{"context":{"query":">>hgnc>>orphanet","source_dataset":"hgnc","target_dataset":"orphanet"},"stats":{"queried":1,"total":1,"mapped":1},"pagination":{"has_next":false},"schema":"id|name|disorder_type|gene_count|phenotype_count","mappings":[{"input":"HGNC:12559","source":"HGNC:12559|uromodulin","targets":["88950|UMOD-related autosomal dominant tubulointerstitial kidney disease|Clinical subtype|1|0"]}]}