(404897, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0100721', 'abnormal centromere', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(404898, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0131667', 'abnormal actin cytoskeleton', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(404899, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0141497', 'abnormal lymphoblast', 0.4482758620689655, 5.64885357140806, 1.5913028324062968, 'HP:0002715', 'Abnormality of the immune system'),
(404900, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0100691', 'abnormal keratin accumulating cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(404901, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0100372', 'abnormal hematological system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(404902, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0100921', 'abnormal dorsal caudal lymphatic vessel', 0.59375, 8.696350005340756, 2.2723243200896905, 'HP:0100763', 'Abnormality of the lymphatic system'),
(404903, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0100324', 'abnormal intersomitic vessel', 0.5, 5.809304221129108, 1.7043039959363335, 'UPHENO:0002678', 'abnormal vasculature'),
(404904, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0101524', 'abnormal ventral blood island border', 0.43243243243243246, 5.809304221129108, 1.5849705218340364, 'UPHENO:0002678', 'abnormal vasculature'),
(404905, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0103083', 'abnormal dorsal lymph space morphology', 0.42424242424242425, 5.64885357140806, 1.548057923116778, 'HP:0002715', 'Abnormality of the immune system'),
(404906, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0101241', 'abnormal nucleate erythrocyte', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(404907, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0101083', 'abnormal T cell', 0.43333333333333335, 5.64885357140806, 1.5645563421015427, 'HP:0002715', 'Abnormality of the immune system'),
(404908, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0100197', 'abnormal subclavian vein', 0.4444444444444444, 5.809304221129108, 1.6068332169732154, 'UPHENO:0002678', 'abnormal vasculature'),
(404909, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0100549', 'abnormal mitotic cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(404910, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0100477', 'abnormal pericyte', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(404911, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0100723', 'abnormal lateral postcardinal vein', 0.4444444444444444, 5.809304221129108, 1.6068332169732154, 'UPHENO:0002678', 'abnormal vasculature'),
(404912, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0101145', 'abnormal maxillary artery', 0.41025641025641024, 5.809304221129108, 1.5437954190396599, 'UPHENO:0002678', 'abnormal vasculature'),
(404913, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0101217', 'abnormal tail vein', 0.4444444444444444, 5.809304221129108, 1.6068332169732154, 'UPHENO:0002678', 'abnormal vasculature'),
(404914, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0101132', 'abnormal apoptotic cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(404915, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0100337', 'abnormal zygote', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(404916, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0100938', 'abnormal duct of Cuvier', 0.47058823529411764, 5.809304221129108, 1.6534177396253542, 'UPHENO:0002678', 'abnormal vasculature'),
(404917, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0100943', 'abnormal caudal vein', 0.43243243243243246, 5.809304221129108, 1.5849705218340364, 'UPHENO:0002678', 'abnormal vasculature'),
(404918, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0101864', 'abnormal lymphatic system morphology', 0.42424242424242425, 5.64885357140806, 1.548057923116778, 'HP:0002715', 'Abnormality of the immune system'),
(404919, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0100026', 'abnormal germ cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(404920, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0100792', 'abnormal capillary', 0.5333333333333333, 5.809304221129108, 1.760197598169646, 'UPHENO:0002678', 'abnormal vasculature'),
(404921, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0101373', 'abnormal oxygen accumulating cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(404922, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0141622', 'metaplastic right lymph heart', 0.42424242424242425, 5.64885357140806, 1.548057923116778, 'HP:0002715', 'Abnormality of the immune system'),
(404923, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0100148', 'abnormal arteria mesenterica posterior', 0.4444444444444444, 5.809304221129108, 1.6068332169732154, 'UPHENO:0002678', 'abnormal vasculature'),
(404924, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0100619', 'abnormal interrenal vein', 0.4444444444444444, 5.809304221129108, 1.6068332169732154, 'UPHENO:0002678', 'abnormal vasculature'),
(404925, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0100546', 'abnormal whole organism', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(404926, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0101240', 'abnormal ciliated non-epidermal cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(404927, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0100793', 'abnormal omphalomesenteric vein', 0.4444444444444444, 5.809304221129108, 1.6068332169732154, 'UPHENO:0002678', 'abnormal vasculature'),
(404928, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0100285', 'abnormal progenitor cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(404929, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0100789', 'abnormal occipitovertebral artery', 0.5161290322580645, 5.809304221129108, 1.731574591446772, 'UPHENO:0002678', 'abnormal vasculature'),
(404930, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0107312', 'abnormal filopodium', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(404931, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0100811', 'abnormal vena capitis medialis', 0.41025641025641024, 5.809304221129108, 1.5437954190396599, 'UPHENO:0002678', 'abnormal vasculature'),
(404932, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0100501', 'abnormal urogenital system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(404933, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0100080', 'abnormal aorta', 0.5161290322580645, 5.809304221129108, 1.731574591446772, 'UPHENO:0002678', 'abnormal vasculature'),
(404934, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0126796', 'abnormally localised dorsal longitudinal anastomosing vessel', 0.41025641025641024, 5.809304221129108, 1.5437954190396599, 'UPHENO:0002678', 'abnormal vasculature'),
(404935, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0100289', 'abnormal chondroblast', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(404936, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0101061', 'abnormal plasma membrane', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(404937, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0100079', 'abnormal dorsal aorta', 0.43243243243243246, 5.809304221129108, 1.5849705218340364, 'UPHENO:0002678', 'abnormal vasculature'),
(404938, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0101355', 'abnormal left omphalomesenteric vein', 0.42105263157894735, 5.809304221129108, 1.5639766078650594, 'UPHENO:0002678', 'abnormal vasculature'),
(404939, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0100731', 'abnormal arterial endothelium', 0.4444444444444444, 5.809304221129108, 1.6068332169732154, 'UPHENO:0002678', 'abnormal vasculature'),
(404940, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0101467', 'abnormal alkali secreting cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(404941, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0127928', 'abnormally localised dorsal caudal lymphatic vessel', 0.4523809523809524, 8.696350005340756, 1.9834472762476323, 'HP:0100763', 'Abnormality of the lymphatic system'),
(404942, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0101077', 'abnormal ventral abdominal vein', 0.4444444444444444, 5.809304221129108, 1.6068332169732154, 'UPHENO:0002678', 'abnormal vasculature'),
(404943, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0100754', 'abnormal electrically active cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(404944, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0100638', 'abnormal polar body', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(404945, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0100679', 'abnormal left channel of ventral aorta', 0.4444444444444444, 5.809304221129108, 1.6068332169732154, 'UPHENO:0002678', 'abnormal vasculature'),
(404946, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0100004', 'abnormal cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(404947, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0101029', 'abnormal right spleen primordium', 0.4482758620689655, 5.64885357140806, 1.5913028324062968, 'HP:0002715', 'Abnormality of the immune system'),
(404948, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0101206', 'abnormal ischiadic vein', 0.5161290322580645, 5.809304221129108, 1.731574591446772, 'UPHENO:0002678', 'abnormal vasculature'),
(404949, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0101518', 'abnormal B cell', 0.43333333333333335, 5.64885357140806, 1.5645563421015427, 'HP:0002715', 'Abnormality of the immune system'),
(404950, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0100653', 'abnormal myoblast', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(404951, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0101451', 'abnormal dorsal lymph space', 0.48148148148148145, 5.64885357140806, 1.6491871895674883, 'HP:0002715', 'Abnormality of the immune system'),
(404952, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0126460', 'abnormally localised artery', 0.41025641025641024, 5.809304221129108, 1.5437954190396599, 'UPHENO:0002678', 'abnormal vasculature'),
(404953, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0101369', 'abnormal nasociliary artery', 0.41025641025641024, 5.809304221129108, 1.5437954190396599, 'UPHENO:0002678', 'abnormal vasculature'),
(404954, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0100172', 'abnormal stem cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(404955, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0100802', 'abnormal exocrine cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(404956, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0100025', 'abnormal oocyte', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(404957, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0102554', 'abnormal lymph vessel morphology', 0.41304347826086957, 8.696350005340756, 1.8952494966045705, 'HP:0100763', 'Abnormality of the lymphatic system'),
(404958, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0127401', 'abnormally localised vascular plexus', 0.41025641025641024, 5.809304221129108, 1.5437954190396599, 'UPHENO:0002678', 'abnormal vasculature'),
(404959, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0100976', 'abnormal multiciliated cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(404960, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0100006', 'abnormal anatomical structure', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(404961, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0101051', 'abnormal intersomitic vein', 0.48484848484848486, 5.809304221129108, 1.6782825595347035, 'UPHENO:0002678', 'abnormal vasculature'),
(404962, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0101583', 'abnormal truncus arteriosus', 0.5333333333333333, 5.809304221129108, 1.760197598169646, 'UPHENO:0002678', 'abnormal vasculature'),
(404963, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0101371', 'abnormal facial vein', 0.41025641025641024, 5.809304221129108, 1.5437954190396599, 'UPHENO:0002678', 'abnormal vasculature'),
(404964, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0101004', 'abnormal acid secreting cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(404965, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0100323', 'abnormal intersomitic artery', 0.47058823529411764, 5.809304221129108, 1.6534177396253542, 'UPHENO:0002678', 'abnormal vasculature'),
(404966, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0100108', 'abnormal cell part', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(404967, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0100092', 'abnormal venous endothelium', 0.4444444444444444, 5.809304221129108, 1.6068332169732154, 'UPHENO:0002678', 'abnormal vasculature'),
(404968, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0101459', 'abnormal arteria iliaca communis', 0.4444444444444444, 5.809304221129108, 1.6068332169732154, 'UPHENO:0002678', 'abnormal vasculature'),
(404969, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0101585', 'abnormal dorsal longitudinal anastomosing vessel - right branch', 0.5161290322580645, 5.809304221129108, 1.731574591446772, 'UPHENO:0002678', 'abnormal vasculature'),
(404970, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0101110', 'abnormal cell-free extract', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(404971, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0101228', 'abnormal mesenchymal stem cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(404972, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0100888', 'abnormal microtubule', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(404973, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0100032', 'abnormal nervous system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(404974, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0101141', 'abnormal Keller explant', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(404975, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0101513', 'abnormal basal body', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(404976, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0100112', 'abnormal fin vasculature', 0.41025641025641024, 5.809304221129108, 1.5437954190396599, 'UPHENO:0002678', 'abnormal vasculature'),
(404977, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0101333', 'abnormal barrier epithelial cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(404978, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0126730', 'abnormally localised immune system', 0.42424242424242425, 5.64885357140806, 1.548057923116778, 'HP:0002715', 'Abnormality of the immune system'),
(404979, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0100489', 'abnormal vitelline vein', 0.4444444444444444, 5.809304221129108, 1.6068332169732154, 'UPHENO:0002678', 'abnormal vasculature'),
(404980, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0126365', 'abnormally localised vein', 0.41025641025641024, 5.809304221129108, 1.5437954190396599, 'UPHENO:0002678', 'abnormal vasculature'),
(404981, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0101080', 'abnormal posterior cardinal vein', 0.43243243243243246, 5.809304221129108, 1.5849705218340364, 'UPHENO:0002678', 'abnormal vasculature'),
(404982, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0100442', 'abnormal internal carotid artery', 0.41025641025641024, 5.809304221129108, 1.5437954190396599, 'UPHENO:0002678', 'abnormal vasculature'),
(404983, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0107284', 'abnormal migrating myoblast', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(404984, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0100852', 'abnormal interdigital region', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(404985, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0101448', 'abnormal myelin accumulating cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(404986, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0127105', 'abnormally localised circulatory system', 0.4117647058823529, 5.249153838287537, 1.4701755971154233, 'UPHENO:0080362', 'abnormal cardiovascular system'),
(404987, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0125762', 'absent lymph vessel', 0.4523809523809524, 8.696350005340756, 1.9834472762476323, 'HP:0100763', 'Abnormality of the lymphatic system'),
(404988, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0127543', 'abnormally localised ventral caudal lymphatic vessel', 0.4523809523809524, 8.696350005340756, 1.9834472762476323, 'HP:0100763', 'Abnormality of the lymphatic system'),
(404989, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0100437', 'abnormal proepicardium', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(404990, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0100075', 'abnormal mandibular artery', 0.41025641025641024, 5.809304221129108, 1.5437954190396599, 'UPHENO:0002678', 'abnormal vasculature'),
(404991, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0126558', 'abnormally localised truncus arteriosus', 0.41025641025641024, 5.809304221129108, 1.5437954190396599, 'UPHENO:0002678', 'abnormal vasculature'),
(404992, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0101569', 'abnormal activin-induced ectoderm', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(404993, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0100933', 'abnormal branchial vein', 0.5161290322580645, 5.809304221129108, 1.731574591446772, 'UPHENO:0002678', 'abnormal vasculature'),
(404994, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0101580', 'abnormal cutaneous magnus', 0.4444444444444444, 5.809304221129108, 1.6068332169732154, 'UPHENO:0002678', 'abnormal vasculature'),
(404995, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0100053', 'abnormal head vasculature', 0.4444444444444444, 5.809304221129108, 1.6068332169732154, 'UPHENO:0002678', 'abnormal vasculature'),
(404996, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0125107', 'absent immune system', 0.4117647058823529, 5.64885357140806, 1.525122463739656, 'HP:0002715', 'Abnormality of the immune system'),
(404997, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0100814', 'abnormal natural killer cell', 0.41935483870967744, 5.64885357140806, 1.5391147060347428, 'HP:0002715', 'Abnormality of the immune system'),
(404998, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0100043', 'abnormal vein', 0.5333333333333333, 5.809304221129108, 1.760197598169646, 'UPHENO:0002678', 'abnormal vasculature'),
(404999, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0100704', 'abnormal Merkel cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(405000, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0141616', 'metaplastic left lymph heart', 0.42424242424242425, 5.64885357140806, 1.548057923116778, 'HP:0002715', 'Abnormality of the immune system'),
(405001, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0100801', 'abnormal vena capitis lateralis', 0.41025641025641024, 5.809304221129108, 1.5437954190396599, 'UPHENO:0002678', 'abnormal vasculature'),
(405002, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0101487', 'abnormal epigastric artery', 0.4444444444444444, 5.809304221129108, 1.6068332169732154, 'UPHENO:0002678', 'abnormal vasculature'),
(405003, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0100894', 'abnormal nucleus', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(405004, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0100745', 'abnormal anterior lymph sac', 0.4642857142857143, 5.64885357140806, 1.6194696710023933, 'HP:0002715', 'Abnormality of the immune system'),
(405005, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0100780', 'abnormal vascular plexus', 0.5333333333333333, 5.809304221129108, 1.760197598169646, 'UPHENO:0002678', 'abnormal vasculature'),
(405006, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0101557', 'abnormal Jacobsons vein', 0.5161290322580645, 5.809304221129108, 1.731574591446772, 'UPHENO:0002678', 'abnormal vasculature'),
(405007, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0100522', 'abnormal subinterstitial vein', 0.5161290322580645, 5.809304221129108, 1.731574591446772, 'UPHENO:0002678', 'abnormal vasculature'),
(405008, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0101013', 'abnormal ventral caudal lymphatic vessel', 0.59375, 8.696350005340756, 2.2723243200896905, 'HP:0100763', 'Abnormality of the lymphatic system'),
(405009, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0101243', 'abnormal vertebral artery', 0.5161290322580645, 5.809304221129108, 1.731574591446772, 'UPHENO:0002678', 'abnormal vasculature'),
(405010, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0101116', 'abnormal lateral vein', 0.4444444444444444, 5.809304221129108, 1.6068332169732154, 'UPHENO:0002678', 'abnormal vasculature'),
(405011, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0100242', 'abnormal right lymph heart', 0.43333333333333335, 5.64885357140806, 1.5645563421015427, 'HP:0002715', 'Abnormality of the immune system'),
(405012, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0127129', 'abnormally localised capillary', 0.41025641025641024, 5.809304221129108, 1.5437954190396599, 'UPHENO:0002678', 'abnormal vasculature'),
(405013, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0100137', 'abnormal cardinal vein', 0.5161290322580645, 5.809304221129108, 1.731574591446772, 'UPHENO:0002678', 'abnormal vasculature'),
(405014, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0100956', 'abnormal centrosome', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(405015, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0100626', 'abnormal primordial germ cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(405016, 'HP:0100763', 'Abnormality of the lymphatic system', 'XPO:0100488', 'abnormal external jugular vein', 0.41025641025641024, 5.809304221129108, 1.5437954190396599, 'UPHENO:0002678', 'abnormal vasculature'),
(405017, 'HP:0040022', 'Clinodactyly of the 2nd finger', 'XPO:0129161', 'decreased size of the forelimb digit 5', 0.42592592592592593, 7.492661022682715, 1.7864262043911108, 'HP:0001167', 'Abnormal finger morphology'),
(405018, 'HP:0040022', 'Clinodactyly of the 2nd finger', 'XPO:0130664', 'increased size of the forelimb digit 2', 0.42990654205607476, 7.492661022682715, 1.7947545768321247, 'HP:0001167', 'Abnormal finger morphology'),
(405019, 'HP:0040022', 'Clinodactyly of the 2nd finger', 'XPO:0102529', 'abnormal forelimb digit 4 morphology', 0.4791666666666667, 7.492661022682715, 1.8947911248214497, 'HP:0001167', 'Abnormal finger morphology'),
(405020, 'HP:0040022', 'Clinodactyly of the 2nd finger', 'XPO:0129652', 'increased size of the forelimb digit 3', 0.42990654205607476, 7.492661022682715, 1.7947545768321247, 'HP:0001167', 'Abnormal finger morphology'),
(405021, 'HP:0040022', 'Clinodactyly of the 2nd finger', 'XPO:0141556', 'abnormal forelimb digit morphology in the regenerating forelimb', 0.46, 7.492661022682715, 1.8565085699866966, 'HP:0001167', 'Abnormal finger morphology'),
(405022, 'HP:0040022', 'Clinodactyly of the 2nd finger', 'XPO:0133378', 'fused forelimb digits part of regenerating forelimb', 0.41818181818181815, 7.492661022682715, 1.7701114680961476, 'HP:0001167', 'Abnormal finger morphology'),
(405023, 'HP:0040022', 'Clinodactyly of the 2nd finger', 'XPO:0102214', 'abnormal forelimb digit morphology', 0.48936170212765956, 7.492661022682715, 1.914842382945809, 'HP:0001167', 'Abnormal finger morphology'),
(405024, 'HP:0040022', 'Clinodactyly of the 2nd finger', 'XPO:0140898', 'abnormally necrotic forelimb digit 5', 0.4380952380952381, 7.492661022682715, 1.8117668488795942, 'HP:0001167', 'Abnormal finger morphology'),
(405025, 'HP:0040022', 'Clinodactyly of the 2nd finger', 'XPO:0133358', 'fused forelimb digits', 0.44660194174757284, 7.492661022682715, 1.829272249170816, 'HP:0001167', 'Abnormal finger morphology'),
(405026, 'HP:0040022', 'Clinodactyly of the 2nd finger', 'XPO:0103755', 'increased size of the forelimb digit', 0.4423076923076923, 7.492661022682715, 1.820456427983539, 'HP:0001167', 'Abnormal finger morphology'),
(405027, 'HP:0040022', 'Clinodactyly of the 2nd finger', 'XPO:0103465', 'bifurcated forelimb digit 2', 0.40707964601769914, 7.492661022682715, 1.7464563541194758, 'HP:0001167', 'Abnormal finger morphology'),
(405028, 'HP:0040022', 'Clinodactyly of the 2nd finger', 'XPO:0103467', 'bifurcated forelimb digit 4', 0.40707964601769914, 7.492661022682715, 1.7464563541194758, 'HP:0001167', 'Abnormal finger morphology'),
(405029, 'HP:0040022', 'Clinodactyly of the 2nd finger', 'XPO:0129148', 'decreased size of the forelimb digit 4', 0.42592592592592593, 7.492661022682715, 1.7864262043911108, 'HP:0001167', 'Abnormal finger morphology'),
(405030, 'HP:0040022', 'Clinodactyly of the 2nd finger', 'XPO:0130624', 'increased size of the forelimb digit 4', 0.42990654205607476, 7.492661022682715, 1.7947545768321247, 'HP:0001167', 'Abnormal finger morphology'),
(405031, 'HP:0040022', 'Clinodactyly of the 2nd finger', 'XPO:0101810', 'abnormal digit morphology', 0.425, 6.466375519622663, 1.657772480118919, 'UPHENO:0086700', 'abnormal digit morphology'),
(405032, 'HP:0040022', 'Clinodactyly of the 2nd finger', 'XPO:0128172', 'decreased size of the forelimb digit 3', 0.42592592592592593, 7.492661022682715, 1.7864262043911108, 'HP:0001167', 'Abnormal finger morphology'),
(405033, 'HP:0040022', 'Clinodactyly of the 2nd finger', 'XPO:0140219', 'abnormally necrotic forelimb digit', 0.45098039215686275, 7.492661022682715, 1.8382173990874668, 'HP:0001167', 'Abnormal finger morphology'),
(405034, 'HP:0040022', 'Clinodactyly of the 2nd finger', 'XPO:0103432', 'decreased size of the forelimb digit', 0.4380952380952381, 7.492661022682715, 1.8117668488795942, 'HP:0001167', 'Abnormal finger morphology'),
(405035, 'HP:0040022', 'Clinodactyly of the 2nd finger', 'XPO:0130637', 'increased size of the forelimb digit 5', 0.42990654205607476, 7.492661022682715, 1.7947545768321247, 'HP:0001167', 'Abnormal finger morphology'),
(405036, 'HP:0040022', 'Clinodactyly of the 2nd finger', 'XPO:0102787', 'abnormal forelimb digit 5 morphology', 0.4791666666666667, 7.492661022682715, 1.8947911248214497, 'HP:0001167', 'Abnormal finger morphology'),
(405037, 'HP:0040022', 'Clinodactyly of the 2nd finger', 'XPO:0129188', 'decreased size of the forelimb digit 2', 0.42592592592592593, 7.492661022682715, 1.7864262043911108, 'HP:0001167', 'Abnormal finger morphology'),
(405038, 'HP:0040022', 'Clinodactyly of the 2nd finger', 'XPO:0141108', 'abnormally necrotic forelimb digit 2', 0.4380952380952381, 7.492661022682715, 1.8117668488795942, 'HP:0001167', 'Abnormal finger morphology'),
(405039, 'HP:0040022', 'Clinodactyly of the 2nd finger', 'XPO:0103468', 'bifurcated forelimb digit 5', 0.40707964601769914, 7.492661022682715, 1.7464563541194758, 'HP:0001167', 'Abnormal finger morphology'),
(405040, 'HP:0040022', 'Clinodactyly of the 2nd finger', 'XPO:0103779', 'decreased size of the forelimb digit in the regenerating forelimb', 0.4107142857142857, 7.492661022682715, 1.7542357082303395, 'HP:0001167', 'Abnormal finger morphology'),
(405041, 'HP:0040022', 'Clinodactyly of the 2nd finger', 'XPO:0140716', 'abnormally necrotic forelimb digit 4', 0.4380952380952381, 7.492661022682715, 1.8117668488795942, 'HP:0001167', 'Abnormal finger morphology'),
(405042, 'HP:0040022', 'Clinodactyly of the 2nd finger', 'XPO:0141143', 'abnormally necrotic forelimb digit 3', 0.4380952380952381, 7.492661022682715, 1.8117668488795942, 'HP:0001167', 'Abnormal finger morphology'),
(405043, 'HP:0040022', 'Clinodactyly of the 2nd finger', 'XPO:0102598', 'abnormal forelimb digit 3 morphology', 0.4791666666666667, 7.492661022682715, 1.8947911248214497, 'HP:0001167', 'Abnormal finger morphology'),
(405044, 'HP:0040022', 'Clinodactyly of the 2nd finger', 'XPO:0103466', 'bifurcated forelimb digit 3', 0.40707964601769914, 7.492661022682715, 1.7464563541194758, 'HP:0001167', 'Abnormal finger morphology'),
(405045, 'HP:0040022', 'Clinodactyly of the 2nd finger', 'XPO:0102746', 'abnormal forelimb digit 2 morphology', 0.4791666666666667, 7.492661022682715, 1.8947911248214497, 'HP:0001167', 'Abnormal finger morphology'),
(405046, 'HP:0040022', 'Clinodactyly of the 2nd finger', 'XPO:0141208', 'abnormally necrotic digit-joint region', 0.40476190476190477, 6.466375519622663, 1.617820284280124, 'UPHENO:0086700', 'abnormal digit morphology'),
(405047, 'HP:0040022', 'Clinodactyly of the 2nd finger', 'XPO:0125257', 'absent forelimb digit', 0.40350877192982454, 7.492661022682715, 1.7387795857293602, 'HP:0001167', 'Abnormal finger morphology'),
(405048, 'HP:0040022', 'Clinodactyly of the 2nd finger', 'XPO:0102880', 'abnormal digit-joint region morphology', 0.425, 6.466375519622663, 1.657772480118919, 'UPHENO:0086700', 'abnormal digit morphology'),
(405049, 'HP:0032792', 'Tonic seizure', 'XPO:0100858', 'abnormal presumptive midbrain-hindbrain boundary', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(405050, 'HP:0032792', 'Tonic seizure', 'XPO:0142051', 'abnormal cerebrospinal fluid', 0.43333333333333335, 3.94131651835137, 1.3068679445984308, 'UPHENO:0004523', 'abnormal nervous system'),
(405051, 'HP:0032792', 'Tonic seizure', 'XPO:0100916', 'abnormal principal cavity', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(405052, 'HP:0032792', 'Tonic seizure', 'XPO:0100760', 'abnormal Stirnorgan', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(405053, 'HP:0032792', 'Tonic seizure', 'XPO:0100164', 'abnormal neural nucleus', 0.43333333333333335, 3.94131651835137, 1.3068679445984308, 'UPHENO:0004523', 'abnormal nervous system'),
(405054, 'HP:0032792', 'Tonic seizure', 'XPO:0107253', 'abnormal enteric nervous system', 0.4642857142857143, 3.94131651835137, 1.3527368387638634, 'UPHENO:0004523', 'abnormal nervous system'),
(405055, 'HP:0032792', 'Tonic seizure', 'XPO:0100702', 'abnormal glial cell', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(405056, 'HP:0032792', 'Tonic seizure', 'XPO:0100734', 'abnormal lateral line system', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(405057, 'HP:0032792', 'Tonic seizure', 'XPO:0100537', 'abnormal medium cavity', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(405058, 'HP:0032792', 'Tonic seizure', 'XPO:0101133', 'abnormal motor neuron', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(405059, 'HP:0032792', 'Tonic seizure', 'XPO:0100031', 'abnormal central nervous system', 0.4642857142857143, 3.94131651835137, 1.3527368387638634, 'UPHENO:0004523', 'abnormal nervous system'),
(405060, 'HP:0032792', 'Tonic seizure', 'XPO:0100587', 'abnormal vestibuloauditory system', 0.4482758620689655, 3.94131651835137, 1.3292091859262085, 'UPHENO:0004523', 'abnormal nervous system'),
(405061, 'HP:0032792', 'Tonic seizure', 'XPO:0100196', 'abnormal neuron', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(405062, 'HP:0032792', 'Tonic seizure', 'XPO:0100114', 'abnormal peripheral nervous system', 0.43333333333333335, 3.94131651835137, 1.3068679445984308, 'UPHENO:0004523', 'abnormal nervous system'),
(405063, 'HP:0032792', 'Tonic seizure', 'XPO:0100701', 'abnormal microglial cell', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(405064, 'HP:0032792', 'Tonic seizure', 'XPO:0100032', 'abnormal nervous system', 0.48148148148148145, 3.94131651835137, 1.3775597686645948, 'UPHENO:0004523', 'abnormal nervous system'),
(405065, 'HP:0032792', 'Tonic seizure', 'XPO:0100864', 'abnormal dorsolateral ascending neuron', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(405066, 'HP:0032792', 'Tonic seizure', 'XPO:0100158', 'abnormal neuromere', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(405067, 'HP:0032792', 'Tonic seizure', 'XPO:0101501', 'abnormal parabrachial area', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(405068, 'HP:0032792', 'Tonic seizure', 'XPO:0100004', 'abnormal cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(405069, 'HP:0032792', 'Tonic seizure', 'XPO:0100642', 'abnormal gustatory system', 0.4482758620689655, 3.94131651835137, 1.3292091859262085, 'UPHENO:0004523', 'abnormal nervous system'),
(405070, 'HP:0032792', 'Tonic seizure', 'XPO:0101187', 'abnormal dorsolateral commissural neuron', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(405071, 'HP:0032792', 'Tonic seizure', 'XPO:0100274', 'abnormal sensory system', 0.4642857142857143, 3.94131651835137, 1.3527368387638634, 'UPHENO:0004523', 'abnormal nervous system'),
(405072, 'HP:0032792', 'Tonic seizure', 'XPO:0100954', 'abnormal neural progenitor cell', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(405073, 'HP:0032792', 'Tonic seizure', 'XPO:0100273', 'abnormal visual system', 0.4482758620689655, 3.94131651835137, 1.3292091859262085, 'UPHENO:0004523', 'abnormal nervous system'),
(405074, 'HP:0032792', 'Tonic seizure', 'XPO:0100427', 'abnormal olfactory system', 0.4482758620689655, 3.94131651835137, 1.3292091859262085, 'UPHENO:0004523', 'abnormal nervous system'),
(405075, 'HP:0032792', 'Tonic seizure', 'XPO:0100175', 'abnormal migrating neuroblast', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(405076, 'HP:0034258', 'Aplasia/Hypoplasia of the midbrain', 'XPO:0142044', 'increased size of the cerebrospinal fluid', 0.42857142857142855, 5.483278994082134, 1.5329633758669794, 'HP:0002011', 'Morphological central nervous system abnormality'),
(405077, 'HP:0034258', 'Aplasia/Hypoplasia of the midbrain', 'XPO:0139757', 'abnormally necrotic neural nucleus', 0.4090909090909091, 5.483278994082134, 1.4977181271815287, 'HP:0002011', 'Morphological central nervous system abnormality'),
(405078, 'HP:0034258', 'Aplasia/Hypoplasia of the midbrain', 'XPO:0100114', 'abnormal peripheral nervous system', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(405079, 'HP:0034258', 'Aplasia/Hypoplasia of the midbrain', 'XPO:0142051', 'abnormal cerebrospinal fluid', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(405080, 'HP:0034258', 'Aplasia/Hypoplasia of the midbrain', 'XPO:0107340', 'abnormal enteric nervous system morphology', 0.42105263157894735, 4.7814666189787065, 1.4188900953660493, 'HP:0012639', 'Abnormal nervous system morphology'),
(405081, 'HP:0034258', 'Aplasia/Hypoplasia of the midbrain', 'XPO:0102548', 'abnormal principal cavity morphology', 0.41025641025641024, 4.7814666189787065, 1.4005810690078098, 'HP:0012639', 'Abnormal nervous system morphology'),
(405082, 'HP:0034258', 'Aplasia/Hypoplasia of the midbrain', 'XPO:0140468', 'abnormally necrotic central nervous system', 0.4090909090909091, 5.483278994082134, 1.4977181271815287, 'HP:0002011', 'Morphological central nervous system abnormality'),
(405083, 'HP:0034258', 'Aplasia/Hypoplasia of the midbrain', 'XPO:0100427', 'abnormal olfactory system', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(405084, 'HP:0034258', 'Aplasia/Hypoplasia of the midbrain', 'XPO:0142058', 'abnormal cerebrospinal fluid morphology', 0.4864864864864865, 5.483278994082134, 1.6332608892201435, 'HP:0002011', 'Morphological central nervous system abnormality'),
(405085, 'HP:0034258', 'Aplasia/Hypoplasia of the midbrain', 'XPO:0107253', 'abnormal enteric nervous system', 0.43333333333333335, 3.94131651835137, 1.3068679445984308, 'UPHENO:0004523', 'abnormal nervous system'),
(405086, 'HP:0034258', 'Aplasia/Hypoplasia of the midbrain', 'XPO:0102169', 'abnormal medium cavity morphology', 0.41025641025641024, 4.7814666189787065, 1.4005810690078098, 'HP:0012639', 'Abnormal nervous system morphology'),
(405087, 'HP:0034258', 'Aplasia/Hypoplasia of the midbrain', 'XPO:0102219', 'abnormal vestibuloauditory system morphology', 0.41025641025641024, 4.7814666189787065, 1.4005810690078098, 'HP:0012639', 'Abnormal nervous system morphology'),
(405088, 'HP:0034258', 'Aplasia/Hypoplasia of the midbrain', 'XPO:0100273', 'abnormal visual system', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(405089, 'HP:0034258', 'Aplasia/Hypoplasia of the midbrain', 'XPO:0100164', 'abnormal neural nucleus', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(405090, 'HP:0034258', 'Aplasia/Hypoplasia of the midbrain', 'XPO:0101905', 'abnormal visual system morphology', 0.41025641025641024, 4.7814666189787065, 1.4005810690078098, 'HP:0012639', 'Abnormal nervous system morphology'),
(405091, 'HP:0034258', 'Aplasia/Hypoplasia of the midbrain', 'XPO:0100587', 'abnormal vestibuloauditory system', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(405092, 'HP:0034258', 'Aplasia/Hypoplasia of the midbrain', 'XPO:0101790', 'abnormal neuromere morphology', 0.45, 5.483278994082134, 1.5708200238528156, 'HP:0002011', 'Morphological central nervous system abnormality'),
(405093, 'HP:0034258', 'Aplasia/Hypoplasia of the midbrain', 'XPO:0102490', 'abnormal presumptive midbrain-hindbrain boundary morphology', 0.42857142857142855, 5.483278994082134, 1.5329633758669794, 'HP:0002011', 'Morphological central nervous system abnormality'),
(405094, 'HP:0034258', 'Aplasia/Hypoplasia of the midbrain', 'XPO:0101906', 'abnormal sensory system morphology', 0.43243243243243246, 4.7814666189787065, 1.4379364522257028, 'HP:0012639', 'Abnormal nervous system morphology'),
(405095, 'HP:0034258', 'Aplasia/Hypoplasia of the midbrain', 'XPO:0142037', 'decreased size of the cerebrospinal fluid', 0.42857142857142855, 5.483278994082134, 1.5329633758669794, 'HP:0002011', 'Morphological central nervous system abnormality'),
(405096, 'HP:0034258', 'Aplasia/Hypoplasia of the midbrain', 'XPO:0100032', 'abnormal nervous system', 0.4482758620689655, 3.94131651835137, 1.3292091859262085, 'UPHENO:0004523', 'abnormal nervous system'),
(405097, 'HP:0034258', 'Aplasia/Hypoplasia of the midbrain', 'XPO:0103127', 'abnormal torus semicircularis morphology', 0.4074074074074074, 9.63462101558905, 1.9812157806039343, 'UPHENO:0076795', 'abnormal midbrain morphology'),
(405098, 'HP:0034258', 'Aplasia/Hypoplasia of the midbrain', 'XPO:0100031', 'abnormal central nervous system', 0.43333333333333335, 3.94131651835137, 1.3068679445984308, 'UPHENO:0004523', 'abnormal nervous system'),
(405099, 'HP:0034258', 'Aplasia/Hypoplasia of the midbrain', 'XPO:0103133', 'abnormal parabrachial area morphology', 0.43902439024390244, 5.483278994082134, 1.5515454285692403, 'HP:0002011', 'Morphological central nervous system abnormality'),
(405100, 'HP:0034258', 'Aplasia/Hypoplasia of the midbrain', 'XPO:0101972', 'abnormal midbrain morphology', 0.41509433962264153, 9.63462101558905, 1.9998191538187546, 'UPHENO:0076795', 'abnormal midbrain morphology'),
(405101, 'HP:0034258', 'Aplasia/Hypoplasia of the midbrain', 'XPO:0131746', 'abnormal neural tube closure', 0.43902439024390244, 5.483278994082134, 1.5515454285692403, 'HP:0002011', 'Morphological central nervous system abnormality'),
(405102, 'HP:0034258', 'Aplasia/Hypoplasia of the midbrain', 'XPO:0101796', 'abnormal neural nucleus morphology', 0.46153846153846156, 5.483278994082134, 1.5908312767590507, 'HP:0002011', 'Morphological central nervous system abnormality'),
(405103, 'HP:0034258', 'Aplasia/Hypoplasia of the midbrain', 'XPO:0100642', 'abnormal gustatory system', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(405104, 'HP:0034258', 'Aplasia/Hypoplasia of the midbrain', 'XPO:0101663', 'abnormal central nervous system morphology', 0.47368421052631576, 5.483278994082134, 1.6116273394948744, 'HP:0002011', 'Morphological central nervous system abnormality'),
(405105, 'HP:0034258', 'Aplasia/Hypoplasia of the midbrain', 'XPO:0101664', 'abnormal nervous system morphology', 0.4444444444444444, 4.7814666189787065, 1.4577709954247435, 'HP:0012639', 'Abnormal nervous system morphology'),
(405106, 'HP:0034258', 'Aplasia/Hypoplasia of the midbrain', 'XPO:0142031', 'abnormally necrotic cerebrospinal fluid', 0.45, 5.483278994082134, 1.5708200238528156, 'HP:0002011', 'Morphological central nervous system abnormality'),
(405107, 'HP:0034258', 'Aplasia/Hypoplasia of the midbrain', 'XPO:0100274', 'abnormal sensory system', 0.43333333333333335, 3.94131651835137, 1.3068679445984308, 'UPHENO:0004523', 'abnormal nervous system'),
(405108, 'HP:0006224', 'Tapering pointed ends of distal finger phalanges', 'XPO:0103634', 'abnormally increased number of forelimb digit', 0.47107438016528924, 7.774297771301195, 1.9137064831985338, 'HP:0005918', 'Abnormal finger phalanx morphology'),
(405109, 'HP:0006224', 'Tapering pointed ends of distal finger phalanges', 'XPO:0103467', 'bifurcated forelimb digit 4', 0.4146341463414634, 8.968875860151847, 1.928419608362407, 'UPHENO:0082301', 'shape anatomical entity in pectoral complex'),
(405110, 'HP:0006224', 'Tapering pointed ends of distal finger phalanges', 'XPO:0103465', 'bifurcated forelimb digit 2', 0.4146341463414634, 8.968875860151847, 1.928419608362407, 'UPHENO:0082301', 'shape anatomical entity in pectoral complex'),
(405111, 'HP:0006224', 'Tapering pointed ends of distal finger phalanges', 'XPO:0115786', 'duplicated forelimb digit 2 in regenerating forelimb', 0.4318181818181818, 7.774297771301195, 1.8322344633033256, 'HP:0005918', 'Abnormal finger phalanx morphology'),
(405112, 'HP:0006224', 'Tapering pointed ends of distal finger phalanges', 'XPO:0103468', 'bifurcated forelimb digit 5', 0.4146341463414634, 8.968875860151847, 1.928419608362407, 'UPHENO:0082301', 'shape anatomical entity in pectoral complex'),
(405113, 'HP:0006224', 'Tapering pointed ends of distal finger phalanges', 'XPO:0102214', 'abnormal forelimb digit morphology', 0.4351851851851852, 7.492661022682715, 1.8057394813997938, 'HP:0001167', 'Abnormal finger morphology'),
(405114, 'HP:0006224', 'Tapering pointed ends of distal finger phalanges', 'XPO:0115787', 'duplicated forelimb digit 3 in regenerating forelimb', 0.4318181818181818, 7.774297771301195, 1.8322344633033256, 'HP:0005918', 'Abnormal finger phalanx morphology'),
(405115, 'HP:0006224', 'Tapering pointed ends of distal finger phalanges', 'XPO:0141556', 'abnormal forelimb digit morphology in the regenerating forelimb', 0.41228070175438597, 7.492661022682715, 1.7575777491876043, 'HP:0001167', 'Abnormal finger morphology'),
(405116, 'HP:0006224', 'Tapering pointed ends of distal finger phalanges', 'XPO:0102787', 'abnormal forelimb digit 5 morphology', 0.42727272727272725, 7.492661022682715, 1.7892483644513149, 'HP:0001167', 'Abnormal finger morphology'),
(405117, 'HP:0006224', 'Tapering pointed ends of distal finger phalanges', 'XPO:0140219', 'abnormally necrotic forelimb digit', 0.4051724137931034, 7.492661022682715, 1.7423603393941962, 'HP:0001167', 'Abnormal finger morphology'),
(405118, 'HP:0006224', 'Tapering pointed ends of distal finger phalanges', 'XPO:0102598', 'abnormal forelimb digit 3 morphology', 0.42727272727272725, 7.492661022682715, 1.7892483644513149, 'HP:0001167', 'Abnormal finger morphology'),
(405119, 'HP:0006224', 'Tapering pointed ends of distal finger phalanges', 'XPO:0133358', 'fused forelimb digits', 0.4017094017094017, 7.492661022682715, 1.734898376457027, 'HP:0001167', 'Abnormal finger morphology'),
(405120, 'HP:0006224', 'Tapering pointed ends of distal finger phalanges', 'XPO:0102746', 'abnormal forelimb digit 2 morphology', 0.42727272727272725, 7.492661022682715, 1.7892483644513149, 'HP:0001167', 'Abnormal finger morphology'),
(405121, 'HP:0006224', 'Tapering pointed ends of distal finger phalanges', 'XPO:0102529', 'abnormal forelimb digit 4 morphology', 0.42727272727272725, 7.492661022682715, 1.7892483644513149, 'HP:0001167', 'Abnormal finger morphology'),
(405122, 'HP:0006224', 'Tapering pointed ends of distal finger phalanges', 'XPO:0115789', 'duplicated forelimb digit 5 in regenerating forelimb', 0.4318181818181818, 7.774297771301195, 1.8322344633033256, 'HP:0005918', 'Abnormal finger phalanx morphology'),
(405123, 'HP:0006224', 'Tapering pointed ends of distal finger phalanges', 'XPO:0103466', 'bifurcated forelimb digit 3', 0.4146341463414634, 8.968875860151847, 1.928419608362407, 'UPHENO:0082301', 'shape anatomical entity in pectoral complex'),
(405124, 'HP:0006224', 'Tapering pointed ends of distal finger phalanges', 'XPO:0103609', 'abnormally increased number of forelimb digit in the regenerating forelimb', 0.44881889763779526, 7.774297771301195, 1.8679538954758415, 'HP:0005918', 'Abnormal finger phalanx morphology'),
(405125, 'HP:0006224', 'Tapering pointed ends of distal finger phalanges', 'XPO:0115788', 'duplicated forelimb digit 4 in regenerating forelimb', 0.4318181818181818, 7.774297771301195, 1.8322344633033256, 'HP:0005918', 'Abnormal finger phalanx morphology'),
(405126, 'HP:0006763', 'Anal canal squamous carcinoma', 'XPO:0101288', 'abnormal external coil of the small intestine', 0.42857142857142855, 8.518562886125473, 1.9107099898944229, 'UPHENO:0076783', 'abnormal intestine morphology'),
(405127, 'HP:0006763', 'Anal canal squamous carcinoma', 'XPO:0101537', 'abnormal internal coil of the small intestine', 0.42857142857142855, 8.518562886125473, 1.9107099898944229, 'UPHENO:0076783', 'abnormal intestine morphology'),
(405128, 'HP:0006763', 'Anal canal squamous carcinoma', 'XPO:0100361', 'abnormal small intestine', 0.43636363636363634, 8.518562886125473, 1.928001835471643, 'UPHENO:0076783', 'abnormal intestine morphology'),
(405129, 'HP:0006763', 'Anal canal squamous carcinoma', 'XPO:0101471', 'abnormal rectum', 0.45614035087719296, 10.665155383737162, 2.2056309117569177, 'HP:0002250', 'Abnormal large intestine morphology'),
(405130, 'HP:0006763', 'Anal canal squamous carcinoma', 'XPO:0102473', 'abnormal large intestine morphology', 0.4262295081967213, 10.665155383737162, 2.1320891008707643, 'HP:0002250', 'Abnormal large intestine morphology'),
(405131, 'HP:0006763', 'Anal canal squamous carcinoma', 'XPO:0102941', 'abnormal colon morphology', 0.4126984126984127, 10.665155383737162, 2.0979734741054896, 'HP:0002250', 'Abnormal large intestine morphology'),
(405132, 'HP:0006763', 'Anal canal squamous carcinoma', 'XPO:0101321', 'abnormal duodenum', 0.42857142857142855, 8.518562886125473, 1.9107099898944229, 'UPHENO:0076783', 'abnormal intestine morphology'),
(405133, 'HP:0006763', 'Anal canal squamous carcinoma', 'XPO:0101306', 'abnormal ileum', 0.42857142857142855, 8.518562886125473, 1.9107099898944229, 'UPHENO:0076783', 'abnormal intestine morphology'),
(405134, 'HP:0001552', 'Barrel-shaped chest', 'XPO:0100584', 'abnormal vertebral column', 0.4339622641509434, 6.272837960958401, 1.6499015013598524, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(405135, 'HP:0001552', 'Barrel-shaped chest', 'XPO:0130060', 'increased size of the postcranial axial skeleton', 0.43333333333333335, 6.272837960958401, 1.6487054870661326, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(405136, 'HP:0001552', 'Barrel-shaped chest', 'XPO:0129786', 'increased size of the articular system', 0.42592592592592593, 5.972749669260594, 1.5949761544310266, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(405137, 'HP:0001552', 'Barrel-shaped chest', 'XPO:0102217', 'abnormal elastica externa morphology', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(405138, 'HP:0001552', 'Barrel-shaped chest', 'XPO:0129832', 'increased size of the skeletal system', 0.4339622641509434, 5.972749669260594, 1.6099527849223174, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(405139, 'HP:0001552', 'Barrel-shaped chest', 'XPO:0129664', 'increased size of the skeleton', 0.41818181818181815, 5.972749669260594, 1.580409857042232, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(405140, 'HP:0001552', 'Barrel-shaped chest', 'XPO:0141713', 'increased size of the posterior notochord', 0.41818181818181815, 5.972749669260594, 1.580409857042232, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(405141, 'HP:0001552', 'Barrel-shaped chest', 'XPO:0102461', 'abnormal postcranial axial skeleton morphology', 0.41818181818181815, 6.272837960958401, 1.6196255072310737, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(405142, 'HP:0001552', 'Barrel-shaped chest', 'XPO:0129726', 'increased size of the axial skeleton', 0.4067796610169492, 6.211345574613551, 1.5895436600799702, 'UPHENO:0087089', 'abnormal axial skeleton plus cranial skeleton morphology'),
(405143, 'HP:0001552', 'Barrel-shaped chest', 'XPO:0129612', 'increased size of the perichondrium', 0.40350877192982454, 5.972749669260594, 1.5524357906488784, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(405144, 'HP:0001552', 'Barrel-shaped chest', 'XPO:0103737', 'increased size of the notochord', 0.4107142857142857, 5.972749669260594, 1.5662354912849477, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(405145, 'HP:0001552', 'Barrel-shaped chest', 'XPO:0129707', 'increased size of the vertebral column', 0.40625, 6.272837960958401, 1.5963522235519798, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(405146, 'HP:0001552', 'Barrel-shaped chest', 'XPO:0102097', 'abnormal skeletal system morphology', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(405147, 'HP:0001552', 'Barrel-shaped chest', 'XPO:0141709', 'increased size of the anterior notochord', 0.41818181818181815, 5.972749669260594, 1.580409857042232, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(405148, 'HP:0001552', 'Barrel-shaped chest', 'XPO:0130908', 'increased size of the notochordal sheath', 0.41818181818181815, 5.972749669260594, 1.580409857042232, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(405149, 'HP:0001552', 'Barrel-shaped chest', 'XPO:0130368', 'increased size of the elastica externa', 0.4339622641509434, 5.972749669260594, 1.6099527849223174, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(405150, 'HP:0001552', 'Barrel-shaped chest', 'XPO:0130188', 'increased size of the flexural organ', 0.41818181818181815, 5.972749669260594, 1.580409857042232, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(405151, 'HP:0001552', 'Barrel-shaped chest', 'XPO:0129638', 'increased size of the skeletal subdivision', 0.4107142857142857, 5.972749669260594, 1.5662354912849477, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(405152, 'HP:0012627', 'Pseudoexfoliation', 'XPO:0127230', 'abnormally localised hyaloid blood vessel', 0.47692307692307695, 6.887869297006056, 1.8124524320853552, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(405153, 'HP:0012627', 'Pseudoexfoliation', 'XPO:0103110', 'abnormal lens fiber cell mass morphology', 0.44155844155844154, 9.014833150514745, 1.9951380094746995, 'UPHENO:0021038', 'abnormal anterior segment of eyeball morphology'),
(405154, 'HP:0012627', 'Pseudoexfoliation', 'XPO:0140218', 'abnormally necrotic sclera', 0.44285714285714284, 6.887869297006056, 1.7465228647932265, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(405155, 'HP:0012627', 'Pseudoexfoliation', 'XPO:0140799', 'abnormally necrotic ciliary body', 0.4155844155844156, 8.412768222102876, 1.869816933560547, 'UPHENO:0087597', 'abnormal anterior segment of eyeball morphology'),
