{"context":{"query":">>hgnc>>gencc","source_dataset":"hgnc","target_dataset":"gencc"},"stats":{"queried":1,"total":4,"mapped":1},"pagination":{"has_next":false},"schema":"id|gene_symbol|disease_title|classification_title|moi_title|submitter_title","mappings":[{"input":"HGNC:20001","source":"HGNC:20001|proprotein convertase subtilisin/kexin type 9","targets":["GENCC_000101-HGNC_20001-MONDO_0011369-HP_0000006-GENCC_100001|PCSK9|hypercholesterolemia, autosomal dominant, 3|Definitive|Autosomal dominant|Ambry Genetics","GENCC_000104-HGNC_20001-OMIM_603776-HP_0000006-GENCC_100002|PCSK9|hypercholesterolemia, autosomal dominant, 3|Strong|Autosomal dominant|Genomics England PanelApp","GENCC_000106-HGNC_20001-OMIM_603776-HP_0000006-GENCC_100002|PCSK9|hypercholesterolemia, autosomal dominant, 3|Strong|Autosomal dominant|Labcorp Genetics (formerly Invitae)","GENCC_000110-HGNC_20001-ORPHANET_391665-HP_0000007-GENCC_100009|PCSK9|homozygous familial hypercholesterolemia|Supportive|Autosomal recessive|Orphanet"]}]}