(312486, 'HP:0034639', 'Bloodstream microfilaria', 'XPO:0100638', 'abnormal polar body', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(312487, 'HP:0034639', 'Bloodstream microfilaria', 'XPO:0141272', 'absent surface breathing', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312488, 'HP:0034639', 'Bloodstream microfilaria', 'XPO:0141748', 'abnormal gas homeostasis', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312489, 'HP:0034639', 'Bloodstream microfilaria', 'XPO:0141864', 'abnormal 5-methylcytosine metabolic process', 0.4230769230769231, 4.758907843651163, 1.418937661667548, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(312490, 'HP:0034639', 'Bloodstream microfilaria', 'XPO:0107312', 'abnormal filopodium', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(312491, 'HP:0034639', 'Bloodstream microfilaria', 'XPO:0100724', 'abnormal kinetochore', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(312492, 'HP:0034639', 'Bloodstream microfilaria', 'XPO:0101132', 'abnormal apoptotic cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(312493, 'HP:0034639', 'Bloodstream microfilaria', 'XPO:0100372', 'abnormal hematological system', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(312494, 'HP:0034639', 'Bloodstream microfilaria', 'XPO:0141771', 'abnormal urea homeostasis', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312495, 'HP:0034639', 'Bloodstream microfilaria', 'XPO:0133388', 'absent insulin receptor signaling pathway', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312496, 'HP:0034639', 'Bloodstream microfilaria', 'XPO:0141904', 'abnormal glucosamine metabolic process', 0.5238095238095238, 4.758907843651163, 1.5788480773767701, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(312497, 'HP:0034639', 'Bloodstream microfilaria', 'XPO:0107262', 'abnormal left-right axis', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312498, 'HP:0034639', 'Bloodstream microfilaria', 'XPO:0101366', 'abnormal morula cell', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(312499, 'HP:0034639', 'Bloodstream microfilaria', 'XPO:0100585', 'abnormal elastica externa', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(312500, 'HP:0034639', 'Bloodstream microfilaria', 'XPO:0131729', 'abnormal regulation of growth rate', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312501, 'HP:0034639', 'Bloodstream microfilaria', 'XPO:0101480', 'abnormal stage V oocyte', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(312502, 'HP:0034639', 'Bloodstream microfilaria', 'XPO:0141908', 'abnormal pyridine metabolic process', 0.4230769230769231, 4.758907843651163, 1.418937661667548, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(312503, 'HP:0034639', 'Bloodstream microfilaria', 'XPO:0101157', 'abnormal female organism', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312504, 'HP:0034639', 'Bloodstream microfilaria', 'XPO:0142057', 'abnormal desmosome', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(312505, 'HP:0034639', 'Bloodstream microfilaria', 'XPO:0101110', 'abnormal cell-free extract', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312506, 'HP:0034639', 'Bloodstream microfilaria', 'XPO:0141852', 'abnormal glucose metabolic process', 0.4230769230769231, 4.758907843651163, 1.418937661667548, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(312507, 'HP:0034639', 'Bloodstream microfilaria', 'XPO:0131675', 'abnormal spindle microtubule', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(312508, 'HP:0034639', 'Bloodstream microfilaria', 'XPO:0141880', 'abnormal ethanolamine metabolic process', 0.44, 4.758907843651163, 1.447038165082909, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(312509, 'HP:0034639', 'Bloodstream microfilaria', 'XPO:0100581', 'abnormal immune system', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(312510, 'HP:0034639', 'Bloodstream microfilaria', 'XPO:0141266', 'abnormal surface breathing', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312511, 'HP:0034639', 'Bloodstream microfilaria', 'XPO:0131691', 'abnormal molecular function', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312512, 'HP:0034639', 'Bloodstream microfilaria', 'XPO:0101547', 'abnormal lampbrush chromosome', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(312513, 'HP:0034639', 'Bloodstream microfilaria', 'XPO:0141772', 'abnormal water homeostasis', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312514, 'HP:0034639', 'Bloodstream microfilaria', 'XPO:0100721', 'abnormal centromere', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(312515, 'HP:0034639', 'Bloodstream microfilaria', 'XPO:0100899', 'abnormal secondary spermatogonium', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(312516, 'HP:0034639', 'Bloodstream microfilaria', 'XPO:0100802', 'abnormal exocrine cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(312517, 'HP:0034639', 'Bloodstream microfilaria', 'XPO:0101373', 'abnormal oxygen accumulating cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(312518, 'HP:0034639', 'Bloodstream microfilaria', 'XPO:0100317', 'abnormal respiratory system', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(312519, 'HP:0034639', 'Bloodstream microfilaria', 'XPO:0141781', 'abnormal secondary metabolic process', 0.5238095238095238, 4.758907843651163, 1.5788480773767701, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(312520, 'HP:0034639', 'Bloodstream microfilaria', 'XPO:0141770', 'abnormal urate homeostasis', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312521, 'HP:0032766', 'Focal autonomic seizure with hypoventilation/hyperventilation/altered respiration', 'XPO:0100642', 'abnormal gustatory system', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(312522, 'HP:0032766', 'Focal autonomic seizure with hypoventilation/hyperventilation/altered respiration', 'XPO:0100587', 'abnormal vestibuloauditory system', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(312523, 'HP:0032766', 'Focal autonomic seizure with hypoventilation/hyperventilation/altered respiration', 'XPO:0100273', 'abnormal visual system', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(312524, 'HP:0032766', 'Focal autonomic seizure with hypoventilation/hyperventilation/altered respiration', 'XPO:0100032', 'abnormal nervous system', 0.43333333333333335, 3.94131651835137, 1.3068679445984308, 'UPHENO:0004523', 'abnormal nervous system'),
(312525, 'HP:0032766', 'Focal autonomic seizure with hypoventilation/hyperventilation/altered respiration', 'XPO:0100274', 'abnormal sensory system', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(312526, 'HP:0032766', 'Focal autonomic seizure with hypoventilation/hyperventilation/altered respiration', 'XPO:0107253', 'abnormal enteric nervous system', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(312527, 'HP:0032766', 'Focal autonomic seizure with hypoventilation/hyperventilation/altered respiration', 'XPO:0100427', 'abnormal olfactory system', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(312528, 'HP:0032766', 'Focal autonomic seizure with hypoventilation/hyperventilation/altered respiration', 'XPO:0100031', 'abnormal central nervous system', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(312529, 'HP:0008443', 'Neuropathic spinal arthropathy', 'XPO:0139998', 'abnormally necrotic axial skeleton', 0.42857142857142855, 6.211345574613551, 1.6315652749010534, 'UPHENO:0087089', 'abnormal axial skeleton plus cranial skeleton morphology'),
(312530, 'HP:0008443', 'Neuropathic spinal arthropathy', 'XPO:0102806', 'abnormal articular system morphology', 0.5128205128205128, 4.638757693672553, 1.5423521320759594, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(312531, 'HP:0008443', 'Neuropathic spinal arthropathy', 'XPO:0140269', 'abnormally necrotic anatomical line', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(312532, 'HP:0008443', 'Neuropathic spinal arthropathy', 'XPO:0102761', 'abnormal cartilaginous condensation morphology', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(312533, 'HP:0008443', 'Neuropathic spinal arthropathy', 'XPO:0129638', 'increased size of the skeletal subdivision', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(312534, 'HP:0008443', 'Neuropathic spinal arthropathy', 'XPO:0141316', 'abnormal anatomical region morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(312535, 'HP:0008443', 'Neuropathic spinal arthropathy', 'XPO:0102564', 'abnormal olfactory region morphology', 0.41818181818181815, 6.272837960958401, 1.6196255072310737, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(312536, 'HP:0008443', 'Neuropathic spinal arthropathy', 'XPO:0128727', 'decreased size of the vertebral element', 0.4126984126984127, 8.361863005979023, 1.8576672440911264, 'UPHENO:0076695', 'abnormal vertebral column morphology'),
(312537, 'HP:0008443', 'Neuropathic spinal arthropathy', 'XPO:0140043', 'abnormally necrotic perichondrium', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(312538, 'HP:0008443', 'Neuropathic spinal arthropathy', 'XPO:0101755', 'abnormal pelvic girdle morphology', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(312539, 'HP:0008443', 'Neuropathic spinal arthropathy', 'XPO:0102401', 'abnormal neurocranium morphology', 0.41818181818181815, 6.272837960958401, 1.6196255072310737, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(312540, 'HP:0008443', 'Neuropathic spinal arthropathy', 'XPO:0102773', 'abnormal Keller explant morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(312541, 'HP:0008443', 'Neuropathic spinal arthropathy', 'XPO:0100927', 'abnormal sacral vertebra', 0.43103448275862066, 8.05344015541032, 1.863145300778979, 'UPHENO:0002813', 'abnormal vertebral column'),
(312542, 'HP:0008443', 'Neuropathic spinal arthropathy', 'XPO:0129434', 'decreased size of the notochordal sheath', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(312543, 'HP:0008443', 'Neuropathic spinal arthropathy', 'XPO:0103116', 'abnormal bone marrow morphology', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(312544, 'HP:0008443', 'Neuropathic spinal arthropathy', 'XPO:0100422', 'abnormal notochord', 0.4117647058823529, 4.3395673355180735, 1.3367425584480601, 'UPHENO:0002964', 'abnormal skeletal system'),
(312545, 'HP:0008443', 'Neuropathic spinal arthropathy', 'XPO:0130368', 'increased size of the elastica externa', 0.4444444444444444, 4.638757693672553, 1.4358516936218344, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(312546, 'HP:0008443', 'Neuropathic spinal arthropathy', 'XPO:0139771', 'abnormally necrotic skeletal subdivision', 0.43478260869565216, 4.638757693672553, 1.4201588541997616, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(312547, 'HP:0008443', 'Neuropathic spinal arthropathy', 'XPO:0128352', 'decreased size of the skeletal system', 0.4444444444444444, 4.638757693672553, 1.4358516936218344, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(312548, 'HP:0008443', 'Neuropathic spinal arthropathy', 'XPO:0125894', 'absent vertebral element', 0.4098360655737705, 8.05344015541032, 1.816752660002781, 'UPHENO:0002813', 'abnormal vertebral column'),
(312549, 'HP:0008443', 'Neuropathic spinal arthropathy', 'XPO:0100585', 'abnormal elastica externa', 0.42424242424242425, 4.3395673355180735, 1.3568450783281876, 'UPHENO:0002964', 'abnormal skeletal system'),
(312550, 'HP:0008443', 'Neuropathic spinal arthropathy', 'XPO:0101860', 'abnormal skeletal subdivision morphology', 0.4878048780487805, 4.638757693672553, 1.5042634845863214, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(312551, 'HP:0008443', 'Neuropathic spinal arthropathy', 'XPO:0129832', 'increased size of the skeletal system', 0.4444444444444444, 4.638757693672553, 1.4358516936218344, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(312552, 'HP:0008443', 'Neuropathic spinal arthropathy', 'XPO:0139889', 'abnormally necrotic cranial skeleton', 0.42, 6.211345574613551, 1.61516721776344, 'UPHENO:0087089', 'abnormal axial skeleton plus cranial skeleton morphology'),
(312553, 'HP:0008443', 'Neuropathic spinal arthropathy', 'XPO:0128709', 'decreased size of the flexural organ', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(312554, 'HP:0008443', 'Neuropathic spinal arthropathy', 'XPO:0129664', 'increased size of the skeleton', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(312555, 'HP:0008443', 'Neuropathic spinal arthropathy', 'XPO:0102742', 'abnormal cell-free extract morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(312556, 'HP:0008443', 'Neuropathic spinal arthropathy', 'XPO:0141723', 'abnormal posterior notochord morphology', 0.5, 4.638757693672553, 1.5229507040072823, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(312557, 'HP:0008443', 'Neuropathic spinal arthropathy', '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'),
(312558, 'HP:0008443', 'Neuropathic spinal arthropathy', 'XPO:0139917', 'abnormally necrotic notochord', 0.43478260869565216, 4.638757693672553, 1.4201588541997616, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(312559, 'HP:0008443', 'Neuropathic spinal arthropathy', 'XPO:0102054', 'abnormal notochord morphology', 0.5, 4.638757693672553, 1.5229507040072823, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(312560, 'HP:0008443', 'Neuropathic spinal arthropathy', 'XPO:0102144', 'abnormal cranial skeleton morphology', 0.4772727272727273, 6.211345574613551, 1.7217740393063181, 'UPHENO:0087089', 'abnormal axial skeleton plus cranial skeleton morphology'),
(312561, 'HP:0008443', 'Neuropathic spinal arthropathy', 'XPO:0102010', 'abnormal perichondrium morphology', 0.4878048780487805, 4.638757693672553, 1.5042634845863214, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(312562, 'HP:0008443', 'Neuropathic spinal arthropathy', 'XPO:0102605', 'abnormal dermal skeleton morphology', 0.46511627906976744, 4.638757693672553, 1.4688640910537754, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(312563, 'HP:0008443', 'Neuropathic spinal arthropathy', 'XPO:0125164', 'absent vertebral centrum', 0.4032258064516129, 8.05344015541032, 1.8020418700394085, 'UPHENO:0002813', 'abnormal vertebral column'),
(312564, 'HP:0008443', 'Neuropathic spinal arthropathy', 'XPO:0102728', 'abnormal tendon morphology', 0.43478260869565216, 4.638757693672553, 1.4201588541997616, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(312565, 'HP:0008443', 'Neuropathic spinal arthropathy', 'XPO:0130908', 'increased size of the notochordal sheath', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(312566, 'HP:0008443', 'Neuropathic spinal arthropathy', 'XPO:0140852', 'abnormally necrotic vertebral centrum', 0.41935483870967744, 8.361863005979023, 1.8725885058348382, 'UPHENO:0076695', 'abnormal vertebral column morphology'),
(312567, 'HP:0008443', 'Neuropathic spinal arthropathy', 'XPO:0126886', 'abnormally localised vertebral column', 0.5102040816326531, 8.05344015541032, 2.0270416962841815, 'UPHENO:0002813', 'abnormal vertebral column'),
(312568, 'HP:0008443', 'Neuropathic spinal arthropathy', 'XPO:0140103', 'abnormally necrotic vertebral column', 0.5098039215686274, 8.361863005979023, 2.0646817072051897, 'UPHENO:0076695', 'abnormal vertebral column morphology'),
(312569, 'HP:0008443', 'Neuropathic spinal arthropathy', 'XPO:0128890', 'decreased size of the elastica externa', 0.4444444444444444, 4.638757693672553, 1.4358516936218344, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(312570, 'HP:0008443', 'Neuropathic spinal arthropathy', 'XPO:0102514', 'abnormal perichondrial cell morphology', 0.4444444444444444, 4.638757693672553, 1.4358516936218344, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(312571, 'HP:0008443', 'Neuropathic spinal arthropathy', 'XPO:0128306', 'decreased size of the articular system', 0.43478260869565216, 4.638757693672553, 1.4201588541997616, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(312572, 'HP:0008443', 'Neuropathic spinal arthropathy', 'XPO:0101446', 'abnormal transverse process', 0.423728813559322, 8.05344015541032, 1.8472884566637167, 'UPHENO:0002813', 'abnormal vertebral column'),
(312573, 'HP:0008443', 'Neuropathic spinal arthropathy', 'XPO:0107345', 'abnormal anatomical axis morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(312574, 'HP:0008443', 'Neuropathic spinal arthropathy', 'XPO:0103737', 'increased size of the notochord', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(312575, 'HP:0008443', 'Neuropathic spinal arthropathy', 'XPO:0140144', 'abnormally necrotic portion of organism substance', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(312576, 'HP:0008443', 'Neuropathic spinal arthropathy', 'XPO:0101981', 'abnormal ossicle morphology', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(312577, 'HP:0008443', 'Neuropathic spinal arthropathy', 'XPO:0101226', 'abnormal postsacral vertebra', 0.43103448275862066, 8.05344015541032, 1.863145300778979, 'UPHENO:0002813', 'abnormal vertebral column'),
(312578, 'HP:0008443', 'Neuropathic spinal arthropathy', 'XPO:0100465', 'abnormal skeletal system', 0.4117647058823529, 4.3395673355180735, 1.3367425584480601, 'UPHENO:0002964', 'abnormal skeletal system'),
(312579, 'HP:0008443', 'Neuropathic spinal arthropathy', 'XPO:0140350', 'abnormally necrotic notochordal sheath', 0.4444444444444444, 4.638757693672553, 1.4358516936218344, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(312580, 'HP:0008443', 'Neuropathic spinal arthropathy', 'XPO:0129707', 'increased size of the vertebral column', 0.49056603773584906, 8.361863005979023, 2.025350834530429, 'UPHENO:0076695', 'abnormal vertebral column morphology'),
(312581, 'HP:0008443', 'Neuropathic spinal arthropathy', 'XPO:0102325', 'abnormal vertebral centrum morphology', 0.48148148148148145, 8.361863005979023, 2.006509952146755, 'UPHENO:0076695', 'abnormal vertebral column morphology'),
(312582, 'HP:0008443', 'Neuropathic spinal arthropathy', 'XPO:0101680', 'abnormal skeletal element morphology', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(312583, 'HP:0008443', 'Neuropathic spinal arthropathy', 'XPO:0130188', 'increased size of the flexural organ', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(312584, 'HP:0008443', 'Neuropathic spinal arthropathy', 'XPO:0130427', 'increased size of the vertebral centrum', 0.40625, 8.361863005979023, 1.843097079965941, 'UPHENO:0076695', 'abnormal vertebral column morphology'),
(312585, 'HP:0008443', 'Neuropathic spinal arthropathy', 'XPO:0102113', 'abnormal anatomical line morphology', 0.43333333333333335, 2.786899518863159, 1.0989342374200721, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(312586, 'HP:0008443', 'Neuropathic spinal arthropathy', 'XPO:0100253', 'abnormal vertebra', 0.43859649122807015, 8.05344015541032, 1.8794176210938882, 'UPHENO:0002813', 'abnormal vertebral column'),
(312587, 'HP:0008443', 'Neuropathic spinal arthropathy', 'XPO:0128132', 'decreased size of the perichondrium', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(312588, 'HP:0008443', 'Neuropathic spinal arthropathy', 'XPO:0102980', 'abnormal perichordal tissue morphology', 0.45454545454545453, 4.638757693672553, 1.452076521536181, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(312589, 'HP:0008443', 'Neuropathic spinal arthropathy', 'XPO:0128184', 'decreased size of the skeleton', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(312590, 'HP:0008443', 'Neuropathic spinal arthropathy', 'XPO:0140108', 'abnormally necrotic dermal skeleton', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(312591, 'HP:0008443', 'Neuropathic spinal arthropathy', 'XPO:0140019', 'abnormally necrotic skeletal system', 0.46511627906976744, 4.638757693672553, 1.4688640910537754, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(312592, 'HP:0008443', 'Neuropathic spinal arthropathy', 'XPO:0103152', 'abnormal otic region morphology', 0.41818181818181815, 6.272837960958401, 1.6196255072310737, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(312593, 'HP:0008443', 'Neuropathic spinal arthropathy', 'XPO:0102130', 'abnormal endoskeleton morphology', 0.46511627906976744, 4.638757693672553, 1.4688640910537754, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(312594, 'HP:0008443', 'Neuropathic spinal arthropathy', 'XPO:0103355', 'decreased size of the notochord', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(312595, 'HP:0008443', 'Neuropathic spinal arthropathy', 'XPO:0102216', 'abnormal vertebral column morphology', 0.5777777777777777, 8.361863005979023, 2.1980215252987785, 'UPHENO:0076695', 'abnormal vertebral column morphology'),
(312596, 'HP:0008443', 'Neuropathic spinal arthropathy', 'XPO:0100226', 'abnormal vertebral element', 0.5434782608695652, 8.05344015541032, 2.0920969503537643, 'UPHENO:0002813', 'abnormal vertebral column'),
(312597, 'HP:0008443', 'Neuropathic spinal arthropathy', 'XPO:0100693', 'abnormal vertebral centrum', 0.5319148936170213, 8.05344015541032, 2.0697209385605895, 'UPHENO:0002813', 'abnormal vertebral column'),
(312598, 'HP:0008443', 'Neuropathic spinal arthropathy', 'XPO:0102702', 'abnormal rib morphology', 0.40625, 8.361863005979023, 1.843097079965941, 'UPHENO:0076695', 'abnormal vertebral column morphology'),
(312599, 'HP:0008443', 'Neuropathic spinal arthropathy', 'XPO:0141699', 'abnormally necrotic anterior notochord', 0.4444444444444444, 4.638757693672553, 1.4358516936218344, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(312600, 'HP:0008443', 'Neuropathic spinal arthropathy', 'XPO:0102542', 'abnormal vacuolated notochordal tissue morphology', 0.45454545454545453, 4.638757693672553, 1.452076521536181, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(312601, 'HP:0008443', 'Neuropathic spinal arthropathy', 'XPO:0141703', 'abnormally necrotic posterior notochord', 0.4444444444444444, 4.638757693672553, 1.4358516936218344, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(312602, 'HP:0008443', 'Neuropathic spinal arthropathy', 'XPO:0102351', 'abnormal sphenoid region morphology', 0.41818181818181815, 6.272837960958401, 1.6196255072310737, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(312603, 'HP:0008443', 'Neuropathic spinal arthropathy', 'XPO:0101890', 'abnormal organ part morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(312604, 'HP:0008443', 'Neuropathic spinal arthropathy', 'XPO:0141709', 'increased size of the anterior notochord', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(312605, 'HP:0008443', 'Neuropathic spinal arthropathy', 'XPO:0141713', 'increased size of the posterior notochord', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(312606, 'HP:0008443', 'Neuropathic spinal arthropathy', 'XPO:0101740', 'abnormal cell part morphology', 0.4166666666666667, 2.786899518863159, 1.0775936770692605, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(312607, 'HP:0008443', 'Neuropathic spinal arthropathy', 'XPO:0100584', 'abnormal vertebral column', 0.625, 8.05344015541032, 2.2435240353362498, 'UPHENO:0002813', 'abnormal vertebral column'),
(312608, 'HP:0008443', 'Neuropathic spinal arthropathy', 'XPO:0140559', 'abnormally necrotic articular system', 0.45454545454545453, 4.638757693672553, 1.452076521536181, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(312609, 'HP:0008443', 'Neuropathic spinal arthropathy', 'XPO:0102828', 'abnormal occipital region morphology', 0.42592592592592593, 6.272837960958401, 1.6345532468244968, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(312610, 'HP:0008443', 'Neuropathic spinal arthropathy', 'XPO:0128949', 'decreased size of the vertebral centrum', 0.40625, 8.361863005979023, 1.843097079965941, 'UPHENO:0076695', 'abnormal vertebral column morphology'),
(312611, 'HP:0008443', 'Neuropathic spinal arthropathy', 'XPO:0125260', 'absent vertebral column', 0.4807692307692308, 8.05344015541032, 1.9677007466997247, 'UPHENO:0002813', 'abnormal vertebral column'),
(312612, 'HP:0008443', 'Neuropathic spinal arthropathy', 'XPO:0101982', 'abnormal appendicular skeleton morphology', 0.4444444444444444, 4.638757693672553, 1.4358516936218344, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(312613, 'HP:0008443', 'Neuropathic spinal arthropathy', 'XPO:0126787', 'abnormally localised vertebral centrum', 0.43103448275862066, 8.05344015541032, 1.863145300778979, 'UPHENO:0002813', 'abnormal vertebral column'),
(312614, 'HP:0008443', 'Neuropathic spinal arthropathy', 'XPO:0129612', 'increased size of the perichondrium', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(312615, 'HP:0008443', 'Neuropathic spinal arthropathy', 'XPO:0101694', 'abnormal anatomical space morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(312616, 'HP:0008443', 'Neuropathic spinal arthropathy', 'XPO:0128158', 'decreased size of the skeletal subdivision', 0.4166666666666667, 4.638757693672553, 1.3902574242552699, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(312617, 'HP:0008443', 'Neuropathic spinal arthropathy', 'XPO:0129786', 'increased size of the articular system', 0.43478260869565216, 4.638757693672553, 1.4201588541997616, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(312618, 'HP:0008443', 'Neuropathic spinal arthropathy', 'XPO:0128397', 'decreased size of the cranial skeleton', 0.40384615384615385, 6.211345574613551, 1.5838017617482976, 'UPHENO:0087089', 'abnormal axial skeleton plus cranial skeleton morphology'),
(312619, 'HP:0008443', 'Neuropathic spinal arthropathy', 'XPO:0101854', 'abnormal bone element morphology', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(312620, 'HP:0008443', 'Neuropathic spinal arthropathy', 'XPO:0130205', 'increased size of the vertebral element', 0.4126984126984127, 8.361863005979023, 1.8576672440911264, 'UPHENO:0076695', 'abnormal vertebral column morphology'),
(312621, 'HP:0008443', 'Neuropathic spinal arthropathy', 'XPO:0100895', 'abnormal presacral vertebra', 0.43103448275862066, 8.05344015541032, 1.863145300778979, 'UPHENO:0002813', 'abnormal vertebral column'),
(312622, 'HP:0008443', 'Neuropathic spinal arthropathy', 'XPO:0102567', 'abnormal skeleton morphology', 0.5, 4.638757693672553, 1.5229507040072823, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(312623, 'HP:0008443', 'Neuropathic spinal arthropathy', 'XPO:0139718', 'abnormally necrotic anatomical structure', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(312624, 'HP:0008443', 'Neuropathic spinal arthropathy', 'XPO:0103218', 'abnormal joint morphology', 0.43478260869565216, 4.638757693672553, 1.4201588541997616, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(312625, 'HP:0008443', 'Neuropathic spinal arthropathy', 'XPO:0101636', 'abnormal cell morphology', 0.40540540540540543, 2.786899518863159, 1.0629318554210558, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(312626, 'HP:0008443', 'Neuropathic spinal arthropathy', 'XPO:0101070', 'abnormal rib', 0.423728813559322, 8.05344015541032, 1.8472884566637167, 'UPHENO:0002813', 'abnormal vertebral column'),
(312627, 'HP:0008443', 'Neuropathic spinal arthropathy', 'XPO:0107372', 'abnormal flexural organ morphology', 0.5, 4.638757693672553, 1.5229507040072823, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(312628, 'HP:0008443', 'Neuropathic spinal arthropathy', 'XPO:0139795', 'abnormally necrotic vertebral element', 0.4262295081967213, 8.361863005979023, 1.8878751962581628, 'UPHENO:0076695', 'abnormal vertebral column morphology'),
(312629, 'HP:0008443', 'Neuropathic spinal arthropathy', 'XPO:0102272', 'abnormal notochordal sheath morphology', 0.5, 4.638757693672553, 1.5229507040072823, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(312630, 'HP:0008443', 'Neuropathic spinal arthropathy', 'XPO:0140123', 'abnormally necrotic perichondrial cell', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(312631, 'HP:0008443', 'Neuropathic spinal arthropathy', 'XPO:0102009', 'abnormal connective tissue morphology', 0.41025641025641024, 3.9037819259951223, 1.2655242231512656, 'HP:0033127', 'Abnormality of the musculoskeletal system'),
(312632, 'HP:0008443', 'Neuropathic spinal arthropathy', 'XPO:0101957', 'abnormal axial skeleton morphology', 0.4883720930232558, 6.211345574613551, 1.7416796027871364, 'UPHENO:0087089', 'abnormal axial skeleton plus cranial skeleton morphology'),
(312633, 'HP:0008443', 'Neuropathic spinal arthropathy', 'XPO:0102178', 'abnormal whole organism morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(312634, 'HP:0008443', 'Neuropathic spinal arthropathy', 'XPO:0141719', 'abnormal anterior notochord morphology', 0.5, 4.638757693672553, 1.5229507040072823, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(312635, 'HP:0008443', 'Neuropathic spinal arthropathy', 'XPO:0102164', 'abnormal mandibular mesenchyme morphology', 0.42857142857142855, 6.211345574613551, 1.6315652749010534, 'UPHENO:0087089', 'abnormal axial skeleton plus cranial skeleton morphology'),
(312636, 'HP:0008443', 'Neuropathic spinal arthropathy', 'XPO:0128246', 'decreased size of the axial skeleton', 0.4117647058823529, 6.211345574613551, 1.599253852164941, 'UPHENO:0087089', 'abnormal axial skeleton plus cranial skeleton morphology'),
(312637, 'HP:0008443', 'Neuropathic spinal arthropathy', 'XPO:0102093', 'abnormal craniofacial skeleton morphology', 0.45652173913043476, 6.211345574613551, 1.6839282300806968, 'UPHENO:0087089', 'abnormal axial skeleton plus cranial skeleton morphology'),
(312638, 'HP:0008443', 'Neuropathic spinal arthropathy', 'XPO:0129877', 'increased size of the cranial skeleton', 0.40384615384615385, 6.211345574613551, 1.5838017617482976, 'UPHENO:0087089', 'abnormal axial skeleton plus cranial skeleton morphology'),
(312639, 'HP:0008443', 'Neuropathic spinal arthropathy', 'XPO:0140510', 'abnormally necrotic postcranial axial skeleton', 0.46, 6.272837960958401, 1.69867756270602, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(312640, 'HP:0008443', 'Neuropathic spinal arthropathy', 'XPO:0140812', 'abnormally necrotic endoskeleton', 0.40816326530612246, 4.638757693672553, 1.3759979968056957, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(312641, 'HP:0008443', 'Neuropathic spinal arthropathy', 'XPO:0101858', 'abnormal vertebral element morphology', 0.49056603773584906, 8.361863005979023, 2.025350834530429, 'UPHENO:0076695', 'abnormal vertebral column morphology'),
(312642, 'HP:0008443', 'Neuropathic spinal arthropathy', 'XPO:0102217', 'abnormal elastica externa morphology', 0.5263157894736842, 4.638757693672553, 1.5625144536043167, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(312643, 'HP:0008443', 'Neuropathic spinal arthropathy', 'XPO:0127548', 'abnormally localised vertebral element', 0.43859649122807015, 8.05344015541032, 1.8794176210938882, 'UPHENO:0002813', 'abnormal vertebral column'),
(312644, 'HP:0008443', 'Neuropathic spinal arthropathy', 'XPO:0128227', 'decreased size of the vertebral column', 0.49056603773584906, 8.361863005979023, 2.025350834530429, 'UPHENO:0076695', 'abnormal vertebral column morphology'),
(312645, 'HP:0008443', 'Neuropathic spinal arthropathy', 'XPO:0140432', 'abnormally necrotic skeleton', 0.4444444444444444, 4.638757693672553, 1.4358516936218344, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(312646, 'HP:0008443', 'Neuropathic spinal arthropathy', 'XPO:0101976', 'abnormal portion of organism substance morphology', 0.43333333333333335, 2.786899518863159, 1.0989342374200721, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(312647, 'HP:0008443', 'Neuropathic spinal arthropathy', 'XPO:0102461', 'abnormal postcranial axial skeleton morphology', 0.5227272727272727, 6.272837960958401, 1.810796366130629, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(312648, 'HP:0008443', 'Neuropathic spinal arthropathy', 'XPO:0100252', 'abnormal caudal vertebra', 0.4166666666666667, 8.05344015541032, 1.8318297040812228, 'UPHENO:0002813', 'abnormal vertebral column'),
(312649, 'HP:0008443', 'Neuropathic spinal arthropathy', 'XPO:0141708', 'decreased size of the posterior notochord', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(312650, 'HP:0008443', 'Neuropathic spinal arthropathy', 'XPO:0139774', 'abnormally necrotic elastica externa', 0.46511627906976744, 4.638757693672553, 1.4688640910537754, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(312651, 'HP:0008443', 'Neuropathic spinal arthropathy', 'XPO:0102097', 'abnormal skeletal system morphology', 0.5263157894736842, 4.638757693672553, 1.5625144536043167, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(312652, 'HP:0008443', 'Neuropathic spinal arthropathy', 'XPO:0128580', 'decreased size of the postcranial axial skeleton', 0.4423076923076923, 6.272837960958401, 1.6656903922192745, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(312653, 'HP:0008443', 'Neuropathic spinal arthropathy', 'XPO:0129726', 'increased size of the axial skeleton', 0.4117647058823529, 6.211345574613551, 1.599253852164941, 'UPHENO:0087089', 'abnormal axial skeleton plus cranial skeleton morphology'),
(312654, 'HP:0008443', 'Neuropathic spinal arthropathy', 'XPO:0103201', 'abnormal activin-induced ectoderm morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(312655, 'HP:0008443', 'Neuropathic spinal arthropathy', 'XPO:0101638', 'abnormal anatomical structure morphology', 0.43333333333333335, 2.786899518863159, 1.0989342374200721, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(312656, 'HP:0008443', 'Neuropathic spinal arthropathy', 'XPO:0140683', 'abnormally necrotic flexural organ', 0.4444444444444444, 4.638757693672553, 1.4358516936218344, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(312657, 'HP:0008443', 'Neuropathic spinal arthropathy', 'XPO:0130060', 'increased size of the postcranial axial skeleton', 0.4423076923076923, 6.272837960958401, 1.6656903922192745, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(312658, 'HP:0008443', 'Neuropathic spinal arthropathy', 'XPO:0101713', 'abnormal anatomical entity in vitro morphology', 0.43333333333333335, 2.786899518863159, 1.0989342374200721, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(312659, 'HP:0008443', 'Neuropathic spinal arthropathy', 'XPO:0141704', 'decreased size of the anterior notochord', 0.425531914893617, 4.638757693672553, 1.404969552736279, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(312660, 'HP:0001700', 'Myocardial necrosis', 'XPO:0139990', 'abnormally necrotic cardiovascular system', 0.40476190476190477, 5.9590888072311134, 1.5530653998657664, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(312661, 'HP:0001700', 'Myocardial necrosis', 'XPO:0102532', 'abnormal angioblast morphology', 0.4146341463414634, 5.9590888072311134, 1.57189112236161, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(312662, 'HP:0001700', 'Myocardial necrosis', 'XPO:0102800', 'abnormal circulating cell morphology', 0.4146341463414634, 5.9590888072311134, 1.57189112236161, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(312663, 'HP:0001700', 'Myocardial necrosis', 'XPO:0139811', 'abnormally necrotic circulatory system', 0.40476190476190477, 5.9590888072311134, 1.5530653998657664, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(312664, 'HP:0001700', 'Myocardial necrosis', 'XPO:0101919', 'abnormal heart primordium morphology', 0.4146341463414634, 5.9590888072311134, 1.57189112236161, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(312665, 'HP:0001700', 'Myocardial necrosis', 'XPO:0102935', 'abnormal bulbous arteriosis morphology', 0.4358974358974359, 5.9590888072311134, 1.6116921329326988, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(312666, 'HP:0001700', 'Myocardial necrosis', 'XPO:0101900', 'abnormal circulatory system morphology', 0.4722222222222222, 5.9590888072311134, 1.6775023573665249, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(312667, 'HP:0001700', 'Myocardial necrosis', 'XPO:0141328', 'edematous circulatory system', 0.4358974358974359, 5.9590888072311134, 1.6116921329326988, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(312668, 'HP:0001700', 'Myocardial necrosis', 'XPO:0101995', 'abnormal cardiovascular system morphology', 0.4722222222222222, 5.9590888072311134, 1.6775023573665249, 'HP:0030680', 'Abnormal cardiovascular system morphology'),
(312669, 'HP:0011209', 'EEG with generalized slow activity grade 4', 'XPO:0107253', 'abnormal enteric nervous system', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(312670, 'HP:0011209', 'EEG with generalized slow activity grade 4', 'XPO:0100587', 'abnormal vestibuloauditory system', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(312671, 'HP:0011209', 'EEG with generalized slow activity grade 4', 'XPO:0100427', 'abnormal olfactory system', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(312672, 'HP:0011209', 'EEG with generalized slow activity grade 4', 'XPO:0100032', 'abnormal nervous system', 0.43333333333333335, 3.94131651835137, 1.3068679445984308, 'UPHENO:0004523', 'abnormal nervous system'),
(312673, 'HP:0011209', 'EEG with generalized slow activity grade 4', 'XPO:0100031', 'abnormal central nervous system', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(312674, 'HP:0011209', 'EEG with generalized slow activity grade 4', 'XPO:0100273', 'abnormal visual system', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(312675, 'HP:0011209', 'EEG with generalized slow activity grade 4', 'XPO:0100274', 'abnormal sensory system', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(312676, 'HP:0011209', 'EEG with generalized slow activity grade 4', 'XPO:0100642', 'abnormal gustatory system', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(312677, 'HP:0008708', 'Partial development of the penile shaft', 'XPO:0102270', 'abnormal polar body morphology', 0.46808510638297873, 7.005035523447265, 1.810787894318205, 'UPHENO:0020950', 'abnormal reproductive system morphology'),
(312678, 'HP:0008708', 'Partial development of the penile shaft', 'XPO:0126964', 'abnormally localised female genitalia', 0.43137254901960786, 7.005035523447265, 1.7383267902561792, 'UPHENO:0020950', 'abnormal reproductive system morphology'),
(312679, 'HP:0008708', 'Partial development of the penile shaft', 'XPO:0100765', 'abnormal male genitalia', 0.6, 8.414388317771037, 2.246916329252743, 'HP:0010461', 'Abnormality of the male genitalia'),
(312680, 'HP:0008708', 'Partial development of the penile shaft', 'XPO:0130505', 'increased size of the male genitalia', 0.4444444444444444, 8.414388317771037, 1.9338376718927501, 'HP:0010461', 'Abnormality of the male genitalia'),
(312681, 'HP:0008708', 'Partial development of the penile shaft', 'XPO:0101372', 'abnormal seminiferous tubule', 0.4528301886792453, 8.414388317771037, 1.9519961704769546, 'HP:0010461', 'Abnormality of the male genitalia'),
(312682, 'HP:0008708', 'Partial development of the penile shaft', 'XPO:0102133', 'abnormal urogenital system morphology', 0.4146341463414634, 5.4478002382576385, 1.5029451091868848, 'HP:0000119', 'Abnormality of the genitourinary system'),
(312683, 'HP:0008708', 'Partial development of the penile shaft', 'XPO:0102864', 'abnormal female genitalia morphology', 0.4583333333333333, 7.005035523447265, 1.7918262420167856, 'HP:0012243', 'Abnormal reproductive system morphology'),
(312684, 'HP:0008708', 'Partial development of the penile shaft', 'XPO:0129028', 'decreased size of the male genitalia', 0.4444444444444444, 8.414388317771037, 1.9338376718927501, 'HP:0010461', 'Abnormality of the male genitalia'),
(312685, 'HP:0008708', 'Partial development of the penile shaft', 'XPO:0102894', 'abnormal oviduct morphology', 0.4230769230769231, 7.005035523447265, 1.7215309684419309, 'UPHENO:0020950', 'abnormal reproductive system morphology'),
(312686, 'HP:0008708', 'Partial development of the penile shaft', 'XPO:0125335', 'absent female genitalia', 0.4230769230769231, 7.005035523447265, 1.7215309684419309, 'UPHENO:0020950', 'abnormal reproductive system morphology'),
(312687, 'HP:0008708', 'Partial development of the penile shaft', 'XPO:0101232', 'abnormal female genitalia', 0.5238095238095238, 7.005035523447265, 1.915542826930714, 'HP:0012243', 'Abnormal reproductive system morphology'),
(312688, 'HP:0008708', 'Partial development of the penile shaft', 'XPO:0101752', 'abnormal genital system morphology', 0.5238095238095238, 7.005035523447265, 1.915542826930714, 'UPHENO:0020950', 'abnormal reproductive system morphology'),
(312689, 'HP:0008708', 'Partial development of the penile shaft', 'XPO:0129864', 'increased size of the genital system', 0.4489795918367347, 7.005035523447265, 1.7734480511475887, 'UPHENO:0020950', 'abnormal reproductive system morphology'),
(312690, 'HP:0008708', 'Partial development of the penile shaft', 'XPO:0101262', 'abnormal oviduct', 0.4782608695652174, 7.005035523447265, 1.8303645486020337, 'HP:0012243', 'Abnormal reproductive system morphology'),
(312691, 'HP:0008708', 'Partial development of the penile shaft', 'XPO:0126762', 'abnormally localised male genitalia', 0.4897959183673469, 8.414388317771037, 2.030106660646711, 'HP:0010461', 'Abnormality of the male genitalia'),
(312692, 'HP:0008708', 'Partial development of the penile shaft', 'XPO:0125139', 'absent male genitalia', 0.48, 8.414388317771037, 2.009703060785373, 'HP:0010461', 'Abnormality of the male genitalia'),
(312693, 'HP:0008708', 'Partial development of the penile shaft', 'XPO:0100414', 'abnormal testis', 0.48, 8.414388317771037, 2.009703060785373, 'HP:0010461', 'Abnormality of the male genitalia'),
(312694, 'HP:0008708', 'Partial development of the penile shaft', 'XPO:0140723', 'abnormally necrotic polar body', 0.43137254901960786, 7.005035523447265, 1.7383267902561792, 'UPHENO:0020950', 'abnormal reproductive system morphology'),
(312695, 'HP:0008708', 'Partial development of the penile shaft', 'XPO:0140839', 'abnormally necrotic female genitalia', 0.4074074074074074, 7.005035523447265, 1.689349981917436, 'HP:0012243', 'Abnormal reproductive system morphology'),
(312696, 'HP:0008708', 'Partial development of the penile shaft', 'XPO:0100666', 'abnormal primary spermatogonium', 0.43636363636363634, 8.414388317771037, 1.916176683951214, 'HP:0010461', 'Abnormality of the male genitalia'),
(312697, 'HP:0008708', 'Partial development of the penile shaft', 'XPO:0128384', 'decreased size of the genital system', 0.4489795918367347, 7.005035523447265, 1.7734480511475887, 'HP:0012243', 'Abnormal reproductive system morphology'),
(312698, 'HP:0008708', 'Partial development of the penile shaft', 'XPO:0102397', 'abnormal male genitalia morphology', 0.5217391304347826, 8.414388317771037, 2.095260280741859, 'HP:0010461', 'Abnormality of the male genitalia'),
(312699, 'HP:0008708', 'Partial development of the penile shaft', 'XPO:0101948', 'abnormal gamete morphology', 0.40816326530612246, 6.723205497167461, 1.656552295898908, 'UPHENO:0087547', 'abnormal reproductive system morphology'),
(312700, 'HP:0008708', 'Partial development of the penile shaft', 'XPO:0101669', 'abnormal gonad morphology', 0.40816326530612246, 6.723205497167461, 1.656552295898908, 'UPHENO:0087547', 'abnormal reproductive system morphology'),
(312701, 'HP:0008708', 'Partial development of the penile shaft', 'XPO:0139867', 'abnormally necrotic genital system', 0.46808510638297873, 7.005035523447265, 1.810787894318205, 'UPHENO:0020950', 'abnormal reproductive system morphology'),
(312702, 'HP:0008708', 'Partial development of the penile shaft', 'XPO:0139866', 'abnormally necrotic male genitalia', 0.46153846153846156, 8.414388317771037, 1.9706759852830318, 'HP:0010461', 'Abnormality of the male genitalia'),
(312703, 'HP:0005328', 'Progeroid facial appearance', 'XPO:0100544', 'abnormal neuromast support cell', 0.42857142857142855, 6.8660902472206855, 1.7154037734456928, 'HP:0000951', 'Abnormality of the skin'),
(312704, 'HP:0005328', 'Progeroid facial appearance', 'XPO:0102139', 'abnormal skin morphology', 0.45, 7.420886955069779, 1.8274022900777487, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(312705, 'HP:0005328', 'Progeroid facial appearance', 'XPO:0102176', 'abnormal neuromast support cell morphology', 0.4186046511627907, 7.420886955069779, 1.7625032752155354, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(312706, 'HP:0005328', 'Progeroid facial appearance', 'XPO:0102840', 'abnormal stratum spongiosum morphology', 0.4186046511627907, 7.420886955069779, 1.7625032752155354, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(312707, 'HP:0005328', 'Progeroid facial appearance', 'XPO:0101254', 'abnormal stratum compactum', 0.42857142857142855, 6.8660902472206855, 1.7154037734456928, 'HP:0000951', 'Abnormality of the skin'),
(312708, 'HP:0005328', 'Progeroid facial appearance', 'XPO:0101387', 'abnormal melanophore', 0.4166666666666667, 6.8660902472206855, 1.6914109306558096, 'HP:0000951', 'Abnormality of the skin'),
(312709, 'HP:0005328', 'Progeroid facial appearance', 'XPO:0100004', 'abnormal cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(312710, 'HP:0005328', 'Progeroid facial appearance', 'XPO:0100983', 'abnormal skin gland', 0.46875, 6.8660902472206855, 1.7940122082596586, 'HP:0000951', 'Abnormality of the skin'),
(312711, 'HP:0005328', 'Progeroid facial appearance', 'XPO:0101515', 'abnormal neuromast mantle cell', 0.42857142857142855, 6.8660902472206855, 1.7154037734456928, 'HP:0000951', 'Abnormality of the skin'),
(312712, 'HP:0005328', 'Progeroid facial appearance', 'XPO:0102727', 'abnormal skin seromucous gland morphology', 0.42857142857142855, 7.420886955069779, 1.7833620281931915, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(312713, 'HP:0005328', 'Progeroid facial appearance', 'XPO:0102910', 'abnormal pigment cell morphology', 0.4186046511627907, 7.420886955069779, 1.7625032752155354, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(312714, 'HP:0005328', 'Progeroid facial appearance', 'XPO:0101322', 'abnormal iridophore', 0.4166666666666667, 6.8660902472206855, 1.6914109306558096, 'HP:0000951', 'Abnormality of the skin'),
(312715, 'HP:0005328', 'Progeroid facial appearance', 'XPO:0101095', 'abnormal skin seromucous gland', 0.45454545454545453, 6.8660902472206855, 1.7666211003984522, 'HP:0000951', 'Abnormality of the skin'),
(312716, 'HP:0005328', 'Progeroid facial appearance', 'XPO:0102626', 'abnormal granular gland morphology', 0.42857142857142855, 7.420886955069779, 1.7833620281931915, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(312717, 'HP:0005328', 'Progeroid facial appearance', 'XPO:0100929', 'abnormal dermis', 0.45454545454545453, 6.8660902472206855, 1.7666211003984522, 'HP:0000951', 'Abnormality of the skin'),
(312718, 'HP:0005328', 'Progeroid facial appearance', 'XPO:0102561', 'abnormal dermis morphology', 0.43902439024390244, 7.420886955069779, 1.8049793268950312, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(312719, 'HP:0005328', 'Progeroid facial appearance', 'XPO:0101278', 'abnormal pigment cell', 0.42857142857142855, 6.8660902472206855, 1.7154037734456928, 'HP:0000951', 'Abnormality of the skin'),
(312720, 'HP:0005328', 'Progeroid facial appearance', 'XPO:0101529', 'abnormal skin mucous gland', 0.42857142857142855, 6.8660902472206855, 1.7154037734456928, 'HP:0000951', 'Abnormality of the skin'),
(312721, 'HP:0005328', 'Progeroid facial appearance', 'XPO:0100507', 'abnormal skin', 0.4838709677419355, 6.8660902472206855, 1.8227182263109507, 'HP:0000951', 'Abnormality of the skin'),
(312722, 'HP:0005328', 'Progeroid facial appearance', 'XPO:0101313', 'abnormal Eberth-Kastschenko layer', 0.42857142857142855, 6.8660902472206855, 1.7154037734456928, 'HP:0000951', 'Abnormality of the skin'),
(312723, 'HP:0005328', 'Progeroid facial appearance', 'XPO:0102886', 'abnormal stratum compactum morphology', 0.4186046511627907, 7.420886955069779, 1.7625032752155354, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(312724, 'HP:0005328', 'Progeroid facial appearance', 'XPO:0101591', 'abnormal xanthophore', 0.4166666666666667, 6.8660902472206855, 1.6914109306558096, 'HP:0000951', 'Abnormality of the skin'),
