{"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:2505","source":"HGNC:2505|cytotoxic T-lymphocyte associated protein 4","targets":["GENCC_000101-HGNC_2505-OMIM_616100-HP_0000006-GENCC_100002|CTLA4|autoimmune lymphoproliferative syndrome due to CTLA4 haploinsufficiency|Strong|Autosomal dominant|Ambry Genetics","GENCC_000106-HGNC_2505-OMIM_616100-HP_0000006-GENCC_100002|CTLA4|autoimmune lymphoproliferative syndrome due to CTLA4 haploinsufficiency|Strong|Autosomal dominant|Labcorp Genetics (formerly Invitae)","GENCC_000110-HGNC_2505-ORPHANET_436159-HP_0000006-GENCC_100009|CTLA4|autoimmune lymphoproliferative syndrome due to CTLA4 haploinsufficiency|Supportive|Autosomal dominant|Orphanet","GENCC_000110-HGNC_2505-ORPHANET_536-HP_0000005-GENCC_100009|CTLA4|systemic lupus erythematosus|Supportive|Unknown|Orphanet"]}]}