All diseases

1 entry on 1 page. Showing entry 1.

ID     

AscendingAbbreviation     

Name     

OMIM ID     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00001 Lynch Syndrome cancer, colorectal, nonpolyposis, hereditary, type 1 (Lynch syndrome, HNPCC-1) 120435 1367 429 MLH1, MLH3, MSH2, MSH3, MSH6, PMS2 - -