(405156, 'HP:0012627', 'Pseudoexfoliation', 'XPO:0101359', 'abnormal hyaloid artery', 0.4305555555555556, 6.887869297006056, 1.7220947685207388, 'HP:0012372', 'Abnormal eye morphology'),
(405157, 'HP:0012627', 'Pseudoexfoliation', 'XPO:0142059', 'abnormal nasal region morphology', 0.44680851063829785, 4.5318002188002176, 1.422971154406314, 'UPHENO:0087907', 'abnormal head morphology'),
(405158, 'HP:0012627', 'Pseudoexfoliation', 'XPO:0102805', 'abnormal retinal layer morphology', 0.4492753623188406, 6.887869297006056, 1.759133301946505, 'HP:0012372', 'Abnormal eye morphology'),
(405159, 'HP:0012627', 'Pseudoexfoliation', 'XPO:0129175', 'decreased size of the lens epithelium', 0.40476190476190477, 9.014833150514745, 1.910199213986099, 'UPHENO:0021038', 'abnormal anterior segment of eyeball morphology'),
(405160, 'HP:0012627', 'Pseudoexfoliation', 'XPO:0126122', 'absent hyaloid vascular plexus', 0.4246575342465753, 6.887869297006056, 1.7102589253909142, 'HP:0012372', 'Abnormal eye morphology'),
(405161, 'HP:0012627', 'Pseudoexfoliation', 'XPO:0139722', 'abnormally necrotic hyaloid blood vessel', 0.41333333333333333, 6.887869297006056, 1.6873013886368484, 'HP:0012372', 'Abnormal eye morphology'),
(405162, 'HP:0012627', 'Pseudoexfoliation', 'XPO:0133371', 'eye fused with olfactory pit', 0.4626865671641791, 6.887869297006056, 1.7851959556606887, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(405163, 'HP:0012627', 'Pseudoexfoliation', 'XPO:0102966', 'abnormal olfactory pit morphology', 0.42105263157894735, 5.788671267106304, 1.561196743002159, 'UPHENO:0087472', 'abnormal face morphology'),
(405164, 'HP:0012627', 'Pseudoexfoliation', 'XPO:0103160', 'abnormal choroid morphology', 0.4153846153846154, 6.575878401988876, 1.652730686114997, 'UPHENO:0087924', 'abnormal camera-type eye morphology'),
(405165, 'HP:0012627', 'Pseudoexfoliation', 'XPO:0103376', 'increased size of the eye', 0.41333333333333333, 6.887869297006056, 1.6873013886368484, 'HP:0012372', 'Abnormal eye morphology'),
(405166, 'HP:0012627', 'Pseudoexfoliation', 'XPO:0102804', 'abnormal pharyngeal pouch morphology', 0.42857142857142855, 4.5318002188002176, 1.3936283915633758, 'UPHENO:0087907', 'abnormal head morphology'),
(405167, 'HP:0012627', 'Pseudoexfoliation', 'XPO:0129260', 'decreased size of the cornea', 0.41975308641975306, 9.014833150514745, 1.9452516645636548, 'UPHENO:0021038', 'abnormal anterior segment of eyeball morphology'),
(405168, 'HP:0012627', 'Pseudoexfoliation', 'XPO:0141323', 'edematous eye', 0.4696969696969697, 6.887869297006056, 1.7986693238259617, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(405169, 'HP:0012627', 'Pseudoexfoliation', 'XPO:0103022', 'abnormal ciliary body morphology', 0.4507042253521127, 8.412768222102876, 1.9472211442488363, 'UPHENO:0087597', 'abnormal anterior segment of eyeball morphology'),
(405170, 'HP:0012627', 'Pseudoexfoliation', 'XPO:0129419', 'decreased size of the pupil', 0.44155844155844154, 9.014833150514745, 1.9951380094746995, 'UPHENO:0021038', 'abnormal anterior segment of eyeball morphology'),
(405171, 'HP:0012627', 'Pseudoexfoliation', 'XPO:0102513', 'abnormal sclera morphology', 0.47692307692307695, 6.887869297006056, 1.8124524320853552, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(405172, 'HP:0012627', 'Pseudoexfoliation', 'XPO:0103336', 'decreased size of the eye', 0.41333333333333333, 6.887869297006056, 1.6873013886368484, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(405173, 'HP:0012627', 'Pseudoexfoliation', 'XPO:0102572', 'abnormal hatching gland primordium morphology', 0.4117647058823529, 4.5318002188002176, 1.3660290568695288, 'UPHENO:0087907', 'abnormal head morphology'),
(405174, 'HP:0012627', 'Pseudoexfoliation', 'XPO:0102784', 'abnormal retinal progenitor cell region morphology', 0.41333333333333333, 6.887869297006056, 1.6873013886368484, 'HP:0012372', 'Abnormal eye morphology'),
(405175, 'HP:0012627', 'Pseudoexfoliation', 'XPO:0133354', 'fused eyes', 0.4626865671641791, 6.887869297006056, 1.7851959556606887, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(405176, 'HP:0012627', 'Pseudoexfoliation', 'XPO:0126243', 'absent optic choroid vascular plexus', 0.4246575342465753, 6.887869297006056, 1.7102589253909142, 'HP:0012372', 'Abnormal eye morphology'),
(405177, 'HP:0012627', 'Pseudoexfoliation', 'XPO:0103707', 'increased pigmentation in the head', 0.42857142857142855, 4.5318002188002176, 1.3936283915633758, 'UPHENO:0087907', 'abnormal head morphology'),
(405178, 'HP:0012627', 'Pseudoexfoliation', 'XPO:0141141', 'abnormally necrotic cornea', 0.4533333333333333, 9.014833150514745, 2.021564829919309, 'UPHENO:0021038', 'abnormal anterior segment of eyeball morphology'),
(405179, 'HP:0012627', 'Pseudoexfoliation', 'XPO:0102342', 'abnormal hyaloid vein morphology', 0.4025974025974026, 6.887869297006056, 1.6652442128423794, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(405180, 'HP:0012627', 'Pseudoexfoliation', 'XPO:0128568', 'decreased size of the optic disc', 0.4090909090909091, 6.575878401988876, 1.640162209521029, 'UPHENO:0087924', 'abnormal camera-type eye morphology'),
(405181, 'HP:0012627', 'Pseudoexfoliation', 'XPO:0128643', 'decreased size of the retinal layer', 0.40789473684210525, 6.887869297006056, 1.6761639640277146, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(405182, 'HP:0012627', 'Pseudoexfoliation', 'XPO:0130893', 'increased size of the pupil', 0.4473684210526316, 9.014833150514745, 2.0082210218496126, 'UPHENO:0021038', 'abnormal anterior segment of eyeball morphology'),
(405183, 'HP:0012627', 'Pseudoexfoliation', 'XPO:0139731', 'abnormally necrotic eye', 0.43661971830985913, 6.887869297006056, 1.734179792355427, 'HP:0012372', 'Abnormal eye morphology'),
(405184, 'HP:0012627', 'Pseudoexfoliation', 'XPO:0141339', 'decreased pigmentation in the head', 0.42857142857142855, 4.5318002188002176, 1.3936283915633758, 'UPHENO:0087907', 'abnormal head morphology'),
(405185, 'HP:0012627', 'Pseudoexfoliation', 'XPO:0102212', 'abnormal globe morphology', 0.42857142857142855, 6.575878401988876, 1.6787595422967447, 'UPHENO:0087924', 'abnormal camera-type eye morphology'),
(405186, 'HP:0012627', 'Pseudoexfoliation', 'XPO:0129062', 'decreased size of the ciliary body', 0.4050632911392405, 8.412768222102876, 1.8459966369515974, 'UPHENO:0087597', 'abnormal anterior segment of eyeball morphology'),
(405187, 'HP:0012627', 'Pseudoexfoliation', 'XPO:0140452', 'abnormally necrotic lens epithelium', 0.4146341463414634, 9.014833150514745, 1.9333539892565992, 'UPHENO:0021038', 'abnormal anterior segment of eyeball morphology'),
(405188, 'HP:0012627', 'Pseudoexfoliation', 'XPO:0115526', 'abnormally incomplete structure of head', 0.44680851063829785, 4.5318002188002176, 1.422971154406314, 'UPHENO:0087907', 'abnormal head morphology'),
(405189, 'HP:0012627', 'Pseudoexfoliation', 'XPO:0102082', 'abnormal circumpharyngeal ridge morphology', 0.42, 4.5318002188002176, 1.3796217205799897, 'UPHENO:0087907', 'abnormal head morphology'),
(405190, 'HP:0012627', 'Pseudoexfoliation', 'XPO:0102003', 'abnormal hyaloid blood vessel morphology', 0.4492753623188406, 6.887869297006056, 1.759133301946505, 'HP:0012372', 'Abnormal eye morphology'),
(405191, 'HP:0012627', 'Pseudoexfoliation', 'XPO:0102862', 'abnormal iris morphology', 0.4788732394366197, 9.014833150514745, 2.077730096467687, 'UPHENO:0021038', 'abnormal anterior segment of eyeball morphology'),
(405192, 'HP:0012627', 'Pseudoexfoliation', 'XPO:0141343', 'decreased pigmentation in the eye', 0.4626865671641791, 6.887869297006056, 1.7851959556606887, 'HP:0012372', 'Abnormal eye morphology'),
(405193, 'HP:0012627', 'Pseudoexfoliation', 'XPO:0133372', 'eye fused with olfactory epithelium', 0.4626865671641791, 6.887869297006056, 1.7851959556606887, 'HP:0012372', 'Abnormal eye morphology'),
(405194, 'HP:0012627', 'Pseudoexfoliation', 'XPO:0140250', 'abnormally necrotic iris', 0.4473684210526316, 9.014833150514745, 2.0082210218496126, 'UPHENO:0021038', 'abnormal anterior segment of eyeball morphology'),
(405195, 'HP:0012627', 'Pseudoexfoliation', 'XPO:0127907', 'abnormally localised optic choroid vascular plexus', 0.45588235294117646, 6.887869297006056, 1.7720208976957377, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(405196, 'HP:0012627', 'Pseudoexfoliation', 'XPO:0103048', 'abnormal cornea morphology', 0.4927536231884058, 9.014833150514745, 2.1076270299450734, 'UPHENO:0021038', 'abnormal anterior segment of eyeball morphology'),
(405197, 'HP:0012627', 'Pseudoexfoliation', 'XPO:0102259', 'abnormal pharyngeal region morphology', 0.4666666666666667, 4.5318002188002176, 1.4542489821577214, 'UPHENO:0087907', 'abnormal head morphology'),
(405198, 'HP:0012627', 'Pseudoexfoliation', 'XPO:0140487', 'abnormally necrotic retinal layer', 0.41333333333333333, 6.887869297006056, 1.6873013886368484, 'HP:0012372', 'Abnormal eye morphology'),
(405199, 'HP:0012627', 'Pseudoexfoliation', 'XPO:0130651', 'increased size of the lens epithelium', 0.40476190476190477, 9.014833150514745, 1.910199213986099, 'UPHENO:0021038', 'abnormal anterior segment of eyeball morphology'),
(405200, 'HP:0012627', 'Pseudoexfoliation', 'XPO:0127645', 'abnormally localised hyaloid vein', 0.4492753623188406, 6.887869297006056, 1.759133301946505, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(405201, 'HP:0012627', 'Pseudoexfoliation', 'XPO:0125990', 'absent hyaloid vein', 0.4305555555555556, 6.887869297006056, 1.7220947685207388, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(405202, 'HP:0012627', 'Pseudoexfoliation', 'XPO:0141839', 'edematous pharyngeal region', 0.44680851063829785, 4.5318002188002176, 1.422971154406314, 'UPHENO:0087907', 'abnormal head morphology'),
(405203, 'HP:0012627', 'Pseudoexfoliation', 'XPO:0130736', 'increased size of the cornea', 0.41975308641975306, 9.014833150514745, 1.9452516645636548, 'UPHENO:0021038', 'abnormal anterior segment of eyeball morphology'),
(405204, 'HP:0012627', 'Pseudoexfoliation', 'XPO:0140391', 'abnormally necrotic central retina', 0.4189189189189189, 6.887869297006056, 1.6986638159319787, 'HP:0012372', 'Abnormal eye morphology'),
(405205, 'HP:0012627', 'Pseudoexfoliation', 'XPO:0128052', 'decreased size of the iris', 0.4358974358974359, 9.014833150514745, 1.982307406875276, 'UPHENO:0021038', 'abnormal anterior segment of eyeball morphology'),
(405206, 'HP:0012627', 'Pseudoexfoliation', 'XPO:0102538', 'abnormal lateral nasal prominence morphology', 0.42857142857142855, 4.5318002188002176, 1.3936283915633758, 'UPHENO:0087907', 'abnormal head morphology'),
(405207, 'HP:0012627', 'Pseudoexfoliation', 'XPO:0140192', 'abnormally necrotic retina', 0.40789473684210525, 6.887869297006056, 1.6761639640277146, 'HP:0012372', 'Abnormal eye morphology'),
(405208, 'HP:0012627', 'Pseudoexfoliation', 'XPO:0130863', 'increased size of the sclera', 0.4305555555555556, 6.887869297006056, 1.7220947685207388, 'HP:0012372', 'Abnormal eye morphology'),
(405209, 'HP:0012627', 'Pseudoexfoliation', 'XPO:0141337', 'increased pigmentation in the eye', 0.4626865671641791, 6.887869297006056, 1.7851959556606887, 'HP:0012372', 'Abnormal eye morphology'),
(405210, 'HP:0012627', 'Pseudoexfoliation', 'XPO:0100329', 'abnormal retinal blood vessel', 0.44285714285714284, 6.887869297006056, 1.7465228647932265, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(405211, 'HP:0012627', 'Pseudoexfoliation', 'XPO:0103210', 'abnormal pupil morphology', 0.4788732394366197, 9.014833150514745, 2.077730096467687, 'UPHENO:0021038', 'abnormal anterior segment of eyeball morphology'),
(405212, 'HP:0012627', 'Pseudoexfoliation', 'XPO:0103101', 'abnormal medial nasal prominence morphology', 0.42857142857142855, 4.5318002188002176, 1.3936283915633758, 'UPHENO:0087907', 'abnormal head morphology'),
(405213, 'HP:0012627', 'Pseudoexfoliation', 'XPO:0100710', 'abnormal hyaloid vein', 0.5344827586206896, 6.887869297006056, 1.9187098224803423, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(405214, 'HP:0012627', 'Pseudoexfoliation', 'XPO:0128467', 'decreased size of the lens', 0.4657534246575342, 9.014833150514745, 2.0490703776514145, 'UPHENO:0021038', 'abnormal anterior segment of eyeball morphology'),
(405215, 'HP:0012627', 'Pseudoexfoliation', 'XPO:0103739', 'increased size of the pharyngeal region', 0.42, 4.5318002188002176, 1.3796217205799897, 'UPHENO:0087907', 'abnormal head morphology'),
(405216, 'HP:0012627', 'Pseudoexfoliation', 'XPO:0103186', 'abnormal peripheral retina morphology', 0.4189189189189189, 6.887869297006056, 1.6986638159319787, 'HP:0012372', 'Abnormal eye morphology'),
(405217, 'HP:0012627', 'Pseudoexfoliation', 'XPO:0141298', 'abnormal intercanthal region morphology', 0.4375, 4.5318002188002176, 1.4080705222839853, 'UPHENO:0087907', 'abnormal head morphology'),
(405218, 'HP:0012627', 'Pseudoexfoliation', 'XPO:0125589', 'absent hyaloid blood vessel', 0.45588235294117646, 6.887869297006056, 1.7720208976957377, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(405219, 'HP:0012627', 'Pseudoexfoliation', 'XPO:0102734', 'abnormal craniofacial region morphology', 0.42857142857142855, 4.5318002188002176, 1.3936283915633758, 'UPHENO:0087907', 'abnormal head morphology'),
(405220, 'HP:0012627', 'Pseudoexfoliation', 'XPO:0129388', 'decreased size of the sclera', 0.4305555555555556, 6.887869297006056, 1.7220947685207388, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(405221, 'HP:0012627', 'Pseudoexfoliation', 'XPO:0102550', 'abnormal lens morphology', 0.5230769230769231, 9.014833150514745, 2.1715089653103203, 'UPHENO:0021038', 'abnormal anterior segment of eyeball morphology'),
(405222, 'HP:0012627', 'Pseudoexfoliation', 'XPO:0102947', 'abnormal hyaloid vascular plexus morphology', 0.40789473684210525, 6.887869297006056, 1.6761639640277146, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(405223, 'HP:0012627', 'Pseudoexfoliation', 'XPO:0130044', 'increased size of the hyaloid blood vessel', 0.4025974025974026, 6.887869297006056, 1.6652442128423794, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(405224, 'HP:0012627', 'Pseudoexfoliation', 'XPO:0101173', 'abnormal retinal layer', 0.4117647058823529, 6.02624522851634, 1.5752444553449358, 'HP:0000478', 'Abnormality of the eye'),
(405225, 'HP:0012627', 'Pseudoexfoliation', 'XPO:0102476', 'abnormal lens transitional zone morphology', 0.5074626865671642, 9.014833150514745, 2.138852834936276, 'UPHENO:0021038', 'abnormal anterior segment of eyeball morphology'),
(405226, 'HP:0012627', 'Pseudoexfoliation', 'XPO:0140223', 'abnormally necrotic head region', 0.4117647058823529, 4.5318002188002176, 1.3660290568695288, 'UPHENO:0087907', 'abnormal head morphology'),
(405227, 'HP:0012627', 'Pseudoexfoliation', 'XPO:0140538', 'abnormally necrotic optic disc', 0.421875, 6.575878401988876, 1.6655925974976766, 'UPHENO:0087924', 'abnormal camera-type eye morphology'),
(405228, 'HP:0012627', 'Pseudoexfoliation', 'XPO:0129532', 'increased size of the iris', 0.4358974358974359, 9.014833150514745, 1.982307406875276, 'UPHENO:0021038', 'abnormal anterior segment of eyeball morphology'),
(405229, 'HP:0012627', 'Pseudoexfoliation', 'XPO:0101315', 'abnormal hyaloid vascular plexus', 0.5344827586206896, 6.887869297006056, 1.9187098224803423, 'HP:0012372', 'Abnormal eye morphology'),
(405230, 'HP:0012627', 'Pseudoexfoliation', 'XPO:0128564', 'decreased size of the hyaloid blood vessel', 0.4025974025974026, 6.887869297006056, 1.6652442128423794, 'HP:0012372', 'Abnormal eye morphology'),
(405231, 'HP:0012627', 'Pseudoexfoliation', 'XPO:0101483', 'abnormal nostril', 0.46153846153846156, 5.788671267106304, 1.6345318690598054, 'UPHENO:0087472', 'abnormal face morphology'),
(405232, 'HP:0012627', 'Pseudoexfoliation', 'XPO:0130539', 'increased size of the ciliary body', 0.4050632911392405, 8.412768222102876, 1.8459966369515974, 'UPHENO:0087597', 'abnormal anterior segment of eyeball morphology'),
(405233, 'HP:0012627', 'Pseudoexfoliation', 'XPO:0130285', 'increased size of the lens transitional zone', 0.4594594594594595, 9.014833150514745, 2.0351782149120803, 'UPHENO:0021038', 'abnormal anterior segment of eyeball morphology'),
(405234, 'HP:0012627', 'Pseudoexfoliation', 'XPO:0102196', 'abnormal central retina morphology', 0.43661971830985913, 6.887869297006056, 1.734179792355427, 'HP:0012372', 'Abnormal eye morphology'),
(405235, 'HP:0012627', 'Pseudoexfoliation', 'XPO:0128935', 'decreased size of the central retina', 0.40789473684210525, 6.887869297006056, 1.6761639640277146, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(405236, 'HP:0012627', 'Pseudoexfoliation', 'XPO:0127783', 'abnormally localised hyaloid vascular plexus', 0.44285714285714284, 6.887869297006056, 1.7465228647932265, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(405237, 'HP:0012627', 'Pseudoexfoliation', 'XPO:0115423', 'abnormally incomplete structure of eye', 0.47692307692307695, 6.887869297006056, 1.8124524320853552, 'HP:0012372', 'Abnormal eye morphology'),
(405238, 'HP:0012627', 'Pseudoexfoliation', 'XPO:0103358', 'decreased size of the pharyngeal region', 0.42, 4.5318002188002176, 1.3796217205799897, 'UPHENO:0087907', 'abnormal head morphology'),
(405239, 'HP:0012627', 'Pseudoexfoliation', 'XPO:0102226', 'abnormal Jacobsons organ morphology', 0.4067796610169492, 5.788671267106304, 1.5345076525622334, 'UPHENO:0087472', 'abnormal face morphology'),
(405240, 'HP:0012627', 'Pseudoexfoliation', 'XPO:0140335', 'abnormally necrotic pharyngeal region', 0.4375, 4.5318002188002176, 1.4080705222839853, 'UPHENO:0087907', 'abnormal head morphology'),
(405241, 'HP:0012627', 'Pseudoexfoliation', 'XPO:0130413', 'increased size of the central retina', 0.40789473684210525, 6.887869297006056, 1.6761639640277146, 'HP:0012372', 'Abnormal eye morphology'),
(405242, 'HP:0012627', 'Pseudoexfoliation', 'XPO:0100779', 'abnormal optic choroid vascular plexus', 0.543859649122807, 6.887869297006056, 1.9354674316747025, 'HP:0012372', 'Abnormal eye morphology'),
(405243, 'HP:0012627', 'Pseudoexfoliation', 'XPO:0102117', 'abnormal retina morphology', 0.43661971830985913, 6.887869297006056, 1.734179792355427, 'HP:0012372', 'Abnormal eye morphology'),
(405244, 'HP:0012627', 'Pseudoexfoliation', 'XPO:0101823', 'abnormal lens epithelium morphology', 0.4594594594594595, 9.014833150514745, 2.0351782149120803, 'UPHENO:0021038', 'abnormal anterior segment of eyeball morphology'),
(405245, 'HP:0012627', 'Pseudoexfoliation', 'XPO:0141638', 'neoplastic eye', 0.4626865671641791, 6.887869297006056, 1.7851959556606887, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(405246, 'HP:0012627', 'Pseudoexfoliation', 'XPO:0101817', 'abnormal eye morphology', 0.484375, 6.887869297006056, 1.8265573330003382, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(405247, 'HP:0012627', 'Pseudoexfoliation', 'XPO:0100420', 'abnormal choana', 0.4444444444444444, 5.788671267106304, 1.6039771773253444, 'UPHENO:0087472', 'abnormal face morphology'),
(405248, 'HP:0012627', 'Pseudoexfoliation', 'XPO:0129947', 'increased size of the lens', 0.4657534246575342, 9.014833150514745, 2.0490703776514145, 'UPHENO:0021038', 'abnormal anterior segment of eyeball morphology'),
(405249, 'HP:0012627', 'Pseudoexfoliation', 'XPO:0140473', 'abnormally necrotic lens transitional zone', 0.4722222222222222, 9.014833150514745, 2.0632509646910697, 'UPHENO:0021038', 'abnormal anterior segment of eyeball morphology'),
(405250, 'HP:0012627', 'Pseudoexfoliation', 'XPO:0141835', 'edematous head', 0.4375, 4.5318002188002176, 1.4080705222839853, 'UPHENO:0087907', 'abnormal head morphology'),
(405251, 'HP:0012627', 'Pseudoexfoliation', 'XPO:0140375', 'abnormally necrotic lens', 0.4857142857142857, 9.014833150514745, 2.0925183976576487, 'UPHENO:0021038', 'abnormal anterior segment of eyeball morphology'),
(405252, 'HP:0012627', 'Pseudoexfoliation', 'XPO:0102505', 'abnormal retinal stem cell region morphology', 0.41333333333333333, 6.887869297006056, 1.6873013886368484, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(405253, 'HP:0012627', 'Pseudoexfoliation', 'XPO:0130122', 'increased size of the retinal layer', 0.40789473684210525, 6.887869297006056, 1.6761639640277146, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(405254, 'HP:0012627', 'Pseudoexfoliation', 'XPO:0139715', 'abnormally necrotic head', 0.4117647058823529, 4.5318002188002176, 1.3660290568695288, 'UPHENO:0087907', 'abnormal head morphology'),
(405255, 'HP:0012627', 'Pseudoexfoliation', 'XPO:0102831', 'abnormal optic disc morphology', 0.4426229508196721, 6.575878401988876, 1.7060582353834428, 'UPHENO:0087924', 'abnormal camera-type eye morphology'),
(405256, 'HP:0012627', 'Pseudoexfoliation', 'XPO:0133369', 'eye fused with brain', 0.4626865671641791, 6.887869297006056, 1.7851959556606887, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(405257, 'HP:0012627', 'Pseudoexfoliation', 'XPO:0115417', 'abnormally wholly ventralized eye', 0.43661971830985913, 6.887869297006056, 1.734179792355427, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(405258, 'HP:0012627', 'Pseudoexfoliation', 'XPO:0130048', 'increased size of the optic disc', 0.4090909090909091, 6.575878401988876, 1.640162209521029, 'UPHENO:0087924', 'abnormal camera-type eye morphology'),
(405259, 'HP:0012627', 'Pseudoexfoliation', 'XPO:0101634', 'abnormal head morphology', 0.45652173913043476, 4.5318002188002176, 1.4383550734357495, 'UPHENO:0087907', 'abnormal head morphology'),
(405260, 'HP:0012627', 'Pseudoexfoliation', 'XPO:0100371', 'abnormal hyaloid blood vessel', 0.5535714285714286, 6.887869297006056, 1.9526719249676645, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(405261, 'HP:0012627', 'Pseudoexfoliation', 'XPO:0128807', 'decreased size of the lens transitional zone', 0.4594594594594595, 9.014833150514745, 2.0351782149120803, 'UPHENO:0021038', 'abnormal anterior segment of eyeball morphology'),
(405262, 'HP:0012627', 'Pseudoexfoliation', 'XPO:0140914', 'abnormally necrotic intercanthal region', 0.4117647058823529, 4.5318002188002176, 1.3660290568695288, 'UPHENO:0087907', 'abnormal head morphology'),
(405263, 'HP:0001693', 'Cardiac shunt', 'XPO:0141841', 'abnormality of whole organism mass', 0.41935483870967744, 3.334430194052109, 1.1825013472361883, 'UPHENO:0049587', 'abnormal biological_process'),
(405264, 'HP:0001693', 'Cardiac shunt', 'XPO:0141776', 'abnormal metabolic process', 0.4074074074074074, 3.334430194052109, 1.1655348817344542, 'UPHENO:0049587', 'abnormal biological_process'),
(405265, 'HP:0001693', 'Cardiac shunt', 'XPO:0100054', 'abnormal blood vessel', 0.4117647058823529, 5.249153838287537, 1.4701755971154233, 'UPHENO:0080362', 'abnormal cardiovascular system'),
(405266, 'HP:0025410', 'Splenogonadal fusion', 'XPO:0102078', 'abnormal spleen morphology', 0.5342465753424658, 11.212049843624797, 2.44744749310901, 'UPHENO:0076790', 'abnormal spleen morphology'),
(405267, 'HP:0025410', 'Splenogonadal fusion', 'XPO:0140119', 'abnormally necrotic spleen', 0.47560975609756095, 11.212049843624797, 2.309233702222468, 'UPHENO:0076790', 'abnormal spleen morphology'),
(405268, 'HP:0025410', 'Splenogonadal fusion', 'XPO:0100446', 'abnormal spleen', 0.4461538461538462, 10.484129389061598, 2.1627608861139516, 'HP:0001743', 'Abnormality of the spleen'),
(405269, 'HP:0025410', 'Splenogonadal fusion', 'XPO:0130675', 'increased size of the spleen', 0.42391304347826086, 11.212049843624797, 2.1801225132640933, 'UPHENO:0076790', 'abnormal spleen morphology'),
(405270, 'HP:0025410', 'Splenogonadal fusion', 'XPO:0125198', 'absent spleen', 0.44047619047619047, 11.212049843624797, 2.222305335130395, 'UPHENO:0076790', 'abnormal spleen morphology'),
(405271, 'HP:0025410', 'Splenogonadal fusion', 'XPO:0129199', 'decreased size of the spleen', 0.45348837209302323, 11.212049843624797, 2.254891179505398, 'UPHENO:0076790', 'abnormal spleen morphology'),
(405272, 'HP:0025410', 'Splenogonadal fusion', 'XPO:0141656', 'neoplastic spleen', 0.52, 11.212049843624797, 2.4145943590352594, 'UPHENO:0076790', 'abnormal spleen morphology'),
(405273, 'HP:0025410', 'Splenogonadal fusion', 'XPO:0141626', 'metaplastic spleen', 0.43283582089552236, 10.484129389061598, 2.1302363132970363, 'HP:0001743', 'Abnormality of the spleen'),
(405274, 'HP:0009416', 'Ivory epiphyses of the 3rd finger', 'XPO:0103609', 'abnormally increased number of forelimb digit in the regenerating forelimb', 0.40714285714285714, 7.774297771301195, 1.7791148942344661, 'HP:0005918', 'Abnormal finger phalanx morphology'),
(405275, 'HP:0009416', 'Ivory epiphyses of the 3rd finger', 'XPO:0103634', 'abnormally increased number of forelimb digit', 0.4253731343283582, 7.774297771301195, 1.8185096673321148, 'HP:0005918', 'Abnormal finger phalanx morphology'),
(405276, 'HP:0000263', 'Oxycephaly', 'XPO:0141829', 'increased width of head', 0.5, 7.024697770424301, 1.8741261657669024, 'HP:0000929', 'Abnormal skull morphology'),
(405277, 'HP:0000263', 'Oxycephaly', 'XPO:0102005', 'abnormal splanchnocranium morphology', 0.48148148148148145, 4.638757693672553, 1.4944818254442178, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(405278, 'HP:0000263', 'Oxycephaly', 'XPO:0102665', 'abnormal suspensorium morphology', 0.48148148148148145, 4.638757693672553, 1.4944818254442178, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(405279, 'HP:0000263', 'Oxycephaly', 'XPO:0130449', 'increased size of the fenestra subocularis', 0.4482758620689655, 4.638757693672553, 1.4420274283314136, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(405280, 'HP:0000263', 'Oxycephaly', 'XPO:0103176', 'abnormal fenestra basicranialis morphology', 0.49056603773584906, 4.638757693672553, 1.508514826510376, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(405281, 'HP:0000263', 'Oxycephaly', 'XPO:0103739', 'increased size of the pharyngeal region', 0.42, 4.5318002188002176, 1.3796217205799897, 'UPHENO:0087907', 'abnormal head morphology'),
(405282, 'HP:0000263', 'Oxycephaly', 'XPO:0128477', 'decreased size of the neurocranium', 0.49206349206349204, 7.024697770424301, 1.8591926515575539, 'HP:0000929', 'Abnormal skull morphology'),
(405283, 'HP:0000263', 'Oxycephaly', 'XPO:0140335', 'abnormally necrotic pharyngeal region', 0.4375, 4.5318002188002176, 1.4080705222839853, 'UPHENO:0087907', 'abnormal head morphology'),
(405284, 'HP:0000263', 'Oxycephaly', 'XPO:0100420', 'abnormal choana', 0.4444444444444444, 4.5318002188002176, 1.4192016877730502, 'UPHENO:0087907', 'abnormal head morphology'),
(405285, 'HP:0000263', 'Oxycephaly', 'XPO:0102921', 'abnormal orbital region morphology', 0.5, 7.024697770424301, 1.8741261657669024, 'HP:0000929', 'Abnormal skull morphology'),
(405286, 'HP:0000263', 'Oxycephaly', 'XPO:0103138', 'abnormal upper jaw morphology', 0.43661971830985913, 7.024697770424301, 1.7513199484202062, 'HP:0000929', 'Abnormal skull morphology'),
(405287, 'HP:0000263', 'Oxycephaly', 'XPO:0102734', 'abnormal craniofacial region morphology', 0.42857142857142855, 4.5318002188002176, 1.3936283915633758, 'UPHENO:0087907', 'abnormal head morphology'),
(405288, 'HP:0000263', 'Oxycephaly', 'XPO:0129513', 'increased size of the splanchnocranium', 0.41935483870967744, 4.638757693672553, 1.394734915474381, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(405289, 'HP:0000263', 'Oxycephaly', 'XPO:0101634', 'abnormal head morphology', 0.45652173913043476, 4.5318002188002176, 1.4383550734357495, 'UPHENO:0087907', 'abnormal head morphology'),
(405290, 'HP:0000263', 'Oxycephaly', 'XPO:0128880', 'decreased size of the lower jaw', 0.40789473684210525, 7.024697770424301, 1.6927307076031153, 'HP:0000929', 'Abnormal skull morphology'),
(405291, 'HP:0000263', 'Oxycephaly', 'XPO:0128291', 'decreased size of the dermatocranium', 0.41935483870967744, 4.638757693672553, 1.394734915474381, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(405292, 'HP:0000263', 'Oxycephaly', 'XPO:0129957', 'increased size of the neurocranium', 0.49206349206349204, 7.024697770424301, 1.8591926515575539, 'HP:0000929', 'Abnormal skull morphology'),
(405293, 'HP:0000263', 'Oxycephaly', 'XPO:0102828', 'abnormal occipital region morphology', 0.5740740740740741, 7.024697770424301, 2.008157580521644, 'HP:0000929', 'Abnormal skull morphology'),
(405294, 'HP:0000263', 'Oxycephaly', 'XPO:0130880', 'increased size of the suspensorium', 0.4262295081967213, 4.638757693672553, 1.4061206955371255, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(405295, 'HP:0000263', 'Oxycephaly', 'XPO:0142059', 'abnormal nasal region morphology', 0.44680851063829785, 4.5318002188002176, 1.422971154406314, 'UPHENO:0087907', 'abnormal head morphology'),
(405296, 'HP:0000263', 'Oxycephaly', 'XPO:0128034', 'decreased size of the cranium', 0.4406779661016949, 4.638757693672553, 1.4297546312868548, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(405297, 'HP:0000263', 'Oxycephaly', 'XPO:0102806', 'abnormal articular system morphology', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(405298, 'HP:0000263', 'Oxycephaly', 'XPO:0130324', 'increased size of the choana', 0.4696969696969697, 7.024697770424301, 1.8164468766813286, 'HP:0000929', 'Abnormal skull morphology'),
(405299, 'HP:0000263', 'Oxycephaly', 'XPO:0128846', 'decreased size of the choana', 0.4696969696969697, 7.024697770424301, 1.8164468766813286, 'HP:0000929', 'Abnormal skull morphology'),
(405300, 'HP:0000263', 'Oxycephaly', 'XPO:0102097', 'abnormal skeletal system morphology', 0.43478260869565216, 4.638757693672553, 1.4201588541997616, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(405301, 'HP:0000263', 'Oxycephaly', 'XPO:0101681', 'abnormal chondrocranium morphology', 0.48148148148148145, 4.638757693672553, 1.4944818254442178, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(405302, 'HP:0000263', 'Oxycephaly', 'XPO:0129291', 'decreased size of the orbital region', 0.43661971830985913, 7.024697770424301, 1.7513199484202062, 'HP:0000929', 'Abnormal skull morphology'),
(405303, 'HP:0000263', 'Oxycephaly', 'XPO:0102804', 'abnormal pharyngeal pouch morphology', 0.42857142857142855, 4.5318002188002176, 1.3936283915633758, 'UPHENO:0087907', 'abnormal head morphology'),
(405304, 'HP:0000263', 'Oxycephaly', 'XPO:0102776', 'abnormal fenestra subocularis morphology', 0.49056603773584906, 4.638757693672553, 1.508514826510376, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(405305, 'HP:0000263', 'Oxycephaly', 'XPO:0100693', 'abnormal vertebral centrum', 0.40350877192982454, 6.272837960958401, 1.5909573036826314, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(405306, 'HP:0000263', 'Oxycephaly', 'XPO:0130767', 'increased size of the orbital region', 0.43661971830985913, 7.024697770424301, 1.7513199484202062, 'HP:0000929', 'Abnormal skull morphology'),
(405307, 'HP:0000263', 'Oxycephaly', 'XPO:0140560', 'abnormally necrotic orbital region', 0.4626865671641791, 7.024697770424301, 1.8028403414510898, 'HP:0000929', 'Abnormal skull morphology'),
(405308, 'HP:0000263', 'Oxycephaly', 'XPO:0103721', 'increased size of the chondrocranium', 0.41935483870967744, 4.638757693672553, 1.394734915474381, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(405309, 'HP:0000263', 'Oxycephaly', 'XPO:0130425', 'increased size of the otic region', 0.5, 7.024697770424301, 1.8741261657669024, 'HP:0000929', 'Abnormal skull morphology'),
(405310, 'HP:0000263', 'Oxycephaly', 'XPO:0129406', 'decreased size of the suspensorium', 0.4262295081967213, 4.638757693672553, 1.4061206955371255, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(405311, 'HP:0000263', 'Oxycephaly', 'XPO:0102720', 'abnormal dermatocranium morphology', 0.48148148148148145, 4.638757693672553, 1.4944818254442178, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(405312, 'HP:0000263', 'Oxycephaly', 'XPO:0102052', 'abnormal choana morphology', 0.5166666666666667, 7.024697770424301, 1.9051055564944135, 'HP:0000929', 'Abnormal skull morphology'),
(405313, 'HP:0000263', 'Oxycephaly', 'XPO:0141185', 'abnormally necrotic occipital region', 0.5254237288135594, 7.024697770424301, 1.9211826816637279, 'HP:0000929', 'Abnormal skull morphology'),
(405314, 'HP:0000263', 'Oxycephaly', 'XPO:0101957', 'abnormal axial skeleton morphology', 0.4117647058823529, 6.211345574613551, 1.599253852164941, 'UPHENO:0087089', 'abnormal axial skeleton plus cranial skeleton morphology'),
(405315, 'HP:0000263', 'Oxycephaly', 'XPO:0139715', 'abnormally necrotic head', 0.4117647058823529, 4.5318002188002176, 1.3660290568695288, 'UPHENO:0087907', 'abnormal head morphology'),
(405316, 'HP:0000263', 'Oxycephaly', 'XPO:0130383', 'increased size of the occipital region', 0.5081967213114754, 7.024697770424301, 1.8894254087244782, 'HP:0000929', 'Abnormal skull morphology'),
(405317, 'HP:0000263', 'Oxycephaly', 'XPO:0128659', 'decreased size of the braincase and otic capsule skeleton', 0.40625, 4.638757693672553, 1.3727692133255593, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(405318, 'HP:0000263', 'Oxycephaly', 'XPO:0128033', 'decreased size of the splanchnocranium', 0.41935483870967744, 4.638757693672553, 1.394734915474381, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(405319, 'HP:0000263', 'Oxycephaly', 'XPO:0129689', 'increased size of the sphenoid region', 0.5, 7.024697770424301, 1.8741261657669024, 'HP:0000929', 'Abnormal skull morphology'),
(405320, 'HP:0000263', 'Oxycephaly', 'XPO:0128947', 'decreased size of the otic region', 0.5, 7.024697770424301, 1.8741261657669024, 'HP:0000929', 'Abnormal skull morphology'),
(405321, 'HP:0000263', 'Oxycephaly', 'XPO:0141835', 'edematous head', 0.4375, 4.5318002188002176, 1.4080705222839853, 'UPHENO:0087907', 'abnormal head morphology'),
(405322, 'HP:0000263', 'Oxycephaly', 'XPO:0128905', 'decreased size of the occipital region', 0.5081967213114754, 7.024697770424301, 1.8894254087244782, 'HP:0000929', 'Abnormal skull morphology'),
(405323, 'HP:0000263', 'Oxycephaly', 'XPO:0102538', 'abnormal lateral nasal prominence morphology', 0.42857142857142855, 4.5318002188002176, 1.3936283915633758, 'UPHENO:0087907', 'abnormal head morphology'),
(405324, 'HP:0000263', 'Oxycephaly', 'XPO:0102401', 'abnormal neurocranium morphology', 0.5636363636363636, 7.024697770424301, 1.9898178577363366, 'HP:0000929', 'Abnormal skull morphology'),
(405325, 'HP:0000263', 'Oxycephaly', 'XPO:0102082', 'abnormal circumpharyngeal ridge morphology', 0.42, 4.5318002188002176, 1.3796217205799897, 'UPHENO:0087907', 'abnormal head morphology'),
(405326, 'HP:0000263', 'Oxycephaly', 'XPO:0141193', 'abnormally necrotic mandibular arch skeleton', 0.4126984126984127, 4.638757693672553, 1.3836213127410304, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(405327, 'HP:0000263', 'Oxycephaly', 'XPO:0130147', 'increased size of the fenestra basicranialis', 0.4482758620689655, 4.638757693672553, 1.4420274283314136, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(405328, 'HP:0000263', 'Oxycephaly', 'XPO:0140639', 'abnormally necrotic upper jaw', 0.40789473684210525, 7.024697770424301, 1.6927307076031153, 'HP:0000929', 'Abnormal skull morphology'),
(405329, 'HP:0000263', 'Oxycephaly', 'XPO:0128668', 'decreased size of the fenestra basicranialis', 0.4482758620689655, 4.638757693672553, 1.4420274283314136, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(405330, 'HP:0000263', 'Oxycephaly', 'XPO:0102144', 'abnormal cranial skeleton morphology', 0.40384615384615385, 6.211345574613551, 1.5838017617482976, 'UPHENO:0087089', 'abnormal axial skeleton plus cranial skeleton morphology'),
(405331, 'HP:0000263', 'Oxycephaly', 'XPO:0102215', 'abnormal mandibular arch skeleton morphology', 0.45614035087719296, 4.638757693672553, 1.4546217934659431, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(405332, 'HP:0000263', 'Oxycephaly', 'XPO:0129688', 'increased size of the olfactory region', 0.5, 7.024697770424301, 1.8741261657669024, 'HP:0000929', 'Abnormal skull morphology'),
(405333, 'HP:0000263', 'Oxycephaly', 'XPO:0103707', 'increased pigmentation in the head', 0.42857142857142855, 4.5318002188002176, 1.3936283915633758, 'UPHENO:0087907', 'abnormal head morphology'),
(405334, 'HP:0000263', 'Oxycephaly', 'XPO:0139880', 'abnormally necrotic dermatocranium', 0.43333333333333335, 4.638757693672553, 1.4177899470389728, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(405335, 'HP:0000263', 'Oxycephaly', 'XPO:0128971', 'decreased size of the fenestra subocularis', 0.4482758620689655, 4.638757693672553, 1.4420274283314136, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(405336, 'HP:0000263', 'Oxycephaly', 'XPO:0102795', 'abnormal branchial basket morphology', 0.40625, 4.638757693672553, 1.3727692133255593, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(405337, 'HP:0000263', 'Oxycephaly', 'XPO:0128209', 'decreased size of the sphenoid region', 0.5, 7.024697770424301, 1.8741261657669024, 'HP:0000929', 'Abnormal skull morphology'),
(405338, 'HP:0000263', 'Oxycephaly', 'XPO:0102259', 'abnormal pharyngeal region morphology', 0.4666666666666667, 4.5318002188002176, 1.4542489821577214, 'UPHENO:0087907', 'abnormal head morphology'),
(405339, 'HP:0000263', 'Oxycephaly', 'XPO:0107372', 'abnormal flexural organ morphology', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(405340, 'HP:0000263', 'Oxycephaly', 'XPO:0141201', 'abnormally necrotic sphenoid region', 0.5166666666666667, 7.024697770424301, 1.9051055564944135, 'HP:0000929', 'Abnormal skull morphology'),
(405341, 'HP:0000263', 'Oxycephaly', 'XPO:0141839', 'edematous pharyngeal region', 0.44680851063829785, 4.5318002188002176, 1.422971154406314, 'UPHENO:0087907', 'abnormal head morphology'),
(405342, 'HP:0000263', 'Oxycephaly', 'XPO:0102272', 'abnormal notochordal sheath morphology', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(405343, 'HP:0000263', 'Oxycephaly', 'XPO:0139832', 'abnormally necrotic splanchnocranium', 0.43333333333333335, 4.638757693672553, 1.4177899470389728, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(405344, 'HP:0000263', 'Oxycephaly', 'XPO:0102092', 'abnormal ethmoid region morphology', 0.49056603773584906, 4.638757693672553, 1.508514826510376, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(405345, 'HP:0000263', 'Oxycephaly', 'XPO:0103101', 'abnormal medial nasal prominence morphology', 0.42857142857142855, 4.5318002188002176, 1.3936283915633758, 'UPHENO:0087907', 'abnormal head morphology'),
(405346, 'HP:0000263', 'Oxycephaly', 'XPO:0101860', 'abnormal skeletal subdivision morphology', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(405347, 'HP:0000263', 'Oxycephaly', 'XPO:0103332', 'decreased size of the chondrocranium', 0.41935483870967744, 4.638757693672553, 1.394734915474381, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(405348, 'HP:0000263', 'Oxycephaly', 'XPO:0140914', 'abnormally necrotic intercanthal region', 0.4117647058823529, 4.5318002188002176, 1.3660290568695288, 'UPHENO:0087907', 'abnormal head morphology'),
(405349, 'HP:0000263', 'Oxycephaly', 'XPO:0140897', 'abnormally necrotic lower jaw', 0.4189189189189189, 7.024697770424301, 1.7154529418548001, 'HP:0000929', 'Abnormal skull morphology'),
(405350, 'HP:0000263', 'Oxycephaly', 'XPO:0139745', 'abnormally necrotic chondrocranium', 0.43333333333333335, 4.638757693672553, 1.4177899470389728, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(405351, 'HP:0000263', 'Oxycephaly', 'XPO:0129514', 'increased size of the cranium', 0.4406779661016949, 4.638757693672553, 1.4297546312868548, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(405352, 'HP:0000263', 'Oxycephaly', 'XPO:0101997', 'abnormal braincase and otic capsule skeleton morphology', 0.4642857142857143, 4.638757693672553, 1.4675520192501232, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(405353, 'HP:0000263', 'Oxycephaly', 'XPO:0102461', 'abnormal postcranial axial skeleton morphology', 0.4423076923076923, 6.272837960958401, 1.6656903922192745, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(405354, 'HP:0000263', 'Oxycephaly', 'XPO:0140223', 'abnormally necrotic head region', 0.4117647058823529, 4.5318002188002176, 1.3660290568695288, 'UPHENO:0087907', 'abnormal head morphology'),
(405355, 'HP:0000263', 'Oxycephaly', 'XPO:0102564', 'abnormal olfactory region morphology', 0.5636363636363636, 7.024697770424301, 1.9898178577363366, 'HP:0000929', 'Abnormal skull morphology'),
(405356, 'HP:0000263', 'Oxycephaly', 'XPO:0103358', 'decreased size of the pharyngeal region', 0.42, 4.5318002188002176, 1.3796217205799897, 'UPHENO:0087907', 'abnormal head morphology'),
(405357, 'HP:0000263', 'Oxycephaly', 'XPO:0129771', 'increased size of the dermatocranium', 0.41935483870967744, 4.638757693672553, 1.394734915474381, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(405358, 'HP:0000263', 'Oxycephaly', 'XPO:0101764', 'abnormal cranium morphology', 0.5, 4.638757693672553, 1.5229507040072823, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(405359, 'HP:0000263', 'Oxycephaly', 'XPO:0102572', 'abnormal hatching gland primordium morphology', 0.4117647058823529, 4.5318002188002176, 1.3660290568695288, 'UPHENO:0087907', 'abnormal head morphology'),
(405360, 'HP:0000263', 'Oxycephaly', 'XPO:0129718', 'increased size of the ethmoid region', 0.43333333333333335, 4.638757693672553, 1.4177899470389728, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(405361, 'HP:0000263', 'Oxycephaly', 'XPO:0139775', 'abnormally necrotic braincase and otic capsule skeleton', 0.41935483870967744, 4.638757693672553, 1.394734915474381, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(405362, 'HP:0000263', 'Oxycephaly', 'XPO:0140132', 'abnormally necrotic ethmoid region', 0.4482758620689655, 4.638757693672553, 1.4420274283314136, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(405363, 'HP:0000263', 'Oxycephaly', 'XPO:0139784', 'abnormally necrotic cranium', 0.45614035087719296, 4.638757693672553, 1.4546217934659431, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(405364, 'HP:0000263', 'Oxycephaly', 'XPO:0130138', 'increased size of the braincase and otic capsule skeleton', 0.40625, 4.638757693672553, 1.3727692133255593, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(405365, 'HP:0000263', 'Oxycephaly', 'XPO:0100226', 'abnormal vertebral element', 0.4107142857142857, 6.272837960958401, 1.6050994245019483, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(405366, 'HP:0000263', 'Oxycephaly', 'XPO:0102485', 'abnormal osseous labyrinth morphology', 0.41333333333333333, 7.024697770424301, 1.7039782114536297, 'HP:0000929', 'Abnormal skull morphology'),
(405367, 'HP:0000263', 'Oxycephaly', 'XPO:0140644', 'abnormally necrotic otic region', 0.5166666666666667, 7.024697770424301, 1.9051055564944135, 'HP:0000929', 'Abnormal skull morphology'),
(405368, 'HP:0000263', 'Oxycephaly', 'XPO:0128238', 'decreased size of the ethmoid region', 0.43333333333333335, 4.638757693672553, 1.4177899470389728, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(405369, 'HP:0000263', 'Oxycephaly', 'XPO:0103381', 'increased size of the head', 0.5344827586206896, 7.024697770424301, 1.9376738226061134, 'HP:0000929', 'Abnormal skull morphology'),
(405370, 'HP:0000263', 'Oxycephaly', 'XPO:0103152', 'abnormal otic region morphology', 0.5636363636363636, 7.024697770424301, 1.9898178577363366, 'HP:0000929', 'Abnormal skull morphology'),
(405371, 'HP:0000263', 'Oxycephaly', 'XPO:0140672', 'abnormally necrotic olfactory region', 0.5166666666666667, 7.024697770424301, 1.9051055564944135, 'HP:0000929', 'Abnormal skull morphology'),
(405372, 'HP:0000263', 'Oxycephaly', 'XPO:0128208', 'decreased size of the olfactory region', 0.5, 7.024697770424301, 1.8741261657669024, 'HP:0000929', 'Abnormal skull morphology'),
(405373, 'HP:0000263', 'Oxycephaly', 'XPO:0102010', 'abnormal perichondrium morphology', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(405374, 'HP:0000263', 'Oxycephaly', 'XPO:0102216', 'abnormal vertebral column morphology', 0.4107142857142857, 6.272837960958401, 1.6050994245019483, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(405375, 'HP:0000263', 'Oxycephaly', 'XPO:0115586', 'abnormally decreased volume of chondrocranium', 0.40625, 4.638757693672553, 1.3727692133255593, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(405376, 'HP:0000263', 'Oxycephaly', 'XPO:0140926', 'abnormally necrotic neurocranium', 0.5166666666666667, 7.024697770424301, 1.9051055564944135, 'HP:0000929', 'Abnormal skull morphology'),
(405377, 'HP:0000263', 'Oxycephaly', 'XPO:0100584', 'abnormal vertebral column', 0.46, 6.272837960958401, 1.69867756270602, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(405378, 'HP:0000263', 'Oxycephaly', 'XPO:0102351', 'abnormal sphenoid region morphology', 0.5636363636363636, 7.024697770424301, 1.9898178577363366, 'HP:0000929', 'Abnormal skull morphology'),
(405379, 'HP:0000263', 'Oxycephaly', 'XPO:0141061', 'abnormally necrotic suspensorium', 0.4406779661016949, 4.638757693672553, 1.4297546312868548, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(405380, 'HP:0000263', 'Oxycephaly', 'XPO:0115526', 'abnormally incomplete structure of head', 0.44680851063829785, 4.5318002188002176, 1.422971154406314, 'UPHENO:0087907', 'abnormal head morphology'),
(405381, 'HP:0000263', 'Oxycephaly', 'XPO:0101659', 'abnormal lower jaw morphology', 0.4492753623188406, 7.024697770424301, 1.7765200916363793, 'HP:0000929', 'Abnormal skull morphology'),
(405382, 'HP:0000263', 'Oxycephaly', 'XPO:0141339', 'decreased pigmentation in the head', 0.42857142857142855, 4.5318002188002176, 1.3936283915633758, 'UPHENO:0087907', 'abnormal head morphology'),
(405383, 'HP:0000263', 'Oxycephaly', 'XPO:0141723', 'abnormal posterior notochord morphology', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(405384, 'HP:0000263', 'Oxycephaly', 'XPO:0102567', 'abnormal skeleton morphology', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(405385, 'HP:0000263', 'Oxycephaly', 'XPO:0130358', 'increased size of the lower jaw', 0.40789473684210525, 7.024697770424301, 1.6927307076031153, 'HP:0000929', 'Abnormal skull morphology'),
(405386, 'HP:0000263', 'Oxycephaly', 'XPO:0141298', 'abnormal intercanthal region morphology', 0.4375, 4.5318002188002176, 1.4080705222839853, 'UPHENO:0087907', 'abnormal head morphology'),
(405387, 'HP:0000263', 'Oxycephaly', 'XPO:0102054', 'abnormal notochord morphology', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(405388, 'HP:0000263', 'Oxycephaly', 'XPO:0141719', 'abnormal anterior notochord morphology', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(405389, 'HP:0000263', 'Oxycephaly', 'XPO:0102217', 'abnormal elastica externa morphology', 0.43478260869565216, 4.638757693672553, 1.4201588541997616, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(405390, 'HP:0033708', 'Anti-3-hydroxy- 3-methylglutaryl-coA reductase antibody positivity', 'XPO:0100745', 'abnormal anterior lymph sac', 0.43333333333333335, 5.64885357140806, 1.5645563421015427, 'HP:0002715', 'Abnormality of the immune system'),
(405391, 'HP:0033708', 'Anti-3-hydroxy- 3-methylglutaryl-coA reductase antibody positivity', 'XPO:0141497', 'abnormal lymphoblast', 0.41935483870967744, 5.64885357140806, 1.5391147060347428, 'HP:0002715', 'Abnormality of the immune system'),
(405392, 'HP:0033708', 'Anti-3-hydroxy- 3-methylglutaryl-coA reductase antibody positivity', 'XPO:0101451', 'abnormal dorsal lymph space', 0.4482758620689655, 5.64885357140806, 1.5913028324062968, 'HP:0002715', 'Abnormality of the immune system'),
(405393, 'HP:0033708', 'Anti-3-hydroxy- 3-methylglutaryl-coA reductase antibody positivity', 'XPO:0100242', 'abnormal right lymph heart', 0.40625, 5.64885357140806, 1.5148751642906173, 'HP:0002715', 'Abnormality of the immune system'),
(405394, 'HP:0033708', 'Anti-3-hydroxy- 3-methylglutaryl-coA reductase antibody positivity', 'XPO:0100599', 'abnormal adult immune system', 0.4642857142857143, 5.64885357140806, 1.6194696710023933, 'HP:0002715', 'Abnormality of the immune system'),
(405395, 'HP:0033708', 'Anti-3-hydroxy- 3-methylglutaryl-coA reductase antibody positivity', 'XPO:0100540', 'abnormal left lymph heart', 0.40625, 5.64885357140806, 1.5148751642906173, 'HP:0002715', 'Abnormality of the immune system'),
(405396, 'HP:0033708', 'Anti-3-hydroxy- 3-methylglutaryl-coA reductase antibody positivity', 'XPO:0101029', 'abnormal right spleen primordium', 0.41935483870967744, 5.64885357140806, 1.5391147060347428, 'HP:0002715', 'Abnormality of the immune system'),
(405397, 'HP:0033708', 'Anti-3-hydroxy- 3-methylglutaryl-coA reductase antibody positivity', 'XPO:0101221', 'abnormal larval immune system', 0.4642857142857143, 5.64885357140806, 1.6194696710023933, 'HP:0002715', 'Abnormality of the immune system'),
(405398, 'HP:0033708', 'Anti-3-hydroxy- 3-methylglutaryl-coA reductase antibody positivity', 'XPO:0101518', 'abnormal B cell', 0.40625, 5.64885357140806, 1.5148751642906173, 'HP:0002715', 'Abnormality of the immune system'),
(405399, 'HP:0033708', 'Anti-3-hydroxy- 3-methylglutaryl-coA reductase antibody positivity', 'XPO:0100232', 'abnormal lymphatic system', 0.48148148148148145, 5.64885357140806, 1.6491871895674883, 'HP:0002715', 'Abnormality of the immune system'),
(405400, 'HP:0033708', 'Anti-3-hydroxy- 3-methylglutaryl-coA reductase antibody positivity', 'XPO:0100449', 'abnormal lymphocyte', 0.41935483870967744, 5.64885357140806, 1.5391147060347428, 'HP:0002715', 'Abnormality of the immune system'),
(405401, 'HP:0033708', 'Anti-3-hydroxy- 3-methylglutaryl-coA reductase antibody positivity', 'XPO:0100581', 'abnormal immune system', 0.48148148148148145, 5.64885357140806, 1.6491871895674883, 'HP:0002715', 'Abnormality of the immune system'),
(405402, 'HP:0033708', 'Anti-3-hydroxy- 3-methylglutaryl-coA reductase antibody positivity', 'XPO:0100004', 'abnormal cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(405403, 'HP:0033708', 'Anti-3-hydroxy- 3-methylglutaryl-coA reductase antibody positivity', 'XPO:0101083', 'abnormal T cell', 0.40625, 5.64885357140806, 1.5148751642906173, 'HP:0002715', 'Abnormality of the immune system'),
(405404, 'HP:0003189', 'Long nose', 'XPO:0133429', 'abnormal cilium morphology in the olfactory pit', 0.42857142857142855, 9.467216006125252, 2.01429349607732, 'UPHENO:0087950', 'abnormal nose morphology'),
(405405, 'HP:0003189', 'Long nose', 'XPO:0131462', 'increased size of the cilium in olfactory pit', 0.44776119402985076, 9.467216006125252, 2.0588958067471888, 'UPHENO:0087950', 'abnormal nose morphology'),
(405406, 'HP:0003189', 'Long nose', 'XPO:0103101', 'abnormal medial nasal prominence morphology', 0.42, 4.5318002188002176, 1.3796217205799897, 'UPHENO:0087907', 'abnormal head morphology'),
(405407, 'HP:0003189', 'Long nose', 'XPO:0101634', 'abnormal head morphology', 0.44680851063829785, 4.5318002188002176, 1.422971154406314, 'UPHENO:0087907', 'abnormal head morphology'),
(405408, 'HP:0003189', 'Long nose', 'XPO:0128440', 'decreased size of the Jacobsons organ', 0.4375, 9.467216006125252, 2.035167561327518, 'UPHENO:0087950', 'abnormal nose morphology'),
