EHHADH

EHHADH is a human gene that encodes for a bifunctional enzyme and is one of the four enzymes of the peroxisomal beta-oxidation pathway. Mutations of the gene are a cause of peroxisomal disorders such as Zellweger syndrome. ^[1]

enoyl-CoA, hydratase/3-hydroxyacyl CoA dehydrogenase
Identifiers
Symbol	EHHADH
Alt. symbols	ECHD
NCBI gene	1962
HGNC	3247
OMIM	607037
Other data
EC number	4.2.1.17
Locus	Chr. 3 q26.3-q28

See also

• HSD17B4