{"context":{"query":">>hgnc>>orphanet","source_dataset":"hgnc","target_dataset":"orphanet"},"stats":{"queried":1,"total":2,"mapped":1},"pagination":{"has_next":false},"schema":"id|name|disorder_type|gene_count|phenotype_count","mappings":[{"input":"HGNC:7881","source":"HGNC:7881|notch receptor 1","targets":["402075|Familial bicuspid aortic valve|Morphological anomaly|5|12","974|Adams-Oliver syndrome|Malformation syndrome|6|46"]}]}