{"context":{"query":">>hgnc>>gencc","source_dataset":"hgnc","target_dataset":"gencc"},"stats":{"queried":1,"total":4,"mapped":1},"pagination":{"has_next":false},"schema":"id|gene_symbol|disease_title|classification_title|moi_title|submitter_title","mappings":[{"input":"HGNC:391","source":"HGNC:391|AKT serine/threonine kinase 1","targets":["GENCC_000106-HGNC_391-OMIM_176920-HP_0000006-GENCC_100002|AKT1|Proteus syndrome|Strong|Autosomal dominant|Labcorp Genetics (formerly Invitae)","GENCC_000106-HGNC_391-OMIM_615109-HP_0000005-GENCC_100004|AKT1|Cowden syndrome 6|Limited|Unknown|Labcorp Genetics (formerly Invitae)","GENCC_000110-HGNC_391-ORPHANET_201-HP_0000006-GENCC_100009|AKT1|Cowden disease|Supportive|Autosomal dominant|Orphanet","GENCC_000112-HGNC_391-OMIM_176920-HP_0000006-GENCC_100001|AKT1|Proteus syndrome|Definitive|Autosomal dominant|G2P"]}]}