, 1.7162700916117157, 'HP:0012252', 'Abnormal respiratory system morphology'),
(179577, 'HP:0031457', 'Pulmonary opacity', 'XPO:0103179', 'abnormal lampbrush chromosome morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(179578, 'HP:0031457', 'Pulmonary opacity', 'XPO:0141644', 'neoplastic larynx', 0.46153846153846156, 7.241224942262181, 1.8281421770490451, 'HP:0012252', 'Abnormal respiratory system morphology'),
(179579, 'HP:0031457', 'Pulmonary opacity', 'XPO:0125326', 'absent oropharynx', 0.41379310344827586, 7.241224942262181, 1.7310022939400542, 'HP:0012252', 'Abnormal respiratory system morphology'),
(179580, 'HP:0032021', 'Eosinophilic liver infiltration', 'XPO:0100042', 'abnormal hepatic vein', 0.5147058823529411, 10.01729298920255, 2.2706738265976094, 'UPHENO:0019492', 'abnormal liver morphology'),
(179581, 'HP:0032021', 'Eosinophilic liver infiltration', 'XPO:0103168', 'abnormal liver parenchyme morphology', 0.5588235294117647, 14.404694921567193, 2.83719623152328, 'UPHENO:0019417', 'abnormal liver parenchyma morphology'),
(179582, 'HP:0032021', 'Eosinophilic liver infiltration', 'XPO:0141125', 'abnormally necrotic liver parenchyme', 0.5205479452054794, 14.404694921567193, 2.7383086646201167, 'UPHENO:0019417', 'abnormal liver parenchyma morphology'),
(179583, 'HP:0032021', 'Eosinophilic liver infiltration', 'XPO:0101674', 'abnormal hepatic vein morphology', 0.4117647058823529, 10.01729298920255, 2.0309524124007297, 'UPHENO:0019492', 'abnormal liver morphology'),
(179584, 'HP:0032021', 'Eosinophilic liver infiltration', 'XPO:0127068', 'abnormally localised hepatic vein', 0.44871794871794873, 10.01729298920255, 2.1201271569935747, 'UPHENO:0019492', 'abnormal liver morphology'),
(179585, 'HP:0032021', 'Eosinophilic liver infiltration', 'XPO:0102426', 'abnormal liver morphology', 0.49295774647887325, 10.01729298920255, 2.2221841007837098, 'UPHENO:0019492', 'abnormal liver morphology'),
(179586, 'HP:0032021', 'Eosinophilic liver infiltration', 'XPO:0102825', 'abnormal bile duct morphology', 0.4090909090909091, 8.69832224767236, 1.8863733871813304, 'UPHENO:0087100', 'abnormal hepatobiliary system morphology'),
(179587, 'HP:0032021', 'Eosinophilic liver infiltration', 'XPO:0139877', 'abnormally necrotic liver', 0.4268292682926829, 10.01729298920255, 2.067770257271041, 'UPHENO:0019492', 'abnormal liver morphology'),
(179588, 'HP:0032021', 'Eosinophilic liver infiltration', 'XPO:0101787', 'abnormal hepatic portal vein morphology', 0.4117647058823529, 10.01729298920255, 2.0309524124007297, 'UPHENO:0019492', 'abnormal liver morphology'),
(179589, 'HP:0032021', 'Eosinophilic liver infiltration', 'XPO:0129248', 'decreased size of the liver parenchyme', 0.5066666666666667, 14.404694921567193, 2.7015511766873326, 'UPHENO:0019417', 'abnormal liver parenchyma morphology'),
(179590, 'HP:0032021', 'Eosinophilic liver infiltration', 'XPO:0140908', 'abnormally necrotic hepatocyte', 0.4125, 9.184143847054914, 1.9463965004361654, 'UPHENO:0086622', 'abnormal liver morphology'),
(179591, 'HP:0032021', 'Eosinophilic liver infiltration', 'XPO:0125433', 'absent hepatic vein', 0.43209876543209874, 10.01729298920255, 2.0804951174194186, 'UPHENO:0019492', 'abnormal liver morphology'),
(179592, 'HP:0032021', 'Eosinophilic liver infiltration', 'XPO:0102211', 'abnormal biliary tree morphology', 0.4153846153846154, 8.69832224767236, 1.900828567057226, 'UPHENO:0087100', 'abnormal hepatobiliary system morphology'),
(179593, 'HP:0032021', 'Eosinophilic liver infiltration', 'XPO:0130724', 'increased size of the liver parenchyme', 0.5066666666666667, 14.404694921567193, 2.7015511766873326, 'UPHENO:0019417', 'abnormal liver parenchyma morphology'),
(179594, 'HP:0032021', 'Eosinophilic liver infiltration', 'XPO:0141647', 'neoplastic liver', 0.47297297297297297, 10.01729298920255, 2.176673803362472, 'UPHENO:0019492', 'abnormal liver morphology'),
(179595, 'HP:0032021', 'Eosinophilic liver infiltration', 'XPO:0102763', 'abnormal hepatocyte morphology', 0.44, 9.184143847054914, 2.010229661681511, 'UPHENO:0086622', 'abnormal liver morphology'),
(179596, 'HP:0032021', 'Eosinophilic liver infiltration', 'XPO:0128672', 'decreased size of the liver', 0.4117647058823529, 10.01729298920255, 2.0309524124007297, 'UPHENO:0019492', 'abnormal liver morphology'),
(179597, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0100907', 'abnormal cytoplasm', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(179598, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0141745', 'abnormal creatinine homeostasis', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(179599, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0100423', 'abnormal process', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(179600, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0101480', 'abnormal stage V oocyte', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(179601, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0101467', 'abnormal alkali secreting cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(179602, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0101535', 'abnormal absorptive cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(179603, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0100724', 'abnormal kinetochore', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(179604, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0100581', 'abnormal immune system', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(179605, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0101241', 'abnormal nucleate erythrocyte', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(179606, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0101326', 'abnormal cementoblast', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(179607, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0141772', 'abnormal water homeostasis', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(179608, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0100721', 'abnormal centromere', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(179609, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0141797', 'abnormal hydrogen metabolic process', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(179610, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0141778', 'abnormal biosynthetic process', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(179611, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0100477', 'abnormal pericyte', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(179612, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0100307', 'abnormal blastomere', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(179613, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0141738', 'abnormal carbon dioxide homeostasis', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(179614, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0131667', 'abnormal actin cytoskeleton', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(179615, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0100902', 'abnormal spermatocyte', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(179616, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0100754', 'abnormal electrically active cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(179617, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0107253', 'abnormal enteric nervous system', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(179618, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0100574', 'abnormal gastrula cell', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(179619, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0101240', 'abnormal ciliated non-epidermal cell', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(179620, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0141315', 'abnormal anatomical region', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(179621, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0101472', 'abnormal zygote cortex', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(179622, 'HP:0033771', 'Pleuritic chest pain', 'XPO:00000000', 'Xenopus phenotype', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(179623, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0107260', 'abnormal anterior-posterior axis', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(179624, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0101569', 'abnormal activin-induced ectoderm', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(179625, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0100285', 'abnormal progenitor cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(179626, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0100386', 'abnormal limb', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(179627, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0133403', 'abnormal developmental process', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(179628, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0100791', 'abnormal multiciliated cell precursor', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(179629, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0100802', 'abnormal exocrine cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(179630, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0142057', 'abnormal desmosome', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(179631, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0131723', 'abnormal pathway-restricted SMAD protein phosphorylation', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(179632, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0100533', 'abnormal melanoblast', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(179633, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0101498', 'abnormal stage II