(464850, 'HP:0031925', 'Rosette', 'XPO:0129263', 'decreased size of the mitochondrial cloud', 0.43243243243243246, 3.6715585125471644, 1.2600400701560144, 'UPHENO:0086172', 'abnormal cell'),
(464851, 'HP:0031925', 'Rosette', 'XPO:0101666', 'abnormal blastomere V1.1 morphology', 0.43902439024390244, 5.43643956286526, 1.5449043867452603, 'HP:0025461', 'Abnormal cell morphology'),
(464852, 'HP:0031925', 'Rosette', 'XPO:0102704', 'abnormal mitochondrial cloud morphology', 0.5161290322580645, 3.6715585125471644, 1.376589242279565, 'UPHENO:0086172', 'abnormal cell'),
(464853, 'HP:0031925', 'Rosette', 'XPO:0141166', 'abnormally necrotic stage III oocyte', 0.47368421052631576, 5.43643956286526, 1.6047291305419304, 'HP:0025461', 'Abnormal cell morphology'),
(464854, 'HP:0031925', 'Rosette', 'XPO:0101514', 'abnormal dendrite', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(464855, 'HP:0031925', 'Rosette', 'XPO:0131004', 'abnormally increased number of proepicardium', 0.4117647058823529, 3.6715585125471644, 1.229560169755361, 'UPHENO:0086172', 'abnormal cell'),
(464856, 'HP:0031925', 'Rosette', 'XPO:0102533', 'abnormal blastomere D1.2.2 morphology', 0.43902439024390244, 5.43643956286526, 1.5449043867452603, 'HP:0025461', 'Abnormal cell morphology'),
(464857, 'HP:0031925', 'Rosette', 'XPO:0129486', 'increased size of the cell', 0.4864864864864865, 5.43643956286526, 1.626270082715184, 'HP:0025461', 'Abnormal cell morphology'),
(464858, 'HP:0031925', 'Rosette', 'XPO:0101239', 'abnormal olfactory epithelial support cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(464859, 'HP:0031925', 'Rosette', 'XPO:0102873', 'abnormal nucleate erythrocyte morphology', 0.6428571428571429, 5.43643956286526, 1.869452862390249, 'HP:0025461', 'Abnormal cell morphology'),
(464860, 'HP:0031925', 'Rosette', 'XPO:0107371', 'abnormal migrating myoblast morphology', 0.6, 5.43643956286526, 1.8060630492092893, 'HP:0025461', 'Abnormal cell morphology'),
(464861, 'HP:0031925', 'Rosette', 'XPO:0103150', 'abnormal B cell morphology', 0.5, 5.43643956286526, 1.6487024538808177, 'HP:0025461', 'Abnormal cell morphology'),
(464862, 'HP:0031925', 'Rosette', 'XPO:0130979', 'abnormally increased number of Merkel cell', 0.42424242424242425, 3.6715585125471644, 1.2480508339450433, 'UPHENO:0086172', 'abnormal cell'),
(464863, 'HP:0031925', 'Rosette', 'XPO:0102621', 'abnormal right blastomere morphology', 0.5294117647058824, 5.43643956286526, 1.696500828969256, 'HP:0025461', 'Abnormal cell morphology'),
(464864, 'HP:0031925', 'Rosette', 'XPO:0102998', 'abnormal morula cell morphology', 0.5625, 5.43643956286526, 1.748713027947041, 'HP:0025461', 'Abnormal cell morphology'),
(464865, 'HP:0031925', 'Rosette', 'XPO:0101061', 'abnormal plasma membrane', 0.52, 3.6715585125471644, 1.3817418089225373, 'UPHENO:0086172', 'abnormal cell'),
(464866, 'HP:0031925', 'Rosette', 'XPO:0140331', 'abnormally necrotic myeloid cell', 0.47368421052631576, 5.43643956286526, 1.6047291305419304, 'HP:0025461', 'Abnormal cell morphology'),
(464867, 'HP:0031925', 'Rosette', 'XPO:0127821', 'abnormally localised apoptotic cell', 0.45161290322580644, 3.6715585125471644, 1.2876813267322194, 'UPHENO:0086172', 'abnormal cell'),
(464868, 'HP:0031925', 'Rosette', 'XPO:0100859', 'abnormal blastomere V1.1.2', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(464869, 'HP:0031925', 'Rosette', 'XPO:0130352', 'increased size of the ciliary axoneme', 0.43243243243243246, 3.6715585125471644, 1.2600400701560144, 'UPHENO:0086172', 'abnormal cell'),
(464870, 'HP:0031925', 'Rosette', 'XPO:0130027', 'increased size of the zygote cortex', 0.4444444444444444, 3.6715585125471644, 1.2774207542365574, 'UPHENO:0086172', 'abnormal cell'),
(464871, 'HP:0031925', 'Rosette', 'XPO:0102133', 'abnormal urogenital system morphology', 0.4375, 2.7446671847279203, 1.0958065035937983, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(464872, 'HP:0031925', 'Rosette', 'XPO:0127168', 'abnormally localised chondroblast', 0.45161290322580644, 3.6715585125471644, 1.2876813267322194, 'UPHENO:0086172', 'abnormal cell'),
(464873, 'HP:0031925', 'Rosette', 'XPO:0101220', 'abnormal centriole', 0.5, 3.6715585125471644, 1.3549093166236559, 'UPHENO:0086172', 'abnormal cell'),
(464874, 'HP:0031925', 'Rosette', 'XPO:0100203', 'abnormal endocrine cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(464875, 'HP:0031925', 'Rosette', 'XPO:0128594', 'decreased size of the ciliated cell', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(464876, 'HP:0031925', 'Rosette', 'XPO:0102915', 'abnormal left-ventral blastomere morphology', 0.5294117647058824, 5.43643956286526, 1.696500828969256, 'HP:0025461', 'Abnormal cell morphology'),
(464877, 'HP:0031925', 'Rosette', 'XPO:0103082', 'abnormal myeloid cell morphology', 0.5294117647058824, 5.43643956286526, 1.696500828969256, 'HP:0025461', 'Abnormal cell morphology'),
(464878, 'HP:0031925', 'Rosette', 'XPO:0100332', 'abnormal germinal granule', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(464879, 'HP:0031925', 'Rosette', 'XPO:0101575', 'abnormal vitelline membrane', 0.48148148148148145, 3.6715585125471644, 1.3295816755533123, 'UPHENO:0086172', 'abnormal cell'),
(464880, 'HP:0031925', 'Rosette', 'XPO:0126314', 'absent absorptive cell', 0.42424242424242425, 3.6715585125471644, 1.2480508339450433, 'UPHENO:0086172', 'abnormal cell'),
(464881, 'HP:0031925', 'Rosette', 'XPO:0100509', 'abnormal germ plasm', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(464882, 'HP:0031925', 'Rosette', 'XPO:0128140', 'decreased size of the electrically active cell', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(464883, 'HP:0031925', 'Rosette', 'XPO:0100638', 'abnormal polar body', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(464884, 'HP:0031925', 'Rosette', 'XPO:0130973', 'abnormally increased number of stem cell', 0.42424242424242425, 3.6715585125471644, 1.2480508339450433, 'UPHENO:0086172', 'abnormal cell'),
(464885, 'HP:0031925', 'Rosette', 'XPO:0130871', 'increased size of the alkali secreting cell', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(464886, 'HP:0031925', 'Rosette', 'XPO:0127018', 'abnormally localised ciliated cell', 0.45161290322580644, 3.6715585125471644, 1.2876813267322194, 'UPHENO:0086172', 'abnormal cell'),
(464887, 'HP:0031925', 'Rosette', 'XPO:0101535', 'abnormal absorptive cell', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(464888, 'HP:0031925', 'Rosette', 'XPO:0102852', 'abnormal centriole morphology', 0.5333333333333333, 3.6715585125471644, 1.399344325041251, 'UPHENO:0086172', 'abnormal cell'),
(464889, 'HP:0031925', 'Rosette', 'XPO:0129156', 'decreased size of the oxygen accumulating cell', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(464890, 'HP:0031925', 'Rosette', 'XPO:0100901', 'abnormal blastomere D1.2.2', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(464891, 'HP:0031925', 'Rosette', 'XPO:0101657', 'abnormal oocyte morphology', 0.6, 5.43643956286526, 1.8060630492092893, 'HP:0025461', 'Abnormal cell morphology'),
(464892, 'HP:0031925', 'Rosette', 'XPO:0129623', 'increased size of the stem cell', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(464893, 'HP:0031925', 'Rosette', 'XPO:0102069', 'abnormal proepicardium morphology', 0.6, 5.43643956286526, 1.8060630492092893, 'HP:0025461', 'Abnormal cell morphology'),
(464894, 'HP:0031925', 'Rosette', 'XPO:0126738', 'abnormally localised paracrine cell', 0.45161290322580644, 3.6715585125471644, 1.2876813267322194, 'UPHENO:0086172', 'abnormal cell'),
(464895, 'HP:0031925', 'Rosette', 'XPO:0100967', 'abnormal blastomere V2.1.2', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(464896, 'HP:0031925', 'Rosette', 'XPO:0102281', 'abnormal growth cone morphology', 0.42105263157894735, 3.6715585125471644, 1.2433500608051093, 'UPHENO:0086172', 'abnormal cell'),
(464897, 'HP:0031925', 'Rosette', 'XPO:0100960', 'abnormal postmigratory neural crest cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(464898, 'HP:0031925', 'Rosette', 'XPO:0131629', 'increased size of the Roux spot', 0.43243243243243246, 3.6715585125471644, 1.2600400701560144, 'UPHENO:0086172', 'abnormal cell'),
(464899, 'HP:0031925', 'Rosette', 'XPO:0131531', 'absent cortical actin cytoskeleton', 0.4117647058823529, 3.6715585125471644, 1.229560169755361, 'UPHENO:0086172', 'abnormal cell'),
(464900, 'HP:0031925', 'Rosette', 'XPO:0131654', 'abnormal neuron projection', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(464901, 'HP:0031925', 'Rosette', 'XPO:0101269', 'abnormal mesodermal cell', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(464902, 'HP:0031925', 'Rosette', 'XPO:0130968', 'abnormally increased number of early embryonic cell', 0.4117647058823529, 3.6715585125471644, 1.229560169755361, 'UPHENO:0086172', 'abnormal cell'),
(464903, 'HP:0031925', 'Rosette', 'XPO:0102276', 'abnormal smooth muscle myocyte morphology', 0.4090909090909091, 5.43643956286526, 1.491307481034791, 'HP:0025461', 'Abnormal cell morphology'),
(464904, 'HP:0031925', 'Rosette', 'XPO:0100754', 'abnormal electrically active cell', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(464905, 'HP:0031925', 'Rosette', 'XPO:0129691', 'increased size of the progenitor cell', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(464906, 'HP:0031925', 'Rosette', 'XPO:0100225', 'abnormal endocrine system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(464907, 'HP:0031925', 'Rosette', 'XPO:0140733', 'abnormally necrotic T cell', 0.43902439024390244, 5.43643956286526, 1.5449043867452603, 'HP:0025461', 'Abnormal cell morphology'),
(464908, 'HP:0031925', 'Rosette', 'XPO:0126548', 'abnormally localised centrosome', 0.4375, 3.6715585125471644, 1.2674016132384338, 'UPHENO:0086172', 'abnormal cell'),
(464909, 'HP:0031925', 'Rosette', 'XPO:0129359', 'decreased size of the filopodium', 0.45714285714285713, 3.6715585125471644, 1.2955411026258445, 'UPHENO:0086172', 'abnormal cell'),
(464910, 'HP:0031925', 'Rosette', 'XPO:0127815', 'abnormally localised ciliated non-epidermal cell', 0.42424242424242425, 3.6715585125471644, 1.2480508339450433, 'UPHENO:0086172', 'abnormal cell'),
(464911, 'HP:0031925', 'Rosette', 'XPO:0130492', 'increased size of the spermatid', 0.4186046511627907, 5.43643956286526, 1.5085486027240909, 'HP:0025461', 'Abnormal cell morphology'),
(464912, 'HP:0031925', 'Rosette', 'XPO:0130632', 'increased size of the oxygen accumulating cell', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(464913, 'HP:0031925', 'Rosette', 'XPO:0131347', 'abnormally decreased number of myelin accumulating cell', 0.4117647058823529, 3.6715585125471644, 1.229560169755361, 'UPHENO:0086172', 'abnormal cell'),
(464914, 'HP:0031925', 'Rosette', 'XPO:0101504', 'abnormal blastomere D2.2.1', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(464915, 'HP:0031925', 'Rosette', 'XPO:0100715', 'abnormal ciliated cell', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(464916, 'HP:0031925', 'Rosette', 'XPO:0140381', 'abnormally necrotic ciliated cell', 0.5625, 5.43643956286526, 1.748713027947041, 'HP:0025461', 'Abnormal cell morphology'),
(464917, 'HP:0031925', 'Rosette', 'XPO:0129816', 'increased size of the proepicardium', 0.4186046511627907, 5.43643956286526, 1.5085486027240909, 'HP:0025461', 'Abnormal cell morphology'),
(464918, 'HP:0031925', 'Rosette', 'XPO:0100477', 'abnormal pericyte', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(464919, 'HP:0031925', 'Rosette', 'XPO:0141503', 'abnormal lymphoblast morphology', 0.5294117647058824, 5.43643956286526, 1.696500828969256, 'HP:0025461', 'Abnormal cell morphology'),
(464920, 'HP:0031925', 'Rosette', 'XPO:0140600', 'abnormally necrotic apoptotic cell', 0.5625, 5.43643956286526, 1.748713027947041, 'HP:0025461', 'Abnormal cell morphology'),
(464921, 'HP:0031925', 'Rosette', 'XPO:0102147', 'abnormal somatic stem cell morphology', 0.6, 5.43643956286526, 1.8060630492092893, 'HP:0025461', 'Abnormal cell morphology'),
(464922, 'HP:0031925', 'Rosette', 'XPO:0100308', 'abnormal early embryonic cell', 0.52, 3.6715585125471644, 1.3817418089225373, 'UPHENO:0086172', 'abnormal cell'),
(464923, 'HP:0031925', 'Rosette', 'XPO:0102896', 'abnormal mitotic spindle morphology', 0.5517241379310345, 3.6715585125471644, 1.423266473714053, 'UPHENO:0086172', 'abnormal cell'),
(464924, 'HP:0031925', 'Rosette', 'XPO:0131066', 'abnormally increased number of myoblast', 0.42424242424242425, 3.6715585125471644, 1.2480508339450433, 'UPHENO:0086172', 'abnormal cell'),
(464925, 'HP:0031925', 'Rosette', 'XPO:0101237', 'abnormal mucus secreting cell', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(464926, 'HP:0031925', 'Rosette', 'XPO:0101158', 'abnormal blastomere V2.2.2', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(464927, 'HP:0031925', 'Rosette', 'XPO:0140328', 'abnormally necrotic secondary oogonium', 0.5142857142857142, 5.43643956286526, 1.6720894724144628, 'HP:0025461', 'Abnormal cell morphology'),
(464928, 'HP:0031925', 'Rosette', 'XPO:0100004', 'abnormal cell', 0.5652173913043478, 3.6715585125471644, 1.440565418328227, 'UPHENO:0086172', 'abnormal cell'),
(464929, 'HP:0031925', 'Rosette', 'XPO:0130558', 'increased size of the multiciliated cell precursor', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(464930, 'HP:0031925', 'Rosette', 'XPO:0101740', 'abnormal cell part morphology', 0.5925925925925926, 3.6715585125471644, 1.4750384326537824, 'UPHENO:0086172', 'abnormal cell'),
(464931, 'HP:0031925', 'Rosette', 'XPO:0140752', 'abnormally necrotic melanoblast', 0.5625, 5.43643956286526, 1.748713027947041, 'HP:0025461', 'Abnormal cell morphology'),
(464932, 'HP:0031925', 'Rosette', 'XPO:0103100', 'abnormal stage I oocyte morphology', 0.5625, 5.43643956286526, 1.748713027947041, 'HP:0025461', 'Abnormal cell morphology'),
(464933, 'HP:0031925', 'Rosette', 'XPO:0103202', 'abnormal forelimb region morphology', 0.4444444444444444, 2.7446671847279203, 1.104469140402437, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(464934, 'HP:0031925', 'Rosette', 'XPO:0107346', 'abnormal animal-vegetal axis morphology', 0.4444444444444444, 2.7446671847279203, 1.104469140402437, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(464935, 'HP:0031925', 'Rosette', 'XPO:0100176', 'abnormal stage VI oocyte', 0.5, 3.6715585125471644, 1.3549093166236559, 'UPHENO:0086172', 'abnormal cell'),
(464936, 'HP:0031925', 'Rosette', 'XPO:0126454', 'abnormally localised stem cell', 0.45161290322580644, 3.6715585125471644, 1.2876813267322194, 'UPHENO:0086172', 'abnormal cell'),
(464937, 'HP:0031925', 'Rosette', 'XPO:0100336', 'abnormal interneuron', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(464938, 'HP:0031925', 'Rosette', 'XPO:0101461', 'abnormal sperm entry point', 0.5, 3.6715585125471644, 1.3549093166236559, 'UPHENO:0086172', 'abnormal cell'),
(464939, 'HP:0031925', 'Rosette', 'XPO:0101518', 'abnormal B cell', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(464940, 'HP:0031925', 'Rosette', 'XPO:0131607', 'decreased size of the cortical actin cytoskeleton', 0.4444444444444444, 3.6715585125471644, 1.2774207542365574, 'UPHENO:0086172', 'abnormal cell'),
(464941, 'HP:0031925', 'Rosette', 'XPO:0131550', 'abnormally localised adherens junction', 0.4375, 3.6715585125471644, 1.2674016132384338, 'UPHENO:0086172', 'abnormal cell'),
(464942, 'HP:0031925', 'Rosette', 'XPO:0101576', 'abnormal blastomere V1.2.2', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(464943, 'HP:0031925', 'Rosette', 'XPO:0139888', 'abnormally necrotic glial cell', 0.46153846153846156, 5.43643956286526, 1.5840220806831131, 'HP:0025461', 'Abnormal cell morphology'),
(464944, 'HP:0031925', 'Rosette', 'XPO:0130839', 'increased size of the absorptive cell', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(464945, 'HP:0031925', 'Rosette', 'XPO:0103083', 'abnormal dorsal lymph space morphology', 0.42424242424242425, 2.7446671847279203, 1.0790756508176813, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(464946, 'HP:0031925', 'Rosette', 'XPO:0141504', 'abnormal axon microtubule bundle morphology', 0.41025641025641024, 3.6715585125471644, 1.2273061620492112, 'UPHENO:0086172', 'abnormal cell'),
(464947, 'HP:0031925', 'Rosette', 'XPO:0131300', 'abnormally decreased number of alkali secreting cell', 0.4117647058823529, 3.6715585125471644, 1.229560169755361, 'UPHENO:0086172', 'abnormal cell'),
(464948, 'HP:0031925', 'Rosette', 'XPO:0101228', 'abnormal mesenchymal stem cell', 0.52, 3.6715585125471644, 1.3817418089225373, 'UPHENO:0086172', 'abnormal cell'),
(464949, 'HP:0031925', 'Rosette', 'XPO:0103167', 'abnormal absorptive cell morphology', 0.6428571428571429, 5.43643956286526, 1.869452862390249, 'HP:0025461', 'Abnormal cell morphology'),
(464950, 'HP:0031925', 'Rosette', 'XPO:0101409', 'abnormal perivitelline space', 0.5, 3.6715585125471644, 1.3549093166236559, 'UPHENO:0086172', 'abnormal cell'),
(464951, 'HP:0031925', 'Rosette', 'XPO:0102493', 'abnormal blastomere D2.2.2 morphology', 0.43902439024390244, 5.43643956286526, 1.5449043867452603, 'HP:0025461', 'Abnormal cell morphology'),
(464952, 'HP:0031925', 'Rosette', 'XPO:0128855', 'decreased size of the endoplasmic reticulum', 0.45714285714285713, 3.6715585125471644, 1.2955411026258445, 'UPHENO:0086172', 'abnormal cell'),
(464953, 'HP:0031925', 'Rosette', 'XPO:0102534', 'abnormal spermatocyte morphology', 0.6, 5.43643956286526, 1.8060630492092893, 'HP:0025461', 'Abnormal cell morphology'),
(464954, 'HP:0031925', 'Rosette', 'XPO:0103136', 'abnormal blastomere D2.2.1 morphology', 0.43902439024390244, 5.43643956286526, 1.5449043867452603, 'HP:0025461', 'Abnormal cell morphology'),
(464955, 'HP:0031925', 'Rosette', 'XPO:0128317', 'decreased size of the epithelial cell', 0.4186046511627907, 5.43643956286526, 1.5085486027240909, 'HP:0025461', 'Abnormal cell morphology'),
(464956, 'HP:0031925', 'Rosette', 'XPO:0102954', 'abnormal iridophore morphology', 0.4186046511627907, 5.43643956286526, 1.5085486027240909, 'HP:0025461', 'Abnormal cell morphology'),
(464957, 'HP:0031925', 'Rosette', 'XPO:0140471', 'abnormally necrotic multiciliated cell precursor', 0.5625, 5.43643956286526, 1.748713027947041, 'HP:0025461', 'Abnormal cell morphology'),
(464958, 'HP:0031925', 'Rosette', 'XPO:0125533', 'absent myelin accumulating cell', 0.42424242424242425, 3.6715585125471644, 1.2480508339450433, 'UPHENO:0086172', 'abnormal cell'),
(464959, 'HP:0031925', 'Rosette', 'XPO:0131090', 'abnormally increased number of oxygen accumulating cell', 0.42424242424242425, 3.6715585125471644, 1.2480508339450433, 'UPHENO:0086172', 'abnormal cell'),
(464960, 'HP:0031925', 'Rosette', 'XPO:0102109', 'abnormal pericyte morphology', 0.6428571428571429, 5.43643956286526, 1.869452862390249, 'HP:0025461', 'Abnormal cell morphology'),
(464961, 'HP:0031925', 'Rosette', 'XPO:0100189', 'abnormal enteroendocrine cell', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(464962, 'HP:0031925', 'Rosette', 'XPO:0140393', 'abnormally necrotic spermatocyte', 0.5142857142857142, 5.43643956286526, 1.6720894724144628, 'HP:0025461', 'Abnormal cell morphology'),
(464963, 'HP:0031925', 'Rosette', 'XPO:0102434', 'abnormal exocrine cell morphology', 0.6428571428571429, 5.43643956286526, 1.869452862390249, 'HP:0025461', 'Abnormal cell morphology'),
(464964, 'HP:0031925', 'Rosette', 'XPO:0101736', 'abnormal embryonic structure morphology', 0.42857142857142855, 2.7446671847279203, 1.0845671654222093, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(464965, 'HP:0031925', 'Rosette', 'XPO:0140927', 'abnormally necrotic basal region', 0.41379310344827586, 2.7446671847279203, 1.0657036887902793, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(464966, 'HP:0031925', 'Rosette', 'XPO:0102202', 'abnormal axon morphology', 0.41025641025641024, 3.6715585125471644, 1.2273061620492112, 'UPHENO:0086172', 'abnormal cell'),
(464967, 'HP:0031925', 'Rosette', 'XPO:0100415', 'abnormal secretory epithelial cell', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(464968, 'HP:0031925', 'Rosette', 'XPO:0107284', 'abnormal migrating myoblast', 0.52, 3.6715585125471644, 1.3817418089225373, 'UPHENO:0086172', 'abnormal cell'),
(464969, 'HP:0031925', 'Rosette', 'XPO:0127522', 'abnormally localised cementoblast', 0.45161290322580644, 3.6715585125471644, 1.2876813267322194, 'UPHENO:0086172', 'abnormal cell'),
(464970, 'HP:0031925', 'Rosette', 'XPO:0126982', 'abnormally localised secondary oogonium', 0.42424242424242425, 3.6715585125471644, 1.2480508339450433, 'UPHENO:0086172', 'abnormal cell'),
(464971, 'HP:0031925', 'Rosette', 'XPO:0124984', 'absent progenitor cell', 0.42424242424242425, 3.6715585125471644, 1.2480508339450433, 'UPHENO:0086172', 'abnormal cell'),
(464972, 'HP:0031925', 'Rosette', 'XPO:0101694', 'abnormal anatomical space morphology', 0.48, 2.7446671847279203, 1.1477979999413668, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(464973, 'HP:0031925', 'Rosette', 'XPO:0103043', 'abnormal marginal zone (sensu neural) morphology', 0.4444444444444444, 2.7446671847279203, 1.104469140402437, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(464974, 'HP:0031925', 'Rosette', 'XPO:0139780', 'abnormally necrotic neuron', 0.46153846153846156, 5.43643956286526, 1.5840220806831131, 'HP:0025461', 'Abnormal cell morphology'),
(464975, 'HP:0031925', 'Rosette', 'XPO:0127160', 'abnormally localised acid secreting cell', 0.45161290322580644, 3.6715585125471644, 1.2876813267322194, 'UPHENO:0086172', 'abnormal cell'),
(464976, 'HP:0031925', 'Rosette', 'XPO:0102526', 'abnormal nucleus morphology', 0.5517241379310345, 3.6715585125471644, 1.423266473714053, 'UPHENO:0086172', 'abnormal cell'),
(464977, 'HP:0031925', 'Rosette', 'XPO:0103631', 'abnormally increased number of apoptotic cell', 0.42424242424242425, 3.6715585125471644, 1.2480508339450433, 'UPHENO:0086172', 'abnormal cell'),
(464978, 'HP:0031925', 'Rosette', 'XPO:0131389', 'abnormally decreased number of barrier epithelial cell', 0.4117647058823529, 3.6715585125471644, 1.229560169755361, 'UPHENO:0086172', 'abnormal cell'),
(464979, 'HP:0031925', 'Rosette', 'XPO:0102297', 'abnormal egg jelly morphology', 0.42857142857142855, 2.7446671847279203, 1.0845671654222093, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(464980, 'HP:0031925', 'Rosette', 'XPO:0100026', 'abnormal germ cell', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(464981, 'HP:0031925', 'Rosette', 'XPO:0116091', 'abnormally increased variability of size of cell in endoderm', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(464982, 'HP:0031925', 'Rosette', 'XPO:0103006', 'abnormal migratory neural crest cell morphology', 0.43902439024390244, 5.43643956286526, 1.5449043867452603, 'HP:0025461', 'Abnormal cell morphology'),
(464983, 'HP:0031925', 'Rosette', 'XPO:0130333', 'increased size of the endoplasmic reticulum', 0.45714285714285713, 3.6715585125471644, 1.2955411026258445, 'UPHENO:0086172', 'abnormal cell'),
(464984, 'HP:0031925', 'Rosette', 'XPO:0129476', 'decreased size of the wedge region', 0.43243243243243246, 3.6715585125471644, 1.2600400701560144, 'UPHENO:0086172', 'abnormal cell'),
(464985, 'HP:0031925', 'Rosette', 'XPO:0101939', 'abnormal blastomere morphology', 0.5625, 5.43643956286526, 1.748713027947041, 'HP:0025461', 'Abnormal cell morphology'),
(464986, 'HP:0031925', 'Rosette', 'XPO:0130986', 'abnormally increased number of germ cell', 0.42424242424242425, 3.6715585125471644, 1.2480508339450433, 'UPHENO:0086172', 'abnormal cell'),
(464987, 'HP:0031925', 'Rosette', 'XPO:0140046', 'abnormally necrotic vitelline membrane', 0.42105263157894735, 3.6715585125471644, 1.2433500608051093, 'UPHENO:0086172', 'abnormal cell'),
(464988, 'HP:0031925', 'Rosette', 'XPO:0100649', 'abnormal growth cone', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(464989, 'HP:0031925', 'Rosette', 'XPO:0140239', 'abnormally necrotic absorptive cell', 0.5625, 5.43643956286526, 1.748713027947041, 'HP:0025461', 'Abnormal cell morphology'),
(464990, 'HP:0031925', 'Rosette', 'XPO:0102648', 'abnormal egg morphology', 0.43902439024390244, 5.43643956286526, 1.5449043867452603, 'HP:0025461', 'Abnormal cell morphology'),
(464991, 'HP:0031925', 'Rosette', 'XPO:0102496', 'abnormal dorsolateral ascending neuron morphology', 0.4864864864864865, 5.43643956286526, 1.626270082715184, 'HP:0025461', 'Abnormal cell morphology'),
(464992, 'HP:0031925', 'Rosette', 'XPO:0140522', 'abnormally necrotic stage II oocyte', 0.47368421052631576, 5.43643956286526, 1.6047291305419304, 'HP:0025461', 'Abnormal cell morphology'),
(464993, 'HP:0031925', 'Rosette', 'XPO:0102334', 'abnormal glial cell morphology', 0.5142857142857142, 5.43643956286526, 1.6720894724144628, 'HP:0025461', 'Abnormal cell morphology'),
(464994, 'HP:0031925', 'Rosette', 'XPO:0100965', 'abnormal blastomere V2.2', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(464995, 'HP:0031925', 'Rosette', 'XPO:0141165', 'abnormally necrotic ventral region', 0.42857142857142855, 2.7446671847279203, 1.0845671654222093, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(464996, 'HP:0031925', 'Rosette', 'XPO:0102446', 'abnormal natural killer cell morphology', 0.47368421052631576, 5.43643956286526, 1.6047291305419304, 'HP:0025461', 'Abnormal cell morphology'),
(464997, 'HP:0031925', 'Rosette', 'XPO:0125160', 'absent exocrine cell', 0.42424242424242425, 3.6715585125471644, 1.2480508339450433, 'UPHENO:0086172', 'abnormal cell'),
(464998, 'HP:0031925', 'Rosette', 'XPO:0101658', 'abnormal germ cell morphology', 0.6428571428571429, 5.43643956286526, 1.869452862390249, 'HP:0025461', 'Abnormal cell morphology'),
(464999, 'HP:0031925', 'Rosette', 'XPO:0140068', 'abnormally necrotic myoblast', 0.5625, 5.43643956286526, 1.748713027947041, 'HP:0025461', 'Abnormal cell morphology'),
(465000, 'HP:0031925', 'Rosette', 'XPO:0128547', 'decreased size of the zygote cortex', 0.4444444444444444, 3.6715585125471644, 1.2774207542365574, 'UPHENO:0086172', 'abnormal cell'),
(465001, 'HP:0031925', 'Rosette', 'XPO:0129797', 'increased size of the epithelial cell', 0.4186046511627907, 5.43643956286526, 1.5085486027240909, 'HP:0025461', 'Abnormal cell morphology'),
(465002, 'HP:0031925', 'Rosette', 'XPO:0142057', 'abnormal desmosome', 0.52, 3.6715585125471644, 1.3817418089225373, 'UPHENO:0086172', 'abnormal cell'),
(465003, 'HP:0031925', 'Rosette', 'XPO:0131635', 'increased size of the spindle microtubule', 0.42105263157894735, 3.6715585125471644, 1.2433500608051093, 'UPHENO:0086172', 'abnormal cell'),
(465004, 'HP:0031925', 'Rosette', 'XPO:0133438', 'abnormal cilium morphology in the ciliated non-epidermal cell', 0.5, 3.6715585125471644, 1.3549093166236559, 'UPHENO:0086172', 'abnormal cell'),
(465005, 'HP:0031925', 'Rosette', 'XPO:0125750', 'absent melanoblast', 0.42424242424242425, 3.6715585125471644, 1.2480508339450433, 'UPHENO:0086172', 'abnormal cell'),
(465006, 'HP:0031925', 'Rosette', 'XPO:0140267', 'abnormally necrotic multiciliated cell', 0.5142857142857142, 5.43643956286526, 1.6720894724144628, 'HP:0025461', 'Abnormal cell morphology'),
(465007, 'HP:0031925', 'Rosette', 'XPO:0131205', 'abnormally decreased number of ciliated cell', 0.4117647058823529, 3.6715585125471644, 1.229560169755361, 'UPHENO:0086172', 'abnormal cell'),
(465008, 'HP:0031925', 'Rosette', 'XPO:0130277', 'increased size of the cilium', 0.4444444444444444, 3.6715585125471644, 1.2774207542365574, 'UPHENO:0086172', 'abnormal cell'),
(465009, 'HP:0031925', 'Rosette', 'XPO:0102504', 'abnormal neuroendocrine cell morphology', 0.4864864864864865, 5.43643956286526, 1.626270082715184, 'HP:0025461', 'Abnormal cell morphology'),
(465010, 'HP:0031925', 'Rosette', 'XPO:0141285', 'abnormal cortical actin cytoskeleton morphology', 0.5333333333333333, 3.6715585125471644, 1.399344325041251, 'UPHENO:0086172', 'abnormal cell'),
(465011, 'HP:0031925', 'Rosette', 'XPO:0126628', 'abnormally localised blastomere', 0.4117647058823529, 3.6715585125471644, 1.229560169755361, 'UPHENO:0086172', 'abnormal cell'),
(465012, 'HP:0031925', 'Rosette', 'XPO:0103037', 'abnormal ring structure morphology', 0.5161290322580645, 3.6715585125471644, 1.376589242279565, 'UPHENO:0086172', 'abnormal cell'),
(465013, 'HP:0031925', 'Rosette', 'XPO:0107350', 'abnormal anatomical side morphology', 0.4444444444444444, 2.7446671847279203, 1.104469140402437, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(465014, 'HP:0031925', 'Rosette', 'XPO:0102475', 'abnormal fasciculated network of fibrils morphology', 0.4444444444444444, 3.6715585125471644, 1.2774207542365574, 'UPHENO:0086172', 'abnormal cell'),
(465015, 'HP:0031925', 'Rosette', 'XPO:0100872', 'abnormal neuroendocrine cell', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(465016, 'HP:0031925', 'Rosette', 'XPO:0131195', 'abnormally decreased number of Merkel cell', 0.4117647058823529, 3.6715585125471644, 1.229560169755361, 'UPHENO:0086172', 'abnormal cell'),
(465017, 'HP:0031925', 'Rosette', 'XPO:0107399', 'abnormal filopodium morphology', 0.5517241379310345, 3.6715585125471644, 1.423266473714053, 'UPHENO:0086172', 'abnormal cell'),
(465018, 'HP:0031925', 'Rosette', 'XPO:0102693', 'abnormal plasma membrane morphology', 0.5517241379310345, 3.6715585125471644, 1.423266473714053, 'UPHENO:0086172', 'abnormal cell'),
(465019, 'HP:0031925', 'Rosette', 'XPO:0126495', 'abnormally localised keratin accumulating cell', 0.45161290322580644, 3.6715585125471644, 1.2876813267322194, 'UPHENO:0086172', 'abnormal cell'),
(465020, 'HP:0031925', 'Rosette', 'XPO:0125724', 'absent polar body', 0.4117647058823529, 3.6715585125471644, 1.229560169755361, 'UPHENO:0086172', 'abnormal cell'),
(465021, 'HP:0031925', 'Rosette', 'XPO:0125644', 'absent pericyte', 0.42424242424242425, 3.6715585125471644, 1.2480508339450433, 'UPHENO:0086172', 'abnormal cell'),
(465022, 'HP:0031925', 'Rosette', 'XPO:0102181', 'abnormal mitotic cell morphology', 0.6428571428571429, 5.43643956286526, 1.869452862390249, 'HP:0025461', 'Abnormal cell morphology'),
(465023, 'HP:0031925', 'Rosette', 'XPO:0101136', 'abnormal ooplasm', 0.48148148148148145, 3.6715585125471644, 1.3295816755533123, 'UPHENO:0086172', 'abnormal cell'),
(465024, 'HP:0031925', 'Rosette', 'XPO:0141254', 'abnormally necrotic dorso-lateral region', 0.42857142857142855, 2.7446671847279203, 1.0845671654222093, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(465025, 'HP:0031925', 'Rosette', 'XPO:0128307', 'decreased size of the oocyte', 0.4186046511627907, 5.43643956286526, 1.5085486027240909, 'HP:0025461', 'Abnormal cell morphology'),
(465026, 'HP:0031925', 'Rosette', 'XPO:0128091', 'decreased size of the anatomical region', 0.41379310344827586, 2.7446671847279203, 1.0657036887902793, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(465027, 'HP:0031925', 'Rosette', 'XPO:0126214', 'absent microtubule', 0.42424242424242425, 3.6715585125471644, 1.2480508339450433, 'UPHENO:0086172', 'abnormal cell'),
(465028, 'HP:0031925', 'Rosette', 'XPO:0100674', 'abnormal secondary oogonium', 0.52, 3.6715585125471644, 1.3817418089225373, 'UPHENO:0086172', 'abnormal cell'),
(465029, 'HP:0031925', 'Rosette', 'XPO:0100899', 'abnormal secondary spermatogonium', 0.52, 3.6715585125471644, 1.3817418089225373, 'UPHENO:0086172', 'abnormal cell'),
(465030, 'HP:0031925', 'Rosette', 'XPO:0101948', 'abnormal gamete morphology', 0.46153846153846156, 5.43643956286526, 1.5840220806831131, 'HP:0025461', 'Abnormal cell morphology'),
(465031, 'HP:0031925', 'Rosette', 'XPO:0100335', 'abnormal commissural interneuron', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(465032, 'HP:0031925', 'Rosette', 'XPO:0129397', 'decreased size of the alkali secreting cell', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(465033, 'HP:0031925', 'Rosette', 'XPO:0101485', 'abnormal descending interneuron', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(465034, 'HP:0031925', 'Rosette', 'XPO:0103927', 'decreased pigmentation in the whole organism', 0.42857142857142855, 2.7446671847279203, 1.0845671654222093, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(465035, 'HP:0031925', 'Rosette', 'XPO:0103219', 'abnormal hemangioblast morphology', 0.5294117647058824, 5.43643956286526, 1.696500828969256, 'HP:0025461', 'Abnormal cell morphology'),
(465036, 'HP:0031925', 'Rosette', 'XPO:0100289', 'abnormal chondroblast', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(465037, 'HP:0031925', 'Rosette', 'XPO:0139891', 'abnormally necrotic myocyte', 0.4090909090909091, 5.43643956286526, 1.491307481034791, 'HP:0025461', 'Abnormal cell morphology'),
(465038, 'HP:0031925', 'Rosette', 'XPO:0141197', 'abnormally necrotic mesodermal cell', 0.42857142857142855, 5.43643956286526, 1.526401870347189, 'HP:0025461', 'Abnormal cell morphology'),
(465039, 'HP:0031925', 'Rosette', 'XPO:0142067', 'abnormally necrotic desmosome', 0.5, 3.6715585125471644, 1.3549093166236559, 'UPHENO:0086172', 'abnormal cell'),
(465040, 'HP:0031925', 'Rosette', 'XPO:0100888', 'abnormal microtubule', 0.52, 3.6715585125471644, 1.3817418089225373, 'UPHENO:0086172', 'abnormal cell'),
(465041, 'HP:0031925', 'Rosette', 'XPO:0102009', 'abnormal connective tissue morphology', 0.42424242424242425, 2.7446671847279203, 1.0790756508176813, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(465042, 'HP:0031925', 'Rosette', 'XPO:0102153', 'abnormal animal blastomere morphology', 0.4864864864864865, 5.43643956286526, 1.626270082715184, 'HP:0025461', 'Abnormal cell morphology'),
(465043, 'HP:0031925', 'Rosette', 'XPO:0131687', 'abnormal astral microtubule', 0.48148148148148145, 3.6715585125471644, 1.3295816755533123, 'UPHENO:0086172', 'abnormal cell'),
(465044, 'HP:0031925', 'Rosette', 'XPO:0100701', 'abnormal microglial cell', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(465045, 'HP:0031925', 'Rosette', 'XPO:0141146', 'abnormally necrotic oxygen accumulating cell', 0.5625, 5.43643956286526, 1.748713027947041, 'HP:0025461', 'Abnormal cell morphology'),
(465046, 'HP:0031925', 'Rosette', 'XPO:0140973', 'abnormally necrotic erythroid cell', 0.47368421052631576, 5.43643956286526, 1.6047291305419304, 'HP:0025461', 'Abnormal cell morphology'),
(465047, 'HP:0031925', 'Rosette', 'XPO:0141023', 'abnormally necrotic ciliated non-epidermal cell', 0.5142857142857142, 5.43643956286526, 1.6720894724144628, 'HP:0025461', 'Abnormal cell morphology'),
(465048, 'HP:0031925', 'Rosette', 'XPO:0102726', 'abnormal blastomere V2.2.1 morphology', 0.43902439024390244, 5.43643956286526, 1.5449043867452603, 'HP:0025461', 'Abnormal cell morphology'),
(465049, 'HP:0031925', 'Rosette', 'XPO:0102275', 'abnormal thoracic region morphology', 0.4444444444444444, 2.7446671847279203, 1.104469140402437, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(465050, 'HP:0031925', 'Rosette', 'XPO:0100864', 'abnormal dorsolateral ascending neuron', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(465051, 'HP:0031925', 'Rosette', 'XPO:0140747', 'abnormally necrotic morula cell', 0.4864864864864865, 5.43643956286526, 1.626270082715184, 'HP:0025461', 'Abnormal cell morphology'),
(465052, 'HP:0031925', 'Rosette', 'XPO:0127257', 'abnormally localised wedge region', 0.4117647058823529, 3.6715585125471644, 1.229560169755361, 'UPHENO:0086172', 'abnormal cell'),
(465053, 'HP:0031925', 'Rosette', 'XPO:0107286', 'abnormal efferent neuron', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(465054, 'HP:0031925', 'Rosette', 'XPO:0100900', 'abnormal angioblast', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(465055, 'HP:0031925', 'Rosette', 'XPO:0125779', 'absent endoplasmic reticulum', 0.42424242424242425, 3.6715585125471644, 1.2480508339450433, 'UPHENO:0086172', 'abnormal cell'),
(465056, 'HP:0031925', 'Rosette', 'XPO:0131283', 'abnormally decreased number of myoblast', 0.4117647058823529, 3.6715585125471644, 1.229560169755361, 'UPHENO:0086172', 'abnormal cell'),
(465057, 'HP:0031925', 'Rosette', 'XPO:0107349', 'abnormal left-right axis morphology', 0.4444444444444444, 2.7446671847279203, 1.104469140402437, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(465058, 'HP:0031925', 'Rosette', 'XPO:0107348', 'abnormal dorsal-ventral axis morphology', 0.4444444444444444, 2.7446671847279203, 1.104469140402437, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(465059, 'HP:0031925', 'Rosette', 'XPO:0130850', 'increased size of the lampbrush chromosome', 0.45714285714285713, 3.6715585125471644, 1.2955411026258445, 'UPHENO:0086172', 'abnormal cell'),
(465060, 'HP:0031925', 'Rosette', 'XPO:0100956', 'abnormal centrosome', 0.52, 3.6715585125471644, 1.3817418089225373, 'UPHENO:0086172', 'abnormal cell'),
(465061, 'HP:0031925', 'Rosette', 'XPO:0102494', 'abnormal blastomere V1 morphology', 0.5294117647058824, 5.43643956286526, 1.696500828969256, 'HP:0025461', 'Abnormal cell morphology'),
(465062, 'HP:0031925', 'Rosette', 'XPO:0100317', 'abnormal respiratory system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(465063, 'HP:0031925', 'Rosette', 'XPO:0101168', 'abnormal circulating cell', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(465064, 'HP:0031925', 'Rosette', 'XPO:0100108', 'abnormal cell part', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(465065, 'HP:0031925', 'Rosette', 'XPO:0100501', 'abnormal urogenital system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(465066, 'HP:0031925', 'Rosette', 'XPO:0141478', 'abnormally necrotic lymphoblast', 0.47368421052631576, 5.43643956286526, 1.6047291305419304, 'HP:0025461', 'Abnormal cell morphology'),
(465067, 'HP:0031925', 'Rosette', 'XPO:0131666', 'abnormal adherens junction', 0.52, 3.6715585125471644, 1.3817418089225373, 'UPHENO:0086172', 'abnormal cell'),
(465068, 'HP:0031925', 'Rosette', 'XPO:0101435', 'abnormal paracrine cell', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(465069, 'HP:0031925', 'Rosette', 'XPO:0128911', 'decreased size of the barrier cell', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(465070, 'HP:0031925', 'Rosette', 'XPO:0125523', 'absent acid secreting cell', 0.42424242424242425, 3.6715585125471644, 1.2480508339450433, 'UPHENO:0086172', 'abnormal cell'),
(465071, 'HP:0031925', 'Rosette', 'XPO:0131637', 'increased size of the actin filament', 0.4444444444444444, 3.6715585125471644, 1.2774207542365574, 'UPHENO:0086172', 'abnormal cell'),
(465072, 'HP:0031925', 'Rosette', 'XPO:0101713', 'abnormal anatomical entity in vitro morphology', 0.5217391304347826, 2.7446671847279203, 1.196662137068282, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(465073, 'HP:0031925', 'Rosette', 'XPO:0141112', 'abnormally necrotic angioblast', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(465074, 'HP:0031925', 'Rosette', 'XPO:0100861', 'abnormal blastomere D2.2.2', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(465075, 'HP:0031925', 'Rosette', 'XPO:0126159', 'absent apoptotic cell', 0.42424242424242425, 3.6715585125471644, 1.2480508339450433, 'UPHENO:0086172', 'abnormal cell'),
(465076, 'HP:0031925', 'Rosette', 'XPO:0129982', 'increased size of the anatomical line', 0.4444444444444444, 2.7446671847279203, 1.104469140402437, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(465077, 'HP:0031925', 'Rosette', 'XPO:0101374', 'abnormal migratory neural crest cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(465078, 'HP:0031925', 'Rosette', 'XPO:0140075', 'abnormally necrotic stem cell', 0.5625, 5.43643956286526, 1.748713027947041, 'HP:0025461', 'Abnormal cell morphology'),
(465079, 'HP:0031925', 'Rosette', 'XPO:0101094', 'abnormal blastomere V2.2.1', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(465080, 'HP:0031925', 'Rosette', 'XPO:0139951', 'abnormally necrotic lymphocyte', 0.47368421052631576, 5.43643956286526, 1.6047291305419304, 'HP:0025461', 'Abnormal cell morphology'),
(465081, 'HP:0031925', 'Rosette', 'XPO:0130439', 'increased size of the Merkel cell', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(465082, 'HP:0031925', 'Rosette', 'XPO:0130732', 'increased size of the mitotic spindle', 0.45714285714285713, 3.6715585125471644, 1.2955411026258445, 'UPHENO:0086172', 'abnormal cell'),
(465083, 'HP:0031925', 'Rosette', 'XPO:0100265', 'abnormal sensory epithelial cell', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(465084, 'HP:0031925', 'Rosette', 'XPO:0125692', 'absent oxygen accumulating cell', 0.42424242424242425, 3.6715585125471644, 1.2480508339450433, 'UPHENO:0086172', 'abnormal cell'),
(465085, 'HP:0031925', 'Rosette', 'XPO:0100398', 'abnormal vegetal blastomere', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(465086, 'HP:0031925', 'Rosette', 'XPO:0102152', 'abnormal blastomere D1.2 morphology', 0.43902439024390244, 5.43643956286526, 1.5449043867452603, 'HP:0025461', 'Abnormal cell morphology'),
(465087, 'HP:0031925', 'Rosette', 'XPO:0128143', 'decreased size of the stem cell', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(465088, 'HP:0031925', 'Rosette', 'XPO:0141505', 'abnormal tadpole morphology', 0.4444444444444444, 2.7446671847279203, 1.104469140402437, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(465089, 'HP:0031925', 'Rosette', 'XPO:0127171', 'abnormally localised myelin accumulating cell', 0.45161290322580644, 3.6715585125471644, 1.2876813267322194, 'UPHENO:0086172', 'abnormal cell'),
(465090, 'HP:0031925', 'Rosette', 'XPO:0102798', 'abnormal premigratory neural crest cell morphology', 0.43902439024390244, 5.43643956286526, 1.5449043867452603, 'HP:0025461', 'Abnormal cell morphology'),
(465091, 'HP:0031925', 'Rosette', 'XPO:0100917', 'abnormal stage III oocyte', 0.5, 3.6715585125471644, 1.3549093166236559, 'UPHENO:0086172', 'abnormal cell'),
(465092, 'HP:0031925', 'Rosette', 'XPO:0100814', 'abnormal natural killer cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(465093, 'HP:0031925', 'Rosette', 'XPO:0101702', 'abnormal anatomical system morphology', 0.42857142857142855, 2.7446671847279203, 1.0845671654222093, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(465094, 'HP:0031925', 'Rosette', 'XPO:0141296', 'abnormal adherens junction morphology', 0.5517241379310345, 3.6715585125471644, 1.423266473714053, 'UPHENO:0086172', 'abnormal cell'),
(465095, 'HP:0031925', 'Rosette', 'XPO:0102556', 'abnormal spermatozoon morphology', 0.43902439024390244, 5.43643956286526, 1.5449043867452603, 'HP:0025461', 'Abnormal cell morphology'),
(465096, 'HP:0031925', 'Rosette', 'XPO:0127337', 'abnormally localised oxygen accumulating cell', 0.45161290322580644, 3.6715585125471644, 1.2876813267322194, 'UPHENO:0086172', 'abnormal cell'),
(465097, 'HP:0031925', 'Rosette', 'XPO:0100218', 'abnormal epithelial cell', 0.48148148148148145, 3.6715585125471644, 1.3295816755533123, 'UPHENO:0086172', 'abnormal cell'),
(465098, 'HP:0031925', 'Rosette', 'XPO:0130912', 'increased size of the mitotic cell', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(465099, 'HP:0031925', 'Rosette', 'XPO:0131348', 'abnormally decreased number of absorptive cell', 0.4117647058823529, 3.6715585125471644, 1.229560169755361, 'UPHENO:0086172', 'abnormal cell'),
(465100, 'HP:0031925', 'Rosette', 'XPO:0129747', 'increased size of the zygote', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(465101, 'HP:0031925', 'Rosette', 'XPO:0129365', 'decreased size of the absorptive cell', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(465102, 'HP:0031925', 'Rosette', 'XPO:0100521', 'abnormal animal blastomere', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(465103, 'HP:0031925', 'Rosette', 'XPO:0131551', 'abnormally localised actin cytoskeleton', 0.4375, 3.6715585125471644, 1.2674016132384338, 'UPHENO:0086172', 'abnormal cell'),
(465104, 'HP:0031925', 'Rosette', 'XPO:0141087', 'abnormally necrotic right-dorsal blastomere', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(465105, 'HP:0031925', 'Rosette', 'XPO:0103098', 'abnormal secondary myofiber morphology', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(465106, 'HP:0031925', 'Rosette', 'XPO:0129256', 'decreased size of the mitotic spindle', 0.45714285714285713, 3.6715585125471644, 1.2955411026258445, 'UPHENO:0086172', 'abnormal cell'),
(465107, 'HP:0031925', 'Rosette', 'XPO:0127338', 'abnormally localised mucus secreting cell', 0.45161290322580644, 3.6715585125471644, 1.2876813267322194, 'UPHENO:0086172', 'abnormal cell'),
(465108, 'HP:0031925', 'Rosette', 'XPO:0101864', 'abnormal lymphatic system morphology', 0.42424242424242425, 2.7446671847279203, 1.0790756508176813, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(465109, 'HP:0031925', 'Rosette', 'XPO:0102347', 'abnormal ciliated cell morphology', 0.6428571428571429, 5.43643956286526, 1.869452862390249, 'HP:0025461', 'Abnormal cell morphology'),
(465110, 'HP:0031925', 'Rosette', 'XPO:0102520', 'abnormal microtubule morphology', 0.5517241379310345, 3.6715585125471644, 1.423266473714053, 'UPHENO:0086172', 'abnormal cell'),
(465111, 'HP:0031925', 'Rosette', 'XPO:0102860', 'abnormal mesenchymal stem cell morphology', 0.6, 5.43643956286526, 1.8060630492092893, 'HP:0025461', 'Abnormal cell morphology'),
(465112, 'HP:0031925', 'Rosette', 'XPO:0102832', 'abnormal joint region morphology', 0.4444444444444444, 2.7446671847279203, 1.104469140402437, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(465113, 'HP:0031925', 'Rosette', 'XPO:0127508', 'abnormally localised barrier epithelial cell', 0.45161290322580644, 3.6715585125471644, 1.2876813267322194, 'UPHENO:0086172', 'abnormal cell'),
(465114, 'HP:0031925', 'Rosette', 'XPO:0128734', 'decreased size of the spermatocyte', 0.4186046511627907, 5.43643956286526, 1.5085486027240909, 'HP:0025461', 'Abnormal cell morphology'),
(465115, 'HP:0031925', 'Rosette', 'XPO:0102364', 'abnormal tendon fibroblast morphology', 0.42857142857142855, 5.43643956286526, 1.526401870347189, 'HP:0025461', 'Abnormal cell morphology'),
(465116, 'HP:0031925', 'Rosette', 'XPO:0131561', 'abnormally localised actin filament', 0.42424242424242425, 3.6715585125471644, 1.2480508339450433, 'UPHENO:0086172', 'abnormal cell'),
(465117, 'HP:0031925', 'Rosette', 'XPO:0100989', 'abnormal right blastomere', 0.48148148148148145, 3.6715585125471644, 1.3295816755533123, 'UPHENO:0086172', 'abnormal cell'),
(465118, 'HP:0031925', 'Rosette', 'XPO:0101302', 'abnormal subcortical cytoplasm', 0.48148148148148145, 3.6715585125471644, 1.3295816755533123, 'UPHENO:0086172', 'abnormal cell'),
(465119, 'HP:0031925', 'Rosette', 'XPO:0128211', 'decreased size of the progenitor cell', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(465120, 'HP:0031925', 'Rosette', 'XPO:0139717', 'abnormally necrotic cell', 0.6206896551724138, 5.43643956286526, 1.8369381583604023, 'HP:0025461', 'Abnormal cell morphology'),
(465121, 'HP:0031925', 'Rosette', 'XPO:0131513', 'absent actin cytoskeleton', 0.42424242424242425, 3.6715585125471644, 1.2480508339450433, 'UPHENO:0086172', 'abnormal cell'),
(465122, 'HP:0031925', 'Rosette', 'XPO:0101635', 'abnormal organism subdivision morphology', 0.42857142857142855, 2.7446671847279203, 1.0845671654222093, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(465123, 'HP:0031925', 'Rosette', 'XPO:0128156', 'decreased size of the chondroblast', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(465124, 'HP:0031925', 'Rosette', 'XPO:0141239', 'abnormally necrotic neural progenitor cell', 0.42857142857142855, 5.43643956286526, 1.526401870347189, 'HP:0025461', 'Abnormal cell morphology'),
(465125, 'HP:0031925', 'Rosette', 'XPO:0140144', 'abnormally necrotic portion of organism substance', 0.48, 2.7446671847279203, 1.1477979999413668, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(465126, 'HP:0031925', 'Rosette', 'XPO:0100894', 'abnormal nucleus', 0.52, 3.6715585125471644, 1.3817418089225373, 'UPHENO:0086172', 'abnormal cell'),
(465127, 'HP:0031925', 'Rosette', 'XPO:0102179', 'abnormal blastomere V2 morphology', 0.5294117647058824, 5.43643956286526, 1.696500828969256, 'HP:0025461', 'Abnormal cell morphology'),
(465128, 'HP:0031925', 'Rosette', 'XPO:0127824', 'abnormally localised alkali secreting cell', 0.45161290322580644, 3.6715585125471644, 1.2876813267322194, 'UPHENO:0086172', 'abnormal cell'),
(465129, 'HP:0031925', 'Rosette', 'XPO:0139929', 'abnormally necrotic barrier epithelial cell', 0.5625, 5.43643956286526, 1.748713027947041, 'HP:0025461', 'Abnormal cell morphology'),
(465130, 'HP:0031925', 'Rosette', 'XPO:0127896', 'abnormally localised ring structure', 0.4117647058823529, 3.6715585125471644, 1.229560169755361, 'UPHENO:0086172', 'abnormal cell'),
(465131, 'HP:0031925', 'Rosette', 'XPO:0103067', 'abnormal paracrine cell morphology', 0.6428571428571429, 5.43643956286526, 1.869452862390249, 'HP:0025461', 'Abnormal cell morphology'),
(465132, 'HP:0031925', 'Rosette', 'XPO:0101022', 'abnormal blastomere V1.2', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(465133, 'HP:0031925', 'Rosette', 'XPO:0139992', 'abnormally necrotic gamete', 0.4090909090909091, 5.43643956286526, 1.491307481034791, 'HP:0025461', 'Abnormal cell morphology'),
(465134, 'HP:0031925', 'Rosette', 'XPO:0128799', 'decreased size of the cilium', 0.4444444444444444, 3.6715585125471644, 1.2774207542365574, 'UPHENO:0086172', 'abnormal cell'),
(465135, 'HP:0031925', 'Rosette', 'XPO:0103099', 'abnormal alkali secreting cell morphology', 0.6428571428571429, 5.43643956286526, 1.869452862390249, 'HP:0025461', 'Abnormal cell morphology'),
(465136, 'HP:0031925', 'Rosette', 'XPO:0125698', 'absent filopodium', 0.42424242424242425, 3.6715585125471644, 1.2480508339450433, 'UPHENO:0086172', 'abnormal cell'),
(465137, 'HP:0031925', 'Rosette', 'XPO:0101083', 'abnormal T cell', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(465138, 'HP:0031925', 'Rosette', 'XPO:0102549', 'abnormal stage III oocyte morphology', 0.5625, 5.43643956286526, 1.748713027947041, 'HP:0025461', 'Abnormal cell morphology'),
(465139, 'HP:0031925', 'Rosette', 'XPO:0102958', 'abnormal cementoblast morphology', 0.6428571428571429, 5.43643956286526, 1.869452862390249, 'HP:0025461', 'Abnormal cell morphology'),
(465140, 'HP:0031925', 'Rosette', 'XPO:0139901', 'abnormally necrotic enteroendocrine cell', 0.42857142857142855, 5.43643956286526, 1.526401870347189, 'HP:0025461', 'Abnormal cell morphology'),
(465141, 'HP:0031925', 'Rosette', 'XPO:0102024', 'abnormal cilium morphology', 0.5333333333333333, 3.6715585125471644, 1.399344325041251, 'UPHENO:0086172', 'abnormal cell'),
(465142, 'HP:0031925', 'Rosette', 'XPO:0141054', 'abnormally necrotic ectodermal cell', 0.42857142857142855, 5.43643956286526, 1.526401870347189, 'HP:0025461', 'Abnormal cell morphology'),
(465143, 'HP:0031925', 'Rosette', 'XPO:0100547', 'abnormal blastomere V2', 0.48148148148148145, 3.6715585125471644, 1.3295816755533123, 'UPHENO:0086172', 'abnormal cell'),
