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5C57.1 Disorders of peroxisomal alpha-, beta- or omega-oxidation

International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2024-01

code elsewhere

• Congenital bile acid synthesis defect type 4  (5C52.11)

synonyms

• Disorders of peroxisomal alpha-, beta- or omega-oxidation
• Refsum disease
• Hereditary motor and sensory neuropathy type 4
• Phytanic acid oxidase deficiency
• Phytanic acid storage disease
• Heredoataxia hemeralopica polyneuritiformis
• Refsum-Thiebaut disease
• HMSN 4 - [Hereditary motor and sensory neuropathy type 4]
• Infantile Refsum disease
• X-linked adrenoleukodystrophy
• Schilder-Addison complex
• X-linked cerebral adrenoleukodystrophy
• X-linked childhood adrenoleukodystrophy
• Adrenomyeloneuropathy
• X-linked adult-onset adrenomyeloneuropathy
• Peroxisomal D-bifunctional enzyme deficiency
• Bifunctional enzyme deficiency
• Peroxisomal acyl-CoA oxidase deficiency
• Pseudo-neonatal adrenoleukodystrophy
• Pseudoadrenoleukodystrophy
• Sterol carrier protein deficiency

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