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51 Disorders of peroxisome biogenesis
- Group 1 peroxisomal disorders
- Excludes1: Refsum's disease (G60.1)
- E71.510 Zellweger syndrome
- E71.511 Neonatal adrenoleukodystrophy
- Excludes1: X-linked adrenoleukodystrophy (E71.42-)
- E71.518 Other disorders of peroxisome biogenesis
- E71.52 X-linked adrenoleukodystrophy
- E71.520 Childhood cerebral X-linked adrenoleukodystrophy
- E71.521 Adolescent X-linked adrenoleukodystrophy
- E71.522 Adrenomyeloneuropathy
- E71.528 Other X-linked adrenoleukodystrophy
- Addison only phenotype adrenoleukodystrophy
- Addison-Schilder adrenoleukodystrophy
- E71.529 X-linked adrenoleukodystrophy, unspecified
- E71.53 Other group 2 peroxisomal disorders
- E71.54 Other peroxisomal disorders
- E71.540 Rhizomelic chondrodysplasia punctata
- Excludes1: chondrodysplasia punctata NOS (Q77.3)
- E71.541 Zellweger-like syndrome
- E71.542 Other group 3 peroxisomal disorders
- E71.548 Other peroxisomal disorders
- E71.540 Rhizomelic chondrodysplasia punctata
E72 Other disorders of amino-acid metabolism
- Excludes1: disorders of:
- aromatic amino-acid metabolism (E70.-)
- branched-chain amino-acid metabolism (E71.0-E71.2)
- fatty-acid metabolism (E71.3)
- purine and pyrimidine metabolism (E79.-)
- gout ( M1a-, M10.-)
- E72.0 Disorders of amino-acid transport
- Excludes1: disorders of tryptophan metabolism (E70.5)
- E72.00 Disorders of amino-acid transport, unspecified
- E72.01 Cystinuria
- E72.02 Hartnup's disease
- E72.03 Lowe's syndrome
- Use additional code for associated glaucoma (H42)
- E72.04 Cystinosis
- Fanconi (-de Toni) (-Debr?) syndrome with cystinosis
- Excludes1: Fanconi (-de Toni) (-Debr?) syndrome without cystinosis (E72.09)
- E72.09 Other disorders of amino-acid transport
- Fanconi (-de Toni) (-Debr?) syndrome, unspecified
- E72.