(465144, 'HP:0031925', 'Rosette', 'XPO:0101857', 'abnormal endocrine system morphology', 0.4117647058823529, 2.7446671847279203, 1.0630884610720022, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(465145, 'HP:0031925', 'Rosette', 'XPO:0101345', 'abnormal ascending interneuron', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(465146, 'HP:0031925', 'Rosette', 'XPO:0127653', 'abnormally localised Merkel cell', 0.45161290322580644, 3.6715585125471644, 1.2876813267322194, 'UPHENO:0086172', 'abnormal cell'),
(465147, 'HP:0031925', 'Rosette', 'XPO:0130964', 'abnormally increased number of cell', 0.45161290322580644, 3.6715585125471644, 1.2876813267322194, 'UPHENO:0086172', 'abnormal cell'),
(465148, 'HP:0031925', 'Rosette', 'XPO:0101494', 'abnormal blastomere D1.2.1', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(465149, 'HP:0031925', 'Rosette', 'XPO:0141241', 'abnormally necrotic olfactory epithelial support cell', 0.42857142857142855, 5.43643956286526, 1.526401870347189, 'HP:0025461', 'Abnormal cell morphology'),
(465150, 'HP:0031925', 'Rosette', 'XPO:0101467', 'abnormal alkali secreting cell', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(465151, 'HP:0031925', 'Rosette', 'XPO:0102800', 'abnormal circulating cell morphology', 0.5, 5.43643956286526, 1.6487024538808177, 'HP:0025461', 'Abnormal cell morphology'),
(465152, 'HP:0031925', 'Rosette', 'XPO:0127876', 'abnormally localised microtubule', 0.4375, 3.6715585125471644, 1.2674016132384338, 'UPHENO:0086172', 'abnormal cell'),
(465153, 'HP:0031925', 'Rosette', 'XPO:0102871', 'abnormal olfactory epithelial support cell morphology', 0.47368421052631576, 5.43643956286526, 1.6047291305419304, 'HP:0025461', 'Abnormal cell morphology'),
(465154, 'HP:0031925', 'Rosette', 'XPO:0127343', 'abnormally localised filopodium', 0.4375, 3.6715585125471644, 1.2674016132384338, 'UPHENO:0086172', 'abnormal cell'),
(465155, 'HP:0031925', 'Rosette', 'XPO:0102765', 'abnormal motor neuron morphology', 0.4864864864864865, 5.43643956286526, 1.626270082715184, 'HP:0025461', 'Abnormal cell morphology'),
(465156, 'HP:0031925', 'Rosette', 'XPO:0101808', 'abnormal stage VI oocyte morphology', 0.5625, 5.43643956286526, 1.748713027947041, 'HP:0025461', 'Abnormal cell morphology'),
(465157, 'HP:0031925', 'Rosette', 'XPO:0139758', 'abnormally necrotic oocyte', 0.5142857142857142, 5.43643956286526, 1.6720894724144628, 'HP:0025461', 'Abnormal cell morphology'),
(465158, 'HP:0031925', 'Rosette', 'XPO:0103080', 'abnormal myelin accumulating cell morphology', 0.6428571428571429, 5.43643956286526, 1.869452862390249, 'HP:0025461', 'Abnormal cell morphology'),
(465159, 'HP:0031925', 'Rosette', 'XPO:0139969', 'abnormally necrotic primordial germ cell', 0.5142857142857142, 5.43643956286526, 1.6720894724144628, 'HP:0025461', 'Abnormal cell morphology'),
(465160, 'HP:0031925', 'Rosette', 'XPO:0131247', 'abnormally decreased number of nucleate erythrocyte', 0.4117647058823529, 3.6715585125471644, 1.229560169755361, 'UPHENO:0086172', 'abnormal cell'),
(465161, 'HP:0031925', 'Rosette', 'XPO:0139839', 'abnormally necrotic progenitor cell', 0.5625, 5.43643956286526, 1.748713027947041, 'HP:0025461', 'Abnormal cell morphology'),
(465162, 'HP:0031925', 'Rosette', 'XPO:0127476', 'abnormally localised nucleus', 0.4375, 3.6715585125471644, 1.2674016132384338, 'UPHENO:0086172', 'abnormal cell'),
(465163, 'HP:0031925', 'Rosette', 'XPO:0140637', 'abnormally necrotic motor neuron', 0.42857142857142855, 5.43643956286526, 1.526401870347189, 'HP:0025461', 'Abnormal cell morphology'),
(465164, 'HP:0031925', 'Rosette', 'XPO:0101362', 'abnormal vegetal cortex', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(465165, 'HP:0031925', 'Rosette', 'XPO:0100653', 'abnormal myoblast', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(465166, 'HP:0031925', 'Rosette', 'XPO:0139995', 'abnormally necrotic neuroendocrine cell', 0.42857142857142855, 5.43643956286526, 1.526401870347189, 'HP:0025461', 'Abnormal cell morphology'),
(465167, 'HP:0031925', 'Rosette', 'XPO:0130258', 'increased size of the keratin accumulating cell', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(465168, 'HP:0031925', 'Rosette', 'XPO:0100843', 'abnormal fasciculated network of fibrils', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(465169, 'HP:0031925', 'Rosette', 'XPO:0103122', 'abnormal ectodermal cell morphology', 0.47368421052631576, 5.43643956286526, 1.6047291305419304, 'HP:0025461', 'Abnormal cell morphology'),
(465170, 'HP:0031925', 'Rosette', 'XPO:0101162', 'abnormal stromal cell', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(465171, 'HP:0031925', 'Rosette', 'XPO:0102608', 'abnormal multiciliated cell morphology', 0.6, 5.43643956286526, 1.8060630492092893, 'HP:0025461', 'Abnormal cell morphology'),
(465172, 'HP:0031925', 'Rosette', 'XPO:0100196', 'abnormal neuron', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(465173, 'HP:0031925', 'Rosette', 'XPO:0141189', 'abnormally necrotic antero-ventral region', 0.42857142857142855, 2.7446671847279203, 1.0845671654222093, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(465174, 'HP:0031925', 'Rosette', 'XPO:0128336', 'decreased size of the proepicardium', 0.4186046511627907, 5.43643956286526, 1.5085486027240909, 'HP:0025461', 'Abnormal cell morphology'),
(465175, 'HP:0031925', 'Rosette', 'XPO:0107345', 'abnormal anatomical axis morphology', 0.48, 2.7446671847279203, 1.1477979999413668, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(465176, 'HP:0031925', 'Rosette', 'XPO:0140767', 'abnormally necrotic stage IV oocyte', 0.47368421052631576, 5.43643956286526, 1.6047291305419304, 'HP:0025461', 'Abnormal cell morphology'),
(465177, 'HP:0031925', 'Rosette', 'XPO:0100258', 'abnormal organ part', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(465178, 'HP:0031925', 'Rosette', 'XPO:0140082', 'abnormally necrotic interneuron', 0.4186046511627907, 5.43643956286526, 1.5085486027240909, 'HP:0025461', 'Abnormal cell morphology'),
(465179, 'HP:0031925', 'Rosette', 'XPO:0101498', 'abnormal stage II oocyte', 0.5, 3.6715585125471644, 1.3549093166236559, 'UPHENO:0086172', 'abnormal cell'),
(465180, 'HP:0031925', 'Rosette', 'XPO:0103005', 'abnormal oxygen accumulating cell morphology', 0.6428571428571429, 5.43643956286526, 1.869452862390249, 'HP:0025461', 'Abnormal cell morphology'),
(465181, 'HP:0031925', 'Rosette', 'XPO:0131278', 'abnormally decreased number of keratin accumulating cell', 0.4117647058823529, 3.6715585125471644, 1.229560169755361, 'UPHENO:0086172', 'abnormal cell'),
(465182, 'HP:0031925', 'Rosette', 'XPO:0101468', 'abnormal stage I oocyte', 0.5, 3.6715585125471644, 1.3549093166236559, 'UPHENO:0086172', 'abnormal cell'),
(465183, 'HP:0031925', 'Rosette', 'XPO:0102306', 'abnormal secondary oogonium morphology', 0.6, 5.43643956286526, 1.8060630492092893, 'HP:0025461', 'Abnormal cell morphology'),
(465184, 'HP:0031925', 'Rosette', 'XPO:0102790', 'abnormal blastomere V2.2.2 morphology', 0.43902439024390244, 5.43643956286526, 1.5449043867452603, 'HP:0025461', 'Abnormal cell morphology'),
(465185, 'HP:0031925', 'Rosette', 'XPO:0101967', 'abnormal commissural interneuron morphology', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(465186, 'HP:0031925', 'Rosette', 'XPO:0125115', 'absent paracrine cell', 0.42424242424242425, 3.6715585125471644, 1.2480508339450433, 'UPHENO:0086172', 'abnormal cell'),
(465187, 'HP:0031925', 'Rosette', 'XPO:0103021', 'abnormal wedge region morphology', 0.5161290322580645, 3.6715585125471644, 1.376589242279565, 'UPHENO:0086172', 'abnormal cell'),
(465188, 'HP:0031925', 'Rosette', 'XPO:0101389', 'abnormal wedge region', 0.48148148148148145, 3.6715585125471644, 1.3295816755533123, 'UPHENO:0086172', 'abnormal cell'),
(465189, 'HP:0031925', 'Rosette', 'XPO:0131165', 'abnormally increased number of cementoblast', 0.42424242424242425, 3.6715585125471644, 1.2480508339450433, 'UPHENO:0086172', 'abnormal cell'),
(465190, 'HP:0031925', 'Rosette', 'XPO:0139838', 'abnormally necrotic proepicardium', 0.5142857142857142, 5.43643956286526, 1.6720894724144628, 'HP:0025461', 'Abnormal cell morphology'),
(465191, 'HP:0031925', 'Rosette', 'XPO:0124934', 'absent centrosome', 0.42424242424242425, 3.6715585125471644, 1.2480508339450433, 'UPHENO:0086172', 'abnormal cell'),
(465192, 'HP:0031925', 'Rosette', 'XPO:0128780', 'decreased size of the keratin accumulating cell', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(465193, 'HP:0031925', 'Rosette', 'XPO:0100902', 'abnormal spermatocyte', 0.52, 3.6715585125471644, 1.3817418089225373, 'UPHENO:0086172', 'abnormal cell'),
(465194, 'HP:0031925', 'Rosette', 'XPO:0101463', 'abnormal right-ventral blastomere', 0.48148148148148145, 3.6715585125471644, 1.3295816755533123, 'UPHENO:0086172', 'abnormal cell'),
(465195, 'HP:0031925', 'Rosette', 'XPO:0100570', 'abnormal axon', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(465196, 'HP:0031925', 'Rosette', 'XPO:0115617', 'abnormally posterioralized primordial germ cell', 0.5142857142857142, 5.43643956286526, 1.6720894724144628, 'HP:0025461', 'Abnormal cell morphology'),
(465197, 'HP:0031925', 'Rosette', 'XPO:0140190', 'abnormally necrotic blastomere V2', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(465198, 'HP:0031925', 'Rosette', 'XPO:0102789', 'abnormal female organism morphology', 0.4444444444444444, 2.7446671847279203, 1.104469140402437, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(465199, 'HP:0031925', 'Rosette', 'XPO:0141841', 'abnormality of whole organism mass', 0.41379310344827586, 2.13901709234296, 0.9408031255100615, 'UPHENO:0075696', 'abnormal anatomical entity'),
(465200, 'HP:0031925', 'Rosette', 'XPO:0102872', 'abnormal ciliated non-epidermal cell morphology', 0.6, 5.43643956286526, 1.8060630492092893, 'HP:0025461', 'Abnormal cell morphology'),
(465201, 'HP:0031925', 'Rosette', 'XPO:0125859', 'absent nucleate erythrocyte', 0.42424242424242425, 3.6715585125471644, 1.2480508339450433, 'UPHENO:0086172', 'abnormal cell'),
(465202, 'HP:0031925', 'Rosette', 'XPO:0100702', 'abnormal glial cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(465203, 'HP:0031925', 'Rosette', 'XPO:0102213', 'abnormal immune system morphology', 0.42424242424242425, 2.7446671847279203, 1.0790756508176813, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(465204, 'HP:0031925', 'Rosette', 'XPO:0102028', 'abnormal dorsal animal hemisphere blastomere morphology', 0.46153846153846156, 5.43643956286526, 1.5840220806831131, 'HP:0025461', 'Abnormal cell morphology'),
(465205, 'HP:0031925', 'Rosette', 'XPO:0100691', 'abnormal keratin accumulating cell', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(465206, 'HP:0031925', 'Rosette', 'XPO:0129342', 'decreased size of the centromere', 0.45714285714285713, 3.6715585125471644, 1.2955411026258445, 'UPHENO:0086172', 'abnormal cell'),
(465207, 'HP:0031925', 'Rosette', 'XPO:0102934', 'abnormal subcortical cytoplasm morphology', 0.5161290322580645, 3.6715585125471644, 1.376589242279565, 'UPHENO:0086172', 'abnormal cell'),
(465208, 'HP:0031925', 'Rosette', 'XPO:0101897', 'abnormal sensory epithelial cell morphology', 0.5454545454545454, 5.43643956286526, 1.7220135512398786, 'HP:0025461', 'Abnormal cell morphology'),
(465209, 'HP:0031925', 'Rosette', 'XPO:0127363', 'abnormally localised barrier cell', 0.45161290322580644, 3.6715585125471644, 1.2876813267322194, 'UPHENO:0086172', 'abnormal cell'),
(465210, 'HP:0031925', 'Rosette', 'XPO:0107287', 'abnormal afferent neuron', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(465211, 'HP:0031925', 'Rosette', 'XPO:0100395', 'abnormal blastomere D1.1', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(465212, 'HP:0031925', 'Rosette', 'XPO:0102752', 'abnormal cardiac progenitor cell morphology', 0.4186046511627907, 5.43643956286526, 1.5085486027240909, 'HP:0025461', 'Abnormal cell morphology'),
(465213, 'HP:0031925', 'Rosette', 'XPO:0107353', 'abnormal dorsal side morphology', 0.41379310344827586, 2.7446671847279203, 1.0657036887902793, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(465214, 'HP:0031925', 'Rosette', 'XPO:0101587', 'abnormal hemangioblast', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(465215, 'HP:0031925', 'Rosette', 'XPO:0139733', 'abnormally necrotic vegetal blastomere', 0.4186046511627907, 5.43643956286526, 1.5085486027240909, 'HP:0025461', 'Abnormal cell morphology'),
(465216, 'HP:0031925', 'Rosette', 'XPO:0100733', 'abnormal fibroblast', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(465217, 'HP:0031925', 'Rosette', 'XPO:0133485', 'increased size of the cilium in ciliated non-epidermal cell', 0.41025641025641024, 3.6715585125471644, 1.2273061620492112, 'UPHENO:0086172', 'abnormal cell'),
(465218, 'HP:0031925', 'Rosette', 'XPO:0115510', 'abnormal degeneration of whole organism', 0.46153846153846156, 2.7446671847279203, 1.125508538339192, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(465219, 'HP:0031925', 'Rosette', 'XPO:0131523', 'absent actin filament', 0.4117647058823529, 3.6715585125471644, 1.229560169755361, 'UPHENO:0086172', 'abnormal cell'),
(465220, 'HP:0031925', 'Rosette', 'XPO:0101325', 'abnormal blastomere D2.1.1', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(465221, 'HP:0031925', 'Rosette', 'XPO:0127372', 'abnormally localised polar body', 0.45161290322580644, 3.6715585125471644, 1.2876813267322194, 'UPHENO:0086172', 'abnormal cell'),
(465222, 'HP:0031925', 'Rosette', 'XPO:0124845', 'absent stem cell', 0.42424242424242425, 3.6715585125471644, 1.2480508339450433, 'UPHENO:0086172', 'abnormal cell'),
(465223, 'HP:0031925', 'Rosette', 'XPO:0102599', 'abnormal blastomere V2.1.2 morphology', 0.43902439024390244, 5.43643956286526, 1.5449043867452603, 'HP:0025461', 'Abnormal cell morphology'),
(465224, 'HP:0031925', 'Rosette', 'XPO:0127399', 'abnormally localised melanoblast', 0.45161290322580644, 3.6715585125471644, 1.2876813267322194, 'UPHENO:0086172', 'abnormal cell'),
(465225, 'HP:0031925', 'Rosette', 'XPO:0127288', 'abnormally localised pericyte', 0.45161290322580644, 3.6715585125471644, 1.2876813267322194, 'UPHENO:0086172', 'abnormal cell'),
(465226, 'HP:0031925', 'Rosette', 'XPO:0141277', 'abnormal actin cytoskeleton morphology', 0.5517241379310345, 3.6715585125471644, 1.423266473714053, 'UPHENO:0086172', 'abnormal cell'),
(465227, 'HP:0031925', 'Rosette', 'XPO:0131096', 'abnormally increased number of exocrine cell', 0.42424242424242425, 3.6715585125471644, 1.2480508339450433, 'UPHENO:0086172', 'abnormal cell'),
(465228, 'HP:0031925', 'Rosette', 'XPO:0130899', 'increased size of the microtubule', 0.45714285714285713, 3.6715585125471644, 1.2955411026258445, 'UPHENO:0086172', 'abnormal cell'),
(465229, 'HP:0031925', 'Rosette', 'XPO:0102423', 'abnormal multiciliated cell precursor morphology', 0.6428571428571429, 5.43643956286526, 1.869452862390249, 'HP:0025461', 'Abnormal cell morphology'),
(465230, 'HP:0031925', 'Rosette', 'XPO:0141195', 'abnormally necrotic somatic stem cell', 0.5142857142857142, 5.43643956286526, 1.6720894724144628, 'HP:0025461', 'Abnormal cell morphology'),
(465231, 'HP:0031925', 'Rosette', 'XPO:0102270', 'abnormal polar body morphology', 0.46153846153846156, 5.43643956286526, 1.5840220806831131, 'HP:0025461', 'Abnormal cell morphology'),
(465232, 'HP:0031925', 'Rosette', 'XPO:0141007', 'abnormally necrotic electrically active cell', 0.5625, 5.43643956286526, 1.748713027947041, 'HP:0025461', 'Abnormal cell morphology'),
(465233, 'HP:0031925', 'Rosette', 'XPO:0130949', 'increased size of the wedge region', 0.43243243243243246, 3.6715585125471644, 1.2600400701560144, 'UPHENO:0086172', 'abnormal cell'),
(465234, 'HP:0031925', 'Rosette', 'XPO:0128037', 'decreased size of the anatomical space', 0.41379310344827586, 2.7446671847279203, 1.0657036887902793, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(465235, 'HP:0031925', 'Rosette', 'XPO:0101132', 'abnormal apoptotic cell', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(465236, 'HP:0031925', 'Rosette', 'XPO:0102625', 'abnormal ligament cell morphology', 0.4864864864864865, 5.43643956286526, 1.626270082715184, 'HP:0025461', 'Abnormal cell morphology'),
(465237, 'HP:0031925', 'Rosette', 'XPO:0127979', 'abnormally localised absorptive cell', 0.45161290322580644, 3.6715585125471644, 1.2876813267322194, 'UPHENO:0086172', 'abnormal cell'),
(465238, 'HP:0031925', 'Rosette', 'XPO:0127513', 'abnormally localised nucleate erythrocyte', 0.45161290322580644, 3.6715585125471644, 1.2876813267322194, 'UPHENO:0086172', 'abnormal cell'),
(465239, 'HP:0031925', 'Rosette', 'XPO:0101326', 'abnormal cementoblast', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(465240, 'HP:0031925', 'Rosette', 'XPO:0100626', 'abnormal primordial germ cell', 0.52, 3.6715585125471644, 1.3817418089225373, 'UPHENO:0086172', 'abnormal cell'),
(465241, 'HP:0031925', 'Rosette', 'XPO:0100520', 'abnormal blastomere D1.2', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(465242, 'HP:0031925', 'Rosette', 'XPO:0140896', 'abnormally necrotic dorsolateral ascending neuron', 0.42857142857142855, 5.43643956286526, 1.526401870347189, 'HP:0025461', 'Abnormal cell morphology'),
(465243, 'HP:0031925', 'Rosette', 'XPO:0125976', 'absent centriole', 0.4117647058823529, 3.6715585125471644, 1.229560169755361, 'UPHENO:0086172', 'abnormal cell'),
(465244, 'HP:0031925', 'Rosette', 'XPO:0126630', 'abnormally localised early embryonic cell', 0.4375, 3.6715585125471644, 1.2674016132384338, 'UPHENO:0086172', 'abnormal cell'),
(465245, 'HP:0031925', 'Rosette', 'XPO:0140010', 'abnormally necrotic zygote', 0.5625, 5.43643956286526, 1.748713027947041, 'HP:0025461', 'Abnormal cell morphology'),
(465246, 'HP:0031925', 'Rosette', 'XPO:0128903', 'decreased size of the multiciliated cell', 0.4186046511627907, 5.43643956286526, 1.5085486027240909, 'HP:0025461', 'Abnormal cell morphology'),
(465247, 'HP:0031925', 'Rosette', 'XPO:0102910', 'abnormal pigment cell morphology', 0.43902439024390244, 5.43643956286526, 1.5449043867452603, 'HP:0025461', 'Abnormal cell morphology'),
(465248, 'HP:0031925', 'Rosette', 'XPO:0140663', 'abnormally necrotic right-ventral blastomere', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(465249, 'HP:0031925', 'Rosette', 'XPO:0102929', 'abnormal barrier cell morphology', 0.6428571428571429, 5.43643956286526, 1.869452862390249, 'HP:0025461', 'Abnormal cell morphology'),
(465250, 'HP:0031925', 'Rosette', 'XPO:0133471', 'abnormally decreased number of cilium in the ciliated cell', 0.4375, 3.6715585125471644, 1.2674016132384338, 'UPHENO:0086172', 'abnormal cell'),
(465251, 'HP:0031925', 'Rosette', 'XPO:0141511', 'abnormally localised nucleus in myoblast', 0.4117647058823529, 3.6715585125471644, 1.229560169755361, 'UPHENO:0086172', 'abnormal cell'),
(465252, 'HP:0031925', 'Rosette', 'XPO:0103126', 'abnormal blastomere D1.2.1 morphology', 0.43902439024390244, 5.43643956286526, 1.5449043867452603, 'HP:0025461', 'Abnormal cell morphology'),
(465253, 'HP:0031925', 'Rosette', 'XPO:0102286', 'abnormal blastomere V2.1 morphology', 0.43902439024390244, 5.43643956286526, 1.5449043867452603, 'HP:0025461', 'Abnormal cell morphology'),
(465254, 'HP:0031925', 'Rosette', 'XPO:0130376', 'increased size of the apoptotic cell', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(465255, 'HP:0031925', 'Rosette', 'XPO:0140358', 'abnormally necrotic non-ciliated epithelial cell', 0.47368421052631576, 5.43643956286526, 1.6047291305419304, 'HP:0025461', 'Abnormal cell morphology'),
(465256, 'HP:0031925', 'Rosette', 'XPO:0102474', 'abnormal left-dorsal blastomere morphology', 0.5294117647058824, 5.43643956286526, 1.696500828969256, 'HP:0025461', 'Abnormal cell morphology'),
(465257, 'HP:0031925', 'Rosette', 'XPO:0139734', 'abnormally necrotic blastomere', 0.4864864864864865, 5.43643956286526, 1.626270082715184, 'HP:0025461', 'Abnormal cell morphology'),
(465258, 'HP:0031925', 'Rosette', 'XPO:0130739', 'increased size of the mitochondrial cloud', 0.43243243243243246, 3.6715585125471644, 1.2600400701560144, 'UPHENO:0086172', 'abnormal cell'),
(465259, 'HP:0031925', 'Rosette', 'XPO:0103104', 'abnormal zygote cortex morphology', 0.5333333333333333, 3.6715585125471644, 1.399344325041251, 'UPHENO:0086172', 'abnormal cell'),
(465260, 'HP:0031925', 'Rosette', 'XPO:0130215', 'increased size of the perivitelline space', 0.43243243243243246, 3.6715585125471644, 1.2600400701560144, 'UPHENO:0086172', 'abnormal cell'),
(465261, 'HP:0031925', 'Rosette', 'XPO:0102592', 'abnormal postmigratory neural crest cell morphology', 0.43902439024390244, 5.43643956286526, 1.5449043867452603, 'HP:0025461', 'Abnormal cell morphology'),
(465262, 'HP:0031925', 'Rosette', 'XPO:0142050', 'increased size of the desmosome', 0.45714285714285713, 3.6715585125471644, 1.2955411026258445, 'UPHENO:0086172', 'abnormal cell'),
(465263, 'HP:0031925', 'Rosette', 'XPO:0101636', 'abnormal cell morphology', 0.6923076923076923, 5.43643956286526, 1.9400229194876766, 'HP:0025461', 'Abnormal cell morphology'),
(465264, 'HP:0031925', 'Rosette', 'XPO:0101807', 'abnormal migrating neuroblast morphology', 0.5142857142857142, 5.43643956286526, 1.6720894724144628, 'HP:0025461', 'Abnormal cell morphology'),
(465265, 'HP:0031925', 'Rosette', 'XPO:0141299', 'abnormal actin filament morphology', 0.5333333333333333, 3.6715585125471644, 1.399344325041251, 'UPHENO:0086172', 'abnormal cell'),
(465266, 'HP:0031925', 'Rosette', 'XPO:0101927', 'abnormal extracellular matrix morphology', 0.42857142857142855, 2.7446671847279203, 1.0845671654222093, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(465267, 'HP:0031925', 'Rosette', 'XPO:0129087', 'decreased size of the ciliated non-epidermal cell', 0.4186046511627907, 5.43643956286526, 1.5085486027240909, 'HP:0025461', 'Abnormal cell morphology'),
(465268, 'HP:0031925', 'Rosette', 'XPO:0130389', 'increased size of the barrier cell', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(465269, 'HP:0031925', 'Rosette', 'XPO:0100025', 'abnormal oocyte', 0.52, 3.6715585125471644, 1.3817418089225373, 'UPHENO:0086172', 'abnormal cell'),
(465270, 'HP:0031925', 'Rosette', 'XPO:0129620', 'increased size of the electrically active cell', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(465271, 'HP:0031925', 'Rosette', 'XPO:0131307', 'abnormally decreased number of mitotic cell', 0.4117647058823529, 3.6715585125471644, 1.229560169755361, 'UPHENO:0086172', 'abnormal cell'),
(465272, 'HP:0031925', 'Rosette', 'XPO:0102519', 'abnormal right-dorsal blastomere morphology', 0.5294117647058824, 5.43643956286526, 1.696500828969256, 'HP:0025461', 'Abnormal cell morphology'),
(465273, 'HP:0031925', 'Rosette', 'XPO:0127643', 'abnormally localised somatic stem cell', 0.42424242424242425, 3.6715585125471644, 1.2480508339450433, 'UPHENO:0086172', 'abnormal cell'),
(465274, 'HP:0031925', 'Rosette', 'XPO:0100481', 'abnormal anatomical line', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(465275, 'HP:0031925', 'Rosette', 'XPO:0128637', 'decreased size of the secondary spermatogonium', 0.4186046511627907, 5.43643956286526, 1.5085486027240909, 'HP:0025461', 'Abnormal cell morphology'),
(465276, 'HP:0031925', 'Rosette', 'XPO:0128382', 'decreased size of the myoblast', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(465277, 'HP:0031925', 'Rosette', 'XPO:0102957', 'abnormal blastomere D2.1.1 morphology', 0.43902439024390244, 5.43643956286526, 1.5449043867452603, 'HP:0025461', 'Abnormal cell morphology'),
(465278, 'HP:0031925', 'Rosette', 'XPO:0101192', 'abnormal blastomere D2.1', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(465279, 'HP:0031925', 'Rosette', 'XPO:0131328', 'abnormally decreased number of paracrine cell', 0.4117647058823529, 3.6715585125471644, 1.229560169755361, 'UPHENO:0086172', 'abnormal cell'),
(465280, 'HP:0031925', 'Rosette', 'XPO:0101667', 'abnormal ventral animal hemisphere blastomere morphology', 0.46153846153846156, 5.43643956286526, 1.5840220806831131, 'HP:0025461', 'Abnormal cell morphology'),
(465281, 'HP:0031925', 'Rosette', 'XPO:0142023', 'absent desmosome', 0.42424242424242425, 3.6715585125471644, 1.2480508339450433, 'UPHENO:0086172', 'abnormal cell'),
(465282, 'HP:0031925', 'Rosette', 'XPO:0140098', 'abnormally necrotic secondary spermatogonium', 0.5142857142857142, 5.43643956286526, 1.6720894724144628, 'HP:0025461', 'Abnormal cell morphology'),
(465283, 'HP:0031925', 'Rosette', 'XPO:0141065', 'abnormally necrotic paracrine cell', 0.5625, 5.43643956286526, 1.748713027947041, 'HP:0025461', 'Abnormal cell morphology'),
(465284, 'HP:0031925', 'Rosette', 'XPO:0126671', 'abnormally localised zygote', 0.45161290322580644, 3.6715585125471644, 1.2876813267322194, 'UPHENO:0086172', 'abnormal cell'),
(465285, 'HP:0031925', 'Rosette', 'XPO:0131131', 'abnormally increased number of absorptive cell', 0.42424242424242425, 3.6715585125471644, 1.2480508339450433, 'UPHENO:0086172', 'abnormal cell'),
(465286, 'HP:0031925', 'Rosette', 'XPO:0127683', 'abnormally localised centromere', 0.4375, 3.6715585125471644, 1.2674016132384338, 'UPHENO:0086172', 'abnormal cell'),
(465287, 'HP:0031925', 'Rosette', 'XPO:0100172', 'abnormal stem cell', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(465288, 'HP:0031925', 'Rosette', 'XPO:0102764', 'abnormal apoptotic cell morphology', 0.6428571428571429, 5.43643956286526, 1.869452862390249, 'HP:0025461', 'Abnormal cell morphology'),
(465289, 'HP:0031925', 'Rosette', 'XPO:0107411', 'abnormal embryonic thrombocyte morphology', 0.4090909090909091, 5.43643956286526, 1.491307481034791, 'HP:0025461', 'Abnormal cell morphology'),
(465290, 'HP:0031925', 'Rosette', 'XPO:0103117', 'abnormal descending interneuron morphology', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(465291, 'HP:0031925', 'Rosette', 'XPO:0100784', 'abnormal left blastomere', 0.48148148148148145, 3.6715585125471644, 1.3295816755533123, 'UPHENO:0086172', 'abnormal cell'),
(465292, 'HP:0031925', 'Rosette', 'XPO:0128071', 'decreased size of the cell part', 0.5, 3.6715585125471644, 1.3549093166236559, 'UPHENO:0086172', 'abnormal cell'),
(465293, 'HP:0031925', 'Rosette', 'XPO:0126388', 'abnormally localised oocyte', 0.42424242424242425, 3.6715585125471644, 1.2480508339450433, 'UPHENO:0086172', 'abnormal cell'),
(465294, 'HP:0031925', 'Rosette', 'XPO:0102641', 'abnormal blastomere D1.1.1 morphology', 0.43902439024390244, 5.43643956286526, 1.5449043867452603, 'HP:0025461', 'Abnormal cell morphology'),
(465295, 'HP:0031925', 'Rosette', 'XPO:0125530', 'absent chondroblast', 0.42424242424242425, 3.6715585125471644, 1.2480508339450433, 'UPHENO:0086172', 'abnormal cell'),
(465296, 'HP:0031925', 'Rosette', 'XPO:0128874', 'decreased size of the ciliary axoneme', 0.43243243243243246, 3.6715585125471644, 1.2600400701560144, 'UPHENO:0086172', 'abnormal cell'),
(465297, 'HP:0031925', 'Rosette', 'XPO:0126600', 'abnormally localised progenitor cell', 0.45161290322580644, 3.6715585125471644, 1.2876813267322194, 'UPHENO:0086172', 'abnormal cell'),
(465298, 'HP:0031925', 'Rosette', 'XPO:0141510', 'abnormal epithelial cell morphology in the foregut endoderm', 0.42857142857142855, 5.43643956286526, 1.526401870347189, 'HP:0025461', 'Abnormal cell morphology'),
(465299, 'HP:0031925', 'Rosette', 'XPO:0103095', 'abnormal right-ventral blastomere morphology', 0.5294117647058824, 5.43643956286526, 1.696500828969256, 'HP:0025461', 'Abnormal cell morphology'),
(465300, 'HP:0031925', 'Rosette', 'XPO:0128006', 'decreased size of the cell', 0.4864864864864865, 5.43643956286526, 1.626270082715184, 'HP:0025461', 'Abnormal cell morphology'),
(465301, 'HP:0031925', 'Rosette', 'XPO:0128988', 'decreased size of the migrating myoblast', 0.4186046511627907, 5.43643956286526, 1.5085486027240909, 'HP:0025461', 'Abnormal cell morphology'),
(465302, 'HP:0031925', 'Rosette', 'XPO:0100429', 'abnormal spermatid', 0.52, 3.6715585125471644, 1.3817418089225373, 'UPHENO:0086172', 'abnormal cell'),
(465303, 'HP:0031925', 'Rosette', 'XPO:0100852', 'abnormal interdigital region', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(465304, 'HP:0031925', 'Rosette', 'XPO:0100175', 'abnormal migrating neuroblast', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(465305, 'HP:0031925', 'Rosette', 'XPO:0130988', 'abnormally increased number of pericyte', 0.42424242424242425, 3.6715585125471644, 1.2480508339450433, 'UPHENO:0086172', 'abnormal cell'),
(465306, 'HP:0031925', 'Rosette', 'XPO:0131297', 'abnormally decreased number of melanoblast', 0.4117647058823529, 3.6715585125471644, 1.229560169755361, 'UPHENO:0086172', 'abnormal cell'),
(465307, 'HP:0031925', 'Rosette', 'XPO:0102706', 'abnormal germinal vesicle morphology', 0.48484848484848486, 3.6715585125471644, 1.3342224633999569, 'UPHENO:0086172', 'abnormal cell'),
(465308, 'HP:0031925', 'Rosette', 'XPO:0107347', 'abnormal anterior-posterior axis morphology', 0.4444444444444444, 2.7446671847279203, 1.104469140402437, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(465309, 'HP:0031925', 'Rosette', 'XPO:0115758', 'abnormally decreased mobility of melanoblast', 0.5185185185185185, 3.6715585125471644, 1.3797721118286204, 'UPHENO:0086172', 'abnormal cell'),
(465310, 'HP:0031925', 'Rosette', 'XPO:0102027', 'abnormal blastomere D1.1 morphology', 0.43902439024390244, 5.43643956286526, 1.5449043867452603, 'HP:0025461', 'Abnormal cell morphology'),
(465311, 'HP:0031925', 'Rosette', 'XPO:0129709', 'increased size of the early embryonic cell', 0.42857142857142855, 5.43643956286526, 1.526401870347189, 'HP:0025461', 'Abnormal cell morphology'),
(465312, 'HP:0031925', 'Rosette', 'XPO:0101480', 'abnormal stage V oocyte', 0.5, 3.6715585125471644, 1.3549093166236559, 'UPHENO:0086172', 'abnormal cell'),
(465313, 'HP:0031925', 'Rosette', 'XPO:0141135', 'abnormally necrotic spermatid', 0.5142857142857142, 5.43643956286526, 1.6720894724144628, 'HP:0025461', 'Abnormal cell morphology'),
(465314, 'HP:0031925', 'Rosette', 'XPO:0102205', 'abnormal extraembryonic structure morphology', 0.4444444444444444, 2.7446671847279203, 1.104469140402437, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(465315, 'HP:0031925', 'Rosette', 'XPO:0141049', 'abnormally necrotic perivitelline space', 0.45714285714285713, 3.6715585125471644, 1.2955411026258445, 'UPHENO:0086172', 'abnormal cell'),
(465316, 'HP:0031925', 'Rosette', 'XPO:0102588', 'abnormal centrosome morphology', 0.5517241379310345, 3.6715585125471644, 1.423266473714053, 'UPHENO:0086172', 'abnormal cell'),
(465317, 'HP:0031925', 'Rosette', 'XPO:0101264', 'abnormal mitotic spindle', 0.52, 3.6715585125471644, 1.3817418089225373, 'UPHENO:0086172', 'abnormal cell'),
(465318, 'HP:0031925', 'Rosette', 'XPO:0131153', 'abnormally increased number of electrically active cell', 0.42424242424242425, 3.6715585125471644, 1.2480508339450433, 'UPHENO:0086172', 'abnormal cell'),
(465319, 'HP:0031925', 'Rosette', 'XPO:0127391', 'abnormally localised lampbrush chromosome', 0.4375, 3.6715585125471644, 1.2674016132384338, 'UPHENO:0086172', 'abnormal cell'),
(465320, 'HP:0031925', 'Rosette', 'XPO:0131314', 'abnormally decreased number of exocrine cell', 0.4117647058823529, 3.6715585125471644, 1.229560169755361, 'UPHENO:0086172', 'abnormal cell'),
(465321, 'HP:0031925', 'Rosette', 'XPO:0102333', 'abnormal microglial cell morphology', 0.4864864864864865, 5.43643956286526, 1.626270082715184, 'HP:0025461', 'Abnormal cell morphology'),
(465322, 'HP:0031925', 'Rosette', 'XPO:0107312', 'abnormal filopodium', 0.52, 3.6715585125471644, 1.3817418089225373, 'UPHENO:0086172', 'abnormal cell'),
(465323, 'HP:0031925', 'Rosette', 'XPO:0127520', 'abnormally localised gastrula cell', 0.4117647058823529, 3.6715585125471644, 1.229560169755361, 'UPHENO:0086172', 'abnormal cell'),
(465324, 'HP:0031925', 'Rosette', 'XPO:0101110', 'abnormal cell-free extract', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(465325, 'HP:0031925', 'Rosette', 'XPO:0102597', 'abnormal blastomere V2.2 morphology', 0.43902439024390244, 5.43643956286526, 1.5449043867452603, 'HP:0025461', 'Abnormal cell morphology'),
(465326, 'HP:0031925', 'Rosette', 'XPO:0128760', 'decreased size of the oocyte cortex', 0.43243243243243246, 3.6715585125471644, 1.2600400701560144, 'UPHENO:0086172', 'abnormal cell'),
(465327, 'HP:0031925', 'Rosette', 'XPO:0107356', 'abnormal right side morphology', 0.41379310344827586, 2.7446671847279203, 1.0657036887902793, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(465328, 'HP:0031925', 'Rosette', 'XPO:0130867', 'increased size of the barrier epithelial cell', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(465329, 'HP:0031925', 'Rosette', 'XPO:0126082', 'absent perivitelline space', 0.4117647058823529, 3.6715585125471644, 1.229560169755361, 'UPHENO:0086172', 'abnormal cell'),
(465330, 'HP:0031925', 'Rosette', 'XPO:0133436', 'abnormal cilium morphology in the multiciliated cell', 0.5, 3.6715585125471644, 1.3549093166236559, 'UPHENO:0086172', 'abnormal cell'),
(465331, 'HP:0031925', 'Rosette', 'XPO:0128684', 'decreased size of the basal body', 0.45714285714285713, 3.6715585125471644, 1.2955411026258445, 'UPHENO:0086172', 'abnormal cell'),
(465332, 'HP:0031925', 'Rosette', 'XPO:0100035', 'abnormal ventral animal hemisphere blastomere', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(465333, 'HP:0031925', 'Rosette', 'XPO:0131180', 'abnormally decreased number of cell', 0.4375, 3.6715585125471644, 1.2674016132384338, 'UPHENO:0086172', 'abnormal cell'),
(465334, 'HP:0031925', 'Rosette', 'XPO:0141288', 'abnormal astral microtubule morphology', 0.48484848484848486, 3.6715585125471644, 1.3342224633999569, 'UPHENO:0086172', 'abnormal cell'),
(465335, 'HP:0031925', 'Rosette', 'XPO:0131354', 'abnormally decreased number of multiciliated cell precursor', 0.4117647058823529, 3.6715585125471644, 1.229560169755361, 'UPHENO:0086172', 'abnormal cell'),
(465336, 'HP:0031925', 'Rosette', 'XPO:0131675', 'abnormal spindle microtubule', 0.5, 3.6715585125471644, 1.3549093166236559, 'UPHENO:0086172', 'abnormal cell'),
(465337, 'HP:0031925', 'Rosette', 'XPO:0131669', 'abnormal Roux spot', 0.48148148148148145, 3.6715585125471644, 1.3295816755533123, 'UPHENO:0086172', 'abnormal cell'),
(465338, 'HP:0031925', 'Rosette', 'XPO:0141555', 'abnormal neuron morphology in the regenerating tail', 0.43902439024390244, 5.43643956286526, 1.5449043867452603, 'HP:0025461', 'Abnormal cell morphology'),
(465339, 'HP:0031925', 'Rosette', 'XPO:0125577', 'absent cilium', 0.4117647058823529, 3.6715585125471644, 1.229560169755361, 'UPHENO:0086172', 'abnormal cell'),
(465340, 'HP:0031925', 'Rosette', 'XPO:0141334', 'increased pigmentation in the whole organism', 0.42857142857142855, 2.7446671847279203, 1.0845671654222093, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(465341, 'HP:0031925', 'Rosette', 'XPO:0101366', 'abnormal morula cell', 0.5, 3.6715585125471644, 1.3549093166236559, 'UPHENO:0086172', 'abnormal cell'),
(465342, 'HP:0031925', 'Rosette', 'XPO:0102869', 'abnormal mucus secreting cell morphology', 0.6428571428571429, 5.43643956286526, 1.869452862390249, 'HP:0025461', 'Abnormal cell morphology'),
(465343, 'HP:0031925', 'Rosette', 'XPO:0100654', 'abnormal blastomere V2.1', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(465344, 'HP:0031925', 'Rosette', 'XPO:0130163', 'increased size of the basal body', 0.45714285714285713, 3.6715585125471644, 1.2955411026258445, 'UPHENO:0086172', 'abnormal cell'),
(465345, 'HP:0031925', 'Rosette', 'XPO:0141076', 'abnormally necrotic secondary myofiber', 0.4090909090909091, 5.43643956286526, 1.491307481034791, 'HP:0025461', 'Abnormal cell morphology'),
(465346, 'HP:0031925', 'Rosette', 'XPO:0140104', 'abnormally necrotic circulating cell', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(465347, 'HP:0031925', 'Rosette', 'XPO:0128961', 'decreased size of the Merkel cell', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(465348, 'HP:0031925', 'Rosette', 'XPO:0101490', 'abnormal ectodermal cell', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(465349, 'HP:0031925', 'Rosette', 'XPO:0101921', 'abnormal chondroblast morphology', 0.6428571428571429, 5.43643956286526, 1.869452862390249, 'HP:0025461', 'Abnormal cell morphology'),
(465350, 'HP:0031925', 'Rosette', 'XPO:0128898', 'decreased size of the apoptotic cell', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(465351, 'HP:0031925', 'Rosette', 'XPO:0102819', 'abnormal dorsolateral commissural neuron morphology', 0.4864864864864865, 5.43643956286526, 1.626270082715184, 'HP:0025461', 'Abnormal cell morphology'),
(465352, 'HP:0031925', 'Rosette', 'XPO:0101166', 'abnormal premigratory neural crest cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(465353, 'HP:0031925', 'Rosette', 'XPO:0103756', 'increased size of the germ cell', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(465354, 'HP:0031925', 'Rosette', 'XPO:0124807', 'absent cell part', 0.45161290322580644, 3.6715585125471644, 1.2876813267322194, 'UPHENO:0086172', 'abnormal cell'),
(465355, 'HP:0031925', 'Rosette', 'XPO:0130212', 'increased size of the spermatocyte', 0.4186046511627907, 5.43643956286526, 1.5085486027240909, 'HP:0025461', 'Abnormal cell morphology'),
(465356, 'HP:0031925', 'Rosette', 'XPO:0140919', 'abnormally necrotic cementoblast', 0.5625, 5.43643956286526, 1.748713027947041, 'HP:0025461', 'Abnormal cell morphology'),
(465357, 'HP:0031925', 'Rosette', 'XPO:0127703', 'abnormally localised morula cell', 0.4117647058823529, 3.6715585125471644, 1.229560169755361, 'UPHENO:0086172', 'abnormal cell'),
(465358, 'HP:0031925', 'Rosette', 'XPO:0140803', 'abnormally necrotic pericyte', 0.5625, 5.43643956286526, 1.748713027947041, 'HP:0025461', 'Abnormal cell morphology'),
(465359, 'HP:0031925', 'Rosette', 'XPO:0129551', 'increased size of the cell part', 0.5, 3.6715585125471644, 1.3549093166236559, 'UPHENO:0086172', 'abnormal cell'),
(465360, 'HP:0031925', 'Rosette', 'XPO:0131129', 'abnormally increased number of chondroblast', 0.42424242424242425, 3.6715585125471644, 1.2480508339450433, 'UPHENO:0086172', 'abnormal cell'),
(465361, 'HP:0031925', 'Rosette', 'XPO:0101642', 'abnormal multicellular anatomical structure morphology', 0.46153846153846156, 2.7446671847279203, 1.125508538339192, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(465362, 'HP:0031925', 'Rosette', 'XPO:0100437', 'abnormal proepicardium', 0.52, 3.6715585125471644, 1.3817418089225373, 'UPHENO:0086172', 'abnormal cell'),
(465363, 'HP:0031925', 'Rosette', 'XPO:0131204', 'abnormally decreased number of pericyte', 0.4117647058823529, 3.6715585125471644, 1.229560169755361, 'UPHENO:0086172', 'abnormal cell'),
(465364, 'HP:0031925', 'Rosette', 'XPO:0102189', 'abnormal prime meridian morphology', 0.41379310344827586, 2.7446671847279203, 1.0657036887902793, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(465365, 'HP:0031925', 'Rosette', 'XPO:0101350', 'abnormal blastomere D2.1.2', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(465366, 'HP:0031925', 'Rosette', 'XPO:0101964', 'abnormal germinal granule morphology', 0.45714285714285713, 3.6715585125471644, 1.2955411026258445, 'UPHENO:0086172', 'abnormal cell'),
(465367, 'HP:0031925', 'Rosette', 'XPO:0101187', 'abnormal dorsolateral commissural neuron', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(465368, 'HP:0031925', 'Rosette', 'XPO:0101378', 'abnormal blastomere D1', 0.48148148148148145, 3.6715585125471644, 1.3295816755533123, 'UPHENO:0086172', 'abnormal cell'),
(465369, 'HP:0031925', 'Rosette', 'XPO:0125454', 'absent myoblast', 0.42424242424242425, 3.6715585125471644, 1.2480508339450433, 'UPHENO:0086172', 'abnormal cell'),
(465370, 'HP:0031925', 'Rosette', 'XPO:0102741', 'abnormal egg cell-free extract morphology', 0.4444444444444444, 2.7446671847279203, 1.104469140402437, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(465371, 'HP:0031925', 'Rosette', 'XPO:0130615', 'increased size of the kinetochore', 0.45714285714285713, 3.6715585125471644, 1.2955411026258445, 'UPHENO:0086172', 'abnormal cell'),
(465372, 'HP:0031925', 'Rosette', 'XPO:0141123', 'abnormally necrotic microglial cell', 0.42857142857142855, 5.43643956286526, 1.526401870347189, 'HP:0025461', 'Abnormal cell morphology'),
(465373, 'HP:0031925', 'Rosette', 'XPO:0102977', 'abnormal ascending interneuron morphology', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(465374, 'HP:0031925', 'Rosette', 'XPO:0101917', 'abnormal progenitor cell morphology', 0.6428571428571429, 5.43643956286526, 1.869452862390249, 'HP:0025461', 'Abnormal cell morphology'),
(465375, 'HP:0031925', 'Rosette', 'XPO:0140938', 'abnormally necrotic secretory epithelial cell', 0.47368421052631576, 5.43643956286526, 1.6047291305419304, 'HP:0025461', 'Abnormal cell morphology'),
(465376, 'HP:0031925', 'Rosette', 'XPO:0131089', 'abnormally increased number of mitotic cell', 0.42424242424242425, 3.6715585125471644, 1.2480508339450433, 'UPHENO:0086172', 'abnormal cell'),
(465377, 'HP:0031925', 'Rosette', 'XPO:0140505', 'abnormally necrotic stromal cell', 0.47368421052631576, 5.43643956286526, 1.6047291305419304, 'HP:0025461', 'Abnormal cell morphology'),
(465378, 'HP:0031925', 'Rosette', 'XPO:0142064', 'abnormal desmosome morphology', 0.5517241379310345, 3.6715585125471644, 1.423266473714053, 'UPHENO:0086172', 'abnormal cell'),
(465379, 'HP:0031925', 'Rosette', 'XPO:0101450', 'abnormal myeloid cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(465380, 'HP:0031925', 'Rosette', 'XPO:0128229', 'decreased size of the early embryonic cell', 0.42857142857142855, 5.43643956286526, 1.526401870347189, 'HP:0025461', 'Abnormal cell morphology'),
(465381, 'HP:0031925', 'Rosette', 'XPO:0102323', 'abnormal keratin accumulating cell morphology', 0.6428571428571429, 5.43643956286526, 1.869452862390249, 'HP:0025461', 'Abnormal cell morphology'),
(465382, 'HP:0031925', 'Rosette', 'XPO:0140567', 'abnormally necrotic postero-ventral region', 0.42857142857142855, 2.7446671847279203, 1.0845671654222093, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(465383, 'HP:0031925', 'Rosette', 'XPO:0101327', 'abnormal blastomere V1.2.1', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(465384, 'HP:0031925', 'Rosette', 'XPO:0100551', 'abnormal oocyte cortex', 0.48148148148148145, 3.6715585125471644, 1.3295816755533123, 'UPHENO:0086172', 'abnormal cell'),
(465385, 'HP:0031925', 'Rosette', 'XPO:0115615', 'abnormally posteriorly mislocalised primordial germ cell', 0.4117647058823529, 3.6715585125471644, 1.229560169755361, 'UPHENO:0086172', 'abnormal cell'),
(465386, 'HP:0031925', 'Rosette', 'XPO:0140670', 'abnormally necrotic afferent neuron', 0.4186046511627907, 5.43643956286526, 1.5085486027240909, 'HP:0025461', 'Abnormal cell morphology'),
(465387, 'HP:0031925', 'Rosette', 'XPO:0103129', 'abnormal ciliary axoneme morphology', 0.5161290322580645, 3.6715585125471644, 1.376589242279565, 'UPHENO:0086172', 'abnormal cell'),
(465388, 'HP:0031925', 'Rosette', 'XPO:0141286', 'abnormal neuron projection morphology', 0.43243243243243246, 3.6715585125471644, 1.2600400701560144, 'UPHENO:0086172', 'abnormal cell'),
(465389, 'HP:0031925', 'Rosette', 'XPO:0102416', 'abnormal left blastomere morphology', 0.5294117647058824, 5.43643956286526, 1.696500828969256, 'HP:0025461', 'Abnormal cell morphology'),
(465390, 'HP:0031925', 'Rosette', 'XPO:0128836', 'decreased size of the acid secreting cell', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(465391, 'HP:0031925', 'Rosette', 'XPO:0140423', 'abnormally necrotic left blastomere', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(465392, 'HP:0031925', 'Rosette', 'XPO:0140167', 'abnormally necrotic medial region', 0.41379310344827586, 2.7446671847279203, 1.0657036887902793, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(465393, 'HP:0031925', 'Rosette', 'XPO:0102531', 'abnormal secondary spermatogonium morphology', 0.6, 5.43643956286526, 1.8060630492092893, 'HP:0025461', 'Abnormal cell morphology'),
(465394, 'HP:0031925', 'Rosette', 'XPO:0126725', 'abnormally localised epithelial cell', 0.4117647058823529, 3.6715585125471644, 1.229560169755361, 'UPHENO:0086172', 'abnormal cell'),
(465395, 'HP:0031925', 'Rosette', 'XPO:0124716', 'absent cell', 0.45161290322580644, 3.6715585125471644, 1.2876813267322194, 'UPHENO:0086172', 'abnormal cell'),
(465396, 'HP:0031925', 'Rosette', 'XPO:0101804', 'abnormal stem cell morphology', 0.6428571428571429, 5.43643956286526, 1.869452862390249, 'HP:0025461', 'Abnormal cell morphology'),
(465397, 'HP:0031925', 'Rosette', 'XPO:0100732', 'abnormal tendon fibroblast', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(465398, 'HP:0031925', 'Rosette', 'XPO:0125785', 'absent mitotic spindle', 0.42424242424242425, 3.6715585125471644, 1.2480508339450433, 'UPHENO:0086172', 'abnormal cell'),
(465399, 'HP:0031925', 'Rosette', 'XPO:0130043', 'increased size of the primordial germ cell', 0.4186046511627907, 5.43643956286526, 1.5085486027240909, 'HP:0025461', 'Abnormal cell morphology'),
(465400, 'HP:0031925', 'Rosette', 'XPO:0102055', 'abnormal process morphology', 0.46153846153846156, 2.7446671847279203, 1.125508538339192, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(465401, 'HP:0031925', 'Rosette', 'XPO:0107355', 'abnormal left side morphology', 0.41379310344827586, 2.7446671847279203, 1.0657036887902793, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(465402, 'HP:0031925', 'Rosette', 'XPO:0140164', 'abnormally necrotic animal blastomere', 0.4186046511627907, 5.43643956286526, 1.5085486027240909, 'HP:0025461', 'Abnormal cell morphology'),
(465403, 'HP:0031925', 'Rosette', 'XPO:0139759', 'abnormally necrotic germ cell', 0.5625, 5.43643956286526, 1.748713027947041, 'HP:0025461', 'Abnormal cell morphology'),
(465404, 'HP:0031925', 'Rosette', 'XPO:0127631', 'abnormally localised centriole', 0.42424242424242425, 3.6715585125471644, 1.2480508339450433, 'UPHENO:0086172', 'abnormal cell'),
(465405, 'HP:0031925', 'Rosette', 'XPO:0101071', 'abnormal endoplasmic reticulum', 0.52, 3.6715585125471644, 1.3817418089225373, 'UPHENO:0086172', 'abnormal cell'),
(465406, 'HP:0031925', 'Rosette', 'XPO:0100724', 'abnormal kinetochore', 0.52, 3.6715585125471644, 1.3817418089225373, 'UPHENO:0086172', 'abnormal cell'),
(465407, 'HP:0031925', 'Rosette', 'XPO:0101283', 'abnormal left-ventral blastomere', 0.48148148148148145, 3.6715585125471644, 1.3295816755533123, 'UPHENO:0086172', 'abnormal cell'),
(465408, 'HP:0031925', 'Rosette', 'XPO:0129634', 'increased size of the somatic stem cell', 0.4186046511627907, 5.43643956286526, 1.5085486027240909, 'HP:0025461', 'Abnormal cell morphology'),
(465409, 'HP:0031925', 'Rosette', 'XPO:0129787', 'increased size of the oocyte', 0.4186046511627907, 5.43643956286526, 1.5085486027240909, 'HP:0025461', 'Abnormal cell morphology'),
(465410, 'HP:0031925', 'Rosette', 'XPO:0101513', 'abnormal basal body', 0.52, 3.6715585125471644, 1.3817418089225373, 'UPHENO:0086172', 'abnormal cell'),
(465411, 'HP:0031925', 'Rosette', 'XPO:0102455', 'abnormal blood morphology', 0.42424242424242425, 2.7446671847279203, 1.0790756508176813, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(465412, 'HP:0031925', 'Rosette', 'XPO:0141289', 'abnormal spindle microtubule morphology', 0.5161290322580645, 3.6715585125471644, 1.376589242279565, 'UPHENO:0086172', 'abnormal cell'),
(465413, 'HP:0031925', 'Rosette', 'XPO:0103147', 'abnormal neuromast mantle cell morphology', 0.43902439024390244, 5.43643956286526, 1.5449043867452603, 'HP:0025461', 'Abnormal cell morphology'),
(465414, 'HP:0031925', 'Rosette', 'XPO:0103084', 'abnormal blastomere V1.1.1 morphology', 0.43902439024390244, 5.43643956286526, 1.5449043867452603, 'HP:0025461', 'Abnormal cell morphology'),
(465415, 'HP:0031925', 'Rosette', 'XPO:0101113', 'abnormal stage IV oocyte', 0.5, 3.6715585125471644, 1.3549093166236559, 'UPHENO:0086172', 'abnormal cell'),
(465416, 'HP:0031925', 'Rosette', 'XPO:0100704', 'abnormal Merkel cell', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(465417, 'HP:0031925', 'Rosette', 'XPO:0125013', 'absent early embryonic cell', 0.4117647058823529, 3.6715585125471644, 1.229560169755361, 'UPHENO:0086172', 'abnormal cell'),
(465418, 'HP:0031925', 'Rosette', 'XPO:0103207', 'abnormal vitelline membrane morphology', 0.48484848484848486, 3.6715585125471644, 1.3342224633999569, 'UPHENO:0086172', 'abnormal cell'),
(465419, 'HP:0031925', 'Rosette', 'XPO:0125854', 'absent barrier epithelial cell', 0.42424242424242425, 3.6715585125471644, 1.2480508339450433, 'UPHENO:0086172', 'abnormal cell'),
(465420, 'HP:0031925', 'Rosette', 'XPO:0102394', 'abnormal intersomitic region morphology', 0.41379310344827586, 2.7446671847279203, 1.0657036887902793, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(465421, 'HP:0031925', 'Rosette', 'XPO:0102061', 'abnormal spermatid morphology', 0.6, 5.43643956286526, 1.8060630492092893, 'HP:0025461', 'Abnormal cell morphology'),
(465422, 'HP:0031925', 'Rosette', 'XPO:0100392', 'abnormal cilium', 0.5, 3.6715585125471644, 1.3549093166236559, 'UPHENO:0086172', 'abnormal cell'),
(465423, 'HP:0031925', 'Rosette', 'XPO:0130930', 'increased size of the yolk platelet', 0.43243243243243246, 3.6715585125471644, 1.2600400701560144, 'UPHENO:0086172', 'abnormal cell'),
(465424, 'HP:0031925', 'Rosette', 'XPO:0128563', 'decreased size of the primordial germ cell', 0.4186046511627907, 5.43643956286526, 1.5085486027240909, 'HP:0025461', 'Abnormal cell morphology'),
(465425, 'HP:0031925', 'Rosette', 'XPO:0141068', 'abnormally necrotic natural killer cell', 0.4090909090909091, 5.43643956286526, 1.491307481034791, 'HP:0025461', 'Abnormal cell morphology'),
(465426, 'HP:0031925', 'Rosette', 'XPO:0107373', 'abnormal efferent neuron morphology', 0.47368421052631576, 5.43643956286526, 1.6047291305419304, 'HP:0025461', 'Abnormal cell morphology'),
(465427, 'HP:0031925', 'Rosette', 'XPO:0125743', 'absent lampbrush chromosome', 0.42424242424242425, 3.6715585125471644, 1.2480508339450433, 'UPHENO:0086172', 'abnormal cell'),
(465428, 'HP:0031925', 'Rosette', 'XPO:0140566', 'abnormally necrotic apical region', 0.41379310344827586, 2.7446671847279203, 1.0657036887902793, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(465429, 'HP:0031925', 'Rosette', 'XPO:0131591', 'decreased size of the Roux spot', 0.43243243243243246, 3.6715585125471644, 1.2600400701560144, 'UPHENO:0086172', 'abnormal cell'),
(465430, 'HP:0031925', 'Rosette', 'XPO:0129433', 'decreased size of the mucus secreting cell', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(465431, 'HP:0031925', 'Rosette', 'XPO:0101646', 'abnormal tissue morphology', 0.42857142857142855, 2.7446671847279203, 1.0845671654222093, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(465432, 'HP:0031925', 'Rosette', 'XPO:0102979', 'abnormal hindlimb region morphology', 0.4444444444444444, 2.7446671847279203, 1.104469140402437, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(465433, 'HP:0031925', 'Rosette', 'XPO:0101373', 'abnormal oxygen accumulating cell', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(465434, 'HP:0031925', 'Rosette', 'XPO:0140314', 'abnormally necrotic right blastomere', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(465435, 'HP:0031925', 'Rosette', 'XPO:0129425', 'decreased size of the microtubule', 0.45714285714285713, 3.6715585125471644, 1.2955411026258445, 'UPHENO:0086172', 'abnormal cell'),
