an inherited disorder in which affected individuals have a higher-than-normal chance of developing colorectal cancer and certain other types of cancer, often before the age of 50. also called hereditary nonpolyposis colon cancer and lynch syndrome.
| human | 遺伝子名 | HNPCC |
| 同義語(エイリアス) | DNA mismatch repair protein Msh2; MutS protein homolog 2; COCA1; MSH2; FCC1; HNPCC1 | |
| SWISS-PROTのID | SWISS-PROT:P43246 | |
| EntrezGeneのID | EntrezGene:4436 | |
| その他のDBのID | HGNC:7325 |
| human | 遺伝子名 | HNPCC |
| 同義語(エイリアス) | hMLH1 mismatch repair; MGC5172; COCA2; MLH1; HNPCC2; DNA mismatch repair protein Mlh1; FCC2; MutL protein homolog 1; hMLH1 | |
| SWISS-PROTのID | SWISS-PROT:P40692 | |
| EntrezGeneのID | EntrezGene:4292 | |
| その他のDBのID | HGNC:7127 |
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