3-hydroxyacyl-coa dehydrogenase type 2 deficiency

A family of enzymes that oxidize (S)-3-hydroxyacyl-CoA and NAD+ and produce 3-oxoacyl-CoA, NADH, and H+. These proteins are involved in the metabolism of both fatty acids and amino acids.

Disease Alternative Name

beta--hydroxyacyl coa dehydrogenase
3-keto reductase
l-3-hydroxyacyl coenzyme a dehydrogenase
(s)-3-hydroxyacyl-coa:nad+ oxidoreductase
3-hydroxyacyl coa dehydrogenase
1-specific dpn-linked beta--hydroxybutyric dehydrogenase
3-hydroxybutyryl-coa dehydrogenase
beta--hydroxy acid dehydrogenase
3-hydroxyacyl coenzyme a dehydrogenase
beta--ketoacyl-coa reductase
beta--hydroxyacyl dehydrogenase
3-hydroxyisobutyryl-coa dehydrogenase
3-l-hydroxyacyl-coa dehydrogenase
l-3-hydroxyacyl coa dehydrogenase
3-hydroxyacetyl-coenzyme a dehydrogenase
3-hydroxyacyl-coa dehydrogenase
3beta--hydroxyacyl coenzyme a dehydrogenase
beta--hydroxyacyl-coenzyme a synthetase
beta--hydroxyacylcoenzyme a dehydrogenase
3-hydroxyl-co-a dehydrogenase
beta--hydroxybutyrylcoenzyme a dehydrogenase

Trending Cases