Disease #00016 (MADD (Multiple acyl-CoA dehydrogenase deﬁciency), OMIM:231680)

Zhejiang University Center for Genetic and Genomic Medicine (ZJU-CGGM)

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Official abbreviation	MADD
Name	Multiple acyl-CoA dehydrogenase deﬁciency
OMIM ID	231680
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 3 genes	ETFA, ETFB, ETFDH
Associated tissues	liver
Disease features	-
Remarks	-