{"context":{"query":">>hgnc>>hpo","source_dataset":"hgnc","target_dataset":"hpo"},"stats":{"queried":1,"total":17,"mapped":1},"pagination":{"has_next":false},"schema":"id|name|definition","mappings":[{"input":"HGNC:11283","source":"HGNC:11283|SRC proto-oncogene, non-receptor tyrosine kinase","targets":["HP:0000006|Autosomal dominant inheritance|","HP:0000490|Deeply set eye|","HP:0000601|Hypotelorism|","HP:0000939|Osteoporosis|","HP:0001442|Typified by somatic mosaicism|","HP:0001873|Thrombocytopenia|","HP:0001892|Abnormal bleeding|","HP:0002003|Large forehead|","HP:0002891|Uterine leiomyosarcoma|","HP:0003003|Colon cancer|","HP:0004406|Spontaneous, recurrent epistaxis|","HP:0005584|Renal cell carcinoma|","HP:0006716|Hereditary nonpolyposis colorectal carcinoma|","HP:0006740|Transitional cell carcinoma of the bladder|","HP:0006753|Neoplasm of the stomach|","HP:0011974|Myelofibrosis|","HP:0031020|Bone marrow hypercellularity|"]}]}