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
00882 cancer, esophageal cancer, esophageal 133239 - 9 1 DCC, DEC1, DLEC1, LZTS1, RNF6, TGFBR2, WWOX - -
05065 EIEE-28 encephalopathy, epileptic, early infantile, type 28 (EIEE-28) 616211 - 2 2 WWOX - -
05066 SCAR-12 ataxia, spinocerebellar, autosomal recessive, type 12 (SCAR12) 614322 - 0 0 WWOX - -
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