(53608, 'HP:0034686', 'Reduced hepatic urocanase activity', 'XPO:0141266', 'abnormal surface breathing', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(53609, 'HP:0034686', 'Reduced hepatic urocanase activity', 'XPO:0116434', 'abnormal biological process', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(53610, 'HP:0034686', 'Reduced hepatic urocanase activity', 'XPO:0141600', 'absent metamorphosis', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(53611, 'HP:0034686', 'Reduced hepatic urocanase activity', 'XPO:0141881', 'abnormal fructose metabolic process', 0.4230769230769231, 4.758907843651163, 1.418937661667548, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(53612, 'HP:0034686', 'Reduced hepatic urocanase activity', 'XPO:0100546', 'abnormal whole organism', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(53613, 'HP:0034686', 'Reduced hepatic urocanase activity', 'XPO:0100307', 'abnormal blastomere', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(53614, 'HP:0034686', 'Reduced hepatic urocanase activity', 'XPO:0100599', 'abnormal adult immune system', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(53615, 'HP:0034686', 'Reduced hepatic urocanase activity', 'XPO:0101409', 'abnormal perivitelline space', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(53616, 'HP:0034686', 'Reduced hepatic urocanase activity', 'XPO:0101220', 'abnormal centriole', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(53617, 'HP:0034686', 'Reduced hepatic urocanase activity', 'XPO:0141883', 'abnormal glycerol metabolic process', 0.4230769230769231, 4.758907843651163, 1.418937661667548, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(53618, 'HP:0034686', 'Reduced hepatic urocanase activity', 'XPO:0101461', 'abnormal sperm entry point', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(53619, 'HP:0034686', 'Reduced hepatic urocanase activity', 'XPO:0115512', 'abnormally semi-erect whole organism', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(53620, 'HP:0034686', 'Reduced hepatic urocanase activity', 'XPO:0141910', 'abnormal D-ribose metabolic process', 0.4230769230769231, 4.758907843651163, 1.418937661667548, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(53621, 'HP:0034686', 'Reduced hepatic urocanase activity', 'XPO:0100907', 'abnormal cytoplasm', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(53622, 'HP:0034686', 'Reduced hepatic urocanase activity', 'XPO:0141789', 'abnormal hormone catabolic process', 0.44, 4.758907843651163, 1.447038165082909, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(53623, 'HP:0034686', 'Reduced hepatic urocanase activity', 'XPO:0101326', 'abnormal cementoblast', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(53624, 'HP:0034686', 'Reduced hepatic urocanase activity', 'XPO:0141276', 'decreased surface breathing', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(53625, 'HP:0034686', 'Reduced hepatic urocanase activity', 'XPO:0100724', 'abnormal kinetochore', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(53626, 'HP:0034686', 'Reduced hepatic urocanase activity', 'XPO:0100533', 'abnormal melanoblast', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(53627, 'HP:0034686', 'Reduced hepatic urocanase activity', 'XPO:0101297', 'abnormal barrier cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(53628, 'HP:0034686', 'Reduced hepatic urocanase activity', 'XPO:0141771', 'abnormal urea homeostasis', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(53629, 'HP:0034686', 'Reduced hepatic urocanase activity', 'XPO:0141784', 'abnormal cellular hormone metabolic process', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(53630, 'HP:0034686', 'Reduced hepatic urocanase activity', 'XPO:0141877', 'abnormal 2-deoxyribose 1-phosphate metabolic process', 0.4583333333333333, 4.758907843651163, 1.4768771428276568, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(53631, 'HP:0034686', 'Reduced hepatic urocanase activity', 'XPO:0141898', 'abnormal maltose metabolic process', 0.4583333333333333, 4.758907843651163, 1.4768771428276568, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(53632, 'HP:0034686', 'Reduced hepatic urocanase activity', 'XPO:0141264', 'abnormal schooling behavior', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(53633, 'HP:0034686', 'Reduced hepatic urocanase activity', 'XPO:0141854', 'abnormal glutathione metabolic process', 0.4230769230769231, 4.758907843651163, 1.418937661667548, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(53634, 'HP:0034686', 'Reduced hepatic urocanase activity', 'XPO:0100585', 'abnormal elastica externa', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(53635, 'HP:0034686', 'Reduced hepatic urocanase activity', 'XPO:0100232', 'abnormal lymphatic system', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(53636, 'HP:0034686', 'Reduced hepatic urocanase activity', 'XPO:0100477', 'abnormal pericyte', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(53637, 'HP:0034686', 'Reduced hepatic urocanase activity', 'XPO:0107259', 'abnormal animal-vegetal axis', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(53638, 'HP:0034686', 'Reduced hepatic urocanase activity', 'XPO:0141271', 'increased surface breathing', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(53639, 'HP:0034686', 'Reduced hepatic urocanase activity', 'XPO:0101498', 'abnormal stage II oocyte', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(53640, 'HP:0034686', 'Reduced hepatic urocanase activity', 'XPO:0101467', 'abnormal alkali secreting cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(53641, 'HP:0034686', 'Reduced hepatic urocanase activity', 'XPO:0100258', 'abnormal organ part', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(53642, 'HP:0034686', 'Reduced hepatic urocanase 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'),
(53643, 'HP:0034686', 'Reduced hepatic urocanase activity', 'XPO:0133403', 'abnormal developmental process', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(53644, 'HP:0034686', 'Reduced hepatic urocanase activity', 'XPO:0100006', 'abnormal anatomical structure', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(53645, 'HP:0034686', 'Reduced hepatic urocanase activity', 'XPO:0100285', 'abnormal progenitor cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(53646, 'HP:0034686', 'Reduced hepatic urocanase activity', 'XPO:0100372', 'abnormal hematological system', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(53647, 'HP:0034686', 'Reduced hepatic urocanase activity', 'XPO:0101448', 'abnormal myelin accumulating cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(53648, 'HP:0034686', 'Reduced hepatic urocanase activity', 'XPO:0101132', 'abnormal apoptotic cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(53649, 'HP:0034686', 'Reduced hepatic urocanase activity', 'XPO:0100239', 'abnormal acellular anatomical structure', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(53650, 'HP:0034686', 'Reduced hepatic urocanase activity', 'XPO:0107312', 'abnormal filopodium', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(53651, 'HP:0034686', 'Reduced hepatic urocanase activity', 'XPO:0141778', 'abnormal biosynthetic process', 0.5238095238095238, 4.758907843651163, 1.5788480773767701, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(53652, 'HP:0034686', 'Reduced hepatic urocanase activity', 'XPO:0101569', 'abnormal activin-induced ectoderm', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(53653, 'HP:0034686', 'Reduced hepatic urocanase activity', 'XPO:0101366', 'abnormal morula cell', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(53654, 'HP:0034686', 'Reduced hepatic urocanase activity', 'XPO:0141754', 'abnormal homeostatic process', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(53655, 'HP:0034686', 'Reduced hepatic urocanase activity', 'XPO:0115509', 'abnormally semi-viable whole organism', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(53656, 'HP:0034686', 'Reduced hepatic urocanase activity', 'XPO:0101513', 'abnormal basal body', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(53657, 'HP:0034686', 'Reduced hepatic urocanase activity', 'XPO:0141795', 'abnormal glycosylation', 0.4782608695652174, 4.758907843651163, 1.508641575552437, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(53658, 'HP:0034686', 'Reduced hepatic urocanase activity', 'XPO:0141904', 'abnormal glucosamine metabolic process', 0.5238095238095238, 4.758907843651163, 1.5788480773767701, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(53659, 'HP:0034686', 'Reduced hepatic urocanase activity', 'XPO:0131723', 'abnormal pathway-restricted SMAD protein phosphorylation', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(53660, 'HP:0034686', 'Reduced hepatic urocanase activity', 'XPO:0141315', 'abnormal anatomical region', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(53661, 'HP:0034686', 'Reduced hepatic urocanase activity', 'XPO:0141892', 'abnormal inositol metabolic process', 0.4782608695652174, 4.758907843651163, 1.508641575552437, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(53662, 'HP:0034686', 'Reduced hepatic urocanase activity', 'XPO:0100084', 'abnormal anatomical group', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(53663, 'HP:0005905', 'Abnormal cervical curvature', 'XPO:0100584', 'abnormal vertebral column', 0.46296296296296297, 8.05344015541032, 1.9309180501496346, 'UPHENO:0002813', 'abnormal vertebral column'),
(53664, 'HP:0005905', 'Abnormal cervical curvature', 'XPO:0100968', 'abnormal cervical vertebra', 0.4246575342465753, 11.7857850889227, 2.237168396661719, 'HP:0003319', 'Abnormality of the cervical spine'),
(53665, 'HP:0005905', 'Abnormal cervical curvature', 'XPO:0100693', 'abnormal vertebral centrum', 0.4098360655737705, 8.05344015541032, 1.816752660002781, 'UPHENO:0002813', 'abnormal vertebral column'),
(53666, 'HP:0005905', 'Abnormal cervical curvature', 'XPO:0102216', 'abnormal vertebral column morphology', 0.4406779661016949, 8.361863005979023, 1.9196064133816184, 'UPHENO:0076695', 'abnormal vertebral column morphology'),
(53667, 'HP:0005905', 'Abnormal cervical curvature', 'XPO:0102600', 'abnormal cervical vertebra morphology', 0.43333333333333335, 12.167655724266345, 2.296225340389908, 'UPHENO:0081579', 'abnormal cervical vertebra morphology'),
(53668, 'HP:0005905', 'Abnormal cervical curvature', 'XPO:0100226', 'abnormal vertebral element', 0.4166666666666667, 8.05344015541032, 1.8318297040812228, 'UPHENO:0002813', 'abnormal vertebral column'),
(53669, 'HP:0034131', 'Anti-GT1b antibody positivity', 'XPO:0100449', 'abnormal lymphocyte', 0.40625, 5.64885357140806, 1.5148751642906173, 'HP:0002715', 'Abnormality of the immune system'),
(53670, 'HP:0034131', 'Anti-GT1b antibody positivity', 'XPO:0100745', 'abnormal anterior lymph sac', 0.41935483870967744, 5.64885357140806, 1.5391147060347428, 'HP:0002715', 'Abnormality of the immune system'),
(53671, 'HP:0034131', 'Anti-GT1b antibody positivity', 'XPO:0100232', 'abnormal lymphatic system', 0.4642857142857143, 5.64885357140806, 1.6194696710023933, 'HP:0002715', 'Abnormality of the immune system'),
(53672, 'HP:0034131', 'Anti-GT1b antibody positivity', 'XPO:0101451', 'abnormal dorsal lymph space', 0.43333333333333335, 5.64885357140806, 1.5645563421015427, 'HP:0002715', 'Abnormality of the immune system'),
(53673, 'HP:0034131', 'Anti-GT1b antibody positivity', 'XPO:0141497', 'abnormal lymphoblast', 0.40625, 5.64885357140806, 1.5148751642906173, 'HP:0002715', 'Abnormality of the immune system'),
(53674, 'HP:0034131', 'Anti-GT1b antibody positivity', 'XPO:0100599', 'abnormal adult immune system', 0.4482758620689655, 5.64885357140806, 1.5913028324062968, 'HP:0002715', 'Abnormality of the immune system'),
(53675, 'HP:0034131', 'Anti-GT1b antibody positivity', 'XPO:0101221', 'abnormal larval immune system', 0.4482758620689655, 5.64885357140806, 1.5913028324062968, 'HP:0002715', 'Abnormality of the immune system'),
(53676, 'HP:0034131', 'Anti-GT1b antibody positivity', 'XPO:0101029', 'abnormal right spleen primordium', 0.40625, 5.64885357140806, 1.5148751642906173, 'HP:0002715', 'Abnormality of the immune system'),
(53677, 'HP:0034131', 'Anti-GT1b antibody positivity', 'XPO:0100581', 'abnormal immune system', 0.4642857142857143, 5.64885357140806, 1.6194696710023933, 'HP:0002715', 'Abnormality of the immune system'),
(53678, 'HP:0012248', 'Prolonged PR interval', 'XPO:0100054', 'abnormal blood vessel', 0.4117647058823529, 5.249153838287537, 1.4701755971154233, 'UPHENO:0080362', 'abnormal cardiovascular system'),
(53679, 'HP:0030502', 'Retinoschisis', 'XPO:0130048', 'increased size of the optic disc', 0.43661971830985913, 6.575878401988876, 1.6944492248268372, 'UPHENO:0087924', 'abnormal camera-type eye morphology'),
(53680, 'HP:0030502', 'Retinoschisis', 'XPO:0141138', 'abnormally necrotic retinal inner plexiform layer', 0.48314606741573035, 8.040873045973026, 1.9710190741722953, 'HP:0000479', 'Abnormal retinal morphology'),
(53681, 'HP:0030502', 'Retinoschisis', 'XPO:0103780', 'decreased size of the bipolar neuron in the retinal inner plexiform layer', 0.4056603773584906, 8.040873045973026, 1.8060630094548564, 'HP:0000479', 'Abnormal retinal morphology'),
(53682, 'HP:0030502', 'Retinoschisis', 'XPO:0140948', 'abnormally necrotic retinal inner nuclear layer', 0.48314606741573035, 8.040873045973026, 1.9710190741722953, 'HP:0000479', 'Abnormal retinal morphology'),
(53683, 'HP:0030502', 'Retinoschisis', 'XPO:0128261', 'decreased size of the optic fiber layer', 0.4777777777777778, 8.040873045973026, 1.960038381077836, 'HP:0000479', 'Abnormal retinal morphology'),
(53684, 'HP:0030502', 'Retinoschisis', 'XPO:0102815', 'abnormal retinal ganglion cell morphology', 0.48863636363636365, 8.040873045973026, 1.982186410418029, 'HP:0000479', 'Abnormal retinal morphology'),
(53685, 'HP:0030502', 'Retinoschisis', 'XPO:0128300', 'decreased size of the retina', 0.5733333333333334, 8.040873045973026, 2.147114469784475, 'HP:0000479', 'Abnormal retinal morphology'),
(53686, 'HP:0030502', 'Retinoschisis', 'XPO:0129971', 'increased size of the retinal ganglion cell', 0.42574257425742573, 8.040873045973026, 1.850227550835222, 'HP:0000479', 'Abnormal retinal morphology'),
(53687, 'HP:0030502', 'Retinoschisis', 'XPO:0129810', 'increased size of the retinal progenitor cell region', 0.5584415584415584, 8.040873045973026, 2.1190464070010115, 'HP:0000479', 'Abnormal retinal morphology'),
(53688, 'HP:0030502', 'Retinoschisis', 'XPO:0102226', 'abnormal Jacobsons organ morphology', 0.4375, 5.788671267106304, 1.5913967699348293, 'UPHENO:0087472', 'abnormal face morphology'),
(53689, 'HP:0030502', 'Retinoschisis', 'XPO:0141323', 'edematous eye', 0.49295774647887325, 6.887869297006056, 1.8426688597502066, 'HP:0012372', 'Abnormal eye morphology'),
(53690, 'HP:0030502', 'Retinoschisis', 'XPO:0128646', 'decreased size of the outer limiting membrane', 0.4777777777777778, 8.040873045973026, 1.960038381077836, 'HP:0000479', 'Abnormal retinal morphology'),
(53691, 'HP:0030502', 'Retinoschisis', 'XPO:0103142', 'abnormal optic nerve morphology', 0.43157894736842106, 7.796308075334707, 1.8343179747559781, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(53692, 'HP:0030502', 'Retinoschisis', 'XPO:0140869', 'abnormally necrotic optic chiasm', 0.47674418604651164, 7.796308075334707, 1.9279119657140185, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(53693, 'HP:0030502', 'Retinoschisis', 'XPO:0102939', 'abnormal retinal ganglion cell layer morphology', 0.524390243902439, 8.040873045973026, 2.053425279323877, 'HP:0000479', 'Abnormal retinal morphology'),
(53694, 'HP:0030502', 'Retinoschisis', 'XPO:0140317', 'abnormally necrotic retinal progenitor cell', 0.5, 8.040873045973026, 2.0051026215599324, 'HP:0000479', 'Abnormal retinal morphology'),
(53695, 'HP:0030502', 'Retinoschisis', 'XPO:0140271', 'abnormally necrotic peripheral retina', 0.5584415584415584, 8.040873045973026, 2.1190464070010115, 'HP:0000479', 'Abnormal retinal morphology'),
(53696, 'HP:0030502', 'Retinoschisis', 'XPO:0100371', 'abnormal hyaloid blood vessel', 0.47692307692307695, 6.887869297006056, 1.8124524320853552, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(53697, 'HP:0030502', 'Retinoschisis', 'XPO:0128100', 'decreased size of the inner limiting membrane', 0.4777777777777778, 8.040873045973026, 1.960038381077836, 'HP:0000479', 'Abnormal retinal morphology'),
(53698, 'HP:0030502', 'Retinoschisis', 'XPO:0101861', 'abnormal photoreceptor layer morphology', 0.5308641975308642, 8.040873045973026, 2.066061861851679, 'HP:0000479', 'Abnormal retinal morphology'),
(53699, 'HP:0030502', 'Retinoschisis', 'XPO:0102805', 'abnormal retinal layer morphology', 0.6515151515151515, 8.040873045973026, 2.288831715277734, 'HP:0000479', 'Abnormal retinal morphology'),
(53700, 'HP:0030502', 'Retinoschisis', 'XPO:0129038', 'decreased size of the retinal outer nuclear layer', 0.4777777777777778, 8.040873045973026, 1.960038381077836, 'HP:0000479', 'Abnormal retinal morphology'),
(53701, 'HP:0030502', 'Retinoschisis', 'XPO:0140218', 'abnormally necrotic sclera', 0.4666666666666667, 6.887869297006056, 1.7928577760852904, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(53702, 'HP:0030502', 'Retinoschisis', 'XPO:0129680', 'increased size of the retinal rod cell', 0.43, 8.040873045973026, 1.859455675666511, 'HP:0000479', 'Abnormal retinal morphology'),
(53703, 'HP:0030502', 'Retinoschisis', 'XPO:0102505', 'abnormal retinal stem cell region morphology', 0.5972222222222222, 8.040873045973026, 2.191389529299339, 'HP:0000479', 'Abnormal retinal morphology'),
(53704, 'HP:0030502', 'Retinoschisis', 'XPO:0133354', 'fused eyes', 0.4861111111111111, 6.887869297006056, 1.8298278053291577, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(53705, 'HP:0030502', 'Retinoschisis', 'XPO:0128875', 'decreased size of the photoreceptor layer', 0.48314606741573035, 8.040873045973026, 1.9710190741722953, 'HP:0000479', 'Abnormal retinal morphology'),
(53706, 'HP:0030502', 'Retinoschisis', 'XPO:0129419', 'decreased size of the pupil', 0.4117647058823529, 6.887869297006056, 1.6840966347682629, 'HP:0012372', 'Abnormal eye morphology'),
(53707, 'HP:0030502', 'Retinoschisis', 'XPO:0140081', 'abnormally necrotic amacrine cell', 0.45263157894736844, 8.040873045973026, 1.9077612698957138, 'HP:0000479', 'Abnormal retinal morphology'),
(53708, 'HP:0030502', 'Retinoschisis', 'XPO:0139912', 'abnormally necrotic optic fiber layer', 0.48314606741573035, 8.040873045973026, 1.9710190741722953, 'HP:0000479', 'Abnormal retinal morphology'),
(53709, 'HP:0030502', 'Retinoschisis', 'XPO:0128669', 'decreased size of the ciliary marginal zone', 0.5, 8.040873045973026, 2.0051026215599324, 'HP:0000479', 'Abnormal retinal morphology'),
(53710, 'HP:0030502', 'Retinoschisis', 'XPO:0115417', 'abnormally wholly ventralized eye', 0.4605263157894737, 6.887869297006056, 1.7810236020304815, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(53711, 'HP:0030502', 'Retinoschisis', 'XPO:0103155', 'abnormal bipolar neuron morphology', 0.48314606741573035, 8.040873045973026, 1.9710190741722953, 'HP:0000479', 'Abnormal retinal morphology'),
(53712, 'HP:0030502', 'Retinoschisis', 'XPO:0128295', 'decreased size of the retinal neural layer', 0.4777777777777778, 8.040873045973026, 1.960038381077836, 'HP:0000479', 'Abnormal retinal morphology'),
(53713, 'HP:0030502', 'Retinoschisis', 'XPO:0103186', 'abnormal peripheral retina morphology', 0.6056338028169014, 8.040873045973026, 2.206767890105474, 'HP:0000479', 'Abnormal retinal morphology'),
(53714, 'HP:0030502', 'Retinoschisis', 'XPO:0103210', 'abnormal pupil morphology', 0.4430379746835443, 6.887869297006056, 1.7468794071802813, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(53715, 'HP:0030502', 'Retinoschisis', 'XPO:0103226', 'abnormal retinal outer plexiform layer morphology', 0.524390243902439, 8.040873045973026, 2.053425279323877, 'HP:0000479', 'Abnormal retinal morphology'),
(53716, 'HP:0030502', 'Retinoschisis', 'XPO:0130515', 'increased size of the retinal outer nuclear layer', 0.4777777777777778, 8.040873045973026, 1.960038381077836, 'HP:0000479', 'Abnormal retinal morphology'),
(53717, 'HP:0030502', 'Retinoschisis', 'XPO:0130413', 'increased size of the central retina', 0.589041095890411, 8.040873045973026, 2.1763282544036455, 'HP:0000479', 'Abnormal retinal morphology'),
(53718, 'HP:0030502', 'Retinoschisis', 'XPO:0129741', 'increased size of the optic fiber layer', 0.4777777777777778, 8.040873045973026, 1.960038381077836, 'HP:0000479', 'Abnormal retinal morphology'),
(53719, 'HP:0030502', 'Retinoschisis', 'XPO:0103926', 'decreased pigmentation in the retinal pigmented epithelium', 0.5058823529411764, 8.040873045973026, 2.0168628550791743, 'HP:0000479', 'Abnormal retinal morphology'),
(53720, 'HP:0030502', 'Retinoschisis', 'XPO:0130257', 'increased size of the retinal blood vessel', 0.4574468085106383, 8.040873045973026, 1.9178820903589395, 'HP:0000479', 'Abnormal retinal morphology'),
(53721, 'HP:0030502', 'Retinoschisis', 'XPO:0128884', 'decreased size of the retinal pigmented epithelium', 0.4725274725274725, 8.040873045973026, 1.9492391893577128, 'HP:0000479', 'Abnormal retinal morphology'),
(53722, 'HP:0030502', 'Retinoschisis', 'XPO:0127907', 'abnormally localised optic choroid vascular plexus', 0.4025974025974026, 6.887869297006056, 1.6652442128423794, 'HP:0012372', 'Abnormal eye morphology'),
(53723, 'HP:0030502', 'Retinoschisis', 'XPO:0129580', 'increased size of the inner limiting membrane', 0.4777777777777778, 8.040873045973026, 1.960038381077836, 'HP:0000479', 'Abnormal retinal morphology'),
(53724, 'HP:0030502', 'Retinoschisis', 'XPO:0140391', 'abnormally necrotic central retina', 0.6056338028169014, 8.040873045973026, 2.206767890105474, 'HP:0000479', 'Abnormal retinal morphology'),
(53725, 'HP:0030502', 'Retinoschisis', 'XPO:0139731', 'abnormally necrotic eye', 0.4605263157894737, 6.887869297006056, 1.7810236020304815, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(53726, 'HP:0030502', 'Retinoschisis', 'XPO:0103706', 'increased pigmentation in the optic nerve', 0.41836734693877553, 7.796308075334707, 1.8060234564908433, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(53727, 'HP:0030502', 'Retinoschisis', 'XPO:0130001', 'increased size of the horizontal cell', 0.43434343434343436, 8.040873045973026, 1.8688232698432123, 'HP:0000479', 'Abnormal retinal morphology'),
(53728, 'HP:0030502', 'Retinoschisis', 'XPO:0140473', 'abnormally necrotic lens transitional zone', 0.4375, 6.887869297006056, 1.7359270772241988, 'HP:0012372', 'Abnormal eye morphology'),
(53729, 'HP:0030502', 'Retinoschisis', 'XPO:0140671', 'abnormally necrotic retinal ganglion cell', 0.46236559139784944, 8.040873045973026, 1.9281657141584967, 'HP:0000479', 'Abnormal retinal morphology'),
(53730, 'HP:0030502', 'Retinoschisis', 'XPO:0133369', 'eye fused with brain', 0.4861111111111111, 6.887869297006056, 1.8298278053291577, 'HP:0012372', 'Abnormal eye morphology'),
(53731, 'HP:0030502', 'Retinoschisis', 'XPO:0141638', 'neoplastic eye', 0.4861111111111111, 6.887869297006056, 1.8298278053291577, 'HP:0012372', 'Abnormal eye morphology'),
(53732, 'HP:0030502', 'Retinoschisis', 'XPO:0127563', 'abnormally localised retinal blood vessel', 0.5584415584415584, 8.040873045973026, 2.1190464070010115, 'HP:0000479', 'Abnormal retinal morphology'),
(53733, 'HP:0030502', 'Retinoschisis', 'XPO:0102963', 'abnormal retinal outer nuclear layer morphology', 0.524390243902439, 8.040873045973026, 2.053425279323877, 'HP:0000479', 'Abnormal retinal morphology'),
(53734, 'HP:0030502', 'Retinoschisis', 'XPO:0103160', 'abnormal choroid morphology', 0.44285714285714284, 6.575878401988876, 1.7065095138559256, 'UPHENO:0087924', 'abnormal camera-type eye morphology'),
(53735, 'HP:0030502', 'Retinoschisis', 'XPO:0128918', 'decreased size of the choroid', 0.4025974025974026, 6.575878401988876, 1.627092979653308, 'UPHENO:0087924', 'abnormal camera-type eye morphology'),
(53736, 'HP:0030502', 'Retinoschisis', 'XPO:0141333', 'increased pigmentation in the retinal pigmented epithelium', 0.5058823529411764, 8.040873045973026, 2.0168628550791743, 'HP:0000479', 'Abnormal retinal morphology'),
(53737, 'HP:0030502', 'Retinoschisis', 'XPO:0141182', 'abnormally necrotic inner limiting membrane', 0.48314606741573035, 8.040873045973026, 1.9710190741722953, 'HP:0000479', 'Abnormal retinal morphology'),
(53738, 'HP:0030502', 'Retinoschisis', 'XPO:0107252', 'decreased size of the globe', 0.41333333333333333, 6.575878401988876, 1.6486448190828538, 'UPHENO:0087924', 'abnormal camera-type eye morphology'),
(53739, 'HP:0030502', 'Retinoschisis', 'XPO:0103110', 'abnormal lens fiber cell mass morphology', 0.4117647058823529, 6.887869297006056, 1.6840966347682629, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(53740, 'HP:0030502', 'Retinoschisis', 'XPO:0129138', 'decreased size of the retinal progenitor cell', 0.4574468085106383, 8.040873045973026, 1.9178820903589395, 'HP:0000479', 'Abnormal retinal morphology'),
(53741, 'HP:0030502', 'Retinoschisis', 'XPO:0130189', 'increased size of the optic chiasm', 0.45555555555555555, 7.796308075334707, 1.884582568247241, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(53742, 'HP:0030502', 'Retinoschisis', 'XPO:0102232', 'abnormal eye photoreceptor cell morphology', 0.5058823529411764, 8.040873045973026, 2.0168628550791743, 'HP:0000479', 'Abnormal retinal morphology'),
(53743, 'HP:0030502', 'Retinoschisis', 'XPO:0102441', 'abnormal retinal inner plexiform layer morphology', 0.524390243902439, 8.040873045973026, 2.053425279323877, 'HP:0000479', 'Abnormal retinal morphology'),
(53744, 'HP:0030502', 'Retinoschisis', 'XPO:0100779', 'abnormal optic choroid vascular plexus', 0.4696969696969697, 6.887869297006056, 1.7986693238259617, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(53745, 'HP:0030502', 'Retinoschisis', 'XPO:0101315', 'abnormal hyaloid vascular plexus', 0.4626865671641791, 6.887869297006056, 1.7851959556606887, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(53746, 'HP:0030502', 'Retinoschisis', 'XPO:0102663', 'abnormal retinal progenitor cell morphology', 0.5308641975308642, 8.040873045973026, 2.066061861851679, 'HP:0000479', 'Abnormal retinal morphology'),
(53747, 'HP:0030502', 'Retinoschisis', 'XPO:0130265', 'increased size of the peripheral retina', 0.5443037974683544, 8.040873045973026, 2.0920510830006163, 'HP:0000479', 'Abnormal retinal morphology'),
(53748, 'HP:0030502', 'Retinoschisis', 'XPO:0102266', 'abnormal horizontal cell morphology', 0.5, 8.040873045973026, 2.0051026215599324, 'HP:0000479', 'Abnormal retinal morphology'),
(53749, 'HP:0030502', 'Retinoschisis', 'XPO:0130353', 'increased size of the photoreceptor layer', 0.48314606741573035, 8.040873045973026, 1.9710190741722953, 'HP:0000479', 'Abnormal retinal morphology'),
(53750, 'HP:0030502', 'Retinoschisis', 'XPO:0130845', 'increased size of the retinal outer plexiform layer', 0.4777777777777778, 8.040873045973026, 1.960038381077836, 'HP:0000479', 'Abnormal retinal morphology'),
(53751, 'HP:0030502', 'Retinoschisis', 'XPO:0130506', 'increased size of the Muller cell', 0.48314606741573035, 8.040873045973026, 1.9710190741722953, 'HP:0000479', 'Abnormal retinal morphology'),
(53752, 'HP:0030502', 'Retinoschisis', 'XPO:0115423', 'abnormally incomplete structure of eye', 0.5, 6.887869297006056, 1.8557841061133777, 'HP:0012372', 'Abnormal eye morphology'),
(53753, 'HP:0030502', 'Retinoschisis', 'XPO:0128779', 'decreased size of the retinal blood vessel', 0.4574468085106383, 8.040873045973026, 1.9178820903589395, 'HP:0000479', 'Abnormal retinal morphology'),
(53754, 'HP:0030502', 'Retinoschisis', 'XPO:0128599', 'decreased size of the olfactory pit', 0.417910447761194, 5.788671267106304, 1.5553604730668558, 'UPHENO:0087472', 'abnormal face morphology'),
(53755, 'HP:0030502', 'Retinoschisis', 'XPO:0103086', 'abnormal amacrine cell morphology', 0.48314606741573035, 8.040873045973026, 1.9710190741722953, 'HP:0000479', 'Abnormal retinal morphology'),
(53756, 'HP:0030502', 'Retinoschisis', 'XPO:0102196', 'abnormal central retina morphology', 0.6323529411764706, 8.040873045973026, 2.2549212226256703, 'HP:0000479', 'Abnormal retinal morphology'),
(53757, 'HP:0030502', 'Retinoschisis', 'XPO:0128848', 'decreased size of the retinal cone cell', 0.43, 8.040873045973026, 1.859455675666511, 'HP:0000479', 'Abnormal retinal morphology'),
(53758, 'HP:0030502', 'Retinoschisis', 'XPO:0129911', 'increased size of the retinal inner nuclear layer', 0.4777777777777778, 8.040873045973026, 1.960038381077836, 'HP:0000479', 'Abnormal retinal morphology'),
(53759, 'HP:0030502', 'Retinoschisis', 'XPO:0140346', 'abnormally necrotic retinal blood vessel', 0.4673913043478261, 8.040873045973026, 1.938616553383523, 'HP:0000479', 'Abnormal retinal morphology'),
(53760, 'HP:0030502', 'Retinoschisis', 'XPO:0129083', 'decreased size of the bipolar neuron', 0.4174757281553398, 8.040873045973026, 1.8321761186829812, 'HP:0000479', 'Abnormal retinal morphology'),
(53761, 'HP:0030502', 'Retinoschisis', 'XPO:0128201', 'decreased size of the eye photoreceptor cell', 0.44329896907216493, 8.040873045973026, 1.8879911895239345, 'HP:0000479', 'Abnormal retinal morphology'),
(53762, 'HP:0030502', 'Retinoschisis', 'XPO:0102966', 'abnormal olfactory pit morphology', 0.45161290322580644, 5.788671267106304, 1.6168607351153301, 'UPHENO:0087472', 'abnormal face morphology'),
(53763, 'HP:0030502', 'Retinoschisis', 'XPO:0125589', 'absent hyaloid blood vessel', 0.4025974025974026, 6.887869297006056, 1.6652442128423794, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(53764, 'HP:0030502', 'Retinoschisis', 'XPO:0130761', 'increased size of the retinal inner plexiform layer', 0.4777777777777778, 8.040873045973026, 1.960038381077836, 'HP:0000479', 'Abnormal retinal morphology'),
(53765, 'HP:0030502', 'Retinoschisis', 'XPO:0128807', 'decreased size of the lens transitional zone', 0.4268292682926829, 6.887869297006056, 1.714626551799759, 'HP:0012372', 'Abnormal eye morphology'),
(53766, 'HP:0030502', 'Retinoschisis', 'XPO:0130122', 'increased size of the retinal layer', 0.589041095890411, 8.040873045973026, 2.1763282544036455, 'HP:0000479', 'Abnormal retinal morphology'),
(53767, 'HP:0030502', 'Retinoschisis', 'XPO:0130148', 'increased size of the ciliary marginal zone', 0.5, 8.040873045973026, 2.0051026215599324, 'HP:0000479', 'Abnormal retinal morphology'),
(53768, 'HP:0030502', 'Retinoschisis', 'XPO:0102581', 'abnormal outer limiting membrane morphology', 0.524390243902439, 8.040873045973026, 2.053425279323877, 'HP:0000479', 'Abnormal retinal morphology'),
(53769, 'HP:0030502', 'Retinoschisis', 'XPO:0129532', 'increased size of the iris', 0.4069767441860465, 6.887869297006056, 1.6742767456052652, 'HP:0012372', 'Abnormal eye morphology'),
(53770, 'HP:0030502', 'Retinoschisis', 'XPO:0129371', 'decreased size of the retinal outer plexiform layer', 0.4777777777777778, 8.040873045973026, 1.960038381077836, 'HP:0000479', 'Abnormal retinal morphology'),
(53771, 'HP:0030502', 'Retinoschisis', 'XPO:0139887', 'abnormally necrotic Muller cell', 0.5308641975308642, 8.040873045973026, 2.066061861851679, 'HP:0000479', 'Abnormal retinal morphology'),
(53772, 'HP:0030502', 'Retinoschisis', 'XPO:0102851', 'abnormal retinal rod cell morphology', 0.4942528735632184, 8.040873045973026, 1.9935457378573478, 'HP:0000479', 'Abnormal retinal morphology'),
(53773, 'HP:0030502', 'Retinoschisis', 'XPO:0128787', 'decreased size of the peripheral retina', 0.5443037974683544, 8.040873045973026, 2.0920510830006163, 'HP:0000479', 'Abnormal retinal morphology'),
(53774, 'HP:0030502', 'Retinoschisis', 'XPO:0129062', 'decreased size of the ciliary body', 0.4117647058823529, 6.887869297006056, 1.6840966347682629, 'HP:0012372', 'Abnormal eye morphology'),
(53775, 'HP:0030502', 'Retinoschisis', 'XPO:0101359', 'abnormal hyaloid artery', 0.45454545454545453, 6.887869297006056, 1.769420718895678, 'HP:0012372', 'Abnormal eye morphology'),
(53776, 'HP:0030502', 'Retinoschisis', 'XPO:0128710', 'decreased size of the optic chiasm', 0.45555555555555555, 7.796308075334707, 1.884582568247241, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(53777, 'HP:0030502', 'Retinoschisis', 'XPO:0102239', 'abnormal retinal pigmented epithelium morphology', 0.524390243902439, 8.040873045973026, 2.053425279323877, 'HP:0000479', 'Abnormal retinal morphology'),
(53778, 'HP:0030502', 'Retinoschisis', 'XPO:0102818', 'abnormal optic chiasm morphology', 0.5061728395061729, 7.796308075334707, 1.9865244514370002, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(53779, 'HP:0030502', 'Retinoschisis', 'XPO:0102017', 'abnormal retinal neural layer morphology', 0.5308641975308642, 8.040873045973026, 2.066061861851679, 'HP:0000479', 'Abnormal retinal morphology'),
(53780, 'HP:0030502', 'Retinoschisis', 'XPO:0103184', 'abnormal inner limiting membrane morphology', 0.524390243902439, 8.040873045973026, 2.053425279323877, 'HP:0000479', 'Abnormal retinal morphology'),
(53781, 'HP:0030502', 'Retinoschisis', 'XPO:0128935', 'decreased size of the central retina', 0.589041095890411, 8.040873045973026, 2.1763282544036455, 'HP:0000479', 'Abnormal retinal morphology'),
(53782, 'HP:0030502', 'Retinoschisis', 'XPO:0102513', 'abnormal sclera morphology', 0.5, 6.887869297006056, 1.8557841061133777, 'HP:0012372', 'Abnormal eye morphology'),
(53783, 'HP:0030502', 'Retinoschisis', 'XPO:0102411', 'abnormal optic choroid vascular plexus morphology', 0.42045454545454547, 7.796308075334707, 1.8105228990649238, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(53784, 'HP:0030502', 'Retinoschisis', 'XPO:0103022', 'abnormal ciliary body morphology', 0.45454545454545453, 6.887869297006056, 1.769420718895678, 'HP:0012372', 'Abnormal eye morphology'),
(53785, 'HP:0030502', 'Retinoschisis', 'XPO:0141033', 'abnormally necrotic photoreceptor layer', 0.48863636363636365, 8.040873045973026, 1.982186410418029, 'HP:0000479', 'Abnormal retinal morphology'),
(53786, 'HP:0030502', 'Retinoschisis', 'XPO:0103376', 'increased size of the eye', 0.4375, 6.887869297006056, 1.7359270772241988, 'HP:0012372', 'Abnormal eye morphology'),
(53787, 'HP:0030502', 'Retinoschisis', 'XPO:0103336', 'decreased size of the eye', 0.4375, 6.887869297006056, 1.7359270772241988, 'HP:0012372', 'Abnormal eye morphology'),
(53788, 'HP:0030502', 'Retinoschisis', 'XPO:0140593', 'abnormally necrotic Jacobsons organ', 0.4057971014492754, 5.788671267106304, 1.532653261972336, 'UPHENO:0087472', 'abnormal face morphology'),
(53789, 'HP:0030502', 'Retinoschisis', 'XPO:0140620', 'abnormally necrotic horizontal cell', 0.4725274725274725, 8.040873045973026, 1.9492391893577128, 'HP:0000479', 'Abnormal retinal morphology'),
(53790, 'HP:0030502', 'Retinoschisis', 'XPO:0140375', 'abnormally necrotic lens', 0.44871794871794873, 6.887869297006056, 1.7580416894914344, 'HP:0012372', 'Abnormal eye morphology'),
(53791, 'HP:0030502', 'Retinoschisis', 'XPO:0130285', 'increased size of the lens transitional zone', 0.4268292682926829, 6.887869297006056, 1.714626551799759, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(53792, 'HP:0030502', 'Retinoschisis', 'XPO:0129258', 'decreased size of the amacrine cell', 0.4174757281553398, 8.040873045973026, 1.8321761186829812, 'HP:0000479', 'Abnormal retinal morphology'),
(53793, 'HP:0030502', 'Retinoschisis', 'XPO:0102756', 'abnormal Muller cell morphology', 0.5657894736842105, 8.040873045973026, 2.1329419421640696, 'HP:0000479', 'Abnormal retinal morphology'),
(53794, 'HP:0030502', 'Retinoschisis', 'XPO:0130539', 'increased size of the ciliary body', 0.4117647058823529, 6.887869297006056, 1.6840966347682629, 'HP:0012372', 'Abnormal eye morphology'),
(53795, 'HP:0030502', 'Retinoschisis', 'XPO:0140797', 'abnormally necrotic bipolar neuron', 0.45263157894736844, 8.040873045973026, 1.9077612698957138, 'HP:0000479', 'Abnormal retinal morphology'),
(53796, 'HP:0030502', 'Retinoschisis', 'XPO:0129780', 'increased size of the retina', 0.5733333333333334, 8.040873045973026, 2.147114469784475, 'HP:0000479', 'Abnormal retinal morphology'),
(53797, 'HP:0030502', 'Retinoschisis', 'XPO:0130859', 'increased size of the globe', 0.41333333333333333, 6.575878401988876, 1.6486448190828538, 'UPHENO:0087924', 'abnormal camera-type eye morphology'),
(53798, 'HP:0030502', 'Retinoschisis', 'XPO:0129432', 'decreased size of the retinal stem cell', 0.4574468085106383, 8.040873045973026, 1.9178820903589395, 'HP:0000479', 'Abnormal retinal morphology'),
(53799, 'HP:0030502', 'Retinoschisis', 'XPO:0141338', 'decreased pigmentation in the optic nerve', 0.41836734693877553, 7.796308075334707, 1.8060234564908433, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(53800, 'HP:0030502', 'Retinoschisis', 'XPO:0128330', 'decreased size of the retinal progenitor cell region', 0.5584415584415584, 8.040873045973026, 2.1190464070010115, 'HP:0000479', 'Abnormal retinal morphology'),
(53801, 'HP:0030502', 'Retinoschisis', 'XPO:0140489', 'abnormally necrotic ciliary marginal zone', 0.5119047619047619, 8.040873045973026, 2.028832472656439, 'HP:0000479', 'Abnormal retinal morphology'),
(53802, 'HP:0030502', 'Retinoschisis', 'XPO:0103048', 'abnormal cornea morphology', 0.45454545454545453, 6.887869297006056, 1.769420718895678, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(53803, 'HP:0030502', 'Retinoschisis', 'XPO:0102996', 'abnormal optic fiber layer morphology', 0.524390243902439, 8.040873045973026, 2.053425279323877, 'HP:0000479', 'Abnormal retinal morphology'),
(53804, 'HP:0030502', 'Retinoschisis', 'XPO:0102862', 'abnormal iris morphology', 0.4430379746835443, 6.887869297006056, 1.7468794071802813, 'HP:0012372', 'Abnormal eye morphology'),
(53805, 'HP:0030502', 'Retinoschisis', 'XPO:0102117', 'abnormal retina morphology', 0.6323529411764706, 8.040873045973026, 2.2549212226256703, 'HP:0000479', 'Abnormal retinal morphology'),
(53806, 'HP:0030502', 'Retinoschisis', 'XPO:0140250', 'abnormally necrotic iris', 0.4166666666666667, 6.887869297006056, 1.6940913612964297, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(53807, 'HP:0030502', 'Retinoschisis', 'XPO:0101823', 'abnormal lens epithelium morphology', 0.4268292682926829, 6.887869297006056, 1.714626551799759, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(53808, 'HP:0030502', 'Retinoschisis', 'XPO:0130734', 'increased size of the amacrine cell', 0.4174757281553398, 8.040873045973026, 1.8321761186829812, 'HP:0000479', 'Abnormal retinal morphology'),
(53809, 'HP:0030502', 'Retinoschisis', 'XPO:0128643', 'decreased size of the retinal layer', 0.589041095890411, 8.040873045973026, 2.1763282544036455, 'HP:0000479', 'Abnormal retinal morphology'),
(53810, 'HP:0030502', 'Retinoschisis', 'XPO:0102882', 'abnormal retinal cone cell morphology', 0.4942528735632184, 8.040873045973026, 1.9935457378573478, 'HP:0000479', 'Abnormal retinal morphology'),
(53811, 'HP:0030502', 'Retinoschisis', 'XPO:0140820', 'abnormally necrotic globe', 0.4246575342465753, 6.575878401988876, 1.6710763919384135, 'UPHENO:0087924', 'abnormal camera-type eye morphology'),
(53812, 'HP:0030502', 'Retinoschisis', 'XPO:0140240', 'abnormally necrotic eye photoreceptor cell', 0.48314606741573035, 8.040873045973026, 1.9710190741722953, 'HP:0000479', 'Abnormal retinal morphology'),
(53813, 'HP:0030502', 'Retinoschisis', 'XPO:0129285', 'decreased size of the retinal inner plexiform layer', 0.4777777777777778, 8.040873045973026, 1.960038381077836, 'HP:0000479', 'Abnormal retinal morphology'),
(53814, 'HP:0030502', 'Retinoschisis', 'XPO:0130560', 'increased size of the bipolar neuron', 0.4174757281553398, 8.040873045973026, 1.8321761186829812, 'HP:0000479', 'Abnormal retinal morphology'),
(53815, 'HP:0030502', 'Retinoschisis', 'XPO:0141343', 'decreased pigmentation in the eye', 0.4861111111111111, 6.887869297006056, 1.8298278053291577, 'HP:0012372', 'Abnormal eye morphology'),
(53816, 'HP:0030502', 'Retinoschisis', 'XPO:0130125', 'increased size of the outer limiting membrane', 0.4777777777777778, 8.040873045973026, 1.960038381077836, 'HP:0000479', 'Abnormal retinal morphology'),
(53817, 'HP:0030502', 'Retinoschisis', 'XPO:0140464', 'abnormally necrotic retinal pigmented epithelium', 0.4777777777777778, 8.040873045973026, 1.960038381077836, 'HP:0000479', 'Abnormal retinal morphology'),
(53818, 'HP:0030502', 'Retinoschisis', 'XPO:0101817', 'abnormal eye morphology', 0.5072463768115942, 6.887869297006056, 1.8691834433404724, 'HP:0012372', 'Abnormal eye morphology'),
(53819, 'HP:0030502', 'Retinoschisis', 'XPO:0141181', 'abnormally necrotic choroid', 0.41333333333333333, 6.575878401988876, 1.6486448190828538, 'UPHENO:0087924', 'abnormal camera-type eye morphology'),
(53820, 'HP:0030502', 'Retinoschisis', 'XPO:0128467', 'decreased size of the lens', 0.43209876543209874, 6.887869297006056, 1.7251781994025936, 'HP:0012372', 'Abnormal eye morphology'),
(53821, 'HP:0030502', 'Retinoschisis', 'XPO:0140192', 'abnormally necrotic retina', 0.589041095890411, 8.040873045973026, 2.1763282544036455, 'HP:0000479', 'Abnormal retinal morphology'),
(53822, 'HP:0030502', 'Retinoschisis', 'XPO:0140945', 'abnormally necrotic retinal ganglion cell layer', 0.48314606741573035, 8.040873045973026, 1.9710190741722953, 'HP:0000479', 'Abnormal retinal morphology'),
(53823, 'HP:0030502', 'Retinoschisis', 'XPO:0125932', 'absent retinal pigmented epithelium', 0.40625, 7.796308075334707, 1.7796769806919246, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(53824, 'HP:0030502', 'Retinoschisis', 'XPO:0128475', 'decreased size of the retinal stem cell region', 0.5584415584415584, 8.040873045973026, 2.1190464070010115, 'HP:0000479', 'Abnormal retinal morphology'),
(53825, 'HP:0030502', 'Retinoschisis', 'XPO:0140006', 'abnormally necrotic retinal neural layer', 0.48314606741573035, 8.040873045973026, 1.9710190741722953, 'HP:0000479', 'Abnormal retinal morphology'),
(53826, 'HP:0030502', 'Retinoschisis', 'XPO:0141337', 'increased pigmentation in the eye', 0.4861111111111111, 6.887869297006056, 1.8298278053291577, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(53827, 'HP:0030502', 'Retinoschisis', 'XPO:0102550', 'abnormal lens morphology', 0.4794520547945205, 6.887869297006056, 1.81725152018251, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(53828, 'HP:0030502', 'Retinoschisis', 'XPO:0103814', 'decreased length of axon in retinal ganglion cell', 0.43, 8.040873045973026, 1.859455675666511, 'HP:0000479', 'Abnormal retinal morphology'),
(53829, 'HP:0030502', 'Retinoschisis', 'XPO:0128568', 'decreased size of the optic disc', 0.43661971830985913, 6.575878401988876, 1.6944492248268372, 'UPHENO:0087924', 'abnormal camera-type eye morphology'),
(53830, 'HP:0030502', 'Retinoschisis', 'XPO:0141014', 'abnormally necrotic retinal outer plexiform layer', 0.48314606741573035, 8.040873045973026, 1.9710190741722953, 'HP:0000479', 'Abnormal retinal morphology'),
(53831, 'HP:0030502', 'Retinoschisis', 'XPO:0102476', 'abnormal lens transitional zone morphology', 0.4666666666666667, 6.887869297006056, 1.7928577760852904, 'HP:0012372', 'Abnormal eye morphology'),
(53832, 'HP:0030502', 'Retinoschisis', 'XPO:0128521', 'decreased size of the horizontal cell', 0.43434343434343436, 8.040873045973026, 1.8688232698432123, 'HP:0000479', 'Abnormal retinal morphology'),
(53833, 'HP:0030502', 'Retinoschisis', 'XPO:0140538', 'abnormally necrotic optic disc', 0.4492753623188406, 6.575878401988876, 1.7188310421964663, 'UPHENO:0087924', 'abnormal camera-type eye morphology'),
(53834, 'HP:0030502', 'Retinoschisis', 'XPO:0129955', 'increased size of the retinal stem cell region', 0.5584415584415584, 8.040873045973026, 2.1190464070010115, 'HP:0000479', 'Abnormal retinal morphology'),
(53835, 'HP:0030502', 'Retinoschisis', 'XPO:0128491', 'decreased size of the retinal ganglion cell', 0.42574257425742573, 8.040873045973026, 1.850227550835222, 'HP:0000479', 'Abnormal retinal morphology'),
(53836, 'HP:0030502', 'Retinoschisis', 'XPO:0140520', 'abnormally necrotic retinal outer nuclear layer', 0.48314606741573035, 8.040873045973026, 1.9710190741722953, 'HP:0000479', 'Abnormal retinal morphology'),
(53837, 'HP:0030502', 'Retinoschisis', 'XPO:0129388', 'decreased size of the sclera', 0.45454545454545453, 6.887869297006056, 1.769420718895678, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(53838, 'HP:0030502', 'Retinoschisis', 'XPO:0127230', 'abnormally localised hyaloid blood vessel', 0.4189189189189189, 6.887869297006056, 1.6986638159319787, 'HP:0012372', 'Abnormal eye morphology'),
(53839, 'HP:0030502', 'Retinoschisis', 'XPO:0102212', 'abnormal globe morphology', 0.45588235294117646, 6.575878401988876, 1.7314233793482612, 'UPHENO:0087924', 'abnormal camera-type eye morphology'),
(53840, 'HP:0030502', 'Retinoschisis', 'XPO:0125909', 'absent retinal blood vessel', 0.524390243902439, 8.040873045973026, 2.053425279323877, 'HP:0000479', 'Abnormal retinal morphology'),
(53841, 'HP:0030502', 'Retinoschisis', 'XPO:0129981', 'increased size of the retinal ganglion cell layer', 0.4777777777777778, 8.040873045973026, 1.960038381077836, 'HP:0000479', 'Abnormal retinal morphology'),
(53842, 'HP:0030502', 'Retinoschisis', 'XPO:0141156', 'abnormally necrotic outer limiting membrane', 0.48314606741573035, 8.040873045973026, 1.9710190741722953, 'HP:0000479', 'Abnormal retinal morphology'),
(53843, 'HP:0030502', 'Retinoschisis', 'XPO:0102723', 'abnormal lower eyelid morphology', 0.40789473684210525, 6.575878401988876, 1.6377625561371638, 'UPHENO:0087924', 'abnormal camera-type eye morphology'),
(53844, 'HP:0030502', 'Retinoschisis', 'XPO:0129775', 'increased size of the retinal neural layer', 0.4777777777777778, 8.040873045973026, 1.960038381077836, 'HP:0000479', 'Abnormal retinal morphology'),
(53845, 'HP:0030502', 'Retinoschisis', 'XPO:0140491', 'abnormally necrotic retinal rod cell', 0.4673913043478261, 8.040873045973026, 1.938616553383523, 'HP:0000479', 'Abnormal retinal morphology'),
(53846, 'HP:0030502', 'Retinoschisis', 'XPO:0130893', 'increased size of the pupil', 0.4166666666666667, 6.887869297006056, 1.6940913612964297, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(53847, 'HP:0030502', 'Retinoschisis', 'XPO:0128431', 'decreased size of the retinal inner nuclear layer', 0.4777777777777778, 8.040873045973026, 1.960038381077836, 'HP:0000479', 'Abnormal retinal morphology'),
(53848, 'HP:0030502', 'Retinoschisis', 'XPO:0133372', 'eye fused with olfactory epithelium', 0.4861111111111111, 6.887869297006056, 1.8298278053291577, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(53849, 'HP:0030502', 'Retinoschisis', 'XPO:0130906', 'increased size of the retinal stem cell', 0.4574468085106383, 8.040873045973026, 1.9178820903589395, 'HP:0000479', 'Abnormal retinal morphology'),
(53850, 'HP:0030502', 'Retinoschisis', 'XPO:0102946', 'abnormal retinal inner nuclear layer morphology', 0.524390243902439, 8.040873045973026, 2.053425279323877, 'HP:0000479', 'Abnormal retinal morphology'),
(53851, 'HP:0030502', 'Retinoschisis', 'XPO:0128052', 'decreased size of the iris', 0.4069767441860465, 6.887869297006056, 1.6742767456052652, 'HP:0012372', 'Abnormal eye morphology'),
(53852, 'HP:0030502', 'Retinoschisis', 'XPO:0100710', 'abnormal hyaloid vein', 0.4626865671641791, 6.887869297006056, 1.7851959556606887, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(53853, 'HP:0030502', 'Retinoschisis', 'XPO:0140553', 'abnormally necrotic retinal stem cell region', 0.5733333333333334, 8.040873045973026, 2.147114469784475, 'HP:0000479', 'Abnormal retinal morphology'),
(53854, 'HP:0030502', 'Retinoschisis', 'XPO:0141141', 'abnormally necrotic cornea', 0.42168674698795183, 6.887869297006056, 1.7042661756699493, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(53855, 'HP:0030502', 'Retinoschisis', 'XPO:0140487', 'abnormally necrotic retinal layer', 0.5972222222222222, 8.040873045973026, 2.191389529299339, 'HP:0000479', 'Abnormal retinal morphology'),
(53856, 'HP:0030502', 'Retinoschisis', 'XPO:0133371', 'eye fused with olfactory pit', 0.4861111111111111, 6.887869297006056, 1.8298278053291577, 'HP:0012372', 'Abnormal eye morphology'),
(53857, 'HP:0030502', 'Retinoschisis', 'XPO:0129681', 'increased size of the eye photoreceptor cell', 0.44329896907216493, 8.040873045973026, 1.8879911895239345, 'HP:0000479', 'Abnormal retinal morphology'),
(53858, 'HP:0030502', 'Retinoschisis', 'XPO:0130362', 'increased size of the retinal pigmented epithelium', 0.4725274725274725, 8.040873045973026, 1.9492391893577128, 'HP:0000479', 'Abnormal retinal morphology'),
(53859, 'HP:0030502', 'Retinoschisis', 'XPO:0130863', 'increased size of the sclera', 0.45454545454545453, 6.887869297006056, 1.769420718895678, 'HP:0012372', 'Abnormal eye morphology'),
(53860, 'HP:0030502', 'Retinoschisis', 'XPO:0130614', 'increased size of the retinal progenitor cell', 0.4574468085106383, 8.040873045973026, 1.9178820903589395, 'HP:0000479', 'Abnormal retinal morphology'),
(53861, 'HP:0030502', 'Retinoschisis', 'XPO:0102162', 'abnormal ciliary marginal zone morphology', 0.5657894736842105, 8.040873045973026, 2.1329419421640696, 'HP:0000479', 'Abnormal retinal morphology'),
(53862, 'HP:0030502', 'Retinoschisis', 'XPO:0101961', 'abnormal retinal blood vessel morphology', 0.5058823529411764, 8.040873045973026, 2.0168628550791743, 'HP:0000479', 'Abnormal retinal morphology'),
(53863, 'HP:0030502', 'Retinoschisis', 'XPO:0140531', 'abnormally necrotic retinal progenitor cell region', 0.5733333333333334, 8.040873045973026, 2.147114469784475, 'HP:0000479', 'Abnormal retinal morphology'),
(53864, 'HP:0030502', 'Retinoschisis', 'XPO:0140799', 'abnormally necrotic ciliary body', 0.42168674698795183, 6.887869297006056, 1.7042661756699493, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(53865, 'HP:0030502', 'Retinoschisis', 'XPO:0130326', 'increased size of the retinal cone cell', 0.43, 8.040873045973026, 1.859455675666511, 'HP:0000479', 'Abnormal retinal morphology'),
(53866, 'HP:0030502', 'Retinoschisis', 'XPO:0140808', 'abnormally necrotic retinal cone cell', 0.4673913043478261, 8.040873045973026, 1.938616553383523, 'HP:0000479', 'Abnormal retinal morphology'),
(53867, 'HP:0030502', 'Retinoschisis', 'XPO:0129947', 'increased size of the lens', 0.43209876543209874, 6.887869297006056, 1.7251781994025936, 'HP:0012372', 'Abnormal eye morphology'),
(53868, 'HP:0030502', 'Retinoschisis', 'XPO:0130396', 'increased size of the choroid', 0.4025974025974026, 6.575878401988876, 1.627092979653308, 'UPHENO:0087924', 'abnormal camera-type eye morphology'),