oocyte', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(179634, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0141782', 'abnormal methylation', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(179635, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0100715', 'abnormal ciliated cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(179636, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0100704', 'abnormal Merkel cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(179637, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0100108', 'abnormal cell part', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(179638, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0141783', 'abnormal collagen metabolic process', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(179639, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0107261', 'abnormal dorsal-ventral axis', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(179640, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0141264', 'abnormal schooling behavior', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(179641, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0128000', 'absent behavior', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(179642, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0141790', 'abnormal cellular metabolic process', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(179643, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0141791', 'abnormal primary metabolic process', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(179644, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0100638', 'abnormal polar body', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(179645, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0101333', 'abnormal barrier epithelial cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(179646, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0133388', 'absent insulin receptor signaling pathway', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(179647, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0141600', 'absent metamorphosis', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(179648, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0100031', 'abnormal central nervous system', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(179649, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0101435', 'abnormal paracrine cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(179650, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0131691', 'abnormal molecular function', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(179651, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0141860', 'abnormal malate-aspartate shuttle', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(179652, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0141777', 'abnormal catabolic process', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(179653, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0100232', 'abnormal lymphatic system', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(179654, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0141770', 'abnormal urate homeostasis', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(179655, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0107312', 'abnormal filopodium', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(179656, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0101468', 'abnormal stage I oocyte', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(179657, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0141499', 'abnormal tadpole', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(179658, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0101157', 'abnormal female organism', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(179659, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0100289', 'abnormal chondroblast', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(179660, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0141795', 'abnormal glycosylation', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(179661, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0100691', 'abnormal keratin accumulating cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(179662, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0100437', 'abnormal proepicardium', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(179663, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0101071', 'abnormal endoplasmic reticulum', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(179664, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0131469', 'abnormal heart process', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(179665, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0101113', 'abnormal stage IV oocyte', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(179666, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0116434', 'abnormal biological process', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(179667, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0141781', 'abnormal secondary metabolic process', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(179668, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0115505', 'dead whole organism', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(179669, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0100888', 'abnormal microtubule', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(179670, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0101061', 'abnormal plasma membrane', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(179671, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0141809', 'abnormal catalytic activity', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(179672, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0141907', 'abnormal putrescine metabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(179673, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0131745', 'abnormal axis elongation', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(179674, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0101409', 'abnormal perivitelline space', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(179675, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0101221', 'abnormal larval immune system', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(179676, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0101264', 'abnormal mitotic spindle', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(179677, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0141904', 'abnormal glucosamine metabolic process', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(179678, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0100032', 'abnormal nervous system', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(179679, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0100481', 'abnormal anatomical line', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(179680, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0131725', 'abnormal phosphorylation of RNA polymerase II C-terminal domain', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(179681, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0100674', 'abnormal secondary oogonium', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(179682, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0100337', 'abnormal zygote', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(179683, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0141272', 'absent surface breathing', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(179684, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0100515', 'abnormal somatic stem cell', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(179685, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0141771', 'abnormal urea homeostasis', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(179686, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0100894', 'abnormal nucleus', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(179687, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0141748', 'abnormal gas homeostasis', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(179688, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0141784', 'abnormal cellular hormone metabolic process', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(179689, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0101461', 'abnormal sperm entry point', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(179690, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0100728', 'abnormal cell condensation', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(179691, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0100392', 'abnormal cilium', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(179692, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0101448', 'abnormal myelin accumulating cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(179693, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0131675', 'abnormal spindle microtubule', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(179694, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0141892', 'abnormal inositol metabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(179695, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0141743', 'abnormal chemical homeostasis within a tissue', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(179696, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0100026', 'abnormal germ cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(179697, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0141787', 'abnormal hormone metabolic process', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(179698, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0107262', 