5C57.1
Disorders of peroxisomal alpha-, beta- or omega-oxidation
Distúrbios da oxidação peroxissômica alfa, beta ou ômega
CategoryIndex Terms
Disorders of peroxisomal alpha-, beta- or omega-oxidationRefsum diseaseHereditary motor and sensory neuropathy type 4Phytanic acid oxidase deficiencyPhytanic acid storage diseaseHeredoataxia hemeralopica polyneuritiformisRefsum-Thiebaut diseaseHMSN 4 - [Hereditary motor and sensory neuropathy type 4]Infantile Refsum diseaseX-linked adrenoleukodystrophySchilder-Addison complexX-linked cerebral adrenoleukodystrophyX-linked childhood adrenoleukodystrophyAdrenomyeloneuropathyX-linked adult-onset adrenomyeloneuropathyPeroxisomal D-bifunctional enzyme deficiencyBifunctional enzyme deficiencyPeroxisomal acyl-CoA oxidase deficiencyPseudo-neonatal adrenoleukodystrophyPseudoadrenoleukodystrophySterol carrier protein deficiency