(53869, 'HP:0030502', 'Retinoschisis', 'XPO:0128501', 'decreased size of the retinal ganglion cell layer', 0.4777777777777778, 8.040873045973026, 1.960038381077836, 'HP:0000479', 'Abnormal retinal morphology'),
(53870, 'HP:0030502', 'Retinoschisis', 'XPO:0100329', 'abnormal retinal blood vessel', 0.6417910447761194, 8.040873045973026, 2.2716866670135576, 'HP:0000479', 'Abnormal retinal morphology'),
(53871, 'HP:0030502', 'Retinoschisis', 'XPO:0140439', 'abnormally necrotic retinal stem cell', 0.5, 8.040873045973026, 2.0051026215599324, 'HP:0000479', 'Abnormal retinal morphology'),
(53872, 'HP:0030502', 'Retinoschisis', 'XPO:0102831', 'abnormal optic disc morphology', 0.4696969696969697, 6.575878401988876, 1.757461282222151, 'UPHENO:0087924', 'abnormal camera-type eye morphology'),
(53873, 'HP:0030502', 'Retinoschisis', 'XPO:0133370', 'olfactory pit fused with brain', 0.4307692307692308, 5.788671267106304, 1.5791078078799214, 'UPHENO:0087472', 'abnormal face morphology'),
(53874, 'HP:0030502', 'Retinoschisis', 'XPO:0102450', 'abnormal retinal stem cell morphology', 0.5308641975308642, 8.040873045973026, 2.066061861851679, 'HP:0000479', 'Abnormal retinal morphology'),
(53875, 'HP:0030502', 'Retinoschisis', 'XPO:0130079', 'increased size of the olfactory pit', 0.417910447761194, 5.788671267106304, 1.5553604730668558, 'UPHENO:0087472', 'abnormal face morphology'),
(53876, 'HP:0030502', 'Retinoschisis', 'XPO:0102784', 'abnormal retinal progenitor cell region morphology', 0.5972222222222222, 8.040873045973026, 2.191389529299339, 'HP:0000479', 'Abnormal retinal morphology'),
(53877, 'HP:0030502', 'Retinoschisis', 'XPO:0129029', 'decreased size of the Muller cell', 0.48314606741573035, 8.040873045973026, 1.9710190741722953, 'HP:0000479', 'Abnormal retinal morphology'),
(53878, 'HP:0030502', 'Retinoschisis', 'XPO:0128200', 'decreased size of the retinal rod cell', 0.43, 8.040873045973026, 1.859455675666511, 'HP:0000479', 'Abnormal retinal morphology'),
(53879, 'HP:0011548', 'Absent right sided atrioventricular connection', 'XPO:0141328', 'edematous circulatory system', 0.4473684210526316, 5.9590888072311134, 1.6327608981732116, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(53880, 'HP:0011548', 'Absent right sided atrioventricular connection', 'XPO:0102532', 'abnormal angioblast morphology', 0.425, 5.9590888072311134, 1.5914184688739863, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(53881, 'HP:0011548', 'Absent right sided atrioventricular connection', 'XPO:0101713', 'abnormal anatomical entity in vitro morphology', 0.4074074074074074, 2.485033483301678, 1.006191357919822, 'UPHENO:0076692', 'abnormal anatomical entity morphology'),
(53882, 'HP:0011548', 'Absent right sided atrioventricular connection', 'XPO:0101638', 'abnormal anatomical structure morphology', 0.4074074074074074, 2.485033483301678, 1.006191357919822, 'UPHENO:0076692', 'abnormal anatomical entity morphology'),
(53883, 'HP:0011548', 'Absent right sided atrioventricular connection', 'XPO:0100054', 'abnormal blood vessel', 0.4117647058823529, 5.249153838287537, 1.4701755971154233, 'UPHENO:0080362', 'abnormal cardiovascular system'),
(53884, 'HP:0011548', 'Absent right sided atrioventricular connection', 'XPO:0102935', 'abnormal bulbous arteriosis morphology', 0.4473684210526316, 5.9590888072311134, 1.6327608981732116, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(53885, 'HP:0011548', 'Absent right sided atrioventricular connection', 'XPO:0102113', 'abnormal anatomical line morphology', 0.4074074074074074, 2.485033483301678, 1.006191357919822, 'UPHENO:0076692', 'abnormal anatomical entity morphology'),
(53886, 'HP:0011548', 'Absent right sided atrioventricular connection', 'XPO:0139990', 'abnormally necrotic cardiovascular system', 0.4146341463414634, 5.9590888072311134, 1.57189112236161, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(53887, 'HP:0011548', 'Absent right sided atrioventricular connection', 'XPO:0101995', 'abnormal cardiovascular system morphology', 0.4857142857142857, 5.9590888072311134, 1.7012979055745219, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(53888, 'HP:0011548', 'Absent right sided atrioventricular connection', 'XPO:0101919', 'abnormal heart primordium morphology', 0.425, 5.9590888072311134, 1.5914184688739863, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(53889, 'HP:0011548', 'Absent right sided atrioventricular connection', 'XPO:0101900', 'abnormal circulatory system morphology', 0.4857142857142857, 5.9590888072311134, 1.7012979055745219, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(53890, 'HP:0011548', 'Absent right sided atrioventricular connection', 'XPO:0102800', 'abnormal circulating cell morphology', 0.425, 5.9590888072311134, 1.5914184688739863, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(53891, 'HP:0011548', 'Absent right sided atrioventricular connection', 'XPO:0101770', 'abnormal trunk vasculature morphology', 0.40476190476190477, 5.9590888072311134, 1.5530653998657664, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(53892, 'HP:0011548', 'Absent right sided atrioventricular connection', 'XPO:0139811', 'abnormally necrotic circulatory system', 0.4146341463414634, 5.9590888072311134, 1.57189112236161, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(53893, 'HP:0011548', 'Absent right sided atrioventricular connection', 'XPO:0101976', 'abnormal portion of organism substance morphology', 0.4074074074074074, 2.485033483301678, 1.006191357919822, 'UPHENO:0076692', 'abnormal anatomical entity morphology'),
(53894, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0128200', 'decreased size of the retinal rod cell', 0.45714285714285713, 9.027174500716514, 2.0314301226438216, 'UPHENO:0088016', 'abnormal layer of retina morphology'),
(53895, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0128201', 'decreased size of the eye photoreceptor cell', 0.47058823529411764, 9.027174500716514, 2.0610876056063803, 'UPHENO:0088016', 'abnormal layer of retina morphology'),
(53896, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0130506', 'increased size of the Muller cell', 0.4639175257731959, 8.767034997756374, 2.016725361700535, 'UPHENO:0015314', 'abnormal anatomical entity morphology in the retina'),
(53897, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0129038', 'decreased size of the retinal outer nuclear layer', 0.5052631578947369, 9.027174500716514, 2.1356728904724314, 'UPHENO:0088016', 'abnormal layer of retina morphology'),
(53898, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0129062', 'decreased size of the ciliary body', 0.41304347826086957, 6.887869297006056, 1.68670966447745, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(53899, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0103186', 'abnormal peripheral retina morphology', 0.55, 8.767034997756374, 2.1958755084853983, 'UPHENO:0015314', 'abnormal anatomical entity morphology in the retina'),
(53900, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0140081', 'abnormally necrotic amacrine cell', 0.4368932038834951, 9.027174500716514, 1.9859282941822014, 'UPHENO:0088016', 'abnormal layer of retina morphology'),
(53901, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0102196', 'abnormal central retina morphology', 0.5714285714285714, 8.767034997756374, 2.238243571292502, 'UPHENO:0015314', 'abnormal anatomical entity morphology in the retina'),
(53902, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0129971', 'increased size of the retinal ganglion cell', 0.42592592592592593, 9.027174500716514, 1.9608436086829029, 'UPHENO:0088016', 'abnormal layer of retina morphology'),
(53903, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0140391', 'abnormally necrotic central retina', 0.55, 8.767034997756374, 2.1958755084853983, 'UPHENO:0015314', 'abnormal anatomical entity morphology in the retina'),
(53904, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0128848', 'decreased size of the retinal cone cell', 0.45714285714285713, 9.027174500716514, 2.0314301226438216, 'UPHENO:0088016', 'abnormal layer of retina morphology'),
(53905, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0130353', 'increased size of the photoreceptor layer', 0.4791666666666667, 9.027174500716514, 2.0797887188189725, 'UPHENO:0088016', 'abnormal layer of retina morphology'),
(53906, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0133372', 'eye fused with olfactory epithelium', 0.4268292682926829, 6.887869297006056, 1.714626551799759, 'HP:0012372', 'Abnormal eye morphology'),
(53907, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0128467', 'decreased size of the lens', 0.4318181818181818, 6.887869297006056, 1.7246179856520207, 'HP:0012372', 'Abnormal eye morphology'),
(53908, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0102963', 'abnormal retinal outer nuclear layer morphology', 0.5, 9.027174500716514, 2.124520475391625, 'UPHENO:0088016', 'abnormal layer of retina morphology'),
(53909, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0130515', 'increased size of the retinal outer nuclear layer', 0.4742268041237113, 9.027174500716514, 2.0690403847537273, 'UPHENO:0088016', 'abnormal layer of retina morphology'),
(53910, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0103336', 'decreased size of the eye', 0.4367816091954023, 6.887869297006056, 1.7345012641891933, 'HP:0012372', 'Abnormal eye morphology'),
(53911, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0140808', 'abnormally necrotic retinal cone cell', 0.45, 9.027174500716514, 2.0154970913703725, 'UPHENO:0088016', 'abnormal layer of retina morphology'),
(53912, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0140489', 'abnormally necrotic ciliary marginal zone', 0.4731182795698925, 8.767034997756374, 2.036625767063633, 'UPHENO:0015314', 'abnormal anatomical entity morphology in the retina'),
(53913, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0129432', 'decreased size of the retinal stem cell', 0.47, 8.767034997756374, 2.029903063928299, 'UPHENO:0015314', 'abnormal anatomical entity morphology in the retina'),
(53914, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0128568', 'decreased size of the optic disc', 0.4358974358974359, 6.575878401988876, 1.6930471151743767, 'UPHENO:0087924', 'abnormal camera-type eye morphology'),
(53915, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0128807', 'decreased size of the lens transitional zone', 0.42696629213483145, 6.887869297006056, 1.7149017506702897, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(53916, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0100779', 'abnormal optic choroid vascular plexus', 0.40789473684210525, 6.887869297006056, 1.6761639640277146, 'HP:0012372', 'Abnormal eye morphology'),
(53917, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0129911', 'increased size of the retinal inner nuclear layer', 0.4742268041237113, 9.027174500716514, 2.0690403847537273, 'UPHENO:0088016', 'abnormal layer of retina morphology'),
(53918, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0140491', 'abnormally necrotic retinal rod cell', 0.45, 9.027174500716514, 2.0154970913703725, 'UPHENO:0088016', 'abnormal layer of retina morphology'),
(53919, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0140520', 'abnormally necrotic retinal outer nuclear layer', 0.4639175257731959, 9.027174500716514, 2.046427242560871, 'UPHENO:0088016', 'abnormal layer of retina morphology'),
(53920, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0129741', 'increased size of the optic fiber layer', 0.4742268041237113, 9.027174500716514, 2.0690403847537273, 'UPHENO:0088016', 'abnormal layer of retina morphology'),
(53921, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0102550', 'abnormal lens morphology', 0.42168674698795183, 6.887869297006056, 1.7042661756699493, 'HP:0012372', 'Abnormal eye morphology'),
(53922, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0141333', 'increased pigmentation in the retinal pigmented epithelium', 0.5, 11.964122330181212, 2.4458252523617885, 'UPHENO:0088021', 'abnormal pigmented layer of retina morphology'),
(53923, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0129681', 'increased size of the eye photoreceptor cell', 0.4423076923076923, 9.027174500716514, 1.9981963670947773, 'UPHENO:0088016', 'abnormal layer of retina morphology'),
(53924, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0102239', 'abnormal retinal pigmented epithelium morphology', 0.5168539325842697, 11.964122330181212, 2.4867053859018835, 'UPHENO:0088021', 'abnormal pigmented layer of retina morphology'),
(53925, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0102266', 'abnormal horizontal cell morphology', 0.4787234042553192, 9.027174500716514, 2.0788265218122026, 'UPHENO:0088016', 'abnormal layer of retina morphology'),
(53926, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0140869', 'abnormally necrotic optic chiasm', 0.4270833333333333, 7.796308075334707, 1.8247392253435917, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(53927, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0129775', 'increased size of the retinal neural layer', 0.4742268041237113, 9.027174500716514, 2.0690403847537273, 'UPHENO:0088016', 'abnormal layer of retina morphology'),
(53928, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0102996', 'abnormal optic fiber layer morphology', 0.5, 9.027174500716514, 2.124520475391625, 'UPHENO:0088016', 'abnormal layer of retina morphology'),
(53929, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0102882', 'abnormal retinal cone cell morphology', 0.47368421052631576, 9.027174500716514, 2.067856384436596, 'UPHENO:0088016', 'abnormal layer of retina morphology'),
(53930, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0102117', 'abnormal retina morphology', 0.5512820512820513, 8.040873045973026, 2.1054189575670126, 'HP:0000479', 'Abnormal retinal morphology'),
(53931, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0102441', 'abnormal retinal inner plexiform layer morphology', 0.5, 9.027174500716514, 2.124520475391625, 'UPHENO:0088016', 'abnormal layer of retina morphology'),
(53932, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0140464', 'abnormally necrotic retinal pigmented epithelium', 0.4742268041237113, 11.964122330181212, 2.381954553887829, 'UPHENO:0088021', 'abnormal pigmented layer of retina morphology'),
(53933, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0103048', 'abnormal cornea morphology', 0.40229885057471265, 6.887869297006056, 1.6646266551675757, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(53934, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0128599', 'decreased size of the olfactory pit', 0.4189189189189189, 5.788671267106304, 1.5572359837844685, 'UPHENO:0087472', 'abnormal face morphology'),
(53935, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0133369', 'eye fused with brain', 0.4268292682926829, 6.887869297006056, 1.714626551799759, 'HP:0012372', 'Abnormal eye morphology'),
(53936, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0128052', 'decreased size of the iris', 0.40860215053763443, 6.887869297006056, 1.6776168237648366, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(53937, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0102851', 'abnormal retinal rod cell morphology', 0.47368421052631576, 9.027174500716514, 2.067856384436596, 'UPHENO:0088016', 'abnormal layer of retina morphology'),
(53938, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0100371', 'abnormal hyaloid blood vessel', 0.41333333333333333, 6.887869297006056, 1.6873013886368484, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(53939, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0128295', 'decreased size of the retinal neural layer', 0.5052631578947369, 9.027174500716514, 2.1356728904724314, 'UPHENO:0088016', 'abnormal layer of retina morphology'),
(53940, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0103086', 'abnormal amacrine cell morphology', 0.4639175257731959, 9.027174500716514, 2.046427242560871, 'UPHENO:0088016', 'abnormal layer of retina morphology'),
(53941, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0102663', 'abnormal retinal progenitor cell morphology', 0.4888888888888889, 8.767034997756374, 2.0702912835886442, 'UPHENO:0015314', 'abnormal anatomical entity morphology in the retina'),
(53942, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0141156', 'abnormally necrotic outer limiting membrane', 0.4639175257731959, 9.027174500716514, 2.046427242560871, 'UPHENO:0088016', 'abnormal layer of retina morphology'),
(53943, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0103926', 'decreased pigmentation in the retinal pigmented epithelium', 0.5, 11.964122330181212, 2.4458252523617885, 'UPHENO:0088021', 'abnormal pigmented layer of retina morphology'),
(53944, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0115417', 'abnormally wholly ventralized eye', 0.4069767441860465, 6.887869297006056, 1.6742767456052652, 'HP:0012372', 'Abnormal eye morphology'),
(53945, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0102815', 'abnormal retinal ganglion cell morphology', 0.46875, 9.027174500716514, 2.057058104967107, 'UPHENO:0088016', 'abnormal layer of retina morphology'),
(53946, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0139731', 'abnormally necrotic eye', 0.4069767441860465, 6.887869297006056, 1.6742767456052652, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(53947, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0128779', 'decreased size of the retinal blood vessel', 0.47, 8.767034997756374, 2.029903063928299, 'UPHENO:0015314', 'abnormal anatomical entity morphology in the retina'),
(53948, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0141638', 'neoplastic eye', 0.4268292682926829, 6.887869297006056, 1.714626551799759, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(53949, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0128521', 'decreased size of the horizontal cell', 0.46153846153846156, 9.027174500716514, 2.041173248673402, 'UPHENO:0088016', 'abnormal layer of retina morphology'),
(53950, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0128884', 'decreased size of the retinal pigmented epithelium', 0.5157894736842106, 11.964122330181212, 2.4841433855109245, 'UPHENO:0088021', 'abnormal pigmented layer of retina morphology'),
(53951, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0103226', 'abnormal retinal outer plexiform layer morphology', 0.5, 9.027174500716514, 2.124520475391625, 'UPHENO:0088016', 'abnormal layer of retina morphology'),
(53952, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0102232', 'abnormal eye photoreceptor cell morphology', 0.4838709677419355, 9.027174500716514, 2.0899731246207502, 'UPHENO:0088016', 'abnormal layer of retina morphology'),
(53953, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0128787', 'decreased size of the peripheral retina', 0.5529411764705883, 8.767034997756374, 2.201739004927294, 'UPHENO:0015314', 'abnormal anatomical entity morphology in the retina'),
(53954, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0141343', 'decreased pigmentation in the eye', 0.4268292682926829, 6.887869297006056, 1.714626551799759, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(53955, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0102805', 'abnormal retinal layer morphology', 0.6081081081081081, 9.027174500716514, 2.3429677776684157, 'UPHENO:0088016', 'abnormal layer of retina morphology'),
(53956, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0130362', 'increased size of the retinal pigmented epithelium', 0.4845360824742268, 11.964122330181212, 2.4077061623272105, 'UPHENO:0088021', 'abnormal pigmented layer of retina morphology'),
(53957, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0103814', 'decreased length of axon in retinal ganglion cell', 0.45714285714285713, 9.027174500716514, 2.0314301226438216, 'UPHENO:0088016', 'abnormal layer of retina morphology'),
(53958, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0103780', 'decreased size of the bipolar neuron in the retinal inner plexiform layer', 0.43243243243243246, 9.027174500716514, 1.9757639098173827, 'UPHENO:0088016', 'abnormal layer of retina morphology'),
(53959, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0139912', 'abnormally necrotic optic fiber layer', 0.4639175257731959, 9.027174500716514, 2.046427242560871, 'UPHENO:0088016', 'abnormal layer of retina morphology'),
(53960, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0139887', 'abnormally necrotic Muller cell', 0.4888888888888889, 8.767034997756374, 2.0702912835886442, 'UPHENO:0015314', 'abnormal anatomical entity morphology in the retina'),
(53961, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0128475', 'decreased size of the retinal stem cell region', 0.5662650602409639, 8.767034997756374, 2.2281080766289487, 'UPHENO:0015314', 'abnormal anatomical entity morphology in the retina'),
(53962, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0130863', 'increased size of the sclera', 0.4186046511627907, 6.887869297006056, 1.698026538169565, 'HP:0012372', 'Abnormal eye morphology'),
(53963, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0140487', 'abnormally necrotic retinal layer', 0.5625, 9.027174500716514, 2.253394252378629, 'UPHENO:0088016', 'abnormal layer of retina morphology'),
(53964, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0128643', 'decreased size of the retinal layer', 0.6153846153846154, 9.027174500716514, 2.3569438491685033, 'UPHENO:0088016', 'abnormal layer of retina morphology'),
(53965, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0128875', 'decreased size of the photoreceptor layer', 0.5106382978723404, 9.027174500716514, 2.1470027996354535, 'UPHENO:0088016', 'abnormal layer of retina morphology'),
(53966, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0141138', 'abnormally necrotic retinal inner plexiform layer', 0.4639175257731959, 9.027174500716514, 2.046427242560871, 'UPHENO:0088016', 'abnormal layer of retina morphology'),
(53967, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0102756', 'abnormal Muller cell morphology', 0.5176470588235295, 8.767034997756374, 2.1303121558099263, 'UPHENO:0015314', 'abnormal anatomical entity morphology in the retina'),
(53968, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0102581', 'abnormal outer limiting membrane morphology', 0.5, 9.027174500716514, 2.124520475391625, 'UPHENO:0088016', 'abnormal layer of retina morphology'),
(53969, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0129258', 'decreased size of the amacrine cell', 0.4444444444444444, 9.027174500716514, 2.0030171132254475, 'UPHENO:0088016', 'abnormal layer of retina morphology'),
(53970, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0103155', 'abnormal bipolar neuron morphology', 0.4639175257731959, 9.027174500716514, 2.046427242560871, 'UPHENO:0088016', 'abnormal layer of retina morphology'),
(53971, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0100329', 'abnormal retinal blood vessel', 0.5584415584415584, 8.040873045973026, 2.1190464070010115, 'HP:0000479', 'Abnormal retinal morphology'),
(53972, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0102162', 'abnormal ciliary marginal zone morphology', 0.5176470588235295, 8.767034997756374, 2.1303121558099263, 'UPHENO:0015314', 'abnormal anatomical entity morphology in the retina'),
(53973, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0100710', 'abnormal hyaloid vein', 0.4025974025974026, 6.887869297006056, 1.6652442128423794, 'HP:0012372', 'Abnormal eye morphology'),
(53974, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0130189', 'increased size of the optic chiasm', 0.42424242424242425, 7.796308075334707, 1.8186601216337221, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(53975, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0129371', 'decreased size of the retinal outer plexiform layer', 0.5052631578947369, 9.027174500716514, 2.1356728904724314, 'UPHENO:0088016', 'abnormal layer of retina morphology'),
(53976, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0130845', 'increased size of the retinal outer plexiform layer', 0.4742268041237113, 9.027174500716514, 2.0690403847537273, 'UPHENO:0088016', 'abnormal layer of retina morphology'),
(53977, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0130761', 'increased size of the retinal inner plexiform layer', 0.4742268041237113, 9.027174500716514, 2.0690403847537273, 'UPHENO:0088016', 'abnormal layer of retina morphology'),
(53978, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0102476', 'abnormal lens transitional zone morphology', 0.4117647058823529, 6.887869297006056, 1.6840966347682629, 'HP:0012372', 'Abnormal eye morphology'),
(53979, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0128646', 'decreased size of the outer limiting membrane', 0.5052631578947369, 9.027174500716514, 2.1356728904724314, 'UPHENO:0088016', 'abnormal layer of retina morphology'),
(53980, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0130122', 'increased size of the retinal layer', 0.575, 9.027174500716514, 2.278294392283841, 'UPHENO:0088016', 'abnormal layer of retina morphology'),
(53981, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0130906', 'increased size of the retinal stem cell', 0.4411764705882353, 8.767034997756374, 1.966674746325303, 'UPHENO:0015314', 'abnormal anatomical entity morphology in the retina'),
(53982, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0101359', 'abnormal hyaloid artery', 0.40229885057471265, 6.887869297006056, 1.6646266551675757, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(53983, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0128501', 'decreased size of the retinal ganglion cell layer', 0.5052631578947369, 9.027174500716514, 2.1356728904724314, 'UPHENO:0088016', 'abnormal layer of retina morphology'),
(53984, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0129388', 'decreased size of the sclera', 0.4523809523809524, 6.887869297006056, 1.765202785080264, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(53985, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0128330', 'decreased size of the retinal progenitor cell region', 0.5662650602409639, 8.767034997756374, 2.2281080766289487, 'UPHENO:0015314', 'abnormal anatomical entity morphology in the retina'),
(53986, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0128261', 'decreased size of the optic fiber layer', 0.5052631578947369, 9.027174500716514, 2.1356728904724314, 'UPHENO:0088016', 'abnormal layer of retina morphology'),
(53987, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0129138', 'decreased size of the retinal progenitor cell', 0.47, 8.767034997756374, 2.029903063928299, 'UPHENO:0015314', 'abnormal anatomical entity morphology in the retina'),
(53988, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0102818', 'abnormal optic chiasm morphology', 0.45054945054945056, 7.796308075334707, 1.8741991141968606, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(53989, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0130001', 'increased size of the horizontal cell', 0.4339622641509434, 9.027174500716514, 1.9792556897017122, 'UPHENO:0088016', 'abnormal layer of retina morphology'),
(53990, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0129029', 'decreased size of the Muller cell', 0.49473684210526314, 8.767034997756374, 2.0826366004217616, 'UPHENO:0015314', 'abnormal anatomical entity morphology in the retina'),
(53991, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0140948', 'abnormally necrotic retinal inner nuclear layer', 0.4639175257731959, 9.027174500716514, 2.046427242560871, 'UPHENO:0088016', 'abnormal layer of retina morphology'),
(53992, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0130560', 'increased size of the bipolar neuron', 0.41818181818181815, 9.027174500716514, 1.94293598601554, 'UPHENO:0088016', 'abnormal layer of retina morphology'),
(53993, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0140797', 'abnormally necrotic bipolar neuron', 0.4368932038834951, 9.027174500716514, 1.9859282941822014, 'UPHENO:0088016', 'abnormal layer of retina morphology'),
(53994, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0102450', 'abnormal retinal stem cell morphology', 0.4888888888888889, 8.767034997756374, 2.0702912835886442, 'UPHENO:0015314', 'abnormal anatomical entity morphology in the retina'),
(53995, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0140553', 'abnormally necrotic retinal stem cell region', 0.5238095238095238, 8.767034997756374, 2.1429550689167978, 'UPHENO:0015314', 'abnormal anatomical entity morphology in the retina'),
(53996, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0133371', 'eye fused with olfactory pit', 0.4268292682926829, 6.887869297006056, 1.714626551799759, 'HP:0012372', 'Abnormal eye morphology'),
(53997, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0102939', 'abnormal retinal ganglion cell layer morphology', 0.5, 9.027174500716514, 2.124520475391625, 'UPHENO:0088016', 'abnormal layer of retina morphology'),
(53998, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0140192', 'abnormally necrotic retina', 0.5180722891566265, 8.040873045973026, 2.0410177622316423, 'HP:0000479', 'Abnormal retinal morphology'),
(53999, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0140531', 'abnormally necrotic retinal progenitor cell region', 0.5238095238095238, 8.767034997756374, 2.1429550689167978, 'UPHENO:0015314', 'abnormal anatomical entity morphology in the retina'),
(54000, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0102513', 'abnormal sclera morphology', 0.4375, 6.887869297006056, 1.7359270772241988, 'HP:0012372', 'Abnormal eye morphology'),
(54001, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0101817', 'abnormal eye morphology', 0.4430379746835443, 6.887869297006056, 1.7468794071802813, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(54002, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0129419', 'decreased size of the pupil', 0.41304347826086957, 6.887869297006056, 1.68670966447745, 'HP:0012372', 'Abnormal eye morphology'),
(54003, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0130265', 'increased size of the peripheral retina', 0.5172413793103449, 8.767034997756374, 2.129477230378755, 'UPHENO:0015314', 'abnormal anatomical entity morphology in the retina'),
(54004, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0103376', 'increased size of the eye', 0.4044943820224719, 6.887869297006056, 1.669162794560202, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(54005, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0140240', 'abnormally necrotic eye photoreceptor cell', 0.4639175257731959, 9.027174500716514, 2.046427242560871, 'UPHENO:0088016', 'abnormal layer of retina morphology'),
(54006, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0130734', 'increased size of the amacrine cell', 0.41818181818181815, 9.027174500716514, 1.94293598601554, 'UPHENO:0088016', 'abnormal layer of retina morphology'),
(54007, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0128918', 'decreased size of the choroid', 0.40476190476190477, 6.575878401988876, 1.6314610223574721, 'UPHENO:0087924', 'abnormal camera-type eye morphology'),
(54008, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0107252', 'decreased size of the globe', 0.4146341463414634, 6.575878401988876, 1.6512370295187557, 'UPHENO:0087924', 'abnormal camera-type eye morphology'),
(54009, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0128935', 'decreased size of the central retina', 0.5949367088607594, 8.767034997756374, 2.283819377278394, 'UPHENO:0015314', 'abnormal anatomical entity morphology in the retina'),
(54010, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0141014', 'abnormally necrotic retinal outer plexiform layer', 0.4639175257731959, 9.027174500716514, 2.046427242560871, 'UPHENO:0088016', 'abnormal layer of retina morphology'),
(54011, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0140317', 'abnormally necrotic retinal progenitor cell', 0.4631578947368421, 8.767034997756374, 2.0150735650702822, 'UPHENO:0015314', 'abnormal anatomical entity morphology in the retina'),
(54012, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0129580', 'increased size of the inner limiting membrane', 0.4742268041237113, 9.027174500716514, 2.0690403847537273, 'UPHENO:0088016', 'abnormal layer of retina morphology'),
(54013, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0130326', 'increased size of the retinal cone cell', 0.42990654205607476, 9.027174500716514, 1.9699851202838587, 'UPHENO:0088016', 'abnormal layer of retina morphology'),
(54014, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0130148', 'increased size of the ciliary marginal zone', 0.4787234042553192, 8.767034997756374, 2.0486543972450444, 'UPHENO:0015314', 'abnormal anatomical entity morphology in the retina'),
(54015, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0129780', 'increased size of the retina', 0.5238095238095238, 8.040873045973026, 2.0522879625491073, 'HP:0000479', 'Abnormal retinal morphology'),
(54016, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0128431', 'decreased size of the retinal inner nuclear layer', 0.5052631578947369, 9.027174500716514, 2.1356728904724314, 'UPHENO:0088016', 'abnormal layer of retina morphology'),
(54017, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0140945', 'abnormally necrotic retinal ganglion cell layer', 0.4639175257731959, 9.027174500716514, 2.046427242560871, 'UPHENO:0088016', 'abnormal layer of retina morphology'),
(54018, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0140006', 'abnormally necrotic retinal neural layer', 0.4639175257731959, 9.027174500716514, 2.046427242560871, 'UPHENO:0088016', 'abnormal layer of retina morphology'),
(54019, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0115423', 'abnormally incomplete structure of eye', 0.4375, 6.887869297006056, 1.7359270772241988, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(54020, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0129981', 'increased size of the retinal ganglion cell layer', 0.4742268041237113, 9.027174500716514, 2.0690403847537273, 'UPHENO:0088016', 'abnormal layer of retina morphology'),
(54021, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0130125', 'increased size of the outer limiting membrane', 0.4742268041237113, 9.027174500716514, 2.0690403847537273, 'UPHENO:0088016', 'abnormal layer of retina morphology'),
(54022, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0130413', 'increased size of the central retina', 0.5555555555555556, 8.767034997756374, 2.206937923629376, 'UPHENO:0015314', 'abnormal anatomical entity morphology in the retina'),
(54023, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0140346', 'abnormally necrotic retinal blood vessel', 0.43564356435643564, 8.767034997756374, 1.9543035524862054, 'UPHENO:0015314', 'abnormal anatomical entity morphology in the retina'),
(54024, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0129810', 'increased size of the retinal progenitor cell region', 0.5294117647058824, 8.767034997756374, 2.1543842436762373, 'UPHENO:0015314', 'abnormal anatomical entity morphology in the retina'),
(54025, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0130257', 'increased size of the retinal blood vessel', 0.4411764705882353, 8.767034997756374, 1.966674746325303, 'UPHENO:0015314', 'abnormal anatomical entity morphology in the retina'),
(54026, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0129680', 'increased size of the retinal rod cell', 0.42990654205607476, 9.027174500716514, 1.9699851202838587, 'UPHENO:0088016', 'abnormal layer of retina morphology'),
(54027, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0128300', 'decreased size of the retina', 0.5609756097560976, 8.040873045973026, 2.1238487846209977, 'HP:0000479', 'Abnormal retinal morphology'),
(54028, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0101961', 'abnormal retinal blood vessel morphology', 0.46808510638297873, 8.767034997756374, 2.0257636855240766, 'UPHENO:0015314', 'abnormal anatomical entity morphology in the retina'),
(54029, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0127563', 'abnormally localised retinal blood vessel', 0.4942528735632184, 8.040873045973026, 1.9935457378573478, 'HP:0000479', 'Abnormal retinal morphology'),
(54030, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0102784', 'abnormal retinal progenitor cell region morphology', 0.5432098765432098, 8.767034997756374, 2.1822786253778963, 'UPHENO:0015314', 'abnormal anatomical entity morphology in the retina'),
(54031, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0101861', 'abnormal photoreceptor layer morphology', 0.5056179775280899, 9.027174500716514, 2.1364226440115797, 'UPHENO:0088016', 'abnormal layer of retina morphology'),
(54032, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0102946', 'abnormal retinal inner nuclear layer morphology', 0.5, 9.027174500716514, 2.124520475391625, 'UPHENO:0088016', 'abnormal layer of retina morphology'),
(54033, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0129083', 'decreased size of the bipolar neuron', 0.4444444444444444, 9.027174500716514, 2.0030171132254475, 'UPHENO:0088016', 'abnormal layer of retina morphology'),
(54034, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0141182', 'abnormally necrotic inner limiting membrane', 0.4639175257731959, 9.027174500716514, 2.046427242560871, 'UPHENO:0088016', 'abnormal layer of retina morphology'),
(54035, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0128491', 'decreased size of the retinal ganglion cell', 0.4528301886792453, 9.027174500716514, 2.0218251982799926, 'UPHENO:0088016', 'abnormal layer of retina morphology'),
(54036, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0103022', 'abnormal ciliary body morphology', 0.40229885057471265, 6.887869297006056, 1.6646266551675757, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(54037, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0103184', 'abnormal inner limiting membrane morphology', 0.5, 9.027174500716514, 2.124520475391625, 'UPHENO:0088016', 'abnormal layer of retina morphology'),
(54038, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0140671', 'abnormally necrotic retinal ganglion cell', 0.44554455445544555, 9.027174500716514, 2.005494562673581, 'UPHENO:0088016', 'abnormal layer of retina morphology'),
(54039, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0130614', 'increased size of the retinal progenitor cell', 0.4411764705882353, 8.767034997756374, 1.966674746325303, 'UPHENO:0015314', 'abnormal anatomical entity morphology in the retina'),
(54040, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0140620', 'abnormally necrotic horizontal cell', 0.45454545454545453, 9.027174500716514, 2.0256507933721757, 'UPHENO:0088016', 'abnormal layer of retina morphology'),
(54041, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0128710', 'decreased size of the optic chiasm', 0.4536082474226804, 7.796308075334707, 1.8805503562574089, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(54042, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0102017', 'abnormal retinal neural layer morphology', 0.5056179775280899, 9.027174500716514, 2.1364226440115797, 'UPHENO:0088016', 'abnormal layer of retina morphology'),
(54043, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0133354', 'fused eyes', 0.4268292682926829, 6.887869297006056, 1.714626551799759, 'HP:0012372', 'Abnormal eye morphology'),
(54044, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0102831', 'abnormal optic disc morphology', 0.40789473684210525, 6.575878401988876, 1.6377625561371638, 'UPHENO:0087924', 'abnormal camera-type eye morphology'),
(54045, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0141323', 'edematous eye', 0.43209876543209874, 6.887869297006056, 1.7251781994025936, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(54046, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0141337', 'increased pigmentation in the eye', 0.4268292682926829, 6.887869297006056, 1.714626551799759, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(54047, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0102505', 'abnormal retinal stem cell region morphology', 0.5432098765432098, 8.767034997756374, 2.1822786253778963, 'UPHENO:0015314', 'abnormal anatomical entity morphology in the retina'),
(54048, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0128669', 'decreased size of the ciliary marginal zone', 0.5108695652173914, 8.767034997756374, 2.1163202398383505, 'UPHENO:0015314', 'abnormal anatomical entity morphology in the retina'),
(54049, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0140218', 'abnormally necrotic sclera', 0.4117647058823529, 6.887869297006056, 1.6840966347682629, 'HP:0012372', 'Abnormal eye morphology'),
(54050, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0125909', 'absent retinal blood vessel', 0.4673913043478261, 8.040873045973026, 1.938616553383523, 'HP:0000479', 'Abnormal retinal morphology'),
(54051, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0140271', 'abnormally necrotic peripheral retina', 0.5116279069767442, 8.767034997756374, 2.1178904046937745, 'UPHENO:0015314', 'abnormal anatomical entity morphology in the retina'),
(54052, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0128100', 'decreased size of the inner limiting membrane', 0.5052631578947369, 9.027174500716514, 2.1356728904724314, 'UPHENO:0088016', 'abnormal layer of retina morphology'),
(54053, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0129955', 'increased size of the retinal stem cell region', 0.5294117647058824, 8.767034997756374, 2.1543842436762373, 'UPHENO:0015314', 'abnormal anatomical entity morphology in the retina'),
(54054, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0141033', 'abnormally necrotic photoreceptor layer', 0.46875, 9.027174500716514, 2.057058104967107, 'UPHENO:0088016', 'abnormal layer of retina morphology'),
(54055, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0140439', 'abnormally necrotic retinal stem cell', 0.4631578947368421, 8.767034997756374, 2.0150735650702822, 'UPHENO:0015314', 'abnormal anatomical entity morphology in the retina'),
(54056, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0101315', 'abnormal hyaloid vascular plexus', 0.4025974025974026, 6.887869297006056, 1.6652442128423794, 'HP:0012372', 'Abnormal eye morphology'),
(54057, 'HP:0007722', 'Retinal pigment epithelial atrophy', 'XPO:0129285', 'decreased size of the retinal inner plexiform layer', 0.5052631578947369, 9.027174500716514, 2.1356728904724314, 'UPHENO:0088016', 'abnormal layer of retina morphology'),
(54058, 'HP:0011131', 'Perianal dermatitis', 'XPO:0102733', 'abnormal posterior foregut morphology', 0.43902439024390244, 5.725717590856133, 1.5854745895265556, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(54059, 'HP:0011131', 'Perianal dermatitis', 'XPO:0141834', 'edematous foregut', 0.42857142857142855, 5.725717590856133, 1.5664861849086864, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(54060, 'HP:0011131', 'Perianal dermatitis', 'XPO:0115391', 'abnormally undifferentiated alimentary system', 0.5, 5.05060299610679, 1.5891197242666757, 'HP:0025031', 'Abnormality of the digestive system'),
(54061, 'HP:0011131', 'Perianal dermatitis', 'XPO:0142061', 'abnormal digestive tract morphology', 0.47368421052631576, 5.725717590856133, 1.6468703703453182, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(54062, 'HP:0011131', 'Perianal dermatitis', 'XPO:0101169', 'abnormal hepato-pancreatic duct', 0.4411764705882353, 5.05060299610679, 1.4927180591674907, 'HP:0025031', 'Abnormality of the digestive system'),
(54063, 'HP:0011131', 'Perianal dermatitis', 'XPO:0102118', 'abnormal oral evagination morphology', 0.46153846153846156, 5.725717590856133, 1.6256195397716668, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(54064, 'HP:0011131', 'Perianal dermatitis', 'XPO:0100718', 'abnormal ventral pancreatic bud', 0.4411764705882353, 5.05060299610679, 1.4927180591674907, 'HP:0025031', 'Abnormality of the digestive system'),
(54065, 'HP:0011131', 'Perianal dermatitis', 'XPO:0140114', 'abnormally necrotic liver and biliary system', 0.4186046511627907, 5.725717590856133, 1.5481640787645816, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(54066, 'HP:0011131', 'Perianal dermatitis', 'XPO:0100462', 'abnormal anterior foregut', 0.45454545454545453, 5.05060299610679, 1.5151662069205463, 'HP:0025031', 'Abnormality of the digestive system'),
(54067, 'HP:0011131', 'Perianal dermatitis', 'XPO:0140542', 'abnormally necrotic larval alimentary system', 0.4090909090909091, 5.725717590856133, 1.5304701939081158, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(54068, 'HP:0011131', 'Perianal dermatitis', 'XPO:0103233', 'abnormal proctodeum morphology', 0.4186046511627907, 5.725717590856133, 1.5481640787645816, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(54069, 'HP:0011131', 'Perianal dermatitis', 'XPO:0141833', 'edematous alimentary system', 0.47368421052631576, 5.725717590856133, 1.6468703703453182, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(54070, 'HP:0011131', 'Perianal dermatitis', 'XPO:0103013', 'abnormal ventral foregut morphology', 0.43902439024390244, 5.725717590856133, 1.5854745895265556, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(54071, 'HP:0011131', 'Perianal dermatitis', 'XPO:0139827', 'abnormally necrotic foregut', 0.4090909090909091, 5.725717590856133, 1.5304701939081158, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(54072, 'HP:0011131', 'Perianal dermatitis', 'XPO:0100890', 'abnormal pharyngeal cavity', 0.4838709677419355, 5.05060299610679, 1.5632786569919361, 'HP:0025031', 'Abnormality of the digestive system'),
(54073, 'HP:0011131', 'Perianal dermatitis', 'XPO:0102125', 'abnormal liver and biliary system morphology', 0.47368421052631576, 5.725717590856133, 1.6468703703453182, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(54074, 'HP:0011131', 'Perianal dermatitis', 'XPO:0140425', 'abnormally necrotic oral evagination', 0.4186046511627907, 5.725717590856133, 1.5481640787645816, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(54075, 'HP:0011131', 'Perianal dermatitis', 'XPO:0115495', 'abnormally protruding proctodeum', 0.40540540540540543, 5.05060299610679, 1.4309233924911664, 'HP:0025031', 'Abnormality of the digestive system'),
(54076, 'HP:0011131', 'Perianal dermatitis', 'XPO:0102653', 'abnormal dorsal foregut morphology', 0.43902439024390244, 5.725717590856133, 1.5854745895265556, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(54077, 'HP:0011131', 'Perianal dermatitis', 'XPO:0100986', 'abnormal gut epithelium', 0.45454545454545453, 5.05060299610679, 1.5151662069205463, 'HP:0025031', 'Abnormality of the digestive system'),
(54078, 'HP:0011131', 'Perianal dermatitis', 'XPO:0102155', 'abnormal midgut morphology', 0.45, 5.725717590856133, 1.6051706812315194, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(54079, 'HP:0011131', 'Perianal dermatitis', 'XPO:0103711', 'increased size of the alimentary system', 0.4186046511627907, 5.725717590856133, 1.5481640787645816, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(54080, 'HP:0011131', 'Perianal dermatitis', 'XPO:0103321', 'decreased size of the alimentary system', 0.4186046511627907, 5.725717590856133, 1.5481640787645816, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(54081, 'HP:0011131', 'Perianal dermatitis', 'XPO:0101788', 'abnormal foregut morphology', 0.45, 5.725717590856133, 1.6051706812315194, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(54082, 'HP:0011131', 'Perianal dermatitis', 'XPO:0129821', 'increased size of the pharyngeal cavity', 0.43902439024390244, 5.725717590856133, 1.5854745895265556, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(54083, 'HP:0011131', 'Perianal dermatitis', 'XPO:0100493', 'abnormal liver and biliary system', 0.5, 5.05060299610679, 1.5891197242666757, 'HP:0025031', 'Abnormality of the digestive system'),
(54084, 'HP:0011131', 'Perianal dermatitis', 'XPO:0100591', 'abnormal pharyngeal arch', 0.40540540540540543, 5.05060299610679, 1.4309233924911664, 'HP:0025031', 'Abnormality of the digestive system'),
(54085, 'HP:0011131', 'Perianal dermatitis', 'XPO:0142054', 'abnormal digestive tract', 0.4838709677419355, 5.05060299610679, 1.5632786569919361, 'HP:0025031', 'Abnormality of the digestive system'),
(54086, 'HP:0011131', 'Perianal dermatitis', 'XPO:0133432', 'abnormal cilium morphology in the alimentary system', 0.42857142857142855, 5.725717590856133, 1.5664861849086864, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(54087, 'HP:0011131', 'Perianal dermatitis', 'XPO:0103009', 'abnormal manicotto glandulare morphology', 0.46153846153846156, 5.725717590856133, 1.6256195397716668, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(54088, 'HP:0011131', 'Perianal dermatitis', 'XPO:0101101', 'abnormal posterior foregut', 0.45454545454545453, 5.05060299610679, 1.5151662069205463, 'HP:0025031', 'Abnormality of the digestive system'),
(54089, 'HP:0011131', 'Perianal dermatitis', 'XPO:0101784', 'abnormal alimentary system morphology', 0.5, 5.725717590856133, 1.6919984620052309, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(54090, 'HP:0011131', 'Perianal dermatitis', 'XPO:0102367', 'abnormal hindgut morphology', 0.45, 5.725717590856133, 1.6051706812315194, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(54091, 'HP:0011131', 'Perianal dermatitis', 'XPO:0100214', 'abnormal second pancreatic bud', 0.4166666666666667, 5.05060299610679, 1.45066119926208, 'HP:0025031', 'Abnormality of the digestive system'),
(54092, 'HP:0011131', 'Perianal dermatitis', 'XPO:0107304', 'abnormal hindgut endoderm', 0.42857142857142855, 5.05060299610679, 1.471238981671103, 'HP:0025031', 'Abnormality of the digestive system'),
(54093, 'HP:0011131', 'Perianal dermatitis', 'XPO:0107307', 'abnormal posterior hindgut endoderm', 0.4166666666666667, 5.05060299610679, 1.45066119926208, 'HP:0025031', 'Abnormality of the digestive system'),
(54094, 'HP:0011131', 'Perianal dermatitis', 'XPO:0141717', 'abnormal tracheoesophageal fold', 0.4166666666666667, 5.05060299610679, 1.45066119926208, 'HP:0025031', 'Abnormality of the digestive system'),
(54095, 'HP:0011131', 'Perianal dermatitis', 'XPO:0101601', 'abnormal proctodeum', 0.4411764705882353, 5.05060299610679, 1.4927180591674907, 'HP:0025031', 'Abnormality of the digestive system'),
(54096, 'HP:0011131', 'Perianal dermatitis', 'XPO:0102830', 'abnormal digestive enzyme secreting cell morphology', 0.4186046511627907, 5.725717590856133, 1.5481640787645816, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(54097, 'HP:0011131', 'Perianal dermatitis', 'XPO:0102522', 'abnormal pharyngeal cavity morphology', 0.5, 5.725717590856133, 1.6919984620052309, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(54098, 'HP:0011131', 'Perianal dermatitis', 'XPO:0100156', 'abnormal foregut', 0.46875, 5.05060299610679, 1.5386585568036393, 'HP:0025031', 'Abnormality of the digestive system'),
(54099, 'HP:0011131', 'Perianal dermatitis', 'XPO:0101381', 'abnormal ventral foregut', 0.45454545454545453, 5.05060299610679, 1.5151662069205463, 'HP:0025031', 'Abnormality of the digestive system'),
(54100, 'HP:0011131', 'Perianal dermatitis', 'XPO:0139906', 'abnormally necrotic alimentary system', 0.43902439024390244, 5.725717590856133, 1.5854745895265556, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(54101, 'HP:0011131', 'Perianal dermatitis', 'XPO:0100486', 'abnormal oral evagination', 0.46875, 5.05060299610679, 1.5386585568036393, 'HP:0025031', 'Abnormality of the digestive system'),
(54102, 'HP:0011131', 'Perianal dermatitis', 'XPO:0140165', 'abnormally necrotic midgut', 0.4090909090909091, 5.725717590856133, 1.5304701939081158, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(54103, 'HP:0011131', 'Perianal dermatitis', 'XPO:0107375', 'abnormal larval alimentary system morphology', 0.47368421052631576, 5.725717590856133, 1.6468703703453182, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(54104, 'HP:0011131', 'Perianal dermatitis', 'XPO:0131683', 'abnormal stomach epithelium', 0.40540540540540543, 5.05060299610679, 1.4309233924911664, 'HP:0025031', 'Abnormality of the digestive system'),
(54105, 'HP:0011131', 'Perianal dermatitis', 'XPO:0100216', 'abnormal hepato-pancreatic progenitor cell', 0.40540540540540543, 5.05060299610679, 1.4309233924911664, 'HP:0025031', 'Abnormality of the digestive system'),
(54106, 'HP:0011131', 'Perianal dermatitis', 'XPO:0107288', 'abnormal larval alimentary system', 0.5, 5.05060299610679, 1.5891197242666757, 'HP:0025031', 'Abnormality of the digestive system'),
(54107, 'HP:0011131', 'Perianal dermatitis', 'XPO:0100215', 'abnormal first pancreatic bud', 0.42857142857142855, 5.05060299610679, 1.471238981671103, 'HP:0025031', 'Abnormality of the digestive system'),
(54108, 'HP:0011131', 'Perianal dermatitis', 'XPO:0100735', 'abnormal hindgut', 0.46875, 5.05060299610679, 1.5386585568036393, 'HP:0025031', 'Abnormality of the digestive system'),
(54109, 'HP:0011131', 'Perianal dermatitis', 'XPO:0101377', 'abnormal manicotto glandulare', 0.46875, 5.05060299610679, 1.5386585568036393, 'HP:0025031', 'Abnormality of the digestive system'),
(54110, 'HP:0011131', 'Perianal dermatitis', 'XPO:0101847', 'abnormal first pancreatic bud morphology', 0.4090909090909091, 5.725717590856133, 1.5304701939081158, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(54111, 'HP:0011131', 'Perianal dermatitis', 'XPO:0101021', 'abnormal dorsal foregut', 0.45454545454545453, 5.05060299610679, 1.5151662069205463, 'HP:0025031', 'Abnormality of the digestive system'),
(54112, 'HP:0011131', 'Perianal dermatitis', 'XPO:0101198', 'abnormal digestive enzyme secreting cell', 0.42857142857142855, 5.05060299610679, 1.471238981671103, 'HP:0025031', 'Abnormality of the digestive system'),
(54113, 'HP:0011131', 'Perianal dermatitis', 'XPO:0102094', 'abnormal anterior foregut morphology', 0.43902439024390244, 5.725717590856133, 1.5854745895265556, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(54114, 'HP:0011131', 'Perianal dermatitis', 'XPO:0140185', 'abnormally necrotic manicotto glandulare', 0.4090909090909091, 5.725717590856133, 1.5304701939081158, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(54115, 'HP:0011131', 'Perianal dermatitis', 'XPO:0128341', 'decreased size of the pharyngeal cavity', 0.43902439024390244, 5.725717590856133, 1.5854745895265556, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(54116, 'HP:0011131', 'Perianal dermatitis', 'XPO:0140201', 'abnormally necrotic hindgut', 0.4090909090909091, 5.725717590856133, 1.5304701939081158, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(54117, 'HP:0011131', 'Perianal dermatitis', 'XPO:0102618', 'abnormal gut epithelium morphology', 0.43902439024390244, 5.725717590856133, 1.5854745895265556, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(54118, 'HP:0011131', 'Perianal dermatitis', 'XPO:0107306', 'abnormal ventral posterior hindgut endoderm', 0.40540540540540543, 5.05060299610679, 1.4309233924911664, 'HP:0025031', 'Abnormality of the digestive system'),
(54119, 'HP:0011131', 'Perianal dermatitis', 'XPO:0131662', 'abnormal foregut epithelium', 0.40540540540540543, 5.05060299610679, 1.4309233924911664, 'HP:0025031', 'Abnormality of the digestive system'),
(54120, 'HP:0011131', 'Perianal dermatitis', 'XPO:0100523', 'abnormal midgut', 0.46875, 5.05060299610679, 1.5386585568036393, 'HP:0025031', 'Abnormality of the digestive system'),
(54121, 'HP:0011131', 'Perianal dermatitis', 'XPO:0107305', 'abnormal dorsal posterior hindgut endoderm', 0.40540540540540543, 5.05060299610679, 1.4309233924911664, 'HP:0025031', 'Abnormality of the digestive system'),
(54122, 'HP:0011131', 'Perianal dermatitis', 'XPO:0107308', 'abnormal anterior hindgut endoderm', 0.4166666666666667, 5.05060299610679, 1.45066119926208, 'HP:0025031', 'Abnormality of the digestive system'),
(54123, 'HP:0011131', 'Perianal dermatitis', 'XPO:0100130', 'abnormal mouth primordium', 0.40540540540540543, 5.05060299610679, 1.4309233924911664, 'HP:0025031', 'Abnormality of the digestive system'),
(54124, 'HP:0011131', 'Perianal dermatitis', 'XPO:0100492', 'abnormal gall bladder primordium', 0.42857142857142855, 5.05060299610679, 1.471238981671103, 'HP:0025031', 'Abnormality of the digestive system'),
(54125, 'HP:0011131', 'Perianal dermatitis', 'XPO:0100621', 'abnormal peritoneum', 0.42857142857142855, 5.05060299610679, 1.471238981671103, 'HP:0025031', 'Abnormality of the digestive system'),
(54126, 'HP:0011131', 'Perianal dermatitis', 'XPO:0102801', 'abnormal hepato-pancreatic duct morphology', 0.4186046511627907, 5.725717590856133, 1.5481640787645816, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(54127, 'HP:0011131', 'Perianal dermatitis', 'XPO:0142034', 'abnormally necrotic digestive tract', 0.4186046511627907, 5.725717590856133, 1.5481640787645816, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(54128, 'HP:0011131', 'Perianal dermatitis', 'XPO:0115392', 'abnormally incomplete structure of alimentary system', 0.4864864864864865, 5.725717590856133, 1.668977002055292, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(54129, 'HP:0011131', 'Perianal dermatitis', 'XPO:0100152', 'abnormal alimentary system', 0.5172413793103449, 5.05060299610679, 1.6162861318637973, 'HP:0025031', 'Abnormality of the digestive system'),
(54130, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0102520', 'abnormal microtubule morphology', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(54131, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0101079', 'abnormal blastomere D1.1.2', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(54132, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100332', 'abnormal germinal granule', 0.48148148148148145, 3.6715585125471644, 1.3295816755533123, 'UPHENO:0086172', 'abnormal cell'),
(54133, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0101016', 'abnormal egg', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(54134, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0101497', 'abnormal ciliary axoneme', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(54135, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100009', 'abnormal multi-tissue structure', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(54136, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0107272', 'abnormal axial region', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(54137, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0107269', 'abnormal right side', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(54138, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100025', 'abnormal oocyte', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(54139, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0126600', 'abnormally localised progenitor cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(54140, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0126495', 'abnormally localised keratin accumulating cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(54141, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0102636', 'abnormal acid secreting cell morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(54142, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0101278', 'abnormal pigment cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(54143, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0139717', 'abnormally necrotic cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(54144, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100120', 'abnormal genital system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(54145, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0131283', 'abnormally decreased number of myoblast', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(54146, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100232', 'abnormal lymphatic system', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(54147, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0138715', 'decreased cell population proliferation in anatomical cluster', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(54148, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0107271', 'abnormal apical region', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(54149, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0125779', 'absent endoplasmic reticulum', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(54150, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0107262', 'abnormal left-right axis', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(54151, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0101570', 'abnormal forelimb region', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(54152, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0124884', 'absent keratin accumulating cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(54153, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0107284', 'abnormal migrating myoblast', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(54154, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0101168', 'abnormal circulating cell', 0.52, 3.6715585125471644, 1.3817418089225373, 'UPHENO:0086172', 'abnormal cell'),
(54155, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0103099', 'abnormal alkali secreting cell morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(54156, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0101515', 'abnormal neuromast mantle cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(54157, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100274', 'abnormal sensory system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(54158, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0141892', 'abnormal inositol metabolic process', 0.44, 4.758907843651163, 1.447038165082909, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(54159, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0107273', 'abnormal basal region', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(54160, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0102994', 'abnormal vegetal cortex morphology', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(54161, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0101141', 'abnormal Keller explant', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(54162, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100397', 'abnormal ventral vegetal hemisphere blastomere', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(54163, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0131061', 'abnormally increased number of keratin accumulating cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(54164, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100802', 'abnormal exocrine cell', 0.6190476190476191, 3.6715585125471644, 1.5076039119696991, 'UPHENO:0086172', 'abnormal cell'),
(54165, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100999', 'abnormal serous membrane', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(54166, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0102588', 'abnormal centrosome morphology', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(54167, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100587', 'abnormal vestibuloauditory system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(54168, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0135479', 'increased cell population proliferation in male organism', 0.4166666666666667, 5.835653092541957, 1.5593338712067029, 'HP:0011017', 'Abnormal cellular physiology'),
(54169, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0141788', 'abnormal hormone biosynthetic process', 0.4074074074074074, 4.758907843651163, 1.392413123563799, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(54170, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0127979', 'abnormally localised absorptive cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(54171, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100899', 'abnormal secondary spermatogonium', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(54172, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0131180', 'abnormally decreased number of cell', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(54173, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0126133', 'absent mitotic cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(54174, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0131513', 'absent actin cytoskeleton', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(54175, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100003', 'abnormal organism subdivision', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(54176, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100004', 'abnormal cell', 0.65, 3.6715585125471644, 1.5448343060521594, 'UPHENO:0086172', 'abnormal cell'),
(54177, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0131346', 'abnormally decreased number of chondroblast', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(54178, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0101347', 'abnormal hindlimb region', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(54179, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0139623', 'decreased cell population proliferation in ventral region', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(54180, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100251', 'abnormal proteinaceous extracellular matrix', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(54181, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0131136', 'abnormally increased number of multiciliated cell precursor', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(54182, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0138844', 'decreased cell population proliferation in extracellular matrix', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(54183, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100151', 'abnormal primordium', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(54184, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0102534', 'abnormal spermatocyte morphology', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(54185, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0125533', 'absent myelin accumulating cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(54186, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0141498', 'abnormal axon microtubule bundle', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(54187, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0126630', 'abnormally localised early embryonic cell', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(54188, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0126697', 'abnormally localised proepicardium', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(54189, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0102024', 'abnormal cilium morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(54190, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100218', 'abnormal epithelial cell', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(54191, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0124984', 'absent progenitor cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(54192, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100960', 'abnormal postmigratory neural crest cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(54193, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0102423', 'abnormal multiciliated cell precursor morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(54194, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0141784', 'abnormal cellular hormone metabolic process', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(54195, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0138738', 'decreased cell population proliferation in anatomical region', 0.4166666666666667, 5.835653092541957, 1.5593338712067029, 'HP:0011017', 'Abnormal cellular physiology'),
(54196, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0101374', 'abnormal migratory neural crest cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(54197, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0131691', 'abnormal molecular function', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(54198, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0126413', 'abnormally localised cell part', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(54199, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100172', 'abnormal stem cell', 0.6190476190476191, 3.6715585125471644, 1.5076039119696991, 'UPHENO:0086172', 'abnormal cell'),
(54200, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0138820', 'decreased cell population proliferation in anatomical line', 0.4411764705882353, 5.835653092541957, 1.6045413160604438, 'HP:0011017', 'Abnormal cellular physiology'),
(54201, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100596', 'abnormal myocyte', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(54202, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0127160', 'abnormally localised acid secreting cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(54203, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0101518', 'abnormal B cell', 0.48148148148148145, 3.6715585125471644, 1.3295816755533123, 'UPHENO:0086172', 'abnormal cell'),
(54204, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100344', 'abnormal portion of organism substance', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(54205, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100108', 'abnormal cell part', 0.6190476190476191, 3.6715585125471644, 1.5076039119696991, 'UPHENO:0086172', 'abnormal cell'),
(54206, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0135160', 'increased cell population proliferation in embryo', 0.4166666666666667, 5.835653092541957, 1.5593338712067029, 'HP:0011017', 'Abnormal cellular physiology'),
(54207, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0101389', 'abnormal wedge region', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(54208, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0101500', 'abnormal endodermal cell', 0.48148148148148145, 3.6715585125471644, 1.3295816755533123, 'UPHENO:0086172', 'abnormal cell'),
(54209, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0138578', 'decreased cell population proliferation in anatomical system', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(54210, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0139626', 'decreased cell population proliferation in antero-ventral region', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(54211, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0101406', 'abnormal cleavage furrow', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(54212, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0125854', 'absent barrier epithelial cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(54213, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0107286', 'abnormal efferent neuron', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(54214, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0102347', 'abnormal ciliated cell morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(54215, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0141738', 'abnormal carbon dioxide homeostasis', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(54216, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0131354', 'abnormally decreased number of multiciliated cell precursor', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(54217, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0101072', 'abnormal mitochondrial cloud', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(54218, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0102764', 'abnormal apoptotic cell morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(54219, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0131669', 'abnormal Roux spot', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(54220, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0103080', 'abnormal myelin accumulating cell morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(54221, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100702', 'abnormal glial cell', 0.5, 3.6715585125471644, 1.3549093166236559, 'UPHENO:0086172', 'abnormal cell'),
(54222, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0125115', 'absent paracrine cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(54223, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0138576', 'decreased cell population proliferation in anatomical structure', 0.4411764705882353, 5.835653092541957, 1.6045413160604438, 'HP:0011017', 'Abnormal cellular physiology'),
(54224, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100308', 'abnormal early embryonic cell', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(54225, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0101535', 'abnormal absorptive cell', 0.6190476190476191, 3.6715585125471644, 1.5076039119696991, 'UPHENO:0086172', 'abnormal cell'),
(54226, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0139619', 'decreased cell population proliferation in basal region', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(54227, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0138609', 'decreased cell population proliferation in tissue', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(54228, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100335', 'abnormal commissural interneuron', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(54229, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100035', 'abnormal ventral animal hemisphere blastomere', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(54230, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0115509', 'abnormally semi-viable whole organism', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(54231, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0102356', 'abnormal kinetochore morphology', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(54232, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100862', 'abnormal blastomere V1', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(54233, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0102704', 'abnormal mitochondrial cloud morphology', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(54234, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0142030', 'abnormally localised desmosome', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(54235, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0131308', 'abnormally decreased number of oxygen accumulating cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(54236, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0131550', 'abnormally localised adherens junction', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(54237, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0125824', 'absent nucleus', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(54238, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0138580', 'decreased cell population proliferation in female organism', 0.4166666666666667, 5.835653092541957, 1.5593338712067029, 'HP:0011017', 'Abnormal cellular physiology'),
(54239, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0133436', 'abnormal cilium morphology in the multiciliated cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(54240, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0101504', 'abnormal blastomere D2.2.1', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(54241, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0101921', 'abnormal chondroblast morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(54242, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100653', 'abnormal myoblast', 0.6190476190476191, 3.6715585125471644, 1.5076039119696991, 'UPHENO:0086172', 'abnormal cell'),
(54243, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0102386', 'abnormal electrically active cell morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(54244, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100864', 'abnormal dorsolateral ascending neuron', 0.48148148148148145, 3.6715585125471644, 1.3295816755533123, 'UPHENO:0086172', 'abnormal cell'),
(54245, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100164', 'abnormal neural nucleus', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(54246, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0124807', 'absent cell part', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(54247, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0101023', 'abnormal ultimobranchial body', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(54248, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0102958', 'abnormal cementoblast morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(54249, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100520', 'abnormal blastomere D1.2', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(54250, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100192', 'abnormal epithelium', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(54251, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0102531', 'abnormal secondary spermatogonium morphology', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(54252, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0101333', 'abnormal barrier epithelial cell', 0.6190476190476191, 3.6715585125471644, 1.5076039119696991, 'UPHENO:0086172', 'abnormal cell'),
(54253, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0131667', 'abnormal actin cytoskeleton', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(54254, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0102852', 'abnormal centriole morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(54255, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100392', 'abnormal cilium', 0.5652173913043478, 3.6715585125471644, 1.440565418328227, 'UPHENO:0086172', 'abnormal cell'),
(54256, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0139580', 'decreased cell population proliferation in thoracic region', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(54257, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0141841', 'abnormality of whole organism mass', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(54258, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0126982', 'abnormally localised secondary oogonium', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(54259, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0126318', 'abnormally localised cell', 0.48148148148148145, 3.6715585125471644, 1.3295816755533123, 'UPHENO:0086172', 'abnormal cell'),
(54260, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0101192', 'abnormal blastomere D2.1', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(54261, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0131720', 'abnormal mitotic spindle assembly', 0.45454545454545453, 5.835653092541957, 1.6286711109119212, 'HP:0011017', 'Abnormal cellular physiology'),
(54262, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100887', 'abnormal right-dorsal blastomere', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(54263, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0101187', 'abnormal dorsolateral commissural neuron', 0.48148148148148145, 3.6715585125471644, 1.3295816755533123, 'UPHENO:0086172', 'abnormal cell'),
(54264, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0136518', 'increased cell population proliferation in anterior region', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(54265, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100640', 'abnormal notochordal sheath', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(54266, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0102860', 'abnormal mesenchymal stem cell morphology', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(54267, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100721', 'abnormal centromere', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(54268, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0124716', 'absent cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(54269, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0127217', 'abnormally localised cilium', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(54270, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0127399', 'abnormally localised melanoblast', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(54271, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0101534', 'abnormal blastomere V2.1.1', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(54272, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0103644', 'abnormally decreased number of cilium in the multiciliated cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(54273, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0107324', 'abnormal embryonic thrombocyte', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(54274, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100715', 'abnormal ciliated cell', 0.6190476190476191, 3.6715585125471644, 1.5076039119696991, 'UPHENO:0086172', 'abnormal cell'),
(54275, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100745', 'abnormal anterior lymph sac', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(54276, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0141798', 'abnormal lipid metabolic process', 0.44, 4.758907843651163, 1.447038165082909, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(54277, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0131171', 'abnormally increased number of barrier epithelial cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(54278, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0138232', 'decreased cell population proliferation in forelimb region', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(54279, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100477', 'abnormal pericyte', 0.6190476190476191, 3.6715585125471644, 1.5076039119696991, 'UPHENO:0086172', 'abnormal cell'),
(54280, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0141796', 'abnormal demethylation', 0.4782608695652174, 4.758907843651163, 1.508641575552437, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(54281, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100859', 'abnormal blastomere V1.1.2', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(54282, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0101658', 'abnormal germ cell morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(54283, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0138822', 'decreased cell population proliferation in extraembryonic structure', 0.4166666666666667, 5.835653092541957, 1.5593338712067029, 'HP:0011017', 'Abnormal cellular physiology'),
(54284, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100667', 'abnormal vegetal yolk mass', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(54285, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0141289', 'abnormal spindle microtubule morphology', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(54286, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0107312', 'abnormal filopodium', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(54287, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0135736', 'increased cell population proliferation in cell condensation', 0.4166666666666667, 5.835653092541957, 1.5593338712067029, 'HP:0011017', 'Abnormal cellular physiology'),
(54288, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0125454', 'absent myoblast', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(54289, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0126671', 'abnormally localised zygote', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(54290, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0142064', 'abnormal desmosome morphology', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(54291, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0126473', 'abnormally localised germ cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(54292, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0135475', 'increased cell population proliferation in anatomical group', 0.4166666666666667, 5.835653092541957, 1.5593338712067029, 'HP:0011017', 'Abnormal cellular physiology'),
(54293, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100317', 'abnormal respiratory system', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(54294, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100216', 'abnormal hepato-pancreatic progenitor cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(54295, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0103041', 'abnormal perivitelline space morphology', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(54296, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0131666', 'abnormal adherens junction', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(54297, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0135788', 'increased cell population proliferation in intersomitic region', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(54298, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0103642', 'increased cell population proliferation', 0.5172413793103449, 5.835653092541957, 1.7373661832679608, 'HP:0011017', 'Abnormal cellular physiology'),
(54299, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100481', 'abnormal anatomical line', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(54300, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0127819', 'abnormally localised ciliary axoneme', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(54301, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100991', 'abnormal iliac process primordium', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(54302, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0131347', 'abnormally decreased number of myelin accumulating cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(54303, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100415', 'abnormal secretory epithelial cell', 0.52, 3.6715585125471644, 1.3817418089225373, 'UPHENO:0086172', 'abnormal cell'),
(54304, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0135474', 'increased cell population proliferation in anatomical structure', 0.4411764705882353, 5.835653092541957, 1.6045413160604438, 'HP:0011017', 'Abnormal cellular physiology'),
(54305, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0107303', 'abnormal migratory trunk neural crest cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(54306, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0101283', 'abnormal left-ventral blastomere', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(54307, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100239', 'abnormal acellular anatomical structure', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(54308, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0135477', 'increased cell population proliferation in whole organism', 0.42857142857142855, 5.835653092541957, 1.5814531869511603, 'HP:0011017', 'Abnormal cellular physiology'),
(54309, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0131089', 'abnormally increased number of mitotic cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(54310, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100742', 'abnormal musculoskeletal system', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(54311, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0101176', 'abnormal non-ciliated epithelial cell', 0.52, 3.6715585125471644, 1.3817418089225373, 'UPHENO:0086172', 'abnormal cell'),
(54312, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100557', 'abnormal prime meridian', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(54313, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0138584', 'decreased cell population proliferation in cell', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(54314, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0141794', 'abnormal prosthetic group metabolic process', 0.4782608695652174, 4.758907843651163, 1.508641575552437, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(54315, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0101345', 'abnormal ascending interneuron', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(54316, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0101466', 'abnormal secondary myofiber', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(54317, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0133473', 'abnormally decreased number of cilium in the ciliated non-epidermal cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(54318, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0103129', 'abnormal ciliary axoneme morphology', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(54319, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100014', 'abnormal tissue', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(54320, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0101494', 'abnormal blastomere D1.2.1', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(54321, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100762', 'abnormal intersomitic region', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(54322, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0141789', 'abnormal hormone catabolic process', 0.4074074074074074, 4.758907843651163, 1.392413123563799, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(54323, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0115512', 'abnormally semi-erect whole organism', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(54324, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0124934', 'absent centrosome', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(54325, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100900', 'abnormal angioblast', 0.52, 3.6715585125471644, 1.3817418089225373, 'UPHENO:0086172', 'abnormal cell'),
(54326, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0115505', 'dead whole organism', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(54327, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100888', 'abnormal microtubule', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(54328, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0138262', 'decreased cell population proliferation in embryo', 0.4166666666666667, 5.835653092541957, 1.5593338712067029, 'HP:0011017', 'Abnormal cellular physiology'),
(54329, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0141497', 'abnormal lymphoblast', 0.5, 3.6715585125471644, 1.3549093166236559, 'UPHENO:0086172', 'abnormal cell'),
(54330, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0127522', 'abnormally localised cementoblast', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(54331, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0127821', 'abnormally localised apoptotic cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(54332, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0141772', 'abnormal water homeostasis', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(54333, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0101212', 'abnormal glomeral mesenchyme', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(54334, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0131348', 'abnormally decreased number of absorptive cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(54335, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100852', 'abnormal interdigital region', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(54336, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0125785', 'absent mitotic spindle', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(54337, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0101463', 'abnormal right-ventral blastomere', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(54338, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100186', 'abnormal uveal tract', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(54339, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0102896', 'abnormal mitotic spindle morphology', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(54340, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0131735', 'abnormal spindle assembly', 0.5172413793103449, 5.835653092541957, 1.7373661832679608, 'HP:0011017', 'Abnormal cellular physiology'),
(54341, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0102965', 'abnormal barrier epithelial cell morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(54342, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0141786', 'abnormal pigment metabolic process', 0.4782608695652174, 4.758907843651163, 1.508641575552437, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(54343, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0101241', 'abnormal nucleate erythrocyte', 0.6190476190476191, 3.6715585125471644, 1.5076039119696991, 'UPHENO:0086172', 'abnormal cell'),
(54344, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0131129', 'abnormally increased number of chondroblast', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(54345, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0103104', 'abnormal zygote cortex morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(54346, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0101157', 'abnormal female organism', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(54347, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100114', 'abnormal peripheral nervous system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(54348, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0141421', 'decreased cell population proliferation in tadpole', 0.4166666666666667, 5.835653092541957, 1.5593338712067029, 'HP:0011017', 'Abnormal cellular physiology'),
(54349, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0127372', 'abnormally localised polar body', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(54350, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0101220', 'abnormal centriole', 0.5652173913043478, 3.6715585125471644, 1.440565418328227, 'UPHENO:0086172', 'abnormal cell'),
(54351, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0107339', 'abnormal yolk platelet', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(54352, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100976', 'abnormal multiciliated cell', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(54353, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0107265', 'abnormal posterior side', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(54354, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100060', 'abnormal regenerating tissue', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(54355, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0141797', 'abnormal hydrogen metabolic process', 0.4782608695652174, 4.758907843651163, 1.508641575552437, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(54356, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100268', 'abnormal circulatory system', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(54357, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0131314', 'abnormally decreased number of exocrine cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(54358, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0131131', 'abnormally increased number of absorptive cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(54359, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0101158', 'abnormal blastomere V2.2.2', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(54360, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0130986', 'abnormally increased number of germ cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(54361, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100023', 'abnormal mesenchyme', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(54362, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0103179', 'abnormal lampbrush chromosome morphology', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(54363, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0138606', 'decreased cell population proliferation in multi-tissue structure', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(54364, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100551', 'abnormal oocyte cortex', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(54365, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0131082', 'abnormally increased number of alkali secreting cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(54366, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100733', 'abnormal fibroblast', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(54367, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0136478', 'increased cell population proliferation in thoracic region', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(54368, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0125394', 'absent multiciliated cell precursor', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(54369, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0127743', 'abnormally localised perivitelline space', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(54370, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100429', 'abnormal spermatid', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(54371, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0126983', 'abnormally localised primordial germ cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(54372, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100152', 'abnormal alimentary system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(54373, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0142051', 'abnormal cerebrospinal fluid', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(54374, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0136567', 'increased cell population proliferation in ventro-lateral region', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(54375, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100189', 'abnormal enteroendocrine cell', 0.48148148148148145, 3.6715585125471644, 1.3295816755533123, 'UPHENO:0086172', 'abnormal cell'),
(54376, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0107253', 'abnormal enteric nervous system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(54377, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0136525', 'increased cell population proliferation in postero-dorsal region', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(54378, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0139628', 'decreased cell population proliferation in postero-ventral region', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(54379, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0127815', 'abnormally localised ciliated non-epidermal cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(54380, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0136398', 'increased cell population proliferation in egg jelly', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(54381, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0131292', 'abnormally decreased number of mucus secreting cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(54382, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0127520', 'abnormally localised gastrula cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(54383, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0101452', 'abnormal blastomere V1.1.1', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(54384, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100509', 'abnormal germ plasm', 0.5, 3.6715585125471644, 1.3549093166236559, 'UPHENO:0086172', 'abnormal cell'),
(54385, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0101325', 'abnormal blastomere D2.1.1', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(54386, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0102873', 'abnormal nucleate erythrocyte morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(54387, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0101237', 'abnormal mucus secreting cell', 0.6190476190476191, 3.6715585125471644, 1.5076039119696991, 'UPHENO:0086172', 'abnormal cell'),
