{"context":{"query":">>hgnc>>gencc","source_dataset":"hgnc","target_dataset":"gencc"},"stats":{"queried":1,"total":18,"mapped":1},"pagination":{"has_next":false},"schema":"id|gene_symbol|disease_title|classification_title|moi_title|submitter_title","mappings":[{"input":"HGNC:7127","source":"HGNC:7127|mutL homolog 1","targets":["GENCC_000101-HGNC_7127-MONDO_0007254-HP_0000006-GENCC_100005|MLH1|breast cancer|Disputed Evidence|Autosomal dominant|Ambry Genetics","GENCC_000101-HGNC_7127-MONDO_0008315-HP_0000006-GENCC_100004|MLH1|prostate cancer|Limited|Autosomal dominant|Ambry Genetics","GENCC_000101-HGNC_7127-OMIM_158320-HP_0000006-GENCC_100003|MLH1|Muir-Torre syndrome|Moderate|Autosomal dominant|Ambry Genetics","GENCC_000101-HGNC_7127-OMIM_276300-HP_0000007-GENCC_100001|MLH1|mismatch repair cancer syndrome 1|Definitive|Autosomal recessive|Ambry Genetics","GENCC_000101-HGNC_7127-OMIM_609310-HP_0000006-GENCC_100001|MLH1|Lynch syndrome 2|Definitive|Autosomal dominant|Ambry Genetics","GENCC_000104-HGNC_7127-MONDO_0005212-HP_0000007-GENCC_100003|MLH1|rhabdomyosarcoma|Moderate|Autosomal recessive|Genomics England PanelApp","GENCC_000104-HGNC_7127-MONDO_0008170-HP_0000006-GENCC_100002|MLH1|ovarian cancer|Strong|Autosomal dominant|Genomics England PanelApp","GENCC_000104-HGNC_7127-MONDO_0009831-HP_0000006-GENCC_100003|MLH1|malignant pancreatic neoplasm|Moderate|Autosomal dominant|Genomics England PanelApp","GENCC_000104-HGNC_7127-OMIM_158320-HP_0000006-GENCC_100002|MLH1|Muir-Torre syndrome|Strong|Autosomal dominant|Genomics England PanelApp","GENCC_000104-HGNC_7127-OMIM_609310-HP_0000006-GENCC_100002|MLH1|Lynch syndrome 2|Strong|Autosomal dominant|Genomics England PanelApp","GENCC_000106-HGNC_7127-OMIM_120435-HP_0000006-GENCC_100002|MLH1|Lynch syndrome 1|Strong|Autosomal dominant|Labcorp Genetics (formerly Invitae)","GENCC_000106-HGNC_7127-OMIM_276300-HP_0000007-GENCC_100002|MLH1|mismatch repair cancer syndrome 1|Strong|Autosomal recessive|Labcorp Genetics (formerly Invitae)","GENCC_000110-HGNC_7127-ORPHANET_144-HP_0000006-GENCC_100009|MLH1|Lynch syndrome|Supportive|Autosomal dominant|Orphanet","GENCC_000110-HGNC_7127-ORPHANET_252202-HP_0000007-GENCC_100009|MLH1|mismatch repair cancer syndrome 1|Supportive|Autosomal recessive|Orphanet","GENCC_000110-HGNC_7127-ORPHANET_587-HP_0000006-GENCC_100009|MLH1|Muir-Torre syndrome|Supportive|Autosomal dominant|Orphanet","GENCC_000112-HGNC_7127-MONDO_0005835-HP_0000006-GENCC_100001|MLH1|Lynch syndrome|Definitive|Autosomal dominant|G2P","GENCC_000112-HGNC_7127-OMIM_158320-HP_0000006-GENCC_100001|MLH1|Muir-Torre syndrome|Definitive|Autosomal dominant|G2P","GENCC_000112-HGNC_7127-OMIM_276300-HP_0000007-GENCC_100001|MLH1|mismatch repair cancer syndrome 1|Definitive|Autosomal recessive|G2P"]}]}