'abnormal left-right axis', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(179699, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0100501', 'abnormal urogenital system', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(179700, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0141754', 'abnormal homeostatic process', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(179701, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0141786', 'abnormal pigment metabolic process', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(179702, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0100239', 'abnormal acellular anatomical structure', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(179703, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0101373', 'abnormal oxygen accumulating cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(179704, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0100344', 'abnormal portion of organism substance', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(179705, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0100969', 'abnormal disaggregated/reaggregated ectoderm treated with activin', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(179706, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0131666', 'abnormal adherens junction', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(179707, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0101110', 'abnormal cell-free extract', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(179708, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0100976', 'abnormal multiciliated cell', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(179709, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0100653', 'abnormal myoblast', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(179710, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0141794', 'abnormal prosthetic group metabolic process', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(179711, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0100172', 'abnormal stem cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(179712, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0101109', 'abnormal egg cell-free extract', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(179713, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0100010', 'abnormal multicellular anatomical structure', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(179714, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0101004', 'abnormal acid secreting cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(179715, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0101366', 'abnormal morula cell', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(179716, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0115508', 'abnormally peramorphic growth of whole organism', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(179717, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0141798', 'abnormal lipid metabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(179718, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0141792', 'abnormal small molecule metabolic process', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(179719, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0100084', 'abnormal anatomical group', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(179720, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0100626', 'abnormal primordial germ cell', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(179721, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0115512', 'abnormally semi-erect whole organism', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(179722, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0100062', 'abnormal anatomical space', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(179723, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0100006', 'abnormal anatomical structure', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(179724, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0131729', 'abnormal regulation of growth rate', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(179725, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0141267', 'abnormal resting posture', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(179726, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0131685', 'abnormal cortical actin cytoskeleton', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(179727, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0141263', 'abnormal visually guided collision avoidance behavior', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(179728, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0100852', 'abnormal interdigital region', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(179729, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0107259', 'abnormal animal-vegetal axis', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(179730, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0101297', 'abnormal barrier cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(179731, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0100176', 'abnormal stage VI oocyte', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(179732, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0100917', 'abnormal stage III oocyte', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(179733, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0100585', 'abnormal elastica externa', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(179734, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0141775', 'abnormal nitrogen compound metabolic process', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(179735, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0101237', 'abnormal mucus secreting cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(179736, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0141266', 'abnormal surface breathing', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(179737, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0100081', 'abnormal anatomical entity in vitro', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(179738, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0100372', 'abnormal hematological system', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(179739, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0141276', 'decreased surface breathing', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(179740, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0100546', 'abnormal whole organism', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(179741, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0100025', 'abnormal oocyte', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(179742, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0141776', 'abnormal metabolic process', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(179743, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0115509', 'abnormally semi-viable whole organism', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(179744, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0100573', 'abnormal extraembryonic structure', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(179745, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0101220', 'abnormal centriole', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(179746, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0100377', 'abnormal connective tissue', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(179747, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0101132', 'abnormal apoptotic cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(179748, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0116494', 'absent biological process', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(179749, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0100317', 'abnormal respiratory system', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(179750, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0131730', 'abnormal regulation of protein folding', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(179751, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0101228', 'abnormal mesenchymal stem cell', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(179752, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0141796', 'abnormal demethylation', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(179753, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0101547', 'abnormal lampbrush chromosome', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(179754, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0141271', 'increased surface breathing', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(179755, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0100225', 'abnormal endocrine system', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(179756, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0100549', 'abnormal mitotic cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(179757, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0100004', 'abnormal cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(179758, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0100308', 'abnormal early embryonic cell', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(179759, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0101513', 'abnormal basal body', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(179760, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0100956', 'abnormal centrosome', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(179761, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0100258', 'abnormal organ part', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(179762, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0107258', 'abnormal anatomical axis', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(179763, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0107270', 'abnormal proximal-distal axis', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(179764, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0107284', 'abnormal migrating myoblast', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(179765, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0131677', 'abnormal actin filament', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(179766, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0100429', 'abnormal spermatid', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(179767, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0100274', 'abnormal sensory system', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(179768, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0100202', 'abnormal embryo', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(179769, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0100599', 'abnormal adult immune system', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(179770, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0100545', 'abnormal male organism', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(179771, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0101141', 'abnormal Keller explant', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(179772, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0100899', 'abnormal secondary spermatogonium', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(179773, 'HP:0033771', 'Pleuritic chest pain', 'XPO:0141265', 'abnormal escape behavior', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(179774, 'HP:0010249', 'Enlarged epiphyses of the distal phalanges of the hand', 'XPO:0103755', 'increased size of the forelimb digit', 0.4166666666666667, 7.492661022682715, 1.7669018345070744, 'HP:0001167', 'Abnormal finger morphology'),
(179775, 'HP:0010249', 'Enlarged epiphyses of the distal phalanges of the hand', 'XPO:0130664', 'increased size of the forelimb digit 2', 0.4065040650406504, 7.492661022682715, 1.7452212363170925, 'HP:0001167', 'Abnormal finger morphology'),
(179776, 'HP:0010249', 'Enlarged epiphyses of the distal phalanges of the hand', 'XPO:0115789', 'duplicated forelimb digit 5 in regenerating forelimb', 0.41605839416058393, 7.774297771301195, 1.7984887673971672, 'HP:0005918', 'Abnormal finger phalanx morphology'),
(179777, 'HP:0010249', 'Enlarged epiphyses of the distal phalanges of the hand', 'XPO:0130624', 'increased size of the forelimb digit 4', 0.4065040650406504, 7.492661022682715, 1.7452212363170925, 'HP:0001167', 'Abnormal finger morphology'),
(179778, 'HP:0010249', 'Enlarged epiphyses of the distal phalanges of the hand', 'XPO:0102746', 'abnormal forelimb digit 2 morphology', 0.40869565217391307, 7.492661022682715, 1.7499194219115835, 'HP:0001167', 'Abnormal finger morphology'),
(179779, 'HP:0010249', 'Enlarged epiphyses of the distal phalanges of the hand', 'XPO:0115788', 'duplicated forelimb digit 4 in regenerating forelimb', 0.41605839416058393, 7.774297771301195, 1.7984887673971672, 'HP:0005918', 'Abnormal finger phalanx morphology'),
(179780, 'HP:0010249', 'Enlarged epiphyses of the distal phalanges of the hand', 'XPO:0102787', 'abnormal forelimb digit 5 morphology', 0.40869565217391307, 7.492661022682715, 1.7499194219115835, 'HP:0001167', 'Abnormal finger morphology'),
(179781, 'HP:0010249', 'Enlarged epiphyses of the distal phalanges of the hand', 'XPO:0115786', 'duplicated forelimb digit 2 in regenerating forelimb', 0.41605839416058393, 7.774297771301195, 1.7984887673971672, 'HP:0005918', 'Abnormal finger phalanx morphology'),
(179782, 'HP:0010249', 'Enlarged epiphyses of the distal phalanges of the hand', 'XPO:0129652', 'increased size of the forelimb digit 3', 0.4065040650406504, 7.492661022682715, 1.7452212363170925, 'HP:0001167', 'Abnormal finger morphology'),
(179783, 'HP:0010249', 'Enlarged epiphyses of the distal phalanges of the hand', 'XPO:0130637', 'increased size of the forelimb digit 5', 0.4065040650406504, 7.492661022682715, 1.7452212363170925, 'HP:0001167', 'Abnormal finger morphology'),
(179784, 'HP:0010249', 'Enlarged epiphyses of the distal phalanges of the hand', 'XPO:0102214', 'abnormal forelimb digit morphology', 0.415929203539823, 7.492661022682715, 1.7653375120804229, 'HP:0001167', 'Abnormal finger morphology'),
(179785, 'HP:0010249', 'Enlarged epiphyses of the distal phalanges of the hand', 'XPO:0102529', 'abnormal forelimb digit 4 morphology', 0.40869565217391307, 7.492661022682715, 1.7499194219115835, 'HP:0001167', 'Abnormal finger morphology'),
(179786, 'HP:0010249', 'Enlarged epiphyses of the distal phalanges of the hand', 'XPO:0115787', 'duplicated forelimb digit 3 in regenerating forelimb', 0.41605839416058393, 7.774297771301195, 1.7984887673971672, 'HP:0005918', 'Abnormal finger phalanx morphology'),
(179787, 'HP:0010249', 'Enlarged epiphyses of the distal phalanges of the hand', 'XPO:0103634', 'abnormally increased number of forelimb digit', 0.4523809523809524, 7.774297771301195, 1.875351761636827, 'HP:0005918', 'Abnormal finger phalanx morphology'),
(179788, 'HP:0010249', 'Enlarged epiphyses of the distal phalanges of the hand', 'XPO:0102598', 'abnormal forelimb digit 3 morphology', 0.40869565217391307, 7.492661022682715, 1.7499194219115835, 'HP:0001167', 'Abnormal finger morphology'),
(179789, 'HP:0010249', 'Enlarged epiphyses of the distal phalanges of the hand', 'XPO:0103609', 'abnormally increased number of forelimb digit in the regenerating forelimb', 0.4318181818181818, 7.774297771301195, 1.8322344633033256, 'HP:0005918', 'Abnormal finger phalanx morphology'),
(179790, 'HP:0011410', 'Caesarian section', 'XPO:0100207', 'abnormal blastema', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(179791, 'HP:0011410', 'Caesarian section', 'XPO:0100282', 'abnormal pelvic girdle primordium', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(179792, 'HP:0011410', 'Caesarian section', 'XPO:0141718', 'abnormal posterior notochord', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(179793, 'HP:0011410', 'Caesarian section', 'XPO:0141860', 'abnormal malate-aspartate shuttle', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(179794, 'HP:0011410', 'Caesarian section', 'XPO:0100192', 'abnormal epithelium', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(179795, 'HP:0011410', 'Caesarian section', 'XPO:0101450', 'abnormal myeloid cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(179796, 'HP:0011410', 'Caesarian section', 'XPO:0100976', 'abnormal multiciliated cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(179797, 'HP:0011410', 'Caesarian section', 'XPO:0100653', 'abnormal myoblast', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(179798, 'HP:0011410', 'Caesarian section', 'XPO:0107311', 'abnormal apical junction complex', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(179799, 'HP:0011410', 'Caesarian section', 'XPO:0100151', 'abnormal primordium', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(179800, 'HP:0011410', 'Caesarian section', 'XPO:0141797', 'abnormal hydrogen metabolic process', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(179801, 'HP:0011410', 'Caesarian section', 'XPO:0107271', 'abnormal apical region', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(179802, 'HP:0011410', 'Caesarian section', 'XPO:0101240', 'abnormal ciliated non-epidermal cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(179803, 'HP:0011410', 'Caesarian section', 'XPO:0100437', 'abnormal proepicardium', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(179804, 'HP:0011410', 'Caesarian section', 'XPO:0100916', 'abnormal principal cavity', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(179805, 'HP:0011410', 'Caesarian section', 'XPO:0100728', 'abnormal cell condensation', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(179806, 'HP:0011410', 'Caesarian section', 'XPO:0100309', 'abnormal vegetal hemisphere', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(179807, 'HP:0011410', 'Caesarian section', 'XPO:0100417', 'abnormal dense regular connective tissue', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(179808, 'HP:0011410', 'Caesarian section', 'XPO:0101406', 'abnormal cleavage furrow', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(179809, 'HP:0011410', 'Caesarian section', 'XPO:0101237', 'abnormal mucus secreting cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(179810, 'HP:0011410', 'Caesarian section', 'XPO:0100501', 'abnormal urogenital system', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(179811, 'HP:0011410', 'Caesarian section', 'XPO:0101569', 'abnormal activin-induced ectoderm', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(179812, 'HP:0011410', 'Caesarian section', 'XPO:0141777', 'abnormal catabolic process', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(179813, 'HP:0011410', 'Caesarian section', 'XPO:0142054', 'abnormal digestive tract', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(179814, 'HP:0011410', 'Caesarian section', 'XPO:0100014', 'abnormal tissue', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(179815, 'HP:0011410', 'Caesarian section', 'XPO:0100999', 'abnormal serous membrane', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(179816, 'HP:0011410', 'Caesarian section', 'XPO:0100232', 'abnormal lymphatic system', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(179817, 'HP:0011410', 'Caesarian section', 'XPO:0100023', 'abnormal mesenchyme', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(179818, 'HP:0011410', 'Caesarian section', 'XPO:0100231', 'abnormal compound organ', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(179819, 