(405409, 'HP:0003189', 'Long nose', 'XPO:0141835', 'edematous head', 0.42857142857142855, 4.5318002188002176, 1.3936283915633758, 'UPHENO:0087907', 'abnormal head morphology'),
(405410, 'HP:0003189', 'Long nose', 'XPO:0140593', 'abnormally necrotic Jacobsons organ', 0.43548387096774194, 9.467216006125252, 2.030472820215821, 'UPHENO:0087950', 'abnormal nose morphology'),
(405411, 'HP:0003189', 'Long nose', 'XPO:0126234', 'absent nostril', 0.4603174603174603, 9.601025046317446, 2.1022653176431305, 'UPHENO:0021517', 'abnormal nose morphology'),
(405412, 'HP:0003189', 'Long nose', 'XPO:0141298', 'abnormal intercanthal region morphology', 0.42857142857142855, 4.5318002188002176, 1.3936283915633758, 'UPHENO:0087907', 'abnormal head morphology'),
(405413, 'HP:0003189', 'Long nose', 'XPO:0130273', 'increased size of the pharyngeal pouch', 0.4444444444444444, 5.972749669260594, 1.629280641436663, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(405414, 'HP:0003189', 'Long nose', 'XPO:0102804', 'abnormal pharyngeal pouch morphology', 0.42, 4.5318002188002176, 1.3796217205799897, 'UPHENO:0087907', 'abnormal head morphology'),
(405415, 'HP:0003189', 'Long nose', 'XPO:0141339', 'decreased pigmentation in the head', 0.42, 4.5318002188002176, 1.3796217205799897, 'UPHENO:0087907', 'abnormal head morphology'),
(405416, 'HP:0003189', 'Long nose', 'XPO:0142045', 'increased size of the nasal region', 0.4444444444444444, 5.972749669260594, 1.629280641436663, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(405417, 'HP:0003189', 'Long nose', 'XPO:0131491', 'decreased size of the cilium in the olfactory pit', 0.4057971014492754, 9.467216006125252, 1.9600430643431823, 'UPHENO:0087950', 'abnormal nose morphology'),
(405418, 'HP:0003189', 'Long nose', 'XPO:0102572', 'abnormal hatching gland primordium morphology', 0.40384615384615385, 4.5318002188002176, 1.3528303989641963, 'UPHENO:0087907', 'abnormal head morphology'),
(405419, 'HP:0003189', 'Long nose', 'XPO:0129920', 'increased size of the Jacobsons organ', 0.4918032786885246, 9.467216006125252, 2.1577784575495413, 'UPHENO:0087950', 'abnormal nose morphology'),
(405420, 'HP:0003189', 'Long nose', 'XPO:0103786', 'increased length of the anterior-posterior axis', 0.41304347826086957, 10.082766826679832, 2.0407403265935495, 'UPHENO:0055730', 'increased anatomical entity length in independent continuant'),
(405421, 'HP:0003189', 'Long nose', 'XPO:0127898', 'abnormally localised nostril', 0.5, 9.601025046317446, 2.191007193771559, 'UPHENO:0021517', 'abnormal nose morphology'),
(405422, 'HP:0003189', 'Long nose', 'XPO:0130703', 'increased size of the circumpharyngeal ridge', 0.4444444444444444, 5.972749669260594, 1.629280641436663, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(405423, 'HP:0003189', 'Long nose', 'XPO:0140223', 'abnormally necrotic head region', 0.40384615384615385, 4.5318002188002176, 1.3528303989641963, 'UPHENO:0087907', 'abnormal head morphology'),
(405424, 'HP:0003189', 'Long nose', 'XPO:0140914', 'abnormally necrotic intercanthal region', 0.40384615384615385, 4.5318002188002176, 1.3528303989641963, 'UPHENO:0087907', 'abnormal head morphology'),
(405425, 'HP:0003189', 'Long nose', 'XPO:0130640', 'increased size of the medial nasal prominence', 0.4528301886792453, 5.972749669260594, 1.6445793868540293, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(405426, 'HP:0003189', 'Long nose', 'XPO:0141828', 'increased width of craniofacial region', 0.42105263157894735, 5.972749669260594, 1.585825326448175, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(405427, 'HP:0003189', 'Long nose', 'XPO:0103115', 'abnormal nostril morphology', 0.5178571428571429, 9.601025046317446, 2.2297890929381237, 'UPHENO:0021517', 'abnormal nose morphology'),
(405428, 'HP:0003189', 'Long nose', 'XPO:0139715', 'abnormally necrotic head', 0.40384615384615385, 4.5318002188002176, 1.3528303989641963, 'UPHENO:0087907', 'abnormal head morphology'),
(405429, 'HP:0003189', 'Long nose', 'XPO:0130079', 'increased size of the olfactory pit', 0.5263157894736842, 9.467216006125252, 2.232206367337418, 'UPHENO:0087950', 'abnormal nose morphology'),
(405430, 'HP:0003189', 'Long nose', 'XPO:0102052', 'abnormal choana morphology', 0.4603174603174603, 9.601025046317446, 2.1022653176431305, 'UPHENO:0021517', 'abnormal nose morphology'),
(405431, 'HP:0003189', 'Long nose', 'XPO:0128582', 'decreased size of the head region', 0.41509433962264153, 4.6864066944795475, 1.3947404389520346, 'UPHENO:0075195', 'abnormal size of anatomical entity'),
(405432, 'HP:0003189', 'Long nose', 'XPO:0130048', 'increased size of the optic disc', 0.40298507462686567, 5.972749669260594, 1.5514280425448572, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(405433, 'HP:0003189', 'Long nose', 'XPO:0128599', 'decreased size of the olfactory pit', 0.4745762711864407, 9.467216006125252, 2.1196499877818296, 'UPHENO:0087950', 'abnormal nose morphology'),
(405434, 'HP:0003189', 'Long nose', 'XPO:0102226', 'abnormal Jacobsons organ morphology', 0.47368421052631576, 9.467216006125252, 2.117656898495018, 'UPHENO:0087950', 'abnormal nose morphology'),
(405435, 'HP:0003189', 'Long nose', 'XPO:0100420', 'abnormal choana', 0.58, 9.601025046317446, 2.359786966415426, 'UPHENO:0021517', 'abnormal nose morphology'),
(405436, 'HP:0003189', 'Long nose', 'XPO:0130324', 'increased size of the choana', 0.48484848484848486, 9.601025046317446, 2.1575547378222804, 'UPHENO:0021517', 'abnormal nose morphology'),
(405437, 'HP:0003189', 'Long nose', 'XPO:0140335', 'abnormally necrotic pharyngeal region', 0.42857142857142855, 4.5318002188002176, 1.3936283915633758, 'UPHENO:0087907', 'abnormal head morphology'),
(405438, 'HP:0003189', 'Long nose', 'XPO:0130319', 'increased size of the craniofacial region', 0.4444444444444444, 5.972749669260594, 1.629280641436663, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(405439, 'HP:0003189', 'Long nose', 'XPO:0131600', 'decreased size of the intercanthal region', 0.41509433962264153, 4.6864066944795475, 1.3947404389520346, 'UPHENO:0075195', 'abnormal size of anatomical entity'),
(405440, 'HP:0003189', 'Long nose', 'XPO:0102966', 'abnormal olfactory pit morphology', 0.4909090909090909, 9.467216006125252, 2.1558159483144523, 'UPHENO:0087950', 'abnormal nose morphology'),
(405441, 'HP:0003189', 'Long nose', 'XPO:0102259', 'abnormal pharyngeal region morphology', 0.45652173913043476, 4.5318002188002176, 1.4383550734357495, 'UPHENO:0087907', 'abnormal head morphology'),
(405442, 'HP:0003189', 'Long nose', 'XPO:0128846', 'decreased size of the choana', 0.4411764705882353, 9.601025046317446, 2.058092890023086, 'UPHENO:0021517', 'abnormal nose morphology'),
(405443, 'HP:0003189', 'Long nose', 'XPO:0102734', 'abnormal craniofacial region morphology', 0.42, 4.5318002188002176, 1.3796217205799897, 'UPHENO:0087907', 'abnormal head morphology'),
(405444, 'HP:0003189', 'Long nose', 'XPO:0130787', 'increased size of the lateral nasal prominence', 0.4528301886792453, 5.972749669260594, 1.6445793868540293, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(405445, 'HP:0003189', 'Long nose', 'XPO:0130295', 'increased size of the hatching gland primordium', 0.42857142857142855, 5.972749669260594, 1.5999218287949384, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(405446, 'HP:0003189', 'Long nose', 'XPO:0130062', 'increased size of the head region', 0.47058823529411764, 5.972749669260594, 1.6765159488388017, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(405447, 'HP:0003189', 'Long nose', 'XPO:0103358', 'decreased size of the pharyngeal region', 0.44, 4.6864066944795475, 1.4359731702128007, 'UPHENO:0075195', 'abnormal size of anatomical entity'),
(405448, 'HP:0003189', 'Long nose', 'XPO:0125246', 'absent choana', 0.46774193548387094, 9.601025046317446, 2.1191512541094477, 'UPHENO:0021517', 'abnormal nose morphology'),
(405449, 'HP:0003189', 'Long nose', 'XPO:0129460', 'decreased size of the nostril', 0.46153846153846156, 9.601025046317446, 2.1050516214738275, 'UPHENO:0021517', 'abnormal nose morphology'),
(405450, 'HP:0003189', 'Long nose', 'XPO:0102082', 'abnormal circumpharyngeal ridge morphology', 0.4117647058823529, 4.5318002188002176, 1.3660290568695288, 'UPHENO:0087907', 'abnormal head morphology'),
(405451, 'HP:0003189', 'Long nose', 'XPO:0103739', 'increased size of the pharyngeal region', 0.5, 5.972749669260594, 1.7281130850237483, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(405452, 'HP:0003189', 'Long nose', 'XPO:0130934', 'increased size of the nostril', 0.5161290322580645, 9.601025046317446, 2.2260655349385523, 'UPHENO:0021517', 'abnormal nose morphology'),
(405453, 'HP:0003189', 'Long nose', 'XPO:0131638', 'increased size of the intercanthal region', 0.47058823529411764, 5.972749669260594, 1.6765159488388017, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(405454, 'HP:0003189', 'Long nose', 'XPO:0142059', 'abnormal nasal region morphology', 0.4375, 4.5318002188002176, 1.4080705222839853, 'UPHENO:0087907', 'abnormal head morphology'),
(405455, 'HP:0003189', 'Long nose', 'XPO:0133370', 'olfactory pit fused with brain', 0.46551724137931033, 9.467216006125252, 2.099321861629007, 'UPHENO:0087950', 'abnormal nose morphology'),
(405456, 'HP:0003189', 'Long nose', 'XPO:0103707', 'increased pigmentation in the head', 0.42, 4.5318002188002176, 1.3796217205799897, 'UPHENO:0087907', 'abnormal head morphology'),
(405457, 'HP:0003189', 'Long nose', 'XPO:0141839', 'edematous pharyngeal region', 0.4375, 4.5318002188002176, 1.4080705222839853, 'UPHENO:0087907', 'abnormal head morphology'),
(405458, 'HP:0003189', 'Long nose', 'XPO:0101483', 'abnormal nostril', 0.6041666666666666, 9.601025046317446, 2.4084474872450072, 'UPHENO:0021517', 'abnormal nose morphology'),
(405459, 'HP:0003189', 'Long nose', 'XPO:0126871', 'abnormally localised choana', 0.5087719298245614, 9.601025046317446, 2.210142991100095, 'UPHENO:0021517', 'abnormal nose morphology'),
(405460, 'HP:0003189', 'Long nose', 'XPO:0115526', 'abnormally incomplete structure of head', 0.4375, 4.5318002188002176, 1.4080705222839853, 'UPHENO:0087907', 'abnormal head morphology'),
(405461, 'HP:0003189', 'Long nose', 'XPO:0102538', 'abnormal lateral nasal prominence morphology', 0.42, 4.5318002188002176, 1.3796217205799897, 'UPHENO:0087907', 'abnormal head morphology'),
(405462, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100023', 'abnormal mesenchyme', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(405463, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0101200', 'abnormal joint region', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(405464, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100258', 'abnormal organ part', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(405465, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100956', 'abnormal centrosome', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(405466, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0101366', 'abnormal morula cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(405467, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0141499', 'abnormal tadpole', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(405468, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100135', 'abnormal surface structure', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(405469, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0107285', 'abnormal flexural organ', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(405470, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100006', 'abnormal anatomical structure', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(405471, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0107288', 'abnormal larval alimentary system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(405472, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0101480', 'abnormal stage V oocyte', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(405473, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100781', 'abnormal presumptive ectoderm', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(405474, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0107284', 'abnormal migrating myoblast', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(405475, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100501', 'abnormal urogenital system', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(405476, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100638', 'abnormal polar body', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(405477, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0101074', 'abnormal germinal vesicle', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(405478, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100754', 'abnormal electrically active cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(405479, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0141745', 'abnormal creatinine homeostasis', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(405480, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100337', 'abnormal zygote', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(405481, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0101411', 'abnormal marginal zone (sensu neural)', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(405482, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100862', 'abnormal blastomere V1', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(405483, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100894', 'abnormal nucleus', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(405484, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100724', 'abnormal kinetochore', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(405485, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0131667', 'abnormal actin cytoskeleton', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(405486, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100384', 'abnormal amputated tissue', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(405487, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100991', 'abnormal iliac process primordium', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(405488, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100009', 'abnormal multi-tissue structure', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(405489, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100003', 'abnormal organism subdivision', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(405490, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0101078', 'abnormal mucous gland', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(405491, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0141714', 'abnormal anterior notochord', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(405492, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100907', 'abnormal cytoplasm', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(405493, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0141796', 'abnormal demethylation', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(405494, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0107276', 'abnormal dorsal region', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(405495, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100293', 'abnormal duct', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(405496, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100307', 'abnormal blastomere', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(405497, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100515', 'abnormal somatic stem cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(405498, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100429', 'abnormal spermatid', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(405499, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0107264', 'abnormal anterior side', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(405500, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100417', 'abnormal dense regular connective tissue', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(405501, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0141315', 'abnormal anatomical region', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(405502, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100643', 'abnormal thoracic region', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(405503, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0101132', 'abnormal apoptotic cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(405504, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100028', 'abnormal anatomical cluster', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(405505, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100626', 'abnormal primordial germ cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(405506, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0101297', 'abnormal barrier cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(405507, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0101157', 'abnormal female organism', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(405508, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0101240', 'abnormal ciliated non-epidermal cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(405509, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100032', 'abnormal nervous system', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(405510, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100667', 'abnormal vegetal yolk mass', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(405511, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0101109', 'abnormal egg cell-free extract', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(405512, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100852', 'abnormal interdigital region', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(405513, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100989', 'abnormal right blastomere', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(405514, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0141272', 'absent surface breathing', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(405515, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0101136', 'abnormal ooplasm', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(405516, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100069', 'abnormal urinary system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(405517, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0101451', 'abnormal dorsal lymph space', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(405518, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100802', 'abnormal exocrine cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(405519, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100164', 'abnormal neural nucleus', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(405520, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0142056', 'abnormal main body axis', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(405521, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100585', 'abnormal elastica externa', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(405522, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100915', 'abnormal dermal system', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(405523, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100031', 'abnormal central nervous system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(405524, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100251', 'abnormal proteinaceous extracellular matrix', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(405525, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100465', 'abnormal skeletal system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(405526, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100225', 'abnormal endocrine system', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(405527, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100372', 'abnormal hematological system', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(405528, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0101174', 'abnormal articular system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(405529, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100549', 'abnormal mitotic cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(405530, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100917', 'abnormal stage III oocyte', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(405531, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100202', 'abnormal embryo', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(405532, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0141787', 'abnormal hormone metabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(405533, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0101176', 'abnormal non-ciliated epithelial cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(405534, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100416', 'abnormal ligament', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(405535, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100493', 'abnormal liver and biliary system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(405536, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100581', 'abnormal immune system', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(405537, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100151', 'abnormal primordium', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(405538, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100010', 'abnormal multicellular anatomical structure', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(405539, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0141781', 'abnormal secondary metabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(405540, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100192', 'abnormal epithelium', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(405541, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0107312', 'abnormal filopodium', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(405542, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0141776', 'abnormal metabolic process', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(405543, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100823', 'abnormal blood', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(405544, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100640', 'abnormal notochordal sheath', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(405545, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100277', 'abnormal blastocoel', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(405546, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0101283', 'abnormal left-ventral blastomere', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(405547, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0141778', 'abnormal biosynthetic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(405548, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100104', 'abnormal embryonic structure', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(405549, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100377', 'abnormal connective tissue', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(405550, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100969', 'abnormal disaggregated/reaggregated ectoderm treated with activin', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(405551, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0101311', 'abnormal bottle cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(405552, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0141841', 'abnormality of whole organism mass', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(405553, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100999', 'abnormal serous membrane', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(405554, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100392', 'abnormal cilium', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(405555, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0101547', 'abnormal lampbrush chromosome', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(405556, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0131691', 'abnormal molecular function', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(405557, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100574', 'abnormal gastrula cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(405558, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100976', 'abnormal multiciliated cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(405559, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100688', 'abnormal adipose tissue', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(405560, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0101362', 'abnormal vegetal cortex', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(405561, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0141797', 'abnormal hydrogen metabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(405562, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0141266', 'abnormal surface breathing', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(405563, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0101072', 'abnormal mitochondrial cloud', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(405564, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0107339', 'abnormal yolk platelet', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(405565, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0107271', 'abnormal apical region', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(405566, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100888', 'abnormal microtubule', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(405567, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0141267', 'abnormal resting posture', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(405568, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0141271', 'increased surface breathing', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(405569, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100458', 'abnormal autopod', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(405570, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0101570', 'abnormal forelimb region', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(405571, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100762', 'abnormal intersomitic region', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(405572, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0101347', 'abnormal hindlimb region', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(405573, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0141794', 'abnormal prosthetic group metabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(405574, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0101220', 'abnormal centriole', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(405575, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100285', 'abnormal progenitor cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(405576, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100610', 'abnormal appendage', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(405577, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0101448', 'abnormal myelin accumulating cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(405578, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0141783', 'abnormal collagen metabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(405579, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0101096', 'abnormal tendon', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(405580, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100728', 'abnormal cell condensation', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(405581, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0101503', 'abnormal organ cortex', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(405582, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100084', 'abnormal anatomical group', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(405583, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100784', 'abnormal left blastomere', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(405584, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0101535', 'abnormal absorptive cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(405585, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100308', 'abnormal early embryonic cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(405586, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0107258', 'abnormal anatomical axis', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(405587, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0141264', 'abnormal schooling behavior', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(405588, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100423', 'abnormal process', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(405589, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0142051', 'abnormal cerebrospinal fluid', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(405590, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0141748', 'abnormal gas homeostasis', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(405591, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0101302', 'abnormal subcortical cytoplasm', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(405592, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100856', 'abnormal simple organ', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(405593, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0107269', 'abnormal right side', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(405594, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0141786', 'abnormal pigment metabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(405595, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0131685', 'abnormal cortical actin cytoskeleton', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(405596, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0101513', 'abnormal basal body', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(405597, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0101467', 'abnormal alkali secreting cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(405598, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100842', 'abnormal left-dorsal blastomere', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(405599, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0107253', 'abnormal enteric nervous system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(405600, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0141791', 'abnormal primary metabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(405601, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100912', 'abnormal trabecula', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(405602, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0101373', 'abnormal oxygen accumulating cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(405603, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0101519', 'abnormal hypobranchial placode', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(405604, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0115508', 'abnormally peramorphic growth of whole organism', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(405605, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100062', 'abnormal anatomical space', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(405606, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100176', 'abnormal stage VI oocyte', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(405607, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100386', 'abnormal limb', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(405608, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100721', 'abnormal centromere', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(405609, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100289', 'abnormal chondroblast', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(405610, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100014', 'abnormal tissue', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(405611, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100887', 'abnormal right-dorsal blastomere', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(405612, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0101264', 'abnormal mitotic spindle', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(405613, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100273', 'abnormal visual system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(405614, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0101435', 'abnormal paracrine cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(405615, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100026', 'abnormal germ cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(405616, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0107268', 'abnormal left side', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(405617, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100422', 'abnormal notochord', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(405618, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0141743', 'abnormal chemical homeostasis within a tissue', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(405619, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:00000000', 'Xenopus phenotype', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(405620, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0107267', 'abnormal ventral side', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(405621, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0101004', 'abnormal acid secreting cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(405622, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100394', 'abnormal marginal zone', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(405623, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0131666', 'abnormal adherens junction', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(405624, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0107261', 'abnormal dorsal-ventral axis', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(405625, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100745', 'abnormal anterior lymph sac', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(405626, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0107278', 'abnormal medial region', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(405627, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100511', 'abnormal stylopod', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(405628, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0107259', 'abnormal animal-vegetal axis', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(405629, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100674', 'abnormal secondary oogonium', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(405630, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100205', 'abnormal limb segment', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(405631, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0141718', 'abnormal posterior notochord', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(405632, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0101113', 'abnormal stage IV oocyte', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(405633, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100786', 'abnormal presumptive axial mesoderm', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(405634, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100231', 'abnormal compound organ', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(405635, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0141772', 'abnormal water homeostasis', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(405636, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100004', 'abnormal cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(405637, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100902', 'abnormal spermatocyte', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(405638, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100274', 'abnormal sensory system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(405639, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100295', 'abnormal extracellular matrix', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(405640, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0142052', 'abnormal nasal region', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(405641, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0115512', 'abnormally semi-erect whole organism', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(405642, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100573', 'abnormal extraembryonic structure', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(405643, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100587', 'abnormal vestibuloauditory system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(405644, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100704', 'abnormal Merkel cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(405645, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100025', 'abnormal oocyte', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(405646, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0141715', 'abnormal septum', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(405647, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0141782', 'abnormal methylation', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(405648, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0115509', 'abnormally semi-viable whole organism', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(405649, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100913', 'abnormal Brachets cleft', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(405650, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0107272', 'abnormal axial region', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(405651, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0101168', 'abnormal circulating cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(405652, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100402', 'abnormal zeugopod', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(405653, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100427', 'abnormal olfactory system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(405654, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0101040', 'abnormal axial mesoderm', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(405655, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100317', 'abnormal respiratory system', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(405656, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0115758', 'abnormally decreased mobility of melanoblast', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(405657, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100415', 'abnormal secretory epithelial cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(405658, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100665', 'abnormal egg jelly', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(405659, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0101389', 'abnormal wedge region', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(405660, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0107263', 'abnormal anatomical side', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(405661, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100742', 'abnormal musculoskeletal system', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(405662, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100547', 'abnormal blastomere V2', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(405663, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0141770', 'abnormal urate homeostasis', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(405664, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0101468', 'abnormal stage I oocyte', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(405665, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100282', 'abnormal pelvic girdle primordium', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(405666, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100363', 'abnormal cardiovascular system', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(405667, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0101378', 'abnormal blastomere D1', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(405668, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0101228', 'abnormal mesenchymal stem cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(405669, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100186', 'abnormal uveal tract', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(405670, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0101472', 'abnormal zygote cortex', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(405671, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0107273', 'abnormal basal region', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(405672, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100108', 'abnormal cell part', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(405673, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0101071', 'abnormal endoplasmic reticulum', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(405674, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0116494', 'absent biological process', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(405675, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0141263', 'abnormal visually guided collision avoidance behavior', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(405676, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0101061', 'abnormal plasma membrane', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(405677, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0131675', 'abnormal spindle microtubule', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(405678, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100531', 'abnormal proliferative region', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(405679, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0142057', 'abnormal desmosome', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(405680, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100218', 'abnormal epithelial cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(405681, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100339', 'abnormal circumblastoporal collar', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(405682, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0101023', 'abnormal ultimobranchial body', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(405683, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100900', 'abnormal angioblast', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(405684, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100172', 'abnormal stem cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(405685, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100691', 'abnormal keratin accumulating cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(405686, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100807', 'abnormal matrix-based tissue', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(405687, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100653', 'abnormal myoblast', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(405688, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100002', 'abnormal head', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(405689, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0141775', 'abnormal nitrogen compound metabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(405690, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0101221', 'abnormal larval immune system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(405691, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100437', 'abnormal proepicardium', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(405692, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0131687', 'abnormal astral microtubule', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(405693, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0116434', 'abnormal biological process', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(405694, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100481', 'abnormal anatomical line', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(405695, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0101333', 'abnormal barrier epithelial cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(405696, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100162', 'abnormal presumptive rhombomere', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(405697, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0141276', 'decreased surface breathing', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(405698, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100232', 'abnormal lymphatic system', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(405699, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0101497', 'abnormal ciliary axoneme', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(405700, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100503', 'abnormal blastomere D2', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(405701, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100599', 'abnormal adult immune system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(405702, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100557', 'abnormal prime meridian', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(405703, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100114', 'abnormal peripheral nervous system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(405704, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0107260', 'abnormal anterior-posterior axis', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(405705, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0107266', 'abnormal dorsal side', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(405706, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0141771', 'abnormal urea homeostasis', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(405707, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0101461', 'abnormal sperm entry point', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(405708, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0107265', 'abnormal posterior side', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(405709, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100545', 'abnormal male organism', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(405710, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100239', 'abnormal acellular anatomical structure', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(405711, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100152', 'abnormal alimentary system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(405712, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0101463', 'abnormal right-ventral blastomere', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(405713, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0131723', 'abnormal pathway-restricted SMAD protein phosphorylation', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(405714, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100265', 'abnormal sensory epithelial cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(405715, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100120', 'abnormal genital system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(405716, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100715', 'abnormal ciliated cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(405717, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0131725', 'abnormal phosphorylation of RNA polymerase II C-terminal domain', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(405718, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0101326', 'abnormal cementoblast', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(405719, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0101498', 'abnormal stage II oocyte', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(405720, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0131677', 'abnormal actin filament', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(405721, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100899', 'abnormal secondary spermatogonium', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(405722, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0101409', 'abnormal perivitelline space', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(405723, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0141777', 'abnormal catabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(405724, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0141265', 'abnormal escape behavior', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(405725, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0131669', 'abnormal Roux spot', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(405726, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0101237', 'abnormal mucus secreting cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(405727, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0107262', 'abnormal left-right axis', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(405728, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0115391', 'abnormally undifferentiated alimentary system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(405729, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0101110', 'abnormal cell-free extract', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(405730, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100081', 'abnormal anatomical entity in vitro', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(405731, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100551', 'abnormal oocyte cortex', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(405732, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0101241', 'abnormal nucleate erythrocyte', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(405733, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0115505', 'dead whole organism', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(405734, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100070', 'abnormal anatomical system', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(405735, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0107270', 'abnormal proximal-distal axis', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(405736, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0141784', 'abnormal cellular hormone metabolic process', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(405737, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0101141', 'abnormal Keller explant', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(405738, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0141904', 'abnormal glucosamine metabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(405739, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0141738', 'abnormal carbon dioxide homeostasis', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(405740, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100533', 'abnormal melanoblast', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(405741, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0101575', 'abnormal vitelline membrane', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(405742, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100791', 'abnormal multiciliated cell precursor', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(405743, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100546', 'abnormal whole organism', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(405744, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100060', 'abnormal regenerating tissue', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(405745, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0101406', 'abnormal cleavage furrow', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(405746, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0101405', 'abnormal ring structure', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(405747, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0101569', 'abnormal activin-induced ectoderm', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(405748, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100477', 'abnormal pericyte', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(405749, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100268', 'abnormal circulatory system', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(405750, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100642', 'abnormal gustatory system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(405751, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0141792', 'abnormal small molecule metabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(405752, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0100344', 'abnormal portion of organism substance', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(405753, 'HP:0001557', 'Prenatal movement abnormality', 'XPO:0101212', 'abnormal glomeral mesenchyme', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(405754, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0139981', 'abnormally necrotic early embryonic cell', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(405755, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0140522', 'abnormally necrotic stage II oocyte', 0.4090909090909091, 5.43643956286526, 1.491307481034791, 'HP:0025461', 'Abnormal cell morphology'),
