{"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:7127","source":"HGNC:7127|mutL homolog 1","targets":["144|Lynch syndrome|Disease|9|62","252202|Constitutional mismatch repair deficiency syndrome|Disease|4|0"]}]}