disease caused by disruption of disease has basis in disruption of peroxisome inborn errors of metabolism peroxisomal disease A group of congenital disorders of lipid metabolism, caused by loss of the normal peroxisomes. Signs and symptoms include developmental delays, mental retardation, facial abnormalities, hepatomegaly, and hypotonia. COHD:441268 DOID:906 ICD10:E71.5 ICD10:E71.50 ICD9:277.86 ICD9:277.89 MONDO:0019053 NCIT:C85005 Orphanet:68373 SCTID:238059005 UMLS:C0282528 disorder of peroxisomal function peroxisomal disorder peroxisomal function disorder genetic nervous system disorder metabolic epilepsy