(465436, 'HP:0031925', 'Rosette', 'XPO:0131248', 'abnormally decreased number of acid secreting cell', 0.4117647058823529, 3.6715585125471644, 1.229560169755361, 'UPHENO:0086172', 'abnormal cell'),
(465437, 'HP:0031925', 'Rosette', 'XPO:0131685', 'abnormal cortical actin cytoskeleton', 0.5, 3.6715585125471644, 1.3549093166236559, 'UPHENO:0086172', 'abnormal cell'),
(465438, 'HP:0031925', 'Rosette', 'XPO:0100862', 'abnormal blastomere V1', 0.48148148148148145, 3.6715585125471644, 1.3295816755533123, 'UPHENO:0086172', 'abnormal cell'),
(465439, 'HP:0031925', 'Rosette', 'XPO:0100533', 'abnormal melanoblast', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(465440, 'HP:0031925', 'Rosette', 'XPO:0127533', 'abnormally localised spermatocyte', 0.42424242424242425, 3.6715585125471644, 1.2480508339450433, 'UPHENO:0086172', 'abnormal cell'),
(465441, 'HP:0031925', 'Rosette', 'XPO:0129392', 'decreased size of the barrier epithelial cell', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(465442, 'HP:0031925', 'Rosette', 'XPO:0124884', 'absent keratin accumulating cell', 0.42424242424242425, 3.6715585125471644, 1.2480508339450433, 'UPHENO:0086172', 'abnormal cell'),
(465443, 'HP:0031925', 'Rosette', 'XPO:0131061', 'abnormally increased number of keratin accumulating cell', 0.42424242424242425, 3.6715585125471644, 1.2480508339450433, 'UPHENO:0086172', 'abnormal cell'),
(465444, 'HP:0031925', 'Rosette', 'XPO:0131597', 'decreased size of the spindle microtubule', 0.42105263157894735, 3.6715585125471644, 1.2433500608051093, 'UPHENO:0086172', 'abnormal cell'),
(465445, 'HP:0031925', 'Rosette', 'XPO:0100307', 'abnormal blastomere', 0.5, 3.6715585125471644, 1.3549093166236559, 'UPHENO:0086172', 'abnormal cell'),
(465446, 'HP:0031925', 'Rosette', 'XPO:0101890', 'abnormal organ part morphology', 0.48, 2.7446671847279203, 1.1477979999413668, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(465447, 'HP:0031925', 'Rosette', 'XPO:0127089', 'abnormally localised myoblast', 0.45161290322580644, 3.6715585125471644, 1.2876813267322194, 'UPHENO:0086172', 'abnormal cell'),
(465448, 'HP:0031925', 'Rosette', 'XPO:0101241', 'abnormal nucleate erythrocyte', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(465449, 'HP:0031925', 'Rosette', 'XPO:0130381', 'increased size of the multiciliated cell', 0.4186046511627907, 5.43643956286526, 1.5085486027240909, 'HP:0025461', 'Abnormal cell morphology'),
(465450, 'HP:0031925', 'Rosette', 'XPO:0102654', 'abnormal blastomere V1.2 morphology', 0.43902439024390244, 5.43643956286526, 1.5449043867452603, 'HP:0025461', 'Abnormal cell morphology'),
(465451, 'HP:0031925', 'Rosette', 'XPO:0141203', 'abnormally necrotic exocrine cell', 0.5625, 5.43643956286526, 1.748713027947041, 'HP:0025461', 'Abnormal cell morphology'),
(465452, 'HP:0031925', 'Rosette', 'XPO:0101969', 'abnormal zygote morphology', 0.6428571428571429, 5.43643956286526, 1.869452862390249, 'HP:0025461', 'Abnormal cell morphology'),
(465453, 'HP:0031925', 'Rosette', 'XPO:0129517', 'increased size of the anatomical space', 0.41379310344827586, 2.7446671847279203, 1.0657036887902793, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(465454, 'HP:0031925', 'Rosette', 'XPO:0100515', 'abnormal somatic stem cell', 0.52, 3.6715585125471644, 1.3817418089225373, 'UPHENO:0086172', 'abnormal cell'),
(465455, 'HP:0031925', 'Rosette', 'XPO:0107339', 'abnormal yolk platelet', 0.48148148148148145, 3.6715585125471644, 1.3295816755533123, 'UPHENO:0086172', 'abnormal cell'),
(465456, 'HP:0031925', 'Rosette', 'XPO:0100581', 'abnormal immune system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(465457, 'HP:0031925', 'Rosette', 'XPO:0103041', 'abnormal perivitelline space morphology', 0.5161290322580645, 3.6715585125471644, 1.376589242279565, 'UPHENO:0086172', 'abnormal cell'),
(465458, 'HP:0031925', 'Rosette', 'XPO:0127428', 'abnormally localised endoplasmic reticulum', 0.4375, 3.6715585125471644, 1.2674016132384338, 'UPHENO:0086172', 'abnormal cell'),
(465459, 'HP:0031925', 'Rosette', 'XPO:0130926', 'increased size of the ring structure', 0.43243243243243246, 3.6715585125471644, 1.2600400701560144, 'UPHENO:0086172', 'abnormal cell'),
(465460, 'HP:0031925', 'Rosette', 'XPO:0100549', 'abnormal mitotic cell', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(465461, 'HP:0031925', 'Rosette', 'XPO:0126473', 'abnormally localised germ cell', 0.45161290322580644, 3.6715585125471644, 1.2876813267322194, 'UPHENO:0086172', 'abnormal cell'),
(465462, 'HP:0031925', 'Rosette', 'XPO:0140289', 'abnormally necrotic endodermal cell', 0.42857142857142855, 5.43643956286526, 1.526401870347189, 'HP:0025461', 'Abnormal cell morphology'),
(465463, 'HP:0031925', 'Rosette', 'XPO:0103430', 'decreased size of the apical junction complex', 0.41025641025641024, 3.6715585125471644, 1.2273061620492112, 'UPHENO:0086172', 'abnormal cell'),
(465464, 'HP:0031925', 'Rosette', 'XPO:0140781', 'abnormally necrotic stage I oocyte', 0.47368421052631576, 5.43643956286526, 1.6047291305419304, 'HP:0025461', 'Abnormal cell morphology'),
(465465, 'HP:0031925', 'Rosette', 'XPO:0102965', 'abnormal barrier epithelial cell morphology', 0.6428571428571429, 5.43643956286526, 1.869452862390249, 'HP:0025461', 'Abnormal cell morphology'),
(465466, 'HP:0031925', 'Rosette', 'XPO:0129879', 'increased size of the pericyte', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(465467, 'HP:0031925', 'Rosette', 'XPO:0130121', 'increased size of the centrosome', 0.45714285714285713, 3.6715585125471644, 1.2955411026258445, 'UPHENO:0086172', 'abnormal cell'),
(465468, 'HP:0031925', 'Rosette', 'XPO:0131292', 'abnormally decreased number of mucus secreting cell', 0.4117647058823529, 3.6715585125471644, 1.229560169755361, 'UPHENO:0086172', 'abnormal cell'),
(465469, 'HP:0031925', 'Rosette', 'XPO:0102206', 'abnormal gastrula cell morphology', 0.5625, 5.43643956286526, 1.748713027947041, 'HP:0025461', 'Abnormal cell morphology'),
(465470, 'HP:0031925', 'Rosette', 'XPO:0101497', 'abnormal ciliary axoneme', 0.48148148148148145, 3.6715585125471644, 1.3295816755533123, 'UPHENO:0086172', 'abnormal cell'),
(465471, 'HP:0031925', 'Rosette', 'XPO:0101405', 'abnormal ring structure', 0.48148148148148145, 3.6715585125471644, 1.3295816755533123, 'UPHENO:0086172', 'abnormal cell'),
(465472, 'HP:0031925', 'Rosette', 'XPO:0129360', 'decreased size of the vegetal cortex', 0.42105263157894735, 3.6715585125471644, 1.2433500608051093, 'UPHENO:0086172', 'abnormal cell'),
(465473, 'HP:0031925', 'Rosette', 'XPO:0128267', 'decreased size of the zygote', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(465474, 'HP:0031925', 'Rosette', 'XPO:0100574', 'abnormal gastrula cell', 0.5, 3.6715585125471644, 1.3549093166236559, 'UPHENO:0086172', 'abnormal cell'),
(465475, 'HP:0031925', 'Rosette', 'XPO:0141048', 'abnormally necrotic mitotic cell', 0.5625, 5.43643956286526, 1.748713027947041, 'HP:0025461', 'Abnormal cell morphology'),
(465476, 'HP:0031925', 'Rosette', 'XPO:0127029', 'abnormally localised multiciliated cell precursor', 0.45161290322580644, 3.6715585125471644, 1.2876813267322194, 'UPHENO:0086172', 'abnormal cell'),
(465477, 'HP:0031925', 'Rosette', 'XPO:0140899', 'abnormally necrotic mucus secreting cell', 0.5625, 5.43643956286526, 1.748713027947041, 'HP:0025461', 'Abnormal cell morphology'),
(465478, 'HP:0031925', 'Rosette', 'XPO:0102081', 'abnormal lymphocyte morphology', 0.5294117647058824, 5.43643956286526, 1.696500828969256, 'HP:0025461', 'Abnormal cell morphology'),
(465479, 'HP:0031925', 'Rosette', 'XPO:0102178', 'abnormal whole organism morphology', 0.48, 2.7446671847279203, 1.1477979999413668, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(465480, 'HP:0031925', 'Rosette', 'XPO:0131708', 'abnormal cilium disassembly', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(465481, 'HP:0031925', 'Rosette', 'XPO:0133473', 'abnormally decreased number of cilium in the ciliated non-epidermal cell', 0.4117647058823529, 3.6715585125471644, 1.229560169755361, 'UPHENO:0086172', 'abnormal cell'),
(465482, 'HP:0031925', 'Rosette', 'XPO:0129139', 'decreased size of the kinetochore', 0.45714285714285713, 3.6715585125471644, 1.2955411026258445, 'UPHENO:0086172', 'abnormal cell'),
(465483, 'HP:0031925', 'Rosette', 'XPO:0107359', 'abnormal axial region morphology', 0.4444444444444444, 2.7446671847279203, 1.104469140402437, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(465484, 'HP:0031925', 'Rosette', 'XPO:0100907', 'abnormal cytoplasm', 0.52, 3.6715585125471644, 1.3817418089225373, 'UPHENO:0086172', 'abnormal cell'),
(465485, 'HP:0031925', 'Rosette', 'XPO:0125833', 'absent kinetochore', 0.42424242424242425, 3.6715585125471644, 1.2480508339450433, 'UPHENO:0086172', 'abnormal cell'),
(465486, 'HP:0031925', 'Rosette', 'XPO:0140123', 'abnormally necrotic perichondrial cell', 0.4186046511627907, 5.43643956286526, 1.5085486027240909, 'HP:0025461', 'Abnormal cell morphology'),
(465487, 'HP:0031925', 'Rosette', 'XPO:0131145', 'abnormally increased number of polar body', 0.42424242424242425, 3.6715585125471644, 1.2480508339450433, 'UPHENO:0086172', 'abnormal cell'),
(465488, 'HP:0031925', 'Rosette', 'XPO:0102336', 'abnormal Merkel cell morphology', 0.6428571428571429, 5.43643956286526, 1.869452862390249, 'HP:0025461', 'Abnormal cell morphology'),
(465489, 'HP:0031925', 'Rosette', 'XPO:0127364', 'abnormally localised multiciliated cell', 0.42424242424242425, 3.6715585125471644, 1.2480508339450433, 'UPHENO:0086172', 'abnormal cell'),
(465490, 'HP:0031925', 'Rosette', 'XPO:0142065', 'abnormally decreased number of desmosome', 0.45161290322580644, 3.6715585125471644, 1.2876813267322194, 'UPHENO:0086172', 'abnormal cell'),
(465491, 'HP:0031925', 'Rosette', 'XPO:0103636', 'abnormally increased number of melanoblast', 0.42424242424242425, 3.6715585125471644, 1.2480508339450433, 'UPHENO:0086172', 'abnormal cell'),
(465492, 'HP:0031925', 'Rosette', 'XPO:0103753', 'increased size of the apical junction complex', 0.41025641025641024, 3.6715585125471644, 1.2273061620492112, 'UPHENO:0086172', 'abnormal cell'),
(465493, 'HP:0031925', 'Rosette', 'XPO:0101009', 'abnormal blastomere D1.1.1', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(465494, 'HP:0031925', 'Rosette', 'XPO:0130465', 'increased size of the migrating myoblast', 0.4186046511627907, 5.43643956286526, 1.5085486027240909, 'HP:0025461', 'Abnormal cell morphology'),
(465495, 'HP:0031925', 'Rosette', 'XPO:0130042', 'increased size of the mesenchymal stem cell', 0.4186046511627907, 5.43643956286526, 1.5085486027240909, 'HP:0025461', 'Abnormal cell morphology'),
(465496, 'HP:0031925', 'Rosette', 'XPO:0126737', 'abnormally localised mesenchymal stem cell', 0.42424242424242425, 3.6715585125471644, 1.2480508339450433, 'UPHENO:0086172', 'abnormal cell'),
(465497, 'HP:0031925', 'Rosette', 'XPO:0101452', 'abnormal blastomere V1.1.1', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(465498, 'HP:0031925', 'Rosette', 'XPO:0128557', 'decreased size of the secondary oogonium', 0.4186046511627907, 5.43643956286526, 1.5085486027240909, 'HP:0025461', 'Abnormal cell morphology'),
(465499, 'HP:0031925', 'Rosette', 'XPO:0101037', 'abnormal hatching gland cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(465500, 'HP:0031925', 'Rosette', 'XPO:0100503', 'abnormal blastomere D2', 0.48148148148148145, 3.6715585125471644, 1.3295816755533123, 'UPHENO:0086172', 'abnormal cell'),
(465501, 'HP:0031925', 'Rosette', 'XPO:0131371', 'abnormally decreased number of electrically active cell', 0.4117647058823529, 3.6715585125471644, 1.229560169755361, 'UPHENO:0086172', 'abnormal cell'),
(465502, 'HP:0031925', 'Rosette', 'XPO:0127794', 'abnormally localised mitotic cell', 0.45161290322580644, 3.6715585125471644, 1.2876813267322194, 'UPHENO:0086172', 'abnormal cell'),
(465503, 'HP:0031925', 'Rosette', 'XPO:0102794', 'abnormal stromal cell morphology', 0.5294117647058824, 5.43643956286526, 1.696500828969256, 'HP:0025461', 'Abnormal cell morphology'),
(465504, 'HP:0031925', 'Rosette', 'XPO:0102356', 'abnormal kinetochore morphology', 0.5517241379310345, 3.6715585125471644, 1.423266473714053, 'UPHENO:0086172', 'abnormal cell'),
(465505, 'HP:0031925', 'Rosette', 'XPO:0101850', 'abnormal epithelial cell morphology', 0.5806451612903226, 5.43643956286526, 1.776694213089295, 'HP:0025461', 'Abnormal cell morphology'),
(465506, 'HP:0031925', 'Rosette', 'XPO:0102491', 'abnormal blastomere V1.1.2 morphology', 0.43902439024390244, 5.43643956286526, 1.5449043867452603, 'HP:0025461', 'Abnormal cell morphology'),
(465507, 'HP:0031925', 'Rosette', 'XPO:0140269', 'abnormally necrotic anatomical line', 0.48, 2.7446671847279203, 1.1477979999413668, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(465508, 'HP:0031925', 'Rosette', 'XPO:0102353', 'abnormal centromere morphology', 0.5517241379310345, 3.6715585125471644, 1.423266473714053, 'UPHENO:0086172', 'abnormal cell'),
(465509, 'HP:0031925', 'Rosette', 'XPO:0103208', 'abnormal blastomere V1.2.2 morphology', 0.43902439024390244, 5.43643956286526, 1.5449043867452603, 'HP:0025461', 'Abnormal cell morphology'),
(465510, 'HP:0031925', 'Rosette', 'XPO:0102703', 'abnormal endoplasmic reticulum morphology', 0.5517241379310345, 3.6715585125471644, 1.423266473714053, 'UPHENO:0086172', 'abnormal cell'),
(465511, 'HP:0031925', 'Rosette', 'XPO:0131110', 'abnormally increased number of paracrine cell', 0.42424242424242425, 3.6715585125471644, 1.2480508339450433, 'UPHENO:0086172', 'abnormal cell'),
(465512, 'HP:0031925', 'Rosette', 'XPO:0102177', 'abnormal male organism morphology', 0.4444444444444444, 2.7446671847279203, 1.104469140402437, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(465513, 'HP:0031925', 'Rosette', 'XPO:0103019', 'abnormal melanophore morphology', 0.4186046511627907, 5.43643956286526, 1.5085486027240909, 'HP:0025461', 'Abnormal cell morphology'),
(465514, 'HP:0031925', 'Rosette', 'XPO:0101240', 'abnormal ciliated non-epidermal cell', 0.52, 3.6715585125471644, 1.3817418089225373, 'UPHENO:0086172', 'abnormal cell'),
(465515, 'HP:0031925', 'Rosette', 'XPO:0141316', 'abnormal anatomical region morphology', 0.48, 2.7446671847279203, 1.1477979999413668, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(465516, 'HP:0031925', 'Rosette', 'XPO:0102830', 'abnormal digestive enzyme secreting cell morphology', 0.46153846153846156, 5.43643956286526, 1.5840220806831131, 'HP:0025461', 'Abnormal cell morphology'),
(465517, 'HP:0031925', 'Rosette', 'XPO:0103166', 'abnormal blastomere V2.1.1 morphology', 0.43902439024390244, 5.43643956286526, 1.5449043867452603, 'HP:0025461', 'Abnormal cell morphology'),
(465518, 'HP:0031925', 'Rosette', 'XPO:0115704', 'abnormally defasciculated motor neuron', 0.47368421052631576, 5.43643956286526, 1.6047291305419304, 'HP:0025461', 'Abnormal cell morphology'),
(465519, 'HP:0031925', 'Rosette', 'XPO:0100006', 'abnormal anatomical structure', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(465520, 'HP:0031925', 'Rosette', 'XPO:0101176', 'abnormal non-ciliated epithelial cell', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(465521, 'HP:0031925', 'Rosette', 'XPO:0131351', 'abnormally decreased number of apoptotic cell', 0.4117647058823529, 3.6715585125471644, 1.229560169755361, 'UPHENO:0086172', 'abnormal cell'),
(465522, 'HP:0031925', 'Rosette', 'XPO:0130547', 'increased size of the paracrine cell', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(465523, 'HP:0031925', 'Rosette', 'XPO:0139950', 'abnormally necrotic B cell', 0.43902439024390244, 5.43643956286526, 1.5449043867452603, 'HP:0025461', 'Abnormal cell morphology'),
(465524, 'HP:0031925', 'Rosette', 'XPO:0100791', 'abnormal multiciliated cell precursor', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(465525, 'HP:0031925', 'Rosette', 'XPO:0100969', 'abnormal disaggregated/reaggregated ectoderm treated with activin', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(465526, 'HP:0031925', 'Rosette', 'XPO:0128007', 'decreased size of the anatomical structure', 0.4444444444444444, 2.7446671847279203, 1.104469140402437, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(465527, 'HP:0031925', 'Rosette', 'XPO:0127339', 'abnormally localised migrating myoblast', 0.42424242424242425, 3.6715585125471644, 1.2480508339450433, 'UPHENO:0086172', 'abnormal cell'),
(465528, 'HP:0031925', 'Rosette', 'XPO:0107311', 'abnormal apical junction complex', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(465529, 'HP:0031925', 'Rosette', 'XPO:0129015', 'decreased size of the spermatid', 0.4186046511627907, 5.43643956286526, 1.5085486027240909, 'HP:0025461', 'Abnormal cell morphology'),
(465530, 'HP:0031925', 'Rosette', 'XPO:0131346', 'abnormally decreased number of chondroblast', 0.4117647058823529, 3.6715585125471644, 1.229560169755361, 'UPHENO:0086172', 'abnormal cell'),
(465531, 'HP:0031925', 'Rosette', 'XPO:0140096', 'abnormally necrotic gastrula cell', 0.4864864864864865, 5.43643956286526, 1.626270082715184, 'HP:0025461', 'Abnormal cell morphology'),
(465532, 'HP:0031925', 'Rosette', 'XPO:0141154', 'abnormally necrotic barrier cell', 0.5625, 5.43643956286526, 1.748713027947041, 'HP:0025461', 'Abnormal cell morphology'),
(465533, 'HP:0031925', 'Rosette', 'XPO:0103894', 'abnormally decreased number of spindle microtubule', 0.4375, 3.6715585125471644, 1.2674016132384338, 'UPHENO:0086172', 'abnormal cell'),
(465534, 'HP:0031925', 'Rosette', 'XPO:0129376', 'decreased size of the lampbrush chromosome', 0.45714285714285713, 3.6715585125471644, 1.2955411026258445, 'UPHENO:0086172', 'abnormal cell'),
(465535, 'HP:0031925', 'Rosette', 'XPO:0107398', 'abnormal apical junction complex morphology', 0.48484848484848486, 3.6715585125471644, 1.3342224633999569, 'UPHENO:0086172', 'abnormal cell'),
(465536, 'HP:0031925', 'Rosette', 'XPO:0140278', 'abnormally necrotic Merkel cell', 0.5625, 5.43643956286526, 1.748713027947041, 'HP:0025461', 'Abnormal cell morphology'),
(465537, 'HP:0031925', 'Rosette', 'XPO:0141246', 'abnormally necrotic stage V oocyte', 0.47368421052631576, 5.43643956286526, 1.6047291305419304, 'HP:0025461', 'Abnormal cell morphology'),
(465538, 'HP:0031925', 'Rosette', 'XPO:0107352', 'abnormal posterior side morphology', 0.41379310344827586, 2.7446671847279203, 1.0657036887902793, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(465539, 'HP:0031925', 'Rosette', 'XPO:0129862', 'increased size of the myoblast', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(465540, 'HP:0031925', 'Rosette', 'XPO:0140723', 'abnormally necrotic polar body', 0.4186046511627907, 5.43643956286526, 1.5085486027240909, 'HP:0025461', 'Abnormal cell morphology'),
(465541, 'HP:0031925', 'Rosette', 'XPO:0100344', 'abnormal portion of organism substance', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(465542, 'HP:0031925', 'Rosette', 'XPO:0103010', 'abnormal blastomere D1 morphology', 0.5294117647058824, 5.43643956286526, 1.696500828969256, 'HP:0025461', 'Abnormal cell morphology'),
(465543, 'HP:0031925', 'Rosette', 'XPO:0102176', 'abnormal neuromast support cell morphology', 0.43902439024390244, 5.43643956286526, 1.5449043867452603, 'HP:0025461', 'Abnormal cell morphology'),
(465544, 'HP:0031925', 'Rosette', 'XPO:0101074', 'abnormal germinal vesicle', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(465545, 'HP:0031925', 'Rosette', 'XPO:0101534', 'abnormal blastomere V2.1.1', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(465546, 'HP:0031925', 'Rosette', 'XPO:0127819', 'abnormally localised ciliary axoneme', 0.4117647058823529, 3.6715585125471644, 1.229560169755361, 'UPHENO:0086172', 'abnormal cell'),
(465547, 'HP:0031925', 'Rosette', 'XPO:0130238', 'increased size of the oocyte cortex', 0.43243243243243246, 3.6715585125471644, 1.2600400701560144, 'UPHENO:0086172', 'abnormal cell'),
(465548, 'HP:0031925', 'Rosette', 'XPO:0102113', 'abnormal anatomical line morphology', 0.5217391304347826, 2.7446671847279203, 1.196662137068282, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(465549, 'HP:0031925', 'Rosette', 'XPO:0131626', 'increased size of the adherens junction', 0.45714285714285713, 3.6715585125471644, 1.2955411026258445, 'UPHENO:0086172', 'abnormal cell'),
(465550, 'HP:0031925', 'Rosette', 'XPO:0101664', 'abnormal nervous system morphology', 0.4117647058823529, 2.7446671847279203, 1.0630884610720022, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(465551, 'HP:0031925', 'Rosette', 'XPO:0100675', 'abnormal dorsal vegetal hemisphere blastomere', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(465552, 'HP:0031925', 'Rosette', 'XPO:0102141', 'abnormal germ plasm morphology', 0.47058823529411764, 3.6715585125471644, 1.3144551118994765, 'UPHENO:0086172', 'abnormal cell'),
(465553, 'HP:0031925', 'Rosette', 'XPO:0141091', 'abnormally necrotic posterior region', 0.42857142857142855, 2.7446671847279203, 1.0845671654222093, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(465554, 'HP:0031925', 'Rosette', 'XPO:0129070', 'decreased size of the paracrine cell', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(465555, 'HP:0031925', 'Rosette', 'XPO:0130337', 'increased size of the nucleus', 0.45714285714285713, 3.6715585125471644, 1.2955411026258445, 'UPHENO:0086172', 'abnormal cell'),
(465556, 'HP:0031925', 'Rosette', 'XPO:0139923', 'abnormally necrotic acellular anatomical structure', 0.41379310344827586, 2.7446671847279203, 1.0657036887902793, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(465557, 'HP:0031925', 'Rosette', 'XPO:0101641', 'abnormal multi-tissue structure morphology', 0.42857142857142855, 2.7446671847279203, 1.0845671654222093, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(465558, 'HP:0031925', 'Rosette', 'XPO:0125394', 'absent multiciliated cell precursor', 0.42424242424242425, 3.6715585125471644, 1.2480508339450433, 'UPHENO:0086172', 'abnormal cell'),
(465559, 'HP:0031925', 'Rosette', 'XPO:0140389', 'abnormally necrotic cell condensation', 0.41379310344827586, 2.7446671847279203, 1.0657036887902793, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(465560, 'HP:0031925', 'Rosette', 'XPO:0131588', 'decreased size of the adherens junction', 0.45714285714285713, 3.6715585125471644, 1.2955411026258445, 'UPHENO:0086172', 'abnormal cell'),
(465561, 'HP:0031925', 'Rosette', 'XPO:0107374', 'abnormal afferent neuron morphology', 0.47368421052631576, 5.43643956286526, 1.6047291305419304, 'HP:0025461', 'Abnormal cell morphology'),
(465562, 'HP:0031925', 'Rosette', 'XPO:0102994', 'abnormal vegetal cortex morphology', 0.5, 3.6715585125471644, 1.3549093166236559, 'UPHENO:0086172', 'abnormal cell'),
(465563, 'HP:0031925', 'Rosette', 'XPO:0103433', 'decreased size of the germ cell', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(465564, 'HP:0031925', 'Rosette', 'XPO:0125693', 'absent mucus secreting cell', 0.42424242424242425, 3.6715585125471644, 1.2480508339450433, 'UPHENO:0086172', 'abnormal cell'),
(465565, 'HP:0031925', 'Rosette', 'XPO:0107258', 'abnormal anatomical axis', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(465566, 'HP:0031925', 'Rosette', 'XPO:0139902', 'abnormally necrotic endocrine cell', 0.46153846153846156, 5.43643956286526, 1.5840220806831131, 'HP:0025461', 'Abnormal cell morphology'),
(465567, 'HP:0031925', 'Rosette', 'XPO:0101940', 'abnormal early embryonic cell morphology', 0.6, 5.43643956286526, 1.8060630492092893, 'HP:0025461', 'Abnormal cell morphology'),
(465568, 'HP:0031925', 'Rosette', 'XPO:0141151', 'abnormally necrotic dorsolateral commissural neuron', 0.42857142857142855, 5.43643956286526, 1.526401870347189, 'HP:0025461', 'Abnormal cell morphology'),
(465569, 'HP:0031925', 'Rosette', 'XPO:0100842', 'abnormal left-dorsal blastomere', 0.48148148148148145, 3.6715585125471644, 1.3295816755533123, 'UPHENO:0086172', 'abnormal cell'),
(465570, 'HP:0031925', 'Rosette', 'XPO:0102773', 'abnormal Keller explant morphology', 0.48, 2.7446671847279203, 1.1477979999413668, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(465571, 'HP:0031925', 'Rosette', 'XPO:0133451', 'decreased size of the cilium in the ciliated non-epidermal cell', 0.41025641025641024, 3.6715585125471644, 1.2273061620492112, 'UPHENO:0086172', 'abnormal cell'),
(465572, 'HP:0031925', 'Rosette', 'XPO:0131589', 'decreased size of the actin cytoskeleton', 0.45714285714285713, 3.6715585125471644, 1.2955411026258445, 'UPHENO:0086172', 'abnormal cell'),
(465573, 'HP:0031925', 'Rosette', 'XPO:0101871', 'abnormal acellular anatomical structure morphology', 0.46153846153846156, 2.7446671847279203, 1.125508538339192, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(465574, 'HP:0031925', 'Rosette', 'XPO:0126681', 'abnormally localised basal body', 0.4375, 3.6715585125471644, 1.2674016132384338, 'UPHENO:0086172', 'abnormal cell'),
(465575, 'HP:0031925', 'Rosette', 'XPO:0128562', 'decreased size of the mesenchymal stem cell', 0.4186046511627907, 5.43643956286526, 1.5085486027240909, 'HP:0025461', 'Abnormal cell morphology'),
(465576, 'HP:0031925', 'Rosette', 'XPO:0102669', 'abnormal hatching gland cell morphology', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(465577, 'HP:0031925', 'Rosette', 'XPO:0130222', 'increased size of the nucleate erythrocyte', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(465578, 'HP:0031925', 'Rosette', 'XPO:0107351', 'abnormal anterior side morphology', 0.41379310344827586, 2.7446671847279203, 1.0657036887902793, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(465579, 'HP:0031925', 'Rosette', 'XPO:0126783', 'abnormally localised exocrine cell', 0.45161290322580644, 3.6715585125471644, 1.2876813267322194, 'UPHENO:0086172', 'abnormal cell'),
(465580, 'HP:0031925', 'Rosette', 'XPO:0101660', 'abnormal anatomical cluster morphology', 0.42857142857142855, 2.7446671847279203, 1.0845671654222093, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(465581, 'HP:0031925', 'Rosette', 'XPO:0102990', 'abnormal endothelial cell morphology', 0.42857142857142855, 5.43643956286526, 1.526401870347189, 'HP:0025461', 'Abnormal cell morphology'),
(465582, 'HP:0031925', 'Rosette', 'XPO:0100954', 'abnormal neural progenitor cell', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(465583, 'HP:0031925', 'Rosette', 'XPO:0130817', 'increased size of the centromere', 0.45714285714285713, 3.6715585125471644, 1.2955411026258445, 'UPHENO:0086172', 'abnormal cell'),
(465584, 'HP:0031925', 'Rosette', 'XPO:0130882', 'increased size of the exocrine cell', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(465585, 'HP:0031925', 'Rosette', 'XPO:0131075', 'abnormally increased number of mucus secreting cell', 0.42424242424242425, 3.6715585125471644, 1.2480508339450433, 'UPHENO:0086172', 'abnormal cell'),
(465586, 'HP:0031925', 'Rosette', 'XPO:0102135', 'abnormal blastomere D2 morphology', 0.5294117647058824, 5.43643956286526, 1.696500828969256, 'HP:0025461', 'Abnormal cell morphology'),
(465587, 'HP:0031925', 'Rosette', 'XPO:0140395', 'abnormally necrotic antero-dorsal region', 0.42857142857142855, 2.7446671847279203, 1.0845671654222093, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(465588, 'HP:0031925', 'Rosette', 'XPO:0100546', 'abnormal whole organism', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(465589, 'HP:0031925', 'Rosette', 'XPO:0100887', 'abnormal right-dorsal blastomere', 0.48148148148148145, 3.6715585125471644, 1.3295816755533123, 'UPHENO:0086172', 'abnormal cell'),
(465590, 'HP:0031925', 'Rosette', 'XPO:0133483', 'increased size of the cilium in multiciliated cell', 0.41025641025641024, 3.6715585125471644, 1.2273061620492112, 'UPHENO:0086172', 'abnormal cell'),
(465591, 'HP:0031925', 'Rosette', 'XPO:0128154', 'decreased size of the somatic stem cell', 0.4186046511627907, 5.43643956286526, 1.5085486027240909, 'HP:0025461', 'Abnormal cell morphology'),
(465592, 'HP:0031925', 'Rosette', 'XPO:0129582', 'increased size of the portion of organism substance', 0.4444444444444444, 2.7446671847279203, 1.104469140402437, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(465593, 'HP:0031925', 'Rosette', 'XPO:0101004', 'abnormal acid secreting cell', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(465594, 'HP:0031925', 'Rosette', 'XPO:0140364', 'abnormally necrotic anterior region', 0.42857142857142855, 2.7446671847279203, 1.0845671654222093, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(465595, 'HP:0031925', 'Rosette', 'XPO:0100285', 'abnormal progenitor cell', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(465596, 'HP:0031925', 'Rosette', 'XPO:0100032', 'abnormal nervous system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(465597, 'HP:0031925', 'Rosette', 'XPO:0101569', 'abnormal activin-induced ectoderm', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(465598, 'HP:0031925', 'Rosette', 'XPO:0100081', 'abnormal anatomical entity in vitro', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(465599, 'HP:0031925', 'Rosette', 'XPO:0101333', 'abnormal barrier epithelial cell', 0.5416666666666666, 3.6715585125471644, 1.4102343283876786, 'UPHENO:0086172', 'abnormal cell'),
(465600, 'HP:0031925', 'Rosette', 'XPO:0101500', 'abnormal endodermal cell', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(465601, 'HP:0031925', 'Rosette', 'XPO:0142066', 'abnormally increased number of desmosome', 0.4666666666666667, 3.6715585125471644, 1.308966757607698, 'UPHENO:0086172', 'abnormal cell'),
(465602, 'HP:0031925', 'Rosette', 'XPO:0126162', 'absent alkali secreting cell', 0.42424242424242425, 3.6715585125471644, 1.2480508339450433, 'UPHENO:0086172', 'abnormal cell'),
(465603, 'HP:0031925', 'Rosette', 'XPO:0131677', 'abnormal actin filament', 0.5, 3.6715585125471644, 1.3549093166236559, 'UPHENO:0086172', 'abnormal cell'),
(465604, 'HP:0031925', 'Rosette', 'XPO:0139713', 'abnormally necrotic multicellular anatomical structure', 0.41379310344827586, 2.7446671847279203, 1.0657036887902793, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(465605, 'HP:0031925', 'Rosette', 'XPO:0103093', 'abnormal sperm entry point morphology', 0.5333333333333333, 3.6715585125471644, 1.399344325041251, 'UPHENO:0086172', 'abnormal cell'),
(465606, 'HP:0031925', 'Rosette', 'XPO:0130564', 'increased size of the ciliated non-epidermal cell', 0.4186046511627907, 5.43643956286526, 1.5085486027240909, 'HP:0025461', 'Abnormal cell morphology'),
(465607, 'HP:0031925', 'Rosette', 'XPO:0100034', 'abnormal blastomere V1.1', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(465608, 'HP:0031925', 'Rosette', 'XPO:0131171', 'abnormally increased number of barrier epithelial cell', 0.42424242424242425, 3.6715585125471644, 1.2480508339450433, 'UPHENO:0086172', 'abnormal cell'),
(465609, 'HP:0002753', 'Thin bony cortex', 'XPO:0140043', 'abnormally necrotic perichondrium', 0.43137254901960786, 6.985637650836012, 1.7359182929989752, 'UPHENO:0002712', 'abnormal connective tissue'),
(465610, 'HP:0002753', 'Thin bony cortex', 'XPO:0141723', 'abnormal posterior notochord morphology', 0.43478260869565216, 4.638757693672553, 1.4201588541997616, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(465611, 'HP:0002753', 'Thin bony cortex', 'XPO:0128103', 'decreased size of the perichordal tissue', 0.4716981132075472, 6.985637650836012, 1.8152443635640214, 'UPHENO:0002712', 'abnormal connective tissue'),
(465612, 'HP:0002753', 'Thin bony cortex', 'XPO:0102217', 'abnormal elastica externa morphology', 0.45454545454545453, 4.638757693672553, 1.452076521536181, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(465613, 'HP:0002753', 'Thin bony cortex', 'XPO:0128573', 'decreased size of the adipose tissue', 0.40384615384615385, 6.985637650836012, 1.6796198669499611, 'UPHENO:0002712', 'abnormal connective tissue'),
(465614, 'HP:0002753', 'Thin bony cortex', 'XPO:0128816', 'decreased size of the tendon', 0.44642857142857145, 6.985637650836012, 1.7659525013375537, 'UPHENO:0002712', 'abnormal connective tissue'),
(465615, 'HP:0002753', 'Thin bony cortex', 'XPO:0128456', 'decreased size of the vacuolated notochordal tissue', 0.4716981132075472, 6.985637650836012, 1.8152443635640214, 'UPHENO:0002712', 'abnormal connective tissue'),
(465616, 'HP:0002753', 'Thin bony cortex', 'XPO:0128102', 'decreased size of the portion of organism substance', 0.43243243243243246, 5.653868323764771, 1.5636227268424692, 'UPHENO:0012541', 'decreased size of the anatomical entity in the independent continuant'),
(465617, 'HP:0002753', 'Thin bony cortex', 'XPO:0130908', 'increased size of the notochordal sheath', 0.40384615384615385, 4.6864066944795475, 1.3757133854565902, 'UPHENO:0075195', 'abnormal size of anatomical entity'),
(465618, 'HP:0002753', 'Thin bony cortex', 'XPO:0102097', 'abnormal skeletal system morphology', 0.45454545454545453, 4.638757693672553, 1.452076521536181, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(465619, 'HP:0002753', 'Thin bony cortex', 'XPO:0129832', 'increased size of the skeletal system', 0.42, 4.6864066944795475, 1.402957879510789, 'UPHENO:0075195', 'abnormal size of anatomical entity'),
(465620, 'HP:0002753', 'Thin bony cortex', 'XPO:0129427', 'decreased size of the joint', 0.4107142857142857, 5.653868323764771, 1.5238518596365178, 'UPHENO:0012541', 'decreased size of the anatomical entity in the independent continuant'),
(465621, 'HP:0002753', 'Thin bony cortex', 'XPO:0129612', 'increased size of the perichondrium', 0.4423076923076923, 6.985637650836012, 1.7577830550551468, 'UPHENO:0002712', 'abnormal connective tissue'),
(465622, 'HP:0002753', 'Thin bony cortex', 'XPO:0102130', 'abnormal endoskeleton morphology', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(465623, 'HP:0002753', 'Thin bony cortex', 'XPO:0128306', 'decreased size of the articular system', 0.46938775510204084, 5.653868323764771, 1.6290661619880527, 'UPHENO:0012541', 'decreased size of the anatomical entity in the independent continuant'),
(465624, 'HP:0002753', 'Thin bony cortex', 'XPO:0102567', 'abnormal skeleton morphology', 0.43478260869565216, 4.638757693672553, 1.4201588541997616, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(465625, 'HP:0002753', 'Thin bony cortex', 'XPO:0141709', 'increased size of the anterior notochord', 0.40384615384615385, 4.6864066944795475, 1.3757133854565902, 'UPHENO:0075195', 'abnormal size of anatomical entity'),
(465626, 'HP:0002753', 'Thin bony cortex', 'XPO:0102272', 'abnormal notochordal sheath morphology', 0.43478260869565216, 4.638757693672553, 1.4201588541997616, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(465627, 'HP:0002753', 'Thin bony cortex', 'XPO:0102806', 'abnormal articular system morphology', 0.4444444444444444, 4.638757693672553, 1.4358516936218344, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(465628, 'HP:0002753', 'Thin bony cortex', 'XPO:0102010', 'abnormal perichondrium morphology', 0.4888888888888889, 6.985637650836012, 1.8480261441055443, 'UPHENO:0002712', 'abnormal connective tissue'),
(465629, 'HP:0002753', 'Thin bony cortex', 'XPO:0128890', 'decreased size of the elastica externa', 0.4791666666666667, 5.653868323764771, 1.645948127515147, 'UPHENO:0012541', 'decreased size of the anatomical entity in the independent continuant'),
(465630, 'HP:0002753', 'Thin bony cortex', 'XPO:0128104', 'decreased size of the connective tissue', 0.44680851063829785, 6.985637650836012, 1.7667038106680069, 'UPHENO:0002712', 'abnormal connective tissue'),
(465631, 'HP:0002753', 'Thin bony cortex', 'XPO:0141719', 'abnormal anterior notochord morphology', 0.43478260869565216, 4.638757693672553, 1.4201588541997616, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(465632, 'HP:0002753', 'Thin bony cortex', 'XPO:0128196', 'decreased size of the appendicular skeleton', 0.4107142857142857, 5.653868323764771, 1.5238518596365178, 'UPHENO:0012541', 'decreased size of the anatomical entity in the independent continuant'),
(465633, 'HP:0002753', 'Thin bony cortex', 'XPO:0139806', 'abnormally necrotic vacuolated notochordal tissue', 0.4074074074074074, 6.985637650836012, 1.6870093433098323, 'UPHENO:0002712', 'abnormal connective tissue'),
(465634, 'HP:0002753', 'Thin bony cortex', 'XPO:0129583', 'increased size of the perichordal tissue', 0.41818181818181815, 6.985637650836012, 1.7091713354681468, 'UPHENO:0002712', 'abnormal connective tissue'),
(465635, 'HP:0002753', 'Thin bony cortex', 'XPO:0128071', 'decreased size of the cell part', 0.4090909090909091, 5.653868323764771, 1.5208373129461366, 'UPHENO:0012541', 'decreased size of the anatomical entity in the independent continuant'),
(465636, 'HP:0002753', 'Thin bony cortex', 'XPO:0139792', 'abnormally necrotic perichordal tissue', 0.4074074074074074, 6.985637650836012, 1.6870093433098323, 'UPHENO:0002712', 'abnormal connective tissue'),
(465637, 'HP:0002753', 'Thin bony cortex', 'XPO:0101860', 'abnormal skeletal subdivision morphology', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(465638, 'HP:0002753', 'Thin bony cortex', 'XPO:0102980', 'abnormal perichordal tissue morphology', 0.4583333333333333, 6.985637650836012, 1.7893436198691701, 'UPHENO:0002712', 'abnormal connective tissue'),
(465639, 'HP:0002753', 'Thin bony cortex', 'XPO:0128132', 'decreased size of the perichondrium', 0.5, 6.985637650836012, 1.8689084582766504, 'UPHENO:0002712', 'abnormal connective tissue'),
(465640, 'HP:0002753', 'Thin bony cortex', 'XPO:0129786', 'increased size of the articular system', 0.4117647058823529, 4.6864066944795475, 1.389135297297373, 'UPHENO:0075195', 'abnormal size of anatomical entity'),
(465641, 'HP:0002753', 'Thin bony cortex', 'XPO:0107372', 'abnormal flexural organ morphology', 0.43478260869565216, 4.638757693672553, 1.4201588541997616, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(465642, 'HP:0002753', 'Thin bony cortex', 'XPO:0140123', 'abnormally necrotic perichondrial cell', 0.41509433962264153, 6.985637650836012, 1.7028501541582675, 'UPHENO:0002712', 'abnormal connective tissue'),
(465643, 'HP:0002753', 'Thin bony cortex', 'XPO:0130368', 'increased size of the elastica externa', 0.42, 4.6864066944795475, 1.402957879510789, 'UPHENO:0075195', 'abnormal size of anatomical entity'),
(465644, 'HP:0002753', 'Thin bony cortex', 'XPO:0128007', 'decreased size of the anatomical structure', 0.43243243243243246, 5.653868323764771, 1.5636227268424692, 'UPHENO:0012541', 'decreased size of the anatomical entity in the independent continuant'),
(465645, 'HP:0002753', 'Thin bony cortex', 'XPO:0102009', 'abnormal connective tissue morphology', 0.4186046511627907, 6.985637650836012, 1.710035207818209, 'UPHENO:0002712', 'abnormal connective tissue'),
(465646, 'HP:0002753', 'Thin bony cortex', 'XPO:0129286', 'decreased size of the perichondrial cell', 0.43103448275862066, 6.985637650836012, 1.735237940908176, 'UPHENO:0002712', 'abnormal connective tissue'),
(465647, 'HP:0002753', 'Thin bony cortex', 'XPO:0141713', 'increased size of the posterior notochord', 0.40384615384615385, 4.6864066944795475, 1.3757133854565902, 'UPHENO:0075195', 'abnormal size of anatomical entity'),
(465648, 'HP:0002753', 'Thin bony cortex', 'XPO:0102728', 'abnormal tendon morphology', 0.44, 6.985637650836012, 1.753191537273622, 'UPHENO:0002712', 'abnormal connective tissue'),
(465649, 'HP:0002753', 'Thin bony cortex', 'XPO:0128184', 'decreased size of the skeleton', 0.46, 5.653868323764771, 1.6126932222006127, 'UPHENO:0012541', 'decreased size of the anatomical entity in the independent continuant'),
(465650, 'HP:0002753', 'Thin bony cortex', 'XPO:0141704', 'decreased size of the anterior notochord', 0.46, 5.653868323764771, 1.6126932222006127, 'UPHENO:0012541', 'decreased size of the anatomical entity in the independent continuant'),
(465651, 'HP:0002753', 'Thin bony cortex', 'XPO:0128352', 'decreased size of the skeletal system', 0.4791666666666667, 5.653868323764771, 1.645948127515147, 'UPHENO:0012541', 'decreased size of the anatomical entity in the independent continuant'),
(465652, 'HP:0002753', 'Thin bony cortex', 'XPO:0102542', 'abnormal vacuolated notochordal tissue morphology', 0.4583333333333333, 6.985637650836012, 1.7893436198691701, 'UPHENO:0002712', 'abnormal connective tissue'),
(465653, 'HP:0002753', 'Thin bony cortex', 'XPO:0103574', 'decreased length of notochord', 0.4107142857142857, 5.653868323764771, 1.5238518596365178, 'UPHENO:0012541', 'decreased size of the anatomical entity in the independent continuant'),
(465654, 'HP:0002753', 'Thin bony cortex', 'XPO:0102605', 'abnormal dermal skeleton morphology', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(465655, 'HP:0002753', 'Thin bony cortex', 'XPO:0130188', 'increased size of the flexural organ', 0.40384615384615385, 4.6864066944795475, 1.3757133854565902, 'UPHENO:0075195', 'abnormal size of anatomical entity'),
(465656, 'HP:0002753', 'Thin bony cortex', 'XPO:0129936', 'increased size of the vacuolated notochordal tissue', 0.41818181818181815, 6.985637650836012, 1.7091713354681468, 'UPHENO:0002712', 'abnormal connective tissue'),
(465657, 'HP:0002753', 'Thin bony cortex', 'XPO:0128767', 'decreased size of the dense regular connective tissue', 0.42, 6.985637650836012, 1.7128828953991937, 'UPHENO:0002712', 'abnormal connective tissue'),
(465658, 'HP:0002753', 'Thin bony cortex', 'XPO:0128158', 'decreased size of the skeletal subdivision', 0.45098039215686275, 5.653868323764771, 1.5968042315370725, 'UPHENO:0012541', 'decreased size of the anatomical entity in the independent continuant'),
(465659, 'HP:0002753', 'Thin bony cortex', 'XPO:0129434', 'decreased size of the notochordal sheath', 0.46, 5.653868323764771, 1.6126932222006127, 'UPHENO:0012541', 'decreased size of the anatomical entity in the independent continuant'),
(465660, 'HP:0002753', 'Thin bony cortex', 'XPO:0128709', 'decreased size of the flexural organ', 0.46, 5.653868323764771, 1.6126932222006127, 'UPHENO:0012541', 'decreased size of the anatomical entity in the independent continuant'),
(465661, 'HP:0002753', 'Thin bony cortex', 'XPO:0128397', 'decreased size of the cranial skeleton', 0.4107142857142857, 5.653868323764771, 1.5238518596365178, 'UPHENO:0012541', 'decreased size of the anatomical entity in the independent continuant'),
(465662, 'HP:0002753', 'Thin bony cortex', 'XPO:0128502', 'decreased size of the anatomical line', 0.43243243243243246, 5.653868323764771, 1.5636227268424692, 'UPHENO:0012541', 'decreased size of the anatomical entity in the independent continuant'),
(465663, 'HP:0002753', 'Thin bony cortex', 'XPO:0129010', 'decreased size of the endoskeleton', 0.42592592592592593, 5.653868323764771, 1.5518147765963477, 'UPHENO:0012541', 'decreased size of the anatomical entity in the independent continuant'),
(465664, 'HP:0002753', 'Thin bony cortex', 'XPO:0102054', 'abnormal notochord morphology', 0.43478260869565216, 4.638757693672553, 1.4201588541997616, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(465665, 'HP:0002753', 'Thin bony cortex', 'XPO:0102514', 'abnormal perichondrial cell morphology', 0.4489795918367347, 6.985637650836012, 1.7709908924643512, 'UPHENO:0002712', 'abnormal connective tissue'),
(465666, 'HP:0002753', 'Thin bony cortex', 'XPO:0128130', 'decreased size of the skeletal tissue', 0.4166666666666667, 6.985637650836012, 1.70607220085054, 'UPHENO:0002712', 'abnormal connective tissue'),
(465667, 'HP:0002753', 'Thin bony cortex', 'XPO:0128091', 'decreased size of the anatomical region', 0.41025641025641024, 5.653868323764771, 1.5230022070142124, 'UPHENO:0012541', 'decreased size of the anatomical entity in the independent continuant'),
(465668, 'HP:0002753', 'Thin bony cortex', 'XPO:0140019', 'abnormally necrotic skeletal system', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(465669, 'HP:0002753', 'Thin bony cortex', 'XPO:0141708', 'decreased size of the posterior notochord', 0.46, 5.653868323764771, 1.6126932222006127, 'UPHENO:0012541', 'decreased size of the anatomical entity in the independent continuant'),
(465670, 'HP:0002753', 'Thin bony cortex', 'XPO:0128246', 'decreased size of the axial skeleton', 0.41818181818181815, 5.653868323764771, 1.5376426552982134, 'UPHENO:0012541', 'decreased size of the anatomical entity in the independent continuant'),
(465671, 'HP:0002753', 'Thin bony cortex', 'XPO:0103355', 'decreased size of the notochord', 0.4423076923076923, 5.653868323764771, 1.5813758095076438, 'UPHENO:0012541', 'decreased size of the anatomical entity in the independent continuant'),
(465672, 'HP:0002753', 'Thin bony cortex', 'XPO:0128037', 'decreased size of the anatomical space', 0.41025641025641024, 5.653868323764771, 1.5230022070142124, 'UPHENO:0012541', 'decreased size of the anatomical entity in the independent continuant'),
(465673, 'HP:0002753', 'Thin bony cortex', 'XPO:0139774', 'abnormally necrotic elastica externa', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(465674, 'HP:0002753', 'Thin bony cortex', 'XPO:0129241', 'decreased size of the bone marrow', 0.40350877192982454, 5.653868323764771, 1.5104255903470578, 'UPHENO:0012541', 'decreased size of the anatomical entity in the independent continuant'),
(465675, 'HP:0002753', 'Thin bony cortex', 'XPO:0115491', 'abnormally increased distribution of connective tissue', 0.4090909090909091, 6.985637650836012, 1.6904913064432443, 'UPHENO:0002712', 'abnormal connective tissue'),
(465676, 'HP:0002753', 'Thin bony cortex', 'XPO:0129664', 'increased size of the skeleton', 0.40384615384615385, 4.6864066944795475, 1.3757133854565902, 'UPHENO:0075195', 'abnormal size of anatomical entity'),
(465677, 'HP:0002753', 'Thin bony cortex', 'XPO:0128220', 'decreased size of the dermal skeleton', 0.42592592592592593, 5.653868323764771, 1.5518147765963477, 'UPHENO:0012541', 'decreased size of the anatomical entity in the independent continuant'),
(465678, 'HP:0002753', 'Thin bony cortex', 'XPO:0128815', 'decreased size of the intersomitic tendon', 0.4032258064516129, 6.985637650836012, 1.67832934054586, 'UPHENO:0002712', 'abnormal connective tissue'),
(465679, 'HP:0025024', 'Megarectum', 'XPO:0101471', 'abnormal rectum', 0.58, 12.7526182249875, 2.719654126997172, 'HP:0002034', 'Abnormal rectum morphology'),
(465680, 'HP:0025024', 'Megarectum', 'XPO:0101288', 'abnormal external coil of the small intestine', 0.46153846153846156, 8.518562886125473, 1.9828374640854927, 'UPHENO:0076783', 'abnormal intestine morphology'),
(465681, 'HP:0025024', 'Megarectum', 'XPO:0101537', 'abnormal internal coil of the small intestine', 0.46153846153846156, 8.518562886125473, 1.9828374640854927, 'UPHENO:0076783', 'abnormal intestine morphology'),
(465682, 'HP:0025024', 'Megarectum', 'XPO:0129430', 'decreased size of the rectum', 0.4393939393939394, 12.7526182249875, 2.3671550771895373, 'HP:0002034', 'Abnormal rectum morphology'),
(465683, 'HP:0025024', 'Megarectum', 'XPO:0100493', 'abnormal liver and biliary system', 0.40540540540540543, 5.05060299610679, 1.4309233924911664, 'HP:0025031', 'Abnormality of the digestive system'),
(465684, 'HP:0025024', 'Megarectum', 'XPO:0115391', 'abnormally undifferentiated alimentary system', 0.40540540540540543, 5.05060299610679, 1.4309233924911664, 'HP:0025031', 'Abnormality of the digestive system'),
(465685, 'HP:0025024', 'Megarectum', 'XPO:0103103', 'abnormal rectum morphology', 0.4915254237288136, 12.7526182249875, 2.50364455877602, 'HP:0002034', 'Abnormal rectum morphology'),
(465686, 'HP:0025024', 'Megarectum', 'XPO:0102788', 'abnormal typhlosole morphology', 0.41379310344827586, 8.518562886125473, 1.8774777158648677, 'UPHENO:0076783', 'abnormal intestine morphology'),
(465687, 'HP:0025024', 'Megarectum', 'XPO:0115392', 'abnormally incomplete structure of alimentary system', 0.4090909090909091, 5.725717590856133, 1.5304701939081158, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(465688, 'HP:0025024', 'Megarectum', 'XPO:0141240', 'abnormally necrotic rectum', 0.453125, 12.7526182249875, 2.4038573446021005, 'HP:0002034', 'Abnormal rectum morphology'),
(465689, 'HP:0025024', 'Megarectum', 'XPO:0102941', 'abnormal colon morphology', 0.4406779661016949, 10.665155383737162, 2.1679250408314017, 'HP:0002250', 'Abnormal large intestine morphology'),
(465690, 'HP:0025024', 'Megarectum', 'XPO:0100361', 'abnormal small intestine', 0.47058823529411764, 8.518562886125473, 2.002182677935196, 'UPHENO:0076783', 'abnormal intestine morphology'),
(465691, 'HP:0025024', 'Megarectum', 'XPO:0107288', 'abnormal larval alimentary system', 0.40540540540540543, 5.05060299610679, 1.4309233924911664, 'HP:0025031', 'Abnormality of the digestive system'),
(465692, 'HP:0025024', 'Megarectum', 'XPO:0140523', 'abnormally necrotic large intestine', 0.41935483870967744, 10.665155383737162, 2.1148249373791543, 'HP:0002250', 'Abnormal large intestine morphology'),
(465693, 'HP:0025024', 'Megarectum', 'XPO:0129624', 'increased size of the large intestine', 0.40625, 10.665155383737162, 2.081518526135, 'HP:0002250', 'Abnormal large intestine morphology'),
(465694, 'HP:0025024', 'Megarectum', 'XPO:0102473', 'abnormal large intestine morphology', 0.45614035087719296, 10.665155383737162, 2.2056309117569177, 'HP:0002250', 'Abnormal large intestine morphology'),
(465695, 'HP:0025024', 'Megarectum', 'XPO:0101784', 'abnormal alimentary system morphology', 0.4186046511627907, 5.725717590856133, 1.5481640787645816, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(465696, 'HP:0025024', 'Megarectum', 'XPO:0102522', 'abnormal pharyngeal cavity morphology', 0.4186046511627907, 5.725717590856133, 1.5481640787645816, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(465697, 'HP:0025024', 'Megarectum', 'XPO:0101321', 'abnormal duodenum', 0.46153846153846156, 8.518562886125473, 1.9828374640854927, 'UPHENO:0076783', 'abnormal intestine morphology'),
(465698, 'HP:0025024', 'Megarectum', 'XPO:0128144', 'decreased size of the large intestine', 0.40625, 10.665155383737162, 2.081518526135, 'HP:0002250', 'Abnormal large intestine morphology'),
(465699, 'HP:0025024', 'Megarectum', 'XPO:0101306', 'abnormal ileum', 0.46153846153846156, 8.518562886125473, 1.9828374640854927, 'UPHENO:0076783', 'abnormal intestine morphology'),
(465700, 'HP:0025024', 'Megarectum', 'XPO:0107294', 'abnormal intestinal stem cell', 0.42857142857142855, 8.518562886125473, 1.9107099898944229, 'UPHENO:0076783', 'abnormal intestine morphology'),
(465701, 'HP:0025024', 'Megarectum', 'XPO:0127034', 'abnormally localised rectum', 0.4915254237288136, 12.7526182249875, 2.50364455877602, 'HP:0002034', 'Abnormal rectum morphology'),
(465702, 'HP:0025024', 'Megarectum', 'XPO:0130904', 'increased size of the rectum', 0.4393939393939394, 12.7526182249875, 2.3671550771895373, 'HP:0002034', 'Abnormal rectum morphology'),