(312725, 'HP:0005328', 'Progeroid facial appearance', 'XPO:0100994', 'abnormal granular gland', 0.45454545454545453, 6.8660902472206855, 1.7666211003984522, 'HP:0000951', 'Abnormality of the skin'),
(312726, 'HP:0005328', 'Progeroid facial appearance', 'XPO:0103147', 'abnormal neuromast mantle cell morphology', 0.4186046511627907, 7.420886955069779, 1.7625032752155354, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(312727, 'HP:0005328', 'Progeroid facial appearance', 'XPO:0102615', 'abnormal skin gland morphology', 0.45, 7.420886955069779, 1.8274022900777487, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(312728, 'HP:0005328', 'Progeroid facial appearance', 'XPO:0101208', 'abnormal stratum spongiosum', 0.42857142857142855, 6.8660902472206855, 1.7154037734456928, 'HP:0000951', 'Abnormality of the skin'),
(312729, 'HP:0005328', 'Progeroid facial appearance', 'XPO:0102945', 'abnormal Eberth-Kastschenko layer morphology', 0.4186046511627907, 7.420886955069779, 1.7625032752155354, 'UPHENO:0076739', 'abnormal skin of body morphology'),
(312730, 'HP:0031610', 'Recurrent shoulder dislocation', 'XPO:0100584', 'abnormal vertebral column', 0.4107142857142857, 6.272837960958401, 1.6050994245019483, 'UPHENO:0022529', 'abnormal postcranial axial skeleton morphology'),
(312731, 'HP:0009895', 'Abnormality of the crus of the helix', 'XPO:0102720', 'abnormal dermatocranium morphology', 0.40625, 4.638757693672553, 1.3727692133255593, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(312732, 'HP:0009895', 'Abnormality of the crus of the helix', 'XPO:0101764', 'abnormal cranium morphology', 0.41935483870967744, 4.638757693672553, 1.394734915474381, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(312733, 'HP:0009895', 'Abnormality of the crus of the helix', 'XPO:0129785', 'increased size of the tympanic disk', 0.40816326530612246, 10.484129389061598, 2.0686315489548313, 'UPHENO:0005986', 'abnormal shape of external ear'),
(312734, 'HP:0009895', 'Abnormality of the crus of the helix', 'XPO:0102005', 'abnormal splanchnocranium morphology', 0.40625, 4.638757693672553, 1.3727692133255593, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(312735, 'HP:0009895', 'Abnormality of the crus of the helix', 'XPO:0126939', 'abnormally localised auditory apparatus', 0.4583333333333333, 10.484129389061598, 2.192082564591618, 'UPHENO:0005986', 'abnormal shape of external ear'),
(312736, 'HP:0009895', 'Abnormality of the crus of the helix', 'XPO:0102913', 'abnormal tympanic disk morphology', 0.4268292682926829, 10.151353911937244, 2.081560703513649, 'UPHENO:0086699', 'abnormal external ear morphology'),
(312737, 'HP:0009895', 'Abnormality of the crus of the helix', 'XPO:0102665', 'abnormal suspensorium morphology', 0.40625, 4.638757693672553, 1.3727692133255593, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(312738, 'HP:0009895', 'Abnormality of the crus of the helix', 'XPO:0101681', 'abnormal chondrocranium morphology', 0.40625, 4.638757693672553, 1.3727692133255593, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(312739, 'HP:0009895', 'Abnormality of the crus of the helix', 'XPO:0102092', 'abnormal ethmoid region morphology', 0.4126984126984127, 4.638757693672553, 1.3836213127410304, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(312740, 'HP:0009895', 'Abnormality of the crus of the helix', 'XPO:0102776', 'abnormal fenestra subocularis morphology', 0.4126984126984127, 4.638757693672553, 1.3836213127410304, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(312741, 'HP:0009895', 'Abnormality of the crus of the helix', 'XPO:0103176', 'abnormal fenestra basicranialis morphology', 0.4126984126984127, 4.638757693672553, 1.3836213127410304, 'UPHENO:0076703', 'abnormal skeletal system morphology'),
(312742, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0132842', 'abnormal development of cementoblast', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312743, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0133299', 'abnormal development of centromere', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312744, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0131997', 'abnormal development of early embryonic cell', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312745, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0131864', 'abnormal development of coelom', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312746, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0133321', 'abnormal development of endoplasmic reticulum', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312747, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0131677', 'abnormal actin filament', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(312748, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0141272', 'absent surface breathing', 0.6666666666666666, 1.4755025719078136, 0.9918005753536725, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312749, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100423', 'abnormal process', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312750, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100800', 'abnormal ventral marginal zone', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312751, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0133164', 'abnormal development of archenteron roof midline', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312752, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100493', 'abnormal liver and biliary system', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(312753, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0107276', 'abnormal dorsal region', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312754, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0107259', 'abnormal animal-vegetal axis', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312755, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0141810', 'abnormal cyclase activity', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312756, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100642', 'abnormal gustatory system', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(312757, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0131774', 'abnormal development of anatomical cluster', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312758, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0141760', 'abnormal multicellular organismal homeostasis', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312759, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100823', 'abnormal blood', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(312760, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0141816', 'abnormal ligase activity', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312761, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0141772', 'abnormal water homeostasis', 0.6666666666666666, 1.4755025719078136, 0.9918005753536725, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312762, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0133068', 'abnormal development of joint region', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312763, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0133026', 'abnormal development of forebrain-midbrain boundary', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312764, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100484', 'abnormal cement gland primordium', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312765, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100427', 'abnormal olfactory system', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(312766, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0115508', 'abnormally peramorphic growth of whole organism', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312767, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100014', 'abnormal tissue', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312768, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100862', 'abnormal blastomere V1', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(312769, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100164', 'abnormal neural nucleus', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(312770, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100265', 'abnormal sensory epithelial cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(312771, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0142054', 'abnormal digestive tract', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(312772, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0132807', 'abnormal development of anterior endomesoderm', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312773, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0131901', 'abnormal development of pigment cell', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312774, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0141884', 'abnormal phosphagen metabolic process', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(312775, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100827', 'abnormal atypical epithelium', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312776, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0141860', 'abnormal malate-aspartate shuttle', 0.5263157894736842, 1.8210412618256888, 0.9790009036675816, 'HP:0000118', 'Phenotypic abnormality'),
(312777, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0133182', 'abnormal development of melanoblast', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312778, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0141759', 'abnormal lipid homeostasis', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312779, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100750', 'abnormal regenerating fin', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312780, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100547', 'abnormal blastomere V2', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(312781, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0101472', 'abnormal zygote cortex', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(312782, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0131669', 'abnormal Roux spot', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(312783, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100503', 'abnormal blastomere D2', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(312784, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0142051', 'abnormal cerebrospinal fluid', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(312785, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100551', 'abnormal oocyte cortex', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(312786, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0131408', 'abnormal feeding behavior', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312787, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0132536', 'abnormal development of choana', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312788, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0101311', 'abnormal bottle cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(312789, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0133261', 'abnormal development of pronephric sinus', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312790, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0131693', 'abnormal NAD-retinol dehydrogenase activity', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312791, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0141902', 'abnormal D-methionine transport', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312792, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0131702', 'abnormal canonical Wnt signaling pathway', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312793, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100393', 'abnormal involuting marginal zone', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312794, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0107271', 'abnormal apical region', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312795, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0131401', 'abnormal behavioral response to pain', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312796, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0133335', 'abnormal development of postero-ventral region', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312797, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0131403', 'abnormal mechanosensory behavior', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312798, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0141777', 'abnormal catabolic process', 0.5555555555555556, 1.8210412618256888, 1.005827813247954, 'HP:0000118', 'Phenotypic abnormality'),
(312799, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0107265', 'abnormal posterior side', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312800, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100956', 'abnormal centrosome', 0.5263157894736842, 1.8210412618256888, 0.9790009036675816, 'HP:0000118', 'Phenotypic abnormality'),
(312801, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100242', 'abnormal right lymph heart', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(312802, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100999', 'abnormal serous membrane', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312803, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0133400', 'absent determination of left/right symmetry in intestine', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312804, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0141753', 'abnormal homeostasis of number of cells', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312805, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100372', 'abnormal hematological system', 0.5263157894736842, 1.8210412618256888, 0.9790009036675816, 'HP:0000118', 'Phenotypic abnormality'),
(312806, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0131729', 'abnormal regulation of growth rate', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312807, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0132007', 'abnormal development of extracellular matrix', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312808, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0132482', 'abnormal development of presumptive axial mesoderm', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312809, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0103623', 'absent axon regeneration in optic nerve', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312810, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0101176', 'abnormal non-ciliated epithelial cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(312811, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100501', 'abnormal urogenital system', 0.5263157894736842, 1.8210412618256888, 0.9790009036675816, 'HP:0000118', 'Phenotypic abnormality'),
(312812, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0107264', 'abnormal anterior side', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312813, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0141746', 'abnormal energy homeostasis', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312814, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0141814', 'abnormal lyase activity', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312815, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0133403', 'abnormal developmental process', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312816, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100307', 'abnormal blastomere', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(312817, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100196', 'abnormal neuron', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(312818, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0115362', 'abnormally decreased adhesivity of prechordal plate', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312819, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0131909', 'abnormal development of blastopore lip', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312820, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0101237', 'abnormal mucus secreting cell', 0.5555555555555556, 1.8210412618256888, 1.005827813247954, 'HP:0000118', 'Phenotypic abnormality'),
(312821, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0141964', 'absent cilium motility in olfactory pit', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312822, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0131743', 'abnormal establishment of planar polarity', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312823, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100251', 'abnormal proteinaceous extracellular matrix', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312824, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100721', 'abnormal centromere', 0.5263157894736842, 1.8210412618256888, 0.9790009036675816, 'HP:0000118', 'Phenotypic abnormality'),
(312825, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0132117', 'abnormal development of process', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312826, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0107273', 'abnormal basal region', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312827, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0141877', 'abnormal 2-deoxyribose 1-phosphate metabolic process', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(312828, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100858', 'abnormal presumptive midbrain-hindbrain boundary', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(312829, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0133198', 'abnormal development of actin filament', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312830, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0132439', 'abnormal development of lower blastopore lip', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312831, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0131480', 'absent mating behavior', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312832, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0141963', 'absent cilium motility in pronephric nephrostome', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312833, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0107312', 'abnormal filopodium', 0.5263157894736842, 1.8210412618256888, 0.9790009036675816, 'HP:0000118', 'Phenotypic abnormality'),
(312834, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0101241', 'abnormal nucleate erythrocyte', 0.5555555555555556, 1.8210412618256888, 1.005827813247954, 'HP:0000118', 'Phenotypic abnormality'),
(312835, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100667', 'abnormal vegetal yolk mass', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312836, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100218', 'abnormal epithelial cell', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(312837, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0107288', 'abnormal larval alimentary system', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(312838, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0141892', 'abnormal inositol metabolic process', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(312839, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100674', 'abnormal secondary oogonium', 0.5263157894736842, 1.8210412618256888, 0.9790009036675816, 'HP:0000118', 'Phenotypic abnormality'),
(312840, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0101403', 'abnormal basal lamina', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312841, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100521', 'abnormal animal blastomere', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(312842, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100175', 'abnormal migrating neuroblast', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(312843, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0141782', 'abnormal methylation', 0.5555555555555556, 1.8210412618256888, 1.005827813247954, 'HP:0000118', 'Phenotypic abnormality'),
(312844, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0101560', 'abnormal compound organ component', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312845, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0131727', 'abnormal protein kinase B signaling', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312846, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0101096', 'abnormal tendon', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(312847, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0132847', 'abnormal development of perivitelline space', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312848, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0107268', 'abnormal left side', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312849, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0131993', 'abnormal development of stem cell', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312850, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0132688', 'abnormal development of nucleus', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312851, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0107311', 'abnormal apical junction complex', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(312852, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0132219', 'abnormal development of mouth', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312853, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0141790', 'abnormal cellular metabolic process', 0.5263157894736842, 1.8210412618256888, 0.9790009036675816, 'HP:0000118', 'Phenotypic abnormality'),
(312854, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0133148', 'abnormal development of hindlimb region', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312855, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0131478', 'absent optokinetic behavior', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312856, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0101467', 'abnormal alkali secreting cell', 0.5555555555555556, 1.8210412618256888, 1.005827813247954, 'HP:0000118', 'Phenotypic abnormality'),
(312857, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100025', 'abnormal oocyte', 0.5263157894736842, 1.8210412618256888, 0.9790009036675816, 'HP:0000118', 'Phenotypic abnormality'),
(312858, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0131711', 'abnormal establishment of cell polarity', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312859, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0131732', 'abnormal sex differentiation', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312860, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0101187', 'abnormal dorsolateral commissural neuron', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(312861, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0132739', 'abnormal development of egg jelly', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312862, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0141462', 'abnormal development of tadpole', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312863, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100069', 'abnormal urinary system', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(312864, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0133137', 'abnormal development of posterior endoderm', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312865, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0101373', 'abnormal oxygen accumulating cell', 0.5555555555555556, 1.8210412618256888, 1.005827813247954, 'HP:0000118', 'Phenotypic abnormality'),
(312866, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0101083', 'abnormal T cell', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(312867, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100416', 'abnormal ligament', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(312868, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0141866', 'abnormal dicarboxylic acid metabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(312869, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0132435', 'abnormal development of pupil', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312870, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0101518', 'abnormal B cell', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(312871, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100067', 'abnormal animal hemisphere', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312872, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0141968', 'absent cilium motility in ciliated cell', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312873, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0101513', 'abnormal basal body', 0.5263157894736842, 1.8210412618256888, 0.9790009036675816, 'HP:0000118', 'Phenotypic abnormality'),
(312874, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0131699', 'abnormal axon extension involved in axon guidance', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(312875, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0141812', 'abnormal transferase activity', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312876, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0133149', 'abnormal development of dorsal foregut', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312877, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0115574', 'abnormal variability of size of hindlimb', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(312878, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0101157', 'abnormal female organism', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312879, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100239', 'abnormal acellular anatomical structure', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312880, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0131827', 'abnormal development of neuron', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312881, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0131759', 'abnormal development of cell', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312882, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0101535', 'abnormal absorptive cell', 0.5555555555555556, 1.8210412618256888, 1.005827813247954, 'HP:0000118', 'Phenotypic abnormality'),
(312883, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0133340', 'abnormal cell adhesion', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312884, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0141718', 'abnormal posterior notochord', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(312885, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0141757', 'abnormal ion homeostasis', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312886, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0131862', 'abnormal development of pharyngeal region', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312887, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0132785', 'abnormal development of oocyte cortex', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312888, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0131761', 'abnormal development of multi-tissue structure', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312889, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100976', 'abnormal multiciliated cell', 0.5263157894736842, 1.8210412618256888, 0.9790009036675816, 'HP:0000118', 'Phenotypic abnormality'),
(312890, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0115512', 'abnormally semi-erect whole organism', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312891, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0141745', 'abnormal creatinine homeostasis', 0.6666666666666666, 1.4755025719078136, 0.9918005753536725, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312892, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0131667', 'abnormal actin cytoskeleton', 0.5263157894736842, 1.8210412618256888, 0.9790009036675816, 'HP:0000118', 'Phenotypic abnormality'),
(312893, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100062', 'abnormal anatomical space', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312894, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0133140', 'abnormal development of basal lamina', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312895, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100010', 'abnormal multicellular anatomical structure', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312896, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100533', 'abnormal melanoblast', 0.5555555555555556, 1.8210412618256888, 1.005827813247954, 'HP:0000118', 'Phenotypic abnormality'),
(312897, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0126318', 'abnormally localised cell', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(312898, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100784', 'abnormal left blastomere', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(312899, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0133305', 'abnormal development of small secretory cell', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312900, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0101638', 'abnormal anatomical structure morphology', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312901, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0133241', 'abnormal development of choroid fissure', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312902, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0133246', 'abnormal development of myocoelic slit', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312903, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0133226', 'abnormal development of hatching gland cell', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312904, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100249', 'abnormal avascular GAG-rich matrix', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312905, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0132373', 'abnormal development of axial mesoderm', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312906, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0141748', 'abnormal gas homeostasis', 0.6666666666666666, 1.4755025719078136, 0.9918005753536725, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312907, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0131472', 'absent vocalization behavior', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312908, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0133216', 'abnormal development of barrier cell', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312909, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100762', 'abnormal intersomitic region', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312910, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0132414', 'abnormal development of basal body', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312911, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0133300', 'abnormal development of skeletal muscle satellite cell', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312912, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0132453', 'abnormal development of myoblast', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312913, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100267', 'abnormal wound epidermis', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312914, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0101575', 'abnormal vitelline membrane', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(312915, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100006', 'abnormal anatomical structure', 0.6153846153846154, 1.4755025719078136, 0.9528911704452407, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312916, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0101468', 'abnormal stage I oocyte', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(312917, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0131698', 'abnormal apical constriction involved in gastrulation', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312918, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0101107', 'abnormal erythroid cell', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(312919, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0141715', 'abnormal septum', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312920, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100205', 'abnormal limb segment', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(312921, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0141787', 'abnormal hormone metabolic process', 0.5555555555555556, 1.8210412618256888, 1.005827813247954, 'HP:0000118', 'Phenotypic abnormality'),
(312922, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0131470', 'abnormal heart contraction', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312923, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0128000', 'absent behavior', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312924, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0133210', 'abnormal development of animal-vegetal axis', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312925, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0101349', 'abnormal trunk region', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312926, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0141776', 'abnormal metabolic process', 0.625, 1.8210412618256888, 1.0668415011804966, 'HP:0000118', 'Phenotypic abnormality'),
(312927, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0141818', 'abnormal peptidoglycan muralytic activity', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312928, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0132589', 'abnormal development of ectodermal cell', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312929, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100989', 'abnormal right blastomere', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(312930, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0141797', 'abnormal hydrogen metabolic process', 0.5555555555555556, 1.8210412618256888, 1.005827813247954, 'HP:0000118', 'Phenotypic abnormality'),
(312931, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0132678', 'abnormal development of proximal tubule branch', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312932, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0101098', 'abnormal mineralized extracellular matrix', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312933, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0131481', 'absent feeding behavior', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312934, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100557', 'abnormal prime meridian', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312935, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0132765', 'abnormal development of hypobranchial placode', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312936, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100156', 'abnormal foregut', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(312937, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100515', 'abnormal somatic stem cell', 0.5263157894736842, 1.8210412618256888, 0.9790009036675816, 'HP:0000118', 'Phenotypic abnormality'),
(312938, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0131714', 'abnormal establishment of tissue polarity', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312939, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100293', 'abnormal duct', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312940, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0133129', 'abnormal development of neurocoel', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312941, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0133401', 'absent determination of left/right symmetry in lateral plate mesoderm', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312942, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0132382', 'abnormal development of presumptive midbrain-hindbrain boundary', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312943, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0101302', 'abnormal subcortical cytoplasm', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(312944, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0131908', 'abnormal development of zygote', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312945, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0107266', 'abnormal dorsal side', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312946, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100277', 'abnormal blastocoel', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312947, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0131730', 'abnormal regulation of protein folding', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312948, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100902', 'abnormal spermatocyte', 0.5263157894736842, 1.8210412618256888, 0.9790009036675816, 'HP:0000118', 'Phenotypic abnormality'),
(312949, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0141878', 'abnormal histamine oxidase activity', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312950, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0141794', 'abnormal prosthetic group metabolic process', 0.5555555555555556, 1.8210412618256888, 1.005827813247954, 'HP:0000118', 'Phenotypic abnormality'),
(312951, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0141497', 'abnormal lymphoblast', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(312952, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100285', 'abnormal progenitor cell', 0.5555555555555556, 1.8210412618256888, 1.005827813247954, 'HP:0000118', 'Phenotypic abnormality'),
(312953, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0132484', 'abnormal development of posterior neural tube', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312954, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0132559', 'abnormal development of anatomical axis', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312955, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100261', 'abnormal multilaminar epithelium', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312956, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0141795', 'abnormal glycosylation', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(312957, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0131804', 'abnormal development of central vegetal yolk mass', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312958, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0132851', 'abnormal development of angioblast', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312959, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0141809', 'abnormal catalytic activity', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312960, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100843', 'abnormal fasciculated network of fibrils', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(312961, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0101553', 'abnormal dental epithelium', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312962, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100415', 'abnormal secretory epithelial cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(312963, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0131764', 'abnormal development of retinal progenitor cell region', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312964, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100429', 'abnormal spermatid', 0.5263157894736842, 1.8210412618256888, 0.9790009036675816, 'HP:0000118', 'Phenotypic abnormality'),
(312965, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0141460', 'abnormal development of lymphoblast', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312966, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0103625', 'absent mitotic cytokinesis in primary spermatogonium', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312967, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0101228', 'abnormal mesenchymal stem cell', 0.5263157894736842, 1.8210412618256888, 0.9790009036675816, 'HP:0000118', 'Phenotypic abnormality'),
(312968, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0101406', 'abnormal cleavage furrow', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312969, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0141962', 'absent cilium motility in pronephric kidney', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312970, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0141266', 'abnormal surface breathing', 0.6666666666666666, 1.4755025719078136, 0.9918005753536725, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312971, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100023', 'abnormal mesenchyme', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312972, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0103444', 'abnormal gastrulation', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312973, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100665', 'abnormal egg jelly', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312974, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100626', 'abnormal primordial germ cell', 0.5263157894736842, 1.8210412618256888, 0.9790009036675816, 'HP:0000118', 'Phenotypic abnormality'),
(312975, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0133037', 'abnormal development of dorsal region', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312976, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0142052', 'abnormal nasal region', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(312977, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0141864', 'abnormal 5-methylcytosine metabolic process', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(312978, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0132194', 'abnormal development of midgut', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312979, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0131786', 'abnormal development of chondrocyte', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312980, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0132430', 'abnormal development of ooplasm', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312981, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100202', 'abnormal embryo', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312982, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0132889', 'abnormal development of dorsal lymph space', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312983, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0141894', 'abnormal dicarboxylic acid transport', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312984, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100289', 'abnormal chondroblast', 0.5555555555555556, 1.8210412618256888, 1.005827813247954, 'HP:0000118', 'Phenotypic abnormality'),
(312985, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100537', 'abnormal medium cavity', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(312986, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0132361', 'abnormal development of dorsal lateral plate mesoderm', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312987, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100481', 'abnormal anatomical line', 0.6153846153846154, 1.4755025719078136, 0.9528911704452407, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312988, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0101023', 'abnormal ultimobranchial body', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(312989, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0141811', 'abnormal oxidoreductase activity', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312990, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0131726', 'abnormal Wnt signaling pathway, planar cell polarity pathway', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312991, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100916', 'abnormal principal cavity', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(312992, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0132400', 'abnormal development of oval window', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312993, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0141799', 'decreased catalytic activity', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312994, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0142010', 'abnormal development of cerebrospinal fluid', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312995, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100707', 'abnormal central vegetal yolk mass', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312996, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100394', 'abnormal marginal zone', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312997, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0132854', 'abnormal development of oral cavity', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312998, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0141975', 'abnormal cilium motility', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(312999, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0133112', 'abnormal development of vegetal cortex', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313000, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0132892', 'abnormal development of M band', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313001, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0131805', 'abnormal development of embryonic structure', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313002, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100402', 'abnormal zeugopod', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(313003, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100664', 'abnormal periocular region', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(313004, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0131814', 'abnormal development of lateral ventricle', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313005, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0132205', 'abnormal development of somatic layer of lateral plate mesoderm', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313006, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100587', 'abnormal vestibuloauditory system', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(313007, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0131731', 'abnormal pigment accumulation in tissues', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313008, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100295', 'abnormal extracellular matrix', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313009, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100540', 'abnormal left lymph heart', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(313010, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0131722', 'abnormal determination of left/right symmetry', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313011, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0101141', 'abnormal Keller explant', 0.5714285714285714, 1.4755025719078136, 0.918228907628411, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313012, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100549', 'abnormal mitotic cell', 0.5555555555555556, 1.8210412618256888, 1.005827813247954, 'HP:0000118', 'Phenotypic abnormality'),
