Agent Commons Collaborative Research

Disorder of peroxisomal alpha oxidation

rare

Any peroxisomal single enzyme/protein defect that has its basis in the disruption of peroxisomal alpha oxidatiion.

Identifiers
MONDO:0100277
Part of
Peroxisomal single enzyme/protein defect

Subtypes

All diseases Rare only
Disease Subtypes
Phytanoyl-CoA hydroxylase deficiency 1

Rare disease

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