(465703, 'HP:0025024', 'Megarectum', 'XPO:0100152', 'abnormal alimentary system', 0.4166666666666667, 5.05060299610679, 1.45066119926208, 'HP:0025031', 'Abnormality of the digestive system'),
(465704, 'HP:0025024', 'Megarectum', 'XPO:0125399', 'absent rectum', 0.4603174603174603, 12.7526182249875, 2.422860465178382, 'HP:0002034', 'Abnormal rectum morphology'),
(465705, 'HP:0025241', 'Flame-shaped retinal hemorrhage', 'XPO:0128330', 'decreased size of the retinal progenitor cell region', 0.4479166666666667, 8.040873045973026, 1.8977990019604511, 'HP:0000479', 'Abnormal retinal morphology'),
(465706, 'HP:0025241', 'Flame-shaped retinal hemorrhage', 'XPO:0140487', 'abnormally necrotic retinal layer', 0.4725274725274725, 8.040873045973026, 1.9492391893577128, 'HP:0000479', 'Abnormal retinal morphology'),
(465707, 'HP:0025241', 'Flame-shaped retinal hemorrhage', 'XPO:0102017', 'abnormal retinal neural layer morphology', 0.43, 8.040873045973026, 1.859455675666511, 'HP:0000479', 'Abnormal retinal morphology'),
(465708, 'HP:0025241', 'Flame-shaped retinal hemorrhage', 'XPO:0102784', 'abnormal retinal progenitor cell region morphology', 0.4725274725274725, 8.040873045973026, 1.9492391893577128, 'HP:0000479', 'Abnormal retinal morphology'),
(465709, 'HP:0025241', 'Flame-shaped retinal hemorrhage', 'XPO:0102946', 'abnormal retinal inner nuclear layer morphology', 0.42574257425742573, 8.040873045973026, 1.850227550835222, 'HP:0000479', 'Abnormal retinal morphology'),
(465710, 'HP:0025241', 'Flame-shaped retinal hemorrhage', 'XPO:0102232', 'abnormal eye photoreceptor cell morphology', 0.41346153846153844, 8.040873045973026, 1.8233463028623837, 'HP:0000479', 'Abnormal retinal morphology'),
(465711, 'HP:0025241', 'Flame-shaped retinal hemorrhage', 'XPO:0125909', 'absent retinal blood vessel', 0.45454545454545453, 8.040873045973026, 1.911790337255658, 'HP:0000479', 'Abnormal retinal morphology'),
(465712, 'HP:0025241', 'Flame-shaped retinal hemorrhage', 'XPO:0102162', 'abnormal ciliary marginal zone morphology', 0.45263157894736844, 8.040873045973026, 1.9077612698957138, 'HP:0000479', 'Abnormal retinal morphology'),
(465713, 'HP:0025241', 'Flame-shaped retinal hemorrhage', 'XPO:0130148', 'increased size of the ciliary marginal zone', 0.4095238095238095, 8.040873045973026, 1.8146429295275122, 'HP:0000479', 'Abnormal retinal morphology'),
(465714, 'HP:0025241', 'Flame-shaped retinal hemorrhage', 'XPO:0102505', 'abnormal retinal stem cell region morphology', 0.4725274725274725, 8.040873045973026, 1.9492391893577128, 'HP:0000479', 'Abnormal retinal morphology'),
(465715, 'HP:0025241', 'Flame-shaped retinal hemorrhage', 'XPO:0101861', 'abnormal photoreceptor layer morphology', 0.43, 8.040873045973026, 1.859455675666511, 'HP:0000479', 'Abnormal retinal morphology'),
(465716, 'HP:0025241', 'Flame-shaped retinal hemorrhage', 'XPO:0102756', 'abnormal Muller cell morphology', 0.45263157894736844, 8.040873045973026, 1.9077612698957138, 'HP:0000479', 'Abnormal retinal morphology'),
(465717, 'HP:0025241', 'Flame-shaped retinal hemorrhage', 'XPO:0140439', 'abnormally necrotic retinal stem cell', 0.4095238095238095, 8.040873045973026, 1.8146429295275122, 'HP:0000479', 'Abnormal retinal morphology'),
(465718, 'HP:0025241', 'Flame-shaped retinal hemorrhage', 'XPO:0128300', 'decreased size of the retina', 0.4574468085106383, 8.040873045973026, 1.9178820903589395, 'HP:0000479', 'Abnormal retinal morphology'),
(465719, 'HP:0025241', 'Flame-shaped retinal hemorrhage', 'XPO:0140391', 'abnormally necrotic central retina', 0.4777777777777778, 8.040873045973026, 1.960038381077836, 'HP:0000479', 'Abnormal retinal morphology'),
(465720, 'HP:0025241', 'Flame-shaped retinal hemorrhage', 'XPO:0103226', 'abnormal retinal outer plexiform layer morphology', 0.42574257425742573, 8.040873045973026, 1.850227550835222, 'HP:0000479', 'Abnormal retinal morphology'),
(465721, 'HP:0025241', 'Flame-shaped retinal hemorrhage', 'XPO:0140346', 'abnormally necrotic retinal blood vessel', 0.41284403669724773, 8.040873045973026, 1.8219842169650093, 'HP:0000479', 'Abnormal retinal morphology'),
(465722, 'HP:0025241', 'Flame-shaped retinal hemorrhage', 'XPO:0102818', 'abnormal optic chiasm morphology', 0.41, 7.796308075334707, 1.7878720062933, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(465723, 'HP:0025241', 'Flame-shaped retinal hemorrhage', 'XPO:0128935', 'decreased size of the central retina', 0.4673913043478261, 8.040873045973026, 1.938616553383523, 'HP:0000479', 'Abnormal retinal morphology'),
(465724, 'HP:0025241', 'Flame-shaped retinal hemorrhage', 'XPO:0129955', 'increased size of the retinal stem cell region', 0.4479166666666667, 8.040873045973026, 1.8977990019604511, 'HP:0000479', 'Abnormal retinal morphology'),
(465725, 'HP:0025241', 'Flame-shaped retinal hemorrhage', 'XPO:0100329', 'abnormal retinal blood vessel', 0.5357142857142857, 8.040873045973026, 2.075478393128363, 'HP:0000479', 'Abnormal retinal morphology'),
(465726, 'HP:0025241', 'Flame-shaped retinal hemorrhage', 'XPO:0128643', 'decreased size of the retinal layer', 0.4673913043478261, 8.040873045973026, 1.938616553383523, 'HP:0000479', 'Abnormal retinal morphology'),
(465727, 'HP:0025241', 'Flame-shaped retinal hemorrhage', 'XPO:0102239', 'abnormal retinal pigmented epithelium morphology', 0.42574257425742573, 8.040873045973026, 1.850227550835222, 'HP:0000479', 'Abnormal retinal morphology'),
(465728, 'HP:0025241', 'Flame-shaped retinal hemorrhage', 'XPO:0141033', 'abnormally necrotic photoreceptor layer', 0.40186915887850466, 8.040873045973026, 1.797603651429875, 'HP:0000479', 'Abnormal retinal morphology'),
(465729, 'HP:0025241', 'Flame-shaped retinal hemorrhage', 'XPO:0130122', 'increased size of the retinal layer', 0.4673913043478261, 8.040873045973026, 1.938616553383523, 'HP:0000479', 'Abnormal retinal morphology'),
(465730, 'HP:0025241', 'Flame-shaped retinal hemorrhage', 'XPO:0129780', 'increased size of the retina', 0.4574468085106383, 8.040873045973026, 1.9178820903589395, 'HP:0000479', 'Abnormal retinal morphology'),
(465731, 'HP:0025241', 'Flame-shaped retinal hemorrhage', 'XPO:0141333', 'increased pigmentation in the retinal pigmented epithelium', 0.41346153846153844, 8.040873045973026, 1.8233463028623837, 'HP:0000479', 'Abnormal retinal morphology'),
(465732, 'HP:0025241', 'Flame-shaped retinal hemorrhage', 'XPO:0103186', 'abnormal peripheral retina morphology', 0.4777777777777778, 8.040873045973026, 1.960038381077836, 'HP:0000479', 'Abnormal retinal morphology'),
(465733, 'HP:0025241', 'Flame-shaped retinal hemorrhage', 'XPO:0102939', 'abnormal retinal ganglion cell layer morphology', 0.42574257425742573, 8.040873045973026, 1.850227550835222, 'HP:0000479', 'Abnormal retinal morphology'),
(465734, 'HP:0025241', 'Flame-shaped retinal hemorrhage', 'XPO:0102266', 'abnormal horizontal cell morphology', 0.4095238095238095, 8.040873045973026, 1.8146429295275122, 'HP:0000479', 'Abnormal retinal morphology'),
(465735, 'HP:0025241', 'Flame-shaped retinal hemorrhage', 'XPO:0102441', 'abnormal retinal inner plexiform layer morphology', 0.42574257425742573, 8.040873045973026, 1.850227550835222, 'HP:0000479', 'Abnormal retinal morphology'),
(465736, 'HP:0025241', 'Flame-shaped retinal hemorrhage', 'XPO:0139887', 'abnormally necrotic Muller cell', 0.43, 8.040873045973026, 1.859455675666511, 'HP:0000479', 'Abnormal retinal morphology'),
(465737, 'HP:0025241', 'Flame-shaped retinal hemorrhage', 'XPO:0100371', 'abnormal hyaloid blood vessel', 0.4024390243902439, 6.887869297006056, 1.6649166345540045, 'HP:0012372', 'Abnormal eye morphology'),
(465738, 'HP:0025241', 'Flame-shaped retinal hemorrhage', 'XPO:0102996', 'abnormal optic fiber layer morphology', 0.42574257425742573, 8.040873045973026, 1.850227550835222, 'HP:0000479', 'Abnormal retinal morphology'),
(465739, 'HP:0025241', 'Flame-shaped retinal hemorrhage', 'XPO:0140553', 'abnormally necrotic retinal stem cell region', 0.4574468085106383, 8.040873045973026, 1.9178820903589395, 'HP:0000479', 'Abnormal retinal morphology'),
(465740, 'HP:0025241', 'Flame-shaped retinal hemorrhage', 'XPO:0140531', 'abnormally necrotic retinal progenitor cell region', 0.4574468085106383, 8.040873045973026, 1.9178820903589395, 'HP:0000479', 'Abnormal retinal morphology'),
(465741, 'HP:0025241', 'Flame-shaped retinal hemorrhage', 'XPO:0127563', 'abnormally localised retinal blood vessel', 0.4787234042553192, 8.040873045973026, 1.961977094094894, 'HP:0000479', 'Abnormal retinal morphology'),
(465742, 'HP:0025241', 'Flame-shaped retinal hemorrhage', 'XPO:0130257', 'increased size of the retinal blood vessel', 0.40540540540540543, 8.040873045973026, 1.8054953328702048, 'HP:0000479', 'Abnormal retinal morphology'),
(465743, 'HP:0025241', 'Flame-shaped retinal hemorrhage', 'XPO:0102851', 'abnormal retinal rod cell morphology', 0.4056603773584906, 8.040873045973026, 1.8060630094548564, 'HP:0000479', 'Abnormal retinal morphology'),
(465744, 'HP:0025241', 'Flame-shaped retinal hemorrhage', 'XPO:0103926', 'decreased pigmentation in the retinal pigmented epithelium', 0.41346153846153844, 8.040873045973026, 1.8233463028623837, 'HP:0000479', 'Abnormal retinal morphology'),
(465745, 'HP:0025241', 'Flame-shaped retinal hemorrhage', 'XPO:0102805', 'abnormal retinal layer morphology', 0.5058823529411764, 8.040873045973026, 2.0168628550791743, 'HP:0000479', 'Abnormal retinal morphology'),
(465746, 'HP:0025241', 'Flame-shaped retinal hemorrhage', 'XPO:0128787', 'decreased size of the peripheral retina', 0.4387755102040816, 8.040873045973026, 1.8783338822565765, 'HP:0000479', 'Abnormal retinal morphology'),
(465747, 'HP:0025241', 'Flame-shaped retinal hemorrhage', 'XPO:0130265', 'increased size of the peripheral retina', 0.4387755102040816, 8.040873045973026, 1.8783338822565765, 'HP:0000479', 'Abnormal retinal morphology'),
(465748, 'HP:0025241', 'Flame-shaped retinal hemorrhage', 'XPO:0140271', 'abnormally necrotic peripheral retina', 0.4479166666666667, 8.040873045973026, 1.8977990019604511, 'HP:0000479', 'Abnormal retinal morphology'),
(465749, 'HP:0025241', 'Flame-shaped retinal hemorrhage', 'XPO:0128779', 'decreased size of the retinal blood vessel', 0.40540540540540543, 8.040873045973026, 1.8054953328702048, 'HP:0000479', 'Abnormal retinal morphology'),
(465750, 'HP:0025241', 'Flame-shaped retinal hemorrhage', 'XPO:0102117', 'abnormal retina morphology', 0.4942528735632184, 8.040873045973026, 1.9935457378573478, 'HP:0000479', 'Abnormal retinal morphology'),
(465751, 'HP:0025241', 'Flame-shaped retinal hemorrhage', 'XPO:0103184', 'abnormal inner limiting membrane morphology', 0.42574257425742573, 8.040873045973026, 1.850227550835222, 'HP:0000479', 'Abnormal retinal morphology'),
(465752, 'HP:0025241', 'Flame-shaped retinal hemorrhage', 'XPO:0102663', 'abnormal retinal progenitor cell morphology', 0.43, 8.040873045973026, 1.859455675666511, 'HP:0000479', 'Abnormal retinal morphology'),
(465753, 'HP:0025241', 'Flame-shaped retinal hemorrhage', 'XPO:0102815', 'abnormal retinal ganglion cell morphology', 0.40186915887850466, 8.040873045973026, 1.797603651429875, 'HP:0000479', 'Abnormal retinal morphology'),
(465754, 'HP:0025241', 'Flame-shaped retinal hemorrhage', 'XPO:0140489', 'abnormally necrotic ciliary marginal zone', 0.4174757281553398, 8.040873045973026, 1.8321761186829812, 'HP:0000479', 'Abnormal retinal morphology'),
(465755, 'HP:0025241', 'Flame-shaped retinal hemorrhage', 'XPO:0128475', 'decreased size of the retinal stem cell region', 0.4479166666666667, 8.040873045973026, 1.8977990019604511, 'HP:0000479', 'Abnormal retinal morphology'),
(465756, 'HP:0025241', 'Flame-shaped retinal hemorrhage', 'XPO:0140192', 'abnormally necrotic retina', 0.4673913043478261, 8.040873045973026, 1.938616553383523, 'HP:0000479', 'Abnormal retinal morphology'),
(465757, 'HP:0025241', 'Flame-shaped retinal hemorrhage', 'XPO:0101961', 'abnormal retinal blood vessel morphology', 0.4411764705882353, 8.040873045973026, 1.8834659516090149, 'HP:0000479', 'Abnormal retinal morphology'),
(465758, 'HP:0025241', 'Flame-shaped retinal hemorrhage', 'XPO:0129810', 'increased size of the retinal progenitor cell region', 0.4479166666666667, 8.040873045973026, 1.8977990019604511, 'HP:0000479', 'Abnormal retinal morphology'),
(465759, 'HP:0025241', 'Flame-shaped retinal hemorrhage', 'XPO:0140317', 'abnormally necrotic retinal progenitor cell', 0.4095238095238095, 8.040873045973026, 1.8146429295275122, 'HP:0000479', 'Abnormal retinal morphology'),
(465760, 'HP:0025241', 'Flame-shaped retinal hemorrhage', 'XPO:0102963', 'abnormal retinal outer nuclear layer morphology', 0.42574257425742573, 8.040873045973026, 1.850227550835222, 'HP:0000479', 'Abnormal retinal morphology'),
(465761, 'HP:0025241', 'Flame-shaped retinal hemorrhage', 'XPO:0102450', 'abnormal retinal stem cell morphology', 0.43, 8.040873045973026, 1.859455675666511, 'HP:0000479', 'Abnormal retinal morphology'),
(465762, 'HP:0025241', 'Flame-shaped retinal hemorrhage', 'XPO:0102581', 'abnormal outer limiting membrane morphology', 0.42574257425742573, 8.040873045973026, 1.850227550835222, 'HP:0000479', 'Abnormal retinal morphology'),
(465763, 'HP:0025241', 'Flame-shaped retinal hemorrhage', 'XPO:0102196', 'abnormal central retina morphology', 0.4942528735632184, 8.040873045973026, 1.9935457378573478, 'HP:0000479', 'Abnormal retinal morphology'),
(465764, 'HP:0025241', 'Flame-shaped retinal hemorrhage', 'XPO:0128669', 'decreased size of the ciliary marginal zone', 0.4095238095238095, 8.040873045973026, 1.8146429295275122, 'HP:0000479', 'Abnormal retinal morphology'),
(465765, 'HP:0025241', 'Flame-shaped retinal hemorrhage', 'XPO:0130413', 'increased size of the central retina', 0.4673913043478261, 8.040873045973026, 1.938616553383523, 'HP:0000479', 'Abnormal retinal morphology'),
(465766, 'HP:0025241', 'Flame-shaped retinal hemorrhage', 'XPO:0102882', 'abnormal retinal cone cell morphology', 0.4056603773584906, 8.040873045973026, 1.8060630094548564, 'HP:0000479', 'Abnormal retinal morphology'),
(465767, 'HP:0032090', 'Intralamellar aortic medial fibrosis', 'XPO:0141223', 'abnormally necrotic Jacobsons vein', 0.4032258064516129, 7.803720102857406, 1.7738831223610367, 'HP:0033353', 'Abnormal blood vessel morphology'),
(465768, 'HP:0032090', 'Intralamellar aortic medial fibrosis', 'XPO:0102154', 'abnormal subinterstitial vein morphology', 0.45454545454545453, 7.803720102857406, 1.8833867105028699, 'HP:0033353', 'Abnormal blood vessel morphology'),
(465769, 'HP:0032090', 'Intralamellar aortic medial fibrosis', 'XPO:0129572', 'increased size of the paired dorsal aorta', 0.4626865671641791, 9.604719529875187, 2.1080736960203024, 'UPHENO:0076809', 'abnormal aorta morphology'),
(465770, 'HP:0032090', 'Intralamellar aortic medial fibrosis', 'XPO:0102683', 'abnormal intersomitic vein morphology', 0.42857142857142855, 6.974839882869777, 1.7289352482549702, 'UPHENO:0087186', 'abnormal blood vessel morphology'),
(465771, 'HP:0032090', 'Intralamellar aortic medial fibrosis', 'XPO:0101995', 'abnormal cardiovascular system morphology', 0.4222222222222222, 5.9590888072311134, 1.5862092291399303, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(465772, 'HP:0032090', 'Intralamellar aortic medial fibrosis', 'XPO:0103091', 'abnormal arteria iliaca communis morphology', 0.421875, 8.750570396338642, 1.921365890702592, 'HP:0011004', 'Abnormal systemic arterial morphology'),
(465773, 'HP:0032090', 'Intralamellar aortic medial fibrosis', 'XPO:0130014', 'increased size of the vascular plexus', 0.4067796610169492, 6.974839882869777, 1.6844058309093048, 'UPHENO:0087186', 'abnormal blood vessel morphology'),
(465774, 'HP:0032090', 'Intralamellar aortic medial fibrosis', 'XPO:0102291', 'abnormal anterior cardinal vein morphology', 0.4166666666666667, 7.803720102857406, 1.8032054910234865, 'HP:0033353', 'Abnormal blood vessel morphology'),
(465775, 'HP:0032090', 'Intralamellar aortic medial fibrosis', 'XPO:0141029', 'abnormally necrotic subinterstitial vein', 0.4032258064516129, 7.803720102857406, 1.7738831223610367, 'HP:0033353', 'Abnormal blood vessel morphology'),
(465776, 'HP:0032090', 'Intralamellar aortic medial fibrosis', 'XPO:0103063', 'abnormal ischiadic artery morphology', 0.4444444444444444, 6.974839882869777, 1.7606614770679263, 'UPHENO:0087186', 'abnormal blood vessel morphology'),
(465777, 'HP:0032090', 'Intralamellar aortic medial fibrosis', 'XPO:0141260', 'abnormally necrotic dorsal longitudinal anastomosing vessel - left branch', 0.4067796610169492, 6.974839882869777, 1.6844058309093048, 'UPHENO:0087186', 'abnormal blood vessel morphology'),
(465778, 'HP:0032090', 'Intralamellar aortic medial fibrosis', 'XPO:0102612', 'abnormal dorsal longitudinal anastomosing vessel - left branch morphology', 0.46153846153846156, 6.974839882869777, 1.7942008998484034, 'UPHENO:0087186', 'abnormal blood vessel morphology'),
(465779, 'HP:0032090', 'Intralamellar aortic medial fibrosis', 'XPO:0130150', 'increased size of the capillary', 0.4098360655737705, 7.803720102857406, 1.788364041182337, 'HP:0033353', 'Abnormal blood vessel morphology'),
(465780, 'HP:0032090', 'Intralamellar aortic medial fibrosis', 'XPO:0102251', 'abnormal interrenal vein morphology', 0.4166666666666667, 7.803720102857406, 1.8032054910234865, 'HP:0033353', 'Abnormal blood vessel morphology'),
(465781, 'HP:0032090', 'Intralamellar aortic medial fibrosis', 'XPO:0139723', 'abnormally necrotic blood vessel', 0.4528301886792453, 6.974839882869777, 1.7771938724200707, 'UPHENO:0087186', 'abnormal blood vessel morphology'),
(465782, 'HP:0032090', 'Intralamellar aortic medial fibrosis', 'XPO:0101675', 'abnormal vein morphology', 0.4716981132075472, 7.803720102857406, 1.9185932472824052, 'HP:0033353', 'Abnormal blood vessel morphology'),
(465783, 'HP:0032090', 'Intralamellar aortic medial fibrosis', 'XPO:0140207', 'abnormally necrotic branchial vein', 0.4032258064516129, 7.803720102857406, 1.7738831223610367, 'HP:0033353', 'Abnormal blood vessel morphology'),
(465784, 'HP:0032090', 'Intralamellar aortic medial fibrosis', 'XPO:0102619', 'abnormal larval aorta morphology', 0.4444444444444444, 6.974839882869777, 1.7606614770679263, 'UPHENO:0087186', 'abnormal blood vessel morphology'),
(465785, 'HP:0032090', 'Intralamellar aortic medial fibrosis', 'XPO:0103119', 'abnormal epigastric artery morphology', 0.4067796610169492, 6.974839882869777, 1.6844058309093048, 'UPHENO:0087186', 'abnormal blood vessel morphology'),
(465786, 'HP:0032090', 'Intralamellar aortic medial fibrosis', 'XPO:0141079', 'abnormally necrotic ischiadic vein', 0.4032258064516129, 7.803720102857406, 1.7738831223610367, 'HP:0033353', 'Abnormal blood vessel morphology'),
(465787, 'HP:0032090', 'Intralamellar aortic medial fibrosis', 'XPO:0128147', 'decreased size of the ventral aorta', 0.4305555555555556, 9.604719529875187, 2.0335597736827666, 'UPHENO:0076809', 'abnormal aorta morphology'),
(465788, 'HP:0032090', 'Intralamellar aortic medial fibrosis', 'XPO:0102962', 'abnormal postcaval vein morphology', 0.4166666666666667, 7.803720102857406, 1.8032054910234865, 'HP:0033353', 'Abnormal blood vessel morphology'),
(465789, 'HP:0032090', 'Intralamellar aortic medial fibrosis', 'XPO:0128028', 'decreased size of the vein', 0.4098360655737705, 7.803720102857406, 1.788364041182337, 'HP:0033353', 'Abnormal blood vessel morphology'),
(465790, 'HP:0032090', 'Intralamellar aortic medial fibrosis', 'XPO:0102838', 'abnormal ischiadic vein morphology', 0.45454545454545453, 7.803720102857406, 1.8833867105028699, 'HP:0033353', 'Abnormal blood vessel morphology'),
(465791, 'HP:0032090', 'Intralamellar aortic medial fibrosis', 'XPO:0130400', 'increased size of the dorsal longitudinal anastomosing vessel', 0.41379310344827586, 6.974839882869777, 1.6988645152534954, 'UPHENO:0087186', 'abnormal blood vessel morphology'),
(465792, 'HP:0032090', 'Intralamellar aortic medial fibrosis', 'XPO:0101956', 'abnormal intersomitic vessel morphology', 0.4444444444444444, 6.974839882869777, 1.7606614770679263, 'UPHENO:0087186', 'abnormal blood vessel morphology'),
(465793, 'HP:0032090', 'Intralamellar aortic medial fibrosis', 'XPO:0128671', 'decreased size of the capillary', 0.4098360655737705, 7.803720102857406, 1.788364041182337, 'HP:0033353', 'Abnormal blood vessel morphology'),
(465794, 'HP:0032090', 'Intralamellar aortic medial fibrosis', 'XPO:0141134', 'abnormally necrotic caudal artery', 0.45588235294117646, 9.604719529875187, 2.09251574393589, 'UPHENO:0076809', 'abnormal aorta morphology'),
(465795, 'HP:0032090', 'Intralamellar aortic medial fibrosis', 'XPO:0102355', 'abnormal lateral postcardinal vein morphology', 0.4166666666666667, 7.803720102857406, 1.8032054910234865, 'HP:0033353', 'Abnormal blood vessel morphology'),
(465796, 'HP:0032090', 'Intralamellar aortic medial fibrosis', 'XPO:0128364', 'decreased size of the dorsal aorta', 0.4305555555555556, 9.604719529875187, 2.0335597736827666, 'UPHENO:0076809', 'abnormal aorta morphology'),
(465797, 'HP:0032090', 'Intralamellar aortic medial fibrosis', 'XPO:0102993', 'abnormal musculoabdominal vein morphology', 0.4166666666666667, 7.803720102857406, 1.8032054910234865, 'HP:0033353', 'Abnormal blood vessel morphology'),
(465798, 'HP:0032090', 'Intralamellar aortic medial fibrosis', 'XPO:0128534', 'decreased size of the vascular plexus', 0.4067796610169492, 6.974839882869777, 1.6844058309093048, 'UPHENO:0087186', 'abnormal blood vessel morphology'),
(465799, 'HP:0032090', 'Intralamellar aortic medial fibrosis', 'XPO:0130772', 'increased size of the truncus arteriosus', 0.41379310344827586, 6.974839882869777, 1.6988645152534954, 'UPHENO:0087186', 'abnormal blood vessel morphology'),
(465800, 'HP:0032090', 'Intralamellar aortic medial fibrosis', 'XPO:0101900', 'abnormal circulatory system morphology', 0.4222222222222222, 5.9590888072311134, 1.5862092291399303, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(465801, 'HP:0032090', 'Intralamellar aortic medial fibrosis', 'XPO:0129344', 'decreased size of the caudal artery', 0.44285714285714284, 9.604719529875187, 2.0624060339672994, 'UPHENO:0076809', 'abnormal aorta morphology'),
(465802, 'HP:0032090', 'Intralamellar aortic medial fibrosis', 'XPO:0130660', 'increased size of the arteria mesenterica posterior', 0.43661971830985913, 9.604719529875187, 2.047830543667934, 'UPHENO:0076809', 'abnormal aorta morphology'),
(465803, 'HP:0032090', 'Intralamellar aortic medial fibrosis', 'XPO:0129844', 'increased size of the dorsal aorta', 0.4305555555555556, 9.604719529875187, 2.0335597736827666, 'UPHENO:0076809', 'abnormal aorta morphology'),
(465804, 'HP:0032090', 'Intralamellar aortic medial fibrosis', 'XPO:0101708', 'abnormal artery morphology', 0.46153846153846156, 6.974839882869777, 1.7942008998484034, 'UPHENO:0087186', 'abnormal blood vessel morphology'),
(465805, 'HP:0032090', 'Intralamellar aortic medial fibrosis', 'XPO:0101845', 'abnormal right channel of ventral aorta morphology', 0.4067796610169492, 6.974839882869777, 1.6844058309093048, 'UPHENO:0087186', 'abnormal blood vessel morphology'),
(465806, 'HP:0032090', 'Intralamellar aortic medial fibrosis', 'XPO:0141249', 'abnormally necrotic dorsal longitudinal anastomosing vessel - right branch', 0.4067796610169492, 6.974839882869777, 1.6844058309093048, 'UPHENO:0087186', 'abnormal blood vessel morphology'),
(465807, 'HP:0032090', 'Intralamellar aortic medial fibrosis', 'XPO:0129573', 'increased size of the aorta', 0.484375, 9.604719529875187, 2.156915858878898, 'UPHENO:0076809', 'abnormal aorta morphology'),
(465808, 'HP:0032090', 'Intralamellar aortic medial fibrosis', 'XPO:0140152', 'abnormally necrotic capillary', 0.423728813559322, 7.803720102857406, 1.818422684782831, 'HP:0033353', 'Abnormal blood vessel morphology'),
(465809, 'HP:0032090', 'Intralamellar aortic medial fibrosis', 'XPO:0101154', 'abnormal external carotid artery', 0.4426229508196721, 8.750570396338642, 1.9680455508403958, 'HP:0011004', 'Abnormal systemic arterial morphology'),
(465810, 'HP:0032090', 'Intralamellar aortic medial fibrosis', 'XPO:0140595', 'abnormally necrotic dorsal longitudinal anastomosing vessel', 0.42857142857142855, 6.974839882869777, 1.7289352482549702, 'UPHENO:0087186', 'abnormal blood vessel morphology'),
(465811, 'HP:0032090', 'Intralamellar aortic medial fibrosis', 'XPO:0102904', 'abnormal lateral abdominal vein morphology', 0.4166666666666667, 7.803720102857406, 1.8032054910234865, 'HP:0033353', 'Abnormal blood vessel morphology'),
(465812, 'HP:0032090', 'Intralamellar aortic medial fibrosis', 'XPO:0103217', 'abnormal dorsal longitudinal anastomosing vessel - right branch morphology', 0.46153846153846156, 6.974839882869777, 1.7942008998484034, 'UPHENO:0087186', 'abnormal blood vessel morphology'),
(465813, 'HP:0032090', 'Intralamellar aortic medial fibrosis', 'XPO:0102284', 'abnormal medial cardinal vein morphology', 0.4166666666666667, 7.803720102857406, 1.8032054910234865, 'HP:0033353', 'Abnormal blood vessel morphology'),
(465814, 'HP:0032090', 'Intralamellar aortic medial fibrosis', 'XPO:0103189', 'abnormal Jacobsons vein morphology', 0.45454545454545453, 7.803720102857406, 1.8833867105028699, 'HP:0033353', 'Abnormal blood vessel morphology'),
(465815, 'HP:0032090', 'Intralamellar aortic medial fibrosis', 'XPO:0102412', 'abnormal vascular plexus morphology', 0.47058823529411764, 6.974839882869777, 1.8117057133924146, 'UPHENO:0087186', 'abnormal blood vessel morphology'),
(465816, 'HP:0032090', 'Intralamellar aortic medial fibrosis', 'XPO:0102709', 'abnormal ventral abdominal vein morphology', 0.4166666666666667, 7.803720102857406, 1.8032054910234865, 'HP:0033353', 'Abnormal blood vessel morphology'),
(465817, 'HP:0032090', 'Intralamellar aortic medial fibrosis', 'XPO:0129184', 'decreased size of the arteria mesenterica posterior', 0.43661971830985913, 9.604719529875187, 2.047830543667934, 'UPHENO:0076809', 'abnormal aorta morphology'),
(465818, 'HP:0032090', 'Intralamellar aortic medial fibrosis', 'XPO:0139828', 'abnormally necrotic paired dorsal aorta', 0.47692307692307695, 9.604719529875187, 2.1402598886983895, 'UPHENO:0076809', 'abnormal aorta morphology'),
(465819, 'HP:0032090', 'Intralamellar aortic medial fibrosis', 'XPO:0103157', 'abnormal posterior vena cava morphology', 0.4090909090909091, 9.164925931510773, 1.9363077960573802, 'UPHENO:0076765', 'abnormal great vessel of heart morphology'),
(465820, 'HP:0032090', 'Intralamellar aortic medial fibrosis', 'XPO:0140850', 'abnormally necrotic arteria mesenterica posterior', 0.4492753623188406, 9.604719529875187, 2.0772972456428853, 'UPHENO:0076809', 'abnormal aorta morphology'),
(465821, 'HP:0032090', 'Intralamellar aortic medial fibrosis', 'XPO:0128922', 'decreased size of the dorsal longitudinal anastomosing vessel', 0.41379310344827586, 6.974839882869777, 1.6988645152534954, 'UPHENO:0087186', 'abnormal blood vessel morphology'),
(465822, 'HP:0032090', 'Intralamellar aortic medial fibrosis', 'XPO:0129510', 'increased size of the blood vessel', 0.43636363636363634, 6.974839882869777, 1.744582040015079, 'UPHENO:0087186', 'abnormal blood vessel morphology'),
(465823, 'HP:0032090', 'Intralamellar aortic medial fibrosis', 'XPO:0128030', 'decreased size of the blood vessel', 0.43636363636363634, 6.974839882869777, 1.744582040015079, 'UPHENO:0087186', 'abnormal blood vessel morphology'),
(465824, 'HP:0032090', 'Intralamellar aortic medial fibrosis', 'XPO:0101916', 'abnormal tail vasculature morphology', 0.42857142857142855, 6.974839882869777, 1.7289352482549702, 'UPHENO:0087186', 'abnormal blood vessel morphology'),
(465825, 'HP:0032090', 'Intralamellar aortic medial fibrosis', 'XPO:0101769', 'abnormal cardinal vein morphology', 0.43859649122807015, 7.803720102857406, 1.8500497981511776, 'HP:0033353', 'Abnormal blood vessel morphology'),
(465826, 'HP:0032090', 'Intralamellar aortic medial fibrosis', 'XPO:0101780', 'abnormal arteria mesenterica posterior morphology', 0.5, 9.604719529875187, 2.19142870405076, 'UPHENO:0076809', 'abnormal aorta morphology'),
(465827, 'HP:0032090', 'Intralamellar aortic medial fibrosis', 'XPO:0129296', 'decreased size of the truncus arteriosus', 0.41379310344827586, 6.974839882869777, 1.6988645152534954, 'UPHENO:0087186', 'abnormal blood vessel morphology'),
(465828, 'HP:0032090', 'Intralamellar aortic medial fibrosis', 'XPO:0102311', 'abnormal left channel of ventral aorta morphology', 0.4067796610169492, 6.974839882869777, 1.6844058309093048, 'UPHENO:0087186', 'abnormal blood vessel morphology'),
(465829, 'HP:0032090', 'Intralamellar aortic medial fibrosis', 'XPO:0128093', 'decreased size of the aorta', 0.484375, 9.604719529875187, 2.156915858878898, 'UPHENO:0076809', 'abnormal aorta morphology'),
(465830, 'HP:0032090', 'Intralamellar aortic medial fibrosis', 'XPO:0102166', 'abnormal medial abdominal vein morphology', 0.4166666666666667, 7.803720102857406, 1.8032054910234865, 'HP:0033353', 'Abnormal blood vessel morphology'),
(465831, 'HP:0032090', 'Intralamellar aortic medial fibrosis', 'XPO:0128092', 'decreased size of the paired dorsal aorta', 0.4626865671641791, 9.604719529875187, 2.1080736960203024, 'UPHENO:0076809', 'abnormal aorta morphology'),
(465832, 'HP:0032090', 'Intralamellar aortic medial fibrosis', 'XPO:0101711', 'abnormal dorsal aorta morphology', 0.5, 9.604719529875187, 2.19142870405076, 'UPHENO:0076809', 'abnormal aorta morphology'),
(465833, 'HP:0032090', 'Intralamellar aortic medial fibrosis', 'XPO:0103215', 'abnormal truncus arteriosus morphology', 0.48, 6.974839882869777, 1.8297330799265483, 'UPHENO:0087186', 'abnormal blood vessel morphology'),
(465834, 'HP:0032090', 'Intralamellar aortic medial fibrosis', 'XPO:0129508', 'increased size of the vein', 0.4098360655737705, 7.803720102857406, 1.788364041182337, 'HP:0033353', 'Abnormal blood vessel morphology'),
(465835, 'HP:0032090', 'Intralamellar aortic medial fibrosis', 'XPO:0102565', 'abnormal branchial vein morphology', 0.45454545454545453, 7.803720102857406, 1.8833867105028699, 'HP:0033353', 'Abnormal blood vessel morphology'),
(465836, 'HP:0032090', 'Intralamellar aortic medial fibrosis', 'XPO:0140755', 'abnormally necrotic vascular plexus', 0.42105263157894735, 6.974839882869777, 1.7137020416408788, 'UPHENO:0087186', 'abnormal blood vessel morphology'),
(465837, 'HP:0032090', 'Intralamellar aortic medial fibrosis', 'XPO:0102421', 'abnormal occipitovertebral artery morphology', 0.4444444444444444, 6.974839882869777, 1.7606614770679263, 'UPHENO:0087186', 'abnormal blood vessel morphology'),
(465838, 'HP:0032090', 'Intralamellar aortic medial fibrosis', 'XPO:0139803', 'abnormally necrotic aorta', 0.5, 9.604719529875187, 2.19142870405076, 'UPHENO:0076809', 'abnormal aorta morphology'),
(465839, 'HP:0032090', 'Intralamellar aortic medial fibrosis', 'XPO:0101686', 'abnormal blood vessel morphology', 0.5, 6.974839882869777, 1.8674635047129806, 'UPHENO:0087186', 'abnormal blood vessel morphology'),
(465840, 'HP:0032090', 'Intralamellar aortic medial fibrosis', 'XPO:0102849', 'abnormal tail vein morphology', 0.4098360655737705, 7.803720102857406, 1.788364041182337, 'HP:0033353', 'Abnormal blood vessel morphology'),
(465841, 'HP:0032090', 'Intralamellar aortic medial fibrosis', 'XPO:0102424', 'abnormal capillary morphology', 0.4716981132075472, 7.803720102857406, 1.9185932472824052, 'HP:0033353', 'Abnormal blood vessel morphology'),
(465842, 'HP:0032090', 'Intralamellar aortic medial fibrosis', 'XPO:0102748', 'abnormal lateral vein morphology', 0.4166666666666667, 7.803720102857406, 1.8032054910234865, 'HP:0033353', 'Abnormal blood vessel morphology'),
(465843, 'HP:0032090', 'Intralamellar aortic medial fibrosis', 'XPO:0101829', 'abnormal subclavian vein morphology', 0.4166666666666667, 7.803720102857406, 1.8032054910234865, 'HP:0033353', 'Abnormal blood vessel morphology'),
(465844, 'HP:0032090', 'Intralamellar aortic medial fibrosis', 'XPO:0102329', 'abnormal caudal artery morphology', 0.5081967213114754, 9.604719529875187, 2.2093182147890933, 'UPHENO:0076809', 'abnormal aorta morphology'),
(465845, 'HP:0032090', 'Intralamellar aortic medial fibrosis', 'XPO:0129627', 'increased size of the ventral aorta', 0.4305555555555556, 9.604719529875187, 2.0335597736827666, 'UPHENO:0076809', 'abnormal aorta morphology'),
(465846, 'HP:0032090', 'Intralamellar aortic medial fibrosis', 'XPO:0101840', 'abnormal ventral aorta morphology', 0.5, 9.604719529875187, 2.19142870405076, 'UPHENO:0076809', 'abnormal aorta morphology'),
(465847, 'HP:0032090', 'Intralamellar aortic medial fibrosis', 'XPO:0139829', 'abnormally necrotic artery', 0.41379310344827586, 6.974839882869777, 1.6988645152534954, 'UPHENO:0087186', 'abnormal blood vessel morphology'),
(465848, 'HP:0032090', 'Intralamellar aortic medial fibrosis', 'XPO:0141554', 'abnormal blood vessel morphology in the regenerating hindlimb', 0.4444444444444444, 6.974839882869777, 1.7606614770679263, 'UPHENO:0087186', 'abnormal blood vessel morphology'),
(465849, 'HP:0032090', 'Intralamellar aortic medial fibrosis', 'XPO:0103212', 'abnormal cutaneous magnus morphology', 0.4166666666666667, 7.803720102857406, 1.8032054910234865, 'HP:0033353', 'Abnormal blood vessel morphology'),
(465850, 'HP:0032090', 'Intralamellar aortic medial fibrosis', 'XPO:0101774', 'abnormal paired dorsal aorta morphology', 0.543859649122807, 9.604719529875187, 2.2855238772414723, 'UPHENO:0076809', 'abnormal aorta morphology'),
(465851, 'HP:0032090', 'Intralamellar aortic medial fibrosis', 'XPO:0140133', 'abnormally necrotic dorsal aorta', 0.44285714285714284, 9.604719529875187, 2.0624060339672994, 'UPHENO:0076809', 'abnormal aorta morphology'),
(465852, 'HP:0032090', 'Intralamellar aortic medial fibrosis', 'XPO:0102554', 'abnormal lymph vessel morphology', 0.40350877192982454, 6.65602285090012, 1.6388299504535415, 'HP:0025015', 'Abnormal vascular morphology'),
(465853, 'HP:0032090', 'Intralamellar aortic medial fibrosis', 'XPO:0139802', 'abnormally necrotic ventral aorta', 0.44285714285714284, 9.604719529875187, 2.0624060339672994, 'UPHENO:0076809', 'abnormal aorta morphology'),
(465854, 'HP:0032090', 'Intralamellar aortic medial fibrosis', 'XPO:0102875', 'abnormal vertebral artery morphology', 0.4444444444444444, 6.974839882869777, 1.7606614770679263, 'UPHENO:0087186', 'abnormal blood vessel morphology'),
(465855, 'HP:0032090', 'Intralamellar aortic medial fibrosis', 'XPO:0102613', 'abnormal dorsal longitudinal anastomosing vessel morphology', 0.48, 6.974839882869777, 1.8297330799265483, 'UPHENO:0087186', 'abnormal blood vessel morphology'),
(465856, 'HP:0032090', 'Intralamellar aortic medial fibrosis', 'XPO:0102889', 'abnormal coeliaco-mesenteric artery morphology', 0.4067796610169492, 6.974839882869777, 1.6844058309093048, 'UPHENO:0087186', 'abnormal blood vessel morphology'),
(465857, 'HP:0032090', 'Intralamellar aortic medial fibrosis', 'XPO:0140809', 'abnormally necrotic truncus arteriosus', 0.42857142857142855, 6.974839882869777, 1.7289352482549702, 'UPHENO:0087186', 'abnormal blood vessel morphology'),
(465858, 'HP:0032090', 'Intralamellar aortic medial fibrosis', 'XPO:0139730', 'abnormally necrotic vein', 0.423728813559322, 7.803720102857406, 1.818422684782831, 'HP:0033353', 'Abnormal blood vessel morphology'),
(465859, 'HP:0032090', 'Intralamellar aortic medial fibrosis', 'XPO:0101712', 'abnormal aorta morphology', 0.5636363636363636, 9.604719529875187, 2.326707800641502, 'UPHENO:0076809', 'abnormal aorta morphology'),
(465860, 'HP:0032090', 'Intralamellar aortic medial fibrosis', 'XPO:0130819', 'increased size of the caudal artery', 0.44285714285714284, 9.604719529875187, 2.0624060339672994, 'UPHENO:0076809', 'abnormal aorta morphology'),
(465861, 'HP:0010892', 'Abnormal circulating branched chain amino acid concentration', 'XPO:0141888', 'abnormal threonine metabolic process', 0.625, 10.007478699375595, 2.5009346627030755, 'UPHENO:0051195', 'abnormal amino acid metabolic process'),
(465862, 'HP:0010892', 'Abnormal circulating branched chain amino acid concentration', 'XPO:0141873', 'abnormal tricarboxylic acid metabolic process', 0.5645161290322581, 9.119292702704945, 2.2689177631732522, 'HP:0004354', 'Abnormal circulating carboxylic acid concentration'),
(465863, 'HP:0010892', 'Abnormal circulating branched chain amino acid concentration', 'XPO:0141847', 'abnormal arginine metabolic process', 0.625, 10.007478699375595, 2.5009346627030755, 'UPHENO:0051195', 'abnormal amino acid metabolic process'),
(465864, 'HP:0010892', 'Abnormal circulating branched chain amino acid concentration', 'XPO:0141895', 'abnormal leucine metabolic process', 0.6507936507936508, 12.890121748737435, 2.896344142541676, 'UPHENO:0078596', 'abnormal branched-chain amino acid metabolic process'),
(465865, 'HP:0010892', 'Abnormal circulating branched chain amino acid concentration', 'XPO:0141868', 'abnormal asparagine metabolic process', 0.625, 10.007478699375595, 2.5009346627030755, 'UPHENO:0051195', 'abnormal amino acid metabolic process'),
(465866, 'HP:0010892', 'Abnormal circulating branched chain amino acid concentration', 'XPO:0141869', 'abnormal alpha-amino acid metabolic process', 0.6557377049180327, 10.007478699375595, 2.561694969028251, 'UPHENO:0051195', 'abnormal amino acid metabolic process'),
(465867, 'HP:0010892', 'Abnormal circulating branched chain amino acid concentration', 'XPO:0141848', 'abnormal proline metabolic process', 0.625, 10.007478699375595, 2.5009346627030755, 'UPHENO:0051195', 'abnormal amino acid metabolic process'),
(465868, 'HP:0010892', 'Abnormal circulating branched chain amino acid concentration', 'XPO:0141843', 'abnormal alanine metabolic process', 0.6349206349206349, 10.007478699375595, 2.520705204850873, 'UPHENO:0051195', 'abnormal amino acid metabolic process'),
(465869, 'HP:0010892', 'Abnormal circulating branched chain amino acid concentration', 'XPO:0141912', 'abnormal D-serine metabolic process', 0.6153846153846154, 10.007478699375595, 2.4816221369066205, 'UPHENO:0051195', 'abnormal amino acid metabolic process'),
(465870, 'HP:0010892', 'Abnormal circulating branched chain amino acid concentration', 'XPO:0141896', 'abnormal lysine metabolic process', 0.625, 10.007478699375595, 2.5009346627030755, 'UPHENO:0051195', 'abnormal amino acid metabolic process'),
(465871, 'HP:0010892', 'Abnormal circulating branched chain amino acid concentration', 'XPO:0141917', 'abnormal tryptophan metabolic process', 0.625, 10.007478699375595, 2.5009346627030755, 'UPHENO:0051195', 'abnormal amino acid metabolic process'),
(465872, 'HP:0010892', 'Abnormal circulating branched chain amino acid concentration', 'XPO:0141922', 'abnormal valine metabolic process', 0.6507936507936508, 12.890121748737435, 2.896344142541676, 'UPHENO:0078596', 'abnormal branched-chain amino acid metabolic process'),
(465873, 'HP:0010892', 'Abnormal circulating branched chain amino acid concentration', 'XPO:0141905', 'abnormal ornithine metabolic process', 0.6349206349206349, 10.007478699375595, 2.520705204850873, 'UPHENO:0051195', 'abnormal amino acid metabolic process'),
(465874, 'HP:0010892', 'Abnormal circulating branched chain amino acid concentration', 'XPO:0141882', 'abnormal gamma-aminobutyric acid metabolic process', 0.6451612903225806, 10.007478699375595, 2.5409521582597536, 'UPHENO:0051195', 'abnormal amino acid metabolic process'),
(465875, 'HP:0010892', 'Abnormal circulating branched chain amino acid concentration', 'XPO:0141853', 'abnormal glutamate metabolic process', 0.6060606060606061, 10.007478699375595, 2.4627502117921294, 'UPHENO:0051195', 'abnormal amino acid metabolic process'),
(465876, 'HP:0010892', 'Abnormal circulating branched chain amino acid concentration', 'XPO:0141913', 'abnormal L-serine metabolic process', 0.6153846153846154, 10.007478699375595, 2.4816221369066205, 'UPHENO:0051195', 'abnormal amino acid metabolic process'),
(465877, 'HP:0010892', 'Abnormal circulating branched chain amino acid concentration', 'XPO:0141893', 'abnormal isoleucine metabolic process', 0.6507936507936508, 12.890121748737435, 2.896344142541676, 'UPHENO:0078596', 'abnormal branched-chain amino acid metabolic process'),
(465878, 'HP:0010892', 'Abnormal circulating branched chain amino acid concentration', 'XPO:0141889', 'abnormal homoserine metabolic process', 0.6153846153846154, 10.007478699375595, 2.4816221369066205, 'UPHENO:0051195', 'abnormal amino acid metabolic process'),
(465879, 'HP:0010892', 'Abnormal circulating branched chain amino acid concentration', 'XPO:0141858', 'abnormal serine family amino acid metabolic process', 0.6349206349206349, 10.007478699375595, 2.520705204850873, 'UPHENO:0051195', 'abnormal amino acid metabolic process'),
(465880, 'HP:0010892', 'Abnormal circulating branched chain amino acid concentration', 'XPO:0141887', 'abnormal histidine metabolic process', 0.625, 10.007478699375595, 2.5009346627030755, 'UPHENO:0051195', 'abnormal amino acid metabolic process'),
(465881, 'HP:0010892', 'Abnormal circulating branched chain amino acid concentration', 'XPO:0141918', 'abnormal tyrosine metabolic process', 0.625, 10.007478699375595, 2.5009346627030755, 'UPHENO:0051195', 'abnormal amino acid metabolic process'),
(465882, 'HP:0010892', 'Abnormal circulating branched chain amino acid concentration', 'XPO:0141857', 'abnormal glycine metabolic process', 0.6153846153846154, 10.007478699375595, 2.4816221369066205, 'UPHENO:0051195', 'abnormal amino acid metabolic process'),
(465883, 'HP:0003148', 'Elevated serum acid phosphatase', 'XPO:0131687', 'abnormal astral microtubule', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(465884, 'HP:0003148', 'Elevated serum acid phosphatase', 'XPO:0100004', 'abnormal cell', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(465885, 'HP:0003148', 'Elevated serum acid phosphatase', 'XPO:0100899', 'abnormal secondary spermatogonium', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(465886, 'HP:0003148', 'Elevated serum acid phosphatase', 'XPO:0100477', 'abnormal pericyte', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(465887, 'HP:0003148', 'Elevated serum acid phosphatase', 'XPO:0101575', 'abnormal vitelline membrane', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(465888, 'HP:0003148', 'Elevated serum acid phosphatase', 'XPO:0101409', 'abnormal perivitelline space', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(465889, 'HP:0003148', 'Elevated serum acid phosphatase', 'XPO:0100337', 'abnormal zygote', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(465890, 'HP:0003148', 'Elevated serum acid phosphatase', 'XPO:0100503', 'abnormal blastomere D2', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(465891, 'HP:0003148', 'Elevated serum acid phosphatase', 'XPO:0100638', 'abnormal polar body', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(465892, 'HP:0003148', 'Elevated serum acid phosphatase', 'XPO:0100547', 'abnormal blastomere V2', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(465893, 'HP:0003148', 'Elevated serum acid phosphatase', 'XPO:0100784', 'abnormal left blastomere', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(465894, 'HP:0003148', 'Elevated serum acid phosphatase', 'XPO:0100285', 'abnormal progenitor cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(465895, 'HP:0003148', 'Elevated serum acid phosphatase', 'XPO:0131669', 'abnormal Roux spot', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(465896, 'HP:0003148', 'Elevated serum acid phosphatase', 'XPO:0131685', 'abnormal cortical actin cytoskeleton', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(465897, 'HP:0003148', 'Elevated serum acid phosphatase', 'XPO:0101333', 'abnormal barrier epithelial cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(465898, 'HP:0003148', 'Elevated serum acid phosphatase', 'XPO:0101061', 'abnormal plasma membrane', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(465899, 'HP:0003148', 'Elevated serum acid phosphatase', 'XPO:0101463', 'abnormal right-ventral blastomere', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(465900, 'HP:0003148', 'Elevated serum acid phosphatase', 'XPO:0100551', 'abnormal oocyte cortex', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(465901, 'HP:0003148', 'Elevated serum acid phosphatase', 'XPO:0100307', 'abnormal blastomere', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(465902, 'HP:0003148', 'Elevated serum acid phosphatase', 'XPO:0100533', 'abnormal melanoblast', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(465903, 'HP:0003148', 'Elevated serum acid phosphatase', 'XPO:0100437', 'abnormal proepicardium', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(465904, 'HP:0003148', 'Elevated serum acid phosphatase', 'XPO:0101468', 'abnormal stage I oocyte', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(465905, 'HP:0003148', 'Elevated serum acid phosphatase', 'XPO:0100902', 'abnormal spermatocyte', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(465906, 'HP:0003148', 'Elevated serum acid phosphatase', 'XPO:0131735', 'abnormal spindle assembly', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(465907, 'HP:0003148', 'Elevated serum acid phosphatase', 'XPO:0100392', 'abnormal cilium', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(465908, 'HP:0003148', 'Elevated serum acid phosphatase', 'XPO:0101480', 'abnormal stage V oocyte', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(465909, 'HP:0003148', 'Elevated serum acid phosphatase', 'XPO:0101283', 'abnormal left-ventral blastomere', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(465910, 'HP:0003148', 'Elevated serum acid phosphatase', 'XPO:0101240', 'abnormal ciliated non-epidermal cell', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(465911, 'HP:0003148', 'Elevated serum acid phosphatase', 'XPO:0100956', 'abnormal centrosome', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(465912, 'HP:0003148', 'Elevated serum acid phosphatase', 'XPO:0101472', 'abnormal zygote cortex', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(465913, 'HP:0003148', 'Elevated serum acid phosphatase', 'XPO:0131675', 'abnormal spindle microtubule', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(465914, 'HP:0003148', 'Elevated serum acid phosphatase', 'XPO:0100626', 'abnormal primordial germ cell', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(465915, 'HP:0003148', 'Elevated serum acid phosphatase', 'XPO:0100721', 'abnormal centromere', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(465916, 'HP:0003148', 'Elevated serum acid phosphatase', 'XPO:0100172', 'abnormal stem cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(465917, 'HP:0003148', 'Elevated serum acid phosphatase', 'XPO:0100108', 'abnormal cell part', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(465918, 'HP:0003148', 'Elevated serum acid phosphatase', 'XPO:0131677', 'abnormal actin filament', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(465919, 'HP:0003148', 'Elevated serum acid phosphatase', 'XPO:0131666', 'abnormal adherens junction', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(465920, 'HP:0003148', 'Elevated serum acid phosphatase', 'XPO:0100704', 'abnormal Merkel cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(465921, 'HP:0003148', 'Elevated serum acid phosphatase', 'XPO:0101461', 'abnormal sperm entry point', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(465922, 'HP:0003148', 'Elevated serum acid phosphatase', 'XPO:0100862', 'abnormal blastomere V1', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(465923, 'HP:0003148', 'Elevated serum acid phosphatase', 'XPO:0101378', 'abnormal blastomere D1', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(465924, 'HP:0003148', 'Elevated serum acid phosphatase', 'XPO:0100026', 'abnormal germ cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(465925, 'HP:0003148', 'Elevated serum acid phosphatase', 'XPO:0100025', 'abnormal oocyte', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(465926, 'HP:0003148', 'Elevated serum acid phosphatase', 'XPO:0100691', 'abnormal keratin accumulating cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(465927, 'HP:0003148', 'Elevated serum acid phosphatase', 'XPO:0101302', 'abnormal subcortical cytoplasm', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(465928, 'HP:0003148', 'Elevated serum acid phosphatase', 'XPO:0100791', 'abnormal multiciliated cell precursor', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(465929, 'HP:0003148', 'Elevated serum acid phosphatase', 'XPO:0101264', 'abnormal mitotic spindle', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(465930, 'HP:0003148', 'Elevated serum acid phosphatase', 'XPO:0100653', 'abnormal myoblast', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(465931, 'HP:0003148', 'Elevated serum acid phosphatase', 'XPO:0101373', 'abnormal oxygen accumulating cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(465932, 'HP:0003148', 'Elevated serum acid phosphatase', 'XPO:0131708', 'abnormal cilium disassembly', 0.42857142857142855, 5.835653092541957, 1.5814531869511603, 'HP:0011017', 'Abnormal cellular physiology'),