(54388, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100807', 'abnormal matrix-based tissue', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(54389, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0131708', 'abnormal cilium disassembly', 0.5555555555555556, 5.835653092541957, 1.8005636605953823, 'HP:0011017', 'Abnormal cellular physiology'),
(54390, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0101264', 'abnormal mitotic spindle', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(54391, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100225', 'abnormal endocrine system', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(54392, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0141790', 'abnormal cellular metabolic process', 0.4583333333333333, 4.758907843651163, 1.4768771428276568, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(54393, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0136321', 'increased cell population proliferation in multicellular anatomical structure', 0.4166666666666667, 5.835653092541957, 1.5593338712067029, 'HP:0011017', 'Abnormal cellular physiology'),
(54394, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0127824', 'abnormally localised alkali secreting cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(54395, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100649', 'abnormal growth cone', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(54396, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0141770', 'abnormal urate homeostasis', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(54397, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0139423', 'decreased cell population proliferation in multicellular anatomical structure', 0.4166666666666667, 5.835653092541957, 1.5593338712067029, 'HP:0011017', 'Abnormal cellular physiology'),
(54398, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100954', 'abnormal neural progenitor cell', 0.48148148148148145, 3.6715585125471644, 1.3295816755533123, 'UPHENO:0086172', 'abnormal cell'),
(54399, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0135716', 'increased cell population proliferation in portion of organism substance', 0.4411764705882353, 5.835653092541957, 1.6045413160604438, 'HP:0011017', 'Abnormal cellular physiology'),
(54400, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100176', 'abnormal stage VI oocyte', 0.5652173913043478, 3.6715585125471644, 1.440565418328227, 'UPHENO:0086172', 'abnormal cell'),
(54401, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100511', 'abnormal stylopod', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(54402, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0138717', 'decreased cell population proliferation in acellular anatomical structure', 0.4166666666666667, 5.835653092541957, 1.5593338712067029, 'HP:0011017', 'Abnormal cellular physiology'),
(54403, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0131725', 'abnormal phosphorylation of RNA polymerase II C-terminal domain', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(54404, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0101327', 'abnormal blastomere V1.2.1', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(54405, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:00000000', 'Xenopus phenotype', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(54406, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0127363', 'abnormally localised barrier cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(54407, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100724', 'abnormal kinetochore', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(54408, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0133443', 'abnormally increased number of cilium in the multiciliated cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(54409, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0139293', 'decreased cell population proliferation in organ part', 0.42857142857142855, 5.835653092541957, 1.5814531869511603, 'HP:0011017', 'Abnormal cellular physiology'),
(54410, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0130973', 'abnormally increased number of stem cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(54411, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0138585', 'decreased cell population proliferation in organism subdivision', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(54412, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0101109', 'abnormal egg cell-free extract', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(54413, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100674', 'abnormal secondary oogonium', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(54414, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0101917', 'abnormal progenitor cell morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(54415, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0135131', 'increased cell population proliferation in hindlimb region', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(54416, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100384', 'abnormal amputated tissue', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(54417, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0115391', 'abnormally undifferentiated alimentary system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(54418, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0107325', 'abnormal adult thrombocyte', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(54419, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0101302', 'abnormal subcortical cytoplasm', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(54420, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0102147', 'abnormal somatic stem cell morphology', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(54421, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0135613', 'increased cell population proliferation in anatomical cluster', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(54422, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0136517', 'increased cell population proliferation in basal region', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(54423, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0141791', 'abnormal primary metabolic process', 0.4782608695652174, 4.758907843651163, 1.508641575552437, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(54424, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0141511', 'abnormally localised nucleus in myoblast', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(54425, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100856', 'abnormal simple organ', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(54426, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0142066', 'abnormally increased number of desmosome', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(54427, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0135482', 'increased cell population proliferation in cell', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(54428, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0107268', 'abnormal left side', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(54429, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0115615', 'abnormally posteriorly mislocalised primordial germ cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(54430, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0102061', 'abnormal spermatid morphology', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(54431, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0101472', 'abnormal zygote cortex', 0.5652173913043478, 3.6715585125471644, 1.440565418328227, 'UPHENO:0086172', 'abnormal cell'),
(54432, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0101096', 'abnormal tendon', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(54433, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100521', 'abnormal animal blastomere', 0.48148148148148145, 3.6715585125471644, 1.3295816755533123, 'UPHENO:0086172', 'abnormal cell'),
(54434, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0101078', 'abnormal mucous gland', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(54435, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0125644', 'absent pericyte', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(54436, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0131307', 'abnormally decreased number of mitotic cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(54437, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0101174', 'abnormal articular system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(54438, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100872', 'abnormal neuroendocrine cell', 0.48148148148148145, 3.6715585125471644, 1.3295816755533123, 'UPHENO:0086172', 'abnormal cell'),
(54439, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0101037', 'abnormal hatching gland cell', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(54440, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0141715', 'abnormal septum', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(54441, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0131512', 'absent adherens junction', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(54442, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100503', 'abnormal blastomere D2', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(54443, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0101132', 'abnormal apoptotic cell', 0.6190476190476191, 3.6715585125471644, 1.5076039119696991, 'UPHENO:0086172', 'abnormal cell'),
(54444, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0131165', 'abnormally increased number of cementoblast', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(54445, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100704', 'abnormal Merkel cell', 0.6190476190476191, 3.6715585125471644, 1.5076039119696991, 'UPHENO:0086172', 'abnormal cell'),
(54446, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0135504', 'increased cell population proliferation in multi-tissue structure', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(54447, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0101461', 'abnormal sperm entry point', 0.5652173913043478, 3.6715585125471644, 1.440565418328227, 'UPHENO:0086172', 'abnormal cell'),
(54448, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0127703', 'abnormally localised morula cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(54449, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100422', 'abnormal notochord', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(54450, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100395', 'abnormal blastomere D1.1', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(54451, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0131075', 'abnormally increased number of mucus secreting cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(54452, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0101448', 'abnormal myelin accumulating cell', 0.6190476190476191, 3.6715585125471644, 1.5076039119696991, 'UPHENO:0086172', 'abnormal cell'),
(54453, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0141314', 'abnormal Roux spot morphology', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(54454, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0115758', 'abnormally decreased mobility of melanoblast', 0.52, 3.6715585125471644, 1.3817418089225373, 'UPHENO:0086172', 'abnormal cell'),
(54455, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0127508', 'abnormally localised barrier epithelial cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(54456, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0138233', 'decreased cell population proliferation in hindlimb region', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(54457, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0101451', 'abnormal dorsal lymph space', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(54458, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0101575', 'abnormal vitelline membrane', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(54459, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0135509', 'increased cell population proliferation in embryonic structure', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(54460, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100465', 'abnormal skeletal system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(54461, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0101657', 'abnormal oocyte morphology', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(54462, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0115508', 'abnormally peramorphic growth of whole organism', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(54463, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0141272', 'absent surface breathing', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(54464, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100894', 'abnormal nucleus', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(54465, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0125868', 'absent cementoblast', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(54466, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0139621', 'decreased cell population proliferation in posterior region', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(54467, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0142067', 'abnormally necrotic desmosome', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(54468, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100728', 'abnormal cell condensation', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(54469, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100642', 'abnormal gustatory system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(54470, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0133445', 'abnormally increased number of cilium in the ciliated non-epidermal cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(54471, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0101435', 'abnormal paracrine cell', 0.6190476190476191, 3.6715585125471644, 1.5076039119696991, 'UPHENO:0086172', 'abnormal cell'),
(54472, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100675', 'abnormal dorsal vegetal hemisphere blastomere', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(54473, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100545', 'abnormal male organism', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(54474, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100676', 'abnormal blastomere D2.2', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(54475, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0141860', 'abnormal malate-aspartate shuttle', 0.4583333333333333, 4.758907843651163, 1.4768771428276568, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(54476, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100533', 'abnormal melanoblast', 0.6190476190476191, 3.6715585125471644, 1.5076039119696991, 'UPHENO:0086172', 'abnormal cell'),
(54477, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0127513', 'abnormally localised nucleate erythrocyte', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(54478, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0131090', 'abnormally increased number of oxygen accumulating cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(54479, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0125013', 'absent early embryonic cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(54480, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100626', 'abnormal primordial germ cell', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(54481, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100336', 'abnormal interneuron', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(54482, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0127337', 'abnormally localised oxygen accumulating cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(54483, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100402', 'abnormal zeugopod', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(54484, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100969', 'abnormal disaggregated/reaggregated ectoderm treated with activin', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(54485, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100006', 'abnormal anatomical structure', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(54486, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0101378', 'abnormal blastomere D1', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(54487, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0102703', 'abnormal endoplasmic reticulum morphology', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(54488, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0125559', 'absent electrically active cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(54489, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0101297', 'abnormal barrier cell', 0.6190476190476191, 3.6715585125471644, 1.5076039119696991, 'UPHENO:0086172', 'abnormal cell'),
(54490, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0136522', 'increased cell population proliferation in medial region', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(54491, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0136519', 'increased cell population proliferation in posterior region', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(54492, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0107399', 'abnormal filopodium morphology', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(54493, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100203', 'abnormal endocrine cell', 0.5, 3.6715585125471644, 1.3549093166236559, 'UPHENO:0086172', 'abnormal cell'),
(54494, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0127171', 'abnormally localised myelin accumulating cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(54495, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0127476', 'abnormally localised nucleus', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(54496, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0127740', 'abnormally localised yolk platelet', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(54497, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0131389', 'abnormally decreased number of barrier epithelial cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(54498, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0101467', 'abnormal alkali secreting cell', 0.6190476190476191, 3.6715585125471644, 1.5076039119696991, 'UPHENO:0086172', 'abnormal cell'),
(54499, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0126454', 'abnormally localised stem cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(54500, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100084', 'abnormal anatomical group', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(54501, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0141907', 'abnormal putrescine metabolic process', 0.44, 4.758907843651163, 1.447038165082909, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(54502, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0101409', 'abnormal perivitelline space', 0.5652173913043478, 3.6715585125471644, 1.440565418328227, 'UPHENO:0086172', 'abnormal cell'),
(54503, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100570', 'abnormal axon', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(54504, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100293', 'abnormal duct', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(54505, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0102258', 'abnormal primordial germ cell morphology', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(54506, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0141745', 'abnormal creatinine homeostasis', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(54507, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100316', 'abnormal gamete', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(54508, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0142052', 'abnormal nasal region', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(54509, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0102929', 'abnormal barrier cell morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(54510, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0103167', 'abnormal absorptive cell morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(54511, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100417', 'abnormal dense regular connective tissue', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(54512, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0135636', 'increased cell population proliferation in anatomical region', 0.4166666666666667, 5.835653092541957, 1.5593338712067029, 'HP:0011017', 'Abnormal cellular physiology'),
(54513, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100175', 'abnormal migrating neuroblast', 0.5, 3.6715585125471644, 1.3549093166236559, 'UPHENO:0086172', 'abnormal cell'),
(54514, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0135130', 'increased cell population proliferation in forelimb region', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(54515, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0116091', 'abnormally increased variability of size of cell in endoderm', 0.48148148148148145, 3.6715585125471644, 1.3295816755533123, 'UPHENO:0086172', 'abnormal cell'),
(54516, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0142023', 'absent desmosome', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(54517, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0107258', 'abnormal anatomical axis', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(54518, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0101636', 'abnormal cell morphology', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(54519, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100010', 'abnormal multicellular anatomical structure', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(54520, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0141778', 'abnormal biosynthetic process', 0.4782608695652174, 4.758907843651163, 1.508641575552437, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(54521, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0141775', 'abnormal nitrogen compound metabolic process', 0.4782608695652174, 4.758907843651163, 1.508641575552437, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(54522, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0126214', 'absent microtubule', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(54523, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0139617', 'decreased cell population proliferation in apical region', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(54524, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0102934', 'abnormal subcortical cytoplasm morphology', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(54525, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0131687', 'abnormal astral microtubule', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(54526, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0101083', 'abnormal T cell', 0.48148148148148145, 3.6715585125471644, 1.3295816755533123, 'UPHENO:0086172', 'abnormal cell'),
(54527, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0141266', 'abnormal surface breathing', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(54528, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0141277', 'abnormal actin cytoskeleton morphology', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(54529, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0125833', 'absent kinetochore', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(54530, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0126725', 'abnormally localised epithelial cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(54531, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100449', 'abnormal lymphocyte', 0.5, 3.6715585125471644, 1.3549093166236559, 'UPHENO:0086172', 'abnormal cell'),
(54532, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0125976', 'absent centriole', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(54533, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0107426', 'abnormal yolk platelet morphology', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(54534, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0102336', 'abnormal Merkel cell morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(54535, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0133441', 'abnormally increased number of cilium in the ciliated cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(54536, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0136028', 'increased cell population proliferation in interdigital region', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(54537, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0124845', 'absent stem cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(54538, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0125698', 'absent filopodium', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(54539, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0127876', 'abnormally localised microtubule', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(54540, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0101940', 'abnormal early embryonic cell morphology', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(54541, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0101366', 'abnormal morula cell', 0.5652173913043478, 3.6715585125471644, 1.440565418328227, 'UPHENO:0086172', 'abnormal cell'),
(54542, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100861', 'abnormal blastomere D2.2.2', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(54543, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0101740', 'abnormal cell part morphology', 0.48148148148148145, 3.6715585125471644, 1.3295816755533123, 'UPHENO:0086172', 'abnormal cell'),
(54544, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0131723', 'abnormal pathway-restricted SMAD protein phosphorylation', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(54545, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0141263', 'abnormal visually guided collision avoidance behavior', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(54546, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0127018', 'abnormally localised ciliated cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(54547, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0141781', 'abnormal secondary metabolic process', 0.4782608695652174, 4.758907843651163, 1.508641575552437, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(54548, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100031', 'abnormal central nervous system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(54549, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0131706', 'abnormal ciliary basal body organization', 0.5555555555555556, 5.835653092541957, 1.8005636605953823, 'HP:0011017', 'Abnormal cellular physiology'),
(54550, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100732', 'abnormal tendon fibroblast', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(54551, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0127683', 'abnormally localised centromere', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(54552, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0101113', 'abnormal stage IV oocyte', 0.5652173913043478, 3.6715585125471644, 1.440565418328227, 'UPHENO:0086172', 'abnormal cell'),
(54553, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0138837', 'decreased cell population proliferation in process', 0.4166666666666667, 5.835653092541957, 1.5593338712067029, 'HP:0011017', 'Abnormal cellular physiology'),
(54554, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0136526', 'increased cell population proliferation in postero-ventral region', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(54555, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100337', 'abnormal zygote', 0.6190476190476191, 3.6715585125471644, 1.5076039119696991, 'UPHENO:0086172', 'abnormal cell'),
(54556, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0125160', 'absent exocrine cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(54557, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0135735', 'increased cell population proliferation in process', 0.4166666666666667, 5.835653092541957, 1.5593338712067029, 'HP:0011017', 'Abnormal cellular physiology'),
(54558, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0131031', 'abnormally increased number of nucleate erythrocyte', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(54559, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0141271', 'increased surface breathing', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(54560, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0101240', 'abnormal ciliated non-epidermal cell', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(54561, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0136191', 'increased cell population proliferation in organ part', 0.42857142857142855, 5.835653092541957, 1.5814531869511603, 'HP:0011017', 'Abnormal cellular physiology'),
(54562, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0102693', 'abnormal plasma membrane morphology', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(54563, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0131352', 'abnormally decreased number of barrier cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(54564, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0125750', 'absent melanoblast', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(54565, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0139624', 'decreased cell population proliferation in medial region', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(54566, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0130988', 'abnormally increased number of pericyte', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(54567, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0142057', 'abnormal desmosome', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(54568, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0135742', 'increased cell population proliferation in extracellular matrix', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(54569, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0101136', 'abnormal ooplasm', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(54570, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100531', 'abnormal proliferative region', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(54571, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0126548', 'abnormally localised centrosome', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(54572, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0130989', 'abnormally increased number of ciliated cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(54573, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0125530', 'absent chondroblast', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(54574, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0138579', 'decreased cell population proliferation in whole organism', 0.42857142857142855, 5.835653092541957, 1.5814531869511603, 'HP:0011017', 'Abnormal cellular physiology'),
(54575, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0107267', 'abnormal ventral side', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(54576, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100688', 'abnormal adipose tissue', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(54577, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0127975', 'abnormally localised mitochondrial cloud', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(54578, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100062', 'abnormal anatomical space', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(54579, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100265', 'abnormal sensory epithelial cell', 0.52, 3.6715585125471644, 1.3817418089225373, 'UPHENO:0086172', 'abnormal cell'),
(54580, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0127339', 'abnormally localised migrating myoblast', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(54581, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100002', 'abnormal head', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(54582, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0136521', 'increased cell population proliferation in ventral region', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(54583, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0127631', 'abnormally localised centriole', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(54584, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0135478', 'increased cell population proliferation in female organism', 0.4166666666666667, 5.835653092541957, 1.5593338712067029, 'HP:0011017', 'Abnormal cellular physiology'),
(54585, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0127653', 'abnormally localised Merkel cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(54586, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0139622', 'decreased cell population proliferation in dorsal region', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(54587, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0101110', 'abnormal cell-free extract', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(54588, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0129551', 'increased size of the cell part', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(54589, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100814', 'abnormal natural killer cell', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(54590, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0136523', 'increased cell population proliferation in antero-dorsal region', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(54591, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0107263', 'abnormal anatomical side', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(54592, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0141777', 'abnormal catabolic process', 0.4782608695652174, 4.758907843651163, 1.508641575552437, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(54593, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100372', 'abnormal hematological system', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(54594, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0139130', 'decreased cell population proliferation in interdigital region', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(54595, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0127428', 'abnormally localised endoplasmic reticulum', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(54596, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0101350', 'abnormal blastomere D2.1.2', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(54597, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100599', 'abnormal adult immune system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(54598, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100104', 'abnormal embryonic structure', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(54599, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100028', 'abnormal anatomical cluster', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(54600, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100231', 'abnormal compound organ', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(54601, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100282', 'abnormal pelvic girdle primordium', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(54602, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0125693', 'absent mucus secreting cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(54603, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0138424', 'decreased cell population proliferation in marginal zone (sensu neural)', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(54604, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0131004', 'abnormally increased number of proepicardium', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(54605, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0101094', 'abnormal blastomere V2.2.1', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(54606, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0103631', 'abnormally increased number of apoptotic cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(54607, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100924', 'abnormal spermatozoon', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(54608, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0102768', 'abnormal ooplasm morphology', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(54609, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0136568', 'increased cell population proliferation in dorso-lateral region', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(54610, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0101519', 'abnormal hypobranchial placode', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(54611, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0141748', 'abnormal gas homeostasis', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(54612, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100034', 'abnormal blastomere V1.1', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(54613, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0128071', 'decreased size of the cell part', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(54614, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0139669', 'decreased cell population proliferation in ventro-lateral region', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(54615, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0141776', 'abnormal metabolic process', 0.5238095238095238, 4.758907843651163, 1.5788480773767701, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(54616, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0136516', 'increased cell population proliferation in axial region', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(54617, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0131685', 'abnormal cortical actin cytoskeleton', 0.5652173913043478, 3.6715585125471644, 1.440565418328227, 'UPHENO:0086172', 'abnormal cell'),
(54618, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100069', 'abnormal urinary system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(54619, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0131551', 'abnormally localised actin cytoskeleton', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(54620, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100713', 'abnormal monociliated cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(54621, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0135615', 'increased cell population proliferation in acellular anatomical structure', 0.4166666666666667, 5.835653092541957, 1.5593338712067029, 'HP:0011017', 'Abnormal cellular physiology'),
(54622, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0125523', 'absent acid secreting cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(54623, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0139670', 'decreased cell population proliferation in dorso-lateral region', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(54624, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0127168', 'abnormally localised chondroblast', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(54625, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0102323', 'abnormal keratin accumulating cell morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(54626, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0141299', 'abnormal actin filament morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(54627, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0141285', 'abnormal cortical actin cytoskeleton morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(54628, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100791', 'abnormal multiciliated cell precursor', 0.6190476190476191, 3.6715585125471644, 1.5076039119696991, 'UPHENO:0086172', 'abnormal cell'),
(54629, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100363', 'abnormal cardiovascular system', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(54630, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0101485', 'abnormal descending interneuron', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(54631, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0107259', 'abnormal animal-vegetal axis', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(54632, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0131032', 'abnormally increased number of acid secreting cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(54633, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0101468', 'abnormal stage I oocyte', 0.5652173913043478, 3.6715585125471644, 1.440565418328227, 'UPHENO:0086172', 'abnormal cell'),
(54634, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0139618', 'decreased cell population proliferation in axial region', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(54635, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0101228', 'abnormal mesenchymal stem cell', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(54636, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0101311', 'abnormal bottle cell', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(54637, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0101514', 'abnormal dendrite', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(54638, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0141264', 'abnormal schooling behavior', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(54639, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0138577', 'decreased cell population proliferation in anatomical group', 0.4166666666666667, 5.835653092541957, 1.5593338712067029, 'HP:0011017', 'Abnormal cellular physiology'),
(54640, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0126159', 'absent apoptotic cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(54641, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0141904', 'abnormal glucosamine metabolic process', 0.4782608695652174, 4.758907843651163, 1.508641575552437, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(54642, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0107264', 'abnormal anterior side', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(54643, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0125053', 'absent zygote', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(54644, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0138818', 'decreased cell population proliferation in portion of organism substance', 0.4411764705882353, 5.835653092541957, 1.6045413160604438, 'HP:0011017', 'Abnormal cellular physiology'),
(54645, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0125859', 'absent nucleate erythrocyte', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(54646, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100032', 'abnormal nervous system', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(54647, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100823', 'abnormal blood', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(54648, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100396', 'abnormal dorsal animal hemisphere blastomere', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(54649, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100643', 'abnormal thoracic region', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(54650, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0141898', 'abnormal maltose metabolic process', 0.4230769230769231, 4.758907843651163, 1.418937661667548, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(54651, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0131328', 'abnormally decreased number of paracrine cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(54652, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0125715', 'absent barrier cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(54653, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0131383', 'abnormally decreased number of cementoblast', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(54654, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0101480', 'abnormal stage V oocyte', 0.5652173913043478, 3.6715585125471644, 1.440565418328227, 'UPHENO:0086172', 'abnormal cell'),
(54655, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0127794', 'abnormally localised mitotic cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(54656, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0139500', 'decreased cell population proliferation in egg jelly', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(54657, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100339', 'abnormal circumblastoporal collar', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(54658, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0126628', 'abnormally localised blastomere', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(54659, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100196', 'abnormal neuron', 0.5, 3.6715585125471644, 1.3549093166236559, 'UPHENO:0086172', 'abnormal cell'),
(54660, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100754', 'abnormal electrically active cell', 0.6190476190476191, 3.6715585125471644, 1.5076039119696991, 'UPHENO:0086172', 'abnormal cell'),
(54661, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0103894', 'abnormally decreased number of spindle microtubule', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(54662, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0131351', 'abnormally decreased number of apoptotic cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(54663, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0101198', 'abnormal digestive enzyme secreting cell', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(54664, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100202', 'abnormal embryo', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(54665, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0101503', 'abnormal organ cortex', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(54666, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0101513', 'abnormal basal body', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(54667, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0141795', 'abnormal glycosylation', 0.44, 4.758907843651163, 1.447038165082909, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(54668, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0101405', 'abnormal ring structure', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(54669, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100081', 'abnormal anatomical entity in vitro', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(54670, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0135322', 'increased cell population proliferation in marginal zone (sensu neural)', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(54671, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0102069', 'abnormal proepicardium morphology', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(54672, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0103021', 'abnormal wedge region morphology', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(54673, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0102539', 'abnormal cytoplasm morphology', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(54674, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0107323', 'abnormal thrombocyte', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(54675, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0102285', 'abnormal myoblast morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(54676, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0101576', 'abnormal blastomere V1.2.2', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(54677, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100295', 'abnormal extracellular matrix', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(54678, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0103636', 'abnormally increased number of melanoblast', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(54679, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100569', 'abnormal motor axon', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(54680, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0131569', 'abnormally localised cortical actin cytoskeleton', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(54681, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100901', 'abnormal blastomere D1.2.2', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(54682, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100258', 'abnormal organ part', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(54683, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0141296', 'abnormal adherens junction morphology', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(54684, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0135483', 'increased cell population proliferation in organism subdivision', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(54685, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0131523', 'absent actin filament', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(54686, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0102183', 'abnormal oocyte cortex morphology', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(54687, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100026', 'abnormal germ cell', 0.6190476190476191, 3.6715585125471644, 1.5076039119696991, 'UPHENO:0086172', 'abnormal cell'),