(313013, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0132579', 'abnormal development of hatching gland', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313014, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0132141', 'abnormal development of olfactory pit', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313015, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0132074', 'abnormal development of absorptive cell', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313016, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0132932', 'abnormal development of endothelial cell', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313017, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100059', 'abnormal regenerating tail', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313018, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100754', 'abnormal electrically active cell', 0.5555555555555556, 1.8210412618256888, 1.005827813247954, 'HP:0000118', 'Phenotypic abnormality'),
(313019, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0101109', 'abnormal egg cell-free extract', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313020, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0103624', 'absent anterior/posterior pattern specification in midgut', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313021, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100802', 'abnormal exocrine cell', 0.5555555555555556, 1.8210412618256888, 1.005827813247954, 'HP:0000118', 'Phenotypic abnormality'),
(313022, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100158', 'abnormal neuromere', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(313023, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0131870', 'abnormal development of foregut', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313024, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0101283', 'abnormal left-ventral blastomere', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(313025, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0131940', 'abnormal development of acellular anatomical structure', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313026, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0132858', 'abnormal development of rib', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313027, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100228', 'abnormal skeletal subdivision', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(313028, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0131719', 'abnormal activation of meiosis', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313029, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100745', 'abnormal anterior lymph sac', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(313030, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0101366', 'abnormal morula cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(313031, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0116494', 'absent biological process', 0.6153846153846154, 1.4755025719078136, 0.9528911704452407, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313032, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100915', 'abnormal dermal system', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313033, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0132114', 'abnormal development of ventral endomesoderm', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313034, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0133135', 'abnormal development of medial region', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313035, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0101220', 'abnormal centriole', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(313036, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100872', 'abnormal neuroendocrine cell', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(313037, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0141770', 'abnormal urate homeostasis', 0.6666666666666666, 1.4755025719078136, 0.9918005753536725, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313038, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0132053', 'abnormal development of blood', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313039, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0101240', 'abnormal ciliated non-epidermal cell', 0.5263157894736842, 1.8210412618256888, 0.9790009036675816, 'HP:0000118', 'Phenotypic abnormality'),
(313040, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0132456', 'abnormal development of prime meridian', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313041, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0141881', 'abnormal fructose metabolic process', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(313042, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100268', 'abnormal circulatory system', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313043, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0132485', 'abnormal development of ring structure', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313044, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0141784', 'abnormal cellular hormone metabolic process', 0.6666666666666666, 1.4755025719078136, 0.9918005753536725, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313045, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100135', 'abnormal surface structure', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313046, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100255', 'abnormal pelvic appendage', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313047, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0131703', 'abnormal cell division', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313048, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0101010', 'abnormal dorsal marginal zone', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313049, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0132962', 'abnormal development of female organism', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313050, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100573', 'abnormal extraembryonic structure', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313051, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0141959', 'absent cilium motility in floor plate', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313052, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0101435', 'abnormal paracrine cell', 0.5555555555555556, 1.8210412618256888, 1.005827813247954, 'HP:0000118', 'Phenotypic abnormality'),
(313053, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0131474', 'absent behavioral response to pain', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313054, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0131867', 'abnormal development of antero-dorsal region', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313055, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100867', 'abnormal apical mesenchyme', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313056, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100477', 'abnormal pericyte', 0.5555555555555556, 1.8210412618256888, 1.005827813247954, 'HP:0000118', 'Phenotypic abnormality'),
(313057, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0101497', 'abnormal ciliary axoneme', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(313058, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100384', 'abnormal amputated tissue', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313059, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0133042', 'abnormal development of Roux spot', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313060, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0142057', 'abnormal desmosome', 0.5263157894736842, 1.8210412618256888, 0.9790009036675816, 'HP:0000118', 'Phenotypic abnormality'),
(313061, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100688', 'abnormal adipose tissue', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(313062, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0101113', 'abnormal stage IV oocyte', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(313063, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0103783', 'absent hatching behavior', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313064, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100031', 'abnormal central nervous system', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(313065, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0133297', 'abnormal development of proximal-distal axis', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313066, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0133302', 'abnormal development of growth cone', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313067, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0101450', 'abnormal myeloid cell', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(313068, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0141788', 'abnormal hormone biosynthetic process', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(313069, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0141738', 'abnormal carbon dioxide homeostasis', 0.6666666666666666, 1.4755025719078136, 0.9918005753536725, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313070, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100201', 'abnormal cavitated compound organ', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313071, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0141499', 'abnormal tadpole', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313072, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0131406', 'abnormal social behavior', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313073, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0132257', 'abnormal development of centrosome', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313074, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0133304', 'abnormal development of digit-joint region', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313075, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100207', 'abnormal blastema', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313076, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0131880', 'abnormal development of presumptive rhombomere', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313077, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0132211', 'abnormal development of myofibril', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313078, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0132314', 'abnormal development of splanchnic layer of lateral plate mesoderm', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313079, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0131666', 'abnormal adherens junction', 0.5263157894736842, 1.8210412618256888, 0.9790009036675816, 'HP:0000118', 'Phenotypic abnormality'),
(313080, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0133139', 'abnormal development of apical junction complex', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313081, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100026', 'abnormal germ cell', 0.5555555555555556, 1.8210412618256888, 1.005827813247954, 'HP:0000118', 'Phenotypic abnormality'),
(313082, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0107262', 'abnormal left-right axis', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313083, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0132663', 'abnormal development of pars intermedia', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313084, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100735', 'abnormal hindgut', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(313085, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0141737', 'abnormal carbohydrate homeostasis', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313086, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0141600', 'absent metamorphosis', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313087, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100760', 'abnormal Stirnorgan', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(313088, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0132867', 'abnormal development of myelin accumulating cell', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313089, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0132321', 'abnormal development of epiphysis', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313090, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0141900', 'abnormal mannose metabolic process', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(313091, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100581', 'abnormal immune system', 0.5263157894736842, 1.8210412618256888, 0.9790009036675816, 'HP:0000118', 'Phenotypic abnormality'),
(313092, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100691', 'abnormal keratin accumulating cell', 0.5555555555555556, 1.8210412618256888, 1.005827813247954, 'HP:0000118', 'Phenotypic abnormality'),
(313093, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0101500', 'abnormal endodermal cell', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(313094, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0131694', 'abnormal RNA polymerase II activity', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(313095, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100186', 'abnormal uveal tract', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313096, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100701', 'abnormal microglial cell', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(313097, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100332', 'abnormal germinal granule', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(313098, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0131728', 'abnormal regulation of cell size', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313099, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0131782', 'abnormal development of organism subdivision', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313100, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0131687', 'abnormal astral microtubule', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(313101, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0132599', 'abnormal development of mesodermal cell', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313102, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100599', 'abnormal adult immune system', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(313103, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0132649', 'abnormal development of kinetochore', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313104, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100104', 'abnormal embryonic structure', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313105, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0133069', 'abnormal development of astrocyte end-foot', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313106, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0101136', 'abnormal ooplasm', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(313107, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0101543', 'abnormal external gill', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(313108, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0131409', 'abnormal locomotory behavior', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313109, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0141969', 'absent cilium motility in monociliated cell', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313110, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0133028', 'abnormal development of dorso-lateral region', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313111, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0131983', 'abnormal development of upper blastopore lip', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313112, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0141276', 'decreased surface breathing', 0.6153846153846154, 1.4755025719078136, 0.9528911704452407, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313113, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0132804', 'abnormal development of alkali secreting cell', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313114, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0101402', 'abnormal oropharyngeal papilla', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(313115, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0132317', 'abnormal development of cilium', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313116, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0126321', 'abnormally localised anatomical structure', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313117, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100791', 'abnormal multiciliated cell precursor', 0.5555555555555556, 1.8210412618256888, 1.005827813247954, 'HP:0000118', 'Phenotypic abnormality'),
(313118, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100868', 'abnormal transporting epithelium', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313119, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0133007', 'abnormal development of acinar cell', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313120, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0132787', 'abnormal development of apical region', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313121, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0132668', 'abnormal development of anterior endoderm', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313122, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100742', 'abnormal musculoskeletal system', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313123, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0133184', 'abnormal development of ventro-lateral region', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313124, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100256', 'abnormal paired appendage', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313125, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0141744', 'abnormal chemical homeostasis', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313126, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0141743', 'abnormal chemical homeostasis within a tissue', 0.6666666666666666, 1.4755025719078136, 0.9918005753536725, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313127, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100225', 'abnormal endocrine system', 0.5263157894736842, 1.8210412618256888, 0.9790009036675816, 'HP:0000118', 'Phenotypic abnormality'),
(313128, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0131818', 'abnormal development of mesonephric sinus', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313129, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0131482', 'absent locomotory behavior', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313130, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0133336', 'abnormal development of anterior-posterior axis', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313131, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100781', 'abnormal presumptive ectoderm', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313132, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100799', 'abnormal genital ridge', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(313133, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0132583', 'abnormal development of mitotic cell', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313134, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0132121', 'abnormal development of neuron projection', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313135, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100912', 'abnormal trabecula', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313136, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100377', 'abnormal connective tissue', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(313137, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0101396', 'abnormal apical epithelial cap', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313138, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0132611', 'abnormal development of intercanthal region', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313139, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0132250', 'abnormal development of male organism', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313140, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0132991', 'abnormal development of antero-ventral region', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313141, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100403', 'abnormal forelimb', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(313142, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0127101', 'abnormally localised portion of organism substance', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313143, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0133179', 'abnormal development of mucus secreting cell', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313144, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0131806', 'abnormal development of anatomical system', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313145, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100146', 'abnormal primary germ layer', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313146, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0103445', 'abnormal left/right axis specification', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313147, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100114', 'abnormal peripheral nervous system', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(313148, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0131739', 'abnormal wound healing', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313149, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0131765', 'abnormal development of anatomical region', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313150, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0131725', 'abnormal phosphorylation of RNA polymerase II C-terminal domain', 0.6666666666666666, 1.4755025719078136, 0.9918005753536725, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313151, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0133388', 'absent insulin receptor signaling pathway', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313152, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0133060', 'abnormal development of zygote cortex', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313153, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100444', 'abnormal cement gland', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313154, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0131744', 'abnormal apical constriction', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313155, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0132056', 'abnormal development of eye photoreceptor cell', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313156, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0141736', 'abnormal anatomical structure homeostasis', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313157, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0133295', 'abnormal development of peripheral vegetal yolk mass', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313158, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0115391', 'abnormally undifferentiated alimentary system', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(313159, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0141960', 'absent cilium motility in brain', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313160, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0131875', 'abnormal development of dorsal endomesoderm', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313161, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0101326', 'abnormal cementoblast', 0.5555555555555556, 1.8210412618256888, 1.005827813247954, 'HP:0000118', 'Phenotypic abnormality'),
(313162, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0132865', 'abnormal development of lateral nasal prominence', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313163, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100282', 'abnormal pelvic girdle primordium', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313164, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100588', 'abnormal unicellular gland', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313165, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0103447', 'abnormal anterior/posterior axis specification', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313166, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0133331', 'abnormal development of osteoblast', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313167, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100187', 'abnormal regenerating limb', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313168, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0101347', 'abnormal hindlimb region', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313169, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0131704', 'abnormal cell migration', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313170, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0141841', 'abnormality of whole organism mass', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(313171, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0132410', 'abnormal development of anterior region', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313172, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0131477', 'absent visual behavior', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313173, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0141798', 'abnormal lipid metabolic process', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(313174, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0141271', 'increased surface breathing', 0.6153846153846154, 1.4755025719078136, 0.9528911704452407, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313175, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0132977', 'abnormal development of neuromast mantle cell', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313176, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0101569', 'abnormal activin-induced ectoderm', 0.5714285714285714, 1.4755025719078136, 0.918228907628411, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313177, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100574', 'abnormal gastrula cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(313178, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100258', 'abnormal organ part', 0.5714285714285714, 1.4755025719078136, 0.918228907628411, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313179, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0141775', 'abnormal nitrogen compound metabolic process', 0.5555555555555556, 1.8210412618256888, 1.005827813247954, 'HP:0000118', 'Phenotypic abnormality'),
(313180, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0101573', 'abnormal peripheral vegetal yolk mass', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313181, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0101072', 'abnormal mitochondrial cloud', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(313182, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100093', 'abnormal simple squamous epithelium', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313183, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0131798', 'abnormal development of anatomical space', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313184, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0101264', 'abnormal mitotic spindle', 0.5263157894736842, 1.8210412618256888, 0.9790009036675816, 'HP:0000118', 'Phenotypic abnormality'),
(313185, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0101133', 'abnormal motor neuron', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(313186, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0101519', 'abnormal hypobranchial placode', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313187, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0141813', 'abnormal hydrolase activity', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313188, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0132927', 'abnormal development of central retina', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313189, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0141967', 'absent cilium motility in esophagus', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313190, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0132162', 'abnormal development of principal cavity', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313191, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100523', 'abnormal midgut', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(313192, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0132986', 'abnormal development of vegetal pole', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313193, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0141817', 'abnormal demethylase activity', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313194, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0132762', 'abnormal development of blastocoel', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313195, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0133328', 'abnormal development of animal pole', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313196, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0101269', 'abnormal mesodermal cell', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(313197, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0142016', 'abnormal development of desmosome', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313198, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0101461', 'abnormal sperm entry point', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(313199, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0107258', 'abnormal anatomical axis', 0.5714285714285714, 1.4755025719078136, 0.918228907628411, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313200, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100081', 'abnormal anatomical entity in vitro', 0.6153846153846154, 1.4755025719078136, 0.9528911704452407, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313201, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0132098', 'abnormal development of organ part', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313202, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0125007', 'absent anatomical line', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313203, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0132316', 'abnormal development of migratory neural crest cell', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313204, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0132607', 'abnormal development of microtubule', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313205, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0101587', 'abnormal hemangioblast', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(313206, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100189', 'abnormal enteroendocrine cell', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(313207, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0132695', 'abnormal development of posterior endomesoderm', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313208, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0131399', 'abnormal vocalization behavior', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313209, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100724', 'abnormal kinetochore', 0.5263157894736842, 1.8210412618256888, 0.9790009036675816, 'HP:0000118', 'Phenotypic abnormality'),
(313210, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0132150', 'abnormal development of lampbrush chromosome', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313211, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0101389', 'abnormal wedge region', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(313212, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0132455', 'abnormal development of diaphysis', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313213, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0101004', 'abnormal acid secreting cell', 0.5555555555555556, 1.8210412618256888, 1.005827813247954, 'HP:0000118', 'Phenotypic abnormality'),
(313214, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100509', 'abnormal germ plasm', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(313215, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100715', 'abnormal ciliated cell', 0.5555555555555556, 1.8210412618256888, 1.005827813247954, 'HP:0000118', 'Phenotypic abnormality'),
(313216, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0141778', 'abnormal biosynthetic process', 0.5555555555555556, 1.8210412618256888, 1.005827813247954, 'HP:0000118', 'Phenotypic abnormality'),
(313217, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100610', 'abnormal appendage', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313218, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0107278', 'abnormal medial region', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313219, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0101074', 'abnormal germinal vesicle', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(313220, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0101174', 'abnormal articular system', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(313221, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0131473', 'absent courtship behavior', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313222, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0115509', 'abnormally semi-viable whole organism', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313223, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0107261', 'abnormal dorsal-ventral axis', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313224, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0133228', 'abnormal development of dorsolateral neural tube', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313225, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0131469', 'abnormal heart process', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313226, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0101713', 'abnormal anatomical entity in vitro morphology', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313227, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0133054', 'abnormal development of digestive enzyme secreting cell', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313228, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0132577', 'abnormal development of oral evagination', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313229, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100398', 'abnormal vegetal blastomere', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(313230, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0141791', 'abnormal primary metabolic process', 0.5555555555555556, 1.8210412618256888, 1.005827813247954, 'HP:0000118', 'Phenotypic abnormality'),
(313231, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0131926', 'abnormal development of germ cell', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313232, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0141850', 'abnormal galactose metabolic process', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(313233, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100172', 'abnormal stem cell', 0.5555555555555556, 1.8210412618256888, 1.005827813247954, 'HP:0000118', 'Phenotypic abnormality'),
(313234, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100232', 'abnormal lymphatic system', 0.5263157894736842, 1.8210412618256888, 0.9790009036675816, 'HP:0000118', 'Phenotypic abnormality'),
(313235, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0132953', 'abnormal development of thoracic region', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313236, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100612', 'abnormal unilaminar epithelium', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313237, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0133090', 'abnormal development of fenestra subocularis', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313238, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100274', 'abnormal sensory system', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(313239, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0131912', 'abnormal development of premigratory neural crest cell', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313240, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100935', 'abnormal skeleton', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(313241, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0101570', 'abnormal forelimb region', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313242, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0101224', 'abnormal dorsal involuting marginal zone', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313243, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0133049', 'abnormal development of anterior entopeduncular region', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313244, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0141725', 'increased catalytic activity', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313245, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0132823', 'abnormal development of basal region', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313246, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100028', 'abnormal anatomical cluster', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313247, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100468', 'abnormal muscular system', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313248, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100003', 'abnormal organism subdivision', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313249, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0141908', 'abnormal pyridine metabolic process', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(313250, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100296', 'abnormal tail region', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313251, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0142056', 'abnormal main body axis', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313252, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0132376', 'abnormal development of third ventricle', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313253, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0141871', 'abnormal cadaverine transport', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313254, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0131833', 'abnormal development of cell part', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313255, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0101976', 'abnormal portion of organism substance morphology', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313256, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100727', 'abnormal odontogenic papilla', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(313257, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0101221', 'abnormal larval immune system', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(313258, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0141880', 'abnormal ethanolamine metabolic process', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(313259, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0141767', 'abnormal temperature homeostasis', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(313260, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0101212', 'abnormal glomeral mesenchyme', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(313261, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0101501', 'abnormal parabrachial area', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(313262, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0116429', 'abnormal behavior', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313263, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100917', 'abnormal stage III oocyte', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(313264, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100907', 'abnormal cytoplasm', 0.5263157894736842, 1.8210412618256888, 0.9790009036675816, 'HP:0000118', 'Phenotypic abnormality'),
(313265, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0115758', 'abnormally decreased mobility of melanoblast', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(313266, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100308', 'abnormal early embryonic cell', 0.5263157894736842, 1.8210412618256888, 0.9790009036675816, 'HP:0000118', 'Phenotypic abnormality'),
(313267, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0132853', 'abnormal development of stromal cell', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313268, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100640', 'abnormal notochordal sheath', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(313269, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0132940', 'abnormal development of follicle cell', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313270, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0101409', 'abnormal perivitelline space', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(313271, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0132161', 'abnormal development of animal cap', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313272, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0131475', 'absent olfactory behavior', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313273, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0141796', 'abnormal demethylation', 0.5555555555555556, 1.8210412618256888, 1.005827813247954, 'HP:0000118', 'Phenotypic abnormality'),
(313274, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0132133', 'abnormal development of circulating cell', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313275, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0133171', 'abnormal development of germinal granule', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313276, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0102113', 'abnormal anatomical line morphology', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313277, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0133098', 'abnormal development of Brachets cleft', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313278, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0101333', 'abnormal barrier epithelial cell', 0.5555555555555556, 1.8210412618256888, 1.005827813247954, 'HP:0000118', 'Phenotypic abnormality'),
(313279, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0141792', 'abnormal small molecule metabolic process', 0.5555555555555556, 1.8210412618256888, 1.005827813247954, 'HP:0000118', 'Phenotypic abnormality'),
(313280, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0141859', 'abnormal lactose catabolic process', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(313281, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100702', 'abnormal glial cell', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(313282, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0133096', 'abnormal development of paracrine cell', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313283, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0132391', 'abnormal development of ciliated cell', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313284, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100585', 'abnormal elastica externa', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(313285, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0132557', 'abnormal development of filopodium', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313286, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0131756', 'abnormal development of vegetal yolk mass', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313287, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0101200', 'abnormal joint region', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313288, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100176', 'abnormal stage VI oocyte', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(313289, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0141898', 'abnormal maltose metabolic process', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(313290, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0132710', 'abnormal development of polar body', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313291, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100376', 'abnormal animal pole', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313292, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0107339', 'abnormal yolk platelet', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(313293, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100741', 'abnormal blastopore', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313294, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0133101', 'abnormal development of acid secreting cell', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313295, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0132496', 'abnormal development of left-right organizer', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313296, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0131715', 'abnormal fibroblast growth factor receptor signaling pathway', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313297, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0132044', 'abnormal development of marginal zone', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313298, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0141907', 'abnormal putrescine metabolic process', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(313299, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0107269', 'abnormal right side', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313300, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0132645', 'abnormal development of ventral foregut', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313301, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0141958', 'absent cilium motility in left-right organizer', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313302, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0132231', 'abnormal development of actin cytoskeleton', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313303, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0132192', 'abnormal development of prechordal plate', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313304, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0141872', 'abnormal cholesterol metabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(313305, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0141461', 'abnormal development of axon microtubule bundle', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313306, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0132658', 'abnormal development of ventral endoderm', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313307, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0132808', 'abnormal development of medium cavity', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313308, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100392', 'abnormal cilium', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(313309, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100120', 'abnormal genital system', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(313310, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0133153', 'abnormal development of exocrine cell', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313311, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0107272', 'abnormal axial region', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313312, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0115473', 'abnormally delayed phase of Mullerian duct', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(313313, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0133203', 'abnormal development of ventral region', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313314, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100553', 'abnormal laryngeal muscle primordium', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313315, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0141724', 'abnormal prevention of polyspermy', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313316, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0101448', 'abnormal myelin accumulating cell', 0.5555555555555556, 1.8210412618256888, 1.005827813247954, 'HP:0000118', 'Phenotypic abnormality'),
