{"context":{"query":">>hgnc>>gencc","source_dataset":"hgnc","target_dataset":"gencc"},"stats":{"queried":1,"total":13,"mapped":1},"pagination":{"has_next":false},"schema":"id|gene_symbol|disease_title|classification_title|moi_title|submitter_title","mappings":[{"input":"HGNC:6770","source":"HGNC:6770|SMAD family member 4","targets":["GENCC_000104-HGNC_6770-OMIM_174900-HP_0000006-GENCC_100002|SMAD4|generalized juvenile polyposis/juvenile polyposis coli|Strong|Autosomal dominant|Genomics England PanelApp","GENCC_000104-HGNC_6770-OMIM_175050-HP_0000006-GENCC_100002|SMAD4|juvenile polyposis/hereditary hemorrhagic telangiectasia syndrome|Strong|Autosomal dominant|Genomics England PanelApp","GENCC_000106-HGNC_6770-OMIM_139210-HP_0000006-GENCC_100002|SMAD4|Myhre syndrome|Strong|Autosomal dominant|Labcorp Genetics (formerly Invitae)","GENCC_000106-HGNC_6770-OMIM_174900-HP_0000006-GENCC_100002|SMAD4|juvenile polyposis syndrome|Strong|Autosomal dominant|Labcorp Genetics (formerly Invitae)","GENCC_000106-HGNC_6770-OMIM_175050-HP_0000006-GENCC_100002|SMAD4|juvenile polyposis/hereditary hemorrhagic telangiectasia syndrome|Strong|Autosomal dominant|Labcorp Genetics (formerly Invitae)","GENCC_000110-HGNC_6770-ORPHANET_2588-HP_0000006-GENCC_100009|SMAD4|Myhre syndrome|Supportive|Autosomal dominant|Orphanet","GENCC_000110-HGNC_6770-ORPHANET_329971-HP_0000006-GENCC_100009|SMAD4|generalized juvenile polyposis/juvenile polyposis coli|Supportive|Autosomal dominant|Orphanet","GENCC_000110-HGNC_6770-ORPHANET_774-HP_0000006-GENCC_100009|SMAD4|hereditary hemorrhagic telangiectasia|Supportive|Autosomal dominant|Orphanet","GENCC_000110-HGNC_6770-ORPHANET_91387-HP_0000006-GENCC_100009|SMAD4|familial thoracic aortic aneurysm and aortic dissection|Supportive|Autosomal dominant|Orphanet","GENCC_000111-HGNC_6770-OMIM_139210-HP_0000006-GENCC_100002|SMAD4|Myhre syndrome|Strong|Autosomal dominant|PanelApp Australia","GENCC_000111-HGNC_6770-OMIM_175050-HP_0000006-GENCC_100002|SMAD4|juvenile polyposis/hereditary hemorrhagic telangiectasia syndrome|Strong|Autosomal dominant|PanelApp Australia","GENCC_000112-HGNC_6770-OMIM_139210-HP_0000006-GENCC_100001|SMAD4|Myhre syndrome|Definitive|Autosomal dominant|G2P","GENCC_000112-HGNC_6770-OMIM_175050-HP_0000006-GENCC_100001|SMAD4|juvenile polyposis/hereditary hemorrhagic telangiectasia syndrome|Definitive|Autosomal dominant|G2P"]}]}