(465933, 'HP:0003148', 'Elevated serum acid phosphatase', 'XPO:0100802', 'abnormal exocrine cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(465934, 'HP:0003148', 'Elevated serum acid phosphatase', 'XPO:0101004', 'abnormal acid secreting cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(465935, 'HP:0003148', 'Elevated serum acid phosphatase', 'XPO:0101136', 'abnormal ooplasm', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(465936, 'HP:0003148', 'Elevated serum acid phosphatase', 'XPO:0101297', 'abnormal barrier cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(465937, 'HP:0003148', 'Elevated serum acid phosphatase', 'XPO:0131667', 'abnormal actin cytoskeleton', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(465938, 'HP:0003148', 'Elevated serum acid phosphatase', 'XPO:0100842', 'abnormal left-dorsal blastomere', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(465939, 'HP:0003148', 'Elevated serum acid phosphatase', 'XPO:0101072', 'abnormal mitochondrial cloud', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(465940, 'HP:0003148', 'Elevated serum acid phosphatase', 'XPO:0107284', 'abnormal migrating myoblast', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(465941, 'HP:0003148', 'Elevated serum acid phosphatase', 'XPO:0101071', 'abnormal endoplasmic reticulum', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(465942, 'HP:0003148', 'Elevated serum acid phosphatase', 'XPO:0100515', 'abnormal somatic stem cell', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(465943, 'HP:0003148', 'Elevated serum acid phosphatase', 'XPO:0101405', 'abnormal ring structure', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(465944, 'HP:0003148', 'Elevated serum acid phosphatase', 'XPO:0107312', 'abnormal filopodium', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(465945, 'HP:0003148', 'Elevated serum acid phosphatase', 'XPO:0100429', 'abnormal spermatid', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(465946, 'HP:0003148', 'Elevated serum acid phosphatase', 'XPO:0142057', 'abnormal desmosome', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(465947, 'HP:0003148', 'Elevated serum acid phosphatase', 'XPO:0101326', 'abnormal cementoblast', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(465948, 'HP:0003148', 'Elevated serum acid phosphatase', 'XPO:0101228', 'abnormal mesenchymal stem cell', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(465949, 'HP:0003148', 'Elevated serum acid phosphatase', 'XPO:0101237', 'abnormal mucus secreting cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(465950, 'HP:0003148', 'Elevated serum acid phosphatase', 'XPO:0101497', 'abnormal ciliary axoneme', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(465951, 'HP:0003148', 'Elevated serum acid phosphatase', 'XPO:0100574', 'abnormal gastrula cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(465952, 'HP:0003148', 'Elevated serum acid phosphatase', 'XPO:0101220', 'abnormal centriole', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(465953, 'HP:0003148', 'Elevated serum acid phosphatase', 'XPO:0100989', 'abnormal right blastomere', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(465954, 'HP:0003148', 'Elevated serum acid phosphatase', 'XPO:0100715', 'abnormal ciliated cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(465955, 'HP:0003148', 'Elevated serum acid phosphatase', 'XPO:0101435', 'abnormal paracrine cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(465956, 'HP:0003148', 'Elevated serum acid phosphatase', 'XPO:0101448', 'abnormal myelin accumulating cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(465957, 'HP:0003148', 'Elevated serum acid phosphatase', 'XPO:0100549', 'abnormal mitotic cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(465958, 'HP:0003148', 'Elevated serum acid phosphatase', 'XPO:0101513', 'abnormal basal body', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(465959, 'HP:0003148', 'Elevated serum acid phosphatase', 'XPO:0101311', 'abnormal bottle cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(465960, 'HP:0003148', 'Elevated serum acid phosphatase', 'XPO:0100907', 'abnormal cytoplasm', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(465961, 'HP:0003148', 'Elevated serum acid phosphatase', 'XPO:0100894', 'abnormal nucleus', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(465962, 'HP:0003148', 'Elevated serum acid phosphatase', 'XPO:0101467', 'abnormal alkali secreting cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(465963, 'HP:0003148', 'Elevated serum acid phosphatase', 'XPO:0131706', 'abnormal ciliary basal body organization', 0.42857142857142855, 5.835653092541957, 1.5814531869511603, 'HP:0011017', 'Abnormal cellular physiology'),
(465964, 'HP:0003148', 'Elevated serum acid phosphatase', 'XPO:0101389', 'abnormal wedge region', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(465965, 'HP:0003148', 'Elevated serum acid phosphatase', 'XPO:0100888', 'abnormal microtubule', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(465966, 'HP:0003148', 'Elevated serum acid phosphatase', 'XPO:0101498', 'abnormal stage II oocyte', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(465967, 'HP:0003148', 'Elevated serum acid phosphatase', 'XPO:0101241', 'abnormal nucleate erythrocyte', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(465968, 'HP:0003148', 'Elevated serum acid phosphatase', 'XPO:0131707', 'abnormal cilium assembly', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(465969, 'HP:0003148', 'Elevated serum acid phosphatase', 'XPO:0101113', 'abnormal stage IV oocyte', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(465970, 'HP:0003148', 'Elevated serum acid phosphatase', 'XPO:0100308', 'abnormal early embryonic cell', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(465971, 'HP:0003148', 'Elevated serum acid phosphatase', 'XPO:0101547', 'abnormal lampbrush chromosome', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(465972, 'HP:0003148', 'Elevated serum acid phosphatase', 'XPO:0101366', 'abnormal morula cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(465973, 'HP:0003148', 'Elevated serum acid phosphatase', 'XPO:0101535', 'abnormal absorptive cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(465974, 'HP:0003148', 'Elevated serum acid phosphatase', 'XPO:0126318', 'abnormally localised cell', 0.4117647058823529, 3.6715585125471644, 1.229560169755361, 'UPHENO:0086172', 'abnormal cell'),
(465975, 'HP:0003148', 'Elevated serum acid phosphatase', 'XPO:0100289', 'abnormal chondroblast', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(465976, 'HP:0003148', 'Elevated serum acid phosphatase', 'XPO:0103642', 'increased cell population proliferation', 0.40540540540540543, 5.835653092541957, 1.5381174557839463, 'HP:0011017', 'Abnormal cellular physiology'),
(465977, 'HP:0003148', 'Elevated serum acid phosphatase', 'XPO:0100176', 'abnormal stage VI oocyte', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(465978, 'HP:0003148', 'Elevated serum acid phosphatase', 'XPO:0101132', 'abnormal apoptotic cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(465979, 'HP:0003148', 'Elevated serum acid phosphatase', 'XPO:0115758', 'abnormally decreased mobility of melanoblast', 0.4375, 3.6715585125471644, 1.2674016132384338, 'UPHENO:0086172', 'abnormal cell'),
(465980, 'HP:0003148', 'Elevated serum acid phosphatase', 'XPO:0100754', 'abnormal electrically active cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(465981, 'HP:0003148', 'Elevated serum acid phosphatase', 'XPO:0100887', 'abnormal right-dorsal blastomere', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(465982, 'HP:0003148', 'Elevated serum acid phosphatase', 'XPO:0101740', 'abnormal cell part morphology', 0.4117647058823529, 3.6715585125471644, 1.229560169755361, 'UPHENO:0086172', 'abnormal cell'),
(465983, 'HP:0003148', 'Elevated serum acid phosphatase', 'XPO:0100674', 'abnormal secondary oogonium', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(465984, 'HP:0003148', 'Elevated serum acid phosphatase', 'XPO:0100724', 'abnormal kinetochore', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(465985, 'HP:0003148', 'Elevated serum acid phosphatase', 'XPO:0100218', 'abnormal epithelial cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(465986, 'HP:0003148', 'Elevated serum acid phosphatase', 'XPO:0107339', 'abnormal yolk platelet', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(465987, 'HP:0003148', 'Elevated serum acid phosphatase', 'XPO:0100917', 'abnormal stage III oocyte', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(465988, 'HP:0003148', 'Elevated serum acid phosphatase', 'XPO:0100976', 'abnormal multiciliated cell', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(465989, 'HP:0100938', 'Sclerosis of the middle phalanx of the 5th toe', 'XPO:0102566', 'abnormal claw primordium morphology', 0.42105263157894735, 7.639349617137506, 1.793479372573705, 'UPHENO:0088132', 'abnormal pedal digit morphology'),
(465990, 'HP:0100938', 'Sclerosis of the middle phalanx of the 5th toe', 'XPO:0102880', 'abnormal digit-joint region morphology', 0.4074074074074074, 6.466375519622663, 1.6230986679103019, 'UPHENO:0086700', 'abnormal digit morphology'),
(465991, 'HP:0100938', 'Sclerosis of the middle phalanx of the 5th toe', 'XPO:0102180', 'abnormal hindlimb digit 3 morphology', 0.40816326530612246, 7.639349617137506, 1.7658147933874382, 'HP:0001780', 'Abnormal toe morphology'),
(465992, 'HP:0100938', 'Sclerosis of the middle phalanx of the 5th toe', 'XPO:0102051', 'abnormal hindlimb digit 2 morphology', 0.40816326530612246, 7.639349617137506, 1.7658147933874382, 'UPHENO:0088132', 'abnormal pedal digit morphology'),
(465993, 'HP:0100938', 'Sclerosis of the middle phalanx of the 5th toe', 'XPO:0101872', 'abnormal hindlimb digit 1 morphology', 0.40816326530612246, 7.639349617137506, 1.7658147933874382, 'HP:0001780', 'Abnormal toe morphology'),
(465994, 'HP:0100938', 'Sclerosis of the middle phalanx of the 5th toe', 'XPO:0102876', 'abnormal hindlimb digit 4 morphology', 0.40816326530612246, 7.639349617137506, 1.7658147933874382, 'UPHENO:0088132', 'abnormal pedal digit morphology'),
(465995, 'HP:0100938', 'Sclerosis of the middle phalanx of the 5th toe', 'XPO:0101809', 'abnormal hindlimb digit morphology', 0.4166666666666667, 7.639349617137506, 1.7841138810272064, 'HP:0001780', 'Abnormal toe morphology'),
(465996, 'HP:0100938', 'Sclerosis of the middle phalanx of the 5th toe', 'XPO:0102948', 'abnormal hindlimb digit 5 morphology', 0.40816326530612246, 7.639349617137506, 1.7658147933874382, 'UPHENO:0088132', 'abnormal pedal digit morphology'),
(465997, 'HP:0100938', 'Sclerosis of the middle phalanx of the 5th toe', 'XPO:0101810', 'abnormal digit morphology', 0.4074074074074074, 6.466375519622663, 1.6230986679103019, 'UPHENO:0086700', 'abnormal digit morphology'),
(465998, 'HP:0002265', 'Large fleshy ears', 'XPO:0141835', 'edematous head', 0.40384615384615385, 4.5318002188002176, 1.3528303989641963, 'UPHENO:0087907', 'abnormal head morphology'),
(465999, 'HP:0002265', 'Large fleshy ears', 'XPO:0102259', 'abnormal pharyngeal region morphology', 0.42857142857142855, 4.5318002188002176, 1.3936283915633758, 'UPHENO:0087907', 'abnormal head morphology'),
(466000, 'HP:0002265', 'Large fleshy ears', 'XPO:0103358', 'decreased size of the pharyngeal region', 0.41509433962264153, 4.6864066944795475, 1.3947404389520346, 'UPHENO:0075195', 'abnormal size of anatomical entity'),
(466001, 'HP:0002265', 'Large fleshy ears', 'XPO:0130703', 'increased size of the circumpharyngeal ridge', 0.42105263157894735, 5.972749669260594, 1.585825326448175, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(466002, 'HP:0002265', 'Large fleshy ears', 'XPO:0140335', 'abnormally necrotic pharyngeal region', 0.40384615384615385, 4.5318002188002176, 1.3528303989641963, 'UPHENO:0087907', 'abnormal head morphology'),
(466003, 'HP:0002265', 'Large fleshy ears', 'XPO:0130787', 'increased size of the lateral nasal prominence', 0.42857142857142855, 5.972749669260594, 1.5999218287949384, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(466004, 'HP:0002265', 'Large fleshy ears', 'XPO:0131638', 'increased size of the intercanthal region', 0.4444444444444444, 5.972749669260594, 1.629280641436663, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(466005, 'HP:0002265', 'Large fleshy ears', 'XPO:0142045', 'increased size of the nasal region', 0.42105263157894735, 5.972749669260594, 1.585825326448175, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(466006, 'HP:0002265', 'Large fleshy ears', 'XPO:0101634', 'abnormal head morphology', 0.42, 4.5318002188002176, 1.3796217205799897, 'UPHENO:0087907', 'abnormal head morphology'),
(466007, 'HP:0002265', 'Large fleshy ears', 'XPO:0130062', 'increased size of the head region', 0.4444444444444444, 5.972749669260594, 1.629280641436663, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(466008, 'HP:0002265', 'Large fleshy ears', 'XPO:0129591', 'increased size of the auditory apparatus', 0.4117647058823529, 7.26295268789559, 1.7293431057395094, 'UPHENO:0076730', 'abnormal ear morphology'),
(466009, 'HP:0002265', 'Large fleshy ears', 'XPO:0126939', 'abnormally localised auditory apparatus', 0.5, 10.484129389061598, 2.289555567032781, 'UPHENO:0005986', 'abnormal shape of external ear'),
(466010, 'HP:0002265', 'Large fleshy ears', 'XPO:0130309', 'increased size of the auditory tube', 0.4057971014492754, 7.26295268789559, 1.7167658980511158, 'UPHENO:0076730', 'abnormal ear morphology'),
(466011, 'HP:0002265', 'Large fleshy ears', 'XPO:0130295', 'increased size of the hatching gland primordium', 0.4067796610169492, 5.972749669260594, 1.5587152035573786, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(466012, 'HP:0002265', 'Large fleshy ears', 'XPO:0130273', 'increased size of the pharyngeal pouch', 0.42105263157894735, 5.972749669260594, 1.585825326448175, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(466013, 'HP:0002265', 'Large fleshy ears', 'XPO:0102224', 'abnormal auditory apparatus morphology', 0.4032258064516129, 7.26295268789559, 1.711318192153817, 'UPHENO:0076730', 'abnormal ear morphology'),
(466014, 'HP:0002265', 'Large fleshy ears', 'XPO:0142059', 'abnormal nasal region morphology', 0.4117647058823529, 4.5318002188002176, 1.3660290568695288, 'UPHENO:0087907', 'abnormal head morphology'),
(466015, 'HP:0002265', 'Large fleshy ears', 'XPO:0103739', 'increased size of the pharyngeal region', 0.47058823529411764, 5.972749669260594, 1.6765159488388017, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(466016, 'HP:0002265', 'Large fleshy ears', 'XPO:0130640', 'increased size of the medial nasal prominence', 0.42857142857142855, 5.972749669260594, 1.5999218287949384, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(466017, 'HP:0002265', 'Large fleshy ears', 'XPO:0115526', 'abnormally incomplete structure of head', 0.4117647058823529, 4.5318002188002176, 1.3660290568695288, 'UPHENO:0087907', 'abnormal head morphology'),
(466018, 'HP:0002265', 'Large fleshy ears', 'XPO:0141839', 'edematous pharyngeal region', 0.4117647058823529, 4.5318002188002176, 1.3660290568695288, 'UPHENO:0087907', 'abnormal head morphology'),
(466019, 'HP:0002265', 'Large fleshy ears', 'XPO:0141298', 'abnormal intercanthal region morphology', 0.40384615384615385, 4.5318002188002176, 1.3528303989641963, 'UPHENO:0087907', 'abnormal head morphology'),
(466020, 'HP:0002265', 'Large fleshy ears', 'XPO:0130319', 'increased size of the craniofacial region', 0.42105263157894735, 5.972749669260594, 1.585825326448175, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(466021, 'HP:0002265', 'Large fleshy ears', 'XPO:0129785', 'increased size of the tympanic disk', 0.40425531914893614, 14.890121748737435, 2.4534487807375087, 'UPHENO:0001251', 'increased size of the external ear'),
(466022, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100032', 'abnormal nervous system', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(466023, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0101362', 'abnormal vegetal cortex', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(466024, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100551', 'abnormal oocyte cortex', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(466025, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100860', 'abnormal parathyroid', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(466026, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0141892', 'abnormal inositol metabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(466027, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100156', 'abnormal foregut', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(466028, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0101366', 'abnormal morula cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(466029, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100900', 'abnormal angioblast', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(466030, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0101480', 'abnormal stage V oocyte', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(466031, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100916', 'abnormal principal cavity', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(466032, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100858', 'abnormal presumptive midbrain-hindbrain boundary', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(466033, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0107269', 'abnormal right side', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466034, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0107268', 'abnormal left side', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466035, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0107262', 'abnormal left-right axis', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466036, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0141798', 'abnormal lipid metabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(466037, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0133403', 'abnormal developmental process', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(466038, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0101078', 'abnormal mucous gland', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466039, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0124719', 'absent anatomical structure', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466040, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100822', 'abnormal hindlimb zeugopod', 0.48148148148148145, 5.504475013697824, 1.6279750564345348, 'HP:0040064', 'Abnormality of limbs'),
(466041, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0131666', 'abnormal adherens junction', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(466042, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0101241', 'abnormal nucleate erythrocyte', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(466043, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0101500', 'abnormal endodermal cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(466044, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100722', 'abnormal barbel', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466045, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0101264', 'abnormal mitotic spindle', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(466046, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100816', 'abnormal blastocoel anlage', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466047, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0133388', 'absent insulin receptor signaling pathway', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(466048, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0107261', 'abnormal dorsal-ventral axis', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466049, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0101099', 'abnormal ventro-lateral marginal zone', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466050, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0126318', 'abnormally localised cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(466051, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100670', 'abnormal forelimb zeugopod', 0.48148148148148145, 5.504475013697824, 1.6279750564345348, 'HP:0040064', 'Abnormality of limbs'),
(466052, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0102484', 'abnormal interdigital region morphology', 0.4482758620689655, 5.504475013697824, 1.570835217966058, 'HP:0040064', 'Abnormality of limbs'),
(466053, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0141748', 'abnormal gas homeostasis', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(466054, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0141770', 'abnormal urate homeostasis', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(466055, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0101837', 'abnormal limb segment morphology', 0.40625, 5.504475013697824, 1.4953905758412218, 'HP:0040064', 'Abnormality of limbs'),
(466056, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100031', 'abnormal central nervous system', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(466057, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0101113', 'abnormal stage IV oocyte', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(466058, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100416', 'abnormal ligament', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(466059, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100014', 'abnormal tissue', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466060, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100423', 'abnormal process', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466061, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100616', 'abnormal ventral blood island', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(466062, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100239', 'abnormal acellular anatomical structure', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466063, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0101448', 'abnormal myelin accumulating cell', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(466064, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100176', 'abnormal stage VI oocyte', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(466065, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100985', 'abnormal simple columnar epithelium', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466066, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100843', 'abnormal fasciculated network of fibrils', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(466067, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100251', 'abnormal proteinaceous extracellular matrix', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466068, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0141783', 'abnormal collagen metabolic process', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(466069, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0101092', 'abnormal dorso-lateral marginal zone', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466070, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100599', 'abnormal adult immune system', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(466071, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0107253', 'abnormal enteric nervous system', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(466072, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0141794', 'abnormal prosthetic group metabolic process', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(466073, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100135', 'abnormal surface structure', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466074, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100023', 'abnormal mesenchyme', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466075, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0141264', 'abnormal schooling behavior', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(466076, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100754', 'abnormal electrically active cell', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(466077, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100403', 'abnormal forelimb', 0.5416666666666666, 5.504475013697824, 1.7267283030111178, 'HP:0040064', 'Abnormality of limbs'),
(466078, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0101240', 'abnormal ciliated non-epidermal cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(466079, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0101349', 'abnormal trunk region', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466080, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100864', 'abnormal dorsolateral ascending neuron', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(466081, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100888', 'abnormal microtubule', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(466082, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100002', 'abnormal head', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(466083, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100523', 'abnormal midgut', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(466084, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100146', 'abnormal primary germ layer', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466085, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0107258', 'abnormal anatomical axis', 0.5294117647058824, 1.706362323152461, 0.9504568842024205, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466086, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100585', 'abnormal elastica externa', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(466087, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0101023', 'abnormal ultimobranchial body', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(466088, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100741', 'abnormal blastopore', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466089, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100114', 'abnormal peripheral nervous system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(466090, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0101333', 'abnormal barrier epithelial cell', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(466091, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100341', 'abnormal hand', 0.48148148148148145, 5.504475013697824, 1.6279750564345348, 'HP:0040064', 'Abnormality of limbs'),
(466092, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100823', 'abnormal blood', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(466093, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100289', 'abnormal chondroblast', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(466094, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100363', 'abnormal cardiovascular system', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466095, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0107278', 'abnormal medial region', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466096, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0131675', 'abnormal spindle microtubule', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(466097, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100393', 'abnormal involuting marginal zone', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466098, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100667', 'abnormal vegetal yolk mass', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466099, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100429', 'abnormal spermatid', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(466100, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100852', 'abnormal interdigital region', 0.6842105263157895, 5.504475013697824, 1.9406750748680988, 'HP:0040064', 'Abnormality of limbs'),
(466101, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0107267', 'abnormal ventral side', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466102, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100856', 'abnormal simple organ', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466103, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100799', 'abnormal genital ridge', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(466104, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100887', 'abnormal right-dorsal blastomere', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(466105, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100009', 'abnormal multi-tissue structure', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466106, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0101441', 'abnormal interdigital webbing', 0.48148148148148145, 5.504475013697824, 1.6279750564345348, 'HP:0040064', 'Abnormality of limbs'),
(466107, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100715', 'abnormal ciliated cell', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(466108, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0101575', 'abnormal vitelline membrane', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(466109, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0101347', 'abnormal hindlimb region', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466110, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100862', 'abnormal blastomere V1', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(466111, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100062', 'abnormal anatomical space', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466112, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0101638', 'abnormal anatomical structure morphology', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466113, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100162', 'abnormal presumptive rhombomere', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466114, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100282', 'abnormal pelvic girdle primordium', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466115, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0101237', 'abnormal mucus secreting cell', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(466116, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100503', 'abnormal blastomere D2', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(466117, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100444', 'abnormal cement gland', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466118, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0131677', 'abnormal actin filament', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(466119, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0107326', 'abnormal regenerating pelvic girdle', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466120, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0101403', 'abnormal basal lamina', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466121, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0116091', 'abnormally increased variability of size of cell in endoderm', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(466122, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0126321', 'abnormally localised anatomical structure', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466123, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0101109', 'abnormal egg cell-free extract', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466124, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0101212', 'abnormal glomeral mesenchyme', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(466125, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0141265', 'abnormal escape behavior', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(466126, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100540', 'abnormal left lymph heart', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(466127, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0101467', 'abnormal alkali secreting cell', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(466128, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100133', 'abnormal solid compound organ', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466129, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100218', 'abnormal epithelial cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(466130, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100175', 'abnormal migrating neuroblast', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(466131, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0101071', 'abnormal endoplasmic reticulum', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(466132, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100060', 'abnormal regenerating tissue', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466133, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100954', 'abnormal neural progenitor cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(466134, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100249', 'abnormal avascular GAG-rich matrix', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466135, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100894', 'abnormal nucleus', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(466136, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100724', 'abnormal kinetochore', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(466137, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100344', 'abnormal portion of organism substance', 0.5625, 1.706362323152461, 0.9797085315405084, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466138, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100557', 'abnormal prime meridian', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466139, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100026', 'abnormal germ cell', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(466140, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0115512', 'abnormally semi-erect whole organism', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466141, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100588', 'abnormal unicellular gland', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466142, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0101450', 'abnormal myeloid cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(466143, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100627', 'abnormal pharyngeal region', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(466144, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100701', 'abnormal microglial cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(466145, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100587', 'abnormal vestibuloauditory system', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(466146, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100842', 'abnormal left-dorsal blastomere', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(466147, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0101451', 'abnormal dorsal lymph space', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(466148, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100867', 'abnormal apical mesenchyme', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466149, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0102113', 'abnormal anatomical line morphology', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466150, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0131745', 'abnormal axis elongation', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(466151, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100734', 'abnormal lateral line system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(466152, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0141743', 'abnormal chemical homeostasis within a tissue', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(466153, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0101221', 'abnormal larval immune system', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(466154, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100537', 'abnormal medium cavity', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(466155, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100956', 'abnormal centrosome', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(466156, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0101377', 'abnormal manicotto glandulare', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(466157, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100533', 'abnormal melanoblast', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(466158, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100511', 'abnormal stylopod', 0.5652173913043478, 5.504475013697824, 1.7638664937410224, 'HP:0040064', 'Abnormality of limbs'),
(466159, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0101136', 'abnormal ooplasm', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(466160, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100108', 'abnormal cell part', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(466161, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100202', 'abnormal embryo', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466162, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0101200', 'abnormal joint region', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466163, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0141781', 'abnormal secondary metabolic process', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(466164, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0101107', 'abnormal erythroid cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(466165, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100638', 'abnormal polar body', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(466166, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0141271', 'increased surface breathing', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(466167, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100084', 'abnormal anatomical group', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466168, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100854', 'abnormal spiracle', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466169, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100545', 'abnormal male organism', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466170, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0107260', 'abnormal anterior-posterior axis', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466171, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100547', 'abnormal blastomere V2', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(466172, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100688', 'abnormal adipose tissue', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(466173, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0101569', 'abnormal activin-induced ectoderm', 0.5294117647058824, 1.706362323152461, 0.9504568842024205, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466174, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0101405', 'abnormal ring structure', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(466175, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0101176', 'abnormal non-ciliated epithelial cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(466176, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100309', 'abnormal vegetal hemisphere', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466177, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100384', 'abnormal amputated tissue', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466178, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100902', 'abnormal spermatocyte', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(466179, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100781', 'abnormal presumptive ectoderm', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466180, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0141499', 'abnormal tadpole', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466181, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0101283', 'abnormal left-ventral blastomere', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(466182, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100664', 'abnormal periocular region', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(466183, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0101083', 'abnormal T cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(466184, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100974', 'abnormal cardiac mesoderm', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466185, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0131723', 'abnormal pathway-restricted SMAD protein phosphorylation', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(466186, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0101373', 'abnormal oxygen accumulating cell', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(466187, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100546', 'abnormal whole organism', 0.5294117647058824, 1.706362323152461, 0.9504568842024205, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466188, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100762', 'abnormal intersomitic region', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466189, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100999', 'abnormal serous membrane', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466190, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0141754', 'abnormal homeostatic process', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(466191, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0101570', 'abnormal forelimb region', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466192, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100293', 'abnormal duct', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466193, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0101472', 'abnormal zygote cortex', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(466194, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0101740', 'abnormal cell part morphology', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(466195, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0101498', 'abnormal stage II oocyte', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(466196, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0142057', 'abnormal desmosome', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(466197, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0141790', 'abnormal cellular metabolic process', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(466198, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0131469', 'abnormal heart process', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(466199, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100457', 'abnormal foot', 0.48148148148148145, 5.504475013697824, 1.6279750564345348, 'HP:0040064', 'Abnormality of limbs'),
(466200, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100691', 'abnormal keratin accumulating cell', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(466201, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100796', 'abnormal pseudoblastema', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466202, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100308', 'abnormal early embryonic cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(466203, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100643', 'abnormal thoracic region', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466204, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0141315', 'abnormal anatomical region', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466205, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100028', 'abnormal anatomical cluster', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466206, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100067', 'abnormal animal hemisphere', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466207, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100265', 'abnormal sensory epithelial cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(466208, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0126653', 'abnormally localised limb', 0.40625, 5.504475013697824, 1.4953905758412218, 'HP:0040064', 'Abnormality of limbs'),
(466209, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0101096', 'abnormal tendon', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(466210, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100482', 'abnormal Mullerian duct', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(466211, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0101396', 'abnormal apical epithelial cap', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466212, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100935', 'abnormal skeleton', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(466213, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100728', 'abnormal cell condensation', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466214, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0107276', 'abnormal dorsal region', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466215, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100807', 'abnormal matrix-based tissue', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466216, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0127101', 'abnormally localised portion of organism substance', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466217, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100274', 'abnormal sensory system', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(466218, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0141738', 'abnormal carbon dioxide homeostasis', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(466219, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100372', 'abnormal hematological system', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(466220, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100120', 'abnormal genital system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(466221, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0141714', 'abnormal anterior notochord', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(466222, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0101976', 'abnormal portion of organism substance morphology', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466223, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100515', 'abnormal somatic stem cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(466224, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100277', 'abnormal blastocoel', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466225, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0101224', 'abnormal dorsal involuting marginal zone', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466226, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0101501', 'abnormal parabrachial area', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(466227, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100553', 'abnormal laryngeal muscle primordium', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466228, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0125007', 'absent anatomical line', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466229, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100465', 'abnormal skeletal system', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(466230, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100468', 'abnormal muscular system', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466231, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0141907', 'abnormal putrescine metabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(466232, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0101411', 'abnormal marginal zone (sensu neural)', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466233, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100377', 'abnormal connective tissue', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(466234, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0101162', 'abnormal stromal cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(466235, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0126624', 'abnormally localised anatomical line', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466236, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100081', 'abnormal anatomical entity in vitro', 0.5625, 1.706362323152461, 0.9797085315405084, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466237, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0142054', 'abnormal digestive tract', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(466238, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0101157', 'abnormal female organism', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466239, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100750', 'abnormal regenerating fin', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466240, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0101269', 'abnormal mesodermal cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(466241, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100610', 'abnormal appendage', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466242, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0107264', 'abnormal anterior side', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466243, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0101435', 'abnormal paracrine cell', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(466244, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0101587', 'abnormal hemangioblast', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(466245, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100735', 'abnormal hindgut', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(466246, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100827', 'abnormal atypical epithelium', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466247, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100205', 'abnormal limb segment', 0.5909090909090909, 5.504475013697824, 1.8035088927632121, 'HP:0040064', 'Abnormality of limbs'),
(466248, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100225', 'abnormal endocrine system', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(466249, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100394', 'abnormal marginal zone', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466250, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0101228', 'abnormal mesenchymal stem cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(466251, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0141267', 'abnormal resting posture', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(466252, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100674', 'abnormal secondary oogonium', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(466253, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100913', 'abnormal Brachets cleft', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466254, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0116494', 'absent biological process', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(466255, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100415', 'abnormal secretory epithelial cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(466256, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100991', 'abnormal iliac process primordium', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466257, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100760', 'abnormal Stirnorgan', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(466258, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100791', 'abnormal multiciliated cell precursor', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(466259, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0131730', 'abnormal regulation of protein folding', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(466260, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100228', 'abnormal skeletal subdivision', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(466261, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0141776', 'abnormal metabolic process', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(466262, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100800', 'abnormal ventral marginal zone', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466263, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100386', 'abnormal limb', 0.6190476190476191, 5.504475013697824, 1.8459502028323378, 'HP:0040064', 'Abnormality of limbs'),
