Page:ICD-10-CM (2010).djvu/214

 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

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.