| 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 |
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]