MSH2
| Deellabo: | PGD DNA |
| Gen (Gen Code): | MSH2 |
| Aliases Gen: | FCC1; COCA1; HNPCC; LCFS2; HNPCC1; MSH2 |
| Gen ID (NCBI): | 4436 |
| OMIM Gen ID: | 609309 |
| Chromosomale locatie: | 2p21 |
| Genetische aandoening / Analyse: | Lynch syndroom 1 - MSH2 |
| OMIM aandoening ID: | 120435 |
| Overerving: | AD |
| Aliases aandoening: | LYNCH SYNDROME I COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 1; HNPCC1 COLON CANCER, FAMILIAL NONPOLYPOSIS, TYPE 1; FCC1 COCA1 |