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:
- 5C90.0 — Liver diseases due to urea cycle defects
It contains 3 clarifying diagnoses. - 5C90.1 — Liver diseases due to disorders of porphyrin or bilirubin metabolism or transport
It contains 5 clarifying diagnoses. - 5C90.2 — Liver diseases due to disorders of amino acid metabolism
It contains 2 clarifying diagnoses. - 5C90.3 — Liver disease due to disorders of lysosomal storage
- 5C90.4 — Liver diseases due to mitochondrial disorders
- 5C90.5 — Liver diseases due to disorders of mineral metabolism
It contains 1 clarifying diagnosis. - 5C52.11 — Bile acid synthesis defect with cholestasis
- 5C58.03 — Progressive familial intrahepatic cholestasis
- 5C58.04 — Benign recurrent intrahepatic cholestasis
- 5C51.3 — Glycogen storage disease
- 5C51.4 — Disorders of galactose metabolism
It contains 5 clarifying diagnoses. - 5C51.5 — Disorders of fructose metabolism
It contains 4 clarifying diagnoses. - 5C5A — Alpha-1-antitrypsin deficiency
- 8E46 — Reye syndrome
- 5C90.Y — Other specified metabolic or transporter liver disease
- 5C90.Z — Metabolic or transporter liver disease, unspecified
The diagnosis is coded elsewhere:
- Diseases of liver #14257
- Metabolic or transporter liver disease #14401
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)