has material basis in germline mutation in ACOX1 peroxisomal acyl-CoA oxidase deficiency https://github.com/monarch-initiative/mondo/issues/2632 https://www.malacards.org/card/peroxisomal_acyl_coa_oxidase_deficiency pseudo-neonatal adrenoleukodystrophy Pseudoadrenoleukodystrophy ACOX1 deficiency icd11.foundation:927825451 NCIT:C170437 MESH:C536662 SCTID:238069004 MONDO:0009919 Orphanet:2971 pseudo-NALD DOID:0050797 NANDO:1200765 MEDGEN:376636 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. UMLS:C1849678 peroxisomal acyl-CoA oxidase deficiency ICD9:255.41 OMIM:264470 GARD:0004543 disorder of peroxisomal beta oxidation