Disorder of peroxisomal transporter

rare

Any peroxisomal single enzyme/protein defect that disrupts peroxisomal transport.

Subtypes

Disease	ID	Subtypes	Genes
Adrenoleukodystrophy	MONDO:0018544	3	ABCD1
Acyl-CoA binding domain containing protein 5 deficiency	MONDO:0100112		ACBD5
Congenital bile acid synthesis defect 5	MONDO:0014564		ABCD3

Rare disease

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