{"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:18618","source":"HGNC:18618|leucine rich repeat kinase 2","targets":["GENCC_000104-HGNC_18618-OMIM_607060-HP_0000006-GENCC_100002|LRRK2|autosomal dominant Parkinson disease 8|Strong|Autosomal dominant|Genomics England PanelApp","GENCC_000106-HGNC_18618-OMIM_607060-HP_0000006-GENCC_100002|LRRK2|autosomal dominant Parkinson disease 8|Strong|Autosomal dominant|Labcorp Genetics (formerly Invitae)","GENCC_000107-HGNC_18618-OMIM_607060-HP_0000006-GENCC_100001|LRRK2|autosomal dominant Parkinson disease 8|Definitive|Autosomal dominant|Laboratory for Molecular Medicine","GENCC_000110-HGNC_18618-ORPHANET_411602-HP_0000006-GENCC_100009|LRRK2|hereditary late onset Parkinson disease|Supportive|Autosomal dominant|Orphanet"]}]}