All diseases

2 entries on 1 page. Showing entries 1 - 2.

ID     

AscendingAbbreviation     

Name     

OMIM ID     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00016 252011 Mitochondrial complex II deficiency, 252011 (3) 252011 0 0 SDHA, SDHAF1, SDHD - -
00086 CMD1GG Cardiomyopathy, dilated, 1GG, 613642 (3) 613642 0 0 SDHA - -