{"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:7765","source":"HGNC:7765|neurofibromin 1","targets":["GENCC_000102-HGNC_7765-MONDO_0016248-HP_0000005-GENCC_100008|NF1|familial ovarian cancer|No Known Disease Relationship|Unknown|ClinGen","GENCC_000104-HGNC_7765-MONDO_0016820-HP_0000006-GENCC_100003|NF1|Moyamoya disease|Moderate|Autosomal dominant|Genomics England PanelApp","GENCC_000104-HGNC_7765-OMIM_162200-HP_0000006-GENCC_100002|NF1|neurofibromatosis type 1|Strong|Autosomal dominant|Genomics England PanelApp","GENCC_000104-HGNC_7765-OMIM_601321-HP_0000006-GENCC_100002|NF1|neurofibromatosis-Noonan syndrome|Strong|Autosomal dominant|Genomics England PanelApp","GENCC_000106-HGNC_7765-OMIM_162200-HP_0000006-GENCC_100002|NF1|neurofibromatosis type 1|Strong|Autosomal dominant|Labcorp Genetics (formerly Invitae)","GENCC_000110-HGNC_7765-ORPHANET_29072-HP_0000006-GENCC_100009|NF1|hereditary pheochromocytoma-paraganglioma|Supportive|Autosomal dominant|Orphanet","GENCC_000110-HGNC_7765-ORPHANET_638-HP_0000006-GENCC_100009|NF1|neurofibromatosis-Noonan syndrome|Supportive|Autosomal dominant|Orphanet","GENCC_000112-HGNC_7765-OMIM_162200-HP_0000006-GENCC_100001|NF1|neurofibromatosis type 1|Definitive|Autosomal dominant|G2P"]}]}