{"context":{"query":">>hgnc>>gencc","source_dataset":"hgnc","target_dataset":"gencc"},"stats":{"queried":1,"total":14,"mapped":1},"pagination":{"has_next":false},"schema":"id|gene_symbol|disease_title|classification_title|moi_title|submitter_title","mappings":[{"input":"HGNC:9967","source":"HGNC:9967|ret proto-oncogene","targets":["GENCC_000106-HGNC_9967-OMIM_142623-HP_0000006-GENCC_100002|RET|Hirschsprung disease, susceptibility to, 1|Strong|Autosomal dominant|Labcorp Genetics (formerly Invitae)","GENCC_000106-HGNC_9967-OMIM_162300-HP_0000006-GENCC_100002|RET|multiple endocrine neoplasia type 2B|Strong|Autosomal dominant|Labcorp Genetics (formerly Invitae)","GENCC_000110-HGNC_9967-ORPHANET_1848-HP_0000007-GENCC_100009|RET|bilateral renal agenesis|Supportive|Autosomal recessive|Orphanet","GENCC_000110-HGNC_9967-ORPHANET_247698-HP_0000006-GENCC_100009|RET|multiple endocrine neoplasia type 2A|Supportive|Autosomal dominant|Orphanet","GENCC_000110-HGNC_9967-ORPHANET_247709-HP_0000006-GENCC_100009|RET|multiple endocrine neoplasia type 2B|Supportive|Autosomal dominant|Orphanet","GENCC_000110-HGNC_9967-ORPHANET_388-HP_0000006-GENCC_100009|RET|Hirschsprung disease|Supportive|Autosomal dominant|Orphanet","GENCC_000110-HGNC_9967-ORPHANET_93100-HP_0000006-GENCC_100009|RET|renal agenesis, unilateral|Supportive|Autosomal dominant|Orphanet","GENCC_000110-HGNC_9967-ORPHANET_99361-HP_0000006-GENCC_100009|RET|familial medullary thyroid carcinoma|Supportive|Autosomal dominant|Orphanet","GENCC_000110-HGNC_9967-ORPHANET_99803-HP_0000006-GENCC_100009|RET|Haddad syndrome|Supportive|Autosomal dominant|Orphanet","GENCC_000112-HGNC_9967-MONDO_0008233-HP_0000006-GENCC_100001|RET|pheochromocytoma|Definitive|Autosomal dominant|G2P","GENCC_000112-HGNC_9967-MONDO_0018470-HP_0000007-GENCC_100004|RET|renal agenesis|Limited|Autosomal recessive|G2P","GENCC_000112-HGNC_9967-OMIM_155240-HP_0000006-GENCC_100001|RET|familial medullary thyroid carcinoma|Definitive|Autosomal dominant|G2P","GENCC_000112-HGNC_9967-OMIM_162300-HP_0000006-GENCC_100001|RET|multiple endocrine neoplasia type 2B|Definitive|Autosomal dominant|G2P","GENCC_000112-HGNC_9967-OMIM_171400-HP_0000006-GENCC_100001|RET|multiple endocrine neoplasia type 2A|Definitive|Autosomal dominant|G2P"]}]}