{"context":{"query":">>hgnc>>gencc","source_dataset":"hgnc","target_dataset":"gencc"},"stats":{"queried":1,"total":6,"mapped":1},"pagination":{"has_next":false},"schema":"id|gene_symbol|disease_title|classification_title|moi_title|submitter_title","mappings":[{"input":"HGNC:1884","source":"HGNC:1884|CF transmembrane conductance regulator","targets":["GENCC_000106-HGNC_1884-OMIM_167800-HP_0000006-GENCC_100004|CFTR|hereditary chronic pancreatitis|Limited|Autosomal dominant|Labcorp Genetics (formerly Invitae)","GENCC_000106-HGNC_1884-OMIM_219700-HP_0000007-GENCC_100002|CFTR|cystic fibrosis|Strong|Autosomal recessive|Labcorp Genetics (formerly Invitae)","GENCC_000107-HGNC_1884-OMIM_219700-HP_0000007-GENCC_100001|CFTR|cystic fibrosis|Definitive|Autosomal recessive|Laboratory for Molecular Medicine","GENCC_000108-HGNC_1884-MONDO_0009061-HP_0000007-GENCC_100001|CFTR|cystic fibrosis|Definitive|Autosomal recessive|Myriad Women’s Health","GENCC_000110-HGNC_1884-ORPHANET_48-HP_0000007-GENCC_100009|CFTR|congenital bilateral absence of vas deferens|Supportive|Autosomal recessive|Orphanet","GENCC_000110-HGNC_1884-ORPHANET_586-HP_0000007-GENCC_100009|CFTR|cystic fibrosis|Supportive|Autosomal recessive|Orphanet"]}]}