(54688, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100654', 'abnormal blastomere V2.1', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(54689, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0131559', 'abnormally localised spindle microtubule', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(54690, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0101358', 'abnormal endothelial cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(54691, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0127196', 'abnormally localised electrically active cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(54692, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0127338', 'abnormally localised mucus secreting cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(54693, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100162', 'abnormal presumptive rhombomere', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(54694, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100273', 'abnormal visual system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(54695, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0116494', 'absent biological process', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(54696, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0131130', 'abnormally increased number of myelin accumulating cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(54697, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0127257', 'abnormally localised wedge region', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(54698, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0101022', 'abnormal blastomere V1.2', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(54699, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0127364', 'abnormally localised multiciliated cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(54700, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100843', 'abnormal fasciculated network of fibrils', 0.5, 3.6715585125471644, 1.3549093166236559, 'UPHENO:0086172', 'abnormal cell'),
(54701, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0135718', 'increased cell population proliferation in anatomical line', 0.4411764705882353, 5.835653092541957, 1.6045413160604438, 'HP:0011017', 'Abnormal cellular physiology'),
(54702, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100989', 'abnormal right blastomere', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(54703, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0131278', 'abnormally decreased number of keratin accumulating cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(54704, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0107278', 'abnormal medial region', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(54705, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100956', 'abnormal centrosome', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(54706, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100585', 'abnormal elastica externa', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(54707, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100912', 'abnormal trabecula', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(54708, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0136515', 'increased cell population proliferation in apical region', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(54709, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0131066', 'abnormally increased number of myoblast', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(54710, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0101490', 'abnormal ectodermal cell', 0.48148148148148145, 3.6715585125471644, 1.3295816755533123, 'UPHENO:0086172', 'abnormal cell'),
(54711, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0141782', 'abnormal methylation', 0.4782608695652174, 4.758907843651163, 1.508641575552437, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(54712, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0103414', 'abnormally increased number of vacuole in the spermatozoon', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(54713, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100493', 'abnormal liver and biliary system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(54714, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0141880', 'abnormal ethanolamine metabolic process', 0.4074074074074074, 4.758907843651163, 1.392413123563799, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(54715, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100285', 'abnormal progenitor cell', 0.6190476190476191, 3.6715585125471644, 1.5076039119696991, 'UPHENO:0086172', 'abnormal cell'),
(54716, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0131110', 'abnormally increased number of paracrine cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(54717, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0127391', 'abnormally localised lampbrush chromosome', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(54718, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0131297', 'abnormally decreased number of melanoblast', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(54719, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0101133', 'abnormal motor neuron', 0.48148148148148145, 3.6715585125471644, 1.3295816755533123, 'UPHENO:0086172', 'abnormal cell'),
(54720, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100842', 'abnormal left-dorsal blastomere', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(54721, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0141267', 'abnormal resting posture', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(54722, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0124864', 'absent germ cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(54723, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0135476', 'increased cell population proliferation in anatomical system', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(54724, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0101120', 'abnormal cardiac progenitor cell', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(54725, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0116434', 'abnormal biological process', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(54726, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0141783', 'abnormal collagen metabolic process', 0.4782608695652174, 4.758907843651163, 1.508641575552437, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(54727, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0141714', 'abnormal anterior notochord', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(54728, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0141767', 'abnormal temperature homeostasis', 0.4074074074074074, 4.758907843651163, 1.392413123563799, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(54729, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0102109', 'abnormal pericyte morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(54730, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0131189', 'abnormally decreased number of stem cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(54731, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100307', 'abnormal blastomere', 0.5652173913043478, 3.6715585125471644, 1.440565418328227, 'UPHENO:0086172', 'abnormal cell'),
(54732, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0126082', 'absent perivitelline space', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(54733, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100993', 'abnormal ligament cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(54734, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100638', 'abnormal polar body', 0.6190476190476191, 3.6715585125471644, 1.5076039119696991, 'UPHENO:0086172', 'abnormal cell'),
(54735, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100574', 'abnormal gastrula cell', 0.5652173913043478, 3.6715585125471644, 1.440565418328227, 'UPHENO:0086172', 'abnormal cell'),
(54736, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0101498', 'abnormal stage II oocyte', 0.5652173913043478, 3.6715585125471644, 1.440565418328227, 'UPHENO:0086172', 'abnormal cell'),
(54737, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0131195', 'abnormally decreased number of Merkel cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(54738, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0127896', 'abnormally localised ring structure', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(54739, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0142065', 'abnormally decreased number of desmosome', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(54740, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100416', 'abnormal ligament', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(54741, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0131300', 'abnormally decreased number of alkali secreting cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(54742, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0107287', 'abnormal afferent neuron', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(54743, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0102526', 'abnormal nucleus morphology', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(54744, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0127486', 'abnormally localised kinetochore', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(54745, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0138581', 'decreased cell population proliferation in male organism', 0.4166666666666667, 5.835653092541957, 1.5593338712067029, 'HP:0011017', 'Abnormal cellular physiology'),
(54746, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0101411', 'abnormal marginal zone (sensu neural)', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(54747, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0101269', 'abnormal mesodermal cell', 0.48148148148148145, 3.6715585125471644, 1.3295816755533123, 'UPHENO:0086172', 'abnormal cell'),
(54748, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0139127', 'decreased cell population proliferation in joint region', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(54749, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0131205', 'abnormally decreased number of ciliated cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(54750, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0101107', 'abnormal erythroid cell', 0.5, 3.6715585125471644, 1.3549093166236559, 'UPHENO:0086172', 'abnormal cell'),
(54751, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0101239', 'abnormal olfactory epithelial support cell', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(54752, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0125997', 'absent Merkel cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(54753, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0101587', 'abnormal hemangioblast', 0.5, 3.6715585125471644, 1.3549093166236559, 'UPHENO:0086172', 'abnormal cell'),
(54754, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0101200', 'abnormal joint region', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(54755, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0101074', 'abnormal germinal vesicle', 0.52, 3.6715585125471644, 1.3817418089225373, 'UPHENO:0086172', 'abnormal cell'),
(54756, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0127089', 'abnormally localised myoblast', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(54757, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0142056', 'abnormal main body axis', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(54758, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0127806', 'abnormally localised spermatid', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(54759, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0101547', 'abnormal lampbrush chromosome', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(54760, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100437', 'abnormal proepicardium', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(54761, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0127435', 'abnormally localised mitotic spindle', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(54762, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100423', 'abnormal process', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(54763, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0102353', 'abnormal centromere morphology', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(54764, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100882', 'abnormal perichondrial cell', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(54765, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100070', 'abnormal anatomical system', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(54766, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100581', 'abnormal immune system', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(54767, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100573', 'abnormal extraembryonic structure', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(54768, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0107270', 'abnormal proximal-distal axis', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(54769, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100781', 'abnormal presumptive ectoderm', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(54770, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0107288', 'abnormal larval alimentary system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(54771, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0131707', 'abnormal cilium assembly', 0.5172413793103449, 5.835653092541957, 1.7373661832679608, 'HP:0011017', 'Abnormal cellular physiology'),
(54772, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100915', 'abnormal dermal system', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(54773, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100902', 'abnormal spermatocyte', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(54774, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0131531', 'absent cortical actin cytoskeleton', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(54775, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0101326', 'abnormal cementoblast', 0.6190476190476191, 3.6715585125471644, 1.5076039119696991, 'UPHENO:0086172', 'abnormal cell'),
(54776, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0131145', 'abnormally increased number of polar body', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(54777, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0102306', 'abnormal secondary oogonium morphology', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(54778, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100701', 'abnormal microglial cell', 0.48148148148148145, 3.6715585125471644, 1.3295816755533123, 'UPHENO:0086172', 'abnormal cell'),
(54779, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100547', 'abnormal blastomere V2', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(54780, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0101004', 'abnormal acid secreting cell', 0.6190476190476191, 3.6715585125471644, 1.5076039119696991, 'UPHENO:0086172', 'abnormal cell'),
(54781, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0126472', 'abnormally localised secondary spermatogonium', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(54782, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0126162', 'absent alkali secreting cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(54783, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0138838', 'decreased cell population proliferation in cell condensation', 0.4166666666666667, 5.835653092541957, 1.5593338712067029, 'HP:0011017', 'Abnormal cellular physiology'),
(54784, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100544', 'abnormal neuromast support cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(54785, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0131153', 'abnormally increased number of electrically active cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(54786, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0131096', 'abnormally increased number of exocrine cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(54787, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0103005', 'abnormal oxygen accumulating cell morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(54788, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0133438', 'abnormal cilium morphology in the ciliated non-epidermal cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(54789, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0126388', 'abnormally localised oocyte', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(54790, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100907', 'abnormal cytoplasm', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(54791, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100917', 'abnormal stage III oocyte', 0.5652173913043478, 3.6715585125471644, 1.440565418328227, 'UPHENO:0086172', 'abnormal cell'),
(54792, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0101061', 'abnormal plasma membrane', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(54793, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100289', 'abnormal chondroblast', 0.6190476190476191, 3.6715585125471644, 1.5076039119696991, 'UPHENO:0086172', 'abnormal cell'),
(54794, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0107285', 'abnormal flexural organ', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(54795, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100665', 'abnormal egg jelly', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(54796, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0141315', 'abnormal anatomical region', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(54797, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0131204', 'abnormally decreased number of pericyte', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(54798, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100277', 'abnormal blastocoel', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(54799, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100398', 'abnormal vegetal blastomere', 0.48148148148148145, 3.6715585125471644, 1.3295816755533123, 'UPHENO:0086172', 'abnormal cell'),
(54800, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100691', 'abnormal keratin accumulating cell', 0.6190476190476191, 3.6715585125471644, 1.5076039119696991, 'UPHENO:0086172', 'abnormal cell'),
(54801, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100377', 'abnormal connective tissue', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(54802, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100546', 'abnormal whole organism', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(54803, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0141877', 'abnormal 2-deoxyribose 1-phosphate metabolic process', 0.4230769230769231, 4.758907843651163, 1.418937661667548, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(54804, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0101071', 'abnormal endoplasmic reticulum', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(54805, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0125577', 'absent cilium', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(54806, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0102434', 'abnormal exocrine cell morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(54807, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0101166', 'abnormal premigratory neural crest cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(54808, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100501', 'abnormal urogenital system', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(54809, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0101373', 'abnormal oxygen accumulating cell', 0.6190476190476191, 3.6715585125471644, 1.5076039119696991, 'UPHENO:0086172', 'abnormal cell'),
(54810, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0101450', 'abnormal myeloid cell', 0.5, 3.6715585125471644, 1.3549093166236559, 'UPHENO:0086172', 'abnormal cell'),
(54811, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0131248', 'abnormally decreased number of acid secreting cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(54812, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100965', 'abnormal blastomere V2.2', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(54813, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0138890', 'decreased cell population proliferation in intersomitic region', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(54814, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0141499', 'abnormal tadpole', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(54815, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0125724', 'absent polar body', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(54816, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0141276', 'decreased surface breathing', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(54817, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0101009', 'abnormal blastomere D1.1.1', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(54818, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0127643', 'abnormally localised somatic stem cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(54819, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0133471', 'abnormally decreased number of cilium in the ciliated cell', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(54820, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0130964', 'abnormally increased number of cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(54821, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0131134', 'abnormally increased number of barrier cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(54822, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0131561', 'abnormally localised actin filament', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(54823, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0139625', 'decreased cell population proliferation in antero-dorsal region', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(54824, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0138611', 'decreased cell population proliferation in embryonic structure', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(54825, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0136025', 'increased cell population proliferation in joint region', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(54826, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0102181', 'abnormal mitotic cell morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(54827, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0141743', 'abnormal chemical homeostasis within a tissue', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(54828, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0135507', 'increased cell population proliferation in tissue', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(54829, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0127029', 'abnormally localised multiciliated cell precursor', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(54830, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0125692', 'absent oxygen accumulating cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(54831, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0141718', 'abnormal posterior notochord', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(54832, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100913', 'abnormal Brachets cleft', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(54833, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0107260', 'abnormal anterior-posterior axis', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(54834, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0107371', 'abnormal migrating myoblast morphology', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(54835, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0103145', 'abnormal basal body morphology', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(54836, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0131202', 'abnormally decreased number of germ cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(54837, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100515', 'abnormal somatic stem cell', 0.5909090909090909, 3.6715585125471644, 1.4729417174039097, 'UPHENO:0086172', 'abnormal cell'),
(54838, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100610', 'abnormal appendage', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(54839, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100394', 'abnormal marginal zone', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(54840, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0127288', 'abnormally localised pericyte', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(54841, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0131675', 'abnormal spindle microtubule', 0.5652173913043478, 3.6715585125471644, 1.440565418328227, 'UPHENO:0086172', 'abnormal cell'),
(54842, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0101804', 'abnormal stem cell morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(54843, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0131371', 'abnormally decreased number of electrically active cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(54844, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0135720', 'increased cell population proliferation in extraembryonic structure', 0.4166666666666667, 5.835653092541957, 1.5593338712067029, 'HP:0011017', 'Abnormal cellular physiology'),
(54845, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100386', 'abnormal limb', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(54846, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0101221', 'abnormal larval immune system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(54847, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0101569', 'abnormal activin-induced ectoderm', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(54848, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100967', 'abnormal blastomere V2.1.2', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(54849, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0101362', 'abnormal vegetal cortex', 0.52, 3.6715585125471644, 1.3817418089225373, 'UPHENO:0086172', 'abnormal cell'),
(54850, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0107266', 'abnormal dorsal side', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(54851, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0102872', 'abnormal ciliated non-epidermal cell morphology', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(54852, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0131677', 'abnormal actin filament', 0.5652173913043478, 3.6715585125471644, 1.440565418328227, 'UPHENO:0086172', 'abnormal cell'),
(54853, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0126681', 'abnormally localised basal body', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(54854, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0141771', 'abnormal urea homeostasis', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(54855, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0125061', 'absent basal body', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(54856, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0126783', 'abnormally localised exocrine cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(54857, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100786', 'abnormal presumptive axial mesoderm', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(54858, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0107261', 'abnormal dorsal-ventral axis', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(54859, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0101040', 'abnormal axial mesoderm', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(54860, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0136524', 'increased cell population proliferation in antero-ventral region', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(54861, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0101162', 'abnormal stromal cell', 0.48148148148148145, 3.6715585125471644, 1.3295816755533123, 'UPHENO:0086172', 'abnormal cell'),
(54862, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0125384', 'absent ciliated cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(54863, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0101481', 'abnormal skeletal muscle satellite cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(54864, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0103037', 'abnormal ring structure morphology', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(54865, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0141787', 'abnormal hormone metabolic process', 0.4782608695652174, 4.758907843651163, 1.508641575552437, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(54866, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0139627', 'decreased cell population proliferation in postero-dorsal region', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(54867, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100427', 'abnormal olfactory system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(54868, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0130968', 'abnormally increased number of early embryonic cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(54869, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0141911', 'abnormal ribose phosphate metabolic process', 0.4230769230769231, 4.758907843651163, 1.418937661667548, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(54870, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0139620', 'decreased cell population proliferation in anterior region', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(54871, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0141265', 'abnormal escape behavior', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(54872, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0102608', 'abnormal multiciliated cell morphology', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(54873, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0126738', 'abnormally localised paracrine cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(54874, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0103067', 'abnormal paracrine cell morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(54875, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0136520', 'increased cell population proliferation in dorsal region', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(54876, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100458', 'abnormal autopod', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(54877, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0141792', 'abnormal small molecule metabolic process', 0.4782608695652174, 4.758907843651163, 1.508641575552437, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(54878, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0141438', 'increased cell population proliferation in tadpole', 0.4166666666666667, 5.835653092541957, 1.5593338712067029, 'HP:0011017', 'Abnormal cellular physiology'),
(54879, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100205', 'abnormal limb segment', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(54880, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0126314', 'absent absorptive cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(54881, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0127533', 'abnormally localised spermatocyte', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(54882, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0107276', 'abnormal dorsal region', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(54883, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0125743', 'absent lampbrush chromosome', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(54884, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0102165', 'abnormal melanoblast morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(54885, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0126737', 'abnormally localised mesenchymal stem cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(54886, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0103093', 'abnormal sperm entry point morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(54887, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0131654', 'abnormal neuron projection', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(54888, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0101969', 'abnormal zygote morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(54889, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0127343', 'abnormally localised filopodium', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(54890, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0131694', 'abnormal RNA polymerase II activity', 0.4230769230769231, 4.758907843651163, 1.418937661667548, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(54891, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100549', 'abnormal mitotic cell', 0.6190476190476191, 3.6715585125471644, 1.5076039119696991, 'UPHENO:0086172', 'abnormal cell'),
(54892, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100135', 'abnormal surface structure', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(54893, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100784', 'abnormal left blastomere', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(54894, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0100817', 'abnormal intersomitic neuron', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(54895, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0130979', 'abnormally increased number of Merkel cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(54896, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0107311', 'abnormal apical junction complex', 0.5, 3.6715585125471644, 1.3549093166236559, 'UPHENO:0086172', 'abnormal cell'),
(54897, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0131553', 'abnormally localised Roux spot', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(54898, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0131247', 'abnormally decreased number of nucleate erythrocyte', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(54899, 'HP:0034985', 'Reduced cellular cobalamin uptake', 'XPO:0102869', 'abnormal mucus secreting cell morphology', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(54900, 'HP:0045017', 'Congenital malformation of the left heart', 'XPO:0102601', 'abnormal disaggregated/reaggregated ectoderm treated with activin morphology', 0.4074074074074074, 2.485033483301678, 1.006191357919822, 'UPHENO:0076692', 'abnormal anatomical entity morphology'),
(54901, 'HP:0045017', 'Congenital malformation of the left heart', 'XPO:0101206', 'abnormal ischiadic vein', 0.4117647058823529, 5.249153838287537, 1.4701755971154233, 'UPHENO:0080362', 'abnormal cardiovascular system'),
(54902, 'HP:0045017', 'Congenital malformation of the left heart', 'XPO:0101467', 'abnormal alkali secreting cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(54903, 'HP:0045017', 'Congenital malformation of the left heart', 'XPO:0100638', 'abnormal polar body', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(54904, 'HP:0045017', 'Congenital malformation of the left heart', 'XPO:0128481', 'decreased size of the circulatory system', 0.4146341463414634, 5.9590888072311134, 1.57189112236161, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(54905, 'HP:0045017', 'Congenital malformation of the left heart', 'XPO:0101995', 'abnormal cardiovascular system morphology', 0.5151515151515151, 5.9590888072311134, 1.752094069383132, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(54906, 'HP:0045017', 'Congenital malformation of the left heart', 'XPO:0102742', 'abnormal cell-free extract morphology', 0.4074074074074074, 2.485033483301678, 1.006191357919822, 'UPHENO:0076692', 'abnormal anatomical entity morphology'),
(54907, 'HP:0045017', 'Congenital malformation of the left heart', 'XPO:0100026', 'abnormal germ cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(54908, 'HP:0045017', 'Congenital malformation of the left heart', 'XPO:0101713', 'abnormal anatomical entity in vitro morphology', 0.44, 2.485033483301678, 1.0456647324323118, 'UPHENO:0076692', 'abnormal anatomical entity morphology'),
(54909, 'HP:0045017', 'Congenital malformation of the left heart', 'XPO:0139811', 'abnormally necrotic circulatory system', 0.4358974358974359, 5.9590888072311134, 1.6116921329326988, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(54910, 'HP:0045017', 'Congenital malformation of the left heart', 'XPO:0101431', 'abnormal ischiadic artery', 0.4117647058823529, 5.249153838287537, 1.4701755971154233, 'UPHENO:0080362', 'abnormal cardiovascular system'),
(54911, 'HP:0045017', 'Congenital malformation of the left heart', 'XPO:0100980', 'abnormal dorsal longitudinal anastomosing vessel - left branch', 0.4117647058823529, 5.249153838287537, 1.4701755971154233, 'UPHENO:0080362', 'abnormal cardiovascular system'),
(54912, 'HP:0045017', 'Congenital malformation of the left heart', 'XPO:0140144', 'abnormally necrotic portion of organism substance', 0.4074074074074074, 2.485033483301678, 1.006191357919822, 'UPHENO:0076692', 'abnormal anatomical entity morphology'),
(54913, 'HP:0045017', 'Congenital malformation of the left heart', 'XPO:0100852', 'abnormal interdigital region', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(54914, 'HP:0045017', 'Congenital malformation of the left heart', 'XPO:0100080', 'abnormal aorta', 0.4117647058823529, 5.249153838287537, 1.4701755971154233, 'UPHENO:0080362', 'abnormal cardiovascular system'),
(54915, 'HP:0045017', 'Congenital malformation of the left heart', 'XPO:0100780', 'abnormal vascular plexus', 0.42424242424242425, 5.249153838287537, 1.4922847414540332, 'UPHENO:0080362', 'abnormal cardiovascular system'),
(54916, 'HP:0045017', 'Congenital malformation of the left heart', 'XPO:0101694', 'abnormal anatomical space morphology', 0.4074074074074074, 2.485033483301678, 1.006191357919822, 'UPHENO:0076692', 'abnormal anatomical entity morphology'),
(54917, 'HP:0045017', 'Congenital malformation of the left heart', 'XPO:0141316', 'abnormal anatomical region morphology', 0.4074074074074074, 2.485033483301678, 1.006191357919822, 'UPHENO:0076692', 'abnormal anatomical entity morphology'),
(54918, 'HP:0045017', 'Congenital malformation of the left heart', 'XPO:0102113', 'abnormal anatomical line morphology', 0.44, 2.485033483301678, 1.0456647324323118, 'UPHENO:0076692', 'abnormal anatomical entity morphology'),
(54919, 'HP:0045017', 'Congenital malformation of the left heart', 'XPO:0100792', 'abnormal capillary', 0.42424242424242425, 5.249153838287537, 1.4922847414540332, 'UPHENO:0080362', 'abnormal cardiovascular system'),
(54920, 'HP:0045017', 'Congenital malformation of the left heart', 'XPO:0102800', 'abnormal circulating cell morphology', 0.4473684210526316, 5.9590888072311134, 1.6327608981732116, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(54921, 'HP:0045017', 'Congenital malformation of the left heart', 'XPO:0100802', 'abnormal exocrine cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(54922, 'HP:0045017', 'Congenital malformation of the left heart', 'XPO:0100108', 'abnormal cell part', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(54923, 'HP:0045017', 'Congenital malformation of the left heart', 'XPO:0101535', 'abnormal absorptive cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(54924, 'HP:0045017', 'Congenital malformation of the left heart', 'XPO:0102649', 'abnormal outflow tract morphology', 0.41304347826086957, 7.414388317771038, 1.74998992567069, 'UPHENO:0076810', 'abnormal heart morphology'),
(54925, 'HP:0045017', 'Congenital malformation of the left heart', 'XPO:0141112', 'abnormally necrotic angioblast', 0.40476190476190477, 5.9590888072311134, 1.5530653998657664, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(54926, 'HP:0045017', 'Congenital malformation of the left heart', 'XPO:0101237', 'abnormal mucus secreting cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(54927, 'HP:0045017', 'Congenital malformation of the left heart', 'XPO:0101585', 'abnormal dorsal longitudinal anastomosing vessel - right branch', 0.4117647058823529, 5.249153838287537, 1.4701755971154233, 'UPHENO:0080362', 'abnormal cardiovascular system'),
(54928, 'HP:0045017', 'Congenital malformation of the left heart', 'XPO:0100789', 'abnormal occipitovertebral artery', 0.4117647058823529, 5.249153838287537, 1.4701755971154233, 'UPHENO:0080362', 'abnormal cardiovascular system'),
(54929, 'HP:0045017', 'Congenital malformation of the left heart', 'XPO:0101448', 'abnormal myelin accumulating cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(54930, 'HP:0045017', 'Congenital malformation of the left heart', 'XPO:0101636', 'abnormal cell morphology', 0.40625, 2.485033483301678, 1.004761092295729, 'UPHENO:0076692', 'abnormal anatomical entity morphology'),
(54931, 'HP:0045017', 'Congenital malformation of the left heart', 'XPO:0100653', 'abnormal myoblast', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(54932, 'HP:0045017', 'Congenital malformation of the left heart', 'XPO:0100285', 'abnormal progenitor cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(54933, 'HP:0045017', 'Congenital malformation of the left heart', 'XPO:0100477', 'abnormal pericyte', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(54934, 'HP:0045017', 'Congenital malformation of the left heart', 'XPO:0100337', 'abnormal zygote', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(54935, 'HP:0045017', 'Congenital malformation of the left heart', 'XPO:0100006', 'abnormal anatomical structure', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(54936, 'HP:0045017', 'Congenital malformation of the left heart', 'XPO:0101740', 'abnormal cell part morphology', 0.41935483870967744, 2.485033483301678, 1.0208382906112619, 'UPHENO:0076692', 'abnormal anatomical entity morphology'),
(54937, 'HP:0045017', 'Congenital malformation of the left heart', 'XPO:0100172', 'abnormal stem cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(54938, 'HP:0045017', 'Congenital malformation of the left heart', 'XPO:0139990', 'abnormally necrotic cardiovascular system', 0.4358974358974359, 5.9590888072311134, 1.6116921329326988, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(54939, 'HP:0045017', 'Congenital malformation of the left heart', 'XPO:0100043', 'abnormal vein', 0.42424242424242425, 5.249153838287537, 1.4922847414540332, 'UPHENO:0080362', 'abnormal cardiovascular system'),
(54940, 'HP:0045017', 'Congenital malformation of the left heart', 'XPO:0140104', 'abnormally necrotic circulating cell', 0.40476190476190477, 5.9590888072311134, 1.5530653998657664, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(54941, 'HP:0045017', 'Congenital malformation of the left heart', 'XPO:0100691', 'abnormal keratin accumulating cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(54942, 'HP:0045017', 'Congenital malformation of the left heart', 'XPO:0101241', 'abnormal nucleate erythrocyte', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(54943, 'HP:0045017', 'Congenital malformation of the left heart', 'XPO:0101583', 'abnormal truncus arteriosus', 0.42424242424242425, 5.249153838287537, 1.4922847414540332, 'UPHENO:0080362', 'abnormal cardiovascular system'),
(54944, 'HP:0045017', 'Congenital malformation of the left heart', 'XPO:0101890', 'abnormal organ part morphology', 0.4074074074074074, 2.485033483301678, 1.006191357919822, 'UPHENO:0076692', 'abnormal anatomical entity morphology'),
(54945, 'HP:0045017', 'Congenital malformation of the left heart', 'XPO:0101333', 'abnormal barrier epithelial cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(54946, 'HP:0045017', 'Congenital malformation of the left heart', 'XPO:0128032', 'decreased size of the cardiovascular system', 0.4146341463414634, 5.9590888072311134, 1.57189112236161, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(54947, 'HP:0045017', 'Congenital malformation of the left heart', 'XPO:0102773', 'abnormal Keller explant morphology', 0.4074074074074074, 2.485033483301678, 1.006191357919822, 'UPHENO:0076692', 'abnormal anatomical entity morphology'),
(54948, 'HP:0045017', 'Congenital malformation of the left heart', 'XPO:0100481', 'abnormal anatomical line', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(54949, 'HP:0045017', 'Congenital malformation of the left heart', 'XPO:0100081', 'abnormal anatomical entity in vitro', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(54950, 'HP:0045017', 'Congenital malformation of the left heart', 'XPO:0102178', 'abnormal whole organism morphology', 0.4074074074074074, 2.485033483301678, 1.006191357919822, 'UPHENO:0076692', 'abnormal anatomical entity morphology'),
(54951, 'HP:0045017', 'Congenital malformation of the left heart', 'XPO:0101004', 'abnormal acid secreting cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(54952, 'HP:0045017', 'Congenital malformation of the left heart', 'XPO:0100754', 'abnormal electrically active cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(54953, 'HP:0045017', 'Congenital malformation of the left heart', 'XPO:0103024', 'abnormal sinus venosus morphology', 0.41304347826086957, 7.414388317771038, 1.74998992567069, 'UPHENO:0076810', 'abnormal heart morphology'),
(54954, 'HP:0045017', 'Congenital malformation of the left heart', 'XPO:0107345', 'abnormal anatomical axis morphology', 0.4074074074074074, 2.485033483301678, 1.006191357919822, 'UPHENO:0076692', 'abnormal anatomical entity morphology'),
(54955, 'HP:0045017', 'Congenital malformation of the left heart', 'XPO:0100987', 'abnormal larval aorta', 0.4117647058823529, 5.249153838287537, 1.4701755971154233, 'UPHENO:0080362', 'abnormal cardiovascular system'),
(54956, 'HP:0045017', 'Congenital malformation of the left heart', 'XPO:0101243', 'abnormal vertebral artery', 0.4117647058823529, 5.249153838287537, 1.4701755971154233, 'UPHENO:0080362', 'abnormal cardiovascular system'),
(54957, 'HP:0045017', 'Congenital malformation of the left heart', 'XPO:0101919', 'abnormal heart primordium morphology', 0.4473684210526316, 5.9590888072311134, 1.6327608981732116, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(54958, 'HP:0045017', 'Congenital malformation of the left heart', 'XPO:0101686', 'abnormal blood vessel morphology', 0.4146341463414634, 5.9590888072311134, 1.57189112236161, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(54959, 'HP:0045017', 'Congenital malformation of the left heart', 'XPO:0100791', 'abnormal multiciliated cell precursor', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(54960, 'HP:0045017', 'Congenital malformation of the left heart', 'XPO:0100004', 'abnormal cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(54961, 'HP:0045017', 'Congenital malformation of the left heart', 'XPO:0100549', 'abnormal mitotic cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(54962, 'HP:0045017', 'Congenital malformation of the left heart', 'XPO:0101976', 'abnormal portion of organism substance morphology', 0.44, 2.485033483301678, 1.0456647324323118, 'UPHENO:0076692', 'abnormal anatomical entity morphology'),
(54963, 'HP:0045017', 'Congenital malformation of the left heart', 'XPO:0102532', 'abnormal angioblast morphology', 0.4473684210526316, 5.9590888072311134, 1.6327608981732116, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(54964, 'HP:0045017', 'Congenital malformation of the left heart', 'XPO:0101373', 'abnormal oxygen accumulating cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(54965, 'HP:0045017', 'Congenital malformation of the left heart', 'XPO:0102233', 'abnormal vascular endothelium morphology', 0.40476190476190477, 5.9590888072311134, 1.5530653998657664, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(54966, 'HP:0045017', 'Congenital malformation of the left heart', 'XPO:0100344', 'abnormal portion of organism substance', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(54967, 'HP:0045017', 'Congenital malformation of the left heart', 'XPO:0100522', 'abnormal subinterstitial vein', 0.4117647058823529, 5.249153838287537, 1.4701755971154233, 'UPHENO:0080362', 'abnormal cardiovascular system'),
(54968, 'HP:0045017', 'Congenital malformation of the left heart', 'XPO:0101132', 'abnormal apoptotic cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(54969, 'HP:0045017', 'Congenital malformation of the left heart', 'XPO:0100137', 'abnormal cardinal vein', 0.4117647058823529, 5.249153838287537, 1.4701755971154233, 'UPHENO:0080362', 'abnormal cardiovascular system'),
(54970, 'HP:0045017', 'Congenital malformation of the left heart', 'XPO:0101557', 'abnormal Jacobsons vein', 0.4117647058823529, 5.249153838287537, 1.4701755971154233, 'UPHENO:0080362', 'abnormal cardiovascular system'),
(54971, 'HP:0045017', 'Congenital malformation of the left heart', 'XPO:0100715', 'abnormal ciliated cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(54972, 'HP:0045017', 'Congenital malformation of the left heart', 'XPO:0141328', 'edematous circulatory system', 0.4722222222222222, 5.9590888072311134, 1.6775023573665249, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(54973, 'HP:0045017', 'Congenital malformation of the left heart', 'XPO:0100076', 'abnormal artery', 0.42424242424242425, 5.249153838287537, 1.4922847414540332, 'UPHENO:0080362', 'abnormal cardiovascular system'),
