{"context":{"query":">>hgnc>>orphanet","source_dataset":"hgnc","target_dataset":"orphanet"},"stats":{"queried":1,"total":1,"mapped":1},"pagination":{"has_next":false},"schema":"id|name|disorder_type|gene_count|phenotype_count","mappings":[{"input":"HGNC:20001","source":"HGNC:20001|proprotein convertase subtilisin/kexin type 9","targets":["391665|Homozygous familial hypercholesterolemia|Disease|6|33"]}]}