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
00423 - cancer, endometrial 608089 AD;SMu 226 191 CDH1, MLH3, MSH3, MSH6, PTEN - -
00091 CRC cancer, colorectal, susceptibility to (CRC) 114500 AD;SMu 3065 1838 AKT1, APC, AURKA, AXIN2, BAX, BUB1B, CCND1, CTNNB1, DCC, DLC1, EP300, FGFR3, FLCN, MCC, MLH3, NRAS, NTHL1, ODC1, PDGFRL, PIK3CA, 7 more - -
05464 HNPCC (Lynch) cancer, colorectal, nonpolyposis, hereditary (Lynch syndrome) - - 1602 629 EPCAM, MLH1, MLH3, MSH2, MSH6, PMS2, TGFBR2 - -
00514 HNPCC7 cancer, colorectal, nonpolyposis, hereditary, type 7 (HNPCC-7) 614385 - - - MLH3 - -
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