(405756, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0107373', 'abnormal efferent neuron morphology', 0.4090909090909091, 5.43643956286526, 1.491307481034791, 'HP:0025461', 'Abnormal cell morphology'),
(405757, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0101061', 'abnormal plasma membrane', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(405758, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0100724', 'abnormal kinetochore', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(405759, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0101658', 'abnormal germ cell morphology', 0.5294117647058824, 5.43643956286526, 1.696500828969256, 'HP:0025461', 'Abnormal cell morphology'),
(405760, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0101940', 'abnormal early embryonic cell morphology', 0.5, 5.43643956286526, 1.6487024538808177, 'HP:0025461', 'Abnormal cell morphology'),
(405761, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0101969', 'abnormal zygote morphology', 0.5294117647058824, 5.43643956286526, 1.696500828969256, 'HP:0025461', 'Abnormal cell morphology'),
(405762, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0129507', 'increased size of the circulating cell', 0.44, 5.9590888072311134, 1.6192588042625211, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(405763, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0101828', 'abnormal neuron morphology', 0.43902439024390244, 5.43643956286526, 1.5449043867452603, 'HP:0025461', 'Abnormal cell morphology'),
(405764, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0102703', 'abnormal endoplasmic reticulum morphology', 0.45714285714285713, 3.6715585125471644, 1.2955411026258445, 'UPHENO:0086172', 'abnormal cell'),
(405765, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0101657', 'abnormal oocyte morphology', 0.5, 5.43643956286526, 1.6487024538808177, 'HP:0025461', 'Abnormal cell morphology'),
(405766, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0140752', 'abnormally necrotic melanoblast', 0.47368421052631576, 5.43643956286526, 1.6047291305419304, 'HP:0025461', 'Abnormal cell morphology'),
(405767, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0139990', 'abnormally necrotic cardiovascular system', 0.4186046511627907, 5.9590888072311134, 1.5793993451306325, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(405768, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0102165', 'abnormal melanoblast morphology', 0.5294117647058824, 5.43643956286526, 1.696500828969256, 'HP:0025461', 'Abnormal cell morphology'),
(405769, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0102519', 'abnormal right-dorsal blastomere morphology', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(405770, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0140938', 'abnormally necrotic secretory epithelial cell', 0.4090909090909091, 5.43643956286526, 1.491307481034791, 'HP:0025461', 'Abnormal cell morphology'),
(405771, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0102588', 'abnormal centrosome morphology', 0.45714285714285713, 3.6715585125471644, 1.2955411026258445, 'UPHENO:0086172', 'abnormal cell'),
(405772, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0107426', 'abnormal yolk platelet morphology', 0.43243243243243246, 3.6715585125471644, 1.2600400701560144, 'UPHENO:0086172', 'abnormal cell'),
(405773, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0100172', 'abnormal stem cell', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(405774, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0100802', 'abnormal exocrine cell', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(405775, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0103041', 'abnormal perivitelline space morphology', 0.43243243243243246, 3.6715585125471644, 1.2600400701560144, 'UPHENO:0086172', 'abnormal cell'),
(405776, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0140278', 'abnormally necrotic Merkel cell', 0.47368421052631576, 5.43643956286526, 1.6047291305419304, 'HP:0025461', 'Abnormal cell morphology'),
(405777, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0102990', 'abnormal endothelial cell morphology', 0.5, 5.9590888072311134, 1.7261356851694936, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(405778, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0102183', 'abnormal oocyte cortex morphology', 0.43243243243243246, 3.6715585125471644, 1.2600400701560144, 'UPHENO:0086172', 'abnormal cell'),
(405779, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0102958', 'abnormal cementoblast morphology', 0.5294117647058824, 5.43643956286526, 1.696500828969256, 'HP:0025461', 'Abnormal cell morphology'),
(405780, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0102356', 'abnormal kinetochore morphology', 0.45714285714285713, 3.6715585125471644, 1.2955411026258445, 'UPHENO:0086172', 'abnormal cell'),
(405781, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0140919', 'abnormally necrotic cementoblast', 0.47368421052631576, 5.43643956286526, 1.6047291305419304, 'HP:0025461', 'Abnormal cell morphology'),
(405782, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0140098', 'abnormally necrotic secondary spermatogonium', 0.43902439024390244, 5.43643956286526, 1.5449043867452603, 'HP:0025461', 'Abnormal cell morphology'),
(405783, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0140709', 'abnormally necrotic acid secreting cell', 0.47368421052631576, 5.43643956286526, 1.6047291305419304, 'HP:0025461', 'Abnormal cell morphology'),
(405784, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0141328', 'edematous circulatory system', 0.45, 5.9590888072311134, 1.6375560946892784, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(405785, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0140458', 'abnormally necrotic embryonic thrombocyte', 0.43137254901960786, 5.9590888072311134, 1.6033051264838831, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(405786, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0101071', 'abnormal endoplasmic reticulum', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(405787, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0140471', 'abnormally necrotic multiciliated cell precursor', 0.47368421052631576, 5.43643956286526, 1.6047291305419304, 'HP:0025461', 'Abnormal cell morphology'),
(405788, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0101373', 'abnormal oxygen accumulating cell', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(405789, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0102336', 'abnormal Merkel cell morphology', 0.5294117647058824, 5.43643956286526, 1.696500828969256, 'HP:0025461', 'Abnormal cell morphology'),
(405790, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0100902', 'abnormal spermatocyte', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(405791, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0101333', 'abnormal barrier epithelial cell', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(405792, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0102873', 'abnormal nucleate erythrocyte morphology', 0.5294117647058824, 5.43643956286526, 1.696500828969256, 'HP:0025461', 'Abnormal cell morphology'),
(405793, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0140600', 'abnormally necrotic apoptotic cell', 0.47368421052631576, 5.43643956286526, 1.6047291305419304, 'HP:0025461', 'Abnormal cell morphology'),
(405794, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0103179', 'abnormal lampbrush chromosome morphology', 0.45714285714285713, 3.6715585125471644, 1.2955411026258445, 'UPHENO:0086172', 'abnormal cell'),
(405795, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0102135', 'abnormal blastomere D2 morphology', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(405796, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0140767', 'abnormally necrotic stage IV oocyte', 0.4090909090909091, 5.43643956286526, 1.491307481034791, 'HP:0025461', 'Abnormal cell morphology'),
(405797, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0107312', 'abnormal filopodium', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(405798, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0140459', 'abnormally necrotic thrombocyte', 0.4583333333333333, 5.9590888072311134, 1.652649096646833, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(405799, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0101467', 'abnormal alkali secreting cell', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(405800, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0103207', 'abnormal vitelline membrane morphology', 0.41025641025641024, 3.6715585125471644, 1.2273061620492112, 'UPHENO:0086172', 'abnormal cell'),
(405801, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0101132', 'abnormal apoptotic cell', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(405802, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0102706', 'abnormal germinal vesicle morphology', 0.41025641025641024, 3.6715585125471644, 1.2273061620492112, 'UPHENO:0086172', 'abnormal cell'),
(405803, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0101807', 'abnormal migrating neuroblast morphology', 0.43902439024390244, 5.43643956286526, 1.5449043867452603, 'HP:0025461', 'Abnormal cell morphology'),
(405804, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0141289', 'abnormal spindle microtubule morphology', 0.43243243243243246, 3.6715585125471644, 1.2600400701560144, 'UPHENO:0086172', 'abnormal cell'),
(405805, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0103005', 'abnormal oxygen accumulating cell morphology', 0.5294117647058824, 5.43643956286526, 1.696500828969256, 'HP:0025461', 'Abnormal cell morphology'),
(405806, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0101237', 'abnormal mucus secreting cell', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(405807, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0103082', 'abnormal myeloid cell morphology', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(405808, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0103112', 'abnormal stage V oocyte morphology', 0.47368421052631576, 5.43643956286526, 1.6047291305419304, 'HP:0025461', 'Abnormal cell morphology'),
(405809, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0131667', 'abnormal actin cytoskeleton', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(405810, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0140328', 'abnormally necrotic secondary oogonium', 0.43902439024390244, 5.43643956286526, 1.5449043867452603, 'HP:0025461', 'Abnormal cell morphology'),
(405811, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0101638', 'abnormal anatomical structure morphology', 0.41379310344827586, 2.7446671847279203, 1.0657036887902793, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(405812, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0141112', 'abnormally necrotic angioblast', 0.5238095238095238, 5.9590888072311134, 1.7667562000611157, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(405813, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0107411', 'abnormal embryonic thrombocyte morphology', 0.4782608695652174, 5.9590888072311134, 1.6881940038877956, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(405814, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0102069', 'abnormal proepicardium morphology', 0.5, 5.43643956286526, 1.6487024538808177, 'HP:0025461', 'Abnormal cell morphology'),
(405815, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0100289', 'abnormal chondroblast', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(405816, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0131666', 'abnormal adherens junction', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(405817, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0140505', 'abnormally necrotic stromal cell', 0.4090909090909091, 5.43643956286526, 1.491307481034791, 'HP:0025461', 'Abnormal cell morphology'),
(405818, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0102636', 'abnormal acid secreting cell morphology', 0.5294117647058824, 5.43643956286526, 1.696500828969256, 'HP:0025461', 'Abnormal cell morphology'),
(405819, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0141048', 'abnormally necrotic mitotic cell', 0.47368421052631576, 5.43643956286526, 1.6047291305419304, 'HP:0025461', 'Abnormal cell morphology'),
(405820, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0103093', 'abnormal sperm entry point morphology', 0.4444444444444444, 3.6715585125471644, 1.2774207542365574, 'UPHENO:0086172', 'abnormal cell'),
(405821, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0103219', 'abnormal hemangioblast morphology', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(405822, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0100888', 'abnormal microtubule', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(405823, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0128006', 'decreased size of the cell', 0.4186046511627907, 5.43643956286526, 1.5085486027240909, 'HP:0025461', 'Abnormal cell morphology'),
(405824, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0141314', 'abnormal Roux spot morphology', 0.43243243243243246, 3.6715585125471644, 1.2600400701560144, 'UPHENO:0086172', 'abnormal cell'),
(405825, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0100549', 'abnormal mitotic cell', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(405826, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0100976', 'abnormal multiciliated cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(405827, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0100638', 'abnormal polar body', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(405828, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0101240', 'abnormal ciliated non-epidermal cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(405829, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0140589', 'abnormally necrotic keratin accumulating cell', 0.47368421052631576, 5.43643956286526, 1.6047291305419304, 'HP:0025461', 'Abnormal cell morphology'),
(405830, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0139929', 'abnormally necrotic barrier epithelial cell', 0.47368421052631576, 5.43643956286526, 1.6047291305419304, 'HP:0025461', 'Abnormal cell morphology'),
(405831, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0140747', 'abnormally necrotic morula cell', 0.4186046511627907, 5.43643956286526, 1.5085486027240909, 'HP:0025461', 'Abnormal cell morphology'),
(405832, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0100956', 'abnormal centrosome', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(405833, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0102715', 'abnormal T cell morphology', 0.42857142857142855, 5.43643956286526, 1.526401870347189, 'HP:0025461', 'Abnormal cell morphology'),
(405834, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0102739', 'abnormal erythroid cell morphology', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(405835, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0102423', 'abnormal multiciliated cell precursor morphology', 0.5294117647058824, 5.43643956286526, 1.696500828969256, 'HP:0025461', 'Abnormal cell morphology'),
(405836, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0101835', 'abnormal endocrine cell morphology', 0.43902439024390244, 5.43643956286526, 1.5449043867452603, 'HP:0025461', 'Abnormal cell morphology'),
(405837, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0102549', 'abnormal stage III oocyte morphology', 0.47368421052631576, 5.43643956286526, 1.6047291305419304, 'HP:0025461', 'Abnormal cell morphology'),
(405838, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0101917', 'abnormal progenitor cell morphology', 0.5294117647058824, 5.43643956286526, 1.696500828969256, 'HP:0025461', 'Abnormal cell morphology'),
(405839, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0102704', 'abnormal mitochondrial cloud morphology', 0.43243243243243246, 3.6715585125471644, 1.2600400701560144, 'UPHENO:0086172', 'abnormal cell'),
(405840, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0102929', 'abnormal barrier cell morphology', 0.5294117647058824, 5.43643956286526, 1.696500828969256, 'HP:0025461', 'Abnormal cell morphology'),
(405841, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0102994', 'abnormal vegetal cortex morphology', 0.42105263157894735, 3.6715585125471644, 1.2433500608051093, 'UPHENO:0086172', 'abnormal cell'),
(405842, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0101919', 'abnormal heart primordium morphology', 0.42857142857142855, 5.9590888072311134, 1.598091112264582, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(405843, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0140358', 'abnormally necrotic non-ciliated epithelial cell', 0.4090909090909091, 5.43643956286526, 1.491307481034791, 'HP:0025461', 'Abnormal cell morphology'),
(405844, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0139759', 'abnormally necrotic germ cell', 0.47368421052631576, 5.43643956286526, 1.6047291305419304, 'HP:0025461', 'Abnormal cell morphology'),
(405845, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0101995', 'abnormal cardiovascular system morphology', 0.4864864864864865, 5.9590888072311134, 1.7026497515610226, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(405846, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0141146', 'abnormally necrotic oxygen accumulating cell', 0.47368421052631576, 5.43643956286526, 1.6047291305419304, 'HP:0025461', 'Abnormal cell morphology'),
(405847, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0140169', 'abnormally necrotic stage VI oocyte', 0.4090909090909091, 5.43643956286526, 1.491307481034791, 'HP:0025461', 'Abnormal cell morphology'),
(405848, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0100533', 'abnormal melanoblast', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(405849, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0101850', 'abnormal epithelial cell morphology', 0.4864864864864865, 5.43643956286526, 1.626270082715184, 'HP:0025461', 'Abnormal cell morphology'),
(405850, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0141166', 'abnormally necrotic stage III oocyte', 0.4090909090909091, 5.43643956286526, 1.491307481034791, 'HP:0025461', 'Abnormal cell morphology'),
(405851, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0100308', 'abnormal early embryonic cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(405852, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0103095', 'abnormal right-ventral blastomere morphology', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(405853, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0107284', 'abnormal migrating myoblast', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(405854, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0101804', 'abnormal stem cell morphology', 0.5294117647058824, 5.43643956286526, 1.696500828969256, 'HP:0025461', 'Abnormal cell morphology'),
(405855, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0102934', 'abnormal subcortical cytoplasm morphology', 0.43243243243243246, 3.6715585125471644, 1.2600400701560144, 'UPHENO:0086172', 'abnormal cell'),
(405856, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0102943', 'abnormal bottle cell morphology', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(405857, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0102745', 'abnormal stage IV oocyte morphology', 0.47368421052631576, 5.43643956286526, 1.6047291305419304, 'HP:0025461', 'Abnormal cell morphology'),
(405858, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0103010', 'abnormal blastomere D1 morphology', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(405859, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0131675', 'abnormal spindle microtubule', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(405860, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0103145', 'abnormal basal body morphology', 0.45714285714285713, 3.6715585125471644, 1.2955411026258445, 'UPHENO:0086172', 'abnormal cell'),
(405861, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0100429', 'abnormal spermatid', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(405862, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0140239', 'abnormally necrotic absorptive cell', 0.47368421052631576, 5.43643956286526, 1.6047291305419304, 'HP:0025461', 'Abnormal cell morphology'),
(405863, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0100907', 'abnormal cytoplasm', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(405864, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0101435', 'abnormal paracrine cell', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(405865, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0102869', 'abnormal mucus secreting cell morphology', 0.5294117647058824, 5.43643956286526, 1.696500828969256, 'HP:0025461', 'Abnormal cell morphology'),
(405866, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0107399', 'abnormal filopodium morphology', 0.45714285714285713, 3.6715585125471644, 1.2955411026258445, 'UPHENO:0086172', 'abnormal cell'),
(405867, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0102496', 'abnormal dorsolateral ascending neuron morphology', 0.4186046511627907, 5.43643956286526, 1.5085486027240909, 'HP:0025461', 'Abnormal cell morphology'),
(405868, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0103100', 'abnormal stage I oocyte morphology', 0.47368421052631576, 5.43643956286526, 1.6047291305419304, 'HP:0025461', 'Abnormal cell morphology'),
(405869, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0102179', 'abnormal blastomere V2 morphology', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(405870, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0102520', 'abnormal microtubule morphology', 0.45714285714285713, 3.6715585125471644, 1.2955411026258445, 'UPHENO:0086172', 'abnormal cell'),
(405871, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0102764', 'abnormal apoptotic cell morphology', 0.5294117647058824, 5.43643956286526, 1.696500828969256, 'HP:0025461', 'Abnormal cell morphology'),
(405872, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0140096', 'abnormally necrotic gastrula cell', 0.4186046511627907, 5.43643956286526, 1.5085486027240909, 'HP:0025461', 'Abnormal cell morphology'),
(405873, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0141065', 'abnormally necrotic paracrine cell', 0.47368421052631576, 5.43643956286526, 1.6047291305419304, 'HP:0025461', 'Abnormal cell morphology'),
(405874, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0101448', 'abnormal myelin accumulating cell', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(405875, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0139734', 'abnormally necrotic blastomere', 0.4186046511627907, 5.43643956286526, 1.5085486027240909, 'HP:0025461', 'Abnormal cell morphology'),
(405876, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0102752', 'abnormal cardiac progenitor cell morphology', 0.4888888888888889, 5.9590888072311134, 1.7068486475834443, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(405877, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0140450', 'abnormally necrotic mesenchymal stem cell', 0.43902439024390244, 5.43643956286526, 1.5449043867452603, 'HP:0025461', 'Abnormal cell morphology'),
(405878, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0100721', 'abnormal centromere', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(405879, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0100025', 'abnormal oocyte', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(405880, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0102306', 'abnormal secondary oogonium morphology', 0.5, 5.43643956286526, 1.6487024538808177, 'HP:0025461', 'Abnormal cell morphology'),
(405881, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0141285', 'abnormal cortical actin cytoskeleton morphology', 0.4444444444444444, 3.6715585125471644, 1.2774207542365574, 'UPHENO:0086172', 'abnormal cell'),
(405882, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0102768', 'abnormal ooplasm morphology', 0.43243243243243246, 3.6715585125471644, 1.2600400701560144, 'UPHENO:0086172', 'abnormal cell'),
(405883, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0102353', 'abnormal centromere morphology', 0.45714285714285713, 3.6715585125471644, 1.2955411026258445, 'UPHENO:0086172', 'abnormal cell'),
(405884, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0100899', 'abnormal secondary spermatogonium', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(405885, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0141261', 'abnormally necrotic adult thrombocyte', 0.43137254901960786, 5.9590888072311134, 1.6033051264838831, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(405886, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0100704', 'abnormal Merkel cell', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(405887, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0141246', 'abnormally necrotic stage V oocyte', 0.4090909090909091, 5.43643956286526, 1.491307481034791, 'HP:0025461', 'Abnormal cell morphology'),
(405888, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0101220', 'abnormal centriole', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(405889, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0101740', 'abnormal cell part morphology', 0.48484848484848486, 3.6715585125471644, 1.3342224633999569, 'UPHENO:0086172', 'abnormal cell'),
(405890, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0102334', 'abnormal glial cell morphology', 0.43902439024390244, 5.43643956286526, 1.5449043867452603, 'HP:0025461', 'Abnormal cell morphology'),
(405891, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0102901', 'abnormal mesodermal cell morphology', 0.4090909090909091, 5.43643956286526, 1.491307481034791, 'HP:0025461', 'Abnormal cell morphology'),
(405892, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0141135', 'abnormally necrotic spermatid', 0.43902439024390244, 5.43643956286526, 1.5449043867452603, 'HP:0025461', 'Abnormal cell morphology'),
(405893, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0141299', 'abnormal actin filament morphology', 0.4444444444444444, 3.6715585125471644, 1.2774207542365574, 'UPHENO:0086172', 'abnormal cell'),
(405894, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0102386', 'abnormal electrically active cell morphology', 0.5294117647058824, 5.43643956286526, 1.696500828969256, 'HP:0025461', 'Abnormal cell morphology'),
(405895, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0141195', 'abnormally necrotic somatic stem cell', 0.43902439024390244, 5.43643956286526, 1.5449043867452603, 'HP:0025461', 'Abnormal cell morphology'),
(405896, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0140381', 'abnormally necrotic ciliated cell', 0.47368421052631576, 5.43643956286526, 1.6047291305419304, 'HP:0025461', 'Abnormal cell morphology'),
(405897, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0101808', 'abnormal stage VI oocyte morphology', 0.47368421052631576, 5.43643956286526, 1.6047291305419304, 'HP:0025461', 'Abnormal cell morphology'),
(405898, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0101900', 'abnormal circulatory system morphology', 0.4864864864864865, 5.9590888072311134, 1.7026497515610226, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(405899, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0102965', 'abnormal barrier epithelial cell morphology', 0.5294117647058824, 5.43643956286526, 1.696500828969256, 'HP:0025461', 'Abnormal cell morphology'),
(405900, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0140104', 'abnormally necrotic circulating cell', 0.5238095238095238, 5.9590888072311134, 1.7667562000611157, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(405901, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0102181', 'abnormal mitotic cell morphology', 0.5294117647058824, 5.43643956286526, 1.696500828969256, 'HP:0025461', 'Abnormal cell morphology'),
(405902, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0139811', 'abnormally necrotic circulatory system', 0.4186046511627907, 5.9590888072311134, 1.5793993451306325, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(405903, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0100392', 'abnormal cilium', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(405904, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0139969', 'abnormally necrotic primordial germ cell', 0.43902439024390244, 5.43643956286526, 1.5449043867452603, 'HP:0025461', 'Abnormal cell morphology'),
(405905, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0100437', 'abnormal proepicardium', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(405906, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0100674', 'abnormal secondary oogonium', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(405907, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0102347', 'abnormal ciliated cell morphology', 0.5294117647058824, 5.43643956286526, 1.696500828969256, 'HP:0025461', 'Abnormal cell morphology'),
(405908, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0131685', 'abnormal cortical actin cytoskeleton', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(405909, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0140059', 'abnormally necrotic epithelial cell', 0.43902439024390244, 5.43643956286526, 1.5449043867452603, 'HP:0025461', 'Abnormal cell morphology'),
(405910, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0133436', 'abnormal cilium morphology in the multiciliated cell', 0.42105263157894735, 3.6715585125471644, 1.2433500608051093, 'UPHENO:0086172', 'abnormal cell'),
(405911, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0100337', 'abnormal zygote', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(405912, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0102161', 'abnormal epicardial precursor cell morphology', 0.46153846153846156, 7.414388317771038, 1.849871719182924, 'UPHENO:0076810', 'abnormal heart morphology'),
(405913, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0101297', 'abnormal barrier cell', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(405914, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0103037', 'abnormal ring structure morphology', 0.43243243243243246, 3.6715585125471644, 1.2600400701560144, 'UPHENO:0086172', 'abnormal cell'),
(405915, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0101535', 'abnormal absorptive cell', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(405916, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0101264', 'abnormal mitotic spindle', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(405917, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0101636', 'abnormal cell morphology', 0.5625, 5.43643956286526, 1.748713027947041, 'HP:0025461', 'Abnormal cell morphology'),
(405918, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0101976', 'abnormal portion of organism substance morphology', 0.41379310344827586, 2.7446671847279203, 1.0657036887902793, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(405919, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0107371', 'abnormal migrating myoblast morphology', 0.5, 5.43643956286526, 1.6487024538808177, 'HP:0025461', 'Abnormal cell morphology'),
(405920, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0100754', 'abnormal electrically active cell', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(405921, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0103132', 'abnormal endodermal cell morphology', 0.4090909090909091, 5.43643956286526, 1.491307481034791, 'HP:0025461', 'Abnormal cell morphology'),
(405922, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0102860', 'abnormal mesenchymal stem cell morphology', 0.5, 5.43643956286526, 1.6487024538808177, 'HP:0025461', 'Abnormal cell morphology'),
(405923, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0102608', 'abnormal multiciliated cell morphology', 0.5, 5.43643956286526, 1.6487024538808177, 'HP:0025461', 'Abnormal cell morphology'),
(405924, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0101921', 'abnormal chondroblast morphology', 0.5294117647058824, 5.43643956286526, 1.696500828969256, 'HP:0025461', 'Abnormal cell morphology'),
(405925, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0131677', 'abnormal actin filament', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(405926, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0140647', 'abnormally necrotic nucleate erythrocyte', 0.47368421052631576, 5.43643956286526, 1.6047291305419304, 'HP:0025461', 'Abnormal cell morphology'),
(405927, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0101468', 'abnormal stage I oocyte', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(405928, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0102206', 'abnormal gastrula cell morphology', 0.47368421052631576, 5.43643956286526, 1.6047291305419304, 'HP:0025461', 'Abnormal cell morphology'),
(405929, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0107398', 'abnormal apical junction complex morphology', 0.41025641025641024, 3.6715585125471644, 1.2273061620492112, 'UPHENO:0086172', 'abnormal cell'),
(405930, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0101821', 'abnormal enteroendocrine cell morphology', 0.4186046511627907, 5.43643956286526, 1.5085486027240909, 'HP:0025461', 'Abnormal cell morphology'),
(405931, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0140331', 'abnormally necrotic myeloid cell', 0.4090909090909091, 5.43643956286526, 1.491307481034791, 'HP:0025461', 'Abnormal cell morphology'),
(405932, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0141288', 'abnormal astral microtubule morphology', 0.41025641025641024, 3.6715585125471644, 1.2273061620492112, 'UPHENO:0086172', 'abnormal cell'),
(405933, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0100894', 'abnormal nucleus', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(405934, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0102531', 'abnormal secondary spermatogonium morphology', 0.5, 5.43643956286526, 1.6487024538808177, 'HP:0025461', 'Abnormal cell morphology'),
(405935, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0140580', 'abnormally necrotic migrating myoblast', 0.43902439024390244, 5.43643956286526, 1.5449043867452603, 'HP:0025461', 'Abnormal cell morphology'),
(405936, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0102586', 'abnormal neural progenitor cell morphology', 0.4186046511627907, 5.43643956286526, 1.5085486027240909, 'HP:0025461', 'Abnormal cell morphology'),
(405937, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0100574', 'abnormal gastrula cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(405938, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0103104', 'abnormal zygote cortex morphology', 0.4444444444444444, 3.6715585125471644, 1.2774207542365574, 'UPHENO:0086172', 'abnormal cell'),
(405939, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0103067', 'abnormal paracrine cell morphology', 0.5294117647058824, 5.43643956286526, 1.696500828969256, 'HP:0025461', 'Abnormal cell morphology'),
(405940, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0115617', 'abnormally posterioralized primordial germ cell', 0.43902439024390244, 5.43643956286526, 1.5449043867452603, 'HP:0025461', 'Abnormal cell morphology'),
(405941, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0101004', 'abnormal acid secreting cell', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(405942, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0100285', 'abnormal progenitor cell', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(405943, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0100715', 'abnormal ciliated cell', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(405944, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0101713', 'abnormal anatomical entity in vitro morphology', 0.41379310344827586, 2.7446671847279203, 1.0657036887902793, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(405945, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0102819', 'abnormal dorsolateral commissural neuron morphology', 0.4186046511627907, 5.43643956286526, 1.5085486027240909, 'HP:0025461', 'Abnormal cell morphology'),
(405946, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0100515', 'abnormal somatic stem cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(405947, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0102081', 'abnormal lymphocyte morphology', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(405948, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0102153', 'abnormal animal blastomere morphology', 0.4186046511627907, 5.43643956286526, 1.5085486027240909, 'HP:0025461', 'Abnormal cell morphology'),
(405949, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0107341', 'abnormal neutrophil morphology', 0.44, 5.9590888072311134, 1.6192588042625211, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(405950, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0101770', 'abnormal trunk vasculature morphology', 0.4090909090909091, 5.9590888072311134, 1.5613484740773398, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(405951, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0102693', 'abnormal plasma membrane morphology', 0.45714285714285713, 3.6715585125471644, 1.2955411026258445, 'UPHENO:0086172', 'abnormal cell'),
(405952, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0102504', 'abnormal neuroendocrine cell morphology', 0.4186046511627907, 5.43643956286526, 1.5085486027240909, 'HP:0025461', 'Abnormal cell morphology'),
(405953, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0102539', 'abnormal cytoplasm morphology', 0.45714285714285713, 3.6715585125471644, 1.2955411026258445, 'UPHENO:0086172', 'abnormal cell'),
(405954, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0102915', 'abnormal left-ventral blastomere morphology', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(405955, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0101513', 'abnormal basal body', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(405956, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0139758', 'abnormally necrotic oocyte', 0.43902439024390244, 5.43643956286526, 1.5449043867452603, 'HP:0025461', 'Abnormal cell morphology'),
(405957, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0140781', 'abnormally necrotic stage I oocyte', 0.4090909090909091, 5.43643956286526, 1.491307481034791, 'HP:0025461', 'Abnormal cell morphology'),
(405958, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0142064', 'abnormal desmosome morphology', 0.45714285714285713, 3.6715585125471644, 1.2955411026258445, 'UPHENO:0086172', 'abnormal cell'),
(405959, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0102285', 'abnormal myoblast morphology', 0.5294117647058824, 5.43643956286526, 1.696500828969256, 'HP:0025461', 'Abnormal cell morphology'),
(405960, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0103099', 'abnormal alkali secreting cell morphology', 0.5294117647058824, 5.43643956286526, 1.696500828969256, 'HP:0025461', 'Abnormal cell morphology'),
(405961, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0141296', 'abnormal adherens junction morphology', 0.45714285714285713, 3.6715585125471644, 1.2955411026258445, 'UPHENO:0086172', 'abnormal cell'),
(405962, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0140903', 'abnormally necrotic endothelial cell', 0.4583333333333333, 5.9590888072311134, 1.652649096646833, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(405963, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0102625', 'abnormal ligament cell morphology', 0.4186046511627907, 5.43643956286526, 1.5085486027240909, 'HP:0025461', 'Abnormal cell morphology'),
(405964, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0102047', 'abnormal secretory epithelial cell morphology', 0.46153846153846156, 5.43643956286526, 1.5840220806831131, 'HP:0025461', 'Abnormal cell morphology'),
(405965, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0100108', 'abnormal cell part', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(405966, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0102998', 'abnormal morula cell morphology', 0.47368421052631576, 5.43643956286526, 1.6047291305419304, 'HP:0025461', 'Abnormal cell morphology'),
(405967, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0141030', 'abnormally necrotic cardiac progenitor cell', 0.44, 5.9590888072311134, 1.6192588042625211, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(405968, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0102534', 'abnormal spermatocyte morphology', 0.5, 5.43643956286526, 1.6487024538808177, 'HP:0025461', 'Abnormal cell morphology'),
(405969, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0129551', 'increased size of the cell part', 0.42105263157894735, 3.6715585125471644, 1.2433500608051093, 'UPHENO:0086172', 'abnormal cell'),
(405970, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0140010', 'abnormally necrotic zygote', 0.47368421052631576, 5.43643956286526, 1.6047291305419304, 'HP:0025461', 'Abnormal cell morphology'),
(405971, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0103080', 'abnormal myelin accumulating cell morphology', 0.5294117647058824, 5.43643956286526, 1.696500828969256, 'HP:0025461', 'Abnormal cell morphology'),
(405972, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0102030', 'abnormal vegetal blastomere morphology', 0.4186046511627907, 5.43643956286526, 1.5085486027240909, 'HP:0025461', 'Abnormal cell morphology'),
(405973, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0102258', 'abnormal primordial germ cell morphology', 0.5, 5.43643956286526, 1.6487024538808177, 'HP:0025461', 'Abnormal cell morphology'),
(405974, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0107412', 'abnormal adult thrombocyte morphology', 0.4782608695652174, 5.9590888072311134, 1.6881940038877956, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(405975, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0102935', 'abnormal bulbous arteriosis morphology', 0.45, 5.9590888072311134, 1.6375560946892784, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(405976, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0102621', 'abnormal right blastomere morphology', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(405977, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0101366', 'abnormal morula cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(405978, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0141023', 'abnormally necrotic ciliated non-epidermal cell', 0.43902439024390244, 5.43643956286526, 1.5449043867452603, 'HP:0025461', 'Abnormal cell morphology'),
(405979, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0139838', 'abnormally necrotic proepicardium', 0.43902439024390244, 5.43643956286526, 1.5449043867452603, 'HP:0025461', 'Abnormal cell morphology'),
(405980, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0133438', 'abnormal cilium morphology in the ciliated non-epidermal cell', 0.42105263157894735, 3.6715585125471644, 1.2433500608051093, 'UPHENO:0086172', 'abnormal cell'),
(405981, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0100026', 'abnormal germ cell', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(405982, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0103122', 'abnormal ectodermal cell morphology', 0.4090909090909091, 5.43643956286526, 1.491307481034791, 'HP:0025461', 'Abnormal cell morphology'),
(405983, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0139839', 'abnormally necrotic progenitor cell', 0.47368421052631576, 5.43643956286526, 1.6047291305419304, 'HP:0025461', 'Abnormal cell morphology'),
(405984, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0101113', 'abnormal stage IV oocyte', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(405985, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0103021', 'abnormal wedge region morphology', 0.43243243243243246, 3.6715585125471644, 1.2600400701560144, 'UPHENO:0086172', 'abnormal cell'),
(405986, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0141154', 'abnormally necrotic barrier cell', 0.47368421052631576, 5.43643956286526, 1.6047291305419304, 'HP:0025461', 'Abnormal cell morphology'),
(405987, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0100004', 'abnormal cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(405988, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0100176', 'abnormal stage VI oocyte', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(405989, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0140393', 'abnormally necrotic spermatocyte', 0.43902439024390244, 5.43643956286526, 1.5449043867452603, 'HP:0025461', 'Abnormal cell morphology'),
(405990, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0102333', 'abnormal microglial cell morphology', 0.4186046511627907, 5.43643956286526, 1.5085486027240909, 'HP:0025461', 'Abnormal cell morphology'),
(405991, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0101241', 'abnormal nucleate erythrocyte', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(405992, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0101897', 'abnormal sensory epithelial cell morphology', 0.46153846153846156, 5.43643956286526, 1.5840220806831131, 'HP:0025461', 'Abnormal cell morphology'),
(405993, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0101461', 'abnormal sperm entry point', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(405994, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0100917', 'abnormal stage III oocyte', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(405995, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0139717', 'abnormally necrotic cell', 0.5142857142857142, 5.43643956286526, 1.6720894724144628, 'HP:0025461', 'Abnormal cell morphology'),
(405996, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0101968', 'abnormal interneuron morphology', 0.4090909090909091, 5.43643956286526, 1.491307481034791, 'HP:0025461', 'Abnormal cell morphology'),
(405997, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0103167', 'abnormal absorptive cell morphology', 0.5294117647058824, 5.43643956286526, 1.696500828969256, 'HP:0025461', 'Abnormal cell morphology'),
(405998, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0101326', 'abnormal cementoblast', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(405999, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0140973', 'abnormally necrotic erythroid cell', 0.4090909090909091, 5.43643956286526, 1.491307481034791, 'HP:0025461', 'Abnormal cell morphology'),
