E71.54 Other peroxisomal disorders

Non-billable header with 4 child codes.

Applies from E71.5 Peroxisomal disorders

Excludes1 (never code together)

• Schilder's disease (G37.0)

Codes under E71.54

• E71.540 Rhizomelic chondrodysplasia punctata
• E71.541 Zellweger-like syndrome
• E71.542 Other group 3 peroxisomal disorders
• E71.548 Other peroxisomal disorders

Code annotations containing back-references to E71.54

Back-references to E71.5

• Type 1 Excludes: E71.3 Disorders of fatty-acid metabolism ("peroxisomal disorders (E71.5)")

Back-references to E71

• Type 2 Excludes: G11 Hereditary ataxia ("metabolic disorders (E70-E88)")
• Code First: G63 Polyneuropathy in diseases classified elsewhere ("metabolic diseases (E70-E88)")
• Type 2 Excludes: G71 Primary disorders of muscles ("metabolic disorders (E70-E88)")
• Code First: H42 Glaucoma in diseases classified elsewhere ("specified metabolic disorder (E70-E88)")
• Type 2 Excludes: N25.0 Renal osteodystrophy ("metabolic disorders classifiable to E70-E88")
• Type 2 Excludes: N25.81 Secondary hyperparathyroidism of renal origin ("metabolic disorders classifiable to E70-E88")
• Type 1 Excludes: P59 Neonatal jaundice from other and unspecified causes ("jaundice due to inborn errors of metabolism (E70-E88)")
• Type 1 Excludes: R79 Other abnormal findings of blood chemistry ("specific findings indicating disorder of amino-acid metabolism (E70-E72)")
• Type 1 Excludes: R79.83 Abnormal findings of blood amino-acid level ("disorders of amino-acid metabolism (E70-E72)")

Nearby codes

• E71.521 Adolescent X-linked adrenoleukodystrophy
• E71.522 Adrenomyeloneuropathy
• E71.528 Other X-linked adrenoleukodystrophy
• E71.529 X-linked adrenoleukodystrophy, unspecified type
• E71.53 Other group 2 peroxisomal disorders
• E71.54 Other peroxisomal disorders (this code)
• E71.540 Rhizomelic chondrodysplasia punctata
• E71.541 Zellweger-like syndrome
• E71.542 Other group 3 peroxisomal disorders
• E71.548 Other peroxisomal disorders