All diseases

7 entries on 1 page. Showing entries 1 - 7.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
01221 - Hepatocellular carcinoma 114550 - - - APC, AXIN1, CASP8, CTNNB1, IGF2R, MET, PDGFRL, PIK3CA, TP53 - -
03381 - cancer, gastric (Neoplasm of stomach) 613659 - - - APC, CASP10, ERBB2, FGFR2, IRF1, KLF6, MUTYH, PIK3CA - -
00091 CRC cancer, colorectal (CRC) 114500 - - - AKT1, APC, AURKA, AXIN2, BAX, BUB1B, CCND1, CTNNB1, DCC, DLC1, EP300, FGFR3, FLCN, MCC, MLH3, NRAS, NTHL1, ODC1, PDGFRL, PIK3CA, 7 more - -
00312 FAP-1 adenomatous polyposis, familial, type 1 (FAP-1, Gardner syndrome) 175100 - - - APC - -
00313 HDD desmoid disease, hereditary (HDD) 135290 - - - APC - -
02548 HYPT-1 hypotrichosis, type 1 (HYPT-1) 605389 - - - APCDD1 - -
00314 polyposis polyposis - - - - APC - -
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