{"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:7029","source":"HGNC:7029|MET proto-oncogene, receptor tyrosine kinase","targets":["319298|Papillary renal cell carcinoma|Disease|2|0","33402|Pediatric hepatocellular carcinoma|Disease|2|9","47044|Hereditary papillary renal cell carcinoma|Disease|1|0","488265|Osteofibrous dysplasia|Disease|1|0","90636|Rare autosomal recessive non-syndromic sensorineural deafness type DFNB|Etiological subtype|74|0"]}]}