{"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:2928","source":"HGNC:2928|dystrophin","targets":["GENCC_000101-HGNC_2928-OMIM_300376-HP_0001417-GENCC_100001|DMD|Becker muscular dystrophy|Definitive|X-linked|Ambry Genetics","GENCC_000101-HGNC_2928-OMIM_302045-HP_0001417-GENCC_100001|DMD|dilated cardiomyopathy 3B|Definitive|X-linked|Ambry Genetics","GENCC_000101-HGNC_2928-OMIM_310200-HP_0001417-GENCC_100001|DMD|Duchenne muscular dystrophy|Definitive|X-linked|Ambry Genetics","GENCC_000106-HGNC_2928-OMIM_310200-HP_0001417-GENCC_100002|DMD|Duchenne muscular dystrophy|Strong|X-linked|Labcorp Genetics (formerly Invitae)","GENCC_000108-HGNC_2928-MONDO_0016899-HP_0001417-GENCC_100001|DMD|Duchenne and Becker muscular dystrophy|Definitive|X-linked|Myriad Women’s Health","GENCC_000110-HGNC_2928-ORPHANET_154-HP_0000006-GENCC_100009|DMD|familial isolated dilated cardiomyopathy|Supportive|Autosomal dominant|Orphanet","GENCC_000110-HGNC_2928-ORPHANET_206546-HP_0001417-GENCC_100009|DMD|symptomatic form of muscular dystrophy of Duchenne and Becker in female carriers|Supportive|X-linked|Orphanet","GENCC_000110-HGNC_2928-ORPHANET_777-HP_0001417-GENCC_100009|DMD|non-syndromic X-linked intellectual disability|Supportive|X-linked|Orphanet","GENCC_000110-HGNC_2928-ORPHANET_98895-HP_0001417-GENCC_100009|DMD|Becker muscular dystrophy|Supportive|X-linked|Orphanet","GENCC_000110-HGNC_2928-ORPHANET_98896-HP_0001417-GENCC_100009|DMD|Duchenne muscular dystrophy|Supportive|X-linked|Orphanet","GENCC_000112-HGNC_2928-OMIM_310200-HP_0001417-GENCC_100001|DMD|Duchenne muscular dystrophy|Definitive|X-linked|G2P"]}]}