5C57.1
category
Disorders of peroxisomal alpha-, beta- or omega-oxidation
Also indexed as
AdrenomyeloneuropathyBifunctional enzyme deficiencyDisorders of peroxisomal alpha-, beta- or omega-oxidationHMSN 4 - [Hereditary motor and sensory neuropathy type 4]Hereditary motor and sensory neuropathy type 4Heredoataxia hemeralopica polyneuritiformisInfantile Refsum diseasePeroxisomal D-bifunctional enzyme deficiencyPeroxisomal acyl-CoA oxidase deficiencyPhytanic acid oxidase deficiencyPhytanic acid storage diseasePseudo-neonatal adrenoleukodystrophyPseudoadrenoleukodystrophyRefsum diseaseRefsum-Thiebaut diseaseSchilder-Addison complexSterol carrier protein deficiencyX-linked adrenoleukodystrophyX-linked adult-onset adrenomyeloneuropathyX-linked cerebral adrenoleukodystrophyX-linked childhood adrenoleukodystrophy