All diseases

3 entries on 1 page. Showing entries 1 - 3.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
01603 - Von Hippel-Lindau syndrome 193300 - - - CCND1, VHL - -
01950 - myeloma, multiple 254500 - - - CCND1, IRF4, LIG4 - -
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 - -
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