{"context":{"query":">>hgnc>>orphanet","source_dataset":"hgnc","target_dataset":"orphanet"},"stats":{"queried":1,"total":5,"mapped":1},"pagination":{"has_next":false},"schema":"id|name|disorder_type|gene_count|phenotype_count","mappings":[{"input":"HGNC:9884","source":"HGNC:9884|RB transcriptional corepressor 1","targets":["1587|Monosomy 13q14 syndrome|Malformation syndrome|1|30","357027|Hereditary retinoblastoma|Clinical subtype|2|0","357034|Non-hereditary retinoblastoma|Clinical subtype|2|0","668|Osteosarcoma|Disease|4|12","70573|Small cell lung cancer|Disease|3|0"]}]}