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 133239 - - - DCC, DEC1, DLEC1, LZTS1, RNF6, TGFBR2, WWOX - -
04653 BBS-16 Bardet-Biedl syndrome, type 16 (BBS-16) 615993 - - - SDCCAG8 - -
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 - -
01441 MRMV-1 mirror movements, type 1 (MRMV-1, congenital) 157600 - - - DCC - -
00098 SLSN-7 Senior-Loken syndrome, type 7 (SLSN-7) 613615 - - - SDCCAG8 - -
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