(54974, 'HP:0045017', 'Congenital malformation of the left heart', 'XPO:0101297', 'abnormal barrier cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(54975, 'HP:0045017', 'Congenital malformation of the left heart', 'XPO:0100054', 'abnormal blood vessel', 0.4375, 5.249153838287537, 1.5154223187781013, 'UPHENO:0080362', 'abnormal cardiovascular system'),
(54976, 'HP:0045017', 'Congenital malformation of the left heart', 'XPO:0129512', 'increased size of the cardiovascular system', 0.4146341463414634, 5.9590888072311134, 1.57189112236161, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(54977, 'HP:0045017', 'Congenital malformation of the left heart', 'XPO:0141283', 'abnormal atrioventricular valve morphology', 0.40425531914893614, 7.414388317771038, 1.7312729177384698, 'UPHENO:0076810', 'abnormal heart morphology'),
(54978, 'HP:0045017', 'Congenital malformation of the left heart', 'XPO:0100704', 'abnormal Merkel cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(54979, 'HP:0045017', 'Congenital malformation of the left heart', 'XPO:0100933', 'abnormal branchial vein', 0.4117647058823529, 5.249153838287537, 1.4701755971154233, 'UPHENO:0080362', 'abnormal cardiovascular system'),
(54980, 'HP:0045017', 'Congenital malformation of the left heart', 'XPO:0140420', 'abnormally necrotic bulbous arteriosis', 0.4146341463414634, 5.9590888072311134, 1.57189112236161, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(54981, 'HP:0045017', 'Congenital malformation of the left heart', 'XPO:0100533', 'abnormal melanoblast', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(54982, 'HP:0045017', 'Congenital malformation of the left heart', 'XPO:0100981', 'abnormal dorsal longitudinal anastomosing vessel', 0.42424242424242425, 5.249153838287537, 1.4922847414540332, 'UPHENO:0080362', 'abnormal cardiovascular system'),
(54983, 'HP:0045017', 'Congenital malformation of the left heart', 'XPO:0140269', 'abnormally necrotic anatomical line', 0.4074074074074074, 2.485033483301678, 1.006191357919822, 'UPHENO:0076692', 'abnormal anatomical entity morphology'),
(54984, 'HP:0045017', 'Congenital malformation of the left heart', 'XPO:0101638', 'abnormal anatomical structure morphology', 0.44, 2.485033483301678, 1.0456647324323118, 'UPHENO:0076692', 'abnormal anatomical entity morphology'),
(54985, 'HP:0045017', 'Congenital malformation of the left heart', 'XPO:0102935', 'abnormal bulbous arteriosis morphology', 0.4722222222222222, 5.9590888072311134, 1.6775023573665249, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(54986, 'HP:0045017', 'Congenital malformation of the left heart', 'XPO:0103201', 'abnormal activin-induced ectoderm morphology', 0.4074074074074074, 2.485033483301678, 1.006191357919822, 'UPHENO:0076692', 'abnormal anatomical entity morphology'),
(54987, 'HP:0045017', 'Congenital malformation of the left heart', 'XPO:0101900', 'abnormal circulatory system morphology', 0.5151515151515151, 5.9590888072311134, 1.752094069383132, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(54988, 'HP:0045017', 'Congenital malformation of the left heart', 'XPO:0101326', 'abnormal cementoblast', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(54989, 'HP:0045017', 'Congenital malformation of the left heart', 'XPO:0101770', 'abnormal trunk vasculature morphology', 0.425, 5.9590888072311134, 1.5914184688739863, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(54990, 'HP:0045017', 'Congenital malformation of the left heart', 'XPO:0101435', 'abnormal paracrine cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(54991, 'HP:0045017', 'Congenital malformation of the left heart', 'XPO:0139718', 'abnormally necrotic anatomical structure', 0.4074074074074074, 2.485033483301678, 1.006191357919822, 'UPHENO:0076692', 'abnormal anatomical entity morphology'),
(54992, 'HP:0045017', 'Congenital malformation of the left heart', 'XPO:0100289', 'abnormal chondroblast', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(54993, 'HP:0045017', 'Congenital malformation of the left heart', 'XPO:0129961', 'increased size of the circulatory system', 0.4146341463414634, 5.9590888072311134, 1.57189112236161, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(54994, 'HP:0032201', 'Rotator cuff tear', 'XPO:0102272', 'abnormal notochordal sheath morphology', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(54995, 'HP:0032201', 'Rotator cuff tear', 'XPO:0102806', 'abnormal articular system morphology', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(54996, 'HP:0032201', 'Rotator cuff tear', 'XPO:0141723', 'abnormal posterior notochord morphology', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(54997, 'HP:0032201', 'Rotator cuff tear', 'XPO:0103234', 'abnormal intersomitic tendon morphology', 0.46296296296296297, 10.802658907487096, 2.2363432150921, 'UPHENO:0021425', 'abnormal tendon morphology'),
(54998, 'HP:0032201', 'Rotator cuff tear', 'XPO:0100693', 'abnormal vertebral centrum', 0.40350877192982454, 6.272837960958401, 1.5909573036826314, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(54999, 'HP:0032201', 'Rotator cuff tear', 'XPO:0102054', 'abnormal notochord morphology', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(55000, 'HP:0032201', 'Rotator cuff tear', 'XPO:0130294', 'increased size of the tendon', 0.43103448275862066, 10.802658907487096, 2.1578504337897253, 'UPHENO:0021425', 'abnormal tendon morphology'),
(55001, 'HP:0032201', 'Rotator cuff tear', 'XPO:0141719', 'abnormal anterior notochord morphology', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(55002, 'HP:0032201', 'Rotator cuff tear', 'XPO:0102980', 'abnormal perichordal tissue morphology', 0.44, 6.985637650836012, 1.753191537273622, 'UPHENO:0002712', 'abnormal connective tissue'),
(55003, 'HP:0032201', 'Rotator cuff tear', 'XPO:0102728', 'abnormal tendon morphology', 0.5102040816326531, 10.802658907487096, 2.3476713285903656, 'UPHENO:0021425', 'abnormal tendon morphology'),
(55004, 'HP:0032201', 'Rotator cuff tear', 'XPO:0101957', 'abnormal axial skeleton morphology', 0.4117647058823529, 6.211345574613551, 1.599253852164941, 'UPHENO:0087089', 'abnormal axial skeleton plus cranial skeleton morphology'),
(55005, 'HP:0032201', 'Rotator cuff tear', 'XPO:0102144', 'abnormal cranial skeleton morphology', 0.40384615384615385, 6.211345574613551, 1.5838017617482976, 'UPHENO:0087089', 'abnormal axial skeleton plus cranial skeleton morphology'),
(55006, 'HP:0032201', 'Rotator cuff tear', 'XPO:0128816', 'decreased size of the tendon', 0.43103448275862066, 10.802658907487096, 2.1578504337897253, 'UPHENO:0021425', 'abnormal tendon morphology'),
(55007, 'HP:0032201', 'Rotator cuff tear', 'XPO:0140660', 'abnormally necrotic tendon', 0.44642857142857145, 10.802658907487096, 2.196045442084384, 'UPHENO:0021425', 'abnormal tendon morphology'),
(55008, 'HP:0032201', 'Rotator cuff tear', 'XPO:0107372', 'abnormal flexural organ morphology', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(55009, 'HP:0032201', 'Rotator cuff tear', 'XPO:0102567', 'abnormal skeleton morphology', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(55010, 'HP:0032201', 'Rotator cuff tear', 'XPO:0102514', 'abnormal perichondrial cell morphology', 0.43137254901960786, 6.985637650836012, 1.7359182929989752, 'UPHENO:0002712', 'abnormal connective tissue'),
(55011, 'HP:0032201', 'Rotator cuff tear', 'XPO:0102542', 'abnormal vacuolated notochordal tissue morphology', 0.44, 6.985637650836012, 1.753191537273622, 'UPHENO:0002712', 'abnormal connective tissue'),
(55012, 'HP:0032201', 'Rotator cuff tear', 'XPO:0102010', 'abnormal perichondrium morphology', 0.46808510638297873, 6.985637650836012, 1.808279000305129, 'UPHENO:0002712', 'abnormal connective tissue'),
(55013, 'HP:0032201', 'Rotator cuff tear', 'XPO:0102461', 'abnormal postcranial axial skeleton morphology', 0.4423076923076923, 6.272837960958401, 1.6656903922192745, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(55014, 'HP:0032201', 'Rotator cuff tear', 'XPO:0102217', 'abnormal elastica externa morphology', 0.43478260869565216, 4.638757693672553, 1.4201588541997616, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(55015, 'HP:0032201', 'Rotator cuff tear', 'XPO:0140043', 'abnormally necrotic perichondrium', 0.41509433962264153, 6.985637650836012, 1.7028501541582675, 'UPHENO:0002712', 'abnormal connective tissue'),
(55016, 'HP:0032201', 'Rotator cuff tear', 'XPO:0101982', 'abnormal appendicular skeleton morphology', 0.43137254901960786, 5.732269579595698, 1.5724960223217586, 'HP:0011844', 'Abnormal appendicular skeleton morphology'),
(55017, 'HP:0032201', 'Rotator cuff tear', 'XPO:0101860', 'abnormal skeletal subdivision morphology', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(55018, 'HP:0032201', 'Rotator cuff tear', 'XPO:0102097', 'abnormal skeletal system morphology', 0.43478260869565216, 4.638757693672553, 1.4201588541997616, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(55019, 'HP:0032201', 'Rotator cuff tear', 'XPO:0100226', 'abnormal vertebral element', 0.4107142857142857, 6.272837960958401, 1.6050994245019483, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(55020, 'HP:0032201', 'Rotator cuff tear', 'XPO:0100584', 'abnormal vertebral column', 0.46, 6.272837960958401, 1.69867756270602, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(55021, 'HP:0032201', 'Rotator cuff tear', 'XPO:0102216', 'abnormal vertebral column morphology', 0.4107142857142857, 6.272837960958401, 1.6050994245019483, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(55022, 'HP:0032201', 'Rotator cuff tear', 'XPO:0140722', 'abnormally necrotic intersomitic tendon', 0.4032258064516129, 10.802658907487096, 2.0870818981997767, 'UPHENO:0021425', 'abnormal tendon morphology'),
(55023, 'HP:0100306', 'Muscle fiber hyaline bodies', 'XPO:0102471', 'abnormal skeletal myocyte morphology', 0.4230769230769231, 6.895202660022325, 1.7079815939857375, 'HP:0011805', 'Abnormal skeletal muscle morphology'),
(55024, 'HP:0100306', 'Muscle fiber hyaline bodies', 'XPO:0102852', 'abnormal centriole morphology', 0.40476190476190477, 3.6715585125471644, 1.219059890646631, 'UPHENO:0086172', 'abnormal cell'),
(55025, 'HP:0100306', 'Muscle fiber hyaline bodies', 'XPO:0103104', 'abnormal zygote cortex morphology', 0.40476190476190477, 3.6715585125471644, 1.219059890646631, 'UPHENO:0086172', 'abnormal cell'),
(55026, 'HP:0100306', 'Muscle fiber hyaline bodies', 'XPO:0141277', 'abnormal actin cytoskeleton morphology', 0.4146341463414634, 3.6715585125471644, 1.2338369136935103, 'UPHENO:0086172', 'abnormal cell'),
(55027, 'HP:0100306', 'Muscle fiber hyaline bodies', 'XPO:0102024', 'abnormal cilium morphology', 0.40476190476190477, 3.6715585125471644, 1.219059890646631, 'UPHENO:0086172', 'abnormal cell'),
(55028, 'HP:0100306', 'Muscle fiber hyaline bodies', 'XPO:0102873', 'abnormal nucleate erythrocyte morphology', 0.40476190476190477, 3.6715585125471644, 1.219059890646631, 'UPHENO:0086172', 'abnormal cell'),
(55029, 'HP:0100306', 'Muscle fiber hyaline bodies', 'XPO:0103113', 'abnormal skeletal muscle satellite cell morphology', 0.44, 6.895202660022325, 1.7418062953181168, 'HP:0011805', 'Abnormal skeletal muscle morphology'),
(55030, 'HP:0100306', 'Muscle fiber hyaline bodies', 'XPO:0102958', 'abnormal cementoblast morphology', 0.40476190476190477, 3.6715585125471644, 1.219059890646631, 'UPHENO:0086172', 'abnormal cell'),
(55031, 'HP:0100306', 'Muscle fiber hyaline bodies', 'XPO:0141294', 'abnormal sarcomere morphology', 0.44, 6.895202660022325, 1.7418062953181168, 'HP:0011805', 'Abnormal skeletal muscle morphology'),
(55032, 'HP:0100306', 'Muscle fiber hyaline bodies', 'XPO:0128955', 'decreased size of the secondary myofiber', 0.4067796610169492, 7.049658514867893, 1.6934159858000666, 'UPHENO:0067691', 'abnormal morphology of cellular_component'),
(55033, 'HP:0100306', 'Muscle fiber hyaline bodies', 'XPO:0102323', 'abnormal keratin accumulating cell morphology', 0.40476190476190477, 3.6715585125471644, 1.219059890646631, 'UPHENO:0086172', 'abnormal cell'),
(55034, 'HP:0100306', 'Muscle fiber hyaline bodies', 'XPO:0141284', 'abnormal myofibril morphology', 0.4489795918367347, 6.895202660022325, 1.7594900613326552, 'HP:0011805', 'Abnormal skeletal muscle morphology'),
(55035, 'HP:0100306', 'Muscle fiber hyaline bodies', 'XPO:0102353', 'abnormal centromere morphology', 0.4146341463414634, 3.6715585125471644, 1.2338369136935103, 'UPHENO:0086172', 'abnormal cell'),
(55036, 'HP:0100306', 'Muscle fiber hyaline bodies', 'XPO:0102520', 'abnormal microtubule morphology', 0.4146341463414634, 3.6715585125471644, 1.2338369136935103, 'UPHENO:0086172', 'abnormal cell'),
(55037, 'HP:0100306', 'Muscle fiber hyaline bodies', 'XPO:0101804', 'abnormal stem cell morphology', 0.40476190476190477, 3.6715585125471644, 1.219059890646631, 'UPHENO:0086172', 'abnormal cell'),
(55038, 'HP:0100306', 'Muscle fiber hyaline bodies', 'XPO:0139891', 'abnormally necrotic myocyte', 0.41509433962264153, 6.895202660022325, 1.6917918296073688, 'HP:0011805', 'Abnormal skeletal muscle morphology'),
(55039, 'HP:0100306', 'Muscle fiber hyaline bodies', 'XPO:0103179', 'abnormal lampbrush chromosome morphology', 0.4146341463414634, 3.6715585125471644, 1.2338369136935103, 'UPHENO:0086172', 'abnormal cell'),
(55040, 'HP:0100306', 'Muscle fiber hyaline bodies', 'XPO:0102539', 'abnormal cytoplasm morphology', 0.4146341463414634, 3.6715585125471644, 1.2338369136935103, 'UPHENO:0086172', 'abnormal cell'),
(55041, 'HP:0100306', 'Muscle fiber hyaline bodies', 'XPO:0102896', 'abnormal mitotic spindle morphology', 0.4146341463414634, 3.6715585125471644, 1.2338369136935103, 'UPHENO:0086172', 'abnormal cell'),
(55042, 'HP:0100306', 'Muscle fiber hyaline bodies', 'XPO:0102386', 'abnormal electrically active cell morphology', 0.40476190476190477, 3.6715585125471644, 1.219059890646631, 'UPHENO:0086172', 'abnormal cell'),
(55043, 'HP:0100306', 'Muscle fiber hyaline bodies', 'XPO:0102336', 'abnormal Merkel cell morphology', 0.40476190476190477, 3.6715585125471644, 1.219059890646631, 'UPHENO:0086172', 'abnormal cell'),
(55044, 'HP:0100306', 'Muscle fiber hyaline bodies', 'XPO:0107399', 'abnormal filopodium morphology', 0.4146341463414634, 3.6715585125471644, 1.2338369136935103, 'UPHENO:0086172', 'abnormal cell'),
(55045, 'HP:0100306', 'Muscle fiber hyaline bodies', 'XPO:0141073', 'abnormally necrotic skeletal muscle satellite cell', 0.4074074074074074, 6.895202660022325, 1.676053889130166, 'HP:0011805', 'Abnormal skeletal muscle morphology'),
(55046, 'HP:0100306', 'Muscle fiber hyaline bodies', 'XPO:0103005', 'abnormal oxygen accumulating cell morphology', 0.40476190476190477, 3.6715585125471644, 1.219059890646631, 'UPHENO:0086172', 'abnormal cell'),
(55047, 'HP:0100306', 'Muscle fiber hyaline bodies', 'XPO:0102378', 'abnormal smooth muscle morphology', 0.40816326530612246, 6.895202660022325, 1.6776079496301195, 'HP:0011805', 'Abnormal skeletal muscle morphology'),
(55048, 'HP:0100306', 'Muscle fiber hyaline bodies', 'XPO:0101969', 'abnormal zygote morphology', 0.40476190476190477, 3.6715585125471644, 1.219059890646631, 'UPHENO:0086172', 'abnormal cell'),
(55049, 'HP:0100306', 'Muscle fiber hyaline bodies', 'XPO:0102636', 'abnormal acid secreting cell morphology', 0.40476190476190477, 3.6715585125471644, 1.219059890646631, 'UPHENO:0086172', 'abnormal cell'),
(55050, 'HP:0100306', 'Muscle fiber hyaline bodies', 'XPO:0130433', 'increased size of the secondary myofiber', 0.4067796610169492, 7.049658514867893, 1.6934159858000666, 'UPHENO:0067691', 'abnormal morphology of cellular_component'),
(55051, 'HP:0100306', 'Muscle fiber hyaline bodies', 'XPO:0141076', 'abnormally necrotic secondary myofiber', 0.41509433962264153, 6.895202660022325, 1.6917918296073688, 'HP:0011805', 'Abnormal skeletal muscle morphology'),
(55052, 'HP:0100306', 'Muscle fiber hyaline bodies', 'XPO:0102526', 'abnormal nucleus morphology', 0.4146341463414634, 3.6715585125471644, 1.2338369136935103, 'UPHENO:0086172', 'abnormal cell'),
(55053, 'HP:0100306', 'Muscle fiber hyaline bodies', 'XPO:0129985', 'increased size of the myocyte', 0.4067796610169492, 7.049658514867893, 1.6934159858000666, 'UPHENO:0067691', 'abnormal morphology of cellular_component'),
(55054, 'HP:0100306', 'Muscle fiber hyaline bodies', 'XPO:0102347', 'abnormal ciliated cell morphology', 0.40476190476190477, 3.6715585125471644, 1.219059890646631, 'UPHENO:0086172', 'abnormal cell'),
(55055, 'HP:0100306', 'Muscle fiber hyaline bodies', 'XPO:0102285', 'abnormal myoblast morphology', 0.40476190476190477, 3.6715585125471644, 1.219059890646631, 'UPHENO:0086172', 'abnormal cell'),
(55056, 'HP:0100306', 'Muscle fiber hyaline bodies', 'XPO:0102965', 'abnormal barrier epithelial cell morphology', 0.40476190476190477, 3.6715585125471644, 1.219059890646631, 'UPHENO:0086172', 'abnormal cell'),
(55057, 'HP:0100306', 'Muscle fiber hyaline bodies', 'XPO:0103167', 'abnormal absorptive cell morphology', 0.40476190476190477, 3.6715585125471644, 1.219059890646631, 'UPHENO:0086172', 'abnormal cell'),
(55058, 'HP:0100306', 'Muscle fiber hyaline bodies', 'XPO:0103080', 'abnormal myelin accumulating cell morphology', 0.40476190476190477, 3.6715585125471644, 1.219059890646631, 'UPHENO:0086172', 'abnormal cell'),
(55059, 'HP:0100306', 'Muscle fiber hyaline bodies', 'XPO:0101740', 'abnormal cell part morphology', 0.4358974358974359, 3.6715585125471644, 1.2650782352750807, 'UPHENO:0086172', 'abnormal cell'),
(55060, 'HP:0100306', 'Muscle fiber hyaline bodies', 'XPO:0141307', 'abnormal M band morphology', 0.43137254901960786, 6.895202660022325, 1.7246452236505372, 'HP:0011805', 'Abnormal skeletal muscle morphology'),
(55061, 'HP:0100306', 'Muscle fiber hyaline bodies', 'XPO:0103067', 'abnormal paracrine cell morphology', 0.40476190476190477, 3.6715585125471644, 1.219059890646631, 'UPHENO:0086172', 'abnormal cell'),
(55062, 'HP:0100306', 'Muscle fiber hyaline bodies', 'XPO:0102703', 'abnormal endoplasmic reticulum morphology', 0.4146341463414634, 3.6715585125471644, 1.2338369136935103, 'UPHENO:0086172', 'abnormal cell'),
(55063, 'HP:0100306', 'Muscle fiber hyaline bodies', 'XPO:0141299', 'abnormal actin filament morphology', 0.40476190476190477, 3.6715585125471644, 1.219059890646631, 'UPHENO:0086172', 'abnormal cell'),
(55064, 'HP:0100306', 'Muscle fiber hyaline bodies', 'XPO:0102228', 'abnormal myocyte morphology', 0.4489795918367347, 6.895202660022325, 1.7594900613326552, 'HP:0011805', 'Abnormal skeletal muscle morphology'),
(55065, 'HP:0100306', 'Muscle fiber hyaline bodies', 'XPO:0102693', 'abnormal plasma membrane morphology', 0.4146341463414634, 3.6715585125471644, 1.2338369136935103, 'UPHENO:0086172', 'abnormal cell'),
(55066, 'HP:0100306', 'Muscle fiber hyaline bodies', 'XPO:0101732', 'abnormal muscle morphology', 0.43478260869565216, 6.895202660022325, 1.7314485842812966, 'HP:0011805', 'Abnormal skeletal muscle morphology'),
(55067, 'HP:0100306', 'Muscle fiber hyaline bodies', 'XPO:0128505', 'decreased size of the myocyte', 0.4067796610169492, 7.049658514867893, 1.6934159858000666, 'UPHENO:0067691', 'abnormal morphology of cellular_component'),
(55068, 'HP:0100306', 'Muscle fiber hyaline bodies', 'XPO:0102423', 'abnormal multiciliated cell precursor morphology', 0.40476190476190477, 3.6715585125471644, 1.219059890646631, 'UPHENO:0086172', 'abnormal cell'),
(55069, 'HP:0100306', 'Muscle fiber hyaline bodies', 'XPO:0141296', 'abnormal adherens junction morphology', 0.4146341463414634, 3.6715585125471644, 1.2338369136935103, 'UPHENO:0086172', 'abnormal cell'),
(55070, 'HP:0100306', 'Muscle fiber hyaline bodies', 'XPO:0101658', 'abnormal germ cell morphology', 0.40476190476190477, 3.6715585125471644, 1.219059890646631, 'UPHENO:0086172', 'abnormal cell'),
(55071, 'HP:0100306', 'Muscle fiber hyaline bodies', 'XPO:0102869', 'abnormal mucus secreting cell morphology', 0.40476190476190477, 3.6715585125471644, 1.219059890646631, 'UPHENO:0086172', 'abnormal cell'),
(55072, 'HP:0100306', 'Muscle fiber hyaline bodies', 'XPO:0102276', 'abnormal smooth muscle myocyte morphology', 0.41509433962264153, 6.895202660022325, 1.6917918296073688, 'HP:0011805', 'Abnormal skeletal muscle morphology'),
(55073, 'HP:0100306', 'Muscle fiber hyaline bodies', 'XPO:0102764', 'abnormal apoptotic cell morphology', 0.40476190476190477, 3.6715585125471644, 1.219059890646631, 'UPHENO:0086172', 'abnormal cell'),
(55074, 'HP:0100306', 'Muscle fiber hyaline bodies', 'XPO:0102434', 'abnormal exocrine cell morphology', 0.40476190476190477, 3.6715585125471644, 1.219059890646631, 'UPHENO:0086172', 'abnormal cell'),
(55075, 'HP:0100306', 'Muscle fiber hyaline bodies', 'XPO:0103093', 'abnormal sperm entry point morphology', 0.40476190476190477, 3.6715585125471644, 1.219059890646631, 'UPHENO:0086172', 'abnormal cell'),
(55076, 'HP:0100306', 'Muscle fiber hyaline bodies', 'XPO:0142064', 'abnormal desmosome morphology', 0.4146341463414634, 3.6715585125471644, 1.2338369136935103, 'UPHENO:0086172', 'abnormal cell'),
(55077, 'HP:0100306', 'Muscle fiber hyaline bodies', 'XPO:0102165', 'abnormal melanoblast morphology', 0.40476190476190477, 3.6715585125471644, 1.219059890646631, 'UPHENO:0086172', 'abnormal cell'),
(55078, 'HP:0100306', 'Muscle fiber hyaline bodies', 'XPO:0103098', 'abnormal secondary myofiber morphology', 0.4489795918367347, 6.895202660022325, 1.7594900613326552, 'HP:0011805', 'Abnormal skeletal muscle morphology'),
(55079, 'HP:0100306', 'Muscle fiber hyaline bodies', 'XPO:0103099', 'abnormal alkali secreting cell morphology', 0.40476190476190477, 3.6715585125471644, 1.219059890646631, 'UPHENO:0086172', 'abnormal cell'),
(55080, 'HP:0100306', 'Muscle fiber hyaline bodies', 'XPO:0102356', 'abnormal kinetochore morphology', 0.4146341463414634, 3.6715585125471644, 1.2338369136935103, 'UPHENO:0086172', 'abnormal cell'),
(55081, 'HP:0100306', 'Muscle fiber hyaline bodies', 'XPO:0101921', 'abnormal chondroblast morphology', 0.40476190476190477, 3.6715585125471644, 1.219059890646631, 'UPHENO:0086172', 'abnormal cell'),
(55082, 'HP:0100306', 'Muscle fiber hyaline bodies', 'XPO:0102181', 'abnormal mitotic cell morphology', 0.40476190476190477, 3.6715585125471644, 1.219059890646631, 'UPHENO:0086172', 'abnormal cell'),
(55083, 'HP:0100306', 'Muscle fiber hyaline bodies', 'XPO:0102109', 'abnormal pericyte morphology', 0.40476190476190477, 3.6715585125471644, 1.219059890646631, 'UPHENO:0086172', 'abnormal cell'),
(55084, 'HP:0100306', 'Muscle fiber hyaline bodies', 'XPO:0102929', 'abnormal barrier cell morphology', 0.40476190476190477, 3.6715585125471644, 1.219059890646631, 'UPHENO:0086172', 'abnormal cell'),
(55085, 'HP:0100306', 'Muscle fiber hyaline bodies', 'XPO:0101636', 'abnormal cell morphology', 0.425, 3.6715585125471644, 1.249164668021212, 'UPHENO:0086172', 'abnormal cell'),
(55086, 'HP:0100306', 'Muscle fiber hyaline bodies', 'XPO:0103145', 'abnormal basal body morphology', 0.4146341463414634, 3.6715585125471644, 1.2338369136935103, 'UPHENO:0086172', 'abnormal cell'),
(55087, 'HP:0100306', 'Muscle fiber hyaline bodies', 'XPO:0102588', 'abnormal centrosome morphology', 0.4146341463414634, 3.6715585125471644, 1.2338369136935103, 'UPHENO:0086172', 'abnormal cell'),
(55088, 'HP:0100306', 'Muscle fiber hyaline bodies', 'XPO:0141285', 'abnormal cortical actin cytoskeleton morphology', 0.40476190476190477, 3.6715585125471644, 1.219059890646631, 'UPHENO:0086172', 'abnormal cell'),
(55089, 'HP:0100306', 'Muscle fiber hyaline bodies', 'XPO:0101917', 'abnormal progenitor cell morphology', 0.40476190476190477, 3.6715585125471644, 1.219059890646631, 'UPHENO:0086172', 'abnormal cell'),
(55090, 'HP:0100306', 'Muscle fiber hyaline bodies', 'XPO:0101907', 'abnormal skeletal muscle morphology', 0.4166666666666667, 6.895202660022325, 1.6949929522988099, 'HP:0011805', 'Abnormal skeletal muscle morphology'),
(55091, 'HP:0000215', 'Thick upper lip vermilion', 'XPO:0102223', 'abnormal pharyngeal arch morphology', 0.4090909090909091, 5.725717590856133, 1.5304701939081158, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(55092, 'HP:0000215', 'Thick upper lip vermilion', 'XPO:0128105', 'decreased size of the tongue', 0.4430379746835443, 7.884497199543557, 1.8689921537245293, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(55093, 'HP:0000215', 'Thick upper lip vermilion', 'XPO:0129225', 'decreased size of the upper jaw', 0.41379310344827586, 8.81758714901448, 1.9101457408575757, 'UPHENO:0087585', 'abnormal midface morphology'),
(55094, 'HP:0000215', 'Thick upper lip vermilion', 'XPO:0140626', 'abnormally necrotic tongue', 0.49295774647887325, 7.884497199543557, 1.971477611236298, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(55095, 'HP:0000215', 'Thick upper lip vermilion', 'XPO:0103352', 'decreased size of the mouth', 0.4666666666666667, 7.884497199543557, 1.9181845652735452, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(55096, 'HP:0000215', 'Thick upper lip vermilion', 'XPO:0103199', 'abnormal tongue morphology', 0.5303030303030303, 7.884497199543557, 2.044791617092975, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(55097, 'HP:0000215', 'Thick upper lip vermilion', 'XPO:0140789', 'abnormally necrotic roof of mouth', 0.44594594594594594, 7.312692920701687, 1.8058421198805104, 'UPHENO:0076800', 'abnormal mouth morphology'),
(55098, 'HP:0000215', 'Thick upper lip vermilion', 'XPO:0130701', 'increased size of the upper jaw', 0.41379310344827586, 8.81758714901448, 1.9101457408575757, 'UPHENO:0087585', 'abnormal midface morphology'),
(55099, 'HP:0000215', 'Thick upper lip vermilion', 'XPO:0141311', 'abnormal roof of mouth morphology', 0.4782608695652174, 7.312692920701687, 1.8701269676463677, 'UPHENO:0076800', 'abnormal mouth morphology'),
(55100, 'HP:0000215', 'Thick upper lip vermilion', 'XPO:0131611', 'increased size of the roof of mouth', 0.4342105263157895, 7.312692920701687, 1.7819226251113227, 'UPHENO:0076800', 'abnormal mouth morphology'),
(55101, 'HP:0000215', 'Thick upper lip vermilion', 'XPO:0140639', 'abnormally necrotic upper jaw', 0.4235294117647059, 8.81758714901448, 1.932487386351107, 'UPHENO:0087585', 'abnormal midface morphology'),
(55102, 'HP:0000215', 'Thick upper lip vermilion', 'XPO:0131573', 'decreased size of the roof of mouth', 0.4342105263157895, 7.312692920701687, 1.7819226251113227, 'UPHENO:0076800', 'abnormal mouth morphology'),
(55103, 'HP:0000215', 'Thick upper lip vermilion', 'XPO:0115558', 'abnormally incomplete structure of mouth', 0.4925373134328358, 7.312692920701687, 1.8978340615348135, 'UPHENO:0076800', 'abnormal mouth morphology'),
(55104, 'HP:0000215', 'Thick upper lip vermilion', 'XPO:0130628', 'increased size of the oral cavity', 0.49295774647887325, 7.884497199543557, 1.971477611236298, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(55105, 'HP:0000215', 'Thick upper lip vermilion', 'XPO:0101659', 'abnormal lower jaw morphology', 0.425, 7.312692920701687, 1.7629221455578283, 'UPHENO:0076800', 'abnormal mouth morphology'),
(55106, 'HP:0000215', 'Thick upper lip vermilion', 'XPO:0126089', 'absent tongue', 0.4583333333333333, 7.884497199543557, 1.9009807687412648, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(55107, 'HP:0000215', 'Thick upper lip vermilion', 'XPO:0103096', 'abnormal oral cavity morphology', 0.5303030303030303, 7.884497199543557, 2.044791617092975, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(55108, 'HP:0000215', 'Thick upper lip vermilion', 'XPO:0103735', 'increased size of the mouth', 0.4666666666666667, 7.884497199543557, 1.9181845652735452, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(55109, 'HP:0000215', 'Thick upper lip vermilion', 'XPO:0129152', 'decreased size of the oral cavity', 0.49295774647887325, 7.884497199543557, 1.971477611236298, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(55110, 'HP:0000215', 'Thick upper lip vermilion', 'XPO:0102960', 'abnormal oral epithelium morphology', 0.44, 7.312692920701687, 1.7937627728071353, 'UPHENO:0076800', 'abnormal mouth morphology'),
(55111, 'HP:0000215', 'Thick upper lip vermilion', 'XPO:0101567', 'abnormal tongue', 0.5333333333333333, 7.884497199543557, 2.0506255565290066, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(55112, 'HP:0000215', 'Thick upper lip vermilion', 'XPO:0127750', 'abnormally localised tongue', 0.4714285714285714, 7.884497199543557, 1.9279463818305196, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(55113, 'HP:0000215', 'Thick upper lip vermilion', 'XPO:0103828', 'decreased width of the mouth', 0.4375, 7.884497199543557, 1.8572742190641387, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(55114, 'HP:0000215', 'Thick upper lip vermilion', 'XPO:0115393', 'abnormally decreased volume of oral cavity', 0.4794520547945205, 7.884497199543557, 1.9442835141364547, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(55115, 'HP:0000215', 'Thick upper lip vermilion', 'XPO:0101816', 'abnormal tooth morphology', 0.4117647058823529, 7.884497199543557, 1.8018206543383524, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(55116, 'HP:0000215', 'Thick upper lip vermilion', 'XPO:0141830', 'increased width of mouth', 0.4375, 7.884497199543557, 1.8572742190641387, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(55117, 'HP:0000215', 'Thick upper lip vermilion', 'XPO:0102279', 'abnormal mouth morphology', 0.5, 7.312692920701687, 1.9121575406725366, 'UPHENO:0076800', 'abnormal mouth morphology'),
(55118, 'HP:0000215', 'Thick upper lip vermilion', 'XPO:0129585', 'increased size of the tongue', 0.4166666666666667, 7.884497199543557, 1.812514045870123, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(55119, 'HP:0000215', 'Thick upper lip vermilion', 'XPO:0103138', 'abnormal upper jaw morphology', 0.45, 8.81758714901448, 1.9919624035248547, 'UPHENO:0087585', 'abnormal midface morphology'),
(55120, 'HP:0000215', 'Thick upper lip vermilion', 'XPO:0141009', 'abnormally necrotic oral epithelium', 0.4024390243902439, 7.312692920701687, 1.7154920590526295, 'UPHENO:0076800', 'abnormal mouth morphology'),
(55121, 'HP:0003328', 'Abnormal hairshaft morphology', 'XPO:0107346', 'abnormal animal-vegetal axis morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(55122, 'HP:0003328', 'Abnormal hairshaft morphology', 'XPO:0102773', 'abnormal Keller explant morphology', 0.43333333333333335, 2.786899518863159, 1.0989342374200721, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(55123, 'HP:0003328', 'Abnormal hairshaft morphology', 'XPO:0102139', 'abnormal skin morphology', 0.4418604651162791, 6.8660902472206855, 1.741796150577696, 'HP:0000951', 'Abnormality of the skin'),
(55124, 'HP:0003328', 'Abnormal hairshaft morphology', 'XPO:0102386', 'abnormal electrically active cell morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(55125, 'HP:0003328', 'Abnormal hairshaft morphology', 'XPO:0141277', 'abnormal actin cytoskeleton morphology', 0.4166666666666667, 2.786899518863159, 1.0775936770692605, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(55126, 'HP:0003328', 'Abnormal hairshaft morphology', 'XPO:0141285', 'abnormal cortical actin cytoskeleton morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(55127, 'HP:0003328', 'Abnormal hairshaft morphology', 'XPO:0141505', 'abnormal tadpole morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(55128, 'HP:0003328', 'Abnormal hairshaft morphology', 'XPO:0102588', 'abnormal centrosome morphology', 0.4166666666666667, 2.786899518863159, 1.0775936770692605, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(55129, 'HP:0003328', 'Abnormal hairshaft morphology', 'XPO:0101095', 'abnormal skin seromucous gland', 0.40540540540540543, 6.8660902472206855, 1.6683974647021622, 'HP:0000951', 'Abnormality of the skin'),
(55130, 'HP:0003328', 'Abnormal hairshaft morphology', 'XPO:0102539', 'abnormal cytoplasm morphology', 0.4166666666666667, 2.786899518863159, 1.0775936770692605, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(55131, 'HP:0003328', 'Abnormal hairshaft morphology', 'XPO:0141296', 'abnormal adherens junction morphology', 0.4166666666666667, 2.786899518863159, 1.0775936770692605, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(55132, 'HP:0003328', 'Abnormal hairshaft morphology', 'XPO:0102742', 'abnormal cell-free extract morphology', 0.43333333333333335, 2.786899518863159, 1.0989342374200721, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(55133, 'HP:0003328', 'Abnormal hairshaft morphology', 'XPO:0101976', 'abnormal portion of organism substance morphology', 0.4642857142857143, 2.786899518863159, 1.1375050038386183, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(55134, 'HP:0003328', 'Abnormal hairshaft morphology', 'XPO:0102181', 'abnormal mitotic cell morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(55135, 'HP:0003328', 'Abnormal hairshaft morphology', 'XPO:0101713', 'abnormal anatomical entity in vitro morphology', 0.4642857142857143, 2.786899518863159, 1.1375050038386183, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(55136, 'HP:0003328', 'Abnormal hairshaft morphology', 'XPO:0129582', 'increased size of the portion of organism substance', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(55137, 'HP:0003328', 'Abnormal hairshaft morphology', 'XPO:0102958', 'abnormal cementoblast morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(55138, 'HP:0003328', 'Abnormal hairshaft morphology', 'XPO:0128502', 'decreased size of the anatomical line', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(55139, 'HP:0003328', 'Abnormal hairshaft morphology', 'XPO:0102615', 'abnormal skin gland morphology', 0.4418604651162791, 6.8660902472206855, 1.741796150577696, 'HP:0000951', 'Abnormality of the skin'),
(55140, 'HP:0003328', 'Abnormal hairshaft morphology', 'XPO:0103145', 'abnormal basal body morphology', 0.4166666666666667, 2.786899518863159, 1.0775936770692605, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(55141, 'HP:0003328', 'Abnormal hairshaft morphology', 'XPO:0102347', 'abnormal ciliated cell morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(55142, 'HP:0003328', 'Abnormal hairshaft morphology', 'XPO:0102113', 'abnormal anatomical line morphology', 0.4642857142857143, 2.786899518863159, 1.1375050038386183, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(55143, 'HP:0003328', 'Abnormal hairshaft morphology', 'XPO:0102910', 'abnormal pigment cell morphology', 0.41304347826086957, 6.8660902472206855, 1.6840409133287308, 'HP:0000951', 'Abnormality of the skin'),
(55144, 'HP:0003328', 'Abnormal hairshaft morphology', 'XPO:0102929', 'abnormal barrier cell morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(55145, 'HP:0003328', 'Abnormal hairshaft morphology', 'XPO:0101917', 'abnormal progenitor cell morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(55146, 'HP:0003328', 'Abnormal hairshaft morphology', 'XPO:0103104', 'abnormal zygote cortex morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(55147, 'HP:0003328', 'Abnormal hairshaft morphology', 'XPO:0115510', 'abnormal degeneration of whole organism', 0.41935483870967744, 2.786899518863159, 1.0810641970914296, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(55148, 'HP:0003328', 'Abnormal hairshaft morphology', 'XPO:0103179', 'abnormal lampbrush chromosome morphology', 0.4166666666666667, 2.786899518863159, 1.0775936770692605, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(55149, 'HP:0003328', 'Abnormal hairshaft morphology', 'XPO:0101969', 'abnormal zygote morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(55150, 'HP:0003328', 'Abnormal hairshaft morphology', 'XPO:0102741', 'abnormal egg cell-free extract morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(55151, 'HP:0003328', 'Abnormal hairshaft morphology', 'XPO:0128007', 'decreased size of the anatomical structure', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(55152, 'HP:0003328', 'Abnormal hairshaft morphology', 'XPO:0102177', 'abnormal male organism morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(55153, 'HP:0003328', 'Abnormal hairshaft morphology', 'XPO:0102896', 'abnormal mitotic spindle morphology', 0.4166666666666667, 2.786899518863159, 1.0775936770692605, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(55154, 'HP:0003328', 'Abnormal hairshaft morphology', 'XPO:0102024', 'abnormal cilium morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(55155, 'HP:0003328', 'Abnormal hairshaft morphology', 'XPO:0102840', 'abnormal stratum spongiosum morphology', 0.41304347826086957, 6.8660902472206855, 1.6840409133287308, 'HP:0000951', 'Abnormality of the skin'),
(55156, 'HP:0003328', 'Abnormal hairshaft morphology', 'XPO:0102703', 'abnormal endoplasmic reticulum morphology', 0.4166666666666667, 2.786899518863159, 1.0775936770692605, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(55157, 'HP:0003328', 'Abnormal hairshaft morphology', 'XPO:0103005', 'abnormal oxygen accumulating cell morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(55158, 'HP:0003328', 'Abnormal hairshaft morphology', 'XPO:0102965', 'abnormal barrier epithelial cell morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(55159, 'HP:0003328', 'Abnormal hairshaft morphology', 'XPO:0107399', 'abnormal filopodium morphology', 0.4166666666666667, 2.786899518863159, 1.0775936770692605, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(55160, 'HP:0003328', 'Abnormal hairshaft morphology', 'XPO:0102176', 'abnormal neuromast support cell morphology', 0.41304347826086957, 6.8660902472206855, 1.6840409133287308, 'HP:0000951', 'Abnormality of the skin'),
(55161, 'HP:0003328', 'Abnormal hairshaft morphology', 'XPO:0141316', 'abnormal anatomical region morphology', 0.43333333333333335, 2.786899518863159, 1.0989342374200721, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(55162, 'HP:0003328', 'Abnormal hairshaft morphology', 'XPO:0129982', 'increased size of the anatomical line', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(55163, 'HP:0003328', 'Abnormal hairshaft morphology', 'XPO:0107348', 'abnormal dorsal-ventral axis morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(55164, 'HP:0003328', 'Abnormal hairshaft morphology', 'XPO:0140269', 'abnormally necrotic anatomical line', 0.43333333333333335, 2.786899518863159, 1.0989342374200721, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(55165, 'HP:0003328', 'Abnormal hairshaft morphology', 'XPO:0102205', 'abnormal extraembryonic structure morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(55166, 'HP:0003328', 'Abnormal hairshaft morphology', 'XPO:0107357', 'abnormal proximal-distal axis morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(55167, 'HP:0003328', 'Abnormal hairshaft morphology', 'XPO:0107345', 'abnormal anatomical axis morphology', 0.43333333333333335, 2.786899518863159, 1.0989342374200721, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(55168, 'HP:0003328', 'Abnormal hairshaft morphology', 'XPO:0101716', 'abnormal anatomical group morphology', 0.41935483870967744, 2.786899518863159, 1.0810641970914296, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(55169, 'HP:0003328', 'Abnormal hairshaft morphology', 'XPO:0102636', 'abnormal acid secreting cell morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(55170, 'HP:0003328', 'Abnormal hairshaft morphology', 'XPO:0102133', 'abnormal urogenital system morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(55171, 'HP:0003328', 'Abnormal hairshaft morphology', 'XPO:0128102', 'decreased size of the portion of organism substance', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(55172, 'HP:0003328', 'Abnormal hairshaft morphology', 'XPO:0102601', 'abnormal disaggregated/reaggregated ectoderm treated with activin morphology', 0.43333333333333335, 2.786899518863159, 1.0989342374200721, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(55173, 'HP:0003328', 'Abnormal hairshaft morphology', 'XPO:0129487', 'increased size of the anatomical structure', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(55174, 'HP:0003328', 'Abnormal hairshaft morphology', 'XPO:0100983', 'abnormal skin gland', 0.4166666666666667, 6.8660902472206855, 1.6914109306558096, 'HP:0000951', 'Abnormality of the skin'),
(55175, 'HP:0003328', 'Abnormal hairshaft morphology', 'XPO:0103202', 'abnormal forelimb region morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(55176, 'HP:0003328', 'Abnormal hairshaft morphology', 'XPO:0100507', 'abnormal skin', 0.42857142857142855, 6.8660902472206855, 1.7154037734456928, 'HP:0000951', 'Abnormality of the skin'),
(55177, 'HP:0003328', 'Abnormal hairshaft morphology', 'XPO:0102055', 'abnormal process morphology', 0.41935483870967744, 2.786899518863159, 1.0810641970914296, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(55178, 'HP:0003328', 'Abnormal hairshaft morphology', 'XPO:0102178', 'abnormal whole organism morphology', 0.43333333333333335, 2.786899518863159, 1.0989342374200721, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(55179, 'HP:0003328', 'Abnormal hairshaft morphology', 'XPO:0141299', 'abnormal actin filament morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(55180, 'HP:0003328', 'Abnormal hairshaft morphology', 'XPO:0102336', 'abnormal Merkel cell morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(55181, 'HP:0003328', 'Abnormal hairshaft morphology', 'XPO:0142064', 'abnormal desmosome morphology', 0.4166666666666667, 2.786899518863159, 1.0775936770692605, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(55182, 'HP:0003328', 'Abnormal hairshaft morphology', 'XPO:0102693', 'abnormal plasma membrane morphology', 0.4166666666666667, 2.786899518863159, 1.0775936770692605, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(55183, 'HP:0003328', 'Abnormal hairshaft morphology', 'XPO:0102360', 'abnormal cell condensation morphology', 0.41935483870967744, 2.786899518863159, 1.0810641970914296, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(55184, 'HP:0003328', 'Abnormal hairshaft morphology', 'XPO:0102727', 'abnormal skin seromucous gland morphology', 0.4222222222222222, 6.8660902472206855, 1.7026496651278105, 'HP:0000951', 'Abnormality of the skin'),
(55185, 'HP:0003328', 'Abnormal hairshaft morphology', 'XPO:0102873', 'abnormal nucleate erythrocyte morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(55186, 'HP:0003328', 'Abnormal hairshaft morphology', 'XPO:0103043', 'abnormal marginal zone (sensu neural) morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(55187, 'HP:0003328', 'Abnormal hairshaft morphology', 'XPO:0139841', 'abnormally necrotic anatomical region', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(55188, 'HP:0003328', 'Abnormal hairshaft morphology', 'XPO:0102434', 'abnormal exocrine cell morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(55189, 'HP:0003328', 'Abnormal hairshaft morphology', 'XPO:0103080', 'abnormal myelin accumulating cell morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(55190, 'HP:0003328', 'Abnormal hairshaft morphology', 'XPO:0101921', 'abnormal chondroblast morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(55191, 'HP:0003328', 'Abnormal hairshaft morphology', 'XPO:0102165', 'abnormal melanoblast morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(55192, 'HP:0003328', 'Abnormal hairshaft morphology', 'XPO:0102526', 'abnormal nucleus morphology', 0.4166666666666667, 2.786899518863159, 1.0775936770692605, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(55193, 'HP:0003328', 'Abnormal hairshaft morphology', 'XPO:0101642', 'abnormal multicellular anatomical structure morphology', 0.41935483870967744, 2.786899518863159, 1.0810641970914296, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(55194, 'HP:0003328', 'Abnormal hairshaft morphology', 'XPO:0102520', 'abnormal microtubule morphology', 0.4166666666666667, 2.786899518863159, 1.0775936770692605, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(55195, 'HP:0003328', 'Abnormal hairshaft morphology', 'XPO:0102789', 'abnormal female organism morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(55196, 'HP:0003328', 'Abnormal hairshaft morphology', 'XPO:0102945', 'abnormal Eberth-Kastschenko layer morphology', 0.41304347826086957, 6.8660902472206855, 1.6840409133287308, 'HP:0000951', 'Abnormality of the skin'),
(55197, 'HP:0003328', 'Abnormal hairshaft morphology', 'XPO:0102626', 'abnormal granular gland morphology', 0.4222222222222222, 6.8660902472206855, 1.7026496651278105, 'HP:0000951', 'Abnormality of the skin'),
(55198, 'HP:0003328', 'Abnormal hairshaft morphology', 'XPO:0102285', 'abnormal myoblast morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(55199, 'HP:0003328', 'Abnormal hairshaft morphology', 'XPO:0102275', 'abnormal thoracic region morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(55200, 'HP:0003328', 'Abnormal hairshaft morphology', 'XPO:0101871', 'abnormal acellular anatomical structure morphology', 0.41935483870967744, 2.786899518863159, 1.0810641970914296, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(55201, 'HP:0003328', 'Abnormal hairshaft morphology', 'XPO:0102323', 'abnormal keratin accumulating cell morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(55202, 'HP:0003328', 'Abnormal hairshaft morphology', 'XPO:0102353', 'abnormal centromere morphology', 0.4166666666666667, 2.786899518863159, 1.0775936770692605, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(55203, 'HP:0003328', 'Abnormal hairshaft morphology', 'XPO:0102852', 'abnormal centriole morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(55204, 'HP:0003328', 'Abnormal hairshaft morphology', 'XPO:0102561', 'abnormal dermis morphology', 0.4318181818181818, 6.8660902472206855, 1.7218892550783826, 'HP:0000951', 'Abnormality of the skin'),
(55205, 'HP:0003328', 'Abnormal hairshaft morphology', 'XPO:0102979', 'abnormal hindlimb region morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(55206, 'HP:0003328', 'Abnormal hairshaft morphology', 'XPO:0101804', 'abnormal stem cell morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(55207, 'HP:0003328', 'Abnormal hairshaft morphology', 'XPO:0103093', 'abnormal sperm entry point morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(55208, 'HP:0003328', 'Abnormal hairshaft morphology', 'XPO:0101638', 'abnormal anatomical structure morphology', 0.4642857142857143, 2.786899518863159, 1.1375050038386183, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(55209, 'HP:0003328', 'Abnormal hairshaft morphology', 'XPO:0139718', 'abnormally necrotic anatomical structure', 0.43333333333333335, 2.786899518863159, 1.0989342374200721, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(55210, 'HP:0003328', 'Abnormal hairshaft morphology', 'XPO:0102886', 'abnormal stratum compactum morphology', 0.41304347826086957, 6.8660902472206855, 1.6840409133287308, 'HP:0000951', 'Abnormality of the skin'),
(55211, 'HP:0003328', 'Abnormal hairshaft morphology', 'XPO:0102764', 'abnormal apoptotic cell morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(55212, 'HP:0003328', 'Abnormal hairshaft morphology', 'XPO:0103099', 'abnormal alkali secreting cell morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(55213, 'HP:0003328', 'Abnormal hairshaft morphology', 'XPO:0102109', 'abnormal pericyte morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(55214, 'HP:0003328', 'Abnormal hairshaft morphology', 'XPO:0102423', 'abnormal multiciliated cell precursor morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(55215, 'HP:0003328', 'Abnormal hairshaft morphology', 'XPO:0107359', 'abnormal axial region morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(55216, 'HP:0003328', 'Abnormal hairshaft morphology', 'XPO:0140144', 'abnormally necrotic portion of organism substance', 0.43333333333333335, 2.786899518863159, 1.0989342374200721, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(55217, 'HP:0003328', 'Abnormal hairshaft morphology', 'XPO:0103167', 'abnormal absorptive cell morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(55218, 'HP:0003328', 'Abnormal hairshaft morphology', 'XPO:0107347', 'abnormal anterior-posterior axis morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(55219, 'HP:0003328', 'Abnormal hairshaft morphology', 'XPO:0101636', 'abnormal cell morphology', 0.42857142857142855, 2.786899518863159, 1.092879457252359, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(55220, 'HP:0003328', 'Abnormal hairshaft morphology', 'XPO:0101658', 'abnormal germ cell morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(55221, 'HP:0003328', 'Abnormal hairshaft morphology', 'XPO:0103147', 'abnormal neuromast mantle cell morphology', 0.41304347826086957, 6.8660902472206855, 1.6840409133287308, 'HP:0000951', 'Abnormality of the skin'),
(55222, 'HP:0003328', 'Abnormal hairshaft morphology', 'XPO:0102869', 'abnormal mucus secreting cell morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(55223, 'HP:0003328', 'Abnormal hairshaft morphology', 'XPO:0102356', 'abnormal kinetochore morphology', 0.4166666666666667, 2.786899518863159, 1.0775936770692605, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(55224, 'HP:0003328', 'Abnormal hairshaft morphology', 'XPO:0103201', 'abnormal activin-induced ectoderm morphology', 0.43333333333333335, 2.786899518863159, 1.0989342374200721, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(55225, 'HP:0003328', 'Abnormal hairshaft morphology', 'XPO:0107350', 'abnormal anatomical side morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(55226, 'HP:0003328', 'Abnormal hairshaft morphology', 'XPO:0100994', 'abnormal granular gland', 0.40540540540540543, 6.8660902472206855, 1.6683974647021622, 'HP:0000951', 'Abnormality of the skin'),
(55227, 'HP:0003328', 'Abnormal hairshaft morphology', 'XPO:0101890', 'abnormal organ part morphology', 0.43333333333333335, 2.786899518863159, 1.0989342374200721, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(55228, 'HP:0003328', 'Abnormal hairshaft morphology', 'XPO:0107349', 'abnormal left-right axis morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(55229, 'HP:0003328', 'Abnormal hairshaft morphology', 'XPO:0101740', 'abnormal cell part morphology', 0.4411764705882353, 2.786899518863159, 1.1088347458553505, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(55230, 'HP:0003328', 'Abnormal hairshaft morphology', 'XPO:0100929', 'abnormal dermis', 0.40540540540540543, 6.8660902472206855, 1.6683974647021622, 'HP:0000951', 'Abnormality of the skin'),