'HP:0011410', 'Caesarian section', 'XPO:0107259', 'abnormal animal-vegetal axis', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(179820, 'HP:0011410', 'Caesarian section', 'XPO:0131691', 'abnormal molecular function', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(179821, 'HP:0011410', 'Caesarian section', 'XPO:0141271', 'increased surface breathing', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(179822, 'HP:0011410', 'Caesarian section', 'XPO:0101110', 'abnormal cell-free extract', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(179823, 'HP:0011410', 'Caesarian section', 'XPO:0100762', 'abnormal intersomitic region', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(179824, 'HP:0011410', 'Caesarian section', 'XPO:0100114', 'abnormal peripheral nervous system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(179825, 'HP:0011410', 'Caesarian section', 'XPO:0107273', 'abnormal basal region', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(179826, 'HP:0011410', 'Caesarian section', 'XPO:0101168', 'abnormal circulating cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(179827, 'HP:0011410', 'Caesarian section', 'XPO:0100296', 'abnormal tail region', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(179828, 'HP:0011410', 'Caesarian section', 'XPO:0100907', 'abnormal cytoplasm', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(179829, 'HP:0011410', 'Caesarian section', 'XPO:0100307', 'abnormal blastomere', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(179830, 'HP:0011410', 'Caesarian section', 'XPO:0100277', 'abnormal blastocoel', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(179831, 'HP:0011410', 'Caesarian section', 'XPO:0141783', 'abnormal collagen metabolic process', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(179832, 'HP:0011410', 'Caesarian section', 'XPO:0141782', 'abnormal methylation', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(179833, 'HP:0011410', 'Caesarian section', 'XPO:0100006', 'abnormal anatomical structure', 0.5294117647058824, 1.706362323152461, 0.9504568842024205, 'UPHENO:0002536', 'abnormal anatomical entity'),
(179834, 'HP:0011410', 'Caesarian section', 'XPO:0100511', 'abnormal stylopod', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(179835, 'HP:0011410', 'Caesarian section', 'XPO:0100638', 'abnormal polar body', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(179836, 'HP:0011410', 'Caesarian section', 'XPO:0101467', 'abnormal alkali secreting cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(179837, 'HP:0011410', 'Caesarian section', 'XPO:0100533', 'abnormal melanoblast', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(179838, 'HP:0011410', 'Caesarian section', 'XPO:0100858', 'abnormal presumptive midbrain-hindbrain boundary', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(179839, 'HP:0011410', 'Caesarian section', 'XPO:0100890', 'abnormal pharyngeal cavity', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(179840, 'HP:0011410', 'Caesarian section', 'XPO:0100574', 'abnormal gastrula cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(179841, 'HP:0011410', 'Caesarian section', 'XPO:0107272', 'abnormal axial region', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(179842, 'HP:0011410', 'Caesarian section', 'XPO:0101498', 'abnormal stage II oocyte', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(179843, 'HP:0011410', 'Caesarian section', 'XPO:0100887', 'abnormal right-dorsal blastomere', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(179844, 'HP:0011410', 'Caesarian section', 'XPO:0100256', 'abnormal paired appendage', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(179845, 'HP:0011410', 'Caesarian section', 'XPO:0100103', 'abnormal trunk', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(179846, 'HP:0011410', 'Caesarian section', 'XPO:0131725', 'abnormal phosphorylation of RNA polymerase II C-terminal domain', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(179847, 'HP:0011410', 'Caesarian section', 'XPO:0101004', 'abnormal acid secreting cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(179848, 'HP:0011410', 'Caesarian section', 'XPO:0100402', 'abnormal zeugopod', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(179849, 'HP:0011410', 'Caesarian section', 'XPO:0101157', 'abnormal female organism', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(179850, 'HP:0011410', 'Caesarian section', 'XPO:0100722', 'abnormal barbel', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(179851, 'HP:0011410', 'Caesarian section', 'XPO:0100862', 'abnormal blastomere V1', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(179852, 'HP:0011410', 'Caesarian section', 'XPO:0141272', 'absent surface breathing', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(179853, 'HP:0011410', 'Caesarian section', 'XPO:0101096', 'abnormal tendon', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(179854, 'HP:0011410', 'Caesarian section', 'XPO:0100599', 'abnormal adult immune system', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(179855, 'HP:0011410', 'Caesarian section', 'XPO:0100067', 'abnormal animal hemisphere', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(179856, 'HP:0011410', 'Caesarian section', 'XPO:0100802', 'abnormal exocrine cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(179857, 'HP:0011410', 'Caesarian section', 'XPO:0100249', 'abnormal avascular GAG-rich matrix', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(179858, 'HP:0011410', 'Caesarian section', 'XPO:0100484', 'abnormal cement gland primordium', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(179859, 'HP:0011410', 'Caesarian section', 'XPO:0100989', 'abnormal right blastomere', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(179860, 'HP:0011410', 'Caesarian section', 'XPO:0141771', 'abnormal urea homeostasis', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(179861, 'HP:0011410', 'Caesarian section', 'XPO:0101029', 'abnormal right spleen primordium', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(179862, 'HP:0011410', 'Caesarian section', 'XPO:0101092', 'abnormal dorso-lateral marginal zone', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(179863, 'HP:0011410', 'Caesarian section', 'XPO:0100573', 'abnormal extraembryonic structure', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(179864, 'HP:0011410', 'Caesarian section', 'XPO:0100702', 'abnormal glial cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(179865, 'HP:0011410', 'Caesarian section', 'XPO:0142051', 'abnormal cerebrospinal fluid', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(179866, 'HP:0011410', 'Caesarian section', 'XPO:0107253', 'abnormal enteric nervous system', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(179867, 'HP:0011410', 'Caesarian section', 'XPO:0100856', 'abnormal simple organ', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(179868, 'HP:0011410', 'Caesarian section', 'XPO:0100842', 'abnormal left-dorsal blastomere', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(179869, 'HP:0011410', 'Caesarian section', 'XPO:0101074', 'abnormal germinal vesicle', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(179870, 'HP:0011410', 'Caesarian section', 'XPO:0100807', 'abnormal matrix-based tissue', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(179871, 'HP:0011410', 'Caesarian section', 'XPO:0100205', 'abnormal limb segment', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(179872, 'HP:0011410', 'Caesarian section', 'XPO:0107285', 'abnormal flexural organ', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(179873, 'HP:0011410', 'Caesarian section', 'XPO:0100745', 'abnormal anterior lymph sac', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(179874, 'HP:0011410', 'Caesarian section', 'XPO:0107276', 'abnormal dorsal region', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(179875, 'HP:0011410', 'Caesarian section', 'XPO:0100274', 'abnormal sensory system', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(179876, 'HP:0011410', 'Caesarian section', 'XPO:0101333', 'abnormal barrier epithelial cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(179877, 'HP:0011410', 'Caesarian section', 'XPO:0141266', 'abnormal surface breathing', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(179878, 'HP:0011410', 'Caesarian section', 'XPO:0101366', 'abnormal morula cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(179879, 'HP:0011410', 'Caesarian section', 'XPO:0100261', 'abnormal multilaminar epithelium', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(179880, 'HP:0011410', 'Caesarian section', 'XPO:0100392', 'abnormal cilium', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(179881, 'HP:0011410', 'Caesarian section', 'XPO:0100031', 'abnormal central nervous system', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(179882, 'HP:0011410', 'Caesarian section', 'XPO:0100899', 'abnormal secondary spermatogonium', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(179883, 'HP:0011410', 'Caesarian section', 'XPO:0141794', 'abnormal prosthetic group metabolic process', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(179884, 'HP:0011410', 'Caesarian section', 'XPO:0100268', 'abnormal circulatory system', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(179885, 'HP:0011410', 'Caesarian section', 'XPO:0107258', 'abnormal anatomical axis', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(179886, 'HP:0011410', 'Caesarian section', 'XPO:0100557', 'abnormal prime meridian', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(179887, 'HP:0011410', 'Caesarian section', 'XPO:0100537', 'abnormal medium cavity', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(179888, 'HP:0011410', 'Caesarian section', 'XPO:0107268', 'abnormal left side', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(179889, 