All diseases

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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
01816 MADD acyl-CoA dehydrogenation deficiency, multiple (MADD) 231680 AR 20 18 ETFA, ETFB, ETFDH - autosomal recessive
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