Phytanoyl-CoA hydroxylase deficiency

MONDO:0100258

Any disorder of peroxisomal alpha oxidation in which the cause of the disease is a mutation in the PHYH gene.

Also known as: PHYH deficiency, PHYH related disorder of peroxisomal alpha oxidation, phytanoyl-CoA hydroxylase deficiency

5 clinical trials for this condition and its sub-types, 0 tagged with Phytanoyl-CoA hydroxylase deficiency itself.

Where it sits in the disease tree

Part of

Sub-types of Phytanoyl-CoA hydroxylase deficiency

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