{"context":{"query":">>hgnc>>gencc","source_dataset":"hgnc","target_dataset":"gencc"},"stats":{"queried":1,"total":9,"mapped":1},"pagination":{"has_next":false},"schema":"id|gene_symbol|disease_title|classification_title|moi_title|submitter_title","mappings":[{"input":"HGNC:11138","source":"HGNC:11138|synuclein alpha","targets":["GENCC_000101-HGNC_11138-MONDO_0005180-HP_0000006-GENCC_100001|SNCA|Parkinson disease|Definitive|Autosomal dominant|Ambry Genetics","GENCC_000101-HGNC_11138-OMIM_605543-HP_0000006-GENCC_100001|SNCA|autosomal dominant Parkinson disease 4|Definitive|Autosomal dominant|Ambry Genetics","GENCC_000104-HGNC_11138-OMIM_127750-HP_0000006-GENCC_100002|SNCA|Lewy body dementia|Strong|Autosomal dominant|Genomics England PanelApp","GENCC_000104-HGNC_11138-OMIM_168601-HP_0000006-GENCC_100002|SNCA|autosomal dominant Parkinson disease 1|Strong|Autosomal dominant|Genomics England PanelApp","GENCC_000104-HGNC_11138-OMIM_605543-HP_0000006-GENCC_100002|SNCA|autosomal dominant Parkinson disease 4|Strong|Autosomal dominant|Genomics England PanelApp","GENCC_000106-HGNC_11138-OMIM_127750-HP_0000006-GENCC_100002|SNCA|Lewy body dementia|Strong|Autosomal dominant|Labcorp Genetics (formerly Invitae)","GENCC_000106-HGNC_11138-OMIM_605543-HP_0000006-GENCC_100002|SNCA|autosomal dominant Parkinson disease 4|Strong|Autosomal dominant|Labcorp Genetics (formerly Invitae)","GENCC_000110-HGNC_11138-ORPHANET_171695-HP_0000007-GENCC_100009|SNCA|parkinsonian-pyramidal syndrome|Supportive|Autosomal recessive|Orphanet","GENCC_000110-HGNC_11138-ORPHANET_411602-HP_0000006-GENCC_100009|SNCA|hereditary late onset Parkinson disease|Supportive|Autosomal dominant|Orphanet"]}]}