(313317, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0131700', 'abnormal BMP signaling pathway', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313318, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100531', 'abnormal proliferative region', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313319, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0132199', 'abnormal development of blastopore', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313320, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0101377', 'abnormal manicotto glandulare', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(313321, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0101263', 'abnormal blastocoel floor', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313322, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0131471', 'absent swimming behavior', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313323, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0107326', 'abnormal regenerating pelvic girdle', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313324, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100417', 'abnormal dense regular connective tissue', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(313325, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100032', 'abnormal nervous system', 0.5263157894736842, 1.8210412618256888, 0.9790009036675816, 'HP:0000118', 'Phenotypic abnormality'),
(313326, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0133109', 'abnormal development of plasma membrane', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313327, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100991', 'abnormal iliac process primordium', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313328, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0132755', 'abnormal development of mitochondrial cloud', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313329, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0141789', 'abnormal hormone catabolic process', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(313330, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100816', 'abnormal blastocoel anlage', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313331, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0141904', 'abnormal glucosamine metabolic process', 0.5555555555555556, 1.8210412618256888, 1.005827813247954, 'HP:0000118', 'Phenotypic abnormality'),
(313332, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100860', 'abnormal parathyroid', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(313333, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100852', 'abnormal interdigital region', 0.5555555555555556, 1.8210412618256888, 1.005827813247954, 'HP:0000118', 'Phenotypic abnormality'),
(313334, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0131975', 'abnormal development of anatomical line', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313335, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0133120', 'abnormal development of multiciliated cell precursor', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313336, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0141910', 'abnormal D-ribose metabolic process', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(313337, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100900', 'abnormal angioblast', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(313338, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0133001', 'abnormal development of wedge region', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313339, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0133087', 'abnormal development of neuromast support cell', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313340, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0132367', 'abnormal development of melanotrope', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313341, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100894', 'abnormal nucleus', 0.5263157894736842, 1.8210412618256888, 0.9790009036675816, 'HP:0000118', 'Phenotypic abnormality'),
(313342, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0133260', 'abnormal development of posterior region', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313343, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0131916', 'abnormal development of myocyte', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313344, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0132995', 'abnormal development of barrier epithelial cell', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313345, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100363', 'abnormal cardiovascular system', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313346, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100728', 'abnormal cell condensation', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313347, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0131738', 'abnormal Wnt signaling pathway', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313348, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100638', 'abnormal polar body', 0.5555555555555556, 1.8210412618256888, 1.005827813247954, 'HP:0000118', 'Phenotypic abnormality'),
(313349, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0131479', 'absent social behavior', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313350, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100383', 'abnormal amputated fin', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313351, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0131745', 'abnormal axis elongation', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(313352, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0132057', 'abnormal development of circumblastoporal collar', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313353, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0133395', 'abnormal determination of left/right symmetry in alimentary system', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313354, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0141265', 'abnormal escape behavior', 0.6666666666666666, 1.4755025719078136, 0.9918005753536725, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313355, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0132446', 'abnormal development of midbrain-hindbrain boundary', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313356, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0132996', 'abnormal development of ventricular zone', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313357, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0116091', 'abnormally increased variability of size of cell in endoderm', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(313358, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100842', 'abnormal left-dorsal blastomere', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(313359, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0132249', 'abnormal development of whole organism', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313360, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0101029', 'abnormal right spleen primordium', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(313361, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100546', 'abnormal whole organism', 0.5714285714285714, 1.4755025719078136, 0.918228907628411, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313362, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0133263', 'abnormal development of yolk platelet', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313363, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0133402', 'absent determination of left/right symmetry in alimentary system', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313364, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0141267', 'abnormal resting posture', 0.6666666666666666, 1.4755025719078136, 0.9918005753536725, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313365, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0131836', 'abnormal development of glial cell', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313366, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0132501', 'abnormal development of marginal zone (sensu neural)', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313367, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0132716', 'abnormal development of centriole', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313368, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0133325', 'abnormal development of postero-dorsal region', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313369, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100888', 'abnormal microtubule', 0.5263157894736842, 1.8210412618256888, 0.9790009036675816, 'HP:0000118', 'Phenotypic abnormality'),
(313370, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0141852', 'abnormal glucose metabolic process', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(313371, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100864', 'abnormal dorsolateral ascending neuron', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(313372, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0101132', 'abnormal apoptotic cell', 0.5555555555555556, 1.8210412618256888, 1.005827813247954, 'HP:0000118', 'Phenotypic abnormality'),
(313373, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0133215', 'abnormal development of adherens junction', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313374, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0141771', 'abnormal urea homeostasis', 0.6666666666666666, 1.4755025719078136, 0.9918005753536725, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313375, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0103446', 'abnormal proximal/distal axis specification', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313376, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0101297', 'abnormal barrier cell', 0.5555555555555556, 1.8210412618256888, 1.005827813247954, 'HP:0000118', 'Phenotypic abnormality'),
(313377, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100899', 'abnormal secondary spermatogonium', 0.5263157894736842, 1.8210412618256888, 0.9790009036675816, 'HP:0000118', 'Phenotypic abnormality'),
(313378, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0131891', 'abnormal development of anterior neural tube', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313379, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100273', 'abnormal visual system', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(313380, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0131723', 'abnormal pathway-restricted SMAD protein phosphorylation', 0.6666666666666666, 1.4755025719078136, 0.9918005753536725, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313381, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0132839', 'abnormal development of perichondrial cell', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313382, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100796', 'abnormal pseudoblastema', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313383, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0131740', 'abnormal detection of nodal flow', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313384, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0132935', 'abnormal development of circumpharyngeal ridge', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313385, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0101480', 'abnormal stage V oocyte', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(313386, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100616', 'abnormal ventral blood island', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(313387, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100974', 'abnormal cardiac mesoderm', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313388, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100722', 'abnormal barbel', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313389, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0101110', 'abnormal cell-free extract', 0.5714285714285714, 1.4755025719078136, 0.918228907628411, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313390, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0141315', 'abnormal anatomical region', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313391, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0101078', 'abnormal mucous gland', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313392, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0132073', 'abnormal development of presumptive ectoderm', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313393, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0131859', 'abnormal development of ventrolateral neural tube', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313394, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0107263', 'abnormal anatomical side', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313395, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0101092', 'abnormal dorso-lateral marginal zone', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313396, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100152', 'abnormal alimentary system', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(313397, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100422', 'abnormal notochord', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(313398, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0101740', 'abnormal cell part morphology', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(313399, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0101424', 'abnormal coelomic epithelium', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313400, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0107260', 'abnormal anterior-posterior axis', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313401, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0141786', 'abnormal pigment metabolic process', 0.5555555555555556, 1.8210412618256888, 1.005827813247954, 'HP:0000118', 'Phenotypic abnormality'),
(313402, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0131936', 'abnormal development of brain ventricle', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313403, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100969', 'abnormal disaggregated/reaggregated ectoderm treated with activin', 0.5714285714285714, 1.4755025719078136, 0.918228907628411, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313404, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0107270', 'abnormal proximal-distal axis', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313405, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0131741', 'abnormal convergent extension', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313406, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0132403', 'abnormal development of cell condensation', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313407, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0132979', 'abnormal development of presumptive paraxial mesoderm', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313408, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0132999', 'abnormal development of secondary myofiber', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313409, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0132614', 'abnormal development of Merkel cell', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313410, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0131742', 'abnormal axon extension involved in regeneration', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(313411, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0132906', 'abnormal development of optic disc', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313412, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0101577', 'abnormal notochordal epithelium', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313413, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0132587', 'abnormal development of keratin accumulating cell', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313414, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100734', 'abnormal lateral line system', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(313415, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0101040', 'abnormal axial mesoderm', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313416, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0101411', 'abnormal marginal zone (sensu neural)', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313417, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0141971', 'absent cilium motility in ciliated epidermal cell', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313418, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0132733', 'abnormal development of filter chamber', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313419, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0126624', 'abnormally localised anatomical line', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313420, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0133392', 'abnormal cysteine-type endopeptidase activity', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313421, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100786', 'abnormal presumptive axial mesoderm', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313422, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0141966', 'absent cilium motility in stomach', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313423, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0133163', 'abnormal development of nucleate erythrocyte', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313424, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0133067', 'abnormal development of vegetal endoderm', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313425, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0131778', 'abnormal development of primordium', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313426, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0132861', 'abnormal development of pericyte', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313427, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0141264', 'abnormal schooling behavior', 0.6666666666666666, 1.4755025719078136, 0.9918005753536725, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313428, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100004', 'abnormal cell', 0.5882352941176471, 1.8210412618256888, 1.034988281214046, 'HP:0000118', 'Phenotypic abnormality'),
(313429, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0131691', 'abnormal molecular function', 0.6153846153846154, 1.4755025719078136, 0.9528911704452407, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313430, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0131675', 'abnormal spindle microtubule', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(313431, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0132899', 'abnormal development of glomeral mesenchyme', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313432, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100309', 'abnormal vegetal hemisphere', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313433, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0101162', 'abnormal stromal cell', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(313434, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100807', 'abnormal matrix-based tissue', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313435, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0101451', 'abnormal dorsal lymph space', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(313436, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0132091', 'abnormal development of intersomitic region', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313437, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0141263', 'abnormal visually guided collision avoidance behavior', 0.6666666666666666, 1.4755025719078136, 0.9918005753536725, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313438, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0101362', 'abnormal vegetal cortex', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(313439, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0107253', 'abnormal enteric nervous system', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(313440, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100151', 'abnormal primordium', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313441, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0101368', 'abnormal regenerating eye', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313442, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0101071', 'abnormal endoplasmic reticulum', 0.5263157894736842, 1.8210412618256888, 0.9790009036675816, 'HP:0000118', 'Phenotypic abnormality'),
(313443, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100231', 'abnormal compound organ', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313444, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0131942', 'abnormal development of dorsal endoderm', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313445, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0132299', 'abnormal development of epicardial precursor cell', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313446, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0133077', 'abnormal development of mitotic spindle', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313447, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100060', 'abnormal regenerating tissue', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313448, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0131904', 'abnormal development of lymphocyte', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313449, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100985', 'abnormal simple columnar epithelium', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313450, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0131755', 'abnormal development of tissue', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313451, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0132702', 'abnormal development of oxygen accumulating cell', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313452, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0133206', 'abnormal development of hemangioblast', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313453, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100846', 'abnormal hindlimb', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(313454, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0132528', 'abnormal development of sarcomere', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313455, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100887', 'abnormal right-dorsal blastomere', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(313456, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0132876', 'abnormal development of endodermal cell', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313457, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0131973', 'abnormal development of anterior foregut', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313458, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0131721', 'abnormal nodal signaling pathway', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313459, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0141781', 'abnormal secondary metabolic process', 0.5555555555555556, 1.8210412618256888, 1.005827813247954, 'HP:0000118', 'Phenotypic abnormality'),
(313460, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0132052', 'abnormal development of trunk placode', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313461, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0101149', 'abnormal amputated limb', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313462, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0132920', 'abnormal development of olfactory epithelial support cell', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313463, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0132624', 'abnormal development of migrating neuroblast', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313464, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0141783', 'abnormal collagen metabolic process', 0.5555555555555556, 1.8210412618256888, 1.005827813247954, 'HP:0000118', 'Phenotypic abnormality'),
(313465, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100890', 'abnormal pharyngeal cavity', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(313466, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0131685', 'abnormal cortical actin cytoskeleton', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(313467, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100627', 'abnormal pharyngeal region', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(313468, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0101463', 'abnormal right-ventral blastomere', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(313469, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100449', 'abnormal lymphocyte', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(313470, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0132635', 'abnormal development of medial nasal prominence', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313471, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0107284', 'abnormal migrating myoblast', 0.5263157894736842, 1.8210412618256888, 0.9790009036675816, 'HP:0000118', 'Phenotypic abnormality'),
(313472, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100203', 'abnormal endocrine cell', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(313473, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100133', 'abnormal solid compound organ', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313474, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0132706', 'abnormal development of cortical actin cytoskeleton', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313475, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100437', 'abnormal proepicardium', 0.5263157894736842, 1.8210412618256888, 0.9790009036675816, 'HP:0000118', 'Phenotypic abnormality'),
(313476, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0133254', 'abnormal development of ligament cell', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313477, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100458', 'abnormal autopod', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(313478, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0132585', 'abnormal development of pharyngeal cavity', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313479, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100856', 'abnormal simple organ', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313480, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0131476', 'absent mechanosensory behavior', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313481, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100317', 'abnormal respiratory system', 0.5263157894736842, 1.8210412618256888, 0.9790009036675816, 'HP:0000118', 'Phenotypic abnormality'),
(313482, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0141965', 'absent cilium motility in alimentary system', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313483, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0131986', 'abnormal development of hindgut', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313484, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0132558', 'abnormal development of dorsal-ventral axis', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313485, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0131990', 'abnormal development of progenitor cell', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313486, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0101503', 'abnormal organ cortex', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313487, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0107267', 'abnormal ventral side', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313488, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0131807', 'abnormal development of anatomical group', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313489, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0131757', 'abnormal development of multicellular anatomical structure', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313490, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100103', 'abnormal trunk', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313491, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0141911', 'abnormal ribose phosphate metabolic process', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(313492, 'HP:0000118', 'Phenotypic abnormality', 'XPO:00000000', 'Xenopus phenotype', 0.7272727272727273, 1.4755025719078136, 1.0359019159984786, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313493, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0101168', 'abnormal circulating cell', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(313494, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100100', 'abnormal muscle', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(313495, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100378', 'abnormal perichondrium', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(313496, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0133276', 'abnormal development of forelimb region', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313497, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100337', 'abnormal zygote', 0.5555555555555556, 1.8210412618256888, 1.005827813247954, 'HP:0000118', 'Phenotypic abnormality'),
(313498, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0132347', 'abnormal development of myeloid cell', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313499, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0101533', 'abnormal simple cuboidal epithelium', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313500, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100704', 'abnormal Merkel cell', 0.5555555555555556, 1.8210412618256888, 1.005827813247954, 'HP:0000118', 'Phenotypic abnormality'),
(313501, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100009', 'abnormal multi-tissue structure', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313502, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0132491', 'abnormal development of apoptotic cell', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313503, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0141883', 'abnormal glycerol metabolic process', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(313504, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0133213', 'abnormal development of fenestra basicranialis', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313505, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0133074', 'abnormal development of ciliary axoneme', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313506, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100482', 'abnormal Mullerian duct', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(313507, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0141972', 'absent cilium motility in ciliated non-epidermal cell', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313508, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0132181', 'abnormal development of germ plasm', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313509, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100108', 'abnormal cell part', 0.5555555555555556, 1.8210412618256888, 1.005827813247954, 'HP:0000118', 'Phenotypic abnormality'),
(313510, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0133286', 'abnormal development of erythroid cell', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313511, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0131871', 'abnormal development of embryo', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313512, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0141854', 'abnormal glutathione metabolic process', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(313513, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100653', 'abnormal myoblast', 0.5555555555555556, 1.8210412618256888, 1.005827813247954, 'HP:0000118', 'Phenotypic abnormality'),
(313514, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0101547', 'abnormal lampbrush chromosome', 0.5263157894736842, 1.8210412618256888, 0.9790009036675816, 'HP:0000118', 'Phenotypic abnormality'),
(313515, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0131921', 'abnormal development of endocrine cell', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313516, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100954', 'abnormal neural progenitor cell', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(313517, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0116434', 'abnormal biological process', 0.6153846153846154, 1.4755025719078136, 0.9528911704452407, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313518, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0101589', 'abnormal blastocoel roof', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313519, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100002', 'abnormal head', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(313520, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0101405', 'abnormal ring structure', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(313521, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0133131', 'abnormal development of axial region', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313522, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100511', 'abnormal stylopod', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(313523, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100433', 'abnormal pectoral appendage', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313524, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0141754', 'abnormal homeostatic process', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313525, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0133136', 'abnormal development of podocyte', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313526, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0132270', 'abnormal development of postmigratory neural crest cell', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313527, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0131760', 'abnormal development of anatomical structure', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313528, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0132836', 'abnormal development of transverse process', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313529, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0133394', 'abnormal determination of left/right symmetry in lateral plate mesoderm', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313530, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0107285', 'abnormal flexural organ', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(313531, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0115566', 'abnormal variability of size of forelimb', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(313532, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100726', 'abnormal tail', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313533, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0101498', 'abnormal stage II oocyte', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(313534, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100070', 'abnormal anatomical system', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313535, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0132550', 'abnormal development of interdigital region', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313536, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100605', 'abnormal prechordal plate', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313537, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0101490', 'abnormal ectodermal cell', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(313538, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100913', 'abnormal Brachets cleft', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313539, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0141597', 'abnormal metamorphosis', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313540, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0101378', 'abnormal blastomere D1', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(313541, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100084', 'abnormal anatomical group', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313542, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0103443', 'abnormal dorsal/ventral axis specification', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313543, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0133142', 'abnormal development of electrically active cell', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313544, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100687', 'abnormal periotic region', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(313545, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0141961', 'absent cilium motility in mucociliary epithelium', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313546, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0101099', 'abnormal ventro-lateral marginal zone', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313547, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0132942', 'abnormal development of iliac process', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313548, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0101460', 'abnormal fibrocellular pad', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313549, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0132911', 'abnormal development of posterior foregut', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313550, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0133397', 'abnormal insulin receptor signaling pathway', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313551, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0132006', 'abnormal development of extraembryonic structure', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313552, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100643', 'abnormal thoracic region', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313553, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0141970', 'absent cilium motility in multiciliated cell', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313554, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100854', 'abnormal spiracle', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313555, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100486', 'abnormal oral evagination', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(313556, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0141903', 'abnormal inositol phosphate metabolic process', 0.43478260869565216, 1.8210412618256888, 0.8898073220416851, 'HP:0000118', 'Phenotypic abnormality'),
(313557, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100545', 'abnormal male organism', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313558, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100386', 'abnormal limb', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(313559, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0133076', 'abnormal development of buccopharyngeal membrane', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313560, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100344', 'abnormal portion of organism substance', 0.6153846153846154, 1.4755025719078136, 0.9528911704452407, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313561, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0132943', 'abnormal development of left-right axis', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313562, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0116433', 'abnormal axis specification', 0.5, 1.4755025719078136, 0.8589244937443028, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313563, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0141815', 'abnormal isomerase activity', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313564, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0132567', 'abnormal development of retinal stem cell region', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313565, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100162', 'abnormal presumptive rhombomere', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313566, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0131705', 'abnormal chemotaxis', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313567, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0115505', 'dead whole organism', 0.5333333333333333, 1.4755025719078136, 0.8870934026456857, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313568, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0131861', 'abnormal development of thrombocyte', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313569, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0101057', 'abnormal vegetal pole', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313570, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0132346', 'abnormal development of ventral mesoderm', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313571, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0141714', 'abnormal anterior notochord', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(313572, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100192', 'abnormal epithelium', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313573, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0131701', 'abnormal calcium ion transport', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313574, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0132372', 'abnormal development of cleavage furrow', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313575, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0132547', 'abnormal development of pial cell', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313576, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0131961', 'abnormal development of epithelial cell', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313577, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100465', 'abnormal skeletal system', 0.47619047619047616, 1.8210412618256888, 0.9312156064152277, 'HP:0000118', 'Phenotypic abnormality'),
(313578, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0132054', 'abnormal development of portion of organism substance', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313579, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0132280', 'abnormal development of chondroblast', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313580, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0131402', 'abnormal olfactory behavior', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313581, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0100339', 'abnormal circumblastoporal collar', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313582, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0124719', 'absent anatomical structure', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313583, 'HP:0000118', 'Phenotypic abnormality', 'XPO:0101061', 'abnormal plasma membrane', 0.5263157894736842, 1.8210412618256888, 0.9790009036675816, 'HP:0000118', 'Phenotypic abnormality'),
(313584, 'HP:0200024', 'Premature chromatid separation', 'XPO:0101497', 'abnormal ciliary axoneme', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(313585, 'HP:0200024', 'Premature chromatid separation', 'XPO:0100691', 'abnormal keratin accumulating cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(313586, 'HP:0200024', 'Premature chromatid separation', 'XPO:0100899', 'abnormal secondary spermatogonium', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(313587, 'HP:0200024', 'Premature chromatid separation', 'XPO:0101071', 'abnormal endoplasmic reticulum', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(313588, 'HP:0200024', 'Premature chromatid separation', 'XPO:0100842', 'abnormal left-dorsal blastomere', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(313589, 'HP:0200024', 'Premature chromatid separation', 'XPO:0100956', 'abnormal centrosome', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(313590, 'HP:0200024', 'Premature chromatid separation', 'XPO:0131720', 'abnormal mitotic spindle assembly', 0.5555555555555556, 10.281312506061912, 2.389945664893976, 'HP:0002916', 'Abnormality of chromosome segregation'),
