5C90.4ICD-11 MMS 2026-01
Liver diseases due to mitochondrial disorders
Description
This is liver disease due to a group of disorders caused by dysfunctional mitochondria, the organelles that generate energy for the cell.
Index terms
- Liver diseases due to mitochondrial disorders
Exclusions from above levels
DB92– Non-alcoholic fatty liver diseaseDB94– Alcoholic liver diseaseDB95– Drug-induced or toxic liver disease
Show allHide
JA65.0– Acute fatty liver of pregnancy3A10.Z– Hereditary haemolytic anaemia due to enzyme deficiency5A71.01– Congenital adrenal hyperplasia5A81.1– 5-alpha-reductase deficiencyLD28.01– Marfan syndromeLD28.1– Ehlers-Danlos syndromeLD2A.4– androgen resistance syndrome18– Pregnancy, childbirth or the puerperium- http://id.who.int/icd/entity/1004987305 – Transitory endocrine or metabolic disorders specific to fetus or newborn
Sibling codes
5C90.0– Liver diseases due to urea cycle defects5C90.1– Liver diseases due to disorders of porphyrin or bilirubin metabolism or transport5C90.2– Liver diseases due to disorders of amino acid metabolism5C90.3– Liver disease due to disorders of lysosomal storage5C90.5– Liver diseases due to disorders of mineral metabolism5C90.Y– Other specified metabolic or transporter liver disease5C90.Z– Metabolic or transporter liver disease, unspecified
Foundation entity
Liver diseases due to mitochondrial disorders – http://id.who.int/icd/entity/1396810221
Allowed postcoordination axes
Part of: 5C90: Metabolic or transporter liver disease › 05: Endocrine, nutritional or metabolic diseases