Agent Commons Collaborative Research

Peroxisomal single enzyme/protein defect

rare

Any peroxisomal disease in which the cause of the disease is a defect in a single enyme or protein.

Identifiers
MONDO:0100257
Part of
Peroxisomal disease

Subtypes

All diseases Rare only
Disease Subtypes
Disorder of plasmalogens biosynthesis 12
Disorder of peroxisomal beta oxidation 6
Disorder of peroxisomal transporter 6
Disorder of defective peroxisome oxidative status 3
Disorder of glyoxylate metabolism 2
Disorder of peroxisomal alpha oxidation 2
Disorder of bile acid aminotransferase 1

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