'HP:0011410', 'Caesarian section', 'XPO:0101638', 'abnormal anatomical structure morphology', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(179890, 'HP:0011410', 'Caesarian section', 'XPO:0101264', 'abnormal mitotic spindle', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(179891, 'HP:0011410', 'Caesarian section', 'XPO:0101113', 'abnormal stage IV oocyte', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(179892, 'HP:0011410', 'Caesarian section', 'XPO:0115391', 'abnormally undifferentiated alimentary system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(179893, 'HP:0011410', 'Caesarian section', 'XPO:0100852', 'abnormal interdigital region', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(179894, 'HP:0011410', 'Caesarian section', 'XPO:0101472', 'abnormal zygote cortex', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(179895, 'HP:0011410', 'Caesarian section', 'XPO:0107261', 'abnormal dorsal-ventral axis', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(179896, 'HP:0011410', 'Caesarian section', 'XPO:0100172', 'abnormal stem cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(179897, 'HP:0011410', 'Caesarian section', 'XPO:0141745', 'abnormal creatinine homeostasis', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(179898, 'HP:0011410', 'Caesarian section', 'XPO:0101535', 'abnormal absorptive cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(179899, 'HP:0011410', 'Caesarian section', 'XPO:0115505', 'dead whole organism', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(179900, 'HP:0011410', 'Caesarian section', 'XPO:0131675', 'abnormal spindle microtubule', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(179901, 'HP:0011410', 'Caesarian section', 'XPO:0100429', 'abnormal spermatid', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(179902, 'HP:0011410', 'Caesarian section', 'XPO:0101468', 'abnormal stage I oocyte', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(179903, 'HP:0011410', 'Caesarian section', 'XPO:0101448', 'abnormal myelin accumulating cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(179904, 'HP:0011410', 'Caesarian section', 'XPO:0100900', 'abnormal angioblast', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(179905, 'HP:0011410', 'Caesarian section', 'XPO:0100378', 'abnormal perichondrium', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(179906, 'HP:0011410', 'Caesarian section', 'XPO:0100026', 'abnormal germ cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(179907, 'HP:0011410', 'Caesarian section', 'XPO:0100415', 'abnormal secretory epithelial cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(179908, 'HP:0011410', 'Caesarian section', 'XPO:0100482', 'abnormal Mullerian duct', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(179909, 'HP:0011410', 'Caesarian section', 'XPO:0141784', 'abnormal cellular hormone metabolic process', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(179910, 'HP:0011410', 'Caesarian section', 'XPO:0100203', 'abnormal endocrine cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(179911, 'HP:0011410', 'Caesarian section', 'XPO:0100800', 'abnormal ventral marginal zone', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(179912, 'HP:0011410', 'Caesarian section', 'XPO:0141497', 'abnormal lymphoblast', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(179913, 'HP:0011410', 'Caesarian section', 'XPO:0101543', 'abnormal external gill', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(179914, 'HP:0011410', 'Caesarian section', 'XPO:0100196', 'abnormal neuron', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(179915, 'HP:0011410', 'Caesarian section', 'XPO:0100060', 'abnormal regenerating tissue', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(179916, 'HP:0011410', 'Caesarian section', 'XPO:0101302', 'abnormal subcortical cytoplasm', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(179917, 'HP:0011410', 'Caesarian section', 'XPO:0100081', 'abnormal anatomical entity in vitro', 0.5294117647058824, 1.706362323152461, 0.9504568842024205, 'UPHENO:0002536', 'abnormal anatomical entity'),
(179918, 'HP:0011410', 'Caesarian section', 'XPO:0100009', 'abnormal multi-tissue structure', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(179919, 'HP:0011410', 'Caesarian section', 'XPO:0100265', 'abnormal sensory epithelial cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(179920, 'HP:0011410', 'Caesarian section', 'XPO:0100383', 'abnormal amputated fin', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(179921, 'HP:0011410', 'Caesarian section', 'XPO:0100551', 'abnormal oocyte cortex', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(179922, 'HP:0011410', 'Caesarian section', 'XPO:0101362', 'abnormal vegetal cortex', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(179923, 'HP:0011410', 'Caesarian section', 'XPO:0101200', 'abnormal joint region', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(179924, 'HP:0011410', 'Caesarian section', 'XPO:0107339', 'abnormal yolk platelet', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(179925, 'HP:0011410', 'Caesarian section', 'XPO:0141743', 'abnormal chemical homeostasis within a tissue', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(179926, 'HP:0011410', 'Caesarian section', 'XPO:0100588', 'abnormal unicellular gland', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(179927, 'HP:0011410', 'Caesarian section', 'XPO:0100781', 'abnormal presumptive ectoderm', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(179928, 'HP:0011410', 'Caesarian section', 'XPO:0100372', 'abnormal hematological system', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(179929, 'HP:0011410', 'Caesarian section', 'XPO:0100545', 'abnormal male organism', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(179930, 'HP:0011410', 'Caesarian section', 'XPO:0131667', 'abnormal actin cytoskeleton', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(179931, 'HP:0011410', 'Caesarian section', 'XPO:0101411', 'abnormal marginal zone (sensu neural)', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(179932, 'HP:0011410', 'Caesarian section', 'XPO:0100547', 'abnormal blastomere V2', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(179933, 'HP:0011410', 'Caesarian section', 'XPO:0100854', 'abnormal spiracle', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(179934, 'HP:0011410', 'Caesarian section', 'XPO:0100846', 'abnormal hindlimb', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(179935, 'HP:0011410', 'Caesarian section', 'XPO:0101575', 'abnormal vitelline membrane', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(179936, 'HP:0011410', 'Caesarian section', 'XPO:0100515', 'abnormal somatic stem cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(179937, 'HP:0011410', 'Caesarian section', 'XPO:0101023', 'abnormal ultimobranchial body', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(179938, 'HP:0011410', 'Caesarian section', 'XPO:0100691', 'abnormal keratin accumulating cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(179939, 'HP:0011410', 'Caesarian section', 'XPO:0100642', 'abnormal gustatory system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(179940, 'HP:0011410', 'Caesarian section', 'XPO:0101072', 'abnormal mitochondrial cloud', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(179941, 'HP:0011410', 'Caesarian section', 'XPO:0142057', 'abnormal desmosome', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(179942, 'HP:0011410', 'Caesarian section', 'XPO:0100912', 'abnormal trabecula', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(179943, 'HP:0011410', 'Caesarian section', 'XPO:0101176', 'abnormal non-ciliated epithelial cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(179944, 'HP:0011410', 'Caesarian section', 'XPO:0100295', 'abnormal extracellular matrix', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(179945, 'HP:0011410', 'Caesarian section', 'XPO:0101501', 'abnormal parabrachial area', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(179946, 'HP:0011410', 'Caesarian section', 'XPO:0131677', 'abnormal actin filament', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(179947, 'HP:0011410', 'Caesarian section', 'XPO:0100377', 'abnormal connective tissue', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(179948, 'HP:0011410', 'Caesarian section', 'XPO:0100202', 'abnormal embryo', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(179949, 'HP:0011410', 'Caesarian section', 'XPO:0100465', 'abnormal skeletal system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(179950, 'HP:0011410', 'Caesarian section', 'XPO:0142056', 'abnormal main body axis', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(179951, 'HP:0011410', 'Caesarian section', 'XPO:0101349', 'abnormal trunk region', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(179952, 'HP:0011410', 'Caesarian section', 'XPO:0101149', 'abnormal amputated limb', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(179953, 'HP:0011410', 'Caesarian section', 'XPO:0101587', 'abnormal hemangioblast', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(179954, 'HP:0011410', 'Caesarian section', 'XPO:0100784', 'abnormal left blastomere', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(179955, 'HP:0011410', 'Caesarian section', 'XPO:0100493', 'abnormal liver and biliary system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(179956, 'HP:0011410', 'Caesarian section', 'XPO:0115509', 'abnormally semi-viable whole organism', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(179957, 'HP:0011410', 'Caesarian section', 'XPO:0100742', 'abnormal musculoskeletal system', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(179958, 'HP:0011410', 'Caesarian section', 'XPO:0100176', 'abnormal stage VI oocyte', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(179959, 