All diseases

4 entries on 1 page. Showing entries 1 - 4.

ID     

AscendingAbbreviation     

Name     

OMIM ID     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
03286 DIAR-5 diarrhea, type 5, with tufting enteropathy, congenital (DIAR-5) 613217 1 1 EPCAM - autosomal recessive
05464 HNPCC cancer, colorectal, nonpolyposis, hereditary (HNPCC, Lynch syndrome) - 1443 498 EPCAM, MLH1, MLH3, MSH2, MSH6, PMS2, TGFBR2 - -
00513 HNPCC-1 (Lynch) cancer, colorectal, nonpolyposis, hereditary, type 1 (HNPCC-1, Lynch syndrome) 120435 8 7 EPCAM, GALNT12, MLH1, MLH3, MSH2, MSH6, PMS2 - -
00520 HNPCC-8 cancer, colorectal, nonpolyposis, hereditary, type 8 (HNPCC-8) 613244 70 70 EPCAM - autosomal dominant