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E71.510 Zellweger syndrome

BackE71Disorders of branched-chain amino-acid metabolism and fatty-acid metabolism6 →E71.0Maple-syrup-urine diseaseE71.1Other disorders of branched-chain amino-acid metabolism3 →E71.11Branched-chain organic acidurias3 →E71.110Isovaleric acidemiaE71.1113-methylglutaconic aciduriaE71.118Other branched-chain organic aciduriasE71.12Disorders of propionate metabolism3 →E71.120Methylmalonic acidemiaE71.121Propionic acidemiaE71.128Other disorders of propionate metabolismE71.19Other disorders of branched-chain amino-acid metabolismE71.2Disorder of branched-chain amino-acid metabolism, unspecifiedE71.3Disorders of fatty-acid metabolism4 →E71.30Disorder of fatty-acid metabolism, unspecifiedE71.31Disorders of fatty-acid oxidation6 →E71.310Long chain/very long chain acyl CoA dehydrogenase deficiencyE71.311Medium chain acyl CoA dehydrogenase deficiencyE71.312Short chain acyl CoA dehydrogenase deficiencyE71.313Glutaric aciduria type IIE71.314Muscle carnitine palmitoyltransferase deficiencyE71.318Other disorders of fatty-acid oxidationE71.32Disorders of ketone metabolismE71.39Other disorders of fatty-acid metabolismE71.4Disorders of carnitine metabolism5 →E71.40Disorder of carnitine metabolism, unspecifiedE71.41Primary carnitine deficiencyE71.42Carnitine deficiency due to inborn errors of metabolismE71.43Iatrogenic carnitine deficiencyE71.44Other secondary carnitine deficiency2 →E71.440Ruvalcaba-Myhre-Smith syndromeE71.448Other secondary carnitine deficiencyE71.5Peroxisomal disorders5 →E71.50Peroxisomal disorder, unspecifiedE71.51Disorders of peroxisome biogenesis3 →E71.510Zellweger syndromeE71.511Neonatal adrenoleukodystrophyE71.518Other disorders of peroxisome biogenesisE71.52X-linked adrenoleukodystrophy5 →E71.520Childhood cerebral X-linked adrenoleukodystrophyE71.521Adolescent X-linked adrenoleukodystrophyE71.522AdrenomyeloneuropathyE71.528Other X-linked adrenoleukodystrophyE71.529X-linked adrenoleukodystrophy, unspecified typeE71.53Other group 2 peroxisomal disordersE71.54Other peroxisomal disorders4 →E71.540Rhizomelic chondrodysplasia punctataE71.541Zellweger-like syndromeE71.542Other group 3 peroxisomal disordersE71.548Other peroxisomal disorders
CategoryCODABLE
E71.510
Zellweger syndrome
Chapter
IV · Endocrine, nutritional and metabolic diseases
Section
E70-E88
Valid from
Source

CMS ICD-10-CM Tabular List, edition FY2026.