All diseases

3 entries on 1 page. Showing entries 1 - 3.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00513 HNPCC-1;Lynch cancer, colorectal, nonpolyposis, hereditary, type 1 (HNPCC-1, Lynch syndrome) 120435 - - - EPCAM, GALNT12, MLH1, MLH3, MSH2, MSH6, PMS2 - -
00518 HNPCC-4 cancer, colorectal, nonpolyposis, hereditary, type 4 (HNPCC-4) 614337 - - - PMS2 - -
00516 MMRCS cancer syndrome, mismatch repair (MMRCS) 276300 - - - MLH1, MSH2, MSH6, PMS2 - -
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