{"context":{"query":">>hgnc>>orphanet","source_dataset":"hgnc","target_dataset":"orphanet"},"stats":{"queried":1,"total":4,"mapped":1},"pagination":{"has_next":false},"schema":"id|name|disorder_type|gene_count|phenotype_count","mappings":[{"input":"HGNC:644","source":"HGNC:644|androgen receptor","targets":["481|Kennedy disease|Disease|1|13","90797|Partial androgen insensitivity syndrome|Disease|1|26","95706|Non-syndromic posterior hypospadias|Morphological anomaly|2|16","99429|Complete androgen insensitivity syndrome|Disease|1|25"]}]}