5C53.3Y

ICD-11 MMS 2026-01

Other specified disorders of mitochondrial membrane transport

Exclusions from above levels

  • http://id.who.int/icd/entity/1191191920 – Disorders of lipoprotein metabolism or certain specified lipidaemias
  • 3A10.Z – Hereditary haemolytic anaemia due to enzyme deficiency
  • 5A71.01 – Congenital adrenal hyperplasia
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  • 5A81.1 – 5-alpha-reductase deficiency
  • LD28.01 – Marfan syndrome
  • LD28.1 – Ehlers-Danlos syndrome
  • LD2A.4 – androgen resistance syndrome
  • 18 – Pregnancy, childbirth or the puerperium
  • http://id.who.int/icd/entity/1004987305 – Transitory endocrine or metabolic disorders specific to fetus or newborn

Sibling codes

  • 5C53.30 – Mitochondrial substrate carrier disorders
  • 5C53.31 – Mitochondrial protein import disorders
  • 5C53.3Z – Disorders of mitochondrial membrane transport, unspecified

Foundation entity

Disorders of mitochondrial membrane transport – http://id.who.int/icd/entity/1340308055

Part of: 5C53.3: Disorders of mitochondrial membrane transport › 5C53: Inborn errors of energy metabolism › 05: Endocrine, nutritional or metabolic diseases