(313591, 'HP:0200024', 'Premature chromatid separation', 'XPO:0135474', 'increased cell population proliferation in anatomical structure', 0.425, 5.835653092541957, 1.5748500132807353, 'HP:0011017', 'Abnormal cellular physiology'),
(313592, 'HP:0200024', 'Premature chromatid separation', 'XPO:0138581', 'decreased cell population proliferation in male organism', 0.40476190476190477, 5.835653092541957, 1.5368962428436679, 'HP:0011017', 'Abnormal cellular physiology'),
(313593, 'HP:0200024', 'Premature chromatid separation', 'XPO:0100887', 'abnormal right-dorsal blastomere', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(313594, 'HP:0200024', 'Premature chromatid separation', 'XPO:0131669', 'abnormal Roux spot', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(313595, 'HP:0200024', 'Premature chromatid separation', 'XPO:0100515', 'abnormal somatic stem cell', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(313596, 'HP:0200024', 'Premature chromatid separation', 'XPO:0101283', 'abnormal left-ventral blastomere', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(313597, 'HP:0200024', 'Premature chromatid separation', 'XPO:0101366', 'abnormal morula cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(313598, 'HP:0200024', 'Premature chromatid separation', 'XPO:0135160', 'increased cell population proliferation in embryo', 0.40476190476190477, 5.835653092541957, 1.5368962428436679, 'HP:0011017', 'Abnormal cellular physiology'),
(313599, 'HP:0200024', 'Premature chromatid separation', 'XPO:0107339', 'abnormal yolk platelet', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(313600, 'HP:0200024', 'Premature chromatid separation', 'XPO:0101333', 'abnormal barrier epithelial cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(313601, 'HP:0200024', 'Premature chromatid separation', 'XPO:0101547', 'abnormal lampbrush chromosome', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(313602, 'HP:0200024', 'Premature chromatid separation', 'XPO:0135718', 'increased cell population proliferation in anatomical line', 0.425, 5.835653092541957, 1.5748500132807353, 'HP:0011017', 'Abnormal cellular physiology'),
(313603, 'HP:0200024', 'Premature chromatid separation', 'XPO:0141438', 'increased cell population proliferation in tadpole', 0.40476190476190477, 5.835653092541957, 1.5368962428436679, 'HP:0011017', 'Abnormal cellular physiology'),
(313604, 'HP:0200024', 'Premature chromatid separation', 'XPO:0101467', 'abnormal alkali secreting cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(313605, 'HP:0200024', 'Premature chromatid separation', 'XPO:0135736', 'increased cell population proliferation in cell condensation', 0.40476190476190477, 5.835653092541957, 1.5368962428436679, 'HP:0011017', 'Abnormal cellular physiology'),
(313606, 'HP:0200024', 'Premature chromatid separation', 'XPO:0135478', 'increased cell population proliferation in female organism', 0.40476190476190477, 5.835653092541957, 1.5368962428436679, 'HP:0011017', 'Abnormal cellular physiology'),
(313607, 'HP:0200024', 'Premature chromatid separation', 'XPO:0131667', 'abnormal actin cytoskeleton', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(313608, 'HP:0200024', 'Premature chromatid separation', 'XPO:0100894', 'abnormal nucleus', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(313609, 'HP:0200024', 'Premature chromatid separation', 'XPO:0142057', 'abnormal desmosome', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(313610, 'HP:0200024', 'Premature chromatid separation', 'XPO:0138717', 'decreased cell population proliferation in acellular anatomical structure', 0.40476190476190477, 5.835653092541957, 1.5368962428436679, 'HP:0011017', 'Abnormal cellular physiology'),
(313611, 'HP:0200024', 'Premature chromatid separation', 'XPO:0100285', 'abnormal progenitor cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(313612, 'HP:0200024', 'Premature chromatid separation', 'XPO:0100533', 'abnormal melanoblast', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(313613, 'HP:0200024', 'Premature chromatid separation', 'XPO:0100549', 'abnormal mitotic cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(313614, 'HP:0200024', 'Premature chromatid separation', 'XPO:0139423', 'decreased cell population proliferation in multicellular anatomical structure', 0.40476190476190477, 5.835653092541957, 1.5368962428436679, 'HP:0011017', 'Abnormal cellular physiology'),
(313615, 'HP:0200024', 'Premature chromatid separation', 'XPO:0135716', 'increased cell population proliferation in portion of organism substance', 0.425, 5.835653092541957, 1.5748500132807353, 'HP:0011017', 'Abnormal cellular physiology'),
(313616, 'HP:0200024', 'Premature chromatid separation', 'XPO:0131707', 'abnormal cilium assembly', 0.5757575757575758, 8.76910634777607, 2.246971164113131, 'UPHENO:0049700', 'abnormal organelle organization'),
(313617, 'HP:0200024', 'Premature chromatid separation', 'XPO:0100218', 'abnormal epithelial cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(313618, 'HP:0200024', 'Premature chromatid separation', 'XPO:0131706', 'abnormal ciliary basal body organization', 0.6129032258064516, 8.76910634777607, 2.3183212823057517, 'UPHENO:0049700', 'abnormal organelle organization'),
(313619, 'HP:0200024', 'Premature chromatid separation', 'XPO:0101468', 'abnormal stage I oocyte', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(313620, 'HP:0200024', 'Premature chromatid separation', 'XPO:0100026', 'abnormal germ cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(313621, 'HP:0200024', 'Premature chromatid separation', 'XPO:0101461', 'abnormal sperm entry point', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(313622, 'HP:0200024', 'Premature chromatid separation', 'XPO:0101389', 'abnormal wedge region', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(313623, 'HP:0200024', 'Premature chromatid separation', 'XPO:0100307', 'abnormal blastomere', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(313624, 'HP:0200024', 'Premature chromatid separation', 'XPO:0100989', 'abnormal right blastomere', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(313625, 'HP:0200024', 'Premature chromatid separation', 'XPO:0100907', 'abnormal cytoplasm', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(313626, 'HP:0200024', 'Premature chromatid separation', 'XPO:0100784', 'abnormal left blastomere', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(313627, 'HP:0200024', 'Premature chromatid separation', 'XPO:0101220', 'abnormal centriole', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(313628, 'HP:0200024', 'Premature chromatid separation', 'XPO:0135636', 'increased cell population proliferation in anatomical region', 0.40476190476190477, 5.835653092541957, 1.5368962428436679, 'HP:0011017', 'Abnormal cellular physiology'),
(313629, 'HP:0200024', 'Premature chromatid separation', 'XPO:0103642', 'increased cell population proliferation', 0.4857142857142857, 5.835653092541957, 1.6835854815008293, 'HP:0011017', 'Abnormal cellular physiology'),
(313630, 'HP:0200024', 'Premature chromatid separation', 'XPO:0100674', 'abnormal secondary oogonium', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(313631, 'HP:0200024', 'Premature chromatid separation', 'XPO:0100503', 'abnormal blastomere D2', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(313632, 'HP:0200024', 'Premature chromatid separation', 'XPO:0100429', 'abnormal spermatid', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(313633, 'HP:0200024', 'Premature chromatid separation', 'XPO:0136321', 'increased cell population proliferation in multicellular anatomical structure', 0.40476190476190477, 5.835653092541957, 1.5368962428436679, 'HP:0011017', 'Abnormal cellular physiology'),
(313634, 'HP:0200024', 'Premature chromatid separation', 'XPO:0100715', 'abnormal ciliated cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(313635, 'HP:0200024', 'Premature chromatid separation', 'XPO:0101409', 'abnormal perivitelline space', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(313636, 'HP:0200024', 'Premature chromatid separation', 'XPO:0100754', 'abnormal electrically active cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(313637, 'HP:0200024', 'Premature chromatid separation', 'XPO:0100289', 'abnormal chondroblast', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(313638, 'HP:0200024', 'Premature chromatid separation', 'XPO:0100437', 'abnormal proepicardium', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(313639, 'HP:0200024', 'Premature chromatid separation', 'XPO:0101004', 'abnormal acid secreting cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(313640, 'HP:0200024', 'Premature chromatid separation', 'XPO:0138579', 'decreased cell population proliferation in whole organism', 0.4146341463414634, 5.835653092541957, 1.5555259684013814, 'HP:0011017', 'Abnormal cellular physiology'),
(313641, 'HP:0200024', 'Premature chromatid separation', 'XPO:0138837', 'decreased cell population proliferation in process', 0.40476190476190477, 5.835653092541957, 1.5368962428436679, 'HP:0011017', 'Abnormal cellular physiology'),
(313642, 'HP:0200024', 'Premature chromatid separation', 'XPO:0101072', 'abnormal mitochondrial cloud', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(313643, 'HP:0200024', 'Premature chromatid separation', 'XPO:0100721', 'abnormal centromere', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(313644, 'HP:0200024', 'Premature chromatid separation', 'XPO:0100337', 'abnormal zygote', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(313645, 'HP:0200024', 'Premature chromatid separation', 'XPO:0141776', 'abnormal metabolic process', 0.42857142857142855, 4.758907843651163, 1.4281218200816608, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(313646, 'HP:0200024', 'Premature chromatid separation', 'XPO:0135720', 'increased cell population proliferation in extraembryonic structure', 0.40476190476190477, 5.835653092541957, 1.5368962428436679, 'HP:0011017', 'Abnormal cellular physiology'),
(313647, 'HP:0200024', 'Premature chromatid separation', 'XPO:0101228', 'abnormal mesenchymal stem cell', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(313648, 'HP:0200024', 'Premature chromatid separation', 'XPO:0141421', 'decreased cell population proliferation in tadpole', 0.40476190476190477, 5.835653092541957, 1.5368962428436679, 'HP:0011017', 'Abnormal cellular physiology'),
(313649, 'HP:0200024', 'Premature chromatid separation', 'XPO:0101463', 'abnormal right-ventral blastomere', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(313650, 'HP:0200024', 'Premature chromatid separation', 'XPO:0101378', 'abnormal blastomere D1', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(313651, 'HP:0200024', 'Premature chromatid separation', 'XPO:0138577', 'decreased cell population proliferation in anatomical group', 0.40476190476190477, 5.835653092541957, 1.5368962428436679, 'HP:0011017', 'Abnormal cellular physiology'),
(313652, 'HP:0200024', 'Premature chromatid separation', 'XPO:0131685', 'abnormal cortical actin cytoskeleton', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(313653, 'HP:0200024', 'Premature chromatid separation', 'XPO:0141877', 'abnormal 2-deoxyribose 1-phosphate metabolic process', 0.40625, 4.758907843651163, 1.3904338572845834, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(313654, 'HP:0200024', 'Premature chromatid separation', 'XPO:0135735', 'increased cell population proliferation in process', 0.40476190476190477, 5.835653092541957, 1.5368962428436679, 'HP:0011017', 'Abnormal cellular physiology'),
(313655, 'HP:0200024', 'Premature chromatid separation', 'XPO:0101513', 'abnormal basal body', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(313656, 'HP:0200024', 'Premature chromatid separation', 'XPO:0101237', 'abnormal mucus secreting cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(313657, 'HP:0200024', 'Premature chromatid separation', 'XPO:0100308', 'abnormal early embryonic cell', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(313658, 'HP:0200024', 'Premature chromatid separation', 'XPO:0101472', 'abnormal zygote cortex', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(313659, 'HP:0200024', 'Premature chromatid separation', 'XPO:0138262', 'decreased cell population proliferation in embryo', 0.40476190476190477, 5.835653092541957, 1.5368962428436679, 'HP:0011017', 'Abnormal cellular physiology'),
(313660, 'HP:0200024', 'Premature chromatid separation', 'XPO:0100025', 'abnormal oocyte', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(313661, 'HP:0200024', 'Premature chromatid separation', 'XPO:0135615', 'increased cell population proliferation in acellular anatomical structure', 0.40476190476190477, 5.835653092541957, 1.5368962428436679, 'HP:0011017', 'Abnormal cellular physiology'),
(313662, 'HP:0200024', 'Premature chromatid separation', 'XPO:0101240', 'abnormal ciliated non-epidermal cell', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(313663, 'HP:0200024', 'Premature chromatid separation', 'XPO:0101061', 'abnormal plasma membrane', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(313664, 'HP:0200024', 'Premature chromatid separation', 'XPO:0100976', 'abnormal multiciliated cell', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(313665, 'HP:0200024', 'Premature chromatid separation', 'XPO:0100172', 'abnormal stem cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(313666, 'HP:0200024', 'Premature chromatid separation', 'XPO:0131675', 'abnormal spindle microtubule', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(313667, 'HP:0200024', 'Premature chromatid separation', 'XPO:0100626', 'abnormal primordial germ cell', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(313668, 'HP:0200024', 'Premature chromatid separation', 'XPO:0100638', 'abnormal polar body', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(313669, 'HP:0200024', 'Premature chromatid separation', 'XPO:0100791', 'abnormal multiciliated cell precursor', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(313670, 'HP:0200024', 'Premature chromatid separation', 'XPO:0135479', 'increased cell population proliferation in male organism', 0.40476190476190477, 5.835653092541957, 1.5368962428436679, 'HP:0011017', 'Abnormal cellular physiology'),
(313671, 'HP:0200024', 'Premature chromatid separation', 'XPO:0141911', 'abnormal ribose phosphate metabolic process', 0.40625, 4.758907843651163, 1.3904338572845834, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(313672, 'HP:0200024', 'Premature chromatid separation', 'XPO:0101435', 'abnormal paracrine cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(313673, 'HP:0200024', 'Premature chromatid separation', 'XPO:0100574', 'abnormal gastrula cell', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(313674, 'HP:0200024', 'Premature chromatid separation', 'XPO:0138822', 'decreased cell population proliferation in extraembryonic structure', 0.40476190476190477, 5.835653092541957, 1.5368962428436679, 'HP:0011017', 'Abnormal cellular physiology'),
(313675, 'HP:0200024', 'Premature chromatid separation', 'XPO:0100547', 'abnormal blastomere V2', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(313676, 'HP:0200024', 'Premature chromatid separation', 'XPO:0138838', 'decreased cell population proliferation in cell condensation', 0.40476190476190477, 5.835653092541957, 1.5368962428436679, 'HP:0011017', 'Abnormal cellular physiology'),
(313677, 'HP:0200024', 'Premature chromatid separation', 'XPO:0101535', 'abnormal absorptive cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(313678, 'HP:0200024', 'Premature chromatid separation', 'XPO:0101575', 'abnormal vitelline membrane', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(313679, 'HP:0200024', 'Premature chromatid separation', 'XPO:0100392', 'abnormal cilium', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(313680, 'HP:0200024', 'Premature chromatid separation', 'XPO:0101311', 'abnormal bottle cell', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(313681, 'HP:0200024', 'Premature chromatid separation', 'XPO:0101136', 'abnormal ooplasm', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(313682, 'HP:0200024', 'Premature chromatid separation', 'XPO:0101480', 'abnormal stage V oocyte', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(313683, 'HP:0200024', 'Premature chromatid separation', 'XPO:0100176', 'abnormal stage VI oocyte', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(313684, 'HP:0200024', 'Premature chromatid separation', 'XPO:0138576', 'decreased cell population proliferation in anatomical structure', 0.425, 5.835653092541957, 1.5748500132807353, 'HP:0011017', 'Abnormal cellular physiology'),
(313685, 'HP:0200024', 'Premature chromatid separation', 'XPO:0101326', 'abnormal cementoblast', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(313686, 'HP:0200024', 'Premature chromatid separation', 'XPO:0131708', 'abnormal cilium disassembly', 0.6129032258064516, 8.76910634777607, 2.3183212823057517, 'UPHENO:0049700', 'abnormal organelle organization'),
(313687, 'HP:0200024', 'Premature chromatid separation', 'XPO:0101448', 'abnormal myelin accumulating cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(313688, 'HP:0200024', 'Premature chromatid separation', 'XPO:0107312', 'abnormal filopodium', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(313689, 'HP:0200024', 'Premature chromatid separation', 'XPO:0100477', 'abnormal pericyte', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(313690, 'HP:0200024', 'Premature chromatid separation', 'XPO:0141860', 'abnormal malate-aspartate shuttle', 0.43333333333333335, 4.758907843651163, 1.4360339128709683, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(313691, 'HP:0200024', 'Premature chromatid separation', 'XPO:0101297', 'abnormal barrier cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(313692, 'HP:0200024', 'Premature chromatid separation', 'XPO:0101373', 'abnormal oxygen accumulating cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(313693, 'HP:0200024', 'Premature chromatid separation', 'XPO:0101264', 'abnormal mitotic spindle', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(313694, 'HP:0200024', 'Premature chromatid separation', 'XPO:0141790', 'abnormal cellular metabolic process', 0.43333333333333335, 4.758907843651163, 1.4360339128709683, 'HP:0001939', 'Abnormality of metabolism/homeostasis'),
(313695, 'HP:0200024', 'Premature chromatid separation', 'XPO:0131677', 'abnormal actin filament', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(313696, 'HP:0200024', 'Premature chromatid separation', 'XPO:0138738', 'decreased cell population proliferation in anatomical region', 0.40476190476190477, 5.835653092541957, 1.5368962428436679, 'HP:0011017', 'Abnormal cellular physiology'),
(313697, 'HP:0200024', 'Premature chromatid separation', 'XPO:0100653', 'abnormal myoblast', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(313698, 'HP:0200024', 'Premature chromatid separation', 'XPO:0100551', 'abnormal oocyte cortex', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(313699, 'HP:0200024', 'Premature chromatid separation', 'XPO:0101302', 'abnormal subcortical cytoplasm', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(313700, 'HP:0200024', 'Premature chromatid separation', 'XPO:0136191', 'increased cell population proliferation in organ part', 0.4146341463414634, 5.835653092541957, 1.5555259684013814, 'HP:0011017', 'Abnormal cellular physiology'),
(313701, 'HP:0200024', 'Premature chromatid separation', 'XPO:0101241', 'abnormal nucleate erythrocyte', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(313702, 'HP:0200024', 'Premature chromatid separation', 'XPO:0100004', 'abnormal cell', 0.4642857142857143, 3.6715585125471644, 1.305623286610558, 'UPHENO:0086172', 'abnormal cell'),
(313703, 'HP:0200024', 'Premature chromatid separation', 'XPO:0100724', 'abnormal kinetochore', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(313704, 'HP:0200024', 'Premature chromatid separation', 'XPO:0138820', 'decreased cell population proliferation in anatomical line', 0.425, 5.835653092541957, 1.5748500132807353, 'HP:0011017', 'Abnormal cellular physiology'),
(313705, 'HP:0200024', 'Premature chromatid separation', 'XPO:0138818', 'decreased cell population proliferation in portion of organism substance', 0.425, 5.835653092541957, 1.5748500132807353, 'HP:0011017', 'Abnormal cellular physiology'),
(313706, 'HP:0200024', 'Premature chromatid separation', 'XPO:0101132', 'abnormal apoptotic cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(313707, 'HP:0200024', 'Premature chromatid separation', 'XPO:0100802', 'abnormal exocrine cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(313708, 'HP:0200024', 'Premature chromatid separation', 'XPO:0135477', 'increased cell population proliferation in whole organism', 0.4146341463414634, 5.835653092541957, 1.5555259684013814, 'HP:0011017', 'Abnormal cellular physiology'),
(313709, 'HP:0200024', 'Premature chromatid separation', 'XPO:0138580', 'decreased cell population proliferation in female organism', 0.40476190476190477, 5.835653092541957, 1.5368962428436679, 'HP:0011017', 'Abnormal cellular physiology'),
(313710, 'HP:0200024', 'Premature chromatid separation', 'XPO:0101405', 'abnormal ring structure', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(313711, 'HP:0200024', 'Premature chromatid separation', 'XPO:0131687', 'abnormal astral microtubule', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(313712, 'HP:0200024', 'Premature chromatid separation', 'XPO:0100902', 'abnormal spermatocyte', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(313713, 'HP:0200024', 'Premature chromatid separation', 'XPO:0100704', 'abnormal Merkel cell', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(313714, 'HP:0200024', 'Premature chromatid separation', 'XPO:0101113', 'abnormal stage IV oocyte', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(313715, 'HP:0200024', 'Premature chromatid separation', 'XPO:0139293', 'decreased cell population proliferation in organ part', 0.4146341463414634, 5.835653092541957, 1.5555259684013814, 'HP:0011017', 'Abnormal cellular physiology'),
(313716, 'HP:0200024', 'Premature chromatid separation', 'XPO:0131735', 'abnormal spindle assembly', 0.625, 10.281312506061912, 2.534920179470883, 'HP:0002916', 'Abnormality of chromosome segregation'),
(313717, 'HP:0200024', 'Premature chromatid separation', 'XPO:0131666', 'abnormal adherens junction', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(313718, 'HP:0200024', 'Premature chromatid separation', 'XPO:0100917', 'abnormal stage III oocyte', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(313719, 'HP:0200024', 'Premature chromatid separation', 'XPO:0101498', 'abnormal stage II oocyte', 0.41935483870967744, 3.6715585125471644, 1.240840774572773, 'UPHENO:0086172', 'abnormal cell'),
(313720, 'HP:0200024', 'Premature chromatid separation', 'XPO:0100108', 'abnormal cell part', 0.4482758620689655, 3.6715585125471644, 1.2829150624062098, 'UPHENO:0086172', 'abnormal cell'),
(313721, 'HP:0200024', 'Premature chromatid separation', 'XPO:0107284', 'abnormal migrating myoblast', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(313722, 'HP:0200024', 'Premature chromatid separation', 'XPO:0100888', 'abnormal microtubule', 0.43333333333333335, 3.6715585125471644, 1.2613519289914445, 'UPHENO:0086172', 'abnormal cell'),
(313723, 'HP:0200024', 'Premature chromatid separation', 'XPO:0135475', 'increased cell population proliferation in anatomical group', 0.40476190476190477, 5.835653092541957, 1.5368962428436679, 'HP:0011017', 'Abnormal cellular physiology'),
(313724, 'HP:0200024', 'Premature chromatid separation', 'XPO:0100862', 'abnormal blastomere V1', 0.40625, 3.6715585125471644, 1.221298753672616, 'UPHENO:0086172', 'abnormal cell'),
(313725, 'HP:0010347', 'Aplasia/Hypoplasia of the phalanges of the 2nd toe', 'XPO:0141529', 'absent hindlimb digit 3 in the regenerating hindlimb', 0.41228070175438597, 10.299160507394836, 2.0606176553329347, 'HP:0006494', 'Aplasia/Hypoplasia involving bones of the feet'),
(313726, 'HP:0010347', 'Aplasia/Hypoplasia of the phalanges of the 2nd toe', 'XPO:0103571', 'decreased length of hindlimb digit', 0.40869565217391307, 10.299160507394836, 2.0516388864548123, 'HP:0006494', 'Aplasia/Hypoplasia involving bones of the feet'),
(313727, 'HP:0010347', 'Aplasia/Hypoplasia of the phalanges of the 2nd toe', 'XPO:0103589', 'abnormally decreased number of hindlimb digit', 0.415929203539823, 10.299160507394836, 2.0697153492617124, 'HP:0006494', 'Aplasia/Hypoplasia involving bones of the feet'),
(313728, 'HP:0010347', 'Aplasia/Hypoplasia of the phalanges of the 2nd toe', 'XPO:0141524', 'absent hindlimb digit 1 in the regenerating hindlimb', 0.41228070175438597, 10.299160507394836, 2.0606176553329347, 'HP:0006494', 'Aplasia/Hypoplasia involving bones of the feet'),
(313729, 'HP:0010347', 'Aplasia/Hypoplasia of the phalanges of the 2nd toe', 'XPO:0103290', 'absent hindlimb digit 2', 0.4392523364485981, 10.299160507394836, 2.1269532943467073, 'HP:0006494', 'Aplasia/Hypoplasia involving bones of the feet'),
(313730, 'HP:0010347', 'Aplasia/Hypoplasia of the phalanges of the 2nd toe', 'XPO:0103291', 'absent hindlimb digit 3', 0.4392523364485981, 10.299160507394836, 2.1269532943467073, 'HP:0006494', 'Aplasia/Hypoplasia involving bones of the feet'),
(313731, 'HP:0010347', 'Aplasia/Hypoplasia of the phalanges of the 2nd toe', 'XPO:0103289', 'absent hindlimb digit', 0.4519230769230769, 10.299160507394836, 2.1574124098619887, 'HP:0006494', 'Aplasia/Hypoplasia involving bones of the feet'),
(313732, 'HP:0010347', 'Aplasia/Hypoplasia of the phalanges of the 2nd toe', 'XPO:0103292', 'absent hindlimb digit 4', 0.4392523364485981, 10.299160507394836, 2.1269532943467073, 'HP:0006494', 'Aplasia/Hypoplasia involving bones of the feet'),
(313733, 'HP:0010347', 'Aplasia/Hypoplasia of the phalanges of the 2nd toe', 'XPO:0141528', 'absent hindlimb digit 2 in the regenerating hindlimb', 0.41228070175438597, 10.299160507394836, 2.0606176553329347, 'HP:0006494', 'Aplasia/Hypoplasia involving bones of the feet'),
(313734, 'HP:0010347', 'Aplasia/Hypoplasia of the phalanges of the 2nd toe', 'XPO:0102566', 'abnormal claw primordium morphology', 0.40425531914893614, 7.639349617137506, 1.7573410931194393, 'UPHENO:0088132', 'abnormal pedal digit morphology'),
(313735, 'HP:0010347', 'Aplasia/Hypoplasia of the phalanges of the 2nd toe', 'XPO:0103293', 'absent hindlimb digit 5', 0.4392523364485981, 10.299160507394836, 2.1269532943467073, 'HP:0006494', 'Aplasia/Hypoplasia involving bones of the feet'),
(313736, 'HP:0010347', 'Aplasia/Hypoplasia of the phalanges of the 2nd toe', 'XPO:0103908', 'absent hindlimb digit 1', 0.4392523364485981, 10.299160507394836, 2.1269532943467073, 'HP:0006494', 'Aplasia/Hypoplasia involving bones of the feet'),
(313737, 'HP:0033882', 'Arcuate vein intima/medial amyloidosis', 'XPO:0101717', 'abnormal mesonephric sinus morphology', 0.5476190476190477, 7.603795021646889, 2.040583982110201, 'HP:0012210', 'Abnormal renal morphology'),
(313738, 'HP:0033882', 'Arcuate vein intima/medial amyloidosis', 'XPO:0107300', 'abnormal embryonic kidney', 0.4634146341463415, 6.880013295263146, 1.7855808142300187, 'HP:0000077', 'Abnormality of the kidney'),
(313739, 'HP:0033882', 'Arcuate vein intima/medial amyloidosis', 'XPO:0107301', 'abnormal adult kidney', 0.4634146341463415, 6.880013295263146, 1.7855808142300187, 'HP:0000077', 'Abnormality of the kidney'),
(313740, 'HP:0033882', 'Arcuate vein intima/medial amyloidosis', 'XPO:0100271', 'abnormal mesonephric nephron', 0.40425531914893614, 6.880013295263146, 1.6677175931270638, 'HP:0000077', 'Abnormality of the kidney'),
(313741, 'HP:0033882', 'Arcuate vein intima/medial amyloidosis', 'XPO:0130678', 'increased size of the mesonephric sinus', 0.48936170212765956, 7.603795021646889, 1.9289909472112474, 'HP:0012210', 'Abnormal renal morphology'),
(313742, 'HP:0033882', 'Arcuate vein intima/medial amyloidosis', 'XPO:0126072', 'absent mesonephric sinus', 0.40425531914893614, 6.880013295263146, 1.6677175931270638, 'HP:0000077', 'Abnormality of the kidney'),
(313743, 'HP:0033882', 'Arcuate vein intima/medial amyloidosis', 'XPO:0103182', 'abnormal pronephric sinus morphology', 0.40350877192982454, 7.603795021646889, 1.7516272409365097, 'HP:0012210', 'Abnormal renal morphology'),
(313744, 'HP:0033882', 'Arcuate vein intima/medial amyloidosis', 'XPO:0107388', 'abnormal adult kidney morphology', 0.45098039215686275, 7.603795021646889, 1.8517997895946297, 'HP:0012210', 'Abnormal renal morphology'),
(313745, 'HP:0033882', 'Arcuate vein intima/medial amyloidosis', 'XPO:0126710', 'abnormally localised kidney', 0.4339622641509434, 7.603795021646889, 1.816524181984252, 'HP:0012210', 'Abnormal renal morphology'),
(313746, 'HP:0033882', 'Arcuate vein intima/medial amyloidosis', 'XPO:0100778', 'abnormal mesonephric kidney', 0.41304347826086957, 6.880013295263146, 1.685747496500148, 'HP:0000077', 'Abnormality of the kidney'),
(313747, 'HP:0033882', 'Arcuate vein intima/medial amyloidosis', 'XPO:0102198', 'abnormal kidney morphology', 0.46938775510204084, 7.603795021646889, 1.8892136659115366, 'HP:0012210', 'Abnormal renal morphology'),
(313748, 'HP:0033882', 'Arcuate vein intima/medial amyloidosis', 'XPO:0100566', 'abnormal kidney', 0.475, 6.880013295263146, 1.8077627928602786, 'HP:0000077', 'Abnormality of the kidney'),
(313749, 'HP:0033882', 'Arcuate vein intima/medial amyloidosis', 'XPO:0141643', 'neoplastic kidney', 0.4423076923076923, 7.603795021646889, 1.833907584586899, 'HP:0012210', 'Abnormal renal morphology'),
(313750, 'HP:0033882', 'Arcuate vein intima/medial amyloidosis', 'XPO:0101701', 'abnormal urinary system morphology', 0.40476190476190477, 7.340144605965611, 1.7236620643091445, 'UPHENO:0087427', 'abnormal renal system morphology'),
(313751, 'HP:0033882', 'Arcuate vein intima/medial amyloidosis', 'XPO:0100147', 'abnormal mesonephric mesenchyme', 0.48717948717948717, 6.880013295263146, 1.83079254667872, 'HP:0000077', 'Abnormality of the kidney'),
(313752, 'HP:0033882', 'Arcuate vein intima/medial amyloidosis', 'XPO:0107387', 'abnormal embryonic kidney morphology', 0.45098039215686275, 7.603795021646889, 1.8517997895946297, 'HP:0012210', 'Abnormal renal morphology'),
(313753, 'HP:0033882', 'Arcuate vein intima/medial amyloidosis', 'XPO:0101779', 'abnormal mesonephric mesenchyme morphology', 0.46, 7.603795021646889, 1.870226111986882, 'HP:0012210', 'Abnormal renal morphology'),
(313754, 'HP:0033882', 'Arcuate vein intima/medial amyloidosis', 'XPO:0100567', 'abnormal mesonephric collecting duct', 0.42592592592592593, 7.603795021646889, 1.7996259153351557, 'HP:0012210', 'Abnormal renal morphology'),
(313755, 'HP:0033882', 'Arcuate vein intima/medial amyloidosis', 'XPO:0126656', 'abnormally localised embryonic kidney', 0.41818181818181815, 7.603795021646889, 1.7831906312097294, 'HP:0012210', 'Abnormal renal morphology'),
(313756, 'HP:0033882', 'Arcuate vein intima/medial amyloidosis', 'XPO:0100761', 'abnormal ureter', 0.425, 6.828345551150745, 1.703539509151187, 'HP:0010935', 'Abnormality of the upper urinary tract'),
(313757, 'HP:0033882', 'Arcuate vein intima/medial amyloidosis', 'XPO:0127733', 'abnormally localised mesonephric sinus', 0.4418604651162791, 6.880013295263146, 1.7435612620872136, 'HP:0000077', 'Abnormality of the kidney'),
(313758, 'HP:0033882', 'Arcuate vein intima/medial amyloidosis', 'XPO:0100069', 'abnormal urinary system', 0.42857142857142855, 6.355235291121788, 1.6503551943819923, 'HP:0000079', 'Abnormality of the urinary system'),
(313759, 'HP:0033882', 'Arcuate vein intima/medial amyloidosis', 'XPO:0141613', 'metaplastic kidney', 0.4318181818181818, 6.880013295263146, 1.7236341932224046, 'HP:0000077', 'Abnormality of the kidney'),
(313760, 'HP:0033882', 'Arcuate vein intima/medial amyloidosis', 'XPO:0126885', 'abnormally localised adult kidney', 0.41818181818181815, 7.603795021646889, 1.7831906312097294, 'HP:0012210', 'Abnormal renal morphology'),
(313761, 'HP:0033882', 'Arcuate vein intima/medial amyloidosis', 'XPO:0140552', 'abnormally necrotic kidney', 0.40350877192982454, 7.603795021646889, 1.7516272409365097, 'HP:0012210', 'Abnormal renal morphology'),
(313762, 'HP:0033882', 'Arcuate vein intima/medial amyloidosis', 'XPO:0100085', 'abnormal mesonephric sinus', 0.5277777777777778, 6.880013295263146, 1.9055492982485522, 'HP:0000077', 'Abnormality of the kidney'),
(313763, 'HP:0033882', 'Arcuate vein intima/medial amyloidosis', 'XPO:0140815', 'abnormally necrotic mesonephric mesenchyme', 0.4107142857142857, 7.603795021646889, 1.7671975670630444, 'HP:0012210', 'Abnormal renal morphology'),
(313764, 'HP:0033882', 'Arcuate vein intima/medial amyloidosis', 'XPO:0129202', 'decreased size of the mesonephric sinus', 0.48936170212765956, 7.603795021646889, 1.9289909472112474, 'HP:0012210', 'Abnormal renal morphology'),
(313765, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0141294', 'abnormal sarcomere morphology', 0.4146341463414634, 6.895202660022325, 1.6908537691916898, 'HP:0011805', 'Abnormal skeletal muscle morphology'),
(313766, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0101513', 'abnormal basal body', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(313767, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0141776', 'abnormal metabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(313768, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0141718', 'abnormal posterior notochord', 0.42857142857142855, 3.9037819259951223, 1.293464107292913, 'HP:0033127', 'Abnormality of the musculoskeletal system'),
(313769, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0107312', 'abnormal filopodium', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(313770, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0100372', 'abnormal hematological system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(313771, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0100108', 'abnormal cell part', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(313772, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0101153', 'abnormal musculature of face', 0.40476190476190477, 6.895202660022325, 1.6706032929423995, 'HP:0011805', 'Abnormal skeletal muscle morphology'),
(313773, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0101435', 'abnormal paracrine cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(313774, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0100422', 'abnormal notochord', 0.4444444444444444, 3.9037819259951223, 1.3171993734173904, 'HP:0033127', 'Abnormality of the musculoskeletal system'),
(313775, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0101467', 'abnormal alkali secreting cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(313776, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0100852', 'abnormal interdigital region', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(313777, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0100501', 'abnormal urogenital system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(313778, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0100644', 'abnormal smooth muscle myocyte', 0.4117647058823529, 5.968280811662945, 1.5676502776568768, 'UPHENO:0002816', 'abnormal musculature'),
(313779, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0100902', 'abnormal spermatocyte', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(313780, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0100728', 'abnormal cell condensation', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(313781, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0115509', 'abnormally semi-viable whole organism', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(313782, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0107259', 'abnormal animal-vegetal axis', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(313783, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0100010', 'abnormal multicellular anatomical structure', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(313784, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0101480', 'abnormal stage V oocyte', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(313785, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0107261', 'abnormal dorsal-ventral axis', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(313786, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0100392', 'abnormal cilium', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(313787, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0100956', 'abnormal centrosome', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(313788, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0101264', 'abnormal mitotic spindle', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(313789, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0100674', 'abnormal secondary oogonium', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(313790, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0100894', 'abnormal nucleus', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(313791, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0100640', 'abnormal notochordal sheath', 0.42857142857142855, 3.9037819259951223, 1.293464107292913, 'HP:0033127', 'Abnormality of the musculoskeletal system'),
(313792, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0100025', 'abnormal oocyte', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(313793, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0101174', 'abnormal articular system', 0.42857142857142855, 3.9037819259951223, 1.293464107292913, 'HP:0033127', 'Abnormality of the musculoskeletal system'),
(313794, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:00000000', 'Xenopus phenotype', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(313795, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0101004', 'abnormal acid secreting cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(313796, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0100258', 'abnormal organ part', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(313797, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0100032', 'abnormal nervous system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(313798, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0101297', 'abnormal barrier cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(313799, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0107253', 'abnormal enteric nervous system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(313800, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0101221', 'abnormal larval immune system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(313801, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0100839', 'abnormal skeletal myocyte', 0.4117647058823529, 5.968280811662945, 1.5676502776568768, 'UPHENO:0002816', 'abnormal musculature'),
(313802, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0100899', 'abnormal secondary spermatogonium', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(313803, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0101228', 'abnormal mesenchymal stem cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(313804, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0100084', 'abnormal anatomical group', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(313805, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0100225', 'abnormal endocrine system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(313806, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0100638', 'abnormal polar body', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(313807, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0101071', 'abnormal endoplasmic reticulum', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(313808, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0101237', 'abnormal mucus secreting cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(313809, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0100596', 'abnormal myocyte', 0.4375, 5.968280811662945, 1.6158969197020392, 'UPHENO:0002816', 'abnormal musculature'),
(313810, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0101240', 'abnormal ciliated non-epidermal cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(313811, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0107258', 'abnormal anatomical axis', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(313812, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0107285', 'abnormal flexural organ', 0.42857142857142855, 3.9037819259951223, 1.293464107292913, 'HP:0033127', 'Abnormality of the musculoskeletal system'),
(313813, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0100274', 'abnormal sensory system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(313814, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0100746', 'abnormal smooth muscle', 0.4827586206896552, 5.968280811662945, 1.6974212831607063, 'UPHENO:0002816', 'abnormal musculature'),
(313815, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0100585', 'abnormal elastica externa', 0.46153846153846156, 3.9037819259951223, 1.3422911399191462, 'HP:0033127', 'Abnormality of the musculoskeletal system'),
(313816, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0100239', 'abnormal acellular anatomical structure', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(313817, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0141714', 'abnormal anterior notochord', 0.42857142857142855, 3.9037819259951223, 1.293464107292913, 'HP:0033127', 'Abnormality of the musculoskeletal system'),
(313818, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0101409', 'abnormal perivitelline space', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(313819, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0103113', 'abnormal skeletal muscle satellite cell morphology', 0.4146341463414634, 6.895202660022325, 1.6908537691916898, 'HP:0011805', 'Abnormal skeletal muscle morphology'),
(313820, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0107284', 'abnormal migrating myoblast', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(313821, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0100202', 'abnormal embryo', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(313822, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0101061', 'abnormal plasma membrane', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(313823, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0100754', 'abnormal electrically active cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(313824, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0131685', 'abnormal cortical actin cytoskeleton', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(313825, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0100626', 'abnormal primordial germ cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(313826, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0102228', 'abnormal myocyte morphology', 0.425, 6.895202660022325, 1.7118589692230748, 'HP:0011805', 'Abnormal skeletal muscle morphology'),
(313827, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0100533', 'abnormal melanoblast', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(313828, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0100721', 'abnormal centromere', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(313829, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0141284', 'abnormal myofibril morphology', 0.425, 6.895202660022325, 1.7118589692230748, 'HP:0011805', 'Abnormal skeletal muscle morphology'),
(313830, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0101448', 'abnormal myelin accumulating cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(313831, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0100275', 'abnormal skeletal muscle', 0.4827586206896552, 5.968280811662945, 1.6974212831607063, 'UPHENO:0002816', 'abnormal musculature'),
(313832, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0100423', 'abnormal process', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(313833, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0141315', 'abnormal anatomical region', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(313834, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0101569', 'abnormal activin-induced ectoderm', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(313835, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0100429', 'abnormal spermatid', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(313836, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0101366', 'abnormal morula cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(313837, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0101976', 'abnormal portion of organism substance morphology', 0.4166666666666667, 2.485033483301678, 1.0175611126818702, 'UPHENO:0076692', 'abnormal anatomical entity morphology'),
(313838, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0100006', 'abnormal anatomical structure', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(313839, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0100416', 'abnormal ligament', 0.42857142857142855, 3.9037819259951223, 1.293464107292913, 'HP:0033127', 'Abnormality of the musculoskeletal system'),
(313840, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0100337', 'abnormal zygote', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(313841, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0100768', 'abnormal pectoral girdle', 0.40476190476190477, 6.895202660022325, 1.6706032929423995, 'HP:0011805', 'Abnormal skeletal muscle morphology'),
(313842, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0100724', 'abnormal kinetochore', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(313843, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0100573', 'abnormal extraembryonic structure', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(313844, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0100232', 'abnormal lymphatic system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(313845, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0101333', 'abnormal barrier epithelial cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(313846, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0100581', 'abnormal immune system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(313847, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0100377', 'abnormal connective tissue', 0.46153846153846156, 3.9037819259951223, 1.3422911399191462, 'HP:0033127', 'Abnormality of the musculoskeletal system'),
(313848, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0100176', 'abnormal stage VI oocyte', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(313849, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0101535', 'abnormal absorptive cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(313850, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0101110', 'abnormal cell-free extract', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(313851, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0101547', 'abnormal lampbrush chromosome', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(313852, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0101241', 'abnormal nucleate erythrocyte', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(313853, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0101466', 'abnormal secondary myofiber', 0.4375, 5.968280811662945, 1.6158969197020392, 'UPHENO:0002816', 'abnormal musculature'),
