Description of the disease * EnglishPolish Pobierz sekcję do PDF Definition Peroxisomal acyl-CoA oxidase deficiency is a rare neurodegenerative disorder that belongs to the group of inherited peroxisomal disorders and is characterized by hypotonia and seizures in the neonatal period and neurological regression in early infancy. Disease data Classification Disease Synonyms Pseudo-NALD Pseudoadrenoleukodystrofia Pseudo-NALD Pseudo-noworodkowa adrenoleukodystrofia Pseudo-neonatal adrenoleukodystrophy Pseudoadrenoleukodystrophy ORPHA code 2971 OMIM code 264470 ICD10 code E71.3 ICD11 code 5C57.1 *Soruce Extended description of the disease Pobierz sekcję do PDF No additional description. Orphanet - interntowa baza danych dotyczących rzadkich chorób i sierochych leków. ©INSERM 1999 - Dostępna na stronie www.orphanet.pl