All diseases

8 entries on 1 page. Showing entries 1 - 8.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
05214 ACC corpus callosum, agenesis ACC 217990 - 23 23 DCC brain -
04653 BBS-16 Bardet-Biedl syndrome, type 16 (BBS-16) 615993 - 0 0 SDCCAG8 - -
00882 cancer, esophageal cancer, esophageal 133239 - 9 1 DCC, DEC1, DLEC1, LZTS1, RNF6, TGFBR2, WWOX - -
00091 CRC cancer, colorectal (CRC) 114500 - 2966 1739 AKT1, APC, AURKA, AXIN2, BAX, BUB1B, CCND1, CTNNB1, DCC, DLC1, EP300, FGFR3, FLCN, MCC, MLH3, NRAS, NTHL1, ODC1, PDGFRL, PIK3CA, 7 more - -
05242 HGPPS2 Horizontal gaze palsy with progressive scoliosis-2 617542 - 3 3 DCC brain;eyes;spine Horizontal gaze palsy, scoliosis, intellectual disability, disorganization of white-matter tracts throughout the human central nervous system, loss of all commissural tracts at multiple levels of the neuraxis occurring with or without congenital mirror movements.
05420 KS Kallmann syndrome - - 146 146 DCC - -
01441 MRMV-1 mirror movements, type 1 (MRMV-1, congenital) 157600 - 60 33 DCC - -
00098 SLSN-7 Senior-Loken syndrome, type 7 (SLSN-7) 613615 - 0 265 SDCCAG8 - -
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