(466264, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0101519', 'abnormal hypobranchial placode', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466265, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0141841', 'abnormality of whole organism mass', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(466266, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100912', 'abnormal trabecula', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466267, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0141772', 'abnormal water homeostasis', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(466268, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100151', 'abnormal primordium', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466269, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100196', 'abnormal neuron', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(466270, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0107259', 'abnormal animal-vegetal axis', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466271, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0101573', 'abnormal peripheral vegetal yolk mass', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466272, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0142052', 'abnormal nasal region', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(466273, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100640', 'abnormal notochordal sheath', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(466274, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100702', 'abnormal glial cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(466275, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0141663', 'paralysed hindlimb', 0.4642857142857143, 5.504475013697824, 1.5986397697738417, 'HP:0040064', 'Abnormality of limbs'),
(466276, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0103626', 'abnormally increased number of hindlimb', 0.40625, 5.504475013697824, 1.4953905758412218, 'HP:0040064', 'Abnormality of limbs'),
(466277, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0125566', 'absent interdigital region', 0.4482758620689655, 5.504475013697824, 1.570835217966058, 'HP:0040064', 'Abnormality of limbs'),
(466278, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100484', 'abnormal cement gland primordium', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466279, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0131669', 'abnormal Roux spot', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(466280, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0107312', 'abnormal filopodium', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(466281, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100653', 'abnormal myoblast', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(466282, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100378', 'abnormal perichondrium', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(466283, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0101402', 'abnormal oropharyngeal papilla', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(466284, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100203', 'abnormal endocrine cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(466285, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0107271', 'abnormal apical region', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466286, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0115574', 'abnormal variability of size of hindlimb', 0.52, 5.504475013697824, 1.6918413067196547, 'HP:0040064', 'Abnormality of limbs'),
(466287, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100427', 'abnormal olfactory system', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(466288, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0101133', 'abnormal motor neuron', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(466289, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0101074', 'abnormal germinal vesicle', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(466290, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0101533', 'abnormal simple cuboidal epithelium', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466291, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0107272', 'abnormal axial region', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466292, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100721', 'abnormal centromere', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(466293, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100317', 'abnormal respiratory system', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(466294, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0101535', 'abnormal absorptive cell', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(466295, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0101072', 'abnormal mitochondrial cloud', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(466296, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100337', 'abnormal zygote', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(466297, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0131685', 'abnormal cortical actin cytoskeleton', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(466298, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100477', 'abnormal pericyte', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(466299, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0101424', 'abnormal coelomic epithelium', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466300, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100100', 'abnormal muscle', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(466301, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0141775', 'abnormal nitrogen compound metabolic process', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(466302, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0101460', 'abnormal fibrocellular pad', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466303, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100915', 'abnormal dermal system', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466304, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0101220', 'abnormal centriole', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(466305, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0101378', 'abnormal blastomere D1', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(466306, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100267', 'abnormal wound epidermis', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466307, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100187', 'abnormal regenerating limb', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466308, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100417', 'abnormal dense regular connective tissue', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(466309, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0131691', 'abnormal molecular function', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(466310, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0107273', 'abnormal basal region', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466311, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100742', 'abnormal musculoskeletal system', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466312, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100189', 'abnormal enteroendocrine cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(466313, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100509', 'abnormal germ plasm', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(466314, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100164', 'abnormal neural nucleus', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(466315, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0141792', 'abnormal small molecule metabolic process', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(466316, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100093', 'abnormal simple squamous epithelium', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466317, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0101518', 'abnormal B cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(466318, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100186', 'abnormal uveal tract', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466319, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0141272', 'absent surface breathing', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(466320, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0141784', 'abnormal cellular hormone metabolic process', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(466321, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0107284', 'abnormal migrating myoblast', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(466322, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0141787', 'abnormal hormone metabolic process', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(466323, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100727', 'abnormal odontogenic papilla', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(466324, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100605', 'abnormal prechordal plate', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466325, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100868', 'abnormal transporting epithelium', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466326, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100726', 'abnormal tail', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466327, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0101141', 'abnormal Keller explant', 0.5294117647058824, 1.706362323152461, 0.9504568842024205, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466328, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100258', 'abnormal organ part', 0.5294117647058824, 1.706362323152461, 0.9504568842024205, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466329, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100458', 'abnormal autopod', 0.5652173913043478, 5.504475013697824, 1.7638664937410224, 'HP:0040064', 'Abnormality of limbs'),
(466330, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0101187', 'abnormal dorsolateral commissural neuron', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(466331, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0141797', 'abnormal hydrogen metabolic process', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(466332, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0142051', 'abnormal cerebrospinal fluid', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(466333, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100665', 'abnormal egg jelly', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466334, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0101409', 'abnormal perivitelline space', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(466335, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100025', 'abnormal oocyte', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(466336, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0107263', 'abnormal anatomical side', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466337, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100449', 'abnormal lymphocyte', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(466338, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100152', 'abnormal alimentary system', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(466339, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0101503', 'abnormal organ cortex', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466340, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100201', 'abnormal cavitated compound organ', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466341, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100802', 'abnormal exocrine cell', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(466342, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100989', 'abnormal right blastomere', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(466343, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0102018', 'abnormal limb morphology', 0.40625, 5.504475013697824, 1.4953905758412218, 'HP:0040064', 'Abnormality of limbs'),
(466344, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0101326', 'abnormal cementoblast', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(466345, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0141795', 'abnormal glycosylation', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(466346, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0101513', 'abnormal basal body', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(466347, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0101461', 'abnormal sperm entry point', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(466348, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0101589', 'abnormal blastocoel roof', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466349, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0101297', 'abnormal barrier cell', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(466350, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0142056', 'abnormal main body axis', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466351, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0101168', 'abnormal circulating cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(466352, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0131687', 'abnormal astral microtubule', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(466353, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0101302', 'abnormal subcortical cytoplasm', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(466354, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0101543', 'abnormal external gill', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(466355, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0101132', 'abnormal apoptotic cell', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(466356, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100486', 'abnormal oral evagination', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(466357, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0141786', 'abnormal pigment metabolic process', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(466358, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0101577', 'abnormal notochordal epithelium', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466359, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100261', 'abnormal multilaminar epithelium', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466360, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100255', 'abnormal pelvic appendage', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466361, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0116434', 'abnormal biological process', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(466362, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100437', 'abnormal proepicardium', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(466363, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100273', 'abnormal visual system', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(466364, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0131667', 'abnormal actin cytoskeleton', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(466365, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100004', 'abnormal cell', 0.55, 1.8210412618256888, 1.0007860380741376, 'HP:0000118', 'Phenotypic abnormality'),
(466366, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100786', 'abnormal presumptive axial mesoderm', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466367, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0141796', 'abnormal demethylation', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(466368, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:00000000', 'Xenopus phenotype', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(466369, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100481', 'abnormal anatomical line', 0.5625, 1.706362323152461, 0.9797085315405084, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466370, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100917', 'abnormal stage III oocyte', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(466371, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100339', 'abnormal circumblastoporal collar', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466372, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100158', 'abnormal neuromere', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(466373, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0101110', 'abnormal cell-free extract', 0.5294117647058824, 1.706362323152461, 0.9504568842024205, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466374, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100531', 'abnormal proliferative region', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466375, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100890', 'abnormal pharyngeal cavity', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(466376, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100295', 'abnormal extracellular matrix', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466377, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0101406', 'abnormal cleavage furrow', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466378, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0107270', 'abnormal proximal-distal axis', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466379, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100296', 'abnormal tail region', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466380, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100899', 'abnormal secondary spermatogonium', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(466381, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100192', 'abnormal epithelium', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466382, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100549', 'abnormal mitotic cell', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(466383, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100172', 'abnormal stem cell', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(466384, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100392', 'abnormal cilium', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(466385, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0141263', 'abnormal visually guided collision avoidance behavior', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(466386, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100103', 'abnormal trunk', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466387, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100907', 'abnormal cytoplasm', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(466388, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100872', 'abnormal neuroendocrine cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(466389, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0101490', 'abnormal ectodermal cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(466390, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0115473', 'abnormally delayed phase of Mullerian duct', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(466391, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0101547', 'abnormal lampbrush chromosome', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(466392, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100376', 'abnormal animal pole', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466393, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0115391', 'abnormally undifferentiated alimentary system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(466394, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0107339', 'abnormal yolk platelet', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(466395, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100398', 'abnormal vegetal blastomere', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(466396, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0141745', 'abnormal creatinine homeostasis', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(466397, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0107285', 'abnormal flexural organ', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(466398, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0141266', 'abnormal surface breathing', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(466399, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100704', 'abnormal Merkel cell', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(466400, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100256', 'abnormal paired appendage', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466401, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100231', 'abnormal compound organ', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466402, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0101368', 'abnormal regenerating eye', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466403, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0141791', 'abnormal primary metabolic process', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(466404, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0141782', 'abnormal methylation', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(466405, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0115566', 'abnormal variability of size of forelimb', 0.52, 5.504475013697824, 1.6918413067196547, 'HP:0040064', 'Abnormality of limbs'),
(466406, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0101311', 'abnormal bottle cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(466407, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0101713', 'abnormal anatomical entity in vitro morphology', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466408, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100573', 'abnormal extraembryonic structure', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466409, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0141778', 'abnormal biosynthetic process', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(466410, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100285', 'abnormal progenitor cell', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(466411, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100612', 'abnormal unilaminar epithelium', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466412, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100059', 'abnormal regenerating tail', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466413, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100493', 'abnormal liver and biliary system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(466414, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100521', 'abnormal animal blastomere', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(466415, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0101263', 'abnormal blastocoel floor', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466416, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0101560', 'abnormal compound organ component', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466417, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0101463', 'abnormal right-ventral blastomere', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(466418, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0141777', 'abnormal catabolic process', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(466419, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0141771', 'abnormal urea homeostasis', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(466420, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0101389', 'abnormal wedge region', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(466421, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100510', 'abnormal forelimb stylopod', 0.48148148148148145, 5.504475013697824, 1.6279750564345348, 'HP:0040064', 'Abnormality of limbs'),
(466422, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100070', 'abnormal anatomical system', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466423, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0131729', 'abnormal regulation of growth rate', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(466424, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100642', 'abnormal gustatory system', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(466425, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0141715', 'abnormal septum', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466426, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0141904', 'abnormal glucosamine metabolic process', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(466427, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100006', 'abnormal anatomical structure', 0.5625, 1.706362323152461, 0.9797085315405084, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466428, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0107266', 'abnormal dorsal side', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466429, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0141718', 'abnormal posterior notochord', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(466430, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100707', 'abnormal central vegetal yolk mass', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466431, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100898', 'abnormal hindlimb stylopod', 0.48148148148148145, 5.504475013697824, 1.6279750564345348, 'HP:0040064', 'Abnormality of limbs'),
(466432, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0101010', 'abnormal dorsal marginal zone', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466433, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0101497', 'abnormal ciliary axoneme', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(466434, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100307', 'abnormal blastomere', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(466435, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100969', 'abnormal disaggregated/reaggregated ectoderm treated with activin', 0.5294117647058824, 1.706362323152461, 0.9504568842024205, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466436, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0101098', 'abnormal mineralized extracellular matrix', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466437, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0141860', 'abnormal malate-aspartate shuttle', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(466438, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0101149', 'abnormal amputated limb', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466439, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0115758', 'abnormally decreased mobility of melanoblast', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(466440, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0101468', 'abnormal stage I oocyte', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(466441, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0115509', 'abnormally semi-viable whole organism', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466442, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100501', 'abnormal urogenital system', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(466443, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0141600', 'absent metamorphosis', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(466444, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0101004', 'abnormal acid secreting cell', 0.5238095238095238, 1.8210412618256888, 0.9766671675624242, 'HP:0000118', 'Phenotypic abnormality'),
(466445, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0131725', 'abnormal phosphorylation of RNA polymerase II C-terminal domain', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(466446, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100207', 'abnormal blastema', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466447, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0141662', 'paralysed forelimb', 0.4642857142857143, 5.504475013697824, 1.5986397697738417, 'HP:0040064', 'Abnormality of limbs'),
(466448, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0101061', 'abnormal plasma membrane', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(466449, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0101057', 'abnormal vegetal pole', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466450, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100232', 'abnormal lymphatic system', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(466451, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0128000', 'absent behavior', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(466452, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0101029', 'abnormal right spleen primordium', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(466453, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100574', 'abnormal gastrula cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(466454, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0115362', 'abnormally decreased adhesivity of prechordal plate', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466455, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100626', 'abnormal primordial germ cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(466456, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0107265', 'abnormal posterior side', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466457, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100581', 'abnormal immune system', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(466458, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100069', 'abnormal urinary system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(466459, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100383', 'abnormal amputated fin', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466460, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0141809', 'abnormal catalytic activity', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(466461, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100976', 'abnormal multiciliated cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(466462, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100433', 'abnormal pectoral appendage', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466463, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0107288', 'abnormal larval alimentary system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(466464, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100010', 'abnormal multicellular anatomical structure', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466465, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0101040', 'abnormal axial mesoderm', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466466, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0126540', 'abnormally localised limb segment', 0.41935483870967744, 5.504475013697824, 1.5193183443737854, 'HP:0040064', 'Abnormality of limbs'),
(466467, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0101553', 'abnormal dental epithelium', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466468, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0101174', 'abnormal articular system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(466469, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0141497', 'abnormal lymphoblast', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(466470, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100422', 'abnormal notochord', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(466471, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0115508', 'abnormally peramorphic growth of whole organism', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466472, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100268', 'abnormal circulatory system', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466473, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0115505', 'dead whole organism', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466474, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100332', 'abnormal germinal granule', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(466475, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0141276', 'decreased surface breathing', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(466476, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100104', 'abnormal embryonic structure', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466477, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0107311', 'abnormal apical junction complex', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(466478, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100003', 'abnormal organism subdivision', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(466479, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100784', 'abnormal left blastomere', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(466480, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100745', 'abnormal anterior lymph sac', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(466481, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0127203', 'abnormally localised interdigital region', 0.48148148148148145, 5.504475013697824, 1.6279750564345348, 'HP:0040064', 'Abnormality of limbs'),
(466482, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100242', 'abnormal right lymph heart', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(466483, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100402', 'abnormal zeugopod', 0.5652173913043478, 5.504475013697824, 1.7638664937410224, 'HP:0040064', 'Abnormality of limbs'),
(466484, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100687', 'abnormal periotic region', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(466485, 'HP:0002814', 'Abnormality of the lower limb', 'XPO:0100846', 'abnormal hindlimb', 0.5416666666666666, 5.504475013697824, 1.7267283030111178, 'HP:0040064', 'Abnormality of limbs'),
(466486, 'HP:0003704', 'Scapuloperoneal weakness', 'XPO:0100100', 'abnormal muscle', 0.42424242424242425, 5.968280811662945, 1.591225288920281, 'UPHENO:0002816', 'abnormal musculature'),
(466487, 'HP:0003704', 'Scapuloperoneal weakness', 'XPO:0100746', 'abnormal smooth muscle', 0.4117647058823529, 5.968280811662945, 1.5676502776568768, 'UPHENO:0002816', 'abnormal musculature'),
(466488, 'HP:0003704', 'Scapuloperoneal weakness', 'XPO:0100275', 'abnormal skeletal muscle', 0.4117647058823529, 5.968280811662945, 1.5676502776568768, 'UPHENO:0002816', 'abnormal musculature'),
(466489, 'HP:0008589', 'Hypoplastic helices', 'XPO:0129311', 'decreased size of the lateral nasal prominence', 0.4067796610169492, 5.653868323764771, 1.5165350771332327, 'UPHENO:0012541', 'decreased size of the anatomical entity in the independent continuant'),
(466490, 'HP:0008589', 'Hypoplastic helices', 'XPO:0103358', 'decreased size of the pharyngeal region', 0.4444444444444444, 5.653868323764771, 1.5851909557266834, 'UPHENO:0012541', 'decreased size of the anatomical entity in the independent continuant'),
(466491, 'HP:0008589', 'Hypoplastic helices', 'XPO:0131600', 'decreased size of the intercanthal region', 0.42105263157894735, 5.653868323764771, 1.5429115776096853, 'UPHENO:0012541', 'decreased size of the anatomical entity in the independent continuant'),
(466492, 'HP:0008589', 'Hypoplastic helices', 'XPO:0128582', 'decreased size of the head region', 0.42105263157894735, 5.653868323764771, 1.5429115776096853, 'UPHENO:0012541', 'decreased size of the anatomical entity in the independent continuant'),
(466493, 'HP:0008589', 'Hypoplastic helices', 'XPO:0103342', 'decreased size of the head', 0.4067796610169492, 5.653868323764771, 1.5165350771332327, 'UPHENO:0012541', 'decreased size of the anatomical entity in the independent continuant'),
(466494, 'HP:0008589', 'Hypoplastic helices', 'XPO:0129164', 'decreased size of the medial nasal prominence', 0.4067796610169492, 5.653868323764771, 1.5165350771332327, 'UPHENO:0012541', 'decreased size of the anatomical entity in the independent continuant'),
(466495, 'HP:0008589', 'Hypoplastic helices', 'XPO:0126939', 'abnormally localised auditory apparatus', 0.4782608695652174, 10.484129389061598, 2.2392295188852014, 'UPHENO:0005986', 'abnormal shape of external ear'),
(466496, 'HP:0008589', 'Hypoplastic helices', 'XPO:0102259', 'abnormal pharyngeal region morphology', 0.40384615384615385, 4.5318002188002176, 1.3528303989641963, 'UPHENO:0087907', 'abnormal head morphology'),
(466497, 'HP:0003282', 'Low alkaline phosphatase', 'XPO:0141777', 'abnormal catabolic process', 0.4074074074074074, 4.758907843651163, 1.392413123563799, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(466498, 'HP:0003282', 'Low alkaline phosphatase', 'XPO:0141791', 'abnormal primary metabolic process', 0.4074074074074074, 4.758907843651163, 1.392413123563799, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(466499, 'HP:0003282', 'Low alkaline phosphatase', 'XPO:0141775', 'abnormal nitrogen compound metabolic process', 0.4074074074074074, 4.758907843651163, 1.392413123563799, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(466500, 'HP:0003282', 'Low alkaline phosphatase', 'XPO:0141786', 'abnormal pigment metabolic process', 0.4074074074074074, 4.758907843651163, 1.392413123563799, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(466501, 'HP:0003282', 'Low alkaline phosphatase', 'XPO:0141797', 'abnormal hydrogen metabolic process', 0.4074074074074074, 4.758907843651163, 1.392413123563799, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(466502, 'HP:0003282', 'Low alkaline phosphatase', 'XPO:0141776', 'abnormal metabolic process', 0.44, 4.758907843651163, 1.447038165082909, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(466503, 'HP:0003282', 'Low alkaline phosphatase', 'XPO:0141796', 'abnormal demethylation', 0.4074074074074074, 4.758907843651163, 1.392413123563799, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(466504, 'HP:0003282', 'Low alkaline phosphatase', 'XPO:0141781', 'abnormal secondary metabolic process', 0.4074074074074074, 4.758907843651163, 1.392413123563799, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(466505, 'HP:0003282', 'Low alkaline phosphatase', 'XPO:0141792', 'abnormal small molecule metabolic process', 0.4074074074074074, 4.758907843651163, 1.392413123563799, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(466506, 'HP:0003282', 'Low alkaline phosphatase', 'XPO:0141794', 'abnormal prosthetic group metabolic process', 0.4074074074074074, 4.758907843651163, 1.392413123563799, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(466507, 'HP:0003282', 'Low alkaline phosphatase', 'XPO:0141778', 'abnormal biosynthetic process', 0.4074074074074074, 4.758907843651163, 1.392413123563799, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(466508, 'HP:0003282', 'Low alkaline phosphatase', 'XPO:0141904', 'abnormal glucosamine metabolic process', 0.4074074074074074, 4.758907843651163, 1.392413123563799, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(466509, 'HP:0003282', 'Low alkaline phosphatase', 'XPO:0141787', 'abnormal hormone metabolic process', 0.4074074074074074, 4.758907843651163, 1.392413123563799, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(466510, 'HP:0003282', 'Low alkaline phosphatase', 'XPO:0141783', 'abnormal collagen metabolic process', 0.4074074074074074, 4.758907843651163, 1.392413123563799, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(466511, 'HP:0003282', 'Low alkaline phosphatase', 'XPO:0141782', 'abnormal methylation', 0.4074074074074074, 4.758907843651163, 1.392413123563799, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(466512, 'HP:0008231', 'Macronodular adrenal hyperplasia', 'XPO:0129788', 'increased size of the organ part', 0.41025641025641024, 5.972749669260594, 1.565362206861726, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(466513, 'HP:0008231', 'Macronodular adrenal hyperplasia', 'XPO:0129735', 'increased size of the endocrine system', 0.4782608695652174, 7.428233084304616, 1.884843021111478, 'UPHENO:0076812', 'abnormal endocrine system morphology'),
(466514, 'HP:0008231', 'Macronodular adrenal hyperplasia', 'XPO:0130297', 'increased size of the adrenal gland', 0.5636363636363636, 15.404694921567193, 2.946633032550828, 'HP:0008221', 'Adrenal hyperplasia'),
(466515, 'HP:0008231', 'Macronodular adrenal hyperplasia', 'XPO:0129582', 'increased size of the portion of organism substance', 0.4444444444444444, 5.972749669260594, 1.629280641436663, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(466516, 'HP:0008231', 'Macronodular adrenal hyperplasia', 'XPO:0101835', 'abnormal endocrine cell morphology', 0.40425531914893614, 7.428233084304616, 1.7328885527373792, 'UPHENO:0076812', 'abnormal endocrine system morphology'),
(466517, 'HP:0008231', 'Macronodular adrenal hyperplasia', 'XPO:0129076', 'decreased size of the adrenal medulla', 0.4098360655737705, 11.30515924801628, 2.1525013326109503, 'UPHENO:0087384', 'abnormal adrenal gland morphology'),
(466518, 'HP:0008231', 'Macronodular adrenal hyperplasia', 'XPO:0130595', 'increased size of the postero-dorsal region', 0.41025641025641024, 5.972749669260594, 1.565362206861726, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(466519, 'HP:0008231', 'Macronodular adrenal hyperplasia', 'XPO:0129988', 'increased size of the dorso-lateral region', 0.41025641025641024, 5.972749669260594, 1.565362206861726, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(466520, 'HP:0008231', 'Macronodular adrenal hyperplasia', 'XPO:0102722', 'abnormal adrenal gland morphology', 0.5306122448979592, 11.7363164126584, 2.495482558254703, 'UPHENO:0020671', 'abnormal adrenal gland morphology'),
(466521, 'HP:0008231', 'Macronodular adrenal hyperplasia', 'XPO:0130553', 'increased size of the adrenal medulla', 0.45, 11.30515924801628, 2.255509180120384, 'UPHENO:0087384', 'abnormal adrenal gland morphology'),
(466522, 'HP:0008231', 'Macronodular adrenal hyperplasia', 'XPO:0125656', 'absent adrenal gland', 0.4262295081967213, 11.7363164126584, 2.2365966048012544, 'UPHENO:0020671', 'abnormal adrenal gland morphology'),
(466523, 'HP:0008231', 'Macronodular adrenal hyperplasia', 'XPO:0102492', 'abnormal parathyroid morphology', 0.42857142857142855, 7.767034997756375, 1.8244805520346694, 'UPHENO:0087376', 'abnormal endocrine gland morphology'),
(466524, 'HP:0008231', 'Macronodular adrenal hyperplasia', 'XPO:0102388', 'abnormal adrenal medulla morphology', 0.4528301886792453, 11.30515924801628, 2.2625908590216053, 'UPHENO:0087384', 'abnormal adrenal gland morphology'),
(466525, 'HP:0008231', 'Macronodular adrenal hyperplasia', 'XPO:0129733', 'increased size of the ultimobranchial body', 0.48, 7.767034997756375, 1.93084872502303, 'UPHENO:0087376', 'abnormal endocrine gland morphology'),
(466526, 'HP:0008231', 'Macronodular adrenal hyperplasia', 'XPO:0130623', 'increased size of the ventro-lateral region', 0.41025641025641024, 5.972749669260594, 1.565362206861726, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(466527, 'HP:0008231', 'Macronodular adrenal hyperplasia', 'XPO:0130552', 'increased size of the ventral region', 0.41025641025641024, 5.972749669260594, 1.565362206861726, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(466528, 'HP:0008231', 'Macronodular adrenal hyperplasia', 'XPO:0140281', 'abnormally necrotic endocrine system', 0.40425531914893614, 7.428233084304616, 1.7328885527373792, 'UPHENO:0076812', 'abnormal endocrine system morphology'),
(466529, 'HP:0008231', 'Macronodular adrenal hyperplasia', 'XPO:0128819', 'decreased size of the adrenal gland', 0.46551724137931033, 11.7363164126584, 2.337404038752278, 'UPHENO:0020671', 'abnormal adrenal gland morphology'),
(466530, 'HP:0008231', 'Macronodular adrenal hyperplasia', 'XPO:0130304', 'increased size of the parathyroid', 0.4444444444444444, 7.767034997756375, 1.8579600519274866, 'UPHENO:0087376', 'abnormal endocrine gland morphology'),
(466531, 'HP:0008231', 'Macronodular adrenal hyperplasia', 'XPO:0129551', 'increased size of the cell part', 0.4186046511627907, 5.972749669260594, 1.5812086490351311, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(466532, 'HP:0008231', 'Macronodular adrenal hyperplasia', 'XPO:0140100', 'abnormally necrotic adrenal cortex', 0.45614035087719296, 11.7363164126584, 2.313743176429865, 'UPHENO:0020671', 'abnormal adrenal gland morphology'),
(466533, 'HP:0008231', 'Macronodular adrenal hyperplasia', 'XPO:0130865', 'increased size of the antero-dorsal region', 0.41025641025641024, 5.972749669260594, 1.565362206861726, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(466534, 'HP:0008231', 'Macronodular adrenal hyperplasia', 'XPO:0128454', 'decreased size of the adrenal cortex', 0.46551724137931033, 11.7363164126584, 2.337404038752278, 'UPHENO:0020671', 'abnormal adrenal gland morphology'),
(466535, 'HP:0008231', 'Macronodular adrenal hyperplasia', 'XPO:0129982', 'increased size of the anatomical line', 0.4444444444444444, 5.972749669260594, 1.629280641436663, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(466536, 'HP:0008231', 'Macronodular adrenal hyperplasia', 'XPO:0101857', 'abnormal endocrine system morphology', 0.4523809523809524, 7.428233084304616, 1.8331369717469073, 'UPHENO:0076812', 'abnormal endocrine system morphology'),
(466537, 'HP:0008231', 'Macronodular adrenal hyperplasia', 'XPO:0102472', 'abnormal thyroid morphology', 0.4117647058823529, 7.767034997756375, 1.7883486464974037, 'UPHENO:0087376', 'abnormal endocrine gland morphology'),
(466538, 'HP:0008231', 'Macronodular adrenal hyperplasia', 'XPO:0129487', 'increased size of the anatomical structure', 0.4444444444444444, 5.972749669260594, 1.629280641436663, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(466539, 'HP:0008231', 'Macronodular adrenal hyperplasia', 'XPO:0127939', 'abnormally localised adrenal cortex', 0.4642857142857143, 11.7363164126584, 2.33431018691481, 'UPHENO:0020671', 'abnormal adrenal gland morphology'),
(466540, 'HP:0008231', 'Macronodular adrenal hyperplasia', 'XPO:0101561', 'abnormal adrenal cortex', 0.5531914893617021, 11.7363164126584, 2.548024795000765, 'UPHENO:0020671', 'abnormal adrenal gland morphology'),
(466541, 'HP:0008231', 'Macronodular adrenal hyperplasia', 'XPO:0129934', 'increased size of the adrenal cortex', 0.5178571428571429, 11.7363164126584, 2.4653063268337814, 'UPHENO:0020671', 'abnormal adrenal gland morphology'),
(466542, 'HP:0008231', 'Macronodular adrenal hyperplasia', 'XPO:0128253', 'decreased size of the ultimobranchial body', 0.4230769230769231, 7.767034997756375, 1.81274743642945, 'UPHENO:0087376', 'abnormal endocrine gland morphology'),
(466543, 'HP:0008231', 'Macronodular adrenal hyperplasia', 'XPO:0130532', 'increased size of the thyroid', 0.41379310344827586, 7.767034997756375, 1.7927480348094047, 'UPHENO:0087376', 'abnormal endocrine gland morphology'),
(466544, 'HP:0008231', 'Macronodular adrenal hyperplasia', 'XPO:0128255', 'decreased size of the endocrine system', 0.4166666666666667, 7.428233084304616, 1.7592888104175097, 'UPHENO:0076812', 'abnormal endocrine system morphology'),
(466545, 'HP:0008231', 'Macronodular adrenal hyperplasia', 'XPO:0140682', 'abnormally necrotic adrenal gland', 0.4642857142857143, 11.7363164126584, 2.33431018691481, 'UPHENO:0020671', 'abnormal adrenal gland morphology'),
(466546, 'HP:0008231', 'Macronodular adrenal hyperplasia', 'XPO:0139937', 'abnormally necrotic ultimobranchial body', 0.4117647058823529, 7.767034997756375, 1.7883486464974037, 'UPHENO:0087376', 'abnormal endocrine gland morphology'),
(466547, 'HP:0008231', 'Macronodular adrenal hyperplasia', 'XPO:0103193', 'abnormal adrenal cortex morphology', 0.5, 11.7363164126584, 2.422428163295911, 'UPHENO:0020671', 'abnormal adrenal gland morphology'),
(466548, 'HP:0008231', 'Macronodular adrenal hyperplasia', 'XPO:0130401', 'increased size of the posterior region', 0.41025641025641024, 5.972749669260594, 1.565362206861726, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(466549, 'HP:0008231', 'Macronodular adrenal hyperplasia', 'XPO:0129571', 'increased size of the anatomical region', 0.42105263157894735, 5.972749669260594, 1.585825326448175, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(466550, 'HP:0008231', 'Macronodular adrenal hyperplasia', 'XPO:0129517', 'increased size of the anatomical space', 0.42105263157894735, 5.972749669260594, 1.585825326448175, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(466551, 'HP:0008231', 'Macronodular adrenal hyperplasia', 'XPO:0102655', 'abnormal ultimobranchial body morphology', 0.45652173913043476, 7.767034997756375, 1.8830348709099076, 'UPHENO:0087376', 'abnormal endocrine gland morphology'),
(466552, 'HP:0008231', 'Macronodular adrenal hyperplasia', 'XPO:0126275', 'absent adrenal cortex', 0.4406779661016949, 11.7363164126584, 2.274189096415741, 'UPHENO:0020671', 'abnormal adrenal gland morphology'),
