{"context":{"query":">>hgnc>>gencc","source_dataset":"hgnc","target_dataset":"gencc"},"stats":{"queried":1,"total":23,"mapped":1},"pagination":{"has_next":false},"schema":"id|gene_symbol|disease_title|classification_title|moi_title|submitter_title","mappings":[{"input":"HGNC:10593","source":"HGNC:10593|sodium voltage-gated channel alpha subunit 5","targets":["GENCC_000101-HGNC_10593-OMIM_113900-HP_0032113-GENCC_100003|SCN5A|progressive familial heart block, type 1A|Moderate|Semidominant|Ambry Genetics","GENCC_000101-HGNC_10593-OMIM_601144-HP_0000006-GENCC_100001|SCN5A|Brugada syndrome 1|Definitive|Autosomal dominant|Ambry Genetics","GENCC_000101-HGNC_10593-OMIM_601154-HP_0000006-GENCC_100001|SCN5A|dilated cardiomyopathy 1E|Definitive|Autosomal dominant|Ambry Genetics","GENCC_000101-HGNC_10593-OMIM_603830-HP_0000006-GENCC_100001|SCN5A|long QT syndrome 3|Definitive|Autosomal dominant|Ambry Genetics","GENCC_000102-HGNC_10593-MONDO_0015263-HP_0000006-GENCC_100001|SCN5A|Brugada syndrome|Definitive|Autosomal dominant|ClinGen","GENCC_000104-HGNC_10593-OMIM_113900-HP_0000006-GENCC_100002|SCN5A|progressive familial heart block, type 1A|Strong|Autosomal dominant|Genomics England PanelApp","GENCC_000104-HGNC_10593-OMIM_601144-HP_0000006-GENCC_100002|SCN5A|Brugada syndrome 1|Strong|Autosomal dominant|Genomics England PanelApp","GENCC_000106-HGNC_10593-OMIM_601144-HP_0000006-GENCC_100002|SCN5A|Brugada syndrome 1|Strong|Autosomal dominant|Labcorp Genetics (formerly Invitae)","GENCC_000106-HGNC_10593-OMIM_601154-HP_0000006-GENCC_100002|SCN5A|dilated cardiomyopathy 1E|Strong|Autosomal dominant|Labcorp Genetics (formerly Invitae)","GENCC_000106-HGNC_10593-OMIM_603830-HP_0000006-GENCC_100002|SCN5A|long QT syndrome 3|Strong|Autosomal dominant|Labcorp Genetics (formerly Invitae)","GENCC_000106-HGNC_10593-OMIM_608567-HP_0000006-GENCC_100004|SCN5A|sick sinus syndrome 1|Limited|Autosomal dominant|Labcorp Genetics (formerly Invitae)","GENCC_000106-HGNC_10593-OMIM_608567-HP_0000007-GENCC_100002|SCN5A|sick sinus syndrome 1|Strong|Autosomal recessive|Labcorp Genetics (formerly Invitae)","GENCC_000107-HGNC_10593-OMIM_601144-HP_0000006-GENCC_100001|SCN5A|Brugada syndrome 1|Definitive|Autosomal dominant|Laboratory for Molecular Medicine","GENCC_000110-HGNC_10593-ORPHANET_130-HP_0000006-GENCC_100009|SCN5A|Brugada syndrome|Supportive|Autosomal dominant|Orphanet","GENCC_000110-HGNC_10593-ORPHANET_1344-HP_0000006-GENCC_100009|SCN5A|atrial standstill|Supportive|Autosomal dominant|Orphanet","GENCC_000110-HGNC_10593-ORPHANET_154-HP_0000006-GENCC_100009|SCN5A|familial isolated dilated cardiomyopathy|Supportive|Autosomal dominant|Orphanet","GENCC_000110-HGNC_10593-ORPHANET_166282-HP_0000006-GENCC_100009|SCN5A|familial sick sinus syndrome|Supportive|Autosomal dominant|Orphanet","GENCC_000110-HGNC_10593-ORPHANET_228140-HP_0000006-GENCC_100009|SCN5A|paroxysmal familial ventricular fibrillation|Supportive|Autosomal dominant|Orphanet","GENCC_000110-HGNC_10593-ORPHANET_334-HP_0000006-GENCC_100009|SCN5A|familial atrial fibrillation|Supportive|Autosomal dominant|Orphanet","GENCC_000110-HGNC_10593-ORPHANET_871-HP_0000006-GENCC_100009|SCN5A|progressive familial heart block|Supportive|Autosomal dominant|Orphanet","GENCC_000112-HGNC_10593-MONDO_0011001-HP_0000006-GENCC_100001|SCN5A|Brugada syndrome 1|Definitive|Autosomal dominant|G2P","GENCC_000112-HGNC_10593-MONDO_0011003-HP_0000006-GENCC_100001|SCN5A|dilated cardiomyopathy 1E|Definitive|Autosomal dominant|G2P","GENCC_000112-HGNC_10593-MONDO_0011377-HP_0000006-GENCC_100001|SCN5A|long QT syndrome 3|Definitive|Autosomal dominant|G2P"]}]}