All ICD10 Codes
Chapter 4

E00–E89: Endocrine, Nutritional and Metabolic Diseases

Endocrine, Nutritional and Metabolic Diseases diagnostic classification updated for 2026.

Chapter Instructions

Excludes1(Not coded here. Use a different code.)
  • transitory endocrine and metabolic disorders specific to newborn (P70-P74)
All CodesBillable Only
Internal Codes
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  • E71.510—

    Zellweger syndrome

  • E71.511—

    Neonatal adrenoleukodystrophy

  • 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

  • E71.529—

    X-linked adrenoleukodystrophy, unspecified type

  • E71.53—

    Other group 2 peroxisomal disorders

  • E71.54—

    Other peroxisomal disorders

  • E71.540—

    Rhizomelic chondrodysplasia punctata

  • E71.541—

    Zellweger-like syndrome

  • E71.542—

    Other group 3 peroxisomal disorders

  • E71.548—

    Other peroxisomal disorders

  • E72—

    Other disorders of amino-acid metabolism

  • E72.0—

    Disorders of amino-acid transport

  • E72.00—

    Disorders of amino-acid transport, unspecified

  • E72.01—

    Cystinuria

  • E72.02—

    Hartnup's disease

  • E72.03—

    Lowe's syndrome

  • E72.04—

    Cystinosis

  • E72.09—

    Other disorders of amino-acid transport

  • E72.1—

    Disorders of sulfur-bearing amino-acid metabolism

  • E72.10—

    Disorders of sulfur-bearing amino-acid metabolism, unspecified

  • E72.11—

    Homocystinuria

  • E72.12—

    Methylenetetrahydrofolate reductase deficiency

  • E72.19—

    Other disorders of sulfur-bearing amino-acid metabolism

  • E72.2—

    Disorders of urea cycle metabolism

  • E72.20—

    Disorder of urea cycle metabolism, unspecified

  • E72.21—

    Argininemia

  • E72.22—

    Arginosuccinic aciduria

  • E72.23—

    Citrullinemia

  • E72.29—

    Other disorders of urea cycle metabolism

  • E72.3—

    Disorders of lysine and hydroxylysine metabolism

  • E72.4—

    Disorders of ornithine metabolism

  • E72.5—

    Disorders of glycine metabolism

  • E72.50—

    Disorder of glycine metabolism, unspecified

  • E72.51—

    Non-ketotic hyperglycinemia

  • E72.52—

    Trimethylaminuria

  • E72.53—

    Primary hyperoxaluria

  • E72.530—

    Primary hyperoxaluria, type 1

  • E72.538—

    Other specified primary hyperoxaluria

  • E72.539—

    Primary hyperoxaluria, unspecified

  • E72.54—

    Secondary hyperoxaluria

  • E72.540—

    Dietary hyperoxaluria

  • E72.541—

    Enteric hyperoxaluria

  • E72.548—

    Other secondary hyperoxaluria

  • E72.549—

    Secondary hyperoxaluria, unspecified

  • E72.59—

    Other disorders of glycine metabolism

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