(313854, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0100031', 'abnormal central nervous system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(313855, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0101732', 'abnormal muscle morphology', 0.4857142857142857, 6.895202660022325, 1.8300542163739266, 'HP:0011805', 'Abnormal skeletal muscle morphology'),
(313856, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0107270', 'abnormal proximal-distal axis', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(313857, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0100285', 'abnormal progenitor cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(313858, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0100688', 'abnormal adipose tissue', 0.4444444444444444, 3.9037819259951223, 1.3171993734173904, 'HP:0033127', 'Abnormality of the musculoskeletal system'),
(313859, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0100437', 'abnormal proepicardium', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(313860, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0115508', 'abnormally peramorphic growth of whole organism', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(313861, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0100791', 'abnormal multiciliated cell precursor', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(313862, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0101157', 'abnormal female organism', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(313863, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0131677', 'abnormal actin filament', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(313864, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0100691', 'abnormal keratin accumulating cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(313865, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0100546', 'abnormal whole organism', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(313866, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0100081', 'abnormal anatomical entity in vitro', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(313867, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0100172', 'abnormal stem cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(313868, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0103736', 'increased size of the muscle', 0.40476190476190477, 6.895202660022325, 1.6706032929423995, 'HP:0011805', 'Abnormal skeletal muscle morphology'),
(313869, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0100004', 'abnormal cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(313870, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0100907', 'abnormal cytoplasm', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(313871, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0142057', 'abnormal desmosome', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(313872, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0141307', 'abnormal M band morphology', 0.40476190476190477, 6.895202660022325, 1.6706032929423995, 'HP:0011805', 'Abnormal skeletal muscle morphology'),
(313873, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0101113', 'abnormal stage IV oocyte', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(313874, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0139779', 'abnormally necrotic muscle', 0.425, 6.895202660022325, 1.7118589692230748, 'HP:0011805', 'Abnormal skeletal muscle morphology'),
(313875, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0100715', 'abnormal ciliated cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(313876, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0100477', 'abnormal pericyte', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(313877, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0100308', 'abnormal early embryonic cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(313878, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0115512', 'abnormally semi-erect whole organism', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(313879, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0101141', 'abnormal Keller explant', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(313880, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0100317', 'abnormal respiratory system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(313881, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0100307', 'abnormal blastomere', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(313882, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0100802', 'abnormal exocrine cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(313883, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0100976', 'abnormal multiciliated cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(313884, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0101326', 'abnormal cementoblast', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(313885, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0100515', 'abnormal somatic stem cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(313886, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0100100', 'abnormal muscle', 0.5, 5.968280811662945, 1.7274664702481124, 'UPHENO:0002816', 'abnormal musculature'),
(313887, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0131675', 'abnormal spindle microtubule', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(313888, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0101132', 'abnormal apoptotic cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(313889, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0101373', 'abnormal oxygen accumulating cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(313890, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0101096', 'abnormal tendon', 0.42857142857142855, 3.9037819259951223, 1.293464107292913, 'HP:0033127', 'Abnormality of the musculoskeletal system'),
(313891, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0100935', 'abnormal skeleton', 0.41379310344827586, 3.9037819259951223, 1.270967363209146, 'HP:0033127', 'Abnormality of the musculoskeletal system'),
(313892, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0101220', 'abnormal centriole', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(313893, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0100481', 'abnormal anatomical line', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(313894, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0103353', 'decreased size of the muscle', 0.40476190476190477, 6.895202660022325, 1.6706032929423995, 'HP:0011805', 'Abnormal skeletal muscle morphology'),
(313895, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0131655', 'abnormal myofibril', 0.4117647058823529, 5.968280811662945, 1.5676502776568768, 'UPHENO:0002816', 'abnormal musculature'),
(313896, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0100378', 'abnormal perichondrium', 0.41379310344827586, 3.9037819259951223, 1.270967363209146, 'HP:0033127', 'Abnormality of the musculoskeletal system'),
(313897, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0131667', 'abnormal actin cytoskeleton', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(313898, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0131666', 'abnormal adherens junction', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(313899, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0100574', 'abnormal gastrula cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(313900, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0141499', 'abnormal tadpole', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(313901, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0101461', 'abnormal sperm entry point', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(313902, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0100545', 'abnormal male organism', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(313903, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0101472', 'abnormal zygote cortex', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(313904, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0100026', 'abnormal germ cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(313905, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0115505', 'dead whole organism', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(313906, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0101498', 'abnormal stage II oocyte', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(313907, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0107262', 'abnormal left-right axis', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(313908, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0100465', 'abnormal skeletal system', 0.4444444444444444, 3.9037819259951223, 1.3171993734173904, 'HP:0033127', 'Abnormality of the musculoskeletal system'),
(313909, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0100917', 'abnormal stage III oocyte', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(313910, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0102113', 'abnormal anatomical line morphology', 0.4166666666666667, 2.485033483301678, 1.0175611126818702, 'UPHENO:0076692', 'abnormal anatomical entity morphology'),
(313911, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0100549', 'abnormal mitotic cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(313912, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0100969', 'abnormal disaggregated/reaggregated ectoderm treated with activin', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(313913, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0100344', 'abnormal portion of organism substance', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(313914, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0100704', 'abnormal Merkel cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(313915, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0100599', 'abnormal adult immune system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(313916, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0101468', 'abnormal stage I oocyte', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(313917, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0101481', 'abnormal skeletal muscle satellite cell', 0.42424242424242425, 5.968280811662945, 1.591225288920281, 'UPHENO:0002816', 'abnormal musculature'),
(313918, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0101713', 'abnormal anatomical entity in vitro morphology', 0.4166666666666667, 2.485033483301678, 1.0175611126818702, 'UPHENO:0076692', 'abnormal anatomical entity morphology'),
(313919, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0100888', 'abnormal microtubule', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(313920, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0100417', 'abnormal dense regular connective tissue', 0.4444444444444444, 3.9037819259951223, 1.3171993734173904, 'HP:0033127', 'Abnormality of the musculoskeletal system'),
(313921, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0107260', 'abnormal anterior-posterior axis', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(313922, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0100289', 'abnormal chondroblast', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(313923, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0101109', 'abnormal egg cell-free extract', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(313924, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0100062', 'abnormal anatomical space', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(313925, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0100653', 'abnormal myoblast', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(313926, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0103098', 'abnormal secondary myofiber morphology', 0.425, 6.895202660022325, 1.7118589692230748, 'HP:0011805', 'Abnormal skeletal muscle morphology'),
(313927, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0101907', 'abnormal skeletal muscle morphology', 0.4594594594594595, 6.895202660022325, 1.7799062017525769, 'HP:0011805', 'Abnormal skeletal muscle morphology'),
(313928, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0101638', 'abnormal anatomical structure morphology', 0.4166666666666667, 2.485033483301678, 1.0175611126818702, 'UPHENO:0076692', 'abnormal anatomical entity morphology'),
(313929, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0100386', 'abnormal limb', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(313930, 'HP:0003716', 'Generalized muscular appearance from birth', 'XPO:0102378', 'abnormal smooth muscle morphology', 0.4473684210526316, 6.895202660022325, 1.7563302442456807, 'HP:0011805', 'Abnormal skeletal muscle morphology'),
(313931, 'HP:0025178', 'Subpleural interstitial thickening', 'XPO:0126955', 'abnormally localised oropharynx', 0.4067796610169492, 7.241224942262181, 1.7162700916117157, 'HP:0012252', 'Abnormal respiratory system morphology'),
(313932, 'HP:0025178', 'Subpleural interstitial thickening', 'XPO:0127602', 'abnormally localised pulmonary artery', 0.421875, 9.627087342903641, 2.0152983582555395, 'HP:0002088', 'Abnormal lung morphology'),
(313933, 'HP:0025178', 'Subpleural interstitial thickening', 'XPO:0139850', 'abnormally necrotic respiratory system', 0.5454545454545454, 7.241224942262181, 1.987400075328502, 'HP:0012252', 'Abnormal respiratory system morphology'),
(313934, 'HP:0025178', 'Subpleural interstitial thickening', 'XPO:0101548', 'abnormal pulmonary vein', 0.5, 9.627087342903641, 2.19397895875321, 'UPHENO:0019970', 'abnormal lung morphology'),
(313935, 'HP:0025178', 'Subpleural interstitial thickening', 'XPO:0100586', 'abnormal thyroid primordium', 0.46153846153846156, 7.241224942262181, 1.8281421770490451, 'HP:0012252', 'Abnormal respiratory system morphology'),
(313936, 'HP:0025178', 'Subpleural interstitial thickening', 'XPO:0141648', 'neoplastic lung', 0.46551724137931033, 9.627087342903641, 2.116973108564721, 'UPHENO:0019970', 'abnormal lung morphology'),
(313937, 'HP:0025178', 'Subpleural interstitial thickening', 'XPO:0125232', 'absent pharynx', 0.42105263157894735, 7.241224942262181, 1.746120504946495, 'HP:0012252', 'Abnormal respiratory system morphology'),
(313938, 'HP:0025178', 'Subpleural interstitial thickening', 'XPO:0130015', 'increased size of the respiratory system', 0.5217391304347826, 7.241224942262181, 1.9437156182576012, 'HP:0012252', 'Abnormal respiratory system morphology'),
(313939, 'HP:0025178', 'Subpleural interstitial thickening', 'XPO:0103175', 'abnormal external gill morphology', 0.4090909090909091, 7.034007514759976, 1.6963338494428049, 'UPHENO:0087433', 'abnormal respiratory system morphology'),
(313940, 'HP:0025178', 'Subpleural interstitial thickening', 'XPO:0141614', 'metaplastic larynx', 0.5106382978723404, 7.241224942262181, 1.922926618211807, 'HP:0012252', 'Abnormal respiratory system morphology'),
(313941, 'HP:0025178', 'Subpleural interstitial thickening', 'XPO:0102668', 'abnormal pharynx morphology', 0.42857142857142855, 7.241224942262181, 1.7616418813460253, 'HP:0012252', 'Abnormal respiratory system morphology'),
(313942, 'HP:0025178', 'Subpleural interstitial thickening', 'XPO:0127859', 'abnormally localised larynx', 0.4444444444444444, 7.241224942262181, 1.793968281927239, 'HP:0012252', 'Abnormal respiratory system morphology'),
(313943, 'HP:0025178', 'Subpleural interstitial thickening', 'XPO:0101638', 'abnormal anatomical structure morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(313944, 'HP:0025178', 'Subpleural interstitial thickening', 'XPO:0102436', 'abnormal larynx morphology', 0.46153846153846156, 7.241224942262181, 1.8281421770490451, 'HP:0012252', 'Abnormal respiratory system morphology'),
(313945, 'HP:0025178', 'Subpleural interstitial thickening', 'XPO:0101949', 'abnormal respiratory system morphology', 0.6153846153846154, 7.241224942262181, 2.1109567560723494, 'HP:0012252', 'Abnormal respiratory system morphology'),
(313946, 'HP:0025178', 'Subpleural interstitial thickening', 'XPO:0126197', 'absent larynx', 0.43636363636363634, 7.241224942262181, 1.777584666769093, 'HP:0012252', 'Abnormal respiratory system morphology'),
(313947, 'HP:0025178', 'Subpleural interstitial thickening', 'XPO:0100804', 'abnormal larynx', 0.5454545454545454, 7.241224942262181, 1.987400075328502, 'HP:0012252', 'Abnormal respiratory system morphology'),
(313948, 'HP:0025178', 'Subpleural interstitial thickening', 'XPO:0101713', 'abnormal anatomical entity in vitro morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(313949, 'HP:0025178', 'Subpleural interstitial thickening', 'XPO:0141593', 'edematous lung', 0.46551724137931033, 9.627087342903641, 2.116973108564721, 'HP:0002088', 'Abnormal lung morphology'),
(313950, 'HP:0025178', 'Subpleural interstitial thickening', 'XPO:0100210', 'abnormal pulmonary artery', 0.5, 9.627087342903641, 2.19397895875321, 'HP:0002088', 'Abnormal lung morphology'),
(313951, 'HP:0025178', 'Subpleural interstitial thickening', 'XPO:0101976', 'abnormal portion of organism substance morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(313952, 'HP:0025178', 'Subpleural interstitial thickening', 'XPO:0140598', 'abnormally necrotic lung', 0.4090909090909091, 9.627087342903641, 1.9845286374870066, 'HP:0002088', 'Abnormal lung morphology'),
(313953, 'HP:0025178', 'Subpleural interstitial thickening', 'XPO:0128535', 'decreased size of the respiratory system', 0.5217391304347826, 7.241224942262181, 1.9437156182576012, 'HP:0012252', 'Abnormal respiratory system morphology'),
(313954, 'HP:0025178', 'Subpleural interstitial thickening', 'XPO:0141644', 'neoplastic larynx', 0.43636363636363634, 7.241224942262181, 1.777584666769093, 'HP:0012252', 'Abnormal respiratory system morphology'),
(313955, 'HP:0025178', 'Subpleural interstitial thickening', 'XPO:0100117', 'abnormal aortic arch', 0.4067796610169492, 7.241224942262181, 1.7162700916117157, 'HP:0012252', 'Abnormal respiratory system morphology'),
(313956, 'HP:0025178', 'Subpleural interstitial thickening', 'XPO:0101036', 'abnormal pharynx', 0.5, 7.241224942262181, 1.9027907060764961, 'HP:0012252', 'Abnormal respiratory system morphology'),
(313957, 'HP:0025178', 'Subpleural interstitial thickening', 'XPO:0100875', 'abnormal oropharynx', 0.47058823529411764, 7.241224942262181, 1.8459781328463531, 'HP:0012252', 'Abnormal respiratory system morphology'),
(313958, 'HP:0025178', 'Subpleural interstitial thickening', 'XPO:0126220', 'absent pulmonary vein', 0.4090909090909091, 9.627087342903641, 1.9845286374870066, 'HP:0002088', 'Abnormal lung morphology'),
(313959, 'HP:0025178', 'Subpleural interstitial thickening', 'XPO:0102113', 'abnormal anatomical line morphology', 0.40625, 2.786899518863159, 1.0640385000262718, 'UPHENO:0015280', 'abnormal anatomical entity morphology in the independent continuant'),
(313960, 'HP:0025178', 'Subpleural interstitial thickening', 'XPO:0141178', 'abnormally necrotic larynx', 0.4067796610169492, 7.241224942262181, 1.7162700916117157, 'HP:0012252', 'Abnormal respiratory system morphology'),
(313961, 'HP:0025178', 'Subpleural interstitial thickening', 'XPO:0101329', 'abnormal pharyngeal epithelium', 0.4897959183673469, 7.241224942262181, 1.8832743880539138, 'HP:0012252', 'Abnormal respiratory system morphology'),
(313962, 'HP:0025178', 'Subpleural interstitial thickening', 'XPO:0126855', 'abnormally localised pharynx', 0.42857142857142855, 7.241224942262181, 1.7616418813460253, 'HP:0012252', 'Abnormal respiratory system morphology'),
(313963, 'HP:0025178', 'Subpleural interstitial thickening', 'XPO:0102932', 'abnormal lung morphology', 0.4909090909090909, 9.627087342903641, 2.1739422015332517, 'UPHENO:0019970', 'abnormal lung morphology'),
(313964, 'HP:0025178', 'Subpleural interstitial thickening', 'XPO:0127882', 'abnormally localised pulmonary vein', 0.421875, 9.627087342903641, 2.0152983582555395, 'HP:0002088', 'Abnormal lung morphology'),
(313965, 'HP:0500047', 'Nasolacrimal sac lymphoma', 'XPO:0102723', 'abnormal lower eyelid morphology', 0.4305555555555556, 9.23763525381927, 1.9943207311582913, 'HP:0030669', 'Abnormal ocular adnexa morphology'),
(313966, 'HP:0500047', 'Nasolacrimal sac lymphoma', 'XPO:0115526', 'abnormally incomplete structure of head', 0.40384615384615385, 4.5318002188002176, 1.3528303989641963, 'UPHENO:0087907', 'abnormal head morphology'),
(313967, 'HP:0500047', 'Nasolacrimal sac lymphoma', 'XPO:0142059', 'abnormal nasal region morphology', 0.40384615384615385, 4.5318002188002176, 1.3528303989641963, 'UPHENO:0087907', 'abnormal head morphology'),
(313968, 'HP:0500047', 'Nasolacrimal sac lymphoma', 'XPO:0102831', 'abnormal optic disc morphology', 0.4090909090909091, 6.575878401988876, 1.640162209521029, 'UPHENO:0087924', 'abnormal camera-type eye morphology'),
(313969, 'HP:0500047', 'Nasolacrimal sac lymphoma', 'XPO:0141839', 'edematous pharyngeal region', 0.40384615384615385, 4.5318002188002176, 1.3528303989641963, 'UPHENO:0087907', 'abnormal head morphology'),
(313970, 'HP:0500047', 'Nasolacrimal sac lymphoma', 'XPO:0100710', 'abnormal hyaloid vein', 0.40298507462686567, 6.575878401988876, 1.6278761772821302, 'UPHENO:0087924', 'abnormal camera-type eye morphology'),
(313971, 'HP:0500047', 'Nasolacrimal sac lymphoma', 'XPO:0101634', 'abnormal head morphology', 0.4117647058823529, 4.5318002188002176, 1.3660290568695288, 'UPHENO:0087907', 'abnormal head morphology'),
(313972, 'HP:0500047', 'Nasolacrimal sac lymphoma', 'XPO:0101483', 'abnormal nostril', 0.42105263157894735, 5.788671267106304, 1.561196743002159, 'UPHENO:0087472', 'abnormal face morphology'),
(313973, 'HP:0500047', 'Nasolacrimal sac lymphoma', 'XPO:0101315', 'abnormal hyaloid vascular plexus', 0.40298507462686567, 6.575878401988876, 1.6278761772821302, 'UPHENO:0087924', 'abnormal camera-type eye morphology'),
(313974, 'HP:0500047', 'Nasolacrimal sac lymphoma', 'XPO:0100779', 'abnormal optic choroid vascular plexus', 0.4090909090909091, 6.575878401988876, 1.640162209521029, 'UPHENO:0087924', 'abnormal camera-type eye morphology'),
(313975, 'HP:0500047', 'Nasolacrimal sac lymphoma', 'XPO:0140968', 'abnormally necrotic conjunctiva', 0.41025641025641024, 9.645995805453706, 1.9893043036433185, 'UPHENO:0087232', 'abnormal ocular surface region morphology'),
(313976, 'HP:0500047', 'Nasolacrimal sac lymphoma', 'XPO:0100420', 'abnormal choana', 0.4067796610169492, 5.788671267106304, 1.5345076525622334, 'UPHENO:0087472', 'abnormal face morphology'),
(313977, 'HP:0500047', 'Nasolacrimal sac lymphoma', 'XPO:0102657', 'abnormal conjunctiva morphology', 0.4383561643835616, 9.645995805453706, 2.056302925869292, 'UPHENO:0087232', 'abnormal ocular surface region morphology'),
(313978, 'HP:0500047', 'Nasolacrimal sac lymphoma', 'XPO:0100371', 'abnormal hyaloid blood vessel', 0.4153846153846154, 6.575878401988876, 1.652730686114997, 'UPHENO:0087924', 'abnormal camera-type eye morphology'),
(313979, 'HP:0500047', 'Nasolacrimal sac lymphoma', 'XPO:0102259', 'abnormal pharyngeal region morphology', 0.42, 4.5318002188002176, 1.3796217205799897, 'UPHENO:0087907', 'abnormal head morphology'),
(313980, 'HP:0040147', 'L-2-hydroxyglutaric acidemia', 'XPO:0141887', 'abnormal histidine metabolic process', 0.4430379746835443, 9.119292702704945, 2.010023126621389, 'HP:0004354', 'Abnormal circulating carboxylic acid concentration'),
(313981, 'HP:0040147', 'L-2-hydroxyglutaric acidemia', 'XPO:0141882', 'abnormal gamma-aminobutyric acid metabolic process', 0.45454545454545453, 9.119292702704945, 2.035959981601816, 'HP:0004354', 'Abnormal circulating carboxylic acid concentration'),
(313982, 'HP:0040147', 'L-2-hydroxyglutaric acidemia', 'XPO:0141858', 'abnormal serine family amino acid metabolic process', 0.44871794871794873, 9.119292702704945, 2.0228668555582994, 'HP:0004354', 'Abnormal circulating carboxylic acid concentration'),
(313983, 'HP:0040147', 'L-2-hydroxyglutaric acidemia', 'XPO:0141889', 'abnormal homoserine metabolic process', 0.4375, 9.119292702704945, 1.9974209765178228, 'HP:0004354', 'Abnormal circulating carboxylic acid concentration'),
(313984, 'HP:0040147', 'L-2-hydroxyglutaric acidemia', 'XPO:0141905', 'abnormal ornithine metabolic process', 0.44871794871794873, 9.119292702704945, 2.0228668555582994, 'HP:0004354', 'Abnormal circulating carboxylic acid concentration'),
(313985, 'HP:0040147', 'L-2-hydroxyglutaric acidemia', 'XPO:0141873', 'abnormal tricarboxylic acid metabolic process', 0.4861111111111111, 9.119292702704945, 2.1054665773313403, 'HP:0004354', 'Abnormal circulating carboxylic acid concentration'),
(313986, 'HP:0040147', 'L-2-hydroxyglutaric acidemia', 'XPO:0141918', 'abnormal tyrosine metabolic process', 0.4430379746835443, 9.119292702704945, 2.010023126621389, 'HP:0004354', 'Abnormal circulating carboxylic acid concentration'),
(313987, 'HP:0040147', 'L-2-hydroxyglutaric acidemia', 'XPO:0141922', 'abnormal valine metabolic process', 0.4430379746835443, 9.119292702704945, 2.010023126621389, 'HP:0004354', 'Abnormal circulating carboxylic acid concentration'),
(313988, 'HP:0040147', 'L-2-hydroxyglutaric acidemia', 'XPO:0141848', 'abnormal proline metabolic process', 0.4430379746835443, 9.119292702704945, 2.010023126621389, 'HP:0004354', 'Abnormal circulating carboxylic acid concentration'),
(313989, 'HP:0040147', 'L-2-hydroxyglutaric acidemia', 'XPO:0141843', 'abnormal alanine metabolic process', 0.44871794871794873, 9.119292702704945, 2.0228668555582994, 'HP:0004354', 'Abnormal circulating carboxylic acid concentration'),
(313990, 'HP:0040147', 'L-2-hydroxyglutaric acidemia', 'XPO:0141917', 'abnormal tryptophan metabolic process', 0.4430379746835443, 9.119292702704945, 2.010023126621389, 'HP:0004354', 'Abnormal circulating carboxylic acid concentration'),
(313991, 'HP:0040147', 'L-2-hydroxyglutaric acidemia', 'XPO:0141857', 'abnormal glycine metabolic process', 0.4375, 9.119292702704945, 1.9974209765178228, 'HP:0004354', 'Abnormal circulating carboxylic acid concentration'),
(313992, 'HP:0040147', 'L-2-hydroxyglutaric acidemia', 'XPO:0141888', 'abnormal threonine metabolic process', 0.4430379746835443, 9.119292702704945, 2.010023126621389, 'HP:0004354', 'Abnormal circulating carboxylic acid concentration'),
(313993, 'HP:0040147', 'L-2-hydroxyglutaric acidemia', 'XPO:0141893', 'abnormal isoleucine metabolic process', 0.4430379746835443, 9.119292702704945, 2.010023126621389, 'HP:0004354', 'Abnormal circulating carboxylic acid concentration'),
(313994, 'HP:0040147', 'L-2-hydroxyglutaric acidemia', 'XPO:0141847', 'abnormal arginine metabolic process', 0.4430379746835443, 9.119292702704945, 2.010023126621389, 'HP:0004354', 'Abnormal circulating carboxylic acid concentration'),
(313995, 'HP:0040147', 'L-2-hydroxyglutaric acidemia', 'XPO:0141868', 'abnormal asparagine metabolic process', 0.4430379746835443, 9.119292702704945, 2.010023126621389, 'HP:0004354', 'Abnormal circulating carboxylic acid concentration'),
(313996, 'HP:0040147', 'L-2-hydroxyglutaric acidemia', 'XPO:0141895', 'abnormal leucine metabolic process', 0.4430379746835443, 9.119292702704945, 2.010023126621389, 'HP:0004354', 'Abnormal circulating carboxylic acid concentration'),
(313997, 'HP:0040147', 'L-2-hydroxyglutaric acidemia', 'XPO:0141896', 'abnormal lysine metabolic process', 0.4430379746835443, 9.119292702704945, 2.010023126621389, 'HP:0004354', 'Abnormal circulating carboxylic acid concentration'),
(313998, 'HP:0040147', 'L-2-hydroxyglutaric acidemia', 'XPO:0141853', 'abnormal glutamate metabolic process', 0.45, 12.688487887567785, 2.3895228706596434, 'UPHENO:0078584', 'abnormal dicarboxylic acid metabolic process'),
(313999, 'HP:0040147', 'L-2-hydroxyglutaric acidemia', 'XPO:0141913', 'abnormal L-serine metabolic process', 0.4375, 9.119292702704945, 1.9974209765178228, 'HP:0004354', 'Abnormal circulating carboxylic acid concentration'),
(314000, 'HP:0040147', 'L-2-hydroxyglutaric acidemia', 'XPO:0141912', 'abnormal D-serine metabolic process', 0.4375, 9.119292702704945, 1.9974209765178228, 'HP:0004354', 'Abnormal circulating carboxylic acid concentration'),
(314001, 'HP:0040147', 'L-2-hydroxyglutaric acidemia', 'XPO:0141869', 'abnormal alpha-amino acid metabolic process', 0.4605263157894737, 9.119292702704945, 2.049310681908075, 'HP:0004354', 'Abnormal circulating carboxylic acid concentration'),
(314002, 'HP:0034812', 'Spermiation failure', 'XPO:0139754', 'abnormally necrotic testis', 0.6071428571428571, 10.680668383108486, 2.5465057467667074, 'HP:0011961', 'Non-obstructive azoospermia'),
(314003, 'HP:0034812', 'Spermiation failure', 'XPO:0130391', 'increased size of the seminiferous tubule', 0.5666666666666667, 10.680668383108486, 2.4601582775155224, 'HP:0011961', 'Non-obstructive azoospermia'),
(314004, 'HP:0034812', 'Spermiation failure', 'XPO:0130039', 'increased size of the testis', 0.576271186440678, 10.680668383108486, 2.480919474935324, 'HP:0011961', 'Non-obstructive azoospermia'),
(314005, 'HP:0034812', 'Spermiation failure', 'XPO:0102046', 'abnormal testis morphology', 0.6538461538461539, 10.680668383108486, 2.642633902530145, 'HP:0011961', 'Non-obstructive azoospermia'),
(314006, 'HP:0034812', 'Spermiation failure', 'XPO:0128913', 'decreased size of the seminiferous tubule', 0.5714285714285714, 10.680668383108486, 2.470473451802709, 'HP:0011961', 'Non-obstructive azoospermia'),
(314007, 'HP:0034812', 'Spermiation failure', 'XPO:0128559', 'decreased size of the testis', 0.53125, 10.680668383108486, 2.3820380094629856, 'HP:0011961', 'Non-obstructive azoospermia'),
(314008, 'HP:0020074', 'Crystalluria', 'XPO:0101212', 'abnormal glomeral mesenchyme', 0.40625, 5.4478002382576385, 1.4876722914648124, 'HP:0000119', 'Abnormality of the genitourinary system'),
(314009, 'HP:0020074', 'Crystalluria', 'XPO:0100761', 'abnormal ureter', 0.40540540540540543, 6.355235291121788, 1.6051313776896794, 'HP:0000079', 'Abnormality of the urinary system'),
(314010, 'HP:0020074', 'Crystalluria', 'XPO:0124921', 'absent urinary system', 0.41025641025641024, 6.355235291121788, 1.61470617044417, 'HP:0000079', 'Abnormality of the urinary system'),
(314011, 'HP:0020074', 'Crystalluria', 'XPO:0126535', 'abnormally localised urinary system', 0.42105263157894735, 6.355235291121788, 1.6358143365401303, 'HP:0000079', 'Abnormality of the urinary system'),
(314012, 'HP:0020074', 'Crystalluria', 'XPO:0100085', 'abnormal mesonephric sinus', 0.42857142857142855, 6.355235291121788, 1.6503551943819923, 'HP:0000079', 'Abnormality of the urinary system'),
(314013, 'HP:0020074', 'Crystalluria', 'XPO:0100069', 'abnormal urinary system', 0.5, 6.355235291121788, 1.7825873458433654, 'HP:0000079', 'Abnormality of the urinary system'),
(314014, 'HP:0020074', 'Crystalluria', 'XPO:0100120', 'abnormal genital system', 0.40625, 5.4478002382576385, 1.4876722914648124, 'HP:0000119', 'Abnormality of the genitourinary system'),
(314015, 'HP:0020074', 'Crystalluria', 'XPO:0101579', 'abnormal urethra', 0.40540540540540543, 6.355235291121788, 1.6051313776896794, 'HP:0000079', 'Abnormality of the urinary system'),
(314016, 'HP:0020074', 'Crystalluria', 'XPO:0101701', 'abnormal urinary system morphology', 0.42105263157894735, 6.355235291121788, 1.6358143365401303, 'HP:0000079', 'Abnormality of the urinary system'),
(314017, 'HP:0020074', 'Crystalluria', 'XPO:0100501', 'abnormal urogenital system', 0.4482758620689655, 5.4478002382576385, 1.562727534851952, 'HP:0000119', 'Abnormality of the genitourinary system'),
(314018, 'HP:0030632', 'Hypoautofluorescent macular lesion', 'XPO:0126243', 'absent optic choroid vascular plexus', 0.40789473684210525, 6.887869297006056, 1.6761639640277146, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(314019, 'HP:0030632', 'Hypoautofluorescent macular lesion', 'XPO:0141337', 'increased pigmentation in the eye', 0.44285714285714284, 6.887869297006056, 1.7465228647932265, 'HP:0012372', 'Abnormal eye morphology'),
(314020, 'HP:0030632', 'Hypoautofluorescent macular lesion', 'XPO:0102003', 'abnormal hyaloid blood vessel morphology', 0.4305555555555556, 6.887869297006056, 1.7220947685207388, 'HP:0012372', 'Abnormal eye morphology'),
(314021, 'HP:0030632', 'Hypoautofluorescent macular lesion', 'XPO:0141638', 'neoplastic eye', 0.44285714285714284, 6.887869297006056, 1.7465228647932265, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(314022, 'HP:0030632', 'Hypoautofluorescent macular lesion', 'XPO:0140335', 'abnormally necrotic pharyngeal region', 0.4117647058823529, 4.5318002188002176, 1.3660290568695288, 'UPHENO:0087907', 'abnormal head morphology'),
(314023, 'HP:0030632', 'Hypoautofluorescent macular lesion', 'XPO:0133354', 'fused eyes', 0.44285714285714284, 6.887869297006056, 1.7465228647932265, 'HP:0012372', 'Abnormal eye morphology'),
(314024, 'HP:0030632', 'Hypoautofluorescent macular lesion', 'XPO:0140218', 'abnormally necrotic sclera', 0.4246575342465753, 6.887869297006056, 1.7102589253909142, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(314025, 'HP:0030632', 'Hypoautofluorescent macular lesion', 'XPO:0102259', 'abnormal pharyngeal region morphology', 0.4375, 4.5318002188002176, 1.4080705222839853, 'UPHENO:0087907', 'abnormal head morphology'),
(314026, 'HP:0030632', 'Hypoautofluorescent macular lesion', 'XPO:0100329', 'abnormal retinal blood vessel', 0.4857142857142857, 7.726220534922893, 1.9371978960320806, 'UPHENO:0021037', 'abnormal posterior segment of eyeball morphology'),
(314027, 'HP:0030632', 'Hypoautofluorescent macular lesion', 'XPO:0101861', 'abnormal photoreceptor layer morphology', 0.40476190476190477, 7.726220534922893, 1.7684116433471968, 'UPHENO:0021037', 'abnormal posterior segment of eyeball morphology'),
(314028, 'HP:0030632', 'Hypoautofluorescent macular lesion', 'XPO:0128643', 'decreased size of the retinal layer', 0.4473684210526316, 7.726220534922893, 1.8591576268334198, 'UPHENO:0021037', 'abnormal posterior segment of eyeball morphology'),
(314029, 'HP:0030632', 'Hypoautofluorescent macular lesion', 'XPO:0139887', 'abnormally necrotic Muller cell', 0.40476190476190477, 7.726220534922893, 1.7684116433471968, 'UPHENO:0021037', 'abnormal posterior segment of eyeball morphology'),
(314030, 'HP:0030632', 'Hypoautofluorescent macular lesion', 'XPO:0101634', 'abnormal head morphology', 0.42857142857142855, 4.5318002188002176, 1.3936283915633758, 'UPHENO:0087907', 'abnormal head morphology'),
(314031, 'HP:0030632', 'Hypoautofluorescent macular lesion', 'XPO:0100371', 'abnormal hyaloid blood vessel', 0.5254237288135594, 6.887869297006056, 1.9023800802188169, 'HP:0012372', 'Abnormal eye morphology'),
(314032, 'HP:0030632', 'Hypoautofluorescent macular lesion', 'XPO:0102756', 'abnormal Muller cell morphology', 0.43037974683544306, 7.726220534922893, 1.8235155161980159, 'UPHENO:0021037', 'abnormal posterior segment of eyeball morphology'),
(314033, 'HP:0030632', 'Hypoautofluorescent macular lesion', 'XPO:0103210', 'abnormal pupil morphology', 0.4025974025974026, 6.887869297006056, 1.6652442128423794, 'HP:0012372', 'Abnormal eye morphology'),
(314034, 'HP:0030632', 'Hypoautofluorescent macular lesion', 'XPO:0102831', 'abnormal optic disc morphology', 0.421875, 6.575878401988876, 1.6655925974976766, 'UPHENO:0087924', 'abnormal camera-type eye morphology'),
(314035, 'HP:0030632', 'Hypoautofluorescent macular lesion', 'XPO:0102117', 'abnormal retina morphology', 0.4788732394366197, 7.726220534922893, 1.9235072799862907, 'UPHENO:0021037', 'abnormal posterior segment of eyeball morphology'),
(314036, 'HP:0030632', 'Hypoautofluorescent macular lesion', 'XPO:0103186', 'abnormal peripheral retina morphology', 0.4594594594594595, 7.726220534922893, 1.8841138794245555, 'UPHENO:0021037', 'abnormal posterior segment of eyeball morphology'),
(314037, 'HP:0030632', 'Hypoautofluorescent macular lesion', 'XPO:0127645', 'abnormally localised hyaloid vein', 0.4305555555555556, 6.887869297006056, 1.7220947685207388, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(314038, 'HP:0030632', 'Hypoautofluorescent macular lesion', 'XPO:0140375', 'abnormally necrotic lens', 0.40789473684210525, 6.887869297006056, 1.6761639640277146, 'HP:0012372', 'Abnormal eye morphology'),
(314039, 'HP:0030632', 'Hypoautofluorescent macular lesion', 'XPO:0140487', 'abnormally necrotic retinal layer', 0.4533333333333333, 7.726220534922893, 1.871510969555093, 'UPHENO:0021037', 'abnormal posterior segment of eyeball morphology'),
(314040, 'HP:0030632', 'Hypoautofluorescent macular lesion', 'XPO:0102663', 'abnormal retinal progenitor cell morphology', 0.40476190476190477, 7.726220534922893, 1.7684116433471968, 'UPHENO:0021037', 'abnormal posterior segment of eyeball morphology'),
(314041, 'HP:0030632', 'Hypoautofluorescent macular lesion', 'XPO:0140531', 'abnormally necrotic retinal progenitor cell region', 0.4358974358974359, 7.726220534922893, 1.8351674910893023, 'UPHENO:0021037', 'abnormal posterior segment of eyeball morphology'),
(314042, 'HP:0030632', 'Hypoautofluorescent macular lesion', 'XPO:0128935', 'decreased size of the central retina', 0.4473684210526316, 7.726220534922893, 1.8591576268334198, 'UPHENO:0021037', 'abnormal posterior segment of eyeball morphology'),
(314043, 'HP:0030632', 'Hypoautofluorescent macular lesion', 'XPO:0130863', 'increased size of the sclera', 0.41333333333333333, 6.887869297006056, 1.6873013886368484, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(314044, 'HP:0030632', 'Hypoautofluorescent macular lesion', 'XPO:0133369', 'eye fused with brain', 0.44285714285714284, 6.887869297006056, 1.7465228647932265, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(314045, 'HP:0030632', 'Hypoautofluorescent macular lesion', 'XPO:0102196', 'abnormal central retina morphology', 0.4788732394366197, 7.726220534922893, 1.9235072799862907, 'UPHENO:0021037', 'abnormal posterior segment of eyeball morphology'),
(314046, 'HP:0030632', 'Hypoautofluorescent macular lesion', 'XPO:0101483', 'abnormal nostril', 0.43636363636363634, 5.788671267106304, 1.589328677092377, 'UPHENO:0087472', 'abnormal face morphology'),
(314047, 'HP:0030632', 'Hypoautofluorescent macular lesion', 'XPO:0141343', 'decreased pigmentation in the eye', 0.44285714285714284, 6.887869297006056, 1.7465228647932265, 'HP:0012372', 'Abnormal eye morphology'),
(314048, 'HP:0030632', 'Hypoautofluorescent macular lesion', 'XPO:0140271', 'abnormally necrotic peripheral retina', 0.425, 7.726220534922893, 1.812082704332843, 'UPHENO:0021037', 'abnormal posterior segment of eyeball morphology'),
(314049, 'HP:0030632', 'Hypoautofluorescent macular lesion', 'XPO:0130265', 'increased size of the peripheral retina', 0.4146341463414634, 7.726220534922893, 1.7898477186463766, 'UPHENO:0021037', 'abnormal posterior segment of eyeball morphology'),
(314050, 'HP:0030632', 'Hypoautofluorescent macular lesion', 'XPO:0128300', 'decreased size of the retina', 0.4358974358974359, 7.726220534922893, 1.8351674910893023, 'UPHENO:0021037', 'abnormal posterior segment of eyeball morphology'),
(314051, 'HP:0030632', 'Hypoautofluorescent macular lesion', 'XPO:0141298', 'abnormal intercanthal region morphology', 0.4117647058823529, 4.5318002188002176, 1.3660290568695288, 'UPHENO:0087907', 'abnormal head morphology'),
(314052, 'HP:0030632', 'Hypoautofluorescent macular lesion', 'XPO:0128475', 'decreased size of the retinal stem cell region', 0.425, 7.726220534922893, 1.812082704332843, 'UPHENO:0021037', 'abnormal posterior segment of eyeball morphology'),
(314053, 'HP:0030632', 'Hypoautofluorescent macular lesion', 'XPO:0127563', 'abnormally localised retinal blood vessel', 0.425, 7.726220534922893, 1.812082704332843, 'UPHENO:0021037', 'abnormal posterior segment of eyeball morphology'),
(314054, 'HP:0030632', 'Hypoautofluorescent macular lesion', 'XPO:0103101', 'abnormal medial nasal prominence morphology', 0.40384615384615385, 4.5318002188002176, 1.3528303989641963, 'UPHENO:0087907', 'abnormal head morphology'),
(314055, 'HP:0030632', 'Hypoautofluorescent macular lesion', 'XPO:0101359', 'abnormal hyaloid artery', 0.41333333333333333, 6.887869297006056, 1.6873013886368484, 'HP:0012372', 'Abnormal eye morphology'),
(314056, 'HP:0030632', 'Hypoautofluorescent macular lesion', 'XPO:0128787', 'decreased size of the peripheral retina', 0.4146341463414634, 7.726220534922893, 1.7898477186463766, 'UPHENO:0021037', 'abnormal posterior segment of eyeball morphology'),
(314057, 'HP:0030632', 'Hypoautofluorescent macular lesion', 'XPO:0101817', 'abnormal eye morphology', 0.4626865671641791, 6.887869297006056, 1.7851959556606887, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(314058, 'HP:0030632', 'Hypoautofluorescent macular lesion', 'XPO:0103048', 'abnormal cornea morphology', 0.41333333333333333, 6.887869297006056, 1.6873013886368484, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(314059, 'HP:0030632', 'Hypoautofluorescent macular lesion', 'XPO:0129955', 'increased size of the retinal stem cell region', 0.425, 7.726220534922893, 1.812082704332843, 'UPHENO:0021037', 'abnormal posterior segment of eyeball morphology'),
(314060, 'HP:0030632', 'Hypoautofluorescent macular lesion', 'XPO:0129388', 'decreased size of the sclera', 0.41333333333333333, 6.887869297006056, 1.6873013886368484, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(314061, 'HP:0030632', 'Hypoautofluorescent macular lesion', 'XPO:0141839', 'edematous pharyngeal region', 0.42, 4.5318002188002176, 1.3796217205799897, 'UPHENO:0087907', 'abnormal head morphology'),
(314062, 'HP:0030632', 'Hypoautofluorescent macular lesion', 'XPO:0100420', 'abnormal choana', 0.42105263157894735, 5.788671267106304, 1.561196743002159, 'UPHENO:0087472', 'abnormal face morphology'),
(314063, 'HP:0030632', 'Hypoautofluorescent macular lesion', 'XPO:0127907', 'abnormally localised optic choroid vascular plexus', 0.43661971830985913, 6.887869297006056, 1.734179792355427, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(314064, 'HP:0030632', 'Hypoautofluorescent macular lesion', 'XPO:0115423', 'abnormally incomplete structure of eye', 0.45588235294117646, 6.887869297006056, 1.7720208976957377, 'HP:0012372', 'Abnormal eye morphology'),
(314065, 'HP:0030632', 'Hypoautofluorescent macular lesion', 'XPO:0129810', 'increased size of the retinal progenitor cell region', 0.425, 7.726220534922893, 1.812082704332843, 'UPHENO:0021037', 'abnormal posterior segment of eyeball morphology'),
(314066, 'HP:0030632', 'Hypoautofluorescent macular lesion', 'XPO:0102450', 'abnormal retinal stem cell morphology', 0.40476190476190477, 7.726220534922893, 1.7684116433471968, 'UPHENO:0021037', 'abnormal posterior segment of eyeball morphology'),
(314067, 'HP:0030632', 'Hypoautofluorescent macular lesion', 'XPO:0133372', 'eye fused with olfactory epithelium', 0.44285714285714284, 6.887869297006056, 1.7465228647932265, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(314068, 'HP:0030632', 'Hypoautofluorescent macular lesion', 'XPO:0140538', 'abnormally necrotic optic disc', 0.40298507462686567, 6.575878401988876, 1.6278761772821302, 'UPHENO:0087924', 'abnormal camera-type eye morphology'),
(314069, 'HP:0030632', 'Hypoautofluorescent macular lesion', 'XPO:0102734', 'abnormal craniofacial region morphology', 0.40384615384615385, 4.5318002188002176, 1.3528303989641963, 'UPHENO:0087907', 'abnormal head morphology'),
(314070, 'HP:0030632', 'Hypoautofluorescent macular lesion', 'XPO:0130413', 'increased size of the central retina', 0.4473684210526316, 7.726220534922893, 1.8591576268334198, 'UPHENO:0021037', 'abnormal posterior segment of eyeball morphology'),
(314071, 'HP:0030632', 'Hypoautofluorescent macular lesion', 'XPO:0141339', 'decreased pigmentation in the head', 0.40384615384615385, 4.5318002188002176, 1.3528303989641963, 'UPHENO:0087907', 'abnormal head morphology'),
(314072, 'HP:0030632', 'Hypoautofluorescent macular lesion', 'XPO:0140192', 'abnormally necrotic retina', 0.4473684210526316, 7.726220534922893, 1.8591576268334198, 'UPHENO:0021037', 'abnormal posterior segment of eyeball morphology'),
(314073, 'HP:0030632', 'Hypoautofluorescent macular lesion', 'XPO:0139731', 'abnormally necrotic eye', 0.4189189189189189, 6.887869297006056, 1.6986638159319787, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(314074, 'HP:0030632', 'Hypoautofluorescent macular lesion', 'XPO:0128330', 'decreased size of the retinal progenitor cell region', 0.425, 7.726220534922893, 1.812082704332843, 'UPHENO:0021037', 'abnormal posterior segment of eyeball morphology'),
(314075, 'HP:0030632', 'Hypoautofluorescent macular lesion', 'XPO:0102162', 'abnormal ciliary marginal zone morphology', 0.43037974683544306, 7.726220534922893, 1.8235155161980159, 'UPHENO:0021037', 'abnormal posterior segment of eyeball morphology'),
(314076, 'HP:0030632', 'Hypoautofluorescent macular lesion', 'XPO:0126122', 'absent hyaloid vascular plexus', 0.40789473684210525, 6.887869297006056, 1.6761639640277146, 'HP:0012372', 'Abnormal eye morphology'),
(314077, 'HP:0030632', 'Hypoautofluorescent macular lesion', 'XPO:0115526', 'abnormally incomplete structure of head', 0.42, 4.5318002188002176, 1.3796217205799897, 'UPHENO:0087907', 'abnormal head morphology'),
(314078, 'HP:0030632', 'Hypoautofluorescent macular lesion', 'XPO:0129780', 'increased size of the retina', 0.4358974358974359, 7.726220534922893, 1.8351674910893023, 'UPHENO:0021037', 'abnormal posterior segment of eyeball morphology'),
(314079, 'HP:0030632', 'Hypoautofluorescent macular lesion', 'XPO:0125990', 'absent hyaloid vein', 0.41333333333333333, 6.887869297006056, 1.6873013886368484, 'HP:0012372', 'Abnormal eye morphology'),
(314080, 'HP:0030632', 'Hypoautofluorescent macular lesion', 'XPO:0115417', 'abnormally wholly ventralized eye', 0.4189189189189189, 6.887869297006056, 1.6986638159319787, 'HP:0012372', 'Abnormal eye morphology'),
(314081, 'HP:0030632', 'Hypoautofluorescent macular lesion', 'XPO:0102476', 'abnormal lens transitional zone morphology', 0.4246575342465753, 6.887869297006056, 1.7102589253909142, 'HP:0012372', 'Abnormal eye morphology'),
(314082, 'HP:0030632', 'Hypoautofluorescent macular lesion', 'XPO:0102805', 'abnormal retinal layer morphology', 0.4927536231884058, 7.726220534922893, 1.9511850660908407, 'UPHENO:0021037', 'abnormal posterior segment of eyeball morphology'),
(314083, 'HP:0030632', 'Hypoautofluorescent macular lesion', 'XPO:0102017', 'abnormal retinal neural layer morphology', 0.40476190476190477, 7.726220534922893, 1.7684116433471968, 'UPHENO:0021037', 'abnormal posterior segment of eyeball morphology'),
(314084, 'HP:0030632', 'Hypoautofluorescent macular lesion', 'XPO:0102550', 'abnormal lens morphology', 0.43661971830985913, 6.887869297006056, 1.734179792355427, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(314085, 'HP:0030632', 'Hypoautofluorescent macular lesion', 'XPO:0102212', 'abnormal globe morphology', 0.4090909090909091, 6.575878401988876, 1.640162209521029, 'UPHENO:0087924', 'abnormal camera-type eye morphology'),
(314086, 'HP:0030632', 'Hypoautofluorescent macular lesion', 'XPO:0101315', 'abnormal hyaloid vascular plexus', 0.5081967213114754, 6.887869297006056, 1.87093361548732, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(314087, 'HP:0030632', 'Hypoautofluorescent macular lesion', 'XPO:0102513', 'abnormal sclera morphology', 0.45588235294117646, 6.887869297006056, 1.7720208976957377, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(314088, 'HP:0030632', 'Hypoautofluorescent macular lesion', 'XPO:0102862', 'abnormal iris morphology', 0.4025974025974026, 6.887869297006056, 1.6652442128423794, 'HP:0012372', 'Abnormal eye morphology'),
(314089, 'HP:0030632', 'Hypoautofluorescent macular lesion', 'XPO:0140391', 'abnormally necrotic central retina', 0.4594594594594595, 7.726220534922893, 1.8841138794245555, 'UPHENO:0021037', 'abnormal posterior segment of eyeball morphology'),
