{"context":{"query":">>hgnc>>gencc","source_dataset":"hgnc","target_dataset":"gencc"},"stats":{"queried":1,"total":6,"mapped":1},"pagination":{"has_next":false},"schema":"id|gene_symbol|disease_title|classification_title|moi_title|submitter_title","mappings":[{"input":"HGNC:4851","source":"HGNC:4851|huntingtin","targets":["GENCC_000101-HGNC_4851-OMIM_143100-HP_0000006-GENCC_100001|HTT|Huntington disease|Definitive|Autosomal dominant|Ambry Genetics","GENCC_000101-HGNC_4851-OMIM_617435-HP_0000007-GENCC_100004|HTT|Lopes-Maciel-Rodan syndrome|Limited|Autosomal recessive|Ambry Genetics","GENCC_000106-HGNC_4851-OMIM_143100-HP_0000006-GENCC_100002|HTT|Huntington disease|Strong|Autosomal dominant|Labcorp Genetics (formerly Invitae)","GENCC_000106-HGNC_4851-OMIM_617435-HP_0000007-GENCC_100002|HTT|Lopes-Maciel-Rodan syndrome|Strong|Autosomal recessive|Labcorp Genetics (formerly Invitae)","GENCC_000110-HGNC_4851-ORPHANET_248111-HP_0000006-GENCC_100009|HTT|juvenile Huntington disease|Supportive|Autosomal dominant|Orphanet","GENCC_000110-HGNC_4851-ORPHANET_399-HP_0000006-GENCC_100009|HTT|Huntington disease|Supportive|Autosomal dominant|Orphanet"]}]}