{"context":{"query":">>hgnc>>gencc","source_dataset":"hgnc","target_dataset":"gencc"},"stats":{"queried":1,"total":11,"mapped":1},"pagination":{"has_next":false},"schema":"id|gene_symbol|disease_title|classification_title|moi_title|submitter_title","mappings":[{"input":"HGNC:12687","source":"HGNC:12687|von Hippel-Lindau tumor suppressor","targets":["GENCC_000101-HGNC_12687-MONDO_0016598-HP_0000007-GENCC_100002|VHL|autosomal recessive secondary polycythemia not associated with VHL gene|Strong|Autosomal recessive|Ambry Genetics","GENCC_000104-HGNC_12687-MONDO_0005086-HP_0000006-GENCC_100002|VHL|renal cell carcinoma|Strong|Autosomal dominant|Genomics England PanelApp","GENCC_000104-HGNC_12687-OMIM_193300-HP_0000006-GENCC_100002|VHL|von Hippel-Lindau disease|Strong|Autosomal dominant|Genomics England PanelApp","GENCC_000104-HGNC_12687-OMIM_263400-HP_0000007-GENCC_100002|VHL|Chuvash polycythemia|Strong|Autosomal recessive|Genomics England PanelApp","GENCC_000106-HGNC_12687-OMIM_193300-HP_0000006-GENCC_100002|VHL|von Hippel-Lindau disease|Strong|Autosomal dominant|Labcorp Genetics (formerly Invitae)","GENCC_000106-HGNC_12687-OMIM_263400-HP_0000007-GENCC_100002|VHL|Chuvash polycythemia|Strong|Autosomal recessive|Labcorp Genetics (formerly Invitae)","GENCC_000110-HGNC_12687-ORPHANET_238557-HP_0000007-GENCC_100009|VHL|Chuvash polycythemia|Supportive|Autosomal recessive|Orphanet","GENCC_000110-HGNC_12687-ORPHANET_29072-HP_0000006-GENCC_100009|VHL|hereditary pheochromocytoma-paraganglioma|Supportive|Autosomal dominant|Orphanet","GENCC_000110-HGNC_12687-ORPHANET_892-HP_0000006-GENCC_100009|VHL|von Hippel-Lindau disease|Supportive|Autosomal dominant|Orphanet","GENCC_000112-HGNC_12687-MONDO_0008233-HP_0000006-GENCC_100001|VHL|pheochromocytoma|Definitive|Autosomal dominant|G2P","GENCC_000112-HGNC_12687-OMIM_193300-HP_0000006-GENCC_100001|VHL|von Hippel-Lindau disease|Definitive|Autosomal dominant|G2P"]}]}