{"context":{"query":">>hgnc>>gencc","source_dataset":"hgnc","target_dataset":"gencc"},"stats":{"queried":1,"total":16,"mapped":1},"pagination":{"has_next":false},"schema":"id|gene_symbol|disease_title|classification_title|moi_title|submitter_title","mappings":[{"input":"HGNC:4177","source":"HGNC:4177|glucosylceramidase beta 1","targets":["GENCC_000101-HGNC_4177-OMIM_168600-HP_0000006-GENCC_100002|GBA1|late-onset Parkinson disease|Strong|Autosomal dominant|Ambry Genetics","GENCC_000104-HGNC_4177-OMIM_168600-HP_0000006-GENCC_100002|GBA1|late-onset Parkinson disease|Strong|Autosomal dominant|Genomics England PanelApp","GENCC_000104-HGNC_4177-OMIM_230800-HP_0000007-GENCC_100002|GBA1|Gaucher disease type I|Strong|Autosomal recessive|Genomics England PanelApp","GENCC_000104-HGNC_4177-OMIM_230900-HP_0000007-GENCC_100002|GBA1|Gaucher disease type II|Strong|Autosomal recessive|Genomics England PanelApp","GENCC_000104-HGNC_4177-OMIM_231000-HP_0000007-GENCC_100002|GBA1|Gaucher disease type III|Strong|Autosomal recessive|Genomics England PanelApp","GENCC_000104-HGNC_4177-OMIM_231005-HP_0000007-GENCC_100002|GBA1|Gaucher disease-ophthalmoplegia-cardiovascular calcification syndrome|Strong|Autosomal recessive|Genomics England PanelApp","GENCC_000104-HGNC_4177-OMIM_608013-HP_0000007-GENCC_100002|GBA1|Gaucher disease perinatal lethal|Strong|Autosomal recessive|Genomics England PanelApp","GENCC_000106-HGNC_4177-OMIM_168600-HP_0000006-GENCC_100004|GBA1|late-onset Parkinson disease|Limited|Autosomal dominant|Labcorp Genetics (formerly Invitae)","GENCC_000106-HGNC_4177-OMIM_230800-HP_0000007-GENCC_100002|GBA1|Gaucher disease type I|Strong|Autosomal recessive|Labcorp Genetics (formerly Invitae)","GENCC_000107-HGNC_4177-OMIM_608013-HP_0000007-GENCC_100001|GBA1|Gaucher disease perinatal lethal|Definitive|Autosomal recessive|Laboratory for Molecular Medicine","GENCC_000108-HGNC_4177-MONDO_0018150-HP_0000007-GENCC_100001|GBA1|Gaucher disease|Definitive|Autosomal recessive|Myriad Women’s Health","GENCC_000110-HGNC_4177-ORPHANET_2072-HP_0000007-GENCC_100009|GBA1|Gaucher disease-ophthalmoplegia-cardiovascular calcification syndrome|Supportive|Autosomal recessive|Orphanet","GENCC_000110-HGNC_4177-ORPHANET_77259-HP_0000007-GENCC_100009|GBA1|Gaucher disease type I|Supportive|Autosomal recessive|Orphanet","GENCC_000110-HGNC_4177-ORPHANET_77260-HP_0000007-GENCC_100009|GBA1|Gaucher disease type II|Supportive|Autosomal recessive|Orphanet","GENCC_000110-HGNC_4177-ORPHANET_77261-HP_0000007-GENCC_100009|GBA1|Gaucher disease type III|Supportive|Autosomal recessive|Orphanet","GENCC_000112-HGNC_4177-OMIM_608013-HP_0000007-GENCC_100001|GBA1|Gaucher disease perinatal lethal|Definitive|Autosomal recessive|G2P"]}]}