(55231, 'HP:0003328', 'Abnormal hairshaft morphology', 'XPO:0103067', 'abnormal paracrine cell morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(55232, 'HP:0003328', 'Abnormal hairshaft morphology', 'XPO:0102832', 'abnormal joint region morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(55233, 'HP:0003328', 'Abnormal hairshaft morphology', 'XPO:0101694', 'abnormal anatomical space morphology', 0.43333333333333335, 2.786899518863159, 1.0989342374200721, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(55234, 'HP:0025038', 'Intratesticular abscess', 'XPO:0130391', 'increased size of the seminiferous tubule', 0.6209677419354839, 10.7042552034261, 2.578177104617264, 'HP:0000035', 'Abnormal testis morphology'),
(55235, 'HP:0025038', 'Intratesticular abscess', 'XPO:0102046', 'abnormal testis morphology', 0.7129629629629629, 10.7042552034261, 2.762559955212988, 'HP:0000035', 'Abnormal testis morphology'),
(55236, 'HP:0025038', 'Intratesticular abscess', 'XPO:0128913', 'decreased size of the seminiferous tubule', 0.6260162601626016, 10.7042552034261, 2.5886362838905885, 'HP:0000035', 'Abnormal testis morphology'),
(55237, 'HP:0025038', 'Intratesticular abscess', 'XPO:0139754', 'abnormally necrotic testis', 0.6637931034482759, 10.7042552034261, 2.6655976406023036, 'HP:0000035', 'Abnormal testis morphology'),
(55238, 'HP:0025038', 'Intratesticular abscess', 'XPO:0128559', 'decreased size of the testis', 0.5833333333333334, 10.7042552034261, 2.4988294997188634, 'HP:0000035', 'Abnormal testis morphology'),
(55239, 'HP:0025038', 'Intratesticular abscess', 'XPO:0130039', 'increased size of the testis', 0.6311475409836066, 10.7042552034261, 2.599223797540981, 'HP:0000035', 'Abnormal testis morphology'),
(55240, 'HP:0010853', 'EEG with periodic lateralized epileptiform discharges', 'XPO:0100032', 'abnormal nervous system', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(55241, 'HP:0012176', 'Abnormal natural killer cell morphology', 'XPO:0139951', 'abnormally necrotic lymphocyte', 0.44, 6.786309419308587, 1.7279977269938114, 'UPHENO:0087123', 'abnormal immune system morphology'),
(55242, 'HP:0012176', 'Abnormal natural killer cell morphology', 'XPO:0102636', 'abnormal acid secreting cell morphology', 0.4418604651162791, 5.43643956286526, 1.5498863551319448, 'HP:0025461', 'Abnormal cell morphology'),
(55243, 'HP:0012176', 'Abnormal natural killer cell morphology', 'XPO:0103067', 'abnormal paracrine cell morphology', 0.4418604651162791, 5.43643956286526, 1.5498863551319448, 'HP:0025461', 'Abnormal cell morphology'),
(55244, 'HP:0012176', 'Abnormal natural killer cell morphology', 'XPO:0102165', 'abnormal melanoblast morphology', 0.4418604651162791, 5.43643956286526, 1.5498863551319448, 'HP:0025461', 'Abnormal cell morphology'),
(55245, 'HP:0012176', 'Abnormal natural killer cell morphology', 'XPO:0101740', 'abnormal cell part morphology', 0.40476190476190477, 3.6715585125471644, 1.219059890646631, 'UPHENO:0086172', 'abnormal cell'),
(55246, 'HP:0012176', 'Abnormal natural killer cell morphology', 'XPO:0140709', 'abnormally necrotic acid secreting cell', 0.40425531914893614, 5.43643956286526, 1.4824674062251753, 'HP:0025461', 'Abnormal cell morphology'),
(55247, 'HP:0012176', 'Abnormal natural killer cell morphology', 'XPO:0103130', 'abnormal stage II oocyte morphology', 0.40425531914893614, 5.43643956286526, 1.4824674062251753, 'HP:0025461', 'Abnormal cell morphology'),
(55248, 'HP:0012176', 'Abnormal natural killer cell morphology', 'XPO:0139839', 'abnormally necrotic progenitor cell', 0.40425531914893614, 5.43643956286526, 1.4824674062251753, 'HP:0025461', 'Abnormal cell morphology'),
(55249, 'HP:0012176', 'Abnormal natural killer cell morphology', 'XPO:0139717', 'abnormally necrotic cell', 0.4318181818181818, 5.43643956286526, 1.532172786470543, 'HP:0025461', 'Abnormal cell morphology'),
(55250, 'HP:0012176', 'Abnormal natural killer cell morphology', 'XPO:0141146', 'abnormally necrotic oxygen accumulating cell', 0.40425531914893614, 5.43643956286526, 1.4824674062251753, 'HP:0025461', 'Abnormal cell morphology'),
(55251, 'HP:0012176', 'Abnormal natural killer cell morphology', 'XPO:0102434', 'abnormal exocrine cell morphology', 0.4418604651162791, 5.43643956286526, 1.5498863551319448, 'HP:0025461', 'Abnormal cell morphology'),
(55252, 'HP:0012176', 'Abnormal natural killer cell morphology', 'XPO:0140733', 'abnormally necrotic T cell', 0.41509433962264153, 6.786309419308587, 1.6783797624145764, 'UPHENO:0087123', 'abnormal immune system morphology'),
(55253, 'HP:0012176', 'Abnormal natural killer cell morphology', 'XPO:0102323', 'abnormal keratin accumulating cell morphology', 0.4418604651162791, 5.43643956286526, 1.5498863551319448, 'HP:0025461', 'Abnormal cell morphology'),
(55254, 'HP:0012176', 'Abnormal natural killer cell morphology', 'XPO:0102080', 'abnormal thymocyte morphology', 0.4788732394366197, 8.504690711543915, 2.0180854271917146, 'UPHENO:0084888', 'abnormal lymphocyte morphology'),
(55255, 'HP:0012176', 'Abnormal natural killer cell morphology', 'XPO:0102446', 'abnormal natural killer cell morphology', 0.44, 6.786309419308587, 1.7279977269938114, 'UPHENO:0087123', 'abnormal immune system morphology'),
(55256, 'HP:0012176', 'Abnormal natural killer cell morphology', 'XPO:0102258', 'abnormal primordial germ cell morphology', 0.4222222222222222, 5.43643956286526, 1.5150530001322648, 'HP:0025461', 'Abnormal cell morphology'),
(55257, 'HP:0012176', 'Abnormal natural killer cell morphology', 'XPO:0107371', 'abnormal migrating myoblast morphology', 0.4222222222222222, 5.43643956286526, 1.5150530001322648, 'HP:0025461', 'Abnormal cell morphology'),
(55258, 'HP:0012176', 'Abnormal natural killer cell morphology', 'XPO:0140868', 'abnormally necrotic chondroblast', 0.40425531914893614, 5.43643956286526, 1.4824674062251753, 'HP:0025461', 'Abnormal cell morphology'),
(55259, 'HP:0012176', 'Abnormal natural killer cell morphology', 'XPO:0102531', 'abnormal secondary spermatogonium morphology', 0.4222222222222222, 5.43643956286526, 1.5150530001322648, 'HP:0025461', 'Abnormal cell morphology'),
(55260, 'HP:0012176', 'Abnormal natural killer cell morphology', 'XPO:0102109', 'abnormal pericyte morphology', 0.4418604651162791, 5.43643956286526, 1.5498863551319448, 'HP:0025461', 'Abnormal cell morphology'),
(55261, 'HP:0012176', 'Abnormal natural killer cell morphology', 'XPO:0129956', 'increased size of the thymocyte', 0.40476190476190477, 8.504690711543915, 1.8553637950050104, 'UPHENO:0084888', 'abnormal lymphocyte morphology'),
(55262, 'HP:0012176', 'Abnormal natural killer cell morphology', 'XPO:0102423', 'abnormal multiciliated cell precursor morphology', 0.4418604651162791, 5.43643956286526, 1.5498863551319448, 'HP:0025461', 'Abnormal cell morphology'),
(55263, 'HP:0012176', 'Abnormal natural killer cell morphology', 'XPO:0140278', 'abnormally necrotic Merkel cell', 0.40425531914893614, 5.43643956286526, 1.4824674062251753, 'HP:0025461', 'Abnormal cell morphology'),
(55264, 'HP:0012176', 'Abnormal natural killer cell morphology', 'XPO:0101940', 'abnormal early embryonic cell morphology', 0.4222222222222222, 5.43643956286526, 1.5150530001322648, 'HP:0025461', 'Abnormal cell morphology'),
(55265, 'HP:0012176', 'Abnormal natural killer cell morphology', 'XPO:0140589', 'abnormally necrotic keratin accumulating cell', 0.40425531914893614, 5.43643956286526, 1.4824674062251753, 'HP:0025461', 'Abnormal cell morphology'),
(55266, 'HP:0012176', 'Abnormal natural killer cell morphology', 'XPO:0107341', 'abnormal neutrophil morphology', 0.41379310344827586, 6.786309419308587, 1.6757470082252772, 'UPHENO:0087123', 'abnormal immune system morphology'),
(55267, 'HP:0012176', 'Abnormal natural killer cell morphology', 'XPO:0141503', 'abnormal lymphoblast morphology', 0.4782608695652174, 6.786309419308587, 1.8015621676803582, 'UPHENO:0087123', 'abnormal immune system morphology'),
(55268, 'HP:0012176', 'Abnormal natural killer cell morphology', 'XPO:0141007', 'abnormally necrotic electrically active cell', 0.40425531914893614, 5.43643956286526, 1.4824674062251753, 'HP:0025461', 'Abnormal cell morphology'),
(55269, 'HP:0012176', 'Abnormal natural killer cell morphology', 'XPO:0102860', 'abnormal mesenchymal stem cell morphology', 0.4222222222222222, 5.43643956286526, 1.5150530001322648, 'HP:0025461', 'Abnormal cell morphology'),
(55270, 'HP:0012176', 'Abnormal natural killer cell morphology', 'XPO:0141065', 'abnormally necrotic paracrine cell', 0.40425531914893614, 5.43643956286526, 1.4824674062251753, 'HP:0025461', 'Abnormal cell morphology'),
(55271, 'HP:0012176', 'Abnormal natural killer cell morphology', 'XPO:0102181', 'abnormal mitotic cell morphology', 0.4418604651162791, 5.43643956286526, 1.5498863551319448, 'HP:0025461', 'Abnormal cell morphology'),
(55272, 'HP:0012176', 'Abnormal natural killer cell morphology', 'XPO:0102873', 'abnormal nucleate erythrocyte morphology', 0.4418604651162791, 5.43643956286526, 1.5498863551319448, 'HP:0025461', 'Abnormal cell morphology'),
(55273, 'HP:0012176', 'Abnormal natural killer cell morphology', 'XPO:0101636', 'abnormal cell morphology', 0.4634146341463415, 5.43643956286526, 1.587238372483447, 'HP:0025461', 'Abnormal cell morphology'),
(55274, 'HP:0012176', 'Abnormal natural killer cell morphology', 'XPO:0140010', 'abnormally necrotic zygote', 0.40425531914893614, 5.43643956286526, 1.4824674062251753, 'HP:0025461', 'Abnormal cell morphology'),
(55275, 'HP:0012176', 'Abnormal natural killer cell morphology', 'XPO:0102872', 'abnormal ciliated non-epidermal cell morphology', 0.4222222222222222, 5.43643956286526, 1.5150530001322648, 'HP:0025461', 'Abnormal cell morphology'),
(55276, 'HP:0012176', 'Abnormal natural killer cell morphology', 'XPO:0102745', 'abnormal stage IV oocyte morphology', 0.40425531914893614, 5.43643956286526, 1.4824674062251753, 'HP:0025461', 'Abnormal cell morphology'),
(55277, 'HP:0012176', 'Abnormal natural killer cell morphology', 'XPO:0102347', 'abnormal ciliated cell morphology', 0.4418604651162791, 5.43643956286526, 1.5498863551319448, 'HP:0025461', 'Abnormal cell morphology'),
(55278, 'HP:0012176', 'Abnormal natural killer cell morphology', 'XPO:0102306', 'abnormal secondary oogonium morphology', 0.4222222222222222, 5.43643956286526, 1.5150530001322648, 'HP:0025461', 'Abnormal cell morphology'),
(55279, 'HP:0012176', 'Abnormal natural killer cell morphology', 'XPO:0101917', 'abnormal progenitor cell morphology', 0.4418604651162791, 5.43643956286526, 1.5498863551319448, 'HP:0025461', 'Abnormal cell morphology'),
(55280, 'HP:0012176', 'Abnormal natural killer cell morphology', 'XPO:0141147', 'abnormally necrotic alkali secreting cell', 0.40425531914893614, 5.43643956286526, 1.4824674062251753, 'HP:0025461', 'Abnormal cell morphology'),
(55281, 'HP:0012176', 'Abnormal natural killer cell morphology', 'XPO:0140803', 'abnormally necrotic pericyte', 0.40425531914893614, 5.43643956286526, 1.4824674062251753, 'HP:0025461', 'Abnormal cell morphology'),
(55282, 'HP:0012176', 'Abnormal natural killer cell morphology', 'XPO:0101657', 'abnormal oocyte morphology', 0.4222222222222222, 5.43643956286526, 1.5150530001322648, 'HP:0025461', 'Abnormal cell morphology'),
(55283, 'HP:0012176', 'Abnormal natural killer cell morphology', 'XPO:0139759', 'abnormally necrotic germ cell', 0.40425531914893614, 5.43643956286526, 1.4824674062251753, 'HP:0025461', 'Abnormal cell morphology'),
(55284, 'HP:0012176', 'Abnormal natural killer cell morphology', 'XPO:0102764', 'abnormal apoptotic cell morphology', 0.4418604651162791, 5.43643956286526, 1.5498863551319448, 'HP:0025461', 'Abnormal cell morphology'),
(55285, 'HP:0012176', 'Abnormal natural killer cell morphology', 'XPO:0102534', 'abnormal spermatocyte morphology', 0.4222222222222222, 5.43643956286526, 1.5150530001322648, 'HP:0025461', 'Abnormal cell morphology'),
(55286, 'HP:0012176', 'Abnormal natural killer cell morphology', 'XPO:0102958', 'abnormal cementoblast morphology', 0.4418604651162791, 5.43643956286526, 1.5498863551319448, 'HP:0025461', 'Abnormal cell morphology'),
(55287, 'HP:0012176', 'Abnormal natural killer cell morphology', 'XPO:0101969', 'abnormal zygote morphology', 0.4418604651162791, 5.43643956286526, 1.5498863551319448, 'HP:0025461', 'Abnormal cell morphology'),
(55288, 'HP:0012176', 'Abnormal natural killer cell morphology', 'XPO:0102081', 'abnormal lymphocyte morphology', 0.4782608695652174, 6.786309419308587, 1.8015621676803582, 'UPHENO:0087123', 'abnormal immune system morphology'),
(55289, 'HP:0012176', 'Abnormal natural killer cell morphology', 'XPO:0102848', 'abnormal macrophage morphology', 0.41379310344827586, 6.786309419308587, 1.6757470082252772, 'UPHENO:0087123', 'abnormal immune system morphology'),
(55290, 'HP:0012176', 'Abnormal natural killer cell morphology', 'XPO:0140647', 'abnormally necrotic nucleate erythrocyte', 0.40425531914893614, 5.43643956286526, 1.4824674062251753, 'HP:0025461', 'Abnormal cell morphology'),
(55291, 'HP:0012176', 'Abnormal natural killer cell morphology', 'XPO:0102869', 'abnormal mucus secreting cell morphology', 0.4418604651162791, 5.43643956286526, 1.5498863551319448, 'HP:0025461', 'Abnormal cell morphology'),
(55292, 'HP:0012176', 'Abnormal natural killer cell morphology', 'XPO:0140075', 'abnormally necrotic stem cell', 0.40425531914893614, 5.43643956286526, 1.4824674062251753, 'HP:0025461', 'Abnormal cell morphology'),
(55293, 'HP:0012176', 'Abnormal natural killer cell morphology', 'XPO:0140973', 'abnormally necrotic erythroid cell', 0.4117647058823529, 5.574066539846944, 1.5149930261716527, 'UPHENO:0004459', 'abnormal hematopoietic system'),
(55294, 'HP:0012176', 'Abnormal natural killer cell morphology', 'XPO:0141203', 'abnormally necrotic exocrine cell', 0.40425531914893614, 5.43643956286526, 1.4824674062251753, 'HP:0025461', 'Abnormal cell morphology'),
(55295, 'HP:0012176', 'Abnormal natural killer cell morphology', 'XPO:0103167', 'abnormal absorptive cell morphology', 0.4418604651162791, 5.43643956286526, 1.5498863551319448, 'HP:0025461', 'Abnormal cell morphology'),
(55296, 'HP:0012176', 'Abnormal natural killer cell morphology', 'XPO:0101804', 'abnormal stem cell morphology', 0.4418604651162791, 5.43643956286526, 1.5498863551319448, 'HP:0025461', 'Abnormal cell morphology'),
(55297, 'HP:0012176', 'Abnormal natural killer cell morphology', 'XPO:0140117', 'abnormally necrotic thymocyte', 0.4473684210526316, 8.504690711543915, 1.9505717252037629, 'UPHENO:0084888', 'abnormal lymphocyte morphology'),
(55298, 'HP:0012176', 'Abnormal natural killer cell morphology', 'XPO:0102715', 'abnormal T cell morphology', 0.4583333333333333, 6.786309419308587, 1.7636302949266613, 'UPHENO:0087123', 'abnormal immune system morphology'),
(55299, 'HP:0012176', 'Abnormal natural killer cell morphology', 'XPO:0102069', 'abnormal proepicardium morphology', 0.4222222222222222, 5.43643956286526, 1.5150530001322648, 'HP:0025461', 'Abnormal cell morphology'),
(55300, 'HP:0012176', 'Abnormal natural killer cell morphology', 'XPO:0102386', 'abnormal electrically active cell morphology', 0.4418604651162791, 5.43643956286526, 1.5498863551319448, 'HP:0025461', 'Abnormal cell morphology'),
(55301, 'HP:0012176', 'Abnormal natural killer cell morphology', 'XPO:0102206', 'abnormal gastrula cell morphology', 0.40425531914893614, 5.43643956286526, 1.4824674062251753, 'HP:0025461', 'Abnormal cell morphology'),
(55302, 'HP:0012176', 'Abnormal natural killer cell morphology', 'XPO:0103080', 'abnormal myelin accumulating cell morphology', 0.4418604651162791, 5.43643956286526, 1.5498863551319448, 'HP:0025461', 'Abnormal cell morphology'),
(55303, 'HP:0012176', 'Abnormal natural killer cell morphology', 'XPO:0131005', 'abnormally increased number of thymocyte', 0.40476190476190477, 8.504690711543915, 1.8553637950050104, 'UPHENO:0084888', 'abnormal lymphocyte morphology'),
(55304, 'HP:0012176', 'Abnormal natural killer cell morphology', 'XPO:0101658', 'abnormal germ cell morphology', 0.4418604651162791, 5.43643956286526, 1.5498863551319448, 'HP:0025461', 'Abnormal cell morphology'),
(55305, 'HP:0012176', 'Abnormal natural killer cell morphology', 'XPO:0102965', 'abnormal barrier epithelial cell morphology', 0.4418604651162791, 5.43643956286526, 1.5498863551319448, 'HP:0025461', 'Abnormal cell morphology'),
(55306, 'HP:0012176', 'Abnormal natural killer cell morphology', 'XPO:0103150', 'abnormal B cell morphology', 0.4583333333333333, 6.786309419308587, 1.7636302949266613, 'UPHENO:0087123', 'abnormal immune system morphology'),
(55307, 'HP:0012176', 'Abnormal natural killer cell morphology', 'XPO:0128476', 'decreased size of the thymocyte', 0.40476190476190477, 8.504690711543915, 1.8553637950050104, 'UPHENO:0084888', 'abnormal lymphocyte morphology'),
(55308, 'HP:0012176', 'Abnormal natural killer cell morphology', 'XPO:0102549', 'abnormal stage III oocyte morphology', 0.40425531914893614, 5.43643956286526, 1.4824674062251753, 'HP:0025461', 'Abnormal cell morphology'),
(55309, 'HP:0012176', 'Abnormal natural killer cell morphology', 'XPO:0140533', 'abnormally necrotic myelin accumulating cell', 0.40425531914893614, 5.43643956286526, 1.4824674062251753, 'HP:0025461', 'Abnormal cell morphology'),
(55310, 'HP:0012176', 'Abnormal natural killer cell morphology', 'XPO:0103082', 'abnormal myeloid cell morphology', 0.44680851063829785, 5.574066539846944, 1.5781445969453445, 'HP:0001871', 'Abnormality of blood and blood-forming tissues'),
(55311, 'HP:0012176', 'Abnormal natural killer cell morphology', 'XPO:0103005', 'abnormal oxygen accumulating cell morphology', 0.4418604651162791, 5.43643956286526, 1.5498863551319448, 'HP:0025461', 'Abnormal cell morphology'),
(55312, 'HP:0012176', 'Abnormal natural killer cell morphology', 'XPO:0140919', 'abnormally necrotic cementoblast', 0.40425531914893614, 5.43643956286526, 1.4824674062251753, 'HP:0025461', 'Abnormal cell morphology'),
(55313, 'HP:0012176', 'Abnormal natural killer cell morphology', 'XPO:0141048', 'abnormally necrotic mitotic cell', 0.40425531914893614, 5.43643956286526, 1.4824674062251753, 'HP:0025461', 'Abnormal cell morphology'),
(55314, 'HP:0012176', 'Abnormal natural killer cell morphology', 'XPO:0102147', 'abnormal somatic stem cell morphology', 0.4222222222222222, 5.43643956286526, 1.5150530001322648, 'HP:0025461', 'Abnormal cell morphology'),
(55315, 'HP:0012176', 'Abnormal natural killer cell morphology', 'XPO:0141478', 'abnormally necrotic lymphoblast', 0.44, 6.786309419308587, 1.7279977269938114, 'UPHENO:0087123', 'abnormal immune system morphology'),
(55316, 'HP:0012176', 'Abnormal natural killer cell morphology', 'XPO:0101939', 'abnormal blastomere morphology', 0.40425531914893614, 5.43643956286526, 1.4824674062251753, 'HP:0025461', 'Abnormal cell morphology'),
(55317, 'HP:0012176', 'Abnormal natural killer cell morphology', 'XPO:0102998', 'abnormal morula cell morphology', 0.40425531914893614, 5.43643956286526, 1.4824674062251753, 'HP:0025461', 'Abnormal cell morphology'),
(55318, 'HP:0012176', 'Abnormal natural killer cell morphology', 'XPO:0140600', 'abnormally necrotic apoptotic cell', 0.40425531914893614, 5.43643956286526, 1.4824674062251753, 'HP:0025461', 'Abnormal cell morphology'),
(55319, 'HP:0012176', 'Abnormal natural killer cell morphology', 'XPO:0102336', 'abnormal Merkel cell morphology', 0.4418604651162791, 5.43643956286526, 1.5498863551319448, 'HP:0025461', 'Abnormal cell morphology'),
(55320, 'HP:0012176', 'Abnormal natural killer cell morphology', 'XPO:0102608', 'abnormal multiciliated cell morphology', 0.4222222222222222, 5.43643956286526, 1.5150530001322648, 'HP:0025461', 'Abnormal cell morphology'),
(55321, 'HP:0012176', 'Abnormal natural killer cell morphology', 'XPO:0103112', 'abnormal stage V oocyte morphology', 0.40425531914893614, 5.43643956286526, 1.4824674062251753, 'HP:0025461', 'Abnormal cell morphology'),
(55322, 'HP:0012176', 'Abnormal natural killer cell morphology', 'XPO:0102061', 'abnormal spermatid morphology', 0.4222222222222222, 5.43643956286526, 1.5150530001322648, 'HP:0025461', 'Abnormal cell morphology'),
(55323, 'HP:0012176', 'Abnormal natural killer cell morphology', 'XPO:0103219', 'abnormal hemangioblast morphology', 0.44680851063829785, 5.574066539846944, 1.5781445969453445, 'UPHENO:0004459', 'abnormal hematopoietic system'),
(55324, 'HP:0012176', 'Abnormal natural killer cell morphology', 'XPO:0102929', 'abnormal barrier cell morphology', 0.4418604651162791, 5.43643956286526, 1.5498863551319448, 'HP:0025461', 'Abnormal cell morphology'),
(55325, 'HP:0012176', 'Abnormal natural killer cell morphology', 'XPO:0103100', 'abnormal stage I oocyte morphology', 0.40425531914893614, 5.43643956286526, 1.4824674062251753, 'HP:0025461', 'Abnormal cell morphology'),
(55326, 'HP:0012176', 'Abnormal natural killer cell morphology', 'XPO:0141154', 'abnormally necrotic barrier cell', 0.40425531914893614, 5.43643956286526, 1.4824674062251753, 'HP:0025461', 'Abnormal cell morphology'),
(55327, 'HP:0012176', 'Abnormal natural killer cell morphology', 'XPO:0140239', 'abnormally necrotic absorptive cell', 0.40425531914893614, 5.43643956286526, 1.4824674062251753, 'HP:0025461', 'Abnormal cell morphology'),
(55328, 'HP:0012176', 'Abnormal natural killer cell morphology', 'XPO:0140381', 'abnormally necrotic ciliated cell', 0.40425531914893614, 5.43643956286526, 1.4824674062251753, 'HP:0025461', 'Abnormal cell morphology'),
(55329, 'HP:0012176', 'Abnormal natural killer cell morphology', 'XPO:0125284', 'absent thymocyte', 0.4533333333333333, 8.504690711543915, 1.9635324772545122, 'UPHENO:0084888', 'abnormal lymphocyte morphology'),
(55330, 'HP:0012176', 'Abnormal natural killer cell morphology', 'XPO:0139929', 'abnormally necrotic barrier epithelial cell', 0.40425531914893614, 5.43643956286526, 1.4824674062251753, 'HP:0025461', 'Abnormal cell morphology'),
(55331, 'HP:0012176', 'Abnormal natural killer cell morphology', 'XPO:0140429', 'abnormally necrotic hemangioblast', 0.4117647058823529, 5.574066539846944, 1.5149930261716527, 'UPHENO:0004459', 'abnormal hematopoietic system'),
(55332, 'HP:0012176', 'Abnormal natural killer cell morphology', 'XPO:0103099', 'abnormal alkali secreting cell morphology', 0.4418604651162791, 5.43643956286526, 1.5498863551319448, 'HP:0025461', 'Abnormal cell morphology'),
(55333, 'HP:0012176', 'Abnormal natural killer cell morphology', 'XPO:0140471', 'abnormally necrotic multiciliated cell precursor', 0.40425531914893614, 5.43643956286526, 1.4824674062251753, 'HP:0025461', 'Abnormal cell morphology'),
(55334, 'HP:0012176', 'Abnormal natural killer cell morphology', 'XPO:0101850', 'abnormal epithelial cell morphology', 0.41304347826086957, 5.43643956286526, 1.4984945466703803, 'HP:0025461', 'Abnormal cell morphology'),
(55335, 'HP:0012176', 'Abnormal natural killer cell morphology', 'XPO:0102285', 'abnormal myoblast morphology', 0.4418604651162791, 5.43643956286526, 1.5498863551319448, 'HP:0025461', 'Abnormal cell morphology'),
(55336, 'HP:0012176', 'Abnormal natural killer cell morphology', 'XPO:0140068', 'abnormally necrotic myoblast', 0.40425531914893614, 5.43643956286526, 1.4824674062251753, 'HP:0025461', 'Abnormal cell morphology'),
(55337, 'HP:0012176', 'Abnormal natural killer cell morphology', 'XPO:0102739', 'abnormal erythroid cell morphology', 0.44680851063829785, 5.574066539846944, 1.5781445969453445, 'HP:0001871', 'Abnormality of blood and blood-forming tissues'),
(55338, 'HP:0012176', 'Abnormal natural killer cell morphology', 'XPO:0139950', 'abnormally necrotic B cell', 0.41509433962264153, 6.786309419308587, 1.6783797624145764, 'UPHENO:0087123', 'abnormal immune system morphology'),
(55339, 'HP:0012176', 'Abnormal natural killer cell morphology', 'XPO:0140899', 'abnormally necrotic mucus secreting cell', 0.40425531914893614, 5.43643956286526, 1.4824674062251753, 'HP:0025461', 'Abnormal cell morphology'),
(55340, 'HP:0012176', 'Abnormal natural killer cell morphology', 'XPO:0140752', 'abnormally necrotic melanoblast', 0.40425531914893614, 5.43643956286526, 1.4824674062251753, 'HP:0025461', 'Abnormal cell morphology'),
(55341, 'HP:0012176', 'Abnormal natural killer cell morphology', 'XPO:0101808', 'abnormal stage VI oocyte morphology', 0.40425531914893614, 5.43643956286526, 1.4824674062251753, 'HP:0025461', 'Abnormal cell morphology'),
(55342, 'HP:0012176', 'Abnormal natural killer cell morphology', 'XPO:0140331', 'abnormally necrotic myeloid cell', 0.4117647058823529, 5.574066539846944, 1.5149930261716527, 'HP:0001871', 'Abnormality of blood and blood-forming tissues'),
(55343, 'HP:0012176', 'Abnormal natural killer cell morphology', 'XPO:0101921', 'abnormal chondroblast morphology', 0.4418604651162791, 5.43643956286526, 1.5498863551319448, 'HP:0025461', 'Abnormal cell morphology'),
(55344, 'HP:0030290', 'Unossified sacrum', 'XPO:0126886', 'abnormally localised vertebral column', 0.4166666666666667, 8.05344015541032, 1.8318297040812228, 'UPHENO:0002813', 'abnormal vertebral column'),
(55345, 'HP:0030290', 'Unossified sacrum', 'XPO:0102216', 'abnormal vertebral column morphology', 0.4642857142857143, 8.361863005979023, 1.9703536582274415, 'UPHENO:0076695', 'abnormal vertebral column morphology'),
(55346, 'HP:0030290', 'Unossified sacrum', 'XPO:0128227', 'decreased size of the vertebral column', 0.40625, 8.361863005979023, 1.843097079965941, 'UPHENO:0076695', 'abnormal vertebral column morphology'),
(55347, 'HP:0030290', 'Unossified sacrum', 'XPO:0100693', 'abnormal vertebral centrum', 0.43103448275862066, 8.05344015541032, 1.863145300778979, 'UPHENO:0002813', 'abnormal vertebral column'),
(55348, 'HP:0030290', 'Unossified sacrum', 'XPO:0100226', 'abnormal vertebral element', 0.43859649122807015, 8.05344015541032, 1.8794176210938882, 'UPHENO:0002813', 'abnormal vertebral column'),
(55349, 'HP:0030290', 'Unossified sacrum', 'XPO:0102461', 'abnormal postcranial axial skeleton morphology', 0.41818181818181815, 6.272837960958401, 1.6196255072310737, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(55350, 'HP:0030290', 'Unossified sacrum', 'XPO:0101858', 'abnormal vertebral element morphology', 0.40625, 8.361863005979023, 1.843097079965941, 'UPHENO:0076695', 'abnormal vertebral column morphology'),
(55351, 'HP:0030290', 'Unossified sacrum', 'XPO:0129707', 'increased size of the vertebral column', 0.40625, 8.361863005979023, 1.843097079965941, 'UPHENO:0076695', 'abnormal vertebral column morphology'),
(55352, 'HP:0030290', 'Unossified sacrum', 'XPO:0140103', 'abnormally necrotic vertebral column', 0.41935483870967744, 8.361863005979023, 1.8725885058348382, 'UPHENO:0076695', 'abnormal vertebral column morphology'),
(55353, 'HP:0030290', 'Unossified sacrum', 'XPO:0100584', 'abnormal vertebral column', 0.49019607843137253, 8.05344015541032, 1.9868982817607654, 'UPHENO:0002813', 'abnormal vertebral column'),
(55354, 'HP:0030290', 'Unossified sacrum', 'XPO:0102217', 'abnormal elastica externa morphology', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(55355, 'HP:0030290', 'Unossified sacrum', 'XPO:0102097', 'abnormal skeletal system morphology', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(55356, 'HP:0033131', 'Renal medullary hyperechogenicity', 'XPO:0100778', 'abnormal mesonephric kidney', 0.4418604651162791, 6.880013295263146, 1.7435612620872136, 'HP:0000077', 'Abnormality of the kidney'),
(55357, 'HP:0033131', 'Renal medullary hyperechogenicity', 'XPO:0102393', 'abnormal ureter morphology', 0.41304347826086957, 7.340144605965611, 1.7412061506282923, 'UPHENO:0087427', 'abnormal renal system morphology'),
(55358, 'HP:0033131', 'Renal medullary hyperechogenicity', 'XPO:0100565', 'abnormal pronephric kidney', 0.40425531914893614, 6.880013295263146, 1.6677175931270638, 'HP:0000077', 'Abnormality of the kidney'),
(55359, 'HP:0033131', 'Renal medullary hyperechogenicity', 'XPO:0100147', 'abnormal mesonephric mesenchyme', 0.5277777777777778, 6.880013295263146, 1.9055492982485522, 'HP:0000077', 'Abnormality of the kidney'),
(55360, 'HP:0033131', 'Renal medullary hyperechogenicity', 'XPO:0126710', 'abnormally localised kidney', 0.46, 7.603795021646889, 1.870226111986882, 'HP:0012210', 'Abnormal renal morphology'),
(55361, 'HP:0033131', 'Renal medullary hyperechogenicity', 'XPO:0100761', 'abnormal ureter', 0.4594594594594595, 6.828345551150745, 1.7712560390677927, 'HP:0010935', 'Abnormality of the upper urinary tract'),
(55362, 'HP:0033131', 'Renal medullary hyperechogenicity', 'XPO:0140552', 'abnormally necrotic kidney', 0.42592592592592593, 7.603795021646889, 1.7996259153351557, 'HP:0012210', 'Abnormal renal morphology'),
(55363, 'HP:0033131', 'Renal medullary hyperechogenicity', 'XPO:0107300', 'abnormal embryonic kidney', 0.5, 6.880013295263146, 1.8547254911796445, 'HP:0000077', 'Abnormality of the kidney'),
(55364, 'HP:0033131', 'Renal medullary hyperechogenicity', 'XPO:0126656', 'abnormally localised embryonic kidney', 0.4423076923076923, 7.603795021646889, 1.833907584586899, 'HP:0012210', 'Abnormal renal morphology'),
(55365, 'HP:0033131', 'Renal medullary hyperechogenicity', 'XPO:0103182', 'abnormal pronephric sinus morphology', 0.42592592592592593, 7.603795021646889, 1.7996259153351557, 'HP:0012210', 'Abnormal renal morphology'),
(55366, 'HP:0033131', 'Renal medullary hyperechogenicity', 'XPO:0102198', 'abnormal kidney morphology', 0.5, 7.603795021646889, 1.9498455094759288, 'HP:0012210', 'Abnormal renal morphology'),
(55367, 'HP:0033131', 'Renal medullary hyperechogenicity', 'XPO:0126885', 'abnormally localised adult kidney', 0.4423076923076923, 7.603795021646889, 1.833907584586899, 'HP:0012210', 'Abnormal renal morphology'),
(55368, 'HP:0033131', 'Renal medullary hyperechogenicity', 'XPO:0101701', 'abnormal urinary system morphology', 0.4358974358974359, 7.340144605965611, 1.788728658253343, 'UPHENO:0087427', 'abnormal renal system morphology'),
(55369, 'HP:0033131', 'Renal medullary hyperechogenicity', 'XPO:0101717', 'abnormal mesonephric sinus morphology', 0.5897435897435898, 7.603795021646889, 2.1176140752602852, 'HP:0012210', 'Abnormal renal morphology'),
(55370, 'HP:0033131', 'Renal medullary hyperechogenicity', 'XPO:0100567', 'abnormal mesonephric collecting duct', 0.45098039215686275, 7.603795021646889, 1.8517997895946297, 'HP:0012210', 'Abnormal renal morphology'),
(55371, 'HP:0033131', 'Renal medullary hyperechogenicity', 'XPO:0128342', 'decreased size of the mesonephric mesenchyme', 0.41818181818181815, 7.603795021646889, 1.7831906312097294, 'HP:0012210', 'Abnormal renal morphology'),
(55372, 'HP:0033131', 'Renal medullary hyperechogenicity', 'XPO:0107388', 'abnormal adult kidney morphology', 0.4791666666666667, 7.603795021646889, 1.9087915324988045, 'HP:0012210', 'Abnormal renal morphology'),
(55373, 'HP:0033131', 'Renal medullary hyperechogenicity', 'XPO:0107301', 'abnormal adult kidney', 0.5, 6.880013295263146, 1.8547254911796445, 'HP:0000077', 'Abnormality of the kidney'),
(55374, 'HP:0033131', 'Renal medullary hyperechogenicity', 'XPO:0101277', 'abnormal glomerulus', 0.4222222222222222, 6.880013295263146, 1.7043751061443133, 'HP:0000077', 'Abnormality of the kidney'),
(55375, 'HP:0033131', 'Renal medullary hyperechogenicity', 'XPO:0141613', 'metaplastic kidney', 0.4634146341463415, 6.880013295263146, 1.7855808142300187, 'HP:0000077', 'Abnormality of the kidney'),
(55376, 'HP:0033131', 'Renal medullary hyperechogenicity', 'XPO:0129822', 'increased size of the mesonephric mesenchyme', 0.41818181818181815, 7.603795021646889, 1.7831906312097294, 'HP:0012210', 'Abnormal renal morphology'),
(55377, 'HP:0033131', 'Renal medullary hyperechogenicity', 'XPO:0101779', 'abnormal mesonephric mesenchyme morphology', 0.48936170212765956, 7.603795021646889, 1.9289909472112474, 'HP:0012210', 'Abnormal renal morphology'),
(55378, 'HP:0033131', 'Renal medullary hyperechogenicity', 'XPO:0100069', 'abnormal urinary system', 0.46875, 6.355235291121788, 1.725982775902859, 'HP:0000079', 'Abnormality of the urinary system'),
(55379, 'HP:0033131', 'Renal medullary hyperechogenicity', 'XPO:0140354', 'abnormally necrotic adult kidney', 0.40350877192982454, 7.603795021646889, 1.7516272409365097, 'HP:0012210', 'Abnormal renal morphology'),
(55380, 'HP:0033131', 'Renal medullary hyperechogenicity', 'XPO:0130678', 'increased size of the mesonephric sinus', 0.5227272727272727, 7.603795021646889, 1.9936677341128566, 'HP:0012210', 'Abnormal renal morphology'),
(55381, 'HP:0033131', 'Renal medullary hyperechogenicity', 'XPO:0125259', 'absent adult kidney', 0.40350877192982454, 7.603795021646889, 1.7516272409365097, 'HP:0012210', 'Abnormal renal morphology'),
(55382, 'HP:0033131', 'Renal medullary hyperechogenicity', 'XPO:0139936', 'abnormally necrotic embryonic kidney', 0.40350877192982454, 7.603795021646889, 1.7516272409365097, 'HP:0012210', 'Abnormal renal morphology'),
(55383, 'HP:0033131', 'Renal medullary hyperechogenicity', 'XPO:0100271', 'abnormal mesonephric nephron', 0.4318181818181818, 6.880013295263146, 1.7236341932224046, 'HP:0000077', 'Abnormality of the kidney'),
(55384, 'HP:0033131', 'Renal medullary hyperechogenicity', 'XPO:0125038', 'absent embryonic kidney', 0.40350877192982454, 7.603795021646889, 1.7516272409365097, 'HP:0012210', 'Abnormal renal morphology'),
(55385, 'HP:0033131', 'Renal medullary hyperechogenicity', 'XPO:0107387', 'abnormal embryonic kidney morphology', 0.4791666666666667, 7.603795021646889, 1.9087915324988045, 'HP:0012210', 'Abnormal renal morphology'),
(55386, 'HP:0033131', 'Renal medullary hyperechogenicity', 'XPO:0129202', 'decreased size of the mesonephric sinus', 0.5227272727272727, 7.603795021646889, 1.9936677341128566, 'HP:0012210', 'Abnormal renal morphology'),
(55387, 'HP:0033131', 'Renal medullary hyperechogenicity', 'XPO:0141643', 'neoplastic kidney', 0.46938775510204084, 7.603795021646889, 1.8892136659115366, 'HP:0012210', 'Abnormal renal morphology'),
(55388, 'HP:0033131', 'Renal medullary hyperechogenicity', 'XPO:0127733', 'abnormally localised mesonephric sinus', 0.475, 6.880013295263146, 1.8077627928602786, 'HP:0000077', 'Abnormality of the kidney'),
(55389, 'HP:0033131', 'Renal medullary hyperechogenicity', 'XPO:0100085', 'abnormal mesonephric sinus', 0.5757575757575758, 6.880013295263146, 1.9902813308827976, 'HP:0000077', 'Abnormality of the kidney'),
(55390, 'HP:0033131', 'Renal medullary hyperechogenicity', 'XPO:0100501', 'abnormal urogenital system', 0.41935483870967744, 5.4478002382576385, 1.5114765596055648, 'HP:0000119', 'Abnormality of the genitourinary system'),
(55391, 'HP:0033131', 'Renal medullary hyperechogenicity', 'XPO:0126072', 'absent mesonephric sinus', 0.4318181818181818, 6.880013295263146, 1.7236341932224046, 'HP:0000077', 'Abnormality of the kidney'),
(55392, 'HP:0033131', 'Renal medullary hyperechogenicity', 'XPO:0127342', 'abnormally localised mesonephric mesenchyme', 0.40425531914893614, 6.880013295263146, 1.6677175931270638, 'HP:0000077', 'Abnormality of the kidney'),
(55393, 'HP:0033131', 'Renal medullary hyperechogenicity', 'XPO:0140815', 'abnormally necrotic mesonephric mesenchyme', 0.4339622641509434, 7.603795021646889, 1.816524181984252, 'HP:0012210', 'Abnormal renal morphology'),
(55394, 'HP:0033131', 'Renal medullary hyperechogenicity', 'XPO:0101903', 'abnormal mesonephric nephron morphology', 0.41818181818181815, 7.603795021646889, 1.7831906312097294, 'HP:0012210', 'Abnormal renal morphology'),
(55395, 'HP:0033131', 'Renal medullary hyperechogenicity', 'XPO:0125089', 'absent kidney', 0.41818181818181815, 7.603795021646889, 1.7831906312097294, 'HP:0012210', 'Abnormal renal morphology'),
(55396, 'HP:0033131', 'Renal medullary hyperechogenicity', 'XPO:0128275', 'decreased size of the kidney', 0.40350877192982454, 7.603795021646889, 1.7516272409365097, 'HP:0012210', 'Abnormal renal morphology'),
(55397, 'HP:0033131', 'Renal medullary hyperechogenicity', 'XPO:0100566', 'abnormal kidney', 0.5135135135135135, 6.880013295263146, 1.8796222493549772, 'HP:0000077', 'Abnormality of the kidney'),
(55398, 'HP:0033131', 'Renal medullary hyperechogenicity', 'XPO:0100270', 'abnormal mesonephric tubule', 0.40425531914893614, 6.880013295263146, 1.6677175931270638, 'HP:0000077', 'Abnormality of the kidney'),
(55399, 'HP:0033131', 'Renal medullary hyperechogenicity', 'XPO:0102410', 'abnormal mesonephric kidney morphology', 0.41818181818181815, 7.603795021646889, 1.7831906312097294, 'HP:0012210', 'Abnormal renal morphology'),
(55400, 'HP:0001457', 'Abnormality of the musculature of the upper arm', 'XPO:0100751', 'abnormal coracoid bone', 0.4098360655737705, 9.992881323162637, 2.023720130163899, 'HP:0001446', 'Abnormality of the musculature of the upper limbs'),
(55401, 'HP:0001457', 'Abnormality of the musculature of the upper arm', 'XPO:0102400', 'abnormal pectoral girdle morphology', 0.423728813559322, 9.992881323162637, 2.057734615324049, 'HP:0001446', 'Abnormality of the musculature of the upper limbs'),
(55402, 'HP:0001457', 'Abnormality of the musculature of the upper arm', 'XPO:0125790', 'absent pectoral girdle', 0.44642857142857145, 9.992881323162637, 2.112133455431912, 'HP:0001446', 'Abnormality of the musculature of the upper limbs'),
(55403, 'HP:0001457', 'Abnormality of the musculature of the upper arm', 'XPO:0100768', 'abnormal pectoral girdle', 0.5681818181818182, 9.992881323162637, 2.3828078980626364, 'HP:0001446', 'Abnormality of the musculature of the upper limbs'),
(55404, 'HP:0001457', 'Abnormality of the musculature of the upper arm', 'XPO:0101233', 'abnormal scapula', 0.4098360655737705, 9.992881323162637, 2.023720130163899, 'HP:0001446', 'Abnormality of the musculature of the upper limbs'),
(55405, 'HP:0001457', 'Abnormality of the musculature of the upper arm', 'XPO:0127441', 'abnormally localised pectoral girdle', 0.46296296296296297, 9.992881323162637, 2.150891430525639, 'HP:0001446', 'Abnormality of the musculature of the upper limbs'),
(55406, 'HP:0011206', 'EEG with generalized slow activity grade 1', 'XPO:0100273', 'abnormal visual system', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(55407, 'HP:0011206', 'EEG with generalized slow activity grade 1', 'XPO:0100274', 'abnormal sensory system', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(55408, 'HP:0011206', 'EEG with generalized slow activity grade 1', 'XPO:0100031', 'abnormal central nervous system', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(55409, 'HP:0011206', 'EEG with generalized slow activity grade 1', 'XPO:0100032', 'abnormal nervous system', 0.43333333333333335, 3.94131651835137, 1.3068679445984308, 'UPHENO:0004523', 'abnormal nervous system'),
(55410, 'HP:0011206', 'EEG with generalized slow activity grade 1', 'XPO:0100642', 'abnormal gustatory system', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(55411, 'HP:0011206', 'EEG with generalized slow activity grade 1', 'XPO:0100587', 'abnormal vestibuloauditory system', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(55412, 'HP:0011206', 'EEG with generalized slow activity grade 1', 'XPO:0100427', 'abnormal olfactory system', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(55413, 'HP:0011206', 'EEG with generalized slow activity grade 1', 'XPO:0107253', 'abnormal enteric nervous system', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(55414, 'HP:0011055', 'Agenesis of permanent molar', 'XPO:0128989', 'decreased size of the tooth', 0.4326923076923077, 9.872199840740173, 2.0667909742132844, 'HP:0006482', 'Abnormal dental morphology'),
(55415, 'HP:0011055', 'Agenesis of permanent molar', 'XPO:0130466', 'increased size of the tooth', 0.4326923076923077, 9.872199840740173, 2.0667909742132844, 'HP:0006482', 'Abnormal dental morphology'),
(55416, 'HP:0011055', 'Agenesis of permanent molar', 'XPO:0126089', 'absent tongue', 0.40229885057471265, 7.884497199543557, 1.7809896576723612, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(55417, 'HP:0011055', 'Agenesis of permanent molar', 'XPO:0126046', 'absent tooth', 0.46078431372549017, 11.802658907487096, 2.332054906047987, 'UPHENO:0063844', 'abnormally decreased number of calcareous tooth'),
(55418, 'HP:0011055', 'Agenesis of permanent molar', 'XPO:0102890', 'abnormal dentine morphology', 0.4368932038834951, 9.872199840740173, 2.0767997057489933, 'HP:0006482', 'Abnormal dental morphology'),
(55419, 'HP:0011055', 'Agenesis of permanent molar', 'XPO:0141006', 'abnormally necrotic cementum', 0.41284403669724773, 9.872199840740173, 2.0188310561642098, 'HP:0006482', 'Abnormal dental morphology'),
(55420, 'HP:0011055', 'Agenesis of permanent molar', 'XPO:0101567', 'abnormal tongue', 0.4155844155844156, 7.884497199543557, 1.8101586010207147, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(55421, 'HP:0011055', 'Agenesis of permanent molar', 'XPO:0101659', 'abnormal lower jaw morphology', 0.40860215053763443, 7.312692920701687, 1.7285780438325729, 'UPHENO:0076800', 'abnormal mouth morphology'),
(55422, 'HP:0011055', 'Agenesis of permanent molar', 'XPO:0101816', 'abnormal tooth morphology', 0.4891304347826087, 9.872199840740173, 2.197451569514569, 'HP:0006482', 'Abnormal dental morphology'),
(55423, 'HP:0011055', 'Agenesis of permanent molar', 'XPO:0139736', 'abnormally necrotic tooth', 0.45, 9.872199840740173, 2.1077215016061963, 'HP:0006482', 'Abnormal dental morphology'),
(55424, 'HP:0011055', 'Agenesis of permanent molar', 'XPO:0103096', 'abnormal oral cavity morphology', 0.42168674698795183, 7.884497199543557, 1.8234001139933984, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(55425, 'HP:0011055', 'Agenesis of permanent molar', 'XPO:0102861', 'abnormal cementum morphology', 0.44554455445544555, 9.872199840740173, 2.097261280703408, 'HP:0006482', 'Abnormal dental morphology'),
(55426, 'HP:0011055', 'Agenesis of permanent molar', 'XPO:0103199', 'abnormal tongue morphology', 0.42168674698795183, 7.884497199543557, 1.8234001139933984, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(55427, 'HP:0011055', 'Agenesis of permanent molar', 'XPO:0129990', 'increased size of the cementum', 0.40540540540540543, 9.872199840740173, 2.0005607160689847, 'HP:0006482', 'Abnormal dental morphology'),
(55428, 'HP:0011055', 'Agenesis of permanent molar', 'XPO:0140890', 'abnormally necrotic dentine', 0.4017857142857143, 9.872199840740173, 1.9916096165120074, 'HP:0006482', 'Abnormal dental morphology'),
(55429, 'HP:0011055', 'Agenesis of permanent molar', 'XPO:0128510', 'decreased size of the cementum', 0.40540540540540543, 9.872199840740173, 2.0005607160689847, 'HP:0006482', 'Abnormal dental morphology'),
(55430, 'HP:0100827', 'Lymphocytosis', 'XPO:0131163', 'abnormally increased number of neutrophil', 0.4153846153846154, 10.497804325958676, 2.0882112949415097, 'UPHENO:0085938', 'abnormally increased number of anatomical entity in the blood'),
(55431, 'HP:0100827', 'Lymphocytosis', 'XPO:0130966', 'abnormally increased number of thrombocyte', 0.4032258064516129, 10.497804325958676, 2.057422080008358, 'UPHENO:0085938', 'abnormally increased number of anatomical entity in the blood'),
(55432, 'HP:0100827', 'Lymphocytosis', 'XPO:0131138', 'abnormally increased number of macrophage', 0.4153846153846154, 10.497804325958676, 2.0882112949415097, 'UPHENO:0085938', 'abnormally increased number of anatomical entity in the blood'),
(55433, 'HP:0100827', 'Lymphocytosis', 'XPO:0131005', 'abnormally increased number of thymocyte', 0.5783132530120482, 11.189682030596343, 2.5438438268267634, 'HP:0100827', 'Lymphocytosis'),
(55434, 'HP:0025370', 'Abnormal ossification of the sacrum', 'XPO:0101446', 'abnormal transverse process', 0.4032258064516129, 8.05344015541032, 1.8020418700394085, 'UPHENO:0002813', 'abnormal vertebral column'),
(55435, 'HP:0025370', 'Abnormal ossification of the sacrum', 'XPO:0140350', 'abnormally necrotic notochordal sheath', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(55436, 'HP:0025370', 'Abnormal ossification of the sacrum', 'XPO:0102216', 'abnormal vertebral column morphology', 0.5416666666666666, 8.361863005979023, 2.1282251905218983, 'UPHENO:0076695', 'abnormal vertebral column morphology'),
(55437, 'HP:0025370', 'Abnormal ossification of the sacrum', 'XPO:0128227', 'decreased size of the vertebral column', 0.4642857142857143, 8.361863005979023, 1.9703536582274415, 'UPHENO:0076695', 'abnormal vertebral column morphology'),
(55438, 'HP:0025370', 'Abnormal ossification of the sacrum', 'XPO:0100927', 'abnormal sacral vertebra', 0.4098360655737705, 8.05344015541032, 1.816752660002781, 'UPHENO:0002813', 'abnormal vertebral column'),
(55439, 'HP:0025370', 'Abnormal ossification of the sacrum', 'XPO:0129832', 'increased size of the skeletal system', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(55440, 'HP:0025370', 'Abnormal ossification of the sacrum', 'XPO:0102605', 'abnormal dermal skeleton morphology', 0.43478260869565216, 4.638757693672553, 1.4201588541997616, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(55441, 'HP:0025370', 'Abnormal ossification of the sacrum', 'XPO:0102097', 'abnormal skeletal system morphology', 0.4878048780487805, 4.638757693672553, 1.5042634845863214, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(55442, 'HP:0025370', 'Abnormal ossification of the sacrum', 'XPO:0128580', 'decreased size of the postcranial axial skeleton', 0.41818181818181815, 6.272837960958401, 1.6196255072310737, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(55443, 'HP:0025370', 'Abnormal ossification of the sacrum', 'XPO:0102054', 'abnormal notochord morphology', 0.46511627906976744, 4.638757693672553, 1.4688640910537754, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(55444, 'HP:0025370', 'Abnormal ossification of the sacrum', 'XPO:0102325', 'abnormal vertebral centrum morphology', 0.45614035087719296, 8.361863005979023, 1.9529933757015898, 'UPHENO:0076695', 'abnormal vertebral column morphology'),
(55445, 'HP:0025370', 'Abnormal ossification of the sacrum', 'XPO:0102980', 'abnormal perichordal tissue morphology', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(55446, 'HP:0025370', 'Abnormal ossification of the sacrum', 'XPO:0101858', 'abnormal vertebral element morphology', 0.4642857142857143, 8.361863005979023, 1.9703536582274415, 'UPHENO:0076695', 'abnormal vertebral column morphology'),
(55447, 'HP:0025370', 'Abnormal ossification of the sacrum', 'XPO:0101957', 'abnormal axial skeleton morphology', 0.45652173913043476, 6.211345574613551, 1.6839282300806968, 'UPHENO:0087089', 'abnormal axial skeleton plus cranial skeleton morphology'),
(55448, 'HP:0025370', 'Abnormal ossification of the sacrum', 'XPO:0102728', 'abnormal tendon morphology', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(55449, 'HP:0025370', 'Abnormal ossification of the sacrum', 'XPO:0139774', 'abnormally necrotic elastica externa', 0.43478260869565216, 4.638757693672553, 1.4201588541997616, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(55450, 'HP:0025370', 'Abnormal ossification of the sacrum', 'XPO:0100253', 'abnormal vertebra', 0.4166666666666667, 8.05344015541032, 1.8318297040812228, 'UPHENO:0002813', 'abnormal vertebral column'),
(55451, 'HP:0025370', 'Abnormal ossification of the sacrum', 'XPO:0126886', 'abnormally localised vertebral column', 0.4807692307692308, 8.05344015541032, 1.9677007466997247, 'UPHENO:0002813', 'abnormal vertebral column'),
(55452, 'HP:0025370', 'Abnormal ossification of the sacrum', 'XPO:0102093', 'abnormal craniofacial skeleton morphology', 0.42857142857142855, 6.211345574613551, 1.6315652749010534, 'UPHENO:0087089', 'abnormal axial skeleton plus cranial skeleton morphology'),
(55453, 'HP:0025370', 'Abnormal ossification of the sacrum', 'XPO:0102806', 'abnormal articular system morphology', 0.47619047619047616, 4.638757693672553, 1.4862477031377266, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(55454, 'HP:0025370', 'Abnormal ossification of the sacrum', 'XPO:0140683', 'abnormally necrotic flexural organ', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(55455, 'HP:0025370', 'Abnormal ossification of the sacrum', 'XPO:0128890', 'decreased size of the elastica externa', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(55456, 'HP:0025370', 'Abnormal ossification of the sacrum', 'XPO:0101860', 'abnormal skeletal subdivision morphology', 0.45454545454545453, 4.638757693672553, 1.452076521536181, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(55457, 'HP:0025370', 'Abnormal ossification of the sacrum', 'XPO:0102542', 'abnormal vacuolated notochordal tissue morphology', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(55458, 'HP:0025370', 'Abnormal ossification of the sacrum', 'XPO:0140510', 'abnormally necrotic postcranial axial skeleton', 0.4339622641509434, 6.272837960958401, 1.6499015013598524, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(55459, 'HP:0025370', 'Abnormal ossification of the sacrum', 'XPO:0102828', 'abnormal occipital region morphology', 0.40350877192982454, 6.272837960958401, 1.5909573036826314, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(55460, 'HP:0025370', 'Abnormal ossification of the sacrum', 'XPO:0102272', 'abnormal notochordal sheath morphology', 0.46511627906976744, 4.638757693672553, 1.4688640910537754, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(55461, 'HP:0025370', 'Abnormal ossification of the sacrum', 'XPO:0141703', 'abnormally necrotic posterior notochord', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(55462, 'HP:0025370', 'Abnormal ossification of the sacrum', 'XPO:0102217', 'abnormal elastica externa morphology', 0.4878048780487805, 4.638757693672553, 1.5042634845863214, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(55463, 'HP:0025370', 'Abnormal ossification of the sacrum', 'XPO:0141719', 'abnormal anterior notochord morphology', 0.46511627906976744, 4.638757693672553, 1.4688640910537754, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(55464, 'HP:0025370', 'Abnormal ossification of the sacrum', 'XPO:0125260', 'absent vertebral column', 0.45454545454545453, 8.05344015541032, 1.913283725978873, 'UPHENO:0002813', 'abnormal vertebral column'),
