ICD-11 classes
05 Endocrine, nutritional or metabolic diseases
Metabolic disorders
5C90 — Metabolic or transporter liver disease

ICD-11 5C90 — Metabolic or transporter liver disease

The diagnosis has no description.

The diagnosis includes nothing.

It excludes 4 items.

  • Alcoholic liver disease (DB94)
  • Non-alcoholic fatty liver disease (DB92)
  • Drug-induced or toxic liver disease (DB95)
  • Acute fatty liver of pregnancy (JA65.0)

Diagnosis with code 5C90 contains 16 clarifying diagnoses:

  1. 5C90.0 — Liver diseases due to urea cycle defects
    It contains 3 clarifying diagnoses.
  2. 5C90.1 — Liver diseases due to disorders of porphyrin or bilirubin metabolism or transport
    It contains 5 clarifying diagnoses.
  3. 5C90.2 — Liver diseases due to disorders of amino acid metabolism
    It contains 2 clarifying diagnoses.
  4. 5C90.3 — Liver disease due to disorders of lysosomal storage
  5. 5C90.4 — Liver diseases due to mitochondrial disorders
  6. 5C90.5 — Liver diseases due to disorders of mineral metabolism
    It contains 1 clarifying diagnosis.
  7. 5C52.11 — Bile acid synthesis defect with cholestasis
  8. 5C58.03 — Progressive familial intrahepatic cholestasis
  9. 5C58.04 — Benign recurrent intrahepatic cholestasis
  10. 5C51.3 — Glycogen storage disease
  11. 5C51.4 — Disorders of galactose metabolism
    It contains 5 clarifying diagnoses.
  12. 5C51.5 — Disorders of fructose metabolism
    It contains 4 clarifying diagnoses.
  13. 5C5A — Alpha-1-antitrypsin deficiency
  14. 8E46 — Reye syndrome
  15. 5C90.Y — Other specified metabolic or transporter liver disease
  16. 5C90.Z — Metabolic or transporter liver disease, unspecified

The diagnosis is coded elsewhere:

The diagnosis is included in 8 other classes.

  • Bile acid synthesis defect with cholestasis (5C52.11)
  • Progressive familial intrahepatic cholestasis (5C58.03)
  • Benign recurrent intrahepatic cholestasis (5C58.04)
  • Glycogen storage disease (5C51.3)
  • Disorders of galactose metabolism (5C51.4)
  • Disorders of fructose metabolism (5C51.5)
  • Alpha-1-antitrypsin deficiency (5C5A)
  • Reye syndrome (8E46)

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