All diseases

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

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

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) - - 1464 519 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
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