All diseases

5 entries on 1 page. Showing entries 1 - 5.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00882 cancer, esophageal cancer, esophageal 133239 - 9 1 DCC, DEC1, DLEC1, LZTS1, RNF6, TGFBR2, WWOX - -
05464 HNPCC (Lynch) cancer, colorectal, nonpolyposis, hereditary (Lynch syndrome) - - 1602 629 EPCAM, MLH1, MLH3, MSH2, MSH6, PMS2, TGFBR2 - -
00881 HNPCC6 cancer, colorectal, nonpolyposis, hereditary, type 6 (HNPCC-6) 614331 - - - TGFBR2 - -
00884 LDS Loeys-Dietz syndrome (LDS) - - 54 53 SMAD2, SMAD3, TGFB2, TGFB3, TGFBR1, TGFBR2 - -
00883 LDS2 Loeys-Dietz syndrome, type 2 (LDS-2) 610168 AD 12 11 TGFBR2 - autosomal dominant
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