(314090, 'HP:0030632', 'Hypoautofluorescent macular lesion', 'XPO:0127783', 'abnormally localised hyaloid vascular plexus', 0.4246575342465753, 6.887869297006056, 1.7102589253909142, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(314091, 'HP:0030632', 'Hypoautofluorescent macular lesion', 'XPO:0103707', 'increased pigmentation in the head', 0.40384615384615385, 4.5318002188002176, 1.3528303989641963, 'UPHENO:0087907', 'abnormal head morphology'),
(314092, 'HP:0030632', 'Hypoautofluorescent macular lesion', 'XPO:0102538', 'abnormal lateral nasal prominence morphology', 0.40384615384615385, 4.5318002188002176, 1.3528303989641963, 'UPHENO:0087907', 'abnormal head morphology'),
(314093, 'HP:0030632', 'Hypoautofluorescent macular lesion', 'XPO:0103022', 'abnormal ciliary body morphology', 0.41333333333333333, 6.887869297006056, 1.6873013886368484, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(314094, 'HP:0030632', 'Hypoautofluorescent macular lesion', 'XPO:0100710', 'abnormal hyaloid vein', 0.5081967213114754, 6.887869297006056, 1.87093361548732, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(314095, 'HP:0030632', 'Hypoautofluorescent macular lesion', 'XPO:0100779', 'abnormal optic choroid vascular plexus', 0.5166666666666667, 6.887869297006056, 1.886460301760892, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(314096, 'HP:0030632', 'Hypoautofluorescent macular lesion', 'XPO:0140553', 'abnormally necrotic retinal stem cell region', 0.4358974358974359, 7.726220534922893, 1.8351674910893023, 'UPHENO:0021037', 'abnormal posterior segment of eyeball morphology'),
(314097, 'HP:0030632', 'Hypoautofluorescent macular lesion', 'XPO:0133371', 'eye fused with olfactory pit', 0.44285714285714284, 6.887869297006056, 1.7465228647932265, 'HP:0012372', 'Abnormal eye morphology'),
(314098, 'HP:0030632', 'Hypoautofluorescent macular lesion', 'XPO:0130122', 'increased size of the retinal layer', 0.4473684210526316, 7.726220534922893, 1.8591576268334198, 'UPHENO:0021037', 'abnormal posterior segment of eyeball morphology'),
(314099, 'HP:0030632', 'Hypoautofluorescent macular lesion', 'XPO:0102505', 'abnormal retinal stem cell region morphology', 0.4533333333333333, 7.726220534922893, 1.871510969555093, 'UPHENO:0021037', 'abnormal posterior segment of eyeball morphology'),
(314100, 'HP:0030632', 'Hypoautofluorescent macular lesion', 'XPO:0102804', 'abnormal pharyngeal pouch morphology', 0.40384615384615385, 4.5318002188002176, 1.3528303989641963, 'UPHENO:0087907', 'abnormal head morphology'),
(314101, 'HP:0030632', 'Hypoautofluorescent macular lesion', 'XPO:0142059', 'abnormal nasal region morphology', 0.42, 4.5318002188002176, 1.3796217205799897, 'UPHENO:0087907', 'abnormal head morphology'),
(314102, 'HP:0030632', 'Hypoautofluorescent macular lesion', 'XPO:0125589', 'absent hyaloid blood vessel', 0.43661971830985913, 6.887869297006056, 1.734179792355427, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(314103, 'HP:0030632', 'Hypoautofluorescent macular lesion', 'XPO:0127230', 'abnormally localised hyaloid blood vessel', 0.45588235294117646, 6.887869297006056, 1.7720208976957377, 'HP:0012372', 'Abnormal eye morphology'),
(314104, 'HP:0030632', 'Hypoautofluorescent macular lesion', 'XPO:0141323', 'edematous eye', 0.4492753623188406, 6.887869297006056, 1.759133301946505, 'UPHENO:0021474', 'abnormal camera-type eye morphology'),
(314105, 'HP:0030632', 'Hypoautofluorescent macular lesion', 'XPO:0102784', 'abnormal retinal progenitor cell region morphology', 0.4533333333333333, 7.726220534922893, 1.871510969555093, 'UPHENO:0021037', 'abnormal posterior segment of eyeball morphology'),
(314106, 'HP:0030632', 'Hypoautofluorescent macular lesion', 'XPO:0141835', 'edematous head', 0.4117647058823529, 4.5318002188002176, 1.3660290568695288, 'UPHENO:0087907', 'abnormal head morphology'),
(314107, 'HP:0030632', 'Hypoautofluorescent macular lesion', 'XPO:0102818', 'abnormal optic chiasm morphology', 0.4146341463414634, 7.726220534922893, 1.7898477186463766, 'UPHENO:0021037', 'abnormal posterior segment of eyeball morphology'),
(314108, 'HP:0400000', 'Tall chin', 'XPO:0129225', 'decreased size of the upper jaw', 0.42168674698795183, 7.312692920701687, 1.7560369271323764, 'UPHENO:0076800', 'abnormal mouth morphology'),
(314109, 'HP:0400000', 'Tall chin', 'XPO:0101816', 'abnormal tooth morphology', 0.4024390243902439, 7.312692920701687, 1.7154920590526295, 'UPHENO:0076800', 'abnormal mouth morphology'),
(314110, 'HP:0400000', 'Tall chin', 'XPO:0102223', 'abnormal pharyngeal arch morphology', 0.4426229508196721, 5.725717590856133, 1.5919591752381232, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(314111, 'HP:0400000', 'Tall chin', 'XPO:0103711', 'increased size of the alimentary system', 0.41379310344827586, 5.972749669260594, 1.572094978607528, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(314112, 'HP:0400000', 'Tall chin', 'XPO:0129152', 'decreased size of the oral cavity', 0.5074626865671642, 7.312692920701687, 1.9263745211095273, 'UPHENO:0076800', 'abnormal mouth morphology'),
(314113, 'HP:0400000', 'Tall chin', 'XPO:0140897', 'abnormally necrotic lower jaw', 0.425, 7.312692920701687, 1.7629221455578283, 'UPHENO:0076800', 'abnormal mouth morphology'),
(314114, 'HP:0400000', 'Tall chin', 'XPO:0128880', 'decreased size of the lower jaw', 0.43209876543209874, 7.312692920701687, 1.7775841985737968, 'UPHENO:0076800', 'abnormal mouth morphology'),
(314115, 'HP:0400000', 'Tall chin', 'XPO:0130241', 'increased size of the branchial arch 1', 0.410958904109589, 5.972749669260594, 1.5667018410023792, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(314116, 'HP:0400000', 'Tall chin', 'XPO:0130034', 'increased size of the branchial arch 2', 0.410958904109589, 5.972749669260594, 1.5667018410023792, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(314117, 'HP:0400000', 'Tall chin', 'XPO:0128105', 'decreased size of the tongue', 0.4533333333333333, 7.312692920701687, 1.8207381627748578, 'UPHENO:0076800', 'abnormal mouth morphology'),
(314118, 'HP:0400000', 'Tall chin', 'XPO:0140639', 'abnormally necrotic upper jaw', 0.4146341463414634, 7.312692920701687, 1.7412903797564627, 'UPHENO:0076800', 'abnormal mouth morphology'),
(314119, 'HP:0400000', 'Tall chin', 'XPO:0131573', 'decreased size of the roof of mouth', 0.4857142857142857, 7.312692920701687, 1.884643048066804, 'UPHENO:0076800', 'abnormal mouth morphology'),
(314120, 'HP:0400000', 'Tall chin', 'XPO:0102261', 'abnormal branchial arch 2 morphology', 0.4090909090909091, 5.725717590856133, 1.5304701939081158, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(314121, 'HP:0400000', 'Tall chin', 'XPO:0103096', 'abnormal oral cavity morphology', 0.5238095238095238, 7.312692920701687, 1.9571556393291838, 'UPHENO:0076800', 'abnormal mouth morphology'),
(314122, 'HP:0400000', 'Tall chin', 'XPO:0141009', 'abnormally necrotic oral epithelium', 0.42857142857142855, 7.312692920701687, 1.7703138850862843, 'UPHENO:0076800', 'abnormal mouth morphology'),
(314123, 'HP:0400000', 'Tall chin', 'XPO:0102204', 'abnormal branchial arch morphology', 0.42857142857142855, 5.725717590856133, 1.5664861849086864, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(314124, 'HP:0400000', 'Tall chin', 'XPO:0102203', 'abnormal branchial arch 1 morphology', 0.4090909090909091, 5.725717590856133, 1.5304701939081158, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(314125, 'HP:0400000', 'Tall chin', 'XPO:0129585', 'increased size of the tongue', 0.46153846153846156, 7.312692920701687, 1.8371415406342146, 'UPHENO:0076800', 'abnormal mouth morphology'),
(314126, 'HP:0400000', 'Tall chin', 'XPO:0130701', 'increased size of the upper jaw', 0.4567901234567901, 7.312692920701687, 1.8276667918548277, 'UPHENO:0076800', 'abnormal mouth morphology'),
(314127, 'HP:0400000', 'Tall chin', 'XPO:0115393', 'abnormally decreased volume of oral cavity', 0.4927536231884058, 7.312692920701687, 1.8982507558117714, 'UPHENO:0076800', 'abnormal mouth morphology'),
(314128, 'HP:0400000', 'Tall chin', 'XPO:0101659', 'abnormal lower jaw morphology', 0.4533333333333333, 7.312692920701687, 1.8207381627748578, 'UPHENO:0076800', 'abnormal mouth morphology'),
(314129, 'HP:0400000', 'Tall chin', 'XPO:0103828', 'decreased width of the mouth', 0.4473684210526316, 7.312692920701687, 1.8087199577538449, 'UPHENO:0076800', 'abnormal mouth morphology'),
(314130, 'HP:0400000', 'Tall chin', 'XPO:0103357', 'decreased size of the pharyngeal arch', 0.4117647058823529, 5.725717590856133, 1.5354635846428564, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(314131, 'HP:0400000', 'Tall chin', 'XPO:0141830', 'increased width of mouth', 0.4864864864864865, 7.312692920701687, 1.8861405795292054, 'UPHENO:0076800', 'abnormal mouth morphology'),
(314132, 'HP:0400000', 'Tall chin', 'XPO:0102445', 'abnormal branchial arch 3 morphology', 0.4153846153846154, 5.725717590856133, 1.5421981063659433, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(314133, 'HP:0400000', 'Tall chin', 'XPO:0130062', 'increased size of the head region', 0.4067796610169492, 5.972749669260594, 1.5587152035573786, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(314134, 'HP:0400000', 'Tall chin', 'XPO:0103199', 'abnormal tongue morphology', 0.5238095238095238, 7.312692920701687, 1.9571556393291838, 'UPHENO:0076800', 'abnormal mouth morphology'),
(314135, 'HP:0400000', 'Tall chin', 'XPO:0130358', 'increased size of the lower jaw', 0.46835443037974683, 7.312692920701687, 1.8506572149961338, 'UPHENO:0076800', 'abnormal mouth morphology'),
(314136, 'HP:0400000', 'Tall chin', 'XPO:0139863', 'abnormally necrotic pharyngeal arch', 0.4090909090909091, 5.725717590856133, 1.5304701939081158, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(314137, 'HP:0400000', 'Tall chin', 'XPO:0140789', 'abnormally necrotic roof of mouth', 0.4782608695652174, 7.312692920701687, 1.8701269676463677, 'UPHENO:0076800', 'abnormal mouth morphology'),
(314138, 'HP:0400000', 'Tall chin', 'XPO:0127750', 'abnormally localised tongue', 0.4626865671641791, 7.312692920701687, 1.8394251232940302, 'UPHENO:0076800', 'abnormal mouth morphology'),
(314139, 'HP:0400000', 'Tall chin', 'XPO:0115558', 'abnormally incomplete structure of mouth', 0.532258064516129, 7.312692920701687, 1.9728760174865216, 'UPHENO:0076800', 'abnormal mouth morphology'),
(314140, 'HP:0400000', 'Tall chin', 'XPO:0102525', 'abnormal hyoid arch morphology', 0.421875, 5.725717590856133, 1.554199829057522, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(314141, 'HP:0400000', 'Tall chin', 'XPO:0129644', 'increased size of the branchial arch 3', 0.4166666666666667, 5.972749669260594, 1.5775441976455835, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(314142, 'HP:0400000', 'Tall chin', 'XPO:0103138', 'abnormal upper jaw morphology', 0.44155844155844154, 7.312692920701687, 1.7969366404134801, 'UPHENO:0076800', 'abnormal mouth morphology'),
(314143, 'HP:0400000', 'Tall chin', 'XPO:0129821', 'increased size of the pharyngeal cavity', 0.42857142857142855, 5.972749669260594, 1.5999218287949384, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(314144, 'HP:0400000', 'Tall chin', 'XPO:0131611', 'increased size of the roof of mouth', 0.5294117647058824, 7.312692920701687, 1.9675938767695158, 'UPHENO:0076800', 'abnormal mouth morphology'),
(314145, 'HP:0400000', 'Tall chin', 'XPO:0101567', 'abnormal tongue', 0.5263157894736842, 7.312692920701687, 1.96183224250641, 'UPHENO:0076800', 'abnormal mouth morphology'),
(314146, 'HP:0400000', 'Tall chin', 'XPO:0102420', 'abnormal branchial arch 4 morphology', 0.4090909090909091, 5.725717590856133, 1.5304701939081158, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(314147, 'HP:0400000', 'Tall chin', 'XPO:0130340', 'increased size of the pharyngeal mesenchyme', 0.42857142857142855, 5.972749669260594, 1.5999218287949384, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(314148, 'HP:0400000', 'Tall chin', 'XPO:0103352', 'decreased size of the mouth', 0.4788732394366197, 7.312692920701687, 1.8713238490281827, 'UPHENO:0076800', 'abnormal mouth morphology'),
(314149, 'HP:0400000', 'Tall chin', 'XPO:0130132', 'increased size of the oral epithelium', 0.47368421052631576, 7.312692920701687, 1.8611574820428165, 'UPHENO:0076800', 'abnormal mouth morphology'),
(314150, 'HP:0400000', 'Tall chin', 'XPO:0102279', 'abnormal mouth morphology', 0.5409836065573771, 7.312692920701687, 1.9889813950582338, 'UPHENO:0076800', 'abnormal mouth morphology'),
(314151, 'HP:0400000', 'Tall chin', 'XPO:0102735', 'abnormal pharyngeal mesenchyme morphology', 0.4153846153846154, 5.725717590856133, 1.5421981063659433, 'UPHENO:0076803', 'abnormal digestive system morphology'),
(314152, 'HP:0400000', 'Tall chin', 'XPO:0131638', 'increased size of the intercanthal region', 0.4067796610169492, 5.972749669260594, 1.5587152035573786, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(314153, 'HP:0400000', 'Tall chin', 'XPO:0128653', 'decreased size of the oral epithelium', 0.4358974358974359, 7.312692920701687, 1.7853806579100147, 'UPHENO:0076800', 'abnormal mouth morphology'),
(314154, 'HP:0400000', 'Tall chin', 'XPO:0103739', 'increased size of the pharyngeal region', 0.42857142857142855, 5.972749669260594, 1.5999218287949384, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(314155, 'HP:0400000', 'Tall chin', 'XPO:0130133', 'increased size of the hyoid arch', 0.42857142857142855, 5.972749669260594, 1.5999218287949384, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(314156, 'HP:0400000', 'Tall chin', 'XPO:0126089', 'absent tongue', 0.4492753623188406, 7.312692920701687, 1.812570760404865, 'UPHENO:0076800', 'abnormal mouth morphology'),
(314157, 'HP:0400000', 'Tall chin', 'XPO:0102960', 'abnormal oral epithelium morphology', 0.4714285714285714, 7.312692920701687, 1.856720866716972, 'UPHENO:0076800', 'abnormal mouth morphology'),
(314158, 'HP:0400000', 'Tall chin', 'XPO:0103738', 'increased size of the pharyngeal arch', 0.45454545454545453, 5.972749669260594, 1.6476911765559314, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(314159, 'HP:0400000', 'Tall chin', 'XPO:0103714', 'increased size of the branchial arch', 0.43478260869565216, 5.972749669260594, 1.6114737609676475, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(314160, 'HP:0400000', 'Tall chin', 'XPO:0130628', 'increased size of the oral cavity', 0.5538461538461539, 7.312692920701687, 2.0124877262703063, 'UPHENO:0076800', 'abnormal mouth morphology'),
(314161, 'HP:0400000', 'Tall chin', 'XPO:0130525', 'increased size of the branchial arch 4', 0.410958904109589, 5.972749669260594, 1.5667018410023792, 'UPHENO:0065599', 'increased size of the anatomical entity in independent continuant'),
(314162, 'HP:0400000', 'Tall chin', 'XPO:0141311', 'abnormal roof of mouth morphology', 0.515625, 7.312692920701687, 1.9418051620172418, 'UPHENO:0076800', 'abnormal mouth morphology'),
(314163, 'HP:0400000', 'Tall chin', 'XPO:0103735', 'increased size of the mouth', 0.5217391304347826, 7.312692920701687, 1.953283913204501, 'UPHENO:0076800', 'abnormal mouth morphology'),
(314164, 'HP:0400000', 'Tall chin', 'XPO:0140626', 'abnormally necrotic tongue', 0.4852941176470588, 7.312692920701687, 1.8838277146745184, 'UPHENO:0076800', 'abnormal mouth morphology'),
(314165, 'HP:0025047', 'Abnormal brain choline level by MRS', 'XPO:0100032', 'abnormal nervous system', 0.48148148148148145, 3.94131651835137, 1.3775597686645948, 'UPHENO:0004523', 'abnormal nervous system'),
(314166, 'HP:0025047', 'Abnormal brain choline level by MRS', 'XPO:0100734', 'abnormal lateral line system', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(314167, 'HP:0025047', 'Abnormal brain choline level by MRS', 'XPO:0100858', 'abnormal presumptive midbrain-hindbrain boundary', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(314168, 'HP:0025047', 'Abnormal brain choline level by MRS', 'XPO:0142051', 'abnormal cerebrospinal fluid', 0.43333333333333335, 3.94131651835137, 1.3068679445984308, 'UPHENO:0004523', 'abnormal nervous system'),
(314169, 'HP:0025047', 'Abnormal brain choline level by MRS', 'XPO:0100537', 'abnormal medium cavity', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(314170, 'HP:0025047', 'Abnormal brain choline level by MRS', 'XPO:0100164', 'abnormal neural nucleus', 0.43333333333333335, 3.94131651835137, 1.3068679445984308, 'UPHENO:0004523', 'abnormal nervous system'),
(314171, 'HP:0025047', 'Abnormal brain choline level by MRS', 'XPO:0100004', 'abnormal cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(314172, 'HP:0025047', 'Abnormal brain choline level by MRS', 'XPO:0101133', 'abnormal motor neuron', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(314173, 'HP:0025047', 'Abnormal brain choline level by MRS', 'XPO:0100864', 'abnormal dorsolateral ascending neuron', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(314174, 'HP:0025047', 'Abnormal brain choline level by MRS', 'XPO:0100702', 'abnormal glial cell', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(314175, 'HP:0025047', 'Abnormal brain choline level by MRS', 'XPO:0100916', 'abnormal principal cavity', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(314176, 'HP:0025047', 'Abnormal brain choline level by MRS', 'XPO:0100273', 'abnormal visual system', 0.4482758620689655, 3.94131651835137, 1.3292091859262085, 'UPHENO:0004523', 'abnormal nervous system'),
(314177, 'HP:0025047', 'Abnormal brain choline level by MRS', 'XPO:0100158', 'abnormal neuromere', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(314178, 'HP:0025047', 'Abnormal brain choline level by MRS', 'XPO:0100114', 'abnormal peripheral nervous system', 0.43333333333333335, 3.94131651835137, 1.3068679445984308, 'UPHENO:0004523', 'abnormal nervous system'),
(314179, 'HP:0025047', 'Abnormal brain choline level by MRS', 'XPO:0100031', 'abnormal central nervous system', 0.4642857142857143, 3.94131651835137, 1.3527368387638634, 'UPHENO:0004523', 'abnormal nervous system'),
(314180, 'HP:0025047', 'Abnormal brain choline level by MRS', 'XPO:0100175', 'abnormal migrating neuroblast', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(314181, 'HP:0025047', 'Abnormal brain choline level by MRS', 'XPO:0107253', 'abnormal enteric nervous system', 0.4642857142857143, 3.94131651835137, 1.3527368387638634, 'UPHENO:0004523', 'abnormal nervous system'),
(314182, 'HP:0025047', 'Abnormal brain choline level by MRS', 'XPO:0100196', 'abnormal neuron', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(314183, 'HP:0025047', 'Abnormal brain choline level by MRS', 'XPO:0100701', 'abnormal microglial cell', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(314184, 'HP:0025047', 'Abnormal brain choline level by MRS', 'XPO:0101501', 'abnormal parabrachial area', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(314185, 'HP:0025047', 'Abnormal brain choline level by MRS', 'XPO:0100760', 'abnormal Stirnorgan', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(314186, 'HP:0025047', 'Abnormal brain choline level by MRS', 'XPO:0101187', 'abnormal dorsolateral commissural neuron', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(314187, 'HP:0025047', 'Abnormal brain choline level by MRS', 'XPO:0100587', 'abnormal vestibuloauditory system', 0.4482758620689655, 3.94131651835137, 1.3292091859262085, 'UPHENO:0004523', 'abnormal nervous system'),
(314188, 'HP:0025047', 'Abnormal brain choline level by MRS', 'XPO:0100642', 'abnormal gustatory system', 0.4482758620689655, 3.94131651835137, 1.3292091859262085, 'UPHENO:0004523', 'abnormal nervous system'),
(314189, 'HP:0025047', 'Abnormal brain choline level by MRS', 'XPO:0100274', 'abnormal sensory system', 0.4642857142857143, 3.94131651835137, 1.3527368387638634, 'UPHENO:0004523', 'abnormal nervous system'),
(314190, 'HP:0025047', 'Abnormal brain choline level by MRS', 'XPO:0100954', 'abnormal neural progenitor cell', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(314191, 'HP:0025047', 'Abnormal brain choline level by MRS', 'XPO:0100427', 'abnormal olfactory system', 0.4482758620689655, 3.94131651835137, 1.3292091859262085, 'UPHENO:0004523', 'abnormal nervous system'),
(314192, 'HP:0006749', 'Malignant gastrointestinal tract tumors', 'XPO:0141612', 'metaplastic intestine', 0.40476190476190477, 7.4630184615845945, 1.7380292194851734, 'UPHENO:0002725', 'abnormal alimentary part of gastrointestinal system'),
(314193, 'HP:0006749', 'Malignant gastrointestinal tract tumors', 'XPO:0102522', 'abnormal pharyngeal cavity morphology', 0.4166666666666667, 5.05060299610679, 1.45066119926208, 'HP:0025031', 'Abnormality of the digestive system'),
(314194, 'HP:0006749', 'Malignant gastrointestinal tract tumors', 'XPO:0100006', 'abnormal anatomical structure', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(314195, 'HP:0006749', 'Malignant gastrointestinal tract tumors', 'XPO:0100572', 'abnormal branchial arch', 0.42857142857142855, 5.05060299610679, 1.471238981671103, 'HP:0025031', 'Abnormality of the digestive system'),
(314196, 'HP:0006749', 'Malignant gastrointestinal tract tumors', 'XPO:0100172', 'abnormal stem cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(314197, 'HP:0006749', 'Malignant gastrointestinal tract tumors', 'XPO:0115392', 'abnormally incomplete structure of alimentary system', 0.40540540540540543, 5.05060299610679, 1.4309233924911664, 'HP:0025031', 'Abnormality of the digestive system'),
(314198, 'HP:0006749', 'Malignant gastrointestinal tract tumors', 'XPO:0100454', 'abnormal lung bud', 0.42857142857142855, 5.05060299610679, 1.471238981671103, 'HP:0025031', 'Abnormality of the digestive system'),
(314199, 'HP:0006749', 'Malignant gastrointestinal tract tumors', 'XPO:0101004', 'abnormal acid secreting cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(314200, 'HP:0006749', 'Malignant gastrointestinal tract tumors', 'XPO:0100214', 'abnormal second pancreatic bud', 0.45454545454545453, 5.05060299610679, 1.5151662069205463, 'HP:0025031', 'Abnormality of the digestive system'),
(314201, 'HP:0006749', 'Malignant gastrointestinal tract tumors', 'XPO:0101169', 'abnormal hepato-pancreatic duct', 0.4838709677419355, 5.05060299610679, 1.5632786569919361, 'HP:0025031', 'Abnormality of the digestive system'),
(314202, 'HP:0006749', 'Malignant gastrointestinal tract tumors', 'XPO:0100494', 'abnormal liver diverticulum', 0.42857142857142855, 5.05060299610679, 1.471238981671103, 'HP:0025031', 'Abnormality of the digestive system'),
(314203, 'HP:0006749', 'Malignant gastrointestinal tract tumors', 'XPO:0101084', 'abnormal mesentery', 0.42857142857142855, 5.05060299610679, 1.471238981671103, 'HP:0025031', 'Abnormality of the digestive system'),
(314204, 'HP:0006749', 'Malignant gastrointestinal tract tumors', 'XPO:0101132', 'abnormal apoptotic cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(314205, 'HP:0006749', 'Malignant gastrointestinal tract tumors', 'XPO:0100130', 'abnormal mouth primordium', 0.4411764705882353, 5.05060299610679, 1.4927180591674907, 'HP:0025031', 'Abnormality of the digestive system'),
(314206, 'HP:0006749', 'Malignant gastrointestinal tract tumors', 'XPO:0101332', 'abnormal left spleen primordium', 0.4722222222222222, 7.4630184615845945, 1.877286116289935, 'UPHENO:0002725', 'abnormal alimentary part of gastrointestinal system'),
(314207, 'HP:0006749', 'Malignant gastrointestinal tract tumors', 'XPO:0100847', 'abnormal stomach', 0.4146341463414634, 7.4630184615845945, 1.7590970095335021, 'UPHENO:0002725', 'abnormal alimentary part of gastrointestinal system'),
(314208, 'HP:0006749', 'Malignant gastrointestinal tract tumors', 'XPO:0131683', 'abnormal stomach epithelium', 0.4411764705882353, 5.05060299610679, 1.4927180591674907, 'HP:0025031', 'Abnormality of the digestive system'),
(314209, 'HP:0006749', 'Malignant gastrointestinal tract tumors', 'XPO:0100481', 'abnormal anatomical line', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(314210, 'HP:0006749', 'Malignant gastrointestinal tract tumors', 'XPO:0101241', 'abnormal nucleate erythrocyte', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(314211, 'HP:0006749', 'Malignant gastrointestinal tract tumors', 'XPO:0100691', 'abnormal keratin accumulating cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(314212, 'HP:0006749', 'Malignant gastrointestinal tract tumors', 'XPO:0101103', 'abnormal pharyngeal mesenchyme', 0.42857142857142855, 5.05060299610679, 1.471238981671103, 'HP:0025031', 'Abnormality of the digestive system'),
(314213, 'HP:0006749', 'Malignant gastrointestinal tract tumors', 'XPO:0101373', 'abnormal oxygen accumulating cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(314214, 'HP:0006749', 'Malignant gastrointestinal tract tumors', 'XPO:0101101', 'abnormal posterior foregut', 0.5, 5.05060299610679, 1.5891197242666757, 'HP:0025031', 'Abnormality of the digestive system'),
(314215, 'HP:0006749', 'Malignant gastrointestinal tract tumors', 'XPO:0101297', 'abnormal barrier cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(314216, 'HP:0006749', 'Malignant gastrointestinal tract tumors', 'XPO:0142027', 'abnormally localised digestive tract', 0.40540540540540543, 5.05060299610679, 1.4309233924911664, 'HP:0025031', 'Abnormality of the digestive system'),
(314217, 'HP:0006749', 'Malignant gastrointestinal tract tumors', 'XPO:0101326', 'abnormal cementoblast', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(314218, 'HP:0006749', 'Malignant gastrointestinal tract tumors', 'XPO:0100216', 'abnormal hepato-pancreatic progenitor cell', 0.4411764705882353, 5.05060299610679, 1.4927180591674907, 'HP:0025031', 'Abnormality of the digestive system'),
(314219, 'HP:0006749', 'Malignant gastrointestinal tract tumors', 'XPO:0126499', 'abnormally localised liver and biliary system', 0.4166666666666667, 5.05060299610679, 1.45066119926208, 'HP:0025031', 'Abnormality of the digestive system'),
(314220, 'HP:0006749', 'Malignant gastrointestinal tract tumors', 'XPO:0124857', 'absent alimentary system', 0.4166666666666667, 5.05060299610679, 1.45066119926208, 'HP:0025031', 'Abnormality of the digestive system'),
(314221, 'HP:0006749', 'Malignant gastrointestinal tract tumors', 'XPO:0126466', 'abnormally localised alimentary system', 0.42857142857142855, 5.05060299610679, 1.471238981671103, 'HP:0025031', 'Abnormality of the digestive system'),
(314222, 'HP:0006749', 'Malignant gastrointestinal tract tumors', 'XPO:0107307', 'abnormal posterior hindgut endoderm', 0.45454545454545453, 5.05060299610679, 1.5151662069205463, 'HP:0025031', 'Abnormality of the digestive system'),
(314223, 'HP:0006749', 'Malignant gastrointestinal tract tumors', 'XPO:0100477', 'abnormal pericyte', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(314224, 'HP:0006749', 'Malignant gastrointestinal tract tumors', 'XPO:0126837', 'abnormally localised midgut', 0.40540540540540543, 5.05060299610679, 1.4309233924911664, 'HP:0025031', 'Abnormality of the digestive system'),
(314225, 'HP:0006749', 'Malignant gastrointestinal tract tumors', 'XPO:0101021', 'abnormal dorsal foregut', 0.5, 5.05060299610679, 1.5891197242666757, 'HP:0025031', 'Abnormality of the digestive system'),
(314226, 'HP:0006749', 'Malignant gastrointestinal tract tumors', 'XPO:0107304', 'abnormal hindgut endoderm', 0.46875, 5.05060299610679, 1.5386585568036393, 'HP:0025031', 'Abnormality of the digestive system'),
(314227, 'HP:0006749', 'Malignant gastrointestinal tract tumors', 'XPO:0100492', 'abnormal gall bladder primordium', 0.46875, 5.05060299610679, 1.5386585568036393, 'HP:0025031', 'Abnormality of the digestive system'),
(314228, 'HP:0006749', 'Malignant gastrointestinal tract tumors', 'XPO:0100986', 'abnormal gut epithelium', 0.5, 5.05060299610679, 1.5891197242666757, 'HP:0025031', 'Abnormality of the digestive system'),
(314229, 'HP:0006749', 'Malignant gastrointestinal tract tumors', 'XPO:0142054', 'abnormal digestive tract', 0.5357142857142857, 5.05060299610679, 1.6448951870820767, 'HP:0025031', 'Abnormality of the digestive system'),
(314230, 'HP:0006749', 'Malignant gastrointestinal tract tumors', 'XPO:0100004', 'abnormal cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(314231, 'HP:0006749', 'Malignant gastrointestinal tract tumors', 'XPO:0101435', 'abnormal paracrine cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(314232, 'HP:0006749', 'Malignant gastrointestinal tract tumors', 'XPO:0101156', 'abnormal typhlosole', 0.425, 7.4630184615845945, 1.7809499841863758, 'UPHENO:0002725', 'abnormal alimentary part of gastrointestinal system'),
(314233, 'HP:0006749', 'Malignant gastrointestinal tract tumors', 'XPO:0100621', 'abnormal peritoneum', 0.46875, 5.05060299610679, 1.5386585568036393, 'HP:0025031', 'Abnormality of the digestive system'),
(314234, 'HP:0006749', 'Malignant gastrointestinal tract tumors', 'XPO:0100026', 'abnormal germ cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(314235, 'HP:0006749', 'Malignant gastrointestinal tract tumors', 'XPO:0100662', 'abnormal lung primordium', 0.40540540540540543, 5.05060299610679, 1.4309233924911664, 'HP:0025031', 'Abnormality of the digestive system'),
(314236, 'HP:0006749', 'Malignant gastrointestinal tract tumors', 'XPO:0115391', 'abnormally undifferentiated alimentary system', 0.5555555555555556, 5.05060299610679, 1.6750792677938144, 'HP:0025031', 'Abnormality of the digestive system'),
(314237, 'HP:0006749', 'Malignant gastrointestinal tract tumors', 'XPO:0100344', 'abnormal portion of organism substance', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(314238, 'HP:0006749', 'Malignant gastrointestinal tract tumors', 'XPO:0101198', 'abnormal digestive enzyme secreting cell', 0.46875, 5.05060299610679, 1.5386585568036393, 'HP:0025031', 'Abnormality of the digestive system'),
(314239, 'HP:0006749', 'Malignant gastrointestinal tract tumors', 'XPO:0100890', 'abnormal pharyngeal cavity', 0.5357142857142857, 5.05060299610679, 1.6448951870820767, 'HP:0025031', 'Abnormality of the digestive system'),
(314240, 'HP:0006749', 'Malignant gastrointestinal tract tumors', 'XPO:0141717', 'abnormal tracheoesophageal fold', 0.45454545454545453, 5.05060299610679, 1.5151662069205463, 'HP:0025031', 'Abnormality of the digestive system'),
(314241, 'HP:0006749', 'Malignant gastrointestinal tract tumors', 'XPO:0101381', 'abnormal ventral foregut', 0.5, 5.05060299610679, 1.5891197242666757, 'HP:0025031', 'Abnormality of the digestive system'),
(314242, 'HP:0006749', 'Malignant gastrointestinal tract tumors', 'XPO:0100629', 'abnormal branchial arch 2', 0.4166666666666667, 5.05060299610679, 1.45066119926208, 'HP:0025031', 'Abnormality of the digestive system'),
(314243, 'HP:0006749', 'Malignant gastrointestinal tract tumors', 'XPO:0127393', 'abnormally localised pharyngeal cavity', 0.42857142857142855, 5.05060299610679, 1.471238981671103, 'HP:0025031', 'Abnormality of the digestive system'),
(314244, 'HP:0006749', 'Malignant gastrointestinal tract tumors', 'XPO:0101784', 'abnormal alimentary system morphology', 0.4166666666666667, 5.05060299610679, 1.45066119926208, 'HP:0025031', 'Abnormality of the digestive system'),
(314245, 'HP:0006749', 'Malignant gastrointestinal tract tumors', 'XPO:0100188', 'abnormal delta cell', 0.42857142857142855, 5.05060299610679, 1.471238981671103, 'HP:0025031', 'Abnormality of the digestive system'),
(314246, 'HP:0006749', 'Malignant gastrointestinal tract tumors', 'XPO:0100523', 'abnormal midgut', 0.5172413793103449, 5.05060299610679, 1.6162861318637973, 'HP:0025031', 'Abnormality of the digestive system'),
(314247, 'HP:0006749', 'Malignant gastrointestinal tract tumors', 'XPO:0101237', 'abnormal mucus secreting cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(314248, 'HP:0006749', 'Malignant gastrointestinal tract tumors', 'XPO:0100704', 'abnormal Merkel cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(314249, 'HP:0006749', 'Malignant gastrointestinal tract tumors', 'XPO:0126705', 'abnormally localised larval alimentary system', 0.40540540540540543, 5.05060299610679, 1.4309233924911664, 'HP:0025031', 'Abnormality of the digestive system'),
(314250, 'HP:0006749', 'Malignant gastrointestinal tract tumors', 'XPO:0100715', 'abnormal ciliated cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(314251, 'HP:0006749', 'Malignant gastrointestinal tract tumors', 'XPO:0100156', 'abnormal foregut', 0.5172413793103449, 5.05060299610679, 1.6162861318637973, 'HP:0025031', 'Abnormality of the digestive system'),
(314252, 'HP:0006749', 'Malignant gastrointestinal tract tumors', 'XPO:0100797', 'abnormal esophagus', 0.4166666666666667, 5.05060299610679, 1.45066119926208, 'HP:0025031', 'Abnormality of the digestive system'),
(314253, 'HP:0006749', 'Malignant gastrointestinal tract tumors', 'XPO:0101377', 'abnormal manicotto glandulare', 0.5172413793103449, 5.05060299610679, 1.6162861318637973, 'HP:0025031', 'Abnormality of the digestive system'),
(314254, 'HP:0006749', 'Malignant gastrointestinal tract tumors', 'XPO:0100152', 'abnormal alimentary system', 0.5769230769230769, 5.05060299610679, 1.706988406765213, 'HP:0025031', 'Abnormality of the digestive system'),
(314255, 'HP:0006749', 'Malignant gastrointestinal tract tumors', 'XPO:0100735', 'abnormal hindgut', 0.5172413793103449, 5.05060299610679, 1.6162861318637973, 'HP:0025031', 'Abnormality of the digestive system'),
(314256, 'HP:0006749', 'Malignant gastrointestinal tract tumors', 'XPO:0100571', 'abnormal branchial arch 1', 0.4166666666666667, 5.05060299610679, 1.45066119926208, 'HP:0025031', 'Abnormality of the digestive system'),
(314257, 'HP:0006749', 'Malignant gastrointestinal tract tumors', 'XPO:0127307', 'abnormally localised oral evagination', 0.40540540540540543, 5.05060299610679, 1.4309233924911664, 'HP:0025031', 'Abnormality of the digestive system'),
(314258, 'HP:0006749', 'Malignant gastrointestinal tract tumors', 'XPO:0125745', 'absent pharyngeal cavity', 0.4166666666666667, 5.05060299610679, 1.45066119926208, 'HP:0025031', 'Abnormality of the digestive system'),
(314259, 'HP:0006749', 'Malignant gastrointestinal tract tumors', 'XPO:0115495', 'abnormally protruding proctodeum', 0.4411764705882353, 5.05060299610679, 1.4927180591674907, 'HP:0025031', 'Abnormality of the digestive system'),
(314260, 'HP:0006749', 'Malignant gastrointestinal tract tumors', 'XPO:0100771', 'abnormal distal stomach', 0.40476190476190477, 7.4630184615845945, 1.7380292194851734, 'UPHENO:0002725', 'abnormal alimentary part of gastrointestinal system'),
(314261, 'HP:0006749', 'Malignant gastrointestinal tract tumors', 'XPO:0101467', 'abnormal alkali secreting cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(314262, 'HP:0006749', 'Malignant gastrointestinal tract tumors', 'XPO:0100591', 'abnormal pharyngeal arch', 0.4411764705882353, 5.05060299610679, 1.4927180591674907, 'HP:0025031', 'Abnormality of the digestive system'),
(314263, 'HP:0006749', 'Malignant gastrointestinal tract tumors', 'XPO:0101535', 'abnormal absorptive cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(314264, 'HP:0006749', 'Malignant gastrointestinal tract tumors', 'XPO:0100718', 'abnormal ventral pancreatic bud', 0.4838709677419355, 5.05060299610679, 1.5632786569919361, 'HP:0025031', 'Abnormality of the digestive system'),
(314265, 'HP:0006749', 'Malignant gastrointestinal tract tumors', 'XPO:0100391', 'abnormal proximal stomach', 0.40476190476190477, 7.4630184615845945, 1.7380292194851734, 'UPHENO:0002725', 'abnormal alimentary part of gastrointestinal system'),
(314266, 'HP:0006749', 'Malignant gastrointestinal tract tumors', 'XPO:0124888', 'absent liver and biliary system', 0.40540540540540543, 5.05060299610679, 1.4309233924911664, 'HP:0025031', 'Abnormality of the digestive system'),
(314267, 'HP:0006749', 'Malignant gastrointestinal tract tumors', 'XPO:0100813', 'abnormal branchial arch 3', 0.4166666666666667, 5.05060299610679, 1.45066119926208, 'HP:0025031', 'Abnormality of the digestive system'),
(314268, 'HP:0006749', 'Malignant gastrointestinal tract tumors', 'XPO:0100638', 'abnormal polar body', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(314269, 'HP:0006749', 'Malignant gastrointestinal tract tumors', 'XPO:0100462', 'abnormal anterior foregut', 0.5, 5.05060299610679, 1.5891197242666757, 'HP:0025031', 'Abnormality of the digestive system'),
(314270, 'HP:0006749', 'Malignant gastrointestinal tract tumors', 'XPO:0101601', 'abnormal proctodeum', 0.4838709677419355, 5.05060299610679, 1.5632786569919361, 'HP:0025031', 'Abnormality of the digestive system'),
(314271, 'HP:0006749', 'Malignant gastrointestinal tract tumors', 'XPO:0100788', 'abnormal branchial arch 4', 0.4166666666666667, 5.05060299610679, 1.45066119926208, 'HP:0025031', 'Abnormality of the digestive system'),
(314272, 'HP:0006749', 'Malignant gastrointestinal tract tumors', 'XPO:0100802', 'abnormal exocrine cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(314273, 'HP:0006749', 'Malignant gastrointestinal tract tumors', 'XPO:0100486', 'abnormal oral evagination', 0.5172413793103449, 5.05060299610679, 1.6162861318637973, 'HP:0025031', 'Abnormality of the digestive system'),
(314274, 'HP:0006749', 'Malignant gastrointestinal tract tumors', 'XPO:0100549', 'abnormal mitotic cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(314275, 'HP:0006749', 'Malignant gastrointestinal tract tumors', 'XPO:0100108', 'abnormal cell part', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(314276, 'HP:0006749', 'Malignant gastrointestinal tract tumors', 'XPO:0107305', 'abnormal dorsal posterior hindgut endoderm', 0.4411764705882353, 5.05060299610679, 1.4927180591674907, 'HP:0025031', 'Abnormality of the digestive system'),
(314277, 'HP:0006749', 'Malignant gastrointestinal tract tumors', 'XPO:0100791', 'abnormal multiciliated cell precursor', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(314278, 'HP:0006749', 'Malignant gastrointestinal tract tumors', 'XPO:0100852', 'abnormal interdigital region', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(314279, 'HP:0006749', 'Malignant gastrointestinal tract tumors', 'XPO:0100289', 'abnormal chondroblast', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(314280, 'HP:0006749', 'Malignant gastrointestinal tract tumors', 'XPO:0100841', 'abnormal large intestine', 0.4358974358974359, 7.4630184615845945, 1.8036381597925764, 'UPHENO:0002725', 'abnormal alimentary part of gastrointestinal system'),
(314281, 'HP:0006749', 'Malignant gastrointestinal tract tumors', 'XPO:0100653', 'abnormal myoblast', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(314282, 'HP:0006749', 'Malignant gastrointestinal tract tumors', 'XPO:0126520', 'abnormally localised hindgut', 0.40540540540540543, 5.05060299610679, 1.4309233924911664, 'HP:0025031', 'Abnormality of the digestive system'),
(314283, 'HP:0006749', 'Malignant gastrointestinal tract tumors', 'XPO:0107308', 'abnormal anterior hindgut endoderm', 0.45454545454545453, 5.05060299610679, 1.5151662069205463, 'HP:0025031', 'Abnormality of the digestive system'),
(314284, 'HP:0006749', 'Malignant gastrointestinal tract tumors', 'XPO:0100754', 'abnormal electrically active cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(314285, 'HP:0006749', 'Malignant gastrointestinal tract tumors', 'XPO:0100337', 'abnormal zygote', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(314286, 'HP:0006749', 'Malignant gastrointestinal tract tumors', 'XPO:0126608', 'abnormally localised foregut', 0.40540540540540543, 5.05060299610679, 1.4309233924911664, 'HP:0025031', 'Abnormality of the digestive system'),
(314287, 'HP:0006749', 'Malignant gastrointestinal tract tumors', 'XPO:0100903', 'abnormal dorsal pancreatic bud', 0.4166666666666667, 5.05060299610679, 1.45066119926208, 'HP:0025031', 'Abnormality of the digestive system'),
(314288, 'HP:0006749', 'Malignant gastrointestinal tract tumors', 'XPO:0131662', 'abnormal foregut epithelium', 0.4411764705882353, 5.05060299610679, 1.4927180591674907, 'HP:0025031', 'Abnormality of the digestive system'),
(314289, 'HP:0006749', 'Malignant gastrointestinal tract tumors', 'XPO:0100081', 'abnormal anatomical entity in vitro', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(314290, 'HP:0006749', 'Malignant gastrointestinal tract tumors', 'XPO:0101333', 'abnormal barrier epithelial cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(314291, 'HP:0006749', 'Malignant gastrointestinal tract tumors', 'XPO:0100524', 'abnormal intestine', 0.4473684210526316, 7.4630184615845945, 1.8272161299216192, 'UPHENO:0002725', 'abnormal alimentary part of gastrointestinal system'),
(314292, 'HP:0006749', 'Malignant gastrointestinal tract tumors', 'XPO:0107288', 'abnormal larval alimentary system', 0.5555555555555556, 5.05060299610679, 1.6750792677938144, 'HP:0025031', 'Abnormality of the digestive system'),
(314293, 'HP:0006749', 'Malignant gastrointestinal tract tumors', 'XPO:0107306', 'abnormal ventral posterior hindgut endoderm', 0.4411764705882353, 5.05060299610679, 1.4927180591674907, 'HP:0025031', 'Abnormality of the digestive system'),
(314294, 'HP:0006749', 'Malignant gastrointestinal tract tumors', 'XPO:0100533', 'abnormal melanoblast', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(314295, 'HP:0006749', 'Malignant gastrointestinal tract tumors', 'XPO:0100493', 'abnormal liver and biliary system', 0.5555555555555556, 5.05060299610679, 1.6750792677938144, 'HP:0025031', 'Abnormality of the digestive system'),
(314296, 'HP:0006749', 'Malignant gastrointestinal tract tumors', 'XPO:0101309', 'abnormal colon', 0.425, 7.4630184615845945, 1.7809499841863758, 'UPHENO:0002725', 'abnormal alimentary part of gastrointestinal system'),
(314297, 'HP:0006749', 'Malignant gastrointestinal tract tumors', 'XPO:0131673', 'abnormal buccopharyngeal membrane', 0.42857142857142855, 5.05060299610679, 1.471238981671103, 'HP:0025031', 'Abnormality of the digestive system'),
(314298, 'HP:0006749', 'Malignant gastrointestinal tract tumors', 'XPO:0101448', 'abnormal myelin accumulating cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(314299, 'HP:0006749', 'Malignant gastrointestinal tract tumors', 'XPO:0100893', 'abnormal hyoid arch', 0.42857142857142855, 5.05060299610679, 1.471238981671103, 'HP:0025031', 'Abnormality of the digestive system'),
(314300, 'HP:0006749', 'Malignant gastrointestinal tract tumors', 'XPO:0100215', 'abnormal first pancreatic bud', 0.46875, 5.05060299610679, 1.5386585568036393, 'HP:0025031', 'Abnormality of the digestive system'),
(314301, 'HP:0006749', 'Malignant gastrointestinal tract tumors', 'XPO:0100285', 'abnormal progenitor cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(314302, 'HP:0012220', 'Non-caseating epithelioid cell granulomatosis', 'XPO:0102965', 'abnormal barrier epithelial cell morphology', 0.41304347826086957, 5.43643956286526, 1.4984945466703803, 'HP:0025461', 'Abnormal cell morphology'),
(314303, 'HP:0012220', 'Non-caseating epithelioid cell granulomatosis', 'XPO:0102739', 'abnormal erythroid cell morphology', 0.42, 5.574066539846944, 1.5300679549404714, 'HP:0001871', 'Abnormality of blood and blood-forming tissues'),
(314304, 'HP:0012220', 'Non-caseating epithelioid cell granulomatosis', 'XPO:0102165', 'abnormal melanoblast morphology', 0.41304347826086957, 5.43643956286526, 1.4984945466703803, 'HP:0025461', 'Abnormal cell morphology'),
(314305, 'HP:0012220', 'Non-caseating epithelioid cell granulomatosis', 'XPO:0102347', 'abnormal ciliated cell morphology', 0.41304347826086957, 5.43643956286526, 1.4984945466703803, 'HP:0025461', 'Abnormal cell morphology'),
(314306, 'HP:0012220', 'Non-caseating epithelioid cell granulomatosis', 'XPO:0102958', 'abnormal cementoblast morphology', 0.41304347826086957, 5.43643956286526, 1.4984945466703803, 'HP:0025461', 'Abnormal cell morphology'),
(314307, 'HP:0012220', 'Non-caseating epithelioid cell granulomatosis', 'XPO:0102715', 'abnormal T cell morphology', 0.43137254901960786, 6.786309419308587, 1.7109727036522004, 'UPHENO:0087123', 'abnormal immune system morphology'),
(314308, 'HP:0012220', 'Non-caseating epithelioid cell granulomatosis', 'XPO:0102929', 'abnormal barrier cell morphology', 0.41304347826086957, 5.43643956286526, 1.4984945466703803, 'HP:0025461', 'Abnormal cell morphology'),
(314309, 'HP:0012220', 'Non-caseating epithelioid cell granulomatosis', 'XPO:0102081', 'abnormal lymphocyte morphology', 0.4489795918367347, 6.786309419308587, 1.7455413009032348, 'UPHENO:0087123', 'abnormal immune system morphology'),
(314310, 'HP:0012220', 'Non-caseating epithelioid cell granulomatosis', 'XPO:0102873', 'abnormal nucleate erythrocyte morphology', 0.41304347826086957, 5.43643956286526, 1.4984945466703803, 'HP:0025461', 'Abnormal cell morphology'),
(314311, 'HP:0012220', 'Non-caseating epithelioid cell granulomatosis', 'XPO:0103067', 'abnormal paracrine cell morphology', 0.41304347826086957, 5.43643956286526, 1.4984945466703803, 'HP:0025461', 'Abnormal cell morphology'),
(314312, 'HP:0012220', 'Non-caseating epithelioid cell granulomatosis', 'XPO:0103082', 'abnormal myeloid cell morphology', 0.42, 5.574066539846944, 1.5300679549404714, 'UPHENO:0004459', 'abnormal hematopoietic system'),
(314313, 'HP:0012220', 'Non-caseating epithelioid cell granulomatosis', 'XPO:0103219', 'abnormal hemangioblast morphology', 0.42, 5.574066539846944, 1.5300679549404714, 'UPHENO:0004459', 'abnormal hematopoietic system'),
(314314, 'HP:0012220', 'Non-caseating epithelioid cell granulomatosis', 'XPO:0102764', 'abnormal apoptotic cell morphology', 0.41304347826086957, 5.43643956286526, 1.4984945466703803, 'HP:0025461', 'Abnormal cell morphology'),
(314315, 'HP:0012220', 'Non-caseating epithelioid cell granulomatosis', 'XPO:0103150', 'abnormal B cell morphology', 0.43137254901960786, 6.786309419308587, 1.7109727036522004, 'UPHENO:0087123', 'abnormal immune system morphology'),
(314316, 'HP:0012220', 'Non-caseating epithelioid cell granulomatosis', 'XPO:0102423', 'abnormal multiciliated cell precursor morphology', 0.41304347826086957, 5.43643956286526, 1.4984945466703803, 'HP:0025461', 'Abnormal cell morphology'),
(314317, 'HP:0012220', 'Non-caseating epithelioid cell granulomatosis', 'XPO:0101658', 'abnormal germ cell morphology', 0.41304347826086957, 5.43643956286526, 1.4984945466703803, 'HP:0025461', 'Abnormal cell morphology'),
(314318, 'HP:0012220', 'Non-caseating epithelioid cell granulomatosis', 'XPO:0101804', 'abnormal stem cell morphology', 0.41304347826086957, 5.43643956286526, 1.4984945466703803, 'HP:0025461', 'Abnormal cell morphology'),
(314319, 'HP:0012220', 'Non-caseating epithelioid cell granulomatosis', 'XPO:0139717', 'abnormally necrotic cell', 0.40425531914893614, 5.43643956286526, 1.4824674062251753, 'HP:0025461', 'Abnormal cell morphology'),
(314320, 'HP:0012220', 'Non-caseating epithelioid cell granulomatosis', 'XPO:0101969', 'abnormal zygote morphology', 0.41304347826086957, 5.43643956286526, 1.4984945466703803, 'HP:0025461', 'Abnormal cell morphology'),
(314321, 'HP:0012220', 'Non-caseating epithelioid cell granulomatosis', 'XPO:0102109', 'abnormal pericyte morphology', 0.41304347826086957, 5.43643956286526, 1.4984945466703803, 'HP:0025461', 'Abnormal cell morphology'),
(314322, 'HP:0012220', 'Non-caseating epithelioid cell granulomatosis', 'XPO:0103005', 'abnormal oxygen accumulating cell morphology', 0.41304347826086957, 5.43643956286526, 1.4984945466703803, 'HP:0025461', 'Abnormal cell morphology'),
(314323, 'HP:0012220', 'Non-caseating epithelioid cell granulomatosis', 'XPO:0141478', 'abnormally necrotic lymphoblast', 0.41509433962264153, 6.786309419308587, 1.6783797624145764, 'UPHENO:0087123', 'abnormal immune system morphology'),
(314324, 'HP:0012220', 'Non-caseating epithelioid cell granulomatosis', 'XPO:0103167', 'abnormal absorptive cell morphology', 0.41304347826086957, 5.43643956286526, 1.4984945466703803, 'HP:0025461', 'Abnormal cell morphology'),
(314325, 'HP:0012220', 'Non-caseating epithelioid cell granulomatosis', 'XPO:0139951', 'abnormally necrotic lymphocyte', 0.41509433962264153, 6.786309419308587, 1.6783797624145764, 'UPHENO:0087123', 'abnormal immune system morphology'),
