All diseases

1 entry on 1 page. Showing entry 1.

ID     

AscendingAbbreviation     

Name     

OMIM ID     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
01816 MADD acyl-CoA dehydrogenation deficiency, multiple (MADD) 231680 11 11 ETFA, ETFB, ETFDH - autosomal recessive