(406000, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0102871', 'abnormal olfactory epithelial support cell morphology', 0.4090909090909091, 5.43643956286526, 1.491307481034791, 'HP:0025461', 'Abnormal cell morphology'),
(406001, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0102852', 'abnormal centriole morphology', 0.4444444444444444, 3.6715585125471644, 1.2774207542365574, 'UPHENO:0086172', 'abnormal cell'),
(406002, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0103150', 'abnormal B cell morphology', 0.42857142857142855, 5.43643956286526, 1.526401870347189, 'HP:0025461', 'Abnormal cell morphology'),
(406003, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0102532', 'abnormal angioblast morphology', 0.5789473684210527, 5.9590888072311134, 1.8574172345312732, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(406004, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0102147', 'abnormal somatic stem cell morphology', 0.5, 5.43643956286526, 1.6487024538808177, 'HP:0025461', 'Abnormal cell morphology'),
(406005, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0103129', 'abnormal ciliary axoneme morphology', 0.43243243243243246, 3.6715585125471644, 1.2600400701560144, 'UPHENO:0086172', 'abnormal cell'),
(406006, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0101498', 'abnormal stage II oocyte', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(406007, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0142067', 'abnormally necrotic desmosome', 0.42105263157894735, 3.6715585125471644, 1.2433500608051093, 'UPHENO:0086172', 'abnormal cell'),
(406008, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0102024', 'abnormal cilium morphology', 0.4444444444444444, 3.6715585125471644, 1.2774207542365574, 'UPHENO:0086172', 'abnormal cell'),
(406009, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0140899', 'abnormally necrotic mucus secreting cell', 0.47368421052631576, 5.43643956286526, 1.6047291305419304, 'HP:0025461', 'Abnormal cell morphology'),
(406010, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0141503', 'abnormal lymphoblast morphology', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(406011, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0102794', 'abnormal stromal cell morphology', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(406012, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0102109', 'abnormal pericyte morphology', 0.5294117647058824, 5.43643956286526, 1.696500828969256, 'HP:0025461', 'Abnormal cell morphology'),
(406013, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0102765', 'abnormal motor neuron morphology', 0.4186046511627907, 5.43643956286526, 1.5085486027240909, 'HP:0025461', 'Abnormal cell morphology'),
(406014, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0102061', 'abnormal spermatid morphology', 0.5, 5.43643956286526, 1.6487024538808177, 'HP:0025461', 'Abnormal cell morphology'),
(406015, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0100477', 'abnormal pericyte', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(406016, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0141478', 'abnormally necrotic lymphoblast', 0.4090909090909091, 5.43643956286526, 1.491307481034791, 'HP:0025461', 'Abnormal cell morphology'),
(406017, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0100791', 'abnormal multiciliated cell precursor', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(406018, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0115704', 'abnormally defasciculated motor neuron', 0.4090909090909091, 5.43643956286526, 1.491307481034791, 'HP:0025461', 'Abnormal cell morphology'),
(406019, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0102323', 'abnormal keratin accumulating cell morphology', 0.5294117647058824, 5.43643956286526, 1.696500828969256, 'HP:0025461', 'Abnormal cell morphology'),
(406020, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0128761', 'decreased size of the angioblast', 0.44, 5.9590888072311134, 1.6192588042625211, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(406021, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0100653', 'abnormal myoblast', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(406022, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0128071', 'decreased size of the cell part', 0.42105263157894735, 3.6715585125471644, 1.2433500608051093, 'UPHENO:0086172', 'abnormal cell'),
(406023, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0100626', 'abnormal primordial germ cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(406024, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0102494', 'abnormal blastomere V1 morphology', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(406025, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0129486', 'increased size of the cell', 0.4186046511627907, 5.43643956286526, 1.5085486027240909, 'HP:0025461', 'Abnormal cell morphology'),
(406026, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0101547', 'abnormal lampbrush chromosome', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(406027, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0102474', 'abnormal left-dorsal blastomere morphology', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(406028, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0140068', 'abnormally necrotic myoblast', 0.47368421052631576, 5.43643956286526, 1.6047291305419304, 'HP:0025461', 'Abnormal cell morphology'),
(406029, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0140803', 'abnormally necrotic pericyte', 0.47368421052631576, 5.43643956286526, 1.6047291305419304, 'HP:0025461', 'Abnormal cell morphology'),
(406030, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0102113', 'abnormal anatomical line morphology', 0.41379310344827586, 2.7446671847279203, 1.0657036887902793, 'UPHENO:0020584', 'abnormal anatomical entity morphology'),
(406031, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0115758', 'abnormally decreased mobility of melanoblast', 0.42424242424242425, 3.6715585125471644, 1.2480508339450433, 'UPHENO:0086172', 'abnormal cell'),
(406032, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0140287', 'abnormally necrotic epicardial precursor cell', 0.42857142857142855, 7.414388317771038, 1.7825809920815505, 'UPHENO:0076810', 'abnormal heart morphology'),
(406033, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0130239', 'increased size of the angioblast', 0.44, 5.9590888072311134, 1.6192588042625211, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(406034, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0102526', 'abnormal nucleus morphology', 0.45714285714285713, 3.6715585125471644, 1.2955411026258445, 'UPHENO:0086172', 'abnormal cell'),
(406035, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0102872', 'abnormal ciliated non-epidermal cell morphology', 0.5, 5.43643956286526, 1.6487024538808177, 'HP:0025461', 'Abnormal cell morphology'),
(406036, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0140429', 'abnormally necrotic hemangioblast', 0.4090909090909091, 5.43643956286526, 1.491307481034791, 'HP:0025461', 'Abnormal cell morphology'),
(406037, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0141203', 'abnormally necrotic exocrine cell', 0.47368421052631576, 5.43643956286526, 1.6047291305419304, 'HP:0025461', 'Abnormal cell morphology'),
(406038, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0101472', 'abnormal zygote cortex', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(406039, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0101480', 'abnormal stage V oocyte', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(406040, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0101409', 'abnormal perivitelline space', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(406041, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0102896', 'abnormal mitotic spindle morphology', 0.45714285714285713, 3.6715585125471644, 1.2955411026258445, 'UPHENO:0086172', 'abnormal cell'),
(406042, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0102800', 'abnormal circulating cell morphology', 0.5789473684210527, 5.9590888072311134, 1.8574172345312732, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(406043, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0103130', 'abnormal stage II oocyte morphology', 0.47368421052631576, 5.43643956286526, 1.6047291305419304, 'HP:0025461', 'Abnormal cell morphology'),
(406044, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0102848', 'abnormal macrophage morphology', 0.44, 5.9590888072311134, 1.6192588042625211, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(406045, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0139951', 'abnormally necrotic lymphocyte', 0.4090909090909091, 5.43643956286526, 1.491307481034791, 'HP:0025461', 'Abnormal cell morphology'),
(406046, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0101228', 'abnormal mesenchymal stem cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(406047, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0107410', 'abnormal thrombocyte morphology', 0.5, 5.9590888072311134, 1.7261356851694936, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(406048, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0140868', 'abnormally necrotic chondroblast', 0.47368421052631576, 5.43643956286526, 1.6047291305419304, 'HP:0025461', 'Abnormal cell morphology'),
(406049, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0140533', 'abnormally necrotic myelin accumulating cell', 0.47368421052631576, 5.43643956286526, 1.6047291305419304, 'HP:0025461', 'Abnormal cell morphology'),
(406050, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0102434', 'abnormal exocrine cell morphology', 0.5294117647058824, 5.43643956286526, 1.696500828969256, 'HP:0025461', 'Abnormal cell morphology'),
(406051, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0128027', 'decreased size of the circulating cell', 0.44, 5.9590888072311134, 1.6192588042625211, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(406052, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0140451', 'abnormally necrotic sensory epithelial cell', 0.4090909090909091, 5.43643956286526, 1.491307481034791, 'HP:0025461', 'Abnormal cell morphology'),
(406053, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0142057', 'abnormal desmosome', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(406054, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0140075', 'abnormally necrotic stem cell', 0.47368421052631576, 5.43643956286526, 1.6047291305419304, 'HP:0025461', 'Abnormal cell morphology'),
(406055, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0102416', 'abnormal left blastomere morphology', 0.45, 5.43643956286526, 1.5640964814516294, 'HP:0025461', 'Abnormal cell morphology'),
(406056, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0140267', 'abnormally necrotic multiciliated cell', 0.43902439024390244, 5.43643956286526, 1.5449043867452603, 'HP:0025461', 'Abnormal cell morphology'),
(406057, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0141147', 'abnormally necrotic alkali secreting cell', 0.47368421052631576, 5.43643956286526, 1.6047291305419304, 'HP:0025461', 'Abnormal cell morphology'),
(406058, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0102446', 'abnormal natural killer cell morphology', 0.4090909090909091, 5.43643956286526, 1.491307481034791, 'HP:0025461', 'Abnormal cell morphology'),
(406059, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0141277', 'abnormal actin cytoskeleton morphology', 0.45714285714285713, 3.6715585125471644, 1.2955411026258445, 'UPHENO:0086172', 'abnormal cell'),
(406060, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0141007', 'abnormally necrotic electrically active cell', 0.47368421052631576, 5.43643956286526, 1.6047291305419304, 'HP:0025461', 'Abnormal cell morphology'),
(406061, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0100691', 'abnormal keratin accumulating cell', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(406062, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0102808', 'abnormal non-ciliated epithelial cell morphology', 0.46153846153846156, 5.43643956286526, 1.5840220806831131, 'HP:0025461', 'Abnormal cell morphology'),
(406063, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0107374', 'abnormal afferent neuron morphology', 0.4090909090909091, 5.43643956286526, 1.491307481034791, 'HP:0025461', 'Abnormal cell morphology'),
(406064, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0100307', 'abnormal blastomere', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(406065, 'HP:0031331', 'Abnormal cardiomyocyte morphology', 'XPO:0101939', 'abnormal blastomere morphology', 0.47368421052631576, 5.43643956286526, 1.6047291305419304, 'HP:0025461', 'Abnormal cell morphology'),
(406066, 'HP:0012561', 'Unicuspid aortic valve', 'XPO:0102877', 'abnormal ventricular outflow tract morphology', 0.40625, 9.40147820888365, 1.9543158706716228, 'UPHENO:0086866', 'abnormal cardiac ventricle morphology'),
(406067, 'HP:0012561', 'Unicuspid aortic valve', 'XPO:0102769', 'abnormal cardiac valve morphology', 0.4126984126984127, 10.21769640676594, 2.053491438625099, 'UPHENO:0015319', 'abnormal cardiac valve morphology in the heart'),
(406068, 'HP:0012561', 'Unicuspid aortic valve', 'XPO:0102368', 'abnormal cardiac ventricle morphology', 0.40625, 9.40147820888365, 1.9543158706716228, 'UPHENO:0086866', 'abnormal cardiac ventricle morphology'),
(406069, 'HP:0010356', 'Abnormality of the distal phalanx of the 2nd toe', 'XPO:0102180', 'abnormal hindlimb digit 3 morphology', 0.4111111111111111, 7.639349617137506, 1.7721798749753483, 'HP:0001780', 'Abnormal toe morphology'),
(406070, 'HP:0010356', 'Abnormality of the distal phalanx of the 2nd toe', 'XPO:0100178', 'abnormal digit', 0.4444444444444444, 6.393467666143939, 1.6856871551248356, 'HP:0011297', 'Abnormal digit morphology'),
(406071, 'HP:0010356', 'Abnormality of the distal phalanx of the 2nd toe', 'XPO:0102876', 'abnormal hindlimb digit 4 morphology', 0.4111111111111111, 7.639349617137506, 1.7721798749753483, 'UPHENO:0088132', 'abnormal pedal digit morphology'),
(406072, 'HP:0010356', 'Abnormality of the distal phalanx of the 2nd toe', 'XPO:0102948', 'abnormal hindlimb digit 5 morphology', 0.4111111111111111, 7.639349617137506, 1.7721798749753483, 'HP:0001780', 'Abnormal toe morphology'),
(406073, 'HP:0010356', 'Abnormality of the distal phalanx of the 2nd toe', 'XPO:0101248', 'abnormal digit-joint region', 0.42424242424242425, 6.393467666143939, 1.6469305455909364, 'UPHENO:0002905', 'abnormal digit'),
(406074, 'HP:0010356', 'Abnormality of the distal phalanx of the 2nd toe', 'XPO:0102051', 'abnormal hindlimb digit 2 morphology', 0.4111111111111111, 7.639349617137506, 1.7721798749753483, 'UPHENO:0088132', 'abnormal pedal digit morphology'),
(406075, 'HP:0010356', 'Abnormality of the distal phalanx of the 2nd toe', 'XPO:0103627', 'abnormally increased number of hindlimb digit', 0.41935483870967744, 7.639349617137506, 1.7898598343282457, 'HP:0001780', 'Abnormal toe morphology'),
(406076, 'HP:0010356', 'Abnormality of the distal phalanx of the 2nd toe', 'XPO:0102880', 'abnormal digit-joint region morphology', 0.410958904109589, 6.466375519622663, 1.630157844230185, 'UPHENO:0086700', 'abnormal digit morphology'),
(406077, 'HP:0010356', 'Abnormality of the distal phalanx of the 2nd toe', 'XPO:0101810', 'abnormal digit morphology', 0.410958904109589, 6.466375519622663, 1.630157844230185, 'UPHENO:0086700', 'abnormal digit morphology'),
(406078, 'HP:0010356', 'Abnormality of the distal phalanx of the 2nd toe', 'XPO:0101872', 'abnormal hindlimb digit 1 morphology', 0.4111111111111111, 7.639349617137506, 1.7721798749753483, 'UPHENO:0088132', 'abnormal pedal digit morphology'),
(406079, 'HP:0010356', 'Abnormality of the distal phalanx of the 2nd toe', 'XPO:0139979', 'abnormally necrotic claw primordium', 0.40217391304347827, 7.639349617137506, 1.7528112073555977, 'HP:0001780', 'Abnormal toe morphology'),
(406080, 'HP:0010356', 'Abnormality of the distal phalanx of the 2nd toe', 'XPO:0101809', 'abnormal hindlimb digit morphology', 0.42045454545454547, 7.639349617137506, 1.792205141952758, 'HP:0001780', 'Abnormal toe morphology'),
(406081, 'HP:0010356', 'Abnormality of the distal phalanx of the 2nd toe', 'XPO:0102566', 'abnormal claw primordium morphology', 0.42528735632183906, 7.639349617137506, 1.8024757426081115, 'HP:0001780', 'Abnormal toe morphology'),
(406082, 'HP:3000011', 'Abnormality of palatoglossus muscle', 'XPO:0128105', 'decreased size of the tongue', 0.4470588235294118, 11.945263302929897, 2.310894925987959, 'HP:0030809', 'Abnormal tongue morphology'),
(406083, 'HP:3000011', 'Abnormality of palatoglossus muscle', 'XPO:0103352', 'decreased size of the mouth', 0.4166666666666667, 7.884497199543557, 1.812514045870123, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(406084, 'HP:3000011', 'Abnormality of palatoglossus muscle', 'XPO:0103199', 'abnormal tongue morphology', 0.5068493150684932, 10.93592543835056, 2.354329271378176, 'HP:0000157', 'Abnormality of the tongue'),
(406085, 'HP:3000011', 'Abnormality of palatoglossus muscle', 'XPO:0127750', 'abnormally localised tongue', 0.45454545454545453, 10.93592543835056, 2.2295459625785368, 'HP:0000157', 'Abnormality of the tongue'),
(406086, 'HP:3000011', 'Abnormality of palatoglossus muscle', 'XPO:0101567', 'abnormal tongue', 0.5074626865671642, 10.93592543835056, 2.355753404548865, 'HP:0000157', 'Abnormality of the tongue'),
(406087, 'HP:3000011', 'Abnormality of palatoglossus muscle', 'XPO:0102279', 'abnormal mouth morphology', 0.44, 7.312692920701687, 1.7937627728071353, 'UPHENO:0076800', 'abnormal mouth morphology'),
(406088, 'HP:3000011', 'Abnormality of palatoglossus muscle', 'XPO:0103138', 'abnormal upper jaw morphology', 0.42045454545454547, 8.81758714901448, 1.9254595806572323, 'UPHENO:0087585', 'abnormal midface morphology'),
(406089, 'HP:3000011', 'Abnormality of palatoglossus muscle', 'XPO:0126089', 'absent tongue', 0.4430379746835443, 10.93592543835056, 2.201142943449399, 'HP:0000157', 'Abnormality of the tongue'),
(406090, 'HP:3000011', 'Abnormality of palatoglossus muscle', 'XPO:0115558', 'abnormally incomplete structure of mouth', 0.4342105263157895, 7.312692920701687, 1.7819226251113227, 'UPHENO:0076800', 'abnormal mouth morphology'),
(406091, 'HP:3000011', 'Abnormality of palatoglossus muscle', 'XPO:0140626', 'abnormally necrotic tongue', 0.47435897435897434, 10.93592543835056, 2.277620331530738, 'HP:0000157', 'Abnormality of the tongue'),
(406092, 'HP:3000011', 'Abnormality of palatoglossus muscle', 'XPO:0103735', 'increased size of the mouth', 0.4166666666666667, 7.884497199543557, 1.812514045870123, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(406093, 'HP:3000011', 'Abnormality of palatoglossus muscle', 'XPO:0130628', 'increased size of the oral cavity', 0.4375, 7.884497199543557, 1.8572742190641387, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(406094, 'HP:3000011', 'Abnormality of palatoglossus muscle', 'XPO:0141311', 'abnormal roof of mouth morphology', 0.4230769230769231, 7.312692920701687, 1.7589291117884391, 'UPHENO:0076800', 'abnormal mouth morphology'),
(406095, 'HP:3000011', 'Abnormality of palatoglossus muscle', 'XPO:0129152', 'decreased size of the oral cavity', 0.4375, 7.884497199543557, 1.8572742190641387, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(406096, 'HP:3000011', 'Abnormality of palatoglossus muscle', 'XPO:0115393', 'abnormally decreased volume of oral cavity', 0.4268292682926829, 7.884497199543557, 1.8344847152639032, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(406097, 'HP:3000011', 'Abnormality of palatoglossus muscle', 'XPO:0103096', 'abnormal oral cavity morphology', 0.4666666666666667, 7.884497199543557, 1.9181845652735452, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(406098, 'HP:3000011', 'Abnormality of palatoglossus muscle', 'XPO:0129585', 'increased size of the tongue', 0.5058823529411764, 11.945263302929897, 2.458230645441567, 'HP:0030809', 'Abnormal tongue morphology'),
(406099, 'HP:0011115', 'Abnormal circulating chemokine concentration', 'XPO:0141911', 'abnormal ribose phosphate metabolic process', 0.40540540540540543, 7.272470629310105, 1.7170611240647105, 'UPHENO:0050113', 'abnormal cellular metabolic process'),
(406100, 'HP:0011115', 'Abnormal circulating chemokine concentration', 'XPO:0141877', 'abnormal 2-deoxyribose 1-phosphate metabolic process', 0.40540540540540543, 7.272470629310105, 1.7170611240647105, 'UPHENO:0050113', 'abnormal cellular metabolic process'),
(406101, 'HP:0011115', 'Abnormal circulating chemokine concentration', 'XPO:0141790', 'abnormal cellular metabolic process', 0.42857142857142855, 7.272470629310105, 1.7654385083732562, 'UPHENO:0050113', 'abnormal cellular metabolic process'),
(406102, 'HP:0006562', 'Viral hepatitis', 'XPO:0100042', 'abnormal hepatic vein', 0.40229885057471265, 10.01729298920255, 2.0074724046487695, 'UPHENO:0019492', 'abnormal liver morphology'),
(406103, 'HP:0034275', 'Verrucous epidermal nevus', 'XPO:0102561', 'abnormal dermis morphology', 0.42857142857142855, 7.420886955069779, 1.7833620281931915, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(406104, 'HP:0034275', 'Verrucous epidermal nevus', 'XPO:0102886', 'abnormal stratum compactum morphology', 0.4090909090909091, 7.420886955069779, 1.7423597190908553, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(406105, 'HP:0034275', 'Verrucous epidermal nevus', 'XPO:0100983', 'abnormal skin gland', 0.45454545454545453, 6.8660902472206855, 1.7666211003984522, 'HP:0000951', 'Abnormality of the skin'),
(406106, 'HP:0034275', 'Verrucous epidermal nevus', 'XPO:0102615', 'abnormal skin gland morphology', 0.43902439024390244, 7.420886955069779, 1.8049793268950312, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(406107, 'HP:0034275', 'Verrucous epidermal nevus', 'XPO:0101322', 'abnormal iridophore', 0.40540540540540543, 6.8660902472206855, 1.6683974647021622, 'HP:0000951', 'Abnormality of the skin'),
(406108, 'HP:0034275', 'Verrucous epidermal nevus', 'XPO:0101254', 'abnormal stratum compactum', 0.4166666666666667, 6.8660902472206855, 1.6914109306558096, 'HP:0000951', 'Abnormality of the skin'),
(406109, 'HP:0034275', 'Verrucous epidermal nevus', 'XPO:0102910', 'abnormal pigment cell morphology', 0.4090909090909091, 7.420886955069779, 1.7423597190908553, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(406110, 'HP:0034275', 'Verrucous epidermal nevus', 'XPO:0100929', 'abnormal dermis', 0.4411764705882353, 6.8660902472206855, 1.740447489012273, 'HP:0000951', 'Abnormality of the skin'),
(406111, 'HP:0034275', 'Verrucous epidermal nevus', 'XPO:0102176', 'abnormal neuromast support cell morphology', 0.4090909090909091, 7.420886955069779, 1.7423597190908553, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(406112, 'HP:0034275', 'Verrucous epidermal nevus', 'XPO:0101208', 'abnormal stratum spongiosum', 0.4166666666666667, 6.8660902472206855, 1.6914109306558096, 'HP:0000951', 'Abnormality of the skin'),
(406113, 'HP:0034275', 'Verrucous epidermal nevus', 'XPO:0101278', 'abnormal pigment cell', 0.4166666666666667, 6.8660902472206855, 1.6914109306558096, 'HP:0000951', 'Abnormality of the skin'),
(406114, 'HP:0034275', 'Verrucous epidermal nevus', 'XPO:0101313', 'abnormal Eberth-Kastschenko layer', 0.4166666666666667, 6.8660902472206855, 1.6914109306558096, 'HP:0000951', 'Abnormality of the skin'),
(406115, 'HP:0034275', 'Verrucous epidermal nevus', 'XPO:0101095', 'abnormal skin seromucous gland', 0.4411764705882353, 6.8660902472206855, 1.740447489012273, 'HP:0000951', 'Abnormality of the skin'),
(406116, 'HP:0034275', 'Verrucous epidermal nevus', 'XPO:0102139', 'abnormal skin morphology', 0.43902439024390244, 7.420886955069779, 1.8049793268950312, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(406117, 'HP:0034275', 'Verrucous epidermal nevus', 'XPO:0100544', 'abnormal neuromast support cell', 0.4166666666666667, 6.8660902472206855, 1.6914109306558096, 'HP:0000951', 'Abnormality of the skin'),
(406118, 'HP:0034275', 'Verrucous epidermal nevus', 'XPO:0101515', 'abnormal neuromast mantle cell', 0.4166666666666667, 6.8660902472206855, 1.6914109306558096, 'HP:0000951', 'Abnormality of the skin'),
(406119, 'HP:0034275', 'Verrucous epidermal nevus', 'XPO:0100507', 'abnormal skin', 0.46875, 6.8660902472206855, 1.7940122082596586, 'HP:0000951', 'Abnormality of the skin'),
(406120, 'HP:0034275', 'Verrucous epidermal nevus', 'XPO:0102626', 'abnormal granular gland morphology', 0.4186046511627907, 7.420886955069779, 1.7625032752155354, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(406121, 'HP:0034275', 'Verrucous epidermal nevus', 'XPO:0100994', 'abnormal granular gland', 0.4411764705882353, 6.8660902472206855, 1.740447489012273, 'HP:0000951', 'Abnormality of the skin'),
(406122, 'HP:0034275', 'Verrucous epidermal nevus', 'XPO:0102945', 'abnormal Eberth-Kastschenko layer morphology', 0.4090909090909091, 7.420886955069779, 1.7423597190908553, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(406123, 'HP:0034275', 'Verrucous epidermal nevus', 'XPO:0103147', 'abnormal neuromast mantle cell morphology', 0.4090909090909091, 7.420886955069779, 1.7423597190908553, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(406124, 'HP:0034275', 'Verrucous epidermal nevus', 'XPO:0101387', 'abnormal melanophore', 0.40540540540540543, 6.8660902472206855, 1.6683974647021622, 'HP:0000951', 'Abnormality of the skin'),
(406125, 'HP:0034275', 'Verrucous epidermal nevus', 'XPO:0101529', 'abnormal skin mucous gland', 0.4166666666666667, 6.8660902472206855, 1.6914109306558096, 'HP:0000951', 'Abnormality of the skin'),
(406126, 'HP:0034275', 'Verrucous epidermal nevus', 'XPO:0101591', 'abnormal xanthophore', 0.40540540540540543, 6.8660902472206855, 1.6683974647021622, 'HP:0000951', 'Abnormality of the skin'),
(406127, 'HP:0034275', 'Verrucous epidermal nevus', 'XPO:0102727', 'abnormal skin seromucous gland morphology', 0.4186046511627907, 7.420886955069779, 1.7625032752155354, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(406128, 'HP:0034275', 'Verrucous epidermal nevus', 'XPO:0102840', 'abnormal stratum spongiosum morphology', 0.4090909090909091, 7.420886955069779, 1.7423597190908553, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(406129, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0140029', 'abnormally necrotic basal forebrain', 0.4264705882352941, 8.02346099791745, 1.8498027277157947, 'HP:0002060', 'Abnormal cerebral morphology'),
(406130, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0140330', 'abnormally necrotic dorsal pallidum', 0.4027777777777778, 8.02346099791745, 1.7976851200440698, 'HP:0002060', 'Abnormal cerebral morphology'),
(406131, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0101664', 'abnormal nervous system morphology', 0.4222222222222222, 4.7814666189787065, 1.4208594094232423, 'HP:0012639', 'Abnormal nervous system morphology'),
(406132, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0103057', 'abnormal medial amygdala morphology', 0.4264705882352941, 8.02346099791745, 1.8498027277157947, 'HP:0002060', 'Abnormal cerebral morphology'),
(406133, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0101140', 'abnormal ventrolateral thalamic nucleus', 0.43548387096774194, 6.667568321314008, 1.704000722566664, 'HP:0100547', 'Abnormal forebrain morphology'),
(406134, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0102357', 'abnormal subpallium morphology', 0.4603174603174603, 8.02346099791745, 1.9218062310018553, 'HP:0002060', 'Abnormal cerebral morphology'),
(406135, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0102200', 'abnormal telencephalon septum morphology', 0.43283582089552236, 8.02346099791745, 1.8635560972122107, 'HP:0002060', 'Abnormal cerebral morphology'),
(406136, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0100695', 'abnormal zona limitans intrathalamica', 0.45, 6.667568321314008, 1.7321679319833003, 'HP:0100547', 'Abnormal forebrain morphology'),
(406137, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0107340', 'abnormal enteric nervous system morphology', 0.40425531914893614, 4.7814666189787065, 1.3902997209433732, 'HP:0012639', 'Abnormal nervous system morphology'),
(406138, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0140574', 'abnormally necrotic medial ganglionic eminence', 0.4142857142857143, 8.02346099791745, 1.8231854734408677, 'HP:0002060', 'Abnormal cerebral morphology'),
(406139, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0101970', 'abnormal lateral ganglionic eminence morphology', 0.4461538461538462, 8.02346099791745, 1.8920089808682852, 'HP:0002060', 'Abnormal cerebral morphology'),
(406140, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0101106', 'abnormal caudal tuberal region', 0.43548387096774194, 6.667568321314008, 1.704000722566664, 'HP:0100547', 'Abnormal forebrain morphology'),
(406141, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0115310', 'abnormally incomplete structure of forebrain', 0.43548387096774194, 6.667568321314008, 1.704000722566664, 'HP:0100547', 'Abnormal forebrain morphology'),
(406142, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0100998', 'abnormal rostral tuberal region', 0.43548387096774194, 6.667568321314008, 1.704000722566664, 'HP:0100547', 'Abnormal forebrain morphology'),
(406143, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0130244', 'increased size of the dorsal pallium', 0.4084507042253521, 8.02346099791745, 1.810300608993995, 'HP:0002060', 'Abnormal cerebral morphology'),
(406144, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0126877', 'abnormally localised diencephalon', 0.4090909090909091, 6.667568321314008, 1.6515573214369805, 'HP:0100547', 'Abnormal forebrain morphology'),
(406145, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0101795', 'abnormal central amygdala morphology', 0.44155844155844154, 10.854497839006713, 2.1892681767410944, 'HP:0034221', 'Abnormal temporal lobe morphology'),
(406146, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0102066', 'abnormal ventral pallium morphology', 0.453125, 8.02346099791745, 1.9067330082319718, 'HP:0002060', 'Abnormal cerebral morphology'),
(406147, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0102633', 'abnormal ventricular zone morphology', 0.4067796610169492, 6.005340694266148, 1.562962076284922, 'UPHENO:0081435', 'abnormal anatomical entity morphology in the brain'),
(406148, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0129667', 'increased size of the basal ganglion', 0.4027777777777778, 8.02346099791745, 1.7976851200440698, 'HP:0002060', 'Abnormal cerebral morphology'),
(406149, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0102131', 'abnormal glomerular layer of the olfactory bulb morphology', 0.42857142857142855, 8.651717009412357, 1.9255852924032166, 'UPHENO:0087531', 'abnormal cerebral hemisphere morphology'),
(406150, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0130082', 'increased size of the subpallium', 0.4142857142857143, 8.02346099791745, 1.8231854734408677, 'HP:0002060', 'Abnormal cerebral morphology'),
(406151, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0102174', 'abnormal pallium morphology', 0.4603174603174603, 8.02346099791745, 1.9218062310018553, 'HP:0002060', 'Abnormal cerebral morphology'),
(406152, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0100729', 'abnormal thalamus', 0.4576271186440678, 6.667568321314008, 1.7467856420423753, 'HP:0100547', 'Abnormal forebrain morphology'),
(406153, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0101184', 'abnormal suprachiasmatic nucleus', 0.42857142857142855, 6.667568321314008, 1.6904228111816126, 'HP:0100547', 'Abnormal forebrain morphology'),
(406154, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0101420', 'abnormal magnocellular preoptic nucleus', 0.421875, 6.667568321314008, 1.677164388351466, 'HP:0100547', 'Abnormal forebrain morphology'),
(406155, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0127340', 'abnormally localised hypothalamus', 0.40298507462686567, 6.667568321314008, 1.639185931352649, 'HP:0100547', 'Abnormal forebrain morphology'),
(406156, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0101796', 'abnormal neural nucleus morphology', 0.4375, 5.483278994082134, 1.5488494310006167, 'HP:0002011', 'Morphological central nervous system abnormality'),
(406157, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0101123', 'abnormal third ventricle', 0.4426229508196721, 6.667568321314008, 1.7179111633526845, 'HP:0100547', 'Abnormal forebrain morphology'),
(406158, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0139879', 'abnormally necrotic telencephalon', 0.43283582089552236, 8.02346099791745, 1.8635560972122107, 'HP:0002060', 'Abnormal cerebral morphology'),
(406159, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0102854', 'abnormal medial septum morphology', 0.4264705882352941, 8.02346099791745, 1.8498027277157947, 'HP:0002060', 'Abnormal cerebral morphology'),
(406160, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0139760', 'abnormally necrotic basal ganglion', 0.4142857142857143, 8.02346099791745, 1.8231854734408677, 'HP:0002060', 'Abnormal cerebral morphology'),
(406161, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0140544', 'abnormally necrotic forebrain', 0.4090909090909091, 6.667568321314008, 1.6515573214369805, 'HP:0100547', 'Abnormal forebrain morphology'),
(406162, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0101805', 'abnormal pallidum morphology', 0.4393939393939394, 8.02346099791745, 1.8776208710622537, 'HP:0002060', 'Abnormal cerebral morphology'),
(406163, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0102238', 'abnormal basal forebrain morphology', 0.4603174603174603, 8.02346099791745, 1.9218062310018553, 'HP:0002060', 'Abnormal cerebral morphology'),
(406164, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0101652', 'abnormal external plexiform layer of the olfactory bulb morphology', 0.42857142857142855, 8.651717009412357, 1.9255852924032166, 'UPHENO:0087531', 'abnormal cerebral hemisphere morphology'),
(406165, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0101986', 'abnormal amygdala morphology', 0.4461538461538462, 8.02346099791745, 1.8920089808682852, 'HP:0002060', 'Abnormal cerebral morphology'),
(406166, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0100611', 'abnormal hypophysis', 0.4426229508196721, 6.667568321314008, 1.7179111633526845, 'HP:0100547', 'Abnormal forebrain morphology'),
(406167, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0101354', 'abnormal eminentia thalami', 0.4576271186440678, 6.667568321314008, 1.7467856420423753, 'HP:0100547', 'Abnormal forebrain morphology'),
(406168, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0100157', 'abnormal optic tract', 0.4576271186440678, 6.667568321314008, 1.7467856420423753, 'HP:0100547', 'Abnormal forebrain morphology'),
(406169, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0101588', 'abnormal central nucleus of the thalamus', 0.43548387096774194, 6.667568321314008, 1.704000722566664, 'HP:0100547', 'Abnormal forebrain morphology'),
(406170, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0128444', 'decreased size of the telencephalon', 0.42028985507246375, 8.02346099791745, 1.8363494384224073, 'HP:0002060', 'Abnormal cerebral morphology'),
(406171, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0100914', 'abnormal pars intermedia', 0.42857142857142855, 6.667568321314008, 1.6904228111816126, 'HP:0100547', 'Abnormal forebrain morphology'),
(406172, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0130557', 'increased size of the medial ganglionic eminence', 0.4027777777777778, 8.02346099791745, 1.7976851200440698, 'HP:0002060', 'Abnormal cerebral morphology'),
(406173, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0140854', 'abnormally necrotic ventral pallium', 0.42028985507246375, 8.02346099791745, 1.8363494384224073, 'HP:0002060', 'Abnormal cerebral morphology'),
(406174, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0101284', 'abnormal ventromedial thalamic nucleus', 0.43548387096774194, 6.667568321314008, 1.704000722566664, 'HP:0100547', 'Abnormal forebrain morphology'),
(406175, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0101293', 'abnormal posterior hypothalamus', 0.45, 6.667568321314008, 1.7321679319833003, 'HP:0100547', 'Abnormal forebrain morphology'),
(406176, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0101895', 'abnormal prethalamus morphology', 0.40298507462686567, 6.667568321314008, 1.639185931352649, 'HP:0100547', 'Abnormal forebrain morphology'),
(406177, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0100971', 'abnormal prethalamus basal plate', 0.43548387096774194, 6.667568321314008, 1.704000722566664, 'HP:0100547', 'Abnormal forebrain morphology'),
(406178, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0129924', 'increased size of the telencephalon', 0.42028985507246375, 8.02346099791745, 1.8363494384224073, 'HP:0002060', 'Abnormal cerebral morphology'),
(406179, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0140186', 'abnormally necrotic pallium', 0.4264705882352941, 8.02346099791745, 1.8498027277157947, 'HP:0002060', 'Abnormal cerebral morphology'),
(406180, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0100951', 'abnormal adenohypophysis', 0.43548387096774194, 6.667568321314008, 1.704000722566664, 'HP:0100547', 'Abnormal forebrain morphology'),
(406181, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0140065', 'abnormally necrotic ventral pallidum', 0.4027777777777778, 8.02346099791745, 1.7976851200440698, 'HP:0002060', 'Abnormal cerebral morphology'),
(406182, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0129909', 'increased size of the pallium', 0.4142857142857143, 8.02346099791745, 1.8231854734408677, 'HP:0002060', 'Abnormal cerebral morphology'),
(406183, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0140421', 'abnormally necrotic anterior entopeduncular region', 0.453125, 8.02346099791745, 1.9067330082319718, 'HP:0002060', 'Abnormal cerebral morphology'),
(406184, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0128482', 'decreased size of the ventral pallium', 0.4084507042253521, 8.02346099791745, 1.810300608993995, 'HP:0002060', 'Abnormal cerebral morphology'),
(406185, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0101496', 'abnormal subcommissural organ', 0.45, 6.667568321314008, 1.7321679319833003, 'HP:0100547', 'Abnormal forebrain morphology'),
(406186, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0103200', 'abnormal prosomere 5 morphology', 0.43283582089552236, 8.02346099791745, 1.8635560972122107, 'HP:0002060', 'Abnormal cerebral morphology'),
(406187, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0102249', 'abnormal forebrain morphology', 0.4426229508196721, 6.667568321314008, 1.7179111633526845, 'HP:0100547', 'Abnormal forebrain morphology'),
(406188, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0128739', 'decreased size of the dorsal telencephalon', 0.4142857142857143, 8.02346099791745, 1.8231854734408677, 'HP:0002060', 'Abnormal cerebral morphology'),
(406189, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0102968', 'abnormal medial ganglionic eminence morphology', 0.4461538461538462, 8.02346099791745, 1.8920089808682852, 'HP:0002060', 'Abnormal cerebral morphology'),
(406190, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0100195', 'abnormal retromammillary area', 0.45, 6.667568321314008, 1.7321679319833003, 'HP:0100547', 'Abnormal forebrain morphology'),
(406191, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0130846', 'increased size of the anterior entopeduncular region', 0.4393939393939394, 8.02346099791745, 1.8776208710622537, 'HP:0002060', 'Abnormal cerebral morphology'),
(406192, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0100473', 'abnormal ventral habenular nucleus', 0.421875, 6.667568321314008, 1.677164388351466, 'HP:0100547', 'Abnormal forebrain morphology'),
(406193, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0103040', 'abnormal nucleus of the diagonal band morphology', 0.43283582089552236, 8.02346099791745, 1.8635560972122107, 'HP:0002060', 'Abnormal cerebral morphology'),
(406194, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0140021', 'abnormally necrotic striatum', 0.4084507042253521, 8.02346099791745, 1.810300608993995, 'HP:0002060', 'Abnormal cerebral morphology'),
(406195, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0130217', 'increased size of the dorsal telencephalon', 0.4142857142857143, 8.02346099791745, 1.8231854734408677, 'HP:0002060', 'Abnormal cerebral morphology'),
(406196, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0102247', 'abnormal mitral cell layer of the olfactory bulb morphology', 0.42857142857142855, 8.651717009412357, 1.9255852924032166, 'UPHENO:0087531', 'abnormal cerebral hemisphere morphology'),
(406197, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0102490', 'abnormal presumptive midbrain-hindbrain boundary morphology', 0.4117647058823529, 5.483278994082134, 1.502604659339613, 'HP:0002011', 'Morphological central nervous system abnormality'),
(406198, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0107380', 'abnormal dorsal telencephalon morphology', 0.4603174603174603, 8.02346099791745, 1.9218062310018553, 'HP:0002060', 'Abnormal cerebral morphology'),
(406199, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0102395', 'abnormal pretectum morphology', 0.40298507462686567, 6.667568321314008, 1.639185931352649, 'HP:0100547', 'Abnormal forebrain morphology'),
(406200, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0127531', 'abnormally localised pretectum', 0.40298507462686567, 6.667568321314008, 1.639185931352649, 'HP:0100547', 'Abnormal forebrain morphology'),
(406201, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0128766', 'decreased size of the dorsal pallium', 0.4084507042253521, 8.02346099791745, 1.810300608993995, 'HP:0002060', 'Abnormal cerebral morphology'),
(406202, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0100575', 'abnormal diencephalon', 0.46551724137931033, 6.667568321314008, 1.7617797852303152, 'HP:0100547', 'Abnormal forebrain morphology'),
(406203, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0102696', 'abnormal accessory olfactory bulb morphology', 0.43478260869565216, 8.651717009412357, 1.9394886158595648, 'UPHENO:0087531', 'abnormal cerebral hemisphere morphology'),
(406204, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0100988', 'abnormal habenula', 0.4426229508196721, 6.667568321314008, 1.7179111633526845, 'HP:0100547', 'Abnormal forebrain morphology'),
(406205, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0140476', 'abnormally necrotic lateral ganglionic eminence', 0.4142857142857143, 8.02346099791745, 1.8231854734408677, 'HP:0002060', 'Abnormal cerebral morphology'),
(406206, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0129399', 'decreased size of the medial pallium', 0.4084507042253521, 8.02346099791745, 1.810300608993995, 'HP:0002060', 'Abnormal cerebral morphology'),
(406207, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0103133', 'abnormal parabrachial area morphology', 0.42, 5.483278994082134, 1.5175563177406288, 'HP:0002011', 'Morphological central nervous system abnormality'),
(406208, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0129080', 'decreased size of the medial ganglionic eminence', 0.4027777777777778, 8.02346099791745, 1.7976851200440698, 'HP:0002060', 'Abnormal cerebral morphology'),
(406209, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0100656', 'abnormal ventral hypothalamic nucleus', 0.43548387096774194, 6.667568321314008, 1.704000722566664, 'HP:0100547', 'Abnormal forebrain morphology'),
(406210, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0139993', 'abnormally necrotic pallidum', 0.4084507042253521, 8.02346099791745, 1.810300608993995, 'HP:0002060', 'Abnormal cerebral morphology'),
(406211, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0129372', 'decreased size of the anterior entopeduncular region', 0.4393939393939394, 8.02346099791745, 1.8776208710622537, 'HP:0002060', 'Abnormal cerebral morphology'),
(406212, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0102594', 'abnormal dorsal thalamus morphology', 0.40298507462686567, 6.667568321314008, 1.639185931352649, 'HP:0100547', 'Abnormal forebrain morphology'),
(406213, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0101117', 'abnormal tuberal region', 0.4426229508196721, 6.667568321314008, 1.7179111633526845, 'HP:0100547', 'Abnormal forebrain morphology'),
(406214, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0140226', 'abnormally necrotic subpallium', 0.4264705882352941, 8.02346099791745, 1.8498027277157947, 'HP:0002060', 'Abnormal cerebral morphology'),
(406215, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0130603', 'increased size of the lateral ganglionic eminence', 0.4027777777777778, 8.02346099791745, 1.7976851200440698, 'HP:0002060', 'Abnormal cerebral morphology'),
(406216, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0102191', 'abnormal telencephalon morphology', 0.46774193548387094, 8.02346099791745, 1.9372426736073256, 'HP:0002060', 'Abnormal cerebral morphology'),
(406217, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0101053', 'abnormal anterior hypothalamus', 0.45, 6.667568321314008, 1.7321679319833003, 'HP:0100547', 'Abnormal forebrain morphology'),
(406218, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0101671', 'abnormal olfactory bulb morphology', 0.42857142857142855, 8.651717009412357, 1.9255852924032166, 'UPHENO:0087531', 'abnormal cerebral hemisphere morphology'),
(406219, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0129127', 'decreased size of the lateral ganglionic eminence', 0.4027777777777778, 8.02346099791745, 1.7976851200440698, 'HP:0002060', 'Abnormal cerebral morphology'),
(406220, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0128708', 'decreased size of the basal forebrain', 0.4142857142857143, 8.02346099791745, 1.8231854734408677, 'HP:0002060', 'Abnormal cerebral morphology'),
(406221, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0100315', 'abnormal neurohypophysis', 0.43548387096774194, 6.667568321314008, 1.704000722566664, 'HP:0100547', 'Abnormal forebrain morphology'),
(406222, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0102361', 'abnormal thalamus morphology', 0.4090909090909091, 6.667568321314008, 1.6515573214369805, 'HP:0100547', 'Abnormal forebrain morphology'),
(406223, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0129756', 'increased size of the amygdala', 0.4027777777777778, 8.02346099791745, 1.7976851200440698, 'HP:0002060', 'Abnormal cerebral morphology'),
(406224, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0102951', 'abnormal lateral amygdala morphology', 0.4264705882352941, 8.02346099791745, 1.8498027277157947, 'HP:0002060', 'Abnormal cerebral morphology'),
(406225, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0101443', 'abnormal subthalamic nucleus', 0.4090909090909091, 6.667568321314008, 1.6515573214369805, 'HP:0100547', 'Abnormal forebrain morphology'),
(406226, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0100763', 'abnormal pretectum', 0.4576271186440678, 6.667568321314008, 1.7467856420423753, 'HP:0100547', 'Abnormal forebrain morphology'),
(406227, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0140571', 'abnormally necrotic medial pallium', 0.42028985507246375, 8.02346099791745, 1.8363494384224073, 'HP:0002060', 'Abnormal cerebral morphology'),
(406228, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0101351', 'abnormal dorsal habenular nucleus', 0.421875, 6.667568321314008, 1.677164388351466, 'HP:0100547', 'Abnormal forebrain morphology'),
(406229, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0100962', 'abnormal dorsal thalamus', 0.45, 6.667568321314008, 1.7321679319833003, 'HP:0100547', 'Abnormal forebrain morphology'),
(406230, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0103102', 'abnormal anterior amygdala morphology', 0.4264705882352941, 8.02346099791745, 1.8498027277157947, 'HP:0002060', 'Abnormal cerebral morphology'),
(406231, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0101825', 'abnormal granule cell layer of the olfactory bulb morphology', 0.42857142857142855, 8.651717009412357, 1.9255852924032166, 'UPHENO:0087531', 'abnormal cerebral hemisphere morphology'),
(406232, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0130903', 'increased size of the anterior commissure', 0.4084507042253521, 8.02346099791745, 1.810300608993995, 'HP:0002060', 'Abnormal cerebral morphology'),
(406233, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0101987', 'abnormal striatum morphology', 0.4393939393939394, 8.02346099791745, 1.8776208710622537, 'HP:0002060', 'Abnormal cerebral morphology'),
(406234, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0100590', 'abnormal hypothalamus', 0.4576271186440678, 6.667568321314008, 1.7467856420423753, 'HP:0100547', 'Abnormal forebrain morphology'),
(406235, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0102389', 'abnormal bed nucleus of the stria terminalis morphology', 0.43478260869565216, 8.651717009412357, 1.9394886158595648, 'UPHENO:0087531', 'abnormal cerebral hemisphere morphology'),
(406236, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0141224', 'abnormally necrotic dorsal telencephalon', 0.4264705882352941, 8.02346099791745, 1.8498027277157947, 'HP:0002060', 'Abnormal cerebral morphology'),
(406237, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0102755', 'abnormal third ventricle morphology', 0.40298507462686567, 6.667568321314008, 1.639185931352649, 'HP:0100547', 'Abnormal forebrain morphology'),
(406238, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0101068', 'abnormal pineal gland', 0.4153846153846154, 6.667568321314008, 1.6642131181731699, 'HP:0100547', 'Abnormal forebrain morphology'),
(406239, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0100783', 'abnormal supraoptoparaventricular region', 0.42857142857142855, 6.667568321314008, 1.6904228111816126, 'HP:0100547', 'Abnormal forebrain morphology'),
(406240, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0131746', 'abnormal neural tube closure', 0.42, 5.483278994082134, 1.5175563177406288, 'HP:0002011', 'Morphological central nervous system abnormality'),
(406241, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0100909', 'abnormal choroid fissure', 0.4153846153846154, 6.667568321314008, 1.6642131181731699, 'HP:0100547', 'Abnormal forebrain morphology'),
(406242, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0102207', 'abnormal diencephalon morphology', 0.4153846153846154, 6.667568321314008, 1.6642131181731699, 'HP:0100547', 'Abnormal forebrain morphology'),