(314326, 'HP:0012220', 'Non-caseating epithelioid cell granulomatosis', 'XPO:0102323', 'abnormal keratin accumulating cell morphology', 0.41304347826086957, 5.43643956286526, 1.4984945466703803, 'HP:0025461', 'Abnormal cell morphology'),
(314327, 'HP:0012220', 'Non-caseating epithelioid cell granulomatosis', 'XPO:0101917', 'abnormal progenitor cell morphology', 0.41304347826086957, 5.43643956286526, 1.4984945466703803, 'HP:0025461', 'Abnormal cell morphology'),
(314328, 'HP:0012220', 'Non-caseating epithelioid cell granulomatosis', 'XPO:0102336', 'abnormal Merkel cell morphology', 0.41304347826086957, 5.43643956286526, 1.4984945466703803, 'HP:0025461', 'Abnormal cell morphology'),
(314329, 'HP:0012220', 'Non-caseating epithelioid cell granulomatosis', 'XPO:0102434', 'abnormal exocrine cell morphology', 0.41304347826086957, 5.43643956286526, 1.4984945466703803, 'HP:0025461', 'Abnormal cell morphology'),
(314330, 'HP:0012220', 'Non-caseating epithelioid cell granulomatosis', 'XPO:0101921', 'abnormal chondroblast morphology', 0.41304347826086957, 5.43643956286526, 1.4984945466703803, 'HP:0025461', 'Abnormal cell morphology'),
(314331, 'HP:0012220', 'Non-caseating epithelioid cell granulomatosis', 'XPO:0101636', 'abnormal cell morphology', 0.4318181818181818, 5.43643956286526, 1.532172786470543, 'HP:0025461', 'Abnormal cell morphology'),
(314332, 'HP:0012220', 'Non-caseating epithelioid cell granulomatosis', 'XPO:0141503', 'abnormal lymphoblast morphology', 0.4489795918367347, 6.786309419308587, 1.7455413009032348, 'UPHENO:0087123', 'abnormal immune system morphology'),
(314333, 'HP:0012220', 'Non-caseating epithelioid cell granulomatosis', 'XPO:0103080', 'abnormal myelin accumulating cell morphology', 0.41304347826086957, 5.43643956286526, 1.4984945466703803, 'HP:0025461', 'Abnormal cell morphology'),
(314334, 'HP:0012220', 'Non-caseating epithelioid cell granulomatosis', 'XPO:0102181', 'abnormal mitotic cell morphology', 0.41304347826086957, 5.43643956286526, 1.4984945466703803, 'HP:0025461', 'Abnormal cell morphology'),
(314335, 'HP:0012220', 'Non-caseating epithelioid cell granulomatosis', 'XPO:0102285', 'abnormal myoblast morphology', 0.41304347826086957, 5.43643956286526, 1.4984945466703803, 'HP:0025461', 'Abnormal cell morphology'),
(314336, 'HP:0012220', 'Non-caseating epithelioid cell granulomatosis', 'XPO:0102446', 'abnormal natural killer cell morphology', 0.41509433962264153, 6.786309419308587, 1.6783797624145764, 'UPHENO:0087123', 'abnormal immune system morphology'),
(314337, 'HP:0012220', 'Non-caseating epithelioid cell granulomatosis', 'XPO:0102869', 'abnormal mucus secreting cell morphology', 0.41304347826086957, 5.43643956286526, 1.4984945466703803, 'HP:0025461', 'Abnormal cell morphology'),
(314338, 'HP:0012220', 'Non-caseating epithelioid cell granulomatosis', 'XPO:0103099', 'abnormal alkali secreting cell morphology', 0.41304347826086957, 5.43643956286526, 1.4984945466703803, 'HP:0025461', 'Abnormal cell morphology'),
(314339, 'HP:0012220', 'Non-caseating epithelioid cell granulomatosis', 'XPO:0102636', 'abnormal acid secreting cell morphology', 0.41304347826086957, 5.43643956286526, 1.4984945466703803, 'HP:0025461', 'Abnormal cell morphology'),
(314340, 'HP:0012220', 'Non-caseating epithelioid cell granulomatosis', 'XPO:0102386', 'abnormal electrically active cell morphology', 0.41304347826086957, 5.43643956286526, 1.4984945466703803, 'HP:0025461', 'Abnormal cell morphology'),
(314341, 'HP:0034936', 'Elevated circulating lathosterol concentration', 'XPO:0141873', 'abnormal tricarboxylic acid metabolic process', 0.4107142857142857, 7.41682187759612, 1.745335125334667, 'HP:0430071', 'Abnormal circulating organic compound concentration'),
(314342, 'HP:0004309', 'Ventricular preexcitation', 'XPO:0100054', 'abnormal blood vessel', 0.4117647058823529, 5.249153838287537, 1.4701755971154233, 'UPHENO:0080362', 'abnormal cardiovascular system'),
(314343, 'HP:0011153', 'Focal motor seizure', 'XPO:0100587', 'abnormal vestibuloauditory system', 0.43333333333333335, 3.94131651835137, 1.3068679445984308, 'UPHENO:0004523', 'abnormal nervous system'),
(314344, 'HP:0011153', 'Focal motor seizure', 'XPO:0100273', 'abnormal visual system', 0.43333333333333335, 3.94131651835137, 1.3068679445984308, 'UPHENO:0004523', 'abnormal nervous system'),
(314345, 'HP:0011153', 'Focal motor seizure', 'XPO:0100032', 'abnormal nervous system', 0.4642857142857143, 3.94131651835137, 1.3527368387638634, 'UPHENO:0004523', 'abnormal nervous system'),
(314346, 'HP:0011153', 'Focal motor seizure', 'XPO:0100642', 'abnormal gustatory system', 0.43333333333333335, 3.94131651835137, 1.3068679445984308, 'UPHENO:0004523', 'abnormal nervous system'),
(314347, 'HP:0011153', 'Focal motor seizure', 'XPO:0100164', 'abnormal neural nucleus', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(314348, 'HP:0011153', 'Focal motor seizure', 'XPO:0100158', 'abnormal neuromere', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(314349, 'HP:0011153', 'Focal motor seizure', 'XPO:0100196', 'abnormal neuron', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(314350, 'HP:0011153', 'Focal motor seizure', 'XPO:0100702', 'abnormal glial cell', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(314351, 'HP:0011153', 'Focal motor seizure', 'XPO:0100274', 'abnormal sensory system', 0.4482758620689655, 3.94131651835137, 1.3292091859262085, 'UPHENO:0004523', 'abnormal nervous system'),
(314352, 'HP:0011153', 'Focal motor seizure', 'XPO:0107253', 'abnormal enteric nervous system', 0.4482758620689655, 3.94131651835137, 1.3292091859262085, 'UPHENO:0004523', 'abnormal nervous system'),
(314353, 'HP:0011153', 'Focal motor seizure', 'XPO:0100175', 'abnormal migrating neuroblast', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(314354, 'HP:0011153', 'Focal motor seizure', 'XPO:0101501', 'abnormal parabrachial area', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(314355, 'HP:0011153', 'Focal motor seizure', 'XPO:0100858', 'abnormal presumptive midbrain-hindbrain boundary', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(314356, 'HP:0011153', 'Focal motor seizure', 'XPO:0100916', 'abnormal principal cavity', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(314357, 'HP:0011153', 'Focal motor seizure', 'XPO:0100031', 'abnormal central nervous system', 0.4482758620689655, 3.94131651835137, 1.3292091859262085, 'UPHENO:0004523', 'abnormal nervous system'),
(314358, 'HP:0011153', 'Focal motor seizure', 'XPO:0100537', 'abnormal medium cavity', 0.40625, 3.94131651835137, 1.2653694462805098, 'UPHENO:0004523', 'abnormal nervous system'),
(314359, 'HP:0011153', 'Focal motor seizure', 'XPO:0100427', 'abnormal olfactory system', 0.43333333333333335, 3.94131651835137, 1.3068679445984308, 'UPHENO:0004523', 'abnormal nervous system'),
(314360, 'HP:0011153', 'Focal motor seizure', 'XPO:0100114', 'abnormal peripheral nervous system', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(314361, 'HP:0011153', 'Focal motor seizure', 'XPO:0142051', 'abnormal cerebrospinal fluid', 0.41935483870967744, 3.94131651835137, 1.2856166430382838, 'UPHENO:0004523', 'abnormal nervous system'),
(314362, 'HP:0012769', 'Abnormal arm span', 'XPO:0141787', 'abnormal hormone metabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(314363, 'HP:0012769', 'Abnormal arm span', 'XPO:0100610', 'abnormal appendage', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(314364, 'HP:0012769', 'Abnormal arm span', 'XPO:0100084', 'abnormal anatomical group', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(314365, 'HP:0012769', 'Abnormal arm span', 'XPO:0100846', 'abnormal hindlimb', 0.5, 5.504475013697824, 1.6589868917049684, 'HP:0040064', 'Abnormality of limbs'),
(314366, 'HP:0012769', 'Abnormal arm span', 'XPO:0100268', 'abnormal circulatory system', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(314367, 'HP:0012769', 'Abnormal arm span', 'XPO:0101221', 'abnormal larval immune system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(314368, 'HP:0012769', 'Abnormal arm span', 'XPO:0141783', 'abnormal collagen metabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(314369, 'HP:0012769', 'Abnormal arm span', 'XPO:0100344', 'abnormal portion of organism substance', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(314370, 'HP:0012769', 'Abnormal arm span', 'XPO:0100626', 'abnormal primordial germ cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(314371, 'HP:0012769', 'Abnormal arm span', 'XPO:0100062', 'abnormal anatomical space', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(314372, 'HP:0012769', 'Abnormal arm span', 'XPO:0100289', 'abnormal chondroblast', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(314373, 'HP:0012769', 'Abnormal arm span', 'XPO:0101406', 'abnormal cleavage furrow', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(314374, 'HP:0012769', 'Abnormal arm span', 'XPO:0141786', 'abnormal pigment metabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(314375, 'HP:0012769', 'Abnormal arm span', 'XPO:0100807', 'abnormal matrix-based tissue', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(314376, 'HP:0012769', 'Abnormal arm span', 'XPO:0131687', 'abnormal astral microtubule', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(314377, 'HP:0012769', 'Abnormal arm span', 'XPO:0100205', 'abnormal limb segment', 0.5416666666666666, 5.504475013697824, 1.7267283030111178, 'HP:0040064', 'Abnormality of limbs'),
(314378, 'HP:0012769', 'Abnormal arm span', 'XPO:0141499', 'abnormal tadpole', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(314379, 'HP:0012769', 'Abnormal arm span', 'XPO:0107258', 'abnormal anatomical axis', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(314380, 'HP:0012769', 'Abnormal arm span', 'XPO:0141663', 'paralysed hindlimb', 0.43333333333333335, 5.504475013697824, 1.5444327456822857, 'HP:0040064', 'Abnormality of limbs'),
(314381, 'HP:0012769', 'Abnormal arm span', 'XPO:0100745', 'abnormal anterior lymph sac', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(314382, 'HP:0012769', 'Abnormal arm span', 'XPO:0101535', 'abnormal absorptive cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(314383, 'HP:0012769', 'Abnormal arm span', 'XPO:0101228', 'abnormal mesenchymal stem cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(314384, 'HP:0012769', 'Abnormal arm span', 'XPO:0125566', 'absent interdigital region', 0.41935483870967744, 5.504475013697824, 1.5193183443737854, 'HP:0040064', 'Abnormality of limbs'),
(314385, 'HP:0012769', 'Abnormal arm span', 'XPO:0100003', 'abnormal organism subdivision', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(314386, 'HP:0012769', 'Abnormal arm span', 'XPO:0101096', 'abnormal tendon', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(314387, 'HP:0012769', 'Abnormal arm span', 'XPO:0141775', 'abnormal nitrogen compound metabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(314388, 'HP:0012769', 'Abnormal arm span', 'XPO:0100786', 'abnormal presumptive axial mesoderm', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(314389, 'HP:0012769', 'Abnormal arm span', 'XPO:0100900', 'abnormal angioblast', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(314390, 'HP:0012769', 'Abnormal arm span', 'XPO:0100172', 'abnormal stem cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(314391, 'HP:0012769', 'Abnormal arm span', 'XPO:0101547', 'abnormal lampbrush chromosome', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(314392, 'HP:0012769', 'Abnormal arm span', 'XPO:0100031', 'abnormal central nervous system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(314393, 'HP:0012769', 'Abnormal arm span', 'XPO:0100293', 'abnormal duct', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(314394, 'HP:0012769', 'Abnormal arm span', 'XPO:0141266', 'abnormal surface breathing', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(314395, 'HP:0012769', 'Abnormal arm span', 'XPO:0101297', 'abnormal barrier cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(314396, 'HP:0012769', 'Abnormal arm span', 'XPO:0141792', 'abnormal small molecule metabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(314397, 'HP:0012769', 'Abnormal arm span', 'XPO:0141782', 'abnormal methylation', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(314398, 'HP:0012769', 'Abnormal arm span', 'XPO:0100386', 'abnormal limb', 0.5652173913043478, 5.504475013697824, 1.7638664937410224, 'HP:0040064', 'Abnormality of limbs'),
(314399, 'HP:0012769', 'Abnormal arm span', 'XPO:0101157', 'abnormal female organism', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(314400, 'HP:0012769', 'Abnormal arm span', 'XPO:0101497', 'abnormal ciliary axoneme', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(314401, 'HP:0012769', 'Abnormal arm span', 'XPO:0101212', 'abnormal glomeral mesenchyme', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(314402, 'HP:0012769', 'Abnormal arm span', 'XPO:0100429', 'abnormal spermatid', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(314403, 'HP:0012769', 'Abnormal arm span', 'XPO:0100728', 'abnormal cell condensation', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(314404, 'HP:0012769', 'Abnormal arm span', 'XPO:0141264', 'abnormal schooling behavior', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(314405, 'HP:0012769', 'Abnormal arm span', 'XPO:0101362', 'abnormal vegetal cortex', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(314406, 'HP:0012769', 'Abnormal arm span', 'XPO:0101237', 'abnormal mucus secreting cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(314407, 'HP:0012769', 'Abnormal arm span', 'XPO:0141265', 'abnormal escape behavior', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(314408, 'HP:0012769', 'Abnormal arm span', 'XPO:0100135', 'abnormal surface structure', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(314409, 'HP:0012769', 'Abnormal arm span', 'XPO:0107260', 'abnormal anterior-posterior axis', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(314410, 'HP:0012769', 'Abnormal arm span', 'XPO:0131666', 'abnormal adherens junction', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(314411, 'HP:0012769', 'Abnormal arm span', 'XPO:0141267', 'abnormal resting posture', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(314412, 'HP:0012769', 'Abnormal arm span', 'XPO:0100503', 'abnormal blastomere D2', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(314413, 'HP:0012769', 'Abnormal arm span', 'XPO:0100258', 'abnormal organ part', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(314414, 'HP:0012769', 'Abnormal arm span', 'XPO:0100120', 'abnormal genital system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(314415, 'HP:0012769', 'Abnormal arm span', 'XPO:0101264', 'abnormal mitotic spindle', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(314416, 'HP:0012769', 'Abnormal arm span', 'XPO:0100070', 'abnormal anatomical system', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(314417, 'HP:0012769', 'Abnormal arm span', 'XPO:0100531', 'abnormal proliferative region', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(314418, 'HP:0012769', 'Abnormal arm span', 'XPO:0107259', 'abnormal animal-vegetal axis', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(314419, 'HP:0012769', 'Abnormal arm span', 'XPO:0100394', 'abnormal marginal zone', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(314420, 'HP:0012769', 'Abnormal arm span', 'XPO:0107278', 'abnormal medial region', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(314421, 'HP:0012769', 'Abnormal arm span', 'XPO:0100025', 'abnormal oocyte', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(314422, 'HP:0012769', 'Abnormal arm span', 'XPO:0100791', 'abnormal multiciliated cell precursor', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(314423, 'HP:0012769', 'Abnormal arm span', 'XPO:0101136', 'abnormal ooplasm', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(314424, 'HP:0012769', 'Abnormal arm span', 'XPO:0101241', 'abnormal nucleate erythrocyte', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(314425, 'HP:0012769', 'Abnormal arm span', 'XPO:0101240', 'abnormal ciliated non-epidermal cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(314426, 'HP:0012769', 'Abnormal arm span', 'XPO:0100670', 'abnormal forelimb zeugopod', 0.4482758620689655, 5.504475013697824, 1.570835217966058, 'HP:0040064', 'Abnormality of limbs'),
(314427, 'HP:0012769', 'Abnormal arm span', 'XPO:0100162', 'abnormal presumptive rhombomere', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(314428, 'HP:0012769', 'Abnormal arm span', 'XPO:0141271', 'increased surface breathing', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(314429, 'HP:0012769', 'Abnormal arm span', 'XPO:0100533', 'abnormal melanoblast', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(314430, 'HP:0012769', 'Abnormal arm span', 'XPO:0100218', 'abnormal epithelial cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(314431, 'HP:0012769', 'Abnormal arm span', 'XPO:0100852', 'abnormal interdigital region', 0.6190476190476191, 5.504475013697824, 1.8459502028323378, 'HP:0040064', 'Abnormality of limbs'),
(314432, 'HP:0012769', 'Abnormal arm span', 'XPO:0107270', 'abnormal proximal-distal axis', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(314433, 'HP:0012769', 'Abnormal arm span', 'XPO:0100887', 'abnormal right-dorsal blastomere', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(314434, 'HP:0012769', 'Abnormal arm span', 'XPO:0141796', 'abnormal demethylation', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(314435, 'HP:0012769', 'Abnormal arm span', 'XPO:0141772', 'abnormal water homeostasis', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(314436, 'HP:0012769', 'Abnormal arm span', 'XPO:0100976', 'abnormal multiciliated cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(314437, 'HP:0012769', 'Abnormal arm span', 'XPO:0107285', 'abnormal flexural organ', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(314438, 'HP:0012769', 'Abnormal arm span', 'XPO:0100341', 'abnormal hand', 0.4482758620689655, 5.504475013697824, 1.570835217966058, 'HP:0040064', 'Abnormality of limbs'),
(314439, 'HP:0012769', 'Abnormal arm span', 'XPO:0100493', 'abnormal liver and biliary system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(314440, 'HP:0012769', 'Abnormal arm span', 'XPO:0100510', 'abnormal forelimb stylopod', 0.4482758620689655, 5.504475013697824, 1.570835217966058, 'HP:0040064', 'Abnormality of limbs'),
(314441, 'HP:0012769', 'Abnormal arm span', 'XPO:0101326', 'abnormal cementoblast', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(314442, 'HP:0012769', 'Abnormal arm span', 'XPO:0100917', 'abnormal stage III oocyte', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(314443, 'HP:0012769', 'Abnormal arm span', 'XPO:0101472', 'abnormal zygote cortex', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(314444, 'HP:0012769', 'Abnormal arm span', 'XPO:0100842', 'abnormal left-dorsal blastomere', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(314445, 'HP:0012769', 'Abnormal arm span', 'XPO:0107268', 'abnormal left side', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(314446, 'HP:0012769', 'Abnormal arm span', 'XPO:0100653', 'abnormal myoblast', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(314447, 'HP:0012769', 'Abnormal arm span', 'XPO:0100384', 'abnormal amputated tissue', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(314448, 'HP:0012769', 'Abnormal arm span', 'XPO:0100009', 'abnormal multi-tissue structure', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(314449, 'HP:0012769', 'Abnormal arm span', 'XPO:0100192', 'abnormal epithelium', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(314450, 'HP:0012769', 'Abnormal arm span', 'XPO:0107284', 'abnormal migrating myoblast', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(314451, 'HP:0012769', 'Abnormal arm span', 'XPO:0131677', 'abnormal actin filament', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(314452, 'HP:0012769', 'Abnormal arm span', 'XPO:0101040', 'abnormal axial mesoderm', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(314453, 'HP:0012769', 'Abnormal arm span', 'XPO:0141841', 'abnormality of whole organism mass', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(314454, 'HP:0012769', 'Abnormal arm span', 'XPO:0100781', 'abnormal presumptive ectoderm', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(314455, 'HP:0012769', 'Abnormal arm span', 'XPO:0100363', 'abnormal cardiovascular system', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(314456, 'HP:0012769', 'Abnormal arm span', 'XPO:0100754', 'abnormal electrically active cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(314457, 'HP:0012769', 'Abnormal arm span', 'XPO:0107272', 'abnormal axial region', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(314458, 'HP:0012769', 'Abnormal arm span', 'XPO:0107264', 'abnormal anterior side', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(314459, 'HP:0012769', 'Abnormal arm span', 'XPO:0100915', 'abnormal dermal system', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(314460, 'HP:0012769', 'Abnormal arm span', 'XPO:0107253', 'abnormal enteric nervous system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(314461, 'HP:0012769', 'Abnormal arm span', 'XPO:0101468', 'abnormal stage I oocyte', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(314462, 'HP:0012769', 'Abnormal arm span', 'XPO:0100372', 'abnormal hematological system', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(314463, 'HP:0012769', 'Abnormal arm span', 'XPO:0101373', 'abnormal oxygen accumulating cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(314464, 'HP:0012769', 'Abnormal arm span', 'XPO:0116434', 'abnormal biological process', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(314465, 'HP:0012769', 'Abnormal arm span', 'XPO:0100640', 'abnormal notochordal sheath', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(314466, 'HP:0012769', 'Abnormal arm span', 'XPO:0141776', 'abnormal metabolic process', 0.45454545454545453, 1.8210412618256888, 0.9098054891583067, 'HP:0000118', 'Phenotypic abnormality'),
(314467, 'HP:0012769', 'Abnormal arm span', 'XPO:0100081', 'abnormal anatomical entity in vitro', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(314468, 'HP:0012769', 'Abnormal arm span', 'XPO:0100581', 'abnormal immune system', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(314469, 'HP:0012769', 'Abnormal arm span', 'XPO:0100691', 'abnormal keratin accumulating cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(314470, 'HP:0012769', 'Abnormal arm span', 'XPO:0131685', 'abnormal cortical actin cytoskeleton', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(314471, 'HP:0012769', 'Abnormal arm span', 'XPO:0100006', 'abnormal anatomical structure', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(314472, 'HP:0012769', 'Abnormal arm span', 'XPO:0100888', 'abnormal microtubule', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(314473, 'HP:0012769', 'Abnormal arm span', 'XPO:0141904', 'abnormal glucosamine metabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(314474, 'HP:0012769', 'Abnormal arm span', 'XPO:0100026', 'abnormal germ cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(314475, 'HP:0012769', 'Abnormal arm span', 'XPO:0101004', 'abnormal acid secreting cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(314476, 'HP:0012769', 'Abnormal arm span', 'XPO:0101302', 'abnormal subcortical cytoplasm', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(314477, 'HP:0012769', 'Abnormal arm span', 'XPO:0101347', 'abnormal hindlimb region', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(314478, 'HP:0012769', 'Abnormal arm span', 'XPO:0141770', 'abnormal urate homeostasis', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(314479, 'HP:0012769', 'Abnormal arm span', 'XPO:00000000', 'Xenopus phenotype', 0.47058823529411764, 1.4755025719078136, 0.8332791557971614, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(314480, 'HP:0012769', 'Abnormal arm span', 'XPO:0100762', 'abnormal intersomitic region', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(314481, 'HP:0012769', 'Abnormal arm span', 'XPO:0100724', 'abnormal kinetochore', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(314482, 'HP:0012769', 'Abnormal arm span', 'XPO:0107339', 'abnormal yolk platelet', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(314483, 'HP:0012769', 'Abnormal arm span', 'XPO:0101174', 'abnormal articular system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(314484, 'HP:0012769', 'Abnormal arm span', 'XPO:0100004', 'abnormal cell', 0.5, 1.8210412618256888, 0.954212047143005, 'HP:0000118', 'Phenotypic abnormality'),
(314485, 'HP:0012769', 'Abnormal arm span', 'XPO:0100337', 'abnormal zygote', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(314486, 'HP:0012769', 'Abnormal arm span', 'XPO:0100585', 'abnormal elastica externa', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(314487, 'HP:0012769', 'Abnormal arm span', 'XPO:0100282', 'abnormal pelvic girdle primordium', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(314488, 'HP:0012769', 'Abnormal arm span', 'XPO:0100458', 'abnormal autopod', 0.52, 5.504475013697824, 1.6918413067196547, 'HP:0040064', 'Abnormality of limbs'),
(314489, 'HP:0012769', 'Abnormal arm span', 'XPO:0100642', 'abnormal gustatory system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(314490, 'HP:0012769', 'Abnormal arm span', 'XPO:0142056', 'abnormal main body axis', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(314491, 'HP:0012769', 'Abnormal arm span', 'XPO:0100784', 'abnormal left blastomere', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(314492, 'HP:0012769', 'Abnormal arm span', 'XPO:0100104', 'abnormal embryonic structure', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(314493, 'HP:0012769', 'Abnormal arm span', 'XPO:0101570', 'abnormal forelimb region', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(314494, 'HP:0012769', 'Abnormal arm span', 'XPO:0100069', 'abnormal urinary system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(314495, 'HP:0012769', 'Abnormal arm span', 'XPO:0100285', 'abnormal progenitor cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(314496, 'HP:0012769', 'Abnormal arm span', 'XPO:0141715', 'abnormal septum', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(314497, 'HP:0012769', 'Abnormal arm span', 'XPO:0100423', 'abnormal process', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(314498, 'HP:0012769', 'Abnormal arm span', 'XPO:0101409', 'abnormal perivitelline space', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(314499, 'HP:0012769', 'Abnormal arm span', 'XPO:0100856', 'abnormal simple organ', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(314500, 'HP:0012769', 'Abnormal arm span', 'XPO:0141738', 'abnormal carbon dioxide homeostasis', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(314501, 'HP:0012769', 'Abnormal arm span', 'XPO:0141718', 'abnormal posterior notochord', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(314502, 'HP:0012769', 'Abnormal arm span', 'XPO:0100557', 'abnormal prime meridian', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(314503, 'HP:0012769', 'Abnormal arm span', 'XPO:0141745', 'abnormal creatinine homeostasis', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(314504, 'HP:0012769', 'Abnormal arm span', 'XPO:0100114', 'abnormal peripheral nervous system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(314505, 'HP:0012769', 'Abnormal arm span', 'XPO:0100573', 'abnormal extraembryonic structure', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(314506, 'HP:0012769', 'Abnormal arm span', 'XPO:0101176', 'abnormal non-ciliated epithelial cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(314507, 'HP:0012769', 'Abnormal arm span', 'XPO:0127203', 'abnormally localised interdigital region', 0.4482758620689655, 5.504475013697824, 1.570835217966058, 'HP:0040064', 'Abnormality of limbs'),
(314508, 'HP:0012769', 'Abnormal arm span', 'XPO:0100549', 'abnormal mitotic cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(314509, 'HP:0012769', 'Abnormal arm span', 'XPO:0100251', 'abnormal proteinaceous extracellular matrix', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(314510, 'HP:0012769', 'Abnormal arm span', 'XPO:0141662', 'paralysed forelimb', 0.43333333333333335, 5.504475013697824, 1.5444327456822857, 'HP:0040064', 'Abnormality of limbs'),
(314511, 'HP:0012769', 'Abnormal arm span', 'XPO:0101467', 'abnormal alkali secreting cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(314512, 'HP:0012769', 'Abnormal arm span', 'XPO:0141748', 'abnormal gas homeostasis', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(314513, 'HP:0012769', 'Abnormal arm span', 'XPO:0100547', 'abnormal blastomere V2', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(314514, 'HP:0012769', 'Abnormal arm span', 'XPO:0100239', 'abnormal acellular anatomical structure', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(314515, 'HP:0012769', 'Abnormal arm span', 'XPO:0107263', 'abnormal anatomical side', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(314516, 'HP:0012769', 'Abnormal arm span', 'XPO:0101366', 'abnormal morula cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(314517, 'HP:0012769', 'Abnormal arm span', 'XPO:0101569', 'abnormal activin-induced ectoderm', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(314518, 'HP:0012769', 'Abnormal arm span', 'XPO:0101389', 'abnormal wedge region', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(314519, 'HP:0012769', 'Abnormal arm span', 'XPO:0100862', 'abnormal blastomere V1', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(314520, 'HP:0012769', 'Abnormal arm span', 'XPO:0100721', 'abnormal centromere', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(314521, 'HP:0012769', 'Abnormal arm span', 'XPO:0131669', 'abnormal Roux spot', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(314522, 'HP:0012769', 'Abnormal arm span', 'XPO:0100715', 'abnormal ciliated cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(314523, 'HP:0012769', 'Abnormal arm span', 'XPO:0100822', 'abnormal hindlimb zeugopod', 0.4482758620689655, 5.504475013697824, 1.570835217966058, 'HP:0040064', 'Abnormality of limbs'),
(314524, 'HP:0012769', 'Abnormal arm span', 'XPO:0101110', 'abnormal cell-free extract', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(314525, 'HP:0012769', 'Abnormal arm span', 'XPO:0107265', 'abnormal posterior side', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(314526, 'HP:0012769', 'Abnormal arm span', 'XPO:0100545', 'abnormal male organism', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(314527, 'HP:0012769', 'Abnormal arm span', 'XPO:0101503', 'abnormal organ cortex', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(314528, 'HP:0012769', 'Abnormal arm span', 'XPO:0100665', 'abnormal egg jelly', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(314529, 'HP:0012769', 'Abnormal arm span', 'XPO:0101141', 'abnormal Keller explant', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(314530, 'HP:0012769', 'Abnormal arm span', 'XPO:0101519', 'abnormal hypobranchial placode', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(314531, 'HP:0012769', 'Abnormal arm span', 'XPO:0101513', 'abnormal basal body', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(314532, 'HP:0012769', 'Abnormal arm span', 'XPO:0115509', 'abnormally semi-viable whole organism', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(314533, 'HP:0012769', 'Abnormal arm span', 'XPO:0100457', 'abnormal foot', 0.4482758620689655, 5.504475013697824, 1.570835217966058, 'HP:0040064', 'Abnormality of limbs'),
(314534, 'HP:0012769', 'Abnormal arm span', 'XPO:0100587', 'abnormal vestibuloauditory system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(314535, 'HP:0012769', 'Abnormal arm span', 'XPO:0100574', 'abnormal gastrula cell', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(314536, 'HP:0012769', 'Abnormal arm span', 'XPO:0100481', 'abnormal anatomical line', 0.5, 1.706362323152461, 0.9236780616514774, 'UPHENO:0002536', 'abnormal anatomical entity'),
(314537, 'HP:0012769', 'Abnormal arm span', 'XPO:0100416', 'abnormal ligament', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(314538, 'HP:0012769', 'Abnormal arm span', 'XPO:0100515', 'abnormal somatic stem cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(314539, 'HP:0012769', 'Abnormal arm span', 'XPO:0100308', 'abnormal early embryonic cell', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(314540, 'HP:0012769', 'Abnormal arm span', 'XPO:0101405', 'abnormal ring structure', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(314541, 'HP:0012769', 'Abnormal arm span', 'XPO:0142057', 'abnormal desmosome', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(314542, 'HP:0012769', 'Abnormal arm span', 'XPO:0100295', 'abnormal extracellular matrix', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(314543, 'HP:0012769', 'Abnormal arm span', 'XPO:0100674', 'abnormal secondary oogonium', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(314544, 'HP:0012769', 'Abnormal arm span', 'XPO:0100265', 'abnormal sensory epithelial cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(314545, 'HP:0012769', 'Abnormal arm span', 'XPO:0131675', 'abnormal spindle microtubule', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(314546, 'HP:0012769', 'Abnormal arm span', 'XPO:0101132', 'abnormal apoptotic cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(314547, 'HP:0012769', 'Abnormal arm span', 'XPO:0100377', 'abnormal connective tissue', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(314548, 'HP:0012769', 'Abnormal arm span', 'XPO:0100465', 'abnormal skeletal system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(314549, 'HP:0012769', 'Abnormal arm span', 'XPO:0115566', 'abnormal variability of size of forelimb', 0.48148148148148145, 5.504475013697824, 1.6279750564345348, 'HP:0040064', 'Abnormality of limbs'),
(314550, 'HP:0012769', 'Abnormal arm span', 'XPO:0100638', 'abnormal polar body', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(314551, 'HP:0012769', 'Abnormal arm span', 'XPO:0101071', 'abnormal endoplasmic reticulum', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(314552, 'HP:0012769', 'Abnormal arm span', 'XPO:0141743', 'abnormal chemical homeostasis within a tissue', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(314553, 'HP:0012769', 'Abnormal arm span', 'XPO:0101074', 'abnormal germinal vesicle', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(314554, 'HP:0012769', 'Abnormal arm span', 'XPO:0100969', 'abnormal disaggregated/reaggregated ectoderm treated with activin', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(314555, 'HP:0012769', 'Abnormal arm span', 'XPO:0100151', 'abnormal primordium', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(314556, 'HP:0012769', 'Abnormal arm span', 'XPO:0100277', 'abnormal blastocoel', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(314557, 'HP:0012769', 'Abnormal arm span', 'XPO:0101448', 'abnormal myelin accumulating cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(314558, 'HP:0012769', 'Abnormal arm span', 'XPO:0141315', 'abnormal anatomical region', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(314559, 'HP:0012769', 'Abnormal arm span', 'XPO:0107273', 'abnormal basal region', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(314560, 'HP:0012769', 'Abnormal arm span', 'XPO:0100956', 'abnormal centrosome', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(314561, 'HP:0012769', 'Abnormal arm span', 'XPO:0100307', 'abnormal blastomere', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(314562, 'HP:0012769', 'Abnormal arm span', 'XPO:0107276', 'abnormal dorsal region', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(314563, 'HP:0012769', 'Abnormal arm span', 'XPO:0100010', 'abnormal multicellular anatomical structure', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(314564, 'HP:0012769', 'Abnormal arm span', 'XPO:0100989', 'abnormal right blastomere', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(314565, 'HP:0012769', 'Abnormal arm span', 'XPO:0100913', 'abnormal Brachets cleft', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(314566, 'HP:0012769', 'Abnormal arm span', 'XPO:0115508', 'abnormally peramorphic growth of whole organism', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(314567, 'HP:0012769', 'Abnormal arm span', 'XPO:0101411', 'abnormal marginal zone (sensu neural)', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(314568, 'HP:0012769', 'Abnormal arm span', 'XPO:0100422', 'abnormal notochord', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(314569, 'HP:0012769', 'Abnormal arm span', 'XPO:0100912', 'abnormal trabecula', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(314570, 'HP:0012769', 'Abnormal arm span', 'XPO:0115505', 'dead whole organism', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(314571, 'HP:0012769', 'Abnormal arm span', 'XPO:0101109', 'abnormal egg cell-free extract', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(314572, 'HP:0012769', 'Abnormal arm span', 'XPO:0100417', 'abnormal dense regular connective tissue', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(314573, 'HP:0012769', 'Abnormal arm span', 'XPO:0101378', 'abnormal blastomere D1', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(314574, 'HP:0012769', 'Abnormal arm span', 'XPO:0115758', 'abnormally decreased mobility of melanoblast', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(314575, 'HP:0012769', 'Abnormal arm span', 'XPO:0141263', 'abnormal visually guided collision avoidance behavior', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(314576, 'HP:0012769', 'Abnormal arm span', 'XPO:0101113', 'abnormal stage IV oocyte', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(314577, 'HP:0012769', 'Abnormal arm span', 'XPO:0100437', 'abnormal proepicardium', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(314578, 'HP:0012769', 'Abnormal arm span', 'XPO:0100108', 'abnormal cell part', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(314579, 'HP:0012769', 'Abnormal arm span', 'XPO:0100403', 'abnormal forelimb', 0.5, 5.504475013697824, 1.6589868917049684, 'HP:0040064', 'Abnormality of limbs'),
(314580, 'HP:0012769', 'Abnormal arm span', 'XPO:0100060', 'abnormal regenerating tissue', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(314581, 'HP:0012769', 'Abnormal arm span', 'XPO:0141771', 'abnormal urea homeostasis', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(314582, 'HP:0012769', 'Abnormal arm span', 'XPO:0141797', 'abnormal hydrogen metabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(314583, 'HP:0012769', 'Abnormal arm span', 'XPO:0115574', 'abnormal variability of size of hindlimb', 0.48148148148148145, 5.504475013697824, 1.6279750564345348, 'HP:0040064', 'Abnormality of limbs'),
(314584, 'HP:0012769', 'Abnormal arm span', 'XPO:0141781', 'abnormal secondary metabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(314585, 'HP:0012769', 'Abnormal arm span', 'XPO:0100551', 'abnormal oocyte cortex', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(314586, 'HP:0012769', 'Abnormal arm span', 'XPO:0100898', 'abnormal hindlimb stylopod', 0.4482758620689655, 5.504475013697824, 1.570835217966058, 'HP:0040064', 'Abnormality of limbs'),
(314587, 'HP:0012769', 'Abnormal arm span', 'XPO:0131691', 'abnormal molecular function', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(314588, 'HP:0012769', 'Abnormal arm span', 'XPO:0101480', 'abnormal stage V oocyte', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(314589, 'HP:0012769', 'Abnormal arm span', 'XPO:0101200', 'abnormal joint region', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(314590, 'HP:0012769', 'Abnormal arm span', 'XPO:0115512', 'abnormally semi-erect whole organism', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(314591, 'HP:0012769', 'Abnormal arm span', 'XPO:0100028', 'abnormal anatomical cluster', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(314592, 'HP:0012769', 'Abnormal arm span', 'XPO:0101461', 'abnormal sperm entry point', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(314593, 'HP:0012769', 'Abnormal arm span', 'XPO:0100902', 'abnormal spermatocyte', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(314594, 'HP:0012769', 'Abnormal arm span', 'XPO:0131667', 'abnormal actin cytoskeleton', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(314595, 'HP:0012769', 'Abnormal arm span', 'XPO:0100991', 'abnormal iliac process primordium', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(314596, 'HP:0012769', 'Abnormal arm span', 'XPO:0101311', 'abnormal bottle cell', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(314597, 'HP:0012769', 'Abnormal arm span', 'XPO:0107312', 'abnormal filopodium', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(314598, 'HP:0012769', 'Abnormal arm span', 'XPO:0101575', 'abnormal vitelline membrane', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(314599, 'HP:0012769', 'Abnormal arm span', 'XPO:0131723', 'abnormal pathway-restricted SMAD protein phosphorylation', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(314600, 'HP:0012769', 'Abnormal arm span', 'XPO:0100742', 'abnormal musculoskeletal system', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(314601, 'HP:0012769', 'Abnormal arm span', 'XPO:0100402', 'abnormal zeugopod', 0.52, 5.504475013697824, 1.6918413067196547, 'HP:0040064', 'Abnormality of limbs'),
(314602, 'HP:0012769', 'Abnormal arm span', 'XPO:0100186', 'abnormal uveal tract', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(314603, 'HP:0012769', 'Abnormal arm span', 'XPO:0100823', 'abnormal blood', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(314604, 'HP:0012769', 'Abnormal arm span', 'XPO:0100339', 'abnormal circumblastoporal collar', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(314605, 'HP:0012769', 'Abnormal arm span', 'XPO:0100415', 'abnormal secretory epithelial cell', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(314606, 'HP:0012769', 'Abnormal arm span', 'XPO:0100152', 'abnormal alimentary system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(314607, 'HP:0012769', 'Abnormal arm span', 'XPO:0100546', 'abnormal whole organism', 0.47368421052631576, 1.706362323152461, 0.8990422069704646, 'UPHENO:0002536', 'abnormal anatomical entity'),
(314608, 'HP:0012769', 'Abnormal arm span', 'XPO:0100802', 'abnormal exocrine cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(314609, 'HP:0012769', 'Abnormal arm span', 'XPO:0107266', 'abnormal dorsal side', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(314610, 'HP:0012769', 'Abnormal arm span', 'XPO:0107262', 'abnormal left-right axis', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(314611, 'HP:0012769', 'Abnormal arm span', 'XPO:0101498', 'abnormal stage II oocyte', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(314612, 'HP:0012769', 'Abnormal arm span', 'XPO:0100014', 'abnormal tissue', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(314613, 'HP:0012769', 'Abnormal arm span', 'XPO:0100643', 'abnormal thoracic region', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(314614, 'HP:0012769', 'Abnormal arm span', 'XPO:0100032', 'abnormal nervous system', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(314615, 'HP:0012769', 'Abnormal arm span', 'XPO:0100511', 'abnormal stylopod', 0.52, 5.504475013697824, 1.6918413067196547, 'HP:0040064', 'Abnormality of limbs'),
(314616, 'HP:0012769', 'Abnormal arm span', 'XPO:0100477', 'abnormal pericyte', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(314617, 'HP:0012769', 'Abnormal arm span', 'XPO:0141778', 'abnormal biosynthetic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(314618, 'HP:0012769', 'Abnormal arm span', 'XPO:0101435', 'abnormal paracrine cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(314619, 'HP:0012769', 'Abnormal arm span', 'XPO:0107269', 'abnormal right side', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(314620, 'HP:0012769', 'Abnormal arm span', 'XPO:0141276', 'decreased surface breathing', 0.42105263157894735, 1.4755025719078136, 0.7882031722869998, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(314621, 'HP:0012769', 'Abnormal arm span', 'XPO:0100704', 'abnormal Merkel cell', 0.4782608695652174, 1.8210412618256888, 0.9332377925239069, 'HP:0000118', 'Phenotypic abnormality'),
(314622, 'HP:0012769', 'Abnormal arm span', 'XPO:0100274', 'abnormal sensory system', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(314623, 'HP:0012769', 'Abnormal arm span', 'XPO:0100427', 'abnormal olfactory system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(314624, 'HP:0012769', 'Abnormal arm span', 'XPO:0142052', 'abnormal nasal region', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(314625, 'HP:0012769', 'Abnormal arm span', 'XPO:0101451', 'abnormal dorsal lymph space', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(314626, 'HP:0012769', 'Abnormal arm span', 'XPO:0100023', 'abnormal mesenchyme', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(314627, 'HP:0012769', 'Abnormal arm span', 'XPO:0107271', 'abnormal apical region', 0.42857142857142855, 1.706362323152461, 0.8551597151958877, 'UPHENO:0002536', 'abnormal anatomical entity'),
(314628, 'HP:0012769', 'Abnormal arm span', 'XPO:0141794', 'abnormal prosthetic group metabolic process', 0.4166666666666667, 1.8210412618256888, 0.871072438105678, 'HP:0000118', 'Phenotypic abnormality'),
(314629, 'HP:0012769', 'Abnormal arm span', 'XPO:0101220', 'abnormal centriole', 0.44, 1.8210412618256888, 0.8951302448265857, 'HP:0000118', 'Phenotypic abnormality'),
(314630, 'HP:0012769', 'Abnormal arm span', 'XPO:0100202', 'abnormal embryo', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(314631, 'HP:0012769', 'Abnormal arm span', 'XPO:0100688', 'abnormal adipose tissue', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(314632, 'HP:0012769', 'Abnormal arm span', 'XPO:0142051', 'abnormal cerebrospinal fluid', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(314633, 'HP:0012769', 'Abnormal arm span', 'XPO:0107261', 'abnormal dorsal-ventral axis', 0.45, 1.706362323152461, 0.8762779498644294, 'UPHENO:0002536', 'abnormal anatomical entity'),
(314634, 'HP:0012769', 'Abnormal arm span', 'XPO:0115391', 'abnormally undifferentiated alimentary system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(314635, 'HP:0012769', 'Abnormal arm span', 'XPO:0107288', 'abnormal larval alimentary system', 0.4074074074074074, 1.8210412618256888, 0.861339479684008, 'HP:0000118', 'Phenotypic abnormality'),
(314636, 'HP:0012769', 'Abnormal arm span', 'XPO:0100273', 'abnormal visual system', 0.4230769230769231, 1.8210412618256888, 0.8777474203034321, 'HP:0000118', 'Phenotypic abnormality'),
(314637, 'HP:0012769', 'Abnormal arm span', 'XPO:0107267', 'abnormal ventral side', 0.4090909090909091, 1.706362323152461, 0.8354982429765582, 'UPHENO:0002536', 'abnormal anatomical entity'),
(314638, 'HP:0012769', 'Abnormal arm span', 'XPO:0100317', 'abnormal respiratory system', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(314639, 'HP:0012769', 'Abnormal arm span', 'XPO:0100894', 'abnormal nucleus', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
(314640, 'HP:0012769', 'Abnormal arm span', 'XPO:0131725', 'abnormal phosphorylation of RNA polymerase II C-terminal domain', 0.4444444444444444, 1.4755025719078136, 0.8098017787384251, 'UPHENO:0001005', 'abnormal phenotype by ontology source'),
(314641, 'HP:0012769', 'Abnormal arm span', 'XPO:0100899', 'abnormal secondary spermatogonium', 0.4583333333333333, 1.8210412618256888, 0.9135884804823818, 'HP:0000118', 'Phenotypic abnormality'),