'HP:0011410', 'Caesarian section', 'XPO:0107270', 'abnormal proximal-distal axis', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(179960, 'HP:0011410', 'Caesarian section', 'XPO:0100468', 'abnormal muscular system', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(179961, 'HP:0011410', 'Caesarian section', 'XPO:0101553', 'abnormal dental epithelium', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(179962, 'HP:0011410', 'Caesarian section', 'XPO:0101220', 'abnormal centriole', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(179963, 'HP:0011410', 'Caesarian section', 'XPO:0100393', 'abnormal involuting marginal zone', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(179964, 'HP:0011410', 'Caesarian section', 'XPO:0100640', 'abnormal notochordal sheath', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(179965, 'HP:0011410', 'Caesarian section', 'XPO:0100164', 'abnormal neural nucleus', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(179966, 'HP:0011410', 'Caesarian section', 'XPO:0100643', 'abnormal thoracic region', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(179967, 'HP:0011410', 'Caesarian section', 'XPO:0100667', 'abnormal vegetal yolk mass', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(179968, 'HP:0011410', 'Caesarian section', 'XPO:0100175', 'abnormal migrating neuroblast', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(179969, 'HP:0011410', 'Caesarian section', 'XPO:0141772', 'abnormal water homeostasis', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(179970, 'HP:0011410', 'Caesarian section', 'XPO:0107288', 'abnormal larval alimentary system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(179971, 'HP:0011410', 'Caesarian section', 'XPO:0141315', 'abnormal anatomical region', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(179972, 'HP:0011410', 'Caesarian section', 'XPO:0100969', 'abnormal disaggregated/reaggregated ectoderm treated with activin', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(179973, 'HP:0011410', 'Caesarian section', 'XPO:0100104', 'abnormal embryonic structure', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(179974, 'HP:0011410', 'Caesarian section', 'XPO:0100084', 'abnormal anatomical group', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(179975, 'HP:0011410', 'Caesarian section', 'XPO:0100002', 'abnormal head', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(179976, 'HP:0011410', 'Caesarian section', 'XPO:0101283', 'abnormal left-ventral blastomere', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(179977, 'HP:0011410', 'Caesarian section', 'XPO:0131685', 'abnormal cortical actin cytoskeleton', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(179978, 'HP:0011410', 'Caesarian section', 'XPO:0101573', 'abnormal peripheral vegetal yolk mass', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(179979, 'HP:0011410', 'Caesarian section', 'XPO:0101061', 'abnormal plasma membrane', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(179980, 'HP:0011410', 'Caesarian section', 'XPO:0100868', 'abnormal transporting epithelium', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(179981, 'HP:0011410', 'Caesarian section', 'XPO:0100610', 'abnormal appendage', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(179982, 'HP:0011410', 'Caesarian section', 'XPO:0100449', 'abnormal lymphocyte', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(179983, 'HP:0011410', 'Caesarian section', 'XPO:0107269', 'abnormal right side', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(179984, 'HP:0011410', 'Caesarian section', 'XPO:0141267', 'abnormal resting posture', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(179985, 'HP:0011410', 'Caesarian section', 'XPO:0101451', 'abnormal dorsal lymph space', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(179986, 'HP:0011410', 'Caesarian section', 'XPO:0100549', 'abnormal mitotic cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(179987, 'HP:0011410', 'Caesarian section', 'XPO:0100386', 'abnormal limb', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(179988, 'HP:0011410', 'Caesarian section', 'XPO:0141904', 'abnormal glucosamine metabolic process', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(179989, 'HP:0011410', 'Caesarian section', 'XPO:0107266', 'abnormal dorsal side', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(179990, 'HP:0011410', 'Caesarian section', 'XPO:0100888', 'abnormal microtubule', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(179991, 'HP:0011410', 'Caesarian section', 'XPO:0107284', 'abnormal migrating myoblast', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(179992, 'HP:0011410', 'Caesarian section', 'XPO:0100363', 'abnormal cardiovascular system', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(179993, 'HP:0011410', 'Caesarian section', 'XPO:0100816', 'abnormal blastocoel anlage', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(179994, 'HP:0011410', 'Caesarian section', 'XPO:0131687', 'abnormal astral microtubule', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(179995, 'HP:0011410', 'Caesarian section', 'XPO:0100384', 'abnormal amputated tissue', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(179996, 'HP:0011410', 'Caesarian section', 'XPO:0100605', 'abnormal prechordal plate', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(179997, 'HP:0011410', 'Caesarian section', 'XPO:0100915', 'abnormal dermal system', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(179998, 'HP:0011410', 'Caesarian section', 'XPO:0141778', 'abnormal biosynthetic process', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(179999, 'HP:0011410', 'Caesarian section', 'XPO:0115758', 'abnormally decreased mobility of melanoblast', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(180000, 'HP:0011410', 'Caesarian section', 'XPO:0101513', 'abnormal basal body', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(180001, 'HP:0011410', 'Caesarian section', 'XPO:0100416', 'abnormal ligament', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(180002, 'HP:0011410', 'Caesarian section', 'XPO:0101221', 'abnormal larval immune system', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(180003, 'HP:0011410', 'Caesarian section', 'XPO:0101463', 'abnormal right-ventral blastomere', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(180004, 'HP:0011410', 'Caesarian section', 'XPO:0101212', 'abnormal glomeral mesenchyme', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(180005, 'HP:0011410', 'Caesarian section', 'XPO:0101071', 'abnormal endoplasmic reticulum', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(180006, 'HP:0011410', 'Caesarian section', 'XPO:0101297', 'abnormal barrier cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(180007, 'HP:0011410', 'Caesarian section', 'XPO:0100108', 'abnormal cell part', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(180008, 'HP:0011410', 'Caesarian section', 'XPO:0100186', 'abnormal uveal tract', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(180009, 'HP:0011410', 'Caesarian section', 'XPO:0131666', 'abnormal adherens junction', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(180010, 'HP:0011410', 'Caesarian section', 'XPO:0100152', 'abnormal alimentary system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(180011, 'HP:0011410', 'Caesarian section', 'XPO:0101040', 'abnormal axial mesoderm', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(180012, 'HP:0011410', 'Caesarian section', 'XPO:0107260', 'abnormal anterior-posterior axis', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(180013, 'HP:0011410', 'Caesarian section', 'XPO:0100010', 'abnormal multicellular anatomical structure', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(180014, 'HP:0011410', 'Caesarian section', 'XPO:0100917', 'abnormal stage III oocyte', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(180015, 'HP:0011410', 'Caesarian section', 'XPO:0100337', 'abnormal zygote', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(180016, 'HP:0011410', 'Caesarian section', 'XPO:0141265', 'abnormal escape behavior', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(180017, 'HP:0011410', 'Caesarian section', 'XPO:0141715', 'abnormal septum', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(180018, 'HP:0011410', 'Caesarian section', 'XPO:0100727', 'abnormal odontogenic papilla', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(180019, 'HP:0011410', 'Caesarian section', 'XPO:0101326', 'abnormal cementoblast', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(180020, 'HP:0011410', 'Caesarian section', 'XPO:0101311', 'abnormal bottle cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(180021, 'HP:0011410', 'Caesarian section', 'XPO:0100587', 'abnormal vestibuloauditory system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(180022, 'HP:0011410', 'Caesarian section', 'XPO:0101099', 'abnormal ventro-lateral marginal zone', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(180023, 'HP:0011410', 'Caesarian section', 'XPO:0100339', 'abnormal circumblastoporal collar', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(180024, 'HP:0011410', 'Caesarian section', 'XPO:0101409', 'abnormal perivitelline space', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(180025, 'HP:0011410', 'Caesarian section', 'XPO:0131723', 'abnormal pathway-restricted SMAD protein phosphorylation', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(180026, 'HP:0011410', 'Caesarian section', 'XPO:0116494', 'absent biological process', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(180027, 'HP:0011410', 'Caesarian section', 'XPO:0100025', 'abnormal oocyte', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(180028, 'HP:0011410', 'Caesarian section', 'XPO:0116434', 'abnormal biological process', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(180029, 