(406243, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0102604', 'abnormal ventral pallidum morphology', 0.43283582089552236, 8.02346099791745, 1.8635560972122107, 'HP:0002060', 'Abnormal cerebral morphology'),
(406244, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0102584', 'abnormal dorsal septum morphology', 0.4264705882352941, 8.02346099791745, 1.8498027277157947, 'HP:0002060', 'Abnormal cerebral morphology'),
(406245, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0141149', 'abnormally necrotic dorsal pallium', 0.42028985507246375, 8.02346099791745, 1.8363494384224073, 'HP:0002060', 'Abnormal cerebral morphology'),
(406246, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0128187', 'decreased size of the basal ganglion', 0.4027777777777778, 8.02346099791745, 1.7976851200440698, 'HP:0002060', 'Abnormal cerebral morphology'),
(406247, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0130183', 'increased size of the lateral pallium', 0.4084507042253521, 8.02346099791745, 1.810300608993995, 'HP:0002060', 'Abnormal cerebral morphology'),
(406248, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0101268', 'abnormal lateral hypothalamic nucleus', 0.43548387096774194, 6.667568321314008, 1.704000722566664, 'HP:0100547', 'Abnormal forebrain morphology'),
(406249, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0140554', 'abnormally necrotic central amygdala', 0.40963855421686746, 10.854497839006713, 2.108653788918613, 'HP:0034221', 'Abnormal temporal lobe morphology'),
(406250, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0101906', 'abnormal sensory system morphology', 0.41304347826086957, 4.7814666189787065, 1.405330425021534, 'HP:0012639', 'Abnormal nervous system morphology'),
(406251, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0140838', 'abnormally necrotic anterior commissure', 0.42028985507246375, 8.02346099791745, 1.8363494384224073, 'HP:0002060', 'Abnormal cerebral morphology'),
(406252, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0129962', 'increased size of the ventral pallium', 0.4084507042253521, 8.02346099791745, 1.810300608993995, 'HP:0002060', 'Abnormal cerebral morphology'),
(406253, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0100233', 'abnormal pars nervosa', 0.42857142857142855, 6.667568321314008, 1.6904228111816126, 'HP:0100547', 'Abnormal forebrain morphology'),
(406254, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0101595', 'abnormal prosomere 4', 0.4426229508196721, 6.667568321314008, 1.7179111633526845, 'HP:0100547', 'Abnormal forebrain morphology'),
(406255, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0127764', 'abnormally localised optic chiasm', 0.40298507462686567, 6.667568321314008, 1.639185931352649, 'HP:0100547', 'Abnormal forebrain morphology'),
(406256, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0102509', 'abnormal lateral septum morphology', 0.4264705882352941, 8.02346099791745, 1.8498027277157947, 'HP:0002060', 'Abnormal cerebral morphology'),
(406257, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0101075', 'abnormal mammilary region', 0.4426229508196721, 6.667568321314008, 1.7179111633526845, 'HP:0100547', 'Abnormal forebrain morphology'),
(406258, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0101838', 'abnormal nucleus accumbens morphology', 0.42028985507246375, 8.02346099791745, 1.8363494384224073, 'HP:0002060', 'Abnormal cerebral morphology'),
(406259, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0127516', 'abnormally localised eminentia thalami', 0.40298507462686567, 6.667568321314008, 1.639185931352649, 'HP:0100547', 'Abnormal forebrain morphology'),
(406260, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0127143', 'abnormally localised thalamus', 0.40298507462686567, 6.667568321314008, 1.639185931352649, 'HP:0100547', 'Abnormal forebrain morphology'),
(406261, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0142058', 'abnormal cerebrospinal fluid morphology', 0.45652173913043476, 5.483278994082134, 1.5821618319614958, 'HP:0002011', 'Morphological central nervous system abnormality'),
(406262, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0128276', 'decreased size of the amygdala', 0.4027777777777778, 8.02346099791745, 1.7976851200440698, 'HP:0002060', 'Abnormal cerebral morphology'),
(406263, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0142037', 'decreased size of the cerebrospinal fluid', 0.4117647058823529, 5.483278994082134, 1.502604659339613, 'HP:0002011', 'Morphological central nervous system abnormality'),
(406264, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0101797', 'abnormal lateral pallium morphology', 0.453125, 8.02346099791745, 1.9067330082319718, 'HP:0002060', 'Abnormal cerebral morphology'),
(406265, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0101564', 'abnormal anterior thalamic nucleus', 0.43548387096774194, 6.667568321314008, 1.704000722566664, 'HP:0100547', 'Abnormal forebrain morphology'),
(406266, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0102442', 'abnormal medial pallium morphology', 0.453125, 8.02346099791745, 1.9067330082319718, 'HP:0002060', 'Abnormal cerebral morphology'),
(406267, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0101851', 'abnormal basal ganglion morphology', 0.4461538461538462, 8.02346099791745, 1.8920089808682852, 'HP:0002060', 'Abnormal cerebral morphology'),
(406268, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0140020', 'abnormally necrotic amygdala', 0.4142857142857143, 8.02346099791745, 1.8231854734408677, 'HP:0002060', 'Abnormal cerebral morphology'),
(406269, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0102760', 'abnormal dorsal pallidum morphology', 0.43283582089552236, 8.02346099791745, 1.8635560972122107, 'HP:0002060', 'Abnormal cerebral morphology'),
(406270, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0101790', 'abnormal neuromere morphology', 0.42857142857142855, 5.483278994082134, 1.5329633758669794, 'HP:0002011', 'Morphological central nervous system abnormality'),
(406271, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0130187', 'increased size of the basal forebrain', 0.4142857142857143, 8.02346099791745, 1.8231854734408677, 'HP:0002060', 'Abnormal cerebral morphology'),
(406272, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0100194', 'abnormal preoptic area', 0.4426229508196721, 6.667568321314008, 1.7179111633526845, 'HP:0100547', 'Abnormal forebrain morphology'),
(406273, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0100698', 'abnormal optic stalk', 0.4426229508196721, 6.667568321314008, 1.7179111633526845, 'HP:0100547', 'Abnormal forebrain morphology'),
(406274, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0100491', 'abnormal pars distalis', 0.42857142857142855, 6.667568321314008, 1.6904228111816126, 'HP:0100547', 'Abnormal forebrain morphology'),
(406275, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0141259', 'abnormally necrotic accessory olfactory bulb', 0.40540540540540543, 8.651717009412357, 1.872819489874467, 'UPHENO:0087531', 'abnormal cerebral hemisphere morphology'),
(406276, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0130873', 'increased size of the medial pallium', 0.4084507042253521, 8.02346099791745, 1.810300608993995, 'HP:0002060', 'Abnormal cerebral morphology'),
(406277, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0101866', 'abnormal anterior entopeduncular nucleus morphology', 0.42028985507246375, 8.02346099791745, 1.8363494384224073, 'HP:0002060', 'Abnormal cerebral morphology'),
(406278, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0102826', 'abnormal anterior commissure morphology', 0.453125, 8.02346099791745, 1.9067330082319718, 'HP:0002060', 'Abnormal cerebral morphology'),
(406279, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0128429', 'decreased size of the pallium', 0.4142857142857143, 8.02346099791745, 1.8231854734408677, 'HP:0002060', 'Abnormal cerebral morphology'),
(406280, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0142044', 'increased size of the cerebrospinal fluid', 0.4117647058823529, 5.483278994082134, 1.502604659339613, 'HP:0002011', 'Morphological central nervous system abnormality'),
(406281, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0101663', 'abnormal central nervous system morphology', 0.44680851063829785, 5.483278994082134, 1.5652398285119449, 'HP:0002011', 'Morphological central nervous system abnormality'),
(406282, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0100263', 'abnormal prethalamus', 0.45, 6.667568321314008, 1.7321679319833003, 'HP:0100547', 'Abnormal forebrain morphology'),
(406283, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0101186', 'abnormal optic chiasm', 0.4576271186440678, 6.667568321314008, 1.7467856420423753, 'HP:0100547', 'Abnormal forebrain morphology'),
(406284, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0129429', 'decreased size of the anterior commissure', 0.4084507042253521, 8.02346099791745, 1.810300608993995, 'HP:0002060', 'Abnormal cerebral morphology'),
(406285, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0128704', 'decreased size of the lateral pallium', 0.4084507042253521, 8.02346099791745, 1.810300608993995, 'HP:0002060', 'Abnormal cerebral morphology'),
(406286, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0103178', 'abnormal dorsal pallium morphology', 0.453125, 8.02346099791745, 1.9067330082319718, 'HP:0002060', 'Abnormal cerebral morphology'),
(406287, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0102007', 'abnormal anterior entopeduncular region morphology', 0.47540983606557374, 8.02346099791745, 1.9530571619126922, 'HP:0002060', 'Abnormal cerebral morphology'),
(406288, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0142031', 'abnormally necrotic cerebrospinal fluid', 0.42857142857142855, 5.483278994082134, 1.5329633758669794, 'HP:0002011', 'Morphological central nervous system abnormality'),
(406289, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0140045', 'abnormally necrotic lateral pallium', 0.42028985507246375, 8.02346099791745, 1.8363494384224073, 'HP:0002060', 'Abnormal cerebral morphology'),
(406290, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0102986', 'abnormal eminentia thalami morphology', 0.4090909090909091, 6.667568321314008, 1.6515573214369805, 'HP:0100547', 'Abnormal forebrain morphology'),
(406291, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0103107', 'abnormal ventral septum morphology', 0.4264705882352941, 8.02346099791745, 1.8498027277157947, 'HP:0002060', 'Abnormal cerebral morphology'),
(406292, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0128602', 'decreased size of the subpallium', 0.4142857142857143, 8.02346099791745, 1.8231854734408677, 'HP:0002060', 'Abnormal cerebral morphology'),
(406293, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0127949', 'abnormally localised optic tract', 0.40298507462686567, 6.667568321314008, 1.639185931352649, 'HP:0100547', 'Abnormal forebrain morphology'),
(406294, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0100946', 'abnormal melanotrope', 0.4153846153846154, 6.667568321314008, 1.6642131181731699, 'HP:0100547', 'Abnormal forebrain morphology'),
(406295, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0101526', 'abnormal infundibulum', 0.4426229508196721, 6.667568321314008, 1.7179111633526845, 'HP:0100547', 'Abnormal forebrain morphology'),
(406296, 'HP:0034222', 'Temporal lobe dysplasia', 'XPO:0102978', 'abnormal prosomere 6 morphology', 0.43283582089552236, 8.02346099791745, 1.8635560972122107, 'HP:0002060', 'Abnormal cerebral morphology'),
(406297, 'HP:0025497', 'Coronary artery spasm', 'XPO:0101583', 'abnormal truncus arteriosus', 0.41025641025641024, 5.809304221129108, 1.5437954190396599, 'UPHENO:0002678', 'abnormal vasculature'),
(406298, 'HP:0025497', 'Coronary artery spasm', 'XPO:0100043', 'abnormal vein', 0.41025641025641024, 5.809304221129108, 1.5437954190396599, 'UPHENO:0002678', 'abnormal vasculature'),
(406299, 'HP:0025497', 'Coronary artery spasm', 'XPO:0100981', 'abnormal dorsal longitudinal anastomosing vessel', 0.41025641025641024, 5.809304221129108, 1.5437954190396599, 'UPHENO:0002678', 'abnormal vasculature'),
(406300, 'HP:0025497', 'Coronary artery spasm', 'XPO:0100076', 'abnormal artery', 0.41025641025641024, 5.809304221129108, 1.5437954190396599, 'UPHENO:0002678', 'abnormal vasculature'),
(406301, 'HP:0025497', 'Coronary artery spasm', 'XPO:0100780', 'abnormal vascular plexus', 0.41025641025641024, 5.809304221129108, 1.5437954190396599, 'UPHENO:0002678', 'abnormal vasculature'),
(406302, 'HP:0025497', 'Coronary artery spasm', 'XPO:0100792', 'abnormal capillary', 0.41025641025641024, 5.809304221129108, 1.5437954190396599, 'UPHENO:0002678', 'abnormal vasculature'),
(406303, 'HP:0025497', 'Coronary artery spasm', 'XPO:0100054', 'abnormal blood vessel', 0.42105263157894735, 5.809304221129108, 1.5639766078650594, 'UPHENO:0002678', 'abnormal vasculature'),
(406304, 'HP:0012034', 'Liposarcoma', 'XPO:0100910', 'abnormal vacuolated notochordal tissue', 0.42424242424242425, 6.985637650836012, 1.721512082986879, 'UPHENO:0002712', 'abnormal connective tissue'),
(406305, 'HP:0012034', 'Liposarcoma', 'XPO:0107288', 'abnormal larval alimentary system', 0.41935483870967744, 4.970960464763942, 1.4438131194629262, 'HP:0011793', 'Neoplasm by anatomical site'),
(406306, 'HP:0012034', 'Liposarcoma', 'XPO:0102009', 'abnormal connective tissue morphology', 0.42857142857142855, 6.985637650836012, 1.7302730153074537, 'UPHENO:0002712', 'abnormal connective tissue'),
(406307, 'HP:0012034', 'Liposarcoma', 'XPO:0100378', 'abnormal perichondrium', 0.45161290322580644, 6.985637650836012, 1.7761768212589517, 'UPHENO:0002712', 'abnormal connective tissue'),
(406308, 'HP:0012034', 'Liposarcoma', 'XPO:0101096', 'abnormal tendon', 0.4666666666666667, 6.985637650836012, 1.805537104868467, 'UPHENO:0002712', 'abnormal connective tissue'),
(406309, 'HP:0012034', 'Liposarcoma', 'XPO:0100493', 'abnormal liver and biliary system', 0.41935483870967744, 4.970960464763942, 1.4438131194629262, 'HP:0011793', 'Neoplasm by anatomical site'),
(406310, 'HP:0012034', 'Liposarcoma', 'XPO:0102049', 'abnormal dense regular connective tissue morphology', 0.40540540540540543, 6.985637650836012, 1.6828592525379054, 'UPHENO:0002712', 'abnormal connective tissue'),
(406311, 'HP:0012034', 'Liposarcoma', 'XPO:0100377', 'abnormal connective tissue', 0.5, 6.985637650836012, 1.8689084582766504, 'UPHENO:0002712', 'abnormal connective tissue'),
(406312, 'HP:0012034', 'Liposarcoma', 'XPO:0115491', 'abnormally increased distribution of connective tissue', 0.4166666666666667, 6.985637650836012, 1.70607220085054, 'UPHENO:0002712', 'abnormal connective tissue'),
(406313, 'HP:0012034', 'Liposarcoma', 'XPO:0142054', 'abnormal digestive tract', 0.40625, 4.970960464763942, 1.4210744839065794, 'HP:0011793', 'Neoplasm by anatomical site'),
(406314, 'HP:0012034', 'Liposarcoma', 'XPO:0100416', 'abnormal ligament', 0.4666666666666667, 6.985637650836012, 1.805537104868467, 'UPHENO:0002712', 'abnormal connective tissue'),
(406315, 'HP:0012034', 'Liposarcoma', 'XPO:0101602', 'abnormal intersomitic tendon', 0.42424242424242425, 6.985637650836012, 1.721512082986879, 'UPHENO:0002712', 'abnormal connective tissue'),
(406316, 'HP:0012034', 'Liposarcoma', 'XPO:0100152', 'abnormal alimentary system', 0.43333333333333335, 4.970960464763942, 1.4676794159707953, 'HP:0011793', 'Neoplasm by anatomical site'),
(406317, 'HP:0012034', 'Liposarcoma', 'XPO:0100417', 'abnormal dense regular connective tissue', 0.4827586206896552, 6.985637650836012, 1.836403222866731, 'UPHENO:0002712', 'abnormal connective tissue'),
(406318, 'HP:0012034', 'Liposarcoma', 'XPO:0100688', 'abnormal adipose tissue', 0.4827586206896552, 6.985637650836012, 1.836403222866731, 'UPHENO:0002712', 'abnormal connective tissue'),
(406319, 'HP:0012034', 'Liposarcoma', 'XPO:0100993', 'abnormal ligament cell', 0.4117647058823529, 6.985637650836012, 1.6960067902862834, 'UPHENO:0002712', 'abnormal connective tissue'),
(406320, 'HP:0012034', 'Liposarcoma', 'XPO:0101162', 'abnormal stromal cell', 0.4375, 6.985637650836012, 1.748203784528782, 'UPHENO:0002712', 'abnormal connective tissue'),
(406321, 'HP:0012034', 'Liposarcoma', 'XPO:0101493', 'abnormal fat body', 0.4117647058823529, 6.985637650836012, 1.6960067902862834, 'UPHENO:0002712', 'abnormal connective tissue'),
(406322, 'HP:0012034', 'Liposarcoma', 'XPO:0115391', 'abnormally undifferentiated alimentary system', 0.41935483870967744, 4.970960464763942, 1.4438131194629262, 'HP:0011793', 'Neoplasm by anatomical site'),
(406323, 'HP:0012034', 'Liposarcoma', 'XPO:0102320', 'abnormal adipose tissue morphology', 0.4594594594594595, 10.114017760664272, 2.1556857686773783, 'UPHENO:0076797', 'abnormal adipose tissue morphology'),
(406324, 'HP:0012034', 'Liposarcoma', 'XPO:0100890', 'abnormal pharyngeal cavity', 0.40625, 4.970960464763942, 1.4210744839065794, 'HP:0011793', 'Neoplasm by anatomical site'),
(406325, 'HP:0012034', 'Liposarcoma', 'XPO:0101348', 'abnormal perichordal tissue', 0.42424242424242425, 6.985637650836012, 1.721512082986879, 'UPHENO:0002712', 'abnormal connective tissue'),
(406326, 'HP:0003498', 'Disproportionate short stature', 'XPO:0103371', 'decreased size of the whole organism', 0.45, 11.964122330181212, 2.3203135668658117, 'UPHENO:0069254', 'decreased size of the multicellular organism'),
(406327, 'HP:0003498', 'Disproportionate short stature', 'XPO:0141485', 'decreased size of the tadpole', 0.4186046511627907, 11.964122330181212, 2.2379091256113286, 'UPHENO:0069254', 'decreased size of the multicellular organism'),
(406328, 'HP:0003498', 'Disproportionate short stature', 'XPO:0103579', 'decreased length of trunk', 0.5076923076923077, 13.568193653850074, 2.6245890244644525, 'HP:0003498', 'Disproportionate short stature'),
(406329, 'HP:0003498', 'Disproportionate short stature', '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'),
(406330, 'HP:0003498', 'Disproportionate short stature', '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'),
(406331, 'HP:0003498', 'Disproportionate short stature', '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'),
(406332, 'HP:0003498', 'Disproportionate short stature', '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'),
(406333, 'HP:0003498', 'Disproportionate short stature', 'XPO:0103567', 'decreased length of forelimb', 0.4852941176470588, 13.568193653850074, 2.5660406402295335, 'HP:0003498', 'Disproportionate short stature'),
(406334, 'HP:0003498', 'Disproportionate short stature', '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'),
(406335, 'HP:0003498', 'Disproportionate short stature', 'XPO:0128400', 'decreased size of the male organism', 0.4186046511627907, 11.964122330181212, 2.2379091256113286, 'UPHENO:0069254', 'decreased size of the multicellular organism'),
(406336, 'HP:0003498', 'Disproportionate short stature', 'XPO:0129133', 'decreased size of the female organism', 0.4186046511627907, 11.964122330181212, 2.2379091256113286, 'UPHENO:0069254', 'decreased size of the multicellular organism'),
(406337, 'HP:0003498', 'Disproportionate short stature', 'XPO:0103570', 'decreased length of hindlimb', 0.4925373134328358, 13.568193653850074, 2.585119271988, 'HP:0003498', 'Disproportionate short stature'),
(406338, 'HP:0003498', 'Disproportionate short stature', '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'),
(406339, 'HP:0020135', 'Myofibromatosis', 'XPO:0100791', 'abnormal multiciliated cell precursor', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(406340, 'HP:0020135', 'Myofibromatosis', 'XPO:0100026', 'abnormal germ cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(406341, 'HP:0020135', 'Myofibromatosis', 'XPO:0100621', 'abnormal peritoneum', 0.41379310344827586, 4.970960464763942, 1.43420680441607, 'HP:0011793', 'Neoplasm by anatomical site'),
(406342, 'HP:0020135', 'Myofibromatosis', 'XPO:0141276', 'decreased surface breathing', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406343, 'HP:0020135', 'Myofibromatosis', 'XPO:0100437', 'abnormal proepicardium', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(406344, 'HP:0020135', 'Myofibromatosis', 'XPO:0100917', 'abnormal stage III oocyte', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(406345, 'HP:0020135', 'Myofibromatosis', 'XPO:0107304', 'abnormal hindgut endoderm', 0.41379310344827586, 4.970960464763942, 1.43420680441607, 'HP:0011793', 'Neoplasm by anatomical site'),
(406346, 'HP:0020135', 'Myofibromatosis', 'XPO:0100492', 'abnormal gall bladder primordium', 0.41379310344827586, 4.970960464763942, 1.43420680441607, 'HP:0011793', 'Neoplasm by anatomical site'),
(406347, 'HP:0020135', 'Myofibromatosis', 'XPO:0100084', 'abnormal anatomical group', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406348, 'HP:0020135', 'Myofibromatosis', 'XPO:0100239', 'abnormal acellular anatomical structure', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406349, 'HP:0020135', 'Myofibromatosis', 'XPO:0101221', 'abnormal larval immune system', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(406350, 'HP:0020135', 'Myofibromatosis', 'XPO:0101601', 'abnormal proctodeum', 0.42857142857142855, 4.970960464763942, 1.4595929664656426, 'HP:0011793', 'Neoplasm by anatomical site'),
(406351, 'HP:0020135', 'Myofibromatosis', 'XPO:0141271', 'increased surface breathing', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406352, 'HP:0020135', 'Myofibromatosis', 'XPO:0101569', 'abnormal activin-induced ectoderm', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406353, 'HP:0020135', 'Myofibromatosis', 'XPO:0141791', 'abnormal primary metabolic process', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(406354, 'HP:0020135', 'Myofibromatosis', 'XPO:0107312', 'abnormal filopodium', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(406355, 'HP:0020135', 'Myofibromatosis', 'XPO:0131675', 'abnormal spindle microtubule', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(406356, 'HP:0020135', 'Myofibromatosis', 'XPO:0100477', 'abnormal pericyte', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(406357, 'HP:0020135', 'Myofibromatosis', 'XPO:0141600', 'absent metamorphosis', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406358, 'HP:0020135', 'Myofibromatosis', 'XPO:0131729', 'abnormal regulation of growth rate', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406359, 'HP:0020135', 'Myofibromatosis', 'XPO:0133388', 'absent insulin receptor signaling pathway', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406360, 'HP:0020135', 'Myofibromatosis', 'XPO:0101435', 'abnormal paracrine cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(406361, 'HP:0020135', 'Myofibromatosis', 'XPO:0100031', 'abnormal central nervous system', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(406362, 'HP:0020135', 'Myofibromatosis', 'XPO:0107261', 'abnormal dorsal-ventral axis', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406363, 'HP:0020135', 'Myofibromatosis', 'XPO:0131723', 'abnormal pathway-restricted SMAD protein phosphorylation', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406364, 'HP:0020135', 'Myofibromatosis', 'XPO:0100546', 'abnormal whole organism', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406365, 'HP:0020135', 'Myofibromatosis', 'XPO:0131685', 'abnormal cortical actin cytoskeleton', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(406366, 'HP:0020135', 'Myofibromatosis', 'XPO:0100894', 'abnormal nucleus', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(406367, 'HP:0020135', 'Myofibromatosis', 'XPO:0101021', 'abnormal dorsal foregut', 0.4444444444444444, 4.970960464763942, 1.4863767228119886, 'HP:0011793', 'Neoplasm by anatomical site'),
(406368, 'HP:0020135', 'Myofibromatosis', 'XPO:0141790', 'abnormal cellular metabolic process', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(406369, 'HP:0020135', 'Myofibromatosis', 'XPO:0107262', 'abnormal left-right axis', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406370, 'HP:0020135', 'Myofibromatosis', 'XPO:0100802', 'abnormal exocrine cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(406371, 'HP:0020135', 'Myofibromatosis', 'XPO:0107288', 'abnormal larval alimentary system', 0.5, 4.970960464763942, 1.5765405901472918, 'HP:0011793', 'Neoplasm by anatomical site'),
(406372, 'HP:0020135', 'Myofibromatosis', 'XPO:0141796', 'abnormal demethylation', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(406373, 'HP:0020135', 'Myofibromatosis', 'XPO:0141781', 'abnormal secondary metabolic process', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(406374, 'HP:0020135', 'Myofibromatosis', 'XPO:0101326', 'abnormal cementoblast', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(406375, 'HP:0020135', 'Myofibromatosis', 'XPO:0100986', 'abnormal gut epithelium', 0.4444444444444444, 4.970960464763942, 1.4863767228119886, 'HP:0011793', 'Neoplasm by anatomical site'),
(406376, 'HP:0020135', 'Myofibromatosis', 'XPO:0100032', 'abnormal nervous system', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(406377, 'HP:0020135', 'Myofibromatosis', 'XPO:0101228', 'abnormal mesenchymal stem cell', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(406378, 'HP:0020135', 'Myofibromatosis', 'XPO:00000000', 'Xenopus phenotype', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406379, 'HP:0020135', 'Myofibromatosis', 'XPO:0100573', 'abnormal extraembryonic structure', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406380, 'HP:0020135', 'Myofibromatosis', 'XPO:0101498', 'abnormal stage II oocyte', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(406381, 'HP:0020135', 'Myofibromatosis', 'XPO:0100653', 'abnormal myoblast', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(406382, 'HP:0020135', 'Myofibromatosis', 'XPO:0101109', 'abnormal egg cell-free extract', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406383, 'HP:0020135', 'Myofibromatosis', 'XPO:0101169', 'abnormal hepato-pancreatic duct', 0.42857142857142855, 4.970960464763942, 1.4595929664656426, 'HP:0011793', 'Neoplasm by anatomical site'),
(406384, 'HP:0020135', 'Myofibromatosis', 'XPO:0141907', 'abnormal putrescine metabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(406385, 'HP:0020135', 'Myofibromatosis', 'XPO:0100486', 'abnormal oral evagination', 0.46153846153846156, 4.970960464763942, 1.5146912045944103, 'HP:0011793', 'Neoplasm by anatomical site'),
(406386, 'HP:0020135', 'Myofibromatosis', 'XPO:0141792', 'abnormal small molecule metabolic process', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(406387, 'HP:0020135', 'Myofibromatosis', 'XPO:0100721', 'abnormal centromere', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(406388, 'HP:0020135', 'Myofibromatosis', 'XPO:0100852', 'abnormal interdigital region', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(406389, 'HP:0020135', 'Myofibromatosis', 'XPO:0100969', 'abnormal disaggregated/reaggregated ectoderm treated with activin', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406390, 'HP:0020135', 'Myofibromatosis', 'XPO:0100890', 'abnormal pharyngeal cavity', 0.48, 4.970960464763942, 1.5446880018588518, 'HP:0011793', 'Neoplasm by anatomical site'),
(406391, 'HP:0020135', 'Myofibromatosis', 'XPO:0115509', 'abnormally semi-viable whole organism', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406392, 'HP:0020135', 'Myofibromatosis', 'XPO:0100081', 'abnormal anatomical entity in vitro', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406393, 'HP:0020135', 'Myofibromatosis', 'XPO:0141745', 'abnormal creatinine homeostasis', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406394, 'HP:0020135', 'Myofibromatosis', 'XPO:0141772', 'abnormal water homeostasis', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406395, 'HP:0020135', 'Myofibromatosis', 'XPO:0141778', 'abnormal biosynthetic process', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(406396, 'HP:0020135', 'Myofibromatosis', 'XPO:0101468', 'abnormal stage I oocyte', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(406397, 'HP:0020135', 'Myofibromatosis', 'XPO:0100172', 'abnormal stem cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(406398, 'HP:0020135', 'Myofibromatosis', 'XPO:0131469', 'abnormal heart process', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406399, 'HP:0020135', 'Myofibromatosis', 'XPO:0101448', 'abnormal myelin accumulating cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(406400, 'HP:0020135', 'Myofibromatosis', 'XPO:0101297', 'abnormal barrier cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(406401, 'HP:0020135', 'Myofibromatosis', 'XPO:0141795', 'abnormal glycosylation', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(406402, 'HP:0020135', 'Myofibromatosis', 'XPO:0100691', 'abnormal keratin accumulating cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(406403, 'HP:0020135', 'Myofibromatosis', 'XPO:0107259', 'abnormal animal-vegetal axis', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406404, 'HP:0020135', 'Myofibromatosis', 'XPO:0141315', 'abnormal anatomical region', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406405, 'HP:0020135', 'Myofibromatosis', 'XPO:0141266', 'abnormal surface breathing', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406406, 'HP:0020135', 'Myofibromatosis', 'XPO:0100754', 'abnormal electrically active cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(406407, 'HP:0020135', 'Myofibromatosis', 'XPO:0100258', 'abnormal organ part', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406408, 'HP:0020135', 'Myofibromatosis', 'XPO:0100202', 'abnormal embryo', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406409, 'HP:0020135', 'Myofibromatosis', 'XPO:0100392', 'abnormal cilium', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(406410, 'HP:0020135', 'Myofibromatosis', 'XPO:0141784', 'abnormal cellular hormone metabolic process', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406411, 'HP:0020135', 'Myofibromatosis', 'XPO:0131691', 'abnormal molecular function', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406412, 'HP:0020135', 'Myofibromatosis', 'XPO:0100735', 'abnormal hindgut', 0.46153846153846156, 4.970960464763942, 1.5146912045944103, 'HP:0011793', 'Neoplasm by anatomical site'),
(406413, 'HP:0020135', 'Myofibromatosis', 'XPO:0100377', 'abnormal connective tissue', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(406414, 'HP:0020135', 'Myofibromatosis', 'XPO:0100581', 'abnormal immune system', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(406415, 'HP:0020135', 'Myofibromatosis', 'XPO:0100907', 'abnormal cytoplasm', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(406416, 'HP:0020135', 'Myofibromatosis', 'XPO:0101237', 'abnormal mucus secreting cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(406417, 'HP:0020135', 'Myofibromatosis', 'XPO:0141787', 'abnormal hormone metabolic process', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(406418, 'HP:0020135', 'Myofibromatosis', 'XPO:0100062', 'abnormal anatomical space', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406419, 'HP:0020135', 'Myofibromatosis', 'XPO:0141794', 'abnormal prosthetic group metabolic process', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(406420, 'HP:0020135', 'Myofibromatosis', 'XPO:0141777', 'abnormal catabolic process', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(406421, 'HP:0020135', 'Myofibromatosis', 'XPO:0115508', 'abnormally peramorphic growth of whole organism', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406422, 'HP:0020135', 'Myofibromatosis', 'XPO:0141265', 'abnormal escape behavior', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406423, 'HP:0020135', 'Myofibromatosis', 'XPO:0101513', 'abnormal basal body', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(406424, 'HP:0020135', 'Myofibromatosis', 'XPO:0100599', 'abnormal adult immune system', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(406425, 'HP:0020135', 'Myofibromatosis', 'XPO:0101071', 'abnormal endoplasmic reticulum', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(406426, 'HP:0020135', 'Myofibromatosis', 'XPO:0100285', 'abnormal progenitor cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(406427, 'HP:0020135', 'Myofibromatosis', 'XPO:0100724', 'abnormal kinetochore', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(406428, 'HP:0020135', 'Myofibromatosis', 'XPO:0101333', 'abnormal barrier epithelial cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(406429, 'HP:0020135', 'Myofibromatosis', 'XPO:0100423', 'abnormal process', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406430, 'HP:0020135', 'Myofibromatosis', 'XPO:0101472', 'abnormal zygote cortex', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(406431, 'HP:0020135', 'Myofibromatosis', 'XPO:0107270', 'abnormal proximal-distal axis', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406432, 'HP:0020135', 'Myofibromatosis', 'XPO:0101157', 'abnormal female organism', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406433, 'HP:0020135', 'Myofibromatosis', 'XPO:0100462', 'abnormal anterior foregut', 0.4444444444444444, 4.970960464763942, 1.4863767228119886, 'HP:0011793', 'Neoplasm by anatomical site'),
(406434, 'HP:0020135', 'Myofibromatosis', 'XPO:0141786', 'abnormal pigment metabolic process', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(406435, 'HP:0020135', 'Myofibromatosis', 'XPO:0133403', 'abnormal developmental process', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406436, 'HP:0020135', 'Myofibromatosis', 'XPO:0100152', 'abnormal alimentary system', 0.5217391304347826, 4.970960464763942, 1.6104485680429605, 'HP:0011793', 'Neoplasm by anatomical site'),
(406437, 'HP:0020135', 'Myofibromatosis', 'XPO:0100225', 'abnormal endocrine system', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(406438, 'HP:0020135', 'Myofibromatosis', 'XPO:0100289', 'abnormal chondroblast', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(406439, 'HP:0020135', 'Myofibromatosis', 'XPO:0101366', 'abnormal morula cell', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(406440, 'HP:0020135', 'Myofibromatosis', 'XPO:0100545', 'abnormal male organism', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406441, 'HP:0020135', 'Myofibromatosis', 'XPO:0100274', 'abnormal sensory system', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(406442, 'HP:0020135', 'Myofibromatosis', 'XPO:0100317', 'abnormal respiratory system', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(406443, 'HP:0020135', 'Myofibromatosis', 'XPO:0141809', 'abnormal catalytic activity', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406444, 'HP:0020135', 'Myofibromatosis', 'XPO:0100674', 'abnormal secondary oogonium', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(406445, 'HP:0020135', 'Myofibromatosis', 'XPO:0141860', 'abnormal malate-aspartate shuttle', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(406446, 'HP:0020135', 'Myofibromatosis', 'XPO:0100549', 'abnormal mitotic cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(406447, 'HP:0020135', 'Myofibromatosis', 'XPO:0107260', 'abnormal anterior-posterior axis', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406448, 'HP:0020135', 'Myofibromatosis', 'XPO:0131677', 'abnormal actin filament', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(406449, 'HP:0020135', 'Myofibromatosis', 'XPO:0100533', 'abnormal melanoblast', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(406450, 'HP:0020135', 'Myofibromatosis', 'XPO:0101409', 'abnormal perivitelline space', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(406451, 'HP:0020135', 'Myofibromatosis', 'XPO:0100025', 'abnormal oocyte', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(406452, 'HP:0020135', 'Myofibromatosis', 'XPO:0141797', 'abnormal hydrogen metabolic process', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(406453, 'HP:0020135', 'Myofibromatosis', 'XPO:0101467', 'abnormal alkali secreting cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(406454, 'HP:0020135', 'Myofibromatosis', 'XPO:0100902', 'abnormal spermatocyte', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(406455, 'HP:0020135', 'Myofibromatosis', 'XPO:0131666', 'abnormal adherens junction', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(406456, 'HP:0020135', 'Myofibromatosis', 'XPO:0100215', 'abnormal first pancreatic bud', 0.41379310344827586, 4.970960464763942, 1.43420680441607, 'HP:0011793', 'Neoplasm by anatomical site'),
(406457, 'HP:0020135', 'Myofibromatosis', 'XPO:0101461', 'abnormal sperm entry point', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(406458, 'HP:0020135', 'Myofibromatosis', 'XPO:0131667', 'abnormal actin cytoskeleton', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(406459, 'HP:0020135', 'Myofibromatosis', 'XPO:0115391', 'abnormally undifferentiated alimentary system', 0.5, 4.970960464763942, 1.5765405901472918, 'HP:0011793', 'Neoplasm by anatomical site'),
(406460, 'HP:0020135', 'Myofibromatosis', 'XPO:0141499', 'abnormal tadpole', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406461, 'HP:0020135', 'Myofibromatosis', 'XPO:0131725', 'abnormal phosphorylation of RNA polymerase II C-terminal domain', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406462, 'HP:0020135', 'Myofibromatosis', 'XPO:0141770', 'abnormal urate homeostasis', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406463, 'HP:0020135', 'Myofibromatosis', 'XPO:0142054', 'abnormal digestive tract', 0.48, 4.970960464763942, 1.5446880018588518, 'HP:0011793', 'Neoplasm by anatomical site'),
(406464, 'HP:0020135', 'Myofibromatosis', 'XPO:0100899', 'abnormal secondary spermatogonium', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(406465, 'HP:0020135', 'Myofibromatosis', 'XPO:0141798', 'abnormal lipid metabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(406466, 'HP:0020135', 'Myofibromatosis', 'XPO:0100429', 'abnormal spermatid', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(406467, 'HP:0020135', 'Myofibromatosis', 'XPO:0100386', 'abnormal limb', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(406468, 'HP:0020135', 'Myofibromatosis', 'XPO:0115505', 'dead whole organism', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406469, 'HP:0020135', 'Myofibromatosis', 'XPO:0107284', 'abnormal migrating myoblast', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(406470, 'HP:0020135', 'Myofibromatosis', 'XPO:0100515', 'abnormal somatic stem cell', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(406471, 'HP:0020135', 'Myofibromatosis', 'XPO:0100718', 'abnormal ventral pancreatic bud', 0.42857142857142855, 4.970960464763942, 1.4595929664656426, 'HP:0011793', 'Neoplasm by anatomical site'),
(406472, 'HP:0020135', 'Myofibromatosis', 'XPO:0115512', 'abnormally semi-erect whole organism', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406473, 'HP:0020135', 'Myofibromatosis', 'XPO:0100888', 'abnormal microtubule', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(406474, 'HP:0020135', 'Myofibromatosis', 'XPO:0141743', 'abnormal chemical homeostasis within a tissue', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406475, 'HP:0020135', 'Myofibromatosis', 'XPO:0141738', 'abnormal carbon dioxide homeostasis', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406476, 'HP:0020135', 'Myofibromatosis', 'XPO:0101373', 'abnormal oxygen accumulating cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(406477, 'HP:0020135', 'Myofibromatosis', 'XPO:0116434', 'abnormal biological process', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406478, 'HP:0020135', 'Myofibromatosis', 'XPO:0141263', 'abnormal visually guided collision avoidance behavior', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406479, 'HP:0020135', 'Myofibromatosis', 'XPO:0100715', 'abnormal ciliated cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(406480, 'HP:0020135', 'Myofibromatosis', 'XPO:0101004', 'abnormal acid secreting cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(406481, 'HP:0020135', 'Myofibromatosis', 'XPO:0107253', 'abnormal enteric nervous system', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(406482, 'HP:0020135', 'Myofibromatosis', 'XPO:0101132', 'abnormal apoptotic cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(406483, 'HP:0020135', 'Myofibromatosis', 'XPO:0100523', 'abnormal midgut', 0.46153846153846156, 4.970960464763942, 1.5146912045944103, 'HP:0011793', 'Neoplasm by anatomical site'),
(406484, 'HP:0020135', 'Myofibromatosis', 'XPO:0100574', 'abnormal gastrula cell', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(406485, 'HP:0020135', 'Myofibromatosis', 'XPO:0100010', 'abnormal multicellular anatomical structure', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406486, 'HP:0020135', 'Myofibromatosis', 'XPO:0101061', 'abnormal plasma membrane', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(406487, 'HP:0020135', 'Myofibromatosis', 'XPO:0101198', 'abnormal digestive enzyme secreting cell', 0.41379310344827586, 4.970960464763942, 1.43420680441607, 'HP:0011793', 'Neoplasm by anatomical site'),
(406488, 'HP:0020135', 'Myofibromatosis', 'XPO:0100156', 'abnormal foregut', 0.46153846153846156, 4.970960464763942, 1.5146912045944103, 'HP:0011793', 'Neoplasm by anatomical site'),
(406489, 'HP:0020135', 'Myofibromatosis', 'XPO:0101101', 'abnormal posterior foregut', 0.4444444444444444, 4.970960464763942, 1.4863767228119886, 'HP:0011793', 'Neoplasm by anatomical site'),
(406490, 'HP:0020135', 'Myofibromatosis', 'XPO:0100638', 'abnormal polar body', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(406491, 'HP:0020135', 'Myofibromatosis', 'XPO:0100493', 'abnormal liver and biliary system', 0.5, 4.970960464763942, 1.5765405901472918, 'HP:0011793', 'Neoplasm by anatomical site'),
(406492, 'HP:0020135', 'Myofibromatosis', 'XPO:0107258', 'abnormal anatomical axis', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406493, 'HP:0020135', 'Myofibromatosis', 'XPO:0116494', 'absent biological process', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406494, 'HP:0020135', 'Myofibromatosis', 'XPO:0101220', 'abnormal centriole', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(406495, 'HP:0020135', 'Myofibromatosis', 'XPO:0100956', 'abnormal centrosome', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(406496, 'HP:0020135', 'Myofibromatosis', 'XPO:0141771', 'abnormal urea homeostasis', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406497, 'HP:0020135', 'Myofibromatosis', 'XPO:0101241', 'abnormal nucleate erythrocyte', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(406498, 'HP:0020135', 'Myofibromatosis', 'XPO:0141783', 'abnormal collagen metabolic process', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(406499, 'HP:0020135', 'Myofibromatosis', 'XPO:0100232', 'abnormal lymphatic system', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(406500, 'HP:0020135', 'Myofibromatosis', 'XPO:0100308', 'abnormal early embryonic cell', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(406501, 'HP:0020135', 'Myofibromatosis', 'XPO:0101264', 'abnormal mitotic spindle', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(406502, 'HP:0020135', 'Myofibromatosis', 'XPO:0100481', 'abnormal anatomical line', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406503, 'HP:0020135', 'Myofibromatosis', 'XPO:0100004', 'abnormal cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(406504, 'HP:0020135', 'Myofibromatosis', 'XPO:0100307', 'abnormal blastomere', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(406505, 'HP:0020135', 'Myofibromatosis', 'XPO:0101547', 'abnormal lampbrush chromosome', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(406506, 'HP:0020135', 'Myofibromatosis', 'XPO:0141782', 'abnormal methylation', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(406507, 'HP:0020135', 'Myofibromatosis', 'XPO:0100006', 'abnormal anatomical structure', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406508, 'HP:0020135', 'Myofibromatosis', 'XPO:0141272', 'absent surface breathing', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406509, 'HP:0020135', 'Myofibromatosis', 'XPO:0141892', 'abnormal inositol metabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(406510, 'HP:0020135', 'Myofibromatosis', 'XPO:0141776', 'abnormal metabolic process', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(406511, 'HP:0020135', 'Myofibromatosis', 'XPO:0131745', 'abnormal axis elongation', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(406512, 'HP:0020135', 'Myofibromatosis', 'XPO:0142057', 'abnormal desmosome', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(406513, 'HP:0020135', 'Myofibromatosis', 'XPO:0100585', 'abnormal elastica externa', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(406514, 'HP:0020135', 'Myofibromatosis', 'XPO:0100372', 'abnormal hematological system', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(406515, 'HP:0020135', 'Myofibromatosis', 'XPO:0100626', 'abnormal primordial germ cell', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(406516, 'HP:0020135', 'Myofibromatosis', 'XPO:0100344', 'abnormal portion of organism substance', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406517, 'HP:0020135', 'Myofibromatosis', 'XPO:0101377', 'abnormal manicotto glandulare', 0.46153846153846156, 4.970960464763942, 1.5146912045944103, 'HP:0011793', 'Neoplasm by anatomical site'),
(406518, 'HP:0020135', 'Myofibromatosis', 'XPO:0141264', 'abnormal schooling behavior', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406519, 'HP:0020135', 'Myofibromatosis', 'XPO:0100108', 'abnormal cell part', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(406520, 'HP:0020135', 'Myofibromatosis', 'XPO:0100501', 'abnormal urogenital system', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(406521, 'HP:0020135', 'Myofibromatosis', 'XPO:0100704', 'abnormal Merkel cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(406522, 'HP:0020135', 'Myofibromatosis', 'XPO:0131730', 'abnormal regulation of protein folding', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406523, 'HP:0020135', 'Myofibromatosis', 'XPO:0101381', 'abnormal ventral foregut', 0.4444444444444444, 4.970960464763942, 1.4863767228119886, 'HP:0011793', 'Neoplasm by anatomical site'),
(406524, 'HP:0020135', 'Myofibromatosis', 'XPO:0141775', 'abnormal nitrogen compound metabolic process', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(406525, 'HP:0020135', 'Myofibromatosis', 'XPO:0141754', 'abnormal homeostatic process', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406526, 'HP:0020135', 'Myofibromatosis', 'XPO:0141748', 'abnormal gas homeostasis', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406527, 'HP:0020135', 'Myofibromatosis', 'XPO:0100728', 'abnormal cell condensation', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406528, 'HP:0020135', 'Myofibromatosis', 'XPO:0101141', 'abnormal Keller explant', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406529, 'HP:0020135', 'Myofibromatosis', 'XPO:0128000', 'absent behavior', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406530, 'HP:0020135', 'Myofibromatosis', 'XPO:0100176', 'abnormal stage VI oocyte', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(406531, 'HP:0020135', 'Myofibromatosis', 'XPO:0101480', 'abnormal stage V oocyte', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(406532, 'HP:0020135', 'Myofibromatosis', 'XPO:0100976', 'abnormal multiciliated cell', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(406533, 'HP:0020135', 'Myofibromatosis', 'XPO:0100337', 'abnormal zygote', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(406534, 'HP:0020135', 'Myofibromatosis', 'XPO:0101535', 'abnormal absorptive cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(406535, 'HP:0020135', 'Myofibromatosis', 'XPO:0101110', 'abnormal cell-free extract', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406536, 'HP:0020135', 'Myofibromatosis', 'XPO:0141267', 'abnormal resting posture', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406537, 'HP:0020135', 'Myofibromatosis', 'XPO:0141904', 'abnormal glucosamine metabolic process', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(406538, 'HP:0020135', 'Myofibromatosis', 'XPO:0101240', 'abnormal ciliated non-epidermal cell', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(406539, 'HP:0020135', 'Myofibromatosis', 'XPO:0101113', 'abnormal stage IV oocyte', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(406540, 'HP:0002878', 'Respiratory failure', 'XPO:0100804', 'abnormal larynx', 0.4186046511627907, 7.032762738978795, 1.7157934587417247, 'HP:0002795', 'Abnormal respiratory system physiology'),
(406541, 'HP:0002878', 'Respiratory failure', 'XPO:0139850', 'abnormally necrotic respiratory system', 0.4186046511627907, 7.032762738978795, 1.7157934587417247, 'UPHENO:0002448', 'abnormality of respiratory system physiology'),
(406542, 'HP:0002878', 'Respiratory failure', 'XPO:0101949', 'abnormal respiratory system morphology', 0.47368421052631576, 7.032762738978795, 1.825187296096502, 'HP:0002795', 'Abnormal respiratory system physiology'),
(406543, 'HP:0002878', 'Respiratory failure', 'XPO:0101543', 'abnormal external gill', 0.40625, 6.780552239366747, 1.6596985711998251, 'UPHENO:0004536', 'abnormal respiratory system'),
(406544, 'HP:0002878', 'Respiratory failure', 'XPO:0100317', 'abnormal respiratory system', 0.4642857142857143, 6.780552239366747, 1.7742924053565663, 'UPHENO:0004536', 'abnormal respiratory system'),
(406545, 'HP:0002810', 'Dumbbell-shaped metaphyses', 'XPO:0100178', 'abnormal digit', 0.43333333333333335, 5.802924133159483, 1.5857491786857223, 'UPHENO:0076727', 'abnormal limb bone morphology'),
(406546, 'HP:0002810', 'Dumbbell-shaped metaphyses', 'XPO:0101810', 'abnormal digit morphology', 0.42028985507246375, 5.802924133159483, 1.561701041467957, 'UPHENO:0076727', 'abnormal limb bone morphology'),
(406547, 'HP:0002810', 'Dumbbell-shaped metaphyses', 'XPO:0101248', 'abnormal digit-joint region', 0.4126984126984127, 5.802924133159483, 1.547532739157473, 'UPHENO:0076727', 'abnormal limb bone morphology'),
(406548, 'HP:0002810', 'Dumbbell-shaped metaphyses', 'XPO:0102880', 'abnormal digit-joint region morphology', 0.42028985507246375, 5.802924133159483, 1.561701041467957, 'UPHENO:0076727', 'abnormal limb bone morphology'),
(406549, 'HP:0034450', 'Decreased phytanic acid:pristanic acid ratio', 'XPO:0141887', 'abnormal histidine metabolic process', 0.5294117647058824, 9.119292702704945, 2.1972393685278124, 'HP:0004354', 'Abnormal circulating carboxylic acid concentration'),
(406550, 'HP:0034450', 'Decreased phytanic acid:pristanic acid ratio', 'XPO:0141869', 'abnormal alpha-amino acid metabolic process', 0.5538461538461539, 9.119292702704945, 2.2473729528474866, 'HP:0004354', 'Abnormal circulating carboxylic acid concentration'),
