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)
Internal Codes
  • E78.1|

    Pure hyperglyceridemia

  • E78.2|

    Mixed hyperlipidemia

  • E78.3|

    Hyperchylomicronemia

  • E78.4|

    Other hyperlipidemia

  • E78.41|

    Elevated Lipoprotein(a)

  • E78.49|

    Other hyperlipidemia

  • E78.5|

    Hyperlipidemia, unspecified

  • E78.6|

    Lipoprotein deficiency

  • E78.7|

    Disorders of bile acid and cholesterol metabolism

  • E78.70|

    Disorder of bile acid and cholesterol metabolism, unspecified

  • E78.71|

    Barth syndrome

  • E78.72|

    Smith-Lemli-Opitz syndrome

  • E78.79|

    Other disorders of bile acid and cholesterol metabolism

  • E78.8|

    Other disorders of lipoprotein metabolism

  • E78.81|

    Lipoid dermatoarthritis

  • E78.89|

    Other lipoprotein metabolism disorders

  • E78.9|

    Disorder of lipoprotein metabolism, unspecified

  • E79|

    Disorders of purine and pyrimidine metabolism

  • E79.0|

    Hyperuricemia without signs of inflammatory arthritis and tophaceous disease

  • E79.1|

    Lesch-Nyhan syndrome

  • E79.2|

    Myoadenylate deaminase deficiency

  • E79.8|

    Other disorders of purine and pyrimidine metabolism

  • E79.81|

    Aicardi-Goutières syndrome

  • E79.82|

    Hereditary xanthinuria

  • E79.89|

    Other specified disorders of purine and pyrimidine metabolism

  • E79.9|

    Disorder of purine and pyrimidine metabolism, unspecified

  • E80|

    Disorders of porphyrin and bilirubin metabolism

  • E80.0|

    Hereditary erythropoietic porphyria

  • E80.1|

    Porphyria cutanea tarda

  • E80.2|

    Other and unspecified porphyria

  • E80.20|

    Unspecified porphyria

  • E80.21|

    Acute intermittent (hepatic) porphyria

  • E80.29|

    Other porphyria

  • E80.3|

    Defects of catalase and peroxidase

  • E80.4|

    Gilbert syndrome

  • E80.5|

    Crigler-Najjar syndrome

  • E80.6|

    Other disorders of bilirubin metabolism

  • E80.7|

    Disorder of bilirubin metabolism, unspecified

  • E83|

    Disorders of mineral metabolism

  • E83.0|

    Disorders of copper metabolism

  • E83.00|

    Disorder of copper metabolism, unspecified

  • E83.01|

    Wilson's disease

  • E83.09|

    Other disorders of copper metabolism

  • E83.1|

    Disorders of iron metabolism

  • E83.10|

    Disorder of iron metabolism, unspecified

  • E83.11|

    Hemochromatosis

  • E83.110|

    Hereditary hemochromatosis

  • E83.111|

    Hemochromatosis due to repeated red blood cell transfusions

  • E83.118|

    Other hemochromatosis

  • E83.119|

    Hemochromatosis, unspecified

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