(55465, 'HP:0025370', 'Abnormal ossification of the sacrum', 'XPO:0129786', 'increased size of the articular system', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(55466, 'HP:0025370', 'Abnormal ossification of the sacrum', 'XPO:0140432', 'abnormally necrotic skeleton', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(55467, 'HP:0025370', 'Abnormal ossification of the sacrum', 'XPO:0141723', 'abnormal posterior notochord morphology', 0.46511627906976744, 4.638757693672553, 1.4688640910537754, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(55468, 'HP:0025370', 'Abnormal ossification of the sacrum', 'XPO:0103218', 'abnormal joint morphology', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(55469, 'HP:0025370', 'Abnormal ossification of the sacrum', 'XPO:0139917', 'abnormally necrotic notochord', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(55470, 'HP:0025370', 'Abnormal ossification of the sacrum', 'XPO:0130060', 'increased size of the postcranial axial skeleton', 0.41818181818181815, 6.272837960958401, 1.6196255072310737, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(55471, 'HP:0025370', 'Abnormal ossification of the sacrum', 'XPO:0141699', 'abnormally necrotic anterior notochord', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(55472, 'HP:0025370', 'Abnormal ossification of the sacrum', 'XPO:0102514', 'abnormal perichondrial cell morphology', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(55473, 'HP:0025370', 'Abnormal ossification of the sacrum', 'XPO:0100693', 'abnormal vertebral centrum', 0.5, 8.05344015541032, 2.0066689008665977, 'UPHENO:0002813', 'abnormal vertebral column'),
(55474, 'HP:0025370', 'Abnormal ossification of the sacrum', 'XPO:0140559', 'abnormally necrotic articular system', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(55475, 'HP:0025370', 'Abnormal ossification of the sacrum', 'XPO:0139795', 'abnormally necrotic vertebral element', 0.40625, 8.361863005979023, 1.843097079965941, 'UPHENO:0076695', 'abnormal vertebral column morphology'),
(55476, 'HP:0025370', 'Abnormal ossification of the sacrum', 'XPO:0102164', 'abnormal mandibular mesenchyme morphology', 0.40384615384615385, 6.211345574613551, 1.5838017617482976, 'UPHENO:0087089', 'abnormal axial skeleton plus cranial skeleton morphology'),
(55477, 'HP:0025370', 'Abnormal ossification of the sacrum', 'XPO:0101070', 'abnormal rib', 0.4032258064516129, 8.05344015541032, 1.8020418700394085, 'UPHENO:0002813', 'abnormal vertebral column'),
(55478, 'HP:0025370', 'Abnormal ossification of the sacrum', 'XPO:0102567', 'abnormal skeleton morphology', 0.46511627906976744, 4.638757693672553, 1.4688640910537754, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(55479, 'HP:0025370', 'Abnormal ossification of the sacrum', 'XPO:0100895', 'abnormal presacral vertebra', 0.4098360655737705, 8.05344015541032, 1.816752660002781, 'UPHENO:0002813', 'abnormal vertebral column'),
(55480, 'HP:0025370', 'Abnormal ossification of the sacrum', 'XPO:0100226', 'abnormal vertebral element', 0.5102040816326531, 8.05344015541032, 2.0270416962841815, 'UPHENO:0002813', 'abnormal vertebral column'),
(55481, 'HP:0025370', 'Abnormal ossification of the sacrum', 'XPO:0139998', 'abnormally necrotic axial skeleton', 0.40384615384615385, 6.211345574613551, 1.5838017617482976, 'UPHENO:0087089', 'abnormal axial skeleton plus cranial skeleton morphology'),
(55482, 'HP:0025370', 'Abnormal ossification of the sacrum', 'XPO:0128306', 'decreased size of the articular system', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(55483, 'HP:0025370', 'Abnormal ossification of the sacrum', 'XPO:0140019', 'abnormally necrotic skeletal system', 0.43478260869565216, 4.638757693672553, 1.4201588541997616, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(55484, 'HP:0025370', 'Abnormal ossification of the sacrum', 'XPO:0139771', 'abnormally necrotic skeletal subdivision', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(55485, 'HP:0025370', 'Abnormal ossification of the sacrum', 'XPO:0140103', 'abnormally necrotic vertebral column', 0.48148148148148145, 8.361863005979023, 2.006509952146755, 'UPHENO:0076695', 'abnormal vertebral column morphology'),
(55486, 'HP:0025370', 'Abnormal ossification of the sacrum', 'XPO:0128352', 'decreased size of the skeletal system', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(55487, 'HP:0025370', 'Abnormal ossification of the sacrum', 'XPO:0107372', 'abnormal flexural organ morphology', 0.46511627906976744, 4.638757693672553, 1.4688640910537754, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(55488, 'HP:0025370', 'Abnormal ossification of the sacrum', 'XPO:0102144', 'abnormal cranial skeleton morphology', 0.44680851063829785, 6.211345574613551, 1.665917784661915, 'UPHENO:0087089', 'abnormal axial skeleton plus cranial skeleton morphology'),
(55489, 'HP:0025370', 'Abnormal ossification of the sacrum', 'XPO:0101982', 'abnormal appendicular skeleton morphology', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(55490, 'HP:0025370', 'Abnormal ossification of the sacrum', 'XPO:0102010', 'abnormal perichondrium morphology', 0.45454545454545453, 4.638757693672553, 1.452076521536181, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(55491, 'HP:0025370', 'Abnormal ossification of the sacrum', 'XPO:0101226', 'abnormal postsacral vertebra', 0.4098360655737705, 8.05344015541032, 1.816752660002781, 'UPHENO:0002813', 'abnormal vertebral column'),
(55492, 'HP:0025370', 'Abnormal ossification of the sacrum', 'XPO:0129707', 'increased size of the vertebral column', 0.4642857142857143, 8.361863005979023, 1.9703536582274415, 'UPHENO:0076695', 'abnormal vertebral column morphology'),
(55493, 'HP:0025370', 'Abnormal ossification of the sacrum', 'XPO:0102461', 'abnormal postcranial axial skeleton morphology', 0.48936170212765956, 6.272837960958401, 1.7520521287180928, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(55494, 'HP:0025370', 'Abnormal ossification of the sacrum', 'XPO:0130368', 'increased size of the elastica externa', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(55495, 'HP:0025370', 'Abnormal ossification of the sacrum', 'XPO:0127548', 'abnormally localised vertebral element', 0.4166666666666667, 8.05344015541032, 1.8318297040812228, 'UPHENO:0002813', 'abnormal vertebral column'),
(55496, 'HP:0025370', 'Abnormal ossification of the sacrum', 'XPO:0100584', 'abnormal vertebral column', 0.5813953488372093, 8.05344015541032, 2.163846724815409, 'UPHENO:0002813', 'abnormal vertebral column'),
(55497, 'HP:0025370', 'Abnormal ossification of the sacrum', 'XPO:0102130', 'abnormal endoskeleton morphology', 0.43478260869565216, 4.638757693672553, 1.4201588541997616, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(55498, 'HP:0025370', 'Abnormal ossification of the sacrum', 'XPO:0126787', 'abnormally localised vertebral centrum', 0.4098360655737705, 8.05344015541032, 1.816752660002781, 'UPHENO:0002813', 'abnormal vertebral column'),
(55499, 'HP:0032208', 'Increased urinary type 1 collagen N-terminal telopeptide level', 'XPO:0100069', 'abnormal urinary system', 0.46875, 6.355235291121788, 1.725982775902859, 'HP:0000079', 'Abnormality of the urinary system'),
(55500, 'HP:0032208', 'Increased urinary type 1 collagen N-terminal telopeptide level', 'XPO:0100501', 'abnormal urogenital system', 0.41935483870967744, 5.4478002382576385, 1.5114765596055648, 'HP:0000119', 'Abnormality of the genitourinary system'),
(55501, 'HP:0032208', 'Increased urinary type 1 collagen N-terminal telopeptide level', 'XPO:0100085', 'abnormal mesonephric sinus', 0.40540540540540543, 6.355235291121788, 1.6051313776896794, 'HP:0000079', 'Abnormality of the urinary system'),
(55502, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0141718', 'abnormal posterior notochord', 0.42857142857142855, 3.9037819259951223, 1.293464107292913, 'HP:0033127', 'Abnormality of the musculoskeletal system'),
(55503, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0101220', 'abnormal centriole', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(55504, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0139779', 'abnormally necrotic muscle', 0.425, 6.895202660022325, 1.7118589692230748, 'HP:0011805', 'Abnormal skeletal muscle morphology'),
(55505, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0100429', 'abnormal spermatid', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(55506, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0100081', 'abnormal anatomical entity in vitro', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(55507, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0100802', 'abnormal exocrine cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(55508, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0141315', 'abnormal anatomical region', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(55509, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0100378', 'abnormal perichondrium', 0.41379310344827586, 3.9037819259951223, 1.270967363209146, 'HP:0033127', 'Abnormality of the musculoskeletal system'),
(55510, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0102228', 'abnormal myocyte morphology', 0.425, 6.895202660022325, 1.7118589692230748, 'HP:0011805', 'Abnormal skeletal muscle morphology'),
(55511, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0100274', 'abnormal sensory system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(55512, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0100417', 'abnormal dense regular connective tissue', 0.4444444444444444, 3.9037819259951223, 1.3171993734173904, 'HP:0033127', 'Abnormality of the musculoskeletal system'),
(55513, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0101513', 'abnormal basal body', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(55514, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0115505', 'dead whole organism', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(55515, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0107260', 'abnormal anterior-posterior axis', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(55516, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0100545', 'abnormal male organism', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(55517, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0101569', 'abnormal activin-induced ectoderm', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(55518, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0101373', 'abnormal oxygen accumulating cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(55519, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0115512', 'abnormally semi-erect whole organism', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(55520, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0131675', 'abnormal spindle microtubule', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(55521, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0107284', 'abnormal migrating myoblast', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(55522, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0100721', 'abnormal centromere', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(55523, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0100176', 'abnormal stage VI oocyte', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(55524, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0100258', 'abnormal organ part', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(55525, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0101141', 'abnormal Keller explant', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(55526, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0100202', 'abnormal embryo', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(55527, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0101547', 'abnormal lampbrush chromosome', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(55528, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0101366', 'abnormal morula cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(55529, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0100644', 'abnormal smooth muscle myocyte', 0.4117647058823529, 5.968280811662945, 1.5676502776568768, 'UPHENO:0002816', 'abnormal musculature'),
(55530, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0100477', 'abnormal pericyte', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(55531, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0101498', 'abnormal stage II oocyte', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(55532, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0100031', 'abnormal central nervous system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(55533, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0101535', 'abnormal absorptive cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(55534, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0142057', 'abnormal desmosome', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(55535, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0100377', 'abnormal connective tissue', 0.46153846153846156, 3.9037819259951223, 1.3422911399191462, 'HP:0033127', 'Abnormality of the musculoskeletal system'),
(55536, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0100501', 'abnormal urogenital system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(55537, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0100481', 'abnormal anatomical line', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(55538, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0101237', 'abnormal mucus secreting cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(55539, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0100688', 'abnormal adipose tissue', 0.4444444444444444, 3.9037819259951223, 1.3171993734173904, 'HP:0033127', 'Abnormality of the musculoskeletal system'),
(55540, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0101448', 'abnormal myelin accumulating cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(55541, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0100025', 'abnormal oocyte', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(55542, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0131667', 'abnormal actin cytoskeleton', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(55543, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0101240', 'abnormal ciliated non-epidermal cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(55544, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0100653', 'abnormal myoblast', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(55545, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0101907', 'abnormal skeletal muscle morphology', 0.4594594594594595, 6.895202660022325, 1.7799062017525769, 'HP:0011805', 'Abnormal skeletal muscle morphology'),
(55546, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0100307', 'abnormal blastomere', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(55547, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0103736', 'increased size of the muscle', 0.40476190476190477, 6.895202660022325, 1.6706032929423995, 'HP:0011805', 'Abnormal skeletal muscle morphology'),
(55548, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0101435', 'abnormal paracrine cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(55549, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0100317', 'abnormal respiratory system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(55550, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0100852', 'abnormal interdigital region', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(55551, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0100894', 'abnormal nucleus', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(55552, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0100465', 'abnormal skeletal system', 0.4444444444444444, 3.9037819259951223, 1.3171993734173904, 'HP:0033127', 'Abnormality of the musculoskeletal system'),
(55553, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0107285', 'abnormal flexural organ', 0.42857142857142855, 3.9037819259951223, 1.293464107292913, 'HP:0033127', 'Abnormality of the musculoskeletal system'),
(55554, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0103098', 'abnormal secondary myofiber morphology', 0.425, 6.895202660022325, 1.7118589692230748, 'HP:0011805', 'Abnormal skeletal muscle morphology'),
(55555, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0100839', 'abnormal skeletal myocyte', 0.4117647058823529, 5.968280811662945, 1.5676502776568768, 'UPHENO:0002816', 'abnormal musculature'),
(55556, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0100596', 'abnormal myocyte', 0.4375, 5.968280811662945, 1.6158969197020392, 'UPHENO:0002816', 'abnormal musculature'),
(55557, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0101466', 'abnormal secondary myofiber', 0.4375, 5.968280811662945, 1.6158969197020392, 'UPHENO:0002816', 'abnormal musculature'),
(55558, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0100392', 'abnormal cilium', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(55559, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0100715', 'abnormal ciliated cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(55560, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0115508', 'abnormally peramorphic growth of whole organism', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(55561, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0100585', 'abnormal elastica externa', 0.46153846153846156, 3.9037819259951223, 1.3422911399191462, 'HP:0033127', 'Abnormality of the musculoskeletal system'),
(55562, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0100581', 'abnormal immune system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(55563, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0100638', 'abnormal polar body', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(55564, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0101409', 'abnormal perivitelline space', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(55565, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0141776', 'abnormal metabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(55566, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0101174', 'abnormal articular system', 0.42857142857142855, 3.9037819259951223, 1.293464107292913, 'HP:0033127', 'Abnormality of the musculoskeletal system'),
(55567, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0101713', 'abnormal anatomical entity in vitro morphology', 0.4166666666666667, 2.485033483301678, 1.0175611126818702, 'UPHENO:0076692', 'abnormal anatomical entity morphology'),
(55568, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0101228', 'abnormal mesenchymal stem cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(55569, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0100956', 'abnormal centrosome', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(55570, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0141714', 'abnormal anterior notochord', 0.42857142857142855, 3.9037819259951223, 1.293464107292913, 'HP:0033127', 'Abnormality of the musculoskeletal system'),
(55571, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0100791', 'abnormal multiciliated cell precursor', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(55572, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0100691', 'abnormal keratin accumulating cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(55573, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0100344', 'abnormal portion of organism substance', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(55574, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0101004', 'abnormal acid secreting cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(55575, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0100032', 'abnormal nervous system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(55576, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0100275', 'abnormal skeletal muscle', 0.4827586206896552, 5.968280811662945, 1.6974212831607063, 'UPHENO:0002816', 'abnormal musculature'),
(55577, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0101326', 'abnormal cementoblast', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(55578, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0101061', 'abnormal plasma membrane', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(55579, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0100010', 'abnormal multicellular anatomical structure', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(55580, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0101221', 'abnormal larval immune system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(55581, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0100100', 'abnormal muscle', 0.5, 5.968280811662945, 1.7274664702481124, 'UPHENO:0002816', 'abnormal musculature'),
(55582, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0100386', 'abnormal limb', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(55583, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0100533', 'abnormal melanoblast', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(55584, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0101472', 'abnormal zygote cortex', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(55585, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0107270', 'abnormal proximal-distal axis', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(55586, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0101732', 'abnormal muscle morphology', 0.4857142857142857, 6.895202660022325, 1.8300542163739266, 'HP:0011805', 'Abnormal skeletal muscle morphology'),
(55587, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0107253', 'abnormal enteric nervous system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(55588, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0141307', 'abnormal M band morphology', 0.40476190476190477, 6.895202660022325, 1.6706032929423995, 'HP:0011805', 'Abnormal skeletal muscle morphology'),
(55589, 'HP:0030236', 'Abnormality of muscle size', 'XPO:00000000', 'Xenopus phenotype', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(55590, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0100754', 'abnormal electrically active cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(55591, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0100728', 'abnormal cell condensation', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(55592, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0100976', 'abnormal multiciliated cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(55593, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0141284', 'abnormal myofibril morphology', 0.425, 6.895202660022325, 1.7118589692230748, 'HP:0011805', 'Abnormal skeletal muscle morphology'),
(55594, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0131685', 'abnormal cortical actin cytoskeleton', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(55595, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0101109', 'abnormal egg cell-free extract', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(55596, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0100289', 'abnormal chondroblast', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(55597, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0100546', 'abnormal whole organism', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(55598, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0100172', 'abnormal stem cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(55599, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0102378', 'abnormal smooth muscle morphology', 0.4473684210526316, 6.895202660022325, 1.7563302442456807, 'HP:0011805', 'Abnormal skeletal muscle morphology'),
(55600, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0101096', 'abnormal tendon', 0.42857142857142855, 3.9037819259951223, 1.293464107292913, 'HP:0033127', 'Abnormality of the musculoskeletal system'),
(55601, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0100626', 'abnormal primordial germ cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(55602, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0131677', 'abnormal actin filament', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(55603, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0100026', 'abnormal germ cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(55604, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0100969', 'abnormal disaggregated/reaggregated ectoderm treated with activin', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(55605, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0141499', 'abnormal tadpole', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(55606, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0101241', 'abnormal nucleate erythrocyte', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(55607, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0100422', 'abnormal notochord', 0.4444444444444444, 3.9037819259951223, 1.3171993734173904, 'HP:0033127', 'Abnormality of the musculoskeletal system'),
(55608, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0100004', 'abnormal cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(55609, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0101153', 'abnormal musculature of face', 0.40476190476190477, 6.895202660022325, 1.6706032929423995, 'HP:0011805', 'Abnormal skeletal muscle morphology'),
(55610, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0100640', 'abnormal notochordal sheath', 0.42857142857142855, 3.9037819259951223, 1.293464107292913, 'HP:0033127', 'Abnormality of the musculoskeletal system'),
(55611, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0101297', 'abnormal barrier cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(55612, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0100062', 'abnormal anatomical space', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(55613, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0131666', 'abnormal adherens junction', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(55614, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0100935', 'abnormal skeleton', 0.41379310344827586, 3.9037819259951223, 1.270967363209146, 'HP:0033127', 'Abnormality of the musculoskeletal system'),
(55615, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0101071', 'abnormal endoplasmic reticulum', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(55616, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0131655', 'abnormal myofibril', 0.4117647058823529, 5.968280811662945, 1.5676502776568768, 'UPHENO:0002816', 'abnormal musculature'),
(55617, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0100888', 'abnormal microtubule', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(55618, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0107259', 'abnormal animal-vegetal axis', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(55619, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0100573', 'abnormal extraembryonic structure', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(55620, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0102113', 'abnormal anatomical line morphology', 0.4166666666666667, 2.485033483301678, 1.0175611126818702, 'UPHENO:0076692', 'abnormal anatomical entity morphology'),
(55621, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0107258', 'abnormal anatomical axis', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(55622, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0100724', 'abnormal kinetochore', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(55623, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0101481', 'abnormal skeletal muscle satellite cell', 0.42424242424242425, 5.968280811662945, 1.591225288920281, 'UPHENO:0002816', 'abnormal musculature'),
(55624, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0101461', 'abnormal sperm entry point', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(55625, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0103353', 'decreased size of the muscle', 0.40476190476190477, 6.895202660022325, 1.6706032929423995, 'HP:0011805', 'Abnormal skeletal muscle morphology'),
(55626, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0101467', 'abnormal alkali secreting cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(55627, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0100902', 'abnormal spermatocyte', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(55628, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0100308', 'abnormal early embryonic cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(55629, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0101132', 'abnormal apoptotic cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(55630, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0100746', 'abnormal smooth muscle', 0.4827586206896552, 5.968280811662945, 1.6974212831607063, 'UPHENO:0002816', 'abnormal musculature'),
(55631, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0100225', 'abnormal endocrine system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(55632, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0107262', 'abnormal left-right axis', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(55633, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0101157', 'abnormal female organism', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(55634, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0100006', 'abnormal anatomical structure', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(55635, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0100239', 'abnormal acellular anatomical structure', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(55636, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0101976', 'abnormal portion of organism substance morphology', 0.4166666666666667, 2.485033483301678, 1.0175611126818702, 'UPHENO:0076692', 'abnormal anatomical entity morphology'),
(55637, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0100768', 'abnormal pectoral girdle', 0.40476190476190477, 6.895202660022325, 1.6706032929423995, 'HP:0011805', 'Abnormal skeletal muscle morphology'),
(55638, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0107261', 'abnormal dorsal-ventral axis', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(55639, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0100416', 'abnormal ligament', 0.42857142857142855, 3.9037819259951223, 1.293464107292913, 'HP:0033127', 'Abnormality of the musculoskeletal system'),
(55640, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0100285', 'abnormal progenitor cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(55641, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0100549', 'abnormal mitotic cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(55642, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0103113', 'abnormal skeletal muscle satellite cell morphology', 0.4146341463414634, 6.895202660022325, 1.6908537691916898, 'HP:0011805', 'Abnormal skeletal muscle morphology'),
(55643, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0100899', 'abnormal secondary spermatogonium', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(55644, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0101480', 'abnormal stage V oocyte', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(55645, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0100704', 'abnormal Merkel cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(55646, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0101468', 'abnormal stage I oocyte', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(55647, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0107312', 'abnormal filopodium', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(55648, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0100108', 'abnormal cell part', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(55649, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0100515', 'abnormal somatic stem cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(55650, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0101264', 'abnormal mitotic spindle', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(55651, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0100084', 'abnormal anatomical group', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(55652, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0101638', 'abnormal anatomical structure morphology', 0.4166666666666667, 2.485033483301678, 1.0175611126818702, 'UPHENO:0076692', 'abnormal anatomical entity morphology'),
(55653, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0100674', 'abnormal secondary oogonium', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(55654, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0141294', 'abnormal sarcomere morphology', 0.4146341463414634, 6.895202660022325, 1.6908537691916898, 'HP:0011805', 'Abnormal skeletal muscle morphology'),
(55655, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0115509', 'abnormally semi-viable whole organism', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(55656, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0100574', 'abnormal gastrula cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(55657, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0100337', 'abnormal zygote', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(55658, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0101113', 'abnormal stage IV oocyte', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(55659, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0100599', 'abnormal adult immune system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(55660, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0101333', 'abnormal barrier epithelial cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(55661, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0100232', 'abnormal lymphatic system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(55662, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0100372', 'abnormal hematological system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(55663, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0100907', 'abnormal cytoplasm', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(55664, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0101110', 'abnormal cell-free extract', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(55665, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0100917', 'abnormal stage III oocyte', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(55666, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0100437', 'abnormal proepicardium', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(55667, 'HP:0030236', 'Abnormality of muscle size', 'XPO:0100423', 'abnormal process', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(55668, 'HP:0034165', 'Reduced circulating interleukin 21 concentration', 'XPO:0100232', 'abnormal lymphatic system', 0.4482758620689655, 5.64885357140806, 1.5913028324062968, 'HP:0002715', 'Abnormality of the immune system'),
(55669, 'HP:0034165', 'Reduced circulating interleukin 21 concentration', 'XPO:0101451', 'abnormal dorsal lymph space', 0.41935483870967744, 5.64885357140806, 1.5391147060347428, 'HP:0002715', 'Abnormality of the immune system'),
(55670, 'HP:0034165', 'Reduced circulating interleukin 21 concentration', 'XPO:0100599', 'abnormal adult immune system', 0.43333333333333335, 5.64885357140806, 1.5645563421015427, 'HP:0002715', 'Abnormality of the immune system'),
(55671, 'HP:0034165', 'Reduced circulating interleukin 21 concentration', 'XPO:0100581', 'abnormal immune system', 0.4482758620689655, 5.64885357140806, 1.5913028324062968, 'HP:0002715', 'Abnormality of the immune system'),
(55672, 'HP:0034165', 'Reduced circulating interleukin 21 concentration', 'XPO:0100745', 'abnormal anterior lymph sac', 0.40625, 5.64885357140806, 1.5148751642906173, 'HP:0002715', 'Abnormality of the immune system'),
(55673, 'HP:0034165', 'Reduced circulating interleukin 21 concentration', 'XPO:0101221', 'abnormal larval immune system', 0.43333333333333335, 5.64885357140806, 1.5645563421015427, 'HP:0002715', 'Abnormality of the immune system'),
(55674, 'HP:0008056', 'Aplasia/Hypoplasia affecting the eye', 'XPO:0101483', 'abnormal nostril', 0.48, 5.788671267106304, 1.6669019791850466, 'UPHENO:0087472', 'abnormal face morphology'),
(55675, 'HP:0008056', 'Aplasia/Hypoplasia affecting the eye', 'XPO:0133371', 'eye fused with olfactory pit', 0.47692307692307695, 6.887869297006056, 1.8124524320853552, 'HP:0012372', 'Abnormal eye morphology'),
(55676, 'HP:0008056', 'Aplasia/Hypoplasia affecting the eye', 'XPO:0128564', 'decreased size of the hyaloid blood vessel', 0.41333333333333333, 6.887869297006056, 1.6873013886368484, 'HP:0012372', 'Abnormal eye morphology'),
(55677, 'HP:0008056', 'Aplasia/Hypoplasia affecting the eye', 'XPO:0102003', 'abnormal hyaloid blood vessel morphology', 0.4626865671641791, 6.887869297006056, 1.7851959556606887, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(55678, 'HP:0008056', 'Aplasia/Hypoplasia affecting the eye', 'XPO:0140820', 'abnormally necrotic globe', 0.4090909090909091, 6.575878401988876, 1.640162209521029, 'UPHENO:0087924', 'abnormal camera-type eye morphology'),
(55679, 'HP:0008056', 'Aplasia/Hypoplasia affecting the eye', 'XPO:0133370', 'olfactory pit fused with brain', 0.41379310344827586, 5.788671267106304, 1.5476796336638217, 'UPHENO:0087472', 'abnormal face morphology'),
(55680, 'HP:0008056', 'Aplasia/Hypoplasia affecting the eye', 'XPO:0102212', 'abnormal globe morphology', 0.4426229508196721, 6.575878401988876, 1.7060582353834428, 'UPHENO:0087924', 'abnormal camera-type eye morphology'),
(55681, 'HP:0008056', 'Aplasia/Hypoplasia affecting the eye', 'XPO:0115417', 'abnormally wholly ventralized eye', 0.4492753623188406, 6.887869297006056, 1.759133301946505, 'HP:0012372', 'Abnormal eye morphology'),
(55682, 'HP:0008056', 'Aplasia/Hypoplasia affecting the eye', 'XPO:0103048', 'abnormal cornea morphology', 0.44285714285714284, 6.887869297006056, 1.7465228647932265, 'HP:0012372', 'Abnormal eye morphology'),
(55683, 'HP:0008056', 'Aplasia/Hypoplasia affecting the eye', 'XPO:0127783', 'abnormally localised hyaloid vascular plexus', 0.45588235294117646, 6.887869297006056, 1.7720208976957377, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(55684, 'HP:0008056', 'Aplasia/Hypoplasia affecting the eye', 'XPO:0141839', 'edematous pharyngeal region', 0.4666666666666667, 4.5318002188002176, 1.4542489821577214, 'UPHENO:0087907', 'abnormal head morphology'),
(55685, 'HP:0008056', 'Aplasia/Hypoplasia affecting the eye', 'XPO:0130413', 'increased size of the central retina', 0.4189189189189189, 6.887869297006056, 1.6986638159319787, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(55686, 'HP:0008056', 'Aplasia/Hypoplasia affecting the eye', 'XPO:0141337', 'increased pigmentation in the eye', 0.47692307692307695, 6.887869297006056, 1.8124524320853552, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(55687, 'HP:0008056', 'Aplasia/Hypoplasia affecting the eye', 'XPO:0133372', 'eye fused with olfactory epithelium', 0.47692307692307695, 6.887869297006056, 1.8124524320853552, 'HP:0012372', 'Abnormal eye morphology'),
(55688, 'HP:0008056', 'Aplasia/Hypoplasia affecting the eye', 'XPO:0103160', 'abnormal choroid morphology', 0.42857142857142855, 6.575878401988876, 1.6787595422967447, 'UPHENO:0087924', 'abnormal camera-type eye morphology'),
(55689, 'HP:0008056', 'Aplasia/Hypoplasia affecting the eye', 'XPO:0130863', 'increased size of the sclera', 0.44285714285714284, 6.887869297006056, 1.7465228647932265, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(55690, 'HP:0008056', 'Aplasia/Hypoplasia affecting the eye', 'XPO:0128935', 'decreased size of the central retina', 0.4189189189189189, 6.887869297006056, 1.6986638159319787, 'HP:0012372', 'Abnormal eye morphology'),
(55691, 'HP:0008056', 'Aplasia/Hypoplasia affecting the eye', 'XPO:0140914', 'abnormally necrotic intercanthal region', 0.42857142857142855, 4.5318002188002176, 1.3936283915633758, 'UPHENO:0087907', 'abnormal head morphology'),
(55692, 'HP:0008056', 'Aplasia/Hypoplasia affecting the eye', 'XPO:0102259', 'abnormal pharyngeal region morphology', 0.4883720930232558, 4.5318002188002176, 1.4876843610183952, 'UPHENO:0087907', 'abnormal head morphology'),
(55693, 'HP:0008056', 'Aplasia/Hypoplasia affecting the eye', 'XPO:0130062', 'increased size of the head region', 0.4117647058823529, 4.5318002188002176, 1.3660290568695288, 'UPHENO:0087907', 'abnormal head morphology'),
(55694, 'HP:0008056', 'Aplasia/Hypoplasia affecting the eye', 'XPO:0125990', 'absent hyaloid vein', 0.44285714285714284, 6.887869297006056, 1.7465228647932265, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(55695, 'HP:0008056', 'Aplasia/Hypoplasia affecting the eye', 'XPO:0100710', 'abnormal hyaloid vein', 0.5535714285714286, 6.887869297006056, 1.9526719249676645, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(55696, 'HP:0008056', 'Aplasia/Hypoplasia affecting the eye', 'XPO:0103115', 'abnormal nostril morphology', 0.41379310344827586, 5.788671267106304, 1.5476796336638217, 'UPHENO:0087472', 'abnormal face morphology'),
(55697, 'HP:0008056', 'Aplasia/Hypoplasia affecting the eye', 'XPO:0130122', 'increased size of the retinal layer', 0.4189189189189189, 6.887869297006056, 1.6986638159319787, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(55698, 'HP:0008056', 'Aplasia/Hypoplasia affecting the eye', 'XPO:0102082', 'abnormal circumpharyngeal ridge morphology', 0.4375, 4.5318002188002176, 1.4080705222839853, 'UPHENO:0087907', 'abnormal head morphology'),
(55699, 'HP:0008056', 'Aplasia/Hypoplasia affecting the eye', 'XPO:0140335', 'abnormally necrotic pharyngeal region', 0.45652173913043476, 4.5318002188002176, 1.4383550734357495, 'UPHENO:0087907', 'abnormal head morphology'),
(55700, 'HP:0008056', 'Aplasia/Hypoplasia affecting the eye', 'XPO:0103358', 'decreased size of the pharyngeal region', 0.4375, 4.5318002188002176, 1.4080705222839853, 'UPHENO:0087907', 'abnormal head morphology'),
(55701, 'HP:0008056', 'Aplasia/Hypoplasia affecting the eye', 'XPO:0101359', 'abnormal hyaloid artery', 0.44285714285714284, 6.887869297006056, 1.7465228647932265, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(55702, 'HP:0008056', 'Aplasia/Hypoplasia affecting the eye', 'XPO:0127907', 'abnormally localised optic choroid vascular plexus', 0.4696969696969697, 6.887869297006056, 1.7986693238259617, 'HP:0012372', 'Abnormal eye morphology'),
(55703, 'HP:0008056', 'Aplasia/Hypoplasia affecting the eye', 'XPO:0100779', 'abnormal optic choroid vascular plexus', 0.5636363636363636, 6.887869297006056, 1.9703435243040868, 'HP:0012372', 'Abnormal eye morphology'),
(55704, 'HP:0008056', 'Aplasia/Hypoplasia affecting the eye', 'XPO:0102196', 'abnormal central retina morphology', 0.4492753623188406, 6.887869297006056, 1.759133301946505, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(55705, 'HP:0008056', 'Aplasia/Hypoplasia affecting the eye', 'XPO:0103336', 'decreased size of the eye', 0.4246575342465753, 6.887869297006056, 1.7102589253909142, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(55706, 'HP:0008056', 'Aplasia/Hypoplasia affecting the eye', 'XPO:0103186', 'abnormal peripheral retina morphology', 0.4305555555555556, 6.887869297006056, 1.7220947685207388, 'HP:0012372', 'Abnormal eye morphology'),
(55707, 'HP:0008056', 'Aplasia/Hypoplasia affecting the eye', 'XPO:0126243', 'absent optic choroid vascular plexus', 0.43661971830985913, 6.887869297006056, 1.734179792355427, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(55708, 'HP:0008056', 'Aplasia/Hypoplasia affecting the eye', 'XPO:0102784', 'abnormal retinal progenitor cell region morphology', 0.4246575342465753, 6.887869297006056, 1.7102589253909142, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(55709, 'HP:0008056', 'Aplasia/Hypoplasia affecting the eye', 'XPO:0140553', 'abnormally necrotic retinal stem cell region', 0.40789473684210525, 6.887869297006056, 1.6761639640277146, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(55710, 'HP:0008056', 'Aplasia/Hypoplasia affecting the eye', 'XPO:0140017', 'abnormally necrotic lateral nasal prominence', 0.4117647058823529, 4.5318002188002176, 1.3660290568695288, 'UPHENO:0087907', 'abnormal head morphology'),
(55711, 'HP:0008056', 'Aplasia/Hypoplasia affecting the eye', 'XPO:0103739', 'increased size of the pharyngeal region', 0.4375, 4.5318002188002176, 1.4080705222839853, 'UPHENO:0087907', 'abnormal head morphology'),
(55712, 'HP:0008056', 'Aplasia/Hypoplasia affecting the eye', 'XPO:0140863', 'abnormally necrotic circumpharyngeal ridge', 0.40384615384615385, 4.5318002188002176, 1.3528303989641963, 'UPHENO:0087907', 'abnormal head morphology'),
(55713, 'HP:0008056', 'Aplasia/Hypoplasia affecting the eye', 'XPO:0141339', 'decreased pigmentation in the head', 0.44680851063829785, 4.5318002188002176, 1.422971154406314, 'UPHENO:0087907', 'abnormal head morphology'),
(55714, 'HP:0008056', 'Aplasia/Hypoplasia affecting the eye', 'XPO:0126871', 'abnormally localised choana', 0.4067796610169492, 5.788671267106304, 1.5345076525622334, 'UPHENO:0087472', 'abnormal face morphology'),
(55715, 'HP:0008056', 'Aplasia/Hypoplasia affecting the eye', 'XPO:0140192', 'abnormally necrotic retina', 0.4189189189189189, 6.887869297006056, 1.6986638159319787, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(55716, 'HP:0008056', 'Aplasia/Hypoplasia affecting the eye', 'XPO:0125589', 'absent hyaloid blood vessel', 0.4696969696969697, 6.887869297006056, 1.7986693238259617, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(55717, 'HP:0008056', 'Aplasia/Hypoplasia affecting the eye', 'XPO:0115423', 'abnormally incomplete structure of eye', 0.49206349206349204, 6.887869297006056, 1.8409967461029664, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(55718, 'HP:0008056', 'Aplasia/Hypoplasia affecting the eye', 'XPO:0130893', 'increased size of the pupil', 0.4025974025974026, 6.887869297006056, 1.6652442128423794, 'HP:0012372', 'Abnormal eye morphology'),
(55719, 'HP:0008056', 'Aplasia/Hypoplasia affecting the eye', 'XPO:0133354', 'fused eyes', 0.47692307692307695, 6.887869297006056, 1.8124524320853552, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(55720, 'HP:0008056', 'Aplasia/Hypoplasia affecting the eye', 'XPO:0102756', 'abnormal Muller cell morphology', 0.4025974025974026, 6.887869297006056, 1.6652442128423794, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(55721, 'HP:0008056', 'Aplasia/Hypoplasia affecting the eye', 'XPO:0100329', 'abnormal retinal blood vessel', 0.45588235294117646, 6.887869297006056, 1.7720208976957377, 'HP:0012372', 'Abnormal eye morphology'),
(55722, 'HP:0008056', 'Aplasia/Hypoplasia affecting the eye', 'XPO:0101823', 'abnormal lens epithelium morphology', 0.41333333333333333, 6.887869297006056, 1.6873013886368484, 'HP:0012372', 'Abnormal eye morphology'),
(55723, 'HP:0008056', 'Aplasia/Hypoplasia affecting the eye', 'XPO:0102947', 'abnormal hyaloid vascular plexus morphology', 0.4189189189189189, 6.887869297006056, 1.6986638159319787, 'HP:0012372', 'Abnormal eye morphology'),
(55724, 'HP:0008056', 'Aplasia/Hypoplasia affecting the eye', 'XPO:0102572', 'abnormal hatching gland primordium morphology', 0.42857142857142855, 4.5318002188002176, 1.3936283915633758, 'UPHENO:0087907', 'abnormal head morphology'),
(55725, 'HP:0008056', 'Aplasia/Hypoplasia affecting the eye', 'XPO:0142059', 'abnormal nasal region morphology', 0.4666666666666667, 4.5318002188002176, 1.4542489821577214, 'UPHENO:0087907', 'abnormal head morphology'),
(55726, 'HP:0008056', 'Aplasia/Hypoplasia affecting the eye', 'XPO:0129780', 'increased size of the retina', 0.40789473684210525, 6.887869297006056, 1.6761639640277146, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(55727, 'HP:0008056', 'Aplasia/Hypoplasia affecting the eye', 'XPO:0102805', 'abnormal retinal layer morphology', 0.4626865671641791, 6.887869297006056, 1.7851959556606887, 'HP:0012372', 'Abnormal eye morphology'),
(55728, 'HP:0008056', 'Aplasia/Hypoplasia affecting the eye', 'XPO:0140538', 'abnormally necrotic optic disc', 0.43548387096774194, 6.575878401988876, 1.692243771302257, 'UPHENO:0087924', 'abnormal camera-type eye morphology'),
(55729, 'HP:0008056', 'Aplasia/Hypoplasia affecting the eye', 'XPO:0141298', 'abnormal intercanthal region morphology', 0.45652173913043476, 4.5318002188002176, 1.4383550734357495, 'UPHENO:0087907', 'abnormal head morphology'),
(55730, 'HP:0008056', 'Aplasia/Hypoplasia affecting the eye', 'XPO:0102538', 'abnormal lateral nasal prominence morphology', 0.44680851063829785, 4.5318002188002176, 1.422971154406314, 'UPHENO:0087907', 'abnormal head morphology'),
(55731, 'HP:0008056', 'Aplasia/Hypoplasia affecting the eye', 'XPO:0102342', 'abnormal hyaloid vein morphology', 0.41333333333333333, 6.887869297006056, 1.6873013886368484, 'HP:0012372', 'Abnormal eye morphology'),
(55732, 'HP:0008056', 'Aplasia/Hypoplasia affecting the eye', 'XPO:0103210', 'abnormal pupil morphology', 0.4305555555555556, 6.887869297006056, 1.7220947685207388, 'HP:0012372', 'Abnormal eye morphology'),
(55733, 'HP:0008056', 'Aplasia/Hypoplasia affecting the eye', 'XPO:0141343', 'decreased pigmentation in the eye', 0.47692307692307695, 6.887869297006056, 1.8124524320853552, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(55734, 'HP:0008056', 'Aplasia/Hypoplasia affecting the eye', 'XPO:0101634', 'abnormal head morphology', 0.4772727272727273, 4.5318002188002176, 1.4706816956370683, 'UPHENO:0087907', 'abnormal head morphology'),
(55735, 'HP:0008056', 'Aplasia/Hypoplasia affecting the eye', 'XPO:0102117', 'abnormal retina morphology', 0.4492753623188406, 6.887869297006056, 1.759133301946505, 'HP:0012372', 'Abnormal eye morphology'),
(55736, 'HP:0008056', 'Aplasia/Hypoplasia affecting the eye', 'XPO:0130048', 'increased size of the optic disc', 0.421875, 6.575878401988876, 1.6655925974976766, 'UPHENO:0087924', 'abnormal camera-type eye morphology'),
(55737, 'HP:0008056', 'Aplasia/Hypoplasia affecting the eye', 'XPO:0102804', 'abnormal pharyngeal pouch morphology', 0.44680851063829785, 4.5318002188002176, 1.422971154406314, 'UPHENO:0087907', 'abnormal head morphology'),
(55738, 'HP:0008056', 'Aplasia/Hypoplasia affecting the eye', 'XPO:0139731', 'abnormally necrotic eye', 0.4492753623188406, 6.887869297006056, 1.759133301946505, 'HP:0012372', 'Abnormal eye morphology'),
(55739, 'HP:0008056', 'Aplasia/Hypoplasia affecting the eye', 'XPO:0102476', 'abnormal lens transitional zone morphology', 0.45588235294117646, 6.887869297006056, 1.7720208976957377, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
