{"context":{"query":">>hgnc>>gencc","source_dataset":"hgnc","target_dataset":"gencc"},"stats":{"queried":1,"total":8,"mapped":1},"pagination":{"has_next":false},"schema":"id|gene_symbol|disease_title|classification_title|moi_title|submitter_title","mappings":[{"input":"HGNC:6893","source":"HGNC:6893|microtubule associated protein tau","targets":["GENCC_000104-HGNC_6893-OMIM_168600-HP_0000006-GENCC_100002|MAPT|late-onset Parkinson disease|Strong|Autosomal dominant|Genomics England PanelApp","GENCC_000104-HGNC_6893-OMIM_172700-HP_0000006-GENCC_100002|MAPT|Pick disease|Strong|Autosomal dominant|Genomics England PanelApp","GENCC_000104-HGNC_6893-OMIM_260540-HP_0000007-GENCC_100003|MAPT|progressive supranuclear palsy-parkinsonism syndrome|Moderate|Autosomal recessive|Genomics England PanelApp","GENCC_000104-HGNC_6893-OMIM_600274-HP_0000006-GENCC_100002|MAPT|semantic dementia|Strong|Autosomal dominant|Genomics England PanelApp","GENCC_000104-HGNC_6893-OMIM_601104-HP_0000006-GENCC_100002|MAPT|supranuclear palsy, progressive, 1|Strong|Autosomal dominant|Genomics England PanelApp","GENCC_000106-HGNC_6893-OMIM_168600-HP_0000005-GENCC_100004|MAPT|late-onset Parkinson disease|Limited|Unknown|Labcorp Genetics (formerly Invitae)","GENCC_000106-HGNC_6893-OMIM_172700-HP_0000006-GENCC_100002|MAPT|Pick disease|Strong|Autosomal dominant|Labcorp Genetics (formerly Invitae)","GENCC_000106-HGNC_6893-OMIM_260540-HP_0000007-GENCC_100004|MAPT|progressive supranuclear palsy-parkinsonism syndrome|Limited|Autosomal recessive|Labcorp Genetics (formerly Invitae)"]}]}