{"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:644","source":"HGNC:644|androgen receptor","targets":["GENCC_000101-HGNC_644-OMIM_300068-HP_0001417-GENCC_100001|AR|androgen insensitivity syndrome|Definitive|X-linked|Ambry Genetics","GENCC_000101-HGNC_644-OMIM_313200-HP_0001417-GENCC_100002|AR|Kennedy disease|Strong|X-linked|Ambry Genetics","GENCC_000104-HGNC_644-OMIM_312300-HP_0001417-GENCC_100002|AR|partial androgen insensitivity syndrome|Strong|X-linked|Genomics England PanelApp","GENCC_000106-HGNC_644-OMIM_300068-HP_0001417-GENCC_100002|AR|androgen insensitivity syndrome|Strong|X-linked|Labcorp Genetics (formerly Invitae)","GENCC_000106-HGNC_644-OMIM_313200-HP_0001417-GENCC_100002|AR|Kennedy disease|Strong|X-linked|Labcorp Genetics (formerly Invitae)","GENCC_000107-HGNC_644-OMIM_300068-HP_0001417-GENCC_100002|AR|androgen insensitivity syndrome|Strong|X-linked|Laboratory for Molecular Medicine","GENCC_000110-HGNC_644-ORPHANET_481-HP_0001417-GENCC_100009|AR|Kennedy disease|Supportive|X-linked|Orphanet","GENCC_000110-HGNC_644-ORPHANET_90797-HP_0001417-GENCC_100009|AR|partial androgen insensitivity syndrome|Supportive|X-linked|Orphanet","GENCC_000110-HGNC_644-ORPHANET_99429-HP_0001417-GENCC_100009|AR|complete androgen insensitivity syndrome|Supportive|X-linked|Orphanet","GENCC_000112-HGNC_644-OMIM_300068-HP_0001417-GENCC_100001|AR|androgen insensitivity syndrome|Definitive|X-linked|G2P","GENCC_000112-HGNC_644-OMIM_313200-HP_0001417-GENCC_100001|AR|Kennedy disease|Definitive|X-linked|G2P"]}]}