(466553, 'HP:0100257', 'Ectrodactyly', 'XPO:0103839', 'abnormally decreased number of digit-joint region in the regenerating hindlimb', 0.4482758620689655, 5.802924133159483, 1.6128579659451951, 'UPHENO:0076727', 'abnormal limb bone morphology'),
(466554, 'HP:0100257', 'Ectrodactyly', 'XPO:0103833', 'abnormally decreased number of digit-joint region in the regenerating forelimb', 0.4482758620689655, 5.802924133159483, 1.6128579659451951, 'UPHENO:0076727', 'abnormal limb bone morphology'),
(466555, 'HP:0100257', 'Ectrodactyly', 'XPO:0125443', 'absent digit-joint region', 0.48148148148148145, 5.802924133159483, 1.6715264007960717, 'UPHENO:0076727', 'abnormal limb bone morphology'),
(466556, 'HP:0100257', 'Ectrodactyly', 'XPO:0141568', 'abnormal digit-joint region morphology in the regenerating forelimb', 0.4406779661016949, 5.802924133159483, 1.5991312655448777, 'UPHENO:0076727', 'abnormal limb bone morphology'),
(466557, 'HP:0100257', 'Ectrodactyly', 'XPO:0129693', 'increased size of the digit', 0.41935483870967744, 5.802924133159483, 1.5599629206829213, 'UPHENO:0076727', 'abnormal limb bone morphology'),
(466558, 'HP:0100257', 'Ectrodactyly', 'XPO:0102806', 'abnormal articular system morphology', 0.40476190476190477, 4.638757693672553, 1.3702526773627712, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(466559, 'HP:0100257', 'Ectrodactyly', 'XPO:0102217', 'abnormal elastica externa morphology', 0.4146341463414634, 4.638757693672553, 1.3868624071625903, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(466560, 'HP:0100257', 'Ectrodactyly', 'XPO:0101114', 'abnormal forelimb digit 2', 0.4482758620689655, 5.802924133159483, 1.6128579659451951, 'UPHENO:0076727', 'abnormal limb bone morphology'),
(466561, 'HP:0100257', 'Ectrodactyly', 'XPO:0100852', 'abnormal interdigital region', 0.40625, 5.504475013697824, 1.4953905758412218, 'HP:0040064', 'Abnormality of limbs'),
(466562, 'HP:0100257', 'Ectrodactyly', 'XPO:0100178', 'abnormal digit', 0.6341463414634146, 5.802924133159483, 1.9183073551526728, 'UPHENO:0076727', 'abnormal limb bone morphology'),
(466563, 'HP:0100257', 'Ectrodactyly', 'XPO:0100582', 'abnormal forelimb digit', 0.45614035087719296, 5.802924133159483, 1.6269443291683638, 'UPHENO:0076727', 'abnormal limb bone morphology'),
(466564, 'HP:0100257', 'Ectrodactyly', 'XPO:0100177', 'abnormal hindlimb digit', 0.49056603773584906, 5.802924133159483, 1.6872218287130427, 'UPHENO:0076727', 'abnormal limb bone morphology'),
(466565, 'HP:0100257', 'Ectrodactyly', 'XPO:0101810', 'abnormal digit morphology', 0.49056603773584906, 5.802924133159483, 1.6872218287130427, 'UPHENO:0076727', 'abnormal limb bone morphology'),
(466566, 'HP:0100257', 'Ectrodactyly', 'XPO:0103618', 'abnormal number of hindlimb digit 5', 0.4406779661016949, 5.802924133159483, 1.5991312655448777, 'UPHENO:0076727', 'abnormal limb bone morphology'),
(466567, 'HP:0100257', 'Ectrodactyly', 'XPO:0103616', 'abnormal number of hindlimb digit 3', 0.4406779661016949, 5.802924133159483, 1.5991312655448777, 'UPHENO:0076727', 'abnormal limb bone morphology'),
(466568, 'HP:0100257', 'Ectrodactyly', 'XPO:0100934', 'abnormal claw primordium', 0.4727272727272727, 5.802924133159483, 1.6562609997557014, 'UPHENO:0076727', 'abnormal limb bone morphology'),
(466569, 'HP:0100257', 'Ectrodactyly', 'XPO:0103632', 'abnormally increased number of digit', 0.49056603773584906, 5.802924133159483, 1.6872218287130427, 'UPHENO:0076727', 'abnormal limb bone morphology'),
(466570, 'HP:0100257', 'Ectrodactyly', 'XPO:0101248', 'abnormal digit-joint region', 0.5909090909090909, 5.802924133159483, 1.8517560919677556, 'UPHENO:0076727', 'abnormal limb bone morphology'),
(466571, 'HP:0100257', 'Ectrodactyly', 'XPO:0102880', 'abnormal digit-joint region morphology', 0.49056603773584906, 5.802924133159483, 1.6872218287130427, 'UPHENO:0076727', 'abnormal limb bone morphology'),
(466572, 'HP:0100257', 'Ectrodactyly', 'XPO:0128213', 'decreased size of the digit', 0.41935483870967744, 5.802924133159483, 1.5599629206829213, 'UPHENO:0076727', 'abnormal limb bone morphology'),
(466573, 'HP:0100257', 'Ectrodactyly', 'XPO:0103622', 'abnormal number of forelimb digit 5', 0.4126984126984127, 5.802924133159483, 1.547532739157473, 'UPHENO:0076727', 'abnormal limb bone morphology'),
(466574, 'HP:0100257', 'Ectrodactyly', 'XPO:0129977', 'increased size of the digit-joint region', 0.4406779661016949, 5.802924133159483, 1.5991312655448777, 'UPHENO:0076727', 'abnormal limb bone morphology'),
(466575, 'HP:0100257', 'Ectrodactyly', 'XPO:0103613', 'abnormal number of hindlimb digits', 0.45614035087719296, 5.802924133159483, 1.6269443291683638, 'UPHENO:0076727', 'abnormal limb bone morphology'),
(466576, 'HP:0100257', 'Ectrodactyly', 'XPO:0103619', 'abnormal number of forelimb digit 2', 0.4126984126984127, 5.802924133159483, 1.547532739157473, 'UPHENO:0076727', 'abnormal limb bone morphology'),
(466577, 'HP:0100257', 'Ectrodactyly', 'XPO:0124986', 'absent digit', 0.4727272727272727, 5.802924133159483, 1.6562609997557014, 'UPHENO:0076727', 'abnormal limb bone morphology'),
(466578, 'HP:0100257', 'Ectrodactyly', 'XPO:0103620', 'abnormal number of forelimb digit 3', 0.4126984126984127, 5.802924133159483, 1.547532739157473, 'UPHENO:0076727', 'abnormal limb bone morphology'),
(466579, 'HP:0100257', 'Ectrodactyly', 'XPO:0101316', 'abnormal hindlimb digit 5', 0.48148148148148145, 5.802924133159483, 1.6715264007960717, 'UPHENO:0076727', 'abnormal limb bone morphology'),
(466580, 'HP:0100257', 'Ectrodactyly', 'XPO:0103621', 'abnormal number of forelimb digit 4', 0.4126984126984127, 5.802924133159483, 1.547532739157473, 'UPHENO:0076727', 'abnormal limb bone morphology'),
(466581, 'HP:0100257', 'Ectrodactyly', 'XPO:0101244', 'abnormal hindlimb digit 4', 0.48148148148148145, 5.802924133159483, 1.6715264007960717, 'UPHENO:0076727', 'abnormal limb bone morphology'),
(466582, 'HP:0100257', 'Ectrodactyly', 'XPO:0100240', 'abnormal hindlimb digit 1', 0.48148148148148145, 5.802924133159483, 1.6715264007960717, 'UPHENO:0076727', 'abnormal limb bone morphology'),
(466583, 'HP:0100257', 'Ectrodactyly', 'XPO:0126603', 'abnormally localised digit', 0.49056603773584906, 5.802924133159483, 1.6872218287130427, 'UPHENO:0076727', 'abnormal limb bone morphology'),
(466584, 'HP:0100257', 'Ectrodactyly', 'XPO:0100585', 'abnormal elastica externa', 0.42424242424242425, 4.3395673355180735, 1.3568450783281876, 'UPHENO:0002964', 'abnormal skeletal system'),
(466585, 'HP:0100257', 'Ectrodactyly', 'XPO:0127078', 'abnormally localised digit-joint region', 0.5, 5.802924133159483, 1.7033678600289903, 'UPHENO:0076727', 'abnormal limb bone morphology'),
(466586, 'HP:0100257', 'Ectrodactyly', 'XPO:0100897', 'abnormal forelimb digit 4', 0.4482758620689655, 5.802924133159483, 1.6128579659451951, 'UPHENO:0076727', 'abnormal limb bone morphology'),
(466587, 'HP:0100257', 'Ectrodactyly', 'XPO:0103611', 'abnormal number of forelimb digits', 0.4262295081967213, 5.802924133159483, 1.5726975231682194, 'UPHENO:0076727', 'abnormal limb bone morphology'),
(466588, 'HP:0100257', 'Ectrodactyly', 'XPO:0103614', 'abnormal number of hindlimb digit 1', 0.4406779661016949, 5.802924133159483, 1.5991312655448777, 'UPHENO:0076727', 'abnormal limb bone morphology'),
(466589, 'HP:0100257', 'Ectrodactyly', 'XPO:0141208', 'abnormally necrotic digit-joint region', 0.45614035087719296, 5.802924133159483, 1.6269443291683638, 'UPHENO:0076727', 'abnormal limb bone morphology'),
(466590, 'HP:0100257', 'Ectrodactyly', 'XPO:0141569', 'abnormal digit-joint region morphology in the regenerating hindlimb', 0.4406779661016949, 5.802924133159483, 1.5991312655448777, 'UPHENO:0076727', 'abnormal limb bone morphology'),
(466591, 'HP:0100257', 'Ectrodactyly', 'XPO:0100465', 'abnormal skeletal system', 0.4117647058823529, 4.3395673355180735, 1.3367425584480601, 'UPHENO:0002964', 'abnormal skeletal system'),
(466592, 'HP:0100257', 'Ectrodactyly', 'XPO:0100548', 'abnormal hindlimb digit 3', 0.48148148148148145, 5.802924133159483, 1.6715264007960717, 'UPHENO:0076727', 'abnormal limb bone morphology'),
(466593, 'HP:0100257', 'Ectrodactyly', 'XPO:0100422', 'abnormal notochord', 0.4117647058823529, 4.3395673355180735, 1.3367425584480601, 'UPHENO:0002964', 'abnormal skeletal system'),
(466594, 'HP:0100257', 'Ectrodactyly', 'XPO:0100419', 'abnormal hindlimb digit 2', 0.48148148148148145, 5.802924133159483, 1.6715264007960717, 'UPHENO:0076727', 'abnormal limb bone morphology'),
(466595, 'HP:0100257', 'Ectrodactyly', 'XPO:0102097', 'abnormal skeletal system morphology', 0.4146341463414634, 4.638757693672553, 1.3868624071625903, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(466596, 'HP:0100257', 'Ectrodactyly', 'XPO:0103615', 'abnormal number of hindlimb digit 2', 0.4406779661016949, 5.802924133159483, 1.5991312655448777, 'UPHENO:0076727', 'abnormal limb bone morphology'),
(466597, 'HP:0100257', 'Ectrodactyly', 'XPO:0101155', 'abnormal forelimb digit 5', 0.4482758620689655, 5.802924133159483, 1.6128579659451951, 'UPHENO:0076727', 'abnormal limb bone morphology'),
(466598, 'HP:0100257', 'Ectrodactyly', 'XPO:0100966', 'abnormal forelimb digit 3', 0.4482758620689655, 5.802924133159483, 1.6128579659451951, 'UPHENO:0076727', 'abnormal limb bone morphology'),
(466599, 'HP:0100257', 'Ectrodactyly', 'XPO:0139962', 'abnormally necrotic digit', 0.43333333333333335, 5.802924133159483, 1.5857491786857223, 'UPHENO:0076727', 'abnormal limb bone morphology'),
(466600, 'HP:0100257', 'Ectrodactyly', 'XPO:0101982', 'abnormal appendicular skeleton morphology', 0.41304347826086957, 5.732269579595698, 1.5387256303464825, 'HP:0011844', 'Abnormal appendicular skeleton morphology'),
(466601, 'HP:0100257', 'Ectrodactyly', 'XPO:0128497', 'decreased size of the digit-joint region', 0.4406779661016949, 5.802924133159483, 1.5991312655448777, 'UPHENO:0076727', 'abnormal limb bone morphology'),
(466602, 'HP:0100257', 'Ectrodactyly', 'XPO:0103617', 'abnormal number of hindlimb digit 4', 0.4406779661016949, 5.802924133159483, 1.5991312655448777, 'UPHENO:0076727', 'abnormal limb bone morphology'),
(466603, 'HP:0010468', 'Aplasia/Hypoplasia of the testes', 'XPO:0139754', 'abnormally necrotic testis', 0.6814159292035398, 10.7042552034261, 2.7007498969498123, 'HP:0000035', 'Abnormal testis morphology'),
(466604, 'HP:0010468', 'Aplasia/Hypoplasia of the testes', 'XPO:0102046', 'abnormal testis morphology', 0.7333333333333333, 10.7042552034261, 2.8017471601090524, 'HP:0000035', 'Abnormal testis morphology'),
(466605, 'HP:0010468', 'Aplasia/Hypoplasia of the testes', 'XPO:0130039', 'increased size of the testis', 0.6610169491525424, 11.872199840740173, 2.801379181484607, 'HP:0045058', 'Abnormality of the testis size'),
(466606, 'HP:0010468', 'Aplasia/Hypoplasia of the testes', 'XPO:0130391', 'increased size of the seminiferous tubule', 0.65, 11.872199840740173, 2.7779362657341715, 'HP:0045058', 'Abnormality of the testis size'),
(466607, 'HP:0010468', 'Aplasia/Hypoplasia of the testes', 'XPO:0128913', 'decreased size of the seminiferous tubule', 0.6554621848739496, 11.872199840740173, 2.7895838483314512, 'HP:0045058', 'Abnormality of the testis size'),
(466608, 'HP:0010468', 'Aplasia/Hypoplasia of the testes', 'XPO:0128559', 'decreased size of the testis', 0.6220472440944882, 13.7526182249875, 2.9248552555531884, 'HP:0010468', 'Aplasia/Hypoplasia of the testes'),
(466609, 'HP:0031668', 'Diastolic heart murmur', 'XPO:0100076', 'abnormal artery', 0.4117647058823529, 5.249153838287537, 1.4701755971154233, 'UPHENO:0080362', 'abnormal cardiovascular system'),
(466610, 'HP:0031668', 'Diastolic heart murmur', 'XPO:0100780', 'abnormal vascular plexus', 0.4117647058823529, 5.249153838287537, 1.4701755971154233, 'UPHENO:0080362', 'abnormal cardiovascular system'),
(466611, 'HP:0031668', 'Diastolic heart murmur', 'XPO:0100043', 'abnormal vein', 0.4117647058823529, 5.249153838287537, 1.4701755971154233, 'UPHENO:0080362', 'abnormal cardiovascular system'),
(466612, 'HP:0031668', 'Diastolic heart murmur', 'XPO:0100054', 'abnormal blood vessel', 0.42424242424242425, 5.249153838287537, 1.4922847414540332, 'UPHENO:0080362', 'abnormal cardiovascular system'),
(466613, 'HP:0031668', 'Diastolic heart murmur', 'XPO:0100004', 'abnormal cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(466614, 'HP:0031668', 'Diastolic heart murmur', 'XPO:0101583', 'abnormal truncus arteriosus', 0.4117647058823529, 5.249153838287537, 1.4701755971154233, 'UPHENO:0080362', 'abnormal cardiovascular system'),
(466615, 'HP:0031668', 'Diastolic heart murmur', 'XPO:0100981', 'abnormal dorsal longitudinal anastomosing vessel', 0.4117647058823529, 5.249153838287537, 1.4701755971154233, 'UPHENO:0080362', 'abnormal cardiovascular system'),
(466616, 'HP:0031668', 'Diastolic heart murmur', 'XPO:0100792', 'abnormal capillary', 0.4117647058823529, 5.249153838287537, 1.4701755971154233, 'UPHENO:0080362', 'abnormal cardiovascular system'),
(466617, 'HP:0008290', 'Partial complement factor H deficiency', 'XPO:0100745', 'abnormal anterior lymph sac', 0.40625, 5.64885357140806, 1.5148751642906173, 'HP:0002715', 'Abnormality of the immune system'),
(466618, 'HP:0008290', 'Partial complement factor H deficiency', 'XPO:0101451', 'abnormal dorsal lymph space', 0.41935483870967744, 5.64885357140806, 1.5391147060347428, 'HP:0002715', 'Abnormality of the immune system'),
(466619, 'HP:0008290', 'Partial complement factor H deficiency', 'XPO:0100232', 'abnormal lymphatic system', 0.4482758620689655, 5.64885357140806, 1.5913028324062968, 'HP:0002715', 'Abnormality of the immune system'),
(466620, 'HP:0008290', 'Partial complement factor H deficiency', 'XPO:0100581', 'abnormal immune system', 0.4482758620689655, 5.64885357140806, 1.5913028324062968, 'HP:0002715', 'Abnormality of the immune system'),
(466621, 'HP:0008290', 'Partial complement factor H deficiency', 'XPO:0100599', 'abnormal adult immune system', 0.43333333333333335, 5.64885357140806, 1.5645563421015427, 'HP:0002715', 'Abnormality of the immune system'),
(466622, 'HP:0008290', 'Partial complement factor H deficiency', 'XPO:0101221', 'abnormal larval immune system', 0.43333333333333335, 5.64885357140806, 1.5645563421015427, 'HP:0002715', 'Abnormality of the immune system'),
(466623, 'HP:0012683', 'Pineal cyst', 'XPO:0101496', 'abnormal subcommissural organ', 0.42857142857142855, 7.431510076152836, 1.784638027662693, 'UPHENO:0004618', 'abnormal diencephalon'),
(466624, 'HP:0012683', 'Pineal cyst', 'XPO:0101184', 'abnormal suprachiasmatic nucleus', 0.4125, 7.431510076152836, 1.7508563351723192, 'UPHENO:0004618', 'abnormal diencephalon'),
(466625, 'HP:0012683', 'Pineal cyst', 'XPO:0102243', 'abnormal hypophysis morphology', 0.44565217391304346, 9.57542522308115, 2.0657466124401376, 'UPHENO:0086771', 'abnormal neuroendocrine gland morphology'),
(466626, 'HP:0012683', 'Pineal cyst', 'XPO:0100611', 'abnormal hypophysis', 0.4605263157894737, 7.431510076152836, 1.8499745825613434, 'UPHENO:0004618', 'abnormal diencephalon'),
(466627, 'HP:0012683', 'Pineal cyst', 'XPO:0100233', 'abnormal pars nervosa', 0.44871794871794873, 7.431510076152836, 1.8261029426754856, 'UPHENO:0004618', 'abnormal diencephalon'),
(466628, 'HP:0012683', 'Pineal cyst', 'XPO:0100914', 'abnormal pars intermedia', 0.44871794871794873, 7.431510076152836, 1.8261029426754856, 'UPHENO:0004618', 'abnormal diencephalon'),
(466629, 'HP:0012683', 'Pineal cyst', 'XPO:0140405', 'abnormally necrotic adenohypophysis', 0.41836734693877553, 9.57542522308115, 2.0015107410131714, 'UPHENO:0086771', 'abnormal neuroendocrine gland morphology'),
(466630, 'HP:0012683', 'Pineal cyst', 'XPO:0130794', 'increased size of the pars intermedia', 0.41414141414141414, 9.57542522308115, 1.991376444294798, 'UPHENO:0086771', 'abnormal neuroendocrine gland morphology'),
(466631, 'HP:0012683', 'Pineal cyst', 'XPO:0140782', 'abnormally necrotic melanotrope', 0.40594059405940597, 9.57542522308115, 1.971561260379444, 'UPHENO:0086771', 'abnormal neuroendocrine gland morphology'),
(466632, 'HP:0012683', 'Pineal cyst', 'XPO:0100194', 'abnormal preoptic area', 0.4230769230769231, 7.431510076152836, 1.7731611367368427, 'UPHENO:0004618', 'abnormal diencephalon'),
(466633, 'HP:0012683', 'Pineal cyst', 'XPO:0100656', 'abnormal ventral hypothalamic nucleus', 0.4177215189873418, 7.431510076152836, 1.7619028569646793, 'UPHENO:0004618', 'abnormal diencephalon'),
(466634, 'HP:0012683', 'Pineal cyst', 'XPO:0127924', 'abnormally localised pars nervosa', 0.4069767441860465, 7.431510076152836, 1.739095102396209, 'UPHENO:0004618', 'abnormal diencephalon'),
(466635, 'HP:0012683', 'Pineal cyst', 'XPO:0140253', 'abnormally necrotic hypophysis', 0.422680412371134, 9.57542522308115, 2.0118013525000173, 'UPHENO:0086771', 'abnormal neuroendocrine gland morphology'),
(466636, 'HP:0012683', 'Pineal cyst', 'XPO:0140394', 'abnormally necrotic pars nervosa', 0.41414141414141414, 9.57542522308115, 1.991376444294798, 'UPHENO:0086771', 'abnormal neuroendocrine gland morphology'),
(466637, 'HP:0012683', 'Pineal cyst', 'XPO:0102361', 'abnormal thalamus morphology', 0.4146341463414634, 8.230482561721782, 1.8473329724112575, 'UPHENO:0087516', 'abnormal diencephalon morphology'),
(466638, 'HP:0012683', 'Pineal cyst', 'XPO:0103158', 'abnormal infundibulum morphology', 0.45263157894736844, 11.872199840740173, 2.3181312645087466, 'UPHENO:0086772', 'abnormal secretory circumventricular organ morphology'),
(466639, 'HP:0012683', 'Pineal cyst', 'XPO:0101420', 'abnormal magnocellular preoptic nucleus', 0.4074074074074074, 7.431510076152836, 1.7400150152362053, 'UPHENO:0004618', 'abnormal diencephalon'),
(466640, 'HP:0012683', 'Pineal cyst', 'XPO:0127341', 'abnormally localised pars intermedia', 0.4117647058823529, 7.431510076152836, 1.7492951611345682, 'UPHENO:0004618', 'abnormal diencephalon'),
(466641, 'HP:0012683', 'Pineal cyst', 'XPO:0130436', 'increased size of the pars nervosa', 0.40594059405940597, 9.57542522308115, 1.971561260379444, 'UPHENO:0086771', 'abnormal neuroendocrine gland morphology'),
(466642, 'HP:0012683', 'Pineal cyst', 'XPO:0101117', 'abnormal tuberal region', 0.4230769230769231, 7.431510076152836, 1.7731611367368427, 'UPHENO:0004618', 'abnormal diencephalon'),
(466643, 'HP:0012683', 'Pineal cyst', 'XPO:0100951', 'abnormal adenohypophysis', 0.45454545454545453, 7.431510076152836, 1.837922502589273, 'UPHENO:0004618', 'abnormal diencephalon'),
(466644, 'HP:0012683', 'Pineal cyst', 'XPO:0126937', 'abnormally localised pineal gland', 0.43023255813953487, 12.082766826679832, 2.2799999300978, 'UPHENO:0002591', 'abnormal pineal body'),
(466645, 'HP:0012683', 'Pineal cyst', 'XPO:0126700', 'abnormally localised infundibulum', 0.4166666666666667, 7.431510076152836, 1.7596768259343385, 'UPHENO:0004618', 'abnormal diencephalon'),
(466646, 'HP:0012683', 'Pineal cyst', 'XPO:0100590', 'abnormal hypothalamus', 0.4342105263157895, 7.431510076152836, 1.7963406974979483, 'UPHENO:0004618', 'abnormal diencephalon'),
(466647, 'HP:0012683', 'Pineal cyst', 'XPO:0101284', 'abnormal ventromedial thalamic nucleus', 0.4177215189873418, 7.431510076152836, 1.7619028569646793, 'UPHENO:0004618', 'abnormal diencephalon'),
(466648, 'HP:0012683', 'Pineal cyst', 'XPO:0127365', 'abnormally localised melanotrope', 0.40229885057471265, 7.431510076152836, 1.7290714160122713, 'UPHENO:0004618', 'abnormal diencephalon'),
(466649, 'HP:0012683', 'Pineal cyst', 'XPO:0102123', 'abnormal pars distalis morphology', 0.43617021276595747, 9.57542522308115, 2.0436524305458157, 'UPHENO:0086771', 'abnormal neuroendocrine gland morphology'),
(466650, 'HP:0012683', 'Pineal cyst', 'XPO:0126843', 'abnormally localised pars distalis', 0.4069767441860465, 7.431510076152836, 1.739095102396209, 'UPHENO:0004618', 'abnormal diencephalon'),
(466651, 'HP:0012683', 'Pineal cyst', 'XPO:0100698', 'abnormal optic stalk', 0.4230769230769231, 7.431510076152836, 1.7731611367368427, 'UPHENO:0004618', 'abnormal diencephalon'),
(466652, 'HP:0012683', 'Pineal cyst', 'XPO:0128490', 'decreased size of the infundibulum', 0.4215686274509804, 11.872199840740173, 2.237173884990745, 'UPHENO:0086772', 'abnormal secretory circumventricular organ morphology'),
(466653, 'HP:0012683', 'Pineal cyst', 'XPO:0101354', 'abnormal eminentia thalami', 0.4342105263157895, 7.431510076152836, 1.7963406974979483, 'UPHENO:0004618', 'abnormal diencephalon'),
(466654, 'HP:0012683', 'Pineal cyst', 'XPO:0102395', 'abnormal pretectum morphology', 0.40963855421686746, 8.230482561721782, 1.8361707374563103, 'UPHENO:0087516', 'abnormal diencephalon morphology'),
(466655, 'HP:0012683', 'Pineal cyst', 'XPO:0130518', 'increased size of the pars distalis', 0.40594059405940597, 9.57542522308115, 1.971561260379444, 'UPHENO:0086771', 'abnormal neuroendocrine gland morphology'),
(466656, 'HP:0012683', 'Pineal cyst', 'XPO:0101293', 'abnormal posterior hypothalamus', 0.42857142857142855, 7.431510076152836, 1.784638027662693, 'UPHENO:0004618', 'abnormal diencephalon'),
(466657, 'HP:0012683', 'Pineal cyst', 'XPO:0102546', 'abnormal pars intermedia morphology', 0.44086021505376344, 9.57542522308115, 2.054610430976828, 'UPHENO:0086771', 'abnormal neuroendocrine gland morphology'),
(466658, 'HP:0012683', 'Pineal cyst', 'XPO:0101053', 'abnormal anterior hypothalamus', 0.42857142857142855, 7.431510076152836, 1.784638027662693, 'UPHENO:0004618', 'abnormal diencephalon'),
(466659, 'HP:0012683', 'Pineal cyst', 'XPO:0101068', 'abnormal pineal gland', 0.47435897435897434, 12.082766826679832, 2.394069522658539, 'UPHENO:0002591', 'abnormal pineal body'),
(466660, 'HP:0012683', 'Pineal cyst', 'XPO:0129318', 'decreased size of the pars intermedia', 0.41414141414141414, 9.57542522308115, 1.991376444294798, 'UPHENO:0086771', 'abnormal neuroendocrine gland morphology'),
(466661, 'HP:0012683', 'Pineal cyst', 'XPO:0101075', 'abnormal mammilary region', 0.4230769230769231, 7.431510076152836, 1.7731611367368427, 'UPHENO:0004618', 'abnormal diencephalon'),
(466662, 'HP:0012683', 'Pineal cyst', 'XPO:0102583', 'abnormal adenohypophysis morphology', 0.44086021505376344, 9.57542522308115, 2.054610430976828, 'UPHENO:0086771', 'abnormal neuroendocrine gland morphology'),
(466663, 'HP:0012683', 'Pineal cyst', 'XPO:0100783', 'abnormal supraoptoparaventricular region', 0.4125, 7.431510076152836, 1.7508563351723192, 'UPHENO:0004618', 'abnormal diencephalon'),
(466664, 'HP:0012683', 'Pineal cyst', 'XPO:0129041', 'decreased size of the pars distalis', 0.40594059405940597, 9.57542522308115, 1.971561260379444, 'UPHENO:0086771', 'abnormal neuroendocrine gland morphology'),
(466665, 'HP:0012683', 'Pineal cyst', 'XPO:0100575', 'abnormal diencephalon', 0.44, 7.431510076152836, 1.8082766473931051, 'UPHENO:0004618', 'abnormal diencephalon'),
(466666, 'HP:0012683', 'Pineal cyst', 'XPO:0100729', 'abnormal thalamus', 0.4342105263157895, 7.431510076152836, 1.7963406974979483, 'UPHENO:0004618', 'abnormal diencephalon'),
(466667, 'HP:0012683', 'Pineal cyst', 'XPO:0101564', 'abnormal anterior thalamic nucleus', 0.4177215189873418, 7.431510076152836, 1.7619028569646793, 'UPHENO:0004618', 'abnormal diencephalon'),
(466668, 'HP:0012683', 'Pineal cyst', 'XPO:0100491', 'abnormal pars distalis', 0.44871794871794873, 7.431510076152836, 1.8261029426754856, 'UPHENO:0004618', 'abnormal diencephalon'),
(466669, 'HP:0012683', 'Pineal cyst', 'XPO:0100157', 'abnormal optic tract', 0.4342105263157895, 7.431510076152836, 1.7963406974979483, 'UPHENO:0004618', 'abnormal diencephalon'),
(466670, 'HP:0012683', 'Pineal cyst', 'XPO:0129694', 'increased size of the adenohypophysis', 0.41, 9.57542522308115, 1.9813945446233747, 'UPHENO:0086771', 'abnormal neuroendocrine gland morphology'),
(466671, 'HP:0012683', 'Pineal cyst', 'XPO:0100998', 'abnormal rostral tuberal region', 0.4177215189873418, 7.431510076152836, 1.7619028569646793, 'UPHENO:0004618', 'abnormal diencephalon'),
(466672, 'HP:0012683', 'Pineal cyst', 'XPO:0128362', 'decreased size of the pineal gland', 0.5319148936170213, 13.167655724266345, 2.646520771458009, 'UPHENO:0020461', 'abnormal pineal body morphology'),
(466673, 'HP:0012683', 'Pineal cyst', 'XPO:0101595', 'abnormal prosomere 4', 0.4230769230769231, 7.431510076152836, 1.7731611367368427, 'UPHENO:0004618', 'abnormal diencephalon'),
(466674, 'HP:0012683', 'Pineal cyst', 'XPO:0101106', 'abnormal caudal tuberal region', 0.4177215189873418, 7.431510076152836, 1.7619028569646793, 'UPHENO:0004618', 'abnormal diencephalon'),
(466675, 'HP:0012683', 'Pineal cyst', 'XPO:0101123', 'abnormal third ventricle', 0.4230769230769231, 7.431510076152836, 1.7731611367368427, 'UPHENO:0004618', 'abnormal diencephalon'),
(466676, 'HP:0012683', 'Pineal cyst', 'XPO:0128214', 'decreased size of the adenohypophysis', 0.41, 9.57542522308115, 1.9813945446233747, 'UPHENO:0086771', 'abnormal neuroendocrine gland morphology'),
(466677, 'HP:0012683', 'Pineal cyst', 'XPO:0101351', 'abnormal dorsal habenular nucleus', 0.4074074074074074, 7.431510076152836, 1.7400150152362053, 'UPHENO:0004618', 'abnormal diencephalon'),
(466678, 'HP:0012683', 'Pineal cyst', 'XPO:0102207', 'abnormal diencephalon morphology', 0.41975308641975306, 8.230482561721782, 1.8587012826182354, 'UPHENO:0087516', 'abnormal diencephalon morphology'),
(466679, 'HP:0012683', 'Pineal cyst', 'XPO:0100263', 'abnormal prethalamus', 0.42857142857142855, 7.431510076152836, 1.784638027662693, 'UPHENO:0004618', 'abnormal diencephalon'),
(466680, 'HP:0012683', 'Pineal cyst', 'XPO:0127544', 'abnormally localised neurohypophysis', 0.4117647058823529, 7.431510076152836, 1.7492951611345682, 'UPHENO:0004618', 'abnormal diencephalon'),
(466681, 'HP:0012683', 'Pineal cyst', 'XPO:0101895', 'abnormal prethalamus morphology', 0.40963855421686746, 8.230482561721782, 1.8361707374563103, 'UPHENO:0087516', 'abnormal diencephalon morphology'),
(466682, 'HP:0012683', 'Pineal cyst', 'XPO:0101865', 'abnormal pars nervosa morphology', 0.43617021276595747, 9.57542522308115, 2.0436524305458157, 'UPHENO:0086771', 'abnormal neuroendocrine gland morphology'),
(466683, 'HP:0012683', 'Pineal cyst', 'XPO:0140316', 'abnormally necrotic pars distalis', 0.41414141414141414, 9.57542522308115, 1.991376444294798, 'UPHENO:0086771', 'abnormal neuroendocrine gland morphology'),
(466684, 'HP:0012683', 'Pineal cyst', 'XPO:0129842', 'increased size of the pineal gland', 0.5263157894736842, 13.167655724266345, 2.632554865151896, 'UPHENO:0020461', 'abnormal pineal body morphology'),
(466685, 'HP:0012683', 'Pineal cyst', 'XPO:0128957', 'decreased size of the neurohypophysis', 0.41, 9.57542522308115, 1.9813945446233747, 'UPHENO:0086771', 'abnormal neuroendocrine gland morphology'),
(466686, 'HP:0012683', 'Pineal cyst', 'XPO:0100763', 'abnormal pretectum', 0.4342105263157895, 7.431510076152836, 1.7963406974979483, 'UPHENO:0004618', 'abnormal diencephalon'),
(466687, 'HP:0012683', 'Pineal cyst', 'XPO:0140721', 'abnormally necrotic pineal gland', 0.5434782608695652, 13.167655724266345, 2.67513263834776, 'UPHENO:0020461', 'abnormal pineal body morphology'),
(466688, 'HP:0012683', 'Pineal cyst', 'XPO:0141184', 'abnormally necrotic pars intermedia', 0.422680412371134, 9.57542522308115, 2.0118013525000173, 'UPHENO:0086771', 'abnormal neuroendocrine gland morphology'),
(466689, 'HP:0012683', 'Pineal cyst', 'XPO:0129970', 'increased size of the infundibulum', 0.4215686274509804, 11.872199840740173, 2.237173884990745, 'UPHENO:0086772', 'abnormal secretory circumventricular organ morphology'),
(466690, 'HP:0012683', 'Pineal cyst', 'XPO:0100695', 'abnormal zona limitans intrathalamica', 0.42857142857142855, 7.431510076152836, 1.784638027662693, 'UPHENO:0004618', 'abnormal diencephalon'),
(466691, 'HP:0012683', 'Pineal cyst', 'XPO:0101947', 'abnormal neurohypophysis morphology', 0.44086021505376344, 9.57542522308115, 2.054610430976828, 'UPHENO:0086771', 'abnormal neuroendocrine gland morphology'),
(466692, 'HP:0012683', 'Pineal cyst', 'XPO:0101186', 'abnormal optic chiasm', 0.4342105263157895, 7.431510076152836, 1.7963406974979483, 'UPHENO:0004618', 'abnormal diencephalon'),
(466693, 'HP:0012683', 'Pineal cyst', 'XPO:0100946', 'abnormal melanotrope', 0.4375, 7.431510076152836, 1.8031321799349227, 'UPHENO:0004618', 'abnormal diencephalon'),
(466694, 'HP:0012683', 'Pineal cyst', 'XPO:0100971', 'abnormal prethalamus basal plate', 0.4177215189873418, 7.431510076152836, 1.7619028569646793, 'UPHENO:0004618', 'abnormal diencephalon'),
(466695, 'HP:0012683', 'Pineal cyst', 'XPO:0100315', 'abnormal neurohypophysis', 0.45454545454545453, 7.431510076152836, 1.837922502589273, 'UPHENO:0004618', 'abnormal diencephalon'),
(466696, 'HP:0012683', 'Pineal cyst', 'XPO:0101268', 'abnormal lateral hypothalamic nucleus', 0.4177215189873418, 7.431510076152836, 1.7619028569646793, 'UPHENO:0004618', 'abnormal diencephalon'),
(466697, 'HP:0012683', 'Pineal cyst', 'XPO:0127050', 'abnormally localised adenohypophysis', 0.4117647058823529, 7.431510076152836, 1.7492951611345682, 'UPHENO:0004618', 'abnormal diencephalon'),
(466698, 'HP:0012683', 'Pineal cyst', 'XPO:0101588', 'abnormal central nucleus of the thalamus', 0.4177215189873418, 7.431510076152836, 1.7619028569646793, 'UPHENO:0004618', 'abnormal diencephalon'),
(466699, 'HP:0012683', 'Pineal cyst', 'XPO:0102620', 'abnormal habenula morphology', 0.40476190476190477, 8.230482561721782, 1.8252084261234798, 'UPHENO:0087516', 'abnormal diencephalon morphology'),
(466700, 'HP:0012683', 'Pineal cyst', 'XPO:0100962', 'abnormal dorsal thalamus', 0.42857142857142855, 7.431510076152836, 1.784638027662693, 'UPHENO:0004618', 'abnormal diencephalon'),
(466701, 'HP:0012683', 'Pineal cyst', 'XPO:0101140', 'abnormal ventrolateral thalamic nucleus', 0.4177215189873418, 7.431510076152836, 1.7619028569646793, 'UPHENO:0004618', 'abnormal diencephalon'),
(466702, 'HP:0012683', 'Pineal cyst', 'XPO:0140341', 'abnormally necrotic neurohypophysis', 0.41836734693877553, 9.57542522308115, 2.0015107410131714, 'UPHENO:0086771', 'abnormal neuroendocrine gland morphology'),
(466703, 'HP:0012683', 'Pineal cyst', 'XPO:0102578', 'abnormal melanotrope morphology', 0.422680412371134, 9.57542522308115, 2.0118013525000173, 'UPHENO:0086771', 'abnormal neuroendocrine gland morphology'),
(466704, 'HP:0012683', 'Pineal cyst', 'XPO:0100988', 'abnormal habenula', 0.4230769230769231, 7.431510076152836, 1.7731611367368427, 'UPHENO:0004618', 'abnormal diencephalon'),
(466705, 'HP:0012683', 'Pineal cyst', 'XPO:0102755', 'abnormal third ventricle morphology', 0.40963855421686746, 8.230482561721782, 1.8361707374563103, 'UPHENO:0087516', 'abnormal diencephalon morphology'),
(466706, 'HP:0012683', 'Pineal cyst', 'XPO:0102700', 'abnormal pineal gland morphology', 0.5747126436781609, 13.167655724266345, 2.750930430297535, 'UPHENO:0020461', 'abnormal pineal body morphology'),
(466707, 'HP:0012683', 'Pineal cyst', 'XPO:0102986', 'abnormal eminentia thalami morphology', 0.4146341463414634, 8.230482561721782, 1.8473329724112575, 'UPHENO:0087516', 'abnormal diencephalon morphology'),
(466708, 'HP:0012683', 'Pineal cyst', 'XPO:0103128', 'abnormal subcommissural organ morphology', 0.40476190476190477, 8.230482561721782, 1.8252084261234798, 'UPHENO:0087516', 'abnormal diencephalon morphology'),
(466709, 'HP:0012683', 'Pineal cyst', 'XPO:0102327', 'abnormal zona limitans intrathalamica morphology', 0.42168674698795183, 10.61213700143767, 2.1154189964937746, 'UPHENO:0087517', 'abnormal dorsal plus ventral thalamus morphology'),
(466710, 'HP:0012683', 'Pineal cyst', 'XPO:0100195', 'abnormal retromammillary area', 0.42857142857142855, 7.431510076152836, 1.784638027662693, 'UPHENO:0004618', 'abnormal diencephalon'),
(466711, 'HP:0012683', 'Pineal cyst', 'XPO:0130435', 'increased size of the neurohypophysis', 0.41, 9.57542522308115, 1.9813945446233747, 'UPHENO:0086771', 'abnormal neuroendocrine gland morphology'),
(466712, 'HP:0012683', 'Pineal cyst', 'XPO:0100473', 'abnormal ventral habenular nucleus', 0.4074074074074074, 7.431510076152836, 1.7400150152362053, 'UPHENO:0004618', 'abnormal diencephalon'),
(466713, 'HP:0012683', 'Pineal cyst', 'XPO:0100909', 'abnormal choroid fissure', 0.4024390243902439, 7.431510076152836, 1.7293726217311336, 'UPHENO:0004618', 'abnormal diencephalon'),
(466714, 'HP:0012683', 'Pineal cyst', 'XPO:0128958', 'decreased size of the pars nervosa', 0.40594059405940597, 9.57542522308115, 1.971561260379444, 'UPHENO:0086771', 'abnormal neuroendocrine gland morphology'),
(466715, 'HP:0012683', 'Pineal cyst', 'XPO:0101526', 'abnormal infundibulum', 0.4605263157894737, 7.431510076152836, 1.8499745825613434, 'UPHENO:0004618', 'abnormal diencephalon'),
(466716, 'HP:0012683', 'Pineal cyst', 'XPO:0140252', 'abnormally necrotic infundibulum', 0.43, 11.872199840740173, 2.2594348699438704, 'UPHENO:0086772', 'abnormal secretory circumventricular organ morphology'),
(466717, 'HP:0012683', 'Pineal cyst', 'XPO:0102594', 'abnormal dorsal thalamus morphology', 0.40963855421686746, 8.230482561721782, 1.8361707374563103, 'UPHENO:0087516', 'abnormal diencephalon morphology'),
(466718, 'HP:0001829', 'Foot polydactyly', 'XPO:0115785', 'duplicated hindlimb digit 5 in regenerating hindlimb', 0.5698924731182796, 13.257853533237922, 2.7487362438576897, 'HP:0001829', 'Foot polydactyly'),
(466719, 'HP:0001829', 'Foot polydactyly', 'XPO:0102051', 'abnormal hindlimb digit 2 morphology', 0.4175824175824176, 7.639349617137506, 1.7860733696804272, 'HP:0001780', 'Abnormal toe morphology'),
(466720, 'HP:0001829', 'Foot polydactyly', 'XPO:0101872', 'abnormal hindlimb digit 1 morphology', 0.4175824175824176, 7.639349617137506, 1.7860733696804272, 'UPHENO:0088132', 'abnormal pedal digit morphology'),
(466721, 'HP:0001829', 'Foot polydactyly', 'XPO:0101809', 'abnormal hindlimb digit morphology', 0.42696629213483145, 7.639349617137506, 1.806030116125101, 'HP:0001780', 'Abnormal toe morphology'),
(466722, 'HP:0001829', 'Foot polydactyly', 'XPO:0139979', 'abnormally necrotic claw primordium', 0.40860215053763443, 7.639349617137506, 1.7667639011116452, 'HP:0001780', 'Abnormal toe morphology'),
(466723, 'HP:0001829', 'Foot polydactyly', 'XPO:0102180', 'abnormal hindlimb digit 3 morphology', 0.4175824175824176, 7.639349617137506, 1.7860733696804272, 'HP:0001780', 'Abnormal toe morphology'),
(466724, 'HP:0001829', 'Foot polydactyly', 'XPO:0103632', 'abnormally increased number of digit', 0.5909090909090909, 11.404694921567193, 2.5959849591626676, 'UPHENO:0056085', 'abnormally increased number of digit in the limb'),
(466725, 'HP:0001829', 'Foot polydactyly', 'XPO:0103627', 'abnormally increased number of hindlimb digit', 0.654320987654321, 13.257853533237922, 2.9453169299830138, 'HP:0001829', 'Foot polydactyly'),
(466726, 'HP:0001829', 'Foot polydactyly', 'XPO:0102876', 'abnormal hindlimb digit 4 morphology', 0.4175824175824176, 7.639349617137506, 1.7860733696804272, 'HP:0001780', 'Abnormal toe morphology'),
(466727, 'HP:0001829', 'Foot polydactyly', 'XPO:0115782', 'duplicated hindlimb digit 2 in regenerating hindlimb', 0.5698924731182796, 13.257853533237922, 2.7487362438576897, 'HP:0001829', 'Foot polydactyly'),
(466728, 'HP:0001829', 'Foot polydactyly', 'XPO:0100178', 'abnormal digit', 0.4307692307692308, 6.393467666143939, 1.659550887587595, 'HP:0011297', 'Abnormal digit morphology'),
(466729, 'HP:0001829', 'Foot polydactyly', 'XPO:0101810', 'abnormal digit morphology', 0.4189189189189189, 6.466375519622663, 1.6458696916840314, 'UPHENO:0086700', 'abnormal digit morphology'),
(466730, 'HP:0001829', 'Foot polydactyly', 'XPO:0102880', 'abnormal digit-joint region morphology', 0.4189189189189189, 6.466375519622663, 1.6458696916840314, 'UPHENO:0086700', 'abnormal digit morphology'),
(466731, 'HP:0001829', 'Foot polydactyly', 'XPO:0115783', 'duplicated hindlimb digit 3 in regenerating hindlimb', 0.5698924731182796, 13.257853533237922, 2.7487362438576897, 'HP:0001829', 'Foot polydactyly'),
(466732, 'HP:0001829', 'Foot polydactyly', 'XPO:0124986', 'absent digit', 0.40789473684210525, 6.393467666143939, 1.6148875537294511, 'HP:0011297', 'Abnormal digit morphology'),
(466733, 'HP:0001829', 'Foot polydactyly', 'XPO:0115781', 'duplicated hindlimb digit 1 in regenerating hindlimb', 0.5698924731182796, 13.257853533237922, 2.7487362438576897, 'HP:0001829', 'Foot polydactyly'),
(466734, 'HP:0001829', 'Foot polydactyly', 'XPO:0102566', 'abnormal claw primordium morphology', 0.4318181818181818, 7.639349617137506, 1.8162626632581922, 'HP:0001780', 'Abnormal toe morphology'),
(466735, 'HP:0001829', 'Foot polydactyly', 'XPO:0101248', 'abnormal digit-joint region', 0.4117647058823529, 6.393467666143939, 1.622530225640833, 'UPHENO:0002905', 'abnormal digit'),
(466736, 'HP:0001829', 'Foot polydactyly', 'XPO:0125443', 'absent digit-joint region', 0.41333333333333333, 6.393467666143939, 1.625617821631567, 'HP:0011297', 'Abnormal digit morphology'),
(466737, 'HP:0001829', 'Foot polydactyly', 'XPO:0103289', 'absent hindlimb digit', 0.4077669902912621, 7.639349617137506, 1.7649573935828782, 'UPHENO:0088132', 'abnormal pedal digit morphology'),
(466738, 'HP:0001829', 'Foot polydactyly', 'XPO:0103413', 'abnormally increased number of hindlimb digit in the regenerating hindlimb', 0.6091954022988506, 13.257853533237922, 2.841940079734285, 'HP:0001829', 'Foot polydactyly'),
(466739, 'HP:0001829', 'Foot polydactyly', 'XPO:0115784', 'duplicated hindlimb digit 4 in regenerating hindlimb', 0.5698924731182796, 13.257853533237922, 2.7487362438576897, 'HP:0001829', 'Foot polydactyly'),
(466740, 'HP:0001829', 'Foot polydactyly', 'XPO:0102948', 'abnormal hindlimb digit 5 morphology', 0.4175824175824176, 7.639349617137506, 1.7860733696804272, 'UPHENO:0088132', 'abnormal pedal digit morphology'),
(466741, 'HP:0001829', 'Foot polydactyly', 'XPO:0115779', 'duplicated hindlimb digit in regenerating hindlimb', 0.5888888888888889, 13.257853533237922, 2.7941729789403, 'HP:0001829', 'Foot polydactyly'),
(466742, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0101448', 'abnormal myelin accumulating cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(466743, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0101240', 'abnormal ciliated non-epidermal cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(466744, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0100688', 'abnormal adipose tissue', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(466745, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0101472', 'abnormal zygote cortex', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(466746, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0100205', 'abnormal limb segment', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(466747, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0101132', 'abnormal apoptotic cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(466748, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0100108', 'abnormal cell part', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(466749, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0141770', 'abnormal urate homeostasis', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(466750, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0107339', 'abnormal yolk platelet', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(466751, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0141315', 'abnormal anatomical region', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(466752, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0101061', 'abnormal plasma membrane', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(466753, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0141738', 'abnormal carbon dioxide homeostasis', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(466754, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0141276', 'decreased surface breathing', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(466755, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0100386', 'abnormal limb', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(466756, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0101109', 'abnormal egg cell-free extract', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(466757, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0141266', 'abnormal surface breathing', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(466758, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0141959', 'absent cilium motility in floor plate', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(466759, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0141775', 'abnormal nitrogen compound metabolic process', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(466760, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0141796', 'abnormal demethylation', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(466761, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0141904', 'abnormal glucosamine metabolic process', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(466762, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0141784', 'abnormal cellular hormone metabolic process', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(466763, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0141777', 'abnormal catabolic process', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(466764, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0100423', 'abnormal process', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(466765, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0101498', 'abnormal stage II oocyte', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(466766, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0100643', 'abnormal thoracic region', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(466767, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0100477', 'abnormal pericyte', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(466768, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0100902', 'abnormal spermatocyte', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(466769, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0100515', 'abnormal somatic stem cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(466770, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0100465', 'abnormal skeletal system', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(466771, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0141600', 'absent metamorphosis', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(466772, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0100887', 'abnormal right-dorsal blastomere', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(466773, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0100014', 'abnormal tissue', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(466774, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0141263', 'abnormal visually guided collision avoidance behavior', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(466775, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0100653', 'abnormal myoblast', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(466776, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0100337', 'abnormal zygote', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(466777, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0100842', 'abnormal left-dorsal blastomere', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(466778, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0100218', 'abnormal epithelial cell', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(466779, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0100025', 'abnormal oocyte', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(466780, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0100104', 'abnormal embryonic structure', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(466781, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0131685', 'abnormal cortical actin cytoskeleton', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(466782, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0100070', 'abnormal anatomical system', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(466783, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0107276', 'abnormal dorsal region', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(466784, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0141797', 'abnormal hydrogen metabolic process', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(466785, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0116433', 'abnormal axis specification', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(466786, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0141783', 'abnormal collagen metabolic process', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(466787, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0101141', 'abnormal Keller explant', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(466788, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0141772', 'abnormal water homeostasis', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(466789, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0100691', 'abnormal keratin accumulating cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(466790, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0100429', 'abnormal spermatid', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(466791, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0100728', 'abnormal cell condensation', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(466792, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0100574', 'abnormal gastrula cell', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(466793, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0100917', 'abnormal stage III oocyte', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(466794, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0101378', 'abnormal blastomere D1', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(466795, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0101311', 'abnormal bottle cell', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(466796, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0133388', 'absent insulin receptor signaling pathway', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(466797, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0115509', 'abnormally semi-viable whole organism', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(466798, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0141960', 'absent cilium motility in brain', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(466799, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0131469', 'abnormal heart process', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(466800, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0101461', 'abnormal sperm entry point', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(466801, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0107260', 'abnormal anterior-posterior axis', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(466802, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0141958', 'absent cilium motility in left-right organizer', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(466803, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:00000000', 'Xenopus phenotype', 0.5714285714285714, 1.4755025719078136, 0.918228907628411, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(466804, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0107271', 'abnormal apical region', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(466805, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0100295', 'abnormal extracellular matrix', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(466806, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0101435', 'abnormal paracrine cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(466807, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0100486', 'abnormal oral evagination', 0.4230769230769231, 4.96264005835567, 1.4489922312515684, 'HP:0002664', 'Neoplasm'),
(466808, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0100852', 'abnormal interdigital region', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(466809, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0100665', 'abnormal egg jelly', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(466810, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0100523', 'abnormal midgut', 0.4230769230769231, 4.96264005835567, 1.4489922312515684, 'HP:0002664', 'Neoplasm'),
(466811, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0101575', 'abnormal vitelline membrane', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(466812, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0100010', 'abnormal multicellular anatomical structure', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(466813, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0107258', 'abnormal anatomical axis', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(466814, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0101547', 'abnormal lampbrush chromosome', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(466815, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0107263', 'abnormal anatomical side', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(466816, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0142057', 'abnormal desmosome', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(466817, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0107312', 'abnormal filopodium', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(466818, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0100888', 'abnormal microtubule', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(466819, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0100986', 'abnormal gut epithelium', 0.4074074074074074, 4.96264005835567, 1.421905875953408, 'HP:0002664', 'Neoplasm'),
(466820, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0100501', 'abnormal urogenital system', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(466821, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0141776', 'abnormal metabolic process', 0.5263157894736842, 1.8210412618256888, 0.9790009036675816, 'HP:0000118', 'Phenotypic abnormality'),
(466822, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0100172', 'abnormal stem cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(466823, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0115391', 'abnormally undifferentiated alimentary system', 0.4583333333333333, 4.96264005835567, 1.508158930643479, 'HP:0002664', 'Neoplasm'),
