{"context":{"query":">>hgnc>>hpo","source_dataset":"hgnc","target_dataset":"hpo"},"stats":{"queried":1,"total":100,"mapped":1},"pagination":{"has_next":true,"next_token":"-1[]HGNC:6342,10,HGNC:6342,150,3]["},"schema":"id|name|definition","mappings":[{"input":"HGNC:6342","source":"HGNC:6342|KIT proto-oncogene, receptor tyrosine kinase","targets":["HP:0000006|Autosomal dominant inheritance|","HP:0000027|Azoospermia|","HP:0000252|Microcephaly|","HP:0000343|Long philtrum|","HP:0000365|Hearing impairment|","HP:0000431|Wide nasal bridge|","HP:0000598|Abnormality of the ear|","HP:0000664|Synophrys|","HP:0000939|Osteoporosis|","HP:0000953|Hyperpigmentation of the skin|","HP:0000969|Edema|","HP:0000980|Pallor|","HP:0000988|Skin rash|","HP:0000989|Pruritus|","HP:0001019|Erythroderma|","HP:0001025|Urticaria|","HP:0001034|Hypermelanotic macule|","HP:0001053|Hypopigmented skin patches|","HP:0001067|Neurofibroma|","HP:0001072|Thickened skin|","HP:0001100|Heterochromia iridis|","HP:0001176|Large hands|","HP:0001249|Intellectual disability|","HP:0001251|Ataxia|","HP:0001252|Hypotonia|","HP:0001279|Syncope|","HP:0001392|Abnormality of the liver|","HP:0001442|Typified by somatic mosaicism|","HP:0001649|Tachycardia|","HP:0001744|Splenomegaly|","HP:0001824|Weight loss|","HP:0001873|Thrombocytopenia|","HP:0001880|Increased total eosinophil count|","HP:0001895|Normochromic anemia|","HP:0001897|Normocytic anemia|","HP:0001903|Anemia|","HP:0001945|Fever|","HP:0001974|Increased total leukocyte count|","HP:0002013|Vomiting|","HP:0002014|Diarrhea|","HP:0002015|Dysphagia|","HP:0002017|Nausea and vomiting|","HP:0002018|Nausea|","HP:0002019|Constipation|","HP:0002027|Abdominal pain|","HP:0002086|Abnormality of the respiratory system|","HP:0002094|Dyspnea|","HP:0002211|White forelock|","HP:0002226|White eyebrow|","HP:0002227|White eyelashes|","HP:0002239|Gastrointestinal hemorrhage|","HP:0002240|Hepatomegaly|","HP:0002251|Aganglionic megacolon|","HP:0002315|Headache|","HP:0002615|Hypotension|","HP:0002653|Bone pain|","HP:0002659|Increased susceptibility to fractures|","HP:0002664|Neoplasm|","HP:0002665|Lymphoma|","HP:0002683|Abnormal calvaria morphology|","HP:0002716|Lymphadenopathy|","HP:0002829|Arthralgia|","HP:0002863|Myelodysplasia|","HP:0002898|Embryonal neoplasm|","HP:0003326|Myalgia|","HP:0003745|Sporadic|","HP:0004377|Hematological neoplasm|","HP:0004398|Peptic ulcer|","HP:0004808|Acute myeloid leukemia|","HP:0005214|Intestinal obstruction|","HP:0005547|Myeloproliferative disorder|","HP:0005550|Chronic lymphatic leukemia|","HP:0005587|Profuse pigmented skin lesions|","HP:0005599|Hypopigmentation of hair|","HP:0006254|Elevated circulating alpha-fetoprotein concentration|","HP:0006543|Cardiorespiratory arrest|","HP:0006753|Neoplasm of the stomach|","HP:0006775|Multiple myeloma|","HP:0007378|Neoplasm of the gastrointestinal tract|","HP:0007400|Irregular hyperpigmentation|","HP:0007443|Partial albinism|","HP:0007542|Absent pigmentation of the ventral chest|","HP:0007544|Piebald skin depigmentation|","HP:0007583|Telangiectasia macularis eruptiva perstans|","HP:0008066|Abnormal blistering of the skin|","HP:0008069|Neoplasm of the skin|","HP:0009792|Teratoma|","HP:0010783|Erythema|","HP:0011034|Amyloid deposition|","HP:0011897|Increased total neutrophil count|","HP:0011971|Dermatographic urticaria|","HP:0012138|Granulocytic hyperplasia|","HP:0012324|Myeloid leukemia|","HP:0012325|Chronic myelomonocytic leukemia|","HP:0012378|Fatigue|","HP:0012733|Macule|","HP:0025081|Darier's sign|","HP:0025473|Hyperpigmented papule|","HP:0025533|Peau d'orange|","HP:0030350|Erythematous papule|"]}]}