'HP:0011410', 'Caesarian section', 'XPO:0101174', 'abnormal articular system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(180030, 'HP:0011410', 'Caesarian section', 'XPO:0100069', 'abnormal urinary system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(180031, 'HP:0011410', 'Caesarian section', 'XPO:0101010', 'abnormal dorsal marginal zone', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(180032, 'HP:0011410', 'Caesarian section', 'XPO:0141841', 'abnormality of whole organism mass', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(180033, 'HP:0011410', 'Caesarian section', 'XPO:0141792', 'abnormal small molecule metabolic process', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(180034, 'HP:0011410', 'Caesarian section', 'XPO:0141264', 'abnormal schooling behavior', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(180035, 'HP:0011410', 'Caesarian section', 'XPO:0107278', 'abnormal medial region', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(180036, 'HP:0011410', 'Caesarian section', 'XPO:0101519', 'abnormal hypobranchial placode', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(180037, 'HP:0011410', 'Caesarian section', 'XPO:0100707', 'abnormal central vegetal yolk mass', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(180038, 'HP:0011410', 'Caesarian section', 'XPO:0100665', 'abnormal egg jelly', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(180039, 'HP:0011410', 'Caesarian section', 'XPO:0100786', 'abnormal presumptive axial mesoderm', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(180040, 'HP:0011410', 'Caesarian section', 'XPO:0100344', 'abnormal portion of organism substance', 0.5294117647058824, 1.706362323152461, 0.9504568842024205, 'UPHENO:0002536', 'abnormal anatomical entity'),
(180041, 'HP:0011410', 'Caesarian section', 'XPO:0100225', 'abnormal endocrine system', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(180042, 'HP:0011410', 'Caesarian section', 'XPO:0100289', 'abnormal chondroblast', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(180043, 'HP:0011410', 'Caesarian section', 'XPO:0100956', 'abnormal centrosome', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(180044, 'HP:0011410', 'Caesarian section', 'XPO:0107262', 'abnormal left-right axis', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(180045, 'HP:0011410', 'Caesarian section', 'XPO:0100427', 'abnormal olfactory system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(180046, 'HP:0011410', 'Caesarian section', 'XPO:0100293', 'abnormal duct', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(180047, 'HP:0011410', 'Caesarian section', 'XPO:0100239', 'abnormal acellular anatomical structure', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(180048, 'HP:0011410', 'Caesarian section', 'XPO:0100403', 'abnormal forelimb', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(180049, 'HP:0011410', 'Caesarian section', 'XPO:0100062', 'abnormal anatomical space', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(180050, 'HP:0011410', 'Caesarian section', 'XPO:0102113', 'abnormal anatomical line morphology', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(180051, 'HP:0011410', 'Caesarian section', 'XPO:0101136', 'abnormal ooplasm', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(180052, 'HP:0011410', 'Caesarian section', 'XPO:0100120', 'abnormal genital system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(180053, 'HP:0011410', 'Caesarian section', 'XPO:0101577', 'abnormal notochordal epithelium', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(180054, 'HP:0011410', 'Caesarian section', 'XPO:0100251', 'abnormal proteinaceous extracellular matrix', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(180055, 'HP:0011410', 'Caesarian section', 'XPO:0141748', 'abnormal gas homeostasis', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(180056, 'HP:0011410', 'Caesarian section', 'XPO:0115508', 'abnormally peramorphic growth of whole organism', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(180057, 'HP:0011410', 'Caesarian section', 'XPO:0141714', 'abnormal anterior notochord', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(180058, 'HP:0011410', 'Caesarian section', 'XPO:0101713', 'abnormal anatomical entity in vitro morphology', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(180059, 'HP:0011410', 'Caesarian section', 'XPO:0101141', 'abnormal Keller explant', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(180060, 'HP:0011410', 'Caesarian section', 'XPO:0107263', 'abnormal anatomical side', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(180061, 'HP:0011410', 'Caesarian section', 'XPO:0101228', 'abnormal mesenchymal stem cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(180062, 'HP:0011410', 'Caesarian section', 'XPO:0101497', 'abnormal ciliary axoneme', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(180063, 'HP:0011410', 'Caesarian section', 'XPO:0100688', 'abnormal adipose tissue', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(180064, 'HP:0011410', 'Caesarian section', 'XPO:0142052', 'abnormal nasal region', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(180065, 'HP:0011410', 'Caesarian section', 'XPO:0101224', 'abnormal dorsal involuting marginal zone', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(180066, 'HP:0011410', 'Caesarian section', 'XPO:0101976', 'abnormal portion of organism substance morphology', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(180067, 'HP:0011410', 'Caesarian section', 'XPO:0100135', 'abnormal surface structure', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(180068, 'HP:0011410', 'Caesarian section', 'XPO:0100201', 'abnormal cavitated compound organ', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(180069, 'HP:0011410', 'Caesarian section', 'XPO:0101389', 'abnormal wedge region', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(180070, 'HP:0011410', 'Caesarian section', 'XPO:0101109', 'abnormal egg cell-free extract', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(180071, 'HP:0011410', 'Caesarian section', 'XPO:0100162', 'abnormal presumptive rhombomere', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(180072, 'HP:0011410', 'Caesarian section', 'XPO:0100258', 'abnormal organ part', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(180073, 'HP:0011410', 'Caesarian section', 'XPO:0100715', 'abnormal ciliated cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(180074, 'HP:0011410', 'Caesarian section', 'XPO:0100133', 'abnormal solid compound organ', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(180075, 'HP:0011410', 'Caesarian section', 'XPO:0100721', 'abnormal centromere', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(180076, 'HP:0011410', 'Caesarian section', 'XPO:0100004', 'abnormal cell', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(180077, 'HP:0011410', 'Caesarian section', 'XPO:0101107', 'abnormal erythroid cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(180078, 'HP:0011410', 'Caesarian section', 'XPO:0141738', 'abnormal carbon dioxide homeostasis', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(180079, 'HP:0011410', 'Caesarian section', 'XPO:0101503', 'abnormal organ cortex', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(180080, 'HP:0011410', 'Caesarian section', 'XPO:0141276', 'decreased surface breathing', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(180081, 'HP:0011410', 'Caesarian section', 'XPO:0100796', 'abnormal pseudoblastema', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(180082, 'HP:0011410', 'Caesarian section', 'XPO:0100991', 'abnormal iliac process primordium', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(180083, 'HP:0011410', 'Caesarian section', 'XPO:0115512', 'abnormally semi-erect whole organism', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(180084, 'HP:0011410', 'Caesarian section', 'XPO:0141776', 'abnormal metabolic process', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(180085, 'HP:0011410', 'Caesarian section', 'XPO:0100503', 'abnormal blastomere D2', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(180086, 'HP:0011410', 'Caesarian section', 'XPO:0100032', 'abnormal nervous system', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(180087, 'HP:0011410', 'Caesarian section', 'XPO:0100823', 'abnormal blood', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(180088, 'HP:0011410', 'Caesarian section', 'XPO:0141781', 'abnormal secondary metabolic process', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(180089, 'HP:0011410', 'Caesarian section', 'XPO:0100158', 'abnormal neuromere', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(180090, 'HP:0011410', 'Caesarian section', 'XPO:0100585', 'abnormal elastica externa', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(180091, 'HP:0011410', 'Caesarian section', 'XPO:0101461', 'abnormal sperm entry point', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(180092, 'HP:0011410', 'Caesarian section', 'XPO:0100308', 'abnormal early embryonic cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(180093, 'HP:0011410', 'Caesarian section', 'XPO:0141775', 'abnormal nitrogen compound metabolic process', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(180094, 'HP:0011410', 'Caesarian section', 'XPO:0100581', 'abnormal immune system', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(180095, 'HP:0011410', 'Caesarian section', 'XPO:0101547', 'abnormal lampbrush chromosome', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(180096, 'HP:0011410', 'Caesarian section', 'XPO:0100626', 'abnormal primordial germ cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(180097, 'HP:0011410', 'Caesarian section', 'XPO:0100317', 'abnormal respiratory system', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
