{"context":{"query":">>hgnc>>gencc","source_dataset":"hgnc","target_dataset":"gencc"},"stats":{"queried":1,"total":8,"mapped":1},"pagination":{"has_next":false},"schema":"id|gene_symbol|disease_title|classification_title|moi_title|submitter_title","mappings":[{"input":"HGNC:7881","source":"HGNC:7881|notch receptor 1","targets":["GENCC_000101-HGNC_7881-MONDO_0019046-HP_0000006-GENCC_100003|NOTCH1|leukodystrophy|Moderate|Autosomal dominant|Ambry Genetics","GENCC_000104-HGNC_7881-MONDO_0003900-HP_0000006-GENCC_100003|NOTCH1|connective tissue disorder|Moderate|Autosomal dominant|Genomics England PanelApp","GENCC_000105-HGNC_7881-MONDO_0007034-HP_0000006-GENCC_100001|NOTCH1|Adams-Oliver syndrome|Definitive|Autosomal dominant|Illumina","GENCC_000106-HGNC_7881-OMIM_616028-HP_0000006-GENCC_100002|NOTCH1|Adams-Oliver syndrome 5|Strong|Autosomal dominant|Labcorp Genetics (formerly Invitae)","GENCC_000107-HGNC_7881-OMIM_616028-HP_0000006-GENCC_100001|NOTCH1|Adams-Oliver syndrome 5|Definitive|Autosomal dominant|Laboratory for Molecular Medicine","GENCC_000110-HGNC_7881-ORPHANET_402075-HP_0000006-GENCC_100009|NOTCH1|familial bicuspid aortic valve|Supportive|Autosomal dominant|Orphanet","GENCC_000110-HGNC_7881-ORPHANET_974-HP_0000006-GENCC_100009|NOTCH1|Adams-Oliver syndrome|Supportive|Autosomal dominant|Orphanet","GENCC_000112-HGNC_7881-OMIM_109730-HP_0000006-GENCC_100002|NOTCH1|aortic valve disease 1|Strong|Autosomal dominant|G2P"]}]}