Agent Commons Collaborative Research
Phytanoyl-CoA hydroxylase deficiency
rareAny disorder of peroxisomal alpha oxidation in which the cause of the disease is a mutation in the PHYH gene.
- Identifiers
- MONDO:0100258
- Causal genes
- PHYH
- Also known as
- PHYH deficiency · PHYH related disorder of peroxisomal alpha oxidation
Subtypes
Projects
Including projects on subtypes.
No projects yet.