(466824, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0141898', 'abnormal maltose metabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(466825, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0101463', 'abnormal right-ventral blastomere', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(466826, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0100225', 'abnormal endocrine system', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(466827, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0131694', 'abnormal RNA polymerase II activity', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(466828, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0101409', 'abnormal perivitelline space', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(466829, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0141791', 'abnormal primary metabolic process', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(466830, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0131719', 'abnormal activation of meiosis', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(466831, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0100377', 'abnormal connective tissue', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(466832, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0100724', 'abnormal kinetochore', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(466833, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0100317', 'abnormal respiratory system', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(466834, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0141962', 'absent cilium motility in pronephric kidney', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(466835, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0101513', 'abnormal basal body', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(466836, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0100503', 'abnormal blastomere D2', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(466837, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0100239', 'abnormal acellular anatomical structure', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(466838, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0107259', 'abnormal animal-vegetal axis', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(466839, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0100735', 'abnormal hindgut', 0.4230769230769231, 4.96264005835567, 1.4489922312515684, 'HP:0002664', 'Neoplasm'),
(466840, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0131725', 'abnormal phosphorylation of RNA polymerase II C-terminal domain', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(466841, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0101264', 'abnormal mitotic spindle', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(466842, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0100156', 'abnormal foregut', 0.4230769230769231, 4.96264005835567, 1.4489922312515684, 'HP:0002664', 'Neoplasm'),
(466843, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0100392', 'abnormal cilium', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(466844, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0101366', 'abnormal morula cell', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(466845, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0131687', 'abnormal astral microtubule', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(466846, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0100545', 'abnormal male organism', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(466847, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0100344', 'abnormal portion of organism substance', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(466848, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0101389', 'abnormal wedge region', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(466849, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0100791', 'abnormal multiciliated cell precursor', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(466850, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0133340', 'abnormal cell adhesion', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(466851, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0131691', 'abnormal molecular function', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(466852, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0115512', 'abnormally semi-erect whole organism', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(466853, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0100762', 'abnormal intersomitic region', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(466854, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0116429', 'abnormal behavior', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(466855, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0101241', 'abnormal nucleate erythrocyte', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(466856, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0100232', 'abnormal lymphatic system', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(466857, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0131703', 'abnormal cell division', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(466858, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0100802', 'abnormal exocrine cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(466859, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0100976', 'abnormal multiciliated cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(466860, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0133403', 'abnormal developmental process', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(466861, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0100715', 'abnormal ciliated cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(466862, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0107278', 'abnormal medial region', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(466863, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0101535', 'abnormal absorptive cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(466864, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0141499', 'abnormal tadpole', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(466865, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0133401', 'absent determination of left/right symmetry in lateral plate mesoderm', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(466866, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0100277', 'abnormal blastocoel', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(466867, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0100308', 'abnormal early embryonic cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(466868, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0141794', 'abnormal prosthetic group metabolic process', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(466869, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0131722', 'abnormal determination of left/right symmetry', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(466870, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0101072', 'abnormal mitochondrial cloud', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(466871, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0141265', 'abnormal escape behavior', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(466872, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0101497', 'abnormal ciliary axoneme', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(466873, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0116434', 'abnormal biological process', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(466874, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0100003', 'abnormal organism subdivision', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(466875, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0141787', 'abnormal hormone metabolic process', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(466876, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0101381', 'abnormal ventral foregut', 0.4074074074074074, 4.96264005835567, 1.421905875953408, 'HP:0002664', 'Neoplasm'),
(466877, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0101570', 'abnormal forelimb region', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(466878, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0101373', 'abnormal oxygen accumulating cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(466879, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0101347', 'abnormal hindlimb region', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(466880, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0100372', 'abnormal hematological system', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(466881, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0100289', 'abnormal chondroblast', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(466882, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0107284', 'abnormal migrating myoblast', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(466883, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0101333', 'abnormal barrier epithelial cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(466884, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0100581', 'abnormal immune system', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(466885, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0100899', 'abnormal secondary spermatogonium', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(466886, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0141975', 'abnormal cilium motility', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(466887, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0100862', 'abnormal blastomere V1', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(466888, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0141877', 'abnormal 2-deoxyribose 1-phosphate metabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(466889, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0141892', 'abnormal inositol metabolic process', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(466890, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0141272', 'absent surface breathing', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(466891, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0115505', 'dead whole organism', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(466892, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0131729', 'abnormal regulation of growth rate', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(466893, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0141798', 'abnormal lipid metabolic process', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(466894, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0141745', 'abnormal creatinine homeostasis', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(466895, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0141754', 'abnormal homeostatic process', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(466896, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0101071', 'abnormal endoplasmic reticulum', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(466897, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0100006', 'abnormal anatomical structure', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(466898, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0100823', 'abnormal blood', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(466899, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0100084', 'abnormal anatomical group', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(466900, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0141267', 'abnormal resting posture', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(466901, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0131666', 'abnormal adherens junction', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(466902, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0100028', 'abnormal anatomical cluster', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(466903, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0100152', 'abnormal alimentary system', 0.4782608695652174, 4.96264005835567, 1.5405961669588706, 'HP:0002664', 'Neoplasm'),
(466904, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0100969', 'abnormal disaggregated/reaggregated ectoderm treated with activin', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(466905, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0100784', 'abnormal left blastomere', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(466906, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0100202', 'abnormal embryo', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(466907, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0100907', 'abnormal cytoplasm', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(466908, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0101101', 'abnormal posterior foregut', 0.4074074074074074, 4.96264005835567, 1.421905875953408, 'HP:0002664', 'Neoplasm'),
(466909, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0141781', 'abnormal secondary metabolic process', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(466910, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0100009', 'abnormal multi-tissue structure', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(466911, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0100551', 'abnormal oocyte cortex', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(466912, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0100032', 'abnormal nervous system', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(466913, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0101157', 'abnormal female organism', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(466914, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0101467', 'abnormal alkali secreting cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(466915, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0101451', 'abnormal dorsal lymph space', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(466916, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0141809', 'abnormal catalytic activity', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(466917, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0101468', 'abnormal stage I oocyte', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(466918, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0101326', 'abnormal cementoblast', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(466919, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0100062', 'abnormal anatomical space', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(466920, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0141795', 'abnormal glycosylation', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(466921, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0100547', 'abnormal blastomere V2', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(466922, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0100481', 'abnormal anatomical line', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(466923, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0131730', 'abnormal regulation of protein folding', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(466924, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0101297', 'abnormal barrier cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(466925, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0101228', 'abnormal mesenchymal stem cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(466926, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0101200', 'abnormal joint region', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(466927, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0100638', 'abnormal polar body', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(466928, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0100533', 'abnormal melanoblast', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(466929, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0141964', 'absent cilium motility in olfactory pit', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(466930, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0100642', 'abnormal gustatory system', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(466931, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0100956', 'abnormal centrosome', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(466932, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0101113', 'abnormal stage IV oocyte', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(466933, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0141782', 'abnormal methylation', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(466934, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0107272', 'abnormal axial region', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(466935, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0101136', 'abnormal ooplasm', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(466936, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0131744', 'abnormal apical constriction', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(466937, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0101021', 'abnormal dorsal foregut', 0.4074074074074074, 4.96264005835567, 1.421905875953408, 'HP:0002664', 'Neoplasm'),
(466938, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0141778', 'abnormal biosynthetic process', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(466939, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0100258', 'abnormal organ part', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(466940, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0100585', 'abnormal elastica externa', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(466941, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0100721', 'abnormal centromere', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(466942, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0141792', 'abnormal small molecule metabolic process', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(466943, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0100890', 'abnormal pharyngeal cavity', 0.44, 4.96264005835567, 1.4776879324392194, 'HP:0002664', 'Neoplasm'),
(466944, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0100493', 'abnormal liver and biliary system', 0.4583333333333333, 4.96264005835567, 1.508158930643479, 'HP:0002664', 'Neoplasm'),
(466945, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0101569', 'abnormal activin-induced ectoderm', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(466946, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0142054', 'abnormal digestive tract', 0.44, 4.96264005835567, 1.4776879324392194, 'HP:0002664', 'Neoplasm'),
(466947, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0141743', 'abnormal chemical homeostasis within a tissue', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(466948, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0100437', 'abnormal proepicardium', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(466949, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0116494', 'absent biological process', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(466950, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0100176', 'abnormal stage VI oocyte', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(466951, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0100031', 'abnormal central nervous system', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(466952, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0100587', 'abnormal vestibuloauditory system', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(466953, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0100573', 'abnormal extraembryonic structure', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(466954, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0100004', 'abnormal cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(466955, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0101377', 'abnormal manicotto glandulare', 0.4230769230769231, 4.96264005835567, 1.4489922312515684, 'HP:0002664', 'Neoplasm'),
(466956, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0100546', 'abnormal whole organism', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(466957, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0141264', 'abnormal schooling behavior', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(466958, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0100417', 'abnormal dense regular connective tissue', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(466959, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0141907', 'abnormal putrescine metabolic process', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(466960, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0101004', 'abnormal acid secreting cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(466961, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0101411', 'abnormal marginal zone (sensu neural)', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(466962, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0141786', 'abnormal pigment metabolic process', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(466963, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0100704', 'abnormal Merkel cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(466964, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0100081', 'abnormal anatomical entity in vitro', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(466965, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0131723', 'abnormal pathway-restricted SMAD protein phosphorylation', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(466966, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0100894', 'abnormal nucleus', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(466967, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0107270', 'abnormal proximal-distal axis', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(466968, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0100549', 'abnormal mitotic cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(466969, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0141271', 'increased surface breathing', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(466970, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0100273', 'abnormal visual system', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(466971, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0115508', 'abnormally peramorphic growth of whole organism', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(466972, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0101480', 'abnormal stage V oocyte', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(466973, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0100674', 'abnormal secondary oogonium', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(466974, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0107273', 'abnormal basal region', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(466975, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0141911', 'abnormal ribose phosphate metabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(466976, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0101283', 'abnormal left-ventral blastomere', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(466977, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0141790', 'abnormal cellular metabolic process', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(466978, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0100626', 'abnormal primordial germ cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(466979, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0100599', 'abnormal adult immune system', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(466980, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0101220', 'abnormal centriole', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(466981, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0107288', 'abnormal larval alimentary system', 0.4583333333333333, 4.96264005835567, 1.508158930643479, 'HP:0002664', 'Neoplasm'),
(466982, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0141771', 'abnormal urea homeostasis', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(466983, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0141724', 'abnormal prevention of polyspermy', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(466984, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0101405', 'abnormal ring structure', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(466985, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0131667', 'abnormal actin cytoskeleton', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(466986, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0141860', 'abnormal malate-aspartate shuttle', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(466987, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0100274', 'abnormal sensory system', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(466988, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0128000', 'absent behavior', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(466989, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0107262', 'abnormal left-right axis', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(466990, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0100462', 'abnormal anterior foregut', 0.4074074074074074, 4.96264005835567, 1.421905875953408, 'HP:0002664', 'Neoplasm'),
(466991, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0100285', 'abnormal progenitor cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(466992, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0101237', 'abnormal mucus secreting cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(466993, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0101110', 'abnormal cell-free extract', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(466994, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0131677', 'abnormal actin filament', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(466995, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0101302', 'abnormal subcortical cytoplasm', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(466996, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0131669', 'abnormal Roux spot', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(466997, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0107261', 'abnormal dorsal-ventral axis', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(466998, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0100307', 'abnormal blastomere', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(466999, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0100026', 'abnormal germ cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(467000, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0131675', 'abnormal spindle microtubule', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(467001, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0131740', 'abnormal detection of nodal flow', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(467002, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0100989', 'abnormal right blastomere', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(467003, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0141748', 'abnormal gas homeostasis', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(467004, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0100754', 'abnormal electrically active cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(467005, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0107253', 'abnormal enteric nervous system', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(467006, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0100422', 'abnormal notochord', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(467007, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0101221', 'abnormal larval immune system', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(467008, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0100427', 'abnormal olfactory system', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(467009, 'HP:0012316', 'Fibrous tissue neoplasm', 'XPO:0131745', 'abnormal axis elongation', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(467010, 'HP:0034590', 'Abnormal circulating thyroxine-binding globulin concentration', 'XPO:0141873', 'abnormal tricarboxylic acid metabolic process', 0.4339622641509434, 7.41682187759612, 1.7940515084037758, 'HP:0430071', 'Abnormal circulating organic compound concentration'),
(467011, 'HP:0034590', 'Abnormal circulating thyroxine-binding globulin concentration', 'XPO:0141869', 'abnormal alpha-amino acid metabolic process', 0.40350877192982454, 7.41682187759612, 1.729957423594889, 'HP:0430071', 'Abnormal circulating organic compound concentration'),
(467012, 'HP:0007592', 'Aplasia/Hypoplastia of the eccrine sweat glands', 'XPO:0102954', 'abnormal iridophore morphology', 0.40384615384615385, 7.420886955069779, 1.7311547172139254, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(467013, 'HP:0007592', 'Aplasia/Hypoplastia of the eccrine sweat glands', 'XPO:0102886', 'abnormal stratum compactum morphology', 0.42, 7.420886955069779, 1.7654383368244009, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(467014, 'HP:0007592', 'Aplasia/Hypoplastia of the eccrine sweat glands', 'XPO:0102910', 'abnormal pigment cell morphology', 0.42, 7.420886955069779, 1.7654383368244009, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(467015, 'HP:0007592', 'Aplasia/Hypoplastia of the eccrine sweat glands', 'XPO:0102626', 'abnormal granular gland morphology', 0.42857142857142855, 7.420886955069779, 1.7833620281931915, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(467016, 'HP:0007592', 'Aplasia/Hypoplastia of the eccrine sweat glands', 'XPO:0103019', 'abnormal melanophore morphology', 0.40384615384615385, 7.420886955069779, 1.7311547172139254, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(467017, 'HP:0007592', 'Aplasia/Hypoplastia of the eccrine sweat glands', 'XPO:0103223', 'abnormal xanthophore morphology', 0.40384615384615385, 7.420886955069779, 1.7311547172139254, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(467018, 'HP:0007592', 'Aplasia/Hypoplastia of the eccrine sweat glands', 'XPO:0102176', 'abnormal neuromast support cell morphology', 0.42, 7.420886955069779, 1.7654383368244009, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(467019, 'HP:0007592', 'Aplasia/Hypoplastia of the eccrine sweat glands', 'XPO:0102561', 'abnormal dermis morphology', 0.4375, 7.420886955069779, 1.8018429573198183, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(467020, 'HP:0007592', 'Aplasia/Hypoplastia of the eccrine sweat glands', 'XPO:0102945', 'abnormal Eberth-Kastschenko layer morphology', 0.42, 7.420886955069779, 1.7654383368244009, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(467021, 'HP:0007592', 'Aplasia/Hypoplastia of the eccrine sweat glands', 'XPO:0103147', 'abnormal neuromast mantle cell morphology', 0.42, 7.420886955069779, 1.7654383368244009, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(467022, 'HP:0007592', 'Aplasia/Hypoplastia of the eccrine sweat glands', 'XPO:0102615', 'abnormal skin gland morphology', 0.44680851063829785, 7.420886955069779, 1.8209106095604752, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(467023, 'HP:0007592', 'Aplasia/Hypoplastia of the eccrine sweat glands', 'XPO:0102727', 'abnormal skin seromucous gland morphology', 0.42857142857142855, 7.420886955069779, 1.7833620281931915, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(467024, 'HP:0007592', 'Aplasia/Hypoplastia of the eccrine sweat glands', 'XPO:0102139', 'abnormal skin morphology', 0.44680851063829785, 7.420886955069779, 1.8209106095604752, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(467025, 'HP:0007592', 'Aplasia/Hypoplastia of the eccrine sweat glands', 'XPO:0102840', 'abnormal stratum spongiosum morphology', 0.42, 7.420886955069779, 1.7654383368244009, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(467026, 'HP:0031980', 'Abnormal urine carboxylic acid level', 'XPO:0100069', 'abnormal urinary system', 0.4838709677419355, 6.355235291121788, 1.7536002539184354, 'HP:0000079', 'Abnormality of the urinary system'),
(467027, 'HP:0031980', 'Abnormal urine carboxylic acid level', 'XPO:0100501', 'abnormal urogenital system', 0.43333333333333335, 5.4478002382576385, 1.5364613358553185, 'HP:0000119', 'Abnormality of the genitourinary system'),
(467028, 'HP:0031980', 'Abnormal urine carboxylic acid level', 'XPO:0100085', 'abnormal mesonephric sinus', 0.4166666666666667, 6.355235291121788, 1.6272721667361236, 'HP:0000079', 'Abnormality of the urinary system'),
(467029, 'HP:0031980', 'Abnormal urine carboxylic acid level', 'XPO:0101701', 'abnormal urinary system morphology', 0.41025641025641024, 6.355235291121788, 1.61470617044417, 'HP:0000079', 'Abnormality of the urinary system'),
(467030, 'HP:0031980', 'Abnormal urine carboxylic acid level', 'XPO:0126535', 'abnormally localised urinary system', 0.41025641025641024, 6.355235291121788, 1.61470617044417, 'HP:0000079', 'Abnormality of the urinary system'),
(467031, 'HP:0030464', 'Asymmetrical distribution of pattern reversal visual evoked potentials', 'XPO:0101578', 'abnormal pupil', 0.40384615384615385, 6.02624522851634, 1.560024345217106, 'HP:0000478', 'Abnormality of the eye'),
(467032, 'HP:0030464', 'Asymmetrical distribution of pattern reversal visual evoked potentials', 'XPO:0100485', 'abnormal retina', 0.4117647058823529, 6.02624522851634, 1.5752444553449358, 'HP:0000478', 'Abnormality of the eye'),
(467033, 'HP:0030464', 'Asymmetrical distribution of pattern reversal visual evoked potentials', 'XPO:0100564', 'abnormal central retina', 0.40384615384615385, 6.02624522851634, 1.560024345217106, 'HP:0000478', 'Abnormality of the eye'),
(467034, 'HP:0030464', 'Asymmetrical distribution of pattern reversal visual evoked potentials', 'XPO:0101173', 'abnormal retinal layer', 0.44680851063829785, 6.02624522851634, 1.6409075706128409, 'HP:0000478', 'Abnormality of the eye'),
(467035, 'HP:0030464', 'Asymmetrical distribution of pattern reversal visual evoked potentials', 'XPO:0100918', 'abnormal lens', 0.4117647058823529, 6.02624522851634, 1.5752444553449358, 'HP:0000478', 'Abnormality of the eye'),
(467036, 'HP:0030464', 'Asymmetrical distribution of pattern reversal visual evoked potentials', 'XPO:0101554', 'abnormal peripheral retina', 0.40384615384615385, 6.02624522851634, 1.560024345217106, 'HP:0000478', 'Abnormality of the eye'),
(467037, 'HP:0030464', 'Asymmetrical distribution of pattern reversal visual evoked potentials', 'XPO:0100881', 'abnormal sclera', 0.4117647058823529, 6.02624522851634, 1.5752444553449358, 'HP:0000478', 'Abnormality of the eye'),
(467038, 'HP:0030464', 'Asymmetrical distribution of pattern reversal visual evoked potentials', 'XPO:0101416', 'abnormal cornea', 0.40384615384615385, 6.02624522851634, 1.560024345217106, 'HP:0000478', 'Abnormality of the eye'),
(467039, 'HP:0031060', 'Impaired ability to dress oneself', 'XPO:0141790', 'abnormal cellular metabolic process', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(467040, 'HP:0031060', 'Impaired ability to dress oneself', 'XPO:0100218', 'abnormal epithelial cell', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(467041, 'HP:0031060', 'Impaired ability to dress oneself', 'XPO:0101264', 'abnormal mitotic spindle', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(467042, 'HP:0031060', 'Impaired ability to dress oneself', 'XPO:0100515', 'abnormal somatic stem cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(467043, 'HP:0031060', 'Impaired ability to dress oneself', 'XPO:0107253', 'abnormal enteric nervous system', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(467044, 'HP:0031060', 'Impaired ability to dress oneself', 'XPO:0100010', 'abnormal multicellular anatomical structure', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(467045, 'HP:0031060', 'Impaired ability to dress oneself', 'XPO:0100422', 'abnormal notochord', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(467046, 'HP:0031060', 'Impaired ability to dress oneself', 'XPO:0100437', 'abnormal proepicardium', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(467047, 'HP:0031060', 'Impaired ability to dress oneself', 'XPO:0107259', 'abnormal animal-vegetal axis', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(467048, 'HP:0031060', 'Impaired ability to dress oneself', 'XPO:0141776', 'abnormal metabolic process', 0.5263157894736842, 1.8210412618256888, 0.9790009036675816, 'HP:0000118', 'Phenotypic abnormality'),
(467049, 'HP:0031060', 'Impaired ability to dress oneself', 'XPO:0141795', 'abnormal glycosylation', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(467050, 'HP:0031060', 'Impaired ability to dress oneself', 'XPO:0100392', 'abnormal cilium', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(467051, 'HP:0031060', 'Impaired ability to dress oneself', 'XPO:0100802', 'abnormal exocrine cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(467052, 'HP:0031060', 'Impaired ability to dress oneself', 'XPO:0107276', 'abnormal dorsal region', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(467053, 'HP:0031060', 'Impaired ability to dress oneself', 'XPO:0100014', 'abnormal tissue', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(467054, 'HP:0031060', 'Impaired ability to dress oneself', 'XPO:0100626', 'abnormal primordial germ cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(467055, 'HP:0031060', 'Impaired ability to dress oneself', 'XPO:0100427', 'abnormal olfactory system', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(467056, 'HP:0031060', 'Impaired ability to dress oneself', 'XPO:0100724', 'abnormal kinetochore', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(467057, 'HP:0031060', 'Impaired ability to dress oneself', 'XPO:0100006', 'abnormal anatomical structure', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(467058, 'HP:0031060', 'Impaired ability to dress oneself', 'XPO:0100337', 'abnormal zygote', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(467059, 'HP:0031060', 'Impaired ability to dress oneself', 'XPO:0131725', 'abnormal phosphorylation of RNA polymerase II C-terminal domain', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(467060, 'HP:0031060', 'Impaired ability to dress oneself', 'XPO:0100003', 'abnormal organism subdivision', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(467061, 'HP:0031060', 'Impaired ability to dress oneself', 'XPO:0141781', 'abnormal secondary metabolic process', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(467062, 'HP:0031060', 'Impaired ability to dress oneself', 'XPO:0116433', 'abnormal axis specification', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(467063, 'HP:0031060', 'Impaired ability to dress oneself', 'XPO:0101535', 'abnormal absorptive cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(467064, 'HP:0031060', 'Impaired ability to dress oneself', 'XPO:0101072', 'abnormal mitochondrial cloud', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(467065, 'HP:0031060', 'Impaired ability to dress oneself', 'XPO:0141911', 'abnormal ribose phosphate metabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(467066, 'HP:0031060', 'Impaired ability to dress oneself', 'XPO:0101228', 'abnormal mesenchymal stem cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(467067, 'HP:0031060', 'Impaired ability to dress oneself', 'XPO:0100728', 'abnormal cell condensation', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(467068, 'HP:0031060', 'Impaired ability to dress oneself', 'XPO:0101283', 'abnormal left-ventral blastomere', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(467069, 'HP:0031060', 'Impaired ability to dress oneself', 'XPO:0100642', 'abnormal gustatory system', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(467070, 'HP:0031060', 'Impaired ability to dress oneself', 'XPO:0128000', 'absent behavior', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(467071, 'HP:0031060', 'Impaired ability to dress oneself', 'XPO:0100377', 'abnormal connective tissue', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(467072, 'HP:0031060', 'Impaired ability to dress oneself', 'XPO:0101200', 'abnormal joint region', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(467073, 'HP:0031060', 'Impaired ability to dress oneself', 'XPO:0100894', 'abnormal nucleus', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(467074, 'HP:0031060', 'Impaired ability to dress oneself', 'XPO:0100917', 'abnormal stage III oocyte', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(467075, 'HP:0031060', 'Impaired ability to dress oneself', 'XPO:0101110', 'abnormal cell-free extract', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(467076, 'HP:0031060', 'Impaired ability to dress oneself', 'XPO:0100715', 'abnormal ciliated cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(467077, 'HP:0031060', 'Impaired ability to dress oneself', 'XPO:0100031', 'abnormal central nervous system', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(467078, 'HP:0031060', 'Impaired ability to dress oneself', 'XPO:0100026', 'abnormal germ cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(467079, 'HP:0031060', 'Impaired ability to dress oneself', 'XPO:0100721', 'abnormal centromere', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(467080, 'HP:0031060', 'Impaired ability to dress oneself', 'XPO:0101547', 'abnormal lampbrush chromosome', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(467081, 'HP:0031060', 'Impaired ability to dress oneself', 'XPO:0141775', 'abnormal nitrogen compound metabolic process', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(467082, 'HP:0031060', 'Impaired ability to dress oneself', 'XPO:0115508', 'abnormally peramorphic growth of whole organism', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(467083, 'HP:0031060', 'Impaired ability to dress oneself', 'XPO:0131469', 'abnormal heart process', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(467084, 'HP:0031060', 'Impaired ability to dress oneself', 'XPO:0116494', 'absent biological process', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(467085, 'HP:0031060', 'Impaired ability to dress oneself', 'XPO:0100969', 'abnormal disaggregated/reaggregated ectoderm treated with activin', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(467086, 'HP:0031060', 'Impaired ability to dress oneself', 'XPO:0100225', 'abnormal endocrine system', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(467087, 'HP:0031060', 'Impaired ability to dress oneself', 'XPO:0100643', 'abnormal thoracic region', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(467088, 'HP:0031060', 'Impaired ability to dress oneself', 'XPO:0100665', 'abnormal egg jelly', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(467089, 'HP:0031060', 'Impaired ability to dress oneself', 'XPO:0101132', 'abnormal apoptotic cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(467090, 'HP:0031060', 'Impaired ability to dress oneself', 'XPO:0101297', 'abnormal barrier cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(467091, 'HP:0031060', 'Impaired ability to dress oneself', 'XPO:0101468', 'abnormal stage I oocyte', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(467092, 'HP:0031060', 'Impaired ability to dress oneself', 'XPO:0107284', 'abnormal migrating myoblast', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(467093, 'HP:0031060', 'Impaired ability to dress oneself', 'XPO:0141743', 'abnormal chemical homeostasis within a tissue', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(467094, 'HP:0031060', 'Impaired ability to dress oneself', 'XPO:0100545', 'abnormal male organism', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(467095, 'HP:0031060', 'Impaired ability to dress oneself', 'XPO:0131740', 'abnormal detection of nodal flow', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(467096, 'HP:0031060', 'Impaired ability to dress oneself', 'XPO:0100704', 'abnormal Merkel cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(467097, 'HP:0031060', 'Impaired ability to dress oneself', 'XPO:0107270', 'abnormal proximal-distal axis', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(467098, 'HP:0031060', 'Impaired ability to dress oneself', 'XPO:0115512', 'abnormally semi-erect whole organism', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(467099, 'HP:0031060', 'Impaired ability to dress oneself', 'XPO:0141797', 'abnormal hydrogen metabolic process', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(467100, 'HP:0031060', 'Impaired ability to dress oneself', 'XPO:0100108', 'abnormal cell part', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(467101, 'HP:0031060', 'Impaired ability to dress oneself', 'XPO:0141892', 'abnormal inositol metabolic process', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(467102, 'HP:0031060', 'Impaired ability to dress oneself', 'XPO:0141771', 'abnormal urea homeostasis', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(467103, 'HP:0031060', 'Impaired ability to dress oneself', 'XPO:0133340', 'abnormal cell adhesion', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(467104, 'HP:0031060', 'Impaired ability to dress oneself', 'XPO:0141778', 'abnormal biosynthetic process', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(467105, 'HP:0031060', 'Impaired ability to dress oneself', 'XPO:0100084', 'abnormal anatomical group', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(467106, 'HP:0031060', 'Impaired ability to dress oneself', 'XPO:0100902', 'abnormal spermatocyte', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(467107, 'HP:0031060', 'Impaired ability to dress oneself', 'XPO:0141315', 'abnormal anatomical region', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(467108, 'HP:0031060', 'Impaired ability to dress oneself', 'XPO:0141772', 'abnormal water homeostasis', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(467109, 'HP:0031060', 'Impaired ability to dress oneself', 'XPO:0100176', 'abnormal stage VI oocyte', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(467110, 'HP:0031060', 'Impaired ability to dress oneself', 'XPO:0141798', 'abnormal lipid metabolic process', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(467111, 'HP:0031060', 'Impaired ability to dress oneself', 'XPO:0100754', 'abnormal electrically active cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(467112, 'HP:0031060', 'Impaired ability to dress oneself', 'XPO:0131691', 'abnormal molecular function', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(467113, 'HP:0031060', 'Impaired ability to dress oneself', 'XPO:0101347', 'abnormal hindlimb region', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(467114, 'HP:0031060', 'Impaired ability to dress oneself', 'XPO:0131667', 'abnormal actin cytoskeleton', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(467115, 'HP:0031060', 'Impaired ability to dress oneself', 'XPO:0141960', 'absent cilium motility in brain', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(467116, 'HP:0031060', 'Impaired ability to dress oneself', 'XPO:0101411', 'abnormal marginal zone (sensu neural)', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(467117, 'HP:0031060', 'Impaired ability to dress oneself', 'XPO:0107312', 'abnormal filopodium', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(467118, 'HP:0031060', 'Impaired ability to dress oneself', 'XPO:0100285', 'abnormal progenitor cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(467119, 'HP:0031060', 'Impaired ability to dress oneself', 'XPO:0141724', 'abnormal prevention of polyspermy', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(467120, 'HP:0031060', 'Impaired ability to dress oneself', 'XPO:0100070', 'abnormal anatomical system', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(467121, 'HP:0031060', 'Impaired ability to dress oneself', 'XPO:0101141', 'abnormal Keller explant', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(467122, 'HP:0031060', 'Impaired ability to dress oneself', 'XPO:0100899', 'abnormal secondary spermatogonium', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(467123, 'HP:0031060', 'Impaired ability to dress oneself', 'XPO:0141272', 'absent surface breathing', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(467124, 'HP:0031060', 'Impaired ability to dress oneself', 'XPO:0141796', 'abnormal demethylation', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(467125, 'HP:0031060', 'Impaired ability to dress oneself', 'XPO:0100104', 'abnormal embryonic structure', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(467126, 'HP:0031060', 'Impaired ability to dress oneself', 'XPO:0116434', 'abnormal biological process', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(467127, 'HP:0031060', 'Impaired ability to dress oneself', 'XPO:0100503', 'abnormal blastomere D2', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(467128, 'HP:0031060', 'Impaired ability to dress oneself', 'XPO:0141777', 'abnormal catabolic process', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(467129, 'HP:0031060', 'Impaired ability to dress oneself', 'XPO:0141499', 'abnormal tadpole', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(467130, 'HP:0031060', 'Impaired ability to dress oneself', 'XPO:0100533', 'abnormal melanoblast', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(467131, 'HP:0031060', 'Impaired ability to dress oneself', 'XPO:0100956', 'abnormal centrosome', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(467132, 'HP:0031060', 'Impaired ability to dress oneself', 'XPO:0107278', 'abnormal medial region', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(467133, 'HP:0031060', 'Impaired ability to dress oneself', 'XPO:0141271', 'increased surface breathing', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(467134, 'HP:0031060', 'Impaired ability to dress oneself', 'XPO:0133401', 'absent determination of left/right symmetry in lateral plate mesoderm', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(467135, 'HP:0031060', 'Impaired ability to dress oneself', 'XPO:0100004', 'abnormal cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
