{"context":{"query":">>hgnc>>orphanet","source_dataset":"hgnc","target_dataset":"orphanet"},"stats":{"queried":1,"total":3,"mapped":1},"pagination":{"has_next":false},"schema":"id|name|disorder_type|gene_count|phenotype_count","mappings":[{"input":"HGNC:11766","source":"HGNC:11766|transforming growth factor beta 1","targets":["1328|Camurati-Engelmann disease|Malformation syndrome|1|54","565788|Infantile inflammatory bowel disease with neurological involvement|Disease|1|0","586|Cystic fibrosis|Disease|19|35"]}]}