(406551, 'HP:0034450', 'Decreased phytanic acid:pristanic acid ratio', 'XPO:0141882', 'abnormal gamma-aminobutyric acid metabolic process', 0.5692307692307692, 10.553838360873003, 2.4510343792972265, 'UPHENO:0050484', 'abnormal monocarboxylic acid metabolic process'),
(406552, 'HP:0034450', 'Decreased phytanic acid:pristanic acid ratio', 'XPO:0141843', 'abnormal alanine metabolic process', 0.5373134328358209, 9.119292702704945, 2.2135759456420385, 'HP:0004354', 'Abnormal circulating carboxylic acid concentration'),
(406553, 'HP:0034450', 'Decreased phytanic acid:pristanic acid ratio', 'XPO:0141889', 'abnormal homoserine metabolic process', 0.5217391304347826, 9.119292702704945, 2.1812592337660224, 'HP:0004354', 'Abnormal circulating carboxylic acid concentration'),
(406554, 'HP:0034450', 'Decreased phytanic acid:pristanic acid ratio', 'XPO:0141917', 'abnormal tryptophan metabolic process', 0.5294117647058824, 9.119292702704945, 2.1972393685278124, 'HP:0004354', 'Abnormal circulating carboxylic acid concentration'),
(406555, 'HP:0034450', 'Decreased phytanic acid:pristanic acid ratio', 'XPO:0141847', 'abnormal arginine metabolic process', 0.5294117647058824, 9.119292702704945, 2.1972393685278124, 'HP:0004354', 'Abnormal circulating carboxylic acid concentration'),
(406556, 'HP:0034450', 'Decreased phytanic acid:pristanic acid ratio', 'XPO:0141853', 'abnormal glutamate metabolic process', 0.5142857142857142, 9.119292702704945, 2.1656227652550926, 'HP:0004354', 'Abnormal circulating carboxylic acid concentration'),
(406557, 'HP:0034450', 'Decreased phytanic acid:pristanic acid ratio', 'XPO:0141922', 'abnormal valine metabolic process', 0.5294117647058824, 9.119292702704945, 2.1972393685278124, 'HP:0004354', 'Abnormal circulating carboxylic acid concentration'),
(406558, 'HP:0034450', 'Decreased phytanic acid:pristanic acid ratio', 'XPO:0141868', 'abnormal asparagine metabolic process', 0.5294117647058824, 9.119292702704945, 2.1972393685278124, 'HP:0004354', 'Abnormal circulating carboxylic acid concentration'),
(406559, 'HP:0034450', 'Decreased phytanic acid:pristanic acid ratio', 'XPO:0141893', 'abnormal isoleucine metabolic process', 0.5294117647058824, 9.119292702704945, 2.1972393685278124, 'HP:0004354', 'Abnormal circulating carboxylic acid concentration'),
(406560, 'HP:0034450', 'Decreased phytanic acid:pristanic acid ratio', 'XPO:0141896', 'abnormal lysine metabolic process', 0.5294117647058824, 9.119292702704945, 2.1972393685278124, 'HP:0004354', 'Abnormal circulating carboxylic acid concentration'),
(406561, 'HP:0034450', 'Decreased phytanic acid:pristanic acid ratio', 'XPO:0141873', 'abnormal tricarboxylic acid metabolic process', 0.5645161290322581, 9.119292702704945, 2.2689177631732522, 'HP:0004354', 'Abnormal circulating carboxylic acid concentration'),
(406562, 'HP:0034450', 'Decreased phytanic acid:pristanic acid ratio', 'XPO:0141918', 'abnormal tyrosine metabolic process', 0.5294117647058824, 9.119292702704945, 2.1972393685278124, 'HP:0004354', 'Abnormal circulating carboxylic acid concentration'),
(406563, 'HP:0034450', 'Decreased phytanic acid:pristanic acid ratio', 'XPO:0141858', 'abnormal serine family amino acid metabolic process', 0.5373134328358209, 9.119292702704945, 2.2135759456420385, 'HP:0004354', 'Abnormal circulating carboxylic acid concentration'),
(406564, 'HP:0034450', 'Decreased phytanic acid:pristanic acid ratio', 'XPO:0141857', 'abnormal glycine metabolic process', 0.5217391304347826, 9.119292702704945, 2.1812592337660224, 'HP:0004354', 'Abnormal circulating carboxylic acid concentration'),
(406565, 'HP:0034450', 'Decreased phytanic acid:pristanic acid ratio', 'XPO:0141848', 'abnormal proline metabolic process', 0.5294117647058824, 9.119292702704945, 2.1972393685278124, 'HP:0004354', 'Abnormal circulating carboxylic acid concentration'),
(406566, 'HP:0034450', 'Decreased phytanic acid:pristanic acid ratio', 'XPO:0141912', 'abnormal D-serine metabolic process', 0.5217391304347826, 9.119292702704945, 2.1812592337660224, 'HP:0004354', 'Abnormal circulating carboxylic acid concentration'),
(406567, 'HP:0034450', 'Decreased phytanic acid:pristanic acid ratio', 'XPO:0141905', 'abnormal ornithine metabolic process', 0.5373134328358209, 9.119292702704945, 2.2135759456420385, 'HP:0004354', 'Abnormal circulating carboxylic acid concentration'),
(406568, 'HP:0034450', 'Decreased phytanic acid:pristanic acid ratio', 'XPO:0141913', 'abnormal L-serine metabolic process', 0.5217391304347826, 9.119292702704945, 2.1812592337660224, 'HP:0004354', 'Abnormal circulating carboxylic acid concentration'),
(406569, 'HP:0034450', 'Decreased phytanic acid:pristanic acid ratio', 'XPO:0141895', 'abnormal leucine metabolic process', 0.5294117647058824, 9.119292702704945, 2.1972393685278124, 'HP:0004354', 'Abnormal circulating carboxylic acid concentration'),
(406570, 'HP:0034450', 'Decreased phytanic acid:pristanic acid ratio', 'XPO:0141888', 'abnormal threonine metabolic process', 0.5294117647058824, 9.119292702704945, 2.1972393685278124, 'HP:0004354', 'Abnormal circulating carboxylic acid concentration'),
(406571, 'HP:0032228', 'Trichodiscoma', 'XPO:0101740', 'abnormal cell part morphology', 0.4166666666666667, 2.786899518863159, 1.0775936770692605, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(406572, 'HP:0032228', 'Trichodiscoma', 'XPO:0101713', 'abnormal anatomical entity in vitro morphology', 0.43333333333333335, 2.786899518863159, 1.0989342374200721, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(406573, 'HP:0032228', 'Trichodiscoma', 'XPO:0102773', 'abnormal Keller explant morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(406574, 'HP:0032228', 'Trichodiscoma', 'XPO:0102626', 'abnormal granular gland morphology', 0.40425531914893614, 6.8660902472206855, 1.6660292627068698, 'HP:0000951', 'Abnormality of the skin'),
(406575, 'HP:0032228', 'Trichodiscoma', 'XPO:0101784', 'abnormal alimentary system morphology', 0.4146341463414634, 4.970960464763942, 1.4356635917945963, 'HP:0011793', 'Neoplasm by anatomical site'),
(406576, 'HP:0032228', 'Trichodiscoma', 'XPO:0101636', 'abnormal cell morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(406577, 'HP:0032228', 'Trichodiscoma', 'XPO:0107345', 'abnormal anatomical axis morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(406578, 'HP:0032228', 'Trichodiscoma', 'XPO:0102522', 'abnormal pharyngeal cavity morphology', 0.4146341463414634, 4.970960464763942, 1.4356635917945963, 'HP:0011793', 'Neoplasm by anatomical site'),
(406579, 'HP:0032228', 'Trichodiscoma', 'XPO:0102727', 'abnormal skin seromucous gland morphology', 0.40425531914893614, 6.8660902472206855, 1.6660292627068698, 'HP:0000951', 'Abnormality of the skin'),
(406580, 'HP:0032228', 'Trichodiscoma', 'XPO:0102139', 'abnormal skin morphology', 0.4222222222222222, 6.8660902472206855, 1.7026496651278105, 'HP:0000951', 'Abnormality of the skin'),
(406581, 'HP:0032228', 'Trichodiscoma', 'XPO:0102561', 'abnormal dermis morphology', 0.41304347826086957, 6.8660902472206855, 1.6840409133287308, 'HP:0000951', 'Abnormality of the skin'),
(406582, 'HP:0032228', 'Trichodiscoma', 'XPO:0102113', 'abnormal anatomical line morphology', 0.43333333333333335, 2.786899518863159, 1.0989342374200721, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(406583, 'HP:0032228', 'Trichodiscoma', 'XPO:0102601', 'abnormal disaggregated/reaggregated ectoderm treated with activin morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(406584, 'HP:0032228', 'Trichodiscoma', 'XPO:0101694', 'abnormal anatomical space morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(406585, 'HP:0032228', 'Trichodiscoma', 'XPO:0101976', 'abnormal portion of organism substance morphology', 0.43333333333333335, 2.786899518863159, 1.0989342374200721, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(406586, 'HP:0032228', 'Trichodiscoma', 'XPO:0102615', 'abnormal skin gland morphology', 0.4222222222222222, 6.8660902472206855, 1.7026496651278105, 'HP:0000951', 'Abnormality of the skin'),
(406587, 'HP:0032228', 'Trichodiscoma', 'XPO:0140144', 'abnormally necrotic portion of organism substance', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(406588, 'HP:0032228', 'Trichodiscoma', 'XPO:0102742', 'abnormal cell-free extract morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(406589, 'HP:0032228', 'Trichodiscoma', 'XPO:0141316', 'abnormal anatomical region morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(406590, 'HP:0032228', 'Trichodiscoma', 'XPO:0103201', 'abnormal activin-induced ectoderm morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(406591, 'HP:0032228', 'Trichodiscoma', 'XPO:0100507', 'abnormal skin', 0.40540540540540543, 6.8660902472206855, 1.6683974647021622, 'HP:0000951', 'Abnormality of the skin'),
(406592, 'HP:0032228', 'Trichodiscoma', 'XPO:0140269', 'abnormally necrotic anatomical line', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(406593, 'HP:0032228', 'Trichodiscoma', 'XPO:0101638', 'abnormal anatomical structure morphology', 0.43333333333333335, 2.786899518863159, 1.0989342374200721, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(406594, 'HP:0032228', 'Trichodiscoma', 'XPO:0102178', 'abnormal whole organism morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(406595, 'HP:0032228', 'Trichodiscoma', 'XPO:0101890', 'abnormal organ part morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(406596, 'HP:0032228', 'Trichodiscoma', 'XPO:0115392', 'abnormally incomplete structure of alimentary system', 0.40476190476190477, 4.970960464763942, 1.4184693955859522, 'HP:0011793', 'Neoplasm by anatomical site'),
(406597, 'HP:0032228', 'Trichodiscoma', 'XPO:0139718', 'abnormally necrotic anatomical structure', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(406598, 'HP:0012626', 'Stage 4 chronic kidney disease', 'XPO:0100147', 'abnormal mesonephric mesenchyme', 0.4523809523809524, 6.880013295263146, 1.76419584142599, 'HP:0000077', 'Abnormality of the kidney'),
(406599, 'HP:0012626', 'Stage 4 chronic kidney disease', 'XPO:0107300', 'abnormal embryonic kidney', 0.4318181818181818, 6.880013295263146, 1.7236341932224046, 'HP:0000077', 'Abnormality of the kidney'),
(406600, 'HP:0012626', 'Stage 4 chronic kidney disease', 'XPO:0126072', 'absent mesonephric sinus', 0.40816326530612246, 6.880013295263146, 1.6757591390006326, 'HP:0000077', 'Abnormality of the kidney'),
(406601, 'HP:0012626', 'Stage 4 chronic kidney disease', 'XPO:0127733', 'abnormally localised mesonephric sinus', 0.4444444444444444, 6.880013295263146, 1.7486519627369022, 'HP:0000077', 'Abnormality of the kidney'),
(406602, 'HP:0012626', 'Stage 4 chronic kidney disease', 'XPO:0101717', 'abnormal mesonephric sinus morphology', 0.4166666666666667, 6.880013295263146, 1.6931249824982337, 'HP:0000077', 'Abnormality of the kidney'),
(406603, 'HP:0012626', 'Stage 4 chronic kidney disease', 'XPO:0107301', 'abnormal adult kidney', 0.4318181818181818, 6.880013295263146, 1.7236341932224046, 'HP:0000077', 'Abnormality of the kidney'),
(406604, 'HP:0012626', 'Stage 4 chronic kidney disease', 'XPO:0141613', 'metaplastic kidney', 0.43478260869565216, 6.880013295263146, 1.7295404384908961, 'HP:0000077', 'Abnormality of the kidney'),
(406605, 'HP:0012626', 'Stage 4 chronic kidney disease', 'XPO:0100085', 'abnormal mesonephric sinus', 0.48717948717948717, 6.880013295263146, 1.83079254667872, 'HP:0000077', 'Abnormality of the kidney'),
(406606, 'HP:0012626', 'Stage 4 chronic kidney disease', 'XPO:0100566', 'abnormal kidney', 0.4418604651162791, 6.880013295263146, 1.7435612620872136, 'HP:0000077', 'Abnormality of the kidney'),
(406607, 'HP:0009289', 'Aplasia/Hypoplasia of the distal phalanx of the 4th finger', 'XPO:0103282', 'absent forelimb digit 5', 0.41732283464566927, 10.200822588201543, 2.063258635805468, 'HP:0005927', 'Aplasia/hypoplasia involving bones of the hand'),
(406608, 'HP:0009289', 'Aplasia/Hypoplasia of the distal phalanx of the 4th finger', 'XPO:0102214', 'abnormal forelimb digit morphology', 0.42727272727272725, 7.492661022682715, 1.7892483644513149, 'HP:0001167', 'Abnormal finger morphology'),
(406609, 'HP:0009289', 'Aplasia/Hypoplasia of the distal phalanx of the 4th finger', 'XPO:0103279', 'absent forelimb digit 2', 0.41732283464566927, 10.200822588201543, 2.063258635805468, 'HP:0005927', 'Aplasia/hypoplasia involving bones of the hand'),
(406610, 'HP:0009289', 'Aplasia/Hypoplasia of the distal phalanx of the 4th finger', 'XPO:0103280', 'absent forelimb digit 3', 0.41732283464566927, 10.200822588201543, 2.063258635805468, 'HP:0005927', 'Aplasia/hypoplasia involving bones of the hand'),
(406611, 'HP:0009289', 'Aplasia/Hypoplasia of the distal phalanx of the 4th finger', 'XPO:0103609', 'abnormally increased number of forelimb digit in the regenerating forelimb', 0.4418604651162791, 7.774297771301195, 1.8534170683307085, 'HP:0005918', 'Abnormal finger phalanx morphology'),
(406612, 'HP:0009289', 'Aplasia/Hypoplasia of the distal phalanx of the 4th finger', 'XPO:0115786', 'duplicated forelimb digit 2 in regenerating forelimb', 0.4253731343283582, 7.774297771301195, 1.8185096673321148, 'HP:0005918', 'Abnormal finger phalanx morphology'),
(406613, 'HP:0009289', 'Aplasia/Hypoplasia of the distal phalanx of the 4th finger', 'XPO:0103281', 'absent forelimb digit 4', 0.41732283464566927, 10.200822588201543, 2.063258635805468, 'HP:0005927', 'Aplasia/hypoplasia involving bones of the hand'),
(406614, 'HP:0009289', 'Aplasia/Hypoplasia of the distal phalanx of the 4th finger', 'XPO:0115789', 'duplicated forelimb digit 5 in regenerating forelimb', 0.4253731343283582, 7.774297771301195, 1.8185096673321148, 'HP:0005918', 'Abnormal finger phalanx morphology'),
(406615, 'HP:0009289', 'Aplasia/Hypoplasia of the distal phalanx of the 4th finger', 'XPO:0141556', 'abnormal forelimb digit morphology in the regenerating forelimb', 0.4051724137931034, 7.492661022682715, 1.7423603393941962, 'HP:0001167', 'Abnormal finger morphology'),
(406616, 'HP:0009289', 'Aplasia/Hypoplasia of the distal phalanx of the 4th finger', 'XPO:0103634', 'abnormally increased number of forelimb digit', 0.4634146341463415, 7.774297771301195, 1.8980841281229506, 'HP:0005918', 'Abnormal finger phalanx morphology'),
(406617, 'HP:0009289', 'Aplasia/Hypoplasia of the distal phalanx of the 4th finger', 'XPO:0102529', 'abnormal forelimb digit 4 morphology', 0.41964285714285715, 7.492661022682715, 1.7732009697610411, 'HP:0001167', 'Abnormal finger morphology'),
(406618, 'HP:0009289', 'Aplasia/Hypoplasia of the distal phalanx of the 4th finger', 'XPO:0115787', 'duplicated forelimb digit 3 in regenerating forelimb', 0.4253731343283582, 7.774297771301195, 1.8185096673321148, 'HP:0005918', 'Abnormal finger phalanx morphology'),
(406619, 'HP:0009289', 'Aplasia/Hypoplasia of the distal phalanx of the 4th finger', 'XPO:0102598', 'abnormal forelimb digit 3 morphology', 0.41964285714285715, 7.492661022682715, 1.7732009697610411, 'HP:0001167', 'Abnormal finger morphology'),
(406620, 'HP:0009289', 'Aplasia/Hypoplasia of the distal phalanx of the 4th finger', 'XPO:0102787', 'abnormal forelimb digit 5 morphology', 0.41964285714285715, 7.492661022682715, 1.7732009697610411, 'HP:0001167', 'Abnormal finger morphology'),
(406621, 'HP:0009289', 'Aplasia/Hypoplasia of the distal phalanx of the 4th finger', 'XPO:0125257', 'absent forelimb digit', 0.4274193548387097, 10.200822588201543, 2.0880682482795527, 'HP:0005927', 'Aplasia/hypoplasia involving bones of the hand'),
(406622, 'HP:0009289', 'Aplasia/Hypoplasia of the distal phalanx of the 4th finger', 'XPO:0115788', 'duplicated forelimb digit 4 in regenerating forelimb', 0.4253731343283582, 7.774297771301195, 1.8185096673321148, 'HP:0005918', 'Abnormal finger phalanx morphology'),
(406623, 'HP:0009289', 'Aplasia/Hypoplasia of the distal phalanx of the 4th finger', 'XPO:0102746', 'abnormal forelimb digit 2 morphology', 0.41964285714285715, 7.492661022682715, 1.7732009697610411, 'HP:0001167', 'Abnormal finger morphology'),
(406624, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0101405', 'abnormal ring structure', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(406625, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0100422', 'abnormal notochord', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(406626, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0141772', 'abnormal water homeostasis', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406627, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0100289', 'abnormal chondroblast', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(406628, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0107263', 'abnormal anatomical side', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406629, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0100969', 'abnormal disaggregated/reaggregated ectoderm treated with activin', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406630, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0131744', 'abnormal apical constriction', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406631, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0100907', 'abnormal cytoplasm', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(406632, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0100307', 'abnormal blastomere', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(406633, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0100587', 'abnormal vestibuloauditory system', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(406634, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0141920', 'abnormal urea metabolic process', 0.4074074074074074, 4.758907843651163, 1.392413123563799, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(406635, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0100956', 'abnormal centrosome', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(406636, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0131725', 'abnormal phosphorylation of RNA polymerase II C-terminal domain', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406637, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0141315', 'abnormal anatomical region', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406638, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0131669', 'abnormal Roux spot', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(406639, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0100205', 'abnormal limb segment', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(406640, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0141859', 'abnormal lactose catabolic process', 0.44, 4.758907843651163, 1.447038165082909, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(406641, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0100547', 'abnormal blastomere V2', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(406642, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0141782', 'abnormal methylation', 0.55, 4.758907843651163, 1.6178378515809735, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(406643, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0100202', 'abnormal embryo', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406644, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0100888', 'abnormal microtubule', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(406645, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0141792', 'abnormal small molecule metabolic process', 0.55, 4.758907843651163, 1.6178378515809735, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(406646, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0141904', 'abnormal glucosamine metabolic process', 0.55, 4.758907843651163, 1.6178378515809735, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(406647, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0100031', 'abnormal central nervous system', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(406648, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0131687', 'abnormal astral microtubule', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(406649, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:00000000', 'Xenopus phenotype', 0.5714285714285714, 1.4755025719078136, 0.918228907628411, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406650, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0100545', 'abnormal male organism', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406651, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0107273', 'abnormal basal region', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406652, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0101240', 'abnormal ciliated non-epidermal cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(406653, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0100258', 'abnormal organ part', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406654, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0101157', 'abnormal female organism', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406655, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0141767', 'abnormal temperature homeostasis', 0.4583333333333333, 4.758907843651163, 1.4768771428276568, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(406656, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0100762', 'abnormal intersomitic region', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406657, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0141960', 'absent cilium motility in brain', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406658, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0100437', 'abnormal proepicardium', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(406659, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0116433', 'abnormal axis specification', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406660, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0141898', 'abnormal maltose metabolic process', 0.4782608695652174, 4.758907843651163, 1.508641575552437, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(406661, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0141900', 'abnormal mannose metabolic process', 0.44, 4.758907843651163, 1.447038165082909, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(406662, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0116494', 'absent biological process', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406663, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0141864', 'abnormal 5-methylcytosine metabolic process', 0.44, 4.758907843651163, 1.447038165082909, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(406664, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0107272', 'abnormal axial region', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406665, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0107262', 'abnormal left-right axis', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406666, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0100277', 'abnormal blastocoel', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406667, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0107261', 'abnormal dorsal-ventral axis', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406668, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0141860', 'abnormal malate-aspartate shuttle', 0.5238095238095238, 4.758907843651163, 1.5788480773767701, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(406669, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0141964', 'absent cilium motility in olfactory pit', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406670, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0107270', 'abnormal proximal-distal axis', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406671, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0100372', 'abnormal hematological system', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(406672, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0100477', 'abnormal pericyte', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(406673, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0100081', 'abnormal anatomical entity in vitro', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406674, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0141884', 'abnormal phosphagen metabolic process', 0.44, 4.758907843651163, 1.447038165082909, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(406675, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0100104', 'abnormal embryonic structure', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406676, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0101200', 'abnormal joint region', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406677, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0101472', 'abnormal zygote cortex', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(406678, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0100028', 'abnormal anatomical cluster', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406679, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0100032', 'abnormal nervous system', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(406680, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0141754', 'abnormal homeostatic process', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406681, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0141908', 'abnormal pyridine metabolic process', 0.44, 4.758907843651163, 1.447038165082909, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(406682, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0141789', 'abnormal hormone catabolic process', 0.4583333333333333, 4.758907843651163, 1.4768771428276568, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(406683, 'HP:0012309', 'Cutaneous amyloidosis', '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'),
(406684, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0100721', 'abnormal centromere', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(406685, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0116434', 'abnormal biological process', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406686, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0101435', 'abnormal paracrine cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(406687, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0141892', 'abnormal inositol metabolic process', 0.5, 4.758907843651163, 1.5425478669479211, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(406688, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0141790', 'abnormal cellular metabolic process', 0.5238095238095238, 4.758907843651163, 1.5788480773767701, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(406689, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0100317', 'abnormal respiratory system', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(406690, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0100574', 'abnormal gastrula cell', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(406691, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0101297', 'abnormal barrier cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(406692, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0141775', 'abnormal nitrogen compound metabolic process', 0.55, 4.758907843651163, 1.6178378515809735, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(406693, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0100337', 'abnormal zygote', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(406694, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0100653', 'abnormal myoblast', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(406695, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0141272', 'absent surface breathing', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406696, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0131667', 'abnormal actin cytoskeleton', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(406697, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0131677', 'abnormal actin filament', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(406698, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0131740', 'abnormal detection of nodal flow', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406699, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0100546', 'abnormal whole organism', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406700, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0141784', 'abnormal cellular hormone metabolic process', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406701, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0100218', 'abnormal epithelial cell', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(406702, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0100225', 'abnormal endocrine system', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(406703, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0141899', 'abnormal mandelate metabolic process', 0.4074074074074074, 4.758907843651163, 1.392413123563799, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(406704, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0101110', 'abnormal cell-free extract', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406705, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0101411', 'abnormal marginal zone (sensu neural)', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406706, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0101409', 'abnormal perivitelline space', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(406707, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0131675', 'abnormal spindle microtubule', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(406708, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0115509', 'abnormally semi-viable whole organism', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406709, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0100239', 'abnormal acellular anatomical structure', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406710, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0100006', 'abnormal anatomical structure', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406711, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0101333', 'abnormal barrier epithelial cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(406712, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0141791', 'abnormal primary metabolic process', 0.55, 4.758907843651163, 1.6178378515809735, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(406713, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0141852', 'abnormal glucose metabolic process', 0.44, 4.758907843651163, 1.447038165082909, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(406714, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0141872', 'abnormal cholesterol metabolic process', 0.4230769230769231, 4.758907843651163, 1.418937661667548, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(406715, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0141778', 'abnormal biosynthetic process', 0.55, 4.758907843651163, 1.6178378515809735, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(406716, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0101113', 'abnormal stage IV oocyte', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(406717, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0100626', 'abnormal primordial germ cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(406718, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0100902', 'abnormal spermatocyte', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(406719, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0100862', 'abnormal blastomere V1', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(406720, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0100429', 'abnormal spermatid', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(406721, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0100010', 'abnormal multicellular anatomical structure', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406722, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0100465', 'abnormal skeletal system', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(406723, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0107276', 'abnormal dorsal region', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406724, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0100176', 'abnormal stage VI oocyte', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(406725, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0107339', 'abnormal yolk platelet', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(406726, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0101497', 'abnormal ciliary axoneme', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(406727, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0100172', 'abnormal stem cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(406728, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0101366', 'abnormal morula cell', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(406729, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0100842', 'abnormal left-dorsal blastomere', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(406730, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0101570', 'abnormal forelimb region', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406731, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0141263', 'abnormal visually guided collision avoidance behavior', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406732, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0101311', 'abnormal bottle cell', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(406733, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0101389', 'abnormal wedge region', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(406734, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0100273', 'abnormal visual system', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(406735, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0100295', 'abnormal extracellular matrix', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406736, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0100674', 'abnormal secondary oogonium', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(406737, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0100899', 'abnormal secondary spermatogonium', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(406738, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0100599', 'abnormal adult immune system', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(406739, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0141856', 'abnormal glycerolipid metabolic process', 0.4074074074074074, 4.758907843651163, 1.392413123563799, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(406740, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0131694', 'abnormal RNA polymerase II activity', 0.4782608695652174, 4.758907843651163, 1.508641575552437, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(406741, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0101373', 'abnormal oxygen accumulating cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(406742, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0141724', 'abnormal prevention of polyspermy', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406743, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0100386', 'abnormal limb', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(406744, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0141795', 'abnormal glycosylation', 0.5, 4.758907843651163, 1.5425478669479211, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(406745, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0100643', 'abnormal thoracic region', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406746, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0141786', 'abnormal pigment metabolic process', 0.55, 4.758907843651163, 1.6178378515809735, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(406747, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0115512', 'abnormally semi-erect whole organism', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406748, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0141962', 'absent cilium motility in pronephric kidney', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406749, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0131729', 'abnormal regulation of growth rate', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406750, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0115508', 'abnormally peramorphic growth of whole organism', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406751, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0141959', 'absent cilium motility in floor plate', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406752, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0101451', 'abnormal dorsal lymph space', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(406753, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0141880', 'abnormal ethanolamine metabolic process', 0.4583333333333333, 4.758907843651163, 1.4768771428276568, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(406754, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0100823', 'abnormal blood', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(406755, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0100852', 'abnormal interdigital region', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(406756, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0100802', 'abnormal exocrine cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(406757, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0141874', 'abnormal creatinine metabolic process', 0.4074074074074074, 4.758907843651163, 1.392413123563799, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(406758, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0101513', 'abnormal basal body', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(406759, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0101461', 'abnormal sperm entry point', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(406760, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0100014', 'abnormal tissue', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406761, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0141266', 'abnormal surface breathing', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406762, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0100025', 'abnormal oocyte', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(406763, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0107260', 'abnormal anterior-posterior axis', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406764, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0100344', 'abnormal portion of organism substance', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406765, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0141788', 'abnormal hormone biosynthetic process', 0.4583333333333333, 4.758907843651163, 1.4768771428276568, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(406766, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0100108', 'abnormal cell part', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(406767, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0100009', 'abnormal multi-tissue structure', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406768, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0100062', 'abnormal anatomical space', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406769, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0101132', 'abnormal apoptotic cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(406770, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0131723', 'abnormal pathway-restricted SMAD protein phosphorylation', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406771, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0131691', 'abnormal molecular function', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406772, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0101467', 'abnormal alkali secreting cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(406773, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0100791', 'abnormal multiciliated cell precursor', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(406774, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0100887', 'abnormal right-dorsal blastomere', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(406775, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0101136', 'abnormal ooplasm', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(406776, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0101141', 'abnormal Keller explant', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406777, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0141787', 'abnormal hormone metabolic process', 0.55, 4.758907843651163, 1.6178378515809735, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(406778, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0131666', 'abnormal adherens junction', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(406779, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0100784', 'abnormal left blastomere', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(406780, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0141785', 'abnormal thyroid hormone metabolic process', 0.4074074074074074, 4.758907843651163, 1.392413123563799, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(406781, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0100691', 'abnormal keratin accumulating cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(406782, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0101220', 'abnormal centriole', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(406783, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0101448', 'abnormal myelin accumulating cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(406784, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0133340', 'abnormal cell adhesion', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406785, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0141854', 'abnormal glutathione metabolic process', 0.44, 4.758907843651163, 1.447038165082909, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(406786, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0101575', 'abnormal vitelline membrane', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(406787, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0128000', 'absent behavior', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406788, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0100976', 'abnormal multiciliated cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(406789, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0141276', 'decreased surface breathing', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406790, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0100917', 'abnormal stage III oocyte', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(406791, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0141771', 'abnormal urea homeostasis', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406792, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0100285', 'abnormal progenitor cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(406793, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0100581', 'abnormal immune system', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(406794, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0131685', 'abnormal cortical actin cytoskeleton', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(406795, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0100688', 'abnormal adipose tissue', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(406796, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0133403', 'abnormal developmental process', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406797, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0100481', 'abnormal anatomical line', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406798, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0141499', 'abnormal tadpole', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406799, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0100728', 'abnormal cell condensation', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406800, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0100585', 'abnormal elastica externa', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(406801, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0107258', 'abnormal anatomical axis', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406802, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0141883', 'abnormal glycerol metabolic process', 0.44, 4.758907843651163, 1.447038165082909, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(406803, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0141783', 'abnormal collagen metabolic process', 0.55, 4.758907843651163, 1.6178378515809735, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(406804, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0100894', 'abnormal nucleus', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(406805, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0141911', 'abnormal ribose phosphate metabolic process', 0.4782608695652174, 4.758907843651163, 1.508641575552437, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(406806, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0100989', 'abnormal right blastomere', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(406807, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0131469', 'abnormal heart process', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406808, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0100573', 'abnormal extraembryonic structure', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406809, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0141796', 'abnormal demethylation', 0.55, 4.758907843651163, 1.6178378515809735, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(406810, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0107312', 'abnormal filopodium', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(406811, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0100003', 'abnormal organism subdivision', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406812, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0100308', 'abnormal early embryonic cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(406813, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0141798', 'abnormal lipid metabolic process', 0.5, 4.758907843651163, 1.5425478669479211, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(406814, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0100417', 'abnormal dense regular connective tissue', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(406815, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0101241', 'abnormal nucleate erythrocyte', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(406816, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0141745', 'abnormal creatinine homeostasis', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406817, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0141770', 'abnormal urate homeostasis', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406818, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0100754', 'abnormal electrically active cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(406819, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0100533', 'abnormal melanoblast', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(406820, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0107253', 'abnormal enteric nervous system', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(406821, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0107259', 'abnormal animal-vegetal axis', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406822, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0100665', 'abnormal egg jelly', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406823, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0101569', 'abnormal activin-induced ectoderm', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406824, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0141958', 'absent cilium motility in left-right organizer', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406825, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0141271', 'increased surface breathing', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406826, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0101072', 'abnormal mitochondrial cloud', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(406827, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0101283', 'abnormal left-ventral blastomere', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(406828, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0141600', 'absent metamorphosis', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406829, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0142057', 'abnormal desmosome', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(406830, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0101302', 'abnormal subcortical cytoplasm', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(406831, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0141903', 'abnormal inositol phosphate metabolic process', 0.44, 4.758907843651163, 1.447038165082909, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(406832, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0141866', 'abnormal dicarboxylic acid metabolic process', 0.4230769230769231, 4.758907843651163, 1.418937661667548, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(406833, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0100004', 'abnormal cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(406834, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0101228', 'abnormal mesenchymal stem cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(406835, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0100070', 'abnormal anatomical system', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406836, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0101468', 'abnormal stage I oocyte', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(406837, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0141975', 'abnormal cilium motility', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406838, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0100427', 'abnormal olfactory system', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(406839, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0100423', 'abnormal process', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406840, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0141748', 'abnormal gas homeostasis', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406841, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0141738', 'abnormal carbon dioxide homeostasis', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406842, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0100503', 'abnormal blastomere D2', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(406843, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0131745', 'abnormal axis elongation', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(406844, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0101535', 'abnormal absorptive cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(406845, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0100515', 'abnormal somatic stem cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(406846, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0141910', 'abnormal D-ribose metabolic process', 0.44, 4.758907843651163, 1.447038165082909, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(406847, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0141777', 'abnormal catabolic process', 0.55, 4.758907843651163, 1.6178378515809735, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(406848, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0141794', 'abnormal prosthetic group metabolic process', 0.55, 4.758907843651163, 1.6178378515809735, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(406849, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0141809', 'abnormal catalytic activity', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406850, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0141877', 'abnormal 2-deoxyribose 1-phosphate metabolic process', 0.4782608695652174, 4.758907843651163, 1.508641575552437, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(406851, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0101498', 'abnormal stage II oocyte', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(406852, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0141762', 'abnormal multicellular organismal water homeostasis', 0.4074074074074074, 4.758907843651163, 1.392413123563799, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(406853, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0101378', 'abnormal blastomere D1', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(406854, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0100232', 'abnormal lymphatic system', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(406855, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0141907', 'abnormal putrescine metabolic process', 0.5, 4.758907843651163, 1.5425478669479211, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(406856, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0101326', 'abnormal cementoblast', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(406857, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0101071', 'abnormal endoplasmic reticulum', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(406858, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0141915', 'abnormal taurine metabolic process', 0.4074074074074074, 4.758907843651163, 1.392413123563799, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(406859, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0141264', 'abnormal schooling behavior', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406860, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0101347', 'abnormal hindlimb region', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406861, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0100715', 'abnormal ciliated cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(406862, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0100551', 'abnormal oocyte cortex', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(406863, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0100704', 'abnormal Merkel cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(406864, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0141863', 'abnormal lactate metabolic process', 0.4074074074074074, 4.758907843651163, 1.392413123563799, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(406865, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0101109', 'abnormal egg cell-free extract', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406866, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0100501', 'abnormal urogenital system', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(406867, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0107271', 'abnormal apical region', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406868, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0131730', 'abnormal regulation of protein folding', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406869, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0101004', 'abnormal acid secreting cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(406870, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0100642', 'abnormal gustatory system', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(406871, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0141850', 'abnormal galactose metabolic process', 0.44, 4.758907843651163, 1.447038165082909, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(406872, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0131722', 'abnormal determination of left/right symmetry', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406873, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0141781', 'abnormal secondary metabolic process', 0.55, 4.758907843651163, 1.6178378515809735, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(406874, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0100026', 'abnormal germ cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(406875, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0101547', 'abnormal lampbrush chromosome', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(406876, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0100724', 'abnormal kinetochore', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(406877, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0101463', 'abnormal right-ventral blastomere', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(406878, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0131719', 'abnormal activation of meiosis', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406879, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0141881', 'abnormal fructose metabolic process', 0.44, 4.758907843651163, 1.447038165082909, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(406880, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0100377', 'abnormal connective tissue', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(406881, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0100084', 'abnormal anatomical group', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406882, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0116429', 'abnormal behavior', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406883, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0100392', 'abnormal cilium', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(406884, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0100274', 'abnormal sensory system', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(406885, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0107278', 'abnormal medial region', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406886, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0141797', 'abnormal hydrogen metabolic process', 0.55, 4.758907843651163, 1.6178378515809735, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(406887, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0100152', 'abnormal alimentary system', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(406888, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0101061', 'abnormal plasma membrane', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(406889, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0141776', 'abnormal metabolic process', 0.6111111111111112, 4.758907843651163, 1.705350831943106, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(406890, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0141743', 'abnormal chemical homeostasis within a tissue', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406891, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0141265', 'abnormal escape behavior', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406892, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0115505', 'dead whole organism', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406893, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0133388', 'absent insulin receptor signaling pathway', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406894, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0100638', 'abnormal polar body', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(406895, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0101264', 'abnormal mitotic spindle', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(406896, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0101480', 'abnormal stage V oocyte', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(406897, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0107284', 'abnormal migrating myoblast', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(406898, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0100549', 'abnormal mitotic cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(406899, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0101221', 'abnormal larval immune system', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(406900, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0131703', 'abnormal cell division', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406901, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0141267', 'abnormal resting posture', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(406902, 'HP:0012309', 'Cutaneous amyloidosis', 'XPO:0101237', 'abnormal mucus secreting cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(406903, 'HP:0008251', 'Congenital goiter', 'XPO:0129055', 'decreased size of the thyroid', 0.48148148148148145, 11.627087342903641, 2.366057319503445, 'HP:0011772', 'Abnormal thyroid morphology'),
(406904, 'HP:0008251', 'Congenital goiter', 'XPO:0130401', 'increased size of the posterior region', 0.42105263157894735, 5.972749669260594, 1.585825326448175, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(406905, 'HP:0008251', 'Congenital goiter', 'XPO:0129982', 'increased size of the anatomical line', 0.45714285714285713, 5.972749669260594, 1.6523921595084028, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(406906, 'HP:0008251', 'Congenital goiter', 'XPO:0130304', 'increased size of the parathyroid', 0.4528301886792453, 7.767034997756375, 1.8754060689654177, 'UPHENO:0087376', 'abnormal endocrine gland morphology'),
(406907, 'HP:0008251', 'Congenital goiter', 'XPO:0130623', 'increased size of the ventro-lateral region', 0.42105263157894735, 5.972749669260594, 1.585825326448175, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(406908, 'HP:0008251', 'Congenital goiter', 'XPO:0129735', 'increased size of the endocrine system', 0.4888888888888889, 7.428233084304616, 1.9056706480904217, 'UPHENO:0076812', 'abnormal endocrine system morphology'),
(406909, 'HP:0008251', 'Congenital goiter', 'XPO:0128253', 'decreased size of the ultimobranchial body', 0.43137254901960786, 7.767034997756375, 1.830433196078642, 'UPHENO:0087376', 'abnormal endocrine gland morphology'),
(406910, 'HP:0008251', 'Congenital goiter', 'XPO:0129525', 'increased size of the anatomical group', 0.41025641025641024, 5.972749669260594, 1.565362206861726, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(406911, 'HP:0008251', 'Congenital goiter', 'XPO:0130769', 'increased size of the medial region', 0.41025641025641024, 5.972749669260594, 1.565362206861726, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(406912, 'HP:0008251', 'Congenital goiter', 'XPO:0102655', 'abnormal ultimobranchial body morphology', 0.4666666666666667, 7.767034997756375, 1.9038425177220695, 'UPHENO:0087376', 'abnormal endocrine gland morphology'),
(406913, 'HP:0008251', 'Congenital goiter', 'XPO:0129788', 'increased size of the organ part', 0.42105263157894735, 5.972749669260594, 1.585825326448175, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(406914, 'HP:0008251', 'Congenital goiter', 'XPO:0101835', 'abnormal endocrine cell morphology', 0.41304347826086957, 7.428233084304616, 1.7516230275015356, 'UPHENO:0076812', 'abnormal endocrine system morphology'),
(406915, 'HP:0008251', 'Congenital goiter', 'XPO:0129484', 'increased size of the multicellular anatomical structure', 0.41025641025641024, 5.972749669260594, 1.565362206861726, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(406916, 'HP:0008251', 'Congenital goiter', 'XPO:0129487', 'increased size of the anatomical structure', 0.45714285714285713, 5.972749669260594, 1.6523921595084028, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(406917, 'HP:0008251', 'Congenital goiter', 'XPO:0130865', 'increased size of the antero-dorsal region', 0.42105263157894735, 5.972749669260594, 1.585825326448175, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(406918, 'HP:0008251', 'Congenital goiter', 'XPO:0129503', 'increased size of the cell condensation', 0.41025641025641024, 5.972749669260594, 1.565362206861726, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(406919, 'HP:0008251', 'Congenital goiter', 'XPO:0130167', 'increased size of the basal region', 0.41025641025641024, 5.972749669260594, 1.565362206861726, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(406920, 'HP:0008251', 'Congenital goiter', 'XPO:0130552', 'increased size of the ventral region', 0.42105263157894735, 5.972749669260594, 1.585825326448175, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(406921, 'HP:0008251', 'Congenital goiter', 'XPO:0129988', 'increased size of the dorso-lateral region', 0.42105263157894735, 5.972749669260594, 1.585825326448175, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(406922, 'HP:0008251', 'Congenital goiter', 'XPO:0129582', 'increased size of the portion of organism substance', 0.45714285714285713, 5.972749669260594, 1.6523921595084028, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(406923, 'HP:0008251', 'Congenital goiter', 'XPO:0140064', 'abnormally necrotic thyroid', 0.4807692307692308, 11.627087342903641, 2.3643066294231896, 'HP:0011772', 'Abnormal thyroid morphology'),
(406924, 'HP:0008251', 'Congenital goiter', 'XPO:0139937', 'abnormally necrotic ultimobranchial body', 0.42, 7.767034997756375, 1.8061435986813665, 'UPHENO:0087376', 'abnormal endocrine gland morphology'),
(406925, 'HP:0008251', 'Congenital goiter', 'XPO:0129733', 'increased size of the ultimobranchial body', 0.4897959183673469, 7.767034997756375, 1.9504517527274055, 'UPHENO:0087376', 'abnormal endocrine gland morphology'),
(406926, 'HP:0008251', 'Congenital goiter', 'XPO:0130532', 'increased size of the thyroid', 0.5882352941176471, 14.30515924801628, 2.9008273919102177, 'HP:0000853', 'Goiter'),
(406927, 'HP:0008251', 'Congenital goiter', 'XPO:0101857', 'abnormal endocrine system morphology', 0.4634146341463415, 7.428233084304616, 1.8553576251269654, 'UPHENO:0076812', 'abnormal endocrine system morphology'),
(406928, 'HP:0008251', 'Congenital goiter', 'XPO:0130595', 'increased size of the postero-dorsal region', 0.42105263157894735, 5.972749669260594, 1.585825326448175, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(406929, 'HP:0008251', 'Congenital goiter', 'XPO:0102492', 'abnormal parathyroid morphology', 0.4375, 7.767034997756375, 1.8433875912347935, 'UPHENO:0087376', 'abnormal endocrine gland morphology'),
(406930, 'HP:0008251', 'Congenital goiter', 'XPO:0128255', 'decreased size of the endocrine system', 0.425531914893617, 7.428233084304616, 1.7779061416847242, 'UPHENO:0076812', 'abnormal endocrine system morphology'),
(406931, 'HP:0008251', 'Congenital goiter', 'XPO:0125918', 'absent thyroid', 0.40350877192982454, 11.627087342903641, 2.1660174825831517, 'HP:0011772', 'Abnormal thyroid morphology'),
(406932, 'HP:0008251', 'Congenital goiter', 'XPO:0130170', 'increased size of the apical region', 0.41025641025641024, 5.972749669260594, 1.565362206861726, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(406933, 'HP:0008251', 'Congenital goiter', 'XPO:0129571', 'increased size of the anatomical region', 0.43243243243243246, 5.972749669260594, 1.607112524930462, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(406934, 'HP:0008251', 'Congenital goiter', 'XPO:0140281', 'abnormally necrotic endocrine system', 0.41304347826086957, 7.428233084304616, 1.7516230275015356, 'UPHENO:0076812', 'abnormal endocrine system morphology'),
(406935, 'HP:0008251', 'Congenital goiter', 'XPO:0129803', 'increased size of the process', 0.41025641025641024, 5.972749669260594, 1.565362206861726, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(406936, 'HP:0008251', 'Congenital goiter', 'XPO:0102472', 'abnormal thyroid morphology', 0.5434782608695652, 11.627087342903641, 2.5137758866095847, 'HP:0011772', 'Abnormal thyroid morphology'),
(406937, 'HP:0008251', 'Congenital goiter', 'XPO:0141659', 'neoplastic thyroid', 0.5208333333333334, 11.627087342903641, 2.4608483613913137, 'HP:0011772', 'Abnormal thyroid morphology'),
(406938, 'HP:0008251', 'Congenital goiter', 'XPO:0129647', 'increased size of the acellular anatomical structure', 0.41025641025641024, 5.972749669260594, 1.565362206861726, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(406939, 'HP:0008251', 'Congenital goiter', 'XPO:0101561', 'abnormal adrenal cortex', 0.4117647058823529, 7.767034997756375, 1.7883486464974037, 'UPHENO:0087376', 'abnormal endocrine gland morphology'),
(406940, 'HP:0008251', 'Congenital goiter', 'XPO:0129551', 'increased size of the cell part', 0.42857142857142855, 5.972749669260594, 1.5999218287949384, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(406941, 'HP:0008251', 'Congenital goiter', 'XPO:0129517', 'increased size of the anatomical space', 0.43243243243243246, 5.972749669260594, 1.607112524930462, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(406942, 'HP:0041163', 'Fractured manual digit', 'XPO:0101155', 'abnormal forelimb digit 5', 0.42105263157894735, 7.059765001318215, 1.7241034284908738, 'UPHENO:0002708', 'abnormal manus'),
(406943, 'HP:0041163', 'Fractured manual digit', 'XPO:0101810', 'abnormal digit morphology', 0.4927536231884058, 6.466375519622663, 1.7850294020522122, 'UPHENO:0086700', 'abnormal digit morphology'),
(406944, 'HP:0041163', 'Fractured manual digit', 'XPO:0141568', 'abnormal digit-joint region morphology in the regenerating forelimb', 0.4533333333333333, 6.466375519622663, 1.7121400552804105, 'UPHENO:0086700', 'abnormal digit morphology'),
(406945, 'HP:0041163', 'Fractured manual digit', 'XPO:0103634', 'abnormally increased number of forelimb digit', 0.4339622641509434, 7.492661022682715, 1.80320052737318, 'HP:0001167', 'Abnormal finger morphology'),
(406946, 'HP:0041163', 'Fractured manual digit', 'XPO:0103280', 'absent forelimb digit 3', 0.4339622641509434, 7.492661022682715, 1.80320052737318, 'HP:0001167', 'Abnormal finger morphology'),
(406947, 'HP:0041163', 'Fractured manual digit', 'XPO:0130664', 'increased size of the forelimb digit 2', 0.4791666666666667, 7.492661022682715, 1.8947911248214497, 'HP:0001167', 'Abnormal finger morphology'),
(406948, 'HP:0041163', 'Fractured manual digit', 'XPO:0141208', 'abnormally necrotic digit-joint region', 0.4657534246575342, 6.466375519622663, 1.7354355486119033, 'UPHENO:0086700', 'abnormal digit morphology'),
(406949, 'HP:0041163', 'Fractured manual digit', 'XPO:0128213', 'decreased size of the digit', 0.4358974358974359, 6.466375519622663, 1.6788914522843543, 'UPHENO:0086700', 'abnormal digit morphology'),
(406950, 'HP:0041163', 'Fractured manual digit', 'XPO:0102787', 'abnormal forelimb digit 5 morphology', 0.5411764705882353, 7.492661022682715, 2.0136662701573638, 'HP:0001167', 'Abnormal finger morphology'),
(406951, 'HP:0041163', 'Fractured manual digit', 'XPO:0101114', 'abnormal forelimb digit 2', 0.42105263157894735, 7.059765001318215, 1.7241034284908738, 'UPHENO:0002708', 'abnormal manus'),
(406952, 'HP:0041163', 'Fractured manual digit', 'XPO:0140898', 'abnormally necrotic forelimb digit 5', 0.48936170212765956, 7.492661022682715, 1.914842382945809, 'HP:0001167', 'Abnormal finger morphology'),
(406953, 'HP:0041163', 'Fractured manual digit', 'XPO:0100582', 'abnormal forelimb digit', 0.4266666666666667, 7.059765001318215, 1.7355593912518346, 'UPHENO:0002708', 'abnormal manus'),
(406954, 'HP:0041163', 'Fractured manual digit', 'XPO:0141569', 'abnormal digit-joint region morphology in the regenerating hindlimb', 0.4533333333333333, 6.466375519622663, 1.7121400552804105, 'UPHENO:0086700', 'abnormal digit morphology'),
(406955, 'HP:0041163', 'Fractured manual digit', 'XPO:0103279', 'absent forelimb digit 2', 0.4339622641509434, 7.492661022682715, 1.80320052737318, 'HP:0001167', 'Abnormal finger morphology'),
(406956, 'HP:0041163', 'Fractured manual digit', 'XPO:0103779', 'decreased size of the forelimb digit in the regenerating forelimb', 0.45544554455445546, 7.492661022682715, 1.8472950710803275, 'HP:0001167', 'Abnormal finger morphology'),
(406957, 'HP:0041163', 'Fractured manual digit', 'XPO:0103620', 'abnormal number of forelimb digit 3', 0.4125, 7.059765001318215, 1.706503168190368, 'UPHENO:0002708', 'abnormal manus'),
(406958, 'HP:0041163', 'Fractured manual digit', 'XPO:0128497', 'decreased size of the digit-joint region', 0.4533333333333333, 6.466375519622663, 1.7121400552804105, 'UPHENO:0086700', 'abnormal digit morphology'),
(406959, 'HP:0041163', 'Fractured manual digit', 'XPO:0139962', 'abnormally necrotic digit', 0.4473684210526316, 6.466375519622663, 1.7008386772845274, 'UPHENO:0086700', 'abnormal digit morphology'),
(406960, 'HP:0041163', 'Fractured manual digit', 'XPO:0133358', 'fused forelimb digits', 0.5, 7.492661022682715, 1.935543983313569, 'HP:0001167', 'Abnormal finger morphology'),
(406961, 'HP:0041163', 'Fractured manual digit', 'XPO:0103281', 'absent forelimb digit 4', 0.4339622641509434, 7.492661022682715, 1.80320052737318, 'HP:0001167', 'Abnormal finger morphology'),
(406962, 'HP:0041163', 'Fractured manual digit', 'XPO:0102214', 'abnormal forelimb digit morphology', 0.5542168674698795, 7.492661022682715, 2.0377828934910798, 'HP:0001167', 'Abnormal finger morphology'),
(406963, 'HP:0041163', 'Fractured manual digit', 'XPO:0102880', 'abnormal digit-joint region morphology', 0.4927536231884058, 6.466375519622663, 1.7850294020522122, 'UPHENO:0086700', 'abnormal digit morphology'),
(406964, 'HP:0041163', 'Fractured manual digit', 'XPO:0103465', 'bifurcated forelimb digit 2', 0.45098039215686275, 7.492661022682715, 1.8382173990874668, 'HP:0001167', 'Abnormal finger morphology'),
(406965, 'HP:0041163', 'Fractured manual digit', 'XPO:0103611', 'abnormal number of forelimb digits', 0.4230769230769231, 7.059765001318215, 1.7282429384793851, 'UPHENO:0002708', 'abnormal manus'),
(406966, 'HP:0041163', 'Fractured manual digit', 'XPO:0103282', 'absent forelimb digit 5', 0.4339622641509434, 7.492661022682715, 1.80320052737318, 'HP:0001167', 'Abnormal finger morphology'),
(406967, 'HP:0041163', 'Fractured manual digit', 'XPO:0141556', 'abnormal forelimb digit morphology in the regenerating forelimb', 0.5168539325842697, 7.492661022682715, 1.9678951483995373, 'HP:0001167', 'Abnormal finger morphology'),
(406968, 'HP:0041163', 'Fractured manual digit', 'XPO:0129148', 'decreased size of the forelimb digit 4', 0.4742268041237113, 7.492661022682715, 1.8849988570736913, 'HP:0001167', 'Abnormal finger morphology'),
(406969, 'HP:0041163', 'Fractured manual digit', 'XPO:0129161', 'decreased size of the forelimb digit 5', 0.4742268041237113, 7.492661022682715, 1.8849988570736913, 'HP:0001167', 'Abnormal finger morphology'),
(406970, 'HP:0041163', 'Fractured manual digit', 'XPO:0125257', 'absent forelimb digit', 0.44660194174757284, 7.492661022682715, 1.829272249170816, 'HP:0001167', 'Abnormal finger morphology'),
(406971, 'HP:0041163', 'Fractured manual digit', 'XPO:0103467', 'bifurcated forelimb digit 4', 0.45098039215686275, 7.492661022682715, 1.8382173990874668, 'HP:0001167', 'Abnormal finger morphology'),
(406972, 'HP:0041163', 'Fractured manual digit', 'XPO:0100178', 'abnormal digit', 0.4444444444444444, 6.393467666143939, 1.6856871551248356, 'UPHENO:0002905', 'abnormal digit'),
(406973, 'HP:0041163', 'Fractured manual digit', 'XPO:0129188', 'decreased size of the forelimb digit 2', 0.4742268041237113, 7.492661022682715, 1.8849988570736913, 'HP:0001167', 'Abnormal finger morphology'),
(406974, 'HP:0041163', 'Fractured manual digit', 'XPO:0141143', 'abnormally necrotic forelimb digit 3', 0.48936170212765956, 7.492661022682715, 1.914842382945809, 'HP:0001167', 'Abnormal finger morphology'),
(406975, 'HP:0041163', 'Fractured manual digit', 'XPO:0103619', 'abnormal number of forelimb digit 2', 0.4125, 7.059765001318215, 1.706503168190368, 'UPHENO:0002708', 'abnormal manus'),
(406976, 'HP:0041163', 'Fractured manual digit', 'XPO:0100966', 'abnormal forelimb digit 3', 0.42105263157894735, 7.059765001318215, 1.7241034284908738, 'UPHENO:0002708', 'abnormal manus'),
(406977, 'HP:0041163', 'Fractured manual digit', 'XPO:0103466', 'bifurcated forelimb digit 3', 0.45098039215686275, 7.492661022682715, 1.8382173990874668, 'HP:0001167', 'Abnormal finger morphology'),
(406978, 'HP:0041163', 'Fractured manual digit', 'XPO:0103755', 'increased size of the forelimb digit', 0.4946236559139785, 7.492661022682715, 1.9251097079292634, 'HP:0001167', 'Abnormal finger morphology'),
(406979, 'HP:0041163', 'Fractured manual digit', 'XPO:0102598', 'abnormal forelimb digit 3 morphology', 0.5411764705882353, 7.492661022682715, 2.0136662701573638, 'HP:0001167', 'Abnormal finger morphology'),
(406980, 'HP:0041163', 'Fractured manual digit', 'XPO:0130637', 'increased size of the forelimb digit 5', 0.4791666666666667, 7.492661022682715, 1.8947911248214497, 'HP:0001167', 'Abnormal finger morphology'),
(406981, 'HP:0041163', 'Fractured manual digit', 'XPO:0129652', 'increased size of the forelimb digit 3', 0.4791666666666667, 7.492661022682715, 1.8947911248214497, 'HP:0001167', 'Abnormal finger morphology'),
(406982, 'HP:0041163', 'Fractured manual digit', 'XPO:0140219', 'abnormally necrotic forelimb digit', 0.5054945054945055, 7.492661022682715, 1.9461497831613463, 'HP:0001167', 'Abnormal finger morphology'),
(406983, 'HP:0041163', 'Fractured manual digit', 'XPO:0128172', 'decreased size of the forelimb digit 3', 0.4742268041237113, 7.492661022682715, 1.8849988570736913, 'HP:0001167', 'Abnormal finger morphology'),
(406984, 'HP:0041163', 'Fractured manual digit', 'XPO:0129977', 'increased size of the digit-joint region', 0.4533333333333333, 6.466375519622663, 1.7121400552804105, 'UPHENO:0086700', 'abnormal digit morphology'),
(406985, 'HP:0041163', 'Fractured manual digit', 'XPO:0129693', 'increased size of the digit', 0.4358974358974359, 6.466375519622663, 1.6788914522843543, 'UPHENO:0086700', 'abnormal digit morphology'),
(406986, 'HP:0041163', 'Fractured manual digit', 'XPO:0102529', 'abnormal forelimb digit 4 morphology', 0.5411764705882353, 7.492661022682715, 2.0136662701573638, 'HP:0001167', 'Abnormal finger morphology'),
(406987, 'HP:0041163', 'Fractured manual digit', 'XPO:0130624', 'increased size of the forelimb digit 4', 0.4791666666666667, 7.492661022682715, 1.8947911248214497, 'HP:0001167', 'Abnormal finger morphology'),
(406988, 'HP:0041163', 'Fractured manual digit', 'XPO:0103621', 'abnormal number of forelimb digit 4', 0.4125, 7.059765001318215, 1.706503168190368, 'UPHENO:0002708', 'abnormal manus'),
(406989, 'HP:0041163', 'Fractured manual digit', 'XPO:0103622', 'abnormal number of forelimb digit 5', 0.4125, 7.059765001318215, 1.706503168190368, 'UPHENO:0002708', 'abnormal manus'),
(406990, 'HP:0041163', 'Fractured manual digit', 'XPO:0102746', 'abnormal forelimb digit 2 morphology', 0.5411764705882353, 7.492661022682715, 2.0136662701573638, 'HP:0001167', 'Abnormal finger morphology'),
(406991, 'HP:0041163', 'Fractured manual digit', 'XPO:0133378', 'fused forelimb digits part of regenerating forelimb', 0.46464646464646464, 7.492661022682715, 1.8658613171894334, 'HP:0001167', 'Abnormal finger morphology'),
(406992, 'HP:0041163', 'Fractured manual digit', 'XPO:0101248', 'abnormal digit-joint region', 0.42424242424242425, 6.393467666143939, 1.6469305455909364, 'HP:0011297', 'Abnormal digit morphology'),
(406993, 'HP:0041163', 'Fractured manual digit', 'XPO:0103432', 'decreased size of the forelimb digit', 0.48936170212765956, 7.492661022682715, 1.914842382945809, 'HP:0001167', 'Abnormal finger morphology'),
(406994, 'HP:0041163', 'Fractured manual digit', 'XPO:0100897', 'abnormal forelimb digit 4', 0.42105263157894735, 7.059765001318215, 1.7241034284908738, 'UPHENO:0002708', 'abnormal manus'),
(406995, 'HP:0041163', 'Fractured manual digit', 'XPO:0103468', 'bifurcated forelimb digit 5', 0.45098039215686275, 7.492661022682715, 1.8382173990874668, 'HP:0001167', 'Abnormal finger morphology'),
(406996, 'HP:0041163', 'Fractured manual digit', 'XPO:0141108', 'abnormally necrotic forelimb digit 2', 0.48936170212765956, 7.492661022682715, 1.914842382945809, 'HP:0001167', 'Abnormal finger morphology'),
(406997, 'HP:0041163', 'Fractured manual digit', 'XPO:0103609', 'abnormally increased number of forelimb digit in the regenerating forelimb', 0.4107142857142857, 7.492661022682715, 1.7542357082303395, 'HP:0001167', 'Abnormal finger morphology'),
(406998, 'HP:0041163', 'Fractured manual digit', 'XPO:0140716', 'abnormally necrotic forelimb digit 4', 0.48936170212765956, 7.492661022682715, 1.914842382945809, 'HP:0001167', 'Abnormal finger morphology'),
(406999, 'HP:0030427', 'Ossifying fibroma of the jaw', 'XPO:0100647', 'abnormal mouth', 0.42592592592592593, 7.0866363731414825, 1.7373491758799184, 'HP:0000153', 'Abnormality of the mouth'),
(407000, 'HP:0030427', 'Ossifying fibroma of the jaw', 'XPO:0100027', 'abnormal lower jaw', 0.40350877192982454, 7.0866363731414825, 1.6910115138695967, 'HP:0000153', 'Abnormality of the mouth'),
(407001, 'HP:0030427', 'Ossifying fibroma of the jaw', 'XPO:0129152', 'decreased size of the oral cavity', 0.49230769230769234, 7.884497199543557, 1.970177307075115, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(407002, 'HP:0030427', 'Ossifying fibroma of the jaw', 'XPO:0101567', 'abnormal tongue', 0.6274509803921569, 7.884497199543557, 2.22421570396237, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(407003, 'HP:0030427', 'Ossifying fibroma of the jaw', 'XPO:0130628', 'increased size of the oral cavity', 0.49230769230769234, 7.884497199543557, 1.970177307075115, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(407004, 'HP:0030427', 'Ossifying fibroma of the jaw', 'XPO:0141311', 'abnormal roof of mouth morphology', 0.47619047619047616, 7.312692920701687, 1.8660746834314161, 'UPHENO:0076800', 'abnormal mouth morphology'),
(407005, 'HP:0030427', 'Ossifying fibroma of the jaw', 'XPO:0140789', 'abnormally necrotic roof of mouth', 0.4411764705882353, 7.312692920701687, 1.7961592505261732, 'UPHENO:0076800', 'abnormal mouth morphology'),
(407006, 'HP:0030427', 'Ossifying fibroma of the jaw', 'XPO:0103735', 'increased size of the mouth', 0.463768115942029, 7.884497199543557, 1.9122181913637677, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(407007, 'HP:0030427', 'Ossifying fibroma of the jaw', 'XPO:0140626', 'abnormally necrotic tongue', 0.49230769230769234, 7.884497199543557, 1.970177307075115, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(407008, 'HP:0030427', 'Ossifying fibroma of the jaw', 'XPO:0103096', 'abnormal oral cavity morphology', 0.5333333333333333, 7.884497199543557, 2.0506255565290066, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(407009, 'HP:0030427', 'Ossifying fibroma of the jaw', 'XPO:0141830', 'increased width of mouth', 0.43243243243243246, 7.884497199543557, 1.8464864750399128, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(407010, 'HP:0030427', 'Ossifying fibroma of the jaw', 'XPO:0131573', 'decreased size of the roof of mouth', 0.42857142857142855, 7.312692920701687, 1.7703138850862843, 'UPHENO:0076800', 'abnormal mouth morphology'),
(407011, 'HP:0030427', 'Ossifying fibroma of the jaw', 'XPO:0129585', 'increased size of the tongue', 0.41025641025641024, 7.884497199543557, 1.7985175889497047, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(407012, 'HP:0030427', 'Ossifying fibroma of the jaw', 'XPO:0126089', 'absent tongue', 0.5, 7.884497199543557, 1.9855096574360394, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(407013, 'HP:0030427', 'Ossifying fibroma of the jaw', 'XPO:0128105', 'decreased size of the tongue', 0.4383561643835616, 7.884497199543557, 1.859090624602482, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(407014, 'HP:0030427', 'Ossifying fibroma of the jaw', 'XPO:0102960', 'abnormal oral epithelium morphology', 0.43478260869565216, 7.312692920701687, 1.7830961007901136, 'UPHENO:0076800', 'abnormal mouth morphology'),
(407015, 'HP:0030427', 'Ossifying fibroma of the jaw', 'XPO:0115393', 'abnormally decreased volume of oral cavity', 0.47761194029850745, 7.884497199543557, 1.9405488929043109, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(407016, 'HP:0030427', 'Ossifying fibroma of the jaw', 'XPO:0103352', 'decreased size of the mouth', 0.463768115942029, 7.884497199543557, 1.9122181913637677, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(407017, 'HP:0030427', 'Ossifying fibroma of the jaw', 'XPO:0131611', 'increased size of the roof of mouth', 0.42857142857142855, 7.312692920701687, 1.7703138850862843, 'UPHENO:0076800', 'abnormal mouth morphology'),
(407018, 'HP:0030427', 'Ossifying fibroma of the jaw', 'XPO:0101464', 'abnormal oral cavity', 0.41818181818181815, 7.0866363731414825, 1.721482641014341, 'HP:0000153', 'Abnormality of the mouth'),
(407019, 'HP:0030427', 'Ossifying fibroma of the jaw', 'XPO:0101506', 'abnormal upper jaw', 0.40350877192982454, 7.0866363731414825, 1.6910115138695967, 'HP:0000153', 'Abnormality of the mouth'),
(407020, 'HP:0030427', 'Ossifying fibroma of the jaw', 'XPO:0127750', 'abnormally localised tongue', 0.5161290322580645, 7.884497199543557, 2.017279829235854, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(407021, 'HP:0030427', 'Ossifying fibroma of the jaw', 'XPO:0102279', 'abnormal mouth morphology', 0.5, 7.312692920701687, 1.9121575406725366, 'UPHENO:0076800', 'abnormal mouth morphology'),
(407022, 'HP:0030427', 'Ossifying fibroma of the jaw', 'XPO:0103199', 'abnormal tongue morphology', 0.5333333333333333, 7.884497199543557, 2.0506255565290066, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(407023, 'HP:0030427', 'Ossifying fibroma of the jaw', 'XPO:0101816', 'abnormal tooth morphology', 0.4050632911392405, 7.884497199543557, 1.78709831420245, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(407024, 'HP:0030427', 'Ossifying fibroma of the jaw', 'XPO:0115558', 'abnormally incomplete structure of mouth', 0.4918032786885246, 7.312692920701687, 1.8964193508935339, 'UPHENO:0076800', 'abnormal mouth morphology'),
(407025, 'HP:0030427', 'Ossifying fibroma of the jaw', 'XPO:0103828', 'decreased width of the mouth', 0.43243243243243246, 7.884497199543557, 1.8464864750399128, 'UPHENO:0076786', 'abnormal oral cavity morphology'),
(407026, 'HP:0030427', 'Ossifying fibroma of the jaw', 'XPO:0131651', 'abnormal roof of mouth', 0.4107142857142857, 7.0866363731414825, 1.7060430229369012, 'HP:0000153', 'Abnormality of the mouth'),
(407027, 'HP:0003449', 'Cold-induced muscle cramps', 'XPO:0100585', 'abnormal elastica externa', 0.41379310344827586, 3.9037819259951223, 1.270967363209146, 'HP:0033127', 'Abnormality of the musculoskeletal system'),
(407028, 'HP:0003449', 'Cold-induced muscle cramps', 'XPO:0100100', 'abnormal muscle', 0.45161290322580644, 5.968280811662945, 1.6417529121710048, 'UPHENO:0002816', 'abnormal musculature'),
(407029, 'HP:0003449', 'Cold-induced muscle cramps', 'XPO:0100275', 'abnormal skeletal muscle', 0.4375, 5.968280811662945, 1.6158969197020392, 'UPHENO:0002816', 'abnormal musculature'),
(407030, 'HP:0003449', 'Cold-induced muscle cramps', 'XPO:0100004', 'abnormal cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(407031, 'HP:0003449', 'Cold-induced muscle cramps', 'XPO:0100377', 'abnormal connective tissue', 0.41379310344827586, 3.9037819259951223, 1.270967363209146, 'HP:0033127', 'Abnormality of the musculoskeletal system'),
(407032, 'HP:0003449', 'Cold-induced muscle cramps', 'XPO:0100746', 'abnormal smooth muscle', 0.4375, 5.968280811662945, 1.6158969197020392, 'UPHENO:0002816', 'abnormal musculature'),
(407033, 'HP:0034954', 'Thymic carcinoid tumor', 'XPO:0100446', 'abnormal spleen', 0.4067796610169492, 8.696350005340756, 1.8808238373801138, 'UPHENO:0075774', 'abnormal lymphatic part of lymphoid system'),
(407034, 'HP:0034954', 'Thymic carcinoid tumor', 'XPO:0102834', 'abnormal thymus morphology', 0.6071428571428571, 11.145960653167025, 2.6013824010640367, 'UPHENO:0087358', 'abnormal thymus morphology'),
(407035, 'HP:0034954', 'Thymic carcinoid tumor', 'XPO:0100922', 'abnormal lymph vessel', 0.40816326530612246, 8.696350005340756, 1.8840198020256578, 'UPHENO:0075774', 'abnormal lymphatic part of lymphoid system'),
(407036, 'HP:0034954', 'Thymic carcinoid tumor', 'XPO:0140117', 'abnormally necrotic thymocyte', 0.43037974683544306, 11.145960653167025, 2.1902044936826868, 'UPHENO:0087358', 'abnormal thymus morphology'),
(407037, 'HP:0034954', 'Thymic carcinoid tumor', 'XPO:0128866', 'decreased size of the thymus', 0.5151515151515151, 11.145960653167025, 2.3962175440260354, 'UPHENO:0087358', 'abnormal thymus morphology'),
(407038, 'HP:0034954', 'Thymic carcinoid tumor', 'XPO:0130344', 'increased size of the thymus', 0.5151515151515151, 11.145960653167025, 2.3962175440260354, 'UPHENO:0087358', 'abnormal thymus morphology'),
(407039, 'HP:0034954', 'Thymic carcinoid tumor', 'XPO:0141658', 'neoplastic thymus', 0.5862068965517241, 11.145960653167025, 2.5561375165629627, 'UPHENO:0087358', 'abnormal thymus morphology'),
(407040, 'HP:0034954', 'Thymic carcinoid tumor', 'XPO:0140641', 'abnormally necrotic thymus', 0.5483870967741935, 11.145960653167025, 2.4723068182063606, 'UPHENO:0087358', 'abnormal thymus morphology'),
(407041, 'HP:0034954', 'Thymic carcinoid tumor', 'XPO:0102080', 'abnormal thymocyte morphology', 0.4594594594594595, 11.145960653167025, 2.262988523360321, 'UPHENO:0087358', 'abnormal thymus morphology'),
(407042, 'HP:0033358', 'Abnormal urine osmolality', 'XPO:0100069', 'abnormal urinary system', 0.5, 6.355235291121788, 1.7825873458433654, 'HP:0000079', 'Abnormality of the urinary system'),
(407043, 'HP:0033358', 'Abnormal urine osmolality', 'XPO:0124921', 'absent urinary system', 0.41025641025641024, 6.355235291121788, 1.61470617044417, 'HP:0000079', 'Abnormality of the urinary system'),
(407044, 'HP:0033358', 'Abnormal urine osmolality', 'XPO:0100085', 'abnormal mesonephric sinus', 0.42857142857142855, 6.355235291121788, 1.6503551943819923, 'HP:0000079', 'Abnormality of the urinary system'),
(407045, 'HP:0033358', 'Abnormal urine osmolality', 'XPO:0101579', 'abnormal urethra', 0.40540540540540543, 6.355235291121788, 1.6051313776896794, 'HP:0000079', 'Abnormality of the urinary system'),
(407046, 'HP:0033358', 'Abnormal urine osmolality', 'XPO:0100501', 'abnormal urogenital system', 0.4482758620689655, 5.4478002382576385, 1.562727534851952, 'HP:0000119', 'Abnormality of the genitourinary system'),
(407047, 'HP:0033358', 'Abnormal urine osmolality', 'XPO:0101701', 'abnormal urinary system morphology', 0.42105263157894735, 6.355235291121788, 1.6358143365401303, 'HP:0000079', 'Abnormality of the urinary system'),
(407048, 'HP:0033358', 'Abnormal urine osmolality', 'XPO:0101212', 'abnormal glomeral mesenchyme', 0.40625, 5.4478002382576385, 1.4876722914648124, 'HP:0000119', 'Abnormality of the genitourinary system'),
(407049, 'HP:0033358', 'Abnormal urine osmolality', 'XPO:0100761', 'abnormal ureter', 0.40540540540540543, 6.355235291121788, 1.6051313776896794, 'HP:0000079', 'Abnormality of the urinary system'),
(407050, 'HP:0033358', 'Abnormal urine osmolality', 'XPO:0126535', 'abnormally localised urinary system', 0.42105263157894735, 6.355235291121788, 1.6358143365401303, 'HP:0000079', 'Abnormality of the urinary system'),
(407051, 'HP:0033358', 'Abnormal urine osmolality', 'XPO:0100120', 'abnormal genital system', 0.40625, 5.4478002382576385, 1.4876722914648124, 'HP:0000119', 'Abnormality of the genitourinary system'),
(407052, 'HP:0009245', 'Triangular shaped distal phalanx of the 5th finger', 'XPO:0103609', 'abnormally increased number of forelimb digit in the regenerating forelimb', 0.41007194244604317, 7.774297771301195, 1.7855031190763642, 'HP:0005918', 'Abnormal finger phalanx morphology'),
(407053, 'HP:0009245', 'Triangular shaped distal phalanx of the 5th finger', 'XPO:0103634', 'abnormally increased number of forelimb digit', 0.42857142857142855, 7.774297771301195, 1.8253333673568306, 'HP:0005918', 'Abnormal finger phalanx morphology'),
(407054, 'HP:0006735', 'Renal cortical adenoma', 'XPO:0127342', 'abnormally localised mesonephric mesenchyme', 0.40425531914893614, 6.880013295263146, 1.6677175931270638, 'HP:0000077', 'Abnormality of the kidney'),
(407055, 'HP:0006735', 'Renal cortical adenoma', 'XPO:0100085', 'abnormal mesonephric sinus', 0.5757575757575758, 6.880013295263146, 1.9902813308827976, 'HP:0000077', 'Abnormality of the kidney'),
(407056, 'HP:0006735', 'Renal cortical adenoma', 'XPO:0100775', 'abnormal rectal diverticulum', 0.44680851063829785, 6.880013295263146, 1.7532964648422167, 'HP:0000077', 'Abnormality of the kidney'),
(407057, 'HP:0006735', 'Renal cortical adenoma', 'XPO:0126072', 'absent mesonephric sinus', 0.4318181818181818, 6.880013295263146, 1.7236341932224046, 'HP:0000077', 'Abnormality of the kidney'),
(407058, 'HP:0006735', 'Renal cortical adenoma', 'XPO:0100501', 'abnormal urogenital system', 0.41935483870967744, 5.4478002382576385, 1.5114765596055648, 'HP:0000119', 'Abnormality of the genitourinary system'),
(407059, 'HP:0006735', 'Renal cortical adenoma', 'XPO:0100271', 'abnormal mesonephric nephron', 0.4318181818181818, 6.880013295263146, 1.7236341932224046, 'HP:0000077', 'Abnormality of the kidney'),
(407060, 'HP:0006735', 'Renal cortical adenoma', 'XPO:0100270', 'abnormal mesonephric tubule', 0.40425531914893614, 6.880013295263146, 1.6677175931270638, 'HP:0000077', 'Abnormality of the kidney'),
(407061, 'HP:0006735', 'Renal cortical adenoma', 'XPO:0101717', 'abnormal mesonephric sinus morphology', 0.4418604651162791, 6.880013295263146, 1.7435612620872136, 'HP:0000077', 'Abnormality of the kidney'),
(407062, 'HP:0006735', 'Renal cortical adenoma', 'XPO:0100566', 'abnormal kidney', 0.5135135135135135, 6.880013295263146, 1.8796222493549772, 'HP:0000077', 'Abnormality of the kidney'),
(407063, 'HP:0006735', 'Renal cortical adenoma', 'XPO:0100778', 'abnormal mesonephric kidney', 0.4418604651162791, 6.880013295263146, 1.7435612620872136, 'HP:0000077', 'Abnormality of the kidney'),
(407064, 'HP:0006735', 'Renal cortical adenoma', 'XPO:0127733', 'abnormally localised mesonephric sinus', 0.475, 6.880013295263146, 1.8077627928602786, 'HP:0000077', 'Abnormality of the kidney'),
(407065, 'HP:0006735', 'Renal cortical adenoma', 'XPO:0101277', 'abnormal glomerulus', 0.4222222222222222, 6.880013295263146, 1.7043751061443133, 'HP:0000077', 'Abnormality of the kidney'),
(407066, 'HP:0006735', 'Renal cortical adenoma', 'XPO:0100565', 'abnormal pronephric kidney', 0.40425531914893614, 6.880013295263146, 1.6677175931270638, 'HP:0000077', 'Abnormality of the kidney'),
(407067, 'HP:0006735', 'Renal cortical adenoma', 'XPO:0100147', 'abnormal mesonephric mesenchyme', 0.5277777777777778, 6.880013295263146, 1.9055492982485522, 'HP:0000077', 'Abnormality of the kidney'),
(407068, 'HP:0006735', 'Renal cortical adenoma', 'XPO:0107300', 'abnormal embryonic kidney', 0.5, 6.880013295263146, 1.8547254911796445, 'HP:0000077', 'Abnormality of the kidney'),
(407069, 'HP:0006735', 'Renal cortical adenoma', 'XPO:0141613', 'metaplastic kidney', 0.4634146341463415, 6.880013295263146, 1.7855808142300187, 'HP:0000077', 'Abnormality of the kidney'),
(407070, 'HP:0006735', 'Renal cortical adenoma', 'XPO:0100761', 'abnormal ureter', 0.4594594594594595, 6.828345551150745, 1.7712560390677927, 'HP:0010935', 'Abnormality of the upper urinary tract'),
(407071, 'HP:0006735', 'Renal cortical adenoma', 'XPO:0107301', 'abnormal adult kidney', 0.5, 6.880013295263146, 1.8547254911796445, 'HP:0000077', 'Abnormality of the kidney'),
(407072, 'HP:0006735', 'Renal cortical adenoma', 'XPO:0100069', 'abnormal urinary system', 0.46875, 6.355235291121788, 1.725982775902859, 'HP:0000079', 'Abnormality of the urinary system'),
(407073, 'HP:0009529', 'Irregular epiphysis of the proximal phalanx of the 2nd finger', 'XPO:0103634', 'abnormally increased number of forelimb digit', 0.4318181818181818, 7.774297771301195, 1.8322344633033256, 'HP:0005918', 'Abnormal finger phalanx morphology'),
(407074, 'HP:0009529', 'Irregular epiphysis of the proximal phalanx of the 2nd finger', 'XPO:0103609', 'abnormally increased number of forelimb digit in the regenerating forelimb', 0.41304347826086957, 7.774297771301195, 1.7919606559559202, 'HP:0005918', 'Abnormal finger phalanx morphology'),
(407075, 'HP:0008028', 'Cystoid macular degeneration', 'XPO:0128295', 'decreased size of the retinal neural layer', 0.4574468085106383, 8.040873045973026, 1.9178820903589395, 'HP:0000479', 'Abnormal retinal morphology'),
(407076, 'HP:0008028', 'Cystoid macular degeneration', 'XPO:0140487', 'abnormally necrotic retinal layer', 0.5657894736842105, 8.040873045973026, 2.1329419421640696, 'HP:0000479', 'Abnormal retinal morphology'),
(407077, 'HP:0008028', 'Cystoid macular degeneration', 'XPO:0102117', 'abnormal retina morphology', 0.5972222222222222, 8.040873045973026, 2.191389529299339, 'HP:0000479', 'Abnormal retinal morphology'),
(407078, 'HP:0008028', 'Cystoid macular degeneration', 'XPO:0103706', 'increased pigmentation in the optic nerve', 0.4019607843137255, 7.796308075334707, 1.7702570741880883, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(407079, 'HP:0008028', 'Cystoid macular degeneration', 'XPO:0103210', 'abnormal pupil morphology', 0.42168674698795183, 6.887869297006056, 1.7042661756699493, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(407080, 'HP:0008028', 'Cystoid macular degeneration', 'XPO:0129810', 'increased size of the retinal progenitor cell region', 0.5308641975308642, 8.040873045973026, 2.066061861851679, 'HP:0000479', 'Abnormal retinal morphology'),
(407081, 'HP:0008028', 'Cystoid macular degeneration', 'XPO:0102818', 'abnormal optic chiasm morphology', 0.4823529411764706, 7.796308075334707, 1.9392194642318246, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(407082, 'HP:0008028', 'Cystoid macular degeneration', 'XPO:0139731', 'abnormally necrotic eye', 0.4375, 6.887869297006056, 1.7359270772241988, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(407083, 'HP:0008028', 'Cystoid macular degeneration', 'XPO:0102232', 'abnormal eye photoreceptor cell morphology', 0.48314606741573035, 8.040873045973026, 1.9710190741722953, 'HP:0000479', 'Abnormal retinal morphology'),
(407084, 'HP:0008028', 'Cystoid macular degeneration', 'XPO:0129580', 'increased size of the inner limiting membrane', 0.4574468085106383, 8.040873045973026, 1.9178820903589395, 'HP:0000479', 'Abnormal retinal morphology'),
(407085, 'HP:0008028', 'Cystoid macular degeneration', 'XPO:0141343', 'decreased pigmentation in the eye', 0.4605263157894737, 6.887869297006056, 1.7810236020304815, 'HP:0012372', 'Abnormal eye morphology'),
(407086, 'HP:0008028', 'Cystoid macular degeneration', 'XPO:0102226', 'abnormal Jacobsons organ morphology', 0.4117647058823529, 5.788671267106304, 1.5438816411077807, 'UPHENO:0087472', 'abnormal face morphology'),
(407087, 'HP:0008028', 'Cystoid macular degeneration', 'XPO:0130265', 'increased size of the peripheral retina', 0.5180722891566265, 8.040873045973026, 2.0410177622316423, 'HP:0000479', 'Abnormal retinal morphology'),
(407088, 'HP:0008028', 'Cystoid macular degeneration', 'XPO:0129388', 'decreased size of the sclera', 0.43209876543209874, 6.887869297006056, 1.7251781994025936, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(407089, 'HP:0008028', 'Cystoid macular degeneration', 'XPO:0103160', 'abnormal choroid morphology', 0.4189189189189189, 6.575878401988876, 1.6597469298370302, 'UPHENO:0087924', 'abnormal camera-type eye morphology'),
(407090, 'HP:0008028', 'Cystoid macular degeneration', 'XPO:0102663', 'abnormal retinal progenitor cell morphology', 0.5058823529411764, 8.040873045973026, 2.0168628550791743, 'HP:0000479', 'Abnormal retinal morphology'),
(407091, 'HP:0008028', 'Cystoid macular degeneration', 'XPO:0128710', 'decreased size of the optic chiasm', 0.43617021276595747, 7.796308075334707, 1.844049172882245, 'UPHENO:0021656', 'abnormal ocular fundus morphology'),
(407092, 'HP:0008028', 'Cystoid macular degeneration', 'XPO:0128669', 'decreased size of the ciliary marginal zone', 0.4777777777777778, 8.040873045973026, 1.960038381077836, 'HP:0000479', 'Abnormal retinal morphology'),
(407093, 'HP:0008028', 'Cystoid macular degeneration', 'XPO:0140945', 'abnormally necrotic retinal ganglion cell layer', 0.46236559139784944, 8.040873045973026, 1.9281657141584967, 'HP:0000479', 'Abnormal retinal morphology'),
(407094, 'HP:0008028', 'Cystoid macular degeneration', 'XPO:0103086', 'abnormal amacrine cell morphology', 0.46236559139784944, 8.040873045973026, 1.9281657141584967, 'HP:0000479', 'Abnormal retinal morphology'),
(407095, 'HP:0008028', 'Cystoid macular degeneration', 'XPO:0100329', 'abnormal retinal blood vessel', 0.6056338028169014, 8.040873045973026, 2.206767890105474, 'HP:0000479', 'Abnormal retinal morphology'),
(407096, 'HP:0008028', 'Cystoid macular degeneration', 'XPO:0140218', 'abnormally necrotic sclera', 0.4430379746835443, 6.887869297006056, 1.7468794071802813, 'HP:0012372', 'Abnormal eye morphology'),
(407097, 'HP:0008028', 'Cystoid macular degeneration', 'XPO:0101315', 'abnormal hyaloid vascular plexus', 0.43661971830985913, 6.887869297006056, 1.734179792355427, 'HP:0012372', 'Abnormal eye morphology'),
